CCT5 c.97_98delinsCG ;(p.A33R)

Variant ID: 5-10250549-GC-CG

NM_012073.3(CCT5):c.97_98delinsCG;(p.A33R)

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 hypoxia-related signature for clinically predicting diagnosis, prognosis and immune microenvironment of hepatocellular carcinoma patients.

Journal Of Translational Medicine
Zhang, Baohui B; Tang, Bufu B; Gao, Jianyao J; Li, Jiatong J; Kong, Lingming L; Qin, Ling L
Publication Date: 2020-09-04

Variant appearance in text: CCT5: A33R
PubMed Link: 32887635
Variant Present in the following documents:
  • 12967_2020_2492_MOESM1_ESM.xlsx, sheet 1
View BVdb publication page