Variant #0000001999 (NC_000004.12:g.9784221G>T, NM_000798.5:c.568G>T (DRD5))

Individual ID 00000412
Chromosome 4
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.9784221G>T
Published as -
Reference Zainal Abidin et al.(2015)
DB-ID DRD5_000001
dbSNP ID rs144132215
Frequency -
Variant remarks -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
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 10:55:29 +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     
DRD5 NM_000798.5 +/. - c.568G>T - r.(?) p.(Gly190Trp) -



Screenings


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Genes screened     

Variants found     

Owner     
0000000448 DNA MCA DRD5 1 Nur Aisyah Athirah