3 variants found for this position

Variant	RHeference identifier	Allele	Category
deletion -> frameshift	RHef00484	RHD1228-2del21 (F410fs, RHD*01N.44)	frameshift
single nucleotide polyphormism -> missense	RHef00363	RHD*1228G (weak D type 78)	missense
intronic mutation -> silent	RHef00511	RHD1228-1A (IVS9-1A, RHD01N.77)	silent