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Items: 1 to 20 of 393

1.

rs1490613968 [Homo sapiens]
    Variant type:
    INS
    Alleles:
    ->T [Show Flanks]
    Chromosome:
    9:96539128 (GRCh38)
    9:99301411 (GRCh37)
    Canonical SPDI:
    NC_000009.12:96539128::T
    Gene:
    CDC14B (Varview)
    Functional Consequence:
    intron_variant,non_coding_transcript_variant,coding_sequence_variant,genic_upstream_transcript_variant,frameshift_variant
    HGVS:
    NC_000009.12:g.96539128_96539129insT, NC_000009.11:g.99301410_99301411insT, NM_003671.5:c.576_577insA, NM_003671.4:c.576_577insA, NM_003671.3:c.576_577insA, XM_011519156.4:c.558_559insA, XM_011519156.3:c.558_559insA, XM_011519156.2:c.558_559insA, XM_011519156.1:c.558_559insA, NM_033331.4:c.576_577insA, NM_033331.3:c.576_577insA, NM_033331.2:c.576_577insA, XM_011519148.4:c.507_508insA, XM_011519148.3:c.507_508insA, XM_011519148.2:c.855_856insA, XM_011519148.1:c.855_856insA, XM_011519153.4:c.507_508insA, XM_011519153.3:c.507_508insA, XM_011519153.2:c.855_856insA, XM_011519153.1:c.855_856insA, XR_929864.4:n.654_655insA, XR_929864.3:n.509_510insA, XR_929864.2:n.975_976insA, XR_929864.1:n.870_871insA, XM_011519147.4:c.507_508insA, XM_011519147.3:c.507_508insA, XM_011519147.2:c.855_856insA, XM_011519147.1:c.855_856insA, XR_929865.4:n.654_655insA, XR_929865.3:n.509_510insA, XR_929865.2:n.975_976insA, XR_929865.1:n.870_871insA, XM_011519151.4:c.507_508insA, XM_011519151.3:c.507_508insA, XM_011519151.2:c.855_856insA, XM_011519151.1:c.855_856insA, XM_011519149.4:c.507_508insA, XM_011519149.3:c.507_508insA, XM_011519149.2:c.855_856insA, XM_011519149.1:c.855_856insA, XM_017015242.3:c.576_577insA, XM_017015242.2:c.576_577insA, XM_017015242.1:c.576_577insA, XM_017015240.3:c.507_508insA, XM_017015240.2:c.507_508insA, XM_017015240.1:c.855_856insA, XM_017015244.3:c.465_466insA, XM_017015244.2:c.465_466insA, XM_017015244.1:c.465_466insA, XM_017015247.3:c.465_466insA, XM_017015247.2:c.465_466insA, XM_017015247.1:c.465_466insA, NM_001077181.3:c.465_466insA, NM_001077181.2:c.465_466insA, NM_001077181.1:c.465_466insA, NM_001351567.3:c.576_577insA, NM_001351567.2:c.576_577insA, NM_001351567.1:c.576_577insA, NM_001351568.3:c.465_466insA, NM_001351568.2:c.465_466insA, NM_001351568.1:c.465_466insA, XR_001746406.3:n.654_655insA, XR_001746406.2:n.509_510insA, XR_001746406.1:n.972_973insA, NR_147239.2:n.1041_1042insA, NR_147239.1:n.1028_1029insA, NM_001351569.2:c.465_466insA, NM_001351569.1:c.465_466insA, XM_017015245.2:c.558_559insA, XM_017015245.1:c.558_559insA, XM_047424001.1:c.291_292insA, XM_047424003.1:c.291_292insA, XM_047424002.1:c.291_292insA, XM_047424004.1:c.291_292insA, NM_001351570.1:c.507_508insA, NM_033332.1:c.576_577insA, XM_047424005.1:c.9_10insA, XR_007061367.1:n.654_655insA, XR_007061366.1:n.654_655insA, XM_047423999.1:c.576_577insA, XM_047423998.1:c.576_577insA, XM_047423997.1:c.507_508insA, NP_003662.1:p.Gly193fs, XP_011517458.2:p.Gly187fs, NP_201588.1:p.Gly193fs, XP_011517450.2:p.Gly170fs, XP_011517455.2:p.Gly170fs, XP_011517449.2:p.Gly170fs, XP_011517453.2:p.Gly170fs, XP_011517451.2:p.Gly170fs, XP_016870731.1:p.Gly193fs, XP_016870729.2:p.Gly170fs, XP_016870733.1:p.Gly156fs, XP_016870736.1:p.Gly156fs, NP_001070649.1:p.Gly156fs, NP_001338496.1:p.Gly193fs, NP_001338497.1:p.Gly156fs, NP_001338498.1:p.Gly156fs, XP_016870734.1:p.Gly187fs, XP_047279957.1:p.Gly98fs, XP_047279959.1:p.Gly98fs, XP_047279958.1:p.Gly98fs, XP_047279960.1:p.Gly98fs, NP_001338499.1:p.Gly170fs, XP_047279961.1:p.Gly4fs, XP_047279955.1:p.Gly193fs, XP_047279954.1:p.Gly193fs, XP_047279953.1:p.Gly170fs

    2.

    rs1489805735 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      A>G [Show Flanks]
      Chromosome:
      9:96523683 (GRCh38)
      9:99285965 (GRCh37)
      Canonical SPDI:
      NC_000009.12:96523682:A:G
      Gene:
      CDC14B (Varview)
      Functional Consequence:
      coding_sequence_variant,non_coding_transcript_variant,missense_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      G=0./0 (ALFA)
      G=0.000004/1 (TOPMED)
      G=0.000007/1 (GnomAD)
      G=0.000008/2 (GnomAD_exomes)
      HGVS:
      NC_000009.12:g.96523683A>G, NC_000009.11:g.99285965A>G, NM_003671.5:c.989T>C, NM_003671.4:c.989T>C, NM_003671.3:c.989T>C, XM_011519156.4:c.971T>C, XM_011519156.3:c.971T>C, XM_011519156.2:c.971T>C, XM_011519156.1:c.971T>C, NM_033331.4:c.989T>C, NM_033331.3:c.989T>C, NM_033331.2:c.989T>C, XM_011519148.4:c.920T>C, XM_011519148.3:c.920T>C, XM_011519148.2:c.1268T>C, XM_011519148.1:c.1268T>C, XM_011519153.4:c.920T>C, XM_011519153.3:c.920T>C, XM_011519153.2:c.1268T>C, XM_011519153.1:c.1268T>C, XR_929864.4:n.1067T>C, XR_929864.3:n.922T>C, XR_929864.2:n.1388T>C, XR_929864.1:n.1283T>C, XM_011519147.4:c.920T>C, XM_011519147.3:c.920T>C, XM_011519147.2:c.1268T>C, XM_011519147.1:c.1268T>C, XR_929865.4:n.1067T>C, XR_929865.3:n.922T>C, XR_929865.2:n.1388T>C, XR_929865.1:n.1283T>C, XM_011519151.4:c.920T>C, XM_011519151.3:c.920T>C, XM_011519151.2:c.1268T>C, XM_011519151.1:c.1268T>C, XM_011519149.4:c.920T>C, XM_011519149.3:c.920T>C, XM_011519149.2:c.1268T>C, XM_011519149.1:c.1268T>C, XM_017015242.3:c.989T>C, XM_017015242.2:c.989T>C, XM_017015242.1:c.989T>C, XM_017015240.3:c.920T>C, XM_017015240.2:c.920T>C, XM_017015240.1:c.1268T>C, XM_017015248.3:c.782T>C, XM_017015248.2:c.782T>C, XM_017015248.1:c.782T>C, XM_017015244.3:c.878T>C, XM_017015244.2:c.878T>C, XM_017015244.1:c.878T>C, XM_017015241.3:c.713T>C, XM_017015241.2:c.713T>C, XM_017015241.1:c.1061T>C, XM_017015247.3:c.878T>C, XM_017015247.2:c.878T>C, XM_017015247.1:c.878T>C, NM_001077181.3:c.878T>C, NM_001077181.2:c.878T>C, NM_001077181.1:c.878T>C, NM_001351567.3:c.989T>C, NM_001351567.2:c.989T>C, NM_001351567.1:c.989T>C, NM_001351568.3:c.878T>C, NM_001351568.2:c.878T>C, NM_001351568.1:c.878T>C, XR_001746406.3:n.1067T>C, XR_001746406.2:n.922T>C, XR_001746406.1:n.1385T>C, NR_147239.2:n.1454T>C, NR_147239.1:n.1441T>C, NM_001351569.2:c.878T>C, NM_001351569.1:c.878T>C, XM_017015245.2:c.971T>C, XM_017015245.1:c.971T>C, XM_047424001.1:c.704T>C, XM_047424003.1:c.704T>C, XM_047424002.1:c.704T>C, XM_047424004.1:c.704T>C, XM_047424000.1:c.782T>C, NM_001351570.1:c.920T>C, NM_033332.1:c.989T>C, XM_047424005.1:c.422T>C, XM_047424006.1:c.191T>C, XR_007061367.1:n.1067T>C, XR_007061366.1:n.1067T>C, XM_047423999.1:c.989T>C, XM_047423998.1:c.989T>C, XM_047423997.1:c.920T>C, NP_003662.1:p.Met330Thr, XP_011517458.2:p.Met324Thr, NP_201588.1:p.Met330Thr, XP_011517450.2:p.Met307Thr, XP_011517455.2:p.Met307Thr, XP_011517449.2:p.Met307Thr, XP_011517453.2:p.Met307Thr, XP_011517451.2:p.Met307Thr, XP_016870731.1:p.Met330Thr, XP_016870729.2:p.Met307Thr, XP_016870737.1:p.Met261Thr, XP_016870733.1:p.Met293Thr, XP_016870730.2:p.Met238Thr, XP_016870736.1:p.Met293Thr, NP_001070649.1:p.Met293Thr, NP_001338496.1:p.Met330Thr, NP_001338497.1:p.Met293Thr, NP_001338498.1:p.Met293Thr, XP_016870734.1:p.Met324Thr, XP_047279957.1:p.Met235Thr, XP_047279959.1:p.Met235Thr, XP_047279958.1:p.Met235Thr, XP_047279960.1:p.Met235Thr, XP_047279956.1:p.Met261Thr, NP_001338499.1:p.Met307Thr, XP_047279961.1:p.Met141Thr, XP_047279962.1:p.Met64Thr, XP_047279955.1:p.Met330Thr, XP_047279954.1:p.Met330Thr, XP_047279953.1:p.Met307Thr

      3.

      rs1489178024 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        T>C [Show Flanks]
        Chromosome:
        9:96523409 (GRCh38)
        9:99285691 (GRCh37)
        Canonical SPDI:
        NC_000009.12:96523408:T:C
        Gene:
        CDC14B (Varview)
        Functional Consequence:
        coding_sequence_variant,non_coding_transcript_variant,missense_variant
        Validated:
        by frequency,by alfa
        MAF:
        C=0./0 (ALFA)
        HGVS:
        NC_000009.12:g.96523409T>C, NC_000009.11:g.99285691T>C, NM_003671.5:c.1097A>G, NM_003671.4:c.1097A>G, NM_003671.3:c.1097A>G, XM_011519156.4:c.1079A>G, XM_011519156.3:c.1079A>G, XM_011519156.2:c.1079A>G, XM_011519156.1:c.1079A>G, NM_033331.4:c.1097A>G, NM_033331.3:c.1097A>G, NM_033331.2:c.1097A>G, XM_011519148.4:c.1028A>G, XM_011519148.3:c.1028A>G, XM_011519148.2:c.1376A>G, XM_011519148.1:c.1376A>G, XM_011519153.4:c.1028A>G, XM_011519153.3:c.1028A>G, XM_011519153.2:c.1376A>G, XM_011519153.1:c.1376A>G, XR_929864.4:n.1175A>G, XR_929864.3:n.1030A>G, XR_929864.2:n.1496A>G, XR_929864.1:n.1391A>G, XM_011519147.4:c.1028A>G, XM_011519147.3:c.1028A>G, XM_011519147.2:c.1376A>G, XM_011519147.1:c.1376A>G, XR_929865.4:n.1175A>G, XR_929865.3:n.1030A>G, XR_929865.2:n.1496A>G, XR_929865.1:n.1391A>G, XM_011519151.4:c.1028A>G, XM_011519151.3:c.1028A>G, XM_011519151.2:c.1376A>G, XM_011519151.1:c.1376A>G, XM_011519149.4:c.1028A>G, XM_011519149.3:c.1028A>G, XM_011519149.2:c.1376A>G, XM_011519149.1:c.1376A>G, XM_017015242.3:c.1097A>G, XM_017015242.2:c.1097A>G, XM_017015242.1:c.1097A>G, XM_017015240.3:c.1028A>G, XM_017015240.2:c.1028A>G, XM_017015240.1:c.1376A>G, XM_017015248.3:c.890A>G, XM_017015248.2:c.890A>G, XM_017015248.1:c.890A>G, XM_017015244.3:c.986A>G, XM_017015244.2:c.986A>G, XM_017015244.1:c.986A>G, XM_017015241.3:c.821A>G, XM_017015241.2:c.821A>G, XM_017015241.1:c.1169A>G, XM_017015247.3:c.986A>G, XM_017015247.2:c.986A>G, XM_017015247.1:c.986A>G, NM_001077181.3:c.986A>G, NM_001077181.2:c.986A>G, NM_001077181.1:c.986A>G, NM_001351567.3:c.1097A>G, NM_001351567.2:c.1097A>G, NM_001351567.1:c.1097A>G, NM_001351568.3:c.986A>G, NM_001351568.2:c.986A>G, NM_001351568.1:c.986A>G, XR_001746406.3:n.1175A>G, XR_001746406.2:n.1030A>G, XR_001746406.1:n.1493A>G, NR_147239.2:n.1562A>G, NR_147239.1:n.1549A>G, NM_001351569.2:c.986A>G, NM_001351569.1:c.986A>G, XM_017015245.2:c.1079A>G, XM_017015245.1:c.1079A>G, XM_047424001.1:c.812A>G, XM_047424003.1:c.812A>G, XM_047424002.1:c.812A>G, XM_047424004.1:c.812A>G, XM_047424000.1:c.890A>G, NM_001351570.1:c.1028A>G, NM_033332.1:c.1097A>G, XM_047424005.1:c.530A>G, XM_047424006.1:c.299A>G, XR_007061367.1:n.1175A>G, XR_007061366.1:n.1175A>G, XM_047423999.1:c.1097A>G, XM_047423998.1:c.1097A>G, XM_047423997.1:c.1028A>G, NP_003662.1:p.Asn366Ser, XP_011517458.2:p.Asn360Ser, NP_201588.1:p.Asn366Ser, XP_011517450.2:p.Asn343Ser, XP_011517455.2:p.Asn343Ser, XP_011517449.2:p.Asn343Ser, XP_011517453.2:p.Asn343Ser, XP_011517451.2:p.Asn343Ser, XP_016870731.1:p.Asn366Ser, XP_016870729.2:p.Asn343Ser, XP_016870737.1:p.Asn297Ser, XP_016870733.1:p.Asn329Ser, XP_016870730.2:p.Asn274Ser, XP_016870736.1:p.Asn329Ser, NP_001070649.1:p.Asn329Ser, NP_001338496.1:p.Asn366Ser, NP_001338497.1:p.Asn329Ser, NP_001338498.1:p.Asn329Ser, XP_016870734.1:p.Asn360Ser, XP_047279957.1:p.Asn271Ser, XP_047279959.1:p.Asn271Ser, XP_047279958.1:p.Asn271Ser, XP_047279960.1:p.Asn271Ser, XP_047279956.1:p.Asn297Ser, NP_001338499.1:p.Asn343Ser, XP_047279961.1:p.Asn177Ser, XP_047279962.1:p.Asn100Ser, XP_047279955.1:p.Asn366Ser, XP_047279954.1:p.Asn366Ser, XP_047279953.1:p.Asn343Ser

        4.

        rs1484221385 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          C>T [Show Flanks]
          Chromosome:
          9:96562725 (GRCh38)
          9:99325007 (GRCh37)
          Canonical SPDI:
          NC_000009.12:96562724:C:T
          Gene:
          CDC14B (Varview)
          Functional Consequence:
          missense_variant,5_prime_UTR_variant,non_coding_transcript_variant,coding_sequence_variant,genic_upstream_transcript_variant
          Validated:
          by frequency
          MAF:
          T=0.000004/1 (GnomAD_exomes)
          HGVS:
          NC_000009.12:g.96562725C>T, NC_000009.11:g.99325007C>T, NM_003671.5:c.388G>A, NM_003671.4:c.388G>A, NM_003671.3:c.388G>A, XM_011519156.4:c.370G>A, XM_011519156.3:c.370G>A, XM_011519156.2:c.370G>A, XM_011519156.1:c.370G>A, NM_033331.4:c.388G>A, NM_033331.3:c.388G>A, NM_033331.2:c.388G>A, XM_011519148.4:c.319G>A, XM_011519148.3:c.319G>A, XM_011519148.2:c.667G>A, XM_011519148.1:c.667G>A, XM_011519153.4:c.319G>A, XM_011519153.3:c.319G>A, XM_011519153.2:c.667G>A, XM_011519153.1:c.667G>A, XR_929864.4:n.466G>A, XR_929864.3:n.321G>A, XR_929864.2:n.787G>A, XR_929864.1:n.682G>A, XM_011519147.4:c.319G>A, XM_011519147.3:c.319G>A, XM_011519147.2:c.667G>A, XM_011519147.1:c.667G>A, XR_929865.4:n.466G>A, XR_929865.3:n.321G>A, XR_929865.2:n.787G>A, XR_929865.1:n.682G>A, XM_011519151.4:c.319G>A, XM_011519151.3:c.319G>A, XM_011519151.2:c.667G>A, XM_011519151.1:c.667G>A, XM_011519149.4:c.319G>A, XM_011519149.3:c.319G>A, XM_011519149.2:c.667G>A, XM_011519149.1:c.667G>A, XM_017015242.3:c.388G>A, XM_017015242.2:c.388G>A, XM_017015242.1:c.388G>A, XM_017015240.3:c.319G>A, XM_017015240.2:c.319G>A, XM_017015240.1:c.667G>A, XM_017015248.3:c.388G>A, XM_017015248.2:c.388G>A, XM_017015248.1:c.388G>A, XM_017015244.3:c.277G>A, XM_017015244.2:c.277G>A, XM_017015244.1:c.277G>A, XM_017015241.3:c.319G>A, XM_017015241.2:c.319G>A, XM_017015241.1:c.667G>A, XM_017015247.3:c.277G>A, XM_017015247.2:c.277G>A, XM_017015247.1:c.277G>A, NM_001077181.3:c.277G>A, NM_001077181.2:c.277G>A, NM_001077181.1:c.277G>A, NM_001351567.3:c.388G>A, NM_001351567.2:c.388G>A, NM_001351567.1:c.388G>A, NM_001351568.3:c.277G>A, NM_001351568.2:c.277G>A, NM_001351568.1:c.277G>A, XR_001746406.3:n.466G>A, XR_001746406.2:n.321G>A, XR_001746406.1:n.784G>A, NR_147239.2:n.853G>A, NR_147239.1:n.840G>A, NM_001351569.2:c.277G>A, NM_001351569.1:c.277G>A, XM_017015245.2:c.370G>A, XM_017015245.1:c.370G>A, XM_047424001.1:c.103G>A, XM_047424003.1:c.103G>A, XM_047424002.1:c.103G>A, XM_047424004.1:c.103G>A, XM_047424000.1:c.388G>A, NM_001351570.1:c.319G>A, NM_033332.1:c.388G>A, XM_047424005.1:c.-103G>A, XR_007061367.1:n.466G>A, XR_007061366.1:n.466G>A, XM_047423999.1:c.388G>A, XM_047423998.1:c.388G>A, XM_047423997.1:c.319G>A, NP_003662.1:p.Ala130Thr, XP_011517458.2:p.Ala124Thr, NP_201588.1:p.Ala130Thr, XP_011517450.2:p.Ala107Thr, XP_011517455.2:p.Ala107Thr, XP_011517449.2:p.Ala107Thr, XP_011517453.2:p.Ala107Thr, XP_011517451.2:p.Ala107Thr, XP_016870731.1:p.Ala130Thr, XP_016870729.2:p.Ala107Thr, XP_016870737.1:p.Ala130Thr, XP_016870733.1:p.Ala93Thr, XP_016870730.2:p.Ala107Thr, XP_016870736.1:p.Ala93Thr, NP_001070649.1:p.Ala93Thr, NP_001338496.1:p.Ala130Thr, NP_001338497.1:p.Ala93Thr, NP_001338498.1:p.Ala93Thr, XP_016870734.1:p.Ala124Thr, XP_047279957.1:p.Ala35Thr, XP_047279959.1:p.Ala35Thr, XP_047279958.1:p.Ala35Thr, XP_047279960.1:p.Ala35Thr, XP_047279956.1:p.Ala130Thr, NP_001338499.1:p.Ala107Thr, XP_047279955.1:p.Ala130Thr, XP_047279954.1:p.Ala130Thr, XP_047279953.1:p.Ala107Thr

          5.

          rs1482593867 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            A>C [Show Flanks]
            Chromosome:
            9:96523596 (GRCh38)
            9:99285878 (GRCh37)
            Canonical SPDI:
            NC_000009.12:96523595:A:C
            Gene:
            CDC14B (Varview)
            Functional Consequence:
            coding_sequence_variant,non_coding_transcript_variant,missense_variant
            Validated:
            by frequency
            MAF:
            C=0.000004/1 (GnomAD_exomes)
            HGVS:
            NC_000009.12:g.96523596A>C, NC_000009.11:g.99285878A>C, NM_003671.5:c.1076T>G, NM_003671.4:c.1076T>G, NM_003671.3:c.1076T>G, XM_011519156.4:c.1058T>G, XM_011519156.3:c.1058T>G, XM_011519156.2:c.1058T>G, XM_011519156.1:c.1058T>G, NM_033331.4:c.1076T>G, NM_033331.3:c.1076T>G, NM_033331.2:c.1076T>G, XM_011519148.4:c.1007T>G, XM_011519148.3:c.1007T>G, XM_011519148.2:c.1355T>G, XM_011519148.1:c.1355T>G, XM_011519153.4:c.1007T>G, XM_011519153.3:c.1007T>G, XM_011519153.2:c.1355T>G, XM_011519153.1:c.1355T>G, XR_929864.4:n.1154T>G, XR_929864.3:n.1009T>G, XR_929864.2:n.1475T>G, XR_929864.1:n.1370T>G, XM_011519147.4:c.1007T>G, XM_011519147.3:c.1007T>G, XM_011519147.2:c.1355T>G, XM_011519147.1:c.1355T>G, XR_929865.4:n.1154T>G, XR_929865.3:n.1009T>G, XR_929865.2:n.1475T>G, XR_929865.1:n.1370T>G, XM_011519151.4:c.1007T>G, XM_011519151.3:c.1007T>G, XM_011519151.2:c.1355T>G, XM_011519151.1:c.1355T>G, XM_011519149.4:c.1007T>G, XM_011519149.3:c.1007T>G, XM_011519149.2:c.1355T>G, XM_011519149.1:c.1355T>G, XM_017015242.3:c.1076T>G, XM_017015242.2:c.1076T>G, XM_017015242.1:c.1076T>G, XM_017015240.3:c.1007T>G, XM_017015240.2:c.1007T>G, XM_017015240.1:c.1355T>G, XM_017015248.3:c.869T>G, XM_017015248.2:c.869T>G, XM_017015248.1:c.869T>G, XM_017015244.3:c.965T>G, XM_017015244.2:c.965T>G, XM_017015244.1:c.965T>G, XM_017015241.3:c.800T>G, XM_017015241.2:c.800T>G, XM_017015241.1:c.1148T>G, XM_017015247.3:c.965T>G, XM_017015247.2:c.965T>G, XM_017015247.1:c.965T>G, NM_001077181.3:c.965T>G, NM_001077181.2:c.965T>G, NM_001077181.1:c.965T>G, NM_001351567.3:c.1076T>G, NM_001351567.2:c.1076T>G, NM_001351567.1:c.1076T>G, NM_001351568.3:c.965T>G, NM_001351568.2:c.965T>G, NM_001351568.1:c.965T>G, XR_001746406.3:n.1154T>G, XR_001746406.2:n.1009T>G, XR_001746406.1:n.1472T>G, NR_147239.2:n.1541T>G, NR_147239.1:n.1528T>G, NM_001351569.2:c.965T>G, NM_001351569.1:c.965T>G, XM_017015245.2:c.1058T>G, XM_017015245.1:c.1058T>G, XM_047424001.1:c.791T>G, XM_047424003.1:c.791T>G, XM_047424002.1:c.791T>G, XM_047424004.1:c.791T>G, XM_047424000.1:c.869T>G, NM_001351570.1:c.1007T>G, NM_033332.1:c.1076T>G, XM_047424005.1:c.509T>G, XM_047424006.1:c.278T>G, XR_007061367.1:n.1154T>G, XR_007061366.1:n.1154T>G, XM_047423999.1:c.1076T>G, XM_047423998.1:c.1076T>G, XM_047423997.1:c.1007T>G, NP_003662.1:p.Phe359Cys, XP_011517458.2:p.Phe353Cys, NP_201588.1:p.Phe359Cys, XP_011517450.2:p.Phe336Cys, XP_011517455.2:p.Phe336Cys, XP_011517449.2:p.Phe336Cys, XP_011517453.2:p.Phe336Cys, XP_011517451.2:p.Phe336Cys, XP_016870731.1:p.Phe359Cys, XP_016870729.2:p.Phe336Cys, XP_016870737.1:p.Phe290Cys, XP_016870733.1:p.Phe322Cys, XP_016870730.2:p.Phe267Cys, XP_016870736.1:p.Phe322Cys, NP_001070649.1:p.Phe322Cys, NP_001338496.1:p.Phe359Cys, NP_001338497.1:p.Phe322Cys, NP_001338498.1:p.Phe322Cys, XP_016870734.1:p.Phe353Cys, XP_047279957.1:p.Phe264Cys, XP_047279959.1:p.Phe264Cys, XP_047279958.1:p.Phe264Cys, XP_047279960.1:p.Phe264Cys, XP_047279956.1:p.Phe290Cys, NP_001338499.1:p.Phe336Cys, XP_047279961.1:p.Phe170Cys, XP_047279962.1:p.Phe93Cys, XP_047279955.1:p.Phe359Cys, XP_047279954.1:p.Phe359Cys, XP_047279953.1:p.Phe336Cys

            6.

            rs1481012021 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              A>T [Show Flanks]
              Chromosome:
              9:96523587 (GRCh38)
              9:99285869 (GRCh37)
              Canonical SPDI:
              NC_000009.12:96523586:A:T
              Gene:
              CDC14B (Varview)
              Functional Consequence:
              coding_sequence_variant,non_coding_transcript_variant,missense_variant
              Validated:
              by frequency
              MAF:
              T=0.000004/1 (GnomAD_exomes)
              HGVS:
              NC_000009.12:g.96523587A>T, NC_000009.11:g.99285869A>T, NM_003671.5:c.1085T>A, NM_003671.4:c.1085T>A, NM_003671.3:c.1085T>A, XM_011519156.4:c.1067T>A, XM_011519156.3:c.1067T>A, XM_011519156.2:c.1067T>A, XM_011519156.1:c.1067T>A, NM_033331.4:c.1085T>A, NM_033331.3:c.1085T>A, NM_033331.2:c.1085T>A, XM_011519148.4:c.1016T>A, XM_011519148.3:c.1016T>A, XM_011519148.2:c.1364T>A, XM_011519148.1:c.1364T>A, XM_011519153.4:c.1016T>A, XM_011519153.3:c.1016T>A, XM_011519153.2:c.1364T>A, XM_011519153.1:c.1364T>A, XR_929864.4:n.1163T>A, XR_929864.3:n.1018T>A, XR_929864.2:n.1484T>A, XR_929864.1:n.1379T>A, XM_011519147.4:c.1016T>A, XM_011519147.3:c.1016T>A, XM_011519147.2:c.1364T>A, XM_011519147.1:c.1364T>A, XR_929865.4:n.1163T>A, XR_929865.3:n.1018T>A, XR_929865.2:n.1484T>A, XR_929865.1:n.1379T>A, XM_011519151.4:c.1016T>A, XM_011519151.3:c.1016T>A, XM_011519151.2:c.1364T>A, XM_011519151.1:c.1364T>A, XM_011519149.4:c.1016T>A, XM_011519149.3:c.1016T>A, XM_011519149.2:c.1364T>A, XM_011519149.1:c.1364T>A, XM_017015242.3:c.1085T>A, XM_017015242.2:c.1085T>A, XM_017015242.1:c.1085T>A, XM_017015240.3:c.1016T>A, XM_017015240.2:c.1016T>A, XM_017015240.1:c.1364T>A, XM_017015248.3:c.878T>A, XM_017015248.2:c.878T>A, XM_017015248.1:c.878T>A, XM_017015244.3:c.974T>A, XM_017015244.2:c.974T>A, XM_017015244.1:c.974T>A, XM_017015241.3:c.809T>A, XM_017015241.2:c.809T>A, XM_017015241.1:c.1157T>A, XM_017015247.3:c.974T>A, XM_017015247.2:c.974T>A, XM_017015247.1:c.974T>A, NM_001077181.3:c.974T>A, NM_001077181.2:c.974T>A, NM_001077181.1:c.974T>A, NM_001351567.3:c.1085T>A, NM_001351567.2:c.1085T>A, NM_001351567.1:c.1085T>A, NM_001351568.3:c.974T>A, NM_001351568.2:c.974T>A, NM_001351568.1:c.974T>A, XR_001746406.3:n.1163T>A, XR_001746406.2:n.1018T>A, XR_001746406.1:n.1481T>A, NR_147239.2:n.1550T>A, NR_147239.1:n.1537T>A, NM_001351569.2:c.974T>A, NM_001351569.1:c.974T>A, XM_017015245.2:c.1067T>A, XM_017015245.1:c.1067T>A, XM_047424001.1:c.800T>A, XM_047424003.1:c.800T>A, XM_047424002.1:c.800T>A, XM_047424004.1:c.800T>A, XM_047424000.1:c.878T>A, NM_001351570.1:c.1016T>A, NM_033332.1:c.1085T>A, XM_047424005.1:c.518T>A, XM_047424006.1:c.287T>A, XR_007061367.1:n.1163T>A, XR_007061366.1:n.1163T>A, XM_047423999.1:c.1085T>A, XM_047423998.1:c.1085T>A, XM_047423997.1:c.1016T>A, NP_003662.1:p.Met362Lys, XP_011517458.2:p.Met356Lys, NP_201588.1:p.Met362Lys, XP_011517450.2:p.Met339Lys, XP_011517455.2:p.Met339Lys, XP_011517449.2:p.Met339Lys, XP_011517453.2:p.Met339Lys, XP_011517451.2:p.Met339Lys, XP_016870731.1:p.Met362Lys, XP_016870729.2:p.Met339Lys, XP_016870737.1:p.Met293Lys, XP_016870733.1:p.Met325Lys, XP_016870730.2:p.Met270Lys, XP_016870736.1:p.Met325Lys, NP_001070649.1:p.Met325Lys, NP_001338496.1:p.Met362Lys, NP_001338497.1:p.Met325Lys, NP_001338498.1:p.Met325Lys, XP_016870734.1:p.Met356Lys, XP_047279957.1:p.Met267Lys, XP_047279959.1:p.Met267Lys, XP_047279958.1:p.Met267Lys, XP_047279960.1:p.Met267Lys, XP_047279956.1:p.Met293Lys, NP_001338499.1:p.Met339Lys, XP_047279961.1:p.Met173Lys, XP_047279962.1:p.Met96Lys, XP_047279955.1:p.Met362Lys, XP_047279954.1:p.Met362Lys, XP_047279953.1:p.Met339Lys

              7.

              rs1480851227 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                A>G [Show Flanks]
                Chromosome:
                9:96534091 (GRCh38)
                9:99296373 (GRCh37)
                Canonical SPDI:
                NC_000009.12:96534090:A:G
                Gene:
                CDC14B (Varview)
                Functional Consequence:
                coding_sequence_variant,non_coding_transcript_variant,missense_variant,5_prime_UTR_variant
                Validated:
                by frequency
                MAF:
                G=0.000004/1 (GnomAD_exomes)
                HGVS:
                NC_000009.12:g.96534091A>G, NC_000009.11:g.99296373A>G, NM_003671.5:c.782T>C, NM_003671.4:c.782T>C, NM_003671.3:c.782T>C, XM_011519156.4:c.764T>C, XM_011519156.3:c.764T>C, XM_011519156.2:c.764T>C, XM_011519156.1:c.764T>C, NM_033331.4:c.782T>C, NM_033331.3:c.782T>C, NM_033331.2:c.782T>C, XM_011519148.4:c.713T>C, XM_011519148.3:c.713T>C, XM_011519148.2:c.1061T>C, XM_011519148.1:c.1061T>C, XM_011519153.4:c.713T>C, XM_011519153.3:c.713T>C, XM_011519153.2:c.1061T>C, XM_011519153.1:c.1061T>C, XR_929864.4:n.860T>C, XR_929864.3:n.715T>C, XR_929864.2:n.1181T>C, XR_929864.1:n.1076T>C, XM_011519147.4:c.713T>C, XM_011519147.3:c.713T>C, XM_011519147.2:c.1061T>C, XM_011519147.1:c.1061T>C, XR_929865.4:n.860T>C, XR_929865.3:n.715T>C, XR_929865.2:n.1181T>C, XR_929865.1:n.1076T>C, XM_011519151.4:c.713T>C, XM_011519151.3:c.713T>C, XM_011519151.2:c.1061T>C, XM_011519151.1:c.1061T>C, XM_011519149.4:c.713T>C, XM_011519149.3:c.713T>C, XM_011519149.2:c.1061T>C, XM_011519149.1:c.1061T>C, XM_017015242.3:c.782T>C, XM_017015242.2:c.782T>C, XM_017015242.1:c.782T>C, XM_017015240.3:c.713T>C, XM_017015240.2:c.713T>C, XM_017015240.1:c.1061T>C, XM_017015248.3:c.575T>C, XM_017015248.2:c.575T>C, XM_017015248.1:c.575T>C, XM_017015244.3:c.671T>C, XM_017015244.2:c.671T>C, XM_017015244.1:c.671T>C, XM_017015241.3:c.506T>C, XM_017015241.2:c.506T>C, XM_017015241.1:c.854T>C, XM_017015247.3:c.671T>C, XM_017015247.2:c.671T>C, XM_017015247.1:c.671T>C, NM_001077181.3:c.671T>C, NM_001077181.2:c.671T>C, NM_001077181.1:c.671T>C, NM_001351567.3:c.782T>C, NM_001351567.2:c.782T>C, NM_001351567.1:c.782T>C, NM_001351568.3:c.671T>C, NM_001351568.2:c.671T>C, NM_001351568.1:c.671T>C, XR_001746406.3:n.860T>C, XR_001746406.2:n.715T>C, XR_001746406.1:n.1178T>C, NR_147239.2:n.1247T>C, NR_147239.1:n.1234T>C, NM_001351569.2:c.671T>C, NM_001351569.1:c.671T>C, XM_017015245.2:c.764T>C, XM_017015245.1:c.764T>C, XM_047424001.1:c.497T>C, XM_047424003.1:c.497T>C, XM_047424002.1:c.497T>C, XM_047424004.1:c.497T>C, XM_047424000.1:c.575T>C, NM_001351570.1:c.713T>C, NM_033332.1:c.782T>C, XM_047424005.1:c.215T>C, XM_047424006.1:c.-17T>C, XR_007061367.1:n.860T>C, XR_007061366.1:n.860T>C, XM_047423999.1:c.782T>C, XM_047423998.1:c.782T>C, XM_047423997.1:c.713T>C, NP_003662.1:p.Ile261Thr, XP_011517458.2:p.Ile255Thr, NP_201588.1:p.Ile261Thr, XP_011517450.2:p.Ile238Thr, XP_011517455.2:p.Ile238Thr, XP_011517449.2:p.Ile238Thr, XP_011517453.2:p.Ile238Thr, XP_011517451.2:p.Ile238Thr, XP_016870731.1:p.Ile261Thr, XP_016870729.2:p.Ile238Thr, XP_016870737.1:p.Ile192Thr, XP_016870733.1:p.Ile224Thr, XP_016870730.2:p.Ile169Thr, XP_016870736.1:p.Ile224Thr, NP_001070649.1:p.Ile224Thr, NP_001338496.1:p.Ile261Thr, NP_001338497.1:p.Ile224Thr, NP_001338498.1:p.Ile224Thr, XP_016870734.1:p.Ile255Thr, XP_047279957.1:p.Ile166Thr, XP_047279959.1:p.Ile166Thr, XP_047279958.1:p.Ile166Thr, XP_047279960.1:p.Ile166Thr, XP_047279956.1:p.Ile192Thr, NP_001338499.1:p.Ile238Thr, XP_047279961.1:p.Ile72Thr, XP_047279955.1:p.Ile261Thr, XP_047279954.1:p.Ile261Thr, XP_047279953.1:p.Ile238Thr

                8.

                rs1478401972 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  A>G,T [Show Flanks]
                  Chromosome:
                  9:96562743 (GRCh38)
                  9:99325025 (GRCh37)
                  Canonical SPDI:
                  NC_000009.12:96562742:A:G,NC_000009.12:96562742:A:T
                  Gene:
                  CDC14B (Varview)
                  Functional Consequence:
                  missense_variant,5_prime_UTR_variant,non_coding_transcript_variant,coding_sequence_variant,genic_upstream_transcript_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  G=0.000028/1 (ALFA)
                  G=0.000004/1 (GnomAD_exomes)
                  T=0.000004/1 (TOPMED)
                  T=0.000007/1 (GnomAD)
                  HGVS:
                  NC_000009.12:g.96562743A>G, NC_000009.12:g.96562743A>T, NC_000009.11:g.99325025A>G, NC_000009.11:g.99325025A>T, NM_003671.5:c.370T>C, NM_003671.5:c.370T>A, NM_003671.4:c.370T>C, NM_003671.4:c.370T>A, NM_003671.3:c.370T>C, NM_003671.3:c.370T>A, XM_011519156.4:c.352T>C, XM_011519156.4:c.352T>A, XM_011519156.3:c.352T>C, XM_011519156.3:c.352T>A, XM_011519156.2:c.352T>C, XM_011519156.2:c.352T>A, XM_011519156.1:c.352T>C, XM_011519156.1:c.352T>A, NM_033331.4:c.370T>C, NM_033331.4:c.370T>A, NM_033331.3:c.370T>C, NM_033331.3:c.370T>A, NM_033331.2:c.370T>C, NM_033331.2:c.370T>A, XM_011519148.4:c.301T>C, XM_011519148.4:c.301T>A, XM_011519148.3:c.301T>C, XM_011519148.3:c.301T>A, XM_011519148.2:c.649T>C, XM_011519148.2:c.649T>A, XM_011519148.1:c.649T>C, XM_011519148.1:c.649T>A, XM_011519153.4:c.301T>C, XM_011519153.4:c.301T>A, XM_011519153.3:c.301T>C, XM_011519153.3:c.301T>A, XM_011519153.2:c.649T>C, XM_011519153.2:c.649T>A, XM_011519153.1:c.649T>C, XM_011519153.1:c.649T>A, XR_929864.4:n.448T>C, XR_929864.4:n.448T>A, XR_929864.3:n.303T>C, XR_929864.3:n.303T>A, XR_929864.2:n.769T>C, XR_929864.2:n.769T>A, XR_929864.1:n.664T>C, XR_929864.1:n.664T>A, XM_011519147.4:c.301T>C, XM_011519147.4:c.301T>A, XM_011519147.3:c.301T>C, XM_011519147.3:c.301T>A, XM_011519147.2:c.649T>C, XM_011519147.2:c.649T>A, XM_011519147.1:c.649T>C, XM_011519147.1:c.649T>A, XR_929865.4:n.448T>C, XR_929865.4:n.448T>A, XR_929865.3:n.303T>C, XR_929865.3:n.303T>A, XR_929865.2:n.769T>C, XR_929865.2:n.769T>A, XR_929865.1:n.664T>C, XR_929865.1:n.664T>A, XM_011519151.4:c.301T>C, XM_011519151.4:c.301T>A, XM_011519151.3:c.301T>C, XM_011519151.3:c.301T>A, XM_011519151.2:c.649T>C, XM_011519151.2:c.649T>A, XM_011519151.1:c.649T>C, XM_011519151.1:c.649T>A, XM_011519149.4:c.301T>C, XM_011519149.4:c.301T>A, XM_011519149.3:c.301T>C, XM_011519149.3:c.301T>A, XM_011519149.2:c.649T>C, XM_011519149.2:c.649T>A, XM_011519149.1:c.649T>C, XM_011519149.1:c.649T>A, XM_017015242.3:c.370T>C, XM_017015242.3:c.370T>A, XM_017015242.2:c.370T>C, XM_017015242.2:c.370T>A, XM_017015242.1:c.370T>C, XM_017015242.1:c.370T>A, XM_017015240.3:c.301T>C, XM_017015240.3:c.301T>A, XM_017015240.2:c.301T>C, XM_017015240.2:c.301T>A, XM_017015240.1:c.649T>C, XM_017015240.1:c.649T>A, XM_017015248.3:c.370T>C, XM_017015248.3:c.370T>A, XM_017015248.2:c.370T>C, XM_017015248.2:c.370T>A, XM_017015248.1:c.370T>C, XM_017015248.1:c.370T>A, XM_017015244.3:c.259T>C, XM_017015244.3:c.259T>A, XM_017015244.2:c.259T>C, XM_017015244.2:c.259T>A, XM_017015244.1:c.259T>C, XM_017015244.1:c.259T>A, XM_017015241.3:c.301T>C, XM_017015241.3:c.301T>A, XM_017015241.2:c.301T>C, XM_017015241.2:c.301T>A, XM_017015241.1:c.649T>C, XM_017015241.1:c.649T>A, XM_017015247.3:c.259T>C, XM_017015247.3:c.259T>A, XM_017015247.2:c.259T>C, XM_017015247.2:c.259T>A, XM_017015247.1:c.259T>C, XM_017015247.1:c.259T>A, NM_001077181.3:c.259T>C, NM_001077181.3:c.259T>A, NM_001077181.2:c.259T>C, NM_001077181.2:c.259T>A, NM_001077181.1:c.259T>C, NM_001077181.1:c.259T>A, NM_001351567.3:c.370T>C, NM_001351567.3:c.370T>A, NM_001351567.2:c.370T>C, NM_001351567.2:c.370T>A, NM_001351567.1:c.370T>C, NM_001351567.1:c.370T>A, NM_001351568.3:c.259T>C, NM_001351568.3:c.259T>A, NM_001351568.2:c.259T>C, NM_001351568.2:c.259T>A, NM_001351568.1:c.259T>C, NM_001351568.1:c.259T>A, XR_001746406.3:n.448T>C, XR_001746406.3:n.448T>A, XR_001746406.2:n.303T>C, XR_001746406.2:n.303T>A, XR_001746406.1:n.766T>C, XR_001746406.1:n.766T>A, NR_147239.2:n.835T>C, NR_147239.2:n.835T>A, NR_147239.1:n.822T>C, NR_147239.1:n.822T>A, NM_001351569.2:c.259T>C, NM_001351569.2:c.259T>A, NM_001351569.1:c.259T>C, NM_001351569.1:c.259T>A, XM_017015245.2:c.352T>C, XM_017015245.2:c.352T>A, XM_017015245.1:c.352T>C, XM_017015245.1:c.352T>A, XM_047424001.1:c.85T>C, XM_047424001.1:c.85T>A, XM_047424003.1:c.85T>C, XM_047424003.1:c.85T>A, XM_047424002.1:c.85T>C, XM_047424002.1:c.85T>A, XM_047424004.1:c.85T>C, XM_047424004.1:c.85T>A, XM_047424000.1:c.370T>C, XM_047424000.1:c.370T>A, NM_001351570.1:c.301T>C, NM_001351570.1:c.301T>A, NM_033332.1:c.370T>C, NM_033332.1:c.370T>A, XM_047424005.1:c.-121T>C, XM_047424005.1:c.-121T>A, XR_007061367.1:n.448T>C, XR_007061367.1:n.448T>A, XR_007061366.1:n.448T>C, XR_007061366.1:n.448T>A, XM_047423999.1:c.370T>C, XM_047423999.1:c.370T>A, XM_047423998.1:c.370T>C, XM_047423998.1:c.370T>A, XM_047423997.1:c.301T>C, XM_047423997.1:c.301T>A, NP_003662.1:p.Ser124Pro, NP_003662.1:p.Ser124Thr, XP_011517458.2:p.Ser118Pro, XP_011517458.2:p.Ser118Thr, NP_201588.1:p.Ser124Pro, NP_201588.1:p.Ser124Thr, XP_011517450.2:p.Ser101Pro, XP_011517450.2:p.Ser101Thr, XP_011517455.2:p.Ser101Pro, XP_011517455.2:p.Ser101Thr, XP_011517449.2:p.Ser101Pro, XP_011517449.2:p.Ser101Thr, XP_011517453.2:p.Ser101Pro, XP_011517453.2:p.Ser101Thr, XP_011517451.2:p.Ser101Pro, XP_011517451.2:p.Ser101Thr, XP_016870731.1:p.Ser124Pro, XP_016870731.1:p.Ser124Thr, XP_016870729.2:p.Ser101Pro, XP_016870729.2:p.Ser101Thr, XP_016870737.1:p.Ser124Pro, XP_016870737.1:p.Ser124Thr, XP_016870733.1:p.Ser87Pro, XP_016870733.1:p.Ser87Thr, XP_016870730.2:p.Ser101Pro, XP_016870730.2:p.Ser101Thr, XP_016870736.1:p.Ser87Pro, XP_016870736.1:p.Ser87Thr, NP_001070649.1:p.Ser87Pro, NP_001070649.1:p.Ser87Thr, NP_001338496.1:p.Ser124Pro, NP_001338496.1:p.Ser124Thr, NP_001338497.1:p.Ser87Pro, NP_001338497.1:p.Ser87Thr, NP_001338498.1:p.Ser87Pro, NP_001338498.1:p.Ser87Thr, XP_016870734.1:p.Ser118Pro, XP_016870734.1:p.Ser118Thr, XP_047279957.1:p.Ser29Pro, XP_047279957.1:p.Ser29Thr, XP_047279959.1:p.Ser29Pro, XP_047279959.1:p.Ser29Thr, XP_047279958.1:p.Ser29Pro, XP_047279958.1:p.Ser29Thr, XP_047279960.1:p.Ser29Pro, XP_047279960.1:p.Ser29Thr, XP_047279956.1:p.Ser124Pro, XP_047279956.1:p.Ser124Thr, NP_001338499.1:p.Ser101Pro, NP_001338499.1:p.Ser101Thr, XP_047279955.1:p.Ser124Pro, XP_047279955.1:p.Ser124Thr, XP_047279954.1:p.Ser124Pro, XP_047279954.1:p.Ser124Thr, XP_047279953.1:p.Ser101Pro, XP_047279953.1:p.Ser101Thr

                  9.

                  rs1472058205 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    A>C [Show Flanks]
                    Chromosome:
                    9:96533988 (GRCh38)
                    9:99296270 (GRCh37)
                    Canonical SPDI:
                    NC_000009.12:96533987:A:C
                    Gene:
                    CDC14B (Varview)
                    Functional Consequence:
                    coding_sequence_variant,non_coding_transcript_variant,missense_variant
                    Validated:
                    by frequency
                    MAF:
                    C=0.000004/1 (GnomAD_exomes)
                    HGVS:
                    NC_000009.12:g.96533988A>C, NC_000009.11:g.99296270A>C, NM_003671.5:c.885T>G, NM_003671.4:c.885T>G, NM_003671.3:c.885T>G, XM_011519156.4:c.867T>G, XM_011519156.3:c.867T>G, XM_011519156.2:c.867T>G, XM_011519156.1:c.867T>G, NM_033331.4:c.885T>G, NM_033331.3:c.885T>G, NM_033331.2:c.885T>G, XM_011519148.4:c.816T>G, XM_011519148.3:c.816T>G, XM_011519148.2:c.1164T>G, XM_011519148.1:c.1164T>G, XM_011519153.4:c.816T>G, XM_011519153.3:c.816T>G, XM_011519153.2:c.1164T>G, XM_011519153.1:c.1164T>G, XR_929864.4:n.963T>G, XR_929864.3:n.818T>G, XR_929864.2:n.1284T>G, XR_929864.1:n.1179T>G, XM_011519147.4:c.816T>G, XM_011519147.3:c.816T>G, XM_011519147.2:c.1164T>G, XM_011519147.1:c.1164T>G, XR_929865.4:n.963T>G, XR_929865.3:n.818T>G, XR_929865.2:n.1284T>G, XR_929865.1:n.1179T>G, XM_011519151.4:c.816T>G, XM_011519151.3:c.816T>G, XM_011519151.2:c.1164T>G, XM_011519151.1:c.1164T>G, XM_011519149.4:c.816T>G, XM_011519149.3:c.816T>G, XM_011519149.2:c.1164T>G, XM_011519149.1:c.1164T>G, XM_017015242.3:c.885T>G, XM_017015242.2:c.885T>G, XM_017015242.1:c.885T>G, XM_017015240.3:c.816T>G, XM_017015240.2:c.816T>G, XM_017015240.1:c.1164T>G, XM_017015248.3:c.678T>G, XM_017015248.2:c.678T>G, XM_017015248.1:c.678T>G, XM_017015244.3:c.774T>G, XM_017015244.2:c.774T>G, XM_017015244.1:c.774T>G, XM_017015241.3:c.609T>G, XM_017015241.2:c.609T>G, XM_017015241.1:c.957T>G, XM_017015247.3:c.774T>G, XM_017015247.2:c.774T>G, XM_017015247.1:c.774T>G, NM_001077181.3:c.774T>G, NM_001077181.2:c.774T>G, NM_001077181.1:c.774T>G, NM_001351567.3:c.885T>G, NM_001351567.2:c.885T>G, NM_001351567.1:c.885T>G, NM_001351568.3:c.774T>G, NM_001351568.2:c.774T>G, NM_001351568.1:c.774T>G, XR_001746406.3:n.963T>G, XR_001746406.2:n.818T>G, XR_001746406.1:n.1281T>G, NR_147239.2:n.1350T>G, NR_147239.1:n.1337T>G, NM_001351569.2:c.774T>G, NM_001351569.1:c.774T>G, XM_017015245.2:c.867T>G, XM_017015245.1:c.867T>G, XM_047424001.1:c.600T>G, XM_047424003.1:c.600T>G, XM_047424002.1:c.600T>G, XM_047424004.1:c.600T>G, XM_047424000.1:c.678T>G, NM_001351570.1:c.816T>G, NM_033332.1:c.885T>G, XM_047424005.1:c.318T>G, XM_047424006.1:c.87T>G, XR_007061367.1:n.963T>G, XR_007061366.1:n.963T>G, XM_047423999.1:c.885T>G, XM_047423998.1:c.885T>G, XM_047423997.1:c.816T>G, NP_003662.1:p.Ile295Met, XP_011517458.2:p.Ile289Met, NP_201588.1:p.Ile295Met, XP_011517450.2:p.Ile272Met, XP_011517455.2:p.Ile272Met, XP_011517449.2:p.Ile272Met, XP_011517453.2:p.Ile272Met, XP_011517451.2:p.Ile272Met, XP_016870731.1:p.Ile295Met, XP_016870729.2:p.Ile272Met, XP_016870737.1:p.Ile226Met, XP_016870733.1:p.Ile258Met, XP_016870730.2:p.Ile203Met, XP_016870736.1:p.Ile258Met, NP_001070649.1:p.Ile258Met, NP_001338496.1:p.Ile295Met, NP_001338497.1:p.Ile258Met, NP_001338498.1:p.Ile258Met, XP_016870734.1:p.Ile289Met, XP_047279957.1:p.Ile200Met, XP_047279959.1:p.Ile200Met, XP_047279958.1:p.Ile200Met, XP_047279960.1:p.Ile200Met, XP_047279956.1:p.Ile226Met, NP_001338499.1:p.Ile272Met, XP_047279961.1:p.Ile106Met, XP_047279962.1:p.Ile29Met, XP_047279955.1:p.Ile295Met, XP_047279954.1:p.Ile295Met, XP_047279953.1:p.Ile272Met

                    10.

                    rs1470388713 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      G>A,C [Show Flanks]
                      Chromosome:
                      9:96522506 (GRCh38)
                      9:99284788 (GRCh37)
                      Canonical SPDI:
                      NC_000009.12:96522505:G:A,NC_000009.12:96522505:G:C
                      Gene:
                      CDC14B (Varview)
                      Functional Consequence:
                      coding_sequence_variant,non_coding_transcript_variant,missense_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      A=0./0 (ALFA)
                      A=0.000007/1 (GnomAD)
                      A=0.000011/3 (TOPMED)
                      HGVS:
                      NC_000009.12:g.96522506G>A, NC_000009.12:g.96522506G>C, NC_000009.11:g.99284788G>A, NC_000009.11:g.99284788G>C, NM_003671.5:c.1343C>T, NM_003671.5:c.1343C>G, NM_003671.4:c.1343C>T, NM_003671.4:c.1343C>G, NM_003671.3:c.1343C>T, NM_003671.3:c.1343C>G, XM_011519156.4:c.1325C>T, XM_011519156.4:c.1325C>G, XM_011519156.3:c.1325C>T, XM_011519156.3:c.1325C>G, XM_011519156.2:c.1325C>T, XM_011519156.2:c.1325C>G, XM_011519156.1:c.1325C>T, XM_011519156.1:c.1325C>G, NM_033331.4:c.1343C>T, NM_033331.4:c.1343C>G, NM_033331.3:c.1343C>T, NM_033331.3:c.1343C>G, NM_033331.2:c.1343C>T, NM_033331.2:c.1343C>G, XM_011519148.4:c.1274C>T, XM_011519148.4:c.1274C>G, XM_011519148.3:c.1274C>T, XM_011519148.3:c.1274C>G, XM_011519148.2:c.1622C>T, XM_011519148.2:c.1622C>G, XM_011519148.1:c.1622C>T, XM_011519148.1:c.1622C>G, XM_011519153.4:c.1274C>T, XM_011519153.4:c.1274C>G, XM_011519153.3:c.1274C>T, XM_011519153.3:c.1274C>G, XM_011519153.2:c.1622C>T, XM_011519153.2:c.1622C>G, XM_011519153.1:c.1622C>T, XM_011519153.1:c.1622C>G, XR_929864.4:n.1421C>T, XR_929864.4:n.1421C>G, XR_929864.3:n.1276C>T, XR_929864.3:n.1276C>G, XR_929864.2:n.1742C>T, XR_929864.2:n.1742C>G, XR_929864.1:n.1637C>T, XR_929864.1:n.1637C>G, XM_011519147.4:c.1274C>T, XM_011519147.4:c.1274C>G, XM_011519147.3:c.1274C>T, XM_011519147.3:c.1274C>G, XM_011519147.2:c.1622C>T, XM_011519147.2:c.1622C>G, XM_011519147.1:c.1622C>T, XM_011519147.1:c.1622C>G, XR_929865.4:n.1421C>T, XR_929865.4:n.1421C>G, XR_929865.3:n.1276C>T, XR_929865.3:n.1276C>G, XR_929865.2:n.1742C>T, XR_929865.2:n.1742C>G, XR_929865.1:n.1637C>T, XR_929865.1:n.1637C>G, XM_011519151.4:c.1274C>T, XM_011519151.4:c.1274C>G, XM_011519151.3:c.1274C>T, XM_011519151.3:c.1274C>G, XM_011519151.2:c.1622C>T, XM_011519151.2:c.1622C>G, XM_011519151.1:c.1622C>T, XM_011519151.1:c.1622C>G, XM_011519149.4:c.1274C>T, XM_011519149.4:c.1274C>G, XM_011519149.3:c.1274C>T, XM_011519149.3:c.1274C>G, XM_011519149.2:c.1622C>T, XM_011519149.2:c.1622C>G, XM_011519149.1:c.1622C>T, XM_011519149.1:c.1622C>G, XM_017015242.3:c.1343C>T, XM_017015242.3:c.1343C>G, XM_017015242.2:c.1343C>T, XM_017015242.2:c.1343C>G, XM_017015242.1:c.1343C>T, XM_017015242.1:c.1343C>G, XM_017015240.3:c.1274C>T, XM_017015240.3:c.1274C>G, XM_017015240.2:c.1274C>T, XM_017015240.2:c.1274C>G, XM_017015240.1:c.1622C>T, XM_017015240.1:c.1622C>G, XM_017015248.3:c.1136C>T, XM_017015248.3:c.1136C>G, XM_017015248.2:c.1136C>T, XM_017015248.2:c.1136C>G, XM_017015248.1:c.1136C>T, XM_017015248.1:c.1136C>G, XM_017015244.3:c.1232C>T, XM_017015244.3:c.1232C>G, XM_017015244.2:c.1232C>T, XM_017015244.2:c.1232C>G, XM_017015244.1:c.1232C>T, XM_017015244.1:c.1232C>G, XM_017015241.3:c.1067C>T, XM_017015241.3:c.1067C>G, XM_017015241.2:c.1067C>T, XM_017015241.2:c.1067C>G, XM_017015241.1:c.1415C>T, XM_017015241.1:c.1415C>G, XM_017015247.3:c.1232C>T, XM_017015247.3:c.1232C>G, XM_017015247.2:c.1232C>T, XM_017015247.2:c.1232C>G, XM_017015247.1:c.1232C>T, XM_017015247.1:c.1232C>G, NM_001077181.3:c.1232C>T, NM_001077181.3:c.1232C>G, NM_001077181.2:c.1232C>T, NM_001077181.2:c.1232C>G, NM_001077181.1:c.1232C>T, NM_001077181.1:c.1232C>G, NM_001351567.3:c.1343C>T, NM_001351567.3:c.1343C>G, NM_001351567.2:c.1343C>T, NM_001351567.2:c.1343C>G, NM_001351567.1:c.1343C>T, NM_001351567.1:c.1343C>G, NM_001351568.3:c.1232C>T, NM_001351568.3:c.1232C>G, NM_001351568.2:c.1232C>T, NM_001351568.2:c.1232C>G, NM_001351568.1:c.1232C>T, NM_001351568.1:c.1232C>G, XR_001746406.3:n.1421C>T, XR_001746406.3:n.1421C>G, XR_001746406.2:n.1276C>T, XR_001746406.2:n.1276C>G, XR_001746406.1:n.1739C>T, XR_001746406.1:n.1739C>G, NR_147239.2:n.1808C>T, NR_147239.2:n.1808C>G, NR_147239.1:n.1795C>T, NR_147239.1:n.1795C>G, NM_001351569.2:c.1232C>T, NM_001351569.2:c.1232C>G, NM_001351569.1:c.1232C>T, NM_001351569.1:c.1232C>G, XM_017015245.2:c.1325C>T, XM_017015245.2:c.1325C>G, XM_017015245.1:c.1325C>T, XM_017015245.1:c.1325C>G, XM_047424001.1:c.1058C>T, XM_047424001.1:c.1058C>G, XM_047424003.1:c.1058C>T, XM_047424003.1:c.1058C>G, XM_047424002.1:c.1058C>T, XM_047424002.1:c.1058C>G, XM_047424004.1:c.1058C>T, XM_047424004.1:c.1058C>G, XM_047424000.1:c.1136C>T, XM_047424000.1:c.1136C>G, NM_001351570.1:c.1274C>T, NM_001351570.1:c.1274C>G, NM_033332.1:c.1343C>T, NM_033332.1:c.1343C>G, XM_047424005.1:c.776C>T, XM_047424005.1:c.776C>G, XM_047424006.1:c.545C>T, XM_047424006.1:c.545C>G, XR_007061367.1:n.1421C>T, XR_007061367.1:n.1421C>G, XR_007061366.1:n.1421C>T, XR_007061366.1:n.1421C>G, XM_047423999.1:c.1343C>T, XM_047423999.1:c.1343C>G, XM_047423998.1:c.1343C>T, XM_047423998.1:c.1343C>G, XM_047423997.1:c.1274C>T, XM_047423997.1:c.1274C>G, NP_003662.1:p.Thr448Ile, NP_003662.1:p.Thr448Ser, XP_011517458.2:p.Thr442Ile, XP_011517458.2:p.Thr442Arg, NP_201588.1:p.Thr448Ile, NP_201588.1:p.Thr448Arg, XP_011517450.2:p.Thr425Ile, XP_011517450.2:p.Thr425Arg, XP_011517455.2:p.Thr425Ile, XP_011517455.2:p.Thr425Ser, XP_011517449.2:p.Thr425Ile, XP_011517449.2:p.Thr425Arg, XP_011517453.2:p.Thr425Ile, XP_011517453.2:p.Thr425Arg, XP_011517451.2:p.Thr425Ile, XP_011517451.2:p.Thr425Arg, XP_016870731.1:p.Thr448Ile, XP_016870731.1:p.Thr448Arg, XP_016870729.2:p.Thr425Ile, XP_016870729.2:p.Thr425Arg, XP_016870737.1:p.Thr379Ile, XP_016870737.1:p.Thr379Ser, XP_016870733.1:p.Thr411Ile, XP_016870733.1:p.Thr411Arg, XP_016870730.2:p.Thr356Ile, XP_016870730.2:p.Thr356Arg, XP_016870736.1:p.Thr411Ile, XP_016870736.1:p.Thr411Ser, NP_001070649.1:p.Thr411Ile, NP_001070649.1:p.Thr411Arg, NP_001338496.1:p.Thr448Ile, NP_001338496.1:p.Thr448Arg, NP_001338497.1:p.Thr411Ile, NP_001338497.1:p.Thr411Arg, NP_001338498.1:p.Thr411Ile, NP_001338498.1:p.Thr411Arg, XP_016870734.1:p.Thr442Ile, XP_016870734.1:p.Thr442Arg, XP_047279957.1:p.Thr353Ile, XP_047279957.1:p.Thr353Arg, XP_047279959.1:p.Thr353Ile, XP_047279959.1:p.Thr353Arg, XP_047279958.1:p.Thr353Ile, XP_047279958.1:p.Thr353Arg, XP_047279960.1:p.Thr353Ile, XP_047279960.1:p.Thr353Ser, XP_047279956.1:p.Thr379Ile, XP_047279956.1:p.Thr379Arg, NP_001338499.1:p.Thr425Ile, NP_001338499.1:p.Thr425Arg, XP_047279961.1:p.Thr259Ile, XP_047279961.1:p.Thr259Arg, XP_047279962.1:p.Thr182Ile, XP_047279962.1:p.Thr182Arg, XP_047279955.1:p.Thr448Ile, XP_047279955.1:p.Thr448Ser, XP_047279954.1:p.Thr448Ile, XP_047279954.1:p.Thr448Arg, XP_047279953.1:p.Thr425Ile, XP_047279953.1:p.Thr425Arg

                      11.

                      rs1468077768 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        G>A [Show Flanks]
                        Chromosome:
                        9:96534006 (GRCh38)
                        9:99296288 (GRCh37)
                        Canonical SPDI:
                        NC_000009.12:96534005:G:A
                        Gene:
                        CDC14B (Varview)
                        Functional Consequence:
                        coding_sequence_variant,synonymous_variant,non_coding_transcript_variant
                        Validated:
                        by frequency,by alfa
                        MAF:
                        A=0./0 (ALFA)
                        HGVS:
                        NC_000009.12:g.96534006G>A, NC_000009.11:g.99296288G>A, NM_003671.5:c.867C>T, NM_003671.4:c.867C>T, NM_003671.3:c.867C>T, XM_011519156.4:c.849C>T, XM_011519156.3:c.849C>T, XM_011519156.2:c.849C>T, XM_011519156.1:c.849C>T, NM_033331.4:c.867C>T, NM_033331.3:c.867C>T, NM_033331.2:c.867C>T, XM_011519148.4:c.798C>T, XM_011519148.3:c.798C>T, XM_011519148.2:c.1146C>T, XM_011519148.1:c.1146C>T, XM_011519153.4:c.798C>T, XM_011519153.3:c.798C>T, XM_011519153.2:c.1146C>T, XM_011519153.1:c.1146C>T, XR_929864.4:n.945C>T, XR_929864.3:n.800C>T, XR_929864.2:n.1266C>T, XR_929864.1:n.1161C>T, XM_011519147.4:c.798C>T, XM_011519147.3:c.798C>T, XM_011519147.2:c.1146C>T, XM_011519147.1:c.1146C>T, XR_929865.4:n.945C>T, XR_929865.3:n.800C>T, XR_929865.2:n.1266C>T, XR_929865.1:n.1161C>T, XM_011519151.4:c.798C>T, XM_011519151.3:c.798C>T, XM_011519151.2:c.1146C>T, XM_011519151.1:c.1146C>T, XM_011519149.4:c.798C>T, XM_011519149.3:c.798C>T, XM_011519149.2:c.1146C>T, XM_011519149.1:c.1146C>T, XM_017015242.3:c.867C>T, XM_017015242.2:c.867C>T, XM_017015242.1:c.867C>T, XM_017015240.3:c.798C>T, XM_017015240.2:c.798C>T, XM_017015240.1:c.1146C>T, XM_017015248.3:c.660C>T, XM_017015248.2:c.660C>T, XM_017015248.1:c.660C>T, XM_017015244.3:c.756C>T, XM_017015244.2:c.756C>T, XM_017015244.1:c.756C>T, XM_017015241.3:c.591C>T, XM_017015241.2:c.591C>T, XM_017015241.1:c.939C>T, XM_017015247.3:c.756C>T, XM_017015247.2:c.756C>T, XM_017015247.1:c.756C>T, NM_001077181.3:c.756C>T, NM_001077181.2:c.756C>T, NM_001077181.1:c.756C>T, NM_001351567.3:c.867C>T, NM_001351567.2:c.867C>T, NM_001351567.1:c.867C>T, NM_001351568.3:c.756C>T, NM_001351568.2:c.756C>T, NM_001351568.1:c.756C>T, XR_001746406.3:n.945C>T, XR_001746406.2:n.800C>T, XR_001746406.1:n.1263C>T, NR_147239.2:n.1332C>T, NR_147239.1:n.1319C>T, NM_001351569.2:c.756C>T, NM_001351569.1:c.756C>T, XM_017015245.2:c.849C>T, XM_017015245.1:c.849C>T, XM_047424001.1:c.582C>T, XM_047424003.1:c.582C>T, XM_047424002.1:c.582C>T, XM_047424004.1:c.582C>T, XM_047424000.1:c.660C>T, NM_001351570.1:c.798C>T, NM_033332.1:c.867C>T, XM_047424005.1:c.300C>T, XM_047424006.1:c.69C>T, XR_007061367.1:n.945C>T, XR_007061366.1:n.945C>T, XM_047423999.1:c.867C>T, XM_047423998.1:c.867C>T, XM_047423997.1:c.798C>T

                        12.

                        rs1463101620 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          C>G [Show Flanks]
                          Chromosome:
                          9:96619271 (GRCh38)
                          9:99381553 (GRCh37)
                          Canonical SPDI:
                          NC_000009.12:96619270:C:G
                          Gene:
                          CDC14B (Varview)
                          Functional Consequence:
                          missense_variant,coding_sequence_variant,genic_upstream_transcript_variant,non_coding_transcript_variant,5_prime_UTR_variant,upstream_transcript_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          G=0./0 (ALFA)
                          G=0.000029/4 (GnomAD)
                          G=0.000087/23 (TOPMED)
                          HGVS:
                          NC_000009.12:g.96619271C>G, NC_000009.11:g.99381553C>G, NM_003671.5:c.108G>C, NM_003671.4:c.108G>C, NM_003671.3:c.108G>C, NM_033331.4:c.108G>C, NM_033331.3:c.108G>C, NM_033331.2:c.108G>C, XM_017015242.3:c.108G>C, XM_017015242.2:c.108G>C, XM_017015242.1:c.108G>C, XM_017015248.3:c.108G>C, XM_017015248.2:c.108G>C, XM_017015248.1:c.108G>C, NM_001351567.3:c.108G>C, NM_001351567.2:c.108G>C, NM_001351567.1:c.108G>C, NR_147239.2:n.573G>C, NR_147239.1:n.560G>C, XM_047424001.1:c.-207G>C, XM_047424003.1:c.-207G>C, XM_047424004.1:c.-207G>C, XM_047424000.1:c.108G>C, NM_033332.1:c.108G>C, XM_047423999.1:c.108G>C, XM_047423998.1:c.108G>C, NP_003662.1:p.Gln36His, NP_201588.1:p.Gln36His, XP_016870731.1:p.Gln36His, XP_016870737.1:p.Gln36His, NP_001338496.1:p.Gln36His, XP_047279956.1:p.Gln36His, XP_047279955.1:p.Gln36His, XP_047279954.1:p.Gln36His

                          13.

                          rs1462723221 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            C>T [Show Flanks]
                            Chromosome:
                            9:96619317 (GRCh38)
                            9:99381599 (GRCh37)
                            Canonical SPDI:
                            NC_000009.12:96619316:C:T
                            Gene:
                            CDC14B (Varview)
                            Functional Consequence:
                            missense_variant,coding_sequence_variant,genic_upstream_transcript_variant,non_coding_transcript_variant,5_prime_UTR_variant,upstream_transcript_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            T=0./0 (ALFA)
                            T=0.000007/1 (GnomAD)
                            HGVS:
                            NC_000009.12:g.96619317C>T, NC_000009.11:g.99381599C>T, NM_003671.5:c.62G>A, NM_003671.4:c.62G>A, NM_003671.3:c.62G>A, NM_033331.4:c.62G>A, NM_033331.3:c.62G>A, NM_033331.2:c.62G>A, XM_017015242.3:c.62G>A, XM_017015242.2:c.62G>A, XM_017015242.1:c.62G>A, XM_017015248.3:c.62G>A, XM_017015248.2:c.62G>A, XM_017015248.1:c.62G>A, NM_001351567.3:c.62G>A, NM_001351567.2:c.62G>A, NM_001351567.1:c.62G>A, NR_147239.2:n.527G>A, NR_147239.1:n.514G>A, XM_047424001.1:c.-253G>A, XM_047424003.1:c.-253G>A, XM_047424004.1:c.-253G>A, XM_047424000.1:c.62G>A, NM_033332.1:c.62G>A, XM_047423999.1:c.62G>A, XM_047423998.1:c.62G>A, NP_003662.1:p.Cys21Tyr, NP_201588.1:p.Cys21Tyr, XP_016870731.1:p.Cys21Tyr, XP_016870737.1:p.Cys21Tyr, NP_001338496.1:p.Cys21Tyr, XP_047279956.1:p.Cys21Tyr, XP_047279955.1:p.Cys21Tyr, XP_047279954.1:p.Cys21Tyr

                            14.

                            rs1458889702 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              T>C [Show Flanks]
                              Chromosome:
                              9:96551806 (GRCh38)
                              9:99314088 (GRCh37)
                              Canonical SPDI:
                              NC_000009.12:96551805:T:C
                              Gene:
                              CDC14B (Varview)
                              Functional Consequence:
                              missense_variant,intron_variant,coding_sequence_variant,non_coding_transcript_variant,genic_upstream_transcript_variant
                              Validated:
                              by frequency
                              MAF:
                              C=0.000004/1 (GnomAD_exomes)
                              HGVS:
                              NC_000009.12:g.96551806T>C, NC_000009.11:g.99314088T>C, NM_003671.5:c.487A>G, NM_003671.4:c.487A>G, NM_003671.3:c.487A>G, XM_011519156.4:c.469A>G, XM_011519156.3:c.469A>G, XM_011519156.2:c.469A>G, XM_011519156.1:c.469A>G, NM_033331.4:c.487A>G, NM_033331.3:c.487A>G, NM_033331.2:c.487A>G, XM_011519148.4:c.418A>G, XM_011519148.3:c.418A>G, XM_011519148.2:c.766A>G, XM_011519148.1:c.766A>G, XM_011519153.4:c.418A>G, XM_011519153.3:c.418A>G, XM_011519153.2:c.766A>G, XM_011519153.1:c.766A>G, XR_929864.4:n.565A>G, XR_929864.3:n.420A>G, XR_929864.2:n.886A>G, XR_929864.1:n.781A>G, XM_011519147.4:c.418A>G, XM_011519147.3:c.418A>G, XM_011519147.2:c.766A>G, XM_011519147.1:c.766A>G, XR_929865.4:n.565A>G, XR_929865.3:n.420A>G, XR_929865.2:n.886A>G, XR_929865.1:n.781A>G, XM_011519151.4:c.418A>G, XM_011519151.3:c.418A>G, XM_011519151.2:c.766A>G, XM_011519151.1:c.766A>G, XM_011519149.4:c.418A>G, XM_011519149.3:c.418A>G, XM_011519149.2:c.766A>G, XM_011519149.1:c.766A>G, XM_017015242.3:c.487A>G, XM_017015242.2:c.487A>G, XM_017015242.1:c.487A>G, XM_017015240.3:c.418A>G, XM_017015240.2:c.418A>G, XM_017015240.1:c.766A>G, XM_017015244.3:c.376A>G, XM_017015244.2:c.376A>G, XM_017015244.1:c.376A>G, XM_017015247.3:c.376A>G, XM_017015247.2:c.376A>G, XM_017015247.1:c.376A>G, NM_001077181.3:c.376A>G, NM_001077181.2:c.376A>G, NM_001077181.1:c.376A>G, NM_001351567.3:c.487A>G, NM_001351567.2:c.487A>G, NM_001351567.1:c.487A>G, NM_001351568.3:c.376A>G, NM_001351568.2:c.376A>G, NM_001351568.1:c.376A>G, XR_001746406.3:n.565A>G, XR_001746406.2:n.420A>G, XR_001746406.1:n.883A>G, NR_147239.2:n.952A>G, NR_147239.1:n.939A>G, NM_001351569.2:c.376A>G, NM_001351569.1:c.376A>G, XM_017015245.2:c.469A>G, XM_017015245.1:c.469A>G, XM_047424001.1:c.202A>G, XM_047424003.1:c.202A>G, XM_047424002.1:c.202A>G, XM_047424004.1:c.202A>G, NM_001351570.1:c.418A>G, NM_033332.1:c.487A>G, XR_007061367.1:n.565A>G, XR_007061366.1:n.565A>G, XM_047423999.1:c.487A>G, XM_047423998.1:c.487A>G, XM_047423997.1:c.418A>G, NP_003662.1:p.Ile163Val, XP_011517458.2:p.Ile157Val, NP_201588.1:p.Ile163Val, XP_011517450.2:p.Ile140Val, XP_011517455.2:p.Ile140Val, XP_011517449.2:p.Ile140Val, XP_011517453.2:p.Ile140Val, XP_011517451.2:p.Ile140Val, XP_016870731.1:p.Ile163Val, XP_016870729.2:p.Ile140Val, XP_016870733.1:p.Ile126Val, XP_016870736.1:p.Ile126Val, NP_001070649.1:p.Ile126Val, NP_001338496.1:p.Ile163Val, NP_001338497.1:p.Ile126Val, NP_001338498.1:p.Ile126Val, XP_016870734.1:p.Ile157Val, XP_047279957.1:p.Ile68Val, XP_047279959.1:p.Ile68Val, XP_047279958.1:p.Ile68Val, XP_047279960.1:p.Ile68Val, NP_001338499.1:p.Ile140Val, XP_047279955.1:p.Ile163Val, XP_047279954.1:p.Ile163Val, XP_047279953.1:p.Ile140Val

                              15.

                              rs1456517473 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                A>G [Show Flanks]
                                Chromosome:
                                9:96551812 (GRCh38)
                                9:99314094 (GRCh37)
                                Canonical SPDI:
                                NC_000009.12:96551811:A:G
                                Gene:
                                CDC14B (Varview)
                                Functional Consequence:
                                missense_variant,intron_variant,coding_sequence_variant,non_coding_transcript_variant,genic_upstream_transcript_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                G=0./0 (ALFA)
                                G=0.000007/1 (GnomAD)
                                G=0.000015/4 (TOPMED)
                                HGVS:
                                NC_000009.12:g.96551812A>G, NC_000009.11:g.99314094A>G, NM_003671.5:c.481T>C, NM_003671.4:c.481T>C, NM_003671.3:c.481T>C, XM_011519156.4:c.463T>C, XM_011519156.3:c.463T>C, XM_011519156.2:c.463T>C, XM_011519156.1:c.463T>C, NM_033331.4:c.481T>C, NM_033331.3:c.481T>C, NM_033331.2:c.481T>C, XM_011519148.4:c.412T>C, XM_011519148.3:c.412T>C, XM_011519148.2:c.760T>C, XM_011519148.1:c.760T>C, XM_011519153.4:c.412T>C, XM_011519153.3:c.412T>C, XM_011519153.2:c.760T>C, XM_011519153.1:c.760T>C, XR_929864.4:n.559T>C, XR_929864.3:n.414T>C, XR_929864.2:n.880T>C, XR_929864.1:n.775T>C, XM_011519147.4:c.412T>C, XM_011519147.3:c.412T>C, XM_011519147.2:c.760T>C, XM_011519147.1:c.760T>C, XR_929865.4:n.559T>C, XR_929865.3:n.414T>C, XR_929865.2:n.880T>C, XR_929865.1:n.775T>C, XM_011519151.4:c.412T>C, XM_011519151.3:c.412T>C, XM_011519151.2:c.760T>C, XM_011519151.1:c.760T>C, XM_011519149.4:c.412T>C, XM_011519149.3:c.412T>C, XM_011519149.2:c.760T>C, XM_011519149.1:c.760T>C, XM_017015242.3:c.481T>C, XM_017015242.2:c.481T>C, XM_017015242.1:c.481T>C, XM_017015240.3:c.412T>C, XM_017015240.2:c.412T>C, XM_017015240.1:c.760T>C, XM_017015244.3:c.370T>C, XM_017015244.2:c.370T>C, XM_017015244.1:c.370T>C, XM_017015247.3:c.370T>C, XM_017015247.2:c.370T>C, XM_017015247.1:c.370T>C, NM_001077181.3:c.370T>C, NM_001077181.2:c.370T>C, NM_001077181.1:c.370T>C, NM_001351567.3:c.481T>C, NM_001351567.2:c.481T>C, NM_001351567.1:c.481T>C, NM_001351568.3:c.370T>C, NM_001351568.2:c.370T>C, NM_001351568.1:c.370T>C, XR_001746406.3:n.559T>C, XR_001746406.2:n.414T>C, XR_001746406.1:n.877T>C, NR_147239.2:n.946T>C, NR_147239.1:n.933T>C, NM_001351569.2:c.370T>C, NM_001351569.1:c.370T>C, XM_017015245.2:c.463T>C, XM_017015245.1:c.463T>C, XM_047424001.1:c.196T>C, XM_047424003.1:c.196T>C, XM_047424002.1:c.196T>C, XM_047424004.1:c.196T>C, NM_001351570.1:c.412T>C, NM_033332.1:c.481T>C, XR_007061367.1:n.559T>C, XR_007061366.1:n.559T>C, XM_047423999.1:c.481T>C, XM_047423998.1:c.481T>C, XM_047423997.1:c.412T>C, NP_003662.1:p.Ser161Pro, XP_011517458.2:p.Ser155Pro, NP_201588.1:p.Ser161Pro, XP_011517450.2:p.Ser138Pro, XP_011517455.2:p.Ser138Pro, XP_011517449.2:p.Ser138Pro, XP_011517453.2:p.Ser138Pro, XP_011517451.2:p.Ser138Pro, XP_016870731.1:p.Ser161Pro, XP_016870729.2:p.Ser138Pro, XP_016870733.1:p.Ser124Pro, XP_016870736.1:p.Ser124Pro, NP_001070649.1:p.Ser124Pro, NP_001338496.1:p.Ser161Pro, NP_001338497.1:p.Ser124Pro, NP_001338498.1:p.Ser124Pro, XP_016870734.1:p.Ser155Pro, XP_047279957.1:p.Ser66Pro, XP_047279959.1:p.Ser66Pro, XP_047279958.1:p.Ser66Pro, XP_047279960.1:p.Ser66Pro, NP_001338499.1:p.Ser138Pro, XP_047279955.1:p.Ser161Pro, XP_047279954.1:p.Ser161Pro, XP_047279953.1:p.Ser138Pro

                                16.

                                rs1453678262 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  T>C [Show Flanks]
                                  Chromosome:
                                  9:96534505 (GRCh38)
                                  9:99296787 (GRCh37)
                                  Canonical SPDI:
                                  NC_000009.12:96534504:T:C
                                  Gene:
                                  CDC14B (Varview)
                                  Functional Consequence:
                                  coding_sequence_variant,non_coding_transcript_variant,missense_variant,5_prime_UTR_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  C=0./0 (ALFA)
                                  C=0.000004/1 (TOPMED)
                                  C=0.000007/1 (GnomAD)
                                  HGVS:
                                  NC_000009.12:g.96534505T>C, NC_000009.11:g.99296787T>C, NM_003671.5:c.665A>G, NM_003671.4:c.665A>G, NM_003671.3:c.665A>G, XM_011519156.4:c.647A>G, XM_011519156.3:c.647A>G, XM_011519156.2:c.647A>G, XM_011519156.1:c.647A>G, NM_033331.4:c.665A>G, NM_033331.3:c.665A>G, NM_033331.2:c.665A>G, XM_011519148.4:c.596A>G, XM_011519148.3:c.596A>G, XM_011519148.2:c.944A>G, XM_011519148.1:c.944A>G, XM_011519153.4:c.596A>G, XM_011519153.3:c.596A>G, XM_011519153.2:c.944A>G, XM_011519153.1:c.944A>G, XR_929864.4:n.743A>G, XR_929864.3:n.598A>G, XR_929864.2:n.1064A>G, XR_929864.1:n.959A>G, XM_011519147.4:c.596A>G, XM_011519147.3:c.596A>G, XM_011519147.2:c.944A>G, XM_011519147.1:c.944A>G, XR_929865.4:n.743A>G, XR_929865.3:n.598A>G, XR_929865.2:n.1064A>G, XR_929865.1:n.959A>G, XM_011519151.4:c.596A>G, XM_011519151.3:c.596A>G, XM_011519151.2:c.944A>G, XM_011519151.1:c.944A>G, XM_011519149.4:c.596A>G, XM_011519149.3:c.596A>G, XM_011519149.2:c.944A>G, XM_011519149.1:c.944A>G, XM_017015242.3:c.665A>G, XM_017015242.2:c.665A>G, XM_017015242.1:c.665A>G, XM_017015240.3:c.596A>G, XM_017015240.2:c.596A>G, XM_017015240.1:c.944A>G, XM_017015248.3:c.458A>G, XM_017015248.2:c.458A>G, XM_017015248.1:c.458A>G, XM_017015244.3:c.554A>G, XM_017015244.2:c.554A>G, XM_017015244.1:c.554A>G, XM_017015241.3:c.389A>G, XM_017015241.2:c.389A>G, XM_017015241.1:c.737A>G, XM_017015247.3:c.554A>G, XM_017015247.2:c.554A>G, XM_017015247.1:c.554A>G, NM_001077181.3:c.554A>G, NM_001077181.2:c.554A>G, NM_001077181.1:c.554A>G, NM_001351567.3:c.665A>G, NM_001351567.2:c.665A>G, NM_001351567.1:c.665A>G, NM_001351568.3:c.554A>G, NM_001351568.2:c.554A>G, NM_001351568.1:c.554A>G, XR_001746406.3:n.743A>G, XR_001746406.2:n.598A>G, XR_001746406.1:n.1061A>G, NR_147239.2:n.1130A>G, NR_147239.1:n.1117A>G, NM_001351569.2:c.554A>G, NM_001351569.1:c.554A>G, XM_017015245.2:c.647A>G, XM_017015245.1:c.647A>G, XM_047424001.1:c.380A>G, XM_047424003.1:c.380A>G, XM_047424002.1:c.380A>G, XM_047424004.1:c.380A>G, XM_047424000.1:c.458A>G, NM_001351570.1:c.596A>G, NM_033332.1:c.665A>G, XM_047424005.1:c.98A>G, XM_047424006.1:c.-134A>G, XR_007061367.1:n.743A>G, XR_007061366.1:n.743A>G, XM_047423999.1:c.665A>G, XM_047423998.1:c.665A>G, XM_047423997.1:c.596A>G, NP_003662.1:p.Asp222Gly, XP_011517458.2:p.Asp216Gly, NP_201588.1:p.Asp222Gly, XP_011517450.2:p.Asp199Gly, XP_011517455.2:p.Asp199Gly, XP_011517449.2:p.Asp199Gly, XP_011517453.2:p.Asp199Gly, XP_011517451.2:p.Asp199Gly, XP_016870731.1:p.Asp222Gly, XP_016870729.2:p.Asp199Gly, XP_016870737.1:p.Asp153Gly, XP_016870733.1:p.Asp185Gly, XP_016870730.2:p.Asp130Gly, XP_016870736.1:p.Asp185Gly, NP_001070649.1:p.Asp185Gly, NP_001338496.1:p.Asp222Gly, NP_001338497.1:p.Asp185Gly, NP_001338498.1:p.Asp185Gly, XP_016870734.1:p.Asp216Gly, XP_047279957.1:p.Asp127Gly, XP_047279959.1:p.Asp127Gly, XP_047279958.1:p.Asp127Gly, XP_047279960.1:p.Asp127Gly, XP_047279956.1:p.Asp153Gly, NP_001338499.1:p.Asp199Gly, XP_047279961.1:p.Asp33Gly, XP_047279955.1:p.Asp222Gly, XP_047279954.1:p.Asp222Gly, XP_047279953.1:p.Asp199Gly

                                  17.

                                  rs1447135175 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    G>A [Show Flanks]
                                    Chromosome:
                                    9:96534032 (GRCh38)
                                    9:99296314 (GRCh37)
                                    Canonical SPDI:
                                    NC_000009.12:96534031:G:A
                                    Gene:
                                    CDC14B (Varview)
                                    Functional Consequence:
                                    coding_sequence_variant,non_coding_transcript_variant,missense_variant
                                    Validated:
                                    by frequency
                                    MAF:
                                    A=0.000004/1 (GnomAD_exomes)
                                    HGVS:
                                    NC_000009.12:g.96534032G>A, NC_000009.11:g.99296314G>A, NM_003671.5:c.841C>T, NM_003671.4:c.841C>T, NM_003671.3:c.841C>T, XM_011519156.4:c.823C>T, XM_011519156.3:c.823C>T, XM_011519156.2:c.823C>T, XM_011519156.1:c.823C>T, NM_033331.4:c.841C>T, NM_033331.3:c.841C>T, NM_033331.2:c.841C>T, XM_011519148.4:c.772C>T, XM_011519148.3:c.772C>T, XM_011519148.2:c.1120C>T, XM_011519148.1:c.1120C>T, XM_011519153.4:c.772C>T, XM_011519153.3:c.772C>T, XM_011519153.2:c.1120C>T, XM_011519153.1:c.1120C>T, XR_929864.4:n.919C>T, XR_929864.3:n.774C>T, XR_929864.2:n.1240C>T, XR_929864.1:n.1135C>T, XM_011519147.4:c.772C>T, XM_011519147.3:c.772C>T, XM_011519147.2:c.1120C>T, XM_011519147.1:c.1120C>T, XR_929865.4:n.919C>T, XR_929865.3:n.774C>T, XR_929865.2:n.1240C>T, XR_929865.1:n.1135C>T, XM_011519151.4:c.772C>T, XM_011519151.3:c.772C>T, XM_011519151.2:c.1120C>T, XM_011519151.1:c.1120C>T, XM_011519149.4:c.772C>T, XM_011519149.3:c.772C>T, XM_011519149.2:c.1120C>T, XM_011519149.1:c.1120C>T, XM_017015242.3:c.841C>T, XM_017015242.2:c.841C>T, XM_017015242.1:c.841C>T, XM_017015240.3:c.772C>T, XM_017015240.2:c.772C>T, XM_017015240.1:c.1120C>T, XM_017015248.3:c.634C>T, XM_017015248.2:c.634C>T, XM_017015248.1:c.634C>T, XM_017015244.3:c.730C>T, XM_017015244.2:c.730C>T, XM_017015244.1:c.730C>T, XM_017015241.3:c.565C>T, XM_017015241.2:c.565C>T, XM_017015241.1:c.913C>T, XM_017015247.3:c.730C>T, XM_017015247.2:c.730C>T, XM_017015247.1:c.730C>T, NM_001077181.3:c.730C>T, NM_001077181.2:c.730C>T, NM_001077181.1:c.730C>T, NM_001351567.3:c.841C>T, NM_001351567.2:c.841C>T, NM_001351567.1:c.841C>T, NM_001351568.3:c.730C>T, NM_001351568.2:c.730C>T, NM_001351568.1:c.730C>T, XR_001746406.3:n.919C>T, XR_001746406.2:n.774C>T, XR_001746406.1:n.1237C>T, NR_147239.2:n.1306C>T, NR_147239.1:n.1293C>T, NM_001351569.2:c.730C>T, NM_001351569.1:c.730C>T, XM_017015245.2:c.823C>T, XM_017015245.1:c.823C>T, XM_047424001.1:c.556C>T, XM_047424003.1:c.556C>T, XM_047424002.1:c.556C>T, XM_047424004.1:c.556C>T, XM_047424000.1:c.634C>T, NM_001351570.1:c.772C>T, NM_033332.1:c.841C>T, XM_047424005.1:c.274C>T, XM_047424006.1:c.43C>T, XR_007061367.1:n.919C>T, XR_007061366.1:n.919C>T, XM_047423999.1:c.841C>T, XM_047423998.1:c.841C>T, XM_047423997.1:c.772C>T, NP_003662.1:p.His281Tyr, XP_011517458.2:p.His275Tyr, NP_201588.1:p.His281Tyr, XP_011517450.2:p.His258Tyr, XP_011517455.2:p.His258Tyr, XP_011517449.2:p.His258Tyr, XP_011517453.2:p.His258Tyr, XP_011517451.2:p.His258Tyr, XP_016870731.1:p.His281Tyr, XP_016870729.2:p.His258Tyr, XP_016870737.1:p.His212Tyr, XP_016870733.1:p.His244Tyr, XP_016870730.2:p.His189Tyr, XP_016870736.1:p.His244Tyr, NP_001070649.1:p.His244Tyr, NP_001338496.1:p.His281Tyr, NP_001338497.1:p.His244Tyr, NP_001338498.1:p.His244Tyr, XP_016870734.1:p.His275Tyr, XP_047279957.1:p.His186Tyr, XP_047279959.1:p.His186Tyr, XP_047279958.1:p.His186Tyr, XP_047279960.1:p.His186Tyr, XP_047279956.1:p.His212Tyr, NP_001338499.1:p.His258Tyr, XP_047279961.1:p.His92Tyr, XP_047279962.1:p.His15Tyr, XP_047279955.1:p.His281Tyr, XP_047279954.1:p.His281Tyr, XP_047279953.1:p.His258Tyr

                                    18.

                                    rs1446218134 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      T>C [Show Flanks]
                                      Chromosome:
                                      9:96534507 (GRCh38)
                                      9:99296789 (GRCh37)
                                      Canonical SPDI:
                                      NC_000009.12:96534506:T:C
                                      Gene:
                                      CDC14B (Varview)
                                      Functional Consequence:
                                      non_coding_transcript_variant,coding_sequence_variant,synonymous_variant,5_prime_UTR_variant
                                      Validated:
                                      by frequency
                                      MAF:
                                      C=0.000004/1 (GnomAD_exomes)
                                      HGVS:
                                      NC_000009.12:g.96534507T>C, NC_000009.11:g.99296789T>C, NM_003671.5:c.663A>G, NM_003671.4:c.663A>G, NM_003671.3:c.663A>G, XM_011519156.4:c.645A>G, XM_011519156.3:c.645A>G, XM_011519156.2:c.645A>G, XM_011519156.1:c.645A>G, NM_033331.4:c.663A>G, NM_033331.3:c.663A>G, NM_033331.2:c.663A>G, XM_011519148.4:c.594A>G, XM_011519148.3:c.594A>G, XM_011519148.2:c.942A>G, XM_011519148.1:c.942A>G, XM_011519153.4:c.594A>G, XM_011519153.3:c.594A>G, XM_011519153.2:c.942A>G, XM_011519153.1:c.942A>G, XR_929864.4:n.741A>G, XR_929864.3:n.596A>G, XR_929864.2:n.1062A>G, XR_929864.1:n.957A>G, XM_011519147.4:c.594A>G, XM_011519147.3:c.594A>G, XM_011519147.2:c.942A>G, XM_011519147.1:c.942A>G, XR_929865.4:n.741A>G, XR_929865.3:n.596A>G, XR_929865.2:n.1062A>G, XR_929865.1:n.957A>G, XM_011519151.4:c.594A>G, XM_011519151.3:c.594A>G, XM_011519151.2:c.942A>G, XM_011519151.1:c.942A>G, XM_011519149.4:c.594A>G, XM_011519149.3:c.594A>G, XM_011519149.2:c.942A>G, XM_011519149.1:c.942A>G, XM_017015242.3:c.663A>G, XM_017015242.2:c.663A>G, XM_017015242.1:c.663A>G, XM_017015240.3:c.594A>G, XM_017015240.2:c.594A>G, XM_017015240.1:c.942A>G, XM_017015248.3:c.456A>G, XM_017015248.2:c.456A>G, XM_017015248.1:c.456A>G, XM_017015244.3:c.552A>G, XM_017015244.2:c.552A>G, XM_017015244.1:c.552A>G, XM_017015241.3:c.387A>G, XM_017015241.2:c.387A>G, XM_017015241.1:c.735A>G, XM_017015247.3:c.552A>G, XM_017015247.2:c.552A>G, XM_017015247.1:c.552A>G, NM_001077181.3:c.552A>G, NM_001077181.2:c.552A>G, NM_001077181.1:c.552A>G, NM_001351567.3:c.663A>G, NM_001351567.2:c.663A>G, NM_001351567.1:c.663A>G, NM_001351568.3:c.552A>G, NM_001351568.2:c.552A>G, NM_001351568.1:c.552A>G, XR_001746406.3:n.741A>G, XR_001746406.2:n.596A>G, XR_001746406.1:n.1059A>G, NR_147239.2:n.1128A>G, NR_147239.1:n.1115A>G, NM_001351569.2:c.552A>G, NM_001351569.1:c.552A>G, XM_017015245.2:c.645A>G, XM_017015245.1:c.645A>G, XM_047424001.1:c.378A>G, XM_047424003.1:c.378A>G, XM_047424002.1:c.378A>G, XM_047424004.1:c.378A>G, XM_047424000.1:c.456A>G, NM_001351570.1:c.594A>G, NM_033332.1:c.663A>G, XM_047424005.1:c.96A>G, XM_047424006.1:c.-136A>G, XR_007061367.1:n.741A>G, XR_007061366.1:n.741A>G, XM_047423999.1:c.663A>G, XM_047423998.1:c.663A>G, XM_047423997.1:c.594A>G

                                      19.

                                      rs1443188011 [Homo sapiens]
                                        Variant type:
                                        DELINS
                                        Alleles:
                                        AGTG>- [Show Flanks]
                                        Chromosome:
                                        9:96564829 (GRCh38)
                                        9:99327111 (GRCh37)
                                        Canonical SPDI:
                                        NC_000009.12:96564826:TGAGTG:TG
                                        Gene:
                                        CDC14B (Varview)
                                        Functional Consequence:
                                        non_coding_transcript_variant,5_prime_UTR_variant,coding_sequence_variant,frameshift_variant,genic_upstream_transcript_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        TG=0./0 (ALFA)
                                        -=0.000004/1 (TOPMED)
                                        -=0.000007/1 (GnomAD)
                                        HGVS:
                                        NC_000009.12:g.96564829_96564832del, NC_000009.11:g.99327111_99327114del, NM_003671.5:c.274_277del, NM_003671.4:c.274_277del, NM_003671.3:c.274_277del, XM_011519156.4:c.256_259del, XM_011519156.3:c.256_259del, XM_011519156.2:c.256_259del, XM_011519156.1:c.256_259del, NM_033331.4:c.274_277del, NM_033331.3:c.274_277del, NM_033331.2:c.274_277del, XM_011519148.4:c.205_208del, XM_011519148.3:c.205_208del, XM_011519148.2:c.553_556del, XM_011519148.1:c.553_556del, XM_011519153.4:c.205_208del, XM_011519153.3:c.205_208del, XM_011519153.2:c.553_556del, XM_011519153.1:c.553_556del, XR_929864.4:n.352_355del, XR_929864.3:n.207_210del, XR_929864.2:n.673_676del, XR_929864.1:n.568_571del, XM_011519147.4:c.205_208del, XM_011519147.3:c.205_208del, XM_011519147.2:c.553_556del, XM_011519147.1:c.553_556del, XR_929865.4:n.352_355del, XR_929865.3:n.207_210del, XR_929865.2:n.673_676del, XR_929865.1:n.568_571del, XM_011519151.4:c.205_208del, XM_011519151.3:c.205_208del, XM_011519151.2:c.553_556del, XM_011519151.1:c.553_556del, XM_011519149.4:c.205_208del, XM_011519149.3:c.205_208del, XM_011519149.2:c.553_556del, XM_011519149.1:c.553_556del, XM_017015242.3:c.274_277del, XM_017015242.2:c.274_277del, XM_017015242.1:c.274_277del, XM_017015240.3:c.205_208del, XM_017015240.2:c.205_208del, XM_017015240.1:c.553_556del, XM_017015248.3:c.274_277del, XM_017015248.2:c.274_277del, XM_017015248.1:c.274_277del, XM_017015244.3:c.163_166del, XM_017015244.2:c.163_166del, XM_017015244.1:c.163_166del, XM_017015241.3:c.205_208del, XM_017015241.2:c.205_208del, XM_017015241.1:c.553_556del, XM_017015247.3:c.163_166del, XM_017015247.2:c.163_166del, XM_017015247.1:c.163_166del, NM_001077181.3:c.163_166del, NM_001077181.2:c.163_166del, NM_001077181.1:c.163_166del, NM_001351567.3:c.274_277del, NM_001351567.2:c.274_277del, NM_001351567.1:c.274_277del, NM_001351568.3:c.163_166del, NM_001351568.2:c.163_166del, NM_001351568.1:c.163_166del, XR_001746406.3:n.352_355del, XR_001746406.2:n.207_210del, XR_001746406.1:n.670_673del, NR_147239.2:n.739_742del, NR_147239.1:n.726_729del, NM_001351569.2:c.163_166del, NM_001351569.1:c.163_166del, XM_017015245.2:c.256_259del, XM_017015245.1:c.256_259del, XM_047424001.1:c.-12_-9del, XM_047424003.1:c.-12_-9del, XM_047424002.1:c.-12_-9del, XM_047424004.1:c.-12_-9del, XM_047424000.1:c.274_277del, NM_001351570.1:c.205_208del, NM_033332.1:c.274_277del, XR_007061367.1:n.352_355del, XR_007061366.1:n.352_355del, XM_047423999.1:c.274_277del, XM_047423998.1:c.274_277del, XM_047423997.1:c.205_208del, NP_003662.1:p.Leu92fs, XP_011517458.2:p.Leu86fs, NP_201588.1:p.Leu92fs, XP_011517450.2:p.Leu69fs, XP_011517455.2:p.Leu69fs, XP_011517449.2:p.Leu69fs, XP_011517453.2:p.Leu69fs, XP_011517451.2:p.Leu69fs, XP_016870731.1:p.Leu92fs, XP_016870729.2:p.Leu69fs, XP_016870737.1:p.Leu92fs, XP_016870733.1:p.Leu55fs, XP_016870730.2:p.Leu69fs, XP_016870736.1:p.Leu55fs, NP_001070649.1:p.Leu55fs, NP_001338496.1:p.Leu92fs, NP_001338497.1:p.Leu55fs, NP_001338498.1:p.Leu55fs, XP_016870734.1:p.Leu86fs, XP_047279956.1:p.Leu92fs, NP_001338499.1:p.Leu69fs, XP_047279955.1:p.Leu92fs, XP_047279954.1:p.Leu92fs, XP_047279953.1:p.Leu69fs

                                        20.

                                        rs1441359507 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          G>A [Show Flanks]
                                          Chromosome:
                                          9:96534059 (GRCh38)
                                          9:99296341 (GRCh37)
                                          Canonical SPDI:
                                          NC_000009.12:96534058:G:A
                                          Gene:
                                          CDC14B (Varview)
                                          Functional Consequence:
                                          non_coding_transcript_variant,missense_variant,coding_sequence_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          A=0./0 (ALFA)
                                          A=0.000004/1 (TOPMED)
                                          A=0.000012/3 (GnomAD_exomes)
                                          A=0.000014/2 (GnomAD)
                                          HGVS:
                                          NC_000009.12:g.96534059G>A, NC_000009.11:g.99296341G>A, NM_003671.5:c.814C>T, NM_003671.4:c.814C>T, NM_003671.3:c.814C>T, XM_011519156.4:c.796C>T, XM_011519156.3:c.796C>T, XM_011519156.2:c.796C>T, XM_011519156.1:c.796C>T, NM_033331.4:c.814C>T, NM_033331.3:c.814C>T, NM_033331.2:c.814C>T, XM_011519148.4:c.745C>T, XM_011519148.3:c.745C>T, XM_011519148.2:c.1093C>T, XM_011519148.1:c.1093C>T, XM_011519153.4:c.745C>T, XM_011519153.3:c.745C>T, XM_011519153.2:c.1093C>T, XM_011519153.1:c.1093C>T, XR_929864.4:n.892C>T, XR_929864.3:n.747C>T, XR_929864.2:n.1213C>T, XR_929864.1:n.1108C>T, XM_011519147.4:c.745C>T, XM_011519147.3:c.745C>T, XM_011519147.2:c.1093C>T, XM_011519147.1:c.1093C>T, XR_929865.4:n.892C>T, XR_929865.3:n.747C>T, XR_929865.2:n.1213C>T, XR_929865.1:n.1108C>T, XM_011519151.4:c.745C>T, XM_011519151.3:c.745C>T, XM_011519151.2:c.1093C>T, XM_011519151.1:c.1093C>T, XM_011519149.4:c.745C>T, XM_011519149.3:c.745C>T, XM_011519149.2:c.1093C>T, XM_011519149.1:c.1093C>T, XM_017015242.3:c.814C>T, XM_017015242.2:c.814C>T, XM_017015242.1:c.814C>T, XM_017015240.3:c.745C>T, XM_017015240.2:c.745C>T, XM_017015240.1:c.1093C>T, XM_017015248.3:c.607C>T, XM_017015248.2:c.607C>T, XM_017015248.1:c.607C>T, XM_017015244.3:c.703C>T, XM_017015244.2:c.703C>T, XM_017015244.1:c.703C>T, XM_017015241.3:c.538C>T, XM_017015241.2:c.538C>T, XM_017015241.1:c.886C>T, XM_017015247.3:c.703C>T, XM_017015247.2:c.703C>T, XM_017015247.1:c.703C>T, NM_001077181.3:c.703C>T, NM_001077181.2:c.703C>T, NM_001077181.1:c.703C>T, NM_001351567.3:c.814C>T, NM_001351567.2:c.814C>T, NM_001351567.1:c.814C>T, NM_001351568.3:c.703C>T, NM_001351568.2:c.703C>T, NM_001351568.1:c.703C>T, XR_001746406.3:n.892C>T, XR_001746406.2:n.747C>T, XR_001746406.1:n.1210C>T, NR_147239.2:n.1279C>T, NR_147239.1:n.1266C>T, NM_001351569.2:c.703C>T, NM_001351569.1:c.703C>T, XM_017015245.2:c.796C>T, XM_017015245.1:c.796C>T, XM_047424001.1:c.529C>T, XM_047424003.1:c.529C>T, XM_047424002.1:c.529C>T, XM_047424004.1:c.529C>T, XM_047424000.1:c.607C>T, NM_001351570.1:c.745C>T, NM_033332.1:c.814C>T, XM_047424005.1:c.247C>T, XM_047424006.1:c.16C>T, XR_007061367.1:n.892C>T, XR_007061366.1:n.892C>T, XM_047423999.1:c.814C>T, XM_047423998.1:c.814C>T, XM_047423997.1:c.745C>T, NP_003662.1:p.Arg272Cys, XP_011517458.2:p.Arg266Cys, NP_201588.1:p.Arg272Cys, XP_011517450.2:p.Arg249Cys, XP_011517455.2:p.Arg249Cys, XP_011517449.2:p.Arg249Cys, XP_011517453.2:p.Arg249Cys, XP_011517451.2:p.Arg249Cys, XP_016870731.1:p.Arg272Cys, XP_016870729.2:p.Arg249Cys, XP_016870737.1:p.Arg203Cys, XP_016870733.1:p.Arg235Cys, XP_016870730.2:p.Arg180Cys, XP_016870736.1:p.Arg235Cys, NP_001070649.1:p.Arg235Cys, NP_001338496.1:p.Arg272Cys, NP_001338497.1:p.Arg235Cys, NP_001338498.1:p.Arg235Cys, XP_016870734.1:p.Arg266Cys, XP_047279957.1:p.Arg177Cys, XP_047279959.1:p.Arg177Cys, XP_047279958.1:p.Arg177Cys, XP_047279960.1:p.Arg177Cys, XP_047279956.1:p.Arg203Cys, NP_001338499.1:p.Arg249Cys, XP_047279961.1:p.Arg83Cys, XP_047279962.1:p.Arg6Cys, XP_047279955.1:p.Arg272Cys, XP_047279954.1:p.Arg272Cys, XP_047279953.1:p.Arg249Cys

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