Cc2d2b Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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39 records found for search term Cc2d2b

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401907645	CV2809507	single nucleotide variant	NM_001349008.3(CC2D2B):c.265T>C (p.Leu89=)	not provided [RCV003422768]	likely benign	10	95927261	95927261	Human		name
401907646	CV2809508	single nucleotide variant	NM_001349008.3(CC2D2B):c.1140G>A (p.Arg380=)	not provided [RCV003422769]	likely benign	10	95961859	95961859	Human		name
401904525	CV2809509	single nucleotide variant	NM_001349008.3(CC2D2B):c.1992C>T (p.Leu664=)	not provided [RCV003422770]	likely benign	10	95982023	95982023	Human		name
156402650	CV2371347	single nucleotide variant	NM_001349008.3(CC2D2B):c.411G>C (p.Glu137Asp)	not specified [RCV004223353]	likely benign	10	95938065	95938065	Human		name
405754023	CV3292221	single nucleotide variant	NM_001349008.3(CC2D2B):c.2972G>T (p.Gly991Val)	not specified [RCV004432550]	uncertain significance	10	96009850	96009850	Human		name
155973120	CV2224546	single nucleotide variant	NM_001349008.3(CC2D2B):c.3617C>T (p.Thr1206Met)	not specified [RCV004098126]	uncertain significance	10	96016301	96016301	Human		name
156266150	CV2275454	single nucleotide variant	NM_001349008.3(CC2D2B):c.3433A>T (p.Ile1145Phe)	not specified [RCV004135325]	uncertain significance	10	96013794	96013794	Human		name
156142036	CV2288637	single nucleotide variant	NM_001349008.3(CC2D2B):c.3040T>C (p.Ser1014Pro)	not specified [RCV004152148]	uncertain significance	10	96009918	96009918	Human		name
156290521	CV2324913	single nucleotide variant	NM_001349008.3(CC2D2B):c.3491G>C (p.Gly1164Ala)	not specified [RCV004175174]	uncertain significance	10	96013852	96013852	Human		name
401766847	CV2680170	single nucleotide variant	NM_001349008.3(CC2D2B):c.4286A>G (p.Tyr1429Cys)	not specified [RCV004286651]	uncertain significance	10	96031980	96031980	Human		name
401730027	CV2683911	single nucleotide variant	NM_001349008.3(CC2D2B):c.4265A>G (p.Asn1422Ser)	not specified [RCV004284631]	uncertain significance	10	96031959	96031959	Human		name
401727124	CV2684479	single nucleotide variant	NM_001349008.3(CC2D2B):c.3302G>A (p.Arg1101Gln)	not specified [RCV004291552]	uncertain significance	10	96012605	96012605	Human		name
401757247	CV2692887	single nucleotide variant	NM_001349008.3(CC2D2B):c.3602T>C (p.Leu1201Pro)	not specified [RCV004306418]	uncertain significance	10	96016286	96016286	Human		name
401782943	CV2707623	single nucleotide variant	NM_001349008.3(CC2D2B):c.3686C>G (p.Pro1229Arg)	not specified [RCV004306563]	uncertain significance	10	96019258	96019258	Human		name
401876980	CV2767784	single nucleotide variant	NM_001349008.3(CC2D2B):c.3779T>G (p.Ile1260Ser)	not specified [RCV004345909]	uncertain significance	10	96019715	96019715	Human		name
401890935	CV2768834	single nucleotide variant	NM_001349008.3(CC2D2B):c.3646G>A (p.Val1216Ile)	not specified [RCV004346955]	uncertain significance	10	96019218	96019218	Human		name
401894559	CV2788427	single nucleotide variant	NM_001349008.3(CC2D2B):c.3925A>T (p.Met1309Leu)	not specified [RCV004354955]	uncertain significance	10	96024889	96024889	Human		name
405754007	CV3292219	single nucleotide variant	NM_001349008.3(CC2D2B):c.3523A>G (p.Ile1175Val)	not specified [RCV004432548]	uncertain significance	10	96016207	96016207	Human		name
405754017	CV3292220	single nucleotide variant	NM_001349008.3(CC2D2B):c.3536T>C (p.Ile1179Thr)	not specified [RCV004432549]	uncertain significance	10	96016220	96016220	Human		name
405754033	CV3292222	single nucleotide variant	NM_001349008.3(CC2D2B):c.3647T>C (p.Val1216Ala)	not specified [RCV004432551]	uncertain significance	10	96019219	96019219	Human		name
405754041	CV3292223	single nucleotide variant	NM_001349008.3(CC2D2B):c.3697C>A (p.Gln1233Lys)	not specified [RCV004432552]	uncertain significance	10	96019269	96019269	Human		name
405754048	CV3292224	single nucleotide variant	NM_001349008.3(CC2D2B):c.3902T>C (p.Ile1301Thr)	not specified [RCV004432553]	uncertain significance	10	96024866	96024866	Human		name
407482888	CV3422058	single nucleotide variant	NM_001349008.3(CC2D2B):c.4016A>G (p.Gln1339Arg)	not specified [RCV004602747]	uncertain significance	10	96027280	96027280	Human		name
407482895	CV3422059	single nucleotide variant	NM_001349008.3(CC2D2B):c.4034G>C (p.Arg1345Pro)	not specified [RCV004602748]	uncertain significance	10	96027298	96027298	Human		name
407454418	CV3422060	single nucleotide variant	NM_001349008.3(CC2D2B):c.3986G>A (p.Arg1329Gln)	not specified [RCV004609801]	uncertain significance	10	96027250	96027250	Human		name
407482900	CV3422061	single nucleotide variant	NM_001349008.3(CC2D2B):c.4130C>T (p.Thr1377Met)	not specified [RCV004602749]	uncertain significance	10	96031824	96031824	Human		name
407482907	CV3422062	single nucleotide variant	NM_001349008.3(CC2D2B):c.3473C>A (p.Thr1158Lys)	not specified [RCV004602750]	uncertain significance	10	96013834	96013834	Human		name
407482914	CV3422063	single nucleotide variant	NM_001349008.3(CC2D2B):c.4073T>G (p.Phe1358Cys)	not specified [RCV004602751]	uncertain significance	10	96027337	96027337	Human		name
407482918	CV3422064	single nucleotide variant	NM_001349008.3(CC2D2B):c.3904T>G (p.Tyr1302Asp)	not specified [RCV004602752]	uncertain significance	10	96024868	96024868	Human		name
407482924	CV3422065	single nucleotide variant	NM_001349008.3(CC2D2B):c.3811T>C (p.Phe1271Leu)	not specified [RCV004602753]	uncertain significance	10	96019747	96019747	Human		name
407482931	CV3422066	single nucleotide variant	NM_001349008.3(CC2D2B):c.3796C>A (p.Pro1266Thr)	not specified [RCV004602754]	uncertain significance	10	96019732	96019732	Human		name
597785992	CV3637893	single nucleotide variant	NM_001349008.3(CC2D2B):c.3361A>G (p.Ile1121Val)	not specified [RCV004900869]	uncertain significance	10	96012664	96012664	Human		name
597785996	CV3637894	single nucleotide variant	NM_001349008.3(CC2D2B):c.3936T>G (p.Asp1312Glu)	not specified [RCV004900870]	uncertain significance	10	96024900	96024900	Human		name
597785999	CV3637895	single nucleotide variant	NM_001349008.3(CC2D2B):c.3846G>C (p.Leu1282Phe)	not specified [RCV004900871]	uncertain significance	10	96019782	96019782	Human		name
597786004	CV3637896	single nucleotide variant	NM_001349008.3(CC2D2B):c.3739G>A (p.Val1247Ile)	not specified [RCV004900872]	uncertain significance	10	96019311	96019311	Human		name
597760611	CV3637897	single nucleotide variant	NM_001349008.3(CC2D2B):c.3713T>C (p.Phe1238Ser)	not specified [RCV004894808]	uncertain significance	10	96019285	96019285	Human		name
598176596	CV3950520	single nucleotide variant	NM_001349008.3(CC2D2B):c.3736A>T (p.Ser1246Cys)	not specified [RCV005310060]	uncertain significance	10	96019308	96019308	Human		name
598176601	CV3950521	single nucleotide variant	NM_001349008.3(CC2D2B):c.4215T>A (p.Phe1405Leu)	not specified [RCV005310061]	uncertain significance	10	96031909	96031909	Human		name
598176608	CV3950522	single nucleotide variant	NM_001349008.3(CC2D2B):c.3719C>T (p.Pro1240Leu)	not specified [RCV005310062]	uncertain significance	10	96019291	96019291	Human		name

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