Variant #0000469612 (NC_000009.11:g.135786112T>C, NC_000009.11(NM_000368.4):c.1142-33A>G (TSC1))
| Chromosome |
9 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Does not affect function |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.135786112T>C |
| DNA change (hg38) |
g.132910725T>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TSC1_000076 See all 8 reported entries |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs6597586 |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
39432/303658 alleles, 2454 homozygotes |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.12445 View details |
| Owner |
Rosemary Ekong |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Rosemary Ekong |
| Date created |
2019-03-15 13:22:37 +01:00 (CET) |
| Date last edited |
2020-11-02 09:57:30 +01:00 (CET) |

Variant on transcripts
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