Variant #0000455970 (NC_000016.9:g.2134713C>T, NM_000548.3:c.4490C>T (TSC2))
| Chromosome |
16 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2134713C>T |
| DNA change (hg38) |
g.2084712C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TSC2_002451 See all 6 reported entries |
| Variant remarks |
T389/S6K ratio significantly increased compared to wild type TSC2; TSC1 and TSC2 signals not significantly different compared to wild type; variant disrupts TSC2 function; classified as pathogenic |
| Reference |
Nellist, personal communication |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| 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 |
2015-07-22 03:06:15 +02:00 (CEST) |
| Date last edited |
2021-04-23 13:58:39 +02:00 (CEST) |

Variant on transcripts
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