Ddx51 Variant Search Result - Rat Genome Database

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107 records found for search term Ddx51

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401910011	CV2813718	single nucleotide variant	NM_175066.4(DDX51):c.186G>C (p.Pro62=)	not provided [RCV003398297]	likely benign	12	132144111	132144111	Human		name
155909374	CV2359693	single nucleotide variant	NM_175066.4(DDX51):c.56G>A (p.Gly19Glu)	not specified [RCV004210516]	uncertain significance	12	132144241	132144241	Human		name
401898397	CV2787855	single nucleotide variant	NM_175066.4(DDX51):c.59C>T (p.Pro20Leu)	not specified [RCV004358534]	uncertain significance	12	132144238	132144238	Human		name
405667764	CV3239962	single nucleotide variant	NM_175066.4(DDX51):c.94C>T (p.Arg32Cys)	not specified [RCV004368014]	uncertain significance	12	132144203	132144203	Human		name
407458834	CV3426651	single nucleotide variant	NM_175066.4(DDX51):c.86G>A (p.Gly29Asp)	not specified [RCV004611697]	uncertain significance	12	132144211	132144211	Human		name
597805739	CV3658348	single nucleotide variant	NM_175066.4(DDX51):c.79G>A (p.Ala27Thr)	not specified [RCV004908819]	uncertain significance	12	132144218	132144218	Human		name
598222800	CV3956381	single nucleotide variant	NM_175066.4(DDX51):c.73G>A (p.Ala25Thr)	not specified [RCV005317974]	uncertain significance	12	132144224	132144224	Human		name
598222805	CV3956382	single nucleotide variant	NM_175066.4(DDX51):c.95G>A (p.Arg32His)	not specified [RCV005317975]	uncertain significance	12	132144202	132144202	Human		name
15166203	CV713447	single nucleotide variant	NM_175066.4(DDX51):c.798C>T (p.Phe266=)	not provided [RCV000971122]	benign	12	132142295	132142295	Human		name
156162315	CV2246506	single nucleotide variant	NM_175066.4(DDX51):c.208C>T (p.Pro70Ser)	not specified [RCV004110263]	uncertain significance	12	132144089	132144089	Human		name
329371566	CV2432014	single nucleotide variant	NM_175066.4(DDX51):c.127C>T (p.Arg43Cys)	not specified [RCV004249166]	uncertain significance	12	132144170	132144170	Human		name
329385723	CV2432201	single nucleotide variant	NM_175066.4(DDX51):c.181G>C (p.Glu61Gln)	not specified [RCV004251133]	uncertain significance	12	132144116	132144116	Human		name
401910005	CV2813715	single nucleotide variant	NM_175066.4(DDX51):c.1686G>A (p.Thr562=)	not provided [RCV003398294]	likely benign	12	132140187	132140187	Human		name
401910007	CV2813716	single nucleotide variant	NM_175066.4(DDX51):c.1626C>T (p.Gly542=)	not provided [RCV003398295]	likely benign	12	132140470	132140470	Human		name
401910009	CV2813717	single nucleotide variant	NM_175066.4(DDX51):c.1515G>A (p.Ser505=)	not provided [RCV003398296]	likely benign	12	132140661	132140661	Human		name
405667653	CV3239939	single nucleotide variant	NM_175066.4(DDX51):c.145C>G (p.Arg49Gly)	not specified [RCV004367991]	uncertain significance	12	132144152	132144152	Human		name
405667720	CV3239953	single nucleotide variant	NM_175066.4(DDX51):c.214C>G (p.Arg72Gly)	not specified [RCV004368005]	uncertain significance	12	132144083	132144083	Human		name
407458831	CV3426650	single nucleotide variant	NM_175066.4(DDX51):c.170C>G (p.Ala57Gly)	not specified [RCV004611696]	uncertain significance	12	132144127	132144127	Human		name
407458853	CV3426657	single nucleotide variant	NM_175066.4(DDX51):c.106G>A (p.Glu36Lys)	not specified [RCV004611703]	uncertain significance	12	132144191	132144191	Human		name
156188284	CV2195864	single nucleotide variant	NM_175066.4(DDX51):c.743G>A (p.Arg248Gln)	not specified [RCV004076203]	likely benign	12	132142350	132142350	Human		name
155932900	CV2228760	single nucleotide variant	NM_175066.4(DDX51):c.985G>T (p.Val329Phe)	not specified [RCV004093229]	uncertain significance	12	132141860	132141860	Human		name
156204204	CV2234703	single nucleotide variant	NM_175066.4(DDX51):c.901T>C (p.Phe301Leu)	not specified [RCV004102651]	uncertain significance	12	132141944	132141944	Human		name
156033319	CV2236214	single nucleotide variant	NM_175066.4(DDX51):c.498C>A (p.Phe166Leu)	not specified [RCV004107919]	uncertain significance	12	132143716	132143716	Human		name
156197787	CV2237339	single nucleotide variant	NM_175066.4(DDX51):c.898G>C (p.Val300Leu)	not specified [RCV004104535]	uncertain significance	12	132141947	132141947	Human		name
156219827	CV2254091	single nucleotide variant	NM_175066.4(DDX51):c.583G>A (p.Asp195Asn)	not specified [RCV004129536]	uncertain significance	12	132142815	132142815	Human		name
156341625	CV2268291	single nucleotide variant	NM_175066.4(DDX51):c.466C>A (p.Pro156Thr)	not specified [RCV004138584]	uncertain significance	12	132143748	132143748	Human		name
156048916	CV2304465	single nucleotide variant	NM_175066.4(DDX51):c.988C>A (p.Gln330Lys)	not specified [RCV004164557]	uncertain significance	12	132141857	132141857	Human		name
155958894	CV2313848	single nucleotide variant	NM_175066.4(DDX51):c.616C>T (p.His206Tyr)	not specified [RCV004164168]	uncertain significance	12	132142782	132142782	Human		name
156270418	CV2315530	single nucleotide variant	NM_175066.4(DDX51):c.740A>G (p.Tyr247Cys)	not specified [RCV004169577]	uncertain significance	12	132142353	132142353	Human		name
155976613	CV2324771	single nucleotide variant	NM_175066.4(DDX51):c.913A>G (p.Thr305Ala)	not specified [RCV004173005]	uncertain significance	12	132141932	132141932	Human		name
155985938	CV2343987	single nucleotide variant	NM_175066.4(DDX51):c.413G>C (p.Ser138Thr)	not specified [RCV004195604]	uncertain significance	12	132143801	132143801	Human		name
156283559	CV2348948	single nucleotide variant	NM_175066.4(DDX51):c.841C>A (p.His281Asn)	not specified [RCV004203381]	uncertain significance	12	132142166	132142166	Human		name
156056616	CV2396259	single nucleotide variant	NM_175066.4(DDX51):c.742C>T (p.Arg248Trp)	not specified [RCV004240210]	uncertain significance	12	132142351	132142351	Human		name
329383118	CV2434405	single nucleotide variant	NM_175066.4(DDX51):c.926C>T (p.Pro309Leu)	not specified [RCV004254121]	uncertain significance	12	132141919	132141919	Human		name
329400235	CV2440813	single nucleotide variant	NM_175066.4(DDX51):c.727G>A (p.Gly243Ser)	not specified [RCV004258754]	uncertain significance	12	132142366	132142366	Human		name
329360015	CV2446523	single nucleotide variant	NM_175066.4(DDX51):c.593C>T (p.Pro198Leu)	not specified [RCV004251423]	uncertain significance	12	132142805	132142805	Human		name
401731496	CV2693834	single nucleotide variant	NM_175066.4(DDX51):c.418A>T (p.Ser140Cys)	not specified [RCV004300142]	uncertain significance	12	132143796	132143796	Human		name
401752470	CV2707020	single nucleotide variant	NM_175066.4(DDX51):c.506G>A (p.Arg169Lys)	not specified [RCV004321616]	uncertain significance	12	132143708	132143708	Human		name
401777126	CV2707737	single nucleotide variant	NM_175066.4(DDX51):c.607C>G (p.Pro203Ala)	not specified [RCV004306988]	uncertain significance	12	132142791	132142791	Human		name
401764573	CV2721390	single nucleotide variant	NM_175066.4(DDX51):c.985G>C (p.Val329Leu)	not specified [RCV004322138]	uncertain significance	12	132141860	132141860	Human		name
401874903	CV2781353	single nucleotide variant	NM_175066.4(DDX51):c.366G>C (p.Glu122Asp)	not specified [RCV004352362]	uncertain significance	12	132143848	132143848	Human		name
405667726	CV3239954	single nucleotide variant	NM_175066.4(DDX51):c.356C>T (p.Ala119Val)	not specified [RCV004368006]	uncertain significance	12	132143858	132143858	Human		name
405667731	CV3239955	single nucleotide variant	NM_175066.4(DDX51):c.527C>G (p.Pro176Arg)	not specified [RCV004368007]	uncertain significance	12	132142871	132142871	Human		name
405667734	CV3239956	single nucleotide variant	NM_175066.4(DDX51):c.538A>G (p.Arg180Gly)	not specified [RCV004368008]	uncertain significance	12	132142860	132142860	Human		name
405667739	CV3239957	single nucleotide variant	NM_175066.4(DDX51):c.625C>G (p.Leu209Val)	not specified [RCV004368009]	uncertain significance	12	132142773	132142773	Human		name
405667744	CV3239958	single nucleotide variant	NM_175066.4(DDX51):c.636G>C (p.Gln212His)	not specified [RCV004368010]	uncertain significance	12	132142762	132142762	Human		name
405667749	CV3239959	single nucleotide variant	NM_175066.4(DDX51):c.688C>T (p.Pro230Ser)	not specified [RCV004368011]	uncertain significance	12	132142405	132142405	Human		name
405667754	CV3239960	single nucleotide variant	NM_175066.4(DDX51):c.787A>G (p.Thr263Ala)	not specified [RCV004368012]	uncertain significance	12	132142306	132142306	Human		name
407458840	CV3426653	single nucleotide variant	NM_175066.4(DDX51):c.817G>A (p.Ala273Thr)	not specified [RCV004611699]	uncertain significance	12	132142190	132142190	Human		name
597805737	CV3658346	single nucleotide variant	NM_175066.4(DDX51):c.469C>G (p.Leu157Val)	not specified [RCV004908817]	uncertain significance	12	132143745	132143745	Human		name
598222774	CV3956377	single nucleotide variant	NM_175066.4(DDX51):c.491G>C (p.Gly164Ala)	not specified [RCV005317970]	uncertain significance	12	132143723	132143723	Human		name
598222780	CV3956378	single nucleotide variant	NM_175066.4(DDX51):c.311A>G (p.Asn104Ser)	not specified [RCV005317971]	likely benign	12	132143903	132143903	Human		name
598222789	CV3956379	single nucleotide variant	NM_175066.4(DDX51):c.305A>G (p.Glu102Gly)	not specified [RCV005317972]	uncertain significance	12	132143909	132143909	Human		name
150412267	CV1196095	single nucleotide variant	NM_175066.4(DDX51):c.1378G>A (p.Gly460Ser)	not provided [RCV001574026]	likely benign	12	132140893	132140893	Human		name
156067556	CV2193581	single nucleotide variant	NM_175066.4(DDX51):c.1269G>C (p.Met423Ile)	not specified [RCV004073054]	uncertain significance	12	132141002	132141002	Human		name
156141931	CV2199980	single nucleotide variant	NM_175066.4(DDX51):c.1096C>T (p.Arg366Cys)	not specified [RCV004074146]	uncertain significance	12	132141506	132141506	Human		name
155915579	CV2200399	single nucleotide variant	NM_175066.4(DDX51):c.1723G>C (p.Glu575Gln)	not specified [RCV004076721]	likely benign	12	132140150	132140150	Human		name
156190876	CV2206095	single nucleotide variant	NM_175066.4(DDX51):c.1543G>A (p.Glu515Lys)	not specified [RCV004078504]	uncertain significance	12	132140633	132140633	Human		name
156250378	CV2273276	single nucleotide variant	NM_175066.4(DDX51):c.1216C>G (p.Gln406Glu)	not specified [RCV004132069]	uncertain significance	12	132141309	132141309	Human		name
155996276	CV2277388	single nucleotide variant	NM_175066.4(DDX51):c.1246G>A (p.Ala416Thr)	not specified [RCV004144806]	uncertain significance	12	132141279	132141279	Human		name
155915433	CV2339127	single nucleotide variant	NM_175066.4(DDX51):c.1640T>A (p.Ile547Asn)	not specified [RCV004187168]	uncertain significance	12	132140456	132140456	Human		name
156085724	CV2340475	single nucleotide variant	NM_175066.4(DDX51):c.1207G>T (p.Ala403Ser)	not specified [RCV004197199]	uncertain significance	12	132141318	132141318	Human		name
156402030	CV2367866	single nucleotide variant	NM_175066.4(DDX51):c.1169C>T (p.Ala390Val)	not specified [RCV004222971]	uncertain significance	12	132141356	132141356	Human		name
155937337	CV2373545	single nucleotide variant	NM_175066.4(DDX51):c.1444C>T (p.His482Tyr)	not specified [RCV004222648]	uncertain significance	12	132140732	132140732	Human		name
156007415	CV2394355	single nucleotide variant	NM_175066.4(DDX51):c.1382T>C (p.Leu461Pro)	not specified [RCV004238574]	likely benign	12	132140889	132140889	Human		name
329369863	CV2424938	single nucleotide variant	NM_175066.4(DDX51):c.1934G>A (p.Arg645Gln)	not specified [RCV004248812]	uncertain significance	12	132139675	132139675	Human		name
329386668	CV2428374	single nucleotide variant	NM_175066.4(DDX51):c.1922C>T (p.Pro641Leu)	not specified [RCV004253182]	uncertain significance	12	132139687	132139687	Human		name
329370628	CV2435588	single nucleotide variant	NM_175066.4(DDX51):c.1805C>G (p.Thr602Ser)	not specified [RCV004254840]	uncertain significance	12	132139895	132139895	Human		name
329365850	CV2441159	single nucleotide variant	NM_175066.4(DDX51):c.1340A>G (p.His447Arg)	not specified [RCV004263558]	uncertain significance	12	132140931	132140931	Human		name
401746381	CV2694845	single nucleotide variant	NM_175066.4(DDX51):c.1711G>A (p.Val571Met)	not specified [RCV004300920]	uncertain significance	12	132140162	132140162	Human		name
401748995	CV2708438	single nucleotide variant	NM_175066.4(DDX51):c.1387G>C (p.Asp463His)	not specified [RCV004313539]	uncertain significance	12	132140884	132140884	Human		name
401742581	CV2715266	single nucleotide variant	NM_175066.4(DDX51):c.1370C>T (p.Ala457Val)	not specified [RCV004324609]	uncertain significance	12	132140901	132140901	Human		name
401780821	CV2723763	single nucleotide variant	NM_175066.4(DDX51):c.1213C>T (p.Leu405Phe)	not specified [RCV004325922]	likely benign	12	132141312	132141312	Human		name
401862578	CV2762235	single nucleotide variant	NM_175066.4(DDX51):c.1483G>A (p.Val495Ile)	not specified [RCV004335360]	likely benign	12	132140693	132140693	Human		name
401866156	CV2762547	single nucleotide variant	NM_175066.4(DDX51):c.1174G>A (p.Ala392Thr)	not specified [RCV004338080]	uncertain significance	12	132141351	132141351	Human		name
401897163	CV2789883	single nucleotide variant	NM_175066.4(DDX51):c.1777G>C (p.Val593Leu)	not specified [RCV004362267]	uncertain significance	12	132139923	132139923	Human		name
405667639	CV3239936	single nucleotide variant	NM_175066.4(DDX51):c.1363G>A (p.Gly455Arg)	not specified [RCV004367988]	uncertain significance	12	132140908	132140908	Human		name
405667644	CV3239937	single nucleotide variant	NM_175066.4(DDX51):c.1402G>A (p.Gly468Arg)	not specified [RCV004367989]	likely benign	12	132140869	132140869	Human		name
405667648	CV3239938	single nucleotide variant	NM_175066.4(DDX51):c.1448A>G (p.Tyr483Cys)	not specified [RCV004367990]	uncertain significance	12	132140728	132140728	Human		name
405667658	CV3239940	single nucleotide variant	NM_175066.4(DDX51):c.1492C>G (p.Leu498Val)	not specified [RCV004367992]	uncertain significance	12	132140684	132140684	Human		name
405667662	CV3239941	single nucleotide variant	NM_175066.4(DDX51):c.1496T>G (p.Val499Gly)	not specified [RCV004367993]	uncertain significance	12	132140680	132140680	Human		name
405667667	CV3239942	single nucleotide variant	NM_175066.4(DDX51):c.1541G>A (p.Arg514Gln)	not specified [RCV004367994]	uncertain significance	12	132140635	132140635	Human		name
405667672	CV3239943	single nucleotide variant	NM_175066.4(DDX51):c.1568T>G (p.Leu523Arg)	not specified [RCV004367995]	uncertain significance	12	132140528	132140528	Human		name
405667677	CV3239944	single nucleotide variant	NM_175066.4(DDX51):c.1618G>A (p.Gly540Arg)	not specified [RCV004367996]	uncertain significance	12	132140478	132140478	Human		name
405667686	CV3239946	single nucleotide variant	NM_175066.4(DDX51):c.1741G>A (p.Asp581Asn)	not specified [RCV004367998]	uncertain significance	12	132140132	132140132	Human		name
405667692	CV3239947	single nucleotide variant	NM_175066.4(DDX51):c.1744G>A (p.Ala582Thr)	not specified [RCV004367999]	uncertain significance	12	132140129	132140129	Human		name
405667696	CV3239948	single nucleotide variant	NM_175066.4(DDX51):c.1763C>T (p.Thr588Ile)	not specified [RCV004368000]	uncertain significance	12	132140110	132140110	Human		name
405667701	CV3239949	single nucleotide variant	NM_175066.4(DDX51):c.1879C>T (p.Pro627Ser)	not specified [RCV004368001]	uncertain significance	12	132139730	132139730	Human		name
405667705	CV3239950	single nucleotide variant	NM_175066.4(DDX51):c.1891C>T (p.Arg631Trp)	not specified [RCV004368002]	uncertain significance	12	132139718	132139718	Human		name
405667715	CV3239952	single nucleotide variant	NM_175066.4(DDX51):c.1904C>T (p.Ser635Phe)	not specified [RCV004368004]	uncertain significance	12	132139705	132139705	Human		name
407458837	CV3426652	single nucleotide variant	NM_175066.4(DDX51):c.1124G>A (p.Arg375Gln)	not specified [RCV004611698]	uncertain significance	12	132141401	132141401	Human		name
407458847	CV3426655	single nucleotide variant	NM_175066.4(DDX51):c.1196C>T (p.Ala399Val)	not specified [RCV004611701]	uncertain significance	12	132141329	132141329	Human		name
407458849	CV3426656	single nucleotide variant	NM_175066.4(DDX51):c.1229C>T (p.Ala410Val)	not specified [RCV004611702]	uncertain significance	12	132141296	132141296	Human		name
407458856	CV3426658	single nucleotide variant	NM_175066.4(DDX51):c.1897G>A (p.Glu633Lys)	not specified [RCV004611704]	uncertain significance	12	132139712	132139712	Human		name
597805738	CV3658347	single nucleotide variant	NM_175066.4(DDX51):c.1409C>T (p.Ser470Leu)	not specified [RCV004908818]	uncertain significance	12	132140862	132140862	Human		name
597805740	CV3658349	single nucleotide variant	NM_175066.4(DDX51):c.1195G>C (p.Ala399Pro)	not specified [RCV004908820]	uncertain significance	12	132141330	132141330	Human		name
597805741	CV3658350	single nucleotide variant	NM_175066.4(DDX51):c.1768G>A (p.Val590Met)	not specified [RCV004908821]	uncertain significance	12	132140105	132140105	Human		name
597805742	CV3658351	single nucleotide variant	NM_175066.4(DDX51):c.1378G>T (p.Gly460Cys)	not specified [RCV004908822]	uncertain significance	12	132140893	132140893	Human		name
597805743	CV3658352	single nucleotide variant	NM_175066.4(DDX51):c.1224G>T (p.Arg408Ser)	not specified [RCV004908823]	uncertain significance	12	132141301	132141301	Human		name
597805744	CV3658353	single nucleotide variant	NM_175066.4(DDX51):c.1111G>A (p.Asp371Asn)	not specified [RCV004908824]	uncertain significance	12	132141414	132141414	Human		name
597805745	CV3658354	single nucleotide variant	NM_175066.4(DDX51):c.1307A>C (p.Gln436Pro)	not specified [RCV004908825]	uncertain significance	12	132140964	132140964	Human		name
597805746	CV3658355	single nucleotide variant	NM_175066.4(DDX51):c.1312C>G (p.Pro438Ala)	not specified [RCV004908826]	uncertain significance	12	132140959	132140959	Human		name
597805747	CV3658356	single nucleotide variant	NM_175066.4(DDX51):c.1089G>T (p.Gln363His)	not specified [RCV004908827]	uncertain significance	12	132141513	132141513	Human		name
598222756	CV3956374	single nucleotide variant	NM_175066.4(DDX51):c.1220G>A (p.Arg407Gln)	not specified [RCV005317967]	uncertain significance	12	132141305	132141305	Human		name
598222762	CV3956375	single nucleotide variant	NM_175066.4(DDX51):c.1159C>T (p.Arg387Trp)	not specified [RCV005317968]	uncertain significance	12	132141366	132141366	Human		name
598222769	CV3956376	single nucleotide variant	NM_175066.4(DDX51):c.1105A>G (p.Ile369Val)	not specified [RCV005317969]	likely benign	12	132141420	132141420	Human		name
598222794	CV3956380	single nucleotide variant	NM_175066.4(DDX51):c.1024A>G (p.Ile342Val)	not specified [RCV005317973]	uncertain significance	12	132141578	132141578	Human		name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

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Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
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MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

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