Variant #0001009959 (NC_000001.10:g.94463648G>C, NM_000350.2:c.6498C>G (ABCA4))
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
ACMG |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.94463648G>C |
DNA change (hg38) |
g.93998092G>C |
Published as |
- |
ISCN |
- |
DB-ID |
ABCA4_001373 See all 9 reported entries |
Variant remarks |
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) |
0.00016 View details |
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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