4 variants found for this position
| Variant | RHeference identifier | Allele | Category |
|---|---|---|---|
| single nucleotide polyphormism -> missense | RHef00662 | RHD*667G,697C,1136T,1177C (DAU) | missense |
| single nucleotide polyphormism -> missense | RHef00241 | RHD*1177C (weak D type 10) | missense |
| single nucleotide polyphormism -> missense | RHef00242 | RHD*1145C,1177C (weak D type 10.1) | missense |
| single nucleotide polyphormism -> missense | RHef00243 | RHD*1177C,1199C (weak D type 10.2) | missense |