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 | 0.040 | 11 | 1291476 | intron variant | C/G | snv | 0.12 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||
|
2 | 0.925 | 0.040 | 20 | 63693248 | missense variant | G/A;T | snv | 2.8E-05; 4.0E-06 | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||
|
1 | 1.000 | 0.040 | 4 | 89655739 | intron variant | T/C | snv | 0.37 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||
|
1 | 0.925 | 0.040 | 11 | 1304599 | intron variant | T/C | snv | 9.7E-02 | 0.830 | 1.000 | 1 | 2013 | 2019 | ||||
|
1 | 1.000 | 0.040 | 11 | 1303542 | intron variant | T/A;C | snv | 0.800 | 1.000 | 1 | 2013 | 2013 | |||||
|
1 | 1.000 | 0.040 | 15 | 85756967 | upstream gene variant | G/A | snv | 0.17 | 0.710 | 1.000 | 1 | 2017 | 2017 | ||||
|
1 | 1.000 | 0.040 | 19 | 54420809 | splice region variant | C/G;T | snv | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||
|
1 | 1.000 | 0.040 | 20 | 63688001 | missense variant | G/A;C | snv | 1.6E-05 | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||
|
2 | 0.925 | 0.040 | 20 | 63690162 | inframe deletion | ATGTCATCC/- | delins | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||
|
1 | 1.000 | 0.040 | 20 | 63688161 | missense variant | T/G | snv | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||
|
1 | 1.000 | 0.040 | 20 | 63678184 | splice donor variant | -/T | delins | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||
|
2 | 0.925 | 0.040 | 5 | 1294549 | frameshift variant | -/G | delins | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.040 | 5 | 1255333 | frameshift variant | GA/- | delins | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.040 | 5 | 1293837 | frameshift variant | AG/- | delins | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.040 | 5 | 1294810 | stop gained | C/G;T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.040 | 20 | 63661935 | frameshift variant | TC/- | delins | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.040 | 20 | 63695387 | stop gained | C/G;T | snv | 1.0E-05 | 7.0E-06 | 0.700 | 0 | ||||||
|
1 | 0.827 | 0.080 | 10 | 79557264 | missense variant | C/A | snv | 0.800 | 1.000 | 1 | 2009 | 2009 | |||||
|
1 | 0.827 | 0.080 | 10 | 79557363 | missense variant | A/G | snv | 0.800 | 1.000 | 1 | 2009 | 2009 | |||||
|
4 | 0.882 | 0.080 | 6 | 7562999 | intron variant | T/G | snv | 0.46 | 0.730 | 1.000 | 1 | 2016 | 2019 | ||||
|
4 | 0.882 | 0.160 | 17 | 45847931 | intron variant | C/T | snv | 0.18 | 0.800 | 1.000 | 1 | 2013 | 2013 | ||||
|
4 | 0.851 | 0.160 | 20 | 63695619 | missense variant | G/A | snv | 1.6E-04 | 7.7E-05 | 0.700 | 1.000 | 1 | 2015 | 2015 | |||
|
4 | 0.851 | 0.160 | 20 | 63693211 | stop gained | C/A;G;T | snv | 4.0E-06; 3.2E-05 | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||
|
3 | 0.882 | 0.160 | 20 | 63690442 | splice donor variant | G/A;C | snv | 4.5E-06 | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||
|
2 | 0.925 | 0.160 | 20 | 63687936 | splice acceptor variant | G/A | snv | 0.700 | 1.000 | 1 | 2015 | 2015 |