Variant #0001064336 (NC_000005.9:g.59284361G>C, NM_001165899.1:c.226C>G (PDE4D))

Chromosome 5
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.59284361G>C
DNA change (hg38) -
Published as PDE4D(NM_001165899.2):c.226C>G (p.(Leu76Val))
ISCN -
DB-ID PDE4D_000127
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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDE4D NM_001104631.1 ?/. - c.-94912C>G r.(?) p.(=)
PDE4D NM_001165899.1 ?/. - c.226C>G r.(?) p.(Leu76Val)


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