Variant #0000629926 (NC_000009.11:g.135802671_135802672dup, NM_000368.4:c.127_128dup (TSC1))

Chromosome 9
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic (dominant)
DNA change (genomic) (Relative to hg19 / GRCh37) g.135802671_135802672dup
DNA change (hg38) g.132927284_132927285dup
Published as -
ISCN -
DB-ID TSC1_001370 See all 2 reported entries
Variant remarks 2bp duplication of AA
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site Hpy166II-
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 2020-01-02 10:29:12 +01:00 (CET)
Date last edited 2020-06-19 08:46:34 +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 +/+ 4 c.127_128dup r.(?) p.(Asn43Lysfs*20) - -


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