Ddx51 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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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

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Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

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