Variant #0000567673 (NC_000019.9:g.45452270_45452271insCTC, NC_000019.9(NM_000483.4):c.216-146_216-145insCTC (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.45452270_45452271insCTC
DNA change (hg38) g.44949013_44949014insCTC
Published as APOC2(NM_000483.5):c.216-146_216-145insCTC, APOC4-APOC2(NR_037932.1):n.1423-146_1423-145insCTC
ISCN -
DB-ID APOC2_000033
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 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.216-146_216-145insCTC r.(=) p.(=)
APOC4 NM_001646.2 -/. - c.*3708_*3709insCTC r.(=) p.(=)
APOC4-APOC2 NR_037932.1 -/. - n.1423-146_1423-145insCTC r.(?) -


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