Source: UNIPROT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs80338797
RAF1
0.827 0.160 3 12584624 missense variant G/C;T snv 2
rs104894364
KRAS
0.925 0.160 12 25227351 missense variant G/A snv 1
rs121434594
RAF1
0.827 0.160 3 12604189 missense variant G/A;C;T snv 1
rs121918469
PTPN11
0.882 0.160 12 112488454 missense variant G/C snv 1
rs121918470
PTPN11
0.790 0.160 12 112489105 missense variant A/C;G snv 4.0E-06 1
rs193929331
KRAS
0.925 0.160 12 25245372 missense variant T/C snv 1
rs267606920
NRAS
0.882 0.160 1 114713911 missense variant C/T snv 7.0E-06 1
rs267606921
NRAS
0.882 0.160 1 114713941 missense variant G/A snv 1
rs267607080
SOS1
0.925 0.160 2 39023134 missense variant A/G snv 1
rs397507501
PTPN11
0.882 0.160 12 112446385 missense variant A/G snv 1
rs397507517
PTPN11
0.827 0.160 12 112450497 missense variant A/C snv 1
rs397507523
PTPN11
0.882 0.160 12 112472954 missense variant A/G snv 1
rs397507525
PTPN11
0.925 0.160 12 112472968 missense variant C/T snv 7.0E-06 1
rs397507529
PTPN11
0.851 0.160 12 112473031 missense variant A/G snv 7.0E-06 1
rs397507539
PTPN11
0.851 0.160 12 112489047 missense variant C/A;G;T snv 4.0E-06 1
rs397507541
PTPN11
0.827 0.160 12 112489068 missense variant C/T snv 4.0E-06 7.0E-06 1
rs397507543
PTPN11
0.925 0.160 12 112489078 missense variant G/A snv 1
rs397509345
PTPN11
0.851 0.160 12 112489093 missense variant AG/CC mnv 1
rs397516815
RAF1
0.925 0.160 3 12585760 missense variant T/C snv 1
rs397516826
RAF1
0.925 0.160 3 12604202 missense variant C/A;G snv 1
rs397516827
RAF1
0.882 0.160 3 12604194 missense variant G/A;C;T snv 1
rs397516828
RAF1
0.925 0.160 3 12604188 missense variant G/A;C snv 1
rs397516830
RAF1
0.827 0.160 3 12604182 missense variant A/C;G;T snv 1
rs397517150
SOS1
0.827 0.160 2 39023118 missense variant A/C;G snv 1
rs397517153
SOS1
0.925 0.160 2 39022779 missense variant A/C;G snv 4.0E-06 1