Variant #0000439315 (NC_000002.11:g.220284876C>T, NM_001927.3:c.638C>T (DES))
Chromosome |
2 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.220284876C>T |
DNA change (hg38) |
g.219420154C>T |
Published as |
- |
ISCN |
- |
DB-ID |
DES_000020 See all 20 reported entries |
Variant remarks |
cloned in pcDNA3, expressed in SW13 and C2C12 cells; DES normal |
Reference |
PubMed: Goudeau 2006 |
ClinVar ID |
- |
dbSNP ID |
rs41272699 |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00932 View details |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2008-06-20 20:39:37 +02:00 (CEST) |
Date last edited |
2020-07-14 21:54:44 +02:00 (CEST) |

Variant on transcripts
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