ClinVar Miner

List of variants in gene DYNC2H1 reported as uncertain significance for not specified

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Total variants: 15
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HGVS dbSNP
NM_001080463.1(DYNC2H1):c.11413A>G (p.Thr3805Ala) rs764785064
NM_001080463.1(DYNC2H1):c.11510A>G (p.Tyr3837Cys) rs757922501
NM_001080463.1(DYNC2H1):c.11530A>G (p.Lys3844Glu) rs1434517868
NM_001080463.1(DYNC2H1):c.1263C>A (p.Phe421Leu) rs142881106
NM_001080463.1(DYNC2H1):c.12833T>G (p.Val4278Gly) rs913559604
NM_001080463.1(DYNC2H1):c.1720C>A (p.His574Asn) rs1045577540
NM_001080463.1(DYNC2H1):c.3365A>C (p.Lys1122Thr) rs749093220
NM_001080463.1(DYNC2H1):c.3419G>T (p.Gly1140Val) rs201043335
NM_001080463.1(DYNC2H1):c.3682C>A (p.Leu1228Ile) rs189806840
NM_001080463.1(DYNC2H1):c.5180T>C (p.Ile1727Thr) rs1478814855
NM_001080463.1(DYNC2H1):c.5642G>A (p.Arg1881Lys) rs199541807
NM_001080463.1(DYNC2H1):c.5695G>A (p.Val1899Ile) rs150887098
NM_001080463.1(DYNC2H1):c.6115C>T (p.Arg2039Cys) rs779111999
NM_001080463.1(DYNC2H1):c.8365T>C (p.Phe2789Leu) rs184910011
NM_001080463.1(DYNC2H1):c.954A>G (p.Lys318=) rs778594253

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