Variant #0000457242 (NC_000009.11:g.135820841C>A, NM_000368.4:c.-1055G>T (TSC1))
| Chromosome |
9 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.135820841C>A |
| DNA change (hg38) |
g.132945454C>A |
| Published as |
-234-u841G>T (-1055G>T) [g.2597781G>T, NT_035014.4] |
| ISCN |
- |
| DB-ID |
TSC1_000630 See all 2 reported entries |
| Variant remarks |
reported as poly; nt. numbering for described variant in the context of TSC1 continues from TSC1 5’UTR; found with TSC2 exons 2-22 del and TSC2 missense c.5359G>A; variant upstream of TSC1 5’UTR & in upstream NTHL1 gene (as NM_002528.5:c.139+669C>A) |
| Reference |
unpublished |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Unknown |
| Segregation |
- |
| Frequency |
1/3 individuals tested have the variant |
| Re-site |
NdeI+ |
| 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 |
2013-02-08 20:15:16 +01:00 (CET) |
| Date last edited |
2020-10-30 01:09:10 +01:00 (CET) |

Variant on transcripts
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