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, p.(Arg2030Gln)) |
| ISCN |
- |
| DB-ID |
ABCA4_000029 See all 235 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 |
2025-11-01 13:22:20 +01:00 (CET) |

Variant on transcripts
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