BBS2 c.334T>C ;(p.F112L)

Variant ID: 16-56548376-A-G

NM_031885.3(BBS2):c.334T>C;(p.F112L)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Novel Candidate Genes and a Wide Spectrum of Structural and Point Mutations Responsible for Inherited Retinal Dystrophies Revealed by Exome Sequencing.

Plos One
de Castro-Miró, Marta M; Tonda, Raul R; Escudero-Ferruz, Paula P; Andrés, Rosa R; Mayor-Lorenzo, Andrés A; Castro, Joaquín J; Ciccioli, Marcela M; Hidalgo, Daniel A DA; Rodríguez-Ezcurra, Juan José JJ; Farrando, Jorge J; Pérez-Santonja, Juan J JJ; Cormand, Bru B; Marfany, Gemma G; Gonzàlez-Duarte, Roser R
Publication Date: 2016

Variant appearance in text: BBS2: 334T>C; F112L
PubMed Link: 28005958
Variant Present in the following documents:
  • Main text
  • pone.0168966.s005.xls, sheet 1
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