Aplf Variant Search Result - Rat Genome Database

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48 records found for search term Aplf

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8577390	CV111765	single nucleotide variant	NM_173545.2(APLF):c.805-4097G>C	Lung cancer [RCV000092288]	uncertain significance	2	68533775	68533775	Human		name
407512003	CV3463581	single nucleotide variant	NM_173545.3(APLF):c.25C>T (p.Pro9Ser)	not specified [RCV004648240]	uncertain significance	2	68467756	68467756	Human		name
156140499	CV2247075	single nucleotide variant	NM_173545.3(APLF):c.29G>T (p.Arg10Leu)	not specified [RCV004114621]	uncertain significance	2	68467760	68467760	Human		name
329361507	CV2459780	single nucleotide variant	NM_173545.3(APLF):c.75C>G (p.Ile25Met)	not specified [RCV004277194]	uncertain significance	2	68467806	68467806	Human		name
407511990	CV3463571	single nucleotide variant	NM_173545.3(APLF):c.55G>A (p.Ala19Thr)	not specified [RCV004648235]	uncertain significance	2	68467786	68467786	Human		name
155916126	CV2281930	single nucleotide variant	NM_173545.3(APLF):c.221C>T (p.Pro74Leu)	not specified [RCV004138704]	uncertain significance	2	68502783	68502783	Human		name
405662126	CV3289717	single nucleotide variant	NM_173545.3(APLF):c.160A>G (p.Ile54Val)	not specified [RCV004417660]	uncertain significance	2	68490253	68490253	Human		name
405662129	CV3289718	single nucleotide variant	NM_173545.3(APLF):c.200C>T (p.Ser67Leu)	not specified [RCV004417661]	uncertain significance	2	68502762	68502762	Human		name
405662132	CV3289719	single nucleotide variant	NM_173545.3(APLF):c.244T>C (p.Tyr82His)	not specified [RCV004417662]	uncertain significance	2	68502806	68502806	Human		name
405662135	CV3289720	single nucleotide variant	NM_173545.3(APLF):c.295C>T (p.Arg99Cys)	not specified [RCV004417663]	likely benign	2	68502857	68502857	Human		name
405662138	CV3289721	single nucleotide variant	NM_173545.3(APLF):c.296G>A (p.Arg99His)	not specified [RCV004417664]	uncertain significance	2	68502858	68502858	Human		name
597715212	CV3574848	single nucleotide variant	NM_173545.3(APLF):c.212A>T (p.Gln71Leu)	not specified [RCV004841313]	uncertain significance	2	68502774	68502774	Human		name
597715460	CV3574880	single nucleotide variant	NM_173545.3(APLF):c.1326G>A (p.Thr442=)	not specified [RCV004841337]	likely benign	2	68567380	68567380	Human		name
598242488	CV4005311	single nucleotide variant	NM_173545.3(APLF):c.212A>G (p.Gln71Arg)	not specified [RCV005383441]	uncertain significance	2	68502774	68502774	Human		name
156232942	CV2197085	single nucleotide variant	NM_173545.3(APLF):c.524A>G (p.Gln175Arg)	not specified [RCV004071522]	uncertain significance	2	68513582	68513582	Human		name
156286521	CV2292090	single nucleotide variant	NM_173545.3(APLF):c.598C>G (p.Leu200Val)	not specified [RCV004160359]	uncertain significance	2	68513656	68513656	Human		name
156202638	CV2313237	single nucleotide variant	NM_173545.3(APLF):c.439G>A (p.Glu147Lys)	not specified [RCV004161489]	uncertain significance	2	68513177	68513177	Human		name
156269794	CV2315062	single nucleotide variant	NM_173545.3(APLF):c.755G>A (p.Gly252Glu)	not specified [RCV004164970]	uncertain significance	2	68526193	68526193	Human		name
156199423	CV2331316	single nucleotide variant	NM_173545.3(APLF):c.545G>A (p.Arg182Lys)	not specified [RCV004183960]	uncertain significance	2	68513603	68513603	Human		name
329381973	CV2424284	single nucleotide variant	NM_173545.3(APLF):c.578A>G (p.Glu193Gly)	not specified [RCV004252193]	uncertain significance	2	68513636	68513636	Human		name
401741922	CV2697658	single nucleotide variant	NM_173545.3(APLF):c.400A>T (p.Ile134Phe)	not specified [RCV004300402]	uncertain significance	2	68513138	68513138	Human		name
401745040	CV2698452	single nucleotide variant	NM_173545.3(APLF):c.894A>G (p.Ile298Met)	not specified [RCV004298963]	uncertain significance	2	68537961	68537961	Human		name
401770066	CV2719020	single nucleotide variant	NM_173545.3(APLF):c.890C>T (p.Pro297Leu)	not specified [RCV004322606]	uncertain significance	2	68537957	68537957	Human		name
405662141	CV3289722	single nucleotide variant	NM_173545.3(APLF):c.382A>T (p.Thr128Ser)	not specified [RCV004417665]	uncertain significance	2	68513120	68513120	Human		name
405662146	CV3289723	single nucleotide variant	NM_173545.3(APLF):c.446G>T (p.Ser149Ile)	not specified [RCV004417666]	uncertain significance	2	68513184	68513184	Human		name
405662148	CV3289724	single nucleotide variant	NM_173545.3(APLF):c.505A>G (p.Asn169Asp)	not specified [RCV004417667]	uncertain significance	2	68513563	68513563	Human		name
405662151	CV3289725	single nucleotide variant	NM_173545.3(APLF):c.640A>G (p.Ser214Gly)	not specified [RCV004417668]	uncertain significance	2	68526078	68526078	Human		name
405662153	CV3289726	single nucleotide variant	NM_173545.3(APLF):c.754G>A (p.Gly252Arg)	not specified [RCV004417669]	uncertain significance	2	68526192	68526192	Human		name
405662155	CV3289727	single nucleotide variant	NM_173545.3(APLF):c.997G>C (p.Gly333Arg)	not specified [RCV004417670]	uncertain significance	2	68538064	68538064	Human		name
597715022	CV3574826	single nucleotide variant	NM_173545.3(APLF):c.944C>G (p.Pro315Arg)	not specified [RCV004841296]	uncertain significance	2	68538011	68538011	Human		name
597715134	CV3574837	single nucleotide variant	NM_173545.3(APLF):c.934A>G (p.Lys312Glu)	not specified [RCV004841306]	uncertain significance	2	68538001	68538001	Human		name
597715289	CV3574859	single nucleotide variant	NM_173545.3(APLF):c.460A>G (p.Lys154Glu)	not specified [RCV004841321]	uncertain significance	2	68513198	68513198	Human		name
597715374	CV3574870	single nucleotide variant	NM_173545.3(APLF):c.689A>G (p.Gln230Arg)	not specified [RCV004841329]	uncertain significance	2	68526127	68526127	Human		name
598183042	CV4005321	single nucleotide variant	NM_173545.3(APLF):c.466C>G (p.Gln156Glu)	not specified [RCV005395238]	uncertain significance	2	68513204	68513204	Human		name
598242624	CV4005341	single nucleotide variant	NM_173545.3(APLF):c.385C>T (p.Pro129Ser)	not specified [RCV005383466]	uncertain significance	2	68513123	68513123	Human		name
156147576	CV2212843	single nucleotide variant	NM_173545.3(APLF):c.1228G>C (p.Val410Leu)	not specified [RCV004091513]	uncertain significance	2	68545254	68545254	Human		name
156042173	CV2215746	single nucleotide variant	NM_173545.3(APLF):c.1349A>G (p.Asp450Gly)	not specified [RCV004095354]	uncertain significance	2	68577835	68577835	Human		name
156208308	CV2250109	single nucleotide variant	NM_173545.3(APLF):c.1279T>C (p.Cys427Arg)	not specified [RCV004116926]	uncertain significance	2	68545305	68545305	Human		name
156367494	CV2266807	single nucleotide variant	NM_173545.3(APLF):c.1016A>G (p.Glu339Gly)	not specified [RCV004137623]	uncertain significance	2	68538083	68538083	Human		name
155941513	CV2300855	single nucleotide variant	NM_173545.3(APLF):c.1274C>T (p.Pro425Leu)	not specified [RCV004158060]	uncertain significance	2	68545300	68545300	Human		name
329374422	CV2463546	single nucleotide variant	NM_173545.3(APLF):c.1040C>T (p.Ser347Phe)	not specified [RCV004277357]	uncertain significance	2	68538107	68538107	Human		name
405662123	CV3289716	single nucleotide variant	NM_173545.3(APLF):c.1228G>A (p.Val410Met)	not specified [RCV004417659]	likely benign	2	68545254	68545254	Human		name
407512015	CV3463591	single nucleotide variant	NM_173545.3(APLF):c.1403T>C (p.Phe468Ser)	not specified [RCV004648245]	uncertain significance	2	68577889	68577889	Human		name
407530756	CV3463600	single nucleotide variant	NM_173545.3(APLF):c.1334T>G (p.Val445Gly)	not specified [RCV004657221]	uncertain significance	2	68577820	68577820	Human		name
597696610	CV3574815	single nucleotide variant	NM_173545.3(APLF):c.1252C>T (p.Arg418Trp)	not specified [RCV004839230]	uncertain significance	2	68545278	68545278	Human		name
597715559	CV3574891	single nucleotide variant	NM_173545.3(APLF):c.1000G>A (p.Asp334Asn)	not specified [RCV004841346]	uncertain significance	2	68538067	68538067	Human		name
597715597	CV3574895	single nucleotide variant	NM_173545.3(APLF):c.1078A>G (p.Lys360Glu)	not specified [RCV004841349]	uncertain significance	2	68538145	68538145	Human		name
598183059	CV4005332	single nucleotide variant	NM_173545.3(APLF):c.1325C>A (p.Thr442Lys)	not specified [RCV005395241]	uncertain significance	2	68567379	68567379	Human		name

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