18 variants found for this position
| Variant | RHeference identifier | Allele | Category |
|---|---|---|---|
| single nucleotide polyphormism -> missense | RHef00445 | RHD*CE(1-9)-D (RHD*01N.02) | missense |
| single nucleotide polyphormism -> missense | RHef00112 | RHD*CE(1-3)-D (RHD*01N.43) | missense |
| single nucleotide polyphormism -> missense | RHef00114 | RHD*D-CE(2-5)-D | missense |
| single nucleotide polyphormism -> missense | RHef00124 | RHD*D-CE(2)-D(1063A) | missense |
| single nucleotide polyphormism -> missense | RHef00561 | RHD*CE(1-2)-D[361del11] | missense |
| single nucleotide polyphormism -> missense | RHef00667 | RHD*ce48C(1-2)-DIIIa(3)-ceS(4-7)-D | missense |
| single nucleotide polyphormism -> missense | RHef00421 | RHD*D-ceAG(2)-D | missense |
| single nucleotide polyphormism -> missense | RHef00060 | RHD*D-ce(2)-DIIIa (DIII type 7) | missense |
| single nucleotide polyphormism -> missense | RHef00115 | RHD*150C,178C,201A,203A,307C (DIIIb Caucasian) | missense |
| single nucleotide polyphormism -> missense | RHef00074 | RHD*D-CE(2-3)-D (DKK, RHD*45) | missense |
| single nucleotide polyphormism -> missense | RHef00302 | RHD*8G,178C (weak D type 3.1) | missense |
| single nucleotide polyphormism -> missense | RHef00005 | RHD*150C,178C,201A,203A,602G,667G,957A,1025C (DAR6, DAR(ce2)) | missense |
| single nucleotide polyphormism -> missense | RHef00300 | RHD*178C,201A,203A,594T,667G,744T,957A,1025C (weak D type 29) | missense |
| single nucleotide polyphormism -> missense | RHef00177 | RHD*178C,201A,203A,594T,667G,744T,941T,1025C | missense |
| single nucleotide polyphormism -> missense | RHef00415 | RHD*178C | missense |
| single nucleotide polyphormism -> missense | RHef00129 | RHD*178C,689T (RHD*60) | missense |
| single nucleotide polyphormism -> missense | RHef00178 | RHD*178G,307C,482C,640T,966C | missense |
| single nucleotide polyphormism -> missense | RHef00514 | RHD*150C,178C,201A,203A,307C,702delG (RHD*01N.83) | missense |