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 |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| 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
|