ClinVar Miner

List of variants in gene DYNC1H1 reported as benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 88
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HGVS dbSNP
NM_001376.5(DYNC1H1):c.10079+93C>G
NM_001376.5(DYNC1H1):c.10293C>T (p.Asn3431=) rs75075497
NM_001376.5(DYNC1H1):c.10413+93G>A
NM_001376.5(DYNC1H1):c.10950C>T (p.Asn3650=) rs17541505
NM_001376.5(DYNC1H1):c.11207-75del
NM_001376.5(DYNC1H1):c.11400G>A (p.Gln3800=) rs182767009
NM_001376.5(DYNC1H1):c.11409G>A (p.Pro3803=) rs17512783
NM_001376.5(DYNC1H1):c.11685C>T (p.Thr3895=) rs17541519
NM_001376.5(DYNC1H1):c.11690+239A>G
NM_001376.5(DYNC1H1):c.11765C>T (p.Pro3922Leu) rs141696238
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.12159A>T (p.Gly4053=) rs115992196
NM_001376.5(DYNC1H1):c.12192G>T (p.Thr4064=) rs114906811
NM_001376.5(DYNC1H1):c.12514-259G>C
NM_001376.5(DYNC1H1):c.12684+14A>G rs200392758
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.13373-273G>C
NM_001376.5(DYNC1H1):c.13516-16C>T rs28669726
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.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.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+18C>T rs2749894
NM_001376.5(DYNC1H1):c.3015+283T>C
NM_001376.5(DYNC1H1):c.3016-142C>T
NM_001376.5(DYNC1H1):c.306C>T (p.Asn102=) rs17540624
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.3600A>G (p.Gln1200=) rs12893215
NM_001376.5(DYNC1H1):c.3805-148A>G
NM_001376.5(DYNC1H1):c.3805-73C>T
NM_001376.5(DYNC1H1):c.3993C>T (p.Gly1331=) rs17540957
NM_001376.5(DYNC1H1):c.4075-276G>A
NM_001376.5(DYNC1H1):c.4185+20C>T rs74948967
NM_001376.5(DYNC1H1):c.4395+2C>T rs192594531
NM_001376.5(DYNC1H1):c.4396-25A>G
NM_001376.5(DYNC1H1):c.4515G>A (p.Ser1505=) rs186932188
NM_001376.5(DYNC1H1):c.4533G>A (p.Pro1511=) rs150900416
NM_001376.5(DYNC1H1):c.4542+232A>G
NM_001376.5(DYNC1H1):c.4854T>C (p.Tyr1618=) rs75094258
NM_001376.5(DYNC1H1):c.4884-280C>T
NM_001376.5(DYNC1H1):c.4884-93G>C
NM_001376.5(DYNC1H1):c.5433+17dup rs140185574
NM_001376.5(DYNC1H1):c.5716+294A>T
NM_001376.5(DYNC1H1):c.5818-229G>C
NM_001376.5(DYNC1H1):c.5977+77G>A
NM_001376.5(DYNC1H1):c.624G>A (p.Pro208=) rs3818188
NM_001376.5(DYNC1H1):c.6618+72G>A
NM_001376.5(DYNC1H1):c.6619-168G>A
NM_001376.5(DYNC1H1):c.7137G>A (p.Leu2379=) rs17512439
NM_001376.5(DYNC1H1):c.738A>G (p.Gln246=) rs117189734
NM_001376.5(DYNC1H1):c.7410G>A (p.Ala2470=) rs139109090
NM_001376.5(DYNC1H1):c.7449C>T (p.Ile2483=) rs17541158
NM_001376.5(DYNC1H1):c.7458G>T (p.Leu2486=) rs17541165
NM_001376.5(DYNC1H1):c.8177+319_8177+320dup
NM_001376.5(DYNC1H1):c.8178-223T>C
NM_001376.5(DYNC1H1):c.8304G>A (p.Pro2768=) rs77113510
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.8886+13G>A rs17541317
NM_001376.5(DYNC1H1):c.8928A>G (p.Leu2976=) rs8010870
NM_001376.5(DYNC1H1):c.9138G>T (p.Ser3046=) rs34338935
NM_001376.5(DYNC1H1):c.9264-8T>G rs368432468
NM_001376.5(DYNC1H1):c.9468+108T>C
NM_001376.5(DYNC1H1):c.962-15dup rs3830914
NM_001376.5(DYNC1H1):c.962-168G>A
NM_001376.5(DYNC1H1):c.9762+77C>A

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