OCA2 c.1901T>A ;(p.I634N)

Variant ID: 15-28196980-A-T

NM_000275.2(OCA2):c.1901T>A;(p.I634N)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


DNA variations in oculocutaneous albinism: an updated mutation list and current outstanding issues in molecular diagnostics.

Human Mutation
Simeonov, Dimitre R DR; Wang, Xinjing X; Wang, Chen C; Sergeev, Yuri Y; Dolinska, Monika M; Bower, Matthew M; Fischer, Roxanne R; Winer, David D; Dubrovsky, Genia G; Balog, Joan Z JZ; Huizing, Marjan M; Hart, Rachel R; Zein, Wadih M WM; Gahl, William A WA; Brooks, Brian P BP; Adams, David R DR
Publication Date: 2013-06

Variant appearance in text: OCA2: 1901T>A
PubMed Link: 23504663
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: OCA2: 1901T>A; I634N
PubMed Link: 18463683
Variant Present in the following documents:
  • Main text
View BVdb publication page