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