MLH1 c.1744_1746del ;(p.L582del)

Variant ID: 3-37089022-GCTC-G

NM_000249.3(MLH1):c.1744_1746del;(p.L582del)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Robust diagnostic genetic testing using solution capture enrichment and a novel variant-filtering interface.

Human Mutation
Watson, Christopher M CM; Crinnion, Laura A LA; Morgan, Joanne E JE; Harrison, Sally M SM; Diggle, Christine P CP; Adlard, Julian J; Lindsay, Helen A HA; Camm, Nick N; Charlton, Ruth R; Sheridan, Eamonn E; Bonthron, David T DT; Taylor, Graham R GR; Carr, Ian M IM
Publication Date: 2014-04

Variant appearance in text: MLH1: 1744_1746del; Leu582del
PubMed Link: 24307375
Variant Present in the following documents:
  • Main text
  • humu0035-0434.pdf
View BVdb publication page