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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