ClinVar Miner

List of variants in gene DNAH11 reported as benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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Gene type:
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Total variants: 69
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HGVS dbSNP gnomAD frequency
NM_001277115.2(DNAH11):c.1956C>T (p.Phe652=) rs6963535 0.99232
NM_001277115.2(DNAH11):c.3630G>A (p.Gln1210=) rs3827657 0.78845
NM_001277115.2(DNAH11):c.11298T>C (p.His3766=) rs4722067 0.72158
NM_001277115.2(DNAH11):c.12493A>G (p.Met4165Val) rs6461613 0.69318
NM_001277115.2(DNAH11):c.7776C>T (p.His2592=) rs1109806 0.63800
NM_001277115.2(DNAH11):c.11122G>T (p.Val3708Leu) rs4722064 0.56845
NM_001277115.2(DNAH11):c.7901A>G (p.Asn2634Ser) rs9639393 0.53316
NM_001277115.2(DNAH11):c.4377+15A>G rs57208694 0.50362
NM_001277115.2(DNAH11):c.705C>T (p.Asn235=) rs10950854 0.45869
NM_001277115.2(DNAH11):c.2454A>G (p.Ala818=) rs4615458 0.44959
NM_001277115.2(DNAH11):c.101A>T (p.Glu34Val) rs2285944 0.44739
NM_001277115.2(DNAH11):c.6274-13T>G rs2965401 0.42727
NM_001277115.2(DNAH11):c.7290C>T (p.Phe2430=) rs12536928 0.42173
NM_001277115.2(DNAH11):c.4449T>C (p.Ile1483=) rs56029521 0.39493
NM_001277115.2(DNAH11):c.10399G>A (p.Ala3467Thr) rs2214326 0.38066
NM_001277115.2(DNAH11):c.5621+11A>T rs59447021 0.23311
NM_001277115.2(DNAH11):c.7335G>A (p.Ser2445=) rs11768670 0.20699
NM_001277115.2(DNAH11):c.1916A>G (p.Gln639Arg) rs12670130 0.14853
NM_001277115.2(DNAH11):c.11202+13G>A rs73279830 0.13824
NM_001277115.2(DNAH11):c.1065A>G (p.Pro355=) rs4392792 0.12564
NM_001277115.2(DNAH11):c.7570T>C (p.Leu2524=) rs2072220 0.11781
NM_001277115.2(DNAH11):c.5490G>A (p.Leu1830=) rs55666134 0.11695
NM_001277115.2(DNAH11):c.1961C>G (p.Ser654Cys) rs62441683 0.11359
NM_001277115.2(DNAH11):c.54C>T (p.Thr18=) rs2285942 0.09968
NM_001277115.2(DNAH11):c.11272T>C (p.Ser3758Pro) rs17145720 0.08574
NM_001277115.2(DNAH11):c.2835A>G (p.Gln945=) rs17144747 0.06943
NM_001277115.2(DNAH11):c.4904A>G (p.Asp1635Gly) rs17144835 0.05345
NM_001277115.2(DNAH11):c.11325G>A (p.Ala3775=) rs12666072 0.05248
NM_001277115.2(DNAH11):c.1702G>A (p.Ala568Thr) rs72655988 0.04164
NM_001277115.2(DNAH11):c.1199C>T (p.Thr400Ile) rs72655982 0.04096
NM_001277115.2(DNAH11):c.7756T>C (p.Tyr2586His) rs2003417 0.03454
NM_001277115.2(DNAH11):c.12508-12T>C rs72658822 0.03145
NM_001277115.2(DNAH11):c.12288G>A (p.Arg4096=) rs72658820 0.02841
NM_001277115.2(DNAH11):c.7552G>A (p.Val2518Ile) rs68023059 0.02543
NM_001277115.2(DNAH11):c.12943G>A (p.Ala4315Thr) rs72658825 0.02314
NM_001277115.2(DNAH11):c.6683+13C>G rs17145077 0.01337
NM_001277115.2(DNAH11):c.9337-9T>C rs72657378 0.01332
NM_001277115.2(DNAH11):c.9102+8G>A rs72657374 0.01255
NM_001277115.2(DNAH11):c.12561T>G (p.Asp4187Glu) rs148429731 0.01140
NM_001277115.2(DNAH11):c.8990G>A (p.Arg2997Gln) rs35865357 0.01132
NM_001277115.2(DNAH11):c.3946A>G (p.Met1316Val) rs17144788 0.01127
NM_001277115.2(DNAH11):c.10739G>A (p.Arg3580His) rs34879202 0.00942
NM_001277115.2(DNAH11):c.576A>G (p.Ile192Met) rs72655972 0.00876
NM_001277115.2(DNAH11):c.6117G>A (p.Ala2039=) rs78763603 0.00856
NM_001277115.2(DNAH11):c.11200A>C (p.Lys3734Gln) rs114257197 0.00719
NM_001277115.2(DNAH11):c.1426-9T>C rs72655983 0.00607
NM_001277115.2(DNAH11):c.858A>G (p.Glu286=) rs185273259 0.00504
NM_001277115.2(DNAH11):c.939C>T (p.Ser313=) rs72655977 0.00497
NM_001277115.2(DNAH11):c.2275-15G>T rs60290948 0.00458
NM_001277115.2(DNAH11):c.9435G>A (p.Thr3145=) rs72657379 0.00449
NM_001277115.2(DNAH11):c.10027-10T>C rs116368970 0.00445
NM_001277115.2(DNAH11):c.4726-15T>C rs17144822 0.00445
NM_001277115.2(DNAH11):c.6416G>A (p.Arg2139Lys) rs140048925 0.00445
NM_001277115.2(DNAH11):c.12644T>C (p.Ile4215Thr) rs150663302 0.00428
NM_001277115.2(DNAH11):c.9097A>G (p.Ile3033Val) rs72657373 0.00428
NM_001277115.2(DNAH11):c.4430T>C (p.Val1477Ala) rs72657320 0.00260
NM_001277115.2(DNAH11):c.11233G>A (p.Glu3745Lys) rs182389910 0.00242
NM_001277115.2(DNAH11):c.10782G>A (p.Pro3594=) rs72657400 0.00200
NM_001277115.2(DNAH11):c.58C>A (p.Arg20Ser) rs72655967 0.00188
NM_001277115.2(DNAH11):c.10976C>T (p.Ala3659Val) rs150631721 0.00166
NM_001277115.2(DNAH11):c.11402C>G (p.Pro3801Arg) rs146362213 0.00077
NM_001277115.2(DNAH11):c.5152A>G (p.Ile1718Val) rs137855415 0.00029
NM_001277115.2(DNAH11):c.100_101delinsTT (p.Glu34Leu) rs398123604
NM_001277115.2(DNAH11):c.11202+7C>A rs73279826
NM_001277115.2(DNAH11):c.12509C>T (p.Thr4170Ile) rs12537531
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.7626G>A (p.Thr2542=) rs2072221
NM_001277115.2(DNAH11):c.9561G>A (p.Leu3187=) rs6965750

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