fut10 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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42 records found for search term fut10

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8650259	CV126834	single nucleotide variant	NM_032664.3(FUT10):c.-274+484G>T	Lung cancer [RCV000107321]	uncertain significance	8	33472580	33472580	Human		name
405784084	CV3257608	single nucleotide variant	NM_032664.3(FUT10):c.7C>T (p.Arg3Trp)	not specified [RCV004387302]	uncertain significance	8	33461446	33461446	Human		name
156155930	CV2266176	single nucleotide variant	NM_032664.3(FUT10):c.98G>T (p.Gly33Val)	not specified [RCV004128756]	uncertain significance	8	33453494	33453494	Human		name
597778821	CV3676750	single nucleotide variant	NM_032664.3(FUT10):c.79C>A (p.Gln27Lys)	not specified [RCV004930222]	uncertain significance	8	33461374	33461374	Human		name
155985181	CV2368064	single nucleotide variant	NM_032664.3(FUT10):c.193A>G (p.Lys65Glu)	not specified [RCV004216418]	uncertain significance	8	33453399	33453399	Human		name
401893105	CV2758941	single nucleotide variant	NM_032664.3(FUT10):c.151A>C (p.Lys51Gln)	not specified [RCV004342257]	uncertain significance	8	33453441	33453441	Human		name
407484954	CV3439361	single nucleotide variant	NM_032664.3(FUT10):c.135G>T (p.Leu45Phe)	not specified [RCV004618830]	uncertain significance	8	33453457	33453457	Human		name
598243275	CV3966744	single nucleotide variant	NM_032664.3(FUT10):c.271A>G (p.Thr91Ala)	not specified [RCV005344685]	uncertain significance	8	33453321	33453321	Human		name
156384682	CV2231157	single nucleotide variant	NM_032664.3(FUT10):c.743G>A (p.Arg248Gln)	not specified [RCV004094366]	uncertain significance	8	33389432	33389432	Human		name
155983620	CV2240759	single nucleotide variant	NM_032664.3(FUT10):c.793G>A (p.Asp265Asn)	not specified [RCV004119371]	uncertain significance	8	33389382	33389382	Human		name
156016349	CV2266331	single nucleotide variant	NM_032664.3(FUT10):c.574C>G (p.Leu192Val)	not specified [RCV004129151]	uncertain significance	8	33389601	33389601	Human		name
156086062	CV2289906	single nucleotide variant	NM_032664.3(FUT10):c.331C>T (p.Arg111Trp)	not specified [RCV004150562]	uncertain significance	8	33453261	33453261	Human		name
156001568	CV2296423	single nucleotide variant	NM_032664.3(FUT10):c.478C>T (p.His160Tyr)	not specified [RCV004148166]	uncertain significance	8	33389697	33389697	Human		name
156166125	CV2330101	single nucleotide variant	NM_032664.3(FUT10):c.412C>T (p.Arg138Trp)	not specified [RCV004185591]	uncertain significance	8	33389763	33389763	Human		name
156230415	CV2348679	single nucleotide variant	NM_032664.3(FUT10):c.304G>A (p.Ala102Thr)	not specified [RCV004201095]	uncertain significance	8	33453288	33453288	Human		name
329376511	CV2425110	single nucleotide variant	NM_032664.3(FUT10):c.314G>C (p.Cys105Ser)	not specified [RCV004249003]	uncertain significance	8	33453278	33453278	Human		name
401731903	CV2690197	single nucleotide variant	NM_032664.3(FUT10):c.488T>C (p.Val163Ala)	not specified [RCV004302206]	uncertain significance	8	33389687	33389687	Human		name
401733125	CV2691209	single nucleotide variant	NM_032664.3(FUT10):c.857A>G (p.Asp286Gly)	not specified [RCV004302983]	uncertain significance	8	33389318	33389318	Human		name
401781869	CV2722312	single nucleotide variant	NM_032664.3(FUT10):c.427G>T (p.Asp143Tyr)	not specified [RCV004322732]	uncertain significance	8	33389748	33389748	Human		name
401889613	CV2766756	single nucleotide variant	NM_032664.3(FUT10):c.919G>A (p.Gly307Arg)	not specified [RCV004349146]	uncertain significance	8	33389256	33389256	Human		name
405784065	CV3257605	single nucleotide variant	NM_032664.3(FUT10):c.302G>A (p.Gly101Glu)	not specified [RCV004387299]	uncertain significance	8	33453290	33453290	Human		name
405784072	CV3257606	single nucleotide variant	NM_032664.3(FUT10):c.452C>A (p.Ser151Tyr)	not specified [RCV004387300]	uncertain significance	8	33389723	33389723	Human		name
405784078	CV3257607	single nucleotide variant	NM_032664.3(FUT10):c.638C>T (p.Pro213Leu)	not specified [RCV004387301]	uncertain significance	8	33389537	33389537	Human		name
407484944	CV3439359	single nucleotide variant	NM_032664.3(FUT10):c.418G>A (p.Ala140Thr)	not specified [RCV004618828]	uncertain significance	8	33389757	33389757	Human		name
597778809	CV3676747	single nucleotide variant	NM_032664.3(FUT10):c.434C>T (p.Ala145Val)	not specified [RCV004930219]	uncertain significance	8	33389741	33389741	Human		name
597778813	CV3676748	single nucleotide variant	NM_032664.3(FUT10):c.665A>T (p.Asp222Val)	not specified [RCV004930220]	uncertain significance	8	33389510	33389510	Human		name
597778817	CV3676749	single nucleotide variant	NM_032664.3(FUT10):c.587G>A (p.Arg196Gln)	not specified [RCV004930221]	uncertain significance	8	33389588	33389588	Human		name
597778825	CV3676752	single nucleotide variant	NM_032664.3(FUT10):c.848C>T (p.Ala283Val)	not specified [RCV004930223]	uncertain significance	8	33389327	33389327	Human		name
597742557	CV3676755	single nucleotide variant	NM_032664.3(FUT10):c.563G>T (p.Ser188Ile)	not specified [RCV004921902]	uncertain significance	8	33389612	33389612	Human		name
597742565	CV3676756	single nucleotide variant	NM_032664.3(FUT10):c.757C>G (p.Pro253Ala)	not specified [RCV004921903]	uncertain significance	8	33389418	33389418	Human		name
156133587	CV2195963	single nucleotide variant	NM_032664.3(FUT10):c.1168A>G (p.Met390Val)	not specified [RCV004072217]	uncertain significance	8	33389007	33389007	Human		name
155980058	CV2336867	single nucleotide variant	NM_032664.3(FUT10):c.1189G>A (p.Ala397Thr)	not specified [RCV004190486]	uncertain significance	8	33388986	33388986	Human		name
156070640	CV2337697	single nucleotide variant	NM_032664.3(FUT10):c.1231T>C (p.Trp411Arg)	not specified [RCV004183725]	uncertain significance	8	33372786	33372786	Human		name
329387690	CV2470904	single nucleotide variant	NM_032664.3(FUT10):c.1171G>T (p.Val391Leu)	not specified [RCV004276101]	uncertain significance	8	33389004	33389004	Human		name
401880623	CV2780283	single nucleotide variant	NM_032664.3(FUT10):c.1345C>A (p.Gln449Lys)	not specified [RCV004355911]	uncertain significance	8	33372672	33372672	Human		name
405784417	CV3257604	single nucleotide variant	NM_032664.3(FUT10):c.1112G>T (p.Arg371Leu)	not specified [RCV004387298]	uncertain significance	8	33389063	33389063	Human		name
407484949	CV3439360	single nucleotide variant	NM_032664.3(FUT10):c.1027G>A (p.Asp343Asn)	not specified [RCV004618829]	uncertain significance	8	33389148	33389148	Human		name
597742552	CV3676751	single nucleotide variant	NM_032664.3(FUT10):c.1088G>A (p.Arg363Gln)	not specified [RCV004921901]	uncertain significance	8	33389087	33389087	Human		name
597778832	CV3676754	single nucleotide variant	NM_032664.3(FUT10):c.1352A>G (p.Lys451Arg)	not specified [RCV004930224]	uncertain significance	8	33372665	33372665	Human		name
597742571	CV3676757	single nucleotide variant	NM_032664.3(FUT10):c.1222C>T (p.Pro408Ser)	not specified [RCV004921904]	uncertain significance	8	33372795	33372795	Human		name
598243262	CV3966742	single nucleotide variant	NM_032664.3(FUT10):c.1291C>G (p.Leu431Val)	not specified [RCV005344683]	uncertain significance	8	33372726	33372726	Human		name
598243269	CV3966743	single nucleotide variant	NM_032664.3(FUT10):c.1153G>C (p.Asp385His)	not specified [RCV005344684]	uncertain significance	8	33389022	33389022	Human		name

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