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 |
ACC | 3 | 47036641 | 47036641 | + | Silent | SNP | G | G | A | TCGA-OR-A5J5-01A-11D-A29I-10 | TCGA-OR-A5J5-10A-01D-A29L-10 | g.chr3:47036641G>A | c.1416G>A | c.(1414-1416)gcG>gcA | p.A472A |
ACC | 3 | 47036675 | 47036675 | + | Missense_Mutation | SNP | G | G | T | TCGA-OR-A5L9-01A-11D-A29I-10 | TCGA-OR-A5L9-10B-01D-A29L-10 | g.chr3:47036675G>T | c.1450G>T | c.(1450-1452)Gcc>Tcc | p.A484S |
ACC | 3 | 47041809 | 47041809 | + | Missense_Mutation | SNP | C | C | A | TCGA-PK-A5HB-01A-11D-A29I-10 | TCGA-PK-A5HB-11A-11D-A29L-10 | g.chr3:47041809C>A | c.4220C>A | c.(4219-4221)tCc>tAc | p.S1407Y |
ACC | 3 | 47043602 | 47043602 | + | Missense_Mutation | SNP | G | G | A | TCGA-PA-A5YG-01A-11D-A29I-10 | TCGA-PA-A5YG-10A-01D-A29L-10 | g.chr3:47043602G>A | c.4975G>A | c.(4975-4977)Gag>Aag | p.E1659K |
BLCA | 3 | 47031020 | 47031020 | + | Missense_Mutation | SNP | G | G | A | TCGA-KQ-A41O-01A-12D-A34U-08 | TCGA-KQ-A41O-10D-01D-A34X-08 | g.chr3:47031020G>A | c.493G>A | c.(493-495)Gag>Aag | p.E165K |
BLCA | 3 | 47033343 | 47033343 | + | Missense_Mutation | SNP | G | G | A | TCGA-DK-A6B6-01A-11D-A30E-08 | TCGA-DK-A6B6-10A-01D-A30H-08 | g.chr3:47033343G>A | c.939G>A | c.(937-939)atG>atA | p.M313I |
BLCA | 3 | 47036911 | 47036911 | + | Silent | SNP | C | C | T | TCGA-KQ-A41S-01A-12D-A339-08 | TCGA-KQ-A41S-10C-01D-A339-08 | g.chr3:47036911C>T | c.1686C>T | c.(1684-1686)atC>atT | p.I562I |
BLCA | 3 | 47037250 | 47037250 | + | Missense_Mutation | SNP | G | G | A | TCGA-ZF-AA4W-01A-12D-A38G-08 | TCGA-ZF-AA4W-10A-01D-A38J-08 | g.chr3:47037250G>A | c.1945G>A | c.(1945-1947)Gcc>Acc | p.A649T |
BLCA | 3 | 47040207 | 47040207 | + | Splice_Site | SNP | C | C | T | TCGA-ZF-A9RC-01A-11D-A38G-08 | TCGA-ZF-A9RC-10A-01D-A38J-08 | g.chr3:47040207C>T | c.3222C>T | c.(3220-3222)agC>agT | p.S1074S |
BLCA | 3 | 47040469 | 47040469 | + | Silent | SNP | G | G | A | TCGA-FJ-A3ZF-01A-11D-A23M-08 | TCGA-FJ-A3ZF-10A-01D-A23K-08 | g.chr3:47040469G>A | c.3405G>A | c.(3403-3405)ctG>ctA | p.L1135L |
BLCA | 3 | 47044008 | 47044008 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-KQ-A41O-01A-12D-A34U-08 | TCGA-KQ-A41O-10D-01D-A34X-08 | g.chr3:47044008C>T | c.5299C>T | c.(5299-5301)Cag>Tag | p.Q1767* |
BLCA | 3 | 47044731 | 47044731 | + | Silent | SNP | G | G | A | TCGA-DK-A1A3-01A-11D-A13W-08 | TCGA-DK-A1A3-10A-01D-A13W-08 | g.chr3:47044731G>A | c.5652G>A | c.(5650-5652)gtG>gtA | p.V1884V |
BLCA | 3 | 47045403 | 47045403 | + | Missense_Mutation | SNP | G | G | A | TCGA-UY-A9PH-01A-11D-A38G-08 | TCGA-UY-A9PH-10A-01D-A38J-08 | g.chr3:47045403G>A | c.5818G>A | c.(5818-5820)Gag>Aag | p.E1940K |
BLCA | 3 | 47045451 | 47045451 | + | Missense_Mutation | SNP | G | G | A | TCGA-KQ-A41O-01A-12D-A34U-08 | TCGA-KQ-A41O-10D-01D-A34X-08 | g.chr3:47045451G>A | c.5866G>A | c.(5866-5868)Gtg>Atg | p.V1956M |
BLCA | 3 | 47045650 | 47045650 | + | Missense_Mutation | SNP | G | G | C | TCGA-UY-A9PH-01A-11D-A38G-08 | TCGA-UY-A9PH-10A-01D-A38J-08 | g.chr3:47045650G>C | c.5965G>C | c.(5965-5967)Gag>Cag | p.E1989Q |
BLCA | 3 | 47045991 | 47045991 | + | Missense_Mutation | SNP | G | G | A | TCGA-GD-A6C6-01A-21D-A31L-08 | TCGA-GD-A6C6-10A-01D-A31J-08 | g.chr3:47045991G>A | c.6205G>A | c.(6205-6207)Gta>Ata | p.V2069I |
BLCA | 3 | 47047473 | 47047473 | + | Missense_Mutation | SNP | T | T | C | TCGA-E7-A541-01A-11D-A26M-08 | TCGA-E7-A541-10A-01D-A26K-08 | g.chr3:47047473T>C | c.6839T>C | c.(6838-6840)aTc>aCc | p.I2280T |
BLCA | 3 | 47049918 | 47049918 | + | Missense_Mutation | SNP | G | G | A | TCGA-XF-AAMZ-01A-11D-A42E-08 | TCGA-XF-AAMZ-10A-01D-A42H-08 | g.chr3:47049918G>A | c.7865G>A | c.(7864-7866)cGt>cAt | p.R2622H |
BLCA | 3 | 47050035 | 47050035 | + | Missense_Mutation | SNP | C | C | T | TCGA-2F-A9KO-01A-11D-A38G-08 | TCGA-2F-A9KO-11A-12D-A38J-08 | g.chr3:47050035C>T | c.7904C>T | c.(7903-7905)tCa>tTa | p.S2635L |
BRCA | 3 | 47033996 | 47033996 | + | Missense_Mutation | SNP | G | G | C | TCGA-A8-A07C-01A-11D-A045-09 | TCGA-A8-A07C-10A-01W-A055-09 | g.chr3:47033996G>C | c.1064G>C | c.(1063-1065)gGg>gCg | p.G355A |
BRCA | 3 | 47036011 | 47036011 | + | Missense_Mutation | SNP | A | A | C | TCGA-A2-A0T5-01A-21D-A099-09 | TCGA-A2-A0T5-10A-01D-A099-09 | g.chr3:47036011A>C | c.1264A>C | c.(1264-1266)Acc>Ccc | p.T422P |
BRCA | 3 | 47037780 | 47037780 | + | Missense_Mutation | SNP | T | T | C | TCGA-E2-A1LA-01A-11D-A142-09 | TCGA-E2-A1LA-10A-01D-A142-09 | g.chr3:47037780T>C | c.2171T>C | c.(2170-2172)aTc>aCc | p.I724T |
BRCA | 3 | 47038822 | 47038822 | + | Missense_Mutation | SNP | A | A | G | TCGA-C8-A26Y-01A-11D-A16D-09 | TCGA-C8-A26Y-10A-01D-A16D-09 | g.chr3:47038822A>G | c.2723A>G | c.(2722-2724)gAg>gGg | p.E908G |
BRCA | 3 | 47041682 | 47041682 | + | Missense_Mutation | SNP | G | G | C | TCGA-A8-A08F-01A-11W-A019-09 | TCGA-A8-A08F-10A-01W-A021-09 | g.chr3:47041682G>C | c.4093G>C | c.(4093-4095)Gta>Cta | p.V1365L |
BRCA | 3 | 47043228 | 47043228 | + | Missense_Mutation | SNP | A | A | C | TCGA-A2-A0T5-01A-21D-A099-09 | TCGA-A2-A0T5-10A-01D-A099-09 | g.chr3:47043228A>C | c.4694A>C | c.(4693-4695)cAc>cCc | p.H1565P |
BRCA | 3 | 47045357 | 47045357 | + | Silent | SNP | C | C | T | TCGA-A8-A097-01A-11W-A050-09 | TCGA-A8-A097-10A-01D-A047-09 | g.chr3:47045357C>T | c.5772C>T | c.(5770-5772)gcC>gcT | p.A1924A |
BRCA | 3 | 47045770 | 47045770 | + | Missense_Mutation | SNP | A | A | C | TCGA-A8-A0A6-01A-12W-A071-09 | TCGA-A8-A0A6-10A-01W-A071-09 | g.chr3:47045770A>C | c.6085A>C | c.(6085-6087)Acc>Ccc | p.T2029P |
BRCA | 3 | 47045824 | 47045824 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-EW-A1PB-01A-11D-A142-09 | TCGA-EW-A1PB-10A-01D-A142-09 | g.chr3:47045824C>T | c.6139C>T | c.(6139-6141)Caa>Taa | p.Q2047* |
BRCA | 3 | 47045885 | 47045885 | + | Splice_Site | SNP | T | T | G | TCGA-A2-A0T6-01A-11D-A099-09 | TCGA-A2-A0T6-10A-01D-A099-09 | g.chr3:47045885T>G | | c.e37+2 | |
BRCA | 3 | 47047285 | 47047285 | + | Missense_Mutation | SNP | C | C | A | TCGA-BH-A0W7-01A-11D-A10Y-09 | TCGA-BH-A0W7-10A-01D-A110-09 | g.chr3:47047285C>A | c.6749C>A | c.(6748-6750)cCc>cAc | p.P2250H |
BRCA | 3 | 47047309 | 47047310 | + | Frame_Shift_Ins | INS | - | - | G | TCGA-A8-A086-01A-11W-A019-09 | TCGA-A8-A086-10A-01W-A021-09 | g.chr3:47047309_47047310insG | c.6773_6774insG | c.(6772-6777)gacttcfs | p.DF2258fs |
BRCA | 3 | 47049023 | 47049023 | + | Missense_Mutation | SNP | G | G | A | TCGA-AC-A3W7-01A-11D-A228-09 | TCGA-AC-A3W7-10A-01D-A22A-09 | g.chr3:47049023G>A | c.7343G>A | c.(7342-7344)cGa>cAa | p.R2448Q |
CESC | 3 | 47030778 | 47030778 | + | Missense_Mutation | SNP | G | G | A | TCGA-EK-A2RK-01A-11D-A18J-09 | TCGA-EK-A2RK-10A-01D-A18J-09 | g.chr3:47030778G>A | c.380G>A | c.(379-381)cGa>cAa | p.R127Q |
CESC | 3 | 47033349 | 47033349 | + | Silent | SNP | G | G | T | TCGA-Q1-A73O-01A-11D-A32I-09 | TCGA-Q1-A73O-10B-01D-A32I-09 | g.chr3:47033349G>T | c.945G>T | c.(943-945)ctG>ctT | p.L315L |
CESC | 3 | 47037080 | 47037080 | + | Missense_Mutation | SNP | A | A | G | TCGA-C5-A7CG-01A-11D-A32I-09 | TCGA-C5-A7CG-10A-01D-A32I-09 | g.chr3:47037080A>G | c.1855A>G | c.(1855-1857)Acc>Gcc | p.T619A |
CESC | 3 | 47039707 | 47039707 | + | Missense_Mutation | SNP | G | G | T | TCGA-EK-A2PL-01A-11D-A18J-09 | TCGA-EK-A2PL-10A-01D-A18J-09 | g.chr3:47039707G>T | c.3109G>T | c.(3109-3111)Gtg>Ttg | p.V1037L |
CESC | 3 | 47041727 | 47041727 | + | Missense_Mutation | SNP | C | C | G | TCGA-EK-A2H1-01A-11D-A17W-09 | TCGA-EK-A2H1-10A-01D-A17W-09 | g.chr3:47041727C>G | c.4138C>G | c.(4138-4140)Ctt>Gtt | p.L1380V |
CESC | 3 | 47042572 | 47042572 | + | Missense_Mutation | SNP | G | G | A | TCGA-DR-A0ZM-01A-12D-A10S-08 | TCGA-DR-A0ZM-10A-01D-A10S-08 | g.chr3:47042572G>A | c.4387G>A | c.(4387-4389)Gag>Aag | p.E1463K |
CESC | 3 | 47043554 | 47043554 | + | Missense_Mutation | SNP | G | G | A | TCGA-C5-A2LZ-01A-11D-A20U-09 | TCGA-C5-A2LZ-10B-01D-A20U-09 | g.chr3:47043554G>A | c.4927G>A | c.(4927-4929)Gat>Aat | p.D1643N |
CESC | 3 | 47045644 | 47045644 | + | Missense_Mutation | SNP | G | G | A | TCGA-Q1-A73R-01A-11D-A33O-09 | TCGA-Q1-A73R-10B-01D-A33O-09 | g.chr3:47045644G>A | c.5959G>A | c.(5959-5961)Gca>Aca | p.A1987T |
CESC | 3 | 47047475 | 47047475 | + | Missense_Mutation | SNP | G | G | A | TCGA-FU-A3HZ-01A-11D-A20U-09 | TCGA-FU-A3HZ-10A-01D-A20U-09 | g.chr3:47047475G>A | c.6841G>A | c.(6841-6843)Gac>Aac | p.D2281N |
CESC | 3 | 47049617 | 47049617 | + | Missense_Mutation | SNP | G | G | A | TCGA-C5-A2LZ-01A-11D-A20U-09 | TCGA-C5-A2LZ-10B-01D-A20U-09 | g.chr3:47049617G>A | c.7660G>A | c.(7660-7662)Gct>Act | p.A2554T |
CESC | 3 | 47049909 | 47049909 | + | Missense_Mutation | SNP | C | C | T | TCGA-LP-A4AU-01A-32D-A243-09 | TCGA-LP-A4AU-10A-01D-A243-09 | g.chr3:47049909C>T | c.7856C>T | c.(7855-7857)gCg>gTg | p.A2619V |
COAD | 3 | 47030358 | 47030358 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3994-01A-01W-1073-09 | TCGA-AA-3994-10A-01W-1073-09 | g.chr3:47030358C>T | c.167C>T | c.(166-168)cCg>cTg | p.P56L |
COAD | 3 | 47030775 | 47030775 | + | Missense_Mutation | SNP | G | G | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr3:47030775G>A | c.377G>A | c.(376-378)gGc>gAc | p.G126D |
COAD | 3 | 47032926 | 47032926 | + | Missense_Mutation | SNP | T | T | C | TCGA-D5-6930-01A-11D-1924-10 | TCGA-D5-6930-10A-01D-1924-10 | g.chr3:47032926T>C | c.673T>C | c.(673-675)Tct>Cct | p.S225P |
COAD | 3 | 47033395 | 47033395 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3713-01A-21D-1719-10 | TCGA-AA-3713-11A-01D-1719-10 | g.chr3:47033395A>G | c.991A>G | c.(991-993)Aat>Gat | p.N331D |
COAD | 3 | 47036645 | 47036645 | + | Missense_Mutation | SNP | C | C | T | TCGA-AD-6964-01A-11D-1924-10 | TCGA-AD-6964-10A-01D-1924-10 | g.chr3:47036645C>T | c.1420C>T | c.(1420-1422)Cgc>Tgc | p.R474C |
COAD | 3 | 47037015 | 47037015 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-6781-01A-22D-1924-10 | TCGA-A6-6781-10A-01D-1924-10 | g.chr3:47037015G>A | c.1790G>A | c.(1789-1791)cGa>cAa | p.R597Q |
COAD | 3 | 47037427 | 47037427 | + | Silent | SNP | C | C | T | TCGA-F4-6856-01A-11D-1924-10 | TCGA-F4-6856-10A-01D-1924-10 | g.chr3:47037427C>T | c.2037C>T | c.(2035-2037)tgC>tgT | p.C679C |
COAD | 3 | 47039707 | 47039707 | + | Missense_Mutation | SNP | G | G | A | TCGA-D5-6928-01A-11D-1924-10 | TCGA-D5-6928-10A-01D-1924-10 | g.chr3:47039707G>A | c.3109G>A | c.(3109-3111)Gtg>Atg | p.V1037M |
COAD | 3 | 47040272 | 47040272 | + | Missense_Mutation | SNP | T | T | C | TCGA-AD-6901-01A-11D-1924-10 | TCGA-AD-6901-10A-01D-1924-10 | g.chr3:47040272T>C | c.3287T>C | c.(3286-3288)cTg>cCg | p.L1096P |
COAD | 3 | 47040312 | 47040312 | + | Silent | SNP | C | C | T | TCGA-AA-A022-01A-21W-A096-10 | TCGA-AA-A022-11A-11W-A096-10 | g.chr3:47040312C>T | c.3327C>T | c.(3325-3327)gaC>gaT | p.D1109D |
COAD | 3 | 47040812 | 47040812 | + | Missense_Mutation | SNP | G | G | A | TCGA-CK-5913-01A-11D-1650-10 | TCGA-CK-5913-10A-01D-1650-10 | g.chr3:47040812G>A | c.3551G>A | c.(3550-3552)cGc>cAc | p.R1184H |
COAD | 3 | 47041439 | 47041439 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3715-01A-01W-0900-09 | TCGA-AA-3715-10A-01W-0900-09 | g.chr3:47041439T>C | c.3850T>C | c.(3850-3852)Tgg>Cgg | p.W1284R |
COAD | 3 | 47041622 | 47041622 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-AA-3672-01A-01W-0900-09 | TCGA-AA-3672-10A-01W-0900-09 | g.chr3:47041622delT | c.4033delT | c.(4033-4035)tttfs | p.F1345fs |
COAD | 3 | 47041759 | 47041759 | + | Silent | SNP | G | G | A | TCGA-AA-3715-01A-01W-0900-09 | TCGA-AA-3715-10A-01W-0900-09 | g.chr3:47041759G>A | c.4170G>A | c.(4168-4170)tcG>tcA | p.S1390S |
COAD | 3 | 47042540 | 47042540 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A01R-01A-21W-A096-10 | TCGA-AA-A01R-11A-12W-A096-10 | g.chr3:47042540C>T | c.4355C>T | c.(4354-4356)tCg>tTg | p.S1452L |
COAD | 3 | 47043178 | 47043178 | + | Splice_Site | SNP | G | G | T | TCGA-AA-3815-01A-01W-0995-10 | TCGA-AA-3815-10A-01W-0995-10 | g.chr3:47043178G>T | | c.e30-1 | |
COAD | 3 | 47043264 | 47043264 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3947-01A-01W-0995-10 | TCGA-AA-3947-10A-01W-0995-10 | g.chr3:47043264C>T | c.4730C>T | c.(4729-4731)gCg>gTg | p.A1577V |
COAD | 3 | 47043759 | 47043759 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-6780-01A-11D-1835-10 | TCGA-A6-6780-10A-01D-1835-10 | g.chr3:47043759G>A | c.5132G>A | c.(5131-5133)cGc>cAc | p.R1711H |
COAD | 3 | 47045584 | 47045584 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-6601-01A-11D-1771-10 | TCGA-AZ-6601-11A-01D-1771-10 | g.chr3:47045584C>T | c.5899C>T | c.(5899-5901)Cgg>Tgg | p.R1967W |
COAD | 3 | 47046044 | 47046044 | + | Silent | SNP | G | G | A | TCGA-AA-3949-01A-01W-0995-10 | TCGA-AA-3949-10A-01W-0995-10 | g.chr3:47046044G>A | c.6258G>A | c.(6256-6258)gcG>gcA | p.A2086A |
COAD | 3 | 47048573 | 47048573 | + | Silent | SNP | A | A | G | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr3:47048573A>G | c.7152A>G | c.(7150-7152)gtA>gtG | p.V2384V |
COAD | 3 | 47048602 | 47048602 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3877-01A-01W-0995-10 | TCGA-AA-3877-10A-01W-0995-10 | g.chr3:47048602G>A | c.7181G>A | c.(7180-7182)cGg>cAg | p.R2394Q |
COAD | 3 | 47049804 | 47049804 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3864-01A-01W-0995-10 | TCGA-AA-3864-10A-01W-0995-10 | g.chr3:47049804G>A | c.7751G>A | c.(7750-7752)cGc>cAc | p.R2584H |
COADREAD | 3 | 47030195 | 47030195 | + | Missense_Mutation | SNP | T | T | G | TCGA-AG-A011-01A-01W-A00K-09 | TCGA-AG-A011-10A-01W-A00K-09 | g.chr3:47030195T>G | c.88T>G | c.(88-90)Ttt>Gtt | p.F30V |
COADREAD | 3 | 47030358 | 47030358 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3994-01A-01W-1073-09 | TCGA-AA-3994-10A-01W-1073-09 | g.chr3:47030358C>T | c.167C>T | c.(166-168)cCg>cTg | p.P56L |
COADREAD | 3 | 47030775 | 47030775 | + | Missense_Mutation | SNP | G | G | A | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr3:47030775G>A | c.377G>A | c.(376-378)gGc>gAc | p.G126D |
COADREAD | 3 | 47032926 | 47032926 | + | Missense_Mutation | SNP | T | T | C | TCGA-D5-6930-01A-11D-1924-10 | TCGA-D5-6930-10A-01D-1924-10 | g.chr3:47032926T>C | c.673T>C | c.(673-675)Tct>Cct | p.S225P |
COADREAD | 3 | 47033395 | 47033395 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-3713-01A-21D-1719-10 | TCGA-AA-3713-11A-01D-1719-10 | g.chr3:47033395A>G | c.991A>G | c.(991-993)Aat>Gat | p.N331D |
COADREAD | 3 | 47036645 | 47036645 | + | Missense_Mutation | SNP | C | C | T | TCGA-AD-6964-01A-11D-1924-10 | TCGA-AD-6964-10A-01D-1924-10 | g.chr3:47036645C>T | c.1420C>T | c.(1420-1422)Cgc>Tgc | p.R474C |
COADREAD | 3 | 47037015 | 47037015 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-6781-01A-22D-1924-10 | TCGA-A6-6781-10A-01D-1924-10 | g.chr3:47037015G>A | c.1790G>A | c.(1789-1791)cGa>cAa | p.R597Q |
COADREAD | 3 | 47037427 | 47037427 | + | Silent | SNP | C | C | T | TCGA-F4-6856-01A-11D-1924-10 | TCGA-F4-6856-10A-01D-1924-10 | g.chr3:47037427C>T | c.2037C>T | c.(2035-2037)tgC>tgT | p.C679C |
COADREAD | 3 | 47039707 | 47039707 | + | Missense_Mutation | SNP | G | G | A | TCGA-D5-6928-01A-11D-1924-10 | TCGA-D5-6928-10A-01D-1924-10 | g.chr3:47039707G>A | c.3109G>A | c.(3109-3111)Gtg>Atg | p.V1037M |
COADREAD | 3 | 47039977 | 47039977 | + | Missense_Mutation | SNP | T | T | A | TCGA-AG-A036-01A-12W-A096-10 | TCGA-AG-A036-11A-11W-A096-10 | g.chr3:47039977T>A | c.3143T>A | c.(3142-3144)aTa>aAa | p.I1048K |
COADREAD | 3 | 47040272 | 47040272 | + | Missense_Mutation | SNP | T | T | C | TCGA-AD-6901-01A-11D-1924-10 | TCGA-AD-6901-10A-01D-1924-10 | g.chr3:47040272T>C | c.3287T>C | c.(3286-3288)cTg>cCg | p.L1096P |
COADREAD | 3 | 47040312 | 47040312 | + | Silent | SNP | C | C | T | TCGA-AA-A022-01A-21W-A096-10 | TCGA-AA-A022-11A-11W-A096-10 | g.chr3:47040312C>T | c.3327C>T | c.(3325-3327)gaC>gaT | p.D1109D |
COADREAD | 3 | 47040812 | 47040812 | + | Missense_Mutation | SNP | G | G | A | TCGA-CK-5913-01A-11D-1650-10 | TCGA-CK-5913-10A-01D-1650-10 | g.chr3:47040812G>A | c.3551G>A | c.(3550-3552)cGc>cAc | p.R1184H |
COADREAD | 3 | 47041439 | 47041439 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3715-01A-01W-0900-09 | TCGA-AA-3715-10A-01W-0900-09 | g.chr3:47041439T>C | c.3850T>C | c.(3850-3852)Tgg>Cgg | p.W1284R |
COADREAD | 3 | 47041622 | 47041622 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-AA-3672-01A-01W-0900-09 | TCGA-AA-3672-10A-01W-0900-09 | g.chr3:47041622delT | c.4033delT | c.(4033-4035)tttfs | p.F1345fs |
COADREAD | 3 | 47041759 | 47041759 | + | Silent | SNP | G | G | A | TCGA-AA-3715-01A-01W-0900-09 | TCGA-AA-3715-10A-01W-0900-09 | g.chr3:47041759G>A | c.4170G>A | c.(4168-4170)tcG>tcA | p.S1390S |
COADREAD | 3 | 47042529 | 47042529 | + | Silent | SNP | C | C | T | TCGA-CI-6624-01C-11D-1826-10 | TCGA-CI-6624-10A-01D-1826-10 | g.chr3:47042529C>T | c.4344C>T | c.(4342-4344)aaC>aaT | p.N1448N |
COADREAD | 3 | 47042540 | 47042540 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A01R-01A-21W-A096-10 | TCGA-AA-A01R-11A-12W-A096-10 | g.chr3:47042540C>T | c.4355C>T | c.(4354-4356)tCg>tTg | p.S1452L |
COADREAD | 3 | 47042866 | 47042866 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A02N-01A-11W-A096-10 | TCGA-AG-A02N-11A-11W-A096-10 | g.chr3:47042866C>T | c.4582C>T | c.(4582-4584)Cgt>Tgt | p.R1528C |
COADREAD | 3 | 47043178 | 47043178 | + | Splice_Site | SNP | G | G | T | TCGA-AA-3815-01A-01W-0995-10 | TCGA-AA-3815-10A-01W-0995-10 | g.chr3:47043178G>T | | c.e30-1 | |
COADREAD | 3 | 47043264 | 47043264 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3947-01A-01W-0995-10 | TCGA-AA-3947-10A-01W-0995-10 | g.chr3:47043264C>T | c.4730C>T | c.(4729-4731)gCg>gTg | p.A1577V |
COADREAD | 3 | 47043759 | 47043759 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-6780-01A-11D-1835-10 | TCGA-A6-6780-10A-01D-1835-10 | g.chr3:47043759G>A | c.5132G>A | c.(5131-5133)cGc>cAc | p.R1711H |
COADREAD | 3 | 47045584 | 47045584 | + | Missense_Mutation | SNP | C | C | T | TCGA-AZ-6601-01A-11D-1771-10 | TCGA-AZ-6601-11A-01D-1771-10 | g.chr3:47045584C>T | c.5899C>T | c.(5899-5901)Cgg>Tgg | p.R1967W |
COADREAD | 3 | 47046044 | 47046044 | + | Silent | SNP | G | G | A | TCGA-AA-3949-01A-01W-0995-10 | TCGA-AA-3949-10A-01W-0995-10 | g.chr3:47046044G>A | c.6258G>A | c.(6256-6258)gcG>gcA | p.A2086A |
COADREAD | 3 | 47048573 | 47048573 | + | Silent | SNP | A | A | G | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr3:47048573A>G | c.7152A>G | c.(7150-7152)gtA>gtG | p.V2384V |
COADREAD | 3 | 47048602 | 47048602 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3877-01A-01W-0995-10 | TCGA-AA-3877-10A-01W-0995-10 | g.chr3:47048602G>A | c.7181G>A | c.(7180-7182)cGg>cAg | p.R2394Q |
COADREAD | 3 | 47049804 | 47049804 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3864-01A-01W-0995-10 | TCGA-AA-3864-10A-01W-0995-10 | g.chr3:47049804G>A | c.7751G>A | c.(7750-7752)cGc>cAc | p.R2584H |
DLBC | 3 | 47033970 | 47033970 | + | Silent | SNP | C | C | T | TCGA-G8-6907-01A-11D-2210-10 | TCGA-G8-6907-14A-01D-2210-10 | g.chr3:47033970C>T | c.1038C>T | c.(1036-1038)taC>taT | p.Y346Y |
DLBC | 3 | 47046485 | 47046485 | + | Silent | SNP | C | C | T | TCGA-GR-7351-01A-11D-2210-10 | TCGA-GR-7351-10A-01D-2210-10 | g.chr3:47046485C>T | c.6318C>T | c.(6316-6318)taC>taT | p.Y2106Y |
ESCA | 3 | 47033032 | 47033032 | + | Missense_Mutation | SNP | T | T | C | TCGA-L5-A8NM-01A-11D-A37C-09 | TCGA-L5-A8NM-11A-12D-A37F-09 | g.chr3:47033032T>C | c.779T>C | c.(778-780)gTc>gCc | p.V260A |
ESCA | 3 | 47036669 | 47036669 | + | Missense_Mutation | SNP | T | T | C | TCGA-2H-A9GM-01A-11D-A37C-09 | TCGA-2H-A9GM-11A-11D-A37F-09 | g.chr3:47036669T>C | c.1444T>C | c.(1444-1446)Tgc>Cgc | p.C482R |
ESCA | 3 | 47037271 | 47037271 | + | Missense_Mutation | SNP | G | G | T | TCGA-L5-A43C-01A-11D-A247-09 | TCGA-L5-A43C-11A-11D-A247-09 | g.chr3:47037271G>T | c.1966G>T | c.(1966-1968)Gtg>Ttg | p.V656L |
ESCA | 3 | 47039969 | 47039969 | + | Missense_Mutation | SNP | G | G | T | TCGA-LN-A49L-01A-11D-A247-09 | TCGA-LN-A49L-10A-01D-A247-09 | g.chr3:47039969G>T | c.3135G>T | c.(3133-3135)atG>atT | p.M1045I |
ESCA | 3 | 47040003 | 47040003 | + | Missense_Mutation | SNP | C | C | T | TCGA-L5-A8NM-01A-11D-A37C-09 | TCGA-L5-A8NM-11A-12D-A37F-09 | g.chr3:47040003C>T | c.3169C>T | c.(3169-3171)Cgg>Tgg | p.R1057W |
ESCA | 3 | 47040460 | 47040460 | + | Silent | SNP | G | G | A | TCGA-L5-A4OW-01A-11D-A28B-09 | TCGA-L5-A4OW-11A-11D-A28E-09 | g.chr3:47040460G>A | c.3396G>A | c.(3394-3396)gcG>gcA | p.A1132A |
ESCA | 3 | 47041439 | 47041439 | + | Missense_Mutation | SNP | T | T | A | TCGA-L5-A4OI-01A-11D-A27G-09 | TCGA-L5-A4OI-11A-11D-A27G-09 | g.chr3:47041439T>A | c.3850T>A | c.(3850-3852)Tgg>Agg | p.W1284R |
ESCA | 3 | 47044496 | 47044496 | + | Missense_Mutation | SNP | C | C | T | TCGA-LN-A7HY-01A-12D-A351-09 | TCGA-LN-A7HY-10A-01D-A351-09 | g.chr3:47044496C>T | c.5509C>T | c.(5509-5511)Cgc>Tgc | p.R1837C |
ESCA | 3 | 47044771 | 47044771 | + | Missense_Mutation | SNP | G | G | A | TCGA-L5-A4ON-01A-11D-A27G-09 | TCGA-L5-A4ON-11A-21D-A27G-09 | g.chr3:47044771G>A | c.5692G>A | c.(5692-5694)Gag>Aag | p.E1898K |
ESCA | 3 | 47045639 | 47045639 | + | Missense_Mutation | SNP | G | G | T | TCGA-V5-AASV-01A-11D-A387-09 | TCGA-V5-AASV-10A-01D-A38A-09 | g.chr3:47045639G>T | c.5954G>T | c.(5953-5955)cGt>cTt | p.R1985L |
ESCA | 3 | 47049918 | 47049918 | + | Missense_Mutation | SNP | G | G | A | TCGA-LN-A9FQ-01A-31D-A387-09 | TCGA-LN-A9FQ-10A-01D-A38A-09 | g.chr3:47049918G>A | c.7865G>A | c.(7864-7866)cGt>cAt | p.R2622H |
GBM | 3 | 47040042 | 47040042 | + | Missense_Mutation | SNP | C | C | T | TCGA-06-5858-01A-01D-1696-08 | TCGA-06-5858-10A-01D-1696-08 | g.chr3:47040042C>T | c.3208C>T | c.(3208-3210)Cgc>Tgc | p.R1070C |
GBM | 3 | 47040321 | 47040321 | + | Silent | SNP | C | C | T | TCGA-26-6173-01A-11D-1845-08 | TCGA-26-6173-10A-01D-1845-08 | g.chr3:47040321C>T | c.3336C>T | c.(3334-3336)gtC>gtT | p.V1112V |
GBM | 3 | 47041457 | 47041457 | + | Missense_Mutation | SNP | C | C | T | TCGA-32-4211-01A-01D-1353-08 | TCGA-32-4211-10A-01D-1353-08 | g.chr3:47041457C>T | c.3868C>T | c.(3868-3870)Cgg>Tgg | p.R1290W |
GBM | 3 | 47041686 | 47041686 | + | Missense_Mutation | SNP | G | G | T | TCGA-06-6697-01A-11D-1845-08 | TCGA-06-6697-10A-01D-1845-08 | g.chr3:47041686G>T | c.4097G>T | c.(4096-4098)gGa>gTa | p.G1366V |
GBMLGG | 3 | 47037063 | 47037063 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr3:47037063C>T | c.1838C>T | c.(1837-1839)cCt>cTt | p.P613L |
GBMLGG | 3 | 47038035 | 47038035 | + | Missense_Mutation | SNP | T | T | C | TCGA-HT-7477-01B-11D-A289-08 | TCGA-HT-7477-10A-01D-A289-08 | g.chr3:47038035T>C | c.2426T>C | c.(2425-2427)tTt>tCt | p.F809S |
GBMLGG | 3 | 47040042 | 47040042 | + | Missense_Mutation | SNP | C | C | T | TCGA-06-5858-01A-01D-1696-08 | TCGA-06-5858-10A-01D-1696-08 | g.chr3:47040042C>T | c.3208C>T | c.(3208-3210)Cgc>Tgc | p.R1070C |
GBMLGG | 3 | 47040321 | 47040321 | + | Silent | SNP | C | C | T | TCGA-26-6173-01A-11D-1845-08 | TCGA-26-6173-10A-01D-1845-08 | g.chr3:47040321C>T | c.3336C>T | c.(3334-3336)gtC>gtT | p.V1112V |
GBMLGG | 3 | 47040555 | 47040555 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-E1-A7YJ-01A-11D-A34A-08 | TCGA-E1-A7YJ-10A-01D-A34A-08 | g.chr3:47040555delC | c.3491delC | c.(3490-3492)gccfs | p.A1164fs |
GBMLGG | 3 | 47041457 | 47041457 | + | Missense_Mutation | SNP | C | C | T | TCGA-32-4211-01A-01D-1353-08 | TCGA-32-4211-10A-01D-1353-08 | g.chr3:47041457C>T | c.3868C>T | c.(3868-3870)Cgg>Tgg | p.R1290W |
GBMLGG | 3 | 47041457 | 47041457 | + | Missense_Mutation | SNP | C | C | T | TCGA-DH-5144-01A-01D-1468-08 | TCGA-DH-5144-10A-01D-1468-08 | g.chr3:47041457C>T | c.3868C>T | c.(3868-3870)Cgg>Tgg | p.R1290W |
GBMLGG | 3 | 47041686 | 47041686 | + | Missense_Mutation | SNP | G | G | T | TCGA-06-6697-01A-11D-1845-08 | TCGA-06-6697-10A-01D-1845-08 | g.chr3:47041686G>T | c.4097G>T | c.(4096-4098)gGa>gTa | p.G1366V |
GBMLGG | 3 | 47041884 | 47041884 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr3:47041884G>A | c.4295G>A | c.(4294-4296)aGc>aAc | p.S1432N |
GBMLGG | 3 | 47043273 | 47043273 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr3:47043273G>A | c.4739G>A | c.(4738-4740)gGc>gAc | p.G1580D |
GBMLGG | 3 | 47044503 | 47044503 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr3:47044503G>A | c.5516G>A | c.(5515-5517)cGt>cAt | p.R1839H |
GBMLGG | 3 | 47050155 | 47050155 | + | Missense_Mutation | SNP | A | A | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr3:47050155A>G | c.8024A>G | c.(8023-8025)aAc>aGc | p.N2675S |
HNSC | 3 | 47030591 | 47030591 | + | Missense_Mutation | SNP | G | G | C | TCGA-CN-6011-01A-11D-1683-08 | TCGA-CN-6011-10A-01D-1683-08 | g.chr3:47030591G>C | c.286G>C | c.(286-288)Gag>Cag | p.E96Q |
HNSC | 3 | 47033992 | 47033992 | + | Missense_Mutation | SNP | G | G | A | TCGA-CV-6936-01A-11D-1912-08 | TCGA-CV-6936-10A-01D-1912-08 | g.chr3:47033992G>A | c.1060G>A | c.(1060-1062)Gag>Aag | p.E354K |
HNSC | 3 | 47037517 | 47037517 | + | Silent | SNP | C | C | T | TCGA-D6-6516-01A-11D-1870-08 | TCGA-D6-6516-10A-01D-1870-08 | g.chr3:47037517C>T | c.2127C>T | c.(2125-2127)ccC>ccT | p.P709P |
HNSC | 3 | 47037919 | 47037919 | + | Silent | SNP | C | C | T | TCGA-CN-4730-01A-01D-1434-08 | TCGA-CN-4730-10A-01D-1434-08 | g.chr3:47037919C>T | c.2310C>T | c.(2308-2310)tcC>tcT | p.S770S |
HNSC | 3 | 47040353 | 47040353 | + | Missense_Mutation | SNP | C | C | T | TCGA-QK-A6VB-01A-12D-A34J-08 | TCGA-QK-A6VB-10B-01D-A34M-08 | g.chr3:47040353C>T | c.3368C>T | c.(3367-3369)aCa>aTa | p.T1123I |
HNSC | 3 | 47041650 | 47041650 | + | Missense_Mutation | SNP | C | C | T | TCGA-CV-7425-01A-11D-2078-08 | TCGA-CV-7425-10A-01D-2078-08 | g.chr3:47041650C>T | c.4061C>T | c.(4060-4062)aCg>aTg | p.T1354M |
HNSC | 3 | 47041666 | 47041666 | + | Silent | SNP | C | C | A | TCGA-BA-A6DL-01A-21D-A30E-08 | TCGA-BA-A6DL-10A-01D-A30H-08 | g.chr3:47041666C>A | c.4077C>A | c.(4075-4077)ggC>ggA | p.G1359G |
HNSC | 3 | 47043455 | 47043455 | + | Missense_Mutation | SNP | G | G | A | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr3:47043455G>A | c.4828G>A | c.(4828-4830)Gca>Aca | p.A1610T |
HNSC | 3 | 47044464 | 47044464 | + | Missense_Mutation | SNP | G | G | A | TCGA-CQ-5323-01A-01D-1683-08 | TCGA-CQ-5323-10A-01D-1683-08 | g.chr3:47044464G>A | c.5477G>A | c.(5476-5478)cGc>cAc | p.R1826H |
HNSC | 3 | 47045664 | 47045664 | + | Silent | SNP | C | C | T | TCGA-CN-4723-01A-01D-1434-08 | TCGA-CN-4723-10A-01D-1434-08 | g.chr3:47045664C>T | c.5979C>T | c.(5977-5979)atC>atT | p.I1993I |
HNSC | 3 | 47049354 | 47049354 | + | Nonsense_Mutation | SNP | C | C | G | TCGA-CR-7374-01A-11D-2012-08 | TCGA-CR-7374-10A-01D-2013-08 | g.chr3:47049354C>G | c.7556C>G | c.(7555-7557)tCa>tGa | p.S2519* |
HNSC | 3 | 47049787 | 47049787 | + | Missense_Mutation | SNP | C | C | G | TCGA-CR-7374-01A-11D-2012-08 | TCGA-CR-7374-10A-01D-2013-08 | g.chr3:47049787C>G | c.7734C>G | c.(7732-7734)atC>atG | p.I2578M |
KICH | 3 | 47041771 | 47041771 | + | Silent | SNP | G | G | A | TCGA-KM-8443-01A-11D-2310-10 | TCGA-KM-8443-10A-01D-2311-10 | g.chr3:47041771G>A | c.4182G>A | c.(4180-4182)ggG>ggA | p.G1394G |
KICH | 3 | 47042507 | 47042507 | + | Missense_Mutation | SNP | A | A | G | TCGA-KN-8433-01A-11D-2310-10 | TCGA-KN-8433-11A-01D-2311-10 | g.chr3:47042507A>G | c.4322A>G | c.(4321-4323)gAg>gGg | p.E1441G |
KIPAN | 3 | 47032943 | 47032943 | + | Silent | SNP | G | G | T | TCGA-BQ-5890-01A-11D-1589-08 | TCGA-BQ-5890-11A-01D-1589-08 | g.chr3:47032943G>T | c.690G>T | c.(688-690)ctG>ctT | p.L230L |
KIPAN | 3 | 47037324 | 47037324 | + | Silent | SNP | C | C | G | TCGA-CZ-5458-01A-01D-1501-10 | TCGA-CZ-5458-11A-01D-1501-10 | g.chr3:47037324C>G | c.2019C>G | c.(2017-2019)gcC>gcG | p.A673A |
KIPAN | 3 | 47038048 | 47038048 | + | Silent | SNP | G | G | A | TCGA-BP-4976-01A-01D-1462-08 | TCGA-BP-4976-11A-01D-1462-08 | g.chr3:47038048G>A | c.2439G>A | c.(2437-2439)ctG>ctA | p.L813L |
KIPAN | 3 | 47038846 | 47038846 | + | Missense_Mutation | SNP | C | C | T | TCGA-Y8-A8RY-01A-11D-A36X-10 | TCGA-Y8-A8RY-10A-01D-A370-10 | g.chr3:47038846C>T | c.2747C>T | c.(2746-2748)aCg>aTg | p.T916M |
KIPAN | 3 | 47041771 | 47041771 | + | Silent | SNP | G | G | A | TCGA-KM-8443-01A-11D-2310-10 | TCGA-KM-8443-10A-01D-2311-10 | g.chr3:47041771G>A | c.4182G>A | c.(4180-4182)ggG>ggA | p.G1394G |
KIPAN | 3 | 47042507 | 47042507 | + | Missense_Mutation | SNP | A | A | G | TCGA-KN-8433-01A-11D-2310-10 | TCGA-KN-8433-11A-01D-2311-10 | g.chr3:47042507A>G | c.4322A>G | c.(4321-4323)gAg>gGg | p.E1441G |
KIPAN | 3 | 47043759 | 47043759 | + | Missense_Mutation | SNP | G | G | A | TCGA-BP-4998-01A-01D-1462-08 | TCGA-BP-4998-11A-01D-1462-08 | g.chr3:47043759G>A | c.5132G>A | c.(5131-5133)cGc>cAc | p.R1711H |
KIPAN | 3 | 47049869 | 47049869 | + | Missense_Mutation | SNP | G | G | A | TCGA-DZ-6133-01A-11D-1961-08 | TCGA-DZ-6133-10A-01D-1962-08 | g.chr3:47049869G>A | c.7816G>A | c.(7816-7818)Gca>Aca | p.A2606T |
KIPAN | 3 | 47050126 | 47050126 | + | Silent | SNP | C | C | A | TCGA-BP-4158-01A-02D-1366-10 | TCGA-BP-4158-11A-01D-1366-10 | g.chr3:47050126C>A | c.7995C>A | c.(7993-7995)gcC>gcA | p.A2665A |
KIRC | 3 | 47037324 | 47037324 | + | Silent | SNP | C | C | G | TCGA-CZ-5458-01A-01D-1501-10 | TCGA-CZ-5458-11A-01D-1501-10 | g.chr3:47037324C>G | c.2019C>G | c.(2017-2019)gcC>gcG | p.A673A |
KIRC | 3 | 47038048 | 47038048 | + | Silent | SNP | G | G | A | TCGA-BP-4976-01A-01D-1462-08 | TCGA-BP-4976-11A-01D-1462-08 | g.chr3:47038048G>A | c.2439G>A | c.(2437-2439)ctG>ctA | p.L813L |
KIRC | 3 | 47043759 | 47043759 | + | Missense_Mutation | SNP | G | G | A | TCGA-BP-4998-01A-01D-1462-08 | TCGA-BP-4998-11A-01D-1462-08 | g.chr3:47043759G>A | c.5132G>A | c.(5131-5133)cGc>cAc | p.R1711H |
KIRC | 3 | 47050126 | 47050126 | + | Silent | SNP | C | C | A | TCGA-BP-4158-01A-02D-1366-10 | TCGA-BP-4158-11A-01D-1366-10 | g.chr3:47050126C>A | c.7995C>A | c.(7993-7995)gcC>gcA | p.A2665A |
KIRP | 3 | 47032943 | 47032943 | + | Silent | SNP | G | G | T | TCGA-BQ-5890-01A-11D-1589-08 | TCGA-BQ-5890-11A-01D-1589-08 | g.chr3:47032943G>T | c.690G>T | c.(688-690)ctG>ctT | p.L230L |
KIRP | 3 | 47038846 | 47038846 | + | Missense_Mutation | SNP | C | C | T | TCGA-Y8-A8RY-01A-11D-A36X-10 | TCGA-Y8-A8RY-10A-01D-A370-10 | g.chr3:47038846C>T | c.2747C>T | c.(2746-2748)aCg>aTg | p.T916M |
KIRP | 3 | 47049869 | 47049869 | + | Missense_Mutation | SNP | G | G | A | TCGA-DZ-6133-01A-11D-1961-08 | TCGA-DZ-6133-10A-01D-1962-08 | g.chr3:47049869G>A | c.7816G>A | c.(7816-7818)Gca>Aca | p.A2606T |
LGG | 3 | 47037063 | 47037063 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr3:47037063C>T | c.1838C>T | c.(1837-1839)cCt>cTt | p.P613L |
LGG | 3 | 47038035 | 47038035 | + | Missense_Mutation | SNP | T | T | C | TCGA-HT-7477-01B-11D-A289-08 | TCGA-HT-7477-10A-01D-A289-08 | g.chr3:47038035T>C | c.2426T>C | c.(2425-2427)tTt>tCt | p.F809S |
LGG | 3 | 47040555 | 47040555 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-E1-A7YJ-01A-11D-A34A-08 | TCGA-E1-A7YJ-10A-01D-A34A-08 | g.chr3:47040555delC | c.3491delC | c.(3490-3492)gccfs | p.A1164fs |
LGG | 3 | 47041457 | 47041457 | + | Missense_Mutation | SNP | C | C | T | TCGA-DH-5144-01A-01D-1468-08 | TCGA-DH-5144-10A-01D-1468-08 | g.chr3:47041457C>T | c.3868C>T | c.(3868-3870)Cgg>Tgg | p.R1290W |
LGG | 3 | 47041884 | 47041884 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr3:47041884G>A | c.4295G>A | c.(4294-4296)aGc>aAc | p.S1432N |
LGG | 3 | 47043273 | 47043273 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr3:47043273G>A | c.4739G>A | c.(4738-4740)gGc>gAc | p.G1580D |
LGG | 3 | 47044503 | 47044503 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr3:47044503G>A | c.5516G>A | c.(5515-5517)cGt>cAt | p.R1839H |
LGG | 3 | 47050155 | 47050155 | + | Missense_Mutation | SNP | A | A | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr3:47050155A>G | c.8024A>G | c.(8023-8025)aAc>aGc | p.N2675S |
LIHC | 3 | 47030821 | 47030821 | + | Silent | SNP | C | C | G | TCGA-BC-A217-01A-11D-A152-10 | TCGA-BC-A217-10A-01D-A152-10 | g.chr3:47030821C>G | c.423C>G | c.(421-423)ctC>ctG | p.L141L |
LIHC | 3 | 47037989 | 47037989 | + | Missense_Mutation | SNP | G | G | T | TCGA-DD-A3A8-01A-11D-A22F-10 | TCGA-DD-A3A8-11A-11D-A22F-10 | g.chr3:47037989G>T | c.2380G>T | c.(2380-2382)Ggc>Tgc | p.G794C |
LIHC | 3 | 47040568 | 47040568 | + | Silent | SNP | G | G | T | TCGA-ES-A2HT-01A-12D-A183-10 | TCGA-ES-A2HT-11A-11D-A183-10 | g.chr3:47040568G>T | c.3504G>T | c.(3502-3504)cgG>cgT | p.R1168R |
LIHC | 3 | 47042832 | 47042832 | + | Silent | SNP | G | G | T | TCGA-CC-A7IH-01A-11D-A33K-10 | TCGA-CC-A7IH-10A-01D-A33K-10 | g.chr3:47042832G>T | c.4548G>T | c.(4546-4548)ctG>ctT | p.L1516L |
LIHC | 3 | 47043918 | 47043918 | + | Missense_Mutation | SNP | A | A | T | TCGA-DD-A119-01A-11D-A12Z-10 | TCGA-DD-A119-10A-01D-A12Z-10 | g.chr3:47043918A>T | c.5209A>T | c.(5209-5211)Atg>Ttg | p.M1737L |
LIHC | 3 | 47043973 | 47043973 | + | Missense_Mutation | SNP | G | G | T | TCGA-CC-A7IG-01A-11D-A33K-10 | TCGA-CC-A7IG-10A-01D-A33K-10 | g.chr3:47043973G>T | c.5264G>T | c.(5263-5265)cGc>cTc | p.R1755L |
LIHC | 3 | 47044767 | 47044767 | + | Silent | SNP | C | C | T | TCGA-DD-AADS-01A-11D-A40R-10 | TCGA-DD-AADS-10A-01D-A40U-10 | g.chr3:47044767C>T | c.5688C>T | c.(5686-5688)ctC>ctT | p.L1896L |
LIHC | 3 | 47046023 | 47046023 | + | Missense_Mutation | SNP | G | G | T | TCGA-EP-A2KA-01A-11D-A183-10 | TCGA-EP-A2KA-10A-01D-A183-10 | g.chr3:47046023G>T | c.6237G>T | c.(6235-6237)ttG>ttT | p.L2079F |
LIHC | 3 | 47046579 | 47046579 | + | Silent | SNP | A | A | C | TCGA-2Y-A9GT-01A-11D-A382-10 | TCGA-2Y-A9GT-10A-01D-A385-10 | g.chr3:47046579A>C | c.6412A>C | c.(6412-6414)Agg>Cgg | p.R2138R |
LIHC | 3 | 47047032 | 47047032 | + | Missense_Mutation | SNP | G | G | T | TCGA-4R-AA8I-01A-11D-A382-10 | TCGA-4R-AA8I-10B-01D-A385-10 | g.chr3:47047032G>T | c.6614G>T | c.(6613-6615)cGc>cTc | p.R2205L |
LIHC | 3 | 47049823 | 47049823 | + | Silent | SNP | A | A | G | TCGA-WX-AA44-01A-11D-A38X-10 | TCGA-WX-AA44-10A-01D-A38X-10 | g.chr3:47049823A>G | c.7770A>G | c.(7768-7770)gcA>gcG | p.A2590A |
LUAD | 3 | 47030766 | 47030766 | + | Missense_Mutation | SNP | C | C | G | TCGA-55-A490-01A-11D-A24D-08 | TCGA-55-A490-10A-01D-A24F-08 | g.chr3:47030766C>G | c.368C>G | c.(367-369)cCa>cGa | p.P123R |
LUAD | 3 | 47032756 | 47032756 | + | Missense_Mutation | SNP | C | C | T | TCGA-67-4679-01B-01D-1753-08 | TCGA-67-4679-10A-01D-1753-08 | g.chr3:47032756C>T | c.604C>T | c.(604-606)Ctc>Ttc | p.L202F |
LUAD | 3 | 47037012 | 47037012 | + | Missense_Mutation | SNP | A | A | C | TCGA-55-8089-01A-11D-2238-08 | TCGA-55-8089-10A-01D-2238-08 | g.chr3:47037012A>C | c.1787A>C | c.(1786-1788)cAg>cCg | p.Q596P |
LUAD | 3 | 47037035 | 47037035 | + | Missense_Mutation | SNP | A | A | T | TCGA-86-A456-01A-11D-A24D-08 | TCGA-86-A456-10A-01D-A24F-08 | g.chr3:47037035A>T | c.1810A>T | c.(1810-1812)Acc>Tcc | p.T604S |
LUAD | 3 | 47037928 | 47037928 | + | Silent | SNP | G | G | T | TCGA-55-8094-01A-11D-2238-08 | TCGA-55-8094-10A-01D-2238-08 | g.chr3:47037928G>T | c.2319G>T | c.(2317-2319)gtG>gtT | p.V773V |
LUAD | 3 | 47039673 | 47039673 | + | Silent | SNP | C | C | T | TCGA-55-6972-01A-11D-1945-08 | TCGA-55-6972-11A-01D-1945-08 | g.chr3:47039673C>T | c.3075C>T | c.(3073-3075)ttC>ttT | p.F1025F |
LUAD | 3 | 47041640 | 47041640 | + | Missense_Mutation | SNP | C | C | G | TCGA-91-8497-01A-11D-2393-08 | TCGA-91-8497-10A-01D-2393-08 | g.chr3:47041640C>G | c.4051C>G | c.(4051-4053)Cca>Gca | p.P1351A |
LUAD | 3 | 47042584 | 47042584 | + | Missense_Mutation | SNP | C | C | T | TCGA-55-8620-01A-11D-2393-08 | TCGA-55-8620-10A-01D-2393-08 | g.chr3:47042584C>T | c.4399C>T | c.(4399-4401)Cgg>Tgg | p.R1467W |
LUAD | 3 | 47042821 | 47042821 | + | Missense_Mutation | SNP | G | G | A | TCGA-55-7576-01A-11D-2063-08 | TCGA-55-7576-10A-01D-2063-08 | g.chr3:47042821G>A | c.4537G>A | c.(4537-4539)Gtg>Atg | p.V1513M |
LUAD | 3 | 47043987 | 47043987 | + | Missense_Mutation | SNP | G | G | T | TCGA-05-4415-01A-22D-1855-08 | TCGA-05-4415-10A-01D-1855-08 | g.chr3:47043987G>T | c.5278G>T | c.(5278-5280)Gcc>Tcc | p.A1760S |
LUAD | 3 | 47044463 | 47044463 | + | Missense_Mutation | SNP | C | C | T | TCGA-75-5126-01A-01D-1753-08 | TCGA-75-5126-10A-01D-1753-08 | g.chr3:47044463C>T | c.5476C>T | c.(5476-5478)Cgc>Tgc | p.R1826C |
LUAD | 3 | 47044544 | 47044544 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-95-7562-01A-11D-2238-08 | TCGA-95-7562-10B-01D-2238-08 | g.chr3:47044544G>T | c.5557G>T | c.(5557-5559)Gaa>Taa | p.E1853* |
LUAD | 3 | 47044777 | 47044777 | + | Missense_Mutation | SNP | G | G | A | TCGA-05-5428-01A-01D-1625-08 | TCGA-05-5428-10A-01D-1625-08 | g.chr3:47044777G>A | c.5698G>A | c.(5698-5700)Gag>Aag | p.E1900K |
LUAD | 3 | 47047932 | 47047932 | + | Missense_Mutation | SNP | T | T | A | TCGA-91-A4BC-01A-11D-A24D-08 | TCGA-91-A4BC-10A-01D-A24F-08 | g.chr3:47047932T>A | c.7127T>A | c.(7126-7128)tTc>tAc | p.F2376Y |
LUSC | 3 | 47030752 | 47030752 | + | Silent | SNP | G | G | T | TCGA-18-3421-01A-01D-0983-08 | TCGA-18-3421-11A-01D-0983-08 | g.chr3:47030752G>T | c.354G>T | c.(352-354)ctG>ctT | p.L118L |
LUSC | 3 | 47037075 | 47037075 | + | Missense_Mutation | SNP | C | C | T | TCGA-22-1016-01A-01D-1521-08 | TCGA-22-1016-11A-01D-1521-08 | g.chr3:47037075C>T | c.1850C>T | c.(1849-1851)gCa>gTa | p.A617V |
LUSC | 3 | 47043973 | 47043973 | + | Missense_Mutation | SNP | G | G | A | TCGA-21-1076-01A-02D-1521-08 | TCGA-21-1076-11A-01D-1521-08 | g.chr3:47043973G>A | c.5264G>A | c.(5263-5265)cGc>cAc | p.R1755H |
LUSC | 3 | 47044477 | 47044477 | + | Silent | SNP | C | C | A | TCGA-18-3409-01A-01D-0983-08 | TCGA-18-3409-11A-01D-0983-08 | g.chr3:47044477C>A | c.5490C>A | c.(5488-5490)tcC>tcA | p.S1830S |
LUSC | 3 | 47045732 | 47045732 | + | Missense_Mutation | SNP | A | A | G | TCGA-22-4591-01A-01D-1267-08 | TCGA-22-4591-11A-01D-1267-08 | g.chr3:47045732A>G | c.6047A>G | c.(6046-6048)cAg>cGg | p.Q2016R |
OV | 3 | 47050489 | 47050489 | + | Missense_Mutation | SNP | G | G | A | TCGA-24-1470-01A-01W-0553-09 | TCGA-24-1470-10A-01W-0553-09 | g.chr3:47050489G>A | c.8038G>A | c.(8038-8040)Gcc>Acc | p.A2680T |
PAAD | 3 | 47030423 | 47030423 | + | Missense_Mutation | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr3:47030423G>A | c.232G>A | c.(232-234)Gcc>Acc | p.A78T |
PAAD | 3 | 47040450 | 47040450 | + | Splice_Site | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr3:47040450C>T | c.3386C>T | c.(3385-3387)gCg>gTg | p.A1129V |
PAAD | 3 | 47041634 | 47041634 | + | Missense_Mutation | SNP | C | C | G | TCGA-2J-AABK-01A-31D-A40W-08 | TCGA-2J-AABK-10A-01D-A40W-08 | g.chr3:47041634C>G | c.4045C>G | c.(4045-4047)Ctc>Gtc | p.L1349V |
PAAD | 3 | 47041693 | 47041693 | + | Silent | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr3:47041693C>T | c.4104C>T | c.(4102-4104)ggC>ggT | p.G1368G |
PAAD | 3 | 47042768 | 47042768 | + | Splice_Site | SNP | G | G | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr3:47042768G>T | | c.e29-1 | |
PAAD | 3 | 47047546 | 47047546 | + | Silent | SNP | C | C | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr3:47047546C>A | c.6912C>A | c.(6910-6912)acC>acA | p.T2304T |
PAAD | 3 | 47049628 | 47049628 | + | Silent | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr3:47049628C>T | c.7671C>T | c.(7669-7671)agC>agT | p.S2557S |
PCPG | 3 | 47041446 | 47041446 | + | Missense_Mutation | SNP | A | A | T | TCGA-QR-A70R-01A-11D-A35D-08 | TCGA-QR-A70R-10A-01D-A35B-08 | g.chr3:47041446A>T | c.3857A>T | c.(3856-3858)gAt>gTt | p.D1286V |
PCPG | 3 | 47043265 | 47043265 | + | Silent | SNP | G | G | A | TCGA-QT-A5XL-01A-11D-A35D-08 | TCGA-QT-A5XL-10A-01D-A35B-08 | g.chr3:47043265G>A | c.4731G>A | c.(4729-4731)gcG>gcA | p.A1577A |
PRAD | 3 | 47036899 | 47036899 | + | Silent | SNP | A | A | G | TCGA-EJ-5507-01A-01D-1576-08 | TCGA-EJ-5507-10A-01D-1577-08 | g.chr3:47036899A>G | c.1674A>G | c.(1672-1674)gcA>gcG | p.A558A |
PRAD | 3 | 47037252 | 47037252 | + | Silent | SNP | C | C | T | TCGA-XJ-A83H-01A-11D-A34U-08 | TCGA-XJ-A83H-10A-01D-A34X-08 | g.chr3:47037252C>T | c.1947C>T | c.(1945-1947)gcC>gcT | p.A649A |
PRAD | 3 | 47038461 | 47038461 | + | Silent | SNP | C | C | A | TCGA-KK-A6E1-01A-11D-A30X-08 | TCGA-KK-A6E1-11A-21D-A30X-08 | g.chr3:47038461C>A | c.2574C>A | c.(2572-2574)atC>atA | p.I858I |
PRAD | 3 | 47041142 | 47041142 | + | Silent | SNP | G | G | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr3:47041142G>A | c.3726G>A | c.(3724-3726)ctG>ctA | p.L1242L |
PRAD | 3 | 47042568 | 47042568 | + | Silent | SNP | C | C | T | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr3:47042568C>T | c.4383C>T | c.(4381-4383)agC>agT | p.S1461S |
PRAD | 3 | 47043455 | 47043455 | + | Missense_Mutation | SNP | G | G | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr3:47043455G>A | c.4828G>A | c.(4828-4830)Gca>Aca | p.A1610T |
PRAD | 3 | 47043892 | 47043892 | + | Missense_Mutation | SNP | A | A | G | TCGA-EJ-5494-01A-01D-1576-08 | TCGA-EJ-5494-10A-01D-1577-08 | g.chr3:47043892A>G | c.5183A>G | c.(5182-5184)gAc>gGc | p.D1728G |
PRAD | 3 | 47047523 | 47047523 | + | Missense_Mutation | SNP | C | C | T | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr3:47047523C>T | c.6889C>T | c.(6889-6891)Ctc>Ttc | p.L2297F |
PRAD | 3 | 47049635 | 47049635 | + | Missense_Mutation | SNP | G | G | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr3:47049635G>A | c.7678G>A | c.(7678-7680)Gcc>Acc | p.A2560T |
PRAD | 3 | 47049880 | 47049880 | + | Silent | SNP | C | C | T | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr3:47049880C>T | c.7827C>T | c.(7825-7827)tcC>tcT | p.S2609S |
READ | 3 | 47030195 | 47030195 | + | Missense_Mutation | SNP | T | T | G | TCGA-AG-A011-01A-01W-A00K-09 | TCGA-AG-A011-10A-01W-A00K-09 | g.chr3:47030195T>G | c.88T>G | c.(88-90)Ttt>Gtt | p.F30V |
READ | 3 | 47039977 | 47039977 | + | Missense_Mutation | SNP | T | T | A | TCGA-AG-A036-01A-12W-A096-10 | TCGA-AG-A036-11A-11W-A096-10 | g.chr3:47039977T>A | c.3143T>A | c.(3142-3144)aTa>aAa | p.I1048K |
READ | 3 | 47042529 | 47042529 | + | Silent | SNP | C | C | T | TCGA-CI-6624-01C-11D-1826-10 | TCGA-CI-6624-10A-01D-1826-10 | g.chr3:47042529C>T | c.4344C>T | c.(4342-4344)aaC>aaT | p.N1448N |
READ | 3 | 47042866 | 47042866 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A02N-01A-11W-A096-10 | TCGA-AG-A02N-11A-11W-A096-10 | g.chr3:47042866C>T | c.4582C>T | c.(4582-4584)Cgt>Tgt | p.R1528C |
SARC | 3 | 47045620 | 47045620 | + | Missense_Mutation | SNP | C | C | T | TCGA-WP-A9GB-01A-11D-A37C-09 | TCGA-WP-A9GB-10A-01D-A37F-09 | g.chr3:47045620C>T | c.5935C>T | c.(5935-5937)Cgg>Tgg | p.R1979W |
SARC | 3 | 47047004 | 47047004 | + | Missense_Mutation | SNP | C | C | T | TCGA-QC-A7B5-01A-11D-A33E-09 | TCGA-QC-A7B5-11A-11D-A33H-09 | g.chr3:47047004C>T | c.6586C>T | c.(6586-6588)Cac>Tac | p.H2196Y |
SKCM | 3 | 47030212 | 47030212 | + | Silent | SNP | G | G | A | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr3:47030212G>A | c.105G>A | c.(103-105)aaG>aaA | p.K35K |
SKCM | 3 | 47030424 | 47030424 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29D-06A-11D-A197-08 | TCGA-EE-A29D-10A-01D-A199-08 | g.chr3:47030424C>T | c.233C>T | c.(232-234)gCc>gTc | p.A78V |
SKCM | 3 | 47031040 | 47031040 | + | Silent | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr3:47031040C>T | c.513C>T | c.(511-513)ttC>ttT | p.F171F |
SKCM | 3 | 47033073 | 47033073 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A181-06A-11D-A196-08 | TCGA-EE-A181-10A-01D-A198-08 | g.chr3:47033073C>T | c.820C>T | c.(820-822)Cgt>Tgt | p.R274C |
SKCM | 3 | 47033334 | 47033334 | + | Silent | SNP | C | C | T | TCGA-ER-A2NC-06A-11D-A197-08 | TCGA-ER-A2NC-10A-01D-A199-08 | g.chr3:47033334C>T | c.930C>T | c.(928-930)gcC>gcT | p.A310A |
SKCM | 3 | 47036849 | 47036849 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr3:47036849G>T | c.1624G>T | c.(1624-1626)Gga>Tga | p.G542* |
SKCM | 3 | 47036850 | 47036850 | + | Missense_Mutation | SNP | G | G | A | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr3:47036850G>A | c.1625G>A | c.(1624-1626)gGa>gAa | p.G542E |
SKCM | 3 | 47036851 | 47036851 | + | Silent | SNP | A | A | T | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr3:47036851A>T | c.1626A>T | c.(1624-1626)ggA>ggT | p.G542G |
SKCM | 3 | 47037099 | 47037099 | + | Missense_Mutation | SNP | C | C | T | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr3:47037099C>T | c.1874C>T | c.(1873-1875)cCa>cTa | p.P625L |
SKCM | 3 | 47037254 | 47037254 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29M-06A-11D-A196-08 | TCGA-EE-A29M-10A-01D-A198-08 | g.chr3:47037254G>A | c.1949G>A | c.(1948-1950)gGg>gAg | p.G650E |
SKCM | 3 | 47038258 | 47038258 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MP-06A-11D-A197-08 | TCGA-EE-A2MP-10A-01D-A199-08 | g.chr3:47038258C>T | c.2491C>T | c.(2491-2493)Ccc>Tcc | p.P831S |
SKCM | 3 | 47039691 | 47039691 | + | Silent | SNP | C | C | T | TCGA-GF-A3OT-06A-23D-A23B-08 | TCGA-GF-A3OT-10A-01D-A23B-08 | g.chr3:47039691C>T | c.3093C>T | c.(3091-3093)acC>acT | p.T1031T |
SKCM | 3 | 47039692 | 47039692 | + | Missense_Mutation | SNP | C | C | T | TCGA-GF-A3OT-06A-23D-A23B-08 | TCGA-GF-A3OT-10A-01D-A23B-08 | g.chr3:47039692C>T | c.3094C>T | c.(3094-3096)Ctc>Ttc | p.L1032F |
SKCM | 3 | 47041163 | 47041163 | + | Silent | SNP | C | C | T | TCGA-D3-A5GR-06A-11D-A27K-08 | TCGA-D3-A5GR-10A-01D-A27N-08 | g.chr3:47041163C>T | c.3747C>T | c.(3745-3747)tcC>tcT | p.S1249S |
SKCM | 3 | 47041164 | 47041164 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr3:47041164C>T | c.3748C>T | c.(3748-3750)Ctc>Ttc | p.L1250F |
SKCM | 3 | 47041551 | 47041551 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr3:47041551C>T | c.3962C>T | c.(3961-3963)cCc>cTc | p.P1321L |
SKCM | 3 | 47042819 | 47042819 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3JA-06A-11D-A20D-08 | TCGA-EE-A3JA-10A-01D-A20D-08 | g.chr3:47042819C>T | c.4535C>T | c.(4534-4536)cCc>cTc | p.P1512L |
SKCM | 3 | 47042835 | 47042835 | + | Silent | SNP | C | C | T | TCGA-EE-A2M5-06A-12D-A197-08 | TCGA-EE-A2M5-10A-01D-A199-08 | g.chr3:47042835C>T | c.4551C>T | c.(4549-4551)gcC>gcT | p.A1517A |
SKCM | 3 | 47043209 | 47043209 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr3:47043209C>T | c.4675C>T | c.(4675-4677)Cgc>Tgc | p.R1559C |
SKCM | 3 | 47043253 | 47043253 | + | Silent | SNP | C | C | T | TCGA-GF-A6C9-06A-11D-A30X-08 | TCGA-GF-A6C9-10A-01D-A30X-08 | g.chr3:47043253C>T | c.4719C>T | c.(4717-4719)ctC>ctT | p.L1573L |
SKCM | 3 | 47043884 | 47043884 | + | Silent | SNP | C | C | T | TCGA-D9-A1JW-06A-11D-A19A-08 | TCGA-D9-A1JW-10A-01D-A19A-08 | g.chr3:47043884C>T | c.5175C>T | c.(5173-5175)ttC>ttT | p.F1725F |
SKCM | 3 | 47043884 | 47043884 | + | Silent | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr3:47043884C>T | c.5175C>T | c.(5173-5175)ttC>ttT | p.F1725F |
SKCM | 3 | 47043969 | 47043969 | + | Missense_Mutation | SNP | C | C | T | TCGA-EB-A44Q-06A-11D-A25O-08 | TCGA-EB-A44Q-10A-01D-A25O-08 | g.chr3:47043969C>T | c.5260C>T | c.(5260-5262)Cgg>Tgg | p.R1754W |
SKCM | 3 | 47044494 | 47044494 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr3:47044494C>T | c.5507C>T | c.(5506-5508)tCa>tTa | p.S1836L |
SKCM | 3 | 47045637 | 47045637 | + | Silent | SNP | C | C | T | TCGA-D3-A5GN-06A-11D-A27K-08 | TCGA-D3-A5GN-10A-01D-A27N-08 | g.chr3:47045637C>T | c.5952C>T | c.(5950-5952)cgC>cgT | p.R1984R |
SKCM | 3 | 47045731 | 47045731 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-EE-A3AC-06A-11D-A196-08 | TCGA-EE-A3AC-10A-01D-A198-08 | g.chr3:47045731C>T | c.6046C>T | c.(6046-6048)Cag>Tag | p.Q2016* |
SKCM | 3 | 47045759 | 47045759 | + | Missense_Mutation | SNP | T | T | C | TCGA-EB-A5UN-06A-11D-A30X-08 | TCGA-EB-A5UN-10A-01D-A30X-08 | g.chr3:47045759T>C | c.6074T>C | c.(6073-6075)aTc>aCc | p.I2025T |
SKCM | 3 | 47046037 | 47046037 | + | Missense_Mutation | SNP | C | C | T | TCGA-D9-A3Z1-06A-11D-A23B-08 | TCGA-D9-A3Z1-10A-01D-A23B-08 | g.chr3:47046037C>T | c.6251C>T | c.(6250-6252)aCc>aTc | p.T2084I |
SKCM | 3 | 47046714 | 47046714 | + | Missense_Mutation | SNP | C | C | T | TCGA-FS-A4FC-06A-11D-A24R-08 | TCGA-FS-A4FC-10A-01D-A24R-08 | g.chr3:47046714C>T | c.6463C>T | c.(6463-6465)Cac>Tac | p.H2155Y |
SKCM | 3 | 47047317 | 47047317 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-ER-A19W-06A-41D-A23B-08 | TCGA-ER-A19W-10A-01D-A23B-08 | g.chr3:47047317C>T | c.6781C>T | c.(6781-6783)Cag>Tag | p.Q2261* |
SKCM | 3 | 47049159 | 47049159 | + | Silent | SNP | G | G | A | TCGA-FS-A1ZZ-06A-11D-A197-08 | TCGA-FS-A1ZZ-10A-01D-A199-08 | g.chr3:47049159G>A | c.7479G>A | c.(7477-7479)aaG>aaA | p.K2493K |
SKCM | 3 | 47049364 | 47049364 | + | Silent | SNP | G | G | A | TCGA-D3-A3C3-06A-12D-A19A-08 | TCGA-D3-A3C3-10A-01D-A19A-08 | g.chr3:47049364G>A | c.7566G>A | c.(7564-7566)cgG>cgA | p.R2522R |
SKCM | 3 | 47049645 | 47049645 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A3J5-06A-11D-A20D-08 | TCGA-EE-A3J5-10A-01D-A20D-08 | g.chr3:47049645C>T | c.7688C>T | c.(7687-7689)aCt>aTt | p.T2563I |
SKCM | 3 | 47050061 | 47050061 | + | Silent | SNP | C | C | T | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr3:47050061C>T | c.7930C>T | c.(7930-7932)Ctg>Ttg | p.L2644L |
SKCM | 3 | 47050062 | 47050062 | + | Missense_Mutation | SNP | T | T | C | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr3:47050062T>C | c.7931T>C | c.(7930-7932)cTg>cCg | p.L2644P |