Variant #0000933342 (NC_000010.10:g.18429682del, NM_201596.2:c.17del (CACNB2))
Chromosome |
10 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.18429682del |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
CACNB2_000153 |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs786205787 |
Origin |
Unknown |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0 View details |
Owner |
MobiDetails |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
MobiDetails |
Date created |
2023-09-14 14:03:01 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
|