ERBB2 c.428G>C ;(p.R143P)

Variant ID: 17-37864776-G-C

NM_004448.2(ERBB2):c.428G>C;(p.R143P)

This variant was identified in 2 publications

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

A germline alteration of ERBB2 increases the risk of breast cancer in Chinese Han women with a familial history of malignant tumors.

Oncology Letters
Ju, Yan Y; Wang, Lifeng L; Ta, Shengjun S; Shu, Rui R; Yang, Shanling S; Gao, Xican X; Song, Hongping H; Liu, Liwen L
Publication Date: 2019-09

Variant appearance in text: rs185670819
PubMed Link: 31452768
Variant Present in the following documents:
  • Main text
  • ol-18-03-2885.pdf
View BVdb publication page