10 variants found for this position
| Variant | RHeference identifier | Allele | Category |
|---|---|---|---|
| single nucleotide polyphormism -> missense | RHef00569 | RHD*D-cE(3-7)-D(weak D Type 2) | missense |
| single nucleotide polyphormism -> missense | RHef00288 | RHD*1154C (weak D type 2) | missense |
| single nucleotide polyphormism -> missense | RHef00289 | RHD*301A,1154C (weak D type 2.1) | missense |
| single nucleotide polyphormism -> missense | RHef00290 | RHD*916A,932G,1154C (weak D type 2.2) | missense |
| single nucleotide polyphormism -> missense | RHef00168 | RHD*1154A (RHD*01N.53) | missense |
| single nucleotide polyphormism -> missense | RHef00406 | RHD*1154T | missense |
| intronic mutation -> silent | RHef00531 | RHD*1154-8A (IVS8-8A, DEL20) | silent |
| intronic mutation -> silent | RHef00542 | RHD*1154-31T (IVS8-31T, DEL37) | silent |
| intronic mutation -> silent | RHef00632 | RHD*1154-1C (IVS8-1C) | silent |
| single nucleotide polyphormism -> missense | RHef00798 | RHD*1154C,1163G | missense |