Cpne2 Variant Search Result - Rat Genome Database

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52 records found for search term Cpne2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401757622	CV2675421	single nucleotide variant	NM_152727.6(CPNE2):c.23G>T (p.Gly8Val)	not specified [RCV004292221]	uncertain significance	16	57110765	57110765	Human		name
155974313	CV2341418	single nucleotide variant	NM_152727.6(CPNE2):c.71G>A (p.Cys24Tyr)	not specified [RCV004188816]	uncertain significance	16	57110813	57110813	Human		name
155928771	CV2369560	single nucleotide variant	NM_152727.6(CPNE2):c.41C>A (p.Ala14Glu)	not specified [RCV004214979]	uncertain significance	16	57110783	57110783	Human		name
401752406	CV2682808	single nucleotide variant	NM_152727.6(CPNE2):c.35C>T (p.Ala12Val)	not specified [RCV004281779]	uncertain significance	16	57110777	57110777	Human		name
401733210	CV2713012	single nucleotide variant	NM_152727.6(CPNE2):c.65G>A (p.Cys22Tyr)	not specified [RCV004314715]	uncertain significance	16	57110807	57110807	Human		name
401866860	CV2769647	single nucleotide variant	NM_152727.6(CPNE2):c.47C>T (p.Pro16Leu)	not specified [RCV004351576]	uncertain significance	16	57110789	57110789	Human		name
156397950	CV2194009	single nucleotide variant	NM_152727.6(CPNE2):c.280G>A (p.Ala94Thr)	not specified [RCV004076775]	uncertain significance	16	57113387	57113387	Human		name
405697214	CV3245605	single nucleotide variant	NM_152727.6(CPNE2):c.119T>C (p.Val40Ala)	not specified [RCV004374529]	uncertain significance	16	57110861	57110861	Human		name
405697201	CV3245607	single nucleotide variant	NM_152727.6(CPNE2):c.184G>A (p.Asp62Asn)	not specified [RCV004374531]	uncertain significance	16	57113291	57113291	Human		name
407457151	CV3419651	single nucleotide variant	NM_152727.6(CPNE2):c.246C>G (p.Asp82Glu)	not specified [RCV004611045]	uncertain significance	16	57113353	57113353	Human		name
597651553	CV3651140	single nucleotide variant	NM_152727.6(CPNE2):c.202A>G (p.Ile68Val)	not specified [RCV004910608]	likely benign	16	57113309	57113309	Human		name
156278674	CV2210065	single nucleotide variant	NM_152727.6(CPNE2):c.439G>A (p.Ala147Thr)	not specified [RCV004076494]	uncertain significance	16	57117499	57117499	Human		name
155980948	CV2212097	single nucleotide variant	NM_152727.6(CPNE2):c.884C>T (p.Ser295Phe)	not specified [RCV004089005]	uncertain significance	16	57123430	57123430	Human		name
156059383	CV2239330	single nucleotide variant	NM_152727.6(CPNE2):c.575T>A (p.Leu192Gln)	not specified [RCV004114070]	uncertain significance	16	57119262	57119262	Human		name
156283231	CV2249739	single nucleotide variant	NM_152727.6(CPNE2):c.730G>A (p.Glu244Lys)	not specified [RCV004122509]	uncertain significance	16	57121141	57121141	Human		name
156355512	CV2324499	single nucleotide variant	NM_152727.6(CPNE2):c.766C>G (p.Arg256Gly)	not specified [RCV004178980]	uncertain significance	16	57121177	57121177	Human		name
156388340	CV2380317	single nucleotide variant	NM_152727.6(CPNE2):c.767G>A (p.Arg256Gln)	not specified [RCV004224664]	uncertain significance	16	57121178	57121178	Human		name
155908231	CV2387254	single nucleotide variant	NM_152727.6(CPNE2):c.698A>G (p.Tyr233Cys)	not specified [RCV004238349]	uncertain significance	16	57121109	57121109	Human		name
329376061	CV2437952	single nucleotide variant	NM_152727.6(CPNE2):c.466G>A (p.Val156Ile)	not specified [RCV004263671]	uncertain significance	16	57117526	57117526	Human		name
329372242	CV2443072	single nucleotide variant	NM_152727.6(CPNE2):c.967G>A (p.Asp323Asn)	not specified [RCV004253659]	uncertain significance	16	57125899	57125899	Human		name
401863799	CV2770835	single nucleotide variant	NM_152727.6(CPNE2):c.408C>G (p.Asp136Glu)	not specified [RCV004349867]	uncertain significance	16	57115523	57115523	Human		name
401873011	CV2776401	single nucleotide variant	NM_152727.6(CPNE2):c.461A>G (p.Asn154Ser)	not specified [RCV004355527]	uncertain significance	16	57117521	57117521	Human		name
401880881	CV2789414	single nucleotide variant	NM_152727.6(CPNE2):c.347G>A (p.Cys116Tyr)	not specified [RCV004360054]	uncertain significance	16	57113454	57113454	Human		name
405697193	CV3245608	single nucleotide variant	NM_152727.6(CPNE2):c.434C>T (p.Thr145Met)	not specified [RCV004374532]	uncertain significance	16	57115549	57115549	Human		name
405697187	CV3245609	single nucleotide variant	NM_152727.6(CPNE2):c.704A>G (p.Asn235Ser)	not specified [RCV004374533]	uncertain significance	16	57121115	57121115	Human		name
405697183	CV3245610	single nucleotide variant	NM_152727.6(CPNE2):c.779C>T (p.Pro260Leu)	not specified [RCV004374534]	uncertain significance	16	57121190	57121190	Human		name
405697177	CV3245611	single nucleotide variant	NM_152727.6(CPNE2):c.878A>C (p.Asp293Ala)	not specified [RCV004374535]	uncertain significance	16	57123424	57123424	Human		name
405697171	CV3245612	single nucleotide variant	NM_152727.6(CPNE2):c.962C>T (p.Pro321Leu)	not specified [RCV004374536]	uncertain significance	16	57125894	57125894	Human		name
405697163	CV3245613	single nucleotide variant	NM_152727.6(CPNE2):c.995C>G (p.Pro332Arg)	not specified [RCV004374537]	uncertain significance	16	57125927	57125927	Human		name
407457158	CV3419654	single nucleotide variant	NM_152727.6(CPNE2):c.568T>G (p.Trp190Gly)	not specified [RCV004611048]	uncertain significance	16	57119255	57119255	Human		name
597651507	CV3651135	single nucleotide variant	NM_152727.6(CPNE2):c.577G>A (p.Val193Ile)	not specified [RCV004910603]	uncertain significance	16	57119264	57119264	Human		name
597651536	CV3651138	single nucleotide variant	NM_152727.6(CPNE2):c.875G>A (p.Arg292Gln)	not specified [RCV004910606]	uncertain significance	16	57123421	57123421	Human		name
597651545	CV3651139	single nucleotide variant	NM_152727.6(CPNE2):c.457G>A (p.Asp153Asn)	not specified [RCV004910607]	uncertain significance	16	57117517	57117517	Human		name
597651578	CV3651143	single nucleotide variant	NM_152727.6(CPNE2):c.475C>A (p.Leu159Ile)	not specified [RCV004910611]	uncertain significance	16	57117535	57117535	Human		name
597651587	CV3651144	single nucleotide variant	NM_152727.6(CPNE2):c.658G>A (p.Gly220Arg)	not specified [RCV004910612]	uncertain significance	16	57119627	57119627	Human		name
597651596	CV3651145	single nucleotide variant	NM_152727.6(CPNE2):c.370A>G (p.Ser124Gly)	not specified [RCV004910613]	uncertain significance	16	57115485	57115485	Human		name
597651614	CV3651147	single nucleotide variant	NM_152727.6(CPNE2):c.319G>A (p.Glu107Lys)	not specified [RCV004910615]	uncertain significance	16	57113426	57113426	Human		name
598246517	CV3945279	single nucleotide variant	NM_152727.6(CPNE2):c.581A>G (p.His194Arg)	not specified [RCV005322330]	uncertain significance	16	57119268	57119268	Human		name
598246526	CV3945280	single nucleotide variant	NM_152727.6(CPNE2):c.494G>A (p.Arg165Lys)	not specified [RCV005322331]	likely benign	16	57117554	57117554	Human		name
598246540	CV3945282	single nucleotide variant	NM_152727.6(CPNE2):c.760G>A (p.Glu254Lys)	not specified [RCV005322333]	uncertain significance	16	57121171	57121171	Human		name
8627842	CV82986	single nucleotide variant	NM_152727.5(CPNE2):c.905G>A (p.Gly302Glu)	Malignant melanoma [RCV000063066]	not provided	16	57123451	57123451	Human		name
156301088	CV2322662	single nucleotide variant	NM_152727.6(CPNE2):c.1424C>T (p.Ala475Val)	not specified [RCV004182791]	uncertain significance	16	57146206	57146206	Human		name
156142738	CV2383794	single nucleotide variant	NM_152727.6(CPNE2):c.1249G>A (p.Val417Ile)	not specified [RCV004231666]	uncertain significance	16	57137229	57137229	Human		name
401869766	CV2772513	single nucleotide variant	NM_152727.6(CPNE2):c.1561A>G (p.Lys521Glu)	not specified [RCV004355285]	uncertain significance	16	57147572	57147572	Human		name
405697208	CV3245606	single nucleotide variant	NM_152727.6(CPNE2):c.1385A>G (p.Lys462Arg)	not specified [RCV004374530]	uncertain significance	16	57146167	57146167	Human		name
407457154	CV3419652	single nucleotide variant	NM_152727.6(CPNE2):c.1432G>A (p.Ala478Thr)	not specified [RCV004611046]	uncertain significance	16	57146214	57146214	Human		name
407457155	CV3419653	single nucleotide variant	NM_152727.6(CPNE2):c.1277A>G (p.Gln426Arg)	not specified [RCV004611047]	uncertain significance	16	57137257	57137257	Human		name
597651516	CV3651136	single nucleotide variant	NM_152727.6(CPNE2):c.1642G>A (p.Ala548Thr)	not specified [RCV004910604]	uncertain significance	16	57147653	57147653	Human		name
597651526	CV3651137	single nucleotide variant	NM_152727.6(CPNE2):c.1412G>A (p.Gly471Asp)	not specified [RCV004910605]	uncertain significance	16	57146194	57146194	Human		name
597651561	CV3651141	single nucleotide variant	NM_152727.6(CPNE2):c.1126G>A (p.Glu376Lys)	not specified [RCV004910609]	uncertain significance	16	57134784	57134784	Human		name
597651606	CV3651146	single nucleotide variant	NM_152727.6(CPNE2):c.1384A>C (p.Lys462Gln)	not specified [RCV004910614]	uncertain significance	16	57146166	57146166	Human		name
598246533	CV3945281	single nucleotide variant	NM_152727.6(CPNE2):c.1526G>A (p.Arg509Gln)	not specified [RCV005322332]	uncertain significance	16	57146308	57146308	Human		name

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