Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs3761548
rs3761548
0.620 0.680 X 49261784 intron variant G/A;T snv
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.020 1.000 2 2014 2018
dbSNP: rs55958994
rs55958994
0.925 0.080 12 52907235 intron variant C/T snv 0.12
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 1.000 1 2019 2019
dbSNP: rs104893626
rs104893626
0.827 0.280 2 136114915 stop gained G/C snv
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 1.000 1 2014 2014
dbSNP: rs438034
rs438034
0.882 0.120 1 214657274 stop gained A/G;T snv 0.61
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 1.000 1 2011 2011
dbSNP: rs562015640
rs562015640
0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 < 0.001 1 2018 2018
dbSNP: rs113488022
rs113488022
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.100 0.857 14 2010 2019
dbSNP: rs121913377
rs121913377
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.100 0.857 14 2010 2019
dbSNP: rs121913529
rs121913529
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.050 0.800 5 2011 2017
dbSNP: rs121434569
rs121434569
0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.040 1.000 4 2016 2019
dbSNP: rs351855
rs351855
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.030 1.000 3 2004 2015
dbSNP: rs1284806277
rs1284806277
MOK
0.827 0.200 14 102251978 missense variant A/G snv 1.4E-05
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.020 1.000 2 2011 2016
dbSNP: rs2273535
rs2273535
0.645 0.360 20 56386485 missense variant A/C;T snv 0.28
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.020 1.000 2 2018 2018
dbSNP: rs752021744
rs752021744
0.689 0.440 3 138759306 missense variant T/C snv 1.2E-05
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.020 1.000 2 2011 2012
dbSNP: rs762846821
rs762846821
0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.020 1.000 2 2012 2013
dbSNP: rs10009228
rs10009228
4 40354405 missense variant A/G snv 0.78 0.76
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 1.000 1 2012 2012
dbSNP: rs1042028
rs1042028
0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 1.000 1 2019 2019
dbSNP: rs104894230
rs104894230
0.564 0.600 11 534288 missense variant C/A;G;T snv
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 1.000 1 2011 2011
dbSNP: rs1057519710
rs1057519710
KIT
0.695 0.280 4 54733166 missense variant G/C;T snv
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 1.000 1 2005 2005
dbSNP: rs1057519771
rs1057519771
1.000 0.080 9 130872201 missense variant G/C snv
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 1.000 1 2019 2019
dbSNP: rs1057519847
rs1057519847
0.570 0.560 7 55191821 missense variant CT/AG mnv
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 1.000 1 2012 2012
dbSNP: rs1057519848
rs1057519848
0.570 0.560 7 55191822 missense variant TG/GT mnv
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 1.000 1 2012 2012
dbSNP: rs11549465
rs11549465
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 1.000 1 2014 2014
dbSNP: rs11549467
rs11549467
0.653 0.400 14 61740857 missense variant G/A snv 8.9E-03 7.0E-03
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 1.000 1 2014 2014
dbSNP: rs121434568
rs121434568
0.568 0.560 7 55191822 missense variant T/A;G snv
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 1.000 1 2012 2012
dbSNP: rs121913279
rs121913279
0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 1.000 1 2016 2016