This graphic is a hypothetical representing the male descendants of 1 man over 4 generations and theY chromosome mutations possible. The letters a and b represent the first and second son respectively.
Blue colour shows those sons with no mutations from the common ancestor.
Brown
colour shows those sons with a mutation increase of 1 at one marker only,
say to 30 at marker 449, commencing at the second son in generation
2
Orange
colour shows those with a mutation decrease of 1 at one marker only, say
to 18 at marker 448.
Red
colour shows a decrease of 2 in a single step mutation at one marker only,
say to 12 at marker 437.
Common Ancestor
|
Example DYS 449 = 29, DYS 448 = 19, DYS 437 = 14 |
|
449 = 29 |
449 = 30 |
|
449 = 29 |
449 = 29 |
449 = 30 |
449 = 30 |
|
448 = 19 |
448 = 19 |
448 = 18 |
448 = 19 |
448 = 19 |
448 = 19 |
448 = 19 |
448 = 19 |
| 5aaaa
437=12 |
5aaab
437=14 |
5aaba
437=14 |
5aabb
437=14 |
5abaa
437=14 |
5abab
437=14 |
5abba
437=14 |
5abbb
437=14 |
5baaa
437=14 |
5baab
437=14 |
5baba
437=14 |
5babb
437=14 |
5bbaa
437=14 |
5bbab
437=14 |
5bbba
437=14 |
5bbbb
437=14 |
With all other markers matched we have 3 x 23/25 matches
| Testees | DYS437 | DYS448 | DYS449 |
| 5aaaa | 12 | 19 | 29 |
| 5abaa | 14 | 18 | 29 |
| 5baaa | 14 | 19 | 30 |
Note that mutations occur randomly at any one marker once in about 500 generations (say 10,000 to 15,000 years), and so, in 25 marker tests, are encountered once in about 20 generations or say 500 years. A single step mutation of 2 would be even rarer. Mutations may be negative (deletions) or positive (insertions).