Variant #0000694651 (NC_000016.9:g.2097990_2138713{0}, NM_000548.3:c.-106_*102{0} (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{0}
DNA change (hg38) g.2047989_2088712{0}
Published as -
ISCN -
DB-ID TSC2_001689 See all 3 reported entries
Variant remarks 175790bp multigene deletion; entire TSC2 deleted (ex 1-42) + 9254bp upstream of TSC2 and 125814bp downstream of TSC2; upstream deletion involves NTHL1 gene and downstream deletion involves entire PKD1, RAB26, TRAF7, CASKIN1, MLST8 and BRICD5 genes
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 2020-09-28 10:33:01 +02:00 (CEST)
Date last edited 2021-08-18 14:45:40 +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 +/+ _1_42_ c.-106_*102{0} r.0? p.0? - -


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