Ddx46 Variant Search Result - Rat Genome Database

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18 records found for search term Ddx46

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8631378	CV86539	single nucleotide variant	NM_014829.3(DDX46):c.1638C>T (p.Ile546=)	Malignant melanoma [RCV000066630]	not provided	5	134794861	134794861	Human		name
156380606	CV2218840	single nucleotide variant	NM_001300860.2(DDX46):c.231C>G (p.Asp77Glu)	not specified [RCV004085081]	uncertain significance	5	134766941	134766941	Human		name
155977189	CV2324951	single nucleotide variant	NM_001300860.2(DDX46):c.229G>T (p.Asp77Tyr)	not specified [RCV004175206]	uncertain significance	5	134766939	134766939	Human		name
156020048	CV2230221	single nucleotide variant	NM_001300860.2(DDX46):c.761A>G (p.Glu254Gly)	not specified [RCV004099847]	uncertain significance	5	134777721	134777721	Human		name
407458747	CV3426622	single nucleotide variant	NM_001300860.2(DDX46):c.779C>T (p.Thr260Met)	not specified [RCV004611668]	uncertain significance	5	134781146	134781146	Human		name
407458750	CV3426623	single nucleotide variant	NM_001300860.2(DDX46):c.532G>A (p.Ala178Thr)	not specified [RCV004611669]	uncertain significance	5	134773780	134773780	Human		name
597805714	CV3662205	single nucleotide variant	NM_001300860.2(DDX46):c.661G>A (p.Glu221Lys)	not specified [RCV004908794]	uncertain significance	5	134777621	134777621	Human		name
152981170	CV1676429	single nucleotide variant	NM_001300860.2(DDX46):c.2819A>G (p.Asn940Ser)	See cases [RCV005255494]	uncertain significance	5	134817701	134817701	Human		name
156160303	CV2323356	single nucleotide variant	NM_001300860.2(DDX46):c.1810A>G (p.Lys604Glu)	not specified [RCV004171760]	uncertain significance	5	134796006	134796006	Human		name
329376892	CV2460630	single nucleotide variant	NM_001300860.2(DDX46):c.2266T>A (p.Phe756Ile)	not specified [RCV004268896]	uncertain significance	5	134811338	134811338	Human		name
401732893	CV2691142	single nucleotide variant	NM_001300860.2(DDX46):c.1063T>A (p.Leu355Met)	not specified [RCV004301136]	uncertain significance	5	134782962	134782962	Human		name
401885991	CV2770999	single nucleotide variant	NM_001300860.2(DDX46):c.1852G>C (p.Glu618Gln)	not specified [RCV004344016]	uncertain significance	5	134796048	134796048	Human		name
405705439	CV3239899	single nucleotide variant	NM_001300860.2(DDX46):c.1634G>A (p.Arg545His)	not specified [RCV004375846]	uncertain significance	5	134794857	134794857	Human		name
405705444	CV3239900	single nucleotide variant	NM_001300860.2(DDX46):c.1816T>C (p.Phe606Leu)	not specified [RCV004375847]	uncertain significance	5	134796012	134796012	Human		name
405705451	CV3239901	single nucleotide variant	NM_001300860.2(DDX46):c.2260A>C (p.Ser754Arg)	not specified [RCV004375848]	uncertain significance	5	134811332	134811332	Human		name
598222626	CV3956353	single nucleotide variant	NM_001300860.2(DDX46):c.2620A>G (p.Met874Val)	not specified [RCV005317946]	uncertain significance	5	134817502	134817502	Human		name
598222633	CV3956354	single nucleotide variant	NM_001300860.2(DDX46):c.2093A>G (p.Asn698Ser)	not specified [RCV005317947]	uncertain significance	5	134807886	134807886	Human		name
598222639	CV3956355	single nucleotide variant	NM_001300860.2(DDX46):c.1303A>G (p.Met435Val)	not specified [RCV005317948]	uncertain significance	5	134784502	134784502	Human		name