MSH6 c.3678A>G ;(p.A1226=)

Variant ID: 2-48033374-A-G

NM_000179.2(MSH6):c.3678A>G;(p.A1226=)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Screening of the DNA mismatch repair genes MLH1, MSH2 and MSH6 in a Greek cohort of Lynch syndrome suspected families.

Bmc Cancer
Thodi, Georgia G; Fostira, Florentia F; Sandaltzopoulos, Raphael R; Nasioulas, George G; Grivas, Anastasios A; Boukovinas, Ioannis I; Mylonaki, Maria M; Panopoulos, Christos C; Magic, Mirjana Brankovic MB; Fountzilas, George G; Yannoukakos, Drakoulis D
Publication Date: 2010-10-11

Variant appearance in text: MSH6: 3678A>G; Ala1226Ala
PubMed Link: 20937110
Variant Present in the following documents:
  • Main text
  • 1471-2407-10-544.pdf
View BVdb publication page