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Variants search result for Homo sapiens
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70 records found for search term Kif2b
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156293359CV2293048single nucleotide variantNM_032559.5(KIF2B):c.29C>G (p.Ser10Cys)not specified [RCV004148800]uncertain significance175382306253823062Humanname
156053259CV2360999single nucleotide variantNM_032559.5(KIF2B):c.40T>C (p.Ser14Pro)not specified [RCV004216196]uncertain significance175382307353823073Humanname
401723703CV2725001single nucleotide variantNM_032559.5(KIF2B):c.95T>C (p.Val32Ala)not specified [RCV004319760]uncertain significance175382312853823128Humanname
597630496CV3695188single nucleotide variantNM_032559.5(KIF2B):c.84G>C (p.Glu28Asp)not specified [RCV004939504]uncertain significance175382311753823117Humanname
156366191CV2203283single nucleotide variantNM_032559.5(KIF2B):c.203G>T (p.Gly68Val)not specified [RCV004071318]uncertain significance175382323653823236Humanname
155983463CV2273081single nucleotide variantNM_032559.5(KIF2B):c.257C>T (p.Ala86Val)not specified [RCV004137727]uncertain significance175382329053823290Humanname
597768276CV3695191single nucleotide variantNM_032559.5(KIF2B):c.244G>A (p.Ala82Thr)not specified [RCV004927449]uncertain significance175382327753823277Humanname
8628028CV83172single nucleotide variantNM_032559.4(KIF2B):c.1332C>T (p.Ser444=)Malignant melanoma [RCV000063252]not provided175382436553824365Humanname
156176678CV2205341single nucleotide variantNM_032559.5(KIF2B):c.674A>G (p.Gln225Arg)not specified [RCV004079955]uncertain significance175382370753823707Humanname
156132954CV2235368single nucleotide variantNM_032559.5(KIF2B):c.448C>T (p.Leu150Phe)not specified [RCV004109433]uncertain significance175382348153823481Humanname
156096366CV2253114single nucleotide variantNM_032559.5(KIF2B):c.638G>T (p.Arg213Leu)not specified [RCV004120896]uncertain significance175382367153823671Humanname
155977694CV2266436single nucleotide variantNM_032559.5(KIF2B):c.488G>A (p.Arg163His)not specified [RCV004131019]uncertain significance175382352153823521Humanname
156072691CV2267541single nucleotide variantNM_032559.5(KIF2B):c.833T>C (p.Leu278Ser)not specified [RCV004135960]uncertain significance175382386653823866Humanname
155968527CV2391471single nucleotide variantNM_032559.5(KIF2B):c.311C>T (p.Ser104Leu)not specified [RCV004239861]uncertain significance175382334453823344Humanname
329367541CV2427434single nucleotide variantNM_032559.5(KIF2B):c.947A>G (p.Asp316Gly)not specified [RCV004248286]uncertain significance175382398053823980Humanname
329360887CV2439856single nucleotide variantNM_032559.5(KIF2B):c.980G>T (p.Gly327Val)not specified [RCV004257898]uncertain significance175382401353824013Humanname
401744714CV2681108single nucleotide variantNM_032559.5(KIF2B):c.502C>A (p.Gln168Lys)not specified [RCV004296166]uncertain significance175382353553823535Humanname
401761001CV2695241single nucleotide variantNM_032559.5(KIF2B):c.944G>A (p.Gly315Glu)not specified [RCV004303374]uncertain significance175382397753823977Humanname
401761059CV2695262single nucleotide variantNM_032559.5(KIF2B):c.613G>C (p.Val205Leu)not specified [RCV004303393]uncertain significance175382364653823646Humanname
401763190CV2707572single nucleotide variantNM_032559.5(KIF2B):c.385G>T (p.Asp129Tyr)not specified [RCV004306517]uncertain significance175382341853823418Humanname
401761895CV2713937single nucleotide variantNM_032559.5(KIF2B):c.328C>G (p.Arg110Gly)not specified [RCV004315361]uncertain significance175382336153823361Humanname
401881620CV2784751single nucleotide variantNM_032559.5(KIF2B):c.443C>T (p.Pro148Leu)not specified [RCV004352551]uncertain significance175382347653823476Humanname
405653088CV3268948single nucleotide variantNM_032559.5(KIF2B):c.311C>G (p.Ser104Trp)not specified [RCV004414202]uncertain significance175382334453823344Humanname
405653083CV3268950single nucleotide variantNM_032559.5(KIF2B):c.523G>T (p.Ala175Ser)not specified [RCV004414204]uncertain significance175382355653823556Humanname
405653081CV3268951single nucleotide variantNM_032559.5(KIF2B):c.760G>A (p.Asp254Asn)not specified [RCV004414205]uncertain significance175382379353823793Humanname
405653079CV3268952single nucleotide variantNM_032559.5(KIF2B):c.881A>G (p.Lys294Arg)not specified [RCV004414206]uncertain significance175382391453823914Humanname
405653077CV3268953single nucleotide variantNM_032559.5(KIF2B):c.941G>A (p.Gly314Asp)not specified [RCV004414207]uncertain significance175382397453823974Humanname
407524712CV3452159single nucleotide variantNM_032559.5(KIF2B):c.636T>A (p.His212Gln)not specified [RCV004631474]uncertain significance175382366953823669Humanname
407469615CV3452162single nucleotide variantNM_032559.5(KIF2B):c.626C>T (p.Pro209Leu)not specified [RCV004636895]uncertain significance175382365953823659Humanname
407469617CV3452163single nucleotide variantNM_032559.5(KIF2B):c.929C>T (p.Thr310Met)not specified [RCV004636896]uncertain significance175382396253823962Humanname
407469619CV3452164single nucleotide variantNM_032559.5(KIF2B):c.367A>G (p.Asn123Asp)not specified [RCV004636897]uncertain significance175382340053823400Humanname
597630503CV3695189single nucleotide variantNM_032559.5(KIF2B):c.956G>T (p.Gly319Val)not specified [RCV004939505]uncertain significance175382398953823989Humanname
597768280CV3695193single nucleotide variantNM_032559.5(KIF2B):c.932A>C (p.Tyr311Ser)not specified [RCV004927450]uncertain significance175382396553823965Humanname
597630873CV3695196single nucleotide variantNM_032559.5(KIF2B):c.515C>T (p.Ala172Val)not specified [RCV004939509]uncertain significance175382354853823548Humanname
598272571CV3991017single nucleotide variantNM_032559.5(KIF2B):c.959C>G (p.Thr320Arg)not specified [RCV005350520]likely benign175382399253823992Humanname
15168624CV715568single nucleotide variantNM_032559.5(KIF2B):c.769C>T (p.Arg257Cys)not provided [RCV000971652]benign175382380253823802Humanname
156087471CV2205804single nucleotide variantNM_032559.5(KIF2B):c.1782G>C (p.Glu594Asp)not specified [RCV004075849]uncertain significance175382481553824815Humanname
155918732CV2206072single nucleotide variantNM_032559.5(KIF2B):c.1048C>T (p.Leu350Phe)not specified [RCV004078483]uncertain significance175382408153824081Humanname
156335483CV2228399single nucleotide variantNM_032559.5(KIF2B):c.1703A>G (p.His568Arg)not specified [RCV004098377]uncertain significance175382473653824736Humanname
156181220CV2246177single nucleotide variantNM_032559.5(KIF2B):c.1822G>A (p.Asp608Asn)not specified [RCV004107648]uncertain significance175382485553824855Humanname
156369052CV2263255single nucleotide variantNM_032559.5(KIF2B):c.1364C>G (p.Ala455Gly)not specified [RCV004131754]uncertain significance175382439753824397Humanname
155961962CV2285596single nucleotide variantNM_032559.5(KIF2B):c.1753C>T (p.Pro585Ser)not specified [RCV004141466]uncertain significance175382478653824786Humanname
156011242CV2291123single nucleotide variantNM_032559.5(KIF2B):c.1079A>T (p.Tyr360Phe)not specified [RCV004151646]uncertain significance175382411253824112Humanname
156144897CV2292331single nucleotide variantNM_032559.5(KIF2B):c.1258G>A (p.Ala420Thr)not specified [RCV004150146]uncertain significance175382429153824291Humanname
156038414CV2332628single nucleotide variantNM_032559.5(KIF2B):c.1655G>A (p.Arg552His)not specified [RCV004189308]uncertain significance175382468853824688Humanname
156069972CV2355923single nucleotide variantNM_032559.5(KIF2B):c.1223A>G (p.Asn408Ser)not specified [RCV004201307]uncertain significance175382425653824256Humanname
156203512CV2400431single nucleotide variantNM_032559.5(KIF2B):c.1231C>T (p.Arg411Trp)not specified [RCV004244477]uncertain significance175382426453824264Humanname
405652580CV3268938single nucleotide variantNM_032559.5(KIF2B):c.1100T>C (p.Leu367Ser)not specified [RCV004414192]uncertain significance175382413353824133Humanname
405652582CV3268939single nucleotide variantNM_032559.5(KIF2B):c.1258G>T (p.Ala420Ser)not specified [RCV004414193]uncertain significance175382429153824291Humanname
405653102CV3268940single nucleotide variantNM_032559.5(KIF2B):c.1259C>T (p.Ala420Val)not specified [RCV004414194]uncertain significance175382429253824292Humanname
405653100CV3268941single nucleotide variantNM_032559.5(KIF2B):c.1384C>T (p.Arg462Trp)not specified [RCV004414195]uncertain significance175382441753824417Humanname
405653099CV3268942single nucleotide variantNM_032559.5(KIF2B):c.1468C>T (p.Pro490Ser)not specified [RCV004414196]likely benign175382450153824501Humanname
405653097CV3268943single nucleotide variantNM_032559.5(KIF2B):c.1631A>G (p.Asn544Ser)not specified [RCV004414197]uncertain significance175382466453824664Humanname
405653095CV3268944single nucleotide variantNM_032559.5(KIF2B):c.1655G>C (p.Arg552Pro)not specified [RCV004414198]uncertain significance175382468853824688Humanname
405653093CV3268945single nucleotide variantNM_032559.5(KIF2B):c.1918C>T (p.Arg640Trp)not specified [RCV004414199]uncertain significance175382495153824951Humanname
405653091CV3268946single nucleotide variantNM_032559.5(KIF2B):c.1962G>C (p.Glu654Asp)not specified [RCV004414200]uncertain significance175382499553824995Humanname
405653089CV3268947single nucleotide variantNM_032559.5(KIF2B):c.1979A>G (p.Lys660Arg)not specified [RCV004414201]uncertain significance175382501253825012Humanname
407524715CV3452160single nucleotide variantNM_032559.5(KIF2B):c.1950T>A (p.Asp650Glu)not specified [RCV004631475]uncertain significance175382498353824983Humanname
407496001CV3452161single nucleotide variantNM_032559.5(KIF2B):c.1951G>T (p.Ala651Ser)not specified [RCV004621702]uncertain significance175382498453824984Humanname
597630509CV3695192single nucleotide variantNM_032559.5(KIF2B):c.1163G>T (p.Gly388Val)not specified [RCV004939506]uncertain significance175382419653824196Humanname
597630515CV3695194single nucleotide variantNM_032559.5(KIF2B):c.1232G>A (p.Arg411Gln)not specified [RCV004939507]uncertain significance175382426553824265Humanname
597630522CV3695195single nucleotide variantNM_032559.5(KIF2B):c.1042C>A (p.Leu348Met)not specified [RCV004939508]uncertain significance175382407553824075Humanname
598220538CV3991015single nucleotide variantNM_032559.5(KIF2B):c.1810C>G (p.Leu604Val)not specified [RCV005360681]uncertain significance175382484353824843Humanname
598272564CV3991016single nucleotide variantNM_032559.5(KIF2B):c.1548G>T (p.Met516Ile)not specified [RCV005350519]uncertain significance175382458153824581Humanname
598272576CV3991018single nucleotide variantNM_032559.5(KIF2B):c.1411A>T (p.Ile471Phe)not specified [RCV005350521]uncertain significance175382444453824444Humanname
598248480CV3991019single nucleotide variantNM_032559.5(KIF2B):c.1885G>A (p.Gly629Arg)not specified [RCV005366238]uncertain significance175382491853824918Humanname
15103751CV727294single nucleotide variantNM_032559.5(KIF2B):c.1654C>T (p.Arg552Cys)not provided [RCV000892741]benign175382468753824687Humanname
8628027CV83171single nucleotide variantNM_032559.4(KIF2B):c.1331C>T (p.Ser444Phe)Malignant melanoma [RCV000063251]not provided175382436453824364Humanname
8628029CV83173single nucleotide variantNM_032559.4(KIF2B):c.1403G>A (p.Gly468Glu)Malignant melanoma [RCV000063253]not provided175382443653824436Humanname
8636252CV91476single nucleotide variantNM_032559.4(KIF2B):c.1861G>A (p.Glu621Lys)Malignant melanoma [RCV000071574]not provided175382489453824894Humanname