List of variants in gene combination CDK4, TSPAN31 reported as 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_005981.5(TSPAN31):c.*529C>T	rs184712	0.22296
NM_005981.5(TSPAN31):c.*798G>C	rs3472	0.03579
NM_005981.5(TSPAN31):c.*865A>C	rs3473	0.03562
NM_005981.5(TSPAN31):c.*714C>T	rs113625101	0.03374
NM_005981.5(TSPAN31):c.*744G>A	rs112275916	0.02614
NM_005981.5(TSPAN31):c.*1025C>T	rs2069511	0.00275
NM_005981.5(TSPAN31):c.*484G>A	rs192347082	0.00025
NM_005981.5(TSPAN31):c.*2031T>A	rs370609910	0.00016
NM_000075.4(CDK4):c.763C>T (p.Arg255Cys)	rs587778188	0.00002
NM_005981.5(TSPAN31):c.*2222G>A	rs536249985

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