List of variants in gene combination CDK4, TSPAN31 reported as likely benign by Quest Diagnostics Nichols Institute San Juan Capistrano

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000075.4(CDK4):c.776C>T (p.Ser259Leu)	rs201617914	0.00007
NM_000075.4(CDK4):c.661G>A (p.Asp221Asn)	rs587778187	0.00002
NM_000075.4(CDK4):c.660C>T (p.Ala220=)	rs773490152	0.00001
NM_000075.4(CDK4):c.798G>A (p.Glu266=)	rs780522588	0.00001
NM_005981.5(TSPAN31):c.*2037dup	rs757684130	0.00001
NM_000075.4(CDK4):c.752C>G (p.Pro251Arg)	rs143670820
NM_000075.4(CDK4):c.753C>A (p.Pro251=)	rs757333818

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