U.S. flag

An official website of the United States government

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Links from Protein

Items: 1 to 20 of 360

1.

rs1489630461 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    A>G,T [Show Flanks]
    Chromosome:
    14:72518479 (GRCh38)
    14:72985187 (GRCh37)
    Canonical SPDI:
    NC_000014.9:72518478:A:G,NC_000014.9:72518478:A:T
    Gene:
    RGS6 (Varview)
    Functional Consequence:
    genic_downstream_transcript_variant,missense_variant,coding_sequence_variant,non_coding_transcript_variant,downstream_transcript_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0./0 (ALFA)
    T=0.000007/1 (GnomAD)
    T=0.000016/4 (GnomAD_exomes)
    HGVS:
    NC_000014.9:g.72518479A>G, NC_000014.9:g.72518479A>T, NC_000014.8:g.72985187A>G, NC_000014.8:g.72985187A>T, NG_029236.1:g.591371A>G, NG_029236.1:g.591371A>T, NM_004296.7:c.1220A>G, NM_004296.7:c.1220A>T, NM_004296.6:c.1220A>G, NM_004296.6:c.1220A>T, NM_004296.5:c.1220A>G, NM_004296.5:c.1220A>T, NM_001204416.3:c.1220A>G, NM_001204416.3:c.1220A>T, NM_001204416.2:c.1220A>G, NM_001204416.2:c.1220A>T, NM_001204416.1:c.1220A>G, NM_001204416.1:c.1220A>T, NM_001204419.3:c.1109A>G, NM_001204419.3:c.1109A>T, NM_001204419.2:c.1109A>G, NM_001204419.2:c.1109A>T, NM_001204419.1:c.1109A>G, NM_001204419.1:c.1109A>T, NM_001204420.3:c.1109A>G, NM_001204420.3:c.1109A>T, NM_001204420.2:c.1109A>G, NM_001204420.2:c.1109A>T, NM_001204420.1:c.1109A>G, NM_001204420.1:c.1109A>T, NM_001204417.3:c.1220A>G, NM_001204417.3:c.1220A>T, NM_001204417.2:c.1220A>G, NM_001204417.2:c.1220A>T, NM_001204417.1:c.1220A>G, NM_001204417.1:c.1220A>T, NM_001204418.3:c.1220A>G, NM_001204418.3:c.1220A>T, NM_001204418.2:c.1220A>G, NM_001204418.2:c.1220A>T, NM_001204418.1:c.1220A>G, NM_001204418.1:c.1220A>T, NM_001204421.3:c.1109A>G, NM_001204421.3:c.1109A>T, NM_001204421.2:c.1109A>G, NM_001204421.2:c.1109A>T, NM_001204421.1:c.1109A>G, NM_001204421.1:c.1109A>T, NM_001204422.3:c.1109A>G, NM_001204422.3:c.1109A>T, NM_001204422.2:c.1109A>G, NM_001204422.2:c.1109A>T, NM_001204422.1:c.1109A>G, NM_001204422.1:c.1109A>T, NM_001204424.2:c.1220A>G, NM_001204424.2:c.1220A>T, NM_001204424.1:c.1220A>G, NM_001204424.1:c.1220A>T, NR_135235.2:n.1321A>G, NR_135235.2:n.1321A>T, NR_135235.1:n.1505A>G, NR_135235.1:n.1505A>T, NM_001204423.2:c.1115A>G, NM_001204423.2:c.1115A>T, NM_001204423.1:c.1115A>G, NM_001204423.1:c.1115A>T, NM_001370282.1:c.1220A>G, NM_001370282.1:c.1220A>T, NM_001370277.1:c.1220A>G, NM_001370277.1:c.1220A>T, NM_001370273.1:c.1220A>G, NM_001370273.1:c.1220A>T, NM_001370280.1:c.1094A>G, NM_001370280.1:c.1094A>T, NM_001370291.1:c.1220A>G, NM_001370291.1:c.1220A>T, NM_001370287.1:c.1220A>G, NM_001370287.1:c.1220A>T, NM_001370275.1:c.1220A>G, NM_001370275.1:c.1220A>T, NM_001370286.1:c.1010A>G, NM_001370286.1:c.1010A>T, NM_001370292.1:c.1109A>G, NM_001370292.1:c.1109A>T, NM_001370271.1:c.1220A>G, NM_001370271.1:c.1220A>T, NM_001370284.1:c.1220A>G, NM_001370284.1:c.1220A>T, NM_001370278.1:c.1220A>G, NM_001370278.1:c.1220A>T, NM_001370294.1:c.983A>G, NM_001370294.1:c.983A>T, NM_001370288.1:c.1220A>G, NM_001370288.1:c.1220A>T, NM_001370274.1:c.1220A>G, NM_001370274.1:c.1220A>T, NM_001370279.1:c.1211A>G, NM_001370279.1:c.1211A>T, NM_001370270.1:c.1220A>G, NM_001370270.1:c.1220A>T, NM_001370290.1:c.1220A>G, NM_001370290.1:c.1220A>T, NM_001370293.1:c.1109A>G, NM_001370293.1:c.1109A>T, NM_001370272.1:c.1220A>G, NM_001370272.1:c.1220A>T, NM_001370283.1:c.1109A>G, NM_001370283.1:c.1109A>T, NM_001370276.1:c.1220A>G, NM_001370276.1:c.1220A>T, NM_001370289.1:c.1220A>G, NM_001370289.1:c.1220A>T, NM_001370281.1:c.1220A>G, NM_001370281.1:c.1220A>T, XM_017021820.3:c.1109A>G, XM_017021820.3:c.1109A>T, XM_017021820.2:c.1109A>G, XM_017021820.2:c.1109A>T, XM_017021820.1:c.1109A>G, XM_017021820.1:c.1109A>T, XM_017021826.3:c.1220A>G, XM_017021826.3:c.1220A>T, XM_017021826.2:c.1220A>G, XM_017021826.2:c.1220A>T, XM_017021826.1:c.1220A>G, XM_017021826.1:c.1220A>T, XM_017021830.3:c.1220A>G, XM_017021830.3:c.1220A>T, XM_017021830.2:c.1220A>G, XM_017021830.2:c.1220A>T, XM_017021830.1:c.1220A>G, XM_017021830.1:c.1220A>T, XM_017021832.3:c.1220A>G, XM_017021832.3:c.1220A>T, XM_017021832.2:c.1220A>G, XM_017021832.2:c.1220A>T, XM_017021832.1:c.1220A>G, XM_017021832.1:c.1220A>T, XM_017021822.3:c.1220A>G, XM_017021822.3:c.1220A>T, XM_017021822.2:c.1220A>G, XM_017021822.2:c.1220A>T, XM_017021822.1:c.1220A>G, XM_017021822.1:c.1220A>T, XM_017021827.3:c.1220A>G, XM_017021827.3:c.1220A>T, XM_017021827.2:c.1220A>G, XM_017021827.2:c.1220A>T, XM_017021827.1:c.1220A>G, XM_017021827.1:c.1220A>T, XM_017021828.3:c.1220A>G, XM_017021828.3:c.1220A>T, XM_017021828.2:c.1220A>G, XM_017021828.2:c.1220A>T, XM_017021828.1:c.1220A>G, XM_017021828.1:c.1220A>T, XM_017021825.3:c.1220A>G, XM_017021825.3:c.1220A>T, XM_017021825.2:c.1220A>G, XM_017021825.2:c.1220A>T, XM_017021825.1:c.1220A>G, XM_017021825.1:c.1220A>T, XM_017021831.3:c.1220A>G, XM_017021831.3:c.1220A>T, XM_017021831.2:c.1220A>G, XM_017021831.2:c.1220A>T, XM_017021831.1:c.1220A>G, XM_017021831.1:c.1220A>T, XM_024449761.2:c.1220A>G, XM_024449761.2:c.1220A>T, XM_024449761.1:c.1220A>G, XM_024449761.1:c.1220A>T, XM_024449759.2:c.1220A>G, XM_024449759.2:c.1220A>T, XM_024449759.1:c.1220A>G, XM_024449759.1:c.1220A>T, XM_024449764.2:c.1013A>G, XM_024449764.2:c.1013A>T, XM_024449764.1:c.1013A>G, XM_024449764.1:c.1013A>T, XM_024449776.2:c.1109A>G, XM_024449776.2:c.1109A>T, XM_024449776.1:c.1109A>G, XM_024449776.1:c.1109A>T, XM_024449760.2:c.1220A>G, XM_024449760.2:c.1220A>T, XM_024449760.1:c.1220A>G, XM_024449760.1:c.1220A>T, XM_024449763.2:c.1013A>G, XM_024449763.2:c.1013A>T, XM_024449763.1:c.1013A>G, XM_024449763.1:c.1013A>T, XM_011537397.2:c.803A>G, XM_011537397.2:c.803A>T, XM_011537397.1:c.803A>G, XM_011537397.1:c.803A>T, XM_047431985.1:c.1040A>G, XM_047431985.1:c.1040A>T, XM_047431988.1:c.578A>G, XM_047431988.1:c.578A>T, XM_047431990.1:c.1109A>G, XM_047431990.1:c.1109A>T, XM_047431987.1:c.1220A>G, XM_047431987.1:c.1220A>T, NP_004287.3:p.Tyr407Cys, NP_004287.3:p.Tyr407Phe, NP_001191345.1:p.Tyr407Cys, NP_001191345.1:p.Tyr407Phe, NP_001191348.1:p.Tyr370Cys, NP_001191348.1:p.Tyr370Phe, NP_001191349.1:p.Tyr370Cys, NP_001191349.1:p.Tyr370Phe, NP_001191346.1:p.Tyr407Cys, NP_001191346.1:p.Tyr407Phe, NP_001191347.1:p.Tyr407Cys, NP_001191347.1:p.Tyr407Phe, NP_001191350.1:p.Tyr370Cys, NP_001191350.1:p.Tyr370Phe, NP_001191351.1:p.Tyr370Cys, NP_001191351.1:p.Tyr370Phe, NP_001191353.1:p.Tyr407Cys, NP_001191353.1:p.Tyr407Phe, NP_001191352.1:p.Tyr372Cys, NP_001191352.1:p.Tyr372Phe, NP_001357211.1:p.Tyr407Cys, NP_001357211.1:p.Tyr407Phe, NP_001357206.1:p.Tyr407Cys, NP_001357206.1:p.Tyr407Phe, NP_001357202.1:p.Tyr407Cys, NP_001357202.1:p.Tyr407Phe, NP_001357209.1:p.Tyr365Cys, NP_001357209.1:p.Tyr365Phe, NP_001357220.1:p.Tyr407Cys, NP_001357220.1:p.Tyr407Phe, NP_001357216.1:p.Tyr407Cys, NP_001357216.1:p.Tyr407Phe, NP_001357204.1:p.Tyr407Cys, NP_001357204.1:p.Tyr407Phe, NP_001357215.1:p.Tyr337Cys, NP_001357215.1:p.Tyr337Phe, NP_001357221.1:p.Tyr370Cys, NP_001357221.1:p.Tyr370Phe, NP_001357200.1:p.Tyr407Cys, NP_001357200.1:p.Tyr407Phe, NP_001357213.1:p.Tyr407Cys, NP_001357213.1:p.Tyr407Phe, NP_001357207.1:p.Tyr407Cys, NP_001357207.1:p.Tyr407Phe, NP_001357223.1:p.Tyr328Cys, NP_001357223.1:p.Tyr328Phe, NP_001357217.1:p.Tyr407Cys, NP_001357217.1:p.Tyr407Phe, NP_001357203.1:p.Tyr407Cys, NP_001357203.1:p.Tyr407Phe, NP_001357208.1:p.Tyr404Cys, NP_001357208.1:p.Tyr404Phe, NP_001357199.1:p.Tyr407Cys, NP_001357199.1:p.Tyr407Phe, NP_001357219.1:p.Tyr407Cys, NP_001357219.1:p.Tyr407Phe, NP_001357222.1:p.Tyr370Cys, NP_001357222.1:p.Tyr370Phe, NP_001357201.1:p.Tyr407Cys, NP_001357201.1:p.Tyr407Phe, NP_001357212.1:p.Tyr370Cys, NP_001357212.1:p.Tyr370Phe, NP_001357205.1:p.Tyr407Cys, NP_001357205.1:p.Tyr407Phe, NP_001357218.1:p.Tyr407Cys, NP_001357218.1:p.Tyr407Phe, NP_001357210.1:p.Tyr407Cys, NP_001357210.1:p.Tyr407Phe, XP_016877309.1:p.Tyr370Cys, XP_016877309.1:p.Tyr370Phe, XP_016877315.1:p.Tyr407Cys, XP_016877315.1:p.Tyr407Phe, XP_016877319.1:p.Tyr407Cys, XP_016877319.1:p.Tyr407Phe, XP_016877321.1:p.Tyr407Cys, XP_016877321.1:p.Tyr407Phe, XP_016877311.1:p.Tyr407Cys, XP_016877311.1:p.Tyr407Phe, XP_016877316.1:p.Tyr407Cys, XP_016877316.1:p.Tyr407Phe, XP_016877317.1:p.Tyr407Cys, XP_016877317.1:p.Tyr407Phe, XP_016877314.1:p.Tyr407Cys, XP_016877314.1:p.Tyr407Phe, XP_016877320.1:p.Tyr407Cys, XP_016877320.1:p.Tyr407Phe, XP_024305529.1:p.Tyr407Cys, XP_024305529.1:p.Tyr407Phe, XP_024305527.1:p.Tyr407Cys, XP_024305527.1:p.Tyr407Phe, XP_024305532.1:p.Tyr338Cys, XP_024305532.1:p.Tyr338Phe, XP_024305544.1:p.Tyr370Cys, XP_024305544.1:p.Tyr370Phe, XP_024305528.1:p.Tyr407Cys, XP_024305528.1:p.Tyr407Phe, XP_024305531.1:p.Tyr338Cys, XP_024305531.1:p.Tyr338Phe, XP_011535699.1:p.Tyr268Cys, XP_011535699.1:p.Tyr268Phe, XP_047287941.1:p.Tyr347Cys, XP_047287941.1:p.Tyr347Phe, XP_047287944.1:p.Tyr193Cys, XP_047287944.1:p.Tyr193Phe, XP_047287946.1:p.Tyr370Cys, XP_047287946.1:p.Tyr370Phe, XP_047287943.1:p.Tyr407Cys, XP_047287943.1:p.Tyr407Phe

    2.

    rs1487449169 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      G>A [Show Flanks]
      Chromosome:
      14:72458288 (GRCh38)
      14:72924996 (GRCh37)
      Canonical SPDI:
      NC_000014.9:72458287:G:A
      Gene:
      RGS6 (Varview)
      Functional Consequence:
      5_prime_UTR_variant,genic_upstream_transcript_variant,missense_variant,upstream_transcript_variant,coding_sequence_variant,non_coding_transcript_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      A=0./0 (ALFA)
      A=0.000004/1 (TOPMED)
      HGVS:
      NC_000014.9:g.72458288G>A, NC_000014.8:g.72924996G>A, NG_029236.1:g.531180G>A, NM_004296.7:c.253G>A, NM_004296.6:c.253G>A, NM_004296.5:c.253G>A, NM_001204416.3:c.253G>A, NM_001204416.2:c.253G>A, NM_001204416.1:c.253G>A, NM_001204419.3:c.253G>A, NM_001204419.2:c.253G>A, NM_001204419.1:c.253G>A, NM_001204420.3:c.253G>A, NM_001204420.2:c.253G>A, NM_001204420.1:c.253G>A, NM_001204417.3:c.253G>A, NM_001204417.2:c.253G>A, NM_001204417.1:c.253G>A, NM_001204418.3:c.253G>A, NM_001204418.2:c.253G>A, NM_001204418.1:c.253G>A, NM_001204421.3:c.253G>A, NM_001204421.2:c.253G>A, NM_001204421.1:c.253G>A, NM_001204422.3:c.253G>A, NM_001204422.2:c.253G>A, NM_001204422.1:c.253G>A, NM_001204424.2:c.253G>A, NM_001204424.1:c.253G>A, NR_135235.2:n.354G>A, NR_135235.1:n.538G>A, NM_001204423.2:c.148G>A, NM_001204423.1:c.148G>A, NM_001370282.1:c.253G>A, NM_001370277.1:c.253G>A, NM_001370273.1:c.253G>A, NM_001370280.1:c.253G>A, NM_001370291.1:c.253G>A, NM_001370287.1:c.253G>A, NM_001370275.1:c.253G>A, NM_001370286.1:c.253G>A, NM_001370292.1:c.253G>A, NM_001370271.1:c.253G>A, NM_001370284.1:c.253G>A, NM_001370278.1:c.253G>A, NM_001370294.1:c.253G>A, NM_001370288.1:c.253G>A, NM_001370274.1:c.253G>A, NM_001370279.1:c.253G>A, NM_001370270.1:c.253G>A, NM_001370290.1:c.253G>A, NM_001370293.1:c.253G>A, NM_001370272.1:c.253G>A, NM_001370283.1:c.253G>A, NM_001370276.1:c.253G>A, NM_001370289.1:c.253G>A, NM_001370281.1:c.253G>A, XM_017021833.3:c.253G>A, XM_017021833.2:c.253G>A, XM_017021833.1:c.253G>A, XM_017021820.3:c.253G>A, XM_017021820.2:c.253G>A, XM_017021820.1:c.253G>A, XM_017021826.3:c.253G>A, XM_017021826.2:c.253G>A, XM_017021826.1:c.253G>A, XM_017021830.3:c.253G>A, XM_017021830.2:c.253G>A, XM_017021830.1:c.253G>A, XM_017021832.3:c.253G>A, XM_017021832.2:c.253G>A, XM_017021832.1:c.253G>A, XM_017021822.3:c.253G>A, XM_017021822.2:c.253G>A, XM_017021822.1:c.253G>A, XM_017021827.3:c.253G>A, XM_017021827.2:c.253G>A, XM_017021827.1:c.253G>A, XM_017021828.3:c.253G>A, XM_017021828.2:c.253G>A, XM_017021828.1:c.253G>A, XM_017021825.3:c.253G>A, XM_017021825.2:c.253G>A, XM_017021825.1:c.253G>A, XM_017021831.3:c.253G>A, XM_017021831.2:c.253G>A, XM_017021831.1:c.253G>A, XM_024449761.2:c.253G>A, XM_024449761.1:c.253G>A, XM_024449759.2:c.253G>A, XM_024449759.1:c.253G>A, XM_024449764.2:c.46G>A, XM_024449764.1:c.46G>A, XM_024449776.2:c.253G>A, XM_024449776.1:c.253G>A, XM_024449760.2:c.253G>A, XM_024449760.1:c.253G>A, XM_024449763.2:c.46G>A, XM_024449763.1:c.46G>A, XM_047431985.1:c.-64G>A, XM_047431990.1:c.253G>A, XM_047431987.1:c.253G>A, NP_004287.3:p.Gly85Arg, NP_001191345.1:p.Gly85Arg, NP_001191348.1:p.Gly85Arg, NP_001191349.1:p.Gly85Arg, NP_001191346.1:p.Gly85Arg, NP_001191347.1:p.Gly85Arg, NP_001191350.1:p.Gly85Arg, NP_001191351.1:p.Gly85Arg, NP_001191353.1:p.Gly85Arg, NP_001191352.1:p.Gly50Arg, NP_001357211.1:p.Gly85Arg, NP_001357206.1:p.Gly85Arg, NP_001357202.1:p.Gly85Arg, NP_001357209.1:p.Gly85Arg, NP_001357220.1:p.Gly85Arg, NP_001357216.1:p.Gly85Arg, NP_001357204.1:p.Gly85Arg, NP_001357215.1:p.Gly85Arg, NP_001357221.1:p.Gly85Arg, NP_001357200.1:p.Gly85Arg, NP_001357213.1:p.Gly85Arg, NP_001357207.1:p.Gly85Arg, NP_001357223.1:p.Gly85Arg, NP_001357217.1:p.Gly85Arg, NP_001357203.1:p.Gly85Arg, NP_001357208.1:p.Gly85Arg, NP_001357199.1:p.Gly85Arg, NP_001357219.1:p.Gly85Arg, NP_001357222.1:p.Gly85Arg, NP_001357201.1:p.Gly85Arg, NP_001357212.1:p.Gly85Arg, NP_001357205.1:p.Gly85Arg, NP_001357218.1:p.Gly85Arg, NP_001357210.1:p.Gly85Arg, XP_016877322.1:p.Gly85Arg, XP_016877309.1:p.Gly85Arg, XP_016877315.1:p.Gly85Arg, XP_016877319.1:p.Gly85Arg, XP_016877321.1:p.Gly85Arg, XP_016877311.1:p.Gly85Arg, XP_016877316.1:p.Gly85Arg, XP_016877317.1:p.Gly85Arg, XP_016877314.1:p.Gly85Arg, XP_016877320.1:p.Gly85Arg, XP_024305529.1:p.Gly85Arg, XP_024305527.1:p.Gly85Arg, XP_024305532.1:p.Gly16Arg, XP_024305544.1:p.Gly85Arg, XP_024305528.1:p.Gly85Arg, XP_024305531.1:p.Gly16Arg, XP_047287946.1:p.Gly85Arg, XP_047287943.1:p.Gly85Arg

      3.

      rs1487374149 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        G>A [Show Flanks]
        Chromosome:
        14:72518491 (GRCh38)
        14:72985199 (GRCh37)
        Canonical SPDI:
        NC_000014.9:72518490:G:A
        Gene:
        RGS6 (Varview)
        Functional Consequence:
        genic_downstream_transcript_variant,missense_variant,coding_sequence_variant,non_coding_transcript_variant,downstream_transcript_variant
        Validated:
        by frequency,by alfa
        MAF:
        A=0.000062/2 (ALFA)
        A=0.000004/1 (GnomAD_exomes)
        HGVS:
        NC_000014.9:g.72518491G>A, NC_000014.8:g.72985199G>A, NG_029236.1:g.591383G>A, NM_004296.7:c.1232G>A, NM_004296.6:c.1232G>A, NM_004296.5:c.1232G>A, NM_001204416.3:c.1232G>A, NM_001204416.2:c.1232G>A, NM_001204416.1:c.1232G>A, NM_001204419.3:c.1121G>A, NM_001204419.2:c.1121G>A, NM_001204419.1:c.1121G>A, NM_001204420.3:c.1121G>A, NM_001204420.2:c.1121G>A, NM_001204420.1:c.1121G>A, NM_001204417.3:c.1232G>A, NM_001204417.2:c.1232G>A, NM_001204417.1:c.1232G>A, NM_001204418.3:c.1232G>A, NM_001204418.2:c.1232G>A, NM_001204418.1:c.1232G>A, NM_001204421.3:c.1121G>A, NM_001204421.2:c.1121G>A, NM_001204421.1:c.1121G>A, NM_001204422.3:c.1121G>A, NM_001204422.2:c.1121G>A, NM_001204422.1:c.1121G>A, NM_001204424.2:c.1232G>A, NM_001204424.1:c.1232G>A, NR_135235.2:n.1333G>A, NR_135235.1:n.1517G>A, NM_001204423.2:c.1127G>A, NM_001204423.1:c.1127G>A, NM_001370282.1:c.1232G>A, NM_001370277.1:c.1232G>A, NM_001370273.1:c.1232G>A, NM_001370280.1:c.1106G>A, NM_001370291.1:c.1232G>A, NM_001370287.1:c.1232G>A, NM_001370275.1:c.1232G>A, NM_001370286.1:c.1022G>A, NM_001370292.1:c.1121G>A, NM_001370271.1:c.1232G>A, NM_001370284.1:c.1232G>A, NM_001370278.1:c.1232G>A, NM_001370294.1:c.995G>A, NM_001370288.1:c.1232G>A, NM_001370274.1:c.1232G>A, NM_001370279.1:c.1223G>A, NM_001370270.1:c.1232G>A, NM_001370290.1:c.1232G>A, NM_001370293.1:c.1121G>A, NM_001370272.1:c.1232G>A, NM_001370283.1:c.1121G>A, NM_001370276.1:c.1232G>A, NM_001370289.1:c.1232G>A, NM_001370281.1:c.1232G>A, XM_017021820.3:c.1121G>A, XM_017021820.2:c.1121G>A, XM_017021820.1:c.1121G>A, XM_017021826.3:c.1232G>A, XM_017021826.2:c.1232G>A, XM_017021826.1:c.1232G>A, XM_017021830.3:c.1232G>A, XM_017021830.2:c.1232G>A, XM_017021830.1:c.1232G>A, XM_017021832.3:c.1232G>A, XM_017021832.2:c.1232G>A, XM_017021832.1:c.1232G>A, XM_017021822.3:c.1232G>A, XM_017021822.2:c.1232G>A, XM_017021822.1:c.1232G>A, XM_017021827.3:c.1232G>A, XM_017021827.2:c.1232G>A, XM_017021827.1:c.1232G>A, XM_017021828.3:c.1232G>A, XM_017021828.2:c.1232G>A, XM_017021828.1:c.1232G>A, XM_017021825.3:c.1232G>A, XM_017021825.2:c.1232G>A, XM_017021825.1:c.1232G>A, XM_017021831.3:c.1232G>A, XM_017021831.2:c.1232G>A, XM_017021831.1:c.1232G>A, XM_024449761.2:c.1232G>A, XM_024449761.1:c.1232G>A, XM_024449759.2:c.1232G>A, XM_024449759.1:c.1232G>A, XM_024449764.2:c.1025G>A, XM_024449764.1:c.1025G>A, XM_024449776.2:c.1121G>A, XM_024449776.1:c.1121G>A, XM_024449760.2:c.1232G>A, XM_024449760.1:c.1232G>A, XM_024449763.2:c.1025G>A, XM_024449763.1:c.1025G>A, XM_011537397.2:c.815G>A, XM_011537397.1:c.815G>A, XM_047431985.1:c.1052G>A, XM_047431988.1:c.590G>A, XM_047431990.1:c.1121G>A, XM_047431987.1:c.1232G>A, NP_004287.3:p.Ser411Asn, NP_001191345.1:p.Ser411Asn, NP_001191348.1:p.Ser374Asn, NP_001191349.1:p.Ser374Asn, NP_001191346.1:p.Ser411Asn, NP_001191347.1:p.Ser411Asn, NP_001191350.1:p.Ser374Asn, NP_001191351.1:p.Ser374Asn, NP_001191353.1:p.Ser411Asn, NP_001191352.1:p.Ser376Asn, NP_001357211.1:p.Ser411Asn, NP_001357206.1:p.Ser411Asn, NP_001357202.1:p.Ser411Asn, NP_001357209.1:p.Ser369Asn, NP_001357220.1:p.Ser411Asn, NP_001357216.1:p.Ser411Asn, NP_001357204.1:p.Ser411Asn, NP_001357215.1:p.Ser341Asn, NP_001357221.1:p.Ser374Asn, NP_001357200.1:p.Ser411Asn, NP_001357213.1:p.Ser411Asn, NP_001357207.1:p.Ser411Asn, NP_001357223.1:p.Ser332Asn, NP_001357217.1:p.Ser411Asn, NP_001357203.1:p.Ser411Asn, NP_001357208.1:p.Ser408Asn, NP_001357199.1:p.Ser411Asn, NP_001357219.1:p.Ser411Asn, NP_001357222.1:p.Ser374Asn, NP_001357201.1:p.Ser411Asn, NP_001357212.1:p.Ser374Asn, NP_001357205.1:p.Ser411Asn, NP_001357218.1:p.Ser411Asn, NP_001357210.1:p.Ser411Asn, XP_016877309.1:p.Ser374Asn, XP_016877315.1:p.Ser411Asn, XP_016877319.1:p.Ser411Asn, XP_016877321.1:p.Ser411Asn, XP_016877311.1:p.Ser411Asn, XP_016877316.1:p.Ser411Asn, XP_016877317.1:p.Ser411Asn, XP_016877314.1:p.Ser411Asn, XP_016877320.1:p.Ser411Asn, XP_024305529.1:p.Ser411Asn, XP_024305527.1:p.Ser411Asn, XP_024305532.1:p.Ser342Asn, XP_024305544.1:p.Ser374Asn, XP_024305528.1:p.Ser411Asn, XP_024305531.1:p.Ser342Asn, XP_011535699.1:p.Ser272Asn, XP_047287941.1:p.Ser351Asn, XP_047287944.1:p.Ser197Asn, XP_047287946.1:p.Ser374Asn, XP_047287943.1:p.Ser411Asn

        4.

        rs1487242945 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          C>T [Show Flanks]
          Chromosome:
          14:72510163 (GRCh38)
          14:72976871 (GRCh37)
          Canonical SPDI:
          NC_000014.9:72510162:C:T
          Gene:
          RGS6 (Varview)
          Functional Consequence:
          coding_sequence_variant,intron_variant,non_coding_transcript_variant,synonymous_variant
          Validated:
          by frequency,by alfa
          MAF:
          T=0./0 (ALFA)
          HGVS:
          NC_000014.9:g.72510163C>T, NC_000014.8:g.72976871C>T, NG_029236.1:g.583055C>T, NM_004296.7:c.975C>T, NM_004296.6:c.975C>T, NM_004296.5:c.975C>T, NM_001204416.3:c.975C>T, NM_001204416.2:c.975C>T, NM_001204416.1:c.975C>T, NM_001204419.3:c.864C>T, NM_001204419.2:c.864C>T, NM_001204419.1:c.864C>T, NM_001204420.3:c.864C>T, NM_001204420.2:c.864C>T, NM_001204420.1:c.864C>T, NM_001204417.3:c.975C>T, NM_001204417.2:c.975C>T, NM_001204417.1:c.975C>T, NM_001204418.3:c.975C>T, NM_001204418.2:c.975C>T, NM_001204418.1:c.975C>T, NM_001204421.3:c.864C>T, NM_001204421.2:c.864C>T, NM_001204421.1:c.864C>T, NM_001204422.3:c.864C>T, NM_001204422.2:c.864C>T, NM_001204422.1:c.864C>T, NM_001204424.2:c.975C>T, NM_001204424.1:c.975C>T, NR_135235.2:n.1076C>T, NR_135235.1:n.1260C>T, NM_001204423.2:c.870C>T, NM_001204423.1:c.870C>T, NM_001370282.1:c.975C>T, NM_001370277.1:c.975C>T, NM_001370273.1:c.975C>T, NM_001370291.1:c.975C>T, NM_001370287.1:c.975C>T, NM_001370275.1:c.975C>T, NM_001370286.1:c.765C>T, NM_001370292.1:c.864C>T, NM_001370271.1:c.975C>T, NM_001370284.1:c.975C>T, NM_001370278.1:c.975C>T, NM_001370288.1:c.975C>T, NM_001370274.1:c.975C>T, NM_001370279.1:c.966C>T, NM_001370270.1:c.975C>T, NM_001370290.1:c.975C>T, NM_001370293.1:c.864C>T, NM_001370272.1:c.975C>T, NM_001370283.1:c.864C>T, NM_001370276.1:c.975C>T, NM_001370289.1:c.975C>T, NM_001370281.1:c.975C>T, XM_017021833.3:c.975C>T, XM_017021833.2:c.975C>T, XM_017021833.1:c.975C>T, XM_017021820.3:c.864C>T, XM_017021820.2:c.864C>T, XM_017021820.1:c.864C>T, XM_017021826.3:c.975C>T, XM_017021826.2:c.975C>T, XM_017021826.1:c.975C>T, XM_017021830.3:c.975C>T, XM_017021830.2:c.975C>T, XM_017021830.1:c.975C>T, XM_017021832.3:c.975C>T, XM_017021832.2:c.975C>T, XM_017021832.1:c.975C>T, XM_017021822.3:c.975C>T, XM_017021822.2:c.975C>T, XM_017021822.1:c.975C>T, XM_017021827.3:c.975C>T, XM_017021827.2:c.975C>T, XM_017021827.1:c.975C>T, XM_017021828.3:c.975C>T, XM_017021828.2:c.975C>T, XM_017021828.1:c.975C>T, XM_017021825.3:c.975C>T, XM_017021825.2:c.975C>T, XM_017021825.1:c.975C>T, XM_017021831.3:c.975C>T, XM_017021831.2:c.975C>T, XM_017021831.1:c.975C>T, XM_024449761.2:c.975C>T, XM_024449761.1:c.975C>T, XM_024449759.2:c.975C>T, XM_024449759.1:c.975C>T, XM_024449764.2:c.768C>T, XM_024449764.1:c.768C>T, XM_024449776.2:c.864C>T, XM_024449776.1:c.864C>T, XM_024449760.2:c.975C>T, XM_024449760.1:c.975C>T, XM_024449763.2:c.768C>T, XM_024449763.1:c.768C>T, XM_011537397.2:c.558C>T, XM_011537397.1:c.558C>T, XM_047431985.1:c.795C>T, XM_047431988.1:c.333C>T, XM_047431990.1:c.864C>T, XM_047431987.1:c.975C>T

          5.

          rs1484364013 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            T>C [Show Flanks]
            Chromosome:
            14:72510207 (GRCh38)
            14:72976915 (GRCh37)
            Canonical SPDI:
            NC_000014.9:72510206:T:C
            Gene:
            RGS6 (Varview)
            Functional Consequence:
            coding_sequence_variant,intron_variant,non_coding_transcript_variant,missense_variant
            Validated:
            by frequency
            MAF:
            C=0.000004/1 (GnomAD_exomes)
            HGVS:
            NC_000014.9:g.72510207T>C, NC_000014.8:g.72976915T>C, NG_029236.1:g.583099T>C, NM_004296.7:c.1019T>C, NM_004296.6:c.1019T>C, NM_004296.5:c.1019T>C, NM_001204416.3:c.1019T>C, NM_001204416.2:c.1019T>C, NM_001204416.1:c.1019T>C, NM_001204419.3:c.908T>C, NM_001204419.2:c.908T>C, NM_001204419.1:c.908T>C, NM_001204420.3:c.908T>C, NM_001204420.2:c.908T>C, NM_001204420.1:c.908T>C, NM_001204417.3:c.1019T>C, NM_001204417.2:c.1019T>C, NM_001204417.1:c.1019T>C, NM_001204418.3:c.1019T>C, NM_001204418.2:c.1019T>C, NM_001204418.1:c.1019T>C, NM_001204421.3:c.908T>C, NM_001204421.2:c.908T>C, NM_001204421.1:c.908T>C, NM_001204422.3:c.908T>C, NM_001204422.2:c.908T>C, NM_001204422.1:c.908T>C, NM_001204424.2:c.1019T>C, NM_001204424.1:c.1019T>C, NR_135235.2:n.1120T>C, NR_135235.1:n.1304T>C, NM_001204423.2:c.914T>C, NM_001204423.1:c.914T>C, NM_001370282.1:c.1019T>C, NM_001370277.1:c.1019T>C, NM_001370273.1:c.1019T>C, NM_001370291.1:c.1019T>C, NM_001370287.1:c.1019T>C, NM_001370275.1:c.1019T>C, NM_001370286.1:c.809T>C, NM_001370292.1:c.908T>C, NM_001370271.1:c.1019T>C, NM_001370284.1:c.1019T>C, NM_001370278.1:c.1019T>C, NM_001370288.1:c.1019T>C, NM_001370274.1:c.1019T>C, NM_001370279.1:c.1010T>C, NM_001370270.1:c.1019T>C, NM_001370290.1:c.1019T>C, NM_001370293.1:c.908T>C, NM_001370272.1:c.1019T>C, NM_001370283.1:c.908T>C, NM_001370276.1:c.1019T>C, NM_001370289.1:c.1019T>C, NM_001370281.1:c.1019T>C, XM_017021833.3:c.1019T>C, XM_017021833.2:c.1019T>C, XM_017021833.1:c.1019T>C, XM_017021820.3:c.908T>C, XM_017021820.2:c.908T>C, XM_017021820.1:c.908T>C, XM_017021826.3:c.1019T>C, XM_017021826.2:c.1019T>C, XM_017021826.1:c.1019T>C, XM_017021830.3:c.1019T>C, XM_017021830.2:c.1019T>C, XM_017021830.1:c.1019T>C, XM_017021832.3:c.1019T>C, XM_017021832.2:c.1019T>C, XM_017021832.1:c.1019T>C, XM_017021822.3:c.1019T>C, XM_017021822.2:c.1019T>C, XM_017021822.1:c.1019T>C, XM_017021827.3:c.1019T>C, XM_017021827.2:c.1019T>C, XM_017021827.1:c.1019T>C, XM_017021828.3:c.1019T>C, XM_017021828.2:c.1019T>C, XM_017021828.1:c.1019T>C, XM_017021825.3:c.1019T>C, XM_017021825.2:c.1019T>C, XM_017021825.1:c.1019T>C, XM_017021831.3:c.1019T>C, XM_017021831.2:c.1019T>C, XM_017021831.1:c.1019T>C, XM_024449761.2:c.1019T>C, XM_024449761.1:c.1019T>C, XM_024449759.2:c.1019T>C, XM_024449759.1:c.1019T>C, XM_024449764.2:c.812T>C, XM_024449764.1:c.812T>C, XM_024449776.2:c.908T>C, XM_024449776.1:c.908T>C, XM_024449760.2:c.1019T>C, XM_024449760.1:c.1019T>C, XM_024449763.2:c.812T>C, XM_024449763.1:c.812T>C, XM_011537397.2:c.602T>C, XM_011537397.1:c.602T>C, XM_047431985.1:c.839T>C, XM_047431988.1:c.377T>C, XM_047431990.1:c.908T>C, XM_047431987.1:c.1019T>C, NP_004287.3:p.Ile340Thr, NP_001191345.1:p.Ile340Thr, NP_001191348.1:p.Ile303Thr, NP_001191349.1:p.Ile303Thr, NP_001191346.1:p.Ile340Thr, NP_001191347.1:p.Ile340Thr, NP_001191350.1:p.Ile303Thr, NP_001191351.1:p.Ile303Thr, NP_001191353.1:p.Ile340Thr, NP_001191352.1:p.Ile305Thr, NP_001357211.1:p.Ile340Thr, NP_001357206.1:p.Ile340Thr, NP_001357202.1:p.Ile340Thr, NP_001357220.1:p.Ile340Thr, NP_001357216.1:p.Ile340Thr, NP_001357204.1:p.Ile340Thr, NP_001357215.1:p.Ile270Thr, NP_001357221.1:p.Ile303Thr, NP_001357200.1:p.Ile340Thr, NP_001357213.1:p.Ile340Thr, NP_001357207.1:p.Ile340Thr, NP_001357217.1:p.Ile340Thr, NP_001357203.1:p.Ile340Thr, NP_001357208.1:p.Ile337Thr, NP_001357199.1:p.Ile340Thr, NP_001357219.1:p.Ile340Thr, NP_001357222.1:p.Ile303Thr, NP_001357201.1:p.Ile340Thr, NP_001357212.1:p.Ile303Thr, NP_001357205.1:p.Ile340Thr, NP_001357218.1:p.Ile340Thr, NP_001357210.1:p.Ile340Thr, XP_016877322.1:p.Ile340Thr, XP_016877309.1:p.Ile303Thr, XP_016877315.1:p.Ile340Thr, XP_016877319.1:p.Ile340Thr, XP_016877321.1:p.Ile340Thr, XP_016877311.1:p.Ile340Thr, XP_016877316.1:p.Ile340Thr, XP_016877317.1:p.Ile340Thr, XP_016877314.1:p.Ile340Thr, XP_016877320.1:p.Ile340Thr, XP_024305529.1:p.Ile340Thr, XP_024305527.1:p.Ile340Thr, XP_024305532.1:p.Ile271Thr, XP_024305544.1:p.Ile303Thr, XP_024305528.1:p.Ile340Thr, XP_024305531.1:p.Ile271Thr, XP_011535699.1:p.Ile201Thr, XP_047287941.1:p.Ile280Thr, XP_047287944.1:p.Ile126Thr, XP_047287946.1:p.Ile303Thr, XP_047287943.1:p.Ile340Thr

            6.

            rs1478594532 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              C>G,T [Show Flanks]
              Chromosome:
              14:72540059 (GRCh38)
              14:73006767 (GRCh37)
              Canonical SPDI:
              NC_000014.9:72540058:C:G,NC_000014.9:72540058:C:T
              Gene:
              RGS6 (Varview)
              Functional Consequence:
              synonymous_variant,genic_downstream_transcript_variant,missense_variant,coding_sequence_variant,intron_variant,non_coding_transcript_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              T=0./0 (ALFA)
              G=0.000005/1 (GnomAD_exomes)
              T=0.000014/2 (GnomAD)
              HGVS:
              NC_000014.9:g.72540059C>G, NC_000014.9:g.72540059C>T, NC_000014.8:g.73006767C>G, NC_000014.8:g.73006767C>T, NG_029236.1:g.612951C>G, NG_029236.1:g.612951C>T, NM_001204416.3:c.1387C>G, NM_001204416.3:c.1387C>T, NM_001204416.2:c.1387C>G, NM_001204416.2:c.1387C>T, NM_001204416.1:c.1387C>G, NM_001204416.1:c.1387C>T, NM_001204419.3:c.1276C>G, NM_001204419.3:c.1276C>T, NM_001204419.2:c.1276C>G, NM_001204419.2:c.1276C>T, NM_001204419.1:c.1276C>G, NM_001204419.1:c.1276C>T, NM_001204417.3:c.1387C>G, NM_001204417.3:c.1387C>T, NM_001204417.2:c.1387C>G, NM_001204417.2:c.1387C>T, NM_001204417.1:c.1387C>G, NM_001204417.1:c.1387C>T, NM_001204421.3:c.1276C>G, NM_001204421.3:c.1276C>T, NM_001204421.2:c.1276C>G, NM_001204421.2:c.1276C>T, NM_001204421.1:c.1276C>G, NM_001204421.1:c.1276C>T, NM_001204424.2:c.1387C>G, NM_001204424.2:c.1387C>T, NM_001204424.1:c.1387C>G, NM_001204424.1:c.1387C>T, NR_135235.2:n.1484C>G, NR_135235.2:n.1484C>T, NR_135235.1:n.1668C>G, NR_135235.1:n.1668C>T, NM_001370282.1:c.1387C>G, NM_001370282.1:c.1387C>T, NM_001370277.1:c.1387C>G, NM_001370277.1:c.1387C>T, NM_001370273.1:c.1387C>G, NM_001370273.1:c.1387C>T, NM_001370280.1:c.1261C>G, NM_001370280.1:c.1261C>T, NM_001370291.1:c.1383C>G, NM_001370291.1:c.1383C>T, NM_001370275.1:c.1387C>G, NM_001370275.1:c.1387C>T, NM_001370286.1:c.1177C>G, NM_001370286.1:c.1177C>T, NM_001370271.1:c.1387C>G, NM_001370271.1:c.1387C>T, NM_001370284.1:c.1387C>G, NM_001370284.1:c.1387C>T, NM_001370278.1:c.1387C>G, NM_001370278.1:c.1387C>T, NM_001370274.1:c.1387C>G, NM_001370274.1:c.1387C>T, NM_001370279.1:c.1378C>G, NM_001370279.1:c.1378C>T, NM_001370270.1:c.1387C>G, NM_001370270.1:c.1387C>T, NM_001370290.1:c.1383C>G, NM_001370290.1:c.1383C>T, NM_001370272.1:c.1387C>G, NM_001370272.1:c.1387C>T, NM_001370283.1:c.1276C>G, NM_001370283.1:c.1276C>T, NM_001370276.1:c.1387C>G, NM_001370276.1:c.1387C>T, NM_001370281.1:c.1387C>G, NM_001370281.1:c.1387C>T, XM_017021820.3:c.1276C>G, XM_017021820.3:c.1276C>T, XM_017021820.2:c.1276C>G, XM_017021820.2:c.1276C>T, XM_017021820.1:c.1276C>G, XM_017021820.1:c.1276C>T, XM_017021826.3:c.1387C>G, XM_017021826.3:c.1387C>T, XM_017021826.2:c.1387C>G, XM_017021826.2:c.1387C>T, XM_017021826.1:c.1387C>G, XM_017021826.1:c.1387C>T, XM_017021830.3:c.1383C>G, XM_017021830.3:c.1383C>T, XM_017021830.2:c.1383C>G, XM_017021830.2:c.1383C>T, XM_017021830.1:c.1383C>G, XM_017021830.1:c.1383C>T, XM_017021822.3:c.1387C>G, XM_017021822.3:c.1387C>T, XM_017021822.2:c.1387C>G, XM_017021822.2:c.1387C>T, XM_017021822.1:c.1387C>G, XM_017021822.1:c.1387C>T, XM_017021827.3:c.1387C>G, XM_017021827.3:c.1387C>T, XM_017021827.2:c.1387C>G, XM_017021827.2:c.1387C>T, XM_017021827.1:c.1387C>G, XM_017021827.1:c.1387C>T, XM_017021825.3:c.1387C>G, XM_017021825.3:c.1387C>T, XM_017021825.2:c.1387C>G, XM_017021825.2:c.1387C>T, XM_017021825.1:c.1387C>G, XM_017021825.1:c.1387C>T, XM_024449761.2:c.1387C>G, XM_024449761.2:c.1387C>T, XM_024449761.1:c.1387C>G, XM_024449761.1:c.1387C>T, XM_024449759.2:c.1387C>G, XM_024449759.2:c.1387C>T, XM_024449759.1:c.1387C>G, XM_024449759.1:c.1387C>T, XM_024449764.2:c.1180C>G, XM_024449764.2:c.1180C>T, XM_024449764.1:c.1180C>G, XM_024449764.1:c.1180C>T, XM_024449776.2:c.1276C>G, XM_024449776.2:c.1276C>T, XM_024449776.1:c.1276C>G, XM_024449776.1:c.1276C>T, XM_024449760.2:c.1387C>G, XM_024449760.2:c.1387C>T, XM_024449760.1:c.1387C>G, XM_024449760.1:c.1387C>T, XM_024449763.2:c.1180C>G, XM_024449763.2:c.1180C>T, XM_024449763.1:c.1180C>G, XM_024449763.1:c.1180C>T, XM_011537397.2:c.970C>G, XM_011537397.2:c.970C>T, XM_011537397.1:c.970C>G, XM_011537397.1:c.970C>T, XM_047431985.1:c.1207C>G, XM_047431985.1:c.1207C>T, XM_047431988.1:c.745C>G, XM_047431988.1:c.745C>T, XM_047431987.1:c.1387C>G, XM_047431987.1:c.1387C>T, NP_001191345.1:p.Arg463Gly, NP_001191345.1:p.Arg463Cys, NP_001191348.1:p.Arg426Gly, NP_001191348.1:p.Arg426Cys, NP_001191346.1:p.Arg463Gly, NP_001191346.1:p.Arg463Cys, NP_001191350.1:p.Arg426Gly, NP_001191350.1:p.Arg426Cys, NP_001191353.1:p.Arg463Gly, NP_001191353.1:p.Arg463Cys, NP_001357211.1:p.Arg463Gly, NP_001357211.1:p.Arg463Cys, NP_001357206.1:p.Arg463Gly, NP_001357206.1:p.Arg463Cys, NP_001357202.1:p.Arg463Gly, NP_001357202.1:p.Arg463Cys, NP_001357209.1:p.Arg421Gly, NP_001357209.1:p.Arg421Cys, NP_001357204.1:p.Arg463Gly, NP_001357204.1:p.Arg463Cys, NP_001357215.1:p.Arg393Gly, NP_001357215.1:p.Arg393Cys, NP_001357200.1:p.Arg463Gly, NP_001357200.1:p.Arg463Cys, NP_001357213.1:p.Arg463Gly, NP_001357213.1:p.Arg463Cys, NP_001357207.1:p.Arg463Gly, NP_001357207.1:p.Arg463Cys, NP_001357203.1:p.Arg463Gly, NP_001357203.1:p.Arg463Cys, NP_001357208.1:p.Arg460Gly, NP_001357208.1:p.Arg460Cys, NP_001357199.1:p.Arg463Gly, NP_001357199.1:p.Arg463Cys, NP_001357201.1:p.Arg463Gly, NP_001357201.1:p.Arg463Cys, NP_001357212.1:p.Arg426Gly, NP_001357212.1:p.Arg426Cys, NP_001357205.1:p.Arg463Gly, NP_001357205.1:p.Arg463Cys, NP_001357210.1:p.Arg463Gly, NP_001357210.1:p.Arg463Cys, XP_016877309.1:p.Arg426Gly, XP_016877309.1:p.Arg426Cys, XP_016877315.1:p.Arg463Gly, XP_016877315.1:p.Arg463Cys, XP_016877311.1:p.Arg463Gly, XP_016877311.1:p.Arg463Cys, XP_016877316.1:p.Arg463Gly, XP_016877316.1:p.Arg463Cys, XP_016877314.1:p.Arg463Gly, XP_016877314.1:p.Arg463Cys, XP_024305529.1:p.Arg463Gly, XP_024305529.1:p.Arg463Cys, XP_024305527.1:p.Arg463Gly, XP_024305527.1:p.Arg463Cys, XP_024305532.1:p.Arg394Gly, XP_024305532.1:p.Arg394Cys, XP_024305544.1:p.Arg426Gly, XP_024305544.1:p.Arg426Cys, XP_024305528.1:p.Arg463Gly, XP_024305528.1:p.Arg463Cys, XP_024305531.1:p.Arg394Gly, XP_024305531.1:p.Arg394Cys, XP_011535699.1:p.Arg324Gly, XP_011535699.1:p.Arg324Cys, XP_047287941.1:p.Arg403Gly, XP_047287941.1:p.Arg403Cys, XP_047287944.1:p.Arg249Gly, XP_047287944.1:p.Arg249Cys, XP_047287943.1:p.Arg463Gly, XP_047287943.1:p.Arg463Cys

              7.

              rs1476849714 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                C>T [Show Flanks]
                Chromosome:
                14:72352190 (GRCh38)
                14:72818898 (GRCh37)
                Canonical SPDI:
                NC_000014.9:72352189:C:T
                Gene:
                RGS6 (Varview)
                Functional Consequence:
                synonymous_variant,non_coding_transcript_variant,genic_upstream_transcript_variant,coding_sequence_variant
                Validated:
                by frequency,by cluster
                MAF:
                T=0.000007/1 (GnomAD)
                HGVS:
                NC_000014.9:g.72352190C>T, NC_000014.8:g.72818898C>T, NG_029236.1:g.425082C>T, NM_004296.7:c.180C>T, NM_004296.6:c.180C>T, NM_004296.5:c.180C>T, NM_001204416.3:c.180C>T, NM_001204416.2:c.180C>T, NM_001204416.1:c.180C>T, NM_001204419.3:c.180C>T, NM_001204419.2:c.180C>T, NM_001204419.1:c.180C>T, NM_001204420.3:c.180C>T, NM_001204420.2:c.180C>T, NM_001204420.1:c.180C>T, NM_001204417.3:c.180C>T, NM_001204417.2:c.180C>T, NM_001204417.1:c.180C>T, NM_001204418.3:c.180C>T, NM_001204418.2:c.180C>T, NM_001204418.1:c.180C>T, NM_001204421.3:c.180C>T, NM_001204421.2:c.180C>T, NM_001204421.1:c.180C>T, NM_001204422.3:c.180C>T, NM_001204422.2:c.180C>T, NM_001204422.1:c.180C>T, NM_001204424.2:c.180C>T, NM_001204424.1:c.180C>T, NR_135235.2:n.281C>T, NR_135235.1:n.465C>T, NM_001204423.2:c.75C>T, NM_001204423.1:c.75C>T, NM_001370282.1:c.180C>T, NM_001370277.1:c.180C>T, NM_001370273.1:c.180C>T, NM_001370280.1:c.180C>T, NM_001370291.1:c.180C>T, NM_001370287.1:c.180C>T, NM_001370275.1:c.180C>T, NM_001370286.1:c.180C>T, NM_001370292.1:c.180C>T, NM_001370271.1:c.180C>T, NM_001370284.1:c.180C>T, NM_001370278.1:c.180C>T, NM_001370294.1:c.180C>T, NM_001370288.1:c.180C>T, NM_001370274.1:c.180C>T, NM_001370279.1:c.180C>T, NM_001370270.1:c.180C>T, NM_001370290.1:c.180C>T, NM_001370293.1:c.180C>T, NM_001370272.1:c.180C>T, NM_001370283.1:c.180C>T, NM_001370276.1:c.180C>T, NM_001370289.1:c.180C>T, NM_001370281.1:c.180C>T, XM_017021833.3:c.180C>T, XM_017021833.2:c.180C>T, XM_017021833.1:c.180C>T, XM_017021820.3:c.180C>T, XM_017021820.2:c.180C>T, XM_017021820.1:c.180C>T, XM_017021826.3:c.180C>T, XM_017021826.2:c.180C>T, XM_017021826.1:c.180C>T, XM_017021830.3:c.180C>T, XM_017021830.2:c.180C>T, XM_017021830.1:c.180C>T, XM_017021832.3:c.180C>T, XM_017021832.2:c.180C>T, XM_017021832.1:c.180C>T, XM_017021822.3:c.180C>T, XM_017021822.2:c.180C>T, XM_017021822.1:c.180C>T, XM_017021827.3:c.180C>T, XM_017021827.2:c.180C>T, XM_017021827.1:c.180C>T, XM_017021828.3:c.180C>T, XM_017021828.2:c.180C>T, XM_017021828.1:c.180C>T, XM_017021825.3:c.180C>T, XM_017021825.2:c.180C>T, XM_017021825.1:c.180C>T, XM_017021831.3:c.180C>T, XM_017021831.2:c.180C>T, XM_017021831.1:c.180C>T, XM_024449761.2:c.180C>T, XM_024449761.1:c.180C>T, XM_024449759.2:c.180C>T, XM_024449759.1:c.180C>T, XM_024449776.2:c.180C>T, XM_024449776.1:c.180C>T, XM_024449760.2:c.180C>T, XM_024449760.1:c.180C>T, XM_047431990.1:c.180C>T, XM_047431987.1:c.180C>T

                8.

                rs1475594542 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  T>C [Show Flanks]
                  Chromosome:
                  14:72465763 (GRCh38)
                  14:72932471 (GRCh37)
                  Canonical SPDI:
                  NC_000014.9:72465762:T:C
                  Gene:
                  RGS6 (Varview)
                  Functional Consequence:
                  coding_sequence_variant,missense_variant,genic_upstream_transcript_variant,non_coding_transcript_variant,5_prime_UTR_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  C=0.000224/1 (ALFA)
                  C=0.000004/1 (GnomAD_exomes)
                  C=0.000223/1 (Estonian)
                  HGVS:
                  NC_000014.9:g.72465763T>C, NC_000014.8:g.72932471T>C, NG_029236.1:g.538655T>C, NM_004296.7:c.400T>C, NM_004296.6:c.400T>C, NM_004296.5:c.400T>C, NM_001204416.3:c.400T>C, NM_001204416.2:c.400T>C, NM_001204416.1:c.400T>C, NM_001204419.3:c.400T>C, NM_001204419.2:c.400T>C, NM_001204419.1:c.400T>C, NM_001204420.3:c.400T>C, NM_001204420.2:c.400T>C, NM_001204420.1:c.400T>C, NM_001204417.3:c.400T>C, NM_001204417.2:c.400T>C, NM_001204417.1:c.400T>C, NM_001204418.3:c.400T>C, NM_001204418.2:c.400T>C, NM_001204418.1:c.400T>C, NM_001204421.3:c.400T>C, NM_001204421.2:c.400T>C, NM_001204421.1:c.400T>C, NM_001204422.3:c.400T>C, NM_001204422.2:c.400T>C, NM_001204422.1:c.400T>C, NM_001204424.2:c.400T>C, NM_001204424.1:c.400T>C, NR_135235.2:n.501T>C, NR_135235.1:n.685T>C, NM_001204423.2:c.295T>C, NM_001204423.1:c.295T>C, NM_001370282.1:c.400T>C, NM_001370277.1:c.400T>C, NM_001370273.1:c.400T>C, NM_001370280.1:c.400T>C, NM_001370291.1:c.400T>C, NM_001370287.1:c.400T>C, NM_001370275.1:c.400T>C, NM_001370286.1:c.400T>C, NM_001370292.1:c.400T>C, NM_001370271.1:c.400T>C, NM_001370284.1:c.400T>C, NM_001370278.1:c.400T>C, NM_001370294.1:c.400T>C, NM_001370288.1:c.400T>C, NM_001370274.1:c.400T>C, NM_001370279.1:c.400T>C, NM_001370270.1:c.400T>C, NM_001370290.1:c.400T>C, NM_001370293.1:c.400T>C, NM_001370272.1:c.400T>C, NM_001370283.1:c.400T>C, NM_001370276.1:c.400T>C, NM_001370289.1:c.400T>C, NM_001370281.1:c.400T>C, XM_017021833.3:c.400T>C, XM_017021833.2:c.400T>C, XM_017021833.1:c.400T>C, XM_017021820.3:c.400T>C, XM_017021820.2:c.400T>C, XM_017021820.1:c.400T>C, XM_017021826.3:c.400T>C, XM_017021826.2:c.400T>C, XM_017021826.1:c.400T>C, XM_017021830.3:c.400T>C, XM_017021830.2:c.400T>C, XM_017021830.1:c.400T>C, XM_017021832.3:c.400T>C, XM_017021832.2:c.400T>C, XM_017021832.1:c.400T>C, XM_017021822.3:c.400T>C, XM_017021822.2:c.400T>C, XM_017021822.1:c.400T>C, XM_017021827.3:c.400T>C, XM_017021827.2:c.400T>C, XM_017021827.1:c.400T>C, XM_017021828.3:c.400T>C, XM_017021828.2:c.400T>C, XM_017021828.1:c.400T>C, XM_017021825.3:c.400T>C, XM_017021825.2:c.400T>C, XM_017021825.1:c.400T>C, XM_017021831.3:c.400T>C, XM_017021831.2:c.400T>C, XM_017021831.1:c.400T>C, XM_024449761.2:c.400T>C, XM_024449761.1:c.400T>C, XM_024449759.2:c.400T>C, XM_024449759.1:c.400T>C, XM_024449764.2:c.193T>C, XM_024449764.1:c.193T>C, XM_024449776.2:c.400T>C, XM_024449776.1:c.400T>C, XM_024449760.2:c.400T>C, XM_024449760.1:c.400T>C, XM_024449763.2:c.193T>C, XM_024449763.1:c.193T>C, XM_011537397.2:c.-18T>C, XM_011537397.1:c.-18T>C, XM_047431985.1:c.220T>C, XM_047431990.1:c.400T>C, XM_047431987.1:c.400T>C, NP_004287.3:p.Tyr134His, NP_001191345.1:p.Tyr134His, NP_001191348.1:p.Tyr134His, NP_001191349.1:p.Tyr134His, NP_001191346.1:p.Tyr134His, NP_001191347.1:p.Tyr134His, NP_001191350.1:p.Tyr134His, NP_001191351.1:p.Tyr134His, NP_001191353.1:p.Tyr134His, NP_001191352.1:p.Tyr99His, NP_001357211.1:p.Tyr134His, NP_001357206.1:p.Tyr134His, NP_001357202.1:p.Tyr134His, NP_001357209.1:p.Tyr134His, NP_001357220.1:p.Tyr134His, NP_001357216.1:p.Tyr134His, NP_001357204.1:p.Tyr134His, NP_001357215.1:p.Tyr134His, NP_001357221.1:p.Tyr134His, NP_001357200.1:p.Tyr134His, NP_001357213.1:p.Tyr134His, NP_001357207.1:p.Tyr134His, NP_001357223.1:p.Tyr134His, NP_001357217.1:p.Tyr134His, NP_001357203.1:p.Tyr134His, NP_001357208.1:p.Tyr134His, NP_001357199.1:p.Tyr134His, NP_001357219.1:p.Tyr134His, NP_001357222.1:p.Tyr134His, NP_001357201.1:p.Tyr134His, NP_001357212.1:p.Tyr134His, NP_001357205.1:p.Tyr134His, NP_001357218.1:p.Tyr134His, NP_001357210.1:p.Tyr134His, XP_016877322.1:p.Tyr134His, XP_016877309.1:p.Tyr134His, XP_016877315.1:p.Tyr134His, XP_016877319.1:p.Tyr134His, XP_016877321.1:p.Tyr134His, XP_016877311.1:p.Tyr134His, XP_016877316.1:p.Tyr134His, XP_016877317.1:p.Tyr134His, XP_016877314.1:p.Tyr134His, XP_016877320.1:p.Tyr134His, XP_024305529.1:p.Tyr134His, XP_024305527.1:p.Tyr134His, XP_024305532.1:p.Tyr65His, XP_024305544.1:p.Tyr134His, XP_024305528.1:p.Tyr134His, XP_024305531.1:p.Tyr65His, XP_047287941.1:p.Tyr74His, XP_047287946.1:p.Tyr134His, XP_047287943.1:p.Tyr134His

                  9.

                  rs1473908278 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    G>T [Show Flanks]
                    Chromosome:
                    14:72472872 (GRCh38)
                    14:72939580 (GRCh37)
                    Canonical SPDI:
                    NC_000014.9:72472871:G:T
                    Gene:
                    RGS6 (Varview)
                    Functional Consequence:
                    coding_sequence_variant,missense_variant,genic_upstream_transcript_variant,non_coding_transcript_variant,upstream_transcript_variant
                    Validated:
                    by frequency,by alfa
                    MAF:
                    T=0.000111/1 (ALFA)
                    T=0.000004/1 (GnomAD_exomes)
                    HGVS:
                    NC_000014.9:g.72472872G>T, NC_000014.8:g.72939580G>T, NG_029236.1:g.545764G>T, NM_004296.7:c.537G>T, NM_004296.6:c.537G>T, NM_004296.5:c.537G>T, NM_001204416.3:c.537G>T, NM_001204416.2:c.537G>T, NM_001204416.1:c.537G>T, NM_001204419.3:c.537G>T, NM_001204419.2:c.537G>T, NM_001204419.1:c.537G>T, NM_001204420.3:c.537G>T, NM_001204420.2:c.537G>T, NM_001204420.1:c.537G>T, NM_001204417.3:c.537G>T, NM_001204417.2:c.537G>T, NM_001204417.1:c.537G>T, NM_001204418.3:c.537G>T, NM_001204418.2:c.537G>T, NM_001204418.1:c.537G>T, NM_001204421.3:c.537G>T, NM_001204421.2:c.537G>T, NM_001204421.1:c.537G>T, NM_001204422.3:c.537G>T, NM_001204422.2:c.537G>T, NM_001204422.1:c.537G>T, NM_001204424.2:c.537G>T, NM_001204424.1:c.537G>T, NR_135235.2:n.638G>T, NR_135235.1:n.822G>T, NM_001204423.2:c.432G>T, NM_001204423.1:c.432G>T, NM_001370282.1:c.537G>T, NM_001370277.1:c.537G>T, NM_001370273.1:c.537G>T, NM_001370280.1:c.537G>T, NM_001370291.1:c.537G>T, NM_001370287.1:c.537G>T, NM_001370275.1:c.537G>T, NM_001370286.1:c.537G>T, NM_001370292.1:c.537G>T, NM_001370271.1:c.537G>T, NM_001370284.1:c.537G>T, NM_001370278.1:c.537G>T, NM_001370294.1:c.537G>T, NM_001370288.1:c.537G>T, NM_001370274.1:c.537G>T, NM_001370279.1:c.537G>T, NM_001370270.1:c.537G>T, NM_001370290.1:c.537G>T, NM_001370293.1:c.537G>T, NM_001370272.1:c.537G>T, NM_001370283.1:c.537G>T, NM_001370276.1:c.537G>T, NM_001370289.1:c.537G>T, NM_001370281.1:c.537G>T, XM_017021833.3:c.537G>T, XM_017021833.2:c.537G>T, XM_017021833.1:c.537G>T, XM_017021820.3:c.537G>T, XM_017021820.2:c.537G>T, XM_017021820.1:c.537G>T, XM_017021826.3:c.537G>T, XM_017021826.2:c.537G>T, XM_017021826.1:c.537G>T, XM_017021830.3:c.537G>T, XM_017021830.2:c.537G>T, XM_017021830.1:c.537G>T, XM_017021832.3:c.537G>T, XM_017021832.2:c.537G>T, XM_017021832.1:c.537G>T, XM_017021822.3:c.537G>T, XM_017021822.2:c.537G>T, XM_017021822.1:c.537G>T, XM_017021827.3:c.537G>T, XM_017021827.2:c.537G>T, XM_017021827.1:c.537G>T, XM_017021828.3:c.537G>T, XM_017021828.2:c.537G>T, XM_017021828.1:c.537G>T, XM_017021825.3:c.537G>T, XM_017021825.2:c.537G>T, XM_017021825.1:c.537G>T, XM_017021831.3:c.537G>T, XM_017021831.2:c.537G>T, XM_017021831.1:c.537G>T, XM_024449761.2:c.537G>T, XM_024449761.1:c.537G>T, XM_024449759.2:c.537G>T, XM_024449759.1:c.537G>T, XM_024449764.2:c.330G>T, XM_024449764.1:c.330G>T, XM_024449776.2:c.537G>T, XM_024449776.1:c.537G>T, XM_024449760.2:c.537G>T, XM_024449760.1:c.537G>T, XM_024449763.2:c.330G>T, XM_024449763.1:c.330G>T, XM_011537397.2:c.120G>T, XM_011537397.1:c.120G>T, XM_047431985.1:c.357G>T, XM_047431990.1:c.537G>T, XM_047431987.1:c.537G>T, NP_004287.3:p.Lys179Asn, NP_001191345.1:p.Lys179Asn, NP_001191348.1:p.Lys179Asn, NP_001191349.1:p.Lys179Asn, NP_001191346.1:p.Lys179Asn, NP_001191347.1:p.Lys179Asn, NP_001191350.1:p.Lys179Asn, NP_001191351.1:p.Lys179Asn, NP_001191353.1:p.Lys179Asn, NP_001191352.1:p.Lys144Asn, NP_001357211.1:p.Lys179Asn, NP_001357206.1:p.Lys179Asn, NP_001357202.1:p.Lys179Asn, NP_001357209.1:p.Lys179Asn, NP_001357220.1:p.Lys179Asn, NP_001357216.1:p.Lys179Asn, NP_001357204.1:p.Lys179Asn, NP_001357215.1:p.Lys179Asn, NP_001357221.1:p.Lys179Asn, NP_001357200.1:p.Lys179Asn, NP_001357213.1:p.Lys179Asn, NP_001357207.1:p.Lys179Asn, NP_001357223.1:p.Lys179Asn, NP_001357217.1:p.Lys179Asn, NP_001357203.1:p.Lys179Asn, NP_001357208.1:p.Lys179Asn, NP_001357199.1:p.Lys179Asn, NP_001357219.1:p.Lys179Asn, NP_001357222.1:p.Lys179Asn, NP_001357201.1:p.Lys179Asn, NP_001357212.1:p.Lys179Asn, NP_001357205.1:p.Lys179Asn, NP_001357218.1:p.Lys179Asn, NP_001357210.1:p.Lys179Asn, XP_016877322.1:p.Lys179Asn, XP_016877309.1:p.Lys179Asn, XP_016877315.1:p.Lys179Asn, XP_016877319.1:p.Lys179Asn, XP_016877321.1:p.Lys179Asn, XP_016877311.1:p.Lys179Asn, XP_016877316.1:p.Lys179Asn, XP_016877317.1:p.Lys179Asn, XP_016877314.1:p.Lys179Asn, XP_016877320.1:p.Lys179Asn, XP_024305529.1:p.Lys179Asn, XP_024305527.1:p.Lys179Asn, XP_024305532.1:p.Lys110Asn, XP_024305544.1:p.Lys179Asn, XP_024305528.1:p.Lys179Asn, XP_024305531.1:p.Lys110Asn, XP_011535699.1:p.Lys40Asn, XP_047287941.1:p.Lys119Asn, XP_047287946.1:p.Lys179Asn, XP_047287943.1:p.Lys179Asn

                    10.

                    rs1470136872 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      T>C,G [Show Flanks]
                      Chromosome:
                      14:72476789 (GRCh38)
                      14:72943497 (GRCh37)
                      Canonical SPDI:
                      NC_000014.9:72476788:T:C,NC_000014.9:72476788:T:G
                      Gene:
                      RGS6 (Varview)
                      Functional Consequence:
                      coding_sequence_variant,missense_variant,synonymous_variant,non_coding_transcript_variant,intron_variant
                      Validated:
                      by frequency,by alfa
                      MAF:
                      C=0./0 (ALFA)
                      G=0.000008/2 (GnomAD_exomes)
                      HGVS:
                      NC_000014.9:g.72476789T>C, NC_000014.9:g.72476789T>G, NC_000014.8:g.72943497T>C, NC_000014.8:g.72943497T>G, NG_029236.1:g.549681T>C, NG_029236.1:g.549681T>G, NM_004296.7:c.741T>C, NM_004296.7:c.741T>G, NM_004296.6:c.741T>C, NM_004296.6:c.741T>G, NM_004296.5:c.741T>C, NM_004296.5:c.741T>G, NM_001204416.3:c.741T>C, NM_001204416.3:c.741T>G, NM_001204416.2:c.741T>C, NM_001204416.2:c.741T>G, NM_001204416.1:c.741T>C, NM_001204416.1:c.741T>G, NM_001204419.3:c.741T>C, NM_001204419.3:c.741T>G, NM_001204419.2:c.741T>C, NM_001204419.2:c.741T>G, NM_001204419.1:c.741T>C, NM_001204419.1:c.741T>G, NM_001204420.3:c.741T>C, NM_001204420.3:c.741T>G, NM_001204420.2:c.741T>C, NM_001204420.2:c.741T>G, NM_001204420.1:c.741T>C, NM_001204420.1:c.741T>G, NM_001204417.3:c.741T>C, NM_001204417.3:c.741T>G, NM_001204417.2:c.741T>C, NM_001204417.2:c.741T>G, NM_001204417.1:c.741T>C, NM_001204417.1:c.741T>G, NM_001204418.3:c.741T>C, NM_001204418.3:c.741T>G, NM_001204418.2:c.741T>C, NM_001204418.2:c.741T>G, NM_001204418.1:c.741T>C, NM_001204418.1:c.741T>G, NM_001204421.3:c.741T>C, NM_001204421.3:c.741T>G, NM_001204421.2:c.741T>C, NM_001204421.2:c.741T>G, NM_001204421.1:c.741T>C, NM_001204421.1:c.741T>G, NM_001204422.3:c.741T>C, NM_001204422.3:c.741T>G, NM_001204422.2:c.741T>C, NM_001204422.2:c.741T>G, NM_001204422.1:c.741T>C, NM_001204422.1:c.741T>G, NM_001204424.2:c.741T>C, NM_001204424.2:c.741T>G, NM_001204424.1:c.741T>C, NM_001204424.1:c.741T>G, NR_135235.2:n.842T>C, NR_135235.2:n.842T>G, NR_135235.1:n.1026T>C, NR_135235.1:n.1026T>G, NM_001204423.2:c.636T>C, NM_001204423.2:c.636T>G, NM_001204423.1:c.636T>C, NM_001204423.1:c.636T>G, NM_001370282.1:c.741T>C, NM_001370282.1:c.741T>G, NM_001370277.1:c.741T>C, NM_001370277.1:c.741T>G, NM_001370273.1:c.741T>C, NM_001370273.1:c.741T>G, NM_001370280.1:c.741T>C, NM_001370280.1:c.741T>G, NM_001370291.1:c.741T>C, NM_001370291.1:c.741T>G, NM_001370287.1:c.741T>C, NM_001370287.1:c.741T>G, NM_001370275.1:c.741T>C, NM_001370275.1:c.741T>G, NM_001370292.1:c.741T>C, NM_001370292.1:c.741T>G, NM_001370271.1:c.741T>C, NM_001370271.1:c.741T>G, NM_001370284.1:c.741T>C, NM_001370284.1:c.741T>G, NM_001370278.1:c.741T>C, NM_001370278.1:c.741T>G, NM_001370294.1:c.741T>C, NM_001370294.1:c.741T>G, NM_001370288.1:c.741T>C, NM_001370288.1:c.741T>G, NM_001370274.1:c.741T>C, NM_001370274.1:c.741T>G, NM_001370279.1:c.732T>C, NM_001370279.1:c.732T>G, NM_001370270.1:c.741T>C, NM_001370270.1:c.741T>G, NM_001370290.1:c.741T>C, NM_001370290.1:c.741T>G, NM_001370293.1:c.741T>C, NM_001370293.1:c.741T>G, NM_001370272.1:c.741T>C, NM_001370272.1:c.741T>G, NM_001370283.1:c.741T>C, NM_001370283.1:c.741T>G, NM_001370276.1:c.741T>C, NM_001370276.1:c.741T>G, NM_001370289.1:c.741T>C, NM_001370289.1:c.741T>G, NM_001370281.1:c.741T>C, NM_001370281.1:c.741T>G, XM_017021833.3:c.741T>C, XM_017021833.3:c.741T>G, XM_017021833.2:c.741T>C, XM_017021833.2:c.741T>G, XM_017021833.1:c.741T>C, XM_017021833.1:c.741T>G, XM_017021820.3:c.741T>C, XM_017021820.3:c.741T>G, XM_017021820.2:c.741T>C, XM_017021820.2:c.741T>G, XM_017021820.1:c.741T>C, XM_017021820.1:c.741T>G, XM_017021826.3:c.741T>C, XM_017021826.3:c.741T>G, XM_017021826.2:c.741T>C, XM_017021826.2:c.741T>G, XM_017021826.1:c.741T>C, XM_017021826.1:c.741T>G, XM_017021830.3:c.741T>C, XM_017021830.3:c.741T>G, XM_017021830.2:c.741T>C, XM_017021830.2:c.741T>G, XM_017021830.1:c.741T>C, XM_017021830.1:c.741T>G, XM_017021832.3:c.741T>C, XM_017021832.3:c.741T>G, XM_017021832.2:c.741T>C, XM_017021832.2:c.741T>G, XM_017021832.1:c.741T>C, XM_017021832.1:c.741T>G, XM_017021822.3:c.741T>C, XM_017021822.3:c.741T>G, XM_017021822.2:c.741T>C, XM_017021822.2:c.741T>G, XM_017021822.1:c.741T>C, XM_017021822.1:c.741T>G, XM_017021827.3:c.741T>C, XM_017021827.3:c.741T>G, XM_017021827.2:c.741T>C, XM_017021827.2:c.741T>G, XM_017021827.1:c.741T>C, XM_017021827.1:c.741T>G, XM_017021828.3:c.741T>C, XM_017021828.3:c.741T>G, XM_017021828.2:c.741T>C, XM_017021828.2:c.741T>G, XM_017021828.1:c.741T>C, XM_017021828.1:c.741T>G, XM_017021825.3:c.741T>C, XM_017021825.3:c.741T>G, XM_017021825.2:c.741T>C, XM_017021825.2:c.741T>G, XM_017021825.1:c.741T>C, XM_017021825.1:c.741T>G, XM_017021831.3:c.741T>C, XM_017021831.3:c.741T>G, XM_017021831.2:c.741T>C, XM_017021831.2:c.741T>G, XM_017021831.1:c.741T>C, XM_017021831.1:c.741T>G, XM_024449761.2:c.741T>C, XM_024449761.2:c.741T>G, XM_024449761.1:c.741T>C, XM_024449761.1:c.741T>G, XM_024449759.2:c.741T>C, XM_024449759.2:c.741T>G, XM_024449759.1:c.741T>C, XM_024449759.1:c.741T>G, XM_024449764.2:c.534T>C, XM_024449764.2:c.534T>G, XM_024449764.1:c.534T>C, XM_024449764.1:c.534T>G, XM_024449776.2:c.741T>C, XM_024449776.2:c.741T>G, XM_024449776.1:c.741T>C, XM_024449776.1:c.741T>G, XM_024449760.2:c.741T>C, XM_024449760.2:c.741T>G, XM_024449760.1:c.741T>C, XM_024449760.1:c.741T>G, XM_024449763.2:c.534T>C, XM_024449763.2:c.534T>G, XM_024449763.1:c.534T>C, XM_024449763.1:c.534T>G, XM_011537397.2:c.324T>C, XM_011537397.2:c.324T>G, XM_011537397.1:c.324T>C, XM_011537397.1:c.324T>G, XM_047431985.1:c.561T>C, XM_047431985.1:c.561T>G, XM_047431988.1:c.99T>C, XM_047431988.1:c.99T>G, XM_047431990.1:c.741T>C, XM_047431990.1:c.741T>G, XM_047431987.1:c.741T>C, XM_047431987.1:c.741T>G, NP_004287.3:p.His247Gln, NP_001191345.1:p.His247Gln, NP_001191348.1:p.His247Gln, NP_001191349.1:p.His247Gln, NP_001191346.1:p.His247Gln, NP_001191347.1:p.His247Gln, NP_001191350.1:p.His247Gln, NP_001191351.1:p.His247Gln, NP_001191353.1:p.His247Gln, NP_001191352.1:p.His212Gln, NP_001357211.1:p.His247Gln, NP_001357206.1:p.His247Gln, NP_001357202.1:p.His247Gln, NP_001357209.1:p.His247Gln, NP_001357220.1:p.His247Gln, NP_001357216.1:p.His247Gln, NP_001357204.1:p.His247Gln, NP_001357221.1:p.His247Gln, NP_001357200.1:p.His247Gln, NP_001357213.1:p.His247Gln, NP_001357207.1:p.His247Gln, NP_001357223.1:p.His247Gln, NP_001357217.1:p.His247Gln, NP_001357203.1:p.His247Gln, NP_001357208.1:p.His244Gln, NP_001357199.1:p.His247Gln, NP_001357219.1:p.His247Gln, NP_001357222.1:p.His247Gln, NP_001357201.1:p.His247Gln, NP_001357212.1:p.His247Gln, NP_001357205.1:p.His247Gln, NP_001357218.1:p.His247Gln, NP_001357210.1:p.His247Gln, XP_016877322.1:p.His247Gln, XP_016877309.1:p.His247Gln, XP_016877315.1:p.His247Gln, XP_016877319.1:p.His247Gln, XP_016877321.1:p.His247Gln, XP_016877311.1:p.His247Gln, XP_016877316.1:p.His247Gln, XP_016877317.1:p.His247Gln, XP_016877314.1:p.His247Gln, XP_016877320.1:p.His247Gln, XP_024305529.1:p.His247Gln, XP_024305527.1:p.His247Gln, XP_024305532.1:p.His178Gln, XP_024305544.1:p.His247Gln, XP_024305528.1:p.His247Gln, XP_024305531.1:p.His178Gln, XP_011535699.1:p.His108Gln, XP_047287941.1:p.His187Gln, XP_047287944.1:p.His33Gln, XP_047287946.1:p.His247Gln, XP_047287943.1:p.His247Gln

                      11.

                      rs1469989506 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        G>A [Show Flanks]
                        Chromosome:
                        14:72510224 (GRCh38)
                        14:72976932 (GRCh37)
                        Canonical SPDI:
                        NC_000014.9:72510223:G:A
                        Gene:
                        RGS6 (Varview)
                        Functional Consequence:
                        missense_variant,intron_variant,non_coding_transcript_variant,coding_sequence_variant
                        Validated:
                        by frequency
                        MAF:
                        A=0.000004/1 (GnomAD_exomes)
                        HGVS:
                        NC_000014.9:g.72510224G>A, NC_000014.8:g.72976932G>A, NG_029236.1:g.583116G>A, NM_004296.7:c.1036G>A, NM_004296.6:c.1036G>A, NM_004296.5:c.1036G>A, NM_001204416.3:c.1036G>A, NM_001204416.2:c.1036G>A, NM_001204416.1:c.1036G>A, NM_001204419.3:c.925G>A, NM_001204419.2:c.925G>A, NM_001204419.1:c.925G>A, NM_001204420.3:c.925G>A, NM_001204420.2:c.925G>A, NM_001204420.1:c.925G>A, NM_001204417.3:c.1036G>A, NM_001204417.2:c.1036G>A, NM_001204417.1:c.1036G>A, NM_001204418.3:c.1036G>A, NM_001204418.2:c.1036G>A, NM_001204418.1:c.1036G>A, NM_001204421.3:c.925G>A, NM_001204421.2:c.925G>A, NM_001204421.1:c.925G>A, NM_001204422.3:c.925G>A, NM_001204422.2:c.925G>A, NM_001204422.1:c.925G>A, NM_001204424.2:c.1036G>A, NM_001204424.1:c.1036G>A, NR_135235.2:n.1137G>A, NR_135235.1:n.1321G>A, NM_001204423.2:c.931G>A, NM_001204423.1:c.931G>A, NM_001370282.1:c.1036G>A, NM_001370277.1:c.1036G>A, NM_001370273.1:c.1036G>A, NM_001370291.1:c.1036G>A, NM_001370287.1:c.1036G>A, NM_001370275.1:c.1036G>A, NM_001370286.1:c.826G>A, NM_001370292.1:c.925G>A, NM_001370271.1:c.1036G>A, NM_001370284.1:c.1036G>A, NM_001370278.1:c.1036G>A, NM_001370288.1:c.1036G>A, NM_001370274.1:c.1036G>A, NM_001370279.1:c.1027G>A, NM_001370270.1:c.1036G>A, NM_001370290.1:c.1036G>A, NM_001370293.1:c.925G>A, NM_001370272.1:c.1036G>A, NM_001370283.1:c.925G>A, NM_001370276.1:c.1036G>A, NM_001370289.1:c.1036G>A, NM_001370281.1:c.1036G>A, XM_017021833.3:c.1036G>A, XM_017021833.2:c.1036G>A, XM_017021833.1:c.1036G>A, XM_017021820.3:c.925G>A, XM_017021820.2:c.925G>A, XM_017021820.1:c.925G>A, XM_017021826.3:c.1036G>A, XM_017021826.2:c.1036G>A, XM_017021826.1:c.1036G>A, XM_017021830.3:c.1036G>A, XM_017021830.2:c.1036G>A, XM_017021830.1:c.1036G>A, XM_017021832.3:c.1036G>A, XM_017021832.2:c.1036G>A, XM_017021832.1:c.1036G>A, XM_017021822.3:c.1036G>A, XM_017021822.2:c.1036G>A, XM_017021822.1:c.1036G>A, XM_017021827.3:c.1036G>A, XM_017021827.2:c.1036G>A, XM_017021827.1:c.1036G>A, XM_017021828.3:c.1036G>A, XM_017021828.2:c.1036G>A, XM_017021828.1:c.1036G>A, XM_017021825.3:c.1036G>A, XM_017021825.2:c.1036G>A, XM_017021825.1:c.1036G>A, XM_017021831.3:c.1036G>A, XM_017021831.2:c.1036G>A, XM_017021831.1:c.1036G>A, XM_024449761.2:c.1036G>A, XM_024449761.1:c.1036G>A, XM_024449759.2:c.1036G>A, XM_024449759.1:c.1036G>A, XM_024449764.2:c.829G>A, XM_024449764.1:c.829G>A, XM_024449776.2:c.925G>A, XM_024449776.1:c.925G>A, XM_024449760.2:c.1036G>A, XM_024449760.1:c.1036G>A, XM_024449763.2:c.829G>A, XM_024449763.1:c.829G>A, XM_011537397.2:c.619G>A, XM_011537397.1:c.619G>A, XM_047431985.1:c.856G>A, XM_047431988.1:c.394G>A, XM_047431990.1:c.925G>A, XM_047431987.1:c.1036G>A, NP_004287.3:p.Gly346Arg, NP_001191345.1:p.Gly346Arg, NP_001191348.1:p.Gly309Arg, NP_001191349.1:p.Gly309Arg, NP_001191346.1:p.Gly346Arg, NP_001191347.1:p.Gly346Arg, NP_001191350.1:p.Gly309Arg, NP_001191351.1:p.Gly309Arg, NP_001191353.1:p.Gly346Arg, NP_001191352.1:p.Gly311Arg, NP_001357211.1:p.Gly346Arg, NP_001357206.1:p.Gly346Arg, NP_001357202.1:p.Gly346Arg, NP_001357220.1:p.Gly346Arg, NP_001357216.1:p.Gly346Arg, NP_001357204.1:p.Gly346Arg, NP_001357215.1:p.Gly276Arg, NP_001357221.1:p.Gly309Arg, NP_001357200.1:p.Gly346Arg, NP_001357213.1:p.Gly346Arg, NP_001357207.1:p.Gly346Arg, NP_001357217.1:p.Gly346Arg, NP_001357203.1:p.Gly346Arg, NP_001357208.1:p.Gly343Arg, NP_001357199.1:p.Gly346Arg, NP_001357219.1:p.Gly346Arg, NP_001357222.1:p.Gly309Arg, NP_001357201.1:p.Gly346Arg, NP_001357212.1:p.Gly309Arg, NP_001357205.1:p.Gly346Arg, NP_001357218.1:p.Gly346Arg, NP_001357210.1:p.Gly346Arg, XP_016877322.1:p.Gly346Arg, XP_016877309.1:p.Gly309Arg, XP_016877315.1:p.Gly346Arg, XP_016877319.1:p.Gly346Arg, XP_016877321.1:p.Gly346Arg, XP_016877311.1:p.Gly346Arg, XP_016877316.1:p.Gly346Arg, XP_016877317.1:p.Gly346Arg, XP_016877314.1:p.Gly346Arg, XP_016877320.1:p.Gly346Arg, XP_024305529.1:p.Gly346Arg, XP_024305527.1:p.Gly346Arg, XP_024305532.1:p.Gly277Arg, XP_024305544.1:p.Gly309Arg, XP_024305528.1:p.Gly346Arg, XP_024305531.1:p.Gly277Arg, XP_011535699.1:p.Gly207Arg, XP_047287941.1:p.Gly286Arg, XP_047287944.1:p.Gly132Arg, XP_047287946.1:p.Gly309Arg, XP_047287943.1:p.Gly346Arg

                        12.

                        rs1469739354 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          T>C [Show Flanks]
                          Chromosome:
                          14:72536221 (GRCh38)
                          14:73002929 (GRCh37)
                          Canonical SPDI:
                          NC_000014.9:72536220:T:C
                          Gene:
                          RGS6 (Varview)
                          Functional Consequence:
                          synonymous_variant,non_coding_transcript_variant,coding_sequence_variant,genic_downstream_transcript_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          C=0./0 (ALFA)
                          C=0.000004/1 (TOPMED)
                          C=0.000007/1 (GnomAD)
                          HGVS:
                          NC_000014.9:g.72536221T>C, NC_000014.8:g.73002929T>C, NG_029236.1:g.609113T>C, NM_004296.7:c.1314T>C, NM_004296.6:c.1314T>C, NM_004296.5:c.1314T>C, NM_001204416.3:c.1314T>C, NM_001204416.2:c.1314T>C, NM_001204416.1:c.1314T>C, NM_001204419.3:c.1203T>C, NM_001204419.2:c.1203T>C, NM_001204419.1:c.1203T>C, NM_001204420.3:c.1203T>C, NM_001204420.2:c.1203T>C, NM_001204420.1:c.1203T>C, NM_001204417.3:c.1314T>C, NM_001204417.2:c.1314T>C, NM_001204417.1:c.1314T>C, NM_001204418.3:c.1314T>C, NM_001204418.2:c.1314T>C, NM_001204418.1:c.1314T>C, NM_001204421.3:c.1203T>C, NM_001204421.2:c.1203T>C, NM_001204421.1:c.1203T>C, NM_001204422.3:c.1203T>C, NM_001204422.2:c.1203T>C, NM_001204422.1:c.1203T>C, NM_001204424.2:c.1314T>C, NM_001204424.1:c.1314T>C, NR_135235.2:n.1415T>C, NR_135235.1:n.1599T>C, NM_001204423.2:c.1209T>C, NM_001204423.1:c.1209T>C, NM_001370282.1:c.1314T>C, NM_001370277.1:c.1314T>C, NM_001370273.1:c.1314T>C, NM_001370280.1:c.1188T>C, NM_001370291.1:c.1314T>C, NM_001370287.1:c.1314T>C, NM_001370275.1:c.1314T>C, NM_001370286.1:c.1104T>C, NM_001370292.1:c.1203T>C, NM_001370271.1:c.1314T>C, NM_001370284.1:c.1314T>C, NM_001370278.1:c.1314T>C, NM_001370294.1:c.1077T>C, NM_001370288.1:c.1314T>C, NM_001370274.1:c.1314T>C, NM_001370279.1:c.1305T>C, NM_001370270.1:c.1314T>C, NM_001370290.1:c.1314T>C, NM_001370293.1:c.1203T>C, NM_001370272.1:c.1314T>C, NM_001370283.1:c.1203T>C, NM_001370276.1:c.1314T>C, NM_001370289.1:c.1314T>C, NM_001370281.1:c.1314T>C, XM_017021820.3:c.1203T>C, XM_017021820.2:c.1203T>C, XM_017021820.1:c.1203T>C, XM_017021826.3:c.1314T>C, XM_017021826.2:c.1314T>C, XM_017021826.1:c.1314T>C, XM_017021830.3:c.1314T>C, XM_017021830.2:c.1314T>C, XM_017021830.1:c.1314T>C, XM_017021832.3:c.1314T>C, XM_017021832.2:c.1314T>C, XM_017021832.1:c.1314T>C, XM_017021822.3:c.1314T>C, XM_017021822.2:c.1314T>C, XM_017021822.1:c.1314T>C, XM_017021827.3:c.1314T>C, XM_017021827.2:c.1314T>C, XM_017021827.1:c.1314T>C, XM_017021828.3:c.1314T>C, XM_017021828.2:c.1314T>C, XM_017021828.1:c.1314T>C, XM_017021825.3:c.1314T>C, XM_017021825.2:c.1314T>C, XM_017021825.1:c.1314T>C, XM_024449761.2:c.1314T>C, XM_024449761.1:c.1314T>C, XM_024449759.2:c.1314T>C, XM_024449759.1:c.1314T>C, XM_024449764.2:c.1107T>C, XM_024449764.1:c.1107T>C, XM_024449776.2:c.1203T>C, XM_024449776.1:c.1203T>C, XM_024449760.2:c.1314T>C, XM_024449760.1:c.1314T>C, XM_024449763.2:c.1107T>C, XM_024449763.1:c.1107T>C, XM_011537397.2:c.897T>C, XM_011537397.1:c.897T>C, XM_047431985.1:c.1134T>C, XM_047431988.1:c.672T>C, XM_047431990.1:c.1203T>C, XM_047431987.1:c.1314T>C

                          13.

                          rs1465474688 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            G>A,T [Show Flanks]
                            Chromosome:
                            14:71964842 (GRCh38)
                            14:72431559 (GRCh37)
                            Canonical SPDI:
                            NC_000014.9:71964841:G:A,NC_000014.9:71964841:G:T
                            Gene:
                            RGS6 (Varview)
                            Functional Consequence:
                            coding_sequence_variant,missense_variant,genic_upstream_transcript_variant,synonymous_variant,non_coding_transcript_variant,intron_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            T=0./0 (ALFA)
                            A=0.000004/1 (GnomAD_exomes)
                            T=0.000004/1 (TOPMED)
                            T=0.000014/2 (GnomAD)
                            HGVS:
                            NC_000014.9:g.71964842G>A, NC_000014.9:g.71964842G>T, NC_000014.8:g.72431559G>A, NC_000014.8:g.72431559G>T, NG_029236.1:g.37743G>A, NG_029236.1:g.37743G>T, NM_004296.7:c.51G>A, NM_004296.7:c.51G>T, NM_004296.6:c.51G>A, NM_004296.6:c.51G>T, NM_004296.5:c.51G>A, NM_004296.5:c.51G>T, NM_001204416.3:c.51G>A, NM_001204416.3:c.51G>T, NM_001204416.2:c.51G>A, NM_001204416.2:c.51G>T, NM_001204416.1:c.51G>A, NM_001204416.1:c.51G>T, NM_001204419.3:c.51G>A, NM_001204419.3:c.51G>T, NM_001204419.2:c.51G>A, NM_001204419.2:c.51G>T, NM_001204419.1:c.51G>A, NM_001204419.1:c.51G>T, NM_001204420.3:c.51G>A, NM_001204420.3:c.51G>T, NM_001204420.2:c.51G>A, NM_001204420.2:c.51G>T, NM_001204420.1:c.51G>A, NM_001204420.1:c.51G>T, NM_001204417.3:c.51G>A, NM_001204417.3:c.51G>T, NM_001204417.2:c.51G>A, NM_001204417.2:c.51G>T, NM_001204417.1:c.51G>A, NM_001204417.1:c.51G>T, NM_001204418.3:c.51G>A, NM_001204418.3:c.51G>T, NM_001204418.2:c.51G>A, NM_001204418.2:c.51G>T, NM_001204418.1:c.51G>A, NM_001204418.1:c.51G>T, NM_001204421.3:c.51G>A, NM_001204421.3:c.51G>T, NM_001204421.2:c.51G>A, NM_001204421.2:c.51G>T, NM_001204421.1:c.51G>A, NM_001204421.1:c.51G>T, NM_001204422.3:c.51G>A, NM_001204422.3:c.51G>T, NM_001204422.2:c.51G>A, NM_001204422.2:c.51G>T, NM_001204422.1:c.51G>A, NM_001204422.1:c.51G>T, NM_001204424.2:c.51G>A, NM_001204424.2:c.51G>T, NM_001204424.1:c.51G>A, NM_001204424.1:c.51G>T, NR_135235.2:n.152G>A, NR_135235.2:n.152G>T, NR_135235.1:n.336G>A, NR_135235.1:n.336G>T, NM_001370282.1:c.51G>A, NM_001370282.1:c.51G>T, NM_001370277.1:c.51G>A, NM_001370277.1:c.51G>T, NM_001370273.1:c.51G>A, NM_001370273.1:c.51G>T, NM_001370280.1:c.51G>A, NM_001370280.1:c.51G>T, NM_001370291.1:c.51G>A, NM_001370291.1:c.51G>T, NM_001370287.1:c.51G>A, NM_001370287.1:c.51G>T, NM_001370275.1:c.51G>A, NM_001370275.1:c.51G>T, NM_001370286.1:c.51G>A, NM_001370286.1:c.51G>T, NM_001370292.1:c.51G>A, NM_001370292.1:c.51G>T, NM_001370271.1:c.51G>A, NM_001370271.1:c.51G>T, NM_001370284.1:c.51G>A, NM_001370284.1:c.51G>T, NM_001370278.1:c.51G>A, NM_001370278.1:c.51G>T, NM_001370294.1:c.51G>A, NM_001370294.1:c.51G>T, NM_001370288.1:c.51G>A, NM_001370288.1:c.51G>T, NM_001370274.1:c.51G>A, NM_001370274.1:c.51G>T, NM_001370279.1:c.51G>A, NM_001370279.1:c.51G>T, NM_001370270.1:c.51G>A, NM_001370270.1:c.51G>T, NM_001370290.1:c.51G>A, NM_001370290.1:c.51G>T, NM_001370293.1:c.51G>A, NM_001370293.1:c.51G>T, NM_001370272.1:c.51G>A, NM_001370272.1:c.51G>T, NM_001370283.1:c.51G>A, NM_001370283.1:c.51G>T, NM_001370276.1:c.51G>A, NM_001370276.1:c.51G>T, NM_001370289.1:c.51G>A, NM_001370289.1:c.51G>T, NM_001370281.1:c.51G>A, NM_001370281.1:c.51G>T, XM_017021833.3:c.51G>A, XM_017021833.3:c.51G>T, XM_017021833.2:c.51G>A, XM_017021833.2:c.51G>T, XM_017021833.1:c.51G>A, XM_017021833.1:c.51G>T, XM_017021820.3:c.51G>A, XM_017021820.3:c.51G>T, XM_017021820.2:c.51G>A, XM_017021820.2:c.51G>T, XM_017021820.1:c.51G>A, XM_017021820.1:c.51G>T, XM_017021826.3:c.51G>A, XM_017021826.3:c.51G>T, XM_017021826.2:c.51G>A, XM_017021826.2:c.51G>T, XM_017021826.1:c.51G>A, XM_017021826.1:c.51G>T, XM_017021830.3:c.51G>A, XM_017021830.3:c.51G>T, XM_017021830.2:c.51G>A, XM_017021830.2:c.51G>T, XM_017021830.1:c.51G>A, XM_017021830.1:c.51G>T, XM_017021832.3:c.51G>A, XM_017021832.3:c.51G>T, XM_017021832.2:c.51G>A, XM_017021832.2:c.51G>T, XM_017021832.1:c.51G>A, XM_017021832.1:c.51G>T, XM_017021822.3:c.51G>A, XM_017021822.3:c.51G>T, XM_017021822.2:c.51G>A, XM_017021822.2:c.51G>T, XM_017021822.1:c.51G>A, XM_017021822.1:c.51G>T, XM_017021827.3:c.51G>A, XM_017021827.3:c.51G>T, XM_017021827.2:c.51G>A, XM_017021827.2:c.51G>T, XM_017021827.1:c.51G>A, XM_017021827.1:c.51G>T, XM_017021828.3:c.51G>A, XM_017021828.3:c.51G>T, XM_017021828.2:c.51G>A, XM_017021828.2:c.51G>T, XM_017021828.1:c.51G>A, XM_017021828.1:c.51G>T, XM_017021825.3:c.51G>A, XM_017021825.3:c.51G>T, XM_017021825.2:c.51G>A, XM_017021825.2:c.51G>T, XM_017021825.1:c.51G>A, XM_017021825.1:c.51G>T, XM_017021831.3:c.51G>A, XM_017021831.3:c.51G>T, XM_017021831.2:c.51G>A, XM_017021831.2:c.51G>T, XM_017021831.1:c.51G>A, XM_017021831.1:c.51G>T, XM_024449761.2:c.51G>A, XM_024449761.2:c.51G>T, XM_024449761.1:c.51G>A, XM_024449761.1:c.51G>T, XM_024449759.2:c.51G>A, XM_024449759.2:c.51G>T, XM_024449759.1:c.51G>A, XM_024449759.1:c.51G>T, XM_024449776.2:c.51G>A, XM_024449776.2:c.51G>T, XM_024449776.1:c.51G>A, XM_024449776.1:c.51G>T, XM_024449760.2:c.51G>A, XM_024449760.2:c.51G>T, XM_024449760.1:c.51G>A, XM_024449760.1:c.51G>T, XM_047431990.1:c.51G>A, XM_047431990.1:c.51G>T, XM_047431987.1:c.51G>A, XM_047431987.1:c.51G>T, NP_004287.3:p.Glu17Asp, NP_001191345.1:p.Glu17Asp, NP_001191348.1:p.Glu17Asp, NP_001191349.1:p.Glu17Asp, NP_001191346.1:p.Glu17Asp, NP_001191347.1:p.Glu17Asp, NP_001191350.1:p.Glu17Asp, NP_001191351.1:p.Glu17Asp, NP_001191353.1:p.Glu17Asp, NP_001357211.1:p.Glu17Asp, NP_001357206.1:p.Glu17Asp, NP_001357202.1:p.Glu17Asp, NP_001357209.1:p.Glu17Asp, NP_001357220.1:p.Glu17Asp, NP_001357216.1:p.Glu17Asp, NP_001357204.1:p.Glu17Asp, NP_001357215.1:p.Glu17Asp, NP_001357221.1:p.Glu17Asp, NP_001357200.1:p.Glu17Asp, NP_001357213.1:p.Glu17Asp, NP_001357207.1:p.Glu17Asp, NP_001357223.1:p.Glu17Asp, NP_001357217.1:p.Glu17Asp, NP_001357203.1:p.Glu17Asp, NP_001357208.1:p.Glu17Asp, NP_001357199.1:p.Glu17Asp, NP_001357219.1:p.Glu17Asp, NP_001357222.1:p.Glu17Asp, NP_001357201.1:p.Glu17Asp, NP_001357212.1:p.Glu17Asp, NP_001357205.1:p.Glu17Asp, NP_001357218.1:p.Glu17Asp, NP_001357210.1:p.Glu17Asp, XP_016877322.1:p.Glu17Asp, XP_016877309.1:p.Glu17Asp, XP_016877315.1:p.Glu17Asp, XP_016877319.1:p.Glu17Asp, XP_016877321.1:p.Glu17Asp, XP_016877311.1:p.Glu17Asp, XP_016877316.1:p.Glu17Asp, XP_016877317.1:p.Glu17Asp, XP_016877314.1:p.Glu17Asp, XP_016877320.1:p.Glu17Asp, XP_024305529.1:p.Glu17Asp, XP_024305527.1:p.Glu17Asp, XP_024305544.1:p.Glu17Asp, XP_024305528.1:p.Glu17Asp, XP_047287946.1:p.Glu17Asp, XP_047287943.1:p.Glu17Asp

                            14.

                            rs1459206177 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              G>C [Show Flanks]
                              Chromosome:
                              14:72518511 (GRCh38)
                              14:72985219 (GRCh37)
                              Canonical SPDI:
                              NC_000014.9:72518510:G:C
                              Gene:
                              RGS6 (Varview)
                              Functional Consequence:
                              coding_sequence_variant,downstream_transcript_variant,missense_variant,non_coding_transcript_variant,genic_downstream_transcript_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              C=0.000045/2 (ALFA)
                              C=0.000014/2 (GnomAD)
                              C=0.000016/4 (GnomAD_exomes)
                              C=0.000019/5 (TOPMED)
                              HGVS:
                              NC_000014.9:g.72518511G>C, NC_000014.8:g.72985219G>C, NG_029236.1:g.591403G>C, NM_004296.7:c.1252G>C, NM_004296.6:c.1252G>C, NM_004296.5:c.1252G>C, NM_001204416.3:c.1252G>C, NM_001204416.2:c.1252G>C, NM_001204416.1:c.1252G>C, NM_001204419.3:c.1141G>C, NM_001204419.2:c.1141G>C, NM_001204419.1:c.1141G>C, NM_001204420.3:c.1141G>C, NM_001204420.2:c.1141G>C, NM_001204420.1:c.1141G>C, NM_001204417.3:c.1252G>C, NM_001204417.2:c.1252G>C, NM_001204417.1:c.1252G>C, NM_001204418.3:c.1252G>C, NM_001204418.2:c.1252G>C, NM_001204418.1:c.1252G>C, NM_001204421.3:c.1141G>C, NM_001204421.2:c.1141G>C, NM_001204421.1:c.1141G>C, NM_001204422.3:c.1141G>C, NM_001204422.2:c.1141G>C, NM_001204422.1:c.1141G>C, NM_001204424.2:c.1252G>C, NM_001204424.1:c.1252G>C, NR_135235.2:n.1353G>C, NR_135235.1:n.1537G>C, NM_001204423.2:c.1147G>C, NM_001204423.1:c.1147G>C, NM_001370282.1:c.1252G>C, NM_001370277.1:c.1252G>C, NM_001370273.1:c.1252G>C, NM_001370280.1:c.1126G>C, NM_001370291.1:c.1252G>C, NM_001370287.1:c.1252G>C, NM_001370275.1:c.1252G>C, NM_001370286.1:c.1042G>C, NM_001370292.1:c.1141G>C, NM_001370271.1:c.1252G>C, NM_001370284.1:c.1252G>C, NM_001370278.1:c.1252G>C, NM_001370294.1:c.1015G>C, NM_001370288.1:c.1252G>C, NM_001370274.1:c.1252G>C, NM_001370279.1:c.1243G>C, NM_001370270.1:c.1252G>C, NM_001370290.1:c.1252G>C, NM_001370293.1:c.1141G>C, NM_001370272.1:c.1252G>C, NM_001370283.1:c.1141G>C, NM_001370276.1:c.1252G>C, NM_001370289.1:c.1252G>C, NM_001370281.1:c.1252G>C, XM_017021820.3:c.1141G>C, XM_017021820.2:c.1141G>C, XM_017021820.1:c.1141G>C, XM_017021826.3:c.1252G>C, XM_017021826.2:c.1252G>C, XM_017021826.1:c.1252G>C, XM_017021830.3:c.1252G>C, XM_017021830.2:c.1252G>C, XM_017021830.1:c.1252G>C, XM_017021832.3:c.1252G>C, XM_017021832.2:c.1252G>C, XM_017021832.1:c.1252G>C, XM_017021822.3:c.1252G>C, XM_017021822.2:c.1252G>C, XM_017021822.1:c.1252G>C, XM_017021827.3:c.1252G>C, XM_017021827.2:c.1252G>C, XM_017021827.1:c.1252G>C, XM_017021828.3:c.1252G>C, XM_017021828.2:c.1252G>C, XM_017021828.1:c.1252G>C, XM_017021825.3:c.1252G>C, XM_017021825.2:c.1252G>C, XM_017021825.1:c.1252G>C, XM_017021831.3:c.1252G>C, XM_017021831.2:c.1252G>C, XM_017021831.1:c.1252G>C, XM_024449761.2:c.1252G>C, XM_024449761.1:c.1252G>C, XM_024449759.2:c.1252G>C, XM_024449759.1:c.1252G>C, XM_024449764.2:c.1045G>C, XM_024449764.1:c.1045G>C, XM_024449776.2:c.1141G>C, XM_024449776.1:c.1141G>C, XM_024449760.2:c.1252G>C, XM_024449760.1:c.1252G>C, XM_024449763.2:c.1045G>C, XM_024449763.1:c.1045G>C, XM_011537397.2:c.835G>C, XM_011537397.1:c.835G>C, XM_047431985.1:c.1072G>C, XM_047431988.1:c.610G>C, XM_047431990.1:c.1141G>C, XM_047431987.1:c.1252G>C, NP_004287.3:p.Gly418Arg, NP_001191345.1:p.Gly418Arg, NP_001191348.1:p.Gly381Arg, NP_001191349.1:p.Gly381Arg, NP_001191346.1:p.Gly418Arg, NP_001191347.1:p.Gly418Arg, NP_001191350.1:p.Gly381Arg, NP_001191351.1:p.Gly381Arg, NP_001191353.1:p.Gly418Arg, NP_001191352.1:p.Gly383Arg, NP_001357211.1:p.Gly418Arg, NP_001357206.1:p.Gly418Arg, NP_001357202.1:p.Gly418Arg, NP_001357209.1:p.Gly376Arg, NP_001357220.1:p.Gly418Arg, NP_001357216.1:p.Gly418Arg, NP_001357204.1:p.Gly418Arg, NP_001357215.1:p.Gly348Arg, NP_001357221.1:p.Gly381Arg, NP_001357200.1:p.Gly418Arg, NP_001357213.1:p.Gly418Arg, NP_001357207.1:p.Gly418Arg, NP_001357223.1:p.Gly339Arg, NP_001357217.1:p.Gly418Arg, NP_001357203.1:p.Gly418Arg, NP_001357208.1:p.Gly415Arg, NP_001357199.1:p.Gly418Arg, NP_001357219.1:p.Gly418Arg, NP_001357222.1:p.Gly381Arg, NP_001357201.1:p.Gly418Arg, NP_001357212.1:p.Gly381Arg, NP_001357205.1:p.Gly418Arg, NP_001357218.1:p.Gly418Arg, NP_001357210.1:p.Gly418Arg, XP_016877309.1:p.Gly381Arg, XP_016877315.1:p.Gly418Arg, XP_016877319.1:p.Gly418Arg, XP_016877321.1:p.Gly418Arg, XP_016877311.1:p.Gly418Arg, XP_016877316.1:p.Gly418Arg, XP_016877317.1:p.Gly418Arg, XP_016877314.1:p.Gly418Arg, XP_016877320.1:p.Gly418Arg, XP_024305529.1:p.Gly418Arg, XP_024305527.1:p.Gly418Arg, XP_024305532.1:p.Gly349Arg, XP_024305544.1:p.Gly381Arg, XP_024305528.1:p.Gly418Arg, XP_024305531.1:p.Gly349Arg, XP_011535699.1:p.Gly279Arg, XP_047287941.1:p.Gly358Arg, XP_047287944.1:p.Gly204Arg, XP_047287946.1:p.Gly381Arg, XP_047287943.1:p.Gly418Arg

                              15.

                              rs1458878108 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                A>G [Show Flanks]
                                Chromosome:
                                14:72472877 (GRCh38)
                                14:72939585 (GRCh37)
                                Canonical SPDI:
                                NC_000014.9:72472876:A:G
                                Gene:
                                RGS6 (Varview)
                                Functional Consequence:
                                coding_sequence_variant,missense_variant,genic_upstream_transcript_variant,non_coding_transcript_variant,upstream_transcript_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                G=0.000224/1 (ALFA)
                                G=0.000007/1 (GnomAD)
                                G=0.000223/1 (Estonian)
                                HGVS:
                                NC_000014.9:g.72472877A>G, NC_000014.8:g.72939585A>G, NG_029236.1:g.545769A>G, NM_004296.7:c.542A>G, NM_004296.6:c.542A>G, NM_004296.5:c.542A>G, NM_001204416.3:c.542A>G, NM_001204416.2:c.542A>G, NM_001204416.1:c.542A>G, NM_001204419.3:c.542A>G, NM_001204419.2:c.542A>G, NM_001204419.1:c.542A>G, NM_001204420.3:c.542A>G, NM_001204420.2:c.542A>G, NM_001204420.1:c.542A>G, NM_001204417.3:c.542A>G, NM_001204417.2:c.542A>G, NM_001204417.1:c.542A>G, NM_001204418.3:c.542A>G, NM_001204418.2:c.542A>G, NM_001204418.1:c.542A>G, NM_001204421.3:c.542A>G, NM_001204421.2:c.542A>G, NM_001204421.1:c.542A>G, NM_001204422.3:c.542A>G, NM_001204422.2:c.542A>G, NM_001204422.1:c.542A>G, NM_001204424.2:c.542A>G, NM_001204424.1:c.542A>G, NR_135235.2:n.643A>G, NR_135235.1:n.827A>G, NM_001204423.2:c.437A>G, NM_001204423.1:c.437A>G, NM_001370282.1:c.542A>G, NM_001370277.1:c.542A>G, NM_001370273.1:c.542A>G, NM_001370280.1:c.542A>G, NM_001370291.1:c.542A>G, NM_001370287.1:c.542A>G, NM_001370275.1:c.542A>G, NM_001370286.1:c.542A>G, NM_001370292.1:c.542A>G, NM_001370271.1:c.542A>G, NM_001370284.1:c.542A>G, NM_001370278.1:c.542A>G, NM_001370294.1:c.542A>G, NM_001370288.1:c.542A>G, NM_001370274.1:c.542A>G, NM_001370279.1:c.542A>G, NM_001370270.1:c.542A>G, NM_001370290.1:c.542A>G, NM_001370293.1:c.542A>G, NM_001370272.1:c.542A>G, NM_001370283.1:c.542A>G, NM_001370276.1:c.542A>G, NM_001370289.1:c.542A>G, NM_001370281.1:c.542A>G, XM_017021833.3:c.542A>G, XM_017021833.2:c.542A>G, XM_017021833.1:c.542A>G, XM_017021820.3:c.542A>G, XM_017021820.2:c.542A>G, XM_017021820.1:c.542A>G, XM_017021826.3:c.542A>G, XM_017021826.2:c.542A>G, XM_017021826.1:c.542A>G, XM_017021830.3:c.542A>G, XM_017021830.2:c.542A>G, XM_017021830.1:c.542A>G, XM_017021832.3:c.542A>G, XM_017021832.2:c.542A>G, XM_017021832.1:c.542A>G, XM_017021822.3:c.542A>G, XM_017021822.2:c.542A>G, XM_017021822.1:c.542A>G, XM_017021827.3:c.542A>G, XM_017021827.2:c.542A>G, XM_017021827.1:c.542A>G, XM_017021828.3:c.542A>G, XM_017021828.2:c.542A>G, XM_017021828.1:c.542A>G, XM_017021825.3:c.542A>G, XM_017021825.2:c.542A>G, XM_017021825.1:c.542A>G, XM_017021831.3:c.542A>G, XM_017021831.2:c.542A>G, XM_017021831.1:c.542A>G, XM_024449761.2:c.542A>G, XM_024449761.1:c.542A>G, XM_024449759.2:c.542A>G, XM_024449759.1:c.542A>G, XM_024449764.2:c.335A>G, XM_024449764.1:c.335A>G, XM_024449776.2:c.542A>G, XM_024449776.1:c.542A>G, XM_024449760.2:c.542A>G, XM_024449760.1:c.542A>G, XM_024449763.2:c.335A>G, XM_024449763.1:c.335A>G, XM_011537397.2:c.125A>G, XM_011537397.1:c.125A>G, XM_047431985.1:c.362A>G, XM_047431990.1:c.542A>G, XM_047431987.1:c.542A>G, NP_004287.3:p.Asp181Gly, NP_001191345.1:p.Asp181Gly, NP_001191348.1:p.Asp181Gly, NP_001191349.1:p.Asp181Gly, NP_001191346.1:p.Asp181Gly, NP_001191347.1:p.Asp181Gly, NP_001191350.1:p.Asp181Gly, NP_001191351.1:p.Asp181Gly, NP_001191353.1:p.Asp181Gly, NP_001191352.1:p.Asp146Gly, NP_001357211.1:p.Asp181Gly, NP_001357206.1:p.Asp181Gly, NP_001357202.1:p.Asp181Gly, NP_001357209.1:p.Asp181Gly, NP_001357220.1:p.Asp181Gly, NP_001357216.1:p.Asp181Gly, NP_001357204.1:p.Asp181Gly, NP_001357215.1:p.Asp181Gly, NP_001357221.1:p.Asp181Gly, NP_001357200.1:p.Asp181Gly, NP_001357213.1:p.Asp181Gly, NP_001357207.1:p.Asp181Gly, NP_001357223.1:p.Asp181Gly, NP_001357217.1:p.Asp181Gly, NP_001357203.1:p.Asp181Gly, NP_001357208.1:p.Asp181Gly, NP_001357199.1:p.Asp181Gly, NP_001357219.1:p.Asp181Gly, NP_001357222.1:p.Asp181Gly, NP_001357201.1:p.Asp181Gly, NP_001357212.1:p.Asp181Gly, NP_001357205.1:p.Asp181Gly, NP_001357218.1:p.Asp181Gly, NP_001357210.1:p.Asp181Gly, XP_016877322.1:p.Asp181Gly, XP_016877309.1:p.Asp181Gly, XP_016877315.1:p.Asp181Gly, XP_016877319.1:p.Asp181Gly, XP_016877321.1:p.Asp181Gly, XP_016877311.1:p.Asp181Gly, XP_016877316.1:p.Asp181Gly, XP_016877317.1:p.Asp181Gly, XP_016877314.1:p.Asp181Gly, XP_016877320.1:p.Asp181Gly, XP_024305529.1:p.Asp181Gly, XP_024305527.1:p.Asp181Gly, XP_024305532.1:p.Asp112Gly, XP_024305544.1:p.Asp181Gly, XP_024305528.1:p.Asp181Gly, XP_024305531.1:p.Asp112Gly, XP_011535699.1:p.Asp42Gly, XP_047287941.1:p.Asp121Gly, XP_047287946.1:p.Asp181Gly, XP_047287943.1:p.Asp181Gly

                                16.

                                rs1457481325 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  A>G [Show Flanks]
                                  Chromosome:
                                  14:72465791 (GRCh38)
                                  14:72932499 (GRCh37)
                                  Canonical SPDI:
                                  NC_000014.9:72465790:A:G
                                  Gene:
                                  RGS6 (Varview)
                                  Functional Consequence:
                                  missense_variant,non_coding_transcript_variant,genic_upstream_transcript_variant,coding_sequence_variant
                                  Validated:
                                  by frequency,by alfa
                                  MAF:
                                  G=0.000084/1 (ALFA)
                                  G=0.000004/1 (TOPMED)
                                  HGVS:
                                  NC_000014.9:g.72465791A>G, NC_000014.8:g.72932499A>G, NG_029236.1:g.538683A>G, NM_004296.7:c.428A>G, NM_004296.6:c.428A>G, NM_004296.5:c.428A>G, NM_001204416.3:c.428A>G, NM_001204416.2:c.428A>G, NM_001204416.1:c.428A>G, NM_001204419.3:c.428A>G, NM_001204419.2:c.428A>G, NM_001204419.1:c.428A>G, NM_001204420.3:c.428A>G, NM_001204420.2:c.428A>G, NM_001204420.1:c.428A>G, NM_001204417.3:c.428A>G, NM_001204417.2:c.428A>G, NM_001204417.1:c.428A>G, NM_001204418.3:c.428A>G, NM_001204418.2:c.428A>G, NM_001204418.1:c.428A>G, NM_001204421.3:c.428A>G, NM_001204421.2:c.428A>G, NM_001204421.1:c.428A>G, NM_001204422.3:c.428A>G, NM_001204422.2:c.428A>G, NM_001204422.1:c.428A>G, NM_001204424.2:c.428A>G, NM_001204424.1:c.428A>G, NR_135235.2:n.529A>G, NR_135235.1:n.713A>G, NM_001204423.2:c.323A>G, NM_001204423.1:c.323A>G, NM_001370282.1:c.428A>G, NM_001370277.1:c.428A>G, NM_001370273.1:c.428A>G, NM_001370280.1:c.428A>G, NM_001370291.1:c.428A>G, NM_001370287.1:c.428A>G, NM_001370275.1:c.428A>G, NM_001370286.1:c.428A>G, NM_001370292.1:c.428A>G, NM_001370271.1:c.428A>G, NM_001370284.1:c.428A>G, NM_001370278.1:c.428A>G, NM_001370294.1:c.428A>G, NM_001370288.1:c.428A>G, NM_001370274.1:c.428A>G, NM_001370279.1:c.428A>G, NM_001370270.1:c.428A>G, NM_001370290.1:c.428A>G, NM_001370293.1:c.428A>G, NM_001370272.1:c.428A>G, NM_001370283.1:c.428A>G, NM_001370276.1:c.428A>G, NM_001370289.1:c.428A>G, NM_001370281.1:c.428A>G, XM_017021833.3:c.428A>G, XM_017021833.2:c.428A>G, XM_017021833.1:c.428A>G, XM_017021820.3:c.428A>G, XM_017021820.2:c.428A>G, XM_017021820.1:c.428A>G, XM_017021826.3:c.428A>G, XM_017021826.2:c.428A>G, XM_017021826.1:c.428A>G, XM_017021830.3:c.428A>G, XM_017021830.2:c.428A>G, XM_017021830.1:c.428A>G, XM_017021832.3:c.428A>G, XM_017021832.2:c.428A>G, XM_017021832.1:c.428A>G, XM_017021822.3:c.428A>G, XM_017021822.2:c.428A>G, XM_017021822.1:c.428A>G, XM_017021827.3:c.428A>G, XM_017021827.2:c.428A>G, XM_017021827.1:c.428A>G, XM_017021828.3:c.428A>G, XM_017021828.2:c.428A>G, XM_017021828.1:c.428A>G, XM_017021825.3:c.428A>G, XM_017021825.2:c.428A>G, XM_017021825.1:c.428A>G, XM_017021831.3:c.428A>G, XM_017021831.2:c.428A>G, XM_017021831.1:c.428A>G, XM_024449761.2:c.428A>G, XM_024449761.1:c.428A>G, XM_024449759.2:c.428A>G, XM_024449759.1:c.428A>G, XM_024449764.2:c.221A>G, XM_024449764.1:c.221A>G, XM_024449776.2:c.428A>G, XM_024449776.1:c.428A>G, XM_024449760.2:c.428A>G, XM_024449760.1:c.428A>G, XM_024449763.2:c.221A>G, XM_024449763.1:c.221A>G, XM_011537397.2:c.11A>G, XM_011537397.1:c.11A>G, XM_047431985.1:c.248A>G, XM_047431990.1:c.428A>G, XM_047431987.1:c.428A>G, NP_004287.3:p.Lys143Arg, NP_001191345.1:p.Lys143Arg, NP_001191348.1:p.Lys143Arg, NP_001191349.1:p.Lys143Arg, NP_001191346.1:p.Lys143Arg, NP_001191347.1:p.Lys143Arg, NP_001191350.1:p.Lys143Arg, NP_001191351.1:p.Lys143Arg, NP_001191353.1:p.Lys143Arg, NP_001191352.1:p.Lys108Arg, NP_001357211.1:p.Lys143Arg, NP_001357206.1:p.Lys143Arg, NP_001357202.1:p.Lys143Arg, NP_001357209.1:p.Lys143Arg, NP_001357220.1:p.Lys143Arg, NP_001357216.1:p.Lys143Arg, NP_001357204.1:p.Lys143Arg, NP_001357215.1:p.Lys143Arg, NP_001357221.1:p.Lys143Arg, NP_001357200.1:p.Lys143Arg, NP_001357213.1:p.Lys143Arg, NP_001357207.1:p.Lys143Arg, NP_001357223.1:p.Lys143Arg, NP_001357217.1:p.Lys143Arg, NP_001357203.1:p.Lys143Arg, NP_001357208.1:p.Lys143Arg, NP_001357199.1:p.Lys143Arg, NP_001357219.1:p.Lys143Arg, NP_001357222.1:p.Lys143Arg, NP_001357201.1:p.Lys143Arg, NP_001357212.1:p.Lys143Arg, NP_001357205.1:p.Lys143Arg, NP_001357218.1:p.Lys143Arg, NP_001357210.1:p.Lys143Arg, XP_016877322.1:p.Lys143Arg, XP_016877309.1:p.Lys143Arg, XP_016877315.1:p.Lys143Arg, XP_016877319.1:p.Lys143Arg, XP_016877321.1:p.Lys143Arg, XP_016877311.1:p.Lys143Arg, XP_016877316.1:p.Lys143Arg, XP_016877317.1:p.Lys143Arg, XP_016877314.1:p.Lys143Arg, XP_016877320.1:p.Lys143Arg, XP_024305529.1:p.Lys143Arg, XP_024305527.1:p.Lys143Arg, XP_024305532.1:p.Lys74Arg, XP_024305544.1:p.Lys143Arg, XP_024305528.1:p.Lys143Arg, XP_024305531.1:p.Lys74Arg, XP_011535699.1:p.Lys4Arg, XP_047287941.1:p.Lys83Arg, XP_047287946.1:p.Lys143Arg, XP_047287943.1:p.Lys143Arg

                                  17.

                                  rs1456543062 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    C>T [Show Flanks]
                                    Chromosome:
                                    14:72352187 (GRCh38)
                                    14:72818895 (GRCh37)
                                    Canonical SPDI:
                                    NC_000014.9:72352186:C:T
                                    Gene:
                                    RGS6 (Varview)
                                    Functional Consequence:
                                    synonymous_variant,non_coding_transcript_variant,genic_upstream_transcript_variant,coding_sequence_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    T=0./0 (ALFA)
                                    T=0.000007/1 (GnomAD)
                                    T=0.000011/3 (TOPMED)
                                    HGVS:
                                    NC_000014.9:g.72352187C>T, NC_000014.8:g.72818895C>T, NG_029236.1:g.425079C>T, NM_004296.7:c.177C>T, NM_004296.6:c.177C>T, NM_004296.5:c.177C>T, NM_001204416.3:c.177C>T, NM_001204416.2:c.177C>T, NM_001204416.1:c.177C>T, NM_001204419.3:c.177C>T, NM_001204419.2:c.177C>T, NM_001204419.1:c.177C>T, NM_001204420.3:c.177C>T, NM_001204420.2:c.177C>T, NM_001204420.1:c.177C>T, NM_001204417.3:c.177C>T, NM_001204417.2:c.177C>T, NM_001204417.1:c.177C>T, NM_001204418.3:c.177C>T, NM_001204418.2:c.177C>T, NM_001204418.1:c.177C>T, NM_001204421.3:c.177C>T, NM_001204421.2:c.177C>T, NM_001204421.1:c.177C>T, NM_001204422.3:c.177C>T, NM_001204422.2:c.177C>T, NM_001204422.1:c.177C>T, NM_001204424.2:c.177C>T, NM_001204424.1:c.177C>T, NR_135235.2:n.278C>T, NR_135235.1:n.462C>T, NM_001204423.2:c.72C>T, NM_001204423.1:c.72C>T, NM_001370282.1:c.177C>T, NM_001370277.1:c.177C>T, NM_001370273.1:c.177C>T, NM_001370280.1:c.177C>T, NM_001370291.1:c.177C>T, NM_001370287.1:c.177C>T, NM_001370275.1:c.177C>T, NM_001370286.1:c.177C>T, NM_001370292.1:c.177C>T, NM_001370271.1:c.177C>T, NM_001370284.1:c.177C>T, NM_001370278.1:c.177C>T, NM_001370294.1:c.177C>T, NM_001370288.1:c.177C>T, NM_001370274.1:c.177C>T, NM_001370279.1:c.177C>T, NM_001370270.1:c.177C>T, NM_001370290.1:c.177C>T, NM_001370293.1:c.177C>T, NM_001370272.1:c.177C>T, NM_001370283.1:c.177C>T, NM_001370276.1:c.177C>T, NM_001370289.1:c.177C>T, NM_001370281.1:c.177C>T, XM_017021833.3:c.177C>T, XM_017021833.2:c.177C>T, XM_017021833.1:c.177C>T, XM_017021820.3:c.177C>T, XM_017021820.2:c.177C>T, XM_017021820.1:c.177C>T, XM_017021826.3:c.177C>T, XM_017021826.2:c.177C>T, XM_017021826.1:c.177C>T, XM_017021830.3:c.177C>T, XM_017021830.2:c.177C>T, XM_017021830.1:c.177C>T, XM_017021832.3:c.177C>T, XM_017021832.2:c.177C>T, XM_017021832.1:c.177C>T, XM_017021822.3:c.177C>T, XM_017021822.2:c.177C>T, XM_017021822.1:c.177C>T, XM_017021827.3:c.177C>T, XM_017021827.2:c.177C>T, XM_017021827.1:c.177C>T, XM_017021828.3:c.177C>T, XM_017021828.2:c.177C>T, XM_017021828.1:c.177C>T, XM_017021825.3:c.177C>T, XM_017021825.2:c.177C>T, XM_017021825.1:c.177C>T, XM_017021831.3:c.177C>T, XM_017021831.2:c.177C>T, XM_017021831.1:c.177C>T, XM_024449761.2:c.177C>T, XM_024449761.1:c.177C>T, XM_024449759.2:c.177C>T, XM_024449759.1:c.177C>T, XM_024449776.2:c.177C>T, XM_024449776.1:c.177C>T, XM_024449760.2:c.177C>T, XM_024449760.1:c.177C>T, XM_047431990.1:c.177C>T, XM_047431987.1:c.177C>T

                                    18.

                                    rs1456275163 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      T>C [Show Flanks]
                                      Chromosome:
                                      14:71964867 (GRCh38)
                                      14:72431584 (GRCh37)
                                      Canonical SPDI:
                                      NC_000014.9:71964866:T:C
                                      Gene:
                                      RGS6 (Varview)
                                      Functional Consequence:
                                      coding_sequence_variant,missense_variant,genic_upstream_transcript_variant,non_coding_transcript_variant,intron_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      C=0.000045/2 (ALFA)
                                      C=0.000004/1 (TOPMED)
                                      C=0.000007/1 (GnomAD)
                                      C=0.000008/2 (GnomAD_exomes)
                                      HGVS:
                                      NC_000014.9:g.71964867T>C, NC_000014.8:g.72431584T>C, NG_029236.1:g.37768T>C, NM_004296.7:c.76T>C, NM_004296.6:c.76T>C, NM_004296.5:c.76T>C, NM_001204416.3:c.76T>C, NM_001204416.2:c.76T>C, NM_001204416.1:c.76T>C, NM_001204419.3:c.76T>C, NM_001204419.2:c.76T>C, NM_001204419.1:c.76T>C, NM_001204420.3:c.76T>C, NM_001204420.2:c.76T>C, NM_001204420.1:c.76T>C, NM_001204417.3:c.76T>C, NM_001204417.2:c.76T>C, NM_001204417.1:c.76T>C, NM_001204418.3:c.76T>C, NM_001204418.2:c.76T>C, NM_001204418.1:c.76T>C, NM_001204421.3:c.76T>C, NM_001204421.2:c.76T>C, NM_001204421.1:c.76T>C, NM_001204422.3:c.76T>C, NM_001204422.2:c.76T>C, NM_001204422.1:c.76T>C, NM_001204424.2:c.76T>C, NM_001204424.1:c.76T>C, NR_135235.2:n.177T>C, NR_135235.1:n.361T>C, NM_001370282.1:c.76T>C, NM_001370277.1:c.76T>C, NM_001370273.1:c.76T>C, NM_001370280.1:c.76T>C, NM_001370291.1:c.76T>C, NM_001370287.1:c.76T>C, NM_001370275.1:c.76T>C, NM_001370286.1:c.76T>C, NM_001370292.1:c.76T>C, NM_001370271.1:c.76T>C, NM_001370284.1:c.76T>C, NM_001370278.1:c.76T>C, NM_001370294.1:c.76T>C, NM_001370288.1:c.76T>C, NM_001370274.1:c.76T>C, NM_001370279.1:c.76T>C, NM_001370270.1:c.76T>C, NM_001370290.1:c.76T>C, NM_001370293.1:c.76T>C, NM_001370272.1:c.76T>C, NM_001370283.1:c.76T>C, NM_001370276.1:c.76T>C, NM_001370289.1:c.76T>C, NM_001370281.1:c.76T>C, XM_017021833.3:c.76T>C, XM_017021833.2:c.76T>C, XM_017021833.1:c.76T>C, XM_017021820.3:c.76T>C, XM_017021820.2:c.76T>C, XM_017021820.1:c.76T>C, XM_017021826.3:c.76T>C, XM_017021826.2:c.76T>C, XM_017021826.1:c.76T>C, XM_017021830.3:c.76T>C, XM_017021830.2:c.76T>C, XM_017021830.1:c.76T>C, XM_017021832.3:c.76T>C, XM_017021832.2:c.76T>C, XM_017021832.1:c.76T>C, XM_017021822.3:c.76T>C, XM_017021822.2:c.76T>C, XM_017021822.1:c.76T>C, XM_017021827.3:c.76T>C, XM_017021827.2:c.76T>C, XM_017021827.1:c.76T>C, XM_017021828.3:c.76T>C, XM_017021828.2:c.76T>C, XM_017021828.1:c.76T>C, XM_017021825.3:c.76T>C, XM_017021825.2:c.76T>C, XM_017021825.1:c.76T>C, XM_017021831.3:c.76T>C, XM_017021831.2:c.76T>C, XM_017021831.1:c.76T>C, XM_024449761.2:c.76T>C, XM_024449761.1:c.76T>C, XM_024449759.2:c.76T>C, XM_024449759.1:c.76T>C, XM_024449776.2:c.76T>C, XM_024449776.1:c.76T>C, XM_024449760.2:c.76T>C, XM_024449760.1:c.76T>C, XM_047431990.1:c.76T>C, XM_047431987.1:c.76T>C, NP_004287.3:p.Tyr26His, NP_001191345.1:p.Tyr26His, NP_001191348.1:p.Tyr26His, NP_001191349.1:p.Tyr26His, NP_001191346.1:p.Tyr26His, NP_001191347.1:p.Tyr26His, NP_001191350.1:p.Tyr26His, NP_001191351.1:p.Tyr26His, NP_001191353.1:p.Tyr26His, NP_001357211.1:p.Tyr26His, NP_001357206.1:p.Tyr26His, NP_001357202.1:p.Tyr26His, NP_001357209.1:p.Tyr26His, NP_001357220.1:p.Tyr26His, NP_001357216.1:p.Tyr26His, NP_001357204.1:p.Tyr26His, NP_001357215.1:p.Tyr26His, NP_001357221.1:p.Tyr26His, NP_001357200.1:p.Tyr26His, NP_001357213.1:p.Tyr26His, NP_001357207.1:p.Tyr26His, NP_001357223.1:p.Tyr26His, NP_001357217.1:p.Tyr26His, NP_001357203.1:p.Tyr26His, NP_001357208.1:p.Tyr26His, NP_001357199.1:p.Tyr26His, NP_001357219.1:p.Tyr26His, NP_001357222.1:p.Tyr26His, NP_001357201.1:p.Tyr26His, NP_001357212.1:p.Tyr26His, NP_001357205.1:p.Tyr26His, NP_001357218.1:p.Tyr26His, NP_001357210.1:p.Tyr26His, XP_016877322.1:p.Tyr26His, XP_016877309.1:p.Tyr26His, XP_016877315.1:p.Tyr26His, XP_016877319.1:p.Tyr26His, XP_016877321.1:p.Tyr26His, XP_016877311.1:p.Tyr26His, XP_016877316.1:p.Tyr26His, XP_016877317.1:p.Tyr26His, XP_016877314.1:p.Tyr26His, XP_016877320.1:p.Tyr26His, XP_024305529.1:p.Tyr26His, XP_024305527.1:p.Tyr26His, XP_024305544.1:p.Tyr26His, XP_024305528.1:p.Tyr26His, XP_047287946.1:p.Tyr26His, XP_047287943.1:p.Tyr26His

                                      19.

                                      rs1452128412 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        C>A [Show Flanks]
                                        Chromosome:
                                        14:72465809 (GRCh38)
                                        14:72932517 (GRCh37)
                                        Canonical SPDI:
                                        NC_000014.9:72465808:C:A
                                        Gene:
                                        RGS6 (Varview)
                                        Functional Consequence:
                                        genic_upstream_transcript_variant,coding_sequence_variant,missense_variant,non_coding_transcript_variant
                                        Validated:
                                        by frequency,by alfa
                                        MAF:
                                        A=0./0 (ALFA)
                                        HGVS:
                                        NC_000014.9:g.72465809C>A, NC_000014.8:g.72932517C>A, NG_029236.1:g.538701C>A, NM_004296.7:c.446C>A, NM_004296.6:c.446C>A, NM_004296.5:c.446C>A, NM_001204416.3:c.446C>A, NM_001204416.2:c.446C>A, NM_001204416.1:c.446C>A, NM_001204419.3:c.446C>A, NM_001204419.2:c.446C>A, NM_001204419.1:c.446C>A, NM_001204420.3:c.446C>A, NM_001204420.2:c.446C>A, NM_001204420.1:c.446C>A, NM_001204417.3:c.446C>A, NM_001204417.2:c.446C>A, NM_001204417.1:c.446C>A, NM_001204418.3:c.446C>A, NM_001204418.2:c.446C>A, NM_001204418.1:c.446C>A, NM_001204421.3:c.446C>A, NM_001204421.2:c.446C>A, NM_001204421.1:c.446C>A, NM_001204422.3:c.446C>A, NM_001204422.2:c.446C>A, NM_001204422.1:c.446C>A, NM_001204424.2:c.446C>A, NM_001204424.1:c.446C>A, NR_135235.2:n.547C>A, NR_135235.1:n.731C>A, NM_001204423.2:c.341C>A, NM_001204423.1:c.341C>A, NM_001370282.1:c.446C>A, NM_001370277.1:c.446C>A, NM_001370273.1:c.446C>A, NM_001370280.1:c.446C>A, NM_001370291.1:c.446C>A, NM_001370287.1:c.446C>A, NM_001370275.1:c.446C>A, NM_001370286.1:c.446C>A, NM_001370292.1:c.446C>A, NM_001370271.1:c.446C>A, NM_001370284.1:c.446C>A, NM_001370278.1:c.446C>A, NM_001370294.1:c.446C>A, NM_001370288.1:c.446C>A, NM_001370274.1:c.446C>A, NM_001370279.1:c.446C>A, NM_001370270.1:c.446C>A, NM_001370290.1:c.446C>A, NM_001370293.1:c.446C>A, NM_001370272.1:c.446C>A, NM_001370283.1:c.446C>A, NM_001370276.1:c.446C>A, NM_001370289.1:c.446C>A, NM_001370281.1:c.446C>A, XM_017021833.3:c.446C>A, XM_017021833.2:c.446C>A, XM_017021833.1:c.446C>A, XM_017021820.3:c.446C>A, XM_017021820.2:c.446C>A, XM_017021820.1:c.446C>A, XM_017021826.3:c.446C>A, XM_017021826.2:c.446C>A, XM_017021826.1:c.446C>A, XM_017021830.3:c.446C>A, XM_017021830.2:c.446C>A, XM_017021830.1:c.446C>A, XM_017021832.3:c.446C>A, XM_017021832.2:c.446C>A, XM_017021832.1:c.446C>A, XM_017021822.3:c.446C>A, XM_017021822.2:c.446C>A, XM_017021822.1:c.446C>A, XM_017021827.3:c.446C>A, XM_017021827.2:c.446C>A, XM_017021827.1:c.446C>A, XM_017021828.3:c.446C>A, XM_017021828.2:c.446C>A, XM_017021828.1:c.446C>A, XM_017021825.3:c.446C>A, XM_017021825.2:c.446C>A, XM_017021825.1:c.446C>A, XM_017021831.3:c.446C>A, XM_017021831.2:c.446C>A, XM_017021831.1:c.446C>A, XM_024449761.2:c.446C>A, XM_024449761.1:c.446C>A, XM_024449759.2:c.446C>A, XM_024449759.1:c.446C>A, XM_024449764.2:c.239C>A, XM_024449764.1:c.239C>A, XM_024449776.2:c.446C>A, XM_024449776.1:c.446C>A, XM_024449760.2:c.446C>A, XM_024449760.1:c.446C>A, XM_024449763.2:c.239C>A, XM_024449763.1:c.239C>A, XM_011537397.2:c.29C>A, XM_011537397.1:c.29C>A, XM_047431985.1:c.266C>A, XM_047431990.1:c.446C>A, XM_047431987.1:c.446C>A, NP_004287.3:p.Ala149Glu, NP_001191345.1:p.Ala149Glu, NP_001191348.1:p.Ala149Glu, NP_001191349.1:p.Ala149Glu, NP_001191346.1:p.Ala149Glu, NP_001191347.1:p.Ala149Glu, NP_001191350.1:p.Ala149Glu, NP_001191351.1:p.Ala149Glu, NP_001191353.1:p.Ala149Glu, NP_001191352.1:p.Ala114Glu, NP_001357211.1:p.Ala149Glu, NP_001357206.1:p.Ala149Glu, NP_001357202.1:p.Ala149Glu, NP_001357209.1:p.Ala149Glu, NP_001357220.1:p.Ala149Glu, NP_001357216.1:p.Ala149Glu, NP_001357204.1:p.Ala149Glu, NP_001357215.1:p.Ala149Glu, NP_001357221.1:p.Ala149Glu, NP_001357200.1:p.Ala149Glu, NP_001357213.1:p.Ala149Glu, NP_001357207.1:p.Ala149Glu, NP_001357223.1:p.Ala149Glu, NP_001357217.1:p.Ala149Glu, NP_001357203.1:p.Ala149Glu, NP_001357208.1:p.Ala149Glu, NP_001357199.1:p.Ala149Glu, NP_001357219.1:p.Ala149Glu, NP_001357222.1:p.Ala149Glu, NP_001357201.1:p.Ala149Glu, NP_001357212.1:p.Ala149Glu, NP_001357205.1:p.Ala149Glu, NP_001357218.1:p.Ala149Glu, NP_001357210.1:p.Ala149Glu, XP_016877322.1:p.Ala149Glu, XP_016877309.1:p.Ala149Glu, XP_016877315.1:p.Ala149Glu, XP_016877319.1:p.Ala149Glu, XP_016877321.1:p.Ala149Glu, XP_016877311.1:p.Ala149Glu, XP_016877316.1:p.Ala149Glu, XP_016877317.1:p.Ala149Glu, XP_016877314.1:p.Ala149Glu, XP_016877320.1:p.Ala149Glu, XP_024305529.1:p.Ala149Glu, XP_024305527.1:p.Ala149Glu, XP_024305532.1:p.Ala80Glu, XP_024305544.1:p.Ala149Glu, XP_024305528.1:p.Ala149Glu, XP_024305531.1:p.Ala80Glu, XP_011535699.1:p.Ala10Glu, XP_047287941.1:p.Ala89Glu, XP_047287946.1:p.Ala149Glu, XP_047287943.1:p.Ala149Glu

                                        20.

                                        rs1450278260 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          G>A [Show Flanks]
                                          Chromosome:
                                          14:72562743 (GRCh38)
                                          14:73029451 (GRCh37)
                                          Canonical SPDI:
                                          NC_000014.9:72562742:G:A
                                          Gene:
                                          RGS6 (Varview)
                                          Functional Consequence:
                                          genic_downstream_transcript_variant,coding_sequence_variant,non_coding_transcript_variant,3_prime_UTR_variant,intron_variant,missense_variant
                                          Validated:
                                          by frequency
                                          MAF:
                                          A=0.000007/1 (GnomAD_exomes)
                                          HGVS:
                                          NC_000014.9:g.72562743G>A, NC_000014.8:g.73029451G>A, NG_029236.1:g.635635G>A, NM_004296.7:c.*276G>A, NM_004296.6:c.*276G>A, NM_004296.5:c.*276G>A, NM_001204416.3:c.*276G>A, NM_001204416.2:c.*276G>A, NM_001204416.1:c.*276G>A, NM_001204419.3:c.*276G>A, NM_001204419.2:c.*276G>A, NM_001204419.1:c.*276G>A, NM_001204420.3:c.*276G>A, NM_001204420.2:c.*276G>A, NM_001204420.1:c.*276G>A, NM_001204417.3:c.1451G>A, NM_001204417.2:c.1451G>A, NM_001204417.1:c.1451G>A, NM_001204418.3:c.1397G>A, NM_001204418.2:c.1397G>A, NM_001204418.1:c.1397G>A, NM_001204421.3:c.1340G>A, NM_001204421.2:c.1340G>A, NM_001204421.1:c.1340G>A, NM_001204422.3:c.1286G>A, NM_001204422.2:c.1286G>A, NM_001204422.1:c.1286G>A, NM_001204424.2:c.*276G>A, NM_001204424.1:c.*276G>A, NR_135235.2:n.1913G>A, NR_135235.1:n.2097G>A, NM_001204423.2:c.*276G>A, NM_001204423.1:c.*276G>A, NM_001370282.1:c.*341G>A, NM_001370277.1:c.*290G>A, NM_001370273.1:c.*154G>A, NM_001370280.1:c.*154G>A, NM_001370291.1:c.*347G>A, NM_001370287.1:c.*276G>A, NM_001370275.1:c.1687G>A, NM_001370286.1:c.*154G>A, NM_001370292.1:c.*276G>A, NM_001370271.1:c.*154G>A, NM_001370284.1:c.*276G>A, NM_001370278.1:c.*154G>A, NM_001370294.1:c.*276G>A, NM_001370288.1:c.*276G>A, NM_001370274.1:c.*154G>A, NM_001370279.1:c.*154G>A, NM_001370270.1:c.*154G>A, NM_001370290.1:c.*347G>A, NM_001370293.1:c.*276G>A, NM_001370272.1:c.*60G>A, NM_001370283.1:c.*154G>A, NM_001370276.1:c.1687G>A, NM_001370289.1:c.*276G>A, NM_001370281.1:c.*3G>A, XM_017021820.3:c.1660G>A, XM_017021820.2:c.1660G>A, XM_017021820.1:c.1660G>A, XM_024449761.2:c.1771G>A, XM_024449761.1:c.1771G>A, XM_024449759.2:c.1771G>A, XM_024449759.1:c.1771G>A, XM_024449764.2:c.1564G>A, XM_024449764.1:c.1564G>A, XM_024449776.2:c.*276G>A, XM_024449776.1:c.*276G>A, XM_024449760.2:c.1771G>A, XM_024449760.1:c.1771G>A, XM_024449763.2:c.1564G>A, XM_024449763.1:c.1564G>A, XM_011537397.2:c.1354G>A, XM_011537397.1:c.1354G>A, XM_047431985.1:c.1591G>A, XM_047431988.1:c.1129G>A, NP_001191346.1:p.Arg484Lys, NP_001191347.1:p.Arg466Lys, NP_001191350.1:p.Arg447Lys, NP_001191351.1:p.Arg429Lys, NP_001357204.1:p.Gly563Ser, NP_001357205.1:p.Gly563Ser, XP_016877309.1:p.Gly554Ser, XP_024305529.1:p.Gly591Ser, XP_024305527.1:p.Gly591Ser, XP_024305532.1:p.Gly522Ser, XP_024305528.1:p.Gly591Ser, XP_024305531.1:p.Gly522Ser, XP_011535699.1:p.Gly452Ser, XP_047287941.1:p.Gly531Ser, XP_047287944.1:p.Gly377Ser

                                          Display Settings:

                                          Format
                                          Items per page
                                          Sort by

                                          Send to:

                                          Choose Destination

                                          Supplemental Content

                                          Filters: Manage Filters

                                          Find related data

                                          Recent activity

                                          Clear Turn Off Turn On

                                          Your browsing activity is empty.

                                          Activity recording is turned off.

                                          Turn recording back on

                                          See more...