Variant #0000001141 (NC_000001.10:g.43392789G>A, SLC2A1(NM_006516.2):c.1402C>T)

Individual ID 00001141
Chromosome 1
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.43392789G>A
Reference Klepper J1, Scheffer H, Elsaid MF, Kamsteeg EJ, Leferink M, Ben-Omran T.(2009)
DB-ID SLC2A1_000012
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 ./. 10 c.1402C>T r.(?) p.(Arg468Trp) VariO:0136 DNA substitution; VariO:0313 transition; VariO:0314 pyrimidine transition VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000001141 ? ? SLC2A1 1 Y Yang