P2ry10 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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17 records found for search term P2ry10

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8587621	CV122252	single nucleotide variant	NM_198333.1(P2RY10):c.-13-3532T>A	Lung cancer [RCV000102772]	uncertain significance	X	78956976	78956976	Human		name
156284660	CV2360681	single nucleotide variant	NM_014499.4(P2RY10):c.88G>C (p.Val30Leu)	not specified [RCV004213476]	uncertain significance	X	78960608	78960608	Human		name
401929049	CV2826563	single nucleotide variant	NM_014499.4(P2RY10):c.420G>A (p.Arg140=)	not provided [RCV003439702]	likely benign	X	78960940	78960940	Human		name
405739510	CV3371269	single nucleotide variant	NM_014499.4(P2RY10):c.53C>A (p.Thr18Asn)	not specified [RCV004497518]	uncertain significance	X	78960573	78960573	Human		name
407517384	CV3469968	single nucleotide variant	NM_014499.4(P2RY10):c.52A>G (p.Thr18Ala)	not specified [RCV004650627]	uncertain significance	X	78960572	78960572	Human		name
15120899	CV717869	single nucleotide variant	NM_014499.4(P2RY10):c.396C>T (p.Cys132=)	not provided [RCV000962796]	benign	X	78960916	78960916	Human		name
597693269	CV3578144	single nucleotide variant	NM_014499.4(P2RY10):c.268C>T (p.Arg90Trp)	not specified [RCV004838892]	uncertain significance	X	78960788	78960788	Human		name
156375403	CV2210165	single nucleotide variant	NM_014499.4(P2RY10):c.310G>A (p.Ala104Thr)	not specified [RCV004087554]	uncertain significance	X	78960830	78960830	Human		name
156017962	CV2223039	single nucleotide variant	NM_014499.4(P2RY10):c.790A>G (p.Ile264Val)	not specified [RCV004103620]	uncertain significance	X	78961310	78961310	Human		name
156026748	CV2242385	single nucleotide variant	NM_014499.4(P2RY10):c.475G>T (p.Val159Phe)	not specified [RCV004111387]	uncertain significance	X	78960995	78960995	Human		name
156064075	CV2389444	single nucleotide variant	NM_014499.4(P2RY10):c.530A>G (p.Asn177Ser)	not specified [RCV004238170]	uncertain significance	X	78961050	78961050	Human		name
405739518	CV3371270	single nucleotide variant	NM_014499.4(P2RY10):c.910C>T (p.Leu304Phe)	not specified [RCV004497519]	uncertain significance	X	78961430	78961430	Human		name
407517386	CV3469969	single nucleotide variant	NM_014499.4(P2RY10):c.350T>C (p.Met117Thr)	not specified [RCV004650628]	uncertain significance	X	78960870	78960870	Human		name
407478668	CV3469970	single nucleotide variant	NM_014499.4(P2RY10):c.448G>C (p.Val150Leu)	not specified [RCV004663955]	uncertain significance	X	78960968	78960968	Human		name
597693281	CV3578145	single nucleotide variant	NM_014499.4(P2RY10):c.749C>T (p.Ala250Val)	not specified [RCV004838893]	uncertain significance	X	78961269	78961269	Human		name
597656831	CV3578146	single nucleotide variant	NM_014499.4(P2RY10):c.643G>T (p.Ala215Ser)	not specified [RCV004827542]	uncertain significance	X	78961163	78961163	Human		name
598163359	CV3995850	single nucleotide variant	NM_014499.4(P2RY10):c.703A>T (p.Ile235Phe)	not specified [RCV005390973]	uncertain significance	X	78961223	78961223	Human		name