Variant #0000001132 (NC_000001.10:g.43396720C>T, SLC2A1(NM_006516.2):c.272G>A)

Individual ID 00001132
Chromosome 1
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.43396720C>T
Reference Klepper J1, Willemsen M, Verrips A, Guertsen E, Herrmann R, Kutzick C, Fl?rcken A, Voit T.(2001)
DB-ID SLC2A1_000004
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     
SLC2A1 NM_006516.2 ./. 3 c.272G>A r.(?) p.(Gly91Asp) 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     
0000001132 ? ? SLC2A1 1 Y Yang