Variant #0000461220 (NC_000018.9:g.50683873G>A, NM_005215.3:c.1409G>A (DCC))
Chromosome |
18 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.50683873G>A |
DNA change (hg38) |
g.53157503G>A |
Published as |
- |
ISCN |
- |
DB-ID |
DCC_000015 See all 4 reported entries |
Variant remarks |
significantly decreased EGR1-promoter activation, impaired cytoskeletal and membrane rearrangement, CADD = D, GERP = 5.4 |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00284 View details |
Owner |
Ashley Marsh |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2018-04-12 04:39:09 +02:00 (CEST) |
Date last edited |
2020-07-14 19:08:02 +02:00 (CEST) |

Variant on transcripts
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