Zbbx Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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84 records found for search term Zbbx

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8578352	CV112731	single nucleotide variant	NM_001199201.1(ZBBX):c.529-583G>T	Lung cancer [RCV000093254]	uncertain significance	3	167334568	167334568	Human		name
8578348	CV112727	single nucleotide variant	NM_001199201.1(ZBBX):c.2255-8993G>T	Lung cancer [RCV000093250]	uncertain significance	3	167251636	167251636	Human		name
8578350	CV112729	single nucleotide variant	NM_001199201.1(ZBBX):c.1418-3091G>T	Lung cancer [RCV000093252]	uncertain significance	3	167309041	167309041	Human		name
8578351	CV112730	single nucleotide variant	NM_001199201.1(ZBBX):c.1417+2656T>G	Lung cancer [RCV000093253]	uncertain significance	3	167311318	167311318	Human		name
8578349	CV112728	single nucleotide variant	NM_001199201.1(ZBBX):c.2254+13848G>T	Lung cancer [RCV000093251]	uncertain significance	3	167268390	167268390	Human		name
597805323	CV3627525	single nucleotide variant	NM_001199201.2(ZBBX):c.19G>A (p.Val7Ile)	not specified [RCV004882690]	uncertain significance	3	167372883	167372883	Human		name
156081341	CV2368790	single nucleotide variant	NM_001199201.2(ZBBX):c.86G>A (p.Arg29Gln)	not specified [RCV004214666]	uncertain significance	3	167368557	167368557	Human		name
598196281	CV3930224	single nucleotide variant	NM_001199201.2(ZBBX):c.65A>G (p.Tyr22Cys)	not specified [RCV005313491]	uncertain significance	3	167372837	167372837	Human		name
156337361	CV2228678	single nucleotide variant	NM_001199201.2(ZBBX):c.226G>C (p.Val76Leu)	not specified [RCV004092897]	uncertain significance	3	167365933	167365933	Human		name
156144005	CV2268833	single nucleotide variant	NM_001199201.2(ZBBX):c.190G>A (p.Glu64Lys)	not specified [RCV004124210]	uncertain significance	3	167365969	167365969	Human		name
401927573	CV2825049	single nucleotide variant	NM_001199201.2(ZBBX):c.2313A>G (p.Gln771=)	not provided [RCV003439047]	likely benign	3	167242585	167242585	Human		name
405803144	CV3356649	single nucleotide variant	NM_001199201.2(ZBBX):c.104T>C (p.Leu35Ser)	not specified [RCV004478651]	uncertain significance	3	167368539	167368539	Human		name
405803157	CV3356655	single nucleotide variant	NM_001199201.2(ZBBX):c.206C>T (p.Ser69Phe)	not specified [RCV004478657]	uncertain significance	3	167365953	167365953	Human		name
405803161	CV3356657	single nucleotide variant	NM_001199201.2(ZBBX):c.230A>G (p.Asn77Ser)	not specified [RCV004478659]	uncertain significance	3	167365929	167365929	Human		name
597805329	CV3627528	single nucleotide variant	NM_001199201.2(ZBBX):c.149G>A (p.Arg50Gln)	not specified [RCV004882693]	likely benign	3	167368494	167368494	Human		name
156259388	CV2204730	single nucleotide variant	NM_001199201.2(ZBBX):c.880G>A (p.Glu294Lys)	not specified [RCV004074992]	uncertain significance	3	167322220	167322220	Human		name
155977274	CV2218708	single nucleotide variant	NM_001199201.2(ZBBX):c.384G>C (p.Lys128Asn)	not specified [RCV004084638]	uncertain significance	3	167359918	167359918	Human		name
156130279	CV2238603	single nucleotide variant	NM_001199201.2(ZBBX):c.718C>T (p.Arg240Cys)	not specified [RCV004107211]	likely benign	3	167328086	167328086	Human		name
156197195	CV2241602	single nucleotide variant	NM_001199201.2(ZBBX):c.802C>G (p.Gln268Glu)	not specified [RCV004104487]	uncertain significance	3	167328002	167328002	Human		name
156004880	CV2290251	single nucleotide variant	NM_001199201.2(ZBBX):c.947C>T (p.Ser316Phe)	not specified [RCV004152900]	uncertain significance	3	167322153	167322153	Human		name
156202112	CV2300605	single nucleotide variant	NM_001199201.2(ZBBX):c.881A>G (p.Glu294Gly)	not specified [RCV004155563]	uncertain significance	3	167322219	167322219	Human		name
156344749	CV2381910	single nucleotide variant	NM_001199201.2(ZBBX):c.924T>G (p.Ile308Met)	not specified [RCV004225849]	uncertain significance	3	167322176	167322176	Human		name
156249974	CV2394159	single nucleotide variant	NM_001199201.2(ZBBX):c.761A>G (p.Asp254Gly)	not specified [RCV004236357]	uncertain significance	3	167328043	167328043	Human		name
329367866	CV2427618	single nucleotide variant	NM_001199201.2(ZBBX):c.831C>G (p.Asn277Lys)	not specified [RCV004250250]	uncertain significance	3	167327973	167327973	Human		name
329386128	CV2428203	single nucleotide variant	NM_001199201.2(ZBBX):c.439C>T (p.Leu147Phe)	not specified [RCV004251238]	uncertain significance	3	167350509	167350509	Human		name
401724786	CV2693418	single nucleotide variant	NM_001199201.2(ZBBX):c.653C>T (p.Pro218Leu)	not specified [RCV004295369]	uncertain significance	3	167333861	167333861	Human		name
401739762	CV2704706	single nucleotide variant	NM_001199201.2(ZBBX):c.841A>G (p.Asn281Asp)	not specified [RCV004307312]	uncertain significance	3	167327963	167327963	Human		name
401864259	CV2760868	single nucleotide variant	NM_001199201.2(ZBBX):c.416A>G (p.Asn139Ser)	not specified [RCV004336503]	uncertain significance	3	167359886	167359886	Human		name
405803168	CV3356660	single nucleotide variant	NM_001199201.2(ZBBX):c.383A>C (p.Lys128Thr)	not specified [RCV004478662]	uncertain significance	3	167359919	167359919	Human		name
405803170	CV3356661	single nucleotide variant	NM_001199201.2(ZBBX):c.586G>A (p.Val196Ile)	not specified [RCV004478663]	uncertain significance	3	167333928	167333928	Human		name
405803172	CV3356662	single nucleotide variant	NM_001199201.2(ZBBX):c.618T>G (p.Asn206Lys)	not specified [RCV004478664]	uncertain significance	3	167333896	167333896	Human		name
405803174	CV3356663	single nucleotide variant	NM_001199201.2(ZBBX):c.794T>C (p.Val265Ala)	not specified [RCV004478665]	likely benign	3	167328010	167328010	Human		name
407457755	CV3416212	single nucleotide variant	NM_001199201.2(ZBBX):c.863A>T (p.Asp288Val)	not provided [RCV004599090]	uncertain significance	3	167322237	167322237	Human		name
407456683	CV3493934	single nucleotide variant	NM_001199201.2(ZBBX):c.562G>A (p.Val188Ile)	not specified [RCV004686049]	uncertain significance	3	167333952	167333952	Human		name
407456686	CV3493936	single nucleotide variant	NM_001199201.2(ZBBX):c.976C>T (p.His326Tyr)	not specified [RCV004686051]	uncertain significance	3	167322124	167322124	Human		name
407456705	CV3493943	single nucleotide variant	NM_001199201.2(ZBBX):c.811A>C (p.Thr271Pro)	not specified [RCV004686057]	uncertain significance	3	167327993	167327993	Human		name
597805332	CV3627529	single nucleotide variant	NM_001199201.2(ZBBX):c.713C>T (p.Ala238Val)	not specified [RCV004882694]	uncertain significance	3	167328091	167328091	Human		name
597691603	CV3627533	single nucleotide variant	NM_001199201.2(ZBBX):c.486C>G (p.His162Gln)	not specified [RCV004884682]	uncertain significance	3	167350462	167350462	Human		name
598242719	CV3930218	single nucleotide variant	NM_001199201.2(ZBBX):c.353T>C (p.Met118Thr)	not specified [RCV005297163]	uncertain significance	3	167359949	167359949	Human		name
598196271	CV3930219	single nucleotide variant	NM_001199201.2(ZBBX):c.343A>C (p.Asn115His)	not specified [RCV005313489]	uncertain significance	3	167359959	167359959	Human		name
598242738	CV3930222	single nucleotide variant	NM_001199201.2(ZBBX):c.602C>T (p.Pro201Leu)	not specified [RCV005297166]	uncertain significance	3	167333912	167333912	Human		name
15202103	CV720290	single nucleotide variant	NM_001199201.2(ZBBX):c.851C>T (p.Ala284Val)	not provided [RCV000891381]	benign	3	167327953	167327953	Human		name
156089500	CV2202070	single nucleotide variant	NM_001199201.2(ZBBX):c.1804A>G (p.Thr602Ala)	not specified [RCV004075985]	uncertain significance	3	167298380	167298380	Human		name
156139673	CV2250559	single nucleotide variant	NM_001199201.2(ZBBX):c.2315C>T (p.Ser772Leu)	not specified [RCV004129207]	likely benign	3	167242583	167242583	Human		name
156313505	CV2257020	single nucleotide variant	NM_001199201.2(ZBBX):c.1604G>T (p.Arg535Ile)	not specified [RCV004121203]	likely benign	3	167305764	167305764	Human		name
156286446	CV2292083	single nucleotide variant	NM_001199201.2(ZBBX):c.1179A>G (p.Ile393Met)	not specified [RCV004160352]	uncertain significance	3	167317020	167317020	Human		name
156209796	CV2304584	single nucleotide variant	NM_001199201.2(ZBBX):c.1929T>A (p.Asn643Lys)	not specified [RCV004166479]	uncertain significance	3	167288934	167288934	Human		name
156103653	CV2310784	single nucleotide variant	NM_001199201.2(ZBBX):c.2323A>G (p.Ile775Val)	not specified [RCV004157709]	uncertain significance	3	167242575	167242575	Human		name
156395765	CV2325919	single nucleotide variant	NM_001199201.2(ZBBX):c.1880A>G (p.Glu627Gly)	not specified [RCV004174094]	likely benign	3	167288983	167288983	Human		name
156325724	CV2335350	single nucleotide variant	NM_001199201.2(ZBBX):c.1112A>G (p.Gln371Arg)	not specified [RCV004186908]	uncertain significance	3	167317087	167317087	Human		name
155985889	CV2345432	single nucleotide variant	NM_001199201.2(ZBBX):c.1580A>C (p.Glu527Ala)	not specified [RCV004198207]	uncertain significance	3	167305788	167305788	Human		name
156346247	CV2373042	single nucleotide variant	NM_001199201.2(ZBBX):c.2264A>G (p.Glu755Gly)	not specified [RCV004224068]	uncertain significance	3	167242634	167242634	Human		name
156031132	CV2380947	single nucleotide variant	NM_001199201.2(ZBBX):c.2001G>T (p.Gln667His)	not specified [RCV004220527]	uncertain significance	3	167282491	167282491	Human		name
156347936	CV2383010	single nucleotide variant	NM_001199201.2(ZBBX):c.2362G>C (p.Val788Leu)	not specified [RCV004217595]	uncertain significance	3	167242536	167242536	Human		name
156085667	CV2390666	single nucleotide variant	NM_001199201.2(ZBBX):c.1450G>A (p.Val484Met)	not specified [RCV004239184]	uncertain significance	3	167305918	167305918	Human		name
329390771	CV2455455	single nucleotide variant	NM_001199201.2(ZBBX):c.1313A>G (p.Tyr438Cys)	not specified [RCV004276727]	uncertain significance	3	167314078	167314078	Human		name
329381775	CV2467360	single nucleotide variant	NM_001199201.2(ZBBX):c.1310C>T (p.Pro437Leu)	not specified [RCV004285148]	likely benign	3	167314081	167314081	Human		name
401719602	CV2701191	single nucleotide variant	NM_001199201.2(ZBBX):c.1570G>A (p.Val524Ile)	not specified [RCV004309767]	likely benign	3	167305798	167305798	Human		name
401740218	CV2705920	single nucleotide variant	NM_001199201.2(ZBBX):c.2457G>T (p.Glu819Asp)	not specified [RCV004320848]	likely benign	3	167240856	167240856	Human		name
405803146	CV3356650	single nucleotide variant	NM_001199201.2(ZBBX):c.1431C>G (p.Asn477Lys)	not specified [RCV004478652]	uncertain significance	3	167305937	167305937	Human		name
405803148	CV3356651	single nucleotide variant	NM_001199201.2(ZBBX):c.1568G>A (p.Cys523Tyr)	not specified [RCV004478653]	uncertain significance	3	167305800	167305800	Human		name
405803151	CV3356652	single nucleotide variant	NM_001199201.2(ZBBX):c.1594T>G (p.Leu532Val)	not specified [RCV004478654]	uncertain significance	3	167305774	167305774	Human		name
405803153	CV3356653	single nucleotide variant	NM_001199201.2(ZBBX):c.1648A>G (p.Ile550Val)	not specified [RCV004478655]	uncertain significance	3	167305720	167305720	Human		name
405803159	CV3356656	single nucleotide variant	NM_001199201.2(ZBBX):c.2204A>G (p.His735Arg)	not specified [RCV004478658]	uncertain significance	3	167282288	167282288	Human		name
405803164	CV3356658	single nucleotide variant	NM_001199201.2(ZBBX):c.2386G>A (p.Glu796Lys)	not specified [RCV004478660]	uncertain significance	3	167242512	167242512	Human		name
405803166	CV3356659	single nucleotide variant	NM_001199201.2(ZBBX):c.2432C>T (p.Ser811Leu)	not specified [RCV004478661]	uncertain significance	3	167240881	167240881	Human		name
407456689	CV3493937	single nucleotide variant	NM_001199201.2(ZBBX):c.1064C>T (p.Ser355Phe)	not specified [RCV004686052]	uncertain significance	3	167317517	167317517	Human		name
407456693	CV3493938	single nucleotide variant	NM_001199201.2(ZBBX):c.2083C>T (p.Pro695Ser)	not specified [RCV004686053]	uncertain significance	3	167282409	167282409	Human		name
407456695	CV3493939	single nucleotide variant	NM_001199201.2(ZBBX):c.2145T>G (p.Ile715Met)	not specified [RCV004686054]	uncertain significance	3	167282347	167282347	Human		name
407456698	CV3493940	single nucleotide variant	NM_001199201.2(ZBBX):c.1055C>T (p.Ala352Val)	not specified [RCV004686055]	likely benign	3	167317526	167317526	Human		name
407465825	CV3493941	single nucleotide variant	NM_001199201.2(ZBBX):c.1172T>C (p.Leu391Pro)	not specified [RCV004688872]	uncertain significance	3	167317027	167317027	Human		name
407456702	CV3493942	single nucleotide variant	NM_001199201.2(ZBBX):c.1469C>G (p.Ser490Cys)	not specified [RCV004686056]	uncertain significance	3	167305899	167305899	Human		name
407456709	CV3493944	single nucleotide variant	NM_001199201.2(ZBBX):c.2097T>G (p.Ser699Arg)	not specified [RCV004686058]	uncertain significance	3	167282395	167282395	Human		name
597805325	CV3627526	single nucleotide variant	NM_001199201.2(ZBBX):c.1554G>T (p.Lys518Asn)	not specified [RCV004882691]	uncertain significance	3	167305814	167305814	Human		name
597805327	CV3627527	single nucleotide variant	NM_001199201.2(ZBBX):c.1135G>T (p.Val379Leu)	not specified [RCV004882692]	uncertain significance	3	167317064	167317064	Human		name
597691572	CV3627530	single nucleotide variant	NM_001199201.2(ZBBX):c.1193A>T (p.Asp398Val)	not specified [RCV004884679]	uncertain significance	3	167317006	167317006	Human		name
597691591	CV3627532	single nucleotide variant	NM_001199201.2(ZBBX):c.1241A>T (p.Lys414Ile)	not specified [RCV004884681]	uncertain significance	3	167315783	167315783	Human		name
598242725	CV3930220	single nucleotide variant	NM_001199201.2(ZBBX):c.1149C>A (p.Asn383Lys)	not specified [RCV005297164]	uncertain significance	3	167317050	167317050	Human		name
598242732	CV3930221	single nucleotide variant	NM_001199201.2(ZBBX):c.1765A>G (p.Lys589Glu)	not specified [RCV005297165]	likely benign	3	167298419	167298419	Human		name
598196276	CV3930223	single nucleotide variant	NM_001199201.2(ZBBX):c.1778G>C (p.Gly593Ala)	not specified [RCV005313490]	uncertain significance	3	167298406	167298406	Human		name
598242743	CV3930225	single nucleotide variant	NM_001199201.2(ZBBX):c.1670G>A (p.Ser557Asn)	not specified [RCV005297167]	uncertain significance	3	167305698	167305698	Human		name
598196286	CV3930226	single nucleotide variant	NM_001199201.2(ZBBX):c.1835A>T (p.His612Leu)	not specified [RCV005313492]	uncertain significance	3	167298349	167298349	Human		name
15103256	CV720288	single nucleotide variant	NM_001199201.2(ZBBX):c.1078G>A (p.Asp360Asn)	not provided [RCV000892636]	benign	3	167317503	167317503	Human		name
15202099	CV720289	single nucleotide variant	NM_001199201.2(ZBBX):c.1015C>T (p.Pro339Ser)	not provided [RCV000891380]	benign	3	167317566	167317566	Human		name

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