ClinVar Miner

List of variants in gene DNAH1 reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 108
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HGVS dbSNP gnomAD frequency
NM_015512.5(DNAH1):c.7199-157C>T rs71297396 0.03994
NM_015512.5(DNAH1):c.7608+122G>A rs13091360 0.03927
NM_015512.5(DNAH1):c.11959-15C>T rs123603 0.03923
NM_015512.5(DNAH1):c.8515-62C>G rs34827613 0.03855
NM_015512.5(DNAH1):c.11230C>T (p.Arg3744Cys) rs419752 0.03813
NM_015512.5(DNAH1):c.1321G>C (p.Val441Leu) rs13060192 0.03637
NM_015512.5(DNAH1):c.7378-251C>T rs13089892 0.03607
NM_015512.5(DNAH1):c.582-104G>A rs34181173 0.03488
NM_015512.5(DNAH1):c.3853C>T (p.Arg1285Trp) rs61734640 0.03447
NM_015512.5(DNAH1):c.2430C>T (p.Thr810=) rs35982798 0.03445
NM_015512.5(DNAH1):c.4407+70C>T rs71297394 0.03444
NM_015512.5(DNAH1):c.10317C>T (p.Ile3439=) rs419050 0.03434
NM_015512.5(DNAH1):c.1033+229G>A rs139934976 0.02005
NM_015512.5(DNAH1):c.12677-246G>T rs73072980 0.01842
NM_015512.5(DNAH1):c.4531G>A (p.Val1511Met) rs61734638 0.01825
NM_015512.5(DNAH1):c.7569C>T (p.Ser2523=) rs73072968 0.01641
NM_015512.5(DNAH1):c.2646+53G>A rs146121533 0.01326
NM_015512.5(DNAH1):c.11259+279dup rs1553642893 0.01262
NM_015512.5(DNAH1):c.5766-86C>G rs149655599 0.01141
NM_015512.5(DNAH1):c.-34-299G>A rs74762885 0.01104
NM_015512.5(DNAH1):c.4588A>G (p.Asn1530Asp) rs74498533 0.00903
NM_015512.5(DNAH1):c.8215A>G (p.Ile2739Val) rs61734631 0.00845
NM_015512.5(DNAH1):c.10823+50T>C rs146126832 0.00671
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.5765+12C>G rs201223427 0.00360
NM_015512.5(DNAH1):c.3090G>A (p.Ala1030=) rs140275399 0.00355
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.569T>C (p.Ile190Thr) rs61729450 0.00319
NM_015512.5(DNAH1):c.11136G>A (p.Arg3712=) rs147264705 0.00317
NM_015512.5(DNAH1):c.1244A>G (p.Lys415Arg) rs61729402 0.00315
NM_015512.5(DNAH1):c.872-15C>T rs143657729 0.00315
NM_015512.5(DNAH1):c.11788-14C>T rs141567808 0.00310
NM_015512.5(DNAH1):c.12375A>T (p.Thr4125=) rs61734637 0.00310
NM_015512.5(DNAH1):c.8266G>A (p.Val2756Met) rs61749019 0.00304
NM_015512.5(DNAH1):c.10422T>C (p.Leu3474=) rs148913561 0.00302
NM_015512.5(DNAH1):c.11128-24T>C rs186185022 0.00302
NM_015512.5(DNAH1):c.1981A>G (p.Met661Val) rs61734653 0.00302
NM_015512.5(DNAH1):c.2744A>G (p.Asn915Ser) rs61734643 0.00302
NM_015512.5(DNAH1):c.4263C>T (p.Pro1421=) rs61739897 0.00300
NM_015512.5(DNAH1):c.1286+16G>A rs190176840 0.00289
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.5669G>T (p.Gly1890Val) rs200859252 0.00190
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.9343C>T (p.Arg3115Trp) rs185397176 0.00109
NM_015512.5(DNAH1):c.1351A>G (p.Lys451Glu) rs76591348 0.00103
NM_015512.5(DNAH1):c.11481C>T (p.Asn3827=) rs144605025 0.00088
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.7794C>T (p.Leu2598=) rs373044616 0.00021
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.10344C>T (p.Pro3448=) rs200295282 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.11259+9C>T rs774513441 0.00003
NM_015512.5(DNAH1):c.5766-7G>A rs767863684 0.00003
NM_015512.5(DNAH1):c.7371G>A (p.Lys2457=) rs1487753085 0.00003
NM_015512.5(DNAH1):c.8370C>T (p.Ile2790=) rs555969561 0.00003
NM_015512.5(DNAH1):c.4704C>T (p.Thr1568=) rs768564169 0.00002
NM_015512.5(DNAH1):c.10071A>G (p.Leu3357=) rs554676148 0.00001
NM_015512.5(DNAH1):c.10386C>T (p.Asp3462=) rs371037989 0.00001
NM_015512.5(DNAH1):c.11493C>T (p.Arg3831=) rs781581930 0.00001
NM_015512.5(DNAH1):c.1795C>T (p.Leu599=) rs376457125 0.00001
NM_015512.5(DNAH1):c.5943+10C>T rs765825721 0.00001
NM_015512.5(DNAH1):c.6795C>T (p.Thr2265=) rs367699532 0.00001
NM_015512.5(DNAH1):c.10020A>G (p.Lys3340=) rs1578199216
NM_015512.5(DNAH1):c.10065C>T (p.Asp3355=) rs1578200377
NM_015512.5(DNAH1):c.10278+9C>T rs1313257372
NM_015512.5(DNAH1):c.10401C>T (p.Asp3467=) rs1578201431
NM_015512.5(DNAH1):c.10686A>C (p.Ala3562=)
NM_015512.5(DNAH1):c.10782C>T (p.Leu3594=)
NM_015512.5(DNAH1):c.1086C>G (p.Leu362=) rs1299689149
NM_015512.5(DNAH1):c.11661T>C (p.Asp3887=) rs1578208089
NM_015512.5(DNAH1):c.11778C>T (p.Tyr3926=) rs1214030380
NM_015512.5(DNAH1):c.1182T>C (p.Tyr394=) rs757617865
NM_015512.5(DNAH1):c.12150G>A (p.Lys4050=)
NM_015512.5(DNAH1):c.12380C>G (p.Thr4127Ser) rs548795920
NM_015512.5(DNAH1):c.1392C>T (p.Thr464=) rs1578107422
NM_015512.5(DNAH1):c.2241C>T (p.Tyr747=) rs145912972
NM_015512.5(DNAH1):c.3312T>C (p.Pro1104=) rs1445862576
NM_015512.5(DNAH1):c.3570G>A (p.Pro1190=)
NM_015512.5(DNAH1):c.3651G>A (p.Glu1217=) rs1578130186
NM_015512.5(DNAH1):c.4266+8G>A rs533258607
NM_015512.5(DNAH1):c.4635T>C (p.Tyr1545=)
NM_015512.5(DNAH1):c.5611-7C>T rs1578150950
NM_015512.5(DNAH1):c.6309C>T (p.Ile2103=)
NM_015512.5(DNAH1):c.6526-10_6526-9del rs562893788
NM_015512.5(DNAH1):c.7293A>G (p.Pro2431=) rs1359069867
NM_015512.5(DNAH1):c.7563A>G (p.Pro2521=) rs938156099
NM_015512.5(DNAH1):c.7942-49T>G rs150888531
NM_015512.5(DNAH1):c.804A>T (p.Pro268=) rs1015902038
NM_015512.5(DNAH1):c.8337G>A (p.Val2779=) rs1578186041
NM_015512.5(DNAH1):c.9216G>A (p.Arg3072=) rs1578193087
NM_015512.5(DNAH1):c.9496-5C>T rs1578195290
NM_015512.5(DNAH1):c.9513G>A (p.Val3171=) rs1578195368

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