Variant #0000981726 (NC_000016.9:g.2143609C>T, NM_000548.3:c.*4998C>T (TSC2))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.2143609C>T
DNA change (hg38) -
Published as PKD1(NM_001009944.2):c.10952G>A (p.G3651D)
ISCN -
DB-ID PKD1_001492 See all 3 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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-04-19 20:27:30 +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.*4998C>T r.(=) p.(=) - -
PKD1 NM_001009944.2 +?/. - c.10952G>A r.(?) p.(Gly3651Asp) - -
NTHL1 NM_002528.5 +?/. - c.-45761G>A r.(?) p.(=) - -


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