Variant #0000469579 (NC_000009.11:g.?, NM_000368.4:c.[-234-u9132_-144+317del(+)-234-u9141_-234-u9086inv] (TSC1))
| Chromosome |
9 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Probably affects function |
| Classification method |
- |
| Clinical classification |
likely pathogenic (dominant) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.? |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TSC1_000484 See all 2 reported entries |
| Variant remarks |
9540bp deletion; variant includes exon 1, upstream region, and a 56bp inverted sequence upstream of exon 1; promoter region reported between nts. -157bp and -744bp completely deleted |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
| Owner |
Rosemary Ekong |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Rosemary Ekong |
| Date created |
2019-03-15 13:22:37 +01:00 (CET) |
| Date last edited |
2020-11-02 09:56:34 +01:00 (CET) |
Variant on transcripts
|