Variant #0000597990 (NC_000016.9:g.2138453G>A, NM_000548.3:c.5266G>A (TSC2))

Chromosome 16
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.2138453G>A
DNA change (hg38) g.2088452G>A
Published as -
ISCN -
DB-ID TSC2_004243 See all 5 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs375075952
Origin SUMMARY record
Segregation -
Frequency 7/263162 alleles
Re-site HpyCH4V+
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner Rosemary Ekong
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Rosemary Ekong
Date created 2019-10-11 19:09:07 +02:00 (CEST)
Date last edited 2021-08-18 14:46:53 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     

Predict-BioInf     
TSC2 NM_000548.3 -/- 42 c.5266G>A r.(?) p.(Glu1756Lys) GAP domain -


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