Variant #0000976820 (NC_000005.9:g.58750900T>C, NC_000005.9(NM_001165899.1):c.273-239106A>G (PDE4D))

Chromosome 5
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.58750900T>C
DNA change (hg38) -
Published as PDE4D(NM_001104631.2):c.456-239106A>G
ISCN -
DB-ID PDE4D_000094
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDE4D NM_001104631.1 -?/. - c.456-239106A>G r.(=) p.(=)
PDE4D NM_001165899.1 -?/. - c.273-239106A>G r.(=) p.(=)


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