Variant #0000001744 (NC_000010.10:g.17107550del, NM_001081.3:c.3096del (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.17107550del |
DNA change (hg38) |
g.17065551del |
Published as |
p.Thr1032* |
ISCN |
- |
DB-ID |
CUBN_000029 |
Variant remarks |
1 Northern European MGA1 family (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 |
No license selected |
Created by |
Anne Polvi |
Date created |
2012-09-11 14:32:41 +02:00 (CEST) |
Date last edited |
2020-06-26 13:43:01 +02:00 (CEST) |

Variant on transcripts
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