Variant #0000001705 (NC_000010.10:g.17147455C>T, NC_000010.10(NM_001081.3):c.1230+1G>A (CUBN))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.17147455C>T
DNA change (hg38) g.17105456C>T
Published as -
ISCN -
DB-ID CUBN_000005
Variant remarks 1 Finnish MGA1 family (com-het)
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) 0 View details
Owner Anne Polvi
Database submission license No license selected
Created by Anne Polvi
Date created 2012-09-07 12:38:10 +02:00 (CEST)
Date last edited 2020-06-26 13:43:15 +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 +?/+? 11i c.1230+1G>A r.spl? p.?


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