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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
MT | 12271 | non coding transcript exon variant | T/C | snv |
|
Nutritional and Metabolic Diseases | 0.700 | 0 | |||||||||||||
|
MT | 12283 | non coding transcript exon variant | G/A | snv |
|
Nutritional and Metabolic Diseases | 0.700 | 0 | |||||||||||||
|
0.925 | 0.200 | MT | 12258 | non coding transcript exon variant | C/A | snv |
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases | 0.700 | 0 | |||||||||||
|
0.925 | 0.200 | MT | 12258 | non coding transcript exon variant | C/A | snv |
|
0.700 | 0 | ||||||||||||
|
1.000 | MT | 12207 | non coding transcript exon variant | G/A | snv |
|
0.700 | 0 | |||||||||||||
|
1.000 | 0.120 | MT | 10438 | non coding transcript exon variant | A/G | snv |
|
Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
0.925 | 0.200 | MT | 12315 | non coding transcript exon variant | G/A | snv |
|
Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
MT | 12320 | non coding transcript exon variant | A/G | snv |
|
Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases | 0.700 | 0 | |||||||||||||
|
1.000 | MT | 12183 | non coding transcript exon variant | G/A | snv |
|
0.700 | 0 | |||||||||||||
|
0.925 | 0.200 | MT | 12147 | non coding transcript exon variant | G/A | snv |
|
0.700 | 0 | ||||||||||||
|
1.000 | 0.080 | MT | 9997 | non coding transcript exon variant | T/C | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases | 0.700 | 0 | |||||||||||
|
MT | 10010 | non coding transcript exon variant | T/C | snv |
|
0.700 | 0 | ||||||||||||||
|
1.000 | 0.120 | MT | 8839 | missense variant | G/A;C | snv |
|
Nutritional and Metabolic Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.080 | MT | 9273 | protein altering variant | -/ATC | ins |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases | 0.700 | 0 | |||||||||||
|
1.000 | MT | 9311 | inframe insertion | -/GCA | ins |
|
0.700 | 0 | |||||||||||||
|
1.000 | 0.080 | MT | 9429 | protein altering variant | -/CCC | ins |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases | 0.700 | 0 | |||||||||||
|
1.000 | MT | 9431 | frameshift variant | -/A | ins |
|
0.700 | 0 | |||||||||||||
|
1.000 | 0.080 | MT | 9441 | inframe insertion | -/TTT | delins |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.160 | MT | 10664 | synonymous variant | C/T | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
0.742 | 0.320 | MT | 8993 | missense variant | T/C;G | snv |
|
Nutritional and Metabolic Diseases | 0.700 | 0 | |||||||||||
|
0.742 | 0.320 | MT | 8993 | missense variant | T/C;G | snv |
|
0.700 | 0 | ||||||||||||
|
0.742 | 0.320 | MT | 8993 | missense variant | T/C;G | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | 0.700 | 0 | |||||||||||
|
0.742 | 0.320 | MT | 8993 | missense variant | T/C;G | snv |
|
0.700 | 0 | ||||||||||||
|
0.742 | 0.320 | MT | 8993 | missense variant | T/C;G | snv |
|
0.700 | 0 | ||||||||||||
|
0.742 | 0.320 | MT | 8993 | missense variant | T/C;G | snv |
|
Female Urogenital Diseases and Pregnancy Complications | 0.700 | 0 |