Variant #0000001997 (NC_000003.12:g.114171968C>T, NM_000796.5:c.25G>A (DRD3))

Individual ID 00000412
Chromosome 3
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.114171968C>T
Published as -
Reference Zainal Abidin et al.(2015), ClinVar
DB-ID DRD3_000002
dbSNP ID rs6280
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 2021-02-17 10:42:59 +08:00 (CST)
Date last edited 2021-03-29 09:16:51 +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     
DRD3 NM_000796.5 +/. - c.25G>A - r.(?) p.(Gly9Ser) -
DRD3 NM_001282563.2 +/. - c.25G>A - r.(?) p.(Gly9Ser) -
DRD3 NM_001290809.1 +/. - c.25G>A - r.(?) p.(Gly9Ser) -
DRD3 NM_033663.5 +/. - c.25G>A - r.(?) p.(Gly9Ser) -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000446 DNA MCA DRD3 2 Nur Aisyah Athirah