Variant #0000906636 (NC_000012.11:g.103245479C>A, NM_000277.1:c.898G>T (PAH))
Chromosome |
12 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic (recessive) |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.103245479C>A |
DNA change (hg38) |
g.102851701C>A |
Published as |
- |
ISCN |
- |
DB-ID |
PAH_000061 See all 74 reported entries |
Variant remarks |
allelic phenotype value 9.2, variant associated with mild HPA |
Reference |
PubMed: Hillert 2020, data copied from the BIOPKU database with 3D model |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Unknown |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00057 View details |
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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