Table 1.
Patient | AFR | EUR | NAM | Mutation | Mutations' reference |
---|---|---|---|---|---|
01 | 24.6 | 16.7 | 58.7 | c.1473T>A:p.Cys491∗ | [18] |
02 | 7.6 | 43.5 | 48.9 | c.2672del:p.Asp891Alafs∗15 | [18] |
03 | 21.6 | 14.8 | 63.6 | c.2672del:p.Asp891Alafs∗15 | [18] |
04 | 16 | 42.2 | 41.8 | c.2672del:p.Asp891Alafs∗15 | [18] |
05 | 9.1 | 8.9 | 82 | c.1486T>C:p.Trp496Arg | [18] |
06 | 22.5 | 39.6 | 37.9 | [c.757G>A:p.Gly253Arg; c.1352G>T:p.Gly451Val] | [18] |
07 | 7.2 | 55.3 | 37.5 | [c.757G>A:p.Gly253Arg; c.1352G>T:p.Gly451Val] | [18] |
08 | 28.2 | 31.9 | 39.9 | [c.757G>A:p.Gly253Arg; c.1352G>T:p.Gly451Val] | [18] |
09 | 5 | 58.7 | 36.3 | [c.757G>A:p.Gly253Arg; c.1352G>T:p.Gly451Val] | [18] |
10 | 11.9 | 37.2 | 50.9 | [c.757G>A:p.Gly253Arg; c.1352G>T:p.Gly451Val] | [18] |
11 | 9.3 | 32.1 | 58.6 | [c.757G>A:p.Gly253Arg; c.1352G>T:p.Gly451Val] | [18] |
12 | 11 | 25.7 | 63.3 | [c.757G>A:p.Gly253Arg; c.1352G>T:p.Gly451Val] | [18] |
AFR: African ancestry; EUR: European ancestry; NAM: Native American ancestry.