Variant #0000782072 (NC_000016.9:g.(?_2097990)_(2112602_2112972)del, TSC2(NM_000548.3):c.(?_-106)_(1361+1_1362-1)del)

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)_(2112602_2112972)del
DNA change (hg38) g.(?_2047989)_(2062601_2062971)del
Published as -
ISCN -
DB-ID TSC2_003432 See all 2 reported entries
Variant remarks exons 1-13 deleted; 23,515bp deletion extends ~10kb 5' of TSC2 and involves NTHL1 gene, with insertion of 37bp from PKD1 gene
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
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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 +/+ _1_13i c.(?_-106)_(1361+1_1362-1)del r.? p.? - -