MSH2 c.1582A>T ;(p.K528*)

Variant ID: 2-47693868-A-T

NM_000251.2(MSH2):c.1582A>T;(p.K528*)

This variant was identified in 2 publications

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Systematic assessment and optimizing algorithm of tumor mutational burden calculation and their implications in clinical decision-making.

Frontiers In Oncology
Sun, Daqiang D; Xu, Meilin M; Pan, Chaohu C; Tang, Hongzhen H; Wang, Peng P; Wu, Dongfang D; Luo, Haitao H
Publication Date: 2022

Variant appearance in text: MSH2: 1582A>T; Lys528Ter
PubMed Link: 36425562
Variant Present in the following documents:
  • Table_5.xlsx, sheet 1
  • Table_4.xlsx, sheet 1
  • Table_3.xlsx, sheet 1
View BVdb publication page


Insights into protein - DNA interactions, stability and allosteric communications: a computational study of mutSĪ±-DNA recognition complexes.

Journal Of Biomolecular Structure & Dynamics
Negureanu, Lacramioara L; Salsbury, Freddie R FR
Publication Date: 2012

Variant appearance in text: MSH2: Lys528*
PubMed Link: 22208277
Variant Present in the following documents:
  • Main text
View BVdb publication page