ClinVar Miner

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

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Total variants: 18
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HGVS dbSNP
NM_001277115.2(DNAH11):c.10411G>A (p.Glu3471Lys) rs117729990
NM_001277115.2(DNAH11):c.11418C>T (p.Phe3806=) rs187814474
NM_001277115.2(DNAH11):c.12175G>A (p.Ala4059Thr) rs142372794
NM_001277115.2(DNAH11):c.12708T>C (p.Asn4236=) rs775042712
NM_001277115.2(DNAH11):c.12899G>A (p.Arg4300His) rs377388499
NM_001277115.2(DNAH11):c.13050-15C>T rs149634292
NM_001277115.2(DNAH11):c.2166A>G (p.Pro722=) rs191266255
NM_001277115.2(DNAH11):c.4254+13G>A rs371484690
NM_001277115.2(DNAH11):c.4501-7A>T rs62447794
NM_001277115.2(DNAH11):c.4945-12T>C rs141572016
NM_001277115.2(DNAH11):c.5132A>G (p.Gln1711Arg) rs189432084
NM_001277115.2(DNAH11):c.6437G>A (p.Arg2146His) rs727505321
NM_001277115.2(DNAH11):c.6970C>G (p.Leu2324Val) rs201323940
NM_001277115.2(DNAH11):c.8647G>A (p.Glu2883Lys) rs752605468
NM_001277115.2(DNAH11):c.8770G>A (p.Val2924Met) rs72657369
NM_001277115.2(DNAH11):c.8798-5G>A rs189821372
NM_001277115.2(DNAH11):c.990C>T (p.Leu330=) rs376448045
NM_001277115.2(DNAH11):c.9935A>T (p.Asp3312Val) rs72657389

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