ClinVar Miner

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

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Gene type:
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Total variants: 19
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HGVS dbSNP
NM_001277115.2(DNAH11):c.100G>T (p.Glu34Ter) rs2285943
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.11122G>T (p.Val3708Leu) rs4722064
NM_001277115.2(DNAH11):c.11298T>C (p.His3766=) rs4722067
NM_001277115.2(DNAH11):c.12493A>G (p.Met4165Val) rs6461613
NM_001277115.2(DNAH11):c.1956C>T (p.Phe652=) rs6963535
NM_001277115.2(DNAH11):c.2454A>G (p.Ala818=) rs4615458
NM_001277115.2(DNAH11):c.3112A>G (p.Thr1038Ala) rs10224537
NM_001277115.2(DNAH11):c.3630G>A (p.Gln1210=) rs3827657
NM_001277115.2(DNAH11):c.4377+15A>G rs57208694
NM_001277115.2(DNAH11):c.4449T>C (p.Ile1483=) rs56029521
NM_001277115.2(DNAH11):c.6274-13T>G rs2965401
NM_001277115.2(DNAH11):c.6547-5C>G rs115200161
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.7626G>A (p.Thr2542=) rs2072221
NM_001277115.2(DNAH11):c.7776C>T (p.His2592=) rs1109806
NM_001277115.2(DNAH11):c.7901A>G (p.Asn2634Ser) rs9639393

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