List of variants in gene MSH6 studied for Ovarian cancer

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 15

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.3674C>T (p.Thr1225Met)	rs63750370	0.00011
NM_000179.3(MSH6):c.926C>G (p.Ser309Cys)	rs544222338	0.00006
NM_000179.3(MSH6):c.107C>T (p.Ala36Val)	rs61756469	0.00004
NM_000179.3(MSH6):c.229C>T (p.Arg77Trp)	rs745442468	0.00003
NM_000179.3(MSH6):c.3244C>T (p.Pro1082Ser)	rs186240214	0.00002
NM_000179.3(MSH6):c.3819T>G (p.Asn1273Lys)	rs759642651	0.00001
NM_000179.3(MSH6):c.727C>T (p.Arg243Cys)	rs377216828	0.00001
NM_000179.3(MSH6):c.1085C>T (p.Pro362Leu)
NM_000179.3(MSH6):c.2156C>G (p.Thr719Ser)	rs373418713
NM_000179.3(MSH6):c.2422G>A (p.Val808Ile)	rs1434578765
NM_000179.3(MSH6):c.2636C>G (p.Ala879Gly)
NM_000179.3(MSH6):c.2899A>G (p.Ile967Val)	rs876661067
NM_000179.3(MSH6):c.3259C>A (p.Pro1087Thr)	rs63750998
NM_000179.3(MSH6):c.3259C>T (p.Pro1087Ser)	rs63750998
NM_000179.3(MSH6):c.3970G>C (p.Glu1324Gln)	rs540890590

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.