3 variants found for this position
| Variant | RHeference identifier | Allele | Category |
|---|---|---|---|
| single nucleotide polyphormism -> missense | RHef00243 | RHD*1177C,1199C (weak D type 10.2) | missense |
| single nucleotide polyphormism -> missense | RHef00367 | RHD*1199C (weak D type 81) | missense |
| single nucleotide polyphormism -> missense | RHef00271 | RHD*1199T (weak D type 126) | missense |