Slc7a10 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

78 records found for search term Slc7a10

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
150481408	CV1243305	single nucleotide variant	NM_019849.3(SLC7A10):c.*188C>T	not provided [RCV001652941]	benign	19	33208703	33208703	Human		name
150511594	CV1284733	duplication	NM_019849.3(SLC7A10):c.*132dup	not provided [RCV001721602]	benign	19	33208758	33208759	Human		name
150461794	CV1231521	single nucleotide variant	NM_019849.3(SLC7A10):c.913-11T>C	not provided [RCV001641088]	benign	19	33211339	33211339	Human		name
150430085	CV1231960	single nucleotide variant	NM_019849.3(SLC7A10):c.913-25T>C	not provided [RCV001641222]	benign	19	33211353	33211353	Human		name
150502646	CV1241612	single nucleotide variant	NM_019849.3(SLC7A10):c.508+51T>C	not provided [RCV001657203]	benign	19	33212800	33212800	Human		name
150509044	CV1244980	single nucleotide variant	NM_019849.3(SLC7A10):c.788+95G>A	not provided [RCV001659231]	benign	19	33212197	33212197	Human		name
150484263	CV1247100	single nucleotide variant	NM_019849.3(SLC7A10):c.635-21C>G	not provided [RCV001673596]	benign	19	33212466	33212466	Human		name
150451012	CV1232745	single nucleotide variant	NM_019849.3(SLC7A10):c.1264-54G>A	not provided [RCV001647820]	benign	19	33209539	33209539	Human		name
150470989	CV1269976	single nucleotide variant	NM_019849.3(SLC7A10):c.356+138G>C	not provided [RCV001695263]	benign	19	33215631	33215631	Human		name
150490546	CV1279797	single nucleotide variant	NM_019849.3(SLC7A10):c.1441+136G>A	not provided [RCV001716492]	benign	19	33209172	33209172	Human		name
401748189	CV2696550	single nucleotide variant	NM_019849.3(SLC7A10):c.43A>G (p.Arg15Gly)	not specified [RCV004312606]	likely benign	19	33225661	33225661	Human		name
401748193	CV2696551	single nucleotide variant	NM_019849.3(SLC7A10):c.45G>C (p.Arg15Ser)	not specified [RCV004312607]	likely benign	19	33225659	33225659	Human		name
401748195	CV2696552	single nucleotide variant	NM_019849.3(SLC7A10):c.68T>G (p.Val23Gly)	not specified [RCV004312608]	likely benign	19	33225636	33225636	Human		name
401748198	CV2696553	single nucleotide variant	NM_019849.3(SLC7A10):c.76A>C (p.Thr26Pro)	not specified [RCV004312609]	likely benign	19	33225628	33225628	Human		name
401748201	CV2696554	single nucleotide variant	NM_019849.3(SLC7A10):c.80T>G (p.Val27Gly)	not specified [RCV004312610]	likely benign	19	33225624	33225624	Human		name
407515619	CV3481072	single nucleotide variant	NM_019849.3(SLC7A10):c.59C>T (p.Pro20Leu)	not specified [RCV004674996]	uncertain significance	19	33225645	33225645	Human		name
597776571	CV3606708	single nucleotide variant	NM_019849.3(SLC7A10):c.29G>A (p.Gly10Glu)	not specified [RCV004872833]	likely benign	19	33225675	33225675	Human		name
15155055	CV741767	single nucleotide variant	NM_019849.3(SLC7A10):c.471C>T (p.Pro157=)	not provided [RCV000902070]	benign	19	33212888	33212888	Human		name
150500442	CV1213157	single nucleotide variant	NM_019849.3(SLC7A10):c.1374G>T (p.Thr458=)	not provided [RCV001594569]	benign	19	33209375	33209375	Human		name
150433200	CV1216831	single nucleotide variant	NM_019849.3(SLC7A10):c.1116C>T (p.Cys372=)	not provided [RCV001608733]	benign	19	33210614	33210614	Human		name
155918891	CV2333088	single nucleotide variant	NM_019849.3(SLC7A10):c.232G>A (p.Val78Ile)	not specified [RCV004194383]	uncertain significance	19	33215893	33215893	Human		name
155921891	CV2340530	single nucleotide variant	NM_019849.3(SLC7A10):c.172A>G (p.Ile58Val)	not specified [RCV004197247]	uncertain significance	19	33215953	33215953	Human		name
401885496	CV2759719	single nucleotide variant	NM_019849.3(SLC7A10):c.214G>A (p.Val72Met)	not specified [RCV004342771]	uncertain significance	19	33215911	33215911	Human		name
405731252	CV3322212	single nucleotide variant	NM_019849.3(SLC7A10):c.133G>A (p.Ala45Thr)	not specified [RCV004464364]	uncertain significance	19	33225571	33225571	Human		name
407515614	CV3481070	single nucleotide variant	NM_019849.3(SLC7A10):c.167C>T (p.Ser56Leu)	not specified [RCV004674994]	uncertain significance	19	33215958	33215958	Human		name
597776563	CV3606706	single nucleotide variant	NM_019849.3(SLC7A10):c.155A>C (p.Asn52Thr)	not specified [RCV004872831]	uncertain significance	19	33215970	33215970	Human		name
597776567	CV3606707	single nucleotide variant	NM_019849.3(SLC7A10):c.145A>G (p.Ile49Val)	not specified [RCV004872832]	uncertain significance	19	33225559	33225559	Human		name
156095928	CV2253079	single nucleotide variant	NM_019849.3(SLC7A10):c.390G>C (p.Met130Ile)	not specified [RCV004120865]	uncertain significance	19	33212969	33212969	Human		name
156244714	CV2267402	single nucleotide variant	NM_019849.3(SLC7A10):c.352G>A (p.Ala118Thr)	not specified [RCV004134052]	uncertain significance	19	33215773	33215773	Human		name
155929153	CV2363453	single nucleotide variant	NM_019849.3(SLC7A10):c.541C>T (p.Arg181Cys)	not specified [RCV004216028]	uncertain significance	19	33212607	33212607	Human		name
156166503	CV2373601	single nucleotide variant	NM_019849.3(SLC7A10):c.982G>A (p.Gly328Arg)	not specified [RCV004222694]	uncertain significance	19	33211259	33211259	Human		name
156149389	CV2377404	single nucleotide variant	NM_019849.3(SLC7A10):c.691G>A (p.Val231Met)	not specified [RCV004225581]	uncertain significance	19	33212389	33212389	Human		name
155907358	CV2389858	single nucleotide variant	NM_019849.3(SLC7A10):c.350T>C (p.Leu117Pro)	not specified [RCV004236075]	uncertain significance	19	33215775	33215775	Human		name
329385091	CV2454685	single nucleotide variant	NM_019849.3(SLC7A10):c.992A>G (p.Asn331Ser)	not specified [RCV004269925]	uncertain significance	19	33211249	33211249	Human		name
329374603	CV2464193	single nucleotide variant	NM_019849.3(SLC7A10):c.806T>C (p.Ile269Thr)	not specified [RCV004273872]	uncertain significance	19	33211520	33211520	Human		name
401742469	CV2673791	single nucleotide variant	NM_019849.3(SLC7A10):c.343G>A (p.Gly115Arg)	not specified [RCV004293176]	uncertain significance	19	33215782	33215782	Human		name
401773002	CV2709065	single nucleotide variant	NM_019849.3(SLC7A10):c.781G>C (p.Ala261Pro)	not specified [RCV004314405]	likely benign	19	33212299	33212299	Human		name
401884289	CV2789639	single nucleotide variant	NM_019849.3(SLC7A10):c.523G>A (p.Val175Met)	not specified [RCV004360239]	uncertain significance	19	33212625	33212625	Human		name
405731279	CV3322216	single nucleotide variant	NM_019849.3(SLC7A10):c.379G>A (p.Val127Ile)	not specified [RCV004464368]	uncertain significance	19	33212980	33212980	Human		name
405731286	CV3322217	single nucleotide variant	NM_019849.3(SLC7A10):c.496A>G (p.Met166Val)	not specified [RCV004464369]	uncertain significance	19	33212863	33212863	Human		name
405731298	CV3322218	single nucleotide variant	NM_019849.3(SLC7A10):c.610G>A (p.Val204Met)	not specified [RCV004464370]	likely benign	19	33212538	33212538	Human		name
405731304	CV3322219	single nucleotide variant	NM_019849.3(SLC7A10):c.643G>A (p.Glu215Lys)	not specified [RCV004464371]	uncertain significance	19	33212437	33212437	Human		name
405731311	CV3322220	single nucleotide variant	NM_019849.3(SLC7A10):c.659G>A (p.Ser220Asn)	not specified [RCV004464372]	uncertain significance	19	33212421	33212421	Human		name
405731317	CV3322221	single nucleotide variant	NM_019849.3(SLC7A10):c.835G>A (p.Val279Met)	not specified [RCV004464373]	uncertain significance	19	33211491	33211491	Human		name
407451934	CV3481073	single nucleotide variant	NM_019849.3(SLC7A10):c.868G>A (p.Ala290Thr)	not specified [RCV004683853]	uncertain significance	19	33211458	33211458	Human		name
407515622	CV3481074	single nucleotide variant	NM_019849.3(SLC7A10):c.298A>G (p.Ile100Val)	not specified [RCV004674997]	uncertain significance	19	33215827	33215827	Human		name
407515638	CV3481079	single nucleotide variant	NM_019849.3(SLC7A10):c.607G>A (p.Gly203Ser)	not specified [RCV004675002]	uncertain significance	19	33212541	33212541	Human		name
597724915	CV3606699	single nucleotide variant	NM_019849.3(SLC7A10):c.935G>T (p.Gly312Val)	not specified [RCV004862370]	uncertain significance	19	33211306	33211306	Human		name
597724944	CV3606702	single nucleotide variant	NM_019849.3(SLC7A10):c.722G>T (p.Gly241Val)	not specified [RCV004862373]	uncertain significance	19	33212358	33212358	Human		name
597776554	CV3606704	single nucleotide variant	NM_019849.3(SLC7A10):c.842C>T (p.Thr281Met)	not specified [RCV004872829]	uncertain significance	19	33211484	33211484	Human		name
598259960	CV3921988	single nucleotide variant	NM_019849.3(SLC7A10):c.685C>A (p.Pro229Thr)	not specified [RCV005279691]	uncertain significance	19	33212395	33212395	Human		name
150451387	CV1276588	single nucleotide variant	NM_019849.3(SLC7A10):c.1238G>A (p.Arg413Gln)	not provided [RCV001708377]	benign	19	33210492	33210492	Human		name
156226542	CV2203142	single nucleotide variant	NM_019849.3(SLC7A10):c.1132A>G (p.Ile378Val)	not specified [RCV004069380]	uncertain significance	19	33210598	33210598	Human		name
156239267	CV2221245	single nucleotide variant	NM_019849.3(SLC7A10):c.1357G>A (p.Val453Ile)	not specified [RCV004094682]	likely benign	19	33209392	33209392	Human		name
156207803	CV2250067	single nucleotide variant	NM_019849.3(SLC7A10):c.1412G>A (p.Ser471Asn)	not specified [RCV004116894]	uncertain significance	19	33209337	33209337	Human		name
156183610	CV2295676	single nucleotide variant	NM_019849.3(SLC7A10):c.1244C>T (p.Ala415Val)	not specified [RCV004149832]	uncertain significance	19	33210486	33210486	Human		name
156183577	CV2339352	single nucleotide variant	NM_019849.3(SLC7A10):c.1123A>G (p.Thr375Ala)	not specified [RCV004191581]	uncertain significance	19	33210607	33210607	Human		name
156256264	CV2359590	single nucleotide variant	NM_019849.3(SLC7A10):c.1507G>A (p.Glu503Lys)	not specified [RCV004214890]	uncertain significance	19	33208956	33208956	Human		name
329360932	CV2439900	single nucleotide variant	NM_019849.3(SLC7A10):c.1099G>A (p.Ala367Thr)	not specified [RCV004257937]	uncertain significance	19	33210816	33210816	Human		name
329392268	CV2441378	single nucleotide variant	NM_019849.3(SLC7A10):c.1397G>A (p.Gly466Glu)	not specified [RCV004257183]	uncertain significance	19	33209352	33209352	Human		name
329380102	CV2444193	single nucleotide variant	NM_019849.3(SLC7A10):c.1100C>T (p.Ala367Val)	not specified [RCV004260924]	uncertain significance	19	33210815	33210815	Human		name
401780428	CV2726070	single nucleotide variant	NM_019849.3(SLC7A10):c.1389C>G (p.Phe463Leu)	not specified [RCV004324425]	uncertain significance	19	33209360	33209360	Human		name
401867853	CV2767097	single nucleotide variant	NM_019849.3(SLC7A10):c.1454A>G (p.His485Arg)	not specified [RCV004347498]	likely benign	19	33209009	33209009	Human		name
401866637	CV2776293	single nucleotide variant	NM_019849.3(SLC7A10):c.1433G>A (p.Arg478Lys)	not specified [RCV004355446]	uncertain significance	19	33209316	33209316	Human		name
405731238	CV3322210	single nucleotide variant	NM_019849.3(SLC7A10):c.1042G>A (p.Gly348Arg)	not specified [RCV004464362]	uncertain significance	19	33210873	33210873	Human		name
405731246	CV3322211	single nucleotide variant	NM_019849.3(SLC7A10):c.1237C>T (p.Arg413Trp)	not specified [RCV004464363]	uncertain significance	19	33210493	33210493	Human		name
405731266	CV3322214	single nucleotide variant	NM_019849.3(SLC7A10):c.1447A>G (p.Met483Val)	not specified [RCV004464366]	uncertain significance	19	33209016	33209016	Human		name
405731272	CV3322215	single nucleotide variant	NM_019849.3(SLC7A10):c.1495G>T (p.Ala499Ser)	not specified [RCV004464367]	likely benign	19	33208968	33208968	Human		name
407515617	CV3481071	single nucleotide variant	NM_019849.3(SLC7A10):c.1229G>A (p.Arg410His)	not specified [RCV004674995]	uncertain significance	19	33210501	33210501	Human		name
407515625	CV3481075	single nucleotide variant	NM_019849.3(SLC7A10):c.1501G>C (p.Glu501Gln)	not specified [RCV004674998]	uncertain significance	19	33208962	33208962	Human		name
407515632	CV3481077	single nucleotide variant	NM_019849.3(SLC7A10):c.1024T>C (p.Phe342Leu)	not specified [RCV004675000]	uncertain significance	19	33210891	33210891	Human		name
407515635	CV3481078	single nucleotide variant	NM_019849.3(SLC7A10):c.1141G>A (p.Val381Met)	not specified [RCV004675001]	uncertain significance	19	33210589	33210589	Human		name
597724925	CV3606700	single nucleotide variant	NM_019849.3(SLC7A10):c.1564C>T (p.Pro522Ser)	not specified [RCV004862371]	uncertain significance	19	33208899	33208899	Human		name
597724934	CV3606701	single nucleotide variant	NM_019849.3(SLC7A10):c.1477G>A (p.Val493Met)	not specified [RCV004862372]	uncertain significance	19	33208986	33208986	Human		name
597776551	CV3606703	single nucleotide variant	NM_019849.3(SLC7A10):c.1201G>A (p.Val401Ile)	not specified [RCV004872828]	uncertain significance	19	33210529	33210529	Human		name
597776559	CV3606705	single nucleotide variant	NM_019849.3(SLC7A10):c.1501G>A (p.Glu501Lys)	not specified [RCV004872830]	uncertain significance	19	33208962	33208962	Human		name
598259955	CV3921987	single nucleotide variant	NM_019849.3(SLC7A10):c.1039G>A (p.Glu347Lys)	not specified [RCV005279690]	uncertain significance	19	33210876	33210876	Human		name
598259966	CV3921989	single nucleotide variant	NM_019849.3(SLC7A10):c.1543G>A (p.Ala515Thr)	not specified [RCV005279692]	uncertain significance	19	33208920	33208920	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