Variant #0000001707 (NC_000010.10:g.(?_16865965)_(17171816_?)del, NM_001081.3:c.(?_-52)_(*1009_?)del (CUBN))

Chromosome 10
Allele Maternal (confirmed)
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.(?_16865965)_(17171816_?)del
DNA change (hg38) -
Published as complete CUBN gene deletion
ISCN -
DB-ID CUBN_000007
Variant remarks 1 German (com-het) and 1 Spanish MGA1 family (com-het); Hauck-1 mutation
Reference PubMed: Hauck et al. 2008, PubMed: Tanner et al. 2012
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Anne Polvi
Database submission license No license selected
Created by Anne Polvi
Date created 2012-09-07 12:43:40 +02:00 (CEST)
Date last edited 2017-05-05 19:04:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CUBN NM_001081.3 +/+ 01-25 c.(?_-52)_(*1009_?)del r.0 p.0


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