Xkrx Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)

40 records found for search term Xkrx

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401877950	CV2757715	single nucleotide variant	NM_212559.3(XKRX):c.26A>C (p.Glu9Ala)	not specified [RCV004336868]	uncertain significance	X	100928279	100928279	Human		name
401921148	CV2826638	single nucleotide variant	NM_212559.3(XKRX):c.288A>G (p.Lys96=)	not provided [RCV003432225]	likely benign	X	100928017	100928017	Human		name
597804633	CV3634238	single nucleotide variant	NM_212559.3(XKRX):c.22C>T (p.Pro8Ser)	not specified [RCV004882352]	uncertain significance	X	100928283	100928283	Human		name
329400683	CV2438653	single nucleotide variant	NM_212559.3(XKRX):c.64G>A (p.Asp22Asn)	not specified [RCV004261816]	uncertain significance	X	100928241	100928241	Human		name
401757750	CV2731425	single nucleotide variant	NM_212559.3(XKRX):c.89G>A (p.Arg30Gln)	not specified [RCV004330786]	uncertain significance	X	100928216	100928216	Human		name
401921147	CV2826637	single nucleotide variant	NM_212559.3(XKRX):c.765C>G (p.Leu255=)	not provided [RCV003432224]	likely benign	X	100914923	100914923	Human		name
597804631	CV3634234	single nucleotide variant	NM_212559.3(XKRX):c.56T>C (p.Leu19Pro)	not specified [RCV004882351]	uncertain significance	X	100928249	100928249	Human		name
597751464	CV3634236	single nucleotide variant	NM_212559.3(XKRX):c.70A>G (p.Ile24Val)	not specified [RCV004892783]	uncertain significance	X	100928235	100928235	Human		name
597804635	CV3634239	single nucleotide variant	NM_212559.3(XKRX):c.88C>G (p.Arg30Gly)	not specified [RCV004882353]	uncertain significance	X	100928217	100928217	Human		name
598183077	CV3933695	single nucleotide variant	NM_212559.3(XKRX):c.73C>T (p.Arg25Cys)	not specified [RCV005311343]	uncertain significance	X	100928232	100928232	Human		name
401921145	CV2826636	single nucleotide variant	NM_212559.3(XKRX):c.1107C>T (p.Phe369=)	not provided [RCV003432223]	likely benign	X	100914581	100914581	Human		name
405666465	CV3349550	single nucleotide variant	NM_212559.3(XKRX):c.171C>G (p.Ile57Met)	not specified [RCV004485577]	uncertain significance	X	100928134	100928134	Human		name
155956497	CV2281928	single nucleotide variant	NM_212559.3(XKRX):c.434G>A (p.Gly145Asp)	not specified [RCV004138702]	uncertain significance	X	100922963	100922963	Human		name
329374423	CV2443900	single nucleotide variant	NM_212559.3(XKRX):c.475C>T (p.Arg159Trp)	not specified [RCV004258232]	uncertain significance	X	100922922	100922922	Human		name
329389243	CV2448825	single nucleotide variant	NM_212559.3(XKRX):c.821T>C (p.Val274Ala)	not provided [RCV005256906]\|not specified [RCV004261512]	likely benign\|uncertain significance	X	100914867	100914867	Human		name
405666469	CV3349551	single nucleotide variant	NM_212559.3(XKRX):c.772C>G (p.Leu258Val)	not specified [RCV004485578]	uncertain significance	X	100914916	100914916	Human		name
405666474	CV3349552	single nucleotide variant	NM_212559.3(XKRX):c.908T>G (p.Phe303Cys)	not specified [RCV004485579]	uncertain significance	X	100914780	100914780	Human		name
407465626	CV3488226	single nucleotide variant	NM_212559.3(XKRX):c.919G>A (p.Gly307Ser)	not specified [RCV004688819]	uncertain significance	X	100914769	100914769	Human		name
597804625	CV3634231	single nucleotide variant	NM_212559.3(XKRX):c.848A>G (p.Glu283Gly)	not specified [RCV004882348]	uncertain significance	X	100914840	100914840	Human		name
597804628	CV3634232	single nucleotide variant	NM_212559.3(XKRX):c.874G>A (p.Gly292Ser)	not specified [RCV004882349]	uncertain significance	X	100914814	100914814	Human		name
597804629	CV3634233	single nucleotide variant	NM_212559.3(XKRX):c.616G>A (p.Val206Ile)	not specified [RCV004882350]	uncertain significance	X	100915072	100915072	Human		name
597751459	CV3634235	single nucleotide variant	NM_212559.3(XKRX):c.800T>C (p.Leu267Ser)	not specified [RCV004892782]	uncertain significance	X	100914888	100914888	Human		name
597751469	CV3634237	single nucleotide variant	NM_212559.3(XKRX):c.808G>A (p.Val270Met)	not specified [RCV004892784]	uncertain significance	X	100914880	100914880	Human		name
598275774	CV3933687	single nucleotide variant	NM_212559.3(XKRX):c.914G>A (p.Arg305Gln)	not specified [RCV005304908]	uncertain significance	X	100914774	100914774	Human		name
598183064	CV3933691	single nucleotide variant	NM_212559.3(XKRX):c.701G>T (p.Arg234Leu)	not specified [RCV005311341]	uncertain significance	X	100914987	100914987	Human		name
598183072	CV3933693	single nucleotide variant	NM_212559.3(XKRX):c.755C>A (p.Thr252Asn)	not specified [RCV005311342]	uncertain significance	X	100914933	100914933	Human		name
598275778	CV3933694	single nucleotide variant	NM_212559.3(XKRX):c.320T>C (p.Leu107Ser)	not specified [RCV005304912]	uncertain significance	X	100927985	100927985	Human		name
156069718	CV2203825	single nucleotide variant	NM_212559.3(XKRX):c.1237A>G (p.Thr413Ala)	not specified [RCV004074460]	likely benign	X	100914451	100914451	Human		name
156167951	CV2237275	single nucleotide variant	NM_212559.3(XKRX):c.1088T>C (p.Met363Thr)	not specified [RCV004115000]	uncertain significance	X	100914600	100914600	Human		name
156154519	CV2242314	single nucleotide variant	NM_212559.3(XKRX):c.1035C>A (p.Asn345Lys)	not specified [RCV004111329]	uncertain significance	X	100914653	100914653	Human		name
156032299	CV2259567	single nucleotide variant	NM_212559.3(XKRX):c.1345G>A (p.Val449Ile)	not specified [RCV004116616]	uncertain significance	X	100914343	100914343	Human		name
156256315	CV2325859	single nucleotide variant	NM_212559.3(XKRX):c.1106T>A (p.Phe369Tyr)	not specified [RCV004173731]	uncertain significance	X	100914582	100914582	Human		name
156344442	CV2364281	single nucleotide variant	NM_212559.3(XKRX):c.1094T>C (p.Leu365Ser)	not specified [RCV004223507]	uncertain significance	X	100914594	100914594	Human		name
405666454	CV3349548	single nucleotide variant	NM_212559.3(XKRX):c.1014T>G (p.Asp338Glu)	not specified [RCV004485575]	uncertain significance	X	100914674	100914674	Human		name
405666460	CV3349549	single nucleotide variant	NM_212559.3(XKRX):c.1291A>T (p.Thr431Ser)	not specified [RCV004485576]	uncertain significance	X	100914397	100914397	Human		name
407455962	CV3488225	single nucleotide variant	NM_212559.3(XKRX):c.1289G>A (p.Arg430Gln)	not specified [RCV004685765]	likely benign	X	100914399	100914399	Human		name
407455965	CV3488227	single nucleotide variant	NM_212559.3(XKRX):c.1156C>A (p.Gln386Lys)	not specified [RCV004685766]	uncertain significance	X	100914532	100914532	Human		name
598275775	CV3933689	single nucleotide variant	NM_212559.3(XKRX):c.1288C>T (p.Arg430Trp)	not specified [RCV005304909]	uncertain significance	X	100914400	100914400	Human		name
598275776	CV3933690	single nucleotide variant	NM_212559.3(XKRX):c.1187G>T (p.Gly396Val)	not specified [RCV005304910]	uncertain significance	X	100914501	100914501	Human		name
598275777	CV3933692	single nucleotide variant	NM_212559.3(XKRX):c.1111G>A (p.Gly371Arg)	not specified [RCV005304911]	uncertain significance	X	100914577	100914577	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