RYR1 c.8953C>T ;(p.R2985*)

Variant ID: 19-39001158-C-T

NM_000540.2(RYR1):c.8953C>T;(p.R2985*)

This variant was identified in 4 publications

View GRCh38 version.




Publications:


Integrated molecular drivers coordinate biological and clinical states in melanoma.

Nature Genetics
Conway, Jake R JR; Dietlein, Felix F; Taylor-Weiner, Amaro A; AlDubayan, Saud S; Vokes, Natalie N; Keenan, Tanya T; Reardon, Brendan B; He, Meng Xiao MX; Margolis, Claire A CA; Weirather, Jason L JL; Haq, Rizwan R; Schilling, Bastian B; Stephen Hodi, F F; Schadendorf, Dirk D; Liu, David D; Van Allen, Eliezer M EM
Publication Date: 2020-12

Variant appearance in text: RYR1: 8953C>T; R2985*
PubMed Link: 33230298
Variant Present in the following documents:
  • NIHMS1637640-supplement-SuppData1.xlsx, sheet 1
View BVdb publication page



Epigenomic and genomic analysis of transcriptome modulation in skin cutaneous melanoma.

Aging
Chen, Wuzhen W; Cheng, Pu P; Jiang, Jingxin J; Ren, Yunqing Y; Wu, Dang D; Xue, Dan D
Publication Date: 2020-07-07

Variant appearance in text: RYR1: 8953C>T
PubMed Link: 32639949
Variant Present in the following documents:
  • aging-12-103115-s013..xlsx, sheet 1
View BVdb publication page



'Dusty core disease' (DuCD): expanding morphological spectrum of RYR1 recessive myopathies.

Acta Neuropathologica Communications
Garibaldi, Matteo M; Rendu, John J; Brocard, Julie J; Lacene, Emmanuelle E; Fauré, Julien J; Brochier, Guy G; Beuvin, Maud M; Labasse, Clemence C; Madelaine, Angeline A; Malfatti, Edoardo E; Bevilacqua, Jorge Alfredo JA; Lubieniecki, Fabiana F; Monges, Soledad S; Taratuto, Ana Lia AL; Laporte, Jocelyn J; Marty, Isabelle I; Antonini, Giovanni G; Romero, Norma Beatriz NB
Publication Date: 2019-01-05

Variant appearance in text: RYR1: 8953C>T; R2985*
PubMed Link: 30611313
Variant Present in the following documents:
  • Main text
  • 40478_2018_Article_655.pdf
  • 40478_2018_655_MOESM1_ESM.xlsx, sheet 2
  • 40478_2018_655_MOESM1_ESM.xlsx, sheet 7
  • 40478_2018_655_MOESM1_ESM.xlsx, sheet 8
  • 40478_2018_655_MOESM1_ESM.xlsx, sheet 1
  • 40478_2018_655_MOESM1_ESM.xlsx, sheet 3
  • 40478_2018_655_MOESM1_ESM.xlsx, sheet 6
View BVdb publication page



An integrated diagnosis strategy for congenital myopathies.

Plos One
Böhm, Johann J; Vasli, Nasim N; Malfatti, Edoardo E; Le Gras, Stéphanie S; Feger, Claire C; Jost, Bernard B; Monnier, Nicole N; Brocard, Julie J; Karasoy, Hatice H; Gérard, Marion M; Walter, Maggie C MC; Reilich, Peter P; Biancalana, Valérie V; Kretz, Christine C; Messaddeq, Nadia N; Marty, Isabelle I; Lunardi, Joël J; Romero, Norma B NB; Laporte, Jocelyn J
Publication Date: 2013

Variant appearance in text: RYR1: Arg2985*
PubMed Link: 23826317
Variant Present in the following documents:
  • Main text
  • pone.0067527.pdf
View BVdb publication page