ERBB2 c.2398C>T ;(p.L800F)

Variant ID: 17-37881069-C-T

NM_004448.2(ERBB2):c.2398C>T;(p.L800F)

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:

Mutations in the Kinase Domain of the HER2/ERBB2 Gene Identified in a Wide Variety of Human Cancers.

The Journal Of Molecular Diagnostics : Jmd
Wen, Wenhsiang W; Chen, Wangjuh Sting WS; Xiao, Nick N; Bender, Ryan R; Ghazalpour, Anatole A; Tan, Zheng Z; Swensen, Jeffrey J; Millis, Sherri Z SZ; Basu, Gargi G; Gatalica, Zoran Z; Press, Michael F MF
Publication Date: 2015-09

Variant appearance in text: HER2: L800F
PubMed Link: 26320869
Variant Present in the following documents:
  • Main text
View BVdb publication page