Variant #0000989373 (NC_000019.9:g.38989863G>A, NM_000540.2:c.7007G>A (RYR1))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.38989863G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID RYR1_000095 See all 9 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs112563513
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-08-04 13:55:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RYR1 NM_000540.2 +/. - c.7007G>A r.(?) p.(Arg2336His)


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