ClinVar Miner

List of variants in gene DNAH1 reported as likely benign

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Gene type:
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Total variants: 69
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HGVS dbSNP
NM_015512.5(DNAH1):c.10071A>G (p.Leu3357=) rs554676148
NM_015512.5(DNAH1):c.10216G>A (p.Val3406Ile) rs201752275
NM_015512.5(DNAH1):c.10616A>G (p.Lys3539Arg) rs115647631
NM_015512.5(DNAH1):c.10627-10C>T rs1411379067
NM_015512.5(DNAH1):c.10683G>A (p.Pro3561=) rs372328204
NM_015512.5(DNAH1):c.10765G>A (p.Asp3589Asn) rs200850423
NM_015512.5(DNAH1):c.10803C>T (p.Phe3601=) rs373290672
NM_015512.5(DNAH1):c.10852T>C (p.Tyr3618His) rs199603472
NM_015512.5(DNAH1):c.10915G>A (p.Ala3639Thr) rs138940904
NM_015512.5(DNAH1):c.11361C>T (p.Arg3787=) rs372686964
NM_015512.5(DNAH1):c.11481C>T (p.Asn3827=) rs144605025
NM_015512.5(DNAH1):c.11886G>A (p.Thr3962=) rs374930994
NM_015512.5(DNAH1):c.12201_12203CAA[1] (p.Asn4069del) rs772396187
NM_015512.5(DNAH1):c.12261A>G (p.Ser4087=) rs565200964
NM_015512.5(DNAH1):c.12315A>G (p.Gln4105=) rs201156071
NM_015512.5(DNAH1):c.1286+10C>T rs185252204
NM_015512.5(DNAH1):c.1335T>C (p.Tyr445=) rs868394302
NM_015512.5(DNAH1):c.1351A>G (p.Lys451Glu) rs76591348
NM_015512.5(DNAH1):c.1512C>T (p.Leu504=) rs1465711189
NM_015512.5(DNAH1):c.1847A>C (p.Gln616Pro) rs200814267
NM_015512.5(DNAH1):c.1912G>A (p.Asp638Asn) rs201988957
NM_015512.5(DNAH1):c.1955+10G>A rs777008373
NM_015512.5(DNAH1):c.2362C>T (p.Arg788Trp) rs766117149
NM_015512.5(DNAH1):c.2376C>T (p.Ile792=) rs752578416
NM_015512.5(DNAH1):c.269C>T (p.Pro90Leu) rs202174386
NM_015512.5(DNAH1):c.2926G>A (p.Ala976Thr) rs181919231
NM_015512.5(DNAH1):c.3481-9C>T rs774106594
NM_015512.5(DNAH1):c.3573C>T (p.Asp1191=) rs541334137
NM_015512.5(DNAH1):c.4005A>G (p.Glu1335=) rs1553634511
NM_015512.5(DNAH1):c.4575C>T (p.Tyr1525=) rs890356937
NM_015512.5(DNAH1):c.462C>T (p.Ile154=) rs759571672
NM_015512.5(DNAH1):c.4806C>T (p.Thr1602=) rs536663755
NM_015512.5(DNAH1):c.4941G>A (p.Ala1647=) rs369578432
NM_015512.5(DNAH1):c.5100C>G (p.Leu1700=) rs368364427
NM_015512.5(DNAH1):c.5214C>T (p.Phe1738=) rs200175873
NM_015512.5(DNAH1):c.5332-14G>A rs375828810
NM_015512.5(DNAH1):c.5396A>G (p.Lys1799Arg) rs200793269
NM_015512.5(DNAH1):c.5772C>T (p.Asp1924=) rs187752630
NM_015512.5(DNAH1):c.5850G>A (p.Pro1950=) rs374690567
NM_015512.5(DNAH1):c.5964G>A (p.Glu1988=) rs201198770
NM_015512.5(DNAH1):c.6120C>G (p.Leu2040=) rs1295311826
NM_015512.5(DNAH1):c.6180C>T (p.Ile2060=) rs369225035
NM_015512.5(DNAH1):c.6418-6C>T rs201832370
NM_015512.5(DNAH1):c.6460A>G (p.Arg2154Gly) rs146002323
NM_015512.5(DNAH1):c.6558T>G (p.Ala2186=) rs113617561
NM_015512.5(DNAH1):c.6676A>G (p.Ile2226Val) rs112505934
NM_015512.5(DNAH1):c.678G>A (p.Gln226=) rs1553627030
NM_015512.5(DNAH1):c.7109A>C (p.Asp2370Ala) rs202011102
NM_015512.5(DNAH1):c.7161T>C (p.Asp2387=) rs746450942
NM_015512.5(DNAH1):c.7193G>A (p.Arg2398His) rs201299120
NM_015512.5(DNAH1):c.7263A>G (p.Ala2421=) rs375105856
NM_015512.5(DNAH1):c.732A>G (p.Pro244=) rs374941590
NM_015512.5(DNAH1):c.7410C>T (p.His2470=) rs376198165
NM_015512.5(DNAH1):c.7805+6C>T rs370368596
NM_015512.5(DNAH1):c.7809C>T (p.Ala2603=) rs368368003
NM_015512.5(DNAH1):c.7923C>T (p.Phe2641=) rs372331607
NM_015512.5(DNAH1):c.7941+7C>T rs1445414596
NM_015512.5(DNAH1):c.8448C>T (p.Ile2816=) rs769821553
NM_015512.5(DNAH1):c.8514+10G>C rs545437483
NM_015512.5(DNAH1):c.8625+7del rs1196963237
NM_015512.5(DNAH1):c.8649G>C (p.Glu2883Asp) rs79689614
NM_015512.5(DNAH1):c.871+3G>A rs200262632
NM_015512.5(DNAH1):c.8885A>C (p.Lys2962Thr) rs199602894
NM_015512.5(DNAH1):c.888G>C (p.Gln296His) rs200450328
NM_015512.5(DNAH1):c.9021G>T (p.Val3007=) rs201550077
NM_015512.5(DNAH1):c.9123C>T (p.Arg3041=) rs368440271
NM_015512.5(DNAH1):c.9343C>T (p.Arg3115Trp) rs185397176
NM_015512.5(DNAH1):c.9364-6C>T rs1553641484
NM_015512.5(DNAH1):c.9440T>A (p.Ile3147Asn) rs61734629

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