9 variants found for this position
| Variant | RHeference identifier | Allele | Category |
|---|---|---|---|
| intronic mutation -> silent | RHef00506 | RHD*634+1T,1136T (DAU, RHD*01N.69) | silent |
| single nucleotide polyphormism -> missense | RHef00294 | RHD*634T (weak D type 23) | missense |
| single nucleotide polyphormism -> missense | RHef00255 | RHD*634A (weak D type 111) | missense |
| single nucleotide polyphormism -> missense | RHef00159 | RHD*634C (DEL16) | missense |
| intronic mutation -> silent | RHef00528 | RHD*634+5T (IVS4+5T, DEL14) | silent |
| intronic mutation -> silent | RHef00529 | RHD*634+5A (IVS4+5A) | silent |
| intronic mutation -> silent | RHef00710 | RHD*336-3T (IVS4+1A) | silent |
| intronic mutation -> silent | RHef00711 | RHD*634+2A (IVS4+2A) | silent |
| intronic mutation -> silent | RHef00563 | RHD*634+1T (IVS4+1T) | silent |