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ERBB2 c.26G>A ;(p.W9*)
Variant ID: 17-37856517-G-A
NM_004448.2(
ERBB2
):c.26G>A;(p.W9*)
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:
An entire exon 3 germ-line rearrangement in the BRCA2 gene: pathogenic relevance of exon 3 deletion in breast cancer predisposition.
Bmc Medical Genetics
Muller, Danièle D; Rouleau, Etienne E; Schultz, Inès I; Caputo, Sandrine S; Lefol, Cédrick C; Bièche, Ivan I; Caron, Olivier O; Noguès, Catherine C; Limacher, Jean Marc JM; Demange, Liliane L; Lidereau, Rosette R; Fricker, Jean Pierre JP; Abecassis, Joseph J
Publication Date: 2011-09-22
Variant appearance in text: HER2: 26G>A
PubMed Link:
21939546
Variant Present in the following documents:
Main text
1471-2350-12-121.pdf
View BVdb publication page