Variant #0000954076 (NC_000010.10:g.31810297_31810298del, NM_030751.5:c.2034_2035del (ZEB1))
Individual ID |
00444317 |
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.31810297_31810298del |
DNA change (hg38) |
g.31521369_31521370del |
Published as |
2034_2035delAA |
ISCN |
- |
DB-ID |
ZEB1_000067 |
Variant remarks |
- |
Reference |
PubMed: Moon 2021 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2023-12-21 19:04:03 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
Screenings
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