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 | 0.925 | 0.120 | 20 | 10645245 | frameshift variant | ACTG/- | delins | 0.700 | 1.000 | 4 | 1997 | 2005 | |||||
|
1 | 3 | 114227412 | intron variant | T/C | snv | 9.9E-02 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
6 | 0.882 | 0.120 | 12 | 114385521 | missense variant | C/G;T | snv | 0.010 | 1.000 | 1 | 1999 | 1999 | |||||
|
4 | 0.925 | 0.120 | 12 | 114385522 | missense variant | G/A | snv | 0.010 | 1.000 | 1 | 1999 | 1999 | |||||
|
5 | 0.925 | 0.120 | 12 | 114401830 | missense variant | C/T | snv | 0.010 | 1.000 | 1 | 1999 | 1999 | |||||
|
8 | 0.827 | 0.080 | 8 | 11750213 | missense variant | G/A;C;T | snv | 0.010 | 1.000 | 1 | 2012 | 2012 | |||||
|
3 | 1.000 | 0.080 | 8 | 11755064 | missense variant | A/G;T | snv | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||
|
306 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 0.030 | 1.000 | 3 | 2009 | 2017 | |||||
|
614 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 0.100 | 1.000 | 13 | 2001 | 2019 | |||
|
6 | 0.851 | 0.120 | 1 | 118360355 | intergenic variant | A/G | snv | 0.25 | 0.800 | 1.000 | 1 | 2013 | 2013 | ||||
|
4 | 0.925 | 0.120 | 12 | 119876131 | frameshift variant | AAAGGATTCC/- | delins | 0.700 | 0 | ||||||||
|
1 | 9 | 125915818 | missense variant | C/T | snv | 7.2E-03 | 6.1E-03 | 0.010 | 1.000 | 1 | 2012 | 2012 | |||||
|
6 | 0.851 | 0.120 | 4 | 139874173 | intron variant | G/A | snv | 0.30 | 0.800 | 1.000 | 1 | 2013 | 2013 | ||||
|
1 | 2 | 141204588 | intron variant | G/T | snv | 0.12 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
4 | 0.925 | 8 | 143818378 | missense variant | G/A | snv | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||||
|
7 | 0.851 | 0.240 | 6 | 149378954 | stop gained | C/T | snv | 0.010 | 1.000 | 1 | 2018 | 2018 | |||||
|
246 | 0.430 | 0.880 | 7 | 150999023 | missense variant | T/A;G | snv | 0.75 | 0.010 | 1.000 | 1 | 2008 | 2008 | ||||
|
10 | 0.827 | 0.160 | 1 | 156134830 | missense variant | A/C | snv | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||
|
11 | 0.763 | 0.320 | 1 | 156136984 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 0.010 | 1.000 | 1 | 2004 | 2004 | |||
|
3 | 1.000 | 5 | 160413521 | missense variant | G/A | snv | 1.6E-05 | 3.5E-05 | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||
|
1 | 12 | 16349610 | intron variant | A/G;T | snv | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1 | 10 | 17138170 | 3 prime UTR variant | A/C | snv | 0.51 | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||||
|
1 | 5 | 173233142 | frameshift variant | CCG/AT | delins | 0.700 | 1.000 | 2 | 1998 | 1999 | |||||||
|
1 | 5 | 173233212 | splice region variant | G/C | snv | 0.700 | 0 | ||||||||||
|
2 | 1.000 | 0.080 | 4 | 175023930 | downstream gene variant | T/C | snv | 0.14 | 0.700 | 1.000 | 1 | 2017 | 2017 |