Variant #0000866169 (NC_000019.9:g.45451620T>A, NC_000019.9(NM_000483.4):c.-13-103T>A (APOC2))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.45451620T>A
DNA change (hg38) -
Published as APOC2(NM_000483.4):c.-13-103T>A, APOC2(NM_000483.5):c.-13-103T>A, APOC4-APOC2(NR_037932.1):n.1195-103T>A
ISCN -
DB-ID APOC2_000001 See all 2 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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 16:01:56 +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.-13-103T>A r.(=) p.(=)
APOC4 NM_001646.2 -/. - c.*3058T>A r.(=) p.(=)
APOC4-APOC2 NR_037932.1 -/. - n.1195-103T>A r.(?) -


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