MSH6 c.893G>C ;(p.R298P)

Variant ID: 2-48026015-G-C

NM_000179.2(MSH6):c.893G>C;(p.R298P)

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:

The potential role of methyltransferase-like 5 in deficient mismatch repair of uterine corpus endometrial carcinoma.

Bioengineered
Liu, Xiaojuan X; Ma, Hui H; Ma, Lisha L; Li, Kun K; Kang, Yanhua Y
Publication Date: 2022-03

Variant appearance in text: MSH6: R298P
PubMed Link: 35166644
Variant Present in the following documents:
  • Main text
  • KBIE_13_2036912.pdf
View BVdb publication page