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ATM c.8786+11T>C
Variant ID: 11-108224618-T-C
NM_000051.3(
ATM
):c.8786+11T>C
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:
Description and validation of high-throughput simultaneous genotyping and mutation scanning by high-resolution melting curve analysis.
Human Mutation
Nguyen-Dumont, TĂș T; Calvez-Kelm, Florence Le FL; Forey, Nathalie N; McKay-Chopin, Sandrine S; Garritano, Sonia S; Gioia-Patricola, Lydie L; De Silva, Deepika D; Weigel, Ron R; Sangrajrang, Suleeporn S; Lesueur, Fabienne F; Tavtigian, Sean V SV; , ; ,
Publication Date: 2009-06
Variant appearance in text: ATM: 8786+11T>C
PubMed Link:
19347964
Variant Present in the following documents:
Main text
View BVdb publication page