MSH6 c.1126G>T ;(p.E376*)

Variant ID: 2-48026248-G-T

NM_000179.2(MSH6):c.1126G>T;(p.E376*)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Germline mismatch repair gene variants analyzed by universal sequencing in Japanese cancer patients.

Cancer Medicine
Kiyozumi, Yoshimi Y; Matsubayashi, Hiroyuki H; Horiuchi, Yasue Y; Higashigawa, Satomi S; Oishi, Takuma T; Abe, Masato M; Ohnami, Sumiko S; Urakami, Kenichi K; Nagashima, Takeshi T; Kusuhara, Masatoshi M; Miyake, Hidehiko H; Yamaguchi, Ken K
Publication Date: 2019-09

Variant appearance in text: MSH6: 1126G>T; Glu376*
PubMed Link: 31386297
Variant Present in the following documents:
  • Main text
  • CAM4-8-5534.pdf
  • CAM4-8-5534-s001.xlsx, sheet 1
View BVdb publication page