Cpne8 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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29 records found for search term Cpne8

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8653943	CV130518	single nucleotide variant	NM_153634.2(CPNE8):c.331-3013C>T	Lung cancer [RCV000111005]	uncertain significance	12	38832468	38832468	Human		name
8653944	CV130519	single nucleotide variant	NM_153634.2(CPNE8):c.99-11013C>G	Lung cancer [RCV000111006]	uncertain significance	12	38885524	38885524	Human		name
401932027	CV2806855	deletion	NM_153634.3(CPNE8):c.187-9_187-6del	not provided [RCV003391707]	likely benign	12	38848668	38848671	Human		name
401776255	CV2706942	single nucleotide variant	NM_153634.3(CPNE8):c.11G>A (p.Arg4His)	not specified [RCV004321547]	uncertain significance	12	38905524	38905524	Human		name
597652277	CV3651199	single nucleotide variant	NM_153634.3(CPNE8):c.14A>G (p.Tyr5Cys)	not specified [RCV004910666]	uncertain significance	12	38905521	38905521	Human		name
405697281	CV3245658	single nucleotide variant	NM_153634.3(CPNE8):c.79G>A (p.Glu27Lys)	not specified [RCV004374582]	uncertain significance	12	38905456	38905456	Human		name
598246776	CV3945318	single nucleotide variant	NM_153634.3(CPNE8):c.65C>T (p.Pro22Leu)	not specified [RCV005322367]	uncertain significance	12	38905470	38905470	Human		name
401771622	CV2686265	single nucleotide variant	NM_153634.3(CPNE8):c.262G>A (p.Glu88Lys)	not specified [RCV004297350]	uncertain significance	12	38848587	38848587	Human		name
401773664	CV2695321	single nucleotide variant	NM_153634.3(CPNE8):c.161G>C (p.Gly54Ala)	not specified [RCV004303443]	uncertain significance	12	38873029	38873029	Human		name
597652315	CV3651203	single nucleotide variant	NM_153634.3(CPNE8):c.187T>C (p.Phe63Leu)	not specified [RCV004910670]	uncertain significance	12	38848662	38848662	Human		name
156027242	CV2278417	single nucleotide variant	NM_153634.3(CPNE8):c.995T>A (p.Met332Lys)	not specified [RCV004132872]	uncertain significance	12	38693805	38693805	Human		name
155916503	CV2282107	single nucleotide variant	NM_153634.3(CPNE8):c.614C>T (p.Thr205Ile)	not specified [RCV004138849]	uncertain significance	12	38762178	38762178	Human		name
155928656	CV2363337	single nucleotide variant	NM_153634.3(CPNE8):c.583A>G (p.Ile195Val)	not specified [RCV004213883]	uncertain significance	12	38762209	38762209	Human		name
401891821	CV2780820	single nucleotide variant	NM_153634.3(CPNE8):c.605T>A (p.Val202Asp)	not specified [RCV004352138]	uncertain significance	12	38762187	38762187	Human		name
407457272	CV3419676	single nucleotide variant	NM_153634.3(CPNE8):c.502A>G (p.Lys168Glu)	not specified [RCV004611070]	uncertain significance	12	38767708	38767708	Human		name
407457274	CV3419677	single nucleotide variant	NM_153634.3(CPNE8):c.940A>G (p.Ile314Val)	not specified [RCV004611071]	uncertain significance	12	38702896	38702896	Human		name
407457276	CV3419678	single nucleotide variant	NM_153634.3(CPNE8):c.554A>G (p.Tyr185Cys)	not specified [RCV004611072]	uncertain significance	12	38767656	38767656	Human		name
407457279	CV3419679	single nucleotide variant	NM_153634.3(CPNE8):c.311G>A (p.Ser104Asn)	not specified [RCV004611073]	uncertain significance	12	38839935	38839935	Human		name
407457282	CV3419680	single nucleotide variant	NM_153634.3(CPNE8):c.641A>G (p.Lys214Arg)	not specified [RCV004611074]	uncertain significance	12	38762151	38762151	Human		name
407457285	CV3419681	single nucleotide variant	NM_153634.3(CPNE8):c.587G>T (p.Cys196Phe)	not specified [RCV004611075]	uncertain significance	12	38762205	38762205	Human		name
597652260	CV3651197	single nucleotide variant	NM_153634.3(CPNE8):c.353G>T (p.Cys118Phe)	not specified [RCV004910664]	uncertain significance	12	38829433	38829433	Human		name
597652268	CV3651198	single nucleotide variant	NM_153634.3(CPNE8):c.626T>C (p.Val209Ala)	not specified [RCV004910665]	uncertain significance	12	38762166	38762166	Human		name
597652287	CV3651200	single nucleotide variant	NM_153634.3(CPNE8):c.748A>G (p.Thr250Ala)	not specified [RCV004910667]	uncertain significance	12	38730333	38730333	Human		name
597652297	CV3651201	single nucleotide variant	NM_153634.3(CPNE8):c.497C>T (p.Ala166Val)	not specified [RCV004910668]	uncertain significance	12	38767713	38767713	Human		name
597652308	CV3651202	single nucleotide variant	NM_153634.3(CPNE8):c.755A>G (p.Tyr252Cys)	not specified [RCV004910669]	uncertain significance	12	38730326	38730326	Human		name
597652323	CV3651204	single nucleotide variant	NM_153634.3(CPNE8):c.389G>A (p.Arg130His)	not specified [RCV004910671]	uncertain significance	12	38829397	38829397	Human		name
597652330	CV3651205	single nucleotide variant	NM_153634.3(CPNE8):c.401C>T (p.Pro134Leu)	not specified [RCV004910672]	uncertain significance	12	38829385	38829385	Human		name
598160073	CV3945317	single nucleotide variant	NM_153634.3(CPNE8):c.604G>A (p.Val202Ile)	not specified [RCV005328694]	uncertain significance	12	38762188	38762188	Human		name
329362118	CV2466021	single nucleotide variant	NM_153634.3(CPNE8):c.1437G>A (p.Met479Ile)	not specified [RCV004277920]	uncertain significance	12	38670798	38670798	Human		name

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