BELL DNA PROJECT

Mitochondrial DNA Results

From FTDNA:

"The mitochondrion sequenced in 1981 became known as the Cambridge Reference Sequence (CRS) and has been used as a basis for comparison with your mtDNA. In other words, any place in your mtDNA where you have a difference from the CRS, is characterized as a mutation. If your results show no mutations at all, it means that your mtDNA matches the CRS."

Row Kit Code Haplogroup HVR1 differences HVR2 differences ybase
1
1228
3310
X
16093C, 16223T
263G, 315.1C
2
23217
3330
H
none
73G, 263G, 309.1C, 315.1C, 523-, 524-
3 39717 3341 J*
16069T,16126C,16145A
4 44136 3343 J1b1
16069T,16093C,16126C,16145A,16172C,16222T,16261T
QAEY9
5 52678 3349 W
16037G,16184T,16223T,16292T,16519C
73G,119C,189G,195C,204C,207A,263G,315.1C
6 N16450 3357 H
16304C
309.1C, 309.2C, 315.1C, 456T
7 66043 3358 H
16519C
8 74227 3361 H
16519C
210G, 263G, 309.1C, 309.2C, 315.1C
9 77673 3364 H
16051G, 16162G, 16213A, 16266T, 16519C
73G, 263G, 315.1C
10 83183 3368 U2
16051G,16092C,16129C,16182C,16183C,16189C,16362C,16519C
73G,146C,152C,217C,263G,309.1C,309.2C,315.1C,508G,573.1C,573.2C 
11 N47891 3376 HV*
16298C
72C, 195C, 263G, 309.1C, 315.1C
12 N29299 3379 H5
16304C
263G,309.1C,315.1C,456T,573.1C,573.2C
13 90822 3380 H1
16519C
146C, 152C, 200G, 263G, 309.1C, 315.1C
14 98221 3382 H
16213A, 16519C
15 109538 3385 L2a
16223T,16278T,16294T,16309G,16390A
73G,143A,146C,152C,263G,309.1C,315.1C,522-,523-
16 118247 3395 L2a
16189C,16192T,16223T,16278T,16294T,16309G,16390A
17 N54718 3401 T*
16126C,16294T,16519C
18 134287 3408 HV*
16192T,16311C,16335G
195C,263G,309.1C,315.1C 
19 135281 3409 K
16224C,16311C,16320T,16356C,16519C
73G,146C,152C,263G,315.1C,498-,573.1C 
20 137642 3410 K
16129A,16224C,16311C,16519C
16T,73G,150T,152C,199C,263G,309.1C,315.1C,497T
21 138896 3414 L1b 16126C,16187T,16189C,16223T,16264T,16270T,16278T,16311C,16519C

Updated: 5 January 2009