Variant #0000187934 (NC_000023.10:g.21861487G>A, NC_000023.10(NM_015884.3):c.224+51G>A (MBTPS2))
| Chromosome |
X |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.21861487G>A |
| DNA change (hg38) |
g.21843369G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
MBTPS2_000006 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs3213452 |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
0.00-0.005 |
| 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 |
2017-08-08 20:03:31 +02:00 (CEST) |
| Date last edited |
2020-07-17 20:12:45 +02:00 (CEST) |

Variant on transcripts
|