Cenpi Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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45 records found for search term Cenpi

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
598129134	CV3888427	single nucleotide variant	NM_001386188.2(CENPI):c.687+8C>T	not provided [RCV005244601]	uncertain significance	X	101120792	101120792	Human		name
401921155	CV2826643	single nucleotide variant	NM_001386188.2(CENPI):c.1195+6A>G	not provided [RCV003432230]	uncertain significance	X	101128842	101128842	Human		name
401921152	CV2826641	single nucleotide variant	NM_001386188.2(CENPI):c.447C>T (p.Ser149=)	not provided [RCV003432228]	likely benign	X	101109555	101109555	Human		name
407461765	CV3418993	single nucleotide variant	NM_001386188.2(CENPI):c.59G>A (p.Ser20Asn)	not specified [RCV004612694]	uncertain significance	X	101101129	101101129	Human		name
598128625	CV3887830	single nucleotide variant	NM_001386188.2(CENPI):c.393G>A (p.Lys131=)	not provided [RCV005244004]	uncertain significance	X	101109501	101109501	Human		name
15135376	CV758199	single nucleotide variant	NM_001386188.2(CENPI):c.28G>A (p.Val10Ile)	not provided [RCV000920841]	benign	X	101101098	101101098	Human		name
401899893	CV2755859	single nucleotide variant	NM_001386188.2(CENPI):c.253G>T (p.Asp85Tyr)	not specified [RCV004342227]	uncertain significance	X	101102300	101102300	Human		name
401867280	CV2773197	single nucleotide variant	NM_001386188.2(CENPI):c.163G>C (p.Glu55Gln)	not specified [RCV004351920]	uncertain significance	X	101101233	101101233	Human		name
401921154	CV2826642	single nucleotide variant	NM_001386188.2(CENPI):c.1083T>C (p.Ser361=)	not provided [RCV003432229]	likely benign	X	101128724	101128724	Human		name
598227008	CV3894449	single nucleotide variant	NM_001386188.2(CENPI):c.1315C>T (p.Leu439=)	not provided [RCV005257692]	likely benign	X	101132217	101132217	Human		name
156240787	CV2213731	single nucleotide variant	NM_001386188.2(CENPI):c.402C>G (p.Ile134Met)	not specified [RCV004089803]	uncertain significance	X	101109510	101109510	Human		name
156232089	CV2227653	single nucleotide variant	NM_001386188.2(CENPI):c.584A>C (p.Asp195Ala)	not specified [RCV004094057]	uncertain significance	X	101109991	101109991	Human		name
156337314	CV2228672	single nucleotide variant	NM_001386188.2(CENPI):c.523A>C (p.Ile175Leu)	not specified [RCV004092892]	uncertain significance	X	101109930	101109930	Human		name
155993252	CV2281298	single nucleotide variant	NM_001386188.2(CENPI):c.938T>C (p.Leu313Pro)	not specified [RCV004147534]	uncertain significance	X	101127529	101127529	Human		name
156005017	CV2290271	single nucleotide variant	NM_001386188.2(CENPI):c.644A>G (p.Lys215Arg)	not specified [RCV004152918]	uncertain significance	X	101120741	101120741	Human		name
405761771	CV3300252	single nucleotide variant	NM_001386188.2(CENPI):c.344T>C (p.Ile115Thr)	not specified [RCV004433769]	uncertain significance	X	101102391	101102391	Human		name
407461768	CV3418994	single nucleotide variant	NM_001386188.2(CENPI):c.298T>C (p.Trp100Arg)	not specified [RCV004612695]	uncertain significance	X	101102345	101102345	Human		name
407461771	CV3418995	single nucleotide variant	NM_001386188.2(CENPI):c.848C>T (p.Pro283Leu)	not specified [RCV004612696]	uncertain significance	X	101127208	101127208	Human		name
597779485	CV3645494	single nucleotide variant	NM_001386188.2(CENPI):c.893G>A (p.Arg298His)	not specified [RCV004899279]	uncertain significance	X	101127253	101127253	Human		name
597779500	CV3645497	single nucleotide variant	NM_001386188.2(CENPI):c.440C>G (p.Ala147Gly)	not specified [RCV004899282]	uncertain significance	X	101109548	101109548	Human		name
597779503	CV3645498	single nucleotide variant	NM_001386188.2(CENPI):c.529C>T (p.Arg177Cys)	not specified [RCV004899283]	uncertain significance	X	101109936	101109936	Human		name
598208059	CV3951439	single nucleotide variant	NM_001386188.2(CENPI):c.397A>G (p.Met133Val)	not specified [RCV005315394]	uncertain significance	X	101109505	101109505	Human		name
598208078	CV3951445	single nucleotide variant	NM_001386188.2(CENPI):c.356G>A (p.Gly119Asp)	not specified [RCV005315398]	uncertain significance	X	101102403	101102403	Human		name
14399894	CV610474	single nucleotide variant	NM_001386188.2(CENPI):c.497G>A (p.Arg166His)	Premature ovarian insufficiency [RCV000766168]\|not provided [RCV003432762]	likely benign\|uncertain significance	X	101109904	101109904	Human	2	name
15191914	CV743052	single nucleotide variant	NM_001386188.2(CENPI):c.826G>A (p.Val276Met)	not provided [RCV000910386]	benign	X	101127186	101127186	Human		name
150409850	CV1196261	single nucleotide variant	NM_001386188.2(CENPI):c.2042A>G (p.Asn681Ser)	not provided [RCV001572819]	likely benign	X	101148109	101148109	Human		name
156074373	CV2248169	single nucleotide variant	NM_001386188.2(CENPI):c.2257A>G (p.Asn753Asp)	not specified [RCV004117565]	uncertain significance	X	101162953	101162953	Human		name
156199869	CV2293842	single nucleotide variant	NM_001386188.2(CENPI):c.2015G>C (p.Gly672Ala)	not specified [RCV004155105]	uncertain significance	X	101148082	101148082	Human		name
156390201	CV2373155	single nucleotide variant	NM_001386188.2(CENPI):c.1365C>A (p.Phe455Leu)	not specified [RCV004217840]	uncertain significance	X	101132267	101132267	Human		name
329396791	CV2455795	single nucleotide variant	NM_001386188.2(CENPI):c.1832G>A (p.Arg611His)	not specified [RCV004279086]	likely benign	X	101147768	101147768	Human		name
329378739	CV2459920	single nucleotide variant	NM_001386188.2(CENPI):c.1659C>A (p.Asn553Lys)	not specified [RCV004279411]	uncertain significance	X	101145157	101145157	Human		name
401754792	CV2682302	single nucleotide variant	NM_001386188.2(CENPI):c.2074G>A (p.Ala692Thr)	not specified [RCV004290344]	uncertain significance	X	101148141	101148141	Human		name
401884975	CV2771104	single nucleotide variant	NM_001386188.2(CENPI):c.1991A>G (p.Asp664Gly)	not specified [RCV004346108]	uncertain significance	X	101148058	101148058	Human		name
405761744	CV3300248	single nucleotide variant	NM_001386188.2(CENPI):c.1027C>A (p.Gln343Lys)	not specified [RCV004433765]	uncertain significance	X	101127618	101127618	Human		name
405761751	CV3300249	single nucleotide variant	NM_001386188.2(CENPI):c.1265T>G (p.Ile422Ser)	not specified [RCV004433766]	uncertain significance	X	101130051	101130051	Human		name
405761766	CV3300251	single nucleotide variant	NM_001386188.2(CENPI):c.1958C>T (p.Thr653Met)	not specified [RCV004433768]	uncertain significance	X	101148025	101148025	Human		name
407461761	CV3418992	single nucleotide variant	NM_001386188.2(CENPI):c.2170T>C (p.Phe724Leu)	not specified [RCV004612693]	uncertain significance	X	101162866	101162866	Human		name
407461847	CV3418996	single nucleotide variant	NM_001386188.2(CENPI):c.1941G>A (p.Met647Ile)	not specified [RCV004612697]	uncertain significance	X	101148008	101148008	Human		name
407461850	CV3418997	single nucleotide variant	NM_001386188.2(CENPI):c.1588A>G (p.Met530Val)	not specified [RCV004612698]	uncertain significance	X	101145086	101145086	Human		name
597779490	CV3645495	single nucleotide variant	NM_001386188.2(CENPI):c.1642A>C (p.Met548Leu)	not specified [RCV004899280]	uncertain significance	X	101145140	101145140	Human		name
597779495	CV3645496	single nucleotide variant	NM_001386188.2(CENPI):c.1021C>G (p.Leu341Val)	not specified [RCV004899281]	uncertain significance	X	101127612	101127612	Human		name
598241431	CV3951440	single nucleotide variant	NM_001386188.2(CENPI):c.2069G>A (p.Ser690Asn)	not specified [RCV005321545]	uncertain significance	X	101148136	101148136	Human		name
598241437	CV3951441	single nucleotide variant	NM_001386188.2(CENPI):c.1124A>G (p.Tyr375Cys)	not specified [RCV005321546]	uncertain significance	X	101128765	101128765	Human		name
598208065	CV3951442	single nucleotide variant	NM_001386188.2(CENPI):c.2021C>A (p.Ala674Asp)	not specified [RCV005315395]	uncertain significance	X	101148088	101148088	Human		name
598208071	CV3951443	single nucleotide variant	NM_001386188.2(CENPI):c.1867G>A (p.Val623Ile)	not specified [RCV005315396]	uncertain significance	X	101147803	101147803	Human		name

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