Nat1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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189 records found for search term Nat1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8566397	CV32846	variation	NAT1*10 ALLELE	NAT1*10 ALLELE [RCV000019385]	pathogenic\|other				Human		name , trait
597655762	CV3565232	single nucleotide variant	NM_000662.8(NAT1):c.88C>A (p.His30Asn)	not specified [RCV004834133]	uncertain significance	8	18222135	18222135	Human		name
329363982	CV2469596	single nucleotide variant	NM_000662.8(NAT1):c.117C>G (p.Asn39Lys)	not specified [RCV004283027]	uncertain significance	8	18222164	18222164	Human		name
11525970	CV247031	single nucleotide variant	NM_000662.8(NAT1):c.190C>T (p.Arg64Trp)	not specified [RCV000239134]	benign	8	18222237	18222237	Human	1	name
11525970	CV247031	single nucleotide variant	NM_000662.8(NAT1):c.190C>T (p.Arg64Trp)	not specified [RCV000239134]	benign	8	18222237	18222238	Human	1	name
597655754	CV3565233	single nucleotide variant	NM_000662.8(NAT1):c.256A>G (p.Thr86Ala)	not specified [RCV004834134]	uncertain significance	8	18222303	18222303	Human		name
597655746	CV3565234	single nucleotide variant	NM_000662.8(NAT1):c.277G>C (p.Val93Leu)	not specified [RCV004834135]	uncertain significance	8	18222324	18222324	Human		name
598215341	CV3983347	single nucleotide variant	NM_000662.8(NAT1):c.178G>C (p.Val60Leu)	not specified [RCV005378734]	uncertain significance	8	18222225	18222225	Human		name
598215353	CV3983349	single nucleotide variant	NM_000662.8(NAT1):c.245T>A (p.Ile82Asn)	not specified [RCV005378736]	uncertain significance	8	18222292	18222292	Human		name
156397838	CV2193796	single nucleotide variant	NM_000662.8(NAT1):c.386A>T (p.Tyr129Phe)	not specified [RCV004074550]	uncertain significance	8	18222433	18222433	Human		name
155976031	CV2270138	single nucleotide variant	NM_000662.8(NAT1):c.810A>G (p.Ile270Met)	not specified [RCV004129085]	uncertain significance	8	18222857	18222857	Human		name
155906606	CV2379076	single nucleotide variant	NM_000662.8(NAT1):c.504G>T (p.Gln168His)	not specified [RCV004233832]	uncertain significance	8	18222551	18222551	Human		name
329371552	CV2458897	single nucleotide variant	NM_000662.8(NAT1):c.589C>G (p.Arg197Gly)	not specified [RCV004270306]	uncertain significance	8	18222636	18222636	Human		name
401865779	CV2755634	single nucleotide variant	NM_000662.8(NAT1):c.380G>A (p.Arg127His)	not specified [RCV004342020]	uncertain significance	8	18222427	18222427	Human		name
401892490	CV2782078	single nucleotide variant	NM_000662.8(NAT1):c.505T>A (p.Tyr169Asn)	not specified [RCV004359074]	uncertain significance	8	18222552	18222552	Human		name
405768269	CV3324944	single nucleotide variant	NM_000662.8(NAT1):c.535G>A (p.Asp179Asn)	not specified [RCV004469834]	uncertain significance	8	18222582	18222582	Human		name
405780773	CV3324956	single nucleotide variant	NM_000662.8(NAT1):c.808A>G (p.Ile270Val)	not specified [RCV004471913]	uncertain significance	8	18222855	18222855	Human		name
407520788	CV3447963	single nucleotide variant	NM_000662.8(NAT1):c.359T>C (p.Ile120Thr)	not specified [RCV004652304]	uncertain significance	8	18222406	18222406	Human		name
598159355	CV3983346	single nucleotide variant	NM_000662.8(NAT1):c.784G>C (p.Glu262Gln)	not specified [RCV005390140]	uncertain significance	8	18222831	18222831	Human		name
598215346	CV3983348	single nucleotide variant	NM_000662.8(NAT1):c.815A>G (p.Asn272Ser)	not specified [RCV005378735]	uncertain significance	8	18222862	18222862	Human		name
15178313	CV722974	single nucleotide variant	NM_000662.8(NAT1):c.315G>T (p.Met105Ile)	not provided [RCV000885033]	likely benign	8	18222362	18222362	Human		name
8566398	CV32847	single nucleotide variant	NM_001160179.2(NAT1):c.445G>A (p.Val149Ile)	NAT1*17 ALLELE [RCV000019386]\|not provided [RCV004712000]\|not specified [RCV000455973]	pathogenic\|benign\|other	8	18222492	18222492	Human		name , trait
8634026	CV89244	single nucleotide variant	NAT10:c.1077C>T	Malignant melanoma [RCV000069341]	not provided	11	34130861	34130861	Human		name
15180898	CV779541	single nucleotide variant	NM_024662.3(NAT10):c.373-7C>T	not provided [RCV000974262]	benign	11	34113709	34113709	Human		name
15189976	CV730764	single nucleotide variant	NM_024662.3(NAT10):c.2885+6G>C	not provided [RCV000887973]	benign	11	34142354	34142354	Human		name
156376792	CV2206843	single nucleotide variant	NM_024662.3(NAT10):c.7C>T (p.Arg3Trp)	not specified [RCV004083517]	uncertain significance	11	34108232	34108232	Human		name
405782042	CV3342452	single nucleotide variant	NM_020378.4(NAT14):c.8C>T (p.Pro3Leu)	not specified [RCV004472128]	uncertain significance	19	55485716	55485716	Human		name
598215402	CV3983364	single nucleotide variant	NM_020378.4(NAT14):c.7C>T (p.Pro3Ser)	not specified [RCV005378746]	uncertain significance	19	55485715	55485715	Human		name
155990499	CV2285268	single nucleotide variant	NM_198571.3(NAT16):c.14C>A (p.Ala5Asp)	not specified [RCV004145461]	uncertain significance	7	101174794	101174794	Human		name
405781785	CV3325128	single nucleotide variant	NM_020378.4(NAT14):c.11G>A (p.Ser4Asn)	not specified [RCV004472085]	uncertain significance	19	55485719	55485719	Human		name
598215429	CV3983370	single nucleotide variant	NM_198571.3(NAT16):c.10G>A (p.Glu4Lys)	not specified [RCV005378751]	uncertain significance	7	101174798	101174798	Human		name
15172958	CV724406	single nucleotide variant	NM_024662.3(NAT10):c.177T>C (p.Tyr59=)	not provided [RCV000883945]	benign	11	34108810	34108810	Human		name
15180853	CV737950	single nucleotide variant	NM_024662.3(NAT10):c.273C>T (p.Asp91=)	not provided [RCV000907452]	likely benign	11	34112124	34112124	Human		name
156157594	CV2262413	single nucleotide variant	NM_020378.4(NAT14):c.40G>A (p.Asp14Asn)	not specified [RCV004128859]	uncertain significance	19	55485748	55485748	Human		name
155994456	CV2377517	single nucleotide variant	NM_024662.3(NAT10):c.37C>T (p.Leu13Phe)	not specified [RCV004225676]	uncertain significance	11	34108262	34108262	Human		name
155999933	CV2396504	single nucleotide variant	NM_198571.3(NAT16):c.50C>T (p.Pro17Leu)	not specified [RCV004242214]	uncertain significance	7	101174758	101174758	Human		name
329357047	CV2460672	single nucleotide variant	NM_198571.3(NAT16):c.74C>G (p.Ala25Gly)	not specified [RCV004270713]	uncertain significance	7	101174734	101174734	Human		name
401736955	CV2679190	single nucleotide variant	NM_024662.3(NAT10):c.89G>A (p.Gly30Glu)	not specified [RCV004285749]	uncertain significance	11	34108314	34108314	Human		name
405782301	CV3342497	single nucleotide variant	NM_198571.3(NAT16):c.47A>G (p.Lys16Arg)	not specified [RCV004472173]	uncertain significance	7	101174761	101174761	Human		name
405782403	CV3342515	single nucleotide variant	NM_198571.3(NAT16):c.61A>G (p.Thr21Ala)	not specified [RCV004472191]	likely benign	7	101174747	101174747	Human		name
598215386	CV3983361	single nucleotide variant	NM_020378.4(NAT14):c.76G>C (p.Gly26Arg)	not specified [RCV005378743]	uncertain significance	19	55486411	55486411	Human		name
15180901	CV712796	single nucleotide variant	NM_024662.3(NAT10):c.459C>T (p.Thr153=)	not provided [RCV000974263]	benign	11	34113802	34113802	Human		name
15151774	CV712797	single nucleotide variant	NM_024662.3(NAT10):c.609G>A (p.Gln203=)	not provided [RCV000968212]	benign	11	34118231	34118231	Human		name
15172963	CV724407	single nucleotide variant	NM_024662.3(NAT10):c.369G>A (p.Leu123=)	not provided [RCV000883946]	benign	11	34112220	34112220	Human		name
156088024	CV2259021	single nucleotide variant	NM_198571.3(NAT16):c.215G>T (p.Gly72Val)	not specified [RCV004120287]	uncertain significance	7	101174593	101174593	Human		name
156168483	CV2337296	single nucleotide variant	NM_198571.3(NAT16):c.271C>A (p.Pro91Thr)	not specified [RCV004187749]	uncertain significance	7	101174537	101174537	Human		name
401728305	CV2672868	single nucleotide variant	NM_198571.3(NAT16):c.211G>C (p.Gly71Arg)	not specified [RCV004282039]	uncertain significance	7	101174597	101174597	Human		name
401737542	CV2695828	single nucleotide variant	NM_198571.3(NAT16):c.131C>T (p.Ser44Leu)	not specified [RCV004308111]	uncertain significance	7	101174677	101174677	Human		name
401884783	CV2766241	single nucleotide variant	NM_020378.4(NAT14):c.160G>A (p.Gly54Ser)	not specified [RCV004340677]	uncertain significance	19	55486495	55486495	Human		name
401866158	CV2775440	single nucleotide variant	NM_198571.3(NAT16):c.119C>G (p.Pro40Arg)	not specified [RCV004348836]	uncertain significance	7	101174689	101174689	Human		name
401894266	CV2780527	single nucleotide variant	NM_020378.4(NAT14):c.172G>T (p.Val58Phe)	not specified [RCV004358215]	uncertain significance	19	55486507	55486507	Human		name
401896447	CV2781394	single nucleotide variant	NM_024662.3(NAT10):c.287T>C (p.Phe96Ser)	not specified [RCV004352398]	uncertain significance	11	34112138	34112138	Human		name
407520797	CV3447973	single nucleotide variant	NM_024662.3(NAT10):c.134C>T (p.Ser45Phe)	not specified [RCV004652307]	uncertain significance	11	34108767	34108767	Human		name
407520800	CV3458073	single nucleotide variant	NM_020378.4(NAT14):c.113C>A (p.Ala38Asp)	not specified [RCV004652308]	uncertain significance	19	55486448	55486448	Human		name
597654897	CV3565249	single nucleotide variant	NM_020378.4(NAT14):c.211T>G (p.Phe71Val)	not specified [RCV004834150]	uncertain significance	19	55486546	55486546	Human		name
597654915	CV3565251	single nucleotide variant	NM_198571.3(NAT16):c.106G>A (p.Val36Met)	not specified [RCV004834152]	uncertain significance	7	101174702	101174702	Human		name
597655949	CV3565256	single nucleotide variant	NM_198571.3(NAT16):c.255C>G (p.His85Gln)	not specified [RCV004834157]	uncertain significance	7	101174553	101174553	Human		name
12895976	CV390041	single nucleotide variant	NM_024662.3(NAT10):c.1686C>T (p.Pro562=)	not provided [RCV004718677]\|not specified [RCV000454708]	benign	11	34133094	34133094	Human		name
598215368	CV3983354	single nucleotide variant	NM_024662.3(NAT10):c.204C>A (p.His68Gln)	not specified [RCV005378739]	uncertain significance	11	34112055	34112055	Human		name
598215377	CV3983358	single nucleotide variant	NM_024662.3(NAT10):c.115A>G (p.Ile39Val)	not specified [RCV005378741]	uncertain significance	11	34108748	34108748	Human		name
598215391	CV3983362	single nucleotide variant	NM_020378.4(NAT14):c.211T>A (p.Phe71Ile)	not specified [RCV005378744]	uncertain significance	19	55486546	55486546	Human		name
598252264	CV3983366	single nucleotide variant	NM_198571.3(NAT16):c.215G>A (p.Gly72Asp)	not specified [RCV005385133]	uncertain significance	7	101174593	101174593	Human		name
598215413	CV3983367	single nucleotide variant	NM_198571.3(NAT16):c.178G>C (p.Glu60Gln)	not specified [RCV005378748]	uncertain significance	7	101174630	101174630	Human		name
598215424	CV3983369	single nucleotide variant	NM_198571.3(NAT16):c.147G>C (p.Glu49Asp)	not specified [RCV005378750]	uncertain significance	7	101174661	101174661	Human		name
8689403	CV97491	single nucleotide variant	NM_024662.3(NAT10):c.2424G>C (p.Leu808=)	not provided [RCV000122570]	uncertain significance	11	34140404	34140404	Human		name
151662492	CV1333148	single nucleotide variant	NM_024662.3(NAT10):c.394A>G (p.Asn132Asp)	not provided [RCV004799673]\|not specified [RCV004041028]	uncertain significance	11	34113737	34113737	Human		name
156314781	CV2196693	single nucleotide variant	NM_024662.3(NAT10):c.685G>C (p.Gly229Arg)	not specified [RCV004073952]	uncertain significance	11	34118408	34118408	Human		name
155901083	CV2241907	single nucleotide variant	NM_198571.3(NAT16):c.811C>T (p.Arg271Cys)	not specified [RCV004106818]	uncertain significance	7	101172378	101172378	Human		name
156035203	CV2253016	single nucleotide variant	NM_198571.3(NAT16):c.608G>A (p.Arg203Gln)	not specified [RCV004120813]	uncertain significance	7	101172581	101172581	Human		name
156090598	CV2256519	single nucleotide variant	NM_024662.3(NAT10):c.317A>G (p.Tyr106Cys)	not specified [RCV004118722]	uncertain significance	11	34112168	34112168	Human		name
156008943	CV2294288	single nucleotide variant	NM_198571.3(NAT16):c.521G>A (p.Arg174His)	not specified [RCV004151419]	uncertain significance	7	101173312	101173312	Human		name
155956194	CV2304001	single nucleotide variant	NM_020378.4(NAT14):c.517G>A (p.Ala173Thr)	not specified [RCV004170056]	uncertain significance	19	55486852	55486852	Human		name
156283390	CV2317461	single nucleotide variant	NM_024662.3(NAT10):c.365T>C (p.Val122Ala)	not specified [RCV004172426]	uncertain significance	11	34112216	34112216	Human		name
156395807	CV2325937	single nucleotide variant	NM_024662.3(NAT10):c.989T>C (p.Phe330Ser)	not specified [RCV004174109]	uncertain significance	11	34123836	34123836	Human		name
156359734	CV2328286	single nucleotide variant	NM_020378.4(NAT14):c.523G>C (p.Gly175Arg)	not specified [RCV004175407]	uncertain significance	19	55486858	55486858	Human		name
156078121	CV2331937	single nucleotide variant	NM_020378.4(NAT14):c.433G>T (p.Ala145Ser)	not specified [RCV004186588]	uncertain significance	19	55486768	55486768	Human		name
155969070	CV2339381	single nucleotide variant	NM_020378.4(NAT14):c.415G>A (p.Val139Met)	not specified [RCV004191604]	uncertain significance	19	55486750	55486750	Human		name
156174384	CV2345934	single nucleotide variant	NM_198571.3(NAT16):c.388G>A (p.Glu130Lys)	not specified [RCV004198970]	uncertain significance	7	101173445	101173445	Human		name
156113255	CV2349104	single nucleotide variant	NM_020378.4(NAT14):c.379C>T (p.Arg127Cys)	not specified [RCV004205949]	uncertain significance	19	55486714	55486714	Human		name
156259720	CV2366363	single nucleotide variant	NM_024662.3(NAT10):c.863G>A (p.Arg288Gln)	not specified [RCV004212415]	uncertain significance	11	34122541	34122541	Human		name
156339683	CV2367659	single nucleotide variant	NM_198571.3(NAT16):c.571C>G (p.Leu191Val)	not specified [RCV004211578]	uncertain significance	7	101172618	101172618	Human		name
156347273	CV2382870	single nucleotide variant	NM_024662.3(NAT10):c.923A>G (p.Asn308Ser)	not specified [RCV004217471]	uncertain significance	11	34123770	34123770	Human		name
156141334	CV2383683	single nucleotide variant	NM_198571.3(NAT16):c.710T>G (p.Leu237Arg)	not specified [RCV004231573]	uncertain significance	7	101172479	101172479	Human		name
156062857	CV2392163	single nucleotide variant	NM_020378.4(NAT14):c.407G>A (p.Arg136His)	not specified [RCV004238055]	uncertain significance	19	55486742	55486742	Human		name
329368482	CV2428035	single nucleotide variant	NM_198571.3(NAT16):c.705C>G (p.Asp235Glu)	not specified [RCV004254413]	likely benign	7	101172484	101172484	Human		name
329391917	CV2445137	single nucleotide variant	NM_020378.4(NAT14):c.490C>T (p.Arg164Trp)	not specified [RCV004263780]	uncertain significance	19	55486825	55486825	Human		name
401736882	CV2679175	single nucleotide variant	NM_198571.3(NAT16):c.442A>G (p.Lys148Glu)	not specified [RCV004285736]	uncertain significance	7	101173391	101173391	Human		name
401782082	CV2686521	single nucleotide variant	NM_198571.3(NAT16):c.367G>C (p.Gly123Arg)	not specified [RCV004299960]	uncertain significance	7	101173466	101173466	Human		name
401773585	CV2695293	single nucleotide variant	NM_024662.3(NAT10):c.720G>C (p.Glu240Asp)	not specified [RCV004303418]	uncertain significance	11	34118443	34118443	Human		name
401735434	CV2702774	single nucleotide variant	NM_198571.3(NAT16):c.802G>T (p.Val268Leu)	not specified [RCV004319341]	uncertain significance	7	101172387	101172387	Human		name
401773540	CV2709363	single nucleotide variant	NM_198571.3(NAT16):c.773T>A (p.Leu258Gln)	not specified [RCV004316504]	uncertain significance	7	101172416	101172416	Human		name
401775282	CV2710505	single nucleotide variant	NM_020378.4(NAT14):c.545G>A (p.Gly182Asp)	not specified [RCV004319435]	uncertain significance	19	55486880	55486880	Human		name
401763011	CV2720161	single nucleotide variant	NM_198571.3(NAT16):c.445A>G (p.Arg149Gly)	not specified [RCV004323716]	uncertain significance	7	101173388	101173388	Human		name
401892838	CV2758106	single nucleotide variant	NM_198571.3(NAT16):c.346G>A (p.Gly116Arg)	not specified [RCV004341487]	uncertain significance	7	101173487	101173487	Human		name
401860657	CV2758560	single nucleotide variant	NM_198571.3(NAT16):c.353C>A (p.Thr118Lys)	not specified [RCV004337648]	uncertain significance	7	101173480	101173480	Human		name
401884872	CV2766302	single nucleotide variant	NM_198571.3(NAT16):c.377T>C (p.Val126Ala)	not specified [RCV004342558]	uncertain significance	7	101173456	101173456	Human		name
401879482	CV2773120	single nucleotide variant	NM_024662.3(NAT10):c.692C>G (p.Ser231Cys)	not specified [RCV004351545]	uncertain significance	11	34118415	34118415	Human		name
401887819	CV2781694	single nucleotide variant	NM_020378.4(NAT14):c.557A>G (p.Gln186Arg)	not specified [RCV004354888]	uncertain significance	19	55486892	55486892	Human		name
401892432	CV2781943	single nucleotide variant	NM_020378.4(NAT14):c.371G>A (p.Arg124Gln)	not specified [RCV004357179]	uncertain significance	19	55486706	55486706	Human		name
401871916	CV2783634	single nucleotide variant	NM_024662.3(NAT10):c.652G>A (p.Ala218Thr)	not specified [RCV004365948]	uncertain significance	11	34118274	34118274	Human		name
401880815	CV2787645	single nucleotide variant	NM_024662.3(NAT10):c.336G>T (p.Lys112Asn)	not specified [RCV004356574]	uncertain significance	11	34112187	34112187	Human		name
405781552	CV3325090	single nucleotide variant	NM_024662.3(NAT10):c.643A>G (p.Thr215Ala)	not specified [RCV004472047]	uncertain significance	11	34118265	34118265	Human		name
405781645	CV3325105	single nucleotide variant	NM_024662.3(NAT10):c.695A>T (p.Asp232Val)	not specified [RCV004472062]	uncertain significance	11	34118418	34118418	Human		name
405781956	CV3342437	single nucleotide variant	NM_020378.4(NAT14):c.485G>A (p.Arg162Gln)	not specified [RCV004472113]	uncertain significance	19	55486820	55486820	Human		name
405782372	CV3342509	single nucleotide variant	NM_198571.3(NAT16):c.607C>G (p.Arg203Gly)	not specified [RCV004472185]	uncertain significance	7	101172582	101172582	Human		name
405782496	CV3342532	single nucleotide variant	NM_198571.3(NAT16):c.800G>T (p.Arg267Leu)	not specified [RCV004472208]	uncertain significance	7	101172389	101172389	Human		name
405782555	CV3342542	single nucleotide variant	NM_198571.3(NAT16):c.857T>C (p.Ile286Thr)	not specified [RCV004472218]	uncertain significance	7	101172332	101172332	Human		name
407487876	CV3447965	single nucleotide variant	NM_024662.3(NAT10):c.485C>T (p.Thr162Ile)	not specified [RCV004641187]	uncertain significance	11	34113828	34113828	Human		name
407487902	CV3447972	single nucleotide variant	NM_024662.3(NAT10):c.466T>G (p.Ser156Ala)	not specified [RCV004641193]	uncertain significance	11	34113809	34113809	Human		name
407487905	CV3447974	single nucleotide variant	NM_024662.3(NAT10):c.611T>A (p.Leu204His)	not specified [RCV004641194]	uncertain significance	11	34118233	34118233	Human		name
407487908	CV3447975	single nucleotide variant	NM_020378.4(NAT14):c.482C>A (p.Pro161His)	not specified [RCV004641195]	uncertain significance	19	55486817	55486817	Human		name
407487911	CV3447976	single nucleotide variant	NM_020378.4(NAT14):c.455G>C (p.Arg152Pro)	not specified [RCV004641196]	uncertain significance	19	55486790	55486790	Human		name
407487914	CV3447977	single nucleotide variant	NM_020378.4(NAT14):c.523G>A (p.Gly175Arg)	not specified [RCV004641197]	uncertain significance	19	55486858	55486858	Human		name
407520803	CV3458074	single nucleotide variant	NM_020378.4(NAT14):c.569G>C (p.Gly190Ala)	not specified [RCV004652309]	uncertain significance	19	55486904	55486904	Human		name
407520805	CV3458075	single nucleotide variant	NM_198571.3(NAT16):c.666C>G (p.Asp222Glu)	not specified [RCV004652310]	uncertain significance	7	101172523	101172523	Human		name
407520807	CV3458076	single nucleotide variant	NM_198571.3(NAT16):c.486C>G (p.Asp162Glu)	not specified [RCV004652311]	uncertain significance	7	101173347	101173347	Human		name
597655443	CV3565235	single nucleotide variant	NM_024662.3(NAT10):c.902C>T (p.Ala301Val)	not specified [RCV004834136]	uncertain significance	11	34122580	34122580	Human		name
597655182	CV3565236	single nucleotide variant	NM_024662.3(NAT10):c.595G>C (p.Val199Leu)	not specified [RCV004834137]	uncertain significance	11	34118217	34118217	Human		name
597654879	CV3565247	single nucleotide variant	NM_020378.4(NAT14):c.394C>T (p.Arg132Cys)	not specified [RCV004834148]	uncertain significance	19	55486729	55486729	Human		name
597654887	CV3565248	single nucleotide variant	NM_020378.4(NAT14):c.455G>A (p.Arg152Gln)	not specified [RCV004834149]	uncertain significance	19	55486790	55486790	Human		name
597654906	CV3565250	single nucleotide variant	NM_020378.4(NAT14):c.388G>T (p.Val130Phe)	not specified [RCV004834151]	uncertain significance	19	55486723	55486723	Human		name
597654933	CV3565253	single nucleotide variant	NM_198571.3(NAT16):c.491A>G (p.Gln164Arg)	not specified [RCV004834154]	uncertain significance	7	101173342	101173342	Human		name
597654941	CV3565254	single nucleotide variant	NM_198571.3(NAT16):c.602C>T (p.Ala201Val)	not specified [RCV004834155]	uncertain significance	7	101172587	101172587	Human		name
597654947	CV3565255	single nucleotide variant	NM_198571.3(NAT16):c.749G>A (p.Arg250Gln)	not specified [RCV004834156]	uncertain significance	7	101172440	101172440	Human		name
597654965	CV3565257	single nucleotide variant	NM_198571.3(NAT16):c.580G>C (p.Gly194Arg)	not specified [RCV004834158]	likely benign	7	101172609	101172609	Human		name
597654974	CV3565258	single nucleotide variant	NM_198571.3(NAT16):c.325T>A (p.Ser109Thr)	not specified [RCV004834159]	uncertain significance	7	101173508	101173508	Human		name
598215358	CV3983350	single nucleotide variant	NM_024662.3(NAT10):c.802A>G (p.Ile268Val)	not specified [RCV005378737]	uncertain significance	11	34122480	34122480	Human		name
598159361	CV3983353	single nucleotide variant	NM_024662.3(NAT10):c.788C>T (p.Ala263Val)	not specified [RCV005390142]	uncertain significance	11	34122466	34122466	Human		name
598252258	CV3983360	single nucleotide variant	NM_020378.4(NAT14):c.341C>T (p.Ala114Val)	not specified [RCV005385132]	uncertain significance	19	55486676	55486676	Human		name
598215407	CV3983365	single nucleotide variant	NM_198571.3(NAT16):c.473G>A (p.Arg158Gln)	not specified [RCV005378747]	uncertain significance	7	101173360	101173360	Human		name
598252270	CV3983371	single nucleotide variant	NM_198571.3(NAT16):c.988A>C (p.Met330Leu)	not specified [RCV005385134]	uncertain significance	7	101172201	101172201	Human		name
15193446	CV724408	single nucleotide variant	NM_024662.3(NAT10):c.671C>T (p.Pro224Leu)	not provided [RCV000888949]	benign	11	34118293	34118293	Human		name
8632249	CV87457	single nucleotide variant	NM_198571.2(NAT16):c.718G>A (p.Gly240Arg)	Malignant melanoma [RCV000067548]	not provided	7	101172471	101172471	Human		name
150520832	CV1289928	single nucleotide variant	NM_024662.3(NAT10):c.1349C>T (p.Thr450Met)	not provided [RCV001730304]\|not specified [RCV004040020]	likely benign\|uncertain significance	11	34130917	34130917	Human		name
156066822	CV2225604	single nucleotide variant	NM_024662.3(NAT10):c.1160T>C (p.Ile387Thr)	not specified [RCV004100977]	uncertain significance	11	34127515	34127515	Human		name
156068677	CV2237067	single nucleotide variant	NM_024662.3(NAT10):c.1485A>G (p.Ile495Met)	not specified [RCV004114829]	uncertain significance	11	34131496	34131496	Human		name
156141324	CV2247255	single nucleotide variant	NM_024662.3(NAT10):c.2252C>T (p.Thr751Met)	not specified [RCV004114764]	uncertain significance	11	34139231	34139231	Human		name
156219446	CV2254056	single nucleotide variant	NM_024662.3(NAT10):c.2129G>C (p.Gly710Ala)	not specified [RCV004129505]	uncertain significance	11	34136742	34136742	Human		name
156119009	CV2279200	single nucleotide variant	NM_024662.3(NAT10):c.2207C>T (p.Thr736Ile)	not specified [RCV004139432]	uncertain significance	11	34137022	34137022	Human		name
155940602	CV2294107	single nucleotide variant	NM_024662.3(NAT10):c.2284G>A (p.Gly762Ser)	not specified [RCV004149477]	uncertain significance	11	34139263	34139263	Human		name
156197933	CV2306836	single nucleotide variant	NM_198571.3(NAT16):c.1097A>G (p.Glu366Gly)	not specified [RCV004159403]	uncertain significance	7	101172092	101172092	Human		name
156065068	CV2348717	single nucleotide variant	NM_024662.3(NAT10):c.2163G>T (p.Lys721Asn)	not specified [RCV004201128]	uncertain significance	11	34136978	34136978	Human		name
156066062	CV2348960	single nucleotide variant	NM_024662.3(NAT10):c.2470C>G (p.Arg824Gly)	not specified [RCV004203393]	uncertain significance	11	34140450	34140450	Human		name
156340109	CV2351714	single nucleotide variant	NM_024662.3(NAT10):c.2609T>C (p.Ile870Thr)	not specified [RCV004195419]	uncertain significance	11	34141105	34141105	Human		name
156011830	CV2358792	single nucleotide variant	NM_024662.3(NAT10):c.1598A>G (p.Tyr533Cys)	not specified [RCV004212144]	uncertain significance	11	34132202	34132202	Human		name
156098423	CV2385064	single nucleotide variant	NM_024662.3(NAT10):c.1414G>A (p.Ala472Thr)	not specified [RCV004228329]	uncertain significance	11	34131425	34131425	Human		name
156043171	CV2387940	single nucleotide variant	NM_024662.3(NAT10):c.1582C>T (p.Arg528Trp)	not specified [RCV004236483]	uncertain significance	11	34132186	34132186	Human		name
329382611	CV2449223	single nucleotide variant	NM_024662.3(NAT10):c.2701A>G (p.Lys901Glu)	not specified [RCV004257363]	uncertain significance	11	34141197	34141197	Human		name
329402944	CV2462051	single nucleotide variant	NM_024662.3(NAT10):c.2471G>A (p.Arg824Gln)	not specified [RCV004266092]	uncertain significance	11	34140451	34140451	Human		name
329392672	CV2471480	single nucleotide variant	NM_024662.3(NAT10):c.1965G>T (p.Arg655Ser)	not specified [RCV004280476]	uncertain significance	11	34135228	34135228	Human		name
401745255	CV2698500	single nucleotide variant	NM_024662.3(NAT10):c.2848A>C (p.Lys950Gln)	not specified [RCV004298999]	uncertain significance	11	34142311	34142311	Human		name
401735159	CV2699183	single nucleotide variant	NM_024662.3(NAT10):c.2959A>C (p.Ser987Arg)	not specified [RCV004303681]	uncertain significance	11	34143518	34143518	Human		name
401771186	CV2726392	single nucleotide variant	NM_024662.3(NAT10):c.2132T>C (p.Val711Ala)	not specified [RCV004328607]	uncertain significance	11	34136745	34136745	Human		name
401872122	CV2769615	single nucleotide variant	NM_024662.3(NAT10):c.2972A>G (p.Asp991Gly)	not specified [RCV004351258]	uncertain significance	11	34146086	34146086	Human		name
405780962	CV3324990	single nucleotide variant	NM_024662.3(NAT10):c.1414G>T (p.Ala472Ser)	not specified [RCV004471947]	uncertain significance	11	34131425	34131425	Human		name
405781042	CV3325004	single nucleotide variant	NM_024662.3(NAT10):c.1507G>A (p.Glu503Lys)	not specified [RCV004471961]	uncertain significance	11	34131518	34131518	Human		name
405781090	CV3325013	single nucleotide variant	NM_024662.3(NAT10):c.1588A>G (p.Met530Val)	not specified [RCV004471970]	uncertain significance	11	34132192	34132192	Human		name
405781137	CV3325022	single nucleotide variant	NM_024662.3(NAT10):c.1759C>T (p.Arg587Cys)	not specified [RCV004471979]	uncertain significance	11	34134343	34134343	Human		name
405781162	CV3325026	single nucleotide variant	NM_024662.3(NAT10):c.1879G>A (p.Val627Ile)	not specified [RCV004471983]	uncertain significance	11	34134554	34134554	Human		name
405781267	CV3325044	single nucleotide variant	NM_024662.3(NAT10):c.2216A>G (p.Asp739Gly)	not specified [RCV004472001]	uncertain significance	11	34139195	34139195	Human		name
405781326	CV3325054	single nucleotide variant	NM_024662.3(NAT10):c.2516T>C (p.Met839Thr)	not specified [RCV004472011]	uncertain significance	11	34140496	34140496	Human		name
405781394	CV3325065	single nucleotide variant	NM_024662.3(NAT10):c.2852A>G (p.Glu951Gly)	not specified [RCV004472022]	uncertain significance	11	34142315	34142315	Human		name
405782061	CV3342455	single nucleotide variant	NM_198571.3(NAT16):c.1004T>G (p.Leu335Arg)	not specified [RCV004472131]	uncertain significance	7	101172185	101172185	Human		name
407520791	CV3447964	single nucleotide variant	NM_024662.3(NAT10):c.2690G>A (p.Arg897Gln)	not specified [RCV004652305]	uncertain significance	11	34141186	34141186	Human		name
407520794	CV3447966	single nucleotide variant	NM_024662.3(NAT10):c.2878C>T (p.Leu960Phe)	not specified [RCV004652306]	uncertain significance	11	34142341	34142341	Human		name
407487881	CV3447967	single nucleotide variant	NM_024662.3(NAT10):c.2762C>T (p.Ala921Val)	not specified [RCV004641188]	likely benign	11	34141768	34141768	Human		name
407487885	CV3447968	single nucleotide variant	NM_024662.3(NAT10):c.1843G>A (p.Asp615Asn)	not specified [RCV004641189]	uncertain significance	11	34134518	34134518	Human		name
407487889	CV3447969	single nucleotide variant	NM_024662.3(NAT10):c.2063G>A (p.Arg688Gln)	not specified [RCV004641190]	uncertain significance	11	34136676	34136676	Human		name
407487894	CV3447970	single nucleotide variant	NM_024662.3(NAT10):c.1924A>C (p.Ser642Arg)	not specified [RCV004641191]	uncertain significance	11	34135187	34135187	Human		name
407487898	CV3447971	single nucleotide variant	NM_024662.3(NAT10):c.1988T>C (p.Val663Ala)	not specified [RCV004641192]	uncertain significance	11	34135251	34135251	Human		name
597654957	CV3565237	single nucleotide variant	NM_024662.3(NAT10):c.2897G>A (p.Arg966His)	not specified [RCV004834138]	uncertain significance	11	34143456	34143456	Human		name
597654806	CV3565238	single nucleotide variant	NM_024662.3(NAT10):c.2174G>A (p.Arg725Gln)	not specified [RCV004834139]	uncertain significance	11	34136989	34136989	Human		name
597654812	CV3565239	single nucleotide variant	NM_024662.3(NAT10):c.1481G>A (p.Arg494Gln)	not specified [RCV004834140]	uncertain significance	11	34131492	34131492	Human		name
597654820	CV3565240	single nucleotide variant	NM_024662.3(NAT10):c.1447G>A (p.Asp483Asn)	not specified [RCV004834141]	uncertain significance	11	34131458	34131458	Human		name
597654829	CV3565241	single nucleotide variant	NM_024662.3(NAT10):c.2470C>T (p.Arg824Trp)	not specified [RCV004834142]	uncertain significance	11	34140450	34140450	Human		name
597654837	CV3565242	single nucleotide variant	NM_024662.3(NAT10):c.1279C>G (p.Leu427Val)	not specified [RCV004834143]	uncertain significance	11	34130847	34130847	Human		name
597654852	CV3565244	single nucleotide variant	NM_024662.3(NAT10):c.1591G>A (p.Ala531Thr)	not specified [RCV004834145]	uncertain significance	11	34132195	34132195	Human		name
597654859	CV3565245	single nucleotide variant	NM_024662.3(NAT10):c.2795C>T (p.Thr932Ile)	not specified [RCV004834146]	uncertain significance	11	34141801	34141801	Human		name
597654870	CV3565246	single nucleotide variant	NM_024662.3(NAT10):c.2858G>T (p.Gly953Val)	not specified [RCV004834147]	uncertain significance	11	34142321	34142321	Human		name
598159358	CV3983351	single nucleotide variant	NM_024662.3(NAT10):c.2095A>G (p.Asn699Asp)	not specified [RCV005390141]	uncertain significance	11	34136708	34136708	Human		name
598159365	CV3983355	single nucleotide variant	NM_024662.3(NAT10):c.2317C>T (p.Arg773Trp)	not specified [RCV005390143]	uncertain significance	11	34139393	34139393	Human		name
598252253	CV3983356	single nucleotide variant	NM_024662.3(NAT10):c.2222C>T (p.Thr741Ile)	not specified [RCV005385131]	uncertain significance	11	34139201	34139201	Human		name
598215373	CV3983357	single nucleotide variant	NM_024662.3(NAT10):c.1112T>C (p.Ile371Thr)	not specified [RCV005378740]	uncertain significance	11	34127467	34127467	Human		name
598215382	CV3983359	single nucleotide variant	NM_024662.3(NAT10):c.1355C>T (p.Ala452Val)	not specified [RCV005378742]	uncertain significance	11	34130923	34130923	Human		name
598215418	CV3983368	single nucleotide variant	NM_198571.3(NAT16):c.1045G>C (p.Val349Leu)	not specified [RCV005378749]	uncertain significance	7	101172144	101172144	Human		name
598215434	CV3983372	single nucleotide variant	NM_198571.3(NAT16):c.1087T>C (p.Tyr363His)	not specified [RCV005378752]	uncertain significance	7	101172102	101172102	Human		name
15134690	CV712798	single nucleotide variant	NM_024662.3(NAT10):c.2786C>T (p.Thr929Met)	not provided [RCV000965167]	likely benign	11	34141792	34141792	Human		name
15162179	CV712799	single nucleotide variant	NM_024662.3(NAT10):c.2947G>A (p.Ala983Thr)	not provided [RCV000970225]	benign	11	34143506	34143506	Human		name
156179724	CV2298399	single nucleotide variant	NM_024662.3(NAT10):c.3067C>T (p.Arg1023Trp)	not specified [RCV004162075]	uncertain significance	11	34146181	34146181	Human		name

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