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RARA c.607T>G ;(p.C203G)
Variant ID: 17-38508299-T-G
NM_000964.3(
RARA
):c.607T>G;(p.C203G)
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:
Vulnerabilities in mIDH2 AML confer sensitivity to APL-like targeted combination therapy.
Cell Research
Mugoni, Vera V; Panella, Riccardo R; Cheloni, Giulia G; Chen, Ming M; Pozdnyakova, Olga O; Stroopinsky, Dina D; Guarnerio, Jlenia J; Monteleone, Emanuele E; Lee, Jonathan David JD; Mendez, Lourdes L; Menon, Archita Venugopal AV; Aster, Jon Christopher JC; Lane, Andrew A AA; Stone, Richard Maury RM; Galinsky, Ilene I; Zamora, José Cervera JC; Lo-Coco, Francesco F; Bhasin, Manoj Kumar MK; Avigan, David D; Longo, Letizia L; Clohessy, John Gerard JG; Pandolfi, Pier Paolo PP
Publication Date: 2019-06
Variant appearance in text: RARA: C203G
PubMed Link:
31024166
Variant Present in the following documents:
Main text
View BVdb publication page