Variant #0000597667 (NC_000016.9:g.2126110C>T, NM_000548.3:c.2681C>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.2126110C>T
DNA change (hg38) g.2076109C>T
Published as -
ISCN -
DB-ID TSC2_004277 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs777282955
Origin SUMMARY record
Segregation -
Frequency 3/282332 alleles
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-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 2019-10-01 17:44:31 +02:00 (CEST)
Date last edited 2021-08-18 14:47:59 +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 ?/? 24 c.2681C>T r.(?) p.(Ala894Val) - unlikely to affect splicing


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