Variant #0000017957 (NC_000001.10:g.46659545C>T, NM_001243766.1:c.932G>A (POMGNT1))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.46659545C>T |
| DNA change (hg38) |
g.46193873C>T |
| Published as |
1073G>A (R311Q) |
| ISCN |
- |
| DB-ID |
POMGNT1_000008 See all 11 reported entries |
| Variant remarks |
variants c.794G>A (Arg265His) and c.932G>A (Arg311Gln) segregate together |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
2.0E-5 View details |
| Owner |
Anne Polvi |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Anne Polvi |
| Date created |
2013-04-22 14:03:10 +02:00 (CEST) |
| Date last edited |
2022-03-08 20:39:46 +01:00 (CET) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|