Variant #0000782080 (NC_000016.9:g.2095496_2102578delinsN[273], NC_000016.9(NM_000548.3):c.-2600_226-765delinsN[273] (TSC2))
| Chromosome |
16 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| Classification method |
- |
| Clinical classification |
pathogenic (dominant) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2095496_2102578delinsN[273] |
| DNA change (hg38) |
g.2045495_2052577delinsN[273] |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TSC2_003588 See all 2 reported entries |
| Variant remarks |
exons 1-3 deleted; 7083bp deletion and 273bp insertion (NG_005895.1:g.1190_8272delins273); starts upstream of untranslated ex 1, includes promoter region (Kobayashi et al, 1997; Mamm Genome. 1997, 8:554-8), ending in intron 3 |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Rosemary Ekong |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Rosemary Ekong |
| Date created |
2021-05-04 16:22:13 +02:00 (CEST) |
| Date last edited |
2021-12-15 22:00:19 +01:00 (CET) |

Variant on transcripts
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