Variant #0000699491 (NC_000009.11:g.135802688C>T, NM_000368.4:c.110G>A (TSC1))
| Chromosome |
9 |
| 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.135802688C>T |
| DNA change (hg38) |
g.132927301C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TSC1_001511 See all 2 reported entries |
| Variant remarks |
reported that variant did not disrupt TSC2 function in vitro |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs750441497 |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
5/250588 alleles |
| Re-site |
FatI+, HpyCH4III- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
2.0E-5 View details |
| Owner |
Mark Nellist |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Rosemary Ekong |
| Date created |
2020-11-02 10:52:17 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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