Variant #0000187923 (NC_000023.10:g.21886591G>T, NM_015884.3:c.677G>T (MBTPS2))
| Chromosome |
X |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.21886591G>T |
| DNA change (hg38) |
g.21868473G>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
MBTPS2_000020 See all 4 reported entries |
| Variant remarks |
cloned in EYFP fusion construc in pcDNA3.1; CHO expression limited complementation SP2 deficiency |
| Reference |
PubMed: Oeffner 2009 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Emmelien Aten |
| Database submission license |
No license selected |
| Created by |
Emmelien Aten |
| Date created |
2009-08-18 09:19:58 +02:00 (CEST) |
| 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.
|