Variant #0000002187 (NC_000001.11:g.26177G>A, SLC2A1(NM_006516.2):c.*42900864C>T)

Individual ID 00000458
Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.26177G>A
Published as -
Reference Zhi Xiang Ng et al.(2012)
DB-ID SLC2A1_000001
dbSNP ID rs841846
Frequency -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Nur Aisyah Athirah
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nur Aisyah Athirah
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

Clinical classification     
SLC2A1 NM_006516.2 +/. - c.*42900864C>T - r.(=) p.(=) -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000499 DNA MCA SLC2A1 1 Nur Aisyah Athirah