6 variants found for this position
| Variant | RHeference identifier | Allele | Category |
|---|---|---|---|
| intronic mutation -> silent | RHef00565 | RHD*1227A,149-29C (IVS1-29C) | silent |
| exon deletion -> exon deletion | RHef00650 | RHD*Ex2del | exon deletion |
| single nucleotide polyphormism -> missense | RHef00229 | RHD*149A | missense |
| intronic mutation -> silent | RHef00539 | RHD*149-29C (IVS1-29C, DEL32) | silent |
| intronic mutation -> silent | RHef00632 | RHD*1154-1C (IVS8-1C) | silent |
| intronic mutation -> silent | RHef00598 | M1 | silent |