A C to T transition point mutation at nucleotide 886 resulted in a serine to leucine substitution at residue 276 in the Mad homology 2 domain. Phenotypic analysis suggested this allele is hypomorphic. (J:80520)
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A C to T transition point mutation at nucleotide 886 resulted in a serine to leucine substitution at residue 276 in the Mad homology 2 domain. Phenotypic analysis suggested this allele is hypomorphic. (J:80520)