BBS2 c.339C>A ;(p.Y113*)

Variant ID: 16-56548371-G-T

NM_031885.3(BBS2):c.339C>A;(p.Y113*)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Understanding mutational effects in digenic diseases.

Nucleic Acids Research
Gazzo, Andrea A; Raimondi, Daniele D; Daneels, Dorien D; Moreau, Yves Y; Smits, Guillaume G; Van Dooren, Sonia S; Lenaerts, Tom T
Publication Date: 2017-09-06

Variant appearance in text: BBS: Y113*
PubMed Link: 28911095
Variant Present in the following documents:
  • Main text
  • gkx557.pdf
View BVdb publication page



Genetic interaction of BBS1 mutations with alleles at other BBS loci can result in non-Mendelian Bardet-Biedl syndrome.

American Journal Of Human Genetics
Beales, Philip L PL; Badano, Jose L JL; Ross, Alison J AJ; Ansley, Stephen J SJ; Hoskins, Bethan E BE; Kirsten, Brigitta B; Mein, Charles A CA; Froguel, Philippe P; Scambler, Peter J PJ; Lewis, Richard Alan RA; Lupski, James R JR; Katsanis, Nicholas N
Publication Date: 2003-05

Variant appearance in text: BBS: Y113X
PubMed Link: 12677556
Variant Present in the following documents:
  • Main text
View BVdb publication page