Variant #0000782305 (NC_000016.9:g.2098586_2098741del, NC_000016.9(NM_000548.3):c.-29-2_125del (TSC2))
Chromosome |
16 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Probably affects function |
Classification method |
- |
Clinical classification |
likely pathogenic (dominant) |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2098586_2098741del |
DNA change (hg38) |
g.2048585_2048740del |
Published as |
- |
ISCN |
- |
DB-ID |
TSC2_001095 |
Variant remarks |
part of exon 2 deleted; 156bp genomic deletion starting in intron 1 and involving first 42 codons of exon 2 (including the start codon); splice site affected |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
- |
Re-site |
AciI-, FatI- |
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 |
2021-05-04 16:22:13 +02:00 (CEST) |
Date last edited |
2021-05-06 00:06:30 +02:00 (CEST) |

Variant on transcripts
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