Variant #0000017076 (NC_000001.10:g.46660515C>T, NC_000001.10(NM_001243766.1):c.652+1G>A (POMGNT1))
| Chromosome |
1 |
| Allele |
Parent #1 |
| 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.46660515C>T |
| DNA change (hg38) |
g.46194843C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
POMGNT1_000044 See all 3 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) |
0 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 |
2025-06-08 15:58:44 +02:00 (CEST) |

Variant on transcripts
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