chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
MT
13822
13823
C
T
771
GENIC
possibly homozygous
109049494
MT
13879
13880
C
A
755
GENIC
possibly homozygous
109024987
MT
13974
13975
G
A
877
GENIC
homozygous
109024989
