HelixMTdb (v.20200327) Record for Coding Variant m.16278C>T

Plasmy StatusFrequency
in 195,983
individuals
CountHaplogroup Distribution
Homoplasmic5.783%11334["X",2686],["L2",2506],["L1",1625],["J",954],["H",820],["U",690],["L3",619],["B",201],["T",159],["G",157],["C",121],["L0",116],["M",116],["K",93],["I",88],["W",82],["D",78],["A",62],["R",52],["HV",48],["P",23],["N",12],["V",10],["L5",7],["F",6],["Z",2],["L6",1]
Heteroplasmic0.061%120["H",39],["U",19],["T",10],["X + S",10],["L2",8],["J",5],["L1",5],["HV",4],["V",3],["A",2],["D",2],["K",2],["L3",2],["W",2],["B",1],["E",1],["G",1],["I",1],["M",1],["N",1],["R",1]
Homoplasmic &
Heteroplasmic
Combined
5.844%11454See above