2 variants found for this position

Variant	RHeference identifier	Allele	Category
single nucleotide polyphormism -> missense	RHef00242	RHD*1145C,1177C (weak D type 10.1)	missense
single nucleotide polyphormism -> missense	RHef00379	RHD*1145C (weak D type 92)	missense