Variant #0000313074 (NC_000015.9:g.85186711del, NM_032856.2:c.1132del (WDR73))

Chromosome 15
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.85186711del
DNA change (hg38) g.84643480del
Published as WDR73(NM_032856.2):c.1132del (p.(Arg378AlafsTer25)), WDR73(NM_032856.3):c.1132delC (p.R378Afs*25), WDR73(NM_032856.5):c.1132delC (p.R378Afs*25)
ISCN -
DB-ID WDR73_000008 See all 3 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WDR73 NM_032856.2 ?/. - c.1132del r.(?) p.(Arg378AlafsTer25)


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