Variant #0001008629 (NC_000001.10:g.94457539_94476651del, NM_000350.2:c.5585-164_*400{0} (ABCA4))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.94457539_94476651del |
| DNA change (hg38) |
g.93991983_94011095del |
| Published as |
c.5585-164_*1256del |
| ISCN |
- |
| DB-ID |
ABCA4_001552 See all 2 reported entries |
| Variant remarks |
ACMG PVS1, PM2_sup; severity category not assesed |
| Reference |
Journal: Cornelis 2023 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Stéphanie Cornelis |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2024-09-25 16:00:58 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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