Variant #0000001529 (NC_000004.11:g.178360789del, NM_000027.3:c.336del (AGA))
| Chromosome |
4 |
| Allele |
Both (homozygous) |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.178360789del |
| DNA change (hg38) |
g.177439635del |
| Published as |
- |
| ISCN |
- |
| DB-ID |
AGA_000011 See all 3 reported entries |
| Variant remarks |
1 Dutch AGU patient |
| Reference |
PubMed: Ikonen et al. 1991 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
yes |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Anne Polvi |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Anne Polvi |
| Date created |
2012-08-30 11:33:10 +02:00 (CEST) |
| Date last edited |
2020-06-16 16:39:33 +02:00 (CEST) |

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