Variant #0000001740 (NC_000010.10:g.17113436_17113437del, NM_001081.3:c.2614_2615del (CUBN))

Chromosome 10
Allele Both (homozygous)
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.17113436_17113437del
DNA change (hg38) g.17071437_17071438del
Published as p.Asp872fs
ISCN -
DB-ID CUBN_000025
Variant remarks 2 Ashkenazi MGA1 patients (hom)
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 14:26:45 +02:00 (CEST)
Date last edited 2020-06-26 13:43:05 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CUBN NM_001081.3 +/+ 19 c.2614_2615del r.(?) p.(Asp872Leufs*3)


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