Variant #0000708685 (NC_000019.9:g.39055858C>T, NM_000540.2:c.12884C>T (RYR1))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.39055858C>T
DNA change (hg38) g.38565218C>T
Published as -
ISCN -
DB-ID RYR1_000304 See all 9 reported entries
Variant remarks ACMG BS1, BP4
Reference Journal: Johnston 2020
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
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 2020-12-08 17:18:38 +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 -?/. - c.12884C>T r.(?) p.(Ala4295Val)


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