Variant #0001057703 (NC_000015.9:g.23891901dup, NM_019066.4:c.992dup (MAGEL2))
| Chromosome |
15 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.23891901dup |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
MAGEL2_000289 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Unknown |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
MobiDetails |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
MobiDetails |
| Date created |
2025-11-05 13:51:01 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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