Variant #0000567662 (NC_000019.9:g.45451745C>T, NM_000483.4:c.10C>T (APOC2))

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.45451745C>T
DNA change (hg38) g.44948488C>T
Published as APOC2(NM_000483.5):c.10C>T (p.R4*)
ISCN -
DB-ID APOC2_000022
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +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     
APOC2 NM_000483.4 +/. - c.10C>T r.(?) p.(Arg4Ter)
APOC4 NM_001646.2 +/. - c.*3183C>T r.(=) p.(=)
APOC4-APOC2 NR_037932.1 +/. - n.1217C>T r.(?) -


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