Arrdc5 Variant Search Result - Rat Genome Database

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42 records found for search term Arrdc5

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405664342	CV3290438	single nucleotide variant	NM_001080523.3(ARRDC5):c.-24T>C	not specified [RCV004418211]	uncertain significance	19	4902849	4902849	Human		name
597731209	CV3593345	single nucleotide variant	NM_001080523.3(ARRDC5):c.-15A>T	not specified [RCV004863108]	uncertain significance	19	4902840	4902840	Human		name
401936098	CV2815250	single nucleotide variant	NM_001080523.3(ARRDC5):c.150C>T (p.Val50=)	not provided [RCV003413541]	likely benign	19	4902676	4902676	Human		name
405664741	CV3286479	single nucleotide variant	NM_001080523.3(ARRDC5):c.37G>A (p.Glu13Lys)	not specified [RCV004418217]	likely benign	19	4902789	4902789	Human		name
597731168	CV3593325	single nucleotide variant	NM_001080523.3(ARRDC5):c.31C>A (p.Leu11Met)	not specified [RCV004863104]	uncertain significance	19	4902795	4902795	Human		name
597765290	CV3593364	single nucleotide variant	NM_001080523.3(ARRDC5):c.34C>G (p.Pro12Ala)	not specified [RCV004849997]	uncertain significance	19	4902792	4902792	Human		name
8636866	CV92091	single nucleotide variant	NM_001080523.1(ARRDC5):c.912C>T (p.Ser304=)	Malignant melanoma [RCV000072189]	not provided	19	4891163	4891163	Human		name
156144617	CV2200175	single nucleotide variant	NM_001080523.3(ARRDC5):c.254A>G (p.Asp85Gly)	not specified [RCV004069742]	uncertain significance	19	4896876	4896876	Human		name
155995504	CV2375823	single nucleotide variant	NM_001080523.3(ARRDC5):c.268G>T (p.Ala90Ser)	not specified [RCV004224403]	uncertain significance	19	4896862	4896862	Human		name
401720512	CV2673355	single nucleotide variant	NM_001080523.3(ARRDC5):c.151G>A (p.Glu51Lys)	not specified [RCV004288338]	uncertain significance	19	4902675	4902675	Human		name
401862608	CV2775249	single nucleotide variant	NM_001080523.3(ARRDC5):c.119T>G (p.Val40Gly)	not specified [RCV004348375]	uncertain significance	19	4902707	4902707	Human		name
405664336	CV3290437	single nucleotide variant	NM_001080523.3(ARRDC5):c.111C>A (p.Asp37Glu)	not specified [RCV004418210]	uncertain significance	19	4902715	4902715	Human		name
405664346	CV3290439	single nucleotide variant	NM_001080523.3(ARRDC5):c.220T>C (p.Tyr74His)	not specified [RCV004418212]	uncertain significance	19	4902606	4902606	Human		name
597765238	CV3593317	single nucleotide variant	NM_001080523.3(ARRDC5):c.127G>A (p.Glu43Lys)	not specified [RCV004849983]	uncertain significance	19	4902699	4902699	Human		name
156340786	CV2225684	single nucleotide variant	NM_001080523.3(ARRDC5):c.790T>G (p.Ser264Ala)	not specified [RCV004103107]	uncertain significance	19	4891243	4891243	Human		name
156146780	CV2265156	single nucleotide variant	NM_001080523.3(ARRDC5):c.830C>A (p.Thr277Asn)	not specified [RCV004126284]	uncertain significance	19	4891203	4891203	Human		name
156086107	CV2289908	single nucleotide variant	NM_001080523.3(ARRDC5):c.910A>G (p.Ser304Gly)	not specified [RCV004150564]	uncertain significance	19	4891123	4891123	Human		name
156282176	CV2363103	single nucleotide variant	NM_001080523.3(ARRDC5):c.584C>G (p.Thr195Arg)	not specified [RCV004211228]	uncertain significance	19	4891449	4891449	Human		name
156187280	CV2378056	single nucleotide variant	NM_001080523.3(ARRDC5):c.665C>T (p.Thr222Met)	not specified [RCV004232617]	uncertain significance	19	4891368	4891368	Human		name
156210091	CV2382714	single nucleotide variant	NM_001080523.3(ARRDC5):c.908C>T (p.Thr303Ile)	not specified [RCV004233023]	uncertain significance	19	4891125	4891125	Human		name
156000933	CV2383293	single nucleotide variant	NM_001080523.3(ARRDC5):c.617A>G (p.Lys206Arg)	not specified [RCV004222340]	uncertain significance	19	4891416	4891416	Human		name
156057544	CV2396361	single nucleotide variant	NM_001080523.3(ARRDC5):c.722C>T (p.Ala241Val)	not specified [RCV004242085]	uncertain significance	19	4891311	4891311	Human		name
329391668	CV2453021	single nucleotide variant	NM_001080523.3(ARRDC5):c.659G>A (p.Gly220Asp)	not specified [RCV004277640]	uncertain significance	19	4891374	4891374	Human		name
401728439	CV2672931	single nucleotide variant	NM_001080523.3(ARRDC5):c.620C>T (p.Thr207Met)	not specified [RCV004283934]	uncertain significance	19	4891413	4891413	Human		name
401721423	CV2673710	single nucleotide variant	NM_001080523.3(ARRDC5):c.591C>G (p.Ile197Met)	not specified [RCV004282438]	uncertain significance	19	4891442	4891442	Human		name
401739115	CV2676439	single nucleotide variant	NM_001080523.3(ARRDC5):c.602C>T (p.Thr201Ile)	not specified [RCV004286455]	uncertain significance	19	4891431	4891431	Human		name
401754439	CV2685269	single nucleotide variant	NM_001080523.3(ARRDC5):c.329C>T (p.Thr110Ile)	not specified [RCV004289813]	uncertain significance	19	4896801	4896801	Human		name
401734420	CV2690584	single nucleotide variant	NM_001080523.3(ARRDC5):c.403A>G (p.Arg135Gly)	not specified [RCV004304679]	uncertain significance	19	4896727	4896727	Human		name
401858252	CV2774253	single nucleotide variant	NM_001080523.3(ARRDC5):c.540G>A (p.Met180Ile)	not specified [RCV004347621]	uncertain significance	19	4891493	4891493	Human		name
405664365	CV3286478	single nucleotide variant	NM_001080523.3(ARRDC5):c.655G>A (p.Glu219Lys)	not specified [RCV004418216]	uncertain significance	19	4891378	4891378	Human		name
405664376	CV3286480	single nucleotide variant	NM_001080523.3(ARRDC5):c.822C>G (p.Ile274Met)	not specified [RCV004418218]	uncertain significance	19	4891211	4891211	Human		name
405664351	CV3290440	single nucleotide variant	NM_001080523.3(ARRDC5):c.376G>T (p.Gly126Cys)	not specified [RCV004418213]	uncertain significance	19	4896754	4896754	Human		name
405664357	CV3290441	single nucleotide variant	NM_001080523.3(ARRDC5):c.387C>G (p.His129Gln)	not specified [RCV004418214]	uncertain significance	19	4896743	4896743	Human		name
405664360	CV3290442	single nucleotide variant	NM_001080523.3(ARRDC5):c.503G>T (p.Cys168Phe)	not specified [RCV004418215]	uncertain significance	19	4891530	4891530	Human		name
407514428	CV3483884	single nucleotide variant	NM_001080523.3(ARRDC5):c.862C>G (p.Pro288Ala)	not specified [RCV004674543]	uncertain significance	19	4891171	4891171	Human		name
407514430	CV3483892	single nucleotide variant	NM_001080523.3(ARRDC5):c.733G>C (p.Val245Leu)	not specified [RCV004674544]	uncertain significance	19	4891300	4891300	Human		name
597765242	CV3593334	single nucleotide variant	NM_001080523.3(ARRDC5):c.648A>G (p.Ile216Met)	not specified [RCV004849984]	uncertain significance	19	4891385	4891385	Human		name
597765272	CV3593354	single nucleotide variant	NM_001080523.3(ARRDC5):c.775C>A (p.Leu259Met)	not specified [RCV004849992]	uncertain significance	19	4891258	4891258	Human		name
598185678	CV3902359	single nucleotide variant	NM_001080523.3(ARRDC5):c.649C>A (p.Gln217Lys)	not specified [RCV005265956]	uncertain significance	19	4891384	4891384	Human		name
598185768	CV3902377	single nucleotide variant	NM_001080523.3(ARRDC5):c.733G>A (p.Val245Met)	not specified [RCV005265974]	likely benign	19	4891300	4891300	Human		name
598185809	CV3902385	single nucleotide variant	NM_001080523.3(ARRDC5):c.973G>A (p.Asp325Asn)	not specified [RCV005265982]	uncertain significance	19	4891060	4891060	Human		name
598185848	CV3902392	single nucleotide variant	NM_001080523.3(ARRDC5):c.341G>A (p.Gly114Asp)	not specified [RCV005265989]	uncertain significance	19	4896789	4896789	Human		name

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