Variant #0000782106 (NC_000016.9:g.(2097990_2138713)insN[10000], NM_000548.3:c.(-106_*102)insN[10000] (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_2138713)insN[10000]
DNA change (hg38) g.(2047989_2088712)insN[10000]
Published as -
ISCN -
DB-ID TSC2_001443 See all 2 reported entries
Variant remarks 10kb insertion
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 2021-05-04 16:22:13 +02:00 (CEST)
Date last edited 2024-08-21 19:30:50 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     

Predict-BioInf     
TSC2 NM_000548.3 +/+ _1_42_ c.(-106_*102)insN[10000] r.? p.? - -


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