Bibliome.ai browser hg19
Search
About
Stats
FAQ
RARA c.524C>T ;(p.S175F)
Variant ID: 17-38508216-C-T
NM_000964.3(
RARA
):c.524C>T;(p.S175F)
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:
Whole-exome sequencing of primary plasma cell leukemia discloses heterogeneous mutational patterns.
Oncotarget
Cifola, Ingrid I; Lionetti, Marta M; Pinatel, Eva E; Todoerti, Katia K; Mangano, Eleonora E; Pietrelli, Alessandro A; Fabris, Sonia S; Mosca, Laura L; Simeon, Vittorio V; Petrucci, Maria Teresa MT; Morabito, Fortunato F; Offidani, Massimo M; Di Raimondo, Francesco F; Falcone, Antonietta A; Caravita, Tommaso T; Battaglia, Cristina C; De Bellis, Gianluca G; Palumbo, Antonio A; Musto, Pellegrino P; Neri, Antonino A
Publication Date: 2015-07-10
Variant appearance in text: RARA: S175F
PubMed Link:
26046463
Variant Present in the following documents:
oncotarget-06-17543-s002.xls, sheet 1
View BVdb publication page