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Variants search result for Homo sapiens
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14 records found for search term Mmp28
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597637465CV3554036single nucleotide variantNM_024302.5(MMP28):c.17G>C (p.Gly6Ala)not specified [RCV004824622]uncertain significance173579536135795361Humanname
156342328CV2343847single nucleotide variantNM_024302.5(MMP28):c.193G>A (p.Ala65Thr)not specified [RCV004193431]uncertain significance173577907435779074Humanname
401746297CV2678810single nucleotide variantNM_024302.5(MMP28):c.194C>T (p.Ala65Val)not specified [RCV004292793]uncertain significance173577907335779073Humanname
405732667CV3322580single nucleotide variantNM_024302.5(MMP28):c.250C>T (p.Arg84Cys)not specified [RCV004464542]uncertain significance173577901735779017Humanname
405731721CV3326298single nucleotide variantNM_024302.5(MMP28):c.103G>C (p.Glu35Gln)not specified [RCV004464422]uncertain significance173579527535795275Humanname
405731954CV3326327single nucleotide variantNM_024302.5(MMP28):c.155A>C (p.Lys52Thr)not specified [RCV004464451]uncertain significance173577928035779280Humanname
407495118CV3457582single nucleotide variantNM_024302.5(MMP28):c.217C>A (p.Pro73Thr)not specified [RCV004643153]uncertain significance173577905035779050Humanname
598200385CV3986045single nucleotide variantNM_024302.5(MMP28):c.205G>C (p.Val69Leu)not specified [RCV005375845]uncertain significance173577906235779062Humanname
598167395CV3986047single nucleotide variantNM_024302.5(MMP28):c.152C>T (p.Pro51Leu)not specified [RCV005369516]uncertain significance173577928335779283Humanname
8636096CV91319single nucleotide variantNM_024302.4(MMP28):c.1419C>T (p.Pro473=)Malignant melanoma [RCV000071417]not provided173576664435766644Humanname
329354016CV2436778single nucleotide variantNM_024302.5(MMP28):c.865G>A (p.Gly289Ser)not specified [RCV004260182]uncertain significance173576836535768365Humanname
598200392CV3986046single nucleotide variantNM_024302.5(MMP28):c.935A>G (p.Gln312Arg)not specified [RCV005375846]uncertain significance173576829535768295Humanname
8636097CV91320single nucleotide variantNM_024302.4(MMP28):c.890G>A (p.Gly297Glu)Malignant melanoma [RCV000071418]not provided173576834035768340Humanname
405715276CV3326260single nucleotide variantNM_024302.5(MMP28):c.1031G>A (p.Gly344Glu)not specified [RCV004462403]uncertain significance173576788935767889Humanname