Variant #0000629914 (NC_000016.9:g.2126580_2126581insT, NM_000548.3:c.2831_2832insT (TSC2))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.2126580_2126581insT
DNA change (hg38) g.2076579_2076580insT
Published as -
ISCN -
DB-ID TSC2_001290 See all 2 reported entries
Variant remarks 1bp insertion of T; variant in alternatively spliced exon
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site BpuEI+, DrdI-
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 14:45:40 +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 ?/? 26 c.2831_2832insT r.(?) p.(Lys945Glnfs*15) - -


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