Variant #0000613513 (NC_000011.9:g.640078G>A, NM_021008.2:c.*4472C>T (DEAF1))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.640078G>A
DNA change (hg38) g.640078G>A
Published as DRD4(NM_000797.3):c.829G>A (p.D277N, p.(Asp277Asn))
ISCN -
DB-ID DRD4_000037 See all 3 reported entries
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
DRD4 NM_000797.3 -?/. - c.829G>A r.(?) p.(Asp277Asn) -
DEAF1 NM_021008.2 -?/. - c.*4472C>T r.(=) p.(=) -


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