BBS7 c.1511G>A ;(p.R504K)

Variant ID: 4-122756299-C-T

NM_176824.2(BBS7):c.1511G>A;(p.R504K)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Epistasis between RET and BBS mutations modulates enteric innervation and causes syndromic Hirschsprung disease.

Proceedings Of The National Academy Of Sciences Of The United States Of America
de Pontual, Loïc L; Zaghloul, Norann A NA; Thomas, Sophie S; Davis, Erica E EE; McGaughey, David M DM; Dollfus, Hélène H; Baumann, Clarisse C; Bessling, Seneca L SL; Babarit, Candice C; Pelet, Anna A; Gascue, Cecilia C; Beales, Philip P; Munnich, Arnold A; Lyonnet, Stanislas S; Etchevers, Heather H; Attie-Bitach, Tania T; Badano, Jose L JL; McCallion, Andrew S AS; Katsanis, Nicholas N; Amiel, Jeanne J
Publication Date: 2009-08-18

Variant appearance in text: BBS7: R504K
PubMed Link: 19666486
Variant Present in the following documents:
  • Main text
View BVdb publication page