Kifc3 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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75 records found for search term Kifc3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156377568	CV2217053	single nucleotide variant	NM_001130100.2(KIFC3):c.20C>T (p.Thr7Met)	not specified [RCV004085736]	uncertain significance	16	57798224	57798224	Human		name
401768659	CV2685546	single nucleotide variant	NM_001130100.2(KIFC3):c.77C>G (p.Pro26Arg)	not specified [RCV004294561]	uncertain significance	16	57798167	57798167	Human		name
401750930	CV2700121	single nucleotide variant	NM_001130100.2(KIFC3):c.76C>G (p.Pro26Ala)	not specified [RCV004310523]	uncertain significance	16	57798168	57798168	Human		name
405807114	CV3269151	single nucleotide variant	NM_001130100.2(KIFC3):c.70C>T (p.Arg24Trp)	not specified [RCV004406388]	uncertain significance	16	57798174	57798174	Human		name
407469687	CV3452244	single nucleotide variant	NM_001130100.2(KIFC3):c.44C>T (p.Ser15Leu)	not specified [RCV004636956]	uncertain significance	16	57798200	57798200	Human		name
156060194	CV2239418	single nucleotide variant	NM_001130100.2(KIFC3):c.128C>T (p.Ala43Val)	not specified [RCV004114144]	uncertain significance	16	57798116	57798116	Human		name
155994632	CV2286437	single nucleotide variant	NM_001130100.2(KIFC3):c.232C>T (p.Arg78Cys)	not specified [RCV004139955]	uncertain significance	16	57795082	57795082	Human		name
156081329	CV2341385	single nucleotide variant	NM_001130100.2(KIFC3):c.116C>T (p.Pro39Leu)	not specified [RCV004188785]	uncertain significance	16	57798128	57798128	Human		name
156003468	CV2400885	single nucleotide variant	NM_001130100.2(KIFC3):c.265G>A (p.Val89Met)	not specified [RCV004244177]	uncertain significance	16	57795049	57795049	Human		name
401881616	CV2759486	single nucleotide variant	NM_001130100.2(KIFC3):c.281C>T (p.Pro94Leu)	not specified [RCV004338479]	uncertain significance	16	57795033	57795033	Human		name
597768363	CV3695372	single nucleotide variant	NM_001130100.2(KIFC3):c.176G>A (p.Arg59His)	not specified [RCV004927469]	uncertain significance	16	57795138	57795138	Human		name
598248955	CV3991151	single nucleotide variant	NM_001130100.2(KIFC3):c.130G>A (p.Ala44Thr)	not specified [RCV005366301]	uncertain significance	16	57798114	57798114	Human		name
15200813	CV703759	single nucleotide variant	NM_001130100.2(KIFC3):c.1578G>A (p.Ala526=)	not provided [RCV000957438]	benign	16	57764182	57764182	Human		name
156382831	CV2223656	single nucleotide variant	NM_001130100.2(KIFC3):c.496G>A (p.Gly166Ser)	not specified [RCV004093779]	uncertain significance	16	57771572	57771572	Human		name
156217345	CV2253855	single nucleotide variant	NM_001130100.2(KIFC3):c.406C>G (p.Arg136Gly)	not specified [RCV004127542]	uncertain significance	16	57771662	57771662	Human		name
156187772	CV2292488	single nucleotide variant	NM_001130100.2(KIFC3):c.902A>G (p.Gln301Arg)	not specified [RCV004150275]	uncertain significance	16	57770564	57770564	Human		name
156157365	CV2322564	single nucleotide variant	NM_001130100.2(KIFC3):c.661G>A (p.Asp221Asn)	not specified [RCV004182720]	uncertain significance	16	57771302	57771302	Human		name
155969036	CV2339378	single nucleotide variant	NM_001130100.2(KIFC3):c.406C>T (p.Arg136Trp)	not specified [RCV004191601]	uncertain significance	16	57771662	57771662	Human		name
156104075	CV2363520	single nucleotide variant	NM_001130100.2(KIFC3):c.860C>T (p.Ala287Val)	not specified [RCV004216091]	uncertain significance	16	57770606	57770606	Human		name
401740177	CV2684287	single nucleotide variant	NM_001130100.2(KIFC3):c.856G>A (p.Val286Met)	not specified [RCV004288943]	uncertain significance	16	57770610	57770610	Human		name
401721320	CV2709915	single nucleotide variant	NM_001130100.2(KIFC3):c.925C>T (p.Arg309Trp)	not specified [RCV004314992]	uncertain significance	16	57770541	57770541	Human		name
401750504	CV2715661	single nucleotide variant	NM_001130100.2(KIFC3):c.506C>G (p.Pro169Arg)	not specified [RCV004327037]	uncertain significance	16	57771562	57771562	Human		name
401780719	CV2727530	single nucleotide variant	NM_001130100.2(KIFC3):c.812C>A (p.Ala271Asp)	not specified [RCV004329723]	uncertain significance	16	57770654	57770654	Human		name
401875143	CV2791125	single nucleotide variant	NM_001130100.2(KIFC3):c.407G>A (p.Arg136Gln)	not specified [RCV004356494]	uncertain significance	16	57771661	57771661	Human		name
405807108	CV3269148	single nucleotide variant	NM_001130100.2(KIFC3):c.455G>A (p.Arg152His)	not specified [RCV004406385]	uncertain significance	16	57771613	57771613	Human		name
405807110	CV3269149	single nucleotide variant	NM_001130100.2(KIFC3):c.653G>A (p.Arg218Gln)	not specified [RCV004406386]	uncertain significance	16	57771310	57771310	Human		name
405807116	CV3269152	single nucleotide variant	NM_001130100.2(KIFC3):c.731T>C (p.Ile244Thr)	not specified [RCV004406389]	uncertain significance	16	57771232	57771232	Human		name
405807117	CV3269153	single nucleotide variant	NM_001130100.2(KIFC3):c.820G>A (p.Glu274Lys)	not specified [RCV004406390]	uncertain significance	16	57770646	57770646	Human		name
405807119	CV3269154	single nucleotide variant	NM_001130100.2(KIFC3):c.968G>A (p.Arg323Gln)	not specified [RCV004406391]	uncertain significance	16	57769927	57769927	Human		name
407469685	CV3452243	single nucleotide variant	NM_001130100.2(KIFC3):c.694C>T (p.Arg232Trp)	not specified [RCV004636955]	uncertain significance	16	57771269	57771269	Human		name
597638218	CV3695367	single nucleotide variant	NM_001130100.2(KIFC3):c.967C>T (p.Arg323Trp)	not specified [RCV004941119]	uncertain significance	16	57769928	57769928	Human		name
597638223	CV3695369	single nucleotide variant	NM_001130100.2(KIFC3):c.529A>C (p.Ser177Arg)	not specified [RCV004941120]	uncertain significance	16	57771434	57771434	Human		name
597638228	CV3695370	single nucleotide variant	NM_001130100.2(KIFC3):c.832C>T (p.Arg278Trp)	not specified [RCV004941121]	uncertain significance	16	57770634	57770634	Human		name
597638234	CV3695371	single nucleotide variant	NM_001130100.2(KIFC3):c.451C>T (p.Arg151Trp)	not specified [RCV004941122]	uncertain significance	16	57771617	57771617	Human		name
597638240	CV3695373	single nucleotide variant	NM_001130100.2(KIFC3):c.932G>A (p.Arg311Gln)	not specified [RCV004941123]	uncertain significance	16	57770534	57770534	Human		name
597638249	CV3695375	single nucleotide variant	NM_001130100.2(KIFC3):c.833G>A (p.Arg278Gln)	not specified [RCV004941125]	uncertain significance	16	57770633	57770633	Human		name
597638254	CV3695377	single nucleotide variant	NM_001130100.2(KIFC3):c.402G>C (p.Lys134Asn)	not specified [RCV004941126]	uncertain significance	16	57771666	57771666	Human		name
597638259	CV3695378	single nucleotide variant	NM_001130100.2(KIFC3):c.931C>T (p.Arg311Trp)	not specified [RCV004941127]	uncertain significance	16	57770535	57770535	Human		name
156161136	CV2236423	single nucleotide variant	NM_001130100.2(KIFC3):c.1277G>C (p.Arg426Pro)	not specified [RCV004108098]	uncertain significance	16	57766927	57766927	Human		name
156055138	CV2243158	single nucleotide variant	NM_001130100.2(KIFC3):c.1837G>C (p.Glu613Gln)	not specified [RCV004110059]	uncertain significance	16	57761448	57761448	Human		name
156166723	CV2243632	single nucleotide variant	NM_001130100.2(KIFC3):c.1577C>A (p.Ala526Glu)	not specified [RCV004114349]	uncertain significance	16	57764183	57764183	Human		name
156138830	CV2280703	single nucleotide variant	NM_001130100.2(KIFC3):c.1400A>G (p.Asn467Ser)	not specified [RCV004143162]	uncertain significance	16	57765571	57765571	Human		name
155986048	CV2282485	single nucleotide variant	NM_001130100.2(KIFC3):c.2450C>A (p.Ser817Tyr)	not specified [RCV004133280]	uncertain significance	16	57759754	57759754	Human		name
156092933	CV2300179	single nucleotide variant	NM_001130100.2(KIFC3):c.2126C>G (p.Ala709Gly)	not specified [RCV004151368]	uncertain significance	16	57760832	57760832	Human		name
156071109	CV2328473	single nucleotide variant	NM_001130100.2(KIFC3):c.1022G>C (p.Arg341Pro)	not specified [RCV004175854]	uncertain significance	16	57769873	57769873	Human		name
156304929	CV2338589	single nucleotide variant	NM_001130100.2(KIFC3):c.2456G>A (p.Arg819Gln)	not specified [RCV004182180]	uncertain significance	16	57759748	57759748	Human		name
155984830	CV2368006	single nucleotide variant	NM_001130100.2(KIFC3):c.1961C>T (p.Thr654Met)	not specified [RCV004223093]	uncertain significance	16	57761083	57761083	Human		name
156178443	CV2374597	single nucleotide variant	NM_001130100.2(KIFC3):c.2440C>T (p.Arg814Cys)	not specified [RCV004225222]	uncertain significance	16	57759764	57759764	Human		name
156086090	CV2390777	single nucleotide variant	NM_001130100.2(KIFC3):c.2387C>T (p.Thr796Met)	not specified [RCV004241063]	uncertain significance	16	57759817	57759817	Human		name
329387027	CV2436216	single nucleotide variant	NM_001130100.2(KIFC3):c.2000C>T (p.Thr667Met)	not specified [RCV004249845]	uncertain significance	16	57761044	57761044	Human		name
401757561	CV2675377	single nucleotide variant	NM_001130100.2(KIFC3):c.1372G>A (p.Glu458Lys)	not specified [RCV004292184]	uncertain significance	16	57765599	57765599	Human		name
401741348	CV2680602	single nucleotide variant	NM_001130100.2(KIFC3):c.1994G>A (p.Arg665His)	not specified [RCV004291225]	uncertain significance	16	57761050	57761050	Human		name
401736435	CV2688789	single nucleotide variant	NM_001130100.2(KIFC3):c.1169G>A (p.Arg390His)	not specified [RCV004303812]	uncertain significance	16	57769644	57769644	Human		name
401742565	CV2697808	single nucleotide variant	NM_001130100.2(KIFC3):c.1502C>T (p.Ser501Leu)	not specified [RCV004300528]	uncertain significance	16	57765469	57765469	Human		name
401772791	CV2719760	single nucleotide variant	NM_001130100.2(KIFC3):c.2324G>A (p.Arg775His)	not specified [RCV004329194]	uncertain significance	16	57760325	57760325	Human		name
401739139	CV2722063	single nucleotide variant	NM_001130100.2(KIFC3):c.1157A>G (p.Lys386Arg)	not specified [RCV004326542]	uncertain significance	16	57769656	57769656	Human		name
401874650	CV2759304	single nucleotide variant	NM_001130100.2(KIFC3):c.1420G>A (p.Asp474Asn)	not specified [RCV004335891]	uncertain significance	16	57765551	57765551	Human		name
401877768	CV2761533	single nucleotide variant	NM_001130100.2(KIFC3):c.1234G>A (p.Glu412Lys)	not specified [RCV004334703]	uncertain significance	16	57766970	57766970	Human		name
401898006	CV2770054	single nucleotide variant	NM_001130100.2(KIFC3):c.1906G>A (p.Glu636Lys)	not specified [RCV004353871]	uncertain significance	16	57761138	57761138	Human		name
401858862	CV2774957	single nucleotide variant	NM_001130100.2(KIFC3):c.1216G>A (p.Glu406Lys)	not specified [RCV004346359]	uncertain significance	16	57769597	57769597	Human		name
401880926	CV2787719	single nucleotide variant	NM_001130100.2(KIFC3):c.1714G>A (p.Val572Ile)	not specified [RCV004356636]	uncertain significance	16	57762174	57762174	Human		name
405807091	CV3269140	single nucleotide variant	NM_001130100.2(KIFC3):c.1085C>A (p.Ala362Glu)	not specified [RCV004406377]	uncertain significance	16	57769810	57769810	Human		name
405807096	CV3269142	single nucleotide variant	NM_001130100.2(KIFC3):c.1288C>A (p.Gln430Lys)	not specified [RCV004406379]	uncertain significance	16	57766916	57766916	Human		name
405807098	CV3269143	single nucleotide variant	NM_001130100.2(KIFC3):c.1297A>G (p.Lys433Glu)	not specified [RCV004406380]	uncertain significance	16	57766907	57766907	Human		name
405807100	CV3269144	single nucleotide variant	NM_001130100.2(KIFC3):c.1421A>C (p.Asp474Ala)	not specified [RCV004406381]	uncertain significance	16	57765550	57765550	Human		name
405807102	CV3269145	single nucleotide variant	NM_001130100.2(KIFC3):c.1594G>A (p.Ala532Thr)	not specified [RCV004406382]	uncertain significance	16	57764166	57764166	Human		name
405807104	CV3269146	single nucleotide variant	NM_001130100.2(KIFC3):c.2084A>G (p.Gln695Arg)	not specified [RCV004406383]	uncertain significance	16	57760874	57760874	Human		name
407469689	CV3452245	single nucleotide variant	NM_001130100.2(KIFC3):c.1247G>A (p.Ser416Asn)	not specified [RCV004636957]	uncertain significance	16	57766957	57766957	Human		name
597638244	CV3695374	single nucleotide variant	NM_001130100.2(KIFC3):c.1090G>A (p.Val364Ile)	not specified [RCV004941124]	uncertain significance	16	57769723	57769723	Human		name
597638265	CV3695379	single nucleotide variant	NM_001130100.2(KIFC3):c.2152G>A (p.Val718Met)	not specified [RCV004941128]	uncertain significance	16	57760806	57760806	Human		name
597638270	CV3695380	single nucleotide variant	NM_001130100.2(KIFC3):c.1790G>A (p.Arg597Gln)	not specified [RCV004941129]	uncertain significance	16	57761495	57761495	Human		name
597638273	CV3695381	single nucleotide variant	NM_001130100.2(KIFC3):c.1162C>G (p.Gln388Glu)	not specified [RCV004941130]	uncertain significance	16	57769651	57769651	Human		name
597768368	CV3695382	single nucleotide variant	NM_001130100.2(KIFC3):c.1267C>T (p.Arg423Cys)	not specified [RCV004927470]	uncertain significance	16	57766937	57766937	Human		name
598220712	CV3991152	single nucleotide variant	NM_001130100.2(KIFC3):c.2222T>C (p.Met741Thr)	not specified [RCV005360706]	uncertain significance	16	57760736	57760736	Human		name
598181975	CV3991153	single nucleotide variant	NM_001130100.2(KIFC3):c.1037C>G (p.Ala346Gly)	not specified [RCV005352635]	uncertain significance	16	57769858	57769858	Human		name

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