Variant #0000683593 (NC_000016.9:g.(2103454_2104296)_(2104442_2105402)del, NC_000016.9(NM_000548.3):c.(336+1_337-1)_(481+1_482-1)del (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.(2103454_2104296)_(2104442_2105402)del
DNA change (hg38) -
Published as -
ISCN -
DB-ID TSC2_004315 See all 2 reported entries
Variant remarks exon 5 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 2020-08-24 13:09:23 +02:00 (CEST)
Date last edited 2021-08-18 14:47:59 +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 +?/+? 4i_5i c.(336+1_337-1)_(481+1_482-1)del r.? p.? Hamartin binding domain -


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