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Variants search result for Homo sapiens
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17 records found for search term Lypla1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156102912CV2400168single nucleotide variantNM_006330.4(LYPLA1):c.7G>A (p.Gly3Ser)not specified [RCV004242969]uncertain significance85410181754101817Humanname
156086896CV2295372single nucleotide variantNM_006330.4(LYPLA1):c.43C>T (p.Pro15Ser)not specified [RCV004158721]uncertain significance85410178154101781Humanname
401731117CV2674266single nucleotide variantNM_006330.4(LYPLA1):c.37A>G (p.Ile13Val)not specified [RCV004289150]uncertain significance85410178754101787Humanname
401924011CV2821087single nucleotide variantNM_006330.4(LYPLA1):c.510C>T (p.His170=)not provided [RCV003435494]likely benign85405114154051141Humanname
405816154CV3280985single nucleotide variantNM_006330.4(LYPLA1):c.98C>T (p.Thr33Ile)not specified [RCV004411039]uncertain significance85410091154100911Humanname
156333119CV2220787single nucleotide variantNM_006330.4(LYPLA1):c.145A>G (p.Ile49Val)not specified [RCV004092235]uncertain significance85406577054065770Humanname
156092280CV2256658single nucleotide variantNM_006330.4(LYPLA1):c.422C>G (p.Ala141Gly)not specified [RCV004118840]uncertain significance85405269554052695Humanname
156214989CV2257532single nucleotide variantNM_006330.4(LYPLA1):c.625A>T (p.Ser209Cys)not specified [RCV004125587]uncertain significance85405102654051026Humanname
155910579CV2303625single nucleotide variantNM_006330.4(LYPLA1):c.322A>G (p.Ile108Val)not specified [RCV004161707]uncertain significance85405509854055098Humanname
156260798CV2314644single nucleotide variantNM_006330.4(LYPLA1):c.308A>T (p.Glu103Val)not specified [RCV004170801]uncertain significance85405511254055112Humanname
329370933CV2431815single nucleotide variantNM_006330.4(LYPLA1):c.472G>A (p.Gly158Ser)not specified [RCV004254959]likely benign85405117954051179Humanname
405816155CV3280984single nucleotide variantNM_006330.4(LYPLA1):c.529G>A (p.Val177Ile)not specified [RCV004411038]uncertain significance85405112254051122Humanname
597645058CV3696917single nucleotide variantNM_006330.4(LYPLA1):c.643A>G (p.Met215Val)not specified [RCV004942318]uncertain significance85404811554048115Humanname
597645065CV3696918single nucleotide variantNM_006330.4(LYPLA1):c.583C>G (p.Pro195Ala)not specified [RCV004942319]uncertain significance85405106854051068Humanname
598163820CV3981420single nucleotide variantNM_006330.4(LYPLA1):c.603A>T (p.Lys201Asn)not specified [RCV005368890]uncertain significance85405104854051048Humanname
598182667CV3981421single nucleotide variantNM_006330.4(LYPLA1):c.380A>T (p.Tyr127Phe)not specified [RCV005372783]uncertain significance85405273754052737Humanname
15134149CV711580single nucleotide variantNM_006330.4(LYPLA1):c.457C>T (p.Pro153Ser)not provided [RCV000965077]benign85405266054052660Humanname