Variant #0000629918 (NC_000016.9:g.2137969_2138002del, NC_000016.9(NM_000548.3):c.5068+27_5069-47del (TSC2))

Chromosome 16
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.2137969_2138002del
DNA change (hg38) g.2087968_2088001del
Published as -
ISCN -
DB-ID TSC2_000144 See all 30 reported entries
Variant remarks 34bp intronic deletion [caggaaaggtagggccgggtggggccctgcagtg] causes abnormal splicing and the retention of 72bp from intron 39, resulting in the in-frame insertion of 24 new amino acids; variant seen in affected and unaffected individuals
Reference -
ClinVar ID -
dbSNP ID rs137854209
Origin SUMMARY record
Segregation -
Frequency 593/285634 alleles, 1 homozygote
Re-site BsgI-
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 10:22:42 +01:00 (CET)
Date last edited 2021-08-18 14:47:59 +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     
TSC2 NM_000548.3 -/- 39i c.5068+27_5069-47del r.[5068_5069insGTAGGGCCGGGTGGGGCCCTGCAGTGTGGCGCCAAGAGCCCTGGGCCTGGCGTGACCACCAAGTCTCCCCAG];[=] p.Lys1689_Asp1690insGlyArgAlaGlyTrpGlyProAlaValTrpArgGlnGluProTrpAlaTrpArgAspHisGlnValSerPro GAP domain unlikely to affect splicing


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