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HR c.283_285delinsTGT ;(p.E95C)
Variant ID: 8-21986399-CTC-ACA
NM_005144.4(
HR
):c.283_285delinsTGT;(p.E95C)
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:
Identification of a Costimulatory Molecule-Related Signature for Predicting Prognostic Risk in Prostate Cancer.
Frontiers In Genetics
Ge, Shengdong S; Hua, Xiaoliang X; Chen, Juan J; Xiao, Haibing H; Zhang, Li L; Zhou, Jun J; Liang, Chaozhao C; Tai, Sheng S
Publication Date: 2021
Variant appearance in text: HR: E95C
PubMed Link:
34484286
Variant Present in the following documents:
Main text
View BVdb publication page