Variant #0001009698 (NC_000001.10:g.94480248del, NC_000001.10(NM_000350.2):c.5313-2del (ABCA4))
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
ACMG |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.94480248del |
DNA change (hg38) |
g.94014692del |
Published as |
- |
ISCN |
- |
DB-ID |
ABCA4_001056 See all 12 reported entries |
Variant remarks |
ACMG PVS1, PS4, PP3_m; severity category severe |
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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