Gene Name | HGNC ID | COSMIC_MutID | Primary site | Primary histology | AA-Mutation | Mutation Type | Genomic Position | FATHMM prediction | FATHMM score | Literature evidence |
CHUK | 1974 | COSM4989885, | skin | carcinoma | p.P190L | Substitution - Missense | 10:100219128-100219128, | PATHOGENIC | 0.998 | 25589618 |
CHUK | 1974 | COSM6164, | breast | carcinoma | p.? | Unknown | 10:100207333-100207333, | PATHOGENIC | 0.9974 | 15908952 |
CHUK | 1974 | COSM4989884, | skin | carcinoma | p.S266N | Substitution - Missense | 10:100218718-100218718, | PATHOGENIC | 0.99298 | 25589618 |
CHUK | 1974 | COSM20985, | central_nervous_system | glioma | p.? | Unknown | 10:100202087-100202087, | PATHOGENIC | 0.98603 | Info_not_available |
CHUK | 1974 | COSM20985, | central_nervous_system | glioma | p.? | Unknown | 10:100202087-100202087, | PATHOGENIC | 0.98603 | Info_not_available |
CHUK | 1974 | COSM4989887, | skin | carcinoma | p.? | Unknown | 10:100222981-100222981, | PATHOGENIC | 0.97984 | 25589618 |
CHUK | 1974 | COSM13312, | central_nervous_system | glioma | p.R133* | Substitution - Nonsense | 10:100220665-100220665, | PATHOGENIC | 0.97771 | 16618716 |
CHUK | 1974 | COSM13312, | large_intestine | carcinoma | p.R133* | Substitution - Nonsense | 10:100220665-100220665, | PATHOGENIC | 0.97771 | Info_not_available |
CHUK | 1974 | COSM13312, | central_nervous_system | glioma | p.R133* | Substitution - Nonsense | 10:100220665-100220665, | PATHOGENIC | 0.97771 | 16618716 |
CHUK | 1974 | COSM13312, | large_intestine | carcinoma | p.R133* | Substitution - Nonsense | 10:100220665-100220665, | PATHOGENIC | 0.97771 | Info_not_available |
CHUK | 1974 | COSM3751488, | soft_tissue | haemangioblastoma | p.S486S | Substitution - coding silent | 10:100204555-100204555, | PATHOGENIC | 0.94889 | 25589003 |
CHUK | 1974 | COSM3751488, | soft_tissue | haemangioblastoma | p.S486S | Substitution - coding silent | 10:100204555-100204555, | PATHOGENIC | 0.94889 | 25589003 |
CHUK | 1974 | COSM5703421, | haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm | p.Q260* | Substitution - Nonsense | 10:100218737-100218737, | PATHOGENIC | 0.94437 | 26437031 |
CHUK | 1974 | COSM4989886, | skin | carcinoma | p.L152F | Substitution - Missense | 10:100220608-100220608, | PATHOGENIC | 0.93547 | 25589618 |
CHUK | 1974 | COSM3433515, | skin | carcinoma | p.S336L | Substitution - Missense | 10:100209716-100209716, | PATHOGENIC | 0.92668 | 25589618 |
CHUK | 1974 | COSM4989883, | skin | carcinoma | p.Q285* | Substitution - Nonsense | 10:100218075-100218075, | PATHOGENIC | 0.91687 | 25589618 |
CHUK | 1974 | COSM304613, | salivary_gland | carcinoma | p.R104* | Substitution - Nonsense | 10:100222871-100222871, | PATHOGENIC | 0.91389 | 27334835 |
CHUK | 1974 | COSM304613, | large_intestine | carcinoma | p.R104* | Substitution - Nonsense | 10:100222871-100222871, | PATHOGENIC | 0.91389 | 21892161 |
CHUK | 1974 | COSM4989882, | skin | carcinoma | p.I470I | Substitution - coding silent | 10:100204603-100204603, | PATHOGENIC | 0.91072 | 25589618 |
CHUK | 1974 | COSM147026, | soft_tissue | haemangioblastoma | p.V155A | Substitution - Missense | 10:100220598-100220598, | PATHOGENIC | 0.90637 | 25589003 |
CHUK | 1974 | COSM2057796, | central_nervous_system | glioma | p.R646fs*22 | Deletion - Frameshift | 10:100194022-100194022, | Info_not_available | Info_not_available | 26487540 |
CHUK | 1974 | COSM5967328, | salivary_gland | carcinoma | p.C178fs*16 | Deletion - Frameshift | 10:100219301-100219302, | Info_not_available | Info_not_available | 27334835 |