Variant #0000469612 (NC_000009.11:g.135786112T>C, NC_000009.11(NM_000368.4):c.1142-33A>G (TSC1))

Chromosome 9
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.135786112T>C
DNA change (hg38) g.132910725T>C
Published as -
ISCN -
DB-ID TSC1_000076 See all 8 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs6597586
Origin SUMMARY record
Segregation -
Frequency 39432/303658 alleles, 2454 homozygotes
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.12445 View details
Owner Rosemary Ekong
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Rosemary Ekong
Date created 2019-03-15 13:22:37 +01:00 (CET)
Date last edited 2020-11-02 09:57:30 +01:00 (CET)
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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 -/- 11i c.1142-33A>G r.(?) p.(=) - -


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