MSH2 c.34_36delinsTTT ;(p.E12F)

Variant ID: 2-47630364-GAG-TTT

NM_000251.2(MSH2):c.34_36delinsTTT;(p.E12F)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Single-amplicon MSH2 A636P mutation testing in Ashkenazi Jewish patients with colorectal cancer: role in presurgical management.

Annals Of Surgery
Guillem, Jose G JG; Glogowski, Emily E; Moore, Harvey G HG; Nafa, Khedoudja K; Markowitz, Arnold J AJ; Shia, Jinru J; Offit, Kenneth K; Ellis, Nathan A NA
Publication Date: 2007-04

Variant appearance in text: MSH2: E12F
PubMed Link: 17414604
Variant Present in the following documents:
  • Main text
View BVdb publication page