Ppp1r9a Variant Search Result - Rat Genome Database

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147 records found for search term Ppp1r9a

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8649634	CV126208	single nucleotide variant	NM_001166160.1(PPP1R9A):c.*4194G>T	Lung cancer [RCV000106695]	uncertain significance	7	95294497	95294497	Human		name
405275766	CV3199415	single nucleotide variant	NM_001166160.2(PPP1R9A):c.2493+4A>C	PPP1R9A-related disorder [RCV003916824]	benign	7	95251862	95251863	Human	1	name , trait , alternate_id
405275766	CV3199415	single nucleotide variant	NM_001166160.2(PPP1R9A):c.2493+4A>C	PPP1R9A-related disorder [RCV003916824]	benign	7	95251862	95251862	Human	1	name , trait , alternate_id
405276423	CV3206730	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3124+9A>C	PPP1R9A-related disorder [RCV003917165]	benign	7	95269516	95269516	Human		name , trait , alternate_id
8649633	CV126207	single nucleotide variant	NM_001166160.1(PPP1R9A):c.3297-263A>G	Lung cancer [RCV000106694]	uncertain significance	7	95283755	95283755	Human		name
8649629	CV126203	single nucleotide variant	NM_001166160.1(PPP1R9A):c.1528+1320C>A	Lung cancer [RCV000106690]	uncertain significance	7	95112711	95112711	Human		name
8649632	CV126206	single nucleotide variant	NM_001166160.1(PPP1R9A):c.2666-6630C>A	Lung cancer [RCV000106693]	uncertain significance	7	95261920	95261920	Human		name
8649625	CV126199	single nucleotide variant	NM_001166160.1(PPP1R9A):c.1396-91947G>T	Lung cancer [RCV000106686]	uncertain significance	7	95019312	95019312	Human		name
8649627	CV126201	single nucleotide variant	NM_001166160.1(PPP1R9A):c.1396-60807G>T	Lung cancer [RCV000106688]	uncertain significance	7	95050452	95050452	Human		name
8649628	CV126202	single nucleotide variant	NM_001166160.1(PPP1R9A):c.1396-13059C>G	Lung cancer [RCV000106689]	uncertain significance	7	95098200	95098200	Human		name
8649630	CV126204	single nucleotide variant	NM_001166160.1(PPP1R9A):c.1649+15081C>A	Lung cancer [RCV000106691]	uncertain significance	7	95135913	95135913	Human		name
8649631	CV126205	single nucleotide variant	NM_001166160.1(PPP1R9A):c.1650-18214G>T	Lung cancer [RCV000106692]	uncertain significance	7	95143653	95143653	Human		name
405287978	CV3218023	single nucleotide variant	NM_001166160.2(PPP1R9A):c.111C>T (p.Pro37=)	PPP1R9A-related disorder [RCV003982147]	benign	7	94910224	94910224	Human		name , trait , alternate_id
329393300	CV2449639	single nucleotide variant	NM_001166160.2(PPP1R9A):c.34A>G (p.Thr12Ala)	not specified [RCV004268554]	uncertain significance	7	94910147	94910147	Human		name
405275643	CV3216028	single nucleotide variant	NM_001166160.2(PPP1R9A):c.393C>T (p.Tyr131=)	PPP1R9A-related disorder [RCV003952292]	likely benign	7	94910506	94910506	Human		name , trait , alternate_id
598169952	CV3907681	single nucleotide variant	NM_001166160.2(PPP1R9A):c.76G>C (p.Glu26Gln)	not specified [RCV005262949]	uncertain significance	7	94910189	94910189	Human		name
156361455	CV2269248	single nucleotide variant	NM_001166160.2(PPP1R9A):c.125A>T (p.Glu42Val)	not specified [RCV004130396]	uncertain significance	7	94910238	94910238	Human		name
156061793	CV2392041	single nucleotide variant	NM_001166160.2(PPP1R9A):c.233A>G (p.Asn78Ser)	not specified [RCV004235892]	likely benign	7	94910346	94910346	Human		name
405287167	CV3193115	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1362T>C (p.Asn454=)	PPP1R9A-related disorder [RCV003981767]	likely benign	7	94911475	94911475	Human		name , trait , alternate_id
405272318	CV3199323	single nucleotide variant	NM_001166160.2(PPP1R9A):c.2889G>A (p.Thr963=)	PPP1R9A-related disorder [RCV003914273]	likely benign	7	95269272	95269272	Human		name , trait , alternate_id
597769254	CV3587889	single nucleotide variant	NM_001166160.2(PPP1R9A):c.265G>A (p.Gly89Arg)	not specified [RCV004850882]	uncertain significance	7	94910378	94910378	Human		name
15197580	CV700302	single nucleotide variant	NM_001166160.2(PPP1R9A):c.115T>A (p.Ser39Thr)	not provided [RCV000956505]	benign	7	94910228	94910228	Human		name
15102967	CV722749	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1512A>G (p.Pro504=)	PPP1R9A-related disorder [RCV003968147]\|not provided [RCV000892582]	benign\|likely benign	7	95111375	95111375	Human		name , trait , alternate_id
150464380	CV1273299	single nucleotide variant	NM_001166160.2(PPP1R9A):c.991A>G (p.Met331Val)	PPP1R9A-related disorder [RCV003956325]\|not provided [RCV001694056]	benign	7	94911104	94911104	Human		name , trait , alternate_id
156075438	CV2248247	single nucleotide variant	NM_001166160.2(PPP1R9A):c.300G>A (p.Met100Ile)	not specified [RCV004119418]	uncertain significance	7	94910413	94910413	Human		name
155952804	CV2306207	single nucleotide variant	NM_001166160.2(PPP1R9A):c.847G>C (p.Ala283Pro)	not specified [RCV004162949]	uncertain significance	7	94910960	94910960	Human		name
156195322	CV2306631	single nucleotide variant	NM_001166160.2(PPP1R9A):c.812C>T (p.Ala271Val)	not specified [RCV004157229]	uncertain significance	7	94910925	94910925	Human		name
156293256	CV2321292	single nucleotide variant	NM_001166160.2(PPP1R9A):c.731C>A (p.Thr244Lys)	not specified [RCV004177306]	uncertain significance	7	94910844	94910844	Human		name
156198592	CV2362803	single nucleotide variant	NM_001166160.2(PPP1R9A):c.350A>G (p.Glu117Gly)	not specified [RCV004208920]	uncertain significance	7	94910463	94910463	Human		name
156305255	CV2369408	single nucleotide variant	NM_001166160.2(PPP1R9A):c.460G>A (p.Gly154Arg)	not specified [RCV004210354]	uncertain significance	7	94910573	94910573	Human		name
401735982	CV2689227	single nucleotide variant	NM_001166160.2(PPP1R9A):c.581G>C (p.Arg194Pro)	not specified [RCV004306072]	uncertain significance	7	94910694	94910694	Human		name
401862395	CV2775282	single nucleotide variant	NM_001166160.2(PPP1R9A):c.931C>G (p.Gln311Glu)	not specified [RCV004348402]	likely benign	7	94911044	94911044	Human		name
401895132	CV2792801	single nucleotide variant	NM_001166160.2(PPP1R9A):c.935C>G (p.Thr312Ser)	not specified [RCV004365555]	uncertain significance	7	94911048	94911048	Human		name
401922573	CV2825877	single nucleotide variant	NM_001166160.2(PPP1R9A):c.802A>T (p.Thr268Ser)	not provided [RCV003433940]	likely benign	7	94910915	94910915	Human		name
405293799	CV3214570	single nucleotide variant	NM_001166160.2(PPP1R9A):c.4104C>T (p.Ala1368=)	PPP1R9A-related disorder [RCV003932239]	likely benign	7	95290282	95290282	Human		name , trait , alternate_id
405287892	CV3217976	single nucleotide variant	NM_001166160.2(PPP1R9A):c.4035A>G (p.Leu1345=)	PPP1R9A-related disorder [RCV003982100]	benign	7	95290213	95290213	Human		name , trait , alternate_id
405267060	CV3218716	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3216G>A (p.Ala1072=)	PPP1R9A-related disorder [RCV003947309]	likely benign	7	95274088	95274088	Human		name , trait , alternate_id
405652983	CV3377014	single nucleotide variant	NM_001166160.2(PPP1R9A):c.431A>C (p.Lys144Thr)	not specified [RCV004510049]	uncertain significance	7	94910544	94910544	Human		name
405652984	CV3377015	single nucleotide variant	NM_001166160.2(PPP1R9A):c.609T>A (p.Ser203Arg)	not specified [RCV004510050]	uncertain significance	7	94910722	94910722	Human		name
407529888	CV3467790	single nucleotide variant	NM_001166160.2(PPP1R9A):c.900C>A (p.Ser300Arg)	not specified [RCV004656291]	uncertain significance	7	94911013	94911013	Human		name
407464563	CV3467792	single nucleotide variant	NM_001166160.2(PPP1R9A):c.581G>A (p.Arg194Gln)	not specified [RCV004659983]	uncertain significance	7	94910694	94910694	Human		name
597769207	CV3587879	single nucleotide variant	NM_001166160.2(PPP1R9A):c.892C>G (p.Gln298Glu)	not specified [RCV004850872]	uncertain significance	7	94911005	94911005	Human		name
597769215	CV3587881	single nucleotide variant	NM_001166160.2(PPP1R9A):c.898A>C (p.Ser300Arg)	not specified [RCV004850874]	uncertain significance	7	94911011	94911011	Human		name
597769231	CV3587884	single nucleotide variant	NM_001166160.2(PPP1R9A):c.984T>G (p.Ser328Arg)	not specified [RCV004850877]	uncertain significance	7	94911097	94911097	Human		name
597769239	CV3587886	single nucleotide variant	NM_001166160.2(PPP1R9A):c.556G>C (p.Asp186His)	not specified [RCV004850879]	uncertain significance	7	94910669	94910669	Human		name
598169931	CV3897735	single nucleotide variant	NM_001166160.2(PPP1R9A):c.470A>G (p.Asn157Ser)	not specified [RCV005262942]	uncertain significance	7	94910583	94910583	Human		name
598169934	CV3897736	single nucleotide variant	NM_001166160.2(PPP1R9A):c.380T>C (p.Phe127Ser)	not specified [RCV005262943]	uncertain significance	7	94910493	94910493	Human		name
15133959	CV711199	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3012C>G (p.Leu1004=)	PPP1R9A-related disorder [RCV003916171]\|not provided [RCV000965043]	benign	7	95269395	95269395	Human		name , trait , alternate_id
156316095	CV2193007	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1316A>G (p.Tyr439Cys)	not specified [RCV004069558]	uncertain significance	7	94911429	94911429	Human		name
156236206	CV2224105	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1793A>T (p.Glu598Val)	not specified [RCV004095969]	uncertain significance	7	95198387	95198387	Human		name
156071496	CV2254900	single nucleotide variant	NM_001166160.2(PPP1R9A):c.2743A>G (p.Asn915Asp)	not specified [RCV004117143]	uncertain significance	7	95268627	95268627	Human		name
156149822	CV2265375	single nucleotide variant	NM_001166160.2(PPP1R9A):c.2817G>C (p.Glu939Asp)	not specified [RCV004128258]	uncertain significance	7	95268701	95268701	Human		name
156153712	CV2266017	single nucleotide variant	NM_001166160.2(PPP1R9A):c.2063T>A (p.Phe688Tyr)	not specified [RCV004126840]	uncertain significance	7	95226067	95226067	Human		name
156018811	CV2272388	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1298A>G (p.Tyr433Cys)	not specified [RCV004133312]	uncertain significance	7	94911411	94911411	Human		name
156161319	CV2272579	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1422C>G (p.Asp474Glu)	not specified [RCV004133466]	uncertain significance	7	95111285	95111285	Human		name
155955028	CV2274406	single nucleotide variant	NM_001166160.2(PPP1R9A):c.2939G>A (p.Ser980Asn)	not specified [RCV004136778]	uncertain significance	7	95269322	95269322	Human		name
156169280	CV2276720	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1908G>T (p.Leu636Phe)	not specified [RCV004146509]	uncertain significance	7	95203682	95203682	Human		name
156006757	CV2288908	single nucleotide variant	NM_001166160.2(PPP1R9A):c.2720C>G (p.Thr907Ser)	not specified [RCV004149878]	uncertain significance	7	95268604	95268604	Human		name
156086514	CV2289964	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1126G>T (p.Ala376Ser)	not specified [RCV004150613]	uncertain significance	7	94911239	94911239	Human		name
156272133	CV2308752	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1993G>A (p.Val665Ile)	not specified [RCV004169074]	uncertain significance	7	95225997	95225997	Human		name
156265017	CV2312168	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1211A>G (p.Tyr404Cys)	not specified [RCV004165071]	uncertain significance	7	94911324	94911324	Human		name
156071959	CV2325265	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1055T>C (p.Val352Ala)	not specified [RCV004177663]	uncertain significance	7	94911168	94911168	Human		name
156121265	CV2354241	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1048A>G (p.Asn350Asp)	not specified [RCV004206665]	uncertain significance	7	94911161	94911161	Human		name
156013004	CV2359003	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1289A>G (p.Asn430Ser)	not specified [RCV004212330]	uncertain significance	7	94911402	94911402	Human		name
329375147	CV2431392	single nucleotide variant	NM_001166160.2(PPP1R9A):c.2548G>A (p.Val850Ile)	not specified [RCV004254558]	uncertain significance	7	95252013	95252013	Human		name
329391978	CV2445234	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1900G>A (p.Ala634Thr)	not specified [RCV004263867]	uncertain significance	7	95203674	95203674	Human		name
329400847	CV2449760	single nucleotide variant	NM_001166160.2(PPP1R9A):c.2069C>T (p.Pro690Leu)	not specified [RCV004270437]	uncertain significance	7	95226073	95226073	Human		name
401749731	CV2710939	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1907T>G (p.Leu636Trp)	not specified [RCV004310656]	uncertain significance	7	95203681	95203681	Human		name
401765273	CV2712590	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1886A>G (p.Asp629Gly)	not specified [RCV004307919]	uncertain significance	7	95198480	95198480	Human		name
401764042	CV2717206	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1522G>C (p.Glu508Gln)	not specified [RCV004324060]	uncertain significance	7	95111385	95111385	Human		name
401887778	CV2772191	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1093G>A (p.Ala365Thr)	not specified [RCV004346838]	uncertain significance	7	94911206	94911206	Human		name
401858131	CV2774206	single nucleotide variant	NM_001166160.2(PPP1R9A):c.2696G>C (p.Arg899Pro)	not specified [RCV004347582]	uncertain significance	7	95268580	95268580	Human		name
401908857	CV2825878	single nucleotide variant	NM_001166160.2(PPP1R9A):c.2750G>A (p.Arg917His)	not provided [RCV003423649]	uncertain significance	7	95268634	95268634	Human		name
405264998	CV3201447	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1162A>C (p.Asn388His)	PPP1R9A-related disorder [RCV003897205]	likely benign	7	94911275	94911275	Human		name , trait , alternate_id
405256085	CV3208645	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1198G>A (p.Asp400Asn)	PPP1R9A-related disorder [RCV003939711]	likely benign	7	94911311	94911311	Human		name , trait , alternate_id
405287519	CV3217823	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1102G>A (p.Asp368Asn)	PPP1R9A-related disorder [RCV003981946]	benign	7	94911215	94911215	Human	4	name , trait , alternate_id
405285838	CV3221637	single nucleotide variant	NM_001166160.2(PPP1R9A):c.2480G>C (p.Gly827Ala)	PPP1R9A-related disorder [RCV003981344]	benign	7	95251845	95251845	Human		name , trait , alternate_id
405652940	CV3376991	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1009C>T (p.Pro337Ser)	not specified [RCV004510026]	uncertain significance	7	94911122	94911122	Human		name
405652944	CV3376993	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1190T>C (p.Met397Thr)	not specified [RCV004510028]	uncertain significance	7	94911303	94911303	Human		name
405652946	CV3376994	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1264G>A (p.Asp422Asn)	not specified [RCV004510029]	uncertain significance	7	94911377	94911377	Human		name
405652948	CV3376995	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1310T>C (p.Met437Thr)	not specified [RCV004510030]	uncertain significance	7	94911423	94911423	Human		name
405652950	CV3376996	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1325T>C (p.Ile442Thr)	not specified [RCV004510031]	uncertain significance	7	94911438	94911438	Human		name
405652952	CV3376997	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1340A>C (p.Glu447Ala)	not specified [RCV004510032]	uncertain significance	7	94911453	94911453	Human		name
405652953	CV3376998	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1345G>A (p.Glu449Lys)	not specified [RCV004510033]	uncertain significance	7	94911458	94911458	Human		name
405653056	CV3376999	single nucleotide variant	NM_001166160.2(PPP1R9A):c.2566A>G (p.Ile856Val)	not specified [RCV004510034]	uncertain significance	7	95252031	95252031	Human		name
405652957	CV3377000	single nucleotide variant	NM_001166160.2(PPP1R9A):c.2867T>G (p.Leu956Arg)	not specified [RCV004510035]	uncertain significance	7	95269250	95269250	Human		name
405652959	CV3377001	single nucleotide variant	NM_001166160.2(PPP1R9A):c.2899G>A (p.Glu967Lys)	not specified [RCV004510036]	uncertain significance	7	95269282	95269282	Human		name
405652961	CV3377002	single nucleotide variant	NM_001166160.2(PPP1R9A):c.2930C>T (p.Pro977Leu)	not specified [RCV004510037]	uncertain significance	7	95269313	95269313	Human		name
405652963	CV3377003	single nucleotide variant	NM_001166160.2(PPP1R9A):c.2935G>A (p.Asp979Asn)	not specified [RCV004510038]	uncertain significance	7	95269318	95269318	Human		name
407529886	CV3467787	single nucleotide variant	NM_001166160.2(PPP1R9A):c.2947C>A (p.Pro983Thr)	not specified [RCV004656289]	uncertain significance	7	95269330	95269330	Human		name
407464559	CV3467791	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1304C>T (p.Pro435Leu)	not specified [RCV004659982]	uncertain significance	7	94911417	94911417	Human		name
407464571	CV3467794	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1015C>A (p.Pro339Thr)	not specified [RCV004659985]	uncertain significance	7	94911128	94911128	Human		name
407529889	CV3467795	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1080G>C (p.Gln360His)	not specified [RCV004656292]	uncertain significance	7	94911193	94911193	Human		name
407464576	CV3467796	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1134T>G (p.Ser378Arg)	not specified [RCV004659986]	uncertain significance	7	94911247	94911247	Human		name
407529890	CV3467797	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1651A>G (p.Ile551Val)	not specified [RCV004656293]	uncertain significance	7	95161868	95161868	Human		name
597769191	CV3587876	single nucleotide variant	NM_001166160.2(PPP1R9A):c.2101A>G (p.Lys701Glu)	not specified [RCV004850869]	uncertain significance	7	95226105	95226105	Human		name
597769197	CV3587877	single nucleotide variant	NM_001166160.2(PPP1R9A):c.2322G>C (p.Glu774Asp)	not specified [RCV004850870]	uncertain significance	7	95250181	95250181	Human		name
597769202	CV3587878	single nucleotide variant	NM_001166160.2(PPP1R9A):c.2950T>C (p.Phe984Leu)	not specified [RCV004850871]	uncertain significance	7	95269333	95269333	Human		name
597769211	CV3587880	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1076A>C (p.Gln359Pro)	not specified [RCV004850873]	uncertain significance	7	94911189	94911189	Human		name
597769234	CV3587885	single nucleotide variant	NM_001166160.2(PPP1R9A):c.2224C>A (p.Gln742Lys)	not specified [RCV004850878]	uncertain significance	7	95250083	95250083	Human		name
597769258	CV3587890	single nucleotide variant	NM_001166160.2(PPP1R9A):c.2165A>T (p.Lys722Met)	not specified [RCV004850883]	uncertain significance	7	95247525	95247525	Human		name
598169929	CV3897734	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1211A>T (p.Tyr404Phe)	not specified [RCV005262941]	uncertain significance	7	94911324	94911324	Human		name
598169939	CV3907677	single nucleotide variant	NM_001166160.2(PPP1R9A):c.2458G>A (p.Ala820Thr)	not specified [RCV005262945]	uncertain significance	7	95251823	95251823	Human		name
598169945	CV3907679	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1133G>T (p.Ser378Ile)	not specified [RCV005262947]	uncertain significance	7	94911246	94911246	Human		name
598169958	CV3907683	single nucleotide variant	NM_001166160.2(PPP1R9A):c.1987G>C (p.Asp663His)	not specified [RCV005262951]	uncertain significance	7	95225991	95225991	Human		name
598169961	CV3907684	single nucleotide variant	NM_001166160.2(PPP1R9A):c.2966T>C (p.Ile989Thr)	not specified [RCV005262952]	uncertain significance	7	95269349	95269349	Human		name
15168710	CV700303	single nucleotide variant	NM_001166160.2(PPP1R9A):c.2749C>T (p.Arg917Cys)	PPP1R9A-related disorder [RCV003903190]\|not provided [RCV000949314]	benign	7	95268633	95268633	Human		name , trait , alternate_id
156027059	CV2199263	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3565A>G (p.Arg1189Gly)	not specified [RCV004082618]	uncertain significance	7	95284286	95284286	Human		name
156144489	CV2208754	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3224G>A (p.Arg1075Gln)	not specified [RCV004084940]	uncertain significance	7	95274096	95274096	Human		name
156379818	CV2211594	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3206A>G (p.Asp1069Gly)	not specified [RCV004084492]	uncertain significance	7	95273980	95273980	Human		name
156252955	CV2212495	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3194G>A (p.Arg1065Gln)	not specified [RCV004091381]	likely benign	7	95273968	95273968	Human		name
156133717	CV2235443	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3230A>C (p.Asn1077Thr)	not specified [RCV004109491]	uncertain significance	7	95274102	95274102	Human		name
156347071	CV2297813	single nucleotide variant	NM_001166160.2(PPP1R9A):c.4121A>G (p.Gln1374Arg)	not specified [RCV004157762]	uncertain significance	7	95290299	95290299	Human		name
156336710	CV2342941	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3090C>A (p.His1030Gln)	not specified [RCV004192549]	uncertain significance	7	95269473	95269473	Human		name
156086001	CV2390763	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3941G>A (p.Arg1314Gln)	not specified [RCV004241052]	uncertain significance	7	95290119	95290119	Human		name
329372593	CV2451559	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3193C>T (p.Arg1065Trp)	not specified [RCV004274496]	uncertain significance	7	95273967	95273967	Human		name
401772614	CV2719696	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3014C>T (p.Ser1005Phe)	not specified [RCV004329137]	uncertain significance	7	95269397	95269397	Human		name
401780944	CV2734035	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3560T>G (p.Phe1187Cys)	not specified [RCV004330596]	uncertain significance	7	95284281	95284281	Human		name
401882847	CV2775126	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3275G>A (p.Ser1092Asn)	not specified [RCV004346485]	likely benign	7	95274147	95274147	Human		name
405292366	CV3192340	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3293G>A (p.Ser1098Asn)	PPP1R9A-related disorder [RCV003929618]	benign	7	95274165	95274165	Human	1	name , trait , alternate_id
405288410	CV3197421	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3236G>A (p.Ser1079Asn)	PPP1R9A-related disorder [RCV003982517]	benign	7	95274108	95274108	Human		name , trait , alternate_id
405284040	CV3200499	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3116G>A (p.Arg1039Gln)	PPP1R9A-related disorder [RCV003979518]	benign	7	95269499	95269499	Human		name , trait , alternate_id
405287123	CV3205621	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3860C>A (p.Ala1287Asp)	PPP1R9A-related disorder [RCV003959758]	likely benign	7	95288666	95288666	Human		name , trait , alternate_id
405652965	CV3377004	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3004G>T (p.Gly1002Trp)	not specified [RCV004510039]	uncertain significance	7	95269387	95269387	Human		name
405652967	CV3377005	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3019A>G (p.Met1007Val)	not specified [RCV004510040]	likely benign	7	95269402	95269402	Human		name
405652969	CV3377006	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3020T>C (p.Met1007Thr)	not specified [RCV004510041]	uncertain significance	7	95269403	95269403	Human		name
405652973	CV3377008	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3211G>A (p.Gly1071Arg)	not specified [RCV004510043]	uncertain significance	7	95273985	95273985	Human		name
405652975	CV3377009	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3394G>A (p.Asp1132Asn)	not specified [RCV004510044]	uncertain significance	7	95284115	95284115	Human		name
405652977	CV3377010	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3401G>A (p.Arg1134Gln)	not specified [RCV004510045]	uncertain significance	7	95284122	95284122	Human		name
405652978	CV3377011	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3478G>A (p.Asp1160Asn)	not specified [RCV004510046]	uncertain significance	7	95284199	95284199	Human		name
405652980	CV3377012	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3506C>T (p.Thr1169Ile)	not specified [RCV004510047]	uncertain significance	7	95284227	95284227	Human		name
405652982	CV3377013	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3995G>A (p.Arg1332Gln)	not specified [RCV004510048]	uncertain significance	7	95290173	95290173	Human		name
407464551	CV3467786	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3697C>T (p.Leu1233Phe)	not specified [RCV004659980]	uncertain significance	7	95286293	95286293	Human		name
407529887	CV3467789	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3101A>G (p.Asn1034Ser)	not specified [RCV004656290]	uncertain significance	7	95269484	95269484	Human		name
407464567	CV3467793	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3253A>G (p.Lys1085Glu)	not specified [RCV004659984]	uncertain significance	7	95274125	95274125	Human		name
407529891	CV3467798	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3242G>A (p.Gly1081Glu)	not specified [RCV004656294]	uncertain significance	7	95274114	95274114	Human		name
597769221	CV3587882	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3373A>G (p.Met1125Val)	not specified [RCV004850875]	uncertain significance	7	95284094	95284094	Human		name
597769226	CV3587883	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3143A>G (p.Lys1048Arg)	not specified [RCV004850876]	uncertain significance	7	95273917	95273917	Human		name
597769244	CV3587887	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3859G>A (p.Ala1287Thr)	not specified [RCV004850880]	uncertain significance	7	95288665	95288665	Human		name
597769248	CV3587888	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3248A>G (p.Lys1083Arg)	not specified [RCV004850881]	uncertain significance	7	95274120	95274120	Human		name
597769263	CV3587891	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3239A>G (p.Lys1080Arg)	not specified [RCV004850884]	uncertain significance	7	95274111	95274111	Human		name
598169942	CV3907678	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3976A>C (p.Met1326Leu)	not specified [RCV005262946]	uncertain significance	7	95290154	95290154	Human		name
598169949	CV3907680	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3935A>G (p.Gln1312Arg)	not specified [RCV005262948]	uncertain significance	7	95290113	95290113	Human		name
598169955	CV3907682	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3209T>C (p.Leu1070Pro)	not specified [RCV005262950]	uncertain significance	7	95273983	95273983	Human		name
598169964	CV3907685	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3214G>A (p.Ala1072Thr)	not specified [RCV005262953]	uncertain significance	7	95274086	95274086	Human		name
15121530	CV711200	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3374T>C (p.Met1125Thr)	PPP1R9A-related disorder [RCV003926190]\|not provided [RCV000962910]	benign\|likely benign	7	95284095	95284095	Human		name , trait , alternate_id
15198616	CV722750	single nucleotide variant	NM_001166160.2(PPP1R9A):c.3776G>A (p.Arg1259Gln)	PPP1R9A-related disorder [RCV003930774]\|not provided [RCV000890410]	benign	7	95288582	95288582	Human		name , trait , alternate_id

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