Synpr Variant Search Result - Rat Genome Database

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26 records found for search term Synpr

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
597780309	CV3618906	single nucleotide variant	NM_001130003.2(SYNPR):c.19C>T (p.Leu7=)	not specified [RCV004873775]	likely benign	3	63278677	63278677	Human		name
598264118	CV3923414	single nucleotide variant	NM_001130003.2(SYNPR):c.22G>A (p.Ala8Thr)	not specified [RCV005280707]	uncertain significance	3	63278680	63278680	Human		name
401746661	CV2678890	single nucleotide variant	NM_001130003.2(SYNPR):c.40C>T (p.Arg14Trp)	not specified [RCV004292863]	uncertain significance	3	63278698	63278698	Human		name
401743254	CV2684657	single nucleotide variant	NM_001130003.2(SYNPR):c.44T>A (p.Val15Glu)	not specified [RCV004293754]	uncertain significance	3	63278702	63278702	Human		name
401873042	CV2793189	single nucleotide variant	NM_001130003.2(SYNPR):c.71G>A (p.Arg24Gln)	not specified [RCV004360494]	uncertain significance	3	63278729	63278729	Human		name
156064424	CV2200174	single nucleotide variant	NM_001130003.2(SYNPR):c.154G>A (p.Val52Ile)	not specified [RCV004069741]	uncertain significance	3	63480901	63480901	Human		name
155962187	CV2200897	single nucleotide variant	NM_001130003.2(SYNPR):c.115G>A (p.Gly39Ser)	not specified [RCV004081516]	uncertain significance	3	63480862	63480862	Human		name
156065478	CV2348822	single nucleotide variant	NM_001130003.2(SYNPR):c.200A>G (p.Tyr67Cys)	not specified [RCV004203266]	uncertain significance	3	63480947	63480947	Human		name
405726515	CV3334784	single nucleotide variant	NM_001130003.2(SYNPR):c.107C>T (p.Ala36Val)	not specified [RCV004463824]	uncertain significance	3	63480854	63480854	Human		name
597780304	CV3618905	single nucleotide variant	NM_001130003.2(SYNPR):c.172A>G (p.Asn58Asp)	not specified [RCV004873774]	uncertain significance	3	63480919	63480919	Human		name
155988843	CV2234255	single nucleotide variant	NM_001130003.2(SYNPR):c.392A>C (p.Asn131Thr)	not specified [RCV004106328]	uncertain significance	3	63556725	63556725	Human		name
155983728	CV2275209	single nucleotide variant	NM_001130003.2(SYNPR):c.335A>G (p.Tyr112Cys)	not specified [RCV004137000]	uncertain significance	3	63556668	63556668	Human		name
156069822	CV2292833	single nucleotide variant	NM_001130003.2(SYNPR):c.307G>A (p.Val103Ile)	not specified [RCV004148350]	uncertain significance	3	63556640	63556640	Human		name
156047439	CV2319164	single nucleotide variant	NM_001130003.2(SYNPR):c.700C>T (p.Pro234Ser)	not specified [RCV004178229]	uncertain significance	3	63615323	63615323	Human		name
329368793	CV2450419	single nucleotide variant	NM_001130003.2(SYNPR):c.625C>G (p.Leu209Val)	not specified [RCV004265347]	uncertain significance	3	63615248	63615248	Human		name
401768796	CV2735433	single nucleotide variant	NM_001130003.2(SYNPR):c.664G>A (p.Gly222Ser)	not specified [RCV004330995]	uncertain significance	3	63615287	63615287	Human		name
405726533	CV3334786	single nucleotide variant	NM_001130003.2(SYNPR):c.383G>A (p.Arg128Gln)	not specified [RCV004463826]	uncertain significance	3	63556716	63556716	Human		name
405726539	CV3334787	single nucleotide variant	NM_001130003.2(SYNPR):c.499G>T (p.Asp167Tyr)	not specified [RCV004463827]	uncertain significance	3	63609215	63609215	Human		name
405726557	CV3334789	single nucleotide variant	NM_001130003.2(SYNPR):c.673T>G (p.Ser225Ala)	not specified [RCV004463829]	uncertain significance	3	63615296	63615296	Human		name
405726563	CV3334790	single nucleotide variant	NM_001130003.2(SYNPR):c.805G>T (p.Asp269Tyr)	not specified [RCV004463830]	uncertain significance	3	63615428	63615428	Human		name
407505767	CV3478328	single nucleotide variant	NM_001130003.2(SYNPR):c.677C>T (p.Ser226Leu)	not specified [RCV004670928]	uncertain significance	3	63615300	63615300	Human		name
407530329	CV3478329	single nucleotide variant	NM_001130003.2(SYNPR):c.758G>T (p.Gly253Val)	not specified [RCV004681855]	uncertain significance	3	63615381	63615381	Human		name
597780312	CV3618907	single nucleotide variant	NM_001130003.2(SYNPR):c.745C>A (p.Gln249Lys)	not specified [RCV004873776]	uncertain significance	3	63615368	63615368	Human		name
597780316	CV3618908	single nucleotide variant	NM_001130003.2(SYNPR):c.557T>C (p.Met186Thr)	not specified [RCV004873777]	uncertain significance	3	63609273	63609273	Human		name
597780319	CV3618909	single nucleotide variant	NM_001130003.2(SYNPR):c.670C>T (p.His224Tyr)	not specified [RCV004873778]	uncertain significance	3	63615293	63615293	Human		name
597780323	CV3618910	single nucleotide variant	NM_001130003.2(SYNPR):c.352G>A (p.Val118Ile)	not specified [RCV004873779]	uncertain significance	3	63556685	63556685	Human		name

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