Source: ALL

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: rs1163944538
rs1163944538
0.641 0.560 17 75494905 frameshift variant -/A delins 4.0E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 0
dbSNP: rs1352010373
rs1352010373
0.641 0.560 17 75489265 splice acceptor variant G/C snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 0
dbSNP: rs1565400045
rs1565400045
ATM
11 108259050 frameshift variant A/- del
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 0
dbSNP: rs1565486028
rs1565486028
ATM
11 108307917 frameshift variant -/G delins
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 0
dbSNP: rs1567489890
rs1567489890
1.000 0.120 16 2077476 non coding transcript exon variant G/A snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 0
dbSNP: rs773920155
rs773920155
0.925 0.120 16 2061946 stop gained G/A;T snv 4.0E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 0
dbSNP: rs1057519730
rs1057519730
1.000 0.040 15 66436786 missense variant T/A;G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2009 2009
dbSNP: rs1057519817
rs1057519817
12 56088073 missense variant C/A;G snv 4.0E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2013 2013
dbSNP: rs1057519819
rs1057519819
0.851 0.240 15 66436750 missense variant T/C snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2009 2009
dbSNP: rs1057519820
rs1057519820
15 66436810 missense variant A/C snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2009 2009
dbSNP: rs1057519821
rs1057519821
15 66436814 missense variant G/C;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2009 2009
dbSNP: rs1057519822
rs1057519822
0.925 0.080 15 66481818 missense variant T/A snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2009 2009
dbSNP: rs1057519836
rs1057519836
3 41224630 missense variant A/C;G;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs1057519838
rs1057519838
0.882 0.160 5 68293790 stop gained C/T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs1057519839
rs1057519839
5 68295257 missense variant G/T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs1057519840
rs1057519840
5 68295257 inframe deletion GACAAACGTATGAACAGC/- del
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs1057519841
rs1057519841
0.925 0.120 5 68295269 missense variant A/G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs1057519842
rs1057519842
5 68295304 inframe deletion CGA/- delins
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs1057519843
rs1057519843
APC
5 112839522 frameshift variant AAGATTGGAAC/- del
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs1057519844
rs1057519844
APC
5 112839522 frameshift variant AAGATTGGAACTAGGTCAGC/- del
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs1057519845
rs1057519845
APC
5 112839990 frameshift variant GGACC/- del
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs1057519846
rs1057519846
APC
5 112840263 frameshift variant ATTGATTC/- del
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs1057519849
rs1057519849
8 127738386 missense variant C/T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs1057519850
rs1057519850
8 127738447 missense variant C/T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014
dbSNP: rs1057519851
rs1057519851
MYC
8 127738995 missense variant C/G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.700 1.000 1 2014 2014