MLH1 c.1689A>G ;(p.I563M)

Variant ID: 3-37083780-A-G

NM_000249.3(MLH1):c.1689A>G;(p.I563M)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


The association between genetic variants in hMLH1 and hMSH2 and the development of sporadic colorectal cancer in the Danish population.

Bmc Medical Genetics
Christensen, Lise Lotte LL; Madsen, Bo E BE; Wikman, Friedrik P FP; Wiuf, Carsten C; Koed, Karen K; Tjønneland, Anne A; Olsen, Anja A; Syvänen, Ann-Christine AC; Andersen, Claus L CL; Orntoft, Torben F TF
Publication Date: 2008-06-11

Variant appearance in text: MLH1: 1689A>G; Ile563Met
PubMed Link: 18547406
Variant Present in the following documents:
  • Main text
  • 1471-2350-9-52.pdf
View BVdb publication page