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Links from Protein

Items: 1 to 20 of 720

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rs1485673938 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>A,C [Show Flanks]
    Chromosome:
    10:31908497 (GRCh38)
    10:32197425 (GRCh37)
    Canonical SPDI:
    NC_000010.11:31908496:G:A,NC_000010.11:31908496:G:C
    Gene:
    ARHGAP12 (Varview)
    Functional Consequence:
    coding_sequence_variant,missense_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    A=0.000031/1 (ALFA)
    C=0.000004/1 (GnomAD_exomes)
    A=0.000004/1 (TOPMED)
    HGVS:
    NC_000010.11:g.31908497G>A, NC_000010.11:g.31908497G>C, NC_000010.10:g.32197425G>A, NC_000010.10:g.32197425G>C, NM_018287.7:c.359C>T, NM_018287.7:c.359C>G, NM_018287.6:c.359C>T, NM_018287.6:c.359C>G, XM_005252644.3:c.359C>T, XM_005252644.3:c.359C>G, XM_005252644.2:c.359C>T, XM_005252644.2:c.359C>G, XM_005252644.1:c.359C>T, XM_005252644.1:c.359C>G, XM_011519761.3:c.359C>T, XM_011519761.3:c.359C>G, XM_011519761.2:c.359C>T, XM_011519761.2:c.359C>G, XM_011519761.1:c.359C>T, XM_011519761.1:c.359C>G, XM_017016954.3:c.359C>T, XM_017016954.3:c.359C>G, XM_017016954.2:c.359C>T, XM_017016954.2:c.359C>G, XM_017016954.1:c.359C>T, XM_017016954.1:c.359C>G, NM_001270696.2:c.359C>T, NM_001270696.2:c.359C>G, NM_001270696.1:c.359C>T, NM_001270696.1:c.359C>G, NM_001270698.2:c.359C>T, NM_001270698.2:c.359C>G, NM_001270698.1:c.359C>T, NM_001270698.1:c.359C>G, NM_001270695.1:c.359C>T, NM_001270695.1:c.359C>G, NM_001270697.1:c.359C>T, NM_001270697.1:c.359C>G, XM_047426021.1:c.359C>T, XM_047426021.1:c.359C>G, NM_001270699.1:c.359C>T, NM_001270699.1:c.359C>G, NP_060757.4:p.Ser120Leu, NP_060757.4:p.Ser120Trp, XP_005252701.1:p.Ser120Leu, XP_005252701.1:p.Ser120Trp, XP_011518063.1:p.Ser120Leu, XP_011518063.1:p.Ser120Trp, XP_016872443.1:p.Ser120Leu, XP_016872443.1:p.Ser120Trp, NP_001257625.1:p.Ser120Leu, NP_001257625.1:p.Ser120Trp, NP_001257627.1:p.Ser120Leu, NP_001257627.1:p.Ser120Trp, NP_001257624.1:p.Ser120Leu, NP_001257624.1:p.Ser120Trp, NP_001257626.1:p.Ser120Leu, NP_001257626.1:p.Ser120Trp, XP_047281977.1:p.Ser120Leu, XP_047281977.1:p.Ser120Trp, NP_001257628.1:p.Ser120Leu, NP_001257628.1:p.Ser120Trp
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    rs1476088343 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      G>A [Show Flanks]
      Chromosome:
      10:31908769 (GRCh38)
      10:32197697 (GRCh37)
      Canonical SPDI:
      NC_000010.11:31908768:G:A
      Gene:
      ARHGAP12 (Varview)
      Functional Consequence:
      coding_sequence_variant,synonymous_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      A=0./0 (ALFA)
      A=0.000007/1 (GnomAD)
      A=0.000008/2 (GnomAD_exomes)
      HGVS:

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