MLH1 c.19G>T ;(p.V7F)

Variant ID: 3-37035057-G-T

NM_000249.3(MLH1):c.19G>T;(p.V7F)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


A computational and structural analysis of germline and somatic variants affecting the DDR mechanism, and their impact on human diseases.

Scientific Reports
Magraner-Pardo, Lorena L; Laskowski, Roman A RA; Pons, Tirso T; Thornton, Janet M JM
Publication Date: 2021-07-12

Variant appearance in text: MLH1: 19G>T; Val7Phe; rs730881746
PubMed Link: 34253785
Variant Present in the following documents:
  • 41598_2021_93715_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page



Comparison of Molecular, Clinicopathological, and Pedigree Differences Between Lynch-Like and Lynch Syndromes.

Frontiers In Genetics
Xu, Yun Y; Huang, Zonghao Z; Li, Cong C; Zhu, Congcong C; Zhang, Yuqin Y; Guo, Tian'an T; Liu, Fangqi F; Xu, Ye Y
Publication Date: 2020

Variant appearance in text: MLH1: Val7Phe
PubMed Link: 32973888
Variant Present in the following documents:
  • Main text
  • fgene-11-00991.pdf
View BVdb publication page