Amino acid replacement: C601Y.
Missense mutation in furin-like repeat (extracellular domain IV).
G21556750A
G34331A
C601Y | Egfr-PA; C650Y | Egfr-PB
C601Y
EgfrS2145 mutant embryos show cardioblast (CB) patterning defects and a lower generic CBs:ostial CBs ratio than the typical 4:2 ratio.