Variant #0000017081 (NC_000001.10:g.46659546G>A, NM_001243766.1:c.931C>T (POMGNT1))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely pathogenic (recessive) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.46659546G>A |
| DNA change (hg38) |
g.46193874G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
POMGNT1_000063 See all 5 reported entries |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| 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 |
2013-01-31 14:09:45 +01:00 (CET) |
| Date last edited |
2022-03-08 20:38:52 +01:00 (CET) |

Variant on transcripts
|