Variant #0000001705 (NC_000010.10:g.17147455C>T, NC_000010.10(NM_001081.3):c.1230+1G>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.17147455C>T |
DNA change (hg38) |
g.17105456C>T |
Published as |
- |
ISCN |
- |
DB-ID |
CUBN_000005 |
Variant remarks |
1 Finnish MGA1 family (com-het) |
Reference |
PubMed: Tanner et al. 2004 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
Segregation |
yes |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0 View details |
Owner |
Anne Polvi |
Database submission license |
No license selected |
Created by |
Anne Polvi |
Date created |
2012-09-07 12:38:10 +02:00 (CEST) |
Date last edited |
2020-06-26 13:43:15 +02:00 (CEST) |

Variant on transcripts
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