ClinVar Miner

List of variants in gene DYNC2H1 reported as uncertain significance by GeneDx

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Total variants: 21
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HGVS dbSNP
NM_001377.3(DYNC2H1):c.10664T>C (p.Val3555Ala) rs1555082969
NM_001377.3(DYNC2H1):c.10883C>T (p.Thr3628Ile) rs1057524234
NM_001377.3(DYNC2H1):c.11263A>G (p.Met3755Val) rs137853026
NM_001377.3(DYNC2H1):c.11429C>G (p.Thr3810Ser) rs1555096677
NM_001377.3(DYNC2H1):c.11629A>G (p.Arg3877Gly) rs1194851950
NM_001377.3(DYNC2H1):c.12317T>C (p.Leu4106Ser) rs369591902
NM_001377.3(DYNC2H1):c.12439C>T (p.Arg4147Cys) rs755441612
NM_001377.3(DYNC2H1):c.1263C>A (p.Phe421Leu) rs142881106
NM_001377.3(DYNC2H1):c.1288C>T (p.Arg430Cys) rs374073337
NM_001377.3(DYNC2H1):c.12916A>C (p.Asn4306His) rs200264343
NM_001377.3(DYNC2H1):c.2289G>C (p.Met763Ile) rs1057524436
NM_001377.3(DYNC2H1):c.3794G>A (p.Arg1265His) rs200635842
NM_001377.3(DYNC2H1):c.5060C>T (p.Pro1687Leu) rs376385873
NM_001377.3(DYNC2H1):c.5389G>A (p.Gly1797Ser) rs1064796293
NM_001377.3(DYNC2H1):c.5821G>C (p.Ala1941Pro) rs368058473
NM_001377.3(DYNC2H1):c.6019A>G (p.Thr2007Ala) rs1064796480
NM_001377.3(DYNC2H1):c.6047A>G (p.Tyr2016Cys) rs200190291
NM_001377.3(DYNC2H1):c.6625A>T (p.Thr2209Ser) rs200762072
NM_001377.3(DYNC2H1):c.8782A>C (p.Lys2928Gln) rs190819700
NM_001377.3(DYNC2H1):c.9242G>A (p.Arg3081His) rs749753983
NM_001377.3(DYNC2H1):c.9814T>A (p.Leu3272Ile) rs200342335

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