Variant #0000855613 (NC_000019.9:g.45451796T>G, NC_000019.9(NM_000483.4):c.55+6T>G (APOC2))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.45451796T>G
DNA change (hg38) -
Published as APOC2(NM_000483.5):c.55+6T>G
ISCN -
DB-ID APOC2_000050
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
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     
APOC2 NM_000483.4 +?/. - c.55+6T>G r.(=) p.(=)
APOC4 NM_001646.2 +?/. - c.*3234T>G r.(=) p.(=)
APOC4-APOC2 NR_037932.1 +?/. - n.1262+6T>G r.(?) -


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