Variant #0000567657 (NC_000019.9:g.45445602G>T, NM_000483.4:c.-3744G>T (APOC2))

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.45445602G>T
DNA change (hg38) g.44942345G>T
Published as APOC4(NM_001646.2):c.68G>T (p.(Cys23Phe))
ISCN -
DB-ID APOC2_000017
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) 1.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-16 09:30:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
APOC2 NM_000483.4 ?/. - c.-3744G>T r.(?) p.(=)
APOC4 NM_001646.2 ?/. - c.68G>T r.(?) p.(Cys23Phe)
APOC4-APOC2 NR_037932.1 ?/. - n.108G>T r.(?) -


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