Variant #0000455671 (NC_000006.11:g.109796668A>C, NM_014797.2:c.1222T>G (ZBTB24))
| Chromosome |
6 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.109796668A>C |
| DNA change (hg38) |
g.109475465A>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
ZBTB24_000007 See all 3 reported entries |
| Variant remarks |
Ty1_ZBTB24 variant construct expressed in mESCs could not restore luciferase activity of target promoter, ChIP-qPCR showed impaired binding to target promoter; experiments suggest variant is likely to be pathogenic |
| Reference |
Daxinger, in preparation 2019 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
2.0E-5 View details |
| Owner |
Lucia Daxinger |
| Database submission license |
No license selected |
| Created by |
Lucia Daxinger |
| Date created |
2019-01-29 11:22:51 +01:00 (CET) |
| Date last edited |
2020-06-19 19:45:54 +02:00 (CEST) |

Variant on transcripts
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