RHeference
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7 variants found for this position

VariantRHeference identifierAlleleCategory
exon deletion -> exon deletionRHef00446RHD deletion (RHD*01N.01)exon deletion
exon deletion -> exon deletionRHef00505RHD*Ex1del (RHD*01N.67)exon deletion
single nucleotide polyphormism -> missenseRHef00196RHD*1G,1136T (DAU15)missense
intronic mutation -> silentRHef00560RHD*-115Csilent
intronic mutation -> silentRHef00612RHD*-10C>Tsilent
exon deletion -> exon deletionRHef00773RHD*Ex1-5delexon deletion
exon deletion -> exon deletionRHef00800RHD*Ex1-3delexon deletion