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ERBB2 c.2029_2031delinsTGG ;(p.R677W)
Variant ID: 17-37879654-CGA-TGG
NM_004448.2(
ERBB2
):c.2029_2031delinsTGG;(p.R677W)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Whole-genome sequencing of recurrent neuroblastoma reveals somatic mutations that affect key players in cancer progression and telomere maintenance.
Scientific Reports
Fransson, Susanne S; Martinez-Monleon, Angela A; Johansson, Mathias M; Sjöberg, Rose-Marie RM; Björklund, Caroline C; Ljungman, Gustaf G; Ek, Torben T; Kogner, Per P; Martinsson, Tommy T
Publication Date: 2020-12-31
Variant appearance in text: ERBB2: R677W
PubMed Link:
33384420
Variant Present in the following documents:
41598_2020_Article_78370.pdf
View BVdb publication page
DiMeX: A Text Mining System for Mutation-Disease Association Extraction.
Plos One
Mahmood, A S M Ashique AS; Wu, Tsung-Jung TJ; Mazumder, Raja R; Vijay-Shanker, K K
Publication Date: 2016
Variant appearance in text: HER2: Arg677Trp
PubMed Link:
27073839
Variant Present in the following documents:
pone.0152725.s003.xlsx, sheet 1
View BVdb publication page