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.




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