Variant #0000001099 (NC_000014.8:g.55310741C>A, GCH1(NM_000161.2):c.747G>T)

Individual ID 00001099
Chromosome 14
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.55310741C>A
Reference Hwu WL1, Wang PJ, Hsiao KJ, Wang TR, Chiou YW, Lee YM.(1999)
DB-ID GCH1_000038
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Y Yang
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Y Yang
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
GCH1 NM_000161.2 ./. 6 c.747G>T r.(?) p.(Arg249Ser) VariO:0136 DNA substitution; VariO:0316 transversion VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000001099 ? ? GCH1 1 Y Yang