Variant #0000305332 (NC_000001.10:g.144930746T>C, NM_022359.5:c.*21451A>G (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.144930746T>C
DNA change (hg38) g.148953729T>G
Published as PDE4DIP(NM_001002811.2):c.963A>G (p.G321=)
ISCN -
DB-ID PDE4DIP_000010
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-03-10 00:20:11 +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.637-6925A>G r.(=) p.(=)
PDE4DIP NM_022359.5 -?/. - c.*21451A>G r.(=) p.(=)


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