Variant #0000692689 (NC_000019.9:g.12786964_12786982del, NM_016145.3:c.-6760_-6742del (WDR83OS))

Chromosome 19
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.12786964_12786982del
DNA change (hg38) -
Published as DHPS(NM_001930.4):c.889-21_889-3delCGTGCCCCCGCCTCCCCAC
ISCN -
DB-ID DHPS_000011
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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DHPS NM_001930.3 ?/. - c.889-21_889-3del r.spl? p.?
WDR83OS NM_016145.3 ?/. - c.-6760_-6742del r.(?) p.(=)
WDR83 NM_032332.3 ?/. - c.*478_*496del r.(=) p.(=)


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