Variant #0000000412 (NC_000016.9:g.2138546G>A, NM_000548.3:c.5359G>A (TSC2))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.2138546G>A
Reference -
DB-ID TSC2_000008
Frequency -
Average frequency (gnomAD v.2.1.1) 0.0022 View details
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 09:25:40 +00:00 (UTC)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Class     
TSC2 NM_000548.3 ?/? - c.5359G>A r.(?) p.(Gly1787Ser) -