Dpep3 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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48 records found for search term Dpep3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155928497	CV2224389	single nucleotide variant	NM_001370198.1(DPEP3):c.-6C>T	not specified [RCV004097999]	uncertain significance	16	67980386	67980386	Human		name
597734422	CV3666973	single nucleotide variant	NM_001370198.1(DPEP3):c.-5G>T	not specified [RCV004920260]	uncertain significance	16	67980385	67980385	Human		name
156085557	CV2289841	single nucleotide variant	NM_001370198.1(DPEP3):c.-47C>G	not specified [RCV004150507]	uncertain significance	16	67980427	67980427	Human		name
598176538	CV3960759	single nucleotide variant	NM_001370198.1(DPEP3):c.-69C>G	not specified [RCV005332030]	likely benign	16	67980449	67980449	Human		name
401884016	CV2761224	single nucleotide variant	NM_001370198.1(DPEP3):c.88C>T (p.Arg30Trp)	not specified [RCV004341102]	uncertain significance	16	67980293	67980293	Human		name
597662959	CV3666964	single nucleotide variant	NM_001370198.1(DPEP3):c.70C>G (p.Leu24Val)	not specified [RCV004912119]	uncertain significance	16	67980311	67980311	Human		name
597662976	CV3666966	single nucleotide variant	NM_001370198.1(DPEP3):c.31G>A (p.Ala11Thr)	not specified [RCV004912121]	uncertain significance	16	67980350	67980350	Human		name
15098902	CV743609	single nucleotide variant	NM_001370198.1(DPEP3):c.363C>T (p.Ser121=)	not provided [RCV000906026]	benign	16	67979690	67979690	Human		name
156344871	CV2381959	single nucleotide variant	NM_001370198.1(DPEP3):c.101C>T (p.Thr34Ile)	not specified [RCV004225891]	uncertain significance	16	67980280	67980280	Human		name
401885501	CV2768209	single nucleotide variant	NM_001370198.1(DPEP3):c.292A>G (p.Asn98Asp)	not specified [RCV004350209]	uncertain significance	16	67979761	67979761	Human		name
405765913	CV3247801	single nucleotide variant	NM_001370198.1(DPEP3):c.293A>G (p.Asn98Ser)	not specified [RCV004384283]	uncertain significance	16	67979760	67979760	Human		name
597662985	CV3666967	single nucleotide variant	NM_001370198.1(DPEP3):c.281T>A (p.Val94Glu)	not specified [RCV004912122]	uncertain significance	16	67980100	67980100	Human		name
597663027	CV3666972	single nucleotide variant	NM_001370198.1(DPEP3):c.208A>G (p.Thr70Ala)	not specified [RCV004912127]	uncertain significance	16	67980173	67980173	Human		name
598176557	CV3960763	single nucleotide variant	NM_001370198.1(DPEP3):c.289C>T (p.His97Tyr)	not specified [RCV005332034]	uncertain significance	16	67979764	67979764	Human		name
156382147	CV2212605	single nucleotide variant	NM_001370198.1(DPEP3):c.327G>C (p.Lys109Asn)	not specified [RCV004085148]	uncertain significance	16	67979726	67979726	Human		name
155981386	CV2233073	single nucleotide variant	NM_001370198.1(DPEP3):c.815A>G (p.Asp272Gly)	not specified [RCV004103702]	uncertain significance	16	67977771	67977771	Human		name
156238808	CV2235849	single nucleotide variant	NM_001370198.1(DPEP3):c.851C>G (p.Ala284Gly)	not specified [RCV004111964]	uncertain significance	16	67977735	67977735	Human		name
156164117	CV2246748	single nucleotide variant	NM_001370198.1(DPEP3):c.950T>A (p.Ile317Asn)	not specified [RCV004112285]	uncertain significance	16	67977338	67977338	Human		name
156168128	CV2270538	single nucleotide variant	NM_001370198.1(DPEP3):c.751G>C (p.Gly251Arg)	not specified [RCV004137494]	uncertain significance	16	67977943	67977943	Human		name
155930446	CV2299912	single nucleotide variant	NM_001370198.1(DPEP3):c.939G>T (p.Lys313Asn)	not specified [RCV004149049]	uncertain significance	16	67977349	67977349	Human		name
156210094	CV2309619	single nucleotide variant	NM_001370198.1(DPEP3):c.685T>C (p.Trp229Arg)	not specified [RCV004158993]	uncertain significance	16	67978268	67978268	Human		name
156035476	CV2338914	single nucleotide variant	NM_001370198.1(DPEP3):c.952G>A (p.Val318Met)	not specified [RCV004184506]	uncertain significance	16	67977336	67977336	Human		name
156215904	CV2347924	single nucleotide variant	NM_001370198.1(DPEP3):c.992T>C (p.Leu331Pro)	not specified [RCV004197615]	uncertain significance	16	67977296	67977296	Human		name
156225619	CV2352670	single nucleotide variant	NM_001370198.1(DPEP3):c.496C>T (p.Arg166Cys)	not specified [RCV004198700]	uncertain significance	16	67978545	67978545	Human		name
329360881	CV2439852	single nucleotide variant	NM_001370198.1(DPEP3):c.736G>A (p.Gly246Arg)	not specified [RCV004257895]	uncertain significance	16	67977958	67977958	Human		name
401773749	CV2691394	single nucleotide variant	NM_001370198.1(DPEP3):c.712C>T (p.His238Tyr)	not specified [RCV004305256]	uncertain significance	16	67977982	67977982	Human		name
401857963	CV2774125	single nucleotide variant	NM_001370198.1(DPEP3):c.382G>C (p.Asp128His)	not specified [RCV004345718]	uncertain significance	16	67979671	67979671	Human		name
405765919	CV3247802	single nucleotide variant	NM_001370198.1(DPEP3):c.469G>C (p.Ala157Pro)	not specified [RCV004384284]	uncertain significance	16	67978572	67978572	Human		name
405765925	CV3247803	single nucleotide variant	NM_001370198.1(DPEP3):c.575T>C (p.Leu192Pro)	not specified [RCV004384285]	uncertain significance	16	67978378	67978378	Human		name
407506318	CV3434514	single nucleotide variant	NM_001370198.1(DPEP3):c.487C>T (p.Leu163Phe)	not specified [RCV004624663]	uncertain significance	16	67978554	67978554	Human		name
597734416	CV3666961	single nucleotide variant	NM_001370198.1(DPEP3):c.635A>T (p.Tyr212Phe)	not specified [RCV004920259]	uncertain significance	16	67978318	67978318	Human		name
597662942	CV3666962	single nucleotide variant	NM_001370198.1(DPEP3):c.439C>G (p.Gln147Glu)	not specified [RCV004912117]	uncertain significance	16	67978602	67978602	Human		name
597662952	CV3666963	single nucleotide variant	NM_001370198.1(DPEP3):c.626G>A (p.Arg209His)	not specified [RCV004912118]	uncertain significance	16	67978327	67978327	Human		name
597662968	CV3666965	single nucleotide variant	NM_001370198.1(DPEP3):c.577A>C (p.Ile193Leu)	not specified [RCV004912120]	uncertain significance	16	67978376	67978376	Human		name
597662995	CV3666968	single nucleotide variant	NM_001370198.1(DPEP3):c.340G>C (p.Asp114His)	not specified [RCV004912123]	uncertain significance	16	67979713	67979713	Human		name
597663003	CV3666969	single nucleotide variant	NM_001370198.1(DPEP3):c.787A>G (p.Met263Val)	not specified [RCV004912124]	uncertain significance	16	67977799	67977799	Human		name
597663011	CV3666970	single nucleotide variant	NM_001370198.1(DPEP3):c.976G>T (p.Val326Leu)	not specified [RCV004912125]	uncertain significance	16	67977312	67977312	Human		name
598176529	CV3960757	single nucleotide variant	NM_001370198.1(DPEP3):c.597C>G (p.His199Gln)	not specified [RCV005332028]	uncertain significance	16	67978356	67978356	Human		name
598176543	CV3960760	single nucleotide variant	NM_001370198.1(DPEP3):c.433T>A (p.Ser145Thr)	not specified [RCV005332031]	uncertain significance	16	67978608	67978608	Human		name
598176547	CV3960761	single nucleotide variant	NM_001370198.1(DPEP3):c.583G>A (p.Val195Met)	not specified [RCV005332032]	uncertain significance	16	67978370	67978370	Human		name
598176551	CV3960762	single nucleotide variant	NM_001370198.1(DPEP3):c.592G>C (p.Gly198Arg)	not specified [RCV005332033]	uncertain significance	16	67978361	67978361	Human		name
156223933	CV2229652	single nucleotide variant	NM_001370198.1(DPEP3):c.1271A>T (p.Glu424Val)	not specified [RCV004103465]	uncertain significance	16	67975961	67975961	Human		name
155998142	CV2287112	single nucleotide variant	NM_001370198.1(DPEP3):c.1182A>C (p.Gln394His)	not specified [RCV004144981]	uncertain significance	16	67976141	67976141	Human		name
156038150	CV2332605	single nucleotide variant	NM_001370198.1(DPEP3):c.1156C>T (p.Arg386Cys)	not specified [RCV004189287]	uncertain significance	16	67976167	67976167	Human		name
156304502	CV2341553	single nucleotide variant	NM_001370198.1(DPEP3):c.1373G>A (p.Arg458Gln)	not specified [RCV004188941]	likely benign	16	67975859	67975859	Human		name
401721013	CV2673569	single nucleotide variant	NM_001370198.1(DPEP3):c.1157G>A (p.Arg386His)	not specified [RCV004288532]	uncertain significance	16	67976166	67976166	Human		name
401745499	CV2681277	single nucleotide variant	NM_001370198.1(DPEP3):c.1370A>G (p.Asn457Ser)	not specified [RCV004289405]	likely benign	16	67975862	67975862	Human		name
401874228	CV2754666	single nucleotide variant	NM_001370198.1(DPEP3):c.1315G>A (p.Val439Met)	not specified [RCV004339338]	uncertain significance	16	67975917	67975917	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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