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RB1 c.1376C>T ;(p.S459F)
Variant ID: 13-48953773-C-T
NM_000321.2(
RB1
):c.1376C>T;(p.S459F)
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:
Growth factor independence underpins a paroxysmal, aggressive Wnt5aHigh/EphA2Low phenotype in glioblastoma stem cells, conducive to experimental combinatorial therapy.
Journal Of Experimental & Clinical Cancer Research : Cr
Trivieri, Nadia N; Visioli, Alberto A; Mencarelli, Gandino G; Cariglia, Maria Grazia MG; Marongiu, Laura L; Pracella, Riccardo R; Giani, Fabrizio F; Soriano, Amata Amy AA; Barile, Chiara C; Cajola, Laura L; Copetti, Massimiliano M; Palumbo, Orazio O; Legnani, Federico F; DiMeco, Francesco F; Gorgoglione, Leonardo L; Vescovi, Angelo L AL; Binda, Elena E
Publication Date: 2022-04-12
Variant appearance in text: RB1: S459F
PubMed Link:
35414102
Variant Present in the following documents:
13046_2022_2333_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page
Somatic Mutations from Whole Exome Sequencing Analysis of the Patients with Biliary Tract Cancer.
Genomics & Informatics
Yoon, Kyong-Ah KA; Woo, Sang Myung SM; Kim, Yun-Hee YH; Kong, Sun-Young SY; Han, Sung-Sik SS; Park, Sang-Jae SJ; Lee, Woo Jin WJ
Publication Date: 2018-12
Variant appearance in text: RB1: 1376C>T
PubMed Link:
30602096
Variant Present in the following documents:
Main text
gi-2018-16-4-e35.pdf
View BVdb publication page