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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