Variant #0000001726 (NC_000010.10:g.17165587C>T, NM_001081.3:c.489G>A (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.17165587C>T
DNA change (hg38) g.17123588C>T
Published as C.489_490ins137bp; p.Gly164fs
ISCN -
DB-ID CUBN_000011
Variant remarks 1 German 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 13:56:11 +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 +/+ 05 c.489G>A r.489_490ins137 p.Gly164fs


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