Variant #0000126937 (NC_000001.10:g.94546067T>A, NM_000350.2:c.1066A>T (ABCA4))
| Chromosome |
1 |
| Allele |
Parent #1 |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
pathogenic (recessive) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.94546067T>A |
| DNA change (hg38) |
g.94080511T>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
ABCA4_000336 See all 2 reported entries |
| Variant remarks |
- |
| Reference |
PubMed: Cornelis 2017, Journal: Cornelis 2017, 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 4.0 International |
| Created by |
Stéphanie Cornelis |
| Date created |
2016-07-29 12:46:24 +02:00 (CEST) |
| Date last edited |
2024-09-25 14:18:42 +02:00 (CEST) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|