Insertions are types of DNA mutations. They are places in your DNA where nucleotides (Cytosine, Guanine, Adenine, and Thymine) have been added to the DNA sequence.
In in the example below, the sequence has an insertion at position 309. An insertion is denoted by a .1. The nucleotide added is Cytosine, therefore denoted with a C. The insertion then looks like this: 309.1C.
Haplogroup – H |
HVR1 differences from RSRS |
A16129G |
T16187C |
C16189T |
T16223C |
G16230A |
T16278C |
C16311T |
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HVR2 differences from RSRS |
G73A |
C146T |
C152T |
C195T |
A247G |
309.1C |
315.1C |
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Coding Region differences from RSRS |
A769G |
A825t |
A1018G |
G2706A |
A2758G |
C2885T |
T3594C |
G4104A |
T4312C |
T7028C |
G7146A |
T7256C |
A7521G |
T8468C |
T8655C |
G8701A |
C9540T |
G10398A |
T10664C |
A10688G |
C10810T |
C10873T |
C10915T |
A11719G |
A11914G |
T12705C |
G13105A |
G13276A |
T13506C |
T13650C |
T14766C |
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A site may have consecutive insertions.
If you have a two-nucleotide insertion, we show the result like this: 309.1C, 309.2C. It indicates that two extra copies of Cytosine have been inserted at position 309.
Haplogroup – H |
HVR1 differences from RSRS |
A16129G |
T16187C |
C16189T |
T16223C |
G16230A |
T16278C |
C16311T |
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HVR2 differences from RSRS |
G73A |
C146T |
C152T |
C195T |
A247G |
309.1C |
309.2C |
315.1C |
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Coding Region differences from RSRS |
A769G |
A825t |
A1018G |
G2706A |
A2758G |
C2885T |
T3594C |
G4104A |
T4312C |
T7028C |
G7146A |
T7256C |
A7521G |
T8468C |
T8655C |
G8701A |
C9540T |
G10398A |
T10664C |
A10688G |
C10810T |
C10873T |
C10915T |
A11719G |
A11914G |
T12705C |
G13105A |
G13276A |
T13506C |
T13650C |
T14766C |
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