Variant #0000620167 (NC_000016.9:g.2110814G>C, NM_000548.3:c.1119G>C (TSC2))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic (dominant)
DNA change (genomic) (Relative to hg19 / GRCh37) g.2110814G>C
DNA change (hg38) g.2060813G>C
Published as -
ISCN -
DB-ID TSC2_002796 See all 5 reported entries
Variant remarks exon 11 skipped - reported in mRNA
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site PmlI+, BpmI-
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 2019-11-15 19:28:56 +01:00 (CET)
Date last edited 2023-08-23 17:29:54 +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 +/+ 11 c.1119G>C r.976_1119del p.Ala326_Gln373del Hamartin binding domain SpliceAI affects splicing


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