POLE c.37C>T ;(p.P13S)

Variant ID: 12-133263865-G-A

NM_006231.2(POLE):c.37C>T;(p.P13S)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Genetic variants in African-American and Hispanic patients with breast cancer.

Oncology Letters
Dutta, Pranabananda P; Keung, Man Y MY; Wu, Yanyuan Y; Vadgama, Jaydutt V JV
Publication Date: 2023-02

Variant appearance in text: POLE: 37C>T
PubMed Link: 36644153
Variant Present in the following documents:
  • Supplementary_Data5.xlsx, sheet 1
View BVdb publication page



Next-generation sequencing in thyroid cancers: do targetable alterations lead to a therapeutic advantage?: A multicenter experience.

Medicine
Moore, Assaf A; Bar, Yael Y; Maurice-Dror, Corinne C; Finkel, Inbar I; Goldvaser, Hadar H; Dudnik, Elizabeth E; Goldstein, Daniel A DA; Gordon, Noa N; Billan, Salem S; Gutfeld, Orit O; Wolf, Ido I; Popovtzer, Aron A
Publication Date: 2021-06-25

Variant appearance in text: POLE: P13S
PubMed Link: 34160418
Variant Present in the following documents:
  • medi-100-e26388.pdf
View BVdb publication page



Exome sequencing in 51 early onset non-familial CRC cases.

Molecular Genetics & Genomic Medicine
Thutkawkorapin, Jessada J; Lindblom, Annika A; Tham, Emma E
Publication Date: 2019-05

Variant appearance in text: POLE: 37C>T; Pro13Ser
PubMed Link: 30809968
Variant Present in the following documents:
  • Main text
  • MGG3-7-e605.pdf
View BVdb publication page