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
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