Variant #0001022235 (NC_000019.9:g.39013851C>G, NC_000019.9(NM_000540.2):c.10348-6C>G (RYR1))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.39013851C>G
DNA change (hg38) g.38523211C>G
Published as -
ISCN -
DB-ID RYR1_000319 See all 6 reported entries
Variant remarks in vitro analysis 293T cells mini-gene exon trapping assay: effect on RNA inclusion of intron sequences
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner Tjakko van Ham
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2024-11-05 16:15:00 +01:00 (CET)
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 +?/. 68i c.10348-6C>G r.10347_10348ins[10347+1_10348-7;GACCAG] p.Asn3450ValfsTer55


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