Bibliome.ai browser hg19
Search
About
Stats
FAQ
ERBB2 c.1786T>A ;(p.C596S)
Variant ID: 17-37873621-T-A
NM_004448.2(
ERBB2
):c.1786T>A;(p.C596S)
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:
Identification of 22 Novel Motifs of the Cell Entry Fusion Glycoprotein B of Oncolytic Herpes Simplex Viruses: Sequence Analysis and Literature Review.
Frontiers In Oncology
Shi, Fang F; Xin, Victoria W VW; Liu, Xiao-Qin XQ; Wang, Ying-Ying YY; Zhang, Ying Y; Cheng, Jun-Ting JT; Cai, Wen-Qi WQ; Xiang, Ying Y; Peng, Xiao-Chun XC; Wang, Xianwang X; Xin, Hong-Wu HW
Publication Date: 2020
Variant appearance in text: HER2: C596S
PubMed Link:
32974139
Variant Present in the following documents:
Main text
fonc-10-01386.pdf
View BVdb publication page