Variant #0000684364 (NC_000009.11:g.135804171T>C, NM_000368.4:c.89A>G (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 (dominant) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.135804171T>C |
| DNA change (hg38) |
g.132928784T>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TSC1_000909 See all 5 reported entries |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs796053452 |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
3/143324 alleles |
| Re-site |
DraI-, MseI- |
| 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 |
2020-08-26 10:25:17 +02:00 (CEST) |
| Date last edited |
2023-10-09 14:19:00 +02:00 (CEST) |

Variant on transcripts
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