MSH6 c.770dup ;(p.D257Efs*6)

Variant ID: 2-48025891-G-GA

NM_000179.2(MSH6):c.770dup;(p.D257Efs*6)

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 contribution of Lynch syndrome to early onset malignancy in Ireland.

Bmc Cancer
Talbot, Alice A; O'Donovan, Emily E; Berkley, Eileen E; Nolan, Carmel C; Clarke, Roisin R; Gallagher, David D
Publication Date: 2021-05-26

Variant appearance in text: MSH6: 770dupA; Asp257GlufsX6
PubMed Link: 34039291
Variant Present in the following documents:
  • Main text
  • 12885_2021_Article_8263.pdf
View BVdb publication page