BBS7 c.1457A>G ;(p.Y486C)

Variant ID: 4-122756353-T-C

NM_176824.2(BBS7):c.1457A>G;(p.Y486C)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Targeted high-throughput sequencing for diagnosis of genetically heterogeneous diseases: efficient mutation detection in Bardet-Biedl and Alström syndromes.

Journal Of Medical Genetics
Redin, Claire C; Le Gras, Stéphanie S; Mhamdi, Oussema O; Geoffroy, Véronique V; Stoetzel, Corinne C; Vincent, Marie-Claire MC; Chiurazzi, Pietro P; Lacombe, Didier D; Ouertani, Ines I; Petit, Florence F; Till, Marianne M; Verloes, Alain A; Jost, Bernard B; Chaabouni, Habiba Bouhamed HB; Dollfus, Helene H; Mandel, Jean-Louis JL; Muller, Jean J
Publication Date: 2012-08

Variant appearance in text: BBS7: Y486C
PubMed Link: 22773737
Variant Present in the following documents:
  • Main text
  • jmedgenet-2012-100875.pdf
View BVdb publication page