Tor2a Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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49 records found for search term Tor2a

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401918456	CV2826405	single nucleotide variant	NM_001085347.3(TOR2A):c.593+160G>A	not provided [RCV003430253]	likely benign	9	127733225	127733225	Human		name
156398395	CV2200748	single nucleotide variant	NM_001085347.3(TOR2A):c.62T>C (p.Val21Ala)	not specified [RCV004081396]	uncertain significance	9	127735209	127735209	Human		name
401893061	CV2758440	single nucleotide variant	NM_001085347.3(TOR2A):c.765C>T (p.Asp255=)	not specified [RCV004335093]	likely benign	9	127732235	127732235	Human		name
405758237	CV3347084	single nucleotide variant	NM_001085347.3(TOR2A):c.801C>T (p.His267=)	not specified [RCV004468184]	likely benign	9	127732199	127732199	Human		name
407521047	CV3486832	single nucleotide variant	NM_001085347.3(TOR2A):c.825G>A (p.Glu275=)	not specified [RCV004677159]	likely benign	9	127732175	127732175	Human		name
407461135	CV3486833	single nucleotide variant	NM_001085347.3(TOR2A):c.813C>T (p.Cys271=)	not specified [RCV004687576]	likely benign	9	127732187	127732187	Human		name
597787023	CV3611041	single nucleotide variant	NM_001085347.3(TOR2A):c.480C>T (p.Phe160=)	not specified [RCV004875519]	likely benign	9	127733498	127733498	Human		name
597787042	CV3611046	single nucleotide variant	NM_001085347.3(TOR2A):c.37T>G (p.Ser13Ala)	not specified [RCV004875524]	uncertain significance	9	127735234	127735234	Human		name
597787045	CV3611047	single nucleotide variant	NM_001085347.3(TOR2A):c.462C>T (p.Gly154=)	not specified [RCV004875525]	likely benign	9	127733516	127733516	Human		name
598188495	CV3928166	single nucleotide variant	NM_001085347.3(TOR2A):c.777C>A (p.Pro259=)	not specified [RCV005287947]	likely benign	9	127732223	127732223	Human		name
155981138	CV2212194	single nucleotide variant	NM_001085347.3(TOR2A):c.247C>T (p.Pro83Ser)	not specified [RCV004089085]	uncertain significance	9	127734469	127734469	Human		name
156395761	CV2325914	single nucleotide variant	NM_001085347.3(TOR2A):c.194T>C (p.Leu65Pro)	not specified [RCV004174089]	uncertain significance	9	127734522	127734522	Human		name
405758187	CV3347076	single nucleotide variant	NM_001085347.3(TOR2A):c.173A>G (p.Gln58Arg)	not specified [RCV004468176]	uncertain significance	9	127734543	127734543	Human		name
405758193	CV3347077	single nucleotide variant	NM_001085347.3(TOR2A):c.193C>A (p.Leu65Met)	not specified [RCV004468177]	uncertain significance	9	127734523	127734523	Human		name
156317095	CV2203905	single nucleotide variant	NM_001085347.3(TOR2A):c.937G>A (p.Val313Met)	not specified [RCV004069956]	uncertain significance	9	127732063	127732063	Human		name
156379229	CV2207917	single nucleotide variant	NM_001085347.3(TOR2A):c.925G>A (p.Gly309Ser)	not specified [RCV004084338]	uncertain significance	9	127732075	127732075	Human		name
156401054	CV2213794	single nucleotide variant	NM_001085347.3(TOR2A):c.656G>C (p.Arg219Pro)	not specified [RCV004089854]	uncertain significance	9	127732629	127732629	Human		name
156249828	CV2222156	single nucleotide variant	NM_001085347.3(TOR2A):c.734A>G (p.Asn245Ser)	not specified [RCV004104909]	uncertain significance	9	127732266	127732266	Human		name
156157316	CV2262390	single nucleotide variant	NM_001085347.3(TOR2A):c.737C>T (p.Ser246Leu)	not specified [RCV004128838]	uncertain significance	9	127732263	127732263	Human		name
156307757	CV2312420	single nucleotide variant	NM_001085347.3(TOR2A):c.553T>C (p.Tyr185His)	not specified [RCV004167107]	uncertain significance	9	127733425	127733425	Human		name
156332505	CV2339791	single nucleotide variant	NM_001085347.3(TOR2A):c.646C>T (p.Arg216Trp)	not specified [RCV004196486]	uncertain significance	9	127732639	127732639	Human		name
156241745	CV2346943	single nucleotide variant	NM_001085347.3(TOR2A):c.785C>G (p.Pro262Arg)	not specified [RCV004202390]	uncertain significance	9	127732215	127732215	Human		name
156171978	CV2400738	single nucleotide variant	NM_001085347.3(TOR2A):c.463C>T (p.Arg155Cys)	not specified [RCV004242406]	uncertain significance	9	127733515	127733515	Human		name
329373622	CV2434554	single nucleotide variant	NM_001085347.3(TOR2A):c.697C>T (p.Arg233Cys)	not specified [RCV004254255]	uncertain significance	9	127732588	127732588	Human		name
329400533	CV2438453	single nucleotide variant	NM_001085347.3(TOR2A):c.338G>A (p.Gly113Asp)	not specified [RCV004259603]	uncertain significance	9	127734378	127734378	Human		name
401745934	CV2678735	single nucleotide variant	NM_001085347.3(TOR2A):c.423T>A (p.Asp141Glu)	not specified [RCV004292731]	uncertain significance	9	127733555	127733555	Human		name
401724282	CV2681368	single nucleotide variant	NM_001085347.3(TOR2A):c.805C>T (p.Arg269Trp)	not specified [RCV004291915]	uncertain significance	9	127732195	127732195	Human		name
401757943	CV2731568	single nucleotide variant	NM_001085347.3(TOR2A):c.766G>A (p.Ala256Thr)	not specified [RCV004330914]	uncertain significance	9	127732234	127732234	Human		name
405758199	CV3347078	single nucleotide variant	NM_001085347.3(TOR2A):c.356G>A (p.Arg119His)	not specified [RCV004468178]	likely benign	9	127734360	127734360	Human		name
405758205	CV3347079	single nucleotide variant	NM_001085347.3(TOR2A):c.362A>G (p.His121Arg)	not specified [RCV004468179]	uncertain significance	9	127734354	127734354	Human		name
405758212	CV3347080	single nucleotide variant	NM_001085347.3(TOR2A):c.376G>A (p.Val126Ile)	not specified [RCV004468180]	uncertain significance	9	127734340	127734340	Human		name
405758215	CV3347081	single nucleotide variant	NM_001085347.3(TOR2A):c.608A>C (p.Lys203Thr)	not specified [RCV004468181]	uncertain significance	9	127732677	127732677	Human		name
405758222	CV3347082	single nucleotide variant	NM_001085347.3(TOR2A):c.679C>G (p.Leu227Val)	not specified [RCV004468182]	uncertain significance	9	127732606	127732606	Human		name
405758244	CV3347085	single nucleotide variant	NM_001085347.3(TOR2A):c.958T>C (p.Phe320Leu)	not specified [RCV004468185]	uncertain significance	9	127732042	127732042	Human		name
407521040	CV3486830	single nucleotide variant	NM_001085347.3(TOR2A):c.944C>T (p.Ser315Phe)	not specified [RCV004677157]	uncertain significance	9	127732056	127732056	Human		name
407521051	CV3486834	single nucleotide variant	NM_001085347.3(TOR2A):c.623T>C (p.Val208Ala)	not specified [RCV004677160]	uncertain significance	9	127732662	127732662	Human		name
597787011	CV3611038	single nucleotide variant	NM_001085347.3(TOR2A):c.308G>T (p.Ser103Ile)	not specified [RCV004875516]	uncertain significance	9	127734408	127734408	Human		name
597787015	CV3611039	single nucleotide variant	NM_001085347.3(TOR2A):c.599C>T (p.Thr200Met)	not specified [RCV004875517]	uncertain significance	9	127732686	127732686	Human		name
597787019	CV3611040	single nucleotide variant	NM_001085347.3(TOR2A):c.785C>T (p.Pro262Leu)	not specified [RCV004875518]	uncertain significance	9	127732215	127732215	Human		name
597787026	CV3611042	single nucleotide variant	NM_001085347.3(TOR2A):c.628T>A (p.Leu210Met)	not specified [RCV004875520]	uncertain significance	9	127732657	127732657	Human		name
597787034	CV3611044	single nucleotide variant	NM_001085347.3(TOR2A):c.947G>A (p.Arg316Gln)	not specified [RCV004875522]	uncertain significance	9	127732053	127732053	Human		name
597787038	CV3611045	single nucleotide variant	NM_001085347.3(TOR2A):c.745A>G (p.Met249Val)	not specified [RCV004875523]	uncertain significance	9	127732255	127732255	Human		name
597787049	CV3611048	single nucleotide variant	NM_001085347.3(TOR2A):c.421G>A (p.Asp141Asn)	not specified [RCV004875526]	uncertain significance	9	127733557	127733557	Human		name
598188486	CV3928164	single nucleotide variant	NM_001085347.3(TOR2A):c.635C>T (p.Ala212Val)	not specified [RCV005287946]	uncertain significance	9	127732650	127732650	Human		name
598254651	CV3928165	single nucleotide variant	NM_001085347.3(TOR2A):c.498G>A (p.Met166Ile)	not specified [RCV005278478]	uncertain significance	9	127733480	127733480	Human		name
598254658	CV3928167	single nucleotide variant	NM_001085347.3(TOR2A):c.952G>A (p.Ala318Thr)	not specified [RCV005278479]	likely benign	9	127732048	127732048	Human		name
598254665	CV3928168	single nucleotide variant	NM_001085347.3(TOR2A):c.610C>G (p.Gln204Glu)	not specified [RCV005278480]	uncertain significance	9	127732675	127732675	Human		name
598254672	CV3928169	single nucleotide variant	NM_001085347.3(TOR2A):c.556G>C (p.Gly186Arg)	not specified [RCV005278481]	uncertain significance	9	127733422	127733422	Human		name
15127148	CV736887	single nucleotide variant	NM_001085347.3(TOR2A):c.907C>A (p.Gln303Lys)	not provided [RCV000897056]	benign	9	127732093	127732093	Human		name

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