Variant #0000453891 (NC_000019.9:g.38924814T>C, NC_000019.9(NM_000540.2):c.45+300T>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.38924814T>C
DNA change (hg38) g.38434174T>C
Published as g.43616654C>T
ISCN -
DB-ID RYR1_000330
Variant remarks -
Reference PubMed: Robinson 2006
ClinVar ID -
dbSNP ID rs919781
Origin Germline
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 2009-11-01 22:02:20 +01:00 (CET)
Date last edited 2019-01-16 18:47:55 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RYR1 NM_000540.2 -/. 1i c.45+300T>C r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.