HelixMTdb (v.20200327) Record for Coding Variant m.489T>C

Plasmy StatusFrequency
in 195,983
individuals
CountHaplogroup Distribution
Homoplasmic12.980%25439["J",15938],["M",3303],["C",3062],["D",2266],["E",334],["G",298],["Z",101],["U",70],["H",13],["K",12],["Q",11],["L3",7],["A",6],["HV",4],["V",4],["F",2],["L2",2],["I",1],["L1",1],["N",1],["R",1],["T",1],["W",1]
Heteroplasmic0.031%60["J",28],["C",13],["M",5],["D",3],["H",3],["I",2],["T",2],["U",2],["A",1],["W",1]
Homoplasmic &
Heteroplasmic
Combined
13.011%25499See above