Variant #0001009623 (NC_000001.10:g.94486889C>A, NM_000350.2:c.4925G>T (ABCA4))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.94486889C>A |
| DNA change (hg38) |
g.94021333C>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
ABCA4_000895 See all 5 reported entries |
| Variant remarks |
ACMG PM5; severity category benign |
| Reference |
Journal: Cornelis 2023 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.001 View details |
| 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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