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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
3 | 1.000 | 0.040 | 11 | 2167905 | missense variant | C/T | snv | 1.1E-04 | 1.4E-04 | 0.700 | 1.000 | 7 | 1998 | 2015 | |||
|
2 | 1.000 | 0.200 | 2 | 72888457 | missense variant | A/G | snv | 5.6E-05 | 5.6E-05 | 0.700 | 1.000 | 5 | 2001 | 2013 | |||
|
2 | 1.000 | 0.080 | 9 | 129814062 | inframe deletion | CTC/- | delins | 4.9E-05 | 0.700 | 1.000 | 2 | 1997 | 1998 | ||||
|
3 | 1.000 | 0.040 | 14 | 54844023 | missense variant | C/G | snv | 4.0E-06 | 0.010 | 1.000 | 1 | 1999 | 1999 | ||||
|
3 | 1.000 | 19 | 35720980 | stop gained | C/T | snv | 0.010 | 1.000 | 1 | 2016 | 2016 | ||||||
|
3 | 1.000 | 19 | 35721775 | stop gained | C/T | snv | 0.010 | 1.000 | 1 | 2016 | 2016 | ||||||
|
3 | 1.000 | 0.040 | 2 | 178436264 | missense variant | G/A | snv | 9.9E-05 | 9.1E-05 | 0.010 | 1.000 | 1 | 2015 | 2015 | |||
|
2 | 1.000 | 0.200 | 2 | 72891502 | stop gained | A/T | snv | 8.0E-05 | 5.6E-05 | 0.700 | 1.000 | 1 | 2006 | 2006 | |||
|
4 | 1.000 | 2 | 218649090 | frameshift variant | TT/- | del | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
4 | 1.000 | 2 | 218646330 | frameshift variant | C/- | del | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
5 | 1.000 | 0.160 | 8 | 60266044 | missense variant | A/C;G | snv | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||
|
4 | 1.000 | 0.080 | 5 | 141955844 | stop gained | C/A | snv | 4.0E-06 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
3 | 1.000 | 0.080 | 1 | 32893848 | missense variant | G/A | snv | 4.9E-04 | 7.0E-05 | 0.010 | 1.000 | 1 | 2017 | 2017 | |||
|
4 | 1.000 | 0.040 | 21 | 25975997 | missense variant | T/C | snv | 4.0E-06 | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||
|
3 | 1.000 | 0.080 | 1 | 32889110 | missense variant | C/A;T | snv | 4.0E-06 | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||
|
3 | 1.000 | 0.080 | 1 | 32889123 | missense variant | C/A | snv | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||
|
4 | 1.000 | 0.080 | 3 | 123319754 | missense variant | C/T | snv | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||
|
2 | 1.000 | 0.080 | MT | 14597 | missense variant | A/G | snv | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||
|
4 | 1.000 | 0.080 | 3 | 123291354 | missense variant | A/T | snv | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||
|
2 | 1.000 | 0.160 | 18 | 23544424 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
3 | 1.000 | 8 | 23007711 | missense variant | G/A | snv | 0.700 | 0 | |||||||||
|
6 | 1.000 | 0.080 | 5 | 111482938 | splice donor variant | G/A | snv | 0.700 | 0 | ||||||||
|
4 | 1.000 | 0.120 | 14 | 54844138 | missense variant | A/G | snv | 0.700 | 0 | ||||||||
|
2 | 1.000 | 0.080 | X | 41524036 | splice acceptor variant | T/A;C | snv | 0.700 | 0 | ||||||||
|
2 | 1.000 | 0.040 | 11 | 2164339 | missense variant | G/A | snv | 4.0E-05 | 2.1E-05 | 0.700 | 0 |