Variant #0000597667 (NC_000016.9:g.2126110C>T, NM_000548.3:c.2681C>T (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.2126110C>T |
DNA change (hg38) |
g.2076109C>T |
Published as |
- |
ISCN |
- |
DB-ID |
TSC2_004277 See all 2 reported entries |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs777282955 |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
3/282332 alleles |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
Owner |
Rosemary Ekong |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Rosemary Ekong |
Date created |
2019-10-01 17:44:31 +02:00 (CEST) |
Date last edited |
2021-08-18 14:47:59 +02:00 (CEST) |

Variant on transcripts
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