Variant #0000725000 (NC_000015.9:g.23892401_23892430del, NM_019066.4:c.474_503del (MAGEL2))
| Chromosome |
15 |
| 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.23892401_23892430del |
| DNA change (hg38) |
- |
| Published as |
MAGEL2(NM_019066.4):c.474_503del (p.(Ala160_Met169del)), MAGEL2(NM_019066.5):c.474_503delAATGGCCCATCCTCCTCCTCCGGGGACCCC (p.A170_M179del) |
| ISCN |
- |
| DB-ID |
MAGEL2_000122 See all 3 reported entries |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00054 View details |
| Owner |
VKGL-NL_Groningen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Groningen |
| Date created |
2021-02-08 18:36:18 +01:00 (CET) |
| Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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