Variant #0000436513 (NC_000015.9:g.65370835C>T, NM_001101362.2:c.*305C>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.65370835C>T |
| DNA change (hg38) |
g.65078497C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
KBTBD13_000008 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs2946643 |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
0.50-1.00 |
| 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 |
2010-12-11 18:22:30 +01:00 (CET) |
| Date last edited |
2012-11-02 20:42:42 +01:00 (CET) |

Variant on transcripts
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