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RARA c.219C>T ;(p.P73=)
Variant ID: 17-38504608-C-T
NM_000964.3(
RARA
):c.219C>T;(p.P73=)
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:
First case report of a NUP98-PMX1 rearrangement in de novo acute myeloid leukemia and literature review.
Bmc Medical Genomics
Fu, Weijia W; Huang, Aijie A; Cheng, Hui H; Luo, Yanrong Y; Gao, Lei L; Tang, Gusheng G; Yang, Jianmin J; Wang, Jianmin J; Ni, Xiong X
Publication Date: 2021-05-17
Variant appearance in text: RARA: P73P
PubMed Link:
34001105
Variant Present in the following documents:
12920_2021_979_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page