Variant #0000001702 (NC_000010.10:g.17088532G>C, NC_000010.10(NM_001081.3):c.3330-439C>G (CUBN))
| Chromosome |
10 |
| Allele |
Both (homozygous) |
| 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.17088532G>C |
| DNA change (hg38) |
g.17046533G>C |
| Published as |
IVS23-439C>G (FM2) |
| ISCN |
- |
| DB-ID |
CUBN_000002 |
| Variant remarks |
1 Finnish MGA1 family (hom), 1 Swedish MGA1 family (com-het) |
| Reference |
PubMed: Aminoff et al. 1999, PubMed: Tanner et al. 2004, PubMed: Tanner et al. 2012 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
yes |
| Frequency |
0/151 CON |
| 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 |
2012-09-07 12:18:37 +02:00 (CEST) |
| Date last edited |
2018-03-30 12:16:31 +02:00 (CEST) |

Variant on transcripts
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