Zbtb39 Variant Search Result - Rat Genome Database

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65 records found for search term Zbtb39

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
597693181	CV3624331	single nucleotide variant	NM_014830.3(ZBTB39):c.93C>G (p.Asp31Glu)	not specified [RCV004884855]	uncertain significance	12	57004825	57004825	Human		name
156299072	CV2310690	single nucleotide variant	NM_014830.3(ZBTB39):c.265A>T (p.Thr89Ser)	not specified [RCV004157345]	uncertain significance	12	57004653	57004653	Human		name
8634806	CV90026	single nucleotide variant	NM_014830.2(ZBTB39):c.1392C>T (p.Phe464=)	Malignant melanoma [RCV000070123]	not provided	12	57003526	57003526	Human		name
156248083	CV2203039	single nucleotide variant	NM_014830.3(ZBTB39):c.752G>A (p.Ser251Asn)	not specified [RCV004069291]	uncertain significance	12	57004166	57004166	Human		name
156146127	CV2218877	single nucleotide variant	NM_014830.3(ZBTB39):c.479G>T (p.Arg160Leu)	not specified [RCV004085111]	uncertain significance	12	57004439	57004439	Human		name
156069798	CV2271008	single nucleotide variant	NM_014830.3(ZBTB39):c.502G>T (p.Ala168Ser)	not specified [RCV004133822]	uncertain significance	12	57004416	57004416	Human		name
156079898	CV2292642	single nucleotide variant	NM_014830.3(ZBTB39):c.848C>T (p.Ser283Phe)	not specified [RCV004154330]	uncertain significance	12	57004070	57004070	Human		name
156085138	CV2331046	single nucleotide variant	NM_014830.3(ZBTB39):c.722C>T (p.Thr241Met)	not specified [RCV004188084]	uncertain significance	12	57004196	57004196	Human		name
155927151	CV2345347	single nucleotide variant	NM_014830.3(ZBTB39):c.508A>G (p.Arg170Gly)	not specified [RCV004198127]	uncertain significance	12	57004410	57004410	Human		name
156069555	CV2381248	single nucleotide variant	NM_014830.3(ZBTB39):c.670A>C (p.Met224Leu)	not specified [RCV004227313]	uncertain significance	12	57004248	57004248	Human		name
155956434	CV2387288	single nucleotide variant	NM_014830.3(ZBTB39):c.359C>T (p.Ser120Phe)	not specified [RCV004238377]	uncertain significance	12	57004559	57004559	Human		name
329390852	CV2455540	single nucleotide variant	NM_014830.3(ZBTB39):c.731G>T (p.Cys244Phe)	not specified [RCV004276798]	uncertain significance	12	57004187	57004187	Human		name
401739224	CV2676460	single nucleotide variant	NM_014830.3(ZBTB39):c.494A>G (p.Tyr165Cys)	not specified [RCV004286475]	uncertain significance	12	57004424	57004424	Human		name
401729679	CV2690437	single nucleotide variant	NM_014830.3(ZBTB39):c.736C>T (p.Pro246Ser)	not specified [RCV004302420]	uncertain significance	12	57004182	57004182	Human		name
401771185	CV2700916	single nucleotide variant	NM_014830.3(ZBTB39):c.704C>T (p.Thr235Met)	not specified [RCV004307181]	likely benign	12	57004214	57004214	Human		name
401761557	CV2702387	single nucleotide variant	NM_014830.3(ZBTB39):c.362C>G (p.Thr121Ser)	not specified [RCV004316911]	uncertain significance	12	57004556	57004556	Human		name
401759716	CV2705690	single nucleotide variant	NM_014830.3(ZBTB39):c.404C>A (p.Thr135Asn)	not specified [RCV004318543]	uncertain significance	12	57004514	57004514	Human		name
401759719	CV2705691	single nucleotide variant	NM_014830.3(ZBTB39):c.714G>C (p.Gln238His)	not specified [RCV004318544]	uncertain significance	12	57004204	57004204	Human		name
401769601	CV2731453	single nucleotide variant	NM_014830.3(ZBTB39):c.605C>T (p.Pro202Leu)	not specified [RCV004330810]	uncertain significance	12	57004313	57004313	Human		name
401876932	CV2764221	single nucleotide variant	NM_014830.3(ZBTB39):c.929C>T (p.Ala310Val)	not specified [RCV004336762]	uncertain significance	12	57003989	57003989	Human		name
401862620	CV2775243	single nucleotide variant	NM_014830.3(ZBTB39):c.599C>T (p.Pro200Leu)	not specified [RCV004348370]	likely benign	12	57004319	57004319	Human		name
401894474	CV2788173	single nucleotide variant	NM_014830.3(ZBTB39):c.971A>G (p.Asp324Gly)	not specified [RCV004352791]	uncertain significance	12	57003947	57003947	Human		name
405808046	CV3356915	single nucleotide variant	NM_014830.3(ZBTB39):c.884A>T (p.Gln295Leu)	not specified [RCV004480985]	uncertain significance	12	57004034	57004034	Human		name
405808048	CV3356916	single nucleotide variant	NM_014830.3(ZBTB39):c.909C>G (p.Asp303Glu)	not specified [RCV004480986]	uncertain significance	12	57004009	57004009	Human		name
407466010	CV3494062	single nucleotide variant	NM_014830.3(ZBTB39):c.667A>G (p.Ser223Gly)	not specified [RCV004688920]	uncertain significance	12	57004251	57004251	Human		name
407466025	CV3494066	single nucleotide variant	NM_014830.3(ZBTB39):c.695C>T (p.Thr232Ile)	not specified [RCV004688924]	uncertain significance	12	57004223	57004223	Human		name
597693117	CV3624323	single nucleotide variant	NM_014830.3(ZBTB39):c.649C>T (p.Pro217Ser)	not specified [RCV004884848]	uncertain significance	12	57004269	57004269	Human		name
597693150	CV3624328	single nucleotide variant	NM_014830.3(ZBTB39):c.700A>G (p.Ser234Gly)	not specified [RCV004884852]	uncertain significance	12	57004218	57004218	Human		name
597693170	CV3624330	single nucleotide variant	NM_014830.3(ZBTB39):c.599C>A (p.Pro200Gln)	not specified [RCV004884854]	uncertain significance	12	57004319	57004319	Human		name
598243333	CV3930394	single nucleotide variant	NM_014830.3(ZBTB39):c.421C>T (p.His141Tyr)	not specified [RCV005297273]	uncertain significance	12	57004497	57004497	Human		name
598243346	CV3930399	single nucleotide variant	NM_014830.3(ZBTB39):c.925C>T (p.Pro309Ser)	not specified [RCV005297276]	uncertain significance	12	57003993	57003993	Human		name
156173127	CV2194321	single nucleotide variant	NM_014830.3(ZBTB39):c.1967C>T (p.Ser656Leu)	not specified [RCV004079436]	uncertain significance	12	57002951	57002951	Human		name
156243059	CV2262221	single nucleotide variant	NM_014830.3(ZBTB39):c.1227C>G (p.Phe409Leu)	not specified [RCV004128437]	uncertain significance	12	57003691	57003691	Human		name
155974131	CV2269919	single nucleotide variant	NM_014830.3(ZBTB39):c.1852A>G (p.Ser618Gly)	not specified [RCV004127133]	uncertain significance	12	57003066	57003066	Human		name
155986130	CV2282502	single nucleotide variant	NM_014830.3(ZBTB39):c.2129C>T (p.Pro710Leu)	not specified [RCV004135083]	uncertain significance	12	57002789	57002789	Human		name
156067953	CV2320343	single nucleotide variant	NM_014830.3(ZBTB39):c.1923C>A (p.Phe641Leu)	not specified [RCV004178505]	uncertain significance	12	57002995	57002995	Human		name
156077748	CV2331904	single nucleotide variant	NM_014830.3(ZBTB39):c.1015G>A (p.Glu339Lys)	not specified [RCV004186558]	uncertain significance	12	57003903	57003903	Human		name
155984984	CV2368031	single nucleotide variant	NM_014830.3(ZBTB39):c.1790A>G (p.Gln597Arg)	not specified [RCV004223115]	uncertain significance	12	57003128	57003128	Human		name
156392260	CV2378463	single nucleotide variant	NM_014830.3(ZBTB39):c.1090C>G (p.Arg364Gly)	not specified [RCV004228521]	uncertain significance	12	57003828	57003828	Human		name
156260898	CV2381247	single nucleotide variant	NM_014830.3(ZBTB39):c.1336G>A (p.Ala446Thr)	not specified [RCV004227312]	uncertain significance	12	57003582	57003582	Human		name
155955181	CV2389895	single nucleotide variant	NM_014830.3(ZBTB39):c.1012C>T (p.Arg338Trp)	not specified [RCV004236107]	uncertain significance	12	57003906	57003906	Human		name
156103891	CV2400245	single nucleotide variant	NM_014830.3(ZBTB39):c.1151G>A (p.Arg384Gln)	not specified [RCV004243037]	uncertain significance	12	57003767	57003767	Human		name
401721381	CV2673696	single nucleotide variant	NM_014830.3(ZBTB39):c.1664A>C (p.Tyr555Ser)	not specified [RCV004282425]	uncertain significance	12	57003254	57003254	Human		name
401738539	CV2711961	single nucleotide variant	NM_014830.3(ZBTB39):c.1535T>C (p.Val512Ala)	not specified [RCV004309572]	uncertain significance	12	57003383	57003383	Human		name
401767449	CV2729668	single nucleotide variant	NM_014830.3(ZBTB39):c.1462C>T (p.Arg488Cys)	not specified [RCV004331928]	uncertain significance	12	57003456	57003456	Human		name
405808034	CV3356909	single nucleotide variant	NM_014830.3(ZBTB39):c.1091G>A (p.Arg364Gln)	not specified [RCV004480979]	uncertain significance	12	57003827	57003827	Human		name
405808036	CV3356910	single nucleotide variant	NM_014830.3(ZBTB39):c.1258C>T (p.Arg420Trp)	not specified [RCV004480980]	uncertain significance	12	57003660	57003660	Human		name
405808038	CV3356911	single nucleotide variant	NM_014830.3(ZBTB39):c.1412T>C (p.Ile471Thr)	not specified [RCV004480981]	uncertain significance	12	57003506	57003506	Human		name
405808040	CV3356912	single nucleotide variant	NM_014830.3(ZBTB39):c.1915C>T (p.His639Tyr)	not specified [RCV004480982]	uncertain significance	12	57003003	57003003	Human		name
405808042	CV3356913	single nucleotide variant	NM_014830.3(ZBTB39):c.2066C>G (p.Pro689Arg)	not specified [RCV004480983]	uncertain significance	12	57002852	57002852	Human		name
407466014	CV3494063	single nucleotide variant	NM_014830.3(ZBTB39):c.1212G>A (p.Met404Ile)	not specified [RCV004688921]	uncertain significance	12	57003706	57003706	Human		name
407466017	CV3494064	single nucleotide variant	NM_014830.3(ZBTB39):c.1259G>A (p.Arg420Gln)	not specified [RCV004688922]	uncertain significance	12	57003659	57003659	Human		name
407466021	CV3494065	single nucleotide variant	NM_014830.3(ZBTB39):c.1256G>A (p.Arg419Gln)	not specified [RCV004688923]	uncertain significance	12	57003662	57003662	Human		name
407466029	CV3494067	single nucleotide variant	NM_014830.3(ZBTB39):c.1031C>T (p.Pro344Leu)	not specified [RCV004688925]	uncertain significance	12	57003887	57003887	Human		name
408367618	CV3511295	single nucleotide variant	NM_014830.3(ZBTB39):c.2092A>C (p.Met698Leu)	ZBTB39-related condition [RCV004759071]	uncertain significance	12	57002826	57002826	Human		name , trait
597752681	CV3624322	single nucleotide variant	NM_014830.3(ZBTB39):c.1717G>A (p.Gly573Arg)	not specified [RCV004893021]	uncertain significance	12	57003201	57003201	Human		name
597752685	CV3624324	single nucleotide variant	NM_014830.3(ZBTB39):c.1843G>T (p.Ala615Ser)	not specified [RCV004893022]	uncertain significance	12	57003075	57003075	Human		name
597693126	CV3624325	single nucleotide variant	NM_014830.3(ZBTB39):c.1567C>G (p.Leu523Val)	not specified [RCV004884849]	uncertain significance	12	57003351	57003351	Human		name
597693133	CV3624326	single nucleotide variant	NM_014830.3(ZBTB39):c.1360G>A (p.Ala454Thr)	not specified [RCV004884850]	uncertain significance	12	57003558	57003558	Human		name
597693142	CV3624327	single nucleotide variant	NM_014830.3(ZBTB39):c.1183A>G (p.Ile395Val)	not specified [RCV004884851]	uncertain significance	12	57003735	57003735	Human		name
597693162	CV3624329	single nucleotide variant	NM_014830.3(ZBTB39):c.1886G>C (p.Gly629Ala)	not specified [RCV004884853]	uncertain significance	12	57003032	57003032	Human		name
598196690	CV3930395	single nucleotide variant	NM_014830.3(ZBTB39):c.1259G>T (p.Arg420Leu)	not specified [RCV005313555]	uncertain significance	12	57003659	57003659	Human		name
598243337	CV3930396	single nucleotide variant	NM_014830.3(ZBTB39):c.1979T>A (p.Met660Lys)	not specified [RCV005297274]	uncertain significance	12	57002939	57002939	Human		name
598196697	CV3930397	single nucleotide variant	NM_014830.3(ZBTB39):c.1692T>G (p.Ser564Arg)	not specified [RCV005313556]	uncertain significance	12	57003226	57003226	Human		name
598243342	CV3930398	single nucleotide variant	NM_014830.3(ZBTB39):c.1682A>G (p.Lys561Arg)	not specified [RCV005297275]	uncertain significance	12	57003236	57003236	Human		name

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