Variant #0000968188 (NC_000016.9:g.2143546C>T, NM_000548.3:c.*4935C>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.2143546C>T
DNA change (hg38) -
Published as LOC105371049(NR_135175.1):n.303+533C>T, PKD1(NM_000296.3):c.11012G>A (p.(Arg3671Gln)), PKD1(NM_001009944.2):c.11015G>A (p.R3672Q)
ISCN -
DB-ID PKD1_000594 See all 5 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) 0.00043 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 2024-02-26 20:06:56 +01:00 (CET)
Date last edited 2024-10-29 21:08:56 +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.*4935C>T r.(=) p.(=) - -
PKD1 NM_001009944.2 -?/. - c.11015G>A r.(?) p.(Arg3672Gln) - -
NTHL1 NM_002528.5 -?/. - c.-45698G>A r.(?) p.(=) - -


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