"Ambry Genetics"[submitter] AND "SLIT3"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2304880	NM_003062.4(SLIT3):c.4561G>A (p.Ala1521Thr)	SLIT3 (A1528T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309060	NM_003062.4(SLIT3):c.4558C>T (p.Leu1520Phe)	SLIT3 (L1527F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592505	NM_003062.4(SLIT3):c.4552G>A (p.Gly1518Ser)	SLIT3 (G1518S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2388206	NM_003062.4(SLIT3):c.4481G>A (p.Arg1494Gln)	SLIT3 (R1494Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349765	NM_003062.4(SLIT3):c.4472G>A (p.Arg1491His)	SLIT3 (R1491H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166060	NM_003062.4(SLIT3):c.4436G>A (p.Arg1479His)	SLIT3 (R1486H +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3166059	NM_003062.4(SLIT3):c.4378C>T (p.Arg1460Cys)	SLIT3 (R1460C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2282496	NM_003062.4(SLIT3):c.4361T>G (p.Val1454Gly)	SLIT3 (V1454G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486285	NM_003062.4(SLIT3):c.4343C>T (p.Pro1448Leu)	SLIT3 (P1455L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2405646	NM_003062.4(SLIT3):c.4309G>A (p.Gly1437Ser)	SLIT3 (G1437S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494787	NM_003062.4(SLIT3):c.4289C>T (p.Pro1430Leu)	SLIT3 (P1430L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462045	NM_003062.4(SLIT3):c.4247A>G (p.Lys1416Arg)	SLIT3 (K1416R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166058	NM_003062.4(SLIT3):c.4196G>A (p.Gly1399Glu)	SLIT3 (G1406E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318859	NM_003062.4(SLIT3):c.4154C>A (p.Thr1385Asn)	SLIT3 (T1392N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166057	NM_003062.4(SLIT3):c.4097A>G (p.Gln1366Arg)	SLIT3 (Q1366R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206469	NM_003062.4(SLIT3):c.4044G>T (p.Lys1348Asn)	SLIT3 (K1348N +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2252374	NM_003062.4(SLIT3):c.3971A>C (p.Gln1324Pro)	SLIT3 (Q1331P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166056	NM_003062.4(SLIT3):c.3947A>T (p.Gln1316Leu)	SLIT3 (Q1316L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2320730	NM_003062.4(SLIT3):c.3923A>T (p.Glu1308Val)	SLIT3 (E1315V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404023	NM_003062.4(SLIT3):c.3859G>A (p.Gly1287Ser)	SLIT3 (G1287S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2228265	NM_003062.4(SLIT3):c.3742C>A (p.Gln1248Lys)	SLIT3 (Q1248K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283455	NM_003062.4(SLIT3):c.3602A>G (p.Asn1201Ser)	SLIT3 (N1208S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535594	NM_003062.4(SLIT3):c.3566A>C (p.Asp1189Ala)	SLIT3 (D1189A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2492976	NM_003062.4(SLIT3):c.3556G>A (p.Val1186Met)	SLIT3 (V1193M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2591558	NM_003062.4(SLIT3):c.3478G>A (p.Val1160Ile)	SLIT3 (V1167I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2603994	NM_003062.4(SLIT3):c.3454C>T (p.Pro1152Ser)	SLIT3 (P1159S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 809840	NM_003062.4(SLIT3):c.3365C>A (p.Pro1122Gln)	SLIT3 (P1129Q +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 3166052	NM_003062.4(SLIT3):c.3333C>A (p.His1111Gln)	SLIT3 (H1118Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2609614	NM_003062.4(SLIT3):c.3296C>T (p.Thr1099Ile)	SLIT3 (T1099I +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2380333	NM_003062.4(SLIT3):c.3233G>A (p.Cys1078Tyr)	SLIT3 (C1078Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166051	NM_003062.4(SLIT3):c.3230A>G (p.Asp1077Gly)	SLIT3 (D1077G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318673	NM_003062.4(SLIT3):c.3123G>C (p.Glu1041Asp)	SLIT3 (E1041D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166049	NM_003062.4(SLIT3):c.3055G>A (p.Val1019Met)	SLIT3 (V1019M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166048	NM_003062.4(SLIT3):c.3053A>T (p.Tyr1018Phe)	SLIT3 (Y1018F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306870	NM_003062.4(SLIT3):c.3004G>A (p.Asp1002Asn)	SLIT3 (D1009N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2620940	NM_003062.4(SLIT3):c.2995G>A (p.Asp999Asn)	SLIT3 (D1006N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363096	NM_003062.4(SLIT3):c.2975G>A (p.Arg992Gln)	SLIT3 (R999Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242106	NM_003062.4(SLIT3):c.2860G>A (p.Val954Met)	SLIT3 (V961M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166047	NM_003062.4(SLIT3):c.2654G>A (p.Ser885Asn)	SLIT3, SLIT3-AS2 (S885N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380260	NM_003062.4(SLIT3):c.2621C>T (p.Ala874Val)	SLIT3, SLIT3-AS2 (A874V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241457	NM_003062.4(SLIT3):c.2531A>G (p.Asn844Ser)	LOC126807585, SLIT3 +1 more (N844S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3166046	NM_003062.4(SLIT3):c.2447T>C (p.Val816Ala)	SLIT3 (V816A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166045	NM_003062.4(SLIT3):c.2394G>A (p.Met798Ile)	SLIT3 (M798I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2441867	NM_003062.4(SLIT3):c.2393T>C (p.Met798Thr)	SLIT3 (M798T)	Single nucleotide variant (missense variant)	SLIT3-related anomalies of the kidney and urinary tract +1 more	GUncertain significance
Select item 2277223	NM_003062.4(SLIT3):c.2333C>T (p.Thr778Met)	SLIT3 (T778M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166044	NM_003062.4(SLIT3):c.2317G>A (p.Ala773Thr)	SLIT3 (A773T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353852	NM_003062.4(SLIT3):c.2233G>A (p.Ala745Thr)	SLIT3 (A745T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166043	NM_003062.4(SLIT3):c.2206G>A (p.Val736Met)	SLIT3 (V736M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2205129	NM_003062.4(SLIT3):c.2129C>T (p.Thr710Ile)	SLIT3 (T710I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222900	NM_003062.4(SLIT3):c.2042G>A (p.Arg681Lys)	SLIT3 (R681K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2234707	NM_003062.4(SLIT3):c.2039A>T (p.Lys680Met)	SLIT3 (K680M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215399	NM_003062.4(SLIT3):c.1952C>T (p.Thr651Met)	SLIT3 (T651M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166041	NM_003062.4(SLIT3):c.1934C>A (p.Thr645Asn)	SLIT3 (T645N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358520	NM_003062.4(SLIT3):c.1879G>A (p.Gly627Ser)	SLIT3 (G627S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618589	NM_003062.4(SLIT3):c.1819C>A (p.Leu607Ile)	SLIT3 (L607I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396399	NM_003062.4(SLIT3):c.1747G>A (p.Val583Met)	SLIT3 (V583M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286849	NM_003062.4(SLIT3):c.1732G>A (p.Asp578Asn)	SLIT3 (D578N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166040	NM_003062.4(SLIT3):c.1679G>A (p.Arg560Gln)	SLIT3 (R560Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166039	NM_003062.4(SLIT3):c.1678C>T (p.Arg560Trp)	SLIT3 (R560W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275682	NM_003062.4(SLIT3):c.1669C>G (p.Pro557Ala)	SLIT3 (P557A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521061	NM_003062.4(SLIT3):c.1582A>G (p.Ser528Gly)	SLIT3 (S528G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551451	NM_003062.4(SLIT3):c.1492G>A (p.Glu498Lys)	SLIT3 (E498K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166038	NM_003062.4(SLIT3):c.1482G>T (p.Arg494Ser)	SLIT3 (R494S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525761	NM_003062.4(SLIT3):c.1421G>A (p.Arg474His)	SLIT3 (R474H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166036	NM_003062.4(SLIT3):c.1382G>T (p.Gly461Val)	SLIT3 (G461V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2237060	NM_003062.4(SLIT3):c.1372G>A (p.Glu458Lys)	SLIT3 (E458K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361958	NM_003062.4(SLIT3):c.1270G>A (p.Ala424Thr)	SLIT3 (A424T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536310	NM_003062.4(SLIT3):c.1217A>C (p.Asn406Thr)	SLIT3 (N406T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166035	NM_003062.4(SLIT3):c.1212C>G (p.Asn404Lys)	SLIT3 (N404K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517535	NM_003062.4(SLIT3):c.1145A>G (p.Gln382Arg)	LOC126807586, SLIT3 (Q382R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469848	NM_003062.4(SLIT3):c.1105G>A (p.Glu369Lys)	LOC126807586, SLIT3 (E369K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166034	NM_003062.4(SLIT3):c.1033G>C (p.Asp345His)	SLIT3 (D345H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330314	NM_003062.4(SLIT3):c.1027A>G (p.Ile343Val)	SLIT3 (I343V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208930	NM_003062.4(SLIT3):c.962C>G (p.Ala321Gly)	SLIT3 (A321G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2406743	NM_003062.4(SLIT3):c.955A>T (p.Ile319Phe)	SLIT3 (I319F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463490	NM_003062.4(SLIT3):c.896T>C (p.Met299Thr)	SLIT3 (M299T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2332164	NM_003062.4(SLIT3):c.895A>G (p.Met299Val)	SLIT3 (M299V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348638	NM_003062.4(SLIT3):c.871G>A (p.Val291Met)	SLIT3 (V291M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217874	NM_003062.4(SLIT3):c.845C>T (p.Ser282Leu)	SLIT3 (S282L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225546	NM_003062.4(SLIT3):c.799C>T (p.His267Tyr)	SLIT3 (H267Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2300488	NM_003062.4(SLIT3):c.784G>A (p.Val262Met)	SLIT3 (V262M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2224840	NM_003062.4(SLIT3):c.761C>T (p.Ala254Val)	SLIT3 (A254V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166063	NM_003062.4(SLIT3):c.730G>A (p.Ala244Thr)	SLIT3 (A244T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378207	NM_003062.4(SLIT3):c.583C>T (p.Arg195Cys)	LOC126807587, SLIT3 (R195C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166062	NM_003062.4(SLIT3):c.523G>A (p.Gly175Arg)	SLIT3 (G175R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2278207	NM_003062.4(SLIT3):c.475G>A (p.Val159Met)	SLIT3 (V159M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2260494	NM_003062.4(SLIT3):c.446C>G (p.Pro149Arg)	SLIT3 (P149R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2288463	NM_003062.4(SLIT3):c.437A>G (p.Gln146Arg)	SLIT3 (Q146R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223355	NM_003062.4(SLIT3):c.437A>T (p.Gln146Leu)	SLIT3 (Q146L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2455253	NM_003062.4(SLIT3):c.395C>T (p.Thr132Met)	SLIT3 (T132M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166055	NM_003062.4(SLIT3):c.379T>A (p.Leu127Met)	SLIT3 (L127M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166054	NM_003062.4(SLIT3):c.358A>G (p.Lys120Glu)	SLIT3 (K120E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218362	NM_003062.4(SLIT3):c.343C>T (p.Arg115Cys)	SLIT3 (R115C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613565	NM_003062.4(SLIT3):c.342G>T (p.Leu114=)	SLIT3	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3166053	NM_003062.4(SLIT3):c.338G>A (p.Arg113Gln)	SLIT3 (R113Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166050	NM_003062.4(SLIT3):c.311C>G (p.Ala104Gly)	SLIT3 (A104G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273473	NM_003062.4(SLIT3):c.280G>A (p.Asp94Asn)	SLIT3 (D94N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390153	NM_003062.4(SLIT3):c.263G>A (p.Arg88Gln)	SLIT3 (R88Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2570092	NM_003062.4(SLIT3):c.241T>C (p.Phe81Leu)	SLIT3 (F81L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2288389	NM_003062.4(SLIT3):c.173G>T (p.Gly58Val)	SLIT3 (G58V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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