RGD:151728437 Rat Genome Database

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Variant: RGD:151728437 -  Homo sapiens

RGD ID: 151728437
RS ID: rs2101876167
ClinVar ID: CV1388634
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PPOX  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 161,138,780
GRCh38 1 161,168,990
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001350130.2:c.131-3C>A
NM_001350131.2:c.131-3C>A
NM_001365401.1:c.131-3C>A
NM_001350129.2:c.209-3C>A
More... 		09/01/2021 intron variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:PPOX
Accession:XM_047423604
Location:5UTRS;INTRON

Gene Symbol:PPOX
Accession:XM_005245295
Location:INTRON

Gene Symbol:PPOX
Accession:NM_001365398
Location:INTRON

Gene Symbol:PPOX
Accession:XM_011509672
Location:INTRON

Gene Symbol:PPOX
Accession:XM_047423581
Location:INTRON

Gene Symbol:PPOX
Accession:XM_011509671
Location:INTRON

Gene Symbol:PPOX
Accession:XM_011509678
Location:INTRON

Gene Symbol:PPOX
Accession:XM_005245291
Location:INTRON

Gene Symbol:PPOX
Accession:XM_011509668
Location:INTRON

Gene Symbol:PPOX
Accession:NM_001350128
Location:INTRON

Gene Symbol:PPOX
Accession:NM_001365401
Location:INTRON

Gene Symbol:PPOX
Accession:XM_047423592
Location:INTRON

Gene Symbol:PPOX
Accession:NM_000309
Location:INTRON

Gene Symbol:PPOX
Accession:NM_001350130
Location:INTRON

Gene Symbol:PPOX
Accession:NM_001122764
Location:INTRON

Gene Symbol:PPOX
Accession:XM_011509665
Location:INTRON

Gene Symbol:PPOX
Accession:NM_001350131
Location:INTRON

Gene Symbol:PPOX
Accession:XM_017001566
Location:INTRON

Gene Symbol:PPOX
Accession:XM_024447864
Location:INTRON

Gene Symbol:PPOX
Accession:NM_001365400
Location:INTRON

Gene Symbol:PPOX
Accession:XM_011509670
Location:INTRON

Gene Symbol:PPOX
Accession:XM_011509663
Location:INTRON

Gene Symbol:PPOX
Accession:XM_011509673
Location:INTRON

Gene Symbol:PPOX
Accession:XM_011509664
Location:INTRON

Gene Symbol:PPOX
Accession:XM_047423569
Location:INTRON

Gene Symbol:PPOX
Accession:XM_011509667
Location:INTRON

Gene Symbol:PPOX
Accession:XM_006711404
Location:INTRON

Gene Symbol:PPOX
Accession:XM_011509674
Location:INTRON

Gene Symbol:PPOX
Accession:NM_001350129
Location:INTRON

Gene Symbol:PPOX
Accession:NM_001365399
Location:INTRON

Gene Symbol:PPOX
Accession:XR_007061329
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:9536098   PMID:17576681   PMID:19460837   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001966863 CLINVAR
dbSNP (RS) rs2101876167 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PPOX CLINVAR
OMIM 600923 CLINVAR