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ATM c.3968A>T ;(p.K1323I)
Variant ID: 11-108155175-A-T
NM_000051.3(
ATM
):c.3968A>T;(p.K1323I)
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:
Amplicon-Based NGS Panels for Actionable Cancer Target Identification in Follicular Cell-Derived Thyroid Neoplasia.
Frontiers In Endocrinology
Madsen, Majbritt Busk MB; Kiss, Katalin K; Cilius Nielsen, Finn F; Bennedbæk, Finn Noe FN; Rossing, Maria M
Publication Date: 2020
Variant appearance in text: ATM: 3968A>T; K1323I
PubMed Link:
32265839
Variant Present in the following documents:
Main text
fendo-11-00146.pdf
Table_1.pdf
View BVdb publication page