Variant #0000782226 (NC_000016.9:g.2115652G>A, NC_000016.9(NM_000548.3):c.1716+16G>A (TSC2))
| Chromosome |
16 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Probably does not affect function |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2115652G>A |
| DNA change (hg38) |
g.2065651G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TSC2_000716 See all 2 reported entries |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs45517189 |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
12/288344 alleles |
| Re-site |
BssSI- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
3.0E-5 View details |
| 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 |
N/A |

Variant on transcripts
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