4 variants found for this position
Variant | RHeference identifier | Allele | Category |
---|---|---|---|
single nucleotide polyphormism -> missense | RHef00352 | RHD*165T,1213G (weak D type 68) | missense |
single nucleotide polyphormism -> nonsense | RHef00498 | RHD*1213T (Q405*, RHD*01N.60) | nonsense |
single nucleotide polyphormism -> missense | RHef00767 | RHD*1213A | missense |
single nucleotide polyphormism -> missense | RHef00821 | RHD*1213G | missense |