ClinVar for Gene (Select 115352) - ClinVar

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Links from Gene

Items: 74

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3278395	NM_052939.4(FCRL3):c.1102C>T (p.Leu368Phe)	FCRL3 (L368F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3278394	NM_052939.4(FCRL3):c.1108A>G (p.Thr370Ala)	FCRL3 (T370A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3278393	NM_052939.4(FCRL3):c.926G>T (p.Cys309Phe)	FCRL3 (C309F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3278392	NM_052939.4(FCRL3):c.1298G>A (p.Gly433Glu)	FCRL3 (G433E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3278390	NM_052939.4(FCRL3):c.73C>T (p.Leu25Phe)	FCRL3 (L25F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3278389	NM_052939.4(FCRL3):c.125T>C (p.Leu42Pro)	FCRL3 (L42P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3278388	NM_052939.4(FCRL3):c.328G>T (p.Val110Phe)	FCRL3 (V110F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3242278	GRCh37/hg19 1q22-23.2(chr1:155709113-159191078)x3	ACKR1, AIM2 +80 more	Copy number gain	not provided	GLikely pathogenic
Select item 3094206	NM_052939.4(FCRL3):c.94T>A (p.Ser32Thr)	FCRL3 (S32T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3094205	NM_052939.4(FCRL3):c.834A>G (p.Ile278Met)	FCRL3 (I278M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3094204	NM_052939.4(FCRL3):c.791C>G (p.Thr264Arg)	FCRL3 (T264R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3094203	NM_052939.4(FCRL3):c.722G>A (p.Arg241Lys)	FCRL3 (R241K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3094201	NM_052939.4(FCRL3):c.548T>C (p.Ile183Thr)	FCRL3 (I183T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3094200	NM_052939.4(FCRL3):c.47A>G (p.Gln16Arg)	FCRL3 (Q16R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3094198	NM_052939.4(FCRL3):c.2104G>A (p.Asp702Asn)	FCRL3 (D702N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3094197	NM_052939.4(FCRL3):c.2021A>G (p.Asn674Ser)	FCRL3 (N674S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3094196	NM_052939.4(FCRL3):c.1756G>A (p.Val586Ile)	FCRL3 (V586I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3094195	NM_052939.4(FCRL3):c.1720G>T (p.Ala574Ser)	FCRL3 (A574S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3094194	NM_052939.4(FCRL3):c.1720G>A (p.Ala574Thr)	FCRL3 (A574T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3094193	NM_052939.4(FCRL3):c.1580G>A (p.Gly527Glu)	FCRL3 (G527E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3094192	NM_052939.4(FCRL3):c.1484T>C (p.Leu495Pro)	FCRL3 (L495P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3094191	NM_052939.4(FCRL3):c.1450G>A (p.Gly484Arg)	FCRL3 (G484R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3094190	NM_052939.4(FCRL3):c.1382A>G (p.His461Arg)	FCRL3 (H461R)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3094189	NM_052939.4(FCRL3):c.1328C>T (p.Ala443Val)	FCRL3 (A443V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3062988	GRCh37/hg19 1q21.1-23.1(chr1:144368497-158992086)x3	ACP6, ADAM15 +315 more	Copy number gain	not specified	GPathogenic
Select item 3024728	NM_052939.4(FCRL3):c.935C>A (p.Ala312Asp)	FCRL3 (A312D)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2681280	NM_052939.4(FCRL3):c.1087G>A (p.Val363Ile)	FCRL3 (V363I)	Single nucleotide variant (missense variant +1 more)	EBV-positive nodal T- and NK-cell lymphoma	GLikely benign
Select item 2615762	NM_052939.4(FCRL3):c.599C>A (p.Thr200Lys)	FCRL3 (T200K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2605372	NM_052939.4(FCRL3):c.1514C>T (p.Pro505Leu)	FCRL3 (P505L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2598010	NM_052939.4(FCRL3):c.1676C>T (p.Thr559Ile)	FCRL3 (T559I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2597492	NM_052939.4(FCRL3):c.915G>C (p.Met305Ile)	FCRL3 (M305I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2580317	GRCh37/hg19 1q12-23.1(chr1:142535935-157648813)x3	ACP6, ADAM15 +293 more	Copy number gain	Chromosome 1q21.1 duplication syndrome	GPathogenic
Select item 2547589	NM_052939.4(FCRL3):c.1871C>T (p.Ser624Leu)	FCRL3 (S624L)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2539505	NM_052939.4(FCRL3):c.2075A>G (p.Tyr692Cys)	FCRL3 (Y692C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2528811	NM_052939.4(FCRL3):c.1679T>C (p.Leu560Pro)	FCRL3 (L560P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2528300	NM_052939.4(FCRL3):c.1417G>A (p.Val473Met)	FCRL3 (V473M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2526061	NM_052939.4(FCRL3):c.1363A>G (p.Asn455Asp)	FCRL3 (N455D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2521728	NM_052939.4(FCRL3):c.209A>G (p.Asp70Gly)	FCRL3 (D70G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2478921	NM_052939.4(FCRL3):c.599C>T (p.Thr200Met)	FCRL3 (T200M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2461241	NM_052939.4(FCRL3):c.53G>T (p.Gly18Val)	FCRL3 (G18V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2457363	NM_052939.4(FCRL3):c.1930A>G (p.Met644Val)	FCRL3 (M644V)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2396096	NM_052939.4(FCRL3):c.584G>A (p.Arg195Lys)	FCRL3 (R195K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2393638	NM_052939.4(FCRL3):c.1799G>A (p.Arg600Gln)	FCRL3 (R600Q)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2393637	NM_052939.4(FCRL3):c.1537G>A (p.Glu513Lys)	FCRL3 (E513K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2393190	NM_052939.4(FCRL3):c.1956T>A (p.Asn652Lys)	FCRL3 (N652K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2391651	NM_052939.4(FCRL3):c.437T>C (p.Leu146Ser)	FCRL3 (L146S)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2390764	NM_052939.4(FCRL3):c.158A>G (p.Gln53Arg)	FCRL3 (Q53R)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2386638	NM_052939.4(FCRL3):c.1507T>G (p.Ser503Ala)	FCRL3 (S503A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2358533	NM_052939.4(FCRL3):c.836G>A (p.Arg279His)	FCRL3 (R279H)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2350282	NM_052939.4(FCRL3):c.1811G>A (p.Gly604Glu)	FCRL3 (G604E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2345494	NM_052939.4(FCRL3):c.1031A>T (p.His344Leu)	FCRL3 (H344L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2342047	NM_052939.4(FCRL3):c.315G>C (p.Gln105His)	FCRL3 (Q105H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2319136	NM_052939.4(FCRL3):c.446T>A (p.Ile149Asn)	FCRL3 (I149N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2302529	NM_052939.4(FCRL3):c.118G>C (p.Val40Leu)	FCRL3 (V40L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2288157	NM_052939.4(FCRL3):c.958T>C (p.Phe320Leu)	FCRL3 (F320L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2284864	NM_052939.4(FCRL3):c.617C>T (p.Pro206Leu)	FCRL3 (P206L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2255280	NM_052939.4(FCRL3):c.762C>A (p.Asp254Glu)	FCRL3 (D254E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2250180	NM_052939.4(FCRL3):c.992T>C (p.Leu331Pro)	FCRL3 (L331P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2249059	NM_052939.4(FCRL3):c.394G>A (p.Val132Ile)	FCRL3 (V132I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2225612	NM_052939.4(FCRL3):c.1120G>A (p.Val374Ile)	FCRL3 (V374I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2218536	NM_052939.4(FCRL3):c.1966G>A (p.Gly656Arg)	FCRL3 (G656R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2210700	NM_052939.4(FCRL3):c.4C>G (p.Leu2Val)	FCRL3 (L2V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1291670	NM_052939.4(FCRL3):c.2162A>G (p.Asn721Ser)	FCRL3 (N721S)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 1003645	NC_000001.10:g.(?_130980840)_(248900000_?)dup	FCGR3A, LCE3C +956 more	Duplication	Parathyroid carcinoma +2 more	GUncertain significance
Select item 776340	NM_052939.4(FCRL3):c.1132A>G (p.Ile378Val)	FCRL3 (I378V)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 775145	NM_052939.4(FCRL3):c.878G>T (p.Arg293Leu)	FCRL3 (R293L)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 731957	NM_052939.4(FCRL3):c.919C>T (p.Leu307Phe)	FCRL3 (L307F)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 716374	NM_052939.4(FCRL3):c.1854G>A (p.Glu618=)	FCRL3	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 688082	GRCh37/hg19 1q23.1-24.2(chr1:157321299-167391423)x1	ACKR1, ADAMTS4 +132 more	Copy number loss	not provided	GPathogenic
Select item 565186	GRCh37/hg19 1q23.1(chr1:157347489-157804172)x3	FCRL1, FCRL5 +4 more	Copy number gain	not provided	GUncertain significance
Select item 565183	GRCh37/hg19 1q22-23.1(chr1:155636337-158024499)x1	ARHGEF11, ARHGEF2 +57 more	Copy number loss	not provided	GPathogenic
Select item 442387	GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)	CD34, CD46 +2014 more	Copy number gain	See cases	GPathogenic
Select item 442386	GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3	GPATCH2, GPATCH3 +2014 more	Copy number gain	See cases	GPathogenic
Select item 155448	GRCh38/hg38 1q21.2-25.2(chr1:149854269-180267197)x3	LOC129931453, LOC129931454 +1585 more	Copy number gain	See cases	GPathogenic

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Links from Gene

Items: 74