Variant #0000081435 (NC_000010.10:g.31750008A>G, NM_030751.5:c.101A>G (ZEB1))
| Chromosome |
10 |
| 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.31750008A>G |
| DNA change (hg38) |
g.31461079A>G |
| Published as |
31750009A>G |
| ISCN |
- |
| DB-ID |
ZEB1_000003 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Unknown |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
| Owner |
Hyojin Chae |
| Database submission license |
No license selected |
| Created by |
Hyojin Chae |
| Date created |
2015-10-12 06:16:49 +02:00 (CEST) |
| Date last edited |
2015-10-12 12:14:43 +02:00 (CEST) |

Variant on transcripts
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