Variant #0000781386 (NC_000016.9:g.2131676_2131692del, NM_000548.3:c.3691_3707del (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.2131676_2131692del
DNA change (hg38) g.2081675_2081691del
Published as -
ISCN -
DB-ID TSC2_002449 See all 2 reported entries
Variant remarks 17bp deletion of CTGTCTAACGCCCTCAT
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site EcoNI+, AluI-
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 N/A
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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 +/+ 31 c.3691_3707del r.(?) p.(Leu1231Glyfs*3) - -


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