Variant #0000873108 (NC_000015.9:g.(44884638_44887491)_(44889123_44890374)del)
| Individual ID |
00414064 |
| Chromosome |
15 |
| Allele |
Maternal (inferred) |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic (recessive) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(44884638_44887491)_(44889123_44890374)del |
| DNA change (hg38) |
- |
| Published as |
NM_025137.4 exon 23i_26i |
| ISCN |
- |
| DB-ID |
chr15_005986 |
| Variant remarks |
- |
| Reference |
Pennings et al. 2022, in progress |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Maartje Pennings |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2022-07-27 10:49:59 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
Screenings
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