Variant #0000807133 (NC_000016.9:g.2093728C>T, NM_000548.3:c.-4368C>T (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.2093728C>T
DNA change (hg38) -
Published as NTHL1(NM_002528.7):c.526-1G>A
ISCN -
DB-ID NTHL1_000228 See all 5 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) 9.0E-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 2021-09-17 14:40:49 +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.-4368C>T r.(?) p.(=) - -
PKD1 NM_001009944.2 +/. - c.*46000G>A r.(=) p.(=) - -
SLC9A3R2 NM_001130012.2 +/. - c.*5743C>T r.(=) p.(=) - -
NTHL1 NM_002528.5 +/. - c.550-1G>A r.spl? p.? - -


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