Variant #0000656261 (NC_000009.11:g.135786013G>A, NM_000368.4:c.1208C>T (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.135786013G>A
DNA change (hg38) g.132910626G>A
Published as TSC1(NM_000368.4):c.1208C>T (p.S403L), TSC1(NM_000368.5):c.1208C>T (p.S403L, p.(Ser403Leu))
ISCN -
DB-ID TSC1_000078 See all 11 reported entries
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) 0.00035 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +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 -?/. - c.1208C>T r.(?) p.(Ser403Leu) - -


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