MSH6 c.1707del ;(p.F569Lfs*2)

Variant ID: 2-48026829-TC-T

NM_000179.2(MSH6):c.1707del;(p.F569Lfs*2)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Comprehensive characterisation of pancreatic ductal adenocarcinoma with microsatellite instability: histology, molecular pathology and clinical implications.

Gut
Luchini, Claudio C; Brosens, Lodewijk A A LAA; Wood, Laura D LD; Chatterjee, Deyali D; Shin, Jae Il JI; Sciammarella, Concetta C; Fiadone, Giulia G; Malleo, Giuseppe G; Salvia, Roberto R; Kryklyva, Valentyna V; Piredda, Maria L ML; Cheng, Liang L; Lawlor, Rita T RT; Adsay, Volkan V; Scarpa, Aldo A
Publication Date: 2021-01

Variant appearance in text: MSH6: 1707delC
PubMed Link: 32350089
Variant Present in the following documents:
  • Main text
  • gutjnl-2020-320726.pdf
View BVdb publication page



Prevalence of germline mutations in cancer predisposition genes in patients with pancreatic cancer.

Gastroenterology
Grant, Robert C RC; Selander, Iris I; Connor, Ashton A AA; Selvarajah, Shamini S; Borgida, Ayelet A; Briollais, Laurent L; Petersen, Gloria M GM; Lerner-Ellis, Jordan J; Holter, Spring S; Gallinger, Steven S
Publication Date: 2015-03

Variant appearance in text: MSH6: 1707delC; F569fs
PubMed Link: 25479140
Variant Present in the following documents:
  • Main text
View BVdb publication page