MSH6 c.715A>T ;(p.R239W)

Variant ID: 2-48025837-A-T

NM_000179.2(MSH6):c.715A>T;(p.R239W)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Collaborative Group of the Americas on Inherited Gastrointestinal Cancers (CGA-IGC) Annual Virtual Meeting, November 13-15, 2021.

Familial Cancer
Publication Date: 2022-10

Variant appearance in text: MSH6: Arg239Trp
PubMed Link: 35366121
Variant Present in the following documents:
  • Main text
  • 10689_2021_Article_284.pdf
View BVdb publication page