RGD:156116289 Rat Genome Database

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Variant: RGD:156116289 -  Homo sapiens

RGD ID: 156116289
ClinVar ID: CV1982520
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PDE8B  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 5 76,703,291
GRCh38 5 77,407,466
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001376066.1:c.1002+9C>T
NM_001349752.3:c.1059+9C>T
NM_001376062.1:c.1062+9C>T
NM_001376072.1:c.1062+9C>T
More... 		05/12/2022 intron variant likely benign none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Gene Symbol:PDE8B
Accession:NM_001029852
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001376072
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001376073
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001376075
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001376063
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001376074
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001029854
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001376069
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001376064
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001349748
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001349751
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001349752
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001414622
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001376067
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001029851
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001376062
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001376071
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001376065
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001029853
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001349749
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001376068
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001414623
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_003719
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001349750
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001349753
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001376070
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001376066
Location:INTRON

.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV002622771 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PDE8B CLINVAR
OMIM 603390 CLINVAR