MSH6 c.688G>T ;(p.E230*)

Variant ID: 2-48025810-G-T

NM_000179.2(MSH6):c.688G>T;(p.E230*)

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:

Next generation sequencing to decipher concurrent loss of PMS2 and MSH6 in colorectal cancer.

Diagnostic Pathology
Moreno, Esther E; Rosa-Rosa, Juan M JM; Caniego-Casas, Tamara T; Ruz-Caracuel, Ignacio I; Perna, Cristian C; Guillén, Carmen C; Palacios, José J
Publication Date: 2020-07-14

Variant appearance in text: MSH6: E230*
PubMed Link: 32664968
Variant Present in the following documents:
  • Main text
  • 13000_2020_Article_1001.pdf
View BVdb publication page