Variant #0000564941 (NC_000018.9:g.45567075_45567076insG, NM_001039360.2:c.403_404insC (ZBTB7C))
| Chromosome |
18 |
| 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.45567075_45567076insG |
| DNA change (hg38) |
g.48040704_48040705insG |
| Published as |
ZBTB7C(NM_001318841.2):c.403_404insC (p.E135Afs*4) |
| ISCN |
- |
| DB-ID |
ZBTB7C_000001 |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2020-07-14 18:50:03 +02:00 (CEST) |

Variant on transcripts
|