RYR1 c.13940T>C ;(p.L4647P)

Variant ID: 19-39062852-T-C

NM_000540.2(RYR1):c.13940T>C;(p.L4647P)

This variant was identified in 3 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: RYR1: 13940T>C; Leu4647Pro
PubMed Link: 36823319
Variant Present in the following documents:
  • 41588_2023_1327_MOESM4_ESM.xlsx, sheet 6
View BVdb publication page



Mutations in proteins involved in E-C coupling and SOCE and congenital myopathies.

The Journal Of General Physiology
Rossi, Daniela D; Catallo, Maria Rosaria MR; Pierantozzi, Enrico E; Sorrentino, Vincenzo V
Publication Date: 2022-09-05

Variant appearance in text: RYR1: L4647P
PubMed Link: 35980353
Variant Present in the following documents:
  • Main text
  • JGP_202213115.pdf
View BVdb publication page



Novel excitation-contraction uncoupled RYR1 mutations in patients with central core disease.

Neuromuscular Disorders : Nmd
Kraeva, Natalia N; Zvaritch, Elena E; Rossi, Ann E AE; Goonasekera, Sanjeewa A SA; Zaid, Hilal H; Frodis, Wanda W; Kraev, Alexander A; Dirksen, Robert T RT; Maclennan, David H DH; Riazi, Sheila S
Publication Date: 2013-02

Variant appearance in text: RYR1: 13940T>C
PubMed Link: 23183335
Variant Present in the following documents:
  • Main text
View BVdb publication page