Ddx50 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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61 records found for search term Ddx50

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155953357	CV2379001	single nucleotide variant	NM_024045.2(DDX50):c.20G>C (p.Trp7Ser)	not specified [RCV004233763]	uncertain significance	10	68901404	68901404	Human		name
329373402	CV2434218	single nucleotide variant	NM_024045.2(DDX50):c.55G>A (p.Glu19Lys)	not specified [RCV004250105]	uncertain significance	10	68901439	68901439	Human		name
401783759	CV2723921	single nucleotide variant	NM_024045.2(DDX50):c.47C>T (p.Pro16Leu)	not specified [RCV004327833]	uncertain significance	10	68901431	68901431	Human		name
405667627	CV3239934	single nucleotide variant	NM_024045.2(DDX50):c.73A>G (p.Lys25Glu)	not specified [RCV004367986]	uncertain significance	10	68901457	68901457	Human		name
407458822	CV3426647	single nucleotide variant	NM_024045.2(DDX50):c.68A>C (p.Gln23Pro)	not specified [RCV004611693]	uncertain significance	10	68901452	68901452	Human		name
407458825	CV3426648	single nucleotide variant	NM_024045.2(DDX50):c.71A>T (p.Lys24Met)	not specified [RCV004611694]	uncertain significance	10	68901455	68901455	Human		name
15164529	CV724020	single nucleotide variant	NM_024045.2(DDX50):c.717C>T (p.Ser239=)	not provided [RCV000882214]	benign	10	68913239	68913239	Human		name
156143603	CV2208652	single nucleotide variant	NM_024045.2(DDX50):c.111C>A (p.His37Gln)	not specified [RCV004091166]	uncertain significance	10	68906734	68906734	Human		name
10767432	CV221016	single nucleotide variant	NM_024045.2(DDX50):c.122C>T (p.Ser41Leu)	Prostate cancer [RCV000204703]	uncertain significance	10	68906745	68906745	Human	2	name
156074392	CV2248171	single nucleotide variant	NM_024045.2(DDX50):c.164A>C (p.Asp55Ala)	not specified [RCV004117567]	uncertain significance	10	68906787	68906787	Human		name
405705642	CV3239925	single nucleotide variant	NM_024045.2(DDX50):c.165C>G (p.Asp55Glu)	not specified [RCV004375872]	uncertain significance	10	68906788	68906788	Human		name
405705650	CV3239926	single nucleotide variant	NM_024045.2(DDX50):c.197T>C (p.Met66Thr)	not specified [RCV004375873]	uncertain significance	10	68906820	68906820	Human		name
405667610	CV3239930	single nucleotide variant	NM_024045.2(DDX50):c.229G>C (p.Gly77Arg)	not specified [RCV004367982]	uncertain significance	10	68906852	68906852	Human		name
155903002	CV2301559	single nucleotide variant	NM_024045.2(DDX50):c.302T>C (p.Ile101Thr)	not specified [RCV004162468]	uncertain significance	10	68906925	68906925	Human		name
156249472	CV2314160	single nucleotide variant	NM_024045.2(DDX50):c.407A>G (p.Glu136Gly)	not specified [RCV004166245]	uncertain significance	10	68910329	68910329	Human		name
155927547	CV2349631	single nucleotide variant	NM_024045.2(DDX50):c.956A>G (p.Asn319Ser)	not specified [RCV004204051]	uncertain significance	10	68914071	68914071	Human		name
155931549	CV2370944	single nucleotide variant	NM_024045.2(DDX50):c.658A>G (p.Thr220Ala)	not specified [RCV004218671]	uncertain significance	10	68913180	68913180	Human		name
156142555	CV2386129	single nucleotide variant	NM_024045.2(DDX50):c.413C>G (p.Ala138Gly)	not specified [RCV004229180]	uncertain significance	10	68910335	68910335	Human		name
156156345	CV2393464	single nucleotide variant	NM_024045.2(DDX50):c.632C>T (p.Ser211Leu)	not specified [RCV004228956]	uncertain significance	10	68911239	68911239	Human		name
329399412	CV2470086	single nucleotide variant	NM_024045.2(DDX50):c.532A>G (p.Ile178Val)	not specified [RCV004287348]	uncertain significance	10	68911139	68911139	Human		name
401737999	CV2700887	single nucleotide variant	NM_024045.2(DDX50):c.413C>A (p.Ala138Asp)	not specified [RCV004307154]	uncertain significance	10	68910335	68910335	Human		name
401761228	CV2706264	single nucleotide variant	NM_024045.2(DDX50):c.700A>G (p.Ile234Val)	not specified [RCV004314929]	uncertain significance	10	68913222	68913222	Human		name
401891905	CV2775785	single nucleotide variant	NM_024045.2(DDX50):c.854G>A (p.Arg285Gln)	not specified [RCV004344832]	uncertain significance	10	68913487	68913487	Human		name
405667615	CV3239931	single nucleotide variant	NM_024045.2(DDX50):c.350C>G (p.Ser117Cys)	not specified [RCV004367983]	uncertain significance	10	68906973	68906973	Human		name
405667619	CV3239932	single nucleotide variant	NM_024045.2(DDX50):c.544C>T (p.Arg182Trp)	not specified [RCV004367984]	uncertain significance	10	68911151	68911151	Human		name
405667624	CV3239933	single nucleotide variant	NM_024045.2(DDX50):c.628C>T (p.Arg210Cys)	not specified [RCV004367985]	uncertain significance	10	68911235	68911235	Human		name
405667632	CV3239935	single nucleotide variant	NM_024045.2(DDX50):c.873A>T (p.Glu291Asp)	not specified [RCV004367987]	uncertain significance	10	68913506	68913506	Human		name
407458828	CV3426649	single nucleotide variant	NM_024045.2(DDX50):c.650T>C (p.Leu217Ser)	not specified [RCV004611695]	uncertain significance	10	68913172	68913172	Human		name
597805735	CV3658344	single nucleotide variant	NM_024045.2(DDX50):c.475T>C (p.Tyr159His)	not specified [RCV004908815]	uncertain significance	10	68911082	68911082	Human		name
597805736	CV3658345	single nucleotide variant	NM_024045.2(DDX50):c.445A>C (p.Ile149Leu)	not specified [RCV004908816]	uncertain significance	10	68910367	68910367	Human		name
597805733	CV3662226	single nucleotide variant	NM_024045.2(DDX50):c.395G>A (p.Arg132His)	not specified [RCV004908813]	uncertain significance	10	68910317	68910317	Human		name
597783155	CV3662228	single nucleotide variant	NM_024045.2(DDX50):c.833G>A (p.Arg278Gln)	not specified [RCV004900172]	uncertain significance	10	68913466	68913466	Human		name
598222719	CV3956368	single nucleotide variant	NM_024045.2(DDX50):c.806G>C (p.Arg269Pro)	not specified [RCV005317961]	uncertain significance	10	68913439	68913439	Human		name
598222750	CV3956373	single nucleotide variant	NM_024045.2(DDX50):c.656C>T (p.Pro219Leu)	not specified [RCV005317966]	uncertain significance	10	68913178	68913178	Human		name
156188999	CV2205881	single nucleotide variant	NM_024045.2(DDX50):c.2057G>A (p.Arg686Gln)	not specified [RCV004078318]	uncertain significance	10	68946473	68946473	Human		name
156330327	CV2226983	single nucleotide variant	NM_024045.2(DDX50):c.2188G>A (p.Gly730Arg)	not specified [RCV004097377]	uncertain significance	10	68946604	68946604	Human		name
155945452	CV2292104	single nucleotide variant	NM_024045.2(DDX50):c.1174G>T (p.Ala392Ser)	not specified [RCV004160368]	uncertain significance	10	68919916	68919916	Human		name
156087970	CV2295470	single nucleotide variant	NM_024045.2(DDX50):c.2122G>A (p.Gly708Arg)	not specified [RCV004160585]	uncertain significance	10	68946538	68946538	Human		name
156194023	CV2322022	single nucleotide variant	NM_024045.2(DDX50):c.1993G>A (p.Glu665Lys)	not specified [RCV004173775]	uncertain significance	10	68946409	68946409	Human		name
156034233	CV2338628	single nucleotide variant	NM_024045.2(DDX50):c.2087G>A (p.Arg696Gln)	not specified [RCV004182212]	uncertain significance	10	68946503	68946503	Human		name
155921511	CV2350679	single nucleotide variant	NM_024045.2(DDX50):c.2053G>C (p.Gly685Arg)	not specified [RCV004207028]	uncertain significance	10	68946469	68946469	Human		name
401742422	CV2673779	single nucleotide variant	NM_024045.2(DDX50):c.1558A>G (p.Met520Val)	not specified [RCV004293166]	uncertain significance	10	68936042	68936042	Human		name
401780427	CV2674020	single nucleotide variant	NM_024045.2(DDX50):c.2002T>G (p.Tyr668Asp)	not specified [RCV004293385]	uncertain significance	10	68946418	68946418	Human		name
401734613	CV2688575	single nucleotide variant	NM_024045.2(DDX50):c.1528A>G (p.Thr510Ala)	not specified [RCV004301533]	uncertain significance	10	68936012	68936012	Human		name
401732897	CV2691143	single nucleotide variant	NM_024045.2(DDX50):c.1415A>G (p.Tyr472Cys)	not specified [RCV004301137]	uncertain significance	10	68934812	68934812	Human		name
401771160	CV2726384	single nucleotide variant	NM_024045.2(DDX50):c.1883G>C (p.Gly628Ala)	not specified [RCV004328599]	uncertain significance	10	68941187	68941187	Human		name
401761372	CV2726737	single nucleotide variant	NM_024045.2(DDX50):c.1200G>T (p.Lys400Asn)	not specified [RCV004323064]	uncertain significance	10	68919942	68919942	Human		name
401891960	CV2775848	single nucleotide variant	NM_024045.2(DDX50):c.1883G>A (p.Gly628Glu)	not specified [RCV004344884]	uncertain significance	10	68941187	68941187	Human		name
405667596	CV3239927	single nucleotide variant	NM_024045.2(DDX50):c.2087G>T (p.Arg696Leu)	not specified [RCV004367979]	uncertain significance	10	68946503	68946503	Human		name
405667601	CV3239928	single nucleotide variant	NM_024045.2(DDX50):c.2095G>A (p.Gly699Ser)	not specified [RCV004367980]	uncertain significance	10	68946511	68946511	Human		name
405667605	CV3239929	single nucleotide variant	NM_024045.2(DDX50):c.2108G>A (p.Arg703Lys)	not specified [RCV004367981]	uncertain significance	10	68946524	68946524	Human		name
407458813	CV3426644	single nucleotide variant	NM_024045.2(DDX50):c.1844A>C (p.Asn615Thr)	not specified [RCV004611690]	uncertain significance	10	68941148	68941148	Human		name
407458816	CV3426645	single nucleotide variant	NM_024045.2(DDX50):c.2171G>C (p.Arg724Thr)	not specified [RCV004611691]	uncertain significance	10	68946587	68946587	Human		name
597805732	CV3662225	single nucleotide variant	NM_024045.2(DDX50):c.1928G>A (p.Arg643Lys)	not specified [RCV004908812]	uncertain significance	10	68943250	68943250	Human		name
597805734	CV3662227	single nucleotide variant	NM_024045.2(DDX50):c.1423C>T (p.Arg475Cys)	not specified [RCV004908814]	uncertain significance	10	68934820	68934820	Human		name
598222707	CV3956366	single nucleotide variant	NM_024045.2(DDX50):c.1217C>G (p.Ala406Gly)	not specified [RCV005317959]	uncertain significance	10	68919959	68919959	Human		name
598222712	CV3956367	single nucleotide variant	NM_024045.2(DDX50):c.2147A>G (p.Asp716Gly)	not specified [RCV005317960]	uncertain significance	10	68946563	68946563	Human		name
598222732	CV3956370	single nucleotide variant	NM_024045.2(DDX50):c.1989A>C (p.Glu663Asp)	not specified [RCV005317963]	uncertain significance	10	68946405	68946405	Human		name
598222738	CV3956371	single nucleotide variant	NM_024045.2(DDX50):c.1594A>G (p.Arg532Gly)	not specified [RCV005317964]	uncertain significance	10	68936078	68936078	Human		name
598222744	CV3956372	single nucleotide variant	NM_024045.2(DDX50):c.1439G>A (p.Gly480Asp)	not specified [RCV005317965]	uncertain significance	10	68934836	68934836	Human		name
15196924	CV724021	single nucleotide variant	NM_024045.2(DDX50):c.1975G>A (p.Ala659Thr)	not provided [RCV000889907]	benign	10	68946391	68946391	Human		name

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