Variant #0000453893 (NC_000019.9:g.38931578G>C, NC_000019.9(NM_000540.2):c.165+74G>C (RYR1))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.38931578G>C
DNA change (hg38) g.38440938G>C
Published as g.43623418C>G
ISCN -
DB-ID RYR1_000332
Variant remarks -
Reference PubMed: Robinson 2006
ClinVar ID -
dbSNP ID rs2304145
Origin Germline
Segregation -
Frequency 0.03
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 2019-01-16 18:47:55 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RYR1 NM_000540.2 -/. 2i c.165+74G>C r.(=) p.(=)


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