Variant #0000453877 (NC_000019.9:g.39075629T>C, NM_000540.2:c.14693T>C (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.39075629T>C
DNA change (hg38) g.38584989T>C
Published as -
ISCN -
DB-ID RYR1_000166 See all 16 reported entries
Variant remarks in vitro functional study shows altered ryanodine receptor function
Reference European MH Group genetic testing guidelines May 2005; EHMG RYR1 db
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 17:55:40 +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 +/. 102 c.14693T>C r.(?) p.Ile4898Thr


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