List of variants in gene XPC reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 18

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_004628.5(XPC):c.1443G>T (p.Lys481Asn)	rs182616621	0.00456
NM_004628.5(XPC):c.1497G>A (p.Ala499=)	rs150344169	0.00123
NM_004628.5(XPC):c.2496T>C (p.Ile832=)	rs201597537	0.00083
NM_004628.5(XPC):c.1812C>T (p.Ala604=)	rs756484727	0.00057
NM_004628.5(XPC):c.1509C>T (p.Ser503=)	rs760867012	0.00009
NM_004628.5(XPC):c.2688G>A (p.Ala896=)	rs368832210	0.00009
NM_004628.5(XPC):c.1725C>T (p.Asp575=)	rs377666880	0.00006
NM_004628.5(XPC):c.2331C>A (p.Pro777=)	rs769819782	0.00005
NM_004628.5(XPC):c.1616A>G (p.Glu539Gly)	rs563236303	0.00004
NM_004628.5(XPC):c.2418C>T (p.Pro806=)	rs199828421	0.00004
NM_004628.5(XPC):c.2043G>A (p.Val681=)	rs756438962	0.00003
NM_004628.5(XPC):c.1131C>T (p.Cys377=)	rs187340581	0.00002
NM_004628.5(XPC):c.1983C>T (p.Pro661=)	rs1255758517	0.00001
NM_004628.5(XPC):c.900T>C (p.His300=)	rs929649978	0.00001
NM_004628.5(XPC):c.1000C>T (p.Pro334Ser)	rs200338014
NM_004628.5(XPC):c.216A>G (p.Lys72=)	rs2125046003
NM_004628.5(XPC):c.2748G>A (p.Leu916=)
NM_004628.5(XPC):c.878G>A (p.Arg293Gln)

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.