Variant #0000408138 (NC_000010.10:g.121429394G>A, NM_004281.3:c.212G>A (BAG3))
| 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.121429394G>A |
| DNA change (hg38) |
g.119669882G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
BAG3_000003 See all 7 reported entries |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs35434411 |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.02006 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2010-03-11 21:40:57 +01:00 (CET) |
| Date last edited |
2012-11-02 20:40:23 +01:00 (CET) |

Variant on transcripts
|