Variant #0000933711 (NC_000001.10:g.94577530C>T, NC_000001.10(NM_000350.2):c.161-395G>A (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.94577530C>T |
| DNA change (hg38) |
g.94111974C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
ABCA4_002453 See all 4 reported entries |
| Variant remarks |
expression cloning midi-gene splicing assay, 0.36 normally spliced mRNA; predicted severity moderate |
| Reference |
PubMed: Corradi 2023, Journal: Corradi 2023 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2023-09-29 13:37:48 +02:00 (CEST) |
| Date last edited |
2023-09-29 16:24:36 +02:00 (CEST) |

Variant on transcripts
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