Variant #0000892654 (NC_000016.9:g.2141796G>A, NM_000548.3:c.*3185G>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.2141796G>A
DNA change (hg38) -
Published as PKD1(NM_000296.3):c.11520C>T (p.(Asn3840=)), PKD1(NM_001009944.2):c.11523C>T (p.N3841=)
ISCN -
DB-ID PKD1_001387 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) 0.00163 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 2022-11-01 13:41:49 +01:00 (CET)
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.*3185G>A r.(=) p.(=) - -
PKD1 NM_001009944.2 -/. - c.11523C>T r.(?) p.(Asn3841=) - -
NTHL1 NM_002528.5 -/. - c.-43948C>T r.(?) p.(=) - -


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