Asb11 Variant Search Result - Rat Genome Database

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36 records found for search term Asb11

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401931068	CV2823916	single nucleotide variant	NM_080873.3(ASB11):c.847+6C>A	not provided [RCV003441034]	likely benign	X	15287875	15287875	Human		name
405675183	CV3286696	single nucleotide variant	NM_080873.3(ASB11):c.14C>T (p.Pro5Leu)	not specified [RCV004420504]	uncertain significance	X	15315592	15315592	Human		name
156021778	CV2264494	single nucleotide variant	NM_080873.3(ASB11):c.59C>T (p.Thr20Met)	not specified [RCV004138386]	uncertain significance	X	15315547	15315547	Human		name
329388142	CV2437122	single nucleotide variant	NM_080873.3(ASB11):c.42T>G (p.Phe14Leu)	not specified [RCV004262929]	uncertain significance	X	15315564	15315564	Human		name
401931070	CV2823917	single nucleotide variant	NM_080873.3(ASB11):c.684G>A (p.Leu228=)	not provided [RCV003441035]	likely benign	X	15288044	15288044	Human		name
405675187	CV3286697	single nucleotide variant	NM_080873.3(ASB11):c.40T>C (p.Phe14Leu)	not specified [RCV004420505]	uncertain significance	X	15315566	15315566	Human		name
41407376	CV982285	single nucleotide variant	NM_080873.3(ASB11):c.306C>G (p.Leu102=)	not provided [RCV001810676]	uncertain significance	X	15297637	15297637	Human		name
156001276	CV2296394	single nucleotide variant	NM_080873.3(ASB11):c.116A>G (p.Tyr39Cys)	not specified [RCV004148142]	uncertain significance	X	15315490	15315490	Human		name
405675179	CV3286695	single nucleotide variant	NM_080873.3(ASB11):c.121G>A (p.Val41Ile)	not specified [RCV004420503]	uncertain significance	X	15315485	15315485	Human		name
598215563	CV3905548	single nucleotide variant	NM_080873.3(ASB11):c.202C>T (p.Pro68Ser)	not specified [RCV005271721]	uncertain significance	X	15302787	15302787	Human		name
155959679	CV2193981	single nucleotide variant	NM_080873.3(ASB11):c.874C>T (p.Arg292Cys)	not specified [RCV004074706]	uncertain significance	X	15283603	15283603	Human		name
155919923	CV2209785	single nucleotide variant	NM_080873.3(ASB11):c.886C>T (p.Arg296Trp)	not specified [RCV004076257]	uncertain significance	X	15283591	15283591	Human		name
155940019	CV2221920	single nucleotide variant	NM_080873.3(ASB11):c.341C>G (p.Ala114Gly)	not specified [RCV004102932]	uncertain significance	X	15297602	15297602	Human		name
156153826	CV2242177	single nucleotide variant	NM_080873.3(ASB11):c.379G>A (p.Val127Met)	not specified [RCV004109390]	uncertain significance	X	15293311	15293311	Human		name
156210203	CV2259790	single nucleotide variant	NM_080873.3(ASB11):c.460G>A (p.Gly154Arg)	not specified [RCV004117066]	uncertain significance	X	15293230	15293230	Human		name
156243393	CV2306768	single nucleotide variant	NM_080873.3(ASB11):c.803C>T (p.Ala268Val)	not specified [RCV004159347]	uncertain significance	X	15287925	15287925	Human		name
156290897	CV2324949	single nucleotide variant	NM_080873.3(ASB11):c.688A>T (p.Thr230Ser)	not specified [RCV004175205]	uncertain significance	X	15288040	15288040	Human		name
156120414	CV2354164	single nucleotide variant	NM_080873.3(ASB11):c.767G>A (p.Arg256His)	not provided [RCV004695659]\|not specified [RCV004206598]	uncertain significance	X	15287961	15287961	Human		name
329374496	CV2443754	single nucleotide variant	NM_080873.3(ASB11):c.965A>G (p.Tyr322Cys)	not specified [RCV004256053]	uncertain significance	X	15283512	15283512	Human		name
329401933	CV2457999	single nucleotide variant	NM_080873.3(ASB11):c.841C>T (p.Arg281Cys)	not specified [RCV004271573]	uncertain significance	X	15287887	15287887	Human		name
401931071	CV2823918	single nucleotide variant	NM_080873.3(ASB11):c.494C>T (p.Ser165Leu)	not provided [RCV003441036]	likely benign	X	15293196	15293196	Human		name
405675461	CV3286698	single nucleotide variant	NM_080873.3(ASB11):c.589G>A (p.Gly197Arg)	not specified [RCV004420506]	uncertain significance	X	15289570	15289570	Human		name
405675194	CV3286699	single nucleotide variant	NM_080873.3(ASB11):c.767G>T (p.Arg256Leu)	not specified [RCV004420507]	likely benign	X	15287961	15287961	Human		name
405675199	CV3286700	single nucleotide variant	NM_080873.3(ASB11):c.820G>A (p.Val274Met)	not specified [RCV004420508]	uncertain significance	X	15287908	15287908	Human		name
407492193	CV3476803	single nucleotide variant	NM_080873.3(ASB11):c.488T>C (p.Leu163Pro)	not specified [RCV004667050]	uncertain significance	X	15293202	15293202	Human		name
597686405	CV3593998	single nucleotide variant	NM_080873.3(ASB11):c.433G>A (p.Ala145Thr)	not specified [RCV004858380]	uncertain significance	X	15293257	15293257	Human		name
597686495	CV3594022	single nucleotide variant	NM_080873.3(ASB11):c.875G>T (p.Arg292Leu)	not specified [RCV004858390]	uncertain significance	X	15283602	15283602	Human		name
597686545	CV3594032	single nucleotide variant	NM_080873.3(ASB11):c.868C>T (p.Leu290Phe)	not specified [RCV004858395]	uncertain significance	X	15283609	15283609	Human		name
598215546	CV3905544	single nucleotide variant	NM_080873.3(ASB11):c.529G>A (p.Glu177Lys)	not specified [RCV005271717]	uncertain significance	X	15289630	15289630	Human		name
598215573	CV3905550	single nucleotide variant	NM_080873.3(ASB11):c.958C>T (p.Leu320Phe)	not specified [RCV005271723]	uncertain significance	X	15283519	15283519	Human		name
598215580	CV3905551	single nucleotide variant	NM_080873.3(ASB11):c.443A>T (p.Asn148Ile)	not specified [RCV005271724]	uncertain significance	X	15293247	15293247	Human		name
598215601	CV3905555	single nucleotide variant	NM_080873.3(ASB11):c.776C>G (p.Ala259Gly)	not specified [RCV005271728]	uncertain significance	X	15287952	15287952	Human		name
15181205	CV717693	single nucleotide variant	NM_080873.3(ASB11):c.745G>A (p.Asp249Asn)	not provided [RCV000974335]	benign	X	15287983	15287983	Human		name
15130471	CV717694	single nucleotide variant	NM_080873.3(ASB11):c.622A>T (p.Arg208Trp)	not provided [RCV000964441]	benign	X	15289537	15289537	Human		name
39457121	CV965871	single nucleotide variant	NM_080873.3(ASB11):c.871T>C (p.Cys291Arg)	not specified [RCV001255481]	uncertain significance	X	15283606	15283606	Human		name
150411055	CV1196331	deletion	NM_080873.3(ASB11):c.287_290del (p.Ile96fs)	not provided [RCV001573458]	uncertain significance	X	15297653	15297656	Human		name

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