Variant #0000502952 (NC_000001.10:g.144952687G>C, NM_022359.5:c.632C>G (PDE4DIP))

Chromosome 1
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.144952687G>C
DNA change (hg38) g.148931802C>G
Published as PDE4DIP(NM_014644.5):c.221C>G (p.A74G)
ISCN -
DB-ID PDE4DIP_000014
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-23 18:43:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDE4DIP NM_014644.5 -/. - c.221C>G r.(?) p.(Ala74Gly)
PDE4DIP NM_022359.5 -/. - c.632C>G r.(?) p.(Ala211Gly)


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