ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 85
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HGVS dbSNP gnomAD frequency
NM_001277115.2(DNAH11):c.6416G>A (p.Arg2139Lys) rs140048925 0.00483
NM_001277115.2(DNAH11):c.4501-7A>T rs62447794 0.00461
NM_001277115.2(DNAH11):c.6041+18T>C rs72657336 0.00425
NM_001277115.2(DNAH11):c.8478C>T (p.His2826=) rs62445328 0.00419
NM_001277115.2(DNAH11):c.11805G>A (p.Pro3935=) rs187489343 0.00361
NM_001277115.2(DNAH11):c.9935A>T (p.Asp3312Val) rs72657389 0.00307
NM_001277115.2(DNAH11):c.13163-19T>A rs72658832 0.00299
NM_001277115.2(DNAH11):c.9468T>C (p.Asp3156=) rs201207627 0.00299
NM_001277115.2(DNAH11):c.8798-5G>A rs189821372 0.00292
NM_001277115.2(DNAH11):c.9598-16G>A rs183862333 0.00226
NM_001277115.2(DNAH11):c.7765G>A (p.Val2589Ile) rs145239537 0.00220
NM_001277115.2(DNAH11):c.10782G>A (p.Pro3594=) rs72657400 0.00213
NM_001277115.2(DNAH11):c.13076G>A (p.Arg4359Gln) rs113653972 0.00212
NM_001277115.2(DNAH11):c.12196-12C>G rs111541378 0.00206
NM_001277115.2(DNAH11):c.11840-20C>T rs146222137 0.00183
NM_001277115.2(DNAH11):c.12175G>A (p.Ala4059Thr) rs142372794 0.00168
NM_001277115.2(DNAH11):c.6970C>G (p.Leu2324Val) rs201323940 0.00150
NM_001277115.2(DNAH11):c.6181-12T>C rs201203384 0.00122
NM_001277115.2(DNAH11):c.13257A>G (p.Gly4419=) rs200445638 0.00103
NM_001277115.2(DNAH11):c.3765C>T (p.Asp1255=) rs190062687 0.00092
NM_001277115.2(DNAH11):c.11203-4C>T rs200188856 0.00088
NM_001277115.2(DNAH11):c.4202A>G (p.Gln1401Arg) rs199629774 0.00074
NM_001277115.2(DNAH11):c.2166A>G (p.Pro722=) rs191266255 0.00069
NM_001277115.2(DNAH11):c.7266+5G>A rs149364992 0.00069
NM_001277115.2(DNAH11):c.9939G>A (p.Val3313=) rs200349268 0.00069
NM_001277115.2(DNAH11):c.4576T>C (p.Leu1526=) rs199559539 0.00047
NM_001277115.2(DNAH11):c.4961C>G (p.Ala1654Gly) rs376708182 0.00044
NM_001277115.2(DNAH11):c.5671C>T (p.Pro1891Ser) rs201704416 0.00039
NM_001277115.2(DNAH11):c.11418C>T (p.Phe3806=) rs187814474 0.00036
NM_001277115.2(DNAH11):c.10692-7C>T rs368833367 0.00031
NM_001277115.2(DNAH11):c.5132A>G (p.Gln1711Arg) rs189432084 0.00031
NM_001277115.2(DNAH11):c.10411G>A (p.Glu3471Lys) rs117729990 0.00024
NM_001277115.2(DNAH11):c.4945-12T>C rs141572016 0.00024
NM_001277115.2(DNAH11):c.12899G>A (p.Arg4300His) rs377388499 0.00023
NM_001277115.2(DNAH11):c.4254+13G>A rs371484690 0.00021
NM_001277115.2(DNAH11):c.9925-7T>C rs146815254 0.00021
NM_001277115.2(DNAH11):c.982+8T>A rs72655978 0.00019
NM_001277115.2(DNAH11):c.8770G>A (p.Val2924Met) rs72657369 0.00018
NM_001277115.2(DNAH11):c.4620G>A (p.Gln1540=) rs192515447 0.00013
NM_001277115.2(DNAH11):c.8299G>A (p.Ala2767Thr) rs200628085 0.00010
NM_001277115.2(DNAH11):c.10449C>T (p.Ala3483=) rs117000348 0.00009
NM_001277115.2(DNAH11):c.11497-16C>G rs552675105 0.00006
NM_001277115.2(DNAH11):c.6607T>C (p.Leu2203=) rs202012891 0.00005
NM_001277115.2(DNAH11):c.4944+6del rs531049764 0.00004
NM_001277115.2(DNAH11):c.5850C>T (p.Ile1950=) rs377208329 0.00004
NM_001277115.2(DNAH11):c.10485G>A (p.Val3495=) rs771238763 0.00003
NM_001277115.2(DNAH11):c.4254+8T>C rs771512009 0.00003
NM_001277115.2(DNAH11):c.8647G>A (p.Glu2883Lys) rs752605468 0.00003
NM_001277115.2(DNAH11):c.1053G>A (p.Glu351=) rs201475447 0.00002
NM_001277115.2(DNAH11):c.4143G>A (p.Thr1381=) rs757101745 0.00002
NM_001277115.2(DNAH11):c.7334C>T (p.Ser2445Leu) rs180970138 0.00002
NM_001277115.2(DNAH11):c.8941-12A>T rs886038475 0.00002
NM_001277115.2(DNAH11):c.11061+10G>A rs755667405 0.00001
NM_001277115.2(DNAH11):c.12508-14C>T rs886038457 0.00001
NM_001277115.2(DNAH11):c.3649-20T>C rs886038463 0.00001
NM_001277115.2(DNAH11):c.4215C>T (p.Leu1405=) rs886038465 0.00001
NM_001277115.2(DNAH11):c.4491G>A (p.Glu1497=) rs564202359 0.00001
NM_001277115.2(DNAH11):c.5329-9T>C rs773240082 0.00001
NM_001277115.2(DNAH11):c.5734A>G (p.Met1912Val) rs886038470 0.00001
NM_001277115.2(DNAH11):c.6042-12T>C rs764234591 0.00001
NM_001277115.2(DNAH11):c.7135-18C>T rs886038472 0.00001
NM_001277115.2(DNAH11):c.990C>T (p.Leu330=) rs376448045 0.00001
NM_001277115.2(DNAH11):c.-14C>T rs886038455
NM_001277115.2(DNAH11):c.10692-16G>T rs886038456
NM_001277115.2(DNAH11):c.11373+17C>T rs563884334
NM_001277115.2(DNAH11):c.11508C>G (p.Val3836=) rs199627577
NM_001277115.2(DNAH11):c.11718G>C (p.Ala3906=) rs755196801
NM_001277115.2(DNAH11):c.12505C>T (p.Leu4169=) rs764262245
NM_001277115.2(DNAH11):c.12708T>C (p.Asn4236=) rs775042712
NM_001277115.2(DNAH11):c.13278A>G (p.Ala4426=) rs773266815
NM_001277115.2(DNAH11):c.1974-20G>A rs886038460
NM_001277115.2(DNAH11):c.297G>T (p.Pro99=) rs886038461
NM_001277115.2(DNAH11):c.3426-18T>G rs886038462
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.4255-12del rs758841984
NM_001277115.2(DNAH11):c.4945-5T>G rs886038468
NM_001277115.2(DNAH11):c.5329-19A>C rs748084989
NM_001277115.2(DNAH11):c.5427C>T (p.Ala1809=) rs372177670
NM_001277115.2(DNAH11):c.6273+9A>C rs192777767
NM_001277115.2(DNAH11):c.6437G>A (p.Arg2146His) rs727505321
NM_001277115.2(DNAH11):c.6889C>T (p.Leu2297=) rs886038471
NM_001277115.2(DNAH11):c.8829T>C (p.Asp2943=) rs886038474
NM_001277115.2(DNAH11):c.9366T>C (p.Ser3122=) rs886038476

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