Ubxn7 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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23 records found for search term Ubxn7

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401942576	CV2839664	single nucleotide variant	NM_015562.2(UBXN7):c.74-1G>A	not provided [RCV003456597]	uncertain significance	3	196407394	196407394	Human		name
8578542	CV112926	single nucleotide variant	NM_015562.1(UBXN7):c.73+6162G>T	Lung cancer [RCV000093449]	uncertain significance	3	196426165	196426165	Human		name
329375748	CV2468797	single nucleotide variant	NM_015562.2(UBXN7):c.80G>C (p.Ser27Thr)	not specified [RCV004280113]	uncertain significance	3	196407387	196407387	Human		name
407523167	CV3491229	single nucleotide variant	NM_015562.2(UBXN7):c.35C>T (p.Ala12Val)	not specified [RCV004677950]	uncertain significance	3	196432365	196432365	Human		name
155971577	CV2309314	single nucleotide variant	NM_015562.2(UBXN7):c.220G>C (p.Glu74Gln)	not specified [RCV004165474]	uncertain significance	3	196407247	196407247	Human		name
156211907	CV2311658	single nucleotide variant	NM_015562.2(UBXN7):c.136G>A (p.Val46Ile)	not specified [RCV004168753]	uncertain significance	3	196407331	196407331	Human		name
401892079	CV2777214	single nucleotide variant	NM_015562.2(UBXN7):c.158G>A (p.Gly53Glu)	not specified [RCV004354247]	uncertain significance	3	196407309	196407309	Human		name
405800422	CV3337874	single nucleotide variant	NM_015562.2(UBXN7):c.223G>A (p.Glu75Lys)	not specified [RCV004477261]	uncertain significance	3	196403018	196403018	Human		name
597685215	CV3622777	single nucleotide variant	NM_015562.2(UBXN7):c.167C>G (p.Ala56Gly)	not specified [RCV004884023]	uncertain significance	3	196407300	196407300	Human		name
156119275	CV2219248	single nucleotide variant	NM_015562.2(UBXN7):c.994G>A (p.Val332Ile)	not specified [RCV004095129]	uncertain significance	3	196362528	196362528	Human		name
156070133	CV2325054	single nucleotide variant	NM_015562.2(UBXN7):c.584A>G (p.Asn195Ser)	not specified [RCV004175595]	uncertain significance	3	196371927	196371927	Human		name
329396289	CV2459487	single nucleotide variant	NM_015562.2(UBXN7):c.358C>T (p.Arg120Trp)	not specified [RCV004276953]	uncertain significance	3	196391923	196391923	Human		name
401721335	CV2673681	single nucleotide variant	NM_015562.2(UBXN7):c.952T>A (p.Ser318Thr)	not specified [RCV004282412]	uncertain significance	3	196362570	196362570	Human		name
407523170	CV3491230	single nucleotide variant	NM_015562.2(UBXN7):c.391A>G (p.Ile131Val)	not specified [RCV004677951]	uncertain significance	3	196391890	196391890	Human		name
597685233	CV3622779	single nucleotide variant	NM_015562.2(UBXN7):c.305G>A (p.Arg102Gln)	not specified [RCV004884025]	uncertain significance	3	196393604	196393604	Human		name
597685243	CV3622780	single nucleotide variant	NM_015562.2(UBXN7):c.479G>A (p.Cys160Tyr)	not specified [RCV004884026]	uncertain significance	3	196372032	196372032	Human		name
8630756	CV85911	single nucleotide variant	NM_015562.1(UBXN7):c.795T>G (p.Asp265Glu)	Malignant melanoma [RCV000065995]	not provided	3	196368067	196368067	Human		name
156363529	CV2265756	single nucleotide variant	NM_015562.2(UBXN7):c.1207G>C (p.Val403Leu)	not specified [RCV004124464]	uncertain significance	3	196362315	196362315	Human		name
405800420	CV3337873	single nucleotide variant	NM_015562.2(UBXN7):c.1214G>A (p.Gly405Glu)	not specified [RCV004477260]	uncertain significance	3	196362308	196362308	Human		name
407523475	CV3491231	single nucleotide variant	NM_015562.2(UBXN7):c.1216A>G (p.Ile406Val)	not specified [RCV004677952]	uncertain significance	3	196362306	196362306	Human		name
597685225	CV3622778	single nucleotide variant	NM_015562.2(UBXN7):c.1379G>A (p.Arg460Gln)	not specified [RCV004884024]	uncertain significance	3	196356776	196356776	Human		name
598265893	CV3929135	single nucleotide variant	NM_015562.2(UBXN7):c.1073G>A (p.Arg358Lys)	not specified [RCV005301817]	uncertain significance	3	196362449	196362449	Human		name
598265899	CV3929136	single nucleotide variant	NM_015562.2(UBXN7):c.1034C>T (p.Ala345Val)	not specified [RCV005301818]	uncertain significance	3	196362488	196362488	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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