ClinVar Miner

List of variants in gene DNAH1 reported by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 50
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HGVS dbSNP gnomAD frequency
NM_015512.5(DNAH1):c.4531G>A (p.Val1511Met) rs61734638 0.01825
NM_015512.5(DNAH1):c.6191A>G (p.Asn2064Ser) rs145673040 0.00959
NM_015512.5(DNAH1):c.6676A>G (p.Ile2226Val) rs112505934 0.00533
NM_015512.5(DNAH1):c.2919C>T (p.His973=) rs149114984 0.00455
NM_015512.5(DNAH1):c.2717A>G (p.Asp906Gly) rs61734644 0.00434
NM_015512.5(DNAH1):c.3111G>A (p.Ser1037=) rs77639782 0.00426
NM_015512.5(DNAH1):c.933C>T (p.Asp311=) rs199505182 0.00414
NM_015512.5(DNAH1):c.2204G>A (p.Ser735Asn) rs187636110 0.00334
NM_015512.5(DNAH1):c.5853G>A (p.Val1951=) rs80128076 0.00327
NM_015512.5(DNAH1):c.7375G>A (p.Glu2459Lys) rs201064587 0.00273
NM_015512.5(DNAH1):c.7193G>A (p.Arg2398His) rs201299120 0.00241
NM_015512.5(DNAH1):c.1287G>A (p.Ser429=) rs202217531 0.00221
NM_015512.5(DNAH1):c.4365C>T (p.Ala1455=) rs185313035 0.00218
NM_015512.5(DNAH1):c.10216G>A (p.Val3406Ile) rs201752275 0.00178
NM_015512.5(DNAH1):c.1442G>A (p.Arg481Gln) rs199870577 0.00176
NM_015512.5(DNAH1):c.11481C>T (p.Asn3827=) rs144605025 0.00088
NM_015512.5(DNAH1):c.9814C>T (p.Arg3272Cys) rs200784189 0.00085
NM_015512.5(DNAH1):c.1093G>T (p.Ala365Ser) rs374001771 0.00083
NM_015512.5(DNAH1):c.1590C>T (p.His530=) rs142935638 0.00078
NM_015512.5(DNAH1):c.5964G>A (p.Glu1988=) rs201198770 0.00058
NM_015512.5(DNAH1):c.6610A>G (p.Met2204Val) rs199912441 0.00051
NM_015512.5(DNAH1):c.6558T>G (p.Ala2186=) rs113617561 0.00036
NM_015512.5(DNAH1):c.12315A>G (p.Gln4105=) rs201156071 0.00031
NM_015512.5(DNAH1):c.888G>C (p.Gln296His) rs200450328 0.00031
NM_015512.5(DNAH1):c.9302A>G (p.Lys3101Arg) rs199884450 0.00025
NM_015512.5(DNAH1):c.1263G>T (p.Thr421=) rs111568726 0.00016
NM_015512.5(DNAH1):c.7410C>T (p.His2470=) rs376198165 0.00014
NM_015512.5(DNAH1):c.12017A>C (p.Gln4006Pro) rs369197857 0.00005
NM_015512.5(DNAH1):c.10344C>T (p.Pro3448=) rs200295282 0.00004
NM_015512.5(DNAH1):c.1072C>T (p.Arg358Trp) rs763243743 0.00004
NM_015512.5(DNAH1):c.1881C>T (p.Ser627=) rs193290403 0.00004
NM_015512.5(DNAH1):c.4375A>C (p.Arg1459=) rs376104739 0.00004
NM_015512.5(DNAH1):c.9660C>T (p.Asn3220=) rs183262663 0.00004
NM_015512.5(DNAH1):c.10071A>G (p.Leu3357=) rs554676148 0.00001
NM_015512.5(DNAH1):c.10076G>A (p.Gly3359Asp) rs1437972390 0.00001
NM_015512.5(DNAH1):c.2526+1G>A rs748612396 0.00001
NM_015512.5(DNAH1):c.4188C>G (p.Asp1396Glu) rs376317081 0.00001
NM_015512.5(DNAH1):c.5680G>A (p.Glu1894Lys) rs758777068 0.00001
NM_015512.5(DNAH1):c.6701C>T (p.Thr2234Met) rs780434919 0.00001
NM_015512.5(DNAH1):c.6941G>A (p.Arg2314His) rs759815756 0.00001
NM_015512.5(DNAH1):c.10686A>C (p.Ala3562=)
NM_015512.5(DNAH1):c.10782C>T (p.Leu3594=)
NM_015512.5(DNAH1):c.1182T>C (p.Tyr394=) rs757617865
NM_015512.5(DNAH1):c.12150G>A (p.Lys4050=)
NM_015512.5(DNAH1):c.1790G>T (p.Arg597Leu)
NM_015512.5(DNAH1):c.3570G>A (p.Pro1190=)
NM_015512.5(DNAH1):c.4635T>C (p.Tyr1545=)
NM_015512.5(DNAH1):c.5773G>T (p.Gly1925Trp) rs558171797
NM_015512.5(DNAH1):c.5804C>A (p.Ala1935Asp)
NM_015512.5(DNAH1):c.643T>A (p.Ser215Thr) rs2153223043

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