Fpr1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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237 records found for search term Fpr1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
127264443	CV1106722	single nucleotide variant	NM_002029.4(FPR1):c.27G>C (p.Thr9=)	Gingival disorder [RCV002236171]	likely benign	19	51746968	51746968	Human	1	name
127313631	CV1128136	single nucleotide variant	NM_002029.4(FPR1):c.27G>A (p.Thr9=)	Gingival disorder [RCV002240295]	likely benign	19	51746968	51746968	Human	1	name
127295653	CV1128137	single nucleotide variant	NM_002029.4(FPR1):c.21C>G (p.Leu7=)	Gingival disorder [RCV002239427]	likely benign	19	51746974	51746974	Human	1	name
152077959	CV1632964	single nucleotide variant	NM_002029.4(FPR1):c.12T>C (p.Asn4=)	Gingival disorder [RCV002170174]	likely benign	19	51746983	51746983	Human	1	name
405063491	CV2993525	single nucleotide variant	NM_002029.4(FPR1):c.15C>T (p.Ser5=)	Gingival disorder [RCV003762656]	likely benign	19	51746980	51746980	Human	1	name
127279447	CV1084998	single nucleotide variant	NM_002029.4(FPR1):c.84C>T (p.Ile28=)	Gingival disorder [RCV002243107]	likely benign	19	51746911	51746911	Human	1	name
127284137	CV1106721	single nucleotide variant	NM_002029.4(FPR1):c.30C>T (p.Asn10=)	Gingival disorder [RCV002237179]	likely benign	19	51746965	51746965	Human	1	name
127312598	CV1128135	single nucleotide variant	NM_002029.4(FPR1):c.42G>A (p.Gly14=)	Gingival disorder [RCV002240290]	likely benign	19	51746953	51746953	Human	1	name
405085837	CV2872446	single nucleotide variant	NM_002029.4(FPR1):c.69C>T (p.Leu23=)	Gingival disorder [RCV003596425]	likely benign	19	51746926	51746926	Human	1	name
127239248	CV1084997	single nucleotide variant	NM_002029.4(FPR1):c.204C>T (p.Ala68=)	Gingival disorder [RCV002242933]	likely benign	19	51746791	51746791	Human	1	name
127268457	CV1106720	single nucleotide variant	NM_002029.4(FPR1):c.189T>C (p.Ser63=)	Gingival disorder [RCV002236354]	likely benign	19	51746806	51746806	Human	1	name
152122750	CV1587130	single nucleotide variant	NM_002029.4(FPR1):c.132C>T (p.Asn44=)	Gingival disorder [RCV002135920]	likely benign	19	51746863	51746863	Human	1	name
152106225	CV1609013	single nucleotide variant	NM_002029.4(FPR1):c.156A>T (p.Gly52=)	Gingival disorder [RCV002096200]	likely benign	19	51746839	51746839	Human	1	name
156372659	CV2127659	single nucleotide variant	NM_002029.4(FPR1):c.279C>T (p.Phe93=)	Gingival disorder [RCV002942460]	likely benign	19	51746716	51746716	Human	1	name
405085958	CV2875964	single nucleotide variant	NM_002029.4(FPR1):c.17C>T (p.Ser6Phe)	Gingival disorder [RCV003596432]	likely benign	19	51746978	51746978	Human	1	name
405089432	CV2908729	single nucleotide variant	NM_002029.4(FPR1):c.144C>T (p.Ile48=)	Gingival disorder [RCV003596983]	likely benign	19	51746851	51746851	Human	1	name
405089391	CV2919420	single nucleotide variant	NM_002029.4(FPR1):c.258C>T (p.Ala86=)	Gingival disorder [RCV003596984]	likely benign	19	51746737	51746737	Human	1	name
597968239	CV3820869	single nucleotide variant	NM_002029.4(FPR1):c.17C>G (p.Ser6Cys)	Gingival disorder [RCV005165710]	uncertain significance	19	51746978	51746978	Human	1	name
597972214	CV3829519	single nucleotide variant	NM_002029.4(FPR1):c.171C>T (p.His57=)	Gingival disorder [RCV005167306]	likely benign	19	51746824	51746824	Human	1	name
597885510	CV3838546	single nucleotide variant	NM_002029.4(FPR1):c.186C>T (p.Ile62=)	Gingival disorder [RCV005178818]	likely benign	19	51746809	51746809	Human	1	name
13467846	CV470764	single nucleotide variant	NM_002029.4(FPR1):c.26C>T (p.Thr9Met)	Gingival disorder [RCV002231220]\|not provided [RCV001703188]	likely benign	19	51746969	51746969	Human	1	name
13501562	CV471280	single nucleotide variant	NM_002029.4(FPR1):c.177C>T (p.Val59=)	Gingival disorder [RCV002231219]\|not provided [RCV004717648]	benign	19	51746818	51746818	Human	1	name
13613298	CV533878	single nucleotide variant	NM_002029.4(FPR1):c.117C>T (p.Leu39=)	Gingival disorder [RCV002234400]\|not provided [RCV004717692]	benign	19	51746878	51746878	Human	1	name
126769228	CV1013922	single nucleotide variant	NM_002029.4(FPR1):c.80T>A (p.Ile27Asn)	Gingival disorder [RCV002242267]	uncertain significance	19	51746915	51746915	Human	1	name
127270087	CV1084991	single nucleotide variant	NM_002029.4(FPR1):c.969C>T (p.Ala323=)	Gingival disorder [RCV002242972]	likely benign	19	51746026	51746026	Human	1	name
127250213	CV1084992	single nucleotide variant	NM_002029.4(FPR1):c.726C>T (p.Val242=)	Gingival disorder [RCV002243024]	likely benign	19	51746269	51746269	Human	1	name
127243818	CV1084993	single nucleotide variant	NM_002029.4(FPR1):c.618C>T (p.Phe206=)	Gingival disorder [RCV002243131]	likely benign	19	51746377	51746377	Human	1	name
127246641	CV1084995	single nucleotide variant	NM_002029.4(FPR1):c.453G>A (p.Val151=)	Gingival disorder [RCV002242938]	likely benign	19	51746542	51746542	Human	1	name
127280060	CV1084996	single nucleotide variant	NM_002029.4(FPR1):c.378C>T (p.Cys126=)	Gingival disorder [RCV002243057]	likely benign	19	51746617	51746617	Human	1	name
127280377	CV1106717	single nucleotide variant	NM_002029.4(FPR1):c.474G>A (p.Leu158=)	Gingival disorder [RCV002237162]	likely benign	19	51746521	51746521	Human	1	name
127271222	CV1106719	single nucleotide variant	NM_002029.4(FPR1):c.330C>T (p.Phe110=)	Gingival disorder [RCV002236360]	likely benign	19	51746665	51746665	Human	1	name
127314749	CV1128130	single nucleotide variant	NM_002029.4(FPR1):c.957T>C (p.Ser319=)	Gingival disorder [RCV002240275]	likely benign	19	51746038	51746038	Human	1	name
127335918	CV1128131	single nucleotide variant	NM_002029.4(FPR1):c.954C>G (p.Ala318=)	Gingival disorder [RCV002240596]	likely benign	19	51746041	51746041	Human	1	name
127330091	CV1128132	single nucleotide variant	NM_002029.4(FPR1):c.738C>T (p.Val246=)	Gingival disorder [RCV002240447]	likely benign	19	51746257	51746257	Human	1	name
127300312	CV1128133	single nucleotide variant	NM_002029.4(FPR1):c.390A>G (p.Pro130=)	Gingival disorder [RCV002240269]	likely benign	19	51746605	51746605	Human	1	name
127295762	CV1128134	single nucleotide variant	NM_002029.4(FPR1):c.381C>T (p.Val127=)	Gingival disorder [RCV002240663]	likely benign	19	51746614	51746614	Human	1	name
127288623	CV1149067	single nucleotide variant	NM_002029.4(FPR1):c.942C>T (p.His314=)	Gingival disorder [RCV002240883]	likely benign	19	51746053	51746053	Human	1	name
127328974	CV1149068	single nucleotide variant	NM_002029.4(FPR1):c.858A>G (p.Thr286=)	FPR1-related disorder [RCV003948420]\|Gingival disorder [RCV002240708]	likely benign	19	51746137	51746137	Human	1	name , trait , alternate_id
127301613	CV1149069	single nucleotide variant	NM_002029.4(FPR1):c.639C>T (p.Pro213=)	Gingival disorder [RCV002241020]\|not provided [RCV004704627]	likely benign	19	51746356	51746356	Human	1	name
127324955	CV1149070	single nucleotide variant	NM_002029.4(FPR1):c.564A>G (p.Lys188=)	Gingival disorder [RCV002240699]	likely benign	19	51746431	51746431	Human	1	name
127319029	CV1149071	single nucleotide variant	NM_002029.4(FPR1):c.513G>A (p.Thr171=)	Gingival disorder [RCV002241173]	likely benign	19	51746482	51746482	Human	1	name
127308419	CV1149072	single nucleotide variant	NM_002029.4(FPR1):c.472T>C (p.Leu158=)	Gingival disorder [RCV002241028]	likely benign	19	51746523	51746523	Human	1	name
127335144	CV1149073	single nucleotide variant	NM_002029.4(FPR1):c.300C>T (p.Phe100=)	Gingival disorder [RCV002241006]	likely benign	19	51746695	51746695	Human	1	name
127310220	CV1158642	single nucleotide variant	NM_002029.4(FPR1):c.576T>C (p.Asn192=)	Gingival disorder [RCV002241361]\|not provided [RCV001824979]	benign\|not provided	19	51746419	51746419	Human	1	name
152062216	CV1532983	single nucleotide variant	NM_002029.4(FPR1):c.447C>T (p.Pro149=)	Gingival disorder [RCV002090389]	likely benign	19	51746548	51746548	Human	1	name
152151219	CV1550085	single nucleotide variant	NM_002029.4(FPR1):c.519A>T (p.Thr173=)	Gingival disorder [RCV002201995]	likely benign	19	51746476	51746476	Human	1	name
152117671	CV1556301	single nucleotide variant	NM_002029.4(FPR1):c.543G>A (p.Ser181=)	Gingival disorder [RCV002216355]	likely benign	19	51746452	51746452	Human	1	name
152067594	CV1566893	single nucleotide variant	NM_002029.4(FPR1):c.555C>T (p.Asn185=)	Gingival disorder [RCV002091140]	likely benign	19	51746440	51746440	Human	1	name
152077071	CV1592116	single nucleotide variant	NM_002029.4(FPR1):c.528C>T (p.Cys176=)	Gingival disorder [RCV002112250]	likely benign	19	51746467	51746467	Human	1	name
152044992	CV1614056	single nucleotide variant	NM_002029.4(FPR1):c.486T>C (p.Ile162=)	Gingival disorder [RCV002166174]	likely benign	19	51746509	51746509	Human	1	name
152153915	CV1643525	single nucleotide variant	NM_002029.4(FPR1):c.339C>A (p.Val113=)	Gingival disorder [RCV002122150]	likely benign	19	51746656	51746656	Human	1	name
152079723	CV1663476	single nucleotide variant	NM_002029.4(FPR1):c.414C>T (p.Thr138=)	Gingival disorder [RCV002149147]	likely benign	19	51746581	51746581	Human	1	name
152099318	CV1663946	single nucleotide variant	NM_002029.4(FPR1):c.975C>G (p.Thr325=)	Gingival disorder [RCV002078779]	likely benign	19	51746020	51746020	Human	1	name
155987616	CV1884142	single nucleotide variant	NM_002029.4(FPR1):c.408C>T (p.His136=)	Gingival disorder [RCV003075961]	likely benign	19	51746587	51746587	Human	1	name
156444860	CV1948905	single nucleotide variant	NM_002029.4(FPR1):c.465C>T (p.Leu155=)	Gingival disorder [RCV003115790]	likely benign	19	51746530	51746530	Human	1	name
156131629	CV2036589	single nucleotide variant	NM_002029.4(FPR1):c.648C>T (p.Ile216=)	Gingival disorder [RCV002786194]	likely benign	19	51746347	51746347	Human	1	name
155939159	CV2041590	single nucleotide variant	NM_002029.4(FPR1):c.723G>T (p.Arg241=)	Gingival disorder [RCV002775075]	likely benign	19	51746272	51746272	Human	1	name
156109115	CV2058142	duplication	NM_002029.4(FPR1):c.211dup (p.Asp71fs)	Gingival disorder [RCV002824851]	uncertain significance	19	51746783	51746784	Human	1	name
156328544	CV2064989	single nucleotide variant	NM_002029.4(FPR1):c.960G>A (p.Leu320=)	Gingival disorder [RCV002835158]	likely benign	19	51746035	51746035	Human	1	name
155914173	CV2077896	single nucleotide variant	NM_002029.4(FPR1):c.876C>T (p.Phe292=)	Gingival disorder [RCV002858710]	likely benign	19	51746119	51746119	Human	1	name
155995395	CV2095723	single nucleotide variant	NM_002029.4(FPR1):c.52G>A (p.Val18Ile)	Gingival disorder [RCV002908358]	uncertain significance	19	51746943	51746943	Human	1	name
156388676	CV2122236	single nucleotide variant	NM_002029.4(FPR1):c.726C>A (p.Val242=)	FPR1-related disorder [RCV003898635]\|Gingival disorder [RCV002943690]	likely benign	19	51746269	51746269	Human	1	name , trait , alternate_id
156023389	CV2139010	single nucleotide variant	NM_002029.4(FPR1):c.696C>G (p.Gly232=)	Gingival disorder [RCV002998791]	likely benign	19	51746299	51746299	Human	1	name
405086767	CV2888931	single nucleotide variant	NM_002029.4(FPR1):c.444G>T (p.Gly148=)	Gingival disorder [RCV003596768]	likely benign	19	51746551	51746551	Human	1	name
405090969	CV2914131	single nucleotide variant	NM_002029.4(FPR1):c.77A>C (p.Asp26Ala)	Gingival disorder [RCV003597014]	uncertain significance	19	51746918	51746918	Human	1	name
405059055	CV2942456	single nucleotide variant	NM_002029.4(FPR1):c.44C>A (p.Thr15Lys)	Gingival disorder [RCV003762275]	uncertain significance	19	51746951	51746951	Human	1	name
405059658	CV2958545	single nucleotide variant	NM_002029.4(FPR1):c.56C>G (p.Ser19Cys)	Gingival disorder [RCV003762326]	uncertain significance	19	51746939	51746939	Human	1	name
405059970	CV2962240	single nucleotide variant	NM_002029.4(FPR1):c.624T>C (p.Ile208=)	Gingival disorder [RCV003762351]	likely benign	19	51746371	51746371	Human	1	name
405068686	CV3035721	single nucleotide variant	NM_002029.4(FPR1):c.918G>A (p.Gln306=)	Gingival disorder [RCV003763506]	likely benign	19	51746077	51746077	Human	1	name
405072892	CV3045921	single nucleotide variant	NM_002029.4(FPR1):c.333A>G (p.Gly111=)	Gingival disorder [RCV003764224]	likely benign	19	51746662	51746662	Human	1	name
405143036	CV3155668	single nucleotide variant	NM_002029.4(FPR1):c.77A>G (p.Asp26Gly)	Gingival disorder [RCV003855710]	uncertain significance	19	51746918	51746918	Human	1	name
405246913	CV3158572	single nucleotide variant	NM_002029.4(FPR1):c.405C>T (p.Asn135=)	Gingival disorder [RCV003868914]	likely benign	19	51746590	51746590	Human	1	name
597846306	CV3736441	single nucleotide variant	NM_002029.4(FPR1):c.951C>T (p.Pro317=)	Gingival disorder [RCV005060019]	likely benign	19	51746044	51746044	Human	1	name
597831106	CV3743789	single nucleotide variant	NM_002029.4(FPR1):c.891C>T (p.Asn297=)	Gingival disorder [RCV005062606]	likely benign	19	51746104	51746104	Human	1	name
597966971	CV3751714	single nucleotide variant	NM_002029.4(FPR1):c.382C>T (p.Leu128=)	Gingival disorder [RCV005083084]	likely benign	19	51746613	51746613	Human	1	name
597962692	CV3791505	single nucleotide variant	NM_002029.4(FPR1):c.62G>C (p.Gly21Ala)	Gingival disorder [RCV005139259]	uncertain significance	19	51746933	51746933	Human	1	name
597967272	CV3794460	single nucleotide variant	NM_002029.4(FPR1):c.519A>G (p.Thr173=)	Gingival disorder [RCV005140636]	likely benign	19	51746476	51746476	Human	1	name
12896495	CV390319	single nucleotide variant	NM_002029.4(FPR1):c.32T>C (p.Ile11Thr)	Gingival disorder [RCV002230304]\|not provided [RCV001824775]\|not specified [RCV000455423]	benign\|not provided	19	51746963	51746963	Human	2	name
12896495	CV390319	single nucleotide variant	NM_002029.4(FPR1):c.32T>C (p.Ile11Thr)	Gingival disorder [RCV002230304]\|not provided [RCV001824775]\|not specified [RCV000455423]	benign\|not provided	19	51746963	51746964	Human	2	name
12895897	CV390431	single nucleotide variant	NM_002029.4(FPR1):c.993C>T (p.Thr331=)	Gingival disorder [RCV002230301]\|not provided [RCV004717605]\|not specified [RCV000454608]	benign	19	51746002	51746002	Human	1	name
12896954	CV390462	single nucleotide variant	NM_002029.4(FPR1):c.546C>A (p.Pro182=)	Gingival disorder [RCV002230303]\|not provided [RCV001824773]\|not specified [RCV000456043]	benign\|not provided	19	51746449	51746449	Human	1	name
13498714	CV470757	single nucleotide variant	NM_002029.4(FPR1):c.306T>C (p.Phe102=)	Gingival disorder [RCV002231221]\|not provided [RCV004717649]	benign	19	51746689	51746689	Human	1	name
13464942	CV471279	single nucleotide variant	NM_002029.4(FPR1):c.348C>T (p.Ile116=)	Gingival disorder [RCV002231222]\|not provided [RCV004717650]	benign	19	51746647	51746647	Human	1	name
13613294	CV533874	single nucleotide variant	NM_002029.4(FPR1):c.645C>T (p.Ser215=)	FPR1-related disorder [RCV003905689]\|Gingival disorder [RCV002234401]\|not provided [RCV004717693]	benign	19	51746350	51746350	Human	1	name , trait , alternate_id
15178202	CV728381	single nucleotide variant	NM_002029.4(FPR1):c.822C>T (p.Gly274=)	FPR1-related disorder [RCV003930635]\|Gingival disorder [RCV002236048]\|not provided [RCV004717727]	benign\|likely benign	19	51746173	51746173	Human	1	name , trait , alternate_id
15194970	CV728382	single nucleotide variant	NM_002029.4(FPR1):c.744A>C (p.Ala248=)	Gingival disorder [RCV002235489]\|not provided [RCV004704272]	likely benign	19	51746251	51746251	Human	1	name
15148699	CV742098	single nucleotide variant	NM_002029.4(FPR1):c.582C>T (p.Ala194=)	Gingival disorder [RCV002235612]	likely benign	19	51746413	51746413	Human	1	name
15141685	CV772885	single nucleotide variant	NM_002029.4(FPR1):c.705G>A (p.Lys235=)	Gingival disorder [RCV002235823]	likely benign	19	51746290	51746290	Human	1	name
8628386	CV83530	single nucleotide variant	NM_002029.3(FPR1):c.516G>A (p.Gly172=)	Malignant melanoma [RCV000063611]	not provided	19	51746479	51746479	Human		name
26884610	CV848031	single nucleotide variant	NM_002029.4(FPR1):c.934C>T (p.Leu312=)	Gingival disorder [RCV002240323]	likely benign\|uncertain significance	19	51746061	51746061	Human	1	name
26918600	CV848040	single nucleotide variant	NM_002029.4(FPR1):c.79A>G (p.Ile27Val)	Gingival disorder [RCV002239358]	uncertain significance	19	51746916	51746916	Human	1	name
26915982	CV848041	single nucleotide variant	NM_002029.4(FPR1):c.40G>A (p.Gly14Arg)	Gingival disorder [RCV002239298]	uncertain significance	19	51746955	51746955	Human	1	name
38481974	CV938843	single nucleotide variant	NM_002029.4(FPR1):c.654T>A (p.Ala218=)	Gingival disorder [RCV002240973]	likely benign\|uncertain significance	19	51746341	51746341	Human	1	name
126745642	CV1013921	single nucleotide variant	NM_002029.4(FPR1):c.121G>A (p.Val41Ile)	Gingival disorder [RCV002242286]	uncertain significance	19	51746874	51746874	Human	1	name
127321324	CV1128129	single nucleotide variant	NM_002029.4(FPR1):c.1044G>A (p.Gln348=)	Gingival disorder [RCV002240430]	likely benign	19	51745951	51745951	Human	1	name
151732901	CV1355664	single nucleotide variant	NM_002029.4(FPR1):c.272G>A (p.Trp91Ter)	Gingival disorder [RCV001984392]	uncertain significance	19	51746723	51746723	Human	1	name
151811575	CV1371410	single nucleotide variant	NM_002029.4(FPR1):c.275C>T (p.Pro92Leu)	Gingival disorder [RCV001933254]	uncertain significance	19	51746720	51746720	Human	1	name
151860292	CV1389820	single nucleotide variant	NM_002029.4(FPR1):c.161G>A (p.Arg54Gln)	Gingival disorder [RCV001905188]	uncertain significance	19	51746834	51746834	Human	1	name
151793947	CV1390374	single nucleotide variant	NM_002029.4(FPR1):c.139G>T (p.Val47Leu)	Gingival disorder [RCV001952305]	uncertain significance	19	51746856	51746856	Human	1	name
151730213	CV1505463	single nucleotide variant	NM_002029.4(FPR1):c.257C>T (p.Ala86Val)	Gingival disorder [RCV002021212]	uncertain significance	19	51746738	51746738	Human	1	name
155683090	CV1776796	single nucleotide variant	NM_002029.4(FPR1):c.144C>G (p.Ile48Met)	Gingival disorder [RCV002298332]	uncertain significance	19	51746851	51746851	Human	1	name
156124171	CV1892774	single nucleotide variant	NM_002029.4(FPR1):c.268C>T (p.His90Tyr)	Gingival disorder [RCV003081568]	uncertain significance	19	51746727	51746727	Human	1	name
156337578	CV1902326	single nucleotide variant	NM_002029.4(FPR1):c.185T>A (p.Ile62Asn)	Gingival disorder [RCV003090161]	uncertain significance	19	51746810	51746810	Human	1	name
156418481	CV1922217	single nucleotide variant	NM_002029.4(FPR1):c.284G>T (p.Trp95Leu)	Gingival disorder [RCV002611677]	uncertain significance	19	51746711	51746711	Human	1	name
156441767	CV1941421	single nucleotide variant	NM_002029.4(FPR1):c.133G>A (p.Gly45Arg)	Gingival disorder [RCV003112099]	uncertain significance	19	51746862	51746862	Human	1	name
156129521	CV2036494	single nucleotide variant	NM_002029.4(FPR1):c.118G>A (p.Gly40Arg)	Gingival disorder [RCV002786114]	uncertain significance	19	51746877	51746877	Human	1	name
156339699	CV2106828	single nucleotide variant	NM_002029.4(FPR1):c.245T>C (p.Met82Thr)	Gingival disorder [RCV002938829]	uncertain significance	19	51746750	51746750	Human	1	name
156017161	CV2120624	single nucleotide variant	NM_002029.4(FPR1):c.1008C>A (p.Thr336=)	Gingival disorder [RCV002975965]	likely benign	19	51745987	51745987	Human	1	name
156250083	CV2169044	single nucleotide variant	NM_002029.4(FPR1):c.1008C>T (p.Thr336=)	Gingival disorder [RCV003026308]	likely benign	19	51745987	51745987	Human	1	name
156228091	CV2234864	single nucleotide variant	NM_002029.4(FPR1):c.283T>G (p.Trp95Gly)	not specified [RCV004113082]	uncertain significance	19	51746712	51746712	Human		name
405084967	CV2868272	single nucleotide variant	NM_002029.4(FPR1):c.208G>A (p.Ala70Thr)	Gingival disorder [RCV003596407]	uncertain significance	19	51746787	51746787	Human	1	name
405069068	CV3039449	single nucleotide variant	NM_002029.4(FPR1):c.244A>G (p.Met82Val)	Gingival disorder [RCV003763531]	uncertain significance	19	51746751	51746751	Human	1	name
405199425	CV3147169	single nucleotide variant	NM_002029.4(FPR1):c.139G>A (p.Val47Met)	Gingival disorder [RCV003844329]	uncertain significance	19	51746856	51746856	Human	1	name
405286341	CV3192138	single nucleotide variant	NM_002029.4(FPR1):c.1038G>A (p.Glu346=)	FPR1-related disorder [RCV003924053]	likely benign	19	51745957	51745957	Human		name , trait , alternate_id
597957713	CV3848933	single nucleotide variant	NM_002029.4(FPR1):c.1047A>G (p.Ala349=)	Gingival disorder [RCV005191934]	likely benign	19	51745948	51745948	Human	1	name
597897694	CV3854417	single nucleotide variant	NM_002029.4(FPR1):c.136C>G (p.Leu46Val)	Gingival disorder [RCV005201524]	uncertain significance	19	51746859	51746859	Human	1	name
13613331	CV533441	single nucleotide variant	NM_002029.4(FPR1):c.289C>A (p.Leu97Met)	FPR1-related disorder [RCV003935753]\|Gingival disorder [RCV002233924]\|not provided [RCV004717694]	benign	19	51746706	51746706	Human	1	name , trait , alternate_id
14719961	CV648444	single nucleotide variant	NM_002029.4(FPR1):c.274C>A (p.Pro92Thr)	Gingival disorder [RCV002235030]\|not specified [RCV004028779]	uncertain significance	19	51746721	51746721	Human	1	name
14730133	CV648445	single nucleotide variant	NM_002029.4(FPR1):c.205G>A (p.Val69Met)	Gingival disorder [RCV002235094]\|not specified [RCV004028907]	uncertain significance	19	51746790	51746790	Human	1	name
14730627	CV648446	single nucleotide variant	NM_002029.4(FPR1):c.198C>A (p.Asn66Lys)	Gingival disorder [RCV003596609]	uncertain significance	19	51746797	51746797	Human	1	name
38493089	CV958728	single nucleotide variant	NM_002029.4(FPR1):c.160C>T (p.Arg54Trp)	Gingival disorder [RCV002241628]	uncertain significance	19	51746835	51746835	Human	1	name
126751281	CV1013920	single nucleotide variant	NM_002029.4(FPR1):c.824T>C (p.Met275Thr)	Gingival disorder [RCV002242167]\|not specified [RCV005340794]	uncertain significance	19	51746171	51746171	Human	1	name
126756358	CV1034483	single nucleotide variant	NM_002029.4(FPR1):c.926G>A (p.Arg309Gln)	Gingival disorder [RCV002242470]	uncertain significance	19	51746069	51746069	Human	1	name
126922765	CV1051496	single nucleotide variant	NM_002029.4(FPR1):c.407A>C (p.His136Pro)	Gingival disorder [RCV002242582]	uncertain significance	19	51746588	51746588	Human	1	name
127239212	CV1084994	single nucleotide variant	NM_002029.4(FPR1):c.553A>G (p.Asn185Asp)	Gingival disorder [RCV002243074]	likely benign	19	51746442	51746442	Human	1	name
127275847	CV1106718	single nucleotide variant	NM_002029.4(FPR1):c.439A>T (p.Ile147Phe)	Gingival disorder [RCV002237151]	likely benign	19	51746556	51746556	Human	1	name
151890920	CV1346818	single nucleotide variant	NM_002029.4(FPR1):c.301G>A (p.Val101Ile)	Gingival disorder [RCV002038943]	uncertain significance	19	51746694	51746694	Human	1	name
151858234	CV1360133	single nucleotide variant	NM_002029.4(FPR1):c.476C>G (p.Pro159Arg)	Gingival disorder [RCV001904956]	uncertain significance	19	51746519	51746519	Human	1	name
151834507	CV1369980	single nucleotide variant	NM_002029.4(FPR1):c.466C>T (p.Leu156Phe)	Gingival disorder [RCV001920826]	uncertain significance	19	51746529	51746529	Human	1	name
151859537	CV1398462	single nucleotide variant	NM_002029.4(FPR1):c.758G>T (p.Cys253Phe)	Gingival disorder [RCV002017587]	uncertain significance	19	51746237	51746237	Human	1	name
151743620	CV1404517	single nucleotide variant	NM_002029.4(FPR1):c.487C>T (p.Arg163Cys)	Gingival disorder [RCV002022574]	uncertain significance	19	51746508	51746508	Human	1	name
151741091	CV1404816	single nucleotide variant	NM_002029.4(FPR1):c.623T>C (p.Ile208Thr)	Gingival disorder [RCV001947108]	uncertain significance	19	51746372	51746372	Human	1	name
151834370	CV1413055	single nucleotide variant	NM_002029.4(FPR1):c.652G>T (p.Ala218Ser)	Gingival disorder [RCV002014626]	uncertain significance	19	51746343	51746343	Human	1	name
151837574	CV1417020	single nucleotide variant	NM_002029.4(FPR1):c.851A>G (p.Asp284Gly)	Gingival disorder [RCV002014956]	uncertain significance	19	51746144	51746144	Human	1	name
151885663	CV1418105	single nucleotide variant	NM_002029.4(FPR1):c.556G>A (p.Asp186Asn)	Gingival disorder [RCV001887401]	uncertain significance	19	51746439	51746439	Human	1	name
151850055	CV1427867	single nucleotide variant	NM_002029.4(FPR1):c.367C>T (p.Arg123Cys)	Gingival disorder [RCV001922654]	uncertain significance	19	51746628	51746628	Human	1	name
151802788	CV1437682	single nucleotide variant	NM_002029.4(FPR1):c.821G>C (p.Gly274Ala)	Gingival disorder [RCV001899217]	uncertain significance	19	51746174	51746174	Human	1	name
151827521	CV1437833	single nucleotide variant	NM_002029.4(FPR1):c.445C>T (p.Pro149Ser)	Gingival disorder [RCV001920168]\|not specified [RCV004616846]	uncertain significance	19	51746550	51746550	Human	1	name
151884498	CV1452667	single nucleotide variant	NM_002029.4(FPR1):c.707C>G (p.Ser236Cys)	Gingival disorder [RCV002037563]	uncertain significance	19	51746288	51746288	Human	1	name
151715753	CV1472663	single nucleotide variant	NM_002029.4(FPR1):c.456G>A (p.Met152Ile)	Gingival disorder [RCV002039306]	uncertain significance	19	51746539	51746539	Human	1	name
151866985	CV1474004	single nucleotide variant	NM_002029.4(FPR1):c.512C>T (p.Thr171Met)	Gingival disorder [RCV001906002]\|not specified [RCV004041418]	likely benign\|uncertain significance	19	51746483	51746483	Human	1	name
9686878	CV171639	single nucleotide variant	NM_002029.4(FPR1):c.772C>T (p.Gln258Ter)	Prostate cancer [RCV000149096]	uncertain significance	19	51746223	51746223	Human	2	name
155733955	CV1774368	single nucleotide variant	NM_002029.4(FPR1):c.589A>G (p.Met197Val)	Gingival disorder [RCV002301824]	uncertain significance	19	51746406	51746406	Human	1	name
156284069	CV1877287	single nucleotide variant	NM_002029.4(FPR1):c.982T>C (p.Ser328Pro)	Gingival disorder [RCV003068619]\|not specified [RCV004070451]	uncertain significance	19	51746013	51746013	Human	1	name
156084461	CV1898861	single nucleotide variant	NM_002029.4(FPR1):c.914G>T (p.Gly305Val)	Gingival disorder [RCV003079987]	uncertain significance	19	51746081	51746081	Human	1	name
156362856	CV1905222	single nucleotide variant	NM_002029.4(FPR1):c.591G>A (p.Met197Ile)	Gingival disorder [RCV002602621]\|not specified [RCV004068779]	uncertain significance	19	51746404	51746404	Human	1	name
156345200	CV1907810	single nucleotide variant	NM_002029.4(FPR1):c.349G>A (p.Ala117Thr)	Gingival disorder [RCV003090594]	uncertain significance	19	51746646	51746646	Human	1	name
156062035	CV1925685	single nucleotide variant	NM_002029.4(FPR1):c.506G>A (p.Gly169Asp)	Gingival disorder [RCV002620980]	uncertain significance	19	51746489	51746489	Human	1	name
156444397	CV1938259	single nucleotide variant	NM_002029.4(FPR1):c.682A>T (p.Ile228Phe)	Gingival disorder [RCV003115321]	uncertain significance	19	51746313	51746313	Human	1	name
156007898	CV2042524	single nucleotide variant	NM_002029.4(FPR1):c.775G>A (p.Val259Met)	Gingival disorder [RCV002794937]	uncertain significance	19	51746220	51746220	Human	1	name
156342860	CV2055509	single nucleotide variant	NM_002029.4(FPR1):c.752T>A (p.Phe251Tyr)	Gingival disorder [RCV002811294]	uncertain significance	19	51746243	51746243	Human	1	name
156352086	CV2118684	single nucleotide variant	NM_002029.4(FPR1):c.646A>G (p.Ile216Val)	Gingival disorder [RCV002966373]\|not specified [RCV004068127]	uncertain significance	19	51746349	51746349	Human	1	name
156216591	CV2128016	single nucleotide variant	NM_002029.4(FPR1):c.415G>A (p.Val139Met)	Gingival disorder [RCV002957971]	uncertain significance	19	51746580	51746580	Human	1	name
155972922	CV2135862	single nucleotide variant	NM_002029.4(FPR1):c.541T>C (p.Ser181Pro)	Gingival disorder [RCV002995714]	uncertain significance	19	51746454	51746454	Human	1	name
155955385	CV2143955	single nucleotide variant	NM_002029.4(FPR1):c.583G>A (p.Val195Ile)	Gingival disorder [RCV002994866]	uncertain significance	19	51746412	51746412	Human	1	name
156021574	CV2226800	single nucleotide variant	NM_002029.4(FPR1):c.902A>G (p.Tyr301Cys)	not specified [RCV004102008]	uncertain significance	19	51746093	51746093	Human		name
155918930	CV2279317	single nucleotide variant	NM_002029.4(FPR1):c.470C>T (p.Thr157Ile)	not specified [RCV004139833]	uncertain significance	19	51746525	51746525	Human		name
329846343	CV2524666	single nucleotide variant	NM_002029.4(FPR1):c.443G>A (p.Gly148Glu)	not provided [RCV003228149]	uncertain significance	19	51746552	51746552	Human		name
401749347	CV2694624	single nucleotide variant	NM_002029.4(FPR1):c.380T>C (p.Val127Ala)	not specified [RCV004298738]	uncertain significance	19	51746615	51746615	Human		name
401762652	CV2711071	single nucleotide variant	NM_002029.4(FPR1):c.622A>T (p.Ile208Phe)	not specified [RCV004310763]	uncertain significance	19	51746373	51746373	Human		name
405086091	CV2869560	single nucleotide variant	NM_002029.4(FPR1):c.739G>A (p.Ala247Thr)	Gingival disorder [RCV003596451]	uncertain significance	19	51746256	51746256	Human	1	name
405087136	CV2889670	single nucleotide variant	NM_002029.4(FPR1):c.352C>G (p.Leu118Val)	Gingival disorder [RCV003596803]	uncertain significance	19	51746643	51746643	Human	1	name
405061394	CV2966556	single nucleotide variant	NM_002029.4(FPR1):c.641T>G (p.Met214Arg)	Gingival disorder [RCV003762474]	uncertain significance	19	51746354	51746354	Human	1	name
405061951	CV2978027	single nucleotide variant	NM_002029.4(FPR1):c.642G>A (p.Met214Ile)	Gingival disorder [RCV003762520]	uncertain significance	19	51746353	51746353	Human	1	name
405067396	CV3021919	single nucleotide variant	NM_002029.4(FPR1):c.829A>C (p.Lys277Gln)	Gingival disorder [RCV003763356]	uncertain significance	19	51746166	51746166	Human	1	name
405067953	CV3031148	single nucleotide variant	NM_002029.4(FPR1):c.443G>C (p.Gly148Ala)	Gingival disorder [RCV003763457]	uncertain significance	19	51746552	51746552	Human	1	name
405068741	CV3040315	single nucleotide variant	NM_002029.4(FPR1):c.410G>A (p.Arg137His)	Gingival disorder [RCV003763476]	uncertain significance	19	51746585	51746585	Human	1	name
405068812	CV3041590	single nucleotide variant	NM_002029.4(FPR1):c.484A>G (p.Ile162Val)	Gingival disorder [RCV003763515]	uncertain significance	19	51746511	51746511	Human	1	name
405070753	CV3050722	single nucleotide variant	NM_002029.4(FPR1):c.841A>G (p.Ile281Val)	Gingival disorder [RCV003763643]	uncertain significance	19	51746154	51746154	Human	1	name
405075279	CV3073892	single nucleotide variant	NM_002029.4(FPR1):c.524C>T (p.Ala175Val)	FPR1-related disorder [RCV004757611]\|Gingival disorder [RCV003764389]	uncertain significance	19	51746471	51746471	Human	1	name , trait , alternate_id
405075214	CV3078981	single nucleotide variant	NM_002029.4(FPR1):c.853G>A (p.Val285Met)	Gingival disorder [RCV003764384]	uncertain significance	19	51746142	51746142	Human	1	name
405162204	CV3153113	single nucleotide variant	NM_002029.4(FPR1):c.548G>A (p.Trp183Ter)	Gingival disorder [RCV003840848]	uncertain significance	19	51746447	51746447	Human	1	name
405219166	CV3154221	single nucleotide variant	NM_002029.4(FPR1):c.897G>A (p.Met299Ile)	Gingival disorder [RCV003846913]	uncertain significance	19	51746098	51746098	Human	1	name
402471727	CV3171625	single nucleotide variant	NM_002029.4(FPR1):c.436A>G (p.Ile146Val)	Gingival disorder [RCV003874409]\|not specified [RCV004369630]	uncertain significance	19	51746559	51746559	Human	1	name
402471789	CV3171637	single nucleotide variant	NM_002029.4(FPR1):c.554A>G (p.Asn185Ser)	Gingival disorder [RCV003874421]	uncertain significance	19	51746441	51746441	Human	1	name
405252344	CV3177919	single nucleotide variant	NM_002029.4(FPR1):c.346A>T (p.Ile116Phe)	Gingival disorder [RCV003870699]	uncertain significance	19	51746649	51746649	Human	1	name
404999838	CV3183593	single nucleotide variant	NM_002029.4(FPR1):c.350C>T (p.Ala117Val)	Gingival disorder [RCV003882470]	uncertain significance	19	51746645	51746645	Human	1	name
597970136	CV3750125	single nucleotide variant	NM_002029.4(FPR1):c.912G>A (p.Met304Ile)	Gingival disorder [RCV005084066]	uncertain significance	19	51746083	51746083	Human	1	name
597938897	CV3760181	single nucleotide variant	NM_002029.4(FPR1):c.665G>A (p.Gly222Glu)	Gingival disorder [RCV005077105]	uncertain significance	19	51746330	51746330	Human	1	name
597849410	CV3761674	single nucleotide variant	NM_002029.4(FPR1):c.481A>G (p.Ile161Val)	Gingival disorder [RCV005087770]	uncertain significance	19	51746514	51746514	Human	1	name
597949662	CV3772385	single nucleotide variant	NM_002029.4(FPR1):c.331G>C (p.Gly111Arg)	Gingival disorder [RCV005120704]	uncertain significance	19	51746664	51746664	Human	1	name
597928646	CV3779794	single nucleotide variant	NM_002029.4(FPR1):c.730T>C (p.Ser244Pro)	Gingival disorder [RCV005116323]	uncertain significance	19	51746265	51746265	Human	1	name
597952486	CV3815791	single nucleotide variant	NM_002029.4(FPR1):c.766C>T (p.Pro256Ser)	Gingival disorder [RCV005161544]	uncertain significance	19	51746229	51746229	Human	1	name
597862080	CV3817723	single nucleotide variant	NM_002029.4(FPR1):c.539T>A (p.Phe180Tyr)	Gingival disorder [RCV005146909]	uncertain significance	19	51746456	51746456	Human	1	name
597875362	CV3829678	single nucleotide variant	NM_002029.4(FPR1):c.635C>T (p.Ala212Val)	Gingival disorder [RCV005177386]	uncertain significance	19	51746360	51746360	Human	1	name
597956096	CV3838134	single nucleotide variant	NM_002029.4(FPR1):c.595A>T (p.Thr199Ser)	Gingival disorder [RCV005191509]	uncertain significance	19	51746400	51746400	Human	1	name
597935211	CV3845198	single nucleotide variant	NM_002029.4(FPR1):c.649G>A (p.Val217Ile)	Gingival disorder [RCV005186511]	uncertain significance	19	51746346	51746346	Human	1	name
597878361	CV3860392	single nucleotide variant	NM_002029.4(FPR1):c.677C>T (p.Thr226Ile)	Gingival disorder [RCV005198601]	uncertain significance	19	51746318	51746318	Human	1	name
12896383	CV390318	single nucleotide variant	NM_002029.4(FPR1):c.576T>G (p.Asn192Lys)	Gingival disorder [RCV002230302]\|not provided [RCV001618691]\|not specified [RCV000455271]	benign	19	51746419	51746419	Human	1	name
12896203	CV390432	single nucleotide variant	NM_002029.4(FPR1):c.301G>C (p.Val101Leu)	Gingival disorder [RCV002230084]\|not provided [RCV001824774]\|not specified [RCV000455030]	benign\|not provided	19	51746694	51746694	Human	4	name
12896203	CV390432	single nucleotide variant	NM_002029.4(FPR1):c.301G>C (p.Val101Leu)	Gingival disorder [RCV002230084]\|not provided [RCV001824774]\|not specified [RCV000455030]	benign\|not provided	19	51746694	51746695	Human	4	name
598229973	CV3970073	single nucleotide variant	NM_002029.4(FPR1):c.659G>C (p.Ser220Thr)	not specified [RCV005342164]	uncertain significance	19	51746336	51746336	Human		name
13468662	CV470227	single nucleotide variant	NM_002029.4(FPR1):c.488G>A (p.Arg163His)	FPR1-related disorder [RCV003915486]\|Gingival disorder [RCV002231004]\|not provided [RCV004717651]	benign\|likely benign	19	51746507	51746507	Human	1	name , trait , alternate_id
13613301	CV533359	single nucleotide variant	NM_002029.4(FPR1):c.827A>G (p.Tyr276Cys)	Gingival disorder [RCV002234398]	uncertain significance	19	51746168	51746168	Human	1	name
13613296	CV533361	single nucleotide variant	NM_002029.4(FPR1):c.806G>A (p.Arg269His)	FPR1-related disorder [RCV003905688]\|Gingival disorder [RCV002233923]	benign	19	51746189	51746189	Human	1	name , trait , alternate_id
13613299	CV533439	single nucleotide variant	NM_002029.4(FPR1):c.674C>T (p.Ala225Val)	Gingival disorder [RCV002234399]\|not specified [RCV004025395]	uncertain significance	19	51746321	51746321	Human	1	name
13822605	CV571068	single nucleotide variant	NM_002029.4(FPR1):c.805C>T (p.Arg269Cys)	Gingival disorder [RCV002233642]	uncertain significance	19	51746190	51746190	Human	1	name
13822316	CV572783	single nucleotide variant	NM_002029.4(FPR1):c.409C>T (p.Arg137Cys)	Gingival disorder [RCV002233629]	uncertain significance	19	51746586	51746586	Human	1	name
13807092	CV573400	single nucleotide variant	NM_002029.4(FPR1):c.534T>A (p.Phe178Leu)	Periodontitis [RCV000686521]	uncertain significance	19	51746461	51746461	Human	2	name
14717221	CV648438	single nucleotide variant	NM_002029.4(FPR1):c.710G>A (p.Ser237Asn)	Gingival disorder [RCV002233871]	uncertain significance	19	51746285	51746285	Human	1	name
14711963	CV648439	single nucleotide variant	NM_002029.4(FPR1):c.559C>T (p.Pro187Ser)	Gingival disorder [RCV002233855]\|not specified [RCV004027451]	uncertain significance	19	51746436	51746436	Human	1	name
14731031	CV648440	single nucleotide variant	NM_002029.4(FPR1):c.542C>T (p.Ser181Leu)	Gingival disorder [RCV002235101]	uncertain significance	19	51746453	51746453	Human	1	name
14730545	CV648441	single nucleotide variant	NM_002029.4(FPR1):c.511A>C (p.Thr171Pro)	Gingival disorder [RCV002234904]	uncertain significance	19	51746484	51746484	Human	1	name
14702706	CV648442	single nucleotide variant	NM_002029.4(FPR1):c.439A>G (p.Ile147Val)	Gingival disorder [RCV002235535]	uncertain significance	19	51746556	51746556	Human	1	name
14704829	CV648443	single nucleotide variant	NM_002029.4(FPR1):c.379G>A (p.Val127Ile)	Gingival disorder [RCV002235323]	uncertain significance	19	51746616	51746616	Human	1	name
15136471	CV716655	single nucleotide variant	NM_002029.4(FPR1):c.607A>G (p.Ile203Val)	Gingival disorder [RCV002235844]	likely benign	19	51746388	51746388	Human	1	name
15149612	CV716656	single nucleotide variant	NM_002029.4(FPR1):c.368G>A (p.Arg123His)	FPR1-related disorder [RCV003928434]\|Gingival disorder [RCV002235847]\|not provided [RCV001529734]	likely benign\|uncertain significance	19	51746627	51746627	Human	1	name , trait , alternate_id
26921935	CV848029	single nucleotide variant	NM_002029.4(FPR1):c.955A>C (p.Ser319Arg)	Gingival disorder [RCV002240319]	uncertain significance	19	51746040	51746040	Human	1	name
26918033	CV848030	single nucleotide variant	NM_002029.4(FPR1):c.952G>A (p.Ala318Thr)	Gingival disorder [RCV002239335]	uncertain significance	19	51746043	51746043	Human	1	name
26913567	CV848032	single nucleotide variant	NM_002029.4(FPR1):c.898C>G (p.Leu300Val)	Gingival disorder [RCV002239274]	uncertain significance	19	51746097	51746097	Human	1	name
26888169	CV848033	single nucleotide variant	NM_002029.4(FPR1):c.826T>C (p.Tyr276His)	Gingival disorder [RCV002240341]	uncertain significance	19	51746169	51746169	Human	1	name
26914567	CV848034	single nucleotide variant	NM_002029.4(FPR1):c.736G>T (p.Val246Phe)	Gingival disorder [RCV002237134]	uncertain significance	19	51746259	51746259	Human	1	name
26920222	CV848035	single nucleotide variant	NM_002029.4(FPR1):c.713G>A (p.Arg238His)	Gingival disorder [RCV002240186]	uncertain significance	19	51746282	51746282	Human	1	name
26887318	CV848036	single nucleotide variant	NM_002029.4(FPR1):c.613C>T (p.Arg205Trp)	Gingival disorder [RCV002240265]	uncertain significance	19	51746382	51746382	Human	1	name
26892255	CV848037	single nucleotide variant	NM_002029.4(FPR1):c.570G>C (p.Arg190Ser)	Gingival disorder [RCV002240490]	uncertain significance	19	51746425	51746425	Human	1	name
26918285	CV848038	single nucleotide variant	NM_002029.4(FPR1):c.440T>C (p.Ile147Thr)	Gingival disorder [RCV002239346]\|not provided [RCV003490023]	uncertain significance	19	51746555	51746555	Human	1	name
26898780	CV848039	single nucleotide variant	NM_002029.4(FPR1):c.331G>A (p.Gly111Arg)	Gingival disorder [RCV002240536]	uncertain significance	19	51746664	51746664	Human	1	name
26913220	CV853050	single nucleotide variant	NM_002029.4(FPR1):c.568A>T (p.Arg190Trp)	FPR1 POLYMORPHISM [RCV001035430]\|Gingival disorder [RCV002239272]\|not provided [RCV001655668]	benign	19	51746427	51746427	Human	1	name , trait
38493419	CV929100	single nucleotide variant	NM_002029.4(FPR1):c.823A>G (p.Met275Val)	Gingival disorder [RCV002241311]	uncertain significance	19	51746172	51746172	Human	1	name
38489225	CV929101	single nucleotide variant	NM_002029.4(FPR1):c.722G>A (p.Arg241Gln)	Gingival disorder [RCV002241289]	uncertain significance	19	51746273	51746273	Human	1	name
38492411	CV929102	single nucleotide variant	NM_002029.4(FPR1):c.664G>A (p.Gly222Arg)	Periodontitis [RCV001223564]	uncertain significance	19	51746331	51746331	Human	2	name
38479643	CV929103	single nucleotide variant	NM_002029.4(FPR1):c.596C>T (p.Thr199Met)	Gingival disorder [RCV002241128]	uncertain significance	19	51746399	51746399	Human	1	name
38484947	CV938842	single nucleotide variant	NM_002029.4(FPR1):c.721C>T (p.Arg241Trp)	Gingival disorder [RCV002241058]	uncertain significance	19	51746274	51746274	Human	1	name
38473013	CV950907	single nucleotide variant	NM_002029.4(FPR1):c.943G>A (p.Ala315Thr)	Gingival disorder [RCV002241459]	uncertain significance	19	51746052	51746052	Human	1	name
38479006	CV950908	single nucleotide variant	NM_002029.4(FPR1):c.919G>A (p.Asp307Asn)	Gingival disorder [RCV002241487]	uncertain significance	19	51746076	51746076	Human	1	name
38458327	CV950909	single nucleotide variant	NM_002029.4(FPR1):c.751T>C (p.Phe251Leu)	Gingival disorder [RCV002241585]	uncertain significance	19	51746244	51746244	Human	1	name
38486452	CV950910	single nucleotide variant	NM_002029.4(FPR1):c.634G>A (p.Ala212Thr)	Gingival disorder [RCV002241504]	uncertain significance	19	51746361	51746361	Human	1	name
38493890	CV958727	single nucleotide variant	NM_002029.4(FPR1):c.497C>T (p.Thr166Ile)	Gingival disorder [RCV002563987]	uncertain significance	19	51746498	51746498	Human	1	name
126753925	CV998794	single nucleotide variant	NM_002029.4(FPR1):c.976G>A (p.Glu326Lys)	Gingival disorder [RCV002241875]	uncertain significance	19	51746019	51746019	Human	1	name
151884375	CV1432375	single nucleotide variant	NM_002029.4(FPR1):c.1016C>T (p.Thr339Ile)	Gingival disorder [RCV002000260]	uncertain significance	19	51745979	51745979	Human	1	name
405059645	CV2939403	single nucleotide variant	NM_002029.4(FPR1):c.1010A>G (p.Asn337Ser)	Gingival disorder [RCV003762276]	uncertain significance	19	51745985	51745985	Human	1	name
405064204	CV3000802	single nucleotide variant	NM_002029.4(FPR1):c.1015A>G (p.Thr339Ala)	Gingival disorder [RCV003762666]	uncertain significance	19	51745980	51745980	Human	1	name
12896988	CV390308	single nucleotide variant	NM_002029.4(FPR1):c.1037A>C (p.Glu346Ala)	Gingival disorder [RCV002230300]\|not provided [RCV001824772]\|not specified [RCV000456087]	benign\|not provided	19	51745958	51745958	Human	1	name
597952987	CV3775856	deletion	NM_002029.4(FPR1):c.540_541del (p.Ser181fs)	Gingival disorder [RCV005121399]	uncertain significance	19	51746454	51746455	Human	1	name
155950462	CV2084386	deletion	NM_002029.4(FPR1):c.396del (p.Val131_Trp132insTer)	Gingival disorder [RCV002880471]	uncertain significance	19	51746599	51746599	Human	1	name
13613230	CV533358	indel	NM_002029.4(FPR1):c.1037_1038delinsCA (p.Glu346Ala)	Gingival disorder [RCV002528851]	benign	19	51745957	51745958	Human		name
597968944	CV3791161	duplication	NM_002029.4(FPR1):c.557_723dup (p.Val242delinsThrLeuLysArgGlyTer)	Gingival disorder [RCV005141193]	uncertain significance	19	51746271	51746272	Human	1	name

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