Variant #0000525862 (NC_000005.9:g.58334922G>T, NC_000005.9(NM_001165899.1):c.626-124C>A (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.58334922G>T
DNA change (hg38) g.59039095G>T
Published as PDE4D(NM_001197221.1):c.-136C>A (p.(=))
ISCN -
DB-ID PDE4D_000051 See all 2 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) 0.00966 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDE4D NM_001104631.1 -?/. - c.809-124C>A r.(=) p.(=)
PDE4D NM_001165899.1 -?/. - c.626-124C>A r.(=) p.(=)


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