Variant | Gene | N. diseases v | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
2 | 0.925 | 0.120 | X | 111410215 | missense variant | C/T | snv | 0.800 | 1.000 | 15 | 1998 | 2016 | |||||
|
3 | 0.882 | 0.120 | X | 111401121 | missense variant | G/A | snv | 0.800 | 1.000 | 15 | 1998 | 2016 | |||||
|
2 | 0.925 | 0.120 | X | 111401322 | missense variant | A/G | snv | 0.800 | 1.000 | 15 | 1998 | 2016 | |||||
|
3 | 0.882 | 0.120 | X | 111401087 | missense variant | G/C;T | snv | 0.800 | 1.000 | 15 | 1998 | 2016 | |||||
|
2 | 0.925 | 0.120 | X | 111410260 | missense variant | T/G | snv | 0.800 | 1.000 | 15 | 1998 | 2016 | |||||
|
3 | 0.882 | 0.120 | X | 111410223 | missense variant | C/A;T | snv | 0.800 | 1.000 | 15 | 1998 | 2016 | |||||
|
2 | 0.925 | 0.080 | X | 111410166 | missense variant | C/A;T | snv | 0.800 | 1.000 | 8 | 1998 | 2002 | |||||
|
2 | 0.925 | 0.080 | X | 111410134 | stop gained | G/A;C | snv | 0.800 | 1.000 | 8 | 1998 | 2002 | |||||
|
2 | 0.925 | 0.120 | X | 111410188 | missense variant | C/A | snv | 0.800 | 1.000 | 7 | 1998 | 2016 | |||||
|
3 | 0.882 | 0.120 | X | 111401108 | missense variant | C/A;T | snv | 9.5E-06 | 0.800 | 1.000 | 7 | 1998 | 2016 | ||||
|
1 | 1.000 | 0.080 | X | 111333074 | missense variant | T/C | snv | 0.700 | 1.000 | 15 | 1998 | 2016 | |||||
|
2 | 0.925 | 0.080 | X | 111410249 | missense variant | C/A | snv | 0.700 | 1.000 | 8 | 1998 | 2002 | |||||
|
2 | 0.925 | 0.080 | X | 111410109 | missense variant | A/C | snv | 0.700 | 1.000 | 8 | 1998 | 2002 | |||||
|
2 | 0.925 | 0.080 | X | 111401163 | missense variant | G/A;C | snv | 0.700 | 1.000 | 8 | 1998 | 2002 | |||||
|
2 | 0.925 | 0.080 | X | 111401162 | missense variant | C/A | snv | 0.700 | 1.000 | 8 | 1998 | 2002 | |||||
|
3 | 0.882 | 0.080 | X | 111401139 | missense variant | G/A | snv | 0.700 | 1.000 | 8 | 1998 | 2002 | |||||
|
2 | 0.925 | 0.080 | X | 111401123 | missense variant | G/C | snv | 0.700 | 1.000 | 8 | 1998 | 2002 | |||||
|
2 | 0.925 | 0.080 | X | 111401088 | missense variant | T/C | snv | 0.700 | 1.000 | 8 | 1998 | 2002 | |||||
|
2 | 0.925 | 0.080 | X | 111401054 | missense variant | A/G | snv | 0.700 | 1.000 | 8 | 1998 | 2002 | |||||
|
2 | 0.925 | 0.080 | X | 111333108 | missense variant | C/A | snv | 0.700 | 1.000 | 8 | 1998 | 2002 | |||||
|
2 | 0.925 | 0.080 | X | 111410271 | missense variant | A/G | snv | 0.700 | 1.000 | 7 | 1998 | 2016 | |||||
|
2 | 0.925 | 0.080 | X | 111410209 | missense variant | A/T | snv | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||
|
1 | 1.000 | 0.080 | X | 111333153 | missense variant | C/T | snv | 9.5E-06 | 0.700 | 0 | |||||||
|
2 | 0.925 | 0.120 | X | 111401010 | frameshift variant | AG/- | delins | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.080 | X | 111401151 | missense variant | C/A | snv | 0.700 | 0 |