Variant #0000950538 (NC_000016.9:g.2096239G>A, NM_000548.3:c.-1857G>A (TSC2))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.2096239G>A
DNA change (hg38) -
Published as NTHL1(NM_001318193.1):c.268C>T (p.(Gln90Ter)), NTHL1(NM_002528.7):c.244C>T (p.Q82*)
ISCN -
DB-ID NTHL1_000001 See all 23 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) 0.00143 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2023-11-27 17:35:39 +01:00 (CET)
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.-1857G>A r.(?) p.(=) - -
PKD1 NM_001009944.2 +/. - c.*43489C>T r.(=) p.(=) - -
NTHL1 NM_002528.5 +/. - c.268C>T r.(?) p.(Gln90Ter) - -


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