Variant #0000674787 (NC_000016.9:g.2135032G>A, NC_000016.9(NM_000548.3):c.4569+5G>A (TSC2))
| Chromosome |
16 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Effect unknown |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2135032G>A |
| DNA change (hg38) |
g.2085031G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TSC2_001557 See all 2 reported entries |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs746446349 |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
3/250214 alleles |
| Re-site |
AccI+, BmgBI+ |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
| Owner |
Rosemary Ekong |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Rosemary Ekong |
| Date created |
2020-07-20 14:30:39 +02:00 (CEST) |
| Date last edited |
2021-08-18 14:47:59 +02:00 (CEST) |

Variant on transcripts
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