Variant #0000017065 (NC_000001.10:g.46655129C>A, NC_000001.10(NM_001243766.1):c.1869+27G>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.46655129C>A |
| DNA change (hg38) |
g.46189457C>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
POMGNT1_000024 See all 7 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) |
8.0E-5 View details |
| 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 |
2025-03-15 12:20:58 +01:00 (CET) |

Variant on transcripts
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