Variant #0000782122 (NC_000016.9:g.[(?_2098587)_(2127728_2129032)del;(2137943_2138048)_(2138713_?)del], NC_000016.9(NM_000548.3):c.(?_-29-1)_(2966+1_2967-1)del(;)(5068+1_5069-1)_(*102_?)del (TSC2))
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.[(?_2098587)_(2127728_2129032)del;(2137943_2138048)_(2138713_?)del] |
DNA change (hg38) |
g.[(?_2048586)_(2077727_2079031)del;(2087942_2088047)_(2088712_?)del] |
Published as |
- |
ISCN |
- |
DB-ID |
TSC2_002430 See all 2 reported entries |
Variant remarks |
exons 2-26 and 40-42 deleted |
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 |
2021-05-04 16:22:13 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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