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ATM c.2650C>G ;(p.P884A)
Variant ID: 11-108139148-C-G
NM_000051.3(
ATM
):c.2650C>G;(p.P884A)
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:
Comprehensive germline and somatic genomic profiles of Chinese patients with biliary tract cancer.
Frontiers In Oncology
Yu, Haipeng H; Xu, Yan Y; Gao, Wei W; Li, Mei M; He, Ji'an J; Deng, Xiaoqian X; Xing, Wenge W
Publication Date: 2022
Variant appearance in text: ATM: P884A
PubMed Link:
36072793
Variant Present in the following documents:
Table_3.xlsx, sheet 1
View BVdb publication page
Genetic Analysis of Archived Tumor Specimens for Hereditary Colorectal Cancer Syndromes in the Cajuns of Louisiana, a US Founder Population.
Clinical And Translational Gastroenterology
Karlitz, Jordan J JJ; Phillips, Amanda A; Sorrells, Kelly S KS; Rao, Shanti S
Publication Date: 2021-09-21
Variant appearance in text: ATM: Pro884Ala
PubMed Link:
34545850
Variant Present in the following documents:
Main text
ct9-12-e00392.pdf
View BVdb publication page