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TG c.137_138insTG ;(p.D47Efs*60)
Variant ID: 8-133880429-C-CTG
NM_003235.4(
TG
):c.137_138insTG;(p.D47Efs*60)
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Expanding the prostate cancer cell line repertoire with ACRJ-PC28, an AR-negative neuroendocrine cell line derived from an African-Caribbean patient.
Cancer Research Communications
Valentine, Henkel H; Aiken, William W; Morrison, Belinda B; Zhao, Ziran Z; Fowle, Holly H; Wasserman, Jason S JS; Thompson, Elon E; Chin, Warren W; Young, Mark M; Clarke, Shannique S; Gibbs, Denise D; Harrison, Sharon S; McLaughlin, Wayne W; Kwok, Tim T; Jin, Fang F; Campbell, Kerry S KS; Horvath, Anelia A; Thompson, Rory R; Lee, Norman H NH; Zhou, Yan Y; Graña, Xavier X; Ragin, Camille C; Badal, Simone S
Publication Date: 2022-11
Variant appearance in text: TG: 137_138insTG
PubMed Link:
36643868
Variant Present in the following documents:
crc-22-0245-s07.xlsx, sheet 1
View BVdb publication page
Identification of two variants in AGRN and RPL3L genes in a patient with catecholaminergic polymorphic ventricular tachycardia suggesting new candidate disease genes and digenic inheritance.
Clinical Case Reports
Jaouadi, Hager H; Chabrak, Sonia S; Lahbib, Saida S; Abdelhak, Sonia S; Zaffran, Stéphane S
Publication Date: 2022-02
Variant appearance in text: TG: 137_138insTG
PubMed Link:
35341025
Variant Present in the following documents:
CCR3-10-e05339-s001.xlsx, sheet 1
View BVdb publication page
Proteogenomic analysis prioritises functional single nucleotide variants in cancer samples.
Oncotarget
Ma, Shiyong S; Menon, Ranjeeta R; Poulos, Rebecca C RC; Wong, Jason W H JWH
Publication Date: 2017-11-10
Variant appearance in text: TG: 137_138insTG
PubMed Link:
29221171
Variant Present in the following documents:
oncotarget-08-95841-s002.xlsx, sheet 4
View BVdb publication page