Variant #0000598008 (NC_000009.11:g.135802663C>T, NM_000368.4:c.135G>A (TSC1))

Chromosome 9
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.135802663C>T
DNA change (hg38) g.132927276C>T
Published as -
ISCN -
DB-ID TSC1_001326 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs149278759
Origin SUMMARY record
Segregation -
Frequency 4/264282 alleles
Re-site DdeI+, BsaJI-
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 2019-10-11 19:09:07 +02:00 (CEST)
Date last edited 2020-11-02 09:57:30 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     

Predict-BioInf     
TSC1 NM_000368.4 ?/? 4 c.135G>A r.(?) p.(Leu45=) - unlikely to affect splicing


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