Variant #0000506397 (NC_000001.10:g.237774125C>T, NM_001035.2:c.4747C>T (RYR2))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.237774125C>T
DNA change (hg38) g.237610825C>T
Published as RYR2(NM_001035.2):c.4747C>T (p.P1583S), RYR2(NM_001035.3):c.4747C>T (p.P1583S)
ISCN -
DB-ID RYR2_000784 See all 7 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0001 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2019-12-04 14:54:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RYR2 NM_001035.2 ?/. - c.4747C>T r.(?) p.(Pro1583Ser)


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