Variant #0000782523 (NC_000016.9:g.2132513C>G, NC_000016.9(NM_000548.3):c.3883+8C>G (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.2132513C>G
DNA change (hg38) g.2082512C>G
Published as -
ISCN -
DB-ID TSC2_000539 See all 10 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs45517316
Origin SUMMARY record
Segregation -
Frequency 1331/297856 alleles, 23 homozygotes
Re-site HgaI+, BslI-
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0029 View details
Owner Rosemary Ekong
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Rosemary Ekong
Date created 2021-05-04 16:22:13 +02:00 (CEST)
Date last edited 2023-09-28 16:08:21 +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 -/- 32i c.3883+8C>G r.(?) p.(=) - SpliceAI no effect


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