Variant #0000469991 (NC_000009.11:g.135777121A>G, NC_000009.11(NM_000368.4):c.2392-35T>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.135777121A>G |
| DNA change (hg38) |
g.132901734A>G |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TSC1_000158 See all 18 reported entries |
| Variant remarks |
in-frame deletion of 42bp from exon 19 seen in cDNA |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs11243931 |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
46869/306882 alleles, 3735 homozygotes |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.14146 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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