Variant #0000508613 (NC_000001.10:g.94471055C>T, NM_000350.2:c.6089G>A (ABCA4))
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.94471055C>T |
DNA change (hg38) |
g.94005499C>T |
Published as |
ABCA4(NM_000350.2):c.6089G>A (p.R2030Q), ABCA4(NM_000350.3):c.6089G>A (p.R2030Q) |
ISCN |
- |
DB-ID |
ABCA4_000029 See all 234 reported entries |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00035 View details |
Owner |
VKGL-NL_Nijmegen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Nijmegen |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2025-02-07 18:57:27 +01:00 (CET) |

Variant on transcripts
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