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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