Variant #0001008599 (NC_000001.10:g.94578548=, NM_000350.2:c.141G>A (ABCA4))
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
ACMG |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.94578548= |
DNA change (hg38) |
g.94112992= |
Published as |
c.141A>G |
ISCN |
- |
DB-ID |
ABCA4_002240 See all 6 reported entries |
Variant remarks |
ACMG BS1, BP4_m, BP7 |
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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