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Variants search result for Homo sapiens
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6 records found for search term Ypel5
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401897299CV2789997single nucleotide variantNM_016061.3(YPEL5):c.77A>G (p.Asn26Ser)not specified [RCV004363957]uncertain significance23015672830156728Humanname
407456468CV3493860single nucleotide variantNM_016061.3(YPEL5):c.65C>T (p.Thr22Met)not specified [RCV004685986]uncertain significance23015671630156716Humanname
156264523CV2329445single nucleotide variantNM_016061.3(YPEL5):c.175C>G (p.Arg59Gly)not specified [RCV004187450]uncertain significance23015865230158652Humanname
156203671CV2335005single nucleotide variantNM_016061.3(YPEL5):c.230A>G (p.Asn77Ser)not specified [RCV004182096]uncertain significance23015870730158707Humanname
329397816CV2464041single nucleotide variantNM_016061.3(YPEL5):c.263C>T (p.Thr88Ile)not specified [RCV004273747]uncertain significance23015874030158740Humanname
8630312CV85467single nucleotide variantNM_001127399.1(YPEL5):c.47C>T (p.Ser16Phe)Malignant melanoma [RCV000065550]not provided23015669830156698Humanname