Xkr9 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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38 records found for search term Xkr9

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8650587	CV127162	single nucleotide variant	NM_001011720.1(XKR9):c.*99T>A	Lung cancer [RCV000107649]	uncertain significance	8	70734523	70734523	Human		name
598275773	CV3933686	single nucleotide variant	NM_001011720.2(XKR9):c.11C>G (p.Thr4Ser)	not specified [RCV005304907]	uncertain significance	8	70681069	70681069	Human		name
156248435	CV2221999	single nucleotide variant	NM_001011720.2(XKR9):c.260G>A (p.Gly87Glu)	not specified [RCV004102990]	uncertain significance	8	70681318	70681318	Human		name
156011399	CV2291140	single nucleotide variant	NM_001011720.2(XKR9):c.290A>G (p.Lys97Arg)	not specified [RCV004153450]	uncertain significance	8	70706950	70706950	Human		name
156063130	CV2352708	single nucleotide variant	NM_001011720.2(XKR9):c.204G>C (p.Lys68Asn)	not specified [RCV004198734]	uncertain significance	8	70681262	70681262	Human		name
405666406	CV3349538	single nucleotide variant	NM_001011720.2(XKR9):c.273G>T (p.Arg91Ser)	not specified [RCV004485565]	uncertain significance	8	70706933	70706933	Human		name
156380620	CV2208300	single nucleotide variant	NM_001011720.2(XKR9):c.479C>T (p.Ala160Val)	not specified [RCV004088739]	uncertain significance	8	70707139	70707139	Human		name
156077189	CV2230272	single nucleotide variant	NM_001011720.2(XKR9):c.314A>C (p.Lys105Thr)	not specified [RCV004099886]	likely benign	8	70706974	70706974	Human		name
156358089	CV2250868	single nucleotide variant	NM_001011720.2(XKR9):c.737C>T (p.Ala246Val)	not specified [RCV004123462]	uncertain significance	8	70734039	70734039	Human		name
156327393	CV2332099	single nucleotide variant	NM_001011720.2(XKR9):c.499G>A (p.Ala167Thr)	not specified [RCV004189141]	uncertain significance	8	70733801	70733801	Human		name
156253331	CV2366174	single nucleotide variant	NM_001011720.2(XKR9):c.358C>A (p.Leu120Ile)	not specified [RCV004210203]	uncertain significance	8	70707018	70707018	Human		name
155999639	CV2378608	single nucleotide variant	NM_001011720.2(XKR9):c.787T>C (p.Tyr263His)	not specified [RCV004231087]	uncertain significance	8	70734089	70734089	Human		name
329402099	CV2453976	single nucleotide variant	NM_001011720.2(XKR9):c.305C>A (p.Ala102Glu)	not specified [RCV004271643]	uncertain significance	8	70706965	70706965	Human		name
401780054	CV2676797	single nucleotide variant	NM_001011720.2(XKR9):c.908C>G (p.Thr303Ser)	not specified [RCV004290967]	uncertain significance	8	70734210	70734210	Human		name
401732846	CV2691127	single nucleotide variant	NM_001011720.2(XKR9):c.674T>A (p.Phe225Tyr)	not specified [RCV004301122]	uncertain significance	8	70733976	70733976	Human		name
401759885	CV2698662	single nucleotide variant	NM_001011720.2(XKR9):c.351A>C (p.Gln117His)	not specified [RCV004299130]	uncertain significance	8	70707011	70707011	Human		name
401770433	CV2715181	single nucleotide variant	NM_001011720.2(XKR9):c.535A>G (p.Thr179Ala)	not specified [RCV004324535]	uncertain significance	8	70733837	70733837	Human		name
401909237	CV2821131	single nucleotide variant	NM_001011720.2(XKR9):c.599G>A (p.Cys200Tyr)	not provided [RCV003423938]	likely benign	8	70733901	70733901	Human		name
405666410	CV3349539	single nucleotide variant	NM_001011720.2(XKR9):c.339C>A (p.Phe113Leu)	not specified [RCV004485566]	uncertain significance	8	70706999	70706999	Human		name
405666419	CV3349541	single nucleotide variant	NM_001011720.2(XKR9):c.431G>A (p.Cys144Tyr)	not specified [RCV004485568]	uncertain significance	8	70707091	70707091	Human		name
405666424	CV3349542	single nucleotide variant	NM_001011720.2(XKR9):c.458T>C (p.Ile153Thr)	not specified [RCV004485569]	uncertain significance	8	70707118	70707118	Human		name
405666429	CV3349543	single nucleotide variant	NM_001011720.2(XKR9):c.549A>C (p.Gln183His)	not specified [RCV004485570]	uncertain significance	8	70733851	70733851	Human		name
405666435	CV3349544	single nucleotide variant	NM_001011720.2(XKR9):c.604A>C (p.Lys202Gln)	not specified [RCV004485571]	uncertain significance	8	70733906	70733906	Human		name
405666437	CV3349545	single nucleotide variant	NM_001011720.2(XKR9):c.651G>A (p.Met217Ile)	not specified [RCV004485572]	uncertain significance	8	70733953	70733953	Human		name
405666442	CV3349546	single nucleotide variant	NM_001011720.2(XKR9):c.823T>G (p.Phe275Val)	not specified [RCV004485573]	uncertain significance	8	70734125	70734125	Human		name
405666448	CV3349547	single nucleotide variant	NM_001011720.2(XKR9):c.919G>A (p.Val307Ile)	not specified [RCV004485574]	uncertain significance	8	70734221	70734221	Human		name
407455952	CV3488221	single nucleotide variant	NM_001011720.2(XKR9):c.934A>G (p.Ile312Val)	not specified [RCV004685761]	uncertain significance	8	70734236	70734236	Human		name
407455957	CV3488223	single nucleotide variant	NM_001011720.2(XKR9):c.536C>G (p.Thr179Ser)	not specified [RCV004685763]	uncertain significance	8	70733838	70733838	Human		name
407455959	CV3488224	single nucleotide variant	NM_001011720.2(XKR9):c.488G>T (p.Ser163Ile)	not specified [RCV004685764]	uncertain significance	8	70707148	70707148	Human		name
597804617	CV3634227	single nucleotide variant	NM_001011720.2(XKR9):c.455A>G (p.Tyr152Cys)	not specified [RCV004882344]	uncertain significance	8	70707115	70707115	Human		name
597804621	CV3634229	single nucleotide variant	NM_001011720.2(XKR9):c.890G>A (p.Gly297Asp)	not specified [RCV004882346]	uncertain significance	8	70734192	70734192	Human		name
597804623	CV3634230	single nucleotide variant	NM_001011720.2(XKR9):c.856C>T (p.Pro286Ser)	not specified [RCV004882347]	uncertain significance	8	70734158	70734158	Human		name
598275771	CV3933684	single nucleotide variant	NM_001011720.2(XKR9):c.362A>C (p.His121Pro)	not specified [RCV005304905]	uncertain significance	8	70707022	70707022	Human		name
598275772	CV3933685	single nucleotide variant	NM_001011720.2(XKR9):c.704T>C (p.Leu235Ser)	not specified [RCV005304906]	uncertain significance	8	70734006	70734006	Human		name
15129695	CV711626	single nucleotide variant	NM_001011720.2(XKR9):c.547C>T (p.Gln183Ter)	not provided [RCV000964301]	benign	8	70733849	70733849	Human		name
8626607	CV81751	single nucleotide variant	NM_001011720.1(XKR9):c.816C>G (p.Ile272Met)	Malignant melanoma [RCV000061829]	not provided	8	70734118	70734118	Human		name
156274747	CV2293889	single nucleotide variant	NM_001011720.2(XKR9):c.1000C>T (p.Leu334Phe)	not specified [RCV004155145]	uncertain significance	8	70734302	70734302	Human		name
597804619	CV3634228	single nucleotide variant	NM_001011720.2(XKR9):c.1097G>A (p.Arg366Lys)	not specified [RCV004882345]	uncertain significance	8	70734399	70734399	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)

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

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