Variant #0000699529 (NC_000009.11:g.135820786_135820787delinsTT, NM_000368.4:c.-1001_-1000delinsAA (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.135820786_135820787delinsTT |
| DNA change (hg38) |
g.132945399_132945400delinsTT |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TSC1_000535 See all 2 reported entries |
| Variant remarks |
2bp deletion of GC and 2bp insertion of AA; common variant in 5' upstream region; HGVS nomenclature = NG_012386.1:g.4234_4235delinsAA |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs386739091 |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| 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 |
2020-11-02 10:52:17 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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