Variant #0000782302 (NC_000016.9:g.2098563C>T, NC_000016.9(NM_000548.3):c.-29-25C>T (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.2098563C>T
DNA change (hg38) g.2048562C>T
Published as -
ISCN -
DB-ID TSC2_003023 See all 2 reported entries
Variant remarks variant in intron 1
Reference -
ClinVar ID -
dbSNP ID rs1290479721
Origin SUMMARY record
Segregation -
Frequency 2/281358 alleles
Re-site BsmFI-
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 2021-05-04 16:22:13 +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 ?/? 1i c.-29-25C>T r.(?) p.? - -


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