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Variants search result for Homo sapiens
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22 records found for search term Pla2g2e
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155904820CV2349591single nucleotide variantNM_014589.3(PLA2G2E):c.86A>G (p.Glu29Gly)not specified [RCV004204015]uncertain significance11992271019922710Humanname
156061160CV2380207single nucleotide variantNM_014589.3(PLA2G2E):c.43G>A (p.Ala15Thr)not specified [RCV004224573]uncertain significance11992275319922753Humanname
401862920CV2762372single nucleotide variantNM_014589.3(PLA2G2E):c.55G>A (p.Gly19Arg)not specified [RCV004335483]uncertain significance11992274119922741Humanname
405656484CV3375978single nucleotide variantNM_014589.3(PLA2G2E):c.49G>C (p.Val17Leu)not specified [RCV004511448]uncertain significance11992274719922747Humanname
405656385CV3375979single nucleotide variantNM_014589.3(PLA2G2E):c.59A>C (p.Asn20Thr)not specified [RCV004511449]uncertain significance11992273719922737Humanname
407512782CV3460660single nucleotide variantNM_014589.3(PLA2G2E):c.85G>A (p.Glu29Lys)not specified [RCV004648545]uncertain significance11992271119922711Humanname
156063584CV2228783single nucleotide variantNM_014589.3(PLA2G2E):c.271C>G (p.Arg91Gly)not specified [RCV004095034]uncertain significance11992231319922313Humanname
156011667CV2291168single nucleotide variantNM_014589.3(PLA2G2E):c.178T>G (p.Trp60Gly)not specified [RCV004153472]uncertain significance11992261819922618Humanname
156167027CV2398995single nucleotide variantNM_014589.3(PLA2G2E):c.253C>T (p.Leu85Phe)not specified [RCV004245300]uncertain significance11992233119922331Humanname
401724368CV2714816single nucleotide variantNM_014589.3(PLA2G2E):c.190G>A (p.Ala64Thr)not specified [RCV004320376]uncertain significance11992239419922394Humanname
405656489CV3375977single nucleotide variantNM_014589.3(PLA2G2E):c.258C>G (p.Phe86Leu)not specified [RCV004511447]uncertain significance11992232619922326Humanname
407470221CV3460659single nucleotide variantNM_014589.3(PLA2G2E):c.197A>G (p.Asp66Gly)not specified [RCV004661964]uncertain significance11992238719922387Humanname
597704871CV3569638single nucleotide variantNM_014589.3(PLA2G2E):c.158G>C (p.Trp53Ser)not specified [RCV004840181]uncertain significance11992263819922638Humanname
597704900CV3569641single nucleotide variantNM_014589.3(PLA2G2E):c.121G>A (p.Asp41Asn)not specified [RCV004840184]uncertain significance11992267519922675Humanname
597704908CV3569642single nucleotide variantNM_014589.3(PLA2G2E):c.257T>C (p.Phe86Ser)not specified [RCV004840185]uncertain significance11992232719922327Humanname
598169469CV4000220single nucleotide variantNM_014589.3(PLA2G2E):c.139G>A (p.Gly47Ser)not specified [RCV005392078]uncertain significance11992265719922657Humanname
598169473CV4000221single nucleotide variantNM_014589.3(PLA2G2E):c.193C>T (p.His65Tyr)not specified [RCV005392079]uncertain significance11992239119922391Humanname
598169476CV4000222single nucleotide variantNM_014589.3(PLA2G2E):c.203G>A (p.Cys68Tyr)not specified [RCV005392080]uncertain significance11992238119922381Humanname
155904981CV2349645single nucleotide variantNM_014589.3(PLA2G2E):c.355A>G (p.Asn119Asp)not specified [RCV004204064]uncertain significance11992038119920381Humanname
329378436CV2446959single nucleotide variantNM_014589.3(PLA2G2E):c.349C>T (p.Arg117Cys)not specified [RCV004257803]uncertain significance11992038719920387Humanname
329362818CV2449377single nucleotide variantNM_014589.3(PLA2G2E):c.328A>G (p.Lys110Glu)not specified [RCV004266538]uncertain significance11992040819920408Humanname
597704893CV3569640single nucleotide variantNM_014589.3(PLA2G2E):c.334G>A (p.Ala112Thr)not specified [RCV004840183]uncertain significance11992040219920402Humanname