LMTK3[gene] and "single gene"[properties] - ClinVar

Search results

Items: 94

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3291022	NM_001388485.1(LMTK3):c.4211G>T (p.Ser1404Ile)	LMTK3 (S1404I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291014	NM_001388485.1(LMTK3):c.4154C>T (p.Thr1385Met)	LMTK3 (T1385M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217176	NM_001388485.1(LMTK3):c.4127C>G (p.Pro1376Arg)	LMTK3 (P1376R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119444	NM_001388485.1(LMTK3):c.3959C>A (p.Ala1320Glu)	LMTK3 (A1320E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522007	NM_001388485.1(LMTK3):c.3880C>G (p.Pro1294Ala)	LMTK3 (P1294A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2335039	NM_001388485.1(LMTK3):c.3865G>A (p.Glu1289Lys)	LMTK3 (E1289K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3042586	NM_001388485.1(LMTK3):c.3855GGA[2] (p.Glu1287del)	LMTK3 (E1287del)	Microsatellite (inframe deletion)	LMTK3-related disorder	GLikely benign
Select item 2594336	NM_001388485.1(LMTK3):c.3841G>A (p.Glu1281Lys)	LMTK3 (E1281K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2465084	NM_001388485.1(LMTK3):c.3833G>A (p.Gly1278Glu)	LMTK3 (G1278E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487833	NM_001388485.1(LMTK3):c.3809C>A (p.Ala1270Glu)	LMTK3 (A1270E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2569374	NM_001388485.1(LMTK3):c.3781G>C (p.Ala1261Pro)	LMTK3 (A1261P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292222	NM_001388485.1(LMTK3):c.3778G>T (p.Ala1260Ser)	LMTK3 (A1260S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119443	NM_001388485.1(LMTK3):c.3743C>T (p.Pro1248Leu)	LMTK3 (P1248L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2559681	NM_001388485.1(LMTK3):c.3727T>C (p.Phe1243Leu)	LMTK3 (F1243L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2569373	NM_001388485.1(LMTK3):c.3680G>A (p.Arg1227Lys)	LMTK3 (R1227K)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2356177	NM_001388485.1(LMTK3):c.3656G>A (p.Gly1219Glu)	LMTK3 (G1219E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291017	NM_001388485.1(LMTK3):c.3613C>G (p.Pro1205Ala)	LMTK3 (P1205A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119442	NM_001388485.1(LMTK3):c.3605G>A (p.Arg1202Lys)	LMTK3 (R1202K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525117	NM_001388485.1(LMTK3):c.3588C>A (p.Asp1196Glu)	LMTK3 (D1196E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382077	NM_001388485.1(LMTK3):c.3583G>A (p.Gly1195Arg)	LMTK3 (G1195R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119441	NM_001388485.1(LMTK3):c.3566C>T (p.Thr1189Met)	LMTK3 (T1189M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119440	NM_001388485.1(LMTK3):c.3556G>A (p.Gly1186Ser)	LMTK3 (G1186S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2236896	NM_001388485.1(LMTK3):c.3449T>C (p.Leu1150Pro)	LMTK3 (L1150P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2282673	NM_001388485.1(LMTK3):c.3437C>A (p.Pro1146Gln)	LMTK3 (P1146Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595991	NM_001388485.1(LMTK3):c.3422C>G (p.Thr1141Arg)	LMTK3 (T1141R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345660	NM_001388485.1(LMTK3):c.3403G>T (p.Ala1135Ser)	LMTK3 (A1135S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356176	NM_001388485.1(LMTK3):c.3374G>A (p.Gly1125Asp)	LMTK3 (G1125D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2300451	NM_001388485.1(LMTK3):c.3370G>A (p.Gly1124Ser)	LMTK3 (G1124S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291018	NM_001388485.1(LMTK3):c.3286G>T (p.Gly1096Trp)	LMTK3 (G1096W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2523381	NM_001388485.1(LMTK3):c.3284C>G (p.Thr1095Ser)	LMTK3 (T1095S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119439	NM_001388485.1(LMTK3):c.3178G>A (p.Ala1060Thr)	LMTK3 (A1060T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328953	NM_001388485.1(LMTK3):c.3164C>T (p.Ala1055Val)	LMTK3 (A1055V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2559626	NM_001388485.1(LMTK3):c.3163G>A (p.Ala1055Thr)	LMTK3 (A1055T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119438	NM_001388485.1(LMTK3):c.3161G>C (p.Arg1054Thr)	LMTK3 (R1054T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119436	NM_001388485.1(LMTK3):c.3049A>G (p.Arg1017Gly)	LMTK3 (R1017G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119435	NM_001388485.1(LMTK3):c.2962G>T (p.Val988Leu)	LMTK3 (V988L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258205	NM_001388485.1(LMTK3):c.2953G>A (p.Gly985Arg)	LMTK3 (G985R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302759	NM_001388485.1(LMTK3):c.2906G>A (p.Arg969Lys)	LMTK3 (R969K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2264314	NM_001388485.1(LMTK3):c.2839G>C (p.Gly947Arg)	LMTK3 (G947R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409884	NM_001388485.1(LMTK3):c.2647C>T (p.Arg883Trp)	LMTK3 (R883W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383787	NM_001388485.1(LMTK3):c.2645C>T (p.Ala882Val)	LMTK3 (A882V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598163	NM_001388485.1(LMTK3):c.2592G>A (p.Met864Ile)	LMTK3 (M864I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119434	NM_001388485.1(LMTK3):c.2573G>A (p.Ser858Asn)	LMTK3 (S858N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317313	NM_001388485.1(LMTK3):c.2534C>T (p.Pro845Leu)	LMTK3 (P845L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2229654	NM_001388485.1(LMTK3):c.2486A>C (p.Asp829Ala)	LMTK3 (D829A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2406387	NM_001388485.1(LMTK3):c.2477A>C (p.Glu826Ala)	LMTK3 (E826A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366302	NM_001388485.1(LMTK3):c.2429G>C (p.Gly810Ala)	LMTK3 (G810A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221302	NM_001388485.1(LMTK3):c.2423C>A (p.Pro808Gln)	LMTK3 (P808Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291020	NM_001388485.1(LMTK3):c.2285C>T (p.Ala762Val)	LMTK3 (A762V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119433	NM_001388485.1(LMTK3):c.2261C>T (p.Pro754Leu)	LMTK3 (P754L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119432	NM_001388485.1(LMTK3):c.2261C>G (p.Pro754Arg)	LMTK3 (P754R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2650209	NM_001388485.1(LMTK3):c.2259C>G (p.Pro753=)	LMTK3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2343452	NM_001388485.1(LMTK3):c.2254G>C (p.Ala752Pro)	LMTK3 (A752P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119431	NM_001388485.1(LMTK3):c.2239C>T (p.Arg747Trp)	LMTK3 (R747W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352596	NM_001388485.1(LMTK3):c.2236G>A (p.Gly746Arg)	LMTK3 (G746R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356538	NM_001388485.1(LMTK3):c.2188C>G (p.Pro730Ala)	LMTK3 (P730A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119430	NM_001388485.1(LMTK3):c.2182G>C (p.Ala728Pro)	LMTK3 (A728P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291019	NM_001388485.1(LMTK3):c.2171C>G (p.Pro724Arg)	LMTK3 (P724R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331293	NM_001388485.1(LMTK3):c.2171C>A (p.Pro724His)	LMTK3 (P724H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119429	NM_001388485.1(LMTK3):c.2170C>G (p.Pro724Ala)	LMTK3 (P724A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2485695	NM_001388485.1(LMTK3):c.2168C>G (p.Ala723Gly)	LMTK3 (A723G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525763	NM_001388485.1(LMTK3):c.2141G>A (p.Arg714Gln)	LMTK3 (R714Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2411299	NM_001388485.1(LMTK3):c.2085C>G (p.His695Gln)	LMTK3 (H695Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460624	NM_001388485.1(LMTK3):c.2065G>A (p.Val689Ile)	LMTK3 (V689I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291013	NM_001388485.1(LMTK3):c.2062G>T (p.Ala688Ser)	LMTK3 (A688S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372847	NM_001388485.1(LMTK3):c.2030C>T (p.Ala677Val)	LMTK3 (A677V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119427	NM_001388485.1(LMTK3):c.2023G>A (p.Glu675Lys)	LMTK3 (E675K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517540	NM_001388485.1(LMTK3):c.2009C>G (p.Pro670Arg)	LMTK3 (P670R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119426	NM_001388485.1(LMTK3):c.1981C>A (p.Pro661Thr)	LMTK3 (P661T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291010	NM_001388485.1(LMTK3):c.1835C>T (p.Pro612Leu)	LMTK3 (P612L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355421	NM_001388485.1(LMTK3):c.1825G>A (p.Gly609Ser)	LMTK3 (G609S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371752	NM_001388485.1(LMTK3):c.1762C>A (p.Leu588Ile)	LMTK3 (L588I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2231799	NM_001388485.1(LMTK3):c.1762C>G (p.Leu588Val)	LMTK3 (L588V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2603587	NM_001388485.1(LMTK3):c.1738G>A (p.Val580Met)	LMTK3 (V580M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2600657	NM_001388485.1(LMTK3):c.1674C>A (p.Asp558Glu)	LMTK3 (D558E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291021	NM_001388485.1(LMTK3):c.1625T>G (p.Leu542Trp)	LMTK3 (L542W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2405013	NM_001388485.1(LMTK3):c.1468C>G (p.Arg490Gly)	LMTK3 (R490G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119425	NM_001388485.1(LMTK3):c.1328G>C (p.Arg443Pro)	LMTK3 (R443P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357287	NM_001388485.1(LMTK3):c.1284C>G (p.Asp428Glu)	LMTK3 (D428E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119424	NM_001388485.1(LMTK3):c.1141G>C (p.Ala381Pro)	LMTK3 (A381P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 781513	NM_001388485.1(LMTK3):c.1060C>T (p.Leu354=)	LMTK3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 745041	NM_001388485.1(LMTK3):c.942C>A (p.Leu314=)	LMTK3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 738873	NM_001388485.1(LMTK3):c.646-9C>G	LMTK3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 728999	NM_001388485.1(LMTK3):c.609G>A (p.Thr203=)	LMTK3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3291015	NM_001388485.1(LMTK3):c.561C>G (p.Ser187Arg)	LMTK3 (S187R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291016	NM_001388485.1(LMTK3):c.517C>G (p.Leu173Val)	LMTK3 (L173V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2311405	NM_001388485.1(LMTK3):c.514C>A (p.Pro172Thr)	LMTK3 (P172T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 758160	NM_001388485.1(LMTK3):c.414G>A (p.Glu138=)	LMTK3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3119446	NM_001388485.1(LMTK3):c.397C>G (p.Leu133Val)	LMTK3 (L133V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119437	NM_001388485.1(LMTK3):c.233A>G (p.Glu78Gly)	LMTK3 (E78G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1684576	NM_001388485.1(LMTK3):c.189dup (p.Arg64fs)	LMTK3 (R64fs)	Duplication (frameshift variant)	Intellectual disability +2 more	GUncertain significance
Select item 2535640	NM_001388485.1(LMTK3):c.100C>T (p.Pro34Ser)	LMTK3 (P34S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291011	NM_001388485.1(LMTK3):c.95G>A (p.Arg32Gln)	LMTK3 (R32Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 716791	NM_001388485.1(LMTK3):c.66G>A (p.Pro22=)	LMTK3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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Items: 94