Variant #0000253665 (NC_000011.9:g.640109A>C, NM_021008.2:c.*4441T>G (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.640109A>C
DNA change (hg38) g.640109A>C
Published as DRD4(NM_000797.3):c.860A>C (p.Q287P), DRD4(NM_000797.3):c.860delinsC (p.(Gln287Pro))
ISCN -
DB-ID DRD4_000029 See all 2 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) 0.00175 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
DRD4 NM_000797.3 -/. - c.860A>C r.(?) p.(Gln287Pro) -
DEAF1 NM_021008.2 -/. - c.*4441T>G r.(=) p.(=) -


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