Variant #0001045078 (NC_000016.9:g.2097990_2118789{0}, NM_000548.3:c.-106_1717-1668{0} (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.2097990_2118789{0}
DNA change (hg38) g.2047989_2068788{0}
Published as -
ISCN -
DB-ID TSC2_004863 See all 2 reported entries
Variant remarks 21902bp deletion; TSC2 exons 1-16 deleted (20800bp) + 1102bp upstream of TSC2; deletion starts upstream within NTHL1 intron 1 and ends in TSC2 intron 16
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
Owner Rosemary Ekong
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Rosemary Ekong
Date created 2025-05-29 00:53:33 +02:00 (CEST)
Date last edited N/A




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     

Predict-BioInf     
TSC2 NM_000548.3 +/+ _1_16i c.-106_1717-1668{0} r.? p.? - -


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