Ccdc159 Variant Search Result - Rat Genome Database

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34 records found for search term Ccdc159

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156306955	CV2252794	single nucleotide variant	NM_001080503.3(CCDC159):c.254G>A (p.Gly85Glu)	not specified [RCV004118633]	uncertain significance	19	11350835	11350835	Human		name
155905705	CV2283141	single nucleotide variant	NM_001080503.3(CCDC159):c.175A>T (p.Met59Leu)	not specified [RCV004145828]	uncertain significance	19	11350148	11350148	Human		name
156102803	CV2352318	single nucleotide variant	NM_001080503.3(CCDC159):c.134C>A (p.Ala45Asp)	not specified [RCV004200792]	uncertain significance	19	11350016	11350016	Human		name
156181603	CV2353095	single nucleotide variant	NM_001080503.3(CCDC159):c.292C>T (p.Arg98Trp)	not specified [RCV004203577]	uncertain significance	19	11350873	11350873	Human		name
329365420	CV2444856	single nucleotide variant	NM_001080503.3(CCDC159):c.247C>T (p.Arg83Cys)	not specified [RCV004259094]	uncertain significance	19	11350828	11350828	Human		name
329385701	CV2462219	single nucleotide variant	NM_001080503.3(CCDC159):c.170T>G (p.Val57Gly)	not specified [RCV004266225]	uncertain significance	19	11350143	11350143	Human		name
401771197	CV2700923	single nucleotide variant	NM_001080503.3(CCDC159):c.242C>T (p.Thr81Ile)	not specified [RCV004307188]	uncertain significance	19	11350823	11350823	Human		name
405769080	CV3303122	single nucleotide variant	NM_001080503.3(CCDC159):c.248G>A (p.Arg83His)	not specified [RCV004434965]	uncertain significance	19	11350829	11350829	Human		name
407484191	CV3418381	single nucleotide variant	NM_001080503.3(CCDC159):c.272A>G (p.Lys91Arg)	not specified [RCV004602967]	uncertain significance	19	11350853	11350853	Human		name
597787237	CV3647842	single nucleotide variant	NM_001080503.3(CCDC159):c.293G>C (p.Arg98Pro)	not specified [RCV004901179]	uncertain significance	19	11350874	11350874	Human		name
156070423	CV2204000	single nucleotide variant	NM_001080503.3(CCDC159):c.703G>A (p.Val235Met)	not specified [RCV004070041]	uncertain significance	19	11353805	11353805	Human		name
156129218	CV2209727	single nucleotide variant	NM_001080503.3(CCDC159):c.349C>T (p.Arg117Cys)	not specified [RCV004083049]	uncertain significance	19	11350930	11350930	Human		name
156375232	CV2213536	single nucleotide variant	NM_001080503.3(CCDC159):c.376C>G (p.Arg126Gly)	not specified [RCV004087495]	uncertain significance	19	11350957	11350957	Human		name
156348728	CV2379657	single nucleotide variant	NM_001080503.3(CCDC159):c.829G>A (p.Asp277Asn)	not specified [RCV004219784]	uncertain significance	19	11354636	11354636	Human		name
155968737	CV2391492	single nucleotide variant	NM_001080503.3(CCDC159):c.748T>C (p.Cys250Arg)	not specified [RCV004239878]	likely benign	19	11353850	11353850	Human		name
329385536	CV2462004	single nucleotide variant	NM_001080503.3(CCDC159):c.715T>G (p.Ser239Ala)	not specified [RCV004272187]	uncertain significance	19	11353817	11353817	Human		name
329380447	CV2466626	single nucleotide variant	NM_001080503.3(CCDC159):c.823G>A (p.Asp275Asn)	not specified [RCV004274149]	uncertain significance	19	11354630	11354630	Human		name
401738769	CV2676368	single nucleotide variant	NM_001080503.3(CCDC159):c.566A>G (p.Lys189Arg)	not specified [RCV004286394]	uncertain significance	19	11352132	11352132	Human		name
401757388	CV2734990	single nucleotide variant	NM_001080503.3(CCDC159):c.458G>A (p.Arg153Gln)	not specified [RCV004333694]	uncertain significance	19	11351941	11351941	Human		name
405769086	CV3303123	single nucleotide variant	NM_001080503.3(CCDC159):c.350G>A (p.Arg117His)	not specified [RCV004434966]	uncertain significance	19	11350931	11350931	Human		name
405769092	CV3303124	single nucleotide variant	NM_001080503.3(CCDC159):c.416G>A (p.Arg139Gln)	not specified [RCV004434967]	uncertain significance	19	11350997	11350997	Human		name
405769098	CV3303125	single nucleotide variant	NM_001080503.3(CCDC159):c.530T>C (p.Ile177Thr)	not specified [RCV004434968]	uncertain significance	19	11352096	11352096	Human		name
405769107	CV3303126	single nucleotide variant	NM_001080503.3(CCDC159):c.607G>A (p.Ala203Thr)	not specified [RCV004434969]	uncertain significance	19	11353490	11353490	Human		name
405769113	CV3303127	single nucleotide variant	NM_001080503.3(CCDC159):c.614C>T (p.Pro205Leu)	not specified [RCV004434970]	uncertain significance	19	11353497	11353497	Human		name
405769117	CV3303128	single nucleotide variant	NM_001080503.3(CCDC159):c.702C>G (p.His234Gln)	not specified [RCV004434971]	uncertain significance	19	11353804	11353804	Human		name
405769123	CV3303129	single nucleotide variant	NM_001080503.3(CCDC159):c.740C>T (p.Ser247Leu)	not specified [RCV004434972]	likely benign	19	11353842	11353842	Human		name
407484185	CV3418379	single nucleotide variant	NM_001080503.3(CCDC159):c.563G>A (p.Arg188His)	not specified [RCV004602966]	uncertain significance	19	11352129	11352129	Human		name
407454375	CV3418380	single nucleotide variant	NM_001080503.3(CCDC159):c.742G>A (p.Gly248Arg)	not specified [RCV004609836]	uncertain significance	19	11353844	11353844	Human		name
597787241	CV3647843	single nucleotide variant	NM_001080503.3(CCDC159):c.754A>G (p.Lys252Glu)	not specified [RCV004901180]	uncertain significance	19	11353856	11353856	Human		name
597760967	CV3647844	single nucleotide variant	NM_001080503.3(CCDC159):c.719T>C (p.Ile240Thr)	not specified [RCV004894880]	uncertain significance	19	11353821	11353821	Human		name
597787245	CV3647845	single nucleotide variant	NM_001080503.3(CCDC159):c.410A>G (p.Glu137Gly)	not specified [RCV004901181]	uncertain significance	19	11350991	11350991	Human		name
597787249	CV3647846	single nucleotide variant	NM_001080503.3(CCDC159):c.305A>C (p.Tyr102Ser)	not specified [RCV004901182]	uncertain significance	19	11350886	11350886	Human		name
597787253	CV3647847	single nucleotide variant	NM_001080503.3(CCDC159):c.686T>G (p.Ile229Arg)	not specified [RCV004901183]	uncertain significance	19	11353569	11353569	Human		name
597787257	CV3647848	single nucleotide variant	NM_001080503.3(CCDC159):c.715T>C (p.Ser239Pro)	not specified [RCV004901184]	uncertain significance	19	11353817	11353817	Human		name

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