MSH6 c.3982C>T ;(p.Q1328*)

Variant ID: 2-48033771-C-T

NM_000179.2(MSH6):c.3982C>T;(p.Q1328*)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Precision Oncology in Metastatic Uterine Cancer; Croatian First-Year Experience of the Comprehensive Genomic Profiling in Everyday Clinical Practice.

Pathology Oncology Research : Por
Čerina, Dora D; Matković, Višnja V; Katić, Kristina K; Lovasić, Ingrid Belac IB; Šeparović, Robert R; Canjko, Ivana I; Jakšić, Blanka B; Fröbe, Ana A; Pleština, Stjepko S; Bajić, Žarko Ž; Vrdoljak, Eduard E
Publication Date: 2021

Variant appearance in text: MSH6: Q1328*
PubMed Link: 34646088
Variant Present in the following documents:
  • DataSheet3.xlsx, sheet 1
  • DataSheet4.xlsx, sheet 1
View BVdb publication page



Distinctive DNA mismatch repair and APC rare variants in African Americans with colorectal neoplasia.

Oncotarget
Ashktorab, Hassan H; Azimi, Hamed H; Varma, Sudhir S; Tavakoli, Payaam P; Nickerson, Michael L ML; Brim, Hassan H
Publication Date: 2017-11-21

Variant appearance in text: MSH6: Q1328X
PubMed Link: 29245953
Variant Present in the following documents:
  • oncotarget-08-99966-s003.xlsx, sheet 2
View BVdb publication page



Molecular genetic analysis of 103 sporadic colorectal tumours in Czech patients.

Plos One
Vasovcak, Peter P; Pavlikova, Kristyna K; Sedlacek, Zdenek Z; Skapa, Petr P; Kouda, Martin M; Hoch, Jiri J; Krepelova, Anna A
Publication Date: 2011

Variant appearance in text: MSH6: 3982C>T; Q1328X
PubMed Link: 21901162
Variant Present in the following documents:
  • pone.0024114.s001.xls, sheet 1
View BVdb publication page