Zbtb33 Variant Search Result - Rat Genome Database

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42 records found for search term Zbtb33

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401929113	CV2826911	single nucleotide variant	NM_001184742.2(ZBTB33):c.*1127T>G	not provided [RCV003439723]	benign	X	120256561	120256561	Human		name
401929104	CV2826908	single nucleotide variant	NM_001184742.2(ZBTB33):c.-105+814G>A	not provided [RCV003439720]	likely benign	X	120251791	120251791	Human		name
401929108	CV2826909	single nucleotide variant	NM_001184742.2(ZBTB33):c.105C>T (p.Thr35=)	not provided [RCV003439721]	likely benign	X	120253520	120253520	Human		name
12740897	CV360516	single nucleotide variant	NM_001184742.2(ZBTB33):c.37C>G (p.Gln13Glu)	not specified [RCV000413439]	uncertain significance	X	120253452	120253452	Human		name
597693349	CV3627755	single nucleotide variant	NM_001184742.2(ZBTB33):c.53T>G (p.Leu18Arg)	not specified [RCV004884828]	uncertain significance	X	120253468	120253468	Human		name
597692967	CV3627761	single nucleotide variant	NM_001184742.2(ZBTB33):c.34A>C (p.Ile12Leu)	not specified [RCV004884832]	uncertain significance	X	120253449	120253449	Human		name
8637733	CV92959	single nucleotide variant	NM_006777.3(ZBTB33):c.1283C>T (p.Ser428Leu)	Malignant melanoma [RCV000073057]	not provided	X	120254698	120254698	Human		name
401929111	CV2826910	single nucleotide variant	NM_001184742.2(ZBTB33):c.1326T>C (p.Tyr442=)	not provided [RCV003439722]	likely benign	X	120254741	120254741	Human		name
405807901	CV3356868	single nucleotide variant	NM_001184742.2(ZBTB33):c.163A>G (p.Thr55Ala)	not specified [RCV004480938]	uncertain significance	X	120253578	120253578	Human		name
329356179	CV2442493	single nucleotide variant	NM_001184742.2(ZBTB33):c.856A>G (p.Thr286Ala)	not specified [RCV004266732]	likely benign	X	120254271	120254271	Human		name
401886616	CV2771344	single nucleotide variant	NM_001184742.2(ZBTB33):c.623T>C (p.Leu208Ser)	not specified [RCV004348105]	uncertain significance	X	120254038	120254038	Human		name
401862493	CV2775330	single nucleotide variant	NM_001184742.2(ZBTB33):c.592T>G (p.Cys198Gly)	not specified [RCV004348441]	uncertain significance	X	120254007	120254007	Human		name
405807911	CV3356873	single nucleotide variant	NM_001184742.2(ZBTB33):c.389C>T (p.Ala130Val)	not specified [RCV004480943]	uncertain significance	X	120253804	120253804	Human		name
405807913	CV3356874	single nucleotide variant	NM_001184742.2(ZBTB33):c.458A>G (p.Lys153Arg)	not specified [RCV004480944]	uncertain significance	X	120253873	120253873	Human		name
405807915	CV3356875	single nucleotide variant	NM_001184742.2(ZBTB33):c.787G>A (p.Gly263Arg)	not specified [RCV004480945]	uncertain significance	X	120254202	120254202	Human		name
407465961	CV3494050	single nucleotide variant	NM_001184742.2(ZBTB33):c.836A>G (p.Asn279Ser)	not specified [RCV004688908]	uncertain significance	X	120254251	120254251	Human		name
597693383	CV3627752	single nucleotide variant	NM_001184742.2(ZBTB33):c.766G>T (p.Ala256Ser)	not specified [RCV004884825]	uncertain significance	X	120254181	120254181	Human		name
597692989	CV3627759	single nucleotide variant	NM_001184742.2(ZBTB33):c.545A>G (p.Lys182Arg)	not specified [RCV004884830]	uncertain significance	X	120253960	120253960	Human		name
597692959	CV3627760	single nucleotide variant	NM_001184742.2(ZBTB33):c.626C>T (p.Pro209Leu)	not specified [RCV004884831]	uncertain significance	X	120254041	120254041	Human		name
13518665	CV486507	single nucleotide variant	NM_001184742.2(ZBTB33):c.653A>T (p.Gln218Leu)	not provided [RCV000584995]	uncertain significance	X	120254068	120254068	Human		name
15136903	CV717620	single nucleotide variant	NM_001184742.2(ZBTB33):c.676A>G (p.Ile226Val)	not provided [RCV000965526]	benign	X	120254091	120254091	Human		name
155990740	CV2280993	single nucleotide variant	NM_001184742.2(ZBTB33):c.1397C>A (p.Thr466Lys)	not specified [RCV004145494]	uncertain significance	X	120254812	120254812	Human		name
156018401	CV2302845	single nucleotide variant	NM_001184742.2(ZBTB33):c.1003A>C (p.Ile335Leu)	not specified [RCV004162745]	uncertain significance	X	120254418	120254418	Human		name
156171850	CV2337552	single nucleotide variant	NM_001184742.2(ZBTB33):c.1705A>G (p.Ile569Val)	not specified [RCV004187978]	uncertain significance	X	120255120	120255120	Human		name
156017243	CV2370075	single nucleotide variant	NM_001184742.2(ZBTB33):c.1912A>G (p.Met638Val)	not specified [RCV004210970]	uncertain significance	X	120255327	120255327	Human		name
156256574	CV2397786	single nucleotide variant	NM_001184742.2(ZBTB33):c.1408G>A (p.Glu470Lys)	not specified [RCV004239262]	uncertain significance	X	120254823	120254823	Human		name
401762392	CV2723423	single nucleotide variant	NM_001184742.2(ZBTB33):c.1048G>A (p.Val350Ile)	not specified [RCV004323498]	uncertain significance	X	120254463	120254463	Human		name
405807895	CV3356865	single nucleotide variant	NM_001184742.2(ZBTB33):c.1200T>G (p.Asn400Lys)	not specified [RCV004480935]	uncertain significance	X	120254615	120254615	Human		name
405807896	CV3356866	single nucleotide variant	NM_001184742.2(ZBTB33):c.1229T>C (p.Met410Thr)	not specified [RCV004480936]	uncertain significance	X	120254644	120254644	Human		name
405807903	CV3356869	single nucleotide variant	NM_001184742.2(ZBTB33):c.1707A>G (p.Ile569Met)	not specified [RCV004480939]	uncertain significance	X	120255122	120255122	Human		name
405807904	CV3356870	single nucleotide variant	NM_001184742.2(ZBTB33):c.1843A>G (p.Ile615Val)	not specified [RCV004480940]	uncertain significance	X	120255258	120255258	Human		name
405807907	CV3356871	single nucleotide variant	NM_001184742.2(ZBTB33):c.1882G>A (p.Gly628Arg)	not specified [RCV004480941]	uncertain significance	X	120255297	120255297	Human		name
405807909	CV3356872	single nucleotide variant	NM_001184742.2(ZBTB33):c.1979G>A (p.Gly660Asp)	not specified [RCV004480942]	uncertain significance	X	120255394	120255394	Human		name
407465965	CV3494051	single nucleotide variant	NM_001184742.2(ZBTB33):c.1189A>G (p.Arg397Gly)	not specified [RCV004688909]	uncertain significance	X	120254604	120254604	Human		name
597693372	CV3627753	single nucleotide variant	NM_001184742.2(ZBTB33):c.1153C>A (p.Leu385Ile)	not specified [RCV004884826]	uncertain significance	X	120254568	120254568	Human		name
597693360	CV3627754	single nucleotide variant	NM_001184742.2(ZBTB33):c.1426A>G (p.Met476Val)	not specified [RCV004884827]	uncertain significance	X	120254841	120254841	Human		name
597752662	CV3627756	single nucleotide variant	NM_001184742.2(ZBTB33):c.1364G>A (p.Gly455Glu)	not specified [RCV004893017]	uncertain significance	X	120254779	120254779	Human		name
597693339	CV3627758	single nucleotide variant	NM_001184742.2(ZBTB33):c.1024A>G (p.Ile342Val)	not specified [RCV004884829]	uncertain significance	X	120254439	120254439	Human		name
598243274	CV3930374	single nucleotide variant	NM_001184742.2(ZBTB33):c.1478A>G (p.Tyr493Cys)	not specified [RCV005297262]	uncertain significance	X	120254893	120254893	Human		name
598196626	CV3930375	single nucleotide variant	NM_001184742.2(ZBTB33):c.1277G>A (p.Gly426Asp)	not specified [RCV005313546]	uncertain significance	X	120254692	120254692	Human		name
15121480	CV717621	single nucleotide variant	NM_001184742.2(ZBTB33):c.1873C>A (p.Pro625Thr)	not provided [RCV000962902]	benign	X	120255288	120255288	Human		name
150443056	CV1266335	insertion	NM_001184742.2(ZBTB33):c.564_565insTGA (p.Asp189Ter)	not provided [RCV001690771]	benign	X	120253979	120253980	Human		name

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