Variant #0000002094 (NC_000004.12:g.9939182G>A, NC_000004.12(NM_001001290.1):c.727+2731C>T (SLC2A9))

Individual ID 00000447
Chromosome 4
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.9939182G>A
Published as -
Reference dbSNP
DB-ID SLC2A9_000002
dbSNP ID rs5028843
Frequency -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nur Aisyah Athirah
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nur Aisyah Athirah
Date created 2021-02-22 11:17:22 +08:00 (CST)
Date last edited 2021-08-01 13:04:07 +08:00 (CST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

Clinical classification     
SLC2A9 NM_001001290.1 +/. - c.727+2731C>T - r.(=) p.(=) -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000485 DNA PCR SLC2A9 3 Nur Aisyah Athirah