Variant #0001072956 (NC_000001.10:g.237433827A>G, NM_001035.2:c.79A>G (RYR2))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.237433827A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID RYR2_001595
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1409511801
Origin Unknown
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 2026-04-13 13:35:02 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RYR2 NM_001035.2 ?/. - c.79A>G r.(?) p.(Thr27Ala)


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