Variant #0000612459 (NC_000010.10:g.31815907G>A, NM_030751.5:c.3090G>A (ZEB1))
Chromosome |
10 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.31815907G>A |
DNA change (hg38) |
g.31526979G>A |
Published as |
ZEB1(NM_001323638.1):c.2436G>A (p.R812=) |
ISCN |
- |
DB-ID |
ZEB1_000056 |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00042 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2019-12-04 15:24:38 +01:00 (CET) |
Date last edited |
2024-02-26 20:06:56 +01:00 (CET) |

Variant on transcripts
|