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Links from Protein

Items: 1 to 20 of 389

1.

rs1489632585 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    TTC>- [Show Flanks]
    Chromosome:
    10:5949036 (GRCh38)
    10:5990999 (GRCh37)
    Canonical SPDI:
    NC_000010.11:5949029:TTCTTCTTC:TTCTTC
    Gene:
    IL15RA (Varview)
    Functional Consequence:
    3_prime_UTR_variant,inframe_deletion,coding_sequence_variant,downstream_transcript_variant,genic_downstream_transcript_variant
    HGVS:
    NC_000010.11:g.5949030TTC[2], NC_000010.10:g.5990993TTC[2], XM_011519461.3:c.1222GAA[2], XM_011519461.2:c.1222GAA[2], XM_011519461.1:c.1222GAA[2], XM_011519463.3:c.1123GAA[2], XM_011519463.2:c.1123GAA[2], XM_011519463.1:c.1123GAA[2], XM_011519464.3:c.1069GAA[2], XM_011519464.2:c.1069GAA[2], XM_011519464.1:c.1069GAA[2], XM_011519471.3:c.874GAA[2], XM_011519471.2:c.874GAA[2], XM_011519471.1:c.874GAA[2], XM_011519462.3:c.1153GAA[2], XM_011519462.2:c.1153GAA[2], XM_011519462.1:c.1153GAA[2], XM_017016197.3:c.787GAA[2], XM_017016197.2:c.787GAA[2], XM_017016197.1:c.787GAA[2], XM_011519474.3:c.775GAA[2], XM_011519474.2:c.775GAA[2], XM_011519474.1:c.775GAA[2], XM_011519467.3:c.1000GAA[2], XM_011519467.2:c.1000GAA[2], XM_011519467.1:c.1000GAA[2], XM_011519470.3:c.901GAA[2], XM_011519470.2:c.901GAA[2], XM_011519470.1:c.901GAA[2], XM_011519472.3:c.805GAA[2], XM_011519472.2:c.805GAA[2], XM_011519472.1:c.805GAA[2], XM_011519475.3:c.706GAA[2], XM_011519475.2:c.706GAA[2], XM_011519475.1:c.706GAA[2], XM_047425185.1:c.787GAA[2], XM_047425188.1:c.*252GAA[2], XP_011517763.1:p.Glu410del, XP_011517765.1:p.Glu377del, XP_011517766.1:p.Glu359del, XP_011517773.1:p.Glu294del, XP_011517764.1:p.Glu387del, XP_016871686.1:p.Glu265del, XP_011517776.1:p.Glu261del, XP_011517769.1:p.Glu336del, XP_011517772.1:p.Glu303del, XP_011517774.1:p.Glu271del, XP_011517777.1:p.Glu238del, XP_047281141.1:p.Glu265del

    2.

    rs1489067764 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      T>C [Show Flanks]
      Chromosome:
      10:5949137 (GRCh38)
      10:5991100 (GRCh37)
      Canonical SPDI:
      NC_000010.11:5949136:T:C
      Gene:
      IL15RA (Varview)
      Functional Consequence:
      3_prime_UTR_variant,genic_downstream_transcript_variant,missense_variant,coding_sequence_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      C=0.000174/4 (ALFA)
      C=0.000015/2 (GnomAD_exomes)
      C=0.000043/6 (GnomAD)
      C=0.000045/12 (TOPMED)
      HGVS:
      NC_000010.11:g.5949137T>C, NC_000010.10:g.5991100T>C, XM_011519461.3:c.1123A>G, XM_011519461.2:c.1123A>G, XM_011519461.1:c.1123A>G, XM_011519463.3:c.1024A>G, XM_011519463.2:c.1024A>G, XM_011519463.1:c.1024A>G, XM_011519464.3:c.970A>G, XM_011519464.2:c.970A>G, XM_011519464.1:c.970A>G, XM_011519471.3:c.775A>G, XM_011519471.2:c.775A>G, XM_011519471.1:c.775A>G, XM_011519462.3:c.1054A>G, XM_011519462.2:c.1054A>G, XM_011519462.1:c.1054A>G, XM_017016197.3:c.688A>G, XM_017016197.2:c.688A>G, XM_017016197.1:c.688A>G, XM_011519474.3:c.676A>G, XM_011519474.2:c.676A>G, XM_011519474.1:c.676A>G, XM_011519467.3:c.901A>G, XM_011519467.2:c.901A>G, XM_011519467.1:c.901A>G, XM_011519470.3:c.802A>G, XM_011519470.2:c.802A>G, XM_011519470.1:c.802A>G, XM_011519472.3:c.706A>G, XM_011519472.2:c.706A>G, XM_011519472.1:c.706A>G, XM_011519475.3:c.607A>G, XM_011519475.2:c.607A>G, XM_011519475.1:c.607A>G, XM_011519468.2:c.*153A>G, XM_011519468.1:c.*153A>G, XM_047425185.1:c.688A>G, XM_047425188.1:c.*153A>G, XP_011517763.1:p.Asn375Asp, XP_011517765.1:p.Asn342Asp, XP_011517766.1:p.Asn324Asp, XP_011517773.1:p.Asn259Asp, XP_011517764.1:p.Asn352Asp, XP_016871686.1:p.Asn230Asp, XP_011517776.1:p.Asn226Asp, XP_011517769.1:p.Asn301Asp, XP_011517772.1:p.Asn268Asp, XP_011517774.1:p.Asn236Asp, XP_011517777.1:p.Asn203Asp, XP_047281141.1:p.Asn230Asp

      3.

      rs1486576698 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        G>A,T [Show Flanks]
        Chromosome:
        10:5963837 (GRCh38)
        10:6005800 (GRCh37)
        Canonical SPDI:
        NC_000010.11:5963836:G:A,NC_000010.11:5963836:G:T
        Gene:
        IL15RA (Varview), LOC107984200 (Varview)
        Functional Consequence:
        coding_sequence_variant,missense_variant,intron_variant,synonymous_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        T=0./0 (ALFA)
        T=0.000004/1 (TOPMED)
        T=0.000007/1 (GnomAD)
        HGVS:
        NC_000010.11:g.5963837G>A, NC_000010.11:g.5963837G>T, NC_000010.10:g.6005800G>A, NC_000010.10:g.6005800G>T, NM_002189.4:c.288C>T, NM_002189.4:c.288C>A, NM_002189.3:c.288C>T, NM_002189.3:c.288C>A, XM_011519466.3:c.615C>T, XM_011519466.3:c.615C>A, XM_011519466.2:c.615C>T, XM_011519466.2:c.615C>A, XM_011519466.1:c.615C>T, XM_011519466.1:c.615C>A, XM_011519461.3:c.615C>T, XM_011519461.3:c.615C>A, XM_011519461.2:c.615C>T, XM_011519461.2:c.615C>A, XM_011519461.1:c.615C>T, XM_011519461.1:c.615C>A, XM_011519464.3:c.462C>T, XM_011519464.3:c.462C>A, XM_011519464.2:c.462C>T, XM_011519464.2:c.462C>A, XM_011519464.1:c.462C>T, XM_011519464.1:c.462C>A, XM_011519471.3:c.267C>T, XM_011519471.3:c.267C>A, XM_011519471.2:c.267C>T, XM_011519471.2:c.267C>A, XM_011519471.1:c.267C>T, XM_011519471.1:c.267C>A, XM_011519462.3:c.546C>T, XM_011519462.3:c.546C>A, XM_011519462.2:c.546C>T, XM_011519462.2:c.546C>A, XM_011519462.1:c.546C>T, XM_011519462.1:c.546C>A, XM_017016197.3:c.180C>T, XM_017016197.3:c.180C>A, XM_017016197.2:c.180C>T, XM_017016197.2:c.180C>A, XM_017016197.1:c.180C>T, XM_017016197.1:c.180C>A, XM_011519467.3:c.393C>T, XM_011519467.3:c.393C>A, XM_011519467.2:c.393C>T, XM_011519467.2:c.393C>A, XM_011519467.1:c.393C>T, XM_011519467.1:c.393C>A, XM_011519472.3:c.198C>T, XM_011519472.3:c.198C>A, XM_011519472.2:c.198C>T, XM_011519472.2:c.198C>A, XM_011519472.1:c.198C>T, XM_011519472.1:c.198C>A, XM_011519465.2:c.615C>T, XM_011519465.2:c.615C>A, XM_011519465.1:c.615C>T, XM_011519465.1:c.615C>A, XM_017016195.2:c.462C>T, XM_017016195.2:c.462C>A, XM_017016195.1:c.462C>T, XM_017016195.1:c.462C>A, XM_017016198.2:c.267C>T, XM_017016198.2:c.267C>A, XM_017016198.1:c.267C>T, XM_017016198.1:c.267C>A, NM_001243539.2:c.180C>T, NM_001243539.2:c.180C>A, NM_001243539.1:c.180C>T, NM_001243539.1:c.180C>A, XM_011519468.2:c.615C>T, XM_011519468.2:c.615C>A, XM_011519468.1:c.615C>T, XM_011519468.1:c.615C>A, XM_017016199.2:c.615C>T, XM_017016199.2:c.615C>A, XM_017016199.1:c.615C>T, XM_017016199.1:c.615C>A, XM_047425184.1:c.462C>T, XM_047425184.1:c.462C>A, XM_047425181.1:c.546C>T, XM_047425181.1:c.546C>A, NR_033494.1:n.603C>T, NR_033494.1:n.603C>A, XM_047425185.1:c.180C>T, XM_047425185.1:c.180C>A, NM_001351096.1:c.180C>T, NM_001351096.1:c.180C>A, NM_001256765.1:c.546C>T, NM_001256765.1:c.546C>A, XM_047425186.1:c.393C>T, XM_047425186.1:c.393C>A, XM_047425190.1:c.198C>T, XM_047425190.1:c.198C>A, XM_047425189.1:c.198C>T, XM_047425189.1:c.198C>A, NP_002180.1:p.Asp96Glu, XP_011517768.1:p.Asp205Glu, XP_011517763.1:p.Asp205Glu, XP_011517766.1:p.Asp154Glu, XP_011517773.1:p.Asp89Glu, XP_011517764.1:p.Asp182Glu, XP_016871686.1:p.Asp60Glu, XP_011517769.1:p.Asp131Glu, XP_011517774.1:p.Asp66Glu, XP_011517767.1:p.Asp205Glu, XP_016871684.1:p.Asp154Glu, XP_016871687.1:p.Asp89Glu, NP_001230468.1:p.Asp60Glu, XP_011517770.1:p.Asp205Glu, XP_016871688.1:p.Asp205Glu, XP_047281140.1:p.Asp154Glu, XP_047281137.1:p.Asp182Glu, XP_047281141.1:p.Asp60Glu, NP_001338025.1:p.Asp60Glu, NP_001243694.1:p.Asp182Glu, XP_047281142.1:p.Asp131Glu, XP_047281146.1:p.Asp66Glu, XP_047281145.1:p.Asp66Glu

        4.

        rs1481917651 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          G>A [Show Flanks]
          Chromosome:
          10:5960558 (GRCh38)
          10:6002521 (GRCh37)
          Canonical SPDI:
          NC_000010.11:5960557:G:A
          Gene:
          IL15RA (Varview), LOC107984200 (Varview)
          Functional Consequence:
          2KB_upstream_variant,downstream_transcript_variant,non_coding_transcript_variant,missense_variant,genic_downstream_transcript_variant,coding_sequence_variant,upstream_transcript_variant
          Validated:
          by frequency
          MAF:
          A=0.000004/1 (GnomAD_exomes)
          HGVS:
          NC_000010.11:g.5960558G>A, NC_000010.10:g.6002521G>A, NM_002189.4:c.392C>T, NM_002189.3:c.392C>T, XM_011519466.3:c.719C>T, XM_011519466.2:c.719C>T, XM_011519466.1:c.719C>T, XM_011519461.3:c.719C>T, XM_011519461.2:c.719C>T, XM_011519461.1:c.719C>T, XM_011519463.3:c.620C>T, XM_011519463.2:c.620C>T, XM_011519463.1:c.620C>T, XM_011519464.3:c.566C>T, XM_011519464.2:c.566C>T, XM_011519464.1:c.566C>T, XM_011519477.3:c.203C>T, XM_011519477.2:c.203C>T, XM_011519477.1:c.203C>T, NM_172200.3:c.293C>T, NM_172200.2:c.293C>T, XM_011519476.3:c.203C>T, XM_011519476.2:c.203C>T, XM_011519476.1:c.203C>T, XM_011519471.3:c.371C>T, XM_011519471.2:c.371C>T, XM_011519471.1:c.371C>T, XM_011519462.3:c.650C>T, XM_011519462.2:c.650C>T, XM_011519462.1:c.650C>T, XM_017016197.3:c.284C>T, XM_017016197.2:c.284C>T, XM_017016197.1:c.284C>T, XM_011519474.3:c.272C>T, XM_011519474.2:c.272C>T, XM_011519474.1:c.272C>T, XM_011519467.3:c.497C>T, XM_011519467.2:c.497C>T, XM_011519467.1:c.497C>T, XM_011519470.3:c.398C>T, XM_011519470.2:c.398C>T, XM_011519470.1:c.398C>T, XM_011519472.3:c.302C>T, XM_011519472.2:c.302C>T, XM_011519472.1:c.302C>T, XM_011519475.3:c.203C>T, XM_011519475.2:c.203C>T, XM_011519475.1:c.203C>T, XM_011519465.2:c.719C>T, XM_011519465.1:c.719C>T, XM_011519469.2:c.620C>T, XM_011519469.1:c.620C>T, NM_001351095.2:c.467C>T, NM_001351095.1:c.467C>T, XM_017016195.2:c.566C>T, XM_017016195.1:c.566C>T, XM_017016198.2:c.371C>T, XM_017016198.1:c.371C>T, NM_001243539.2:c.284C>T, NM_001243539.1:c.284C>T, NM_001351097.2:c.185C>T, NM_001351097.1:c.185C>T, XM_011519468.2:c.719C>T, XM_011519468.1:c.719C>T, NR_046362.2:n.280C>T, NR_046362.1:n.421C>T, XM_047425182.1:c.620C>T, XM_047425184.1:c.566C>T, XM_047425181.1:c.650C>T, NR_033494.1:n.707C>T, XM_047425185.1:c.284C>T, NM_001351096.1:c.284C>T, XM_047425191.1:c.272C>T, NM_001256765.1:c.650C>T, XM_047425186.1:c.497C>T, XM_047425183.1:c.551C>T, XM_047425187.1:c.398C>T, XM_047425190.1:c.302C>T, XM_047425189.1:c.302C>T, XM_047425188.1:c.398C>T, NP_002180.1:p.Ala131Val, XP_011517768.1:p.Ala240Val, XP_011517763.1:p.Ala240Val, XP_011517765.1:p.Ala207Val, XP_011517766.1:p.Ala189Val, XP_011517779.1:p.Ala68Val, NP_751950.2:p.Ala98Val, XP_011517778.1:p.Ala68Val, XP_011517773.1:p.Ala124Val, XP_011517764.1:p.Ala217Val, XP_016871686.1:p.Ala95Val, XP_011517776.1:p.Ala91Val, XP_011517769.1:p.Ala166Val, XP_011517772.1:p.Ala133Val, XP_011517774.1:p.Ala101Val, XP_011517777.1:p.Ala68Val, XP_011517767.1:p.Ala240Val, XP_011517771.1:p.Ala207Val, NP_001338024.1:p.Ala156Val, XP_016871684.1:p.Ala189Val, XP_016871687.1:p.Ala124Val, NP_001230468.1:p.Ala95Val, NP_001338026.1:p.Ala62Val, XP_011517770.1:p.Ala240Val, XP_047281138.1:p.Ala207Val, XP_047281140.1:p.Ala189Val, XP_047281137.1:p.Ala217Val, XP_047281141.1:p.Ala95Val, NP_001338025.1:p.Ala95Val, XP_047281147.1:p.Ala91Val, NP_001243694.1:p.Ala217Val, XP_047281142.1:p.Ala166Val, XP_047281139.1:p.Ala184Val, XP_047281143.1:p.Ala133Val, XP_047281146.1:p.Ala101Val, XP_047281145.1:p.Ala101Val, XP_047281144.1:p.Ala133Val

          5.

          rs1481866847 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            T>C [Show Flanks]
            Chromosome:
            10:5956449 (GRCh38)
            10:5998412 (GRCh37)
            Canonical SPDI:
            NC_000010.11:5956448:T:C
            Gene:
            IL15RA (Varview)
            Functional Consequence:
            coding_sequence_variant,missense_variant,non_coding_transcript_variant,genic_downstream_transcript_variant
            Validated:
            by frequency,by cluster
            MAF:
            C=0.000004/1 (GnomAD_exomes)
            HGVS:
            NC_000010.11:g.5956449T>C, NC_000010.10:g.5998412T>C, NM_002189.4:c.622A>G, NM_002189.3:c.622A>G, XM_011519466.3:c.949A>G, XM_011519466.2:c.949A>G, XM_011519466.1:c.949A>G, XM_011519461.3:c.949A>G, XM_011519461.2:c.949A>G, XM_011519461.1:c.949A>G, XM_011519463.3:c.850A>G, XM_011519463.2:c.850A>G, XM_011519463.1:c.850A>G, XM_011519464.3:c.796A>G, XM_011519464.2:c.796A>G, XM_011519464.1:c.796A>G, XM_011519477.3:c.433A>G, XM_011519477.2:c.433A>G, XM_011519477.1:c.433A>G, NM_172200.3:c.523A>G, NM_172200.2:c.523A>G, XM_011519476.3:c.433A>G, XM_011519476.2:c.433A>G, XM_011519476.1:c.433A>G, XM_011519471.3:c.601A>G, XM_011519471.2:c.601A>G, XM_011519471.1:c.601A>G, XM_011519462.3:c.880A>G, XM_011519462.2:c.880A>G, XM_011519462.1:c.880A>G, XM_017016197.3:c.514A>G, XM_017016197.2:c.514A>G, XM_017016197.1:c.514A>G, XM_011519474.3:c.502A>G, XM_011519474.2:c.502A>G, XM_011519474.1:c.502A>G, XM_011519467.3:c.727A>G, XM_011519467.2:c.727A>G, XM_011519467.1:c.727A>G, XM_011519470.3:c.628A>G, XM_011519470.2:c.628A>G, XM_011519470.1:c.628A>G, XM_011519472.3:c.532A>G, XM_011519472.2:c.532A>G, XM_011519472.1:c.532A>G, XM_011519475.3:c.433A>G, XM_011519475.2:c.433A>G, XM_011519475.1:c.433A>G, XM_011519465.2:c.949A>G, XM_011519465.1:c.949A>G, XM_011519469.2:c.850A>G, XM_011519469.1:c.850A>G, NM_001351095.2:c.697A>G, NM_001351095.1:c.697A>G, XM_017016195.2:c.796A>G, XM_017016195.1:c.796A>G, XM_017016198.2:c.601A>G, XM_017016198.1:c.601A>G, NM_001243539.2:c.514A>G, NM_001243539.1:c.514A>G, NM_001351097.2:c.415A>G, NM_001351097.1:c.415A>G, XM_011519468.2:c.949A>G, XM_011519468.1:c.949A>G, NR_046362.2:n.510A>G, NR_046362.1:n.651A>G, XM_047425182.1:c.850A>G, XM_047425184.1:c.796A>G, XM_047425181.1:c.880A>G, NR_033494.1:n.937A>G, XM_047425185.1:c.514A>G, NM_001351096.1:c.514A>G, XM_047425191.1:c.502A>G, NM_001256765.1:c.880A>G, XM_047425186.1:c.727A>G, XM_047425183.1:c.781A>G, XM_047425187.1:c.628A>G, XM_047425190.1:c.532A>G, XM_047425189.1:c.532A>G, XM_047425188.1:c.628A>G, NP_002180.1:p.Ile208Val, XP_011517768.1:p.Ile317Val, XP_011517763.1:p.Ile317Val, XP_011517765.1:p.Ile284Val, XP_011517766.1:p.Ile266Val, XP_011517779.1:p.Ile145Val, NP_751950.2:p.Ile175Val, XP_011517778.1:p.Ile145Val, XP_011517773.1:p.Ile201Val, XP_011517764.1:p.Ile294Val, XP_016871686.1:p.Ile172Val, XP_011517776.1:p.Ile168Val, XP_011517769.1:p.Ile243Val, XP_011517772.1:p.Ile210Val, XP_011517774.1:p.Ile178Val, XP_011517777.1:p.Ile145Val, XP_011517767.1:p.Ile317Val, XP_011517771.1:p.Ile284Val, NP_001338024.1:p.Ile233Val, XP_016871684.1:p.Ile266Val, XP_016871687.1:p.Ile201Val, NP_001230468.1:p.Ile172Val, NP_001338026.1:p.Ile139Val, XP_011517770.1:p.Ile317Val, XP_047281138.1:p.Ile284Val, XP_047281140.1:p.Ile266Val, XP_047281137.1:p.Ile294Val, XP_047281141.1:p.Ile172Val, NP_001338025.1:p.Ile172Val, XP_047281147.1:p.Ile168Val, NP_001243694.1:p.Ile294Val, XP_047281142.1:p.Ile243Val, XP_047281139.1:p.Ile261Val, XP_047281143.1:p.Ile210Val, XP_047281146.1:p.Ile178Val, XP_047281145.1:p.Ile178Val, XP_047281144.1:p.Ile210Val

            6.

            rs1480393723 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              G>A,C [Show Flanks]
              Chromosome:
              10:5966323 (GRCh38)
              10:6008286 (GRCh37)
              Canonical SPDI:
              NC_000010.11:5966322:G:A,NC_000010.11:5966322:G:C
              Gene:
              IL15RA (Varview), LOC107984200 (Varview)
              Functional Consequence:
              coding_sequence_variant,5_prime_UTR_variant,intron_variant,synonymous_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              C=0./0 (ALFA)
              A=0.000004/1 (GnomAD_exomes)
              C=0.000004/1 (TOPMED)
              C=0.000007/1 (GnomAD)
              HGVS:
              NC_000010.11:g.5966323G>A, NC_000010.11:g.5966323G>C, NC_000010.10:g.6008286G>A, NC_000010.10:g.6008286G>C, NM_002189.4:c.105C>T, NM_002189.4:c.105C>G, NM_002189.3:c.105C>T, NM_002189.3:c.105C>G, XM_011519466.3:c.432C>T, XM_011519466.3:c.432C>G, XM_011519466.2:c.432C>T, XM_011519466.2:c.432C>G, XM_011519466.1:c.432C>T, XM_011519466.1:c.432C>G, XM_011519461.3:c.432C>T, XM_011519461.3:c.432C>G, XM_011519461.2:c.432C>T, XM_011519461.2:c.432C>G, XM_011519461.1:c.432C>T, XM_011519461.1:c.432C>G, XM_011519463.3:c.432C>T, XM_011519463.3:c.432C>G, XM_011519463.2:c.432C>T, XM_011519463.2:c.432C>G, XM_011519463.1:c.432C>T, XM_011519463.1:c.432C>G, XM_011519464.3:c.279C>T, XM_011519464.3:c.279C>G, XM_011519464.2:c.279C>T, XM_011519464.2:c.279C>G, XM_011519464.1:c.279C>T, XM_011519464.1:c.279C>G, NM_172200.3:c.105C>T, NM_172200.3:c.105C>G, NM_172200.2:c.105C>T, NM_172200.2:c.105C>G, XM_011519462.3:c.363C>T, XM_011519462.3:c.363C>G, XM_011519462.2:c.363C>T, XM_011519462.2:c.363C>G, XM_011519462.1:c.363C>T, XM_011519462.1:c.363C>G, XM_017016197.3:c.-4C>T, XM_017016197.3:c.-4C>G, XM_017016197.2:c.-4C>T, XM_017016197.2:c.-4C>G, XM_017016197.1:c.-4C>T, XM_017016197.1:c.-4C>G, XM_011519467.3:c.210C>T, XM_011519467.3:c.210C>G, XM_011519467.2:c.210C>T, XM_011519467.2:c.210C>G, XM_011519467.1:c.210C>T, XM_011519467.1:c.210C>G, XM_011519470.3:c.210C>T, XM_011519470.3:c.210C>G, XM_011519470.2:c.210C>T, XM_011519470.2:c.210C>G, XM_011519470.1:c.210C>T, XM_011519470.1:c.210C>G, XM_011519465.2:c.432C>T, XM_011519465.2:c.432C>G, XM_011519465.1:c.432C>T, XM_011519465.1:c.432C>G, XM_011519469.2:c.432C>T, XM_011519469.2:c.432C>G, XM_011519469.1:c.432C>T, XM_011519469.1:c.432C>G, NM_001351095.2:c.279C>T, NM_001351095.2:c.279C>G, NM_001351095.1:c.279C>T, NM_001351095.1:c.279C>G, XM_017016195.2:c.279C>T, XM_017016195.2:c.279C>G, XM_017016195.1:c.279C>T, XM_017016195.1:c.279C>G, NM_001243539.2:c.-4C>T, NM_001243539.2:c.-4C>G, NM_001243539.1:c.-4C>T, NM_001243539.1:c.-4C>G, NM_001351097.2:c.-4C>T, NM_001351097.2:c.-4C>G, NM_001351097.1:c.-4C>T, NM_001351097.1:c.-4C>G, XM_011519468.2:c.432C>T, XM_011519468.2:c.432C>G, XM_011519468.1:c.432C>T, XM_011519468.1:c.432C>G, XM_017016199.2:c.432C>T, XM_017016199.2:c.432C>G, XM_017016199.1:c.432C>T, XM_017016199.1:c.432C>G, XM_047425182.1:c.432C>T, XM_047425182.1:c.432C>G, XM_047425184.1:c.279C>T, XM_047425184.1:c.279C>G, XM_047425181.1:c.363C>T, XM_047425181.1:c.363C>G, NR_033494.1:n.420C>T, NR_033494.1:n.420C>G, XM_047425185.1:c.-4C>T, XM_047425185.1:c.-4C>G, NM_001351096.1:c.-4C>T, NM_001351096.1:c.-4C>G, NM_001256765.1:c.363C>T, NM_001256765.1:c.363C>G, XM_047425186.1:c.210C>T, XM_047425186.1:c.210C>G, XM_047425183.1:c.363C>T, XM_047425183.1:c.363C>G, XM_047425187.1:c.210C>T, XM_047425187.1:c.210C>G, XM_047425188.1:c.210C>T, XM_047425188.1:c.210C>G

              7.

              rs1476164301 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                G>A [Show Flanks]
                Chromosome:
                10:5963777 (GRCh38)
                10:6005740 (GRCh37)
                Canonical SPDI:
                NC_000010.11:5963776:G:A
                Gene:
                IL15RA (Varview), LOC107984200 (Varview)
                Functional Consequence:
                coding_sequence_variant,intron_variant,synonymous_variant
                HGVS:
                NC_000010.11:g.5963777G>A, NC_000010.10:g.6005740G>A, NM_002189.4:c.348C>T, NM_002189.3:c.348C>T, XM_011519466.3:c.675C>T, XM_011519466.2:c.675C>T, XM_011519466.1:c.675C>T, XM_011519461.3:c.675C>T, XM_011519461.2:c.675C>T, XM_011519461.1:c.675C>T, XM_011519464.3:c.522C>T, XM_011519464.2:c.522C>T, XM_011519464.1:c.522C>T, XM_011519471.3:c.327C>T, XM_011519471.2:c.327C>T, XM_011519471.1:c.327C>T, XM_011519462.3:c.606C>T, XM_011519462.2:c.606C>T, XM_011519462.1:c.606C>T, XM_017016197.3:c.240C>T, XM_017016197.2:c.240C>T, XM_017016197.1:c.240C>T, XM_011519467.3:c.453C>T, XM_011519467.2:c.453C>T, XM_011519467.1:c.453C>T, XM_011519472.3:c.258C>T, XM_011519472.2:c.258C>T, XM_011519472.1:c.258C>T, XM_011519465.2:c.675C>T, XM_011519465.1:c.675C>T, XM_017016195.2:c.522C>T, XM_017016195.1:c.522C>T, XM_017016198.2:c.327C>T, XM_017016198.1:c.327C>T, NM_001243539.2:c.240C>T, NM_001243539.1:c.240C>T, XM_011519468.2:c.675C>T, XM_011519468.1:c.675C>T, XM_017016199.2:c.675C>T, XM_017016199.1:c.675C>T, XM_047425184.1:c.522C>T, XM_047425181.1:c.606C>T, NR_033494.1:n.663C>T, XM_047425185.1:c.240C>T, NM_001351096.1:c.240C>T, NM_001256765.1:c.606C>T, XM_047425186.1:c.453C>T, XM_047425190.1:c.258C>T, XM_047425189.1:c.258C>T

                8.

                rs1473820827 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  A>G [Show Flanks]
                  Chromosome:
                  10:5948957 (GRCh38)
                  10:5990920 (GRCh37)
                  Canonical SPDI:
                  NC_000010.11:5948956:A:G
                  Gene:
                  IL15RA (Varview)
                  Functional Consequence:
                  3_prime_UTR_variant,stop_lost,downstream_transcript_variant,terminator_codon_variant,genic_downstream_transcript_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  G=0./0 (ALFA)
                  G=0.000004/1 (TOPMED)
                  G=0.000007/1 (GnomAD)
                  G=0.000019/1 (GnomAD_exomes)
                  HGVS:
                  NC_000010.11:g.5948957A>G, NC_000010.10:g.5990920A>G, XM_011519461.3:c.1303T>C, XM_011519461.2:c.1303T>C, XM_011519461.1:c.1303T>C, XM_011519463.3:c.1204T>C, XM_011519463.2:c.1204T>C, XM_011519463.1:c.1204T>C, XM_011519464.3:c.1150T>C, XM_011519464.2:c.1150T>C, XM_011519464.1:c.1150T>C, XM_011519471.3:c.955T>C, XM_011519471.2:c.955T>C, XM_011519471.1:c.955T>C, XM_011519462.3:c.1234T>C, XM_011519462.2:c.1234T>C, XM_011519462.1:c.1234T>C, XM_017016197.3:c.868T>C, XM_017016197.2:c.868T>C, XM_017016197.1:c.868T>C, XM_011519474.3:c.856T>C, XM_011519474.2:c.856T>C, XM_011519474.1:c.856T>C, XM_011519467.3:c.1081T>C, XM_011519467.2:c.1081T>C, XM_011519467.1:c.1081T>C, XM_011519470.3:c.982T>C, XM_011519470.2:c.982T>C, XM_011519470.1:c.982T>C, XM_011519472.3:c.886T>C, XM_011519472.2:c.886T>C, XM_011519472.1:c.886T>C, XM_011519475.3:c.787T>C, XM_011519475.2:c.787T>C, XM_011519475.1:c.787T>C, XM_047425185.1:c.868T>C, XM_047425188.1:c.*333T>C, XP_011517763.1:p.Ter435Arg, XP_011517765.1:p.Ter402Arg, XP_011517766.1:p.Ter384Arg, XP_011517773.1:p.Ter319Arg, XP_011517764.1:p.Ter412Arg, XP_016871686.1:p.Ter290Arg, XP_011517776.1:p.Ter286Arg, XP_011517769.1:p.Ter361Arg, XP_011517772.1:p.Ter328Arg, XP_011517774.1:p.Ter296Arg, XP_011517777.1:p.Ter263Arg, XP_047281141.1:p.Ter290Arg

                  9.

                  rs1473461417 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    A>G [Show Flanks]
                    Chromosome:
                    10:5977510 (GRCh38)
                    10:6019473 (GRCh37)
                    Canonical SPDI:
                    NC_000010.11:5977509:A:G
                    Gene:
                    IL15RA (Varview)
                    Functional Consequence:
                    coding_sequence_variant,genic_upstream_transcript_variant,5_prime_UTR_variant,missense_variant,intron_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    G=0./0 (ALFA)
                    G=0.000007/1 (GnomAD)
                    G=0.000008/2 (TOPMED)
                    HGVS:
                    NC_000010.11:g.5977510A>G, NC_000010.10:g.6019473A>G, NM_002189.4:c.-18T>C, NM_002189.3:c.-18T>C, XM_011519477.3:c.88T>C, XM_011519477.2:c.88T>C, XM_011519477.1:c.88T>C, NM_172200.3:c.-18T>C, NM_172200.2:c.-18T>C, XM_011519476.3:c.88T>C, XM_011519476.2:c.88T>C, XM_011519476.1:c.88T>C, XM_011519462.3:c.88T>C, XM_011519462.2:c.88T>C, XM_011519462.1:c.88T>C, XM_011519467.3:c.88T>C, XM_011519467.2:c.88T>C, XM_011519467.1:c.88T>C, XM_011519470.3:c.88T>C, XM_011519470.2:c.88T>C, XM_011519470.1:c.88T>C, XM_011519472.3:c.88T>C, XM_011519472.2:c.88T>C, XM_011519472.1:c.88T>C, XM_011519475.3:c.88T>C, XM_011519475.2:c.88T>C, XM_011519475.1:c.88T>C, XM_047425181.1:c.88T>C, NM_001256765.1:c.88T>C, XM_047425186.1:c.88T>C, XM_047425183.1:c.88T>C, XM_047425187.1:c.88T>C, XM_047425190.1:c.88T>C, XM_047425189.1:c.88T>C, XM_047425188.1:c.88T>C, XP_011517779.1:p.Ser30Pro, XP_011517778.1:p.Ser30Pro, XP_011517764.1:p.Ser30Pro, XP_011517769.1:p.Ser30Pro, XP_011517772.1:p.Ser30Pro, XP_011517774.1:p.Ser30Pro, XP_011517777.1:p.Ser30Pro, XP_047281137.1:p.Ser30Pro, NP_001243694.1:p.Ser30Pro, XP_047281142.1:p.Ser30Pro, XP_047281139.1:p.Ser30Pro, XP_047281143.1:p.Ser30Pro, XP_047281146.1:p.Ser30Pro, XP_047281145.1:p.Ser30Pro, XP_047281144.1:p.Ser30Pro

                    10.

                    rs1471910652 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      A>G,T [Show Flanks]
                      Chromosome:
                      10:5960439 (GRCh38)
                      10:6002402 (GRCh37)
                      Canonical SPDI:
                      NC_000010.11:5960438:A:G,NC_000010.11:5960438:A:T
                      Gene:
                      IL15RA (Varview), LOC107984200 (Varview)
                      Functional Consequence:
                      upstream_transcript_variant,coding_sequence_variant,non_coding_transcript_variant,downstream_transcript_variant,genic_downstream_transcript_variant,missense_variant,2KB_upstream_variant
                      Validated:
                      by frequency,by cluster
                      MAF:
                      T=0.000004/1 (GnomAD_exomes)
                      A=0.5/1 (SGDP_PRJ)
                      HGVS:
                      NC_000010.11:g.5960439A>G, NC_000010.11:g.5960439A>T, NC_000010.10:g.6002402A>G, NC_000010.10:g.6002402A>T, NM_002189.4:c.511T>C, NM_002189.4:c.511T>A, NM_002189.3:c.511T>C, NM_002189.3:c.511T>A, XM_011519466.3:c.838T>C, XM_011519466.3:c.838T>A, XM_011519466.2:c.838T>C, XM_011519466.2:c.838T>A, XM_011519466.1:c.838T>C, XM_011519466.1:c.838T>A, XM_011519461.3:c.838T>C, XM_011519461.3:c.838T>A, XM_011519461.2:c.838T>C, XM_011519461.2:c.838T>A, XM_011519461.1:c.838T>C, XM_011519461.1:c.838T>A, XM_011519463.3:c.739T>C, XM_011519463.3:c.739T>A, XM_011519463.2:c.739T>C, XM_011519463.2:c.739T>A, XM_011519463.1:c.739T>C, XM_011519463.1:c.739T>A, XM_011519464.3:c.685T>C, XM_011519464.3:c.685T>A, XM_011519464.2:c.685T>C, XM_011519464.2:c.685T>A, XM_011519464.1:c.685T>C, XM_011519464.1:c.685T>A, XM_011519477.3:c.322T>C, XM_011519477.3:c.322T>A, XM_011519477.2:c.322T>C, XM_011519477.2:c.322T>A, XM_011519477.1:c.322T>C, XM_011519477.1:c.322T>A, NM_172200.3:c.412T>C, NM_172200.3:c.412T>A, NM_172200.2:c.412T>C, NM_172200.2:c.412T>A, XM_011519476.3:c.322T>C, XM_011519476.3:c.322T>A, XM_011519476.2:c.322T>C, XM_011519476.2:c.322T>A, XM_011519476.1:c.322T>C, XM_011519476.1:c.322T>A, XM_011519471.3:c.490T>C, XM_011519471.3:c.490T>A, XM_011519471.2:c.490T>C, XM_011519471.2:c.490T>A, XM_011519471.1:c.490T>C, XM_011519471.1:c.490T>A, XM_011519462.3:c.769T>C, XM_011519462.3:c.769T>A, XM_011519462.2:c.769T>C, XM_011519462.2:c.769T>A, XM_011519462.1:c.769T>C, XM_011519462.1:c.769T>A, XM_017016197.3:c.403T>C, XM_017016197.3:c.403T>A, XM_017016197.2:c.403T>C, XM_017016197.2:c.403T>A, XM_017016197.1:c.403T>C, XM_017016197.1:c.403T>A, XM_011519474.3:c.391T>C, XM_011519474.3:c.391T>A, XM_011519474.2:c.391T>C, XM_011519474.2:c.391T>A, XM_011519474.1:c.391T>C, XM_011519474.1:c.391T>A, XM_011519467.3:c.616T>C, XM_011519467.3:c.616T>A, XM_011519467.2:c.616T>C, XM_011519467.2:c.616T>A, XM_011519467.1:c.616T>C, XM_011519467.1:c.616T>A, XM_011519470.3:c.517T>C, XM_011519470.3:c.517T>A, XM_011519470.2:c.517T>C, XM_011519470.2:c.517T>A, XM_011519470.1:c.517T>C, XM_011519470.1:c.517T>A, XM_011519472.3:c.421T>C, XM_011519472.3:c.421T>A, XM_011519472.2:c.421T>C, XM_011519472.2:c.421T>A, XM_011519472.1:c.421T>C, XM_011519472.1:c.421T>A, XM_011519475.3:c.322T>C, XM_011519475.3:c.322T>A, XM_011519475.2:c.322T>C, XM_011519475.2:c.322T>A, XM_011519475.1:c.322T>C, XM_011519475.1:c.322T>A, XM_011519465.2:c.838T>C, XM_011519465.2:c.838T>A, XM_011519465.1:c.838T>C, XM_011519465.1:c.838T>A, XM_011519469.2:c.739T>C, XM_011519469.2:c.739T>A, XM_011519469.1:c.739T>C, XM_011519469.1:c.739T>A, NM_001351095.2:c.586T>C, NM_001351095.2:c.586T>A, NM_001351095.1:c.586T>C, NM_001351095.1:c.586T>A, XM_017016195.2:c.685T>C, XM_017016195.2:c.685T>A, XM_017016195.1:c.685T>C, XM_017016195.1:c.685T>A, XM_017016198.2:c.490T>C, XM_017016198.2:c.490T>A, XM_017016198.1:c.490T>C, XM_017016198.1:c.490T>A, NM_001243539.2:c.403T>C, NM_001243539.2:c.403T>A, NM_001243539.1:c.403T>C, NM_001243539.1:c.403T>A, NM_001351097.2:c.304T>C, NM_001351097.2:c.304T>A, NM_001351097.1:c.304T>C, NM_001351097.1:c.304T>A, XM_011519468.2:c.838T>C, XM_011519468.2:c.838T>A, XM_011519468.1:c.838T>C, XM_011519468.1:c.838T>A, NR_046362.2:n.399T>C, NR_046362.2:n.399T>A, NR_046362.1:n.540T>C, NR_046362.1:n.540T>A, XM_047425182.1:c.739T>C, XM_047425182.1:c.739T>A, XM_047425184.1:c.685T>C, XM_047425184.1:c.685T>A, XM_047425181.1:c.769T>C, XM_047425181.1:c.769T>A, NR_033494.1:n.826T>C, NR_033494.1:n.826T>A, XM_047425185.1:c.403T>C, XM_047425185.1:c.403T>A, NM_001351096.1:c.403T>C, NM_001351096.1:c.403T>A, XM_047425191.1:c.391T>C, XM_047425191.1:c.391T>A, NM_001256765.1:c.769T>C, NM_001256765.1:c.769T>A, XM_047425186.1:c.616T>C, XM_047425186.1:c.616T>A, XM_047425183.1:c.670T>C, XM_047425183.1:c.670T>A, XM_047425187.1:c.517T>C, XM_047425187.1:c.517T>A, XM_047425190.1:c.421T>C, XM_047425190.1:c.421T>A, XM_047425189.1:c.421T>C, XM_047425189.1:c.421T>A, XM_047425188.1:c.517T>C, XM_047425188.1:c.517T>A, NP_002180.1:p.Ser171Pro, NP_002180.1:p.Ser171Thr, XP_011517768.1:p.Ser280Pro, XP_011517768.1:p.Ser280Thr, XP_011517763.1:p.Ser280Pro, XP_011517763.1:p.Ser280Thr, XP_011517765.1:p.Ser247Pro, XP_011517765.1:p.Ser247Thr, XP_011517766.1:p.Ser229Pro, XP_011517766.1:p.Ser229Thr, XP_011517779.1:p.Ser108Pro, XP_011517779.1:p.Ser108Thr, NP_751950.2:p.Ser138Pro, NP_751950.2:p.Ser138Thr, XP_011517778.1:p.Ser108Pro, XP_011517778.1:p.Ser108Thr, XP_011517773.1:p.Ser164Pro, XP_011517773.1:p.Ser164Thr, XP_011517764.1:p.Ser257Pro, XP_011517764.1:p.Ser257Thr, XP_016871686.1:p.Ser135Pro, XP_016871686.1:p.Ser135Thr, XP_011517776.1:p.Ser131Pro, XP_011517776.1:p.Ser131Thr, XP_011517769.1:p.Ser206Pro, XP_011517769.1:p.Ser206Thr, XP_011517772.1:p.Ser173Pro, XP_011517772.1:p.Ser173Thr, XP_011517774.1:p.Ser141Pro, XP_011517774.1:p.Ser141Thr, XP_011517777.1:p.Ser108Pro, XP_011517777.1:p.Ser108Thr, XP_011517767.1:p.Ser280Pro, XP_011517767.1:p.Ser280Thr, XP_011517771.1:p.Ser247Pro, XP_011517771.1:p.Ser247Thr, NP_001338024.1:p.Ser196Pro, NP_001338024.1:p.Ser196Thr, XP_016871684.1:p.Ser229Pro, XP_016871684.1:p.Ser229Thr, XP_016871687.1:p.Ser164Pro, XP_016871687.1:p.Ser164Thr, NP_001230468.1:p.Ser135Pro, NP_001230468.1:p.Ser135Thr, NP_001338026.1:p.Ser102Pro, NP_001338026.1:p.Ser102Thr, XP_011517770.1:p.Ser280Pro, XP_011517770.1:p.Ser280Thr, XP_047281138.1:p.Ser247Pro, XP_047281138.1:p.Ser247Thr, XP_047281140.1:p.Ser229Pro, XP_047281140.1:p.Ser229Thr, XP_047281137.1:p.Ser257Pro, XP_047281137.1:p.Ser257Thr, XP_047281141.1:p.Ser135Pro, XP_047281141.1:p.Ser135Thr, NP_001338025.1:p.Ser135Pro, NP_001338025.1:p.Ser135Thr, XP_047281147.1:p.Ser131Pro, XP_047281147.1:p.Ser131Thr, NP_001243694.1:p.Ser257Pro, NP_001243694.1:p.Ser257Thr, XP_047281142.1:p.Ser206Pro, XP_047281142.1:p.Ser206Thr, XP_047281139.1:p.Ser224Pro, XP_047281139.1:p.Ser224Thr, XP_047281143.1:p.Ser173Pro, XP_047281143.1:p.Ser173Thr, XP_047281146.1:p.Ser141Pro, XP_047281146.1:p.Ser141Thr, XP_047281145.1:p.Ser141Pro, XP_047281145.1:p.Ser141Thr, XP_047281144.1:p.Ser173Pro, XP_047281144.1:p.Ser173Thr

                      11.

                      rs1471039577 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        C>T [Show Flanks]
                        Chromosome:
                        10:5956410 (GRCh38)
                        10:5998373 (GRCh37)
                        Canonical SPDI:
                        NC_000010.11:5956409:C:T
                        Gene:
                        IL15RA (Varview)
                        Functional Consequence:
                        coding_sequence_variant,missense_variant,non_coding_transcript_variant,genic_downstream_transcript_variant
                        Validated:
                        by frequency,by alfa
                        MAF:
                        T=0./0 (ALFA)
                        T=0.000004/1 (TOPMED)
                        HGVS:
                        NC_000010.11:g.5956410C>T, NC_000010.10:g.5998373C>T, NM_002189.4:c.661G>A, NM_002189.3:c.661G>A, XM_011519466.3:c.988G>A, XM_011519466.2:c.988G>A, XM_011519466.1:c.988G>A, XM_011519461.3:c.988G>A, XM_011519461.2:c.988G>A, XM_011519461.1:c.988G>A, XM_011519463.3:c.889G>A, XM_011519463.2:c.889G>A, XM_011519463.1:c.889G>A, XM_011519464.3:c.835G>A, XM_011519464.2:c.835G>A, XM_011519464.1:c.835G>A, XM_011519477.3:c.472G>A, XM_011519477.2:c.472G>A, XM_011519477.1:c.472G>A, NM_172200.3:c.562G>A, NM_172200.2:c.562G>A, XM_011519476.3:c.472G>A, XM_011519476.2:c.472G>A, XM_011519476.1:c.472G>A, XM_011519471.3:c.640G>A, XM_011519471.2:c.640G>A, XM_011519471.1:c.640G>A, XM_011519462.3:c.919G>A, XM_011519462.2:c.919G>A, XM_011519462.1:c.919G>A, XM_017016197.3:c.553G>A, XM_017016197.2:c.553G>A, XM_017016197.1:c.553G>A, XM_011519474.3:c.541G>A, XM_011519474.2:c.541G>A, XM_011519474.1:c.541G>A, XM_011519467.3:c.766G>A, XM_011519467.2:c.766G>A, XM_011519467.1:c.766G>A, XM_011519470.3:c.667G>A, XM_011519470.2:c.667G>A, XM_011519470.1:c.667G>A, XM_011519472.3:c.571G>A, XM_011519472.2:c.571G>A, XM_011519472.1:c.571G>A, XM_011519475.3:c.472G>A, XM_011519475.2:c.472G>A, XM_011519475.1:c.472G>A, XM_011519465.2:c.988G>A, XM_011519465.1:c.988G>A, XM_011519469.2:c.889G>A, XM_011519469.1:c.889G>A, NM_001351095.2:c.736G>A, NM_001351095.1:c.736G>A, XM_017016195.2:c.835G>A, XM_017016195.1:c.835G>A, XM_017016198.2:c.640G>A, XM_017016198.1:c.640G>A, NM_001243539.2:c.553G>A, NM_001243539.1:c.553G>A, NM_001351097.2:c.454G>A, NM_001351097.1:c.454G>A, XM_011519468.2:c.988G>A, XM_011519468.1:c.988G>A, NR_046362.2:n.549G>A, NR_046362.1:n.690G>A, XM_047425182.1:c.889G>A, XM_047425184.1:c.835G>A, XM_047425181.1:c.919G>A, NR_033494.1:n.976G>A, XM_047425185.1:c.553G>A, NM_001351096.1:c.553G>A, XM_047425191.1:c.541G>A, NM_001256765.1:c.919G>A, XM_047425186.1:c.766G>A, XM_047425183.1:c.820G>A, XM_047425187.1:c.667G>A, XM_047425190.1:c.571G>A, XM_047425189.1:c.571G>A, XM_047425188.1:c.667G>A, NP_002180.1:p.Val221Met, XP_011517768.1:p.Val330Met, XP_011517763.1:p.Val330Met, XP_011517765.1:p.Val297Met, XP_011517766.1:p.Val279Met, XP_011517779.1:p.Val158Met, NP_751950.2:p.Val188Met, XP_011517778.1:p.Val158Met, XP_011517773.1:p.Val214Met, XP_011517764.1:p.Val307Met, XP_016871686.1:p.Val185Met, XP_011517776.1:p.Val181Met, XP_011517769.1:p.Val256Met, XP_011517772.1:p.Val223Met, XP_011517774.1:p.Val191Met, XP_011517777.1:p.Val158Met, XP_011517767.1:p.Val330Met, XP_011517771.1:p.Val297Met, NP_001338024.1:p.Val246Met, XP_016871684.1:p.Val279Met, XP_016871687.1:p.Val214Met, NP_001230468.1:p.Val185Met, NP_001338026.1:p.Val152Met, XP_011517770.1:p.Val330Met, XP_047281138.1:p.Val297Met, XP_047281140.1:p.Val279Met, XP_047281137.1:p.Val307Met, XP_047281141.1:p.Val185Met, NP_001338025.1:p.Val185Met, XP_047281147.1:p.Val181Met, NP_001243694.1:p.Val307Met, XP_047281142.1:p.Val256Met, XP_047281139.1:p.Val274Met, XP_047281143.1:p.Val223Met, XP_047281146.1:p.Val191Met, XP_047281145.1:p.Val191Met, XP_047281144.1:p.Val223Met

                        12.

                        rs1469028404 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          G>A,C,T [Show Flanks]
                          Chromosome:
                          10:5960564 (GRCh38)
                          10:6002527 (GRCh37)
                          Canonical SPDI:
                          NC_000010.11:5960563:G:A,NC_000010.11:5960563:G:C,NC_000010.11:5960563:G:T
                          Gene:
                          IL15RA (Varview), LOC107984200 (Varview)
                          Functional Consequence:
                          upstream_transcript_variant,coding_sequence_variant,non_coding_transcript_variant,downstream_transcript_variant,genic_downstream_transcript_variant,missense_variant,2KB_upstream_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          C=0./0 (ALFA)
                          C=0.000004/1 (GnomAD_exomes)
                          C=0.000008/2 (TOPMED)
                          C=0.000014/2 (GnomAD)
                          HGVS:
                          NC_000010.11:g.5960564G>A, NC_000010.11:g.5960564G>C, NC_000010.11:g.5960564G>T, NC_000010.10:g.6002527G>A, NC_000010.10:g.6002527G>C, NC_000010.10:g.6002527G>T, NM_002189.4:c.386C>T, NM_002189.4:c.386C>G, NM_002189.4:c.386C>A, NM_002189.3:c.386C>T, NM_002189.3:c.386C>G, NM_002189.3:c.386C>A, XM_011519466.3:c.713C>T, XM_011519466.3:c.713C>G, XM_011519466.3:c.713C>A, XM_011519466.2:c.713C>T, XM_011519466.2:c.713C>G, XM_011519466.2:c.713C>A, XM_011519466.1:c.713C>T, XM_011519466.1:c.713C>G, XM_011519466.1:c.713C>A, XM_011519461.3:c.713C>T, XM_011519461.3:c.713C>G, XM_011519461.3:c.713C>A, XM_011519461.2:c.713C>T, XM_011519461.2:c.713C>G, XM_011519461.2:c.713C>A, XM_011519461.1:c.713C>T, XM_011519461.1:c.713C>G, XM_011519461.1:c.713C>A, XM_011519463.3:c.614C>T, XM_011519463.3:c.614C>G, XM_011519463.3:c.614C>A, XM_011519463.2:c.614C>T, XM_011519463.2:c.614C>G, XM_011519463.2:c.614C>A, XM_011519463.1:c.614C>T, XM_011519463.1:c.614C>G, XM_011519463.1:c.614C>A, XM_011519464.3:c.560C>T, XM_011519464.3:c.560C>G, XM_011519464.3:c.560C>A, XM_011519464.2:c.560C>T, XM_011519464.2:c.560C>G, XM_011519464.2:c.560C>A, XM_011519464.1:c.560C>T, XM_011519464.1:c.560C>G, XM_011519464.1:c.560C>A, XM_011519477.3:c.197C>T, XM_011519477.3:c.197C>G, XM_011519477.3:c.197C>A, XM_011519477.2:c.197C>T, XM_011519477.2:c.197C>G, XM_011519477.2:c.197C>A, XM_011519477.1:c.197C>T, XM_011519477.1:c.197C>G, XM_011519477.1:c.197C>A, NM_172200.3:c.287C>T, NM_172200.3:c.287C>G, NM_172200.3:c.287C>A, NM_172200.2:c.287C>T, NM_172200.2:c.287C>G, NM_172200.2:c.287C>A, XM_011519476.3:c.197C>T, XM_011519476.3:c.197C>G, XM_011519476.3:c.197C>A, XM_011519476.2:c.197C>T, XM_011519476.2:c.197C>G, XM_011519476.2:c.197C>A, XM_011519476.1:c.197C>T, XM_011519476.1:c.197C>G, XM_011519476.1:c.197C>A, XM_011519471.3:c.365C>T, XM_011519471.3:c.365C>G, XM_011519471.3:c.365C>A, XM_011519471.2:c.365C>T, XM_011519471.2:c.365C>G, XM_011519471.2:c.365C>A, XM_011519471.1:c.365C>T, XM_011519471.1:c.365C>G, XM_011519471.1:c.365C>A, XM_011519462.3:c.644C>T, XM_011519462.3:c.644C>G, XM_011519462.3:c.644C>A, XM_011519462.2:c.644C>T, XM_011519462.2:c.644C>G, XM_011519462.2:c.644C>A, XM_011519462.1:c.644C>T, XM_011519462.1:c.644C>G, XM_011519462.1:c.644C>A, XM_017016197.3:c.278C>T, XM_017016197.3:c.278C>G, XM_017016197.3:c.278C>A, XM_017016197.2:c.278C>T, XM_017016197.2:c.278C>G, XM_017016197.2:c.278C>A, XM_017016197.1:c.278C>T, XM_017016197.1:c.278C>G, XM_017016197.1:c.278C>A, XM_011519474.3:c.266C>T, XM_011519474.3:c.266C>G, XM_011519474.3:c.266C>A, XM_011519474.2:c.266C>T, XM_011519474.2:c.266C>G, XM_011519474.2:c.266C>A, XM_011519474.1:c.266C>T, XM_011519474.1:c.266C>G, XM_011519474.1:c.266C>A, XM_011519467.3:c.491C>T, XM_011519467.3:c.491C>G, XM_011519467.3:c.491C>A, XM_011519467.2:c.491C>T, XM_011519467.2:c.491C>G, XM_011519467.2:c.491C>A, XM_011519467.1:c.491C>T, XM_011519467.1:c.491C>G, XM_011519467.1:c.491C>A, XM_011519470.3:c.392C>T, XM_011519470.3:c.392C>G, XM_011519470.3:c.392C>A, XM_011519470.2:c.392C>T, XM_011519470.2:c.392C>G, XM_011519470.2:c.392C>A, XM_011519470.1:c.392C>T, XM_011519470.1:c.392C>G, XM_011519470.1:c.392C>A, XM_011519472.3:c.296C>T, XM_011519472.3:c.296C>G, XM_011519472.3:c.296C>A, XM_011519472.2:c.296C>T, XM_011519472.2:c.296C>G, XM_011519472.2:c.296C>A, XM_011519472.1:c.296C>T, XM_011519472.1:c.296C>G, XM_011519472.1:c.296C>A, XM_011519475.3:c.197C>T, XM_011519475.3:c.197C>G, XM_011519475.3:c.197C>A, XM_011519475.2:c.197C>T, XM_011519475.2:c.197C>G, XM_011519475.2:c.197C>A, XM_011519475.1:c.197C>T, XM_011519475.1:c.197C>G, XM_011519475.1:c.197C>A, XM_011519465.2:c.713C>T, XM_011519465.2:c.713C>G, XM_011519465.2:c.713C>A, XM_011519465.1:c.713C>T, XM_011519465.1:c.713C>G, XM_011519465.1:c.713C>A, XM_011519469.2:c.614C>T, XM_011519469.2:c.614C>G, XM_011519469.2:c.614C>A, XM_011519469.1:c.614C>T, XM_011519469.1:c.614C>G, XM_011519469.1:c.614C>A, NM_001351095.2:c.461C>T, NM_001351095.2:c.461C>G, NM_001351095.2:c.461C>A, NM_001351095.1:c.461C>T, NM_001351095.1:c.461C>G, NM_001351095.1:c.461C>A, XM_017016195.2:c.560C>T, XM_017016195.2:c.560C>G, XM_017016195.2:c.560C>A, XM_017016195.1:c.560C>T, XM_017016195.1:c.560C>G, XM_017016195.1:c.560C>A, XM_017016198.2:c.365C>T, XM_017016198.2:c.365C>G, XM_017016198.2:c.365C>A, XM_017016198.1:c.365C>T, XM_017016198.1:c.365C>G, XM_017016198.1:c.365C>A, NM_001243539.2:c.278C>T, NM_001243539.2:c.278C>G, NM_001243539.2:c.278C>A, NM_001243539.1:c.278C>T, NM_001243539.1:c.278C>G, NM_001243539.1:c.278C>A, NM_001351097.2:c.179C>T, NM_001351097.2:c.179C>G, NM_001351097.2:c.179C>A, NM_001351097.1:c.179C>T, NM_001351097.1:c.179C>G, NM_001351097.1:c.179C>A, XM_011519468.2:c.713C>T, XM_011519468.2:c.713C>G, XM_011519468.2:c.713C>A, XM_011519468.1:c.713C>T, XM_011519468.1:c.713C>G, XM_011519468.1:c.713C>A, NR_046362.2:n.274C>T, NR_046362.2:n.274C>G, NR_046362.2:n.274C>A, NR_046362.1:n.415C>T, NR_046362.1:n.415C>G, NR_046362.1:n.415C>A, XM_047425182.1:c.614C>T, XM_047425182.1:c.614C>G, XM_047425182.1:c.614C>A, XM_047425184.1:c.560C>T, XM_047425184.1:c.560C>G, XM_047425184.1:c.560C>A, XM_047425181.1:c.644C>T, XM_047425181.1:c.644C>G, XM_047425181.1:c.644C>A, NR_033494.1:n.701C>T, NR_033494.1:n.701C>G, NR_033494.1:n.701C>A, XM_047425185.1:c.278C>T, XM_047425185.1:c.278C>G, XM_047425185.1:c.278C>A, NM_001351096.1:c.278C>T, NM_001351096.1:c.278C>G, NM_001351096.1:c.278C>A, XM_047425191.1:c.266C>T, XM_047425191.1:c.266C>G, XM_047425191.1:c.266C>A, NM_001256765.1:c.644C>T, NM_001256765.1:c.644C>G, NM_001256765.1:c.644C>A, XM_047425186.1:c.491C>T, XM_047425186.1:c.491C>G, XM_047425186.1:c.491C>A, XM_047425183.1:c.545C>T, XM_047425183.1:c.545C>G, XM_047425183.1:c.545C>A, XM_047425187.1:c.392C>T, XM_047425187.1:c.392C>G, XM_047425187.1:c.392C>A, XM_047425190.1:c.296C>T, XM_047425190.1:c.296C>G, XM_047425190.1:c.296C>A, XM_047425189.1:c.296C>T, XM_047425189.1:c.296C>G, XM_047425189.1:c.296C>A, XM_047425188.1:c.392C>T, XM_047425188.1:c.392C>G, XM_047425188.1:c.392C>A, NP_002180.1:p.Pro129Leu, NP_002180.1:p.Pro129Arg, NP_002180.1:p.Pro129His, XP_011517768.1:p.Pro238Leu, XP_011517768.1:p.Pro238Arg, XP_011517768.1:p.Pro238His, XP_011517763.1:p.Pro238Leu, XP_011517763.1:p.Pro238Arg, XP_011517763.1:p.Pro238His, XP_011517765.1:p.Pro205Leu, XP_011517765.1:p.Pro205Arg, XP_011517765.1:p.Pro205His, XP_011517766.1:p.Pro187Leu, XP_011517766.1:p.Pro187Arg, XP_011517766.1:p.Pro187His, XP_011517779.1:p.Pro66Leu, XP_011517779.1:p.Pro66Arg, XP_011517779.1:p.Pro66His, NP_751950.2:p.Pro96Leu, NP_751950.2:p.Pro96Arg, NP_751950.2:p.Pro96His, XP_011517778.1:p.Pro66Leu, XP_011517778.1:p.Pro66Arg, XP_011517778.1:p.Pro66His, XP_011517773.1:p.Pro122Leu, XP_011517773.1:p.Pro122Arg, XP_011517773.1:p.Pro122His, XP_011517764.1:p.Pro215Leu, XP_011517764.1:p.Pro215Arg, XP_011517764.1:p.Pro215His, XP_016871686.1:p.Pro93Leu, XP_016871686.1:p.Pro93Arg, XP_016871686.1:p.Pro93His, XP_011517776.1:p.Pro89Leu, XP_011517776.1:p.Pro89Arg, XP_011517776.1:p.Pro89His, XP_011517769.1:p.Pro164Leu, XP_011517769.1:p.Pro164Arg, XP_011517769.1:p.Pro164His, XP_011517772.1:p.Pro131Leu, XP_011517772.1:p.Pro131Arg, XP_011517772.1:p.Pro131His, XP_011517774.1:p.Pro99Leu, XP_011517774.1:p.Pro99Arg, XP_011517774.1:p.Pro99His, XP_011517777.1:p.Pro66Leu, XP_011517777.1:p.Pro66Arg, XP_011517777.1:p.Pro66His, XP_011517767.1:p.Pro238Leu, XP_011517767.1:p.Pro238Arg, XP_011517767.1:p.Pro238His, XP_011517771.1:p.Pro205Leu, XP_011517771.1:p.Pro205Arg, XP_011517771.1:p.Pro205His, NP_001338024.1:p.Pro154Leu, NP_001338024.1:p.Pro154Arg, NP_001338024.1:p.Pro154His, XP_016871684.1:p.Pro187Leu, XP_016871684.1:p.Pro187Arg, XP_016871684.1:p.Pro187His, XP_016871687.1:p.Pro122Leu, XP_016871687.1:p.Pro122Arg, XP_016871687.1:p.Pro122His, NP_001230468.1:p.Pro93Leu, NP_001230468.1:p.Pro93Arg, NP_001230468.1:p.Pro93His, NP_001338026.1:p.Pro60Leu, NP_001338026.1:p.Pro60Arg, NP_001338026.1:p.Pro60His, XP_011517770.1:p.Pro238Leu, XP_011517770.1:p.Pro238Arg, XP_011517770.1:p.Pro238His, XP_047281138.1:p.Pro205Leu, XP_047281138.1:p.Pro205Arg, XP_047281138.1:p.Pro205His, XP_047281140.1:p.Pro187Leu, XP_047281140.1:p.Pro187Arg, XP_047281140.1:p.Pro187His, XP_047281137.1:p.Pro215Leu, XP_047281137.1:p.Pro215Arg, XP_047281137.1:p.Pro215His, XP_047281141.1:p.Pro93Leu, XP_047281141.1:p.Pro93Arg, XP_047281141.1:p.Pro93His, NP_001338025.1:p.Pro93Leu, NP_001338025.1:p.Pro93Arg, NP_001338025.1:p.Pro93His, XP_047281147.1:p.Pro89Leu, XP_047281147.1:p.Pro89Arg, XP_047281147.1:p.Pro89His, NP_001243694.1:p.Pro215Leu, NP_001243694.1:p.Pro215Arg, NP_001243694.1:p.Pro215His, XP_047281142.1:p.Pro164Leu, XP_047281142.1:p.Pro164Arg, XP_047281142.1:p.Pro164His, XP_047281139.1:p.Pro182Leu, XP_047281139.1:p.Pro182Arg, XP_047281139.1:p.Pro182His, XP_047281143.1:p.Pro131Leu, XP_047281143.1:p.Pro131Arg, XP_047281143.1:p.Pro131His, XP_047281146.1:p.Pro99Leu, XP_047281146.1:p.Pro99Arg, XP_047281146.1:p.Pro99His, XP_047281145.1:p.Pro99Leu, XP_047281145.1:p.Pro99Arg, XP_047281145.1:p.Pro99His, XP_047281144.1:p.Pro131Leu, XP_047281144.1:p.Pro131Arg, XP_047281144.1:p.Pro131His

                          13.

                          rs1467582814 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            C>A [Show Flanks]
                            Chromosome:
                            10:5949032 (GRCh38)
                            10:5990995 (GRCh37)
                            Canonical SPDI:
                            NC_000010.11:5949031:C:A
                            Gene:
                            IL15RA (Varview)
                            Functional Consequence:
                            coding_sequence_variant,3_prime_UTR_variant,stop_gained,downstream_transcript_variant,genic_downstream_transcript_variant
                            Validated:
                            by frequency,by alfa
                            MAF:
                            A=0./0 (ALFA)
                            A=0.000004/1 (TOPMED)
                            HGVS:
                            NC_000010.11:g.5949032C>A, NC_000010.10:g.5990995C>A, XM_011519461.3:c.1228G>T, XM_011519461.2:c.1228G>T, XM_011519461.1:c.1228G>T, XM_011519463.3:c.1129G>T, XM_011519463.2:c.1129G>T, XM_011519463.1:c.1129G>T, XM_011519464.3:c.1075G>T, XM_011519464.2:c.1075G>T, XM_011519464.1:c.1075G>T, XM_011519471.3:c.880G>T, XM_011519471.2:c.880G>T, XM_011519471.1:c.880G>T, XM_011519462.3:c.1159G>T, XM_011519462.2:c.1159G>T, XM_011519462.1:c.1159G>T, XM_017016197.3:c.793G>T, XM_017016197.2:c.793G>T, XM_017016197.1:c.793G>T, XM_011519474.3:c.781G>T, XM_011519474.2:c.781G>T, XM_011519474.1:c.781G>T, XM_011519467.3:c.1006G>T, XM_011519467.2:c.1006G>T, XM_011519467.1:c.1006G>T, XM_011519470.3:c.907G>T, XM_011519470.2:c.907G>T, XM_011519470.1:c.907G>T, XM_011519472.3:c.811G>T, XM_011519472.2:c.811G>T, XM_011519472.1:c.811G>T, XM_011519475.3:c.712G>T, XM_011519475.2:c.712G>T, XM_011519475.1:c.712G>T, XM_047425185.1:c.793G>T, XM_047425188.1:c.*258G>T, XP_011517763.1:p.Glu410Ter, XP_011517765.1:p.Glu377Ter, XP_011517766.1:p.Glu359Ter, XP_011517773.1:p.Glu294Ter, XP_011517764.1:p.Glu387Ter, XP_016871686.1:p.Glu265Ter, XP_011517776.1:p.Glu261Ter, XP_011517769.1:p.Glu336Ter, XP_011517772.1:p.Glu303Ter, XP_011517774.1:p.Glu271Ter, XP_011517777.1:p.Glu238Ter, XP_047281141.1:p.Glu265Ter

                            14.

                            rs1466875044 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              G>A [Show Flanks]
                              Chromosome:
                              10:5948966 (GRCh38)
                              10:5990929 (GRCh37)
                              Canonical SPDI:
                              NC_000010.11:5948965:G:A
                              Gene:
                              IL15RA (Varview)
                              Functional Consequence:
                              coding_sequence_variant,3_prime_UTR_variant,downstream_transcript_variant,genic_downstream_transcript_variant,missense_variant
                              Validated:
                              by frequency
                              MAF:
                              A=0.00002/1 (GnomAD_exomes)
                              HGVS:
                              NC_000010.11:g.5948966G>A, NC_000010.10:g.5990929G>A, XM_011519461.3:c.1294C>T, XM_011519461.2:c.1294C>T, XM_011519461.1:c.1294C>T, XM_011519463.3:c.1195C>T, XM_011519463.2:c.1195C>T, XM_011519463.1:c.1195C>T, XM_011519464.3:c.1141C>T, XM_011519464.2:c.1141C>T, XM_011519464.1:c.1141C>T, XM_011519471.3:c.946C>T, XM_011519471.2:c.946C>T, XM_011519471.1:c.946C>T, XM_011519462.3:c.1225C>T, XM_011519462.2:c.1225C>T, XM_011519462.1:c.1225C>T, XM_017016197.3:c.859C>T, XM_017016197.2:c.859C>T, XM_017016197.1:c.859C>T, XM_011519474.3:c.847C>T, XM_011519474.2:c.847C>T, XM_011519474.1:c.847C>T, XM_011519467.3:c.1072C>T, XM_011519467.2:c.1072C>T, XM_011519467.1:c.1072C>T, XM_011519470.3:c.973C>T, XM_011519470.2:c.973C>T, XM_011519470.1:c.973C>T, XM_011519472.3:c.877C>T, XM_011519472.2:c.877C>T, XM_011519472.1:c.877C>T, XM_011519475.3:c.778C>T, XM_011519475.2:c.778C>T, XM_011519475.1:c.778C>T, XM_047425185.1:c.859C>T, XM_047425188.1:c.*324C>T, XP_011517763.1:p.His432Tyr, XP_011517765.1:p.His399Tyr, XP_011517766.1:p.His381Tyr, XP_011517773.1:p.His316Tyr, XP_011517764.1:p.His409Tyr, XP_016871686.1:p.His287Tyr, XP_011517776.1:p.His283Tyr, XP_011517769.1:p.His358Tyr, XP_011517772.1:p.His325Tyr, XP_011517774.1:p.His293Tyr, XP_011517777.1:p.His260Tyr, XP_047281141.1:p.His287Tyr

                              15.

                              rs1466689108 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                A>G [Show Flanks]
                                Chromosome:
                                10:5956405 (GRCh38)
                                10:5998368 (GRCh37)
                                Canonical SPDI:
                                NC_000010.11:5956404:A:G
                                Gene:
                                IL15RA (Varview)
                                Functional Consequence:
                                coding_sequence_variant,synonymous_variant,non_coding_transcript_variant,genic_downstream_transcript_variant
                                Validated:
                                by frequency
                                MAF:
                                G=0.000004/1 (GnomAD_exomes)
                                HGVS:
                                NC_000010.11:g.5956405A>G, NC_000010.10:g.5998368A>G, NM_002189.4:c.666T>C, NM_002189.3:c.666T>C, XM_011519466.3:c.993T>C, XM_011519466.2:c.993T>C, XM_011519466.1:c.993T>C, XM_011519461.3:c.993T>C, XM_011519461.2:c.993T>C, XM_011519461.1:c.993T>C, XM_011519463.3:c.894T>C, XM_011519463.2:c.894T>C, XM_011519463.1:c.894T>C, XM_011519464.3:c.840T>C, XM_011519464.2:c.840T>C, XM_011519464.1:c.840T>C, XM_011519477.3:c.477T>C, XM_011519477.2:c.477T>C, XM_011519477.1:c.477T>C, NM_172200.3:c.567T>C, NM_172200.2:c.567T>C, XM_011519476.3:c.477T>C, XM_011519476.2:c.477T>C, XM_011519476.1:c.477T>C, XM_011519471.3:c.645T>C, XM_011519471.2:c.645T>C, XM_011519471.1:c.645T>C, XM_011519462.3:c.924T>C, XM_011519462.2:c.924T>C, XM_011519462.1:c.924T>C, XM_017016197.3:c.558T>C, XM_017016197.2:c.558T>C, XM_017016197.1:c.558T>C, XM_011519474.3:c.546T>C, XM_011519474.2:c.546T>C, XM_011519474.1:c.546T>C, XM_011519467.3:c.771T>C, XM_011519467.2:c.771T>C, XM_011519467.1:c.771T>C, XM_011519470.3:c.672T>C, XM_011519470.2:c.672T>C, XM_011519470.1:c.672T>C, XM_011519472.3:c.576T>C, XM_011519472.2:c.576T>C, XM_011519472.1:c.576T>C, XM_011519475.3:c.477T>C, XM_011519475.2:c.477T>C, XM_011519475.1:c.477T>C, XM_011519465.2:c.993T>C, XM_011519465.1:c.993T>C, XM_011519469.2:c.894T>C, XM_011519469.1:c.894T>C, NM_001351095.2:c.741T>C, NM_001351095.1:c.741T>C, XM_017016195.2:c.840T>C, XM_017016195.1:c.840T>C, XM_017016198.2:c.645T>C, XM_017016198.1:c.645T>C, NM_001243539.2:c.558T>C, NM_001243539.1:c.558T>C, NM_001351097.2:c.459T>C, NM_001351097.1:c.459T>C, XM_011519468.2:c.993T>C, XM_011519468.1:c.993T>C, NR_046362.2:n.554T>C, NR_046362.1:n.695T>C, XM_047425182.1:c.894T>C, XM_047425184.1:c.840T>C, XM_047425181.1:c.924T>C, NR_033494.1:n.981T>C, XM_047425185.1:c.558T>C, NM_001351096.1:c.558T>C, XM_047425191.1:c.546T>C, NM_001256765.1:c.924T>C, XM_047425186.1:c.771T>C, XM_047425183.1:c.825T>C, XM_047425187.1:c.672T>C, XM_047425190.1:c.576T>C, XM_047425189.1:c.576T>C, XM_047425188.1:c.672T>C

                                16.

                                rs1464872814 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  G>C [Show Flanks]
                                  Chromosome:
                                  10:5949210 (GRCh38)
                                  10:5991173 (GRCh37)
                                  Canonical SPDI:
                                  NC_000010.11:5949209:G:C
                                  Gene:
                                  IL15RA (Varview)
                                  Functional Consequence:
                                  coding_sequence_variant,3_prime_UTR_variant,synonymous_variant,genic_downstream_transcript_variant
                                  Validated:
                                  by frequency
                                  MAF:
                                  C=0.000007/1 (GnomAD_exomes)
                                  HGVS:
                                  NC_000010.11:g.5949210G>C, NC_000010.10:g.5991173G>C, XM_011519461.3:c.1050C>G, XM_011519461.2:c.1050C>G, XM_011519461.1:c.1050C>G, XM_011519463.3:c.951C>G, XM_011519463.2:c.951C>G, XM_011519463.1:c.951C>G, XM_011519464.3:c.897C>G, XM_011519464.2:c.897C>G, XM_011519464.1:c.897C>G, XM_011519471.3:c.702C>G, XM_011519471.2:c.702C>G, XM_011519471.1:c.702C>G, XM_011519462.3:c.981C>G, XM_011519462.2:c.981C>G, XM_011519462.1:c.981C>G, XM_017016197.3:c.615C>G, XM_017016197.2:c.615C>G, XM_017016197.1:c.615C>G, XM_011519474.3:c.603C>G, XM_011519474.2:c.603C>G, XM_011519474.1:c.603C>G, XM_011519467.3:c.828C>G, XM_011519467.2:c.828C>G, XM_011519467.1:c.828C>G, XM_011519470.3:c.729C>G, XM_011519470.2:c.729C>G, XM_011519470.1:c.729C>G, XM_011519472.3:c.633C>G, XM_011519472.2:c.633C>G, XM_011519472.1:c.633C>G, XM_011519475.3:c.534C>G, XM_011519475.2:c.534C>G, XM_011519475.1:c.534C>G, XM_011519468.2:c.*80C>G, XM_011519468.1:c.*80C>G, XM_047425185.1:c.615C>G, XM_047425188.1:c.*80C>G

                                  17.

                                  rs1462905816 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    T>C [Show Flanks]
                                    Chromosome:
                                    10:5949175 (GRCh38)
                                    10:5991138 (GRCh37)
                                    Canonical SPDI:
                                    NC_000010.11:5949174:T:C
                                    Gene:
                                    IL15RA (Varview)
                                    Functional Consequence:
                                    coding_sequence_variant,3_prime_UTR_variant,genic_downstream_transcript_variant,missense_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_000010.11:g.5949175T>C, NC_000010.10:g.5991138T>C, XM_011519461.3:c.1085A>G, XM_011519461.2:c.1085A>G, XM_011519461.1:c.1085A>G, XM_011519463.3:c.986A>G, XM_011519463.2:c.986A>G, XM_011519463.1:c.986A>G, XM_011519464.3:c.932A>G, XM_011519464.2:c.932A>G, XM_011519464.1:c.932A>G, XM_011519471.3:c.737A>G, XM_011519471.2:c.737A>G, XM_011519471.1:c.737A>G, XM_011519462.3:c.1016A>G, XM_011519462.2:c.1016A>G, XM_011519462.1:c.1016A>G, XM_017016197.3:c.650A>G, XM_017016197.2:c.650A>G, XM_017016197.1:c.650A>G, XM_011519474.3:c.638A>G, XM_011519474.2:c.638A>G, XM_011519474.1:c.638A>G, XM_011519467.3:c.863A>G, XM_011519467.2:c.863A>G, XM_011519467.1:c.863A>G, XM_011519470.3:c.764A>G, XM_011519470.2:c.764A>G, XM_011519470.1:c.764A>G, XM_011519472.3:c.668A>G, XM_011519472.2:c.668A>G, XM_011519472.1:c.668A>G, XM_011519475.3:c.569A>G, XM_011519475.2:c.569A>G, XM_011519475.1:c.569A>G, XM_011519468.2:c.*115A>G, XM_011519468.1:c.*115A>G, XM_047425185.1:c.650A>G, XM_047425188.1:c.*115A>G, XP_011517763.1:p.Asp362Gly, XP_011517765.1:p.Asp329Gly, XP_011517766.1:p.Asp311Gly, XP_011517773.1:p.Asp246Gly, XP_011517764.1:p.Asp339Gly, XP_016871686.1:p.Asp217Gly, XP_011517776.1:p.Asp213Gly, XP_011517769.1:p.Asp288Gly, XP_011517772.1:p.Asp255Gly, XP_011517774.1:p.Asp223Gly, XP_011517777.1:p.Asp190Gly, XP_047281141.1:p.Asp217Gly

                                    18.

                                    rs1461608801 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      G>C [Show Flanks]
                                      Chromosome:
                                      10:5949056 (GRCh38)
                                      10:5991019 (GRCh37)
                                      Canonical SPDI:
                                      NC_000010.11:5949055:G:C
                                      Gene:
                                      IL15RA (Varview)
                                      Functional Consequence:
                                      coding_sequence_variant,3_prime_UTR_variant,downstream_transcript_variant,genic_downstream_transcript_variant,missense_variant
                                      Validated:
                                      by frequency
                                      MAF:
                                      C=0.00002/1 (GnomAD_exomes)
                                      HGVS:
                                      NC_000010.11:g.5949056G>C, NC_000010.10:g.5991019G>C, XM_011519461.3:c.1204C>G, XM_011519461.2:c.1204C>G, XM_011519461.1:c.1204C>G, XM_011519463.3:c.1105C>G, XM_011519463.2:c.1105C>G, XM_011519463.1:c.1105C>G, XM_011519464.3:c.1051C>G, XM_011519464.2:c.1051C>G, XM_011519464.1:c.1051C>G, XM_011519471.3:c.856C>G, XM_011519471.2:c.856C>G, XM_011519471.1:c.856C>G, XM_011519462.3:c.1135C>G, XM_011519462.2:c.1135C>G, XM_011519462.1:c.1135C>G, XM_017016197.3:c.769C>G, XM_017016197.2:c.769C>G, XM_017016197.1:c.769C>G, XM_011519474.3:c.757C>G, XM_011519474.2:c.757C>G, XM_011519474.1:c.757C>G, XM_011519467.3:c.982C>G, XM_011519467.2:c.982C>G, XM_011519467.1:c.982C>G, XM_011519470.3:c.883C>G, XM_011519470.2:c.883C>G, XM_011519470.1:c.883C>G, XM_011519472.3:c.787C>G, XM_011519472.2:c.787C>G, XM_011519472.1:c.787C>G, XM_011519475.3:c.688C>G, XM_011519475.2:c.688C>G, XM_011519475.1:c.688C>G, XM_047425185.1:c.769C>G, XM_047425188.1:c.*234C>G, XP_011517763.1:p.Leu402Val, XP_011517765.1:p.Leu369Val, XP_011517766.1:p.Leu351Val, XP_011517773.1:p.Leu286Val, XP_011517764.1:p.Leu379Val, XP_016871686.1:p.Leu257Val, XP_011517776.1:p.Leu253Val, XP_011517769.1:p.Leu328Val, XP_011517772.1:p.Leu295Val, XP_011517774.1:p.Leu263Val, XP_011517777.1:p.Leu230Val, XP_047281141.1:p.Leu257Val

                                      19.

                                      rs1459858633 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        A>G [Show Flanks]
                                        Chromosome:
                                        10:5966180 (GRCh38)
                                        10:6008143 (GRCh37)
                                        Canonical SPDI:
                                        NC_000010.11:5966179:A:G
                                        Gene:
                                        IL15RA (Varview), LOC107984200 (Varview)
                                        Functional Consequence:
                                        coding_sequence_variant,intron_variant,missense_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        G=0.000071/1 (ALFA)
                                        G=0.000004/1 (TOPMED)
                                        HGVS:
                                        NC_000010.11:g.5966180A>G, NC_000010.10:g.6008143A>G, NM_002189.4:c.248T>C, NM_002189.3:c.248T>C, XM_011519466.3:c.575T>C, XM_011519466.2:c.575T>C, XM_011519466.1:c.575T>C, XM_011519461.3:c.575T>C, XM_011519461.2:c.575T>C, XM_011519461.1:c.575T>C, XM_011519463.3:c.575T>C, XM_011519463.2:c.575T>C, XM_011519463.1:c.575T>C, XM_011519464.3:c.422T>C, XM_011519464.2:c.422T>C, XM_011519464.1:c.422T>C, NM_172200.3:c.248T>C, NM_172200.2:c.248T>C, XM_011519462.3:c.506T>C, XM_011519462.2:c.506T>C, XM_011519462.1:c.506T>C, XM_017016197.3:c.140T>C, XM_017016197.2:c.140T>C, XM_017016197.1:c.140T>C, XM_011519467.3:c.353T>C, XM_011519467.2:c.353T>C, XM_011519467.1:c.353T>C, XM_011519470.3:c.353T>C, XM_011519470.2:c.353T>C, XM_011519470.1:c.353T>C, XM_011519465.2:c.575T>C, XM_011519465.1:c.575T>C, XM_011519469.2:c.575T>C, XM_011519469.1:c.575T>C, NM_001351095.2:c.422T>C, NM_001351095.1:c.422T>C, XM_017016195.2:c.422T>C, XM_017016195.1:c.422T>C, NM_001243539.2:c.140T>C, NM_001243539.1:c.140T>C, NM_001351097.2:c.140T>C, NM_001351097.1:c.140T>C, XM_011519468.2:c.575T>C, XM_011519468.1:c.575T>C, XM_017016199.2:c.575T>C, XM_017016199.1:c.575T>C, XM_047425182.1:c.575T>C, XM_047425184.1:c.422T>C, XM_047425181.1:c.506T>C, NR_033494.1:n.563T>C, XM_047425185.1:c.140T>C, NM_001351096.1:c.140T>C, NM_001256765.1:c.506T>C, XM_047425186.1:c.353T>C, XM_047425183.1:c.506T>C, XM_047425187.1:c.353T>C, XM_047425188.1:c.353T>C, NP_002180.1:p.Val83Ala, XP_011517768.1:p.Val192Ala, XP_011517763.1:p.Val192Ala, XP_011517765.1:p.Val192Ala, XP_011517766.1:p.Val141Ala, NP_751950.2:p.Val83Ala, XP_011517764.1:p.Val169Ala, XP_016871686.1:p.Val47Ala, XP_011517769.1:p.Val118Ala, XP_011517772.1:p.Val118Ala, XP_011517767.1:p.Val192Ala, XP_011517771.1:p.Val192Ala, NP_001338024.1:p.Val141Ala, XP_016871684.1:p.Val141Ala, NP_001230468.1:p.Val47Ala, NP_001338026.1:p.Val47Ala, XP_011517770.1:p.Val192Ala, XP_016871688.1:p.Val192Ala, XP_047281138.1:p.Val192Ala, XP_047281140.1:p.Val141Ala, XP_047281137.1:p.Val169Ala, XP_047281141.1:p.Val47Ala, NP_001338025.1:p.Val47Ala, NP_001243694.1:p.Val169Ala, XP_047281142.1:p.Val118Ala, XP_047281139.1:p.Val169Ala, XP_047281143.1:p.Val118Ala, XP_047281144.1:p.Val118Ala

                                        20.

                                        rs1458407732 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          C>T [Show Flanks]
                                          Chromosome:
                                          10:5966236 (GRCh38)
                                          10:6008199 (GRCh37)
                                          Canonical SPDI:
                                          NC_000010.11:5966235:C:T
                                          Gene:
                                          IL15RA (Varview), LOC107984200 (Varview)
                                          Functional Consequence:
                                          coding_sequence_variant,synonymous_variant,intron_variant
                                          Validated:
                                          by frequency,by alfa
                                          MAF:
                                          T=0.000071/1 (ALFA)
                                          T=0.000004/1 (TOPMED)
                                          HGVS:
                                          NC_000010.11:g.5966236C>T, NC_000010.10:g.6008199C>T, NM_002189.4:c.192G>A, NM_002189.3:c.192G>A, XM_011519466.3:c.519G>A, XM_011519466.2:c.519G>A, XM_011519466.1:c.519G>A, XM_011519461.3:c.519G>A, XM_011519461.2:c.519G>A, XM_011519461.1:c.519G>A, XM_011519463.3:c.519G>A, XM_011519463.2:c.519G>A, XM_011519463.1:c.519G>A, XM_011519464.3:c.366G>A, XM_011519464.2:c.366G>A, XM_011519464.1:c.366G>A, NM_172200.3:c.192G>A, NM_172200.2:c.192G>A, XM_011519462.3:c.450G>A, XM_011519462.2:c.450G>A, XM_011519462.1:c.450G>A, XM_017016197.3:c.84G>A, XM_017016197.2:c.84G>A, XM_017016197.1:c.84G>A, XM_011519467.3:c.297G>A, XM_011519467.2:c.297G>A, XM_011519467.1:c.297G>A, XM_011519470.3:c.297G>A, XM_011519470.2:c.297G>A, XM_011519470.1:c.297G>A, XM_011519465.2:c.519G>A, XM_011519465.1:c.519G>A, XM_011519469.2:c.519G>A, XM_011519469.1:c.519G>A, NM_001351095.2:c.366G>A, NM_001351095.1:c.366G>A, XM_017016195.2:c.366G>A, XM_017016195.1:c.366G>A, NM_001243539.2:c.84G>A, NM_001243539.1:c.84G>A, NM_001351097.2:c.84G>A, NM_001351097.1:c.84G>A, XM_011519468.2:c.519G>A, XM_011519468.1:c.519G>A, XM_017016199.2:c.519G>A, XM_017016199.1:c.519G>A, XM_047425182.1:c.519G>A, XM_047425184.1:c.366G>A, XM_047425181.1:c.450G>A, NR_033494.1:n.507G>A, XM_047425185.1:c.84G>A, NM_001351096.1:c.84G>A, NM_001256765.1:c.450G>A, XM_047425186.1:c.297G>A, XM_047425183.1:c.450G>A, XM_047425187.1:c.297G>A, XM_047425188.1:c.297G>A

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