Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1556424691
CYTB ; ND6 ; TRNT
0.851 0.200 MT 15923 non coding transcript exon variant A/G snv 13
rs199476105
ND5 ; CYTB ; ND6
0.851 0.200 MT 14459 missense variant G/A snv 4
rs28357681
ND6 ; CYTB
0.851 0.040 MT 14798 missense variant T/C snv 4
rs121434453
TRNE ; ND6 ; CYTB
0.882 0.320 MT 14709 non coding transcript exon variant T/C snv 4
rs28359178
CYTB ; ND5 ; ND6
0.882 0.280 MT 13708 missense variant G/A snv 3
rs387906421
CYTB ; TRNE ; ND6
0.925 0.200 MT 14674 non coding transcript exon variant T/C;G snv 3
rs207459997
ND6 ; CYTB
0.925 MT 15615 missense variant G/A snv 3
rs41518645
ND6 ; CYTB
0.925 0.200 MT 15257 missense variant G/A snv 3
rs199476109
ND6 ; CYTB ; ND5
0.882 0.120 MT 14487 missense variant T/C snv 3
rs199474701
TRNP ; ND6 ; CYTB
0.925 0.200 MT 15967 non coding transcript exon variant G/A snv 3
rs1057518882
CYTB ; ND5 ; ND6
MT 14598 missense variant T/C snv 2
rs207459998
CYTB ; ND6
1.000 MT 14846 missense variant G/A snv 2
rs207459999
CYTB ; ND6
0.925 0.160 MT 15242 stop gained G/A snv 2
rs207460000
CYTB ; ND6
1.000 MT 15150 stop gained G/A snv 2
rs207460001
CYTB ; ND6
MT 15197 missense variant T/C snv 2
rs199476107
ND5 ; ND6 ; CYTB
0.925 0.200 MT 14453 missense variant G/A snv 2
rs797045055
ND5 ; ND6 ; CYTB
1.000 0.080 MT 14597 missense variant A/G snv 2
rs199951903
ND6 ; CYTB
0.925 0.120 MT 15497 missense variant G/A snv 2
rs199476104
ND6 ; CYTB ; ND5
0.925 0.160 MT 14484 missense variant T/C snv 2
rs387906424
ND6 ; ND5 ; CYTB
0.925 0.200 MT 14596 missense variant A/T snv 2
rs397515506
CYTB ; ND5 ; ND6
1.000 0.160 MT 14568 missense variant C/T snv 1
rs869312882
CYTB ; ND5 ; ND6
1.000 0.040 MT 14243 frameshift variant -/C delins 1
rs193302985
CYTB ; ND6
1.000 0.080 MT 15043 synonymous variant G/A snv 1
rs193302991
CYTB ; ND6
1.000 0.080 MT 15301 synonymous variant G/A snv 1
rs200336777
CYTB ; ND6
1.000 0.160 MT 15812 missense variant G/A snv 1