ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 81
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HGVS dbSNP gnomAD frequency
NM_003672.4(CDC14A):c.607+30C>A rs28364873 0.01372
NM_003672.4(CDC14A):c.390-142G>A rs28361228 0.01297
NM_003672.4(CDC14A):c.141-293T>C rs28361201 0.01233
NM_003672.4(CDC14A):c.520-16T>C rs28364872 0.00928
NM_003672.4(CDC14A):c.520-60C>T rs28364871 0.00861
NM_001319211.2(CDC14A):c.-125-1564C>G rs549887762 0.00629
NM_001319211.2(CDC14A):c.-125-1565G>A rs529737374 0.00628
NM_003672.4(CDC14A):c.607+182A>T rs114112363 0.00620
NM_003672.4(CDC14A):c.838+75C>G rs6690073 0.00554
NM_003672.3(CDC14A):c.-470A>G rs542747022 0.00539
NM_003672.4(CDC14A):c.839-108T>C rs115808928 0.00473
NM_003672.4(CDC14A):c.819C>G (p.Ala273=) rs28364884 0.00453
NM_003672.4(CDC14A):c.456+111A>G rs76679045 0.00451
NM_003672.4(CDC14A):c.140+281C>G rs149981742 0.00424
NM_003672.4(CDC14A):c.456+208G>A rs601077 0.00404
NM_003672.4(CDC14A):c.390-83C>T rs28361229 0.00378
NM_003672.4(CDC14A):c.1299-201C>A rs187487999 0.00320
NM_003672.4(CDC14A):c.1604A>G (p.Gln535Arg) rs113885721 0.00292
NM_003672.4(CDC14A):c.1730C>T (p.Ala577Val) rs112231082 0.00118
NM_003672.4(CDC14A):c.192C>T (p.Cys64=) rs201731089 0.00118
NM_003672.4(CDC14A):c.1034G>A (p.Arg345Gln) rs28364897 0.00102
NM_003672.4(CDC14A):c.457-6T>C rs202211124 0.00093
NM_003672.4(CDC14A):c.1090A>G (p.Ile364Val) rs140849467 0.00065
NM_003672.4(CDC14A):c.31G>A (p.Ala11Thr) rs140623300 0.00054
NM_003672.4(CDC14A):c.1755+72G>A rs139348402 0.00051
NM_003672.4(CDC14A):c.957C>T (p.Pro319=) rs554166560 0.00049
NM_003672.4(CDC14A):c.1071T>C (p.Ser357=) rs111580443 0.00012
NM_003672.4(CDC14A):c.1251-5C>T rs375381230 0.00011
NM_003672.4(CDC14A):c.1535C>T (p.Pro512Leu) rs143117380 0.00011
NM_003672.4(CDC14A):c.1298+16T>C rs186169849 0.00009
NM_003672.4(CDC14A):c.748A>G (p.Ile250Val) rs200624804 0.00009
NM_003672.4(CDC14A):c.717C>T (p.Asp239=) rs765677912 0.00005
NM_003672.4(CDC14A):c.1421+12C>T rs533462367 0.00004
NM_003672.4(CDC14A):c.1701C>G (p.Pro567=) rs779179736 0.00004
NM_003672.4(CDC14A):c.1217G>A (p.Arg406Lys) rs748922639 0.00003
NM_003672.4(CDC14A):c.1665C>T (p.Ser555=) rs370790422 0.00003
NM_003672.4(CDC14A):c.1033C>A (p.Arg345=) rs549556142 0.00001
NM_003672.4(CDC14A):c.1245A>T (p.Ala415=) rs771516972 0.00001
NM_003672.4(CDC14A):c.1371G>A (p.Thr457=) rs751290983 0.00001
NM_003672.4(CDC14A):c.780G>A (p.Val260=) rs760951536 0.00001
NM_003672.4(CDC14A):c.966C>T (p.His322=) rs574121540 0.00001
NM_001319211.2(CDC14A):c.-125-1978A>G
NM_003672.4(CDC14A):c.1128A>T (p.Arg376=)
NM_003672.4(CDC14A):c.1138-17C>T
NM_003672.4(CDC14A):c.1158T>C (p.Asp386=) rs1571338835
NM_003672.4(CDC14A):c.1263A>T (p.Thr421=)
NM_003672.4(CDC14A):c.1298+187_1298+189del rs149672640
NM_003672.4(CDC14A):c.1298+189del rs149672640
NM_003672.4(CDC14A):c.1299-6G>T
NM_003672.4(CDC14A):c.140+9_140+14dup
NM_003672.4(CDC14A):c.1680G>A (p.Glu560=)
NM_003672.4(CDC14A):c.1710C>T (p.Thr570=)
NM_003672.4(CDC14A):c.1755+120G>A
NM_003672.4(CDC14A):c.1755+151A>C rs571214442
NM_003672.4(CDC14A):c.1755+24T>C
NM_003672.4(CDC14A):c.210A>G (p.Lys70=)
NM_003672.4(CDC14A):c.216+7A>G
NM_003672.4(CDC14A):c.217-20T>A
NM_003672.4(CDC14A):c.217-7T>C
NM_003672.4(CDC14A):c.28G>C (p.Gly10Arg) rs571098288
NM_003672.4(CDC14A):c.302C>G (p.Ala101Gly)
NM_003672.4(CDC14A):c.309+19A>T
NM_003672.4(CDC14A):c.309+9del
NM_003672.4(CDC14A):c.357G>C (p.Leu119=)
NM_003672.4(CDC14A):c.432C>T (p.Leu144=)
NM_003672.4(CDC14A):c.456+15C>T rs28361230
NM_003672.4(CDC14A):c.489A>G (p.Thr163=)
NM_003672.4(CDC14A):c.50-11T>G
NM_003672.4(CDC14A):c.520-8dup
NM_003672.4(CDC14A):c.608-7C>A
NM_003672.4(CDC14A):c.60T>C (p.Tyr20=) rs2100872783
NM_003672.4(CDC14A):c.792G>C (p.Leu264=)
NM_003672.4(CDC14A):c.798C>T (p.Ile266=)
NM_003672.4(CDC14A):c.810C>T (p.Thr270=)
NM_003672.4(CDC14A):c.838+17G>A
NM_003672.4(CDC14A):c.838+20G>A
NM_003672.4(CDC14A):c.839-4A>G
NM_003672.4(CDC14A):c.93A>G (p.Thr31=)
NM_003672.4(CDC14A):c.977+15C>T
NM_003672.4(CDC14A):c.977+285del rs147976512
NM_003672.4(CDC14A):c.978-169T>A rs2270693

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