RHeference
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17 variants found for this position

VariantRHeference identifierAlleleCategory
single nucleotide polyphormism -> missenseRHef00445RHD*CE(1-9)-D (RHD*01N.02)missense
single nucleotide polyphormism -> missenseRHef00449RHD*D[203G>C]-Ce(3-9)-Dmissense
single nucleotide polyphormism -> missenseRHef00112RHD*CE(1-3)-D (RHD*01N.43)missense
single nucleotide polyphormism -> missenseRHef00114RHD*D-CE(2-5)-Dmissense
single nucleotide polyphormism -> missenseRHef00124RHD*D-CE(2)-D(1063A)missense
single nucleotide polyphormism -> missenseRHef00561RHD*CE(1-2)-D[361del11]missense
single nucleotide polyphormism -> missenseRHef00667RHD*ce48C(1-2)-DIIIa(3)-ceS(4-7)-Dmissense
single nucleotide polyphormism -> missenseRHef00421RHD*D-ceAG(2)-Dmissense
single nucleotide polyphormism -> missenseRHef00016RHD*201A,203A,1136T (DAU14)missense
single nucleotide polyphormism -> missenseRHef00060RHD*D-ce(2)-DIIIa (DIII type 7)missense
single nucleotide polyphormism -> missenseRHef00115RHD*150C,178C,201A,203A,307C (DIIIb Caucasian)missense
single nucleotide polyphormism -> missenseRHef00074RHD*D-CE(2-3)-D (DKK, RHD*45)missense
single nucleotide polyphormism -> missenseRHef00005RHD*150C,178C,201A,203A,602G,667G,957A,1025C (DAR6, DAR(ce2))missense
single nucleotide polyphormism -> missenseRHef00300RHD*178C,201A,203A,594T,667G,744T,957A,1025C (weak D type 29)missense
single nucleotide polyphormism -> missenseRHef00177RHD*178C,201A,203A,594T,667G,744T,941T,1025Cmissense
single nucleotide polyphormism -> missenseRHef00359RHD*203C (weak D type 74)missense
single nucleotide polyphormism -> missenseRHef00514RHD*150C,178C,201A,203A,307C,702delG (RHD*01N.83)missense