Nkrf Variant Search Result - Rat Genome Database

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39 records found for search term Nkrf

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401921625	CV2826883	single nucleotide variant	NM_001417890.1(NKRF):c.397-4A>G	not provided [RCV003432470]	likely benign	X	119591313	119591313	Human		name
401921494	CV2826887	single nucleotide variant	NM_001417890.1(NKRF):c.81G>C (p.Pro27=)	not provided [RCV003432474]	likely benign	X	119605916	119605916	Human		name
401921491	CV2826885	single nucleotide variant	NM_001417890.1(NKRF):c.222C>G (p.Leu74=)	not provided [RCV003432472]	likely benign	X	119605775	119605775	Human		name
401921493	CV2826886	single nucleotide variant	NM_001417890.1(NKRF):c.108A>T (p.Pro36=)	not provided [RCV003432473]	likely benign	X	119605889	119605889	Human		name
402516730	CV2936439	duplication	NM_001417890.1(NKRF):c.44dup (p.Pro16fs)	not provided [RCV003663005]	benign	X	119605952	119605953	Human		name
401921626	CV2826884	single nucleotide variant	NM_001417890.1(NKRF):c.375A>G (p.Lys125=)	not provided [RCV003432471]	likely benign	X	119592405	119592405	Human		name
15098937	CV758242	single nucleotide variant	NM_001417890.1(NKRF):c.459T>C (p.Pro153=)	not provided [RCV000912414]	benign	X	119591248	119591248	Human		name
15098852	CV729378	single nucleotide variant	NM_001417890.1(NKRF):c.2217T>C (p.Leu739=)	not provided [RCV000893987]	benign	X	119589490	119589490	Human		name
15098868	CV743121	single nucleotide variant	NM_001417890.1(NKRF):c.1257C>T (p.Ser419=)	not provided [RCV000896981]	benign	X	119590450	119590450	Human		name
155947314	CV2234799	single nucleotide variant	NM_001417890.1(NKRF):c.895C>T (p.Arg299Cys)	not specified [RCV004111235]	uncertain significance	X	119590812	119590812	Human		name
156364875	CV2272010	single nucleotide variant	NM_001417890.1(NKRF):c.884A>G (p.Tyr295Cys)	not specified [RCV004124816]	uncertain significance	X	119590823	119590823	Human		name
156346384	CV2305291	single nucleotide variant	NM_001417890.1(NKRF):c.443G>T (p.Arg148Ile)	not specified [RCV004171210]	uncertain significance	X	119591264	119591264	Human		name
156396265	CV2326184	single nucleotide variant	NM_001417890.1(NKRF):c.991A>G (p.Thr331Ala)	not specified [RCV004180452]	uncertain significance	X	119590716	119590716	Human		name
329354177	CV2447284	single nucleotide variant	NM_001417890.1(NKRF):c.505C>A (p.Pro169Thr)	not specified [RCV004262572]	uncertain significance	X	119591202	119591202	Human		name
329397190	CV2456675	single nucleotide variant	NM_001417890.1(NKRF):c.440C>T (p.Ala147Val)	not specified [RCV004277851]	likely benign	X	119591267	119591267	Human		name
405706668	CV3362234	single nucleotide variant	NM_001417890.1(NKRF):c.457C>A (p.Pro153Thr)	not specified [RCV004493222]	uncertain significance	X	119591250	119591250	Human		name
405706672	CV3362235	single nucleotide variant	NM_001417890.1(NKRF):c.484A>G (p.Lys162Glu)	not specified [RCV004493223]	uncertain significance	X	119591223	119591223	Human		name
405706689	CV3362237	single nucleotide variant	NM_001417890.1(NKRF):c.535G>A (p.Glu179Lys)	not specified [RCV004493225]	uncertain significance	X	119591172	119591172	Human		name
156233295	CV2273912	single nucleotide variant	NM_001417890.1(NKRF):c.1568C>T (p.Ser523Leu)	not specified [RCV004134320]	uncertain significance	X	119590139	119590139	Human		name
155985877	CV2282439	single nucleotide variant	NM_001417890.1(NKRF):c.1132C>T (p.Arg378Trp)	not specified [RCV004133247]	uncertain significance	X	119590575	119590575	Human		name
156012153	CV2358858	single nucleotide variant	NM_001417890.1(NKRF):c.1165C>G (p.Leu389Val)	not specified [RCV004212203]	uncertain significance	X	119590542	119590542	Human		name
155931466	CV2399849	single nucleotide variant	NM_001417890.1(NKRF):c.1537G>A (p.Val513Ile)	not specified [RCV004246794]	uncertain significance	X	119590170	119590170	Human		name
329381304	CV2440773	single nucleotide variant	NM_001417890.1(NKRF):c.1258G>A (p.Gly420Arg)	not specified [RCV004258716]	uncertain significance	X	119590449	119590449	Human		name
401720797	CV2702118	single nucleotide variant	NM_001417890.1(NKRF):c.1276G>A (p.Ala426Thr)	not specified [RCV004314478]	uncertain significance	X	119590431	119590431	Human		name
405706631	CV3362229	single nucleotide variant	NM_001417890.1(NKRF):c.1330A>G (p.Ile444Val)	not specified [RCV004493217]	uncertain significance	X	119590377	119590377	Human		name
405706638	CV3362230	single nucleotide variant	NM_001417890.1(NKRF):c.1708C>T (p.Leu570Phe)	not specified [RCV004493218]	uncertain significance	X	119589999	119589999	Human		name
405706645	CV3362231	single nucleotide variant	NM_001417890.1(NKRF):c.1709T>G (p.Leu570Arg)	not specified [RCV004493219]	uncertain significance	X	119589998	119589998	Human		name
405706652	CV3362232	single nucleotide variant	NM_001417890.1(NKRF):c.1924C>A (p.Gln642Lys)	not specified [RCV004493220]	uncertain significance	X	119589783	119589783	Human		name
405706660	CV3362233	single nucleotide variant	NM_001417890.1(NKRF):c.1936G>A (p.Asp646Asn)	not specified [RCV004493221]	uncertain significance	X	119589771	119589771	Human		name
407497452	CV3458612	single nucleotide variant	NM_001417890.1(NKRF):c.1521G>T (p.Gln507His)	not specified [RCV004643752]	uncertain significance	X	119590186	119590186	Human		name
407508830	CV3458613	single nucleotide variant	NM_001417890.1(NKRF):c.1244G>T (p.Gly415Val)	not specified [RCV004647243]	uncertain significance	X	119590463	119590463	Human		name
407508838	CV3458615	single nucleotide variant	NM_001417890.1(NKRF):c.2263G>A (p.Gly755Ser)	not specified [RCV004647245]	uncertain significance	X	119589444	119589444	Human		name
597650996	CV3556279	single nucleotide variant	NM_001417890.1(NKRF):c.2126G>A (p.Arg709His)	not specified [RCV004826837]	uncertain significance	X	119589581	119589581	Human		name
597651006	CV3556280	single nucleotide variant	NM_001417890.1(NKRF):c.1111C>T (p.Arg371Cys)	not specified [RCV004826838]	uncertain significance	X	119590596	119590596	Human		name
597651013	CV3556281	single nucleotide variant	NM_001417890.1(NKRF):c.1735G>C (p.Glu579Gln)	not specified [RCV004826839]	uncertain significance	X	119589972	119589972	Human		name
597651023	CV3556282	single nucleotide variant	NM_001417890.1(NKRF):c.1259G>T (p.Gly420Val)	not specified [RCV004826840]	uncertain significance	X	119590448	119590448	Human		name
597651030	CV3556283	single nucleotide variant	NM_001417890.1(NKRF):c.2302A>G (p.Lys768Glu)	not specified [RCV004826841]	uncertain significance	X	119589405	119589405	Human		name
598239156	CV3994610	single nucleotide variant	NM_001417890.1(NKRF):c.1699A>T (p.Met567Leu)	not specified [RCV005382872]	uncertain significance	X	119590008	119590008	Human		name
598193701	CV3994611	single nucleotide variant	NM_001417890.1(NKRF):c.2159G>C (p.Arg720Thr)	not specified [RCV005374592]	likely benign	X	119589548	119589548	Human		name

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