MLH1 c.1230del ;(p.I411Lfs*80)

Variant ID: 3-37067317-GC-G

NM_000249.3(MLH1):c.1230del;(p.I411Lfs*80)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Massive parallel sequencing in individuals with multiple primary tumours reveals the benefit of re-analysis.

Hereditary Cancer In Clinical Practice
Wallander, Karin K; Thonberg, HÃ¥kan H; Nilsson, Daniel D; Tham, Emma E
Publication Date: 2021-10-28

Variant appearance in text: MLH1: 1229delC
PubMed Link: 34711244
Variant Present in the following documents:
  • Main text
  • 13053_2021_Article_203.pdf
View BVdb publication page