ClinVar Miner

List of variants in gene CDC14A reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 59
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HGVS dbSNP gnomAD frequency
NM_003672.4(CDC14A):c.-47T>C rs594529 0.98301
NM_003672.4(CDC14A):c.1251-139A>G rs2270692 0.93245
NM_003672.4(CDC14A):c.1756-184G>A rs3767839 0.90404
NM_003672.4(CDC14A):c.*256T>C rs10783134 0.85569
NM_003672.4(CDC14A):c.839-124T>C rs560431 0.83947
NM_003672.4(CDC14A):c.-225A>T rs527644 0.83113
NM_003672.4(CDC14A):c.457-166A>G rs584350 0.69648
NM_003672.4(CDC14A):c.310-9450A>T rs612683 0.37598
NM_003672.4(CDC14A):c.-333G>C rs529224 0.34303
NM_003672.4(CDC14A):c.607+142A>G rs17122554 0.28479
NM_003672.4(CDC14A):c.50-45T>C rs2297170 0.19987
NM_003672.4(CDC14A):c.519+25A>T rs78861171 0.14018
NM_003672.4(CDC14A):c.309+99C>T rs28361213 0.12381
NM_003672.4(CDC14A):c.990G>A (p.Ser330=) rs2270694 0.11151
NM_003672.4(CDC14A):c.309A>C (p.Ala103=) rs28361212 0.09875
NM_003672.4(CDC14A):c.1299-265T>C rs58882984 0.08907
NM_003672.4(CDC14A):c.977+22C>T rs17122599 0.06177
NM_003672.4(CDC14A):c.838+269C>T rs7543497 0.06152
NM_003672.4(CDC14A):c.825C>T (p.Ala275=) rs7543221 0.06126
NM_003672.4(CDC14A):c.903T>C (p.His301=) rs17122597 0.05859
NM_003672.4(CDC14A):c.838+158C>T rs28364886 0.04512
NM_003672.4(CDC14A):c.519+126G>T rs78315260 0.03834
NM_003672.4(CDC14A):c.519+174A>G rs6687508 0.03441
NM_003672.4(CDC14A):c.608-152G>T rs28364883 0.02664
NM_003672.4(CDC14A):c.519+82T>C rs10493926 0.02148
NM_003672.4(CDC14A):c.310-18A>G rs17122450 0.02143
NM_003672.4(CDC14A):c.217-263T>A rs17122369 0.01660
NM_003672.4(CDC14A):c.141-229G>T rs28361203 0.01657
NM_003672.4(CDC14A):c.1647C>T (p.Ser549=) rs35385659 0.01241
NM_003672.4(CDC14A):c.520-16T>C rs28364872 0.00928
NM_003672.4(CDC14A):c.608-10G>A rs114626664 0.00462
NM_003672.4(CDC14A):c.1755+8C>T rs139956023 0.00461
NM_003672.4(CDC14A):c.819C>G (p.Ala273=) rs28364884 0.00453
NM_003672.4(CDC14A):c.1604A>G (p.Gln535Arg) rs113885721 0.00292
NM_003672.4(CDC14A):c.778G>A (p.Val260Met) rs61755295 0.00239
NM_003672.4(CDC14A):c.1711G>A (p.Gly571Arg) rs61752469 0.00224
NM_003672.4(CDC14A):c.822C>T (p.Ile274=) rs74667145 0.00158
NM_003672.4(CDC14A):c.1034G>A (p.Arg345Gln) rs28364897 0.00102
NM_003672.4(CDC14A):c.1090A>G (p.Ile364Val) rs140849467 0.00065
NM_003672.4(CDC14A):c.309+145A>G rs188427266 0.00057
NM_003672.4(CDC14A):c.957C>T (p.Pro319=) rs554166560 0.00049
NM_003672.4(CDC14A):c.1755+110C>G rs188557928 0.00016
NM_003672.4(CDC14A):c.471A>C (p.Gly157=) rs138318034 0.00005
NM_003672.4(CDC14A):c.717C>T (p.Asp239=) rs765677912 0.00005
NM_003672.4(CDC14A):c.1137+188del rs373460421
NM_003672.4(CDC14A):c.1138-333G>T rs74104803
NM_003672.4(CDC14A):c.1251-4G>A
NM_003672.4(CDC14A):c.1298+188_1298+189del rs149672640
NM_003672.4(CDC14A):c.1298+268dup rs112236843
NM_003672.4(CDC14A):c.1299-159_1299-158del rs35904273
NM_003672.4(CDC14A):c.1299-223T>G rs904296
NM_003672.4(CDC14A):c.309+267A>T rs28361214
NM_003672.4(CDC14A):c.456+15C>G rs28361230
NM_003672.4(CDC14A):c.456+15C>T rs28361230
NM_003672.4(CDC14A):c.519+22dup
NM_003672.4(CDC14A):c.607+14dup rs769091089
NM_003672.4(CDC14A):c.726C>T (p.Phe242=)
NM_003672.4(CDC14A):c.977+25C>A rs147859939
NM_003672.4(CDC14A):c.977+62C>A rs17122602

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