Variant #0000546249 (NC_000012.11:g.103245479C>A, NM_000277.1:c.898G>T (PAH))

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.103245479C>A
DNA change (hg38) g.102851701C>A
Published as PAH(NM_000277.3):c.898G>T (p.(Ala300Ser), p.A300S), PAH(NM_001354304.2):c.898G>T (p.A300S)
ISCN -
DB-ID PAH_000061 See all 74 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00057 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PAH NM_000277.1 +/. - c.898G>T r.(?) p.(Ala300Ser)


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