Variant #0000001142 (NC_000001.10:g.43395365T>C, SLC2A1(NM_006516.2):c.766A>G)

Individual ID 00001142
Chromosome 1
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.43395365T>C
Reference Wang D1, Kranz-Eble P, De Vivo DC.(2000)
DB-ID SLC2A1_000013
Frequency -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
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 ./. 6 c.766A>G r.(?) p.(Lys256Glu) 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     
0000001142 ? ? SLC2A1 1 Y Yang