Variant #0000321859 (NC_000011.9:g.640061_640108del, NM_021008.2:c.*4446_*4493del (DEAF1))

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.640061_640108del
DNA change (hg38) g.640061_640108del
Published as DRD4(NM_000797.3):c.808_855del (p.(Arg271_Pro286del))
ISCN -
DB-ID DRD4_000022
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.812_859del r.(?) p.(Arg271_Pro286del) -
DEAF1 NM_021008.2 ?/. - c.*4446_*4493del r.(=) p.(=) -


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