4 variants found for this position
| Variant | RHeference identifier | Allele | Category |
|---|---|---|---|
| single nucleotide polyphormism -> missense | RHef00256 | RHD*635A (weak D type 112) | missense |
| single nucleotide polyphormism -> missense | RHef00160 | RHD*635T (RHD*01N.15) | missense |
| intronic mutation -> silent | RHef00443 | RHD*635-2C (IVS4-2C, RHD*54) | silent |
| intronic mutation -> silent | RHef00530 | RHD*635-2G (IVS4-2G, DEL19) | silent |