Variant #0000997593 (NC_000009.11:g.135819922A>C, NC_000009.11(NM_000368.4):c.-144+8T>G (TSC1))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.135819922A>C
DNA change (hg38) -
Published as TSC1(NM_000368.4):c.-144+8T>G (p.?)
ISCN -
DB-ID TSC1_001636
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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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 -?/. - c.-144+8T>G r.(=) p.(=) - -
GFI1B NM_004188.4 -?/. - c.-34327A>C r.(?) p.(=) - -


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