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 | 15 | 63850344 | 63850344 | + | Missense_Mutation | SNP | T | T | G | TCGA-DK-A1AC-01A-11D-A13W-08 | TCGA-DK-A1AC-10A-01D-A13W-08 | g.chr15:63850344T>G | c.490T>G | c.(490-492)Ttg>Gtg | p.L164V |
BLCA | 15 | 63852116 | 63852116 | + | Silent | SNP | G | G | A | TCGA-4Z-AA84-01A-11D-A391-08 | TCGA-4Z-AA84-10A-01D-A394-08 | g.chr15:63852116G>A | c.594G>A | c.(592-594)ggG>ggA | p.G198G |
BLCA | 15 | 63855159 | 63855159 | + | Missense_Mutation | SNP | G | G | A | TCGA-GD-A76B-01A-11D-A32B-08 | TCGA-GD-A76B-10A-01D-A329-08 | g.chr15:63855159G>A | c.713G>A | c.(712-714)aGc>aAc | p.S238N |
BLCA | 15 | 63862666 | 63862666 | + | Missense_Mutation | SNP | C | C | T | TCGA-GU-A763-01A-11D-A32B-08 | TCGA-GU-A763-10A-01D-A329-08 | g.chr15:63862666C>T | c.796C>T | c.(796-798)Cgc>Tgc | p.R266C |
BLCA | 15 | 63880539 | 63880539 | + | Missense_Mutation | SNP | G | G | A | TCGA-UY-A9PE-01A-11D-A38G-08 | TCGA-UY-A9PE-10A-01D-A38J-08 | g.chr15:63880539G>A | c.1132G>A | c.(1132-1134)Gat>Aat | p.D378N |
BLCA | 15 | 63880542 | 63880547 | + | In_Frame_Del | DEL | GAGACA | GAGACA | - | TCGA-FJ-A871-01A-11D-A34U-08 | TCGA-FJ-A871-10A-01D-A34X-08 | g.chr15:63880542_63880547delGAGACA | c.1135_1140delGAGACA | c.(1135-1140)gagacadel | p.ET379del |
BLCA | 15 | 63880588 | 63880588 | + | Missense_Mutation | SNP | C | C | A | TCGA-G2-A2EL-01A-12D-A18F-08 | TCGA-G2-A2EL-10A-01D-A18F-08 | g.chr15:63880588C>A | c.1181C>A | c.(1180-1182)tCc>tAc | p.S394Y |
BLCA | 15 | 63882911 | 63882911 | + | Missense_Mutation | SNP | C | C | G | TCGA-ZF-AA51-01A-21D-A391-08 | TCGA-ZF-AA51-10A-01D-A394-08 | g.chr15:63882911C>G | c.1449C>G | c.(1447-1449)ttC>ttG | p.F483L |
BLCA | 15 | 63882938 | 63882938 | + | Silent | SNP | G | G | C | TCGA-GU-A767-01A-11D-A32B-08 | TCGA-GU-A767-10A-01D-A329-08 | g.chr15:63882938G>C | c.1476G>C | c.(1474-1476)ctG>ctC | p.L492L |
BRCA | 15 | 63866266 | 63866266 | + | Silent | SNP | C | C | T | TCGA-GI-A2C8-01A-11D-A16D-09 | TCGA-GI-A2C8-11A-22D-A16D-09 | g.chr15:63866266C>T | c.930C>T | c.(928-930)gtC>gtT | p.V310V |
BRCA | 15 | 63866545 | 63866545 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-GI-A2C8-01A-11D-A16D-09 | TCGA-GI-A2C8-11A-22D-A16D-09 | g.chr15:63866545C>T | c.1039C>T | c.(1039-1041)Cag>Tag | p.Q347* |
CESC | 15 | 63880981 | 63880981 | + | Silent | SNP | G | G | A | TCGA-Q1-A73P-01A-11D-A32I-09 | TCGA-Q1-A73P-10B-01D-A32I-09 | g.chr15:63880981G>A | c.1296G>A | c.(1294-1296)ctG>ctA | p.L432L |
COAD | 15 | 63862651 | 63862651 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3811-01A-01W-0995-10 | TCGA-AA-3811-10A-01W-0995-10 | g.chr15:63862651G>A | c.781G>A | c.(781-783)Gcc>Acc | p.A261T |
COAD | 15 | 63862684 | 63862684 | + | Missense_Mutation | SNP | C | C | A | TCGA-A6-2672-01A-01W-0833-10 | TCGA-A6-2672-10A-01W-0833-10 | g.chr15:63862684C>A | c.814C>A | c.(814-816)Cta>Ata | p.L272I |
COAD | 15 | 63866267 | 63866267 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3815-01A-01W-0995-10 | TCGA-AA-3815-10A-01W-0995-10 | g.chr15:63866267A>G | c.931A>G | c.(931-933)Acg>Gcg | p.T311A |
COAD | 15 | 63866324 | 63866324 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr15:63866324G>A | c.988G>A | c.(988-990)Gaa>Aaa | p.E330K |
COAD | 15 | 63880577 | 63880577 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr15:63880577G>T | c.1170G>T | c.(1168-1170)aaG>aaT | p.K390N |
COAD | 15 | 63880997 | 63880997 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr15:63880997A>G | c.1312A>G | c.(1312-1314)Aaa>Gaa | p.K438E |
COAD | 15 | 63881207 | 63881207 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3542-01A-02W-0831-10 | TCGA-AA-3542-10A-01W-0831-10 | g.chr15:63881207C>A | c.1394C>A | c.(1393-1395)tCc>tAc | p.S465Y |
COAD | 15 | 63882927 | 63882927 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr15:63882927A>G | c.1465A>G | c.(1465-1467)Act>Gct | p.T489A |
COADREAD | 15 | 63862651 | 63862651 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3811-01A-01W-0995-10 | TCGA-AA-3811-10A-01W-0995-10 | g.chr15:63862651G>A | c.781G>A | c.(781-783)Gcc>Acc | p.A261T |
COADREAD | 15 | 63862684 | 63862684 | + | Missense_Mutation | SNP | C | C | A | TCGA-A6-2672-01A-01W-0833-10 | TCGA-A6-2672-10A-01W-0833-10 | g.chr15:63862684C>A | c.814C>A | c.(814-816)Cta>Ata | p.L272I |
COADREAD | 15 | 63866267 | 63866267 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3815-01A-01W-0995-10 | TCGA-AA-3815-10A-01W-0995-10 | g.chr15:63866267A>G | c.931A>G | c.(931-933)Acg>Gcg | p.T311A |
COADREAD | 15 | 63866324 | 63866324 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr15:63866324G>A | c.988G>A | c.(988-990)Gaa>Aaa | p.E330K |
COADREAD | 15 | 63880577 | 63880577 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr15:63880577G>T | c.1170G>T | c.(1168-1170)aaG>aaT | p.K390N |
COADREAD | 15 | 63880997 | 63880997 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr15:63880997A>G | c.1312A>G | c.(1312-1314)Aaa>Gaa | p.K438E |
COADREAD | 15 | 63881207 | 63881207 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3542-01A-02W-0831-10 | TCGA-AA-3542-10A-01W-0831-10 | g.chr15:63881207C>A | c.1394C>A | c.(1393-1395)tCc>tAc | p.S465Y |
COADREAD | 15 | 63882927 | 63882927 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr15:63882927A>G | c.1465A>G | c.(1465-1467)Act>Gct | p.T489A |
DLBC | 15 | 63829314 | 63829314 | + | Missense_Mutation | SNP | G | G | T | TCGA-RQ-A68N-01A-11D-A31X-10 | TCGA-RQ-A68N-10A-01D-A31X-10 | g.chr15:63829314G>T | c.243G>T | c.(241-243)caG>caT | p.Q81H |
DLBC | 15 | 63855190 | 63855190 | + | Silent | SNP | G | G | A | TCGA-G8-6907-01A-11D-2210-10 | TCGA-G8-6907-14A-01D-2210-10 | g.chr15:63855190G>A | c.744G>A | c.(742-744)aaG>aaA | p.K248K |
ESCA | 15 | 63862741 | 63862741 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-Z6-A8JD-01A-11D-A36J-09 | TCGA-Z6-A8JD-10A-01D-A36M-09 | g.chr15:63862741G>T | c.871G>T | c.(871-873)Gag>Tag | p.E291* |
ESCA | 15 | 63866317 | 63866317 | + | Nonsense_Mutation | SNP | T | T | A | TCGA-2H-A9GG-01A-11D-A37C-09 | TCGA-2H-A9GG-11A-11D-A37F-09 | g.chr15:63866317T>A | c.981T>A | c.(979-981)tgT>tgA | p.C327* |
ESCA | 15 | 63866552 | 63866552 | + | Missense_Mutation | SNP | G | G | C | TCGA-LN-A4A9-01A-11D-A28B-09 | TCGA-LN-A4A9-10A-01D-A28E-09 | g.chr15:63866552G>C | c.1046G>C | c.(1045-1047)aGa>aCa | p.R349T |
GBMLGG | 15 | 63855167 | 63855167 | + | Missense_Mutation | SNP | T | T | C | TCGA-DB-A4XG-01A-11D-A27K-08 | TCGA-DB-A4XG-10A-01D-A27N-08 | g.chr15:63855167T>C | c.721T>C | c.(721-723)Tcc>Ccc | p.S241P |
GBMLGG | 15 | 63855173 | 63855173 | + | Missense_Mutation | SNP | T | T | G | TCGA-DH-A7UV-01A-12D-A34A-08 | TCGA-DH-A7UV-10A-01D-A34A-08 | g.chr15:63855173T>G | c.727T>G | c.(727-729)Ttt>Gtt | p.F243V |
GBMLGG | 15 | 63866561 | 63866561 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr15:63866561G>A | c.1055G>A | c.(1054-1056)cGc>cAc | p.R352H |
GBMLGG | 15 | 63880966 | 63880966 | + | Silent | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr15:63880966C>T | c.1281C>T | c.(1279-1281)taC>taT | p.Y427Y |
HNSC | 15 | 63866568 | 63866568 | + | Missense_Mutation | SNP | G | G | T | TCGA-BA-4077-01B-01D-1434-08 | TCGA-BA-4077-10A-01D-1434-08 | g.chr15:63866568G>T | c.1062G>T | c.(1060-1062)aaG>aaT | p.K354N |
HNSC | 15 | 63866570 | 63866570 | + | Missense_Mutation | SNP | A | A | T | TCGA-F7-A61W-01A-11D-A28R-08 | TCGA-F7-A61W-10A-01D-A28U-08 | g.chr15:63866570A>T | c.1064A>T | c.(1063-1065)aAt>aTt | p.N355I |
HNSC | 15 | 63881009 | 63881009 | + | Silent | SNP | C | C | T | TCGA-QK-A8Z9-01B-11D-A391-08 | TCGA-QK-A8Z9-10A-01D-A394-08 | g.chr15:63881009C>T | c.1324C>T | c.(1324-1326)Cta>Tta | p.L442L |
HNSC | 15 | 63882861 | 63882861 | + | Splice_Site | SNP | G | G | A | TCGA-UF-A71D-01A-12D-A34J-08 | TCGA-UF-A71D-10B-01D-A34M-08 | g.chr15:63882861G>A | c.1399G>A | c.(1399-1401)Gtt>Att | p.V467I |
HNSC | 15 | 63883006 | 63883006 | + | Missense_Mutation | SNP | C | C | G | TCGA-CQ-7071-01A-12D-A30E-08 | TCGA-CQ-7071-10A-01D-A30H-08 | g.chr15:63883006C>G | c.1544C>G | c.(1543-1545)gCt>gGt | p.A515G |
KICH | 15 | 63866525 | 63866525 | + | Missense_Mutation | SNP | T | T | C | TCGA-KL-8328-01A-11D-2310-10 | TCGA-KL-8328-11A-01D-2310-10 | g.chr15:63866525T>C | c.1019T>C | c.(1018-1020)cTt>cCt | p.L340P |
KIPAN | 15 | 63866525 | 63866525 | + | Missense_Mutation | SNP | T | T | C | TCGA-KL-8328-01A-11D-2310-10 | TCGA-KL-8328-11A-01D-2310-10 | g.chr15:63866525T>C | c.1019T>C | c.(1018-1020)cTt>cCt | p.L340P |
KIPAN | 15 | 63866572 | 63866572 | + | Missense_Mutation | SNP | C | C | A | TCGA-IA-A83S-01A-11D-A34Z-10 | TCGA-IA-A83S-11A-11D-A34Z-10 | g.chr15:63866572C>A | c.1066C>A | c.(1066-1068)Caa>Aaa | p.Q356K |
KIPAN | 15 | 63882867 | 63882867 | + | Missense_Mutation | SNP | T | T | G | TCGA-AL-3468-01A-01D-1252-08 | TCGA-AL-3468-10A-01D-1252-08 | g.chr15:63882867T>G | c.1405T>G | c.(1405-1407)Tct>Gct | p.S469A |
KIRP | 15 | 63866572 | 63866572 | + | Missense_Mutation | SNP | C | C | A | TCGA-IA-A83S-01A-11D-A34Z-10 | TCGA-IA-A83S-11A-11D-A34Z-10 | g.chr15:63866572C>A | c.1066C>A | c.(1066-1068)Caa>Aaa | p.Q356K |
KIRP | 15 | 63882867 | 63882867 | + | Missense_Mutation | SNP | T | T | G | TCGA-AL-3468-01A-01D-1252-08 | TCGA-AL-3468-10A-01D-1252-08 | g.chr15:63882867T>G | c.1405T>G | c.(1405-1407)Tct>Gct | p.S469A |
LGG | 15 | 63855167 | 63855167 | + | Missense_Mutation | SNP | T | T | C | TCGA-DB-A4XG-01A-11D-A27K-08 | TCGA-DB-A4XG-10A-01D-A27N-08 | g.chr15:63855167T>C | c.721T>C | c.(721-723)Tcc>Ccc | p.S241P |
LGG | 15 | 63855173 | 63855173 | + | Missense_Mutation | SNP | T | T | G | TCGA-DH-A7UV-01A-12D-A34A-08 | TCGA-DH-A7UV-10A-01D-A34A-08 | g.chr15:63855173T>G | c.727T>G | c.(727-729)Ttt>Gtt | p.F243V |
LGG | 15 | 63866561 | 63866561 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr15:63866561G>A | c.1055G>A | c.(1054-1056)cGc>cAc | p.R352H |
LGG | 15 | 63880966 | 63880966 | + | Silent | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr15:63880966C>T | c.1281C>T | c.(1279-1281)taC>taT | p.Y427Y |
LIHC | 15 | 63850378 | 63850378 | + | Missense_Mutation | SNP | A | A | G | TCGA-ES-A2HT-01A-12D-A183-10 | TCGA-ES-A2HT-11A-11D-A183-10 | g.chr15:63850378A>G | c.524A>G | c.(523-525)cAg>cGg | p.Q175R |
LIHC | 15 | 63881201 | 63881201 | + | Missense_Mutation | SNP | A | A | G | TCGA-DD-AAEB-01A-11D-A40R-10 | TCGA-DD-AAEB-10A-01D-A40U-10 | g.chr15:63881201A>G | c.1388A>G | c.(1387-1389)cAt>cGt | p.H463R |
LUAD | 15 | 63829318 | 63829318 | + | Missense_Mutation | SNP | A | A | C | TCGA-35-4122-01A-01D-1105-08 | TCGA-35-4122-10A-01D-1105-08 | g.chr15:63829318A>C | c.247A>C | c.(247-249)Aca>Cca | p.T83P |
LUAD | 15 | 63862705 | 63862705 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-78-7155-01A-11D-2036-08 | TCGA-78-7155-10A-01D-2036-08 | g.chr15:63862705delG | c.835delG | c.(835-837)ggtfs | p.G279fs |
LUSC | 15 | 63883009 | 63883009 | + | Missense_Mutation | SNP | G | G | A | TCGA-56-1622-01A-01D-1521-08 | TCGA-56-1622-11A-01D-1521-08 | g.chr15:63883009G>A | c.1547G>A | c.(1546-1548)gGa>gAa | p.G516E |
PRAD | 15 | 63824850 | 63824850 | + | Silent | SNP | C | C | T | TCGA-EJ-AB20-01A-12D-A41K-08 | TCGA-EJ-AB20-10A-01D-A41N-08 | g.chr15:63824850C>T | c.96C>T | c.(94-96)tgC>tgT | p.C32C |
PRAD | 15 | 63852135 | 63852135 | + | Missense_Mutation | SNP | A | A | G | TCGA-G9-6339-01A-12D-A30X-08 | TCGA-G9-6339-10A-01D-A30X-08 | g.chr15:63852135A>G | c.613A>G | c.(613-615)Aca>Gca | p.T205A |
SKCM | 15 | 63850313 | 63850313 | + | Silent | SNP | C | C | T | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr15:63850313C>T | c.459C>T | c.(457-459)acC>acT | p.T153T |
SKCM | 15 | 63855103 | 63855103 | + | Silent | SNP | A | A | G | TCGA-RP-A693-06A-13D-A30X-08 | TCGA-RP-A693-10A-01D-A30X-08 | g.chr15:63855103A>G | c.657A>G | c.(655-657)gtA>gtG | p.V219V |
SKCM | 15 | 63855104 | 63855104 | + | Missense_Mutation | SNP | G | G | A | TCGA-RP-A693-06A-13D-A30X-08 | TCGA-RP-A693-10A-01D-A30X-08 | g.chr15:63855104G>A | c.658G>A | c.(658-660)Gaa>Aaa | p.E220K |