| Mutation - TCGA |
| Type | Chromosome | Start Position | End Position | Strand | Variant Classification | Variant Type | Reference Allele | Tumor_seq Allele 1 | Tumor_seq Allele 2 | Tumor Sample Barcode | Matched Norm Sample Barcode | Genome Change | cDNA Change | Codon Change | Protein Change |
|---|
| BLCA | 17 | 65822234 | 65822236 | + | In_Frame_Del | DEL | GAG | GAG | - | TCGA-XF-A8HI-01A-11D-A38G-08 | TCGA-XF-A8HI-10A-01D-A38J-08 | g.chr17:65822234_65822236delGAG | c.394_396delGAG | c.(394-396)gagdel | p.E138del |
| BLCA | 17 | 65850547 | 65850547 | + | Missense_Mutation | SNP | G | G | A | TCGA-KQ-A41Q-01A-11D-A339-08 | TCGA-KQ-A41Q-10D-01D-A339-08 | g.chr17:65850547G>A | c.1105G>A | c.(1105-1107)Gat>Aat | p.D369N |
| BLCA | 17 | 65850673 | 65850673 | + | Missense_Mutation | SNP | G | G | A | TCGA-XF-A9SX-01A-21D-A391-08 | TCGA-XF-A9SX-10A-01D-A394-08 | g.chr17:65850673G>A | c.1231G>A | c.(1231-1233)Gta>Ata | p.V411I |
| BLCA | 17 | 65850819 | 65850819 | + | Silent | SNP | A | A | G | TCGA-PQ-A6FN-01A-11D-A31L-08 | TCGA-PQ-A6FN-10A-01D-A31J-08 | g.chr17:65850819A>G | c.1377A>G | c.(1375-1377)gaA>gaG | p.E459E |
| BLCA | 17 | 65870932 | 65870932 | + | Splice_Site | SNP | G | G | T | TCGA-DK-A6AW-01A-11D-A30E-08 | TCGA-DK-A6AW-10A-01D-A30H-08 | g.chr17:65870932G>T | | c.e4-1 | |
| BLCA | 17 | 65871019 | 65871019 | + | Missense_Mutation | SNP | A | A | G | TCGA-FD-A3B7-01A-31D-A20D-08 | TCGA-FD-A3B7-10A-01D-A20D-08 | g.chr17:65871019A>G | c.1747A>G | c.(1747-1749)Act>Gct | p.T583A |
| BLCA | 17 | 65882295 | 65882295 | + | Missense_Mutation | SNP | C | C | T | TCGA-DK-A1AB-01A-11D-A13W-08 | TCGA-DK-A1AB-10A-01D-A13W-08 | g.chr17:65882295C>T | c.2105C>T | c.(2104-2106)tCc>tTc | p.S702F |
| BLCA | 17 | 65882426 | 65882426 | + | Missense_Mutation | SNP | G | G | C | TCGA-CF-A27C-01A-11D-A16O-08 | TCGA-CF-A27C-10A-01D-A16O-08 | g.chr17:65882426G>C | c.2236G>C | c.(2236-2238)Gag>Cag | p.E746Q |
| BLCA | 17 | 65888045 | 65888045 | + | Silent | SNP | C | C | T | TCGA-E7-A85H-01A-11D-A34U-08 | TCGA-E7-A85H-10B-01D-A34X-08 | g.chr17:65888045C>T | c.2328C>T | c.(2326-2328)atC>atT | p.I776I |
| BLCA | 17 | 65888148 | 65888148 | + | Missense_Mutation | SNP | G | G | C | TCGA-DK-AA6L-01A-11D-A391-08 | TCGA-DK-AA6L-10A-01D-A394-08 | g.chr17:65888148G>C | c.2431G>C | c.(2431-2433)Gag>Cag | p.E811Q |
| BLCA | 17 | 65889808 | 65889808 | + | Missense_Mutation | SNP | C | C | T | TCGA-DK-A1AF-01A-11D-A13W-08 | TCGA-DK-A1AF-10A-01D-A13W-08 | g.chr17:65889808C>T | c.2756C>T | c.(2755-2757)tCa>tTa | p.S919L |
| BLCA | 17 | 65890162 | 65890162 | + | Missense_Mutation | SNP | C | C | G | TCGA-BT-A3PJ-01A-21D-A21Z-08 | TCGA-BT-A3PJ-10A-01D-A21Z-08 | g.chr17:65890162C>G | c.2802C>G | c.(2800-2802)atC>atG | p.I934M |
| BLCA | 17 | 65905851 | 65905851 | + | Missense_Mutation | SNP | C | C | T | TCGA-KQ-A41P-01A-12D-A339-08 | TCGA-KQ-A41P-10F-01D-A339-08 | g.chr17:65905851C>T | c.3344C>T | c.(3343-3345)tCa>tTa | p.S1115L |
| BLCA | 17 | 65907091 | 65907091 | + | Missense_Mutation | SNP | C | C | A | TCGA-DK-A3IQ-01A-31D-A20D-08 | TCGA-DK-A3IQ-10A-01D-A20D-08 | g.chr17:65907091C>A | c.3469C>A | c.(3469-3471)Cag>Aag | p.Q1157K |
| BLCA | 17 | 65907246 | 65907246 | + | Missense_Mutation | SNP | C | C | G | TCGA-G2-AA3C-01A-21D-A391-08 | TCGA-G2-AA3C-10A-01D-A394-08 | g.chr17:65907246C>G | c.3624C>G | c.(3622-3624)atC>atG | p.I1208M |
| BLCA | 17 | 65907303 | 65907304 | + | Frame_Shift_Del | DEL | TC | TC | - | TCGA-S5-AA26-01A-11D-A38G-08 | TCGA-S5-AA26-10A-01D-A38J-08 | g.chr17:65907303_65907304delTC | c.3681_3682delTC | c.(3679-3684)aatctcfs | p.L1228fs |
| BLCA | 17 | 65907308 | 65907308 | + | Missense_Mutation | SNP | C | C | G | TCGA-4Z-AA84-01A-11D-A391-08 | TCGA-4Z-AA84-10A-01D-A394-08 | g.chr17:65907308C>G | c.3686C>G | c.(3685-3687)tCt>tGt | p.S1229C |
| BLCA | 17 | 65907442 | 65907442 | + | Missense_Mutation | SNP | C | C | T | TCGA-4Z-AA86-01A-11D-A391-08 | TCGA-4Z-AA86-10A-01D-A394-08 | g.chr17:65907442C>T | c.3820C>T | c.(3820-3822)Ctt>Ttt | p.L1274F |
| BLCA | 17 | 65907510 | 65907510 | + | Silent | SNP | C | C | T | TCGA-DK-A6AW-01A-11D-A30E-08 | TCGA-DK-A6AW-10A-01D-A30H-08 | g.chr17:65907510C>T | c.3888C>T | c.(3886-3888)gtC>gtT | p.V1296V |
| BLCA | 17 | 65907526 | 65907526 | + | Missense_Mutation | SNP | G | G | A | TCGA-C4-A0EZ-01A-21D-A10S-08 | TCGA-C4-A0EZ-10A-01D-A10S-08 | g.chr17:65907526G>A | c.3904G>A | c.(3904-3906)Gaa>Aaa | p.E1302K |
| BLCA | 17 | 65907711 | 65907711 | + | Silent | SNP | C | C | T | TCGA-G2-AA3C-01A-21D-A391-08 | TCGA-G2-AA3C-10A-01D-A394-08 | g.chr17:65907711C>T | c.4089C>T | c.(4087-4089)ctC>ctT | p.L1363L |
| BLCA | 17 | 65907743 | 65907743 | + | Missense_Mutation | SNP | C | C | T | TCGA-GV-A6ZA-01A-12D-A339-08 | TCGA-GV-A6ZA-10A-01D-A339-08 | g.chr17:65907743C>T | c.4121C>T | c.(4120-4122)tCt>tTt | p.S1374F |
| BLCA | 17 | 65907937 | 65907937 | + | Missense_Mutation | SNP | G | G | C | TCGA-FD-A6TC-01A-21D-A339-08 | TCGA-FD-A6TC-10A-21D-A339-08 | g.chr17:65907937G>C | c.4315G>C | c.(4315-4317)Gaa>Caa | p.E1439Q |
| BLCA | 17 | 65908180 | 65908180 | + | Missense_Mutation | SNP | G | G | C | TCGA-FJ-A3Z7-01A-12D-A23M-08 | TCGA-FJ-A3Z7-10A-01D-A23K-08 | g.chr17:65908180G>C | c.4558G>C | c.(4558-4560)Gag>Cag | p.E1520Q |
| BLCA | 17 | 65908454 | 65908454 | + | Missense_Mutation | SNP | C | C | T | TCGA-DK-A6AW-01A-11D-A30E-08 | TCGA-DK-A6AW-10A-01D-A30H-08 | g.chr17:65908454C>T | c.4832C>T | c.(4831-4833)tCg>tTg | p.S1611L |
| BLCA | 17 | 65908474 | 65908474 | + | Missense_Mutation | SNP | G | G | A | TCGA-FD-A3SN-01A-12D-A22Z-08 | TCGA-FD-A3SN-10A-01D-A22Z-08 | g.chr17:65908474G>A | c.4852G>A | c.(4852-4854)Gat>Aat | p.D1618N |
| BLCA | 17 | 65908616 | 65908616 | + | Missense_Mutation | SNP | C | C | T | TCGA-G2-AA3C-01A-21D-A391-08 | TCGA-G2-AA3C-10A-01D-A394-08 | g.chr17:65908616C>T | c.4994C>T | c.(4993-4995)tCa>tTa | p.S1665L |
| BLCA | 17 | 65908875 | 65908875 | + | Silent | SNP | C | C | T | TCGA-DK-AA75-01A-11D-A391-08 | TCGA-DK-AA75-10A-01D-A394-08 | g.chr17:65908875C>T | c.5253C>T | c.(5251-5253)gtC>gtT | p.V1751V |
| BLCA | 17 | 65909041 | 65909041 | + | Missense_Mutation | SNP | G | G | C | TCGA-UY-A9PD-01A-11D-A38G-08 | TCGA-UY-A9PD-10A-01D-A38J-08 | g.chr17:65909041G>C | c.5419G>C | c.(5419-5421)Gag>Cag | p.E1807Q |
| BLCA | 17 | 65914842 | 65914842 | + | Silent | SNP | G | G | A | TCGA-ZF-AA51-01A-21D-A391-08 | TCGA-ZF-AA51-10A-01D-A394-08 | g.chr17:65914842G>A | c.5694G>A | c.(5692-5694)caG>caA | p.Q1898Q |
| BLCA | 17 | 65919001 | 65919001 | + | Missense_Mutation | SNP | G | G | A | TCGA-XF-A9T3-01A-11D-A42E-08 | TCGA-XF-A9T3-10A-01D-A42H-08 | g.chr17:65919001G>A | c.5981G>A | c.(5980-5982)cGg>cAg | p.R1994Q |
| BLCA | 17 | 65925584 | 65925584 | + | Missense_Mutation | SNP | G | G | A | TCGA-DK-A2I4-01A-11D-A21A-08 | TCGA-DK-A2I4-10A-01D-A21A-08 | g.chr17:65925584G>A | c.6509G>A | c.(6508-6510)gGa>gAa | p.G2170E |
| BLCA | 17 | 65941562 | 65941562 | + | Silent | SNP | G | G | A | TCGA-GV-A3JW-01A-11D-A20D-08 | TCGA-GV-A3JW-10A-01D-A20D-08 | g.chr17:65941562G>A | c.7116G>A | c.(7114-7116)caG>caA | p.Q2372Q |
| BLCA | 17 | 65942064 | 65942064 | + | Missense_Mutation | SNP | A | A | T | TCGA-E7-A5KE-01A-11D-A289-08 | TCGA-E7-A5KE-10A-01D-A289-08 | g.chr17:65942064A>T | c.7618A>T | c.(7618-7620)Act>Tct | p.T2540S |
| BLCA | 17 | 65942143 | 65942143 | + | Missense_Mutation | SNP | A | A | T | TCGA-UY-A78K-01A-11D-A339-08 | TCGA-UY-A78K-10A-01D-A339-08 | g.chr17:65942143A>T | c.7697A>T | c.(7696-7698)cAa>cTa | p.Q2566L |
| BLCA | 17 | 65942274 | 65942274 | + | Missense_Mutation | SNP | C | C | T | TCGA-GC-A3RB-01A-12D-A21Z-08 | TCGA-GC-A3RB-10A-01D-A21Z-08 | g.chr17:65942274C>T | c.7828C>T | c.(7828-7830)Cac>Tac | p.H2610Y |
| BLCA | 17 | 65942319 | 65942319 | + | Missense_Mutation | SNP | G | G | A | TCGA-FD-A5BZ-01A-11D-A289-08 | TCGA-FD-A5BZ-10A-01D-A289-08 | g.chr17:65942319G>A | c.7873G>A | c.(7873-7875)Gag>Aag | p.E2625K |
| BLCA | 17 | 65942424 | 65942424 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-BL-A5ZZ-01A-31D-A30E-08 | TCGA-BL-A5ZZ-10A-01D-A30H-08 | g.chr17:65942424G>T | c.7978G>T | c.(7978-7980)Gaa>Taa | p.E2660* |
| BLCA | 17 | 65944344 | 65944344 | + | Silent | SNP | C | C | T | TCGA-UY-A9PH-01A-11D-A38G-08 | TCGA-UY-A9PH-10A-01D-A38J-08 | g.chr17:65944344C>T | c.8226C>T | c.(8224-8226)ttC>ttT | p.F2742F |
| BLCA | 17 | 65978372 | 65978372 | + | Missense_Mutation | SNP | C | C | G | TCGA-DK-AA76-01A-11D-A391-08 | TCGA-DK-AA76-10A-01D-A394-08 | g.chr17:65978372C>G | c.9109C>G | c.(9109-9111)Cat>Gat | p.H3037D |
| BRCA | 17 | 65850193 | 65850193 | + | Missense_Mutation | SNP | G | G | A | TCGA-D8-A27G-01A-11D-A16D-09 | TCGA-D8-A27G-10A-01D-A16D-09 | g.chr17:65850193G>A | c.751G>A | c.(751-753)Gag>Aag | p.E251K |
| BRCA | 17 | 65850252 | 65850252 | + | Silent | SNP | T | T | C | TCGA-A1-A0SN-01A-11D-A142-09 | TCGA-A1-A0SN-10B-01D-A142-09 | g.chr17:65850252T>C | c.810T>C | c.(808-810)ttT>ttC | p.F270F |
| BRCA | 17 | 65871671 | 65871671 | + | Splice_Site | SNP | G | G | C | TCGA-AO-A03M-01B-11D-A10M-09 | TCGA-AO-A03M-10A-01D-A10M-09 | g.chr17:65871671G>C | | c.e5-1 | |
| BRCA | 17 | 65905793 | 65905793 | + | Missense_Mutation | SNP | G | G | C | TCGA-C8-A26Y-01A-11D-A16D-09 | TCGA-C8-A26Y-10A-01D-A16D-09 | g.chr17:65905793G>C | c.3286G>C | c.(3286-3288)Gat>Cat | p.D1096H |
| BRCA | 17 | 65908221 | 65908221 | + | Missense_Mutation | SNP | A | A | G | TCGA-A7-A4SE-01A-11D-A25Q-09 | TCGA-A7-A4SE-10A-01D-A25Q-09 | g.chr17:65908221A>G | c.4599A>G | c.(4597-4599)atA>atG | p.I1533M |
| BRCA | 17 | 65908442 | 65908442 | + | Missense_Mutation | SNP | C | C | G | TCGA-D8-A1JA-01A-11D-A13L-09 | TCGA-D8-A1JA-10A-01W-A14R-09 | g.chr17:65908442C>G | c.4820C>G | c.(4819-4821)tCc>tGc | p.S1607C |
| BRCA | 17 | 65908824 | 65908824 | + | Silent | SNP | C | C | A | TCGA-AO-A128-01A-11D-A10M-09 | TCGA-AO-A128-10A-01D-A10M-09 | g.chr17:65908824C>A | c.5202C>A | c.(5200-5202)ggC>ggA | p.G1734G |
| BRCA | 17 | 65908868 | 65908868 | + | Missense_Mutation | SNP | C | C | G | TCGA-AO-A03M-01B-11D-A10M-09 | TCGA-AO-A03M-10A-01D-A10M-09 | g.chr17:65908868C>G | c.5246C>G | c.(5245-5247)tCc>tGc | p.S1749C |
| BRCA | 17 | 65909295 | 65909295 | + | Silent | SNP | C | C | A | TCGA-BH-A18J-01A-11D-A12B-09 | TCGA-BH-A18J-11A-31D-A12B-09 | g.chr17:65909295C>A | c.5673C>A | c.(5671-5673)atC>atA | p.I1891I |
| BRCA | 17 | 65914927 | 65914927 | + | Missense_Mutation | SNP | C | C | A | TCGA-C8-A132-01A-31D-A10Y-09 | TCGA-C8-A132-10A-01D-A110-09 | g.chr17:65914927C>A | c.5779C>A | c.(5779-5781)Cct>Act | p.P1927T |
| BRCA | 17 | 65914930 | 65914930 | + | Missense_Mutation | SNP | C | C | T | TCGA-OL-A5RU-01A-11D-A28B-09 | TCGA-OL-A5RU-10A-01D-A28E-09 | g.chr17:65914930C>T | c.5782C>T | c.(5782-5784)Cca>Tca | p.P1928S |
| BRCA | 17 | 65916216 | 65916216 | + | Missense_Mutation | SNP | C | C | G | TCGA-BH-A0DZ-01A-11W-A019-09 | TCGA-BH-A0DZ-10A-01W-A021-09 | g.chr17:65916216C>G | c.5892C>G | c.(5890-5892)atC>atG | p.I1964M |
| BRCA | 17 | 65925453 | 65925453 | + | Splice_Site | SNP | C | C | T | TCGA-A8-A082-01A-11W-A019-09 | TCGA-A8-A082-10A-01W-A021-09 | g.chr17:65925453C>T | c.6378C>T | c.(6376-6378)ggC>ggT | p.G2126G |
| BRCA | 17 | 65925540 | 65925540 | + | Missense_Mutation | SNP | G | G | T | TCGA-EW-A1PD-01A-11D-A142-09 | TCGA-EW-A1PD-10A-01D-A142-09 | g.chr17:65925540G>T | c.6465G>T | c.(6463-6465)agG>agT | p.R2155S |
| BRCA | 17 | 65928070 | 65928070 | + | Missense_Mutation | SNP | G | G | C | TCGA-AC-A23H-01A-11D-A159-09 | TCGA-AC-A23H-11A-12D-A17G-09 | g.chr17:65928070G>C | c.6572G>C | c.(6571-6573)aGa>aCa | p.R2191T |
| BRCA | 17 | 65936663 | 65936663 | + | Missense_Mutation | SNP | C | C | T | TCGA-BH-A2L8-01A-11D-A18P-09 | TCGA-BH-A2L8-10A-01D-A18P-09 | g.chr17:65936663C>T | c.6746C>T | c.(6745-6747)tCa>tTa | p.S2249L |
| BRCA | 17 | 65955782 | 65955783 | + | In_Frame_Ins | INS | - | - | GCC | TCGA-A7-A0CE-01A-11W-A019-09 | TCGA-A7-A0CE-10A-01W-A021-09 | g.chr17:65955782_65955783insGCC | c.8430_8431insGCC | c.(8431-8433)cct>GCCcct | p.2810_2811insA |
| CESC | 17 | 65822382 | 65822382 | + | Missense_Mutation | SNP | A | A | G | TCGA-FU-A3NI-01A-11D-A21Q-09 | TCGA-FU-A3NI-10A-01D-A21Q-09 | g.chr17:65822382A>G | c.542A>G | c.(541-543)gAc>gGc | p.D181G |
| CESC | 17 | 65850325 | 65850325 | + | Missense_Mutation | SNP | C | C | G | TCGA-JW-A5VL-01A-11D-A28B-09 | TCGA-JW-A5VL-10A-01D-A28E-09 | g.chr17:65850325C>G | c.883C>G | c.(883-885)Ctg>Gtg | p.L295V |
| CESC | 17 | 65888007 | 65888007 | + | Missense_Mutation | SNP | C | C | G | TCGA-UC-A7PD-01A-11D-A351-09 | TCGA-UC-A7PD-11A-12D-A351-09 | g.chr17:65888007C>G | c.2290C>G | c.(2290-2292)Cct>Gct | p.P764A |
| CESC | 17 | 65888035 | 65888035 | + | Nonsense_Mutation | SNP | C | C | G | TCGA-C5-A1BQ-01C-11D-A20U-09 | TCGA-C5-A1BQ-10A-01D-A20U-09 | g.chr17:65888035C>G | c.2318C>G | c.(2317-2319)tCa>tGa | p.S773* |
| CESC | 17 | 65889808 | 65889808 | + | Missense_Mutation | SNP | C | C | T | TCGA-LP-A4AV-01A-11D-A243-09 | TCGA-LP-A4AV-10A-01D-A243-09 | g.chr17:65889808C>T | c.2756C>T | c.(2755-2757)tCa>tTa | p.S919L |
| CESC | 17 | 65907170 | 65907170 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-FU-A2QG-01A-11D-A18J-09 | TCGA-FU-A2QG-10A-01D-A18J-09 | g.chr17:65907170C>A | c.3548C>A | c.(3547-3549)tCa>tAa | p.S1183* |
| CESC | 17 | 65907505 | 65907505 | + | Missense_Mutation | SNP | G | G | A | TCGA-C5-A1BQ-01C-11D-A20U-09 | TCGA-C5-A1BQ-10A-01D-A20U-09 | g.chr17:65907505G>A | c.3883G>A | c.(3883-3885)Gat>Aat | p.D1295N |
| CESC | 17 | 65907913 | 65907913 | + | Missense_Mutation | SNP | G | G | T | TCGA-FU-A3HZ-01A-11D-A20U-09 | TCGA-FU-A3HZ-10A-01D-A20U-09 | g.chr17:65907913G>T | c.4291G>T | c.(4291-4293)Gat>Tat | p.D1431Y |
| CESC | 17 | 65908690 | 65908690 | + | Missense_Mutation | SNP | G | G | A | TCGA-Q1-A73O-01A-11D-A32I-09 | TCGA-Q1-A73O-10B-01D-A32I-09 | g.chr17:65908690G>A | c.5068G>A | c.(5068-5070)Gaa>Aaa | p.E1690K |
| CESC | 17 | 65908943 | 65908943 | + | Missense_Mutation | SNP | C | C | G | TCGA-Q1-A6DW-01A-11D-A32I-09 | TCGA-Q1-A6DW-10B-01D-A32I-09 | g.chr17:65908943C>G | c.5321C>G | c.(5320-5322)tCt>tGt | p.S1774C |
| CESC | 17 | 65914901 | 65914901 | + | Missense_Mutation | SNP | G | G | A | TCGA-C5-A1M8-01A-21D-A13W-08 | TCGA-C5-A1M8-10A-01D-A13W-08 | g.chr17:65914901G>A | c.5753G>A | c.(5752-5754)aGa>aAa | p.R1918K |
| CESC | 17 | 65941593 | 65941593 | + | Missense_Mutation | SNP | C | C | T | TCGA-FU-A23L-01A-11D-A16O-08 | TCGA-FU-A23L-10A-01D-A16O-08 | g.chr17:65941593C>T | c.7147C>T | c.(7147-7149)Cca>Tca | p.P2383S |
| COAD | 17 | 65822426 | 65822426 | + | Missense_Mutation | SNP | A | A | G | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr17:65822426A>G | c.586A>G | c.(586-588)Agc>Ggc | p.S196G |
| COAD | 17 | 65850818 | 65850818 | + | Missense_Mutation | SNP | A | A | G | TCGA-A6-6780-01A-11D-1835-10 | TCGA-A6-6780-10A-01D-1835-10 | g.chr17:65850818A>G | c.1376A>G | c.(1375-1377)gAa>gGa | p.E459G |
| COAD | 17 | 65882420 | 65882420 | + | Missense_Mutation | SNP | C | C | G | TCGA-AA-3815-01A-01W-0995-10 | TCGA-AA-3815-10A-01W-0995-10 | g.chr17:65882420C>G | c.2230C>G | c.(2230-2232)Cag>Gag | p.Q744E |
| COAD | 17 | 65890193 | 65890193 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr17:65890193G>T | c.2833G>T | c.(2833-2835)Gaa>Taa | p.E945* |
| COAD | 17 | 65890283 | 65890283 | + | Splice_Site | SNP | T | T | C | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr17:65890283T>C | | c.e9+2 | |
| COAD | 17 | 65900840 | 65900840 | + | Missense_Mutation | SNP | A | A | C | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr17:65900840A>C | c.3074A>C | c.(3073-3075)gAg>gCg | p.E1025A |
| COAD | 17 | 65900888 | 65900888 | + | Missense_Mutation | SNP | A | A | T | TCGA-AA-3819-01A-01W-0900-09 | TCGA-AA-3819-10A-01W-0900-09 | g.chr17:65900888A>T | c.3122A>T | c.(3121-3123)cAt>cTt | p.H1041L |
| COAD | 17 | 65900903 | 65900903 | + | Missense_Mutation | SNP | T | T | C | TCGA-AD-6889-01A-11D-1924-10 | TCGA-AD-6889-10A-01D-1924-10 | g.chr17:65900903T>C | c.3137T>C | c.(3136-3138)gTt>gCt | p.V1046A |
| COAD | 17 | 65905854 | 65905854 | + | Missense_Mutation | SNP | A | A | C | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr17:65905854A>C | c.3347A>C | c.(3346-3348)aAg>aCg | p.K1116T |
| COAD | 17 | 65907159 | 65907159 | + | Missense_Mutation | SNP | G | G | T | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chr17:65907159G>T | c.3537G>T | c.(3535-3537)aaG>aaT | p.K1179N |
| COAD | 17 | 65907603 | 65907603 | + | Missense_Mutation | SNP | G | G | C | TCGA-F4-6703-01A-11D-1835-10 | TCGA-F4-6703-10A-01D-1835-10 | g.chr17:65907603G>C | c.3981G>C | c.(3979-3981)caG>caC | p.Q1327H |
| COAD | 17 | 65907729 | 65907729 | + | Silent | SNP | C | C | T | TCGA-G4-6586-01A-11D-1771-10 | TCGA-G4-6586-10A-01D-1771-10 | g.chr17:65907729C>T | c.4107C>T | c.(4105-4107)gaC>gaT | p.D1369D |
| COAD | 17 | 65907749 | 65907749 | + | Missense_Mutation | SNP | A | A | G | TCGA-AY-6197-01A-11D-1719-10 | TCGA-AY-6197-10A-01D-1719-10 | g.chr17:65907749A>G | c.4127A>G | c.(4126-4128)aAg>aGg | p.K1376R |
| COAD | 17 | 65907749 | 65907749 | + | Missense_Mutation | SNP | A | A | G | TCGA-CM-5349-01A-21D-1719-10 | TCGA-CM-5349-10A-01D-1719-10 | g.chr17:65907749A>G | c.4127A>G | c.(4126-4128)aAg>aGg | p.K1376R |
| COAD | 17 | 65908188 | 65908188 | + | Missense_Mutation | SNP | A | A | T | TCGA-D5-5540-01A-01D-1650-10 | TCGA-D5-5540-10A-01D-1650-10 | g.chr17:65908188A>T | c.4566A>T | c.(4564-4566)gaA>gaT | p.E1522D |
| COAD | 17 | 65908497 | 65908497 | + | Silent | SNP | T | T | C | TCGA-AA-3864-01A-01W-0995-10 | TCGA-AA-3864-10A-01W-0995-10 | g.chr17:65908497T>C | c.4875T>C | c.(4873-4875)gaT>gaC | p.D1625D |
| COAD | 17 | 65908824 | 65908824 | + | Silent | SNP | C | C | T | TCGA-A6-2676-01A-01W-0833-10 | TCGA-A6-2676-10A-01W-0833-10 | g.chr17:65908824C>T | c.5202C>T | c.(5200-5202)ggC>ggT | p.G1734G |
| COAD | 17 | 65916200 | 65916200 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr17:65916200G>A | c.5876G>A | c.(5875-5877)cGa>cAa | p.R1959Q |
| COAD | 17 | 65924641 | 65924641 | + | Silent | SNP | T | T | C | TCGA-AA-3516-01A-02W-0833-10 | TCGA-AA-3516-10A-01W-0833-10 | g.chr17:65924641T>C | c.6300T>C | c.(6298-6300)gcT>gcC | p.A2100A |
| COAD | 17 | 65928032 | 65928032 | + | Silent | SNP | C | C | T | TCGA-F4-6856-01A-11D-1924-10 | TCGA-F4-6856-10A-01D-1924-10 | g.chr17:65928032C>T | c.6534C>T | c.(6532-6534)atC>atT | p.I2178I |
| COAD | 17 | 65941553 | 65941553 | + | Silent | SNP | G | G | A | TCGA-AA-A00J-01A-02W-A005-10 | TCGA-AA-A00J-10A-01W-A005-10 | g.chr17:65941553G>A | c.7107G>A | c.(7105-7107)ctG>ctA | p.L2369L |
| COAD | 17 | 65941738 | 65941738 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3864-01A-01W-0995-10 | TCGA-AA-3864-10A-01W-0995-10 | g.chr17:65941738T>C | c.7292T>C | c.(7291-7293)gTt>gCt | p.V2431A |
| COAD | 17 | 65941878 | 65941878 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3555-01A-01W-0831-10 | TCGA-AA-3555-10A-01W-0831-10 | g.chr17:65941878C>T | c.7432C>T | c.(7432-7434)Cgt>Tgt | p.R2478C |
| COAD | 17 | 65942315 | 65942315 | + | Silent | SNP | G | G | A | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr17:65942315G>A | c.7869G>A | c.(7867-7869)gtG>gtA | p.V2623V |
| COAD | 17 | 65942392 | 65942392 | + | Missense_Mutation | SNP | G | G | A | TCGA-D5-6928-01A-11D-1924-10 | TCGA-D5-6928-10A-01D-1924-10 | g.chr17:65942392G>A | c.7946G>A | c.(7945-7947)cGt>cAt | p.R2649H |
| COAD | 17 | 65943891 | 65943891 | + | Missense_Mutation | SNP | G | G | A | TCGA-CA-5254-01A-21D-1835-10 | TCGA-CA-5254-10A-01D-1835-10 | g.chr17:65943891G>A | c.8045G>A | c.(8044-8046)aGc>aAc | p.S2682N |
| COAD | 17 | 65944279 | 65944279 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr17:65944279C>T | c.8161C>T | c.(8161-8163)Cgt>Tgt | p.R2721C |
| COAD | 17 | 65955870 | 65955870 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3848-01A-01W-0900-09 | TCGA-AA-3848-10A-01W-0900-09 | g.chr17:65955870G>A | c.8518G>A | c.(8518-8520)Gaa>Aaa | p.E2840K |
| COAD | 17 | 65971931 | 65971931 | + | Silent | SNP | A | A | G | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr17:65971931A>G | c.8961A>G | c.(8959-8961)gaA>gaG | p.E2987E |
| COADREAD | 17 | 65822426 | 65822426 | + | Missense_Mutation | SNP | A | A | G | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr17:65822426A>G | c.586A>G | c.(586-588)Agc>Ggc | p.S196G |
| COADREAD | 17 | 65850818 | 65850818 | + | Missense_Mutation | SNP | A | A | G | TCGA-A6-6780-01A-11D-1835-10 | TCGA-A6-6780-10A-01D-1835-10 | g.chr17:65850818A>G | c.1376A>G | c.(1375-1377)gAa>gGa | p.E459G |
| COADREAD | 17 | 65871774 | 65871774 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr17:65871774G>A | c.1967G>A | c.(1966-1968)aGc>aAc | p.S656N |
| COADREAD | 17 | 65882420 | 65882420 | + | Missense_Mutation | SNP | C | C | G | TCGA-AA-3815-01A-01W-0995-10 | TCGA-AA-3815-10A-01W-0995-10 | g.chr17:65882420C>G | c.2230C>G | c.(2230-2232)Cag>Gag | p.Q744E |
| COADREAD | 17 | 65890193 | 65890193 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr17:65890193G>T | c.2833G>T | c.(2833-2835)Gaa>Taa | p.E945* |
| COADREAD | 17 | 65890193 | 65890193 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr17:65890193G>T | c.2833G>T | c.(2833-2835)Gaa>Taa | p.E945* |
| COADREAD | 17 | 65890283 | 65890283 | + | Splice_Site | SNP | T | T | C | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr17:65890283T>C | | c.e9+2 | |
| COADREAD | 17 | 65900840 | 65900840 | + | Missense_Mutation | SNP | A | A | C | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chr17:65900840A>C | c.3074A>C | c.(3073-3075)gAg>gCg | p.E1025A |
| COADREAD | 17 | 65900869 | 65900869 | + | Missense_Mutation | SNP | A | A | G | TCGA-DC-6160-01A-11D-1657-10 | TCGA-DC-6160-10A-01D-1657-10 | g.chr17:65900869A>G | c.3103A>G | c.(3103-3105)Agc>Ggc | p.S1035G |
| COADREAD | 17 | 65900888 | 65900888 | + | Missense_Mutation | SNP | A | A | T | TCGA-AA-3819-01A-01W-0900-09 | TCGA-AA-3819-10A-01W-0900-09 | g.chr17:65900888A>T | c.3122A>T | c.(3121-3123)cAt>cTt | p.H1041L |
| COADREAD | 17 | 65900903 | 65900903 | + | Missense_Mutation | SNP | T | T | C | TCGA-AD-6889-01A-11D-1924-10 | TCGA-AD-6889-10A-01D-1924-10 | g.chr17:65900903T>C | c.3137T>C | c.(3136-3138)gTt>gCt | p.V1046A |
| COADREAD | 17 | 65905854 | 65905854 | + | Missense_Mutation | SNP | A | A | C | TCGA-CA-6717-01A-11D-1835-10 | TCGA-CA-6717-10A-01D-1835-10 | g.chr17:65905854A>C | c.3347A>C | c.(3346-3348)aAg>aCg | p.K1116T |
| COADREAD | 17 | 65907077 | 65907077 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr17:65907077C>A | c.3455C>A | c.(3454-3456)tCa>tAa | p.S1152* |
| COADREAD | 17 | 65907159 | 65907159 | + | Missense_Mutation | SNP | G | G | T | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chr17:65907159G>T | c.3537G>T | c.(3535-3537)aaG>aaT | p.K1179N |
| COADREAD | 17 | 65907603 | 65907603 | + | Missense_Mutation | SNP | G | G | C | TCGA-F4-6703-01A-11D-1835-10 | TCGA-F4-6703-10A-01D-1835-10 | g.chr17:65907603G>C | c.3981G>C | c.(3979-3981)caG>caC | p.Q1327H |
| COADREAD | 17 | 65907729 | 65907729 | + | Silent | SNP | C | C | T | TCGA-G4-6586-01A-11D-1771-10 | TCGA-G4-6586-10A-01D-1771-10 | g.chr17:65907729C>T | c.4107C>T | c.(4105-4107)gaC>gaT | p.D1369D |
| COADREAD | 17 | 65907749 | 65907749 | + | Missense_Mutation | SNP | A | A | G | TCGA-AY-6197-01A-11D-1719-10 | TCGA-AY-6197-10A-01D-1719-10 | g.chr17:65907749A>G | c.4127A>G | c.(4126-4128)aAg>aGg | p.K1376R |
| COADREAD | 17 | 65907749 | 65907749 | + | Missense_Mutation | SNP | A | A | G | TCGA-CM-5349-01A-21D-1719-10 | TCGA-CM-5349-10A-01D-1719-10 | g.chr17:65907749A>G | c.4127A>G | c.(4126-4128)aAg>aGg | p.K1376R |
| COADREAD | 17 | 65908188 | 65908188 | + | Missense_Mutation | SNP | A | A | T | TCGA-D5-5540-01A-01D-1650-10 | TCGA-D5-5540-10A-01D-1650-10 | g.chr17:65908188A>T | c.4566A>T | c.(4564-4566)gaA>gaT | p.E1522D |
| COADREAD | 17 | 65908497 | 65908497 | + | Silent | SNP | T | T | C | TCGA-AA-3864-01A-01W-0995-10 | TCGA-AA-3864-10A-01W-0995-10 | g.chr17:65908497T>C | c.4875T>C | c.(4873-4875)gaT>gaC | p.D1625D |
| COADREAD | 17 | 65908824 | 65908824 | + | Silent | SNP | C | C | T | TCGA-A6-2676-01A-01W-0833-10 | TCGA-A6-2676-10A-01W-0833-10 | g.chr17:65908824C>T | c.5202C>T | c.(5200-5202)ggC>ggT | p.G1734G |
| COADREAD | 17 | 65916200 | 65916200 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chr17:65916200G>A | c.5876G>A | c.(5875-5877)cGa>cAa | p.R1959Q |
| COADREAD | 17 | 65924641 | 65924641 | + | Silent | SNP | T | T | C | TCGA-AA-3516-01A-02W-0833-10 | TCGA-AA-3516-10A-01W-0833-10 | g.chr17:65924641T>C | c.6300T>C | c.(6298-6300)gcT>gcC | p.A2100A |
| COADREAD | 17 | 65928032 | 65928032 | + | Silent | SNP | C | C | T | TCGA-F4-6856-01A-11D-1924-10 | TCGA-F4-6856-10A-01D-1924-10 | g.chr17:65928032C>T | c.6534C>T | c.(6532-6534)atC>atT | p.I2178I |
| COADREAD | 17 | 65941553 | 65941553 | + | Silent | SNP | G | G | A | TCGA-AA-A00J-01A-02W-A005-10 | TCGA-AA-A00J-10A-01W-A005-10 | g.chr17:65941553G>A | c.7107G>A | c.(7105-7107)ctG>ctA | p.L2369L |
| COADREAD | 17 | 65941738 | 65941738 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3864-01A-01W-0995-10 | TCGA-AA-3864-10A-01W-0995-10 | g.chr17:65941738T>C | c.7292T>C | c.(7291-7293)gTt>gCt | p.V2431A |
| COADREAD | 17 | 65941878 | 65941878 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3555-01A-01W-0831-10 | TCGA-AA-3555-10A-01W-0831-10 | g.chr17:65941878C>T | c.7432C>T | c.(7432-7434)Cgt>Tgt | p.R2478C |
| COADREAD | 17 | 65942230 | 65942230 | + | Missense_Mutation | SNP | T | T | G | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr17:65942230T>G | c.7784T>G | c.(7783-7785)cTc>cGc | p.L2595R |
| COADREAD | 17 | 65942315 | 65942315 | + | Silent | SNP | G | G | A | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr17:65942315G>A | c.7869G>A | c.(7867-7869)gtG>gtA | p.V2623V |
| COADREAD | 17 | 65942392 | 65942392 | + | Missense_Mutation | SNP | G | G | A | TCGA-D5-6928-01A-11D-1924-10 | TCGA-D5-6928-10A-01D-1924-10 | g.chr17:65942392G>A | c.7946G>A | c.(7945-7947)cGt>cAt | p.R2649H |
| COADREAD | 17 | 65943891 | 65943891 | + | Missense_Mutation | SNP | G | G | A | TCGA-CA-5254-01A-21D-1835-10 | TCGA-CA-5254-10A-01D-1835-10 | g.chr17:65943891G>A | c.8045G>A | c.(8044-8046)aGc>aAc | p.S2682N |
| COADREAD | 17 | 65944279 | 65944279 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3977-01A-01W-0995-10 | TCGA-AA-3977-10A-01W-0999-10 | g.chr17:65944279C>T | c.8161C>T | c.(8161-8163)Cgt>Tgt | p.R2721C |
| COADREAD | 17 | 65955870 | 65955870 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3848-01A-01W-0900-09 | TCGA-AA-3848-10A-01W-0900-09 | g.chr17:65955870G>A | c.8518G>A | c.(8518-8520)Gaa>Aaa | p.E2840K |
| COADREAD | 17 | 65971931 | 65971931 | + | Silent | SNP | A | A | G | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr17:65971931A>G | c.8961A>G | c.(8959-8961)gaA>gaG | p.E2987E |
| DLBC | 17 | 65914911 | 65914911 | + | Silent | SNP | T | T | C | TCGA-G8-6324-01A-11D-2210-10 | TCGA-G8-6324-10A-01D-2210-10 | g.chr17:65914911T>C | c.5763T>C | c.(5761-5763)gaT>gaC | p.D1921D |
| DLBC | 17 | 65919092 | 65919092 | + | Silent | SNP | G | G | A | TCGA-G8-6324-01A-11D-2210-10 | TCGA-G8-6324-10A-01D-2210-10 | g.chr17:65919092G>A | c.6072G>A | c.(6070-6072)agG>agA | p.R2024R |
| ESCA | 17 | 65822444 | 65822444 | + | Missense_Mutation | SNP | A | A | G | TCGA-R6-A8WG-01A-11D-A37C-09 | TCGA-R6-A8WG-10A-01D-A37F-09 | g.chr17:65822444A>G | c.604A>G | c.(604-606)Agc>Ggc | p.S202G |
| ESCA | 17 | 65850067 | 65850067 | + | Missense_Mutation | SNP | C | C | G | TCGA-LN-A49X-01A-31D-A27G-09 | TCGA-LN-A49X-10A-01D-A27G-09 | g.chr17:65850067C>G | c.625C>G | c.(625-627)Cca>Gca | p.P209A |
| ESCA | 17 | 65850689 | 65850689 | + | Missense_Mutation | SNP | G | G | T | TCGA-VR-A8ER-01A-11D-A36J-09 | TCGA-VR-A8ER-10A-01D-A36M-09 | g.chr17:65850689G>T | c.1247G>T | c.(1246-1248)tGt>tTt | p.C416F |
| ESCA | 17 | 65905706 | 65905717 | + | In_Frame_Del | DEL | AATATGGATGAA | AATATGGATGAA | - | TCGA-L5-A43I-01A-11D-A247-09 | TCGA-L5-A43I-11A-11D-A247-09 | g.chr17:65905706_65905717delAATATGGATGAA | c.3199_3210delAATATGGATGAA | c.(3199-3210)aatatggatgaadel | p.NMDE1071del |
| ESCA | 17 | 65905779 | 65905779 | + | Missense_Mutation | SNP | C | C | T | TCGA-LN-A4A2-01A-31D-A27G-09 | TCGA-LN-A4A2-10A-01D-A27G-09 | g.chr17:65905779C>T | c.3272C>T | c.(3271-3273)cCt>cTt | p.P1091L |
| ESCA | 17 | 65907999 | 65907999 | + | Missense_Mutation | SNP | G | G | T | TCGA-IC-A6RE-01A-11D-A33E-09 | TCGA-IC-A6RE-10A-01D-A33H-09 | g.chr17:65907999G>T | c.4377G>T | c.(4375-4377)aaG>aaT | p.K1459N |
| ESCA | 17 | 65941986 | 65941986 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-L5-A4OW-01A-11D-A28B-09 | TCGA-L5-A4OW-11A-11D-A28E-09 | g.chr17:65941986C>T | c.7540C>T | c.(7540-7542)Caa>Taa | p.Q2514* |
| ESCA | 17 | 65955782 | 65955783 | + | In_Frame_Ins | INS | - | - | GCC | TCGA-LN-A7HZ-01A-31D-A351-09 | TCGA-LN-A7HZ-10A-01D-A351-09 | g.chr17:65955782_65955783insGCC | c.8430_8431insGCC | c.(8431-8433)cct>GCCcct | p.2810_2811insA |
| ESCA | 17 | 65960430 | 65960430 | + | Missense_Mutation | SNP | G | G | T | TCGA-IG-A4P3-01A-11D-A27G-09 | TCGA-IG-A4P3-10A-01D-A27G-09 | g.chr17:65960430G>T | c.8742G>T | c.(8740-8742)caG>caT | p.Q2914H |
| GBM | 17 | 65862640 | 65862640 | + | Silent | SNP | A | A | G | TCGA-26-1442-01A-01D-1696-08 | TCGA-26-1442-10A-01D-1696-08 | g.chr17:65862640A>G | c.1497A>G | c.(1495-1497)caA>caG | p.Q499Q |
| GBM | 17 | 65888098 | 65888098 | + | Missense_Mutation | SNP | A | A | T | TCGA-41-2575-01A-01D-1495-08 | TCGA-41-2575-10A-01D-1495-08 | g.chr17:65888098A>T | c.2381A>T | c.(2380-2382)cAg>cTg | p.Q794L |
| GBM | 17 | 65889572 | 65889572 | + | Silent | SNP | T | T | C | TCGA-27-2528-01A-01D-1494-08 | TCGA-27-2528-10A-01D-1494-08 | g.chr17:65889572T>C | c.2520T>C | c.(2518-2520)ttT>ttC | p.F840F |
| GBM | 17 | 65889772 | 65889775 | + | Frame_Shift_Del | DEL | GACT | GACT | - | TCGA-12-1597-01B-01D-1495-08 | TCGA-12-1597-10A-01D-1495-08 | g.chr17:65889772_65889775delGACT | c.2720_2723delGACT | c.(2719-2724)agactgfs | p.RL907fs |
| GBM | 17 | 65924656 | 65924656 | + | Silent | SNP | A | A | G | TCGA-76-6193-01A-11D-1696-08 | TCGA-76-6193-10A-01D-1696-08 | g.chr17:65924656A>G | c.6315A>G | c.(6313-6315)caA>caG | p.Q2105Q |
| GBMLGG | 17 | 65850685 | 65850685 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr17:65850685G>A | c.1243G>A | c.(1243-1245)Gaa>Aaa | p.E415K |
| GBMLGG | 17 | 65862640 | 65862640 | + | Silent | SNP | A | A | G | TCGA-26-1442-01A-01D-1696-08 | TCGA-26-1442-10A-01D-1696-08 | g.chr17:65862640A>G | c.1497A>G | c.(1495-1497)caA>caG | p.Q499Q |
| GBMLGG | 17 | 65888098 | 65888098 | + | Missense_Mutation | SNP | A | A | T | TCGA-41-2575-01A-01D-1495-08 | TCGA-41-2575-10A-01D-1495-08 | g.chr17:65888098A>T | c.2381A>T | c.(2380-2382)cAg>cTg | p.Q794L |
| GBMLGG | 17 | 65889572 | 65889572 | + | Silent | SNP | T | T | C | TCGA-27-2528-01A-01D-1494-08 | TCGA-27-2528-10A-01D-1494-08 | g.chr17:65889572T>C | c.2520T>C | c.(2518-2520)ttT>ttC | p.F840F |
| GBMLGG | 17 | 65889772 | 65889775 | + | Frame_Shift_Del | DEL | GACT | GACT | - | TCGA-12-1597-01B-01D-1495-08 | TCGA-12-1597-10A-01D-1495-08 | g.chr17:65889772_65889775delGACT | c.2720_2723delGACT | c.(2719-2724)agactgfs | p.RL907fs |
| GBMLGG | 17 | 65899908 | 65899908 | + | Silent | SNP | A | A | G | TCGA-TQ-A7RJ-01A-11D-A33T-08 | TCGA-TQ-A7RJ-10A-01D-A33W-08 | g.chr17:65899908A>G | c.2925A>G | c.(2923-2925)ttA>ttG | p.L975L |
| GBMLGG | 17 | 65899913 | 65899913 | + | Missense_Mutation | SNP | G | G | A | TCGA-FG-6690-01A-11D-1893-08 | TCGA-FG-6690-10A-01D-1893-08 | g.chr17:65899913G>A | c.2930G>A | c.(2929-2931)cGg>cAg | p.R977Q |
| GBMLGG | 17 | 65908009 | 65908009 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr17:65908009G>T | c.4387G>T | c.(4387-4389)Gtt>Ttt | p.V1463F |
| GBMLGG | 17 | 65909179 | 65909179 | + | Missense_Mutation | SNP | G | G | T | TCGA-HT-A5RB-01A-11D-A289-08 | TCGA-HT-A5RB-10A-01D-A289-08 | g.chr17:65909179G>T | c.5557G>T | c.(5557-5559)Gac>Tac | p.D1853Y |
| GBMLGG | 17 | 65924656 | 65924656 | + | Silent | SNP | A | A | G | TCGA-76-6193-01A-11D-1696-08 | TCGA-76-6193-10A-01D-1696-08 | g.chr17:65924656A>G | c.6315A>G | c.(6313-6315)caA>caG | p.Q2105Q |
| GBMLGG | 17 | 65941667 | 65941667 | + | Silent | SNP | C | C | T | TCGA-QH-A65R-01A-21D-A31L-08 | TCGA-QH-A65R-10A-01D-A31J-08 | g.chr17:65941667C>T | c.7221C>T | c.(7219-7221)ccC>ccT | p.P2407P |
| GBMLGG | 17 | 65955939 | 65955939 | + | Missense_Mutation | SNP | A | A | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr17:65955939A>G | c.8587A>G | c.(8587-8589)Aag>Gag | p.K2863E |
| GBMLGG | 17 | 65978371 | 65978371 | + | Silent | SNP | T | T | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr17:65978371T>A | c.9108T>A | c.(9106-9108)tcT>tcA | p.S3036S |
| HNSC | 17 | 65888058 | 65888058 | + | Missense_Mutation | SNP | C | C | T | TCGA-DQ-5624-01A-01D-1870-08 | TCGA-DQ-5624-10A-01D-1870-08 | g.chr17:65888058C>T | c.2341C>T | c.(2341-2343)Cgg>Tgg | p.R781W |
| HNSC | 17 | 65889610 | 65889610 | + | Missense_Mutation | SNP | A | A | G | TCGA-CQ-6219-01A-11D-1912-08 | TCGA-CQ-6219-10A-01D-1912-08 | g.chr17:65889610A>G | c.2558A>G | c.(2557-2559)aAt>aGt | p.N853S |
| HNSC | 17 | 65905793 | 65905793 | + | Missense_Mutation | SNP | G | G | A | TCGA-BA-6868-01B-12D-1912-08 | TCGA-BA-6868-10A-01D-1912-08 | g.chr17:65905793G>A | c.3286G>A | c.(3286-3288)Gat>Aat | p.D1096N |
| HNSC | 17 | 65907895 | 65907895 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-CV-A6K2-01A-11D-A31L-08 | TCGA-CV-A6K2-10A-01D-A31J-08 | g.chr17:65907895C>T | c.4273C>T | c.(4273-4275)Cag>Tag | p.Q1425* |
| HNSC | 17 | 65909123 | 65909123 | + | Missense_Mutation | SNP | A | A | G | TCGA-UF-A7JA-01A-12D-A34J-08 | TCGA-UF-A7JA-10A-01D-A34M-08 | g.chr17:65909123A>G | c.5501A>G | c.(5500-5502)tAt>tGt | p.Y1834C |
| HNSC | 17 | 65914934 | 65914934 | + | Missense_Mutation | SNP | G | G | T | TCGA-CV-7104-01A-11D-2012-08 | TCGA-CV-7104-10A-01D-2013-08 | g.chr17:65914934G>T | c.5786G>T | c.(5785-5787)gGa>gTa | p.G1929V |
| HNSC | 17 | 65936555 | 65936555 | + | Splice_Site | SNP | G | G | T | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr17:65936555G>T | c.6638G>T | c.(6637-6639)gGt>gTt | p.G2213V |
| KICH | 17 | 65889530 | 65889530 | + | Silent | SNP | C | C | T | TCGA-KN-8418-01A-11D-2310-10 | TCGA-KN-8418-11A-01D-2310-10 | g.chr17:65889530C>T | c.2478C>T | c.(2476-2478)acC>acT | p.T826T |
| KICH | 17 | 65907097 | 65907097 | + | Missense_Mutation | SNP | A | A | G | TCGA-KL-8337-01A-11D-2310-10 | TCGA-KL-8337-11A-01D-2310-10 | g.chr17:65907097A>G | c.3475A>G | c.(3475-3477)Agt>Ggt | p.S1159G |
| KICH | 17 | 65908787 | 65908787 | + | Missense_Mutation | SNP | C | C | T | TCGA-KL-8345-01A-11D-2310-10 | TCGA-KL-8345-11A-01D-2310-10 | g.chr17:65908787C>T | c.5165C>T | c.(5164-5166)gCc>gTc | p.A1722V |
| KICH | 17 | 65909291 | 65909291 | + | Missense_Mutation | SNP | G | G | A | TCGA-KO-8407-01A-11D-2310-10 | TCGA-KO-8407-11A-01D-2311-10 | g.chr17:65909291G>A | c.5669G>A | c.(5668-5670)gGc>gAc | p.G1890D |
| KICH | 17 | 65960371 | 65960371 | + | Missense_Mutation | SNP | C | C | T | TCGA-KO-8411-01A-11D-2310-10 | TCGA-KO-8411-11A-01D-2311-10 | g.chr17:65960371C>T | c.8683C>T | c.(8683-8685)Cgc>Tgc | p.R2895C |
| KIPAN | 17 | 65889530 | 65889530 | + | Silent | SNP | C | C | T | TCGA-KN-8418-01A-11D-2310-10 | TCGA-KN-8418-11A-01D-2310-10 | g.chr17:65889530C>T | c.2478C>T | c.(2476-2478)acC>acT | p.T826T |
| KIPAN | 17 | 65907097 | 65907097 | + | Missense_Mutation | SNP | A | A | G | TCGA-KL-8337-01A-11D-2310-10 | TCGA-KL-8337-11A-01D-2310-10 | g.chr17:65907097A>G | c.3475A>G | c.(3475-3477)Agt>Ggt | p.S1159G |
| KIPAN | 17 | 65908787 | 65908787 | + | Missense_Mutation | SNP | C | C | T | TCGA-KL-8345-01A-11D-2310-10 | TCGA-KL-8345-11A-01D-2310-10 | g.chr17:65908787C>T | c.5165C>T | c.(5164-5166)gCc>gTc | p.A1722V |
| KIPAN | 17 | 65909128 | 65909128 | + | Nonsense_Mutation | SNP | A | A | T | TCGA-B0-4823-01A-02D-1421-08 | TCGA-B0-4823-11A-01D-1421-08 | g.chr17:65909128A>T | c.5506A>T | c.(5506-5508)Aaa>Taa | p.K1836* |
| KIPAN | 17 | 65909291 | 65909291 | + | Missense_Mutation | SNP | G | G | A | TCGA-KO-8407-01A-11D-2310-10 | TCGA-KO-8407-11A-01D-2311-10 | g.chr17:65909291G>A | c.5669G>A | c.(5668-5670)gGc>gAc | p.G1890D |
| KIPAN | 17 | 65916183 | 65916183 | + | Silent | SNP | T | T | C | TCGA-P4-AAVM-01A-11D-A42J-10 | TCGA-P4-AAVM-11A-11D-A42M-10 | g.chr17:65916183T>C | c.5859T>C | c.(5857-5859)gtT>gtC | p.V1953V |
| KIPAN | 17 | 65919081 | 65919082 | + | Frame_Shift_Ins | INS | - | - | G | TCGA-UZ-A9PV-01A-11D-A42J-10 | TCGA-UZ-A9PV-10A-01D-A42M-10 | g.chr17:65919081_65919082insG | c.6061_6062insG | c.(6061-6063)tggfs | p.W2021fs |
| KIPAN | 17 | 65942187 | 65942187 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-CJ-4881-01A-01D-1373-10 | TCGA-CJ-4881-11A-01D-1373-10 | g.chr17:65942187C>T | c.7741C>T | c.(7741-7743)Cag>Tag | p.Q2581* |
| KIPAN | 17 | 65944312 | 65944312 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-UZ-A9PP-01A-11D-A42J-10 | TCGA-UZ-A9PP-10A-01D-A42M-10 | g.chr17:65944312C>T | c.8194C>T | c.(8194-8196)Cag>Tag | p.Q2732* |
| KIPAN | 17 | 65955704 | 65955705 | + | Missense_Mutation | DNP | GC | GC | AG | TCGA-B0-5701-01A-11D-1534-10 | TCGA-B0-5701-11A-01D-1534-10 | g.chr17:65955704_65955705GC>AG | c.8352_8353GC>AG | c.(8350-8355)atGCag>atAGag | p.2784_2785MQ>IE |
| KIPAN | 17 | 65960371 | 65960371 | + | Missense_Mutation | SNP | C | C | T | TCGA-KO-8411-01A-11D-2310-10 | TCGA-KO-8411-11A-01D-2311-10 | g.chr17:65960371C>T | c.8683C>T | c.(8683-8685)Cgc>Tgc | p.R2895C |
| KIPAN | 17 | 65960482 | 65960482 | + | Missense_Mutation | SNP | G | G | C | TCGA-B8-4621-01A-01D-1501-10 | TCGA-B8-4621-10A-01D-1501-10 | g.chr17:65960482G>C | c.8794G>C | c.(8794-8796)Gat>Cat | p.D2932H |
| KIPAN | 17 | 65960510 | 65960510 | + | Missense_Mutation | SNP | G | G | T | TCGA-IA-A40Y-01A-11D-A25F-10 | TCGA-IA-A40Y-10A-01D-A25F-10 | g.chr17:65960510G>T | c.8822G>T | c.(8821-8823)cGt>cTt | p.R2941L |
| KIPAN | 17 | 65972039 | 65972039 | + | Missense_Mutation | SNP | C | C | A | TCGA-B4-5835-01A-11D-1669-08 | TCGA-B4-5835-10A-01D-1669-08 | g.chr17:65972039C>A | c.9069C>A | c.(9067-9069)ttC>ttA | p.F3023L |
| KIRC | 17 | 65909128 | 65909128 | + | Nonsense_Mutation | SNP | A | A | T | TCGA-B0-4823-01A-02D-1421-08 | TCGA-B0-4823-11A-01D-1421-08 | g.chr17:65909128A>T | c.5506A>T | c.(5506-5508)Aaa>Taa | p.K1836* |
| KIRC | 17 | 65942187 | 65942187 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-CJ-4881-01A-01D-1373-10 | TCGA-CJ-4881-11A-01D-1373-10 | g.chr17:65942187C>T | c.7741C>T | c.(7741-7743)Cag>Tag | p.Q2581* |
| KIRC | 17 | 65955704 | 65955705 | + | Missense_Mutation | DNP | GC | GC | AG | TCGA-B0-5701-01A-11D-1534-10 | TCGA-B0-5701-11A-01D-1534-10 | g.chr17:65955704_65955705GC>AG | c.8352_8353GC>AG | c.(8350-8355)atGCag>atAGag | p.2784_2785MQ>IE |
| KIRC | 17 | 65960482 | 65960482 | + | Missense_Mutation | SNP | G | G | C | TCGA-B8-4621-01A-01D-1501-10 | TCGA-B8-4621-10A-01D-1501-10 | g.chr17:65960482G>C | c.8794G>C | c.(8794-8796)Gat>Cat | p.D2932H |
| KIRC | 17 | 65972039 | 65972039 | + | Missense_Mutation | SNP | C | C | A | TCGA-B4-5835-01A-11D-1669-08 | TCGA-B4-5835-10A-01D-1669-08 | g.chr17:65972039C>A | c.9069C>A | c.(9067-9069)ttC>ttA | p.F3023L |
| KIRP | 17 | 65916183 | 65916183 | + | Silent | SNP | T | T | C | TCGA-P4-AAVM-01A-11D-A42J-10 | TCGA-P4-AAVM-11A-11D-A42M-10 | g.chr17:65916183T>C | c.5859T>C | c.(5857-5859)gtT>gtC | p.V1953V |
| KIRP | 17 | 65919081 | 65919082 | + | Frame_Shift_Ins | INS | - | - | G | TCGA-UZ-A9PV-01A-11D-A42J-10 | TCGA-UZ-A9PV-10A-01D-A42M-10 | g.chr17:65919081_65919082insG | c.6061_6062insG | c.(6061-6063)tggfs | p.W2021fs |
| KIRP | 17 | 65944312 | 65944312 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-UZ-A9PP-01A-11D-A42J-10 | TCGA-UZ-A9PP-10A-01D-A42M-10 | g.chr17:65944312C>T | c.8194C>T | c.(8194-8196)Cag>Tag | p.Q2732* |
| KIRP | 17 | 65960510 | 65960510 | + | Missense_Mutation | SNP | G | G | T | TCGA-IA-A40Y-01A-11D-A25F-10 | TCGA-IA-A40Y-10A-01D-A25F-10 | g.chr17:65960510G>T | c.8822G>T | c.(8821-8823)cGt>cTt | p.R2941L |
| LAML | 17 | 65907983 | 65907983 | + | Missense_Mutation | SNP | T | T | G | TCGA-AB-2968-03A-01D-0739-09 | TCGA-AB-2968-11A-01D-0739-09 | g.chr17:65907983T>G | c.4361T>G | c.(4360-4362)gTc>gGc | p.V1454G |
| LGG | 17 | 65850685 | 65850685 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr17:65850685G>A | c.1243G>A | c.(1243-1245)Gaa>Aaa | p.E415K |
| LGG | 17 | 65899908 | 65899908 | + | Silent | SNP | A | A | G | TCGA-TQ-A7RJ-01A-11D-A33T-08 | TCGA-TQ-A7RJ-10A-01D-A33W-08 | g.chr17:65899908A>G | c.2925A>G | c.(2923-2925)ttA>ttG | p.L975L |
| LGG | 17 | 65899913 | 65899913 | + | Missense_Mutation | SNP | G | G | A | TCGA-FG-6690-01A-11D-1893-08 | TCGA-FG-6690-10A-01D-1893-08 | g.chr17:65899913G>A | c.2930G>A | c.(2929-2931)cGg>cAg | p.R977Q |
| LGG | 17 | 65908009 | 65908009 | + | Missense_Mutation | SNP | G | G | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr17:65908009G>T | c.4387G>T | c.(4387-4389)Gtt>Ttt | p.V1463F |
| LGG | 17 | 65909179 | 65909179 | + | Missense_Mutation | SNP | G | G | T | TCGA-HT-A5RB-01A-11D-A289-08 | TCGA-HT-A5RB-10A-01D-A289-08 | g.chr17:65909179G>T | c.5557G>T | c.(5557-5559)Gac>Tac | p.D1853Y |
| LGG | 17 | 65941667 | 65941667 | + | Silent | SNP | C | C | T | TCGA-QH-A65R-01A-21D-A31L-08 | TCGA-QH-A65R-10A-01D-A31J-08 | g.chr17:65941667C>T | c.7221C>T | c.(7219-7221)ccC>ccT | p.P2407P |
| LGG | 17 | 65955939 | 65955939 | + | Missense_Mutation | SNP | A | A | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr17:65955939A>G | c.8587A>G | c.(8587-8589)Aag>Gag | p.K2863E |
| LGG | 17 | 65978371 | 65978371 | + | Silent | SNP | T | T | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr17:65978371T>A | c.9108T>A | c.(9106-9108)tcT>tcA | p.S3036S |
| LIHC | 17 | 65850816 | 65850816 | + | Silent | SNP | T | T | C | TCGA-ES-A2HT-01A-12D-A183-10 | TCGA-ES-A2HT-11A-11D-A183-10 | g.chr17:65850816T>C | c.1374T>C | c.(1372-1374)caT>caC | p.H458H |
| LIHC | 17 | 65862621 | 65862621 | + | Missense_Mutation | SNP | A | A | G | TCGA-4R-AA8I-01A-11D-A382-10 | TCGA-4R-AA8I-10B-01D-A385-10 | g.chr17:65862621A>G | c.1478A>G | c.(1477-1479)tAt>tGt | p.Y493C |
| LIHC | 17 | 65870972 | 65870972 | + | Missense_Mutation | SNP | T | T | C | TCGA-DD-AAD8-01A-11D-A40R-10 | TCGA-DD-AAD8-10A-01D-A40U-10 | g.chr17:65870972T>C | c.1700T>C | c.(1699-1701)aTt>aCt | p.I567T |
| LIHC | 17 | 65871691 | 65871691 | + | Missense_Mutation | SNP | T | T | G | TCGA-DD-AAEA-01A-11D-A40R-10 | TCGA-DD-AAEA-10A-01D-A40U-10 | g.chr17:65871691T>G | c.1884T>G | c.(1882-1884)gaT>gaG | p.D628E |
| LIHC | 17 | 65871699 | 65871699 | + | Missense_Mutation | SNP | A | A | G | TCGA-DD-A1EG-01A-11D-A20W-10 | TCGA-DD-A1EG-10A-01D-A20W-10 | g.chr17:65871699A>G | c.1892A>G | c.(1891-1893)aAc>aGc | p.N631S |
| LIHC | 17 | 65889635 | 65889635 | + | Silent | SNP | T | T | G | TCGA-BC-A10T-01A-11D-A12Z-10 | TCGA-BC-A10T-11A-11D-A12Z-10 | g.chr17:65889635T>G | c.2583T>G | c.(2581-2583)gcT>gcG | p.A861A |
| LIHC | 17 | 65905802 | 65905802 | + | Missense_Mutation | SNP | A | A | G | TCGA-DD-AACM-01A-11D-A40R-10 | TCGA-DD-AACM-10A-01D-A40U-10 | g.chr17:65905802A>G | c.3295A>G | c.(3295-3297)Aaa>Gaa | p.K1099E |
| LIHC | 17 | 65907751 | 65907751 | + | Missense_Mutation | SNP | A | A | G | TCGA-UB-A7MB-01A-11D-A33Q-10 | TCGA-UB-A7MB-10A-01D-A33Q-10 | g.chr17:65907751A>G | c.4129A>G | c.(4129-4131)Agt>Ggt | p.S1377G |
| LIHC | 17 | 65916145 | 65916145 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-WX-AA46-01A-11D-A38X-10 | TCGA-WX-AA46-10A-01D-A38X-10 | g.chr17:65916145G>T | c.5821G>T | c.(5821-5823)Gaa>Taa | p.E1941* |
| LIHC | 17 | 65920661 | 65920661 | + | Splice_Site | SNP | A | A | G | TCGA-2Y-A9H6-01A-11D-A38X-10 | TCGA-2Y-A9H6-10A-01D-A38X-10 | g.chr17:65920661A>G | | c.e17-1 | |
| LIHC | 17 | 65920668 | 65920668 | + | Missense_Mutation | SNP | A | A | G | TCGA-ED-A459-01A-11D-A25V-10 | TCGA-ED-A459-10A-01D-A25V-10 | g.chr17:65920668A>G | c.6092A>G | c.(6091-6093)gAg>gGg | p.E2031G |
| LIHC | 17 | 65924473 | 65924473 | + | Silent | SNP | A | A | G | TCGA-WQ-A9G7-01A-11D-A36X-10 | TCGA-WQ-A9G7-10A-01D-A370-10 | g.chr17:65924473A>G | c.6132A>G | c.(6130-6132)aaA>aaG | p.K2044K |
| LIHC | 17 | 65942113 | 65942113 | + | Missense_Mutation | SNP | C | C | T | TCGA-ES-A2HT-01A-12D-A183-10 | TCGA-ES-A2HT-11A-11D-A183-10 | g.chr17:65942113C>T | c.7667C>T | c.(7666-7668)cCc>cTc | p.P2556L |
| LIHC | 17 | 65955903 | 65955903 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-DD-A39Y-01A-11D-A20W-10 | TCGA-DD-A39Y-11A-11D-A20W-10 | g.chr17:65955903delA | c.8551delA | c.(8551-8553)aaafs | p.K2853fs |
| LIHC | 17 | 65960451 | 65960451 | + | Silent | SNP | C | C | T | TCGA-ES-A2HS-01A-11D-A183-10 | TCGA-ES-A2HS-11A-11D-A183-10 | g.chr17:65960451C>T | c.8763C>T | c.(8761-8763)gcC>gcT | p.A2921A |
| LIHC | 17 | 65971931 | 65971931 | + | Silent | SNP | A | A | G | TCGA-DD-A39X-01A-11D-A20W-10 | TCGA-DD-A39X-11A-11D-A20W-10 | g.chr17:65971931A>G | c.8961A>G | c.(8959-8961)gaA>gaG | p.E2987E |
| LUAD | 17 | 65822303 | 65822303 | + | Missense_Mutation | SNP | A | A | G | TCGA-05-4424-01A-22D-1855-08 | TCGA-05-4424-10A-01D-1855-08 | g.chr17:65822303A>G | c.463A>G | c.(463-465)Acc>Gcc | p.T155A |
| LUAD | 17 | 65822348 | 65822348 | + | Missense_Mutation | SNP | G | G | A | TCGA-17-Z057-01A-01W-0747-08 | TCGA-17-Z057-11A-01W-0747-08 | g.chr17:65822348G>A | c.508G>A | c.(508-510)Gac>Aac | p.D170N |
| LUAD | 17 | 65850086 | 65850086 | + | Missense_Mutation | SNP | G | G | A | TCGA-NJ-A4YQ-01A-11D-A25L-08 | TCGA-NJ-A4YQ-10A-01D-A25L-08 | g.chr17:65850086G>A | c.644G>A | c.(643-645)cGt>cAt | p.R215H |
| LUAD | 17 | 65850144 | 65850144 | + | Missense_Mutation | SNP | G | G | T | TCGA-05-4395-01A-01D-1265-08 | TCGA-05-4395-10A-01D-1265-08 | g.chr17:65850144G>T | c.702G>T | c.(700-702)gaG>gaT | p.E234D |
| LUAD | 17 | 65850461 | 65850461 | + | Missense_Mutation | SNP | A | A | C | TCGA-86-8280-01A-11D-2284-08 | TCGA-86-8280-10A-01D-2284-08 | g.chr17:65850461A>C | c.1019A>C | c.(1018-1020)tAc>tCc | p.Y340S |
| LUAD | 17 | 65850718 | 65850718 | + | Missense_Mutation | SNP | G | G | A | TCGA-78-7542-01A-21D-2063-08 | TCGA-78-7542-11A-01D-2063-08 | g.chr17:65850718G>A | c.1276G>A | c.(1276-1278)Gag>Aag | p.E426K |
| LUAD | 17 | 65850855 | 65850855 | + | Missense_Mutation | SNP | G | G | T | TCGA-55-8302-01A-11D-2323-08 | TCGA-55-8302-10A-01D-2323-08 | g.chr17:65850855G>T | c.1413G>T | c.(1411-1413)tgG>tgT | p.W471C |
| LUAD | 17 | 65850861 | 65850861 | + | Silent | SNP | G | G | A | TCGA-95-7948-01A-11D-2184-08 | TCGA-95-7948-10A-01D-2184-08 | g.chr17:65850861G>A | c.1419G>A | c.(1417-1419)ttG>ttA | p.L473L |
| LUAD | 17 | 65862768 | 65862768 | + | Missense_Mutation | SNP | G | G | A | TCGA-62-8398-01A-11D-2323-08 | TCGA-62-8398-10A-01D-2323-08 | g.chr17:65862768G>A | c.1625G>A | c.(1624-1626)cGg>cAg | p.R542Q |
| LUAD | 17 | 65871138 | 65871139 | + | Splice_Site | INS | - | - | A | TCGA-95-7567-01A-11D-2063-08 | TCGA-95-7567-10A-01D-2063-08 | g.chr17:65871138_65871139insA | | c.e4+2 | |
| LUAD | 17 | 65871746 | 65871746 | + | Missense_Mutation | SNP | G | G | A | TCGA-55-7907-01A-11D-2167-08 | TCGA-55-7907-10A-01D-2167-08 | g.chr17:65871746G>A | c.1939G>A | c.(1939-1941)Gaa>Aaa | p.E647K |
| LUAD | 17 | 65871755 | 65871755 | + | Missense_Mutation | SNP | A | A | G | TCGA-95-7567-01A-11D-2063-08 | TCGA-95-7567-10A-01D-2063-08 | g.chr17:65871755A>G | c.1948A>G | c.(1948-1950)Agt>Ggt | p.S650G |
| LUAD | 17 | 65871764 | 65871764 | + | Missense_Mutation | SNP | G | G | A | TCGA-55-7907-01A-11D-2167-08 | TCGA-55-7907-10A-01D-2167-08 | g.chr17:65871764G>A | c.1957G>A | c.(1957-1959)Gaa>Aaa | p.E653K |
| LUAD | 17 | 65871782 | 65871782 | + | Missense_Mutation | SNP | G | G | T | TCGA-91-6828-01A-11D-1855-08 | TCGA-91-6828-10A-01D-1855-08 | g.chr17:65871782G>T | c.1975G>T | c.(1975-1977)Ggg>Tgg | p.G659W |
| LUAD | 17 | 65871850 | 65871850 | + | Missense_Mutation | SNP | G | G | C | TCGA-55-7907-01A-11D-2167-08 | TCGA-55-7907-10A-01D-2167-08 | g.chr17:65871850G>C | c.2043G>C | c.(2041-2043)caG>caC | p.Q681H |
| LUAD | 17 | 65882262 | 65882262 | + | Missense_Mutation | SNP | G | G | A | TCGA-49-4487-01A-21D-1855-08 | TCGA-49-4487-11A-01D-1855-08 | g.chr17:65882262G>A | c.2072G>A | c.(2071-2073)tGt>tAt | p.C691Y |
| LUAD | 17 | 65887991 | 65887991 | + | Silent | SNP | G | G | T | TCGA-O1-A52J-01A-11D-A25L-08 | TCGA-O1-A52J-10A-01D-A25L-08 | g.chr17:65887991G>T | c.2274G>T | c.(2272-2274)ggG>ggT | p.G758G |
| LUAD | 17 | 65889560 | 65889560 | + | Missense_Mutation | SNP | C | C | G | TCGA-55-8208-01A-11D-2238-08 | TCGA-55-8208-10A-01D-2238-08 | g.chr17:65889560C>G | c.2508C>G | c.(2506-2508)atC>atG | p.I836M |
| LUAD | 17 | 65889808 | 65889808 | + | Missense_Mutation | SNP | C | C | T | TCGA-44-7661-01A-11D-2063-08 | TCGA-44-7661-10A-01D-2063-08 | g.chr17:65889808C>T | c.2756C>T | c.(2755-2757)tCa>tTa | p.S919L |
| LUAD | 17 | 65890174 | 65890174 | + | Missense_Mutation | SNP | G | G | C | TCGA-MP-A4TI-01A-21D-A24P-08 | TCGA-MP-A4TI-10A-01D-A24P-08 | g.chr17:65890174G>C | c.2814G>C | c.(2812-2814)caG>caC | p.Q938H |
| LUAD | 17 | 65907022 | 65907022 | + | Missense_Mutation | SNP | G | G | A | TCGA-17-Z017-01A-01W-0746-08 | TCGA-17-Z017-11A-01W-0746-08 | g.chr17:65907022G>A | c.3400G>A | c.(3400-3402)Gat>Aat | p.D1134N |
| LUAD | 17 | 65907073 | 65907073 | + | Missense_Mutation | SNP | G | G | C | TCGA-86-A4JF-01A-11D-A24P-08 | TCGA-86-A4JF-10A-01D-A24P-08 | g.chr17:65907073G>C | c.3451G>C | c.(3451-3453)Gag>Cag | p.E1151Q |
| LUAD | 17 | 65907073 | 65907073 | + | Missense_Mutation | SNP | G | G | C | TCGA-93-8067-01A-11D-2284-08 | TCGA-93-8067-10A-01D-2284-08 | g.chr17:65907073G>C | c.3451G>C | c.(3451-3453)Gag>Cag | p.E1151Q |
| LUAD | 17 | 65907168 | 65907168 | + | Missense_Mutation | SNP | A | A | T | TCGA-NJ-A4YP-01A-11D-A25L-08 | TCGA-NJ-A4YP-10A-01D-A25L-08 | g.chr17:65907168A>T | c.3546A>T | c.(3544-3546)aaA>aaT | p.K1182N |
| LUAD | 17 | 65907696 | 65907696 | + | Missense_Mutation | SNP | G | G | C | TCGA-86-A4JF-01A-11D-A24P-08 | TCGA-86-A4JF-10A-01D-A24P-08 | g.chr17:65907696G>C | c.4074G>C | c.(4072-4074)aaG>aaC | p.K1358N |
| LUAD | 17 | 65907829 | 65907829 | + | Missense_Mutation | SNP | G | G | A | TCGA-91-8499-01A-11D-2393-08 | TCGA-91-8499-10A-01D-2393-08 | g.chr17:65907829G>A | c.4207G>A | c.(4207-4209)Gga>Aga | p.G1403R |
| LUAD | 17 | 65908725 | 65908725 | + | Silent | SNP | C | C | T | TCGA-93-8067-01A-11D-2284-08 | TCGA-93-8067-10A-01D-2284-08 | g.chr17:65908725C>T | c.5103C>T | c.(5101-5103)gtC>gtT | p.V1701V |
| LUAD | 17 | 65909151 | 65909151 | + | Silent | SNP | G | G | A | TCGA-MN-A4N4-01A-12D-A24P-08 | TCGA-MN-A4N4-10A-01D-A24P-08 | g.chr17:65909151G>A | c.5529G>A | c.(5527-5529)aaG>aaA | p.K1843K |
| LUAD | 17 | 65909301 | 65909301 | + | Missense_Mutation | SNP | G | G | T | TCGA-44-8117-01A-11D-2238-08 | TCGA-44-8117-10A-01D-2238-08 | g.chr17:65909301G>T | c.5679G>T | c.(5677-5679)tgG>tgT | p.W1893C |
| LUAD | 17 | 65920669 | 65920669 | + | Missense_Mutation | SNP | G | G | C | TCGA-55-7994-01A-11D-2184-08 | TCGA-55-7994-10A-01D-2184-08 | g.chr17:65920669G>C | c.6093G>C | c.(6091-6093)gaG>gaC | p.E2031D |
| LUAD | 17 | 65924504 | 65924504 | + | Missense_Mutation | SNP | G | G | A | TCGA-MP-A4T4-01A-11D-A25L-08 | TCGA-MP-A4T4-10A-01D-A25L-08 | g.chr17:65924504G>A | c.6163G>A | c.(6163-6165)Gca>Aca | p.A2055T |
| LUAD | 17 | 65924679 | 65924679 | + | Missense_Mutation | SNP | C | C | T | TCGA-50-6592-01A-11D-1753-08 | TCGA-50-6592-11A-01D-1753-08 | g.chr17:65924679C>T | c.6338C>T | c.(6337-6339)aCc>aTc | p.T2113I |
| LUAD | 17 | 65925581 | 65925581 | + | Missense_Mutation | SNP | G | G | T | TCGA-95-8039-01A-11D-2238-08 | TCGA-95-8039-10A-01D-2238-08 | g.chr17:65925581G>T | c.6506G>T | c.(6505-6507)gGa>gTa | p.G2169V |
| LUAD | 17 | 65928032 | 65928032 | + | Silent | SNP | C | C | T | TCGA-86-8358-01A-11D-2323-08 | TCGA-86-8358-10A-01D-2323-08 | g.chr17:65928032C>T | c.6534C>T | c.(6532-6534)atC>atT | p.I2178I |
| LUAD | 17 | 65928065 | 65928065 | + | Silent | SNP | G | G | C | TCGA-17-Z057-01A-01W-0747-08 | TCGA-17-Z057-11A-01W-0747-08 | g.chr17:65928065G>C | c.6567G>C | c.(6565-6567)gtG>gtC | p.V2189V |
| LUAD | 17 | 65936752 | 65936752 | + | Missense_Mutation | SNP | A | A | G | TCGA-NJ-A4YI-01A-11D-A25L-08 | TCGA-NJ-A4YI-10A-01D-A25L-08 | g.chr17:65936752A>G | c.6835A>G | c.(6835-6837)Act>Gct | p.T2279A |
| LUAD | 17 | 65940369 | 65940369 | + | Missense_Mutation | SNP | A | A | T | TCGA-05-4382-01A-01D-1931-08 | TCGA-05-4382-10A-01D-1265-08 | g.chr17:65940369A>T | c.6959A>T | c.(6958-6960)cAg>cTg | p.Q2320L |
| LUAD | 17 | 65944403 | 65944403 | + | Missense_Mutation | SNP | A | A | T | TCGA-50-7109-01A-11D-2036-08 | TCGA-50-7109-11A-01D-2036-08 | g.chr17:65944403A>T | c.8285A>T | c.(8284-8286)gAt>gTt | p.D2762V |
| LUAD | 17 | 65955973 | 65955973 | + | Missense_Mutation | SNP | C | C | T | TCGA-86-A4JF-01A-11D-A24P-08 | TCGA-86-A4JF-10A-01D-A24P-08 | g.chr17:65955973C>T | c.8621C>T | c.(8620-8622)aCg>aTg | p.T2874M |
| LUAD | 17 | 65962701 | 65962701 | + | Missense_Mutation | SNP | C | C | T | TCGA-86-8073-01A-11D-2238-08 | TCGA-86-8073-10A-01D-2238-08 | g.chr17:65962701C>T | c.8846C>T | c.(8845-8847)gCc>gTc | p.A2949V |
| LUAD | 17 | 65962715 | 65962715 | + | Missense_Mutation | SNP | G | G | C | TCGA-05-4410-01A-21D-1855-08 | TCGA-05-4410-10A-01D-1855-08 | g.chr17:65962715G>C | c.8860G>C | c.(8860-8862)Gaa>Caa | p.E2954Q |
| LUAD | 17 | 65971937 | 65971937 | + | Silent | SNP | G | G | A | TCGA-MP-A4TI-01A-21D-A24P-08 | TCGA-MP-A4TI-10A-01D-A24P-08 | g.chr17:65971937G>A | c.8967G>A | c.(8965-8967)ctG>ctA | p.L2989L |
| LUSC | 17 | 65822267 | 65822267 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-66-2791-01A-01D-0983-08 | TCGA-66-2791-11A-01D-0983-08 | g.chr17:65822267G>T | c.427G>T | c.(427-429)Gag>Tag | p.E143* |
| LUSC | 17 | 65850532 | 65850532 | + | Silent | SNP | C | C | T | TCGA-46-6025-01A-11D-1817-08 | TCGA-46-6025-10A-01D-1817-08 | g.chr17:65850532C>T | c.1090C>T | c.(1090-1092)Cta>Tta | p.L364L |
| LUSC | 17 | 65850849 | 65850849 | + | Missense_Mutation | SNP | A | A | T | TCGA-33-4586-01A-01D-1441-08 | TCGA-33-4586-11A-01D-1441-08 | g.chr17:65850849A>T | c.1407A>T | c.(1405-1407)aaA>aaT | p.K469N |
| LUSC | 17 | 65871037 | 65871037 | + | Missense_Mutation | SNP | G | G | C | TCGA-46-3767-01A-01D-0983-08 | TCGA-46-3767-10A-01D-0983-08 | g.chr17:65871037G>C | c.1765G>C | c.(1765-1767)Gat>Cat | p.D589H |
| LUSC | 17 | 65889712 | 65889712 | + | Missense_Mutation | SNP | G | G | A | TCGA-18-3409-01A-01D-0983-08 | TCGA-18-3409-11A-01D-0983-08 | g.chr17:65889712G>A | c.2660G>A | c.(2659-2661)gGa>gAa | p.G887E |
| LUSC | 17 | 65889725 | 65889725 | + | Missense_Mutation | SNP | G | G | T | TCGA-22-4613-01A-01D-1441-08 | TCGA-22-4613-11A-01D-1441-08 | g.chr17:65889725G>T | c.2673G>T | c.(2671-2673)tgG>tgT | p.W891C |
| LUSC | 17 | 65900897 | 65900897 | + | Missense_Mutation | SNP | G | G | T | TCGA-66-2795-01A-02D-0983-08 | TCGA-66-2795-11A-01D-0983-08 | g.chr17:65900897G>T | c.3131G>T | c.(3130-3132)aGg>aTg | p.R1044M |
| LUSC | 17 | 65907828 | 65907828 | + | Missense_Mutation | SNP | A | A | T | TCGA-22-5482-01A-01D-1632-08 | TCGA-22-5482-11A-01D-1632-08 | g.chr17:65907828A>T | c.4206A>T | c.(4204-4206)gaA>gaT | p.E1402D |
| LUSC | 17 | 65908159 | 65908159 | + | Missense_Mutation | SNP | A | A | G | TCGA-60-2711-01A-01D-1522-08 | TCGA-60-2711-11A-01D-1522-08 | g.chr17:65908159A>G | c.4537A>G | c.(4537-4539)Aaa>Gaa | p.K1513E |
| LUSC | 17 | 65914834 | 65914834 | + | Missense_Mutation | SNP | A | A | G | TCGA-51-4080-01A-01D-1458-08 | TCGA-51-4080-11A-01D-1458-08 | g.chr17:65914834A>G | c.5686A>G | c.(5686-5688)Aga>Gga | p.R1896G |
| LUSC | 17 | 65918974 | 65918974 | + | Missense_Mutation | SNP | G | G | T | TCGA-18-3416-01A-01D-0983-08 | TCGA-18-3416-11A-01D-0983-08 | g.chr17:65918974G>T | c.5954G>T | c.(5953-5955)aGg>aTg | p.R1985M |
| LUSC | 17 | 65918992 | 65918992 | + | Missense_Mutation | SNP | G | G | T | TCGA-22-5473-01A-01D-1632-08 | TCGA-22-5473-11A-11D-1632-08 | g.chr17:65918992G>T | c.5972G>T | c.(5971-5973)aGt>aTt | p.S1991I |
| LUSC | 17 | 65924580 | 65924580 | + | Missense_Mutation | SNP | T | T | G | TCGA-22-5480-01A-01D-1632-08 | TCGA-22-5480-11A-01D-1632-08 | g.chr17:65924580T>G | c.6239T>G | c.(6238-6240)aTa>aGa | p.I2080R |
| LUSC | 17 | 65925453 | 65925453 | + | Splice_Site | SNP | C | C | T | TCGA-22-4613-01A-01D-1441-08 | TCGA-22-4613-11A-01D-1441-08 | g.chr17:65925453C>T | c.6378C>T | c.(6376-6378)ggC>ggT | p.G2126G |
| LUSC | 17 | 65955663 | 65955663 | + | Missense_Mutation | SNP | C | C | A | TCGA-66-2787-01A-01D-0983-08 | TCGA-66-2787-11A-01D-0983-08 | g.chr17:65955663C>A | c.8311C>A | c.(8311-8313)Ctg>Atg | p.L2771M |
| OV | 17 | 65900902 | 65900902 | + | Missense_Mutation | SNP | G | G | C | TCGA-09-2044-01B-01W-0799-08 | TCGA-09-2044-10A-01W-0799-08 | g.chr17:65900902G>C | c.3136G>C | c.(3136-3138)Gtt>Ctt | p.V1046L |
| OV | 17 | 65907750 | 65907750 | + | Missense_Mutation | SNP | G | G | T | TCGA-61-2008-01A-02W-0722-08 | TCGA-61-2008-11A-01W-0722-08 | g.chr17:65907750G>T | c.4128G>T | c.(4126-4128)aaG>aaT | p.K1376N |
| OV | 17 | 65907943 | 65907943 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-13-0792-01A-01W-0370-10 | TCGA-13-0792-10A-01W-0370-10 | g.chr17:65907943delA | c.4321delA | c.(4321-4323)attfs | p.I1441fs |
| OV | 17 | 65920687 | 65920688 | + | Missense_Mutation | DNP | AG | AG | CC | TCGA-24-1469-01A-01W-0553-09 | TCGA-24-1469-10A-01W-0553-09 | g.chr17:65920687_65920688AG>CC | c.6111_6112AG>CC | c.(6109-6114)gcAGtt>gcCCtt | p.V2038L |
| OV | 17 | 65941680 | 65941680 | + | Missense_Mutation | SNP | C | C | G | TCGA-29-1781-01A-01W-0633-09 | TCGA-29-1781-10A-01W-0634-09 | g.chr17:65941680C>G | c.7234C>G | c.(7234-7236)Cag>Gag | p.Q2412E |
| OV | 17 | 65942142 | 65942142 | + | Missense_Mutation | SNP | C | C | A | TCGA-23-2645-01A-01W-1091-09 | TCGA-23-2645-10A-01W-1091-09 | g.chr17:65942142C>A | c.7696C>A | c.(7696-7698)Caa>Aaa | p.Q2566K |
| PAAD | 17 | 65862587 | 65862587 | + | Missense_Mutation | SNP | G | G | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr17:65862587G>T | c.1444G>T | c.(1444-1446)Gat>Tat | p.D482Y |
| PAAD | 17 | 65862593 | 65862593 | + | Missense_Mutation | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr17:65862593G>A | c.1450G>A | c.(1450-1452)Gaa>Aaa | p.E484K |
| PAAD | 17 | 65862768 | 65862768 | + | Missense_Mutation | SNP | G | G | A | TCGA-3A-A9IC-01A-11D-A38G-08 | TCGA-3A-A9IC-10A-01D-A38J-08 | g.chr17:65862768G>A | c.1625G>A | c.(1624-1626)cGg>cAg | p.R542Q |
| PAAD | 17 | 65882284 | 65882284 | + | Silent | SNP | T | T | C | TCGA-IB-AAUR-01A-21D-A38G-08 | TCGA-IB-AAUR-10A-01D-A38J-08 | g.chr17:65882284T>C | c.2094T>C | c.(2092-2094)gcT>gcC | p.A698A |
| PAAD | 17 | 65899951 | 65899951 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-3A-A9IH-01A-12D-A397-08 | TCGA-3A-A9IH-10A-01D-A39A-08 | g.chr17:65899951delA | c.2968delA | c.(2968-2970)aaafs | p.K992fs |
| PAAD | 17 | 65899951 | 65899951 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-HZ-A8P1-01A-11D-A377-08 | TCGA-HZ-A8P1-10A-01D-A37A-08 | g.chr17:65899951delA | c.2968delA | c.(2968-2970)aaafs | p.K992fs |
| PAAD | 17 | 65905755 | 65905755 | + | Missense_Mutation | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr17:65905755G>A | c.3248G>A | c.(3247-3249)aGt>aAt | p.S1083N |
| PAAD | 17 | 65907902 | 65907902 | + | Missense_Mutation | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr17:65907902G>A | c.4280G>A | c.(4279-4281)aGc>aAc | p.S1427N |
| PAAD | 17 | 65924474 | 65924474 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr17:65924474C>T | c.6133C>T | c.(6133-6135)Cga>Tga | p.R2045* |
| PAAD | 17 | 65925454 | 65925454 | + | Missense_Mutation | SNP | G | G | A | TCGA-XD-AAUI-01A-42D-A40W-08 | TCGA-XD-AAUI-10A-01D-A40W-08 | g.chr17:65925454G>A | c.6379G>A | c.(6379-6381)Gtt>Att | p.V2127I |
| PAAD | 17 | 65971920 | 65971920 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr17:65971920C>T | c.8950C>T | c.(8950-8952)Cga>Tga | p.R2984* |
| PCPG | 17 | 65850649 | 65850649 | + | Missense_Mutation | SNP | C | C | T | TCGA-RW-A688-01A-11D-A35D-08 | TCGA-RW-A688-10B-01D-A35B-08 | g.chr17:65850649C>T | c.1207C>T | c.(1207-1209)Ctt>Ttt | p.L403F |
| PCPG | 17 | 65916168 | 65916168 | + | Missense_Mutation | SNP | T | T | G | TCGA-QR-A6H3-01A-11D-A35D-08 | TCGA-QR-A6H3-10A-01D-A35B-08 | g.chr17:65916168T>G | c.5844T>G | c.(5842-5844)atT>atG | p.I1948M |
| PCPG | 17 | 65944414 | 65944414 | + | Missense_Mutation | SNP | G | G | A | TCGA-PR-A5PG-01A-11D-A35D-08 | TCGA-PR-A5PG-10A-01D-A35B-08 | g.chr17:65944414G>A | c.8296G>A | c.(8296-8298)Gaa>Aaa | p.E2766K |
| PRAD | 17 | 65907564 | 65907564 | + | Silent | SNP | C | C | T | TCGA-QU-A6IN-01A-11D-A31L-08 | TCGA-QU-A6IN-10A-01D-A31J-08 | g.chr17:65907564C>T | c.3942C>T | c.(3940-3942)gaC>gaT | p.D1314D |
| PRAD | 17 | 65916199 | 65916199 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-V1-A8WS-01A-11D-A377-08 | TCGA-V1-A8WS-10A-01D-A37A-08 | g.chr17:65916199C>T | c.5875C>T | c.(5875-5877)Cga>Tga | p.R1959* |
| PRAD | 17 | 65940437 | 65940437 | + | Missense_Mutation | SNP | A | A | G | TCGA-HC-A4ZV-01A-11D-A26M-08 | TCGA-HC-A4ZV-10A-01D-A26K-08 | g.chr17:65940437A>G | c.7027A>G | c.(7027-7029)Aca>Gca | p.T2343A |
| PRAD | 17 | 65942002 | 65942002 | + | Missense_Mutation | SNP | C | C | T | TCGA-EJ-7331-01A-11D-2114-08 | TCGA-EJ-7331-10A-01D-2114-08 | g.chr17:65942002C>T | c.7556C>T | c.(7555-7557)tCa>tTa | p.S2519L |
| PRAD | 17 | 65942213 | 65942213 | + | Silent | SNP | G | G | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr17:65942213G>A | c.7767G>A | c.(7765-7767)gtG>gtA | p.V2589V |
| READ | 17 | 65871774 | 65871774 | + | Missense_Mutation | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr17:65871774G>A | c.1967G>A | c.(1966-1968)aGc>aAc | p.S656N |
| READ | 17 | 65890193 | 65890193 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr17:65890193G>T | c.2833G>T | c.(2833-2835)Gaa>Taa | p.E945* |
| READ | 17 | 65900869 | 65900869 | + | Missense_Mutation | SNP | A | A | G | TCGA-DC-6160-01A-11D-1657-10 | TCGA-DC-6160-10A-01D-1657-10 | g.chr17:65900869A>G | c.3103A>G | c.(3103-3105)Agc>Ggc | p.S1035G |
| READ | 17 | 65907077 | 65907077 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr17:65907077C>A | c.3455C>A | c.(3454-3456)tCa>tAa | p.S1152* |
| READ | 17 | 65942230 | 65942230 | + | Missense_Mutation | SNP | T | T | G | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr17:65942230T>G | c.7784T>G | c.(7783-7785)cTc>cGc | p.L2595R |
| SARC | 17 | 65862671 | 65862671 | + | Missense_Mutation | SNP | G | G | A | TCGA-QC-A7B5-01A-11D-A33E-09 | TCGA-QC-A7B5-11A-11D-A33H-09 | g.chr17:65862671G>A | c.1528G>A | c.(1528-1530)Gat>Aat | p.D510N |
| SARC | 17 | 65940483 | 65940483 | + | Missense_Mutation | SNP | C | C | T | TCGA-QC-A7B5-01A-11D-A33E-09 | TCGA-QC-A7B5-11A-11D-A33H-09 | g.chr17:65940483C>T | c.7073C>T | c.(7072-7074)gCa>gTa | p.A2358V |
| SARC | 17 | 65955758 | 65955759 | + | In_Frame_Ins | INS | - | - | CCTCCAGCC | TCGA-DX-A6B9-01A-12D-A32I-09 | TCGA-DX-A6B9-10A-01D-A32I-09 | g.chr17:65955758_65955759insCCTCCAGCC | c.8406_8407insCCTCCAGCC | c.(8407-8409)cct>CCTCCAGCCcct | p.2803_2803P>PPAP |
| SARC | 17 | 65962707 | 65962707 | + | Missense_Mutation | SNP | C | C | T | TCGA-QC-A7B5-01A-11D-A33E-09 | TCGA-QC-A7B5-11A-11D-A33H-09 | g.chr17:65962707C>T | c.8852C>T | c.(8851-8853)cCt>cTt | p.P2951L |
| SKCM | 17 | 65822412 | 65822412 | + | Missense_Mutation | SNP | A | A | T | TCGA-EE-A3JD-06A-11D-A20D-08 | TCGA-EE-A3JD-10A-01D-A20D-08 | g.chr17:65822412A>T | c.572A>T | c.(571-573)gAa>gTa | p.E191V |
| SKCM | 17 | 65850238 | 65850238 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GI-06A-11D-A196-08 | TCGA-EE-A2GI-10A-01D-A198-08 | g.chr17:65850238C>T | c.796C>T | c.(796-798)Cgc>Tgc | p.R266C |
| SKCM | 17 | 65850419 | 65850419 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-DA-A3F5-06A-11D-A20D-08 | TCGA-DA-A3F5-10A-01D-A20D-08 | g.chr17:65850419G>A | c.977G>A | c.(976-978)tGg>tAg | p.W326* |
| SKCM | 17 | 65871076 | 65871076 | + | Missense_Mutation | SNP | C | C | T | TCGA-FS-A1ZC-06A-11D-A197-08 | TCGA-FS-A1ZC-10A-01D-A199-08 | g.chr17:65871076C>T | c.1804C>T | c.(1804-1806)Ctt>Ttt | p.L602F |
| SKCM | 17 | 65871758 | 65871758 | + | Missense_Mutation | SNP | C | C | T | TCGA-GF-A6C9-06A-11D-A30X-08 | TCGA-GF-A6C9-10A-01D-A30X-08 | g.chr17:65871758C>T | c.1951C>T | c.(1951-1953)Ccc>Tcc | p.P651S |
| SKCM | 17 | 65889738 | 65889738 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29N-06A-12D-A197-08 | TCGA-EE-A29N-10A-01D-A199-08 | g.chr17:65889738C>T | c.2686C>T | c.(2686-2688)Cat>Tat | p.H896Y |
| SKCM | 17 | 65890231 | 65890231 | + | Silent | SNP | T | T | C | TCGA-RP-A693-06A-13D-A30X-08 | TCGA-RP-A693-10A-01D-A30X-08 | g.chr17:65890231T>C | c.2871T>C | c.(2869-2871)gtT>gtC | p.V957V |
| SKCM | 17 | 65890239 | 65890239 | + | Missense_Mutation | SNP | T | T | C | TCGA-EE-A3AB-06A-11D-A196-08 | TCGA-EE-A3AB-10A-01D-A198-08 | g.chr17:65890239T>C | c.2879T>C | c.(2878-2880)gTt>gCt | p.V960A |
| SKCM | 17 | 65890259 | 65890259 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-D9-A6E9-06A-12D-A30X-08 | TCGA-D9-A6E9-10A-01D-A30X-08 | g.chr17:65890259C>T | c.2899C>T | c.(2899-2901)Cga>Tga | p.R967* |
| SKCM | 17 | 65899939 | 65899939 | + | Missense_Mutation | SNP | A | A | G | TCGA-EE-A29G-06A-12D-A196-08 | TCGA-EE-A29G-10A-01D-A198-08 | g.chr17:65899939A>G | c.2956A>G | c.(2956-2958)Aag>Gag | p.K986E |
| SKCM | 17 | 65905702 | 65905702 | + | Silent | SNP | A | A | G | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr17:65905702A>G | c.3195A>G | c.(3193-3195)aaA>aaG | p.K1065K |
| SKCM | 17 | 65907066 | 65907066 | + | Missense_Mutation | SNP | G | G | A | TCGA-GF-A6C9-06A-11D-A30X-08 | TCGA-GF-A6C9-10A-01D-A30X-08 | g.chr17:65907066G>A | c.3444G>A | c.(3442-3444)atG>atA | p.M1148I |
| SKCM | 17 | 65907493 | 65907493 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-EE-A3JA-06A-11D-A20D-08 | TCGA-EE-A3JA-10A-01D-A20D-08 | g.chr17:65907493C>T | c.3871C>T | c.(3871-3873)Cga>Tga | p.R1291* |
| SKCM | 17 | 65907642 | 65907642 | + | Silent | SNP | C | C | T | TCGA-EE-A29L-06A-12D-A196-08 | TCGA-EE-A29L-10A-01D-A198-08 | g.chr17:65907642C>T | c.4020C>T | c.(4018-4020)ttC>ttT | p.F1340F |
| SKCM | 17 | 65907666 | 65907666 | + | Missense_Mutation | SNP | T | T | G | TCGA-FS-A1Z3-06A-11D-A197-08 | TCGA-FS-A1Z3-10A-01D-A199-08 | g.chr17:65907666T>G | c.4044T>G | c.(4042-4044)agT>agG | p.S1348R |
| SKCM | 17 | 65907764 | 65907764 | + | Missense_Mutation | SNP | C | C | T | TCGA-GN-A266-06A-11D-A197-08 | TCGA-GN-A266-10A-01D-A199-08 | g.chr17:65907764C>T | c.4142C>T | c.(4141-4143)tCa>tTa | p.S1381L |
| SKCM | 17 | 65908241 | 65908241 | + | Missense_Mutation | SNP | C | C | T | TCGA-FS-A1ZW-06A-12D-A197-08 | TCGA-FS-A1ZW-10A-01D-A199-08 | g.chr17:65908241C>T | c.4619C>T | c.(4618-4620)cCc>cTc | p.P1540L |
| SKCM | 17 | 65908912 | 65908912 | + | Missense_Mutation | SNP | C | C | T | TCGA-FS-A4FC-06A-11D-A24R-08 | TCGA-FS-A4FC-10A-01D-A24R-08 | g.chr17:65908912C>T | c.5290C>T | c.(5290-5292)Ccc>Tcc | p.P1764S |
| SKCM | 17 | 65908943 | 65908943 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2A2-06A-11D-A196-08 | TCGA-EE-A2A2-10A-01D-A198-08 | g.chr17:65908943C>T | c.5321C>T | c.(5320-5322)tCt>tTt | p.S1774F |
| SKCM | 17 | 65909118 | 65909118 | + | Silent | SNP | A | A | G | TCGA-EE-A181-06A-11D-A196-08 | TCGA-EE-A181-10A-01D-A198-08 | g.chr17:65909118A>G | c.5496A>G | c.(5494-5496)ccA>ccG | p.P1832P |
| SKCM | 17 | 65909184 | 65909184 | + | Silent | SNP | A | A | G | TCGA-FS-A4FD-06A-11D-A25O-08 | TCGA-FS-A4FD-10B-01D-A25O-08 | g.chr17:65909184A>G | c.5562A>G | c.(5560-5562)ttA>ttG | p.L1854L |
| SKCM | 17 | 65909211 | 65909211 | + | Silent | SNP | C | C | T | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr17:65909211C>T | c.5589C>T | c.(5587-5589)atC>atT | p.I1863I |
| SKCM | 17 | 65909212 | 65909212 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr17:65909212C>T | c.5590C>T | c.(5590-5592)Cga>Tga | p.R1864* |
| SKCM | 17 | 65909275 | 65909275 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr17:65909275C>T | c.5653C>T | c.(5653-5655)Cct>Tct | p.P1885S |
| SKCM | 17 | 65909276 | 65909276 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr17:65909276C>T | c.5654C>T | c.(5653-5655)cCt>cTt | p.P1885L |
| SKCM | 17 | 65914840 | 65914840 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-EE-A29L-06A-12D-A196-08 | TCGA-EE-A29L-10A-01D-A198-08 | g.chr17:65914840C>T | c.5692C>T | c.(5692-5694)Cag>Tag | p.Q1898* |
| SKCM | 17 | 65914854 | 65914854 | + | Silent | SNP | C | C | T | TCGA-EE-A17X-06A-11D-A197-08 | TCGA-EE-A17X-10A-01D-A199-08 | g.chr17:65914854C>T | c.5706C>T | c.(5704-5706)tcC>tcT | p.S1902S |
| SKCM | 17 | 65914951 | 65914951 | + | Missense_Mutation | SNP | A | A | T | TCGA-GN-A268-06A-11D-A196-08 | TCGA-GN-A268-10A-01D-A198-08 | g.chr17:65914951A>T | c.5803A>T | c.(5803-5805)Aca>Tca | p.T1935S |
| SKCM | 17 | 65928106 | 65928106 | + | Missense_Mutation | SNP | T | T | G | TCGA-ER-A19W-06A-41D-A23B-08 | TCGA-ER-A19W-10A-01D-A23B-08 | g.chr17:65928106T>G | c.6608T>G | c.(6607-6609)aTt>aGt | p.I2203S |
| SKCM | 17 | 65936603 | 65936603 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29M-06A-11D-A196-08 | TCGA-EE-A29M-10A-01D-A198-08 | g.chr17:65936603C>T | c.6686C>T | c.(6685-6687)tCc>tTc | p.S2229F |
| SKCM | 17 | 65940425 | 65940425 | + | Missense_Mutation | SNP | C | C | T | TCGA-DA-A3F3-06A-11D-A20D-08 | TCGA-DA-A3F3-10A-01D-A20D-08 | g.chr17:65940425C>T | c.7015C>T | c.(7015-7017)Cca>Tca | p.P2339S |
| SKCM | 17 | 65941951 | 65941951 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2A1-06A-11D-A197-08 | TCGA-EE-A2A1-10A-01D-A199-08 | g.chr17:65941951C>T | c.7505C>T | c.(7504-7506)cCa>cTa | p.P2502L |
| SKCM | 17 | 65944316 | 65944316 | + | Missense_Mutation | SNP | A | A | G | TCGA-D3-A3MR-06A-11D-A21A-08 | TCGA-D3-A3MR-10A-01D-A21A-08 | g.chr17:65944316A>G | c.8198A>G | c.(8197-8199)aAt>aGt | p.N2733S |
| SKCM | 17 | 65955759 | 65955759 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GJ-06A-11D-A196-08 | TCGA-EE-A2GJ-10A-01D-A198-08 | g.chr17:65955759C>T | c.8407C>T | c.(8407-8409)Cct>Tct | p.P2803S |
| SKCM | 17 | 65972002 | 65972002 | + | Missense_Mutation | SNP | C | C | T | TCGA-FS-A1ZF-06A-12D-A197-08 | TCGA-FS-A1ZF-10A-01D-A199-08 | g.chr17:65972002C>T | c.9032C>T | c.(9031-9033)tCc>tTc | p.S3011F |
| SKCM | 17 | 65972017 | 65972017 | + | Missense_Mutation | SNP | G | G | T | TCGA-EE-A29V-06A-12D-A197-08 | TCGA-EE-A29V-10A-01D-A199-08 | g.chr17:65972017G>T | c.9047G>T | c.(9046-9048)tGt>tTt | p.C3016F |