Variant #0001015215 (NC_000015.9:g.53815547_53815550dup, NC_000015.9(NM_182758.2):c.3149-12_3149-9dup (WDR72))

Chromosome 15
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.53815547_53815550dup
DNA change (hg38) -
Published as WDR72(NM_182758.4):c.3149-14_3149-11dupCTCT
ISCN -
DB-ID WDR72_000023
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-10-29 21:08:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WDR72 NM_182758.2 -/. - c.3149-12_3149-9dup r.(=) p.(=)


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