MSH6 c.3261C>A ;(p.P1087=)

Variant ID: 2-48030647-C-A

NM_000179.2(MSH6):c.3261C>A;(p.P1087=)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Germline MSH6 mutations are more prevalent in endometrial cancer patient cohorts than hereditary non polyposis colorectal cancer cohorts.

The Ulster Medical Journal
Devlin, Lisa A LA; Graham, Colin A CA; Price, John H JH; Morrison, Patrick J PJ
Publication Date: 2008-01

Variant appearance in text: MSH6: Pro1087Pro
PubMed Link: 18269114
Variant Present in the following documents:
  • Main text
  • umj7701-025.pdf
View BVdb publication page