HelixMTdb (v.20200327) Record for Coding Variant m.14766C>T

Plasmy StatusFrequency
in 195,983
individuals
CountHaplogroup Distribution
Homoplasmic58.525%114700["U",24456],["T",16974],["J",15968],["K",14796],["A",6223],["B",4819],["I",4412],["M",3282],["W",3243],["L3",3090],["C",3075],["X",2786],["L2",2530],["D",2268],["N",1690],["L1",1654],["R",1248],["F",929],["L0",415],["G",299],["E",167],["Y",131],["Z",100],["L4",79],["P",41],["Q",11],["L5",7],["H",5],["L6",1],["S",1]
Heteroplasmic0.017%34["K",5],["L3",4],["T",4],["C",3],["H",3],["J",3],["U",3],["A",2],["I",2],["B",1],["D",1],["L1",1],["W",1],["X + S",1]
Homoplasmic &
Heteroplasmic
Combined
58.543%114734See above