Variant #0000470066 (NC_000009.11:g.135773017_135773018dup, NC_000009.11(NM_000368.4):c.2626-5_2626-4dup (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.135773017_135773018dup
DNA change (hg38) g.132897630_132897631dup
Published as -
ISCN -
DB-ID TSC1_000963 See all 9 reported entries
Variant remarks 2bp duplication of TT
Reference -
ClinVar ID -
dbSNP ID rs5901000
Origin SUMMARY record
Segregation -
Frequency 26685/119574 alleles, 2983 homozygotes
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 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 -/- 20i c.2626-5_2626-4dup r.spl? p.? - -


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