Dntt Variant Search Result - Rat Genome Database

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124 records found for search term Dntt

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15184323	CV777900	single nucleotide variant	NM_004088.4(DNTT):c.203+7C>G	not provided [RCV000952678]	benign	10	96304707	96304707	Human		name
15198756	CV777903	single nucleotide variant	NM_004088.4(DNTT):c.203+9G>A	not provided [RCV000956852]	benign	10	96304709	96304709	Human		name
401886785	CV2776737	single nucleotide variant	NM_004088.4(DNTT):c.35G>A (p.Arg12Gln)	not specified [RCV004357891]	uncertain significance	10	96304532	96304532	Human		name
598174258	CV3964346	single nucleotide variant	NM_004088.4(DNTT):c.34C>T (p.Arg12Trp)	not specified [RCV005331665]	uncertain significance	10	96304531	96304531	Human		name
15111222	CV712535	single nucleotide variant	NM_004088.4(DNTT):c.732A>G (p.Glu244=)	not provided [RCV000961063]	benign\|likely benign	10	96322710	96322710	Human		name
15159267	CV724134	single nucleotide variant	NM_004088.4(DNTT):c.495C>T (p.Asn165=)	not provided [RCV000881162]	benign	10	96319378	96319378	Human		name
15148023	CV737663	single nucleotide variant	NM_004088.4(DNTT):c.387A>G (p.Arg129=)	not provided [RCV000900637]	likely benign	10	96319270	96319270	Human		name
405749153	CV3241104	single nucleotide variant	NM_004088.4(DNTT):c.142C>A (p.Arg48Ser)	not specified [RCV004381707]	uncertain significance	10	96304639	96304639	Human		name
405749165	CV3241106	single nucleotide variant	NM_004088.4(DNTT):c.186G>T (p.Arg62Ser)	not specified [RCV004381709]	uncertain significance	10	96304683	96304683	Human		name
405749171	CV3241107	single nucleotide variant	NM_004088.4(DNTT):c.239C>T (p.Ser80Leu)	not specified [RCV004381710]	uncertain significance	10	96318387	96318387	Human		name
407505424	CV3437712	single nucleotide variant	NM_004088.4(DNTT):c.266A>C (p.Gln89Pro)	not specified [RCV004624355]	uncertain significance	10	96318414	96318414	Human		name
15198760	CV701494	single nucleotide variant	NM_004088.4(DNTT):c.269C>T (p.Ala90Val)	not provided [RCV000956853]	benign	10	96318417	96318417	Human		name
156242348	CV2210652	single nucleotide variant	NM_004088.4(DNTT):c.447G>T (p.Lys149Asn)	not specified [RCV004083795]	uncertain significance	10	96319330	96319330	Human		name
156332171	CV2220638	single nucleotide variant	NM_004088.4(DNTT):c.884A>G (p.Tyr295Cys)	not specified [RCV004097819]	uncertain significance	10	96327477	96327477	Human		name
156296188	CV2318121	single nucleotide variant	NM_004088.4(DNTT):c.631A>T (p.Thr211Ser)	not specified [RCV004177535]	uncertain significance	10	96320741	96320741	Human		name
156162109	CV2323509	single nucleotide variant	NM_004088.4(DNTT):c.419C>G (p.Pro140Arg)	not specified [RCV004165715]	uncertain significance	10	96319302	96319302	Human		name
156154417	CV2328647	single nucleotide variant	NM_004088.4(DNTT):c.410C>T (p.Pro137Leu)	not specified [RCV004177894]	uncertain significance	10	96319293	96319293	Human		name
156054742	CV2388631	single nucleotide variant	NM_004088.4(DNTT):c.327A>T (p.Glu109Asp)	not specified [RCV004239511]	uncertain significance	10	96318475	96318475	Human		name
405749179	CV3241108	single nucleotide variant	NM_004088.4(DNTT):c.563G>A (p.Cys188Tyr)	not specified [RCV004381711]	likely benign	10	96320673	96320673	Human		name
405749188	CV3241109	single nucleotide variant	NM_004088.4(DNTT):c.718G>T (p.Val240Leu)	not specified [RCV004381712]	uncertain significance	10	96322696	96322696	Human		name
405749193	CV3241110	single nucleotide variant	NM_004088.4(DNTT):c.757A>T (p.Thr253Ser)	not specified [RCV004381713]	uncertain significance	10	96324272	96324272	Human		name
405749197	CV3241111	single nucleotide variant	NM_004088.4(DNTT):c.921A>C (p.Glu307Asp)	not specified [RCV004381714]	uncertain significance	10	96327514	96327514	Human		name
407505421	CV3437711	single nucleotide variant	NM_004088.4(DNTT):c.931G>A (p.Val311Ile)	not specified [RCV004624354]	uncertain significance	10	96327524	96327524	Human		name
597660815	CV3659389	single nucleotide variant	NM_004088.4(DNTT):c.581C>T (p.Ala194Val)	not specified [RCV004911807]	uncertain significance	10	96320691	96320691	Human		name
598174250	CV3964345	single nucleotide variant	NM_004088.4(DNTT):c.971C>T (p.Pro324Leu)	not specified [RCV005331664]	uncertain significance	10	96327564	96327564	Human		name
598174266	CV3964347	single nucleotide variant	NM_004088.4(DNTT):c.797G>T (p.Trp266Leu)	not specified [RCV005331666]	uncertain significance	10	96324312	96324312	Human		name
598174282	CV3964349	single nucleotide variant	NM_004088.4(DNTT):c.802A>T (p.Arg268Trp)	not specified [RCV005331668]	uncertain significance	10	96324317	96324317	Human		name
15181979	CV712536	single nucleotide variant	NM_004088.4(DNTT):c.838G>C (p.Asp280His)	not provided [RCV000974522]	likely benign	10	96324353	96324353	Human		name
156135642	CV2196108	single nucleotide variant	NM_004088.4(DNTT):c.1004G>A (p.Arg335Gln)	not specified [RCV004073472]	uncertain significance	10	96327597	96327597	Human		name
156088099	CV2201962	single nucleotide variant	NM_004088.4(DNTT):c.1526C>T (p.Ala509Val)	not specified [RCV004075891]	uncertain significance	10	96338220	96338220	Human		name
156305911	CV2314774	single nucleotide variant	NM_004088.4(DNTT):c.1232G>A (p.Arg411His)	not specified [RCV004170909]	likely benign	10	96332469	96332469	Human		name
155901498	CV2345816	single nucleotide variant	NM_004088.4(DNTT):c.1378C>T (p.Arg460Trp)	not specified [RCV004198863]	uncertain significance	10	96335909	96335909	Human		name
156054359	CV2388602	single nucleotide variant	NM_004088.4(DNTT):c.1358G>A (p.Arg453Gln)	not specified [RCV004239486]	uncertain significance	10	96332595	96332595	Human		name
401781335	CV2681970	single nucleotide variant	NM_004088.4(DNTT):c.1466G>A (p.Ser489Asn)	not specified [RCV004296952]	uncertain significance	10	96338160	96338160	Human		name
401749958	CV2719461	single nucleotide variant	NM_004088.4(DNTT):c.1421A>C (p.His474Pro)	not specified [RCV004326860]	uncertain significance	10	96335952	96335952	Human		name
401761720	CV2726878	single nucleotide variant	NM_004088.4(DNTT):c.1408A>T (p.Ile470Phe)	not specified [RCV004323171]	uncertain significance	10	96335939	96335939	Human		name
401866566	CV2782880	single nucleotide variant	NM_004088.4(DNTT):c.1450T>C (p.Phe484Leu)	not specified [RCV004361684]	uncertain significance	10	96338144	96338144	Human		name
401882940	CV2788684	single nucleotide variant	NM_004088.4(DNTT):c.1196A>G (p.His399Arg)	not specified [RCV004361163]	uncertain significance	10	96332433	96332433	Human		name
405749133	CV3241101	single nucleotide variant	NM_004088.4(DNTT):c.1132G>C (p.Asp378His)	not specified [RCV004381704]	uncertain significance	10	96332369	96332369	Human		name
405749994	CV3241102	single nucleotide variant	NM_004088.4(DNTT):c.1348A>T (p.Thr450Ser)	not specified [RCV004381705]	uncertain significance	10	96332585	96332585	Human		name
405749146	CV3241103	single nucleotide variant	NM_004088.4(DNTT):c.1396G>A (p.Glu466Lys)	not specified [RCV004381706]	uncertain significance	10	96335927	96335927	Human		name
405749159	CV3241105	single nucleotide variant	NM_004088.4(DNTT):c.1435A>G (p.Lys479Glu)	not specified [RCV004381708]	uncertain significance	10	96335966	96335966	Human		name
407505417	CV3437710	single nucleotide variant	NM_004088.4(DNTT):c.1117T>G (p.Leu373Val)	not specified [RCV004624353]	uncertain significance	10	96332354	96332354	Human		name
597660824	CV3659388	single nucleotide variant	NM_004088.4(DNTT):c.1414G>A (p.Asp472Asn)	not specified [RCV004911806]	uncertain significance	10	96335945	96335945	Human		name
597660807	CV3659390	single nucleotide variant	NM_004088.4(DNTT):c.1286C>T (p.Ala429Val)	not specified [RCV004911808]	uncertain significance	10	96332523	96332523	Human		name
598174227	CV3964342	single nucleotide variant	NM_004088.4(DNTT):c.1325G>T (p.Arg442Leu)	not specified [RCV005331661]	uncertain significance	10	96332562	96332562	Human		name
598174234	CV3964343	single nucleotide variant	NM_004088.4(DNTT):c.1322G>A (p.Arg441His)	not specified [RCV005331662]	uncertain significance	10	96332559	96332559	Human		name
598174274	CV3964348	single nucleotide variant	NM_004088.4(DNTT):c.1382G>T (p.Arg461Leu)	not specified [RCV005331667]	uncertain significance	10	96335913	96335913	Human		name
8633800	CV89016	single nucleotide variant	NM_001017520.1(DNTT):c.661G>A (p.Val221Met)	Malignant melanoma [RCV000069113]	not provided	10	96320771	96320771	Human		name
405749206	CV3241112	single nucleotide variant	NM_052951.3(DNTTIP1):c.11C>G (p.Thr4Ser)	not specified [RCV004381715]	uncertain significance	20	45792015	45792015	Human		name
407505431	CV3437714	single nucleotide variant	NM_052951.3(DNTTIP1):c.19G>A (p.Ala7Thr)	not specified [RCV004624357]	uncertain significance	20	45792023	45792023	Human		name
597660782	CV3659393	single nucleotide variant	NM_052951.3(DNTTIP1):c.17A>G (p.Asp6Gly)	not specified [RCV004911811]	uncertain significance	20	45792021	45792021	Human		name
598174295	CV3964351	single nucleotide variant	NM_052951.3(DNTTIP1):c.26A>C (p.Gln9Pro)	not specified [RCV005331670]	uncertain significance	20	45792030	45792030	Human		name
156304443	CV2304775	single nucleotide variant	NM_014597.5(DNTTIP2):c.71A>G (p.Lys24Arg)	not specified [RCV004166918]	uncertain significance	1	93879078	93879078	Human		name
401772021	CV2712039	single nucleotide variant	NM_014597.5(DNTTIP2):c.34A>C (p.Ser12Arg)	not specified [RCV004311458]	uncertain significance	1	93879115	93879115	Human		name
405749336	CV3237672	single nucleotide variant	NM_014597.5(DNTTIP2):c.77T>C (p.Phe26Ser)	not specified [RCV004381734]	likely benign	1	93877858	93877858	Human		name
598174302	CV3964352	single nucleotide variant	NM_052951.3(DNTTIP1):c.59G>T (p.Gly20Val)	not specified [RCV005331671]	uncertain significance	20	45792063	45792063	Human		name
156236839	CV2224158	single nucleotide variant	NM_052951.3(DNTTIP1):c.287C>G (p.Ala96Gly)	not specified [RCV004096011]	uncertain significance	20	45795358	45795358	Human		name
155971131	CV2335656	single nucleotide variant	NM_052951.3(DNTTIP1):c.180C>A (p.Phe60Leu)	not specified [RCV004193857]	uncertain significance	20	45793924	45793924	Human		name
156133657	CV2382996	single nucleotide variant	NM_052951.3(DNTTIP1):c.286G>A (p.Ala96Thr)	not specified [RCV004217581]	uncertain significance	20	45795357	45795357	Human		name
401760179	CV2718743	single nucleotide variant	NM_014597.5(DNTTIP2):c.221C>T (p.Ser74Leu)	not specified [RCV004328496]	uncertain significance	1	93877714	93877714	Human		name
405749304	CV3237667	single nucleotide variant	NM_014597.5(DNTTIP2):c.210A>T (p.Arg70Ser)	not specified [RCV004381729]	uncertain significance	1	93877725	93877725	Human		name
405749213	CV3241113	single nucleotide variant	NM_052951.3(DNTTIP1):c.238G>C (p.Glu80Gln)	not specified [RCV004381716]	uncertain significance	20	45793982	45793982	Human		name
407505433	CV3437715	single nucleotide variant	NM_052951.3(DNTTIP1):c.289G>A (p.Ala97Thr)	not specified [RCV004624358]	uncertain significance	20	45795360	45795360	Human		name
407505446	CV3437719	single nucleotide variant	NM_014597.5(DNTTIP2):c.127G>T (p.Ala43Ser)	not specified [RCV004624362]	uncertain significance	1	93877808	93877808	Human		name
597734006	CV3659394	single nucleotide variant	NM_014597.5(DNTTIP2):c.292G>A (p.Glu98Lys)	not specified [RCV004920187]	uncertain significance	1	93877643	93877643	Human		name
598174290	CV3964350	single nucleotide variant	NM_052951.3(DNTTIP1):c.261C>A (p.Asn87Lys)	not specified [RCV005331669]	uncertain significance	20	45794005	45794005	Human		name
156182238	CV2201874	single nucleotide variant	NM_014597.5(DNTTIP2):c.598A>C (p.Thr200Pro)	not specified [RCV004082300]	uncertain significance	1	93877337	93877337	Human		name
156248178	CV2203056	single nucleotide variant	NM_014597.5(DNTTIP2):c.584T>C (p.Phe195Ser)	not specified [RCV004069307]	uncertain significance	1	93877351	93877351	Human		name
155970367	CV2241369	single nucleotide variant	NM_014597.5(DNTTIP2):c.976C>T (p.Leu326Phe)	not specified [RCV004102503]	uncertain significance	1	93876959	93876959	Human		name
156038373	CV2332623	single nucleotide variant	NM_052951.3(DNTTIP1):c.539G>A (p.Arg180Gln)	not specified [RCV004189303]	uncertain significance	20	45802039	45802039	Human		name
156305877	CV2338946	single nucleotide variant	NM_052951.3(DNTTIP1):c.864T>A (p.Asp288Glu)	not specified [RCV004184535]	uncertain significance	20	45811069	45811069	Human		name
156100243	CV2367498	single nucleotide variant	NM_014597.5(DNTTIP2):c.518A>G (p.Asp173Gly)	not specified [RCV004211435]	uncertain significance	1	93877417	93877417	Human		name
401737000	CV2699647	single nucleotide variant	NM_014597.5(DNTTIP2):c.775A>G (p.Asn259Asp)	not specified [RCV004299829]	uncertain significance	1	93877160	93877160	Human		name
401762450	CV2723447	single nucleotide variant	NM_052951.3(DNTTIP1):c.527T>C (p.Leu176Pro)	not specified [RCV004323521]	uncertain significance	20	45802027	45802027	Human		name
401859325	CV2771532	single nucleotide variant	NM_052951.3(DNTTIP1):c.598C>G (p.Pro200Ala)	not specified [RCV004348562]	uncertain significance	20	45803373	45803373	Human		name
401879545	CV2785239	single nucleotide variant	NM_014597.5(DNTTIP2):c.623G>C (p.Arg208Thr)	not specified [RCV004357008]	uncertain significance	1	93877312	93877312	Human		name
405749999	CV3237668	single nucleotide variant	NM_014597.5(DNTTIP2):c.361A>G (p.Ser121Gly)	not specified [RCV004381730]	uncertain significance	1	93877574	93877574	Human		name
405749318	CV3237669	single nucleotide variant	NM_014597.5(DNTTIP2):c.580T>G (p.Ser194Ala)	not specified [RCV004381731]	uncertain significance	1	93877355	93877355	Human		name
405749332	CV3237671	single nucleotide variant	NM_014597.5(DNTTIP2):c.598A>G (p.Thr200Ala)	not specified [RCV004381733]	uncertain significance	1	93877337	93877337	Human		name
405749344	CV3237673	single nucleotide variant	NM_014597.5(DNTTIP2):c.809C>T (p.Ser270Phe)	not specified [RCV004381735]	likely benign	1	93877126	93877126	Human		name
405749351	CV3237674	single nucleotide variant	NM_014597.5(DNTTIP2):c.844G>A (p.Glu282Lys)	not specified [RCV004381736]	likely benign	1	93877091	93877091	Human		name
405749221	CV3241114	single nucleotide variant	NM_052951.3(DNTTIP1):c.328G>A (p.Ala110Thr)	not specified [RCV004381717]	likely benign	20	45795399	45795399	Human		name
405749227	CV3241115	single nucleotide variant	NM_052951.3(DNTTIP1):c.473A>C (p.His158Pro)	not specified [RCV004381718]	uncertain significance	20	45801433	45801433	Human		name
407505427	CV3437713	single nucleotide variant	NM_052951.3(DNTTIP1):c.961C>T (p.Arg321Cys)	not specified [RCV004624356]	uncertain significance	20	45811166	45811166	Human		name
407505440	CV3437717	single nucleotide variant	NM_014597.5(DNTTIP2):c.749G>T (p.Arg250Ile)	not specified [RCV004624360]	uncertain significance	1	93877186	93877186	Human		name
597660799	CV3659391	single nucleotide variant	NM_052951.3(DNTTIP1):c.426G>C (p.Glu142Asp)	not specified [RCV004911809]	uncertain significance	20	45801127	45801127	Human		name
597660766	CV3659397	single nucleotide variant	NM_014597.5(DNTTIP2):c.842A>T (p.His281Leu)	not specified [RCV004911813]	uncertain significance	1	93877093	93877093	Human		name
156387860	CV2221636	single nucleotide variant	NM_014597.5(DNTTIP2):c.1483C>A (p.Pro495Thr)	not specified [RCV004096884]	uncertain significance	1	93876452	93876452	Human		name
156025676	CV2242265	single nucleotide variant	NM_014597.5(DNTTIP2):c.1940G>C (p.Gly647Ala)	not specified [RCV004111289]	uncertain significance	1	93872199	93872199	Human		name
156114669	CV2268630	single nucleotide variant	NM_014597.5(DNTTIP2):c.1790A>C (p.Glu597Ala)	not specified [RCV004124038]	uncertain significance	1	93875661	93875661	Human		name
155905806	CV2303184	single nucleotide variant	NM_014597.5(DNTTIP2):c.1961C>G (p.Thr654Arg)	not specified [RCV004156947]	uncertain significance	1	93872178	93872178	Human		name
156266343	CV2312331	single nucleotide variant	NM_014597.5(DNTTIP2):c.1576G>A (p.Glu526Lys)	not specified [RCV004167037]	uncertain significance	1	93876359	93876359	Human		name
156362511	CV2330225	single nucleotide variant	NM_014597.5(DNTTIP2):c.1334T>G (p.Leu445Arg)	not specified [RCV004187683]	uncertain significance	1	93876601	93876601	Human		name
329367660	CV2427494	single nucleotide variant	NM_014597.5(DNTTIP2):c.1898G>A (p.Arg633His)	not specified [RCV004250133]	uncertain significance	1	93873123	93873123	Human		name
329377485	CV2453389	single nucleotide variant	NM_014597.5(DNTTIP2):c.2165C>G (p.Ser722Cys)	not specified [RCV004267006]	uncertain significance	1	93870695	93870695	Human		name
329394680	CV2461520	single nucleotide variant	NM_014597.5(DNTTIP2):c.1364A>T (p.Asn455Ile)	not specified [RCV004269441]	uncertain significance	1	93876571	93876571	Human		name
401731071	CV2674250	single nucleotide variant	NM_014597.5(DNTTIP2):c.1375G>A (p.Glu459Lys)	not specified [RCV004289136]	uncertain significance	1	93876560	93876560	Human		name
401757008	CV2678181	single nucleotide variant	NM_014597.5(DNTTIP2):c.1822G>A (p.Val608Ile)	not specified [RCV004296689]	likely benign	1	93873199	93873199	Human		name
401759597	CV2701627	single nucleotide variant	NM_014597.5(DNTTIP2):c.2080G>C (p.Val694Leu)	not specified [RCV004314046]	uncertain significance	1	93870780	93870780	Human		name
401874916	CV2781162	single nucleotide variant	NM_014597.5(DNTTIP2):c.1121G>T (p.Arg374Ile)	not specified [RCV004352212]	uncertain significance	1	93876814	93876814	Human		name
405749254	CV3237660	single nucleotide variant	NM_014597.5(DNTTIP2):c.1235T>C (p.Met412Thr)	not specified [RCV004381722]	uncertain significance	1	93876700	93876700	Human		name
405749262	CV3237661	single nucleotide variant	NM_014597.5(DNTTIP2):c.1338C>G (p.Ser446Arg)	not specified [RCV004381723]	uncertain significance	1	93876597	93876597	Human		name
405749268	CV3237662	single nucleotide variant	NM_014597.5(DNTTIP2):c.1505A>C (p.Asn502Thr)	not specified [RCV004381724]	uncertain significance	1	93876430	93876430	Human		name
405749274	CV3237663	single nucleotide variant	NM_014597.5(DNTTIP2):c.1529A>G (p.Lys510Arg)	not specified [RCV004381725]	uncertain significance	1	93876406	93876406	Human		name
405749280	CV3237664	single nucleotide variant	NM_014597.5(DNTTIP2):c.1609G>A (p.Glu537Lys)	not specified [RCV004381726]	uncertain significance	1	93876326	93876326	Human		name
405749290	CV3237665	single nucleotide variant	NM_014597.5(DNTTIP2):c.1993A>G (p.Lys665Glu)	not specified [RCV004381727]	uncertain significance	1	93872146	93872146	Human		name
405749240	CV3241117	single nucleotide variant	NM_014597.5(DNTTIP2):c.1040C>T (p.Ala347Val)	not specified [RCV004381720]	uncertain significance	1	93876895	93876895	Human		name
405749246	CV3241118	single nucleotide variant	NM_014597.5(DNTTIP2):c.1192G>A (p.Asp398Asn)	not specified [RCV004381721]	uncertain significance	1	93876743	93876743	Human		name
407505443	CV3437718	single nucleotide variant	NM_014597.5(DNTTIP2):c.1721G>A (p.Gly574Asp)	not specified [RCV004624361]	uncertain significance	1	93875730	93875730	Human		name
407505449	CV3437720	single nucleotide variant	NM_014597.5(DNTTIP2):c.1036A>C (p.Asn346His)	not specified [RCV004624363]	uncertain significance	1	93876899	93876899	Human		name
407505453	CV3437721	single nucleotide variant	NM_014597.5(DNTTIP2):c.1957A>G (p.Met653Val)	not specified [RCV004624364]	uncertain significance	1	93872182	93872182	Human		name
597734012	CV3659395	single nucleotide variant	NM_014597.5(DNTTIP2):c.1688G>T (p.Ser563Ile)	not specified [RCV004920188]	uncertain significance	1	93875763	93875763	Human		name
597660774	CV3659396	single nucleotide variant	NM_014597.5(DNTTIP2):c.1946A>C (p.Lys649Thr)	not specified [RCV004911812]	uncertain significance	1	93872193	93872193	Human		name
597660759	CV3659398	single nucleotide variant	NM_014597.5(DNTTIP2):c.2047G>A (p.Gly683Ser)	not specified [RCV004911814]	uncertain significance	1	93872092	93872092	Human		name
597660752	CV3659399	single nucleotide variant	NM_014597.5(DNTTIP2):c.1021A>G (p.Thr341Ala)	not specified [RCV004911815]	uncertain significance	1	93876914	93876914	Human		name
597660744	CV3659400	single nucleotide variant	NM_014597.5(DNTTIP2):c.1339A>G (p.Ser447Gly)	not specified [RCV004911816]	uncertain significance	1	93876596	93876596	Human		name
598174308	CV3964353	single nucleotide variant	NM_014597.5(DNTTIP2):c.1655C>T (p.Thr552Ile)	not specified [RCV005331672]	uncertain significance	1	93876280	93876280	Human		name
598174323	CV3964355	single nucleotide variant	NM_014597.5(DNTTIP2):c.1055C>T (p.Ser352Phe)	not specified [RCV005331674]	uncertain significance	1	93876880	93876880	Human		name
598174330	CV3964356	single nucleotide variant	NM_014597.5(DNTTIP2):c.1003G>A (p.Val335Ile)	not specified [RCV005331675]	uncertain significance	1	93876932	93876932	Human		name
598174336	CV3964357	single nucleotide variant	NM_014597.5(DNTTIP2):c.1136A>G (p.Lys379Arg)	not specified [RCV005331676]	likely benign	1	93876799	93876799	Human		name
598174344	CV3964358	single nucleotide variant	NM_014597.5(DNTTIP2):c.1291C>T (p.Pro431Ser)	not specified [RCV005331677]	uncertain significance	1	93876644	93876644	Human		name
598174351	CV3964359	single nucleotide variant	NM_014597.5(DNTTIP2):c.1910G>A (p.Arg637Gln)	not specified [RCV005331678]	uncertain significance	1	93872229	93872229	Human		name
598174359	CV3964360	single nucleotide variant	NM_014597.5(DNTTIP2):c.2089C>T (p.Pro697Ser)	not specified [RCV005331679]	uncertain significance	1	93870771	93870771	Human		name

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