Variant #0001046541 (NC_000016.9:g.2097826C>T, NM_000548.3:c.-270C>T (TSC2))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.2097826C>T
DNA change (hg38) -
Published as NTHL1(NM_001318193.1):c.23G>A (p.(Gly8Asp))
ISCN -
DB-ID NTHL1_000402
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 2025-07-08 13:22:38 +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     
TSC2 NM_000548.3 ?/. - c.-270C>T r.(?) p.(=) - -
PKD1 NM_001009944.2 ?/. - c.*41902G>A r.(=) p.(=) - -
NTHL1 NM_002528.5 ?/. - c.23G>A r.(?) p.(Gly8Asp) - -


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