Variant #0000453866 (NC_000019.9:g.38990633G>A, NM_000540.2:c.7300G>A (RYR1))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.38990633G>A
DNA change (hg38) g.38499993G>A
Published as -
ISCN -
DB-ID RYR1_000099 See all 28 reported entries
Variant remarks high affinity [3H]ryanodine binding enhanced sensitivity to Ca2+, caffeine and 4-chloro-m-cresol; reduced sensitivity to calmodulin
Reference PubMed: Richter 1997
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2010-03-06 21:30:45 +01:00 (CET)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RYR1 NM_000540.2 +/. 45 c.7300G>A r.7300g>a p.Gly2434Arg


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