ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 88
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HGVS dbSNP gnomAD frequency
NM_001369.3(DNAH5):c.1537-50G>A rs150679902 0.01752
NM_001369.3(DNAH5):c.5272-32T>C rs368185722 0.01210
NM_001369.3(DNAH5):c.2052+22C>A rs150480592 0.00621
NM_001369.3(DNAH5):c.9373+38G>A rs116721273 0.00451
NM_001369.3(DNAH5):c.8757G>C (p.Glu2919Asp) rs115776799 0.00334
NM_001369.3(DNAH5):c.5266G>A (p.Glu1756Lys) rs116524991 0.00282
NM_001369.3(DNAH5):c.4510G>C (p.Gly1504Arg) rs143567667 0.00277
NM_001369.3(DNAH5):c.7752+10T>C rs149460805 0.00253
NM_001369.3(DNAH5):c.9681A>G (p.Lys3227=) rs138639741 0.00252
NM_001369.3(DNAH5):c.8805G>C (p.Met2935Ile) rs77874614 0.00250
NM_001369.3(DNAH5):c.12346A>G (p.Ile4116Val) rs34920399 0.00249
NM_001369.3(DNAH5):c.624C>T (p.Asn208=) rs139640247 0.00228
NM_001369.3(DNAH5):c.9355A>G (p.Lys3119Glu) rs76690956 0.00205
NM_001369.3(DNAH5):c.10294G>T (p.Val3432Leu) rs143251588 0.00185
NM_001369.3(DNAH5):c.10323G>A (p.Met3441Ile) rs149133845 0.00185
NM_001369.3(DNAH5):c.3514C>A (p.Gln1172Lys) rs141168110 0.00184
NM_001369.3(DNAH5):c.1356G>A (p.Lys452=) rs144748846 0.00176
NM_001369.3(DNAH5):c.1321-15T>C rs202081804 0.00160
NM_001369.3(DNAH5):c.6039A>C (p.Arg2013=) rs112102932 0.00132
NM_001369.3(DNAH5):c.7065T>C (p.Asp2355=) rs149045168 0.00128
NM_001369.3(DNAH5):c.2443T>A (p.Leu815Met) rs149654950 0.00124
NM_001369.3(DNAH5):c.7753-9C>G rs377367981 0.00122
NM_001369.3(DNAH5):c.3775G>A (p.Ala1259Thr) rs112217391 0.00120
NM_001369.3(DNAH5):c.2355C>T (p.Leu785=) rs112238091 0.00114
NM_001369.3(DNAH5):c.1251C>T (p.Thr417=) rs112911055 0.00109
NM_001369.3(DNAH5):c.1644+12A>G rs201116549 0.00106
NM_001369.3(DNAH5):c.88C>T (p.Arg30Trp) rs114220185 0.00096
NM_001369.3(DNAH5):c.2578-36A>T rs199959119 0.00079
NM_001369.3(DNAH5):c.1645-26C>T rs201631179 0.00073
NM_001369.3(DNAH5):c.4509C>T (p.Thr1503=) rs138157585 0.00070
NM_001369.3(DNAH5):c.8224+15G>A rs148099176 0.00070
NM_001369.3(DNAH5):c.6445-20A>G rs181135242 0.00068
NM_001369.3(DNAH5):c.3777G>A (p.Ala1259=) rs144893234 0.00052
NM_001369.3(DNAH5):c.3534C>T (p.Asn1178=) rs151274810 0.00046
NM_001369.3(DNAH5):c.2067T>C (p.His689=) rs140630779 0.00037
NM_001369.3(DNAH5):c.3843T>C (p.Tyr1281=) rs146492613 0.00037
NM_001369.3(DNAH5):c.11570+8T>C rs369789559 0.00031
NM_001369.3(DNAH5):c.507G>A (p.Ser169=) rs146663590 0.00030
NM_001369.3(DNAH5):c.4054-20T>C rs371107640 0.00029
NM_001369.3(DNAH5):c.8247C>T (p.Tyr2749=) rs367946282 0.00027
NM_001369.3(DNAH5):c.11570+13G>A rs80199741 0.00024
NM_001369.3(DNAH5):c.12279+20T>G rs201220143 0.00024
NM_001369.3(DNAH5):c.11761+5A>G rs780205801 0.00022
NM_001369.3(DNAH5):c.5196G>T (p.Ala1732=) rs201484389 0.00022
NM_001369.3(DNAH5):c.12367C>T (p.His4123Tyr) rs151145750 0.00019
NM_001369.3(DNAH5):c.4687G>A (p.Gly1563Ser) rs147567352 0.00015
NM_001369.3(DNAH5):c.13492-15T>C rs192514899 0.00014
NM_001369.3(DNAH5):c.4258A>G (p.Asn1420Asp) rs201841311 0.00014
NM_001369.3(DNAH5):c.4053+13C>T rs543363871 0.00011
NM_001369.3(DNAH5):c.11211+42T>C rs375467545 0.00007
NM_001369.3(DNAH5):c.10035T>C (p.Cys3345=) rs150268680 0.00006
NM_001369.3(DNAH5):c.2577+5T>C rs201596289 0.00006
NM_001369.3(DNAH5):c.2708A>C (p.Asn903Thr) rs749503841 0.00006
NM_001369.3(DNAH5):c.3396+24C>T rs752204434 0.00006
NM_001369.3(DNAH5):c.573C>T (p.Asp191=) rs773770450 0.00006
NM_001369.3(DNAH5):c.5907T>C (p.Ala1969=) rs569572855 0.00006
NM_001369.3(DNAH5):c.192+19C>T rs374317093 0.00005
NM_001369.3(DNAH5):c.558C>T (p.Leu186=) rs145895917 0.00004
NM_001369.3(DNAH5):c.11571-9A>G rs779715252 0.00003
NM_001369.3(DNAH5):c.11570+4C>T rs771601699 0.00002
NM_001369.3(DNAH5):c.6167A>T (p.Lys2056Ile) rs578128759 0.00002
NM_001369.3(DNAH5):c.7465C>T (p.Leu2489=) rs771511314 0.00002
NM_001369.3(DNAH5):c.10878G>A (p.Thr3626=) rs188428209 0.00001
NM_001369.3(DNAH5):c.11631C>T (p.Tyr3877=) rs776957889 0.00001
NM_001369.3(DNAH5):c.13724-7T>G rs775698729 0.00001
NM_001369.3(DNAH5):c.348C>T (p.Thr116=) rs775947029 0.00001
NM_001369.3(DNAH5):c.3861T>C (p.Tyr1287=) rs764026489 0.00001
NM_001369.3(DNAH5):c.-8C>T rs199528866
NM_001369.3(DNAH5):c.10197A>C (p.Val3399=) rs756720477
NM_001369.3(DNAH5):c.10545A>G (p.Lys3515=) rs727502972
NM_001369.3(DNAH5):c.11034A>G (p.Lys3678=) rs886038477
NM_001369.3(DNAH5):c.12279+48T>A rs755911946
NM_001369.3(DNAH5):c.12279+6G>C rs762179184
NM_001369.3(DNAH5):c.12690C>T (p.Asp4230=) rs531483632
NM_001369.3(DNAH5):c.13569C>A (p.Asp4523Glu) rs151080414
NM_001369.3(DNAH5):c.2229T>G (p.Asp743Glu) rs1445823
NM_001369.3(DNAH5):c.2577+5T>G rs201596289
NM_001369.3(DNAH5):c.2578-10_2578-7del rs71600031
NM_001369.3(DNAH5):c.269C>A (p.Ala90Glu) rs758559495
NM_001369.3(DNAH5):c.3890A>G (p.Asp1297Gly) rs886038478
NM_001369.3(DNAH5):c.4254G>A (p.Leu1418=) rs548183364
NM_001369.3(DNAH5):c.4356-3_4356-2del rs886038479
NM_001369.3(DNAH5):c.5115-14del rs774650371
NM_001369.3(DNAH5):c.7212T>C (p.Asp2404=) rs876657454
NM_001369.3(DNAH5):c.7888-40G>A rs886038480
NM_001369.3(DNAH5):c.7888-6dup rs745582136
NM_001369.3(DNAH5):c.9147T>C (p.Asn3049=) rs886038481
NM_001369.3(DNAH5):c.9374-22C>T rs886038482

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