Variant #0000906852 (NC_000012.11:g.103234285G>A, NM_000277.1:c.1208C>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.103234285G>A
DNA change (hg38) g.102840507G>A
Published as -
ISCN -
DB-ID PAH_000027 See all 83 reported entries
Variant remarks allelic phenotype value 9.3, 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) 0.0006 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PAH NM_000277.1 +/. 12 c.1208C>T r.(?) p.(Ala403Val)


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