Variant #0000632417 (NC_000016.9:g.2138546G>A, NM_000548.3:c.5359G>A (TSC2))

Chromosome 16
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.2138546G>A
DNA change (hg38) g.2088545G>A
Published as -
ISCN -
DB-ID TSC2_000301 See all 12 reported entries
Variant remarks found with variant upstream of TSC1 5'UTR c.-1055G>T and TSC2 exons 2-22 del
Reference unpublished
ClinVar ID -
dbSNP ID rs45517419
Origin Germline
Segregation -
Frequency -
Re-site AluI+, BslI-
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0022 View details
Owner Rosemary Ekong
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Rosemary Ekong
Date created 2015-01-16 19:02:45 +01:00 (CET)
Date last edited 2021-04-23 13:58:39 +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 -/. 42 c.5359G>A r.(?) p.(Gly1787Ser) - -



Screenings

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