ClinVar Miner

List of variants in gene DNAH11 reported as benign by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

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Gene type:
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Total variants: 74
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HGVS dbSNP
NM_001277115.2(DNAH11):c.10027-10T>C rs116368970
NM_001277115.2(DNAH11):c.100_101delinsTT (p.Glu34Leu) rs398123604
NM_001277115.2(DNAH11):c.101A>T (p.Glu34Val) rs2285944
NM_001277115.2(DNAH11):c.10399G>A (p.Ala3467Thr) rs2214326
NM_001277115.2(DNAH11):c.1065A>G (p.Pro355=) rs4392792
NM_001277115.2(DNAH11):c.10739G>A (p.Arg3580His) rs34879202
NM_001277115.2(DNAH11):c.10782G>A (p.Pro3594=) rs72657400
NM_001277115.2(DNAH11):c.10976C>T (p.Ala3659Val) rs150631721
NM_001277115.2(DNAH11):c.11122G>T (p.Val3708Leu) rs4722064
NM_001277115.2(DNAH11):c.11200A>C (p.Lys3734Gln) rs114257197
NM_001277115.2(DNAH11):c.11202+13G>A rs73279830
NM_001277115.2(DNAH11):c.11202+7C>A rs73279826
NM_001277115.2(DNAH11):c.11233G>A (p.Glu3745Lys) rs182389910
NM_001277115.2(DNAH11):c.11272T>C (p.Ser3758Pro) rs17145720
NM_001277115.2(DNAH11):c.11298T>C (p.His3766=) rs4722067
NM_001277115.2(DNAH11):c.11325G>A (p.Ala3775=) rs12666072
NM_001277115.2(DNAH11):c.11402C>G (p.Pro3801Arg) rs146362213
NM_001277115.2(DNAH11):c.1199C>T (p.Thr400Ile) rs72655982
NM_001277115.2(DNAH11):c.12288G>A (p.Arg4096=) rs72658820
NM_001277115.2(DNAH11):c.12493A>G (p.Met4165Val) rs6461613
NM_001277115.2(DNAH11):c.12508-12T>C rs72658822
NM_001277115.2(DNAH11):c.12509C>T (p.Thr4170Ile) rs12537531
NM_001277115.2(DNAH11):c.12561T>G (p.Asp4187Glu) rs148429731
NM_001277115.2(DNAH11):c.12644T>C (p.Ile4215Thr) rs150663302
NM_001277115.2(DNAH11):c.12943G>A (p.Ala4315Thr) rs72658825
NM_001277115.2(DNAH11):c.13128C>A (p.Leu4376=) rs56333627
NM_001277115.2(DNAH11):c.13263G>C (p.Pro4421=) rs72658834
NM_001277115.2(DNAH11):c.1426-9T>C rs72655983
NM_001277115.2(DNAH11):c.1702G>A (p.Ala568Thr) rs72655988
NM_001277115.2(DNAH11):c.1916A>G (p.Gln639Arg) rs12670130
NM_001277115.2(DNAH11):c.1956C>T (p.Phe652=) rs6963535
NM_001277115.2(DNAH11):c.1961C>G (p.Ser654Cys) rs62441683
NM_001277115.2(DNAH11):c.2275-15G>T rs60290948
NM_001277115.2(DNAH11):c.2454A>G (p.Ala818=) rs4615458
NM_001277115.2(DNAH11):c.2835A>G (p.Gln945=) rs17144747
NM_001277115.2(DNAH11):c.3068T>C (p.Val1023Ala) rs10269582
NM_001277115.2(DNAH11):c.3112A>G (p.Thr1038Ala) rs10224537
NM_001277115.2(DNAH11):c.3237T>C (p.Leu1079=) rs72657304
NM_001277115.2(DNAH11):c.3256-10C>G rs17745898
NM_001277115.2(DNAH11):c.3384C>T (p.Ser1128=) rs79955190
NM_001277115.2(DNAH11):c.3630G>A (p.Gln1210=) rs3827657
NM_001277115.2(DNAH11):c.3946A>G (p.Met1316Val) rs17144788
NM_001277115.2(DNAH11):c.4377+15A>G rs57208694
NM_001277115.2(DNAH11):c.4430T>C (p.Val1477Ala) rs72657320
NM_001277115.2(DNAH11):c.4449T>C (p.Ile1483=) rs56029521
NM_001277115.2(DNAH11):c.4726-15T>C rs17144822
NM_001277115.2(DNAH11):c.4904A>G (p.Asp1635Gly) rs17144835
NM_001277115.2(DNAH11):c.5152A>G (p.Ile1718Val) rs137855415
NM_001277115.2(DNAH11):c.5490G>A (p.Leu1830=) rs55666134
NM_001277115.2(DNAH11):c.54C>T (p.Thr18=) rs2285942
NM_001277115.2(DNAH11):c.5621+11A>T rs59447021
NM_001277115.2(DNAH11):c.576A>G (p.Ile192Met) rs72655972
NM_001277115.2(DNAH11):c.58C>A (p.Arg20Ser) rs72655967
NM_001277115.2(DNAH11):c.6117G>A (p.Ala2039=) rs78763603
NM_001277115.2(DNAH11):c.6274-13T>G rs2965401
NM_001277115.2(DNAH11):c.6416G>A (p.Arg2139Lys) rs140048925
NM_001277115.2(DNAH11):c.6683+13C>G rs17145077
NM_001277115.2(DNAH11):c.705C>T (p.Asn235=) rs10950854
NM_001277115.2(DNAH11):c.7290C>T (p.Phe2430=) rs12536928
NM_001277115.2(DNAH11):c.7335G>A (p.Ser2445=) rs11768670
NM_001277115.2(DNAH11):c.7552G>A (p.Val2518Ile) rs68023059
NM_001277115.2(DNAH11):c.7570T>C (p.Leu2524=) rs2072220
NM_001277115.2(DNAH11):c.7626G>A (p.Thr2542=) rs2072221
NM_001277115.2(DNAH11):c.7756T>C (p.Tyr2586His) rs2003417
NM_001277115.2(DNAH11):c.7776C>T (p.His2592=) rs1109806
NM_001277115.2(DNAH11):c.7901A>G (p.Asn2634Ser) rs9639393
NM_001277115.2(DNAH11):c.858A>G (p.Glu286=) rs185273259
NM_001277115.2(DNAH11):c.8990G>A (p.Arg2997Gln) rs35865357
NM_001277115.2(DNAH11):c.9097A>G (p.Ile3033Val) rs72657373
NM_001277115.2(DNAH11):c.9102+8G>A rs72657374
NM_001277115.2(DNAH11):c.9337-9T>C rs72657378
NM_001277115.2(DNAH11):c.939C>T (p.Ser313=) rs72655977
NM_001277115.2(DNAH11):c.9435G>A (p.Thr3145=) rs72657379
NM_001277115.2(DNAH11):c.9561G>A (p.Leu3187=) rs6965750

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