Variant #0000632416 (NC_000016.9:g.(?_2098587)_(2124391_2125799)del, NC_000016.9(NM_000548.3):c.(?_-29-1)_(2545+1_2546-1)del (TSC2))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.(?_2098587)_(2124391_2125799)del
DNA change (hg38) g.(?_2048586)_(2074390_2075798)del
Published as -
ISCN -
DB-ID TSC2_002089 See all 2 reported entries
Variant remarks TSC2 exons 2-22 deleted; found with variant upstream of TSC1 5'UTR c.-1055G>T and TSC2 missense TSC2 c.5359G>A
Reference unpublished
ClinVar ID -
dbSNP ID -
Origin De novo
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 2013-02-13 17:56:02 +01:00 (CET)
Date last edited 2021-05-04 16:07:11 +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_22i c.(?_-29-1)_(2545+1_2546-1)del r.? p.? - -



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