List of variants in gene ERCC1 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: 8

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001983.4(ERCC1):c.843+357C>T	rs104894988	0.00189
NM_001983.4(ERCC1):c.322-123G>A	rs104894991	0.00022
NM_001983.4(ERCC1):c.106-73A>G	rs104894992	0.00014
NM_001983.4(ERCC1):c.426-11G>A	rs104894990	0.00003
NM_001983.4(ERCC1):c.106-83G>A	rs104894993
NM_001983.4(ERCC1):c.676A>T (p.Lys226Ter)	rs886039224
NM_001983.4(ERCC1):c.693C>G (p.Phe231Leu)	rs121913028
NM_001983.4(ERCC1):c.774+64C>T	rs104894989

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.