Variant | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Disease | Disease Class | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.851 | 0.280 | MT | 7466 | non coding transcript exon variant | C/-;CC | delins |
|
0.700 | 0 | ||||||||||||
|
0.851 | 0.280 | MT | 7466 | non coding transcript exon variant | C/-;CC | delins |
|
0.700 | 0 | ||||||||||||
|
MT | 7989 | missense variant | T/C | snv |
|
Nutritional and Metabolic Diseases | 0.700 | 0 | |||||||||||||
|
0.851 | 0.200 | MT | 8344 | non coding transcript exon variant | A/G | snv |
|
Nutritional and Metabolic Diseases | 0.700 | 0 | |||||||||||
|
0.851 | 0.200 | MT | 8344 | non coding transcript exon variant | A/G | snv |
|
Nutritional and Metabolic Diseases; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
0.882 | 0.200 | MT | 8356 | non coding transcript exon variant | T/C | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
0.882 | 0.200 | MT | 8356 | non coding transcript exon variant | T/C | snv |
|
0.700 | 0 | ||||||||||||
|
0.882 | 0.200 | MT | 8363 | non coding transcript exon variant | G/A | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
0.882 | 0.200 | MT | 8363 | non coding transcript exon variant | G/A | snv |
|
0.700 | 0 | ||||||||||||
|
1.000 | MT | 8313 | non coding transcript exon variant | G/A | snv |
|
0.700 | 0 | |||||||||||||
|
1.000 | MT | 8342 | non coding transcript exon variant | G/A | snv |
|
0.700 | 0 | |||||||||||||
|
1.000 | MT | 5874 | non coding transcript exon variant | T/C | snv |
|
0.700 | 0 | |||||||||||||
|
1.000 | 0.240 | MT | 5885 | non coding transcript exon variant | T/- | delins |
|
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Eye Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.240 | MT | 5877 | non coding transcript exon variant | C/T | snv |
|
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Eye Diseases; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases | 0.700 | 0 | |||||||||||
|
1.000 | MT | 7526 | non coding transcript exon variant | A/G | snv |
|
0.700 | 0 | |||||||||||||
|
1.000 | MT | 5650 | non coding transcript exon variant | G/A | snv |
|
0.700 | 0 | |||||||||||||
|
1.000 | 0.200 | MT | 5591 | non coding transcript exon variant | G/A | snv |
|
Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.080 | MT | 8087 | frameshift variant | T/- | delins |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.120 | MT | 5667 | non coding transcript exon variant | G/A | snv |
|
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.080 | MT | 5954 | frameshift variant | A/- | del |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases | 0.700 | 0 | |||||||||||
|
MT | 6608 | frameshift variant | C/- | del |
|
0.700 | 0 | ||||||||||||||
|
MT | 6673 | frameshift variant | T/- | delins |
|
0.700 | 0 | ||||||||||||||
|
MT | 6687 | inframe insertion | -/ACC | delins |
|
0.700 | 0 | ||||||||||||||
|
MT | 6692 | frameshift variant | A/- | delins |
|
0.700 | 0 | ||||||||||||||
|
1.000 | MT | 6716 | inframe insertion | -/GGG | delins |
|
0.700 | 0 |