Variant #0000469873 (NC_000009.11:g.135802607A>C, NM_000368.4:c.191T>G (TSC1))
| Chromosome |
9 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Probably affects function |
| Classification method |
- |
| Clinical classification |
likely pathogenic (dominant) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.135802607A>C |
| DNA change (hg38) |
g.132927220A>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TSC1_000965 See all 6 reported entries |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
BstNI+, PspGI+ |
| 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 |
2019-03-15 13:22:37 +01:00 (CET) |
| Date last edited |
2020-06-19 08:46:34 +02:00 (CEST) |

Variant on transcripts
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