ERBB2 c.1579C>T ;(p.Q527*)

Variant ID: 17-37872619-C-T

NM_004448.2(ERBB2):c.1579C>T;(p.Q527*)

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:

Analysis of the frequency of oncogenic driver mutations and correlation with clinicopathological characteristics in patients with lung adenocarcinoma from Northeastern Switzerland.

Diagnostic Pathology
Grosse, Alexandra A; Grosse, Claudia C; Rechsteiner, Markus M; Soltermann, Alex A
Publication Date: 2019-02-11

Variant appearance in text: ERBB2: 1579C>T; Gln527Ter
PubMed Link: 30744664
Variant Present in the following documents:
  • Main text
  • 13000_2019_Article_789.pdf
View BVdb publication page