Ankrd16 Variant Search Result - Rat Genome Database

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47 records found for search term Ankrd16

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156117378	CV2231863	single nucleotide variant	NM_019046.3(ANKRD16):c.20C>T (p.Pro7Leu)	not specified [RCV004098662]	uncertain significance	10	5889335	5889335	Human		name
598236809	CV3984503	single nucleotide variant	NM_019046.3(ANKRD16):c.25C>A (p.Arg9Ser)	not specified [RCV005363945]	uncertain significance	10	5889330	5889330	Human		name
401779452	CV2731830	single nucleotide variant	NM_019046.3(ANKRD16):c.40G>A (p.Val14Met)	not specified [RCV004333083]	uncertain significance	10	5889315	5889315	Human		name
597649250	CV3703199	single nucleotide variant	NM_019046.3(ANKRD16):c.984G>A (p.Gln328=)	not specified [RCV004942881]	likely benign	10	5878232	5878232	Human		name
598260314	CV3984513	single nucleotide variant	NM_019046.3(ANKRD16):c.80A>T (p.Gln27Leu)	not specified [RCV005347597]	uncertain significance	10	5889275	5889275	Human		name
598236851	CV3984523	single nucleotide variant	NM_019046.3(ANKRD16):c.61G>T (p.Ala21Ser)	not specified [RCV005363953]	uncertain significance	10	5889294	5889294	Human		name
598236901	CV3984551	single nucleotide variant	NM_019046.3(ANKRD16):c.969C>G (p.Ala323=)	not specified [RCV005363964]	likely benign	10	5878247	5878247	Human		name
155916629	CV2197522	single nucleotide variant	NM_019046.3(ANKRD16):c.118C>G (p.Leu40Val)	not specified [RCV004081246]	uncertain significance	10	5889237	5889237	Human		name
156089870	CV2206527	single nucleotide variant	NM_019046.3(ANKRD16):c.127T>C (p.Cys43Arg)	not specified [RCV004080879]	uncertain significance	10	5889228	5889228	Human		name
155968334	CV2217007	single nucleotide variant	NM_019046.3(ANKRD16):c.106G>A (p.Ala36Thr)	not specified [RCV004085365]	uncertain significance	10	5889249	5889249	Human		name
156244837	CV2231634	single nucleotide variant	NM_019046.3(ANKRD16):c.228C>G (p.His76Gln)	not specified [RCV004098206]	uncertain significance	10	5889127	5889127	Human		name
156182190	CV2288232	single nucleotide variant	NM_019046.3(ANKRD16):c.277C>T (p.Arg93Trp)	not specified [RCV004149743]	uncertain significance	10	5889078	5889078	Human		name
401745130	CV2681196	single nucleotide variant	NM_019046.3(ANKRD16):c.281G>A (p.Gly94Glu)	not specified [RCV004289338]	uncertain significance	10	5889074	5889074	Human		name
405811762	CV3285095	single nucleotide variant	NM_019046.3(ANKRD16):c.104C>G (p.Pro35Arg)	not specified [RCV004408631]	uncertain significance	10	5889251	5889251	Human		name
407506998	CV3447297	single nucleotide variant	NM_019046.3(ANKRD16):c.154G>T (p.Val52Leu)	not specified [RCV004646640]	uncertain significance	10	5889201	5889201	Human		name
597649310	CV3703206	single nucleotide variant	NM_019046.3(ANKRD16):c.100G>C (p.Gly34Arg)	not specified [RCV004942888]	uncertain significance	10	5889255	5889255	Human		name
597649780	CV3703292	single nucleotide variant	NM_019046.3(ANKRD16):c.112G>A (p.Asp38Asn)	not specified [RCV004942941]	uncertain significance	10	5889243	5889243	Human		name
598230031	CV3984543	single nucleotide variant	NM_019046.3(ANKRD16):c.103C>T (p.Pro35Ser)	not specified [RCV005362641]	uncertain significance	10	5889252	5889252	Human		name
156033205	CV2214612	single nucleotide variant	NM_019046.3(ANKRD16):c.802G>A (p.Val268Met)	not specified [RCV004090446]	uncertain significance	10	5883053	5883053	Human		name
156207532	CV2250047	single nucleotide variant	NM_019046.3(ANKRD16):c.622G>C (p.Ala208Pro)	not specified [RCV004116874]	likely benign	10	5884034	5884034	Human		name
156203588	CV2300742	single nucleotide variant	NM_019046.3(ANKRD16):c.626T>C (p.Leu209Ser)	not specified [RCV004155676]	uncertain significance	10	5884030	5884030	Human		name
156007630	CV2389990	single nucleotide variant	NM_019046.3(ANKRD16):c.310G>A (p.Asp104Asn)	not specified [RCV004238607]	uncertain significance	10	5889045	5889045	Human		name
329382293	CV2438698	single nucleotide variant	NM_019046.3(ANKRD16):c.437G>A (p.Arg146Gln)	not specified [RCV004261852]	uncertain significance	10	5887945	5887945	Human		name
401742676	CV2677652	single nucleotide variant	NM_019046.3(ANKRD16):c.655G>A (p.Asp219Asn)	not specified [RCV004291738]	uncertain significance	10	5884001	5884001	Human		name
401731460	CV2701376	single nucleotide variant	NM_019046.3(ANKRD16):c.676G>A (p.Asp226Asn)	not specified [RCV004311744]	uncertain significance	10	5883980	5883980	Human		name
401779457	CV2731831	single nucleotide variant	NM_019046.3(ANKRD16):c.542A>G (p.His181Arg)	not specified [RCV004333084]	uncertain significance	10	5885759	5885759	Human		name
401878820	CV2754838	single nucleotide variant	NM_019046.3(ANKRD16):c.530C>T (p.Thr177Ile)	not specified [RCV004341315]	uncertain significance	10	5887852	5887852	Human		name
401881789	CV2783958	single nucleotide variant	NM_019046.3(ANKRD16):c.457C>T (p.Leu153Phe)	not specified [RCV004362377]	uncertain significance	10	5887925	5887925	Human		name
405811811	CV3285118	single nucleotide variant	NM_019046.3(ANKRD16):c.328A>T (p.Met110Leu)	not specified [RCV004408654]	uncertain significance	10	5888054	5888054	Human		name
405811845	CV3285134	single nucleotide variant	NM_019046.3(ANKRD16):c.503G>A (p.Ser168Asn)	not specified [RCV004408670]	uncertain significance	10	5887879	5887879	Human		name
405811862	CV3285142	single nucleotide variant	NM_019046.3(ANKRD16):c.616G>A (p.Val206Ile)	not specified [RCV004408678]	uncertain significance	10	5884040	5884040	Human		name
405811873	CV3285147	single nucleotide variant	NM_019046.3(ANKRD16):c.619A>G (p.Thr207Ala)	not specified [RCV004408683]	uncertain significance	10	5884037	5884037	Human		name
405811879	CV3285150	single nucleotide variant	NM_019046.3(ANKRD16):c.622G>A (p.Ala208Thr)	not specified [RCV004408686]	uncertain significance	10	5884034	5884034	Human		name
405811914	CV3285166	single nucleotide variant	NM_019046.3(ANKRD16):c.880T>G (p.Leu294Val)	not specified [RCV004408702]	uncertain significance	10	5880346	5880346	Human		name
407507033	CV3447319	single nucleotide variant	NM_019046.3(ANKRD16):c.700G>T (p.Ala234Ser)	not specified [RCV004646654]	uncertain significance	10	5883155	5883155	Human		name
597649560	CV3703235	single nucleotide variant	NM_019046.3(ANKRD16):c.790G>A (p.Val264Ile)	not specified [RCV004942916]	likely benign	10	5883065	5883065	Human		name
597649569	CV3703256	single nucleotide variant	NM_019046.3(ANKRD16):c.302A>G (p.Lys101Arg)	not specified [RCV004942917]	uncertain significance	10	5889053	5889053	Human		name
597649579	CV3703266	single nucleotide variant	NM_019046.3(ANKRD16):c.492G>C (p.Trp164Cys)	not specified [RCV004942918]	uncertain significance	10	5887890	5887890	Human		name
597649678	CV3703277	single nucleotide variant	NM_019046.3(ANKRD16):c.352G>A (p.Gly118Arg)	not specified [RCV004942929]	uncertain significance	10	5888030	5888030	Human		name
597649723	CV3703283	single nucleotide variant	NM_019046.3(ANKRD16):c.794A>G (p.Asp265Gly)	not specified [RCV004942934]	uncertain significance	10	5883061	5883061	Human		name
598236930	CV3984561	single nucleotide variant	NM_019046.3(ANKRD16):c.563A>G (p.Lys188Arg)	not specified [RCV005363970]	uncertain significance	10	5885738	5885738	Human		name
598236960	CV3984571	single nucleotide variant	NM_019046.3(ANKRD16):c.604G>A (p.Asp202Asn)	not specified [RCV005363977]	uncertain significance	10	5884052	5884052	Human		name
155984021	CV2247716	single nucleotide variant	NM_019046.3(ANKRD16):c.1034T>A (p.Leu345His)	not specified [RCV004119403]	uncertain significance	10	5878182	5878182	Human		name
401782366	CV2686753	single nucleotide variant	NM_019046.3(ANKRD16):c.1016G>T (p.Gly339Val)	not specified [RCV004301942]	uncertain significance	10	5878200	5878200	Human		name
407475767	CV3447308	single nucleotide variant	NM_019046.3(ANKRD16):c.1039A>G (p.Arg347Gly)	not specified [RCV004638427]	uncertain significance	10	5878177	5878177	Human		name
597649409	CV3703217	single nucleotide variant	NM_019046.3(ANKRD16):c.1075G>A (p.Ala359Thr)	not specified [RCV004942899]	uncertain significance	10	5878141	5878141	Human		name
598230006	CV3984534	single nucleotide variant	NM_019046.3(ANKRD16):c.1078A>G (p.Met360Val)	not specified [RCV005362637]	uncertain significance	10	5878138	5878138	Human		name

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