Variant #0000989467 (NC_000009.11:g.135779530T>C, NC_000009.11(NM_000368.4):c.2041+268A>G (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.135779530T>C
DNA change (hg38) g.132904143T>C
Published as -
ISCN -
DB-ID TSC1_001629 See all 3 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site HgaI+, SfaNI-
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 2024-08-09 23:17:44 +02:00 (CEST)
Date last edited 2024-08-10 00:28:49 +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 -/- 16i c.2041+268A>G r.(=) p.(=) - SpliceAI no effect


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