| 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 | 17 | 41234470 | 41234470 | + | Silent | SNP | A | A | G | TCGA-OR-A5J7-01A-11D-A29I-10 | TCGA-OR-A5J7-10A-01D-A29L-10 | g.chr17:41234470A>G | c.4308T>C | c.(4306-4308)tcT>tcC | p.S1436S |
| BLCA | 17 | 41203122 | 41203122 | + | Missense_Mutation | SNP | G | G | T | TCGA-K4-A3WS-01A-11D-A22Z-08 | TCGA-K4-A3WS-10A-01D-A22Z-08 | g.chr17:41203122G>T | c.5290C>A | c.(5290-5292)Cta>Ata | p.L1764I |
| BLCA | 17 | 41215352 | 41215352 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-XF-AAMX-01A-11D-A42E-08 | TCGA-XF-AAMX-10A-01D-A42H-08 | g.chr17:41215352C>A | c.5191G>T | c.(5191-5193)Gag>Tag | p.E1731* |
| BLCA | 17 | 41215388 | 41215388 | + | Missense_Mutation | SNP | C | C | T | TCGA-XF-A9T6-01A-11D-A42E-08 | TCGA-XF-A9T6-10A-01D-A42H-08 | g.chr17:41215388C>T | c.5155G>A | c.(5155-5157)Gtg>Atg | p.V1719M |
| BLCA | 17 | 41219632 | 41219632 | + | Missense_Mutation | SNP | C | C | T | TCGA-XF-AAMX-01A-11D-A42E-08 | TCGA-XF-AAMX-10A-01D-A42H-08 | g.chr17:41219632C>T | c.5067G>A | c.(5065-5067)atG>atA | p.M1689I |
| BLCA | 17 | 41223131 | 41223131 | + | Silent | SNP | C | C | T | TCGA-XF-AAMX-01A-11D-A42E-08 | TCGA-XF-AAMX-10A-01D-A42H-08 | g.chr17:41223131C>T | c.4800G>A | c.(4798-4800)ttG>ttA | p.L1600L |
| BLCA | 17 | 41223190 | 41223190 | + | Missense_Mutation | SNP | C | C | T | TCGA-XF-AAMX-01A-11D-A42E-08 | TCGA-XF-AAMX-10A-01D-A42H-08 | g.chr17:41223190C>T | c.4741G>A | c.(4741-4743)Gaa>Aaa | p.E1581K |
| BLCA | 17 | 41242998 | 41242998 | + | Nonsense_Mutation | SNP | G | G | C | TCGA-G2-AA3B-01A-11D-A391-08 | TCGA-G2-AA3B-10A-01D-A394-08 | g.chr17:41242998G>C | c.4148C>G | c.(4147-4149)tCa>tGa | p.S1383* |
| BLCA | 17 | 41243707 | 41243707 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-G2-A2EL-01A-12D-A18F-08 | TCGA-G2-A2EL-10A-01D-A18F-08 | g.chr17:41243707G>A | c.3841C>T | c.(3841-3843)Cag>Tag | p.Q1281* |
| BLCA | 17 | 41243920 | 41243920 | + | Missense_Mutation | SNP | C | C | G | TCGA-GU-AATQ-01A-11D-A391-08 | TCGA-GU-AATQ-10A-01D-A394-08 | g.chr17:41243920C>G | c.3628G>C | c.(3628-3630)Gag>Cag | p.E1210Q |
| BLCA | 17 | 41244457 | 41244457 | + | Missense_Mutation | SNP | T | T | C | TCGA-UY-A9PA-01A-11D-A38G-08 | TCGA-UY-A9PA-10A-01D-A38J-08 | g.chr17:41244457T>C | c.3091A>G | c.(3091-3093)Att>Gtt | p.I1031V |
| BLCA | 17 | 41244538 | 41244538 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-PQ-A6FN-01A-11D-A31L-08 | TCGA-PQ-A6FN-10A-01D-A31J-08 | g.chr17:41244538C>A | c.3010G>T | c.(3010-3012)Gag>Tag | p.E1004* |
| BLCA | 17 | 41244679 | 41244679 | + | Missense_Mutation | SNP | G | G | C | TCGA-ZF-A9RG-01A-21D-A42E-08 | TCGA-ZF-A9RG-10A-01D-A42H-08 | g.chr17:41244679G>C | c.2869C>G | c.(2869-2871)Cag>Gag | p.Q957E |
| BLCA | 17 | 41244840 | 41244840 | + | Missense_Mutation | SNP | C | C | G | TCGA-BT-A20W-01A-21D-A14W-08 | TCGA-BT-A20W-11A-11D-A14W-08 | g.chr17:41244840C>G | c.2708G>C | c.(2707-2709)tGt>tCt | p.C903S |
| BLCA | 17 | 41245222 | 41245222 | + | Missense_Mutation | SNP | C | C | A | TCGA-XF-AAMW-01A-11D-A42E-08 | TCGA-XF-AAMW-10A-01D-A42H-08 | g.chr17:41245222C>A | c.2326G>T | c.(2326-2328)Gat>Tat | p.D776Y |
| BLCA | 17 | 41245549 | 41245549 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-ZF-AA4W-01A-12D-A38G-08 | TCGA-ZF-AA4W-10A-01D-A38J-08 | g.chr17:41245549G>A | c.1999C>T | c.(1999-2001)Caa>Taa | p.Q667* |
| BLCA | 17 | 41245834 | 41245834 | + | Missense_Mutation | SNP | C | C | T | TCGA-BT-A3PH-01A-11D-A21Z-08 | TCGA-BT-A3PH-10A-01D-A21Z-08 | g.chr17:41245834C>T | c.1714G>A | c.(1714-1716)Gaa>Aaa | p.E572K |
| BLCA | 17 | 41245878 | 41245878 | + | Missense_Mutation | SNP | G | G | T | TCGA-XF-AAMR-01A-31D-A42E-08 | TCGA-XF-AAMR-10A-01D-A42H-08 | g.chr17:41245878G>T | c.1670C>A | c.(1669-1671)aCa>aAa | p.T557K |
| BLCA | 17 | 41246211 | 41246211 | + | Missense_Mutation | SNP | C | C | G | TCGA-DK-A1AE-01A-11D-A13W-08 | TCGA-DK-A1AE-10A-01D-A13W-08 | g.chr17:41246211C>G | c.1337G>C | c.(1336-1338)aGa>aCa | p.R446T |
| BLCA | 17 | 41246489 | 41246489 | + | Missense_Mutation | SNP | C | C | G | TCGA-GV-A6ZA-01A-12D-A339-08 | TCGA-GV-A6ZA-10A-01D-A339-08 | g.chr17:41246489C>G | c.1059G>C | c.(1057-1059)tgG>tgC | p.W353C |
| BLCA | 17 | 41246522 | 41246522 | + | Silent | SNP | C | C | G | TCGA-DK-A3IN-01A-11D-A20D-08 | TCGA-DK-A3IN-10A-01D-A20D-08 | g.chr17:41246522C>G | c.1026G>C | c.(1024-1026)ctG>ctC | p.L342L |
| BLCA | 17 | 41246641 | 41246641 | + | Missense_Mutation | SNP | C | C | T | TCGA-GV-A6ZA-01A-12D-A339-08 | TCGA-GV-A6ZA-10A-01D-A339-08 | g.chr17:41246641C>T | c.907G>A | c.(907-909)Gaa>Aaa | p.E303K |
| BLCA | 17 | 41246791 | 41246791 | + | Missense_Mutation | SNP | C | C | T | TCGA-4Z-AA89-01A-11D-A391-08 | TCGA-4Z-AA89-10A-01D-A394-08 | g.chr17:41246791C>T | c.757G>A | c.(757-759)Gca>Aca | p.A253T |
| BLCA | 17 | 41256936 | 41256936 | + | Missense_Mutation | SNP | C | C | T | TCGA-SY-A9G5-01A-11D-A38G-08 | TCGA-SY-A9G5-10A-01D-A38J-08 | g.chr17:41256936C>T | c.250G>A | c.(250-252)Gaa>Aaa | p.E84K |
| BLCA | 17 | 41267787 | 41267787 | + | Missense_Mutation | SNP | C | C | A | TCGA-XF-AAMG-01A-11D-A42E-08 | TCGA-XF-AAMG-10A-01D-A42H-08 | g.chr17:41267787C>A | c.90G>T | c.(88-90)ttG>ttT | p.L30F |
| BLCA | 17 | 41267787 | 41267787 | + | Missense_Mutation | SNP | C | C | G | TCGA-4Z-AA7R-01A-11D-A391-08 | TCGA-4Z-AA7R-10A-01D-A394-08 | g.chr17:41267787C>G | c.90G>C | c.(88-90)ttG>ttC | p.L30F |
| BRCA | 17 | 41201181 | 41201181 | + | Missense_Mutation | SNP | C | C | A | TCGA-AN-A0XU-01A-11D-A10G-09 | TCGA-AN-A0XU-10A-01D-A10G-09 | g.chr17:41201181C>A | c.5363G>T | c.(5362-5364)gGt>gTt | p.G1788V |
| BRCA | 17 | 41223090 | 41223090 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-D8-A27M-01A-11D-A16D-09 | TCGA-D8-A27M-10A-01D-A16D-09 | g.chr17:41223090delG | c.4841delC | c.(4840-4842)ccafs | p.P1614fs |
| BRCA | 17 | 41223256 | 41223256 | + | Splice_Site | SNP | C | C | T | TCGA-BH-A0WA-01A-11D-A10G-09 | TCGA-BH-A0WA-10A-01D-A117-09 | g.chr17:41223256C>T | | c.e15-1 | |
| BRCA | 17 | 41228540 | 41228540 | + | Silent | SNP | A | A | G | TCGA-AC-A5EH-01A-11D-A28B-09 | TCGA-AC-A5EH-10A-01D-A28E-09 | g.chr17:41228540A>G | c.4449T>C | c.(4447-4449)agT>agC | p.S1483S |
| BRCA | 17 | 41234523 | 41234523 | + | Missense_Mutation | SNP | C | C | T | TCGA-PE-A5DE-01A-11D-A27P-09 | TCGA-PE-A5DE-10A-01D-A27P-09 | g.chr17:41234523C>T | c.4255G>A | c.(4255-4257)Gaa>Aaa | p.E1419K |
| BRCA | 17 | 41243518 | 41243518 | + | Missense_Mutation | SNP | C | C | G | TCGA-C8-A12T-01A-11D-A10Y-09 | TCGA-C8-A12T-10A-01D-A110-09 | g.chr17:41243518C>G | c.4030G>C | c.(4030-4032)Gat>Cat | p.D1344H |
| BRCA | 17 | 41244296 | 41244296 | + | Silent | SNP | A | A | T | TCGA-E9-A54X-01A-11D-A25Q-09 | TCGA-E9-A54X-10A-01D-A25Q-09 | g.chr17:41244296A>T | c.3252T>A | c.(3250-3252)ctT>ctA | p.L1084L |
| BRCA | 17 | 41244468 | 41244468 | + | Missense_Mutation | SNP | C | C | A | TCGA-E2-A1L9-01A-11D-A13L-09 | TCGA-E2-A1L9-10A-01D-A188-09 | g.chr17:41244468C>A | c.3080G>T | c.(3079-3081)aGc>aTc | p.S1027I |
| BRCA | 17 | 41244479 | 41244479 | + | Silent | SNP | C | C | T | TCGA-LQ-A4E4-01A-11D-A25Q-09 | TCGA-LQ-A4E4-10A-01D-A25Q-09 | g.chr17:41244479C>T | c.3069G>A | c.(3067-3069)gtG>gtA | p.V1023V |
| BRCA | 17 | 41245390 | 41245390 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-A2-A25B-01A-11D-A167-09 | TCGA-A2-A25B-10A-01D-A167-09 | g.chr17:41245390C>A | c.2158G>T | c.(2158-2160)Gaa>Taa | p.E720* |
| BRCA | 17 | 41245615 | 41245617 | + | In_Frame_Del | DEL | AAC | AAC | - | TCGA-AO-A1KR-01A-12D-A142-09 | TCGA-AO-A1KR-10A-01D-A142-09 | g.chr17:41245615_41245617delAAC | c.1931_1933delGTT | c.(1930-1935)tgttct>tct | p.C644del |
| BRCA | 17 | 41245985 | 41245985 | + | Silent | SNP | T | T | C | TCGA-A1-A0SK-01A-12D-A099-09 | TCGA-A1-A0SK-10A-03D-A099-09 | g.chr17:41245985T>C | c.1563A>G | c.(1561-1563)gcA>gcG | p.A521A |
| BRCA | 17 | 41246452 | 41246452 | + | Missense_Mutation | SNP | C | C | T | TCGA-EW-A2FR-01A-11D-A21Q-09 | TCGA-EW-A2FR-10A-01D-A21Q-09 | g.chr17:41246452C>T | c.1096G>A | c.(1096-1098)Gat>Aat | p.D366N |
| BRCA | 17 | 41256165 | 41256165 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-E9-A1NC-01A-12W-A16L-09 | TCGA-E9-A1NC-10A-01D-A159-09 | g.chr17:41256165G>A | c.415C>T | c.(415-417)Cag>Tag | p.Q139* |
| BRCA | 17 | 41256900 | 41256900 | + | Missense_Mutation | SNP | C | C | G | TCGA-LL-A5YP-01A-21D-A28B-09 | TCGA-LL-A5YP-10A-01D-A28E-09 | g.chr17:41256900C>G | c.286G>C | c.(286-288)Gac>Cac | p.D96H |
| BRCA | 17 | 41258536 | 41258536 | + | Missense_Mutation | SNP | T | T | G | TCGA-A2-A4S0-01A-21D-A25Q-09 | TCGA-A2-A4S0-10A-01D-A25Q-09 | g.chr17:41258536T>G | c.149A>C | c.(148-150)aAa>aCa | p.K50T |
| BRCA | 17 | 41276089 | 41276089 | + | Missense_Mutation | SNP | C | C | G | TCGA-A1-A0SI-01A-11D-A142-09 | TCGA-A1-A0SI-10B-01D-A142-09 | g.chr17:41276089C>G | c.25G>C | c.(25-27)Gaa>Caa | p.E9Q |
| CESC | 17 | 41209115 | 41209115 | + | Missense_Mutation | SNP | C | C | T | TCGA-EK-A2PG-01A-11D-A18J-09 | TCGA-EK-A2PG-10A-01D-A18J-09 | g.chr17:41209115C>T | c.5231G>A | c.(5230-5232)aGa>aAa | p.R1744K |
| CESC | 17 | 41215378 | 41215378 | + | Missense_Mutation | SNP | G | G | A | TCGA-C5-A1BI-01B-11D-A13W-08 | TCGA-C5-A1BI-10A-01D-A13W-08 | g.chr17:41215378G>A | c.5165C>T | c.(5164-5166)tCt>tTt | p.S1722F |
| CESC | 17 | 41219655 | 41219655 | + | Missense_Mutation | SNP | C | C | T | TCGA-EK-A3GM-01A-11D-A20U-09 | TCGA-EK-A3GM-10A-01D-A20U-09 | g.chr17:41219655C>T | c.5044G>A | c.(5044-5046)Gaa>Aaa | p.E1682K |
| CESC | 17 | 41223131 | 41223131 | + | Silent | SNP | C | C | T | TCGA-LP-A4AV-01A-11D-A243-09 | TCGA-LP-A4AV-10A-01D-A243-09 | g.chr17:41223131C>T | c.4800G>A | c.(4798-4800)ttG>ttA | p.L1600L |
| CESC | 17 | 41226417 | 41226417 | + | Missense_Mutation | SNP | C | C | T | TCGA-DR-A0ZM-01A-12D-A10S-08 | TCGA-DR-A0ZM-10A-01D-A10S-08 | g.chr17:41226417C>T | c.4606G>A | c.(4606-4608)Gag>Aag | p.E1536K |
| CESC | 17 | 41246005 | 41246005 | + | Missense_Mutation | SNP | C | C | G | TCGA-EK-A3GK-01A-11D-A20U-09 | TCGA-EK-A3GK-10A-01D-A20U-09 | g.chr17:41246005C>G | c.1543G>C | c.(1543-1545)Gag>Cag | p.E515Q |
| CHOL | 17 | 41219699 | 41219699 | + | Missense_Mutation | SNP | T | T | G | TCGA-W5-AA2G-01A-11D-A417-09 | TCGA-W5-AA2G-10A-01D-A41A-09 | g.chr17:41219699T>G | c.5000A>C | c.(4999-5001)aAg>aCg | p.K1667T |
| COAD | 17 | 41197782 | 41197782 | + | Silent | SNP | T | T | C | TCGA-G4-6310-01A-11D-1719-10 | TCGA-G4-6310-10A-01D-1720-10 | g.chr17:41197782T>C | c.5505A>G | c.(5503-5505)cgA>cgG | p.R1835R |
| COAD | 17 | 41197783 | 41197783 | + | Missense_Mutation | SNP | C | C | A | TCGA-DM-A1HB-01A-21D-A183-10 | TCGA-DM-A1HB-10A-01D-A183-10 | g.chr17:41197783C>A | c.5504G>T | c.(5503-5505)cGa>cTa | p.R1835L |
| COAD | 17 | 41197784 | 41197784 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-CK-4952-01A-01D-1719-10 | TCGA-CK-4952-10A-01D-1719-10 | g.chr17:41197784G>A | c.5503C>T | c.(5503-5505)Cga>Tga | p.R1835* |
| COAD | 17 | 41197784 | 41197784 | + | Silent | SNP | G | G | T | TCGA-DM-A28G-01A-11D-A16V-10 | TCGA-DM-A28G-10A-01D-A16V-10 | g.chr17:41197784G>T | c.5503C>A | c.(5503-5505)Cga>Aga | p.R1835R |
| COAD | 17 | 41209068 | 41209068 | + | Splice_Site | SNP | C | C | A | TCGA-AD-6889-01A-11D-1924-10 | TCGA-AD-6889-10A-01D-1924-10 | g.chr17:41209068C>A | | c.e19+1 | |
| COAD | 17 | 41209093 | 41209093 | + | Silent | SNP | T | T | C | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr17:41209093T>C | c.5253A>G | c.(5251-5253)cgA>cgG | p.R1751R |
| COAD | 17 | 41209093 | 41209093 | + | Silent | SNP | T | T | C | TCGA-AZ-6607-01A-11D-1835-10 | TCGA-AZ-6607-11A-01D-1835-10 | g.chr17:41209093T>C | c.5253A>G | c.(5251-5253)cgA>cgG | p.R1751R |
| COAD | 17 | 41215369 | 41215369 | + | Missense_Mutation | SNP | T | T | C | TCGA-G4-6317-01A-11D-1719-10 | TCGA-G4-6317-10A-01D-1720-10 | g.chr17:41215369T>C | c.5174A>G | c.(5173-5175)gAa>gGa | p.E1725G |
| COAD | 17 | 41215925 | 41215925 | + | Silent | SNP | T | T | C | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr17:41215925T>C | c.5118A>G | c.(5116-5118)ggA>ggG | p.G1706G |
| COAD | 17 | 41223038 | 41223038 | + | Silent | SNP | A | A | G | TCGA-DM-A1HB-01A-21D-A183-10 | TCGA-DM-A1HB-10A-01D-A183-10 | g.chr17:41223038A>G | c.4893T>C | c.(4891-4893)agT>agC | p.S1631S |
| COAD | 17 | 41226409 | 41226409 | + | Silent | SNP | C | C | T | TCGA-AA-3697-01A-01D-1719-10 | TCGA-AA-3697-11A-01D-1719-10 | g.chr17:41226409C>T | c.4614G>A | c.(4612-4614)caG>caA | p.Q1538Q |
| COAD | 17 | 41226515 | 41226515 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr17:41226515G>T | c.4508C>A | c.(4507-4509)tCa>tAa | p.S1503* |
| COAD | 17 | 41234476 | 41234476 | + | Silent | SNP | A | A | G | TCGA-A6-6780-01A-11D-1835-10 | TCGA-A6-6780-10A-01D-1835-10 | g.chr17:41234476A>G | c.4302T>C | c.(4300-4302)agT>agC | p.S1434S |
| COAD | 17 | 41243595 | 41243595 | + | Missense_Mutation | SNP | A | A | G | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr17:41243595A>G | c.3953T>C | c.(3952-3954)aTt>aCt | p.I1318T |
| COAD | 17 | 41243774 | 41243774 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3510-01A-01D-1408-10 | TCGA-AA-3510-11A-01D-1408-10 | g.chr17:41243774C>A | c.3774G>T | c.(3772-3774)gaG>gaT | p.E1258D |
| COAD | 17 | 41243809 | 41243809 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3492-01A-01D-1408-10 | TCGA-AA-3492-11A-01D-1408-10 | g.chr17:41243809C>T | c.3739G>A | c.(3739-3741)Gtt>Att | p.V1247I |
| COAD | 17 | 41244128 | 41244128 | + | Silent | SNP | A | A | G | TCGA-D5-5540-01A-01D-1650-10 | TCGA-D5-5540-10A-01D-1650-10 | g.chr17:41244128A>G | c.3420T>C | c.(3418-3420)agT>agC | p.S1140S |
| COAD | 17 | 41244128 | 41244128 | + | Silent | SNP | A | A | G | TCGA-F4-6808-01A-11D-1835-10 | TCGA-F4-6808-10A-01D-1835-10 | g.chr17:41244128A>G | c.3420T>C | c.(3418-3420)agT>agC | p.S1140S |
| COAD | 17 | 41244317 | 41244317 | + | Silent | SNP | C | C | T | TCGA-CM-6680-01A-11D-1835-10 | TCGA-CM-6680-10A-01D-1835-10 | g.chr17:41244317C>T | c.3231G>A | c.(3229-3231)ggG>ggA | p.G1077G |
| COAD | 17 | 41244521 | 41244521 | + | Silent | SNP | T | T | C | TCGA-AZ-6603-01A-11D-1835-10 | TCGA-AZ-6603-11A-02D-1835-10 | g.chr17:41244521T>C | c.3027A>G | c.(3025-3027)tcA>tcG | p.S1009S |
| COAD | 17 | 41244521 | 41244521 | + | Silent | SNP | T | T | C | TCGA-D5-6898-01A-11D-1924-10 | TCGA-D5-6898-10A-01D-1924-10 | g.chr17:41244521T>C | c.3027A>G | c.(3025-3027)tcA>tcG | p.S1009S |
| COAD | 17 | 41244523 | 41244523 | + | Missense_Mutation | SNP | A | A | G | TCGA-A6-6782-01A-11D-1835-10 | TCGA-A6-6782-10A-01D-1835-10 | g.chr17:41244523A>G | c.3025T>C | c.(3025-3027)Tca>Cca | p.S1009P |
| COAD | 17 | 41244523 | 41244523 | + | Missense_Mutation | SNP | A | A | G | TCGA-CK-4948-01B-11D-1650-10 | TCGA-CK-4948-10A-01D-1650-10 | g.chr17:41244523A>G | c.3025T>C | c.(3025-3027)Tca>Cca | p.S1009P |
| COAD | 17 | 41244523 | 41244523 | + | Missense_Mutation | SNP | A | A | G | TCGA-D5-5537-01A-21D-1924-10 | TCGA-D5-5537-10A-01D-1924-10 | g.chr17:41244523A>G | c.3025T>C | c.(3025-3027)Tca>Cca | p.S1009P |
| COAD | 17 | 41244523 | 41244523 | + | Missense_Mutation | SNP | A | A | G | TCGA-D5-6928-01A-11D-1924-10 | TCGA-D5-6928-10A-01D-1924-10 | g.chr17:41244523A>G | c.3025T>C | c.(3025-3027)Tca>Cca | p.S1009P |
| COAD | 17 | 41244829 | 41244829 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr17:41244829C>T | c.2719G>A | c.(2719-2721)Gaa>Aaa | p.E907K |
| COAD | 17 | 41245087 | 41245087 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr17:41245087C>A | c.2461G>T | c.(2461-2463)Gat>Tat | p.D821Y |
| COAD | 17 | 41245107 | 41245107 | + | Missense_Mutation | SNP | A | A | G | TCGA-CM-5864-01A-01D-1650-10 | TCGA-CM-5864-10A-01D-1650-10 | g.chr17:41245107A>G | c.2441T>C | c.(2440-2442)cTa>cCa | p.L814P |
| COAD | 17 | 41245214 | 41245214 | + | Silent | SNP | G | G | T | TCGA-G4-6626-01A-11D-1771-10 | TCGA-G4-6626-10A-01D-1771-10 | g.chr17:41245214G>T | c.2334C>A | c.(2332-2334)ggC>ggA | p.G778G |
| COAD | 17 | 41245274 | 41245274 | + | Silent | SNP | C | C | T | TCGA-AD-6963-01A-11D-1924-10 | TCGA-AD-6963-10A-01D-1924-10 | g.chr17:41245274C>T | c.2274G>A | c.(2272-2274)ttG>ttA | p.L758L |
| COAD | 17 | 41245274 | 41245274 | + | Silent | SNP | C | C | T | TCGA-CK-6748-01A-11D-1835-10 | TCGA-CK-6748-10A-01D-1835-10 | g.chr17:41245274C>T | c.2274G>A | c.(2272-2274)ttG>ttA | p.L758L |
| COAD | 17 | 41245274 | 41245274 | + | Silent | SNP | C | C | T | TCGA-DM-A0X9-01A-11D-A152-10 | TCGA-DM-A0X9-10A-01D-A152-10 | g.chr17:41245274C>T | c.2274G>A | c.(2272-2274)ttG>ttA | p.L758L |
| COAD | 17 | 41245276 | 41245276 | + | Silent | SNP | A | A | G | TCGA-D5-6920-01A-11D-1924-10 | TCGA-D5-6920-10A-01D-1924-10 | g.chr17:41245276A>G | c.2272T>C | c.(2272-2274)Ttg>Ctg | p.L758L |
| COAD | 17 | 41245332 | 41245333 | + | Frame_Shift_Ins | INS | - | - | TA | TCGA-F4-6570-01A-11D-1771-10 | TCGA-F4-6570-10A-01D-1771-10 | g.chr17:41245332_41245333insTA | c.2215_2216insTA | c.(2215-2217)aaafs | p.K739fs |
| COAD | 17 | 41245479 | 41245479 | + | Missense_Mutation | SNP | T | T | C | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr17:41245479T>C | c.2069A>G | c.(2068-2070)aAa>aGa | p.K690R |
| COAD | 17 | 41245586 | 41245587 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-A6-3809-01A-01W-0995-10 | TCGA-A6-3809-11A-01W-0995-10 | g.chr17:41245586_41245587insT | c.1961_1962insA | c.(1960-1962)aagfs | p.K654fs |
| COAD | 17 | 41246082 | 41246082 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3715-01A-01W-0900-09 | TCGA-AA-3715-10A-01W-0900-09 | g.chr17:41246082T>C | c.1466A>G | c.(1465-1467)gAg>gGg | p.E489G |
| COAD | 17 | 41246195 | 41246195 | + | Silent | SNP | T | T | C | TCGA-A6-5659-01A-01D-1650-10 | TCGA-A6-5659-11A-01D-1650-10 | g.chr17:41246195T>C | c.1353A>G | c.(1351-1353)tcA>tcG | p.S451S |
| COAD | 17 | 41246195 | 41246195 | + | Silent | SNP | T | T | C | TCGA-D5-5540-01A-01D-1650-10 | TCGA-D5-5540-10A-01D-1650-10 | g.chr17:41246195T>C | c.1353A>G | c.(1351-1353)tcA>tcG | p.S451S |
| COAD | 17 | 41246255 | 41246255 | + | Silent | SNP | T | T | C | TCGA-CK-6747-01A-11D-1835-10 | TCGA-CK-6747-10A-01D-1835-10 | g.chr17:41246255T>C | c.1293A>G | c.(1291-1293)ttA>ttG | p.L431L |
| COAD | 17 | 41246255 | 41246255 | + | Silent | SNP | T | T | C | TCGA-G4-6586-01A-11D-1771-10 | TCGA-G4-6586-10A-01D-1771-10 | g.chr17:41246255T>C | c.1293A>G | c.(1291-1293)ttA>ttG | p.L431L |
| COAD | 17 | 41246432 | 41246432 | + | Missense_Mutation | SNP | C | C | A | TCGA-AZ-6599-01A-11D-1771-10 | TCGA-AZ-6599-11A-01D-1771-10 | g.chr17:41246432C>A | c.1116G>T | c.(1114-1116)tgG>tgT | p.W372C |
| COAD | 17 | 41247864 | 41247864 | + | Splice_Site | SNP | C | C | G | TCGA-CA-5797-01A-01D-1650-10 | TCGA-CA-5797-10A-01D-1650-10 | g.chr17:41247864C>G | c.669G>C | c.(667-669)aaG>aaC | p.K223N |
| COAD | 17 | 41251830 | 41251830 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A00E-01A-01W-A005-10 | TCGA-AA-A00E-10A-01W-A005-10 | g.chr17:41251830C>T | c.509G>A | c.(508-510)cGg>cAg | p.R170Q |
| COAD | 17 | 41256232 | 41256232 | + | Silent | SNP | T | T | C | TCGA-DM-A28C-01A-11D-A16V-10 | TCGA-DM-A28C-10A-01D-A16V-10 | g.chr17:41256232T>C | c.348A>G | c.(346-348)gaA>gaG | p.E116E |
| COAD | 17 | 41256232 | 41256232 | + | Silent | SNP | T | T | C | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr17:41256232T>C | c.348A>G | c.(346-348)gaA>gaG | p.E116E |
| COAD | 17 | 41256234 | 41256234 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3496-01A-21D-1835-10 | TCGA-AA-3496-11A-01D-1835-10 | g.chr17:41256234C>T | c.346G>A | c.(346-348)Gaa>Aaa | p.E116K |
| COAD | 17 | 41256238 | 41256238 | + | Silent | SNP | A | A | G | TCGA-A6-5660-01A-01D-1650-10 | TCGA-A6-5660-10A-01D-1650-10 | g.chr17:41256238A>G | c.342T>C | c.(340-342)tcT>tcC | p.S114S |
| COAD | 17 | 41256238 | 41256238 | + | Silent | SNP | A | A | G | TCGA-AA-3697-01A-01D-1719-10 | TCGA-AA-3697-11A-01D-1719-10 | g.chr17:41256238A>G | c.342T>C | c.(340-342)tcT>tcC | p.S114S |
| COAD | 17 | 41256238 | 41256238 | + | Silent | SNP | A | A | G | TCGA-AA-3968-01A-01W-0995-10 | TCGA-AA-3968-10A-01W-0995-10 | g.chr17:41256238A>G | c.342T>C | c.(340-342)tcT>tcC | p.S114S |
| COAD | 17 | 41256238 | 41256238 | + | Silent | SNP | A | A | G | TCGA-CM-6164-01A-11D-1650-10 | TCGA-CM-6164-10A-01D-1650-10 | g.chr17:41256238A>G | c.342T>C | c.(340-342)tcT>tcC | p.S114S |
| COAD | 17 | 41256238 | 41256238 | + | Silent | SNP | A | A | G | TCGA-D5-6931-01A-11D-1924-10 | TCGA-D5-6931-10A-01D-1924-10 | g.chr17:41256238A>G | c.342T>C | c.(340-342)tcT>tcC | p.S114S |
| COAD | 17 | 41256238 | 41256238 | + | Silent | SNP | A | A | G | TCGA-DM-A1HA-01A-11D-A152-10 | TCGA-DM-A1HA-10A-01D-A152-10 | g.chr17:41256238A>G | c.342T>C | c.(340-342)tcT>tcC | p.S114S |
| COAD | 17 | 41256240 | 41256240 | + | Missense_Mutation | SNP | A | A | G | TCGA-CM-5862-01A-01D-1650-10 | TCGA-CM-5862-10A-01D-1650-10 | g.chr17:41256240A>G | c.340T>C | c.(340-342)Tct>Cct | p.S114P |
| COAD | 17 | 41256240 | 41256240 | + | Missense_Mutation | SNP | A | A | G | TCGA-DM-A1D6-01A-21D-A152-10 | TCGA-DM-A1D6-10A-01D-A152-10 | g.chr17:41256240A>G | c.340T>C | c.(340-342)Tct>Cct | p.S114P |
| COAD | 17 | 41256251 | 41256251 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-CM-6171-01A-11D-1650-10 | TCGA-CM-6171-10A-01D-1650-10 | g.chr17:41256251delT | c.329delA | c.(328-330)aagfs | p.K110fs |
| COAD | 17 | 41258514 | 41258514 | + | Silent | SNP | C | C | T | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr17:41258514C>T | c.171G>A | c.(169-171)ggG>ggA | p.G57G |
| COAD | 17 | 41258544 | 41258544 | + | Silent | SNP | G | G | A | TCGA-CK-5914-01A-11D-1650-10 | TCGA-CK-5914-10A-01D-1650-10 | g.chr17:41258544G>A | c.141C>T | c.(139-141)tgC>tgT | p.C47C |
| COAD | 17 | 41258546 | 41258546 | + | Missense_Mutation | SNP | A | A | G | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr17:41258546A>G | c.139T>C | c.(139-141)Tgc>Cgc | p.C47R |
| COAD | 17 | 41276093 | 41276093 | + | Silent | SNP | G | G | A | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr17:41276093G>A | c.21C>T | c.(19-21)cgC>cgT | p.R7R |
| COADREAD | 17 | 41197782 | 41197782 | + | Silent | SNP | T | T | C | TCGA-EI-6507-01A-11D-1733-10 | TCGA-EI-6507-10A-01D-1733-10 | g.chr17:41197782T>C | c.5505A>G | c.(5503-5505)cgA>cgG | p.R1835R |
| COADREAD | 17 | 41197782 | 41197782 | + | Silent | SNP | T | T | C | TCGA-G4-6310-01A-11D-1719-10 | TCGA-G4-6310-10A-01D-1720-10 | g.chr17:41197782T>C | c.5505A>G | c.(5503-5505)cgA>cgG | p.R1835R |
| COADREAD | 17 | 41197783 | 41197783 | + | Missense_Mutation | SNP | C | C | A | TCGA-DM-A1HB-01A-21D-A183-10 | TCGA-DM-A1HB-10A-01D-A183-10 | g.chr17:41197783C>A | c.5504G>T | c.(5503-5505)cGa>cTa | p.R1835L |
| COADREAD | 17 | 41197783 | 41197783 | + | Missense_Mutation | SNP | C | C | A | TCGA-EI-6506-01A-11D-1733-10 | TCGA-EI-6506-10A-01D-1733-10 | g.chr17:41197783C>A | c.5504G>T | c.(5503-5505)cGa>cTa | p.R1835L |
| COADREAD | 17 | 41197784 | 41197784 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-CK-4952-01A-01D-1719-10 | TCGA-CK-4952-10A-01D-1719-10 | g.chr17:41197784G>A | c.5503C>T | c.(5503-5505)Cga>Tga | p.R1835* |
| COADREAD | 17 | 41197784 | 41197784 | + | Silent | SNP | G | G | T | TCGA-DM-A28G-01A-11D-A16V-10 | TCGA-DM-A28G-10A-01D-A16V-10 | g.chr17:41197784G>T | c.5503C>A | c.(5503-5505)Cga>Aga | p.R1835R |
| COADREAD | 17 | 41209068 | 41209068 | + | Splice_Site | SNP | C | C | A | TCGA-AD-6889-01A-11D-1924-10 | TCGA-AD-6889-10A-01D-1924-10 | g.chr17:41209068C>A | | c.e19+1 | |
| COADREAD | 17 | 41209093 | 41209093 | + | Silent | SNP | T | T | C | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr17:41209093T>C | c.5253A>G | c.(5251-5253)cgA>cgG | p.R1751R |
| COADREAD | 17 | 41209093 | 41209093 | + | Silent | SNP | T | T | C | TCGA-AZ-6607-01A-11D-1835-10 | TCGA-AZ-6607-11A-01D-1835-10 | g.chr17:41209093T>C | c.5253A>G | c.(5251-5253)cgA>cgG | p.R1751R |
| COADREAD | 17 | 41215369 | 41215369 | + | Missense_Mutation | SNP | T | T | C | TCGA-G4-6317-01A-11D-1719-10 | TCGA-G4-6317-10A-01D-1720-10 | g.chr17:41215369T>C | c.5174A>G | c.(5173-5175)gAa>gGa | p.E1725G |
| COADREAD | 17 | 41215925 | 41215925 | + | Silent | SNP | T | T | C | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr17:41215925T>C | c.5118A>G | c.(5116-5118)ggA>ggG | p.G1706G |
| COADREAD | 17 | 41223038 | 41223038 | + | Silent | SNP | A | A | G | TCGA-DM-A1HB-01A-21D-A183-10 | TCGA-DM-A1HB-10A-01D-A183-10 | g.chr17:41223038A>G | c.4893T>C | c.(4891-4893)agT>agC | p.S1631S |
| COADREAD | 17 | 41226409 | 41226409 | + | Silent | SNP | C | C | T | TCGA-AA-3697-01A-01D-1719-10 | TCGA-AA-3697-11A-01D-1719-10 | g.chr17:41226409C>T | c.4614G>A | c.(4612-4614)caG>caA | p.Q1538Q |
| COADREAD | 17 | 41226515 | 41226515 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chr17:41226515G>T | c.4508C>A | c.(4507-4509)tCa>tAa | p.S1503* |
| COADREAD | 17 | 41234476 | 41234476 | + | Silent | SNP | A | A | G | TCGA-A6-6780-01A-11D-1835-10 | TCGA-A6-6780-10A-01D-1835-10 | g.chr17:41234476A>G | c.4302T>C | c.(4300-4302)agT>agC | p.S1434S |
| COADREAD | 17 | 41243595 | 41243595 | + | Missense_Mutation | SNP | A | A | G | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr17:41243595A>G | c.3953T>C | c.(3952-3954)aTt>aCt | p.I1318T |
| COADREAD | 17 | 41243774 | 41243774 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3510-01A-01D-1408-10 | TCGA-AA-3510-11A-01D-1408-10 | g.chr17:41243774C>A | c.3774G>T | c.(3772-3774)gaG>gaT | p.E1258D |
| COADREAD | 17 | 41243809 | 41243809 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3492-01A-01D-1408-10 | TCGA-AA-3492-11A-01D-1408-10 | g.chr17:41243809C>T | c.3739G>A | c.(3739-3741)Gtt>Att | p.V1247I |
| COADREAD | 17 | 41244128 | 41244128 | + | Silent | SNP | A | A | G | TCGA-D5-5540-01A-01D-1650-10 | TCGA-D5-5540-10A-01D-1650-10 | g.chr17:41244128A>G | c.3420T>C | c.(3418-3420)agT>agC | p.S1140S |
| COADREAD | 17 | 41244128 | 41244128 | + | Silent | SNP | A | A | G | TCGA-F4-6808-01A-11D-1835-10 | TCGA-F4-6808-10A-01D-1835-10 | g.chr17:41244128A>G | c.3420T>C | c.(3418-3420)agT>agC | p.S1140S |
| COADREAD | 17 | 41244317 | 41244317 | + | Silent | SNP | C | C | T | TCGA-CM-6680-01A-11D-1835-10 | TCGA-CM-6680-10A-01D-1835-10 | g.chr17:41244317C>T | c.3231G>A | c.(3229-3231)ggG>ggA | p.G1077G |
| COADREAD | 17 | 41244521 | 41244521 | + | Silent | SNP | T | T | C | TCGA-AZ-6603-01A-11D-1835-10 | TCGA-AZ-6603-11A-02D-1835-10 | g.chr17:41244521T>C | c.3027A>G | c.(3025-3027)tcA>tcG | p.S1009S |
| COADREAD | 17 | 41244521 | 41244521 | + | Silent | SNP | T | T | C | TCGA-D5-6898-01A-11D-1924-10 | TCGA-D5-6898-10A-01D-1924-10 | g.chr17:41244521T>C | c.3027A>G | c.(3025-3027)tcA>tcG | p.S1009S |
| COADREAD | 17 | 41244523 | 41244523 | + | Missense_Mutation | SNP | A | A | G | TCGA-A6-6782-01A-11D-1835-10 | TCGA-A6-6782-10A-01D-1835-10 | g.chr17:41244523A>G | c.3025T>C | c.(3025-3027)Tca>Cca | p.S1009P |
| COADREAD | 17 | 41244523 | 41244523 | + | Missense_Mutation | SNP | A | A | G | TCGA-CI-6619-01B-11D-1826-10 | TCGA-CI-6619-10A-01D-1826-10 | g.chr17:41244523A>G | c.3025T>C | c.(3025-3027)Tca>Cca | p.S1009P |
| COADREAD | 17 | 41244523 | 41244523 | + | Missense_Mutation | SNP | A | A | G | TCGA-CK-4948-01B-11D-1650-10 | TCGA-CK-4948-10A-01D-1650-10 | g.chr17:41244523A>G | c.3025T>C | c.(3025-3027)Tca>Cca | p.S1009P |
| COADREAD | 17 | 41244523 | 41244523 | + | Missense_Mutation | SNP | A | A | G | TCGA-D5-5537-01A-21D-1924-10 | TCGA-D5-5537-10A-01D-1924-10 | g.chr17:41244523A>G | c.3025T>C | c.(3025-3027)Tca>Cca | p.S1009P |
| COADREAD | 17 | 41244523 | 41244523 | + | Missense_Mutation | SNP | A | A | G | TCGA-D5-6928-01A-11D-1924-10 | TCGA-D5-6928-10A-01D-1924-10 | g.chr17:41244523A>G | c.3025T>C | c.(3025-3027)Tca>Cca | p.S1009P |
| COADREAD | 17 | 41244829 | 41244829 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr17:41244829C>T | c.2719G>A | c.(2719-2721)Gaa>Aaa | p.E907K |
| COADREAD | 17 | 41245087 | 41245087 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr17:41245087C>A | c.2461G>T | c.(2461-2463)Gat>Tat | p.D821Y |
| COADREAD | 17 | 41245107 | 41245107 | + | Missense_Mutation | SNP | A | A | G | TCGA-CM-5864-01A-01D-1650-10 | TCGA-CM-5864-10A-01D-1650-10 | g.chr17:41245107A>G | c.2441T>C | c.(2440-2442)cTa>cCa | p.L814P |
| COADREAD | 17 | 41245214 | 41245214 | + | Silent | SNP | G | G | T | TCGA-G4-6626-01A-11D-1771-10 | TCGA-G4-6626-10A-01D-1771-10 | g.chr17:41245214G>T | c.2334C>A | c.(2332-2334)ggC>ggA | p.G778G |
| COADREAD | 17 | 41245274 | 41245274 | + | Silent | SNP | C | C | T | TCGA-AD-6963-01A-11D-1924-10 | TCGA-AD-6963-10A-01D-1924-10 | g.chr17:41245274C>T | c.2274G>A | c.(2272-2274)ttG>ttA | p.L758L |
| COADREAD | 17 | 41245274 | 41245274 | + | Silent | SNP | C | C | T | TCGA-CK-6748-01A-11D-1835-10 | TCGA-CK-6748-10A-01D-1835-10 | g.chr17:41245274C>T | c.2274G>A | c.(2272-2274)ttG>ttA | p.L758L |
| COADREAD | 17 | 41245274 | 41245274 | + | Silent | SNP | C | C | T | TCGA-DM-A0X9-01A-11D-A152-10 | TCGA-DM-A0X9-10A-01D-A152-10 | g.chr17:41245274C>T | c.2274G>A | c.(2272-2274)ttG>ttA | p.L758L |
| COADREAD | 17 | 41245276 | 41245276 | + | Silent | SNP | A | A | G | TCGA-D5-6920-01A-11D-1924-10 | TCGA-D5-6920-10A-01D-1924-10 | g.chr17:41245276A>G | c.2272T>C | c.(2272-2274)Ttg>Ctg | p.L758L |
| COADREAD | 17 | 41245332 | 41245333 | + | Frame_Shift_Ins | INS | - | - | TA | TCGA-F4-6570-01A-11D-1771-10 | TCGA-F4-6570-10A-01D-1771-10 | g.chr17:41245332_41245333insTA | c.2215_2216insTA | c.(2215-2217)aaafs | p.K739fs |
| COADREAD | 17 | 41245479 | 41245479 | + | Missense_Mutation | SNP | T | T | C | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr17:41245479T>C | c.2069A>G | c.(2068-2070)aAa>aGa | p.K690R |
| COADREAD | 17 | 41245586 | 41245587 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-A6-3809-01A-01W-0995-10 | TCGA-A6-3809-11A-01W-0995-10 | g.chr17:41245586_41245587insT | c.1961_1962insA | c.(1960-1962)aagfs | p.K654fs |
| COADREAD | 17 | 41246082 | 41246082 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3715-01A-01W-0900-09 | TCGA-AA-3715-10A-01W-0900-09 | g.chr17:41246082T>C | c.1466A>G | c.(1465-1467)gAg>gGg | p.E489G |
| COADREAD | 17 | 41246189 | 41246189 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr17:41246189C>A | c.1359G>T | c.(1357-1359)gaG>gaT | p.E453D |
| COADREAD | 17 | 41246195 | 41246195 | + | Silent | SNP | T | T | C | TCGA-A6-5659-01A-01D-1650-10 | TCGA-A6-5659-11A-01D-1650-10 | g.chr17:41246195T>C | c.1353A>G | c.(1351-1353)tcA>tcG | p.S451S |
| COADREAD | 17 | 41246195 | 41246195 | + | Silent | SNP | T | T | C | TCGA-D5-5540-01A-01D-1650-10 | TCGA-D5-5540-10A-01D-1650-10 | g.chr17:41246195T>C | c.1353A>G | c.(1351-1353)tcA>tcG | p.S451S |
| COADREAD | 17 | 41246255 | 41246255 | + | Silent | SNP | T | T | C | TCGA-CK-6747-01A-11D-1835-10 | TCGA-CK-6747-10A-01D-1835-10 | g.chr17:41246255T>C | c.1293A>G | c.(1291-1293)ttA>ttG | p.L431L |
| COADREAD | 17 | 41246255 | 41246255 | + | Silent | SNP | T | T | C | TCGA-G4-6586-01A-11D-1771-10 | TCGA-G4-6586-10A-01D-1771-10 | g.chr17:41246255T>C | c.1293A>G | c.(1291-1293)ttA>ttG | p.L431L |
| COADREAD | 17 | 41246432 | 41246432 | + | Missense_Mutation | SNP | C | C | A | TCGA-AZ-6599-01A-11D-1771-10 | TCGA-AZ-6599-11A-01D-1771-10 | g.chr17:41246432C>A | c.1116G>T | c.(1114-1116)tgG>tgT | p.W372C |
| COADREAD | 17 | 41247864 | 41247864 | + | Splice_Site | SNP | C | C | G | TCGA-CA-5797-01A-01D-1650-10 | TCGA-CA-5797-10A-01D-1650-10 | g.chr17:41247864C>G | c.669G>C | c.(667-669)aaG>aaC | p.K223N |
| COADREAD | 17 | 41251830 | 41251830 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A00E-01A-01W-A005-10 | TCGA-AA-A00E-10A-01W-A005-10 | g.chr17:41251830C>T | c.509G>A | c.(508-510)cGg>cAg | p.R170Q |
| COADREAD | 17 | 41256232 | 41256232 | + | Silent | SNP | T | T | C | TCGA-DM-A28C-01A-11D-A16V-10 | TCGA-DM-A28C-10A-01D-A16V-10 | g.chr17:41256232T>C | c.348A>G | c.(346-348)gaA>gaG | p.E116E |
| COADREAD | 17 | 41256232 | 41256232 | + | Silent | SNP | T | T | C | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr17:41256232T>C | c.348A>G | c.(346-348)gaA>gaG | p.E116E |
| COADREAD | 17 | 41256234 | 41256234 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3496-01A-21D-1835-10 | TCGA-AA-3496-11A-01D-1835-10 | g.chr17:41256234C>T | c.346G>A | c.(346-348)Gaa>Aaa | p.E116K |
| COADREAD | 17 | 41256238 | 41256238 | + | Silent | SNP | A | A | G | TCGA-A6-5660-01A-01D-1650-10 | TCGA-A6-5660-10A-01D-1650-10 | g.chr17:41256238A>G | c.342T>C | c.(340-342)tcT>tcC | p.S114S |
| COADREAD | 17 | 41256238 | 41256238 | + | Silent | SNP | A | A | G | TCGA-AA-3697-01A-01D-1719-10 | TCGA-AA-3697-11A-01D-1719-10 | g.chr17:41256238A>G | c.342T>C | c.(340-342)tcT>tcC | p.S114S |
| COADREAD | 17 | 41256238 | 41256238 | + | Silent | SNP | A | A | G | TCGA-AA-3968-01A-01W-0995-10 | TCGA-AA-3968-10A-01W-0995-10 | g.chr17:41256238A>G | c.342T>C | c.(340-342)tcT>tcC | p.S114S |
| COADREAD | 17 | 41256238 | 41256238 | + | Silent | SNP | A | A | G | TCGA-CM-6164-01A-11D-1650-10 | TCGA-CM-6164-10A-01D-1650-10 | g.chr17:41256238A>G | c.342T>C | c.(340-342)tcT>tcC | p.S114S |
| COADREAD | 17 | 41256238 | 41256238 | + | Silent | SNP | A | A | G | TCGA-D5-6931-01A-11D-1924-10 | TCGA-D5-6931-10A-01D-1924-10 | g.chr17:41256238A>G | c.342T>C | c.(340-342)tcT>tcC | p.S114S |
| COADREAD | 17 | 41256238 | 41256238 | + | Silent | SNP | A | A | G | TCGA-DM-A1HA-01A-11D-A152-10 | TCGA-DM-A1HA-10A-01D-A152-10 | g.chr17:41256238A>G | c.342T>C | c.(340-342)tcT>tcC | p.S114S |
| COADREAD | 17 | 41256240 | 41256240 | + | Missense_Mutation | SNP | A | A | G | TCGA-CM-5862-01A-01D-1650-10 | TCGA-CM-5862-10A-01D-1650-10 | g.chr17:41256240A>G | c.340T>C | c.(340-342)Tct>Cct | p.S114P |
| COADREAD | 17 | 41256240 | 41256240 | + | Missense_Mutation | SNP | A | A | G | TCGA-DM-A1D6-01A-21D-A152-10 | TCGA-DM-A1D6-10A-01D-A152-10 | g.chr17:41256240A>G | c.340T>C | c.(340-342)Tct>Cct | p.S114P |
| COADREAD | 17 | 41256251 | 41256251 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-CM-6171-01A-11D-1650-10 | TCGA-CM-6171-10A-01D-1650-10 | g.chr17:41256251delT | c.329delA | c.(328-330)aagfs | p.K110fs |
| COADREAD | 17 | 41258514 | 41258514 | + | Silent | SNP | C | C | T | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr17:41258514C>T | c.171G>A | c.(169-171)ggG>ggA | p.G57G |
| COADREAD | 17 | 41258544 | 41258544 | + | Silent | SNP | G | G | A | TCGA-CK-5914-01A-11D-1650-10 | TCGA-CK-5914-10A-01D-1650-10 | g.chr17:41258544G>A | c.141C>T | c.(139-141)tgC>tgT | p.C47C |
| COADREAD | 17 | 41258546 | 41258546 | + | Missense_Mutation | SNP | A | A | G | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr17:41258546A>G | c.139T>C | c.(139-141)Tgc>Cgc | p.C47R |
| COADREAD | 17 | 41276093 | 41276093 | + | Silent | SNP | G | G | A | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr17:41276093G>A | c.21C>T | c.(19-21)cgC>cgT | p.R7R |
| DLBC | 17 | 41234477 | 41234477 | + | Missense_Mutation | SNP | C | C | T | TCGA-GS-A9TY-01A-11D-A38X-10 | TCGA-GS-A9TY-10A-01D-A38X-10 | g.chr17:41234477C>T | c.4301G>A | c.(4300-4302)aGt>aAt | p.S1434N |
| DLBC | 17 | 41245531 | 41245531 | + | Missense_Mutation | SNP | C | C | T | TCGA-GS-A9TZ-01A-11D-A38X-10 | TCGA-GS-A9TZ-10A-01D-A38X-10 | g.chr17:41245531C>T | c.2017G>A | c.(2017-2019)Gaa>Aaa | p.E673K |
| DLBC | 17 | 41245643 | 41245643 | + | Silent | SNP | A | A | G | TCGA-G8-6324-01A-11D-2210-10 | TCGA-G8-6324-10A-01D-2210-10 | g.chr17:41245643A>G | c.1905T>C | c.(1903-1905)aaT>aaC | p.N635N |
| ESCA | 17 | 41203114 | 41203114 | + | Silent | SNP | G | G | T | TCGA-L5-A8NI-01A-11D-A37C-09 | TCGA-L5-A8NI-11A-11D-A37F-09 | g.chr17:41203114G>T | c.5298C>A | c.(5296-5298)atC>atA | p.I1766I |
| ESCA | 17 | 41219693 | 41219693 | + | Missense_Mutation | SNP | G | G | T | TCGA-LN-A9FR-01A-11D-A387-09 | TCGA-LN-A9FR-10A-01D-A38A-09 | g.chr17:41219693G>T | c.5006C>A | c.(5005-5007)gCc>gAc | p.A1669D |
| ESCA | 17 | 41223241 | 41223241 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-X8-AAAR-01A-11D-A403-09 | TCGA-X8-AAAR-10A-01D-A403-09 | g.chr17:41223241delG | c.4690delC | c.(4690-4692)ctgfs | p.L1564fs |
| ESCA | 17 | 41234517 | 41234517 | + | Missense_Mutation | SNP | G | G | T | TCGA-KH-A6WC-01A-11D-A33E-09 | TCGA-KH-A6WC-10B-01D-A33H-09 | g.chr17:41234517G>T | c.4261C>A | c.(4261-4263)Cat>Aat | p.H1421N |
| ESCA | 17 | 41244511 | 41244511 | + | Missense_Mutation | SNP | C | C | G | TCGA-L5-A8NS-01A-12D-A37C-09 | TCGA-L5-A8NS-11A-11D-A37F-09 | g.chr17:41244511C>G | c.3037G>C | c.(3037-3039)Gaa>Caa | p.E1013Q |
| ESCA | 17 | 41245977 | 41245977 | + | Missense_Mutation | SNP | G | G | T | TCGA-R6-A6Y2-01B-11D-A33E-09 | TCGA-R6-A6Y2-10A-01D-A33H-09 | g.chr17:41245977G>T | c.1571C>A | c.(1570-1572)gCa>gAa | p.A524E |
| ESCA | 17 | 41247865 | 41247865 | + | Missense_Mutation | SNP | T | T | G | TCGA-LN-A9FP-01A-31D-A387-09 | TCGA-LN-A9FP-10A-01D-A38A-09 | g.chr17:41247865T>G | c.668A>C | c.(667-669)aAg>aCg | p.K223T |
| ESCA | 17 | 41276051 | 41276051 | + | Silent | SNP | G | G | A | TCGA-2H-A9GF-01A-11D-A37C-09 | TCGA-2H-A9GF-11A-11D-A37F-09 | g.chr17:41276051G>A | c.63C>T | c.(61-63)atC>atT | p.I21I |
| GBM | 17 | 41243940 | 41243940 | + | Missense_Mutation | SNP | C | C | T | TCGA-06-5858-01A-01D-1696-08 | TCGA-06-5858-10A-01D-1696-08 | g.chr17:41243940C>T | c.3608G>A | c.(3607-3609)cGa>cAa | p.R1203Q |
| GBM | 17 | 41244603 | 41244603 | + | Missense_Mutation | SNP | G | G | A | TCGA-06-0649-01B-01W-0348-08 | TCGA-06-0649-10A-01W-0348-08 | g.chr17:41244603G>A | c.2945C>T | c.(2944-2946)cCa>cTa | p.P982L |
| GBM | 17 | 41244612 | 41244612 | + | Missense_Mutation | SNP | C | C | T | TCGA-76-4927-01A-01D-1486-08 | TCGA-76-4927-10A-01D-1486-08 | g.chr17:41244612C>T | c.2936G>A | c.(2935-2937)cGt>cAt | p.R979H |
| GBM | 17 | 41245683 | 41245683 | + | Missense_Mutation | SNP | G | G | A | TCGA-41-2575-01A-01D-1495-08 | TCGA-41-2575-10A-01D-1495-08 | g.chr17:41245683G>A | c.1865C>T | c.(1864-1866)gCg>gTg | p.A622V |
| GBMLGG | 17 | 41201147 | 41201147 | + | Silent | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr17:41201147G>T | c.5397C>A | c.(5395-5397)acC>acA | p.T1799T |
| GBMLGG | 17 | 41243940 | 41243940 | + | Missense_Mutation | SNP | C | C | T | TCGA-06-5858-01A-01D-1696-08 | TCGA-06-5858-10A-01D-1696-08 | g.chr17:41243940C>T | c.3608G>A | c.(3607-3609)cGa>cAa | p.R1203Q |
| GBMLGG | 17 | 41244542 | 41244542 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr17:41244542G>T | c.3006C>A | c.(3004-3006)aaC>aaA | p.N1002K |
| GBMLGG | 17 | 41244603 | 41244603 | + | Missense_Mutation | SNP | G | G | A | TCGA-06-0649-01B-01W-0348-08 | TCGA-06-0649-10A-01W-0348-08 | g.chr17:41244603G>A | c.2945C>T | c.(2944-2946)cCa>cTa | p.P982L |
| GBMLGG | 17 | 41244612 | 41244612 | + | Missense_Mutation | SNP | C | C | T | TCGA-76-4927-01A-01D-1486-08 | TCGA-76-4927-10A-01D-1486-08 | g.chr17:41244612C>T | c.2936G>A | c.(2935-2937)cGt>cAt | p.R979H |
| GBMLGG | 17 | 41244758 | 41244758 | + | Silent | SNP | A | A | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr17:41244758A>G | c.2790T>C | c.(2788-2790)ccT>ccC | p.P930P |
| GBMLGG | 17 | 41245683 | 41245683 | + | Missense_Mutation | SNP | G | G | A | TCGA-41-2575-01A-01D-1495-08 | TCGA-41-2575-10A-01D-1495-08 | g.chr17:41245683G>A | c.1865C>T | c.(1864-1866)gCg>gTg | p.A622V |
| GBMLGG | 17 | 41276094 | 41276094 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-A76K-01A-11D-A33T-08 | TCGA-DU-A76K-10A-01D-A33W-08 | g.chr17:41276094C>T | c.20G>A | c.(19-21)cGc>cAc | p.R7H |
| HNSC | 17 | 41209136 | 41209136 | + | Missense_Mutation | SNP | C | C | G | TCGA-F7-A50J-01A-21D-A28R-08 | TCGA-F7-A50J-10A-01D-A28U-08 | g.chr17:41209136C>G | c.5210G>C | c.(5209-5211)aGa>aCa | p.R1737T |
| HNSC | 17 | 41222997 | 41222997 | + | Missense_Mutation | SNP | C | C | A | TCGA-CV-7250-01A-11D-2012-08 | TCGA-CV-7250-10A-01D-2013-08 | g.chr17:41222997C>A | c.4934G>T | c.(4933-4935)aGg>aTg | p.R1645M |
| HNSC | 17 | 41226510 | 41226510 | + | Missense_Mutation | SNP | C | C | T | TCGA-CV-7245-01A-11D-2012-08 | TCGA-CV-7245-10A-01D-2013-08 | g.chr17:41226510C>T | c.4513G>A | c.(4513-4515)Gat>Aat | p.D1505N |
| HNSC | 17 | 41228515 | 41228515 | + | Missense_Mutation | SNP | C | C | T | TCGA-CV-7097-01A-11D-2012-08 | TCGA-CV-7097-10A-01D-2013-08 | g.chr17:41228515C>T | c.4474G>A | c.(4474-4476)Gga>Aga | p.G1492R |
| HNSC | 17 | 41243826 | 41243826 | + | Missense_Mutation | SNP | G | G | A | TCGA-CR-7404-01A-11D-2129-08 | TCGA-CR-7404-10A-01D-2129-08 | g.chr17:41243826G>A | c.3722C>T | c.(3721-3723)tCt>tTt | p.S1241F |
| HNSC | 17 | 41244991 | 41244991 | + | Missense_Mutation | SNP | C | C | T | TCGA-BA-6872-01A-11D-1870-08 | TCGA-BA-6872-10A-01D-1870-08 | g.chr17:41244991C>T | c.2557G>A | c.(2557-2559)Gat>Aat | p.D853N |
| HNSC | 17 | 41245102 | 41245102 | + | Missense_Mutation | SNP | G | G | A | TCGA-CR-7404-01A-11D-2129-08 | TCGA-CR-7404-10A-01D-2129-08 | g.chr17:41245102G>A | c.2446C>T | c.(2446-2448)Cat>Tat | p.H816Y |
| HNSC | 17 | 41245558 | 41245558 | + | Missense_Mutation | SNP | T | T | C | TCGA-CV-7248-01A-11D-2012-08 | TCGA-CV-7248-10A-01D-2013-08 | g.chr17:41245558T>C | c.1990A>G | c.(1990-1992)Aga>Gga | p.R664G |
| HNSC | 17 | 41246660 | 41246660 | + | Silent | SNP | T | T | C | TCGA-CN-5363-01A-01D-1434-08 | TCGA-CN-5363-10A-01D-1434-08 | g.chr17:41246660T>C | c.888A>G | c.(886-888)agA>agG | p.R296R |
| HNSC | 17 | 41246860 | 41246860 | + | Missense_Mutation | SNP | C | C | G | TCGA-CV-7099-01A-41D-2012-08 | TCGA-CV-7099-10A-01D-2013-08 | g.chr17:41246860C>G | c.688G>C | c.(688-690)Gag>Cag | p.E230Q |
| HNSC | 17 | 41249303 | 41249303 | + | Missense_Mutation | SNP | G | G | C | TCGA-CN-A6V1-01A-12D-A34J-08 | TCGA-CN-A6V1-10B-01D-A34M-08 | g.chr17:41249303G>C | c.551C>G | c.(550-552)tCt>tGt | p.S184C |
| HNSC | 17 | 41251814 | 41251814 | + | Missense_Mutation | SNP | C | C | G | TCGA-CV-A6K2-01A-11D-A31L-08 | TCGA-CV-A6K2-10A-01D-A31J-08 | g.chr17:41251814C>G | c.525G>C | c.(523-525)aaG>aaC | p.K175N |
| HNSC | 17 | 41256883 | 41256883 | + | Splice_Site | SNP | A | A | C | TCGA-D6-6823-01A-11D-1912-08 | TCGA-D6-6823-10A-01D-1912-08 | g.chr17:41256883A>C | | c.e5+1 | |
| HNSC | 17 | 41256889 | 41256889 | + | Silent | SNP | C | C | T | TCGA-CQ-5326-01A-01D-1870-08 | TCGA-CQ-5326-10A-01D-1870-08 | g.chr17:41256889C>T | c.297G>A | c.(295-297)ttG>ttA | p.L99L |
| HNSC | 17 | 41276072 | 41276072 | + | Silent | SNP | G | G | A | TCGA-CV-7424-01A-11D-2078-08 | TCGA-CV-7424-10A-01D-2078-08 | g.chr17:41276072G>A | c.42C>T | c.(40-42)gtC>gtT | p.V14V |
| KICH | 17 | 41244425 | 41244425 | + | Silent | SNP | T | T | C | TCGA-KN-8435-01A-11D-2310-10 | TCGA-KN-8435-11A-01D-2311-10 | g.chr17:41244425T>C | c.3123A>G | c.(3121-3123)tcA>tcG | p.S1041S |
| KIPAN | 17 | 41197795 | 41197795 | + | Missense_Mutation | SNP | G | G | A | TCGA-BP-4998-01A-01D-1462-08 | TCGA-BP-4998-11A-01D-1462-08 | g.chr17:41197795G>A | c.5492C>T | c.(5491-5493)cCt>cTt | p.P1831L |
| KIPAN | 17 | 41203099 | 41203099 | + | Silent | SNP | G | G | A | TCGA-B1-A655-01A-11D-A31Z-10 | TCGA-B1-A655-10A-01D-A31X-10 | g.chr17:41203099G>A | c.5313C>T | c.(5311-5313)ccC>ccT | p.P1771P |
| KIPAN | 17 | 41234582 | 41234582 | + | Missense_Mutation | SNP | G | G | C | TCGA-CJ-4643-01A-02D-1386-10 | TCGA-CJ-4643-11A-01D-1251-10 | g.chr17:41234582G>C | c.4196C>G | c.(4195-4197)aCc>aGc | p.T1399S |
| KIPAN | 17 | 41243622 | 41243623 | + | Missense_Mutation | DNP | TT | TT | AG | TCGA-CZ-4853-01A-01D-1429-08 | TCGA-CZ-4853-11A-01D-1429-08 | g.chr17:41243622_41243623TT>AG | c.3925_3926AA>CT | c.(3925-3927)AAt>CTt | p.N1309L |
| KIPAN | 17 | 41243848 | 41243848 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-SX-A71S-01A-11D-A33Q-10 | TCGA-SX-A71S-10A-01D-A33Q-10 | g.chr17:41243848delC | c.3700delG | c.(3700-3702)gtafs | p.V1234fs |
| KIPAN | 17 | 41244425 | 41244425 | + | Silent | SNP | T | T | C | TCGA-KN-8435-01A-11D-2310-10 | TCGA-KN-8435-11A-01D-2311-10 | g.chr17:41244425T>C | c.3123A>G | c.(3121-3123)tcA>tcG | p.S1041S |
| KIPAN | 17 | 41244817 | 41244817 | + | Missense_Mutation | SNP | C | C | T | TCGA-G7-6796-01A-11D-1961-08 | TCGA-G7-6796-10A-01D-1962-08 | g.chr17:41244817C>T | c.2731G>A | c.(2731-2733)Gga>Aga | p.G911R |
| KIPAN | 17 | 41246841 | 41246841 | + | Missense_Mutation | SNP | G | G | C | TCGA-5P-A9KC-01A-11D-A42J-10 | TCGA-5P-A9KC-10A-01D-A42M-10 | g.chr17:41246841G>C | c.707C>G | c.(706-708)aCt>aGt | p.T236S |
| KIPAN | 17 | 41267787 | 41267787 | + | Missense_Mutation | SNP | C | C | A | TCGA-BP-4160-01A-02D-1366-10 | TCGA-BP-4160-11A-01D-1806-10 | g.chr17:41267787C>A | c.90G>T | c.(88-90)ttG>ttT | p.L30F |
| KIRC | 17 | 41197795 | 41197795 | + | Missense_Mutation | SNP | G | G | A | TCGA-BP-4998-01A-01D-1462-08 | TCGA-BP-4998-11A-01D-1462-08 | g.chr17:41197795G>A | c.5492C>T | c.(5491-5493)cCt>cTt | p.P1831L |
| KIRC | 17 | 41234582 | 41234582 | + | Missense_Mutation | SNP | G | G | C | TCGA-CJ-4643-01A-02D-1386-10 | TCGA-CJ-4643-11A-01D-1251-10 | g.chr17:41234582G>C | c.4196C>G | c.(4195-4197)aCc>aGc | p.T1399S |
| KIRC | 17 | 41243622 | 41243623 | + | Missense_Mutation | DNP | TT | TT | AG | TCGA-CZ-4853-01A-01D-1429-08 | TCGA-CZ-4853-11A-01D-1429-08 | g.chr17:41243622_41243623TT>AG | c.3925_3926AA>CT | c.(3925-3927)AAt>CTt | p.N1309L |
| KIRC | 17 | 41267787 | 41267787 | + | Missense_Mutation | SNP | C | C | A | TCGA-BP-4160-01A-02D-1366-10 | TCGA-BP-4160-11A-01D-1806-10 | g.chr17:41267787C>A | c.90G>T | c.(88-90)ttG>ttT | p.L30F |
| KIRP | 17 | 41203099 | 41203099 | + | Silent | SNP | G | G | A | TCGA-B1-A655-01A-11D-A31Z-10 | TCGA-B1-A655-10A-01D-A31X-10 | g.chr17:41203099G>A | c.5313C>T | c.(5311-5313)ccC>ccT | p.P1771P |
| KIRP | 17 | 41243848 | 41243848 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-SX-A71S-01A-11D-A33Q-10 | TCGA-SX-A71S-10A-01D-A33Q-10 | g.chr17:41243848delC | c.3700delG | c.(3700-3702)gtafs | p.V1234fs |
| KIRP | 17 | 41244817 | 41244817 | + | Missense_Mutation | SNP | C | C | T | TCGA-G7-6796-01A-11D-1961-08 | TCGA-G7-6796-10A-01D-1962-08 | g.chr17:41244817C>T | c.2731G>A | c.(2731-2733)Gga>Aga | p.G911R |
| KIRP | 17 | 41246841 | 41246841 | + | Missense_Mutation | SNP | G | G | C | TCGA-5P-A9KC-01A-11D-A42J-10 | TCGA-5P-A9KC-10A-01D-A42M-10 | g.chr17:41246841G>C | c.707C>G | c.(706-708)aCt>aGt | p.T236S |
| LGG | 17 | 41201147 | 41201147 | + | Silent | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr17:41201147G>T | c.5397C>A | c.(5395-5397)acC>acA | p.T1799T |
| LGG | 17 | 41244542 | 41244542 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr17:41244542G>T | c.3006C>A | c.(3004-3006)aaC>aaA | p.N1002K |
| LGG | 17 | 41244758 | 41244758 | + | Silent | SNP | A | A | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr17:41244758A>G | c.2790T>C | c.(2788-2790)ccT>ccC | p.P930P |
| LGG | 17 | 41276094 | 41276094 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-A76K-01A-11D-A33T-08 | TCGA-DU-A76K-10A-01D-A33W-08 | g.chr17:41276094C>T | c.20G>A | c.(19-21)cGc>cAc | p.R7H |
| LIHC | 17 | 41203109 | 41203109 | + | Missense_Mutation | SNP | C | C | T | TCGA-DD-A39V-01A-11D-A20W-10 | TCGA-DD-A39V-11A-11D-A20W-10 | g.chr17:41203109C>T | c.5303G>A | c.(5302-5304)tGc>tAc | p.C1768Y |
| LIHC | 17 | 41219686 | 41219686 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-G3-A3CJ-01A-11D-A20W-10 | TCGA-G3-A3CJ-10A-01D-A20W-10 | g.chr17:41219686delT | c.5013delA | c.(5011-5013)aaafs | p.K1671fs |
| LIHC | 17 | 41223109 | 41223109 | + | Missense_Mutation | SNP | C | C | T | TCGA-BC-A112-01A-11D-A12Z-10 | TCGA-BC-A112-11A-11D-A12Z-10 | g.chr17:41223109C>T | c.4822G>A | c.(4822-4824)Gca>Aca | p.A1608T |
| LIHC | 17 | 41228506 | 41228506 | + | Splice_Site | SNP | T | T | C | TCGA-DD-A1ED-01A-11D-A152-10 | TCGA-DD-A1ED-10A-01D-A152-10 | g.chr17:41228506T>C | c.4483A>G | c.(4483-4485)Agg>Ggg | p.R1495G |
| LIHC | 17 | 41228578 | 41228578 | + | Missense_Mutation | SNP | C | C | G | TCGA-FV-A23B-01A-11D-A16V-10 | TCGA-FV-A23B-11A-11D-A16V-10 | g.chr17:41228578C>G | c.4411G>C | c.(4411-4413)Ggc>Cgc | p.G1471R |
| LIHC | 17 | 41245524 | 41245524 | + | Missense_Mutation | SNP | G | G | C | TCGA-DD-AAD1-01A-11D-A40R-10 | TCGA-DD-AAD1-10A-01D-A40U-10 | g.chr17:41245524G>C | c.2024C>G | c.(2023-2025)gCa>gGa | p.A675G |
| LIHC | 17 | 41245576 | 41245576 | + | Missense_Mutation | SNP | T | T | C | TCGA-DD-AAVZ-01A-11D-A40R-10 | TCGA-DD-AAVZ-10A-01D-A40U-10 | g.chr17:41245576T>C | c.1972A>G | c.(1972-1974)Atg>Gtg | p.M658V |
| LIHC | 17 | 41245778 | 41245778 | + | Silent | SNP | A | A | G | TCGA-G3-A7M7-01A-12D-A34Z-10 | TCGA-G3-A7M7-10A-01D-A34Z-10 | g.chr17:41245778A>G | c.1770T>C | c.(1768-1770)agT>agC | p.S590S |
| LIHC | 17 | 41246557 | 41246557 | + | Missense_Mutation | SNP | T | T | C | TCGA-ES-A2HT-01A-12D-A183-10 | TCGA-ES-A2HT-11A-11D-A183-10 | g.chr17:41246557T>C | c.991A>G | c.(991-993)Agg>Ggg | p.R331G |
| LIHC | 17 | 41246777 | 41246777 | + | Silent | SNP | A | A | G | TCGA-5C-A9VH-01A-11D-A36X-10 | TCGA-5C-A9VH-10A-01D-A370-10 | g.chr17:41246777A>G | c.771T>C | c.(769-771)caT>caC | p.H257H |
| LIHC | 17 | 41251836 | 41251836 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-G3-A3CJ-01A-11D-A20W-10 | TCGA-G3-A3CJ-10A-01D-A20W-10 | g.chr17:41251836delT | c.503delA | c.(502-504)aagfs | p.K168fs |
| LIHC | 17 | 41276097 | 41276097 | + | Missense_Mutation | SNP | A | A | G | TCGA-BC-A3KG-01A-11D-A20W-10 | TCGA-BC-A3KG-10A-01D-A20W-10 | g.chr17:41276097A>G | c.17T>C | c.(16-18)cTt>cCt | p.L6P |
| LUAD | 17 | 41199690 | 41199690 | + | Missense_Mutation | SNP | C | C | G | TCGA-17-Z026-01A-01W-0746-08 | TCGA-17-Z026-11A-01W-0746-08 | g.chr17:41199690C>G | c.5437G>C | c.(5437-5439)Gat>Cat | p.D1813H |
| LUAD | 17 | 41209101 | 41209101 | + | Missense_Mutation | SNP | G | G | A | TCGA-55-7281-01A-11D-2036-08 | TCGA-55-7281-10A-01D-2036-08 | g.chr17:41209101G>A | c.5245C>T | c.(5245-5247)Cca>Tca | p.P1749S |
| LUAD | 17 | 41219652 | 41219652 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-55-8208-01A-11D-2238-08 | TCGA-55-8208-10A-01D-2238-08 | g.chr17:41219652C>A | c.5047G>T | c.(5047-5049)Gag>Tag | p.E1683* |
| LUAD | 17 | 41219655 | 41219655 | + | Missense_Mutation | SNP | C | C | T | TCGA-55-8208-01A-11D-2238-08 | TCGA-55-8208-10A-01D-2238-08 | g.chr17:41219655C>T | c.5044G>A | c.(5044-5046)Gaa>Aaa | p.E1682K |
| LUAD | 17 | 41222985 | 41222985 | + | Missense_Mutation | SNP | C | C | G | TCGA-91-8499-01A-11D-2393-08 | TCGA-91-8499-10A-01D-2393-08 | g.chr17:41222985C>G | c.4946G>C | c.(4945-4947)aGa>aCa | p.R1649T |
| LUAD | 17 | 41222993 | 41222993 | + | Silent | SNP | G | G | A | TCGA-93-A4JP-01A-11D-A24P-08 | TCGA-93-A4JP-10A-01D-A24P-08 | g.chr17:41222993G>A | c.4938C>T | c.(4936-4938)gtC>gtT | p.V1646V |
| LUAD | 17 | 41222996 | 41222996 | + | Missense_Mutation | SNP | C | C | A | TCGA-MP-A4TK-01A-11D-A24P-08 | TCGA-MP-A4TK-10A-01D-A24P-08 | g.chr17:41222996C>A | c.4935G>T | c.(4933-4935)agG>agT | p.R1645S |
| LUAD | 17 | 41226380 | 41226380 | + | Missense_Mutation | SNP | G | G | A | TCGA-55-6972-01A-11D-1945-08 | TCGA-55-6972-11A-01D-1945-08 | g.chr17:41226380G>A | c.4643C>T | c.(4642-4644)aCg>aTg | p.T1548M |
| LUAD | 17 | 41226442 | 41226442 | + | Missense_Mutation | SNP | C | C | A | TCGA-44-8119-01A-11D-2238-08 | TCGA-44-8119-10A-01D-2238-08 | g.chr17:41226442C>A | c.4581G>T | c.(4579-4581)gaG>gaT | p.E1527D |
| LUAD | 17 | 41234512 | 41234512 | + | Silent | SNP | C | C | A | TCGA-97-7554-01A-11D-2036-08 | TCGA-97-7554-10A-01D-2036-08 | g.chr17:41234512C>A | c.4266G>T | c.(4264-4266)ggG>ggT | p.G1422G |
| LUAD | 17 | 41234513 | 41234513 | + | Missense_Mutation | SNP | C | C | A | TCGA-97-7554-01A-11D-2036-08 | TCGA-97-7554-10A-01D-2036-08 | g.chr17:41234513C>A | c.4265G>T | c.(4264-4266)gGg>gTg | p.G1422V |
| LUAD | 17 | 41243499 | 41243499 | + | Missense_Mutation | SNP | C | C | G | TCGA-05-4424-01A-22D-1855-08 | TCGA-05-4424-10A-01D-1855-08 | g.chr17:41243499C>G | c.4049G>C | c.(4048-4050)gGc>gCc | p.G1350A |
| LUAD | 17 | 41243619 | 41243619 | + | Missense_Mutation | SNP | G | G | A | TCGA-MP-A4TF-01A-11D-A25L-08 | TCGA-MP-A4TF-10A-01D-A25L-08 | g.chr17:41243619G>A | c.3929C>T | c.(3928-3930)aCa>aTa | p.T1310I |
| LUAD | 17 | 41243708 | 41243708 | + | Silent | SNP | A | A | G | TCGA-MN-A4N1-01A-11D-A24P-08 | TCGA-MN-A4N1-10A-01D-A24P-08 | g.chr17:41243708A>G | c.3840T>C | c.(3838-3840)tcT>tcC | p.S1280S |
| LUAD | 17 | 41243908 | 41243908 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-55-8620-01A-11D-2393-08 | TCGA-55-8620-10A-01D-2393-08 | g.chr17:41243908C>A | c.3640G>T | c.(3640-3642)Gag>Tag | p.E1214* |
| LUAD | 17 | 41244214 | 41244214 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-17-Z042-01A-01W-0746-08 | TCGA-17-Z042-11A-01W-0746-08 | g.chr17:41244214C>A | c.3334G>T | c.(3334-3336)Gaa>Taa | p.E1112* |
| LUAD | 17 | 41244550 | 41244550 | + | Missense_Mutation | SNP | C | C | G | TCGA-44-3396-01A-01D-1553-08 | TCGA-44-3396-10A-01D-1265-08 | g.chr17:41244550C>G | c.2998G>C | c.(2998-3000)Gag>Cag | p.E1000Q |
| LUAD | 17 | 41245429 | 41245429 | + | Missense_Mutation | SNP | C | C | G | TCGA-NJ-A4YF-01A-12D-A25L-08 | TCGA-NJ-A4YF-10A-01D-A25L-08 | g.chr17:41245429C>G | c.2119G>C | c.(2119-2121)Ggt>Cgt | p.G707R |
| LUAD | 17 | 41245544 | 41245544 | + | Silent | SNP | G | G | A | TCGA-05-5420-01A-01D-1625-08 | TCGA-05-5420-11A-01D-1625-08 | g.chr17:41245544G>A | c.2004C>T | c.(2002-2004)ctC>ctT | p.L668L |
| LUAD | 17 | 41245945 | 41245945 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-44-8117-01A-11D-2238-08 | TCGA-44-8117-10A-01D-2238-08 | g.chr17:41245945C>A | c.1603G>T | c.(1603-1605)Gga>Tga | p.G535* |
| LUAD | 17 | 41246294 | 41246294 | + | Missense_Mutation | SNP | C | C | G | TCGA-55-7570-01A-11D-2036-08 | TCGA-55-7570-10A-01D-2036-08 | g.chr17:41246294C>G | c.1254G>C | c.(1252-1254)gaG>gaC | p.E418D |
| LUAD | 17 | 41246314 | 41246314 | + | Missense_Mutation | SNP | C | C | A | TCGA-05-4382-01A-01D-1931-08 | TCGA-05-4382-10A-01D-1265-08 | g.chr17:41246314C>A | c.1234G>T | c.(1234-1236)Gta>Tta | p.V412L |
| LUAD | 17 | 41246510 | 41246510 | + | Silent | SNP | G | G | T | TCGA-55-7994-01A-11D-2184-08 | TCGA-55-7994-10A-01D-2184-08 | g.chr17:41246510G>T | c.1038C>A | c.(1036-1038)ccC>ccA | p.P346P |
| LUAD | 17 | 41251814 | 41251814 | + | Missense_Mutation | SNP | C | C | A | TCGA-50-6593-01A-11D-1753-08 | TCGA-50-6593-11A-01D-1753-08 | g.chr17:41251814C>A | c.525G>T | c.(523-525)aaG>aaT | p.K175N |
| LUAD | 17 | 41251869 | 41251869 | + | Missense_Mutation | SNP | G | G | C | TCGA-62-8394-01A-11D-2323-08 | TCGA-62-8394-10A-01D-2323-08 | g.chr17:41251869G>C | c.470C>G | c.(469-471)tCt>tGt | p.S157C |
| LUAD | 17 | 41256153 | 41256153 | + | Missense_Mutation | SNP | C | C | G | TCGA-80-5611-01A-01D-1625-08 | TCGA-80-5611-10A-01D-1625-08 | g.chr17:41256153C>G | c.427G>C | c.(427-429)Gaa>Caa | p.E143Q |
| LUAD | 17 | 41258529 | 41258529 | + | Silent | SNP | G | G | T | TCGA-78-7539-01A-11D-2063-08 | TCGA-78-7539-10A-01D-2063-08 | g.chr17:41258529G>T | c.156C>A | c.(154-156)ctC>ctA | p.L52L |
| LUAD | 17 | 41258541 | 41258541 | + | Missense_Mutation | SNP | C | C | G | TCGA-NJ-A4YQ-01A-11D-A25L-08 | TCGA-NJ-A4YQ-10A-01D-A25L-08 | g.chr17:41258541C>G | c.144G>C | c.(142-144)atG>atC | p.M48I |
| LUSC | 17 | 41215391 | 41215391 | + | Splice_Site | SNP | C | C | T | TCGA-43-5668-01A-01D-1632-08 | TCGA-43-5668-11A-01D-1632-08 | g.chr17:41215391C>T | | c.e18-1 | |
| LUSC | 17 | 41219706 | 41219706 | + | Missense_Mutation | SNP | C | C | A | TCGA-22-4613-01A-01D-1441-08 | TCGA-22-4613-11A-01D-1441-08 | g.chr17:41219706C>A | c.4993G>T | c.(4993-4995)Gtg>Ttg | p.V1665L |
| LUSC | 17 | 41243518 | 41243518 | + | Missense_Mutation | SNP | C | C | T | TCGA-34-2600-01A-01D-1522-08 | TCGA-34-2600-11A-01D-1522-08 | g.chr17:41243518C>T | c.4030G>A | c.(4030-4032)Gat>Aat | p.D1344N |
| LUSC | 17 | 41244070 | 41244070 | + | Nonsense_Mutation | SNP | T | T | A | TCGA-46-3769-01A-01D-0983-08 | TCGA-46-3769-10A-01D-0983-08 | g.chr17:41244070T>A | c.3478A>T | c.(3478-3480)Aag>Tag | p.K1160* |
| LUSC | 17 | 41244205 | 41244205 | + | Missense_Mutation | SNP | C | C | G | TCGA-34-2600-01A-01D-1522-08 | TCGA-34-2600-11A-01D-1522-08 | g.chr17:41244205C>G | c.3343G>C | c.(3343-3345)Gaa>Caa | p.E1115Q |
| LUSC | 17 | 41244844 | 41244844 | + | Missense_Mutation | SNP | C | C | G | TCGA-34-2600-01A-01D-1522-08 | TCGA-34-2600-11A-01D-1522-08 | g.chr17:41244844C>G | c.2704G>C | c.(2704-2706)Gaa>Caa | p.E902Q |
| LUSC | 17 | 41245215 | 41245215 | + | Missense_Mutation | SNP | C | C | T | TCGA-39-5037-01A-01D-1441-08 | TCGA-39-5037-11A-01D-1441-08 | g.chr17:41245215C>T | c.2333G>A | c.(2332-2334)gGc>gAc | p.G778D |
| LUSC | 17 | 41245974 | 41245974 | + | Missense_Mutation | SNP | A | A | G | TCGA-18-3409-01A-01D-0983-08 | TCGA-18-3409-11A-01D-0983-08 | g.chr17:41245974A>G | c.1574T>C | c.(1573-1575)gTt>gCt | p.V525A |
| LUSC | 17 | 41246004 | 41246004 | + | Missense_Mutation | SNP | T | T | A | TCGA-66-2756-01A-01D-1522-08 | TCGA-66-2756-11A-01D-1522-08 | g.chr17:41246004T>A | c.1544A>T | c.(1543-1545)gAg>gTg | p.E515V |
| LUSC | 17 | 41246321 | 41246321 | + | Silent | SNP | T | T | A | TCGA-18-5592-01A-01D-1632-08 | TCGA-18-5592-11A-11D-1632-08 | g.chr17:41246321T>A | c.1227A>T | c.(1225-1227)gtA>gtT | p.V409V |
| LUSC | 17 | 41246585 | 41246585 | + | Missense_Mutation | SNP | C | C | A | TCGA-39-5028-01A-01D-1441-08 | TCGA-39-5028-11A-01D-1441-08 | g.chr17:41246585C>A | c.963G>T | c.(961-963)tgG>tgT | p.W321C |
| LUSC | 17 | 41246589 | 41246589 | + | Missense_Mutation | SNP | C | C | G | TCGA-21-5782-01A-01D-1632-08 | TCGA-21-5782-10A-01D-1632-08 | g.chr17:41246589C>G | c.959G>C | c.(958-960)aGa>aCa | p.R320T |
| LUSC | 17 | 41256906 | 41256906 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-18-3421-01A-01D-0983-08 | TCGA-18-3421-11A-01D-0983-08 | g.chr17:41256906G>A | c.280C>T | c.(280-282)Cag>Tag | p.Q94* |
| OV | 17 | 41197784 | 41197784 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-13-0730-01A-01W-0370-10 | TCGA-13-0730-10B-01W-0370-10 | g.chr17:41197784G>A | c.5503C>T | c.(5503-5505)Cga>Tga | p.R1835* |
| OV | 17 | 41203135 | 41203135 | + | Splice_Site | SNP | C | C | A | TCGA-36-2534-01A-01D-1526-09 | TCGA-36-2534-10A-01D-1526-09 | g.chr17:41203135C>A | | c.e20-1 | |
| OV | 17 | 41215914 | 41215914 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-24-2035-01A-01W-0722-08 | TCGA-24-2035-10A-01W-0722-08 | g.chr17:41215914delC | c.5129delG | c.(5128-5130)ggafs | p.G1710fs |
| OV | 17 | 41226411 | 41226411 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-04-1357-01A-01W-0492-08 | TCGA-04-1357-11A-01W-0492-08 | g.chr17:41226411G>A | c.4612C>T | c.(4612-4614)Cag>Tag | p.Q1538* |
| OV | 17 | 41228504 | 41228504 | + | Splice_Site | DEL | C | C | - | TCGA-13-0761-01A-01W-0370-10 | TCGA-13-0761-10A-01W-0370-10 | g.chr17:41228504delC | | c.e13+1 | |
| OV | 17 | 41243753 | 41243754 | + | Frame_Shift_Ins | INS | - | - | TT | TCGA-13-1489-01A-01W-0549-09 | TCGA-13-1489-10A-01W-0549-09 | g.chr17:41243753_41243754insTT | c.3794_3795insAA | c.(3793-3795)aatfs | p.N1265fs |
| OV | 17 | 41243899 | 41243900 | + | Frame_Shift_Ins | INS | - | - | TAAGTTCT | TCGA-25-1632-01A-01W-0615-10 | TCGA-25-1632-10A-01W-0615-10 | g.chr17:41243899_41243900insTAAGTTCT | c.3648_3649insAGAACTTA | c.(3646-3651)ttatctfs | p.S1217fs |
| OV | 17 | 41243985 | 41243986 | + | Frame_Shift_Del | DEL | CT | CT | - | TCGA-29-1776-01A-01W-0639-09 | TCGA-29-1776-10A-01W-0639-09 | g.chr17:41243985_41243986delCT | c.3562_3563delAG | c.(3562-3564)aggfs | p.R1188fs |
| OV | 17 | 41244082 | 41244083 | + | Frame_Shift_Ins | INS | - | - | ATCTAACA | TCGA-24-1846-01A-01W-0639-09 | TCGA-24-1846-10A-01W-0639-09 | g.chr17:41244082_41244083insATCTAACA | c.3465_3466insTGTTAGAT | c.(3463-3468)gatgatfs | p.D1156fs |
| OV | 17 | 41245110 | 41245110 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-23-1026-01B-01W-0484-10 | TCGA-23-1026-10A-01W-0484-10 | g.chr17:41245110delC | c.2438delG | c.(2437-2439)ggafs | p.G813fs |
| OV | 17 | 41245150 | 41245150 | + | Nonsense_Mutation | SNP | T | T | A | TCGA-30-1857-01A-02W-0639-09 | TCGA-30-1857-10A-01W-0639-09 | g.chr17:41245150T>A | c.2398A>T | c.(2398-2400)Aaa>Taa | p.K800* |
| OV | 17 | 41245991 | 41245991 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-25-1630-01A-01W-0615-10 | TCGA-25-1630-10A-01W-0615-10 | g.chr17:41245991delC | c.1557delG | c.(1555-1557)aagfs | p.K520fs |
| OV | 17 | 41246127 | 41246127 | + | Nonsense_Mutation | SNP | A | A | C | TCGA-61-1914-01A-01W-0639-09 | TCGA-61-1914-11A-01W-0640-09 | g.chr17:41246127A>C | c.1421T>G | c.(1420-1422)tTa>tGa | p.L474* |
| OV | 17 | 41246256 | 41246256 | + | Nonsense_Mutation | SNP | A | A | C | TCGA-29-2427-01A-01W-0799-08 | TCGA-29-2427-10A-01W-0800-08 | g.chr17:41246256A>C | c.1292T>G | c.(1291-1293)tTa>tGa | p.L431* |
| OV | 17 | 41246666 | 41246666 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-29-1768-01A-01W-0633-09 | TCGA-29-1768-10A-01W-0634-09 | g.chr17:41246666delT | c.882delA | c.(880-882)aaafs | p.K294fs |
| OV | 17 | 41256234 | 41256234 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-25-1625-01A-01W-0615-10 | TCGA-25-1625-10A-01W-0615-10 | g.chr17:41256234C>A | c.346G>T | c.(346-348)Gaa>Taa | p.E116* |
| OV | 17 | 41256249 | 41256249 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-24-1847-01A-01W-0633-09 | TCGA-24-1847-10A-01W-0634-09 | g.chr17:41256249C>A | c.331G>T | c.(331-333)Gaa>Taa | p.E111* |
| OV | 17 | 41258544 | 41258544 | + | Missense_Mutation | SNP | G | G | C | TCGA-13-0804-01A-01W-0372-09 | TCGA-13-0804-10A-01W-0372-09 | g.chr17:41258544G>C | c.141C>G | c.(139-141)tgC>tgG | p.C47W |
| PAAD | 17 | 41223162 | 41223162 | + | Missense_Mutation | SNP | A | A | G | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr17:41223162A>G | c.4769T>C | c.(4768-4770)gTt>gCt | p.V1590A |
| PAAD | 17 | 41245612 | 41245612 | + | Missense_Mutation | SNP | T | T | C | TCGA-IB-AAUO-01A-12D-A38G-08 | TCGA-IB-AAUO-10A-01D-A38J-08 | g.chr17:41245612T>C | c.1936A>G | c.(1936-1938)Agc>Ggc | p.S646G |
| PAAD | 17 | 41246608 | 41246608 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr17:41246608C>T | c.940G>A | c.(940-942)Gca>Aca | p.A314T |
| PRAD | 17 | 41226394 | 41226394 | + | Silent | SNP | C | C | T | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr17:41226394C>T | c.4629G>A | c.(4627-4629)ggG>ggA | p.G1543G |
| PRAD | 17 | 41244008 | 41244008 | + | Silent | SNP | G | G | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr17:41244008G>A | c.3540C>T | c.(3538-3540)agC>agT | p.S1180S |
| PRAD | 17 | 41251796 | 41251796 | + | Missense_Mutation | SNP | T | T | G | TCGA-XQ-A8TA-01A-11D-A364-08 | TCGA-XQ-A8TA-10A-01D-A362-08 | g.chr17:41251796T>G | c.543A>C | c.(541-543)gaA>gaC | p.E181D |
| READ | 17 | 41197782 | 41197782 | + | Silent | SNP | T | T | C | TCGA-EI-6507-01A-11D-1733-10 | TCGA-EI-6507-10A-01D-1733-10 | g.chr17:41197782T>C | c.5505A>G | c.(5503-5505)cgA>cgG | p.R1835R |
| READ | 17 | 41197783 | 41197783 | + | Missense_Mutation | SNP | C | C | A | TCGA-EI-6506-01A-11D-1733-10 | TCGA-EI-6506-10A-01D-1733-10 | g.chr17:41197783C>A | c.5504G>T | c.(5503-5505)cGa>cTa | p.R1835L |
| READ | 17 | 41244523 | 41244523 | + | Missense_Mutation | SNP | A | A | G | TCGA-CI-6619-01B-11D-1826-10 | TCGA-CI-6619-10A-01D-1826-10 | g.chr17:41244523A>G | c.3025T>C | c.(3025-3027)Tca>Cca | p.S1009P |
| READ | 17 | 41246189 | 41246189 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr17:41246189C>A | c.1359G>T | c.(1357-1359)gaG>gaT | p.E453D |
| SKCM | 17 | 41209101 | 41209101 | + | Missense_Mutation | SNP | G | G | A | TCGA-ER-A3PL-06A-11D-A23B-08 | TCGA-ER-A3PL-10A-01D-A23B-08 | g.chr17:41209101G>A | c.5245C>T | c.(5245-5247)Cca>Tca | p.P1749S |
| SKCM | 17 | 41223166 | 41223166 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MS-06A-11D-A197-08 | TCGA-EE-A2MS-10A-01D-A199-08 | g.chr17:41223166G>A | c.4765C>T | c.(4765-4767)Cgt>Tgt | p.R1589C |
| SKCM | 17 | 41223222 | 41223222 | + | Missense_Mutation | SNP | A | A | G | TCGA-EE-A3JD-06A-11D-A20D-08 | TCGA-EE-A3JD-10A-01D-A20D-08 | g.chr17:41223222A>G | c.4709T>C | c.(4708-4710)cTc>cCc | p.L1570P |
| SKCM | 17 | 41223245 | 41223245 | + | Silent | SNP | A | A | G | TCGA-D3-A2JH-06A-11D-A196-08 | TCGA-D3-A2JH-10A-01D-A198-08 | g.chr17:41223245A>G | c.4686T>C | c.(4684-4686)ccT>ccC | p.P1562P |
| SKCM | 17 | 41243652 | 41243652 | + | Missense_Mutation | SNP | T | T | A | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr17:41243652T>A | c.3896A>T | c.(3895-3897)cAg>cTg | p.Q1299L |
| SKCM | 17 | 41243916 | 41243916 | + | Missense_Mutation | SNP | G | G | A | TCGA-GF-A6C9-06A-11D-A30X-08 | TCGA-GF-A6C9-10A-01D-A30X-08 | g.chr17:41243916G>A | c.3632C>T | c.(3631-3633)tCc>tTc | p.S1211F |
| SKCM | 17 | 41244176 | 41244176 | + | Silent | SNP | G | G | A | TCGA-D3-A3MV-06A-11D-A21A-08 | TCGA-D3-A3MV-10A-01D-A21A-08 | g.chr17:41244176G>A | c.3372C>T | c.(3370-3372)ttC>ttT | p.F1124F |
| SKCM | 17 | 41244256 | 41244256 | + | Missense_Mutation | SNP | G | G | T | TCGA-D3-A5GR-06A-11D-A27K-08 | TCGA-D3-A5GR-10A-01D-A27N-08 | g.chr17:41244256G>T | c.3292C>A | c.(3292-3294)Ctt>Att | p.L1098I |
| SKCM | 17 | 41244539 | 41244540 | + | Frame_Shift_Del | DEL | AA | AA | - | TCGA-ER-A19G-06A-11D-A196-08 | TCGA-ER-A19G-10A-01D-A198-08 | g.chr17:41244539_41244540delAA | c.3008_3009delTT | c.(3007-3009)tttfs | p.F1003fs |
| SKCM | 17 | 41244594 | 41244594 | + | Missense_Mutation | SNP | G | G | A | TCGA-FS-A1ZP-06A-11D-A197-08 | TCGA-FS-A1ZP-10A-01D-A199-08 | g.chr17:41244594G>A | c.2954C>T | c.(2953-2955)cCc>cTc | p.P985L |
| SKCM | 17 | 41244925 | 41244925 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr17:41244925G>A | c.2623C>T | c.(2623-2625)Cca>Tca | p.P875S |
| SKCM | 17 | 41245117 | 41245117 | + | Missense_Mutation | SNP | G | G | A | TCGA-ER-A42L-06A-11D-A24R-08 | TCGA-ER-A42L-10A-01D-A24R-08 | g.chr17:41245117G>A | c.2431C>T | c.(2431-2433)Ccc>Tcc | p.P811S |
| SKCM | 17 | 41246011 | 41246011 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr17:41246011G>A | c.1537C>T | c.(1537-1539)Cat>Tat | p.H513Y |
| SKCM | 17 | 41246107 | 41246107 | + | Silent | SNP | G | G | A | TCGA-EE-A3AG-06A-31D-A196-08 | TCGA-EE-A3AG-10A-01D-A198-08 | g.chr17:41246107G>A | c.1441C>T | c.(1441-1443)Cta>Tta | p.L481L |
| SKCM | 17 | 41246344 | 41246344 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MM-06A-11D-A196-08 | TCGA-EE-A2MM-10A-01D-A198-08 | g.chr17:41246344C>T | c.1204G>A | c.(1204-1206)Gag>Aag | p.E402K |
| SKCM | 17 | 41246734 | 41246734 | + | Missense_Mutation | SNP | C | C | T | TCGA-DA-A3F8-06A-11D-A20D-08 | TCGA-DA-A3F8-10A-01D-A20D-08 | g.chr17:41246734C>T | c.814G>A | c.(814-816)Gag>Aag | p.E272K |
| SKCM | 17 | 41246743 | 41246743 | + | Missense_Mutation | SNP | A | A | C | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr17:41246743A>C | c.805T>G | c.(805-807)Ttg>Gtg | p.L269V |
| SKCM | 17 | 41247929 | 41247929 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-EE-A20C-06A-11D-A196-08 | TCGA-EE-A20C-10A-01D-A198-08 | g.chr17:41247929G>A | c.604C>T | c.(604-606)Caa>Taa | p.Q202* |
| SKCM | 17 | 41256241 | 41256241 | + | Missense_Mutation | SNP | G | G | C | TCGA-GN-A4U3-06A-11D-A32N-08 | TCGA-GN-A4U3-10F-01D-A32N-08 | g.chr17:41256241G>C | c.339C>G | c.(337-339)aaC>aaG | p.N113K |