Variant #0000325438 (NC_000017.10:g.42824485_42824486del, NM_145663.2:c.865_866del (DBF4B))

Chromosome 17
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.42824485_42824486del
DNA change (hg38) g.44747117_44747118del
Published as DBF4B(NM_025104.3):c.865_866del (p.(Ala289CysfsTer74))
ISCN -
DB-ID DBF4B_000005
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 2020-07-13 17:00:22 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DBF4B NM_145663.2 ?/. - c.865_866del r.(?) p.(Ala289CysfsTer74)


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