List of variants in gene DYNC2H1 reported as likely benign by Illumina Laboratory Services, Illumina

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: 30

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HGVS	dbSNP	gnomAD frequency
NM_001377.3(DYNC2H1):c.8580A>G (p.Glu2860=)	rs17394217	0.10011
NM_001377.3(DYNC2H1):c.5558+4A>G	rs11225578	0.09042
NM_001377.3(DYNC2H1):c.1021C>T (p.His341Tyr)	rs17301182	0.08953
NM_001377.3(DYNC2H1):c.3862A>G (p.Thr1288Ala)	rs17301750	0.08745
NM_001377.3(DYNC2H1):c.12457-6C>T	rs11225812	0.07031
NM_001377.3(DYNC2H1):c.21C>T (p.Asp7=)	rs17301028	0.06536
NM_001377.3(DYNC2H1):c.911A>T (p.Gln304Leu)	rs12146610	0.04434
NM_001377.3(DYNC2H1):c.2454G>A (p.Glu818=)	rs77738279	0.03320
NM_001377.3(DYNC2H1):c.9353+7G>A	rs78309870	0.02821
NM_001377.3(DYNC2H1):c.1367G>A (p.Arg456Gln)	rs17099969	0.02244
NM_001377.3(DYNC2H1):c.2818+13T>C	rs150786504	0.01848
NM_001377.3(DYNC2H1):c.4068C>T (p.Phe1356=)	rs74713170	0.01817
NM_001377.3(DYNC2H1):c.10461A>G (p.Gln3487=)	rs75143468	0.01568
NM_001377.3(DYNC2H1):c.645A>G (p.Leu215=)	rs116666272	0.01563
NM_001377.3(DYNC2H1):c.7122G>A (p.Leu2374=)	rs116574613	0.01532
NM_001377.3(DYNC2H1):c.*265C>T	rs78537620	0.01499
NM_001377.3(DYNC2H1):c.1233A>G (p.Gln411=)	rs116888435	0.01403
NM_001377.3(DYNC2H1):c.-94G>T	rs114993913	0.01360
NM_001377.3(DYNC2H1):c.10479C>G (p.Leu3493=)	rs151056947	0.01253
NM_001377.3(DYNC2H1):c.2860G>A (p.Glu954Lys)	rs61898615	0.01194
NM_001377.3(DYNC2H1):c.6478-6C>T	rs114254215	0.01103
NM_001377.3(DYNC2H1):c.10834G>C (p.Asp3612His)	rs116872934	0.00628
NM_001377.3(DYNC2H1):c.9939T>C (p.Ala3313=)	rs192003811	0.00313
NM_001377.3(DYNC2H1):c.9814T>A (p.Leu3272Ile)	rs200342335	0.00219
NM_001377.3(DYNC2H1):c.9297T>C (p.Tyr3099=)	rs180787556	0.00212
NM_001377.3(DYNC2H1):c.4719A>G (p.Gln1573=)	rs201016942	0.00021
NM_001377.3(DYNC2H1):c.12457-13T>C	rs537890566	0.00019
NM_001377.3(DYNC2H1):c.5313A>G (p.Val1771=)	rs144553338	0.00016
NM_001377.3(DYNC2H1):c.7540+14G>A	rs115273161
NM_001377.3(DYNC2H1):c.7540+14G>T	rs115273161

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