Variant #0000001737 (NC_000010.10:g.17113564G>A, NM_001081.3:c.2486C>T (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.17113564G>A
DNA change (hg38) g.17071565G>A
Published as -
ISCN -
DB-ID CUBN_000022
Variant remarks 1 Dutch MGA1 patient (het)
Reference PubMed: Tanner et al. 2012
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
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 14:21:35 +02:00 (CEST)
Date last edited 2017-05-05 18:33:04 +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.2486C>T r.(2486c>u) p.(Ser829Leu)


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