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

Minimum submission review status:		Collection method:
Minimum conflict level:
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
NM_001377.3(DYNC2H1):c.*265C>T	rs78537620
NM_001377.3(DYNC2H1):c.-94G>T	rs114993913
NM_001377.3(DYNC2H1):c.1021C>T (p.His341Tyr)	rs17301182
NM_001377.3(DYNC2H1):c.10461A>G (p.Gln3487=)	rs75143468
NM_001377.3(DYNC2H1):c.10479C>G (p.Leu3493=)	rs151056947
NM_001377.3(DYNC2H1):c.10834G>C (p.Asp3612His)	rs116872934
NM_001377.3(DYNC2H1):c.1233A>G (p.Gln411=)	rs116888435
NM_001377.3(DYNC2H1):c.12457-13T>C	rs537890566
NM_001377.3(DYNC2H1):c.12457-6C>T	rs11225812
NM_001377.3(DYNC2H1):c.1367G>A (p.Arg456Gln)	rs17099969
NM_001377.3(DYNC2H1):c.21C>T (p.Asp7=)	rs17301028
NM_001377.3(DYNC2H1):c.2454G>A (p.Glu818=)	rs77738279
NM_001377.3(DYNC2H1):c.2818+13T>C	rs150786504
NM_001377.3(DYNC2H1):c.2860G>A (p.Glu954Lys)	rs61898615
NM_001377.3(DYNC2H1):c.3862A>G (p.Thr1288Ala)	rs17301750
NM_001377.3(DYNC2H1):c.4068C>T (p.Phe1356=)	rs74713170
NM_001377.3(DYNC2H1):c.4719A>G (p.Gln1573=)	rs201016942
NM_001377.3(DYNC2H1):c.5313A>G (p.Val1771=)	rs144553338
NM_001377.3(DYNC2H1):c.5558+4A>G	rs11225578
NM_001377.3(DYNC2H1):c.645A>G (p.Leu215=)	rs116666272
NM_001377.3(DYNC2H1):c.6478-6C>T	rs114254215
NM_001377.3(DYNC2H1):c.7122G>A (p.Leu2374=)	rs116574613
NM_001377.3(DYNC2H1):c.7540+14G>A	rs115273161
NM_001377.3(DYNC2H1):c.7540+14G>T
NM_001377.3(DYNC2H1):c.8580A>G (p.Glu2860=)	rs17394217
NM_001377.3(DYNC2H1):c.911A>T (p.Gln304Leu)	rs12146610
NM_001377.3(DYNC2H1):c.9297T>C (p.Tyr3099=)	rs180787556
NM_001377.3(DYNC2H1):c.9353+7G>A	rs78309870
NM_001377.3(DYNC2H1):c.9814T>A (p.Leu3272Ile)	rs200342335
NM_001377.3(DYNC2H1):c.9939T>C (p.Ala3313=)	rs192003811

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