Variant #0000949586 (NC_000011.9:g.116707838dup, NM_000040.1:c.*4238dup (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.116707838dup |
| DNA change (hg38) |
- |
| Published as |
APOA1(NM_001318017.1):c.85dupC (p.Q29Pfs*30), APOA1(NM_001318017.2):c.85dupC (p.Q29Pfs*30) |
| ISCN |
- |
| DB-ID |
APOA1_000066 See all 2 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_AMC |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_AMC |
| Date created |
2023-11-27 17:35:39 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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