Map3k8 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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215 records found for search term Map3k8

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
151712950	CV1479718	single nucleotide variant	NM_005204.4(MAP3K8):c.336+4C>T	not provided [RCV001889754]	uncertain significance	10	30439278	30439278	Human		name
156026305	CV1906603	single nucleotide variant	NM_005204.4(MAP3K8):c.766+6T>C	not provided [RCV003100442]	uncertain significance	10	30450525	30450525	Human		name
156393990	CV1962574	single nucleotide variant	NM_005204.4(MAP3K8):c.505-6T>C	not provided [RCV002584166]	likely benign	10	30450252	30450252	Human		name
156108789	CV1988592	single nucleotide variant	NM_005204.4(MAP3K8):c.336+7T>G	not provided [RCV002622491]	likely benign	10	30439281	30439281	Human		name
156061253	CV2008274	single nucleotide variant	NM_005204.4(MAP3K8):c.874-9C>G	not provided [RCV002705394]	likely benign	10	30458075	30458075	Human		name
156106573	CV2061866	single nucleotide variant	NM_005204.4(MAP3K8):c.504+6T>C	not provided [RCV002824753]	uncertain significance	10	30447955	30447955	Human		name
405239901	CV2989913	single nucleotide variant	NM_005204.4(MAP3K8):c.336+5G>A	not provided [RCV003683835]	uncertain significance	10	30439279	30439279	Human		name
405191316	CV3069953	single nucleotide variant	NM_005204.4(MAP3K8):c.337-6T>C	not provided [RCV003729744]	likely benign	10	30447776	30447776	Human		name
405225646	CV3142397	single nucleotide variant	NM_005204.4(MAP3K8):c.873+9G>A	not provided [RCV003847936]	likely benign	10	30451753	30451753	Human		name
597917762	CV3789621	single nucleotide variant	NM_005204.4(MAP3K8):c.767-8C>A	not provided [RCV005129716]	likely benign	10	30451630	30451630	Human		name
597961822	CV3840847	single nucleotide variant	NM_005204.4(MAP3K8):c.505-7G>A	not provided [RCV005193140]	likely benign	10	30450251	30450251	Human		name
150495197	CV1266187	single nucleotide variant	NM_005204.4(MAP3K8):c.336+47A>G	not provided [RCV001688509]	benign	10	30439321	30439321	Human		name
152169633	CV1529294	single nucleotide variant	NM_005204.4(MAP3K8):c.336+14C>T	not provided [RCV002161508]	likely benign	10	30439288	30439288	Human		name
152082548	CV1548470	single nucleotide variant	NM_005204.4(MAP3K8):c.336+19A>T	not provided [RCV002076564]	benign	10	30439293	30439293	Human		name
152090140	CV1563229	single nucleotide variant	NM_005204.4(MAP3K8):c.505-10T>C	MAP3K8-related disorder [RCV003971019]\|not provided [RCV002113964]	likely benign	10	30450248	30450248	Human	1	name , trait , alternate_id
152075708	CV1653041	single nucleotide variant	NM_005204.4(MAP3K8):c.874-11T>A	not provided [RCV002148668]	likely benign	10	30458073	30458073	Human		name
156376541	CV1896079	single nucleotide variant	NM_005204.4(MAP3K8):c.1273+8C>T	not provided [RCV003092921]	likely benign	10	30459509	30459509	Human		name
156122850	CV1969264	single nucleotide variant	NM_005204.4(MAP3K8):c.336+15G>A	not provided [RCV002593196]	likely benign	10	30439289	30439289	Human		name
156257056	CV1977377	single nucleotide variant	NM_005204.4(MAP3K8):c.336+20G>A	not provided [RCV002597657]	likely benign	10	30439294	30439294	Human		name
156005389	CV2179437	single nucleotide variant	NM_005204.4(MAP3K8):c.336+15G>T	not provided [RCV003034968]	likely benign	10	30439289	30439289	Human		name
405199330	CV3164474	single nucleotide variant	NM_005204.4(MAP3K8):c.873+15A>G	not provided [RCV003860531]	likely benign	10	30451759	30451759	Human		name
405228965	CV3180463	single nucleotide variant	NM_005204.4(MAP3K8):c.873+14C>T	not provided [RCV003864884]	likely benign	10	30451758	30451758	Human		name
597937767	CV3852674	single nucleotide variant	NM_005204.4(MAP3K8):c.874-19T>C	not provided [RCV005187073]	likely benign	10	30458065	30458065	Human		name
597878989	CV3856900	single nucleotide variant	NM_005204.4(MAP3K8):c.874-14C>T	not provided [RCV005198700]	likely benign	10	30458070	30458070	Human		name
150333094	CV1169399	single nucleotide variant	NM_005204.4(MAP3K8):c.336+286C>T	not provided [RCV001537158]	benign	10	30439560	30439560	Human		name
150331532	CV1169400	single nucleotide variant	NM_005204.4(MAP3K8):c.505-129A>G	not provided [RCV001536513]	benign	10	30450129	30450129	Human		name
150514320	CV1213426	single nucleotide variant	NM_005204.4(MAP3K8):c.336+261T>C	not provided [RCV001599017]	benign	10	30439535	30439535	Human		name
150448012	CV1216203	single nucleotide variant	NM_005204.4(MAP3K8):c.1274-44G>T	not provided [RCV001611501]	benign	10	30460662	30460662	Human		name
150465308	CV1252860	single nucleotide variant	NM_005204.4(MAP3K8):c.1273+68T>C	not provided [RCV001670184]	benign	10	30459569	30459569	Human		name
150447464	CV1253409	single nucleotide variant	NM_005204.4(MAP3K8):c.767-188G>A	not provided [RCV001667337]	benign	10	30451450	30451450	Human		name
150480343	CV1258416	duplication	NM_005204.4(MAP3K8):c.1026+41dup	not provided [RCV001685835]	benign	10	30458268	30458269	Human		name
150440138	CV1287140	single nucleotide variant	NM_005204.4(MAP3K8):c.874-189C>T	not provided [RCV001725055]	benign	10	30457895	30457895	Human		name
152136821	CV1528534	single nucleotide variant	NM_005204.4(MAP3K8):c.1273+12C>T	not provided [RCV002100229]	benign	10	30459513	30459513	Human		name
152097384	CV1534238	single nucleotide variant	NM_005204.4(MAP3K8):c.1273+10C>T	not provided [RCV002095033]	likely benign	10	30459511	30459511	Human		name
152114800	CV1537411	single nucleotide variant	NM_005204.4(MAP3K8):c.1026+16C>T	not provided [RCV002134958]	benign	10	30458252	30458252	Human		name
152030070	CV1568857	single nucleotide variant	NM_005204.4(MAP3K8):c.1026+15A>G	not provided [RCV002186363]	likely benign	10	30458251	30458251	Human		name
155949218	CV2087971	single nucleotide variant	NM_005204.4(MAP3K8):c.1273+14G>A	not provided [RCV002880403]	likely benign	10	30459515	30459515	Human		name
156127801	CV2100673	single nucleotide variant	NM_005204.4(MAP3K8):c.1027-13G>A	not provided [RCV002889823]	likely benign	10	30459242	30459242	Human		name
405096098	CV2944098	single nucleotide variant	NM_005204.4(MAP3K8):c.1274-20T>C	not provided [RCV003665659]	likely benign	10	30460686	30460686	Human		name
597973653	CV3820633	single nucleotide variant	NM_005204.4(MAP3K8):c.1274-19G>T	not provided [RCV005168150]	likely benign	10	30460687	30460687	Human		name
597884800	CV3834994	single nucleotide variant	NM_005204.4(MAP3K8):c.1274-17A>T	not provided [RCV005178718]	likely benign	10	30460689	30460689	Human		name
150472815	CV1281289	duplication	NM_005204.4(MAP3K8):c.1273+170dup	not provided [RCV001713429]	benign	10	30459660	30459661	Human		name
152050009	CV1615234	single nucleotide variant	NM_005204.4(MAP3K8):c.9C>T (p.Tyr3=)	not provided [RCV002089034]	likely benign	10	30438947	30438947	Human		name
152082319	CV1608002	single nucleotide variant	NM_005204.4(MAP3K8):c.69G>A (p.Val23=)	not provided [RCV002193183]	likely benign	10	30439007	30439007	Human		name
156279157	CV2005122	single nucleotide variant	NM_005204.4(MAP3K8):c.93A>G (p.Glu31=)	not provided [RCV002646783]	likely benign	10	30439031	30439031	Human		name
155946330	CV2072661	single nucleotide variant	NM_005204.4(MAP3K8):c.5A>C (p.Glu2Ala)	not provided [RCV002862088]	uncertain significance	10	30438943	30438943	Human		name
402479842	CV3170615	single nucleotide variant	NM_005204.4(MAP3K8):c.42T>C (p.Ile14=)	not provided [RCV003875817]	likely benign	10	30438980	30438980	Human		name
150330406	CV1164353	single nucleotide variant	NM_005204.4(MAP3K8):c.234T>C (p.Tyr78=)	not provided [RCV001537203]\|not specified [RCV001528717]	benign	10	30439172	30439172	Human	4	name
151735127	CV1391131	single nucleotide variant	NM_005204.4(MAP3K8):c.20G>A (p.Gly7Glu)	not provided [RCV002005205]	uncertain significance	10	30438958	30438958	Human		name
152175749	CV1527152	single nucleotide variant	NM_005204.4(MAP3K8):c.243G>A (p.Val81=)	not provided [RCV002163886]	likely benign	10	30439181	30439181	Human		name
152076947	CV1592060	single nucleotide variant	NM_005204.4(MAP3K8):c.222A>C (p.Ser74=)	MAP3K8-related disorder [RCV003951027]\|not provided [RCV002112234]	benign\|likely benign	10	30439160	30439160	Human	1	name , trait , alternate_id
156052915	CV2027450	single nucleotide variant	NM_005204.4(MAP3K8):c.138A>G (p.Leu46=)	not provided [RCV002736570]	likely benign	10	30439076	30439076	Human		name
156224205	CV2081017	single nucleotide variant	NM_005204.4(MAP3K8):c.240T>C (p.Thr80=)	not provided [RCV002853326]	likely benign	10	30439178	30439178	Human		name
329361094	CV2463274	single nucleotide variant	NM_005204.4(MAP3K8):c.26A>G (p.Asp9Gly)	not specified [RCV004275037]	uncertain significance	10	30438964	30438964	Human		name
405178191	CV3056482	single nucleotide variant	NM_005204.4(MAP3K8):c.174G>A (p.Glu58=)	not provided [RCV003728531]	likely benign	10	30439112	30439112	Human		name
405206021	CV3068300	single nucleotide variant	NM_005204.4(MAP3K8):c.15C>A (p.Ser5Arg)	not provided [RCV003731319]	uncertain significance	10	30438953	30438953	Human		name
405187758	CV3149196	single nucleotide variant	NM_005204.4(MAP3K8):c.222A>G (p.Ser74=)	not provided [RCV003843122]	likely benign	10	30439160	30439160	Human		name
405811277	CV3284866	single nucleotide variant	NM_005204.4(MAP3K8):c.14G>T (p.Ser5Ile)	not provided [RCV005104532]\|not specified [RCV004408402]	uncertain significance	10	30438952	30438952	Human		name
597867623	CV3739075	single nucleotide variant	NM_005204.4(MAP3K8):c.10A>C (p.Met4Leu)	not provided [RCV005068142]	uncertain significance	10	30438948	30438948	Human		name
597951725	CV3798406	single nucleotide variant	NM_005204.4(MAP3K8):c.187C>T (p.Leu63=)	not provided [RCV005136187]	likely benign	10	30439125	30439125	Human		name
15198634	CV701314	single nucleotide variant	NM_005204.4(MAP3K8):c.159T>C (p.Ser53=)	not provided [RCV000956815]	benign	10	30439097	30439097	Human		name
150505362	CV1286169	duplication	NM_005204.4(MAP3K8):c.1026+40_1026+41dup	not provided [RCV001719594]	benign	10	30458268	30458269	Human		name
151864887	CV1370882	single nucleotide variant	NM_005204.4(MAP3K8):c.630C>T (p.Gly210=)	not provided [RCV001884412]	uncertain significance	10	30450383	30450383	Human		name
151777155	CV1381083	single nucleotide variant	NM_005204.4(MAP3K8):c.71C>T (p.Ser24Phe)	not provided [RCV002045795]	uncertain significance	10	30439009	30439009	Human		name
152142806	CV1533253	single nucleotide variant	NM_005204.4(MAP3K8):c.660G>A (p.Glu220=)	not provided [RCV002156989]	likely benign	10	30450413	30450413	Human		name
152095359	CV1575193	single nucleotide variant	NM_005204.4(MAP3K8):c.375C>T (p.Ser125=)	MAP3K8-related disorder [RCV003951192]\|not provided [RCV002132553]	likely benign	10	30447820	30447820	Human	1	name , trait , alternate_id
152154876	CV1579547	single nucleotide variant	NM_005204.4(MAP3K8):c.834C>T (p.Thr278=)	not provided [RCV002158716]	likely benign	10	30451705	30451705	Human		name
152082000	CV1589503	single nucleotide variant	NM_005204.4(MAP3K8):c.573A>G (p.Ala191=)	not provided [RCV002112879]	likely benign	10	30450326	30450326	Human		name
152100145	CV1595696	single nucleotide variant	NM_005204.4(MAP3K8):c.465A>G (p.Ala155=)	not provided [RCV002213895]	likely benign	10	30447910	30447910	Human		name
152064356	CV1612263	single nucleotide variant	NM_005204.4(MAP3K8):c.858C>T (p.Asp286=)	MAP3K8-related disorder [RCV003958868]\|not provided [RCV002128761]	likely benign	10	30451729	30451729	Human	1	name , trait , alternate_id
152051897	CV1622502	single nucleotide variant	NM_005204.4(MAP3K8):c.480G>A (p.Thr160=)	not provided [RCV002207626]	likely benign	10	30447925	30447925	Human		name
152151596	CV1626505	single nucleotide variant	NM_005204.4(MAP3K8):c.384C>G (p.Leu128=)	not provided [RCV002202054]	likely benign	10	30447829	30447829	Human		name
152070509	CV1628411	single nucleotide variant	NM_005204.4(MAP3K8):c.570C>T (p.Ile190=)	not provided [RCV002169226]	likely benign	10	30450323	30450323	Human		name
152032337	CV1629381	single nucleotide variant	NM_005204.4(MAP3K8):c.495G>A (p.Ala165=)	not provided [RCV002106344]	likely benign	10	30447940	30447940	Human		name
152055282	CV1637342	single nucleotide variant	NM_005204.4(MAP3K8):c.441C>T (p.Gly147=)	not provided [RCV002208006]	likely benign	10	30447886	30447886	Human		name
152098210	CV1650309	single nucleotide variant	NM_005204.4(MAP3K8):c.669A>G (p.Gly223=)	not provided [RCV002114981]	likely benign	10	30450422	30450422	Human		name
152099394	CV1650493	single nucleotide variant	NM_005204.4(MAP3K8):c.966G>A (p.Thr322=)	not provided [RCV002115122]	likely benign	10	30458176	30458176	Human		name
156440675	CV1943736	single nucleotide variant	NM_005204.4(MAP3K8):c.969C>T (p.Gly323=)	MAP3K8-related disorder [RCV004754963]\|not provided [RCV003110712]	likely benign	10	30458179	30458179	Human	1	name , trait , alternate_id
156447427	CV1945380	single nucleotide variant	NM_005204.4(MAP3K8):c.585C>T (p.Gly195=)	MAP3K8-related disorder [RCV003928950]\|not provided [RCV003118955]	likely benign	10	30450338	30450338	Human	1	name , trait , alternate_id
156444835	CV1948879	single nucleotide variant	NM_005204.4(MAP3K8):c.82G>A (p.Asp28Asn)	not provided [RCV003115765]	uncertain significance	10	30439020	30439020	Human		name
156301755	CV1955610	single nucleotide variant	NM_005204.4(MAP3K8):c.909C>G (p.Gly303=)	not provided [RCV002578257]	likely benign	10	30458119	30458119	Human		name
156411342	CV1977138	single nucleotide variant	NM_005204.4(MAP3K8):c.615C>G (p.Leu205=)	not provided [RCV002608226]	likely benign	10	30450368	30450368	Human		name
156010420	CV1991804	single nucleotide variant	NM_005204.4(MAP3K8):c.777T>C (p.Ile259=)	not provided [RCV002618875]	likely benign	10	30451648	30451648	Human		name
156361986	CV2003260	single nucleotide variant	NM_005204.4(MAP3K8):c.366A>G (p.Gln122=)	not provided [RCV002676308]	likely benign	10	30447811	30447811	Human		name
156375224	CV2003995	single nucleotide variant	NM_005204.4(MAP3K8):c.945C>T (p.Ala315=)	not provided [RCV002653240]	likely benign	10	30458155	30458155	Human		name
156290369	CV2060264	single nucleotide variant	NM_005204.4(MAP3K8):c.351A>G (p.Gln117=)	not provided [RCV002807320]	likely benign	10	30447796	30447796	Human		name
156155275	CV2098691	single nucleotide variant	NM_005204.4(MAP3K8):c.525G>A (p.Lys175=)	not provided [RCV002890791]	likely benign	10	30450278	30450278	Human		name
405117902	CV3020268	single nucleotide variant	NM_005204.4(MAP3K8):c.348C>A (p.Pro116=)	not provided [RCV003700341]	likely benign	10	30447793	30447793	Human		name
405179567	CV3027566	single nucleotide variant	NM_005204.4(MAP3K8):c.519A>G (p.Gln173=)	not provided [RCV003705306]	likely benign	10	30450272	30450272	Human		name
405060718	CV3129522	single nucleotide variant	NM_005204.4(MAP3K8):c.807G>A (p.Val269=)	not provided [RCV003832791]	likely benign	10	30451678	30451678	Human		name
405212132	CV3142625	single nucleotide variant	NM_005204.4(MAP3K8):c.64A>C (p.Asn22His)	not provided [RCV003845982]	uncertain significance	10	30439002	30439002	Human		name
405289828	CV3219022	single nucleotide variant	NM_005204.4(MAP3K8):c.906G>A (p.Arg302=)	MAP3K8-related disorder [RCV003962032]	likely benign	10	30458116	30458116	Human		name , trait , alternate_id
597891335	CV3749369	single nucleotide variant	NM_005204.4(MAP3K8):c.655C>T (p.Leu219=)	not provided [RCV005071153]	likely benign	10	30450408	30450408	Human		name
597933946	CV3750370	single nucleotide variant	NM_005204.4(MAP3K8):c.885C>T (p.Ser295=)	not provided [RCV005076295]	likely benign	10	30458095	30458095	Human		name
597961926	CV3753559	single nucleotide variant	NM_005204.4(MAP3K8):c.573A>T (p.Ala191=)	not provided [RCV005081863]	likely benign	10	30450326	30450326	Human		name
597893011	CV3763412	single nucleotide variant	NM_005204.4(MAP3K8):c.417T>C (p.Ile139=)	not provided [RCV005110992]	likely benign	10	30447862	30447862	Human		name
597966118	CV3793913	single nucleotide variant	NM_005204.4(MAP3K8):c.510A>G (p.Pro170=)	not provided [RCV005140295]	likely benign	10	30450263	30450263	Human		name
597953327	CV3815993	single nucleotide variant	NM_005204.4(MAP3K8):c.507C>T (p.Ile169=)	not provided [RCV005161745]	likely benign	10	30450260	30450260	Human		name
597942574	CV3847283	single nucleotide variant	NM_005204.4(MAP3K8):c.951C>T (p.Leu317=)	not provided [RCV005188203]	likely benign	10	30458161	30458161	Human		name
597862496	CV3860553	single nucleotide variant	NM_005204.4(MAP3K8):c.942G>A (p.Gly314=)	not provided [RCV005196081]	likely benign	10	30458152	30458152	Human		name
15202363	CV701315	single nucleotide variant	NM_005204.4(MAP3K8):c.948G>A (p.Thr316=)	MAP3K8-related disorder [RCV003926071]\|not provided [RCV000957892]	benign	10	30458158	30458158	Human	1	name , trait , alternate_id
15169259	CV712332	single nucleotide variant	NM_005204.4(MAP3K8):c.915A>T (p.Ser305=)	not provided [RCV000971776]	benign	10	30458125	30458125	Human		name
15172035	CV767705	single nucleotide variant	NM_005204.4(MAP3K8):c.360T>C (p.Arg120=)	not provided [RCV000928028]	likely benign	10	30447805	30447805	Human		name
151843657	CV1375680	single nucleotide variant	NM_005204.4(MAP3K8):c.196A>G (p.Ser66Gly)	not provided [RCV001995061]	uncertain significance	10	30439134	30439134	Human		name
151752385	CV1379706	single nucleotide variant	NM_005204.4(MAP3K8):c.1314C>T (p.Leu438=)	not provided [RCV001948273]	likely benign	10	30460746	30460746	Human		name
151708763	CV1383750	single nucleotide variant	NM_005204.4(MAP3K8):c.1347C>T (p.Gly449=)	not provided [RCV001907530]	likely benign	10	30460779	30460779	Human		name
151881271	CV1395801	single nucleotide variant	NM_005204.4(MAP3K8):c.146T>A (p.Met49Lys)	not provided [RCV002036917]\|not specified [RCV005370148]	uncertain significance	10	30439084	30439084	Human		name
151775445	CV1402576	single nucleotide variant	NM_005204.4(MAP3K8):c.277A>G (p.Asn93Asp)	not provided [RCV001929934]	uncertain significance	10	30439215	30439215	Human		name
151817592	CV1427454	single nucleotide variant	NM_005204.4(MAP3K8):c.169G>A (p.Asp57Asn)	MAP3K8-related disorder [RCV004754795]\|not provided [RCV001878901]\|not specified [RCV004040517]	uncertain significance	10	30439107	30439107	Human	1	name , trait , alternate_id
151848969	CV1431127	single nucleotide variant	NM_005204.4(MAP3K8):c.1338C>A (p.Ile446=)	not provided [RCV001922510]	likely benign\|uncertain significance	10	30460770	30460770	Human		name
151868763	CV1438149	single nucleotide variant	NM_005204.4(MAP3K8):c.176G>A (p.Arg59His)	not provided [RCV001906201]	uncertain significance	10	30439114	30439114	Human		name
151836423	CV1473016	single nucleotide variant	NM_005204.4(MAP3K8):c.141G>A (p.Met47Ile)	not provided [RCV002051259]\|not specified [RCV004935217]	uncertain significance	10	30439079	30439079	Human		name
151870987	CV1488671	single nucleotide variant	NM_005204.4(MAP3K8):c.268C>T (p.His90Tyr)	not provided [RCV002035663]	uncertain significance	10	30439206	30439206	Human		name
152133130	CV1545274	single nucleotide variant	NM_005204.4(MAP3K8):c.175C>T (p.Arg59Cys)	not provided [RCV002119341]	likely benign	10	30439113	30439113	Human		name
152163320	CV1618979	single nucleotide variant	NM_005204.4(MAP3K8):c.1098A>G (p.Glu366=)	not provided [RCV002123587]	likely benign	10	30459326	30459326	Human		name
152132328	CV1621363	single nucleotide variant	NM_005204.4(MAP3K8):c.1170G>A (p.Pro390=)	not provided [RCV002218242]	likely benign	10	30459398	30459398	Human		name
152111110	CV1626104	single nucleotide variant	NM_005204.4(MAP3K8):c.1269T>C (p.Ile423=)	not provided [RCV002153065]	benign	10	30459497	30459497	Human		name
152108105	CV1634762	single nucleotide variant	NM_005204.4(MAP3K8):c.1110G>A (p.Glu370=)	not provided [RCV002079878]	likely benign	10	30459338	30459338	Human		name
152028287	CV1642727	single nucleotide variant	NM_005204.4(MAP3K8):c.1296C>T (p.Thr432=)	not provided [RCV002185785]	likely benign	10	30460728	30460728	Human		name
152163076	CV1648124	single nucleotide variant	NM_005204.4(MAP3K8):c.1174A>C (p.Arg392=)	not provided [RCV002123548]	likely benign	10	30459402	30459402	Human		name
152034575	CV1666108	single nucleotide variant	NM_005204.4(MAP3K8):c.1056C>T (p.Asp352=)	MAP3K8-related disorder [RCV004754833]\|not provided [RCV002106770]	benign\|likely benign	10	30459284	30459284	Human	1	name , trait , alternate_id
156393573	CV1876175	single nucleotide variant	NM_005204.4(MAP3K8):c.1020G>A (p.Leu340=)	not provided [RCV003068310]	likely benign	10	30458230	30458230	Human		name
156374614	CV1917403	single nucleotide variant	NM_005204.4(MAP3K8):c.1200T>C (p.Ser400=)	not provided [RCV002603477]	likely benign	10	30459428	30459428	Human		name
156003756	CV1988008	single nucleotide variant	NM_005204.4(MAP3K8):c.269A>G (p.His90Arg)	not provided [RCV002618569]	uncertain significance	10	30439207	30439207	Human		name
156253524	CV2041163	single nucleotide variant	NM_005204.4(MAP3K8):c.1281G>C (p.Ser427=)	not provided [RCV002806091]	likely benign	10	30460713	30460713	Human		name
156373794	CV2052771	single nucleotide variant	NM_005204.4(MAP3K8):c.1281G>A (p.Ser427=)	not provided [RCV002814517]	likely benign	10	30460713	30460713	Human		name
156159790	CV2147271	single nucleotide variant	NM_005204.4(MAP3K8):c.227T>C (p.Val76Ala)	not provided [RCV003023151]	uncertain significance	10	30439165	30439165	Human		name
156211624	CV2170901	single nucleotide variant	NM_005204.4(MAP3K8):c.155A>G (p.Asp52Gly)	not provided [RCV003042353]	uncertain significance	10	30439093	30439093	Human		name
155971535	CV2227878	single nucleotide variant	NM_005204.4(MAP3K8):c.160A>G (p.Asn54Asp)	not specified [RCV004094515]	uncertain significance	10	30439098	30439098	Human		name
401742296	CV2718758	single nucleotide variant	NM_005204.4(MAP3K8):c.103G>T (p.Ala35Ser)	not specified [RCV004328511]	uncertain significance	10	30439041	30439041	Human		name
405210805	CV2966841	single nucleotide variant	NM_005204.4(MAP3K8):c.200G>A (p.Gly67Asp)	not provided [RCV003679365]\|not specified [RCV004371622]	uncertain significance	10	30439138	30439138	Human		name
405064014	CV3020588	single nucleotide variant	NM_005204.4(MAP3K8):c.1266C>T (p.Asn422=)	not provided [RCV003697816]	likely benign	10	30459494	30459494	Human		name
405039169	CV3067810	single nucleotide variant	NM_005204.4(MAP3K8):c.1389G>A (p.Thr463=)	not provided [RCV003739779]	likely benign	10	30460821	30460821	Human		name
404999004	CV3120129	single nucleotide variant	NM_005204.4(MAP3K8):c.1296C>G (p.Thr432=)	not provided [RCV003827919]	likely benign	10	30460728	30460728	Human		name
405187358	CV3149155	single nucleotide variant	NM_005204.4(MAP3K8):c.1020G>T (p.Leu340=)	not provided [RCV003843081]	likely benign	10	30458230	30458230	Human		name
596945661	CV3547984	single nucleotide variant	NM_005204.4(MAP3K8):c.1299G>A (p.Glu433=)	not provided [RCV004809315]	likely benign	10	30460731	30460731	Human		name
597873767	CV3747378	single nucleotide variant	NM_005204.4(MAP3K8):c.230G>T (p.Arg77Ile)	not provided [RCV005069062]	uncertain significance	10	30439168	30439168	Human		name
597897555	CV3834740	single nucleotide variant	NM_005204.4(MAP3K8):c.1395A>G (p.Glu465=)	not provided [RCV005180651]	uncertain significance	10	30460827	30460827	Human		name
15198637	CV701316	single nucleotide variant	NM_005204.4(MAP3K8):c.1344C>T (p.Leu448=)	not provided [RCV000956816]	benign	10	30460776	30460776	Human		name
15133485	CV752076	single nucleotide variant	NM_005204.4(MAP3K8):c.1362C>T (p.Tyr454=)	not provided [RCV000920523]	likely benign	10	30460794	30460794	Human		name
151852417	CV1349029	single nucleotide variant	NM_005204.4(MAP3K8):c.587C>T (p.Ala196Val)	not provided [RCV001922974]	uncertain significance	10	30450340	30450340	Human		name
151789456	CV1388980	single nucleotide variant	NM_005204.4(MAP3K8):c.418G>T (p.Gly140Cys)	not provided [RCV002010550]	uncertain significance	10	30447863	30447863	Human		name
151793088	CV1411284	single nucleotide variant	NM_005204.4(MAP3K8):c.595T>A (p.Trp199Arg)	not provided [RCV002010883]	uncertain significance	10	30450348	30450348	Human		name
151729358	CV1416513	single nucleotide variant	NM_005204.4(MAP3K8):c.557G>A (p.Arg186Gln)	not provided [RCV002004610]	uncertain significance	10	30450310	30450310	Human		name
151819963	CV1450132	single nucleotide variant	NM_005204.4(MAP3K8):c.947C>T (p.Thr316Met)	not provided [RCV001879120]	uncertain significance	10	30458157	30458157	Human		name
151838271	CV1492676	single nucleotide variant	NM_005204.4(MAP3K8):c.382C>T (p.Leu128Phe)	not provided [RCV001881038]	uncertain significance	10	30447827	30447827	Human		name
151865998	CV1495244	single nucleotide variant	NM_005204.4(MAP3K8):c.946A>G (p.Thr316Ala)	not provided [RCV001980723]	uncertain significance	10	30458156	30458156	Human		name
151812744	CV1498162	single nucleotide variant	NM_005204.4(MAP3K8):c.562G>A (p.Glu188Lys)	not provided [RCV001953990]	uncertain significance	10	30450315	30450315	Human		name
156448465	CV1950747	single nucleotide variant	NM_005204.4(MAP3K8):c.334A>G (p.Met112Val)	not provided [RCV003120027]	uncertain significance	10	30439272	30439272	Human		name
156312593	CV1969829	single nucleotide variant	NM_005204.4(MAP3K8):c.835G>A (p.Glu279Lys)	not provided [RCV002578775]	uncertain significance	10	30451706	30451706	Human		name
156416777	CV1969998	single nucleotide variant	NM_005204.4(MAP3K8):c.304C>G (p.Arg102Gly)	not provided [RCV002589870]	uncertain significance	10	30439242	30439242	Human		name
155989688	CV1990430	single nucleotide variant	NM_005204.4(MAP3K8):c.473T>C (p.Ile158Thr)	not provided [RCV002617967]	uncertain significance	10	30447918	30447918	Human		name
155971329	CV2079237	single nucleotide variant	NM_005204.4(MAP3K8):c.479C>T (p.Thr160Met)	not provided [RCV002881501]	uncertain significance	10	30447924	30447924	Human		name
156014937	CV2086953	single nucleotide variant	NM_005204.4(MAP3K8):c.687A>T (p.Glu229Asp)	not provided [RCV002866305]	uncertain significance	10	30450440	30450440	Human		name
401738795	CV2708161	single nucleotide variant	NM_005204.4(MAP3K8):c.530C>G (p.Ser177Cys)	not specified [RCV004311528]	uncertain significance	10	30450283	30450283	Human		name
401922967	CV2796661	single nucleotide variant	NM_005204.4(MAP3K8):c.346C>A (p.Pro116Thr)	MAP3K8-related disorder [RCV003404280]	uncertain significance	10	30447791	30447791	Human		name , trait , alternate_id
405093109	CV2878112	single nucleotide variant	NM_005204.4(MAP3K8):c.998G>A (p.Arg333His)	not provided [RCV003549955]	uncertain significance	10	30458208	30458208	Human		name
402470901	CV2908037	single nucleotide variant	NM_005204.4(MAP3K8):c.770G>A (p.Ser257Asn)	not provided [RCV003570397]	uncertain significance	10	30451641	30451641	Human		name
404985690	CV3001408	single nucleotide variant	NM_005204.4(MAP3K8):c.667G>A (p.Gly223Arg)	not provided [RCV003691803]	uncertain significance	10	30450420	30450420	Human		name
405165434	CV3059537	single nucleotide variant	NM_005204.4(MAP3K8):c.964A>G (p.Thr322Ala)	not provided [RCV003727404]	uncertain significance	10	30458174	30458174	Human		name
405219294	CV3063318	single nucleotide variant	NM_005204.4(MAP3K8):c.831G>A (p.Met277Ile)	not provided [RCV003733067]\|not specified [RCV004374122]	uncertain significance	10	30451702	30451702	Human		name
405219681	CV3063396	single nucleotide variant	NM_005204.4(MAP3K8):c.442G>A (p.Ala148Thr)	not provided [RCV003733119]	uncertain significance	10	30447887	30447887	Human		name
405103748	CV3116344	single nucleotide variant	NM_005204.4(MAP3K8):c.826C>G (p.Gln276Glu)	not provided [RCV003812060]	uncertain significance	10	30451697	30451697	Human		name
402464465	CV3177048	single nucleotide variant	NM_005204.4(MAP3K8):c.597G>C (p.Trp199Cys)	not provided [RCV003872679]	uncertain significance	10	30450350	30450350	Human		name
405273484	CV3197796	single nucleotide variant	NM_005204.4(MAP3K8):c.784A>C (p.Met262Leu)	MAP3K8-related disorder [RCV003901760]	uncertain significance	10	30451655	30451655	Human		name , trait , alternate_id
597847503	CV3736721	single nucleotide variant	NM_005204.4(MAP3K8):c.358C>T (p.Arg120Cys)	not provided [RCV005065880]	uncertain significance	10	30447803	30447803	Human		name
597830561	CV3743098	single nucleotide variant	NM_005204.4(MAP3K8):c.343A>G (p.Thr115Ala)	not provided [RCV005062106]	uncertain significance	10	30447788	30447788	Human		name
597879251	CV3744493	single nucleotide variant	NM_005204.4(MAP3K8):c.841G>C (p.Val281Leu)	not provided [RCV005069707]	uncertain significance	10	30451712	30451712	Human		name
597861578	CV3770241	single nucleotide variant	NM_005204.4(MAP3K8):c.437G>A (p.Arg146Gln)	not provided [RCV005106094]	uncertain significance	10	30447882	30447882	Human		name
597958011	CV3814517	single nucleotide variant	NM_005204.4(MAP3K8):c.718G>A (p.Gly240Arg)	not provided [RCV005162848]	uncertain significance	10	30450471	30450471	Human		name
597975619	CV3828605	single nucleotide variant	NM_005204.4(MAP3K8):c.308C>T (p.Pro103Leu)	not provided [RCV005169234]	uncertain significance	10	30439246	30439246	Human		name
597913723	CV3833835	single nucleotide variant	NM_005204.4(MAP3K8):c.673A>G (p.Met225Val)	not provided [RCV005183194]	uncertain significance	10	30450426	30450426	Human		name
597912550	CV3834274	single nucleotide variant	NM_005204.4(MAP3K8):c.562G>C (p.Glu188Gln)	not provided [RCV005183036]	uncertain significance	10	30450315	30450315	Human		name
597903225	CV3851599	single nucleotide variant	NM_005204.4(MAP3K8):c.366A>T (p.Gln122His)	not provided [RCV005202376]	uncertain significance	10	30447811	30447811	Human		name
151742701	CV1353137	single nucleotide variant	NM_005204.4(MAP3K8):c.1339G>A (p.Asp447Asn)	MAP3K8-related disorder [RCV003923352]\|not provided [RCV001893427]	likely benign\|uncertain significance	10	30460771	30460771	Human	1	name , trait , alternate_id
151879878	CV1388333	single nucleotide variant	NM_005204.4(MAP3K8):c.1169C>T (p.Pro390Leu)	not provided [RCV001982376]	uncertain significance	10	30459397	30459397	Human		name
151869399	CV1415911	single nucleotide variant	NM_005204.4(MAP3K8):c.1065T>A (p.Asp355Glu)	not provided [RCV001884945]	uncertain significance	10	30459293	30459293	Human		name
151824758	CV1425047	single nucleotide variant	NM_005204.4(MAP3K8):c.1367A>G (p.Asn456Ser)	not provided [RCV001901225]	uncertain significance	10	30460799	30460799	Human		name
151837547	CV1445198	single nucleotide variant	NM_005204.4(MAP3K8):c.1120A>G (p.Asn374Asp)	not provided [RCV001994356]	uncertain significance	10	30459348	30459348	Human		name
151832428	CV1447252	single nucleotide variant	NM_005204.4(MAP3K8):c.1324C>T (p.Arg442Cys)	not provided [RCV001880437]	uncertain significance	10	30460756	30460756	Human		name
151835151	CV1463239	single nucleotide variant	NM_005204.4(MAP3K8):c.1177G>C (p.Glu393Gln)	not provided [RCV001880703]	uncertain significance	10	30459405	30459405	Human		name
151766422	CV1470001	single nucleotide variant	NM_005204.4(MAP3K8):c.1258C>T (p.Pro420Ser)	not provided [RCV001914551]	uncertain significance	10	30459486	30459486	Human		name
151891281	CV1496299	single nucleotide variant	NM_005204.4(MAP3K8):c.1388C>T (p.Thr463Met)	not provided [RCV001888665]	uncertain significance	10	30460820	30460820	Human		name
151861191	CV1511161	single nucleotide variant	NM_005204.4(MAP3K8):c.1162C>G (p.Leu388Val)	not provided [RCV001959245]	uncertain significance	10	30459390	30459390	Human		name
152053389	CV1523723	single nucleotide variant	NM_005204.4(MAP3K8):c.1280C>T (p.Ser427Leu)	not provided [RCV002127499]	benign	10	30460712	30460712	Human		name
156373366	CV1953513	single nucleotide variant	NM_005204.4(MAP3K8):c.1402T>C (p.Ter468Arg)	not provided [RCV002582602]	uncertain significance	10	30460834	30460834	Human		name
156333584	CV1954273	single nucleotide variant	NM_005204.4(MAP3K8):c.1196A>T (p.Gln399Leu)	not provided [RCV002580132]	uncertain significance	10	30459424	30459424	Human		name
156174181	CV1968501	single nucleotide variant	NM_005204.4(MAP3K8):c.1133G>A (p.Arg378Lys)	not provided [RCV002594863]	uncertain significance	10	30459361	30459361	Human		name
156403103	CV1993039	single nucleotide variant	NM_005204.4(MAP3K8):c.1348G>A (p.Ala450Thr)	not provided [RCV002657782]	uncertain significance	10	30460780	30460780	Human		name
156174686	CV2000263	single nucleotide variant	NM_005204.4(MAP3K8):c.1129C>T (p.Pro377Ser)	not provided [RCV002642832]	uncertain significance	10	30459357	30459357	Human		name
156089095	CV2008893	single nucleotide variant	NM_005204.4(MAP3K8):c.1379G>T (p.Gly460Val)	not provided [RCV002706247]	uncertain significance	10	30460811	30460811	Human		name
155915260	CV2033370	single nucleotide variant	NM_005204.4(MAP3K8):c.1223G>A (p.Arg408His)	not provided [RCV002750429]	uncertain significance	10	30459451	30459451	Human		name
156002417	CV2045646	single nucleotide variant	NM_005204.4(MAP3K8):c.1297G>A (p.Glu433Lys)	not provided [RCV002756272]	uncertain significance	10	30460729	30460729	Human		name
155914176	CV2242636	single nucleotide variant	NM_005204.4(MAP3K8):c.1174A>G (p.Arg392Gly)	not specified [RCV004113692]	uncertain significance	10	30459402	30459402	Human		name
156199739	CV2313014	single nucleotide variant	NM_005204.4(MAP3K8):c.1138G>A (p.Ala380Thr)	not specified [RCV004159512]	uncertain significance	10	30459366	30459366	Human		name
156361109	CV2326376	single nucleotide variant	NM_005204.4(MAP3K8):c.1046C>G (p.Pro349Arg)	not specified [RCV004182953]	uncertain significance	10	30459274	30459274	Human		name
329360967	CV2463153	single nucleotide variant	NM_005204.4(MAP3K8):c.1079G>T (p.Gly360Val)	not specified [RCV004274943]	uncertain significance	10	30459307	30459307	Human		name
405072994	CV2872970	single nucleotide variant	NM_005204.4(MAP3K8):c.1121A>G (p.Asn374Ser)	not provided [RCV003548643]	uncertain significance	10	30459349	30459349	Human		name
405216271	CV2876325	single nucleotide variant	NM_005204.4(MAP3K8):c.1090C>G (p.Leu364Val)	not provided [RCV003553237]	uncertain significance	10	30459318	30459318	Human		name
402507638	CV2880691	single nucleotide variant	NM_005204.4(MAP3K8):c.1285A>C (p.Thr429Pro)	not provided [RCV003546392]	uncertain significance	10	30460717	30460717	Human		name
405026202	CV2889847	single nucleotide variant	NM_005204.4(MAP3K8):c.1358G>C (p.Gly453Ala)	not provided [RCV003577999]	uncertain significance	10	30460790	30460790	Human		name
405149530	CV2891997	single nucleotide variant	NM_005204.4(MAP3K8):c.1250T>A (p.Leu417Gln)	not provided [RCV003561626]	uncertain significance	10	30459478	30459478	Human		name
405129763	CV2962283	single nucleotide variant	NM_005204.4(MAP3K8):c.1222C>A (p.Arg408Ser)	not provided [RCV003668273]\|not specified [RCV005377454]	uncertain significance	10	30459450	30459450	Human		name
405244033	CV3053879	single nucleotide variant	NM_005204.4(MAP3K8):c.1072A>C (p.Ser358Arg)	not provided [RCV003719793]	uncertain significance	10	30459300	30459300	Human		name
405162233	CV3062683	single nucleotide variant	NM_005204.4(MAP3K8):c.1189C>T (p.Arg397Cys)	not provided [RCV003727180]	uncertain significance	10	30459417	30459417	Human		name
405232178	CV3144641	single nucleotide variant	NM_005204.4(MAP3K8):c.1175G>A (p.Arg392Lys)	not provided [RCV003853094]\|not specified [RCV005377593]	uncertain significance	10	30459403	30459403	Human		name
405248168	CV3159254	single nucleotide variant	NM_005204.4(MAP3K8):c.1225A>G (p.Lys409Glu)	not provided [RCV003869399]	uncertain significance	10	30459453	30459453	Human		name
405249341	CV3170053	single nucleotide variant	NM_005204.4(MAP3K8):c.1108G>A (p.Glu370Lys)	not provided [RCV003869682]	uncertain significance	10	30459336	30459336	Human		name
405811275	CV3284865	single nucleotide variant	NM_005204.4(MAP3K8):c.1022A>G (p.Tyr341Cys)	not specified [RCV004408401]	uncertain significance	10	30458232	30458232	Human		name
597627324	CV3700196	single nucleotide variant	NM_005204.4(MAP3K8):c.1376G>A (p.Arg459Gln)	not specified [RCV004938908]	uncertain significance	10	30460808	30460808	Human		name
597947025	CV3790564	single nucleotide variant	NM_005204.4(MAP3K8):c.1242G>T (p.Arg414Ser)	not provided [RCV005134972]	uncertain significance	10	30459470	30459470	Human		name
597861319	CV3813510	single nucleotide variant	NM_005204.4(MAP3K8):c.1222C>T (p.Arg408Cys)	not provided [RCV005146772]	uncertain significance	10	30459450	30459450	Human		name
597974542	CV3831705	single nucleotide variant	NM_005204.4(MAP3K8):c.1169C>G (p.Pro390Arg)	not provided [RCV005168644]	uncertain significance	10	30459397	30459397	Human		name
597963357	CV3841503	single nucleotide variant	NM_005204.4(MAP3K8):c.1127G>A (p.Arg376His)	not provided [RCV005193607]	uncertain significance	10	30459355	30459355	Human		name
597948727	CV3848735	single nucleotide variant	NM_005204.4(MAP3K8):c.1382C>A (p.Pro461Gln)	not provided [RCV005189672]	uncertain significance	10	30460814	30460814	Human		name

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