Variant #0000684364 (NC_000009.11:g.135804171T>C, NM_000368.4:c.89A>G (TSC1))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Classification method -
Clinical classification likely benign (dominant)
DNA change (genomic) (Relative to hg19 / GRCh37) g.135804171T>C
DNA change (hg38) g.132928784T>C
Published as -
ISCN -
DB-ID TSC1_000909 See all 5 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs796053452
Origin SUMMARY record
Segregation -
Frequency 3/143324 alleles
Re-site DraI-, MseI-
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 2020-08-26 10:25:17 +02:00 (CEST)
Date last edited 2023-10-09 14:19:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     

Predict-BioInf     
TSC1 NM_000368.4 -?/-? 3 c.89A>G r.(?) p.(Lys30Arg) - -


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