Figure 8.
This is an explanation using our proposed method for the variant MYO7A NM_000260.4(MYO7A):c.5618G>A (p.Arg1873Gln). The "*" in "p.R1861*" refers to mutation to any amino acid.
This is an explanation using our proposed method for the variant MYO7A NM_000260.4(MYO7A):c.5618G>A (p.Arg1873Gln). The "*" in "p.R1861*" refers to mutation to any amino acid.