Variant #0000864411 (NC_000016.9:g.2141559C>A, NM_000548.3:c.*2948C>A (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.2141559C>A
DNA change (hg38) -
Published as PKD1(NM_000296.3):c.11574G>T (p.(Pro3858=)), PKD1(NM_001009944.2):c.11577G>T (p.P3859=)
ISCN -
DB-ID NTHL1_000296 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) 0.00188 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited 2023-07-07 10:10:56 +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.*2948C>A r.(=) p.(=) - -
PKD1 NM_001009944.2 -/. - c.11577G>T r.(?) p.(Pro3859=) - -
NTHL1 NM_002528.5 -/. - c.-43711G>T r.(?) p.(=) - -


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