ClinVar Miner

List of variants in gene DYNC2H1 reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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Total variants: 28
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HGVS dbSNP
NM_001377.3(DYNC2H1):c.10157T>C (p.Ile3386Thr) rs542490708
NM_001377.3(DYNC2H1):c.11509A>G (p.Lys3837Glu) rs1434517868
NM_001377.3(DYNC2H1):c.1263C>A (p.Phe421Leu) rs142881106
NM_001377.3(DYNC2H1):c.12812T>G (p.Val4271Gly) rs913559604
NM_001377.3(DYNC2H1):c.12909C>A (p.Phe4303Leu) rs191971137
NM_001377.3(DYNC2H1):c.1720C>A (p.His574Asn) rs1045577540
NM_001377.3(DYNC2H1):c.1757T>G (p.Val586Gly) rs864622357
NM_001377.3(DYNC2H1):c.2996C>T (p.Thr999Ile) rs753542063
NM_001377.3(DYNC2H1):c.3419G>T (p.Gly1140Val) rs201043335
NM_001377.3(DYNC2H1):c.3682C>A (p.Leu1228Ile) rs189806840
NM_001377.3(DYNC2H1):c.4073G>A (p.Arg1358His) rs184256941
NM_001377.3(DYNC2H1):c.4916C>A (p.Thr1639Lys) rs200239560
NM_001377.3(DYNC2H1):c.5180T>C (p.Ile1727Thr) rs1478814855
NM_001377.3(DYNC2H1):c.5642G>A (p.Arg1881Lys) rs199541807
NM_001377.3(DYNC2H1):c.5695G>A (p.Val1899Ile) rs150887098
NM_001377.3(DYNC2H1):c.6047A>G (p.Tyr2016Cys) rs200190291
NM_001377.3(DYNC2H1):c.6093T>G (p.Asp2031Glu) rs372641908
NM_001377.3(DYNC2H1):c.6115C>T (p.Arg2039Cys) rs779111999
NM_001377.3(DYNC2H1):c.6551A>T (p.Asp2184Val) rs201967064
NM_001377.3(DYNC2H1):c.7462G>A (p.Asp2488Asn) rs201825699
NM_001377.3(DYNC2H1):c.8102C>T (p.Ala2701Val) rs765998830
NM_001377.3(DYNC2H1):c.8365T>C (p.Phe2789Leu) rs184910011
NM_001377.3(DYNC2H1):c.8882C>T (p.Ala2961Val) rs900234882
NM_001377.3(DYNC2H1):c.9254C>T (p.Ala3085Val) rs202071528
NM_001377.3(DYNC2H1):c.9505A>G (p.Ile3169Val) rs200170585
NM_001377.3(DYNC2H1):c.9585G>C (p.Glu3195Asp) rs758118161
NM_001377.3(DYNC2H1):c.9814T>A (p.Leu3272Ile) rs200342335
NM_001377.3(DYNC2H1):c.9842T>C (p.Ile3281Thr) rs1204094235

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