Variant #0000953787 (NC_000016.9:g.2120572G>A, NM_000548.3:c.1832G>A (TSC2))
Chromosome |
16 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2120572G>A |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
TSC2_000105 See all 101 reported entries |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs28934872 |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
MobiDetails |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
MobiDetails |
Date created |
2023-12-19 15:03:01 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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