Variant #0000352563 (NC_000001.10:g.46660575del, NM_001243766.1:c.593del (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.46660575del |
| DNA change (hg38) |
g.46194903del |
| Published as |
593delG |
| ISCN |
- |
| DB-ID |
POMGNT1_000051 See all 3 reported entries |
| Variant remarks |
1 American and 1 German MDDGA3 (MEB) patient (both 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
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