Variant #0000683410 (NC_000009.11:g.135819825_135820081del, NC_000009.11(NM_000368.4):c.-295_-144+105del{0} (TSC1))
Chromosome |
9 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Effect unknown |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.135819825_135820081del |
DNA change (hg38) |
g.132944438_132944694del |
Published as |
- |
ISCN |
- |
DB-ID |
TSC1_001437 See all 2 reported entries |
Variant remarks |
exon 1 deleted; the deletion partially removes the promoter region which is reported between nts. -157bp and -744bp; effect on TSC1 expression unknown |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
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 |
2020-08-18 16:52:40 +02:00 (CEST) |
Date last edited |
2022-06-29 22:07:17 +02:00 (CEST) |

Variant on transcripts
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