Variant #0000598000 (NC_000016.9:g.2130366C>T, NM_000548.3:c.3598C>T (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.2130366C>T |
| DNA change (hg38) |
g.2080365C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TSC2_000056 See all 36 reported entries |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs45438205 |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
1/31378 alleles |
| Re-site |
BpmI+, AvaII- |
| 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 |
2019-10-11 19:09:07 +02:00 (CEST) |
| Date last edited |
2021-12-11 00:56:05 +01:00 (CET) |

Variant on transcripts
|