ClinVar Miner

List of variants in gene DNAH5 reported as uncertain significance by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

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Total variants: 18
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HGVS dbSNP
NM_001369.2(DNAH5):c.10195G>A (p.Val3399Ile) rs749397968
NM_001369.2(DNAH5):c.11437C>T (p.Arg3813Trp) rs140948493
NM_001369.2(DNAH5):c.11869G>A (p.Asp3957Asn) rs749548708
NM_001369.2(DNAH5):c.11974G>C (p.Asp3992His) rs143251480
NM_001369.2(DNAH5):c.1206T>A (p.Asn402Lys) rs140782270
NM_001369.2(DNAH5):c.12209C>T (p.Thr4070Ile) rs746662023
NM_001369.2(DNAH5):c.1715T>G (p.Leu572Trp) rs137878131
NM_001369.2(DNAH5):c.3895G>T (p.Val1299Phe) rs767853104
NM_001369.2(DNAH5):c.5485-11A>G rs372860402
NM_001369.2(DNAH5):c.6305G>A (p.Arg2102His) rs876657782
NM_001369.2(DNAH5):c.6579+3A>G rs727502976
NM_001369.2(DNAH5):c.6731A>T (p.Lys2244Met) rs187023993
NM_001369.2(DNAH5):c.7502G>C (p.Arg2501Pro) rs78853309
NM_001369.2(DNAH5):c.7531C>T (p.Arg2511Trp) rs564040169
NM_001369.2(DNAH5):c.7998G>T (p.Glu2666Asp) rs148720124
NM_001369.2(DNAH5):c.8128G>A
NM_001369.2(DNAH5):c.8387A>G (p.Asp2796Gly) rs727502974
NM_001369.2(DNAH5):c.8840C>T (p.Thr2947Ile) rs756216163

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