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35 records found for search term Ppil6
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401877136CV2790061single nucleotide variantNM_173672.5(PPIL6):c.689-2876A>Tnot specified [RCV004364011]uncertain significance6109403046109403046Humanname
405794471CV3366369single nucleotide variantNM_173672.5(PPIL6):c.689-2888G>Cnot specified [RCV004507071]uncertain significance6109403058109403058Humanname
407482819CV3471440single nucleotide variantNM_173672.5(PPIL6):c.689-2915A>Cnot specified [RCV004664838]uncertain significance6109403085109403085Humanname
156307243CV2335410single nucleotide variantNM_173672.5(PPIL6):c.11C>T (p.Pro4Leu)not specified [RCV004186964]uncertain significance6109440580109440580Humanname
329388122CV2468606single nucleotide variantNM_173672.5(PPIL6):c.26C>T (p.Pro9Leu)not specified [RCV004278166]uncertain significance6109440565109440565Humanname
405794462CV3366366single nucleotide variantNM_173672.5(PPIL6):c.14A>G (p.Gln5Arg)not specified [RCV004507068]uncertain significance6109440577109440577Humanname
405794468CV3366368single nucleotide variantNM_173672.5(PPIL6):c.26C>A (p.Pro9His)not specified [RCV004507070]uncertain significance6109440565109440565Humanname
598160319CV3897390single nucleotide variantNM_173672.5(PPIL6):c.23G>A (p.Gly8Glu)not specified [RCV005260957]uncertain significance6109440568109440568Humanname
329376322CV2425072single nucleotide variantNM_173672.5(PPIL6):c.68C>T (p.Pro23Leu)not specified [RCV004248968]uncertain significance6109440523109440523Humanname
329372785CV2428650single nucleotide variantNM_173672.5(PPIL6):c.50C>A (p.Pro17Gln)not specified [RCV004255450]likely benign6109440541109440541Humanname
329373769CV2434581single nucleotide variantNM_173672.5(PPIL6):c.95T>A (p.Phe32Tyr)not specified [RCV004254279]uncertain significance6109440496109440496Humanname
407482812CV3471439single nucleotide variantNM_173672.5(PPIL6):c.64C>T (p.Arg22Trp)not specified [RCV004664837]uncertain significance6109440527109440527Humanname
597757812CV3591250single nucleotide variantNM_173672.5(PPIL6):c.31C>T (p.His11Tyr)not specified [RCV004848399]uncertain significance6109440560109440560Humanname
156102218CV2367747single nucleotide variantNM_173672.5(PPIL6):c.133G>A (p.Glu45Lys)not specified [RCV004213705]uncertain significance6109440458109440458Humanname
401774281CV2727791single nucleotide variantNM_173672.5(PPIL6):c.146A>G (p.Asn49Ser)not specified [RCV004323817]likely benign6109436189109436189Humanname
401862393CV2775281single nucleotide variantNM_173672.5(PPIL6):c.263C>T (p.Ser88Phe)not specified [RCV004348401]uncertain significance6109431314109431314Humanname
405794465CV3366367single nucleotide variantNM_173672.5(PPIL6):c.199G>A (p.Ala67Thr)not specified [RCV004507069]uncertain significance6109436136109436136Humanname
407482824CV3471442single nucleotide variantNM_173672.5(PPIL6):c.184C>T (p.Pro62Ser)not specified [RCV004664839]uncertain significance6109436151109436151Humanname
598160313CV3897389single nucleotide variantNM_173672.5(PPIL6):c.284A>C (p.Asn95Thr)not specified [RCV005260956]uncertain significance6109431293109431293Humanname
156159822CV2236267single nucleotide variantNM_173672.5(PPIL6):c.430G>T (p.Val144Leu)not specified [RCV004107967]uncertain significance6109427147109427147Humanname
156114906CV2273246single nucleotide variantNM_173672.5(PPIL6):c.696C>A (p.Asn232Lys)not specified [RCV004132041]uncertain significance6109400163109400163Humanname
156006214CV2281800single nucleotide variantNM_173672.5(PPIL6):c.740A>G (p.Asn247Ser)not specified [RCV004147933]uncertain significance6109400119109400119Humanname
156271883CV2308666single nucleotide variantNM_173672.5(PPIL6):c.364G>A (p.Ala122Thr)not specified [RCV004167215]uncertain significance6109431213109431213Humanname
156166323CV2315225single nucleotide variantNM_173672.5(PPIL6):c.833T>C (p.Ile278Thr)not specified [RCV004165392]uncertain significance6109392929109392929Humanname
156136436CV2364944single nucleotide variantNM_173672.5(PPIL6):c.899T>C (p.Met300Thr)not specified [RCV004222239]uncertain significance6109392863109392863Humanname
156006098CV2401161single nucleotide variantNM_173672.5(PPIL6):c.463A>G (p.Ile155Val)not specified [RCV004245719]uncertain significance6109427114109427114Humanname
401864778CV2778039single nucleotide variantNM_173672.5(PPIL6):c.760G>A (p.Gly254Arg)not specified [RCV004347993]uncertain significance6109400099109400099Humanname
401899978CV2780140single nucleotide variantNM_173672.5(PPIL6):c.748C>T (p.Arg250Cys)not specified [RCV004355796]uncertain significance6109400111109400111Humanname
405794474CV3366370single nucleotide variantNM_173672.5(PPIL6):c.694A>G (p.Asn232Asp)not specified [RCV004507072]uncertain significance6109400165109400165Humanname
405794476CV3366371single nucleotide variantNM_173672.5(PPIL6):c.835G>A (p.Glu279Lys)not specified [RCV004507073]uncertain significance6109392927109392927Humanname
405854748CV3394863single nucleotide variantNM_173672.5(PPIL6):c.451G>A (p.Asp151Asn)not provided [RCV004555004]uncertain significance6109427126109427126Humanname
407529621CV3471441single nucleotide variantNM_173672.5(PPIL6):c.352A>C (p.Ile118Leu)not specified [RCV004656134]uncertain significance6109431225109431225Humanname
597757808CV3591249single nucleotide variantNM_173672.5(PPIL6):c.725T>C (p.Val242Ala)not specified [RCV004848398]uncertain significance6109400134109400134Humanname
597757817CV3591251single nucleotide variantNM_173672.5(PPIL6):c.673G>T (p.Gly225Cys)not specified [RCV004848400]uncertain significance6109419202109419202Humanname
598160323CV3897391single nucleotide variantNM_173672.5(PPIL6):c.657T>G (p.Asn219Lys)not specified [RCV005260958]uncertain significance6109419218109419218Humanname