Variant #0000725541 (NC_000016.9:g.2142488C>G, NM_000548.3:c.*3877C>G (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.2142488C>G
DNA change (hg38) -
Published as PKD1(NM_000296.3):c.11259G>C (p.(Leu3753=)), PKD1(NM_001009944.2):c.11262G>C (p.L3754=)
ISCN -
DB-ID PKD1_001438 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) 0.00494 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 2021-02-08 18:36:18 +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.*3877C>G r.(=) p.(=) - -
PKD1 NM_001009944.2 -/. - c.11262G>C r.(?) p.(Leu3754=) - -
NTHL1 NM_002528.5 -/. - c.-44640G>C r.(?) p.(=) - -


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