Variant #0001031195 (NC_000001.10:g.144952220C>T, NM_022359.5:c.910G>A (PDE4DIP))

Chromosome 1
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.144952220C>T
DNA change (hg38) -
Published as PDE4DIP(NM_001002810.4):c.499G>A (p.(Ala167Thr))
ISCN -
DB-ID PDE4DIP_000057
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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDE4DIP NM_014644.5 ?/. - c.499G>A r.(?) p.(Ala167Thr)
PDE4DIP NM_022359.5 ?/. - c.910G>A r.(?) p.(Ala304Thr)


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