ERBB2 c.2986C>T ;(p.P996S)

Variant ID: 17-37883083-C-T

NM_004448.2(ERBB2):c.2986C>T;(p.P996S)

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:

Genetic heterogeneity in hepatocellular carcinoma and paired bone metastasis revealed by next-generation sequencing.

International Journal Of Clinical And Experimental Pathology
Jin, Ketao K; Lan, Huanrong H; Wang, Xuanwei X; Lv, Jieqing J
Publication Date: 2017

Variant appearance in text: ERBB2: 2986C>T; Pro996Ser
PubMed Link: 31966388
Variant Present in the following documents:
  • Main text
View BVdb publication page