List of variants in gene CDKN2A reported as uncertain significance by Department of Pathology and Laboratory Medicine, Sinai Health System

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: 14

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000077.5(CDKN2A):c.150+1104C>A	rs756102261	0.00069
NM_000077.5(CDKN2A):c.318G>A (p.Val106=)	rs199888003	0.00026
NM_000077.5(CDKN2A):c.206A>G (p.Glu69Gly)	rs372670098	0.00003
NM_000077.5(CDKN2A):c.343G>T (p.Val115Leu)	rs779913365	0.00002
NM_000077.5(CDKN2A):c.127A>G (p.Ser43Gly)	rs766854048	0.00001
NM_000077.5(CDKN2A):c.241C>T (p.Pro81Ser)	rs1334828764	0.00001
NM_000077.5(CDKN2A):c.352G>A (p.Ala118Thr)	rs1554653960	0.00001
NM_000077.5(CDKN2A):c.415G>C (p.Gly139Arg)	rs587781733	0.00001
NC_000009.11:g.21971207_21994139dup
NM_000077.5(CDKN2A):c.143C>A (p.Pro48Gln)	rs763804037
NM_000077.5(CDKN2A):c.170C>T (p.Ala57Val)	rs372266620
NM_000077.5(CDKN2A):c.249C>A (p.His83Gln)	rs34968276
NM_000077.5(CDKN2A):c.370C>T (p.Arg124Cys)	rs34170727
NM_058195.4(CDKN2A):c.193+6A>T	rs2131147918

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.