ClinVar for Gene (Select 157285) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3309653	NM_001080826.3(PRAG1):c.2497T>G (p.Trp833Gly)	PRAG1 (W833G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309652	NM_001080826.3(PRAG1):c.3853G>A (p.Glu1285Lys)	PRAG1 (E1285K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309651	NM_001080826.3(PRAG1):c.3521C>T (p.Pro1174Leu)	PRAG1 (P1174L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309649	NM_001080826.3(PRAG1):c.2359G>A (p.Gly787Arg)	PRAG1 (G787R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309648	NM_001080826.3(PRAG1):c.2468G>A (p.Arg823Gln)	PRAG1 (R823Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309647	NM_001080826.3(PRAG1):c.3517G>A (p.Ala1173Thr)	PRAG1 (A1173T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309646	NM_001080826.3(PRAG1):c.410G>A (p.Arg137Gln)	PRAG1 (R137Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309645	NM_001080826.3(PRAG1):c.3532G>T (p.Ala1178Ser)	PRAG1 (A1178S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309644	NM_001080826.3(PRAG1):c.3556C>T (p.Pro1186Ser)	PRAG1 (P1186S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309643	NM_001080826.3(PRAG1):c.1174G>T (p.Gly392Trp)	PRAG1 (G392W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309642	NM_001080826.3(PRAG1):c.1991A>G (p.Asp664Gly)	PRAG1 (D664G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309641	NM_001080826.3(PRAG1):c.2698G>T (p.Gly900Cys)	PRAG1 (G900C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309640	NM_001080826.3(PRAG1):c.4211A>G (p.Gln1404Arg)	PRAG1 (Q1404R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309638	NM_001080826.3(PRAG1):c.3302C>G (p.Ser1101Cys)	PRAG1 (S1101C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309637	NM_001080826.3(PRAG1):c.2537A>G (p.Lys846Arg)	PRAG1 (K846R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309636	NM_001080826.3(PRAG1):c.1633C>T (p.Pro545Ser)	PRAG1 (P545S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309635	NM_001080826.3(PRAG1):c.2525C>G (p.Thr842Arg)	PRAG1 (T842R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309634	NM_001080826.3(PRAG1):c.967C>G (p.Leu323Val)	PRAG1 (L323V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309633	NM_001080826.3(PRAG1):c.2345C>T (p.Ser782Leu)	PRAG1 (S782L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309632	NM_001080826.3(PRAG1):c.3008C>T (p.Ser1003Leu)	PRAG1 (S1003L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309631	NM_001080826.3(PRAG1):c.2720G>T (p.Ser907Ile)	PRAG1 (S907I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309630	NM_001080826.3(PRAG1):c.623G>A (p.Arg208His)	PRAG1 (R208H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309629	NM_001080826.3(PRAG1):c.1639A>G (p.Lys547Glu)	PRAG1 (K547E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309627	NM_001080826.3(PRAG1):c.2507G>C (p.Gly836Ala)	PRAG1 (G836A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309626	NM_001080826.3(PRAG1):c.2018G>A (p.Arg673His)	PRAG1 (R673H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309625	NM_001080826.3(PRAG1):c.3550G>A (p.Ala1184Thr)	PRAG1 (A1184T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309624	NM_001080826.3(PRAG1):c.2583C>A (p.His861Gln)	PRAG1 (H861Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309623	NM_001080826.3(PRAG1):c.1456C>T (p.Arg486Trp)	PRAG1 (R486W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218110	NM_001080826.3(PRAG1):c.962C>T (p.Ser321Phe)	PRAG1 (S321F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218109	NM_001080826.3(PRAG1):c.961T>C (p.Ser321Pro)	PRAG1 (S321P)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3218108	NM_001080826.3(PRAG1):c.926A>C (p.Lys309Thr)	PRAG1 (K309T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218107	NM_001080826.3(PRAG1):c.914C>G (p.Pro305Arg)	PRAG1 (P305R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218106	NM_001080826.3(PRAG1):c.908G>A (p.Arg303Gln)	PRAG1 (R303Q)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3218105	NM_001080826.3(PRAG1):c.892G>A (p.Ala298Thr)	PRAG1 (A298T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3218104	NM_001080826.3(PRAG1):c.860C>T (p.Thr287Met)	PRAG1 (T287M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218103	NM_001080826.3(PRAG1):c.785G>T (p.Gly262Val)	PRAG1 (G262V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218102	NM_001080826.3(PRAG1):c.745G>C (p.Glu249Gln)	PRAG1 (E249Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218101	NM_001080826.3(PRAG1):c.697C>A (p.Pro233Thr)	PRAG1 (P233T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218100	NM_001080826.3(PRAG1):c.679C>T (p.Pro227Ser)	PRAG1 (P227S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218099	NM_001080826.3(PRAG1):c.679C>G (p.Pro227Ala)	PRAG1 (P227A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218098	NM_001080826.3(PRAG1):c.599G>A (p.Arg200Gln)	PRAG1 (R200Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218097	NM_001080826.3(PRAG1):c.598C>T (p.Arg200Trp)	PRAG1 (R200W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218096	NM_001080826.3(PRAG1):c.577C>T (p.Pro193Ser)	PRAG1 (P193S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218095	NM_001080826.3(PRAG1):c.551A>G (p.Glu184Gly)	PRAG1 (E184G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218094	NM_001080826.3(PRAG1):c.509G>A (p.Arg170His)	PRAG1 (R170H)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3218093	NM_001080826.3(PRAG1):c.508C>T (p.Arg170Cys)	PRAG1 (R170C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218091	NM_001080826.3(PRAG1):c.476A>G (p.Tyr159Cys)	PRAG1 (Y159C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218090	NM_001080826.3(PRAG1):c.4204C>G (p.Leu1402Val)	PRAG1 (L1402V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218089	NM_001080826.3(PRAG1):c.4180G>A (p.Gly1394Arg)	PRAG1 (G1394R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218088	NM_001080826.3(PRAG1):c.4019C>T (p.Pro1340Leu)	PRAG1 (P1340L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218087	NM_001080826.3(PRAG1):c.3954C>G (p.Ile1318Met)	PRAG1 (I1318M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218086	NM_001080826.3(PRAG1):c.3833G>A (p.Arg1278Gln)	PRAG1 (R1278Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218085	NM_001080826.3(PRAG1):c.379G>T (p.Asp127Tyr)	PRAG1 (D127Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218084	NM_001080826.3(PRAG1):c.3807C>G (p.Asn1269Lys)	PRAG1 (N1269K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218083	NM_001080826.3(PRAG1):c.3620A>G (p.Lys1207Arg)	PRAG1 (K1207R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218082	NM_001080826.3(PRAG1):c.3569G>A (p.Gly1190Asp)	PRAG1 (G1190D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218081	NM_001080826.3(PRAG1):c.3527C>T (p.Ala1176Val)	PRAG1 (A1176V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218080	NM_001080826.3(PRAG1):c.3506C>A (p.Ala1169Asp)	PRAG1 (A1169D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218079	NM_001080826.3(PRAG1):c.3449A>G (p.Asn1150Ser)	PRAG1 (N1150S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218078	NM_001080826.3(PRAG1):c.341G>A (p.Arg114Lys)	PRAG1 (R114K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218077	NM_001080826.3(PRAG1):c.3419G>A (p.Gly1140Glu)	PRAG1 (G1140E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218076	NM_001080826.3(PRAG1):c.3402G>T (p.Glu1134Asp)	PRAG1 (E1134D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218075	NM_001080826.3(PRAG1):c.3338C>A (p.Ala1113Glu)	PRAG1 (A1113E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218074	NM_001080826.3(PRAG1):c.3313C>T (p.Arg1105Trp)	PRAG1 (R1105W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218073	NM_001080826.3(PRAG1):c.3241C>T (p.Pro1081Ser)	PRAG1 (P1081S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218072	NM_001080826.3(PRAG1):c.3238C>A (p.Pro1080Thr)	PRAG1 (P1080T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218071	NM_001080826.3(PRAG1):c.3218T>A (p.Val1073Glu)	PRAG1 (V1073E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218070	NM_001080826.3(PRAG1):c.3199G>A (p.Asp1067Asn)	PRAG1 (D1067N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218069	NM_001080826.3(PRAG1):c.317C>T (p.Ala106Val)	PRAG1 (A106V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218068	NM_001080826.3(PRAG1):c.3159C>G (p.His1053Gln)	PRAG1 (H1053Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218067	NM_001080826.3(PRAG1):c.3113G>A (p.Ser1038Asn)	PRAG1 (S1038N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218066	NM_001080826.3(PRAG1):c.3062A>G (p.Tyr1021Cys)	PRAG1 (Y1021C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218065	NM_001080826.3(PRAG1):c.3019A>G (p.Ile1007Val)	PRAG1 (I1007V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218064	NM_001080826.3(PRAG1):c.3011G>T (p.Gly1004Val)	PRAG1 (G1004V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218063	NM_001080826.3(PRAG1):c.2967G>T (p.Trp989Cys)	PRAG1 (W989C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218062	NM_001080826.3(PRAG1):c.293T>G (p.Val98Gly)	PRAG1 (V98G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218061	NM_001080826.3(PRAG1):c.2756C>T (p.Ser919Leu)	PRAG1 (S919L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218060	NM_001080826.3(PRAG1):c.2732A>T (p.Gln911Leu)	PRAG1 (Q911L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218059	NM_001080826.3(PRAG1):c.2716G>C (p.Gly906Arg)	PRAG1 (G906R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218058	NM_001080826.3(PRAG1):c.2669G>A (p.Gly890Asp)	PRAG1 (G890D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218057	NM_001080826.3(PRAG1):c.2638G>C (p.Asp880His)	PRAG1 (D880H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218056	NM_001080826.3(PRAG1):c.2617C>T (p.His873Tyr)	PRAG1 (H873Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218055	NM_001080826.3(PRAG1):c.2605G>A (p.Gly869Arg)	PRAG1 (G869R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218054	NM_001080826.3(PRAG1):c.2597T>C (p.Leu866Ser)	PRAG1 (L866S)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3218053	NM_001080826.3(PRAG1):c.2594C>T (p.Ser865Leu)	PRAG1 (S865L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218052	NM_001080826.3(PRAG1):c.2534C>T (p.Pro845Leu)	PRAG1 (P845L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218051	NM_001080826.3(PRAG1):c.250A>G (p.Ile84Val)	PRAG1 (I84V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218050	NM_001080826.3(PRAG1):c.2414C>A (p.Ser805Tyr)	PRAG1 (S805Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218049	NM_001080826.3(PRAG1):c.2384C>T (p.Pro795Leu)	PRAG1 (P795L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218048	NM_001080826.3(PRAG1):c.2375C>A (p.Ala792Asp)	PRAG1 (A792D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218047	NM_001080826.3(PRAG1):c.2324C>A (p.Pro775His)	PRAG1 (P775H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218046	NM_001080826.3(PRAG1):c.2314G>A (p.Asp772Asn)	PRAG1 (D772N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218045	NM_001080826.3(PRAG1):c.2210G>A (p.Ser737Asn)	PRAG1 (S737N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218044	NM_001080826.3(PRAG1):c.218G>A (p.Gly73Asp)	PRAG1 (G73D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218043	NM_001080826.3(PRAG1):c.2181C>G (p.Asn727Lys)	PRAG1 (N727K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218042	NM_001080826.3(PRAG1):c.2167C>T (p.Leu723Phe)	PRAG1 (L723F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218041	NM_001080826.3(PRAG1):c.2163G>A (p.Arg721=)	PRAG1	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 3218039	NM_001080826.3(PRAG1):c.2135C>T (p.Ser712Leu)	PRAG1 (S712L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218038	NM_001080826.3(PRAG1):c.2113A>G (p.Arg705Gly)	PRAG1 (R705G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218037	NM_001080826.3(PRAG1):c.2044G>T (p.Gly682Trp)	PRAG1 (G682W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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