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Links from Protein

Items: 1 to 20 of 346

1.

rs1481745191 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>A,C [Show Flanks]
    Chromosome:
    14:21017744 (GRCh38)
    14:21485903 (GRCh37)
    Canonical SPDI:
    NC_000014.9:21017743:G:A,NC_000014.9:21017743:G:C
    Gene:
    NDRG2 (Varview)
    Functional Consequence:
    coding_sequence_variant,missense_variant,3_prime_UTR_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    C=0./0 (ALFA)
    A=0.000004/1 (TOPMED)
    A=0.000007/1 (GnomAD)
    HGVS:
    NC_000014.9:g.21017744G>A, NC_000014.9:g.21017744G>C, NC_000014.8:g.21485903G>A, NC_000014.8:g.21485903G>C, NM_016250.3:c.926C>T, NM_016250.3:c.926C>G, NM_016250.2:c.926C>T, NM_016250.2:c.926C>G, NM_001320329.2:c.968C>T, NM_001320329.2:c.968C>G, NM_001320329.1:c.968C>T, NM_001320329.1:c.968C>G, NM_001354565.2:c.968C>T, NM_001354565.2:c.968C>G, NM_001354565.1:c.968C>T, NM_001354565.1:c.968C>G, NM_001354568.2:c.926C>T, NM_001354568.2:c.926C>G, NM_001354568.1:c.926C>T, NM_001354568.1:c.926C>G, NM_001354570.2:c.968C>T, NM_001354570.2:c.968C>G, NM_001354570.1:c.968C>T, NM_001354570.1:c.968C>G, NM_001354567.2:c.968C>T, NM_001354567.2:c.968C>G, NM_001354567.1:c.968C>T, NM_001354567.1:c.968C>G, NM_001282212.2:c.878C>T, NM_001282212.2:c.878C>G, NM_001282212.1:c.878C>T, NM_001282212.1:c.878C>G, NM_001282214.2:c.926C>T, NM_001282214.2:c.926C>G, NM_001282214.1:c.926C>T, NM_001282214.1:c.926C>G, NM_001354561.2:c.926C>T, NM_001354561.2:c.926C>G, NM_001354561.1:c.926C>T, NM_001354561.1:c.926C>G, NM_001282213.2:c.926C>T, NM_001282213.2:c.926C>G, NM_001282213.1:c.926C>T, NM_001282213.1:c.926C>G, NM_001354559.2:c.968C>T, NM_001354559.2:c.968C>G, NM_001354559.1:c.968C>T, NM_001354559.1:c.968C>G, NM_201535.2:c.968C>T, NM_201535.2:c.968C>G, NM_201535.1:c.968C>T, NM_201535.1:c.968C>G, NM_001354562.2:c.968C>T, NM_001354562.2:c.968C>G, NM_001354562.1:c.968C>T, NM_001354562.1:c.968C>G, NM_201540.2:c.968C>T, NM_201540.2:c.968C>G, NM_201540.1:c.968C>T, NM_201540.1:c.968C>G, NM_001354558.2:c.1022C>T, NM_001354558.2:c.1022C>G, NM_001354558.1:c.1022C>T, NM_001354558.1:c.1022C>G, NM_201537.2:c.968C>T, NM_201537.2:c.968C>G, NM_201537.1:c.968C>T, NM_201537.1:c.968C>G, NM_201541.2:c.926C>T, NM_201541.2:c.926C>G, NM_201541.1:c.926C>T, NM_201541.1:c.926C>G, NM_001282215.2:c.935C>T, NM_001282215.2:c.935C>G, NM_001282215.1:c.935C>T, NM_001282215.1:c.935C>G, NM_201536.2:c.926C>T, NM_201536.2:c.926C>G, NM_201536.1:c.926C>T, NM_201536.1:c.926C>G, NM_201539.2:c.968C>T, NM_201539.2:c.968C>G, NM_201539.1:c.968C>T, NM_201539.1:c.968C>G, NM_001354564.2:c.*58C>T, NM_001354564.2:c.*58C>G, NM_001354564.1:c.*58C>T, NM_001354564.1:c.*58C>G, NM_001282211.2:c.956C>T, NM_001282211.2:c.956C>G, NM_001282211.1:c.956C>T, NM_001282211.1:c.956C>G, NM_201538.2:c.926C>T, NM_201538.2:c.926C>G, NM_201538.1:c.926C>T, NM_201538.1:c.926C>G, NM_001282216.2:c.788C>T, NM_001282216.2:c.788C>G, NM_001282216.1:c.788C>T, NM_001282216.1:c.788C>G, NM_001354560.2:c.893C>T, NM_001354560.2:c.893C>G, NM_001354560.1:c.893C>T, NM_001354560.1:c.893C>G, NM_001354569.1:c.926C>T, NM_001354569.1:c.926C>G, NM_001354566.1:c.968C>T, NM_001354566.1:c.968C>G, NP_057334.1:p.Thr309Ile, NP_057334.1:p.Thr309Ser, NP_001307258.1:p.Thr323Ile, NP_001307258.1:p.Thr323Ser, NP_001341494.1:p.Thr323Ile, NP_001341494.1:p.Thr323Ser, NP_001341497.1:p.Thr309Ile, NP_001341497.1:p.Thr309Ser, NP_001341499.1:p.Thr323Ile, NP_001341499.1:p.Thr323Ser, NP_001341496.1:p.Thr323Ile, NP_001341496.1:p.Thr323Ser, NP_001269141.1:p.Thr293Ile, NP_001269141.1:p.Thr293Ser, NP_001269143.1:p.Thr309Ile, NP_001269143.1:p.Thr309Ser, NP_001341490.1:p.Thr309Ile, NP_001341490.1:p.Thr309Ser, NP_001269142.1:p.Thr309Ile, NP_001269142.1:p.Thr309Ser, NP_001341488.1:p.Thr323Ile, NP_001341488.1:p.Thr323Ser, NP_963293.1:p.Thr323Ile, NP_963293.1:p.Thr323Ser, NP_001341491.1:p.Thr323Ile, NP_001341491.1:p.Thr323Ser, NP_963834.1:p.Thr323Ile, NP_963834.1:p.Thr323Ser, NP_001341487.1:p.Thr341Ile, NP_001341487.1:p.Thr341Ser, NP_963831.1:p.Thr323Ile, NP_963831.1:p.Thr323Ser, NP_963835.1:p.Thr309Ile, NP_963835.1:p.Thr309Ser, NP_001269144.1:p.Thr312Ile, NP_001269144.1:p.Thr312Ser, NP_963294.1:p.Thr309Ile, NP_963294.1:p.Thr309Ser, NP_963833.1:p.Thr323Ile, NP_963833.1:p.Thr323Ser, NP_001269140.1:p.Thr319Ile, NP_001269140.1:p.Thr319Ser, NP_963832.1:p.Thr309Ile, NP_963832.1:p.Thr309Ser, NP_001269145.1:p.Thr263Ile, NP_001269145.1:p.Thr263Ser, NP_001341489.1:p.Thr298Ile, NP_001341489.1:p.Thr298Ser, NP_001341498.1:p.Thr309Ile, NP_001341498.1:p.Thr309Ser, NP_001341495.1:p.Thr323Ile, NP_001341495.1:p.Thr323Ser

    2.

    rs1468162416 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      C>A,G [Show Flanks]
      Chromosome:
      14:21022062 (GRCh38)
      14:21490221 (GRCh37)
      Canonical SPDI:
      NC_000014.9:21022061:C:A,NC_000014.9:21022061:C:G
      Gene:
      NDRG2 (Varview)
      Functional Consequence:
      missense_variant,coding_sequence_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      G=0./0 (ALFA)
      G=0.000008/2 (TOPMED)
      G=0.000014/2 (GnomAD)
      HGVS:
      NC_000014.9:g.21022062C>A, NC_000014.9:g.21022062C>G, NC_000014.8:g.21490221C>A, NC_000014.8:g.21490221C>G, NM_016250.3:c.302G>T, NM_016250.3:c.302G>C, NM_016250.2:c.302G>T, NM_016250.2:c.302G>C, NM_001320329.2:c.344G>T, NM_001320329.2:c.344G>C, NM_001320329.1:c.344G>T, NM_001320329.1:c.344G>C, NM_001354565.2:c.344G>T, NM_001354565.2:c.344G>C, NM_001354565.1:c.344G>T, NM_001354565.1:c.344G>C, NM_001354568.2:c.302G>T, NM_001354568.2:c.302G>C, NM_001354568.1:c.302G>T, NM_001354568.1:c.302G>C, NM_001354570.2:c.344G>T, NM_001354570.2:c.344G>C, NM_001354570.1:c.344G>T, NM_001354570.1:c.344G>C, NM_001354567.2:c.344G>T, NM_001354567.2:c.344G>C, NM_001354567.1:c.344G>T, NM_001354567.1:c.344G>C, NM_001282212.2:c.302G>T, NM_001282212.2:c.302G>C, NM_001282212.1:c.302G>T, NM_001282212.1:c.302G>C, NM_001282214.2:c.302G>T, NM_001282214.2:c.302G>C, NM_001282214.1:c.302G>T, NM_001282214.1:c.302G>C, NM_001354561.2:c.302G>T, NM_001354561.2:c.302G>C, NM_001354561.1:c.302G>T, NM_001354561.1:c.302G>C, NM_001282213.2:c.302G>T, NM_001282213.2:c.302G>C, NM_001282213.1:c.302G>T, NM_001282213.1:c.302G>C, NM_001354559.2:c.344G>T, NM_001354559.2:c.344G>C, NM_001354559.1:c.344G>T, NM_001354559.1:c.344G>C, NM_201535.2:c.344G>T, NM_201535.2:c.344G>C, NM_201535.1:c.344G>T, NM_201535.1:c.344G>C, NM_001354562.2:c.344G>T, NM_001354562.2:c.344G>C, NM_001354562.1:c.344G>T, NM_001354562.1:c.344G>C, NM_201540.2:c.344G>T, NM_201540.2:c.344G>C, NM_201540.1:c.344G>T, NM_201540.1:c.344G>C, NM_001354558.2:c.344G>T, NM_001354558.2:c.344G>C, NM_001354558.1:c.344G>T, NM_001354558.1:c.344G>C, NM_201537.2:c.344G>T, NM_201537.2:c.344G>C, NM_201537.1:c.344G>T, NM_201537.1:c.344G>C, NM_201541.2:c.302G>T, NM_201541.2:c.302G>C, NM_201541.1:c.302G>T, NM_201541.1:c.302G>C, NM_001282215.2:c.344G>T, NM_001282215.2:c.344G>C, NM_001282215.1:c.344G>T, NM_001282215.1:c.344G>C, NM_201536.2:c.302G>T, NM_201536.2:c.302G>C, NM_201536.1:c.302G>T, NM_201536.1:c.302G>C, NM_201539.2:c.344G>T, NM_201539.2:c.344G>C, NM_201539.1:c.344G>T, NM_201539.1:c.344G>C, NM_001354564.2:c.344G>T, NM_001354564.2:c.344G>C, NM_001354564.1:c.344G>T, NM_001354564.1:c.344G>C, NM_001282211.2:c.332G>T, NM_001282211.2:c.332G>C, NM_001282211.1:c.332G>T, NM_001282211.1:c.332G>C, NM_201538.2:c.302G>T, NM_201538.2:c.302G>C, NM_201538.1:c.302G>T, NM_201538.1:c.302G>C, NM_001282216.2:c.164G>T, NM_001282216.2:c.164G>C, NM_001282216.1:c.164G>T, NM_001282216.1:c.164G>C, NM_001354560.2:c.302G>T, NM_001354560.2:c.302G>C, NM_001354560.1:c.302G>T, NM_001354560.1:c.302G>C, NM_001354569.1:c.302G>T, NM_001354569.1:c.302G>C, NM_001354566.1:c.344G>T, NM_001354566.1:c.344G>C, NP_057334.1:p.Gly101Val, NP_057334.1:p.Gly101Ala, NP_001307258.1:p.Gly115Val, NP_001307258.1:p.Gly115Ala, NP_001341494.1:p.Gly115Val, NP_001341494.1:p.Gly115Ala, NP_001341497.1:p.Gly101Val, NP_001341497.1:p.Gly101Ala, NP_001341499.1:p.Gly115Val, NP_001341499.1:p.Gly115Ala, NP_001341496.1:p.Gly115Val, NP_001341496.1:p.Gly115Ala, NP_001269141.1:p.Gly101Val, NP_001269141.1:p.Gly101Ala, NP_001269143.1:p.Gly101Val, NP_001269143.1:p.Gly101Ala, NP_001341490.1:p.Gly101Val, NP_001341490.1:p.Gly101Ala, NP_001269142.1:p.Gly101Val, NP_001269142.1:p.Gly101Ala, NP_001341488.1:p.Gly115Val, NP_001341488.1:p.Gly115Ala, NP_963293.1:p.Gly115Val, NP_963293.1:p.Gly115Ala, NP_001341491.1:p.Gly115Val, NP_001341491.1:p.Gly115Ala, NP_963834.1:p.Gly115Val, NP_963834.1:p.Gly115Ala, NP_001341487.1:p.Gly115Val, NP_001341487.1:p.Gly115Ala, NP_963831.1:p.Gly115Val, NP_963831.1:p.Gly115Ala, NP_963835.1:p.Gly101Val, NP_963835.1:p.Gly101Ala, NP_001269144.1:p.Gly115Val, NP_001269144.1:p.Gly115Ala, NP_963294.1:p.Gly101Val, NP_963294.1:p.Gly101Ala, NP_963833.1:p.Gly115Val, NP_963833.1:p.Gly115Ala, NP_001341493.1:p.Gly115Val, NP_001341493.1:p.Gly115Ala, NP_001269140.1:p.Gly111Val, NP_001269140.1:p.Gly111Ala, NP_963832.1:p.Gly101Val, NP_963832.1:p.Gly101Ala, NP_001269145.1:p.Gly55Val, NP_001269145.1:p.Gly55Ala, NP_001341489.1:p.Gly101Val, NP_001341489.1:p.Gly101Ala, NP_001341498.1:p.Gly101Val, NP_001341498.1:p.Gly101Ala, NP_001341495.1:p.Gly115Val, NP_001341495.1:p.Gly115Ala

      3.

      rs1466516055 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        T>C,G [Show Flanks]
        Chromosome:
        14:21019700 (GRCh38)
        14:21487859 (GRCh37)
        Canonical SPDI:
        NC_000014.9:21019699:T:C,NC_000014.9:21019699:T:G
        Gene:
        NDRG2 (Varview)
        Functional Consequence:
        missense_variant,coding_sequence_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        G=0.000028/1 (ALFA)
        G=0.000011/3 (TOPMED)
        G=0.000021/3 (GnomAD)
        HGVS:
        NC_000014.9:g.21019700T>C, NC_000014.9:g.21019700T>G, NC_000014.8:g.21487859T>C, NC_000014.8:g.21487859T>G, NM_016250.3:c.613A>G, NM_016250.3:c.613A>C, NM_016250.2:c.613A>G, NM_016250.2:c.613A>C, NM_001320329.2:c.655A>G, NM_001320329.2:c.655A>C, NM_001320329.1:c.655A>G, NM_001320329.1:c.655A>C, NM_001354565.2:c.655A>G, NM_001354565.2:c.655A>C, NM_001354565.1:c.655A>G, NM_001354565.1:c.655A>C, NM_001354568.2:c.613A>G, NM_001354568.2:c.613A>C, NM_001354568.1:c.613A>G, NM_001354568.1:c.613A>C, NM_001354570.2:c.655A>G, NM_001354570.2:c.655A>C, NM_001354570.1:c.655A>G, NM_001354570.1:c.655A>C, NM_001354567.2:c.655A>G, NM_001354567.2:c.655A>C, NM_001354567.1:c.655A>G, NM_001354567.1:c.655A>C, NM_001282212.2:c.613A>G, NM_001282212.2:c.613A>C, NM_001282212.1:c.613A>G, NM_001282212.1:c.613A>C, NM_001282214.2:c.613A>G, NM_001282214.2:c.613A>C, NM_001282214.1:c.613A>G, NM_001282214.1:c.613A>C, NM_001354561.2:c.613A>G, NM_001354561.2:c.613A>C, NM_001354561.1:c.613A>G, NM_001354561.1:c.613A>C, NM_001282213.2:c.613A>G, NM_001282213.2:c.613A>C, NM_001282213.1:c.613A>G, NM_001282213.1:c.613A>C, NM_001354559.2:c.655A>G, NM_001354559.2:c.655A>C, NM_001354559.1:c.655A>G, NM_001354559.1:c.655A>C, NM_201535.2:c.655A>G, NM_201535.2:c.655A>C, NM_201535.1:c.655A>G, NM_201535.1:c.655A>C, NM_001354562.2:c.655A>G, NM_001354562.2:c.655A>C, NM_001354562.1:c.655A>G, NM_001354562.1:c.655A>C, NM_201540.2:c.655A>G, NM_201540.2:c.655A>C, NM_201540.1:c.655A>G, NM_201540.1:c.655A>C, NM_001354558.2:c.655A>G, NM_001354558.2:c.655A>C, NM_001354558.1:c.655A>G, NM_001354558.1:c.655A>C, NM_201537.2:c.655A>G, NM_201537.2:c.655A>C, NM_201537.1:c.655A>G, NM_201537.1:c.655A>C, NM_201541.2:c.613A>G, NM_201541.2:c.613A>C, NM_201541.1:c.613A>G, NM_201541.1:c.613A>C, NM_001282215.2:c.655A>G, NM_001282215.2:c.655A>C, NM_001282215.1:c.655A>G, NM_001282215.1:c.655A>C, NM_201536.2:c.613A>G, NM_201536.2:c.613A>C, NM_201536.1:c.613A>G, NM_201536.1:c.613A>C, NM_201539.2:c.655A>G, NM_201539.2:c.655A>C, NM_201539.1:c.655A>G, NM_201539.1:c.655A>C, NM_001354564.2:c.655A>G, NM_001354564.2:c.655A>C, NM_001354564.1:c.655A>G, NM_001354564.1:c.655A>C, NM_001282211.2:c.643A>G, NM_001282211.2:c.643A>C, NM_001282211.1:c.643A>G, NM_001282211.1:c.643A>C, NM_201538.2:c.613A>G, NM_201538.2:c.613A>C, NM_201538.1:c.613A>G, NM_201538.1:c.613A>C, NM_001282216.2:c.475A>G, NM_001282216.2:c.475A>C, NM_001282216.1:c.475A>G, NM_001282216.1:c.475A>C, NM_001354560.2:c.613A>G, NM_001354560.2:c.613A>C, NM_001354560.1:c.613A>G, NM_001354560.1:c.613A>C, NM_001354569.1:c.613A>G, NM_001354569.1:c.613A>C, NM_001354566.1:c.655A>G, NM_001354566.1:c.655A>C, NP_057334.1:p.Asn205Asp, NP_057334.1:p.Asn205His, NP_001307258.1:p.Asn219Asp, NP_001307258.1:p.Asn219His, NP_001341494.1:p.Asn219Asp, NP_001341494.1:p.Asn219His, NP_001341497.1:p.Asn205Asp, NP_001341497.1:p.Asn205His, NP_001341499.1:p.Asn219Asp, NP_001341499.1:p.Asn219His, NP_001341496.1:p.Asn219Asp, NP_001341496.1:p.Asn219His, NP_001269141.1:p.Asn205Asp, NP_001269141.1:p.Asn205His, NP_001269143.1:p.Asn205Asp, NP_001269143.1:p.Asn205His, NP_001341490.1:p.Asn205Asp, NP_001341490.1:p.Asn205His, NP_001269142.1:p.Asn205Asp, NP_001269142.1:p.Asn205His, NP_001341488.1:p.Asn219Asp, NP_001341488.1:p.Asn219His, NP_963293.1:p.Asn219Asp, NP_963293.1:p.Asn219His, NP_001341491.1:p.Asn219Asp, NP_001341491.1:p.Asn219His, NP_963834.1:p.Asn219Asp, NP_963834.1:p.Asn219His, NP_001341487.1:p.Asn219Asp, NP_001341487.1:p.Asn219His, NP_963831.1:p.Asn219Asp, NP_963831.1:p.Asn219His, NP_963835.1:p.Asn205Asp, NP_963835.1:p.Asn205His, NP_001269144.1:p.Asn219Asp, NP_001269144.1:p.Asn219His, NP_963294.1:p.Asn205Asp, NP_963294.1:p.Asn205His, NP_963833.1:p.Asn219Asp, NP_963833.1:p.Asn219His, NP_001341493.1:p.Asn219Asp, NP_001341493.1:p.Asn219His, NP_001269140.1:p.Asn215Asp, NP_001269140.1:p.Asn215His, NP_963832.1:p.Asn205Asp, NP_963832.1:p.Asn205His, NP_001269145.1:p.Asn159Asp, NP_001269145.1:p.Asn159His, NP_001341489.1:p.Asn205Asp, NP_001341489.1:p.Asn205His, NP_001341498.1:p.Asn205Asp, NP_001341498.1:p.Asn205His, NP_001341495.1:p.Asn219Asp, NP_001341495.1:p.Asn219His

        4.

        rs1461778475 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          C>G [Show Flanks]
          Chromosome:
          14:21017721 (GRCh38)
          14:21485880 (GRCh37)
          Canonical SPDI:
          NC_000014.9:21017720:C:G
          Gene:
          NDRG2 (Varview)
          Functional Consequence:
          missense_variant,coding_sequence_variant,3_prime_UTR_variant
          Validated:
          by frequency
          MAF:
          G=0.000004/1 (GnomAD_exomes)
          HGVS:
          NC_000014.9:g.21017721C>G, NC_000014.8:g.21485880C>G, NM_016250.3:c.949G>C, NM_016250.2:c.949G>C, NM_001320329.2:c.991G>C, NM_001320329.1:c.991G>C, NM_001354565.2:c.991G>C, NM_001354565.1:c.991G>C, NM_001354568.2:c.949G>C, NM_001354568.1:c.949G>C, NM_001354570.2:c.991G>C, NM_001354570.1:c.991G>C, NM_001354567.2:c.991G>C, NM_001354567.1:c.991G>C, NM_001282212.2:c.901G>C, NM_001282212.1:c.901G>C, NM_001282214.2:c.949G>C, NM_001282214.1:c.949G>C, NM_001354561.2:c.949G>C, NM_001354561.1:c.949G>C, NM_001282213.2:c.949G>C, NM_001282213.1:c.949G>C, NM_001354559.2:c.991G>C, NM_001354559.1:c.991G>C, NM_201535.2:c.991G>C, NM_201535.1:c.991G>C, NM_001354562.2:c.991G>C, NM_001354562.1:c.991G>C, NM_201540.2:c.991G>C, NM_201540.1:c.991G>C, NM_001354558.2:c.1045G>C, NM_001354558.1:c.1045G>C, NM_201537.2:c.991G>C, NM_201537.1:c.991G>C, NM_201541.2:c.949G>C, NM_201541.1:c.949G>C, NM_001282215.2:c.958G>C, NM_001282215.1:c.958G>C, NM_201536.2:c.949G>C, NM_201536.1:c.949G>C, NM_201539.2:c.991G>C, NM_201539.1:c.991G>C, NM_001354564.2:c.*81G>C, NM_001354564.1:c.*81G>C, NM_001282211.2:c.979G>C, NM_001282211.1:c.979G>C, NM_201538.2:c.949G>C, NM_201538.1:c.949G>C, NM_001282216.2:c.811G>C, NM_001282216.1:c.811G>C, NM_001354560.2:c.916G>C, NM_001354560.1:c.916G>C, NM_001354569.1:c.949G>C, NM_001354566.1:c.991G>C, NP_057334.1:p.Ala317Pro, NP_001307258.1:p.Ala331Pro, NP_001341494.1:p.Ala331Pro, NP_001341497.1:p.Ala317Pro, NP_001341499.1:p.Ala331Pro, NP_001341496.1:p.Ala331Pro, NP_001269141.1:p.Ala301Pro, NP_001269143.1:p.Ala317Pro, NP_001341490.1:p.Ala317Pro, NP_001269142.1:p.Ala317Pro, NP_001341488.1:p.Ala331Pro, NP_963293.1:p.Ala331Pro, NP_001341491.1:p.Ala331Pro, NP_963834.1:p.Ala331Pro, NP_001341487.1:p.Ala349Pro, NP_963831.1:p.Ala331Pro, NP_963835.1:p.Ala317Pro, NP_001269144.1:p.Ala320Pro, NP_963294.1:p.Ala317Pro, NP_963833.1:p.Ala331Pro, NP_001269140.1:p.Ala327Pro, NP_963832.1:p.Ala317Pro, NP_001269145.1:p.Ala271Pro, NP_001341489.1:p.Ala306Pro, NP_001341498.1:p.Ala317Pro, NP_001341495.1:p.Ala331Pro

          5.

          rs1458370071 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            A>G [Show Flanks]
            Chromosome:
            14:21020829 (GRCh38)
            14:21488988 (GRCh37)
            Canonical SPDI:
            NC_000014.9:21020828:A:G
            Gene:
            NDRG2 (Varview)
            Functional Consequence:
            synonymous_variant,coding_sequence_variant
            Validated:
            by frequency
            MAF:
            G=0.000004/1 (GnomAD_exomes)
            HGVS:
            NC_000014.9:g.21020829A>G, NC_000014.8:g.21488988A>G, NM_016250.3:c.381T>C, NM_016250.2:c.381T>C, NM_001320329.2:c.423T>C, NM_001320329.1:c.423T>C, NM_001354565.2:c.423T>C, NM_001354565.1:c.423T>C, NM_001354568.2:c.381T>C, NM_001354568.1:c.381T>C, NM_001354570.2:c.423T>C, NM_001354570.1:c.423T>C, NM_001354567.2:c.423T>C, NM_001354567.1:c.423T>C, NM_001282212.2:c.381T>C, NM_001282212.1:c.381T>C, NM_001282214.2:c.381T>C, NM_001282214.1:c.381T>C, NM_001354561.2:c.381T>C, NM_001354561.1:c.381T>C, NM_001282213.2:c.381T>C, NM_001282213.1:c.381T>C, NM_001354559.2:c.423T>C, NM_001354559.1:c.423T>C, NM_201535.2:c.423T>C, NM_201535.1:c.423T>C, NM_001354562.2:c.423T>C, NM_001354562.1:c.423T>C, NM_201540.2:c.423T>C, NM_201540.1:c.423T>C, NM_001354558.2:c.423T>C, NM_001354558.1:c.423T>C, NM_201537.2:c.423T>C, NM_201537.1:c.423T>C, NM_201541.2:c.381T>C, NM_201541.1:c.381T>C, NM_001282215.2:c.423T>C, NM_001282215.1:c.423T>C, NM_201536.2:c.381T>C, NM_201536.1:c.381T>C, NM_201539.2:c.423T>C, NM_201539.1:c.423T>C, NM_001354564.2:c.423T>C, NM_001354564.1:c.423T>C, NM_001282211.2:c.411T>C, NM_001282211.1:c.411T>C, NM_201538.2:c.381T>C, NM_201538.1:c.381T>C, NM_001282216.2:c.243T>C, NM_001282216.1:c.243T>C, NM_001354560.2:c.381T>C, NM_001354560.1:c.381T>C, NM_001354569.1:c.381T>C, NM_001354566.1:c.423T>C

            6.

            rs1457374701 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              G>T [Show Flanks]
              Chromosome:
              14:21019124 (GRCh38)
              14:21487283 (GRCh37)
              Canonical SPDI:
              NC_000014.9:21019123:G:T
              Gene:
              NDRG2 (Varview)
              Functional Consequence:
              synonymous_variant,coding_sequence_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              T=0./0 (ALFA)
              T=0./0 (GnomAD)
              T=0.000012/3 (GnomAD_exomes)
              HGVS:
              NC_000014.9:g.21019124G>T, NC_000014.8:g.21487283G>T, NM_016250.3:c.711C>A, NM_016250.2:c.711C>A, NM_001320329.2:c.753C>A, NM_001320329.1:c.753C>A, NM_001354565.2:c.753C>A, NM_001354565.1:c.753C>A, NM_001354568.2:c.711C>A, NM_001354568.1:c.711C>A, NM_001354570.2:c.753C>A, NM_001354570.1:c.753C>A, NM_001354567.2:c.753C>A, NM_001354567.1:c.753C>A, NM_001282212.2:c.711C>A, NM_001282212.1:c.711C>A, NM_001282214.2:c.711C>A, NM_001282214.1:c.711C>A, NM_001354561.2:c.711C>A, NM_001354561.1:c.711C>A, NM_001282213.2:c.711C>A, NM_001282213.1:c.711C>A, NM_001354559.2:c.753C>A, NM_001354559.1:c.753C>A, NM_201535.2:c.753C>A, NM_201535.1:c.753C>A, NM_001354562.2:c.753C>A, NM_001354562.1:c.753C>A, NM_201540.2:c.753C>A, NM_201540.1:c.753C>A, NM_001354558.2:c.753C>A, NM_001354558.1:c.753C>A, NM_201537.2:c.753C>A, NM_201537.1:c.753C>A, NM_201541.2:c.711C>A, NM_201541.1:c.711C>A, NM_001282215.2:c.753C>A, NM_001282215.1:c.753C>A, NM_201536.2:c.711C>A, NM_201536.1:c.711C>A, NM_201539.2:c.753C>A, NM_201539.1:c.753C>A, NM_001354564.2:c.753C>A, NM_001354564.1:c.753C>A, NM_001282211.2:c.741C>A, NM_001282211.1:c.741C>A, NM_201538.2:c.711C>A, NM_201538.1:c.711C>A, NM_001282216.2:c.573C>A, NM_001282216.1:c.573C>A, NM_001354560.2:c.711C>A, NM_001354560.1:c.711C>A, NM_001354569.1:c.711C>A, NM_001354566.1:c.753C>A

              7.

              rs1456646256 [Homo sapiens]
                Variant type:
                DELINS
                Alleles:
                GCC>- [Show Flanks]
                Chromosome:
                14:21023248 (GRCh38)
                14:21491407 (GRCh37)
                Canonical SPDI:
                NC_000014.9:21023244:GCCGCC:GCC
                Gene:
                NDRG2 (Varview), TPPP2 (Varview), MIR6717 (Varview)
                Functional Consequence:
                500B_downstream_variant,coding_sequence_variant,upstream_transcript_variant,2KB_upstream_variant,downstream_transcript_variant,inframe_deletion,5_prime_UTR_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                GCCGCC=0./0 (ALFA)
                -=0.000004/1 (GnomAD_exomes)
                -=0.000008/2 (TOPMED)
                HGVS:
                NC_000014.9:g.21023245GCC[1], NC_000014.8:g.21491404GCC[1], NM_016250.3:c.66GGC[1], NM_016250.2:c.66GGC[1], NM_001320329.2:c.66GGC[1], NM_001320329.1:c.66GGC[1], NM_001354565.2:c.66GGC[1], NM_001354565.1:c.66GGC[1], NM_001354568.2:c.66GGC[1], NM_001354568.1:c.66GGC[1], NM_001354570.2:c.66GGC[1], NM_001354570.1:c.66GGC[1], NM_001354567.2:c.66GGC[1], NM_001354567.1:c.66GGC[1], NM_001282212.2:c.66GGC[1], NM_001282212.1:c.66GGC[1], NM_001282214.2:c.66GGC[1], NM_001282214.1:c.66GGC[1], NM_001354561.2:c.66GGC[1], NM_001354561.1:c.66GGC[1], NM_001282213.2:c.66GGC[1], NM_001282213.1:c.66GGC[1], NM_001354559.2:c.66GGC[1], NM_001354559.1:c.66GGC[1], NM_201535.2:c.66GGC[1], NM_201535.1:c.66GGC[1], NM_001354562.2:c.66GGC[1], NM_001354562.1:c.66GGC[1], NM_201540.2:c.66GGC[1], NM_201540.1:c.66GGC[1], NM_001354558.2:c.66GGC[1], NM_001354558.1:c.66GGC[1], NM_201537.2:c.66GGC[1], NM_201537.1:c.66GGC[1], NM_201541.2:c.66GGC[1], NM_201541.1:c.66GGC[1], NM_001282215.2:c.66GGC[1], NM_001282215.1:c.66GGC[1], NM_201536.2:c.66GGC[1], NM_201536.1:c.66GGC[1], NM_201539.2:c.66GGC[1], NM_201539.1:c.66GGC[1], NM_001354564.2:c.66GGC[1], NM_001354564.1:c.66GGC[1], NM_001282211.2:c.96GGC[1], NM_001282211.1:c.96GGC[1], NM_201538.2:c.66GGC[1], NM_201538.1:c.66GGC[1], NM_001282216.2:c.-56GGC[1], NM_001282216.1:c.-56GGC[1], NM_001354560.2:c.66GGC[1], NM_001354560.1:c.66GGC[1], NM_001354569.1:c.66GGC[1], NM_001354566.1:c.66GGC[1], NP_057334.1:p.Ala24del, NP_001307258.1:p.Ala24del, NP_001341494.1:p.Ala24del, NP_001341497.1:p.Ala24del, NP_001341499.1:p.Ala24del, NP_001341496.1:p.Ala24del, NP_001269141.1:p.Ala24del, NP_001269143.1:p.Ala24del, NP_001341490.1:p.Ala24del, NP_001269142.1:p.Ala24del, NP_001341488.1:p.Ala24del, NP_963293.1:p.Ala24del, NP_001341491.1:p.Ala24del, NP_963834.1:p.Ala24del, NP_001341487.1:p.Ala24del, NP_963831.1:p.Ala24del, NP_963835.1:p.Ala24del, NP_001269144.1:p.Ala24del, NP_963294.1:p.Ala24del, NP_963833.1:p.Ala24del, NP_001341493.1:p.Ala24del, NP_001269140.1:p.Ala34del, NP_963832.1:p.Ala24del, NP_001341489.1:p.Ala24del, NP_001341498.1:p.Ala24del, NP_001341495.1:p.Ala24del

                8.

                rs1455066473 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  G>A,T [Show Flanks]
                  Chromosome:
                  14:21022444 (GRCh38)
                  14:21490603 (GRCh37)
                  Canonical SPDI:
                  NC_000014.9:21022443:G:A,NC_000014.9:21022443:G:T
                  Gene:
                  NDRG2 (Varview), TPPP2 (Varview)
                  Functional Consequence:
                  coding_sequence_variant,upstream_transcript_variant,synonymous_variant,missense_variant,2KB_upstream_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  A=0.000062/2 (ALFA)
                  A=0.000004/1 (GnomAD_exomes)
                  T=0.000142/2 (TOMMO)
                  HGVS:
                  NC_000014.9:g.21022444G>A, NC_000014.9:g.21022444G>T, NC_000014.8:g.21490603G>A, NC_000014.8:g.21490603G>T, NM_016250.3:c.129C>T, NM_016250.3:c.129C>A, NM_016250.2:c.129C>T, NM_016250.2:c.129C>A, NM_001320329.2:c.171C>T, NM_001320329.2:c.171C>A, NM_001320329.1:c.171C>T, NM_001320329.1:c.171C>A, NM_001354565.2:c.171C>T, NM_001354565.2:c.171C>A, NM_001354565.1:c.171C>T, NM_001354565.1:c.171C>A, NM_001354568.2:c.129C>T, NM_001354568.2:c.129C>A, NM_001354568.1:c.129C>T, NM_001354568.1:c.129C>A, NM_001354570.2:c.171C>T, NM_001354570.2:c.171C>A, NM_001354570.1:c.171C>T, NM_001354570.1:c.171C>A, NM_001354567.2:c.171C>T, NM_001354567.2:c.171C>A, NM_001354567.1:c.171C>T, NM_001354567.1:c.171C>A, NM_001282212.2:c.129C>T, NM_001282212.2:c.129C>A, NM_001282212.1:c.129C>T, NM_001282212.1:c.129C>A, NM_001282214.2:c.129C>T, NM_001282214.2:c.129C>A, NM_001282214.1:c.129C>T, NM_001282214.1:c.129C>A, NM_001354561.2:c.129C>T, NM_001354561.2:c.129C>A, NM_001354561.1:c.129C>T, NM_001354561.1:c.129C>A, NM_001282213.2:c.129C>T, NM_001282213.2:c.129C>A, NM_001282213.1:c.129C>T, NM_001282213.1:c.129C>A, NM_001354559.2:c.171C>T, NM_001354559.2:c.171C>A, NM_001354559.1:c.171C>T, NM_001354559.1:c.171C>A, NM_201535.2:c.171C>T, NM_201535.2:c.171C>A, NM_201535.1:c.171C>T, NM_201535.1:c.171C>A, NM_001354562.2:c.171C>T, NM_001354562.2:c.171C>A, NM_001354562.1:c.171C>T, NM_001354562.1:c.171C>A, NM_201540.2:c.171C>T, NM_201540.2:c.171C>A, NM_201540.1:c.171C>T, NM_201540.1:c.171C>A, NM_001354558.2:c.171C>T, NM_001354558.2:c.171C>A, NM_001354558.1:c.171C>T, NM_001354558.1:c.171C>A, NM_201537.2:c.171C>T, NM_201537.2:c.171C>A, NM_201537.1:c.171C>T, NM_201537.1:c.171C>A, NM_201541.2:c.129C>T, NM_201541.2:c.129C>A, NM_201541.1:c.129C>T, NM_201541.1:c.129C>A, NM_001282215.2:c.171C>T, NM_001282215.2:c.171C>A, NM_001282215.1:c.171C>T, NM_001282215.1:c.171C>A, NM_201536.2:c.129C>T, NM_201536.2:c.129C>A, NM_201536.1:c.129C>T, NM_201536.1:c.129C>A, NM_201539.2:c.171C>T, NM_201539.2:c.171C>A, NM_201539.1:c.171C>T, NM_201539.1:c.171C>A, NM_001354564.2:c.171C>T, NM_001354564.2:c.171C>A, NM_001354564.1:c.171C>T, NM_001354564.1:c.171C>A, NM_001282211.2:c.159C>T, NM_001282211.2:c.159C>A, NM_001282211.1:c.159C>T, NM_001282211.1:c.159C>A, NM_201538.2:c.129C>T, NM_201538.2:c.129C>A, NM_201538.1:c.129C>T, NM_201538.1:c.129C>A, NM_001282216.2:c.8C>T, NM_001282216.2:c.8C>A, NM_001282216.1:c.8C>T, NM_001282216.1:c.8C>A, NM_001354560.2:c.129C>T, NM_001354560.2:c.129C>A, NM_001354560.1:c.129C>T, NM_001354560.1:c.129C>A, NM_001354569.1:c.129C>T, NM_001354569.1:c.129C>A, NM_001354566.1:c.171C>T, NM_001354566.1:c.171C>A, NP_001269145.1:p.Pro3Leu, NP_001269145.1:p.Pro3His

                  9.

                  rs1454117611 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    G>A [Show Flanks]
                    Chromosome:
                    14:21022164 (GRCh38)
                    14:21490323 (GRCh37)
                    Canonical SPDI:
                    NC_000014.9:21022163:G:A
                    Gene:
                    NDRG2 (Varview)
                    Functional Consequence:
                    coding_sequence_variant,missense_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_000014.9:g.21022164G>A, NC_000014.8:g.21490323G>A, NM_016250.3:c.200C>T, NM_016250.2:c.200C>T, NM_001320329.2:c.242C>T, NM_001320329.1:c.242C>T, NM_001354565.2:c.242C>T, NM_001354565.1:c.242C>T, NM_001354568.2:c.200C>T, NM_001354568.1:c.200C>T, NM_001354570.2:c.242C>T, NM_001354570.1:c.242C>T, NM_001354567.2:c.242C>T, NM_001354567.1:c.242C>T, NM_001282212.2:c.200C>T, NM_001282212.1:c.200C>T, NM_001282214.2:c.200C>T, NM_001282214.1:c.200C>T, NM_001354561.2:c.200C>T, NM_001354561.1:c.200C>T, NM_001282213.2:c.200C>T, NM_001282213.1:c.200C>T, NM_001354559.2:c.242C>T, NM_001354559.1:c.242C>T, NM_201535.2:c.242C>T, NM_201535.1:c.242C>T, NM_001354562.2:c.242C>T, NM_001354562.1:c.242C>T, NM_201540.2:c.242C>T, NM_201540.1:c.242C>T, NM_001354558.2:c.242C>T, NM_001354558.1:c.242C>T, NM_201537.2:c.242C>T, NM_201537.1:c.242C>T, NM_201541.2:c.200C>T, NM_201541.1:c.200C>T, NM_001282215.2:c.242C>T, NM_001282215.1:c.242C>T, NM_201536.2:c.200C>T, NM_201536.1:c.200C>T, NM_201539.2:c.242C>T, NM_201539.1:c.242C>T, NM_001354564.2:c.242C>T, NM_001354564.1:c.242C>T, NM_001282211.2:c.230C>T, NM_001282211.1:c.230C>T, NM_201538.2:c.200C>T, NM_201538.1:c.200C>T, NM_001282216.2:c.62C>T, NM_001282216.1:c.62C>T, NM_001354560.2:c.200C>T, NM_001354560.1:c.200C>T, NM_001354569.1:c.200C>T, NM_001354566.1:c.242C>T, NP_057334.1:p.Pro67Leu, NP_001307258.1:p.Pro81Leu, NP_001341494.1:p.Pro81Leu, NP_001341497.1:p.Pro67Leu, NP_001341499.1:p.Pro81Leu, NP_001341496.1:p.Pro81Leu, NP_001269141.1:p.Pro67Leu, NP_001269143.1:p.Pro67Leu, NP_001341490.1:p.Pro67Leu, NP_001269142.1:p.Pro67Leu, NP_001341488.1:p.Pro81Leu, NP_963293.1:p.Pro81Leu, NP_001341491.1:p.Pro81Leu, NP_963834.1:p.Pro81Leu, NP_001341487.1:p.Pro81Leu, NP_963831.1:p.Pro81Leu, NP_963835.1:p.Pro67Leu, NP_001269144.1:p.Pro81Leu, NP_963294.1:p.Pro67Leu, NP_963833.1:p.Pro81Leu, NP_001341493.1:p.Pro81Leu, NP_001269140.1:p.Pro77Leu, NP_963832.1:p.Pro67Leu, NP_001269145.1:p.Pro21Leu, NP_001341489.1:p.Pro67Leu, NP_001341498.1:p.Pro67Leu, NP_001341495.1:p.Pro81Leu

                    10.

                    rs1454075078 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      C>T [Show Flanks]
                      Chromosome:
                      14:21023292 (GRCh38)
                      14:21491451 (GRCh37)
                      Canonical SPDI:
                      NC_000014.9:21023291:C:T
                      Gene:
                      NDRG2 (Varview), TPPP2 (Varview), MIR6717 (Varview)
                      Functional Consequence:
                      5_prime_UTR_variant,coding_sequence_variant,500B_downstream_variant,upstream_transcript_variant,synonymous_variant,downstream_transcript_variant,2KB_upstream_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_000014.9:g.21023292C>T, NC_000014.8:g.21491451C>T, NM_016250.3:c.24G>A, NM_016250.2:c.24G>A, NM_001320329.2:c.24G>A, NM_001320329.1:c.24G>A, NM_001354565.2:c.24G>A, NM_001354565.1:c.24G>A, NM_001354568.2:c.24G>A, NM_001354568.1:c.24G>A, NM_001354570.2:c.24G>A, NM_001354570.1:c.24G>A, NM_001354567.2:c.24G>A, NM_001354567.1:c.24G>A, NM_001282212.2:c.24G>A, NM_001282212.1:c.24G>A, NM_001282214.2:c.24G>A, NM_001282214.1:c.24G>A, NM_001354561.2:c.24G>A, NM_001354561.1:c.24G>A, NM_001282213.2:c.24G>A, NM_001282213.1:c.24G>A, NM_001354559.2:c.24G>A, NM_001354559.1:c.24G>A, NM_201535.2:c.24G>A, NM_201535.1:c.24G>A, NM_001354562.2:c.24G>A, NM_001354562.1:c.24G>A, NM_201540.2:c.24G>A, NM_201540.1:c.24G>A, NM_001354558.2:c.24G>A, NM_001354558.1:c.24G>A, NM_201537.2:c.24G>A, NM_201537.1:c.24G>A, NM_201541.2:c.24G>A, NM_201541.1:c.24G>A, NM_001282215.2:c.24G>A, NM_001282215.1:c.24G>A, NM_201536.2:c.24G>A, NM_201536.1:c.24G>A, NM_201539.2:c.24G>A, NM_201539.1:c.24G>A, NM_001354564.2:c.24G>A, NM_001354564.1:c.24G>A, NM_001282211.2:c.54G>A, NM_001282211.1:c.54G>A, NM_201538.2:c.24G>A, NM_201538.1:c.24G>A, NM_001282216.2:c.-98G>A, NM_001282216.1:c.-98G>A, NM_001354560.2:c.24G>A, NM_001354560.1:c.24G>A, NM_001354569.1:c.24G>A, NM_001354566.1:c.24G>A

                      11.

                      rs1449383998 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        C>T [Show Flanks]
                        Chromosome:
                        14:21018789 (GRCh38)
                        14:21486948 (GRCh37)
                        Canonical SPDI:
                        NC_000014.9:21018788:C:T
                        Gene:
                        NDRG2 (Varview)
                        Functional Consequence:
                        intron_variant,coding_sequence_variant,missense_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        T=0./0 (ALFA)
                        T=0.000004/1 (GnomAD_exomes)
                        T=0.000007/1 (GnomAD)
                        HGVS:
                        NC_000014.9:g.21018789C>T, NC_000014.8:g.21486948C>T, NM_016250.3:c.745G>A, NM_016250.2:c.745G>A, NM_001320329.2:c.787G>A, NM_001320329.1:c.787G>A, NM_001354565.2:c.787G>A, NM_001354565.1:c.787G>A, NM_001354568.2:c.745G>A, NM_001354568.1:c.745G>A, NM_001354570.2:c.787G>A, NM_001354570.1:c.787G>A, NM_001354567.2:c.787G>A, NM_001354567.1:c.787G>A, NM_001282212.2:c.745G>A, NM_001282212.1:c.745G>A, NM_001282214.2:c.745G>A, NM_001282214.1:c.745G>A, NM_001354561.2:c.745G>A, NM_001354561.1:c.745G>A, NM_001282213.2:c.745G>A, NM_001282213.1:c.745G>A, NM_001354559.2:c.787G>A, NM_001354559.1:c.787G>A, NM_201535.2:c.787G>A, NM_201535.1:c.787G>A, NM_001354562.2:c.787G>A, NM_001354562.1:c.787G>A, NM_201540.2:c.787G>A, NM_201540.1:c.787G>A, NM_001354558.2:c.787G>A, NM_001354558.1:c.787G>A, NM_201537.2:c.787G>A, NM_201537.1:c.787G>A, NM_201541.2:c.745G>A, NM_201541.1:c.745G>A, NM_201536.2:c.745G>A, NM_201536.1:c.745G>A, NM_201539.2:c.787G>A, NM_201539.1:c.787G>A, NM_001354564.2:c.787G>A, NM_001354564.1:c.787G>A, NM_001282211.2:c.775G>A, NM_001282211.1:c.775G>A, NM_201538.2:c.745G>A, NM_201538.1:c.745G>A, NM_001282216.2:c.607G>A, NM_001282216.1:c.607G>A, NM_001354560.2:c.745G>A, NM_001354560.1:c.745G>A, NM_001354569.1:c.745G>A, NM_001354566.1:c.787G>A, NP_057334.1:p.Asp249Asn, NP_001307258.1:p.Asp263Asn, NP_001341494.1:p.Asp263Asn, NP_001341497.1:p.Asp249Asn, NP_001341499.1:p.Asp263Asn, NP_001341496.1:p.Asp263Asn, NP_001269141.1:p.Asp249Asn, NP_001269143.1:p.Asp249Asn, NP_001341490.1:p.Asp249Asn, NP_001269142.1:p.Asp249Asn, NP_001341488.1:p.Asp263Asn, NP_963293.1:p.Asp263Asn, NP_001341491.1:p.Asp263Asn, NP_963834.1:p.Asp263Asn, NP_001341487.1:p.Asp263Asn, NP_963831.1:p.Asp263Asn, NP_963835.1:p.Asp249Asn, NP_963294.1:p.Asp249Asn, NP_963833.1:p.Asp263Asn, NP_001341493.1:p.Asp263Asn, NP_001269140.1:p.Asp259Asn, NP_963832.1:p.Asp249Asn, NP_001269145.1:p.Asp203Asn, NP_001341489.1:p.Asp249Asn, NP_001341498.1:p.Asp249Asn, NP_001341495.1:p.Asp263Asn

                        12.

                        rs1446843001 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          G>A [Show Flanks]
                          Chromosome:
                          14:21021868 (GRCh38)
                          14:21490027 (GRCh37)
                          Canonical SPDI:
                          NC_000014.9:21021867:G:A
                          Gene:
                          NDRG2 (Varview)
                          Functional Consequence:
                          coding_sequence_variant,missense_variant
                          HGVS:
                          NC_000014.9:g.21021868G>A, NC_000014.8:g.21490027G>A, NM_016250.3:c.314C>T, NM_016250.2:c.314C>T, NM_001320329.2:c.356C>T, NM_001320329.1:c.356C>T, NM_001354565.2:c.356C>T, NM_001354565.1:c.356C>T, NM_001354568.2:c.314C>T, NM_001354568.1:c.314C>T, NM_001354570.2:c.356C>T, NM_001354570.1:c.356C>T, NM_001354567.2:c.356C>T, NM_001354567.1:c.356C>T, NM_001282212.2:c.314C>T, NM_001282212.1:c.314C>T, NM_001282214.2:c.314C>T, NM_001282214.1:c.314C>T, NM_001354561.2:c.314C>T, NM_001354561.1:c.314C>T, NM_001282213.2:c.314C>T, NM_001282213.1:c.314C>T, NM_001354559.2:c.356C>T, NM_001354559.1:c.356C>T, NM_201535.2:c.356C>T, NM_201535.1:c.356C>T, NM_001354562.2:c.356C>T, NM_001354562.1:c.356C>T, NM_201540.2:c.356C>T, NM_201540.1:c.356C>T, NM_001354558.2:c.356C>T, NM_001354558.1:c.356C>T, NM_201537.2:c.356C>T, NM_201537.1:c.356C>T, NM_201541.2:c.314C>T, NM_201541.1:c.314C>T, NM_001282215.2:c.356C>T, NM_001282215.1:c.356C>T, NM_201536.2:c.314C>T, NM_201536.1:c.314C>T, NM_201539.2:c.356C>T, NM_201539.1:c.356C>T, NM_001354564.2:c.356C>T, NM_001354564.1:c.356C>T, NM_001282211.2:c.344C>T, NM_001282211.1:c.344C>T, NM_201538.2:c.314C>T, NM_201538.1:c.314C>T, NM_001282216.2:c.176C>T, NM_001282216.1:c.176C>T, NM_001354560.2:c.314C>T, NM_001354560.1:c.314C>T, NM_001354569.1:c.314C>T, NM_001354566.1:c.356C>T, NP_057334.1:p.Pro105Leu, NP_001307258.1:p.Pro119Leu, NP_001341494.1:p.Pro119Leu, NP_001341497.1:p.Pro105Leu, NP_001341499.1:p.Pro119Leu, NP_001341496.1:p.Pro119Leu, NP_001269141.1:p.Pro105Leu, NP_001269143.1:p.Pro105Leu, NP_001341490.1:p.Pro105Leu, NP_001269142.1:p.Pro105Leu, NP_001341488.1:p.Pro119Leu, NP_963293.1:p.Pro119Leu, NP_001341491.1:p.Pro119Leu, NP_963834.1:p.Pro119Leu, NP_001341487.1:p.Pro119Leu, NP_963831.1:p.Pro119Leu, NP_963835.1:p.Pro105Leu, NP_001269144.1:p.Pro119Leu, NP_963294.1:p.Pro105Leu, NP_963833.1:p.Pro119Leu, NP_001341493.1:p.Pro119Leu, NP_001269140.1:p.Pro115Leu, NP_963832.1:p.Pro105Leu, NP_001269145.1:p.Pro59Leu, NP_001341489.1:p.Pro105Leu, NP_001341498.1:p.Pro105Leu, NP_001341495.1:p.Pro119Leu

                          13.

                          rs1446725846 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            G>A,C [Show Flanks]
                            Chromosome:
                            14:21019712 (GRCh38)
                            14:21487871 (GRCh37)
                            Canonical SPDI:
                            NC_000014.9:21019711:G:A,NC_000014.9:21019711:G:C
                            Gene:
                            NDRG2 (Varview)
                            Functional Consequence:
                            coding_sequence_variant,missense_variant,stop_gained
                            HGVS:
                            NC_000014.9:g.21019712G>A, NC_000014.9:g.21019712G>C, NC_000014.8:g.21487871G>A, NC_000014.8:g.21487871G>C, NM_016250.3:c.601C>T, NM_016250.3:c.601C>G, NM_016250.2:c.601C>T, NM_016250.2:c.601C>G, NM_001320329.2:c.643C>T, NM_001320329.2:c.643C>G, NM_001320329.1:c.643C>T, NM_001320329.1:c.643C>G, NM_001354565.2:c.643C>T, NM_001354565.2:c.643C>G, NM_001354565.1:c.643C>T, NM_001354565.1:c.643C>G, NM_001354568.2:c.601C>T, NM_001354568.2:c.601C>G, NM_001354568.1:c.601C>T, NM_001354568.1:c.601C>G, NM_001354570.2:c.643C>T, NM_001354570.2:c.643C>G, NM_001354570.1:c.643C>T, NM_001354570.1:c.643C>G, NM_001354567.2:c.643C>T, NM_001354567.2:c.643C>G, NM_001354567.1:c.643C>T, NM_001354567.1:c.643C>G, NM_001282212.2:c.601C>T, NM_001282212.2:c.601C>G, NM_001282212.1:c.601C>T, NM_001282212.1:c.601C>G, NM_001282214.2:c.601C>T, NM_001282214.2:c.601C>G, NM_001282214.1:c.601C>T, NM_001282214.1:c.601C>G, NM_001354561.2:c.601C>T, NM_001354561.2:c.601C>G, NM_001354561.1:c.601C>T, NM_001354561.1:c.601C>G, NM_001282213.2:c.601C>T, NM_001282213.2:c.601C>G, NM_001282213.1:c.601C>T, NM_001282213.1:c.601C>G, NM_001354559.2:c.643C>T, NM_001354559.2:c.643C>G, NM_001354559.1:c.643C>T, NM_001354559.1:c.643C>G, NM_201535.2:c.643C>T, NM_201535.2:c.643C>G, NM_201535.1:c.643C>T, NM_201535.1:c.643C>G, NM_001354562.2:c.643C>T, NM_001354562.2:c.643C>G, NM_001354562.1:c.643C>T, NM_001354562.1:c.643C>G, NM_201540.2:c.643C>T, NM_201540.2:c.643C>G, NM_201540.1:c.643C>T, NM_201540.1:c.643C>G, NM_001354558.2:c.643C>T, NM_001354558.2:c.643C>G, NM_001354558.1:c.643C>T, NM_001354558.1:c.643C>G, NM_201537.2:c.643C>T, NM_201537.2:c.643C>G, NM_201537.1:c.643C>T, NM_201537.1:c.643C>G, NM_201541.2:c.601C>T, NM_201541.2:c.601C>G, NM_201541.1:c.601C>T, NM_201541.1:c.601C>G, NM_001282215.2:c.643C>T, NM_001282215.2:c.643C>G, NM_001282215.1:c.643C>T, NM_001282215.1:c.643C>G, NM_201536.2:c.601C>T, NM_201536.2:c.601C>G, NM_201536.1:c.601C>T, NM_201536.1:c.601C>G, NM_201539.2:c.643C>T, NM_201539.2:c.643C>G, NM_201539.1:c.643C>T, NM_201539.1:c.643C>G, NM_001354564.2:c.643C>T, NM_001354564.2:c.643C>G, NM_001354564.1:c.643C>T, NM_001354564.1:c.643C>G, NM_001282211.2:c.631C>T, NM_001282211.2:c.631C>G, NM_001282211.1:c.631C>T, NM_001282211.1:c.631C>G, NM_201538.2:c.601C>T, NM_201538.2:c.601C>G, NM_201538.1:c.601C>T, NM_201538.1:c.601C>G, NM_001282216.2:c.463C>T, NM_001282216.2:c.463C>G, NM_001282216.1:c.463C>T, NM_001282216.1:c.463C>G, NM_001354560.2:c.601C>T, NM_001354560.2:c.601C>G, NM_001354560.1:c.601C>T, NM_001354560.1:c.601C>G, NM_001354569.1:c.601C>T, NM_001354569.1:c.601C>G, NM_001354566.1:c.643C>T, NM_001354566.1:c.643C>G, NP_057334.1:p.Gln201Ter, NP_057334.1:p.Gln201Glu, NP_001307258.1:p.Gln215Ter, NP_001307258.1:p.Gln215Glu, NP_001341494.1:p.Gln215Ter, NP_001341494.1:p.Gln215Glu, NP_001341497.1:p.Gln201Ter, NP_001341497.1:p.Gln201Glu, NP_001341499.1:p.Gln215Ter, NP_001341499.1:p.Gln215Glu, NP_001341496.1:p.Gln215Ter, NP_001341496.1:p.Gln215Glu, NP_001269141.1:p.Gln201Ter, NP_001269141.1:p.Gln201Glu, NP_001269143.1:p.Gln201Ter, NP_001269143.1:p.Gln201Glu, NP_001341490.1:p.Gln201Ter, NP_001341490.1:p.Gln201Glu, NP_001269142.1:p.Gln201Ter, NP_001269142.1:p.Gln201Glu, NP_001341488.1:p.Gln215Ter, NP_001341488.1:p.Gln215Glu, NP_963293.1:p.Gln215Ter, NP_963293.1:p.Gln215Glu, NP_001341491.1:p.Gln215Ter, NP_001341491.1:p.Gln215Glu, NP_963834.1:p.Gln215Ter, NP_963834.1:p.Gln215Glu, NP_001341487.1:p.Gln215Ter, NP_001341487.1:p.Gln215Glu, NP_963831.1:p.Gln215Ter, NP_963831.1:p.Gln215Glu, NP_963835.1:p.Gln201Ter, NP_963835.1:p.Gln201Glu, NP_001269144.1:p.Gln215Ter, NP_001269144.1:p.Gln215Glu, NP_963294.1:p.Gln201Ter, NP_963294.1:p.Gln201Glu, NP_963833.1:p.Gln215Ter, NP_963833.1:p.Gln215Glu, NP_001341493.1:p.Gln215Ter, NP_001341493.1:p.Gln215Glu, NP_001269140.1:p.Gln211Ter, NP_001269140.1:p.Gln211Glu, NP_963832.1:p.Gln201Ter, NP_963832.1:p.Gln201Glu, NP_001269145.1:p.Gln155Ter, NP_001269145.1:p.Gln155Glu, NP_001341489.1:p.Gln201Ter, NP_001341489.1:p.Gln201Glu, NP_001341498.1:p.Gln201Ter, NP_001341498.1:p.Gln201Glu, NP_001341495.1:p.Gln215Ter, NP_001341495.1:p.Gln215Glu

                            14.

                            rs1444235304 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              T>G [Show Flanks]
                              Chromosome:
                              14:21022433 (GRCh38)
                              14:21490592 (GRCh37)
                              Canonical SPDI:
                              NC_000014.9:21022432:T:G
                              Gene:
                              NDRG2 (Varview), TPPP2 (Varview)
                              Functional Consequence:
                              upstream_transcript_variant,coding_sequence_variant,missense_variant,2KB_upstream_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              G=0./0 (ALFA)
                              G=0.000012/3 (GnomAD_exomes)
                              G=0.000015/4 (TOPMED)
                              HGVS:
                              NC_000014.9:g.21022433T>G, NC_000014.8:g.21490592T>G, NM_016250.3:c.140A>C, NM_016250.2:c.140A>C, NM_001320329.2:c.182A>C, NM_001320329.1:c.182A>C, NM_001354565.2:c.182A>C, NM_001354565.1:c.182A>C, NM_001354568.2:c.140A>C, NM_001354568.1:c.140A>C, NM_001354570.2:c.182A>C, NM_001354570.1:c.182A>C, NM_001354567.2:c.182A>C, NM_001354567.1:c.182A>C, NM_001282212.2:c.140A>C, NM_001282212.1:c.140A>C, NM_001282214.2:c.140A>C, NM_001282214.1:c.140A>C, NM_001354561.2:c.140A>C, NM_001354561.1:c.140A>C, NM_001282213.2:c.140A>C, NM_001282213.1:c.140A>C, NM_001354559.2:c.182A>C, NM_001354559.1:c.182A>C, NM_201535.2:c.182A>C, NM_201535.1:c.182A>C, NM_001354562.2:c.182A>C, NM_001354562.1:c.182A>C, NM_201540.2:c.182A>C, NM_201540.1:c.182A>C, NM_001354558.2:c.182A>C, NM_001354558.1:c.182A>C, NM_201537.2:c.182A>C, NM_201537.1:c.182A>C, NM_201541.2:c.140A>C, NM_201541.1:c.140A>C, NM_001282215.2:c.182A>C, NM_001282215.1:c.182A>C, NM_201536.2:c.140A>C, NM_201536.1:c.140A>C, NM_201539.2:c.182A>C, NM_201539.1:c.182A>C, NM_001354564.2:c.182A>C, NM_001354564.1:c.182A>C, NM_001282211.2:c.170A>C, NM_001282211.1:c.170A>C, NM_201538.2:c.140A>C, NM_201538.1:c.140A>C, NM_001282216.2:c.19A>C, NM_001282216.1:c.19A>C, NM_001354560.2:c.140A>C, NM_001354560.1:c.140A>C, NM_001354569.1:c.140A>C, NM_001354566.1:c.182A>C, NP_057334.1:p.Lys47Thr, NP_001307258.1:p.Lys61Thr, NP_001341494.1:p.Lys61Thr, NP_001341497.1:p.Lys47Thr, NP_001341499.1:p.Lys61Thr, NP_001341496.1:p.Lys61Thr, NP_001269141.1:p.Lys47Thr, NP_001269143.1:p.Lys47Thr, NP_001341490.1:p.Lys47Thr, NP_001269142.1:p.Lys47Thr, NP_001341488.1:p.Lys61Thr, NP_963293.1:p.Lys61Thr, NP_001341491.1:p.Lys61Thr, NP_963834.1:p.Lys61Thr, NP_001341487.1:p.Lys61Thr, NP_963831.1:p.Lys61Thr, NP_963835.1:p.Lys47Thr, NP_001269144.1:p.Lys61Thr, NP_963294.1:p.Lys47Thr, NP_963833.1:p.Lys61Thr, NP_001341493.1:p.Lys61Thr, NP_001269140.1:p.Lys57Thr, NP_963832.1:p.Lys47Thr, NP_001269145.1:p.Asn7His, NP_001341489.1:p.Lys47Thr, NP_001341498.1:p.Lys47Thr, NP_001341495.1:p.Lys61Thr

                              15.

                              rs1442070768 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                C>T [Show Flanks]
                                Chromosome:
                                14:21018504 (GRCh38)
                                14:21486663 (GRCh37)
                                Canonical SPDI:
                                NC_000014.9:21018503:C:T
                                Gene:
                                NDRG2 (Varview)
                                Functional Consequence:
                                intron_variant,coding_sequence_variant,missense_variant
                                HGVS:
                                NC_000014.9:g.21018504C>T, NC_000014.8:g.21486663C>T, NM_016250.3:c.772G>A, NM_016250.2:c.772G>A, NM_001320329.2:c.814G>A, NM_001320329.1:c.814G>A, NM_001354565.2:c.814G>A, NM_001354565.1:c.814G>A, NM_001354568.2:c.772G>A, NM_001354568.1:c.772G>A, NM_001354570.2:c.814G>A, NM_001354570.1:c.814G>A, NM_001354567.2:c.814G>A, NM_001354567.1:c.814G>A, NM_001282214.2:c.772G>A, NM_001282214.1:c.772G>A, NM_001354561.2:c.772G>A, NM_001354561.1:c.772G>A, NM_001282213.2:c.772G>A, NM_001282213.1:c.772G>A, NM_001354559.2:c.814G>A, NM_001354559.1:c.814G>A, NM_201535.2:c.814G>A, NM_201535.1:c.814G>A, NM_001354562.2:c.814G>A, NM_001354562.1:c.814G>A, NM_201540.2:c.814G>A, NM_201540.1:c.814G>A, NM_001354558.2:c.868G>A, NM_001354558.1:c.868G>A, NM_201537.2:c.814G>A, NM_201537.1:c.814G>A, NM_201541.2:c.772G>A, NM_201541.1:c.772G>A, NM_001282215.2:c.781G>A, NM_001282215.1:c.781G>A, NM_201536.2:c.772G>A, NM_201536.1:c.772G>A, NM_201539.2:c.814G>A, NM_201539.1:c.814G>A, NM_001354564.2:c.814G>A, NM_001354564.1:c.814G>A, NM_001282211.2:c.802G>A, NM_001282211.1:c.802G>A, NM_201538.2:c.772G>A, NM_201538.1:c.772G>A, NM_001282216.2:c.634G>A, NM_001282216.1:c.634G>A, NM_001354569.1:c.772G>A, NM_001354566.1:c.814G>A, NP_057334.1:p.Val258Met, NP_001307258.1:p.Val272Met, NP_001341494.1:p.Val272Met, NP_001341497.1:p.Val258Met, NP_001341499.1:p.Val272Met, NP_001341496.1:p.Val272Met, NP_001269143.1:p.Val258Met, NP_001341490.1:p.Val258Met, NP_001269142.1:p.Val258Met, NP_001341488.1:p.Val272Met, NP_963293.1:p.Val272Met, NP_001341491.1:p.Val272Met, NP_963834.1:p.Val272Met, NP_001341487.1:p.Val290Met, NP_963831.1:p.Val272Met, NP_963835.1:p.Val258Met, NP_001269144.1:p.Val261Met, NP_963294.1:p.Val258Met, NP_963833.1:p.Val272Met, NP_001341493.1:p.Val272Met, NP_001269140.1:p.Val268Met, NP_963832.1:p.Val258Met, NP_001269145.1:p.Val212Met, NP_001341498.1:p.Val258Met, NP_001341495.1:p.Val272Met

                                16.

                                rs1441534985 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  C>T [Show Flanks]
                                  Chromosome:
                                  14:21017683 (GRCh38)
                                  14:21485842 (GRCh37)
                                  Canonical SPDI:
                                  NC_000014.9:21017682:C:T
                                  Gene:
                                  NDRG2 (Varview)
                                  Functional Consequence:
                                  coding_sequence_variant,3_prime_UTR_variant,synonymous_variant
                                  Validated:
                                  by frequency
                                  MAF:
                                  T=0.000004/1 (GnomAD_exomes)
                                  HGVS:
                                  NC_000014.9:g.21017683C>T, NC_000014.8:g.21485842C>T, NM_016250.3:c.987G>A, NM_016250.2:c.987G>A, NM_001320329.2:c.1029G>A, NM_001320329.1:c.1029G>A, NM_001354565.2:c.1029G>A, NM_001354565.1:c.1029G>A, NM_001354568.2:c.987G>A, NM_001354568.1:c.987G>A, NM_001354570.2:c.1029G>A, NM_001354570.1:c.1029G>A, NM_001354567.2:c.1029G>A, NM_001354567.1:c.1029G>A, NM_001282212.2:c.939G>A, NM_001282212.1:c.939G>A, NM_001282214.2:c.987G>A, NM_001282214.1:c.987G>A, NM_001354561.2:c.987G>A, NM_001354561.1:c.987G>A, NM_001282213.2:c.987G>A, NM_001282213.1:c.987G>A, NM_001354559.2:c.1029G>A, NM_001354559.1:c.1029G>A, NM_201535.2:c.1029G>A, NM_201535.1:c.1029G>A, NM_001354562.2:c.1029G>A, NM_001354562.1:c.1029G>A, NM_201540.2:c.1029G>A, NM_201540.1:c.1029G>A, NM_001354558.2:c.1083G>A, NM_001354558.1:c.1083G>A, NM_201537.2:c.1029G>A, NM_201537.1:c.1029G>A, NM_201541.2:c.987G>A, NM_201541.1:c.987G>A, NM_001282215.2:c.996G>A, NM_001282215.1:c.996G>A, NM_201536.2:c.987G>A, NM_201536.1:c.987G>A, NM_201539.2:c.1029G>A, NM_201539.1:c.1029G>A, NM_001354564.2:c.*119G>A, NM_001354564.1:c.*119G>A, NM_001282211.2:c.1017G>A, NM_001282211.1:c.1017G>A, NM_201538.2:c.987G>A, NM_201538.1:c.987G>A, NM_001282216.2:c.849G>A, NM_001282216.1:c.849G>A, NM_001354560.2:c.954G>A, NM_001354560.1:c.954G>A, NM_001354569.1:c.987G>A, NM_001354566.1:c.1029G>A

                                  17.

                                  rs1441110957 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    G>A,C [Show Flanks]
                                    Chromosome:
                                    14:21020501 (GRCh38)
                                    14:21488660 (GRCh37)
                                    Canonical SPDI:
                                    NC_000014.9:21020500:G:A,NC_000014.9:21020500:G:C
                                    Gene:
                                    NDRG2 (Varview)
                                    Functional Consequence:
                                    coding_sequence_variant,missense_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    C=0./0 (ALFA)
                                    C=0.000007/1 (GnomAD)
                                    HGVS:
                                    NC_000014.9:g.21020501G>A, NC_000014.9:g.21020501G>C, NC_000014.8:g.21488660G>A, NC_000014.8:g.21488660G>C, NM_016250.3:c.508C>T, NM_016250.3:c.508C>G, NM_016250.2:c.508C>T, NM_016250.2:c.508C>G, NM_001320329.2:c.550C>T, NM_001320329.2:c.550C>G, NM_001320329.1:c.550C>T, NM_001320329.1:c.550C>G, NM_001354565.2:c.550C>T, NM_001354565.2:c.550C>G, NM_001354565.1:c.550C>T, NM_001354565.1:c.550C>G, NM_001354568.2:c.508C>T, NM_001354568.2:c.508C>G, NM_001354568.1:c.508C>T, NM_001354568.1:c.508C>G, NM_001354570.2:c.550C>T, NM_001354570.2:c.550C>G, NM_001354570.1:c.550C>T, NM_001354570.1:c.550C>G, NM_001354567.2:c.550C>T, NM_001354567.2:c.550C>G, NM_001354567.1:c.550C>T, NM_001354567.1:c.550C>G, NM_001282212.2:c.508C>T, NM_001282212.2:c.508C>G, NM_001282212.1:c.508C>T, NM_001282212.1:c.508C>G, NM_001282214.2:c.508C>T, NM_001282214.2:c.508C>G, NM_001282214.1:c.508C>T, NM_001282214.1:c.508C>G, NM_001354561.2:c.508C>T, NM_001354561.2:c.508C>G, NM_001354561.1:c.508C>T, NM_001354561.1:c.508C>G, NM_001282213.2:c.508C>T, NM_001282213.2:c.508C>G, NM_001282213.1:c.508C>T, NM_001282213.1:c.508C>G, NM_001354559.2:c.550C>T, NM_001354559.2:c.550C>G, NM_001354559.1:c.550C>T, NM_001354559.1:c.550C>G, NM_201535.2:c.550C>T, NM_201535.2:c.550C>G, NM_201535.1:c.550C>T, NM_201535.1:c.550C>G, NM_001354562.2:c.550C>T, NM_001354562.2:c.550C>G, NM_001354562.1:c.550C>T, NM_001354562.1:c.550C>G, NM_201540.2:c.550C>T, NM_201540.2:c.550C>G, NM_201540.1:c.550C>T, NM_201540.1:c.550C>G, NM_001354558.2:c.550C>T, NM_001354558.2:c.550C>G, NM_001354558.1:c.550C>T, NM_001354558.1:c.550C>G, NM_201537.2:c.550C>T, NM_201537.2:c.550C>G, NM_201537.1:c.550C>T, NM_201537.1:c.550C>G, NM_201541.2:c.508C>T, NM_201541.2:c.508C>G, NM_201541.1:c.508C>T, NM_201541.1:c.508C>G, NM_001282215.2:c.550C>T, NM_001282215.2:c.550C>G, NM_001282215.1:c.550C>T, NM_001282215.1:c.550C>G, NM_201536.2:c.508C>T, NM_201536.2:c.508C>G, NM_201536.1:c.508C>T, NM_201536.1:c.508C>G, NM_201539.2:c.550C>T, NM_201539.2:c.550C>G, NM_201539.1:c.550C>T, NM_201539.1:c.550C>G, NM_001354564.2:c.550C>T, NM_001354564.2:c.550C>G, NM_001354564.1:c.550C>T, NM_001354564.1:c.550C>G, NM_001282211.2:c.538C>T, NM_001282211.2:c.538C>G, NM_001282211.1:c.538C>T, NM_001282211.1:c.538C>G, NM_201538.2:c.508C>T, NM_201538.2:c.508C>G, NM_201538.1:c.508C>T, NM_201538.1:c.508C>G, NM_001282216.2:c.370C>T, NM_001282216.2:c.370C>G, NM_001282216.1:c.370C>T, NM_001282216.1:c.370C>G, NM_001354560.2:c.508C>T, NM_001354560.2:c.508C>G, NM_001354560.1:c.508C>T, NM_001354560.1:c.508C>G, NM_001354569.1:c.508C>T, NM_001354569.1:c.508C>G, NM_001354566.1:c.550C>T, NM_001354566.1:c.550C>G, NP_057334.1:p.His170Tyr, NP_057334.1:p.His170Asp, NP_001307258.1:p.His184Tyr, NP_001307258.1:p.His184Asp, NP_001341494.1:p.His184Tyr, NP_001341494.1:p.His184Asp, NP_001341497.1:p.His170Tyr, NP_001341497.1:p.His170Asp, NP_001341499.1:p.His184Tyr, NP_001341499.1:p.His184Asp, NP_001341496.1:p.His184Tyr, NP_001341496.1:p.His184Asp, NP_001269141.1:p.His170Tyr, NP_001269141.1:p.His170Asp, NP_001269143.1:p.His170Tyr, NP_001269143.1:p.His170Asp, NP_001341490.1:p.His170Tyr, NP_001341490.1:p.His170Asp, NP_001269142.1:p.His170Tyr, NP_001269142.1:p.His170Asp, NP_001341488.1:p.His184Tyr, NP_001341488.1:p.His184Asp, NP_963293.1:p.His184Tyr, NP_963293.1:p.His184Asp, NP_001341491.1:p.His184Tyr, NP_001341491.1:p.His184Asp, NP_963834.1:p.His184Tyr, NP_963834.1:p.His184Asp, NP_001341487.1:p.His184Tyr, NP_001341487.1:p.His184Asp, NP_963831.1:p.His184Tyr, NP_963831.1:p.His184Asp, NP_963835.1:p.His170Tyr, NP_963835.1:p.His170Asp, NP_001269144.1:p.His184Tyr, NP_001269144.1:p.His184Asp, NP_963294.1:p.His170Tyr, NP_963294.1:p.His170Asp, NP_963833.1:p.His184Tyr, NP_963833.1:p.His184Asp, NP_001341493.1:p.His184Tyr, NP_001341493.1:p.His184Asp, NP_001269140.1:p.His180Tyr, NP_001269140.1:p.His180Asp, NP_963832.1:p.His170Tyr, NP_963832.1:p.His170Asp, NP_001269145.1:p.His124Tyr, NP_001269145.1:p.His124Asp, NP_001341489.1:p.His170Tyr, NP_001341489.1:p.His170Asp, NP_001341498.1:p.His170Tyr, NP_001341498.1:p.His170Asp, NP_001341495.1:p.His184Tyr, NP_001341495.1:p.His184Asp

                                    18.

                                    rs1441005230 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      G>C,T [Show Flanks]
                                      Chromosome:
                                      14:21018491 (GRCh38)
                                      14:21486650 (GRCh37)
                                      Canonical SPDI:
                                      NC_000014.9:21018490:G:C,NC_000014.9:21018490:G:T
                                      Gene:
                                      NDRG2 (Varview)
                                      Functional Consequence:
                                      intron_variant,coding_sequence_variant,stop_gained
                                      Validated:
                                      by frequency,by cluster
                                      MAF:
                                      T=0.000004/1 (GnomAD_exomes)
                                      C=0.000035/1 (TOMMO)
                                      HGVS:
                                      NC_000014.9:g.21018491G>C, NC_000014.9:g.21018491G>T, NC_000014.8:g.21486650G>C, NC_000014.8:g.21486650G>T, NM_016250.3:c.785C>G, NM_016250.3:c.785C>A, NM_016250.2:c.785C>G, NM_016250.2:c.785C>A, NM_001320329.2:c.827C>G, NM_001320329.2:c.827C>A, NM_001320329.1:c.827C>G, NM_001320329.1:c.827C>A, NM_001354565.2:c.827C>G, NM_001354565.2:c.827C>A, NM_001354565.1:c.827C>G, NM_001354565.1:c.827C>A, NM_001354568.2:c.785C>G, NM_001354568.2:c.785C>A, NM_001354568.1:c.785C>G, NM_001354568.1:c.785C>A, NM_001354570.2:c.827C>G, NM_001354570.2:c.827C>A, NM_001354570.1:c.827C>G, NM_001354570.1:c.827C>A, NM_001354567.2:c.827C>G, NM_001354567.2:c.827C>A, NM_001354567.1:c.827C>G, NM_001354567.1:c.827C>A, NM_001282214.2:c.785C>G, NM_001282214.2:c.785C>A, NM_001282214.1:c.785C>G, NM_001282214.1:c.785C>A, NM_001354561.2:c.785C>G, NM_001354561.2:c.785C>A, NM_001354561.1:c.785C>G, NM_001354561.1:c.785C>A, NM_001282213.2:c.785C>G, NM_001282213.2:c.785C>A, NM_001282213.1:c.785C>G, NM_001282213.1:c.785C>A, NM_001354559.2:c.827C>G, NM_001354559.2:c.827C>A, NM_001354559.1:c.827C>G, NM_001354559.1:c.827C>A, NM_201535.2:c.827C>G, NM_201535.2:c.827C>A, NM_201535.1:c.827C>G, NM_201535.1:c.827C>A, NM_001354562.2:c.827C>G, NM_001354562.2:c.827C>A, NM_001354562.1:c.827C>G, NM_001354562.1:c.827C>A, NM_201540.2:c.827C>G, NM_201540.2:c.827C>A, NM_201540.1:c.827C>G, NM_201540.1:c.827C>A, NM_001354558.2:c.881C>G, NM_001354558.2:c.881C>A, NM_001354558.1:c.881C>G, NM_001354558.1:c.881C>A, NM_201537.2:c.827C>G, NM_201537.2:c.827C>A, NM_201537.1:c.827C>G, NM_201537.1:c.827C>A, NM_201541.2:c.785C>G, NM_201541.2:c.785C>A, NM_201541.1:c.785C>G, NM_201541.1:c.785C>A, NM_001282215.2:c.794C>G, NM_001282215.2:c.794C>A, NM_001282215.1:c.794C>G, NM_001282215.1:c.794C>A, NM_201536.2:c.785C>G, NM_201536.2:c.785C>A, NM_201536.1:c.785C>G, NM_201536.1:c.785C>A, NM_201539.2:c.827C>G, NM_201539.2:c.827C>A, NM_201539.1:c.827C>G, NM_201539.1:c.827C>A, NM_001354564.2:c.827C>G, NM_001354564.2:c.827C>A, NM_001354564.1:c.827C>G, NM_001354564.1:c.827C>A, NM_001282211.2:c.815C>G, NM_001282211.2:c.815C>A, NM_001282211.1:c.815C>G, NM_001282211.1:c.815C>A, NM_201538.2:c.785C>G, NM_201538.2:c.785C>A, NM_201538.1:c.785C>G, NM_201538.1:c.785C>A, NM_001282216.2:c.647C>G, NM_001282216.2:c.647C>A, NM_001282216.1:c.647C>G, NM_001282216.1:c.647C>A, NM_001354569.1:c.785C>G, NM_001354569.1:c.785C>A, NM_001354566.1:c.827C>G, NM_001354566.1:c.827C>A, NP_057334.1:p.Ser262Ter, NP_057334.1:p.Ser262Ter, NP_001307258.1:p.Ser276Ter, NP_001307258.1:p.Ser276Ter, NP_001341494.1:p.Ser276Ter, NP_001341494.1:p.Ser276Ter, NP_001341497.1:p.Ser262Ter, NP_001341497.1:p.Ser262Ter, NP_001341499.1:p.Ser276Ter, NP_001341499.1:p.Ser276Ter, NP_001341496.1:p.Ser276Ter, NP_001341496.1:p.Ser276Ter, NP_001269143.1:p.Ser262Ter, NP_001269143.1:p.Ser262Ter, NP_001341490.1:p.Ser262Ter, NP_001341490.1:p.Ser262Ter, NP_001269142.1:p.Ser262Ter, NP_001269142.1:p.Ser262Ter, NP_001341488.1:p.Ser276Ter, NP_001341488.1:p.Ser276Ter, NP_963293.1:p.Ser276Ter, NP_963293.1:p.Ser276Ter, NP_001341491.1:p.Ser276Ter, NP_001341491.1:p.Ser276Ter, NP_963834.1:p.Ser276Ter, NP_963834.1:p.Ser276Ter, NP_001341487.1:p.Ser294Ter, NP_001341487.1:p.Ser294Ter, NP_963831.1:p.Ser276Ter, NP_963831.1:p.Ser276Ter, NP_963835.1:p.Ser262Ter, NP_963835.1:p.Ser262Ter, NP_001269144.1:p.Ser265Ter, NP_001269144.1:p.Ser265Ter, NP_963294.1:p.Ser262Ter, NP_963294.1:p.Ser262Ter, NP_963833.1:p.Ser276Ter, NP_963833.1:p.Ser276Ter, NP_001341493.1:p.Ser276Ter, NP_001341493.1:p.Ser276Ter, NP_001269140.1:p.Ser272Ter, NP_001269140.1:p.Ser272Ter, NP_963832.1:p.Ser262Ter, NP_963832.1:p.Ser262Ter, NP_001269145.1:p.Ser216Ter, NP_001269145.1:p.Ser216Ter, NP_001341498.1:p.Ser262Ter, NP_001341498.1:p.Ser262Ter, NP_001341495.1:p.Ser276Ter, NP_001341495.1:p.Ser276Ter

                                      19.

                                      rs1437469417 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        C>G,T [Show Flanks]
                                        Chromosome:
                                        14:21022081 (GRCh38)
                                        14:21490240 (GRCh37)
                                        Canonical SPDI:
                                        NC_000014.9:21022080:C:G,NC_000014.9:21022080:C:T
                                        Gene:
                                        NDRG2 (Varview)
                                        Functional Consequence:
                                        coding_sequence_variant,missense_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        G=0./0 (ALFA)
                                        T=0.000004/1 (GnomAD_exomes)
                                        G=0.000008/2 (TOPMED)
                                        HGVS:
                                        NC_000014.9:g.21022081C>G, NC_000014.9:g.21022081C>T, NC_000014.8:g.21490240C>G, NC_000014.8:g.21490240C>T, NM_016250.3:c.283G>C, NM_016250.3:c.283G>A, NM_016250.2:c.283G>C, NM_016250.2:c.283G>A, NM_001320329.2:c.325G>C, NM_001320329.2:c.325G>A, NM_001320329.1:c.325G>C, NM_001320329.1:c.325G>A, NM_001354565.2:c.325G>C, NM_001354565.2:c.325G>A, NM_001354565.1:c.325G>C, NM_001354565.1:c.325G>A, NM_001354568.2:c.283G>C, NM_001354568.2:c.283G>A, NM_001354568.1:c.283G>C, NM_001354568.1:c.283G>A, NM_001354570.2:c.325G>C, NM_001354570.2:c.325G>A, NM_001354570.1:c.325G>C, NM_001354570.1:c.325G>A, NM_001354567.2:c.325G>C, NM_001354567.2:c.325G>A, NM_001354567.1:c.325G>C, NM_001354567.1:c.325G>A, NM_001282212.2:c.283G>C, NM_001282212.2:c.283G>A, NM_001282212.1:c.283G>C, NM_001282212.1:c.283G>A, NM_001282214.2:c.283G>C, NM_001282214.2:c.283G>A, NM_001282214.1:c.283G>C, NM_001282214.1:c.283G>A, NM_001354561.2:c.283G>C, NM_001354561.2:c.283G>A, NM_001354561.1:c.283G>C, NM_001354561.1:c.283G>A, NM_001282213.2:c.283G>C, NM_001282213.2:c.283G>A, NM_001282213.1:c.283G>C, NM_001282213.1:c.283G>A, NM_001354559.2:c.325G>C, NM_001354559.2:c.325G>A, NM_001354559.1:c.325G>C, NM_001354559.1:c.325G>A, NM_201535.2:c.325G>C, NM_201535.2:c.325G>A, NM_201535.1:c.325G>C, NM_201535.1:c.325G>A, NM_001354562.2:c.325G>C, NM_001354562.2:c.325G>A, NM_001354562.1:c.325G>C, NM_001354562.1:c.325G>A, NM_201540.2:c.325G>C, NM_201540.2:c.325G>A, NM_201540.1:c.325G>C, NM_201540.1:c.325G>A, NM_001354558.2:c.325G>C, NM_001354558.2:c.325G>A, NM_001354558.1:c.325G>C, NM_001354558.1:c.325G>A, NM_201537.2:c.325G>C, NM_201537.2:c.325G>A, NM_201537.1:c.325G>C, NM_201537.1:c.325G>A, NM_201541.2:c.283G>C, NM_201541.2:c.283G>A, NM_201541.1:c.283G>C, NM_201541.1:c.283G>A, NM_001282215.2:c.325G>C, NM_001282215.2:c.325G>A, NM_001282215.1:c.325G>C, NM_001282215.1:c.325G>A, NM_201536.2:c.283G>C, NM_201536.2:c.283G>A, NM_201536.1:c.283G>C, NM_201536.1:c.283G>A, NM_201539.2:c.325G>C, NM_201539.2:c.325G>A, NM_201539.1:c.325G>C, NM_201539.1:c.325G>A, NM_001354564.2:c.325G>C, NM_001354564.2:c.325G>A, NM_001354564.1:c.325G>C, NM_001354564.1:c.325G>A, NM_001282211.2:c.313G>C, NM_001282211.2:c.313G>A, NM_001282211.1:c.313G>C, NM_001282211.1:c.313G>A, NM_201538.2:c.283G>C, NM_201538.2:c.283G>A, NM_201538.1:c.283G>C, NM_201538.1:c.283G>A, NM_001282216.2:c.145G>C, NM_001282216.2:c.145G>A, NM_001282216.1:c.145G>C, NM_001282216.1:c.145G>A, NM_001354560.2:c.283G>C, NM_001354560.2:c.283G>A, NM_001354560.1:c.283G>C, NM_001354560.1:c.283G>A, NM_001354569.1:c.283G>C, NM_001354569.1:c.283G>A, NM_001354566.1:c.325G>C, NM_001354566.1:c.325G>A, NP_057334.1:p.Ala95Pro, NP_057334.1:p.Ala95Thr, NP_001307258.1:p.Ala109Pro, NP_001307258.1:p.Ala109Thr, NP_001341494.1:p.Ala109Pro, NP_001341494.1:p.Ala109Thr, NP_001341497.1:p.Ala95Pro, NP_001341497.1:p.Ala95Thr, NP_001341499.1:p.Ala109Pro, NP_001341499.1:p.Ala109Thr, NP_001341496.1:p.Ala109Pro, NP_001341496.1:p.Ala109Thr, NP_001269141.1:p.Ala95Pro, NP_001269141.1:p.Ala95Thr, NP_001269143.1:p.Ala95Pro, NP_001269143.1:p.Ala95Thr, NP_001341490.1:p.Ala95Pro, NP_001341490.1:p.Ala95Thr, NP_001269142.1:p.Ala95Pro, NP_001269142.1:p.Ala95Thr, NP_001341488.1:p.Ala109Pro, NP_001341488.1:p.Ala109Thr, NP_963293.1:p.Ala109Pro, NP_963293.1:p.Ala109Thr, NP_001341491.1:p.Ala109Pro, NP_001341491.1:p.Ala109Thr, NP_963834.1:p.Ala109Pro, NP_963834.1:p.Ala109Thr, NP_001341487.1:p.Ala109Pro, NP_001341487.1:p.Ala109Thr, NP_963831.1:p.Ala109Pro, NP_963831.1:p.Ala109Thr, NP_963835.1:p.Ala95Pro, NP_963835.1:p.Ala95Thr, NP_001269144.1:p.Ala109Pro, NP_001269144.1:p.Ala109Thr, NP_963294.1:p.Ala95Pro, NP_963294.1:p.Ala95Thr, NP_963833.1:p.Ala109Pro, NP_963833.1:p.Ala109Thr, NP_001341493.1:p.Ala109Pro, NP_001341493.1:p.Ala109Thr, NP_001269140.1:p.Ala105Pro, NP_001269140.1:p.Ala105Thr, NP_963832.1:p.Ala95Pro, NP_963832.1:p.Ala95Thr, NP_001269145.1:p.Ala49Pro, NP_001269145.1:p.Ala49Thr, NP_001341489.1:p.Ala95Pro, NP_001341489.1:p.Ala95Thr, NP_001341498.1:p.Ala95Pro, NP_001341498.1:p.Ala95Thr, NP_001341495.1:p.Ala109Pro, NP_001341495.1:p.Ala109Thr

                                        20.

                                        rs1436902099 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          C>A [Show Flanks]
                                          Chromosome:
                                          14:21019131 (GRCh38)
                                          14:21487290 (GRCh37)
                                          Canonical SPDI:
                                          NC_000014.9:21019130:C:A
                                          Gene:
                                          NDRG2 (Varview)
                                          Functional Consequence:
                                          coding_sequence_variant,missense_variant
                                          Validated:
                                          by frequency,by alfa
                                          MAF:
                                          A=0./0 (ALFA)
                                          A=0.000011/3 (TOPMED)
                                          HGVS:
                                          NC_000014.9:g.21019131C>A, NC_000014.8:g.21487290C>A, NM_016250.3:c.704G>T, NM_016250.2:c.704G>T, NM_001320329.2:c.746G>T, NM_001320329.1:c.746G>T, NM_001354565.2:c.746G>T, NM_001354565.1:c.746G>T, NM_001354568.2:c.704G>T, NM_001354568.1:c.704G>T, NM_001354570.2:c.746G>T, NM_001354570.1:c.746G>T, NM_001354567.2:c.746G>T, NM_001354567.1:c.746G>T, NM_001282212.2:c.704G>T, NM_001282212.1:c.704G>T, NM_001282214.2:c.704G>T, NM_001282214.1:c.704G>T, NM_001354561.2:c.704G>T, NM_001354561.1:c.704G>T, NM_001282213.2:c.704G>T, NM_001282213.1:c.704G>T, NM_001354559.2:c.746G>T, NM_001354559.1:c.746G>T, NM_201535.2:c.746G>T, NM_201535.1:c.746G>T, NM_001354562.2:c.746G>T, NM_001354562.1:c.746G>T, NM_201540.2:c.746G>T, NM_201540.1:c.746G>T, NM_001354558.2:c.746G>T, NM_001354558.1:c.746G>T, NM_201537.2:c.746G>T, NM_201537.1:c.746G>T, NM_201541.2:c.704G>T, NM_201541.1:c.704G>T, NM_001282215.2:c.746G>T, NM_001282215.1:c.746G>T, NM_201536.2:c.704G>T, NM_201536.1:c.704G>T, NM_201539.2:c.746G>T, NM_201539.1:c.746G>T, NM_001354564.2:c.746G>T, NM_001354564.1:c.746G>T, NM_001282211.2:c.734G>T, NM_001282211.1:c.734G>T, NM_201538.2:c.704G>T, NM_201538.1:c.704G>T, NM_001282216.2:c.566G>T, NM_001282216.1:c.566G>T, NM_001354560.2:c.704G>T, NM_001354560.1:c.704G>T, NM_001354569.1:c.704G>T, NM_001354566.1:c.746G>T, NP_057334.1:p.Gly235Val, NP_001307258.1:p.Gly249Val, NP_001341494.1:p.Gly249Val, NP_001341497.1:p.Gly235Val, NP_001341499.1:p.Gly249Val, NP_001341496.1:p.Gly249Val, NP_001269141.1:p.Gly235Val, NP_001269143.1:p.Gly235Val, NP_001341490.1:p.Gly235Val, NP_001269142.1:p.Gly235Val, NP_001341488.1:p.Gly249Val, NP_963293.1:p.Gly249Val, NP_001341491.1:p.Gly249Val, NP_963834.1:p.Gly249Val, NP_001341487.1:p.Gly249Val, NP_963831.1:p.Gly249Val, NP_963835.1:p.Gly235Val, NP_001269144.1:p.Gly249Val, NP_963294.1:p.Gly235Val, NP_963833.1:p.Gly249Val, NP_001341493.1:p.Gly249Val, NP_001269140.1:p.Gly245Val, NP_963832.1:p.Gly235Val, NP_001269145.1:p.Gly189Val, NP_001341489.1:p.Gly235Val, NP_001341498.1:p.Gly235Val, NP_001341495.1:p.Gly249Val

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