11 variants found for this position
| Variant | RHeference identifier | Allele | Category |
|---|---|---|---|
| single nucleotide polyphormism -> missense | RHef00561 | RHD*CE(1-2)-D[361del11] | missense |
| single nucleotide polyphormism -> missense | RHef00667 | RHD*ce48C(1-2)-DIIIa(3)-ceS(4-7)-D | missense |
| single nucleotide polyphormism -> missense | RHef00015 | RHD*48C,1136T (DAU13) | missense |
| single nucleotide polyphormism -> missense | RHef00770 | RHD*48C,697A,1136T (DAU) | missense |
| single nucleotide polyphormism -> missense | RHef00092 | RHD*48C (DUC3) | missense |
| single nucleotide polyphormism -> missense | RHef00315 | RHD*48C,602G,667G,819A (weak D type 4.1, DAR4) | missense |
| single nucleotide polyphormism -> nonsense | RHef00453 | RHD*48A (W16*, RHD*01N.08) | nonsense |
| single nucleotide polyphormism -> missense | RHef00679 | RHD*48C,520A,1193T | missense |
| single nucleotide polyphormism -> missense | RHef00648 | RHCE*ce48C,697G,733G (ceCF, ce.20.06) | missense |
| single nucleotide polyphormism -> missense | RHef00749 | RHCE*ce48C,365T (ceSL.01 (48C,+/-105G,365T)) | missense |
| single nucleotide polyphormism -> missense | RHef00790 | RHCE*48C,462T,733G,1006T | missense |