Variant #0000906387 (NC_000012.11:g.103259598_103260548del, NC_000012.11(NM_000277.1):c.442-102_509+781del (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.103259598_103260548del
DNA change (hg38) g.102865820_102866770del
Published as c.442-102_509+781del951, EX5del955, g.50448_51402del955
ISCN -
DB-ID PAH_000353 See all 5 reported entries
Variant remarks allelic phenotype value 0.1, variant associated with classic PKU
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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PAH NM_000277.1 +/. 4i_5i c.442-102_509+781del r.(?) p.(Gly148TrpfsTer29)


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