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RARA c.38G>A ;(p.G13D)
Variant ID: 17-38487508-G-A
NM_000964.3(
RARA
):c.38G>A;(p.G13D)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Estrogen receptor α K303R mutation reorganizes its binding to forkhead box protein A1 regions and induces chromatin opening.
Molecular Biology Reports
Nakadai, Tomoyoshi T; Yang, Liying L; Kumegawa, Kohei K; Maruyama, Reo R
Publication Date: 2022-11-27
Variant appearance in text: RARA: G13D
PubMed Link:
36436079
Variant Present in the following documents:
Main text
11033_2022_Article_8089.pdf
View BVdb publication page
Myeloid Sarcoma Type of Acute Promyelocytic Leukemia With a Cryptic Insertion of RARA Into FIP1L1: The Clinical Utility of NGS and Bioinformatic Analyses.
Frontiers In Oncology
Wang, Yongren Y; Rui, Yaoyao Y; Shen, Ying Y; Li, Jian J; Liu, Poning P; Lu, Qin Q; Fang, Yongjun Y
Publication Date: 2021
Variant appearance in text: RARA: 38G>A
PubMed Link:
34249738
Variant Present in the following documents:
Main text
fonc-11-688203.pdf
View BVdb publication page