Variant #0001026611 (NC_000016.9:g.2142493G>A, NM_000548.3:c.*3882G>A (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.2142493G>A
DNA change (hg38) -
Published as PKD1(NM_001009944.2):c.11257C>T (p.(Arg3753Trp))
ISCN -
DB-ID PKD1_000070 See all 7 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-02-07 18:57:27 +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.*3882G>A r.(=) p.(=) - -
PKD1 NM_001009944.2 +?/. - c.11257C>T r.(?) p.(Arg3753Trp) - -
NTHL1 NM_002528.5 +?/. - c.-44645C>T r.(?) p.(=) - -


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