Variant #0000807161 (NC_000016.9:g.2141547C>T, NM_000548.3:c.*2936C>T (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.2141547C>T
DNA change (hg38) -
Published as PKD1(NM_001009944.2):c.11589G>A (p.L3863=)
ISCN -
DB-ID PKD1_002887 See all 2 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2022-02-21 16:37:10 +01:00 (CET)
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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.*2936C>T r.(=) p.(=) - -
PKD1 NM_001009944.2 -?/. - c.11589G>A r.(?) p.(Leu3863=) - -
NTHL1 NM_002528.5 -?/. - c.-43699G>A r.(?) p.(=) - -


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