Variant #0000001926 (NC_000005.10:g.174867899T>C, NM_000794.4:c.*863A>G (DRD1))

Individual ID 00000412
Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.174867899T>C
Published as -
Reference Zainal Abidin et al. (2015)
DB-ID DRD1_000002
dbSNP ID rs4867798
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 2021-02-15 15:11:40 +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     
DRD1 NM_000794.4 +/. - c.*863A>G - r.(=) p.(=) -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000428 DNA MCA DRD1 2 Nur Aisyah Athirah