ClinVar Miner

List of variants in gene DYNC1H1 reported as likely benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_001376.5(DYNC1H1):c.11942C>G (p.Thr3981Arg) rs138428684 0.00288
NM_001376.5(DYNC1H1):c.2719-6C>T rs199763298 0.00078
NM_001376.5(DYNC1H1):c.5310C>T (p.Gly1770=) rs34013442 0.00078
NM_001376.5(DYNC1H1):c.12258C>T (p.Thr4086=) rs141242095 0.00059
NM_001376.5(DYNC1H1):c.12513+17C>T rs368189529 0.00027
NM_001376.5(DYNC1H1):c.13707G>A (p.Thr4569=) rs138571942 0.00023
NM_001376.5(DYNC1H1):c.13808G>T (p.Ser4603Ile) rs200731839 0.00020
NM_001376.5(DYNC1H1):c.8478A>G (p.Ala2826=) rs117846737 0.00016
NM_001376.5(DYNC1H1):c.12333G>A (p.Lys4111=) rs373520665 0.00012
NM_001376.5(DYNC1H1):c.657G>A (p.Gln219=) rs374440380 0.00011
NM_001376.5(DYNC1H1):c.7317C>T (p.His2439=) rs200197781 0.00010
NM_001376.5(DYNC1H1):c.318C>T (p.Asp106=) rs752702437 0.00006
NM_001376.5(DYNC1H1):c.10941G>A (p.Pro3647=) rs374214760 0.00004
NM_001376.5(DYNC1H1):c.10548C>T (p.Tyr3516=) rs760532492 0.00003
NM_001376.5(DYNC1H1):c.6249A>G (p.Gln2083=) rs754533185 0.00001
NM_001376.5(DYNC1H1):c.1461+10G>A rs368817833
NM_001376.5(DYNC1H1):c.3015+18C>G rs2749894
NM_001376.5(DYNC1H1):c.7968A>G (p.Gly2656=) rs2048333565
NM_001376.5(DYNC1H1):c.9726G>A (p.Lys3242=)

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