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Workpaper for Mitochondrial full sequence analysis



Findings to date

Mitochondrial full sequence analysis identifies the earliest known ancestors genetically related to my mother-line by --

1. Name (six with email addresses)
2. Year Living (one in 1877 in Mexico and two others in 1909 and 1990)
3. Geographical Location (four in the Philippines and the one in Mexico)
4. Closeness of their genetic relationship (one, closest in the Philippines and two less close in Mexico)

Discussion

Mitochondrial full sequence analysis (MFSA) reveals specifics about the geographic origin and world migrations of my mother-line ancestors and others with whom I have a matching relationship. MFSA traces the geographic mitochondrial origin of my mother-line ancestors and that of other testers that match my specific mutation as shown in Figure 15.

the depiction of mtDNA-Ancestral Origins. This is the total number of people with mitochondrial DNA (mtDNA) results from the country of origin in the Family Tree DNA database. It is other testers matching my mother-line. As I am related to these testers by haplogroup mutations genealogically, we share a common ancestor in my direct matrilineal line.

The mtDNA – Ancestral Origins page allows you to view the ancestry information for your matches from one of our mitochondrial DNA (mtDNA) tests.

Country Tab is the maternal country of origin. I show one country of origin for testers who match me, the Philippines.

Match Total is the total number of other testers who match me for a specific country. There are 4.

One of my matches is Genetic Distance 2 from the Philippines and 2 others are Genetic Distancd 2 from Mexico

Figure 15


My matrilineal migrations

My mitochrondrial DNA mutations are shown in Figures 15 and 16 by regions. They have to do with mutation differences. These come about about when a descendant has a genetic trait that her ancestor (mother) did not have. This new trait, referred to as a mutation provides the definitive migration path of my matrilineal ancestors. These mutation differences are shown with mtDNA testing and divided into regions for genealogy purposes.

The Regions

HVR1 – Hypervariable Region 1 – locations 16021-16569 (548 total locations)

HVR2 – Hypervariable Region 2 – locations 1-437 (437 locations)

Coding Region – the balance of the mitochondria (15,445 locations)

The two HVR regions (in red) cover the fewest regions. The Coding Region shown in Figure 16 covers all the regions, including the HVR.

Figure 16
My mtDNA Regions
from Family Tree DNA


The specific mutation results in all the regions of my mitochondria are shown in Figure 17

Figure 17
My mtDNA mutations
from Family Tree DNA


As Figure 17 reports my results from full sequence analysis of my entire mitochondria, all 16,569 locations. This gives me a reliable match with other testers and provides a full haplogroup to look much farther back in time than autosomal and on one specific line.

There are two ways to view these results as shown by the two tabs at the top of the page for – rCRS and RSRS. They are abbreviations for “revised Cambridge Reference Sequence” and “Reconstructed Sapiens Reference Sequence.” The RSRS is a more recent way and the best way to track the mutations backwards in time for comparisons to the Mitochondrial Eve, which simply means as far back as mtDNA could be traced and as human begining.

The alpha-numeric values are the locations in my mitochondrial DNA where a mutation has occurred. The first letter represents the letter that normally found to be present in the "Reference Sequence" and the last letter represents the letter found instead in my mitochondria. This represents a mutation, meaning the genetic trait the descendant's ancestor (mother) didn't have. An example of a mutation for me appears in the Region to the right for the value T9098C. It can be traced in the phylogenetic tree of global human mitochondrial DNA variation. While a study by Soares et al estimates the average mutation rate to be about 1 mutation in 3600 years, most of the 16,569 locations never change. Only the locations that have experienced a mutation are shown. Locations not listed have not experienced a mutation.

Matrilineal matches by person name, year, and location

The report in Figure 18 tells me very specifically about my mother's ancestral line and origins. It also reports other people with mutations matching mine. Ellen Hinkley emphasizes the header tab labed HVR1, HVR2 and coding regions tells me with a high level of certainty whether or not to accept sharing a recent maternal ancestor with someone. It also determines maternal haplogroup with certainty. Note the two names in Figure 18 are fictitious Names and are used for the purpose of illustration.

Figure 18
My mtDNA Genetic Matches
from Family Tree DNA


In mtDNA, to be shown as a match, you must be an exact match in the HVR1 and HVR2 regions, so there is no genetic distance shown, because there are no mutations allowed.

Matching exactly on HVR1 means that you have a 50% chance of sharing a common maternal ancestor within the last fifty-two generations. That is about 1,300 years.

Matching exactly on HVR1 and HVR2 means that you have a 50% chance of sharing a common maternal ancestor within the last twenty-eight generations. That is about 700 years.

However, at the full sequence level shown in the header label (HVR1, HVR2 and Regions), 4 or fewer mismatches are allowed to be considered a match.

The Genetic Distanceshown in Figure 18 means how many mismatches I have in my 16,569 DNA mitochondrial locations compared with the other person’s DNA. Generally, the fewer mismatches mean I am more closely related than to someone with more mismatches.

If my genetic distance is zero, it would bring my match into more recent times. In terms of closeness of relationship, it means that at the 50% CI, I have a 50% chance of sharing a common maternal ancestor within the last 5 generations. That is about 125 years. At the 90% CI Confidence Level I have 90% chance within the last 22 generations, which is about 550 years.

As for how long ago am I related to someone who has a genetic distance of 1 or 2, I'm mindful of Roberta Estes words that "there just isn’t any good measure for mitochondrial DNA mutation timing. Mutations don’t happen on any time schedule, unfortunately. I use genetic distance as a gauge for relative relatedness, no pun intended, and I keep in mind that I might actually be more closely related to someone with a slightly further genetic distance than an exact match."

These markers can be viewed in the International Society of Genetic Genealogists (ISOGG), haplogroup O chart of May, 2018 and by the YFull timeline around the year 2,700 years ago as shown in Table 10. https://www.familytreedna.com/public/mt-dna-haplotree/B

However, as for my goal of a haplogroup portrayal of my clans unique to my ancestral path into the second millennium of the common era. Thus far my research about my maternal clan reveals it can be traced back to the Asian mainland 43,000 years ago with mother-line ancestry in the Philippines before emenating to Mexico at a time yet to be determined.

Useful Links

The Mitrochondrial Haplogroup Tree for haplogroup B.

Using the mtDBA tree.

A good video on the mtDNA Full Sequence panel from FTDNA by Elise Friedman.

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