RGD:155987616 Rat Genome Database

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Variant: RGD:155987616 -  Homo sapiens

RGD ID: 155987616
ClinVar ID: CV1884142
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FPR1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 19 52,249,840
GRCh38 19 51,746,587
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NC_000019.9:g.52249840G>A
NM_002029.3:c.408C>T
LRG_146p1:p.His136=
NP_002020.1:p.His136=
More... 		12/19/2021 synonymous variant likely benign Gingival disease
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
CV1884142Humangingival disease  IAGP 8554872ClinVar Annotator: match by term: Gingival diseaseClinVarPMID:28492532
Gene Symbol:FPR1
Accession:NM_001193306
Location:EXON
Amino Acid Prediction: H to H (synonymous)
Amino Acid Position: 136
Amino Acid Sequence
(Calculated using NCBI transcript definition)
METNSSLPTNISGGTPAVSAGYLFLDIITYLVFAVTFVLGVLGNGLVIWVAGFRMTHTVTTISYLNLAVADFCFTSTLPF
FMVRKAMGGHWPFGWFLCKFVFTIVDINLFGSVFLIALIALDRCVCVLHPVWTQNHRTVSLAKKVIIGPWVMALLLTLPV
IIRVTTVPGKTGTVACTFNFSPWTNDPKERINVAVAMLTVRGIIRFIIGFSAPMSIVAVSYGLIATKIHKQGLIKSSRPL
RVLSFVAAAFFLCWSPYQVVALIATVRIRELLQGMYKEIGIAVDVTSALAFFNSCLNPMLYVFMGQDFRERLIHALPASL
ERALTEDSTQTSDTATNSTLPSAEVELQAK*

Gene Symbol:FPR1
Accession:NM_002029
Location:EXON
Amino Acid Prediction: H to H (synonymous)
Amino Acid Position: 136
Amino Acid Sequence
(Calculated using NCBI transcript definition)
METNSSLPTNISGGTPAVSAGYLFLDIITYLVFAVTFVLGVLGNGLVIWVAGFRMTHTVTTISYLNLAVADFCFTSTLPF
FMVRKAMGGHWPFGWFLCKFVFTIVDINLFGSVFLIALIALDRCVCVLHPVWTQNHRTVSLAKKVIIGPWVMALLLTLPV
IIRVTTVPGKTGTVACTFNFSPWTNDPKERINVAVAMLTVRGIIRFIIGFSAPMSIVAVSYGLIATKIHKQGLIKSSRPL
RVLSFVAAAFFLCWSPYQVVALIATVRIRELLQGMYKEIGIAVDVTSALAFFNSCLNPMLYVFMGQDFRERLIHALPASL
ERALTEDSTQTSDTATNSTLPSAEVELQAK*
.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV003075961 CLINVAR
MedGen C0017563 CLINVAR
NCBI Gene FPR1 CLINVAR
OMIM 136537 CLINVAR