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 | 9 | 123526953 | 123526953 | + | Missense_Mutation | SNP | C | C | T | TCGA-DK-A6B1-01A-12D-A30E-08 | TCGA-DK-A6B1-10A-01D-A30H-08 | g.chr9:123526953C>T | c.1249G>A | c.(1249-1251)Gca>Aca | p.A417T |
BLCA | 9 | 123526972 | 123526972 | + | Missense_Mutation | SNP | C | C | G | TCGA-FD-A43P-01A-31D-A23U-08 | TCGA-FD-A43P-10A-01D-A23U-08 | g.chr9:123526972C>G | c.1230G>C | c.(1228-1230)aaG>aaC | p.K410N |
BLCA | 9 | 123527035 | 123527035 | + | Silent | SNP | G | G | A | TCGA-FD-A6TC-01A-21D-A339-08 | TCGA-FD-A6TC-10A-21D-A339-08 | g.chr9:123527035G>A | c.1167C>T | c.(1165-1167)atC>atT | p.I389I |
BLCA | 9 | 123540762 | 123540762 | + | Silent | SNP | G | G | A | TCGA-XF-AAN0-01A-11D-A42E-08 | TCGA-XF-AAN0-10A-01D-A42H-08 | g.chr9:123540762G>A | c.552C>T | c.(550-552)atC>atT | p.I184I |
BLCA | 9 | 123550224 | 123550224 | + | Missense_Mutation | SNP | A | A | C | TCGA-DK-A6AW-01A-11D-A30E-08 | TCGA-DK-A6AW-10A-01D-A30H-08 | g.chr9:123550224A>C | c.313T>G | c.(313-315)Ttg>Gtg | p.L105V |
BLCA | 9 | 123550366 | 123550366 | + | Silent | SNP | G | G | C | TCGA-BT-A3PH-01A-11D-A21Z-08 | TCGA-BT-A3PH-10A-01D-A21Z-08 | g.chr9:123550366G>C | c.171C>G | c.(169-171)ctC>ctG | p.L57L |
BLCA | 9 | 123550458 | 123550458 | + | Missense_Mutation | SNP | C | C | T | TCGA-DK-AA6Q-01A-11D-A391-08 | TCGA-DK-AA6Q-10A-01D-A394-08 | g.chr9:123550458C>T | c.79G>A | c.(79-81)Gaa>Aaa | p.E27K |
BLCA | 9 | 123550531 | 123550531 | + | Missense_Mutation | SNP | C | C | G | TCGA-DK-AA6Q-01A-11D-A391-08 | TCGA-DK-AA6Q-10A-01D-A394-08 | g.chr9:123550531C>G | c.6G>C | c.(4-6)gaG>gaC | p.E2D |
BRCA | 9 | 123526846 | 123526846 | + | Silent | SNP | C | C | T | TCGA-BH-A0HF-01A-11W-A071-09 | TCGA-BH-A0HF-10A-01W-A071-09 | g.chr9:123526846C>T | c.1356G>A | c.(1354-1356)gaG>gaA | p.E452E |
BRCA | 9 | 123527011 | 123527011 | + | Silent | SNP | C | C | G | TCGA-AC-A23H-01A-11D-A159-09 | TCGA-AC-A23H-11A-12D-A17G-09 | g.chr9:123527011C>G | c.1191G>C | c.(1189-1191)ctG>ctC | p.L397L |
BRCA | 9 | 123527031 | 123527031 | + | Missense_Mutation | SNP | C | C | T | TCGA-D8-A27G-01A-11D-A16D-09 | TCGA-D8-A27G-10A-01D-A16D-09 | g.chr9:123527031C>T | c.1171G>A | c.(1171-1173)Gac>Aac | p.D391N |
BRCA | 9 | 123533674 | 123533674 | + | Missense_Mutation | SNP | G | G | A | TCGA-A2-A0EY-01A-11W-A050-09 | TCGA-A2-A0EY-10A-01W-A055-09 | g.chr9:123533674G>A | c.1028C>T | c.(1027-1029)tCa>tTa | p.S343L |
BRCA | 9 | 123535049 | 123535049 | + | Missense_Mutation | SNP | C | C | T | TCGA-D8-A27G-01A-11D-A16D-09 | TCGA-D8-A27G-10A-01D-A16D-09 | g.chr9:123535049C>T | c.889G>A | c.(889-891)Gac>Aac | p.D297N |
BRCA | 9 | 123550286 | 123550286 | + | Missense_Mutation | SNP | G | G | C | TCGA-E2-A15M-01A-11D-A12B-09 | TCGA-E2-A15M-11A-22D-A12B-09 | g.chr9:123550286G>C | c.251C>G | c.(250-252)tCt>tGt | p.S84C |
CESC | 9 | 123533705 | 123533705 | + | Missense_Mutation | SNP | G | G | A | TCGA-DR-A0ZM-01A-12D-A10S-08 | TCGA-DR-A0ZM-10A-01D-A10S-08 | g.chr9:123533705G>A | c.997C>T | c.(997-999)Cat>Tat | p.H333Y |
CESC | 9 | 123540630 | 123540630 | + | Splice_Site | SNP | C | C | T | TCGA-EK-A2PI-01A-11D-A18J-09 | TCGA-EK-A2PI-10A-01D-A18J-09 | g.chr9:123540630C>T | c.684G>A | c.(682-684)gcG>gcA | p.A228A |
CHOL | 9 | 123550286 | 123550286 | + | Missense_Mutation | SNP | G | G | T | TCGA-4G-AAZO-01A-12D-A417-09 | TCGA-4G-AAZO-11A-11D-A41A-09 | g.chr9:123550286G>T | c.251C>A | c.(250-252)tCt>tAt | p.S84Y |
COAD | 9 | 123527004 | 123527004 | + | Missense_Mutation | SNP | G | G | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr9:123527004G>A | c.1198C>T | c.(1198-1200)Cgc>Tgc | p.R400C |
COAD | 9 | 123538407 | 123538407 | + | Silent | SNP | C | C | A | TCGA-A6-5661-01A-01D-1650-10 | TCGA-A6-5661-10A-01D-1650-10 | g.chr9:123538407C>A | c.783G>T | c.(781-783)ctG>ctT | p.L261L |
COAD | 9 | 123538408 | 123538408 | + | Missense_Mutation | SNP | A | A | G | TCGA-D5-6533-01A-11D-1719-10 | TCGA-D5-6533-10A-01D-1719-10 | g.chr9:123538408A>G | c.782T>C | c.(781-783)cTg>cCg | p.L261P |
COAD | 9 | 123538451 | 123538451 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr9:123538451C>A | c.739G>T | c.(739-741)Gac>Tac | p.D247Y |
COAD | 9 | 123550475 | 123550475 | + | Missense_Mutation | SNP | G | G | A | TCGA-CM-4743-01A-01D-1719-10 | TCGA-CM-4743-10A-01D-1719-10 | g.chr9:123550475G>A | c.62C>T | c.(61-63)aCg>aTg | p.T21M |
COAD | 9 | 123550529 | 123550529 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr9:123550529C>A | c.8G>T | c.(7-9)aGa>aTa | p.R3I |
COADREAD | 9 | 123527004 | 123527004 | + | Missense_Mutation | SNP | G | G | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr9:123527004G>A | c.1198C>T | c.(1198-1200)Cgc>Tgc | p.R400C |
COADREAD | 9 | 123538407 | 123538407 | + | Silent | SNP | C | C | A | TCGA-A6-5661-01A-01D-1650-10 | TCGA-A6-5661-10A-01D-1650-10 | g.chr9:123538407C>A | c.783G>T | c.(781-783)ctG>ctT | p.L261L |
COADREAD | 9 | 123538408 | 123538408 | + | Missense_Mutation | SNP | A | A | G | TCGA-D5-6533-01A-11D-1719-10 | TCGA-D5-6533-10A-01D-1719-10 | g.chr9:123538408A>G | c.782T>C | c.(781-783)cTg>cCg | p.L261P |
COADREAD | 9 | 123538451 | 123538451 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr9:123538451C>A | c.739G>T | c.(739-741)Gac>Tac | p.D247Y |
COADREAD | 9 | 123550147 | 123550147 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-3892-01A-01W-1073-09 | TCGA-AG-3892-10A-01W-1073-09 | g.chr9:123550147C>A | c.390G>T | c.(388-390)atG>atT | p.M130I |
COADREAD | 9 | 123550475 | 123550475 | + | Missense_Mutation | SNP | G | G | A | TCGA-CM-4743-01A-01D-1719-10 | TCGA-CM-4743-10A-01D-1719-10 | g.chr9:123550475G>A | c.62C>T | c.(61-63)aCg>aTg | p.T21M |
COADREAD | 9 | 123550529 | 123550529 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr9:123550529C>A | c.8G>T | c.(7-9)aGa>aTa | p.R3I |
ESCA | 9 | 123527004 | 123527004 | + | Missense_Mutation | SNP | G | G | T | TCGA-L5-A4OJ-01A-11D-A27G-09 | TCGA-L5-A4OJ-11A-12D-A27G-09 | g.chr9:123527004G>T | c.1198C>A | c.(1198-1200)Cgc>Agc | p.R400S |
ESCA | 9 | 123538400 | 123538400 | + | Missense_Mutation | SNP | G | G | T | TCGA-LN-A8I1-01A-11D-A36J-09 | TCGA-LN-A8I1-10A-01D-A36M-09 | g.chr9:123538400G>T | c.790C>A | c.(790-792)Ctc>Atc | p.L264I |
ESCA | 9 | 123550234 | 123550234 | + | Silent | SNP | T | T | C | TCGA-L5-A8NM-01A-11D-A37C-09 | TCGA-L5-A8NM-11A-12D-A37F-09 | g.chr9:123550234T>C | c.303A>G | c.(301-303)gcA>gcG | p.A101A |
HNSC | 9 | 123538450 | 123538450 | + | Missense_Mutation | SNP | T | T | A | TCGA-IQ-A61L-01A-11D-A30E-08 | TCGA-IQ-A61L-10A-01D-A30H-08 | g.chr9:123538450T>A | c.740A>T | c.(739-741)gAc>gTc | p.D247V |
HNSC | 9 | 123540631 | 123540631 | + | Missense_Mutation | SNP | G | G | A | TCGA-HD-A633-01A-11D-A28R-08 | TCGA-HD-A633-10A-01D-A28U-08 | g.chr9:123540631G>A | c.683C>T | c.(682-684)gCg>gTg | p.A228V |
HNSC | 9 | 123550177 | 123550177 | + | Silent | SNP | C | C | T | TCGA-CR-7398-01A-11D-2012-08 | TCGA-CR-7398-10A-01D-2013-08 | g.chr9:123550177C>T | c.360G>A | c.(358-360)aaG>aaA | p.K120K |
KIPAN | 9 | 123527053 | 123527053 | + | Silent | SNP | G | G | A | TCGA-A4-8312-01A-11D-2396-08 | TCGA-A4-8312-10A-01D-2396-08 | g.chr9:123527053G>A | c.1149C>T | c.(1147-1149)gaC>gaT | p.D383D |
KIPAN | 9 | 123533652 | 123533652 | + | Missense_Mutation | SNP | C | C | G | TCGA-2Z-A9JE-01A-11D-A42J-10 | TCGA-2Z-A9JE-10A-01D-A42M-10 | g.chr9:123533652C>G | c.1050G>C | c.(1048-1050)tgG>tgC | p.W350C |
KIRP | 9 | 123527053 | 123527053 | + | Silent | SNP | G | G | A | TCGA-A4-8312-01A-11D-2396-08 | TCGA-A4-8312-10A-01D-2396-08 | g.chr9:123527053G>A | c.1149C>T | c.(1147-1149)gaC>gaT | p.D383D |
KIRP | 9 | 123533652 | 123533652 | + | Missense_Mutation | SNP | C | C | G | TCGA-2Z-A9JE-01A-11D-A42J-10 | TCGA-2Z-A9JE-10A-01D-A42M-10 | g.chr9:123533652C>G | c.1050G>C | c.(1048-1050)tgG>tgC | p.W350C |
LIHC | 9 | 123526906 | 123526906 | + | Silent | SNP | C | C | T | TCGA-DD-A3A9-01A-11D-A25V-10 | TCGA-DD-A3A9-11A-11D-A25V-10 | g.chr9:123526906C>T | c.1296G>A | c.(1294-1296)acG>acA | p.T432T |
LIHC | 9 | 123526947 | 123526947 | + | Missense_Mutation | SNP | C | C | T | TCGA-EP-A2KA-01A-11D-A183-10 | TCGA-EP-A2KA-10A-01D-A183-10 | g.chr9:123526947C>T | c.1255G>A | c.(1255-1257)Gaa>Aaa | p.E419K |
LIHC | 9 | 123526956 | 123526956 | + | Missense_Mutation | SNP | G | G | T | TCGA-EP-A2KA-01A-11D-A183-10 | TCGA-EP-A2KA-10A-01D-A183-10 | g.chr9:123526956G>T | c.1246C>A | c.(1246-1248)Ctg>Atg | p.L416M |
LIHC | 9 | 123533666 | 123533666 | + | Missense_Mutation | SNP | C | C | T | TCGA-4R-AA8I-01A-11D-A382-10 | TCGA-4R-AA8I-10B-01D-A385-10 | g.chr9:123533666C>T | c.1036G>A | c.(1036-1038)Ggt>Agt | p.G346S |
LUAD | 9 | 123535119 | 123535119 | + | Splice_Site | SNP | C | C | A | TCGA-64-5781-01A-01D-1625-08 | TCGA-64-5781-10A-01D-1625-08 | g.chr9:123535119C>A | | c.e6-1 | |
LUAD | 9 | 123538385 | 123538385 | + | Missense_Mutation | SNP | C | C | T | TCGA-86-A4JF-01A-11D-A24P-08 | TCGA-86-A4JF-10A-01D-A24P-08 | g.chr9:123538385C>T | c.805G>A | c.(805-807)Gaa>Aaa | p.E269K |
LUAD | 9 | 123538418 | 123538418 | + | Missense_Mutation | SNP | C | C | A | TCGA-55-7994-01A-11D-2184-08 | TCGA-55-7994-10A-01D-2184-08 | g.chr9:123538418C>A | c.772G>T | c.(772-774)Ggg>Tgg | p.G258W |
LUAD | 9 | 123550109 | 123550109 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-17-Z031-01A-01W-0746-08 | TCGA-17-Z031-11A-01W-0746-08 | g.chr9:123550109G>C | c.428C>G | c.(427-429)tCa>tGa | p.S143* |
OV | 9 | 123538409 | 123538409 | + | Missense_Mutation | SNP | G | G | C | TCGA-04-1530-01A-02W-0552-10 | TCGA-04-1530-10A-01W-0552-10 | g.chr9:123538409G>C | c.781C>G | c.(781-783)Ctg>Gtg | p.L261V |
PAAD | 9 | 123527025 | 123527025 | + | Missense_Mutation | SNP | G | G | A | TCGA-HV-A7OL-01A-11D-A33T-08 | TCGA-HV-A7OL-10A-01D-A33W-08 | g.chr9:123527025G>A | c.1177C>T | c.(1177-1179)Cgg>Tgg | p.R393W |
PAAD | 9 | 123527025 | 123527025 | + | Missense_Mutation | SNP | G | G | A | TCGA-US-A77J-01A-11D-A32N-08 | TCGA-US-A77J-11A-11D-A32N-08 | g.chr9:123527025G>A | c.1177C>T | c.(1177-1179)Cgg>Tgg | p.R393W |
PAAD | 9 | 123538497 | 123538497 | + | Silent | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr9:123538497G>A | c.693C>T | c.(691-693)agC>agT | p.S231S |
PCPG | 9 | 123550425 | 123550425 | + | Missense_Mutation | SNP | C | C | T | TCGA-RW-A68A-01A-11D-A35D-08 | TCGA-RW-A68A-11A-21D-A35B-08 | g.chr9:123550425C>T | c.112G>A | c.(112-114)Gca>Aca | p.A38T |
READ | 9 | 123550147 | 123550147 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-3892-01A-01W-1073-09 | TCGA-AG-3892-10A-01W-1073-09 | g.chr9:123550147C>A | c.390G>T | c.(388-390)atG>atT | p.M130I |
SKCM | 9 | 123550194 | 123550194 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A2JF-06A-11D-A196-08 | TCGA-D3-A2JF-10A-01D-A198-08 | g.chr9:123550194C>T | c.343G>A | c.(343-345)Gac>Aac | p.D115N |
SKCM | 9 | 123550195 | 123550195 | + | Silent | SNP | C | C | T | TCGA-D3-A2JF-06A-11D-A196-08 | TCGA-D3-A2JF-10A-01D-A198-08 | g.chr9:123550195C>T | c.342G>A | c.(340-342)caG>caA | p.Q114Q |
SKCM | 9 | 123550268 | 123550268 | + | Missense_Mutation | SNP | A | A | C | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr9:123550268A>C | c.269T>G | c.(268-270)gTg>gGg | p.V90G |