Variant #0000436511 (NC_000015.9:g.65369395C>T, NM_001101362.2:c.242C>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.65369395C>T |
DNA change (hg38) |
g.65077057C>T |
Published as |
- |
ISCN |
- |
DB-ID |
KBTBD13_000006 See all 4 reported entries |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs2919358 |
Origin |
Germline |
Segregation |
- |
Frequency |
0.31-0.50 |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.44925 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
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