Variant #0000782305 (NC_000016.9:g.2098586_2098741del, NC_000016.9(NM_000548.3):c.-29-2_125del (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.2098586_2098741del
DNA change (hg38) g.2048585_2048740del
Published as -
ISCN -
DB-ID TSC2_001095
Variant remarks part of exon 2 deleted; 156bp genomic deletion starting in intron 1 and involving first 42 codons of exon 2 (including the start codon); splice site affected
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site AciI-, FatI-
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 2021-05-06 00:06:30 +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_2 c.-29-2_125del r.spl p.? Hamartin binding domain -


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