Variant #0000000413 (NC_000016.9:g.2106196G>A, NC_000016.9(NM_000548.3):c.600-1G>A (TSC2))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.2106196G>A
Reference -
DB-ID TSC2_000009
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2023-10-02 09:26:25 +00:00 (UTC)
Date last edited 2025-08-04 11:58:52 +00:00 (UTC)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Class     
TSC2 NM_000548.3 +/+ - c.600-1G>A r.spl? p.? pathogenic