ClinVar Miner

List of variants in gene DNAH11 reported as likely benign for not specified

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Gene type:
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Total variants: 92
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HGVS dbSNP
NM_001277115.2(DNAH11):c.-14C>T rs886038455
NM_001277115.2(DNAH11):c.10411G>A (p.Glu3471Lys) rs117729990
NM_001277115.2(DNAH11):c.10449C>T (p.Ala3483=) rs117000348
NM_001277115.2(DNAH11):c.10485G>A (p.Val3495=) rs771238763
NM_001277115.2(DNAH11):c.1053G>A (p.Glu351=) rs201475447
NM_001277115.2(DNAH11):c.10692-16G>T rs886038456
NM_001277115.2(DNAH11):c.10692-7C>T rs368833367
NM_001277115.2(DNAH11):c.10782G>A (p.Pro3594=) rs72657400
NM_001277115.2(DNAH11):c.11061+10G>A rs755667405
NM_001277115.2(DNAH11):c.11203-4C>T rs200188856
NM_001277115.2(DNAH11):c.11373+17C>T rs563884334
NM_001277115.2(DNAH11):c.11418C>T (p.Phe3806=) rs187814474
NM_001277115.2(DNAH11):c.11497-16C>G rs552675105
NM_001277115.2(DNAH11):c.11508C>G (p.Val3836=) rs199627577
NM_001277115.2(DNAH11):c.11691-20dup rs5882827
NM_001277115.2(DNAH11):c.11718G>C (p.Ala3906=) rs755196801
NM_001277115.2(DNAH11):c.11805G>A (p.Pro3935=) rs187489343
NM_001277115.2(DNAH11):c.11840-20C>T rs146222137
NM_001277115.2(DNAH11):c.12175G>A (p.Ala4059Thr) rs142372794
NM_001277115.2(DNAH11):c.12196-12C>G rs111541378
NM_001277115.2(DNAH11):c.12505C>T (p.Leu4169=) rs764262245
NM_001277115.2(DNAH11):c.12508-14C>T rs886038457
NM_001277115.2(DNAH11):c.12708T>C (p.Asn4236=) rs775042712
NM_001277115.2(DNAH11):c.12899G>A (p.Arg4300His) rs377388499
NM_001277115.2(DNAH11):c.13050-11C>A rs545301825
NM_001277115.2(DNAH11):c.13050-15C>T rs149634292
NM_001277115.2(DNAH11):c.13076G>A (p.Arg4359Gln) rs113653972
NM_001277115.2(DNAH11):c.13163-19T>A rs72658832
NM_001277115.2(DNAH11):c.13257A>G (p.Gly4419=) rs200445638
NM_001277115.2(DNAH11):c.13278A>G (p.Ala4426=) rs773266815
NM_001277115.2(DNAH11):c.1974-20G>A rs886038460
NM_001277115.2(DNAH11):c.2166A>G (p.Pro722=) rs191266255
NM_001277115.2(DNAH11):c.2783A>T (p.Asp928Val) rs201386161
NM_001277115.2(DNAH11):c.297G>T (p.Pro99=) rs886038461
NM_001277115.2(DNAH11):c.3045G>T (p.Glu1015Asp) rs72657303
NM_001277115.2(DNAH11):c.3237T>C (p.Leu1079=) rs72657304
NM_001277115.2(DNAH11):c.3425+5C>G rs776140118
NM_001277115.2(DNAH11):c.3426-18T>G rs886038462
NM_001277115.2(DNAH11):c.3649-20T>C rs886038463
NM_001277115.2(DNAH11):c.3765C>T (p.Asp1255=) rs190062687
NM_001277115.2(DNAH11):c.3766-10C>A rs886038464
NM_001277115.2(DNAH11):c.3853-16T>A rs377295132
NM_001277115.2(DNAH11):c.4125C>A (p.Arg1375=) rs570983771
NM_001277115.2(DNAH11):c.4143G>A (p.Thr1381=) rs757101745
NM_001277115.2(DNAH11):c.4202A>G (p.Gln1401Arg) rs199629774
NM_001277115.2(DNAH11):c.4215C>T (p.Leu1405=) rs886038465
NM_001277115.2(DNAH11):c.4254+13G>A rs371484690
NM_001277115.2(DNAH11):c.4254+8T>C rs771512009
NM_001277115.2(DNAH11):c.4255-12del rs758841984
NM_001277115.2(DNAH11):c.4491G>A (p.Glu1497=) rs564202359
NM_001277115.2(DNAH11):c.4501-7A>T rs62447794
NM_001277115.2(DNAH11):c.4576T>C (p.Leu1526=) rs199559539
NM_001277115.2(DNAH11):c.4620G>A (p.Gln1540=) rs192515447
NM_001277115.2(DNAH11):c.4944+6del rs531049764
NM_001277115.2(DNAH11):c.4945-12T>C rs141572016
NM_001277115.2(DNAH11):c.4945-5T>G rs886038468
NM_001277115.2(DNAH11):c.4961C>G (p.Ala1654Gly) rs376708182
NM_001277115.2(DNAH11):c.5132A>G (p.Gln1711Arg) rs189432084
NM_001277115.2(DNAH11):c.5329-19A>C rs748084989
NM_001277115.2(DNAH11):c.5329-9T>C rs773240082
NM_001277115.2(DNAH11):c.5427C>T (p.Ala1809=) rs372177670
NM_001277115.2(DNAH11):c.5671C>T (p.Pro1891Ser) rs201704416
NM_001277115.2(DNAH11):c.5734A>G (p.Met1912Val) rs886038470
NM_001277115.2(DNAH11):c.5850C>T (p.Ile1950=) rs377208329
NM_001277115.2(DNAH11):c.6041+18T>C rs72657336
NM_001277115.2(DNAH11):c.6042-12T>C rs764234591
NM_001277115.2(DNAH11):c.6181-12T>C rs201203384
NM_001277115.2(DNAH11):c.6273+9A>C rs192777767
NM_001277115.2(DNAH11):c.6416G>A (p.Arg2139Lys) rs140048925
NM_001277115.2(DNAH11):c.6437G>A (p.Arg2146His) rs727505321
NM_001277115.2(DNAH11):c.6607T>C (p.Leu2203=) rs202012891
NM_001277115.2(DNAH11):c.6889C>T (p.Leu2297=) rs886038471
NM_001277115.2(DNAH11):c.6970C>G (p.Leu2324Val) rs201323940
NM_001277115.2(DNAH11):c.7135-18C>T rs886038472
NM_001277115.2(DNAH11):c.7266+5G>A rs149364992
NM_001277115.2(DNAH11):c.7334C>T (p.Ser2445Leu) rs180970138
NM_001277115.2(DNAH11):c.7765G>A (p.Val2589Ile) rs145239537
NM_001277115.2(DNAH11):c.8299G>A (p.Ala2767Thr) rs200628085
NM_001277115.2(DNAH11):c.8478C>T (p.His2826=) rs62445328
NM_001277115.2(DNAH11):c.8647G>A (p.Glu2883Lys) rs752605468
NM_001277115.2(DNAH11):c.8770G>A (p.Val2924Met) rs72657369
NM_001277115.2(DNAH11):c.8798-5G>A rs189821372
NM_001277115.2(DNAH11):c.8829T>C (p.Asp2943=) rs886038474
NM_001277115.2(DNAH11):c.8941-12A>T rs886038475
NM_001277115.2(DNAH11):c.9366T>C (p.Ser3122=) rs886038476
NM_001277115.2(DNAH11):c.9468T>C (p.Asp3156=) rs201207627
NM_001277115.2(DNAH11):c.9598-16G>A rs183862333
NM_001277115.2(DNAH11):c.982+8T>A rs72655978
NM_001277115.2(DNAH11):c.990C>T (p.Leu330=) rs376448045
NM_001277115.2(DNAH11):c.9925-7T>C rs146815254
NM_001277115.2(DNAH11):c.9935A>T (p.Asp3312Val) rs72657389
NM_001277115.2(DNAH11):c.9939G>A (p.Val3313=) rs200349268

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