Ptrh1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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38 records found for search term Ptrh1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
598250570	CV3901834	single nucleotide variant	NM_001002913.3(PTRH1):c.8C>T (p.Pro3Leu)	not specified [RCV005259077]	uncertain significance	9	127715632	127715632	Human		name
401759052	CV2705355	single nucleotide variant	NM_001002913.3(PTRH1):c.23G>A (p.Gly8Asp)	not specified [RCV004312030]	uncertain significance	9	127715617	127715617	Human		name
405658081	CV3315069	single nucleotide variant	NM_001002913.3(PTRH1):c.11G>A (p.Gly4Asp)	not specified [RCV004438070]	uncertain significance	9	127715629	127715629	Human		name
407486640	CV3464738	single nucleotide variant	NM_001002913.3(PTRH1):c.13G>T (p.Gly5Cys)	not specified [RCV004669279]	uncertain significance	9	127715627	127715627	Human		name
13820737	CV576129	single nucleotide variant	NM_001002913.3(PTRH1):c.20T>C (p.Leu7Ser)	not provided [RCV000709791]	not provided	9	127715620	127715620	Human		name
329363555	CV2442301	single nucleotide variant	NM_001002913.3(PTRH1):c.73C>T (p.Arg25Cys)	not specified [RCV004264779]	uncertain significance	9	127715567	127715567	Human		name
405658089	CV3315072	single nucleotide variant	NM_001002913.3(PTRH1):c.49A>G (p.Met17Val)	not specified [RCV004438073]	uncertain significance	9	127715591	127715591	Human		name
405658092	CV3315073	single nucleotide variant	NM_001002913.3(PTRH1):c.50T>A (p.Met17Lys)	not specified [RCV004438074]	uncertain significance	9	127715590	127715590	Human		name
407486652	CV3464741	single nucleotide variant	NM_001002913.3(PTRH1):c.79C>T (p.Pro27Ser)	not specified [RCV004669281]	uncertain significance	9	127715561	127715561	Human		name
156281654	CV2348795	single nucleotide variant	NM_001002913.3(PTRH1):c.208C>T (p.Arg70Trp)	not specified [RCV004203241]	uncertain significance	9	127715083	127715083	Human		name
156144944	CV2393731	single nucleotide variant	NM_001002913.3(PTRH1):c.192G>C (p.Glu64Asp)	not specified [RCV004231530]	uncertain significance	9	127715099	127715099	Human		name
401750520	CV2715669	single nucleotide variant	NM_001002913.3(PTRH1):c.224A>T (p.Asp75Val)	not specified [RCV004327042]	uncertain significance	9	127715067	127715067	Human		name
401893606	CV2759844	single nucleotide variant	NM_001002913.3(PTRH1):c.203G>T (p.Arg68Leu)	not specified [RCV004343275]	uncertain significance	9	127715088	127715088	Human		name
405658078	CV3315068	single nucleotide variant	NM_001002913.3(PTRH1):c.118G>A (p.Gly40Arg)	not specified [RCV004438069]	uncertain significance	9	127715173	127715173	Human		name
405658082	CV3315070	single nucleotide variant	NM_001002913.3(PTRH1):c.220G>C (p.Ala74Pro)	not specified [RCV004438071]	uncertain significance	9	127715071	127715071	Human		name
597762960	CV3582188	single nucleotide variant	NM_001002913.3(PTRH1):c.173G>A (p.Arg58Gln)	not specified [RCV004849440]	uncertain significance	9	127715118	127715118	Human		name
597762975	CV3582191	single nucleotide variant	NM_001002913.3(PTRH1):c.275G>A (p.Arg92Gln)	not specified [RCV004849443]	uncertain significance	9	127715016	127715016	Human		name
156076066	CV2230187	single nucleotide variant	NM_001002913.3(PTRH1):c.517C>G (p.Gln173Glu)	not specified [RCV004099820]	uncertain significance	9	127714228	127714228	Human		name
156332191	CV2339747	single nucleotide variant	NM_001002913.3(PTRH1):c.433C>T (p.Arg145Cys)	not specified [RCV004196446]	uncertain significance	9	127714408	127714408	Human		name
156279211	CV2348312	single nucleotide variant	NM_001002913.3(PTRH1):c.581G>A (p.Arg194Gln)	not specified [RCV004193512]	uncertain significance	9	127714164	127714164	Human		name
155917841	CV2362425	single nucleotide variant	NM_001002913.3(PTRH1):c.425A>G (p.Asn142Ser)	not specified [RCV004213047]	uncertain significance	9	127714416	127714416	Human		name
329388497	CV2437466	single nucleotide variant	NM_001002913.3(PTRH1):c.497C>T (p.Pro166Leu)	not specified [RCV004256330]	uncertain significance	9	127714248	127714248	Human		name
329372912	CV2451724	single nucleotide variant	NM_001002913.3(PTRH1):c.317C>T (p.Ala106Val)	not specified [RCV004274630]	uncertain significance	9	127714702	127714702	Human		name
401865690	CV2778891	single nucleotide variant	NM_001002913.3(PTRH1):c.538T>A (p.Phe180Ile)	not specified [RCV004346774]	uncertain significance	9	127714207	127714207	Human		name
405658086	CV3315071	single nucleotide variant	NM_001002913.3(PTRH1):c.302G>A (p.Ser101Asn)	not specified [RCV004438072]	uncertain significance	9	127714989	127714989	Human		name
405658095	CV3315074	single nucleotide variant	NM_001002913.3(PTRH1):c.533G>A (p.Gly178Asp)	not specified [RCV004438075]	uncertain significance	9	127714212	127714212	Human		name
405658098	CV3315075	single nucleotide variant	NM_001002913.3(PTRH1):c.611G>A (p.Arg204His)	not specified [RCV004438076]	uncertain significance	9	127714134	127714134	Human		name
405658100	CV3315076	single nucleotide variant	NM_001002913.3(PTRH1):c.638G>C (p.Gly213Ala)	not specified [RCV004438077]	uncertain significance	9	127714107	127714107	Human		name
407485529	CV3464739	single nucleotide variant	NM_001002913.3(PTRH1):c.494G>T (p.Arg165Leu)	not specified [RCV004662723]	uncertain significance	9	127714251	127714251	Human		name
407486646	CV3464740	single nucleotide variant	NM_001002913.3(PTRH1):c.338C>G (p.Ala113Gly)	not specified [RCV004669280]	uncertain significance	9	127714681	127714681	Human		name
407485537	CV3464742	single nucleotide variant	NM_001002913.3(PTRH1):c.610C>T (p.Arg204Cys)	not specified [RCV004662724]	uncertain significance	9	127714135	127714135	Human		name
597762955	CV3582187	single nucleotide variant	NM_001002913.3(PTRH1):c.457T>G (p.Ser153Ala)	not specified [RCV004849439]	uncertain significance	9	127714384	127714384	Human		name
597762965	CV3582189	single nucleotide variant	NM_001002913.3(PTRH1):c.494G>A (p.Arg165His)	not specified [RCV004849441]	uncertain significance	9	127714251	127714251	Human		name
597762979	CV3582192	single nucleotide variant	NM_001002913.3(PTRH1):c.629C>T (p.Pro210Leu)	not specified [RCV004849444]	uncertain significance	9	127714116	127714116	Human		name
597762985	CV3582193	single nucleotide variant	NM_001002913.3(PTRH1):c.409A>G (p.Ser137Gly)	not specified [RCV004849445]	uncertain significance	9	127714610	127714610	Human		name
597762991	CV3582194	single nucleotide variant	NM_001002913.3(PTRH1):c.626G>A (p.Gly209Glu)	not specified [RCV004849446]	uncertain significance	9	127714119	127714119	Human		name
598250578	CV3901835	single nucleotide variant	NM_001002913.3(PTRH1):c.542C>T (p.Ser181Phe)	not specified [RCV005259078]	uncertain significance	9	127714203	127714203	Human		name
598250585	CV3901836	single nucleotide variant	NM_001002913.3(PTRH1):c.412G>A (p.Ala138Thr)	not specified [RCV005259079]	uncertain significance	9	127714607	127714607	Human		name

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