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EGFR c.865G>C ;(p.A289P)
Variant ID: 7-55221821-G-C
NM_005228.3(
EGFR
):c.865G>C;(p.A289P)
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:
Integrative analysis prioritised oxytocin-related biomarkers associated with the aetiology of autism spectrum disorder.
Ebiomedicine
Wang, Tao T; Zhao, Tingting T; Liu, Liqiu L; Teng, Huajing H; Fan, Tianda T; Li, Yi Y; Wang, Yan Y; Li, Jinchen J; Xia, Kun K; Sun, Zhongsheng Z
Publication Date: 2022-07
Variant appearance in text: EGFR: 865G>C; A289P
PubMed Link:
35665681
Variant Present in the following documents:
mmc26.xlsx, sheet 1
View BVdb publication page
Mutational profiling of kinases in human tumours of pancreatic origin identifies candidate cancer genes in ductal and ampulla of vater carcinomas.
Plos One
Corbo, Vincenzo V; Ritelli, Rossana R; Barbi, Stefano S; Funel, Niccola N; Campani, Daniela D; Bardelli, Alberto A; Scarpa, Aldo A
Publication Date: 2010-09-08
Variant appearance in text: EGFR: 865G>C
PubMed Link:
20838624
Variant Present in the following documents:
Main text
View BVdb publication page