Variant #0000001735 (NC_000010.10:g.17127755G>C, NM_001081.3:c.1951C>G (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.17127755G>C
DNA change (hg38) g.17085756G>C
Published as -
ISCN -
DB-ID CUBN_000020
Variant remarks 1 Taiwan (Han) MGA1 family (het)
Reference PubMed: Tanner et al. 2012
ClinVar ID -
dbSNP ID rs182512508
Origin SUMMARY record
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00119 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 14:17:55 +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>G r.(1951c>g) p.(Arg651Gly)


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