rs754990869 Rat Genome Database

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Variant: rs754990869 -  Homo sapiens

RGD ID: 152068326
RS ID: rs754990869
ClinVar ID: CV1571165
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PDE8B  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 5 76,714,044
GRCh38 5 77,418,219
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001376075.1:c.1249-10C>T
NM_001376073.1:c.1318-10C>T
NM_001376071.1:c.1465-10C>T
NM_001376070.1:c.1468-10C>T
More... 		06/21/2021 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PDE8B
Accession:NM_001376074
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001376073
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001376063
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001349753
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001376066
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_003719
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001376071
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001414623
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001029854
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001349750
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001349749
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001349751
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001376072
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001349748
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001376070
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001376068
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001376065
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001376062
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001376067
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001376075
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001376069
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001029852
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001029853
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001029851
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001349752
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001414622
Location:INTRON

Gene Symbol:PDE8B
Accession:NM_001376064
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002129270 CLINVAR
dbSNP (RS) rs754990869 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PDE8B CLINVAR
OMIM 603390 CLINVAR