Variant #0000001484 (NC_000021.8:g.45196108C>A, NM_000100.3:c.43G>T (CSTB))
| Chromosome |
21 |
| 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.45196108C>A |
| DNA change (hg38) |
g.43776227C>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
CSTB_000014 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs11553836 |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
unknown |
| 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 |
2012-08-27 08:27:14 +02:00 (CEST) |
| Date last edited |
2022-03-10 09:55:26 +01:00 (CET) |

Variant on transcripts
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