Variant #0000781909 (NC_000016.9:g.2137942G>T, NM_000548.3:c.5068G>T (TSC2))
| Chromosome |
16 |
| 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.2137942G>T |
| DNA change (hg38) |
g.2087941G>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TSC2_000145 See all 3 reported entries |
| Variant remarks |
predicted missense but last base of exon affected |
| 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 |
2023-10-09 14:07:01 +02:00 (CEST) |

Variant on transcripts
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