rs121913036
|
|
1.000 |
|
22 |
50526638 |
missense variant
|
T/G
|
snv
|
5.3E-05
|
4.9E-05
|
Mitochondrial DNA Depletion Syndrome 1
|
0.700 |
1.000 |
5 |
1999 |
2013 |
rs1064792870
|
|
1.000 |
|
22 |
50527170 |
missense variant
|
T/G
|
snv
|
|
7.0E-06
|
Mitochondrial DNA Depletion Syndrome 1
|
0.700 |
1.000 |
1 |
2004 |
2004 |
rs761665644
|
|
0.925 |
0.120 |
22 |
50527606 |
missense variant
|
T/G
|
snv
|
8.0E-06
|
|
Peripheral Neuropathy
|
0.700 |
|
0 |
|
|
rs761665644
|
|
0.925 |
0.120 |
22 |
50527606 |
missense variant
|
T/G
|
snv
|
8.0E-06
|
|
Mitochondrial DNA Depletion Syndrome 1
|
0.700 |
|
0 |
|
|
rs761665644
|
|
0.925 |
0.120 |
22 |
50527606 |
missense variant
|
T/G
|
snv
|
8.0E-06
|
|
Extraocular Muscle Paresis
|
0.700 |
|
0 |
|
|
rs761665644
|
|
0.925 |
0.120 |
22 |
50527606 |
missense variant
|
T/G
|
snv
|
8.0E-06
|
|
Gastrointestinal dysmotility
|
0.700 |
|
0 |
|
|
rs1064792877
|
|
1.000 |
|
22 |
50526143 |
splice acceptor variant
|
T/C;G
|
snv
|
|
|
Mitochondrial DNA Depletion Syndrome 1
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs149977726
|
|
1.000 |
|
22 |
50527265 |
missense variant
|
T/C
|
snv
|
1.2E-05
|
9.8E-05
|
Mitochondrial DNA Depletion Syndrome 1
|
0.800 |
1.000 |
1 |
1999 |
2002 |
rs1064792871
|
|
1.000 |
|
22 |
50526657 |
missense variant
|
G/C
|
snv
|
|
|
Mitochondrial DNA Depletion Syndrome 1
|
0.700 |
1.000 |
1 |
2004 |
2004 |
rs80358232
|
|
1.000 |
0.200 |
22 |
50523738 |
missense variant
|
G/A;T
|
snv
|
4.0E-06
|
|
Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency
|
0.800 |
|
0 |
|
|
rs11479
|
|
0.925 |
0.080 |
22 |
50525807 |
stop gained
|
G/A;C;T
|
snv
|
0.13;
1.3E-05;
4.3E-06
|
|
Mitochondrial DNA Depletion Syndrome 1
|
0.700 |
1.000 |
1 |
2007 |
2007 |
rs28937598
|
|
1.000 |
0.200 |
22 |
50523901 |
missense variant
|
G/A
|
snv
|
1.2E-05
|
7.0E-06
|
Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency
|
0.800 |
1.000 |
0 |
1999 |
2015 |
rs74315510
|
|
0.925 |
0.240 |
22 |
50524255 |
stop gained
|
G/A
|
snv
|
8.4E-05
|
3.5E-05
|
Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency
|
0.700 |
|
0 |
|
|
rs74315510
|
|
0.925 |
0.240 |
22 |
50524255 |
stop gained
|
G/A
|
snv
|
8.4E-05
|
3.5E-05
|
MYOPIA 6 (disorder)
|
0.700 |
|
0 |
|
|
rs74315512
|
|
1.000 |
0.200 |
22 |
50524144 |
stop gained
|
G/A
|
snv
|
1.6E-05
|
|
Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency
|
0.700 |
|
0 |
|
|
rs1064792887
|
|
1.000 |
|
22 |
50527210 |
frameshift variant
|
G/-
|
delins
|
|
|
Mitochondrial DNA Depletion Syndrome 1
|
0.700 |
1.000 |
1 |
2002 |
2002 |
rs1064792888
|
|
1.000 |
|
22 |
50526720 |
frameshift variant
|
G/-
|
delins
|
|
|
Mitochondrial DNA Depletion Syndrome 1
|
0.700 |
1.000 |
1 |
2005 |
2005 |
rs1064792890
|
|
1.000 |
|
22 |
50525873 |
frameshift variant
|
CTGAGCGCGGGGCCGTCCCG/-
|
delins
|
|
|
Mitochondrial DNA Depletion Syndrome 1
|
0.700 |
1.000 |
1 |
2005 |
2005 |
rs201685922
|
|
1.000 |
|
22 |
50526479 |
splice region variant
|
CGGG/-
|
delins
|
1.4E-02
|
1.3E-02
|
Mitochondrial DNA Depletion Syndrome 1
|
0.700 |
1.000 |
1 |
2000 |
2000 |
rs786205098
|
|
1.000 |
|
22 |
50526103 |
inframe deletion
|
CCAGCG/-
|
delins
|
1.2E-05
|
2.1E-05
|
Mitochondrial DNA Depletion Syndrome 1
|
0.700 |
1.000 |
1 |
1999 |
1999 |
rs1060499534
|
|
1.000 |
|
22 |
50526246 |
missense variant
|
C/T
|
snv
|
7.1E-06
|
|
Mitochondrial DNA Depletion Syndrome 1
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs1064792869
|
|
1.000 |
|
22 |
50527215 |
missense variant
|
C/T
|
snv
|
|
|
Mitochondrial DNA Depletion Syndrome 1
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs1064792872
|
|
1.000 |
|
22 |
50526611 |
missense variant
|
C/T
|
snv
|
|
|
Mitochondrial DNA Depletion Syndrome 1
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs1064792873
|
|
1.000 |
|
22 |
50526141 |
missense variant
|
C/T
|
snv
|
|
|
Mitochondrial DNA Depletion Syndrome 1
|
0.700 |
1.000 |
1 |
2005 |
2005 |
rs1064792874
|
|
1.000 |
|
22 |
50526019 |
missense variant
|
C/T
|
snv
|
|
|
Mitochondrial DNA Depletion Syndrome 1
|
0.700 |
1.000 |
1 |
2004 |
2004 |