Variant #0000597996 (NC_000009.11:g.(?_135766735)_?del(147000), NM_000368.4:c.(?_-234)_?del(147000) (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.(?_135766735)_?del(147000) |
DNA change (hg38) |
g.(?_132891348)_?del(147000) |
Published as |
- |
ISCN |
- |
DB-ID |
TSC1_001345 See all 2 reported entries |
Variant remarks |
147kb deletion involving part of TSC1, GF11B and GTF3C5 (both genes at 5’ of TSC1); deletedTSC1 exons not mentioned and extent of deletion into TSC1 undetermined |
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 |
2019-10-11 19:09:07 +02:00 (CEST) |
Date last edited |
2022-08-17 17:24:06 +02:00 (CEST) |

Variant on transcripts
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