RYR1 c.5726_5727del ;(p.E1909Gfs*39)

Variant ID: 19-38979992-AAG-A

NM_000540.2(RYR1):c.5726_5727del;(p.E1909Gfs*39)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Review of RyR1 pathway and associated pathomechanisms.

Acta Neuropathologica Communications
Witherspoon, Jessica W JW; Meilleur, Katherine G KG
Publication Date: 2016-11-17

Variant appearance in text: RYR1: Glu1909GlyfsX39
PubMed Link: 27855725
Variant Present in the following documents:
  • Main text
  • 40478_2016_Article_392.pdf
View BVdb publication page



Genotype-phenotype correlations in recessive RYR1-related myopathies.

Orphanet Journal Of Rare Diseases
Amburgey, Kimberly K; Bailey, Angela A; Hwang, Jean H JH; Tarnopolsky, Mark A MA; Bonnemann, Carsten G CG; Medne, Livija L; Mathews, Katherine D KD; Collins, James J; Daube, Jasper R JR; Wellman, Gregory P GP; Callaghan, Brian B; Clarke, Nigel F NF; Dowling, James J JJ
Publication Date: 2013-08-06

Variant appearance in text: RYR1: 5726_5727delAG; Glu1909GlyfsX39
PubMed Link: 23919265
Variant Present in the following documents:
  • 1750-1172-8-117-S1.xlsx, sheet 2
  • 1750-1172-8-117-S1.xlsx, sheet 1
View BVdb publication page