rs114017096 Rat Genome Database

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Variant: rs114017096 -  Homo sapiens

RGD ID: 15115428
RS ID: rs114017096
ClinVar ID: CV744817
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NPAS3  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 14 34,145,408
GRCh38 14 33,676,202
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NC_000014.9:g.33676202G>A
NC_000014.8:g.34145408G>A
NM_173159.2:c.520-9G>A
NM_001165893.2:c.469-9G>A
More... 		09/24/2018 intron variant benign none provided

Gene Symbol:NPAS3
Accession:XM_005267992
Location:INTRON

Gene Symbol:NPAS3
Accession:NM_022123
Location:INTRON

Gene Symbol:NPAS3
Accession:NM_001394988
Location:INTRON

Gene Symbol:NPAS3
Accession:XM_017021584
Location:INTRON

Gene Symbol:NPAS3
Accession:XM_047431678
Location:INTRON

Gene Symbol:NPAS3
Accession:NM_001164749
Location:INTRON

Gene Symbol:NPAS3
Accession:XM_017021588
Location:INTRON

Gene Symbol:NPAS3
Accession:XM_017021587
Location:INTRON

Gene Symbol:NPAS3
Accession:XM_011537069
Location:INTRON

Gene Symbol:NPAS3
Accession:XM_017021585
Location:INTRON

Gene Symbol:NPAS3
Accession:XM_005267991
Location:INTRON

Gene Symbol:NPAS3
Accession:NM_001165893
Location:INTRON

Gene Symbol:NPAS3
Accession:XM_011537071
Location:INTRON

Gene Symbol:NPAS3
Accession:XM_017021582
Location:INTRON

Gene Symbol:NPAS3
Accession:NM_173159
Location:INTRON

Gene Symbol:NPAS3
Accession:NM_001394989
Location:INTRON

Gene Symbol:NPAS3
Accession:XM_047431680
Location:INTRON

Gene Symbol:NPAS3
Accession:XM_011537067
Location:INTRON

Gene Symbol:NPAS3
Accession:XM_017021583
Location:INTRON

.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV000895023 CLINVAR
dbSNP (RS) rs114017096 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NPAS3 CLINVAR
OMIM 609430 CLINVAR