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RYR1 c.464A>C ;(p.Q155P)
Variant ID: 19-38934828-A-C
NM_000540.2(
RYR1
):c.464A>C;(p.Q155P)
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
'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: 464A>C; Q155P
PubMed Link:
30611313
Variant Present in the following documents:
Main text
40478_2018_655_MOESM1_ESM.xlsx, sheet 2
40478_2018_655_MOESM1_ESM.xlsx, sheet 8
40478_2018_655_MOESM1_ESM.xlsx, sheet 7
40478_2018_Article_655.pdf
40478_2018_655_MOESM1_ESM.xlsx, sheet 6
View BVdb publication page