Gene/Event | Cancer Type | Patient | Variant | Mutation Level |
---|---|---|---|---|
COL21A1 | Breast Cancer | p123_case9 | p.K697fs | Trunk mutation |
COL21A1 | Breast Cancer | p143_p4 | Chr6:55940295:T>C | Private mutation |
COL21A1 | Colorectal Cancer | p014_CRC2 | p.R850G | Trunk mutation |
COL21A1 | Colorectal Cancer | p034_MSU1 | Chr6:55940294-55940295:CT>C | Private mutation |
COL21A1 | Colorectal Cancer | p155_p252 | p.M688K | Private mutation |
COL21A1 | Colorectal Cancer | p155_p252 | p.X620_splice | Private mutation |
COL21A1 | Gastric Adenocarcinoma | p011_MSS3 | p.S93I | Private mutation |
COL21A1 | Gastric Carcinoma | p106_GC04 | p.G722G | Trunk mutation |
COL21A1 | Glioblastoma | p113_case01 | p.D227N | Private mutation |
COL21A1 | Glioblastoma | p113_case02 | p.Q414L | Private mutation |
COL21A1 | Glioblastoma | p113_case36 | p.A946T | Private mutation |
COL21A1 | Glioma | p168_P18 | p.A559T | Private mutation |
COL21A1 | Glioma | p168_P18 | p.E422K | Private mutation |
COL21A1 | Hepatocellular Carcinoma | p061_P02 | Chr6:55922459:T>C | Trunk mutation |
COL21A1 | Hepatocellular Carcinoma | p061_P10 | Chr6:55922611:T>C | Trunk mutation |
COL21A1 | Lung Adenocarcinoma | p017_4990 | Chr6:55924746:G>A | Branch mutation |
COL21A1 | Melanoma | p043_A | p.E90K | Private mutation |
COL21A1 | Melanoma | p043_F | p.G385R | Trunk mutation |
COL21A1 | Melanoma | p043_G | p.G608E | Trunk mutation |
COL21A1 | Melanoma | p043_G | p.R151Q | Trunk mutation |
COL21A1 | Ovarian Cancer | p144_AOCS064 | p.D43H | Trunk mutation |
COL21A1 | Ovarian Cancer | p144_AOCS093 | p.V316V | Private mutation |
COL21A1 | Ovarian Cancer | p144_AOCS093 | p.V316G | Private mutation |
COL21A1 | Prostate Cancer | p116_PS286 | p.A552T | Private mutation |
COL21A1 | Prostate Cancer | p117_PrCa06 | p.T116A | Trunk mutation |
COL21A1 | Renal Cell Carcinoma | p073_RCC3 | Chr6:55923836:T>C | Branch mutation |
COL21A1 | Renal Cell Carcinoma | p073_RCC5 | Chr6:56047564:C>G | Private mutation |
COL21A1 | Urothelial Carcinoma | p031_WCM077 | p.P848P | Private mutation |