CCDC162P, coiled-coil domain containing 162, pseudogene, 221262
N. diseases: 21; N. variants: 176
Source: ALL
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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1.000 | 0.080 | 6 | 109322402 | intron variant | -/T | delins |
|
Respiratory Tract Diseases; Nervous System Diseases | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
6 | 109261139 | intron variant | A/-;AA | delins |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||||
|
6 | 109261139 | intron variant | A/-;AA | delins |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||||
|
6 | 109287257 | intron variant | A/C | snv | 0.51 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
6 | 109292049 | intron variant | A/C;T | snv |
|
0.800 | 1.000 | 2 | 2009 | 2017 | |||||||||||
|
6 | 109292049 | intron variant | A/C;T | snv |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||||
|
6 | 109292049 | intron variant | A/C;T | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||||
|
6 | 109311596 | intron variant | A/G | snv | 0.40 |
|
0.800 | 1.000 | 2 | 2009 | 2017 | ||||||||||
|
6 | 109311596 | intron variant | A/G | snv | 0.40 |
|
0.700 | 1.000 | 2 | 2017 | 2018 | ||||||||||
|
6 | 109301291 | intron variant | A/G | snv | 0.30 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
6 | 109319285 | intron variant | A/G | snv | 0.29 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
6 | 109240832 | intron variant | A/G | snv | 0.48 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
6 | 109313625 | intron variant | A/G | snv | 0.26 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | ||||||||||
|
6 | 109313625 | intron variant | A/G | snv | 0.26 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | ||||||||||
|
6 | 109313625 | intron variant | A/G | snv | 0.26 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | ||||||||||
|
6 | 109313625 | intron variant | A/G | snv | 0.26 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | ||||||||||
|
6 | 109327150 | intron variant | A/G | snv | 0.25 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
6 | 109328452 | intron variant | A/G | snv | 0.25 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
6 | 109232561 | intron variant | A/G | snv | 0.25 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
6 | 109231231 | intron variant | A/G | snv | 0.24 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
6 | 109229944 | intron variant | A/G | snv | 0.25 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
6 | 109227634 | non coding transcript exon variant | A/G | snv | 0.28 | 0.25 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
6 | 109182773 | intron variant | A/G | snv | 0.59 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
6 | 109216350 | intron variant | A/G | snv | 0.47 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
6 | 109203214 | intron variant | A/G | snv | 0.23 |
|
0.700 | 1.000 | 1 | 2012 | 2012 |