ClinVar Miner

List of variants in gene DNAH8 reported as likely benign by Invitae

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Gene type:
ClinVar version:
Total variants: 81
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HGVS dbSNP
NM_001206927.2(DNAH8):c.10287A>G (p.Pro3429=) rs369728224
NM_001206927.2(DNAH8):c.10500C>A (p.Ile3500=) rs202065447
NM_001206927.2(DNAH8):c.10637T>C (p.Phe3546Ser) rs142907521
NM_001206927.2(DNAH8):c.10662+8T>C rs1177385307
NM_001206927.2(DNAH8):c.10678G>A (p.Ala3560Thr) rs141263020
NM_001206927.2(DNAH8):c.10707C>T (p.Ala3569=) rs201956190
NM_001206927.2(DNAH8):c.10773C>G (p.Phe3591Leu) rs147574550
NM_001206927.2(DNAH8):c.10794T>G (p.Leu3598=) rs116250863
NM_001206927.2(DNAH8):c.11184C>G (p.Pro3728=) rs114401631
NM_001206927.2(DNAH8):c.11358C>T (p.Thr3786=) rs751697426
NM_001206927.2(DNAH8):c.11379G>A (p.Thr3793=) rs112903128
NM_001206927.2(DNAH8):c.11403A>G (p.Thr3801=) rs1201651090
NM_001206927.2(DNAH8):c.11655A>C (p.Ala3885=) rs145561539
NM_001206927.2(DNAH8):c.12759C>T (p.Asp4253=) rs1487747795
NM_001206927.2(DNAH8):c.12933T>C (p.Asp4311=) rs143973202
NM_001206927.2(DNAH8):c.13053+9A>G rs775870826
NM_001206927.2(DNAH8):c.13083G>A (p.Pro4361=) rs143472136
NM_001206927.2(DNAH8):c.13215-4C>T rs373756546
NM_001206927.2(DNAH8):c.13300C>T (p.Arg4434Trp) rs189023122
NM_001206927.2(DNAH8):c.13381C>T (p.Arg4461Cys) rs143714496
NM_001206927.2(DNAH8):c.13599G>A (p.Ser4533=) rs150470972
NM_001206927.2(DNAH8):c.13683G>T (p.Val4561=) rs201274048
NM_001206927.2(DNAH8):c.13722C>G (p.Leu4574=) rs45600141
NM_001206927.2(DNAH8):c.13748G>T (p.Arg4583Leu) rs139227429
NM_001206927.2(DNAH8):c.13823C>T (p.Thr4608Met) rs142438011
NM_001206927.2(DNAH8):c.13896G>C (p.Gly4632=) rs143487714
NM_001206927.2(DNAH8):c.13992G>C (p.Leu4664=) rs371719991
NM_001206927.2(DNAH8):c.14019C>G (p.Pro4673=) rs142478578
NM_001206927.2(DNAH8):c.14075C>T (p.Pro4692Leu) rs147878071
NM_001206927.2(DNAH8):c.1548A>G (p.Ala516=) rs146078369
NM_001206927.2(DNAH8):c.1704T>C (p.Phe568=) rs773683890
NM_001206927.2(DNAH8):c.1824A>G (p.Glu608=) rs768278758
NM_001206927.2(DNAH8):c.2174C>G (p.Ala725Gly) rs61757621
NM_001206927.2(DNAH8):c.2395+9A>G rs756644206
NM_001206927.2(DNAH8):c.2685A>G (p.Gln895=) rs878854273
NM_001206927.2(DNAH8):c.2719C>T (p.Leu907=) rs1060504238
NM_001206927.2(DNAH8):c.2851C>T (p.Leu951=) rs1554211685
NM_001206927.2(DNAH8):c.3183T>C (p.His1061=) rs751347468
NM_001206927.2(DNAH8):c.3359T>C (p.Ile1120Thr) rs61757622
NM_001206927.2(DNAH8):c.3375C>T (p.Asn1125=) rs1281084129
NM_001206927.2(DNAH8):c.3480C>T (p.Asp1160=) rs139961123
NM_001206927.2(DNAH8):c.3849G>A (p.Glu1283=) rs878854274
NM_001206927.2(DNAH8):c.423A>G (p.Arg141=) rs766979092
NM_001206927.2(DNAH8):c.4512C>T (p.Thr1504=) rs200564814
NM_001206927.2(DNAH8):c.4749C>T (p.Ser1583=) rs749021658
NM_001206927.2(DNAH8):c.5209C>T (p.Arg1737Cys) rs146241522
NM_001206927.2(DNAH8):c.5527G>C (p.Asp1843His) rs61758415
NM_001206927.2(DNAH8):c.5547A>C (p.Ile1849=) rs776384266
NM_001206927.2(DNAH8):c.5550A>G (p.Ser1850=) rs1554229084
NM_001206927.2(DNAH8):c.558T>C (p.Asp186=) rs753974910
NM_001206927.2(DNAH8):c.5808G>A (p.Arg1936=) rs867862598
NM_001206927.2(DNAH8):c.6156C>G (p.Ala2052=) rs775922041
NM_001206927.2(DNAH8):c.6369T>C (p.Pro2123=) rs759664111
NM_001206927.2(DNAH8):c.6528A>C (p.Leu2176=) rs45532134
NM_001206927.2(DNAH8):c.6726G>A (p.Leu2242=) rs878854275
NM_001206927.2(DNAH8):c.684G>A (p.Pro228=) rs202079713
NM_001206927.2(DNAH8):c.6987G>T (p.Val2329=) rs751705607
NM_001206927.2(DNAH8):c.6G>A (p.Glu2=) rs774924483
NM_001206927.2(DNAH8):c.725G>A (p.Arg242His) rs142863013
NM_001206927.2(DNAH8):c.7281C>A (p.Ile2427=) rs544209258
NM_001206927.2(DNAH8):c.7335T>C (p.Ala2445=) rs144391737
NM_001206927.2(DNAH8):c.7471A>G (p.Ile2491Val) rs148698911
NM_001206927.2(DNAH8):c.7584C>T (p.Pro2528=) rs748939836
NM_001206927.2(DNAH8):c.763-7C>A rs1554196154
NM_001206927.2(DNAH8):c.7728A>G (p.Gly2576=) rs140943630
NM_001206927.2(DNAH8):c.7863T>C (p.Asp2621=) rs1554126747
NM_001206927.2(DNAH8):c.788C>A (p.Ala263Glu) rs145115573
NM_001206927.2(DNAH8):c.7920G>A (p.Pro2640=) rs751198406
NM_001206927.2(DNAH8):c.8137-9_8137-7del rs1554127096
NM_001206927.2(DNAH8):c.8238G>C (p.Val2746=) rs147418086
NM_001206927.2(DNAH8):c.8454T>G (p.Ala2818=) rs1403815470
NM_001206927.2(DNAH8):c.8583+10G>T rs146573461
NM_001206927.2(DNAH8):c.8747+4C>T rs201261721
NM_001206927.2(DNAH8):c.8769G>A (p.Glu2923=) rs142674094
NM_001206927.2(DNAH8):c.8871T>A (p.Arg2957=) rs200109265
NM_001206927.2(DNAH8):c.8909C>T (p.Ser2970Phe) rs150571615
NM_001206927.2(DNAH8):c.9087G>A (p.Ser3029=) rs201691475
NM_001206927.2(DNAH8):c.9285T>C (p.Thr3095=) rs144188084
NM_001206927.2(DNAH8):c.9574A>G (p.Met3192Val) rs140935840
NM_001206927.2(DNAH8):c.9643A>T (p.Asn3215Tyr) rs145107574
NM_001206927.2(DNAH8):c.9710T>C (p.Val3237Ala) rs141147863

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