Slc17a3 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for All species
(View Results for all Objects and Ontologies)

44 records found for search term Slc17a3

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156103522	CV2352380	single nucleotide variant	NM_001098486.2(SLC17A3):c.49G>A (p.Ala17Thr)	not specified [RCV004200847]	uncertain significance	6	25868339	25868339	Human		name
401894588	CV2788098	single nucleotide variant	NM_001098486.2(SLC17A3):c.41G>A (p.Ser14Asn)	not specified [RCV004352727]	uncertain significance	6	25868347	25868347	Human		name
405711597	CV3328955	single nucleotide variant	NM_001098486.2(SLC17A3):c.41G>C (p.Ser14Thr)	not specified [RCV004448559]	uncertain significance	6	25868347	25868347	Human		name
405711614	CV3328957	single nucleotide variant	NM_001098486.2(SLC17A3):c.59T>C (p.Met20Thr)	not specified [RCV004448561]	uncertain significance	6	25868329	25868329	Human		name
598200013	CV3921695	single nucleotide variant	NM_001098486.2(SLC17A3):c.56A>T (p.Asp19Val)	not specified [RCV005268478]	uncertain significance	6	25868332	25868332	Human		name
156178408	CV2327415	single nucleotide variant	NM_001098486.2(SLC17A3):c.213C>A (p.Ser71Arg)	not specified [RCV004174838]	uncertain significance	6	25862323	25862323	Human		name
156072428	CV2328780	single nucleotide variant	NM_001098486.2(SLC17A3):c.124G>A (p.Ala42Thr)	not specified [RCV004178005]	uncertain significance	6	25862412	25862412	Human		name
156014405	CV2360114	single nucleotide variant	NM_001098486.2(SLC17A3):c.130G>A (p.Val44Ile)	not specified [RCV004215389]	likely benign	6	25862406	25862406	Human		name
155905894	CV2393819	single nucleotide variant	NM_001098486.2(SLC17A3):c.175A>G (p.Met59Val)	not specified [RCV004233648]	uncertain significance	6	25862361	25862361	Human		name
329376174	CV2438008	single nucleotide variant	NM_001098486.2(SLC17A3):c.155C>T (p.Thr52Met)	not specified [RCV004263717]	likely benign	6	25862381	25862381	Human		name
401869152	CV2766910	single nucleotide variant	NM_001098486.2(SLC17A3):c.137A>G (p.His46Arg)	not specified [RCV004343302]	uncertain significance	6	25862399	25862399	Human		name
401858156	CV2774219	single nucleotide variant	NM_001098486.2(SLC17A3):c.215C>T (p.Pro72Leu)	not specified [RCV004347594]	uncertain significance	6	25862321	25862321	Human		name
405258518	CV3203885	single nucleotide variant	NM_001098486.2(SLC17A3):c.1407C>T (p.Ala469=)	SLC17A3-related disorder [RCV003942047]	benign	6	25845472	25845472	Human		name , trait , alternate_id
405265758	CV3220829	single nucleotide variant	NM_001098486.2(SLC17A3):c.1140A>G (p.Ser380=)	SLC17A3-related disorder [RCV003969003]	benign	6	25849936	25849936	Human		name , trait , alternate_id
407503201	CV3477246	single nucleotide variant	NM_001098486.2(SLC17A3):c.188T>C (p.Met63Thr)	not specified [RCV004670174]	uncertain significance	6	25862348	25862348	Human		name
598268801	CV3921696	single nucleotide variant	NM_001098486.2(SLC17A3):c.241G>C (p.Glu81Gln)	not specified [RCV005281834]	uncertain significance	6	25862295	25862295	Human		name
8569878	CV45632	single nucleotide variant	NM_001098486.2(SLC17A3):c.202A>C (p.Asn68His)	Uric acid concentration, serum, quantitative trait locus 4 [RCV000030655]	risk factor	6	25862334	25862334	Human	1	name
155997409	CV2288623	single nucleotide variant	NM_001098486.2(SLC17A3):c.763G>A (p.Asp255Asn)	not specified [RCV004152137]	uncertain significance	6	25850827	25850827	Human		name
156006165	CV2299525	single nucleotide variant	NM_001098486.2(SLC17A3):c.832G>A (p.Val278Ile)	not specified [RCV004154868]	uncertain significance	6	25850620	25850620	Human		name
156068120	CV2320367	single nucleotide variant	NM_001098486.2(SLC17A3):c.626G>A (p.Gly209Glu)	not specified [RCV004178528]	uncertain significance	6	25855230	25855230	Human		name
405275235	CV3200017	single nucleotide variant	NM_001098486.2(SLC17A3):c.835G>A (p.Gly279Arg)	SLC17A3-related disorder [RCV003974023]	benign	6	25850617	25850617	Human		name , trait , alternate_id
405711588	CV3328954	single nucleotide variant	NM_001098486.2(SLC17A3):c.577T>G (p.Trp193Gly)	not specified [RCV004448558]	uncertain significance	6	25861672	25861672	Human		name
405711625	CV3328958	single nucleotide variant	NM_001098486.2(SLC17A3):c.853C>A (p.Leu285Ile)	not specified [RCV004448562]	uncertain significance	6	25850599	25850599	Human		name
597676210	CV3596267	single nucleotide variant	NM_001098486.2(SLC17A3):c.766C>T (p.Pro256Ser)	not specified [RCV004856944]	uncertain significance	6	25850824	25850824	Human		name
597676219	CV3596268	single nucleotide variant	NM_001098486.2(SLC17A3):c.952C>T (p.Pro318Ser)	not specified [RCV004856945]	uncertain significance	6	25850500	25850500	Human		name
597676228	CV3596269	single nucleotide variant	NM_001098486.2(SLC17A3):c.662G>A (p.Gly221Asp)	not specified [RCV004856946]	uncertain significance	6	25855194	25855194	Human		name
598245773	CV3896574	deletion	NM_001098486.2(SLC17A3):c.1006del (p.Ser336fs)	SLC17A3-related disorder [RCV005365847]	uncertain significance	6	25850165	25850165	Human		name , trait , alternate_id
598268797	CV3921694	single nucleotide variant	NM_001098486.2(SLC17A3):c.692C>A (p.Pro231His)	not specified [RCV005281833]	uncertain significance	6	25855164	25855164	Human		name
8569877	CV45631	single nucleotide variant	NM_001098486.2(SLC17A3):c.911T>C (p.Phe304Ser)	Uric acid concentration, serum, quantitative trait locus 4 [RCV000030654]	association	6	25850541	25850541	Human	1	name
155919249	CV2279386	single nucleotide variant	NM_001098486.2(SLC17A3):c.1223C>T (p.Thr408Ile)	not specified [RCV004141939]	uncertain significance	6	25849853	25849853	Human		name
156234504	CV2346286	single nucleotide variant	NM_001098486.2(SLC17A3):c.1229G>A (p.Cys410Tyr)	not specified [RCV004203774]	uncertain significance	6	25849847	25849847	Human		name
156105306	CV2361189	single nucleotide variant	NM_001098486.2(SLC17A3):c.1316T>C (p.Ile439Thr)	not specified [RCV004216372]	uncertain significance	6	25849420	25849420	Human		name
156017618	CV2370135	single nucleotide variant	NM_001098486.2(SLC17A3):c.1483C>T (p.Leu495Phe)	not specified [RCV004211020]	uncertain significance	6	25845396	25845396	Human		name
156286809	CV2370415	single nucleotide variant	NM_001098486.2(SLC17A3):c.1469C>T (p.Ala490Val)	not specified [RCV004215769]	uncertain significance	6	25845410	25845410	Human		name
156260205	CV2381107	single nucleotide variant	NM_001098486.2(SLC17A3):c.1490G>A (p.Arg497His)	not specified [RCV004225139]	uncertain significance	6	25845389	25845389	Human		name
156053225	CV2388520	single nucleotide variant	NM_001098486.2(SLC17A3):c.1274A>G (p.Tyr425Cys)	not specified [RCV004237372]	uncertain significance	6	25849462	25849462	Human		name
401893071	CV2758447	single nucleotide variant	NM_001098486.2(SLC17A3):c.1490G>T (p.Arg497Leu)	not specified [RCV004335099]	uncertain significance	6	25845389	25845389	Human		name
405284904	CV3190908	single nucleotide variant	NM_001098486.2(SLC17A3):c.1210T>A (p.Cys404Ser)	SLC17A3-related disorder [RCV003909471]	benign	6	25849866	25849866	Human		name , trait , alternate_id
405711574	CV3328952	single nucleotide variant	NM_001098486.2(SLC17A3):c.1319C>G (p.Ala440Gly)	not specified [RCV004448556]	uncertain significance	6	25849417	25849417	Human		name
405711581	CV3328953	single nucleotide variant	NM_001098486.2(SLC17A3):c.1381A>T (p.Arg461Trp)	not specified [RCV004448557]	uncertain significance	6	25845498	25845498	Human		name
407503198	CV3477245	single nucleotide variant	NM_001098486.2(SLC17A3):c.1489C>T (p.Arg497Cys)	not specified [RCV004670173]	uncertain significance	6	25845390	25845390	Human		name
597676239	CV3596270	single nucleotide variant	NM_001098486.2(SLC17A3):c.1100T>C (p.Val367Ala)	not specified [RCV004856947]	uncertain significance	6	25850071	25850071	Human		name
598268790	CV3921693	single nucleotide variant	NM_001098486.2(SLC17A3):c.1154C>T (p.Ser385Phe)	not specified [RCV005281832]	uncertain significance	6	25849922	25849922	Human		name
8631932	CV87138	single nucleotide variant	NM_001098486.1(SLC17A3):c.1124G>A (p.Gly375Glu)	Malignant melanoma [RCV000067229]	not provided	6	25849952	25849952	Human		name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Create Name:

Description:

Send us a Message