Map1a Variant Search Result - Rat Genome Database

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273 records found for search term Map1a

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156088715	CV2359276	single nucleotide variant	NM_002373.6(MAP1A):c.10G>A (p.Val4Met)	not specified [RCV004212564]	uncertain significance	15	43521483	43521483	Human		name
329360918	CV2439885	single nucleotide variant	NM_002373.6(MAP1A):c.167A>G (p.Asn56Ser)	not specified [RCV004257923]	uncertain significance	15	43521640	43521640	Human		name
15199236	CV726081	single nucleotide variant	NM_002373.6(MAP1A):c.1446A>G (p.Gly482=)	not provided [RCV000890579]	benign\|likely benign	15	43522919	43522919	Human		name
15152193	CV754459	single nucleotide variant	NM_002373.6(MAP1A):c.2349A>T (p.Pro783=)	not provided [RCV000923824]	likely benign	15	43523822	43523822	Human		name
8635469	CV90690	single nucleotide variant	NM_002373.5(MAP1A):c.2250C>T (p.Ile750=)	Malignant melanoma [RCV000070788]	not provided	15	43523723	43523723	Human		name
156259731	CV2216260	single nucleotide variant	NM_002373.6(MAP1A):c.498A>C (p.Leu166Phe)	not specified [RCV004097206]	uncertain significance	15	43521971	43521971	Human		name
156259746	CV2216261	single nucleotide variant	NM_002373.6(MAP1A):c.499A>C (p.Asn167His)	not specified [RCV004097207]	uncertain significance	15	43521972	43521972	Human		name
156303031	CV2258767	single nucleotide variant	NM_002373.6(MAP1A):c.411C>G (p.Phe137Leu)	not specified [RCV004117999]	uncertain significance	15	43521884	43521884	Human		name
156064345	CV2272423	single nucleotide variant	NM_002373.6(MAP1A):c.494A>C (p.His165Pro)	not specified [RCV004133344]	uncertain significance	15	43521967	43521967	Human		name
155911275	CV2303787	single nucleotide variant	NM_002373.6(MAP1A):c.449G>A (p.Arg150Gln)	not specified [RCV004163628]	uncertain significance	15	43521922	43521922	Human		name
401860038	CV2765445	single nucleotide variant	NM_002373.6(MAP1A):c.770A>G (p.Asn257Ser)	not specified [RCV004341763]	uncertain significance	15	43522243	43522243	Human		name
401916238	CV2817516	single nucleotide variant	NM_002373.6(MAP1A):c.6816G>A (p.Ala2272=)	not provided [RCV003400933]	likely benign	15	43528289	43528289	Human		name
405258817	CV3215103	single nucleotide variant	NM_002373.6(MAP1A):c.7110A>G (p.Pro2370=)	MAP1A-related disorder [RCV003942160]	likely benign	15	43528583	43528583	Human		name , trait , alternate_id
405657181	CV3288463	single nucleotide variant	NM_002373.6(MAP1A):c.386C>T (p.Ser129Phe)	not specified [RCV004416059]	uncertain significance	15	43521859	43521859	Human		name
405657254	CV3288486	single nucleotide variant	NM_002373.6(MAP1A):c.851G>A (p.Arg284Gln)	not specified [RCV004416082]	uncertain significance	15	43522324	43522324	Human		name
405657257	CV3288487	single nucleotide variant	NM_002373.6(MAP1A):c.869G>A (p.Arg290His)	not specified [RCV004416083]	uncertain significance	15	43522342	43522342	Human		name
407493522	CV3446370	single nucleotide variant	NM_002373.6(MAP1A):c.891G>C (p.Lys297Asn)	not specified [RCV004642755]	uncertain significance	15	43522364	43522364	Human		name
407493567	CV3446384	single nucleotide variant	NM_002373.6(MAP1A):c.517G>A (p.Ala173Thr)	not specified [RCV004642766]	uncertain significance	15	43521990	43521990	Human		name
597626734	CV3702857	single nucleotide variant	NM_002373.6(MAP1A):c.698A>G (p.Asn233Ser)	not specified [RCV004938635]	uncertain significance	15	43522171	43522171	Human		name
597626411	CV3702872	single nucleotide variant	NM_002373.6(MAP1A):c.298G>A (p.Gly100Arg)	not specified [RCV004938649]	uncertain significance	15	43521771	43521771	Human		name
597626440	CV3702882	single nucleotide variant	NM_002373.6(MAP1A):c.370G>A (p.Val124Met)	not specified [RCV004938658]	uncertain significance	15	43521843	43521843	Human		name
597626454	CV3702886	single nucleotide variant	NM_002373.6(MAP1A):c.958A>G (p.Lys320Glu)	not specified [RCV004938662]	uncertain significance	15	43522431	43522431	Human		name
597626475	CV3702893	single nucleotide variant	NM_002373.6(MAP1A):c.590G>A (p.Arg197Gln)	not specified [RCV004938668]	uncertain significance	15	43522063	43522063	Human		name
598196472	CV3988534	single nucleotide variant	NM_002373.6(MAP1A):c.892G>A (p.Asp298Asn)	not specified [RCV005375273]	uncertain significance	15	43522365	43522365	Human		name
598196484	CV3988537	single nucleotide variant	NM_002373.6(MAP1A):c.461G>C (p.Arg154Pro)	not specified [RCV005375275]	uncertain significance	15	43521934	43521934	Human		name
15131031	CV714460	single nucleotide variant	NM_002373.6(MAP1A):c.3933C>T (p.Ser1311=)	not provided [RCV000964535]	benign\|likely benign	15	43525406	43525406	Human		name
15184169	CV739632	single nucleotide variant	NM_002373.6(MAP1A):c.4632A>G (p.Ser1544=)	not provided [RCV000908219]	benign	15	43526105	43526105	Human		name
15136556	CV739633	single nucleotide variant	NM_002373.6(MAP1A):c.7908T>C (p.Pro2636=)	not provided [RCV000898648]	likely benign	15	43529381	43529381	Human		name
15152197	CV754460	single nucleotide variant	NM_002373.6(MAP1A):c.3456C>A (p.Ser1152=)	not provided [RCV000923825]	likely benign	15	43524929	43524929	Human		name
15152202	CV754461	single nucleotide variant	NM_002373.6(MAP1A):c.6456A>G (p.Ser2152=)	not provided [RCV000923826]	likely benign	15	43527929	43527929	Human		name
8635468	CV90689	single nucleotide variant	NM_002373.5(MAP1A):c.806G>A (p.Gly269Glu)	Malignant melanoma [RCV000070787]	not provided	15	43522279	43522279	Human		name
8635470	CV90691	single nucleotide variant	NM_002373.5(MAP1A):c.4245A>G (p.Leu1415=)	Malignant melanoma [RCV000070789]	not provided	15	43525718	43525718	Human		name
155959058	CV2193727	single nucleotide variant	NM_002373.6(MAP1A):c.1993C>A (p.His665Asn)	not specified [RCV004074491]	uncertain significance	15	43523466	43523466	Human		name
156373861	CV2201489	single nucleotide variant	NM_002373.6(MAP1A):c.1765G>T (p.Val589Leu)	not specified [RCV004079637]	uncertain significance	15	43523238	43523238	Human		name
156139468	CV2212079	single nucleotide variant	NM_002373.6(MAP1A):c.2749G>A (p.Val917Met)	not specified [RCV004088988]	uncertain significance	15	43524222	43524222	Human		name
155926023	CV2230545	single nucleotide variant	NM_002373.6(MAP1A):c.2083A>G (p.Ser695Gly)	not specified [RCV004097515]	likely benign	15	43523556	43523556	Human		name
156053866	CV2243015	single nucleotide variant	NM_002373.6(MAP1A):c.2035G>C (p.Gly679Arg)	not specified [RCV004109936]	uncertain significance	15	43523508	43523508	Human		name
156001050	CV2257812	single nucleotide variant	NM_002373.6(MAP1A):c.1654A>G (p.Thr552Ala)	not specified [RCV004599499]	uncertain significance	15	43523127	43523127	Human		name
156112987	CV2263720	single nucleotide variant	NM_002373.6(MAP1A):c.2701C>G (p.Leu901Val)	not specified [RCV004136011]	uncertain significance	15	43524174	43524174	Human		name
156052938	CV2269458	single nucleotide variant	NM_002373.6(MAP1A):c.1504C>G (p.Pro502Ala)	not specified [RCV004124573]	uncertain significance	15	43522977	43522977	Human		name
156256398	CV2277577	single nucleotide variant	NM_002373.6(MAP1A):c.2050C>T (p.His684Tyr)	not specified [RCV004145262]	uncertain significance	15	43523523	43523523	Human		name
156074515	CV2281447	single nucleotide variant	NM_002373.6(MAP1A):c.2564C>A (p.Thr855Lys)	not specified [RCV004153775]	uncertain significance	15	43524037	43524037	Human		name
155986538	CV2282612	single nucleotide variant	NM_002373.6(MAP1A):c.2147C>T (p.Ser716Leu)	not specified [RCV004135172]	uncertain significance	15	43523620	43523620	Human		name
156082827	CV2292968	single nucleotide variant	NM_002373.6(MAP1A):c.1722G>T (p.Gln574His)	not specified [RCV004148453]	uncertain significance	15	43523195	43523195	Human		name
156016180	CV2295206	single nucleotide variant	NM_002373.6(MAP1A):c.1918G>A (p.Ala640Thr)	not specified [RCV004158594]	uncertain significance	15	43523391	43523391	Human		name
156015432	CV2298821	single nucleotide variant	NM_002373.6(MAP1A):c.1815C>G (p.Ser605Arg)	not specified [RCV004156373]	uncertain significance	15	43523288	43523288	Human		name
156168898	CV2320127	single nucleotide variant	NM_002373.6(MAP1A):c.2396G>C (p.Gly799Ala)	not specified [RCV004167971]	uncertain significance	15	43523869	43523869	Human		name
156361483	CV2326598	single nucleotide variant	NM_002373.6(MAP1A):c.2980A>G (p.Met994Val)	not specified [RCV004183140]	uncertain significance	15	43524453	43524453	Human		name
156094738	CV2398874	single nucleotide variant	NM_002373.6(MAP1A):c.1010G>A (p.Arg337Gln)	not specified [RCV004245195]	uncertain significance	15	43522483	43522483	Human		name
156005281	CV2401074	single nucleotide variant	NM_002373.6(MAP1A):c.2992C>T (p.Pro998Ser)	not specified [RCV004245646]	uncertain significance	15	43524465	43524465	Human		name
329360456	CV2442811	single nucleotide variant	NM_002373.6(MAP1A):c.2020G>A (p.Ala674Thr)	not specified [RCV004251636]	uncertain significance	15	43523493	43523493	Human		name
329371325	CV2458079	single nucleotide variant	NM_002373.6(MAP1A):c.2329G>A (p.Gly777Arg)	not specified [RCV004271906]	uncertain significance	15	43523802	43523802	Human		name
329374719	CV2470684	single nucleotide variant	NM_002373.6(MAP1A):c.1442C>T (p.Pro481Leu)	not specified [RCV004275934]	uncertain significance	15	43522915	43522915	Human		name
401737299	CV2679278	single nucleotide variant	NM_002373.6(MAP1A):c.2021C>T (p.Ala674Val)	not specified [RCV004285824]	uncertain significance	15	43523494	43523494	Human		name
401744128	CV2696941	single nucleotide variant	NM_002373.6(MAP1A):c.1872G>C (p.Glu624Asp)	not specified [RCV004292938]	uncertain significance	15	43523345	43523345	Human		name
401767294	CV2718452	single nucleotide variant	NM_002373.6(MAP1A):c.1636C>G (p.Leu546Val)	not specified [RCV004318266]	uncertain significance	15	43523109	43523109	Human		name
401886028	CV2771575	single nucleotide variant	NM_002373.6(MAP1A):c.1477C>T (p.Arg493Cys)	not specified [RCV004348597]	uncertain significance	15	43522950	43522950	Human		name
401876143	CV2777676	single nucleotide variant	NM_002373.6(MAP1A):c.2315C>T (p.Thr772Ile)	not specified [RCV004343512]	uncertain significance	15	43523788	43523788	Human		name
401885090	CV2786671	single nucleotide variant	NM_002373.6(MAP1A):c.1347G>T (p.Arg449Ser)	not specified [RCV004363798]	uncertain significance	15	43522820	43522820	Human		name
401864784	CV2791359	single nucleotide variant	NM_002373.6(MAP1A):c.2820G>T (p.Glu940Asp)	not specified [RCV004358767]	uncertain significance	15	43524293	43524293	Human		name
404980117	CV2850431	single nucleotide variant	NM_002373.6(MAP1A):c.1700G>C (p.Gly567Ala)	not provided [RCV003488014]	uncertain significance	15	43523173	43523173	Human		name
405279615	CV3206995	single nucleotide variant	NM_002373.6(MAP1A):c.2318A>G (p.Tyr773Cys)	MAP1A-related disorder [RCV003919549]	likely benign	15	43523791	43523791	Human		name , trait , alternate_id
405657043	CV3288443	single nucleotide variant	NM_002373.6(MAP1A):c.1013A>G (p.Glu338Gly)	not specified [RCV004416039]	uncertain significance	15	43522486	43522486	Human		name
405657045	CV3288444	single nucleotide variant	NM_002373.6(MAP1A):c.1033G>C (p.Ala345Pro)	not specified [RCV004416040]	uncertain significance	15	43522506	43522506	Human		name
405657050	CV3288446	single nucleotide variant	NM_002373.6(MAP1A):c.1577C>T (p.Ser526Phe)	not specified [RCV004416042]	uncertain significance	15	43523050	43523050	Human		name
405657054	CV3288447	single nucleotide variant	NM_002373.6(MAP1A):c.1619G>T (p.Arg540Leu)	not specified [RCV004416043]	uncertain significance	15	43523092	43523092	Human		name
405657130	CV3288448	single nucleotide variant	NM_002373.6(MAP1A):c.1712C>T (p.Thr571Ile)	not specified [RCV004416044]	uncertain significance	15	43523185	43523185	Human		name
405657133	CV3288449	single nucleotide variant	NM_002373.6(MAP1A):c.1760A>G (p.Glu587Gly)	not specified [RCV004416045]	uncertain significance	15	43523233	43523233	Human		name
405657135	CV3288450	single nucleotide variant	NM_002373.6(MAP1A):c.1772A>G (p.Lys591Arg)	not specified [RCV004416046]	uncertain significance	15	43523245	43523245	Human		name
405657138	CV3288451	single nucleotide variant	NM_002373.6(MAP1A):c.1799C>G (p.Pro600Arg)	not specified [RCV004416047]	uncertain significance	15	43523272	43523272	Human		name
405657141	CV3288452	single nucleotide variant	NM_002373.6(MAP1A):c.2276C>T (p.Pro759Leu)	not specified [RCV004416048]	uncertain significance	15	43523749	43523749	Human		name
405657144	CV3288453	single nucleotide variant	NM_002373.6(MAP1A):c.2303T>G (p.Phe768Cys)	not specified [RCV004416049]	uncertain significance	15	43523776	43523776	Human		name
405657147	CV3288454	single nucleotide variant	NM_002373.6(MAP1A):c.2510A>G (p.Lys837Arg)	not specified [RCV004416050]	uncertain significance	15	43523983	43523983	Human		name
405657150	CV3288455	single nucleotide variant	NM_002373.6(MAP1A):c.2731C>T (p.Pro911Ser)	not specified [RCV004416051]	uncertain significance	15	43524204	43524204	Human		name
405657154	CV3288456	single nucleotide variant	NM_002373.6(MAP1A):c.2805G>C (p.Glu935Asp)	not specified [RCV004416052]	uncertain significance	15	43524278	43524278	Human		name
405657157	CV3288457	single nucleotide variant	NM_002373.6(MAP1A):c.2825A>T (p.Glu942Val)	not specified [RCV004416053]	uncertain significance	15	43524298	43524298	Human		name
407493508	CV3446366	single nucleotide variant	NM_002373.6(MAP1A):c.2300G>C (p.Arg767Thr)	not specified [RCV004642752]	uncertain significance	15	43523773	43523773	Human		name
407493516	CV3446368	single nucleotide variant	NM_002373.6(MAP1A):c.2285G>A (p.Arg762His)	not specified [RCV004642754]	uncertain significance	15	43523758	43523758	Human		name
597626773	CV3702844	single nucleotide variant	NM_002373.6(MAP1A):c.2780T>C (p.Ile927Thr)	not specified [RCV004938623]	uncertain significance	15	43524253	43524253	Human		name
597626770	CV3702846	single nucleotide variant	NM_002373.6(MAP1A):c.1120C>T (p.Pro374Ser)	not specified [RCV004938624]	uncertain significance	15	43522593	43522593	Human		name
597626765	CV3702848	single nucleotide variant	NM_002373.6(MAP1A):c.2549C>A (p.Ser850Tyr)	not specified [RCV004938626]	uncertain significance	15	43524022	43524022	Human		name
597626731	CV3702858	single nucleotide variant	NM_002373.6(MAP1A):c.2284C>T (p.Arg762Cys)	not specified [RCV004938636]	uncertain significance	15	43523757	43523757	Human		name
597626728	CV3702859	single nucleotide variant	NM_002373.6(MAP1A):c.2288C>T (p.Pro763Leu)	not specified [RCV004938637]	uncertain significance	15	43523761	43523761	Human		name
597626522	CV3702864	single nucleotide variant	NM_002373.6(MAP1A):c.1079A>G (p.Glu360Gly)	not specified [RCV004938641]	uncertain significance	15	43522552	43522552	Human		name
597626396	CV3702868	single nucleotide variant	NM_002373.6(MAP1A):c.2134G>A (p.Glu712Lys)	not specified [RCV004938645]	uncertain significance	15	43523607	43523607	Human		name
597626458	CV3702887	single nucleotide variant	NM_002373.6(MAP1A):c.1042G>A (p.Ala348Thr)	not specified [RCV004938663]	uncertain significance	15	43522515	43522515	Human		name
598165886	CV3988528	single nucleotide variant	NM_002373.6(MAP1A):c.1349A>G (p.Lys450Arg)	not specified [RCV005369245]	uncertain significance	15	43522822	43522822	Human		name
598196490	CV3988538	single nucleotide variant	NM_002373.6(MAP1A):c.1929A>C (p.Glu643Asp)	not specified [RCV005375276]	uncertain significance	15	43523402	43523402	Human		name
598165922	CV3988545	single nucleotide variant	NM_002373.6(MAP1A):c.2294C>T (p.Pro765Leu)	not specified [RCV005369250]	uncertain significance	15	43523767	43523767	Human		name
598196542	CV3988551	single nucleotide variant	NM_002373.6(MAP1A):c.1019T>A (p.Val340Glu)	not specified [RCV005375284]	uncertain significance	15	43522492	43522492	Human		name
598165937	CV3988552	single nucleotide variant	NM_002373.6(MAP1A):c.1635G>T (p.Leu545Phe)	not specified [RCV005369253]	uncertain significance	15	43523108	43523108	Human		name
598196562	CV3988555	single nucleotide variant	NM_002373.6(MAP1A):c.2301A>T (p.Arg767Ser)	not specified [RCV005375287]	uncertain significance	15	43523774	43523774	Human		name
13530603	CV512139	single nucleotide variant	NM_002373.6(MAP1A):c.2293C>T (p.Pro765Ser)	Inborn genetic diseases [RCV000622626]	uncertain significance	15	43523766	43523766	Human	1	name
156398434	CV2200790	single nucleotide variant	NM_002373.6(MAP1A):c.6845C>T (p.Ala2282Val)	not specified [RCV004081429]	uncertain significance	15	43528318	43528318	Human		name
155916969	CV2202123	single nucleotide variant	NM_002373.6(MAP1A):c.7526C>T (p.Ser2509Leu)	not specified [RCV004078077]	uncertain significance	15	43528999	43528999	Human		name
155964668	CV2210029	single nucleotide variant	NM_002373.6(MAP1A):c.5740G>A (p.Gly1914Arg)	not specified [RCV004076460]	uncertain significance	15	43527213	43527213	Human		name
156330096	CV2213988	single nucleotide variant	NM_002373.6(MAP1A):c.7439G>A (p.Arg2480His)	not specified [RCV004083706]	uncertain significance	15	43528912	43528912	Human		name
156091963	CV2216699	single nucleotide variant	NM_002373.6(MAP1A):c.4323G>T (p.Lys1441Asn)	not specified [RCV004083150]	uncertain significance	15	43525796	43525796	Human		name
156238649	CV2217074	single nucleotide variant	NM_002373.6(MAP1A):c.4301A>C (p.Lys1434Thr)	not specified [RCV004085752]	uncertain significance	15	43525774	43525774	Human		name
156281568	CV2220570	single nucleotide variant	NM_002373.6(MAP1A):c.3743A>G (p.His1248Arg)	not specified [RCV004097769]	uncertain significance	15	43525216	43525216	Human		name
156126974	CV2223734	single nucleotide variant	NM_002373.6(MAP1A):c.6623C>T (p.Pro2208Leu)	not specified [RCV004093820]	uncertain significance	15	43528096	43528096	Human		name
156278266	CV2227504	single nucleotide variant	NM_002373.6(MAP1A):c.5581C>T (p.Pro1861Ser)	not specified [RCV004092158]	uncertain significance	15	43527054	43527054	Human		name
155940896	CV2232298	single nucleotide variant	NM_002373.6(MAP1A):c.2999C>T (p.Ser1000Phe)	not specified [RCV004105075]	uncertain significance	15	43524472	43524472	Human		name
155901555	CV2242053	single nucleotide variant	NM_002373.6(MAP1A):c.5198G>C (p.Gly1733Ala)	not specified [RCV004108987]	uncertain significance	15	43526671	43526671	Human		name
155969680	CV2244629	single nucleotide variant	NM_002373.6(MAP1A):c.4145C>T (p.Pro1382Leu)	not specified [RCV004102345]	uncertain significance	15	43525618	43525618	Human		name
155987352	CV2248079	single nucleotide variant	NM_002373.6(MAP1A):c.4145C>G (p.Pro1382Arg)	not specified [RCV004115355]	uncertain significance	15	43525618	43525618	Human		name
156075118	CV2248223	single nucleotide variant	NM_002373.6(MAP1A):c.8168G>A (p.Ser2723Asn)	not specified [RCV004117611]	uncertain significance	15	43529782	43529782	Human		name
156208716	CV2250142	single nucleotide variant	NM_002373.6(MAP1A):c.5839G>A (p.Glu1947Lys)	not specified [RCV004116950]	uncertain significance	15	43527312	43527312	Human		name
156099202	CV2250654	single nucleotide variant	NM_002373.6(MAP1A):c.7394A>C (p.Asp2465Ala)	not specified [RCV004129281]	uncertain significance	15	43528867	43528867	Human		name
156136798	CV2253336	single nucleotide variant	NM_002373.6(MAP1A):c.5797A>G (p.Lys1933Glu)	not specified [RCV004123167]	uncertain significance	15	43527270	43527270	Human		name
156310158	CV2260005	single nucleotide variant	NM_002373.6(MAP1A):c.5704T>C (p.Tyr1902His)	not specified [RCV004119019]	uncertain significance	15	43527177	43527177	Human		name
156052950	CV2269459	single nucleotide variant	NM_002373.6(MAP1A):c.6935C>T (p.Ala2312Val)	not specified [RCV004124574]	uncertain significance	15	43528408	43528408	Human		name
156259560	CV2274127	single nucleotide variant	NM_002373.6(MAP1A):c.4549G>A (p.Glu1517Lys)	not specified [RCV004134766]	uncertain significance	15	43526022	43526022	Human		name
155984209	CV2274510	single nucleotide variant	NM_002373.6(MAP1A):c.7333C>T (p.Arg2445Cys)	not specified [RCV004138922]	likely benign	15	43528806	43528806	Human		name
156258389	CV2277741	single nucleotide variant	NM_002373.6(MAP1A):c.3593C>A (p.Ser1198Tyr)	not specified [RCV004147180]	uncertain significance	15	43525066	43525066	Human		name
156067609	CV2284829	single nucleotide variant	NM_002373.6(MAP1A):c.7547C>G (p.Pro2516Arg)	not specified [RCV004143003]	uncertain significance	15	43529020	43529020	Human		name
156085679	CV2289852	single nucleotide variant	NM_002373.6(MAP1A):c.5560C>A (p.Pro1854Thr)	not specified [RCV004150516]	uncertain significance	15	43527033	43527033	Human		name
156273839	CV2293679	single nucleotide variant	NM_002373.6(MAP1A):c.5630C>G (p.Ser1877Cys)	not specified [RCV004153180]	uncertain significance	15	43527103	43527103	Human		name
156091073	CV2302626	single nucleotide variant	NM_002373.6(MAP1A):c.3871A>T (p.Ser1291Cys)	not specified [RCV004160786]	uncertain significance	15	43525344	43525344	Human		name
156097788	CV2310296	single nucleotide variant	NM_002373.6(MAP1A):c.3287A>G (p.Lys1096Arg)	not specified [RCV004157039]	uncertain significance	15	43524760	43524760	Human		name
156264693	CV2312121	single nucleotide variant	NM_002373.6(MAP1A):c.3553C>T (p.Arg1185Cys)	not specified [RCV004165034]	uncertain significance	15	43525026	43525026	Human		name
156211583	CV2314595	single nucleotide variant	NM_002373.6(MAP1A):c.7042A>T (p.Ser2348Cys)	not specified [RCV004168678]	uncertain significance	15	43528515	43528515	Human		name
156150738	CV2318699	single nucleotide variant	NM_002373.6(MAP1A):c.3559C>T (p.Pro1187Ser)	not specified [RCV004173592]	uncertain significance	15	43525032	43525032	Human		name
156362186	CV2323075	single nucleotide variant	NM_002373.6(MAP1A):c.6127G>A (p.Val2043Ile)	not specified [RCV004187493]	uncertain significance	15	43527600	43527600	Human		name
156351519	CV2323775	single nucleotide variant	NM_002373.6(MAP1A):c.6473G>A (p.Arg2158Gln)	not specified [RCV004176323]	uncertain significance	15	43527946	43527946	Human		name
156359588	CV2328242	single nucleotide variant	NM_002373.6(MAP1A):c.7720C>T (p.Arg2574Cys)	not specified [RCV004173329]	uncertain significance	15	43529193	43529193	Human		name
156052744	CV2329042	single nucleotide variant	NM_002373.6(MAP1A):c.7316C>G (p.Thr2439Ser)	not specified [RCV004180322]	uncertain significance	15	43528789	43528789	Human		name
156285373	CV2334836	single nucleotide variant	NM_002373.6(MAP1A):c.6622C>T (p.Pro2208Ser)	not specified [RCV004181946]	uncertain significance	15	43528095	43528095	Human		name
156201519	CV2338480	single nucleotide variant	NM_002373.6(MAP1A):c.7436G>A (p.Arg2479Gln)	not specified [RCV004188520]	uncertain significance	15	43528909	43528909	Human		name
156085662	CV2340451	single nucleotide variant	NM_002373.6(MAP1A):c.6026G>A (p.Arg2009Gln)	not specified [RCV004197178]	uncertain significance	15	43527499	43527499	Human		name
156240845	CV2350373	single nucleotide variant	NM_002373.6(MAP1A):c.7268C>T (p.Pro2423Leu)	not specified [RCV004202317]	uncertain significance	15	43528741	43528741	Human		name
155918749	CV2362703	single nucleotide variant	NM_002373.6(MAP1A):c.7017C>G (p.Cys2339Trp)	not specified [RCV004215345]	uncertain significance	15	43528490	43528490	Human		name
156017361	CV2370094	single nucleotide variant	NM_002373.6(MAP1A):c.4936G>A (p.Val1646Met)	not specified [RCV004210986]	uncertain significance	15	43526409	43526409	Human		name
155931262	CV2370867	single nucleotide variant	NM_002373.6(MAP1A):c.4609C>G (p.Gln1537Glu)	not specified [RCV004218610]	uncertain significance	15	43526082	43526082	Human		name
156079117	CV2375245	single nucleotide variant	NM_002373.6(MAP1A):c.6815C>T (p.Ala2272Val)	not specified [RCV004230277]	uncertain significance	15	43528288	43528288	Human		name
155936940	CV2376192	single nucleotide variant	NM_002373.6(MAP1A):c.4132G>A (p.Glu1378Lys)	not specified [RCV004220417]	uncertain significance	15	43525605	43525605	Human		name
155938706	CV2380914	single nucleotide variant	NM_002373.6(MAP1A):c.5729G>T (p.Arg1910Leu)	not specified [RCV004218456]	uncertain significance	15	43527202	43527202	Human		name
156031311	CV2380964	single nucleotide variant	NM_002373.6(MAP1A):c.6365C>G (p.Ala2122Gly)	not specified [RCV004220542]	uncertain significance	15	43527838	43527838	Human		name
156058788	CV2383462	single nucleotide variant	NM_002373.6(MAP1A):c.3328G>C (p.Gly1110Arg)	not specified [RCV004222477]	uncertain significance	15	43524801	43524801	Human		name
156040644	CV2384373	single nucleotide variant	NM_002373.6(MAP1A):c.3086C>T (p.Ser1029Phe)	not specified [RCV004229796]	uncertain significance	15	43524559	43524559	Human		name
156092300	CV2384920	single nucleotide variant	NM_002373.6(MAP1A):c.7874G>A (p.Arg2625Gln)	not specified [RCV004225790]	uncertain significance	15	43529347	43529347	Human		name
156000895	CV2391822	single nucleotide variant	NM_002373.6(MAP1A):c.7964C>A (p.Thr2655Asn)	not specified [RCV004235701]	uncertain significance	15	43529437	43529437	Human		name
156271281	CV2396143	single nucleotide variant	NM_002373.6(MAP1A):c.7126A>C (p.Lys2376Gln)	not specified [RCV004240112]	uncertain significance	15	43528599	43528599	Human		name
329376771	CV2428539	single nucleotide variant	NM_002373.6(MAP1A):c.5149G>C (p.Ala1717Pro)	not specified [RCV004253323]	uncertain significance	15	43526622	43526622	Human		name
329399210	CV2436388	single nucleotide variant	NM_002373.6(MAP1A):c.4222T>G (p.Leu1408Val)	not specified [RCV004251780]	uncertain significance	15	43525695	43525695	Human		name
329366159	CV2438173	single nucleotide variant	NM_002373.6(MAP1A):c.7883G>A (p.Arg2628His)	not specified [RCV004256948]	uncertain significance	15	43529356	43529356	Human		name
329363114	CV2445860	single nucleotide variant	NM_002373.6(MAP1A):c.6185T>G (p.Val2062Gly)	not specified [RCV004270476]	uncertain significance	15	43527658	43527658	Human		name
329401046	CV2446074	single nucleotide variant	NM_002373.6(MAP1A):c.5242C>T (p.Arg1748Trp)	not specified [RCV004270636]	uncertain significance	15	43526715	43526715	Human		name
401753815	CV2685068	single nucleotide variant	NM_002373.6(MAP1A):c.3368G>A (p.Arg1123Lys)	not specified [RCV004289647]	uncertain significance	15	43524841	43524841	Human		name
401758454	CV2694111	single nucleotide variant	NM_002373.6(MAP1A):c.5369G>A (p.Arg1790His)	not specified [RCV004302543]	uncertain significance	15	43526842	43526842	Human		name
401758611	CV2694189	single nucleotide variant	NM_002373.6(MAP1A):c.3204G>T (p.Arg1068Ser)	not specified [RCV004302611]	uncertain significance	15	43524677	43524677	Human		name
401758589	CV2700614	single nucleotide variant	NM_002373.6(MAP1A):c.7253G>C (p.Gly2418Ala)	not specified [RCV004313345]	likely benign	15	43528726	43528726	Human		name
401718042	CV2714494	single nucleotide variant	NM_002373.6(MAP1A):c.4257C>G (p.Asp1419Glu)	not specified [RCV004318016]	uncertain significance	15	43525730	43525730	Human		name
401771810	CV2722954	single nucleotide variant	NM_002373.6(MAP1A):c.5111G>A (p.Arg1704Gln)	not specified [RCV004327133]	uncertain significance	15	43526584	43526584	Human		name
401758067	CV2731666	single nucleotide variant	NM_002373.6(MAP1A):c.5383A>C (p.Ile1795Leu)	not specified [RCV004331770]	uncertain significance	15	43526856	43526856	Human		name
401872079	CV2754259	single nucleotide variant	NM_002373.6(MAP1A):c.7952C>A (p.Thr2651Lys)	not specified [RCV004334443]	uncertain significance	15	43529425	43529425	Human		name
401883503	CV2757946	single nucleotide variant	NM_002373.6(MAP1A):c.7258G>A (p.Gly2420Arg)	not specified [RCV004337080]	uncertain significance	15	43528731	43528731	Human		name
401899801	CV2762363	single nucleotide variant	NM_002373.6(MAP1A):c.7916G>A (p.Arg2639Gln)	not specified [RCV004335474]	uncertain significance	15	43529389	43529389	Human		name
401895865	CV2769096	single nucleotide variant	NM_002373.6(MAP1A):c.4798T>C (p.Ser1600Pro)	not specified [RCV004348953]	uncertain significance	15	43526271	43526271	Human		name
401882121	CV2784076	single nucleotide variant	NM_002373.6(MAP1A):c.7060T>G (p.Ser2354Ala)	not specified [RCV004362476]	uncertain significance	15	43528533	43528533	Human		name
401884868	CV2786602	single nucleotide variant	NM_002373.6(MAP1A):c.6088A>G (p.Thr2030Ala)	not specified [RCV004363742]	uncertain significance	15	43527561	43527561	Human		name
401908286	CV2801326	single nucleotide variant	NM_002373.6(MAP1A):c.6902G>A (p.Trp2301Ter)	MAP1A-related disorder [RCV003397567]	uncertain significance	15	43528375	43528375	Human		name , trait , alternate_id
401913537	CV2801816	single nucleotide variant	NM_002373.6(MAP1A):c.7840A>C (p.Lys2614Gln)	MAP1A-related disorder [RCV003400159]	uncertain significance	15	43529313	43529313	Human		name , trait , alternate_id
401906129	CV2802456	single nucleotide variant	NM_002373.6(MAP1A):c.8201G>A (p.Arg2734Gln)	MAP1A-related disorder [RCV003421071]\|not specified [RCV004935328]	uncertain significance	15	43529815	43529815	Human		name , trait , alternate_id
405263720	CV3189786	single nucleotide variant	NM_002373.6(MAP1A):c.6170T>G (p.Leu2057Arg)	MAP1A-related disorder [RCV003896835]	uncertain significance	15	43527643	43527643	Human		name , trait , alternate_id
405282551	CV3191086	single nucleotide variant	NM_002373.6(MAP1A):c.6226C>T (p.Pro2076Ser)	MAP1A-related disorder [RCV003921503]	uncertain significance	15	43527699	43527699	Human		name , trait , alternate_id
405283168	CV3191268	single nucleotide variant	NM_002373.6(MAP1A):c.7721G>A (p.Arg2574His)	MAP1A-related disorder [RCV003921672]	likely benign	15	43529194	43529194	Human		name , trait , alternate_id
405266693	CV3202065	single nucleotide variant	NM_002373.6(MAP1A):c.7570T>A (p.Ser2524Thr)	MAP1A-related disorder [RCV003911546]\|not specified [RCV004636880]	uncertain significance	15	43529043	43529043	Human		name , trait , alternate_id
405267772	CV3205681	single nucleotide variant	NM_002373.6(MAP1A):c.6602C>T (p.Ala2201Val)	MAP1A-related disorder [RCV003947404]	uncertain significance	15	43528075	43528075	Human		name , trait , alternate_id
405270577	CV3211471	single nucleotide variant	NM_002373.6(MAP1A):c.3234C>G (p.Asn1078Lys)	MAP1A-related disorder [RCV003949355]	likely benign	15	43524707	43524707	Human		name , trait , alternate_id
405657162	CV3288458	single nucleotide variant	NM_002373.6(MAP1A):c.3581C>A (p.Thr1194Asn)	not specified [RCV004416054]	uncertain significance	15	43525054	43525054	Human		name
405657166	CV3288459	single nucleotide variant	NM_002373.6(MAP1A):c.3653C>T (p.Ser1218Phe)	not specified [RCV004416055]	uncertain significance	15	43525126	43525126	Human		name
405657169	CV3288460	single nucleotide variant	NM_002373.6(MAP1A):c.3658G>A (p.Glu1220Lys)	not specified [RCV004416056]	uncertain significance	15	43525131	43525131	Human		name
405657173	CV3288461	single nucleotide variant	NM_002373.6(MAP1A):c.3815G>A (p.Arg1272Gln)	not specified [RCV004416057]	uncertain significance	15	43525288	43525288	Human		name
405657177	CV3288462	single nucleotide variant	NM_002373.6(MAP1A):c.3868G>T (p.Ala1290Ser)	not specified [RCV004416058]	uncertain significance	15	43525341	43525341	Human		name
405657184	CV3288464	single nucleotide variant	NM_002373.6(MAP1A):c.3920G>A (p.Gly1307Glu)	not specified [RCV004416060]	uncertain significance	15	43525393	43525393	Human		name
405657188	CV3288465	single nucleotide variant	NM_002373.6(MAP1A):c.4085C>T (p.Pro1362Leu)	not specified [RCV004416061]	uncertain significance	15	43525558	43525558	Human		name
405657191	CV3288466	single nucleotide variant	NM_002373.6(MAP1A):c.4393G>C (p.Glu1465Gln)	not specified [RCV004416062]	uncertain significance	15	43525866	43525866	Human		name
405657194	CV3288467	single nucleotide variant	NM_002373.6(MAP1A):c.4622A>G (p.Asp1541Gly)	not specified [RCV004416063]	uncertain significance	15	43526095	43526095	Human		name
405657197	CV3288468	single nucleotide variant	NM_002373.6(MAP1A):c.4897G>A (p.Ala1633Thr)	not specified [RCV004416064]	uncertain significance	15	43526370	43526370	Human		name
405657200	CV3288469	single nucleotide variant	NM_002373.6(MAP1A):c.5492A>G (p.Asn1831Ser)	not specified [RCV004416065]	uncertain significance	15	43526965	43526965	Human		name
405657204	CV3288470	single nucleotide variant	NM_002373.6(MAP1A):c.5714T>G (p.Leu1905Arg)	not specified [RCV004416066]	uncertain significance	15	43527187	43527187	Human		name
405657206	CV3288471	single nucleotide variant	NM_002373.6(MAP1A):c.5756A>G (p.Glu1919Gly)	not specified [RCV004416067]	uncertain significance	15	43527229	43527229	Human		name
405657209	CV3288472	single nucleotide variant	NM_002373.6(MAP1A):c.5759G>A (p.Gly1920Asp)	not specified [RCV004416068]	uncertain significance	15	43527232	43527232	Human		name
405657214	CV3288473	single nucleotide variant	NM_002373.6(MAP1A):c.5773C>G (p.Pro1925Ala)	not specified [RCV004416069]	uncertain significance	15	43527246	43527246	Human		name
405657216	CV3288474	single nucleotide variant	NM_002373.6(MAP1A):c.5941C>T (p.Pro1981Ser)	not specified [RCV004416070]	uncertain significance	15	43527414	43527414	Human		name
405657219	CV3288475	single nucleotide variant	NM_002373.6(MAP1A):c.6022G>A (p.Gly2008Ser)	not specified [RCV004416071]	uncertain significance	15	43527495	43527495	Human		name
405657223	CV3288476	single nucleotide variant	NM_002373.6(MAP1A):c.6110C>A (p.Ala2037Asp)	not specified [RCV004416072]	uncertain significance	15	43527583	43527583	Human		name
405657227	CV3288477	single nucleotide variant	NM_002373.6(MAP1A):c.6151C>T (p.Pro2051Ser)	not specified [RCV004416073]	uncertain significance	15	43527624	43527624	Human		name
405657230	CV3288478	single nucleotide variant	NM_002373.6(MAP1A):c.6344G>T (p.Arg2115Leu)	not specified [RCV004416074]	uncertain significance	15	43527817	43527817	Human		name
405657233	CV3288479	single nucleotide variant	NM_002373.6(MAP1A):c.6559C>T (p.Arg2187Cys)	not specified [RCV004416075]	uncertain significance	15	43528032	43528032	Human		name
405657237	CV3288480	single nucleotide variant	NM_002373.6(MAP1A):c.6758C>T (p.Pro2253Leu)	not specified [RCV004416076]	uncertain significance	15	43528231	43528231	Human		name
405657239	CV3288481	single nucleotide variant	NM_002373.6(MAP1A):c.6791C>T (p.Thr2264Ile)	not specified [RCV004416077]	uncertain significance	15	43528264	43528264	Human		name
405657244	CV3288482	single nucleotide variant	NM_002373.6(MAP1A):c.7054G>C (p.Val2352Leu)	not specified [RCV004416078]	uncertain significance	15	43528527	43528527	Human		name
405657247	CV3288483	single nucleotide variant	NM_002373.6(MAP1A):c.7435C>T (p.Arg2479Trp)	not specified [RCV004416079]	uncertain significance	15	43528908	43528908	Human		name
405657249	CV3288484	single nucleotide variant	NM_002373.6(MAP1A):c.7441C>T (p.Arg2481Trp)	not specified [RCV004416080]	uncertain significance	15	43528914	43528914	Human		name
405657252	CV3288485	single nucleotide variant	NM_002373.6(MAP1A):c.7580C>T (p.Ala2527Val)	not specified [RCV004416081]	uncertain significance	15	43529053	43529053	Human		name
407493497	CV3446364	single nucleotide variant	NM_002373.6(MAP1A):c.6182C>T (p.Ala2061Val)	not specified [RCV004642750]	uncertain significance	15	43527655	43527655	Human		name
407493502	CV3446365	single nucleotide variant	NM_002373.6(MAP1A):c.5227C>T (p.Arg1743Trp)	not specified [RCV004642751]	uncertain significance	15	43526700	43526700	Human		name
407493512	CV3446367	single nucleotide variant	NM_002373.6(MAP1A):c.5109G>C (p.Glu1703Asp)	not specified [RCV004642753]	uncertain significance	15	43526582	43526582	Human		name
407468930	CV3446369	single nucleotide variant	NM_002373.6(MAP1A):c.7169G>A (p.Arg2390His)	not specified [RCV004636452]	uncertain significance	15	43528642	43528642	Human		name
407493526	CV3446371	single nucleotide variant	NM_002373.6(MAP1A):c.5486T>C (p.Met1829Thr)	not specified [RCV004642756]	uncertain significance	15	43526959	43526959	Human		name
407468932	CV3446374	single nucleotide variant	NM_002373.6(MAP1A):c.7229A>T (p.Glu2410Val)	not specified [RCV004636453]	uncertain significance	15	43528702	43528702	Human		name
407493535	CV3446375	single nucleotide variant	NM_002373.6(MAP1A):c.7304A>G (p.Gln2435Arg)	not specified [RCV004642759]	uncertain significance	15	43528777	43528777	Human		name
407493539	CV3446376	single nucleotide variant	NM_002373.6(MAP1A):c.4639A>G (p.Lys1547Glu)	not specified [RCV004642760]	uncertain significance	15	43526112	43526112	Human		name
407493545	CV3446377	single nucleotide variant	NM_002373.6(MAP1A):c.4517T>C (p.Val1506Ala)	not specified [RCV004642761]	uncertain significance	15	43525990	43525990	Human		name
407493549	CV3446378	single nucleotide variant	NM_002373.6(MAP1A):c.5205T>G (p.Asp1735Glu)	not specified [RCV004642762]	uncertain significance	15	43526678	43526678	Human		name
407468936	CV3446379	single nucleotide variant	NM_002373.6(MAP1A):c.5110C>T (p.Arg1704Trp)	not specified [RCV004636454]	uncertain significance	15	43526583	43526583	Human		name
407493556	CV3446380	single nucleotide variant	NM_002373.6(MAP1A):c.7646G>A (p.Ser2549Asn)	not specified [RCV004642763]	uncertain significance	15	43529119	43529119	Human		name
407468940	CV3446381	single nucleotide variant	NM_002373.6(MAP1A):c.5174G>A (p.Arg1725Gln)	not specified [RCV004636455]	uncertain significance	15	43526647	43526647	Human		name
407493561	CV3446382	single nucleotide variant	NM_002373.6(MAP1A):c.6337G>C (p.Gly2113Arg)	not specified [RCV004642764]	uncertain significance	15	43527810	43527810	Human		name
407493572	CV3446385	single nucleotide variant	NM_002373.6(MAP1A):c.6320A>G (p.Asp2107Gly)	not specified [RCV004642767]	uncertain significance	15	43527793	43527793	Human		name
597626767	CV3702847	single nucleotide variant	NM_002373.6(MAP1A):c.4532C>T (p.Pro1511Leu)	not specified [RCV004938625]	uncertain significance	15	43526005	43526005	Human		name
597626762	CV3702849	single nucleotide variant	NM_002373.6(MAP1A):c.7261G>A (p.Gly2421Ser)	not specified [RCV004938627]	uncertain significance	15	43528734	43528734	Human		name
597626758	CV3702850	single nucleotide variant	NM_002373.6(MAP1A):c.5938G>A (p.Gly1980Ser)	not specified [RCV004938628]	uncertain significance	15	43527411	43527411	Human		name
597626754	CV3702851	single nucleotide variant	NM_002373.6(MAP1A):c.5288C>G (p.Pro1763Arg)	not specified [RCV004938629]	uncertain significance	15	43526761	43526761	Human		name
597626750	CV3702852	single nucleotide variant	NM_002373.6(MAP1A):c.5312G>A (p.Arg1771His)	not specified [RCV004938630]	uncertain significance	15	43526785	43526785	Human		name
597626744	CV3702854	single nucleotide variant	NM_002373.6(MAP1A):c.7942C>T (p.Arg2648Cys)	not specified [RCV004938632]	uncertain significance	15	43529415	43529415	Human		name
597626740	CV3702855	single nucleotide variant	NM_002373.6(MAP1A):c.4681A>G (p.Lys1561Glu)	not specified [RCV004938633]	uncertain significance	15	43526154	43526154	Human		name
597626737	CV3702856	single nucleotide variant	NM_002373.6(MAP1A):c.7859G>A (p.Arg2620Gln)	not specified [RCV004938634]	uncertain significance	15	43529332	43529332	Human		name
597626725	CV3702860	single nucleotide variant	NM_002373.6(MAP1A):c.6494C>T (p.Ala2165Val)	not specified [RCV004938638]	uncertain significance	15	43527967	43527967	Human		name
597626722	CV3702862	single nucleotide variant	NM_002373.6(MAP1A):c.6292C>T (p.Arg2098Trp)	not specified [RCV004938639]	uncertain significance	15	43527765	43527765	Human		name
597626604	CV3702863	single nucleotide variant	NM_002373.6(MAP1A):c.5279A>C (p.Glu1760Ala)	not specified [RCV004938640]	uncertain significance	15	43526752	43526752	Human		name
597626447	CV3702865	single nucleotide variant	NM_002373.6(MAP1A):c.7031C>T (p.Thr2344Met)	not specified [RCV004938642]	uncertain significance	15	43528504	43528504	Human		name
597626389	CV3702866	single nucleotide variant	NM_002373.6(MAP1A):c.7204C>T (p.Arg2402Trp)	not specified [RCV004938643]	uncertain significance	15	43528677	43528677	Human		name
597626392	CV3702867	single nucleotide variant	NM_002373.6(MAP1A):c.6529C>T (p.Pro2177Ser)	not specified [RCV004938644]	uncertain significance	15	43528002	43528002	Human		name
597626400	CV3702869	single nucleotide variant	NM_002373.6(MAP1A):c.3896C>T (p.Ser1299Leu)	not specified [RCV004938646]	likely benign	15	43525369	43525369	Human		name
597626404	CV3702870	single nucleotide variant	NM_002373.6(MAP1A):c.3730G>A (p.Glu1244Lys)	not specified [RCV004938647]	uncertain significance	15	43525203	43525203	Human		name
597626408	CV3702871	single nucleotide variant	NM_002373.6(MAP1A):c.8141G>A (p.Arg2714Gln)	not specified [RCV004938648]	uncertain significance	15	43529755	43529755	Human		name
597626415	CV3702873	single nucleotide variant	NM_002373.6(MAP1A):c.7946G>A (p.Ser2649Asn)	not specified [RCV004938650]	uncertain significance	15	43529419	43529419	Human		name
597626417	CV3702874	single nucleotide variant	NM_002373.6(MAP1A):c.3439C>T (p.Pro1147Ser)	not specified [RCV004938651]	uncertain significance	15	43524912	43524912	Human		name
597626420	CV3702875	single nucleotide variant	NM_002373.6(MAP1A):c.5277G>C (p.Gln1759His)	not specified [RCV004938652]	uncertain significance	15	43526750	43526750	Human		name
597626424	CV3702876	single nucleotide variant	NM_002373.6(MAP1A):c.4730A>G (p.Gln1577Arg)	not specified [RCV004938653]	uncertain significance	15	43526203	43526203	Human		name
597626427	CV3702877	single nucleotide variant	NM_002373.6(MAP1A):c.3409G>A (p.Val1137Met)	not specified [RCV004938654]	uncertain significance	15	43524882	43524882	Human		name
597626431	CV3702878	single nucleotide variant	NM_002373.6(MAP1A):c.5947T>C (p.Cys1983Arg)	not specified [RCV004938655]	uncertain significance	15	43527420	43527420	Human		name
597626434	CV3702879	single nucleotide variant	NM_002373.6(MAP1A):c.4897G>T (p.Ala1633Ser)	not specified [RCV004938656]	uncertain significance	15	43526370	43526370	Human		name
597626437	CV3702881	single nucleotide variant	NM_002373.6(MAP1A):c.5510C>T (p.Ser1837Leu)	not specified [RCV004938657]	uncertain significance	15	43526983	43526983	Human		name
597626444	CV3702883	single nucleotide variant	NM_002373.6(MAP1A):c.7366C>T (p.Pro2456Ser)	not specified [RCV004938659]	uncertain significance	15	43528839	43528839	Human		name
597626791	CV3702884	single nucleotide variant	NM_002373.6(MAP1A):c.4151A>T (p.Asp1384Val)	not specified [RCV004938660]	uncertain significance	15	43525624	43525624	Human		name
597626451	CV3702885	single nucleotide variant	NM_002373.6(MAP1A):c.3763G>T (p.Val1255Phe)	not specified [RCV004938661]	uncertain significance	15	43525236	43525236	Human		name
597626461	CV3702888	single nucleotide variant	NM_002373.6(MAP1A):c.3104G>T (p.Arg1035Leu)	not specified [RCV004938664]	uncertain significance	15	43524577	43524577	Human		name
597626465	CV3702889	single nucleotide variant	NM_002373.6(MAP1A):c.7115C>T (p.Pro2372Leu)	not specified [RCV004938665]	uncertain significance	15	43528588	43528588	Human		name
597626468	CV3702890	single nucleotide variant	NM_002373.6(MAP1A):c.6931C>T (p.Pro2311Ser)	not specified [RCV004938666]	uncertain significance	15	43528404	43528404	Human		name
597626472	CV3702892	single nucleotide variant	NM_002373.6(MAP1A):c.3568T>C (p.Ser1190Pro)	not specified [RCV004938667]	uncertain significance	15	43525041	43525041	Human		name
597626479	CV3702894	single nucleotide variant	NM_002373.6(MAP1A):c.3590T>C (p.Leu1197Pro)	not specified [RCV004938669]	uncertain significance	15	43525063	43525063	Human		name
598122565	CV3884496	single nucleotide variant	NM_002373.6(MAP1A):c.4330G>T (p.Glu1444Ter)	not specified [RCV005237188]	uncertain significance	15	43525803	43525803	Human		name
598165879	CV3988526	single nucleotide variant	NM_002373.6(MAP1A):c.6821G>A (p.Arg2274His)	not specified [RCV005369244]	uncertain significance	15	43528294	43528294	Human		name
598196440	CV3988527	single nucleotide variant	NM_002373.6(MAP1A):c.6191C>G (p.Pro2064Arg)	not specified [RCV005375268]	uncertain significance	15	43527664	43527664	Human		name
598196447	CV3988529	single nucleotide variant	NM_002373.6(MAP1A):c.3472G>A (p.Val1158Met)	not specified [RCV005375269]	uncertain significance	15	43524945	43524945	Human		name
598196454	CV3988530	single nucleotide variant	NM_002373.6(MAP1A):c.6059C>T (p.Pro2020Leu)	not specified [RCV005375270]	uncertain significance	15	43527532	43527532	Human		name
598165893	CV3988531	single nucleotide variant	NM_002373.6(MAP1A):c.7924C>T (p.Arg2642Trp)	not specified [RCV005369246]	uncertain significance	15	43529397	43529397	Human		name
598196461	CV3988532	single nucleotide variant	NM_002373.6(MAP1A):c.8291C>G (p.Thr2764Ser)	not specified [RCV005375271]	uncertain significance	15	43530103	43530103	Human		name
598165901	CV3988535	single nucleotide variant	NM_002373.6(MAP1A):c.6415T>C (p.Trp2139Arg)	not specified [RCV005369247]	uncertain significance	15	43527888	43527888	Human		name
598196478	CV3988536	single nucleotide variant	NM_002373.6(MAP1A):c.7349C>T (p.Pro2450Leu)	not specified [RCV005375274]	uncertain significance	15	43528822	43528822	Human		name
598165910	CV3988539	single nucleotide variant	NM_002373.6(MAP1A):c.7674T>G (p.His2558Gln)	not specified [RCV005369248]	uncertain significance	15	43529147	43529147	Human		name
598196496	CV3988540	single nucleotide variant	NM_002373.6(MAP1A):c.6157A>G (p.Met2053Val)	not specified [RCV005375277]	likely benign	15	43527630	43527630	Human		name
598196503	CV3988541	single nucleotide variant	NM_002373.6(MAP1A):c.6989A>G (p.Asp2330Gly)	not specified [RCV005375278]	uncertain significance	15	43528462	43528462	Human		name
598165916	CV3988542	single nucleotide variant	NM_002373.6(MAP1A):c.5929A>G (p.Thr1977Ala)	not specified [RCV005369249]	uncertain significance	15	43527402	43527402	Human		name
598196509	CV3988543	single nucleotide variant	NM_002373.6(MAP1A):c.3238G>A (p.Asp1080Asn)	not specified [RCV005375279]	uncertain significance	15	43524711	43524711	Human		name
598196516	CV3988544	single nucleotide variant	NM_002373.6(MAP1A):c.8336A>G (p.Asn2779Ser)	not specified [RCV005375280]	uncertain significance	15	43530148	43530148	Human		name
598196522	CV3988546	single nucleotide variant	NM_002373.6(MAP1A):c.3007C>T (p.Pro1003Ser)	not specified [RCV005375281]	uncertain significance	15	43524480	43524480	Human		name
598196528	CV3988547	single nucleotide variant	NM_002373.6(MAP1A):c.6204C>G (p.Ile2068Met)	not specified [RCV005375282]	uncertain significance	15	43527677	43527677	Human		name
598196535	CV3988548	single nucleotide variant	NM_002373.6(MAP1A):c.7006C>T (p.His2336Tyr)	not specified [RCV005375283]	uncertain significance	15	43528479	43528479	Human		name
598165927	CV3988549	single nucleotide variant	NM_002373.6(MAP1A):c.7331A>G (p.His2444Arg)	not specified [RCV005369251]	uncertain significance	15	43528804	43528804	Human		name
598165932	CV3988550	single nucleotide variant	NM_002373.6(MAP1A):c.3763G>C (p.Val1255Leu)	not specified [RCV005369252]	uncertain significance	15	43525236	43525236	Human		name
598196554	CV3988554	single nucleotide variant	NM_002373.6(MAP1A):c.5857C>G (p.Gln1953Glu)	not specified [RCV005375286]	uncertain significance	15	43527330	43527330	Human		name
598165942	CV3988556	single nucleotide variant	NM_002373.6(MAP1A):c.3416G>C (p.Arg1139Thr)	not specified [RCV005369254]	uncertain significance	15	43524889	43524889	Human		name
15102046	CV703221	single nucleotide variant	NM_002373.6(MAP1A):c.4861C>G (p.Leu1621Val)	not provided [RCV000959215]	benign	15	43526334	43526334	Human		name
15101692	CV703222	single nucleotide variant	NM_002373.6(MAP1A):c.5573C>G (p.Ser1858Cys)	not provided [RCV000959142]	likely benign	15	43527046	43527046	Human		name
8627641	CV82785	single nucleotide variant	NM_002373.5(MAP1A):c.4778C>T (p.Pro1593Leu)	Malignant melanoma [RCV000062865]	not provided	15	43526251	43526251	Human		name
38463977	CV961323	single nucleotide variant	NM_002373.6(MAP1A):c.3571C>G (p.Pro1191Ala)	not provided [RCV001249398]	not provided	15	43525044	43525044	Human		name
152983111	CV1677950	microsatellite	NM_002373.6(MAP1A):c.5484_5485del (p.Met1829fs)	Neurodevelopmental disorder [RCV002250104]	pathogenic	15	43526953	43526954	Human		name
401927333	CV2796851	deletion	NM_002373.6(MAP1A):c.6656_6667del (p.Glu2219_Lys2222del)	MAP1A-related disorder [RCV003406139]	uncertain significance	15	43528127	43528138	Human		name , trait , alternate_id

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