Variant #0000782072 (NC_000016.9:g.(?_2097990)_(2112602_2112972)del, TSC2(NM_000548.3):c.(?_-106)_(1361+1_1362-1)del)
Chromosome |
16 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
Classification method |
- |
Clinical classification |
pathogenic (dominant) |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(?_2097990)_(2112602_2112972)del |
DNA change (hg38) |
g.(?_2047989)_(2062601_2062971)del |
Published as |
- |
ISCN |
- |
DB-ID |
TSC2_003432 See all 2 reported entries |
Variant remarks |
exons 1-13 deleted; 23,515bp deletion extends ~10kb 5' of TSC2 and involves NTHL1 gene, with insertion of 37bp from PKD1 gene |
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 |

Variant on transcripts
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