ERBB2 c.592_593delinsTA ;(p.M198*)

Variant ID: 17-37866083-AT-TA

NM_004448.2(ERBB2):c.592_593delinsTA;(p.M198*)

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:

Direct resequencing of the complete ERBB2 coding sequence reveals an absence of activating mutations in ERBB2 amplified breast cancer.

Genes, Chromosomes & Cancer
Zito, Christina I CI; Riches, David D; Kolmakova, Julia J; Simons, Jan J; Egholm, Michael M; Stern, David F DF
Publication Date: 2008-07

Variant appearance in text: ERBB2: M198X
PubMed Link: 18418848
Variant Present in the following documents:
  • Main text
View BVdb publication page