Mutation - TCGA |
Type | Chromosome | Start Position | End Position | Strand | Variant Classification | Variant Type | Reference Allele | Tumor_seq Allele 1 | Tumor_seq Allele 2 | Tumor Sample Barcode | Matched Norm Sample Barcode | Genome Change | cDNA Change | Codon Change | Protein Change |
BLCA | 11 | 5655897 | 5655897 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-DK-A6AW-01A-11D-A30E-08 | TCGA-DK-A6AW-10A-01D-A30H-08 | g.chr11:5655897G>T | c.556G>T | c.(556-558)Gaa>Taa | p.E186* |
BLCA | 11 | 5656005 | 5656005 | + | Missense_Mutation | SNP | G | G | C | TCGA-UY-A78O-01A-12D-A339-08 | TCGA-UY-A78O-10A-01D-A339-08 | g.chr11:5656005G>C | c.664G>C | c.(664-666)Gag>Cag | p.E222Q |
BLCA | 11 | 5664543 | 5664543 | + | Missense_Mutation | SNP | G | G | C | TCGA-BT-A20T-01A-11D-A14W-08 | TCGA-BT-A20T-11A-11D-A14W-08 | g.chr11:5664543G>C | c.1071G>C | c.(1069-1071)aaG>aaC | p.K357N |
BRCA | 11 | 5653667 | 5653667 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-BH-A18G-01A-11D-A12B-09 | TCGA-BH-A18G-10A-01D-A12B-09 | g.chr11:5653667C>T | c.106C>T | c.(106-108)Cga>Tga | p.R36* |
BRCA | 11 | 5655085 | 5655085 | + | Missense_Mutation | SNP | G | G | A | TCGA-AC-A3TM-01A-11D-A228-09 | TCGA-AC-A3TM-10A-01D-A22A-09 | g.chr11:5655085G>A | c.475G>A | c.(475-477)Gag>Aag | p.E159K |
CESC | 11 | 5655130 | 5655130 | + | Splice_Site | SNP | G | G | T | TCGA-EA-A439-01A-11D-A243-09 | TCGA-EA-A439-10A-01D-A243-09 | g.chr11:5655130G>T | | c.e3+1 | |
CESC | 11 | 5655906 | 5655906 | + | Missense_Mutation | SNP | C | C | A | TCGA-C5-A1BQ-01C-11D-A20U-09 | TCGA-C5-A1BQ-10A-01D-A20U-09 | g.chr11:5655906C>A | c.565C>A | c.(565-567)Cag>Aag | p.Q189K |
COAD | 11 | 5653722 | 5653722 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3811-01A-01W-0995-10 | TCGA-AA-3811-10A-01W-0995-10 | g.chr11:5653722G>T | c.161G>T | c.(160-162)aGc>aTc | p.S54I |
COAD | 11 | 5653739 | 5653739 | + | Missense_Mutation | SNP | G | G | A | TCGA-G4-6293-01A-11D-1719-10 | TCGA-G4-6293-10A-01D-1719-10 | g.chr11:5653739G>A | c.178G>A | c.(178-180)Ggt>Agt | p.G60S |
COAD | 11 | 5653739 | 5653739 | + | Missense_Mutation | SNP | G | G | T | TCGA-D5-6533-01A-11D-1719-10 | TCGA-D5-6533-10A-01D-1719-10 | g.chr11:5653739G>T | c.178G>T | c.(178-180)Ggt>Tgt | p.G60C |
COAD | 11 | 5653741 | 5653741 | + | Silent | SNP | T | T | A | TCGA-CM-5868-01A-01D-1650-10 | TCGA-CM-5868-10A-01D-1650-10 | g.chr11:5653741T>A | c.180T>A | c.(178-180)ggT>ggA | p.G60G |
COAD | 11 | 5653756 | 5653756 | + | Silent | SNP | T | T | C | TCGA-CM-4743-01A-01D-1719-10 | TCGA-CM-4743-10A-01D-1719-10 | g.chr11:5653756T>C | c.195T>C | c.(193-195)ttT>ttC | p.F65F |
COAD | 11 | 5653768 | 5653768 | + | Silent | SNP | G | G | A | TCGA-CM-5861-01A-01D-1650-10 | TCGA-CM-5861-10A-01D-1650-10 | g.chr11:5653768G>A | c.207G>A | c.(205-207)caG>caA | p.Q69Q |
COAD | 11 | 5653882 | 5653882 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr11:5653882C>A | c.321C>A | c.(319-321)ttC>ttA | p.F107L |
COAD | 11 | 5663655 | 5663655 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-CM-6674-01A-11D-1835-10 | TCGA-CM-6674-10A-01D-1835-10 | g.chr11:5663655delA | c.793delA | c.(793-795)aaafs | p.K266fs |
COAD | 11 | 5663678 | 5663678 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr11:5663678G>T | c.816G>T | c.(814-816)aaG>aaT | p.K272N |
COAD | 11 | 5663738 | 5663738 | + | Splice_Site | SNP | T | T | C | TCGA-DM-A1HB-01A-21D-A183-10 | TCGA-DM-A1HB-10A-01D-A183-10 | g.chr11:5663738T>C | | c.e6+2 | |
COAD | 11 | 5664517 | 5664517 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A01Z-01A-11W-A096-10 | TCGA-AA-A01Z-11A-11W-A096-10 | g.chr11:5664517C>T | c.1045C>T | c.(1045-1047)Cat>Tat | p.H349Y |
COAD | 11 | 5664659 | 5664659 | + | Missense_Mutation | SNP | G | G | T | TCGA-AY-6196-01A-11D-1719-10 | TCGA-AY-6196-10A-01D-1719-10 | g.chr11:5664659G>T | c.1187G>T | c.(1186-1188)gGc>gTc | p.G396V |
COAD | 11 | 5664810 | 5664810 | + | Missense_Mutation | SNP | T | T | G | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr11:5664810T>G | c.1338T>G | c.(1336-1338)ttT>ttG | p.F446L |
COADREAD | 11 | 5653722 | 5653722 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3811-01A-01W-0995-10 | TCGA-AA-3811-10A-01W-0995-10 | g.chr11:5653722G>T | c.161G>T | c.(160-162)aGc>aTc | p.S54I |
COADREAD | 11 | 5653739 | 5653739 | + | Missense_Mutation | SNP | G | G | A | TCGA-G4-6293-01A-11D-1719-10 | TCGA-G4-6293-10A-01D-1719-10 | g.chr11:5653739G>A | c.178G>A | c.(178-180)Ggt>Agt | p.G60S |
COADREAD | 11 | 5653739 | 5653739 | + | Missense_Mutation | SNP | G | G | T | TCGA-D5-6533-01A-11D-1719-10 | TCGA-D5-6533-10A-01D-1719-10 | g.chr11:5653739G>T | c.178G>T | c.(178-180)Ggt>Tgt | p.G60C |
COADREAD | 11 | 5653741 | 5653741 | + | Silent | SNP | T | T | A | TCGA-CM-5868-01A-01D-1650-10 | TCGA-CM-5868-10A-01D-1650-10 | g.chr11:5653741T>A | c.180T>A | c.(178-180)ggT>ggA | p.G60G |
COADREAD | 11 | 5653741 | 5653741 | + | Silent | SNP | T | T | C | TCGA-AG-3742-01A-11D-1657-10 | TCGA-AG-3742-11A-01D-1657-10 | g.chr11:5653741T>C | c.180T>C | c.(178-180)ggT>ggC | p.G60G |
COADREAD | 11 | 5653756 | 5653756 | + | Silent | SNP | T | T | C | TCGA-CM-4743-01A-01D-1719-10 | TCGA-CM-4743-10A-01D-1719-10 | g.chr11:5653756T>C | c.195T>C | c.(193-195)ttT>ttC | p.F65F |
COADREAD | 11 | 5653768 | 5653768 | + | Silent | SNP | G | G | A | TCGA-CM-5861-01A-01D-1650-10 | TCGA-CM-5861-10A-01D-1650-10 | g.chr11:5653768G>A | c.207G>A | c.(205-207)caG>caA | p.Q69Q |
COADREAD | 11 | 5653882 | 5653882 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr11:5653882C>A | c.321C>A | c.(319-321)ttC>ttA | p.F107L |
COADREAD | 11 | 5663655 | 5663655 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-CM-6674-01A-11D-1835-10 | TCGA-CM-6674-10A-01D-1835-10 | g.chr11:5663655delA | c.793delA | c.(793-795)aaafs | p.K266fs |
COADREAD | 11 | 5663678 | 5663678 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr11:5663678G>T | c.816G>T | c.(814-816)aaG>aaT | p.K272N |
COADREAD | 11 | 5663738 | 5663738 | + | Splice_Site | SNP | T | T | C | TCGA-DM-A1HB-01A-21D-A183-10 | TCGA-DM-A1HB-10A-01D-A183-10 | g.chr11:5663738T>C | | c.e6+2 | |
COADREAD | 11 | 5664517 | 5664517 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A01Z-01A-11W-A096-10 | TCGA-AA-A01Z-11A-11W-A096-10 | g.chr11:5664517C>T | c.1045C>T | c.(1045-1047)Cat>Tat | p.H349Y |
COADREAD | 11 | 5664659 | 5664659 | + | Missense_Mutation | SNP | G | G | T | TCGA-AY-6196-01A-11D-1719-10 | TCGA-AY-6196-10A-01D-1719-10 | g.chr11:5664659G>T | c.1187G>T | c.(1186-1188)gGc>gTc | p.G396V |
COADREAD | 11 | 5664810 | 5664810 | + | Missense_Mutation | SNP | T | T | G | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr11:5664810T>G | c.1338T>G | c.(1336-1338)ttT>ttG | p.F446L |
DLBC | 11 | 5653866 | 5653866 | + | Missense_Mutation | SNP | A | A | G | TCGA-G8-6909-01A-11D-2210-10 | TCGA-G8-6909-14A-01D-2210-10 | g.chr11:5653866A>G | c.305A>G | c.(304-306)gAg>gGg | p.E102G |
DLBC | 11 | 5664047 | 5664047 | + | Splice_Site | SNP | A | A | G | TCGA-FF-8042-01A-11D-2210-10 | TCGA-FF-8042-10A-01D-2210-10 | g.chr11:5664047A>G | c.875A>G | c.(874-876)gAa>gGa | p.E292G |
ESCA | 11 | 5655862 | 5655862 | + | Splice_Site | SNP | A | A | T | TCGA-LN-A8HZ-01A-11D-A36J-09 | TCGA-LN-A8HZ-10A-01D-A36M-09 | g.chr11:5655862A>T | c.521A>T | c.(520-522)tAt>tTt | p.Y174F |
ESCA | 11 | 5655908 | 5655908 | + | Silent | SNP | G | G | A | TCGA-Q9-A6FU-01A-11D-A31U-09 | TCGA-Q9-A6FU-10A-01D-A31U-09 | g.chr11:5655908G>A | c.567G>A | c.(565-567)caG>caA | p.Q189Q |
GBM | 11 | 5656037 | 5656037 | + | Missense_Mutation | SNP | G | G | T | TCGA-26-1442-01A-01D-1696-08 | TCGA-26-1442-10A-01D-1696-08 | g.chr11:5656037G>T | c.696G>T | c.(694-696)gaG>gaT | p.E232D |
GBMLGG | 11 | 5655971 | 5655971 | + | Missense_Mutation | SNP | G | G | C | TCGA-TM-A84Q-01A-11D-A36O-08 | TCGA-TM-A84Q-10A-01D-A367-08 | g.chr11:5655971G>C | c.630G>C | c.(628-630)aaG>aaC | p.K210N |
GBMLGG | 11 | 5656037 | 5656037 | + | Missense_Mutation | SNP | G | G | T | TCGA-26-1442-01A-01D-1696-08 | TCGA-26-1442-10A-01D-1696-08 | g.chr11:5656037G>T | c.696G>T | c.(694-696)gaG>gaT | p.E232D |
HNSC | 11 | 5653605 | 5653605 | + | Missense_Mutation | SNP | G | G | A | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr11:5653605G>A | c.44G>A | c.(43-45)tGt>tAt | p.C15Y |
HNSC | 11 | 5653889 | 5653889 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-CR-7371-01A-11D-2012-08 | TCGA-CR-7371-10A-01D-2013-08 | g.chr11:5653889G>T | c.328G>T | c.(328-330)Gag>Tag | p.E110* |
HNSC | 11 | 5655105 | 5655105 | + | Silent | SNP | C | C | A | TCGA-RS-A6TO-01A-32D-A34J-08 | TCGA-RS-A6TO-10A-01D-A34M-08 | g.chr11:5655105C>A | c.495C>A | c.(493-495)atC>atA | p.I165I |
HNSC | 11 | 5655876 | 5655876 | + | Missense_Mutation | SNP | G | G | A | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr11:5655876G>A | c.535G>A | c.(535-537)Gag>Aag | p.E179K |
HNSC | 11 | 5656091 | 5656091 | + | Splice_Site | SNP | G | G | C | TCGA-CR-7388-01A-11D-2012-08 | TCGA-CR-7388-10A-01D-2013-08 | g.chr11:5656091G>C | c.750G>C | c.(748-750)caG>caC | p.Q250H |
HNSC | 11 | 5664829 | 5664829 | + | Missense_Mutation | SNP | G | G | A | TCGA-BA-A6DI-01A-11D-A30E-08 | TCGA-BA-A6DI-10A-01D-A30H-08 | g.chr11:5664829G>A | c.1357G>A | c.(1357-1359)Ggc>Agc | p.G453S |
KICH | 11 | 5655127 | 5655127 | + | Missense_Mutation | SNP | A | A | G | TCGA-KN-8428-01A-11D-2310-10 | TCGA-KN-8428-11A-01D-2311-10 | g.chr11:5655127A>G | c.517A>G | c.(517-519)Aag>Gag | p.K173E |
KIPAN | 11 | 5653647 | 5653647 | + | Missense_Mutation | SNP | A | A | T | TCGA-CZ-4862-01A-01D-1373-10 | TCGA-CZ-4862-11A-01D-1373-10 | g.chr11:5653647A>T | c.86A>T | c.(85-87)gAc>gTc | p.D29V |
KIPAN | 11 | 5655127 | 5655127 | + | Missense_Mutation | SNP | A | A | G | TCGA-KN-8428-01A-11D-2310-10 | TCGA-KN-8428-11A-01D-2311-10 | g.chr11:5655127A>G | c.517A>G | c.(517-519)Aag>Gag | p.K173E |
KIPAN | 11 | 5655129 | 5655129 | + | Splice_Site | SNP | G | G | C | TCGA-CJ-5676-01A-11D-1534-10 | TCGA-CJ-5676-11A-01D-1534-10 | g.chr11:5655129G>C | c.519G>C | c.(517-519)aaG>aaC | p.K173N |
KIRC | 11 | 5653647 | 5653647 | + | Missense_Mutation | SNP | A | A | T | TCGA-CZ-4862-01A-01D-1373-10 | TCGA-CZ-4862-11A-01D-1373-10 | g.chr11:5653647A>T | c.86A>T | c.(85-87)gAc>gTc | p.D29V |
KIRC | 11 | 5655129 | 5655129 | + | Splice_Site | SNP | G | G | C | TCGA-CJ-5676-01A-11D-1534-10 | TCGA-CJ-5676-11A-01D-1534-10 | g.chr11:5655129G>C | c.519G>C | c.(517-519)aaG>aaC | p.K173N |
LGG | 11 | 5655971 | 5655971 | + | Missense_Mutation | SNP | G | G | C | TCGA-TM-A84Q-01A-11D-A36O-08 | TCGA-TM-A84Q-10A-01D-A367-08 | g.chr11:5655971G>C | c.630G>C | c.(628-630)aaG>aaC | p.K210N |
LIHC | 11 | 5653572 | 5653572 | + | Missense_Mutation | SNP | A | A | G | TCGA-DD-AAD3-01A-11D-A40R-10 | TCGA-DD-AAD3-10A-01D-A40U-10 | g.chr11:5653572A>G | c.11A>G | c.(10-12)aAa>aGa | p.K4R |
LIHC | 11 | 5664784 | 5664784 | + | Missense_Mutation | SNP | G | G | A | TCGA-G3-A3CG-01A-11D-A20W-10 | TCGA-G3-A3CG-10A-01D-A20W-10 | g.chr11:5664784G>A | c.1312G>A | c.(1312-1314)Gac>Aac | p.D438N |
LUAD | 11 | 5653697 | 5653697 | + | Missense_Mutation | SNP | G | G | A | TCGA-05-4382-01A-01D-1931-08 | TCGA-05-4382-10A-01D-1265-08 | g.chr11:5653697G>A | c.136G>A | c.(136-138)Gca>Aca | p.A46T |
LUAD | 11 | 5655032 | 5655032 | + | Splice_Site | SNP | A | A | T | TCGA-17-Z045-01A-01W-0746-08 | TCGA-17-Z045-11A-01W-0747-08 | g.chr11:5655032A>T | | c.e3-1 | |
LUSC | 11 | 5663637 | 5663637 | + | Splice_Site | SNP | A | A | G | TCGA-56-6546-01A-11D-1817-08 | TCGA-56-6546-10A-01D-1817-08 | g.chr11:5663637A>G | c.775A>G | c.(775-777)Agt>Ggt | p.S259G |
LUSC | 11 | 5664869 | 5664869 | + | Missense_Mutation | SNP | A | A | T | TCGA-34-5239-01A-21D-1817-08 | TCGA-34-5239-10A-01D-1817-08 | g.chr11:5664869A>T | c.1397A>T | c.(1396-1398)cAg>cTg | p.Q466L |
OV | 11 | 5653739 | 5653739 | + | Missense_Mutation | SNP | G | G | C | TCGA-09-2050-01A-01W-0799-08 | TCGA-09-2050-10A-01W-0799-08 | g.chr11:5653739G>C | c.178G>C | c.(178-180)Ggt>Cgt | p.G60R |
READ | 11 | 5653741 | 5653741 | + | Silent | SNP | T | T | C | TCGA-AG-3742-01A-11D-1657-10 | TCGA-AG-3742-11A-01D-1657-10 | g.chr11:5653741T>C | c.180T>C | c.(178-180)ggT>ggC | p.G60G |
SKCM | 11 | 5653872 | 5653872 | + | Missense_Mutation | SNP | T | T | G | TCGA-EE-A181-06A-11D-A196-08 | TCGA-EE-A181-10A-01D-A198-08 | g.chr11:5653872T>G | c.311T>G | c.(310-312)cTc>cGc | p.L104R |
SKCM | 11 | 5655033 | 5655033 | + | Splice_Site | SNP | G | G | A | TCGA-EE-A29L-06A-12D-A196-08 | TCGA-EE-A29L-10A-01D-A198-08 | g.chr11:5655033G>A | | c.e3-1 | |
SKCM | 11 | 5655066 | 5655066 | + | Silent | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr11:5655066G>A | c.456G>A | c.(454-456)aaG>aaA | p.K152K |
SKCM | 11 | 5655114 | 5655114 | + | Silent | SNP | G | G | A | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr11:5655114G>A | c.504G>A | c.(502-504)gaG>gaA | p.E168E |
SKCM | 11 | 5664061 | 5664061 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A20C-06A-11D-A196-08 | TCGA-EE-A20C-10A-01D-A198-08 | g.chr11:5664061C>T | c.889C>T | c.(889-891)Cgg>Tgg | p.R297W |
SKCM | 11 | 5664387 | 5664387 | + | Silent | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr11:5664387G>A | c.915G>A | c.(913-915)ctG>ctA | p.L305L |
SKCM | 11 | 5664422 | 5664422 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A2JP-06A-11D-A19A-08 | TCGA-D3-A2JP-10A-01D-A19A-08 | g.chr11:5664422C>T | c.950C>T | c.(949-951)tCa>tTa | p.S317L |
SKCM | 11 | 5664531 | 5664531 | + | Silent | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr11:5664531G>A | c.1059G>A | c.(1057-1059)gtG>gtA | p.V353V |
SKCM | 11 | 5664584 | 5664584 | + | Missense_Mutation | SNP | C | C | T | TCGA-FS-A1ZZ-06A-11D-A197-08 | TCGA-FS-A1ZZ-10A-01D-A199-08 | g.chr11:5664584C>T | c.1112C>T | c.(1111-1113)tCc>tTc | p.S371F |
SKCM | 11 | 5664713 | 5664713 | + | Missense_Mutation | SNP | C | C | T | TCGA-ER-A3PL-06A-11D-A23B-08 | TCGA-ER-A3PL-10A-01D-A23B-08 | g.chr11:5664713C>T | c.1241C>T | c.(1240-1242)tCt>tTt | p.S414F |
SKCM | 11 | 5664746 | 5664746 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A2JH-06A-11D-A196-08 | TCGA-D3-A2JH-10A-01D-A198-08 | g.chr11:5664746C>T | c.1274C>T | c.(1273-1275)tCc>tTc | p.S425F |
SKCM | 11 | 5664747 | 5664747 | + | Silent | SNP | C | C | T | TCGA-D3-A2JH-06A-11D-A196-08 | TCGA-D3-A2JH-10A-01D-A198-08 | g.chr11:5664747C>T | c.1275C>T | c.(1273-1275)tcC>tcT | p.S425S |
SKCM | 11 | 5664747 | 5664747 | + | Silent | SNP | C | C | T | TCGA-ER-A42L-06A-11D-A24R-08 | TCGA-ER-A42L-10A-01D-A24R-08 | g.chr11:5664747C>T | c.1275C>T | c.(1273-1275)tcC>tcT | p.S425S |
SKCM | 11 | 5664813 | 5664813 | + | Silent | SNP | C | C | T | TCGA-EE-A3J5-06A-11D-A20D-08 | TCGA-EE-A3J5-10A-01D-A20D-08 | g.chr11:5664813C>T | c.1341C>T | c.(1339-1341)ttC>ttT | p.F447F |
BLCA | 11 | 5653496 | 5653496 | + | 5'UTR | SNP | T | T | C | TCGA-ZF-A9RF-01A-11D-A38G-08 | TCGA-ZF-A9RF-10A-01D-A38J-08 | g.chr11:5653496T>C | | | |
COAD | 11 | 5653546 | 5653546 | + | 5'UTR | SNP | C | C | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr11:5653546C>T | | | |
COAD | 11 | 5653546 | 5653546 | + | 5'UTR | SNP | C | C | T | TCGA-AD-6964-01A-11D-1924-10 | TCGA-AD-6964-10A-01D-1924-10 | g.chr11:5653546C>T | | | |
COADREAD | 11 | 5653546 | 5653546 | + | 5'UTR | SNP | C | C | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr11:5653546C>T | | | |
COADREAD | 11 | 5653546 | 5653546 | + | 5'UTR | SNP | C | C | T | TCGA-AD-6964-01A-11D-1924-10 | TCGA-AD-6964-10A-01D-1924-10 | g.chr11:5653546C>T | | | |
HNSC | 11 | 5653492 | 5653492 | + | 5'UTR | DEL | G | G | - | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr11:5653492delG | | | |
SKCM | 11 | 5653515 | 5653515 | + | 5'UTR | SNP | G | G | A | TCGA-GN-A4U3-06A-11D-A32N-08 | TCGA-GN-A4U3-10F-01D-A32N-08 | g.chr11:5653515G>A | | | |