"Ambry Genetics"[submitter] AND "NLRC5"[gene] - ClinVar

Search results

Items: 97

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2255391	NM_001384950.1(NLRC5):c.14G>T (p.Gly5Val)	NLRC5 (G5V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2293505	NM_001384950.1(NLRC5):c.68A>C (p.Lys23Thr)	NLRC5 (K23T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2222026	NM_001384950.1(NLRC5):c.88G>A (p.Ala30Thr)	NLRC5 (A30T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200491	NM_001384950.1(NLRC5):c.116C>T (p.Thr39Met)	NLRC5 (T39M)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2283585	NM_001384950.1(NLRC5):c.126T>G (p.Asp42Glu)	NLRC5 (D42E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2371903	NM_001384950.1(NLRC5):c.136G>A (p.Glu46Lys)	NLRC5 (E46K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2211671	NM_001384950.1(NLRC5):c.155A>G (p.Gln52Arg)	NLRC5 (Q52R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2298258	NM_001384950.1(NLRC5):c.278C>G (p.Thr93Ser)	NLRC5 (T93S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200509	NM_001384950.1(NLRC5):c.463G>A (p.Ala155Thr)	NLRC5 (A155T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2616707	NM_001384950.1(NLRC5):c.476A>G (p.Tyr159Cys)	NLRC5 (Y159C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2320721	NM_001384950.1(NLRC5):c.482G>A (p.Ser161Asn)	NLRC5 (S161N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2384375	NM_001384950.1(NLRC5):c.550G>A (p.Ala184Thr)	NLRC5 (A184T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2358804	NM_001384950.1(NLRC5):c.595G>A (p.Val199Ile)	NLRC5 (V199I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2222025	NM_001384950.1(NLRC5):c.596T>C (p.Val199Ala)	NLRC5 (V199A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2623089	NM_001384950.1(NLRC5):c.614C>T (p.Ala205Val)	NLRC5 (A205V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2288455	NM_001384950.1(NLRC5):c.659G>A (p.Gly220Asp)	NLRC5 (G220D)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2226221	NM_001384950.1(NLRC5):c.662C>T (p.Pro221Leu)	NLRC5 (P221L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3200514	NM_001384950.1(NLRC5):c.719G>A (p.Arg240Gln)	NLRC5 (R240Q)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2533654	NM_001384950.1(NLRC5):c.748C>G (p.Leu250Val)	NLRC5 (L250V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2375686	NM_001384950.1(NLRC5):c.878A>G (p.Gln293Arg)	NLRC5 (Q236R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2549392	NM_001384950.1(NLRC5):c.1134C>G (p.His378Gln)	NLRC5 (H378Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2346977	NM_001384950.1(NLRC5):c.1154C>T (p.Ser385Leu)	NLRC5 (S385L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3200490	NM_001384950.1(NLRC5):c.1165G>A (p.Ala389Thr)	NLRC5 (A332T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2458338	NM_001384950.1(NLRC5):c.1270G>A (p.Ala424Thr)	NLRC5 (A367T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2356480	NM_001384950.1(NLRC5):c.1303A>G (p.Met435Val)	NLRC5 (M435V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2468237	NM_001384950.1(NLRC5):c.1319T>C (p.Met440Thr)	NLRC5 (M440T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2257698	NM_001384950.1(NLRC5):c.1336C>T (p.Leu446Phe)	NLRC5 (L446F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200492	NM_001384950.1(NLRC5):c.1341C>G (p.Ser447Arg)	NLRC5 (S390R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200493	NM_001384950.1(NLRC5):c.1345C>A (p.Pro449Thr)	NLRC5 (P392T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2372547	NM_001384950.1(NLRC5):c.1345C>G (p.Pro449Ala)	NLRC5 (P392A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2255508	NM_001384950.1(NLRC5):c.1420A>G (p.Ile474Val)	NLRC5 (I474V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2224254	NM_001384950.1(NLRC5):c.1435G>C (p.Asp479His)	NLRC5 (D422H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2311567	NM_001384950.1(NLRC5):c.1447C>T (p.Pro483Ser)	NLRC5 (P483S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200494	NM_001384950.1(NLRC5):c.1619A>G (p.Tyr540Cys)	NLRC5 (Y540C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200495	NM_001384950.1(NLRC5):c.1743G>A (p.Ala581=)	NLRC5	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 2610314	NM_001384950.1(NLRC5):c.2047G>C (p.Val683Leu)	NLRC5 (V626L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2397133	NM_001384950.1(NLRC5):c.2101G>A (p.Ala701Thr)	NLRC5 (A644T +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3200496	NM_001384950.1(NLRC5):c.2140G>T (p.Gly714Trp)	NLRC5 (G657W +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2294707	NM_001384950.1(NLRC5):c.2183C>A (p.Ala728Asp)	NLRC5 (A671D +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2349315	NM_001384950.1(NLRC5):c.2195G>A (p.Ser732Asn)	NLRC5 (S732N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2471704	NM_001384950.1(NLRC5):c.2270A>G (p.Gln757Arg)	NLRC5 (Q700R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2206678	NM_001384950.1(NLRC5):c.2311C>T (p.Arg771Trp)	NLRC5 (R714W +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2282577	NM_001384950.1(NLRC5):c.2312G>A (p.Arg771Gln)	NLRC5 (R743Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200497	NM_001384950.1(NLRC5):c.2318G>A (p.Arg773Gln)	NLRC5 (R773Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3200498	NM_001384950.1(NLRC5):c.2377G>A (p.Val793Met)	NLRC5 (V765M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200499	NM_001384950.1(NLRC5):c.2428C>T (p.Leu810Phe)	NLRC5 (L810F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2316683	NM_001384950.1(NLRC5):c.2447C>T (p.Pro816Leu)	NLRC5 (P759L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200500	NM_001384950.1(NLRC5):c.2461A>T (p.Thr821Ser)	NLRC5 (T821S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2383736	NM_001384950.1(NLRC5):c.2498G>A (p.Ser833Asn)	NLRC5 (S776N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2541482	NM_001384950.1(NLRC5):c.2518G>T (p.Ala840Ser)	NLRC5 (A783S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200501	NM_001384950.1(NLRC5):c.2698G>T (p.Ala900Ser)	NLRC5 (A843S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2598320	NM_001384950.1(NLRC5):c.2771C>T (p.Ala924Val)	NLRC5 (A867V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2395358	NM_001384950.1(NLRC5):c.2875G>A (p.Ala959Thr)	NLRC5 (A931T +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2280515	NM_001384950.1(NLRC5):c.2947C>T (p.His983Tyr)	NLRC5 (H903Y +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2397473	NM_001384950.1(NLRC5):c.3013G>T (p.Gly1005Cys)	NLRC5 (G925C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2520063	NM_001384950.1(NLRC5):c.3014G>T (p.Gly1005Val)	NLRC5 (G1005V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2549393	NM_001384950.1(NLRC5):c.3025C>T (p.Leu1009Phe)	NLRC5 (L929F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2242015	NM_001384950.1(NLRC5):c.3028G>A (p.Asp1010Asn)	NLRC5 (D982N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2486335	NM_001384950.1(NLRC5):c.3034T>C (p.Ser1012Pro)	NLRC5 (S1012P +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200503	NM_001384950.1(NLRC5):c.3168C>G (p.Phe1056Leu)	NLRC5 (F1028L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2607456	NM_001384950.1(NLRC5):c.3173C>T (p.Thr1058Ile)	NLRC5 (T1030I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2278460	NM_001384950.1(NLRC5):c.3256T>C (p.Trp1086Arg)	NLRC5 (W1006R +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2325887	NM_001384950.1(NLRC5):c.3340C>T (p.Leu1114Phe)	NLRC5 (L1056F +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2239697	NM_001384950.1(NLRC5):c.3348G>T (p.Glu1116Asp)	NLRC5 (E1058D +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2213519	NM_001384950.1(NLRC5):c.3432T>G (p.Cys1144Trp)	NLRC5 (C1064W +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2469045	NM_001384950.1(NLRC5):c.3613A>G (p.Thr1205Ala)	NLRC5 (T1175A +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2589891	NM_001384950.1(NLRC5):c.3621C>G (p.His1207Gln)	NLRC5 (H1149Q +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2296889	NM_001384950.1(NLRC5):c.3732C>A (p.Asp1244Glu)	NLRC5 (D1185E +6 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2297944	NM_001384950.1(NLRC5):c.3766G>T (p.Gly1256Cys)	NLRC5 (G1197C +6 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3200504	NM_001384950.1(NLRC5):c.3799C>G (p.Leu1267Val)	NLRC5 (L1266V +6 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2238765	NM_001384950.1(NLRC5):c.3865C>A (p.Leu1289Met)	NLRC5 (L1258M +7 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2555034	NM_001384950.1(NLRC5):c.3866T>C (p.Leu1289Pro)	NLRC5 (L1180P +7 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2285954	NM_001384950.1(NLRC5):c.3890C>A (p.Ser1297Tyr)	NLRC5 (S1188Y +7 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2380427	NM_001384950.1(NLRC5):c.3899G>A (p.Arg1300His)	NLRC5 (R1299H +7 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3200505	NM_001384950.1(NLRC5):c.3904C>T (p.Arg1302Trp)	NLRC5 (R1271W +7 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3200506	NM_001384950.1(NLRC5):c.4033A>G (p.Thr1345Ala)	LOC126862362, NLRC5 (T1286A +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2543280	NM_001384950.1(NLRC5):c.4147A>G (p.Ser1383Gly)	LOC126862362, NLRC5 (S1324G +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2204902	NM_001384950.1(NLRC5):c.4184G>C (p.Arg1395Thr)	NLRC5 (R1394T +5 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2338544	NM_001384950.1(NLRC5):c.4385G>A (p.Cys1462Tyr)	NLRC5 (C1403Y +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2399978	NM_001384950.1(NLRC5):c.4387G>C (p.Ala1463Pro)	NLRC5 (A1404P +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2615637	NM_001384950.1(NLRC5):c.4575G>T (p.Glu1525Asp)	NLRC5 (E1467D +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2364087	NM_001384950.1(NLRC5):c.4579C>G (p.Leu1527Val)	NLRC5 (L1499V +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200508	NM_001384950.1(NLRC5):c.4622C>T (p.Ala1541Val)	NLRC5 (A1513V +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2263915	NM_001384950.1(NLRC5):c.4643G>A (p.Gly1548Glu)	NLRC5 (G1489E +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2457771	NM_001384950.1(NLRC5):c.4703C>T (p.Ala1568Val)	NLRC5 (A1538V +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2270672	NM_001384950.1(NLRC5):c.4715A>T (p.His1572Leu)	NLRC5 (H1572L +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2349501	NM_001384950.1(NLRC5):c.4771G>A (p.Gly1591Ser)	NLRC5 (G1591S +6 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2349797	NM_001384950.1(NLRC5):c.4792C>A (p.Leu1598Ile)	NLRC5 (L1568I +6 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2460353	NM_001384950.1(NLRC5):c.4807A>G (p.Arg1603Gly)	NLRC5 (R1573G +6 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2292239	NM_001384950.1(NLRC5):c.4987C>T (p.Arg1663Cys)	NLRC5 (R1605C +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200510	NM_001384950.1(NLRC5):c.5074G>A (p.Val1692Ile)	NLRC5 (V1633I +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2212361	NM_001384950.1(NLRC5):c.5087C>A (p.Pro1696Gln)	NLRC5 (P1667Q +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200511	NM_001384950.1(NLRC5):c.5144C>T (p.Ser1715Phe)	NLRC5 (S1656F +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2462222	NM_001384950.1(NLRC5):c.5147C>T (p.Pro1716Leu)	NLRC5 (P1657L +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2206651	NM_001384950.1(NLRC5):c.5443C>T (p.Leu1815Phe)	NLRC5 (L1757F +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2204861	NM_001384950.1(NLRC5):c.5518A>G (p.Met1840Val)	NLRC5 (M1782V +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2300555	NM_001384950.1(NLRC5):c.5520G>A (p.Met1840Ile)	NLRC5 (M1782I +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 97