ERBB2 c.2668G>T ;(p.A890S)

Variant ID: 17-37881598-G-T

NM_004448.2(ERBB2):c.2668G>T;(p.A890S)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Germline variation in cancer-susceptibility genes in a healthy, ancestrally diverse cohort: implications for individual genome sequencing.

Plos One
Bodian, Dale L DL; McCutcheon, Justine N JN; Kothiyal, Prachi P; Huddleston, Kathi C KC; Iyer, Ramaswamy K RK; Vockley, Joseph G JG; Niederhuber, John E JE
Publication Date: 2014

Variant appearance in text: ERBB2: A890S
PubMed Link: 24728327
Variant Present in the following documents:
  • pone.0094554.s002.xlsx, sheet 3
View BVdb publication page



Direct resequencing of the complete ERBB2 coding sequence reveals an absence of activating mutations in ERBB2 amplified breast cancer.

Genes, Chromosomes & Cancer
Zito, Christina I CI; Riches, David D; Kolmakova, Julia J; Simons, Jan J; Egholm, Michael M; Stern, David F DF
Publication Date: 2008-07

Variant appearance in text: ERBB2: A890S
PubMed Link: 18418848
Variant Present in the following documents:
  • Main text
View BVdb publication page