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ERBB2 c.2896_2898delinsTGT ;(p.R966C)
Variant ID: 17-37882838-CGG-TGT
NM_004448.2(
ERBB2
):c.2896_2898delinsTGT;(p.R966C)
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 somatic mutations across the kinome reveals loss-of-function mutations in multiple cancer types.
Scientific Reports
Kumar, Runjun D RD; Bose, Ron R
Publication Date: 2017-07-25
Variant appearance in text: HER2: R966C
PubMed Link:
28743916
Variant Present in the following documents:
Main text
41598_2017_6366_MOESM5_ESM.xls, sheet 3
41598_2017_Article_6366.pdf
View BVdb publication page