Driver Oncogenic Mutation | Cell Line | Known Oncogenic Alterations |
---|---|---|
Wild type for BRAF and NRAS | M230 | KIT L576P |
M257 | CDKN2A R80 | |
BRAF amplification | ||
M285 | None detected | |
M368 | None detected | |
M375 | None detected | |
NRAS Mutants | M202 | NRAS Q61L |
EGFR amplification | ||
CDKN2A homozygous deletion | ||
M207 | NRAS Q61L | |
MITF amplification | ||
EGFR L747_P753 > S | ||
PTEN heterozygous deletion | ||
M243 | NRASQ61H homozygous | |
PTENE156G heterozygous | ||
CTNNB1_D32Y | ||
M245 | NRASQ61K heterozygous | |
TP53 R273H | ||
M244 | NRASQ61K heterozygous | |
M296 | NRASQ61R heterozygous | |
M318 | NRASQ61L heterozygous | |
PIK3CA C420R | ||
SBCL2 | NRASQ61K homozygous | |
Wn1366 | NRASQ61L heterozygous | |
BRAF mutants | M229 | BRAFV600E homozygous |
BRAF amplification | ||
MITF amplification | ||
AKT1 amplification | ||
PTEN heterozygous deletion | ||
M233 | BRAFV600E heterozygous | |
BRAF amplification | ||
AKT1 amplification | ||
CCND1 amplification | ||
EGFR amplification | ||
CDKN2A homozygous deletion | ||
PTEN homozygous deletion | ||
M238 | BRAFV600E heterozygous1 | |
CDKN2A homozygous deletion | ||
PTEN heterozygous deletion | ||
M249 | BRAFV600E heterozygous | |
BRAF amplification | ||
MITF amplification | ||
AKT2 amplification | ||
PTEN homozygous deletion | ||
M255 | BRAFV600E heterozygous | |
AKT2 amplification | ||
CCND1 amplification | ||
EGFR amplification | ||
CDKN2A homozygous deletion | ||
M262 | BRAFV600E homozygous | |
AKT1 E17K | ||
AKT1 amplification | ||
EGFR amplification | ||
CDKN2A homozygous deletion | ||
M263 | BRAFV600E heterozygous | |
CDKN2A heterozygous deletion | ||
M275 | BRAFV600E heterozygous | |
M297 | BRAFV600E homozygous | |
PTENG165X homozygous | ||
M299 | BRAFV600E heterozygous | |
M308 | BRAFV600E heterozygous | |
BRAF amplification | ||
MITF amplification | ||
AKT2 amplification | ||
EGFR amplification | ||
CDKN2A heterozygous deletion | ||
SKmel28 | BRAFV600E homozygous | |
EGFR P753S | ||
MITF amplification | ||
CCND1 amplification | ||
CDKN2A heterozygous deletion | ||
PTEN heterozygous deletion | ||
GNAQ or GNA11 | Mel20-06-039 | GNAQQ209L heterozygous |
 | Mel20-06-045 | GNAQQ209P heterozygous |
 | Mel20-07-070 | GNA11Q209L heterozygous |
 | Mel20-08-128 | GNA11Q209L heterozygous |
 | Mel20-09-196 | GNAQQ209P heterozygous |