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Variants search result for Homo sapiens
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40 records found for search term Ccdc121
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
329388440CV2437410single nucleotide variantNM_024584.5(CCDC121):c.-25G>Cnot specified [RCV004256279]uncertain significance22762782427627824Humanname
405754901CV3302818single nucleotide variantNM_024584.5(CCDC121):c.-97G>Cnot specified [RCV004432678]likely benign22762789627627896Humanname
405754907CV3302819single nucleotide variantNM_024584.5(CCDC121):c.-65A>Gnot specified [RCV004432679]uncertain significance22762786427627864Humanname
405754914CV3302820single nucleotide variantNM_024584.5(CCDC121):c.-47A>Tnot specified [RCV004432680]uncertain significance22762784627627846Humanname
598177071CV3950623single nucleotide variantNM_024584.5(CCDC121):c.-116T>Cnot specified [RCV005310147]uncertain significance22762791527627915Humanname
156321126CV2197495single nucleotide variantNM_024584.5(CCDC121):c.-119+323A>Cnot specified [RCV004081223]likely benign22762862727628627Humanname
155992538CV2281219single nucleotide variantNM_024584.5(CCDC121):c.-119+421G>Anot specified [RCV004147468]likely benign22762852927628529Humanname
156035936CV2303612single nucleotide variantNM_024584.5(CCDC121):c.-119+424C>Gnot specified [RCV004161697]uncertain significance22762852627628526Humanname
156062701CV2316601single nucleotide variantNM_024584.5(CCDC121):c.-119+463C>Gnot specified [RCV004171849]uncertain significance22762848727628487Humanname
156339802CV2367698single nucleotide variantNM_024584.5(CCDC121):c.-119+337C>Anot specified [RCV004211613]uncertain significance22762861327628613Humanname
405754882CV3302815single nucleotide variantNM_024584.5(CCDC121):c.-119+292C>Gnot specified [RCV004432675]uncertain significance22762865827628658Humanname
405754895CV3302817single nucleotide variantNM_024584.5(CCDC121):c.-119+385C>Gnot specified [RCV004432677]uncertain significance22762856527628565Humanname
405754926CV3302822single nucleotide variantNM_024584.5(CCDC121):c.-119+257G>Anot specified [RCV004432682]uncertain significance22762869327628693Humanname
407481329CV3418209single nucleotide variantNM_024584.5(CCDC121):c.-119+287C>Tnot specified [RCV004602818]uncertain significance22762866327628663Humanname
407482015CV3418211single nucleotide variantNM_024584.5(CCDC121):c.-119+496G>Anot specified [RCV004609814]likely benign22762845427628454Humanname
597692413CV3638031single nucleotide variantNM_024584.5(CCDC121):c.-119+476C>Gnot specified [RCV004900971]uncertain significance22762847427628474Humanname
401861215CV2769579single nucleotide variantNM_024584.5(CCDC121):c.14A>G (p.Asn5Ser)not specified [RCV004351226]uncertain significance22762778627627786Humanname
405754920CV3302821single nucleotide variantNM_024584.5(CCDC121):c.24A>G (p.Ile8Met)not specified [RCV004432681]uncertain significance22762777627627776Humanname
329379171CV2460200single nucleotide variantNM_024584.5(CCDC121):c.85A>G (p.Lys29Glu)not specified [RCV004273296]uncertain significance22762771527627715Humanname
597786414CV3638030single nucleotide variantNM_024584.5(CCDC121):c.83A>G (p.Glu28Gly)not specified [RCV004900970]uncertain significance22762771727627717Humanname
598177060CV3950621single nucleotide variantNM_024584.5(CCDC121):c.80G>C (p.Arg27Pro)not specified [RCV005310145]uncertain significance22762772027627720Humanname
156369195CV2193914single nucleotide variantNM_024584.5(CCDC121):c.199G>A (p.Glu67Lys)not specified [RCV004074646]uncertain significance22762760127627601Humanname
156072362CV2251484single nucleotide variantNM_024584.5(CCDC121):c.230C>A (p.Ser77Tyr)not specified [RCV004117458]uncertain significance22762757027627570Humanname
155972431CV2334332single nucleotide variantNM_024584.5(CCDC121):c.133A>G (p.Asn45Asp)not specified [RCV004188310]uncertain significance22762766727627667Humanname
401874292CV2773740single nucleotide variantNM_024584.5(CCDC121):c.200A>G (p.Glu67Gly)not specified [RCV004356411]uncertain significance22762760027627600Humanname
597760723CV3638027single nucleotide variantNM_024584.5(CCDC121):c.236A>G (p.Tyr79Cys)not specified [RCV004894832]uncertain significance22762756427627564Humanname
156098260CV2253253single nucleotide variantNM_024584.5(CCDC121):c.677G>C (p.Arg226Thr)not specified [RCV004122794]uncertain significance22762712327627123Humanname
156295630CV2297489single nucleotide variantNM_024584.5(CCDC121):c.474C>A (p.Ser158Arg)not specified [RCV004153420]uncertain significance22762732627627326Humanname
156162924CV2323568single nucleotide variantNM_024584.5(CCDC121):c.811A>C (p.Thr271Pro)not specified [RCV004165764]uncertain significance22762698927626989Humanname
155922654CV2340656single nucleotide variantNM_024584.5(CCDC121):c.634C>G (p.Gln212Glu)not specified [RCV004190329]uncertain significance22762716627627166Humanname
156182791CV2353184single nucleotide variantNM_024584.5(CCDC121):c.488G>C (p.Arg163Thr)not specified [RCV004203655]uncertain significance22762731227627312Humanname
329386468CV2456030single nucleotide variantNM_024584.5(CCDC121):c.406G>T (p.Ala136Ser)not specified [RCV004272934]uncertain significance22762739427627394Humanname
329386470CV2456031single nucleotide variantNM_024584.5(CCDC121):c.407C>T (p.Ala136Val)not specified [RCV004272935]uncertain significance22762739327627393Humanname
405754888CV3302816single nucleotide variantNM_024584.5(CCDC121):c.778G>A (p.Val260Ile)not specified [RCV004432676]uncertain significance22762702227627022Humanname
407483243CV3418210single nucleotide variantNM_024584.5(CCDC121):c.541A>C (p.Lys181Gln)not specified [RCV004602819]uncertain significance22762725927627259Humanname
407454336CV3418212single nucleotide variantNM_024584.5(CCDC121):c.644A>C (p.Lys215Thr)not specified [RCV004609815]uncertain significance22762715627627156Humanname
597786395CV3638025single nucleotide variantNM_024584.5(CCDC121):c.499A>G (p.Lys167Glu)not specified [RCV004900966]uncertain significance22762730127627301Humanname
597786401CV3638026single nucleotide variantNM_024584.5(CCDC121):c.430G>A (p.Ala144Thr)not specified [RCV004900967]uncertain significance22762737027627370Humanname
597786405CV3638028single nucleotide variantNM_024584.5(CCDC121):c.808G>A (p.Gly270Ser)not specified [RCV004900968]uncertain significance22762699227626992Humanname
598177067CV3950622single nucleotide variantNM_024584.5(CCDC121):c.652G>C (p.Ala218Pro)not specified [RCV005310146]uncertain significance22762714827627148Humanname