ClinVar for Gene (Select 2357) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3040106	NM_002029.4(FPR1):c.1038G>A (p.Glu346=)	FPR1	Single nucleotide variant (synonymous variant)	FPR1-related disorder	GLikely benign
Select item 3023284	NM_002029.4(FPR1):c.350C>T (p.Ala117Val)	FPR1 (A117V)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 3017822	NM_002029.4(FPR1):c.554A>G (p.Asn185Ser)	FPR1 (N185S)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 3017810	NM_002029.4(FPR1):c.436A>G (p.Ile146Val)	FPR1 (I146V)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 3015092	NM_002029.4(FPR1):c.346A>T (p.Ile116Phe)	FPR1 (I116F)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 3007275	NM_002029.4(FPR1):c.405C>T (p.Asn135=)	FPR1	Single nucleotide variant (synonymous variant)	Gingival disorder	GLikely benign
Select item 2994071	NM_002029.4(FPR1):c.77A>G (p.Asp26Gly)	FPR1 (D26G)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 2988746	NM_002029.4(FPR1):c.897G>A (p.Met299Ile)	FPR1 (M299I)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 2988146	NM_002029.4(FPR1):c.139G>A (p.Val47Met)	FPR1 (V47M)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 2983753	NM_002029.4(FPR1):c.548G>A (p.Trp183Ter)	FPR1 (W183*)	Single nucleotide variant (nonsense)	Gingival disorder	GUncertain significance
Select item 2914038	NM_002029.4(FPR1):c.524C>T (p.Ala175Val)	FPR1 (A175V)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 2912940	NM_002029.4(FPR1):c.853G>A (p.Val285Met)	FPR1 (V285M)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 2893989	NM_002029.4(FPR1):c.333A>G (p.Gly111=)	FPR1	Single nucleotide variant (synonymous variant)	Gingival disorder	GLikely benign
Select item 2886675	NM_002029.4(FPR1):c.841A>G (p.Ile281Val)	FPR1 (I281V)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 2879585	NM_002029.4(FPR1):c.244A>G (p.Met82Val)	FPR1 (M82V)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 2877381	NM_002029.4(FPR1):c.484A>G (p.Ile162Val)	FPR1 (I162V)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 2876451	NM_002029.4(FPR1):c.918G>A (p.Gln306=)	FPR1	Single nucleotide variant (synonymous variant)	Gingival disorder	GLikely benign
Select item 2872194	NM_002029.4(FPR1):c.410G>A (p.Arg137His)	FPR1 (R137H)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 2868959	NM_002029.4(FPR1):c.443G>C (p.Gly148Ala)	FPR1 (G148A)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 2859305	NM_002029.4(FPR1):c.829A>C (p.Lys277Gln)	FPR1 (K277Q)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 2842265	NM_002029.4(FPR1):c.1015A>G (p.Thr339Ala)	FPR1 (T339A)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 2841372	NM_002029.4(FPR1):c.15C>T (p.Ser5=)	FPR1	Single nucleotide variant (synonymous variant)	Gingival disorder	GLikely benign
Select item 2820782	NM_002029.4(FPR1):c.642G>A (p.Met214Ile)	FPR1 (M214I)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 2815720	NM_002029.4(FPR1):c.641T>G (p.Met214Arg)	FPR1 (M214R)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 2798963	NM_002029.4(FPR1):c.624T>C (p.Ile208=)	FPR1	Single nucleotide variant (synonymous variant)	Gingival disorder	GLikely benign
Select item 2796126	NM_002029.4(FPR1):c.56C>G (p.Ser19Cys)	FPR1 (S19C)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 2788195	NM_002029.4(FPR1):c.1010A>G (p.Asn337Ser)	FPR1 (N337S)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 2787793	NM_002029.4(FPR1):c.44C>A (p.Thr15Lys)	FPR1 (T15K)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 2754690	NM_002029.4(FPR1):c.77A>C (p.Asp26Ala)	FPR1 (D26A)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 2751758	NM_002029.4(FPR1):c.258C>T (p.Ala86=)	FPR1	Single nucleotide variant (synonymous variant)	Gingival disorder	GLikely benign
Select item 2751433	NM_002029.4(FPR1):c.144C>T (p.Ile48=)	FPR1	Single nucleotide variant (synonymous variant)	Gingival disorder	GLikely benign
Select item 2729628	NM_002029.4(FPR1):c.352C>G (p.Leu118Val)	FPR1 (L118V)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 2726296	NM_002029.4(FPR1):c.444G>T (p.Gly148=)	FPR1	Single nucleotide variant (synonymous variant)	Gingival disorder	GLikely benign
Select item 2717624	NM_002029.4(FPR1):c.739G>A (p.Ala247Thr)	FPR1 (A247T)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 2714964	NM_002029.4(FPR1):c.17C>T (p.Ser6Phe)	FPR1 (S6F)	Single nucleotide variant (missense variant)	Gingival disorder	GLikely benign
Select item 2714023	NM_002029.4(FPR1):c.69C>T (p.Leu23=)	FPR1	Single nucleotide variant (synonymous variant)	Gingival disorder	GLikely benign
Select item 2712434	NM_002029.4(FPR1):c.208G>A (p.Ala70Thr)	FPR1 (A70T)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 2684892	GRCh37/hg19 19q13.33-13.43(chr19:49625130-57647352)x3	ACP4, ADM5 +261 more	Copy number gain	not provided	GLikely pathogenic
Select item 2535491	NM_002029.4(FPR1):c.622A>T (p.Ile208Phe)	FPR1 (I208F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527400	NM_002029.4(FPR1):c.380T>C (p.Val127Ala)	FPR1 (V127A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2501727	NM_002029.4(FPR1):c.443G>A (p.Gly148Glu)	FPR1 (G148E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2421489	NM_002029.4(FPR1):c.465C>T (p.Leu155=)	FPR1	Single nucleotide variant (synonymous variant)	Gingival disorder	GLikely benign
Select item 2419436	NM_002029.4(FPR1):c.682A>T (p.Ile228Phe)	FPR1 (I228F)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 2418855	NM_002029.4(FPR1):c.133G>A (p.Gly45Arg)	FPR1 (G45R)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 2290811	NM_002029.4(FPR1):c.470C>T (p.Thr157Ile)	FPR1 (T157I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248901	NM_002029.4(FPR1):c.283T>G (p.Trp95Gly)	FPR1 (W95G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243854	NM_002029.4(FPR1):c.902A>G (p.Tyr301Cys)	FPR1 (Y301C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2192186	NM_002029.4(FPR1):c.506G>A (p.Gly169Asp)	FPR1 (G169D)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 2189596	NM_002029.4(FPR1):c.284G>T (p.Trp95Leu)	FPR1 (W95L)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 2176439	NM_002029.4(FPR1):c.591G>A (p.Met197Ile)	FPR1 (M197I)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2172572	NM_002029.4(FPR1):c.349G>A (p.Ala117Thr)	FPR1 (A117T)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 2166249	NM_002029.4(FPR1):c.914G>T (p.Gly305Val)	FPR1 (G305V)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 2165787	NM_002029.4(FPR1):c.185T>A (p.Ile62Asn)	FPR1 (I62N)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 2160459	NM_002029.4(FPR1):c.408C>T (p.His136=)	FPR1	Single nucleotide variant (synonymous variant)	Gingival disorder	GLikely benign
Select item 2153999	NM_002029.4(FPR1):c.268C>T (p.His90Tyr)	FPR1 (H90Y)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 2147975	NM_002029.4(FPR1):c.982T>C (p.Ser328Pro)	FPR1 (S328P)	Single nucleotide variant (missense variant)	Gingival disorder +1 more	GUncertain significance
Select item 2102104	NM_002029.4(FPR1):c.1008C>T (p.Thr336=)	FPR1	Single nucleotide variant (synonymous variant)	Gingival disorder	GLikely benign
Select item 2084740	NM_002029.4(FPR1):c.583G>A (p.Val195Ile)	FPR1 (V195I)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 2081908	NM_002029.4(FPR1):c.541T>C (p.Ser181Pro)	FPR1 (S181P)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 2079789	NM_002029.4(FPR1):c.696C>G (p.Gly232=)	FPR1	Single nucleotide variant (synonymous variant)	Gingival disorder	GLikely benign
Select item 2073976	NM_002029.4(FPR1):c.1008C>A (p.Thr336=)	FPR1	Single nucleotide variant (synonymous variant)	Gingival disorder	GLikely benign
Select item 2067291	NM_002029.4(FPR1):c.646A>G (p.Ile216Val)	FPR1 (I216V)	Single nucleotide variant (missense variant)	Gingival disorder +1 more	GUncertain significance
Select item 2066974	NM_002029.4(FPR1):c.726C>A (p.Val242=)	FPR1	Single nucleotide variant (synonymous variant)	Gingival disorder	GLikely benign
Select item 2062740	NM_002029.4(FPR1):c.415G>A (p.Val139Met)	FPR1 (V139M)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 2061092	NM_002029.4(FPR1):c.279C>T (p.Phe93=)	FPR1	Single nucleotide variant (synonymous variant)	Gingival disorder	GLikely benign
Select item 2060598	NM_002029.4(FPR1):c.245T>C (p.Met82Thr)	FPR1 (M82T)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 2042999	NM_002029.4(FPR1):c.52G>A (p.Val18Ile)	FPR1 (V18I)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 2027685	NM_002029.4(FPR1):c.876C>T (p.Phe292=)	FPR1	Single nucleotide variant (synonymous variant)	Gingival disorder	GLikely benign
Select item 2025183	NM_002029.4(FPR1):c.396del (p.Val131_Trp132insTer)	FPR1	Deletion (nonsense)	Gingival disorder	GUncertain significance
Select item 2017348	NM_002029.4(FPR1):c.960G>A (p.Leu320=)	FPR1	Single nucleotide variant (synonymous variant)	Gingival disorder	GLikely benign
Select item 2003590	NM_002029.4(FPR1):c.752T>A (p.Phe251Tyr)	FPR1 (F251Y)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 2002782	NM_002029.4(FPR1):c.211dup (p.Asp71fs)	FPR1 (D71fs)	Duplication (frameshift variant)	Gingival disorder	GUncertain significance
Select item 1986440	NM_002029.4(FPR1):c.648C>T (p.Ile216=)	FPR1	Single nucleotide variant (synonymous variant)	Gingival disorder	GLikely benign
Select item 1986345	NM_002029.4(FPR1):c.118G>A (p.Gly40Arg)	FPR1 (G40R)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 1982065	NM_002029.4(FPR1):c.775G>A (p.Val259Met)	FPR1 (V259M)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 1978514	NM_002029.4(FPR1):c.723G>T (p.Arg241=)	FPR1	Single nucleotide variant (synonymous variant)	Gingival disorder	GLikely benign
Select item 1720614	NM_002029.4(FPR1):c.144C>G (p.Ile48Met)	FPR1 (I48M)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 1719064	NM_002029.4(FPR1):c.589A>G (p.Met197Val)	FPR1 (M197V)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 1653706	NM_002029.4(FPR1):c.486T>C (p.Ile162=)	FPR1	Single nucleotide variant (synonymous variant)	Gingival disorder	GLikely benign
Select item 1650694	NM_002029.4(FPR1):c.414C>T (p.Thr138=)	FPR1	Single nucleotide variant (synonymous variant)	Gingival disorder	GLikely benign
Select item 1643172	NM_002029.4(FPR1):c.132C>T (p.Asn44=)	FPR1	Single nucleotide variant (synonymous variant)	Gingival disorder	GLikely benign
Select item 1614672	NM_002029.4(FPR1):c.975C>G (p.Thr325=)	FPR1	Single nucleotide variant (synonymous variant)	Gingival disorder	GLikely benign
Select item 1592063	NM_002029.4(FPR1):c.339C>A (p.Val113=)	FPR1	Single nucleotide variant (synonymous variant)	Gingival disorder	GLikely benign
Select item 1591420	NM_002029.4(FPR1):c.156A>T (p.Gly52=)	FPR1	Single nucleotide variant (synonymous variant)	Gingival disorder	GLikely benign
Select item 1584479	NM_002029.4(FPR1):c.528C>T (p.Cys176=)	FPR1	Single nucleotide variant (synonymous variant)	Gingival disorder	GLikely benign
Select item 1582623	NM_002029.4(FPR1):c.555C>T (p.Asn185=)	FPR1	Single nucleotide variant (synonymous variant)	Gingival disorder	GLikely benign
Select item 1563303	NM_002029.4(FPR1):c.543G>A (p.Ser181=)	FPR1	Single nucleotide variant (synonymous variant)	Gingival disorder	GLikely benign
Select item 1555380	NM_002029.4(FPR1):c.519A>T (p.Thr173=)	FPR1	Single nucleotide variant (synonymous variant)	Gingival disorder	GLikely benign
Select item 1543507	NM_002029.4(FPR1):c.12T>C (p.Asn4=)	FPR1	Single nucleotide variant (synonymous variant)	Gingival disorder	GLikely benign
Select item 1536699	NM_002029.4(FPR1):c.447C>T (p.Pro149=)	FPR1	Single nucleotide variant (synonymous variant)	Gingival disorder	GLikely benign
Select item 1526670	GRCh37/hg19 19q13.33-13.41(chr19:49911081-53127438)	FPR3, ZNF577 +115 more	Copy number gain	not specified	GLikely pathogenic
Select item 1523521	NM_002029.4(FPR1):c.301G>A (p.Val101Ile)	FPR1 (V101I)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 1515599	NM_002029.4(FPR1):c.257C>T (p.Ala86Val)	FPR1 (A86V)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 1511796	NC_000019.9:g.(?_52249195)_(52250247_?)dup	FPR1	Duplication	Gingival disorder	GUncertain significance
Select item 1502924	NM_002029.4(FPR1):c.487C>T (p.Arg163Cys)	FPR1 (R163C)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 1501594	NM_002029.4(FPR1):c.758G>T (p.Cys253Phe)	FPR1 (C253F)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 1493466	NM_002029.4(FPR1):c.272G>A (p.Trp91Ter)	FPR1 (W91*)	Single nucleotide variant (nonsense)	Gingival disorder	GUncertain significance
Select item 1480296	NM_002029.4(FPR1):c.1016C>T (p.Thr339Ile)	FPR1 (T339I)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 1476955	NM_002029.4(FPR1):c.851A>G (p.Asp284Gly)	FPR1 (D284G)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance
Select item 1449872	NM_002029.4(FPR1):c.652G>T (p.Ala218Ser)	FPR1 (A218S)	Single nucleotide variant (missense variant)	Gingival disorder	GUncertain significance

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