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Items: 1 to 20 of 673

1.

rs1490946222 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>T [Show Flanks]
    Chromosome:
    6:137880131 (GRCh38)
    6:138201268 (GRCh37)
    Canonical SPDI:
    NC_000006.12:137880130:C:T
    Gene:
    TNFAIP3 (Varview)
    Functional Consequence:
    coding_sequence_variant,missense_variant,intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0./0 (ALFA)
    T=0.000004/1 (TOPMED)
    T=0.000007/1 (GnomAD)
    T=0.000342/1 (KOREAN)
    HGVS:

    2.

    rs1490792867 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      T>C [Show Flanks]
      Chromosome:
      6:137874928 (GRCh38)
      6:138196065 (GRCh37)
      Canonical SPDI:
      NC_000006.12:137874927:T:C
      Gene:
      TNFAIP3 (Varview)
      Functional Consequence:
      coding_sequence_variant,missense_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      C=0./0 (ALFA)
      C=0.000004/1 (TOPMED)
      HGVS:
      NC_000006.12:g.137874928T>C, NC_000006.11:g.138196065T>C, NG_032761.1:g.12485T>C, NM_006290.4:c.379T>C, NM_006290.3:c.379T>C, NM_001270508.2:c.379T>C, NM_001270508.1:c.379T>C, NM_001270507.2:c.379T>C, NM_001270507.1:c.379T>C, XM_011536096.3:c.379T>C, XM_011536096.2:c.379T>C, XM_011536096.1:c.379T>C, XM_024446533.2:c.379T>C, XM_024446533.1:c.379T>C, XM_011536095.2:c.379T>C, XM_011536095.1:c.379T>C, XM_024446532.2:c.379T>C, XM_024446532.1:c.379T>C, XM_047419283.1:c.379T>C, XM_047419282.1:c.424T>C, XM_047419285.1:c.379T>C, XM_005267119.1:c.379T>C, XM_047419284.1:c.379T>C, NP_006281.1:p.Phe127Leu, NP_001257437.1:p.Phe127Leu, NP_001257436.1:p.Phe127Leu, XP_011534398.1:p.Phe127Leu, XP_024302301.1:p.Phe127Leu, XP_011534397.1:p.Phe127Leu, XP_024302300.1:p.Phe127Leu, XP_047275239.1:p.Phe127Leu, XP_047275238.1:p.Phe142Leu, XP_047275241.1:p.Phe127Leu, XP_005267176.1:p.Phe127Leu, XP_047275240.1:p.Phe127Leu

      3.

      rs1485694862 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        G>A,C [Show Flanks]
        Chromosome:
        6:137879152 (GRCh38)
        6:138200289 (GRCh37)
        Canonical SPDI:
        NC_000006.12:137879151:G:A,NC_000006.12:137879151:G:C
        Gene:
        TNFAIP3 (Varview)
        Functional Consequence:
        coding_sequence_variant,synonymous_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        A=0.000071/1 (ALFA)
        A=0.000004/1 (TOPMED)
        HGVS:
        NC_000006.12:g.137879152G>A, NC_000006.12:g.137879152G>C, NC_000006.11:g.138200289G>A, NC_000006.11:g.138200289G>C, NG_032761.1:g.16709G>A, NG_032761.1:g.16709G>C, NM_006290.4:c.1707G>A, NM_006290.4:c.1707G>C, NM_006290.3:c.1707G>A, NM_006290.3:c.1707G>C, NM_001270508.2:c.1707G>A, NM_001270508.2:c.1707G>C, NM_001270508.1:c.1707G>A, NM_001270508.1:c.1707G>C, NM_001270507.2:c.1707G>A, NM_001270507.2:c.1707G>C, NM_001270507.1:c.1707G>A, NM_001270507.1:c.1707G>C, XM_011536096.3:c.1707G>A, XM_011536096.3:c.1707G>C, XM_011536096.2:c.1707G>A, XM_011536096.2:c.1707G>C, XM_011536096.1:c.1707G>A, XM_011536096.1:c.1707G>C, XM_024446533.2:c.1707G>A, XM_024446533.2:c.1707G>C, XM_024446533.1:c.1707G>A, XM_024446533.1:c.1707G>C, XM_011536095.2:c.1707G>A, XM_011536095.2:c.1707G>C, XM_011536095.1:c.1707G>A, XM_011536095.1:c.1707G>C, XM_024446532.2:c.1707G>A, XM_024446532.2:c.1707G>C, XM_024446532.1:c.1707G>A, XM_024446532.1:c.1707G>C, XM_047419283.1:c.1707G>A, XM_047419283.1:c.1707G>C, XM_047419282.1:c.1752G>A, XM_047419282.1:c.1752G>C, XM_047419285.1:c.1707G>A, XM_047419285.1:c.1707G>C, XM_005267119.1:c.1707G>A, XM_005267119.1:c.1707G>C, XM_047419284.1:c.1707G>A, XM_047419284.1:c.1707G>C

        4.

        rs1485528552 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          C>A,G,T [Show Flanks]
          Chromosome:
          6:137878635 (GRCh38)
          6:138199772 (GRCh37)
          Canonical SPDI:
          NC_000006.12:137878634:C:A,NC_000006.12:137878634:C:G,NC_000006.12:137878634:C:T
          Gene:
          TNFAIP3 (Varview)
          Functional Consequence:
          coding_sequence_variant,missense_variant
          Validated:
          by frequency,by cluster
          MAF:
          G=0.000004/1 (GnomAD_exomes)
          HGVS:
          NC_000006.12:g.137878635C>A, NC_000006.12:g.137878635C>G, NC_000006.12:g.137878635C>T, NC_000006.11:g.138199772C>A, NC_000006.11:g.138199772C>G, NC_000006.11:g.138199772C>T, NG_032761.1:g.16192C>A, NG_032761.1:g.16192C>G, NG_032761.1:g.16192C>T, NM_006290.4:c.1190C>A, NM_006290.4:c.1190C>G, NM_006290.4:c.1190C>T, NM_006290.3:c.1190C>A, NM_006290.3:c.1190C>G, NM_006290.3:c.1190C>T, NM_001270508.2:c.1190C>A, NM_001270508.2:c.1190C>G, NM_001270508.2:c.1190C>T, NM_001270508.1:c.1190C>A, NM_001270508.1:c.1190C>G, NM_001270508.1:c.1190C>T, NM_001270507.2:c.1190C>A, NM_001270507.2:c.1190C>G, NM_001270507.2:c.1190C>T, NM_001270507.1:c.1190C>A, NM_001270507.1:c.1190C>G, NM_001270507.1:c.1190C>T, XM_011536096.3:c.1190C>A, XM_011536096.3:c.1190C>G, XM_011536096.3:c.1190C>T, XM_011536096.2:c.1190C>A, XM_011536096.2:c.1190C>G, XM_011536096.2:c.1190C>T, XM_011536096.1:c.1190C>A, XM_011536096.1:c.1190C>G, XM_011536096.1:c.1190C>T, XM_024446533.2:c.1190C>A, XM_024446533.2:c.1190C>G, XM_024446533.2:c.1190C>T, XM_024446533.1:c.1190C>A, XM_024446533.1:c.1190C>G, XM_024446533.1:c.1190C>T, XM_011536095.2:c.1190C>A, XM_011536095.2:c.1190C>G, XM_011536095.2:c.1190C>T, XM_011536095.1:c.1190C>A, XM_011536095.1:c.1190C>G, XM_011536095.1:c.1190C>T, XM_024446532.2:c.1190C>A, XM_024446532.2:c.1190C>G, XM_024446532.2:c.1190C>T, XM_024446532.1:c.1190C>A, XM_024446532.1:c.1190C>G, XM_024446532.1:c.1190C>T, XM_047419283.1:c.1190C>A, XM_047419283.1:c.1190C>G, XM_047419283.1:c.1190C>T, XM_047419282.1:c.1235C>A, XM_047419282.1:c.1235C>G, XM_047419282.1:c.1235C>T, XM_047419285.1:c.1190C>A, XM_047419285.1:c.1190C>G, XM_047419285.1:c.1190C>T, XM_005267119.1:c.1190C>A, XM_005267119.1:c.1190C>G, XM_005267119.1:c.1190C>T, XM_047419284.1:c.1190C>A, XM_047419284.1:c.1190C>G, XM_047419284.1:c.1190C>T, NP_006281.1:p.Ser397Tyr, NP_006281.1:p.Ser397Cys, NP_006281.1:p.Ser397Phe, NP_001257437.1:p.Ser397Tyr, NP_001257437.1:p.Ser397Cys, NP_001257437.1:p.Ser397Phe, NP_001257436.1:p.Ser397Tyr, NP_001257436.1:p.Ser397Cys, NP_001257436.1:p.Ser397Phe, XP_011534398.1:p.Ser397Tyr, XP_011534398.1:p.Ser397Cys, XP_011534398.1:p.Ser397Phe, XP_024302301.1:p.Ser397Tyr, XP_024302301.1:p.Ser397Cys, XP_024302301.1:p.Ser397Phe, XP_011534397.1:p.Ser397Tyr, XP_011534397.1:p.Ser397Cys, XP_011534397.1:p.Ser397Phe, XP_024302300.1:p.Ser397Tyr, XP_024302300.1:p.Ser397Cys, XP_024302300.1:p.Ser397Phe, XP_047275239.1:p.Ser397Tyr, XP_047275239.1:p.Ser397Cys, XP_047275239.1:p.Ser397Phe, XP_047275238.1:p.Ser412Tyr, XP_047275238.1:p.Ser412Cys, XP_047275238.1:p.Ser412Phe, XP_047275241.1:p.Ser397Tyr, XP_047275241.1:p.Ser397Cys, XP_047275241.1:p.Ser397Phe, XP_005267176.1:p.Ser397Tyr, XP_005267176.1:p.Ser397Cys, XP_005267176.1:p.Ser397Phe, XP_047275240.1:p.Ser397Tyr, XP_047275240.1:p.Ser397Cys, XP_047275240.1:p.Ser397Phe

          5.

          rs1483594433 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            A>C,G,T [Show Flanks]
            Chromosome:
            6:137881189 (GRCh38)
            6:138202326 (GRCh37)
            Canonical SPDI:
            NC_000006.12:137881188:A:C,NC_000006.12:137881188:A:G,NC_000006.12:137881188:A:T
            Gene:
            TNFAIP3 (Varview)
            Functional Consequence:
            coding_sequence_variant,missense_variant,synonymous_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            G=0.000028/1 (ALFA)
            C=0.000004/1 (TOPMED)
            C=0.000007/1 (GnomAD)
            HGVS:
            NC_000006.12:g.137881189A>C, NC_000006.12:g.137881189A>G, NC_000006.12:g.137881189A>T, NC_000006.11:g.138202326A>C, NC_000006.11:g.138202326A>G, NC_000006.11:g.138202326A>T, NG_032761.1:g.18746A>C, NG_032761.1:g.18746A>G, NG_032761.1:g.18746A>T, NM_006290.4:c.2243A>C, NM_006290.4:c.2243A>G, NM_006290.4:c.2243A>T, NM_006290.3:c.2243A>C, NM_006290.3:c.2243A>G, NM_006290.3:c.2243A>T, NM_001270508.2:c.2243A>C, NM_001270508.2:c.2243A>G, NM_001270508.2:c.2243A>T, NM_001270508.1:c.2243A>C, NM_001270508.1:c.2243A>G, NM_001270508.1:c.2243A>T, NM_001270507.2:c.2243A>C, NM_001270507.2:c.2243A>G, NM_001270507.2:c.2243A>T, NM_001270507.1:c.2243A>C, NM_001270507.1:c.2243A>G, NM_001270507.1:c.2243A>T, XM_011536096.3:c.2061A>C, XM_011536096.3:c.2061A>G, XM_011536096.3:c.2061A>T, XM_011536096.2:c.2061A>C, XM_011536096.2:c.2061A>G, XM_011536096.2:c.2061A>T, XM_011536096.1:c.2061A>C, XM_011536096.1:c.2061A>G, XM_011536096.1:c.2061A>T, XM_024446533.2:c.2243A>C, XM_024446533.2:c.2243A>G, XM_024446533.2:c.2243A>T, XM_024446533.1:c.2243A>C, XM_024446533.1:c.2243A>G, XM_024446533.1:c.2243A>T, XM_011536095.2:c.2243A>C, XM_011536095.2:c.2243A>G, XM_011536095.2:c.2243A>T, XM_011536095.1:c.2243A>C, XM_011536095.1:c.2243A>G, XM_011536095.1:c.2243A>T, XM_024446532.2:c.2243A>C, XM_024446532.2:c.2243A>G, XM_024446532.2:c.2243A>T, XM_024446532.1:c.2243A>C, XM_024446532.1:c.2243A>G, XM_024446532.1:c.2243A>T, XM_047419283.1:c.2243A>C, XM_047419283.1:c.2243A>G, XM_047419283.1:c.2243A>T, XM_047419282.1:c.2288A>C, XM_047419282.1:c.2288A>G, XM_047419282.1:c.2288A>T, XM_047419285.1:c.2061A>C, XM_047419285.1:c.2061A>G, XM_047419285.1:c.2061A>T, XM_005267119.1:c.2243A>C, XM_005267119.1:c.2243A>G, XM_005267119.1:c.2243A>T, XM_047419284.1:c.2061A>C, XM_047419284.1:c.2061A>G, XM_047419284.1:c.2061A>T, NP_006281.1:p.His748Pro, NP_006281.1:p.His748Arg, NP_006281.1:p.His748Leu, NP_001257437.1:p.His748Pro, NP_001257437.1:p.His748Arg, NP_001257437.1:p.His748Leu, NP_001257436.1:p.His748Pro, NP_001257436.1:p.His748Arg, NP_001257436.1:p.His748Leu, XP_024302301.1:p.His748Pro, XP_024302301.1:p.His748Arg, XP_024302301.1:p.His748Leu, XP_011534397.1:p.His748Pro, XP_011534397.1:p.His748Arg, XP_011534397.1:p.His748Leu, XP_024302300.1:p.His748Pro, XP_024302300.1:p.His748Arg, XP_024302300.1:p.His748Leu, XP_047275239.1:p.His748Pro, XP_047275239.1:p.His748Arg, XP_047275239.1:p.His748Leu, XP_047275238.1:p.His763Pro, XP_047275238.1:p.His763Arg, XP_047275238.1:p.His763Leu, XP_005267176.1:p.His748Pro, XP_005267176.1:p.His748Arg, XP_005267176.1:p.His748Leu

            6.

            rs1483266356 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              G>A [Show Flanks]
              Chromosome:
              6:137874922 (GRCh38)
              6:138196059 (GRCh37)
              Canonical SPDI:
              NC_000006.12:137874921:G:A
              Gene:
              TNFAIP3 (Varview)
              Functional Consequence:
              coding_sequence_variant,missense_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              A=0./0 (ALFA)
              A=0./0 (GnomAD)
              A=0.000004/1 (GnomAD_exomes)
              HGVS:
              NC_000006.12:g.137874922G>A, NC_000006.11:g.138196059G>A, NG_032761.1:g.12479G>A, NM_006290.4:c.373G>A, NM_006290.3:c.373G>A, NM_001270508.2:c.373G>A, NM_001270508.1:c.373G>A, NM_001270507.2:c.373G>A, NM_001270507.1:c.373G>A, XM_011536096.3:c.373G>A, XM_011536096.2:c.373G>A, XM_011536096.1:c.373G>A, XM_024446533.2:c.373G>A, XM_024446533.1:c.373G>A, XM_011536095.2:c.373G>A, XM_011536095.1:c.373G>A, XM_024446532.2:c.373G>A, XM_024446532.1:c.373G>A, XM_047419283.1:c.373G>A, XM_047419282.1:c.418G>A, XM_047419285.1:c.373G>A, XM_005267119.1:c.373G>A, XM_047419284.1:c.373G>A, NP_006281.1:p.Ala125Thr, NP_001257437.1:p.Ala125Thr, NP_001257436.1:p.Ala125Thr, XP_011534398.1:p.Ala125Thr, XP_024302301.1:p.Ala125Thr, XP_011534397.1:p.Ala125Thr, XP_024302300.1:p.Ala125Thr, XP_047275239.1:p.Ala125Thr, XP_047275238.1:p.Ala140Thr, XP_047275241.1:p.Ala125Thr, XP_005267176.1:p.Ala125Thr, XP_047275240.1:p.Ala125Thr

              7.

              rs1482254006 [Homo sapiens]
                Variant type:
                DELINS
                Alleles:
                ->T [Show Flanks]
                Chromosome:
                6:137876046 (GRCh38)
                6:138197184 (GRCh37)
                Canonical SPDI:
                NC_000006.12:137876046:T:TT
                Gene:
                TNFAIP3 (Varview)
                Functional Consequence:
                coding_sequence_variant,frameshift_variant
                Validated:
                by frequency,by alfa
                MAF:
                TT=0.0001/1 (ALFA)
                HGVS:
                NC_000006.12:g.137876047dup, NC_000006.11:g.138197184dup, NG_032761.1:g.13604dup, NM_006290.4:c.686dup, NM_006290.3:c.686dup, NM_001270508.2:c.686dup, NM_001270508.1:c.686dup, NM_001270507.2:c.686dup, NM_001270507.1:c.686dup, XM_011536096.3:c.686dup, XM_011536096.2:c.686dup, XM_011536096.1:c.686dup, XM_024446533.2:c.686dup, XM_024446533.1:c.686dup, XM_011536095.2:c.686dup, XM_011536095.1:c.686dup, XM_024446532.2:c.686dup, XM_024446532.1:c.686dup, XM_047419283.1:c.686dup, XM_047419282.1:c.731dup, XM_047419285.1:c.686dup, XM_005267119.1:c.686dup, XM_047419284.1:c.686dup, NP_006281.1:p.Gly231fs, NP_001257437.1:p.Gly231fs, NP_001257436.1:p.Gly231fs, XP_011534398.1:p.Gly231fs, XP_024302301.1:p.Gly231fs, XP_011534397.1:p.Gly231fs, XP_024302300.1:p.Gly231fs, XP_047275239.1:p.Gly231fs, XP_047275238.1:p.Gly246fs, XP_047275241.1:p.Gly231fs, XP_005267176.1:p.Gly231fs, XP_047275240.1:p.Gly231fs

                8.

                rs1482052537 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  G>C [Show Flanks]
                  Chromosome:
                  6:137879308 (GRCh38)
                  6:138200445 (GRCh37)
                  Canonical SPDI:
                  NC_000006.12:137879307:G:C
                  Gene:
                  TNFAIP3 (Varview)
                  Functional Consequence:
                  coding_sequence_variant,missense_variant
                  Validated:
                  by frequency
                  MAF:
                  C=0.000012/3 (GnomAD_exomes)
                  HGVS:
                  NC_000006.12:g.137879308G>C, NC_000006.11:g.138200445G>C, NG_032761.1:g.16865G>C, NM_006290.4:c.1863G>C, NM_006290.3:c.1863G>C, NM_001270508.2:c.1863G>C, NM_001270508.1:c.1863G>C, NM_001270507.2:c.1863G>C, NM_001270507.1:c.1863G>C, XM_011536096.3:c.1863G>C, XM_011536096.2:c.1863G>C, XM_011536096.1:c.1863G>C, XM_024446533.2:c.1863G>C, XM_024446533.1:c.1863G>C, XM_011536095.2:c.1863G>C, XM_011536095.1:c.1863G>C, XM_024446532.2:c.1863G>C, XM_024446532.1:c.1863G>C, XM_047419283.1:c.1863G>C, XM_047419282.1:c.1908G>C, XM_047419285.1:c.1863G>C, XM_005267119.1:c.1863G>C, XM_047419284.1:c.1863G>C, NP_006281.1:p.Lys621Asn, NP_001257437.1:p.Lys621Asn, NP_001257436.1:p.Lys621Asn, XP_011534398.1:p.Lys621Asn, XP_024302301.1:p.Lys621Asn, XP_011534397.1:p.Lys621Asn, XP_024302300.1:p.Lys621Asn, XP_047275239.1:p.Lys621Asn, XP_047275238.1:p.Lys636Asn, XP_047275241.1:p.Lys621Asn, XP_005267176.1:p.Lys621Asn, XP_047275240.1:p.Lys621Asn

                  9.

                  rs1481327273 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    G>T [Show Flanks]
                    Chromosome:
                    6:137879187 (GRCh38)
                    6:138200324 (GRCh37)
                    Canonical SPDI:
                    NC_000006.12:137879186:G:T
                    Gene:
                    TNFAIP3 (Varview)
                    Functional Consequence:
                    coding_sequence_variant,missense_variant
                    Clinical significance:
                    uncertain-significance
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    T=0./0 (ALFA)
                    T=0.000007/1 (GnomAD)
                    HGVS:
                    NC_000006.12:g.137879187G>T, NC_000006.11:g.138200324G>T, NG_032761.1:g.16744G>T, NM_006290.4:c.1742G>T, NM_006290.3:c.1742G>T, NM_001270508.2:c.1742G>T, NM_001270508.1:c.1742G>T, NM_001270507.2:c.1742G>T, NM_001270507.1:c.1742G>T, XM_011536096.3:c.1742G>T, XM_011536096.2:c.1742G>T, XM_011536096.1:c.1742G>T, XM_024446533.2:c.1742G>T, XM_024446533.1:c.1742G>T, XM_011536095.2:c.1742G>T, XM_011536095.1:c.1742G>T, XM_024446532.2:c.1742G>T, XM_024446532.1:c.1742G>T, XM_047419283.1:c.1742G>T, XM_047419282.1:c.1787G>T, XM_047419285.1:c.1742G>T, XM_005267119.1:c.1742G>T, XM_047419284.1:c.1742G>T, NP_006281.1:p.Arg581Ile, NP_001257437.1:p.Arg581Ile, NP_001257436.1:p.Arg581Ile, XP_011534398.1:p.Arg581Ile, XP_024302301.1:p.Arg581Ile, XP_011534397.1:p.Arg581Ile, XP_024302300.1:p.Arg581Ile, XP_047275239.1:p.Arg581Ile, XP_047275238.1:p.Arg596Ile, XP_047275241.1:p.Arg581Ile, XP_005267176.1:p.Arg581Ile, XP_047275240.1:p.Arg581Ile

                    10.

                    rs1481109549 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      C>G,T [Show Flanks]
                      Chromosome:
                      6:137879058 (GRCh38)
                      6:138200195 (GRCh37)
                      Canonical SPDI:
                      NC_000006.12:137879057:C:G,NC_000006.12:137879057:C:T
                      Gene:
                      TNFAIP3 (Varview)
                      Functional Consequence:
                      coding_sequence_variant,missense_variant
                      Validated:
                      by frequency,by cluster
                      MAF:
                      T=0.000004/1 (GnomAD_exomes)
                      HGVS:
                      NC_000006.12:g.137879058C>G, NC_000006.12:g.137879058C>T, NC_000006.11:g.138200195C>G, NC_000006.11:g.138200195C>T, NG_032761.1:g.16615C>G, NG_032761.1:g.16615C>T, NM_006290.4:c.1613C>G, NM_006290.4:c.1613C>T, NM_006290.3:c.1613C>G, NM_006290.3:c.1613C>T, NM_001270508.2:c.1613C>G, NM_001270508.2:c.1613C>T, NM_001270508.1:c.1613C>G, NM_001270508.1:c.1613C>T, NM_001270507.2:c.1613C>G, NM_001270507.2:c.1613C>T, NM_001270507.1:c.1613C>G, NM_001270507.1:c.1613C>T, XM_011536096.3:c.1613C>G, XM_011536096.3:c.1613C>T, XM_011536096.2:c.1613C>G, XM_011536096.2:c.1613C>T, XM_011536096.1:c.1613C>G, XM_011536096.1:c.1613C>T, XM_024446533.2:c.1613C>G, XM_024446533.2:c.1613C>T, XM_024446533.1:c.1613C>G, XM_024446533.1:c.1613C>T, XM_011536095.2:c.1613C>G, XM_011536095.2:c.1613C>T, XM_011536095.1:c.1613C>G, XM_011536095.1:c.1613C>T, XM_024446532.2:c.1613C>G, XM_024446532.2:c.1613C>T, XM_024446532.1:c.1613C>G, XM_024446532.1:c.1613C>T, XM_047419283.1:c.1613C>G, XM_047419283.1:c.1613C>T, XM_047419282.1:c.1658C>G, XM_047419282.1:c.1658C>T, XM_047419285.1:c.1613C>G, XM_047419285.1:c.1613C>T, XM_005267119.1:c.1613C>G, XM_005267119.1:c.1613C>T, XM_047419284.1:c.1613C>G, XM_047419284.1:c.1613C>T, NP_006281.1:p.Thr538Ser, NP_006281.1:p.Thr538Ile, NP_001257437.1:p.Thr538Ser, NP_001257437.1:p.Thr538Ile, NP_001257436.1:p.Thr538Ser, NP_001257436.1:p.Thr538Ile, XP_011534398.1:p.Thr538Ser, XP_011534398.1:p.Thr538Ile, XP_024302301.1:p.Thr538Ser, XP_024302301.1:p.Thr538Ile, XP_011534397.1:p.Thr538Ser, XP_011534397.1:p.Thr538Ile, XP_024302300.1:p.Thr538Ser, XP_024302300.1:p.Thr538Ile, XP_047275239.1:p.Thr538Ser, XP_047275239.1:p.Thr538Ile, XP_047275238.1:p.Thr553Ser, XP_047275238.1:p.Thr553Ile, XP_047275241.1:p.Thr538Ser, XP_047275241.1:p.Thr538Ile, XP_005267176.1:p.Thr538Ser, XP_005267176.1:p.Thr538Ile, XP_047275240.1:p.Thr538Ser, XP_047275240.1:p.Thr538Ile

                      11.

                      rs1478172750 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        C>T [Show Flanks]
                        Chromosome:
                        6:137871357 (GRCh38)
                        6:138192494 (GRCh37)
                        Canonical SPDI:
                        NC_000006.12:137871356:C:T
                        Gene:
                        TNFAIP3 (Varview)
                        Functional Consequence:
                        missense_variant,coding_sequence_variant
                        Validated:
                        by frequency,by cluster
                        MAF:
                        T=0.000004/1 (GnomAD_exomes)
                        HGVS:
                        NC_000006.12:g.137871357C>T, NC_000006.11:g.138192494C>T, NG_032761.1:g.8914C>T, NM_006290.4:c.130C>T, NM_006290.3:c.130C>T, NM_001270508.2:c.130C>T, NM_001270508.1:c.130C>T, NM_001270507.2:c.130C>T, NM_001270507.1:c.130C>T, XM_011536096.3:c.130C>T, XM_011536096.2:c.130C>T, XM_011536096.1:c.130C>T, XM_024446533.2:c.130C>T, XM_024446533.1:c.130C>T, XM_011536095.2:c.130C>T, XM_011536095.1:c.130C>T, XM_024446532.2:c.130C>T, XM_024446532.1:c.130C>T, XM_047419283.1:c.130C>T, XM_047419282.1:c.175C>T, XM_047419285.1:c.130C>T, XM_005267119.1:c.130C>T, XM_047419284.1:c.130C>T, NP_006281.1:p.His44Tyr, NP_001257437.1:p.His44Tyr, NP_001257436.1:p.His44Tyr, XP_011534398.1:p.His44Tyr, XP_024302301.1:p.His44Tyr, XP_011534397.1:p.His44Tyr, XP_024302300.1:p.His44Tyr, XP_047275239.1:p.His44Tyr, XP_047275238.1:p.His59Tyr, XP_047275241.1:p.His44Tyr, XP_005267176.1:p.His44Tyr, XP_047275240.1:p.His44Tyr

                        12.

                        rs1478144126 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          C>T [Show Flanks]
                          Chromosome:
                          6:137876072 (GRCh38)
                          6:138197209 (GRCh37)
                          Canonical SPDI:
                          NC_000006.12:137876071:C:T
                          Gene:
                          TNFAIP3 (Varview)
                          Functional Consequence:
                          synonymous_variant,coding_sequence_variant
                          Validated:
                          by frequency,by cluster
                          MAF:
                          T=0.000004/1 (GnomAD_exomes)
                          HGVS:

                          13.

                          rs1477238294 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            C>T [Show Flanks]
                            Chromosome:
                            6:137881239 (GRCh38)
                            6:138202376 (GRCh37)
                            Canonical SPDI:
                            NC_000006.12:137881238:C:T
                            Gene:
                            TNFAIP3 (Varview)
                            Functional Consequence:
                            3_prime_UTR_variant,missense_variant,coding_sequence_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            T=0.000111/1 (ALFA)
                            T=0.000004/1 (GnomAD_exomes)
                            HGVS:
                            NC_000006.12:g.137881239C>T, NC_000006.11:g.138202376C>T, NG_032761.1:g.18796C>T, NM_006290.4:c.2293C>T, NM_006290.3:c.2293C>T, NM_001270508.2:c.2293C>T, NM_001270508.1:c.2293C>T, NM_001270507.2:c.2293C>T, NM_001270507.1:c.2293C>T, XM_011536096.3:c.*41C>T, XM_011536096.2:c.*41C>T, XM_011536096.1:c.*41C>T, XM_024446533.2:c.2293C>T, XM_024446533.1:c.2293C>T, XM_011536095.2:c.2293C>T, XM_011536095.1:c.2293C>T, XM_024446532.2:c.2293C>T, XM_024446532.1:c.2293C>T, XM_047419283.1:c.2293C>T, XM_047419282.1:c.2338C>T, XM_047419285.1:c.*41C>T, XM_005267119.1:c.2293C>T, XM_047419284.1:c.*41C>T, NP_006281.1:p.Pro765Ser, NP_001257437.1:p.Pro765Ser, NP_001257436.1:p.Pro765Ser, XP_024302301.1:p.Pro765Ser, XP_011534397.1:p.Pro765Ser, XP_024302300.1:p.Pro765Ser, XP_047275239.1:p.Pro765Ser, XP_047275238.1:p.Pro780Ser, XP_005267176.1:p.Pro765Ser

                            14.

                            rs1476970838 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              G>A [Show Flanks]
                              Chromosome:
                              6:137880192 (GRCh38)
                              6:138201329 (GRCh37)
                              Canonical SPDI:
                              NC_000006.12:137880191:G:A
                              Gene:
                              TNFAIP3 (Varview)
                              Functional Consequence:
                              synonymous_variant,coding_sequence_variant,intron_variant
                              Validated:
                              by frequency
                              MAF:
                              A=0.000004/1 (GnomAD_exomes)
                              HGVS:

                              15.

                              rs1476320420 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                A>G [Show Flanks]
                                Chromosome:
                                6:137878880 (GRCh38)
                                6:138200017 (GRCh37)
                                Canonical SPDI:
                                NC_000006.12:137878879:A:G
                                Gene:
                                TNFAIP3 (Varview)
                                Functional Consequence:
                                missense_variant,coding_sequence_variant
                                Validated:
                                by frequency,by alfa
                                MAF:
                                G=0./0 (ALFA)
                                G=0.000004/1 (GnomAD_exomes)
                                HGVS:
                                NC_000006.12:g.137878880A>G, NC_000006.11:g.138200017A>G, NG_032761.1:g.16437A>G, NM_006290.4:c.1435A>G, NM_006290.3:c.1435A>G, NM_001270508.2:c.1435A>G, NM_001270508.1:c.1435A>G, NM_001270507.2:c.1435A>G, NM_001270507.1:c.1435A>G, XM_011536096.3:c.1435A>G, XM_011536096.2:c.1435A>G, XM_011536096.1:c.1435A>G, XM_024446533.2:c.1435A>G, XM_024446533.1:c.1435A>G, XM_011536095.2:c.1435A>G, XM_011536095.1:c.1435A>G, XM_024446532.2:c.1435A>G, XM_024446532.1:c.1435A>G, XM_047419283.1:c.1435A>G, XM_047419282.1:c.1480A>G, XM_047419285.1:c.1435A>G, XM_005267119.1:c.1435A>G, XM_047419284.1:c.1435A>G, NP_006281.1:p.Arg479Gly, NP_001257437.1:p.Arg479Gly, NP_001257436.1:p.Arg479Gly, XP_011534398.1:p.Arg479Gly, XP_024302301.1:p.Arg479Gly, XP_011534397.1:p.Arg479Gly, XP_024302300.1:p.Arg479Gly, XP_047275239.1:p.Arg479Gly, XP_047275238.1:p.Arg494Gly, XP_047275241.1:p.Arg479Gly, XP_005267176.1:p.Arg479Gly, XP_047275240.1:p.Arg479Gly

                                16.

                                rs1476286095 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  T>A,C [Show Flanks]
                                  Chromosome:
                                  6:137874907 (GRCh38)
                                  6:138196044 (GRCh37)
                                  Canonical SPDI:
                                  NC_000006.12:137874906:T:A,NC_000006.12:137874906:T:C
                                  Gene:
                                  TNFAIP3 (Varview)
                                  Functional Consequence:
                                  missense_variant,synonymous_variant,coding_sequence_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  C=0./0 (ALFA)
                                  A=0.000004/1 (TOPMED)
                                  A=0.000007/1 (GnomAD)
                                  HGVS:
                                  NC_000006.12:g.137874907T>A, NC_000006.12:g.137874907T>C, NC_000006.11:g.138196044T>A, NC_000006.11:g.138196044T>C, NG_032761.1:g.12464T>A, NG_032761.1:g.12464T>C, NM_006290.4:c.358T>A, NM_006290.4:c.358T>C, NM_006290.3:c.358T>A, NM_006290.3:c.358T>C, NM_001270508.2:c.358T>A, NM_001270508.2:c.358T>C, NM_001270508.1:c.358T>A, NM_001270508.1:c.358T>C, NM_001270507.2:c.358T>A, NM_001270507.2:c.358T>C, NM_001270507.1:c.358T>A, NM_001270507.1:c.358T>C, XM_011536096.3:c.358T>A, XM_011536096.3:c.358T>C, XM_011536096.2:c.358T>A, XM_011536096.2:c.358T>C, XM_011536096.1:c.358T>A, XM_011536096.1:c.358T>C, XM_024446533.2:c.358T>A, XM_024446533.2:c.358T>C, XM_024446533.1:c.358T>A, XM_024446533.1:c.358T>C, XM_011536095.2:c.358T>A, XM_011536095.2:c.358T>C, XM_011536095.1:c.358T>A, XM_011536095.1:c.358T>C, XM_024446532.2:c.358T>A, XM_024446532.2:c.358T>C, XM_024446532.1:c.358T>A, XM_024446532.1:c.358T>C, XM_047419283.1:c.358T>A, XM_047419283.1:c.358T>C, XM_047419282.1:c.403T>A, XM_047419282.1:c.403T>C, XM_047419285.1:c.358T>A, XM_047419285.1:c.358T>C, XM_005267119.1:c.358T>A, XM_005267119.1:c.358T>C, XM_047419284.1:c.358T>A, XM_047419284.1:c.358T>C, NP_006281.1:p.Leu120Met, NP_001257437.1:p.Leu120Met, NP_001257436.1:p.Leu120Met, XP_011534398.1:p.Leu120Met, XP_024302301.1:p.Leu120Met, XP_011534397.1:p.Leu120Met, XP_024302300.1:p.Leu120Met, XP_047275239.1:p.Leu120Met, XP_047275238.1:p.Leu135Met, XP_047275241.1:p.Leu120Met, XP_005267176.1:p.Leu120Met, XP_047275240.1:p.Leu120Met

                                  17.

                                  rs1474050669 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    C>G [Show Flanks]
                                    Chromosome:
                                    6:137878552 (GRCh38)
                                    6:138199689 (GRCh37)
                                    Canonical SPDI:
                                    NC_000006.12:137878551:C:G
                                    Gene:
                                    TNFAIP3 (Varview)
                                    Functional Consequence:
                                    synonymous_variant,coding_sequence_variant
                                    Validated:
                                    by frequency,by alfa
                                    MAF:
                                    G=0.000047/1 (ALFA)
                                    G=0.000004/1 (GnomAD_exomes)
                                    HGVS:

                                    18.

                                    rs1472782728 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      C>G,T [Show Flanks]
                                      Chromosome:
                                      6:137881178 (GRCh38)
                                      6:138202315 (GRCh37)
                                      Canonical SPDI:
                                      NC_000006.12:137881177:C:G,NC_000006.12:137881177:C:T
                                      Gene:
                                      TNFAIP3 (Varview)
                                      Functional Consequence:
                                      synonymous_variant,missense_variant,coding_sequence_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      G=0./0 (ALFA)
                                      G=0.000004/1 (TOPMED)
                                      G=0.000007/1 (GnomAD)
                                      HGVS:
                                      NC_000006.12:g.137881178C>G, NC_000006.12:g.137881178C>T, NC_000006.11:g.138202315C>G, NC_000006.11:g.138202315C>T, NG_032761.1:g.18735C>G, NG_032761.1:g.18735C>T, NM_006290.4:c.2232C>G, NM_006290.4:c.2232C>T, NM_006290.3:c.2232C>G, NM_006290.3:c.2232C>T, NM_001270508.2:c.2232C>G, NM_001270508.2:c.2232C>T, NM_001270508.1:c.2232C>G, NM_001270508.1:c.2232C>T, NM_001270507.2:c.2232C>G, NM_001270507.2:c.2232C>T, NM_001270507.1:c.2232C>G, NM_001270507.1:c.2232C>T, XM_011536096.3:c.2050C>G, XM_011536096.3:c.2050C>T, XM_011536096.2:c.2050C>G, XM_011536096.2:c.2050C>T, XM_011536096.1:c.2050C>G, XM_011536096.1:c.2050C>T, XM_024446533.2:c.2232C>G, XM_024446533.2:c.2232C>T, XM_024446533.1:c.2232C>G, XM_024446533.1:c.2232C>T, XM_011536095.2:c.2232C>G, XM_011536095.2:c.2232C>T, XM_011536095.1:c.2232C>G, XM_011536095.1:c.2232C>T, XM_024446532.2:c.2232C>G, XM_024446532.2:c.2232C>T, XM_024446532.1:c.2232C>G, XM_024446532.1:c.2232C>T, XM_047419283.1:c.2232C>G, XM_047419283.1:c.2232C>T, XM_047419282.1:c.2277C>G, XM_047419282.1:c.2277C>T, XM_047419285.1:c.2050C>G, XM_047419285.1:c.2050C>T, XM_005267119.1:c.2232C>G, XM_005267119.1:c.2232C>T, XM_047419284.1:c.2050C>G, XM_047419284.1:c.2050C>T, XP_011534398.1:p.Pro684Ala, XP_011534398.1:p.Pro684Ser, XP_047275241.1:p.Pro684Ala, XP_047275241.1:p.Pro684Ser, XP_047275240.1:p.Pro684Ala, XP_047275240.1:p.Pro684Ser

                                      19.

                                      rs1470990172 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        A>G,T [Show Flanks]
                                        Chromosome:
                                        6:137871264 (GRCh38)
                                        6:138192401 (GRCh37)
                                        Canonical SPDI:
                                        NC_000006.12:137871263:A:G,NC_000006.12:137871263:A:T
                                        Gene:
                                        TNFAIP3 (Varview)
                                        Functional Consequence:
                                        missense_variant,coding_sequence_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        G=0./0 (ALFA)
                                        G=0.000014/2 (GnomAD)
                                        HGVS:
                                        NC_000006.12:g.137871264A>G, NC_000006.12:g.137871264A>T, NC_000006.11:g.138192401A>G, NC_000006.11:g.138192401A>T, NG_032761.1:g.8821A>G, NG_032761.1:g.8821A>T, NM_006290.4:c.37A>G, NM_006290.4:c.37A>T, NM_006290.3:c.37A>G, NM_006290.3:c.37A>T, NM_001270508.2:c.37A>G, NM_001270508.2:c.37A>T, NM_001270508.1:c.37A>G, NM_001270508.1:c.37A>T, NM_001270507.2:c.37A>G, NM_001270507.2:c.37A>T, NM_001270507.1:c.37A>G, NM_001270507.1:c.37A>T, XM_011536096.3:c.37A>G, XM_011536096.3:c.37A>T, XM_011536096.2:c.37A>G, XM_011536096.2:c.37A>T, XM_011536096.1:c.37A>G, XM_011536096.1:c.37A>T, XM_024446533.2:c.37A>G, XM_024446533.2:c.37A>T, XM_024446533.1:c.37A>G, XM_024446533.1:c.37A>T, XM_011536095.2:c.37A>G, XM_011536095.2:c.37A>T, XM_011536095.1:c.37A>G, XM_011536095.1:c.37A>T, XM_024446532.2:c.37A>G, XM_024446532.2:c.37A>T, XM_024446532.1:c.37A>G, XM_024446532.1:c.37A>T, XM_047419283.1:c.37A>G, XM_047419283.1:c.37A>T, XM_047419282.1:c.82A>G, XM_047419282.1:c.82A>T, XM_047419285.1:c.37A>G, XM_047419285.1:c.37A>T, XM_005267119.1:c.37A>G, XM_005267119.1:c.37A>T, XM_047419284.1:c.37A>G, XM_047419284.1:c.37A>T, NP_006281.1:p.Ser13Gly, NP_006281.1:p.Ser13Cys, NP_001257437.1:p.Ser13Gly, NP_001257437.1:p.Ser13Cys, NP_001257436.1:p.Ser13Gly, NP_001257436.1:p.Ser13Cys, XP_011534398.1:p.Ser13Gly, XP_011534398.1:p.Ser13Cys, XP_024302301.1:p.Ser13Gly, XP_024302301.1:p.Ser13Cys, XP_011534397.1:p.Ser13Gly, XP_011534397.1:p.Ser13Cys, XP_024302300.1:p.Ser13Gly, XP_024302300.1:p.Ser13Cys, XP_047275239.1:p.Ser13Gly, XP_047275239.1:p.Ser13Cys, XP_047275238.1:p.Ser28Gly, XP_047275238.1:p.Ser28Cys, XP_047275241.1:p.Ser13Gly, XP_047275241.1:p.Ser13Cys, XP_005267176.1:p.Ser13Gly, XP_005267176.1:p.Ser13Cys, XP_047275240.1:p.Ser13Gly, XP_047275240.1:p.Ser13Cys

                                        20.

                                        rs1470094578 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          C>T [Show Flanks]
                                          Chromosome:
                                          6:137878974 (GRCh38)
                                          6:138200111 (GRCh37)
                                          Canonical SPDI:
                                          NC_000006.12:137878973:C:T
                                          Gene:
                                          TNFAIP3 (Varview)
                                          Functional Consequence:
                                          missense_variant,coding_sequence_variant
                                          Validated:
                                          by frequency,by cluster
                                          MAF:
                                          T=0.000004/1 (GnomAD_exomes)
                                          HGVS:
                                          NC_000006.12:g.137878974C>T, NC_000006.11:g.138200111C>T, NG_032761.1:g.16531C>T, NM_006290.4:c.1529C>T, NM_006290.3:c.1529C>T, NM_001270508.2:c.1529C>T, NM_001270508.1:c.1529C>T, NM_001270507.2:c.1529C>T, NM_001270507.1:c.1529C>T, XM_011536096.3:c.1529C>T, XM_011536096.2:c.1529C>T, XM_011536096.1:c.1529C>T, XM_024446533.2:c.1529C>T, XM_024446533.1:c.1529C>T, XM_011536095.2:c.1529C>T, XM_011536095.1:c.1529C>T, XM_024446532.2:c.1529C>T, XM_024446532.1:c.1529C>T, XM_047419283.1:c.1529C>T, XM_047419282.1:c.1574C>T, XM_047419285.1:c.1529C>T, XM_005267119.1:c.1529C>T, XM_047419284.1:c.1529C>T, NP_006281.1:p.Pro510Leu, NP_001257437.1:p.Pro510Leu, NP_001257436.1:p.Pro510Leu, XP_011534398.1:p.Pro510Leu, XP_024302301.1:p.Pro510Leu, XP_011534397.1:p.Pro510Leu, XP_024302300.1:p.Pro510Leu, XP_047275239.1:p.Pro510Leu, XP_047275238.1:p.Pro525Leu, XP_047275241.1:p.Pro510Leu, XP_005267176.1:p.Pro510Leu, XP_047275240.1:p.Pro510Leu

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