Missense mutation in the DHHC cysteine-rich domain (histidine to alanine).
CA12215632GC
CA?GC
H175A | app-PH; H175A | app-PI; H175A | app-PJ; H175A | app-PK; H175A | app-PL; H175A | app-PM; H175A | app-PO; H175A | app-PR; H175A | app-PT
H?A
A two base substitution (CA to GC) causes a H175A mutation. There is also a silent substitution in the third base of codon P178 (C to A).