RGD:405087136 Rat Genome Database

RGD:405087136 Rat Genome Database

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Variant: RGD:405087136 - Homo sapiens

RGD ID:

405087136

ClinVar ID:

CV2889670

Genic Status:

GENIC

Type:

SNV (SO:0001483)

Associated Genes:

FPR1

Reference Nucleotide:

G

Variant Nucleotide:

C

Position

Assembly	Chr	Position
GRCh37	19	52,249,896
GRCh38	19	51,746,643

JBrowse:

View Region in Genome Browser (JBrowse)

Model

HGVS Name(s)	Last Evaluated	Molecular Consequence	Clinical Significance	Trait Synonyms
LRG_146t1:c.352C>G NM_001193306.2:c.352C>G NM_002029.4:c.352C>G LRG_146:g.10255C>G More...	01/31/2024	missense variant	uncertain significance	Gingival disease

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
CV2889670	Human	gingival disease		IAGP		8554872	ClinVar Annotator: match by term: Gingival disorder	ClinVar	PMID:28492532

Gene Symbol:	FPR1
Accession:	NM_001193306
Location:	EXON
Amino Acid Prediction:	L to V (nonsynonymous)
Amino Acid Position:	118

Amino Acid Sequence (Calculated using NCBI transcript definition)
METNSSLPTNISGGTPAVSAGYLFLDIITYLVFAVTFVLGVLGNGLVIWVAGFRMTHTVTTISYLNLAVADFCFTSTLPF FMVRKAMGGHWPFGWFLCKFVFTIVDINLFGSVFLIAVIALDRCVCVLHPVWTQNHRTVSLAKKVIIGPWVMALLLTLPV IIRVTTVPGKTGTVACTFNFSPWTNDPKERINVAVAMLTVRGIIRFIIGFSAPMSIVAVSYGLIATKIHKQGLIKSSRPL RVLSFVAAAFFLCWSPYQVVALIATVRIRELLQGMYKEIGIAVDVTSALAFFNSCLNPMLYVFMGQDFRERLIHALPASL ERALTEDSTQTSDTATNSTLPSAEVELQAK*

Gene Symbol:	FPR1
Accession:	NM_002029
Location:	EXON
Amino Acid Prediction:	L to V (nonsynonymous)
Amino Acid Position:	118

Amino Acid Sequence (Calculated using NCBI transcript definition)
METNSSLPTNISGGTPAVSAGYLFLDIITYLVFAVTFVLGVLGNGLVIWVAGFRMTHTVTTISYLNLAVADFCFTSTLPF FMVRKAMGGHWPFGWFLCKFVFTIVDINLFGSVFLIAVIALDRCVCVLHPVWTQNHRTVSLAKKVIIGPWVMALLLTLPV IIRVTTVPGKTGTVACTFNFSPWTNDPKERINVAVAMLTVRGIIRFIIGFSAPMSIVAVSYGLIATKIHKQGLIKSSRPL RVLSFVAAAFFLCWSPYQVVALIATVRIRELLQGMYKEIGIAVDVTSALAFFNSCLNPMLYVFMGQDFRERLIHALPASL ERALTEDSTQTSDTATNSTLPSAEVELQAK*

ClinVar GRCh37	ClinVar GRCh38

PMID:28492532

Database	Acc Id	Source(s)
ClinVar	RCV003596803	CLINVAR
MedGen	C0017563	CLINVAR
NCBI Gene	FPR1	CLINVAR
OMIM	136537	CLINVAR