Variant #0000001095 (NC_000014.8:g.55310851T>C, GCH1(NM_000161.2):c.637A>G)

Individual ID 00001095
Chromosome 14
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.55310851T>C
Reference Steinberger D1, Korinthenberg R, Topka H, Bergh?user M, Wedde R, Müller U.(2000)
DB-ID GCH1_000034
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.637A>G r.(?) p.(Met213Val) VariO:0136 DNA substitution; VariO:0313 transition; VariO:0315 purine transition VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000001095 ? ? GCH1 1 Y Yang