Variant #0000352567 (NC_000001.10:g.46662407del, NM_001243766.1:c.351del (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.46662407del |
| DNA change (hg38) |
g.46196735del |
| Published as |
350delC |
| ISCN |
- |
| DB-ID |
POMGNT1_000196 See all 3 reported entries |
| Variant remarks |
2 Italian MDDGA3 (MEB) patients (both com-het) and 1 MDDGA3 (MEB) patient (com-het) with unknown ethnicity |
| 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 |
2020-06-04 14:02:30 +02:00 (CEST) |

Variant on transcripts
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