Variant #0000453861 (NC_000019.9:g.38939352G>A, NM_000540.2:c.1021G>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.38939352G>A
DNA change (hg38) g.38448712G>A
Published as -
ISCN -
DB-ID RYR1_000087 See all 22 reported entries
Variant remarks in vitro functional study shows altered ryanodine receptor function
Reference European MH Group genetic testing guidelines May 2005
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2009-11-01 22:02:20 +01:00 (CET)
Date last edited 2020-07-15 17:49:45 +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 +/. 11 c.1021G>A r.(?) p.Gly341Arg


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