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.




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