Hpx Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

63 records found for search term Hpx

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15169222	CV724565	single nucleotide variant	NM_000613.3(HPX):c.24C>T (p.Pro8=)	not provided [RCV000883222]	benign	11	6440940	6440940	Human		name
405798555	CV3263625	single nucleotide variant	NM_000613.3(HPX):c.25G>A (p.Val9Ile)	not specified [RCV004402264]	likely benign	11	6440939	6440939	Human		name
15105504	CV713000	single nucleotide variant	NM_000613.3(HPX):c.19G>A (p.Ala7Thr)	not provided [RCV000959899]	benign	11	6440945	6440945	Human		name
329354647	CV2444612	single nucleotide variant	NM_000613.3(HPX):c.73C>T (p.Pro25Ser)	not specified [RCV004256833]	uncertain significance	11	6440891	6440891	Human		name
598192635	CV3971918	single nucleotide variant	NM_000613.3(HPX):c.35G>C (p.Gly12Ala)	not specified [RCV005354488]	uncertain significance	11	6440929	6440929	Human		name
15193430	CV724563	single nucleotide variant	NM_000613.3(HPX):c.534G>A (p.Lys178=)	not provided [RCV000888944]	benign	11	6437609	6437609	Human		name
156111143	CV2261708	single nucleotide variant	NM_000613.3(HPX):c.281C>T (p.Pro94Leu)	not specified [RCV004126012]	uncertain significance	11	6440220	6440220	Human		name
405798552	CV3263624	single nucleotide variant	NM_000613.3(HPX):c.145C>T (p.Arg49Cys)	not specified [RCV004402263]	uncertain significance	11	6440536	6440536	Human		name
597773321	CV3689484	single nucleotide variant	NM_000613.3(HPX):c.221T>G (p.Phe74Cys)	not specified [RCV004928857]	uncertain significance	11	6440280	6440280	Human		name
598205310	CV3971919	single nucleotide variant	NM_000613.3(HPX):c.239A>G (p.Lys80Arg)	not specified [RCV005337591]	uncertain significance	11	6440262	6440262	Human		name
15181985	CV712993	single nucleotide variant	NM_000613.3(HPX):c.1212C>T (p.Asp404=)	not provided [RCV000974524]	benign	11	6431388	6431388	Human		name
15180225	CV712994	single nucleotide variant	NM_000613.3(HPX):c.1176G>A (p.Thr392=)	not provided [RCV000974099]	benign	11	6431424	6431424	Human		name
15127644	CV712996	single nucleotide variant	NM_000613.3(HPX):c.1047C>T (p.Val349=)	not provided [RCV000963941]	benign	11	6431723	6431723	Human		name
15105496	CV712999	single nucleotide variant	NM_000613.3(HPX):c.118A>G (p.Thr40Ala)	not provided [RCV000959898]	benign	11	6440696	6440696	Human		name
15160067	CV724564	single nucleotide variant	NM_000613.3(HPX):c.247C>T (p.Arg83Trp)	not provided [RCV000881312]	benign	11	6440254	6440254	Human	16	name
15160067	CV724564	single nucleotide variant	NM_000613.3(HPX):c.247C>T (p.Arg83Trp)	not provided [RCV000881312]	benign	11	6440254	6440255	Human	16	name
156227496	CV2212773	single nucleotide variant	NM_000613.3(HPX):c.497G>A (p.Arg166His)	not specified [RCV004091465]	likely benign	11	6437646	6437646	Human		name
156135672	CV2213455	single nucleotide variant	NM_000613.3(HPX):c.496C>T (p.Arg166Cys)	not specified [RCV004087429]	uncertain significance	11	6437647	6437647	Human		name
156171565	CV2286721	single nucleotide variant	NM_000613.3(HPX):c.359C>G (p.Pro120Arg)	not specified [RCV004142544]	uncertain significance	11	6438487	6438487	Human		name
156087136	CV2341167	single nucleotide variant	NM_000613.3(HPX):c.589C>T (p.Arg197Cys)	not specified [RCV004181641]	uncertain significance	11	6437554	6437554	Human		name
156307050	CV2369589	single nucleotide variant	NM_000613.3(HPX):c.305G>A (p.Arg102His)	not specified [RCV004215002]	uncertain significance	11	6440196	6440196	Human		name
329378510	CV2447010	single nucleotide variant	NM_000613.3(HPX):c.812A>G (p.His271Arg)	not specified [RCV004257846]	uncertain significance	11	6437069	6437069	Human		name
401757519	CV2675351	single nucleotide variant	NM_000613.3(HPX):c.743C>G (p.Thr248Ser)	not specified [RCV004292159]	uncertain significance	11	6437138	6437138	Human		name
401864873	CV2791398	single nucleotide variant	NM_000613.3(HPX):c.618C>A (p.Phe206Leu)	not specified [RCV004358796]	uncertain significance	11	6437525	6437525	Human		name
405798558	CV3263626	single nucleotide variant	NM_000613.3(HPX):c.358C>T (p.Pro120Ser)	not specified [RCV004402265]	uncertain significance	11	6438488	6438488	Human		name
405798561	CV3263627	single nucleotide variant	NM_000613.3(HPX):c.493G>C (p.Asp165His)	not specified [RCV004402266]	uncertain significance	11	6437650	6437650	Human		name
405798564	CV3263628	single nucleotide variant	NM_000613.3(HPX):c.622C>T (p.Arg208Cys)	not specified [RCV004402267]	uncertain significance	11	6437521	6437521	Human		name
405798567	CV3263629	single nucleotide variant	NM_000613.3(HPX):c.644A>G (p.Glu215Gly)	not specified [RCV004402268]	uncertain significance	11	6437499	6437499	Human		name
405798570	CV3263630	single nucleotide variant	NM_000613.3(HPX):c.646G>A (p.Val216Met)	not specified [RCV004402269]	uncertain significance	11	6437497	6437497	Human		name
405798573	CV3263631	single nucleotide variant	NM_000613.3(HPX):c.664C>T (p.Arg222Trp)	not specified [RCV004402270]	uncertain significance	11	6437479	6437479	Human		name
405798576	CV3263632	single nucleotide variant	NM_000613.3(HPX):c.737A>G (p.Asn246Ser)	not specified [RCV004402271]	uncertain significance	11	6437144	6437144	Human		name
405798579	CV3263633	single nucleotide variant	NM_000613.3(HPX):c.812A>C (p.His271Pro)	not specified [RCV004402272]	uncertain significance	11	6437069	6437069	Human		name
407510820	CV3433911	single nucleotide variant	NM_000613.3(HPX):c.362C>A (p.Pro121His)	not specified [RCV004626257]	uncertain significance	11	6438484	6438484	Human		name
407528301	CV3433912	single nucleotide variant	NM_000613.3(HPX):c.566C>T (p.Ser189Phe)	not specified [RCV004633102]	uncertain significance	11	6437577	6437577	Human		name
597773282	CV3689475	single nucleotide variant	NM_000613.3(HPX):c.662C>T (p.Pro221Leu)	not specified [RCV004928849]	uncertain significance	11	6437481	6437481	Human		name
597773287	CV3689476	single nucleotide variant	NM_000613.3(HPX):c.721G>A (p.Gly241Arg)	not specified [RCV004928850]	likely benign	11	6437160	6437160	Human		name
597773292	CV3689477	single nucleotide variant	NM_000613.3(HPX):c.889A>G (p.Ile297Val)	not specified [RCV004928851]	uncertain significance	11	6431964	6431964	Human		name
597773297	CV3689478	single nucleotide variant	NM_000613.3(HPX):c.386C>T (p.Pro129Leu)	not specified [RCV004928852]	uncertain significance	11	6438460	6438460	Human		name
597773302	CV3689480	single nucleotide variant	NM_000613.3(HPX):c.974A>G (p.Gln325Arg)	not specified [RCV004928853]	uncertain significance	11	6431796	6431796	Human		name
597773307	CV3689481	single nucleotide variant	NM_000613.3(HPX):c.337G>A (p.Gly113Arg)	not specified [RCV004928854]	uncertain significance	11	6438509	6438509	Human		name
597773312	CV3689482	single nucleotide variant	NM_000613.3(HPX):c.598T>C (p.Cys200Arg)	not specified [RCV004928855]	uncertain significance	11	6437545	6437545	Human		name
598205303	CV3971916	single nucleotide variant	NM_000613.3(HPX):c.682T>C (p.Phe228Leu)	not specified [RCV005337590]	uncertain significance	11	6437461	6437461	Human		name
598192630	CV3971917	single nucleotide variant	NM_000613.3(HPX):c.628G>A (p.Asp210Asn)	not specified [RCV005354487]	likely benign	11	6437515	6437515	Human		name
598192642	CV3971920	single nucleotide variant	NM_000613.3(HPX):c.665G>A (p.Arg222Gln)	not specified [RCV005354489]	uncertain significance	11	6437478	6437478	Human		name
598192646	CV3971921	single nucleotide variant	NM_000613.3(HPX):c.393G>T (p.Leu131Phe)	not specified [RCV005354490]	uncertain significance	11	6438453	6438453	Human		name
598192651	CV3971922	single nucleotide variant	NM_000613.3(HPX):c.827C>T (p.Ala276Val)	not specified [RCV005354491]	uncertain significance	11	6437054	6437054	Human		name
15146605	CV712998	single nucleotide variant	NM_000613.3(HPX):c.521C>T (p.Thr174Met)	not provided [RCV000967189]	benign	11	6437622	6437622	Human		name
156232301	CV2273676	single nucleotide variant	NM_000613.3(HPX):c.1376G>T (p.Gly459Val)	not specified [RCV004132335]	uncertain significance	11	6431224	6431224	Human		name
156102902	CV2400167	single nucleotide variant	NM_000613.3(HPX):c.1263T>A (p.Asn421Lys)	not specified [RCV004242968]	uncertain significance	11	6431337	6431337	Human		name
329386323	CV2455854	single nucleotide variant	NM_000613.3(HPX):c.1123A>G (p.Met375Val)	not specified [RCV004279136]	uncertain significance	11	6431647	6431647	Human		name
329356886	CV2460601	single nucleotide variant	NM_000613.3(HPX):c.1163G>A (p.Gly388Glu)	not specified [RCV004268873]	uncertain significance	11	6431437	6431437	Human		name
405798534	CV3263618	single nucleotide variant	NM_000613.3(HPX):c.1018G>A (p.Gly340Ser)	not specified [RCV004402257]	uncertain significance	11	6431752	6431752	Human		name
405798537	CV3263619	single nucleotide variant	NM_000613.3(HPX):c.1051A>T (p.Thr351Ser)	not specified [RCV004402258]	likely benign	11	6431719	6431719	Human		name
405798540	CV3263620	single nucleotide variant	NM_000613.3(HPX):c.1135C>T (p.Arg379Trp)	not specified [RCV004402259]	uncertain significance	11	6431465	6431465	Human		name
405798543	CV3263621	single nucleotide variant	NM_000613.3(HPX):c.1241G>T (p.Gly414Val)	not specified [RCV004402260]	uncertain significance	11	6431359	6431359	Human		name
405798546	CV3263622	single nucleotide variant	NM_000613.3(HPX):c.1275G>T (p.Leu425Phe)	not specified [RCV004402261]	uncertain significance	11	6431325	6431325	Human		name
405798550	CV3263623	single nucleotide variant	NM_000613.3(HPX):c.1298T>C (p.Leu433Ser)	not specified [RCV004402262]	uncertain significance	11	6431302	6431302	Human		name
407528295	CV3433909	single nucleotide variant	NM_000613.3(HPX):c.1262A>G (p.Asn421Ser)	not specified [RCV004633100]	uncertain significance	11	6431338	6431338	Human		name
407528298	CV3433910	single nucleotide variant	NM_000613.3(HPX):c.1225A>G (p.Met409Val)	not specified [RCV004633101]	likely benign	11	6431375	6431375	Human		name
597773316	CV3689483	single nucleotide variant	NM_000613.3(HPX):c.1099C>T (p.Pro367Ser)	not specified [RCV004928856]	uncertain significance	11	6431671	6431671	Human		name
598192656	CV3971923	single nucleotide variant	NM_000613.3(HPX):c.1249T>C (p.Ser417Pro)	not specified [RCV005354492]	uncertain significance	11	6431351	6431351	Human		name
15138695	CV712995	single nucleotide variant	NM_000613.3(HPX):c.1111C>T (p.Arg371Trp)	not provided [RCV000965834]	benign	11	6431659	6431659	Human		name
15151138	CV752761	single nucleotide variant	NM_000613.3(HPX):c.1132C>T (p.Arg378Trp)	not provided [RCV000923612]	likely benign	11	6431468	6431468	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