Variant #0001040893 (NC_000016.9:g.2093698G>A, NM_000548.3:c.-4398G>A (TSC2))

Chromosome 16
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.2093698G>A
DNA change (hg38) -
Published as NTHL1(NM_002528.7):c.555C>T (p.S185=)
ISCN -
DB-ID NTHL1_000393
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) 1.0E-5 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 2025-05-05 21:14:00 +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.-4398G>A r.(?) p.(=) - -
PKD1 NM_001009944.2 -?/. - c.*46030C>T r.(=) p.(=) - -
SLC9A3R2 NM_001130012.2 -?/. - c.*5713G>A r.(=) p.(=) - -
NTHL1 NM_002528.5 -?/. - c.579C>T r.(?) p.(=) - -


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