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Variants search result for Homo sapiens
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12 records found for search term Cd302
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
155907514CV2302231single nucleotide variantNM_014880.5(CD302):c.17T>G (p.Leu6Arg)not specified [RCV004159222]uncertain significance2159798182159798182Humanname
155964259CV2308366single nucleotide variantNM_014880.5(CD302):c.20C>G (p.Pro7Arg)not specified [RCV004164845]uncertain significance2159798179159798179Humanname
329359028CV2425474single nucleotide variantNM_014880.5(CD302):c.13G>A (p.Ala5Thr)not specified [RCV004251127]uncertain significance2159798186159798186Humanname
598207266CV3950732single nucleotide variantNM_014880.5(CD302):c.26T>G (p.Leu9Arg)not specified [RCV005315262]uncertain significance2159798173159798173Humanname
597778619CV3648368single nucleotide variantNM_014880.5(CD302):c.34C>T (p.Pro12Ser)not specified [RCV004898995]uncertain significance2159798165159798165Humanname
401740995CV2690340single nucleotide variantNM_001198759.1(LY75-CD302):c.6G>C (p.Arg2Ser)not specified [RCV004302336]uncertain significance2159904677159904677Humanname
401751515CV2708671single nucleotide variantNM_001198759.1(LY75-CD302):c.275T>G (p.Val92Gly)not specified [RCV004307650]uncertain significance2159898879159898879Humanname
407481099CV3449328single nucleotide variantNM_001198759.1(LY75-CD302):c.619G>A (p.Gly207Ser)not specified [RCV004640312]uncertain significance2159893932159893932Humanname
401884099CV2762697single nucleotide variantNM_001198759.1(LY75-CD302):c.2869C>T (p.Pro957Ser)not specified [RCV004340257]uncertain significance2159852215159852215Humanname
597645670CV3699916single nucleotide variantNM_001198759.1(LY75-CD302):c.1925C>T (p.Pro642Leu)not specified [RCV004942269]uncertain significance2159875493159875493Humanname
407481093CV3449327single nucleotide variantNM_001198759.1(LY75-CD302):c.5518T>C (p.Ser1840Pro)not specified [RCV004640311]uncertain significance2159771955159771955Humanname
8625168CV80287single nucleotide variantNM_001198759.1(LY75-CD302):c.5023G>A (p.Asp1675Asn)Malignant melanoma [RCV000060363]not provided2159783437159783437Humanname