Variant #0000001739 (NC_000010.10:g.17113456C>T, NM_001081.3:c.2594G>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.17113456C>T
DNA change (hg38) g.17071457C>T
Published as -
ISCN -
DB-ID CUBN_000024 See all 2 reported entries
Variant remarks 3 MGA1 families: Albanian, Scottish and Turkish
Reference PubMed: Tanner et al. 2012
ClinVar ID -
dbSNP ID rs138083522
Origin SUMMARY record
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00728 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 14:24:55 +02:00 (CEST)
Date last edited 2017-05-05 18:33:04 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CUBN NM_001081.3 +?/+? 19 c.2594G>A r.(2594g>a) p.(Ser865Asn)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.