ERBB2 c.207C>T ;(p.A69=)

Variant ID: 17-37863376-C-T

NM_004448.2(ERBB2):c.207C>T;(p.A69=)

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 17-gene expression-based prognostic signature associated with the prognosis of patients with breast cancer: A STROBE-compliant study.

Medicine
Qian, Jin-Xian JX; Yu, Min M; Sun, Zhe Z; Jiang, Ai-Mei AM; Long, Bo B
Publication Date: 2020-04

Variant appearance in text: HER2: A69A
PubMed Link: 32282693
Variant Present in the following documents:
  • Main text
View BVdb publication page