Variant #0000238253 (NC_000010.10:g.94824276_94824283dup, NM_183374.2:c.844_851dup (CYP26C1))
| Chromosome |
10 |
| 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.94824276_94824283dup |
| DNA change (hg38) |
g.93064519_93064526dup |
| Published as |
- |
| ISCN |
- |
| DB-ID |
CYP26C1_000001 See all 6 reported entries |
| Variant remarks |
expression cloning shows no CYP26C1 activity |
| Reference |
PubMed: Slavotinek 2013 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| 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 |
2017-12-22 11:46:10 +01:00 (CET) |
| Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|