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Variants search result for Homo sapiens
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20 records found for search term Nmt1
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597654322CV3566311single nucleotide variantNM_021079.5(NMT1):c.7G>C (p.Asp3His)not specified [RCV004827246]uncertain significance174506133645061336Humanname
8636197CV91421single nucleotide variantNM_021079.4(NMT1):c.16G>A (p.Glu6Lys)Malignant melanoma [RCV000071519]not provided174506134545061345Humanname
156152568CV2265924single nucleotide variantNM_021079.5(NMT1):c.218C>T (p.Ser73Leu)not specified [RCV004126771]uncertain significance174508173045081730Humanname
329367966CV2442597single nucleotide variantNM_021079.5(NMT1):c.229C>A (p.Gln77Lys)not specified [RCV004264956]uncertain significance174508174145081741Humanname
401738019CV2700903single nucleotide variantNM_021079.5(NMT1):c.143C>T (p.Pro48Leu)not specified [RCV004307169]uncertain significance174508165545081655Humanname
597654345CV3566314single nucleotide variantNM_021079.5(NMT1):c.112G>A (p.Asp38Asn)not specified [RCV004827249]uncertain significance174506144145061441Humanname
156361167CV2269184single nucleotide variantNM_021079.5(NMT1):c.871G>A (p.Val291Ile)not specified [RCV004130345]uncertain significance174509853945098539Humanname
156184391CV2377718single nucleotide variantNM_021079.5(NMT1):c.605G>A (p.Arg202Gln)not specified [RCV004230308]uncertain significance174509713645097136Humanname
329356273CV2442560single nucleotide variantNM_021079.5(NMT1):c.995C>G (p.Thr332Ser)not specified [RCV004266782]uncertain significance174510295245102952Humanname
401878902CV2773771single nucleotide variantNM_021079.5(NMT1):c.316G>T (p.Ala106Ser)not specified [RCV004356437]uncertain significance174508658345086583Humanname
597654335CV3566313single nucleotide variantNM_021079.5(NMT1):c.682G>A (p.Ala228Thr)not specified [RCV004827248]uncertain significance174509721345097213Humanname
598206274CV4004387single nucleotide variantNM_021079.5(NMT1):c.502G>A (p.Val168Met)not specified [RCV005376890]uncertain significance174509380145093801Humanname
156328804CV2213685single nucleotide variantNM_021079.5(NMT1):c.1088C>T (p.Thr363Met)not specified [RCV004089761]uncertain significance174510304545103045Humanname
156157538CV2359969single nucleotide variantNM_021079.5(NMT1):c.1093G>A (p.Val365Ile)not specified [RCV004212812]uncertain significance174510305045103050Humanname
156347278CV2382871single nucleotide variantNM_021079.5(NMT1):c.1405A>G (p.Ile469Val)not specified [RCV004217472]uncertain significance174510493145104931Humanname
329382778CV2424551single nucleotide variantNM_021079.5(NMT1):c.1205C>T (p.Thr402Met)not specified [RCV004254052]uncertain significance174510374945103749Humanname
401771655CV2686283single nucleotide variantNM_021079.5(NMT1):c.1006G>A (p.Ala336Thr)not specified [RCV004297367]uncertain significance174510296345102963Humanname
405725424CV3359225single nucleotide variantNM_021079.5(NMT1):c.1061C>G (p.Thr354Ser)not specified [RCV004495729]uncertain significance174510301845103018Humanname
407497880CV3458898single nucleotide variantNM_021079.5(NMT1):c.1303A>T (p.Met435Leu)not specified [RCV004643862]uncertain significance174510384745103847Humanname
597654328CV3566312single nucleotide variantNM_021079.5(NMT1):c.1304T>C (p.Met435Thr)not specified [RCV004827247]uncertain significance174510384845103848Humanname