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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1 | 1.000 | 0.080 | 5 | 37049240 | missense variant | G/A | snv | 0.800 | 1.000 | 12 | 2004 | 2017 | |||||
|
1 | 1.000 | 0.080 | 5 | 37049239 | missense variant | C/G;T | snv | 0.800 | 1.000 | 12 | 2004 | 2017 | |||||
|
1 | 1.000 | 0.080 | 5 | 37052471 | missense variant | G/A | snv | 0.800 | 1.000 | 10 | 2004 | 2017 | |||||
|
1 | 1.000 | 0.080 | 5 | 37057211 | missense variant | A/G | snv | 0.800 | 1.000 | 9 | 2004 | 2017 | |||||
|
1 | 1.000 | 0.080 | 5 | 37002734 | missense variant | C/G | snv | 0.800 | 1.000 | 9 | 2004 | 2017 | |||||
|
1 | 1.000 | 0.080 | 5 | 36962199 | missense variant | G/A | snv | 3.8E-03 | 3.6E-03 | 0.700 | 1.000 | 9 | 2004 | 2017 | |||
|
5 | 0.882 | 0.120 | 5 | 37044480 | missense variant | G/C;T | snv | 0.800 | 1.000 | 9 | 2004 | 2017 | |||||
|
1 | 1.000 | 0.080 | 5 | 37049282 | missense variant | G/T | snv | 0.800 | 1.000 | 9 | 2004 | 2017 | |||||
|
1 | 1.000 | 0.080 | 5 | 36971002 | missense variant | A/G | snv | 0.800 | 1.000 | 9 | 2004 | 2017 | |||||
|
1 | 1.000 | 0.080 | 5 | 36955467 | splice region variant | A/C;G | snv | 0.700 | 1.000 | 3 | 2004 | 2007 | |||||
|
1 | 1.000 | 0.080 | 5 | 36995805 | splice donor variant | G/A | snv | 0.700 | 1.000 | 2 | 2010 | 2013 | |||||
|
1 | 1.000 | 0.080 | 5 | 37057336 | splice region variant | A/G | snv | 0.700 | 1.000 | 2 | 2004 | 2007 | |||||
|
1 | 1.000 | 0.080 | 5 | 37022036 | intron variant | A/G | snv | 0.700 | 1.000 | 2 | 2016 | 2016 | |||||
|
1 | 1.000 | 0.080 | 5 | 37048558 | missense variant | T/C | snv | 0.700 | 1.000 | 2 | 2014 | 2014 | |||||
|
5 | 0.925 | 0.120 | 5 | 37052453 | stop gained | C/T | snv | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||
|
1 | 1.000 | 0.080 | 5 | 36962121 | splice acceptor variant | A/G | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||
|
1 | 1.000 | 0.080 | 5 | 37017071 | missense variant | T/C | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||
|
1 | 1.000 | 0.080 | 5 | 37020458 | splice acceptor variant | G/C | snv | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||
|
1 | 1.000 | 0.080 | 5 | 37046137 | missense variant | T/C | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||
|
1 | 1.000 | 0.080 | 5 | 37003348 | splice donor variant | G/A;T | snv | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||
|
1 | 1.000 | 0.080 | 5 | 36971037 | splice donor variant | G/A | snv | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||
|
1 | 1.000 | 0.080 | 5 | 36955540 | stop gained | C/T | snv | 0.700 | 1.000 | 1 | 2010 | 2010 | |||||
|
1 | 1.000 | 0.080 | 5 | 37052478 | missense variant | G/A | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||
|
1 | 1.000 | 0.080 | 5 | 36953698 | start lost | T/A | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.080 | 5 | 37020615 | stop gained | C/T | snv | 0.700 | 0 |