Variant #0001056649 (NC_000019.9:g.39077958A>G, NC_000019.9(NM_000540.2):c.15022-7A>G (RYR1))

Chromosome 19
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.39077958A>G
DNA change (hg38) -
Published as RYR1(NM_000540.3):c.15022-7A>G
ISCN -
DB-ID MAP4K1_000018
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 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RYR1 NM_000540.2 ?/. - c.15022-7A>G r.(=) p.(=)
MAP4K1 NM_001042600.1 ?/. - c.*430T>C r.(=) p.(=)


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