Variant #0000252474 (NC_000012.11:g.103248971A>C, PAH(NM_000277.1):c.649T>G)

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.103248971A>C
DNA change (hg38) g.102855193A>C
Published as PAH(NM_000277.1):c.649T>G (p.C217G)
ISCN -
DB-ID PAH_000100
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner VKGL-NL_Utrecht
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PAH NM_000277.1 +/. - c.649T>G r.(?) p.(Cys217Gly)