Variant #0000802149 (NC_000005.9:g.59064226A>G, NC_000005.9(NM_001165899.1):c.272+220089T>C (PDE4D))

Chromosome 5
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.59064226A>G
DNA change (hg38) -
Published as PDE4D(NM_001197218.1):c.110T>C (p.(Leu37Pro))
ISCN -
DB-ID PDE4D_000069
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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDE4D NM_001104631.1 -?/. - c.455+124769T>C r.(=) p.(=)
PDE4D NM_001165899.1 -?/. - c.272+220089T>C r.(=) p.(=)


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