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Items: 1 to 20 of 371

1.

rs1490340872 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>A,C [Show Flanks]
    Chromosome:
    10:5977791 (GRCh38)
    10:6019754 (GRCh37)
    Canonical SPDI:
    NC_000010.11:5977790:G:A,NC_000010.11:5977790:G:C
    Gene:
    IL15RA (Varview)
    Functional Consequence:
    5_prime_UTR_variant,non_coding_transcript_variant,upstream_transcript_variant,missense_variant,coding_sequence_variant,genic_upstream_transcript_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    C=0./0 (ALFA)
    C=0.000019/5 (TOPMED)
    C=0.000029/4 (GnomAD)
    HGVS:
    NC_000010.11:g.5977791G>A, NC_000010.11:g.5977791G>C, NC_000010.10:g.6019754G>A, NC_000010.10:g.6019754G>C, XM_011519466.3:c.248C>T, XM_011519466.3:c.248C>G, XM_011519466.2:c.248C>T, XM_011519466.2:c.248C>G, XM_011519466.1:c.248C>T, XM_011519466.1:c.248C>G, XM_011519461.3:c.248C>T, XM_011519461.3:c.248C>G, XM_011519461.2:c.248C>T, XM_011519461.2:c.248C>G, XM_011519461.1:c.248C>T, XM_011519461.1:c.248C>G, XM_011519463.3:c.248C>T, XM_011519463.3:c.248C>G, XM_011519463.2:c.248C>T, XM_011519463.2:c.248C>G, XM_011519463.1:c.248C>T, XM_011519463.1:c.248C>G, XM_011519464.3:c.248C>T, XM_011519464.3:c.248C>G, XM_011519464.2:c.248C>T, XM_011519464.2:c.248C>G, XM_011519464.1:c.248C>T, XM_011519464.1:c.248C>G, XM_011519471.3:c.248C>T, XM_011519471.3:c.248C>G, XM_011519471.2:c.248C>T, XM_011519471.2:c.248C>G, XM_011519471.1:c.248C>T, XM_011519471.1:c.248C>G, XM_011519474.3:c.248C>T, XM_011519474.3:c.248C>G, XM_011519474.2:c.248C>T, XM_011519474.2:c.248C>G, XM_011519474.1:c.248C>T, XM_011519474.1:c.248C>G, XM_011519465.2:c.248C>T, XM_011519465.2:c.248C>G, XM_011519465.1:c.248C>T, XM_011519465.1:c.248C>G, XM_011519469.2:c.248C>T, XM_011519469.2:c.248C>G, XM_011519469.1:c.248C>T, XM_011519469.1:c.248C>G, NM_001351095.2:c.248C>T, NM_001351095.2:c.248C>G, NM_001351095.1:c.248C>T, NM_001351095.1:c.248C>G, XM_017016195.2:c.248C>T, XM_017016195.2:c.248C>G, XM_017016195.1:c.248C>T, XM_017016195.1:c.248C>G, XM_017016198.2:c.248C>T, XM_017016198.2:c.248C>G, XM_017016198.1:c.248C>T, XM_017016198.1:c.248C>G, NM_001243539.2:c.-35C>T, NM_001243539.2:c.-35C>G, NM_001243539.1:c.-35C>T, NM_001243539.1:c.-35C>G, NM_001351097.2:c.-35C>T, NM_001351097.2:c.-35C>G, NM_001351097.1:c.-35C>T, NM_001351097.1:c.-35C>G, XM_011519468.2:c.248C>T, XM_011519468.2:c.248C>G, XM_011519468.1:c.248C>T, XM_011519468.1:c.248C>G, NR_046362.2:n.256C>T, NR_046362.2:n.256C>G, NR_046362.1:n.397C>T, NR_046362.1:n.397C>G, XM_017016199.2:c.248C>T, XM_017016199.2:c.248C>G, XM_017016199.1:c.248C>T, XM_017016199.1:c.248C>G, XM_047425182.1:c.248C>T, XM_047425182.1:c.248C>G, XM_047425184.1:c.248C>T, XM_047425184.1:c.248C>G, NR_033494.1:n.389C>T, NR_033494.1:n.389C>G, XM_047425185.1:c.-35C>T, XM_047425185.1:c.-35C>G, XM_047425191.1:c.248C>T, XM_047425191.1:c.248C>G, XP_011517768.1:p.Ser83Phe, XP_011517768.1:p.Ser83Cys, XP_011517763.1:p.Ser83Phe, XP_011517763.1:p.Ser83Cys, XP_011517765.1:p.Ser83Phe, XP_011517765.1:p.Ser83Cys, XP_011517766.1:p.Ser83Phe, XP_011517766.1:p.Ser83Cys, XP_011517773.1:p.Ser83Phe, XP_011517773.1:p.Ser83Cys, XP_011517776.1:p.Ser83Phe, XP_011517776.1:p.Ser83Cys, XP_011517767.1:p.Ser83Phe, XP_011517767.1:p.Ser83Cys, XP_011517771.1:p.Ser83Phe, XP_011517771.1:p.Ser83Cys, NP_001338024.1:p.Ser83Phe, NP_001338024.1:p.Ser83Cys, XP_016871684.1:p.Ser83Phe, XP_016871684.1:p.Ser83Cys, XP_016871687.1:p.Ser83Phe, XP_016871687.1:p.Ser83Cys, XP_011517770.1:p.Ser83Phe, XP_011517770.1:p.Ser83Cys, XP_016871688.1:p.Ser83Phe, XP_016871688.1:p.Ser83Cys, XP_047281138.1:p.Ser83Phe, XP_047281138.1:p.Ser83Cys, XP_047281140.1:p.Ser83Phe, XP_047281140.1:p.Ser83Cys, XP_047281147.1:p.Ser83Phe, XP_047281147.1:p.Ser83Cys

    2.

    rs1486847170 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      G>C [Show Flanks]
      Chromosome:
      10:5978273 (GRCh38)
      10:6020236 (GRCh37)
      Canonical SPDI:
      NC_000010.11:5978272:G:C
      Gene:
      IL15RA (Varview)
      Functional Consequence:
      5_prime_UTR_variant,genic_upstream_transcript_variant,stop_gained,coding_sequence_variant,upstream_transcript_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      C=0./0 (ALFA)
      C=0.000015/4 (TOPMED)
      C=0.000021/3 (GnomAD)
      HGVS:
      NC_000010.11:g.5978273G>C, NC_000010.10:g.6020236G>C, XM_011519466.3:c.176C>G, XM_011519466.2:c.176C>G, XM_011519466.1:c.176C>G, XM_011519461.3:c.176C>G, XM_011519461.2:c.176C>G, XM_011519461.1:c.176C>G, XM_011519463.3:c.176C>G, XM_011519463.2:c.176C>G, XM_011519463.1:c.176C>G, XM_011519464.3:c.176C>G, XM_011519464.2:c.176C>G, XM_011519464.1:c.176C>G, XM_011519471.3:c.176C>G, XM_011519471.2:c.176C>G, XM_011519471.1:c.176C>G, XM_011519474.3:c.176C>G, XM_011519474.2:c.176C>G, XM_011519474.1:c.176C>G, XM_011519465.2:c.176C>G, XM_011519465.1:c.176C>G, XM_011519469.2:c.176C>G, XM_011519469.1:c.176C>G, NM_001351095.2:c.176C>G, NM_001351095.1:c.176C>G, XM_017016195.2:c.176C>G, XM_017016195.1:c.176C>G, XM_017016198.2:c.176C>G, XM_017016198.1:c.176C>G, XM_011519468.2:c.176C>G, XM_011519468.1:c.176C>G, XM_017016199.2:c.176C>G, XM_017016199.1:c.176C>G, XM_047425182.1:c.176C>G, XM_047425184.1:c.176C>G, XM_047425185.1:c.-444C>G, XM_047425191.1:c.176C>G, XP_011517768.1:p.Ser59Ter, XP_011517763.1:p.Ser59Ter, XP_011517765.1:p.Ser59Ter, XP_011517766.1:p.Ser59Ter, XP_011517773.1:p.Ser59Ter, XP_011517776.1:p.Ser59Ter, XP_011517767.1:p.Ser59Ter, XP_011517771.1:p.Ser59Ter, NP_001338024.1:p.Ser59Ter, XP_016871684.1:p.Ser59Ter, XP_016871687.1:p.Ser59Ter, XP_011517770.1:p.Ser59Ter, XP_016871688.1:p.Ser59Ter, XP_047281138.1:p.Ser59Ter, XP_047281140.1:p.Ser59Ter, XP_047281147.1:p.Ser59Ter

      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.

        rs1483413906 [Homo sapiens]
          Variant type:
          DEL
          Alleles:
          T>- [Show Flanks]
          Chromosome:
          10:5953102 (GRCh38)
          10:5995065 (GRCh37)
          Canonical SPDI:
          NC_000010.11:5953101:T:
          Gene:
          IL15RA (Varview)
          Functional Consequence:
          3_prime_UTR_variant,intron_variant,non_coding_transcript_variant,genic_downstream_transcript_variant,coding_sequence_variant,frameshift_variant
          Validated:
          by frequency,by cluster
          MAF:
          -=0./0 (GnomAD)
          HGVS:
          NC_000010.11:g.5953102del, NC_000010.10:g.5995065del, NM_002189.4:c.797del, NM_002189.3:c.797del, XM_011519466.3:c.*158del, XM_011519466.2:c.*158del, XM_011519477.3:c.*158del, XM_011519477.2:c.*158del, NM_172200.3:c.698del, NM_172200.2:c.698del, XM_011519476.3:c.608del, XM_011519476.2:c.608del, XM_011519476.1:c.608del, XM_011519465.2:c.1124del, XM_011519465.1:c.1124del, XM_011519469.2:c.1025del, XM_011519469.1:c.1025del, NM_001351095.2:c.*158del, NM_001351095.1:c.*158del, XM_017016195.2:c.971del, XM_017016195.1:c.971del, XM_017016198.2:c.776del, XM_017016198.1:c.776del, NM_001243539.2:c.689del, NM_001243539.1:c.689del, NM_001351097.2:c.590del, NM_001351097.1:c.590del, NR_046362.2:n.685del, NR_046362.1:n.826del, XM_047425182.1:c.*158del, XM_047425184.1:c.*158del, XM_047425181.1:c.*158del, NR_033494.1:n.1112del, NM_001351096.1:c.*158del, XM_047425191.1:c.*158del, NM_001256765.1:c.1055del, XM_047425186.1:c.*158del, XM_047425183.1:c.956del, XM_047425187.1:c.*158del, XM_047425190.1:c.*158del, XM_047425189.1:c.707del, NP_002180.1:p.His266fs, NP_751950.2:p.His233fs, XP_011517778.1:p.His203fs, XP_011517767.1:p.His375fs, XP_011517771.1:p.His342fs, XP_016871684.1:p.His324fs, XP_016871687.1:p.His259fs, NP_001230468.1:p.His230fs, NP_001338026.1:p.His197fs, NP_001243694.1:p.His352fs, XP_047281139.1:p.His319fs, XP_047281145.1:p.His236fs

          5.

          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

            6.

            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

              7.

              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

                8.

                rs1477684487 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  T>A [Show Flanks]
                  Chromosome:
                  10:5953114 (GRCh38)
                  10:5995077 (GRCh37)
                  Canonical SPDI:
                  NC_000010.11:5953113:T:A
                  Gene:
                  IL15RA (Varview)
                  Functional Consequence:
                  3_prime_UTR_variant,intron_variant,non_coding_transcript_variant,missense_variant,genic_downstream_transcript_variant,coding_sequence_variant
                  Validated:
                  by frequency,by alfa
                  MAF:
                  A=0.000047/1 (ALFA)
                  A=0.000008/2 (GnomAD_exomes)
                  HGVS:
                  NC_000010.11:g.5953114T>A, NC_000010.10:g.5995077T>A, NM_002189.4:c.785A>T, NM_002189.3:c.785A>T, XM_011519466.3:c.*146A>T, XM_011519466.2:c.*146A>T, XM_011519466.1:c.*146A>T, XM_011519477.3:c.*146A>T, XM_011519477.2:c.*146A>T, XM_011519477.1:c.*146A>T, NM_172200.3:c.686A>T, NM_172200.2:c.686A>T, XM_011519476.3:c.596A>T, XM_011519476.2:c.596A>T, XM_011519476.1:c.596A>T, XM_011519465.2:c.1112A>T, XM_011519465.1:c.1112A>T, XM_011519469.2:c.1013A>T, XM_011519469.1:c.1013A>T, NM_001351095.2:c.*146A>T, NM_001351095.1:c.*146A>T, XM_017016195.2:c.959A>T, XM_017016195.1:c.959A>T, XM_017016198.2:c.764A>T, XM_017016198.1:c.764A>T, NM_001243539.2:c.677A>T, NM_001243539.1:c.677A>T, NM_001351097.2:c.578A>T, NM_001351097.1:c.578A>T, NR_046362.2:n.673A>T, NR_046362.1:n.814A>T, XM_047425182.1:c.*146A>T, XM_047425184.1:c.*146A>T, XM_047425181.1:c.*146A>T, NR_033494.1:n.1100A>T, NM_001351096.1:c.*146A>T, XM_047425191.1:c.*146A>T, NM_001256765.1:c.1043A>T, XM_047425186.1:c.*146A>T, XM_047425183.1:c.944A>T, XM_047425187.1:c.*146A>T, XM_047425190.1:c.*146A>T, XM_047425189.1:c.695A>T, NP_002180.1:p.Asn262Ile, NP_751950.2:p.Asn229Ile, XP_011517778.1:p.Asn199Ile, XP_011517767.1:p.Asn371Ile, XP_011517771.1:p.Asn338Ile, XP_016871684.1:p.Asn320Ile, XP_016871687.1:p.Asn255Ile, NP_001230468.1:p.Asn226Ile, NP_001338026.1:p.Asn193Ile, NP_001243694.1:p.Asn348Ile, XP_047281139.1:p.Asn315Ile, XP_047281145.1:p.Asn232Ile

                  9.

                  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

                    10.

                    rs1474205240 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      G>A [Show Flanks]
                      Chromosome:
                      10:5968891 (GRCh38)
                      10:6010854 (GRCh37)
                      Canonical SPDI:
                      NC_000010.11:5968890:G:A
                      Gene:
                      IL15RA (Varview), LOC107984200 (Varview)
                      Functional Consequence:
                      coding_sequence_variant,5_prime_UTR_variant,intron_variant,synonymous_variant
                      Validated:
                      by frequency
                      MAF:
                      A=0.000016/2 (GnomAD_exomes)
                      HGVS:

                      11.

                      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

                        12.

                        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

                          13.

                          rs1469096310 [Homo sapiens]
                            Variant type:
                            DELINS
                            Alleles:
                            T>- [Show Flanks]
                            Chromosome:
                            10:5968820 (GRCh38)
                            10:6010783 (GRCh37)
                            Canonical SPDI:
                            NC_000010.11:5968819:TTTT:TTT
                            Gene:
                            IL15RA (Varview), LOC107984200 (Varview)
                            Functional Consequence:
                            coding_sequence_variant,frameshift_variant,intron_variant,5_prime_UTR_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            TTT=0.000071/1 (ALFA)
                            -=0.000004/1 (TOPMED)
                            -=0.000008/1 (GnomAD_exomes)
                            HGVS:
                            NC_000010.11:g.5968823del, NC_000010.10:g.6010786del, XM_011519466.3:c.371del, XM_011519466.2:c.371del, XM_011519466.1:c.371del, XM_011519461.3:c.371del, XM_011519461.2:c.371del, XM_011519461.1:c.371del, XM_011519463.3:c.371del, XM_011519463.2:c.371del, XM_011519463.1:c.371del, XM_011519462.3:c.302del, XM_011519462.2:c.302del, XM_011519462.1:c.302del, XM_017016197.3:c.-175del, XM_017016197.2:c.-175del, XM_017016197.1:c.-175del, XM_011519465.2:c.371del, XM_011519465.1:c.371del, XM_011519469.2:c.371del, XM_011519469.1:c.371del, XM_011519468.2:c.371del, XM_011519468.1:c.371del, XM_017016199.2:c.371del, XM_017016199.1:c.371del, XM_047425182.1:c.371del, XM_047425181.1:c.302del, NM_001351096.1:c.-175del, NM_001256765.1:c.302del, XM_047425183.1:c.302del, XP_011517768.1:p.Asn124fs, XP_011517763.1:p.Asn124fs, XP_011517765.1:p.Asn124fs, XP_011517764.1:p.Asn101fs, XP_011517767.1:p.Asn124fs, XP_011517771.1:p.Asn124fs, XP_011517770.1:p.Asn124fs, XP_016871688.1:p.Asn124fs, XP_047281138.1:p.Asn124fs, XP_047281137.1:p.Asn101fs, NP_001243694.1:p.Asn101fs, XP_047281139.1:p.Asn101fs

                            14.

                            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

                              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.

                                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

                                  17.

                                  rs1459745022 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    C>A,T [Show Flanks]
                                    Chromosome:
                                    10:5968776 (GRCh38)
                                    10:6010739 (GRCh37)
                                    Canonical SPDI:
                                    NC_000010.11:5968775:C:A,NC_000010.11:5968775:C:T
                                    Gene:
                                    IL15RA (Varview), LOC107984200 (Varview)
                                    Functional Consequence:
                                    coding_sequence_variant,intron_variant,5_prime_UTR_variant,missense_variant
                                    Validated:
                                    by frequency,by cluster
                                    MAF:
                                    T=0.000008/1 (GnomAD_exomes)
                                    HGVS:
                                    NC_000010.11:g.5968776C>A, NC_000010.11:g.5968776C>T, NC_000010.10:g.6010739C>A, NC_000010.10:g.6010739C>T, XM_011519466.3:c.415G>T, XM_011519466.3:c.415G>A, XM_011519466.2:c.415G>T, XM_011519466.2:c.415G>A, XM_011519466.1:c.415G>T, XM_011519466.1:c.415G>A, XM_011519461.3:c.415G>T, XM_011519461.3:c.415G>A, XM_011519461.2:c.415G>T, XM_011519461.2:c.415G>A, XM_011519461.1:c.415G>T, XM_011519461.1:c.415G>A, XM_011519463.3:c.415G>T, XM_011519463.3:c.415G>A, XM_011519463.2:c.415G>T, XM_011519463.2:c.415G>A, XM_011519463.1:c.415G>T, XM_011519463.1:c.415G>A, XM_011519462.3:c.346G>T, XM_011519462.3:c.346G>A, XM_011519462.2:c.346G>T, XM_011519462.2:c.346G>A, XM_011519462.1:c.346G>T, XM_011519462.1:c.346G>A, XM_017016197.3:c.-131G>T, XM_017016197.3:c.-131G>A, XM_017016197.2:c.-131G>T, XM_017016197.2:c.-131G>A, XM_017016197.1:c.-131G>T, XM_017016197.1:c.-131G>A, XM_011519465.2:c.415G>T, XM_011519465.2:c.415G>A, XM_011519465.1:c.415G>T, XM_011519465.1:c.415G>A, XM_011519469.2:c.415G>T, XM_011519469.2:c.415G>A, XM_011519469.1:c.415G>T, XM_011519469.1:c.415G>A, XM_011519468.2:c.415G>T, XM_011519468.2:c.415G>A, XM_011519468.1:c.415G>T, XM_011519468.1:c.415G>A, XM_017016199.2:c.415G>T, XM_017016199.2:c.415G>A, XM_017016199.1:c.415G>T, XM_017016199.1:c.415G>A, XM_047425182.1:c.415G>T, XM_047425182.1:c.415G>A, XM_047425181.1:c.346G>T, XM_047425181.1:c.346G>A, NM_001351096.1:c.-131G>T, NM_001351096.1:c.-131G>A, NM_001256765.1:c.346G>T, NM_001256765.1:c.346G>A, XM_047425183.1:c.346G>T, XM_047425183.1:c.346G>A, XP_011517768.1:p.Gly139Cys, XP_011517768.1:p.Gly139Ser, XP_011517763.1:p.Gly139Cys, XP_011517763.1:p.Gly139Ser, XP_011517765.1:p.Gly139Cys, XP_011517765.1:p.Gly139Ser, XP_011517764.1:p.Gly116Cys, XP_011517764.1:p.Gly116Ser, XP_011517767.1:p.Gly139Cys, XP_011517767.1:p.Gly139Ser, XP_011517771.1:p.Gly139Cys, XP_011517771.1:p.Gly139Ser, XP_011517770.1:p.Gly139Cys, XP_011517770.1:p.Gly139Ser, XP_016871688.1:p.Gly139Cys, XP_016871688.1:p.Gly139Ser, XP_047281138.1:p.Gly139Cys, XP_047281138.1:p.Gly139Ser, XP_047281137.1:p.Gly116Cys, XP_047281137.1:p.Gly116Ser, NP_001243694.1:p.Gly116Cys, NP_001243694.1:p.Gly116Ser, XP_047281139.1:p.Gly116Cys, XP_047281139.1:p.Gly116Ser

                                    18.

                                    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

                                      19.

                                      rs1455727738 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        A>C,G [Show Flanks]
                                        Chromosome:
                                        10:5960442 (GRCh38)
                                        10:6002405 (GRCh37)
                                        Canonical SPDI:
                                        NC_000010.11:5960441:A:C,NC_000010.11:5960441:A:G
                                        Gene:
                                        IL15RA (Varview), LOC107984200 (Varview)
                                        Functional Consequence:
                                        genic_downstream_transcript_variant,missense_variant,downstream_transcript_variant,upstream_transcript_variant,non_coding_transcript_variant,coding_sequence_variant,2KB_upstream_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        G=0./0 (ALFA)
                                        G=0.000004/1 (TOPMED)
                                        G=0.000008/2 (GnomAD_exomes)
                                        HGVS:
                                        NC_000010.11:g.5960442A>C, NC_000010.11:g.5960442A>G, NC_000010.10:g.6002405A>C, NC_000010.10:g.6002405A>G, NM_002189.4:c.508T>G, NM_002189.4:c.508T>C, NM_002189.3:c.508T>G, NM_002189.3:c.508T>C, XM_011519466.3:c.835T>G, XM_011519466.3:c.835T>C, XM_011519466.2:c.835T>G, XM_011519466.2:c.835T>C, XM_011519466.1:c.835T>G, XM_011519466.1:c.835T>C, XM_011519461.3:c.835T>G, XM_011519461.3:c.835T>C, XM_011519461.2:c.835T>G, XM_011519461.2:c.835T>C, XM_011519461.1:c.835T>G, XM_011519461.1:c.835T>C, XM_011519463.3:c.736T>G, XM_011519463.3:c.736T>C, XM_011519463.2:c.736T>G, XM_011519463.2:c.736T>C, XM_011519463.1:c.736T>G, XM_011519463.1:c.736T>C, XM_011519464.3:c.682T>G, XM_011519464.3:c.682T>C, XM_011519464.2:c.682T>G, XM_011519464.2:c.682T>C, XM_011519464.1:c.682T>G, XM_011519464.1:c.682T>C, XM_011519477.3:c.319T>G, XM_011519477.3:c.319T>C, XM_011519477.2:c.319T>G, XM_011519477.2:c.319T>C, XM_011519477.1:c.319T>G, XM_011519477.1:c.319T>C, NM_172200.3:c.409T>G, NM_172200.3:c.409T>C, NM_172200.2:c.409T>G, NM_172200.2:c.409T>C, XM_011519476.3:c.319T>G, XM_011519476.3:c.319T>C, XM_011519476.2:c.319T>G, XM_011519476.2:c.319T>C, XM_011519476.1:c.319T>G, XM_011519476.1:c.319T>C, XM_011519471.3:c.487T>G, XM_011519471.3:c.487T>C, XM_011519471.2:c.487T>G, XM_011519471.2:c.487T>C, XM_011519471.1:c.487T>G, XM_011519471.1:c.487T>C, XM_011519462.3:c.766T>G, XM_011519462.3:c.766T>C, XM_011519462.2:c.766T>G, XM_011519462.2:c.766T>C, XM_011519462.1:c.766T>G, XM_011519462.1:c.766T>C, XM_017016197.3:c.400T>G, XM_017016197.3:c.400T>C, XM_017016197.2:c.400T>G, XM_017016197.2:c.400T>C, XM_017016197.1:c.400T>G, XM_017016197.1:c.400T>C, XM_011519474.3:c.388T>G, XM_011519474.3:c.388T>C, XM_011519474.2:c.388T>G, XM_011519474.2:c.388T>C, XM_011519474.1:c.388T>G, XM_011519474.1:c.388T>C, XM_011519467.3:c.613T>G, XM_011519467.3:c.613T>C, XM_011519467.2:c.613T>G, XM_011519467.2:c.613T>C, XM_011519467.1:c.613T>G, XM_011519467.1:c.613T>C, XM_011519470.3:c.514T>G, XM_011519470.3:c.514T>C, XM_011519470.2:c.514T>G, XM_011519470.2:c.514T>C, XM_011519470.1:c.514T>G, XM_011519470.1:c.514T>C, XM_011519472.3:c.418T>G, XM_011519472.3:c.418T>C, XM_011519472.2:c.418T>G, XM_011519472.2:c.418T>C, XM_011519472.1:c.418T>G, XM_011519472.1:c.418T>C, XM_011519475.3:c.319T>G, XM_011519475.3:c.319T>C, XM_011519475.2:c.319T>G, XM_011519475.2:c.319T>C, XM_011519475.1:c.319T>G, XM_011519475.1:c.319T>C, XM_011519465.2:c.835T>G, XM_011519465.2:c.835T>C, XM_011519465.1:c.835T>G, XM_011519465.1:c.835T>C, XM_011519469.2:c.736T>G, XM_011519469.2:c.736T>C, XM_011519469.1:c.736T>G, XM_011519469.1:c.736T>C, NM_001351095.2:c.583T>G, NM_001351095.2:c.583T>C, NM_001351095.1:c.583T>G, NM_001351095.1:c.583T>C, XM_017016195.2:c.682T>G, XM_017016195.2:c.682T>C, XM_017016195.1:c.682T>G, XM_017016195.1:c.682T>C, XM_017016198.2:c.487T>G, XM_017016198.2:c.487T>C, XM_017016198.1:c.487T>G, XM_017016198.1:c.487T>C, NM_001243539.2:c.400T>G, NM_001243539.2:c.400T>C, NM_001243539.1:c.400T>G, NM_001243539.1:c.400T>C, NM_001351097.2:c.301T>G, NM_001351097.2:c.301T>C, NM_001351097.1:c.301T>G, NM_001351097.1:c.301T>C, XM_011519468.2:c.835T>G, XM_011519468.2:c.835T>C, XM_011519468.1:c.835T>G, XM_011519468.1:c.835T>C, NR_046362.2:n.396T>G, NR_046362.2:n.396T>C, NR_046362.1:n.537T>G, NR_046362.1:n.537T>C, XM_047425182.1:c.736T>G, XM_047425182.1:c.736T>C, XM_047425184.1:c.682T>G, XM_047425184.1:c.682T>C, XM_047425181.1:c.766T>G, XM_047425181.1:c.766T>C, NR_033494.1:n.823T>G, NR_033494.1:n.823T>C, XM_047425185.1:c.400T>G, XM_047425185.1:c.400T>C, NM_001351096.1:c.400T>G, NM_001351096.1:c.400T>C, XM_047425191.1:c.388T>G, XM_047425191.1:c.388T>C, NM_001256765.1:c.766T>G, NM_001256765.1:c.766T>C, XM_047425186.1:c.613T>G, XM_047425186.1:c.613T>C, XM_047425183.1:c.667T>G, XM_047425183.1:c.667T>C, XM_047425187.1:c.514T>G, XM_047425187.1:c.514T>C, XM_047425190.1:c.418T>G, XM_047425190.1:c.418T>C, XM_047425189.1:c.418T>G, XM_047425189.1:c.418T>C, XM_047425188.1:c.514T>G, XM_047425188.1:c.514T>C, NP_002180.1:p.Ser170Ala, NP_002180.1:p.Ser170Pro, XP_011517768.1:p.Ser279Ala, XP_011517768.1:p.Ser279Pro, XP_011517763.1:p.Ser279Ala, XP_011517763.1:p.Ser279Pro, XP_011517765.1:p.Ser246Ala, XP_011517765.1:p.Ser246Pro, XP_011517766.1:p.Ser228Ala, XP_011517766.1:p.Ser228Pro, XP_011517779.1:p.Ser107Ala, XP_011517779.1:p.Ser107Pro, NP_751950.2:p.Ser137Ala, NP_751950.2:p.Ser137Pro, XP_011517778.1:p.Ser107Ala, XP_011517778.1:p.Ser107Pro, XP_011517773.1:p.Ser163Ala, XP_011517773.1:p.Ser163Pro, XP_011517764.1:p.Ser256Ala, XP_011517764.1:p.Ser256Pro, XP_016871686.1:p.Ser134Ala, XP_016871686.1:p.Ser134Pro, XP_011517776.1:p.Ser130Ala, XP_011517776.1:p.Ser130Pro, XP_011517769.1:p.Ser205Ala, XP_011517769.1:p.Ser205Pro, XP_011517772.1:p.Ser172Ala, XP_011517772.1:p.Ser172Pro, XP_011517774.1:p.Ser140Ala, XP_011517774.1:p.Ser140Pro, XP_011517777.1:p.Ser107Ala, XP_011517777.1:p.Ser107Pro, XP_011517767.1:p.Ser279Ala, XP_011517767.1:p.Ser279Pro, XP_011517771.1:p.Ser246Ala, XP_011517771.1:p.Ser246Pro, NP_001338024.1:p.Ser195Ala, NP_001338024.1:p.Ser195Pro, XP_016871684.1:p.Ser228Ala, XP_016871684.1:p.Ser228Pro, XP_016871687.1:p.Ser163Ala, XP_016871687.1:p.Ser163Pro, NP_001230468.1:p.Ser134Ala, NP_001230468.1:p.Ser134Pro, NP_001338026.1:p.Ser101Ala, NP_001338026.1:p.Ser101Pro, XP_011517770.1:p.Ser279Ala, XP_011517770.1:p.Ser279Pro, XP_047281138.1:p.Ser246Ala, XP_047281138.1:p.Ser246Pro, XP_047281140.1:p.Ser228Ala, XP_047281140.1:p.Ser228Pro, XP_047281137.1:p.Ser256Ala, XP_047281137.1:p.Ser256Pro, XP_047281141.1:p.Ser134Ala, XP_047281141.1:p.Ser134Pro, NP_001338025.1:p.Ser134Ala, NP_001338025.1:p.Ser134Pro, XP_047281147.1:p.Ser130Ala, XP_047281147.1:p.Ser130Pro, NP_001243694.1:p.Ser256Ala, NP_001243694.1:p.Ser256Pro, XP_047281142.1:p.Ser205Ala, XP_047281142.1:p.Ser205Pro, XP_047281139.1:p.Ser223Ala, XP_047281139.1:p.Ser223Pro, XP_047281143.1:p.Ser172Ala, XP_047281143.1:p.Ser172Pro, XP_047281146.1:p.Ser140Ala, XP_047281146.1:p.Ser140Pro, XP_047281145.1:p.Ser140Ala, XP_047281145.1:p.Ser140Pro, XP_047281144.1:p.Ser172Ala, XP_047281144.1:p.Ser172Pro

                                        20.

                                        rs1453455227 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          T>C [Show Flanks]
                                          Chromosome:
                                          10:5966167 (GRCh38)
                                          10:6008130 (GRCh37)
                                          Canonical SPDI:
                                          NC_000010.11:5966166:T:C
                                          Gene:
                                          IL15RA (Varview), LOC107984200 (Varview)
                                          Functional Consequence:
                                          coding_sequence_variant,synonymous_variant,intron_variant
                                          Validated:
                                          by frequency,by alfa
                                          MAF:
                                          C=0./0 (ALFA)
                                          C=0.000004/1 (TOPMED)
                                          HGVS:
                                          NC_000010.11:g.5966167T>C, NC_000010.10:g.6008130T>C, NM_002189.4:c.261A>G, NM_002189.3:c.261A>G, XM_011519466.3:c.588A>G, XM_011519466.2:c.588A>G, XM_011519466.1:c.588A>G, XM_011519461.3:c.588A>G, XM_011519461.2:c.588A>G, XM_011519461.1:c.588A>G, XM_011519463.3:c.588A>G, XM_011519463.2:c.588A>G, XM_011519463.1:c.588A>G, XM_011519464.3:c.435A>G, XM_011519464.2:c.435A>G, XM_011519464.1:c.435A>G, NM_172200.3:c.261A>G, NM_172200.2:c.261A>G, XM_011519462.3:c.519A>G, XM_011519462.2:c.519A>G, XM_011519462.1:c.519A>G, XM_017016197.3:c.153A>G, XM_017016197.2:c.153A>G, XM_017016197.1:c.153A>G, XM_011519467.3:c.366A>G, XM_011519467.2:c.366A>G, XM_011519467.1:c.366A>G, XM_011519470.3:c.366A>G, XM_011519470.2:c.366A>G, XM_011519470.1:c.366A>G, XM_011519465.2:c.588A>G, XM_011519465.1:c.588A>G, XM_011519469.2:c.588A>G, XM_011519469.1:c.588A>G, NM_001351095.2:c.435A>G, NM_001351095.1:c.435A>G, XM_017016195.2:c.435A>G, XM_017016195.1:c.435A>G, NM_001243539.2:c.153A>G, NM_001243539.1:c.153A>G, NM_001351097.2:c.153A>G, NM_001351097.1:c.153A>G, XM_011519468.2:c.588A>G, XM_011519468.1:c.588A>G, XM_017016199.2:c.588A>G, XM_017016199.1:c.588A>G, XM_047425182.1:c.588A>G, XM_047425184.1:c.435A>G, XM_047425181.1:c.519A>G, NR_033494.1:n.576A>G, XM_047425185.1:c.153A>G, NM_001351096.1:c.153A>G, NM_001256765.1:c.519A>G, XM_047425186.1:c.366A>G, XM_047425183.1:c.519A>G, XM_047425187.1:c.366A>G, XM_047425188.1:c.366A>G

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