Variant #0001008796 (NC_000001.10:g.94549781G>A, NC_000001.10(NM_000350.2):c.769-784C>T (ABCA4))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.94549781G>A |
| DNA change (hg38) |
g.94084225G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
ABCA4_001046 See all 61 reported entries |
| Variant remarks |
reduced penetrance reported (21-40%) Runhart 2020 (PMID:32815999); variant likely underreported due to reduced penetrance and intronic location, Runhart 2019 (PMID:31618761); ACMG BP4_m; 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) |
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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