Variant #0000708604 (NC_000019.9:g.38946168C>T, NM_000540.2:c.1654C>T (RYR1))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.38946168C>T
DNA change (hg38) g.38455528C>T
Published as -
ISCN -
DB-ID RYR1_000089 See all 7 reported entries
Variant remarks ACMG PS3_M, PS4_M, PM1, PP1
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.1654C>T r.(?) p.(Arg552Trp)


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