Variant #0000684343 (NC_000009.11:g.135778177A>G, NC_000009.11(NM_000368.4):c.2209-3T>C (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.135778177A>G |
| DNA change (hg38) |
g.132902790A>G |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TSC1_001445 See all 3 reported entries |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs368309229 |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
31/295496 alleles |
| Re-site |
LpnPI+, BfaI- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
7.0E-5 View details |
| Owner |
Rosemary Ekong |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Rosemary Ekong |
| Date created |
2020-08-26 10:25:17 +02:00 (CEST) |
| Date last edited |
2020-11-02 09:57:30 +01:00 (CET) |

Variant on transcripts
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