Variant #0000963643 (NC_000005.9:g.58295390_58295395dup, NC_000005.9(NM_001165899.1):c.739-6094_739-6089dup (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.58295390_58295395dup
DNA change (hg38) -
Published as PDE4D(NM_001197223.2):c.-23_-18dupTATATA
ISCN -
DB-ID PDE4D_000082
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2024-02-26 20:06:56 +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.922-6094_922-6089dup r.(=) p.(=)
PDE4D NM_001165899.1 -?/. - c.739-6094_739-6089dup r.(=) p.(=)


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