Variant #0000436512 (NC_000015.9:g.65369531G>T, NM_001101362.2:c.378G>T (KBTBD13))
| Chromosome |
15 |
| 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.65369531G>T |
| DNA change (hg38) |
g.65077193G>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
KBTBD13_000007 See all 4 reported entries |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs2946642 |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
0.50 |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.46426 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2010-12-11 18:22:30 +01:00 (CET) |
| Date last edited |
2012-11-02 20:42:42 +01:00 (CET) |

Variant on transcripts
|