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22 records found for search term Pik3ip1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156114606CV2349220single nucleotide variantNM_052880.5(PIK3IP1):c.14G>T (p.Trp5Leu)not specified [RCV004199173]uncertain significance223129233131292331Humanname
405791072CV3372626single nucleotide variantNM_052880.5(PIK3IP1):c.25T>C (p.Phe9Leu)not specified [RCV004505878]uncertain significance223129232031292320Humanname
155912297CV2235556single nucleotide variantNM_052880.5(PIK3IP1):c.36C>A (p.Ser12Arg)not specified [RCV004109586]uncertain significance223129230931292309Humanname
156295206CV2239621single nucleotide variantNM_052880.5(PIK3IP1):c.35G>A (p.Ser12Asn)not specified [RCV004108179]uncertain significance223129231031292310Humanname
407512049CV3463614single nucleotide variantNM_052880.5(PIK3IP1):c.43C>A (p.Leu15Ile)not specified [RCV004648258]uncertain significance223129230231292302Humanname
155984884CV2247809single nucleotide variantNM_052880.5(PIK3IP1):c.181G>C (p.Val61Leu)not specified [RCV004121273]uncertain significance223129118631291186Humanname
155951593CV2264121single nucleotide variantNM_052880.5(PIK3IP1):c.235G>A (p.Gly79Arg)not specified [RCV004136281]uncertain significance223129103731291037Humanname
405791178CV3372625single nucleotide variantNM_052880.5(PIK3IP1):c.190G>A (p.Ala64Thr)not specified [RCV004505877]uncertain significance223129108231291082Humanname
597740614CV3575896single nucleotide variantNM_052880.5(PIK3IP1):c.181G>A (p.Val61Met)not specified [RCV004844529]uncertain significance223129118631291186Humanname
401866992CV2792576single nucleotide variantNM_052880.5(PIK3IP1):c.686A>G (p.Glu229Gly)not specified [RCV004363608]uncertain significance223128319031283190Humanname
405867019CV2842530single nucleotide variantNM_052880.5(PIK3IP1):c.463C>T (p.Arg155Trp)EBV-positive nodal T- and NK-cell lymphoma [RCV004557887]likely benign223128954431289544Humanname
405790977CV3372627single nucleotide variantNM_052880.5(PIK3IP1):c.638T>C (p.Met213Thr)not specified [RCV004505879]uncertain significance223128323831283238Humanname
405790904CV3372628single nucleotide variantNM_052880.5(PIK3IP1):c.689T>C (p.Ile230Thr)not specified [RCV004505880]uncertain significance223128318731283187Humanname
405790803CV3372629single nucleotide variantNM_052880.5(PIK3IP1):c.748G>A (p.Gly250Ser)not specified [RCV004505881]uncertain significance223128312831283128Humanname
405790800CV3372630single nucleotide variantNM_052880.5(PIK3IP1):c.760C>T (p.Leu254Phe)not specified [RCV004505882]uncertain significance223128311631283116Humanname
405791247CV3372631single nucleotide variantNM_052880.5(PIK3IP1):c.767G>A (p.Gly256Asp)not specified [RCV004505883]uncertain significance223128310931283109Humanname
407512045CV3463613single nucleotide variantNM_052880.5(PIK3IP1):c.745G>A (p.Glu249Lys)not specified [RCV004648257]uncertain significance223128313131283131Humanname
597740618CV3575897single nucleotide variantNM_052880.5(PIK3IP1):c.456C>G (p.Ile152Met)not specified [RCV004844530]uncertain significance223128955131289551Humanname
597767352CV3575898single nucleotide variantNM_052880.5(PIK3IP1):c.595G>A (p.Asp199Asn)not specified [RCV004850449]uncertain significance223128328131283281Humanname
597740622CV3575899single nucleotide variantNM_052880.5(PIK3IP1):c.738C>A (p.Asp246Glu)not specified [RCV004844531]uncertain significance223128313831283138Humanname
598272662CV4006668single nucleotide variantNM_052880.5(PIK3IP1):c.419G>T (p.Arg140Leu)not specified [RCV005389445]uncertain significance223128958831289588Humanname
598272666CV4006669single nucleotide variantNM_052880.5(PIK3IP1):c.457A>C (p.Ser153Arg)not specified [RCV005389446]uncertain significance223128955031289550Humanname