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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.925 | 0.120 | 2 | 27444430 | 3 prime UTR variant | A/G;T | snv | 0.42 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases | 0.700 | 1.000 | 2 | 2010 | 2013 | |||||||
|
0.925 | 0.120 | 2 | 27444430 | 3 prime UTR variant | A/G;T | snv | 0.42 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases | 0.700 | 1.000 | 2 | 2010 | 2013 | |||||||
|
0.925 | 0.120 | 2 | 27458731 | intron variant | A/C;G;T | snv | 0.42; 4.1E-06 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases | 0.700 | 1.000 | 2 | 2010 | 2013 | |||||||
|
0.925 | 0.120 | 2 | 27458731 | intron variant | A/C;G;T | snv | 0.42; 4.1E-06 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases | 0.700 | 1.000 | 2 | 2010 | 2013 | |||||||
|
0.925 | 0.120 | 2 | 27461867 | intron variant | A/G;T | snv | 0.42; 4.0E-06 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases | 0.700 | 1.000 | 2 | 2010 | 2013 | |||||||
|
0.925 | 0.120 | 2 | 27461867 | intron variant | A/G;T | snv | 0.42; 4.0E-06 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases | 0.700 | 1.000 | 2 | 2010 | 2013 | |||||||
|
0.925 | 0.120 | 2 | 27480628 | intron variant | A/G;T | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.925 | 0.120 | 2 | 27480628 | intron variant | A/G;T | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.925 | 2 | 27447567 | missense variant | A/G | snv |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||||
|
1.000 | 2 | 27477310 | missense variant | A/T | snv |
|
0.800 | 1.000 | 1 | 2013 | 2013 | ||||||||||
|
0.925 | 2 | 27480124 | stop gained | G/A | snv | 4.0E-06 |
|
0.700 | 0 | ||||||||||||
|
0.925 | 2 | 27480124 | stop gained | G/A | snv | 4.0E-06 |
|
0.700 | 0 | ||||||||||||
|
1.000 | 2 | 27485431 | stop gained | G/A;C | snv | 2.4E-05; 8.0E-06 |
|
0.700 | 0 | ||||||||||||
|
1.000 | 2 | 27471096 | splice acceptor variant | C/A;T | snv | 4.2E-06; 8.4E-06 |
|
0.700 | 0 | ||||||||||||
|
0.925 | 2 | 27447567 | missense variant | A/G | snv |
|
0.700 | 0 | |||||||||||||
|
1.000 | 2 | 27457638 | splice donor variant | C/T | snv |
|
0.700 | 0 | |||||||||||||
|
1.000 | 2 | 27470948 | frameshift variant | TC/-;TCTC | delins |
|
0.700 | 0 | |||||||||||||
|
1.000 | 2 | 27476657 | inframe deletion | TCAATA/- | delins |
|
0.700 | 0 | |||||||||||||
|
1.000 | 2 | 27453428 | stop gained | G/A | snv | 8.0E-06 |
|
0.700 | 0 | ||||||||||||
|
0.882 | 0.080 | 2 | 27459399 | stop gained | -/T | delins | 1.2E-05 |
|
0.700 | 0 | |||||||||||
|
0.882 | 0.080 | 2 | 27459399 | stop gained | -/T | delins | 1.2E-05 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | 0.700 | 0 | ||||||||||
|
0.882 | 0.080 | 2 | 27459399 | stop gained | -/T | delins | 1.2E-05 |
|
0.700 | 0 | |||||||||||
|
1.000 | 2 | 27446314 | missense variant | G/T | snv |
|
0.800 | 0 | |||||||||||||
|
1.000 | 2 | 27445929 | missense variant | A/C | snv |
|
0.800 | 0 | |||||||||||||
|
1.000 | 2 | 27481061 | missense variant | A/G | snv |
|
0.800 | 0 |