Variant #0000906925 (NC_000012.11:g.103310863A>G, NM_000277.1:c.46T>C (PAH))

Chromosome 12
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.103310863A>G
DNA change (hg38) g.102917085A>G
Published as -
ISCN -
DB-ID PAH_001626
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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PAH NM_000277.1 ?/. 1 c.46T>C r.(?) p.(Ser16Pro)


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