MSH6 c.886G>T ;(p.V296F)

Variant ID: 2-48026008-G-T

NM_000179.2(MSH6):c.886G>T;(p.V296F)

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:

Rates of Variants of Uncertain Significance Among Patients With Breast Cancer Undergoing Genetic Testing: Regional Perspectives.

Frontiers In Oncology
Abdel-Razeq, Hikmat H; Tamimi, Faris F; Abujamous, Lama L; Abdel-Razeq, Rashid R; Abunasser, Mahmoud M; Edaily, Sara S; Abdulelah, Hazem H; Khashabeh, Razan Abu RA; Bater, Rayan R
Publication Date: 2022

Variant appearance in text: MSH6: 886G>T
PubMed Link: 35402282
Variant Present in the following documents:
  • fonc-12-673094.pdf
View BVdb publication page