Variant #0000604204 (NC_000001.10:g.94577135C>T, NM_000350.2:c.161G>A (ABCA4))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.94577135C>T |
| DNA change (hg38) |
g.94111579C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
ABCA4_000240 See all 155 reported entries |
| Variant remarks |
Midigene splicing assay shows 56% expression of deletion and 44% expression of missense variant. |
| Reference |
PubMed: Fadaie et al 2019; Journal: Fadaie et al 2019 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
2.0E-5 View details |
| Owner |
Zeinab Fadaie |
| Database submission license |
Creative Commons Attribution-ShareAlike 4.0 International |
| Created by |
Ivo F.A.C. Fokkema |
| Date created |
2019-11-18 12:54:55 +01:00 (CET) |
| Date last edited |
2020-07-14 21:57:48 +02:00 (CEST) |

Variant on transcripts
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