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Items: 1 to 20 of 397

1.

rs1490018204 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>A [Show Flanks]
    Chromosome:
    16:58504616 (GRCh38)
    16:58538520 (GRCh37)
    Canonical SPDI:
    NC_000016.10:58504615:G:A
    Gene:
    NDRG4 (Varview)
    Functional Consequence:
    coding_sequence_variant,non_coding_transcript_variant,synonymous_variant
    Validated:
    by frequency
    MAF:
    A=0.000004/1 (GnomAD_exomes)
    HGVS:
    NC_000016.10:g.58504616G>A, NC_000016.9:g.58538520G>A, NG_041803.1:g.45972G>A, NM_022910.4:c.435G>A, NM_022910.3:c.435G>A, NM_020465.4:c.435G>A, NM_020465.3:c.435G>A, NM_001363869.2:c.174G>A, NM_001363869.1:c.174G>A, NM_001130487.2:c.495G>A, NM_001130487.1:c.495G>A, NR_040072.2:n.537G>A, NR_040072.1:n.537G>A, NM_001242833.2:c.429G>A, NM_001242833.1:c.429G>A, NM_001242834.2:c.393G>A, NM_001242834.1:c.393G>A, NM_001242835.2:c.339G>A, NM_001242835.1:c.339G>A, NM_001242836.2:c.339G>A, NM_001242836.1:c.339G>A, NM_001378340.1:c.525G>A, NM_001378332.1:c.585G>A, NM_001378333.1:c.549G>A, NM_001378334.1:c.585G>A, NM_001378335.1:c.549G>A, NM_001378336.1:c.495G>A, NM_001378337.1:c.528G>A, NM_001378338.1:c.489G>A, NM_001378339.1:c.525G>A, NM_001378341.1:c.474G>A, NM_001378342.1:c.489G>A, NM_001378346.1:c.435G>A, NM_001378343.1:c.474G>A, NM_001378345.1:c.435G>A, NM_001378344.1:c.429G>A, NM_001378347.1:c.393G>A, XM_011523290.4:c.525G>A, XM_011523290.3:c.525G>A, XM_011523290.2:c.525G>A, XM_011523290.1:c.525G>A, XM_011523291.4:c.489G>A, XM_011523291.3:c.489G>A, XM_011523291.2:c.489G>A, XM_011523291.1:c.489G>A, XM_006721253.4:c.564G>A, XM_006721253.3:c.564G>A, XM_006721253.2:c.564G>A, XM_006721253.1:c.564G>A, XM_006721256.4:c.525G>A, XM_006721256.3:c.525G>A, XM_006721256.2:c.525G>A, XM_006721256.1:c.525G>A, XM_017023582.3:c.489G>A, XM_017023582.2:c.489G>A, XM_017023582.1:c.489G>A, XM_011523293.3:c.435G>A, XM_011523293.2:c.435G>A, XM_011523293.1:c.435G>A, XM_017023583.3:c.525G>A, XM_017023583.2:c.525G>A, XM_017023583.1:c.525G>A, XM_047434509.1:c.525G>A

    2.

    rs1481868754 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      C>G [Show Flanks]
      Chromosome:
      16:58506596 (GRCh38)
      16:58540500 (GRCh37)
      Canonical SPDI:
      NC_000016.10:58506595:C:G
      Gene:
      NDRG4 (Varview)
      Functional Consequence:
      coding_sequence_variant,synonymous_variant,non_coding_transcript_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      G=0./0 (ALFA)
      G=0.000007/1 (GnomAD)
      G=0.000008/2 (TOPMED)
      HGVS:
      NC_000016.10:g.58506596C>G, NC_000016.9:g.58540500C>G, NG_041803.1:g.47952C>G, NM_022910.4:c.594C>G, NM_022910.3:c.594C>G, NM_020465.4:c.594C>G, NM_020465.3:c.594C>G, NM_001363869.2:c.333C>G, NM_001363869.1:c.333C>G, NM_001130487.2:c.654C>G, NM_001130487.1:c.654C>G, NR_040072.2:n.696C>G, NR_040072.1:n.696C>G, NM_001242833.2:c.588C>G, NM_001242833.1:c.588C>G, NM_001242834.2:c.552C>G, NM_001242834.1:c.552C>G, NM_001242835.2:c.498C>G, NM_001242835.1:c.498C>G, NM_001242836.2:c.498C>G, NM_001242836.1:c.498C>G, NM_001378340.1:c.684C>G, NM_001378332.1:c.744C>G, NM_001378333.1:c.708C>G, NM_001378334.1:c.744C>G, NM_001378335.1:c.708C>G, NM_001378336.1:c.654C>G, NM_001378337.1:c.687C>G, NM_001378338.1:c.648C>G, NM_001378339.1:c.684C>G, NM_001378341.1:c.633C>G, NM_001378342.1:c.648C>G, NM_001378346.1:c.594C>G, NM_001378343.1:c.633C>G, NM_001378345.1:c.594C>G, NM_001378344.1:c.588C>G, NM_001378347.1:c.552C>G, XM_011523290.4:c.684C>G, XM_011523290.3:c.684C>G, XM_011523290.2:c.684C>G, XM_011523290.1:c.684C>G, XM_011523291.4:c.648C>G, XM_011523291.3:c.648C>G, XM_011523291.2:c.648C>G, XM_011523291.1:c.648C>G, XM_006721253.4:c.723C>G, XM_006721253.3:c.723C>G, XM_006721253.2:c.723C>G, XM_006721253.1:c.723C>G, XM_006721256.4:c.684C>G, XM_006721256.3:c.684C>G, XM_006721256.2:c.684C>G, XM_006721256.1:c.684C>G, XM_017023582.3:c.648C>G, XM_017023582.2:c.648C>G, XM_017023582.1:c.648C>G, XM_011523293.3:c.594C>G, XM_011523293.2:c.594C>G, XM_011523293.1:c.594C>G, XM_017023583.3:c.684C>G, XM_017023583.2:c.684C>G, XM_017023583.1:c.684C>G, XM_047434509.1:c.684C>G

      3.

      rs1481530584 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        A>G [Show Flanks]
        Chromosome:
        16:58511436 (GRCh38)
        16:58545340 (GRCh37)
        Canonical SPDI:
        NC_000016.10:58511435:A:G
        Gene:
        NDRG4 (Varview)
        Functional Consequence:
        coding_sequence_variant,missense_variant,intron_variant,non_coding_transcript_variant
        Validated:
        by frequency
        MAF:
        G=0.000004/1 (GnomAD_exomes)
        HGVS:
        NC_000016.10:g.58511436A>G, NC_000016.9:g.58545340A>G, NG_041803.1:g.52792A>G, NM_022910.4:c.976A>G, NM_022910.3:c.976A>G, NM_020465.4:c.976A>G, NM_020465.3:c.976A>G, NM_001363869.2:c.715A>G, NM_001363869.1:c.715A>G, NM_001130487.2:c.1036A>G, NM_001130487.1:c.1036A>G, NR_040072.2:n.1078A>G, NR_040072.1:n.1078A>G, NM_001242833.2:c.970A>G, NM_001242833.1:c.970A>G, NM_001242834.2:c.934A>G, NM_001242834.1:c.934A>G, NM_001242835.2:c.919A>G, NM_001242835.1:c.919A>G, NM_001242836.2:c.880A>G, NM_001242836.1:c.880A>G, NM_001378340.1:c.1066A>G, NM_001378332.1:c.1165A>G, NM_001378333.1:c.1129A>G, NM_001378334.1:c.1126A>G, NM_001378335.1:c.1090A>G, NM_001378336.1:c.1075A>G, NM_001378337.1:c.1069A>G, NM_001378338.1:c.1069A>G, NM_001378339.1:c.1066A>G, NM_001378341.1:c.1054A>G, NM_001378342.1:c.1030A>G, NM_001378346.1:c.976A>G, NM_001378343.1:c.1015A>G, NM_001378345.1:c.1015A>G, NM_001378344.1:c.1009A>G, NM_001378347.1:c.973A>G, XM_011523290.4:c.1105A>G, XM_011523290.3:c.1105A>G, XM_011523290.2:c.1105A>G, XM_011523290.1:c.1105A>G, XM_011523291.4:c.1069A>G, XM_011523291.3:c.1069A>G, XM_011523291.2:c.1069A>G, XM_011523291.1:c.1069A>G, XM_006721253.4:c.1144A>G, XM_006721253.3:c.1144A>G, XM_006721253.2:c.1144A>G, XM_006721253.1:c.1144A>G, XM_006721256.4:c.1105A>G, XM_006721256.3:c.1105A>G, XM_006721256.2:c.1105A>G, XM_006721256.1:c.1105A>G, XM_017023582.3:c.1030A>G, XM_017023582.2:c.1030A>G, XM_017023582.1:c.1030A>G, XM_011523293.3:c.1015A>G, XM_011523293.2:c.1015A>G, XM_011523293.1:c.1015A>G, XM_047434509.1:c.1105A>G, NP_075061.1:p.Met326Val, NP_065198.1:p.Met326Val, NP_001350798.1:p.Met239Val, NP_001123959.1:p.Met346Val, NP_001229762.1:p.Met324Val, NP_001229763.1:p.Met312Val, NP_001229764.1:p.Met307Val, NP_001229765.1:p.Met294Val, NP_001365269.1:p.Met356Val, NP_001365261.1:p.Met389Val, NP_001365262.1:p.Met377Val, NP_001365263.1:p.Met376Val, NP_001365264.1:p.Met364Val, NP_001365265.1:p.Met359Val, NP_001365266.1:p.Met357Val, NP_001365267.1:p.Met357Val, NP_001365268.1:p.Met356Val, NP_001365270.1:p.Met352Val, NP_001365271.1:p.Met344Val, NP_001365275.1:p.Met326Val, NP_001365272.1:p.Met339Val, NP_001365274.1:p.Met339Val, NP_001365273.1:p.Met337Val, NP_001365276.1:p.Met325Val, XP_011521592.1:p.Met369Val, XP_011521593.1:p.Met357Val, XP_006721316.1:p.Met382Val, XP_006721319.1:p.Met369Val, XP_016879071.1:p.Met344Val, XP_011521595.1:p.Met339Val, XP_047290465.1:p.Met369Val

        4.

        rs1477691616 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          T>G [Show Flanks]
          Chromosome:
          16:58494970 (GRCh38)
          16:58528874 (GRCh37)
          Canonical SPDI:
          NC_000016.10:58494969:T:G
          Gene:
          NDRG4 (Varview)
          Functional Consequence:
          coding_sequence_variant,missense_variant,5_prime_UTR_variant,genic_upstream_transcript_variant
          Validated:
          by frequency,by alfa
          MAF:
          G=0.000047/1 (ALFA)
          G=0.000008/2 (GnomAD_exomes)
          HGVS:
          NC_000016.10:g.58494970T>G, NC_000016.9:g.58528874T>G, NG_041803.1:g.36326T>G, NM_022910.4:c.79T>G, NM_022910.3:c.79T>G, NM_020465.4:c.79T>G, NM_020465.3:c.79T>G, NM_001363869.2:c.-275T>G, NM_001363869.1:c.-275T>G, NM_001130487.2:c.139T>G, NM_001130487.1:c.139T>G, NM_001378340.1:c.79T>G, NM_001378332.1:c.139T>G, NM_001378333.1:c.139T>G, NM_001378334.1:c.139T>G, NM_001378335.1:c.139T>G, NM_001378336.1:c.139T>G, NM_001378337.1:c.118T>G, NM_001378338.1:c.79T>G, NM_001378339.1:c.79T>G, NM_001378341.1:c.118T>G, NM_001378342.1:c.79T>G, NM_001378346.1:c.79T>G, NM_001378343.1:c.118T>G, NM_001378345.1:c.79T>G, XM_011523290.4:c.79T>G, XM_011523290.3:c.79T>G, XM_011523290.2:c.79T>G, XM_011523290.1:c.79T>G, XM_011523291.4:c.79T>G, XM_011523291.3:c.79T>G, XM_011523291.2:c.79T>G, XM_011523291.1:c.79T>G, XM_006721253.4:c.118T>G, XM_006721253.3:c.118T>G, XM_006721253.2:c.118T>G, XM_006721253.1:c.118T>G, XM_006721256.4:c.79T>G, XM_006721256.3:c.79T>G, XM_006721256.2:c.79T>G, XM_006721256.1:c.79T>G, XM_017023582.3:c.79T>G, XM_017023582.2:c.79T>G, XM_017023582.1:c.79T>G, XM_011523293.3:c.79T>G, XM_011523293.2:c.79T>G, XM_011523293.1:c.79T>G, XM_017023583.3:c.79T>G, XM_017023583.2:c.79T>G, XM_017023583.1:c.79T>G, XM_047434509.1:c.79T>G, NP_075061.1:p.Ser27Ala, NP_065198.1:p.Ser27Ala, NP_001123959.1:p.Ser47Ala, NP_001365269.1:p.Ser27Ala, NP_001365261.1:p.Ser47Ala, NP_001365262.1:p.Ser47Ala, NP_001365263.1:p.Ser47Ala, NP_001365264.1:p.Ser47Ala, NP_001365265.1:p.Ser47Ala, NP_001365266.1:p.Ser40Ala, NP_001365267.1:p.Ser27Ala, NP_001365268.1:p.Ser27Ala, NP_001365270.1:p.Ser40Ala, NP_001365271.1:p.Ser27Ala, NP_001365275.1:p.Ser27Ala, NP_001365272.1:p.Ser40Ala, NP_001365274.1:p.Ser27Ala, XP_011521592.1:p.Ser27Ala, XP_011521593.1:p.Ser27Ala, XP_006721316.1:p.Ser40Ala, XP_006721319.1:p.Ser27Ala, XP_016879071.1:p.Ser27Ala, XP_011521595.1:p.Ser27Ala, XP_016879072.1:p.Ser27Ala, XP_047290465.1:p.Ser27Ala

          5.

          rs1468311830 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            A>G [Show Flanks]
            Chromosome:
            16:58503886 (GRCh38)
            16:58537790 (GRCh37)
            Canonical SPDI:
            NC_000016.10:58503885:A:G
            Gene:
            NDRG4 (Varview)
            Functional Consequence:
            coding_sequence_variant,missense_variant,5_prime_UTR_variant,non_coding_transcript_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            G=0.000084/1 (ALFA)
            G=0.000007/1 (GnomAD)
            HGVS:
            NC_000016.10:g.58503886A>G, NC_000016.9:g.58537790A>G, NG_041803.1:g.45242A>G, NM_022910.4:c.206A>G, NM_022910.3:c.206A>G, NM_020465.4:c.206A>G, NM_020465.3:c.206A>G, NM_001363869.2:c.-56A>G, NM_001363869.1:c.-56A>G, NM_001130487.2:c.266A>G, NM_001130487.1:c.266A>G, NR_040072.2:n.308A>G, NR_040072.1:n.308A>G, NM_001242833.2:c.200A>G, NM_001242833.1:c.200A>G, NM_001242834.2:c.164A>G, NM_001242834.1:c.164A>G, NM_001242835.2:c.110A>G, NM_001242835.1:c.110A>G, NM_001242836.2:c.110A>G, NM_001242836.1:c.110A>G, NM_001378340.1:c.296A>G, NM_001378332.1:c.356A>G, NM_001378333.1:c.320A>G, NM_001378334.1:c.356A>G, NM_001378335.1:c.320A>G, NM_001378336.1:c.266A>G, NM_001378337.1:c.299A>G, NM_001378338.1:c.260A>G, NM_001378339.1:c.296A>G, NM_001378341.1:c.245A>G, NM_001378342.1:c.260A>G, NM_001378346.1:c.206A>G, NM_001378343.1:c.245A>G, NM_001378345.1:c.206A>G, NM_001378344.1:c.200A>G, NM_001378347.1:c.164A>G, XM_011523290.4:c.296A>G, XM_011523290.3:c.296A>G, XM_011523290.2:c.296A>G, XM_011523290.1:c.296A>G, XM_011523291.4:c.260A>G, XM_011523291.3:c.260A>G, XM_011523291.2:c.260A>G, XM_011523291.1:c.260A>G, XM_006721253.4:c.335A>G, XM_006721253.3:c.335A>G, XM_006721253.2:c.335A>G, XM_006721253.1:c.335A>G, XM_006721256.4:c.296A>G, XM_006721256.3:c.296A>G, XM_006721256.2:c.296A>G, XM_006721256.1:c.296A>G, XM_017023582.3:c.260A>G, XM_017023582.2:c.260A>G, XM_017023582.1:c.260A>G, XM_011523293.3:c.206A>G, XM_011523293.2:c.206A>G, XM_011523293.1:c.206A>G, XM_017023583.3:c.296A>G, XM_017023583.2:c.296A>G, XM_017023583.1:c.296A>G, XM_047434509.1:c.296A>G, NP_075061.1:p.His69Arg, NP_065198.1:p.His69Arg, NP_001123959.1:p.His89Arg, NP_001229762.1:p.His67Arg, NP_001229763.1:p.His55Arg, NP_001229764.1:p.His37Arg, NP_001229765.1:p.His37Arg, NP_001365269.1:p.His99Arg, NP_001365261.1:p.His119Arg, NP_001365262.1:p.His107Arg, NP_001365263.1:p.His119Arg, NP_001365264.1:p.His107Arg, NP_001365265.1:p.His89Arg, NP_001365266.1:p.His100Arg, NP_001365267.1:p.His87Arg, NP_001365268.1:p.His99Arg, NP_001365270.1:p.His82Arg, NP_001365271.1:p.His87Arg, NP_001365275.1:p.His69Arg, NP_001365272.1:p.His82Arg, NP_001365274.1:p.His69Arg, NP_001365273.1:p.His67Arg, NP_001365276.1:p.His55Arg, XP_011521592.1:p.His99Arg, XP_011521593.1:p.His87Arg, XP_006721316.1:p.His112Arg, XP_006721319.1:p.His99Arg, XP_016879071.1:p.His87Arg, XP_011521595.1:p.His69Arg, XP_016879072.1:p.His99Arg, XP_047290465.1:p.His99Arg

            6.

            rs1466242306 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              C>T [Show Flanks]
              Chromosome:
              16:58503816 (GRCh38)
              16:58537720 (GRCh37)
              Canonical SPDI:
              NC_000016.10:58503815:C:T
              Gene:
              NDRG4 (Varview)
              Functional Consequence:
              5_prime_UTR_variant,non_coding_transcript_variant,missense_variant,coding_sequence_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              T=0./0 (ALFA)
              T=0.000004/1 (TOPMED)
              T=0.000007/1 (GnomAD)
              HGVS:
              NC_000016.10:g.58503816C>T, NC_000016.9:g.58537720C>T, NG_041803.1:g.45172C>T, NM_022910.4:c.136C>T, NM_022910.3:c.136C>T, NM_020465.4:c.136C>T, NM_020465.3:c.136C>T, NM_001363869.2:c.-126C>T, NM_001363869.1:c.-126C>T, NM_001130487.2:c.196C>T, NM_001130487.1:c.196C>T, NR_040072.2:n.238C>T, NR_040072.1:n.238C>T, NM_001242833.2:c.130C>T, NM_001242833.1:c.130C>T, NM_001242834.2:c.94C>T, NM_001242834.1:c.94C>T, NM_001242835.2:c.40C>T, NM_001242835.1:c.40C>T, NM_001242836.2:c.40C>T, NM_001242836.1:c.40C>T, NM_001378340.1:c.226C>T, NM_001378332.1:c.286C>T, NM_001378333.1:c.250C>T, NM_001378334.1:c.286C>T, NM_001378335.1:c.250C>T, NM_001378336.1:c.196C>T, NM_001378337.1:c.229C>T, NM_001378338.1:c.190C>T, NM_001378339.1:c.226C>T, NM_001378341.1:c.175C>T, NM_001378342.1:c.190C>T, NM_001378346.1:c.136C>T, NM_001378343.1:c.175C>T, NM_001378345.1:c.136C>T, NM_001378344.1:c.130C>T, NM_001378347.1:c.94C>T, XM_011523290.4:c.226C>T, XM_011523290.3:c.226C>T, XM_011523290.2:c.226C>T, XM_011523290.1:c.226C>T, XM_011523291.4:c.190C>T, XM_011523291.3:c.190C>T, XM_011523291.2:c.190C>T, XM_011523291.1:c.190C>T, XM_006721253.4:c.265C>T, XM_006721253.3:c.265C>T, XM_006721253.2:c.265C>T, XM_006721253.1:c.265C>T, XM_006721256.4:c.226C>T, XM_006721256.3:c.226C>T, XM_006721256.2:c.226C>T, XM_006721256.1:c.226C>T, XM_017023582.3:c.190C>T, XM_017023582.2:c.190C>T, XM_017023582.1:c.190C>T, XM_011523293.3:c.136C>T, XM_011523293.2:c.136C>T, XM_011523293.1:c.136C>T, XM_017023583.3:c.226C>T, XM_017023583.2:c.226C>T, XM_017023583.1:c.226C>T, XM_047434509.1:c.226C>T, NP_075061.1:p.Pro46Ser, NP_065198.1:p.Pro46Ser, NP_001123959.1:p.Pro66Ser, NP_001229762.1:p.Pro44Ser, NP_001229763.1:p.Pro32Ser, NP_001229764.1:p.Pro14Ser, NP_001229765.1:p.Pro14Ser, NP_001365269.1:p.Pro76Ser, NP_001365261.1:p.Pro96Ser, NP_001365262.1:p.Pro84Ser, NP_001365263.1:p.Pro96Ser, NP_001365264.1:p.Pro84Ser, NP_001365265.1:p.Pro66Ser, NP_001365266.1:p.Pro77Ser, NP_001365267.1:p.Pro64Ser, NP_001365268.1:p.Pro76Ser, NP_001365270.1:p.Pro59Ser, NP_001365271.1:p.Pro64Ser, NP_001365275.1:p.Pro46Ser, NP_001365272.1:p.Pro59Ser, NP_001365274.1:p.Pro46Ser, NP_001365273.1:p.Pro44Ser, NP_001365276.1:p.Pro32Ser, XP_011521592.1:p.Pro76Ser, XP_011521593.1:p.Pro64Ser, XP_006721316.1:p.Pro89Ser, XP_006721319.1:p.Pro76Ser, XP_016879071.1:p.Pro64Ser, XP_011521595.1:p.Pro46Ser, XP_016879072.1:p.Pro76Ser, XP_047290465.1:p.Pro76Ser

              7.

              rs1464855549 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                G>A [Show Flanks]
                Chromosome:
                16:58487811 (GRCh38)
                16:58521715 (GRCh37)
                Canonical SPDI:
                NC_000016.10:58487810:G:A
                Gene:
                NDRG4 (Varview)
                Functional Consequence:
                5_prime_UTR_variant,genic_upstream_transcript_variant,synonymous_variant,coding_sequence_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                A=0.000071/1 (ALFA)
                A=0.000014/2 (GnomAD_exomes)
                A=0.000019/5 (TOPMED)
                HGVS:
                NC_000016.10:g.58487811G>A, NC_000016.9:g.58521715G>A, NG_041803.1:g.29167G>A, NM_022910.4:c.33G>A, NM_022910.3:c.33G>A, NM_020465.4:c.33G>A, NM_020465.3:c.33G>A, NM_001363869.2:c.-321G>A, NM_001363869.1:c.-321G>A, NM_001130487.2:c.93G>A, NM_001130487.1:c.93G>A, NM_001378340.1:c.33G>A, NM_001378332.1:c.93G>A, NM_001378333.1:c.93G>A, NM_001378334.1:c.93G>A, NM_001378335.1:c.93G>A, NM_001378336.1:c.93G>A, NM_001378337.1:c.72G>A, NM_001378338.1:c.33G>A, NM_001378339.1:c.33G>A, NM_001378341.1:c.72G>A, NM_001378342.1:c.33G>A, NM_001378346.1:c.33G>A, NM_001378343.1:c.72G>A, NM_001378345.1:c.33G>A, XM_011523290.4:c.33G>A, XM_011523290.3:c.33G>A, XM_011523290.2:c.33G>A, XM_011523290.1:c.33G>A, XM_011523291.4:c.33G>A, XM_011523291.3:c.33G>A, XM_011523291.2:c.33G>A, XM_011523291.1:c.33G>A, XM_006721253.4:c.72G>A, XM_006721253.3:c.72G>A, XM_006721253.2:c.72G>A, XM_006721253.1:c.72G>A, XM_006721256.4:c.33G>A, XM_006721256.3:c.33G>A, XM_006721256.2:c.33G>A, XM_006721256.1:c.33G>A, XM_017023582.3:c.33G>A, XM_017023582.2:c.33G>A, XM_017023582.1:c.33G>A, XM_011523293.3:c.33G>A, XM_011523293.2:c.33G>A, XM_011523293.1:c.33G>A, XM_017023583.3:c.33G>A, XM_017023583.2:c.33G>A, XM_017023583.1:c.33G>A, XM_047434509.1:c.33G>A

                8.

                rs1454478285 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  C>G,T [Show Flanks]
                  Chromosome:
                  16:58487805 (GRCh38)
                  16:58521709 (GRCh37)
                  Canonical SPDI:
                  NC_000016.10:58487804:C:G,NC_000016.10:58487804:C:T
                  Gene:
                  NDRG4 (Varview)
                  Functional Consequence:
                  coding_sequence_variant,genic_upstream_transcript_variant,synonymous_variant,5_prime_UTR_variant,missense_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  T=0./0 (ALFA)
                  T=0.000004/1 (TOPMED)
                  HGVS:
                  NC_000016.10:g.58487805C>G, NC_000016.10:g.58487805C>T, NC_000016.9:g.58521709C>G, NC_000016.9:g.58521709C>T, NG_041803.1:g.29161C>G, NG_041803.1:g.29161C>T, NM_022910.4:c.27C>G, NM_022910.4:c.27C>T, NM_022910.3:c.27C>G, NM_022910.3:c.27C>T, NM_020465.4:c.27C>G, NM_020465.4:c.27C>T, NM_020465.3:c.27C>G, NM_020465.3:c.27C>T, NM_001363869.2:c.-327C>G, NM_001363869.2:c.-327C>T, NM_001363869.1:c.-327C>G, NM_001363869.1:c.-327C>T, NM_001130487.2:c.87C>G, NM_001130487.2:c.87C>T, NM_001130487.1:c.87C>G, NM_001130487.1:c.87C>T, NM_001378340.1:c.27C>G, NM_001378340.1:c.27C>T, NM_001378332.1:c.87C>G, NM_001378332.1:c.87C>T, NM_001378333.1:c.87C>G, NM_001378333.1:c.87C>T, NM_001378334.1:c.87C>G, NM_001378334.1:c.87C>T, NM_001378335.1:c.87C>G, NM_001378335.1:c.87C>T, NM_001378336.1:c.87C>G, NM_001378336.1:c.87C>T, NM_001378337.1:c.66C>G, NM_001378337.1:c.66C>T, NM_001378338.1:c.27C>G, NM_001378338.1:c.27C>T, NM_001378339.1:c.27C>G, NM_001378339.1:c.27C>T, NM_001378341.1:c.66C>G, NM_001378341.1:c.66C>T, NM_001378342.1:c.27C>G, NM_001378342.1:c.27C>T, NM_001378346.1:c.27C>G, NM_001378346.1:c.27C>T, NM_001378343.1:c.66C>G, NM_001378343.1:c.66C>T, NM_001378345.1:c.27C>G, NM_001378345.1:c.27C>T, XM_011523290.4:c.27C>G, XM_011523290.4:c.27C>T, XM_011523290.3:c.27C>G, XM_011523290.3:c.27C>T, XM_011523290.2:c.27C>G, XM_011523290.2:c.27C>T, XM_011523290.1:c.27C>G, XM_011523290.1:c.27C>T, XM_011523291.4:c.27C>G, XM_011523291.4:c.27C>T, XM_011523291.3:c.27C>G, XM_011523291.3:c.27C>T, XM_011523291.2:c.27C>G, XM_011523291.2:c.27C>T, XM_011523291.1:c.27C>G, XM_011523291.1:c.27C>T, XM_006721253.4:c.66C>G, XM_006721253.4:c.66C>T, XM_006721253.3:c.66C>G, XM_006721253.3:c.66C>T, XM_006721253.2:c.66C>G, XM_006721253.2:c.66C>T, XM_006721253.1:c.66C>G, XM_006721253.1:c.66C>T, XM_006721256.4:c.27C>G, XM_006721256.4:c.27C>T, XM_006721256.3:c.27C>G, XM_006721256.3:c.27C>T, XM_006721256.2:c.27C>G, XM_006721256.2:c.27C>T, XM_006721256.1:c.27C>G, XM_006721256.1:c.27C>T, XM_017023582.3:c.27C>G, XM_017023582.3:c.27C>T, XM_017023582.2:c.27C>G, XM_017023582.2:c.27C>T, XM_017023582.1:c.27C>G, XM_017023582.1:c.27C>T, XM_011523293.3:c.27C>G, XM_011523293.3:c.27C>T, XM_011523293.2:c.27C>G, XM_011523293.2:c.27C>T, XM_011523293.1:c.27C>G, XM_011523293.1:c.27C>T, XM_017023583.3:c.27C>G, XM_017023583.3:c.27C>T, XM_017023583.2:c.27C>G, XM_017023583.2:c.27C>T, XM_017023583.1:c.27C>G, XM_017023583.1:c.27C>T, XM_047434509.1:c.27C>G, XM_047434509.1:c.27C>T, NP_075061.1:p.Phe9Leu, NP_065198.1:p.Phe9Leu, NP_001123959.1:p.Phe29Leu, NP_001365269.1:p.Phe9Leu, NP_001365261.1:p.Phe29Leu, NP_001365262.1:p.Phe29Leu, NP_001365263.1:p.Phe29Leu, NP_001365264.1:p.Phe29Leu, NP_001365265.1:p.Phe29Leu, NP_001365266.1:p.Phe22Leu, NP_001365267.1:p.Phe9Leu, NP_001365268.1:p.Phe9Leu, NP_001365270.1:p.Phe22Leu, NP_001365271.1:p.Phe9Leu, NP_001365275.1:p.Phe9Leu, NP_001365272.1:p.Phe22Leu, NP_001365274.1:p.Phe9Leu, XP_011521592.1:p.Phe9Leu, XP_011521593.1:p.Phe9Leu, XP_006721316.1:p.Phe22Leu, XP_006721319.1:p.Phe9Leu, XP_016879071.1:p.Phe9Leu, XP_011521595.1:p.Phe9Leu, XP_016879072.1:p.Phe9Leu, XP_047290465.1:p.Phe9Leu

                  9.

                  rs1454118235 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    G>C [Show Flanks]
                    Chromosome:
                    16:58504218 (GRCh38)
                    16:58538122 (GRCh37)
                    Canonical SPDI:
                    NC_000016.10:58504217:G:C
                    Gene:
                    NDRG4 (Varview)
                    Functional Consequence:
                    non_coding_transcript_variant,synonymous_variant,coding_sequence_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    C=0./0 (ALFA)
                    C=0.000007/1 (GnomAD)
                    C=0.000008/2 (TOPMED)
                    HGVS:
                    NC_000016.10:g.58504218G>C, NC_000016.9:g.58538122G>C, NG_041803.1:g.45574G>C, NM_022910.4:c.288G>C, NM_022910.3:c.288G>C, NM_020465.4:c.288G>C, NM_020465.3:c.288G>C, NM_001363869.2:c.27G>C, NM_001363869.1:c.27G>C, NM_001130487.2:c.348G>C, NM_001130487.1:c.348G>C, NR_040072.2:n.390G>C, NR_040072.1:n.390G>C, NM_001242833.2:c.282G>C, NM_001242833.1:c.282G>C, NM_001242834.2:c.246G>C, NM_001242834.1:c.246G>C, NM_001242835.2:c.192G>C, NM_001242835.1:c.192G>C, NM_001242836.2:c.192G>C, NM_001242836.1:c.192G>C, NM_001378340.1:c.378G>C, NM_001378332.1:c.438G>C, NM_001378333.1:c.402G>C, NM_001378334.1:c.438G>C, NM_001378335.1:c.402G>C, NM_001378336.1:c.348G>C, NM_001378337.1:c.381G>C, NM_001378338.1:c.342G>C, NM_001378339.1:c.378G>C, NM_001378341.1:c.327G>C, NM_001378342.1:c.342G>C, NM_001378346.1:c.288G>C, NM_001378343.1:c.327G>C, NM_001378345.1:c.288G>C, NM_001378344.1:c.282G>C, NM_001378347.1:c.246G>C, XM_011523290.4:c.378G>C, XM_011523290.3:c.378G>C, XM_011523290.2:c.378G>C, XM_011523290.1:c.378G>C, XM_011523291.4:c.342G>C, XM_011523291.3:c.342G>C, XM_011523291.2:c.342G>C, XM_011523291.1:c.342G>C, XM_006721253.4:c.417G>C, XM_006721253.3:c.417G>C, XM_006721253.2:c.417G>C, XM_006721253.1:c.417G>C, XM_006721256.4:c.378G>C, XM_006721256.3:c.378G>C, XM_006721256.2:c.378G>C, XM_006721256.1:c.378G>C, XM_017023582.3:c.342G>C, XM_017023582.2:c.342G>C, XM_017023582.1:c.342G>C, XM_011523293.3:c.288G>C, XM_011523293.2:c.288G>C, XM_011523293.1:c.288G>C, XM_017023583.3:c.378G>C, XM_017023583.2:c.378G>C, XM_017023583.1:c.378G>C, XM_047434509.1:c.378G>C

                    10.

                    rs1453260811 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      A>C [Show Flanks]
                      Chromosome:
                      16:58511576 (GRCh38)
                      16:58545480 (GRCh37)
                      Canonical SPDI:
                      NC_000016.10:58511575:A:C
                      Gene:
                      NDRG4 (Varview)
                      Functional Consequence:
                      intron_variant,terminator_codon_variant,non_coding_transcript_variant,stop_lost
                      Validated:
                      by frequency,by alfa
                      MAF:
                      C=0./0 (ALFA)
                      C=0.000008/2 (TOPMED)
                      HGVS:
                      NC_000016.10:g.58511576A>C, NC_000016.9:g.58545480A>C, NG_041803.1:g.52932A>C, NM_022910.4:c.1116A>C, NM_022910.3:c.1116A>C, NM_020465.4:c.1116A>C, NM_020465.3:c.1116A>C, NM_001363869.2:c.855A>C, NM_001363869.1:c.855A>C, NM_001130487.2:c.1176A>C, NM_001130487.1:c.1176A>C, NR_040072.2:n.1218A>C, NR_040072.1:n.1218A>C, NM_001242833.2:c.1110A>C, NM_001242833.1:c.1110A>C, NM_001242834.2:c.1074A>C, NM_001242834.1:c.1074A>C, NM_001242835.2:c.1059A>C, NM_001242835.1:c.1059A>C, NM_001242836.2:c.1020A>C, NM_001242836.1:c.1020A>C, NM_001378340.1:c.1206A>C, NM_001378332.1:c.1305A>C, NM_001378333.1:c.1269A>C, NM_001378334.1:c.1266A>C, NM_001378335.1:c.1230A>C, NM_001378336.1:c.1215A>C, NM_001378337.1:c.1209A>C, NM_001378338.1:c.1209A>C, NM_001378339.1:c.1206A>C, NM_001378341.1:c.1194A>C, NM_001378342.1:c.1170A>C, NM_001378346.1:c.1116A>C, NM_001378343.1:c.1155A>C, NM_001378345.1:c.1155A>C, NM_001378344.1:c.1149A>C, NM_001378347.1:c.1113A>C, XM_011523290.4:c.1245A>C, XM_011523290.3:c.1245A>C, XM_011523290.2:c.1245A>C, XM_011523290.1:c.1245A>C, XM_011523291.4:c.1209A>C, XM_011523291.3:c.1209A>C, XM_011523291.2:c.1209A>C, XM_011523291.1:c.1209A>C, XM_006721253.4:c.1284A>C, XM_006721253.3:c.1284A>C, XM_006721253.2:c.1284A>C, XM_006721253.1:c.1284A>C, XM_006721256.4:c.1245A>C, XM_006721256.3:c.1245A>C, XM_006721256.2:c.1245A>C, XM_006721256.1:c.1245A>C, XM_017023582.3:c.1170A>C, XM_017023582.2:c.1170A>C, XM_017023582.1:c.1170A>C, XM_011523293.3:c.1155A>C, XM_011523293.2:c.1155A>C, XM_011523293.1:c.1155A>C, XM_047434509.1:c.1245A>C, NP_075061.1:p.Ter372Cys, NP_065198.1:p.Ter372Cys, NP_001350798.1:p.Ter285Cys, NP_001123959.1:p.Ter392Cys, NP_001229762.1:p.Ter370Cys, NP_001229763.1:p.Ter358Cys, NP_001229764.1:p.Ter353Cys, NP_001229765.1:p.Ter340Cys, NP_001365269.1:p.Ter402Cys, NP_001365261.1:p.Ter435Cys, NP_001365262.1:p.Ter423Cys, NP_001365263.1:p.Ter422Cys, NP_001365264.1:p.Ter410Cys, NP_001365265.1:p.Ter405Cys, NP_001365266.1:p.Ter403Cys, NP_001365267.1:p.Ter403Cys, NP_001365268.1:p.Ter402Cys, NP_001365270.1:p.Ter398Cys, NP_001365271.1:p.Ter390Cys, NP_001365275.1:p.Ter372Cys, NP_001365272.1:p.Ter385Cys, NP_001365274.1:p.Ter385Cys, NP_001365273.1:p.Ter383Cys, NP_001365276.1:p.Ter371Cys, XP_011521592.1:p.Ter415Cys, XP_011521593.1:p.Ter403Cys, XP_006721316.1:p.Ter428Cys, XP_006721319.1:p.Ter415Cys, XP_016879071.1:p.Ter390Cys, XP_011521595.1:p.Ter385Cys, XP_047290465.1:p.Ter415Cys

                      11.

                      rs1450932988 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        C>T [Show Flanks]
                        Chromosome:
                        16:58506918 (GRCh38)
                        16:58540822 (GRCh37)
                        Canonical SPDI:
                        NC_000016.10:58506917:C:T
                        Gene:
                        NDRG4 (Varview)
                        Functional Consequence:
                        non_coding_transcript_variant,synonymous_variant,coding_sequence_variant
                        Validated:
                        by frequency,by alfa
                        MAF:
                        T=0./0 (ALFA)
                        T=0.000008/2 (GnomAD_exomes)
                        HGVS:
                        NC_000016.10:g.58506918C>T, NC_000016.9:g.58540822C>T, NG_041803.1:g.48274C>T, NM_022910.4:c.619C>T, NM_022910.3:c.619C>T, NM_020465.4:c.619C>T, NM_020465.3:c.619C>T, NM_001363869.2:c.358C>T, NM_001363869.1:c.358C>T, NM_001130487.2:c.679C>T, NM_001130487.1:c.679C>T, NR_040072.2:n.721C>T, NR_040072.1:n.721C>T, NM_001242833.2:c.613C>T, NM_001242833.1:c.613C>T, NM_001242834.2:c.577C>T, NM_001242834.1:c.577C>T, NM_001242835.2:c.523C>T, NM_001242835.1:c.523C>T, NM_001242836.2:c.523C>T, NM_001242836.1:c.523C>T, NM_001378340.1:c.709C>T, NM_001378332.1:c.769C>T, NM_001378333.1:c.733C>T, NM_001378334.1:c.769C>T, NM_001378335.1:c.733C>T, NM_001378336.1:c.679C>T, NM_001378337.1:c.712C>T, NM_001378338.1:c.673C>T, NM_001378339.1:c.709C>T, NM_001378341.1:c.658C>T, NM_001378342.1:c.673C>T, NM_001378346.1:c.619C>T, NM_001378343.1:c.658C>T, NM_001378345.1:c.619C>T, NM_001378344.1:c.613C>T, NM_001378347.1:c.577C>T, XM_011523290.4:c.709C>T, XM_011523290.3:c.709C>T, XM_011523290.2:c.709C>T, XM_011523290.1:c.709C>T, XM_011523291.4:c.673C>T, XM_011523291.3:c.673C>T, XM_011523291.2:c.673C>T, XM_011523291.1:c.673C>T, XM_006721253.4:c.748C>T, XM_006721253.3:c.748C>T, XM_006721253.2:c.748C>T, XM_006721253.1:c.748C>T, XM_006721256.4:c.709C>T, XM_006721256.3:c.709C>T, XM_006721256.2:c.709C>T, XM_006721256.1:c.709C>T, XM_017023582.3:c.673C>T, XM_017023582.2:c.673C>T, XM_017023582.1:c.673C>T, XM_011523293.3:c.619C>T, XM_011523293.2:c.619C>T, XM_011523293.1:c.619C>T, XM_017023583.3:c.709C>T, XM_017023583.2:c.709C>T, XM_017023583.1:c.709C>T, XM_047434509.1:c.709C>T

                        12.

                        rs1447990565 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          C>T [Show Flanks]
                          Chromosome:
                          16:58507808 (GRCh38)
                          16:58541712 (GRCh37)
                          Canonical SPDI:
                          NC_000016.10:58507807:C:T
                          Gene:
                          NDRG4 (Varview)
                          Functional Consequence:
                          non_coding_transcript_variant,synonymous_variant,coding_sequence_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          T=0./0 (ALFA)
                          T=0.000007/1 (GnomAD)
                          T=0.000019/5 (TOPMED)
                          T=0.000028/7 (GnomAD_exomes)
                          HGVS:
                          NC_000016.10:g.58507808C>T, NC_000016.9:g.58541712C>T, NG_041803.1:g.49164C>T, NM_022910.4:c.717C>T, NM_022910.3:c.717C>T, NM_020465.4:c.717C>T, NM_020465.3:c.717C>T, NM_001363869.2:c.456C>T, NM_001363869.1:c.456C>T, NM_001130487.2:c.777C>T, NM_001130487.1:c.777C>T, NR_040072.2:n.819C>T, NR_040072.1:n.819C>T, NM_001242833.2:c.711C>T, NM_001242833.1:c.711C>T, NM_001242834.2:c.675C>T, NM_001242834.1:c.675C>T, NM_001242835.2:c.621C>T, NM_001242835.1:c.621C>T, NM_001242836.2:c.621C>T, NM_001242836.1:c.621C>T, NM_001378340.1:c.807C>T, NM_001378332.1:c.867C>T, NM_001378333.1:c.831C>T, NM_001378334.1:c.867C>T, NM_001378335.1:c.831C>T, NM_001378336.1:c.777C>T, NM_001378337.1:c.810C>T, NM_001378338.1:c.771C>T, NM_001378339.1:c.807C>T, NM_001378341.1:c.756C>T, NM_001378342.1:c.771C>T, NM_001378346.1:c.717C>T, NM_001378343.1:c.756C>T, NM_001378345.1:c.717C>T, NM_001378344.1:c.711C>T, NM_001378347.1:c.675C>T, XM_011523290.4:c.807C>T, XM_011523290.3:c.807C>T, XM_011523290.2:c.807C>T, XM_011523290.1:c.807C>T, XM_011523291.4:c.771C>T, XM_011523291.3:c.771C>T, XM_011523291.2:c.771C>T, XM_011523291.1:c.771C>T, XM_006721253.4:c.846C>T, XM_006721253.3:c.846C>T, XM_006721253.2:c.846C>T, XM_006721253.1:c.846C>T, XM_006721256.4:c.807C>T, XM_006721256.3:c.807C>T, XM_006721256.2:c.807C>T, XM_006721256.1:c.807C>T, XM_017023582.3:c.771C>T, XM_017023582.2:c.771C>T, XM_017023582.1:c.771C>T, XM_011523293.3:c.717C>T, XM_011523293.2:c.717C>T, XM_011523293.1:c.717C>T, XM_017023583.3:c.807C>T, XM_017023583.2:c.807C>T, XM_017023583.1:c.807C>T, XM_047434509.1:c.807C>T

                          13.

                          rs1447019463 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            G>A [Show Flanks]
                            Chromosome:
                            16:58507844 (GRCh38)
                            16:58541748 (GRCh37)
                            Canonical SPDI:
                            NC_000016.10:58507843:G:A
                            Gene:
                            NDRG4 (Varview)
                            Functional Consequence:
                            non_coding_transcript_variant,synonymous_variant,coding_sequence_variant
                            Validated:
                            by frequency
                            MAF:
                            A=0.000004/1 (GnomAD_exomes)
                            HGVS:
                            NC_000016.10:g.58507844G>A, NC_000016.9:g.58541748G>A, NG_041803.1:g.49200G>A, NM_022910.4:c.753G>A, NM_022910.3:c.753G>A, NM_020465.4:c.753G>A, NM_020465.3:c.753G>A, NM_001363869.2:c.492G>A, NM_001363869.1:c.492G>A, NM_001130487.2:c.813G>A, NM_001130487.1:c.813G>A, NR_040072.2:n.855G>A, NR_040072.1:n.855G>A, NM_001242833.2:c.747G>A, NM_001242833.1:c.747G>A, NM_001242834.2:c.711G>A, NM_001242834.1:c.711G>A, NM_001242835.2:c.657G>A, NM_001242835.1:c.657G>A, NM_001242836.2:c.657G>A, NM_001242836.1:c.657G>A, NM_001378340.1:c.843G>A, NM_001378332.1:c.903G>A, NM_001378333.1:c.867G>A, NM_001378334.1:c.903G>A, NM_001378335.1:c.867G>A, NM_001378336.1:c.813G>A, NM_001378337.1:c.846G>A, NM_001378338.1:c.807G>A, NM_001378339.1:c.843G>A, NM_001378341.1:c.792G>A, NM_001378342.1:c.807G>A, NM_001378346.1:c.753G>A, NM_001378343.1:c.792G>A, NM_001378345.1:c.753G>A, NM_001378344.1:c.747G>A, NM_001378347.1:c.711G>A, XM_011523290.4:c.843G>A, XM_011523290.3:c.843G>A, XM_011523290.2:c.843G>A, XM_011523290.1:c.843G>A, XM_011523291.4:c.807G>A, XM_011523291.3:c.807G>A, XM_011523291.2:c.807G>A, XM_011523291.1:c.807G>A, XM_006721253.4:c.882G>A, XM_006721253.3:c.882G>A, XM_006721253.2:c.882G>A, XM_006721253.1:c.882G>A, XM_006721256.4:c.843G>A, XM_006721256.3:c.843G>A, XM_006721256.2:c.843G>A, XM_006721256.1:c.843G>A, XM_017023582.3:c.807G>A, XM_017023582.2:c.807G>A, XM_017023582.1:c.807G>A, XM_011523293.3:c.753G>A, XM_011523293.2:c.753G>A, XM_011523293.1:c.753G>A, XM_017023583.3:c.843G>A, XM_017023583.2:c.843G>A, XM_017023583.1:c.843G>A, XM_047434509.1:c.843G>A

                            14.

                            rs1446571563 [Homo sapiens]
                              Variant type:
                              DELINS
                              Alleles:
                              ->G [Show Flanks]
                              Chromosome:
                              16:58507993 (GRCh38)
                              16:58541898 (GRCh37)
                              Canonical SPDI:
                              NC_000016.10:58507993:GGGG:GGGGG
                              Gene:
                              NDRG4 (Varview)
                              Functional Consequence:
                              non_coding_transcript_variant,frameshift_variant,coding_sequence_variant
                              Validated:
                              by frequency,by alfa
                              MAF:
                              GGGGG=0./0 (ALFA)
                              G=0.000004/1 (TOPMED)
                              HGVS:
                              NC_000016.10:g.58507997dup, NC_000016.9:g.58541901dup, NG_041803.1:g.49353dup, NM_022910.4:c.823dup, NM_022910.3:c.823dup, NM_020465.4:c.823dup, NM_020465.3:c.823dup, NM_001363869.2:c.562dup, NM_001363869.1:c.562dup, NM_001130487.2:c.883dup, NM_001130487.1:c.883dup, NR_040072.2:n.925dup, NR_040072.1:n.925dup, NM_001242833.2:c.817dup, NM_001242833.1:c.817dup, NM_001242834.2:c.781dup, NM_001242834.1:c.781dup, NM_001242835.2:c.727dup, NM_001242835.1:c.727dup, NM_001242836.2:c.727dup, NM_001242836.1:c.727dup, NM_001378340.1:c.913dup, NM_001378332.1:c.973dup, NM_001378333.1:c.937dup, NM_001378334.1:c.973dup, NM_001378335.1:c.937dup, NM_001378336.1:c.883dup, NM_001378337.1:c.916dup, NM_001378338.1:c.877dup, NM_001378339.1:c.913dup, NM_001378341.1:c.862dup, NM_001378342.1:c.877dup, NM_001378346.1:c.823dup, NM_001378343.1:c.862dup, NM_001378345.1:c.823dup, NM_001378344.1:c.817dup, NM_001378347.1:c.781dup, XM_011523290.4:c.913dup, XM_011523290.3:c.913dup, XM_011523290.2:c.913dup, XM_011523290.1:c.913dup, XM_011523291.4:c.877dup, XM_011523291.3:c.877dup, XM_011523291.2:c.877dup, XM_011523291.1:c.877dup, XM_006721253.4:c.952dup, XM_006721253.3:c.952dup, XM_006721253.2:c.952dup, XM_006721253.1:c.952dup, XM_006721256.4:c.913dup, XM_006721256.3:c.913dup, XM_006721256.2:c.913dup, XM_006721256.1:c.913dup, XM_017023582.3:c.877dup, XM_017023582.2:c.877dup, XM_017023582.1:c.877dup, XM_011523293.3:c.823dup, XM_011523293.2:c.823dup, XM_011523293.1:c.823dup, XM_017023583.3:c.913dup, XM_017023583.2:c.913dup, XM_017023583.1:c.913dup, XM_047434509.1:c.913dup, NP_075061.1:p.Val275fs, NP_065198.1:p.Val275fs, NP_001350798.1:p.Val188fs, NP_001123959.1:p.Val295fs, NP_001229762.1:p.Val273fs, NP_001229763.1:p.Val261fs, NP_001229764.1:p.Val243fs, NP_001229765.1:p.Val243fs, NP_001365269.1:p.Val305fs, NP_001365261.1:p.Val325fs, NP_001365262.1:p.Val313fs, NP_001365263.1:p.Val325fs, NP_001365264.1:p.Val313fs, NP_001365265.1:p.Val295fs, NP_001365266.1:p.Val306fs, NP_001365267.1:p.Val293fs, NP_001365268.1:p.Val305fs, NP_001365270.1:p.Val288fs, NP_001365271.1:p.Val293fs, NP_001365275.1:p.Val275fs, NP_001365272.1:p.Val288fs, NP_001365274.1:p.Val275fs, NP_001365273.1:p.Val273fs, NP_001365276.1:p.Val261fs, XP_011521592.1:p.Val305fs, XP_011521593.1:p.Val293fs, XP_006721316.1:p.Val318fs, XP_006721319.1:p.Val305fs, XP_016879071.1:p.Val293fs, XP_011521595.1:p.Val275fs, XP_016879072.1:p.Val305fs, XP_047290465.1:p.Val305fs

                              15.

                              rs1446171760 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                A>G [Show Flanks]
                                Chromosome:
                                16:58506976 (GRCh38)
                                16:58540880 (GRCh37)
                                Canonical SPDI:
                                NC_000016.10:58506975:A:G
                                Gene:
                                NDRG4 (Varview)
                                Functional Consequence:
                                non_coding_transcript_variant,missense_variant,coding_sequence_variant
                                Validated:
                                by frequency,by alfa
                                MAF:
                                G=0./0 (ALFA)
                                HGVS:
                                NC_000016.10:g.58506976A>G, NC_000016.9:g.58540880A>G, NG_041803.1:g.48332A>G, NM_022910.4:c.677A>G, NM_022910.3:c.677A>G, NM_020465.4:c.677A>G, NM_020465.3:c.677A>G, NM_001363869.2:c.416A>G, NM_001363869.1:c.416A>G, NM_001130487.2:c.737A>G, NM_001130487.1:c.737A>G, NR_040072.2:n.779A>G, NR_040072.1:n.779A>G, NM_001242833.2:c.671A>G, NM_001242833.1:c.671A>G, NM_001242834.2:c.635A>G, NM_001242834.1:c.635A>G, NM_001242835.2:c.581A>G, NM_001242835.1:c.581A>G, NM_001242836.2:c.581A>G, NM_001242836.1:c.581A>G, NM_001378340.1:c.767A>G, NM_001378332.1:c.827A>G, NM_001378333.1:c.791A>G, NM_001378334.1:c.827A>G, NM_001378335.1:c.791A>G, NM_001378336.1:c.737A>G, NM_001378337.1:c.770A>G, NM_001378338.1:c.731A>G, NM_001378339.1:c.767A>G, NM_001378341.1:c.716A>G, NM_001378342.1:c.731A>G, NM_001378346.1:c.677A>G, NM_001378343.1:c.716A>G, NM_001378345.1:c.677A>G, NM_001378344.1:c.671A>G, NM_001378347.1:c.635A>G, XM_011523290.4:c.767A>G, XM_011523290.3:c.767A>G, XM_011523290.2:c.767A>G, XM_011523290.1:c.767A>G, XM_011523291.4:c.731A>G, XM_011523291.3:c.731A>G, XM_011523291.2:c.731A>G, XM_011523291.1:c.731A>G, XM_006721253.4:c.806A>G, XM_006721253.3:c.806A>G, XM_006721253.2:c.806A>G, XM_006721253.1:c.806A>G, XM_006721256.4:c.767A>G, XM_006721256.3:c.767A>G, XM_006721256.2:c.767A>G, XM_006721256.1:c.767A>G, XM_017023582.3:c.731A>G, XM_017023582.2:c.731A>G, XM_017023582.1:c.731A>G, XM_011523293.3:c.677A>G, XM_011523293.2:c.677A>G, XM_011523293.1:c.677A>G, XM_017023583.3:c.767A>G, XM_017023583.2:c.767A>G, XM_017023583.1:c.767A>G, XM_047434509.1:c.767A>G, NP_075061.1:p.Asn226Ser, NP_065198.1:p.Asn226Ser, NP_001350798.1:p.Asn139Ser, NP_001123959.1:p.Asn246Ser, NP_001229762.1:p.Asn224Ser, NP_001229763.1:p.Asn212Ser, NP_001229764.1:p.Asn194Ser, NP_001229765.1:p.Asn194Ser, NP_001365269.1:p.Asn256Ser, NP_001365261.1:p.Asn276Ser, NP_001365262.1:p.Asn264Ser, NP_001365263.1:p.Asn276Ser, NP_001365264.1:p.Asn264Ser, NP_001365265.1:p.Asn246Ser, NP_001365266.1:p.Asn257Ser, NP_001365267.1:p.Asn244Ser, NP_001365268.1:p.Asn256Ser, NP_001365270.1:p.Asn239Ser, NP_001365271.1:p.Asn244Ser, NP_001365275.1:p.Asn226Ser, NP_001365272.1:p.Asn239Ser, NP_001365274.1:p.Asn226Ser, NP_001365273.1:p.Asn224Ser, NP_001365276.1:p.Asn212Ser, XP_011521592.1:p.Asn256Ser, XP_011521593.1:p.Asn244Ser, XP_006721316.1:p.Asn269Ser, XP_006721319.1:p.Asn256Ser, XP_016879071.1:p.Asn244Ser, XP_011521595.1:p.Asn226Ser, XP_016879072.1:p.Asn256Ser, XP_047290465.1:p.Asn256Ser

                                16.

                                rs1443666860 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  C>G [Show Flanks]
                                  Chromosome:
                                  16:58504384 (GRCh38)
                                  16:58538288 (GRCh37)
                                  Canonical SPDI:
                                  NC_000016.10:58504383:C:G
                                  Gene:
                                  NDRG4 (Varview)
                                  Functional Consequence:
                                  coding_sequence_variant,missense_variant,non_coding_transcript_variant
                                  Validated:
                                  by frequency,by alfa
                                  MAF:
                                  G=0./0 (ALFA)
                                  G=0.000004/1 (GnomAD_exomes)
                                  HGVS:
                                  NC_000016.10:g.58504384C>G, NC_000016.9:g.58538288C>G, NG_041803.1:g.45740C>G, NM_022910.4:c.370C>G, NM_022910.3:c.370C>G, NM_020465.4:c.370C>G, NM_020465.3:c.370C>G, NM_001363869.2:c.109C>G, NM_001363869.1:c.109C>G, NM_001130487.2:c.430C>G, NM_001130487.1:c.430C>G, NR_040072.2:n.472C>G, NR_040072.1:n.472C>G, NM_001242833.2:c.364C>G, NM_001242833.1:c.364C>G, NM_001242834.2:c.328C>G, NM_001242834.1:c.328C>G, NM_001242835.2:c.274C>G, NM_001242835.1:c.274C>G, NM_001242836.2:c.274C>G, NM_001242836.1:c.274C>G, NM_001378340.1:c.460C>G, NM_001378332.1:c.520C>G, NM_001378333.1:c.484C>G, NM_001378334.1:c.520C>G, NM_001378335.1:c.484C>G, NM_001378336.1:c.430C>G, NM_001378337.1:c.463C>G, NM_001378338.1:c.424C>G, NM_001378339.1:c.460C>G, NM_001378341.1:c.409C>G, NM_001378342.1:c.424C>G, NM_001378346.1:c.370C>G, NM_001378343.1:c.409C>G, NM_001378345.1:c.370C>G, NM_001378344.1:c.364C>G, NM_001378347.1:c.328C>G, XM_011523290.4:c.460C>G, XM_011523290.3:c.460C>G, XM_011523290.2:c.460C>G, XM_011523290.1:c.460C>G, XM_011523291.4:c.424C>G, XM_011523291.3:c.424C>G, XM_011523291.2:c.424C>G, XM_011523291.1:c.424C>G, XM_006721253.4:c.499C>G, XM_006721253.3:c.499C>G, XM_006721253.2:c.499C>G, XM_006721253.1:c.499C>G, XM_006721256.4:c.460C>G, XM_006721256.3:c.460C>G, XM_006721256.2:c.460C>G, XM_006721256.1:c.460C>G, XM_017023582.3:c.424C>G, XM_017023582.2:c.424C>G, XM_017023582.1:c.424C>G, XM_011523293.3:c.370C>G, XM_011523293.2:c.370C>G, XM_011523293.1:c.370C>G, XM_017023583.3:c.460C>G, XM_017023583.2:c.460C>G, XM_017023583.1:c.460C>G, XM_047434509.1:c.460C>G, NP_075061.1:p.Leu124Val, NP_065198.1:p.Leu124Val, NP_001350798.1:p.Leu37Val, NP_001123959.1:p.Leu144Val, NP_001229762.1:p.Leu122Val, NP_001229763.1:p.Leu110Val, NP_001229764.1:p.Leu92Val, NP_001229765.1:p.Leu92Val, NP_001365269.1:p.Leu154Val, NP_001365261.1:p.Leu174Val, NP_001365262.1:p.Leu162Val, NP_001365263.1:p.Leu174Val, NP_001365264.1:p.Leu162Val, NP_001365265.1:p.Leu144Val, NP_001365266.1:p.Leu155Val, NP_001365267.1:p.Leu142Val, NP_001365268.1:p.Leu154Val, NP_001365270.1:p.Leu137Val, NP_001365271.1:p.Leu142Val, NP_001365275.1:p.Leu124Val, NP_001365272.1:p.Leu137Val, NP_001365274.1:p.Leu124Val, NP_001365273.1:p.Leu122Val, NP_001365276.1:p.Leu110Val, XP_011521592.1:p.Leu154Val, XP_011521593.1:p.Leu142Val, XP_006721316.1:p.Leu167Val, XP_006721319.1:p.Leu154Val, XP_016879071.1:p.Leu142Val, XP_011521595.1:p.Leu124Val, XP_016879072.1:p.Leu154Val, XP_047290465.1:p.Leu154Val

                                  17.

                                  rs1442444709 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    G>T [Show Flanks]
                                    Chromosome:
                                    16:58504395 (GRCh38)
                                    16:58538299 (GRCh37)
                                    Canonical SPDI:
                                    NC_000016.10:58504394:G:T
                                    Gene:
                                    NDRG4 (Varview)
                                    Functional Consequence:
                                    coding_sequence_variant,missense_variant,non_coding_transcript_variant
                                    Validated:
                                    by frequency
                                    MAF:
                                    T=0.000004/1 (GnomAD_exomes)
                                    HGVS:
                                    NC_000016.10:g.58504395G>T, NC_000016.9:g.58538299G>T, NG_041803.1:g.45751G>T, NM_022910.4:c.381G>T, NM_022910.3:c.381G>T, NM_020465.4:c.381G>T, NM_020465.3:c.381G>T, NM_001363869.2:c.120G>T, NM_001363869.1:c.120G>T, NM_001130487.2:c.441G>T, NM_001130487.1:c.441G>T, NR_040072.2:n.483G>T, NR_040072.1:n.483G>T, NM_001242833.2:c.375G>T, NM_001242833.1:c.375G>T, NM_001242834.2:c.339G>T, NM_001242834.1:c.339G>T, NM_001242835.2:c.285G>T, NM_001242835.1:c.285G>T, NM_001242836.2:c.285G>T, NM_001242836.1:c.285G>T, NM_001378340.1:c.471G>T, NM_001378332.1:c.531G>T, NM_001378333.1:c.495G>T, NM_001378334.1:c.531G>T, NM_001378335.1:c.495G>T, NM_001378336.1:c.441G>T, NM_001378337.1:c.474G>T, NM_001378338.1:c.435G>T, NM_001378339.1:c.471G>T, NM_001378341.1:c.420G>T, NM_001378342.1:c.435G>T, NM_001378346.1:c.381G>T, NM_001378343.1:c.420G>T, NM_001378345.1:c.381G>T, NM_001378344.1:c.375G>T, NM_001378347.1:c.339G>T, XM_011523290.4:c.471G>T, XM_011523290.3:c.471G>T, XM_011523290.2:c.471G>T, XM_011523290.1:c.471G>T, XM_011523291.4:c.435G>T, XM_011523291.3:c.435G>T, XM_011523291.2:c.435G>T, XM_011523291.1:c.435G>T, XM_006721253.4:c.510G>T, XM_006721253.3:c.510G>T, XM_006721253.2:c.510G>T, XM_006721253.1:c.510G>T, XM_006721256.4:c.471G>T, XM_006721256.3:c.471G>T, XM_006721256.2:c.471G>T, XM_006721256.1:c.471G>T, XM_017023582.3:c.435G>T, XM_017023582.2:c.435G>T, XM_017023582.1:c.435G>T, XM_011523293.3:c.381G>T, XM_011523293.2:c.381G>T, XM_011523293.1:c.381G>T, XM_017023583.3:c.471G>T, XM_017023583.2:c.471G>T, XM_017023583.1:c.471G>T, XM_047434509.1:c.471G>T, NP_075061.1:p.Met127Ile, NP_065198.1:p.Met127Ile, NP_001350798.1:p.Met40Ile, NP_001123959.1:p.Met147Ile, NP_001229762.1:p.Met125Ile, NP_001229763.1:p.Met113Ile, NP_001229764.1:p.Met95Ile, NP_001229765.1:p.Met95Ile, NP_001365269.1:p.Met157Ile, NP_001365261.1:p.Met177Ile, NP_001365262.1:p.Met165Ile, NP_001365263.1:p.Met177Ile, NP_001365264.1:p.Met165Ile, NP_001365265.1:p.Met147Ile, NP_001365266.1:p.Met158Ile, NP_001365267.1:p.Met145Ile, NP_001365268.1:p.Met157Ile, NP_001365270.1:p.Met140Ile, NP_001365271.1:p.Met145Ile, NP_001365275.1:p.Met127Ile, NP_001365272.1:p.Met140Ile, NP_001365274.1:p.Met127Ile, NP_001365273.1:p.Met125Ile, NP_001365276.1:p.Met113Ile, XP_011521592.1:p.Met157Ile, XP_011521593.1:p.Met145Ile, XP_006721316.1:p.Met170Ile, XP_006721319.1:p.Met157Ile, XP_016879071.1:p.Met145Ile, XP_011521595.1:p.Met127Ile, XP_016879072.1:p.Met157Ile, XP_047290465.1:p.Met157Ile

                                    18.

                                    rs1441370270 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      G>A [Show Flanks]
                                      Chromosome:
                                      16:58507970 (GRCh38)
                                      16:58541874 (GRCh37)
                                      Canonical SPDI:
                                      NC_000016.10:58507969:G:A
                                      Gene:
                                      NDRG4 (Varview)
                                      Functional Consequence:
                                      coding_sequence_variant,missense_variant,non_coding_transcript_variant
                                      HGVS:
                                      NC_000016.10:g.58507970G>A, NC_000016.9:g.58541874G>A, NG_041803.1:g.49326G>A, NM_022910.4:c.796G>A, NM_022910.3:c.796G>A, NM_020465.4:c.796G>A, NM_020465.3:c.796G>A, NM_001363869.2:c.535G>A, NM_001363869.1:c.535G>A, NM_001130487.2:c.856G>A, NM_001130487.1:c.856G>A, NR_040072.2:n.898G>A, NR_040072.1:n.898G>A, NM_001242833.2:c.790G>A, NM_001242833.1:c.790G>A, NM_001242834.2:c.754G>A, NM_001242834.1:c.754G>A, NM_001242835.2:c.700G>A, NM_001242835.1:c.700G>A, NM_001242836.2:c.700G>A, NM_001242836.1:c.700G>A, NM_001378340.1:c.886G>A, NM_001378332.1:c.946G>A, NM_001378333.1:c.910G>A, NM_001378334.1:c.946G>A, NM_001378335.1:c.910G>A, NM_001378336.1:c.856G>A, NM_001378337.1:c.889G>A, NM_001378338.1:c.850G>A, NM_001378339.1:c.886G>A, NM_001378341.1:c.835G>A, NM_001378342.1:c.850G>A, NM_001378346.1:c.796G>A, NM_001378343.1:c.835G>A, NM_001378345.1:c.796G>A, NM_001378344.1:c.790G>A, NM_001378347.1:c.754G>A, XM_011523290.4:c.886G>A, XM_011523290.3:c.886G>A, XM_011523290.2:c.886G>A, XM_011523290.1:c.886G>A, XM_011523291.4:c.850G>A, XM_011523291.3:c.850G>A, XM_011523291.2:c.850G>A, XM_011523291.1:c.850G>A, XM_006721253.4:c.925G>A, XM_006721253.3:c.925G>A, XM_006721253.2:c.925G>A, XM_006721253.1:c.925G>A, XM_006721256.4:c.886G>A, XM_006721256.3:c.886G>A, XM_006721256.2:c.886G>A, XM_006721256.1:c.886G>A, XM_017023582.3:c.850G>A, XM_017023582.2:c.850G>A, XM_017023582.1:c.850G>A, XM_011523293.3:c.796G>A, XM_011523293.2:c.796G>A, XM_011523293.1:c.796G>A, XM_017023583.3:c.886G>A, XM_017023583.2:c.886G>A, XM_017023583.1:c.886G>A, XM_047434509.1:c.886G>A, NP_075061.1:p.Gly266Arg, NP_065198.1:p.Gly266Arg, NP_001350798.1:p.Gly179Arg, NP_001123959.1:p.Gly286Arg, NP_001229762.1:p.Gly264Arg, NP_001229763.1:p.Gly252Arg, NP_001229764.1:p.Gly234Arg, NP_001229765.1:p.Gly234Arg, NP_001365269.1:p.Gly296Arg, NP_001365261.1:p.Gly316Arg, NP_001365262.1:p.Gly304Arg, NP_001365263.1:p.Gly316Arg, NP_001365264.1:p.Gly304Arg, NP_001365265.1:p.Gly286Arg, NP_001365266.1:p.Gly297Arg, NP_001365267.1:p.Gly284Arg, NP_001365268.1:p.Gly296Arg, NP_001365270.1:p.Gly279Arg, NP_001365271.1:p.Gly284Arg, NP_001365275.1:p.Gly266Arg, NP_001365272.1:p.Gly279Arg, NP_001365274.1:p.Gly266Arg, NP_001365273.1:p.Gly264Arg, NP_001365276.1:p.Gly252Arg, XP_011521592.1:p.Gly296Arg, XP_011521593.1:p.Gly284Arg, XP_006721316.1:p.Gly309Arg, XP_006721319.1:p.Gly296Arg, XP_016879071.1:p.Gly284Arg, XP_011521595.1:p.Gly266Arg, XP_016879072.1:p.Gly296Arg, XP_047290465.1:p.Gly296Arg

                                      19.

                                      rs1438130542 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        A>C,G [Show Flanks]
                                        Chromosome:
                                        16:58504201 (GRCh38)
                                        16:58538105 (GRCh37)
                                        Canonical SPDI:
                                        NC_000016.10:58504200:A:C,NC_000016.10:58504200:A:G
                                        Gene:
                                        NDRG4 (Varview)
                                        Functional Consequence:
                                        coding_sequence_variant,missense_variant,non_coding_transcript_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        G=0./0 (ALFA)
                                        G=0.000007/1 (GnomAD)
                                        HGVS:
                                        NC_000016.10:g.58504201A>C, NC_000016.10:g.58504201A>G, NC_000016.9:g.58538105A>C, NC_000016.9:g.58538105A>G, NG_041803.1:g.45557A>C, NG_041803.1:g.45557A>G, NM_022910.4:c.271A>C, NM_022910.4:c.271A>G, NM_022910.3:c.271A>C, NM_022910.3:c.271A>G, NM_020465.4:c.271A>C, NM_020465.4:c.271A>G, NM_020465.3:c.271A>C, NM_020465.3:c.271A>G, NM_001363869.2:c.10A>C, NM_001363869.2:c.10A>G, NM_001363869.1:c.10A>C, NM_001363869.1:c.10A>G, NM_001130487.2:c.331A>C, NM_001130487.2:c.331A>G, NM_001130487.1:c.331A>C, NM_001130487.1:c.331A>G, NR_040072.2:n.373A>C, NR_040072.2:n.373A>G, NR_040072.1:n.373A>C, NR_040072.1:n.373A>G, NM_001242833.2:c.265A>C, NM_001242833.2:c.265A>G, NM_001242833.1:c.265A>C, NM_001242833.1:c.265A>G, NM_001242834.2:c.229A>C, NM_001242834.2:c.229A>G, NM_001242834.1:c.229A>C, NM_001242834.1:c.229A>G, NM_001242835.2:c.175A>C, NM_001242835.2:c.175A>G, NM_001242835.1:c.175A>C, NM_001242835.1:c.175A>G, NM_001242836.2:c.175A>C, NM_001242836.2:c.175A>G, NM_001242836.1:c.175A>C, NM_001242836.1:c.175A>G, NM_001378340.1:c.361A>C, NM_001378340.1:c.361A>G, NM_001378332.1:c.421A>C, NM_001378332.1:c.421A>G, NM_001378333.1:c.385A>C, NM_001378333.1:c.385A>G, NM_001378334.1:c.421A>C, NM_001378334.1:c.421A>G, NM_001378335.1:c.385A>C, NM_001378335.1:c.385A>G, NM_001378336.1:c.331A>C, NM_001378336.1:c.331A>G, NM_001378337.1:c.364A>C, NM_001378337.1:c.364A>G, NM_001378338.1:c.325A>C, NM_001378338.1:c.325A>G, NM_001378339.1:c.361A>C, NM_001378339.1:c.361A>G, NM_001378341.1:c.310A>C, NM_001378341.1:c.310A>G, NM_001378342.1:c.325A>C, NM_001378342.1:c.325A>G, NM_001378346.1:c.271A>C, NM_001378346.1:c.271A>G, NM_001378343.1:c.310A>C, NM_001378343.1:c.310A>G, NM_001378345.1:c.271A>C, NM_001378345.1:c.271A>G, NM_001378344.1:c.265A>C, NM_001378344.1:c.265A>G, NM_001378347.1:c.229A>C, NM_001378347.1:c.229A>G, XM_011523290.4:c.361A>C, XM_011523290.4:c.361A>G, XM_011523290.3:c.361A>C, XM_011523290.3:c.361A>G, XM_011523290.2:c.361A>C, XM_011523290.2:c.361A>G, XM_011523290.1:c.361A>C, XM_011523290.1:c.361A>G, XM_011523291.4:c.325A>C, XM_011523291.4:c.325A>G, XM_011523291.3:c.325A>C, XM_011523291.3:c.325A>G, XM_011523291.2:c.325A>C, XM_011523291.2:c.325A>G, XM_011523291.1:c.325A>C, XM_011523291.1:c.325A>G, XM_006721253.4:c.400A>C, XM_006721253.4:c.400A>G, XM_006721253.3:c.400A>C, XM_006721253.3:c.400A>G, XM_006721253.2:c.400A>C, XM_006721253.2:c.400A>G, XM_006721253.1:c.400A>C, XM_006721253.1:c.400A>G, XM_006721256.4:c.361A>C, XM_006721256.4:c.361A>G, XM_006721256.3:c.361A>C, XM_006721256.3:c.361A>G, XM_006721256.2:c.361A>C, XM_006721256.2:c.361A>G, XM_006721256.1:c.361A>C, XM_006721256.1:c.361A>G, XM_017023582.3:c.325A>C, XM_017023582.3:c.325A>G, XM_017023582.2:c.325A>C, XM_017023582.2:c.325A>G, XM_017023582.1:c.325A>C, XM_017023582.1:c.325A>G, XM_011523293.3:c.271A>C, XM_011523293.3:c.271A>G, XM_011523293.2:c.271A>C, XM_011523293.2:c.271A>G, XM_011523293.1:c.271A>C, XM_011523293.1:c.271A>G, XM_017023583.3:c.361A>C, XM_017023583.3:c.361A>G, XM_017023583.2:c.361A>C, XM_017023583.2:c.361A>G, XM_017023583.1:c.361A>C, XM_017023583.1:c.361A>G, XM_047434509.1:c.361A>C, XM_047434509.1:c.361A>G, NP_075061.1:p.Ile91Leu, NP_075061.1:p.Ile91Val, NP_065198.1:p.Ile91Leu, NP_065198.1:p.Ile91Val, NP_001350798.1:p.Ile4Leu, NP_001350798.1:p.Ile4Val, NP_001123959.1:p.Ile111Leu, NP_001123959.1:p.Ile111Val, NP_001229762.1:p.Ile89Leu, NP_001229762.1:p.Ile89Val, NP_001229763.1:p.Ile77Leu, NP_001229763.1:p.Ile77Val, NP_001229764.1:p.Ile59Leu, NP_001229764.1:p.Ile59Val, NP_001229765.1:p.Ile59Leu, NP_001229765.1:p.Ile59Val, NP_001365269.1:p.Ile121Leu, NP_001365269.1:p.Ile121Val, NP_001365261.1:p.Ile141Leu, NP_001365261.1:p.Ile141Val, NP_001365262.1:p.Ile129Leu, NP_001365262.1:p.Ile129Val, NP_001365263.1:p.Ile141Leu, NP_001365263.1:p.Ile141Val, NP_001365264.1:p.Ile129Leu, NP_001365264.1:p.Ile129Val, NP_001365265.1:p.Ile111Leu, NP_001365265.1:p.Ile111Val, NP_001365266.1:p.Ile122Leu, NP_001365266.1:p.Ile122Val, NP_001365267.1:p.Ile109Leu, NP_001365267.1:p.Ile109Val, NP_001365268.1:p.Ile121Leu, NP_001365268.1:p.Ile121Val, NP_001365270.1:p.Ile104Leu, NP_001365270.1:p.Ile104Val, NP_001365271.1:p.Ile109Leu, NP_001365271.1:p.Ile109Val, NP_001365275.1:p.Ile91Leu, NP_001365275.1:p.Ile91Val, NP_001365272.1:p.Ile104Leu, NP_001365272.1:p.Ile104Val, NP_001365274.1:p.Ile91Leu, NP_001365274.1:p.Ile91Val, NP_001365273.1:p.Ile89Leu, NP_001365273.1:p.Ile89Val, NP_001365276.1:p.Ile77Leu, NP_001365276.1:p.Ile77Val, XP_011521592.1:p.Ile121Leu, XP_011521592.1:p.Ile121Val, XP_011521593.1:p.Ile109Leu, XP_011521593.1:p.Ile109Val, XP_006721316.1:p.Ile134Leu, XP_006721316.1:p.Ile134Val, XP_006721319.1:p.Ile121Leu, XP_006721319.1:p.Ile121Val, XP_016879071.1:p.Ile109Leu, XP_016879071.1:p.Ile109Val, XP_011521595.1:p.Ile91Leu, XP_011521595.1:p.Ile91Val, XP_016879072.1:p.Ile121Leu, XP_016879072.1:p.Ile121Val, XP_047290465.1:p.Ile121Leu, XP_047290465.1:p.Ile121Val

                                        20.

                                        rs1436817167 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          T>C,G [Show Flanks]
                                          Chromosome:
                                          16:58511560 (GRCh38)
                                          16:58545464 (GRCh37)
                                          Canonical SPDI:
                                          NC_000016.10:58511559:T:C,NC_000016.10:58511559:T:G
                                          Gene:
                                          NDRG4 (Varview)
                                          Functional Consequence:
                                          intron_variant,coding_sequence_variant,missense_variant,non_coding_transcript_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          G=0./0 (ALFA)
                                          C=0.000004/1 (GnomAD_exomes)
                                          G=0.000008/2 (TOPMED)
                                          HGVS:
                                          NC_000016.10:g.58511560T>C, NC_000016.10:g.58511560T>G, NC_000016.9:g.58545464T>C, NC_000016.9:g.58545464T>G, NG_041803.1:g.52916T>C, NG_041803.1:g.52916T>G, NM_022910.4:c.1100T>C, NM_022910.4:c.1100T>G, NM_022910.3:c.1100T>C, NM_022910.3:c.1100T>G, NM_020465.4:c.1100T>C, NM_020465.4:c.1100T>G, NM_020465.3:c.1100T>C, NM_020465.3:c.1100T>G, NM_001363869.2:c.839T>C, NM_001363869.2:c.839T>G, NM_001363869.1:c.839T>C, NM_001363869.1:c.839T>G, NM_001130487.2:c.1160T>C, NM_001130487.2:c.1160T>G, NM_001130487.1:c.1160T>C, NM_001130487.1:c.1160T>G, NR_040072.2:n.1202T>C, NR_040072.2:n.1202T>G, NR_040072.1:n.1202T>C, NR_040072.1:n.1202T>G, NM_001242833.2:c.1094T>C, NM_001242833.2:c.1094T>G, NM_001242833.1:c.1094T>C, NM_001242833.1:c.1094T>G, NM_001242834.2:c.1058T>C, NM_001242834.2:c.1058T>G, NM_001242834.1:c.1058T>C, NM_001242834.1:c.1058T>G, NM_001242835.2:c.1043T>C, NM_001242835.2:c.1043T>G, NM_001242835.1:c.1043T>C, NM_001242835.1:c.1043T>G, NM_001242836.2:c.1004T>C, NM_001242836.2:c.1004T>G, NM_001242836.1:c.1004T>C, NM_001242836.1:c.1004T>G, NM_001378340.1:c.1190T>C, NM_001378340.1:c.1190T>G, NM_001378332.1:c.1289T>C, NM_001378332.1:c.1289T>G, NM_001378333.1:c.1253T>C, NM_001378333.1:c.1253T>G, NM_001378334.1:c.1250T>C, NM_001378334.1:c.1250T>G, NM_001378335.1:c.1214T>C, NM_001378335.1:c.1214T>G, NM_001378336.1:c.1199T>C, NM_001378336.1:c.1199T>G, NM_001378337.1:c.1193T>C, NM_001378337.1:c.1193T>G, NM_001378338.1:c.1193T>C, NM_001378338.1:c.1193T>G, NM_001378339.1:c.1190T>C, NM_001378339.1:c.1190T>G, NM_001378341.1:c.1178T>C, NM_001378341.1:c.1178T>G, NM_001378342.1:c.1154T>C, NM_001378342.1:c.1154T>G, NM_001378346.1:c.1100T>C, NM_001378346.1:c.1100T>G, NM_001378343.1:c.1139T>C, NM_001378343.1:c.1139T>G, NM_001378345.1:c.1139T>C, NM_001378345.1:c.1139T>G, NM_001378344.1:c.1133T>C, NM_001378344.1:c.1133T>G, NM_001378347.1:c.1097T>C, NM_001378347.1:c.1097T>G, XM_011523290.4:c.1229T>C, XM_011523290.4:c.1229T>G, XM_011523290.3:c.1229T>C, XM_011523290.3:c.1229T>G, XM_011523290.2:c.1229T>C, XM_011523290.2:c.1229T>G, XM_011523290.1:c.1229T>C, XM_011523290.1:c.1229T>G, XM_011523291.4:c.1193T>C, XM_011523291.4:c.1193T>G, XM_011523291.3:c.1193T>C, XM_011523291.3:c.1193T>G, XM_011523291.2:c.1193T>C, XM_011523291.2:c.1193T>G, XM_011523291.1:c.1193T>C, XM_011523291.1:c.1193T>G, XM_006721253.4:c.1268T>C, XM_006721253.4:c.1268T>G, XM_006721253.3:c.1268T>C, XM_006721253.3:c.1268T>G, XM_006721253.2:c.1268T>C, XM_006721253.2:c.1268T>G, XM_006721253.1:c.1268T>C, XM_006721253.1:c.1268T>G, XM_006721256.4:c.1229T>C, XM_006721256.4:c.1229T>G, XM_006721256.3:c.1229T>C, XM_006721256.3:c.1229T>G, XM_006721256.2:c.1229T>C, XM_006721256.2:c.1229T>G, XM_006721256.1:c.1229T>C, XM_006721256.1:c.1229T>G, XM_017023582.3:c.1154T>C, XM_017023582.3:c.1154T>G, XM_017023582.2:c.1154T>C, XM_017023582.2:c.1154T>G, XM_017023582.1:c.1154T>C, XM_017023582.1:c.1154T>G, XM_011523293.3:c.1139T>C, XM_011523293.3:c.1139T>G, XM_011523293.2:c.1139T>C, XM_011523293.2:c.1139T>G, XM_011523293.1:c.1139T>C, XM_011523293.1:c.1139T>G, XM_047434509.1:c.1229T>C, XM_047434509.1:c.1229T>G, NP_075061.1:p.Met367Thr, NP_075061.1:p.Met367Arg, NP_065198.1:p.Met367Thr, NP_065198.1:p.Met367Arg, NP_001350798.1:p.Met280Thr, NP_001350798.1:p.Met280Arg, NP_001123959.1:p.Met387Thr, NP_001123959.1:p.Met387Arg, NP_001229762.1:p.Met365Thr, NP_001229762.1:p.Met365Arg, NP_001229763.1:p.Met353Thr, NP_001229763.1:p.Met353Arg, NP_001229764.1:p.Met348Thr, NP_001229764.1:p.Met348Arg, NP_001229765.1:p.Met335Thr, NP_001229765.1:p.Met335Arg, NP_001365269.1:p.Met397Thr, NP_001365269.1:p.Met397Arg, NP_001365261.1:p.Met430Thr, NP_001365261.1:p.Met430Arg, NP_001365262.1:p.Met418Thr, NP_001365262.1:p.Met418Arg, NP_001365263.1:p.Met417Thr, NP_001365263.1:p.Met417Arg, NP_001365264.1:p.Met405Thr, NP_001365264.1:p.Met405Arg, NP_001365265.1:p.Met400Thr, NP_001365265.1:p.Met400Arg, NP_001365266.1:p.Met398Thr, NP_001365266.1:p.Met398Arg, NP_001365267.1:p.Met398Thr, NP_001365267.1:p.Met398Arg, NP_001365268.1:p.Met397Thr, NP_001365268.1:p.Met397Arg, NP_001365270.1:p.Met393Thr, NP_001365270.1:p.Met393Arg, NP_001365271.1:p.Met385Thr, NP_001365271.1:p.Met385Arg, NP_001365275.1:p.Met367Thr, NP_001365275.1:p.Met367Arg, NP_001365272.1:p.Met380Thr, NP_001365272.1:p.Met380Arg, NP_001365274.1:p.Met380Thr, NP_001365274.1:p.Met380Arg, NP_001365273.1:p.Met378Thr, NP_001365273.1:p.Met378Arg, NP_001365276.1:p.Met366Thr, NP_001365276.1:p.Met366Arg, XP_011521592.1:p.Met410Thr, XP_011521592.1:p.Met410Arg, XP_011521593.1:p.Met398Thr, XP_011521593.1:p.Met398Arg, XP_006721316.1:p.Met423Thr, XP_006721316.1:p.Met423Arg, XP_006721319.1:p.Met410Thr, XP_006721319.1:p.Met410Arg, XP_016879071.1:p.Met385Thr, XP_016879071.1:p.Met385Arg, XP_011521595.1:p.Met380Thr, XP_011521595.1:p.Met380Arg, XP_047290465.1:p.Met410Thr, XP_047290465.1:p.Met410Arg

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