ClinVar for Gene (Select 9064) - ClinVar - NCBI

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

Links from Gene

Items: 1 to 100 of 129

<< First< Prev

Page of 2

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3123014	NM_004672.5(MAP3K6):c.970C>T (p.Arg324Trp)	MAP3K6 (R324W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3123013	NM_004672.5(MAP3K6):c.880A>G (p.Ile294Val)	MAP3K6 (I286V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3123012	NM_004672.5(MAP3K6):c.656G>A (p.Arg219Gln)	MAP3K6 (R211Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3123011	NM_004672.5(MAP3K6):c.556C>T (p.Arg186Trp)	MAP3K6 (R186W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3123010	NM_004672.5(MAP3K6):c.511G>A (p.Val171Ile)	MAP3K6 (V171I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3123009	NM_004672.5(MAP3K6):c.470A>G (p.Gln157Arg)	MAP3K6 (Q157R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3123008	NM_004672.5(MAP3K6):c.3857C>G (p.Ser1286Cys)	MAP3K6 (S1278C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3123007	NM_004672.5(MAP3K6):c.3751T>G (p.Tyr1251Asp)	MAP3K6 (Y1243D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3123006	NM_004672.5(MAP3K6):c.362G>A (p.Ser121Asn)	MAP3K6 (S121N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3123005	NM_004672.5(MAP3K6):c.3623C>T (p.Ala1208Val)	MAP3K6 (A1200V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3123004	NM_004672.5(MAP3K6):c.3589C>G (p.Arg1197Gly)	MAP3K6 (R1197G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3123003	NM_004672.5(MAP3K6):c.3481C>T (p.Pro1161Ser)	MAP3K6 (P1161S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3123001	NM_004672.5(MAP3K6):c.272T>C (p.Leu91Pro)	MAP3K6 (L91P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3123000	NM_004672.5(MAP3K6):c.2689G>A (p.Ala897Thr)	MAP3K6 (A889T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122999	NM_004672.5(MAP3K6):c.2557G>A (p.Gly853Arg)	MAP3K6 (G845R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122998	NM_004672.5(MAP3K6):c.2477A>G (p.Tyr826Cys)	MAP3K6 (Y818C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122997	NM_004672.5(MAP3K6):c.2080A>T (p.Ile694Phe)	MAP3K6 (I694F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122996	NM_004672.5(MAP3K6):c.196G>A (p.Glu66Lys)	MAP3K6 (E66K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122995	NM_004672.5(MAP3K6):c.185G>C (p.Arg62Pro)	MAP3K6 (R62P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122994	NM_004672.5(MAP3K6):c.1753G>C (p.Glu585Gln)	MAP3K6 (E585Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122993	NM_004672.5(MAP3K6):c.16C>G (p.Pro6Ala)	MAP3K6 (P6A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122992	NM_004672.5(MAP3K6):c.1603G>A (p.Val535Met)	MAP3K6 (V535M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122991	NM_004672.5(MAP3K6):c.1100C>T (p.Ser367Leu)	MAP3K6 (S367L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122990	NM_004672.5(MAP3K6):c.1019C>T (p.Pro340Leu)	MAP3K6 (P340L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3059762	NM_004672.5(MAP3K6):c.1364C>T (p.Thr455Ile)	MAP3K6 (T447I +1 more)	Single nucleotide variant (missense variant)	MAP3K6-related disorder	GBenign
Select item 3057500	NM_004672.5(MAP3K6):c.3530G>A (p.Arg1177His)	MAP3K6 (R1169H +1 more)	Single nucleotide variant (missense variant)	MAP3K6-related disorder +1 more	GLikely benign
Select item 3056439	NM_004672.5(MAP3K6):c.2738G>A (p.Arg913His)	MAP3K6 (R905H +1 more)	Single nucleotide variant (missense variant)	MAP3K6-related disorder	GBenign
Select item 3056282	NM_004672.5(MAP3K6):c.2584-6C>T	MAP3K6	Single nucleotide variant (intron variant)	MAP3K6-related disorder	GBenign
Select item 3056146	NM_004672.5(MAP3K6):c.3181G>A (p.Ala1061Thr)	MAP3K6 (A1053T +1 more)	Single nucleotide variant (missense variant)	MAP3K6-related disorder	GLikely benign
Select item 3055994	NM_004672.5(MAP3K6):c.3698G>C (p.Gly1233Ala)	MAP3K6 (G1225A +1 more)	Single nucleotide variant (missense variant)	MAP3K6-related disorder	GBenign
Select item 3055009	NM_004672.5(MAP3K6):c.607G>A (p.Val203Ile)	MAP3K6 (V195I +1 more)	Single nucleotide variant (missense variant)	MAP3K6-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 3053182	NM_004672.5(MAP3K6):c.2751C>T (p.Ser917=)	MAP3K6	Single nucleotide variant (synonymous variant)	MAP3K6-related disorder	GLikely benign
Select item 3050855	NM_004672.5(MAP3K6):c.598G>T (p.Asp200Tyr)	MAP3K6 (D192Y +1 more)	Single nucleotide variant (missense variant)	MAP3K6-related disorder	GLikely benign
Select item 3048868	NM_004672.5(MAP3K6):c.2002C>G (p.Arg668Gly)	MAP3K6 (R660G +1 more)	Single nucleotide variant (missense variant)	MAP3K6-related disorder	GBenign
Select item 3042635	NM_004672.5(MAP3K6):c.1162G>A (p.Val388Ile)	MAP3K6 (V380I +1 more)	Single nucleotide variant (missense variant)	MAP3K6-related disorder	GLikely benign
Select item 3038960	NM_004672.5(MAP3K6):c.318T>C (p.Ala106=)	MAP3K6	Single nucleotide variant (synonymous variant)	MAP3K6-related disorder	GLikely benign
Select item 3038494	NM_004672.5(MAP3K6):c.3070A>G (p.Lys1024Glu)	MAP3K6 (K1016E +1 more)	Single nucleotide variant (missense variant)	MAP3K6-related disorder	GBenign
Select item 3038039	NM_004672.5(MAP3K6):c.1124G>A (p.Arg375Gln)	MAP3K6 (R367Q +1 more)	Single nucleotide variant (missense variant)	MAP3K6-related disorder	GBenign
Select item 3037710	NM_004672.5(MAP3K6):c.1415+9C>T	MAP3K6	Single nucleotide variant (intron variant)	MAP3K6-related disorder	GLikely benign
Select item 3037546	NM_004672.5(MAP3K6):c.3259-10C>T	MAP3K6	Single nucleotide variant (intron variant)	MAP3K6-related disorder	GBenign
Select item 3035484	NM_004672.5(MAP3K6):c.1467C>T (p.Pro489=)	MAP3K6	Single nucleotide variant (synonymous variant)	MAP3K6-related disorder	GLikely benign
Select item 3031754	NM_004672.5(MAP3K6):c.2872C>A (p.Pro958Thr)	MAP3K6 (P950T +1 more)	Single nucleotide variant (missense variant)	MAP3K6-related disorder	GLikely benign
Select item 2664871	GRCh38/hg38 1p36.33-35.1(chr1:99125-34026935)x3	LOC112577491, LOC112577504 +2149 more	Copy number gain	Trisomy 12p	GPathogenic
Select item 2638560	NM_004672.5(MAP3K6):c.738G>A (p.Ala246=)	MAP3K6	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2638559	NM_004672.5(MAP3K6):c.1839C>T (p.Cys613=)	MAP3K6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2638558	NM_004672.5(MAP3K6):c.2837C>T (p.Pro946Leu)	MAP3K6 (P938L +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 2638557	NM_004672.5(MAP3K6):c.3373_3375del (p.Lys1125del)	MAP3K6 (K1117del +1 more)	Deletion (inframe_deletion)	not provided +1 more	GBenign
Select item 2620526	NM_004672.5(MAP3K6):c.2207C>T (p.Ser736Leu)	MAP3K6 (S728L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2616063	NM_004672.5(MAP3K6):c.2876C>T (p.Pro959Leu)	MAP3K6 (P951L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2608033	NM_004672.5(MAP3K6):c.1219C>A (p.Gln407Lys)	MAP3K6 (Q407K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602654	NM_004672.5(MAP3K6):c.2229C>G (p.Asp743Glu)	MAP3K6 (D743E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602168	NM_004672.5(MAP3K6):c.992G>A (p.Arg331Gln)	MAP3K6 (R323Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2575373	NM_004672.5(MAP3K6):c.1352C>T (p.Ala451Val)	MAP3K6 (A443V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2569050	NM_004672.5(MAP3K6):c.1928A>G (p.Tyr643Cys)	MAP3K6 (Y643C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2568660	NM_004672.5(MAP3K6):c.3554G>A (p.Arg1185Gln)	MAP3K6 (R1177Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557195	NM_004672.5(MAP3K6):c.3073C>G (p.Gln1025Glu)	MAP3K6 (Q1017E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555910	NM_004672.5(MAP3K6):c.2504T>G (p.Leu835Arg)	MAP3K6 (L827R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536696	NM_004672.5(MAP3K6):c.2732G>T (p.Arg911Met)	MAP3K6 (R911M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532144	NM_004672.5(MAP3K6):c.2216G>A (p.Gly739Glu)	MAP3K6 (G731E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519177	NM_004672.5(MAP3K6):c.1667T>C (p.Leu556Pro)	MAP3K6 (L556P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517456	NM_004672.5(MAP3K6):c.289G>A (p.Gly97Arg)	MAP3K6 (G97R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2480589	NM_004672.5(MAP3K6):c.2675G>A (p.Arg892His)	MAP3K6 (R892H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2475199	NM_004672.5(MAP3K6):c.2613G>A (p.Met871Ile)	MAP3K6 (M871I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470582	NM_004672.5(MAP3K6):c.3782G>A (p.Arg1261His)	MAP3K6 (R1261H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466727	NM_004672.5(MAP3K6):c.739C>T (p.Arg247Trp)	MAP3K6 (R239W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464423	NM_004672.5(MAP3K6):c.803G>A (p.Ser268Asn)	MAP3K6 (S268N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464387	NM_004672.5(MAP3K6):c.767G>A (p.Arg256Gln)	MAP3K6 (R248Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462094	NM_004672.5(MAP3K6):c.233C>T (p.Ala78Val)	MAP3K6 (A78V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461489	NM_004672.5(MAP3K6):c.1868C>T (p.Pro623Leu)	MAP3K6 (P615L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454282	NM_004672.5(MAP3K6):c.790C>T (p.Arg264Trp)	MAP3K6 (R256W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410228	NM_004672.5(MAP3K6):c.2767C>T (p.Arg923Trp)	MAP3K6 (R923W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410061	NM_004672.5(MAP3K6):c.718C>T (p.Arg240Trp)	MAP3K6 (R240W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409225	NM_004672.5(MAP3K6):c.3691G>C (p.Asp1231His)	MAP3K6 (D1223H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402911	NM_004672.5(MAP3K6):c.1463G>A (p.Arg488Lys)	MAP3K6 (R480K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401011	NM_004672.5(MAP3K6):c.1294G>A (p.Val432Met)	MAP3K6 (V424M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378716	NM_004672.5(MAP3K6):c.2894A>G (p.Tyr965Cys)	MAP3K6 (Y965C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375569	NM_004672.5(MAP3K6):c.2881C>A (p.Arg961Ser)	MAP3K6 (R961S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368512	NM_004672.5(MAP3K6):c.2470C>T (p.Arg824Cys)	MAP3K6 (R816C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356802	NM_004672.5(MAP3K6):c.331T>C (p.Tyr111His)	MAP3K6 (Y111H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355463	NM_004672.5(MAP3K6):c.3655C>G (p.Gln1219Glu)	MAP3K6 (Q1211E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345359	NM_004672.5(MAP3K6):c.1630C>T (p.Arg544Trp)	MAP3K6 (R536W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333776	NM_004672.5(MAP3K6):c.218G>A (p.Arg73His)	MAP3K6 (R73H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331121	NM_004672.5(MAP3K6):c.1763G>A (p.Cys588Tyr)	MAP3K6 (C580Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322684	NM_004672.5(MAP3K6):c.187G>A (p.Glu63Lys)	MAP3K6 (E63K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315833	NM_004672.5(MAP3K6):c.1064T>C (p.Met355Thr)	MAP3K6 (M355T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309698	NM_004672.5(MAP3K6):c.964C>G (p.Leu322Val)	MAP3K6 (L314V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309281	NM_004672.5(MAP3K6):c.257G>A (p.Arg86Gln)	MAP3K6 (R86Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2307469	NM_004672.5(MAP3K6):c.188A>G (p.Glu63Gly)	MAP3K6 (E63G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290484	NM_004672.5(MAP3K6):c.2165T>C (p.Met722Thr)	MAP3K6 (M714T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287788	NM_004672.5(MAP3K6):c.2917G>A (p.Val973Met)	MAP3K6 (V965M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275777	NM_004672.5(MAP3K6):c.578G>A (p.Gly193Asp)	MAP3K6 (G193D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2267578	NM_004672.5(MAP3K6):c.1824C>G (p.His608Gln)	MAP3K6 (H608Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2265130	NM_004672.5(MAP3K6):c.1624G>A (p.Glu542Lys)	MAP3K6 (E534K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2264878	NM_004672.5(MAP3K6):c.3029A>G (p.Gln1010Arg)	MAP3K6 (Q1002R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2264675	NM_004672.5(MAP3K6):c.545C>T (p.Thr182Met)	MAP3K6 (T174M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262351	NM_004672.5(MAP3K6):c.22T>G (p.Ser8Ala)	MAP3K6 (S8A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262105	NM_004672.5(MAP3K6):c.1216G>T (p.Gly406Trp)	MAP3K6 (G398W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257858	NM_004672.5(MAP3K6):c.3779C>T (p.Thr1260Ile)	MAP3K6 (T1260I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251543	NM_004672.5(MAP3K6):c.1339G>T (p.Ala447Ser)	MAP3K6 (A447S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248706	NM_004672.5(MAP3K6):c.721C>T (p.Arg241Trp)	MAP3K6 (R241W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

<< First< Prev

Page of 2