Variant #0000002546 (NC_000012.12:g.89349306G>A, NM_001946.3:c.1094C>T (DUSP6))

Individual ID 00000557
Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.89349306G>A
Published as -
Reference {DOI: Shifat A.Nowrin et al.(2019):10.4034/PBOCI.2019.191.65}
DB-ID DUSP6_000001
dbSNP ID rs370130918
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 2021-04-04 09:04:46 +08:00 (CST)
Date last edited 2021-08-01 13:36:28 +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     
DUSP6 NM_001946.3 +/. 3 c.1094C>T - r.(?) p.(Thr365Ile) -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000608 DNA PCR;SEQ DUSP6 1 Nur Aisyah Athirah