Variant #0000557330 (NC_000016.9:g.2141777_2141779dup, NM_000548.3:c.*3166_*3168dup (TSC2))

Chromosome 16
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.2141777_2141779dup
DNA change (hg38) g.2091776_2091778dup
Published as PKD1(NM_000296.3):c.11534+3_11534+5dup (p.?), PKD1(NM_001009944.2):c.11537+5_11537+6insGGG
ISCN -
DB-ID PKD1_000081 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +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.*3166_*3168dup r.(=) p.(=) - -
PKD1 NM_001009944.2 -/. - c.11537+3_11537+5dup r.spl? p.? - -
NTHL1 NM_002528.5 -/. - c.-43931_-43929dup r.(?) p.(=) - -


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