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RARA c.1153C>A ;(p.R385=)
Variant ID: 17-38511655-C-A
NM_000964.3(
RARA
):c.1153C>A;(p.R385=)
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:
WT1 Gene Mutations, rs16754 Variant, and WT1 Overexpression as Prognostic Factors in Acute Myeloid Leukemia Patients.
Journal Of Clinical Medicine
Koczkodaj, Dorota D; Zmorzyński, Szymon S; Grygalewicz, Beata B; Pieńkowska-Grela, Barbara B; Styk, Wojciech W; Popek-Marciniec, Sylwia S; Filip, Agata Anna AA
Publication Date: 2022-03-28
Variant appearance in text: RARA: R385R
PubMed Link:
35407481
Variant Present in the following documents:
Main text
jcm-11-01873.pdf
View BVdb publication page