Variant #0000979463 (NC_000011.9:g.14665765C>T, NM_000922.3:c.144C>T (PDE3B))

Chromosome 11
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.14665765C>T
DNA change (hg38) -
Published as PDE3B(NM_000922.4):c.144C>T (p.(Phe48=))
ISCN -
DB-ID PDE3B_000006
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) 0.00018 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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDE3B NM_000922.3 ?/. - c.144C>T r.(?) p.(=)
PSMA1 NM_002786.3 ?/. - c.-123920G>A r.(?) p.(=)


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