Slc37a2 Variant Search Result - Rat Genome Database

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54 records found for search term Slc37a2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401778676	CV2705486	single nucleotide variant	NM_001145290.2(SLC37A2):c.1490+205C>T	not specified [RCV004316576]	uncertain significance	11	125086223	125086223	Human		name
156210718	CV2314337	single nucleotide variant	NM_001145290.2(SLC37A2):c.52G>A (p.Asp18Asn)	not specified [RCV004166680]	uncertain significance	11	125063419	125063419	Human		name
155928191	CV2361878	single nucleotide variant	NM_001145290.2(SLC37A2):c.37C>T (p.Arg13Trp)	not specified [RCV004207653]	uncertain significance	11	125063404	125063404	Human		name
401910267	CV2809990	single nucleotide variant	NM_001145290.2(SLC37A2):c.690C>T (p.Ile230=)	not provided [RCV003424896]	likely benign	11	125080776	125080776	Human		name
597765571	CV3599845	single nucleotide variant	NM_001145290.2(SLC37A2):c.50G>C (p.Arg17Thr)	not specified [RCV004870438]	uncertain significance	11	125063417	125063417	Human		name
156278723	CV2284977	single nucleotide variant	NM_001145290.2(SLC37A2):c.130A>G (p.Ser44Gly)	not specified [RCV004143413]	uncertain significance	11	125076827	125076827	Human		name
156361598	CV2326636	single nucleotide variant	NM_001145290.2(SLC37A2):c.234T>G (p.Phe78Leu)	not specified [RCV004183171]	uncertain significance	11	125077322	125077322	Human		name
155984590	CV2344831	single nucleotide variant	NM_001145290.2(SLC37A2):c.136G>A (p.Val46Ile)	not specified [RCV004190973]	uncertain significance	11	125076833	125076833	Human		name
156067635	CV2345798	single nucleotide variant	NM_001145290.2(SLC37A2):c.100G>A (p.Ala34Thr)	not specified [RCV004205724]	likely benign	11	125076797	125076797	Human		name
156283286	CV2360563	single nucleotide variant	NM_001145290.2(SLC37A2):c.161G>T (p.Cys54Phe)	not specified [RCV004211322]	uncertain significance	11	125077249	125077249	Human		name
401910268	CV2809991	single nucleotide variant	NM_001145290.2(SLC37A2):c.1134G>C (p.Leu378=)	not provided [RCV003424897]	likely benign	11	125084833	125084833	Human		name
405785240	CV3332886	single nucleotide variant	NM_001145290.2(SLC37A2):c.146G>A (p.Arg49His)	not specified [RCV004459404]	uncertain significance	11	125077234	125077234	Human		name
405785246	CV3332887	single nucleotide variant	NM_001145290.2(SLC37A2):c.193C>T (p.His65Tyr)	not specified [RCV004459405]	uncertain significance	11	125077281	125077281	Human		name
405785251	CV3332888	single nucleotide variant	NM_001145290.2(SLC37A2):c.268G>A (p.Val90Met)	not specified [RCV004459406]	uncertain significance	11	125077482	125077482	Human		name
405785255	CV3332889	single nucleotide variant	NM_001145290.2(SLC37A2):c.290C>T (p.Ala97Val)	not specified [RCV004459407]	uncertain significance	11	125077504	125077504	Human		name
597702971	CV3599842	single nucleotide variant	NM_001145290.2(SLC37A2):c.101C>T (p.Ala34Val)	not specified [RCV004860148]	uncertain significance	11	125076798	125076798	Human		name
156170945	CV2197959	single nucleotide variant	NM_001145290.2(SLC37A2):c.637G>A (p.Val213Met)	not specified [RCV004077171]	uncertain significance	11	125080723	125080723	Human		name
156301538	CV2258507	single nucleotide variant	NM_001145290.2(SLC37A2):c.823T>G (p.Cys275Gly)	not specified [RCV004115999]	uncertain significance	11	125081844	125081844	Human		name
156087726	CV2337795	single nucleotide variant	NM_001145290.2(SLC37A2):c.691G>A (p.Glu231Lys)	not specified [RCV004183810]	uncertain significance	11	125080777	125080777	Human		name
401866652	CV2472799	single nucleotide variant	NM_001145290.2(SLC37A2):c.374G>C (p.Ser125Thr)	not provided [RCV003331496]	uncertain significance	11	125079171	125079171	Human		name
401727491	CV2678349	single nucleotide variant	NM_001145290.2(SLC37A2):c.629C>T (p.Ser210Leu)	not specified [RCV004292380]	uncertain significance	11	125080715	125080715	Human		name
401770444	CV2707214	single nucleotide variant	NM_001145290.2(SLC37A2):c.442G>A (p.Val148Ile)	not specified [RCV004310844]	uncertain significance	11	125079239	125079239	Human		name
401772231	CV2719577	single nucleotide variant	NM_001145290.2(SLC37A2):c.782C>T (p.Pro261Leu)	not specified [RCV004327253]	uncertain significance	11	125081803	125081803	Human		name
401867138	CV2759109	single nucleotide variant	NM_001145290.2(SLC37A2):c.309C>G (p.Phe103Leu)	not specified [RCV004342408]	uncertain significance	11	125077523	125077523	Human		name
401877624	CV2779887	single nucleotide variant	NM_001145290.2(SLC37A2):c.919G>A (p.Ala307Thr)	not specified [RCV004353502]	uncertain significance	11	125082277	125082277	Human		name
405785260	CV3332890	single nucleotide variant	NM_001145290.2(SLC37A2):c.343C>T (p.Arg115Cys)	not specified [RCV004459408]	uncertain significance	11	125079140	125079140	Human		name
405785270	CV3332892	single nucleotide variant	NM_001145290.2(SLC37A2):c.605G>T (p.Trp202Leu)	not specified [RCV004459410]	uncertain significance	11	125080691	125080691	Human		name
405785275	CV3332893	single nucleotide variant	NM_001145290.2(SLC37A2):c.634A>G (p.Ile212Val)	not specified [RCV004459411]	likely benign	11	125080720	125080720	Human		name
405785281	CV3332894	single nucleotide variant	NM_001145290.2(SLC37A2):c.718C>T (p.Pro240Ser)	not specified [RCV004459412]	uncertain significance	11	125081444	125081444	Human		name
405785284	CV3332895	single nucleotide variant	NM_001145290.2(SLC37A2):c.830A>G (p.Lys277Arg)	not specified [RCV004459413]	uncertain significance	11	125081851	125081851	Human		name
405785290	CV3332896	single nucleotide variant	NM_001145290.2(SLC37A2):c.907T>A (p.Cys303Ser)	not specified [RCV004459414]	uncertain significance	11	125082265	125082265	Human		name
407451601	CV3484525	single nucleotide variant	NM_001145290.2(SLC37A2):c.517G>A (p.Gly173Arg)	not specified [RCV004683714]	uncertain significance	11	125079750	125079750	Human		name
597702962	CV3599841	single nucleotide variant	NM_001145290.2(SLC37A2):c.476C>G (p.Thr159Arg)	not specified [RCV004860147]	uncertain significance	11	125079709	125079709	Human		name
597765564	CV3599843	single nucleotide variant	NM_001145290.2(SLC37A2):c.653C>T (p.Thr218Ile)	not specified [RCV004870436]	uncertain significance	11	125080739	125080739	Human		name
597765568	CV3599844	single nucleotide variant	NM_001145290.2(SLC37A2):c.633C>A (p.Phe211Leu)	not specified [RCV004870437]	uncertain significance	11	125080719	125080719	Human		name
597765574	CV3599846	single nucleotide variant	NM_001145290.2(SLC37A2):c.971A>G (p.Asn324Ser)	not specified [RCV004870439]	uncertain significance	11	125082329	125082329	Human		name
597765583	CV3599849	single nucleotide variant	NM_001145290.2(SLC37A2):c.889G>A (p.Val297Met)	not specified [RCV004870441]	uncertain significance	11	125082247	125082247	Human		name
598243323	CV3914898	single nucleotide variant	NM_001145290.2(SLC37A2):c.967G>A (p.Ala323Thr)	not specified [RCV005276688]	uncertain significance	11	125082325	125082325	Human		name
598243328	CV3914899	single nucleotide variant	NM_001145290.2(SLC37A2):c.340C>T (p.Leu114Phe)	not specified [RCV005276689]	uncertain significance	11	125079137	125079137	Human		name
598243332	CV3914900	single nucleotide variant	NM_001145290.2(SLC37A2):c.829A>G (p.Lys277Glu)	not specified [RCV005276690]	uncertain significance	11	125081850	125081850	Human		name
598243338	CV3914901	single nucleotide variant	NM_001145290.2(SLC37A2):c.745G>A (p.Glu249Lys)	not specified [RCV005276691]	uncertain significance	11	125081766	125081766	Human		name
598243343	CV3914902	single nucleotide variant	NM_001145290.2(SLC37A2):c.859A>C (p.Ser287Arg)	not specified [RCV005276692]	uncertain significance	11	125081880	125081880	Human		name
156065868	CV2240326	single nucleotide variant	NM_001145290.2(SLC37A2):c.1276G>A (p.Ala426Thr)	not specified [RCV004112880]	uncertain significance	11	125085422	125085422	Human		name
156284361	CV2288968	single nucleotide variant	NM_001145290.2(SLC37A2):c.1436G>A (p.Arg479Gln)	not specified [RCV004149927]	uncertain significance	11	125085964	125085964	Human		name
156078467	CV2375184	single nucleotide variant	NM_001145290.2(SLC37A2):c.1435C>T (p.Arg479Trp)	not specified [RCV004230224]	uncertain significance	11	125085963	125085963	Human		name
156033246	CV2376572	single nucleotide variant	NM_001145290.2(SLC37A2):c.1331C>T (p.Ala444Val)	not specified [RCV004220735]	uncertain significance	11	125085580	125085580	Human		name
401895674	CV2775046	single nucleotide variant	NM_001145290.2(SLC37A2):c.1411G>A (p.Val471Ile)	not specified [RCV004346425]	likely benign	11	125085660	125085660	Human		name
405785237	CV3332885	single nucleotide variant	NM_001145290.2(SLC37A2):c.1468G>T (p.Val490Leu)	not specified [RCV004459403]	uncertain significance	11	125085996	125085996	Human		name
407451604	CV3484528	single nucleotide variant	NM_001145290.2(SLC37A2):c.1319G>A (p.Gly440Asp)	not specified [RCV004683715]	uncertain significance	11	125085465	125085465	Human		name
407451607	CV3484529	single nucleotide variant	NM_001145290.2(SLC37A2):c.1259A>G (p.Lys420Arg)	not specified [RCV004683716]	uncertain significance	11	125085405	125085405	Human		name
407451610	CV3484530	single nucleotide variant	NM_001145290.2(SLC37A2):c.1393A>C (p.Met465Leu)	not specified [RCV004683717]	uncertain significance	11	125085642	125085642	Human		name
597702980	CV3599847	single nucleotide variant	NM_001145290.2(SLC37A2):c.1198C>G (p.Leu400Val)	not specified [RCV004860149]	uncertain significance	11	125085089	125085089	Human		name
597765578	CV3599848	single nucleotide variant	NM_001145290.2(SLC37A2):c.1110C>G (p.Ile370Met)	not specified [RCV004870440]	uncertain significance	11	125084304	125084304	Human		name
598243318	CV3914897	single nucleotide variant	NM_001145290.2(SLC37A2):c.1298C>T (p.Thr433Met)	not specified [RCV005276687]	uncertain significance	11	125085444	125085444	Human		name

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