TYR c.1025A>G ;(p.N342S)

Variant ID: 11-88924575-A-G

NM_000372.4(TYR):c.1025A>G;(p.N342S)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


The contribution of common regulatory and protein-coding TYR variants to the genetic architecture of albinism.

Nature Communications
Michaud, Vincent V; Lasseaux, Eulalie E; Green, David J DJ; Gerrard, Dave T DT; Plaisant, Claudio C; , ; Fitzgerald, Tomas T; Birney, Ewan E; Arveiler, BenoƮt B; Black, Graeme C GC; Sergouniotis, Panagiotis I PI
Publication Date: 2022-07-08

Variant appearance in text: TYR: 1025A>G
PubMed Link: 35803923
Variant Present in the following documents:
  • 41467_2022_31392_MOESM4_ESM.xlsx, sheet 1
View BVdb publication page



Molecular and clinical characterization of albinism in a large cohort of Italian patients.

Investigative Ophthalmology & Visual Science
Gargiulo, Annagiusi A; Testa, Francesco F; Rossi, Settimio S; Di Iorio, Valentina V; Fecarotta, Simona S; de Berardinis, Teresa T; Iovine, Antonello A; Magli, Adriano A; Signorini, Sabrina S; Fazzi, Elisa E; Galantuomo, Maria Silvana MS; Fossarello, Maurizio M; Montefusco, Sandro S; Ciccodicola, Alfredo A; Neri, Alberto A; Macaluso, Claudio C; Simonelli, Francesca F; Surace, Enrico Maria EM
Publication Date: 2011-03

Variant appearance in text: TYR: 1025A>G
PubMed Link: 20861488
Variant Present in the following documents:
  • Main text
View BVdb publication page