ClinVar Miner

List of variants in gene DNAH8 reported as benign by Invitae

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Gene type:
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Total variants: 69
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HGVS dbSNP
NM_001206927.2(DNAH8):c.10173G>A (p.Arg3391=) rs370433159
NM_001206927.2(DNAH8):c.10179T>G (p.Leu3393=) rs146031264
NM_001206927.2(DNAH8):c.1050C>T (p.Ala350=) rs9470924
NM_001206927.2(DNAH8):c.10591C>T (p.Leu3531=) rs150730516
NM_001206927.2(DNAH8):c.1095A>G (p.Val365=) rs142065001
NM_001206927.2(DNAH8):c.1110C>T (p.Ile370=) rs200423630
NM_001206927.2(DNAH8):c.11204A>G (p.His3735Arg) rs77540135
NM_001206927.2(DNAH8):c.11331T>A (p.Thr3777=) rs75954496
NM_001206927.2(DNAH8):c.11340A>G (p.Leu3780=) rs113024778
NM_001206927.2(DNAH8):c.11361A>G (p.Pro3787=) rs111791517
NM_001206927.2(DNAH8):c.11511G>A (p.Arg3837=) rs61748646
NM_001206927.2(DNAH8):c.11580C>T (p.Asp3860=) rs149356438
NM_001206927.2(DNAH8):c.11771C>T (p.Thr3924Met) rs61757218
NM_001206927.2(DNAH8):c.11776T>C (p.Leu3926=) rs148084212
NM_001206927.2(DNAH8):c.11817-7G>A rs139673856
NM_001206927.2(DNAH8):c.11853A>G (p.Thr3951=) rs115871283
NM_001206927.2(DNAH8):c.11895T>C (p.Ser3965=) rs151015092
NM_001206927.2(DNAH8):c.11997T>C (p.Ala3999=) rs148812133
NM_001206927.2(DNAH8):c.12137G>A (p.Arg4046His) rs139446902
NM_001206927.2(DNAH8):c.12264C>T (p.Asp4088=) rs61748647
NM_001206927.2(DNAH8):c.12526-3C>T rs374461538
NM_001206927.2(DNAH8):c.12567A>C (p.Glu4189Asp) rs61757618
NM_001206927.2(DNAH8):c.12591G>A (p.Thr4197=) rs59067570
NM_001206927.2(DNAH8):c.12969G>A (p.Thr4323=) rs114095356
NM_001206927.2(DNAH8):c.13214+10T>C rs112998568
NM_001206927.2(DNAH8):c.13468C>T (p.Arg4490Cys) rs78849281
NM_001206927.2(DNAH8):c.14100G>T (p.Val4700=) rs113990988
NM_001206927.2(DNAH8):c.1617+3T>G rs58784538
NM_001206927.2(DNAH8):c.1764+2T>C rs77769111
NM_001206927.2(DNAH8):c.1884A>G (p.Gln628=) rs149534667
NM_001206927.2(DNAH8):c.1920C>T (p.Asp640=) rs78139815
NM_001206927.2(DNAH8):c.2037A>G (p.Gln679=) rs761979645
NM_001206927.2(DNAH8):c.2526G>A (p.Gln842=) rs141289823
NM_001206927.2(DNAH8):c.2549A>G (p.Glu850Gly) rs117061525
NM_001206927.2(DNAH8):c.2620G>A (p.Val874Met) rs45529837
NM_001206927.2(DNAH8):c.270G>C (p.Pro90=) rs180723141
NM_001206927.2(DNAH8):c.2915A>T (p.Glu972Val) rs139961713
NM_001206927.2(DNAH8):c.3035-4A>G rs185584533
NM_001206927.2(DNAH8):c.3294C>A (p.Ser1098=) rs1678690
NM_001206927.2(DNAH8):c.3419A>G (p.His1140Arg) rs377516809
NM_001206927.2(DNAH8):c.4084-4G>T rs61748602
NM_001206927.2(DNAH8):c.4265G>A (p.Arg1422His) rs145309531
NM_001206927.2(DNAH8):c.4383G>A (p.Leu1461=) rs145272110
NM_001206927.2(DNAH8):c.4401G>A (p.Thr1467=) rs45622336
NM_001206927.2(DNAH8):c.4449G>A (p.Glu1483=) rs61757623
NM_001206927.2(DNAH8):c.4881C>T (p.Ile1627=) rs200549336
NM_001206927.2(DNAH8):c.4908G>T (p.Glu1636Asp) rs61757219
NM_001206927.2(DNAH8):c.5127C>T (p.Leu1709=) rs61748643
NM_001206927.2(DNAH8):c.5196T>C (p.Pro1732=) rs1678744
NM_001206927.2(DNAH8):c.5364-5T>G rs200015017
NM_001206927.2(DNAH8):c.5490C>A (p.Asp1830Glu) rs45519938
NM_001206927.2(DNAH8):c.5541C>T (p.Ala1847=) rs1678746
NM_001206927.2(DNAH8):c.5701C>T (p.Leu1901Phe) rs111580219
NM_001206927.2(DNAH8):c.6966A>T (p.Pro2322=) rs149125241
NM_001206927.2(DNAH8):c.7171G>T (p.Ala2391Ser) rs61758417
NM_001206927.2(DNAH8):c.724C>T (p.Arg242Cys) rs79455046
NM_001206927.2(DNAH8):c.7551T>C (p.Asp2517=) rs78611987
NM_001206927.2(DNAH8):c.7982C>A (p.Thr2661Asn) rs862432
NM_001206927.2(DNAH8):c.8088A>G (p.Leu2696=) rs59600851
NM_001206927.2(DNAH8):c.8259+6G>A rs112605623
NM_001206927.2(DNAH8):c.832A>G (p.Ile278Val) rs147580001
NM_001206927.2(DNAH8):c.8338A>G (p.Ile2780Val) rs116401640
NM_001206927.2(DNAH8):c.8339T>C (p.Ile2780Thr) rs142328376
NM_001206927.2(DNAH8):c.8524A>G (p.Ile2842Val) rs377381072
NM_001206927.2(DNAH8):c.863A>G (p.Asn288Ser) rs6935293
NM_001206927.2(DNAH8):c.8724G>A (p.Glu2908=) rs149787191
NM_001206927.2(DNAH8):c.9859+7GGAAT[2] rs878854276
NM_001206927.2(DNAH8):c.9943G>A (p.Ala3315Thr) rs76387239
NM_001206927.2(DNAH8):c.9987C>T (p.Ser3329=) rs150857304

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