Variant #0000889611 (NC_000011.9:g.116706940_116706942del, NM_000040.1:c.*3340_*3342del (APOC3))
| Chromosome |
11 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.116706940_116706942del |
| DNA change (hg38) |
- |
| Published as |
APOA1(NM_000039.1):c.391_393delAAG (p.K131del), APOA1(NM_000039.3):c.391_393delAAG (p.K131del), APOA1(NM_001318021.1):c.64_66delAAG (p.K22del) |
| ISCN |
- |
| DB-ID |
APOA1_000008 See all 3 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_Groningen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Groningen |
| Date created |
2022-11-01 13:01:21 +01:00 (CET) |
| Date last edited |
2024-08-28 13:16:32 +02:00 (CEST) |

Variant on transcripts
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