Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Disease | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
15 | 99974409 | missense variant | T/C;G | snv | 0.66; 4.0E-06 |
|
0.700 | 1.000 | 2 | 2015 | 2019 | ||||||||||
|
1.000 | 0.080 | 15 | 100152748 | missense variant | G/A;T | snv | 7.1E-02; 3.2E-05 |
|
0.700 | 1.000 | 2 | 2017 | 2019 | ||||||||
|
1.000 | 0.080 | 15 | 100152748 | missense variant | G/A;T | snv | 7.1E-02; 3.2E-05 |
|
0.700 | 1.000 | 2 | 2017 | 2018 | ||||||||
|
15 | 99993107 | missense variant | C/T | snv | 2.0E-04 | 2.0E-04 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
15 | 100132203 | intron variant | A/G | snv | 9.0E-03 | 5.2E-03 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
1.000 | 0.040 | 15 | 100188458 | intron variant | G/A;C | snv |
|
0.800 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
15 | 99972953 | 3 prime UTR variant | C/T | snv | 0.62 |
|
0.700 | 1.000 | 1 | 2014 | 2014 | ||||||||||
|
15 | 99973858 | 3 prime UTR variant | C/T | snv | 0.63 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
15 | 99972912 | 3 prime UTR variant | G/A | snv | 0.61 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
15 | 100314288 | intron variant | C/T | snv | 0.19 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
15 | 100052239 | intron variant | -/AA | ins | 7.0E-06 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
15 | 100254158 | synonymous variant | C/T | snv | 0.75 | 0.76 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
15 | 100255167 | intron variant | G/A;T | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
15 | 100246066 | intron variant | A/G | snv | 0.63 |
|
0.700 | 1.000 | 1 | 2008 | 2008 | ||||||||||
|
15 | 100218180 | intron variant | C/G;T | snv |
|
0.700 | 1.000 | 1 | 2013 | 2013 | |||||||||||
|
15 | 100219409 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2010 | 2010 | |||||||||||
|
15 | 100261237 | intron variant | A/G | snv | 0.72 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
15 | 100260635 | intron variant | A/C | snv | 0.68 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 0.080 | 15 | 100152748 | missense variant | G/A;T | snv | 7.1E-02; 3.2E-05 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 0.080 | 15 | 100152748 | missense variant | G/A;T | snv | 7.1E-02; 3.2E-05 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 0.080 | 15 | 100152748 | missense variant | G/A;T | snv | 7.1E-02; 3.2E-05 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
15 | 100183232 | intron variant | G/T | snv | 3.4E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 |