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 | 10 | 15821032 | 15821032 | + | Missense_Mutation | SNP | C | C | G | TCGA-GU-A766-01A-11D-A32B-08 | TCGA-GU-A766-10A-01D-A329-08 | g.chr10:15821032C>G | c.1297G>C | c.(1297-1299)Gag>Cag | p.E433Q |
BLCA | 10 | 15821080 | 15821080 | + | Missense_Mutation | SNP | C | C | T | TCGA-XF-AAN2-01A-11D-A42E-08 | TCGA-XF-AAN2-10A-01D-A42H-08 | g.chr10:15821080C>T | c.1249G>A | c.(1249-1251)Gat>Aat | p.D417N |
BLCA | 10 | 15858863 | 15858863 | + | Missense_Mutation | SNP | C | C | T | TCGA-UY-A9PF-01A-11D-A38G-08 | TCGA-UY-A9PF-10A-01D-A38J-08 | g.chr10:15858863C>T | c.853G>A | c.(853-855)Gag>Aag | p.E285K |
BLCA | 10 | 15863726 | 15863726 | + | Splice_Site | SNP | C | C | T | TCGA-CF-A3MI-01A-11D-A20D-08 | TCGA-CF-A3MI-10A-01D-A20D-08 | g.chr10:15863726C>T | | c.e9-1 | |
BLCA | 10 | 15875631 | 15875631 | + | Missense_Mutation | SNP | A | A | G | TCGA-GV-A3QI-01A-11D-A21Z-08 | TCGA-GV-A3QI-10A-01D-A21Z-08 | g.chr10:15875631A>G | c.728T>C | c.(727-729)aTg>aCg | p.M243T |
BLCA | 10 | 15883574 | 15883574 | + | Missense_Mutation | SNP | C | C | G | TCGA-UY-A78K-01A-11D-A339-08 | TCGA-UY-A78K-10A-01D-A339-08 | g.chr10:15883574C>G | c.260G>C | c.(259-261)tGt>tCt | p.C87S |
BLCA | 10 | 15883574 | 15883574 | + | Missense_Mutation | SNP | C | C | T | TCGA-XF-A9SU-01A-31D-A391-08 | TCGA-XF-A9SU-10A-01D-A394-08 | g.chr10:15883574C>T | c.260G>A | c.(259-261)tGt>tAt | p.C87Y |
BRCA | 10 | 15828635 | 15828635 | + | Missense_Mutation | SNP | C | C | T | TCGA-A8-A095-01A-11W-A019-09 | TCGA-A8-A095-10A-01W-A021-09 | g.chr10:15828635C>T | c.1041G>A | c.(1039-1041)atG>atA | p.M347I |
BRCA | 10 | 15838114 | 15838114 | + | Missense_Mutation | SNP | T | T | C | TCGA-D8-A1XK-01A-21D-A14K-09 | TCGA-D8-A1XK-10A-01D-A14K-09 | g.chr10:15838114T>C | c.940A>G | c.(940-942)Acc>Gcc | p.T314A |
BRCA | 10 | 15858876 | 15858876 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-A2-A0SY-01A-31D-A099-09 | TCGA-A2-A0SY-10A-01D-A099-09 | g.chr10:15858876C>T | c.840G>A | c.(838-840)tgG>tgA | p.W280* |
BRCA | 10 | 15879305 | 15879305 | + | Missense_Mutation | SNP | G | G | C | TCGA-GM-A3NW-01A-21D-A228-09 | TCGA-GM-A3NW-10A-01D-A22A-09 | g.chr10:15879305G>C | c.474C>G | c.(472-474)ttC>ttG | p.F158L |
COAD | 10 | 15824206 | 15824206 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr10:15824206G>T | c.1136C>A | c.(1135-1137)tCt>tAt | p.S379Y |
COAD | 10 | 15838151 | 15838152 | + | Frame_Shift_Ins | INS | - | - | G | TCGA-G4-6309-01A-21D-1835-10 | TCGA-G4-6309-10A-01D-1835-10 | g.chr10:15838151_15838152insG | c.902_903insC | c.(901-903)cctfs | p.P301fs |
COAD | 10 | 15863676 | 15863676 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3952-01A-01W-0995-10 | TCGA-AA-3952-10A-01W-0995-10 | g.chr10:15863676C>T | c.780G>A | c.(778-780)atG>atA | p.M260I |
COAD | 10 | 15879309 | 15879309 | + | Missense_Mutation | SNP | G | G | A | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr10:15879309G>A | c.470C>T | c.(469-471)tCg>tTg | p.S157L |
COADREAD | 10 | 15824206 | 15824206 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr10:15824206G>T | c.1136C>A | c.(1135-1137)tCt>tAt | p.S379Y |
COADREAD | 10 | 15838104 | 15838104 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr10:15838104G>A | c.950C>T | c.(949-951)cCa>cTa | p.P317L |
COADREAD | 10 | 15838151 | 15838152 | + | Frame_Shift_Ins | INS | - | - | G | TCGA-G4-6309-01A-21D-1835-10 | TCGA-G4-6309-10A-01D-1835-10 | g.chr10:15838151_15838152insG | c.902_903insC | c.(901-903)cctfs | p.P301fs |
COADREAD | 10 | 15863676 | 15863676 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3952-01A-01W-0995-10 | TCGA-AA-3952-10A-01W-0995-10 | g.chr10:15863676C>T | c.780G>A | c.(778-780)atG>atA | p.M260I |
COADREAD | 10 | 15879309 | 15879309 | + | Missense_Mutation | SNP | G | G | A | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr10:15879309G>A | c.470C>T | c.(469-471)tCg>tTg | p.S157L |
ESCA | 10 | 15876565 | 15876565 | + | Missense_Mutation | SNP | T | T | C | TCGA-R6-A8WC-01A-11D-A37C-09 | TCGA-R6-A8WC-10A-01D-A37F-09 | g.chr10:15876565T>C | c.627A>G | c.(625-627)atA>atG | p.I209M |
GBMLGG | 10 | 15876560 | 15876560 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr10:15876560G>T | c.632C>A | c.(631-633)cCt>cAt | p.P211H |
GBMLGG | 10 | 15885222 | 15885222 | + | Missense_Mutation | SNP | C | C | T | TCGA-TM-A84M-01A-11D-A36O-08 | TCGA-TM-A84M-10A-01D-A367-08 | g.chr10:15885222C>T | c.224G>A | c.(223-225)cGg>cAg | p.R75Q |
GBMLGG | 10 | 15902255 | 15902255 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr10:15902255G>A | c.44C>T | c.(43-45)aCc>aTc | p.T15I |
HNSC | 10 | 15828592 | 15828592 | + | Missense_Mutation | SNP | C | C | A | TCGA-CV-6935-01A-11D-1912-08 | TCGA-CV-6935-10A-01D-1912-08 | g.chr10:15828592C>A | c.1084G>T | c.(1084-1086)Ggc>Tgc | p.G362C |
HNSC | 10 | 15885231 | 15885231 | + | Missense_Mutation | SNP | G | G | T | TCGA-BA-A6DA-01A-31D-A31L-08 | TCGA-BA-A6DA-10A-01D-A31J-08 | g.chr10:15885231G>T | c.215C>A | c.(214-216)tCt>tAt | p.S72Y |
KIPAN | 10 | 15879243 | 15879243 | + | Missense_Mutation | SNP | A | A | G | TCGA-BP-5174-01A-01D-1429-08 | TCGA-BP-5174-11A-01D-1429-08 | g.chr10:15879243A>G | c.536T>C | c.(535-537)tTt>tCt | p.F179S |
KIPAN | 10 | 15902225 | 15902225 | + | Missense_Mutation | SNP | A | A | G | TCGA-CJ-4895-01A-01D-1373-10 | TCGA-CJ-4895-11A-01D-1373-10 | g.chr10:15902225A>G | c.74T>C | c.(73-75)aTt>aCt | p.I25T |
KIRC | 10 | 15879243 | 15879243 | + | Missense_Mutation | SNP | A | A | G | TCGA-BP-5174-01A-01D-1429-08 | TCGA-BP-5174-11A-01D-1429-08 | g.chr10:15879243A>G | c.536T>C | c.(535-537)tTt>tCt | p.F179S |
KIRC | 10 | 15902225 | 15902225 | + | Missense_Mutation | SNP | A | A | G | TCGA-CJ-4895-01A-01D-1373-10 | TCGA-CJ-4895-11A-01D-1373-10 | g.chr10:15902225A>G | c.74T>C | c.(73-75)aTt>aCt | p.I25T |
LGG | 10 | 15876560 | 15876560 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr10:15876560G>T | c.632C>A | c.(631-633)cCt>cAt | p.P211H |
LGG | 10 | 15885222 | 15885222 | + | Missense_Mutation | SNP | C | C | T | TCGA-TM-A84M-01A-11D-A36O-08 | TCGA-TM-A84M-10A-01D-A367-08 | g.chr10:15885222C>T | c.224G>A | c.(223-225)cGg>cAg | p.R75Q |
LGG | 10 | 15902255 | 15902255 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr10:15902255G>A | c.44C>T | c.(43-45)aCc>aTc | p.T15I |
LIHC | 10 | 15821138 | 15821138 | + | Silent | SNP | G | G | T | TCGA-EP-A2KA-01A-11D-A183-10 | TCGA-EP-A2KA-10A-01D-A183-10 | g.chr10:15821138G>T | c.1191C>A | c.(1189-1191)gtC>gtA | p.V397V |
LIHC | 10 | 15858832 | 15858832 | + | Splice_Site | SNP | A | A | G | TCGA-BC-A10U-01A-11D-A12Z-10 | TCGA-BC-A10U-11A-11D-A12Z-10 | g.chr10:15858832A>G | | c.e10+1 | |
LIHC | 10 | 15863696 | 15863696 | + | Missense_Mutation | SNP | C | C | G | TCGA-DD-AADF-01A-11D-A40R-10 | TCGA-DD-AADF-10A-01D-A40U-10 | g.chr10:15863696C>G | c.760G>C | c.(760-762)Gta>Cta | p.V254L |
LIHC | 10 | 15875655 | 15875655 | + | Missense_Mutation | SNP | T | T | C | TCGA-DD-AAEK-01A-11D-A40R-10 | TCGA-DD-AAEK-10A-01D-A40U-10 | g.chr10:15875655T>C | c.704A>G | c.(703-705)gAt>gGt | p.D235G |
LIHC | 10 | 15883432 | 15883432 | + | Silent | SNP | T | T | C | TCGA-EP-A2KB-01A-11D-A183-10 | TCGA-EP-A2KB-10A-01D-A183-10 | g.chr10:15883432T>C | c.402A>G | c.(400-402)gaA>gaG | p.E134E |
LUAD | 10 | 15821010 | 15821010 | + | Missense_Mutation | SNP | C | C | A | TCGA-78-8662-01A-11D-2393-08 | TCGA-78-8662-10A-01D-2393-08 | g.chr10:15821010C>A | c.1319G>T | c.(1318-1320)cGc>cTc | p.R440L |
LUAD | 10 | 15821093 | 15821093 | + | Silent | SNP | G | G | A | TCGA-05-4432-01A-01D-1265-08 | TCGA-05-4432-10A-01D-1265-08 | g.chr10:15821093G>A | c.1236C>T | c.(1234-1236)ccC>ccT | p.P412P |
LUAD | 10 | 15875667 | 15875667 | + | Missense_Mutation | SNP | G | G | A | TCGA-L4-A4E5-01A-11D-A24P-08 | TCGA-L4-A4E5-10A-01D-A24P-08 | g.chr10:15875667G>A | c.692C>T | c.(691-693)tCt>tTt | p.S231F |
LUAD | 10 | 15876551 | 15876551 | + | Missense_Mutation | SNP | C | C | T | TCGA-55-8092-01A-11D-2238-08 | TCGA-55-8092-10A-01D-2238-08 | g.chr10:15876551C>T | c.641G>A | c.(640-642)gGa>gAa | p.G214E |
LUAD | 10 | 15883599 | 15883599 | + | Splice_Site | SNP | C | C | A | TCGA-50-6594-01A-11D-1753-08 | TCGA-50-6594-11A-01D-1753-08 | g.chr10:15883599C>A | | c.e4-1 | |
LUSC | 10 | 15880243 | 15880243 | + | Missense_Mutation | SNP | A | A | G | TCGA-56-6545-01A-11D-1817-08 | TCGA-56-6545-10A-01D-1817-08 | g.chr10:15880243A>G | c.445T>C | c.(445-447)Ttt>Ctt | p.F149L |
LUSC | 10 | 15885221 | 15885221 | + | Silent | SNP | C | C | A | TCGA-85-6560-01A-11D-1817-08 | TCGA-85-6560-10A-01D-1817-08 | g.chr10:15885221C>A | c.225G>T | c.(223-225)cgG>cgT | p.R75R |
OV | 10 | 15838108 | 15838108 | + | Missense_Mutation | SNP | C | C | T | TCGA-23-2645-01A-01W-1091-09 | TCGA-23-2645-10A-01W-1091-09 | g.chr10:15838108C>T | c.946G>A | c.(946-948)Gac>Aac | p.D316N |
OV | 10 | 15876568 | 15876568 | + | Silent | SNP | C | C | T | TCGA-13-0793-01A-01W-0370-10 | TCGA-13-0793-10A-01W-0370-10 | g.chr10:15876568C>T | c.624G>A | c.(622-624)ttG>ttA | p.L208L |
PCPG | 10 | 15883458 | 15883458 | + | Missense_Mutation | SNP | G | G | A | TCGA-QR-A6H2-01A-11D-A35D-08 | TCGA-QR-A6H2-10A-01D-A35B-08 | g.chr10:15883458G>A | c.376C>T | c.(376-378)Cct>Tct | p.P126S |
PRAD | 10 | 15879270 | 15879270 | + | Missense_Mutation | SNP | T | T | C | TCGA-EJ-7794-01A-11D-2114-08 | TCGA-EJ-7794-10A-01D-2115-08 | g.chr10:15879270T>C | c.509A>G | c.(508-510)gAc>gGc | p.D170G |
READ | 10 | 15838104 | 15838104 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr10:15838104G>A | c.950C>T | c.(949-951)cCa>cTa | p.P317L |
SARC | 10 | 15902295 | 15902295 | + | Missense_Mutation | SNP | A | A | G | TCGA-DX-AB32-01A-11D-A417-09 | TCGA-DX-AB32-10A-01D-A41A-09 | g.chr10:15902295A>G | c.4T>C | c.(4-6)Tcc>Ccc | p.S2P |
SKCM | 10 | 15824206 | 15824206 | + | Missense_Mutation | SNP | G | G | A | TCGA-DA-A1HV-06A-21D-A196-08 | TCGA-DA-A1HV-10A-01D-A198-08 | g.chr10:15824206G>A | c.1136C>T | c.(1135-1137)tCt>tTt | p.S379F |
SKCM | 10 | 15828602 | 15828602 | + | Silent | SNP | G | G | A | TCGA-EE-A2GI-06A-11D-A196-08 | TCGA-EE-A2GI-10A-01D-A198-08 | g.chr10:15828602G>A | c.1074C>T | c.(1072-1074)atC>atT | p.I358I |
SKCM | 10 | 15828640 | 15828640 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr10:15828640G>A | c.1036C>T | c.(1036-1038)Ctc>Ttc | p.L346F |
SKCM | 10 | 15838110 | 15838110 | + | Missense_Mutation | SNP | T | T | A | TCGA-EE-A29L-06A-12D-A196-08 | TCGA-EE-A29L-10A-01D-A198-08 | g.chr10:15838110T>A | c.944A>T | c.(943-945)tAc>tTc | p.Y315F |
SKCM | 10 | 15858885 | 15858885 | + | Silent | SNP | G | G | A | TCGA-EE-A3J5-06A-11D-A20D-08 | TCGA-EE-A3J5-10A-01D-A20D-08 | g.chr10:15858885G>A | c.831C>T | c.(829-831)ttC>ttT | p.F277F |
SKCM | 10 | 15879309 | 15879309 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3AD-06A-11D-A196-08 | TCGA-EE-A3AD-10A-01D-A198-08 | g.chr10:15879309G>A | c.470C>T | c.(469-471)tCg>tTg | p.S157L |
SKCM | 10 | 15879309 | 15879309 | + | Missense_Mutation | SNP | G | G | A | TCGA-FS-A4F0-06A-11D-A24R-08 | TCGA-FS-A4F0-10A-01D-A24R-08 | g.chr10:15879309G>A | c.470C>T | c.(469-471)tCg>tTg | p.S157L |
SKCM | 10 | 15885240 | 15885240 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr10:15885240G>A | c.206C>T | c.(205-207)tCg>tTg | p.S69L |