Variant #0000791390 (NC_000016.9:g.2115620T>G, NM_000548.3:c.1700T>G (TSC2))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.2115620T>G
DNA change (hg38) g.2065619T>G
Published as -
ISCN -
DB-ID TSC2_004329 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site BsaHI+, HgaI+
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 2021-07-22 13:30:05 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     

Predict-BioInf     
TSC2 NM_000548.3 ?/? 16 c.1700T>G r.(?) p.(Leu567Arg) Hamartin binding domain unlikely to affect splicing


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