Variant #0000557381 (NC_000016.9:g.2154537G>A, NM_000548.3:c.*15926G>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.2154537G>A
DNA change (hg38) g.2104536G>A
Published as PKD1(NM_000296.3):c.8123C>T (p.(Thr2708Met)), PKD1(NM_001009944.2):c.8123C>T (p.T2708M)
ISCN -
DB-ID PKD1_000720 See all 6 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) 0.00961 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
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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.*15926G>A r.(=) p.(=) - -
PKD1 NM_001009944.2 -?/. - c.8123C>T r.(?) p.(Thr2708Met) - -


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