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Variants search result for Homo sapiens
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41 records found for search term Klhl32
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
8582319CV116788single nucleotide variantNM_001286250.1(KLHL32):c.-66+11561C>ALung cancer [RCV000097311]uncertain significance69693658796936587Humanname
401775430CV2692371single nucleotide variantNM_052904.4(KLHL32):c.64G>A (p.Glu22Lys)not specified [RCV004310352]uncertain significance69697603796976037Humanname
401915881CV2820566single nucleotide variantNM_052904.4(KLHL32):c.753C>T (p.Val251=)not provided [RCV003428901]likely benign69711390897113908Humanname
405813644CV3276237single nucleotide variantNM_052904.4(KLHL32):c.92C>T (p.Ala31Val)not specified [RCV004409473]uncertain significance69697606596976065Humanname
156047443CV2216152single nucleotide variantNM_052904.4(KLHL32):c.164C>T (p.Ala55Val)not specified [RCV004097147]uncertain significance69697613796976137Humanname
401897911CV2769662single nucleotide variantNM_052904.4(KLHL32):c.104A>C (p.Gln35Pro)not specified [RCV004351590]uncertain significance69697607796976077Humanname
405813651CV3276234single nucleotide variantNM_052904.4(KLHL32):c.287C>T (p.Ala96Val)not specified [RCV004409470]uncertain significance69704157497041574Humanname
597640501CV3692464single nucleotide variantNM_052904.4(KLHL32):c.173C>G (p.Ala58Gly)not specified [RCV004941531]uncertain significance69697614696976146Humanname
597640530CV3692469single nucleotide variantNM_052904.4(KLHL32):c.112G>A (p.Asp38Asn)not specified [RCV004941536]uncertain significance69697608596976085Humanname
156374543CV2194626single nucleotide variantNM_052904.4(KLHL32):c.913A>G (p.Lys305Glu)not specified [RCV004082030]uncertain significance69711406897114068Humanname
155952575CV2264242single nucleotide variantNM_052904.4(KLHL32):c.964G>C (p.Ala322Pro)not specified [RCV004138171]uncertain significance69711411997114119Humanname
156087049CV2299086single nucleotide variantNM_052904.4(KLHL32):c.592C>T (p.Arg198Cys)not specified [RCV004152448]uncertain significance69708530697085306Humanname
156166315CV2319929single nucleotide variantNM_052904.4(KLHL32):c.353C>A (p.Ala118Glu)not specified [RCV004167807]uncertain significance69706466897064668Humanname
156089199CV2392044single nucleotide variantNM_052904.4(KLHL32):c.892A>G (p.Lys298Glu)not specified [RCV004237942]uncertain significance69711404797114047Humanname
401733402CV2685516single nucleotide variantNM_052904.4(KLHL32):c.710A>C (p.Asp237Ala)not specified [RCV004294536]uncertain significance69711386597113865Humanname
401754571CV2717438single nucleotide variantNM_052904.4(KLHL32):c.593G>A (p.Arg198His)not specified [RCV004330254]uncertain significance69708530797085307Humanname
401778012CV2718424single nucleotide variantNM_052904.4(KLHL32):c.493G>A (p.Asp165Asn)not specified [RCV004318244]uncertain significance69708520797085207Humanname
401878646CV2776871single nucleotide variantNM_052904.4(KLHL32):c.815A>G (p.Tyr272Cys)not specified [RCV004351697]uncertain significance69711397097113970Humanname
401892265CV2777375single nucleotide variantNM_052904.4(KLHL32):c.811A>G (p.Ile271Val)not specified [RCV004354381]uncertain significance69711396697113966Humanname
405813649CV3276235single nucleotide variantNM_052904.4(KLHL32):c.398A>G (p.His133Arg)not specified [RCV004409471]uncertain significance69706471397064713Humanname
405813646CV3276236single nucleotide variantNM_052904.4(KLHL32):c.880A>G (p.Ile294Val)not specified [RCV004409472]uncertain significance69711403597114035Humanname
597768794CV3692463single nucleotide variantNM_052904.4(KLHL32):c.898G>A (p.Glu300Lys)not specified [RCV004927566]uncertain significance69711405397114053Humanname
597640512CV3692466single nucleotide variantNM_052904.4(KLHL32):c.457C>T (p.Leu153Phe)not specified [RCV004941533]uncertain significance69708517197085171Humanname
156315759CV2192943single nucleotide variantNM_052904.4(KLHL32):c.1540C>T (p.Arg514Cys)not specified [RCV004069501]uncertain significance69713088397130883Humanname
155972121CV2228060single nucleotide variantNM_052904.4(KLHL32):c.1258T>C (p.Cys420Arg)not specified [RCV004096295]uncertain significance69711441397114413Humanname
155905618CV2303149single nucleotide variantNM_052904.4(KLHL32):c.1118C>G (p.Pro373Arg)not specified [RCV004156916]uncertain significance69711427397114273Humanname
156078953CV2318830single nucleotide variantNM_052904.4(KLHL32):c.1289A>G (p.Gln430Arg)not specified [RCV004175739]uncertain significance69711444497114444Humanname
329389072CV2448691single nucleotide variantNM_052904.4(KLHL32):c.1121G>A (p.Arg374His)not specified [RCV004259354]uncertain significance69711427697114276Humanname
401865497CV2755539single nucleotide variantNM_052904.4(KLHL32):c.1229G>A (p.Arg410His)not specified [RCV004340120]uncertain significance69711438497114384Humanname
401883074CV2788716single nucleotide variantNM_052904.4(KLHL32):c.1135G>T (p.Ala379Ser)not specified [RCV004361192]uncertain significance69711429097114290Humanname
405813657CV3276231single nucleotide variantNM_052904.4(KLHL32):c.1124G>C (p.Ser375Thr)not specified [RCV004409467]uncertain significance69711427997114279Humanname
405813655CV3276232single nucleotide variantNM_052904.4(KLHL32):c.1181G>A (p.Gly394Asp)not specified [RCV004409468]uncertain significance69711433697114336Humanname
405813653CV3276233single nucleotide variantNM_052904.4(KLHL32):c.1243A>G (p.Thr415Ala)not specified [RCV004409469]uncertain significance69711439897114398Humanname
407524979CV3448596single nucleotide variantNM_052904.4(KLHL32):c.1250A>G (p.Glu417Gly)not specified [RCV004631573]uncertain significance69711440597114405Humanname
407524982CV3448597single nucleotide variantNM_052904.4(KLHL32):c.1619C>G (p.Ser540Cys)not specified [RCV004631574]uncertain significance69713266597132665Humanname
597640494CV3692462single nucleotide variantNM_052904.4(KLHL32):c.1036G>C (p.Asp346His)not specified [RCV004941530]uncertain significance69711419197114191Humanname
597640506CV3692465single nucleotide variantNM_052904.4(KLHL32):c.1647A>G (p.Ile549Met)not specified [RCV004941532]uncertain significance69713269397132693Humanname
598182923CV3987394single nucleotide variantNM_052904.4(KLHL32):c.1637A>G (p.Asn546Ser)not specified [RCV005352813]uncertain significance69713268397132683Humanname
598221247CV3987395single nucleotide variantNM_052904.4(KLHL32):c.1477C>G (p.Gln493Glu)not specified [RCV005360780]uncertain significance69713082097130820Humanname
8626284CV81428single nucleotide variantNM_052904.3(KLHL32):c.1192G>A (p.Glu398Lys)Malignant melanoma [RCV000061506]not provided69711434797114347Humanname
8632216CV87422single nucleotide variantNM_052904.3(KLHL32):c.1003G>A (p.Gly335Arg)Malignant melanoma [RCV000067513]not provided69711415897114158Humanname