ClinVar Miner

List of variants in gene DNAH11 reported as benign by Illumina Laboratory Services, Illumina

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Gene type:
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Total variants: 18
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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 0.69063
NM_001277115.2(DNAH11):c.7776C>T (p.His2592=) rs1109806 0.63800
NM_001277115.2(DNAH11):c.11122G>T (p.Val3708Leu) rs4722064 0.57409
NM_001277115.2(DNAH11):c.7901A>G (p.Asn2634Ser) rs9639393 0.53316
NM_001277115.2(DNAH11):c.4377+15A>G rs57208694 0.50202
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 0.44667
NM_001277115.2(DNAH11):c.100G>T (p.Glu34Ter) rs2285943 0.44658
NM_001277115.2(DNAH11):c.6274-13T>G rs2965401 0.42569
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.6547-5C>G rs115200161 0.01380
NM_001277115.2(DNAH11):c.7626G>A (p.Thr2542=) rs2072221

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