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POLE c.2656C>T ;(p.P886S)
Variant ID: 12-133240640-G-A
NM_006231.2(
POLE
):c.2656C>T;(p.P886S)
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:
Genomic Alterations of NTRK, POLE, ERBB2, and Microsatellite Instability Status in Chinese Patients with Colorectal Cancer.
The Oncologist
Guo, Yun Y; Guo, Xian-Ling XL; Wang, Shuang S; Chen, Xinyu X; Shi, Jiaochun J; Wang, Jian J; Wang, Kai K; Klempner, Samuel J SJ; Wang, Weifeng W; Xiao, Min M
Publication Date: 2020-11
Variant appearance in text: POLE: P886S
PubMed Link:
32627883
Variant Present in the following documents:
Main text
ONCO-25-e1671.pdf
View BVdb publication page