Variant #0000001533 (NC_000004.11:g.178360002A>G, NM_000027.3:c.404T>C (AGA))
| Chromosome |
4 |
| Allele |
Unknown |
| 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.178360002A>G |
| DNA change (hg38) |
g.177438848A>G |
| Published as |
- |
| ISCN |
- |
| DB-ID |
AGA_000015 |
| Variant remarks |
2 Canadian sibs (com-het) with AGU |
| Reference |
PubMed: Laitinen et al. 1997 |
| 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 12:56:09 +02:00 (CEST) |
| Date last edited |
2019-02-27 20:52:21 +01:00 (CET) |

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