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Variant Information

Gene Interpretation
WT1 chr11:32417914 chr11:32396368 c.1136_1137insGACTCTTGTA p.R380Tfs*8 Pathogenic
WT1 chr11:32417910 chr11:32396364 c.1142C>A p.Ser381Ter Pathogenic
WT1 chr11:32417907 chr11:32396361 c.1143_1144insTCGG p.A382Sfs*4 Pathogenic
WT1 chr11:32413560 chr11:32392014 c.1390G>A p.D464N Pathogenic