Variant #0000597990 (NC_000016.9:g.2138453G>A, NM_000548.3:c.5266G>A (TSC2))
Chromosome |
16 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Does not affect function |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2138453G>A |
DNA change (hg38) |
g.2088452G>A |
Published as |
- |
ISCN |
- |
DB-ID |
TSC2_004243 See all 5 reported entries |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs375075952 |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
7/263162 alleles |
Re-site |
HpyCH4V+ |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
3.0E-5 View details |
Owner |
Rosemary Ekong |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Rosemary Ekong |
Date created |
2019-10-11 19:09:07 +02:00 (CEST) |
Date last edited |
2021-08-18 14:46:53 +02:00 (CEST) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|