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23 records found for search term Tmem141
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
329402502CV2454726single nucleotide variantNM_032928.4(TMEM141):c.4G>C (p.Val2Leu)not specified [RCV004269963]uncertain significance9136791374136791374Humanname
597752711CV3616838single nucleotide variantNM_032928.4(TMEM141):c.8A>G (p.Asn3Ser)not specified [RCV004867216]uncertain significance9136791378136791378Humanname
401721498CV2683527single nucleotide variantNM_032928.4(TMEM141):c.20C>T (p.Ser7Phe)not specified [RCV004282461]uncertain significance9136791390136791390Humanname
156168916CV2276660single nucleotide variantNM_032928.4(TMEM141):c.55G>C (p.Gly19Arg)not specified [RCV004146465]uncertain significance9136791711136791711Humanname
155935087CV2372602single nucleotide variantNM_032928.4(TMEM141):c.52C>T (p.Pro18Ser)not specified [RCV004219393]uncertain significance9136791422136791422Humanname
329355111CV2449140single nucleotide variantNM_032928.4(TMEM141):c.81G>C (p.Gln27His)not specified [RCV004264199]uncertain significance9136791737136791737Humanname
401883578CV2757998single nucleotide variantNM_032928.4(TMEM141):c.88G>T (p.Ala30Ser)not specified [RCV004339169]uncertain significance9136791744136791744Humanname
405794235CV3335938single nucleotide variantNM_032928.4(TMEM141):c.48G>C (p.Lys16Asn)not specified [RCV004475183]uncertain significance9136791418136791418Humanname
407453297CV3486387single nucleotide variantNM_032928.4(TMEM141):c.34G>A (p.Ala12Thr)not specified [RCV004684487]uncertain significance9136791404136791404Humanname
156147876CV2196989single nucleotide variantNM_032928.4(TMEM141):c.236C>T (p.Thr79Met)not specified [RCV004071444]uncertain significance9136792281136792281Humanname
155920818CV2211972single nucleotide variantNM_032928.4(TMEM141):c.286G>A (p.Gly96Arg)not specified [RCV004087098]uncertain significance9136792331136792331Humanname
156129739CV2358727single nucleotide variantNM_032928.4(TMEM141):c.133G>T (p.Ala45Ser)not specified [RCV004209642]uncertain significance9136791958136791958Humanname
405794222CV3335934single nucleotide variantNM_032928.4(TMEM141):c.119C>T (p.Thr40Ile)not specified [RCV004475179]uncertain significance9136791775136791775Humanname
405794706CV3335935single nucleotide variantNM_032928.4(TMEM141):c.211G>C (p.Gly71Arg)not specified [RCV004475180]uncertain significance9136792256136792256Humanname
407453293CV3486386single nucleotide variantNM_032928.4(TMEM141):c.132G>T (p.Met44Ile)not specified [RCV004684486]uncertain significance9136791957136791957Humanname
597752708CV3616837single nucleotide variantNM_032928.4(TMEM141):c.236C>G (p.Thr79Arg)not specified [RCV004867215]uncertain significance9136792281136792281Humanname
598212990CV3917383single nucleotide variantNM_032928.4(TMEM141):c.191T>A (p.Leu64His)not specified [RCV005292233]uncertain significance9136792016136792016Humanname
598212996CV3917384single nucleotide variantNM_032928.4(TMEM141):c.175C>T (p.Pro59Ser)not specified [RCV005292234]uncertain significance9136792000136792000Humanname
598213002CV3917385single nucleotide variantNM_032928.4(TMEM141):c.168T>G (p.Phe56Leu)not specified [RCV005292235]uncertain significance9136791993136791993Humanname
405794230CV3335936single nucleotide variantNM_032928.4(TMEM141):c.302A>T (p.Asp101Val)not specified [RCV004475181]uncertain significance9136792347136792347Humanname
405794233CV3335937single nucleotide variantNM_032928.4(TMEM141):c.321A>T (p.Arg107Ser)not specified [RCV004475182]uncertain significance9136792826136792826Humanname
407453300CV3486388single nucleotide variantNM_032928.4(TMEM141):c.310A>G (p.Thr104Ala)not specified [RCV004684488]uncertain significance9136792355136792355Humanname
598212985CV3917382single nucleotide variantNM_032928.4(TMEM141):c.316C>G (p.Gln106Glu)not specified [RCV005292232]uncertain significance9136792821136792821Humanname