Variant #0000405608 (NC_000001.10:g.94506761del, NC_000001.10(NM_000350.2):c.3522+5del (ABCA4))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.94506761del |
| DNA change (hg38) |
g.94041205del |
| Published as |
- |
| ISCN |
- |
| DB-ID |
ABCA4_000613 See all 5 reported entries |
| Variant remarks |
expression cloning midigene splicing construct: 0.530 correctly spliced RNA |
| Reference |
PubMed: Sangermano 2018 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Frans Cremers |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2018-06-03 10:15:41 +02:00 (CEST) |
| Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
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