Variant #0000017038 (NC_000001.10:g.46660031C>T, NM_001243766.1:c.794G>A (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.46660031C>T |
| DNA change (hg38) |
g.46194359C>T |
| Published as |
935G>A (R265H) |
| ISCN |
- |
| DB-ID |
POMGNT1_000019 See all 10 reported entries |
| Variant remarks |
variants c.794G>A (Arg265His) and c.932G>A (Arg311Gln) segregate together, it is unclear which one is (or if both are) causative |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
4.0E-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 |
2022-03-08 20:36:51 +01:00 (CET) |

Variant on transcripts
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