ERBB2 c.2698A>T ;(p.T900S)

Variant ID: 17-37881628-A-T

NM_004448.2(ERBB2):c.2698A>T;(p.T900S)

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:

Deep phylogeny of cancer drivers and compensatory mutations.

Communications Biology
Rochman, Nash D ND; Wolf, Yuri I YI; Koonin, Eugene V EV
Publication Date: 2020-10-02

Variant appearance in text: HER2: T900S
PubMed Link: 33009502
Variant Present in the following documents:
  • Main text
  • 42003_2020_1276_MOESM14_ESM.xlsx, sheet 1
  • 42003_2020_Article_1276.pdf
View BVdb publication page