Variant #0000632416 (NC_000016.9:g.(?_2098587)_(2124391_2125799)del, NC_000016.9(NM_000548.3):c.(?_-29-1)_(2545+1_2546-1)del (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.(?_2098587)_(2124391_2125799)del |
DNA change (hg38) |
g.(?_2048586)_(2074390_2075798)del |
Published as |
- |
ISCN |
- |
DB-ID |
TSC2_002089 See all 2 reported entries |
Variant remarks |
TSC2 exons 2-22 deleted; found with variant upstream of TSC1 5'UTR c.-1055G>T and TSC2 missense TSC2 c.5359G>A |
Reference |
unpublished |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
De novo |
Segregation |
- |
Frequency |
- |
Re-site |
- |
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 |
2013-02-13 17:56:02 +01:00 (CET) |
Date last edited |
2021-05-04 16:07:11 +02:00 (CEST) |

Variant on transcripts
Screenings
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