Cpne4 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 Cpne4

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8578012	CV112390	single nucleotide variant	NM_001289112.1(CPNE4):c.*2068C>T	Lung cancer [RCV000092913]	uncertain significance	3	131533127	131533127	Human		name
8578014	CV112392	single nucleotide variant	NM_001289112.1(CPNE4):c.235-2878G>T	Lung cancer [RCV000092915]	uncertain significance	3	131726503	131726503	Human		name
8578017	CV112395	single nucleotide variant	NM_001289112.1(CPNE4):c.53+13934C>A	Lung cancer [RCV000092918]	uncertain significance	3	132023623	132023623	Human		name
8578018	CV112396	single nucleotide variant	NM_001289112.1(CPNE4):c.53+13908C>A	Lung cancer [RCV000092919]	uncertain significance	3	132023649	132023649	Human		name
8578013	CV112391	single nucleotide variant	NM_001289112.1(CPNE4):c.736-13260G>A	Lung cancer [RCV000092914]	uncertain significance	3	131600842	131600842	Human		name
8578015	CV112393	single nucleotide variant	NM_001289112.1(CPNE4):c.234+88557T>G	Lung cancer [RCV000092916]	uncertain significance	3	131816707	131816707	Human		name
8578016	CV112394	single nucleotide variant	NM_001289112.1(CPNE4):c.234+47988C>T	Lung cancer [RCV000092917]	uncertain significance	3	131857276	131857276	Human		name
405696941	CV3245623	single nucleotide variant	NM_130808.3(CPNE4):c.5A>G (p.Lys2Arg)	not specified [RCV004374547]	uncertain significance	3	131905439	131905439	Human		name
407457171	CV3419659	single nucleotide variant	NM_130808.3(CPNE4):c.8A>T (p.Lys3Met)	not specified [RCV004611053]	uncertain significance	3	131905436	131905436	Human		name
405697128	CV3245619	single nucleotide variant	NM_130808.3(CPNE4):c.12G>A (p.Met4Ile)	not specified [RCV004374543]	uncertain significance	3	131905432	131905432	Human		name
156007896	CV2392668	single nucleotide variant	NM_130808.3(CPNE4):c.31G>A (p.Ala11Thr)	not specified [RCV004247049]	uncertain significance	3	131905413	131905413	Human		name
597651658	CV3651152	single nucleotide variant	NM_130808.3(CPNE4):c.71C>G (p.Thr24Ser)	not specified [RCV004910620]	uncertain significance	3	131905373	131905373	Human		name
597651679	CV3651154	single nucleotide variant	NM_130808.3(CPNE4):c.59G>A (p.Ser20Asn)	not specified [RCV004910622]	uncertain significance	3	131905385	131905385	Human		name
155950665	CV2302015	single nucleotide variant	NM_130808.3(CPNE4):c.275G>A (p.Arg92Gln)	not specified [RCV004158785]	uncertain significance	3	131723531	131723531	Human		name
405697116	CV3245621	single nucleotide variant	NM_130808.3(CPNE4):c.203G>A (p.Arg68His)	not specified [RCV004374545]	uncertain significance	3	131723603	131723603	Human		name
405696934	CV3245622	single nucleotide variant	NM_130808.3(CPNE4):c.269G>A (p.Arg90His)	not specified [RCV004374546]	uncertain significance	3	131723537	131723537	Human		name
597651688	CV3651155	single nucleotide variant	NM_130808.3(CPNE4):c.293T>G (p.Ile98Ser)	not specified [RCV004910623]	uncertain significance	3	131723513	131723513	Human		name
597651699	CV3651156	single nucleotide variant	NM_130808.3(CPNE4):c.238A>G (p.Thr80Ala)	not specified [RCV004910624]	uncertain significance	3	131723568	131723568	Human		name
597651706	CV3651157	single nucleotide variant	NM_130808.3(CPNE4):c.211A>G (p.Ile71Val)	not specified [RCV004910625]	uncertain significance	3	131723595	131723595	Human		name
598246591	CV3945290	single nucleotide variant	NM_130808.3(CPNE4):c.292A>G (p.Ile98Val)	not specified [RCV005322341]	uncertain significance	3	131723514	131723514	Human		name
8630600	CV85755	single nucleotide variant	NM_130808.2(CPNE4):c.1515C>T (p.Phe505=)	Malignant melanoma [RCV000065838]	not provided	3	131542581	131542581	Human		name
156234106	CV2223933	single nucleotide variant	NM_130808.3(CPNE4):c.305A>G (p.His102Arg)	not specified [RCV004094196]	uncertain significance	3	131723501	131723501	Human		name
155965793	CV2308553	single nucleotide variant	NM_130808.3(CPNE4):c.628T>C (p.Phe210Leu)	not specified [RCV004166829]	uncertain significance	3	131669728	131669728	Human		name
156205321	CV2311346	single nucleotide variant	NM_130808.3(CPNE4):c.325G>A (p.Asp109Asn)	not specified [RCV004166415]	uncertain significance	3	131723481	131723481	Human		name
155932187	CV2399974	single nucleotide variant	NM_130808.3(CPNE4):c.458A>G (p.Asn153Ser)	not specified [RCV004246903]	uncertain significance	3	131696591	131696591	Human		name
401890302	CV2768067	single nucleotide variant	NM_130808.3(CPNE4):c.485A>G (p.Asn162Ser)	not specified [RCV004348303]	uncertain significance	3	131696564	131696564	Human		name
597651667	CV3651153	single nucleotide variant	NM_130808.3(CPNE4):c.994C>G (p.Pro332Ala)	not specified [RCV004910621]	uncertain significance	3	131564283	131564283	Human		name
597651716	CV3651158	single nucleotide variant	NM_130808.3(CPNE4):c.640G>A (p.Val214Ile)	not specified [RCV004910626]	uncertain significance	3	131669716	131669716	Human		name
598246605	CV3945292	single nucleotide variant	NM_130808.3(CPNE4):c.772G>A (p.Gly258Arg)	not specified [RCV005322343]	uncertain significance	3	131587492	131587492	Human		name
598246611	CV3945293	single nucleotide variant	NM_130808.3(CPNE4):c.688G>C (p.Val230Leu)	not specified [RCV005322344]	uncertain significance	3	131587576	131587576	Human		name
8630601	CV85756	single nucleotide variant	NM_130808.2(CPNE4):c.884C>T (p.Ser295Phe)	Malignant melanoma [RCV000065839]	not provided	3	131575114	131575114	Human		name
156066280	CV2193307	single nucleotide variant	NM_130808.3(CPNE4):c.1565G>A (p.Ser522Asn)	not specified [RCV004071611]	uncertain significance	3	131535304	131535304	Human		name
156251716	CV2232331	single nucleotide variant	NM_130808.3(CPNE4):c.1670C>T (p.Pro557Leu)	not specified [RCV004098969]	uncertain significance	3	131535199	131535199	Human		name
155993702	CV2253610	single nucleotide variant	NM_130808.3(CPNE4):c.1408G>A (p.Val470Met)	not specified [RCV004125296]	uncertain significance	3	131542688	131542688	Human		name
156191295	CV2255237	single nucleotide variant	NM_130808.3(CPNE4):c.1610G>A (p.Gly537Asp)	not specified [RCV004117632]	uncertain significance	3	131535259	131535259	Human		name
401720231	CV2705770	single nucleotide variant	NM_130808.3(CPNE4):c.1258G>A (p.Val420Ile)	not specified [RCV004318606]	uncertain significance	3	131549991	131549991	Human		name
401899021	CV2785952	single nucleotide variant	NM_130808.3(CPNE4):c.1486G>C (p.Glu496Gln)	not specified [RCV004359796]	uncertain significance	3	131542610	131542610	Human		name
405697122	CV3245620	single nucleotide variant	NM_130808.3(CPNE4):c.1563G>C (p.Lys521Asn)	not specified [RCV004374544]	uncertain significance	3	131535306	131535306	Human		name
597651649	CV3651151	single nucleotide variant	NM_130808.3(CPNE4):c.1253A>G (p.Gln418Arg)	not specified [RCV004910619]	uncertain significance	3	131549996	131549996	Human		name
8625507	CV80630	single nucleotide variant	NM_130808.2(CPNE4):c.1454G>A (p.Gly485Asp)	Malignant melanoma [RCV000060707]	not provided	3	131542642	131542642	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