Variant #0000684004 (NC_000016.9:g.(?_2098587)_(2115637_2120456)del, NC_000016.9(NM_000548.3):c.(?_-29-1)_(1716+1_1717-1)del (TSC2))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic (dominant)
DNA change (genomic) (Relative to hg19 / GRCh37) g.(?_2098587)_(2115637_2120456)del
DNA change (hg38) g.(?_2048586)_(2065636_2070455)del
Published as -
ISCN -
DB-ID TSC2_001076 See all 18 reported entries
Variant remarks deletion involves exons 2-16; exon 17 to exon 42 not deleted
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
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 InternationalCreative Commons License
Created by Rosemary Ekong
Date created 2020-08-26 09:13:20 +02:00 (CEST)
Date last edited 2021-08-18 14:45:40 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     

Predict-BioInf     
TSC2 NM_000548.3 +/+ _1i_16i c.(?_-29-1)_(1716+1_1717-1)del r.? p.? - -


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