Variant #0000453875 (NC_000019.9:g.38991276C>T, NM_000540.2:c.7354C>T (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.38991276C>T
DNA change (hg38) g.38500636C>T
Published as -
ISCN -
DB-ID RYR1_000157 See all 6 reported entries
Variant remarks in vitro functional study shows altered ryanodine receptor function
Reference PubMed: Bannister 2007
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Jorge Oliveira
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2010-05-27 13:20:40 +02:00 (CEST)
Date last edited 2020-07-15 17:52:20 +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 +/. 46 c.7354C>T r.(?) p.Arg2452Trp


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