ClinVar Miner

List of variants in gene DNAH5 reported as uncertain significance by GeneDx

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Total variants: 17
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HGVS dbSNP
NM_001369.2(DNAH5):c.10415A>G (p.Lys3472Arg) rs1057517890
NM_001369.2(DNAH5):c.11018C>T (p.Ser3673Phe) rs1554034235
NM_001369.2(DNAH5):c.1121T>C (p.Ile374Thr) rs147499872
NM_001369.2(DNAH5):c.11583C>A (p.Ser3861Arg) rs576096758
NM_001369.2(DNAH5):c.13778C>T (p.Thr4593Met) rs142036266
NM_001369.2(DNAH5):c.2052+6_2052+7delinsAG rs1057518277
NM_001369.2(DNAH5):c.2431+5G>A rs369244905
NM_001369.2(DNAH5):c.3320A>T (p.Tyr1107Phe) rs367913308
NM_001369.2(DNAH5):c.3396G>C (p.Lys1132Asn) rs1554087241
NM_001369.2(DNAH5):c.4961G>A (p.Arg1654Gln) rs150868941
NM_001369.2(DNAH5):c.5281C>G (p.Arg1761Gly) rs148891849
NM_001369.2(DNAH5):c.5663C>T (p.Thr1888Ile) rs777579934
NM_001369.2(DNAH5):c.5807C>T (p.Thr1936Ile) rs779609286
NM_001369.2(DNAH5):c.661G>A (p.Val221Met) rs1085307485
NM_001369.2(DNAH5):c.7998G>T (p.Glu2666Asp) rs148720124
NM_001369.2(DNAH5):c.8731A>G (p.Asn2911Asp) rs142852982
NM_001369.2(DNAH5):c.9229C>T (p.Arg3077Trp) rs1426289211

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