Variant #0000001706 (NC_000010.10:g.17127755G>A, NM_001081.3:c.1951C>T (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.17127755G>A
DNA change (hg38) g.17085756G>A
Published as -
ISCN -
DB-ID CUBN_000006
Variant remarks 1 Turkish MGA1 family (hom)
Reference PubMed: Tanner et al. 2004
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 12:39:51 +02:00 (CEST)
Date last edited 2017-05-05 19:04:32 +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 +/+ 16 c.1951C>T r.(1951C>T) p.(Arg651*)


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