ERBB2 c.1586T>C ;(p.V529A)

Variant ID: 17-37872626-T-C

NM_004448.2(ERBB2):c.1586T>C;(p.V529A)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Complex Landscape of Germline Variants in Brazilian Patients With Hereditary and Early Onset Breast Cancer.

Frontiers In Genetics
Torrezan, Giovana T GT; de Almeida, Fernanda G Dos Santos R FGDSR; Figueiredo, Márcia C P MCP; Barros, Bruna D de Figueiredo BDF; de Paula, Cláudia A A CAA; Valieris, Renan R; de Souza, Jorge E S JES; Ramalho, Rodrigo F RF; da Silva, Felipe C C FCC; Ferreira, Elisa N EN; de Nóbrega, Amanda F AF; Felicio, Paula S PS; Achatz, Maria I MI; de Souza, Sandro J SJ; Palmero, Edenir I EI; Carraro, Dirce M DM
Publication Date: 2018

Variant appearance in text: ERBB2: 1586T>C; Val529Ala
PubMed Link: 29868112
Variant Present in the following documents:
  • Main text
View BVdb publication page