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
Screenings
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