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RB1 c.848G>A ;(p.C283Y)
Variant ID: 13-48937080-G-A
NM_000321.2(
RB1
):c.848G>A;(p.C283Y)
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:
Outcome of children with hypodiploid ALL treated with risk-directed therapy based on MRD levels.
Blood
Mullighan, Charles G CG; Jeha, Sima S; Pei, Deqing D; Payne-Turner, Debbie D; Coustan-Smith, Elaine E; Roberts, Kathryn G KG; Waanders, Esmé E; Choi, John K JK; Ma, Xiaotu X; Raimondi, Susana C SC; Fan, Yiping Y; Yang, Wenjian W; Song, Guangchun G; Yang, Jun J JJ; Inaba, Hiroto H; Downing, James R JR; Leung, Wing H WH; Bowman, W Paul WP; Relling, Mary V MV; Evans, William E WE; Zhang, Jinghui J; Campana, Dario D; Pui, Ching-Hon CH
Publication Date: 2015-12-24
Variant appearance in text: RB1: C283Y
PubMed Link:
26527677
Variant Present in the following documents:
Main text
View BVdb publication page