Kbtbd11 Variant Search Result - Rat Genome Database

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121 records found for search term Kbtbd11

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156037136	CV2250129	single nucleotide variant	NM_014867.3(KBTBD11):c.88C>G (p.Pro30Ala)	not specified [RCV004116940]	uncertain significance	8	2001280	2001280	Human		name
156266813	CV2329631	single nucleotide variant	NM_014867.3(KBTBD11):c.29T>C (p.Leu10Pro)	not specified [RCV004180747]	uncertain significance	8	2001221	2001221	Human		name
597787020	CV3690957	single nucleotide variant	NM_014867.3(KBTBD11):c.35C>G (p.Pro12Arg)	not specified [RCV004932374]	uncertain significance	8	2001227	2001227	Human		name
597787050	CV3690964	single nucleotide variant	NM_014867.3(KBTBD11):c.61G>A (p.Glu21Lys)	not specified [RCV004932381]	uncertain significance	8	2001253	2001253	Human		name
597787068	CV3690968	single nucleotide variant	NM_014867.3(KBTBD11):c.28C>T (p.Leu10Phe)	not specified [RCV004932385]	uncertain significance	8	2001220	2001220	Human		name
156274855	CV2287534	single nucleotide variant	NM_014867.3(KBTBD11):c.119C>T (p.Ser40Phe)	not specified [RCV004140988]	uncertain significance	8	2001311	2001311	Human		name
155921979	CV2340544	single nucleotide variant	NM_014867.3(KBTBD11):c.212C>G (p.Pro71Arg)	not specified [RCV004197260]	uncertain significance	8	2001404	2001404	Human		name
156233217	CV2346179	single nucleotide variant	NM_014867.3(KBTBD11):c.278C>T (p.Ser93Phe)	not specified [RCV004201636]	uncertain significance	8	2001470	2001470	Human		name
156337312	CV2360936	single nucleotide variant	NM_014867.3(KBTBD11):c.239C>T (p.Ala80Val)	not specified [RCV004215749]	likely benign	8	2001431	2001431	Human		name
156168888	CV2399194	single nucleotide variant	NM_014867.3(KBTBD11):c.194C>T (p.Pro65Leu)	not specified [RCV004246623]	uncertain significance	8	2001386	2001386	Human		name
401724689	CV2714931	single nucleotide variant	NM_014867.3(KBTBD11):c.100C>A (p.Pro34Thr)	not specified [RCV004322261]	uncertain significance	8	2001292	2001292	Human		name
405802297	CV3272139	single nucleotide variant	NM_014867.3(KBTBD11):c.223G>A (p.Glu75Lys)	not specified [RCV004403838]	uncertain significance	8	2001415	2001415	Human		name
405802299	CV3272140	single nucleotide variant	NM_014867.3(KBTBD11):c.231G>C (p.Gln77His)	not specified [RCV004403839]	uncertain significance	8	2001423	2001423	Human		name
407511707	CV3448368	single nucleotide variant	NM_014867.3(KBTBD11):c.131G>A (p.Ser44Asn)	not specified [RCV004626552]	uncertain significance	8	2001323	2001323	Human		name
597787001	CV3690953	single nucleotide variant	NM_014867.3(KBTBD11):c.289C>T (p.Arg97Cys)	not specified [RCV004932370]	uncertain significance	8	2001481	2001481	Human		name
597787087	CV3690972	single nucleotide variant	NM_014867.3(KBTBD11):c.185C>G (p.Ala62Gly)	not specified [RCV004932389]	uncertain significance	8	2001377	2001377	Human		name
597787091	CV3690973	single nucleotide variant	NM_014867.3(KBTBD11):c.267G>C (p.Glu89Asp)	not specified [RCV004932390]	uncertain significance	8	2001459	2001459	Human		name
598212633	CV3980058	single nucleotide variant	NM_014867.3(KBTBD11):c.224A>T (p.Glu75Val)	not specified [RCV005358851]	uncertain significance	8	2001416	2001416	Human		name
598212639	CV3980067	single nucleotide variant	NM_014867.3(KBTBD11):c.169G>A (p.Ala57Thr)	not specified [RCV005358852]	uncertain significance	8	2001361	2001361	Human		name
598234474	CV3980071	single nucleotide variant	NM_014867.3(KBTBD11):c.230A>G (p.Gln77Arg)	not specified [RCV005363514]	uncertain significance	8	2001422	2001422	Human		name
598234483	CV3980072	single nucleotide variant	NM_014867.3(KBTBD11):c.278C>A (p.Ser93Tyr)	not specified [RCV005363515]	uncertain significance	8	2001470	2001470	Human		name
155962668	CV2197620	single nucleotide variant	NM_014867.3(KBTBD11):c.908C>T (p.Pro303Leu)	not specified [RCV004074837]	uncertain significance	8	2002100	2002100	Human		name
156144274	CV2208723	single nucleotide variant	NM_014867.3(KBTBD11):c.959A>C (p.Asp320Ala)	not specified [RCV004084913]	uncertain significance	8	2002151	2002151	Human		name
155946006	CV2238061	single nucleotide variant	NM_014867.3(KBTBD11):c.785A>G (p.His262Arg)	not specified [RCV004111087]	uncertain significance	8	2001977	2001977	Human		name
156031965	CV2239282	single nucleotide variant	NM_014867.3(KBTBD11):c.440C>G (p.Ser147Trp)	not specified [RCV004112244]	uncertain significance	8	2001632	2001632	Human		name
156075008	CV2247959	single nucleotide variant	NM_014867.3(KBTBD11):c.662A>C (p.Gln221Pro)	not specified [RCV004121391]	uncertain significance	8	2001854	2001854	Human		name
155919096	CV2254804	single nucleotide variant	NM_014867.3(KBTBD11):c.671C>T (p.Thr224Ile)	not specified [RCV004115271]	uncertain significance	8	2001863	2001863	Human		name
156032374	CV2259591	single nucleotide variant	NM_014867.3(KBTBD11):c.715G>A (p.Val239Ile)	not specified [RCV004116636]	uncertain significance	8	2001907	2001907	Human		name
156255755	CV2264753	single nucleotide variant	NM_014867.3(KBTBD11):c.821G>T (p.Gly274Val)	not specified [RCV004132732]	uncertain significance	8	2002013	2002013	Human		name
156167736	CV2279865	single nucleotide variant	NM_014867.3(KBTBD11):c.353C>T (p.Ala118Val)	not specified [RCV004144459]	uncertain significance	8	2001545	2001545	Human		name
155981908	CV2337103	single nucleotide variant	NM_014867.3(KBTBD11):c.388C>T (p.Pro130Ser)	not specified [RCV004192866]	uncertain significance	8	2001580	2001580	Human		name
156190995	CV2339706	single nucleotide variant	NM_014867.3(KBTBD11):c.583C>T (p.Arg195Cys)	not specified [RCV004196408]	uncertain significance	8	2001775	2001775	Human		name
156078476	CV2341191	single nucleotide variant	NM_014867.3(KBTBD11):c.796G>A (p.Val266Met)	not specified [RCV004186610]	uncertain significance	8	2001988	2001988	Human		name
155927759	CV2349746	single nucleotide variant	NM_014867.3(KBTBD11):c.619G>T (p.Val207Leu)	not specified [RCV004204160]	uncertain significance	8	2001811	2001811	Human		name
156190925	CV2356801	single nucleotide variant	NM_014867.3(KBTBD11):c.389C>T (p.Pro130Leu)	not specified [RCV004202142]	uncertain significance	8	2001581	2001581	Human		name
156188877	CV2375441	single nucleotide variant	NM_014867.3(KBTBD11):c.680T>C (p.Val227Ala)	not specified [RCV004225959]	uncertain significance	8	2001872	2001872	Human		name
155970293	CV2392186	single nucleotide variant	NM_014867.3(KBTBD11):c.724G>A (p.Ala242Thr)	not specified [RCV004242533]	uncertain significance	8	2001916	2001916	Human		name
329367424	CV2456846	single nucleotide variant	NM_014867.3(KBTBD11):c.443G>C (p.Gly148Ala)	not specified [RCV004270809]	uncertain significance	8	2001635	2001635	Human		name
329392094	CV2470370	single nucleotide variant	NM_014867.3(KBTBD11):c.340C>T (p.Leu114Phe)	not specified [RCV004279752]	uncertain significance	8	2001532	2001532	Human		name
401749377	CV2694632	single nucleotide variant	NM_014867.3(KBTBD11):c.901C>G (p.Leu301Val)	not specified [RCV004298744]	uncertain significance	8	2002093	2002093	Human		name
401764563	CV2705094	single nucleotide variant	NM_014867.3(KBTBD11):c.979G>A (p.Val327Ile)	not specified [RCV004310001]	uncertain significance	8	2002171	2002171	Human		name
401863779	CV2773312	single nucleotide variant	NM_014867.3(KBTBD11):c.781G>A (p.Asp261Asn)	not specified [RCV004353977]	uncertain significance	8	2001973	2001973	Human		name
401882730	CV2778476	single nucleotide variant	NM_014867.3(KBTBD11):c.682G>T (p.Gly228Trp)	not specified [RCV004344140]	uncertain significance	8	2001874	2001874	Human		name
401872510	CV2779699	single nucleotide variant	NM_014867.3(KBTBD11):c.439T>C (p.Ser147Pro)	not specified [RCV004351388]	uncertain significance	8	2001631	2001631	Human		name
405802300	CV3272141	single nucleotide variant	NM_014867.3(KBTBD11):c.406G>A (p.Val136Met)	not specified [RCV004403840]	uncertain significance	8	2001598	2001598	Human		name
405802302	CV3272142	single nucleotide variant	NM_014867.3(KBTBD11):c.580G>A (p.Gly194Arg)	not specified [RCV004403841]	uncertain significance	8	2001772	2001772	Human		name
405802304	CV3272143	single nucleotide variant	NM_014867.3(KBTBD11):c.714G>C (p.Glu238Asp)	not specified [RCV004403842]	uncertain significance	8	2001906	2001906	Human		name
405802306	CV3272144	single nucleotide variant	NM_014867.3(KBTBD11):c.751C>G (p.Leu251Val)	not specified [RCV004403843]	uncertain significance	8	2001943	2001943	Human		name
405802308	CV3272145	single nucleotide variant	NM_014867.3(KBTBD11):c.770G>A (p.Cys257Tyr)	not specified [RCV004403844]	uncertain significance	8	2001962	2001962	Human		name
405802310	CV3272146	single nucleotide variant	NM_014867.3(KBTBD11):c.950G>C (p.Gly317Ala)	not specified [RCV004403845]	uncertain significance	8	2002142	2002142	Human		name
405802312	CV3272147	single nucleotide variant	NM_014867.3(KBTBD11):c.983A>C (p.Tyr328Ser)	not specified [RCV004403846]	uncertain significance	8	2002175	2002175	Human		name
405802314	CV3272148	single nucleotide variant	NM_014867.3(KBTBD11):c.990C>A (p.Phe330Leu)	not specified [RCV004403847]	uncertain significance	8	2002182	2002182	Human		name
407467711	CV3448364	single nucleotide variant	NM_014867.3(KBTBD11):c.683G>C (p.Gly228Ala)	not specified [RCV004635979]	uncertain significance	8	2001875	2001875	Human		name
407467713	CV3448366	single nucleotide variant	NM_014867.3(KBTBD11):c.689A>C (p.Gln230Pro)	not specified [RCV004635980]	uncertain significance	8	2001881	2001881	Human		name
407467719	CV3448370	single nucleotide variant	NM_014867.3(KBTBD11):c.599G>A (p.Arg200Gln)	not specified [RCV004635982]	uncertain significance	8	2001791	2001791	Human		name
597786981	CV3690948	single nucleotide variant	NM_014867.3(KBTBD11):c.733C>T (p.Arg245Trp)	not specified [RCV004932365]	uncertain significance	8	2001925	2001925	Human		name
597786989	CV3690950	single nucleotide variant	NM_014867.3(KBTBD11):c.859C>G (p.Arg287Gly)	not specified [RCV004932367]	uncertain significance	8	2002051	2002051	Human		name
597787012	CV3690955	single nucleotide variant	NM_014867.3(KBTBD11):c.704A>C (p.Asn235Thr)	not specified [RCV004932372]	uncertain significance	8	2001896	2001896	Human		name
597787046	CV3690963	single nucleotide variant	NM_014867.3(KBTBD11):c.922G>A (p.Ala308Thr)	not specified [RCV004932380]	uncertain significance	8	2002114	2002114	Human		name
597787063	CV3690967	single nucleotide variant	NM_014867.3(KBTBD11):c.628G>T (p.Gly210Cys)	not specified [RCV004932384]	uncertain significance	8	2001820	2001820	Human		name
597787081	CV3690971	single nucleotide variant	NM_014867.3(KBTBD11):c.704A>G (p.Asn235Ser)	not specified [RCV004932388]	uncertain significance	8	2001896	2001896	Human		name
598234435	CV3980057	single nucleotide variant	NM_014867.3(KBTBD11):c.346G>A (p.Asp116Asn)	not specified [RCV005363509]	uncertain significance	8	2001538	2001538	Human		name
598234451	CV3980061	single nucleotide variant	NM_014867.3(KBTBD11):c.331C>T (p.Arg111Cys)	not specified [RCV005363511]	uncertain significance	8	2001523	2001523	Human		name
598259239	CV3980062	single nucleotide variant	NM_014867.3(KBTBD11):c.838G>A (p.Glu280Lys)	not specified [RCV005347377]	uncertain significance	8	2002030	2002030	Human		name
598259242	CV3980063	single nucleotide variant	NM_014867.3(KBTBD11):c.391C>G (p.Pro131Ala)	not specified [RCV005347378]	uncertain significance	8	2001583	2001583	Human		name
598259247	CV3980064	single nucleotide variant	NM_014867.3(KBTBD11):c.880G>A (p.Ala294Thr)	not specified [RCV005347379]	uncertain significance	8	2002072	2002072	Human		name
598259253	CV3980066	single nucleotide variant	NM_014867.3(KBTBD11):c.382C>T (p.Pro128Ser)	not specified [RCV005347380]	uncertain significance	8	2001574	2001574	Human		name
598259262	CV3980070	single nucleotide variant	NM_014867.3(KBTBD11):c.893C>T (p.Ala298Val)	not specified [RCV005347382]	uncertain significance	8	2002085	2002085	Human		name
598259266	CV3980073	single nucleotide variant	NM_014867.3(KBTBD11):c.386T>A (p.Val129Glu)	not specified [RCV005347383]	uncertain significance	8	2001578	2001578	Human		name
156382825	CV2223655	single nucleotide variant	NM_014867.3(KBTBD11):c.1100T>G (p.Val367Gly)	not specified [RCV004093778]	uncertain significance	8	2002292	2002292	Human		name
156343524	CV2232783	single nucleotide variant	NM_014867.3(KBTBD11):c.1280G>T (p.Arg427Leu)	not specified [RCV004101420]	uncertain significance	8	2002472	2002472	Human		name
155922509	CV2240702	single nucleotide variant	NM_014867.3(KBTBD11):c.1577G>C (p.Arg526Pro)	not specified [RCV004119328]	uncertain significance	8	2002769	2002769	Human		name
156127938	CV2244774	single nucleotide variant	NM_014867.3(KBTBD11):c.1088T>G (p.Val363Gly)	not specified [RCV004102758]	uncertain significance	8	2002280	2002280	Human		name
155919497	CV2254882	single nucleotide variant	NM_014867.3(KBTBD11):c.1576C>G (p.Arg526Gly)	not specified [RCV004117128]	uncertain significance	8	2002768	2002768	Human		name
155965472	CV2261800	single nucleotide variant	NM_014867.3(KBTBD11):c.1066G>A (p.Val356Ile)	not specified [RCV004126080]	uncertain significance	8	2002258	2002258	Human		name
156018590	CV2272318	single nucleotide variant	NM_014867.3(KBTBD11):c.1531C>T (p.Arg511Cys)	not specified [RCV004131465]	uncertain significance	8	2002723	2002723	Human		name
156331006	CV2339565	single nucleotide variant	NM_014867.3(KBTBD11):c.1559G>A (p.Ser520Asn)	not specified [RCV004194230]	uncertain significance	8	2002751	2002751	Human		name
156175811	CV2374402	single nucleotide variant	NM_014867.3(KBTBD11):c.1147T>G (p.Phe383Val)	not specified [RCV004231920]	uncertain significance	8	2002339	2002339	Human		name
156008220	CV2390087	single nucleotide variant	NM_014867.3(KBTBD11):c.1004G>T (p.Gly335Val)	not specified [RCV004238689]	uncertain significance	8	2002196	2002196	Human		name
156143908	CV2393623	single nucleotide variant	NM_014867.3(KBTBD11):c.1103C>G (p.Ala368Gly)	not specified [RCV004231435]	uncertain significance	8	2002295	2002295	Human		name
156105625	CV2400383	single nucleotide variant	NM_014867.3(KBTBD11):c.1784G>T (p.Gly595Val)	not specified [RCV004244434]	uncertain significance	8	2002976	2002976	Human		name
329363712	CV2465116	single nucleotide variant	NM_014867.3(KBTBD11):c.1643C>T (p.Thr548Met)	not specified [RCV004286840]	uncertain significance	8	2002835	2002835	Human		name
329380462	CV2466634	single nucleotide variant	NM_014867.3(KBTBD11):c.1448G>A (p.Cys483Tyr)	not specified [RCV004274156]	uncertain significance	8	2002640	2002640	Human		name
401720974	CV2702213	single nucleotide variant	NM_014867.3(KBTBD11):c.1624C>G (p.Arg542Gly)	not specified [RCV004314558]	uncertain significance	8	2002816	2002816	Human		name
401751451	CV2708631	single nucleotide variant	NM_014867.3(KBTBD11):c.1547C>T (p.Ala516Val)	not specified [RCV004307615]	uncertain significance	8	2002739	2002739	Human		name
401771694	CV2711839	single nucleotide variant	NM_014867.3(KBTBD11):c.1765G>A (p.Gly589Ser)	not specified [RCV004309473]	uncertain significance	8	2002957	2002957	Human		name
401751168	CV2712431	single nucleotide variant	NM_014867.3(KBTBD11):c.1234G>C (p.Gly412Arg)	not specified [RCV004313896]	uncertain significance	8	2002426	2002426	Human		name
401870567	CV2758943	single nucleotide variant	NM_014867.3(KBTBD11):c.1114C>A (p.Pro372Thr)	not specified [RCV004342259]	uncertain significance	8	2002306	2002306	Human		name
401885189	CV2771007	single nucleotide variant	NM_014867.3(KBTBD11):c.1022C>T (p.Thr341Met)	not specified [RCV004344023]	uncertain significance	8	2002214	2002214	Human		name
401881882	CV2774645	single nucleotide variant	NM_014867.3(KBTBD11):c.1699C>T (p.Arg567Cys)	not specified [RCV004350110]	uncertain significance	8	2002891	2002891	Human		name
401892213	CV2777328	single nucleotide variant	NM_014867.3(KBTBD11):c.1057G>A (p.Gly353Ser)	not specified [RCV004354341]	uncertain significance	8	2002249	2002249	Human		name
401896647	CV2791637	single nucleotide variant	NM_014867.3(KBTBD11):c.1484T>C (p.Met495Thr)	not specified [RCV004352985]	uncertain significance	8	2002676	2002676	Human		name
405802280	CV3272130	single nucleotide variant	NM_014867.3(KBTBD11):c.1091C>T (p.Ala364Val)	not specified [RCV004403829]	uncertain significance	8	2002283	2002283	Human		name
405802282	CV3272131	single nucleotide variant	NM_014867.3(KBTBD11):c.1178G>A (p.Ser393Asn)	not specified [RCV004403830]	uncertain significance	8	2002370	2002370	Human		name
405802284	CV3272132	single nucleotide variant	NM_014867.3(KBTBD11):c.1260G>C (p.Glu420Asp)	not specified [RCV004403831]	uncertain significance	8	2002452	2002452	Human		name
405802288	CV3272134	single nucleotide variant	NM_014867.3(KBTBD11):c.1307C>T (p.Ala436Val)	not specified [RCV004403833]	uncertain significance	8	2002499	2002499	Human		name
405802289	CV3272135	single nucleotide variant	NM_014867.3(KBTBD11):c.1574C>T (p.Ser525Phe)	not specified [RCV004403834]	likely benign	8	2002766	2002766	Human		name
405802291	CV3272136	single nucleotide variant	NM_014867.3(KBTBD11):c.1693G>T (p.Val565Leu)	not specified [RCV004403835]	uncertain significance	8	2002885	2002885	Human		name
405802293	CV3272137	single nucleotide variant	NM_014867.3(KBTBD11):c.1798G>T (p.Val600Phe)	not specified [RCV004403836]	uncertain significance	8	2002990	2002990	Human		name
405802295	CV3272138	single nucleotide variant	NM_014867.3(KBTBD11):c.1850G>T (p.Arg617Leu)	not specified [RCV004403837]	uncertain significance	8	2003042	2003042	Human		name
407511704	CV3448365	single nucleotide variant	NM_014867.3(KBTBD11):c.1621C>G (p.Leu541Val)	not specified [RCV004626551]	uncertain significance	8	2002813	2002813	Human		name
407467716	CV3448367	single nucleotide variant	NM_014867.3(KBTBD11):c.1369G>T (p.Gly457Cys)	not specified [RCV004635981]	uncertain significance	8	2002561	2002561	Human		name
407511711	CV3448369	single nucleotide variant	NM_014867.3(KBTBD11):c.1676A>T (p.Asp559Val)	not specified [RCV004626553]	uncertain significance	8	2002868	2002868	Human		name
407467722	CV3448371	single nucleotide variant	NM_014867.3(KBTBD11):c.1669G>A (p.Ala557Thr)	not specified [RCV004635983]	uncertain significance	8	2002861	2002861	Human		name
407467725	CV3448372	single nucleotide variant	NM_014867.3(KBTBD11):c.1463G>A (p.Ser488Asn)	not specified [RCV004635984]	uncertain significance	8	2002655	2002655	Human		name
597786993	CV3690951	single nucleotide variant	NM_014867.3(KBTBD11):c.1342G>A (p.Val448Met)	not specified [RCV004932368]	uncertain significance	8	2002534	2002534	Human		name
597786997	CV3690952	single nucleotide variant	NM_014867.3(KBTBD11):c.1480G>A (p.Asp494Asn)	not specified [RCV004932369]	uncertain significance	8	2002672	2002672	Human		name
597787006	CV3690954	single nucleotide variant	NM_014867.3(KBTBD11):c.1823C>T (p.Ala608Val)	not specified [RCV004932371]	likely benign	8	2003015	2003015	Human		name
597787016	CV3690956	single nucleotide variant	NM_014867.3(KBTBD11):c.1004G>C (p.Gly335Ala)	not specified [RCV004932373]	uncertain significance	8	2002196	2002196	Human		name
597787024	CV3690958	single nucleotide variant	NM_014867.3(KBTBD11):c.1312G>A (p.Val438Met)	not specified [RCV004932375]	uncertain significance	8	2002504	2002504	Human		name
597787032	CV3690960	single nucleotide variant	NM_014867.3(KBTBD11):c.1211A>T (p.Gln404Leu)	not specified [RCV004932377]	uncertain significance	8	2002403	2002403	Human		name
597787036	CV3690961	single nucleotide variant	NM_014867.3(KBTBD11):c.1497C>A (p.Asp499Glu)	not specified [RCV004932378]	uncertain significance	8	2002689	2002689	Human		name
597787040	CV3690962	single nucleotide variant	NM_014867.3(KBTBD11):c.1534G>A (p.Gly512Ser)	not specified [RCV004932379]	uncertain significance	8	2002726	2002726	Human		name
597787054	CV3690965	single nucleotide variant	NM_014867.3(KBTBD11):c.1021A>G (p.Thr341Ala)	not specified [RCV004932382]	uncertain significance	8	2002213	2002213	Human		name
597787058	CV3690966	single nucleotide variant	NM_014867.3(KBTBD11):c.1051G>A (p.Gly351Ser)	not specified [RCV004932383]	uncertain significance	8	2002243	2002243	Human		name
597787072	CV3690969	single nucleotide variant	NM_014867.3(KBTBD11):c.1550C>T (p.Ala517Val)	not specified [RCV004932386]	uncertain significance	8	2002742	2002742	Human		name
597787095	CV3690974	single nucleotide variant	NM_014867.3(KBTBD11):c.1264C>G (p.Leu422Val)	not specified [RCV004932391]	uncertain significance	8	2002456	2002456	Human		name
598259234	CV3980059	single nucleotide variant	NM_014867.3(KBTBD11):c.1744G>A (p.Gly582Ser)	not specified [RCV005347376]	uncertain significance	8	2002936	2002936	Human		name
598234443	CV3980060	single nucleotide variant	NM_014867.3(KBTBD11):c.1864G>A (p.Ala622Thr)	not specified [RCV005363510]	uncertain significance	8	2003056	2003056	Human		name
598259257	CV3980068	single nucleotide variant	NM_014867.3(KBTBD11):c.1607C>G (p.Pro536Arg)	not specified [RCV005347381]	uncertain significance	8	2002799	2002799	Human		name
598234464	CV3980069	single nucleotide variant	NM_014867.3(KBTBD11):c.1067T>C (p.Val356Ala)	not specified [RCV005363513]	uncertain significance	8	2002259	2002259	Human		name

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