Bibliome.ai browser hg19
Search
About
Stats
FAQ
ATM c.1699A>G ;(p.N567D)
Variant ID: 11-108122655-A-G
NM_000051.3(
ATM
):c.1699A>G;(p.N567D)
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:
A sharp Pif1-dependent threshold separates DNA double-strand breaks from critically short telomeres.
Elife
Strecker, Jonathan J; Stinus, Sonia S; Caballero, Mariana Pliego MP; Szilard, Rachel K RK; Chang, Michael M; Durocher, Daniel D
Publication Date: 2017-08-03
Variant appearance in text: TEL1: N567D
PubMed Link:
28826474
Variant Present in the following documents:
Main text
elife-23783.pdf
View BVdb publication page