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Items: 1 to 20 of 351

1.

rs1490782484 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>G [Show Flanks]
    Chromosome:
    10:112443530 (GRCh38)
    10:114203288 (GRCh37)
    Canonical SPDI:
    NC_000010.11:112443529:C:G
    Gene:
    ZDHHC6 (Varview)
    Functional Consequence:
    missense_variant,non_coding_transcript_variant,coding_sequence_variant,genic_upstream_transcript_variant
    Validated:
    by frequency
    MAF:
    G=0.000008/2 (GnomAD_exomes)
    HGVS:
    NC_000010.11:g.112443530C>G, NC_000010.10:g.114203288C>G, XM_006717949.5:c.344G>C, XM_006717949.4:c.344G>C, XM_006717949.3:c.344G>C, XM_006717949.2:c.344G>C, XM_006717949.1:c.344G>C, XM_011540095.4:c.124G>C, XM_011540095.3:c.124G>C, XM_011540095.2:c.124G>C, XM_011540095.1:c.124G>C, XM_017016564.3:c.344G>C, XM_017016564.2:c.344G>C, XM_017016564.1:c.344G>C, XM_011540091.3:c.344G>C, XM_011540091.2:c.344G>C, XM_011540091.1:c.344G>C, XM_017016566.3:c.332G>C, XM_017016566.2:c.332G>C, XM_017016566.1:c.332G>C, NM_001351082.3:c.344G>C, NM_001351082.2:c.344G>C, NM_001351082.1:c.344G>C, XM_017016562.3:c.332G>C, XM_017016562.2:c.332G>C, XM_017016562.1:c.332G>C, XM_011540093.3:c.124G>C, XM_011540093.2:c.124G>C, XM_011540093.1:c.124G>C, NM_022494.3:c.344G>C, NM_022494.2:c.344G>C, NM_022494.1:c.344G>C, XM_017016563.3:c.332G>C, XM_017016563.2:c.332G>C, XM_017016563.1:c.332G>C, XM_017016568.3:c.124G>C, XM_017016568.2:c.124G>C, XM_017016568.1:c.124G>C, XM_017016567.3:c.332G>C, XM_017016567.2:c.332G>C, XM_017016567.1:c.332G>C, NM_001363544.2:c.344G>C, NM_001363544.1:c.344G>C, NM_001351084.2:c.344G>C, NM_001351084.1:c.344G>C, NR_147045.2:n.768G>C, NR_147045.1:n.813G>C, NM_001303134.2:c.332G>C, NM_001303134.1:c.332G>C, NM_001351083.2:c.344G>C, NM_001351083.1:c.344G>C, NM_001351085.2:c.124G>C, NM_001351085.1:c.124G>C, NM_001351086.2:c.112G>C, NM_001351086.1:c.112G>C, XM_047425657.1:c.344G>C, XR_007061983.1:n.768G>C, XM_047425653.1:c.344G>C, XM_047425660.1:c.112G>C, XM_047425659.1:c.124G>C, XM_047425656.1:c.344G>C, NM_001411066.1:c.344G>C, XM_047425654.1:c.344G>C, XM_047425655.1:c.344G>C, XM_047425661.1:c.124G>C, XM_047425658.1:c.344G>C, XP_006718012.1:p.Cys115Ser, XP_011538397.1:p.Ala42Pro, XP_016872053.1:p.Cys115Ser, XP_011538393.1:p.Cys115Ser, XP_016872055.1:p.Cys111Ser, NP_001338011.1:p.Cys115Ser, XP_016872051.1:p.Cys111Ser, XP_011538395.1:p.Ala42Pro, NP_071939.1:p.Cys115Ser, XP_016872052.1:p.Cys111Ser, XP_016872057.1:p.Ala42Pro, XP_016872056.1:p.Cys111Ser, NP_001350473.1:p.Cys115Ser, NP_001338013.1:p.Cys115Ser, NP_001290063.1:p.Cys111Ser, NP_001338012.1:p.Cys115Ser, NP_001338014.1:p.Ala42Pro, NP_001338015.1:p.Ala38Pro, XP_047281613.1:p.Cys115Ser, XP_047281609.1:p.Cys115Ser, XP_047281616.1:p.Ala38Pro, XP_047281615.1:p.Ala42Pro, XP_047281612.1:p.Cys115Ser, XP_047281610.1:p.Cys115Ser, XP_047281611.1:p.Cys115Ser, XP_047281617.1:p.Ala42Pro, XP_047281614.1:p.Cys115Ser

    2.

    rs1488968450 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      T>- [Show Flanks]
      Chromosome:
      10:112434381 (GRCh38)
      10:114194139 (GRCh37)
      Canonical SPDI:
      NC_000010.11:112434380:TTT:TT
      Gene:
      ZDHHC6 (Varview)
      Functional Consequence:
      frameshift_variant,non_coding_transcript_variant,coding_sequence_variant
      Validated:
      by frequency,by alfa
      MAF:
      TT=0./0 (ALFA)
      -=0.000004/1 (TOPMED)
      HGVS:
      NC_000010.11:g.112434383del, NC_000010.10:g.114194141del, XM_006717949.5:c.657del, XM_006717949.4:c.657del, XM_006717949.3:c.657del, XM_006717949.2:c.657del, XM_006717949.1:c.657del, XM_011540095.4:c.345del, XM_011540095.3:c.345del, XM_011540095.2:c.345del, XM_011540095.1:c.345del, XM_017016564.3:c.819del, XM_017016564.2:c.819del, XM_017016564.1:c.819del, XM_011540091.3:c.819del, XM_011540091.2:c.819del, XM_011540091.1:c.819del, XM_017016566.3:c.807del, XM_017016566.2:c.807del, XM_017016566.1:c.807del, NM_001351082.3:c.819del, NM_001351082.2:c.819del, NM_001351082.1:c.819del, XM_017016562.3:c.807del, XM_017016562.2:c.807del, XM_017016562.1:c.807del, XM_011540093.3:c.507del, XM_011540093.2:c.507del, XM_011540093.1:c.507del, NM_022494.3:c.819del, NM_022494.2:c.819del, NM_022494.1:c.819del, XM_017016563.3:c.807del, XM_017016563.2:c.807del, XM_017016563.1:c.807del, XM_017016568.3:c.507del, XM_017016568.2:c.507del, XM_017016568.1:c.507del, XM_017016567.3:c.645del, XM_017016567.2:c.645del, XM_017016567.1:c.645del, NM_001363544.2:c.819del, NM_001363544.1:c.819del, NM_001351084.2:c.819del, NM_001351084.1:c.819del, NR_147045.2:n.1243del, NR_147045.1:n.1288del, NM_001303134.2:c.807del, NM_001303134.1:c.807del, NM_001351083.2:c.819del, NM_001351083.1:c.819del, NM_001351085.2:c.507del, NM_001351085.1:c.507del, NM_001351086.2:c.495del, NM_001351086.1:c.495del, XM_017016569.2:c.138del, XM_017016569.1:c.138del, XM_047425657.1:c.657del, XR_007061983.1:n.1243del, XM_047425653.1:c.819del, XM_047425660.1:c.495del, XM_047425659.1:c.507del, XM_047425656.1:c.657del, NM_001411066.1:c.657del, XM_047425654.1:c.819del, XM_047425655.1:c.657del, XM_047425661.1:c.345del, XM_047425658.1:c.819del, XP_006718012.1:p.Lys219fs, XP_011538397.1:p.Lys115fs, XP_016872053.1:p.Lys273fs, XP_011538393.1:p.Lys273fs, XP_016872055.1:p.Lys269fs, NP_001338011.1:p.Lys273fs, XP_016872051.1:p.Lys269fs, XP_011538395.1:p.Lys169fs, NP_071939.1:p.Lys273fs, XP_016872052.1:p.Lys269fs, XP_016872057.1:p.Lys169fs, XP_016872056.1:p.Lys215fs, NP_001350473.1:p.Lys273fs, NP_001338013.1:p.Lys273fs, NP_001290063.1:p.Lys269fs, NP_001338012.1:p.Lys273fs, NP_001338014.1:p.Lys169fs, NP_001338015.1:p.Lys165fs, XP_016872058.1:p.Lys46fs, XP_047281613.1:p.Lys219fs, XP_047281609.1:p.Lys273fs, XP_047281616.1:p.Lys165fs, XP_047281615.1:p.Lys169fs, XP_047281612.1:p.Lys219fs, XP_047281610.1:p.Lys273fs, XP_047281611.1:p.Lys219fs, XP_047281617.1:p.Lys115fs, XP_047281614.1:p.Lys273fs

      3.

      rs1485935920 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        C>A [Show Flanks]
        Chromosome:
        10:112434410 (GRCh38)
        10:114194168 (GRCh37)
        Canonical SPDI:
        NC_000010.11:112434409:C:A
        Gene:
        ZDHHC6 (Varview)
        Functional Consequence:
        coding_sequence_variant,missense_variant,non_coding_transcript_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        A=0./0 (ALFA)
        A=0.000004/1 (TOPMED)
        A=0.000007/1 (GnomAD)
        HGVS:
        NC_000010.11:g.112434410C>A, NC_000010.10:g.114194168C>A, XM_006717949.5:c.628G>T, XM_006717949.4:c.628G>T, XM_006717949.3:c.628G>T, XM_006717949.2:c.628G>T, XM_006717949.1:c.628G>T, XM_011540095.4:c.316G>T, XM_011540095.3:c.316G>T, XM_011540095.2:c.316G>T, XM_011540095.1:c.316G>T, XM_017016564.3:c.790G>T, XM_017016564.2:c.790G>T, XM_017016564.1:c.790G>T, XM_011540091.3:c.790G>T, XM_011540091.2:c.790G>T, XM_011540091.1:c.790G>T, XM_017016566.3:c.778G>T, XM_017016566.2:c.778G>T, XM_017016566.1:c.778G>T, NM_001351082.3:c.790G>T, NM_001351082.2:c.790G>T, NM_001351082.1:c.790G>T, XM_017016562.3:c.778G>T, XM_017016562.2:c.778G>T, XM_017016562.1:c.778G>T, XM_011540093.3:c.478G>T, XM_011540093.2:c.478G>T, XM_011540093.1:c.478G>T, NM_022494.3:c.790G>T, NM_022494.2:c.790G>T, NM_022494.1:c.790G>T, XM_017016563.3:c.778G>T, XM_017016563.2:c.778G>T, XM_017016563.1:c.778G>T, XM_017016568.3:c.478G>T, XM_017016568.2:c.478G>T, XM_017016568.1:c.478G>T, XM_017016567.3:c.616G>T, XM_017016567.2:c.616G>T, XM_017016567.1:c.616G>T, NM_001363544.2:c.790G>T, NM_001363544.1:c.790G>T, NM_001351084.2:c.790G>T, NM_001351084.1:c.790G>T, NR_147045.2:n.1214G>T, NR_147045.1:n.1259G>T, NM_001303134.2:c.778G>T, NM_001303134.1:c.778G>T, NM_001351083.2:c.790G>T, NM_001351083.1:c.790G>T, NM_001351085.2:c.478G>T, NM_001351085.1:c.478G>T, NM_001351086.2:c.466G>T, NM_001351086.1:c.466G>T, XM_017016569.2:c.109G>T, XM_017016569.1:c.109G>T, XM_047425657.1:c.628G>T, XR_007061983.1:n.1214G>T, XM_047425653.1:c.790G>T, XM_047425660.1:c.466G>T, XM_047425659.1:c.478G>T, XM_047425656.1:c.628G>T, NM_001411066.1:c.628G>T, XM_047425654.1:c.790G>T, XM_047425655.1:c.628G>T, XM_047425661.1:c.316G>T, XM_047425658.1:c.790G>T, XP_006718012.1:p.Asp210Tyr, XP_011538397.1:p.Asp106Tyr, XP_016872053.1:p.Asp264Tyr, XP_011538393.1:p.Asp264Tyr, XP_016872055.1:p.Asp260Tyr, NP_001338011.1:p.Asp264Tyr, XP_016872051.1:p.Asp260Tyr, XP_011538395.1:p.Asp160Tyr, NP_071939.1:p.Asp264Tyr, XP_016872052.1:p.Asp260Tyr, XP_016872057.1:p.Asp160Tyr, XP_016872056.1:p.Asp206Tyr, NP_001350473.1:p.Asp264Tyr, NP_001338013.1:p.Asp264Tyr, NP_001290063.1:p.Asp260Tyr, NP_001338012.1:p.Asp264Tyr, NP_001338014.1:p.Asp160Tyr, NP_001338015.1:p.Asp156Tyr, XP_016872058.1:p.Asp37Tyr, XP_047281613.1:p.Asp210Tyr, XP_047281609.1:p.Asp264Tyr, XP_047281616.1:p.Asp156Tyr, XP_047281615.1:p.Asp160Tyr, XP_047281612.1:p.Asp210Tyr, XP_047281610.1:p.Asp264Tyr, XP_047281611.1:p.Asp210Tyr, XP_047281617.1:p.Asp106Tyr, XP_047281614.1:p.Asp264Tyr

        4.

        rs1481981648 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          T>C [Show Flanks]
          Chromosome:
          10:112434438 (GRCh38)
          10:114194196 (GRCh37)
          Canonical SPDI:
          NC_000010.11:112434437:T:C
          Gene:
          ZDHHC6 (Varview)
          Functional Consequence:
          coding_sequence_variant,synonymous_variant,non_coding_transcript_variant
          Validated:
          by frequency
          MAF:
          C=0.000004/1 (GnomAD_exomes)
          HGVS:
          NC_000010.11:g.112434438T>C, NC_000010.10:g.114194196T>C, XM_006717949.5:c.600A>G, XM_006717949.4:c.600A>G, XM_006717949.3:c.600A>G, XM_006717949.2:c.600A>G, XM_006717949.1:c.600A>G, XM_011540095.4:c.288A>G, XM_011540095.3:c.288A>G, XM_011540095.2:c.288A>G, XM_011540095.1:c.288A>G, XM_017016564.3:c.762A>G, XM_017016564.2:c.762A>G, XM_017016564.1:c.762A>G, XM_011540091.3:c.762A>G, XM_011540091.2:c.762A>G, XM_011540091.1:c.762A>G, XM_017016566.3:c.750A>G, XM_017016566.2:c.750A>G, XM_017016566.1:c.750A>G, NM_001351082.3:c.762A>G, NM_001351082.2:c.762A>G, NM_001351082.1:c.762A>G, XM_017016562.3:c.750A>G, XM_017016562.2:c.750A>G, XM_017016562.1:c.750A>G, XM_011540093.3:c.450A>G, XM_011540093.2:c.450A>G, XM_011540093.1:c.450A>G, NM_022494.3:c.762A>G, NM_022494.2:c.762A>G, NM_022494.1:c.762A>G, XM_017016563.3:c.750A>G, XM_017016563.2:c.750A>G, XM_017016563.1:c.750A>G, XM_017016568.3:c.450A>G, XM_017016568.2:c.450A>G, XM_017016568.1:c.450A>G, XM_017016567.3:c.588A>G, XM_017016567.2:c.588A>G, XM_017016567.1:c.588A>G, NM_001363544.2:c.762A>G, NM_001363544.1:c.762A>G, NM_001351084.2:c.762A>G, NM_001351084.1:c.762A>G, NR_147045.2:n.1186A>G, NR_147045.1:n.1231A>G, NM_001303134.2:c.750A>G, NM_001303134.1:c.750A>G, NM_001351083.2:c.762A>G, NM_001351083.1:c.762A>G, NM_001351085.2:c.450A>G, NM_001351085.1:c.450A>G, NM_001351086.2:c.438A>G, NM_001351086.1:c.438A>G, XM_017016569.2:c.81A>G, XM_017016569.1:c.81A>G, XM_047425657.1:c.600A>G, XR_007061983.1:n.1186A>G, XM_047425653.1:c.762A>G, XM_047425660.1:c.438A>G, XM_047425659.1:c.450A>G, XM_047425656.1:c.600A>G, NM_001411066.1:c.600A>G, XM_047425654.1:c.762A>G, XM_047425655.1:c.600A>G, XM_047425661.1:c.288A>G, XM_047425658.1:c.762A>G

          5.

          rs1469875782 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            A>G [Show Flanks]
            Chromosome:
            10:112445292 (GRCh38)
            10:114205050 (GRCh37)
            Canonical SPDI:
            NC_000010.11:112445291:A:G
            Gene:
            ZDHHC6 (Varview), VTI1A (Varview)
            Functional Consequence:
            synonymous_variant,upstream_transcript_variant,coding_sequence_variant,non_coding_transcript_variant,5_prime_UTR_variant,genic_upstream_transcript_variant,2KB_upstream_variant
            Validated:
            by frequency
            MAF:
            G=0.000004/1 (GnomAD_exomes)
            HGVS:
            NC_000010.11:g.112445292A>G, NC_000010.10:g.114205050A>G, XM_006717949.5:c.145T>C, XM_006717949.4:c.145T>C, XM_006717949.3:c.145T>C, XM_006717949.2:c.145T>C, XM_006717949.1:c.145T>C, XM_011540095.4:c.-76T>C, XM_011540095.3:c.-76T>C, XM_011540095.2:c.-76T>C, XM_011540095.1:c.-76T>C, XM_017016564.3:c.145T>C, XM_017016564.2:c.145T>C, XM_017016564.1:c.145T>C, XM_011540091.3:c.145T>C, XM_011540091.2:c.145T>C, XM_011540091.1:c.145T>C, XM_017016566.3:c.145T>C, XM_017016566.2:c.145T>C, XM_017016566.1:c.145T>C, NM_001351082.3:c.145T>C, NM_001351082.2:c.145T>C, NM_001351082.1:c.145T>C, XM_017016562.3:c.145T>C, XM_017016562.2:c.145T>C, XM_017016562.1:c.145T>C, XM_011540093.3:c.-76T>C, XM_011540093.2:c.-76T>C, XM_011540093.1:c.-76T>C, NM_022494.3:c.145T>C, NM_022494.2:c.145T>C, NM_022494.1:c.145T>C, XM_017016563.3:c.145T>C, XM_017016563.2:c.145T>C, XM_017016563.1:c.145T>C, XM_017016568.3:c.-76T>C, XM_017016568.2:c.-76T>C, XM_017016568.1:c.-76T>C, XM_017016567.3:c.145T>C, XM_017016567.2:c.145T>C, XM_017016567.1:c.145T>C, NM_001363544.2:c.145T>C, NM_001363544.1:c.145T>C, NM_001351084.2:c.145T>C, NM_001351084.1:c.145T>C, NR_147045.2:n.569T>C, NR_147045.1:n.614T>C, NM_001303134.2:c.145T>C, NM_001303134.1:c.145T>C, NM_001351083.2:c.145T>C, NM_001351083.1:c.145T>C, NM_001351085.2:c.-76T>C, NM_001351085.1:c.-76T>C, NM_001351086.2:c.-76T>C, NM_001351086.1:c.-76T>C, XM_047425657.1:c.145T>C, XR_007061983.1:n.569T>C, XM_047425653.1:c.145T>C, XM_047425660.1:c.-76T>C, XM_047425659.1:c.-76T>C, XM_047425656.1:c.145T>C, NM_001411066.1:c.145T>C, XM_047425654.1:c.145T>C, XM_047425655.1:c.145T>C, XM_047425661.1:c.-76T>C, XM_047425658.1:c.145T>C

            6.

            rs1467247586 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              C>A [Show Flanks]
              Chromosome:
              10:112432439 (GRCh38)
              10:114192197 (GRCh37)
              Canonical SPDI:
              NC_000010.11:112432438:C:A
              Gene:
              ZDHHC6 (Varview)
              Functional Consequence:
              coding_sequence_variant,missense_variant,non_coding_transcript_variant,genic_downstream_transcript_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              A=0.000071/1 (ALFA)
              A=0.000004/1 (GnomAD_exomes)
              HGVS:
              NC_000010.11:g.112432439C>A, NC_000010.10:g.114192197C>A, XM_006717949.5:c.866G>T, XM_006717949.4:c.866G>T, XM_006717949.3:c.866G>T, XM_006717949.2:c.866G>T, XM_006717949.1:c.866G>T, XM_011540095.4:c.554G>T, XM_011540095.3:c.554G>T, XM_011540095.2:c.554G>T, XM_011540095.1:c.554G>T, XM_017016564.3:c.1028G>T, XM_017016564.2:c.1028G>T, XM_017016564.1:c.1028G>T, XM_011540091.3:c.1028G>T, XM_011540091.2:c.1028G>T, XM_011540091.1:c.1028G>T, XM_017016566.3:c.1016G>T, XM_017016566.2:c.1016G>T, XM_017016566.1:c.1016G>T, NM_001351082.3:c.1028G>T, NM_001351082.2:c.1028G>T, NM_001351082.1:c.1028G>T, XM_017016562.3:c.1016G>T, XM_017016562.2:c.1016G>T, XM_017016562.1:c.1016G>T, XM_011540093.3:c.716G>T, XM_011540093.2:c.716G>T, XM_011540093.1:c.716G>T, NM_022494.3:c.1028G>T, NM_022494.2:c.1028G>T, NM_022494.1:c.1028G>T, XM_017016563.3:c.1016G>T, XM_017016563.2:c.1016G>T, XM_017016563.1:c.1016G>T, XM_017016568.3:c.716G>T, XM_017016568.2:c.716G>T, XM_017016568.1:c.716G>T, XM_017016567.3:c.854G>T, XM_017016567.2:c.854G>T, XM_017016567.1:c.854G>T, NM_001363544.2:c.1028G>T, NM_001363544.1:c.1028G>T, NM_001351084.2:c.1028G>T, NM_001351084.1:c.1028G>T, NR_147045.2:n.1528G>T, NR_147045.1:n.1573G>T, NM_001303134.2:c.1016G>T, NM_001303134.1:c.1016G>T, NM_001351083.2:c.1028G>T, NM_001351083.1:c.1028G>T, NM_001351085.2:c.716G>T, NM_001351085.1:c.716G>T, NM_001351086.2:c.704G>T, NM_001351086.1:c.704G>T, XM_017016569.2:c.347G>T, XM_017016569.1:c.347G>T, XM_047425657.1:c.866G>T, XR_007061983.1:n.1452G>T, XM_047425653.1:c.1028G>T, XM_047425660.1:c.704G>T, XM_047425659.1:c.716G>T, XM_047425656.1:c.866G>T, NM_001411066.1:c.866G>T, XM_047425654.1:c.1028G>T, XM_047425655.1:c.866G>T, XM_047425661.1:c.554G>T, XP_006718012.1:p.Cys289Phe, XP_011538397.1:p.Cys185Phe, XP_016872053.1:p.Cys343Phe, XP_011538393.1:p.Cys343Phe, XP_016872055.1:p.Cys339Phe, NP_001338011.1:p.Cys343Phe, XP_016872051.1:p.Cys339Phe, XP_011538395.1:p.Cys239Phe, NP_071939.1:p.Cys343Phe, XP_016872052.1:p.Cys339Phe, XP_016872057.1:p.Cys239Phe, XP_016872056.1:p.Cys285Phe, NP_001350473.1:p.Cys343Phe, NP_001338013.1:p.Cys343Phe, NP_001290063.1:p.Cys339Phe, NP_001338012.1:p.Cys343Phe, NP_001338014.1:p.Cys239Phe, NP_001338015.1:p.Cys235Phe, XP_016872058.1:p.Cys116Phe, XP_047281613.1:p.Cys289Phe, XP_047281609.1:p.Cys343Phe, XP_047281616.1:p.Cys235Phe, XP_047281615.1:p.Cys239Phe, XP_047281612.1:p.Cys289Phe, XP_047281610.1:p.Cys343Phe, XP_047281611.1:p.Cys289Phe, XP_047281617.1:p.Cys185Phe

              7.

              rs1454891483 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                G>A [Show Flanks]
                Chromosome:
                10:112445382 (GRCh38)
                10:114205140 (GRCh37)
                Canonical SPDI:
                NC_000010.11:112445381:G:A
                Gene:
                ZDHHC6 (Varview), VTI1A (Varview)
                Functional Consequence:
                5_prime_UTR_variant,synonymous_variant,genic_upstream_transcript_variant,upstream_transcript_variant,non_coding_transcript_variant,coding_sequence_variant,2KB_upstream_variant
                Validated:
                by frequency
                MAF:
                A=0.000004/1 (GnomAD_exomes)
                HGVS:
                NC_000010.11:g.112445382G>A, NC_000010.10:g.114205140G>A, XM_006717949.5:c.55C>T, XM_006717949.4:c.55C>T, XM_006717949.3:c.55C>T, XM_006717949.2:c.55C>T, XM_006717949.1:c.55C>T, XM_011540095.4:c.-166C>T, XM_011540095.3:c.-166C>T, XM_011540095.2:c.-166C>T, XM_011540095.1:c.-166C>T, XM_017016564.3:c.55C>T, XM_017016564.2:c.55C>T, XM_017016564.1:c.55C>T, XM_011540091.3:c.55C>T, XM_011540091.2:c.55C>T, XM_011540091.1:c.55C>T, XM_017016566.3:c.55C>T, XM_017016566.2:c.55C>T, XM_017016566.1:c.55C>T, NM_001351082.3:c.55C>T, NM_001351082.2:c.55C>T, NM_001351082.1:c.55C>T, XM_017016562.3:c.55C>T, XM_017016562.2:c.55C>T, XM_017016562.1:c.55C>T, XM_011540093.3:c.-166C>T, XM_011540093.2:c.-166C>T, XM_011540093.1:c.-166C>T, NM_022494.3:c.55C>T, NM_022494.2:c.55C>T, NM_022494.1:c.55C>T, XM_017016563.3:c.55C>T, XM_017016563.2:c.55C>T, XM_017016563.1:c.55C>T, XM_017016568.3:c.-166C>T, XM_017016568.2:c.-166C>T, XM_017016568.1:c.-166C>T, XM_017016567.3:c.55C>T, XM_017016567.2:c.55C>T, XM_017016567.1:c.55C>T, NM_001363544.2:c.55C>T, NM_001363544.1:c.55C>T, NM_001351084.2:c.55C>T, NM_001351084.1:c.55C>T, NR_147045.2:n.479C>T, NR_147045.1:n.524C>T, NM_001303134.2:c.55C>T, NM_001303134.1:c.55C>T, NM_001351083.2:c.55C>T, NM_001351083.1:c.55C>T, NM_001351085.2:c.-166C>T, NM_001351085.1:c.-166C>T, NM_001351086.2:c.-166C>T, NM_001351086.1:c.-166C>T, XM_047425657.1:c.55C>T, XR_007061983.1:n.479C>T, XM_047425653.1:c.55C>T, XM_047425660.1:c.-166C>T, XM_047425659.1:c.-166C>T, XM_047425656.1:c.55C>T, NM_001411066.1:c.55C>T, XM_047425654.1:c.55C>T, XM_047425655.1:c.55C>T, XM_047425661.1:c.-166C>T, XM_047425658.1:c.55C>T

                8.

                rs1453568459 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  C>A,G [Show Flanks]
                  Chromosome:
                  10:112432382 (GRCh38)
                  10:114192140 (GRCh37)
                  Canonical SPDI:
                  NC_000010.11:112432381:C:A,NC_000010.11:112432381:C:G
                  Gene:
                  ZDHHC6 (Varview)
                  Functional Consequence:
                  genic_downstream_transcript_variant,coding_sequence_variant,missense_variant,non_coding_transcript_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  A=0./0 (ALFA)
                  G=0.000004/1 (GnomAD_exomes)
                  A=0.000004/1 (TOPMED)
                  A=0.000007/1 (GnomAD)
                  HGVS:
                  NC_000010.11:g.112432382C>A, NC_000010.11:g.112432382C>G, NC_000010.10:g.114192140C>A, NC_000010.10:g.114192140C>G, XM_006717949.5:c.923G>T, XM_006717949.5:c.923G>C, XM_006717949.4:c.923G>T, XM_006717949.4:c.923G>C, XM_006717949.3:c.923G>T, XM_006717949.3:c.923G>C, XM_006717949.2:c.923G>T, XM_006717949.2:c.923G>C, XM_006717949.1:c.923G>T, XM_006717949.1:c.923G>C, XM_011540095.4:c.611G>T, XM_011540095.4:c.611G>C, XM_011540095.3:c.611G>T, XM_011540095.3:c.611G>C, XM_011540095.2:c.611G>T, XM_011540095.2:c.611G>C, XM_011540095.1:c.611G>T, XM_011540095.1:c.611G>C, XM_017016564.3:c.1085G>T, XM_017016564.3:c.1085G>C, XM_017016564.2:c.1085G>T, XM_017016564.2:c.1085G>C, XM_017016564.1:c.1085G>T, XM_017016564.1:c.1085G>C, XM_011540091.3:c.1085G>T, XM_011540091.3:c.1085G>C, XM_011540091.2:c.1085G>T, XM_011540091.2:c.1085G>C, XM_011540091.1:c.1085G>T, XM_011540091.1:c.1085G>C, XM_017016566.3:c.1073G>T, XM_017016566.3:c.1073G>C, XM_017016566.2:c.1073G>T, XM_017016566.2:c.1073G>C, XM_017016566.1:c.1073G>T, XM_017016566.1:c.1073G>C, NM_001351082.3:c.1085G>T, NM_001351082.3:c.1085G>C, NM_001351082.2:c.1085G>T, NM_001351082.2:c.1085G>C, NM_001351082.1:c.1085G>T, NM_001351082.1:c.1085G>C, XM_017016562.3:c.1073G>T, XM_017016562.3:c.1073G>C, XM_017016562.2:c.1073G>T, XM_017016562.2:c.1073G>C, XM_017016562.1:c.1073G>T, XM_017016562.1:c.1073G>C, XM_011540093.3:c.773G>T, XM_011540093.3:c.773G>C, XM_011540093.2:c.773G>T, XM_011540093.2:c.773G>C, XM_011540093.1:c.773G>T, XM_011540093.1:c.773G>C, NM_022494.3:c.1085G>T, NM_022494.3:c.1085G>C, NM_022494.2:c.1085G>T, NM_022494.2:c.1085G>C, NM_022494.1:c.1085G>T, NM_022494.1:c.1085G>C, XM_017016563.3:c.1073G>T, XM_017016563.3:c.1073G>C, XM_017016563.2:c.1073G>T, XM_017016563.2:c.1073G>C, XM_017016563.1:c.1073G>T, XM_017016563.1:c.1073G>C, XM_017016568.3:c.773G>T, XM_017016568.3:c.773G>C, XM_017016568.2:c.773G>T, XM_017016568.2:c.773G>C, XM_017016568.1:c.773G>T, XM_017016568.1:c.773G>C, XM_017016567.3:c.911G>T, XM_017016567.3:c.911G>C, XM_017016567.2:c.911G>T, XM_017016567.2:c.911G>C, XM_017016567.1:c.911G>T, XM_017016567.1:c.911G>C, NM_001363544.2:c.1085G>T, NM_001363544.2:c.1085G>C, NM_001363544.1:c.1085G>T, NM_001363544.1:c.1085G>C, NM_001351084.2:c.1085G>T, NM_001351084.2:c.1085G>C, NM_001351084.1:c.1085G>T, NM_001351084.1:c.1085G>C, NR_147045.2:n.1585G>T, NR_147045.2:n.1585G>C, NR_147045.1:n.1630G>T, NR_147045.1:n.1630G>C, NM_001303134.2:c.1073G>T, NM_001303134.2:c.1073G>C, NM_001303134.1:c.1073G>T, NM_001303134.1:c.1073G>C, NM_001351083.2:c.1085G>T, NM_001351083.2:c.1085G>C, NM_001351083.1:c.1085G>T, NM_001351083.1:c.1085G>C, NM_001351085.2:c.773G>T, NM_001351085.2:c.773G>C, NM_001351085.1:c.773G>T, NM_001351085.1:c.773G>C, NM_001351086.2:c.761G>T, NM_001351086.2:c.761G>C, NM_001351086.1:c.761G>T, NM_001351086.1:c.761G>C, XM_017016569.2:c.404G>T, XM_017016569.2:c.404G>C, XM_017016569.1:c.404G>T, XM_017016569.1:c.404G>C, XM_047425657.1:c.923G>T, XM_047425657.1:c.923G>C, XR_007061983.1:n.1509G>T, XR_007061983.1:n.1509G>C, XM_047425653.1:c.1085G>T, XM_047425653.1:c.1085G>C, XM_047425660.1:c.761G>T, XM_047425660.1:c.761G>C, XM_047425659.1:c.773G>T, XM_047425659.1:c.773G>C, XM_047425656.1:c.923G>T, XM_047425656.1:c.923G>C, NM_001411066.1:c.923G>T, NM_001411066.1:c.923G>C, XM_047425654.1:c.1085G>T, XM_047425654.1:c.1085G>C, XM_047425655.1:c.923G>T, XM_047425655.1:c.923G>C, XM_047425661.1:c.611G>T, XM_047425661.1:c.611G>C, XP_006718012.1:p.Gly308Val, XP_006718012.1:p.Gly308Ala, XP_011538397.1:p.Gly204Val, XP_011538397.1:p.Gly204Ala, XP_016872053.1:p.Gly362Val, XP_016872053.1:p.Gly362Ala, XP_011538393.1:p.Gly362Val, XP_011538393.1:p.Gly362Ala, XP_016872055.1:p.Gly358Val, XP_016872055.1:p.Gly358Ala, NP_001338011.1:p.Gly362Val, NP_001338011.1:p.Gly362Ala, XP_016872051.1:p.Gly358Val, XP_016872051.1:p.Gly358Ala, XP_011538395.1:p.Gly258Val, XP_011538395.1:p.Gly258Ala, NP_071939.1:p.Gly362Val, NP_071939.1:p.Gly362Ala, XP_016872052.1:p.Gly358Val, XP_016872052.1:p.Gly358Ala, XP_016872057.1:p.Gly258Val, XP_016872057.1:p.Gly258Ala, XP_016872056.1:p.Gly304Val, XP_016872056.1:p.Gly304Ala, NP_001350473.1:p.Gly362Val, NP_001350473.1:p.Gly362Ala, NP_001338013.1:p.Gly362Val, NP_001338013.1:p.Gly362Ala, NP_001290063.1:p.Gly358Val, NP_001290063.1:p.Gly358Ala, NP_001338012.1:p.Gly362Val, NP_001338012.1:p.Gly362Ala, NP_001338014.1:p.Gly258Val, NP_001338014.1:p.Gly258Ala, NP_001338015.1:p.Gly254Val, NP_001338015.1:p.Gly254Ala, XP_016872058.1:p.Gly135Val, XP_016872058.1:p.Gly135Ala, XP_047281613.1:p.Gly308Val, XP_047281613.1:p.Gly308Ala, XP_047281609.1:p.Gly362Val, XP_047281609.1:p.Gly362Ala, XP_047281616.1:p.Gly254Val, XP_047281616.1:p.Gly254Ala, XP_047281615.1:p.Gly258Val, XP_047281615.1:p.Gly258Ala, XP_047281612.1:p.Gly308Val, XP_047281612.1:p.Gly308Ala, XP_047281610.1:p.Gly362Val, XP_047281610.1:p.Gly362Ala, XP_047281611.1:p.Gly308Val, XP_047281611.1:p.Gly308Ala, XP_047281617.1:p.Gly204Val, XP_047281617.1:p.Gly204Ala

                  9.

                  rs1451715772 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    G>A,C,T [Show Flanks]
                    Chromosome:
                    10:112445232 (GRCh38)
                    10:114204990 (GRCh37)
                    Canonical SPDI:
                    NC_000010.11:112445231:G:A,NC_000010.11:112445231:G:C,NC_000010.11:112445231:G:T
                    Gene:
                    ZDHHC6 (Varview), VTI1A (Varview)
                    Functional Consequence:
                    5_prime_UTR_variant,genic_upstream_transcript_variant,missense_variant,upstream_transcript_variant,non_coding_transcript_variant,coding_sequence_variant,2KB_upstream_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    T=0./0 (ALFA)
                    C=0.000007/1 (GnomAD)
                    HGVS:
                    NC_000010.11:g.112445232G>A, NC_000010.11:g.112445232G>C, NC_000010.11:g.112445232G>T, NC_000010.10:g.114204990G>A, NC_000010.10:g.114204990G>C, NC_000010.10:g.114204990G>T, XM_006717949.5:c.205C>T, XM_006717949.5:c.205C>G, XM_006717949.5:c.205C>A, XM_006717949.4:c.205C>T, XM_006717949.4:c.205C>G, XM_006717949.4:c.205C>A, XM_006717949.3:c.205C>T, XM_006717949.3:c.205C>G, XM_006717949.3:c.205C>A, XM_006717949.2:c.205C>T, XM_006717949.2:c.205C>G, XM_006717949.2:c.205C>A, XM_006717949.1:c.205C>T, XM_006717949.1:c.205C>G, XM_006717949.1:c.205C>A, XM_011540095.4:c.-16C>T, XM_011540095.4:c.-16C>G, XM_011540095.4:c.-16C>A, XM_011540095.3:c.-16C>T, XM_011540095.3:c.-16C>G, XM_011540095.3:c.-16C>A, XM_011540095.2:c.-16C>T, XM_011540095.2:c.-16C>G, XM_011540095.2:c.-16C>A, XM_011540095.1:c.-16C>T, XM_011540095.1:c.-16C>G, XM_011540095.1:c.-16C>A, XM_017016564.3:c.205C>T, XM_017016564.3:c.205C>G, XM_017016564.3:c.205C>A, XM_017016564.2:c.205C>T, XM_017016564.2:c.205C>G, XM_017016564.2:c.205C>A, XM_017016564.1:c.205C>T, XM_017016564.1:c.205C>G, XM_017016564.1:c.205C>A, XM_011540091.3:c.205C>T, XM_011540091.3:c.205C>G, XM_011540091.3:c.205C>A, XM_011540091.2:c.205C>T, XM_011540091.2:c.205C>G, XM_011540091.2:c.205C>A, XM_011540091.1:c.205C>T, XM_011540091.1:c.205C>G, XM_011540091.1:c.205C>A, XM_017016566.3:c.205C>T, XM_017016566.3:c.205C>G, XM_017016566.3:c.205C>A, XM_017016566.2:c.205C>T, XM_017016566.2:c.205C>G, XM_017016566.2:c.205C>A, XM_017016566.1:c.205C>T, XM_017016566.1:c.205C>G, XM_017016566.1:c.205C>A, NM_001351082.3:c.205C>T, NM_001351082.3:c.205C>G, NM_001351082.3:c.205C>A, NM_001351082.2:c.205C>T, NM_001351082.2:c.205C>G, NM_001351082.2:c.205C>A, NM_001351082.1:c.205C>T, NM_001351082.1:c.205C>G, NM_001351082.1:c.205C>A, XM_017016562.3:c.205C>T, XM_017016562.3:c.205C>G, XM_017016562.3:c.205C>A, XM_017016562.2:c.205C>T, XM_017016562.2:c.205C>G, XM_017016562.2:c.205C>A, XM_017016562.1:c.205C>T, XM_017016562.1:c.205C>G, XM_017016562.1:c.205C>A, XM_011540093.3:c.-16C>T, XM_011540093.3:c.-16C>G, XM_011540093.3:c.-16C>A, XM_011540093.2:c.-16C>T, XM_011540093.2:c.-16C>G, XM_011540093.2:c.-16C>A, XM_011540093.1:c.-16C>T, XM_011540093.1:c.-16C>G, XM_011540093.1:c.-16C>A, NM_022494.3:c.205C>T, NM_022494.3:c.205C>G, NM_022494.3:c.205C>A, NM_022494.2:c.205C>T, NM_022494.2:c.205C>G, NM_022494.2:c.205C>A, NM_022494.1:c.205C>T, NM_022494.1:c.205C>G, NM_022494.1:c.205C>A, XM_017016563.3:c.205C>T, XM_017016563.3:c.205C>G, XM_017016563.3:c.205C>A, XM_017016563.2:c.205C>T, XM_017016563.2:c.205C>G, XM_017016563.2:c.205C>A, XM_017016563.1:c.205C>T, XM_017016563.1:c.205C>G, XM_017016563.1:c.205C>A, XM_017016568.3:c.-16C>T, XM_017016568.3:c.-16C>G, XM_017016568.3:c.-16C>A, XM_017016568.2:c.-16C>T, XM_017016568.2:c.-16C>G, XM_017016568.2:c.-16C>A, XM_017016568.1:c.-16C>T, XM_017016568.1:c.-16C>G, XM_017016568.1:c.-16C>A, XM_017016567.3:c.205C>T, XM_017016567.3:c.205C>G, XM_017016567.3:c.205C>A, XM_017016567.2:c.205C>T, XM_017016567.2:c.205C>G, XM_017016567.2:c.205C>A, XM_017016567.1:c.205C>T, XM_017016567.1:c.205C>G, XM_017016567.1:c.205C>A, NM_001363544.2:c.205C>T, NM_001363544.2:c.205C>G, NM_001363544.2:c.205C>A, NM_001363544.1:c.205C>T, NM_001363544.1:c.205C>G, NM_001363544.1:c.205C>A, NM_001351084.2:c.205C>T, NM_001351084.2:c.205C>G, NM_001351084.2:c.205C>A, NM_001351084.1:c.205C>T, NM_001351084.1:c.205C>G, NM_001351084.1:c.205C>A, NR_147045.2:n.629C>T, NR_147045.2:n.629C>G, NR_147045.2:n.629C>A, NR_147045.1:n.674C>T, NR_147045.1:n.674C>G, NR_147045.1:n.674C>A, NM_001303134.2:c.205C>T, NM_001303134.2:c.205C>G, NM_001303134.2:c.205C>A, NM_001303134.1:c.205C>T, NM_001303134.1:c.205C>G, NM_001303134.1:c.205C>A, NM_001351083.2:c.205C>T, NM_001351083.2:c.205C>G, NM_001351083.2:c.205C>A, NM_001351083.1:c.205C>T, NM_001351083.1:c.205C>G, NM_001351083.1:c.205C>A, NM_001351085.2:c.-16C>T, NM_001351085.2:c.-16C>G, NM_001351085.2:c.-16C>A, NM_001351085.1:c.-16C>T, NM_001351085.1:c.-16C>G, NM_001351085.1:c.-16C>A, NM_001351086.2:c.-16C>T, NM_001351086.2:c.-16C>G, NM_001351086.2:c.-16C>A, NM_001351086.1:c.-16C>T, NM_001351086.1:c.-16C>G, NM_001351086.1:c.-16C>A, XM_047425657.1:c.205C>T, XM_047425657.1:c.205C>G, XM_047425657.1:c.205C>A, XR_007061983.1:n.629C>T, XR_007061983.1:n.629C>G, XR_007061983.1:n.629C>A, XM_047425653.1:c.205C>T, XM_047425653.1:c.205C>G, XM_047425653.1:c.205C>A, XM_047425660.1:c.-16C>T, XM_047425660.1:c.-16C>G, XM_047425660.1:c.-16C>A, XM_047425659.1:c.-16C>T, XM_047425659.1:c.-16C>G, XM_047425659.1:c.-16C>A, XM_047425656.1:c.205C>T, XM_047425656.1:c.205C>G, XM_047425656.1:c.205C>A, NM_001411066.1:c.205C>T, NM_001411066.1:c.205C>G, NM_001411066.1:c.205C>A, XM_047425654.1:c.205C>T, XM_047425654.1:c.205C>G, XM_047425654.1:c.205C>A, XM_047425655.1:c.205C>T, XM_047425655.1:c.205C>G, XM_047425655.1:c.205C>A, XM_047425661.1:c.-16C>T, XM_047425661.1:c.-16C>G, XM_047425661.1:c.-16C>A, XM_047425658.1:c.205C>T, XM_047425658.1:c.205C>G, XM_047425658.1:c.205C>A, XP_006718012.1:p.Leu69Phe, XP_006718012.1:p.Leu69Val, XP_006718012.1:p.Leu69Ile, XP_016872053.1:p.Leu69Phe, XP_016872053.1:p.Leu69Val, XP_016872053.1:p.Leu69Ile, XP_011538393.1:p.Leu69Phe, XP_011538393.1:p.Leu69Val, XP_011538393.1:p.Leu69Ile, XP_016872055.1:p.Leu69Phe, XP_016872055.1:p.Leu69Val, XP_016872055.1:p.Leu69Ile, NP_001338011.1:p.Leu69Phe, NP_001338011.1:p.Leu69Val, NP_001338011.1:p.Leu69Ile, XP_016872051.1:p.Leu69Phe, XP_016872051.1:p.Leu69Val, XP_016872051.1:p.Leu69Ile, NP_071939.1:p.Leu69Phe, NP_071939.1:p.Leu69Val, NP_071939.1:p.Leu69Ile, XP_016872052.1:p.Leu69Phe, XP_016872052.1:p.Leu69Val, XP_016872052.1:p.Leu69Ile, XP_016872056.1:p.Leu69Phe, XP_016872056.1:p.Leu69Val, XP_016872056.1:p.Leu69Ile, NP_001350473.1:p.Leu69Phe, NP_001350473.1:p.Leu69Val, NP_001350473.1:p.Leu69Ile, NP_001338013.1:p.Leu69Phe, NP_001338013.1:p.Leu69Val, NP_001338013.1:p.Leu69Ile, NP_001290063.1:p.Leu69Phe, NP_001290063.1:p.Leu69Val, NP_001290063.1:p.Leu69Ile, NP_001338012.1:p.Leu69Phe, NP_001338012.1:p.Leu69Val, NP_001338012.1:p.Leu69Ile, XP_047281613.1:p.Leu69Phe, XP_047281613.1:p.Leu69Val, XP_047281613.1:p.Leu69Ile, XP_047281609.1:p.Leu69Phe, XP_047281609.1:p.Leu69Val, XP_047281609.1:p.Leu69Ile, XP_047281612.1:p.Leu69Phe, XP_047281612.1:p.Leu69Val, XP_047281612.1:p.Leu69Ile, XP_047281610.1:p.Leu69Phe, XP_047281610.1:p.Leu69Val, XP_047281610.1:p.Leu69Ile, XP_047281611.1:p.Leu69Phe, XP_047281611.1:p.Leu69Val, XP_047281611.1:p.Leu69Ile, XP_047281614.1:p.Leu69Phe, XP_047281614.1:p.Leu69Val, XP_047281614.1:p.Leu69Ile

                    10.

                    rs1451475243 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      A>T [Show Flanks]
                      Chromosome:
                      10:112432248 (GRCh38)
                      10:114192006 (GRCh37)
                      Canonical SPDI:
                      NC_000010.11:112432247:A:T
                      Gene:
                      ZDHHC6 (Varview)
                      Functional Consequence:
                      genic_downstream_transcript_variant,coding_sequence_variant,missense_variant,non_coding_transcript_variant
                      Validated:
                      by frequency
                      MAF:
                      T=0.000004/1 (GnomAD_exomes)
                      HGVS:
                      NC_000010.11:g.112432248A>T, NC_000010.10:g.114192006A>T, XM_006717949.5:c.968T>A, XM_006717949.4:c.968T>A, XM_006717949.3:c.968T>A, XM_006717949.2:c.968T>A, XM_006717949.1:c.968T>A, XM_011540095.4:c.656T>A, XM_011540095.3:c.656T>A, XM_011540095.2:c.656T>A, XM_011540095.1:c.656T>A, XM_017016564.3:c.1130T>A, XM_017016564.2:c.1130T>A, XM_017016564.1:c.1130T>A, XM_011540091.3:c.1130T>A, XM_011540091.2:c.1130T>A, XM_011540091.1:c.1130T>A, XM_017016566.3:c.1118T>A, XM_017016566.2:c.1118T>A, XM_017016566.1:c.1118T>A, NM_001351082.3:c.1130T>A, NM_001351082.2:c.1130T>A, NM_001351082.1:c.1130T>A, XM_017016562.3:c.1118T>A, XM_017016562.2:c.1118T>A, XM_017016562.1:c.1118T>A, XM_011540093.3:c.818T>A, XM_011540093.2:c.818T>A, XM_011540093.1:c.818T>A, NM_022494.3:c.1130T>A, NM_022494.2:c.1130T>A, NM_022494.1:c.1130T>A, XM_017016563.3:c.1118T>A, XM_017016563.2:c.1118T>A, XM_017016563.1:c.1118T>A, XM_017016568.3:c.818T>A, XM_017016568.2:c.818T>A, XM_017016568.1:c.818T>A, XM_017016567.3:c.956T>A, XM_017016567.2:c.956T>A, XM_017016567.1:c.956T>A, NM_001363544.2:c.1130T>A, NM_001363544.1:c.1130T>A, NM_001351084.2:c.1130T>A, NM_001351084.1:c.1130T>A, NR_147045.2:n.1630T>A, NR_147045.1:n.1675T>A, NM_001303134.2:c.1118T>A, NM_001303134.1:c.1118T>A, NM_001351083.2:c.1130T>A, NM_001351083.1:c.1130T>A, NM_001351085.2:c.818T>A, NM_001351085.1:c.818T>A, NM_001351086.2:c.806T>A, NM_001351086.1:c.806T>A, XM_017016569.2:c.449T>A, XM_017016569.1:c.449T>A, XM_047425657.1:c.968T>A, XR_007061983.1:n.1554T>A, XM_047425653.1:c.1130T>A, XM_047425660.1:c.806T>A, XM_047425659.1:c.818T>A, XM_047425656.1:c.968T>A, NM_001411066.1:c.968T>A, XM_047425654.1:c.1130T>A, XM_047425655.1:c.968T>A, XM_047425661.1:c.656T>A, XP_006718012.1:p.Phe323Tyr, XP_011538397.1:p.Phe219Tyr, XP_016872053.1:p.Phe377Tyr, XP_011538393.1:p.Phe377Tyr, XP_016872055.1:p.Phe373Tyr, NP_001338011.1:p.Phe377Tyr, XP_016872051.1:p.Phe373Tyr, XP_011538395.1:p.Phe273Tyr, NP_071939.1:p.Phe377Tyr, XP_016872052.1:p.Phe373Tyr, XP_016872057.1:p.Phe273Tyr, XP_016872056.1:p.Phe319Tyr, NP_001350473.1:p.Phe377Tyr, NP_001338013.1:p.Phe377Tyr, NP_001290063.1:p.Phe373Tyr, NP_001338012.1:p.Phe377Tyr, NP_001338014.1:p.Phe273Tyr, NP_001338015.1:p.Phe269Tyr, XP_016872058.1:p.Phe150Tyr, XP_047281613.1:p.Phe323Tyr, XP_047281609.1:p.Phe377Tyr, XP_047281616.1:p.Phe269Tyr, XP_047281615.1:p.Phe273Tyr, XP_047281612.1:p.Phe323Tyr, XP_047281610.1:p.Phe377Tyr, XP_047281611.1:p.Phe323Tyr, XP_047281617.1:p.Phe219Tyr

                      11.

                      rs1446227208 [Homo sapiens]
                        Variant type:
                        DELINS
                        Alleles:
                        G>- [Show Flanks]
                        Chromosome:
                        10:112443561 (GRCh38)
                        10:114203319 (GRCh37)
                        Canonical SPDI:
                        NC_000010.11:112443560:GG:G
                        Gene:
                        ZDHHC6 (Varview)
                        Functional Consequence:
                        coding_sequence_variant,genic_upstream_transcript_variant,frameshift_variant,non_coding_transcript_variant
                        HGVS:
                        NC_000010.11:g.112443562del, NC_000010.10:g.114203320del, XM_006717949.5:c.313del, XM_006717949.4:c.313del, XM_006717949.3:c.313del, XM_006717949.2:c.313del, XM_006717949.1:c.313del, XM_011540095.4:c.93del, XM_011540095.3:c.93del, XM_011540095.2:c.93del, XM_011540095.1:c.93del, XM_017016564.3:c.313del, XM_017016564.2:c.313del, XM_017016564.1:c.313del, XM_011540091.3:c.313del, XM_011540091.2:c.313del, XM_011540091.1:c.313del, XM_017016566.3:c.301del, XM_017016566.2:c.301del, XM_017016566.1:c.301del, NM_001351082.3:c.313del, NM_001351082.2:c.313del, NM_001351082.1:c.313del, XM_017016562.3:c.301del, XM_017016562.2:c.301del, XM_017016562.1:c.301del, XM_011540093.3:c.93del, XM_011540093.2:c.93del, XM_011540093.1:c.93del, NM_022494.3:c.313del, NM_022494.2:c.313del, NM_022494.1:c.313del, XM_017016563.3:c.301del, XM_017016563.2:c.301del, XM_017016563.1:c.301del, XM_017016568.3:c.93del, XM_017016568.2:c.93del, XM_017016568.1:c.93del, XM_017016567.3:c.301del, XM_017016567.2:c.301del, XM_017016567.1:c.301del, NM_001363544.2:c.313del, NM_001363544.1:c.313del, NM_001351084.2:c.313del, NM_001351084.1:c.313del, NR_147045.2:n.737del, NR_147045.1:n.782del, NM_001303134.2:c.301del, NM_001303134.1:c.301del, NM_001351083.2:c.313del, NM_001351083.1:c.313del, NM_001351085.2:c.93del, NM_001351085.1:c.93del, NM_001351086.2:c.81del, NM_001351086.1:c.81del, XM_047425657.1:c.313del, XR_007061983.1:n.737del, XM_047425653.1:c.313del, XM_047425660.1:c.81del, XM_047425659.1:c.93del, XM_047425656.1:c.313del, NM_001411066.1:c.313del, XM_047425654.1:c.313del, XM_047425655.1:c.313del, XM_047425661.1:c.93del, XM_047425658.1:c.313del, XP_006718012.1:p.Gln105fs, XP_011538397.1:p.Lys32fs, XP_016872053.1:p.Gln105fs, XP_011538393.1:p.Gln105fs, XP_016872055.1:p.Gln101fs, NP_001338011.1:p.Gln105fs, XP_016872051.1:p.Gln101fs, XP_011538395.1:p.Lys32fs, NP_071939.1:p.Gln105fs, XP_016872052.1:p.Gln101fs, XP_016872057.1:p.Lys32fs, XP_016872056.1:p.Gln101fs, NP_001350473.1:p.Gln105fs, NP_001338013.1:p.Gln105fs, NP_001290063.1:p.Gln101fs, NP_001338012.1:p.Gln105fs, NP_001338014.1:p.Lys32fs, NP_001338015.1:p.Lys28fs, XP_047281613.1:p.Gln105fs, XP_047281609.1:p.Gln105fs, XP_047281616.1:p.Lys28fs, XP_047281615.1:p.Lys32fs, XP_047281612.1:p.Gln105fs, XP_047281610.1:p.Gln105fs, XP_047281611.1:p.Gln105fs, XP_047281617.1:p.Lys32fs, XP_047281614.1:p.Gln105fs

                        12.

                        rs1440251149 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          G>A [Show Flanks]
                          Chromosome:
                          10:112434306 (GRCh38)
                          10:114194064 (GRCh37)
                          Canonical SPDI:
                          NC_000010.11:112434305:G:A
                          Gene:
                          ZDHHC6 (Varview)
                          Functional Consequence:
                          non_coding_transcript_variant,coding_sequence_variant,synonymous_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          A=0.000224/1 (ALFA)
                          A=0.000004/1 (GnomAD_exomes)
                          A=0.000223/1 (Estonian)
                          HGVS:
                          NC_000010.11:g.112434306G>A, NC_000010.10:g.114194064G>A, XM_006717949.5:c.732C>T, XM_006717949.4:c.732C>T, XM_006717949.3:c.732C>T, XM_006717949.2:c.732C>T, XM_006717949.1:c.732C>T, XM_011540095.4:c.420C>T, XM_011540095.3:c.420C>T, XM_011540095.2:c.420C>T, XM_011540095.1:c.420C>T, XM_017016564.3:c.894C>T, XM_017016564.2:c.894C>T, XM_017016564.1:c.894C>T, XM_011540091.3:c.894C>T, XM_011540091.2:c.894C>T, XM_011540091.1:c.894C>T, XM_017016566.3:c.882C>T, XM_017016566.2:c.882C>T, XM_017016566.1:c.882C>T, NM_001351082.3:c.894C>T, NM_001351082.2:c.894C>T, NM_001351082.1:c.894C>T, XM_017016562.3:c.882C>T, XM_017016562.2:c.882C>T, XM_017016562.1:c.882C>T, XM_011540093.3:c.582C>T, XM_011540093.2:c.582C>T, XM_011540093.1:c.582C>T, NM_022494.3:c.894C>T, NM_022494.2:c.894C>T, NM_022494.1:c.894C>T, XM_017016563.3:c.882C>T, XM_017016563.2:c.882C>T, XM_017016563.1:c.882C>T, XM_017016568.3:c.582C>T, XM_017016568.2:c.582C>T, XM_017016568.1:c.582C>T, XM_017016567.3:c.720C>T, XM_017016567.2:c.720C>T, XM_017016567.1:c.720C>T, NM_001363544.2:c.894C>T, NM_001363544.1:c.894C>T, NM_001351084.2:c.894C>T, NM_001351084.1:c.894C>T, NR_147045.2:n.1318C>T, NR_147045.1:n.1363C>T, NM_001303134.2:c.882C>T, NM_001303134.1:c.882C>T, NM_001351083.2:c.894C>T, NM_001351083.1:c.894C>T, NM_001351085.2:c.582C>T, NM_001351085.1:c.582C>T, NM_001351086.2:c.570C>T, NM_001351086.1:c.570C>T, XM_017016569.2:c.213C>T, XM_017016569.1:c.213C>T, XM_047425657.1:c.732C>T, XR_007061983.1:n.1318C>T, XM_047425653.1:c.894C>T, XM_047425660.1:c.570C>T, XM_047425659.1:c.582C>T, XM_047425656.1:c.732C>T, NM_001411066.1:c.732C>T, XM_047425654.1:c.894C>T, XM_047425655.1:c.732C>T, XM_047425661.1:c.420C>T, XM_047425658.1:c.894C>T

                          13.

                          rs1439122521 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            T>C [Show Flanks]
                            Chromosome:
                            10:112432284 (GRCh38)
                            10:114192042 (GRCh37)
                            Canonical SPDI:
                            NC_000010.11:112432283:T:C
                            Gene:
                            ZDHHC6 (Varview)
                            Functional Consequence:
                            genic_downstream_transcript_variant,missense_variant,non_coding_transcript_variant,coding_sequence_variant
                            Validated:
                            by frequency,by alfa
                            MAF:
                            C=0./0 (ALFA)
                            C=0.000004/1 (TOPMED)
                            HGVS:
                            NC_000010.11:g.112432284T>C, NC_000010.10:g.114192042T>C, XM_006717949.5:c.932A>G, XM_006717949.4:c.932A>G, XM_006717949.3:c.932A>G, XM_006717949.2:c.932A>G, XM_006717949.1:c.932A>G, XM_011540095.4:c.620A>G, XM_011540095.3:c.620A>G, XM_011540095.2:c.620A>G, XM_011540095.1:c.620A>G, XM_017016564.3:c.1094A>G, XM_017016564.2:c.1094A>G, XM_017016564.1:c.1094A>G, XM_011540091.3:c.1094A>G, XM_011540091.2:c.1094A>G, XM_011540091.1:c.1094A>G, XM_017016566.3:c.1082A>G, XM_017016566.2:c.1082A>G, XM_017016566.1:c.1082A>G, NM_001351082.3:c.1094A>G, NM_001351082.2:c.1094A>G, NM_001351082.1:c.1094A>G, XM_017016562.3:c.1082A>G, XM_017016562.2:c.1082A>G, XM_017016562.1:c.1082A>G, XM_011540093.3:c.782A>G, XM_011540093.2:c.782A>G, XM_011540093.1:c.782A>G, NM_022494.3:c.1094A>G, NM_022494.2:c.1094A>G, NM_022494.1:c.1094A>G, XM_017016563.3:c.1082A>G, XM_017016563.2:c.1082A>G, XM_017016563.1:c.1082A>G, XM_017016568.3:c.782A>G, XM_017016568.2:c.782A>G, XM_017016568.1:c.782A>G, XM_017016567.3:c.920A>G, XM_017016567.2:c.920A>G, XM_017016567.1:c.920A>G, NM_001363544.2:c.1094A>G, NM_001363544.1:c.1094A>G, NM_001351084.2:c.1094A>G, NM_001351084.1:c.1094A>G, NR_147045.2:n.1594A>G, NR_147045.1:n.1639A>G, NM_001303134.2:c.1082A>G, NM_001303134.1:c.1082A>G, NM_001351083.2:c.1094A>G, NM_001351083.1:c.1094A>G, NM_001351085.2:c.782A>G, NM_001351085.1:c.782A>G, NM_001351086.2:c.770A>G, NM_001351086.1:c.770A>G, XM_017016569.2:c.413A>G, XM_017016569.1:c.413A>G, XM_047425657.1:c.932A>G, XR_007061983.1:n.1518A>G, XM_047425653.1:c.1094A>G, XM_047425660.1:c.770A>G, XM_047425659.1:c.782A>G, XM_047425656.1:c.932A>G, NM_001411066.1:c.932A>G, XM_047425654.1:c.1094A>G, XM_047425655.1:c.932A>G, XM_047425661.1:c.620A>G, XP_006718012.1:p.Tyr311Cys, XP_011538397.1:p.Tyr207Cys, XP_016872053.1:p.Tyr365Cys, XP_011538393.1:p.Tyr365Cys, XP_016872055.1:p.Tyr361Cys, NP_001338011.1:p.Tyr365Cys, XP_016872051.1:p.Tyr361Cys, XP_011538395.1:p.Tyr261Cys, NP_071939.1:p.Tyr365Cys, XP_016872052.1:p.Tyr361Cys, XP_016872057.1:p.Tyr261Cys, XP_016872056.1:p.Tyr307Cys, NP_001350473.1:p.Tyr365Cys, NP_001338013.1:p.Tyr365Cys, NP_001290063.1:p.Tyr361Cys, NP_001338012.1:p.Tyr365Cys, NP_001338014.1:p.Tyr261Cys, NP_001338015.1:p.Tyr257Cys, XP_016872058.1:p.Tyr138Cys, XP_047281613.1:p.Tyr311Cys, XP_047281609.1:p.Tyr365Cys, XP_047281616.1:p.Tyr257Cys, XP_047281615.1:p.Tyr261Cys, XP_047281612.1:p.Tyr311Cys, XP_047281610.1:p.Tyr365Cys, XP_047281611.1:p.Tyr311Cys, XP_047281617.1:p.Tyr207Cys

                            14.

                            rs1436186083 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              G>C [Show Flanks]
                              Chromosome:
                              10:112432413 (GRCh38)
                              10:114192171 (GRCh37)
                              Canonical SPDI:
                              NC_000010.11:112432412:G:C
                              Gene:
                              ZDHHC6 (Varview)
                              Functional Consequence:
                              genic_downstream_transcript_variant,missense_variant,non_coding_transcript_variant,coding_sequence_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              C=0./0 (ALFA)
                              C=0.000004/1 (TOPMED)
                              C=0.000007/1 (GnomAD)
                              HGVS:
                              NC_000010.11:g.112432413G>C, NC_000010.10:g.114192171G>C, XM_006717949.5:c.892C>G, XM_006717949.4:c.892C>G, XM_006717949.3:c.892C>G, XM_006717949.2:c.892C>G, XM_006717949.1:c.892C>G, XM_011540095.4:c.580C>G, XM_011540095.3:c.580C>G, XM_011540095.2:c.580C>G, XM_011540095.1:c.580C>G, XM_017016564.3:c.1054C>G, XM_017016564.2:c.1054C>G, XM_017016564.1:c.1054C>G, XM_011540091.3:c.1054C>G, XM_011540091.2:c.1054C>G, XM_011540091.1:c.1054C>G, XM_017016566.3:c.1042C>G, XM_017016566.2:c.1042C>G, XM_017016566.1:c.1042C>G, NM_001351082.3:c.1054C>G, NM_001351082.2:c.1054C>G, NM_001351082.1:c.1054C>G, XM_017016562.3:c.1042C>G, XM_017016562.2:c.1042C>G, XM_017016562.1:c.1042C>G, XM_011540093.3:c.742C>G, XM_011540093.2:c.742C>G, XM_011540093.1:c.742C>G, NM_022494.3:c.1054C>G, NM_022494.2:c.1054C>G, NM_022494.1:c.1054C>G, XM_017016563.3:c.1042C>G, XM_017016563.2:c.1042C>G, XM_017016563.1:c.1042C>G, XM_017016568.3:c.742C>G, XM_017016568.2:c.742C>G, XM_017016568.1:c.742C>G, XM_017016567.3:c.880C>G, XM_017016567.2:c.880C>G, XM_017016567.1:c.880C>G, NM_001363544.2:c.1054C>G, NM_001363544.1:c.1054C>G, NM_001351084.2:c.1054C>G, NM_001351084.1:c.1054C>G, NR_147045.2:n.1554C>G, NR_147045.1:n.1599C>G, NM_001303134.2:c.1042C>G, NM_001303134.1:c.1042C>G, NM_001351083.2:c.1054C>G, NM_001351083.1:c.1054C>G, NM_001351085.2:c.742C>G, NM_001351085.1:c.742C>G, NM_001351086.2:c.730C>G, NM_001351086.1:c.730C>G, XM_017016569.2:c.373C>G, XM_017016569.1:c.373C>G, XM_047425657.1:c.892C>G, XR_007061983.1:n.1478C>G, XM_047425653.1:c.1054C>G, XM_047425660.1:c.730C>G, XM_047425659.1:c.742C>G, XM_047425656.1:c.892C>G, NM_001411066.1:c.892C>G, XM_047425654.1:c.1054C>G, XM_047425655.1:c.892C>G, XM_047425661.1:c.580C>G, XP_006718012.1:p.Gln298Glu, XP_011538397.1:p.Gln194Glu, XP_016872053.1:p.Gln352Glu, XP_011538393.1:p.Gln352Glu, XP_016872055.1:p.Gln348Glu, NP_001338011.1:p.Gln352Glu, XP_016872051.1:p.Gln348Glu, XP_011538395.1:p.Gln248Glu, NP_071939.1:p.Gln352Glu, XP_016872052.1:p.Gln348Glu, XP_016872057.1:p.Gln248Glu, XP_016872056.1:p.Gln294Glu, NP_001350473.1:p.Gln352Glu, NP_001338013.1:p.Gln352Glu, NP_001290063.1:p.Gln348Glu, NP_001338012.1:p.Gln352Glu, NP_001338014.1:p.Gln248Glu, NP_001338015.1:p.Gln244Glu, XP_016872058.1:p.Gln125Glu, XP_047281613.1:p.Gln298Glu, XP_047281609.1:p.Gln352Glu, XP_047281616.1:p.Gln244Glu, XP_047281615.1:p.Gln248Glu, XP_047281612.1:p.Gln298Glu, XP_047281610.1:p.Gln352Glu, XP_047281611.1:p.Gln298Glu, XP_047281617.1:p.Gln194Glu

                              15.

                              rs1436027761 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                T>G [Show Flanks]
                                Chromosome:
                                10:112430878 (GRCh38)
                                10:114190636 (GRCh37)
                                Canonical SPDI:
                                NC_000010.11:112430877:T:G
                                Gene:
                                ZDHHC6 (Varview)
                                Functional Consequence:
                                non_coding_transcript_variant,synonymous_variant,intron_variant,coding_sequence_variant,genic_downstream_transcript_variant
                                Validated:
                                by frequency
                                MAF:
                                G=0.000004/1 (GnomAD_exomes)
                                HGVS:
                                NC_000010.11:g.112430878T>G, NC_000010.10:g.114190636T>G, XM_006717949.5:c.1006A>C, XM_006717949.4:c.1006A>C, XM_006717949.3:c.1006A>C, XM_006717949.2:c.1006A>C, XM_006717949.1:c.1006A>C, XM_011540095.4:c.694A>C, XM_011540095.3:c.694A>C, XM_011540095.2:c.694A>C, XM_011540095.1:c.694A>C, NM_001351082.3:c.1168A>C, NM_001351082.2:c.1168A>C, NM_001351082.1:c.1168A>C, XM_017016562.3:c.1156A>C, XM_017016562.2:c.1156A>C, XM_017016562.1:c.1156A>C, XM_011540093.3:c.856A>C, XM_011540093.2:c.856A>C, XM_011540093.1:c.856A>C, NM_022494.3:c.1168A>C, NM_022494.2:c.1168A>C, NM_022494.1:c.1168A>C, XM_017016563.3:c.1156A>C, XM_017016563.2:c.1156A>C, XM_017016563.1:c.1156A>C, XM_017016568.3:c.856A>C, XM_017016568.2:c.856A>C, XM_017016568.1:c.856A>C, XM_017016567.3:c.994A>C, XM_017016567.2:c.994A>C, XM_017016567.1:c.994A>C, NM_001351084.2:c.1168A>C, NM_001351084.1:c.1168A>C, NR_147045.2:n.1668A>C, NR_147045.1:n.1713A>C, NM_001303134.2:c.1156A>C, NM_001303134.1:c.1156A>C, NM_001351083.2:c.1168A>C, NM_001351083.1:c.1168A>C, NM_001351085.2:c.856A>C, NM_001351085.1:c.856A>C, NM_001351086.2:c.844A>C, NM_001351086.1:c.844A>C, XM_017016569.2:c.487A>C, XM_017016569.1:c.487A>C, XR_007061983.1:n.1592A>C, XM_047425659.1:c.856A>C, XM_047425656.1:c.1006A>C, NM_001411066.1:c.1006A>C, XM_047425655.1:c.1006A>C, XM_047425661.1:c.694A>C

                                16.

                                rs1435350093 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  T>C [Show Flanks]
                                  Chromosome:
                                  10:112433261 (GRCh38)
                                  10:114193019 (GRCh37)
                                  Canonical SPDI:
                                  NC_000010.11:112433260:T:C
                                  Gene:
                                  ZDHHC6 (Varview)
                                  Functional Consequence:
                                  downstream_transcript_variant,non_coding_transcript_variant,synonymous_variant,coding_sequence_variant,genic_downstream_transcript_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  C=0./0 (ALFA)
                                  C=0.000004/1 (TOPMED)
                                  C=0.000007/1 (GnomAD)
                                  HGVS:
                                  NC_000010.11:g.112433261T>C, NC_000010.10:g.114193019T>C, XM_006717949.5:c.762A>G, XM_006717949.4:c.762A>G, XM_006717949.3:c.762A>G, XM_006717949.2:c.762A>G, XM_006717949.1:c.762A>G, XM_011540095.4:c.450A>G, XM_011540095.3:c.450A>G, XM_011540095.2:c.450A>G, XM_011540095.1:c.450A>G, XM_017016564.3:c.924A>G, XM_017016564.2:c.924A>G, XM_017016564.1:c.924A>G, XM_011540091.3:c.924A>G, XM_011540091.2:c.924A>G, XM_011540091.1:c.924A>G, XM_017016566.3:c.912A>G, XM_017016566.2:c.912A>G, XM_017016566.1:c.912A>G, NM_001351082.3:c.924A>G, NM_001351082.2:c.924A>G, NM_001351082.1:c.924A>G, XM_017016562.3:c.912A>G, XM_017016562.2:c.912A>G, XM_017016562.1:c.912A>G, XM_011540093.3:c.612A>G, XM_011540093.2:c.612A>G, XM_011540093.1:c.612A>G, NM_022494.3:c.924A>G, NM_022494.2:c.924A>G, NM_022494.1:c.924A>G, XM_017016563.3:c.912A>G, XM_017016563.2:c.912A>G, XM_017016563.1:c.912A>G, XM_017016568.3:c.612A>G, XM_017016568.2:c.612A>G, XM_017016568.1:c.612A>G, XM_017016567.3:c.750A>G, XM_017016567.2:c.750A>G, XM_017016567.1:c.750A>G, NM_001363544.2:c.924A>G, NM_001363544.1:c.924A>G, NM_001351084.2:c.924A>G, NM_001351084.1:c.924A>G, NR_147045.2:n.1424A>G, NR_147045.1:n.1469A>G, NM_001303134.2:c.912A>G, NM_001303134.1:c.912A>G, NM_001351083.2:c.924A>G, NM_001351083.1:c.924A>G, NM_001351085.2:c.612A>G, NM_001351085.1:c.612A>G, NM_001351086.2:c.600A>G, NM_001351086.1:c.600A>G, XM_017016569.2:c.243A>G, XM_017016569.1:c.243A>G, XM_047425657.1:c.762A>G, XR_007061983.1:n.1348A>G, XM_047425653.1:c.924A>G, XM_047425660.1:c.600A>G, XM_047425659.1:c.612A>G, XM_047425656.1:c.762A>G, NM_001411066.1:c.762A>G, XM_047425654.1:c.924A>G, XM_047425655.1:c.762A>G, XM_047425661.1:c.450A>G

                                  17.

                                  rs1433355146 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    G>A [Show Flanks]
                                    Chromosome:
                                    10:112432283 (GRCh38)
                                    10:114192041 (GRCh37)
                                    Canonical SPDI:
                                    NC_000010.11:112432282:G:A
                                    Gene:
                                    ZDHHC6 (Varview)
                                    Functional Consequence:
                                    genic_downstream_transcript_variant,non_coding_transcript_variant,coding_sequence_variant,synonymous_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    A=0./0 (ALFA)
                                    A=0.000007/1 (GnomAD)
                                    A=0.000008/2 (GnomAD_exomes)
                                    A=0.000008/2 (TOPMED)
                                    A=0.000035/1 (TOMMO)
                                    HGVS:
                                    NC_000010.11:g.112432283G>A, NC_000010.10:g.114192041G>A, XM_006717949.5:c.933C>T, XM_006717949.4:c.933C>T, XM_006717949.3:c.933C>T, XM_006717949.2:c.933C>T, XM_006717949.1:c.933C>T, XM_011540095.4:c.621C>T, XM_011540095.3:c.621C>T, XM_011540095.2:c.621C>T, XM_011540095.1:c.621C>T, XM_017016564.3:c.1095C>T, XM_017016564.2:c.1095C>T, XM_017016564.1:c.1095C>T, XM_011540091.3:c.1095C>T, XM_011540091.2:c.1095C>T, XM_011540091.1:c.1095C>T, XM_017016566.3:c.1083C>T, XM_017016566.2:c.1083C>T, XM_017016566.1:c.1083C>T, NM_001351082.3:c.1095C>T, NM_001351082.2:c.1095C>T, NM_001351082.1:c.1095C>T, XM_017016562.3:c.1083C>T, XM_017016562.2:c.1083C>T, XM_017016562.1:c.1083C>T, XM_011540093.3:c.783C>T, XM_011540093.2:c.783C>T, XM_011540093.1:c.783C>T, NM_022494.3:c.1095C>T, NM_022494.2:c.1095C>T, NM_022494.1:c.1095C>T, XM_017016563.3:c.1083C>T, XM_017016563.2:c.1083C>T, XM_017016563.1:c.1083C>T, XM_017016568.3:c.783C>T, XM_017016568.2:c.783C>T, XM_017016568.1:c.783C>T, XM_017016567.3:c.921C>T, XM_017016567.2:c.921C>T, XM_017016567.1:c.921C>T, NM_001363544.2:c.1095C>T, NM_001363544.1:c.1095C>T, NM_001351084.2:c.1095C>T, NM_001351084.1:c.1095C>T, NR_147045.2:n.1595C>T, NR_147045.1:n.1640C>T, NM_001303134.2:c.1083C>T, NM_001303134.1:c.1083C>T, NM_001351083.2:c.1095C>T, NM_001351083.1:c.1095C>T, NM_001351085.2:c.783C>T, NM_001351085.1:c.783C>T, NM_001351086.2:c.771C>T, NM_001351086.1:c.771C>T, XM_017016569.2:c.414C>T, XM_017016569.1:c.414C>T, XM_047425657.1:c.933C>T, XR_007061983.1:n.1519C>T, XM_047425653.1:c.1095C>T, XM_047425660.1:c.771C>T, XM_047425659.1:c.783C>T, XM_047425656.1:c.933C>T, NM_001411066.1:c.933C>T, XM_047425654.1:c.1095C>T, XM_047425655.1:c.933C>T, XM_047425661.1:c.621C>T

                                    18.

                                    rs1432970790 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      T>C [Show Flanks]
                                      Chromosome:
                                      10:112442331 (GRCh38)
                                      10:114202089 (GRCh37)
                                      Canonical SPDI:
                                      NC_000010.11:112442330:T:C
                                      Gene:
                                      ZDHHC6 (Varview)
                                      Functional Consequence:
                                      non_coding_transcript_variant,genic_upstream_transcript_variant,intron_variant,coding_sequence_variant,missense_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      C=0./0 (ALFA)
                                      C=0.000004/1 (TOPMED)
                                      C=0.000007/1 (GnomAD)
                                      C=0.000008/2 (GnomAD_exomes)
                                      HGVS:
                                      NC_000010.11:g.112442331T>C, NC_000010.10:g.114202089T>C, XM_006717949.5:c.380A>G, XM_006717949.4:c.380A>G, XM_006717949.3:c.380A>G, XM_006717949.2:c.380A>G, XM_006717949.1:c.380A>G, XM_017016564.3:c.380A>G, XM_017016564.2:c.380A>G, XM_017016564.1:c.380A>G, XM_011540091.3:c.380A>G, XM_011540091.2:c.380A>G, XM_011540091.1:c.380A>G, XM_017016566.3:c.368A>G, XM_017016566.2:c.368A>G, XM_017016566.1:c.368A>G, NM_001351082.3:c.380A>G, NM_001351082.2:c.380A>G, NM_001351082.1:c.380A>G, XM_017016562.3:c.368A>G, XM_017016562.2:c.368A>G, XM_017016562.1:c.368A>G, NM_022494.3:c.380A>G, NM_022494.2:c.380A>G, NM_022494.1:c.380A>G, XM_017016563.3:c.368A>G, XM_017016563.2:c.368A>G, XM_017016563.1:c.368A>G, XM_017016567.3:c.368A>G, XM_017016567.2:c.368A>G, XM_017016567.1:c.368A>G, NM_001363544.2:c.380A>G, NM_001363544.1:c.380A>G, NM_001351084.2:c.380A>G, NM_001351084.1:c.380A>G, NR_147045.2:n.804A>G, NR_147045.1:n.849A>G, NM_001303134.2:c.368A>G, NM_001303134.1:c.368A>G, NM_001351083.2:c.380A>G, NM_001351083.1:c.380A>G, XM_047425657.1:c.380A>G, XR_007061983.1:n.804A>G, XM_047425653.1:c.380A>G, XM_047425656.1:c.380A>G, NM_001411066.1:c.380A>G, XM_047425654.1:c.380A>G, XM_047425655.1:c.380A>G, XM_047425658.1:c.380A>G, XP_006718012.1:p.His127Arg, XP_016872053.1:p.His127Arg, XP_011538393.1:p.His127Arg, XP_016872055.1:p.His123Arg, NP_001338011.1:p.His127Arg, XP_016872051.1:p.His123Arg, NP_071939.1:p.His127Arg, XP_016872052.1:p.His123Arg, XP_016872056.1:p.His123Arg, NP_001350473.1:p.His127Arg, NP_001338013.1:p.His127Arg, NP_001290063.1:p.His123Arg, NP_001338012.1:p.His127Arg, XP_047281613.1:p.His127Arg, XP_047281609.1:p.His127Arg, XP_047281612.1:p.His127Arg, XP_047281610.1:p.His127Arg, XP_047281611.1:p.His127Arg, XP_047281614.1:p.His127Arg

                                      19.

                                      rs1432118215 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        A>G [Show Flanks]
                                        Chromosome:
                                        10:112438362 (GRCh38)
                                        10:114198120 (GRCh37)
                                        Canonical SPDI:
                                        NC_000010.11:112438361:A:G
                                        Gene:
                                        ZDHHC6 (Varview)
                                        Functional Consequence:
                                        missense_variant,non_coding_transcript_variant,coding_sequence_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        G=0./0 (ALFA)
                                        G=0.000007/1 (GnomAD)
                                        G=0.000011/3 (TOPMED)
                                        HGVS:
                                        NC_000010.11:g.112438362A>G, NC_000010.10:g.114198120A>G, XM_006717949.5:c.547T>C, XM_006717949.4:c.547T>C, XM_006717949.3:c.547T>C, XM_006717949.2:c.547T>C, XM_006717949.1:c.547T>C, XM_011540095.4:c.235T>C, XM_011540095.3:c.235T>C, XM_011540095.2:c.235T>C, XM_011540095.1:c.235T>C, XM_017016564.3:c.709T>C, XM_017016564.2:c.709T>C, XM_017016564.1:c.709T>C, XM_011540091.3:c.709T>C, XM_011540091.2:c.709T>C, XM_011540091.1:c.709T>C, XM_017016566.3:c.697T>C, XM_017016566.2:c.697T>C, XM_017016566.1:c.697T>C, NM_001351082.3:c.709T>C, NM_001351082.2:c.709T>C, NM_001351082.1:c.709T>C, XM_017016562.3:c.697T>C, XM_017016562.2:c.697T>C, XM_017016562.1:c.697T>C, XM_011540093.3:c.397T>C, XM_011540093.2:c.397T>C, XM_011540093.1:c.397T>C, NM_022494.3:c.709T>C, NM_022494.2:c.709T>C, NM_022494.1:c.709T>C, XM_017016563.3:c.697T>C, XM_017016563.2:c.697T>C, XM_017016563.1:c.697T>C, XM_017016568.3:c.397T>C, XM_017016568.2:c.397T>C, XM_017016568.1:c.397T>C, XM_017016567.3:c.535T>C, XM_017016567.2:c.535T>C, XM_017016567.1:c.535T>C, NM_001363544.2:c.709T>C, NM_001363544.1:c.709T>C, NM_001351084.2:c.709T>C, NM_001351084.1:c.709T>C, NR_147045.2:n.1133T>C, NR_147045.1:n.1178T>C, NM_001303134.2:c.697T>C, NM_001303134.1:c.697T>C, NM_001351083.2:c.709T>C, NM_001351083.1:c.709T>C, NM_001351085.2:c.397T>C, NM_001351085.1:c.397T>C, NM_001351086.2:c.385T>C, NM_001351086.1:c.385T>C, XM_017016569.2:c.28T>C, XM_017016569.1:c.28T>C, XM_047425657.1:c.547T>C, XR_007061983.1:n.1133T>C, XM_047425653.1:c.709T>C, XM_047425660.1:c.385T>C, XM_047425659.1:c.397T>C, XM_047425656.1:c.547T>C, NM_001411066.1:c.547T>C, XM_047425654.1:c.709T>C, XM_047425655.1:c.547T>C, XM_047425661.1:c.235T>C, XM_047425658.1:c.709T>C, XP_006718012.1:p.Ser183Pro, XP_011538397.1:p.Ser79Pro, XP_016872053.1:p.Ser237Pro, XP_011538393.1:p.Ser237Pro, XP_016872055.1:p.Ser233Pro, NP_001338011.1:p.Ser237Pro, XP_016872051.1:p.Ser233Pro, XP_011538395.1:p.Ser133Pro, NP_071939.1:p.Ser237Pro, XP_016872052.1:p.Ser233Pro, XP_016872057.1:p.Ser133Pro, XP_016872056.1:p.Ser179Pro, NP_001350473.1:p.Ser237Pro, NP_001338013.1:p.Ser237Pro, NP_001290063.1:p.Ser233Pro, NP_001338012.1:p.Ser237Pro, NP_001338014.1:p.Ser133Pro, NP_001338015.1:p.Ser129Pro, XP_016872058.1:p.Ser10Pro, XP_047281613.1:p.Ser183Pro, XP_047281609.1:p.Ser237Pro, XP_047281616.1:p.Ser129Pro, XP_047281615.1:p.Ser133Pro, XP_047281612.1:p.Ser183Pro, XP_047281610.1:p.Ser237Pro, XP_047281611.1:p.Ser183Pro, XP_047281617.1:p.Ser79Pro, XP_047281614.1:p.Ser237Pro

                                        20.

                                        rs1418885445 [Homo sapiens]
                                          Variant type:
                                          DEL
                                          Alleles:
                                          CA>- [Show Flanks]
                                          Chromosome:
                                          10:112445182 (GRCh38)
                                          10:114204940 (GRCh37)
                                          Canonical SPDI:
                                          NC_000010.11:112445181:CA:
                                          Gene:
                                          ZDHHC6 (Varview), VTI1A (Varview)
                                          Functional Consequence:
                                          non_coding_transcript_variant,upstream_transcript_variant,2KB_upstream_variant,genic_upstream_transcript_variant,frameshift_variant,coding_sequence_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          -=0./0 (ALFA)
                                          -=0.000008/2 (TOPMED)
                                          -=0.000036/5 (GnomAD)
                                          HGVS:
                                          NC_000010.11:g.112445182_112445183del, NC_000010.10:g.114204940_114204941del, XM_006717949.5:c.254_255del, XM_006717949.4:c.254_255del, XM_006717949.3:c.254_255del, XM_006717949.2:c.254_255del, XM_006717949.1:c.254_255del, XM_011540095.4:c.34_35del, XM_011540095.3:c.34_35del, XM_011540095.2:c.34_35del, XM_011540095.1:c.34_35del, XM_017016564.3:c.254_255del, XM_017016564.2:c.254_255del, XM_017016564.1:c.254_255del, XM_011540091.3:c.254_255del, XM_011540091.2:c.254_255del, XM_011540091.1:c.254_255del, XM_017016566.3:c.254_255del, XM_017016566.2:c.254_255del, XM_017016566.1:c.254_255del, NM_001351082.3:c.254_255del, NM_001351082.2:c.254_255del, NM_001351082.1:c.254_255del, XM_017016562.3:c.254_255del, XM_017016562.2:c.254_255del, XM_017016562.1:c.254_255del, XM_011540093.3:c.34_35del, XM_011540093.2:c.34_35del, XM_011540093.1:c.34_35del, NM_022494.3:c.254_255del, NM_022494.2:c.254_255del, NM_022494.1:c.254_255del, XM_017016563.3:c.254_255del, XM_017016563.2:c.254_255del, XM_017016563.1:c.254_255del, XM_017016568.3:c.34_35del, XM_017016568.2:c.34_35del, XM_017016568.1:c.34_35del, XM_017016567.3:c.254_255del, XM_017016567.2:c.254_255del, XM_017016567.1:c.254_255del, NM_001363544.2:c.254_255del, NM_001363544.1:c.254_255del, NM_001351084.2:c.254_255del, NM_001351084.1:c.254_255del, NR_147045.2:n.678_679del, NR_147045.1:n.723_724del, NM_001303134.2:c.254_255del, NM_001303134.1:c.254_255del, NM_001351083.2:c.254_255del, NM_001351083.1:c.254_255del, NM_001351085.2:c.34_35del, NM_001351085.1:c.34_35del, NM_001351086.2:c.34_35del, NM_001351086.1:c.34_35del, XM_047425657.1:c.254_255del, XR_007061983.1:n.678_679del, XM_047425653.1:c.254_255del, XM_047425660.1:c.34_35del, XM_047425659.1:c.34_35del, XM_047425656.1:c.254_255del, NM_001411066.1:c.254_255del, XM_047425654.1:c.254_255del, XM_047425655.1:c.254_255del, XM_047425661.1:c.34_35del, XM_047425658.1:c.254_255del, XP_006718012.1:p.Leu85fs, XP_011538397.1:p.Trp12fs, XP_016872053.1:p.Leu85fs, XP_011538393.1:p.Leu85fs, XP_016872055.1:p.Leu85fs, NP_001338011.1:p.Leu85fs, XP_016872051.1:p.Leu85fs, XP_011538395.1:p.Trp12fs, NP_071939.1:p.Leu85fs, XP_016872052.1:p.Leu85fs, XP_016872057.1:p.Trp12fs, XP_016872056.1:p.Leu85fs, NP_001350473.1:p.Leu85fs, NP_001338013.1:p.Leu85fs, NP_001290063.1:p.Leu85fs, NP_001338012.1:p.Leu85fs, NP_001338014.1:p.Trp12fs, NP_001338015.1:p.Trp12fs, XP_047281613.1:p.Leu85fs, XP_047281609.1:p.Leu85fs, XP_047281616.1:p.Trp12fs, XP_047281615.1:p.Trp12fs, XP_047281612.1:p.Leu85fs, XP_047281610.1:p.Leu85fs, XP_047281611.1:p.Leu85fs, XP_047281617.1:p.Trp12fs, XP_047281614.1:p.Leu85fs

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