Variant #0000544832 (NC_000011.9:g.640253C>G, NM_021008.2:c.*4297G>C (DEAF1))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.640253C>G
DNA change (hg38) g.640253C>G
Published as DRD4(NM_000797.3):c.1004C>G (p.A335G)
ISCN -
DB-ID DEAF1_000034
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0026 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
DRD4 NM_000797.3 -/. - c.1004C>G r.(?) p.(Ala335Gly) -
DEAF1 NM_021008.2 -/. - c.*4297G>C r.(=) p.(=) -


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