Variant #0000001995 (NC_000011.10:g.113412654G>A, NM_000795.3:c.1040C>T (DRD2))

Individual ID 00000412
Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.113412654G>A
Published as -
Reference Zainal Abidin et al.(2015)
DB-ID DRD2_000003
dbSNP ID rs144999500
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 10:34:51 +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     
DRD2 NM_000795.3 +/. - c.1040C>T - r.(?) p.(Pro347Leu) -
DRD2 NM_016574.3 +/. - c.953C>T - r.(?) p.(Pro318Leu) -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000445 DNA MCA DRD2 2 Nur Aisyah Athirah