MLH1 c.588+5G>C

Variant ID: 3-37053358-G-C

NM_000249.3(MLH1):c.588+5G>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Clinical and Molecular Characterization of Brazilian Patients Suspected to Have Lynch Syndrome.

Plos One
Carneiro da Silva, Felipe F; Ferreira, José Roberto de Oliveira JR; Torrezan, Giovana Tardin GT; Figueiredo, Márcia Cristina Pena MC; Santos, Érika Maria Monteiro ÉM; Nakagawa, Wilson Toshihiko WT; Brianese, Rafael Canfield RC; Petrolini de Oliveira, Ligia L; Begnani, Maria Dirlei MD; Aguiar-Junior, Samuel S; Rossi, Benedito Mauro BM; Ferreira, Fábio de Oliveira Fde O; Carraro, Dirce Maria DM
Publication Date: 2015

Variant appearance in text: MLH1: 588+5G>C
PubMed Link: 26437257
Variant Present in the following documents:
  • Main text
  • pone.0139753.pdf
View BVdb publication page