RGD:155733955 Rat Genome Database

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Variant: RGD:155733955 -  Homo sapiens

RGD ID: 155733955
ClinVar ID: CV1774368
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FPR1  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 19 52,249,659
GRCh38 19 51,746,406
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
LRG_146t1:c.589A>G
NM_001193306.2:c.589A>G
NM_002029.4:c.589A>G
LRG_146:g.10492A>G
More... 		01/01/2024 missense variant uncertain significance Gingival disease
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
CV1774368Humangingival disease  IAGP 8554872ClinVar Annotator: match by term: Gingival diseaseClinVarPMID:28492532
Gene Symbol:FPR1
Accession:NM_002029
Location:EXON
Amino Acid Prediction: M to V (nonsynonymous)
Amino Acid Position: 197
Amino Acid Sequence
(Calculated using NCBI transcript definition)
METNSSLPTNISGGTPAVSAGYLFLDIITYLVFAVTFVLGVLGNGLVIWVAGFRMTHTVTTISYLNLAVADFCFTSTLPF
FMVRKAMGGHWPFGWFLCKFVFTIVDINLFGSVFLIALIALDRCVCVLHPVWTQNHRTVSLAKKVIIGPWVMALLLTLPV
IIRVTTVPGKTGTVACTFNFSPWTNDPKERINVAVAVLTVRGIIRFIIGFSAPMSIVAVSYGLIATKIHKQGLIKSSRPL
RVLSFVAAAFFLCWSPYQVVALIATVRIRELLQGMYKEIGIAVDVTSALAFFNSCLNPMLYVFMGQDFRERLIHALPASL
ERALTEDSTQTSDTATNSTLPSAEVELQAK*

Gene Symbol:FPR1
Accession:NM_001193306
Location:EXON
Amino Acid Prediction: M to V (nonsynonymous)
Amino Acid Position: 197
Amino Acid Sequence
(Calculated using NCBI transcript definition)
METNSSLPTNISGGTPAVSAGYLFLDIITYLVFAVTFVLGVLGNGLVIWVAGFRMTHTVTTISYLNLAVADFCFTSTLPF
FMVRKAMGGHWPFGWFLCKFVFTIVDINLFGSVFLIALIALDRCVCVLHPVWTQNHRTVSLAKKVIIGPWVMALLLTLPV
IIRVTTVPGKTGTVACTFNFSPWTNDPKERINVAVAVLTVRGIIRFIIGFSAPMSIVAVSYGLIATKIHKQGLIKSSRPL
RVLSFVAAAFFLCWSPYQVVALIATVRIRELLQGMYKEIGIAVDVTSALAFFNSCLNPMLYVFMGQDFRERLIHALPASL
ERALTEDSTQTSDTATNSTLPSAEVELQAK*
.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV002301824 CLINVAR
MedGen C0017563 CLINVAR
NCBI Gene FPR1 CLINVAR
OMIM 136537 CLINVAR