Variant #0000352560 (NC_000001.10:g.(46660074_46660224)_(46663544_46685376)del, NC_000001.10(NM_001243766.1):c.(-51+1_-50-1)_(751+1_752-1)del (POMGNT1))
| Chromosome |
1 |
| Allele |
Parent #1 |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Probably affects function |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(46660074_46660224)_(46663544_46685376)del |
| DNA change (hg38) |
- |
| Published as |
deletion exons 2–8 |
| ISCN |
- |
| DB-ID |
POMGNT1_000134 See all 2 reported entries |
| Variant remarks |
1 Italian MDDGA3 (MEB) patient (com-het) |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Anne Polvi |
| Date created |
2013-01-31 14:09:45 +01:00 (CET) |
| Date last edited |
2018-01-19 19:56:48 +01:00 (CET) |

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