Znf689 Variant Search Result - Rat Genome Database

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33 records found for search term Znf689

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156065552	CV2287379	single nucleotide variant	NM_138447.3(ZNF689):c.25C>T (p.Pro9Ser)	not specified [RCV004146989]	likely benign	16	30610017	30610017	Human		name
156050959	CV2269323	single nucleotide variant	NM_138447.3(ZNF689):c.55A>G (p.Ser19Gly)	not specified [RCV004130727]	likely benign	16	30609987	30609987	Human		name
401864566	CV2777894	single nucleotide variant	NM_138447.3(ZNF689):c.99C>A (p.Asp33Glu)	not specified [RCV004347863]	uncertain significance	16	30609943	30609943	Human		name
597733797	CV3642211	single nucleotide variant	NM_138447.3(ZNF689):c.58C>T (p.Arg20Trp)	not specified [RCV004889216]	uncertain significance	16	30609984	30609984	Human		name
155926044	CV2348596	single nucleotide variant	NM_138447.3(ZNF689):c.283C>T (p.Pro95Ser)	not specified [RCV004195824]	uncertain significance	16	30609561	30609561	Human		name
401735602	CV2702820	single nucleotide variant	NM_138447.3(ZNF689):c.110A>T (p.Tyr37Phe)	not specified [RCV004319379]	uncertain significance	16	30609932	30609932	Human		name
401867499	CV2770471	single nucleotide variant	NM_138447.3(ZNF689):c.269C>T (p.Pro90Leu)	not specified [RCV004358108]	uncertain significance	16	30609575	30609575	Human		name
597733829	CV3642216	single nucleotide variant	NM_138447.3(ZNF689):c.178G>A (p.Glu60Lys)	not specified [RCV004889221]	uncertain significance	16	30609864	30609864	Human		name
155992524	CV2253474	single nucleotide variant	NM_138447.3(ZNF689):c.356T>G (p.Val119Gly)	not specified [RCV004125191]	uncertain significance	16	30605411	30605411	Human		name
156069926	CV2292859	single nucleotide variant	NM_138447.3(ZNF689):c.967G>C (p.Glu323Gln)	not specified [RCV004148368]	uncertain significance	16	30604800	30604800	Human		name
156332416	CV2339778	single nucleotide variant	NM_138447.3(ZNF689):c.463G>A (p.Gly155Ser)	not specified [RCV004196475]	uncertain significance	16	30605304	30605304	Human		name
329374685	CV2431009	single nucleotide variant	NM_138447.3(ZNF689):c.539C>T (p.Pro180Leu)	not specified [RCV004250383]	uncertain significance	16	30605228	30605228	Human		name
401897821	CV2772957	single nucleotide variant	NM_138447.3(ZNF689):c.424C>T (p.Pro142Ser)	not specified [RCV004357723]	uncertain significance	16	30605343	30605343	Human		name
401878923	CV2773802	single nucleotide variant	NM_138447.3(ZNF689):c.766A>G (p.Thr256Ala)	not specified [RCV004358254]	uncertain significance	16	30605001	30605001	Human		name
405687525	CV3354775	single nucleotide variant	NM_138447.3(ZNF689):c.373G>A (p.Ala125Thr)	not specified [RCV004490072]	uncertain significance	16	30605394	30605394	Human		name
405687529	CV3354776	single nucleotide variant	NM_138447.3(ZNF689):c.637C>T (p.Arg213Cys)	not specified [RCV004490073]	uncertain significance	16	30605130	30605130	Human		name
407478313	CV3427229	single nucleotide variant	NM_138447.3(ZNF689):c.501C>A (p.His167Gln)	not specified [RCV004601734]	uncertain significance	16	30605266	30605266	Human		name
597733790	CV3642210	single nucleotide variant	NM_138447.3(ZNF689):c.959C>T (p.Pro320Leu)	not specified [RCV004889215]	uncertain significance	16	30604808	30604808	Human		name
597733811	CV3642213	single nucleotide variant	NM_138447.3(ZNF689):c.326G>A (p.Arg109Lys)	not specified [RCV004889218]	uncertain significance	16	30605441	30605441	Human		name
597733816	CV3642214	single nucleotide variant	NM_138447.3(ZNF689):c.323G>A (p.Ser108Asn)	not specified [RCV004889219]	uncertain significance	16	30605444	30605444	Human		name
598262441	CV3948934	single nucleotide variant	NM_138447.3(ZNF689):c.754C>T (p.Arg252Trp)	not specified [RCV005300789]	uncertain significance	16	30605013	30605013	Human		name
156060035	CV2239401	single nucleotide variant	NM_138447.3(ZNF689):c.1355C>A (p.Thr452Lys)	not specified [RCV004114131]	uncertain significance	16	30604412	30604412	Human		name
156087660	CV2259000	single nucleotide variant	NM_138447.3(ZNF689):c.1323G>C (p.Trp441Cys)	not specified [RCV004120271]	uncertain significance	16	30604444	30604444	Human		name
155975954	CV2327998	single nucleotide variant	NM_138447.3(ZNF689):c.1139G>A (p.Arg380His)	not specified [RCV004179308]	uncertain significance	16	30604628	30604628	Human		name
156103710	CV2386919	single nucleotide variant	NM_138447.3(ZNF689):c.1259G>A (p.Arg420Gln)	not specified [RCV004233550]	uncertain significance	16	30604508	30604508	Human		name
401726866	CV2674579	single nucleotide variant	NM_138447.3(ZNF689):c.1468A>G (p.Ile490Val)	not specified [RCV004291453]	uncertain significance	16	30604299	30604299	Human		name
401741999	CV2676871	single nucleotide variant	NM_138447.3(ZNF689):c.1237C>G (p.Pro413Ala)	not specified [RCV004291036]	uncertain significance	16	30604530	30604530	Human		name
401873201	CV2779754	single nucleotide variant	NM_138447.3(ZNF689):c.1106G>T (p.Gly369Val)	not specified [RCV004353392]	uncertain significance	16	30604661	30604661	Human		name
405687519	CV3354774	single nucleotide variant	NM_138447.3(ZNF689):c.1264G>A (p.Val422Met)	not specified [RCV004490071]	uncertain significance	16	30604503	30604503	Human		name
407478306	CV3427228	single nucleotide variant	NM_138447.3(ZNF689):c.1447A>G (p.Asn483Asp)	not specified [RCV004601733]	uncertain significance	16	30604320	30604320	Human		name
407478320	CV3427230	single nucleotide variant	NM_138447.3(ZNF689):c.1031C>G (p.Pro344Arg)	not specified [RCV004601735]	uncertain significance	16	30604736	30604736	Human		name
597733805	CV3642212	single nucleotide variant	NM_138447.3(ZNF689):c.1250C>T (p.Ala417Val)	not specified [RCV004889217]	uncertain significance	16	30604517	30604517	Human		name
597733822	CV3642215	single nucleotide variant	NM_138447.3(ZNF689):c.1451G>A (p.Cys484Tyr)	not specified [RCV004889220]	uncertain significance	16	30604316	30604316	Human		name

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