POLE c.5828C>T ;(p.A1943V)

Variant ID: 12-133210948-G-A

NM_006231.2(POLE):c.5828C>T;(p.A1943V)

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:

Whole-exome sequencing identifies prognostic mutational signatures in gastric cancer.

Annals Of Translational Medicine
Zhu, Zhenxin Z; Fu, Hongbing H; Wang, Shengzhou S; Yu, Xinxin X; You, Qing Q; Shi, Mengyao M; Dai, Chun C; Wang, Guan G; Cha, Wei W; Wang, Weimin W
Publication Date: 2020-11

Variant appearance in text: POLE: A1943V
PubMed Link: 33313229
Variant Present in the following documents:
  • Main text
  • atm-08-22-1484.pdf
View BVdb publication page