Variant #0000780223 (NC_000016.9:g.2098629A>G, NM_000548.3:c.13A>G (TSC2))
Chromosome |
16 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Probably does not affect function |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2098629A>G |
DNA change (hg38) |
g.2048628A>G |
Published as |
- |
ISCN |
- |
DB-ID |
TSC2_000932 See all 2 reported entries |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs45517093 |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
1/263920 alleles |
Re-site |
Cac8I+, MwoI+ |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0 View details |
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
|