ClinVar Miner

List of variants in gene DYNC1H1 reported as benign for not provided

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Gene type:
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Total variants: 76
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HGVS dbSNP
NM_001376.5(DYNC1H1):c.10065T>C (p.Ser3355=) rs80096622
NM_001376.5(DYNC1H1):c.10079+93C>G
NM_001376.5(DYNC1H1):c.10413+93G>A
NM_001376.5(DYNC1H1):c.11207-75del
NM_001376.5(DYNC1H1):c.11532G>A (p.Pro3844=) rs372511563
NM_001376.5(DYNC1H1):c.11596-7G>A rs375593873
NM_001376.5(DYNC1H1):c.11685C>T (p.Thr3895=) rs17541519
NM_001376.5(DYNC1H1):c.11690+239A>G
NM_001376.5(DYNC1H1):c.11941+55G>C
NM_001376.5(DYNC1H1):c.11942C>G (p.Thr3981Arg) rs138428684
NM_001376.5(DYNC1H1):c.12087C>A (p.His4029Gln) rs10129889
NM_001376.5(DYNC1H1):c.12453A>T (p.Pro4151=)
NM_001376.5(DYNC1H1):c.12513+10T>G rs17512839
NM_001376.5(DYNC1H1):c.12514-259G>C
NM_001376.5(DYNC1H1):c.12684+46A>G
NM_001376.5(DYNC1H1):c.12902+35G>A
NM_001376.5(DYNC1H1):c.12902+46G>A
NM_001376.5(DYNC1H1):c.13006+276C>G
NM_001376.5(DYNC1H1):c.13218+70T>G
NM_001376.5(DYNC1H1):c.13219-140G>A
NM_001376.5(DYNC1H1):c.13372+165A>G
NM_001376.5(DYNC1H1):c.13372+9G>A rs1004903
NM_001376.5(DYNC1H1):c.13373-273G>C
NM_001376.5(DYNC1H1):c.13685-81_13685-36dup
NM_001376.5(DYNC1H1):c.1462-323G>A
NM_001376.5(DYNC1H1):c.1462-41G>A
NM_001376.5(DYNC1H1):c.1587C>T (p.Asn529=) rs138418906
NM_001376.5(DYNC1H1):c.2025T>C (p.Asn675=) rs140154194
NM_001376.5(DYNC1H1):c.2538+10C>T
NM_001376.5(DYNC1H1):c.2538+230A>G
NM_001376.5(DYNC1H1):c.2538+303A>G
NM_001376.5(DYNC1H1):c.2718+146A>G
NM_001376.5(DYNC1H1):c.2718+243T>C
NM_001376.5(DYNC1H1):c.2719-107C>A
NM_001376.5(DYNC1H1):c.2721T>C (p.Ile907=) rs114021657
NM_001376.5(DYNC1H1):c.2868+37G>C
NM_001376.5(DYNC1H1):c.2869-248A>G
NM_001376.5(DYNC1H1):c.2869-47T>A
NM_001376.5(DYNC1H1):c.3015+18C>G
NM_001376.5(DYNC1H1):c.3015+283T>C
NM_001376.5(DYNC1H1):c.3016-142C>T
NM_001376.5(DYNC1H1):c.3333+23A>G
NM_001376.5(DYNC1H1):c.344+171C>T
NM_001376.5(DYNC1H1):c.345-49T>C
NM_001376.5(DYNC1H1):c.3565-108T>C
NM_001376.5(DYNC1H1):c.3565-322C>A
NM_001376.5(DYNC1H1):c.3805-148A>G
NM_001376.5(DYNC1H1):c.3805-73C>T
NM_001376.5(DYNC1H1):c.4075-276G>A
NM_001376.5(DYNC1H1):c.4075-6C>T rs377411812
NM_001376.5(DYNC1H1):c.409G>A (p.Val137Ile) rs143421325
NM_001376.5(DYNC1H1):c.4396-25A>G
NM_001376.5(DYNC1H1):c.4533G>A (p.Pro1511=) rs150900416
NM_001376.5(DYNC1H1):c.4542+232A>G
NM_001376.5(DYNC1H1):c.4884-280C>T
NM_001376.5(DYNC1H1):c.4884-93G>C
NM_001376.5(DYNC1H1):c.5298G>T (p.Leu1766=) rs149395439
NM_001376.5(DYNC1H1):c.5310C>T (p.Gly1770=) rs34013442
NM_001376.5(DYNC1H1):c.5716+294A>T
NM_001376.5(DYNC1H1):c.5818-229G>C
NM_001376.5(DYNC1H1):c.5970C>T (p.Tyr1990=)
NM_001376.5(DYNC1H1):c.5977+77G>A
NM_001376.5(DYNC1H1):c.6618+72G>A
NM_001376.5(DYNC1H1):c.6619-168G>A
NM_001376.5(DYNC1H1):c.6795C>T (p.Tyr2265=) rs200339812
NM_001376.5(DYNC1H1):c.7203A>C (p.Lys2401Asn) rs150888094
NM_001376.5(DYNC1H1):c.7290C>T (p.Asn2430=) rs112811548
NM_001376.5(DYNC1H1):c.8177+319_8177+320dup
NM_001376.5(DYNC1H1):c.8178-223T>C
NM_001376.5(DYNC1H1):c.8344-188G>A
NM_001376.5(DYNC1H1):c.8344-30G>A
NM_001376.5(DYNC1H1):c.8638-255A>G
NM_001376.5(DYNC1H1):c.8784A>G (p.Gln2928=) rs149753029
NM_001376.5(DYNC1H1):c.9468+108T>C
NM_001376.5(DYNC1H1):c.962-168G>A
NM_001376.5(DYNC1H1):c.9762+77C>A

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