Nucleotide substitution: G955A. Amino acid replacement: D319N. Also, deletion of nucleotides 961-975 resulting in deletion of codons 322-326.
This small deletion of amino acid residues 322-326 occurs in conjunction with a point mutation that causes amino acid change D319N.
G8067200A
G955A
D319N | mys-PA; D319N | mys-PB; D319N | mys-PC; D319N | mys-PD
D319N
This point mutation occurs in conjunction with a deletion that removes amino acids 322-326.