ClinVar for Gene (Select 6586) - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 1 to 100 of 207

<< First< Prev

Page of 3

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3355894	NM_003062.4(SLIT3):c.1913A>G (p.Asp638Gly)	SLIT3 (D638G)	Single nucleotide variant (missense variant)	SLIT3-related disorder	GUncertain significance
Select item 3348691	NM_003062.4(SLIT3):c.1039G>T (p.Ala347Ser)	SLIT3 (A347S)	Single nucleotide variant (missense variant)	SLIT3-related disorder	GUncertain significance
Select item 3320525	NM_003062.4(SLIT3):c.908C>G (p.Ala303Gly)	SLIT3 (A303G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320524	NM_003062.4(SLIT3):c.1381G>A (p.Gly461Arg)	SLIT3 (G461R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320523	NM_003062.4(SLIT3):c.3449C>T (p.Ala1150Val)	SLIT3 (A1157V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320522	NM_003062.4(SLIT3):c.1469A>G (p.Asp490Gly)	SLIT3 (D490G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320521	NM_003062.4(SLIT3):c.1889C>T (p.Ser630Leu)	SLIT3 (S630L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320520	NM_003062.4(SLIT3):c.3455C>T (p.Pro1152Leu)	SLIT3 (P1152L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320519	NM_003062.4(SLIT3):c.614C>A (p.Pro205Gln)	LOC126807587, SLIT3 (P205Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320517	NM_003062.4(SLIT3):c.2375A>G (p.Asn792Ser)	SLIT3 (N792S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320516	NM_003062.4(SLIT3):c.1243C>A (p.Leu415Met)	SLIT3 (L415M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320515	NM_003062.4(SLIT3):c.2726T>G (p.Val909Gly)	SLIT3, SLIT3-AS2 (V916G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320514	NM_003062.4(SLIT3):c.1537G>A (p.Gly513Ser)	SLIT3 (G513S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320513	NM_003062.4(SLIT3):c.3757G>A (p.Val1253Ile)	SLIT3 (V1253I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320512	NM_003062.4(SLIT3):c.3094G>A (p.Asp1032Asn)	SLIT3 (D1039N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320511	NM_003062.4(SLIT3):c.509G>A (p.Ser170Asn)	SLIT3 (S170N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320510	NM_003062.4(SLIT3):c.4106G>A (p.Arg1369Gln)	SLIT3 (R1369Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166064	NM_003062.4(SLIT3):c.94G>C (p.Val32Leu)	SLIT3 (V32L)	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 3166062	NM_003062.4(SLIT3):c.523G>A (p.Gly175Arg)	SLIT3 (G175R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166061	NM_003062.4(SLIT3):c.44G>A (p.Arg15His)	SLIT3 (R15H)	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 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 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 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 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 3166053	NM_003062.4(SLIT3):c.338G>A (p.Arg113Gln)	SLIT3 (R113Q)	Single nucleotide variant (missense variant)	not specified	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 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 3166050	NM_003062.4(SLIT3):c.311C>G (p.Ala104Gly)	SLIT3 (A104G)	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 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 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 3166044	NM_003062.4(SLIT3):c.2317G>A (p.Ala773Thr)	SLIT3 (A773T)	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 3166042	NM_003062.4(SLIT3):c.20G>A (p.Gly7Glu)	SLIT3 (G7E)	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 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 3166038	NM_003062.4(SLIT3):c.1482G>T (p.Arg494Ser)	SLIT3 (R494S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166037	NM_003062.4(SLIT3):c.145G>T (p.Gly49Trp)	SLIT3 (G49W)	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 3166035	NM_003062.4(SLIT3):c.1212C>G (p.Asn404Lys)	SLIT3 (N404K)	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 3062853	GRCh37/hg19 5q34-35.1(chr5:167580162-168867423)x1	MIR103A1, PANK3 +4 more	Copy number loss	not specified	GUncertain significance
Select item 3062837	GRCh37/hg19 5q34-35.1(chr5:165763259-170909410)x1	C5orf58, DOCK2 +18 more	Copy number loss	not specified	GPathogenic
Select item 3056199	NM_003062.4(SLIT3):c.699A>G (p.Arg233=)	SLIT3	Single nucleotide variant (synonymous variant)	SLIT3-related disorder	GLikely benign
Select item 3047769	NM_003062.4(SLIT3):c.3088C>T (p.Leu1030=)	SLIT3	Single nucleotide variant (synonymous variant)	SLIT3-related disorder	GLikely benign
Select item 3047539	NM_003062.4(SLIT3):c.1804C>T (p.Arg602Cys)	SLIT3 (R602C)	Single nucleotide variant (missense variant)	SLIT3-related disorder	GLikely benign
Select item 3046000	NM_003062.4(SLIT3):c.937C>T (p.Arg313Cys)	SLIT3 (R313C)	Single nucleotide variant (missense variant)	SLIT3-related disorder	GLikely benign
Select item 3040777	NM_003062.4(SLIT3):c.3903C>T (p.Gly1301=)	SLIT3	Single nucleotide variant (synonymous variant)	SLIT3-related disorder	GBenign
Select item 3034009	NM_003062.4(SLIT3):c.2333C>A (p.Thr778Lys)	SLIT3 (T778K)	Single nucleotide variant (missense variant)	SLIT3-related disorder	GUncertain significance
Select item 3029294	NM_003062.4(SLIT3):c.2991A>G (p.Pro997=)	SLIT3	Single nucleotide variant (synonymous variant)	SLIT3-related disorder	GLikely benign
Select item 3026026	NM_003062.4(SLIT3):c.804G>A (p.Ser268=)	SLIT3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3024729	NM_003062.4(SLIT3):c.1481G>C (p.Arg494Thr)	SLIT3 (R494T)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2685182	GRCh37/hg19 5q34(chr5:163825772-168355129)x1	MIR103A1, PANK3 +4 more	Copy number loss	not provided	GUncertain significance
Select item 2656063	NM_003062.4(SLIT3):c.855G>A (p.Thr285=)	SLIT3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656062	NM_003062.4(SLIT3):c.1323C>T (p.Cys441=)	SLIT3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656061	NM_003062.4(SLIT3):c.1464C>T (p.Ser488=)	SLIT3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656060	NM_003062.4(SLIT3):c.1475G>A (p.Arg492His)	SLIT3 (R492H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2656059	NM_003062.4(SLIT3):c.1506C>T (p.Asp502=)	SLIT3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656058	NM_003062.4(SLIT3):c.1509C>T (p.Leu503=)	SLIT3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656057	NM_003062.4(SLIT3):c.1785C>T (p.Thr595=)	SLIT3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656056	NM_003062.4(SLIT3):c.1990C>A (p.Pro664Thr)	SLIT3 (P664T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2656055	NM_003062.4(SLIT3):c.2559G>A (p.Ala853=)	SLIT3, SLIT3-AS2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656054	NM_003062.4(SLIT3):c.2805T>C (p.Pro935=)	SLIT3, SLIT3-AS2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656053	NM_003062.4(SLIT3):c.2874C>T (p.Thr958=)	SLIT3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656052	NM_003062.4(SLIT3):c.3096C>T (p.Asp1032=)	SLIT3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656051	NM_003062.4(SLIT3):c.3204G>A (p.Gly1068=)	SLIT3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656050	NM_003062.4(SLIT3):c.3268G>A (p.Val1090Met)	SLIT3 (V1090M +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2656049	NM_003062.4(SLIT3):c.3540C>T (p.Ala1180=)	SLIT3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656048	NM_003062.4(SLIT3):c.3783C>T (p.Ser1261=)	SLIT3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656047	NM_003062.4(SLIT3):c.3960C>A (p.Ala1320=)	SLIT3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656046	NM_003062.4(SLIT3):c.4053G>A (p.Val1351=)	SLIT3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656045	NM_003062.4(SLIT3):c.4165T>C (p.Tyr1389His)	SLIT3 (Y1389H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2656044	NM_003062.4(SLIT3):c.4321G>A (p.Glu1441Lys)	SLIT3 (E1441K +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2656043	NM_003062.4(SLIT3):c.4506G>A (p.Thr1502=)	SLIT3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2635824	NM_003062.4(SLIT3):c.10_17del	SLIT3	Deletion (3 prime UTR variant)	SLIT3-related disorder	GUncertain significance
Select item 2635033	NM_003062.4(SLIT3):c.4455G>T (p.Gln1485His)	SLIT3 (Q1485H +1 more)	Single nucleotide variant (missense variant)	SLIT3-related disorder	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 2618589	NM_003062.4(SLIT3):c.1819C>A (p.Leu607Ile)	SLIT3 (L607I)	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 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 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 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 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 2582364	NM_003062.4(SLIT3):c.691C>T (p.Arg231Ter)	SLIT3 (R231*)	Single nucleotide variant (nonsense)	SLIT3-related anomalies of the kidney and urinary tract	GUncertain significance
Select item 2582303	NM_003062.4(SLIT3):c.1604C>A (p.Thr535Asn)	SLIT3 (T535N)	Single nucleotide variant (missense variant)	SLIT3-related anomalies of the kidney and urinary tract	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 2551451	NM_003062.4(SLIT3):c.1492G>A (p.Glu498Lys)	SLIT3 (E498K)	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 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 2525761	NM_003062.4(SLIT3):c.1421G>A (p.Arg474His)	SLIT3 (R474H)	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 2517535	NM_003062.4(SLIT3):c.1145A>G (p.Gln382Arg)	LOC126807586, SLIT3 (Q382R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2498992	NM_003062.4(SLIT3):c.2643C>T (p.Ile881=)	SLIT3, SLIT3-AS2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

<< First< Prev

Page of 3