ClinVar Miner

List of variants in gene DNAH8 reported as benign for not specified

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Gene type:
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Total variants: 17
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HGVS dbSNP
NM_001206927.2(DNAH8):c.10141-4del rs11291395
NM_001206927.2(DNAH8):c.11511G>A (p.Arg3837=) rs61748646
NM_001206927.2(DNAH8):c.12451+13A>G rs10947765
NM_001206927.2(DNAH8):c.13054-17T>C rs3737095
NM_001206927.2(DNAH8):c.13119A>G (p.Leu4373=) rs3737094
NM_001206927.2(DNAH8):c.13215-15C>T rs12210777
NM_001206927.2(DNAH8):c.13462A>G (p.Ile4488Val) rs10484847
NM_001206927.2(DNAH8):c.1549T>C (p.Tyr517His) rs61748600
NM_001206927.2(DNAH8):c.1975G>A (p.Ala659Thr) rs61748601
NM_001206927.2(DNAH8):c.3034+9T>C rs12192604
NM_001206927.2(DNAH8):c.3071G>A (p.Gly1024Glu) rs874808
NM_001206927.2(DNAH8):c.3294C>G (p.Ser1098=) rs1678690
NM_001206927.2(DNAH8):c.4300T>C (p.Leu1434=) rs1678729
NM_001206927.2(DNAH8):c.5769C>T (p.His1923=) rs2061907
NM_001206927.2(DNAH8):c.7569G>A (p.Lys2523=) rs9380795
NM_001206927.2(DNAH8):c.7680C>T (p.Val2560=) rs6458080
NM_001206927.2(DNAH8):c.8154C>T (p.Tyr2718=) rs4714192

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