3 variants found for this position

VariantRHeference identifierAlleleCategory
single nucleotide polyphormism -> missenseRHef00043RHD*505C,509G,514T,539C (DFR3, RHD*17.03)missense
single nucleotide polyphormism -> missenseRHef00366RHD*539A (weak D type 80)missense
deletion-insertion -> missenseRHef00810RHD*539_540delinsTTmissense