Zdhhc13 Variant Search Result - Rat Genome Database

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47 records found for search term Zdhhc13

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156074524	CV2376977	single nucleotide variant	NM_019028.3(ZDHHC13):c.8G>C (p.Gly3Ala)	not specified [RCV004229659]	uncertain significance	11	19117257	19117257	Human		name
156254040	CV2193193	single nucleotide variant	NM_019028.3(ZDHHC13):c.71G>A (p.Arg24Gln)	not specified [RCV004071183]	uncertain significance	11	19143021	19143021	Human		name
329382967	CV2445718	single nucleotide variant	NM_019028.3(ZDHHC13):c.62G>C (p.Gly21Ala)	not specified [RCV004259788]	uncertain significance	11	19143012	19143012	Human		name
405812918	CV3349728	single nucleotide variant	NM_019028.3(ZDHHC13):c.67G>A (p.Gly23Ser)	not specified [RCV004483581]	uncertain significance	11	19143017	19143017	Human		name
407457235	CV3492065	single nucleotide variant	NM_019028.3(ZDHHC13):c.77G>A (p.Gly26Asp)	not specified [RCV004686250]	uncertain significance	11	19143027	19143027	Human		name
407457237	CV3492066	single nucleotide variant	NM_019028.3(ZDHHC13):c.375A>G (p.Arg125=)	not specified [RCV004686251]	likely benign	11	19149187	19149187	Human		name
597724554	CV3631003	single nucleotide variant	NM_019028.3(ZDHHC13):c.41G>A (p.Ser14Asn)	not specified [RCV004888180]	uncertain significance	11	19142991	19142991	Human		name
597793234	CV3630998	single nucleotide variant	NM_019028.3(ZDHHC13):c.152G>A (p.Cys51Tyr)	not specified [RCV004877249]	uncertain significance	11	19143102	19143102	Human		name
597793243	CV3631004	single nucleotide variant	NM_019028.3(ZDHHC13):c.135A>G (p.Ile45Met)	not specified [RCV004877252]	uncertain significance	11	19143085	19143085	Human		name
598258437	CV3926965	single nucleotide variant	NM_019028.3(ZDHHC13):c.157A>G (p.Ile53Val)	not specified [RCV005300020]	uncertain significance	11	19143107	19143107	Human		name
156136984	CV2210339	single nucleotide variant	NM_019028.3(ZDHHC13):c.490A>G (p.Ile164Val)	not specified [RCV004089494]	uncertain significance	11	19149302	19149302	Human		name
155904872	CV2298884	single nucleotide variant	NM_019028.3(ZDHHC13):c.574A>G (p.Lys192Glu)	not specified [RCV004156424]	uncertain significance	11	19150781	19150781	Human		name
156150563	CV2307487	single nucleotide variant	NM_019028.3(ZDHHC13):c.495A>G (p.Ile165Met)	not specified [RCV004166143]	uncertain significance	11	19149307	19149307	Human		name
156196245	CV2319082	single nucleotide variant	NM_019028.3(ZDHHC13):c.781A>C (p.Lys261Gln)	not specified [RCV004178162]	uncertain significance	11	19152592	19152592	Human		name
156166772	CV2373630	single nucleotide variant	NM_019028.3(ZDHHC13):c.893T>C (p.Leu298Pro)	not specified [RCV004222721]	uncertain significance	11	19155815	19155815	Human		name
156059625	CV2391781	single nucleotide variant	NM_019028.3(ZDHHC13):c.541A>G (p.Asn181Asp)	not specified [RCV004235663]	uncertain significance	11	19150748	19150748	Human		name
401783078	CV2703767	single nucleotide variant	NM_019028.3(ZDHHC13):c.804G>A (p.Met268Ile)	not specified [RCV004306641]	uncertain significance	11	19152615	19152615	Human		name
401741784	CV2710270	single nucleotide variant	NM_019028.3(ZDHHC13):c.413A>G (p.His138Arg)	not specified [RCV004317163]	uncertain significance	11	19149225	19149225	Human		name
401859359	CV2771547	single nucleotide variant	NM_019028.3(ZDHHC13):c.352A>T (p.Thr118Ser)	not specified [RCV004348574]	uncertain significance	11	19147651	19147651	Human		name
405812915	CV3349726	single nucleotide variant	NM_019028.3(ZDHHC13):c.503T>G (p.Leu168Arg)	not specified [RCV004483579]	uncertain significance	11	19149315	19149315	Human		name
405812916	CV3349727	single nucleotide variant	NM_019028.3(ZDHHC13):c.551C>T (p.Thr184Ile)	not specified [RCV004483580]	uncertain significance	11	19150758	19150758	Human		name
405812920	CV3349729	single nucleotide variant	NM_019028.3(ZDHHC13):c.789G>C (p.Gln263His)	not specified [RCV004483582]	uncertain significance	11	19152600	19152600	Human		name
405812921	CV3349730	single nucleotide variant	NM_019028.3(ZDHHC13):c.917T>C (p.Ile306Thr)	not specified [RCV004483583]	uncertain significance	11	19155839	19155839	Human		name
405812923	CV3349731	single nucleotide variant	NM_019028.3(ZDHHC13):c.971T>C (p.Leu324Pro)	not specified [RCV004483584]	uncertain significance	11	19155893	19155893	Human		name
407457233	CV3492064	single nucleotide variant	NM_019028.3(ZDHHC13):c.871G>A (p.Glu291Lys)	not specified [RCV004686249]	uncertain significance	11	19152682	19152682	Human		name
407457241	CV3492067	single nucleotide variant	NM_019028.3(ZDHHC13):c.934T>C (p.Phe312Leu)	not specified [RCV004686252]	uncertain significance	11	19155856	19155856	Human		name
597793246	CV3631005	single nucleotide variant	NM_019028.3(ZDHHC13):c.460C>T (p.His154Tyr)	not specified [RCV004877253]	uncertain significance	11	19149272	19149272	Human		name
597793247	CV3631006	single nucleotide variant	NM_019028.3(ZDHHC13):c.313G>C (p.Gly105Arg)	not specified [RCV004877254]	uncertain significance	11	19147612	19147612	Human		name
598258408	CV3926958	single nucleotide variant	NM_019028.3(ZDHHC13):c.380G>A (p.Gly127Glu)	not specified [RCV005300014]	uncertain significance	11	19149192	19149192	Human		name
598258427	CV3926963	single nucleotide variant	NM_019028.3(ZDHHC13):c.840G>T (p.Lys280Asn)	not specified [RCV005300018]	likely benign	11	19152651	19152651	Human		name
156128891	CV2220095	single nucleotide variant	NM_019028.3(ZDHHC13):c.1651A>T (p.Thr551Ser)	not specified [RCV004093968]	uncertain significance	11	19172741	19172741	Human		name
155973748	CV2332435	single nucleotide variant	NM_019028.3(ZDHHC13):c.1522A>G (p.Thr508Ala)	not specified [RCV004196166]	uncertain significance	11	19170458	19170458	Human		name
156208665	CV2370014	single nucleotide variant	NM_019028.3(ZDHHC13):c.1135A>G (p.Ser379Gly)	not specified [RCV004210912]	uncertain significance	11	19163329	19163329	Human		name
329392409	CV2468061	single nucleotide variant	NM_019028.3(ZDHHC13):c.1645G>C (p.Gly549Arg)	not specified [RCV004275672]	uncertain significance	11	19172735	19172735	Human		name
401756237	CV2687046	single nucleotide variant	NM_019028.3(ZDHHC13):c.1859G>C (p.Arg620Pro)	not specified [RCV004304368]	uncertain significance	11	19175950	19175950	Human		name
401773037	CV2709090	single nucleotide variant	NM_019028.3(ZDHHC13):c.1784T>C (p.Leu595Ser)	not specified [RCV004314425]	uncertain significance	11	19175875	19175875	Human		name
405813473	CV3349725	single nucleotide variant	NM_019028.3(ZDHHC13):c.1343G>A (p.Cys448Tyr)	not specified [RCV004483578]	uncertain significance	11	19165098	19165098	Human		name
597724532	CV3630999	single nucleotide variant	NM_019028.3(ZDHHC13):c.1724C>T (p.Pro575Leu)	not specified [RCV004888178]	uncertain significance	11	19172814	19172814	Human		name
597793235	CV3631000	single nucleotide variant	NM_019028.3(ZDHHC13):c.1718A>G (p.Lys573Arg)	not specified [RCV004877250]	likely benign	11	19172808	19172808	Human		name
597724543	CV3631001	single nucleotide variant	NM_019028.3(ZDHHC13):c.1673T>A (p.Leu558Gln)	not specified [RCV004888179]	uncertain significance	11	19172763	19172763	Human		name
597793239	CV3631002	single nucleotide variant	NM_019028.3(ZDHHC13):c.1623A>T (p.Gln541His)	not specified [RCV004877251]	uncertain significance	11	19170559	19170559	Human		name
598258403	CV3926957	single nucleotide variant	NM_019028.3(ZDHHC13):c.1859G>A (p.Arg620His)	not specified [RCV005300013]	uncertain significance	11	19175950	19175950	Human		name
598258414	CV3926960	single nucleotide variant	NM_019028.3(ZDHHC13):c.1441G>A (p.Val481Ile)	not specified [RCV005300015]	uncertain significance	11	19166352	19166352	Human		name
598258418	CV3926961	single nucleotide variant	NM_019028.3(ZDHHC13):c.1089G>C (p.Trp363Cys)	not specified [RCV005300016]	uncertain significance	11	19159021	19159021	Human		name
598258422	CV3926962	single nucleotide variant	NM_019028.3(ZDHHC13):c.1639T>C (p.Phe547Leu)	not specified [RCV005300017]	uncertain significance	11	19172729	19172729	Human		name
598258432	CV3926964	single nucleotide variant	NM_019028.3(ZDHHC13):c.1295T>C (p.Leu432Pro)	not specified [RCV005300019]	uncertain significance	11	19164362	19164362	Human		name
15193319	CV724353	single nucleotide variant	NM_019028.3(ZDHHC13):c.1210G>A (p.Ala404Thr)	not provided [RCV000888913]	likely benign	11	19163404	19163404	Human		name

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