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16 records found for search term Ndufa7
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156276842CV2328099single nucleotide variantNM_005001.5(NDUFA7):c.5C>T (p.Ala2Val)not specified [RCV004173215]uncertain significance1983213548321354Humanname
597683255CV3559020single nucleotide variantNM_005001.5(NDUFA7):c.8C>T (p.Ser3Phe)not specified [RCV004829527]uncertain significance1983213518321351Humanname
405814638CV3341629single nucleotide variantNM_005001.5(NDUFA7):c.22A>G (p.Ile8Val)not specified [RCV004484515]uncertain significance1983213378321337Humanname
597669193CV3559023single nucleotide variantNM_005001.5(NDUFA7):c.90G>C (p.Glu30Asp)not specified [RCV004829529]uncertain significance1983208688320868Humanname
156100282CV2306609single nucleotide variantNM_005001.5(NDUFA7):c.172G>A (p.Asp58Asn)not specified [RCV004157210]uncertain significance1983165758316575Humanname
405814629CV3341624single nucleotide variantNM_005001.5(NDUFA7):c.215C>T (p.Ser72Leu)not specified [RCV004484510]uncertain significance1983165328316532Humanname
405814647CV3341634single nucleotide variantNM_005001.5(NDUFA7):c.281C>T (p.Ala94Val)not specified [RCV004484520]uncertain significance1983115668311566Humanname
597669166CV3559018single nucleotide variantNM_005001.5(NDUFA7):c.158A>G (p.Tyr53Cys)not specified [RCV004829525]uncertain significance1983165898316589Humanname
597669174CV3559019single nucleotide variantNM_005001.5(NDUFA7):c.190G>A (p.Val64Met)not specified [RCV004829526]uncertain significance1983165578316557Humanname
598230731CV4004054single nucleotide variantNM_005001.5(NDUFA7):c.179G>A (p.Arg60His)not specified [RCV005381241]uncertain significance1983165688316568Humanname
598230743CV4004056single nucleotide variantNM_005001.5(NDUFA7):c.125C>A (p.Pro42His)not specified [RCV005381243]uncertain significance1983166228316622Humanname
598230752CV4004057single nucleotide variantNM_005001.5(NDUFA7):c.176G>A (p.Gly59Asp)not specified [RCV005381244]uncertain significance1983165718316571Humanname
598230758CV4004058single nucleotide variantNM_005001.5(NDUFA7):c.119A>G (p.Lys40Arg)not specified [RCV005381245]uncertain significance1983166288316628Humanname
155989813CV2285173single nucleotide variantNM_005001.5(NDUFA7):c.326A>C (p.Asp109Ala)not specified [RCV004145385]uncertain significance1983115218311521Humanname
597669184CV3559021single nucleotide variantNM_005001.5(NDUFA7):c.307A>G (p.Arg103Gly)not specified [RCV004829528]uncertain significance1983115408311540Humanname
598230737CV4004055single nucleotide variantNM_005001.5(NDUFA7):c.323C>T (p.Ser108Leu)not specified [RCV005381242]uncertain significance1983115248311524Humanname