4 variants found for this position
| Variant | RHeference identifier | Allele | Category |
|---|---|---|---|
| intronic mutation -> exon deletion | RHef00570 | RHD*Ex3del,602G,667G,819A | exon deletion |
| single nucleotide polyphormism -> missense | RHef00215 | RHD*335T (01N.68) | missense |
| single nucleotide polyphormism -> missense | RHef00216 | RHD*335C (DEL42) | missense |
| intronic mutation -> silent | RHef00467 | RHD*335+1A (IVS2+1A, RHD*01N.24) | silent |