Variant #0000716660 (NC_000001.10:g.109566131_109566163dup, NC_000001.10(NM_001142551.1):c.-9-20_4dup (WDR47))

Chromosome 1
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.109566131_109566163dup
DNA change (hg38) g.109023509_109023541dup
Published as WDR47(NM_001142550.1):c.4_5ins33 (p.T2delinsIFLFHI*)
ISCN -
DB-ID WDR47_000001
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WDR47 NM_001142551.1 ?/. - c.-9-20_4dup r.spl? p.?


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