Scai Variant Search Result - Rat Genome Database

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8651105	CV127680	single nucleotide variant	NM_173690.4(SCAI):c.930+297A>G	Lung cancer [RCV000108167]	uncertain significance	9	125018502	125018502	Human		name
8633236	CV88449	single nucleotide variant	NM_173690.4(SCAI):c.1815G>A (p.Gln605=)	Malignant melanoma [RCV000068541]	not provided	9	124952882	124952882	Human		name
8633237	CV88450	single nucleotide variant	NM_173690.4(SCAI):c.1467A>G (p.Gln489=)	Malignant melanoma [RCV000068542]	not provided	9	124976115	124976115	Human		name
405742435	CV3317068	single nucleotide variant	NM_001144877.3(SCAI):c.231A>G (p.Arg77=)	not specified [RCV004452588]	likely benign	9	125029739	125029739	Human		name
405742447	CV3317070	single nucleotide variant	NM_001144877.3(SCAI):c.74A>G (p.Lys25Arg)	not specified [RCV004452590]	uncertain significance	9	125142657	125142657	Human		name
597669889	CV3601585	single nucleotide variant	NM_001144877.3(SCAI):c.47C>T (p.Ala16Val)	not specified [RCV004856220]	uncertain significance	9	125143391	125143391	Human		name
156335864	CV2273047	single nucleotide variant	NM_001144877.3(SCAI):c.221A>G (p.Asn74Ser)	not specified [RCV004137699]	uncertain significance	9	125055885	125055885	Human		name
407514405	CV3483833	single nucleotide variant	NM_001144877.3(SCAI):c.128C>A (p.Ser43Tyr)	not specified [RCV004674530]	uncertain significance	9	125055978	125055978	Human		name
156186239	CV2346590	single nucleotide variant	NM_001144877.3(SCAI):c.644G>A (p.Arg215Gln)	not specified [RCV004206500]	uncertain significance	9	125019171	125019171	Human		name
329378926	CV2460044	single nucleotide variant	NM_001144877.3(SCAI):c.522G>T (p.Leu174Phe)	not specified [RCV004273169]	uncertain significance	9	125020760	125020760	Human		name
329388100	CV2468694	single nucleotide variant	NM_001144877.3(SCAI):c.904C>G (p.Gln302Glu)	not specified [RCV004280024]	uncertain significance	9	125003528	125003528	Human		name
401773495	CV2716591	single nucleotide variant	NM_001144877.3(SCAI):c.831C>G (p.Asp277Glu)	not specified [RCV004327664]	uncertain significance	9	125018829	125018829	Human		name
401896439	CV2781367	single nucleotide variant	NM_001144877.3(SCAI):c.945G>C (p.Met315Ile)	not specified [RCV004352375]	uncertain significance	9	125003487	125003487	Human		name
405742441	CV3317069	single nucleotide variant	NM_001144877.3(SCAI):c.344G>T (p.Arg115Leu)	not specified [RCV004452589]	uncertain significance	9	125028461	125028461	Human		name
405742457	CV3317071	single nucleotide variant	NM_001144877.3(SCAI):c.838A>G (p.Ile280Val)	not specified [RCV004452591]	uncertain significance	9	125018822	125018822	Human		name
597669834	CV3601578	single nucleotide variant	NM_001144877.3(SCAI):c.638C>G (p.Thr213Ser)	not specified [RCV004856213]	uncertain significance	9	125019177	125019177	Human		name
597669852	CV3601580	single nucleotide variant	NM_001144877.3(SCAI):c.781G>T (p.Ala261Ser)	not specified [RCV004856215]	uncertain significance	9	125018879	125018879	Human		name
597669859	CV3601581	single nucleotide variant	NM_001144877.3(SCAI):c.541T>C (p.Tyr181His)	not specified [RCV004856216]	uncertain significance	9	125020741	125020741	Human		name
597669868	CV3601582	single nucleotide variant	NM_001144877.3(SCAI):c.350G>A (p.Gly117Asp)	not specified [RCV004856217]	uncertain significance	9	125028455	125028455	Human		name
597669874	CV3601583	single nucleotide variant	NM_001144877.3(SCAI):c.827C>A (p.Ala276Asp)	not specified [RCV004856218]	uncertain significance	9	125018833	125018833	Human		name
598195937	CV3900227	single nucleotide variant	NM_001144877.3(SCAI):c.993A>C (p.Glu331Asp)	not specified [RCV005267848]	uncertain significance	9	125003186	125003186	Human		name
598195952	CV3900230	single nucleotide variant	NM_001144877.3(SCAI):c.597G>C (p.Lys199Asn)	not specified [RCV005267851]	uncertain significance	9	125020685	125020685	Human		name
156296456	CV2236565	single nucleotide variant	NM_001144877.3(SCAI):c.1591T>C (p.Phe531Leu)	not specified [RCV004110558]	uncertain significance	9	124971453	124971453	Human		name
155999069	CV2261052	single nucleotide variant	NM_001144877.3(SCAI):c.1079A>G (p.Asn360Ser)	not specified [RCV004127704]	uncertain significance	9	125002030	125002030	Human		name
155976335	CV2324674	single nucleotide variant	NM_001144877.3(SCAI):c.1328A>G (p.Asn443Ser)	not specified [RCV004172918]	uncertain significance	9	124976185	124976185	Human		name
155922203	CV2340583	single nucleotide variant	NM_001144877.3(SCAI):c.1535G>A (p.Arg512His)	not specified [RCV004197291]	uncertain significance	9	124971709	124971709	Human		name
156275887	CV2351878	single nucleotide variant	NM_001144877.3(SCAI):c.1738C>A (p.His580Asn)	not specified [RCV004198021]	uncertain significance	9	124952890	124952890	Human		name
156341519	CV2368419	single nucleotide variant	NM_001144877.3(SCAI):c.1633A>G (p.Ile545Val)	not specified [RCV004219186]	uncertain significance	9	124971411	124971411	Human		name
156263274	CV2368635	single nucleotide variant	NM_001144877.3(SCAI):c.1130G>A (p.Arg377His)	not specified [RCV004221411]	uncertain significance	9	125001979	125001979	Human		name
401766696	CV2680119	single nucleotide variant	NM_001144877.3(SCAI):c.1750C>A (p.His584Asn)	not specified [RCV004286607]	uncertain significance	9	124952878	124952878	Human		name
401728455	CV2731735	single nucleotide variant	NM_001144877.3(SCAI):c.1565G>A (p.Arg522His)	not specified [RCV004331834]	uncertain significance	9	124971679	124971679	Human		name
405742427	CV3317067	single nucleotide variant	NM_001144877.3(SCAI):c.1429C>T (p.Leu477Phe)	not specified [RCV004452587]	uncertain significance	9	124971815	124971815	Human		name
407461090	CV3483834	single nucleotide variant	NM_001144877.3(SCAI):c.1558C>T (p.His520Tyr)	not specified [RCV004658622]	uncertain significance	9	124971686	124971686	Human		name
407461093	CV3483835	single nucleotide variant	NM_001144877.3(SCAI):c.1451T>C (p.Met484Thr)	not specified [RCV004658623]	uncertain significance	9	124971793	124971793	Human		name
597669826	CV3601577	single nucleotide variant	NM_001144877.3(SCAI):c.1412G>A (p.Arg471Gln)	not specified [RCV004856212]	uncertain significance	9	124971832	124971832	Human		name
597669882	CV3601584	single nucleotide variant	NM_001144877.3(SCAI):c.1738C>T (p.His580Tyr)	not specified [RCV004856219]	uncertain significance	9	124952890	124952890	Human		name
598195942	CV3900228	single nucleotide variant	NM_001144877.3(SCAI):c.1318G>T (p.Ala440Ser)	not specified [RCV005267849]	uncertain significance	9	124994942	124994942	Human		name
598195947	CV3900229	single nucleotide variant	NM_001144877.3(SCAI):c.1217G>A (p.Arg406Gln)	not specified [RCV005267850]	uncertain significance	9	124999918	124999918	Human		name
598195958	CV3900231	single nucleotide variant	NM_001144877.3(SCAI):c.1177A>G (p.Ser393Gly)	not specified [RCV005267852]	uncertain significance	9	124999958	124999958	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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InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

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

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