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TYPICAL MUTATIONS

    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

1
Example DYS 449 = 29,    DYS 448 = 19,   DYS 437 = 14
   Generation 2 - sons
2a
449 = 29
2b
449 = 30
    Generation 3 - grandsons
3aa
449 = 29
3ab
449 = 29
3ba
449 = 30
3bb
449 = 30
    Generation 4 - great grandsons
4aaa
448 = 19
4aab
448 = 19
4aba
448 = 18
4abb
448 = 19
4baa
448 = 19
4bab
448 = 19
4bba
448 = 19
4bbb
448 = 19
    Generation 5 - great great grandsons
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).