Variant #0000002575 (NC_000023.11:g.74521047dupT, NM_006517.4:c.488dupT (SLC16A2))

Individual ID 00000576
Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.74521047dupT
Published as -
Reference https://journal.unisza.edu.my/ajmb/index.php/ajmb/article/view/178
DB-ID SLC16A2_000001
dbSNP ID -
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 2021-04-08 10:32:27 +08:00 (CST)
Date last edited 2021-08-01 14:07:49 +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     
SLC16A2 NM_006517.4 +/. - c.488dupT - r.(?) p.(Phe164Ilefs*3) -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000634 DNA PCR;SEQ SLC16A2 4 Nur Aisyah Athirah