Varaico: Literature-Extracted Genetic Variants

Gene:MSH2
Variant:p.R468fs
Back to variants list

MSH2

NM_001258281.1:p.R468fs

Associated Papers

Comprehensive characterization of CRC with germline mutations reveals a distinct somatic mutational landscape and elevated cancer risk in the Chinese population.

Yao J et al.

Cancer Biology & Medicine, 2022

Germline and somatic mutations of homologous recombination-associated genes in Japanese ovarian cancer patients.

Sugino K et al.

Scientific Reports, 2019

Somatic mutations in MLH1 and MSH2 are a frequent cause of mismatch-repair deficiency in Lynch syndrome-like tumors.

Mensenkamp AR et al.

Gastroenterology, 2014

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."