Variant #0001059399 (NC_000007.13:g.(?_154537776)_(159125464_?)del)
| Individual ID |
00469594 |
| Chromosome |
7 |
| 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.(?_154537776)_(159125464_?)del |
| DNA change (hg38) |
g.? |
| Published as |
arr[hg19] 7q36.2q36.3(154,537,776-159,125,464)x1 |
| ISCN |
- |
| DB-ID |
chr7_007599 |
| Variant remarks |
- |
| Reference |
PubMed: Retterer 2016 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Unknown |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2025-11-18 12:45:53 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
Screenings
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