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Variants search result for Homo sapiens
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51 records found for search term Ccni
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156329433CV2213837single nucleotide variantNM_006835.3(CCNI):c.179A>G (p.Asn60Ser)not specified [RCV004089892]uncertain significance47705857177058571Humanname
405741421CV3292672single nucleotide variantNM_006835.3(CCNI):c.238G>A (p.Val80Ile)not specified [RCV004430761]uncertain significance47705851277058512Humanname
597766063CV3641702single nucleotide variantNM_006835.3(CCNI):c.202C>G (p.Leu68Val)not specified [RCV004896058]uncertain significance47705854877058548Humanname
156312104CV2256817single nucleotide variantNM_006835.3(CCNI):c.733C>T (p.His245Tyr)not specified [RCV004121037]uncertain significance47704862077048620Humanname
401718812CV2679316single nucleotide variantNM_006835.3(CCNI):c.899T>C (p.Val300Ala)not specified [RCV004285856]uncertain significance47704845477048454Humanname
401737897CV2703689single nucleotide variantNM_006835.3(CCNI):c.568G>A (p.Ala190Thr)not specified [RCV004315940]uncertain significance47705527277055272Humanname
405741426CV3292673single nucleotide variantNM_006835.3(CCNI):c.616A>G (p.Met206Val)not specified [RCV004430762]uncertain significance47705522477055224Humanname
597762167CV3641704single nucleotide variantNM_006835.3(CCNI):c.397A>C (p.Ile133Leu)not specified [RCV004895095]uncertain significance47705602477056024Humanname
597766067CV3641705single nucleotide variantNM_006835.3(CCNI):c.950A>G (p.Lys317Arg)not specified [RCV004896059]uncertain significance47704840377048403Humanname
598228365CV3939806single nucleotide variantNM_006835.3(CCNI):c.601A>C (p.Met201Leu)not specified [RCV005319073]uncertain significance47705523977055239Humanname
597766062CV3641701single nucleotide variantNM_006835.3(CCNI):c.1055C>G (p.Ser352Cys)not specified [RCV004896057]uncertain significance47704829877048298Humanname
597762163CV3641703single nucleotide variantNM_006835.3(CCNI):c.1082A>G (p.Gln361Arg)not specified [RCV004895094]uncertain significance47704827177048271Humanname
597762172CV3641706single nucleotide variantNM_006835.3(CCNI):c.1009A>T (p.Ile337Phe)not specified [RCV004895096]uncertain significance47704834477048344Humanname
598205260CV3939808single nucleotide variantNM_001039780.4(CCNI2):c.5C>T (p.Ala2Val)not specified [RCV005314926]uncertain significance5132747500132747500Humanname
156238094CV2207060single nucleotide variantNM_001039780.4(CCNI2):c.92A>G (p.Glu31Gly)not specified [RCV004085670]uncertain significance5132747587132747587Humanname
401915036CV2827993single nucleotide variantNM_001039780.4(CCNI2):c.753G>A (p.Thr251=)not provided [RCV003428603]likely benign5132750976132750976Humanname
405741469CV3292679single nucleotide variantNM_001039780.4(CCNI2):c.30G>C (p.Gln10His)not specified [RCV004430768]uncertain significance5132747525132747525Humanname
405741490CV3292682single nucleotide variantNM_001039780.4(CCNI2):c.88C>A (p.Leu30Met)not specified [RCV004430771]uncertain significance5132747583132747583Humanname
156158754CV2236128single nucleotide variantNM_001039780.4(CCNI2):c.139C>T (p.Pro47Ser)not specified [RCV004114274]likely benign5132747634132747634Humanname
155988692CV2371849single nucleotide variantNM_001039780.4(CCNI2):c.235C>G (p.Arg79Gly)not specified [RCV004221543]uncertain significance5132747730132747730Humanname
329385256CV2432067single nucleotide variantNM_001039780.4(CCNI2):c.131G>A (p.Gly44Glu)not specified [RCV004249218]uncertain significance5132747626132747626Humanname
405741441CV3292675single nucleotide variantNM_001039780.4(CCNI2):c.220G>T (p.Val74Phe)not specified [RCV004430764]uncertain significance5132747715132747715Humanname
405741446CV3292676single nucleotide variantNM_001039780.4(CCNI2):c.270C>A (p.Asp90Glu)not specified [RCV004430765]uncertain significance5132747765132747765Humanname
597766071CV3641707single nucleotide variantNM_001039780.4(CCNI2):c.245C>T (p.Thr82Met)not specified [RCV004896060]uncertain significance5132747740132747740Humanname
597766084CV3641711single nucleotide variantNM_001039780.4(CCNI2):c.265G>A (p.Ala89Thr)not specified [RCV004896064]likely benign5132747760132747760Humanname
597766088CV3641712single nucleotide variantNM_001039780.4(CCNI2):c.229C>G (p.Arg77Gly)not specified [RCV004896065]uncertain significance5132747724132747724Humanname
156397602CV2197302single nucleotide variantNM_001039780.4(CCNI2):c.755C>T (p.Pro252Leu)not specified [RCV004081050]uncertain significance5132750978132750978Humanname
156032488CV2239447single nucleotide variantNM_001039780.4(CCNI2):c.909G>C (p.Lys303Asn)not specified [RCV004114167]uncertain significance5132752100132752100Humanname
156174630CV2247689single nucleotide variantNM_001039780.4(CCNI2):c.705G>A (p.Met235Ile)not specified [RCV004115099]uncertain significance5132750928132750928Humanname
156132700CV2350182single nucleotide variantNM_001039780.4(CCNI2):c.668A>G (p.Tyr223Cys)not specified [RCV004200096]uncertain significance5132750891132750891Humanname
329352152CV2452093single nucleotide variantNM_001039780.4(CCNI2):c.916A>C (p.Thr306Pro)not specified [RCV004278815]uncertain significance5132752107132752107Humanname
329391460CV2452359single nucleotide variantNM_001039780.4(CCNI2):c.529A>G (p.Ile177Val)not specified [RCV004272684]uncertain significance5132748446132748446Humanname
329394467CV2469886single nucleotide variantNM_001039780.4(CCNI2):c.353A>T (p.Asp118Val)not specified [RCV004285357]uncertain significance5132747848132747848Humanname
329394469CV2469887single nucleotide variantNM_001039780.4(CCNI2):c.354C>A (p.Asp118Glu)not specified [RCV004285358]uncertain significance5132747849132747849Humanname
401782649CV2697140single nucleotide variantNM_001039780.4(CCNI2):c.329C>T (p.Pro110Leu)not specified [RCV004302134]uncertain significance5132747824132747824Humanname
401767516CV2727190single nucleotide variantNM_001039780.4(CCNI2):c.740T>C (p.Leu247Pro)not specified [RCV004327328]uncertain significance5132750963132750963Humanname
401890846CV2772227single nucleotide variantNM_001039780.4(CCNI2):c.950A>G (p.Glu317Gly)not specified [RCV004346867]uncertain significance5132752141132752141Humanname
401880821CV2789392single nucleotide variantNM_001039780.4(CCNI2):c.802C>A (p.Pro268Thr)not specified [RCV004360036]uncertain significance5132751993132751993Humanname
405741452CV3292677single nucleotide variantNM_001039780.4(CCNI2):c.307C>T (p.Pro103Ser)not specified [RCV004430766]uncertain significance5132747802132747802Humanname
405741461CV3292678single nucleotide variantNM_001039780.4(CCNI2):c.308C>G (p.Pro103Arg)not specified [RCV004430767]uncertain significance5132747803132747803Humanname
405741474CV3292680single nucleotide variantNM_001039780.4(CCNI2):c.475C>T (p.Arg159Trp)not specified [RCV004430769]uncertain significance5132748392132748392Humanname
405741480CV3292681single nucleotide variantNM_001039780.4(CCNI2):c.752C>T (p.Thr251Met)not specified [RCV004430770]uncertain significance5132750975132750975Humanname
405741497CV3292683single nucleotide variantNM_001039780.4(CCNI2):c.967T>C (p.Trp323Arg)not specified [RCV004430772]uncertain significance5132752158132752158Humanname
597766075CV3641708single nucleotide variantNM_001039780.4(CCNI2):c.680A>G (p.Tyr227Cys)not specified [RCV004896061]uncertain significance5132750903132750903Humanname
597766083CV3641710single nucleotide variantNM_001039780.4(CCNI2):c.451G>A (p.Glu151Lys)not specified [RCV004896063]uncertain significance5132748368132748368Humanname
597766092CV3641713single nucleotide variantNM_001039780.4(CCNI2):c.727C>G (p.Leu243Val)not specified [RCV004896066]uncertain significance5132750950132750950Humanname
598205251CV3939807single nucleotide variantNM_001039780.4(CCNI2):c.425C>G (p.Pro142Arg)not specified [RCV005314925]uncertain significance5132747920132747920Humanname
598205276CV3939810single nucleotide variantNM_001039780.4(CCNI2):c.627A>T (p.Glu209Asp)not specified [RCV005314928]uncertain significance5132749416132749416Humanname
156092449CV2216804single nucleotide variantNM_001039780.4(CCNI2):c.1027T>C (p.Cys343Arg)not specified [RCV004083241]uncertain significance5132752887132752887Humanname
329390865CV2455552single nucleotide variantNM_001039780.4(CCNI2):c.1091T>C (p.Phe364Ser)not specified [RCV004276807]uncertain significance5132752951132752951Humanname
405741433CV3292674single nucleotide variantNM_001039780.4(CCNI2):c.1025G>A (p.Ser342Asn)not specified [RCV004430763]uncertain significance5132752885132752885Humanname