Variant #0000002139 (NC_000023.10:g.133609245A>G, HPRT1(NM_000194.2):c.169A>G)

Individual ID 00002139
Chromosome X
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.133609245A>G
Reference Gregoric A1, Rabelink GM, Kokalj Vokac N, Varda NM, Zagradisnik B.(2005)
DB-ID HPRT1_000077
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     
HPRT1 NM_000194.2 ./. 3 c.169A>G r.(?) p.(Met57Val) 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     
0000002139 ? ? HPRT1 1 Y Yang