Sharpin^cpdm-Dem

This allele comprises a C-to-A transition at coding nucleotide 15 near the 5' end of exon 1 (a silent mutation that doesn't change the alanine codon at position 5), followed by a 14 bp deletion of coding nucleotides 19-32. The deletion disrupts the reading frame resulting in a premature stop codon. (J:121810)