USH2A c.12859_12863del ;(p.P4287Rfs*4)

Variant ID: 1-215848389-TGGTGG-T

NM_206933.2(USH2A):c.12859_12863del;(p.P4287Rfs*4)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Network expansion of genetic associations defines a pleiotropy map of human cell biology.

Nature Genetics
Barrio-Hernandez, Inigo I; Schwartzentruber, Jeremy J; Shrivastava, Anjali A; Del-Toro, Noemi N; Gonzalez, Asier A; Zhang, Qian Q; Mountjoy, Edward E; Suveges, Daniel D; Ochoa, David D; Ghoussaini, Maya M; Bradley, Glyn G; Hermjakob, Henning H; Orchard, Sandra S; Dunham, Ian I; Anderson, Carl A CA; Porras, Pablo P; Beltrao, Pedro P
Publication Date: 2023-02-23

Variant appearance in text: USH2A: 12859_12863del; Pro4287fs
PubMed Link: 36823319
Variant Present in the following documents:
  • 41588_2023_1327_MOESM4_ESM.xlsx, sheet 6
View BVdb publication page



MYO7A and USH2A gene sequence variants in Italian patients with Usher syndrome.

Molecular Vision
Sodi, Andrea A; Mariottini, Alessandro A; Passerini, Ilaria I; Murro, Vittoria V; Tachyla, Iryna I; Bianchi, Benedetta B; Menchini, Ugo U; Torricelli, Francesca F
Publication Date: 2014

Variant appearance in text: USH2A: 12859_12863del
PubMed Link: 25558175
Variant Present in the following documents:
  • Main text
  • mv-v20-1717.pdf
View BVdb publication page