Variant #0000174924 (NC_000003.11:g.8787123G>T, NC_000003.11(NM_033337.2):c.115-89G>T (CAV3))
| Chromosome |
3 |
| Allele |
Parent #1 |
| 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.8787123G>T |
| DNA change (hg38) |
g.8745437G>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
CAV3_000034 See all 2 reported entries |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs13060135 |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
0.00-0.18 |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2004-12-17 15:40:34 +01:00 (CET) |
| Date last edited |
2012-11-02 20:40:41 +01:00 (CET) |

Variant on transcripts
|