Variant #0000469530 (NC_000009.11:g.135773001A[17-21], NM_000368.4:c.2626-4T[17_21] (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.135773001A[17-21] |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TSC1_000175 See all 3 reported entries |
| Variant remarks |
five alleles of 17-21monomer T runs (18 Ts in reference sequence) |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
| 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 09:56:34 +01:00 (CET) |
Variant on transcripts
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