ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 88
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HGVS dbSNP gnomAD frequency
NM_015512.5(DNAH1):c.7805+13A>G rs770284 0.99996
NM_015512.5(DNAH1):c.8150+28T>C rs28481563 0.28676
NM_015512.5(DNAH1):c.3028-41T>C rs35860312 0.28558
NM_015512.5(DNAH1):c.3694-75C>T rs66462821 0.28345
NM_015512.5(DNAH1):c.6957C>T (p.His2319=) rs1546737 0.23926
NM_015512.5(DNAH1):c.10279-17A>C rs192210126 0.23862
NM_015512.5(DNAH1):c.406+221T>C rs11711934 0.20184
NM_015512.5(DNAH1):c.1034-114G>A rs34762015 0.20020
NM_015512.5(DNAH1):c.1445-91T>C rs11718125 0.19459
NM_015512.5(DNAH1):c.3964A>C (p.Arg1322=) rs11714402 0.18733
NM_015512.5(DNAH1):c.1955+205C>T rs11716017 0.18287
NM_015512.5(DNAH1):c.5518+243G>A rs13075370 0.18182
NM_015512.5(DNAH1):c.2300+23G>A rs34355561 0.18166
NM_015512.5(DNAH1):c.11788-52G>A rs390802 0.16174
NM_015512.5(DNAH1):c.11402G>A (p.Gly3801Asp) rs12163565 0.15635
NM_015512.5(DNAH1):c.9003+32G>A rs11721277 0.14445
NM_015512.5(DNAH1):c.12090-256G>A rs56322342 0.14381
NM_015512.5(DNAH1):c.12089+36G>A rs11711974 0.14379
NM_015512.5(DNAH1):c.3859-157G>A rs57849650 0.11894
NM_015512.5(DNAH1):c.3027+85T>C rs62257591 0.10207
NM_015512.5(DNAH1):c.5095-67G>A rs11706515 0.08265
NM_015512.5(DNAH1):c.6139-15G>A rs746239 0.08259
NM_015512.5(DNAH1):c.7151A>G (p.Asn2384Ser) rs56002041 0.07792
NM_015512.5(DNAH1):c.10881C>A (p.Val3627=) rs11708581 0.07706
NM_015512.5(DNAH1):c.9624C>T (p.Ile3208=) rs61734628 0.06095
NM_015512.5(DNAH1):c.11259+278T>C rs71297397 0.05255
NM_015512.5(DNAH1):c.2527-162A>G rs61734645 0.04977
NM_015512.5(DNAH1):c.4087-185G>C rs116084959 0.04073
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.3858+257T>G rs369054867 0.03518
NM_015512.5(DNAH1):c.10475-92G>A rs75648178 0.03067
NM_015512.5(DNAH1):c.5787G>A (p.Ser1929=) rs61738524 0.02555
NM_015512.5(DNAH1):c.4504G>A (p.Val1502Met) rs17052095 0.02539
NM_015512.5(DNAH1):c.3693+155T>C rs114959698 0.02508
NC_000003.12:g.52400530C>A rs28758860 0.02486
NM_015512.5(DNAH1):c.10474+110C>T rs78515185 0.02472
NM_015512.5(DNAH1):c.2526+247A>G rs115136114 0.02445
NM_015512.5(DNAH1):c.12090-266G>A rs115960978 0.02437
NM_015512.5(DNAH1):c.7378-235C>T rs115801815 0.02130
NM_015512.5(DNAH1):c.5288C>T (p.Ser1763Leu) rs61739896 0.01985
NM_015512.5(DNAH1):c.8514+13G>A rs111312769 0.01970
NM_015512.5(DNAH1):c.9783C>T (p.Arg3261=) rs61733865 0.01969
NM_015512.5(DNAH1):c.7848C>T (p.Tyr2616=) rs113529103 0.01967
NM_015512.5(DNAH1):c.9121C>T (p.Arg3041Cys) rs61731638 0.01963
NM_015512.5(DNAH1):c.10627-60G>A rs74357841 0.01962
NM_015512.5(DNAH1):c.11787+161C>T rs79759639 0.01941
NM_015512.5(DNAH1):c.11259+260_11259+262del rs201490355 0.01853
NM_015512.5(DNAH1):c.4531G>A (p.Val1511Met) rs61734638 0.01825
NM_015512.5(DNAH1):c.10305G>A (p.Thr3435=) rs75513160 0.01677
NM_015512.5(DNAH1):c.5697C>T (p.Tyr1899=) rs115818632 0.01673
NM_015512.5(DNAH1):c.739-182C>T rs73837049 0.01660
NM_015512.5(DNAH1):c.2308C>G (p.Gln770Glu) rs74363541 0.01655
NM_015512.5(DNAH1):c.6138+23C>T rs74714472 0.01647
NM_015512.5(DNAH1):c.7569C>T (p.Ser2523=) rs73072968 0.01641
NM_015512.5(DNAH1):c.1789C>T (p.Arg597Cys) rs61734654 0.01589
NM_015512.5(DNAH1):c.931G>A (p.Asp311Asn) rs55931436 0.01502
NM_015512.5(DNAH1):c.7197G>C (p.Val2399=) rs61738522 0.01427
NM_015512.5(DNAH1):c.5988A>C (p.Ser1996=) rs61753436 0.01351
NM_015512.5(DNAH1):c.6191A>G (p.Asn2064Ser) rs145673040 0.00959
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.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.10422T>C (p.Leu3474=) rs148913561 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.7375G>A (p.Glu2459Lys) rs201064587 0.00273
NM_015512.5(DNAH1):c.6819G>A (p.Leu2273=) rs79760452 0.00260
NM_015512.5(DNAH1):c.334-12G>A rs144102868 0.00222
NM_015512.5(DNAH1):c.1590C>T (p.His530=) rs142935638 0.00078
NM_015512.5(DNAH1):c.12626A>G (p.Gln4209Arg) rs202094249 0.00026
NM_015512.5(DNAH1):c.1033+324_1033+333del rs36097098
NM_015512.5(DNAH1):c.11494C>T (p.Arg3832Cys) rs200962458
NM_015512.5(DNAH1):c.2107-82C>T rs7633687
NM_015512.5(DNAH1):c.3481-193dup rs551410758
NM_015512.5(DNAH1):c.407-184C>T rs11710014
NM_015512.5(DNAH1):c.4266+124G>A rs11707864
NM_015512.5(DNAH1):c.4407+40C>G rs2306864
NM_015512.5(DNAH1):c.5244+259G>A rs56899118
NM_015512.5(DNAH1):c.5611-9G>C rs3752819
NM_015512.5(DNAH1):c.5765+206A>G rs79779473
NM_015512.5(DNAH1):c.6985+90T>C rs116620381
NM_015512.5(DNAH1):c.6986-185del rs36095568
NM_015512.5(DNAH1):c.8626-302_8626-299del rs113576425
NM_015512.5(DNAH1):c.8811+53G>A rs11720365

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