List of variants in gene combination LOC129933707, MSH6 reported as uncertain significance for colorectal cancer

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: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.245C>T (p.Pro82Leu)	rs1190756871	0.00001
NM_000179.3(MSH6):c.247G>A (p.Ala83Thr)	rs755964436
NM_000179.3(MSH6):c.248C>A (p.Ala83Asp)	rs876661197
NM_000179.3(MSH6):c.248C>G (p.Ala83Gly)	rs876661197
NM_000179.3(MSH6):c.249T>G (p.Ala83=)	rs876658308
NM_000179.3(MSH6):c.251C>T (p.Ala84Val)	rs878853717
NM_000179.3(MSH6):c.253C>T (p.Pro85Ser)	rs779664343
NM_000179.3(MSH6):c.254C>T (p.Pro85Leu)	rs1060502945
NM_000179.3(MSH6):c.254CCA[1] (p.Thr86del)	rs1553408448
NM_000179.3(MSH6):c.259A>C (p.Ser87Arg)	rs1064793939
NM_000179.3(MSH6):c.260+4G>A	rs1389301978

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.