ClinVar Miner

List of variants in gene DNAH5 reported as likely benign for not specified

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Gene type:
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Total variants: 88
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HGVS dbSNP
NM_001369.2(DNAH5):c.-8C>T rs199528866
NM_001369.2(DNAH5):c.10035T>C (p.Cys3345=) rs150268680
NM_001369.2(DNAH5):c.10197A>C (p.Val3399=) rs756720477
NM_001369.2(DNAH5):c.10294G>T (p.Val3432Leu) rs143251588
NM_001369.2(DNAH5):c.10323G>A (p.Met3441Ile) rs149133845
NM_001369.2(DNAH5):c.10545A>G (p.Lys3515=) rs727502972
NM_001369.2(DNAH5):c.10878G>A (p.Thr3626=) rs188428209
NM_001369.2(DNAH5):c.11034A>G (p.Lys3678=) rs886038477
NM_001369.2(DNAH5):c.11211+42T>C rs375467545
NM_001369.2(DNAH5):c.11570+13G>A rs80199741
NM_001369.2(DNAH5):c.11570+4C>T rs771601699
NM_001369.2(DNAH5):c.11570+8T>C rs369789559
NM_001369.2(DNAH5):c.11571-9A>G rs779715252
NM_001369.2(DNAH5):c.11631C>T (p.Tyr3877=) rs776957889
NM_001369.2(DNAH5):c.11761+5A>G rs780205801
NM_001369.2(DNAH5):c.12279+20T>G rs201220143
NM_001369.2(DNAH5):c.12279+48T>A rs755911946
NM_001369.2(DNAH5):c.12279+6G>C rs762179184
NM_001369.2(DNAH5):c.12346A>G (p.Ile4116Val) rs34920399
NM_001369.2(DNAH5):c.12367C>T (p.His4123Tyr) rs151145750
NM_001369.2(DNAH5):c.1251C>T (p.Thr417=) rs112911055
NM_001369.2(DNAH5):c.12690C>T (p.Asp4230=) rs531483632
NM_001369.2(DNAH5):c.1321-15T>C rs202081804
NM_001369.2(DNAH5):c.13492-15T>C rs192514899
NM_001369.2(DNAH5):c.13569C>A (p.Asp4523Glu) rs151080414
NM_001369.2(DNAH5):c.1356G>A (p.Lys452=) rs144748846
NM_001369.2(DNAH5):c.13724-7T>G rs775698729
NM_001369.2(DNAH5):c.1537-50G>A rs150679902
NM_001369.2(DNAH5):c.1644+12A>G rs201116549
NM_001369.2(DNAH5):c.1645-26C>T rs201631179
NM_001369.2(DNAH5):c.192+19C>T rs374317093
NM_001369.2(DNAH5):c.2052+22C>A rs150480592
NM_001369.2(DNAH5):c.2067T>C (p.His689=) rs140630779
NM_001369.2(DNAH5):c.2229T>G (p.Asp743Glu) rs1445823
NM_001369.2(DNAH5):c.2355C>T (p.Leu785=) rs112238091
NM_001369.2(DNAH5):c.2443T>A (p.Leu815Met) rs149654950
NM_001369.2(DNAH5):c.2577+5T>C rs201596289
NM_001369.2(DNAH5):c.2577+5T>G rs201596289
NM_001369.2(DNAH5):c.2578-10_2578-7del rs71600031
NM_001369.2(DNAH5):c.2578-36A>T rs199959119
NM_001369.2(DNAH5):c.269C>A (p.Ala90Glu) rs758559495
NM_001369.2(DNAH5):c.2708A>C (p.Asn903Thr) rs749503841
NM_001369.2(DNAH5):c.3396+24C>T rs752204434
NM_001369.2(DNAH5):c.348C>T (p.Thr116=) rs775947029
NM_001369.2(DNAH5):c.3514C>A (p.Gln1172Lys) rs141168110
NM_001369.2(DNAH5):c.3534C>T (p.Asn1178=) rs151274810
NM_001369.2(DNAH5):c.3775G>A (p.Ala1259Thr) rs112217391
NM_001369.2(DNAH5):c.3777G>A (p.Ala1259=) rs144893234
NM_001369.2(DNAH5):c.3843T>C (p.Tyr1281=) rs146492613
NM_001369.2(DNAH5):c.3861T>C (p.Tyr1287=) rs764026489
NM_001369.2(DNAH5):c.3890A>G (p.Asp1297Gly) rs886038478
NM_001369.2(DNAH5):c.4053+13C>T rs543363871
NM_001369.2(DNAH5):c.4054-20T>C rs371107640
NM_001369.2(DNAH5):c.4254G>A (p.Leu1418=) rs548183364
NM_001369.2(DNAH5):c.4258A>G (p.Asn1420Asp) rs201841311
NM_001369.2(DNAH5):c.4356-3_4356-2delCA rs886038479
NM_001369.2(DNAH5):c.4509C>T (p.Thr1503=) rs138157585
NM_001369.2(DNAH5):c.4510G>C (p.Gly1504Arg) rs143567667
NM_001369.2(DNAH5):c.4687G>A (p.Gly1563Ser) rs147567352
NM_001369.2(DNAH5):c.507G>A (p.Ser169=) rs146663590
NM_001369.2(DNAH5):c.5115-14delT rs774650371
NM_001369.2(DNAH5):c.5196G>T (p.Ala1732=) rs201484389
NM_001369.2(DNAH5):c.5266G>A (p.Glu1756Lys) rs116524991
NM_001369.2(DNAH5):c.5272-32T>C rs368185722
NM_001369.2(DNAH5):c.558C>T (p.Leu186=) rs145895917
NM_001369.2(DNAH5):c.573C>T (p.Asp191=) rs773770450
NM_001369.2(DNAH5):c.5907T>C (p.Ala1969=) rs569572855
NM_001369.2(DNAH5):c.6039A>C (p.Arg2013=) rs112102932
NM_001369.2(DNAH5):c.6167A>T (p.Lys2056Ile) rs578128759
NM_001369.2(DNAH5):c.624C>T (p.Asn208=) rs139640247
NM_001369.2(DNAH5):c.6445-20A>G rs181135242
NM_001369.2(DNAH5):c.7065T>C (p.Asp2355=) rs149045168
NM_001369.2(DNAH5):c.7212T>C (p.Asp2404=) rs876657454
NM_001369.2(DNAH5):c.7465C>T (p.Leu2489=) rs771511314
NM_001369.2(DNAH5):c.7752+10T>C rs149460805
NM_001369.2(DNAH5):c.7753-9C>G rs377367981
NM_001369.2(DNAH5):c.7888-40G>A rs886038480
NM_001369.2(DNAH5):c.7888-6dupT rs745582136
NM_001369.2(DNAH5):c.8224+15G>A rs148099176
NM_001369.2(DNAH5):c.8247C>T (p.Tyr2749=) rs367946282
NM_001369.2(DNAH5):c.8757G>C (p.Glu2919Asp) rs115776799
NM_001369.2(DNAH5):c.8805G>C (p.Met2935Ile) rs77874614
NM_001369.2(DNAH5):c.88C>T (p.Arg30Trp) rs114220185
NM_001369.2(DNAH5):c.9147T>C (p.Asn3049=) rs886038481
NM_001369.2(DNAH5):c.9355A>G (p.Lys3119Glu) rs76690956
NM_001369.2(DNAH5):c.9373+38G>A rs116721273
NM_001369.2(DNAH5):c.9374-22C>T rs886038482
NM_001369.2(DNAH5):c.9681A>G (p.Lys3227=) rs138639741

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