Variant #0001031174 (NC_000001.10:g.144863438G>T, NM_022359.5:c.*88759C>A (PDE4DIP))

Chromosome 1
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.144863438G>T
DNA change (hg38) -
Published as PDE4DIP(NM_001350520.1):c.6451C>A (p.(Gln2151Lys))
ISCN -
DB-ID PDE4DIP_000036
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) 0.00355 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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDE4DIP NM_014644.5 -?/. - c.5965C>A r.(?) p.(Gln1989Lys)
PDE4DIP NM_022359.5 -?/. - c.*88759C>A r.(=) p.(=)


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