Variant #0000002095 (NC_000004.12:g.9961141T>C, NC_000004.12(NM_001001290.1):c.595-19096A>G (SLC2A9))

Individual ID 00000447
Chromosome 4
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.9961141T>C
Published as -
Reference dbSNP
DB-ID SLC2A9_000003
dbSNP ID rs11942223
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 11:18:35 +08:00 (CST)
Date last edited 2021-08-01 13:04:07 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

Clinical classification     
SLC2A9 NM_001001290.1 -/. - c.595-19096A>G - r.(=) p.(=) -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000485 DNA PCR SLC2A9 3 Nur Aisyah Athirah