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 22 41551039 41551039 + Silent SNP T T A TCGA-OR-A5JW-01A-11D-A29I-10 TCGA-OR-A5JW-10A-01D-A29L-10 g.chr22:41551039T>A c.3183T>A c.(3181-3183)acT>acA p.T1061T ACC 22 41568590 41568590 + Missense_Mutation SNP G G A TCGA-OR-A5JB-01A-11D-A29I-10 TCGA-OR-A5JB-10A-01D-A29L-10 g.chr22:41568590G>A c.4540G>A c.(4540-4542)Gaa>Aaa p.E1514K ACC 22 41572252 41572254 + Splice_Site DEL TCT TCT - TCGA-OR-A5LJ-01A-11D-A29I-10 TCGA-OR-A5LJ-10A-01D-A29L-10 g.chr22:41572252_41572254delTCT c.4781_4783delTCT c.(4780-4785)gtcttc>gtc p.F1596del BLCA 22 41489048 41489048 + Missense_Mutation SNP A A C TCGA-BT-A3PH-01A-11D-A21Z-08 TCGA-BT-A3PH-10A-01D-A21Z-08 g.chr22:41489048A>C c.40A>C c.(40-42)Aag>Cag p.K14Q BLCA 22 41489057 41489057 + Missense_Mutation SNP A A G TCGA-CU-A0YR-01A-12D-A10S-08 TCGA-CU-A0YR-10A-01D-A10S-08 g.chr22:41489057A>G c.49A>G c.(49-51)Aaa>Gaa p.K17E BLCA 22 41513203 41513203 + Missense_Mutation SNP T T G TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr22:41513203T>G c.107T>G c.(106-108)cTa>cGa p.L36R BLCA 22 41513289 41513289 + Nonsense_Mutation SNP C C T TCGA-BT-A2LB-01A-11D-A18F-08 TCGA-BT-A2LB-10A-01D-A18F-08 g.chr22:41513289C>T c.193C>T c.(193-195)Cag>Tag p.Q65* BLCA 22 41513680 41513680 + Nonsense_Mutation SNP C C G TCGA-DK-AA6U-01A-11D-A391-08 TCGA-DK-AA6U-10A-01D-A394-08 g.chr22:41513680C>G c.584C>G c.(583-585)tCa>tGa p.S195* BLCA 22 41513766 41513766 + Nonsense_Mutation SNP C C T TCGA-DK-A3WW-01A-22D-A23M-08 TCGA-DK-A3WW-10A-01D-A23K-08 g.chr22:41513766C>T c.670C>T c.(670-672)Cag>Tag p.Q224* BLCA 22 41521961 41521961 + Nonsense_Mutation SNP C C T TCGA-FD-A6TE-01A-12D-A339-08 TCGA-FD-A6TE-10A-21D-A339-08 g.chr22:41521961C>T c.823C>T c.(823-825)Cag>Tag p.Q275* BLCA 22 41523722 41523723 + Frame_Shift_Del DEL AC AC - TCGA-GC-A3BM-01A-11D-A22Z-08 TCGA-GC-A3BM-10A-01D-A22Z-08 g.chr22:41523722_41523723delAC c.1138_1139delAC c.(1138-1140)acafs p.T380fs BLCA 22 41525909 41525909 + Missense_Mutation SNP C C T TCGA-E7-A6MD-01A-41D-A34U-08 TCGA-E7-A6MD-10B-01D-A34X-08 g.chr22:41525909C>T c.1184C>T c.(1183-1185)tCt>tTt p.S395F BLCA 22 41531855 41531855 + Nonsense_Mutation SNP C C T TCGA-GU-AATP-01A-11D-A391-08 TCGA-GU-AATP-10A-01D-A394-08 g.chr22:41531855C>T c.1567C>T c.(1567-1569)Caa>Taa p.Q523* BLCA 22 41536229 41536229 + Nonsense_Mutation SNP G G T TCGA-XF-A9SY-01A-21D-A42E-08 TCGA-XF-A9SY-10A-01D-A42H-08 g.chr22:41536229G>T c.1846G>T c.(1846-1848)Gaa>Taa p.E616* BLCA 22 41537060 41537060 + Nonsense_Mutation SNP C C G TCGA-DK-AA71-01A-31D-A391-08 TCGA-DK-AA71-10A-01D-A394-08 g.chr22:41537060C>G c.1887C>G c.(1885-1887)taC>taG p.Y629* BLCA 22 41537064 41537064 + Missense_Mutation SNP C C G TCGA-GV-A3JZ-01A-11D-A21A-08 TCGA-GV-A3JZ-10A-01D-A21A-08 g.chr22:41537064C>G c.1891C>G c.(1891-1893)Cac>Gac p.H631D BLCA 22 41537115 41537115 + Nonsense_Mutation SNP C C T TCGA-XF-A9T5-01A-11D-A42E-08 TCGA-XF-A9T5-10A-01D-A42H-08 g.chr22:41537115C>T c.1942C>T c.(1942-1944)Cga>Tga p.R648* BLCA 22 41542788 41542788 + Missense_Mutation SNP A A T TCGA-CF-A47Y-01A-11D-A23U-08 TCGA-CF-A47Y-10A-01D-A23U-08 g.chr22:41542788A>T c.2099A>T c.(2098-2100)aAc>aTc p.N700I BLCA 22 41542802 41542802 + Missense_Mutation SNP C C G TCGA-ZF-A9RC-01A-11D-A38G-08 TCGA-ZF-A9RC-10A-01D-A38J-08 g.chr22:41542802C>G c.2113C>G c.(2113-2115)Cga>Gga p.R705G BLCA 22 41543840 41543840 + Splice_Site SNP G G A TCGA-DK-AA77-01A-11D-A391-08 TCGA-DK-AA77-10A-01D-A394-08 g.chr22:41543840G>A c.e12-1 BLCA 22 41545045 41545045 + Missense_Mutation SNP A A G TCGA-G2-A2EJ-01A-11D-A17V-08 TCGA-G2-A2EJ-10A-01D-A17V-08 g.chr22:41545045A>G c.2245A>G c.(2245-2247)Atg>Gtg p.M749V BLCA 22 41545867 41545867 + Missense_Mutation SNP C C T TCGA-FD-A3B8-01A-31D-A20D-08 TCGA-FD-A3B8-10A-01D-A20D-08 g.chr22:41545867C>T c.2482C>T c.(2482-2484)Cat>Tat p.H828Y BLCA 22 41545870 41545870 + Nonsense_Mutation SNP C C T TCGA-FD-A3B8-01A-31D-A20D-08 TCGA-FD-A3B8-10A-01D-A20D-08 g.chr22:41545870C>T c.2485C>T c.(2485-2487)Cag>Tag p.Q829* BLCA 22 41547874 41547874 + Nonsense_Mutation SNP C C G TCGA-2F-A9KR-01A-11D-A38G-08 TCGA-2F-A9KR-10A-01D-A38J-08 g.chr22:41547874C>G c.2855C>G c.(2854-2856)tCa>tGa p.S952* BLCA 22 41547924 41547924 + Nonsense_Mutation SNP G G T TCGA-DK-A3WW-01A-22D-A23M-08 TCGA-DK-A3WW-10A-01D-A23K-08 g.chr22:41547924G>T c.2905G>T c.(2905-2907)Gag>Tag p.E969* BLCA 22 41551076 41551076 + Missense_Mutation SNP C C T TCGA-XF-A9SI-01A-11D-A391-08 TCGA-XF-A9SI-10A-01D-A394-08 g.chr22:41551076C>T c.3220C>T c.(3220-3222)Ccc>Tcc p.P1074S BLCA 22 41551100 41551100 + Nonsense_Mutation SNP C C T TCGA-4Z-AA81-01A-11D-A391-08 TCGA-4Z-AA81-10A-01D-A394-08 g.chr22:41551100C>T c.3244C>T c.(3244-3246)Cag>Tag p.Q1082* BLCA 22 41551100 41551100 + Nonsense_Mutation SNP C C T TCGA-E7-A7XN-01A-11D-A34U-08 TCGA-E7-A7XN-10A-01D-A34X-08 g.chr22:41551100C>T c.3244C>T c.(3244-3246)Cag>Tag p.Q1082* BLCA 22 41551100 41551100 + Nonsense_Mutation SNP C C T TCGA-FD-A6TG-01A-11D-A32B-08 TCGA-FD-A6TG-10A-01D-A329-08 g.chr22:41551100C>T c.3244C>T c.(3244-3246)Cag>Tag p.Q1082* BLCA 22 41551100 41551100 + Nonsense_Mutation SNP C C T TCGA-XF-AAN2-01A-11D-A42E-08 TCGA-XF-AAN2-10A-01D-A42H-08 g.chr22:41551100C>T c.3244C>T c.(3244-3246)Cag>Tag p.Q1082* BLCA 22 41553195 41553195 + Missense_Mutation SNP G G T TCGA-DK-A1A7-01A-11D-A13W-08 TCGA-DK-A1A7-10A-01D-A13W-08 g.chr22:41553195G>T c.3284G>T c.(3283-3285)aGc>aTc p.S1095I BLCA 22 41553245 41553245 + Nonsense_Mutation SNP C C T TCGA-XF-A9SM-01A-11D-A42E-08 TCGA-XF-A9SM-10A-01D-A42H-08 g.chr22:41553245C>T c.3334C>T c.(3334-3336)Cag>Tag p.Q1112* BLCA 22 41553350 41553350 + Nonsense_Mutation SNP G G T TCGA-FJ-A3ZF-01A-11D-A23M-08 TCGA-FJ-A3ZF-10A-01D-A23K-08 g.chr22:41553350G>T c.3439G>T c.(3439-3441)Gag>Tag p.E1147* BLCA 22 41553402 41553402 + Missense_Mutation SNP G G A TCGA-BT-A3PK-01A-21D-A21Z-08 TCGA-BT-A3PK-10A-01D-A21Z-08 g.chr22:41553402G>A c.3491G>A c.(3490-3492)tGt>tAt p.C1164Y BLCA 22 41554442 41554445 + Frame_Shift_Del DEL TTGC TTGC - TCGA-ZF-A9R4-01A-11D-A38G-08 TCGA-ZF-A9R4-10A-01D-A38J-08 g.chr22:41554442_41554445delTTGC c.3528_3531delTTGC c.(3526-3531)tgttgcfs p.CC1176fs BLCA 22 41554476 41554476 + Missense_Mutation SNP G G C TCGA-4Z-AA7Y-01A-11D-A391-08 TCGA-4Z-AA7Y-10A-01D-A394-08 g.chr22:41554476G>C c.3562G>C c.(3562-3564)Gat>Cat p.D1188H BLCA 22 41556657 41556657 + Missense_Mutation SNP G G T TCGA-XF-A9SI-01A-11D-A391-08 TCGA-XF-A9SI-10A-01D-A394-08 g.chr22:41556657G>T c.3602G>T c.(3601-3603)tGt>tTt p.C1201F BLCA 22 41556674 41556674 + Missense_Mutation SNP G G C TCGA-DK-AA6U-01A-11D-A391-08 TCGA-DK-AA6U-10A-01D-A394-08 g.chr22:41556674G>C c.3619G>C c.(3619-3621)Gag>Cag p.E1207Q BLCA 22 41556688 41556688 + Missense_Mutation SNP G G T TCGA-4Z-AA7Y-01A-11D-A391-08 TCGA-4Z-AA7Y-10A-01D-A394-08 g.chr22:41556688G>T c.3633G>T c.(3631-3633)gaG>gaT p.E1211D BLCA 22 41556700 41556700 + Frame_Shift_Del DEL G G - TCGA-E7-A97Q-01A-11D-A38G-08 TCGA-E7-A97Q-10A-01D-A38J-08 g.chr22:41556700delG c.3645delG c.(3643-3645)ttgfs p.L1215fs BLCA 22 41556722 41556722 + Missense_Mutation SNP C C G TCGA-FD-A3SM-01A-11D-A22Z-08 TCGA-FD-A3SM-10A-01D-A22Z-08 g.chr22:41556722C>G c.3667C>G c.(3667-3669)Caa>Gaa p.Q1223E BLCA 22 41560068 41560068 + Missense_Mutation SNP G G T TCGA-FD-A5C0-01A-11D-A289-08 TCGA-FD-A5C0-10A-01D-A289-08 g.chr22:41560068G>T c.3740G>T c.(3739-3741)tGt>tTt p.C1247F BLCA 22 41560092 41560092 + Missense_Mutation SNP A A G TCGA-E7-A678-01A-11D-A30E-08 TCGA-E7-A678-10A-01D-A30H-08 g.chr22:41560092A>G c.3764A>G c.(3763-3765)cAt>cGt p.H1255R BLCA 22 41560132 41560133 + Frame_Shift_Ins INS - - G TCGA-DK-A2I4-01A-11D-A21A-08 TCGA-DK-A2I4-10A-01D-A21A-08 g.chr22:41560132_41560133insG c.3804_3805insG c.(3805-3807)ggafs p.G1269fs BLCA 22 41562613 41562613 + Missense_Mutation SNP G G A TCGA-DK-A2I4-01A-11D-A21A-08 TCGA-DK-A2I4-10A-01D-A21A-08 g.chr22:41562613G>A c.3817G>A c.(3817-3819)Gat>Aat p.D1273N BLCA 22 41564578 41564580 + In_Frame_Del DEL GAA GAA - TCGA-FD-A3SO-01A-11D-A22Z-08 TCGA-FD-A3SO-10A-01D-A22Z-08 g.chr22:41564578_41564580delGAA c.4000_4002delGAA c.(4000-4002)gaadel p.E1334del BLCA 22 41564595 41564595 + Missense_Mutation SNP G G A TCGA-E7-A7DV-01A-11D-A339-08 TCGA-E7-A7DV-10A-01D-A339-08 g.chr22:41564595G>A c.4017G>A c.(4015-4017)atG>atA p.M1339I BLCA 22 41564739 41564739 + Missense_Mutation SNP G G C TCGA-E7-A7DV-01A-11D-A339-08 TCGA-E7-A7DV-10A-01D-A339-08 g.chr22:41564739G>C c.4040G>C c.(4039-4041)gGa>gCa p.G1347A BLCA 22 41564853 41564853 + Missense_Mutation SNP G G A TCGA-GD-A3OQ-01A-32D-A21Z-08 TCGA-GD-A3OQ-10A-01D-A21Z-08 g.chr22:41564853G>A c.4154G>A c.(4153-4155)tGc>tAc p.C1385Y BLCA 22 41564869 41564869 + Missense_Mutation SNP G G C TCGA-E7-A7DV-01A-11D-A339-08 TCGA-E7-A7DV-10A-01D-A339-08 g.chr22:41564869G>C c.4170G>C c.(4168-4170)caG>caC p.Q1390H BLCA 22 41565529 41565529 + Missense_Mutation SNP G G T TCGA-DK-A2I6-01A-12D-A18F-08 TCGA-DK-A2I6-10A-01D-A18F-08 g.chr22:41565529G>T c.4195G>T c.(4195-4197)Gat>Tat p.D1399Y BLCA 22 41565534 41565534 + Missense_Mutation SNP T T G TCGA-UY-A9PB-01A-11D-A38G-08 TCGA-UY-A9PB-10A-01D-A38J-08 g.chr22:41565534T>G c.4200T>G c.(4198-4200)agT>agG p.S1400R BLCA 22 41565561 41565561 + Missense_Mutation SNP G G C TCGA-DK-A1A5-01A-11D-A13W-08 TCGA-DK-A1A5-10A-01D-A13W-08 g.chr22:41565561G>C c.4227G>C c.(4225-4227)ttG>ttC p.L1409F BLCA 22 41565575 41565575 + Missense_Mutation SNP A A G TCGA-FD-A62S-01A-11D-A30E-08 TCGA-FD-A62S-10A-01D-A30H-08 g.chr22:41565575A>G c.4241A>G c.(4240-4242)tAt>tGt p.Y1414C BLCA 22 41565575 41565575 + Missense_Mutation SNP A A G TCGA-ZF-AA58-01A-12D-A42E-08 TCGA-ZF-AA58-10A-01D-A42H-08 g.chr22:41565575A>G c.4241A>G c.(4240-4242)tAt>tGt p.Y1414C BLCA 22 41565601 41565601 + Missense_Mutation SNP G G A TCGA-E7-A7DV-01A-11D-A339-08 TCGA-E7-A7DV-10A-01D-A339-08 g.chr22:41565601G>A c.4267G>A c.(4267-4269)Gaa>Aaa p.E1423K BLCA 22 41565612 41565612 + Silent SNP G G A TCGA-E7-A7DV-01A-11D-A339-08 TCGA-E7-A7DV-10A-01D-A339-08 g.chr22:41565612G>A c.4278G>A c.(4276-4278)aaG>aaA p.K1426K BLCA 22 41566456 41566456 + Missense_Mutation SNP G G A TCGA-E7-A7DV-01A-11D-A339-08 TCGA-E7-A7DV-10A-01D-A339-08 g.chr22:41566456G>A c.4333G>A c.(4333-4335)Gat>Aat p.D1445N BLCA 22 41566487 41566487 + Missense_Mutation SNP A A G TCGA-DK-A3WX-01A-22D-A22Z-08 TCGA-DK-A3WX-10A-01D-A22Z-08 g.chr22:41566487A>G c.4364A>G c.(4363-4365)cAg>cGg p.Q1455R BLCA 22 41566488 41566488 + Missense_Mutation SNP G G C TCGA-G2-A2EL-01A-12D-A18F-08 TCGA-G2-A2EL-10A-01D-A18F-08 g.chr22:41566488G>C c.4365G>C c.(4363-4365)caG>caC p.Q1455H BLCA 22 41566488 41566488 + Silent SNP G G A TCGA-DK-AA6W-01A-12D-A391-08 TCGA-DK-AA6W-10A-01D-A394-08 g.chr22:41566488G>A c.4365G>A c.(4363-4365)caG>caA p.Q1455Q BLCA 22 41568569 41568569 + Missense_Mutation SNP G G A TCGA-ZF-AA51-01A-21D-A391-08 TCGA-ZF-AA51-10A-01D-A394-08 g.chr22:41568569G>A c.4519G>A c.(4519-4521)Gat>Aat p.D1507N BLCA 22 41568577 41568577 + Missense_Mutation SNP G G T TCGA-2F-A9KW-01A-11D-A38G-08 TCGA-2F-A9KW-10A-01D-A38J-08 g.chr22:41568577G>T c.4527G>T c.(4525-4527)tgG>tgT p.W1509C BLCA 22 41568617 41568617 + Nonsense_Mutation SNP G G T TCGA-XF-A9SX-01A-21D-A391-08 TCGA-XF-A9SX-10A-01D-A394-08 g.chr22:41568617G>T c.4567G>T c.(4567-4569)Gag>Tag p.E1523* BLCA 22 41568620 41568620 + Missense_Mutation SNP G G A TCGA-DK-AA6W-01A-12D-A391-08 TCGA-DK-AA6W-10A-01D-A394-08 g.chr22:41568620G>A c.4570G>A c.(4570-4572)Gaa>Aaa p.E1524K BLCA 22 41568628 41568628 + Missense_Mutation SNP G G C TCGA-GV-A3JX-01A-11D-A20D-08 TCGA-GV-A3JX-10A-01D-A20D-08 g.chr22:41568628G>C c.4578G>C c.(4576-4578)gaG>gaC p.E1526D BLCA 22 41568639 41568639 + Frame_Shift_Del DEL A A - TCGA-DK-AA6M-01A-11D-A391-08 TCGA-DK-AA6M-10A-01D-A394-08 g.chr22:41568639delA c.4589delA c.(4588-4590)gagfs p.E1531fs BLCA 22 41569659 41569659 + Missense_Mutation SNP G G T TCGA-E7-A7DV-01A-11D-A339-08 TCGA-E7-A7DV-10A-01D-A339-08 g.chr22:41569659G>T c.4650G>T c.(4648-4650)aaG>aaT p.K1550N BLCA 22 41569698 41569698 + Silent SNP G G C TCGA-E7-A7DV-01A-11D-A339-08 TCGA-E7-A7DV-10A-01D-A339-08 g.chr22:41569698G>C c.4689G>C c.(4687-4689)ctG>ctC p.L1563L BLCA 22 41569739 41569739 + Missense_Mutation SNP C C T TCGA-ZF-AA4V-01A-11D-A38G-08 TCGA-ZF-AA4V-10A-01D-A38J-08 g.chr22:41569739C>T c.4730C>T c.(4729-4731)tCt>tTt p.S1577F BLCA 22 41572327 41572327 + Missense_Mutation SNP T T C TCGA-E7-A6MD-01A-41D-A34U-08 TCGA-E7-A6MD-10B-01D-A34X-08 g.chr22:41572327T>C c.4856T>C c.(4855-4857)aTc>aCc p.I1619T BLCA 22 41572350 41572350 + Missense_Mutation SNP C C G TCGA-ZF-A9R5-01A-12D-A42E-08 TCGA-ZF-A9R5-10A-01D-A42H-08 g.chr22:41572350C>G c.4879C>G c.(4879-4881)Cgg>Ggg p.R1627G BLCA 22 41572402 41572403 + Frame_Shift_Ins INS - - C TCGA-FT-A61P-01A-11D-A30E-08 TCGA-FT-A61P-10A-01D-A30H-08 g.chr22:41572402_41572403insC c.4931_4932insC c.(4930-4935)ctccgafs p.R1645fs BLCA 22 41572404 41572404 + Nonsense_Mutation SNP C C T TCGA-CU-A3KJ-01A-11D-A21A-08 TCGA-CU-A3KJ-10A-01D-A21A-08 g.chr22:41572404C>T c.4933C>T c.(4933-4935)Cga>Tga p.R1645* BLCA 22 41572411 41572411 + Frame_Shift_Del DEL C C - TCGA-GC-A3RB-01A-12D-A21Z-08 TCGA-GC-A3RB-10A-01D-A21Z-08 g.chr22:41572411delC c.4940delC c.(4939-4941)gccfs p.A1647fs BLCA 22 41572932 41572932 + Missense_Mutation SNP C C G TCGA-CU-A3KJ-01A-11D-A21A-08 TCGA-CU-A3KJ-10A-01D-A21A-08 g.chr22:41572932C>G c.5217C>G c.(5215-5217)atC>atG p.I1739M BLCA 22 41573079 41573079 + Silent SNP C C G TCGA-CU-A3KJ-01A-11D-A21A-08 TCGA-CU-A3KJ-10A-01D-A21A-08 g.chr22:41573079C>G c.5364C>G c.(5362-5364)ctC>ctG p.L1788L BLCA 22 41573148 41573148 + Missense_Mutation SNP G G T TCGA-DK-A3WW-01A-22D-A23M-08 TCGA-DK-A3WW-10A-01D-A23K-08 g.chr22:41573148G>T c.5433G>T c.(5431-5433)caG>caT p.Q1811H BLCA 22 41573719 41573719 + Missense_Mutation SNP C C G TCGA-CU-A3KJ-01A-11D-A21A-08 TCGA-CU-A3KJ-10A-01D-A21A-08 g.chr22:41573719C>G c.6004C>G c.(6004-6006)Cag>Gag p.Q2002E BLCA 22 41573838 41573838 + Silent SNP C C G TCGA-CU-A3KJ-01A-11D-A21A-08 TCGA-CU-A3KJ-10A-01D-A21A-08 g.chr22:41573838C>G c.6123C>G c.(6121-6123)ctC>ctG p.L2041L BLCA 22 41573889 41573889 + Silent SNP C C G TCGA-CU-A3KJ-01A-11D-A21A-08 TCGA-CU-A3KJ-10A-01D-A21A-08 g.chr22:41573889C>G c.6174C>G c.(6172-6174)ctC>ctG p.L2058L BLCA 22 41573897 41573897 + Missense_Mutation SNP C C T TCGA-UY-A9PE-01A-11D-A38G-08 TCGA-UY-A9PE-10A-01D-A38J-08 g.chr22:41573897C>T c.6182C>T c.(6181-6183)cCc>cTc p.P2061L BLCA 22 41574076 41574076 + Nonsense_Mutation SNP C C T TCGA-K4-A54R-01A-11D-A26M-08 TCGA-K4-A54R-10A-01D-A26K-08 g.chr22:41574076C>T c.6361C>T c.(6361-6363)Cag>Tag p.Q2121* BLCA 22 41574216 41574216 + Silent SNP G G A TCGA-E7-A7XN-01A-11D-A34U-08 TCGA-E7-A7XN-10A-01D-A34X-08 g.chr22:41574216G>A c.6501G>A c.(6499-6501)caG>caA p.Q2167Q BLCA 22 41574279 41574279 + Missense_Mutation SNP G G A TCGA-DK-AA71-01A-31D-A391-08 TCGA-DK-AA71-10A-01D-A394-08 g.chr22:41574279G>A c.6564G>A c.(6562-6564)atG>atA p.M2188I BLCA 22 41574314 41574314 + Missense_Mutation SNP G G C TCGA-DK-AA71-01A-31D-A391-08 TCGA-DK-AA71-10A-01D-A394-08 g.chr22:41574314G>C c.6599G>C c.(6598-6600)gGa>gCa p.G2200A BLCA 22 41574469 41574469 + Nonsense_Mutation SNP G G T TCGA-BT-A20X-01A-11D-A16O-08 TCGA-BT-A20X-11A-12D-A16O-08 g.chr22:41574469G>T c.6754G>T c.(6754-6756)Gag>Tag p.E2252* BLCA 22 41574921 41574921 + Missense_Mutation SNP G G C TCGA-R3-A69X-01A-22D-A30E-08 TCGA-R3-A69X-10A-01D-A30H-08 g.chr22:41574921G>C c.7206G>C c.(7204-7206)ttG>ttC p.L2402F BRCA 22 41489026 41489026 + Silent SNP G G A TCGA-BH-A18U-01A-21D-A12B-09 TCGA-BH-A18U-11A-23D-A12B-09 g.chr22:41489026G>A c.18G>A c.(16-18)gtG>gtA p.V6V BRCA 22 41521913 41521913 + Nonsense_Mutation SNP C C T TCGA-GM-A2DL-01A-11D-A18P-09 TCGA-GM-A2DL-10C-01D-A18P-09 g.chr22:41521913C>T c.775C>T c.(775-777)Cag>Tag p.Q259* BRCA 22 41523564 41523564 + Missense_Mutation SNP C C T TCGA-D8-A1XZ-01A-11D-A14K-09 TCGA-D8-A1XZ-10A-01D-A14K-09 g.chr22:41523564C>T c.980C>T c.(979-981)gCa>gTa p.A327V BRCA 22 41527458 41527458 + Missense_Mutation SNP C C T TCGA-BH-A0HF-01A-11W-A071-09 TCGA-BH-A0HF-10A-01W-A071-09 g.chr22:41527458C>T c.1349C>T c.(1348-1350)gCc>gTc p.A450V BRCA 22 41527549 41527549 + Missense_Mutation SNP G G A TCGA-EW-A423-01A-11D-A243-09 TCGA-EW-A423-10A-01D-A243-09 g.chr22:41527549G>A c.1440G>A c.(1438-1440)atG>atA p.M480I BRCA 22 41527610 41527611 + Frame_Shift_Ins INS - - G TCGA-E9-A1N3-01A-12D-A159-09 TCGA-E9-A1N3-10A-01D-A159-09 g.chr22:41527610_41527611insG c.1501_1502insG c.(1501-1503)caafs p.Q501fs BRCA 22 41545099 41545099 + Nonsense_Mutation SNP C C T TCGA-A8-A0A7-01A-11W-A019-09 TCGA-A8-A0A7-10A-01W-A021-09 g.chr22:41545099C>T c.2299C>T c.(2299-2301)Cag>Tag p.Q767* BRCA 22 41545883 41545883 + Missense_Mutation SNP C C T TCGA-D8-A1XM-01A-21D-A14K-09 TCGA-D8-A1XM-10A-01D-A14K-09 g.chr22:41545883C>T c.2498C>T c.(2497-2499)tCg>tTg p.S833L BRCA 22 41564860 41564860 + Silent SNP A A C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr22:41564860A>C c.4161A>C c.(4159-4161)ccA>ccC p.P1387P BRCA 22 41566475 41566475 + Missense_Mutation SNP A A C TCGA-C8-A27B-01A-11D-A167-09 TCGA-C8-A27B-10A-01D-A167-09 g.chr22:41566475A>C c.4352A>C c.(4351-4353)cAt>cCt p.H1451P BRCA 22 41566525 41566525 + Frame_Shift_Del DEL A A - TCGA-BH-A18G-01A-11D-A12B-09 TCGA-BH-A18G-10A-01D-A12B-09 g.chr22:41566525delA c.4402delA c.(4402-4404)aaafs p.K1469fs BRCA 22 41568658 41568658 + Missense_Mutation SNP A A T TCGA-D8-A1XK-01A-21D-A14K-09 TCGA-D8-A1XK-10A-01D-A14K-09 g.chr22:41568658A>T c.4608A>T c.(4606-4608)gaA>gaT p.E1536D BRCA 22 41572386 41572386 + Silent SNP C C T TCGA-A7-A4SA-01A-11D-A25Q-09 TCGA-A7-A4SA-10A-01D-A25Q-09 g.chr22:41572386C>T c.4915C>T c.(4915-4917)Ctg>Ttg p.L1639L BRCA 22 41573243 41573243 + Missense_Mutation SNP A A C TCGA-A2-A0T5-01A-21D-A099-09 TCGA-A2-A0T5-10A-01D-A099-09 g.chr22:41573243A>C c.5528A>C c.(5527-5529)cAg>cCg p.Q1843P BRCA 22 41573463 41573463 + Silent SNP A A C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr22:41573463A>C c.5748A>C c.(5746-5748)ccA>ccC p.P1916P BRCA 22 41573569 41573569 + Missense_Mutation SNP A A G TCGA-BH-A18G-01A-11D-A12B-09 TCGA-BH-A18G-10A-01D-A12B-09 g.chr22:41573569A>G c.5854A>G c.(5854-5856)Atc>Gtc p.I1952V BRCA 22 41573738 41573738 + Missense_Mutation SNP C C T TCGA-BH-A0DZ-01A-11W-A019-09 TCGA-BH-A0DZ-10A-01W-A021-09 g.chr22:41573738C>T c.6023C>T c.(6022-6024)tCt>tTt p.S2008F CESC 22 41489064 41489064 + Nonsense_Mutation SNP C C G TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr22:41489064C>G c.56C>G c.(55-57)tCa>tGa p.S19* CESC 22 41521980 41521980 + Nonsense_Mutation SNP C C G TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr22:41521980C>G c.842C>G c.(841-843)tCa>tGa p.S281* CESC 22 41523536 41523536 + Missense_Mutation SNP C C G TCGA-JX-A3Q0-01A-11D-A21Q-09 TCGA-JX-A3Q0-10A-01D-A21Q-09 g.chr22:41523536C>G c.952C>G c.(952-954)Cca>Gca p.P318A CESC 22 41525927 41525927 + Nonsense_Mutation SNP C C G TCGA-C5-A1MH-01A-11D-A14W-08 TCGA-C5-A1MH-10A-01D-A14W-08 g.chr22:41525927C>G c.1202C>G c.(1201-1203)tCa>tGa p.S401* CESC 22 41527552 41527552 + Silent SNP G G A TCGA-FU-A3HZ-01A-11D-A20U-09 TCGA-FU-A3HZ-10A-01D-A20U-09 g.chr22:41527552G>A c.1443G>A c.(1441-1443)ccG>ccA p.P481P CESC 22 41533715 41533715 + Nonsense_Mutation SNP C C T TCGA-EK-A2R8-01A-21D-A18J-09 TCGA-EK-A2R8-10A-01D-A18J-09 g.chr22:41533715C>T c.1681C>T c.(1681-1683)Caa>Taa p.Q561* CESC 22 41537053 41537053 + Splice_Site SNP C C T TCGA-EA-A3HU-01A-11D-A20U-09 TCGA-EA-A3HU-10B-01D-A20U-09 g.chr22:41537053C>T c.1880C>T c.(1879-1881)gCg>gTg p.A627V CESC 22 41537115 41537115 + Nonsense_Mutation SNP C C T TCGA-EA-A3HQ-01A-11D-A20U-09 TCGA-EA-A3HQ-10A-01D-A20U-09 g.chr22:41537115C>T c.1942C>T c.(1942-1944)Cga>Tga p.R648* CESC 22 41543930 41543930 + Nonsense_Mutation SNP C C T TCGA-JX-A3Q0-01A-11D-A21Q-09 TCGA-JX-A3Q0-10A-01D-A21Q-09 g.chr22:41543930C>T c.2221C>T c.(2221-2223)Caa>Taa p.Q741* CESC 22 41545129 41545129 + Missense_Mutation SNP G G A TCGA-MY-A5BD-01A-11D-A26G-09 TCGA-MY-A5BD-10A-01D-A26G-09 g.chr22:41545129G>A c.2329G>A c.(2329-2331)Gta>Ata p.V777I CESC 22 41545822 41545822 + Nonsense_Mutation SNP C C T TCGA-EK-A2RK-01A-11D-A18J-09 TCGA-EK-A2RK-10A-01D-A18J-09 g.chr22:41545822C>T c.2437C>T c.(2437-2439)Cag>Tag p.Q813* CESC 22 41547874 41547874 + Nonsense_Mutation SNP C C G TCGA-LP-A5U2-01A-11D-A28B-09 TCGA-LP-A5U2-10A-01D-A28E-09 g.chr22:41547874C>G c.2855C>G c.(2854-2856)tCa>tGa p.S952* CESC 22 41556727 41556727 + Splice_Site SNP G G A TCGA-FU-A3TQ-01A-11D-A22X-09 TCGA-FU-A3TQ-10A-01D-A22X-09 g.chr22:41556727G>A c.e20+1 CESC 22 41558764 41558764 + Missense_Mutation SNP G G T TCGA-C5-A7UH-01A-11D-A351-09 TCGA-C5-A7UH-10A-01D-A351-09 g.chr22:41558764G>T c.3709G>T c.(3709-3711)Gac>Tac p.D1237Y CESC 22 41562602 41562602 + Splice_Site SNP G G C TCGA-LP-A5U2-01A-11D-A28B-09 TCGA-LP-A5U2-10A-01D-A28E-09 g.chr22:41562602G>C c.e23-1 CESC 22 41562645 41562645 + Missense_Mutation SNP G G T TCGA-EK-A2PM-01A-11D-A18J-09 TCGA-EK-A2PM-10A-01D-A18J-09 g.chr22:41562645G>T c.3849G>T c.(3847-3849)agG>agT p.R1283S CESC 22 41564513 41564513 + Missense_Mutation SNP G G A TCGA-EA-A3QD-01A-32D-A22X-09 TCGA-EA-A3QD-10A-01D-A22X-09 g.chr22:41564513G>A c.3935G>A c.(3934-3936)cGa>cAa p.R1312Q CESC 22 41565529 41565529 + Missense_Mutation SNP G G A TCGA-C5-A7CG-01A-11D-A32I-09 TCGA-C5-A7CG-10A-01D-A32I-09 g.chr22:41565529G>A c.4195G>A c.(4195-4197)Gat>Aat p.D1399N CESC 22 41565529 41565529 + Missense_Mutation SNP G G A TCGA-EA-A5O9-01A-11D-A28B-09 TCGA-EA-A5O9-10A-01D-A28E-09 g.chr22:41565529G>A c.4195G>A c.(4195-4197)Gat>Aat p.D1399N CESC 22 41565529 41565529 + Missense_Mutation SNP G G A TCGA-EX-A1H5-01A-31D-A13W-08 TCGA-EX-A1H5-10A-01D-A13W-08 g.chr22:41565529G>A c.4195G>A c.(4195-4197)Gat>Aat p.D1399N CESC 22 41565529 41565529 + Missense_Mutation SNP G G A TCGA-JW-A852-01A-11D-A351-09 TCGA-JW-A852-10A-01D-A351-09 g.chr22:41565529G>A c.4195G>A c.(4195-4197)Gat>Aat p.D1399N CESC 22 41565529 41565529 + Missense_Mutation SNP G G A TCGA-MY-A5BE-01A-21D-A26G-09 TCGA-MY-A5BE-10A-01D-A26G-09 g.chr22:41565529G>A c.4195G>A c.(4195-4197)Gat>Aat p.D1399N CESC 22 41569751 41569751 + Missense_Mutation SNP C C T TCGA-FU-A3HY-01A-11D-A21Q-09 TCGA-FU-A3HY-10A-01D-A21Q-09 g.chr22:41569751C>T c.4742C>T c.(4741-4743)tCa>tTa p.S1581L CESC 22 41572405 41572405 + Missense_Mutation SNP G G A TCGA-C5-A7UH-01A-11D-A351-09 TCGA-C5-A7UH-10A-01D-A351-09 g.chr22:41572405G>A c.4934G>A c.(4933-4935)cGa>cAa p.R1645Q CESC 22 41572870 41572870 + Nonsense_Mutation SNP C C T TCGA-FU-A3NI-01A-11D-A21Q-09 TCGA-FU-A3NI-10A-01D-A21Q-09 g.chr22:41572870C>T c.5155C>T c.(5155-5157)Cag>Tag p.Q1719* CESC 22 41574358 41574358 + Nonsense_Mutation SNP C C T TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chr22:41574358C>T c.6643C>T c.(6643-6645)Caa>Taa p.Q2215* CESC 22 41574469 41574469 + Nonsense_Mutation SNP G G T TCGA-JX-A3Q0-01A-11D-A21Q-09 TCGA-JX-A3Q0-10A-01D-A21Q-09 g.chr22:41574469G>T c.6754G>T c.(6754-6756)Gag>Tag p.E2252* CHOL 22 41513219 41513219 + Missense_Mutation SNP C C G TCGA-W5-AA39-01A-11D-A417-09 TCGA-W5-AA39-10A-01D-A41A-09 g.chr22:41513219C>G c.123C>G c.(121-123)caC>caG p.H41Q CHOL 22 41547849 41547849 + Missense_Mutation SNP G G A TCGA-W5-AA2O-01A-11D-A417-09 TCGA-W5-AA2O-10A-01D-A41A-09 g.chr22:41547849G>A c.2830G>A c.(2830-2832)Gct>Act p.A944T CHOL 22 41574848 41574848 + Missense_Mutation SNP G G A TCGA-W5-AA39-01A-11D-A417-09 TCGA-W5-AA39-10A-01D-A41A-09 g.chr22:41574848G>A c.7133G>A c.(7132-7134)aGc>aAc p.S2378N COAD 22 41513284 41513284 + Missense_Mutation SNP A A G TCGA-A6-5659-01A-01D-1650-10 TCGA-A6-5659-11A-01D-1650-10 g.chr22:41513284A>G c.188A>G c.(187-189)cAg>cGg p.Q63R COAD 22 41513293 41513293 + Missense_Mutation SNP C C T TCGA-AA-3554-01A-01W-0833-10 TCGA-AA-3554-10A-01W-0833-10 g.chr22:41513293C>T c.197C>T c.(196-198)aCa>aTa p.T66I COAD 22 41513347 41513347 + Missense_Mutation SNP T T C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr22:41513347T>C c.251T>C c.(250-252)tTg>tCg p.L84S COAD 22 41513353 41513353 + Missense_Mutation SNP G G A TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr22:41513353G>A c.257G>A c.(256-258)cGa>cAa p.R86Q COAD 22 41513353 41513353 + Missense_Mutation SNP G G A TCGA-CM-4752-01A-01D-1408-10 TCGA-CM-4752-10A-01D-1408-10 g.chr22:41513353G>A c.257G>A c.(256-258)cGa>cAa p.R86Q COAD 22 41513474 41513474 + Missense_Mutation SNP G G A TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr22:41513474G>A c.378G>A c.(376-378)atG>atA p.M126I COAD 22 41513540 41513540 + Silent SNP G G A TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr22:41513540G>A c.444G>A c.(442-444)acG>acA p.T148T COAD 22 41513675 41513675 + Silent SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr22:41513675C>T c.579C>T c.(577-579)aaC>aaT p.N193N COAD 22 41523729 41523729 + Missense_Mutation SNP G G A TCGA-AA-A01G-01A-01W-A005-10 TCGA-AA-A01G-10A-01W-A005-10 g.chr22:41523729G>A c.1145G>A c.(1144-1146)tGc>tAc p.C382Y COAD 22 41525931 41525931 + Silent SNP C C T TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr22:41525931C>T c.1206C>T c.(1204-1206)caC>caT p.H402H COAD 22 41527630 41527630 + Silent SNP C C T TCGA-AY-5543-01A-01D-1650-10 TCGA-AY-5543-10A-01D-1650-10 g.chr22:41527630C>T c.1521C>T c.(1519-1521)agC>agT p.S507S COAD 22 41527630 41527630 + Silent SNP C C T TCGA-CM-6166-01A-11D-1650-10 TCGA-CM-6166-10A-01D-1650-10 g.chr22:41527630C>T c.1521C>T c.(1519-1521)agC>agT p.S507S COAD 22 41531883 41531883 + Missense_Mutation SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr22:41531883T>G c.1595T>G c.(1594-1596)aTg>aGg p.M532R COAD 22 41533736 41533736 + Missense_Mutation SNP C C T TCGA-AA-3555-01A-01W-0831-10 TCGA-AA-3555-10A-01W-0831-10 g.chr22:41533736C>T c.1702C>T c.(1702-1704)Cgg>Tgg p.R568W COAD 22 41533773 41533773 + Missense_Mutation SNP G G A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr22:41533773G>A c.1739G>A c.(1738-1740)cGa>cAa p.R580Q COAD 22 41533773 41533773 + Missense_Mutation SNP G G A TCGA-D5-6920-01A-11D-1924-10 TCGA-D5-6920-10A-01D-1924-10 g.chr22:41533773G>A c.1739G>A c.(1738-1740)cGa>cAa p.R580Q COAD 22 41533793 41533793 + Splice_Site SNP C C T TCGA-D5-6931-01A-11D-1924-10 TCGA-D5-6931-10A-01D-1924-10 g.chr22:41533793C>T c.1759C>T c.(1759-1761)Ctc>Ttc p.L587F COAD 22 41536153 41536153 + Silent SNP C C T TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr22:41536153C>T c.1770C>T c.(1768-1770)gcC>gcT p.A590A COAD 22 41536167 41536167 + Missense_Mutation SNP C C T TCGA-CA-5796-01A-01D-1650-10 TCGA-CA-5796-10A-01D-1650-10 g.chr22:41536167C>T c.1784C>T c.(1783-1785)cCg>cTg p.P595L COAD 22 41536193 41536193 + Missense_Mutation SNP C C G TCGA-AA-3527-01A-01W-0831-10 TCGA-AA-3527-10A-01W-0831-10 g.chr22:41536193C>G c.1810C>G c.(1810-1812)Cgg>Ggg p.R604G COAD 22 41545847 41545847 + Missense_Mutation SNP A A G TCGA-AA-3662-01A-01D-1719-10 TCGA-AA-3662-11A-01D-1719-10 g.chr22:41545847A>G c.2462A>G c.(2461-2463)cAg>cGg p.Q821R COAD 22 41545897 41545897 + Missense_Mutation SNP C C T TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr22:41545897C>T c.2512C>T c.(2512-2514)Cgt>Tgt p.R838C COAD 22 41547864 41547864 + Nonsense_Mutation SNP G G T TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr22:41547864G>T c.2845G>T c.(2845-2847)Gga>Tga p.G949* COAD 22 41548250 41548250 + Missense_Mutation SNP A A G TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr22:41548250A>G c.3038A>G c.(3037-3039)gAa>gGa p.E1013G COAD 22 41548251 41548251 + Silent SNP A A G TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr22:41548251A>G c.3039A>G c.(3037-3039)gaA>gaG p.E1013E COAD 22 41548251 41548251 + Silent SNP A A G TCGA-D5-6533-01A-11D-1719-10 TCGA-D5-6533-10A-01D-1719-10 g.chr22:41548251A>G c.3039A>G c.(3037-3039)gaA>gaG p.E1013E COAD 22 41548253 41548253 + Missense_Mutation SNP A A G TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr22:41548253A>G c.3041A>G c.(3040-3042)gAg>gGg p.E1014G COAD 22 41548253 41548253 + Missense_Mutation SNP A A G TCGA-CM-5868-01A-01D-1650-10 TCGA-CM-5868-10A-01D-1650-10 g.chr22:41548253A>G c.3041A>G c.(3040-3042)gAg>gGg p.E1014G COAD 22 41553327 41553327 + Missense_Mutation SNP A A G TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr22:41553327A>G c.3416A>G c.(3415-3417)tAc>tGc p.Y1139C COAD 22 41556696 41556696 + Missense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr22:41556696C>A c.3641C>A c.(3640-3642)tCt>tAt p.S1214Y COAD 22 41556708 41556708 + Missense_Mutation SNP A A G TCGA-AA-3877-01A-01W-0995-10 TCGA-AA-3877-10A-01W-0995-10 g.chr22:41556708A>G c.3653A>G c.(3652-3654)gAc>gGc p.D1218G COAD 22 41560055 41560055 + Splice_Site SNP A A T TCGA-D5-5540-01A-01D-1650-10 TCGA-D5-5540-10A-01D-1650-10 g.chr22:41560055A>T c.e22-1 COAD 22 41560059 41560059 + Missense_Mutation SNP T T G TCGA-D5-5540-01A-01D-1650-10 TCGA-D5-5540-10A-01D-1650-10 g.chr22:41560059T>G c.3731T>G c.(3730-3732)tTt>tGt p.F1244C COAD 22 41562627 41562627 + Missense_Mutation SNP G G T TCGA-A6-6141-01A-11D-1771-10 TCGA-A6-6141-10A-01D-1771-10 g.chr22:41562627G>T c.3831G>T c.(3829-3831)aaG>aaT p.K1277N COAD 22 41564589 41564589 + Silent SNP A A T TCGA-AY-6196-01A-11D-1719-10 TCGA-AY-6196-10A-01D-1719-10 g.chr22:41564589A>T c.4011A>T c.(4009-4011)ccA>ccT p.P1337P COAD 22 41564829 41564829 + Missense_Mutation SNP A A G TCGA-AA-A00R-01A-01W-A005-10 TCGA-AA-A00R-10A-01W-A005-10 g.chr22:41564829A>G c.4130A>G c.(4129-4131)cAt>cGt p.H1377R COAD 22 41566479 41566479 + Silent SNP T T C TCGA-CM-6676-01A-11D-1835-10 TCGA-CM-6676-10A-01D-1835-10 g.chr22:41566479T>C c.4356T>C c.(4354-4356)ccT>ccC p.P1452P COAD 22 41568568 41568568 + Silent SNP T T C TCGA-CK-4952-01A-01D-1719-10 TCGA-CK-4952-10A-01D-1719-10 g.chr22:41568568T>C c.4518T>C c.(4516-4518)ggT>ggC p.G1506G COAD 22 41569717 41569717 + Missense_Mutation SNP A A G TCGA-CM-4752-01A-01D-1408-10 TCGA-CM-4752-10A-01D-1408-10 g.chr22:41569717A>G c.4708A>G c.(4708-4710)Aaa>Gaa p.K1570E COAD 22 41569717 41569717 + Missense_Mutation SNP A A G TCGA-DM-A1DA-01A-11D-A152-10 TCGA-DM-A1DA-10A-01D-A152-10 g.chr22:41569717A>G c.4708A>G c.(4708-4710)Aaa>Gaa p.K1570E COAD 22 41569718 41569718 + Missense_Mutation SNP A A G TCGA-G4-6323-01A-11D-1719-10 TCGA-G4-6323-10A-01D-1720-10 g.chr22:41569718A>G c.4709A>G c.(4708-4710)aAa>aGa p.K1570R COAD 22 41569719 41569719 + Silent SNP A A G TCGA-AA-3697-01A-01D-1719-10 TCGA-AA-3697-11A-01D-1719-10 g.chr22:41569719A>G c.4710A>G c.(4708-4710)aaA>aaG p.K1570K COAD 22 41569719 41569719 + Silent SNP A A G TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr22:41569719A>G c.4710A>G c.(4708-4710)aaA>aaG p.K1570K COAD 22 41569719 41569719 + Silent SNP A A G TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr22:41569719A>G c.4710A>G c.(4708-4710)aaA>aaG p.K1570K COAD 22 41572266 41572266 + Missense_Mutation SNP C C A TCGA-AY-6386-01A-21D-1719-10 TCGA-AY-6386-10A-01D-1719-10 g.chr22:41572266C>A c.4795C>A c.(4795-4797)Cgc>Agc p.R1599S COAD 22 41572266 41572266 + Missense_Mutation SNP C C T TCGA-D5-6539-01A-11D-1719-10 TCGA-D5-6539-10A-01D-1719-10 g.chr22:41572266C>T c.4795C>T c.(4795-4797)Cgc>Tgc p.R1599C COAD 22 41572350 41572350 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr22:41572350C>T c.4879C>T c.(4879-4881)Cgg>Tgg p.R1627W COAD 22 41572351 41572351 + Missense_Mutation SNP G G T TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr22:41572351G>T c.4880G>T c.(4879-4881)cGg>cTg p.R1627L COAD 22 41572357 41572357 + Missense_Mutation SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr22:41572357C>T c.4886C>T c.(4885-4887)gCg>gTg p.A1629V COAD 22 41572420 41572420 + Missense_Mutation SNP C C T TCGA-G4-6323-01A-11D-1719-10 TCGA-G4-6323-10A-01D-1720-10 g.chr22:41572420C>T c.4949C>T c.(4948-4950)tCc>tTc p.S1650F COAD 22 41572510 41572510 + Missense_Mutation SNP G G A TCGA-DM-A1D0-01A-11D-A152-10 TCGA-DM-A1D0-10A-01D-A152-10 g.chr22:41572510G>A c.5039G>A c.(5038-5040)cGc>cAc p.R1680H COAD 22 41572908 41572908 + Silent SNP C C T TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr22:41572908C>T c.5193C>T c.(5191-5193)cgC>cgT p.R1731R COAD 22 41573046 41573046 + Silent SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr22:41573046C>T c.5331C>T c.(5329-5331)ggC>ggT p.G1777G COAD 22 41573200 41573200 + Missense_Mutation SNP C C T TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr22:41573200C>T c.5485C>T c.(5485-5487)Cgc>Tgc p.R1829C COAD 22 41573355 41573355 + Silent SNP C C A TCGA-DM-A1DB-01A-11D-A152-10 TCGA-DM-A1DB-10A-01D-A152-10 g.chr22:41573355C>A c.5640C>A c.(5638-5640)ccC>ccA p.P1880P COAD 22 41573563 41573563 + Missense_Mutation SNP A A G TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr22:41573563A>G c.5848A>G c.(5848-5850)Agg>Ggg p.R1950G COAD 22 41573577 41573577 + Silent SNP C C T TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr22:41573577C>T c.5862C>T c.(5860-5862)caC>caT p.H1954H COAD 22 41573590 41573590 + Missense_Mutation SNP A A G TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr22:41573590A>G c.5875A>G c.(5875-5877)Atg>Gtg p.M1959V COAD 22 41574377 41574377 + Missense_Mutation SNP C C T TCGA-AA-3655-01A-02D-1719-10 TCGA-AA-3655-11A-01D-1719-10 g.chr22:41574377C>T c.6662C>T c.(6661-6663)cCa>cTa p.P2221L COAD 22 41574487 41574487 + Nonsense_Mutation SNP C C T TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr22:41574487C>T c.6772C>T c.(6772-6774)Cag>Tag p.Q2258* COAD 22 41574534 41574534 + Silent SNP T T G TCGA-AA-3869-01A-01W-0995-10 TCGA-AA-3869-10A-01W-0995-10 g.chr22:41574534T>G c.6819T>G c.(6817-6819)gtT>gtG p.V2273V COAD 22 41574684 41574684 + Silent SNP C C T TCGA-D5-5538-01A-01D-1650-10 TCGA-D5-5538-10A-02D-1650-10 g.chr22:41574684C>T c.6969C>T c.(6967-6969)ccC>ccT p.P2323P COADREAD 22 41513284 41513284 + Missense_Mutation SNP A A G TCGA-A6-5659-01A-01D-1650-10 TCGA-A6-5659-11A-01D-1650-10 g.chr22:41513284A>G c.188A>G c.(187-189)cAg>cGg p.Q63R COADREAD 22 41513293 41513293 + Missense_Mutation SNP C C T TCGA-AA-3554-01A-01W-0833-10 TCGA-AA-3554-10A-01W-0833-10 g.chr22:41513293C>T c.197C>T c.(196-198)aCa>aTa p.T66I COADREAD 22 41513347 41513347 + Missense_Mutation SNP T T C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr22:41513347T>C c.251T>C c.(250-252)tTg>tCg p.L84S COADREAD 22 41513353 41513353 + Missense_Mutation SNP G G A TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr22:41513353G>A c.257G>A c.(256-258)cGa>cAa p.R86Q COADREAD 22 41513353 41513353 + Missense_Mutation SNP G G A TCGA-CM-4752-01A-01D-1408-10 TCGA-CM-4752-10A-01D-1408-10 g.chr22:41513353G>A c.257G>A c.(256-258)cGa>cAa p.R86Q COADREAD 22 41513474 41513474 + Missense_Mutation SNP G G A TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr22:41513474G>A c.378G>A c.(376-378)atG>atA p.M126I COADREAD 22 41513540 41513540 + Silent SNP G G A TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr22:41513540G>A c.444G>A c.(442-444)acG>acA p.T148T COADREAD 22 41513646 41513646 + Nonsense_Mutation SNP C C T TCGA-DC-6682-01A-11D-1826-10 TCGA-DC-6682-10A-01D-1826-10 g.chr22:41513646C>T c.550C>T c.(550-552)Caa>Taa p.Q184* COADREAD 22 41513675 41513675 + Silent SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr22:41513675C>T c.579C>T c.(577-579)aaC>aaT p.N193N COADREAD 22 41523526 41523526 + Silent SNP C C T TCGA-DY-A1DD-01A-21D-A152-10 TCGA-DY-A1DD-10A-01D-A152-10 g.chr22:41523526C>T c.942C>T c.(940-942)ggC>ggT p.G314G COADREAD 22 41523729 41523729 + Missense_Mutation SNP G G A TCGA-AA-A01G-01A-01W-A005-10 TCGA-AA-A01G-10A-01W-A005-10 g.chr22:41523729G>A c.1145G>A c.(1144-1146)tGc>tAc p.C382Y COADREAD 22 41525931 41525931 + Silent SNP C C T TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr22:41525931C>T c.1206C>T c.(1204-1206)caC>caT p.H402H COADREAD 22 41527630 41527630 + Silent SNP C C T TCGA-AY-5543-01A-01D-1650-10 TCGA-AY-5543-10A-01D-1650-10 g.chr22:41527630C>T c.1521C>T c.(1519-1521)agC>agT p.S507S COADREAD 22 41527630 41527630 + Silent SNP C C T TCGA-CM-6166-01A-11D-1650-10 TCGA-CM-6166-10A-01D-1650-10 g.chr22:41527630C>T c.1521C>T c.(1519-1521)agC>agT p.S507S COADREAD 22 41531883 41531883 + Missense_Mutation SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr22:41531883T>G c.1595T>G c.(1594-1596)aTg>aGg p.M532R COADREAD 22 41533736 41533736 + Missense_Mutation SNP C C T TCGA-AA-3555-01A-01W-0831-10 TCGA-AA-3555-10A-01W-0831-10 g.chr22:41533736C>T c.1702C>T c.(1702-1704)Cgg>Tgg p.R568W COADREAD 22 41533773 41533773 + Missense_Mutation SNP G G A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr22:41533773G>A c.1739G>A c.(1738-1740)cGa>cAa p.R580Q COADREAD 22 41533773 41533773 + Missense_Mutation SNP G G A TCGA-D5-6920-01A-11D-1924-10 TCGA-D5-6920-10A-01D-1924-10 g.chr22:41533773G>A c.1739G>A c.(1738-1740)cGa>cAa p.R580Q COADREAD 22 41533793 41533793 + Splice_Site SNP C C T TCGA-D5-6931-01A-11D-1924-10 TCGA-D5-6931-10A-01D-1924-10 g.chr22:41533793C>T c.1759C>T c.(1759-1761)Ctc>Ttc p.L587F COADREAD 22 41536153 41536153 + Silent SNP C C T TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr22:41536153C>T c.1770C>T c.(1768-1770)gcC>gcT p.A590A COADREAD 22 41536167 41536167 + Missense_Mutation SNP C C T TCGA-CA-5796-01A-01D-1650-10 TCGA-CA-5796-10A-01D-1650-10 g.chr22:41536167C>T c.1784C>T c.(1783-1785)cCg>cTg p.P595L COADREAD 22 41536193 41536193 + Missense_Mutation SNP C C G TCGA-AA-3527-01A-01W-0831-10 TCGA-AA-3527-10A-01W-0831-10 g.chr22:41536193C>G c.1810C>G c.(1810-1812)Cgg>Ggg p.R604G COADREAD 22 41545847 41545847 + Missense_Mutation SNP A A G TCGA-AA-3662-01A-01D-1719-10 TCGA-AA-3662-11A-01D-1719-10 g.chr22:41545847A>G c.2462A>G c.(2461-2463)cAg>cGg p.Q821R COADREAD 22 41545897 41545897 + Missense_Mutation SNP C C T TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr22:41545897C>T c.2512C>T c.(2512-2514)Cgt>Tgt p.R838C COADREAD 22 41545903 41545903 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr22:41545903C>A c.2518C>A c.(2518-2520)Ccc>Acc p.P840T COADREAD 22 41547864 41547864 + Nonsense_Mutation SNP G G T TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr22:41547864G>T c.2845G>T c.(2845-2847)Gga>Tga p.G949* COADREAD 22 41548250 41548250 + Missense_Mutation SNP A A G TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr22:41548250A>G c.3038A>G c.(3037-3039)gAa>gGa p.E1013G COADREAD 22 41548251 41548251 + Silent SNP A A G TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr22:41548251A>G c.3039A>G c.(3037-3039)gaA>gaG p.E1013E COADREAD 22 41548251 41548251 + Silent SNP A A G TCGA-D5-6533-01A-11D-1719-10 TCGA-D5-6533-10A-01D-1719-10 g.chr22:41548251A>G c.3039A>G c.(3037-3039)gaA>gaG p.E1013E COADREAD 22 41548251 41548251 + Silent SNP A A G TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr22:41548251A>G c.3039A>G c.(3037-3039)gaA>gaG p.E1013E COADREAD 22 41548253 41548253 + Missense_Mutation SNP A A G TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr22:41548253A>G c.3041A>G c.(3040-3042)gAg>gGg p.E1014G COADREAD 22 41548253 41548253 + Missense_Mutation SNP A A G TCGA-CM-5868-01A-01D-1650-10 TCGA-CM-5868-10A-01D-1650-10 g.chr22:41548253A>G c.3041A>G c.(3040-3042)gAg>gGg p.E1014G COADREAD 22 41548253 41548253 + Missense_Mutation SNP A A G TCGA-DC-6682-01A-11D-1826-10 TCGA-DC-6682-10A-01D-1826-10 g.chr22:41548253A>G c.3041A>G c.(3040-3042)gAg>gGg p.E1014G COADREAD 22 41553327 41553327 + Missense_Mutation SNP A A G TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr22:41553327A>G c.3416A>G c.(3415-3417)tAc>tGc p.Y1139C COADREAD 22 41556696 41556696 + Missense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr22:41556696C>A c.3641C>A c.(3640-3642)tCt>tAt p.S1214Y COADREAD 22 41556708 41556708 + Missense_Mutation SNP A A G TCGA-AA-3877-01A-01W-0995-10 TCGA-AA-3877-10A-01W-0995-10 g.chr22:41556708A>G c.3653A>G c.(3652-3654)gAc>gGc p.D1218G COADREAD 22 41560055 41560055 + Splice_Site SNP A A T TCGA-D5-5540-01A-01D-1650-10 TCGA-D5-5540-10A-01D-1650-10 g.chr22:41560055A>T c.e22-1 COADREAD 22 41560059 41560059 + Missense_Mutation SNP T T G TCGA-D5-5540-01A-01D-1650-10 TCGA-D5-5540-10A-01D-1650-10 g.chr22:41560059T>G c.3731T>G c.(3730-3732)tTt>tGt p.F1244C COADREAD 22 41562627 41562627 + Missense_Mutation SNP G G T TCGA-A6-6141-01A-11D-1771-10 TCGA-A6-6141-10A-01D-1771-10 g.chr22:41562627G>T c.3831G>T c.(3829-3831)aaG>aaT p.K1277N COADREAD 22 41564512 41564512 + Nonsense_Mutation SNP C C T TCGA-G5-6641-01A-11D-1826-10 TCGA-G5-6641-10A-01D-1826-10 g.chr22:41564512C>T c.3934C>T c.(3934-3936)Cga>Tga p.R1312* COADREAD 22 41564589 41564589 + Silent SNP A A T TCGA-AY-6196-01A-11D-1719-10 TCGA-AY-6196-10A-01D-1719-10 g.chr22:41564589A>T c.4011A>T c.(4009-4011)ccA>ccT p.P1337P COADREAD 22 41564829 41564829 + Missense_Mutation SNP A A G TCGA-AA-A00R-01A-01W-A005-10 TCGA-AA-A00R-10A-01W-A005-10 g.chr22:41564829A>G c.4130A>G c.(4129-4131)cAt>cGt p.H1377R COADREAD 22 41566479 41566479 + Silent SNP T T C TCGA-CM-6676-01A-11D-1835-10 TCGA-CM-6676-10A-01D-1835-10 g.chr22:41566479T>C c.4356T>C c.(4354-4356)ccT>ccC p.P1452P COADREAD 22 41568568 41568568 + Silent SNP T T C TCGA-CK-4952-01A-01D-1719-10 TCGA-CK-4952-10A-01D-1719-10 g.chr22:41568568T>C c.4518T>C c.(4516-4518)ggT>ggC p.G1506G COADREAD 22 41569717 41569717 + Missense_Mutation SNP A A G TCGA-CI-6619-01B-11D-1826-10 TCGA-CI-6619-10A-01D-1826-10 g.chr22:41569717A>G c.4708A>G c.(4708-4710)Aaa>Gaa p.K1570E COADREAD 22 41569717 41569717 + Missense_Mutation SNP A A G TCGA-CM-4752-01A-01D-1408-10 TCGA-CM-4752-10A-01D-1408-10 g.chr22:41569717A>G c.4708A>G c.(4708-4710)Aaa>Gaa p.K1570E COADREAD 22 41569717 41569717 + Missense_Mutation SNP A A G TCGA-DM-A1DA-01A-11D-A152-10 TCGA-DM-A1DA-10A-01D-A152-10 g.chr22:41569717A>G c.4708A>G c.(4708-4710)Aaa>Gaa p.K1570E COADREAD 22 41569718 41569718 + Missense_Mutation SNP A A G TCGA-AG-3732-01A-11D-1657-10 TCGA-AG-3732-11A-01D-1657-10 g.chr22:41569718A>G c.4709A>G c.(4708-4710)aAa>aGa p.K1570R COADREAD 22 41569718 41569718 + Missense_Mutation SNP A A G TCGA-G4-6323-01A-11D-1719-10 TCGA-G4-6323-10A-01D-1720-10 g.chr22:41569718A>G c.4709A>G c.(4708-4710)aAa>aGa p.K1570R COADREAD 22 41569719 41569719 + Silent SNP A A G TCGA-AA-3697-01A-01D-1719-10 TCGA-AA-3697-11A-01D-1719-10 g.chr22:41569719A>G c.4710A>G c.(4708-4710)aaA>aaG p.K1570K COADREAD 22 41569719 41569719 + Silent SNP A A G TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr22:41569719A>G c.4710A>G c.(4708-4710)aaA>aaG p.K1570K COADREAD 22 41569719 41569719 + Silent SNP A A G TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr22:41569719A>G c.4710A>G c.(4708-4710)aaA>aaG p.K1570K COADREAD 22 41572266 41572266 + Missense_Mutation SNP C C A TCGA-AY-6386-01A-21D-1719-10 TCGA-AY-6386-10A-01D-1719-10 g.chr22:41572266C>A c.4795C>A c.(4795-4797)Cgc>Agc p.R1599S COADREAD 22 41572266 41572266 + Missense_Mutation SNP C C T TCGA-D5-6539-01A-11D-1719-10 TCGA-D5-6539-10A-01D-1719-10 g.chr22:41572266C>T c.4795C>T c.(4795-4797)Cgc>Tgc p.R1599C COADREAD 22 41572266 41572266 + Missense_Mutation SNP C C T TCGA-G5-6235-01A-11D-1733-10 TCGA-G5-6235-10A-01D-1733-10 g.chr22:41572266C>T c.4795C>T c.(4795-4797)Cgc>Tgc p.R1599C COADREAD 22 41572350 41572350 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr22:41572350C>T c.4879C>T c.(4879-4881)Cgg>Tgg p.R1627W COADREAD 22 41572350 41572350 + Missense_Mutation SNP C C T TCGA-EI-6510-01A-11D-1733-10 TCGA-EI-6510-10A-01D-1733-10 g.chr22:41572350C>T c.4879C>T c.(4879-4881)Cgg>Tgg p.R1627W COADREAD 22 41572351 41572351 + Missense_Mutation SNP G G T TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr22:41572351G>T c.4880G>T c.(4879-4881)cGg>cTg p.R1627L COADREAD 22 41572357 41572357 + Missense_Mutation SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr22:41572357C>T c.4886C>T c.(4885-4887)gCg>gTg p.A1629V COADREAD 22 41572420 41572420 + Missense_Mutation SNP C C T TCGA-G4-6323-01A-11D-1719-10 TCGA-G4-6323-10A-01D-1720-10 g.chr22:41572420C>T c.4949C>T c.(4948-4950)tCc>tTc p.S1650F COADREAD 22 41572510 41572510 + Missense_Mutation SNP G G A TCGA-DM-A1D0-01A-11D-A152-10 TCGA-DM-A1D0-10A-01D-A152-10 g.chr22:41572510G>A c.5039G>A c.(5038-5040)cGc>cAc p.R1680H COADREAD 22 41572510 41572510 + Missense_Mutation SNP G G A TCGA-F5-6813-01A-11D-1826-10 TCGA-F5-6813-10A-01D-1826-10 g.chr22:41572510G>A c.5039G>A c.(5038-5040)cGc>cAc p.R1680H COADREAD 22 41572908 41572908 + Silent SNP C C T TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr22:41572908C>T c.5193C>T c.(5191-5193)cgC>cgT p.R1731R COADREAD 22 41573046 41573046 + Silent SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr22:41573046C>T c.5331C>T c.(5329-5331)ggC>ggT p.G1777G COADREAD 22 41573200 41573200 + Missense_Mutation SNP C C T TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr22:41573200C>T c.5485C>T c.(5485-5487)Cgc>Tgc p.R1829C COADREAD 22 41573355 41573355 + Silent SNP C C A TCGA-DM-A1DB-01A-11D-A152-10 TCGA-DM-A1DB-10A-01D-A152-10 g.chr22:41573355C>A c.5640C>A c.(5638-5640)ccC>ccA p.P1880P COADREAD 22 41573425 41573425 + Nonsense_Mutation SNP C C T TCGA-AF-2687-01A-02D-1733-10 TCGA-AF-2687-10A-01D-1733-10 g.chr22:41573425C>T c.5710C>T c.(5710-5712)Cag>Tag p.Q1904* COADREAD 22 41573563 41573563 + Missense_Mutation SNP A A G TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr22:41573563A>G c.5848A>G c.(5848-5850)Agg>Ggg p.R1950G COADREAD 22 41573577 41573577 + Silent SNP C C T TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr22:41573577C>T c.5862C>T c.(5860-5862)caC>caT p.H1954H COADREAD 22 41573590 41573590 + Missense_Mutation SNP A A G TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr22:41573590A>G c.5875A>G c.(5875-5877)Atg>Gtg p.M1959V COADREAD 22 41574238 41574238 + Missense_Mutation SNP A A G TCGA-G5-6235-01A-11D-1733-10 TCGA-G5-6235-10A-01D-1733-10 g.chr22:41574238A>G c.6523A>G c.(6523-6525)Atg>Gtg p.M2175V COADREAD 22 41574377 41574377 + Missense_Mutation SNP C C T TCGA-AA-3655-01A-02D-1719-10 TCGA-AA-3655-11A-01D-1719-10 g.chr22:41574377C>T c.6662C>T c.(6661-6663)cCa>cTa p.P2221L COADREAD 22 41574377 41574377 + Missense_Mutation SNP C C T TCGA-G5-6235-01A-11D-1733-10 TCGA-G5-6235-10A-01D-1733-10 g.chr22:41574377C>T c.6662C>T c.(6661-6663)cCa>cTa p.P2221L COADREAD 22 41574487 41574487 + Nonsense_Mutation SNP C C T TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr22:41574487C>T c.6772C>T c.(6772-6774)Cag>Tag p.Q2258* COADREAD 22 41574534 41574534 + Silent SNP T T G TCGA-AA-3869-01A-01W-0995-10 TCGA-AA-3869-10A-01W-0995-10 g.chr22:41574534T>G c.6819T>G c.(6817-6819)gtT>gtG p.V2273V COADREAD 22 41574679 41574679 + Frame_Shift_Del DEL C C - TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr22:41574679delC c.6964delC c.(6964-6966)cccfs p.P2323fs COADREAD 22 41574684 41574684 + Silent SNP C C T TCGA-D5-5538-01A-01D-1650-10 TCGA-D5-5538-10A-02D-1650-10 g.chr22:41574684C>T c.6969C>T c.(6967-6969)ccC>ccT p.P2323P COADREAD 22 41574836 41574836 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr22:41574836C>A c.7121C>A c.(7120-7122)tCt>tAt p.S2374Y DLBC 22 41542753 41542753 + Silent SNP A A G TCGA-G8-6326-01A-11D-2210-10 TCGA-G8-6326-10A-01D-2210-10 g.chr22:41542753A>G c.2064A>G c.(2062-2064)ctA>ctG p.L688L DLBC 22 41546158 41546158 + Missense_Mutation SNP C C A TCGA-GR-7353-01A-11D-2210-10 TCGA-GR-7353-10A-01D-2210-10 g.chr22:41546158C>A c.2773C>A c.(2773-2775)Cct>Act p.P925T DLBC 22 41572795 41572795 + Missense_Mutation SNP A A G TCGA-GR-A4D6-01A-11D-A31X-10 TCGA-GR-A4D6-10A-01D-A31X-10 g.chr22:41572795A>G c.5080A>G c.(5080-5082)Acc>Gcc p.T1694A DLBC 22 41574383 41574383 + Missense_Mutation SNP A A C TCGA-G8-6914-01A-11D-2210-10 TCGA-G8-6914-14A-01D-2210-10 g.chr22:41574383A>C c.6668A>C c.(6667-6669)cAg>cCg p.Q2223P ESCA 22 41513396 41513396 + Silent SNP A A G TCGA-L5-A8NM-01A-11D-A37C-09 TCGA-L5-A8NM-11A-12D-A37F-09 g.chr22:41513396A>G c.300A>G c.(298-300)ccA>ccG p.P100P ESCA 22 41536233 41536233 + Missense_Mutation SNP G G T TCGA-R6-A6L4-01A-11D-A31U-09 TCGA-R6-A6L4-10A-01D-A31U-09 g.chr22:41536233G>T c.1850G>T c.(1849-1851)gGg>gTg p.G617V ESCA 22 41547895 41547895 + Missense_Mutation SNP G G A TCGA-2H-A9GF-01A-11D-A37C-09 TCGA-2H-A9GF-11A-11D-A37F-09 g.chr22:41547895G>A c.2876G>A c.(2875-2877)aGc>aAc p.S959N ESCA 22 41553298 41553298 + Missense_Mutation SNP G G T TCGA-L5-A4OH-01A-11D-A27G-09 TCGA-L5-A4OH-11A-11D-A27G-09 g.chr22:41553298G>T c.3387G>T c.(3385-3387)tgG>tgT p.W1129C ESCA 22 41558785 41558785 + Splice_Site SNP T T A TCGA-LN-A9FO-01A-11D-A387-09 TCGA-LN-A9FO-10A-01D-A38A-09 g.chr22:41558785T>A c.e21+2 ESCA 22 41564862 41564862 + Missense_Mutation SNP C C A TCGA-JY-A6FD-01A-11D-A33E-09 TCGA-JY-A6FD-10A-01D-A33H-09 g.chr22:41564862C>A c.4163C>A c.(4162-4164)cCc>cAc p.P1388H ESCA 22 41565533 41565533 + Missense_Mutation SNP G G T TCGA-LN-A49P-01A-11D-A247-09 TCGA-LN-A49P-10A-01D-A247-09 g.chr22:41565533G>T c.4199G>T c.(4198-4200)aGt>aTt p.S1400I ESCA 22 41565565 41565565 + Missense_Mutation SNP A A G TCGA-R6-A6Y0-01B-11D-A33E-09 TCGA-R6-A6Y0-10A-01D-A33H-09 g.chr22:41565565A>G c.4231A>G c.(4231-4233)Act>Gct p.T1411A ESCA 22 41565574 41565574 + Missense_Mutation SNP T T G TCGA-IG-A5B8-01A-11D-A28B-09 TCGA-IG-A5B8-10A-01D-A28E-09 g.chr22:41565574T>G c.4240T>G c.(4240-4242)Tat>Gat p.Y1414D ESCA 22 41568668 41568668 + Splice_Site SNP G G A TCGA-LN-A49V-01A-11D-A247-09 TCGA-LN-A49V-10A-01D-A247-09 g.chr22:41568668G>A c.e28+1 ESCA 22 41572509 41572509 + Missense_Mutation SNP C C T TCGA-ZR-A9CJ-01B-11D-A387-09 TCGA-ZR-A9CJ-10A-01D-A38A-09 g.chr22:41572509C>T c.5038C>T c.(5038-5040)Cgc>Tgc p.R1680C ESCA 22 41574330 41574330 + Missense_Mutation SNP G G T TCGA-IG-A6QS-01A-12D-A33E-09 TCGA-IG-A6QS-10B-01D-A33H-09 g.chr22:41574330G>T c.6615G>T c.(6613-6615)atG>atT p.M2205I ESCA 22 41574679 41574679 + Frame_Shift_Del DEL C C - TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr22:41574679delC c.6964delC c.(6964-6966)cccfs p.P2323fs GBM 22 41556657 41556657 + Missense_Mutation SNP G G A TCGA-26-6173-01A-11D-1845-08 TCGA-26-6173-10A-01D-1845-08 g.chr22:41556657G>A c.3602G>A c.(3601-3603)tGt>tAt p.C1201Y GBM 22 41564740 41564740 + Silent SNP A A G TCGA-02-2483-01A-01D-1494-08 TCGA-02-2483-10A-01D-1494-08 g.chr22:41564740A>G c.4041A>G c.(4039-4041)ggA>ggG p.G1347G GBM 22 41564810 41564810 + Silent SNP C C T TCGA-06-0214-01A-02D-1491-08 TCGA-06-0214-10A-01D-1491-08 g.chr22:41564810C>T c.4111C>T c.(4111-4113)Ctg>Ttg p.L1371L GBMLGG 22 41513608 41513608 + Missense_Mutation SNP C C T TCGA-P5-A77X-01A-11D-A32B-08 TCGA-P5-A77X-10A-01D-A329-08 g.chr22:41513608C>T c.512C>T c.(511-513)gCg>gTg p.A171V GBMLGG 22 41523588 41523588 + Missense_Mutation SNP G G A TCGA-DU-A7TA-01A-11D-A33T-08 TCGA-DU-A7TA-10A-01D-A33W-08 g.chr22:41523588G>A c.1004G>A c.(1003-1005)cGc>cAc p.R335H GBMLGG 22 41556657 41556657 + Missense_Mutation SNP G G A TCGA-26-6173-01A-11D-1845-08 TCGA-26-6173-10A-01D-1845-08 g.chr22:41556657G>A c.3602G>A c.(3601-3603)tGt>tAt p.C1201Y GBMLGG 22 41564740 41564740 + Silent SNP A A G TCGA-02-2483-01A-01D-1494-08 TCGA-02-2483-10A-01D-1494-08 g.chr22:41564740A>G c.4041A>G c.(4039-4041)ggA>ggG p.G1347G GBMLGG 22 41564810 41564810 + Silent SNP C C T TCGA-06-0214-01A-02D-1491-08 TCGA-06-0214-10A-01D-1491-08 g.chr22:41564810C>T c.4111C>T c.(4111-4113)Ctg>Ttg p.L1371L GBMLGG 22 41566461 41566461 + Silent SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr22:41566461T>C c.4338T>C c.(4336-4338)taT>taC p.Y1446Y GBMLGG 22 41566476 41566476 + Silent SNP T T C TCGA-DB-A64V-01A-11D-A29Q-08 TCGA-DB-A64V-10A-01D-A29Q-08 g.chr22:41566476T>C c.4353T>C c.(4351-4353)caT>caC p.H1451H GBMLGG 22 41574489 41574489 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr22:41574489G>T c.6774G>T c.(6772-6774)caG>caT p.Q2258H GBMLGG 22 41574637 41574637 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr22:41574637C>T c.6922C>T c.(6922-6924)Cgc>Tgc p.R2308C GBMLGG 22 41574836 41574836 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr22:41574836C>A c.7121C>A c.(7120-7122)tCt>tAt p.S2374Y HNSC 22 41489079 41489079 + Nonsense_Mutation SNP C C A TCGA-CV-7178-01A-21D-2012-08 TCGA-CV-7178-10A-01D-2013-08 g.chr22:41489079C>A c.71C>A c.(70-72)tCg>tAg p.S24* HNSC 22 41513481 41513481 + Missense_Mutation SNP G G T TCGA-MZ-A7D7-01A-21D-A34J-08 TCGA-MZ-A7D7-10A-01D-A34M-08 g.chr22:41513481G>T c.385G>T c.(385-387)Gca>Tca p.A129S HNSC 22 41513521 41513521 + Missense_Mutation SNP G G T TCGA-CV-6943-01A-11D-1912-08 TCGA-CV-6943-10A-01D-1912-08 g.chr22:41513521G>T c.425G>T c.(424-426)gGa>gTa p.G142V HNSC 22 41513816 41513816 + Missense_Mutation SNP G G T TCGA-HD-A6HZ-01A-12D-A31L-08 TCGA-HD-A6HZ-10A-01D-A31J-08 g.chr22:41513816G>T c.720G>T c.(718-720)caG>caT p.Q240H HNSC 22 41525914 41525914 + Nonsense_Mutation SNP C C T TCGA-QK-A6IG-01A-11D-A31L-08 TCGA-QK-A6IG-10A-01D-A31J-08 g.chr22:41525914C>T c.1189C>T c.(1189-1191)Cga>Tga p.R397* HNSC 22 41531855 41531855 + Nonsense_Mutation SNP C C T TCGA-CR-6487-01A-11D-1870-08 TCGA-CR-6487-10A-01D-1870-08 g.chr22:41531855C>T c.1567C>T c.(1567-1569)Caa>Taa p.Q523* HNSC 22 41545804 41545804 + Missense_Mutation SNP A A G TCGA-BA-4075-01A-01D-1434-08 TCGA-BA-4075-10A-01D-1434-08 g.chr22:41545804A>G c.2419A>G c.(2419-2421)Ata>Gta p.I807V HNSC 22 41547861 41547861 + Missense_Mutation SNP G G A TCGA-CV-6938-01A-11D-1912-08 TCGA-CV-6938-10A-01D-1912-08 g.chr22:41547861G>A c.2842G>A c.(2842-2844)Gaa>Aaa p.E948K HNSC 22 41547912 41547912 + Nonsense_Mutation SNP C C T TCGA-CQ-5327-01A-01D-1683-08 TCGA-CQ-5327-10A-01D-1683-08 g.chr22:41547912C>T c.2893C>T c.(2893-2895)Cag>Tag p.Q965* HNSC 22 41547937 41547937 + Missense_Mutation SNP C C T TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr22:41547937C>T c.2918C>T c.(2917-2919)tCc>tTc p.S973F HNSC 22 41553243 41553243 + Missense_Mutation SNP A A G TCGA-BB-A6UO-01A-12D-A34J-08 TCGA-BB-A6UO-10A-01D-A34M-08 g.chr22:41553243A>G c.3332A>G c.(3331-3333)tAt>tGt p.Y1111C HNSC 22 41553402 41553402 + Missense_Mutation SNP G G A TCGA-BA-5559-01A-01D-1512-08 TCGA-BA-5559-10A-01D-1512-08 g.chr22:41553402G>A c.3491G>A c.(3490-3492)tGt>tAt p.C1164Y HNSC 22 41553402 41553402 + Missense_Mutation SNP G G A TCGA-CQ-5326-01A-01D-1870-08 TCGA-CQ-5326-10A-01D-1870-08 g.chr22:41553402G>A c.3491G>A c.(3490-3492)tGt>tAt p.C1164Y HNSC 22 41556666 41556666 + Missense_Mutation SNP G G A TCGA-CQ-5331-01A-02D-1870-08 TCGA-CQ-5331-10A-01D-1870-08 g.chr22:41556666G>A c.3611G>A c.(3610-3612)tGt>tAt p.C1204Y HNSC 22 41556727 41556727 + Splice_Site SNP G G A TCGA-CN-A642-01A-12D-A30E-08 TCGA-CN-A642-10A-01D-A30H-08 g.chr22:41556727G>A c.e20+1 HNSC 22 41556727 41556727 + Splice_Site SNP G G T TCGA-CN-A63W-01A-11D-A30E-08 TCGA-CN-A63W-10A-01D-A30H-08 g.chr22:41556727G>T c.e20+1 HNSC 22 41564727 41564727 + Missense_Mutation SNP T T G TCGA-CX-7219-01A-11D-2012-08 TCGA-CX-7219-10A-01D-2013-08 g.chr22:41564727T>G c.4028T>G c.(4027-4029)tTt>tGt p.F1343C HNSC 22 41564866 41564866 + Missense_Mutation SNP C C G TCGA-H7-7774-01A-21D-2078-08 TCGA-H7-7774-10A-01D-2078-08 g.chr22:41564866C>G c.4167C>G c.(4165-4167)aaC>aaG p.N1389K HNSC 22 41565529 41565529 + Missense_Mutation SNP G G A TCGA-BB-A6UM-01A-12D-A34J-08 TCGA-BB-A6UM-10A-01D-A34M-08 g.chr22:41565529G>A c.4195G>A c.(4195-4197)Gat>Aat p.D1399N HNSC 22 41565529 41565529 + Missense_Mutation SNP G G A TCGA-CR-6470-01A-11D-1870-08 TCGA-CR-6470-10A-01D-1870-08 g.chr22:41565529G>A c.4195G>A c.(4195-4197)Gat>Aat p.D1399N HNSC 22 41565529 41565529 + Missense_Mutation SNP G G A TCGA-CV-7100-01A-11D-2012-08 TCGA-CV-7100-10A-01D-2013-08 g.chr22:41565529G>A c.4195G>A c.(4195-4197)Gat>Aat p.D1399N HNSC 22 41565529 41565529 + Missense_Mutation SNP G G A TCGA-CV-7427-01A-11D-2078-08 TCGA-CV-7427-10A-01D-2078-08 g.chr22:41565529G>A c.4195G>A c.(4195-4197)Gat>Aat p.D1399N HNSC 22 41565529 41565529 + Missense_Mutation SNP G G A TCGA-DQ-7593-01A-11D-2229-08 TCGA-DQ-7593-10D-01D-2229-08 g.chr22:41565529G>A c.4195G>A c.(4195-4197)Gat>Aat p.D1399N HNSC 22 41565564 41565564 + Missense_Mutation SNP G G T TCGA-BA-A6DA-01A-31D-A31L-08 TCGA-BA-A6DA-10A-01D-A31J-08 g.chr22:41565564G>T c.4230G>T c.(4228-4230)agG>agT p.R1410S HNSC 22 41566460 41566460 + Missense_Mutation SNP A A G TCGA-CR-6471-01A-11D-1870-08 TCGA-CR-6471-10A-01D-1870-08 g.chr22:41566460A>G c.4337A>G c.(4336-4338)tAt>tGt p.Y1446C HNSC 22 41566476 41566478 + In_Frame_Del DEL TCC TCC - TCGA-BB-7870-01A-11D-2229-08 TCGA-BB-7870-10A-01D-2229-08 g.chr22:41566476_41566478delTCC c.4353_4355delTCC c.(4351-4356)catcct>cat p.P1453del HNSC 22 41566478 41566478 + Missense_Mutation SNP C C T TCGA-P3-A6T4-01A-11D-A34J-08 TCGA-P3-A6T4-10A-01D-A34M-08 g.chr22:41566478C>T c.4355C>T c.(4354-4356)cCt>cTt p.P1452L HNSC 22 41566521 41566521 + Missense_Mutation SNP G G C TCGA-CV-5434-01A-01D-1683-08 TCGA-CV-5434-10A-01D-1870-08 g.chr22:41566521G>C c.4398G>C c.(4396-4398)tgG>tgC p.W1466C HNSC 22 41566523 41566523 + Missense_Mutation SNP A A C TCGA-F7-A623-01A-11D-A28R-08 TCGA-F7-A623-10A-01D-A28U-08 g.chr22:41566523A>C c.4400A>C c.(4399-4401)tAc>tCc p.Y1467S HNSC 22 41568555 41568555 + Missense_Mutation SNP C C T TCGA-CV-A468-01A-11D-A25Y-08 TCGA-CV-A468-10A-01D-A25Y-08 g.chr22:41568555C>T c.4505C>T c.(4504-4506)cCt>cTt p.P1502L HNSC 22 41568590 41568590 + Missense_Mutation SNP G G A TCGA-CN-A6V6-01A-12D-A34J-08 TCGA-CN-A6V6-10A-01D-A34M-08 g.chr22:41568590G>A c.4540G>A c.(4540-4542)Gaa>Aaa p.E1514K HNSC 22 41568590 41568590 + Missense_Mutation SNP G G A TCGA-CR-7394-01A-11D-2012-08 TCGA-CR-7394-10A-01D-2013-08 g.chr22:41568590G>A c.4540G>A c.(4540-4542)Gaa>Aaa p.E1514K HNSC 22 41569760 41569760 + Missense_Mutation SNP T T C TCGA-CV-A6JD-01A-11D-A31L-08 TCGA-CV-A6JD-10A-01D-A31J-08 g.chr22:41569760T>C c.4751T>C c.(4750-4752)cTa>cCa p.L1584P HNSC 22 41572250 41572250 + Splice_Site SNP G G A TCGA-CR-7395-01A-11D-2012-08 TCGA-CR-7395-10A-01D-2013-08 g.chr22:41572250G>A c.e30-1 HNSC 22 41572777 41572777 + Splice_Site SNP G G C TCGA-P3-A5Q5-01A-11D-A28R-08 TCGA-P3-A5Q5-10A-01D-A28U-08 g.chr22:41572777G>C c.5062G>C c.(5062-5064)Gat>Cat p.D1688H HNSC 22 41573028 41573028 + Nonsense_Mutation SNP C C A TCGA-CV-7095-01A-21D-2012-08 TCGA-CV-7095-10A-01D-2013-08 g.chr22:41573028C>A c.5313C>A c.(5311-5313)tgC>tgA p.C1771* HNSC 22 41574519 41574519 + Silent SNP G G A TCGA-CR-7394-01A-11D-2012-08 TCGA-CR-7394-10A-01D-2013-08 g.chr22:41574519G>A c.6804G>A c.(6802-6804)caG>caA p.Q2268Q HNSC 22 41574850 41574850 + Missense_Mutation SNP A A C TCGA-BA-4076-01A-01D-1434-08 TCGA-BA-4076-10A-01D-1434-08 g.chr22:41574850A>C c.7135A>C c.(7135-7137)Aat>Cat p.N2379H HNSC 22 41574914 41574914 + Nonsense_Mutation SNP C C G TCGA-CV-A6K2-01A-11D-A31L-08 TCGA-CV-A6K2-10A-01D-A31J-08 g.chr22:41574914C>G c.7199C>G c.(7198-7200)tCa>tGa p.S2400* KIPAN 22 41513594 41513594 + Missense_Mutation SNP C C A TCGA-B0-5713-01A-11D-1669-08 TCGA-B0-5713-11A-01D-1669-08 g.chr22:41513594C>A c.498C>A c.(496-498)aaC>aaA p.N166K KIPAN 22 41527606 41527606 + Silent SNP T T C TCGA-5P-A9K3-01A-11D-A42J-10 TCGA-5P-A9K3-10A-01D-A42M-10 g.chr22:41527606T>C c.1497T>C c.(1495-1497)tcT>tcC p.S499S KIPAN 22 41536219 41536219 + Silent SNP T T C TCGA-AK-3428-01A-02D-1361-10 TCGA-AK-3428-10A-01D-1361-10 g.chr22:41536219T>C c.1836T>C c.(1834-1836)gcT>gcC p.A612A KIPAN 22 41542756 41542756 + Silent SNP T T C TCGA-UZ-A9PK-01A-11D-A382-10 TCGA-UZ-A9PK-10A-01D-A385-10 g.chr22:41542756T>C c.2067T>C c.(2065-2067)ccT>ccC p.P689P KIPAN 22 41545134 41545134 + Frame_Shift_Del DEL A A - TCGA-Y8-A898-01A-11D-A34Z-10 TCGA-Y8-A898-10A-01D-A34Z-10 g.chr22:41545134delA c.2334delA c.(2332-2334)acafs p.T778fs KIPAN 22 41553171 41553201 + Splice_Site DEL GAGTAATGTTTGATGTCACTTGTCTTTCTAG GAGTAATGTTTGATGTCACTTGTCTTTCTAG - TCGA-J7-A8I2-01A-12D-A35Z-10 TCGA-J7-A8I2-10A-01D-A35Z-10 g.chr22:41553171_41553201delGAGTAATGTTTGATGTCACTTGTCTTTCTAG c.3261_3290delGAGTAATGTTTGATGTCACTTGTCTTTCTAG c.(3259-3291)ccgagtaatgtttgatgtcacttgtctttctag>ccg p.SNV*CHLSF*1088fs KIPAN 22 41558757 41558757 + Frame_Shift_Del DEL A A - TCGA-GL-A59R-01A-11D-A26P-10 TCGA-GL-A59R-10A-01D-A26P-10 g.chr22:41558757delA c.3702delA c.(3700-3702)agafs p.R1234fs KIPAN 22 41572322 41572322 + Silent SNP T T C TCGA-B9-A8YH-01A-11D-A36X-10 TCGA-B9-A8YH-10A-01D-A370-10 g.chr22:41572322T>C c.4851T>C c.(4849-4851)ccT>ccC p.P1617P KIPAN 22 41572994 41572994 + Missense_Mutation SNP A A G TCGA-CJ-6030-01A-11D-1669-08 TCGA-CJ-6030-11A-01D-1669-08 g.chr22:41572994A>G c.5279A>G c.(5278-5280)aAg>aGg p.K1760R KIPAN 22 41573737 41573737 + Missense_Mutation SNP T T C TCGA-B0-4811-01A-01D-1501-10 TCGA-B0-4811-11A-02D-1501-10 g.chr22:41573737T>C c.6022T>C c.(6022-6024)Tct>Cct p.S2008P KIPAN 22 41574164 41574176 + Frame_Shift_Del DEL CACAGCAGCAACT CACAGCAGCAACT - TCGA-DW-7840-01A-11D-2136-08 TCGA-DW-7840-10A-01D-2136-08 g.chr22:41574164_41574176delCACAGCAGCAACT c.6449_6461delCACAGCAGCAACT c.(6448-6462)ccacagcagcaactcfs p.PQQQL2150fs KIPAN 22 41574312 41574312 + Silent SNP A A G TCGA-B0-5098-01A-01D-1421-08 TCGA-B0-5098-11A-01D-1421-08 g.chr22:41574312A>G c.6597A>G c.(6595-6597)ccA>ccG p.P2199P KIPAN 22 41574358 41574358 + Missense_Mutation SNP C C A TCGA-CZ-4859-01A-02D-1429-08 TCGA-CZ-4859-11A-01D-1429-08 g.chr22:41574358C>A c.6643C>A c.(6643-6645)Caa>Aaa p.Q2215K KIPAN 22 41574679 41574681 + In_Frame_Del DEL CCC CCC - TCGA-B3-4103-01A-01D-1458-08 TCGA-B3-4103-10A-01D-1458-08 g.chr22:41574679_41574681delCCC c.6964_6966delCCC c.(6964-6966)cccdel p.P2323del KIPAN 22 41574794 41574794 + Missense_Mutation SNP A A G TCGA-B8-5158-01A-01D-1421-08 TCGA-B8-5158-10A-01D-1421-08 g.chr22:41574794A>G c.7079A>G c.(7078-7080)gAa>gGa p.E2360G KIRC 22 41513594 41513594 + Missense_Mutation SNP C C A TCGA-B0-5713-01A-11D-1669-08 TCGA-B0-5713-11A-01D-1669-08 g.chr22:41513594C>A c.498C>A c.(496-498)aaC>aaA p.N166K KIRC 22 41536219 41536219 + Silent SNP T T C TCGA-AK-3428-01A-02D-1361-10 TCGA-AK-3428-10A-01D-1361-10 g.chr22:41536219T>C c.1836T>C c.(1834-1836)gcT>gcC p.A612A KIRC 22 41572994 41572994 + Missense_Mutation SNP A A G TCGA-CJ-6030-01A-11D-1669-08 TCGA-CJ-6030-11A-01D-1669-08 g.chr22:41572994A>G c.5279A>G c.(5278-5280)aAg>aGg p.K1760R KIRC 22 41573737 41573737 + Missense_Mutation SNP T T C TCGA-B0-4811-01A-01D-1501-10 TCGA-B0-4811-11A-02D-1501-10 g.chr22:41573737T>C c.6022T>C c.(6022-6024)Tct>Cct p.S2008P KIRC 22 41574312 41574312 + Silent SNP A A G TCGA-B0-5098-01A-01D-1421-08 TCGA-B0-5098-11A-01D-1421-08 g.chr22:41574312A>G c.6597A>G c.(6595-6597)ccA>ccG p.P2199P KIRC 22 41574358 41574358 + Missense_Mutation SNP C C A TCGA-CZ-4859-01A-02D-1429-08 TCGA-CZ-4859-11A-01D-1429-08 g.chr22:41574358C>A c.6643C>A c.(6643-6645)Caa>Aaa p.Q2215K KIRC 22 41574794 41574794 + Missense_Mutation SNP A A G TCGA-B8-5158-01A-01D-1421-08 TCGA-B8-5158-10A-01D-1421-08 g.chr22:41574794A>G c.7079A>G c.(7078-7080)gAa>gGa p.E2360G KIRP 22 41527606 41527606 + Silent SNP T T C TCGA-5P-A9K3-01A-11D-A42J-10 TCGA-5P-A9K3-10A-01D-A42M-10 g.chr22:41527606T>C c.1497T>C c.(1495-1497)tcT>tcC p.S499S KIRP 22 41542756 41542756 + Silent SNP T T C TCGA-UZ-A9PK-01A-11D-A382-10 TCGA-UZ-A9PK-10A-01D-A385-10 g.chr22:41542756T>C c.2067T>C c.(2065-2067)ccT>ccC p.P689P KIRP 22 41545134 41545134 + Frame_Shift_Del DEL A A - TCGA-Y8-A898-01A-11D-A34Z-10 TCGA-Y8-A898-10A-01D-A34Z-10 g.chr22:41545134delA c.2334delA c.(2332-2334)acafs p.T778fs KIRP 22 41553171 41553201 + Splice_Site DEL GAGTAATGTTTGATGTCACTTGTCTTTCTAG GAGTAATGTTTGATGTCACTTGTCTTTCTAG - TCGA-J7-A8I2-01A-12D-A35Z-10 TCGA-J7-A8I2-10A-01D-A35Z-10 g.chr22:41553171_41553201delGAGTAATGTTTGATGTCACTTGTCTTTCTAG c.3261_3290delGAGTAATGTTTGATGTCACTTGTCTTTCTAG c.(3259-3291)ccgagtaatgtttgatgtcacttgtctttctag>ccg p.SNV*CHLSF*1088fs KIRP 22 41558757 41558757 + Frame_Shift_Del DEL A A - TCGA-GL-A59R-01A-11D-A26P-10 TCGA-GL-A59R-10A-01D-A26P-10 g.chr22:41558757delA c.3702delA c.(3700-3702)agafs p.R1234fs KIRP 22 41572322 41572322 + Silent SNP T T C TCGA-B9-A8YH-01A-11D-A36X-10 TCGA-B9-A8YH-10A-01D-A370-10 g.chr22:41572322T>C c.4851T>C c.(4849-4851)ccT>ccC p.P1617P KIRP 22 41574164 41574176 + Frame_Shift_Del DEL CACAGCAGCAACT CACAGCAGCAACT - TCGA-DW-7840-01A-11D-2136-08 TCGA-DW-7840-10A-01D-2136-08 g.chr22:41574164_41574176delCACAGCAGCAACT c.6449_6461delCACAGCAGCAACT c.(6448-6462)ccacagcagcaactcfs p.PQQQL2150fs KIRP 22 41574679 41574681 + In_Frame_Del DEL CCC CCC - TCGA-B3-4103-01A-01D-1458-08 TCGA-B3-4103-10A-01D-1458-08 g.chr22:41574679_41574681delCCC c.6964_6966delCCC c.(6964-6966)cccdel p.P2323del LGG 22 41513608 41513608 + Missense_Mutation SNP C C T TCGA-P5-A77X-01A-11D-A32B-08 TCGA-P5-A77X-10A-01D-A329-08 g.chr22:41513608C>T c.512C>T c.(511-513)gCg>gTg p.A171V LGG 22 41523588 41523588 + Missense_Mutation SNP G G A TCGA-DU-A7TA-01A-11D-A33T-08 TCGA-DU-A7TA-10A-01D-A33W-08 g.chr22:41523588G>A c.1004G>A c.(1003-1005)cGc>cAc p.R335H LGG 22 41566461 41566461 + Silent SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr22:41566461T>C c.4338T>C c.(4336-4338)taT>taC p.Y1446Y LGG 22 41566476 41566476 + Silent SNP T T C TCGA-DB-A64V-01A-11D-A29Q-08 TCGA-DB-A64V-10A-01D-A29Q-08 g.chr22:41566476T>C c.4353T>C c.(4351-4353)caT>caC p.H1451H LGG 22 41574489 41574489 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr22:41574489G>T c.6774G>T c.(6772-6774)caG>caT p.Q2258H LGG 22 41574637 41574637 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr22:41574637C>T c.6922C>T c.(6922-6924)Cgc>Tgc p.R2308C LGG 22 41574836 41574836 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr22:41574836C>A c.7121C>A c.(7120-7122)tCt>tAt p.S2374Y LIHC 22 41513713 41513713 + Missense_Mutation SNP A A G TCGA-DD-A119-01A-11D-A12Z-10 TCGA-DD-A119-10A-01D-A12Z-10 g.chr22:41513713A>G c.617A>G c.(616-618)cAg>cGg p.Q206R LIHC 22 41523630 41523630 + Missense_Mutation SNP A A G TCGA-5C-A9VG-01A-11D-A36X-10 TCGA-5C-A9VG-10A-01D-A370-10 g.chr22:41523630A>G c.1046A>G c.(1045-1047)cAc>cGc p.H349R LIHC 22 41545769 41545769 + Missense_Mutation SNP A A G TCGA-DD-AAD3-01A-11D-A40R-10 TCGA-DD-AAD3-10A-01D-A40U-10 g.chr22:41545769A>G c.2384A>G c.(2383-2385)cAa>cGa p.Q795R LIHC 22 41547912 41547912 + Missense_Mutation SNP C C G TCGA-DD-AAE0-01A-11D-A40R-10 TCGA-DD-AAE0-10A-01D-A40U-10 g.chr22:41547912C>G c.2893C>G c.(2893-2895)Cag>Gag p.Q965E LIHC 22 41560092 41560092 + Missense_Mutation SNP A A T TCGA-DD-A1EE-01A-11D-A12Z-10 TCGA-DD-A1EE-10A-01D-A12Z-10 g.chr22:41560092A>T c.3764A>T c.(3763-3765)cAt>cTt p.H1255L LIHC 22 41560092 41560092 + Missense_Mutation SNP A A T TCGA-EP-A26S-01A-11D-A16V-10 TCGA-EP-A26S-10A-01D-A16V-10 g.chr22:41560092A>T c.3764A>T c.(3763-3765)cAt>cTt p.H1255L LIHC 22 41568575 41568575 + Missense_Mutation SNP T T A TCGA-G3-AAV2-01A-11D-A36X-10 TCGA-G3-AAV2-10A-01D-A370-10 g.chr22:41568575T>A c.4525T>A c.(4525-4527)Tgg>Agg p.W1509R LIHC 22 41569712 41569712 + Missense_Mutation SNP A A G TCGA-DD-AACH-01A-11D-A40R-10 TCGA-DD-AACH-10A-01D-A40U-10 g.chr22:41569712A>G c.4703A>G c.(4702-4704)aAg>aGg p.K1568R LIHC 22 41572904 41572904 + Missense_Mutation SNP C C A TCGA-EP-A2KB-01A-11D-A183-10 TCGA-EP-A2KB-10A-01D-A183-10 g.chr22:41572904C>A c.5189C>A c.(5188-5190)tCt>tAt p.S1730Y LIHC 22 41573037 41573037 + Missense_Mutation SNP A A T TCGA-EP-A2KA-01A-11D-A183-10 TCGA-EP-A2KA-10A-01D-A183-10 g.chr22:41573037A>T c.5322A>T c.(5320-5322)aaA>aaT p.K1774N LIHC 22 41574171 41574171 + Silent SNP G G A TCGA-2V-A95S-01A-11D-A36X-10 TCGA-2V-A95S-10D-01D-A370-10 g.chr22:41574171G>A c.6456G>A c.(6454-6456)caG>caA p.Q2152Q LIHC 22 41574679 41574679 + Frame_Shift_Del DEL C C - TCGA-DD-A1EG-01A-11D-A20W-10 TCGA-DD-A1EG-10A-01D-A20W-10 g.chr22:41574679delC c.6964delC c.(6964-6966)cccfs p.P2323fs LIHC 22 41574846 41574846 + Silent SNP T T C TCGA-GJ-A6C0-01A-12D-A30V-10 TCGA-GJ-A6C0-10A-01D-A30V-10 g.chr22:41574846T>C c.7131T>C c.(7129-7131)gcT>gcC p.A2377A LIHC 22 41574913 41574913 + Missense_Mutation SNP T T A TCGA-DD-AACX-01A-11D-A40R-10 TCGA-DD-AACX-10A-01D-A40U-10 g.chr22:41574913T>A c.7198T>A c.(7198-7200)Tca>Aca p.S2400T LUAD 22 41489047 41489047 + Silent SNP C C G TCGA-86-6851-01A-11D-1945-08 TCGA-86-6851-10A-01D-1946-08 g.chr22:41489047C>G c.39C>G c.(37-39)gcC>gcG p.A13A LUAD 22 41513609 41513609 + Silent SNP G G T TCGA-MP-A4TK-01A-11D-A24P-08 TCGA-MP-A4TK-10A-01D-A24P-08 g.chr22:41513609G>T c.513G>T c.(511-513)gcG>gcT p.A171A LUAD 22 41527619 41527619 + Missense_Mutation SNP C C T TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chr22:41527619C>T c.1510C>T c.(1510-1512)Cgg>Tgg p.R504W LUAD 22 41536235 41536235 + Missense_Mutation SNP G G A TCGA-NJ-A4YQ-01A-11D-A25L-08 TCGA-NJ-A4YQ-10A-01D-A25L-08 g.chr22:41536235G>A c.1852G>A c.(1852-1854)Gac>Aac p.D618N LUAD 22 41548347 41548347 + Missense_Mutation SNP G G T TCGA-78-8660-01A-11D-2393-08 TCGA-78-8660-10A-01D-2393-08 g.chr22:41548347G>T c.3135G>T c.(3133-3135)aaG>aaT p.K1045N LUAD 22 41556648 41556648 + Missense_Mutation SNP A A T TCGA-95-7567-01A-11D-2063-08 TCGA-95-7567-10A-01D-2063-08 g.chr22:41556648A>T c.3593A>T c.(3592-3594)tAt>tTt p.Y1198F LUAD 22 41564796 41564796 + Frame_Shift_Del DEL T T - TCGA-69-7974-01A-11D-2184-08 TCGA-69-7974-10A-01D-2184-08 g.chr22:41564796delT c.4097delT c.(4096-4098)attfs p.I1366fs LUAD 22 41566409 41566409 + Splice_Site SNP G G C TCGA-95-7043-01A-11D-1945-08 TCGA-95-7043-10A-01D-1946-08 g.chr22:41566409G>C c.e27-1 LUAD 22 41568503 41568503 + Splice_Site SNP G G T TCGA-64-5774-01A-01D-1625-08 TCGA-64-5774-10A-01D-1625-08 g.chr22:41568503G>T c.4453G>T c.(4453-4455)Gat>Tat p.D1485Y LUAD 22 41568563 41568563 + Nonsense_Mutation SNP G G T TCGA-55-6969-01A-11D-1945-08 TCGA-55-6969-11A-01D-1945-08 g.chr22:41568563G>T c.4513G>T c.(4513-4515)Gag>Tag p.E1505* LUAD 22 41572505 41572505 + Silent SNP G G A TCGA-17-Z033-01A-01W-0746-08 TCGA-17-Z033-11A-01W-0746-08 g.chr22:41572505G>A c.5034G>A c.(5032-5034)gaG>gaA p.E1678E LUAD 22 41573107 41573107 + Nonsense_Mutation SNP G G T TCGA-17-Z033-01A-01W-0746-08 TCGA-17-Z033-11A-01W-0746-08 g.chr22:41573107G>T c.5392G>T c.(5392-5394)Gag>Tag p.E1798* LUAD 22 41573426 41573426 + Missense_Mutation SNP A A C TCGA-91-8499-01A-11D-2393-08 TCGA-91-8499-10A-01D-2393-08 g.chr22:41573426A>C c.5711A>C c.(5710-5712)cAg>cCg p.Q1904P LUAD 22 41573857 41573857 + Nonsense_Mutation SNP C C T TCGA-17-Z026-01A-01W-0746-08 TCGA-17-Z026-11A-01W-0746-08 g.chr22:41573857C>T c.6142C>T c.(6142-6144)Caa>Taa p.Q2048* LUAD 22 41574498 41574498 + Silent SNP G G A TCGA-91-6848-01A-11D-1945-08 TCGA-91-6848-11A-01D-1945-08 g.chr22:41574498G>A c.6783G>A c.(6781-6783)caG>caA p.Q2261Q LUSC 22 41521907 41521907 + Missense_Mutation SNP T T G TCGA-37-3783-01A-01D-1267-08 TCGA-37-3783-10A-01D-1267-08 g.chr22:41521907T>G c.769T>G c.(769-771)Tat>Gat p.Y257D LUSC 22 41565505 41565505 + Splice_Site SNP A A G TCGA-18-3419-01A-01D-0983-08 TCGA-18-3419-11A-01D-0983-08 g.chr22:41565505A>G c.e26-1 LUSC 22 41565527 41565527 + Missense_Mutation SNP T T C TCGA-56-1622-01A-01D-1521-08 TCGA-56-1622-11A-01D-1521-08 g.chr22:41565527T>C c.4193T>C c.(4192-4194)cTc>cCc p.L1398P LUSC 22 41565529 41565529 + Missense_Mutation SNP G G A TCGA-21-5786-01A-01D-1632-08 TCGA-21-5786-10A-01D-1632-08 g.chr22:41565529G>A c.4195G>A c.(4195-4197)Gat>Aat p.D1399N LUSC 22 41565529 41565529 + Missense_Mutation SNP G G A TCGA-66-2763-01A-01D-1522-08 TCGA-66-2763-11A-01D-1522-08 g.chr22:41565529G>A c.4195G>A c.(4195-4197)Gat>Aat p.D1399N LUSC 22 41565575 41565575 + Missense_Mutation SNP A A G TCGA-37-3783-01A-01D-1267-08 TCGA-37-3783-10A-01D-1267-08 g.chr22:41565575A>G c.4241A>G c.(4240-4242)tAt>tGt p.Y1414C LUSC 22 41572364 41572364 + Silent SNP C C T TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr22:41572364C>T c.4893C>T c.(4891-4893)ctC>ctT p.L1631L LUSC 22 41573348 41573348 + Missense_Mutation SNP C C A TCGA-60-2713-01A-01D-1522-08 TCGA-60-2713-11A-01D-1522-08 g.chr22:41573348C>A c.5633C>A c.(5632-5634)aCc>aAc p.T1878N LUSC 22 41574082 41574082 + Missense_Mutation SNP G G T TCGA-66-2773-01A-01D-1267-08 TCGA-66-2773-11A-01D-1267-08 g.chr22:41574082G>T c.6367G>T c.(6367-6369)Ggg>Tgg p.G2123W LUSC 22 41574090 41574090 + Missense_Mutation SNP C C A TCGA-22-4595-01A-01D-1267-08 TCGA-22-4595-11A-01D-1267-08 g.chr22:41574090C>A c.6375C>A c.(6373-6375)caC>caA p.H2125Q LUSC 22 41574204 41574204 + Silent SNP C C T TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr22:41574204C>T c.6489C>T c.(6487-6489)ccC>ccT p.P2163P OV 22 41537079 41537079 + Missense_Mutation SNP A A G TCGA-36-2542-01A-01D-1526-09 TCGA-36-2542-10A-01D-1526-09 g.chr22:41537079A>G c.1906A>G c.(1906-1908)Aaa>Gaa p.K636E OV 22 41564512 41564512 + Nonsense_Mutation SNP C C T TCGA-24-1471-01A-01W-0551-08 TCGA-24-1471-10A-01W-0551-08 g.chr22:41564512C>T c.3934C>T c.(3934-3936)Cga>Tga p.R1312* PAAD 22 41513320 41513320 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr22:41513320C>T c.224C>T c.(223-225)gCt>gTt p.A75V PAAD 22 41533755 41533755 + Missense_Mutation SNP A A G TCGA-IB-7885-01A-11D-2154-08 TCGA-IB-7885-10A-01D-2154-08 g.chr22:41533755A>G c.1721A>G c.(1720-1722)gAt>gGt p.D574G PAAD 22 41542773 41542773 + Missense_Mutation SNP G G A TCGA-2J-AABO-01A-21D-A40W-08 TCGA-2J-AABO-10A-01D-A40W-08 g.chr22:41542773G>A c.2084G>A c.(2083-2085)cGt>cAt p.R695H PAAD 22 41572357 41572357 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr22:41572357C>T c.4886C>T c.(4885-4887)gCg>gTg p.A1629V PAAD 22 41573306 41573306 + Missense_Mutation SNP C C G TCGA-FB-AAQ6-01A-11D-A40W-08 TCGA-FB-AAQ6-11A-11D-A40W-08 g.chr22:41573306C>G c.5591C>G c.(5590-5592)aCc>aGc p.T1864S PAAD 22 41574502 41574502 + Nonsense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr22:41574502C>T c.6787C>T c.(6787-6789)Cga>Tga p.R2263* PRAD 22 41525896 41525896 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr22:41525896G>A c.1171G>A c.(1171-1173)Gca>Aca p.A391T PRAD 22 41536147 41536147 + Silent SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr22:41536147C>T c.1764C>T c.(1762-1764)gtC>gtT p.V588V PRAD 22 41554480 41554480 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr22:41554480C>T c.3566C>T c.(3565-3567)gCc>gTc p.A1189V PRAD 22 41573200 41573200 + Missense_Mutation SNP C C T TCGA-HC-7817-01B-11D-A29Q-08 TCGA-HC-7817-10A-01D-A29Q-08 g.chr22:41573200C>T c.5485C>T c.(5485-5487)Cgc>Tgc p.R1829C PRAD 22 41573205 41573205 + Missense_Mutation SNP G G T TCGA-J4-A67M-01A-11D-A30E-08 TCGA-J4-A67M-10A-01D-A30H-08 g.chr22:41573205G>T c.5490G>T c.(5488-5490)agG>agT p.R1830S PRAD 22 41573944 41573944 + Missense_Mutation SNP A A G TCGA-KK-A59V-01A-11D-A29Q-08 TCGA-KK-A59V-11A-11D-A29Q-08 g.chr22:41573944A>G c.6229A>G c.(6229-6231)Aac>Gac p.N2077D PRAD 22 41573977 41573977 + Missense_Mutation SNP C C T TCGA-G9-6366-01A-11D-2114-08 TCGA-G9-6366-10A-01D-2115-08 g.chr22:41573977C>T c.6262C>T c.(6262-6264)Cgg>Tgg p.R2088W PRAD 22 41574665 41574665 + Missense_Mutation SNP G G A TCGA-ZG-A8QW-01A-11D-A377-08 TCGA-ZG-A8QW-10A-01D-A37A-08 g.chr22:41574665G>A c.6950G>A c.(6949-6951)cGg>cAg p.R2317Q READ 22 41513646 41513646 + Nonsense_Mutation SNP C C T TCGA-DC-6682-01A-11D-1826-10 TCGA-DC-6682-10A-01D-1826-10 g.chr22:41513646C>T c.550C>T c.(550-552)Caa>Taa p.Q184* READ 22 41523526 41523526 + Silent SNP C C T TCGA-DY-A1DD-01A-21D-A152-10 TCGA-DY-A1DD-10A-01D-A152-10 g.chr22:41523526C>T c.942C>T c.(940-942)ggC>ggT p.G314G READ 22 41545903 41545903 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr22:41545903C>A c.2518C>A c.(2518-2520)Ccc>Acc p.P840T READ 22 41548251 41548251 + Silent SNP A A G TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr22:41548251A>G c.3039A>G c.(3037-3039)gaA>gaG p.E1013E READ 22 41548253 41548253 + Missense_Mutation SNP A A G TCGA-DC-6682-01A-11D-1826-10 TCGA-DC-6682-10A-01D-1826-10 g.chr22:41548253A>G c.3041A>G c.(3040-3042)gAg>gGg p.E1014G READ 22 41564512 41564512 + Nonsense_Mutation SNP C C T TCGA-G5-6641-01A-11D-1826-10 TCGA-G5-6641-10A-01D-1826-10 g.chr22:41564512C>T c.3934C>T c.(3934-3936)Cga>Tga p.R1312* READ 22 41569717 41569717 + Missense_Mutation SNP A A G TCGA-CI-6619-01B-11D-1826-10 TCGA-CI-6619-10A-01D-1826-10 g.chr22:41569717A>G c.4708A>G c.(4708-4710)Aaa>Gaa p.K1570E READ 22 41569718 41569718 + Missense_Mutation SNP A A G TCGA-AG-3732-01A-11D-1657-10 TCGA-AG-3732-11A-01D-1657-10 g.chr22:41569718A>G c.4709A>G c.(4708-4710)aAa>aGa p.K1570R READ 22 41572266 41572266 + Missense_Mutation SNP C C T TCGA-G5-6235-01A-11D-1733-10 TCGA-G5-6235-10A-01D-1733-10 g.chr22:41572266C>T c.4795C>T c.(4795-4797)Cgc>Tgc p.R1599C READ 22 41572350 41572350 + Missense_Mutation SNP C C T TCGA-EI-6510-01A-11D-1733-10 TCGA-EI-6510-10A-01D-1733-10 g.chr22:41572350C>T c.4879C>T c.(4879-4881)Cgg>Tgg p.R1627W READ 22 41572510 41572510 + Missense_Mutation SNP G G A TCGA-F5-6813-01A-11D-1826-10 TCGA-F5-6813-10A-01D-1826-10 g.chr22:41572510G>A c.5039G>A c.(5038-5040)cGc>cAc p.R1680H READ 22 41573425 41573425 + Nonsense_Mutation SNP C C T TCGA-AF-2687-01A-02D-1733-10 TCGA-AF-2687-10A-01D-1733-10 g.chr22:41573425C>T c.5710C>T c.(5710-5712)Cag>Tag p.Q1904* READ 22 41574238 41574238 + Missense_Mutation SNP A A G TCGA-G5-6235-01A-11D-1733-10 TCGA-G5-6235-10A-01D-1733-10 g.chr22:41574238A>G c.6523A>G c.(6523-6525)Atg>Gtg p.M2175V READ 22 41574377 41574377 + Missense_Mutation SNP C C T TCGA-G5-6235-01A-11D-1733-10 TCGA-G5-6235-10A-01D-1733-10 g.chr22:41574377C>T c.6662C>T c.(6661-6663)cCa>cTa p.P2221L READ 22 41574679 41574679 + Frame_Shift_Del DEL C C - TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr22:41574679delC c.6964delC c.(6964-6966)cccfs p.P2323fs READ 22 41574836 41574836 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr22:41574836C>A c.7121C>A c.(7120-7122)tCt>tAt p.S2374Y SARC 22 41513219 41513219 + Silent SNP C C T TCGA-DX-A1KX-01A-22D-A24N-09 TCGA-DX-A1KX-10A-01D-A24N-09 g.chr22:41513219C>T c.123C>T c.(121-123)caC>caT p.H41H SARC 22 41513453 41513453 + Missense_Mutation SNP T T A TCGA-QC-A7B5-01A-11D-A33E-09 TCGA-QC-A7B5-11A-11D-A33H-09 g.chr22:41513453T>A c.357T>A c.(355-357)aaT>aaA p.N119K SARC 22 41513493 41513493 + Missense_Mutation SNP T T G TCGA-DX-AB2Q-01A-11D-A38Z-09 TCGA-DX-AB2Q-10A-01D-A38Z-09 g.chr22:41513493T>G c.397T>G c.(397-399)Tct>Gct p.S133A SKCM 22 41513565 41513565 + Missense_Mutation SNP C C G TCGA-EE-A182-06A-11D-A196-08 TCGA-EE-A182-10A-01D-A198-08 g.chr22:41513565C>G c.469C>G c.(469-471)Cca>Gca p.P157A SKCM 22 41513566 41513566 + Missense_Mutation SNP C C T TCGA-EE-A182-06A-11D-A196-08 TCGA-EE-A182-10A-01D-A198-08 g.chr22:41513566C>T c.470C>T c.(469-471)cCa>cTa p.P157L SKCM 22 41513752 41513752 + Missense_Mutation SNP T T C TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr22:41513752T>C c.656T>C c.(655-657)cTg>cCg p.L219P SKCM 22 41523662 41523662 + Missense_Mutation SNP G G A TCGA-EE-A29L-06A-12D-A196-08 TCGA-EE-A29L-10A-01D-A198-08 g.chr22:41523662G>A c.1078G>A c.(1078-1080)Gaa>Aaa p.E360K SKCM 22 41527608 41527608 + Missense_Mutation SNP C C T TCGA-EE-A3AA-06A-11D-A196-08 TCGA-EE-A3AA-10A-01D-A198-08 g.chr22:41527608C>T c.1499C>T c.(1498-1500)cCc>cTc p.P500L SKCM 22 41537070 41537070 + Silent SNP C C T TCGA-EE-A2A6-06A-11D-A197-08 TCGA-EE-A2A6-10A-01D-A199-08 g.chr22:41537070C>T c.1897C>T c.(1897-1899)Cta>Tta p.L633L SKCM 22 41545778 41545778 + Missense_Mutation SNP G G A TCGA-EB-A5UN-06A-11D-A30X-08 TCGA-EB-A5UN-10A-01D-A30X-08 g.chr22:41545778G>A c.2393G>A c.(2392-2394)aGt>aAt p.S798N SKCM 22 41545984 41545984 + Missense_Mutation SNP C C T TCGA-D3-A5GN-06A-11D-A27K-08 TCGA-D3-A5GN-10A-01D-A27N-08 g.chr22:41545984C>T c.2599C>T c.(2599-2601)Cct>Tct p.P867S SKCM 22 41551054 41551054 + Silent SNP C C T TCGA-EE-A2GS-06A-12D-A197-08 TCGA-EE-A2GS-10A-01D-A199-08 g.chr22:41551054C>T c.3198C>T c.(3196-3198)taC>taT p.Y1066Y SKCM 22 41553271 41553271 + Silent SNP T T C TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr22:41553271T>C c.3360T>C c.(3358-3360)gaT>gaC p.D1120D SKCM 22 41556650 41556650 + Missense_Mutation SNP C C T TCGA-GF-A4EO-06A-12D-A24R-08 TCGA-GF-A4EO-10A-01D-A24R-08 g.chr22:41556650C>T c.3595C>T c.(3595-3597)Cat>Tat p.H1199Y SKCM 22 41564759 41564759 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr22:41564759C>T c.4060C>T c.(4060-4062)Cca>Tca p.P1354S SKCM 22 41564798 41564798 + Missense_Mutation SNP G G T TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr22:41564798G>T c.4099G>T c.(4099-4101)Gat>Tat p.D1367Y SKCM 22 41572330 41572330 + Missense_Mutation SNP C C T TCGA-EE-A17X-06A-11D-A197-08 TCGA-EE-A17X-10A-01D-A199-08 g.chr22:41572330C>T c.4859C>T c.(4858-4860)cCc>cTc p.P1620L SKCM 22 41572331 41572331 + Silent SNP C C T TCGA-EE-A17X-06A-11D-A197-08 TCGA-EE-A17X-10A-01D-A199-08 g.chr22:41572331C>T c.4860C>T c.(4858-4860)ccC>ccT p.P1620P SKCM 22 41572350 41572350 + Missense_Mutation SNP C C T TCGA-D3-A2JF-06A-11D-A196-08 TCGA-D3-A2JF-10A-01D-A198-08 g.chr22:41572350C>T c.4879C>T c.(4879-4881)Cgg>Tgg p.R1627W SKCM 22 41572389 41572389 + Nonsense_Mutation SNP G G T TCGA-EE-A3JB-06A-11D-A21A-08 TCGA-EE-A3JB-10A-01D-A21A-08 g.chr22:41572389G>T c.4918G>T c.(4918-4920)Gag>Tag p.E1640* SKCM 22 41572463 41572463 + Silent SNP C C T TCGA-D3-A3MU-06A-11D-A21A-08 TCGA-D3-A3MU-10A-01D-A21A-08 g.chr22:41572463C>T c.4992C>T c.(4990-4992)gaC>gaT p.D1664D SKCM 22 41573197 41573197 + Missense_Mutation SNP C C T TCGA-EE-A2GL-06A-11D-A196-08 TCGA-EE-A2GL-10A-01D-A198-08 g.chr22:41573197C>T c.5482C>T c.(5482-5484)Ctt>Ttt p.L1828F SKCM 22 41573345 41573345 + Missense_Mutation SNP C C T TCGA-FS-A1ZK-06A-11D-A197-08 TCGA-FS-A1ZK-10A-01D-A199-08 g.chr22:41573345C>T c.5630C>T c.(5629-5631)cCt>cTt p.P1877L SKCM 22 41573662 41573662 + Missense_Mutation SNP G G A TCGA-EE-A2GO-06A-11D-A196-08 TCGA-EE-A2GO-10A-01D-A198-08 g.chr22:41573662G>A c.5947G>A c.(5947-5949)Ggg>Agg p.G1983R SKCM 22 41573875 41573875 + Missense_Mutation SNP C C T TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr22:41573875C>T c.6160C>T c.(6160-6162)Ctt>Ttt p.L2054F SKCM 22 41574339 41574339 + Missense_Mutation SNP T T A TCGA-ER-A42L-06A-11D-A24R-08 TCGA-ER-A42L-10A-01D-A24R-08 g.chr22:41574339T>A c.6624T>A c.(6622-6624)caT>caA p.H2208Q SKCM 22 41574341 41574341 + Missense_Mutation SNP A A T TCGA-ER-A42L-06A-11D-A24R-08 TCGA-ER-A42L-10A-01D-A24R-08 g.chr22:41574341A>T c.6626A>T c.(6625-6627)aAc>aTc p.N2209I

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation AML-US 22 41553402 41553402 single base substitution G A missense_variant C1164Y 3491G>A AML-US 22 41560133 41560133 single base substitution G T stop_gained G1269* 3805G>T AML-US 22 41562672 41562672 single base substitution T A splice_donor_variant BLCA-CN 22 41513289 41513289 single base substitution C T stop_gained Q65* 193C>T BLCA-CN 22 41545855 41545855 single base substitution C T stop_gained Q824* 2470C>T BLCA-CN 22 41546005 41546005 single base substitution C T stop_gained Q874* 2620C>T BLCA-CN 22 41565529 41565529 single base substitution G A missense_variant D1399N 4195G>A BLCA-CN 22 41566475 41566475 single base substitution A T missense_variant H1451L 4352A>T BLCA-CN 22 41568504 41568504 single base substitution A T missense_variant D1485V 4454A>T BLCA-CN 22 41568611 41568611 single base substitution G C missense_variant E1521Q 4561G>C BLCA-CN 22 41569671 41569671 single base substitution G C missense_variant K1554N 4662G>C BLCA-CN 22 41572350 41572350 single base substitution C T missense_variant R1627W 4879C>T BLCA-CN 22 41574477 41574477 single base substitution T G synonymous_variant G2254G 6762T>G BLCA-US 22 41556722 41556722 single base substitution C G missense_variant Q1223E 3667C>G BLCA-US 22 41573079 41573079 single base substitution C G synonymous_variant L1788L 5364C>G BLCA-US 22 41573838 41573838 single base substitution C G synonymous_variant L2041L 6123C>G BLCA-US 22 41573889 41573889 single base substitution C G synonymous_variant L2058L 6174C>G BOCA-FR 22 41491202 41491202 single base substitution T G intron_variant BRCA-EU 22 41483040 41483040 single base substitution G C upstream_gene_variant BRCA-EU 22 41483304 41483304 single base substitution C T upstream_gene_variant BRCA-EU 22 41483429 41483433 deletion of <=200bp CAGGG - upstream_gene_variant BRCA-EU 22 41486259 41486259 single base substitution G A upstream_gene_variant BRCA-EU 22 41486675 41486675 single base substitution C T upstream_gene_variant BRCA-EU 22 41486868 41486868 single base substitution G A upstream_gene_variant BRCA-EU 22 41487122 41487122 single base substitution C T upstream_gene_variant BRCA-EU 22 41487340 41487340 single base substitution G A upstream_gene_variant BRCA-EU 22 41487779 41487779 single base substitution A G upstream_gene_variant BRCA-EU 22 41488319 41488319 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant BRCA-EU 22 41488567 41488567 single base substitution C G 5_prime_UTR_variant BRCA-EU 22 41489030 41489030 single base substitution C T missense_variant P8S 22C>T BRCA-EU 22 41489079 41489079 single base substitution C T missense_variant S24L 71C>T BRCA-EU 22 41489446 41489446 single base substitution A T intron_variant BRCA-EU 22 41490500 41490500 single base substitution C T intron_variant BRCA-EU 22 41490592 41490592 single base substitution C T intron_variant BRCA-EU 22 41491639 41491639 single base substitution T A intron_variant BRCA-EU 22 41493425 41493425 single base substitution C G intron_variant BRCA-EU 22 41494718 41494718 single base substitution A T intron_variant BRCA-EU 22 41495635 41495635 deletion of <=200bp T - intron_variant BRCA-EU 22 41496605 41496605 single base substitution T C intron_variant BRCA-EU 22 41497667 41497667 single base substitution G T intron_variant BRCA-EU 22 41499649 41499649 single base substitution G T intron_variant BRCA-EU 22 41500733 41500733 single base substitution A G intron_variant BRCA-EU 22 41502365 41502365 single base substitution C G intron_variant BRCA-EU 22 41502594 41502594 single base substitution G C intron_variant BRCA-EU 22 41505663 41505663 single base substitution T C intron_variant BRCA-EU 22 41505859 41505859 single base substitution C G intron_variant BRCA-EU 22 41509585 41509585 single base substitution C G intron_variant BRCA-EU 22 41510321 41510321 single base substitution G T intron_variant BRCA-EU 22 41510484 41510484 deletion of <=200bp G - intron_variant BRCA-EU 22 41510811 41510811 single base substitution A C intron_variant BRCA-EU 22 41511269 41511269 single base substitution T A intron_variant BRCA-EU 22 41511270 41511270 single base substitution G A intron_variant BRCA-EU 22 41512422 41512422 single base substitution A G intron_variant BRCA-EU 22 41516317 41516317 single base substitution C G intron_variant BRCA-EU 22 41516614 41516614 single base substitution G T intron_variant BRCA-EU 22 41517316 41517316 single base substitution G A intron_variant BRCA-EU 22 41517996 41517996 single base substitution T C intron_variant BRCA-EU 22 41519481 41519481 single base substitution A G intron_variant BRCA-EU 22 41519906 41519906 single base substitution T A intron_variant BRCA-EU 22 41520017 41520017 single base substitution C G intron_variant BRCA-EU 22 41520912 41520912 single base substitution G C intron_variant BRCA-EU 22 41521751 41521751 single base substitution G C intron_variant BRCA-EU 22 41521754 41521754 single base substitution G A intron_variant BRCA-EU 22 41522999 41522999 single base substitution C T intron_variant BRCA-EU 22 41523685 41523685 single base substitution C G synonymous_variant P367P 1101C>G BRCA-EU 22 41523889 41523889 single base substitution G A intron_variant BRCA-EU 22 41524020 41524020 single base substitution C T intron_variant BRCA-EU 22 41524023 41524023 single base substitution C T intron_variant BRCA-EU 22 41525092 41525092 single base substitution G A intron_variant BRCA-EU 22 41529179 41529179 single base substitution G C intron_variant BRCA-EU 22 41530483 41530483 single base substitution C T intron_variant BRCA-EU 22 41530757 41530757 single base substitution G A intron_variant BRCA-EU 22 41531519 41531519 single base substitution C G intron_variant BRCA-EU 22 41532265 41532265 single base substitution C T intron_variant BRCA-EU 22 41536991 41536991 single base substitution G A intron_variant BRCA-EU 22 41537349 41537349 single base substitution T G intron_variant BRCA-EU 22 41538427 41538427 single base substitution G A intron_variant BRCA-EU 22 41538759 41538759 single base substitution G T intron_variant BRCA-EU 22 41539180 41539180 single base substitution A G intron_variant BRCA-EU 22 41540601 41540601 single base substitution T A intron_variant BRCA-EU 22 41545568 41545568 single base substitution C G intron_variant BRCA-EU 22 41547976 41547976 single base substitution A T missense_variant Q986L 2957A>T BRCA-EU 22 41548523 41548523 single base substitution T C intron_variant BRCA-EU 22 41549006 41549006 single base substitution C T intron_variant BRCA-EU 22 41554533 41554533 single base substitution C T intron_variant BRCA-EU 22 41555217 41555217 single base substitution C T intron_variant BRCA-EU 22 41555456 41555456 single base substitution G C intron_variant BRCA-EU 22 41556504 41556504 single base substitution G T intron_variant BRCA-EU 22 41557082 41557082 single base substitution C T intron_variant BRCA-EU 22 41559746 41559746 single base substitution A G intron_variant BRCA-EU 22 41560663 41560663 single base substitution G A intron_variant BRCA-EU 22 41561437 41561437 single base substitution C G intron_variant BRCA-EU 22 41564396 41564396 single base substitution T C intron_variant BRCA-EU 22 41564818 41564818 single base substitution C A missense_variant F1373L 4119C>A BRCA-EU 22 41565562 41565562 single base substitution A T missense_variant R1410W 4228A>T BRCA-EU 22 41567375 41567375 single base substitution C T intron_variant BRCA-EU 22 41567537 41567537 single base substitution C T intron_variant BRCA-EU 22 41567866 41567866 single base substitution C G intron_variant BRCA-EU 22 41568031 41568031 single base substitution C A intron_variant BRCA-EU 22 41568574 41568574 single base substitution C G missense_variant F1508L 4524C>G BRCA-EU 22 41568731 41568731 single base substitution C G intron_variant BRCA-EU 22 41569164 41569164 single base substitution A T intron_variant BRCA-EU 22 41569569 41569569 single base substitution A G intron_variant BRCA-EU 22 41570483 41570483 single base substitution C T intron_variant BRCA-EU 22 41570597 41570597 single base substitution T A intron_variant BRCA-EU 22 41571222 41571222 single base substitution C G intron_variant BRCA-EU 22 41574133 41574133 single base substitution G A missense_variant V2140I 6418G>A BRCA-EU 22 41577012 41577012 single base substitution G C downstream_gene_variant BRCA-EU 22 41578655 41578655 single base substitution G A downstream_gene_variant BRCA-EU 22 41580362 41580362 single base substitution G C downstream_gene_variant BRCA-EU 22 41580456 41580456 single base substitution A C downstream_gene_variant BRCA-FR 22 41488319 41488319 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant BRCA-FR 22 41489030 41489030 single base substitution C T missense_variant P8S 22C>T BRCA-FR 22 41489079 41489079 single base substitution C T missense_variant S24L 71C>T BRCA-FR 22 41516317 41516317 single base substitution C G intron_variant BRCA-FR 22 41537322 41537322 single base substitution C G intron_variant BRCA-FR 22 41543584 41543584 single base substitution T C intron_variant BRCA-FR 22 41546463 41546463 single base substitution G A intron_variant BRCA-FR 22 41549006 41549006 single base substitution C T intron_variant BRCA-FR 22 41554533 41554533 single base substitution C T intron_variant BRCA-FR 22 41556504 41556504 single base substitution G T intron_variant BRCA-FR 22 41567375 41567375 single base substitution C T intron_variant BRCA-FR 22 41568574 41568574 single base substitution C G missense_variant F1508L 4524C>G BRCA-FR 22 41571222 41571222 single base substitution C G intron_variant BRCA-KR 22 41558709 41558709 single base substitution T G intron_variant BRCA-UK 22 41517996 41517996 single base substitution T C intron_variant BRCA-UK 22 41536237 41536237 single base substitution C G missense_variant D618E 1854C>G BRCA-UK 22 41542779 41542779 single base substitution G A missense_variant S697N 2090G>A BRCA-UK 22 41547976 41547976 single base substitution A T missense_variant Q986L 2957A>T BRCA-US 22 41489026 41489026 single base substitution G A synonymous_variant V6V 18G>A BRCA-US 22 41521913 41521913 single base substitution C T stop_gained Q259* 775C>T BRCA-US 22 41523564 41523564 single base substitution C T missense_variant A327V 980C>T BRCA-US 22 41527458 41527458 single base substitution C T missense_variant A450V 1349C>T BRCA-US 22 41527549 41527549 single base substitution G A missense_variant M480I 1440G>A BRCA-US 22 41527610 41527610 insertion of <=200bp - G frameshift_variant Q501A? BRCA-US 22 41545099 41545099 single base substitution C T stop_gained Q767* 2299C>T BRCA-US 22 41545883 41545883 single base substitution C T missense_variant S833L 2498C>T BRCA-US 22 41564860 41564860 single base substitution A C synonymous_variant P1387P 4161A>C BRCA-US 22 41566475 41566475 single base substitution A C missense_variant H1451P 4352A>C BRCA-US 22 41566525 41566525 deletion of <=200bp A - frameshift_variant K1468 BRCA-US 22 41568658 41568658 single base substitution A T missense_variant E1536D 4608A>T BRCA-US 22 41572386 41572386 single base substitution C T synonymous_variant L1639L 4915C>T BRCA-US 22 41573243 41573243 single base substitution A C missense_variant Q1843P 5528A>C BRCA-US 22 41573463 41573463 single base substitution A C synonymous_variant P1916P 5748A>C BRCA-US 22 41573569 41573569 single base substitution A G missense_variant I1952V 5854A>G BRCA-US 22 41573738 41573738 single base substitution C T missense_variant S2008F 6023C>T BTCA-JP 22 41489174 41489175 deletion of <=200bp TT - intron_variant BTCA-JP 22 41513219 41513219 single base substitution C T synonymous_variant H41H 123C>T BTCA-JP 22 41547877 41547877 single base substitution A G missense_variant N953S 2858A>G BTCA-JP 22 41553256 41553256 single base substitution G T missense_variant W1115C 3345G>T BTCA-JP 22 41553293 41553293 single base substitution G A missense_variant A1128T 3382G>A BTCA-JP 22 41554595 41554595 single base substitution A G intron_variant BTCA-JP 22 41556639 41556639 single base substitution C T splice_region_variant BTCA-JP 22 41573047 41573047 single base substitution G C missense_variant G1778R 5332G>C BTCA-JP 22 41573646 41573646 insertion of <=200bp - T frameshift_variant S1977S? CESC-US 22 41489064 41489064 single base substitution C G stop_gained S19* 56C>G CESC-US 22 41521980 41521980 single base substitution C G stop_gained S281* 842C>G CESC-US 22 41523536 41523536 single base substitution C G missense_variant P318A 952C>G CESC-US 22 41525927 41525927 single base substitution C G stop_gained S401* 1202C>G CESC-US 22 41527552 41527552 single base substitution G A synonymous_variant P481P 1443G>A CESC-US 22 41533715 41533715 single base substitution C T stop_gained Q561* 1681C>T CESC-US 22 41537053 41537053 single base substitution C T missense_variant A627V 1880C>T CESC-US 22 41537115 41537115 single base substitution C T stop_gained R648* 1942C>T CESC-US 22 41543930 41543930 single base substitution C T stop_gained Q741* 2221C>T CESC-US 22 41545129 41545129 single base substitution G A missense_variant V777I 2329G>A CESC-US 22 41545822 41545822 single base substitution C T stop_gained Q813* 2437C>T CESC-US 22 41547874 41547874 single base substitution C G stop_gained S952* 2855C>G CESC-US 22 41556727 41556727 single base substitution G A splice_donor_variant CESC-US 22 41558764 41558764 single base substitution G T missense_variant D1237Y 3709G>T CESC-US 22 41562602 41562602 single base substitution G C splice_acceptor_variant CESC-US 22 41562645 41562645 single base substitution G T missense_variant R1283S 3849G>T CESC-US 22 41564513 41564513 single base substitution G A missense_variant R1312Q 3935G>A CESC-US 22 41565529 41565529 single base substitution G A missense_variant D1399N 4195G>A CESC-US 22 41569751 41569751 single base substitution C T missense_variant S1581L 4742C>T CESC-US 22 41572405 41572405 single base substitution G A missense_variant R1645Q 4934G>A CESC-US 22 41572870 41572870 single base substitution C T stop_gained Q1719* 5155C>T CESC-US 22 41574358 41574358 single base substitution C T stop_gained Q2215* 6643C>T CESC-US 22 41574469 41574469 single base substitution G T stop_gained E2252* 6754G>T CLLE-ES 22 41506132 41506132 single base substitution C T intron_variant CLLE-ES 22 41523394 41523394 single base substitution A C intron_variant CLLE-ES 22 41529160 41529160 single base substitution C G intron_variant CLLE-ES 22 41552935 41552935 single base substitution A G intron_variant CLLE-ES 22 41573083 41573083 single base substitution T G missense_variant C1790G 5368T>G COAD-US 22 41513540 41513540 single base substitution G A synonymous_variant T148T 444G>A COAD-US 22 41526008 41526008 single base substitution G A splice_donor_variant COAD-US 22 41527620 41527620 single base substitution G T missense_variant R504L 1511G>T COAD-US 22 41533793 41533793 single base substitution C T missense_variant L587F 1759C>T COAD-US 22 41536167 41536167 single base substitution C T missense_variant P595L 1784C>T COAD-US 22 41547864 41547864 single base substitution G T stop_gained G949* 2845G>T COAD-US 22 41553327 41553327 single base substitution A G missense_variant Y1139C 3416A>G COAD-US 22 41560055 41560055 single base substitution A T splice_acceptor_variant COAD-US 22 41560059 41560059 single base substitution T G missense_variant F1244C 3731T>G COAD-US 22 41562627 41562627 single base substitution G T missense_variant K1277N 3831G>T COAD-US 22 41572908 41572908 single base substitution C T synonymous_variant R1731R 5193C>T COAD-US 22 41573046 41573046 single base substitution C T synonymous_variant G1777G 5331C>T COAD-US 22 41573200 41573200 single base substitution C T missense_variant R1829C 5485C>T COAD-US 22 41573577 41573577 single base substitution C T synonymous_variant H1954H 5862C>T COAD-US 22 41574487 41574487 single base substitution C T stop_gained Q2258* 6772C>T COCA-CN 22 41489222 41489222 single base substitution T A intron_variant COCA-CN 22 41513608 41513608 single base substitution C T missense_variant A171V 512C>T COCA-CN 22 41523739 41523739 single base substitution C T synonymous_variant G385G 1155C>T COCA-CN 22 41525996 41525996 single base substitution G T missense_variant R424I 1271G>T COCA-CN 22 41531900 41531900 single base substitution A C missense_variant N538H 1612A>C COCA-CN 22 41536237 41536237 single base substitution C T synonymous_variant D618D 1854C>T COCA-CN 22 41542800 41542800 single base substitution C T missense_variant P704L 2111C>T COCA-CN 22 41542839 41542839 single base substitution T G intron_variant COCA-CN 22 41543721 41543721 single base substitution G A intron_variant COCA-CN 22 41543755 41543755 single base substitution G A intron_variant COCA-CN 22 41543985 41543985 single base substitution T G intron_variant COCA-CN 22 41545292 41545292 single base substitution T A intron_variant COCA-CN 22 41548193 41548193 single base substitution C A intron_variant COCA-CN 22 41548203 41548203 single base substitution C A splice_region_variant COCA-CN 22 41548310 41548310 single base substitution C T missense_variant S1033L 3098C>T COCA-CN 22 41551242 41551242 single base substitution T C intron_variant COCA-CN 22 41556756 41556756 single base substitution T G intron_variant COCA-CN 22 41559950 41559950 single base substitution C A intron_variant COCA-CN 22 41572900 41572900 single base substitution G A missense_variant D1729N 5185G>A COCA-CN 22 41573201 41573201 single base substitution G A missense_variant R1829H 5486G>A COCA-CN 22 41574620 41574620 single base substitution C A missense_variant S2302Y 6905C>A EOPC-DE 22 41529699 41529699 single base substitution C T intron_variant EOPC-DE 22 41554311 41554311 single base substitution A G intron_variant ESAD-UK 22 41484468 41484468 single base substitution C T upstream_gene_variant ESAD-UK 22 41485998 41485998 single base substitution C T upstream_gene_variant ESAD-UK 22 41487564 41487564 single base substitution G C upstream_gene_variant ESAD-UK 22 41491147 41491147 single base substitution T C intron_variant ESAD-UK 22 41491776 41491776 single base substitution A T intron_variant ESAD-UK 22 41493998 41493998 deletion of <=200bp A - intron_variant ESAD-UK 22 41498452 41498452 single base substitution T C intron_variant ESAD-UK 22 41498541 41498541 single base substitution G A intron_variant ESAD-UK 22 41500300 41500300 single base substitution G T intron_variant ESAD-UK 22 41506065 41506065 deletion of <=200bp G - intron_variant ESAD-UK 22 41508716 41508716 insertion of <=200bp - TG intron_variant ESAD-UK 22 41509004 41509004 single base substitution T A intron_variant ESAD-UK 22 41514926 41514926 single base substitution T G intron_variant ESAD-UK 22 41518005 41518005 deletion of <=200bp A - intron_variant ESAD-UK 22 41518120 41518120 single base substitution A C intron_variant ESAD-UK 22 41518419 41518419 single base substitution C T intron_variant ESAD-UK 22 41519792 41519792 single base substitution G T intron_variant ESAD-UK 22 41521374 41521374 single base substitution G A intron_variant ESAD-UK 22 41522815 41522815 single base substitution C T intron_variant ESAD-UK 22 41523495 41523495 single base substitution A G missense_variant Q304R 911A>G ESAD-UK 22 41525139 41525139 single base substitution C T intron_variant ESAD-UK 22 41526439 41526440 deletion of <=200bp GA - intron_variant ESAD-UK 22 41527186 41527186 single base substitution C G intron_variant ESAD-UK 22 41534104 41534104 single base substitution C G intron_variant ESAD-UK 22 41534940 41534940 single base substitution T A intron_variant ESAD-UK 22 41537034 41537034 single base substitution A C intron_variant ESAD-UK 22 41538056 41538056 single base substitution A C intron_variant ESAD-UK 22 41542228 41542228 single base substitution G A intron_variant ESAD-UK 22 41542479 41542479 single base substitution C T intron_variant ESAD-UK 22 41544412 41544412 single base substitution T G intron_variant ESAD-UK 22 41545790 41545790 single base substitution C T missense_variant P802L 2405C>T ESAD-UK 22 41546715 41546715 single base substitution A G intron_variant ESAD-UK 22 41548953 41548953 single base substitution G A intron_variant ESAD-UK 22 41550787 41550787 single base substitution T A intron_variant ESAD-UK 22 41550789 41550789 single base substitution A T intron_variant ESAD-UK 22 41552077 41552077 single base substitution G A intron_variant ESAD-UK 22 41553025 41553025 single base substitution G A intron_variant ESAD-UK 22 41554094 41554094 single base substitution C G intron_variant ESAD-UK 22 41555053 41555053 single base substitution G A intron_variant ESAD-UK 22 41556537 41556537 single base substitution T G intron_variant ESAD-UK 22 41556608 41556608 single base substitution C G intron_variant ESAD-UK 22 41557536 41557536 single base substitution G C intron_variant ESAD-UK 22 41558162 41558162 single base substitution G C intron_variant ESAD-UK 22 41559872 41559872 single base substitution C T intron_variant ESAD-UK 22 41561764 41561764 single base substitution G A intron_variant ESAD-UK 22 41564852 41564852 single base substitution T C missense_variant C1385R 4153T>C ESAD-UK 22 41567153 41567153 single base substitution T C intron_variant ESAD-UK 22 41568114 41568114 single base substitution T G intron_variant ESAD-UK 22 41575031 41575031 deletion of <=200bp T - 3_prime_UTR_variant ESAD-UK 22 41579774 41579774 single base substitution G C downstream_gene_variant ESCA-CN 22 41537138 41537138 single base substitution G C missense_variant Q655H 1965G>C ESCA-CN 22 41546128 41546128 single base substitution C T missense_variant R915C 2743C>T ESCA-CN 22 41564775 41564775 single base substitution C T missense_variant A1359V 4076C>T ESCA-CN 22 41565529 41565529 single base substitution G A missense_variant D1399N 4195G>A ESCA-CN 22 41565529 41565529 single base substitution G T missense_variant D1399Y 4195G>T ESCA-CN 22 41566478 41566478 single base substitution C T missense_variant P1452L 4355C>T ESCA-CN 22 41568569 41568569 single base substitution G A missense_variant D1507N 4519G>A ESCA-CN 22 41568626 41568626 single base substitution G A missense_variant E1526K 4576G>A ESCA-CN 22 41568668 41568668 single base substitution G A splice_donor_variant ESCA-CN 22 41572338 41572338 single base substitution C T synonymous_variant L1623L 4867C>T GBM-US 22 41556657 41556657 single base substitution G A missense_variant C1201Y 3602G>A GBM-US 22 41564740 41564740 single base substitution A G synonymous_variant G1347G 4041A>G GBM-US 22 41564810 41564810 single base substitution C T synonymous_variant L1371L 4111C>T KIRC-US 22 41513594 41513594 single base substitution C A missense_variant N166K 498C>A KIRC-US 22 41536219 41536219 single base substitution T C synonymous_variant A612A 1836T>C KIRC-US 22 41572994 41572994 single base substitution A G missense_variant K1760R 5279A>G KIRC-US 22 41573737 41573737 single base substitution T C missense_variant S2008P 6022T>C KIRC-US 22 41574358 41574358 single base substitution C A missense_variant Q2215K 6643C>A KIRC-US 22 41574794 41574794 single base substitution A G missense_variant E2360G 7079A>G KIRP-US 22 41489069 41489069 single base substitution C G missense_variant P21A 61C>G KIRP-US 22 41558757 41558757 deletion of <=200bp A - frameshift_variant R1234 KIRP-US 22 41574164 41574176 deletion of <=200bp CACAGCAGCAACT - frameshift_variant PQQQL2150 LAML-KR 22 41485792 41485792 single base substitution A G upstream_gene_variant LAML-KR 22 41501110 41501110 single base substitution A G intron_variant LAML-KR 22 41508169 41508169 single base substitution A G intron_variant LAML-KR 22 41515183 41515183 single base substitution T A intron_variant LAML-KR 22 41515187 41515187 single base substitution T A intron_variant LAML-KR 22 41537689 41537689 single base substitution C T intron_variant LAML-KR 22 41545292 41545292 single base substitution T A intron_variant LAML-KR 22 41553414 41553414 single base substitution T A splice_donor_variant LAML-KR 22 41554534 41554534 single base substitution C A intron_variant LAML-KR 22 41556419 41556419 single base substitution A T intron_variant LAML-KR 22 41559422 41559422 single base substitution G C intron_variant LAML-KR 22 41559440 41559440 single base substitution A G intron_variant LAML-KR 22 41569502 41569502 single base substitution C G intron_variant LGG-US 22 41566476 41566476 single base substitution T C synonymous_variant H1451H 4353T>C LICA-CN 22 41548264 41548264 single base substitution G T stop_gained E1018* 3052G>T LICA-CN 22 41551069 41551069 single base substitution A C missense_variant E1071D 3213A>C LICA-FR 22 41491553 41491553 insertion of <=200bp - T intron_variant LICA-FR 22 41498034 41498034 insertion of <=200bp - T intron_variant LICA-FR 22 41515184 41515184 single base substitution T A intron_variant LICA-FR 22 41515187 41515187 single base substitution T A intron_variant LICA-FR 22 41525894 41525894 single base substitution T G missense_variant V390G 1169T>G LICA-FR 22 41527510 41527510 single base substitution C G synonymous_variant A467A 1401C>G LICA-FR 22 41542798 41542798 single base substitution G A missense_variant M703I 2109G>A LICA-FR 22 41573353 41573353 single base substitution C A missense_variant P1880T 5638C>A LICA-FR 22 41573938 41573938 single base substitution C A missense_variant H2075N 6223C>A LICA-FR 22 41578139 41578139 single base substitution T C downstream_gene_variant LICA-FR 22 41578740 41578740 insertion of <=200bp - A downstream_gene_variant LIHC-US 22 41545854 41545854 single base substitution T C synonymous_variant P823P 2469T>C LIHC-US 22 41560092 41560092 single base substitution A T missense_variant H1255L 3764A>T LIHC-US 22 41569690 41569690 single base substitution A G missense_variant S1561G 4681A>G LIHC-US 22 41573037 41573037 single base substitution A T missense_variant K1774N 5322A>T LIHC-US 22 41574846 41574846 single base substitution T C synonymous_variant A2377A 7131T>C LINC-JP 22 41484931 41484931 single base substitution T C upstream_gene_variant LINC-JP 22 41486844 41486844 single base substitution T G upstream_gene_variant LINC-JP 22 41486875 41486875 deletion of <=200bp A - upstream_gene_variant LINC-JP 22 41488842 41488842 single base substitution T C 5_prime_UTR_variant LINC-JP 22 41489202 41489202 single base substitution C T intron_variant LINC-JP 22 41492232 41492232 single base substitution A G intron_variant LINC-JP 22 41501532 41501532 single base substitution A G intron_variant LINC-JP 22 41513861 41513861 single base substitution T A intron_variant LINC-JP 22 41522236 41522236 single base substitution G C intron_variant LINC-JP 22 41525013 41525013 single base substitution A G intron_variant LINC-JP 22 41531207 41531207 single base substitution A T intron_variant LINC-JP 22 41533580 41533580 single base substitution A G intron_variant LINC-JP 22 41536286 41536286 insertion of <=200bp - AA intron_variant LINC-JP 22 41540384 41540384 single base substitution G A intron_variant LINC-JP 22 41543315 41543315 single base substitution A C intron_variant LINC-JP 22 41548329 41548329 single base substitution G A synonymous_variant P1039P 3117G>A LINC-JP 22 41550262 41550262 single base substitution A G intron_variant LINC-JP 22 41551331 41551331 single base substitution C T intron_variant LINC-JP 22 41554269 41554269 single base substitution A T intron_variant LINC-JP 22 41556893 41556893 single base substitution G T intron_variant LINC-JP 22 41559958 41559958 single base substitution A G intron_variant LINC-JP 22 41563806 41563808 deletion of <=200bp CTG - intron_variant LINC-JP 22 41568688 41568688 single base substitution T G intron_variant LINC-JP 22 41572331 41572341 deletion of <=200bp CTGCGATCTGA - frameshift_variant PCDLM1620 LINC-JP 22 41572578 41572591 deletion of <=200bp GTTCTGAGGGGCCA - intron_variant LIRI-JP 22 41483158 41483158 single base substitution G A upstream_gene_variant LIRI-JP 22 41488600 41488602 deletion of <=200bp AGG - 5_prime_UTR_variant LIRI-JP 22 41491831 41491831 single base substitution G A intron_variant LIRI-JP 22 41492742 41492742 single base substitution C T intron_variant LIRI-JP 22 41492914 41492914 single base substitution T C intron_variant LIRI-JP 22 41493334 41493334 single base substitution A G intron_variant LIRI-JP 22 41493401 41493401 single base substitution C A intron_variant LIRI-JP 22 41493624 41493624 single base substitution G A intron_variant LIRI-JP 22 41494603 41494603 single base substitution C T intron_variant LIRI-JP 22 41494895 41494895 single base substitution A G intron_variant LIRI-JP 22 41494920 41494920 single base substitution G A intron_variant LIRI-JP 22 41498261 41498261 single base substitution C T intron_variant LIRI-JP 22 41501391 41501391 deletion of <=200bp G - intron_variant LIRI-JP 22 41501565 41501565 single base substitution G C intron_variant LIRI-JP 22 41503252 41503252 single base substitution A C intron_variant LIRI-JP 22 41510738 41510738 single base substitution G A intron_variant LIRI-JP 22 41511553 41511553 single base substitution T A intron_variant LIRI-JP 22 41512320 41512320 single base substitution A G intron_variant LIRI-JP 22 41513049 41513049 single base substitution A T intron_variant LIRI-JP 22 41516087 41516087 single base substitution C G intron_variant LIRI-JP 22 41516818 41516818 single base substitution G A intron_variant LIRI-JP 22 41516819 41516819 single base substitution C G intron_variant LIRI-JP 22 41522818 41522818 single base substitution G A intron_variant LIRI-JP 22 41525421 41525421 single base substitution C T intron_variant LIRI-JP 22 41527129 41527129 single base substitution C T intron_variant LIRI-JP 22 41527192 41527192 single base substitution C T intron_variant LIRI-JP 22 41527412 41527412 single base substitution G A missense_variant V435I 1303G>A LIRI-JP 22 41527794 41527794 single base substitution A G intron_variant LIRI-JP 22 41529637 41529637 single base substitution G T intron_variant LIRI-JP 22 41530886 41530886 single base substitution G T intron_variant LIRI-JP 22 41540126 41540126 single base substitution T A intron_variant LIRI-JP 22 41541051 41541051 single base substitution C T intron_variant LIRI-JP 22 41542524 41542524 single base substitution A G intron_variant LIRI-JP 22 41543217 41543217 single base substitution G T intron_variant LIRI-JP 22 41543758 41543758 single base substitution A G intron_variant LIRI-JP 22 41544052 41544052 single base substitution A G intron_variant LIRI-JP 22 41547881 41547881 single base substitution T G synonymous_variant P954P 2862T>G LIRI-JP 22 41547893 41547893 single base substitution T C synonymous_variant S958S 2874T>C LIRI-JP 22 41548047 41548047 single base substitution G C intron_variant LIRI-JP 22 41548286 41548286 single base substitution A G missense_variant E1025G 3074A>G LIRI-JP 22 41549256 41549275 deletion of <=200bp CTAGTGATCTGCAAAAGGCA - intron_variant LIRI-JP 22 41552560 41552560 single base substitution A G intron_variant LIRI-JP 22 41553192 41553192 single base substitution A G missense_variant K1094R 3281A>G LIRI-JP 22 41553302 41553302 single base substitution T A missense_variant Y1131N 3391T>A LIRI-JP 22 41554772 41554772 insertion of <=200bp - T intron_variant LIRI-JP 22 41555129 41555129 single base substitution A G intron_variant LIRI-JP 22 41555439 41555439 single base substitution T C intron_variant LIRI-JP 22 41557515 41557515 single base substitution G A intron_variant LIRI-JP 22 41558363 41558363 single base substitution A C intron_variant LIRI-JP 22 41558787 41558787 single base substitution A C splice_region_variant LIRI-JP 22 41561957 41561957 single base substitution T G intron_variant LIRI-JP 22 41562470 41562470 single base substitution A G intron_variant LIRI-JP 22 41562835 41562835 single base substitution A C intron_variant LIRI-JP 22 41564119 41564119 single base substitution C T intron_variant LIRI-JP 22 41566424 41566424 single base substitution A G missense_variant H1434R 4301A>G LIRI-JP 22 41566650 41566650 single base substitution C T intron_variant LIRI-JP 22 41568668 41568668 single base substitution G A splice_donor_variant LIRI-JP 22 41569577 41569577 single base substitution A G intron_variant LIRI-JP 22 41574503 41574503 single base substitution G A missense_variant R2263Q 6788G>A LIRI-JP 22 41574637 41574637 single base substitution C T missense_variant R2308C 6922C>T LUSC-KR 22 41483249 41483249 single base substitution C T upstream_gene_variant LUSC-KR 22 41483803 41483803 single base substitution G A upstream_gene_variant LUSC-KR 22 41486530 41486530 single base substitution G A upstream_gene_variant LUSC-KR 22 41487763 41487763 single base substitution G T upstream_gene_variant LUSC-KR 22 41491523 41491523 single base substitution G T intron_variant LUSC-KR 22 41492658 41492658 single base substitution C T intron_variant LUSC-KR 22 41497270 41497270 single base substitution G T intron_variant LUSC-KR 22 41500623 41500623 single base substitution C T intron_variant LUSC-KR 22 41502280 41502280 single base substitution C G intron_variant LUSC-KR 22 41504878 41504878 single base substitution G T intron_variant LUSC-KR 22 41509017 41509017 single base substitution G T intron_variant LUSC-KR 22 41515183 41515183 single base substitution T A intron_variant LUSC-KR 22 41515184 41515184 single base substitution T A intron_variant LUSC-KR 22 41515186 41515186 single base substitution T A intron_variant LUSC-KR 22 41515190 41515190 single base substitution T A intron_variant LUSC-KR 22 41516314 41516314 single base substitution C T intron_variant LUSC-KR 22 41522066 41522066 single base substitution A T intron_variant LUSC-KR 22 41527796 41527796 single base substitution G T intron_variant LUSC-KR 22 41533105 41533105 single base substitution G A intron_variant LUSC-KR 22 41535324 41535324 single base substitution G T intron_variant LUSC-KR 22 41535523 41535523 single base substitution C T intron_variant LUSC-KR 22 41538150 41538150 single base substitution C T intron_variant LUSC-KR 22 41539646 41539646 single base substitution C T intron_variant LUSC-KR 22 41540831 41540831 single base substitution C T intron_variant LUSC-KR 22 41542605 41542605 single base substitution C T intron_variant LUSC-KR 22 41544484 41544484 single base substitution C G intron_variant LUSC-KR 22 41545561 41545561 single base substitution G C intron_variant LUSC-KR 22 41547849 41547849 single base substitution G T missense_variant A944S 2830G>T LUSC-KR 22 41548008 41548008 single base substitution A G missense_variant I997V 2989A>G LUSC-KR 22 41554424 41554424 single base substitution C T synonymous_variant F1170F 3510C>T LUSC-KR 22 41554789 41554789 single base substitution C T intron_variant LUSC-KR 22 41555006 41555006 single base substitution C G intron_variant LUSC-KR 22 41555470 41555470 single base substitution C T intron_variant LUSC-KR 22 41555640 41555640 single base substitution C G intron_variant LUSC-KR 22 41556254 41556254 single base substitution C T intron_variant LUSC-KR 22 41556279 41556279 single base substitution C G intron_variant LUSC-KR 22 41556389 41556389 single base substitution C T intron_variant LUSC-KR 22 41556655 41556655 single base substitution C T synonymous_variant F1200F 3600C>T LUSC-KR 22 41556722 41556722 single base substitution C G missense_variant Q1223E 3667C>G LUSC-KR 22 41556887 41556887 single base substitution C T intron_variant LUSC-KR 22 41557172 41557172 single base substitution C G intron_variant LUSC-KR 22 41557371 41557371 single base substitution C T intron_variant LUSC-KR 22 41557614 41557614 single base substitution C T intron_variant LUSC-KR 22 41557620 41557620 single base substitution C A intron_variant LUSC-KR 22 41557749 41557749 single base substitution C G intron_variant LUSC-KR 22 41558109 41558109 single base substitution C T intron_variant LUSC-KR 22 41558216 41558216 single base substitution C T intron_variant LUSC-KR 22 41559652 41559652 single base substitution G A intron_variant LUSC-KR 22 41560142 41560142 single base substitution T G splice_region_variant LUSC-KR 22 41563819 41563819 single base substitution T G intron_variant LUSC-KR 22 41563823 41563823 single base substitution T G intron_variant LUSC-KR 22 41564240 41564240 single base substitution A G intron_variant LUSC-KR 22 41564287 41564287 single base substitution T C intron_variant LUSC-KR 22 41566595 41566595 single base substitution C T intron_variant LUSC-KR 22 41568480 41568480 single base substitution T C intron_variant LUSC-KR 22 41569609 41569609 single base substitution C T intron_variant LUSC-KR 22 41569887 41569887 single base substitution G A intron_variant LUSC-US 22 41521907 41521907 single base substitution T G missense_variant Y257D 769T>G LUSC-US 22 41565505 41565505 single base substitution A G splice_acceptor_variant LUSC-US 22 41565527 41565527 single base substitution T C missense_variant L1398P 4193T>C LUSC-US 22 41565529 41565529 single base substitution G A missense_variant D1399N 4195G>A LUSC-US 22 41565575 41565575 single base substitution A G missense_variant Y1414C 4241A>G LUSC-US 22 41572364 41572364 single base substitution C T synonymous_variant L1631L 4893C>T LUSC-US 22 41573348 41573348 single base substitution C A missense_variant T1878N 5633C>A LUSC-US 22 41574082 41574082 single base substitution G T missense_variant G2123W 6367G>T LUSC-US 22 41574090 41574090 single base substitution C A missense_variant H2125Q 6375C>A LUSC-US 22 41574204 41574204 single base substitution C T synonymous_variant P2163P 6489C>T MALY-DE 22 41487474 41487474 single base substitution C G upstream_gene_variant MALY-DE 22 41494067 41494067 single base substitution T G intron_variant MALY-DE 22 41496645 41496648 deletion of <=200bp TATT - intron_variant MALY-DE 22 41500983 41500983 insertion of <=200bp - A intron_variant MALY-DE 22 41504985 41504985 single base substitution T G intron_variant MALY-DE 22 41535465 41535465 single base substitution T C intron_variant MALY-DE 22 41538594 41538594 single base substitution A T intron_variant MALY-DE 22 41550419 41550419 single base substitution T G intron_variant MALY-DE 22 41551610 41551610 deletion of <=200bp T - intron_variant MALY-DE 22 41555163 41555163 single base substitution T C intron_variant MALY-DE 22 41556193 41556193 single base substitution T A intron_variant MALY-DE 22 41556203 41556203 single base substitution T C intron_variant MALY-DE 22 41556674 41556674 single base substitution G T stop_gained E1207* 3619G>T MALY-DE 22 41565562 41565562 single base substitution A T missense_variant R1410W 4228A>T MALY-DE 22 41566435 41566435 single base substitution T C missense_variant C1438R 4312T>C MALY-DE 22 41566522 41566522 single base substitution T G missense_variant Y1467D 4399T>G MALY-DE 22 41579668 41579668 deletion of <=200bp T - downstream_gene_variant MELA-AU 22 41482867 41482867 single base substitution G A upstream_gene_variant MELA-AU 22 41483015 41483015 single base substitution G A upstream_gene_variant MELA-AU 22 41483512 41483512 single base substitution G A upstream_gene_variant MELA-AU 22 41483539 41483539 single base substitution G A upstream_gene_variant MELA-AU 22 41483802 41483802 single base substitution C T upstream_gene_variant MELA-AU 22 41484046 41484046 single base substitution C T upstream_gene_variant MELA-AU 22 41484085 41484085 single base substitution G A upstream_gene_variant MELA-AU 22 41484557 41484557 single base substitution G A upstream_gene_variant MELA-AU 22 41484726 41484726 single base substitution G A upstream_gene_variant MELA-AU 22 41484878 41484878 single base substitution G A upstream_gene_variant MELA-AU 22 41485102 41485102 single base substitution C T upstream_gene_variant MELA-AU 22 41485472 41485472 single base substitution C T upstream_gene_variant MELA-AU 22 41486071 41486071 single base substitution C T upstream_gene_variant MELA-AU 22 41486653 41486653 single base substitution G A upstream_gene_variant MELA-AU 22 41486892 41486892 single base substitution A C upstream_gene_variant MELA-AU 22 41487114 41487114 single base substitution G A upstream_gene_variant MELA-AU 22 41487584 41487584 single base substitution G A upstream_gene_variant MELA-AU 22 41487696 41487696 single base substitution C T upstream_gene_variant MELA-AU 22 41487881 41487881 single base substitution G A 5_prime_UTR_variant MELA-AU 22 41487952 41487952 single base substitution G A 5_prime_UTR_variant MELA-AU 22 41488972 41488972 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 22 41489083 41489083 single base substitution G A synonymous_variant A25A 75G>A MELA-AU 22 41489479 41489479 single base substitution C T intron_variant MELA-AU 22 41489486 41489486 single base substitution C T intron_variant MELA-AU 22 41490021 41490021 single base substitution C T intron_variant MELA-AU 22 41490094 41490094 single base substitution C T intron_variant MELA-AU 22 41492830 41492830 single base substitution C T intron_variant MELA-AU 22 41493907 41493907 single base substitution C T intron_variant MELA-AU 22 41494157 41494157 single base substitution C T intron_variant MELA-AU 22 41494417 41494417 single base substitution C G intron_variant MELA-AU 22 41494835 41494835 single base substitution C T intron_variant MELA-AU 22 41495377 41495377 single base substitution C T intron_variant MELA-AU 22 41495691 41495691 single base substitution C T intron_variant MELA-AU 22 41496038 41496038 single base substitution T C intron_variant MELA-AU 22 41497173 41497173 single base substitution G A intron_variant MELA-AU 22 41497232 41497232 single base substitution C T intron_variant MELA-AU 22 41497320 41497320 single base substitution C T intron_variant MELA-AU 22 41497526 41497526 single base substitution C T intron_variant MELA-AU 22 41497986 41497986 insertion of <=200bp - A intron_variant MELA-AU 22 41500897 41500898 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 22 41501022 41501022 deletion of <=200bp A - intron_variant MELA-AU 22 41501717 41501717 single base substitution G A intron_variant MELA-AU 22 41501720 41501720 single base substitution T A intron_variant MELA-AU 22 41502953 41502953 single base substitution C T intron_variant MELA-AU 22 41503423 41503423 single base substitution A C intron_variant MELA-AU 22 41503509 41503509 single base substitution A G intron_variant MELA-AU 22 41504511 41504511 single base substitution C T intron_variant MELA-AU 22 41504959 41504959 single base substitution G A intron_variant MELA-AU 22 41506455 41506455 single base substitution C T intron_variant MELA-AU 22 41506713 41506713 single base substitution T C intron_variant MELA-AU 22 41506966 41506966 single base substitution T A intron_variant MELA-AU 22 41506967 41506967 single base substitution T A intron_variant MELA-AU 22 41507199 41507246 deletion of <=200bp TAAACTCCTGACCTCCAGCAGTCCACCTGTCTCAGCCTCCCAAAGTGC - intron_variant MELA-AU 22 41507426 41507426 single base substitution T C intron_variant MELA-AU 22 41507548 41507548 single base substitution C T intron_variant MELA-AU 22 41508048 41508048 single base substitution C T intron_variant MELA-AU 22 41508529 41508529 single base substitution C T intron_variant MELA-AU 22 41508683 41508683 single base substitution C T intron_variant MELA-AU 22 41508713 41508713 single base substitution G A intron_variant MELA-AU 22 41509422 41509422 single base substitution C T intron_variant MELA-AU 22 41509914 41509914 single base substitution C T intron_variant MELA-AU 22 41510802 41510802 single base substitution A C intron_variant MELA-AU 22 41510852 41510852 single base substitution G A intron_variant MELA-AU 22 41511595 41511595 single base substitution C T intron_variant MELA-AU 22 41512088 41512088 single base substitution C T intron_variant MELA-AU 22 41512145 41512145 single base substitution G T intron_variant MELA-AU 22 41512641 41512641 single base substitution C T intron_variant MELA-AU 22 41513349 41513349 single base substitution C T synonymous_variant L85L 253C>T MELA-AU 22 41514252 41514252 single base substitution C T intron_variant MELA-AU 22 41514435 41514435 single base substitution C T intron_variant MELA-AU 22 41514539 41514539 single base substitution C T intron_variant MELA-AU 22 41514818 41514818 single base substitution C T intron_variant MELA-AU 22 41515129 41515129 single base substitution C T intron_variant MELA-AU 22 41515284 41515284 single base substitution C T intron_variant MELA-AU 22 41515819 41515819 single base substitution C T intron_variant MELA-AU 22 41516903 41516903 single base substitution G C intron_variant MELA-AU 22 41517238 41517238 single base substitution C T intron_variant MELA-AU 22 41517624 41517624 single base substitution T C intron_variant MELA-AU 22 41518799 41518799 single base substitution C T intron_variant MELA-AU 22 41519088 41519089 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 22 41519180 41519181 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 22 41519974 41519974 single base substitution C T intron_variant MELA-AU 22 41521450 41521450 single base substitution G A intron_variant MELA-AU 22 41521477 41521477 single base substitution C T intron_variant MELA-AU 22 41521995 41521995 single base substitution C T missense_variant P286L 857C>T MELA-AU 22 41522149 41522149 single base substitution T C intron_variant MELA-AU 22 41522408 41522408 single base substitution T G intron_variant MELA-AU 22 41523060 41523060 single base substitution T C intron_variant MELA-AU 22 41523115 41523115 single base substitution C T intron_variant MELA-AU 22 41523662 41523662 single base substitution G A missense_variant E360K 1078G>A MELA-AU 22 41524096 41524096 single base substitution G T intron_variant MELA-AU 22 41525966 41525966 single base substitution G T missense_variant C414F 1241G>T MELA-AU 22 41526130 41526130 single base substitution T A intron_variant MELA-AU 22 41527509 41527509 single base substitution C T missense_variant A467V 1400C>T MELA-AU 22 41527579 41527579 single base substitution C T synonymous_variant N490N 1470C>T MELA-AU 22 41527608 41527608 single base substitution C T missense_variant P500L 1499C>T MELA-AU 22 41528724 41528724 single base substitution C T intron_variant MELA-AU 22 41529112 41529112 single base substitution T G intron_variant MELA-AU 22 41529117 41529117 single base substitution G A intron_variant MELA-AU 22 41529278 41529278 single base substitution C T intron_variant MELA-AU 22 41529355 41529355 single base substitution A T intron_variant MELA-AU 22 41530432 41530432 single base substitution C T intron_variant MELA-AU 22 41531361 41531361 single base substitution C T intron_variant MELA-AU 22 41531555 41531555 single base substitution C T intron_variant MELA-AU 22 41531681 41531681 single base substitution G A intron_variant MELA-AU 22 41531996 41531996 single base substitution C T intron_variant MELA-AU 22 41532717 41532717 single base substitution C T intron_variant MELA-AU 22 41533570 41533570 single base substitution C T intron_variant MELA-AU 22 41533645 41533645 single base substitution C T intron_variant MELA-AU 22 41533858 41533858 single base substitution C T intron_variant MELA-AU 22 41533962 41533962 single base substitution C T intron_variant MELA-AU 22 41534791 41534791 single base substitution T A intron_variant MELA-AU 22 41534799 41534799 single base substitution C T intron_variant MELA-AU 22 41535042 41535043 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 22 41535077 41535077 single base substitution C T intron_variant MELA-AU 22 41535356 41535356 single base substitution T C intron_variant MELA-AU 22 41536051 41536051 single base substitution T A intron_variant MELA-AU 22 41536447 41536447 single base substitution T C intron_variant MELA-AU 22 41537005 41537005 single base substitution G C intron_variant MELA-AU 22 41537008 41537008 single base substitution C T intron_variant MELA-AU 22 41537618 41537618 single base substitution T C intron_variant MELA-AU 22 41537806 41537806 single base substitution G T intron_variant MELA-AU 22 41537969 41537969 single base substitution C T intron_variant MELA-AU 22 41538654 41538654 single base substitution C T intron_variant MELA-AU 22 41539552 41539552 single base substitution C T intron_variant MELA-AU 22 41540612 41540612 single base substitution C T intron_variant MELA-AU 22 41541764 41541765 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 22 41542278 41542278 single base substitution C T intron_variant MELA-AU 22 41543422 41543422 single base substitution A G intron_variant MELA-AU 22 41543625 41543625 single base substitution C T intron_variant MELA-AU 22 41543933 41543933 single base substitution C T missense_variant P742S 2224C>T MELA-AU 22 41544006 41544006 single base substitution C T intron_variant MELA-AU 22 41544206 41544206 single base substitution C T intron_variant MELA-AU 22 41544322 41544322 single base substitution C T intron_variant MELA-AU 22 41545168 41545168 single base substitution C T missense_variant P790S 2368C>T MELA-AU 22 41546200 41546200 single base substitution C T missense_variant P939S 2815C>T MELA-AU 22 41546383 41546383 single base substitution C T intron_variant MELA-AU 22 41547164 41547164 single base substitution C T intron_variant MELA-AU 22 41547172 41547172 single base substitution C T intron_variant MELA-AU 22 41547756 41547756 single base substitution C T intron_variant MELA-AU 22 41548102 41548102 single base substitution T C intron_variant MELA-AU 22 41548627 41548627 single base substitution C T intron_variant MELA-AU 22 41548960 41548960 single base substitution C T intron_variant MELA-AU 22 41549857 41549857 single base substitution G A intron_variant MELA-AU 22 41550193 41550193 single base substitution C T intron_variant MELA-AU 22 41550547 41550547 single base substitution A T intron_variant MELA-AU 22 41551054 41551054 single base substitution C T synonymous_variant Y1066Y 3198C>T MELA-AU 22 41551784 41551784 single base substitution C T intron_variant MELA-AU 22 41551950 41551950 single base substitution C T intron_variant MELA-AU 22 41552104 41552104 single base substitution C T intron_variant MELA-AU 22 41552137 41552137 single base substitution C T intron_variant MELA-AU 22 41552226 41552226 single base substitution A G intron_variant MELA-AU 22 41552981 41552981 single base substitution C T intron_variant MELA-AU 22 41553355 41553355 single base substitution C G synonymous_variant V1148V 3444C>G MELA-AU 22 41554874 41554874 single base substitution C T intron_variant MELA-AU 22 41554947 41554947 single base substitution T C intron_variant MELA-AU 22 41556142 41556142 single base substitution C T intron_variant MELA-AU 22 41556145 41556145 single base substitution C T intron_variant MELA-AU 22 41556435 41556435 single base substitution C A intron_variant MELA-AU 22 41556473 41556473 single base substitution C T intron_variant MELA-AU 22 41556542 41556542 single base substitution C T intron_variant MELA-AU 22 41556685 41556685 single base substitution G A synonymous_variant G1210G 3630G>A MELA-AU 22 41557423 41557423 single base substitution C T intron_variant MELA-AU 22 41557935 41557935 single base substitution G A intron_variant MELA-AU 22 41558043 41558043 single base substitution C A intron_variant MELA-AU 22 41560220 41560220 single base substitution T C intron_variant MELA-AU 22 41560465 41560465 single base substitution C T intron_variant MELA-AU 22 41560480 41560480 single base substitution C T intron_variant MELA-AU 22 41562079 41562080 multiple base substitution (>=2bp and <=200bp) AC TT intron_variant MELA-AU 22 41563868 41563868 single base substitution C T intron_variant MELA-AU 22 41564274 41564274 single base substitution C T intron_variant MELA-AU 22 41564352 41564352 single base substitution C T intron_variant MELA-AU 22 41565409 41565409 single base substitution C T intron_variant MELA-AU 22 41566012 41566012 single base substitution C T intron_variant MELA-AU 22 41566126 41566126 single base substitution G A intron_variant MELA-AU 22 41566327 41566327 single base substitution C T intron_variant MELA-AU 22 41566739 41566739 single base substitution C G intron_variant MELA-AU 22 41567815 41567815 single base substitution C T intron_variant MELA-AU 22 41568475 41568475 single base substitution T C intron_variant MELA-AU 22 41568648 41568648 single base substitution C A missense_variant T1533N 4598C>A MELA-AU 22 41568685 41568686 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 22 41569287 41569287 single base substitution T C intron_variant MELA-AU 22 41569340 41569341 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 22 41569878 41569878 single base substitution G A intron_variant MELA-AU 22 41570298 41570299 multiple base substitution (>=2bp and <=200bp) GG CT intron_variant MELA-AU 22 41570415 41570415 insertion of <=200bp - A intron_variant MELA-AU 22 41570625 41570625 single base substitution A T intron_variant MELA-AU 22 41571506 41571506 single base substitution C T intron_variant MELA-AU 22 41572147 41572147 single base substitution C T intron_variant MELA-AU 22 41572540 41572540 single base substitution C T splice_region_variant MELA-AU 22 41572568 41572568 single base substitution C T intron_variant MELA-AU 22 41573263 41573263 single base substitution C T missense_variant P1850S 5548C>T MELA-AU 22 41573896 41573897 multiple base substitution (>=2bp and <=200bp) CC TT missense_variant P2061F 6181CC>TT MELA-AU 22 41574631 41574631 single base substitution C T stop_gained Q2306* 6916C>T MELA-AU 22 41576835 41576835 single base substitution C T downstream_gene_variant MELA-AU 22 41577396 41577396 single base substitution C G downstream_gene_variant MELA-AU 22 41577794 41577794 single base substitution A G downstream_gene_variant MELA-AU 22 41577812 41577812 single base substitution C T downstream_gene_variant MELA-AU 22 41578103 41578103 single base substitution G C downstream_gene_variant MELA-AU 22 41578473 41578473 single base substitution G A downstream_gene_variant MELA-AU 22 41578792 41578792 single base substitution G T downstream_gene_variant MELA-AU 22 41579697 41579697 single base substitution C T downstream_gene_variant MELA-AU 22 41580725 41580725 single base substitution A T downstream_gene_variant NBL-US 22 41546128 41546128 single base substitution C T missense_variant R915C 2743C>T ORCA-IN 22 41484015 41484016 deletion of <=200bp AG - upstream_gene_variant ORCA-IN 22 41493403 41493403 single base substitution T C intron_variant ORCA-IN 22 41513607 41513607 single base substitution G T missense_variant A171S 511G>T ORCA-IN 22 41533693 41533693 single base substitution G A synonymous_variant L553L 1659G>A ORCA-IN 22 41556657 41556657 single base substitution G A missense_variant C1201Y 3602G>A ORCA-IN 22 41565529 41565529 single base substitution G A missense_variant D1399N 4195G>A ORCA-IN 22 41565529 41565529 single base substitution G T missense_variant D1399Y 4195G>T ORCA-IN 22 41574571 41574571 single base substitution C A missense_variant P2286T 6856C>A OV-AU 22 41483622 41483622 single base substitution A C upstream_gene_variant OV-AU 22 41490678 41490678 single base substitution G A intron_variant OV-AU 22 41501133 41501133 single base substitution G A intron_variant OV-AU 22 41502568 41502568 single base substitution G A intron_variant OV-AU 22 41515359 41515359 single base substitution T C intron_variant OV-AU 22 41530217 41530217 single base substitution G A intron_variant OV-AU 22 41531599 41531599 single base substitution T C intron_variant OV-AU 22 41535162 41535162 single base substitution T C intron_variant OV-AU 22 41538097 41538097 single base substitution T C intron_variant OV-AU 22 41542781 41542781 single base substitution G C missense_variant V698L 2092G>C OV-AU 22 41556640 41556640 single base substitution C T splice_region_variant OV-AU 22 41557760 41557760 single base substitution G A intron_variant OV-AU 22 41560745 41560745 single base substitution C T intron_variant OV-AU 22 41570460 41570460 single base substitution G C intron_variant OV-AU 22 41578710 41578710 single base substitution G A downstream_gene_variant PACA-AU 22 41482945 41482945 single base substitution C A upstream_gene_variant PACA-AU 22 41483017 41483017 single base substitution T C upstream_gene_variant PACA-AU 22 41489951 41489951 single base substitution C T intron_variant PACA-AU 22 41492580 41492582 deletion of <=200bp GGA - intron_variant PACA-AU 22 41498377 41498377 single base substitution G A intron_variant PACA-AU 22 41498625 41498625 single base substitution G A intron_variant PACA-AU 22 41508717 41508717 single base substitution T G intron_variant PACA-AU 22 41510183 41510183 single base substitution T C intron_variant PACA-AU 22 41513307 41513307 single base substitution G C missense_variant V71L 211G>C PACA-AU 22 41514316 41514316 single base substitution C A intron_variant PACA-AU 22 41515189 41515189 single base substitution T A intron_variant PACA-AU 22 41517314 41517314 single base substitution T G intron_variant PACA-AU 22 41517315 41517315 single base substitution G T intron_variant PACA-AU 22 41518217 41518217 single base substitution A T intron_variant PACA-AU 22 41520289 41520289 single base substitution T A intron_variant PACA-AU 22 41522824 41522824 single base substitution C G intron_variant PACA-AU 22 41524443 41524443 single base substitution C T intron_variant PACA-AU 22 41533606 41533606 single base substitution G A intron_variant PACA-AU 22 41534613 41534613 deletion of <=200bp T - intron_variant PACA-AU 22 41545734 41545734 single base substitution T C intron_variant PACA-AU 22 41551484 41551484 single base substitution C T intron_variant PACA-AU 22 41554489 41554500 deletion of <=200bp ACAGTTACCAGA - inframe_deletion YSYQN1192Y PACA-AU 22 41560088 41560112 deletion of <=200bp ATGCATCAGATCTGTGTCCTTCACC - frameshift_variant MHQICVLHH1254 PACA-AU 22 41560415 41560415 single base substitution A C intron_variant PACA-AU 22 41568233 41568237 deletion of <=200bp AGGAT - intron_variant PACA-AU 22 41568507 41568507 insertion of <=200bp - T frameshift_variant I1486I? PACA-AU 22 41570006 41570006 single base substitution C T intron_variant PACA-AU 22 41573283 41573283 single base substitution G A synonymous_variant T1856T 5568G>A PACA-AU 22 41575884 41575884 single base substitution T A 3_prime_UTR_variant PACA-AU 22 41578185 41578185 single base substitution C G downstream_gene_variant PACA-CA 22 41484909 41484917 deletion of <=200bp CACATTTCT - upstream_gene_variant PACA-CA 22 41485955 41485955 single base substitution G A upstream_gene_variant PACA-CA 22 41486038 41486038 single base substitution C G upstream_gene_variant PACA-CA 22 41486062 41486062 single base substitution A T upstream_gene_variant PACA-CA 22 41486212 41486212 single base substitution G T upstream_gene_variant PACA-CA 22 41487709 41487709 single base substitution C A upstream_gene_variant PACA-CA 22 41487769 41487769 single base substitution G A upstream_gene_variant PACA-CA 22 41489154 41489154 single base substitution G C intron_variant PACA-CA 22 41490992 41490992 single base substitution A T intron_variant PACA-CA 22 41493799 41493799 single base substitution T C intron_variant PACA-CA 22 41493953 41493953 single base substitution C T intron_variant PACA-CA 22 41496180 41496180 single base substitution A G intron_variant PACA-CA 22 41497208 41497208 single base substitution A T intron_variant PACA-CA 22 41498020 41498020 deletion of <=200bp T - intron_variant PACA-CA 22 41500248 41500248 single base substitution C T intron_variant PACA-CA 22 41501020 41501020 single base substitution T A intron_variant PACA-CA 22 41503203 41503203 insertion of <=200bp - A intron_variant PACA-CA 22 41505390 41505390 single base substitution A G intron_variant PACA-CA 22 41506131 41506131 single base substitution C T intron_variant PACA-CA 22 41507396 41507396 single base substitution T C intron_variant PACA-CA 22 41509547 41509547 single base substitution T C intron_variant PACA-CA 22 41509845 41509845 single base substitution C T intron_variant PACA-CA 22 41511335 41511335 single base substitution A G intron_variant PACA-CA 22 41518431 41518431 single base substitution A G intron_variant PACA-CA 22 41518432 41518432 single base substitution A T intron_variant PACA-CA 22 41518433 41518433 single base substitution G T intron_variant PACA-CA 22 41521225 41521225 single base substitution C G intron_variant PACA-CA 22 41522232 41522232 single base substitution T G intron_variant PACA-CA 22 41525325 41525325 single base substitution A G intron_variant PACA-CA 22 41526640 41526640 single base substitution G A intron_variant PACA-CA 22 41528717 41528719 deletion of <=200bp ATG - intron_variant PACA-CA 22 41531686 41531686 single base substitution A G intron_variant PACA-CA 22 41534922 41534922 single base substitution C T intron_variant PACA-CA 22 41535466 41535466 single base substitution T A intron_variant PACA-CA 22 41535667 41535667 single base substitution G A intron_variant PACA-CA 22 41540243 41540243 single base substitution T C intron_variant PACA-CA 22 41541314 41541314 single base substitution G C intron_variant PACA-CA 22 41541349 41541349 single base substitution A G intron_variant PACA-CA 22 41542838 41542838 single base substitution T A intron_variant PACA-CA 22 41546520 41546520 single base substitution G A intron_variant PACA-CA 22 41552323 41552323 single base substitution G A intron_variant PACA-CA 22 41555725 41555725 single base substitution C G intron_variant PACA-CA 22 41557163 41557163 single base substitution C T intron_variant PACA-CA 22 41559693 41559693 single base substitution G T intron_variant PACA-CA 22 41559845 41559845 single base substitution G A intron_variant PACA-CA 22 41564080 41564080 single base substitution C T intron_variant PACA-CA 22 41568210 41568210 single base substitution A G intron_variant PACA-CA 22 41570235 41570235 single base substitution G A intron_variant PACA-CA 22 41571568 41571568 single base substitution C A intron_variant PACA-CA 22 41574128 41574128 single base substitution C T missense_variant A2138V 6413C>T PACA-CA 22 41578105 41578105 single base substitution T G downstream_gene_variant PACA-CA 22 41578941 41578969 deletion of <=200bp GCAGTGCCCCAGGTGCTGTCATTCACTTC - downstream_gene_variant PACA-CA 22 41579569 41579569 single base substitution A G downstream_gene_variant PAEN-AU 22 41501592 41501592 deletion of <=200bp G - intron_variant PAEN-IT 22 41495821 41495821 single base substitution A T intron_variant PAEN-IT 22 41504254 41504254 single base substitution T C intron_variant PAEN-IT 22 41517306 41517306 single base substitution A T intron_variant PAEN-IT 22 41573101 41573101 single base substitution T G missense_variant C1796G 5386T>G PBCA-DE 22 41484468 41484468 single base substitution C T upstream_gene_variant PBCA-DE 22 41486166 41486166 insertion of <=200bp - A upstream_gene_variant PBCA-DE 22 41487704 41487704 single base substitution A C upstream_gene_variant PBCA-DE 22 41489154 41489154 single base substitution G A intron_variant PBCA-DE 22 41510829 41510829 insertion of <=200bp - A intron_variant PBCA-DE 22 41524920 41524920 single base substitution C T intron_variant PBCA-DE 22 41525891 41525891 single base substitution T C splice_region_variant PBCA-DE 22 41529329 41529329 insertion of <=200bp - T intron_variant PBCA-DE 22 41556451 41556451 single base substitution A C intron_variant PBCA-DE 22 41558061 41558061 single base substitution G A intron_variant PBCA-DE 22 41574348 41574348 single base substitution C A missense_variant F2211L 6633C>A PRAD-CA 22 41484842 41484842 single base substitution C A upstream_gene_variant PRAD-CA 22 41497336 41497336 single base substitution A G intron_variant PRAD-CA 22 41533932 41533932 single base substitution T C intron_variant PRAD-CA 22 41537683 41537683 single base substitution C T intron_variant PRAD-CA 22 41552730 41552730 single base substitution C A intron_variant PRAD-CA 22 41563616 41563616 single base substitution A G intron_variant PRAD-CA 22 41566982 41566982 single base substitution T A intron_variant PRAD-CA 22 41572575 41572575 single base substitution G A intron_variant PRAD-CA 22 41580504 41580504 single base substitution C G downstream_gene_variant PRAD-UK 22 41482894 41482894 single base substitution G C upstream_gene_variant PRAD-UK 22 41488902 41488902 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant PRAD-UK 22 41500951 41500951 single base substitution G A intron_variant PRAD-UK 22 41525266 41525266 single base substitution C T intron_variant PRAD-UK 22 41525679 41525679 single base substitution T C intron_variant PRAD-UK 22 41530133 41530133 single base substitution T G intron_variant PRAD-UK 22 41541161 41541161 single base substitution T C intron_variant PRAD-UK 22 41548756 41548756 single base substitution C T intron_variant PRAD-UK 22 41549524 41549524 single base substitution C T intron_variant PRAD-UK 22 41560725 41560725 single base substitution A T intron_variant PRAD-UK 22 41562886 41562886 single base substitution C A intron_variant PRAD-UK 22 41569094 41569094 single base substitution C T intron_variant PRAD-US 22 41573200 41573200 single base substitution C T missense_variant R1829C 5485C>T PRAD-US 22 41573205 41573205 single base substitution G T missense_variant R1830S 5490G>T PRAD-US 22 41573944 41573944 single base substitution A G missense_variant N2077D 6229A>G PRAD-US 22 41573977 41573977 single base substitution C T missense_variant R2088W 6262C>T READ-US 22 41513193 41513193 single base substitution T G missense_variant F33V 97T>G READ-US 22 41513646 41513646 single base substitution C T stop_gained Q184* 550C>T READ-US 22 41523526 41523526 single base substitution C T synonymous_variant G314G 942C>T READ-US 22 41533773 41533773 single base substitution G A missense_variant R580Q 1739G>A READ-US 22 41572335 41572335 single base substitution G A missense_variant D1622N 4864G>A READ-US 22 41574679 41574679 deletion of <=200bp C - frameshift_variant P2322 RECA-EU 22 41485148 41485148 single base substitution G T upstream_gene_variant RECA-EU 22 41488715 41488715 single base substitution A G 5_prime_UTR_variant RECA-EU 22 41494004 41494004 single base substitution T A intron_variant RECA-EU 22 41494782 41494782 single base substitution C T intron_variant RECA-EU 22 41495823 41495823 single base substitution G A intron_variant RECA-EU 22 41500739 41500739 single base substitution T G intron_variant RECA-EU 22 41516601 41516601 single base substitution T A intron_variant RECA-EU 22 41517481 41517481 single base substitution G A intron_variant RECA-EU 22 41518161 41518161 single base substitution C T intron_variant RECA-EU 22 41520214 41520214 single base substitution G C intron_variant RECA-EU 22 41534954 41534954 single base substitution G T intron_variant RECA-EU 22 41535645 41535645 single base substitution C A intron_variant RECA-EU 22 41538153 41538153 single base substitution G A intron_variant RECA-EU 22 41555161 41555161 single base substitution C T intron_variant RECA-EU 22 41565035 41565035 single base substitution C T intron_variant SKCA-BR 22 41484011 41484011 insertion of <=200bp - AAAAAAAGAAAAGAAAAG upstream_gene_variant SKCA-BR 22 41484011 41484011 insertion of <=200bp - AAAAAAAG upstream_gene_variant SKCA-BR 22 41487494 41487494 single base substitution T C upstream_gene_variant SKCA-BR 22 41487564 41487564 single base substitution G A upstream_gene_variant SKCA-BR 22 41487635 41487635 single base substitution C T upstream_gene_variant SKCA-BR 22 41487669 41487669 single base substitution G C upstream_gene_variant SKCA-BR 22 41491552 41491552 insertion of <=200bp - AT intron_variant SKCA-BR 22 41492162 41492162 single base substitution C T intron_variant SKCA-BR 22 41493931 41493931 single base substitution C T intron_variant SKCA-BR 22 41499411 41499411 single base substitution T G intron_variant SKCA-BR 22 41500389 41500389 single base substitution G T intron_variant SKCA-BR 22 41500486 41500486 single base substitution G T intron_variant SKCA-BR 22 41504248 41504248 single base substitution C T intron_variant SKCA-BR 22 41505273 41505273 single base substitution C A intron_variant SKCA-BR 22 41506420 41506420 single base substitution C T intron_variant SKCA-BR 22 41509161 41509161 single base substitution A C intron_variant SKCA-BR 22 41511530 41511530 single base substitution G A intron_variant SKCA-BR 22 41515170 41515170 insertion of <=200bp - CTTATTA intron_variant SKCA-BR 22 41515179 41515179 single base substitution A T intron_variant SKCA-BR 22 41515180 41515180 insertion of <=200bp - TTATTA intron_variant SKCA-BR 22 41515183 41515183 single base substitution T A intron_variant SKCA-BR 22 41515186 41515186 single base substitution T A intron_variant SKCA-BR 22 41515492 41515492 single base substitution G T intron_variant SKCA-BR 22 41518144 41518148 deletion of <=200bp TTTTC - intron_variant SKCA-BR 22 41521349 41521349 single base substitution C T intron_variant SKCA-BR 22 41521848 41521858 deletion of <=200bp CTTTTGTTTCT - intron_variant SKCA-BR 22 41525172 41525172 insertion of <=200bp - GC intron_variant SKCA-BR 22 41525180 41525180 insertion of <=200bp - AT intron_variant SKCA-BR 22 41528289 41528290 deletion of <=200bp TC - intron_variant SKCA-BR 22 41528323 41528323 single base substitution C A intron_variant SKCA-BR 22 41531825 41531825 single base substitution C T missense_variant P513S 1537C>T SKCA-BR 22 41535884 41535884 single base substitution C T intron_variant SKCA-BR 22 41540831 41540831 single base substitution C T intron_variant SKCA-BR 22 41543566 41543566 single base substitution C T intron_variant SKCA-BR 22 41547405 41547405 single base substitution A C intron_variant SKCA-BR 22 41552615 41552615 single base substitution C T intron_variant SKCA-BR 22 41561189 41561189 single base substitution C T intron_variant SKCA-BR 22 41562124 41562124 single base substitution A T intron_variant SKCA-BR 22 41563453 41563453 single base substitution C T intron_variant SKCA-BR 22 41563818 41563818 insertion of <=200bp - GGTT intron_variant SKCA-BR 22 41563818 41563818 insertion of <=200bp - GGTTTT intron_variant SKCA-BR 22 41563819 41563819 single base substitution T G intron_variant SKCA-BR 22 41569851 41569851 single base substitution C T intron_variant SKCA-BR 22 41570827 41570827 single base substitution C T intron_variant SKCA-BR 22 41572460 41572460 single base substitution G T missense_variant Q1663H 4989G>T SKCA-BR 22 41572739 41572739 single base substitution C T intron_variant SKCA-BR 22 41573268 41573268 single base substitution T C synonymous_variant T1851T 5553T>C SKCA-BR 22 41578462 41578462 single base substitution G A downstream_gene_variant SKCM-US 22 41513752 41513752 single base substitution T C missense_variant L219P 656T>C SKCM-US 22 41523662 41523662 single base substitution G A missense_variant E360K 1078G>A SKCM-US 22 41527608 41527608 single base substitution C T missense_variant P500L 1499C>T SKCM-US 22 41533698 41533698 single base substitution C T missense_variant P555L 1664C>T SKCM-US 22 41537070 41537070 single base substitution C T synonymous_variant L633L 1897C>T SKCM-US 22 41545778 41545778 single base substitution G A missense_variant S798N 2393G>A SKCM-US 22 41545984 41545984 single base substitution C T missense_variant P867S 2599C>T SKCM-US 22 41551054 41551054 single base substitution C T synonymous_variant Y1066Y 3198C>T SKCM-US 22 41553271 41553271 single base substitution T C synonymous_variant D1120D 3360T>C SKCM-US 22 41556650 41556650 single base substitution C T missense_variant H1199Y 3595C>T SKCM-US 22 41556696 41556696 single base substitution C T missense_variant S1214F 3641C>T SKCM-US 22 41564759 41564759 single base substitution C T missense_variant P1354S 4060C>T SKCM-US 22 41564798 41564798 single base substitution G T missense_variant D1367Y 4099G>T SKCM-US 22 41572350 41572350 single base substitution C T missense_variant R1627W 4879C>T SKCM-US 22 41572389 41572389 single base substitution G T stop_gained E1640* 4918G>T SKCM-US 22 41572463 41572463 single base substitution C T synonymous_variant D1664D 4992C>T SKCM-US 22 41573197 41573197 single base substitution C T missense_variant L1828F 5482C>T SKCM-US 22 41573345 41573345 single base substitution C T missense_variant P1877L 5630C>T SKCM-US 22 41573426 41573426 single base substitution A C missense_variant Q1904P 5711A>C SKCM-US 22 41573662 41573662 single base substitution G A missense_variant G1983R 5947G>A SKCM-US 22 41573875 41573875 single base substitution C T missense_variant L2054F 6160C>T STAD-US 22 41489028 41489028 single base substitution A G missense_variant E7G 20A>G STAD-US 22 41513540 41513540 single base substitution G A synonymous_variant T148T 444G>A STAD-US 22 41513716 41513716 single base substitution A G missense_variant Y207C 620A>G STAD-US 22 41523566 41523566 single base substitution C T missense_variant H328Y 982C>T STAD-US 22 41523693 41523693 single base substitution G A missense_variant R370H 1109G>A STAD-US 22 41527551 41527551 single base substitution C T missense_variant P481L 1442C>T STAD-US 22 41527639 41527639 single base substitution T C splice_donor_variant STAD-US 22 41533773 41533773 single base substitution G A missense_variant R580Q 1739G>A STAD-US 22 41543950 41543950 single base substitution G A splice_region_variant STAD-US 22 41545050 41545050 single base substitution C T synonymous_variant G750G 2250C>T STAD-US 22 41545781 41545781 insertion of <=200bp - T frameshift_variant S799F? STAD-US 22 41545782 41545782 insertion of <=200bp - T frameshift_variant S799S? STAD-US 22 41556645 41556645 single base substitution G T splice_acceptor_variant STAD-US 22 41564766 41564766 single base substitution G A missense_variant R1356Q 4067G>A STAD-US 22 41566511 41566511 single base substitution T G missense_variant L1463R 4388T>G STAD-US 22 41566520 41566520 single base substitution G T missense_variant W1466L 4397G>T STAD-US 22 41572350 41572350 single base substitution C T missense_variant R1627W 4879C>T STAD-US 22 41572924 41572924 single base substitution C T missense_variant R1737C 5209C>T STAD-US 22 41573174 41573174 single base substitution A G missense_variant H1820R 5459A>G STAD-US 22 41573763 41573763 single base substitution G A missense_variant M2016I 6048G>A STAD-US 22 41574128 41574128 single base substitution C T missense_variant A2138V 6413C>T STAD-US 22 41574331 41574331 single base substitution G T missense_variant A2206S 6616G>T STAD-US 22 41574435 41574435 single base substitution A G synonymous_variant G2240G 6720A>G STAD-US 22 41574595 41574595 single base substitution C A missense_variant L2294I 6880C>A STAD-US 22 41574817 41574817 single base substitution G A missense_variant D2368N 7102G>A THCA-SA 22 41548008 41548008 single base substitution A G missense_variant I997V 2989A>G THCA-SA 22 41551039 41551039 single base substitution T A synonymous_variant T1061T 3183T>A UCEC-US 22 41513189 41513189 single base substitution A G splice_acceptor_variant UCEC-US 22 41513277 41513277 deletion of <=200bp A - frameshift_variant I61 UCEC-US 22 41521884 41521884 single base substitution A G missense_variant N249S 746A>G UCEC-US 22 41523520 41523520 single base substitution G T missense_variant Q312H 936G>T UCEC-US 22 41527545 41527545 single base substitution A C missense_variant Q479P 1436A>C UCEC-US 22 41531815 41531815 single base substitution A G splice_acceptor_variant UCEC-US 22 41531831 41531831 single base substitution G T stop_gained G515* 1543G>T UCEC-US 22 41533773 41533773 single base substitution G A missense_variant R580Q 1739G>A UCEC-US 22 41536179 41536179 single base substitution C A missense_variant A599D 1796C>A UCEC-US 22 41542813 41542813 single base substitution A G synonymous_variant P708P 2124A>G UCEC-US 22 41546174 41546174 single base substitution C T missense_variant P930L 2789C>T UCEC-US 22 41547839 41547839 single base substitution T G splice_region_variant UCEC-US 22 41548329 41548329 single base substitution G A synonymous_variant P1039P 3117G>A UCEC-US 22 41553213 41553213 single base substitution C T missense_variant T1101I 3302C>T UCEC-US 22 41553249 41553249 single base substitution A T missense_variant E1113V 3338A>T UCEC-US 22 41553266 41553266 single base substitution G A missense_variant D1119N 3355G>A UCEC-US 22 41553288 41553288 single base substitution A G missense_variant N1126S 3377A>G UCEC-US 22 41554474 41554474 single base substitution G A missense_variant R1187H 3560G>A UCEC-US 22 41558739 41558739 single base substitution A C missense_variant K1228N 3684A>C UCEC-US 22 41562606 41562606 single base substitution C T synonymous_variant F1270F 3810C>T UCEC-US 22 41562637 41562637 single base substitution C T stop_gained R1281* 3841C>T UCEC-US 22 41562638 41562638 single base substitution G A missense_variant R1281Q 3842G>A UCEC-US 22 41562649 41562649 single base substitution G T stop_gained E1285* 3853G>T UCEC-US 22 41564555 41564555 single base substitution T C missense_variant V1326A 3977T>C UCEC-US 22 41564750 41564750 single base substitution G T stop_gained E1351* 4051G>T UCEC-US 22 41565523 41565523 single base substitution T G missense_variant Y1397D 4189T>G UCEC-US 22 41566475 41566475 single base substitution A G missense_variant H1451R 4352A>G UCEC-US 22 41568517 41568517 insertion of <=200bp - G frameshift_variant Q1489Q? UCEC-US 22 41568562 41568562 single base substitution C T synonymous_variant F1504F 4512C>T UCEC-US 22 41572357 41572357 single base substitution C T missense_variant A1629V 4886C>T UCEC-US 22 41572404 41572404 single base substitution C T stop_gained R1645* 4933C>T UCEC-US 22 41572485 41572485 single base substitution G T stop_gained E1672* 5014G>T UCEC-US 22 41573557 41573557 single base substitution T A missense_variant F1948I 5842T>A UCEC-US 22 41573965 41573965 single base substitution T G missense_variant F2084V 6250T>G UCEC-US 22 41574607 41574607 single base substitution C T stop_gained Q2298* 6892C>T UCEC-US 22 41574665 41574665 single base substitution G T missense_variant R2317L 6950G>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand ESCC-F34 COSM5047562 c.3778_3780delCTT p.L1260delL Deletion - In frame 22:41164102-41164104 + UD-SCC-2 COSM4300068 c.1681C>T p.Q561* Substitution - Nonsense 22:41137711-41137711 + ATL276 COSM5707677 c.4079T>C p.L1360P Substitution - Missense 22:41168774-41168774 + CHC1055T COSM217240 c.1169T>G p.V390G Substitution - Missense 22:41129890-41129890 + P100 COSM3153108 c.1927G>T p.E643* Substitution - Nonsense 22:41141096-41141096 + 1N04-VS-1T04 COSM4972749 c.1684C>T p.P562S Substitution - Missense 22:41137714-41137714 + SH-6055 COSM5020527 c.1168+7G>C p.? Unknown 22:41127755-41127755 + 2432704 COSM5352295 c.? p.R2185Q Substitution - Missense HN_63021 COSM127889 c.1881G>A p.A627A Substitution - coding silent 22:41141050-41141050 + TCGA-AX-A0J0-01 COSM1034546 c.3684A>C p.K1228N Substitution - Missense 22:41162735-41162735 + ATL161 COSM5707679 c.4843delC p.P1615fs*9 Deletion - Frameshift 22:41176310-41176310 + HT29 COSM96442 c.4401_4402insA p.M1470fs*3 Insertion - Frameshift 22:41170520-41170521 + TCGA-24-1471-01 COSM78937 c.3934C>T p.R1312* Substitution - Nonsense 22:41168508-41168508 + PD6784a COSM4385256 c.4102G>A p.G1368S Substitution - Missense 22:41168797-41168797 + TCGA-EE-A3JB-06 COSM4898642 c.4918G>T p.E1640* Substitution - Nonsense 22:41176385-41176385 + TCGA-AG-A002-01 COSM260693 c.7121C>A p.S2374Y Substitution - Missense 22:41178832-41178832 + 587224 COSM1205370 c.1651C>T p.P551S Substitution - Missense 22:41137681-41137681 + sysucc-1397T COSM4984100 c.512C>T p.A171V Substitution - Missense 22:41117604-41117604 + S07-16280-TP COSM4991526 c.1015C>T p.Q339* Substitution - Nonsense 22:41127595-41127595 + 2228010 COSM4171998 c.? p.C369F Substitution - Missense I2L-P23-Tumor-Organoid COSM96442 c.4401_4402insA p.M1470fs*3 Insertion - Frameshift 22:41170520-41170521 + PD6781a COSM4385255 c.3788A>T p.E1263V Substitution - Missense 22:41164112-41164112 + sysucc-1030T COSM5452327 c.3098C>T p.S1033L Substitution - Missense 22:41152306-41152306 + ATL171 COSM88784 c.4879C>T p.R1627W Substitution - Missense 22:41176346-41176346 + 1N27-VS-1T27 COSM4973677 c.6004C>T p.Q2002* Substitution - Nonsense 22:41177715-41177715 + S01524 COSM318353 c.3358G>T p.D1120Y Substitution - Missense 22:41157265-41157265 + V29 COSM4387473 c.4505C>T p.P1502L Substitution - Missense 22:41172551-41172551 + CSCC-35-T COSM4479718 c.2350C>T p.P784S Substitution - Missense 22:41149146-41149146 + S02194 COSM5674886 c.5305A>G p.K1769E Substitution - Missense 22:41177016-41177016 + HCC105 COSM1034534 c.3117G>A p.P1039P Substitution - coding silent 22:41152325-41152325 + PA285 COSM1163312 c.2546T>C p.I849T Substitution - Missense 22:41149927-41149927 + LIM-2405 COSM96442 c.4401_4402insA p.M1470fs*3 Insertion - Frameshift 22:41170520-41170521 + TCGA-A3-3320-01 COSM1495212 c.6226G>T p.A2076S Substitution - Missense 22:41177937-41177937 + ESCC_162 COSM5647885 c.202C>G p.L68V Substitution - Missense 22:41117294-41117294 + TCGA-02-2483-01 COSM3748173 c.4041A>G p.G1347G Substitution - coding silent 22:41168736-41168736 + TCGA-BH-A0DZ-01 COSM445043 c.6023C>T p.S2008F Substitution - Missense 22:41177734-41177734 + S00830 COSM317283 c.3857A>G p.N1286S Substitution - Missense 22:41166649-41166649 + H1703 COSM1196512 c.4310C>T p.A1437V Substitution - Missense 22:41170429-41170429 + 2011-2327:2012-308-T COSM4605343 c.4230G>T p.R1410S Substitution - Missense 22:41169560-41169560 + FL19 COSM96543 c.? p.Q2210_Q2213del Deletion - In frame ESCC_BICR_071T COSM13867 c.4355C>T p.P1452L Substitution - Missense 22:41170474-41170474 + PD10793a COSM5225999 c.3502-1G>T p.? Unknown 22:41158411-41158411 + B89-4 COSM254672 c.4352A>T p.H1451L Substitution - Missense 22:41170471-41170471 + AOCS-146-1-9 COSM4137485 c.3591-6C>T p.? Unknown 22:41160636-41160636 + UM-SCC-2 COSM4599296 c.1192C>T p.Q398* Substitution - Nonsense 22:41129913-41129913 + TCGA-HU-A4GN-01 COSM4104430 c.1442C>T p.P481L Substitution - Missense 22:41131547-41131547 + 103 COSM4169968 c.95-1G>A p.? Unknown 22:41117186-41117186 + 1523835 COSM96433 c.5095delA p.N1700fs*9 Deletion - Frameshift 22:41176806-41176806 + ATL320 COSM96440 c.256C>T p.R86* Substitution - Nonsense 22:41117348-41117348 + tumor_4138885 COSM5789312 c.4228A>T p.R1410W Substitution - Missense 22:41169558-41169558 + TCGA-18-3409-01 COSM727027 c.4893C>T p.L1631L Substitution - coding silent 22:41176360-41176360 + CSCC-27-T COSM4516858 c.2403_2404CC>TT p.P802S Substitution - Missense 22:41149784-41149785 + N-Thy002 COSM5094809 c.2680_2681insT p.P894fs*15 Insertion - Frameshift 22:41150061-41150062 + 447 COSM4435124 c.4505C>G p.P1502R Substitution - Missense 22:41172551-41172551 + TCGA-D3-A3MU-06 COSM3554891 c.4992C>T p.D1664D Substitution - coding silent 22:41176459-41176459 + TCGA-D1-A103-01 COSM1034534 c.3117G>A p.P1039P Substitution - coding silent 22:41152325-41152325 + T3118 COSM4681089 c.1785G>A p.P595P Substitution - coding silent 22:41140164-41140164 + TCGA-D1-A160-01 COSM1034519 c.1529-2A>G p.? Unknown 22:41135811-41135811 + KYSE110 COSM5049516 c.4199G>A p.S1400N Substitution - Missense 22:41169529-41169529 + S00830 COSM317283 c.3857A>G p.N1286S Substitution - Missense 22:41166649-41166649 + TCGA-F5-6814-01 COSM3424202 c.97T>G p.F33V Substitution - Missense 22:41117189-41117189 + TCGA-CG-5721-01 COSM4104442 c.6720A>G p.G2240G Substitution - coding silent 22:41178431-41178431 + sysucc-1116T COSM5483073 c.1612A>C p.N538H Substitution - Missense 22:41135896-41135896 + ESCC_153 COSM122851 c.4195G>A p.D1399N Substitution - Missense 22:41169525-41169525 + TCGA-J4-A67M-01 COSM3783562 c.5490G>T p.R1830S Substitution - Missense 22:41177201-41177201 + QC2-17-T2 COSM3357344 c.4399T>G p.Y1467D Substitution - Missense 22:41170518-41170518 + B90 COSM254673 c.4561G>C p.E1521Q Substitution - Missense 22:41172607-41172607 + TCGA-EA-A3QD-01 COSM4821763 c.3935G>A p.R1312Q Substitution - Missense 22:41168509-41168509 + V208 COSM4387469 c.4307G>T p.W1436L Substitution - Missense 22:41170426-41170426 + YUKLAB COSM1714418 c.1099_1100CC>TT p.P367F Substitution - Missense 22:41127679-41127680 + SW620 COSM1682288 c.4319C>T p.P1440L Substitution - Missense 22:41170438-41170438 + 2218663 COSM4169705 c.? p.P925T Substitution - Missense ESCC-F25 COSM5047408 c.758A>G p.Y253C Substitution - Missense 22:41125892-41125892 + TCGA-D5-6931-01 COSM1416468 c.1759C>T p.L587F Substitution - Missense 22:41137789-41137789 + 6 COSM5762874 c.1352C>A p.P451H Substitution - Missense 22:41131457-41131457 + V47 COSM727028 c.4241A>G p.Y1414C Substitution - Missense 22:41169571-41169571 + SJLGG009_D COSM1682287 c.4066C>T p.R1356* Substitution - Nonsense 22:41168761-41168761 + ccRCC-35 COSM1661671 c.7109A>T p.N2370I Substitution - Missense 22:41178820-41178820 + 587286 COSM1205366 c.1190G>A p.R397Q Substitution - Missense 22:41129911-41129911 + CSCC-4-T COSM4476638 c.2083C>T p.R695C Substitution - Missense 22:41146768-41146768 + DM4 COSM5608364 c.4714G>T p.G1572W Substitution - Missense 22:41173719-41173719 + 2135 COSM88787 c.6574_6585del12 p.Q2192_Q2195delQQQQ Deletion - In frame 22:41178285-41178296 + DM4 COSM5608363 c.2293C>T p.L765F Substitution - Missense 22:41149089-41149089 + OSCC-GB_00530111 COSM4883298 c.1659G>A p.L553L Substitution - coding silent 22:41137689-41137689 + TCGA-FD-A3B8-01 COSM1308205 c.2485C>T p.Q829* Substitution - Nonsense 22:41149866-41149866 + PD6100a COSM4385252 c.3566C>T p.A1189V Substitution - Missense 22:41158476-41158476 + TCGA-06-0214-01 COSM3405689 c.4111C>T p.L1371L Substitution - coding silent 22:41168806-41168806 + LB771-HNC COSM13867 c.4355C>T p.P1452L Substitution - Missense 22:41170474-41170474 + B66 COSM255052 c.4372_4377delCCCAAG p.P1460_K1461delPK Deletion - In frame 22:41170491-41170496 + TCGA-EB-A5SE-01 COSM3554883 c.1664C>T p.P555L Substitution - Missense 22:41137694-41137694 + J85_T COSM3964351 c.3806+8T>G p.? Unknown 22:41164138-41164138 + 13D COSM1235064 c.4874A>T p.D1625V Substitution - Missense 22:41176341-41176341 + TCGA-HU-A4GT-01 COSM4104443 c.6880C>A p.L2294I Substitution - Missense 22:41178591-41178591 + ACINAR29 COSM1734466 c.743A>C p.N248T Substitution - Missense 22:41125877-41125877 + CHC303T COSM4957844 c.6223C>A p.H2075N Substitution - Missense 22:41177934-41177934 + S07-16280-TP COSM88788 c.187C>T p.Q63* Substitution - Nonsense 22:41117279-41117279 + D10 COSM5007088 c.5698A>T p.K1900* Substitution - Nonsense 22:41177409-41177409 + PD13775a COSM5024939 c.6114C>G p.I2038M Substitution - Missense 22:41177825-41177825 + TCGA-GV-A3JZ-01 COSM1308202 c.1891C>G p.H631D Substitution - Missense 22:41141060-41141060 + ATL344 COSM5707673 c.1760+1_1760+4delGTAA p.? Unknown 22:41137791-41137794 + SW48 COSM3153169 c.4402delA p.M1470fs*26 Deletion - Frameshift 22:41170521-41170521 + TCGA-AX-A05Z-01 COSM1034538 c.3338A>T p.E1113V Substitution - Missense 22:41157245-41157245 + TCGA-BR-4361-01 COSM4104428 c.982C>T p.H328Y Substitution - Missense 22:41127562-41127562 + TCGA-66-2773-01 COSM727025 c.6367G>T p.G2123W Substitution - Missense 22:41178078-41178078 + LB647-SCLC COSM27189 c.5850G>T p.R1950S Substitution - Missense 22:41177561-41177561 + CSCC-60-T COSM4466772 c.1451C>T p.P484L Substitution - Missense 22:41131556-41131556 + TCGA-D1-A16F-01 COSM1034528 c.2124A>G p.P708P Substitution - coding silent 22:41146809-41146809 + CoCa18 COSM96425 c.6662C>A p.P2221Q Substitution - Missense 22:41178373-41178373 + Pat_63_B COSM5859452 c.502G>A p.G168R Substitution - Missense 22:41117594-41117594 + TCGA-EI-6507-01 COSM1566439 c.6964delC p.H2324fs*29 Deletion - Frameshift 22:41178675-41178675 + SH-5693 COSM5020281 c.2019T>C p.P673P Substitution - coding silent 22:41141188-41141188 + 2432710 COSM5352296 c.? p.V279A Substitution - Missense S12-11594-TP COSM4991531 c.4136A>G p.Q1379R Substitution - Missense 22:41168831-41168831 + 587234 COSM1205375 c.6645A>C p.Q2215H Substitution - Missense 22:41178356-41178356 + PT49 COSM5936703 c.5404C>T p.P1802S Substitution - Missense 22:41177115-41177115 + V35 COSM4387470 c.4343T>C p.F1448S Substitution - Missense 22:41170462-41170462 + CSCC-15-T COSM4517821 c.4354_4355CC>TT p.P1452F Substitution - Missense 22:41170473-41170474 + GCT27 COSM5749630 c.5608C>T p.Q1870* Substitution - Nonsense 22:41177319-41177319 + ESO-717 COSM96421 c.1738C>T p.R580* Substitution - Nonsense 22:41137768-41137768 + TCGA-22-4595-01 COSM727024 c.6375C>A p.H2125Q Substitution - Missense 22:41178086-41178086 + SC-her2-049 COSM4943270 c.7192G>A p.D2398N Substitution - Missense 22:41178903-41178903 + TCGA-DC-6682-01 COSM1566443 c.550C>T p.Q184* Substitution - Nonsense 22:41117642-41117642 + DM96 COSM5608372 c.2011C>T p.P671S Substitution - Missense 22:41141180-41141180 + SJLGG009 COSM1682287 c.4066C>T p.R1356* Substitution - Nonsense 22:41168761-41168761 + KM12 COSM1682285 c.2282A>G p.Q761R Substitution - Missense 22:41149078-41149078 + Ramos COSM88788 c.187C>T p.Q63* Substitution - Nonsense 22:41117279-41117279 + SNUH_G45_S1 COSM4002191 c.3348G>A p.Q1116Q Substitution - coding silent 22:41157255-41157255 + MBRep_T3 COSM215865 c.6633C>A p.F2211L Substitution - Missense 22:41178344-41178344 + TCGA-CU-A3KJ-01 COSM1308213 c.6174C>G p.L2058L Substitution - coding silent 22:41177885-41177885 + ME011T COSM224615 c.4925C>T p.S1642F Substitution - Missense 22:41176392-41176392 + LIM-2412 COSM96440 c.256C>T p.R86* Substitution - Nonsense 22:41117348-41117348 + B89-10 COSM255053 c.4377_4388del12 p.P1460_L1463delPKRL Deletion - In frame 22:41170496-41170507 + CSCC-55-T COSM4496927 c.4860C>T p.P1620P Substitution - coding silent 22:41176327-41176327 + TCGA-CU-A3KJ-01 COSM1308212 c.6123C>G p.L2041L Substitution - coding silent 22:41177834-41177834 + RK308_C01 COSM3740446 c.6788G>A p.R2263Q Substitution - Missense 22:41178499-41178499 + 2011-2351:2012-330-T COSM727028 c.4241A>G p.Y1414C Substitution - Missense 22:41169571-41169571 + TCGA-GF-A4EO-06 COSM3554888 c.3595C>T p.H1199Y Substitution - Missense 22:41160646-41160646 + SJHGG003_A COSM4968836 c.6102C>T p.G2034G Substitution - coding silent 22:41177813-41177813 + sysucc-1163T COSM5458947 c.1854C>T p.D618D Substitution - coding silent 22:41140233-41140233 + SUDHL6 COSM88784 c.4879C>T p.R1627W Substitution - Missense 22:41176346-41176346 + TCGA-BK-A0C9-01 COSM1034579 c.6892C>T p.Q2298* Substitution - Nonsense 22:41178603-41178603 + YUWAPO COSM5393733 c.1322G>A p.S441N Substitution - Missense 22:41131427-41131427 + TARGET-20-PANINI-09A-03D COSM5487677 c.3491G>A p.C1164Y Substitution - Missense 22:41157398-41157398 + QC2-11-T2 COSM5652357 c.6792C>T p.L2264L Substitution - coding silent 22:41178503-41178503 + T578 COSM4681090 c.1844T>G p.V615G Substitution - Missense 22:41140223-41140223 + SUDHL8 COSM88782 c.4710A>T p.K1570N Substitution - Missense 22:41173715-41173715 + Gp2D COSM3153189 c.4981C>T p.Q1661* Substitution - Nonsense 22:41176448-41176448 + 2217108 COSM4169403 c.? p.R604Q Substitution - Missense TCGA-EE-A29L-06 COSM3554881 c.1078G>A p.E360K Substitution - Missense 22:41127658-41127658 + TCGA-BR-8680-01 COSM4104440 c.6413C>T p.A2138V Substitution - Missense 22:41178124-41178124 + Pat_63_B COSM5859454 c.2539C>T p.P847S Substitution - Missense 22:41149920-41149920 + CHC1055T COSM217240 c.1169T>G p.V390G Substitution - Missense 22:41129890-41129890 + CHC1704T COSM4804090 c.1401C>G p.A467A Substitution - coding silent 22:41131506-41131506 + DM102 COSM5608360 c.3963C>T p.V1321V Substitution - coding silent 22:41168537-41168537 + 2228001 COSM4171997 c.? p.R2263* Substitution - Nonsense ESCC-D10 COSM5045248 c.3549C>A p.C1183* Substitution - Nonsense 22:41158459-41158459 + HCC2998 COSM1682289 c.4751T>G p.L1584R Substitution - Missense 22:41173756-41173756 + B89-4 COSM254672 c.4352A>T p.H1451L Substitution - Missense 22:41170471-41170471 + TCGA-EE-A2GS-06 COSM3554887 c.3198C>T p.Y1066Y Substitution - coding silent 22:41155050-41155050 + P60 COSM4002191 c.3348G>A p.Q1116Q Substitution - coding silent 22:41157255-41157255 + 2011-2349:2012-299-T COSM4603934 c.4617+1_4617+2insT p.? Unknown 22:41172664-41172665 + TCGA-DY-A1DD-01 COSM1566442 c.942C>T p.G314G Substitution - coding silent 22:41127522-41127522 + TCGA-GV-A3JX-01 COSM1308208 c.4578G>C p.E1526D Substitution - Missense 22:41172624-41172624 + SH-3327 COSM5019909 c.6636G>A p.Q2212Q Substitution - coding silent 22:41178347-41178347 + TCGA-IR-A3LK-01 COSM4817436 c.56C>G p.S19* Substitution - Nonsense 22:41093060-41093060 + DLD-1 COSM96434 c.? p.E1014* Substitution - Nonsense TCGA-EB-A430-01 COSM3554889 c.3641C>T p.S1214F Substitution - Missense 22:41160692-41160692 + B10-Tumor COSM254666 c.2620C>T p.Q874* Substitution - Nonsense 22:41150001-41150001 + TCGA-B5-A11G-01 COSM1034564 c.4352A>G p.H1451R Substitution - Missense 22:41170471-41170471 + ESCC_45 COSM5630366 c.6434T>A p.L2145Q Substitution - Missense 22:41178145-41178145 + TCGA-FV-A3R3-01 COSM4921819 c.4681A>G p.S1561G Substitution - Missense 22:41173686-41173686 + H748 COSM318352 c.3875-2A>G p.? Unknown 22:41168447-41168447 + TCGA-B5-A11E-01 COSM1034526 c.1796C>A p.A599D Substitution - Missense 22:41140175-41140175 + LU-1991 COSM5614887 c.34T>G p.S12A Substitution - Missense 22:41093038-41093038 + I2L-P23-Tumor-Biopsy COSM96442 c.4401_4402insA p.M1470fs*3 Insertion - Frameshift 22:41170520-41170521 + ESCC_BICR_044T COSM5439929 c.1965G>C p.Q655H Substitution - Missense 22:41141134-41141134 + TCGA-CU-A3KJ-01 COSM1308211 c.6004C>G p.Q2002E Substitution - Missense 22:41177715-41177715 + TCGA-BR-6566-01 COSM4104434 c.3591-1G>T p.? Unknown 22:41160641-41160641 + 2041 COSM88785 c.5711A>C p.Q1904P Substitution - Missense 22:41177422-41177422 + ESCC-123T COSM88793 c.4617+1G>A p.? Unknown 22:41172664-41172664 + YUSWI COSM1714421 c.3233C>T p.P1078L Substitution - Missense 22:41155085-41155085 + TCGA-BR-6852-01 COSM4104433 c.2250C>T p.G750G Substitution - coding silent 22:41149046-41149046 + TCGA-D3-A5GN-06 COSM3554886 c.2599C>T p.P867S Substitution - Missense 22:41149980-41149980 + T56 COSM1177798 c.5195G>A p.R1732H Substitution - Missense 22:41176906-41176906 + LIM2405 COSM4613573 c.2776_2777insC p.T928fs*21 Insertion - Frameshift 22:41150157-41150158 + TCGA-G9-6366-01 COSM1471496 c.6262C>T p.R2088W Substitution - Missense 22:41177973-41177973 + Pat_26_A COSM5859453 c.1561_1562GG>AA p.G521K Substitution - Missense 22:41135845-41135846 + S0051 COSM5883686 c.1678G>A p.A560T Substitution - Missense 22:41137708-41137708 + B66 COSM255052 c.4372_4377delCCCAAG p.P1460_K1461delPK Deletion - In frame 22:41170491-41170496 + 14 COSM5732949 c.6244G>A p.A2082T Substitution - Missense 22:41177955-41177955 + PD11110a COSM5945457 c.3488G>A p.C1163Y Substitution - Missense 22:41157395-41157395 + Sample_1 COSM4767796 c.3183T>A p.T1061T Substitution - coding silent 22:41155035-41155035 + MDA-MB-435S COSM96423 c.3038A>G p.E1013G Substitution - Missense 22:41152246-41152246 + TCGA-A6-6141-01 COSM1416478 c.3831G>T p.K1277N Substitution - Missense 22:41166623-41166623 + 090 COSM145369 c.5368T>G p.C1790G Substitution - Missense 22:41177079-41177079 + V21 COSM4387475 c.4538T>C p.L1513P Substitution - Missense 22:41172584-41172584 + B10 COSM254666 c.2620C>T p.Q874* Substitution - Nonsense 22:41150001-41150001 + HCT-15 COSM96511 c.3040G>T p.E1014* Substitution - Nonsense 22:41152248-41152248 + 255 COSM3731970 c.6949C>T p.R2317W Substitution - Missense 22:41178660-41178660 + TCGA-B9-5156-01 COSM3992197 c.61C>G p.P21A Substitution - Missense 22:41093065-41093065 + 2011-2348:2012-331-T COSM4603912 c.2313_2314insT p.S772fs*27 Insertion - Frameshift 22:41149109-41149110 + LN18 COSM3153168 c.4336T>A p.Y1446N Substitution - Missense 22:41170455-41170455 + S00472 COSM317282 c.4453-3C>G p.? Unknown 22:41172496-41172496 + ATL163 COSM3153235 c.6963_6964insC p.H2324fs*55 Insertion - Frameshift 22:41178674-41178675 + 186T COSM727028 c.4241A>G p.Y1414C Substitution - Missense 22:41169571-41169571 + DM79 COSM5608370 c.5245C>A p.R1749R Substitution - coding silent 22:41176956-41176956 + S02255 COSM5680743 c.4319C>G p.P1440R Substitution - Missense 22:41170438-41170438 + SBC7 COSM96419 c.4195G>T p.D1399Y Substitution - Missense 22:41169525-41169525 + TCGA-EP-A2KA-01 COSM4917326 c.5322A>T p.K1774N Substitution - Missense 22:41177033-41177033 + PD6823a COSM4385261 c.4600A>G p.S1534G Substitution - Missense 22:41172646-41172646 + T407 COSM1205370 c.1651C>T p.P551S Substitution - Missense 22:41137681-41137681 + L10 COSM5368945 c.3406T>C p.S1136P Substitution - Missense 22:41157313-41157313 + ESCC-F120 COSM5047132 c.3702delA p.N1236fs*41 Deletion - Frameshift 22:41162753-41162753 + 7_tFL COSM88784 c.4879C>T p.R1627W Substitution - Missense 22:41176346-41176346 + TCGA-C5-A7UH-01 COSM4856715 c.4934G>A p.R1645Q Substitution - Missense 22:41176401-41176401 + 6975 COSM5751372 c.5403C>AC p.C1801fs*1 Complex - frameshift 22:41177114-41177114 + TCGA-C5-A1MH-01 COSM4821120 c.1202C>G p.S401* Substitution - Nonsense 22:41129923-41129923 + DM14 COSM5608361 c.3589A>T p.R1197W Substitution - Missense 22:41158499-41158499 + 12-P8001 COSM4582439 c.1139C>T p.T380I Substitution - Missense 22:41127719-41127719 + V12 COSM580210 c.4453G>T p.D1485Y Substitution - Missense 22:41172499-41172499 + TCGA-CJ-6030-01 COSM478998 c.5279A>G p.K1760R Substitution - Missense 22:41176990-41176990 + PD6236a COSM4385232 c.38C>T p.A13V Substitution - Missense 22:41093042-41093042 + PD13775a COSM5024940 c.6255C>G p.I2085M Substitution - Missense 22:41177966-41177966 + HT-29 COSM96442 c.4401_4402insA p.M1470fs*3 Insertion - Frameshift 22:41170520-41170521 + 74 COSM4777992 c.4739T>C p.L1580P Substitution - Missense 22:41173744-41173744 + PD6163a COSM4385241 c.1672A>G p.T558A Substitution - Missense 22:41137702-41137702 + 2_PRE-TREATMENT COSM1721877 c.2524C>T p.P842S Substitution - Missense 22:41149905-41149905 + NPC2F COSM4997190 c.2407G>C p.V803L Substitution - Missense 22:41149788-41149788 + B86 COSM88784 c.4879C>T p.R1627W Substitution - Missense 22:41176346-41176346 + TCGA-EA-A5O9-01 COSM122851 c.4195G>A p.D1399N Substitution - Missense 22:41169525-41169525 + TCGA-AP-A0LQ-01 COSM1034550 c.3841C>T p.R1281* Substitution - Nonsense 22:41166633-41166633 + ESCC_162 COSM5647886 c.670C>T p.Q224* Substitution - Nonsense 22:41117762-41117762 + S05-45028-TP COSM4991535 c.4602C>T p.S1534S Substitution - coding silent 22:41172648-41172648 + TL42 COSM5751868 c.3695C>AC p.S1232fs*6 Complex - frameshift 22:41162746-41162746 + ATL178 COSM5707678 c.4471A>T p.T1491S Substitution - Missense 22:41172517-41172517 + TCGA-A5-A0GH-01 COSM1034544 c.3560G>A p.R1187H Substitution - Missense 22:41158470-41158470 + H524 COSM318349 c.4508A>C p.Y1503S Substitution - Missense 22:41172554-41172554 + SBC7 COSM318354 c.3410G>T p.R1137L Substitution - Missense 22:41157317-41157317 + TCGA-A6-5659-01 COSM3694076 c.1282+1G>A p.? Unknown 22:41130004-41130004 + ESCC-F21 COSM5047351 c.3806+1G>A p.? Unknown 22:41164131-41164131 + DM43 COSM5608365 c.6537C>T p.F2179F Substitution - coding silent 22:41178248-41178248 + ATL012 COSM1034571 c.4933C>T p.R1645* Substitution - Nonsense 22:41176400-41176400 + 2141 COSM88778 c.1768G>C p.A590P Substitution - Missense 22:41140147-41140147 + BJAB COSM88792 c.4025+1G>A p.? Unknown 22:41168600-41168600 + S02-15015-TP COSM3153105 c.1777C>T p.P593S Substitution - Missense 22:41140156-41140156 + ATL359 COSM5707680 c.5048G>A p.C1683Y Substitution - Missense 22:41176515-41176515 + 1N64-VS-1T64 COSM4978064 c.4398G>C p.W1466C Substitution - Missense 22:41170517-41170517 + ESCC-F71 COSM5048404 c.6877C>A p.H2293N Substitution - Missense 22:41178588-41178588 + PD8936a COSM4385253 c.3635G>A p.S1212N Substitution - Missense 22:41160686-41160686 + Patu8902t COSM96424 c.4949C>A p.S1650Y Substitution - Missense 22:41176416-41176416 + P134 COSM5010152 c.3882A>G p.P1294P Substitution - coding silent 22:41168456-41168456 + 090-05-01TD COSM145369 c.5368T>G p.C1790G Substitution - Missense 22:41177079-41177079 + ATL334 COSM5707670 c.968delT p.M323fs*39 Deletion - Frameshift 22:41127548-41127548 + HCT15 COSM96511 c.3040G>T p.E1014* Substitution - Nonsense 22:41152248-41152248 + pfg068T COSM1566439 c.6964delC p.H2324fs*29 Deletion - Frameshift 22:41178675-41178675 + TL65 COSM5751997 c.5336_5337insT p.I1781fs*102 Insertion - Frameshift 22:41177047-41177048 + DM37 COSM5608362 c.323C>T p.A108V Substitution - Missense 22:41117415-41117415 + MCF7 COSM1682287 c.4066C>T p.R1356* Substitution - Nonsense 22:41168761-41168761 + ccRCC-66 COSM1659917 c.1608C>T p.A536A Substitution - coding silent 22:41135892-41135892 + OVCAR-5 COSM1682290 c.5346C>A p.C1782* Substitution - Nonsense 22:41177057-41177057 + B90 COSM254673 c.4561G>C p.E1521Q Substitution - Missense 22:41172607-41172607 + 1N53-VS-1T53 COSM4976918 c.4135C>T p.Q1379* Substitution - Nonsense 22:41168830-41168830 + 2432697 COSM5352290 c.? p.I1612V Substitution - Missense CHC798T COSM4958210 c.2109G>A p.M703I Substitution - Missense 22:41146794-41146794 + HCC090T COSM5810687 c.3213A>C p.E1071D Substitution - Missense 22:41155065-41155065 + B80-13 COSM254669 c.4662G>C p.K1554N Substitution - Missense 22:41173667-41173667 + ESCC-F27 COSM5047451 c.4527G>C p.W1509C Substitution - Missense 22:41172573-41172573 + 407 COSM1716512 c.4540G>A p.E1514K Substitution - Missense 22:41172586-41172586 + S07-16280-TP COSM4991525 c.1014C>T p.I338I Substitution - coding silent 22:41127594-41127594 + TCGA-C5-A7UH-01 COSM4856801 c.3709G>T p.D1237Y Substitution - Missense 22:41162760-41162760 + TCGA-D1-A17Q-01 COSM1034581 c.6950G>T p.R2317L Substitution - Missense 22:41178661-41178661 + TCGA-BH-A18U-01 COSM445040 c.18G>A p.V6V Substitution - coding silent 22:41093022-41093022 + TARGET-20-PAKTCX-09A-01D COSM5487160 c.3874+2T>A p.? Unknown 22:41166668-41166668 + LS174T COSM3153069 c.89G>T p.G30V Substitution - Missense 22:41093093-41093093 + TCGA-BR-4292-01 COSM4104435 c.4067G>A p.R1356Q Substitution - Missense 22:41168762-41168762 + TCGA-D1-A177-01 COSM1034521 c.1543G>T p.G515* Substitution - Nonsense 22:41135827-41135827 + TCGA-G4-6628-01 COSM1416495 c.5862C>T p.H1954H Substitution - coding silent 22:41177573-41177573 + TCGA-EE-A3AA-06 COSM3554882 c.1499C>T p.P500L Substitution - Missense 22:41131604-41131604 + 587332 COSM1034579 c.6892C>T p.Q2298* Substitution - Nonsense 22:41178603-41178603 + B82-Tumor COSM4004938 c.6762T>G p.G2254G Substitution - coding silent 22:41178473-41178473 + TCGA-B5-A11E-01 COSM1034536 c.3302C>T p.T1101I Substitution - Missense 22:41157209-41157209 + 2011-2270:2012-310-T COSM122851 c.4195G>A p.D1399N Substitution - Missense 22:41169525-41169525 + DLD1 COSM269098 c.2512C>T p.R838C Substitution - Missense 22:41149893-41149893 + DM51 COSM5608366 c.930C>T p.V310V Substitution - coding silent 22:41127510-41127510 + ATL017 COSM5707671 c.1022A>C p.Q341P Substitution - Missense 22:41127602-41127602 + PD9221a COSM5945460 c.4398G>A p.W1466* Substitution - Nonsense 22:41170517-41170517 + PD8571a COSM5945463 c.5455C>T p.Q1819* Substitution - Nonsense 22:41177166-41177166 + ESCC_BICR_051T COSM5444054 c.4576G>A p.E1526K Substitution - Missense 22:41172622-41172622 + PD6296a COSM4385265 c.6796_6798delCAG p.Q2268delQ Deletion - In frame 22:41178507-41178509 + 2984_T COSM3964352 c.4256T>C p.I1419T Substitution - Missense 22:41169586-41169586 + XHDG60C COSM4767796 c.3183T>A p.T1061T Substitution - coding silent 22:41155035-41155035 + 179 COSM1741518 c.2532_2533insT p.T845fs*64 Insertion - Frameshift 22:41149913-41149914 + TCGA-AP-A0LM-01 COSM1034540 c.3355G>A p.D1119N Substitution - Missense 22:41157262-41157262 + T55 COSM4681092 c.3798G>A p.W1266* Substitution - Nonsense 22:41164122-41164122 + TCGA-EK-A2PM-01 COSM4831595 c.3849G>T p.R1283S Substitution - Missense 22:41166641-41166641 + WSU-HN6 COSM4602491 c.6221T>C p.L2074P Substitution - Missense 22:41177932-41177932 + TCGA-CK-5913-01 COSM1416475 c.3416A>G p.Y1139C Substitution - Missense 22:41157323-41157323 + B24-Tumor COSM122851 c.4195G>A p.D1399N Substitution - Missense 22:41169525-41169525 + 60 COSM5762875 c.2091T>G p.S697R Substitution - Missense 22:41146776-41146776 + PD6954a COSM4385268 c.7114A>G p.M2372V Substitution - Missense 22:41178825-41178825 + m111 COSM4387473 c.4505C>T p.P1502L Substitution - Missense 22:41172551-41172551 + S12-11594-TP COSM4991532 c.4212C>T p.F1404F Substitution - coding silent 22:41169542-41169542 + SC_9008 COSM5554838 c.5579G>A p.G1860D Substitution - Missense 22:41177290-41177290 + 100912 COSM95844 c.1839G>C p.R613R Substitution - coding silent 22:41140218-41140218 + pfg068T COSM84765 c.3671+1G>A p.? Unknown 22:41160723-41160723 + TCGA-A3-3320-01 COSM1495213 c.4287-2A>T p.? Unknown 22:41170404-41170404 + PD6974a COSM88786 c.6523A>C p.M2175L Substitution - Missense 22:41178234-41178234 + RK108_C01 COSM1632622 c.3728+4A>C p.? Unknown 22:41162783-41162783 + Patient_2_Relapse COSM5415056 c.6163_6164insC p.L2055fs*18 Insertion - Frameshift 22:41177874-41177875 + DM101 COSM1721877 c.2524C>T p.P842S Substitution - Missense 22:41149905-41149905 + DM59 COSM5608369 c.7048G>C p.G2350R Substitution - Missense 22:41178759-41178759 + sysucc-880T COSM5463124 c.5486G>A p.R1829H Substitution - Missense 22:41177197-41177197 + TCGA-BS-A0UA-01 COSM187721 c.4886C>T p.A1629V Substitution - Missense 22:41176353-41176353 + PD6782a COSM4385246 c.2512C>A p.R838S Substitution - Missense 22:41149893-41149893 + PD8935a COSM4385267 c.7061C>T p.A2354V Substitution - Missense 22:41178772-41178772 + PD7715a COSM5944806 c.5009_5010insG p.C1670fs*3 Insertion - Frameshift 22:41176476-41176477 + TCGA-AX-A0J0-01 COSM1034513 c.746A>G p.N249S Substitution - Missense 22:41125880-41125880 + 430 COSM96419 c.4195G>T p.D1399Y Substitution - Missense 22:41169525-41169525 + 1N22-VS-1T22 COSM1661670 c.4519G>A p.D1507N Substitution - Missense 22:41172565-41172565 + MDA-MB-435S COSM96422 c.2480T>C p.L827P Substitution - Missense 22:41149861-41149861 + S10-44607-TP COSM4991529 c.3396C>T p.N1132N Substitution - coding silent 22:41157303-41157303 + TCGA-FU-A3HY-01 COSM4838629 c.4742C>T p.S1581L Substitution - Missense 22:41173747-41173747 + BD124T COSM5494220 c.5931_5932insT p.G1978fs*95 Insertion - Frameshift 22:41177642-41177643 + m30 COSM4387476 c.4540_4541GA>AT p.E1514I Substitution - Missense 22:41172586-41172587 + TCGA-B0-5098-01 COSM1495211 c.6597A>G p.P2199P Substitution - coding silent 22:41178308-41178308 + TCGA-D8-A1XZ-01 COSM1484261 c.980C>T p.A327V Substitution - Missense 22:41127560-41127560 + PD6100a COSM4385257 c.4145G>A p.G1382D Substitution - Missense 22:41168840-41168840 + PD6544a COSM4170086 c.6626_6637del12 p.N2209_Q2213>K Complex - deletion inframe 22:41178337-41178348 + TCGA-66-2763-01 COSM122851 c.4195G>A p.D1399N Substitution - Missense 22:41169525-41169525 + TCGA-B5-A11E-01 COSM1034530 c.2789C>T p.P930L Substitution - Missense 22:41150170-41150170 + TCGA-EE-A2MS-06 COSM3554890 c.4099G>T p.D1367Y Substitution - Missense 22:41168794-41168794 + P158 COSM5008576 c.2978A>G p.Q993R Substitution - Missense 22:41151993-41151993 + TCGA-DK-A2I6-01 COSM96419 c.4195G>T p.D1399Y Substitution - Missense 22:41169525-41169525 + TCGA-D3-A2JF-06 COSM88784 c.4879C>T p.R1627W Substitution - Missense 22:41176346-41176346 + SJTALL006 COSM305992 c.4916T>C p.L1639P Substitution - Missense 22:41176383-41176383 + TCGA-JX-A3Q0-01 COSM4824823 c.952C>G p.P318A Substitution - Missense 22:41127532-41127532 + 5_FL COSM220521 c.4399T>A p.Y1467N Substitution - Missense 22:41170518-41170518 + S00472 COSM317282 c.4453-3C>G p.? Unknown 22:41172496-41172496 + V9 COSM4387477 c.4724_4759del36 p.N1575_A1586del Deletion - In frame 22:41173729-41173764 + DM8 COSM5608371 c.5563C>T p.P1855S Substitution - Missense 22:41177274-41177274 + S02354 COSM727028 c.4241A>G p.Y1414C Substitution - Missense 22:41169571-41169571 + SH-102782 COSM5021106 c.678C>G p.G226G Substitution - coding silent 22:41117770-41117770 + B10 COSM254666 c.2620C>T p.Q874* Substitution - Nonsense 22:41150001-41150001 + LIM2405 COSM96442 c.4401_4402insA p.M1470fs*3 Insertion - Frameshift 22:41170520-41170521 + ESCC_111 COSM254672 c.4352A>T p.H1451L Substitution - Missense 22:41170471-41170471 + TCGA-EB-A5UN-06 COSM3554885 c.2393G>A p.S798N Substitution - Missense 22:41149774-41149774 + PD6077a COSM4385263 c.5635C>T p.P1879S Substitution - Missense 22:41177346-41177346 + ESCC_87 COSM5636718 c.2439delG p.S815fs*35 Deletion - Frameshift 22:41149820-41149820 + PD5725a COSM4385250 c.3127C>T p.Q1043* Substitution - Nonsense 22:41152335-41152335 + HT115 COSM3153131 c.3135G>T p.K1045N Substitution - Missense 22:41152343-41152343 + LS411 COSM3153235 c.6963_6964insC p.H2324fs*55 Insertion - Frameshift 22:41178674-41178675 + PD6110a COSM4385243 c.2297C>T p.P766L Substitution - Missense 22:41149093-41149093 + TCGA-HF-7132-01 COSM1416465 c.444G>A p.T148T Substitution - coding silent 22:41117536-41117536 + 1N44-VS-1T44 COSM727028 c.4241A>G p.Y1414C Substitution - Missense 22:41169571-41169571 + PD18149a COSM5783822 c.1101C>G p.P367P Substitution - coding silent 22:41127681-41127681 + TCGA-G4-6322-01 COSM3694077 c.1511G>T p.R504L Substitution - Missense 22:41131616-41131616 + TCGA-JX-A3Q0-01 COSM1308214 c.6754G>T p.E2252* Substitution - Nonsense 22:41178465-41178465 + RXF393 COSM1682286 c.2405C>T p.P802L Substitution - Missense 22:41149786-41149786 + 8066491 COSM3785676 c.211G>C p.V71L Substitution - Missense 22:41117303-41117303 + SUDHL8 COSM88791 c.4636delA p.N1547fs*17 Deletion - Frameshift 22:41173641-41173641 + TCGA-EX-A1H5-01 COSM122851 c.4195G>A p.D1399N Substitution - Missense 22:41169525-41169525 + MD-326 COSM122851 c.4195G>A p.D1399N Substitution - Missense 22:41169525-41169525 + HCA7 COSM1566439 c.6964delC p.H2324fs*29 Deletion - Frameshift 22:41178675-41178675 + PD8735a COSM4385234 c.394A>T p.T132S Substitution - Missense 22:41117486-41117486 + S12-22512-TP COSM1205371 c.1811G>A p.R604Q Substitution - Missense 22:41140190-41140190 + ESCC_42 COSM13867 c.4355C>T p.P1452L Substitution - Missense 22:41170474-41170474 + PD8934a COSM4385249 c.2761G>A p.A921T Substitution - Missense 22:41150142-41150142 + TCGA-BS-A0UJ-01 COSM1034577 c.6250T>G p.F2084V Substitution - Missense 22:41177961-41177961 + pfg127T COSM4753584 c.5380A>G p.K1794E Substitution - Missense 22:41177091-41177091 + P134 COSM4104434 c.3591-1G>T p.? Unknown 22:41160641-41160641 + HN_62652 COSM97816 c.4154G>T p.C1385F Substitution - Missense 22:41168849-41168849 + PD7017a COSM4385266 c.6866C>T p.A2289V Substitution - Missense 22:41178577-41178577 + ESCC-F71 COSM4833737 c.3807-1G>C p.? Unknown 22:41166598-41166598 + SNUH_G17_S1 COSM3681448 c.5412G>A p.P1804P Substitution - coding silent 22:41177123-41177123 + B80-4 COSM254670 c.6883C>A p.Q2295K Substitution - Missense 22:41178594-41178594 + TCGA-BG-A0RY-01 COSM1034511 c.181delA p.I61fs*55 Deletion - Frameshift 22:41117273-41117273 + Pat_59_B COSM5859460 c.5036C>T p.T1679I Substitution - Missense 22:41176503-41176503 + SKCO-1 COSM1721877 c.2524C>T p.P842S Substitution - Missense 22:41149905-41149905 + RKO COSM3153169 c.4402delA p.M1470fs*26 Deletion - Frameshift 22:41170521-41170521 + cSCCP1 COSM135925 c.4355C>A p.P1452H Substitution - Missense 22:41170474-41170474 + Pat_30_A COSM5859457 c.3294T>A p.D1098E Substitution - Missense 22:41157201-41157201 + S00833 COSM317284 c.4123G>C p.G1375R Substitution - Missense 22:41168818-41168818 + TCGA-AA-A01G-01 COSM299838 c.1145G>A p.C382Y Substitution - Missense 22:41127725-41127725 + m117 COSM4387472 c.4409T>C p.M1470T Substitution - Missense 22:41170528-41170528 + 06-24881 COSM220523 c.4492G>A p.A1498T Substitution - Missense 22:41172538-41172538 + DLBCL-PatientD COSM221269 c.1244T>C p.L415P Substitution - Missense 22:41129965-41129965 + 1524440 COSM96456 c.? p.P925L Substitution - Missense 2432697 COSM5352315 c.? p.M187L Substitution - Missense J11_T COSM1682288 c.4319C>T p.P1440L Substitution - Missense 22:41170438-41170438 + S01524 COSM318353 c.3358G>T p.D1120Y Substitution - Missense 22:41157265-41157265 + TCGA-G4-6628-01 COSM1416472 c.2845G>T p.G949* Substitution - Nonsense 22:41151860-41151860 + PD6310a COSM4385265 c.6796_6798delCAG p.Q2268delQ Deletion - In frame 22:41178507-41178509 + ATL316 COSM4385260 c.4585C>T p.R1529* Substitution - Nonsense 22:41172631-41172631 + TCGA-BR-8591-01 COSM4104432 c.2241G>A p.P747P Substitution - coding silent 22:41147946-41147946 + 424 COSM4432631 c.5958G>A p.P1986P Substitution - coding silent 22:41177669-41177669 + 446 COSM4300086 c.4455T>A p.D1485E Substitution - Missense 22:41172501-41172501 + PD6816a COSM4385264 c.6266C>G p.A2089G Substitution - Missense 22:41177977-41177977 + WSU-HN8 COSM4602618 c.1579C>T p.L527F Substitution - Missense 22:41135863-41135863 + CHC1055T COSM217240 c.1169T>G p.V390G Substitution - Missense 22:41129890-41129890 + TCGA-A8-A0A6-01 COSM3842765 c.5748A>C p.P1916P Substitution - coding silent 22:41177459-41177459 + 18 COSM5745498 c.4432C>T p.R1478C Substitution - Missense 22:41170551-41170551 + I2L-P27-Tumor-Biopsy COSM5366372 c.6912_6915delCAAT p.N2305fs*47 Deletion - Frameshift 22:41178623-41178626 + S10-47754-TP COSM4991528 c.3220C>T p.P1074S Substitution - Missense 22:41155072-41155072 + TCGA-EK-A3GK-01 COSM4854311 c.6643C>T p.Q2215* Substitution - Nonsense 22:41178354-41178354 + S02279 COSM5683741 c.4389_4397delGCAGGAATG p.Q1464_W1466delQEW Deletion - In frame 22:41170508-41170516 + ESCC-F103 COSM5046777 c.3604G>C p.E1202Q Substitution - Missense 22:41160655-41160655 + 1685504 COSM235738 c.3442_3447delGTCTTT p.V1148_F1149delVF Deletion - In frame 22:41157349-41157354 + T578 COSM317283 c.3857A>G p.N1286S Substitution - Missense 22:41166649-41166649 + Esp66 COSM1742634 c.4453-1G>C p.? Unknown 22:41172498-41172498 + 18D COSM1235225 c.6584A>G p.Q2195R Substitution - Missense 22:41178295-41178295 + PD6306a COSM4385265 c.6796_6798delCAG p.Q2268delQ Deletion - In frame 22:41178507-41178509 + CRC-09T COSM5452886 c.1155C>T p.G385G Substitution - coding silent 22:41127735-41127735 + S00-28455-TP COSM4991527 c.1535G>A p.S512N Substitution - Missense 22:41135819-41135819 + 587238 COSM1205367 c.5956C>G p.P1986A Substitution - Missense 22:41177667-41177667 + S02275 COSM5682854 c.1981G>A p.A661T Substitution - Missense 22:41141150-41141150 + PD7379a COSM4385236 c.748C>T p.P250S Substitution - Missense 22:41125882-41125882 + TCGA-B5-A0JY-01 COSM1034575 c.5842T>A p.F1948I Substitution - Missense 22:41177553-41177553 + PD7100a COSM4385735 c.1806_1807insA p.R603fs*14 Insertion - Frameshift 22:41140185-41140186 + 587316 COSM1205371 c.1811G>A p.R604Q Substitution - Missense 22:41140190-41140190 + ESCC-010T COSM122851 c.4195G>A p.D1399N Substitution - Missense 22:41169525-41169525 + HCC86T COSM1616489 c.726_729+1delTAAGG p.? Unknown 22:41117818-41117822 + NB2198T COSM1236625 c.2692C>T p.Q898* Substitution - Nonsense 22:41150073-41150073 + ccRCC-43 COSM1661669 c.419C>T p.T140I Substitution - Missense 22:41117511-41117511 + TCGA-CG-4441-01 COSM4104437 c.5209C>T p.R1737C Substitution - Missense 22:41176920-41176920 + PD6282a COSM4385248 c.2668A>C p.T890P Substitution - Missense 22:41150049-41150049 + 27_tFL COSM4171090 c.89G>A p.G30D Substitution - Missense 22:41093093-41093093 + C91 COSM4444866 c.4235C>T p.A1412V Substitution - Missense 22:41169565-41169565 + TCGA-18-3409-01 COSM727023 c.6489C>T p.P2163P Substitution - coding silent 22:41178200-41178200 + 2180 COSM88776 c.376A>G p.M126V Substitution - Missense 22:41117468-41117468 + HCT-15 COSM96511 c.3040G>T p.E1014* Substitution - Nonsense 22:41152248-41152248 + 1523819 COSM88777 c.1519A>G p.S507G Substitution - Missense 22:41131624-41131624 + MD-286 COSM302136 c.4400A>G p.Y1467C Substitution - Missense 22:41170519-41170519 + PTC-14C COSM4156324 c.1421C>A p.P474H Substitution - Missense 22:41131526-41131526 + LUAD_E00565 COSM389441 c.3900C>T p.T1300T Substitution - coding silent 22:41168474-41168474 + H524 COSM318350 c.3270T>A p.F1090L Substitution - Missense 22:41157177-41157177 + P13 COSM4767796 c.3183T>A p.T1061T Substitution - coding silent 22:41155035-41155035 + PD6780a COSM4385259 c.4316C>A p.P1439Q Substitution - Missense 22:41170435-41170435 + KM12 COSM3153235 c.6963_6964insC p.H2324fs*55 Insertion - Frameshift 22:41178674-41178675 + S01861 COSM5671280 c.3482G>T p.G1161V Substitution - Missense 22:41157389-41157389 + 1053T COSM5825439 c.5386T>G p.C1796G Substitution - Missense 22:41177097-41177097 + 2538113 COSM5944158 c.5873C>T p.P1958L Substitution - Missense 22:41177584-41177584 + SK-OV-3 COSM727028 c.4241A>G p.Y1414C Substitution - Missense 22:41169571-41169571 + LUAD-CHTN-MAD06-00668 COSM359759 c.3124G>A p.G1042R Substitution - Missense 22:41152332-41152332 + P100 COSM5009342 c.3354C>T p.V1118V Substitution - coding silent 22:41157261-41157261 + HN14PT COSM97816 c.4154G>T p.C1385F Substitution - Missense 22:41168849-41168849 + TCGA-21-5786-01 COSM122851 c.4195G>A p.D1399N Substitution - Missense 22:41169525-41169525 + CN-AML-32-T COSM5424838 c.3501+2T>A p.? Unknown 22:41157410-41157410 + ESCC_26 COSM5627109 c.1943G>T p.R648L Substitution - Missense 22:41141112-41141112 + 1938969 COSM1666681 c.1019A>T p.Q340L Substitution - Missense 22:41127599-41127599 + PT13 COSM5896459 c.2773C>T p.P925S Substitution - Missense 22:41150154-41150154 + PD3192a COSM1658789 c.3742_3743delAC p.T1248fs*15 Deletion - Frameshift 22:41164066-41164067 + 3N58-VS-3T58 COSM4984100 c.512C>T p.A171V Substitution - Missense 22:41117604-41117604 + PD10815a COSM5487677 c.3491G>A p.C1164Y Substitution - Missense 22:41157398-41157398 + HN_62672 COSM122851 c.4195G>A p.D1399N Substitution - Missense 22:41169525-41169525 + YUMOBER COSM4856715 c.4934G>A p.R1645Q Substitution - Missense 22:41176401-41176401 + PD6259a COSM4385265 c.6796_6798delCAG p.Q2268delQ Deletion - In frame 22:41178507-41178509 + TCGA-GJ-A6C0-01 COSM4929999 c.7131T>C p.A2377A Substitution - coding silent 22:41178842-41178842 + PD6218a COSM727028 c.4241A>G p.Y1414C Substitution - Missense 22:41169571-41169571 + COR-L279 COSM96426 c.1623-(43)del3 p.? Unknown T3225 COSM4681096 c.6644A>G p.Q2215R Substitution - Missense 22:41178355-41178355 + 66 COSM4169966 c.2686C>T p.Q896* Substitution - Nonsense 22:41150067-41150067 + SJRHB012 COSM4776416 c.6630_6643del14 p.F2211fs*86 Deletion - Frameshift 22:41178341-41178354 + YUKAT COSM5393735 c.3262G>A p.D1088N Substitution - Missense 22:41157169-41157169 + 288 COSM1308206 c.4154G>A p.C1385Y Substitution - Missense 22:41168849-41168849 + YUNEKI COSM4385237 c.764C>T p.S255L Substitution - Missense 22:41125898-41125898 + B80-8-Tumor COSM254671 c.193C>T p.Q65* Substitution - Nonsense 22:41117285-41117285 + RKO COSM3153084 c.871delA p.K292fs*25 Deletion - Frameshift 22:41126005-41126005 + TCGA-MY-A5BD-01 COSM4855466 c.2329G>A p.V777I Substitution - Missense 22:41149125-41149125 + TCGA-CU-A3KJ-01 COSM1308209 c.5217C>G p.I1739M Substitution - Missense 22:41176928-41176928 + WSU-HN6 COSM4602263 c.6019C>T p.Q2007* Substitution - Nonsense 22:41177730-41177730 + Patient_3_Relapse COSM88793 c.4617+1G>A p.? Unknown 22:41172664-41172664 + I2L-P7-Tumor-Organoid COSM5366624 c.2352G>A p.P784P Substitution - coding silent 22:41149148-41149148 + T3498 COSM4681088 c.1751T>C p.V584A Substitution - Missense 22:41137781-41137781 + PD8145a COSM5945452 c.673C>T p.Q225* Substitution - Nonsense 22:41117765-41117765 + 1964121 COSM88790 c.4408delA p.M1470fs*26 Deletion - Frameshift 22:41170527-41170527 + H748 COSM318351 c.3996C>T p.T1332T Substitution - coding silent 22:41168570-41168570 + TCGA-37-3783-01 COSM727034 c.769T>G p.Y257D Substitution - Missense 22:41125903-41125903 + LIM-2405 COSM96441 c.2779_2780insC p.T928fs*21 Insertion - Frameshift 22:41150160-41150161 + PD6930a COSM88786 c.6523A>C p.M2175L Substitution - Missense 22:41178234-41178234 + TCGA-DK-A1A5-01 COSM419538 c.4227G>C p.L1409F Substitution - Missense 22:41169557-41169557 + PD3185a COSM1658811 c.4880delG p.D1628fs*81 Deletion - Frameshift 22:41176347-41176347 + PD7120a COSM4385265 c.6796_6798delCAG p.Q2268delQ Deletion - In frame 22:41178507-41178509 + 5_tFL COSM4171093 c.4347T>G p.H1449Q Substitution - Missense 22:41170466-41170466 + TCGA-AA-A010-01 COSM280814 c.3641C>A p.S1214Y Substitution - Missense 22:41160692-41160692 + TCGA-CZ-4859-01 COSM479000 c.6643C>A p.Q2215K Substitution - Missense 22:41178354-41178354 + PD7045a COSM4385233 c.312G>A p.M104I Substitution - Missense 22:41117404-41117404 + pfg030T COSM4747060 c.7012_7014delCAC p.H2339delH Deletion - In frame 22:41178723-41178725 + I2L-P19Tb-Tumor-Organoid COSM5366488 c.454G>T p.G152C Substitution - Missense 22:41117546-41117546 + KYSE-510 COSM3153134 c.3240C>T p.D1080D Substitution - coding silent 22:41155092-41155092 + ATL419 COSM3153106 c.1781C>T p.T594M Substitution - Missense 22:41140160-41140160 + sysucc-1030T COSM5452326 c.2111C>T p.P704L Substitution - Missense 22:41146796-41146796 + TCGA-D5-5540-01 COSM1416477 c.3731T>G p.F1244C Substitution - Missense 22:41164055-41164055 + B80-13-Tumor COSM254669 c.4662G>C p.K1554N Substitution - Missense 22:41173667-41173667 + TCGA-D5-5540-01 COSM1416476 c.3729-2A>T p.? Unknown 22:41164051-41164051 + FL007 COSM220521 c.4399T>A p.Y1467N Substitution - Missense 22:41170518-41170518 + TCGA-BG-A0LX-01 COSM187721 c.4886C>T p.A1629V Substitution - Missense 22:41176353-41176353 + ME009T COSM224101 c.1927G>A p.E643K Substitution - Missense 22:41141096-41141096 + UMC11 COSM3153075 c.378G>T p.M126I Substitution - Missense 22:41117470-41117470 + TCGA-GD-A3OQ-01 COSM1308206 c.4154G>A p.C1385Y Substitution - Missense 22:41168849-41168849 + MedB-1 COSM1682287 c.4066C>T p.R1356* Substitution - Nonsense 22:41168761-41168761 + 11114 COSM5751555 c.6798_6800delGCA p.Q2268delQ Deletion - In frame 22:41178509-41178511 + TCGA-AA-A010-01 COSM88784 c.4879C>T p.R1627W Substitution - Missense 22:41176346-41176346 + AOCS-135-8-X COSM4137484 c.2092G>C p.V698L Substitution - Missense 22:41146777-41146777 + SJTALL006 COSM305992 c.4916T>C p.L1639P Substitution - Missense 22:41176383-41176383 + TCGA-AX-A0J0-01 COSM1034548 c.3810C>T p.F1270F Substitution - coding silent 22:41166602-41166602 + RK308_C01 COSM3740447 c.6922C>T p.R2308C Substitution - Missense 22:41178633-41178633 + 107542 COSM94191 c.1936G>C p.E646Q Substitution - Missense 22:41141105-41141105 + TCGA-CU-A3KJ-01 COSM1308210 c.5364C>G p.L1788L Substitution - coding silent 22:41177075-41177075 + TCGA-LP-A5U2-01 COSM4833737 c.3807-1G>C p.? Unknown 22:41166598-41166598 + 2292387 COSM4610704 c.4606G>A p.E1536K Substitution - Missense 22:41172652-41172652 + SCC-25 COSM4387478 c.6668A>C p.Q2223P Substitution - Missense 22:41178379-41178379 + SJTALL007 COSM306019 c.1879-1G>A p.? Unknown 22:41141047-41141047 + TCGA-AD-6889-01 COSM1416497 c.6772C>T p.Q2258* Substitution - Nonsense 22:41178483-41178483 + B89-10 COSM255053 c.4377_4388del12 p.P1460_L1463delPKRL Deletion - In frame 22:41170496-41170507 + 2024537 COSM1716512 c.4540G>A p.E1514K Substitution - Missense 22:41172586-41172586 + TCGA-BH-A0HF-01 COSM3842759 c.1349C>T p.A450V Substitution - Missense 22:41131454-41131454 + 745_T COSM3964349 c.2132-2A>G p.? Unknown 22:41147835-41147835 + L02 COSM220522 c.4399T>C p.Y1467H Substitution - Missense 22:41170518-41170518 + TCGA-CU-A3KJ-01 COSM1034571 c.4933C>T p.R1645* Substitution - Nonsense 22:41176400-41176400 + J76_T COSM3964350 c.2830G>T p.A944S Substitution - Missense 22:41151845-41151845 + HCT116 COSM96433 c.5095delA p.N1700fs*9 Deletion - Frameshift 22:41176806-41176806 + KM12 COSM1682285 c.2282A>G p.Q761R Substitution - Missense 22:41149078-41149078 + SUDHL10 COSM88783 c.4796G>A p.R1599H Substitution - Missense 22:41176263-41176263 + 2161 COSM88777 c.1519A>G p.S507G Substitution - Missense 22:41131624-41131624 + PD5779a COSM4385265 c.6796_6798delCAG p.Q2268delQ Deletion - In frame 22:41178507-41178509 + SW48 COSM3153106 c.1781C>T p.T594M Substitution - Missense 22:41140160-41140160 + 2_RESISTANT COSM1721877 c.2524C>T p.P842S Substitution - Missense 22:41149905-41149905 + TCGA-D1-A0ZR-01 COSM1034566 c.4467_4468insG p.A1490fs*3 Insertion - Frameshift 22:41172513-41172514 + 1964030 COSM88790 c.4408delA p.M1470fs*26 Deletion - Frameshift 22:41170527-41170527 + TCGA-BR-6852-01 COSM274975 c.1739G>A p.R580Q Substitution - Missense 22:41137769-41137769 + ccRCC-52 COSM1661670 c.4519G>A p.D1507N Substitution - Missense 22:41172565-41172565 + TCGA-IR-A3LK-01 COSM4818071 c.842C>G p.S281* Substitution - Nonsense 22:41125976-41125976 + HT115 COSM4612692 c.4564_4565insTGGAAG p.Q1522>LEE Complex - insertion inframe 22:41172610-41172611 + TCGA-A5-A0GH-01 COSM1034558 c.4048G>A p.A1350T Substitution - Missense 22:41168743-41168743 + OVCAR-8 COSM96513 c.5188delT p.S1730fs*4 Deletion - Frameshift 22:41176899-41176899 + 2523559 COSM5881455 c.? p.M1470fs*2 Frameshift PD6918a COSM4385240 c.1442C>A p.P481Q Substitution - Missense 22:41131547-41131547 + PD6822a COSM4385245 c.2456G>A p.C819Y Substitution - Missense 22:41149837-41149837 + 3N24-VS-3T24 COSM4979790 c.4065C>G p.Y1355* Substitution - Nonsense 22:41168760-41168760 + 2321369 COSM122851 c.4195G>A p.D1399N Substitution - Missense 22:41169525-41169525 + OSCC-GB_00600111 COSM122851 c.4195G>A p.D1399N Substitution - Missense 22:41169525-41169525 + ATL271 COSM96442 c.4401_4402insA p.M1470fs*3 Insertion - Frameshift 22:41170520-41170521 + S10-47754-TP COSM4991534 c.4511T>C p.F1504S Substitution - Missense 22:41172557-41172557 + ATL065 COSM5707676 c.2061_2077del17 p.L688fs*105 Deletion - Frameshift 22:41146746-41146762 + 1964029 COSM88790 c.4408delA p.M1470fs*26 Deletion - Frameshift 22:41170527-41170527 + PD7728a COSM3153139 c.3602G>A p.C1201Y Substitution - Missense 22:41160653-41160653 + VP229 COSM96433 c.5095delA p.N1700fs*9 Deletion - Frameshift 22:41176806-41176806 + TCGA-AA-A010-01 COSM280813 c.251T>C p.L84S Substitution - Missense 22:41117343-41117343 + 1964122 COSM1651571 c.6970_6971insC p.H2324fs*55 Insertion - Frameshift 22:41178681-41178682 + SNB75 COSM1683282 c.5860_5861insTTG p.H1954>LD Complex - insertion inframe 22:41177571-41177572 + PD4983a COSM5778419 c.6418G>A p.V2140I Substitution - Missense 22:41178129-41178129 + 2432698 COSM5352293 c.? p.A2354T Substitution - Missense GHE0609 COSM5714191 c.1741A>C p.N581H Substitution - Missense 22:41137771-41137771 + TCGA-A8-A0A7-01 COSM445041 c.2299C>T p.Q767* Substitution - Nonsense 22:41149095-41149095 + 587220 COSM1205368 c.2921A>G p.Q974R Substitution - Missense 22:41151936-41151936 + ID32 COSM1166774 c.5056_5057delTG p.C1686fs*1 Deletion - Frameshift 22:41176523-41176524 + 2217109 COSM4169403 c.? p.R604Q Substitution - Missense STC291 COSM3153115 c.2182C>T p.R728W Substitution - Missense 22:41147887-41147887 + 2321297 COSM4774860 c.5109C>T p.H1703H Substitution - coding silent 22:41176820-41176820 + PDA_009 COSM4998369 c.1470C>A p.N490K Substitution - Missense 22:41131575-41131575 + 2011-2260:2012-1319-T COSM4605375 c.4368G>C p.K1456N Substitution - Missense 22:41170487-41170487 + 1645947 COSM150918 c.5030_5036delTGGAGAC p.V1677fs*30 Deletion - Frameshift 22:41176497-41176503 + TCGA-BH-A18G-01 COSM3153169 c.4402delA p.M1470fs*26 Deletion - Frameshift 22:41170521-41170521 + B106-Tumor COSM254667 c.4454A>T p.D1485V Substitution - Missense 22:41172500-41172500 + 2432698 COSM5352315 c.? p.M187L Substitution - Missense TCGA-D8-A1XM-01 COSM1484263 c.2498C>T p.S833L Substitution - Missense 22:41149879-41149879 + V278 COSM4387468 c.4115G>A p.C1372Y Substitution - Missense 22:41168810-41168810 + 5_tFL COSM4171094 c.4448A>G p.Y1483C Substitution - Missense 22:41170567-41170567 + PD13775a COSM5024941 c.6284C>G p.S2095C Substitution - Missense 22:41177995-41177995 + B89-4-Tumor COSM254672 c.4352A>T p.H1451L Substitution - Missense 22:41170471-41170471 + TCGA-BG-A0MG-01 COSM1034573 c.5014G>T p.E1672* Substitution - Nonsense 22:41176481-41176481 + EGC28 COSM4833752 c.2855C>G p.S952* Substitution - Nonsense 22:41151870-41151870 + sysucc-1370T COSM5471518 c.5185G>A p.D1729N Substitution - Missense 22:41176896-41176896 + B80-4 COSM254670 c.6883C>A p.Q2295K Substitution - Missense 22:41178594-41178594 + RH30SJ_ COSM3153122 c.2671A>C p.T891P Substitution - Missense 22:41150052-41150052 + LUAD-D02085 COSM363359 c.4880G>A p.R1627Q Substitution - Missense 22:41176347-41176347 + TCGA-BR-4184-01 COSM4104426 c.20A>G p.E7G Substitution - Missense 22:41093024-41093024 + T1154 COSM4681087 c.1369A>G p.S457G Substitution - Missense 22:41131474-41131474 + ESCC_24 COSM4387470 c.4343T>C p.F1448S Substitution - Missense 22:41170462-41170462 + DLD1 COSM96511 c.3040G>T p.E1014* Substitution - Nonsense 22:41152248-41152248 + P134 COSM187721 c.4886C>T p.A1629V Substitution - Missense 22:41176353-41176353 + PT45 COSM5927911 c.1246C>T p.P416S Substitution - Missense 22:41129967-41129967 + SH-7329 COSM5020743 c.7177C>G p.L2393V Substitution - Missense 22:41178888-41178888 + TCGA-BR-8381-01 COSM4104436 c.4388T>G p.L1463R Substitution - Missense 22:41170507-41170507 + Gp5D COSM3153094 c.1268A>C p.K423T Substitution - Missense 22:41129989-41129989 + TCGA-FD-A3SM-01 COSM3800225 c.3667C>G p.Q1223E Substitution - Missense 22:41160718-41160718 + CSCC-47-T COSM4387473 c.4505C>T p.P1502L Substitution - Missense 22:41172551-41172551 + TCGA-EA-A3HQ-01 COSM4843126 c.1942C>T p.R648* Substitution - Nonsense 22:41141111-41141111 + HCC060T COSM5818110 c.3052G>T p.E1018* Substitution - Nonsense 22:41152260-41152260 + cSCCP11 COSM143785 c.? p.Q974* Substitution - Nonsense B78 COSM254668 c.2470C>T p.Q824* Substitution - Nonsense 22:41149851-41149851 + RK217_C01 COSM88793 c.4617+1G>A p.? Unknown 22:41172664-41172664 + P04-2666 COSM244264 c.6802C>A p.Q2268K Substitution - Missense 22:41178513-41178513 + TCGA-BR-8382-01 COSM1205369 c.4397G>T p.W1466L Substitution - Missense 22:41170516-41170516 + 2321342 COSM4775084 c.7219T>C p.S2407P Substitution - Missense 22:41178930-41178930 + P100 COSM5009341 c.260C>A p.S87Y Substitution - Missense 22:41117352-41117352 + T3225 COSM4681091 c.3603T>C p.C1201C Substitution - coding silent 22:41160654-41160654 + TCGA-EK-A2R8-01 COSM4300068 c.1681C>T p.Q561* Substitution - Nonsense 22:41137711-41137711 + TCGA-FU-A3TQ-01 COSM84765 c.3671+1G>A p.? Unknown 22:41160723-41160723 + PD4116a COSM219544 c.2957A>T p.Q986L Substitution - Missense 22:41151972-41151972 + ATL237 COSM3153146 c.3701_3702insA p.N1236fs*2 Insertion - Frameshift 22:41162752-41162753 + 2432710 COSM5352298 c.? p.R838C Substitution - Missense ESCC-216T COSM96419 c.4195G>T p.D1399Y Substitution - Missense 22:41169525-41169525 + PD7010a COSM4385262 c.4714G>A p.G1572R Substitution - Missense 22:41173719-41173719 + ESO-143 COSM1251229 c.1636G>A p.E546K Substitution - Missense 22:41137666-41137666 + Pat_40_B COSM5859462 c.5833G>A p.V1945M Substitution - Missense 22:41177544-41177544 + V53 COSM727028 c.4241A>G p.Y1414C Substitution - Missense 22:41169571-41169571 + HCT116 COSM3153169 c.4402delA p.M1470fs*26 Deletion - Frameshift 22:41170521-41170521 + PD10895a COSM4849197 c.5155C>T p.Q1719* Substitution - Nonsense 22:41176866-41176866 + Pat_45_B COSM5859456 c.3260C>T p.P1087L Substitution - Missense 22:41155112-41155112 + B87 COSM255072 c.4239_4240insT p.Y1414fs*3 Insertion - Frameshift 22:41169569-41169570 + TCGA-BG-A0MU-01 COSM1034542 c.3377A>G p.N1126S Substitution - Missense 22:41157284-41157284 + TCGA-36-2542-01 COSM1327208 c.1906A>G p.K636E Substitution - Missense 22:41141075-41141075 + PD6272a COSM4385251 c.3256A>G p.I1086V Substitution - Missense 22:41155108-41155108 + TCGA-A7-A4SA-01 COSM3842763 c.4915C>T p.L1639L Substitution - coding silent 22:41176382-41176382 + YUWAPO COSM5393734 c.1378G>T p.D460Y Substitution - Missense 22:41131483-41131483 + PD8405a COSM5945458 c.3601T>C p.C1201R Substitution - Missense 22:41160652-41160652 + S02344 COSM88793 c.4617+1G>A p.? Unknown 22:41172664-41172664 + FL14 COSM88786 c.6523A>C p.M2175L Substitution - Missense 22:41178234-41178234 + TCGA-EE-A2GL-06 COSM3554892 c.5482C>T p.L1828F Substitution - Missense 22:41177193-41177193 + 2011-2314:2012-359-T COSM4605782 c.6820C>T p.Q2274* Substitution - Nonsense 22:41178531-41178531 + YULAN COSM1714420 c.2590C>T p.P864S Substitution - Missense 22:41149971-41149971 + S02209 COSM1682288 c.4319C>T p.P1440L Substitution - Missense 22:41170438-41170438 + HCC105T COSM1034534 c.3117G>A p.P1039P Substitution - coding silent 22:41152325-41152325 + ESCC_BICR_051T COSM1284744 c.2743C>T p.R915C Substitution - Missense 22:41150124-41150124 + TCGA-G2-A2EJ-01 COSM1308203 c.2245A>G p.M749V Substitution - Missense 22:41149041-41149041 + 49_tFL COSM4171091 c.787C>G p.Q263E Substitution - Missense 22:41125921-41125921 + CHC798T COSM4958210 c.2109G>A p.M703I Substitution - Missense 22:41146794-41146794 + 469 COSM96419 c.4195G>T p.D1399Y Substitution - Missense 22:41169525-41169525 + B80-13 COSM254669 c.4662G>C p.K1554N Substitution - Missense 22:41173667-41173667 + 2432695 COSM5352289 c.? p.T594M Substitution - Missense 2011-2340:2012-304-T COSM4603808 c.4340_4342delTCT p.F1448delF Deletion - In frame 22:41170459-41170461 + S02296 COSM5701415 c.2024_2025insT p.M675fs*11 Insertion - Frameshift 22:41141193-41141194 + Gp2D COSM3153094 c.1268A>C p.K423T Substitution - Missense 22:41129989-41129989 + RKO COSM3153153 c.3927T>C p.F1309F Substitution - coding silent 22:41168501-41168501 + 20 COSM4169964 c.6776C>T p.A2259V Substitution - Missense 22:41178487-41178487 + ATL014 COSM5575223 c.5006C>T p.T1669I Substitution - Missense 22:41176473-41176473 + TCGA-KK-A59V-01 COSM4878676 c.6229A>G p.N2077D Substitution - Missense 22:41177940-41177940 + S04-6933-TP COSM4991537 c.6950G>A p.R2317Q Substitution - Missense 22:41178661-41178661 + B86 COSM88784 c.4879C>T p.R1627W Substitution - Missense 22:41176346-41176346 + SW620 COSM1682288 c.4319C>T p.P1440L Substitution - Missense 22:41170438-41170438 + TCGA-E9-A1N3-01 COSM1484262 c.1501_1502insG p.Q501fs*12 Insertion - Frameshift 22:41131606-41131607 + TCGA-EE-A2GO-06 COSM3554894 c.5947G>A p.G1983R Substitution - Missense 22:41177658-41177658 + 66 COSM4169965 c.4863C>A p.C1621* Substitution - Nonsense 22:41176330-41176330 + PD6496a COSM4385239 c.1081G>A p.V361M Substitution - Missense 22:41127661-41127661 + 389 COSM4427680 c.1667_1668insT p.M556fs*61 Insertion - Frameshift 22:41137697-41137698 + TCGA-JX-A3Q0-01 COSM4824049 c.2221C>T p.Q741* Substitution - Nonsense 22:41147926-41147926 + TCGA-LP-A5U2-01 COSM4833752 c.2855C>G p.S952* Substitution - Nonsense 22:41151870-41151870 + B90-Tumor COSM254673 c.4561G>C p.E1521Q Substitution - Missense 22:41172607-41172607 + SH-3776 COSM4387478 c.6668A>C p.Q2223P Substitution - Missense 22:41178379-41178379 + TCGA-AA-A00N-01 COSM274975 c.1739G>A p.R580Q Substitution - Missense 22:41137769-41137769 + TCGA-EI-6917-01 COSM274975 c.1739G>A p.R580Q Substitution - Missense 22:41137769-41137769 + 38T COSM3153139 c.3602G>A p.C1201Y Substitution - Missense 22:41160653-41160653 + B106 COSM254667 c.4454A>T p.D1485V Substitution - Missense 22:41172500-41172500 + P9 COSM5009621 c.2989A>G p.I997V Substitution - Missense 22:41152004-41152004 + 1658 COSM88793 c.4617+1G>A p.? Unknown 22:41172664-41172664 + HCT8 COSM4634806 c.5791C>T p.Q1931* Substitution - Nonsense 22:41177502-41177502 + S00-35182-TP COSM4991533 c.4213C>T p.R1405C Substitution - Missense 22:41169543-41169543 + Pat_28_B COSM5859451 c.335G>A p.S112N Substitution - Missense 22:41117427-41117427 + MATU COSM96430 c.3591_3728del138 p.Y1198_L1243del Deletion - In frame 22:41160642-41162779 + TCGA-BR-8372-01 COSM1205369 c.4397G>T p.W1466L Substitution - Missense 22:41170516-41170516 + TCGA-EE-A29D-06 COSM3554895 c.6160C>T p.L2054F Substitution - Missense 22:41177871-41177871 + TCGA-A6-6780-01 COSM1416492 c.5485C>T p.R1829C Substitution - Missense 22:41177196-41177196 + LC_S42 COSM1190460 c.4955T>C p.M1652T Substitution - Missense 22:41176422-41176422 + 2432710 COSM5352297 c.? p.R568W Substitution - Missense TCGA-CA-5796-01 COSM1416470 c.1784C>T p.P595L Substitution - Missense 22:41140163-41140163 + ESCC_50 COSM1682288 c.4319C>T p.P1440L Substitution - Missense 22:41170438-41170438 + PT19_2 COSM5900429 c.6628C>T p.Q2210* Substitution - Nonsense 22:41178339-41178339 + V208 COSM4387474 c.4534_4536delGTT p.V1512del Deletion - In frame 22:41172580-41172582 + 46M COSM5587723 c.183T>C p.I61I Substitution - coding silent 22:41117275-41117275 + PD6082a COSM4385237 c.764C>T p.S255L Substitution - Missense 22:41125898-41125898 + 2321295 COSM4774847 c.5358_5359insA p.A1787fs*96 Insertion - Frameshift 22:41177069-41177070 + PD7373a COSM3153139 c.3602G>A p.C1201Y Substitution - Missense 22:41160653-41160653 + LUAD-YINHD COSM350324 c.4391A>T p.Q1464L Substitution - Missense 22:41170510-41170510 + T2197 COSM4681093 c.4382A>G p.K1461R Substitution - Missense 22:41170501-41170501 + LS180 COSM3153069 c.89G>T p.G30V Substitution - Missense 22:41093093-41093093 + TCGA-CG-4442-01 COSM4104444 c.7102G>A p.D2368N Substitution - Missense 22:41178813-41178813 + PD6250a COSM4385265 c.6796_6798delCAG p.Q2268delQ Deletion - In frame 22:41178507-41178509 + PT37 COSM5921846 c.2296C>T p.P766S Substitution - Missense 22:41149092-41149092 + TCGA-AA-3869-01 COSM296222 c.6819T>G p.V2273V Substitution - coding silent 22:41178530-41178530 + LUAD-CHTN-MAD06-00668 COSM359758 c.2707G>T p.A903S Substitution - Missense 22:41150088-41150088 + ESCC-F42 COSM5047782 c.1465A>T p.K489* Substitution - Nonsense 22:41131570-41131570 + CSCC-40-T COSM727023 c.6489C>T p.P2163P Substitution - coding silent 22:41178200-41178200 + LB771-HNC COSM13867 c.4355C>T p.P1452L Substitution - Missense 22:41170474-41170474 + PD8621a COSM5789312 c.4228A>T p.R1410W Substitution - Missense 22:41169558-41169558 + PD13775a COSM5024942 c.7121C>T p.S2374F Substitution - Missense 22:41178832-41178832 + SUM-149 COSM96429 c.4025+(28)del3 p.? Unknown 2432698 COSM5352316 c.? p.R1599H Substitution - Missense TARGET-20-PARCVS-04A-01D COSM5487620 c.3805G>T p.G1269* Substitution - Nonsense 22:41164129-41164129 + ESCC_BICR_005T COSM5439144 c.4076C>T p.A1359V Substitution - Missense 22:41168771-41168771 + PD11085a COSM5945461 c.4453-2A>T p.? Unknown 22:41172497-41172497 + PD8095a COSM5944414 c.6567_6571delGCAAC p.M2189fs*19 Deletion - Frameshift 22:41178278-41178282 + TCGA-26-6173-01 COSM3153139 c.3602G>A p.C1201Y Substitution - Missense 22:41160653-41160653 + 12_tFL COSM4171092 c.2003C>T p.S668F Substitution - Missense 22:41141172-41141172 + YUWAND COSM1714419 c.1551T>A p.N517K Substitution - Missense 22:41135835-41135835 + TCGA-B8-5158-01 COSM479001 c.7079A>G p.E2360G Substitution - Missense 22:41178790-41178790 + CN-AML-NR-13-Dx COSM5424838 c.3501+2T>A p.? Unknown 22:41157410-41157410 + P9 COSM96442 c.4401_4402insA p.M1470fs*3 Insertion - Frameshift 22:41170520-41170521 + CLL033 COSM1291254 c.2840T>C p.I947T Substitution - Missense 22:41151855-41151855 + TCGA-FU-A3HZ-01 COSM3153099 c.1443G>A p.P481P Substitution - coding silent 22:41131548-41131548 + m39 COSM4387471 c.4365G>T p.Q1455H Substitution - Missense 22:41170484-41170484 + TCGA-18-3419-01 COSM727030 c.4173-2A>G p.? Unknown 22:41169501-41169501 + PD6114a COSM4385254 c.3659C>G p.S1220C Substitution - Missense 22:41160710-41160710 + DM42 COSM4171092 c.2003C>T p.S668F Substitution - Missense 22:41141172-41141172 + 2432704 COSM5352294 c.? p.R353C Substitution - Missense KYSE110 COSM5049517 c.4858C>T p.P1620S Substitution - Missense 22:41176325-41176325 + EGC15 COSM5057844 c.1880C>T p.A627V Substitution - Missense 22:41141049-41141049 + T3668 COSM3153146 c.3701_3702insA p.N1236fs*2 Insertion - Frameshift 22:41162752-41162753 + PD6329a COSM4385235 c.533T>A p.L178* Substitution - Nonsense 22:41117625-41117625 + OSCC-GB_00870111 COSM96419 c.4195G>T p.D1399Y Substitution - Missense 22:41169525-41169525 + PD4116a COSM219544 c.2957A>T p.Q986L Substitution - Missense 22:41151972-41151972 + HCC2998 COSM1682284 c.1393G>T p.E465* Substitution - Nonsense 22:41131498-41131498 + TCGA-JW-A852-01 COSM122851 c.4195G>A p.D1399N Substitution - Missense 22:41169525-41169525 + RK308_C01 COSM3740444 c.1303G>A p.V435I Substitution - Missense 22:41131408-41131408 + PD4200a COSM160791 c.1854C>G p.D618E Substitution - Missense 22:41140233-41140233 + 2492729 COSM5726504 c.1462G>A p.A488T Substitution - Missense 22:41131567-41131567 + FL1 COSM88780 c.4189T>C p.Y1397H Substitution - Missense 22:41169519-41169519 + Gp5D COSM3153189 c.4981C>T p.Q1661* Substitution - Nonsense 22:41176448-41176448 + P129 COSM5009621 c.2989A>G p.I997V Substitution - Missense 22:41152004-41152004 + I2L-P19Tb-Tumor-Biopsy COSM5366485 c.4351C>A p.H1451N Substitution - Missense 22:41170470-41170470 + B87 COSM255072 c.4239_4240insT p.Y1414fs*3 Insertion - Frameshift 22:41169569-41169570 + TCGA-BR-4184-01 COSM4104441 c.6616G>T p.A2206S Substitution - Missense 22:41178327-41178327 + PD4127a COSM160790 c.2090G>A p.S697N Substitution - Missense 22:41146775-41146775 + SC-her2-043 COSM4777522 c.4198A>G p.S1400G Substitution - Missense 22:41169528-41169528 + DM10 COSM5608359 c.4515G>T p.E1505D Substitution - Missense 22:41172561-41172561 + TCGA-BS-A0TJ-01 COSM1034524 c.1778C>A p.P593H Substitution - Missense 22:41140157-41140157 + PLK106Ca COSM96420 c.5038C>T p.R1680C Substitution - Missense 22:41176505-41176505 + OSCC-GB_00180111 COSM3713703 c.6856C>A p.P2286T Substitution - Missense 22:41178567-41178567 + Pat_26_B COSM5859453 c.1561_1562GG>AA p.G521K Substitution - Missense 22:41135845-41135846 + SC-her2-046 COSM320129 c.5189C>T p.S1730F Substitution - Missense 22:41176900-41176900 + ATLL_A-01 COSM5575223 c.5006C>T p.T1669I Substitution - Missense 22:41176473-41176473 + BrCa8 COSM96435 c.(4025)ins18 p.(1409)ins6 Insertion - In frame tumor_4158726 COSM3357343 c.4312T>C p.C1438R Substitution - Missense 22:41170431-41170431 + PLK848Ca COSM96419 c.4195G>T p.D1399Y Substitution - Missense 22:41169525-41169525 + Pat_24_A COSM5859461 c.5057G>A p.C1686Y Substitution - Missense 22:41176524-41176524 + HCT-116 COSM96433 c.5095delA p.N1700fs*9 Deletion - Frameshift 22:41176806-41176806 + T3658 COSM4681094 c.5810A>G p.E1937G Substitution - Missense 22:41177521-41177521 + Gp2D COSM4628039 c.6117C>T p.S2039S Substitution - coding silent 22:41177828-41177828 + P129 COSM4767796 c.3183T>A p.T1061T Substitution - coding silent 22:41155035-41155035 + Pa03C COSM84765 c.3671+1G>A p.? Unknown 22:41160723-41160723 + RK200_C01 COSM3740445 c.4301A>G p.H1434R Substitution - Missense 22:41170420-41170420 + NCI-ADR-RES COSM96513 c.5188delT p.S1730fs*4 Deletion - Frameshift 22:41176899-41176899 + B80-8 COSM254671 c.193C>T p.Q65* Substitution - Nonsense 22:41117285-41117285 + B78-Tumor COSM254668 c.2470C>T p.Q824* Substitution - Nonsense 22:41149851-41149851 + ATL294 COSM254668 c.2470C>T p.Q824* Substitution - Nonsense 22:41149851-41149851 + TCGA-B5-A11E-01 COSM1034552 c.3842G>A p.R1281Q Substitution - Missense 22:41166634-41166634 + 2432698 COSM5352292 c.? p.R705Q Substitution - Missense 2432710 COSM5352299 c.? p.M1157I Substitution - Missense S08-7608-TP COSM4991530 c.3619G>T p.E1207* Substitution - Nonsense 22:41160670-41160670 + HCC2998 COSM1682289 c.4751T>G p.L1584R Substitution - Missense 22:41173756-41173756 + 2334191 COSM320130 c.4114T>C p.C1372R Substitution - Missense 22:41168809-41168809 + TCGA-AP-A056-01 COSM1034532 c.2820T>G p.L940L Substitution - coding silent 22:41151835-41151835 + SC-her2-046 COSM4943269 c.7138C>G p.P2380A Substitution - Missense 22:41178849-41178849 + DM36 COSM5611262 c.2639_2641CCC>TTT p.P880_P881>LS Complex - compound substitution 22:41150020-41150022 + ccRCC-95 COSM1660059 c.1138A>G p.T380A Substitution - Missense 22:41127718-41127718 + TCGA-EB-A41A-01 COSM88785 c.5711A>C p.Q1904P Substitution - Missense 22:41177422-41177422 + S03-45671-TP COSM4991524 c.961C>T p.Q321* Substitution - Nonsense 22:41127541-41127541 + DB COSM88781 c.4517G>T p.G1506V Substitution - Missense 22:41172563-41172563 + 403 COSM320130 c.4114T>C p.C1372R Substitution - Missense 22:41168809-41168809 + H1836 COSM318348 c.4186T>C p.S1396P Substitution - Missense 22:41169516-41169516 + T3724 COSM3153235 c.6963_6964insC p.H2324fs*55 Insertion - Frameshift 22:41178674-41178675 + PD8046a COSM5944413 c.5618_5622delCTCAG p.Q1874fs*7 Deletion - Frameshift 22:41177329-41177333 + TCGA-37-3783-01 COSM727028 c.4241A>G p.Y1414C Substitution - Missense 22:41169571-41169571 + SH-102782 COSM5021083 c.4311A>C p.A1437A Substitution - coding silent 22:41170430-41170430 + 090-02-1TD COSM145369 c.5368T>G p.C1790G Substitution - Missense 22:41177079-41177079 + TCGA-BR-4201-01 COSM4104427 c.620A>G p.Y207C Substitution - Missense 22:41117712-41117712 + HCT116 COSM96442 c.4401_4402insA p.M1470fs*3 Insertion - Frameshift 22:41170520-41170521 + TCGA-G2-A2EL-01 COSM1308207 c.4365G>C p.Q1455H Substitution - Missense 22:41170484-41170484 + TCGA-EI-6917-01 COSM3424203 c.4864G>A p.D1622N Substitution - Missense 22:41176331-41176331 + TCGA-BH-A18G-01 COSM3842766 c.5854A>G p.I1952V Substitution - Missense 22:41177565-41177565 + B78 COSM254668 c.2470C>T p.Q824* Substitution - Nonsense 22:41149851-41149851 + CoCa6 COSM96421 c.1738C>T p.R580* Substitution - Nonsense 22:41137768-41137768 + 1964123 COSM1651571 c.6970_6971insC p.H2324fs*55 Insertion - Frameshift 22:41178681-41178682 + PD6514a COSM4385265 c.6796_6798delCAG p.Q2268delQ Deletion - In frame 22:41178507-41178509 + P9 COSM5009882 c.2240C>T p.P747L Substitution - Missense 22:41147945-41147945 + TCGA-EE-A2A6-06 COSM3554884 c.1897C>T p.L633L Substitution - coding silent 22:41141066-41141066 + 2321297 COSM4774852 c.3667C>T p.Q1223* Substitution - Nonsense 22:41160718-41160718 + PD11285a COSM5945455 c.2997+5G>A p.? Unknown 22:41152017-41152017 + LB647-SCLC COSM27189 c.5850G>T p.R1950S Substitution - Missense 22:41177561-41177561 + ESO-859 COSM1238789 c.5587C>T p.P1863S Substitution - Missense 22:41177298-41177298 + CHC2141T COSM4790209 c.5638C>A p.P1880T Substitution - Missense 22:41177349-41177349 + TCGA-60-2713-01 COSM727026 c.5633C>A p.T1878N Substitution - Missense 22:41177344-41177344 + PD6987a COSM4385265 c.6796_6798delCAG p.Q2268delQ Deletion - In frame 22:41178507-41178509 + 389 COSM4427681 c.5599C>A p.Q1867K Substitution - Missense 22:41177310-41177310 + Pa16C COSM85623 c.4461_4462insT p.K1488fs*1 Insertion - Frameshift 22:41172507-41172508 + OSCC-GB_00340111 COSM3713737 c.511G>T p.A171S Substitution - Missense 22:41117603-41117603 + TCGA-GM-A2DL-01 COSM3842758 c.775C>T p.Q259* Substitution - Nonsense 22:41125909-41125909 + 416 COSM727028 c.4241A>G p.Y1414C Substitution - Missense 22:41169571-41169571 + 2025 COSM88779 c.2773C>A p.P925T Substitution - Missense 22:41150154-41150154 + PD11166a COSM5945453 c.1336G>T p.G446C Substitution - Missense 22:41131441-41131441 + ESCC_BICR_038T COSM1661670 c.4519G>A p.D1507N Substitution - Missense 22:41172565-41172565 + CSCC-41-T COSM4448719 c.1203delA p.H402fs*29 Deletion - Frameshift 22:41129924-41129924 + LUAD-RT-S01831 COSM384420 c.1335_1336GG>TT p.G446C Substitution - Missense 22:41131440-41131441 + TCGA-AK-3428-01 COSM3363712 c.1836T>C p.A612A Substitution - coding silent 22:41140215-41140215 + ESCC_BICR_053T COSM5442150 c.4867C>T p.L1623L Substitution - coding silent 22:41176334-41176334 + TCGA-HC-7817-01 COSM1416492 c.5485C>T p.R1829C Substitution - Missense 22:41177196-41177196 + S02385 COSM5698871 c.5462G>T p.R1821L Substitution - Missense 22:41177173-41177173 + ATL279 COSM5707674 c.1933G>T p.E645* Substitution - Nonsense 22:41141102-41141102 + HCT116 COSM96433 c.5095delA p.N1700fs*9 Deletion - Frameshift 22:41176806-41176806 + DM55 COSM5608368 c.2351C>T p.P784L Substitution - Missense 22:41149147-41149147 + S00089 COSM4387046 c.2534C>G p.T845S Substitution - Missense 22:41149915-41149915 + PD6194a COSM4385260 c.4585C>T p.R1529* Substitution - Nonsense 22:41172631-41172631 + UM-SCC-4 COSM3153139 c.3602G>A p.C1201Y Substitution - Missense 22:41160653-41160653 + TCGA-BT-A20X-01 COSM1308214 c.6754G>T p.E2252* Substitution - Nonsense 22:41178465-41178465 + 2334188 COSM97816 c.4154G>T p.C1385F Substitution - Missense 22:41168849-41168849 + TCGA-MY-A5BE-01 COSM122851 c.4195G>A p.D1399N Substitution - Missense 22:41169525-41169525 + 9T COSM109661 c.4933C>A p.R1645R Substitution - coding silent 22:41176400-41176400 + 5_tFL COSM221269 c.1244T>C p.L415P Substitution - Missense 22:41129965-41129965 + PD6133a COSM4104430 c.1442C>T p.P481L Substitution - Missense 22:41131547-41131547 + PD5773a COSM4385242 c.1898T>C p.L633P Substitution - Missense 22:41141067-41141067 + TCGA-DB-A64V-01 COSM3972987 c.4353T>C p.H1451H Substitution - coding silent 22:41170472-41170472 + OVACAR8 COSM96513 c.5188delT p.S1730fs*4 Deletion - Frameshift 22:41176899-41176899 + B96 COSM255054 c.644_654del11 p.G216fs*2 Deletion - Frameshift 22:41117736-41117746 + PT08_1 COSM5894123 c.724C>T p.L242F Substitution - Missense 22:41117816-41117816 + TCGA-AZ-6601-01 COSM1416490 c.5193C>T p.R1731R Substitution - coding silent 22:41176904-41176904 + CSCC-62-T COSM13867 c.4355C>T p.P1452L Substitution - Missense 22:41170474-41170474 + CN-AML-13-T COSM5424838 c.3501+2T>A p.? Unknown 22:41157410-41157410 + 5_tFL COSM220521 c.4399T>A p.Y1467N Substitution - Missense 22:41170518-41170518 + BD124T COSM5494219 c.123C>T p.H41H Substitution - coding silent 22:41117215-41117215 + HN_00361 COSM127888 c.924G>A p.P308P Substitution - coding silent 22:41127504-41127504 + ESCC-F42 COSM5047783 c.2377C>G p.Q793E Substitution - Missense 22:41149173-41149173 + Pat_02_B COSM5859458 c.4003G>A p.V1335I Substitution - Missense 22:41168577-41168577 + TCGA-D1-A16X-01 COSM1034554 c.3853G>T p.E1285* Substitution - Nonsense 22:41166645-41166645 + CSCC-27-T COSM3153144 c.3695C>T p.S1232F Substitution - Missense 22:41162746-41162746 + 3N64-VS-3T64 COSM727028 c.4241A>G p.Y1414C Substitution - Missense 22:41169571-41169571 + ML_77_T_01 COSM445042 c.5553T>C p.T1851T Substitution - coding silent 22:41177264-41177264 + 3N60-VS-3T60 COSM4984325 c.3699G>A p.K1233K Substitution - coding silent 22:41162750-41162750 + TCGA-AA-3527-01 COSM291806 c.1810C>G p.R604G Substitution - Missense 22:41140189-41140189 + TCGA-B5-A0JY-01 COSM274975 c.1739G>A p.R580Q Substitution - Missense 22:41137769-41137769 + SJTALL007 COSM306019 c.1879-1G>A p.? Unknown 22:41141047-41141047 + 99 COSM4169967 c.1913A>G p.Y638C Substitution - Missense 22:41141082-41141082 + TCGA-FV-A23B-01 COSM4914243 c.2469T>C p.P823P Substitution - coding silent 22:41149850-41149850 + T578 COSM4681095 c.6166C>T p.R2056W Substitution - Missense 22:41177877-41177877 + BD245T COSM5520012 c.3591-7C>T p.? Unknown 22:41160635-41160635 + STC263 COSM3681448 c.5412G>A p.P1804P Substitution - coding silent 22:41177123-41177123 + TCGA-D8-A1XK-01 COSM3842762 c.4608A>T p.E1536D Substitution - Missense 22:41172654-41172654 + ESCC_55 COSM5631924 c.1765C>A p.Q589K Substitution - Missense 22:41140144-41140144 + Patu8988t COSM96428 c.3143_3590del448 p.I1048fs*30 Deletion - Frameshift tumor_4160468 COSM3357344 c.4399T>G p.Y1467D Substitution - Missense 22:41170518-41170518 + V85 COSM727028 c.4241A>G p.Y1414C Substitution - Missense 22:41169571-41169571 + TCGA-EE-A3JD-06 COSM4396197 c.656T>C p.L219P Substitution - Missense 22:41117748-41117748 + PD7847a COSM305992 c.4916T>C p.L1639P Substitution - Missense 22:41176383-41176383 + TCGA-EP-A26S-01 COSM4913673 c.3764A>T p.H1255L Substitution - Missense 22:41164088-41164088 + KYSE-510 COSM3153135 c.3241C>T p.P1081S Substitution - Missense 22:41155093-41155093 + 587278 COSM1205372 c.5807C>T p.A1936V Substitution - Missense 22:41177518-41177518 + TCGA-BR-4201-01 COSM4104429 c.1109G>A p.R370H Substitution - Missense 22:41127689-41127689 + RK261_C01 COSM4778381 c.3074A>G p.E1025G Substitution - Missense 22:41152282-41152282 + TCGA-A8-A0A6-01 COSM3842761 c.4161A>C p.P1387P Substitution - coding silent 22:41168856-41168856 + TCGA-BR-A4QL-01 COSM88784 c.4879C>T p.R1627W Substitution - Missense 22:41176346-41176346 + 585210 COSM320129 c.5189C>T p.S1730F Substitution - Missense 22:41176900-41176900 + ESCC_162 COSM122851 c.4195G>A p.D1399N Substitution - Missense 22:41169525-41169525 + B24 COSM122851 c.4195G>A p.D1399N Substitution - Missense 22:41169525-41169525 + TCGA-FS-A1ZK-06 COSM3554893 c.5630C>T p.P1877L Substitution - Missense 22:41177341-41177341 + 587256 COSM1205374 c.5585A>C p.Q1862P Substitution - Missense 22:41177296-41177296 + BICR_22 COSM1716512 c.4540G>A p.E1514K Substitution - Missense 22:41172586-41172586 + SJTALL168 COSM4603609 c.4894_4895insGGACCA p.L1631_T1632insRT Insertion - In frame 22:41176361-41176362 + 7098 COSM5751396 c.5784G>CG p.M1928fs*145 Complex - frameshift 22:41177495-41177495 + ESCC_115 COSM727028 c.4241A>G p.Y1414C Substitution - Missense 22:41169571-41169571 + ESCC-F68 COSM96419 c.4195G>T p.D1399Y Substitution - Missense 22:41169525-41169525 + 464 COSM88793 c.4617+1G>A p.? Unknown 22:41172664-41172664 + ESCC-F15 COSM122851 c.4195G>A p.D1399N Substitution - Missense 22:41169525-41169525 + KM12 COSM13867 c.4355C>T p.P1452L Substitution - Missense 22:41170474-41170474 + ESO-184 COSM1251230 c.4607A>G p.E1536G Substitution - Missense 22:41172653-41172653 + PTC-50C COSM4156325 c.5335T>G p.C1779G Substitution - Missense 22:41177046-41177046 + PD6879a COSM4385244 c.2359G>A p.G787S Substitution - Missense 22:41149155-41149155 + CSCC-27-T COSM4466563 c.1441C>T p.P481S Substitution - Missense 22:41131546-41131546 + 2321295 COSM4774848 c.5359G>T p.A1787S Substitution - Missense 22:41177070-41177070 + TCGA-CG-5721-01 COSM4104438 c.5459A>G p.H1820R Substitution - Missense 22:41177170-41177170 + 2432697 COSM5352316 c.? p.R1599H Substitution - Missense HT115 COSM1034568 c.4512C>T p.F1504F Substitution - coding silent 22:41172558-41172558 + PD8361a COSM5944414 c.6567_6571delGCAAC p.M2189fs*19 Deletion - Frameshift 22:41178278-41178282 + PD9316a COSM3153139 c.3602G>A p.C1201Y Substitution - Missense 22:41160653-41160653 + CSCC-41-T COSM3153237 c.7073C>T p.P2358L Substitution - Missense 22:41178784-41178784 + 2364042 COSM4169705 c.? p.P925T Substitution - Missense 260211 COSM3726179 c.3482G>C p.G1161A Substitution - Missense 22:41157389-41157389 + NB-1744 COSM1284744 c.2743C>T p.R915C Substitution - Missense 22:41150124-41150124 + 460 COSM1716512 c.4540G>A p.E1514K Substitution - Missense 22:41172586-41172586 + PD5724a COSM4385265 c.6796_6798delCAG p.Q2268delQ Deletion - In frame 22:41178507-41178509 + PT50 COSM5937892 c.2536C>T p.P846S Substitution - Missense 22:41149917-41149917 + OSCC-GB_00380111 COSM3153139 c.3602G>A p.C1201Y Substitution - Missense 22:41160653-41160653 + Pat_76_A COSM84765 c.3671+1G>A p.? Unknown 22:41160723-41160723 + CHC303T COSM4957844 c.6223C>A p.H2075N Substitution - Missense 22:41177934-41177934 + TCGA-CD-A4MH-01 COSM4104439 c.6048G>A p.M2016I Substitution - Missense 22:41177759-41177759 + MATU COSM96431 c.5061+2T>A p.? Unknown 22:41176530-41176530 + cSCCP4 COSM139231 c.6907C>T p.L2303F Substitution - Missense 22:41178618-41178618 + DLBCL-PatientG COSM220522 c.4399T>C p.Y1467H Substitution - Missense 22:41170518-41170518 + 8066503 COSM3785677 c.5568G>A p.T1856T Substitution - coding silent 22:41177279-41177279 + TCGA-EW-A423-01 COSM3842760 c.1440G>A p.M480I Substitution - Missense 22:41131545-41131545 + TCGA-FW-A3R5-06 COSM3912893 c.4060C>T p.P1354S Substitution - Missense 22:41168755-41168755 + TCGA-FD-A3B8-01 COSM1308204 c.2482C>T p.H828Y Substitution - Missense 22:41149863-41149863 + TL84 COSM5752091 c.4879_4880insT p.R1627fs*46 Insertion - Frameshift 22:41176346-41176347 + TCGA-BS-A0UF-01 COSM1034560 c.4051G>T p.E1351* Substitution - Nonsense 22:41168746-41168746 + MN-298 COSM1578560 c.2777delC p.P927fs*19 Deletion - Frameshift 22:41150158-41150158 + T3535 COSM4104429 c.1109G>A p.R370H Substitution - Missense 22:41127689-41127689 + B80-8 COSM254671 c.193C>T p.Q65* Substitution - Nonsense 22:41117285-41117285 + TCGA-BS-A0UF-01 COSM1034515 c.936G>T p.Q312H Substitution - Missense 22:41127516-41127516 + DM14 COSM3153105 c.1777C>T p.P593S Substitution - Missense 22:41140156-41140156 + 388 COSM122851 c.4195G>A p.D1399N Substitution - Missense 22:41169525-41169525 + I2L-P19Tb-Tumor-Organoid COSM5366485 c.4351C>A p.H1451N Substitution - Missense 22:41170470-41170470 + 1N43-VS-1T43 COSM318349 c.4508A>C p.Y1503S Substitution - Missense 22:41172554-41172554 + TCGA-B5-A11E-01 COSM187721 c.4886C>T p.A1629V Substitution - Missense 22:41176353-41176353 + CSCC-35-T COSM4501287 c.584C>T p.S195L Substitution - Missense 22:41117676-41117676 + BD40T COSM5509226 c.3345G>T p.W1115C Substitution - Missense 22:41157252-41157252 + 5_FL COSM221269 c.1244T>C p.L415P Substitution - Missense 22:41129965-41129965 + CoCa19 COSM96432 c.? p.? Unknown 1964120 COSM88790 c.4408delA p.M1470fs*26 Deletion - Frameshift 22:41170527-41170527 + ATL021 COSM5707675 c.1951A>T p.R651* Substitution - Nonsense 22:41141120-41141120 + TCGA-FU-A3NI-01 COSM4849197 c.5155C>T p.Q1719* Substitution - Nonsense 22:41176866-41176866 + 1685503 COSM235738 c.3442_3447delGTCTTT p.V1148_F1149delVF Deletion - In frame 22:41157349-41157354 + PD9342a COSM5945459 c.3682A>T p.K1228* Substitution - Nonsense 22:41162733-41162733 + HCT-116 COSM1684652 c.5099delA p.N1700fs*9 Deletion - Frameshift 22:41176810-41176810 + KM12 COSM13867 c.4355C>T p.P1452L Substitution - Missense 22:41170474-41170474 + SUDHL2 COSM88789 c.2461C>T p.Q821* Substitution - Nonsense 22:41149842-41149842 + 587228 COSM1205369 c.4397G>T p.W1466L Substitution - Missense 22:41170516-41170516 + TCGA-EK-A2RK-01 COSM4828896 c.2437C>T p.Q813* Substitution - Nonsense 22:41149818-41149818 + I2L-P19Tb-Tumor-Biopsy COSM5366488 c.454G>T p.G152C Substitution - Missense 22:41117546-41117546 + PD8934a COSM4385269 c.7126C>A p.L2376I Substitution - Missense 22:41178837-41178837 + P13 COSM5009621 c.2989A>G p.I997V Substitution - Missense 22:41152004-41152004 + ATL376 COSM5707672 c.1542G>T p.M514I Substitution - Missense 22:41135826-41135826 + 2228019 COSM4171998 c.? p.C369F Substitution - Missense 587332 COSM1205373 c.3548G>A p.C1183Y Substitution - Missense 22:41158458-41158458 + Pat_45_B COSM5859459 c.4529C>A p.P1510H Substitution - Missense 22:41172575-41172575 + TCGA-BT-A3PH-01 COSM1308201 c.40A>C p.K14Q Substitution - Missense 22:41093044-41093044 + PT13 COSM5896458 c.3781C>T p.H1261Y Substitution - Missense 22:41164105-41164105 + TCGA-A2-A0T5-01 COSM3842764 c.5528A>C p.Q1843P Substitution - Missense 22:41177239-41177239 + CSCC-7-T COSM4450101 c.4453-1G>A p.? Unknown 22:41172498-41172498 + 2227999 COSM4171996 c.? p.? Unknown PD6898a COSM4385258 c.4183_4184delAT p.S1396fs*4 Deletion - Frameshift 22:41169513-41169514 + TCGA-BR-4256-01 COSM4104431 c.1528+2T>C p.? Unknown 22:41131635-41131635 + TCGA-BS-A0TA-01 COSM1034562 c.4189T>G p.Y1397D Substitution - Missense 22:41169519-41169519 + TCGA-CA-6717-01 COSM1416491 c.5331C>T p.G1777G Substitution - coding silent 22:41177042-41177042 + HCC2998 COSM1682284 c.1393G>T p.E465* Substitution - Nonsense 22:41131498-41131498 + Pat_15_B COSM5859463 c.6664_6666delCAG p.Q2225delQ Deletion - In frame 22:41178375-41178377 + Pat_44_A COSM5859455 c.3226C>T p.R1076C Substitution - Missense 22:41155078-41155078 + A7 COSM5350690 c.7065G>T p.Q2355H Substitution - Missense 22:41178776-41178776 + 2334195 COSM320131 c.4364A>G p.Q1455R Substitution - Missense 22:41170483-41170483 + B96 COSM255054 c.644_654del11 p.G216fs*2 Deletion - Frameshift 22:41117736-41117746 + B106 COSM254667 c.4454A>T p.D1485V Substitution - Missense 22:41172500-41172500 + PD6494a COSM4170086 c.6626_6637del12 p.N2209_Q2213>K Complex - deletion inframe 22:41178337-41178348 + RK057_C01 COSM3701763 c.3281A>G p.K1094R Substitution - Missense 22:41157188-41157188 + TCGA-DK-A1A7-01 COSM419539 c.3284G>T p.S1095I Substitution - Missense 22:41157191-41157191 + TCGA-CU-A0YR-01 COSM419540 c.49A>G p.K17E Substitution - Missense 22:41093053-41093053 + KYSE510 COSM3153135 c.3241C>T p.P1081S Substitution - Missense 22:41155093-41155093 + ESCC_3 COSM727028 c.4241A>G p.Y1414C Substitution - Missense 22:41169571-41169571 + 18T COSM3713703 c.6856C>A p.P2286T Substitution - Missense 22:41178567-41178567 + CHC1704T COSM4804090 c.1401C>G p.A467A Substitution - coding silent 22:41131506-41131506 + 7441 COSM1644572 c.4286+1G>T p.? Unknown 22:41169617-41169617 + RK126_C01 COSM1632621 c.3391T>A p.Y1131N Substitution - Missense 22:41157298-41157298 + CHC2141T COSM4790209 c.5638C>A p.P1880T Substitution - Missense 22:41177349-41177349 + P7 COSM5009814 c.3087G>A p.Q1029Q Substitution - coding silent 22:41152295-41152295 + TCGA-BS-A0UF-01 COSM1034556 c.3977T>C p.V1326A Substitution - Missense 22:41168551-41168551 + PD8028a COSM5945454 c.2241+5G>A p.? Unknown 22:41147951-41147951 + 34T COSM3713737 c.511G>T p.A171S Substitution - Missense 22:41117603-41117603 + PD8141a COSM5945462 c.5043G>A p.W1681* Substitution - Nonsense 22:41176510-41176510 + PD7371a COSM4385247 c.2645C>G p.P882R Substitution - Missense 22:41150026-41150026 + CSCC-32-T COSM4455339 c.736A>T p.M246L Substitution - Missense 22:41125870-41125870 + TCGA-D9-A6EC-06 COSM4404560 c.3360T>C p.D1120D Substitution - coding silent 22:41157267-41157267 + CN-AML-NR-32-Dx COSM5424838 c.3501+2T>A p.? Unknown 22:41157410-41157410 + TCGA-B0-5713-01 COSM478996 c.498C>A p.N166K Substitution - Missense 22:41117590-41117590 + 1964031 COSM1651571 c.6970_6971insC p.H2324fs*55 Insertion - Frameshift 22:41178681-41178682 + TCGA-AX-A0J0-01 COSM1034509 c.95-2A>G p.? Unknown 22:41117185-41117185 + 53 COSM4170086 c.6626_6637del12 p.N2209_Q2213>K Complex - deletion inframe 22:41178337-41178348 + B86-Tumor COSM88784 c.4879C>T p.R1627W Substitution - Missense 22:41176346-41176346 + YES2 COSM97816 c.4154G>T p.C1385F Substitution - Missense 22:41168849-41168849 + TCGA-56-1622-01 COSM727029 c.4193T>C p.L1398P Substitution - Missense 22:41169523-41169523 + CEM COSM96517 c.3262-2A>G p.? Unknown 22:41157167-41157167 + TCGA-C8-A27B-01 COSM1484264 c.4352A>C p.H1451P Substitution - Missense 22:41170471-41170471 + TCGA-AA-3713-01 COSM1416465 c.444G>A p.T148T Substitution - coding silent 22:41117536-41117536 + PD7623a COSM5945456 c.3425G>T p.C1142F Substitution - Missense 22:41157332-41157332 + V57 COSM727028 c.4241A>G p.Y1414C Substitution - Missense 22:41169571-41169571 + BD232T COSM5501573 c.2858A>G p.N953S Substitution - Missense 22:41151873-41151873 + DM55 COSM5608367 c.4712C>T p.P1571L Substitution - Missense 22:41173717-41173717 + TCGA-AA-3715-01 COSM269098 c.2512C>T p.R838C Substitution - Missense 22:41149893-41149893 + PD8470a COSM5945464 c.6889C>T p.Q2297* Substitution - Nonsense 22:41178600-41178600 + PD6816a COSM4385238 c.899C>T p.P300L Substitution - Missense 22:41126033-41126033 + TCGA-B5-A0JY-01 COSM1034571 c.4933C>T p.R1645* Substitution - Nonsense 22:41176400-41176400 + TCGA-BS-A0UF-01 COSM1034568 c.4512C>T p.F1504F Substitution - coding silent 22:41172558-41172558 + TCGA-AP-A0LM-01 COSM1034517 c.1436A>C p.Q479P Substitution - Missense 22:41131541-41131541 + FARAGE COSM88790 c.4408delA p.M1470fs*26 Deletion - Frameshift 22:41170527-41170527 + S04-6933-TP COSM4991536 c.6897C>T p.I2299I Substitution - coding silent 22:41178608-41178608 + TCGA-B0-4811-01 COSM478999 c.6022T>C p.S2008P Substitution - Missense 22:41177733-41177733 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.517505;Hs.517517 22q13.2 602700

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C IntronicSNV . c.907-97A>C 22 41523394 CLL A C Missense p.H1451P c.4352A>C 22 41566475 BRCA A C Missense p.K14Q c.40A>C 22 41489048 BLCA A C Missense p.N2379H c.7135A>C 22 41574850 HNSC A - Frameshift p.I61Lfs*55 c.181delA 22 41513277 UCEC A G Missense p.E1536G c.4607A>G 22 41568657 ESCA A G Missense p.E2360G c.7079A>G 22 41574794 RCCC A G Missense p.H1377R c.4130A>G 22 41564829 COREAD A G Missense p.H1451R c.4352A>G 22 41566475 UCEC A G Missense p.I807V c.2419A>G 22 41545804 HNSC A G Missense p.K1760R c.5279A>G 22 41572994 RCCC A G Missense p.K17E c.49A>G 22 41489057 BLCA A G Missense p.M749V c.2245A>G 22 41545045 BLCA A G Missense p.N1126S c.3377A>G 22 41553288 UCEC A G Missense p.N1286S c.3857A>G 22 41562653 SCLC A G Missense p.N656S c.1967A>G 22 41537140 CM A G Missense p.Q1455R c.4364A>G 22 41566487 SCLC A G Missense p.Y1414C c.4241A>G 22 41565575 LUSC A G Missense p.Y1446C c.4337A>G 22 41566460 HNSC A G Missense p.Y207C c.620A>G 22 41513716 STAD A G SpliceAcceptorSNV . c.1529-2A>G 22 41531815 UCEC A G SpliceAcceptorSNV . c.4173-2A>G 22 41565505 LUSC A G Synonymous p.G1347G c.4041A>G 22 41564740 GBM A G Synonymous p.P708P c.2124A>G 22 41542813 UCEC A T Missense p.D1485V c.4454A>T 22 41568504 CLL A T Missense p.H1451L c.4352A>T 22 41566475 CLL A T Missense p.K1459M c.4376A>T 22 41566499 RCCC A T Nonsense p.K1407* c.4219A>T 22 41565553 MM C A Missense p.F2211L c.6633C>A 22 41574348 MB C A Missense p.H2125Q c.6375C>A 22 41574090 LUSC C A Missense p.N166K c.498C>A 22 41513594 RCCC C A Missense p.Q2215K c.6643C>A 22 41574358 RCCC C A Missense p.Q2281K c.6841C>A 22 41574556 STAD C A Missense p.T1878N c.5633C>A 22 41573348 LUSC C A Nonsense p.C1771* c.5313C>A 22 41573028 HNSC C A Nonsense p.S24* c.71C>A 22 41489079 HNSC CC GT Missense p.P157V c.469_470delinsGT 22 41513565 CM CC TT 5-UTRBlockSubstitution . c.1-432_1-431delinsTT 22 41488577 CM CC TT Missense p.P1620L c.4859_4860delinsTT 22 41572330 CM C - Frameshift p.Q1648Sfs*61 c.4942delC 22 41572411 BLCA C G IntronicSNV . c.4453-3C>G 22 41568500 SCLC C G Missense p.D618E c.1854C>G 22 41536237 BRCA C G Missense p.H631D c.1891C>G 22 41537064 BLCA C G Missense p.I1739M c.5217C>G 22 41572932 BLCA C G Missense p.N1389K c.4167C>G 22 41564866 HNSC C G Missense p.Q2002E c.6004C>G 22 41573719 BLCA C G Missense p.R604G c.1810C>G 22 41536193 COREAD C G Synonymous p.L1788L c.5364C>G 22 41573079 BLCA C G Synonymous p.L2041L c.6123C>G 22 41573838 BLCA C G Synonymous p.L2058L c.6174C>G 22 41573889 BLCA C G Synonymous p.L2058L c.6174C>G 22 41573889 CM C T Missense p.A1629V c.4886C>T 22 41572357 UCEC C T Missense p.A327V c.980C>T 22 41523564 BRCA C T Missense p.H828Y c.2482C>T 22 41545867 BLCA C T Missense p.L1828F c.5482C>T 22 41573197 CM C T Missense p.P1863S c.5587C>T 22 41573302 ESCA C T Missense p.P1877L c.5630C>T 22 41573345 CM C T Missense p.P500L c.1499C>T 22 41527608 CM C T Missense p.P886L c.2657C>T 22 41546042 CM C T Missense p.R1627W c.4879C>T 22 41572350 CLL C T Missense p.R1627W c.4879C>T 22 41572350 CM C T Missense p.R1737C c.5209C>T 22 41572924 STAD C T Missense p.R1829C c.5485C>T 22 41573200 PRAD C T Missense p.R2088W c.6262C>T 22 41573977 PRAD C T Missense p.S1642F c.4925C>T 22 41572396 CM C T Missense p.S1730F c.5189C>T 22 41572904 SCLC C T Missense p.S833L c.2498C>T 22 41545883 BRCA C T Missense p.T66I c.197C>T 22 41513293 COREAD C T Nonsense p.Q2048* c.6142C>T 22 41573857 LUAD C T Nonsense p.Q2297* c.6889C>T 22 41574604 CM C T Nonsense p.Q2298* c.6892C>T 22 41574607 UCEC C T Nonsense p.Q523* c.1567C>T 22 41531855 HNSC C T Nonsense p.Q65* c.193C>T 22 41513289 BLCA C T Nonsense p.Q767* c.2299C>T 22 41545099 BRCA C T Nonsense p.Q829* c.2485C>T 22 41545870 BLCA C T Nonsense p.Q874* c.2620C>T 22 41546005 CLL C T Nonsense p.Q898* c.2692C>T 22 41546077 NB C T Nonsense p.Q965* c.2893C>T 22 41547912 HNSC C T Nonsense p.R1281* c.3841C>T 22 41562637 UCEC C T Nonsense p.R1312* c.3934C>T 22 41564512 OV C T Nonsense p.R1645* c.4933C>T 22 41572404 BLCA C T Synonymous p.A861A c.2583C>T 22 41545968 CM C T Synonymous p.D1664D c.4992C>T 22 41572463 CM C T Synonymous p.G750G c.2250C>T 22 41545050 STAD C T Synonymous p.L1371L c.4111C>T 22 41564810 GBM C T Synonymous p.L633L c.1897C>T 22 41537070 CM C T Synonymous p.Y1066Y c.3198C>T 22 41551054 CM G A Missense p.A903T c.2707G>A 22 41546092 HNSC G A Missense p.C1164Y c.3491G>A 22 41553402 BLCA G A Missense p.C1164Y c.3491G>A 22 41553402 HNSC G A Missense p.C1201Y c.3602G>A 22 41556657 GBM G A Missense p.C1204Y c.3611G>A 22 41556666 HNSC G A Missense p.C1385Y c.4154G>A 22 41564853 BLCA G A Missense p.C382Y c.1145G>A 22 41523729 COREAD G A Missense p.D1273N c.3817G>A 22 41562613 BLCA G A Missense p.D1399N c.4195G>A 22 41565529 HNSC G A Missense p.D1399N c.4195G>A 22 41565529 LUSC G A Missense p.E1514K c.4540G>A 22 41568590 HNSC G A Missense p.E360K c.1078G>A 22 41523662 CM G A Missense p.E546K c.1636G>A 22 41533670 ESCA G A Missense p.E948K c.2842G>A 22 41547861 HNSC G A Missense p.G1983R c.5947G>A 22 41573662 CM G A Missense p.G497E c.1490G>A 22 41527599 CM G A Missense p.R1187H c.3560G>A 22 41554474 UCEC G A Missense p.R1356Q c.4067G>A 22 41564766 STAD G A Missense p.R370H c.1109G>A 22 41523693 STAD G A Missense p.R580Q c.1739G>A 22 41533773 STAD G A Missense p.S697N c.2090G>A 22 41542779 BRCA G A SpliceAcceptorSNV . c.4780-1G>A 22 41572250 HNSC G A SpliceDonorSNV . c.3671+1G>A 22 41556727 PAAD G A Synonymous p.A627A c.1881G>A 22 41537054 HNSC G A Synonymous p.E1678E c.5034G>A 22 41572505 LUAD G A Synonymous p.P308P c.924G>A 22 41523508 HNSC G A Synonymous p.Q2268Q c.6804G>A 22 41574519 HNSC G A Synonymous p.V6V c.18G>A 22 41489026 BRCA G C Missense p.E1526D c.4578G>C 22 41568628 BLCA G C Missense p.G1375R c.4123G>C 22 41564822 SCLC G C Missense p.L1409F c.4227G>C 22 41565561 BLCA G C Missense p.Q1455H c.4365G>C 22 41566488 BLCA G C Missense p.W1466C c.4398G>C 22 41566521 HNSC G C Synonymous p.G137G c.411G>C 22 41513507 CM - G Frameshift p.A1490Gfs*3 c.4468dupG 22 41568518 UCEC - G Frameshift p.F1270Ifs*4 c.3806+1dupG 22 41560133 BLCA - G Frameshift p.G502Rfs*11 c.1502_1503insG 22 41527611 BRCA G T Missense p.A1602S c.4804G>T 22 41572275 HNSC G T Missense p.C1385F c.4154G>T 22 41564853 HNSC G T Missense p.C1385F c.4154G>T 22 41564853 SCLC G T Missense p.D1367Y c.4099G>T 22 41564798 CM G T Missense p.D1399Y c.4195G>T 22 41565529 BLCA G T Missense p.D1485Y c.4453G>T 22 41568503 LUAD G T Missense p.G142V c.425G>T 22 41513521 HNSC G T Missense p.G2123W c.6367G>T 22 41574082 LUSC G T Missense p.R1830S c.5490G>T 22 41573205 PRAD G T Missense p.R648L c.1943G>T 22 41537116 CM G T Missense p.S1095I c.3284G>T 22 41553195 BLCA G T Nonsense p.E1640* c.4918G>T 22 41572389 CM G T Nonsense p.E1672* c.5014G>T 22 41572485 UCEC G T Nonsense p.E2252* c.6754G>T 22 41574469 BLCA G T Nonsense p.G515* c.1543G>T 22 41531831 UCEC T A Missense p.Y1131N c.3391T>A 22 41553302 HC TCC - InFrameDeletion p.P1453delP c.4357_4359delCCT 22 41566476 HNSC T C Missense p.C1372R c.4114T>C 22 41564813 SCLC T C Missense p.C1438R c.4312T>C 22 41566435 DLBCL T C Missense p.I947T c.2840T>C 22 41547859 CLL T C Missense p.L1398P c.4193T>C 22 41565527 LUSC T C Missense p.L219P c.656T>C 22 41513752 CM T C Missense p.S1849P c.5545T>C 22 41573260 HNSC T C Missense p.S2008P c.6022T>C 22 41573737 RCCC T C SpliceDonorSNV . c.1528+2T>C 22 41527639 STAD T C Synonymous p.A612A c.1836T>C 22 41536219 RCCC - T Frameshift p.K1488Ifs*5 c.4462_4463insT 22 41568512 PAAD T G Missense p.F1343C c.4028T>G 22 41564727 HNSC T G Missense p.Y1397D c.4189T>G 22 41565523 UCEC T G Missense p.Y257D c.769T>G 22 41521907 LUSC T G Synonymous p.V2273V c.6819T>G 22 41574534 COREAD T - IntronicDeletion . c.2818-9delT 22 41547821 STAD