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Variants search result for Homo sapiens
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23 records found for search term Mrpl32
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597633784CV3561143single nucleotide variantNM_031903.3(MRPL32):c.5C>T (p.Ala2Val)not specified [RCV004830859]uncertain significance74293239142932391Humanname
401724713CV2714942single nucleotide variantNM_031903.3(MRPL32):c.53G>A (p.Gly18Glu)not specified [RCV004322267]uncertain significance74293243942932439Humanname
401861832CV2766412single nucleotide variantNM_031903.3(MRPL32):c.41C>T (p.Ser14Phe)not specified [RCV004345257]uncertain significance74293242742932427Humanname
405785995CV3371049single nucleotide variantNM_031903.3(MRPL32):c.68A>G (p.Tyr23Cys)not specified [RCV004504820]likely benign74293245442932454Humanname
405786015CV3371053single nucleotide variantNM_031903.3(MRPL32):c.74A>G (p.Glu25Gly)not specified [RCV004504824]uncertain significance74293246042932460Humanname
407525190CV3450340single nucleotide variantNM_031903.3(MRPL32):c.44C>G (p.Ala15Gly)not specified [RCV004631649]uncertain significance74293243042932430Humanname
156253707CV2232546single nucleotide variantNM_031903.3(MRPL32):c.271C>T (p.Arg91Trp)not specified [RCV004099144]uncertain significance74293509542935095Humanname
156353384CV2327526single nucleotide variantNM_031903.3(MRPL32):c.122C>T (p.Pro41Leu)not specified [RCV004176832]uncertain significance74293250842932508Humanname
156194071CV2350686single nucleotide variantNM_031903.3(MRPL32):c.187A>C (p.Ser63Arg)not specified [RCV004207035]uncertain significance74293501142935011Humanname
156345165CV2372879single nucleotide variantNM_031903.3(MRPL32):c.151G>A (p.Gly51Ser)not specified [RCV004223927]uncertain significance74293497542934975Humanname
405785827CV3374574single nucleotide variantNM_031903.3(MRPL32):c.209G>T (p.Ser70Ile)not specified [RCV004504787]uncertain significance74293503342935033Humanname
407474514CV3450338single nucleotide variantNM_031903.3(MRPL32):c.254G>A (p.Arg85His)not specified [RCV004638173]uncertain significance74293507842935078Humanname
407474518CV3450339single nucleotide variantNM_031903.3(MRPL32):c.275G>A (p.Cys92Tyr)not specified [RCV004638174]uncertain significance74293509942935099Humanname
597633777CV3561142single nucleotide variantNM_031903.3(MRPL32):c.160A>G (p.Met54Val)not specified [RCV004830858]uncertain significance74293498442934984Humanname
597637911CV3561145single nucleotide variantNM_031903.3(MRPL32):c.143C>T (p.Ala48Val)not specified [RCV004824823]uncertain significance74293496742934967Humanname
598178873CV3982875single nucleotide variantNM_031903.3(MRPL32):c.274T>C (p.Cys92Arg)not specified [RCV005371838]uncertain significance74293509842935098Humanname
156151631CV2197957single nucleotide variantNM_031903.3(MRPL32):c.494C>T (p.Pro165Leu)not specified [RCV004077170]uncertain significance74293750342937503Humanname
156265245CV2275383single nucleotide variantNM_031903.3(MRPL32):c.328T>C (p.Cys110Arg)not specified [RCV004135265]uncertain significance74293733742937337Humanname
156156911CV2322527single nucleotide variantNM_031903.3(MRPL32):c.377G>A (p.Cys126Tyr)not specified [RCV004182688]uncertain significance74293738642937386Humanname
405785940CV3371039single nucleotide variantNM_031903.3(MRPL32):c.461T>C (p.Ile154Thr)not specified [RCV004504810]uncertain significance74293747042937470Humanname
407474521CV3450341single nucleotide variantNM_031903.3(MRPL32):c.443C>A (p.Pro148His)not specified [RCV004638175]uncertain significance74293745242937452Humanname
407525193CV3450342single nucleotide variantNM_031903.3(MRPL32):c.470T>C (p.Val157Ala)not specified [RCV004631650]uncertain significance74293747942937479Humanname
597633790CV3561144single nucleotide variantNM_031903.3(MRPL32):c.530G>A (p.Arg177Gln)not specified [RCV004830860]uncertain significance74293753942937539Humanname