Variant #0000629917 (NC_000016.9:g.2137923_2137924insGG, NM_000548.3:c.5049_5050insGG (TSC2))
Chromosome |
16 |
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.2137923_2137924insGG |
DNA change (hg38) |
g.2087922_2087923insGG |
Published as |
- |
ISCN |
- |
DB-ID |
TSC2_001293 See all 2 reported entries |
Variant remarks |
2bp insertion of GG; protein extends beyond stop codon |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
- |
Re-site |
AvaII+, Sau96I+ |
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 |
2020-01-02 10:22:42 +01:00 (CET) |
Date last edited |
2022-01-23 23:19:04 +01:00 (CET) |

Variant on transcripts
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