Source: UNIPROT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs869025606
BRAF
1.000 0.160 7 140781609 missense variant A/C snv 1
rs387907205
KRAS
0.925 0.160 12 25227313 missense variant A/C;G snv 1
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 1
rs121434498
MAP2K2
0.807 0.280 19 4117553 missense variant A/C;G;T snv 1
rs869025340
BRAF
0.925 0.160 7 140777032 missense variant A/C;G;T snv 1
rs121913341
BRAF
0.851 0.280 7 140753350 missense variant A/C;T snv 2
rs121434497
MAP2K2
0.925 0.160 19 4117552 missense variant A/C;T snv 1
rs180177042
BRAF
0.807 0.280 7 140749365 missense variant A/C;T snv 1
rs121434499
MAP2K2
0.925 0.160 19 4110559 missense variant A/G snv 1
rs121908595
MAP2K1
0.827 0.280 15 66436843 missense variant A/G snv 4.0E-06 1
rs397507473
BRAF
1.000 0.160 7 140781605 missense variant A/G snv 4.0E-06 1
rs180177036
BRAF
0.925 0.200 7 140778053 missense variant C/A;G snv 1
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 5
rs121913355
BRAF
0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 4
rs104894229
LRRC56 ; HRAS
0.564 0.600 11 534289 missense variant C/A;G;T snv 1
rs121913348
BRAF
0.763 0.480 7 140781617 missense variant C/A;G;T snv 1
rs397507483
BRAF
0.790 0.400 7 140753348 missense variant C/A;T snv 1
rs180177034
BRAF
0.882 0.200 7 140801536 missense variant C/G snv 1
rs104894359
KRAS
0.851 0.200 12 25227346 missense variant C/G;T snv 2
rs104894365
KRAS
0.827 0.320 12 25245345 missense variant C/T snv 1
rs397517147
SOS1
0.882 0.200 2 39023131 missense variant C/T snv 4.0E-06 1
rs104894366
KRAS
0.776 0.400 12 25245284 missense variant G/A;C snv 2
rs121913369
BRAF
0.790 0.280 7 140753346 missense variant G/A;C snv 4.0E-06 1
rs121913375
BRAF
0.851 0.240 7 140753339 missense variant G/A;C snv 1
rs267607230
MAP2K2
0.925 0.160 19 4110576 missense variant G/A;C;T snv 1