Variant #0000469558 (NC_000009.11:g.?, NM_000368.4:c.[-234-u2538_-234-u2503del(+)-234-u2506_-144+4564delins7] (TSC1))
Chromosome |
9 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Probably affects function |
Classification method |
- |
Clinical classification |
likely pathogenic (dominant) |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.? |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
TSC1_000486 See all 2 reported entries |
Variant remarks |
36bp del upstream of ex1; another 7161bp del involves ex1 and flanking sequences, plus insertion of 7 unspecified nts. into this region (origin unknown); 45 nts. between the 2 deletions; promoter region reported as -157bp to -744bp completely deleted |
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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