Ppm1h Variant Search Result - Rat Genome Database

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45 records found for search term Ppm1h

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8654127	CV130702	single nucleotide variant	NM_020700.1(PPM1H):c.757-2981T>G	Lung cancer [RCV000111189]	uncertain significance	12	62791319	62791319	Human		name
155963941	CV2194195	single nucleotide variant	NM_020700.2(PPM1H):c.94G>A (p.Gly32Ser)	not specified [RCV004077276]	uncertain significance	12	62934643	62934643	Human		name
401768022	CV2735134	single nucleotide variant	NM_020700.2(PPM1H):c.76G>A (p.Gly26Ser)	not specified [RCV004333831]	uncertain significance	12	62934661	62934661	Human		name
405794884	CV3366490	single nucleotide variant	NM_020700.2(PPM1H):c.52G>C (p.Ala18Pro)	not specified [RCV004507192]	uncertain significance	12	62934685	62934685	Human		name
598168849	CV3897476	single nucleotide variant	NM_020700.2(PPM1H):c.95G>A (p.Gly32Asp)	not specified [RCV005262688]	uncertain significance	12	62934642	62934642	Human		name
156227763	CV2234840	single nucleotide variant	NM_020700.2(PPM1H):c.124G>C (p.Gly42Arg)	not specified [RCV004599469]	uncertain significance	12	62934613	62934613	Human		name
407482974	CV3471506	single nucleotide variant	NM_020700.2(PPM1H):c.118C>G (p.Pro40Ala)	not specified [RCV004664865]	uncertain significance	12	62934619	62934619	Human		name
155918785	CV2254738	single nucleotide variant	NM_020700.2(PPM1H):c.410C>T (p.Ser137Leu)	not specified [RCV004115212]	uncertain significance	12	62832115	62832115	Human		name
156164863	CV2348545	single nucleotide variant	NM_020700.2(PPM1H):c.650G>T (p.Gly217Val)	not specified [RCV004193727]	uncertain significance	12	62801922	62801922	Human		name
156098717	CV2370814	single nucleotide variant	NM_020700.2(PPM1H):c.991A>G (p.Thr331Ala)	not specified [RCV004209207]	uncertain significance	12	62720253	62720253	Human		name
156263900	CV2388907	single nucleotide variant	NM_020700.2(PPM1H):c.611G>A (p.Arg204Gln)	not specified [RCV004241911]	uncertain significance	12	62801961	62801961	Human		name
329386496	CV2428272	single nucleotide variant	NM_020700.2(PPM1H):c.364C>T (p.Arg122Trp)	not specified [RCV004251300]	uncertain significance	12	62832161	62832161	Human		name
329383096	CV2441837	single nucleotide variant	NM_020700.2(PPM1H):c.766A>T (p.Ile256Leu)	not specified [RCV004262036]	uncertain significance	12	62788329	62788329	Human		name
329383208	CV2442018	single nucleotide variant	NM_020700.2(PPM1H):c.935G>A (p.Arg312His)	not specified [RCV004262181]	uncertain significance	12	62737521	62737521	Human		name
329373899	CV2447474	single nucleotide variant	NM_020700.2(PPM1H):c.437A>G (p.Tyr146Cys)	not specified [RCV004255838]	uncertain significance	12	62802135	62802135	Human		name
401736871	CV2699617	single nucleotide variant	NM_020700.2(PPM1H):c.887A>G (p.Asn296Ser)	not specified [RCV004299804]	uncertain significance	12	62737569	62737569	Human		name
405794881	CV3366489	single nucleotide variant	NM_020700.2(PPM1H):c.316A>G (p.Lys106Glu)	not specified [RCV004507191]	uncertain significance	12	62832209	62832209	Human		name
405794887	CV3366491	single nucleotide variant	NM_020700.2(PPM1H):c.695A>T (p.Glu232Val)	not specified [RCV004507193]	uncertain significance	12	62801877	62801877	Human		name
405794890	CV3366492	single nucleotide variant	NM_020700.2(PPM1H):c.821T>C (p.Val274Ala)	not specified [RCV004507194]	uncertain significance	12	62788274	62788274	Human		name
407529700	CV3471505	single nucleotide variant	NM_020700.2(PPM1H):c.685T>G (p.Phe229Val)	not specified [RCV004656172]	uncertain significance	12	62801887	62801887	Human		name
407529702	CV3471507	single nucleotide variant	NM_020700.2(PPM1H):c.742G>A (p.Ala248Thr)	not specified [RCV004656173]	uncertain significance	12	62801830	62801830	Human		name
597758293	CV3591357	single nucleotide variant	NM_020700.2(PPM1H):c.773G>A (p.Arg258Gln)	not specified [RCV004848503]	uncertain significance	12	62788322	62788322	Human		name
597758298	CV3591358	single nucleotide variant	NM_020700.2(PPM1H):c.938A>G (p.Gln313Arg)	not specified [RCV004848504]	uncertain significance	12	62737518	62737518	Human		name
597758303	CV3591359	single nucleotide variant	NM_020700.2(PPM1H):c.356C>G (p.Ser119Cys)	not specified [RCV004848505]	uncertain significance	12	62832169	62832169	Human		name
597758312	CV3591361	single nucleotide variant	NM_020700.2(PPM1H):c.562C>T (p.Pro188Ser)	not specified [RCV004848507]	uncertain significance	12	62802010	62802010	Human		name
597758322	CV3591363	single nucleotide variant	NM_020700.2(PPM1H):c.365G>T (p.Arg122Leu)	not specified [RCV004848509]	uncertain significance	12	62832160	62832160	Human		name
15165063	CV713690	single nucleotide variant	NM_020700.2(PPM1H):c.613A>C (p.Thr205Pro)	not provided [RCV000970870]	benign	12	62801959	62801959	Human		name
156164993	CV2270307	single nucleotide variant	NM_020700.2(PPM1H):c.1430G>A (p.Arg477His)	not specified [RCV004135519]	uncertain significance	12	62648604	62648604	Human		name
155925666	CV2277341	single nucleotide variant	NM_020700.2(PPM1H):c.1141C>T (p.Arg381Trp)	not specified [RCV004144766]	uncertain significance	12	62689803	62689803	Human		name
156202845	CV2300675	single nucleotide variant	NM_020700.2(PPM1H):c.1408G>T (p.Ala470Ser)	not specified [RCV004155619]	uncertain significance	12	62648626	62648626	Human		name
156202855	CV2300676	single nucleotide variant	NM_020700.2(PPM1H):c.1409C>T (p.Ala470Val)	not specified [RCV004155620]	uncertain significance	12	62648625	62648625	Human		name
156255413	CV2311603	single nucleotide variant	NM_020700.2(PPM1H):c.1462C>T (p.Arg488Trp)	not specified [RCV004168413]	uncertain significance	12	62648572	62648572	Human		name
156307308	CV2312256	single nucleotide variant	NM_020700.2(PPM1H):c.1088T>C (p.Ile363Thr)	not specified [RCV004166970]	uncertain significance	12	62693985	62693985	Human		name
329360363	CV2442743	single nucleotide variant	NM_020700.2(PPM1H):c.1402A>G (p.Thr468Ala)	not specified [RCV004251579]	uncertain significance	12	62648632	62648632	Human		name
401897811	CV2772942	single nucleotide variant	NM_020700.2(PPM1H):c.1271A>G (p.Tyr424Cys)	not specified [RCV004357710]	uncertain significance	12	62667304	62667304	Human		name
405794875	CV3366487	single nucleotide variant	NM_020700.2(PPM1H):c.1066A>G (p.Thr356Ala)	not specified [RCV004507189]	uncertain significance	12	62720178	62720178	Human		name
405794878	CV3366488	single nucleotide variant	NM_020700.2(PPM1H):c.1207A>G (p.Asn403Asp)	not specified [RCV004507190]	uncertain significance	12	62689737	62689737	Human		name
407529704	CV3471509	single nucleotide variant	NM_020700.2(PPM1H):c.1471A>G (p.Asn491Asp)	not specified [RCV004656174]	uncertain significance	12	62648563	62648563	Human		name
597758308	CV3591360	single nucleotide variant	NM_020700.2(PPM1H):c.1494C>A (p.Asp498Glu)	not specified [RCV004848506]	uncertain significance	12	62648540	62648540	Human		name
597758316	CV3591362	single nucleotide variant	NM_020700.2(PPM1H):c.1133A>G (p.Lys378Arg)	not specified [RCV004848508]	uncertain significance	12	62693940	62693940	Human		name
598168837	CV3897474	single nucleotide variant	NM_020700.2(PPM1H):c.1463G>A (p.Arg488Gln)	not specified [RCV005262686]	uncertain significance	12	62648571	62648571	Human		name
598168844	CV3897475	single nucleotide variant	NM_020700.2(PPM1H):c.1535A>C (p.Lys512Thr)	not specified [RCV005262687]	uncertain significance	12	62648499	62648499	Human		name
598168856	CV3897477	single nucleotide variant	NM_020700.2(PPM1H):c.1142G>A (p.Arg381Gln)	not specified [RCV005262689]	uncertain significance	12	62689802	62689802	Human		name
598168861	CV3897478	single nucleotide variant	NM_020700.2(PPM1H):c.1157T>C (p.Ile386Thr)	not specified [RCV005262690]	uncertain significance	12	62689787	62689787	Human		name
598168866	CV3897479	single nucleotide variant	NM_020700.2(PPM1H):c.1417G>A (p.Asp473Asn)	not specified [RCV005262691]	uncertain significance	12	62648617	62648617	Human		name

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