ClinVar Miner

List of variants in gene CDC14A reported as uncertain significance for not provided

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Total variants: 60
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HGVS dbSNP gnomAD frequency
NM_003672.4(CDC14A):c.31G>A (p.Ala11Thr) rs140623300 0.00054
NM_003672.4(CDC14A):c.476T>A (p.Phe159Tyr) rs568592855 0.00016
NM_003672.4(CDC14A):c.512A>T (p.His171Leu) rs780275633 0.00016
NM_003672.4(CDC14A):c.1081G>A (p.Asp361Asn) rs761856090 0.00008
NM_003672.4(CDC14A):c.1745G>A (p.Arg582His) rs148639495 0.00006
NM_003672.4(CDC14A):c.1744C>T (p.Arg582Cys) rs775050058 0.00003
NM_003672.4(CDC14A):c.456G>A (p.Lys152=) rs774957073 0.00003
NM_003672.4(CDC14A):c.586C>T (p.Pro196Ser) rs755291422 0.00002
NM_003672.4(CDC14A):c.1198C>T (p.Arg400Cys) rs1326031095 0.00001
NM_003672.4(CDC14A):c.1245A>T (p.Ala415=) rs771516972 0.00001
NM_003672.4(CDC14A):c.1268G>A (p.Gly423Glu) rs776723170 0.00001
NM_003672.4(CDC14A):c.542A>G (p.Asn181Ser) rs750581079 0.00001
NM_003672.4(CDC14A):c.632C>G (p.Ala211Gly) rs373986788 0.00001
NM_003672.4(CDC14A):c.706C>T (p.Arg236Cys) rs1482824856 0.00001
NM_003672.4(CDC14A):c.98A>G (p.Asn33Ser) rs796559022 0.00001
NC_000001.10:g.(?_100963621)_(100964935_?)del
NM_003672.4(CDC14A):c.1016G>A (p.Arg339Gln)
NM_003672.4(CDC14A):c.1031A>G (p.Asn344Ser)
NM_003672.4(CDC14A):c.1055T>C (p.Ile352Thr)
NM_003672.4(CDC14A):c.1137+2T>C
NM_003672.4(CDC14A):c.1157A>T (p.Asp386Val)
NM_003672.4(CDC14A):c.1226G>T (p.Arg409Leu) rs375533263
NM_003672.4(CDC14A):c.1299-2del
NM_003672.4(CDC14A):c.12G>T (p.Glu4Asp)
NM_003672.4(CDC14A):c.1371_1386del (p.Ala458fs)
NM_003672.4(CDC14A):c.1381A>T (p.Ile461Phe)
NM_003672.4(CDC14A):c.1436C>A (p.Ser479Tyr)
NM_003672.4(CDC14A):c.1439G>A (p.Arg480Gln)
NM_003672.4(CDC14A):c.1446C>T (p.Ala482=) rs2101441568
NM_003672.4(CDC14A):c.1533C>A (p.Ser511Arg) rs749753871
NM_003672.4(CDC14A):c.161C>T (p.Pro54Leu)
NM_003672.4(CDC14A):c.1640T>G (p.Leu547Arg)
NM_003672.4(CDC14A):c.1655G>T (p.Gly552Val)
NM_003672.4(CDC14A):c.1724del (p.Ser575fs)
NM_003672.4(CDC14A):c.1755+108del rs2101444854
NM_003672.4(CDC14A):c.1755+78_1755+79delinsTT rs2101444645
NM_003672.4(CDC14A):c.1773T>A (p.Tyr591Ter)
NM_003672.4(CDC14A):c.214A>G (p.Lys72Glu) rs2100948826
NM_003672.4(CDC14A):c.251A>G (p.Tyr84Cys) rs143209870
NM_003672.4(CDC14A):c.298G>T (p.Gly100Cys)
NM_003672.4(CDC14A):c.310-12T>C
NM_003672.4(CDC14A):c.346A>G (p.Arg116Gly)
NM_003672.4(CDC14A):c.349G>A (p.Ala117Thr)
NM_003672.4(CDC14A):c.35G>A (p.Cys12Tyr)
NM_003672.4(CDC14A):c.370C>G (p.Pro124Ala)
NM_003672.4(CDC14A):c.374C>A (p.Pro125His)
NM_003672.4(CDC14A):c.374C>T (p.Pro125Leu)
NM_003672.4(CDC14A):c.43A>G (p.Met15Val)
NM_003672.4(CDC14A):c.547_552del (p.Ile183_Val184del)
NM_003672.4(CDC14A):c.613C>T (p.Pro205Ser)
NM_003672.4(CDC14A):c.632C>T (p.Ala211Val)
NM_003672.4(CDC14A):c.694del (p.Tyr232fs) rs1309255666
NM_003672.4(CDC14A):c.707G>T (p.Arg236Leu)
NM_003672.4(CDC14A):c.782G>A (p.Arg261Gln)
NM_003672.4(CDC14A):c.811G>A (p.Glu271Lys)
NM_003672.4(CDC14A):c.848G>C (p.Gly283Ala)
NM_003672.4(CDC14A):c.877G>A (p.Val293Ile)
NM_003672.4(CDC14A):c.913A>G (p.Ile305Val)
NM_003672.4(CDC14A):c.935G>C (p.Arg312Pro)
NM_003672.4(CDC14A):c.998T>C (p.Val333Ala)

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