TYR c.272G>C ;(p.C91S)

Variant ID: 11-88911393-G-C

NM_000372.4(TYR):c.272G>C;(p.C91S)

This variant was identified in 1 publication

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: 272G>C; Cys91Ser
PubMed Link: 35803923
Variant Present in the following documents:
  • 41467_2022_31392_MOESM4_ESM.xlsx, sheet 1
View BVdb publication page