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 International |
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) |

Variant on transcripts
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