List of variants in gene PCARE reported as benign by Eurofins NTD LLC (GA)

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: 16

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001029883.3(PCARE):c.2112T>C (p.Asn704=)	rs10200693	0.30236
NM_001029883.3(PCARE):c.2374C>G (p.Leu792Val)	rs17744093	0.15871
NM_001029883.3(PCARE):c.2499G>A (p.Pro833=)	rs34253433	0.15556
NM_001029883.3(PCARE):c.3668+14T>C	rs72861052	0.06996
NM_001029883.3(PCARE):c.2889C>T (p.Ser963=)	rs144569618	0.02252
NM_001029883.3(PCARE):c.1844T>A (p.Val615Asp)	rs140776870	0.01391
NM_001029883.3(PCARE):c.3291G>A (p.Gln1097=)	rs183536545	0.01287
NM_001029883.3(PCARE):c.2063G>A (p.Cys688Tyr)	rs149601594	0.00556
NM_001029883.3(PCARE):c.3789G>A (p.Leu1263=)	rs199689791	0.00417
NM_001029883.3(PCARE):c.3739G>A (p.Gly1247Ser)	rs187333111	0.00365
NM_001029883.3(PCARE):c.184C>G (p.Pro62Ala)	rs76346220	0.00267
NM_001029883.3(PCARE):c.2875G>A (p.Ala959Thr)	rs192350796	0.00140
NM_001029883.3(PCARE):c.1882G>A (p.Ala628Thr)	rs571059484	0.00001
NM_001029883.3(PCARE):c.3058_3059delinsAG (p.Gln1020Arg)	rs796065322
NM_001029883.3(PCARE):c.3264_3266del (p.Pro1089del)	rs138020654
NM_001029883.3(PCARE):c.3673_3675dupAGC

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.