Variant #0000001996 (NC_000003.12:g.114171942T>C, NM_000796.5:c.51A>G (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.114171942T>C
Published as -
Reference Zainal Abidin et al.(2015),ClinVar
DB-ID DRD3_000001
dbSNP ID rs3732783
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 10:39:13 +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.51A>G - r.(=) p.(=) -
DRD3 NM_001282563.2 +/. - c.51A>G - r.(=) p.(=) -
DRD3 NM_001290809.1 +/. - c.51A>G - r.(=) p.(=) -
DRD3 NM_033663.5 +/. - c.51A>G - r.(=) p.(=) -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000446 DNA MCA DRD3 2 Nur Aisyah Athirah