List of variants in gene ERCC3 reported as not provided

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_000122.2(ERCC3):c.2111C>T (p.Ser704Leu)	rs4150521	0.00227
NM_000122.2(ERCC3):c.847C>T (p.Arg283Cys)	rs145201970	0.00146
NM_000122.2(ERCC3):c.2182G>A (p.Val728Met)	rs143140054	0.00011
NM_000122.2(ERCC3):c.1421dup (p.Asp474fs)	rs587778281	0.00006
NM_000122.2(ERCC3):c.350A>G (p.Lys117Arg)	rs1805161	0.00004
NM_000122.2(ERCC3):c.1333A>T (p.Thr445Ser)	rs587778280	0.00003
NM_000122.2(ERCC3):c.2303C>T (p.Ala768Val)	rs372094432	0.00003
NM_000122.2(ERCC3):c.1996G>A (p.Asp666Asn)	rs587778275	0.00001
NM_000122.2(ERCC3):c.172G>A (p.Ala58Thr)	rs587778277
NM_000122.2(ERCC3):c.1960G>A (p.Glu654Lys)	rs568193912
NM_000122.2(ERCC3):c.2207G>T (p.Arg736Ile)	rs587778276
NM_000122.2(ERCC3):c.307A>G (p.Ile103Val)	rs587778278
NM_000122.2(ERCC3):c.657+6T>C
NM_000122.2(ERCC3):c.682G>C (p.Gly228Arg)	rs587778279

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.