TYR c.649del ;(p.R217Gfs*9)

Variant ID: 11-88911770-GC-G

NM_000372.4(TYR):c.649del;(p.R217Gfs*9)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Retrospective analysis in oculocutaneous albinism patients for the 2.7 kb deletion in the OCA2 gene revealed a co-segregation of the controversial variant, p.R305W.

Cell & Bioscience
Gao, Jackson J; D'Souza, Leera L; Wetherby, Keith K; Antolik, Christian C; Reeves, Melissa M; Adams, David R DR; Tumminia, Santa S; Wang, Xinjing X
Publication Date: 2017

Variant appearance in text: TYR: 649delC
PubMed Link: 28451379
Variant Present in the following documents:
  • Main text
View BVdb publication page



Comprehensive analysis of oculocutaneous albinism among non-Hispanic caucasians shows that OCA1 is the most prevalent OCA type.

The Journal Of Investigative Dermatology
Hutton, Saunie M SM; Spritz, Richard A RA
Publication Date: 2008-10

Variant appearance in text: OCA1: 649delC
PubMed Link: 18463683
Variant Present in the following documents:
  • Main text
View BVdb publication page