Variant #0000855572 (NC_000019.9:g.39076780C>T, NM_000540.2:c.14918C>T (RYR1))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.39076780C>T
DNA change (hg38) -
Published as RYR1(NM_000540.3):c.14918C>T (p.P4973L)
ISCN -
DB-ID RYR1_000022 See all 8 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) 3.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-05-09 15:47:41 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RYR1 NM_000540.2 +/. - c.14918C>T r.(?) p.(Pro4973Leu)
MAP4K1 NM_001042600.1 +/. - c.*1608G>A r.(=) p.(=)


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