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ATM c.1657G>T ;(p.G553*)
Variant ID: 11-108122613-G-T
NM_000051.3(
ATM
):c.1657G>T;(p.G553*)
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:
Sequencing of Lynch syndrome tumors reveals the importance of epigenetic alterations.
Oncotarget
Porkka, Noora N; Valo, Satu S; Nieminen, Taina T TT; Olkinuora, Alisa A; Mäki-Nevala, Satu S; Eldfors, Samuli S; Peltomäki, Päivi P
Publication Date: 2017-12-08
Variant appearance in text: ATM: G553*
PubMed Link:
29296220
Variant Present in the following documents:
oncotarget-08-108020-s006.xlsx, sheet 1
View BVdb publication page
Genome profile in a extremely rare case of pulmonary sclerosing pneumocytoma presenting with diffusely-scattered nodules in the right lung.
Cancer Biology & Therapy
Fan, Xiangshan X; Lin, Ling L; Wang, Jianjun J; Wang, Yu Y; Feng, Anning A; Nie, Ling L; Wu, Hongyan H; Meng, Fanqing F; Xu, Haodong H
Publication Date: 2018-01-02
Variant appearance in text: ATM: G553X
PubMed Link:
29236566
Variant Present in the following documents:
Main text
View BVdb publication page