Variant #0000577959 (NC_000010.10:g.31810587dup, NM_030751.5:c.2324dup (ZEB1))
Individual ID |
00248128 |
Chromosome |
10 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.31810587dup |
DNA change (hg38) |
g.31521659dup |
Published as |
- |
ISCN |
- |
DB-ID |
ZEB1_000044 |
Variant remarks |
- |
Reference |
PubMed: Liskova 2007 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline/De novo (untested) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Cerys Evans |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2015-07-29 18:31:53 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
Screenings
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