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RARA c.1347C>A ;(p.S449R)
Variant ID: 17-38512436-C-A
NM_000964.3(
RARA
):c.1347C>A;(p.S449R)
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 identified recurrent and novel variants in benzene-induced leukemia.
Bmc Medical Genomics
Lin, Dafeng D; Wang, Dianpeng D; Li, Peimao P; Deng, Lihua L; Zhang, Zhimin Z; Zhang, Yanfang Y; Zhang, Ming M; Zhang, Naixing N
Publication Date: 2023-01-26
Variant appearance in text: RARA: 1347C>A
PubMed Link:
36703207
Variant Present in the following documents:
12920_2023_1442_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page