Variant #0000963644 (NC_000005.9:g.58295394_58295395dup, NC_000005.9(NM_001165899.1):c.739-6090_739-6089dup (PDE4D))

Chromosome 5
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.58295394_58295395dup
DNA change (hg38) -
Published as PDE4D(NM_001197223.2):c.-19_-18dupTA
ISCN -
DB-ID PDE4D_000083
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDE4D NM_001104631.1 -/. - c.922-6090_922-6089dup r.(=) p.(=)
PDE4D NM_001165899.1 -/. - c.739-6090_739-6089dup r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.