"Ambry Genetics"[submitter] AND "NLRC3"[gene] - ClinVar

Search results

Items: 83

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2379430	NM_178844.4(NLRC3):c.3137G>A (p.Gly1046Glu)	NLRC3 (G1046E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2267133	NM_178844.4(NLRC3):c.2812G>A (p.Val938Met)	NLRC3 (V938M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2483789	NM_178844.4(NLRC3):c.2422C>G (p.Leu808Val)	NLRC3 (L808V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2283150	NM_178844.4(NLRC3):c.2287G>A (p.Gly763Arg)	NLRC3 (G763R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2395819	NM_178844.4(NLRC3):c.2230G>A (p.Glu744Lys)	NLRC3 (E744K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2358303	NM_178844.4(NLRC3):c.2219G>C (p.Arg740Thr)	NLRC3 (R740T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2483042	NM_178844.4(NLRC3):c.2191G>A (p.Gly731Ser)	NLRC3 (G731S)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2412125	NM_178844.4(NLRC3):c.2173A>G (p.Thr725Ala)	NLRC3 (T725A)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2254521	NM_178844.4(NLRC3):c.2165G>A (p.Arg722His)	NLRC3 (R722H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200471	NM_178844.4(NLRC3):c.2164C>T (p.Arg722Cys)	NLRC3 (R722C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2311566	NM_178844.4(NLRC3):c.2164C>G (p.Arg722Gly)	NLRC3 (R722G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2298346	NM_178844.4(NLRC3):c.2157G>T (p.Lys719Asn)	NLRC3 (K719N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2475073	NM_178844.4(NLRC3):c.2138C>A (p.Ala713Glu)	NLRC3 (A713E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200468	NM_178844.4(NLRC3):c.2069T>C (p.Leu690Pro)	NLRC3 (L690P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3299977	NM_178844.4(NLRC3):c.1999C>A (p.Arg667Ser)	NLRC3 (R667S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3299983	NM_178844.4(NLRC3):c.1953C>A (p.Asp651Glu)	NLRC3 (D651E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2509674	NM_178844.4(NLRC3):c.1837G>T (p.Ala613Ser)	NLRC3 (A613S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200467	NM_178844.4(NLRC3):c.1823T>C (p.Leu608Pro)	NLRC3 (L608P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200466	NM_178844.4(NLRC3):c.1808C>T (p.Ala603Val)	NLRC3 (A603V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200465	NM_178844.4(NLRC3):c.1789G>A (p.Gly597Ser)	NLRC3 (G597S)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3200464	NM_178844.4(NLRC3):c.1738G>T (p.Ala580Ser)	NLRC3 (A580S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2302495	NM_178844.4(NLRC3):c.1732G>C (p.Glu578Gln)	NLRC3 (E578Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3299980	NM_178844.4(NLRC3):c.1688G>A (p.Arg563Gln)	NLRC3 (R563Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2254605	NM_178844.4(NLRC3):c.1663C>T (p.Arg555Cys)	NLRC3 (R555C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3299986	NM_178844.4(NLRC3):c.1657T>G (p.Cys553Gly)	NLRC3 (C553G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2244344	NM_178844.4(NLRC3):c.1636G>A (p.Val546Met)	NLRC3 (V546M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200463	NM_178844.4(NLRC3):c.1627C>T (p.Arg543Trp)	NLRC3 (R543W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2618015	NM_178844.4(NLRC3):c.1595C>T (p.Ser532Phe)	NLRC3 (S532F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3299978	NM_178844.4(NLRC3):c.1591G>A (p.Gly531Ser)	NLRC3 (G531S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2270526	NM_178844.4(NLRC3):c.1588G>A (p.Ala530Thr)	NLRC3 (A530T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2555012	NM_178844.4(NLRC3):c.1580C>T (p.Ala527Val)	NLRC3 (A527V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200462	NM_178844.4(NLRC3):c.1577A>G (p.Asn526Ser)	NLRC3 (N526S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200461	NM_178844.4(NLRC3):c.1555G>A (p.Gly519Ser)	NLRC3 (G519S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200459	NM_178844.4(NLRC3):c.1550T>C (p.Leu517Pro)	NLRC3 (L517P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200458	NM_178844.4(NLRC3):c.1472T>C (p.Phe491Ser)	NLRC3 (F491S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2624070	NM_178844.4(NLRC3):c.1408G>C (p.Ala470Pro)	NLRC3 (A470P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2552106	NM_178844.4(NLRC3):c.1340C>T (p.Ser447Leu)	NLRC3 (S447L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2234422	NM_178844.4(NLRC3):c.1325A>G (p.Glu442Gly)	NLRC3 (E442G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2455935	NM_178844.4(NLRC3):c.1322G>A (p.Arg441Lys)	NLRC3 (R441K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200457	NM_178844.4(NLRC3):c.1268T>C (p.Phe423Ser)	NLRC3 (F423S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2368160	NM_178844.4(NLRC3):c.1258A>G (p.Met420Val)	NLRC3 (M420V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200456	NM_178844.4(NLRC3):c.1196C>T (p.Thr399Ile)	NLRC3 (T399I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2272065	NM_178844.4(NLRC3):c.1162C>G (p.Gln388Glu)	NLRC3 (Q388E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3299979	NM_178844.4(NLRC3):c.1158C>G (p.Ile386Met)	NLRC3 (I386M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2381626	NM_178844.4(NLRC3):c.1112C>T (p.Ala371Val)	NLRC3 (A371V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3299981	NM_178844.4(NLRC3):c.1111G>A (p.Ala371Thr)	NLRC3 (A371T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2359242	NM_178844.4(NLRC3):c.1040C>T (p.Thr347Met)	NLRC3 (T347M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2206276	NM_178844.4(NLRC3):c.1030C>T (p.Arg344Cys)	NLRC3 (R344C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2595200	NM_178844.4(NLRC3):c.1004C>T (p.Thr335Met)	NLRC3 (T335M)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2389027	NM_178844.4(NLRC3):c.980C>G (p.Thr327Ser)	NLRC3 (T327S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2338659	NM_178844.4(NLRC3):c.917A>C (p.Gln306Pro)	NLRC3 (Q306P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200481	NM_178844.4(NLRC3):c.851C>T (p.Thr284Met)	NLRC3 (T284M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3299982	NM_178844.4(NLRC3):c.815C>G (p.Ser272Cys)	NLRC3 (S272C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2258843	NM_178844.4(NLRC3):c.805C>T (p.Pro269Ser)	NLRC3 (P269S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2241496	NM_178844.4(NLRC3):c.800C>T (p.Ser267Phe)	NLRC3 (S267F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2209225	NM_178844.4(NLRC3):c.776C>T (p.Pro259Leu)	NLRC3 (P259L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200480	NM_178844.4(NLRC3):c.769C>T (p.Leu257Phe)	NLRC3 (L257F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3299985	NM_178844.4(NLRC3):c.731C>T (p.Pro244Leu)	NLRC3 (P244L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2615380	NM_178844.4(NLRC3):c.731C>G (p.Pro244Arg)	NLRC3 (P244R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2468092	NM_178844.4(NLRC3):c.721A>G (p.Lys241Glu)	NLRC3 (K241E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200478	NM_178844.4(NLRC3):c.710C>T (p.Thr237Met)	NLRC3 (T237M)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2487206	NM_178844.4(NLRC3):c.700G>A (p.Val234Met)	NLRC3 (V234M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200477	NM_178844.4(NLRC3):c.692C>T (p.Ser231Phe)	NLRC3 (S231F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2483994	NM_178844.4(NLRC3):c.614G>C (p.Ser205Thr)	NLRC3 (S205T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3299976	NM_178844.4(NLRC3):c.596C>T (p.Pro199Leu)	NLRC3 (P199L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2466483	NM_178844.4(NLRC3):c.539G>A (p.Arg180Gln)	NLRC3 (R180Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2307599	NM_178844.4(NLRC3):c.538C>T (p.Arg180Trp)	NLRC3 (R180W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200476	NM_178844.4(NLRC3):c.520G>A (p.Val174Met)	NLRC3 (V174M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200475	NM_178844.4(NLRC3):c.426C>G (p.Ile142Met)	NLRC3 (I142M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2521461	NM_178844.4(NLRC3):c.409C>T (p.Pro137Ser)	NLRC3 (P137S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2359812	NM_178844.4(NLRC3):c.397C>T (p.Arg133Trp)	NLRC3 (R133W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200474	NM_178844.4(NLRC3):c.389C>T (p.Pro130Leu)	NLRC3 (P130L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2382458	NM_178844.4(NLRC3):c.346G>A (p.Gly116Arg)	NLRC3 (G116R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2461817	NM_178844.4(NLRC3):c.337C>T (p.Arg113Cys)	NLRC3 (R113C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200473	NM_178844.4(NLRC3):c.331G>A (p.Ala111Thr)	NLRC3 (A111T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2326699	NM_178844.4(NLRC3):c.313G>A (p.Asp105Asn)	NLRC3 (D105N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2374452	NM_178844.4(NLRC3):c.242G>A (p.Gly81Asp)	NLRC3 (G81D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2350207	NM_178844.4(NLRC3):c.127C>A (p.Pro43Thr)	NLRC3 (P43T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2235707	NM_178844.4(NLRC3):c.87G>C (p.Met29Ile)	NLRC3 (M29I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2610264	NM_178844.4(NLRC3):c.56G>T (p.Gly19Val)	NLRC3 (G19V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2518408	NM_178844.4(NLRC3):c.23C>T (p.Thr8Met)	NLRC3 (T8M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2363792	NM_178844.4(NLRC3):c.20G>T (p.Arg7Leu)	NLRC3 (R7L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2309556	NM_178844.4(NLRC3):c.20G>A (p.Arg7Gln)	NLRC3 (R7Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar

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Items: 83