Variant #0000906912 (NC_000012.11:g.(?_103232104)_(103311381_?)del, NM_000277.1:c.-473_*849{0} (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.(?_103232104)_(103311381_?)del
DNA change (hg38) g.(?_102838326)_(102917603_?)del
Published as PAHdel, c.-27778delPAH
ISCN -
DB-ID PAH_000401 See all 2 reported entries
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 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)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PAH NM_000277.1 +/. _1_13_ c.-473_*849{0} r.0 p.0


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.