Variant #0000907569 (NC_000012.11:g.103310881C>T, NM_000277.1:c.28G>A (PAH))
| Chromosome |
12 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.103310881C>T |
| DNA change (hg38) |
g.102917103C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
PAH_001634 |
| Variant remarks |
- |
| Reference |
PubMed: Hillert 2020, data copied from the BIOPKU database |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Unknown |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2022-12-06 18:01:45 +01:00 (CET) |
| Date last edited |
2024-02-13 15:01:42 +01:00 (CET) |

Variant on transcripts
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