ClinVar Miner

List of variants in gene DNAH1 reported as benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 83
Download table as spreadsheet
HGVS dbSNP
NM_015512.4(DNAH1):c.6526-10_6526-9delAT rs562893788
NM_015512.5(DNAH1):c.10305G>A (p.Thr3435=) rs75513160
NM_015512.5(DNAH1):c.10317C>T (p.Ile3439=) rs419050
NM_015512.5(DNAH1):c.10422T>C (p.Leu3474=) rs148913561
NM_015512.5(DNAH1):c.10582C>T (p.Leu3528=) rs202182939
NM_015512.5(DNAH1):c.10881C>A (p.Val3627=) rs11708581
NM_015512.5(DNAH1):c.11043A>G (p.Thr3681=) rs200622578
NM_015512.5(DNAH1):c.11055C>T (p.Ala3685=) rs180952807
NM_015512.5(DNAH1):c.11136G>A (p.Arg3712=) rs147264705
NM_015512.5(DNAH1):c.11230C>T (p.Arg3744Cys) rs419752
NM_015512.5(DNAH1):c.11402G>A (p.Gly3801Asp) rs12163565
NM_015512.5(DNAH1):c.11494C>T (p.Arg3832Cys) rs200962458
NM_015512.5(DNAH1):c.11495= (p.Arg3832=) rs365048
NM_015512.5(DNAH1):c.11495G>A (p.Arg3832His) rs365048
NM_015512.5(DNAH1):c.1172A>G (p.Tyr391Cys) rs181418923
NM_015512.5(DNAH1):c.12375A>T (p.Thr4125=) rs61734637
NM_015512.5(DNAH1):c.1244A>G (p.Lys415Arg) rs61729402
NM_015512.5(DNAH1):c.12626A>G (p.Gln4209Arg) rs202094249
NM_015512.5(DNAH1):c.1321G>C (p.Val441Leu) rs13060192
NM_015512.5(DNAH1):c.1554C>T (p.Ala518=) rs201113513
NM_015512.5(DNAH1):c.1572C>T (p.Thr524=) rs565874512
NM_015512.5(DNAH1):c.1590C>T (p.His530=) rs142935638
NM_015512.5(DNAH1):c.1759A>C (p.Asn587His) rs188699424
NM_015512.5(DNAH1):c.1789C>T (p.Arg597Cys) rs61734654
NM_015512.5(DNAH1):c.1969C>G (p.Pro657Ala) rs199996069
NM_015512.5(DNAH1):c.1981A>G (p.Met661Val) rs61734653
NM_015512.5(DNAH1):c.1986C>T (p.Asp662=) rs376991251
NM_015512.5(DNAH1):c.2204G>A (p.Ser735Asn) rs187636110
NM_015512.5(DNAH1):c.2308C>G (p.Gln770Glu) rs74363541
NM_015512.5(DNAH1):c.2430C>T (p.Thr810=) rs35982798
NM_015512.5(DNAH1):c.2717A>G (p.Asp906Gly) rs61734644
NM_015512.5(DNAH1):c.2724T>C (p.Asn908=) rs201003363
NM_015512.5(DNAH1):c.2744A>G (p.Asn915Ser) rs61734643
NM_015512.5(DNAH1):c.2919C>T (p.His973=) rs149114984
NM_015512.5(DNAH1):c.3090G>A (p.Ala1030=) rs140275399
NM_015512.5(DNAH1):c.3111G>A (p.Ser1037=) rs77639782
NM_015512.5(DNAH1):c.3201C>T (p.Cys1067=) rs114066123
NM_015512.5(DNAH1):c.3694-4C>G rs550254957
NM_015512.5(DNAH1):c.3964A>C (p.Arg1322=) rs11714402
NM_015512.5(DNAH1):c.4080C>T (p.Ile1360=) rs199624371
NM_015512.5(DNAH1):c.4263C>T (p.Pro1421=) rs61739897
NM_015512.5(DNAH1):c.4353G>A (p.Glu1451=) rs560651490
NM_015512.5(DNAH1):c.4504G>A (p.Val1502Met) rs17052095
NM_015512.5(DNAH1):c.4531G>A (p.Val1511Met) rs61734638
NM_015512.5(DNAH1):c.4588A>G (p.Asn1530Asp) rs74498533
NM_015512.5(DNAH1):c.4987C>T (p.Arg1663Cys) rs17052097
NM_015512.5(DNAH1):c.5094+3A>T rs149183773
NM_015512.5(DNAH1):c.5182A>T (p.Ser1728Cys) rs138320093
NM_015512.5(DNAH1):c.5288C>T (p.Ser1763Leu) rs61739896
NM_015512.5(DNAH1):c.5298G>A (p.Gly1766=) rs149285738
NM_015512.5(DNAH1):c.5334G>A (p.Glu1778=) rs61729400
NM_015512.5(DNAH1):c.5611-9G>C rs3752819
NM_015512.5(DNAH1):c.5669G>T (p.Gly1890Val) rs200859252
NM_015512.5(DNAH1):c.5697C>T (p.Tyr1899=) rs115818632
NM_015512.5(DNAH1):c.569T>C (p.Ile190Thr) rs61729450
NM_015512.5(DNAH1):c.5787G>A (p.Ser1929=) rs61738524
NM_015512.5(DNAH1):c.5853G>A (p.Val1951=) rs80128076
NM_015512.5(DNAH1):c.5988A>C (p.Ser1996=) rs61753436
NM_015512.5(DNAH1):c.6139-15G>A rs746239
NM_015512.5(DNAH1):c.6191A>G (p.Asn2064Ser) rs145673040
NM_015512.5(DNAH1):c.6411C>T (p.Asn2137=) rs372595174
NM_015512.5(DNAH1):c.6435A>G (p.Pro2145=) rs372202417
NM_015512.5(DNAH1):c.6819G>A (p.Leu2273=) rs79760452
NM_015512.5(DNAH1):c.6957C>T (p.His2319=) rs1546737
NM_015512.5(DNAH1):c.7020C>T (p.Val2340=) rs200691263
NM_015512.5(DNAH1):c.7143C>G (p.Ile2381Met) rs144580984
NM_015512.5(DNAH1):c.7151A>G (p.Asn2384Ser) rs56002041
NM_015512.5(DNAH1):c.7197G>C (p.Val2399=) rs61738522
NM_015512.5(DNAH1):c.7375G>A (p.Glu2459Lys) rs201064587
NM_015512.5(DNAH1):c.7569C>T (p.Ser2523=) rs73072968
NM_015512.5(DNAH1):c.7572T>C (p.Asp2524=) rs368852045
NM_015512.5(DNAH1):c.7848C>T (p.Tyr2616=) rs113529103
NM_015512.5(DNAH1):c.8134A>G (p.Met2712Val) rs28434358
NM_015512.5(DNAH1):c.8215A>G (p.Ile2739Val) rs61734631
NM_015512.5(DNAH1):c.8266G>A (p.Val2756Met) rs61749019
NM_015512.5(DNAH1):c.8765C>T (p.Ala2922Val) rs182141515
NM_015512.5(DNAH1):c.9121C>T (p.Arg3041Cys) rs61731638
NM_015512.5(DNAH1):c.931G>A (p.Asp311Asn) rs55931436
NM_015512.5(DNAH1):c.933C>T (p.Asp311=) rs199505182
NM_015512.5(DNAH1):c.9624C>T (p.Ile3208=) rs61734628
NM_015512.5(DNAH1):c.9783C>T (p.Arg3261=) rs61733865
NM_015512.5(DNAH1):c.9807C>T (p.Asn3269=) rs199553284
NM_015512.5(DNAH1):c.9935C>T (p.Thr3312Met) rs114919804

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.