ERBB2 c.464T>C ;(p.I155T)

Variant ID: 17-37865595-T-C

NM_004448.2(ERBB2):c.464T>C;(p.I155T)

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:

A novel molecular diagnostics platform for somatic and germline precision oncology.

Molecular Genetics & Genomic Medicine
Cabanillas, Rubén R; Diñeiro, Marta M; Castillo, David D; Pruneda, Patricia C PC; Penas, Cristina C; Cifuentes, Guadalupe A GA; de Vicente, Álvaro Á; Durán, Noelia S NS; Álvarez, Rebeca R; Ordóñez, Gonzalo R GR; Cadiñanos, Juan J
Publication Date: 2017-07

Variant appearance in text: ERBB2: 464T>C; I155T
PubMed Link: 28717660
Variant Present in the following documents:
  • Main text
  • MGG3-5-336.pdf
View BVdb publication page