List of variants in gene CCND2 reported by GeneReviews

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 7

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001759.4(CCND2):c.841C>T (p.Pro281Ser)	rs587777621	0.00001
NM_001759.4(CCND2):c.842C>T (p.Pro281Leu)	rs587777622	0.00001
NM_001759.4(CCND2):c.851T>G (p.Val284Gly)	rs777786993	0.00001
NM_001759.4(CCND2):c.808A>T (p.Lys270Ter)	rs587777619
NM_001759.4(CCND2):c.838A>G (p.Thr280Ala)	rs587777618
NM_001759.4(CCND2):c.839C>A (p.Thr280Asn)	rs587777620
NM_001759.4(CCND2):c.842C>G (p.Pro281Arg)	rs587777622

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.