Variant #0000187932 (NC_000023.10:g.21861409G>C, NM_015884.3:c.197G>C (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.21861409G>C |
| DNA change (hg38) |
g.21843291G>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
MBTPS2_000004 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs5951639 |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
0.00 |
| 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 |
2017-08-08 20:03:31 +02:00 (CEST) |

Variant on transcripts
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