Variant #0000554803 (NC_000015.9:g.53905855_53905863del, NC_000015.9(NM_182758.2):c.2780+1_2780+9del (WDR72))

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.53905855_53905863del
DNA change (hg38) g.53613658_53613666del
Published as WDR72(NM_182758.2):c.2872+1_2872+9del (p.?)
ISCN -
DB-ID WDR72_000010
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-06 15:01:05 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WDR72 NM_182758.2 ?/. - c.2780+1_2780+9del r.spl? p.?


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