7 variants found for this position
| Variant | RHeference identifier | Allele | Category |
|---|---|---|---|
| intronic mutation -> silent | RHef00541 | RHD*1073+152A,1227A (IVS7+152A, DEL36) | silent |
| intronic mutation -> exon deletion | RHef00537 | RHD*Ex8del (DEL30) | exon deletion |
| single nucleotide polyphormism -> missense | RHef00109 | RHD*1073C (DWI, RHD*33) | missense |
| intronic mutation -> silent | RHef00507 | RHD*1073+1T (IVS7+1T, RHD*01N.70) | silent |
| intronic mutation -> silent | RHef00495 | RHD*1073+2C (IVS7+2C, RHD*01N.56) | silent |
| intronic mutation -> silent | RHef00681 | RHD*1073+1A (IVS7+1A) | silent |
| intronic mutation -> silent | RHef00736 | RHD*1073+2A (IVS7+2A) | silent |