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Pathways
Variants search result for All species
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8 records found for search term Il3ra
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15188577CV743508single nucleotide variantNM_002183.4(IL3RA):c.408C>T (p.Tyr136=)not provided [RCV000909406]benignX13522091352209Humanname
15188577CV743508single nucleotide variantNM_002183.4(IL3RA):c.408C>T (p.Tyr136=)not provided [RCV000909406]benignY13522091352209Humanname
15171434CV743509single nucleotide variantNM_002183.4(IL3RA):c.1098G>A (p.Glu366=)not provided [RCV000905468]benignX13824261382426Humanname
15171434CV743509single nucleotide variantNM_002183.4(IL3RA):c.1098G>A (p.Glu366=)not provided [RCV000905468]benignY13824261382426Humanname
15152379CV758687single nucleotide variantNM_002183.4(IL3RA):c.257C>T (p.Ala86Val)not provided [RCV000923860]likely benignX13485041348504Humanname
15152379CV758687single nucleotide variantNM_002183.4(IL3RA):c.257C>T (p.Ala86Val)not provided [RCV000923860]likely benignY13485041348504Humanname
15172452CV706341single nucleotide variantNM_002183.4(IL3RA):c.368G>C (p.Ser123Thr)not provided [RCV000950029]likely benignX13521691352169Humanname
15172452CV706341single nucleotide variantNM_002183.4(IL3RA):c.368G>C (p.Ser123Thr)not provided [RCV000950029]likely benignY13521691352169Humanname