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ATM c.1651_1653delinsTAA ;(p.V551*)
Variant ID: 11-108122607-GTT-TAA
NM_000051.3(
ATM
):c.1651_1653delinsTAA;(p.V551*)
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Evaluation of ATM heterozygous mutations underlying individual differences in radiosensitivity using genome editing in human cultured cells.
Scientific Reports
Royba, Ekaterina E; Miyamoto, Tatsuo T; Natsuko Akutsu, Silvia S; Hosoba, Kosuke K; Tauchi, Hiroshi H; Kudo, Yoshiki Y; Tashiro, Satoshi S; Yamamoto, Takashi T; Matsuura, Shinya S
Publication Date: 2017-07-20
Variant appearance in text: ATM: V551X
PubMed Link:
28729543
Variant Present in the following documents:
Main text
41598_2017_Article_6393.pdf
41598_2017_6393_MOESM1_ESM.pdf
View BVdb publication page