Variant #0000862619 (NC_000011.9:g.640059_640072del, NM_021008.2:c.*4478_*4491del (DEAF1))

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.640059_640072del
DNA change (hg38) -
Published as DRD4(NM_000797.3):c.810_823delCCGGGGTCCCTGCG (p.R271Pfs*174)
ISCN -
DB-ID DEAF1_000078
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 2022-05-09 15:51:19 +02:00 (CEST)
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.810_823del r.(?) p.(Arg271Profs*174) -
DEAF1 NM_021008.2 +/. - c.*4478_*4491del r.(=) p.(=) -


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