AFG3L1P, AFG3 like matrix AAA peptidase subunit 1, pseudogene, 172
N. diseases: 5; N. variants: 11
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 | 0.040 | 16 | 89984281 | intron variant | G/T | snv | 0.60 |
|
Neoplasms | 0.700 | 1.000 | 2 | 2011 | 2012 | |||||||
|
0.925 | 0.120 | 16 | 90000528 | non coding transcript exon variant | A/C;T | snv |
|
Neoplasms | 0.800 | 1.000 | 2 | 2009 | 2017 | ||||||||
|
16 | 89995916 | non coding transcript exon variant | CT/- | delins | 0.14 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 0.040 | 16 | 90001533 | non coding transcript exon variant | G/A | snv | 0.49 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2011 | 2011 | |||||||
|
1.000 | 0.040 | 16 | 89979578 | non coding transcript exon variant | A/G | snv | 0.17 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2011 | 2011 | |||||||
|
16 | 89973042 | intron variant | G/C | snv | 0.64 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
16 | 89996071 | non coding transcript exon variant | G/A;C | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
1.000 | 0.040 | 16 | 89984281 | intron variant | G/T | snv | 0.60 |
|
0.700 | 1.000 | 1 | 2008 | 2008 | ||||||||
|
1.000 | 0.040 | 16 | 89977620 | non coding transcript exon variant | C/G;T | snv | 0.40 |
|
0.700 | 1.000 | 1 | 2008 | 2008 | ||||||||
|
1.000 | 0.040 | 16 | 89977620 | non coding transcript exon variant | C/G;T | snv | 0.40 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2011 | 2011 | |||||||
|
1.000 | 0.040 | 16 | 89984472 | intron variant | A/C;G | snv |
|
Neoplasms | 0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.925 | 0.120 | 16 | 90000528 | non coding transcript exon variant | A/C;T | snv |
|
0.700 | 1.000 | 1 | 2008 | 2008 | |||||||||
|
0.925 | 0.120 | 16 | 90000528 | non coding transcript exon variant | A/C;T | snv |
|
Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases | 0.700 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
16 | 89986579 | intron variant | G/A | snv | 1.1E-02 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
16 | 89988301 | intron variant | T/C;G | snv |
|
0.700 | 1.000 | 1 | 2015 | 2015 |