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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 43

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HGVS	dbSNP	gnomAD frequency
NM_001377.3(DYNC2H1):c.6420T>C (p.Asn2140=)	rs11225584	0.10418
NM_001377.3(DYNC2H1):c.12457-6C>T	rs11225812	0.07031
NM_001377.3(DYNC2H1):c.911A>T (p.Gln304Leu)	rs12146610	0.04434
NM_001377.3(DYNC2H1):c.9353+7G>A	rs78309870	0.02821
NM_001377.3(DYNC2H1):c.4728C>G (p.Asn1576Lys)	rs72989738	0.02353
NM_001377.3(DYNC2H1):c.1367G>A (p.Arg456Gln)	rs17099969	0.02244
NM_001377.3(DYNC2H1):c.4068C>T (p.Phe1356=)	rs74713170	0.01817
NM_001377.3(DYNC2H1):c.2818+13T>C	rs150786504	0.01790
NM_001377.3(DYNC2H1):c.645A>G (p.Leu215=)	rs116666272	0.01688
NM_001377.3(DYNC2H1):c.3660T>C (p.Pro1220=)	rs118191062	0.01583
NM_001377.3(DYNC2H1):c.10327-53A>G	rs116174151	0.01569
NM_001377.3(DYNC2H1):c.10461A>G (p.Gln3487=)	rs75143468	0.01568
NM_001377.3(DYNC2H1):c.7122G>A (p.Leu2374=)	rs116574613	0.01532
NM_001377.3(DYNC2H1):c.1233A>G (p.Gln411=)	rs116888435	0.01403
NM_001377.3(DYNC2H1):c.10479C>G (p.Leu3493=)	rs151056947	0.01339
NM_001377.3(DYNC2H1):c.195+7T>C	rs112718117	0.01205
NM_001377.3(DYNC2H1):c.2860G>A (p.Glu954Lys)	rs61898615	0.01194
NM_001377.3(DYNC2H1):c.12865G>C (p.Gly4289Arg)	rs144717489	0.01113
NM_001377.3(DYNC2H1):c.6478-6C>T	rs114254215	0.01103
NM_001377.3(DYNC2H1):c.4968+18G>A	rs144263658	0.00894
NM_001377.3(DYNC2H1):c.1485+19G>A	rs111375449	0.00764
NM_001377.3(DYNC2H1):c.12254G>A (p.Arg4085His)	rs115480556	0.00689
NM_001377.3(DYNC2H1):c.10864C>A (p.Arg3622=)	rs117178504	0.00672
NM_001377.3(DYNC2H1):c.7198A>G (p.Ile2400Val)	rs114292876	0.00632
NM_001377.3(DYNC2H1):c.10834G>C (p.Asp3612His)	rs116872934	0.00628
NM_001377.3(DYNC2H1):c.12007G>A (p.Ala4003Thr)	rs61737514	0.00612
NM_001377.3(DYNC2H1):c.11703C>T (p.Asn3901=)	rs144624858	0.00606
NM_001377.3(DYNC2H1):c.10966A>G (p.Met3656Val)	rs151156076	0.00599
NM_001377.3(DYNC2H1):c.27G>T (p.Arg9=)	rs113537035	0.00594
NM_001377.3(DYNC2H1):c.11238C>T (p.Ser3746=)	rs78599571	0.00555
NM_001377.3(DYNC2H1):c.3097-4A>G	rs368802969	0.00476
NM_001377.3(DYNC2H1):c.5442C>T (p.Pro1814=)	rs76833922	0.00476
NM_001377.3(DYNC2H1):c.6477+14A>T	rs111970770	0.00460
NM_001377.3(DYNC2H1):c.1263C>A (p.Phe421Leu)	rs142881106	0.00365
NM_001377.3(DYNC2H1):c.3012T>C (p.Gly1004=)	rs202082545	0.00344
NM_001377.3(DYNC2H1):c.9939T>C (p.Ala3313=)	rs192003811	0.00327
NM_001377.3(DYNC2H1):c.9297T>C (p.Tyr3099=)	rs180787556	0.00212
NM_001377.3(DYNC2H1):c.7128A>G (p.Ala2376=)	rs371410128	0.00193
NM_001377.3(DYNC2H1):c.6478-17C>T	rs61899765	0.00172
NM_001377.3(DYNC2H1):c.1661+16T>C	rs187129481	0.00164
NM_001377.3(DYNC2H1):c.12566+17A>G	rs187787132	0.00113
NM_001377.3(DYNC2H1):c.7143A>G (p.Val2381=)	rs79832792	0.00057
NM_001377.3(DYNC2H1):c.7540+14G>A	rs115273161

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