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RARA c.659T>C ;(p.L220P)
Variant ID: 17-38508611-T-C
NM_000964.3(
RARA
):c.659T>C;(p.L220P)
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:
Recognition of fold- and function-specific sites in the ligand-binding domain of the thyroid hormone receptor-like family.
Frontiers In Endocrinology
Verma, Sonia S; Chakraborti, Soumyananda S; Singh, Om P OP; Pande, Veena V; Dixit, Rajnikant R; Pandey, Amit V AV; Pandey, Kailash C KC
Publication Date: 2022
Variant appearance in text: RARA: L220P
PubMed Link:
36246927
Variant Present in the following documents:
Main text
fendo-13-981090.pdf
View BVdb publication page
Acute Promyelocytic Leukemia: A Constellation of Molecular Events around a Single PML-RARA Fusion Gene.
Cancers
Liquori, Alessandro A; Ibañez, Mariam M; Sargas, Claudia C; Sanz, Miguel Ángel MÁ; Barragán, Eva E; Cervera, José J
Publication Date: 2020-03-08
Variant appearance in text: RARA: L220P
PubMed Link:
32182684
Variant Present in the following documents:
Main text
cancers-12-00624.pdf
View BVdb publication page