Variant #0000001725 (NC_000010.10:g.(?_17061982)_(17171816_?)del, NC_000010.10(NM_001081.3):c.(?_-52)_4018+?del (CUBN))

Chromosome 10
Allele Unknown
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.(?_17061982)_(17171816_?)del
DNA change (hg38) -
Published as del Exons 1-28
ISCN -
DB-ID CUBN_000010
Variant remarks 1 Pakistani MGA1 family (com-het)
Reference 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 Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Anne Polvi
Date created 2012-09-11 13:39:06 +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 +/+ 01-28 c.(?_-52)_4018+?del r.? p.?


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.