Variant #0000904127 (NC_000012.11:g.103249009T>C, NM_000277.1:c.611A>G (PAH))

Chromosome 12
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.103249009T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID PAH_000241 See all 30 reported entries
Variant remarks cDNA expression cloning shows small reduction instability (0.75 immunoreactivity A293 cells) and 0.80 residual enzymatic activity
Reference PubMed: Knappskog 1996
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 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 2022-11-25 13:43:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PAH NM_000277.1 -/. 6 c.611A>G - p.Tyr204Cys


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