Fut11 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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68 records found for search term Fut11

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401768658	CV2735382	single nucleotide variant	NM_173540.3(FUT11):c.20G>A (p.Arg7Lys)	not specified [RCV004334035]	uncertain significance	10	73772353	73772353	Human		name
401884604	CV2755915	single nucleotide variant	NM_173540.3(FUT11):c.14C>T (p.Pro5Leu)	not specified [RCV004336004]	uncertain significance	10	73772347	73772347	Human		name
15196661	CV767972	single nucleotide variant	NM_173540.3(FUT11):c.288C>A (p.Ile96=)	not provided [RCV000934283]	likely benign	10	73772621	73772621	Human		name
401780931	CV2734024	single nucleotide variant	NM_173540.3(FUT11):c.61G>A (p.Ala21Thr)	not specified [RCV004330586]	uncertain significance	10	73772394	73772394	Human		name
405784126	CV3257614	single nucleotide variant	NM_173540.3(FUT11):c.50G>A (p.Ser17Asn)	not specified [RCV004387308]	uncertain significance	10	73772383	73772383	Human		name
597742596	CV3676762	single nucleotide variant	NM_173540.3(FUT11):c.85G>A (p.Glu29Lys)	not specified [RCV004921908]	uncertain significance	10	73772418	73772418	Human		name
597742622	CV3676768	single nucleotide variant	NM_173540.3(FUT11):c.74G>C (p.Gly25Ala)	not specified [RCV004921912]	uncertain significance	10	73772407	73772407	Human		name
155927000	CV2208342	single nucleotide variant	NM_173540.3(FUT11):c.213G>C (p.Glu71Asp)	not specified [RCV004088775]	uncertain significance	10	73772546	73772546	Human		name
156136026	CV2213567	single nucleotide variant	NM_173540.3(FUT11):c.139T>C (p.Phe47Leu)	not specified [RCV004087519]	uncertain significance	10	73772472	73772472	Human		name
155951573	CV2309708	single nucleotide variant	NM_173540.3(FUT11):c.225G>C (p.Leu75Phe)	not specified [RCV004160841]	uncertain significance	10	73772558	73772558	Human		name
156283072	CV2360541	single nucleotide variant	NM_173540.3(FUT11):c.121C>A (p.Pro41Thr)	not specified [RCV004211301]	uncertain significance	10	73772454	73772454	Human		name
401721618	CV2683589	single nucleotide variant	NM_173540.3(FUT11):c.179G>A (p.Arg60His)	not specified [RCV004282516]	uncertain significance	10	73772512	73772512	Human		name
401733880	CV2697543	single nucleotide variant	NM_173540.3(FUT11):c.274G>A (p.Asp92Asn)	not specified [RCV004298302]	uncertain significance	10	73772607	73772607	Human		name
405784090	CV3257609	single nucleotide variant	NM_173540.3(FUT11):c.107C>T (p.Ala36Val)	not specified [RCV004387303]	uncertain significance	10	73772440	73772440	Human		name
405784105	CV3257611	single nucleotide variant	NM_173540.3(FUT11):c.169G>A (p.Gly57Arg)	not specified [RCV004387305]	uncertain significance	10	73772502	73772502	Human		name
405784113	CV3257612	single nucleotide variant	NM_173540.3(FUT11):c.202G>A (p.Gly68Arg)	not specified [RCV004387306]	uncertain significance	10	73772535	73772535	Human		name
597742589	CV3676761	single nucleotide variant	NM_173540.3(FUT11):c.197G>A (p.Arg66Gln)	not specified [RCV004921907]	uncertain significance	10	73772530	73772530	Human		name
598243284	CV3966746	single nucleotide variant	NM_173540.3(FUT11):c.142C>G (p.Arg48Gly)	not specified [RCV005344687]	uncertain significance	10	73772475	73772475	Human		name
598243300	CV3966750	single nucleotide variant	NM_173540.3(FUT11):c.262C>G (p.His88Asp)	not specified [RCV005344690]	uncertain significance	10	73772595	73772595	Human		name
598243314	CV3966753	single nucleotide variant	NM_173540.3(FUT11):c.182G>A (p.Ser61Asn)	not specified [RCV005344693]	uncertain significance	10	73772515	73772515	Human		name
156331230	CV2218131	single nucleotide variant	NM_173540.3(FUT11):c.566A>G (p.Tyr189Cys)	not specified [RCV004086559]	uncertain significance	10	73772899	73772899	Human		name
156278695	CV2227606	single nucleotide variant	NM_173540.3(FUT11):c.971T>C (p.Ile324Thr)	not specified [RCV004094026]	uncertain significance	10	73773452	73773452	Human		name
156135397	CV2347255	single nucleotide variant	NM_173540.3(FUT11):c.739C>T (p.Arg247Trp)	not specified [RCV004204722]	uncertain significance	10	73773220	73773220	Human		name
156392228	CV2378401	single nucleotide variant	NM_173540.3(FUT11):c.395C>T (p.Ala132Val)	not specified [RCV004226420]	uncertain significance	10	73772728	73772728	Human		name
155961914	CV2388145	single nucleotide variant	NM_173540.3(FUT11):c.593T>C (p.Met198Thr)	not specified [RCV004241261]	uncertain significance	10	73772926	73772926	Human		name
329400676	CV2438646	single nucleotide variant	NM_173540.3(FUT11):c.331G>A (p.Ala111Thr)	not specified [RCV004261811]	uncertain significance	10	73772664	73772664	Human		name
401733277	CV2685478	single nucleotide variant	NM_173540.3(FUT11):c.377A>C (p.Asp126Ala)	not specified [RCV004294501]	uncertain significance	10	73772710	73772710	Human		name
401749483	CV2712370	single nucleotide variant	NM_173540.3(FUT11):c.320G>A (p.Arg107Gln)	not specified [RCV004313853]	uncertain significance	10	73772653	73772653	Human		name
401738431	CV2714456	single nucleotide variant	NM_173540.3(FUT11):c.610C>G (p.Arg204Gly)	not specified [RCV004317982]	uncertain significance	10	73772943	73772943	Human		name
401754875	CV2717564	single nucleotide variant	NM_173540.3(FUT11):c.655G>T (p.Asp219Tyr)	not specified [RCV004330280]	uncertain significance	10	73772988	73772988	Human		name
401884430	CV2761729	single nucleotide variant	NM_173540.3(FUT11):c.370G>A (p.Gly124Ser)	not specified [RCV004337339]	uncertain significance	10	73772703	73772703	Human		name
405784119	CV3257613	single nucleotide variant	NM_173540.3(FUT11):c.499C>G (p.Leu167Val)	not specified [RCV004387307]	uncertain significance	10	73772832	73772832	Human		name
405784133	CV3257615	single nucleotide variant	NM_173540.3(FUT11):c.692T>G (p.Leu231Arg)	not specified [RCV004387309]	uncertain significance	10	73773025	73773025	Human		name
405784139	CV3257616	single nucleotide variant	NM_173540.3(FUT11):c.938A>C (p.Asp313Ala)	not specified [RCV004387310]	uncertain significance	10	73773419	73773419	Human		name
407484964	CV3439363	single nucleotide variant	NM_173540.3(FUT11):c.378C>A (p.Asp126Glu)	not specified [RCV004618832]	uncertain significance	10	73772711	73772711	Human		name
407484969	CV3439364	single nucleotide variant	NM_173540.3(FUT11):c.383G>A (p.Arg128His)	not specified [RCV004618833]	uncertain significance	10	73772716	73772716	Human		name
407484977	CV3439365	single nucleotide variant	NM_173540.3(FUT11):c.454A>G (p.Asn152Asp)	not specified [RCV004618834]	uncertain significance	10	73772787	73772787	Human		name
597742602	CV3676763	single nucleotide variant	NM_173540.3(FUT11):c.695T>C (p.Met232Thr)	not specified [RCV004921909]	uncertain significance	10	73773028	73773028	Human		name
597778840	CV3676765	single nucleotide variant	NM_173540.3(FUT11):c.929C>A (p.Ser310Tyr)	not specified [RCV004930226]	uncertain significance	10	73773410	73773410	Human		name
597742615	CV3676767	single nucleotide variant	NM_173540.3(FUT11):c.592A>G (p.Met198Val)	not specified [RCV004921911]	uncertain significance	10	73772925	73772925	Human		name
597778844	CV3676769	single nucleotide variant	NM_173540.3(FUT11):c.545A>G (p.Gln182Arg)	not specified [RCV004930227]	uncertain significance	10	73772878	73772878	Human		name
598243289	CV3966747	single nucleotide variant	NM_173540.3(FUT11):c.613C>T (p.Arg205Cys)	not specified [RCV005344688]	uncertain significance	10	73772946	73772946	Human		name
598158652	CV3966748	single nucleotide variant	NM_173540.3(FUT11):c.856A>G (p.Asn286Asp)	not specified [RCV005328089]	likely benign	10	73773337	73773337	Human		name
598243293	CV3966749	single nucleotide variant	NM_173540.3(FUT11):c.752C>T (p.Thr251Ile)	not specified [RCV005344689]	uncertain significance	10	73773233	73773233	Human		name
598243310	CV3966752	single nucleotide variant	NM_173540.3(FUT11):c.428C>T (p.Ala143Val)	not specified [RCV005344692]	uncertain significance	10	73772761	73772761	Human		name
15116358	CV712468	single nucleotide variant	NM_173540.3(FUT11):c.560C>G (p.Thr187Ser)	not provided [RCV000962020]	benign	10	73772893	73772893	Human		name
156185914	CV2232593	single nucleotide variant	NM_173540.3(FUT11):c.1222T>G (p.Ser408Ala)	not specified [RCV004101271]	uncertain significance	10	73773703	73773703	Human		name
156221881	CV2232594	single nucleotide variant	NM_173540.3(FUT11):c.1387G>A (p.Ala463Thr)	not specified [RCV004101272]	uncertain significance	10	73775593	73775593	Human		name
156360027	CV2254172	single nucleotide variant	NM_173540.3(FUT11):c.1150C>G (p.Leu384Val)	not specified [RCV004129854]	uncertain significance	10	73773631	73773631	Human		name
155990205	CV2276435	single nucleotide variant	NM_173540.3(FUT11):c.1177G>T (p.Asp393Tyr)	not specified [RCV004144161]	uncertain significance	10	73773658	73773658	Human		name
156037368	CV2313491	single nucleotide variant	NM_173540.3(FUT11):c.1100G>C (p.Ser367Thr)	not specified [RCV004163797]	uncertain significance	10	73773581	73773581	Human		name
155970272	CV2335564	single nucleotide variant	NM_173540.3(FUT11):c.1193G>A (p.Arg398Gln)	not specified [RCV004193775]	uncertain significance	10	73773674	73773674	Human		name
155916032	CV2336072	single nucleotide variant	NM_173540.3(FUT11):c.1154A>G (p.Asn385Ser)	not specified [RCV004189672]	uncertain significance	10	73773635	73773635	Human		name
329377603	CV2449839	single nucleotide variant	NM_173540.3(FUT11):c.1112G>C (p.Arg371Pro)	not specified [RCV004268934]	uncertain significance	10	73773593	73773593	Human		name
401746961	CV2692031	single nucleotide variant	NM_173540.3(FUT11):c.1216G>A (p.Ala406Thr)	not specified [RCV004301755]	uncertain significance	10	73773697	73773697	Human		name
401773082	CV2709112	single nucleotide variant	NM_173540.3(FUT11):c.1474C>A (p.Leu492Ile)	not specified [RCV004314443]	uncertain significance	10	73775680	73775680	Human		name
401770372	CV2711120	single nucleotide variant	NM_173540.3(FUT11):c.1034A>G (p.Glu345Gly)	not specified [RCV004310801]	uncertain significance	10	73773515	73773515	Human		name
401896060	CV2777367	single nucleotide variant	NM_173540.3(FUT11):c.1219G>C (p.Ala407Pro)	not specified [RCV004354375]	uncertain significance	10	73773700	73773700	Human		name
401864870	CV2791397	single nucleotide variant	NM_173540.3(FUT11):c.1240G>A (p.Val414Ile)	not specified [RCV004358795]	likely benign	10	73773721	73773721	Human		name
405784099	CV3257610	single nucleotide variant	NM_173540.3(FUT11):c.1270C>T (p.His424Tyr)	not specified [RCV004387304]	uncertain significance	10	73773751	73773751	Human		name
405854868	CV3394984	single nucleotide variant	NM_173540.3(FUT11):c.1035G>C (p.Glu345Asp)	not provided [RCV004555125]	uncertain significance	10	73773516	73773516	Human		name
407484960	CV3439362	single nucleotide variant	NM_173540.3(FUT11):c.1280G>A (p.Cys427Tyr)	not specified [RCV004618831]	uncertain significance	10	73773761	73773761	Human		name
597778836	CV3676758	single nucleotide variant	NM_173540.3(FUT11):c.1129G>C (p.Asp377His)	not specified [RCV004930225]	uncertain significance	10	73773610	73773610	Human		name
597742577	CV3676759	single nucleotide variant	NM_173540.3(FUT11):c.1282C>T (p.Pro428Ser)	not specified [RCV004921905]	uncertain significance	10	73773763	73773763	Human		name
597742583	CV3676760	single nucleotide variant	NM_173540.3(FUT11):c.1192C>T (p.Arg398Trp)	not specified [RCV004921906]	uncertain significance	10	73773673	73773673	Human		name
597742609	CV3676766	single nucleotide variant	NM_173540.3(FUT11):c.1217C>G (p.Ala406Gly)	not specified [RCV004921910]	uncertain significance	10	73773698	73773698	Human		name
598243305	CV3966751	single nucleotide variant	NM_173540.3(FUT11):c.1252C>G (p.His418Asp)	not specified [RCV005344691]	uncertain significance	10	73773733	73773733	Human		name
15191606	CV737595	single nucleotide variant	NM_173540.3(FUT11):c.1199A>G (p.Asp400Gly)	not provided [RCV000910296]	benign	10	73773680	73773680	Human		name

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