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ATM c.3944C>T ;(p.A1315V)
Variant ID: 11-108155151-C-T
NM_000051.3(
ATM
):c.3944C>T;(p.A1315V)
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:
Validity of an NGS-based multiple gene panel in identifying actionable mutations for patients with NSCLC in a Chinese hospital.
Oncology Letters
Cao, Wei W; Yan, Chenghai C; Wang, Hailong H; Tang, Tom T; Wang, Haifeng H; Liu, Dujuan D
Publication Date: 2019-06
Variant appearance in text: ATM: A1315V
PubMed Link:
31186761
Variant Present in the following documents:
Main text
ol-17-06-5425.pdf
View BVdb publication page
Comprehensive genomic analysis of Oesophageal Squamous Cell Carcinoma reveals clinical relevance.
Scientific Reports
Du, Peina P; Huang, Peide P; Huang, Xuanlin X; Li, Xiangchun X; Feng, Zhimin Z; Li, Fengyu F; Liang, Shaoguang S; Song, Yongmei Y; Stenvang, Jan J; BrĂ¼nner, Nils N; Yang, Huanming H; Ou, Yunwei Y; Gao, Qiang Q; Li, Lin L
Publication Date: 2017-11-10
Variant appearance in text: ATM: 3944C>T; A1315V
PubMed Link:
29127303
Variant Present in the following documents:
41598_2017_14909_MOESM4_ESM.xlsx, sheet 1
View BVdb publication page