Variant #0000945136 (NC_000022.10:g.(?_50497820)_(50502628_50506861)del, NM_015166.3:c.(894+1_895-1)_*2192{0} (MLC1))
| Chromosome |
22 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(?_50497820)_(50502628_50506861)del |
| DNA change (hg38) |
g.(?_50059391)_(50064199_50068432)del |
| Published as |
del ex11-12 |
| ISCN |
- |
| DB-ID |
MLC1_000075 See all 3 reported entries |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Rogier Min |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2023-10-31 16:41:00 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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