Tex10 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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82 records found for search term Tex10

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156341764	CV2368456	single nucleotide variant	NM_017746.4(TEX10):c.19C>T (p.Arg7Cys)	not specified [RCV004219219]	uncertain significance	9	100349345	100349345	Human		name
156337222	CV2343024	single nucleotide variant	NM_017746.4(TEX10):c.85A>G (p.Thr29Ala)	not specified [RCV004192626]	uncertain significance	9	100349279	100349279	Human		name
597750514	CV3619619	single nucleotide variant	NM_017746.4(TEX10):c.91A>G (p.Thr31Ala)	not specified [RCV004866725]	uncertain significance	9	100349273	100349273	Human		name
597750556	CV3619627	single nucleotide variant	NM_017746.4(TEX10):c.28G>C (p.Asp10His)	not specified [RCV004866733]	uncertain significance	9	100349336	100349336	Human		name
405781992	CV3342443	single nucleotide variant	NM_017746.4(TEX10):c.130C>T (p.Leu44Phe)	not specified [RCV004472119]	uncertain significance	9	100349234	100349234	Human		name
407519889	CV3482464	single nucleotide variant	NM_017746.4(TEX10):c.106A>G (p.Lys36Glu)	not specified [RCV004676739]	uncertain significance	9	100349258	100349258	Human		name
598165451	CV3916900	single nucleotide variant	NM_017746.4(TEX10):c.1341G>A (p.Ala447=)	not specified [RCV005283454]	likely benign	9	100330079	100330079	Human		name
598226530	CV3916901	single nucleotide variant	NM_017746.4(TEX10):c.245A>C (p.Lys82Thr)	not specified [RCV005294441]	uncertain significance	9	100347342	100347342	Human		name
598226545	CV3916903	single nucleotide variant	NM_017746.4(TEX10):c.199C>G (p.His67Asp)	not specified [RCV005294443]	uncertain significance	9	100347388	100347388	Human		name
156072587	CV2295974	single nucleotide variant	NM_017746.4(TEX10):c.659C>T (p.Ser220Phe)	not specified [RCV004151866]	uncertain significance	9	100346928	100346928	Human		name
156281847	CV2338494	single nucleotide variant	NM_017746.4(TEX10):c.835A>G (p.Ile279Val)	not specified [RCV004188533]	uncertain significance	9	100346752	100346752	Human		name
156402487	CV2361514	single nucleotide variant	NM_017746.4(TEX10):c.394G>C (p.Glu132Gln)	not specified [RCV004221151]	uncertain significance	9	100347193	100347193	Human		name
155994369	CV2377488	single nucleotide variant	NM_017746.4(TEX10):c.840G>C (p.Gln280His)	not specified [RCV004225655]	uncertain significance	9	100346747	100346747	Human		name
329366100	CV2438099	single nucleotide variant	NM_017746.4(TEX10):c.307G>A (p.Val103Met)	not specified [RCV004256883]	uncertain significance	9	100347280	100347280	Human		name
401885055	CV2771170	single nucleotide variant	NM_017746.4(TEX10):c.796T>C (p.Phe266Leu)	not specified [RCV004346164]	uncertain significance	9	100346791	100346791	Human		name
405782025	CV3342449	single nucleotide variant	NM_017746.4(TEX10):c.306A>C (p.Glu102Asp)	not specified [RCV004472125]	uncertain significance	9	100347281	100347281	Human		name
405782032	CV3342450	single nucleotide variant	NM_017746.4(TEX10):c.359A>G (p.Gln120Arg)	not specified [RCV004472126]	uncertain significance	9	100347228	100347228	Human		name
405782037	CV3342451	single nucleotide variant	NM_017746.4(TEX10):c.817G>A (p.Ala273Thr)	not specified [RCV004472127]	uncertain significance	9	100346770	100346770	Human		name
597750542	CV3619624	single nucleotide variant	NM_017746.4(TEX10):c.369A>T (p.Gln123His)	not specified [RCV004866730]	uncertain significance	9	100347218	100347218	Human		name
597750560	CV3619628	single nucleotide variant	NM_017746.4(TEX10):c.334G>A (p.Ala112Thr)	not specified [RCV004866734]	uncertain significance	9	100347253	100347253	Human		name
597750566	CV3619629	single nucleotide variant	NM_017746.4(TEX10):c.607G>A (p.Asp203Asn)	not specified [RCV004866735]	uncertain significance	9	100346980	100346980	Human		name
155917210	CV2202261	single nucleotide variant	NM_017746.4(TEX10):c.1439A>G (p.Asn480Ser)	not specified [RCV004078199]	uncertain significance	9	100329981	100329981	Human		name
156254714	CV2203298	single nucleotide variant	NM_017746.4(TEX10):c.2031T>A (p.Asp677Glu)	not specified [RCV004071329]	uncertain significance	9	100321720	100321720	Human		name
155919303	CV2254842	single nucleotide variant	NM_017746.4(TEX10):c.1588A>C (p.Ile530Leu)	not specified [RCV004115303]	uncertain significance	9	100329177	100329177	Human		name
155992551	CV2255849	single nucleotide variant	NM_017746.4(TEX10):c.1946T>G (p.Leu649Trp)	not specified [RCV004122008]	uncertain significance	9	100326335	100326335	Human		name
156359049	CV2260951	single nucleotide variant	NM_017746.4(TEX10):c.2206G>A (p.Val736Ile)	not specified [RCV004125834]	uncertain significance	9	100310376	100310376	Human		name
156364012	CV2262754	single nucleotide variant	NM_017746.4(TEX10):c.2548A>G (p.Asn850Asp)	not specified [RCV004130933]	uncertain significance	9	100303760	100303760	Human		name
156062497	CV2263212	single nucleotide variant	NM_017746.4(TEX10):c.2744T>C (p.Ile915Thr)	not specified [RCV004131438]	uncertain significance	9	100302237	100302237	Human		name
155918171	CV2283491	single nucleotide variant	NM_017746.4(TEX10):c.2111G>A (p.Gly704Glu)	not specified [RCV004139708]	uncertain significance	9	100320356	100320356	Human		name
156254038	CV2284122	single nucleotide variant	NM_017746.4(TEX10):c.1265C>T (p.Thr422Ile)	not specified [RCV004144716]	uncertain significance	9	100330155	100330155	Human		name
156210882	CV2309855	single nucleotide variant	NM_017746.4(TEX10):c.2269A>G (p.Ile757Val)	not specified [RCV004160964]	uncertain significance	9	100310313	100310313	Human		name
156244708	CV2313230	single nucleotide variant	NM_017746.4(TEX10):c.1565T>C (p.Leu522Ser)	not specified [RCV004161482]	uncertain significance	9	100329200	100329200	Human		name
156300517	CV2322499	single nucleotide variant	NM_017746.4(TEX10):c.2677A>G (p.Thr893Ala)	not specified [RCV004180620]	uncertain significance	9	100302304	100302304	Human		name
156088929	CV2392013	single nucleotide variant	NM_017746.4(TEX10):c.1496C>T (p.Thr499Ile)	not specified [RCV004235869]	uncertain significance	9	100329269	100329269	Human		name
156253833	CV2397476	single nucleotide variant	NM_017746.4(TEX10):c.2429C>G (p.Thr810Ser)	not specified [RCV004236951]	uncertain significance	9	100308536	100308536	Human		name
401778186	CV2700666	single nucleotide variant	NM_017746.4(TEX10):c.1169A>C (p.Asp390Ala)	not specified [RCV004313383]	uncertain significance	9	100340338	100340338	Human		name
401897856	CV2773028	single nucleotide variant	NM_017746.4(TEX10):c.1190G>A (p.Ser397Asn)	not specified [RCV004351476]	uncertain significance	9	100340317	100340317	Human		name
401892408	CV2785406	single nucleotide variant	NM_017746.4(TEX10):c.1772G>A (p.Ser591Asn)	not specified [RCV004357143]	uncertain significance	9	100327816	100327816	Human		name
405781987	CV3342442	single nucleotide variant	NM_017746.4(TEX10):c.1033G>C (p.Gly345Arg)	not specified [RCV004472118]	uncertain significance	9	100346176	100346176	Human		name
405781998	CV3342444	single nucleotide variant	NM_017746.4(TEX10):c.1415C>G (p.Ser472Cys)	not specified [RCV004472120]	uncertain significance	9	100330005	100330005	Human		name
405782002	CV3342445	single nucleotide variant	NM_017746.4(TEX10):c.1648C>T (p.Arg550Cys)	not specified [RCV004472121]	uncertain significance	9	100327940	100327940	Human		name
405782007	CV3342446	single nucleotide variant	NM_017746.4(TEX10):c.2527A>G (p.Met843Val)	not specified [RCV004472122]	uncertain significance	9	100303781	100303781	Human		name
405782012	CV3342447	single nucleotide variant	NM_017746.4(TEX10):c.2557G>A (p.Gly853Arg)	not specified [RCV004472123]	uncertain significance	9	100303751	100303751	Human		name
405782018	CV3342448	single nucleotide variant	NM_017746.4(TEX10):c.2626C>T (p.His876Tyr)	not specified [RCV004472124]	uncertain significance	9	100303682	100303682	Human		name
407519884	CV3482462	single nucleotide variant	NM_017746.4(TEX10):c.1831C>T (p.Pro611Ser)	not specified [RCV004676737]	uncertain significance	9	100326450	100326450	Human		name
407519887	CV3482463	single nucleotide variant	NM_017746.4(TEX10):c.1726A>G (p.Ile576Val)	not specified [RCV004676738]	uncertain significance	9	100327862	100327862	Human		name
407518501	CV3482465	single nucleotide variant	NM_017746.4(TEX10):c.1943G>A (p.Ser648Asn)	not specified [RCV004675998]	uncertain significance	9	100326338	100326338	Human		name
407518504	CV3482466	single nucleotide variant	NM_017746.4(TEX10):c.1973A>G (p.His658Arg)	not specified [RCV004675999]	uncertain significance	9	100326308	100326308	Human		name
597750504	CV3619617	single nucleotide variant	NM_017746.4(TEX10):c.2441G>A (p.Gly814Glu)	not specified [RCV004866723]	uncertain significance	9	100308524	100308524	Human		name
597750509	CV3619618	single nucleotide variant	NM_017746.4(TEX10):c.1951G>A (p.Ala651Thr)	not specified [RCV004866724]	uncertain significance	9	100326330	100326330	Human		name
597750519	CV3619620	single nucleotide variant	NM_017746.4(TEX10):c.2701G>C (p.Glu901Gln)	not specified [RCV004866726]	uncertain significance	9	100302280	100302280	Human		name
597750526	CV3619621	single nucleotide variant	NM_017746.4(TEX10):c.2655G>T (p.Gln885His)	not specified [RCV004866727]	uncertain significance	9	100303653	100303653	Human		name
597750532	CV3619622	single nucleotide variant	NM_017746.4(TEX10):c.1256A>G (p.Lys419Arg)	not specified [RCV004866728]	uncertain significance	9	100330164	100330164	Human		name
597750546	CV3619625	single nucleotide variant	NM_017746.4(TEX10):c.1861C>A (p.Leu621Ile)	not specified [RCV004866731]	uncertain significance	9	100326420	100326420	Human		name
597750551	CV3619626	single nucleotide variant	NM_017746.4(TEX10):c.1531C>A (p.Gln511Lys)	not specified [RCV004866732]	uncertain significance	9	100329234	100329234	Human		name
598165445	CV3916899	single nucleotide variant	NM_017746.4(TEX10):c.2108G>A (p.Arg703Gln)	not specified [RCV005283453]	uncertain significance	9	100320359	100320359	Human		name
598226539	CV3916902	single nucleotide variant	NM_017746.4(TEX10):c.1946T>C (p.Leu649Ser)	not specified [RCV005294442]	uncertain significance	9	100326335	100326335	Human		name
8626622	CV81766	single nucleotide variant	NM_001161584.1(TEX10):c.2594C>T (p.Ala865Val)	Malignant melanoma [RCV000061844]	not provided	9	100303666	100303666	Human		name
8586156	CV120752	single nucleotide variant	NM_031451.4(TEX101):c.15+344T>G	Lung cancer [RCV000101272]	uncertain significance	19	43406863	43406863	Human		name
597750611	CV3619639	single nucleotide variant	NM_001130011.3(TEX101):c.17T>A (p.Ile6Asn)	not specified [RCV004866744]	uncertain significance	19	43415936	43415936	Human		name
156061264	CV2263115	single nucleotide variant	NM_001130011.3(TEX101):c.92G>A (p.Gly31Asp)	not specified [RCV004131357]	uncertain significance	19	43416126	43416126	Human		name
401739187	CV2708358	single nucleotide variant	NM_001130011.3(TEX101):c.86A>T (p.Gln29Leu)	not specified [RCV004313476]	uncertain significance	19	43416120	43416120	Human		name
597795039	CV3619637	single nucleotide variant	NM_001130011.3(TEX101):c.97T>C (p.Ser33Pro)	not specified [RCV004878055]	uncertain significance	19	43416131	43416131	Human		name
401890761	CV2778948	single nucleotide variant	NM_001130011.3(TEX101):c.209G>T (p.Gly70Val)	not specified [RCV004348611]	uncertain significance	19	43416373	43416373	Human		name
597750576	CV3619631	single nucleotide variant	NM_001130011.3(TEX101):c.262G>A (p.Ala88Thr)	not specified [RCV004866737]	uncertain significance	19	43416426	43416426	Human		name
597750616	CV3619640	single nucleotide variant	NM_001130011.3(TEX101):c.167A>G (p.Lys56Arg)	not specified [RCV004866745]	uncertain significance	19	43416201	43416201	Human		name
598226551	CV3916905	single nucleotide variant	NM_001130011.3(TEX101):c.295G>A (p.Gly99Ser)	not specified [RCV005294444]	uncertain significance	19	43416459	43416459	Human		name
156130794	CV2235186	single nucleotide variant	NM_001130011.3(TEX101):c.581T>G (p.Met194Arg)	not specified [RCV004107241]	uncertain significance	19	43418228	43418228	Human		name
156113142	CV2261285	single nucleotide variant	NM_001130011.3(TEX101):c.688C>T (p.Pro230Ser)	not specified [RCV004128151]	likely benign	19	43418335	43418335	Human		name
156086695	CV2289983	single nucleotide variant	NM_001130011.3(TEX101):c.634C>G (p.Gln212Glu)	not specified [RCV004150630]	uncertain significance	19	43418281	43418281	Human		name
156048110	CV2315744	single nucleotide variant	NM_001130011.3(TEX101):c.488G>A (p.Arg163Gln)	not specified [RCV004169753]	uncertain significance	19	43417974	43417974	Human		name
156151379	CV2318776	single nucleotide variant	NM_001130011.3(TEX101):c.743T>C (p.Phe248Ser)	not specified [RCV004175696]	uncertain significance	19	43418390	43418390	Human		name
155910256	CV2369806	single nucleotide variant	NM_001130011.3(TEX101):c.323A>G (p.Tyr108Cys)	not specified [RCV004215193]	uncertain significance	19	43416487	43416487	Human		name
405782048	CV3342453	single nucleotide variant	NM_001130011.3(TEX101):c.566T>C (p.Ile189Thr)	not specified [RCV004472129]	uncertain significance	19	43418213	43418213	Human		name
405782053	CV3342454	single nucleotide variant	NM_001130011.3(TEX101):c.673A>G (p.Thr225Ala)	not specified [RCV004472130]	uncertain significance	19	43418320	43418320	Human		name
597750571	CV3619630	single nucleotide variant	NM_001130011.3(TEX101):c.623C>T (p.Ala208Val)	not specified [RCV004866736]	likely benign	19	43418270	43418270	Human		name
597750580	CV3619632	single nucleotide variant	NM_001130011.3(TEX101):c.308C>A (p.Thr103Asn)	not specified [RCV004866738]	uncertain significance	19	43416472	43416472	Human		name
597750590	CV3619634	single nucleotide variant	NM_001130011.3(TEX101):c.310T>C (p.Ser104Pro)	not specified [RCV004866740]	uncertain significance	19	43416474	43416474	Human		name
597750596	CV3619635	single nucleotide variant	NM_001130011.3(TEX101):c.647A>G (p.Gln216Arg)	not specified [RCV004866741]	uncertain significance	19	43418294	43418294	Human		name
597750601	CV3619636	single nucleotide variant	NM_001130011.3(TEX101):c.476A>G (p.Asn159Ser)	not specified [RCV004866742]	uncertain significance	19	43417962	43417962	Human		name
597750606	CV3619638	single nucleotide variant	NM_001130011.3(TEX101):c.354C>G (p.Asp118Glu)	not specified [RCV004866743]	likely benign	19	43416518	43416518	Human		name
598165464	CV3916906	single nucleotide variant	NM_001130011.3(TEX101):c.613G>A (p.Val205Met)	not specified [RCV005283456]	uncertain significance	19	43418260	43418260	Human		name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

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InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

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