Variant #0000781901 (NC_000016.9:g.2137925_2137942del, NM_000548.3:c.5051_5068del (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.2137925_2137942del
DNA change (hg38) g.2087924_2087941del
Published as -
ISCN -
DB-ID TSC2_003679 See all 6 reported entries
Variant remarks 18bp deletion of CCCTGCAGTGCAGGAAAG includes last base of exon
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
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 2021-09-28 23:54:23 +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 ?/? 39 c.5051_5068del r.(?) p.(Ser1684_Asp1690delinsTyr) GAP domain may affect splicing


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