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 16 68867311 68867314 + Frame_Shift_Del DEL CAGA CAGA - TCGA-P6-A5OH-01A-11D-A30A-10 TCGA-P6-A5OH-11A-01D-A30A-10 g.chr16:68867311_68867314delCAGA c.2558_2561delCAGA c.(2557-2562)tcagacfs p.SD853fs BLCA 16 68835596 68835596 + Nonsense_Mutation SNP C C T TCGA-XF-AAN0-01A-11D-A42E-08 TCGA-XF-AAN0-10A-01D-A42H-08 g.chr16:68835596C>T c.187C>T c.(187-189)Cga>Tga p.R63* BLCA 16 68835597 68835597 + Missense_Mutation SNP G G C TCGA-XF-A9T3-01A-11D-A42E-08 TCGA-XF-A9T3-10A-01D-A42H-08 g.chr16:68835597G>C c.188G>C c.(187-189)cGa>cCa p.R63P BLCA 16 68835746 68835746 + Missense_Mutation SNP A A G TCGA-H4-A2HQ-01A-11D-A17V-08 TCGA-H4-A2HQ-10A-01D-A17V-08 g.chr16:68835746A>G c.337A>G c.(337-339)Aaa>Gaa p.K113E BLCA 16 68842337 68842337 + Missense_Mutation SNP C C T TCGA-C4-A0F0-01A-12D-A10S-08 TCGA-C4-A0F0-10A-01D-A10S-08 g.chr16:68842337C>T c.398C>T c.(397-399)tCt>tTt p.S133F BLCA 16 68842438 68842438 + Nonsense_Mutation SNP G G T TCGA-KQ-A41S-01A-12D-A339-08 TCGA-KQ-A41S-10C-01D-A339-08 g.chr16:68842438G>T c.499G>T c.(499-501)Gaa>Taa p.E167* BLCA 16 68842716 68842716 + Nonsense_Mutation SNP G G T TCGA-KQ-A41S-01A-12D-A339-08 TCGA-KQ-A41S-10C-01D-A339-08 g.chr16:68842716G>T c.652G>T c.(652-654)Gag>Tag p.E218* BLCA 16 68844139 68844139 + Missense_Mutation SNP G G C TCGA-G2-A3IE-01A-11D-A20D-08 TCGA-G2-A3IE-10A-01D-A20D-08 g.chr16:68844139G>C c.727G>C c.(727-729)Gag>Cag p.E243Q BLCA 16 68844153 68844153 + Silent SNP G G A TCGA-G2-A2EL-01A-12D-A18F-08 TCGA-G2-A2EL-10A-01D-A18F-08 g.chr16:68844153G>A c.741G>A c.(739-741)gaG>gaA p.E247E BLCA 16 68845691 68845691 + Missense_Mutation SNP G G A TCGA-G2-A3IE-01A-11D-A20D-08 TCGA-G2-A3IE-10A-01D-A20D-08 g.chr16:68845691G>A c.937G>A c.(937-939)Gac>Aac p.D313N BLCA 16 68846080 68846080 + Nonsense_Mutation SNP C C T TCGA-G2-AA3D-01A-11D-A391-08 TCGA-G2-AA3D-10A-01D-A394-08 g.chr16:68846080C>T c.1051C>T c.(1051-1053)Caa>Taa p.Q351* BLCA 16 68846154 68846154 + Silent SNP C C T TCGA-2F-A9KR-01A-11D-A38G-08 TCGA-2F-A9KR-10A-01D-A38J-08 g.chr16:68846154C>T c.1125C>T c.(1123-1125)ttC>ttT p.F375F BLCA 16 68847234 68847234 + Missense_Mutation SNP G G A TCGA-DK-A1AG-01A-11D-A13W-08 TCGA-DK-A1AG-10A-01D-A13W-08 g.chr16:68847234G>A c.1156G>A c.(1156-1158)Gag>Aag p.E386K BLCA 16 68847275 68847277 + In_Frame_Del DEL TGA TGA - TCGA-HQ-A2OF-01A-11D-A26M-08 TCGA-HQ-A2OF-10B-01D-A26K-08 g.chr16:68847275_68847277delTGA c.1197_1199delTGA c.(1195-1200)actgat>act p.D400del BLCA 16 68849604 68849604 + Nonsense_Mutation SNP C C T TCGA-XF-A9SX-01A-21D-A391-08 TCGA-XF-A9SX-10A-01D-A394-08 g.chr16:68849604C>T c.1507C>T c.(1507-1509)Cag>Tag p.Q503* BLCA 16 68855960 68855960 + Missense_Mutation SNP G G A TCGA-DK-AA6Q-01A-11D-A391-08 TCGA-DK-AA6Q-10A-01D-A394-08 g.chr16:68855960G>A c.1768G>A c.(1768-1770)Gac>Aac p.D590N BLCA 16 68856020 68856020 + Nonsense_Mutation SNP C C T TCGA-XF-A9SL-01A-11D-A391-08 TCGA-XF-A9SL-10A-01D-A394-08 g.chr16:68856020C>T c.1828C>T c.(1828-1830)Cag>Tag p.Q610* BLCA 16 68856094 68856094 + Silent SNP G G A TCGA-K4-A54R-01A-11D-A26M-08 TCGA-K4-A54R-10A-01D-A26K-08 g.chr16:68856094G>A c.1902G>A c.(1900-1902)gcG>gcA p.A634A BLCA 16 68857307 68857307 + Nonsense_Mutation SNP G G T TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr16:68857307G>T c.1942G>T c.(1942-1944)Gaa>Taa p.E648* BLCA 16 68863653 68863653 + Missense_Mutation SNP C C G TCGA-GC-A3I6-01A-11D-A20D-08 TCGA-GC-A3I6-10A-01D-A20D-08 g.chr16:68863653C>G c.2392C>G c.(2392-2394)Ctt>Gtt p.L798V BRCA 16 68772203 68772204 + Frame_Shift_Ins INS - - CA TCGA-A2-A0SY-01A-31D-A099-09 TCGA-A2-A0SY-10A-01D-A099-09 g.chr16:68772203_68772204insCA c.52_53insCA c.(52-54)tccfs p.S18fs BRCA 16 68772218 68772218 + Nonsense_Mutation SNP C C T TCGA-AC-A3BB-01A-21D-A19Y-09 TCGA-AC-A3BB-10A-01D-A19Y-09 g.chr16:68772218C>T c.67C>T c.(67-69)Cag>Tag p.Q23* BRCA 16 68772218 68772218 + Nonsense_Mutation SNP C C T TCGA-B6-A0RQ-01A-11D-A10Y-09 TCGA-B6-A0RQ-10A-01D-A110-09 g.chr16:68772218C>T c.67C>T c.(67-69)Cag>Tag p.Q23* BRCA 16 68772218 68772218 + Nonsense_Mutation SNP C C T TCGA-B6-A40C-01A-11D-A23C-09 TCGA-B6-A40C-10A-01D-A23C-09 g.chr16:68772218C>T c.67C>T c.(67-69)Cag>Tag p.Q23* BRCA 16 68772218 68772218 + Nonsense_Mutation SNP C C T TCGA-D8-A1XO-01A-11D-A14K-09 TCGA-D8-A1XO-10A-01D-A14K-09 g.chr16:68772218C>T c.67C>T c.(67-69)Cag>Tag p.Q23* BRCA 16 68772218 68772218 + Nonsense_Mutation SNP C C T TCGA-D8-A27V-01A-12D-A17D-09 TCGA-D8-A27V-10A-01D-A17D-09 g.chr16:68772218C>T c.67C>T c.(67-69)Cag>Tag p.Q23* BRCA 16 68772218 68772218 + Nonsense_Mutation SNP C C T TCGA-LL-A50Y-01A-11D-A25Q-09 TCGA-LL-A50Y-10A-01D-A25Q-09 g.chr16:68772218C>T c.67C>T c.(67-69)Cag>Tag p.Q23* BRCA 16 68772257 68772257 + Frame_Shift_Del DEL A A - TCGA-BH-A18P-01A-11D-A12B-09 TCGA-BH-A18P-11A-43D-A12B-09 g.chr16:68772257delA c.106delA c.(106-108)agcfs p.S36fs BRCA 16 68835596 68835596 + Nonsense_Mutation SNP C C T TCGA-A2-A0CR-01A-11D-A228-09 TCGA-A2-A0CR-10A-01D-A22A-09 g.chr16:68835596C>T c.187C>T c.(187-189)Cga>Tga p.R63* BRCA 16 68835596 68835596 + Nonsense_Mutation SNP C C T TCGA-A2-A0YK-01A-22D-A117-09 TCGA-A2-A0YK-10A-01D-A117-09 g.chr16:68835596C>T c.187C>T c.(187-189)Cga>Tga p.R63* BRCA 16 68835596 68835596 + Nonsense_Mutation SNP C C T TCGA-AN-A03Y-01A-21W-A019-09 TCGA-AN-A03Y-10A-01W-A021-09 g.chr16:68835596C>T c.187C>T c.(187-189)Cga>Tga p.R63* BRCA 16 68835596 68835596 + Nonsense_Mutation SNP C C T TCGA-BH-A209-01A-11D-A17G-09 TCGA-BH-A209-11A-42D-A17G-09 g.chr16:68835596C>T c.187C>T c.(187-189)Cga>Tga p.R63* BRCA 16 68835599 68835600 + Frame_Shift_Ins INS - - A TCGA-GM-A3XN-01A-12D-A22X-09 TCGA-GM-A3XN-10A-01D-A22X-09 g.chr16:68835599_68835600insA c.190_191insA c.(190-192)caafs p.Q64fs BRCA 16 68835629 68835629 + Nonsense_Mutation SNP C C T TCGA-AR-A5QM-01A-11D-A27P-09 TCGA-AR-A5QM-10A-01D-A27P-09 g.chr16:68835629C>T c.220C>T c.(220-222)Cga>Tga p.R74* BRCA 16 68835665 68835666 + Frame_Shift_Del DEL AA AA - TCGA-AC-A2FF-01A-11D-A17D-09 TCGA-AC-A2FF-11A-13D-A17D-09 g.chr16:68835665_68835666delAA c.256_257delAA c.(256-258)aaafs p.K86fs BRCA 16 68835697 68835697 + Frame_Shift_Del DEL C C - TCGA-A7-A13H-01A-11D-A228-09 TCGA-A7-A13H-10A-01D-A22A-09 g.chr16:68835697delC c.288delC c.(286-288)atcfs p.I96fs BRCA 16 68842369 68842369 + Frame_Shift_Del DEL A A - TCGA-GM-A4E0-01A-12D-A25Q-09 TCGA-GM-A4E0-10A-01D-A25Q-09 g.chr16:68842369delA c.430delA c.(430-432)aacfs p.N144fs BRCA 16 68842414 68842414 + Frame_Shift_Del DEL C C - TCGA-BH-A0C1-01B-11D-A12B-09 TCGA-BH-A0C1-10A-01D-A12B-09 g.chr16:68842414delC c.475delC c.(475-477)cctfs p.P160fs BRCA 16 68842417 68842418 + Frame_Shift_Ins INS - - G TCGA-A2-A1FV-01A-11D-A13L-09 TCGA-A2-A1FV-10A-01D-A13O-09 g.chr16:68842417_68842418insG c.478_479insG c.(478-480)cccfs p.P160fs BRCA 16 68842432 68842432 + Missense_Mutation SNP G G C TCGA-AR-A2LJ-01A-12D-A19Y-09 TCGA-AR-A2LJ-10A-01D-A19Y-09 g.chr16:68842432G>C c.493G>C c.(493-495)Gaa>Caa p.E165Q BRCA 16 68842433 68842433 + Frame_Shift_Del DEL A A - TCGA-A8-A09V-01A-11D-A045-09 TCGA-A8-A09V-10A-01W-A055-09 g.chr16:68842433delA c.494delA c.(493-495)gaafs p.E165fs BRCA 16 68842433 68842433 + Frame_Shift_Del DEL A A - TCGA-D8-A27I-01A-11D-A16D-09 TCGA-D8-A27I-10A-02D-A16D-09 g.chr16:68842433delA c.494delA c.(493-495)gaafs p.E165fs BRCA 16 68842438 68842439 + Frame_Shift_Ins INS - - A TCGA-D8-A27G-01A-11D-A16D-09 TCGA-D8-A27G-10A-01D-A16D-09 g.chr16:68842438_68842439insA c.499_500insA c.(499-501)gaafs p.E167fs BRCA 16 68842438 68842439 + In_Frame_Ins INS - - CCC TCGA-A8-A09V-01A-11D-A045-09 TCGA-A8-A09V-10A-01W-A055-09 g.chr16:68842438_68842439insCCC c.499_500insCCC c.(499-501)gaa>gCCCaa p.167_167E>AQ BRCA 16 68842603 68842603 + Frame_Shift_Del DEL C C - TCGA-OL-A5DA-01A-11D-A27P-09 TCGA-OL-A5DA-10A-01D-A27P-09 g.chr16:68842603delC c.539delC c.(538-540)tccfs p.S180fs BRCA 16 68842647 68842647 + Nonsense_Mutation SNP C C T TCGA-AC-A3TN-01A-11D-A228-09 TCGA-AC-A3TN-10A-01D-A22A-09 g.chr16:68842647C>T c.583C>T c.(583-585)Caa>Taa p.Q195* BRCA 16 68842647 68842647 + Nonsense_Mutation SNP C C T TCGA-B6-A2IU-01A-32D-A19T-09 TCGA-B6-A2IU-10A-01D-A18P-09 g.chr16:68842647C>T c.583C>T c.(583-585)Caa>Taa p.Q195* BRCA 16 68842658 68842659 + Frame_Shift_Ins INS - - A TCGA-AC-A3W7-01A-11D-A228-09 TCGA-AC-A3W7-10A-01D-A22A-09 g.chr16:68842658_68842659insA c.594_595insA c.(595-597)acafs p.T199fs BRCA 16 68842661 68842662 + Frame_Shift_Ins INS - - C TCGA-AC-A2FG-01A-11D-A17D-09 TCGA-AC-A2FG-11A-22D-A17D-09 g.chr16:68842661_68842662insC c.597_598insC c.(598-600)cccfs p.P200fs BRCA 16 68842662 68842662 + Frame_Shift_Del DEL C C - TCGA-A8-A07B-01A-11W-A019-09 TCGA-A8-A07B-10A-01W-A021-09 g.chr16:68842662delC c.598delC c.(598-600)cccfs p.P201fs BRCA 16 68842664 68842665 + Missense_Mutation DNP CC CC AG TCGA-A8-A07B-01A-11W-A019-09 TCGA-A8-A07B-10A-01W-A021-09 g.chr16:68842664_68842665CC>AG c.600_601CC>AG c.(598-603)ccCCct>ccAGct p.P201A BRCA 16 68842676 68842677 + Frame_Shift_Ins INS - - T TCGA-E2-A2P6-01A-11D-A19Y-09 TCGA-E2-A2P6-10B-01D-A19Y-09 g.chr16:68842676_68842677insT c.612_613insT c.(613-615)tttfs p.F205fs BRCA 16 68844099 68844099 + Splice_Site SNP G G A TCGA-BH-A0HP-01A-12D-A099-09 TCGA-BH-A0HP-10A-01D-A099-09 g.chr16:68844099G>A c.e6-1 BRCA 16 68844104 68844105 + Frame_Shift_Del DEL TC TC - TCGA-B6-A0IP-01A-11D-A045-09 TCGA-B6-A0IP-10A-01W-A055-09 g.chr16:68844104_68844105delTC c.692_693delTC c.(691-693)ttcfs p.F231fs BRCA 16 68844139 68844139 + Missense_Mutation SNP G G A TCGA-A1-A0SE-01A-11D-A099-09 TCGA-A1-A0SE-10A-03D-A099-09 g.chr16:68844139G>A c.727G>A c.(727-729)Gag>Aag p.E243K BRCA 16 68844139 68844139 + Missense_Mutation SNP G G A TCGA-A8-A091-01A-11W-A019-09 TCGA-A8-A091-10A-01W-A021-09 g.chr16:68844139G>A c.727G>A c.(727-729)Gag>Aag p.E243K BRCA 16 68844139 68844139 + Missense_Mutation SNP G G A TCGA-A8-A0A7-01A-11W-A019-09 TCGA-A8-A0A7-10A-01W-A021-09 g.chr16:68844139G>A c.727G>A c.(727-729)Gag>Aag p.E243K BRCA 16 68844164 68844164 + Missense_Mutation SNP C C A TCGA-GM-A2DD-01A-11D-A17W-09 TCGA-GM-A2DD-10C-01D-A17W-09 g.chr16:68844164C>A c.752C>A c.(751-753)aCg>aAg p.T251K BRCA 16 68844175 68844175 + Nonsense_Mutation SNP C C T TCGA-AR-A2LE-01A-11D-A17W-09 TCGA-AR-A2LE-10A-01D-A17W-09 g.chr16:68844175C>T c.763C>T c.(763-765)Cag>Tag p.Q255* BRCA 16 68844191 68844191 + Missense_Mutation SNP C C A TCGA-BH-A0BA-01A-11W-A071-09 TCGA-BH-A0BA-11A-22W-A100-09 g.chr16:68844191C>A c.779C>A c.(778-780)cCc>cAc p.P260H BRCA 16 68844244 68844244 + Splice_Site SNP G G A TCGA-AR-A2LL-01A-11D-A17W-09 TCGA-AR-A2LL-10A-01D-A17W-09 g.chr16:68844244G>A c.832G>A c.(832-834)Gga>Aga p.G278R BRCA 16 68844244 68844244 + Splice_Site SNP G G T TCGA-A2-A0CK-01A-11D-A228-09 TCGA-A2-A0CK-10A-01D-A22A-09 g.chr16:68844244G>T c.832G>T c.(832-834)Gga>Tga p.G278* BRCA 16 68844245 68844245 + Splice_Site SNP G G A TCGA-E2-A1L8-01A-11D-A13L-09 TCGA-E2-A1L8-10A-01D-A13O-09 g.chr16:68844245G>A c.e6+1 BRCA 16 68845587 68845587 + Splice_Site SNP G G T TCGA-PE-A5DE-01A-11D-A27P-09 TCGA-PE-A5DE-10A-01D-A27P-09 g.chr16:68845587G>T c.833G>T c.(832-834)gGa>gTa p.G278V BRCA 16 68845600 68845600 + Missense_Mutation SNP G G T TCGA-AC-A3W6-01A-12D-A228-09 TCGA-AC-A3W6-10A-01D-A22A-09 g.chr16:68845600G>T c.846G>T c.(844-846)atG>atT p.M282I BRCA 16 68845616 68845616 + Missense_Mutation SNP G G A TCGA-GM-A2DO-01A-11D-A19Y-09 TCGA-GM-A2DO-10D-01D-A18P-09 g.chr16:68845616G>A c.862G>A c.(862-864)Gac>Aac p.D288N BRCA 16 68845617 68845618 + Frame_Shift_Del DEL AC AC - TCGA-A7-A4SC-01A-12D-A25Q-09 TCGA-A7-A4SC-10A-01D-A25Q-09 g.chr16:68845617_68845618delAC c.863_864delAC c.(862-864)gacfs p.D288fs BRCA 16 68845625 68845625 + Frame_Shift_Del DEL G G - TCGA-A8-A09X-01A-11W-A019-09 TCGA-A8-A09X-10A-01W-A021-09 g.chr16:68845625delG c.871delG c.(871-873)gatfs p.D292fs BRCA 16 68845663 68845664 + Frame_Shift_Ins INS - - A TCGA-GM-A5PX-01A-12D-A28B-09 TCGA-GM-A5PX-10A-01D-A28E-09 g.chr16:68845663_68845664insA c.909_910insA c.(910-912)atcfs p.I304fs BRCA 16 68845685 68845686 + Frame_Shift_Ins INS - - T TCGA-E2-A10F-01A-11D-A10M-09 TCGA-E2-A10F-10A-01D-A10M-09 g.chr16:68845685_68845686insT c.931_932insT c.(931-933)ctcfs p.L311fs BRCA 16 68845694 68845694 + Frame_Shift_Del DEL A A - TCGA-AR-A1AT-01A-11D-A12Q-09 TCGA-AR-A1AT-10A-01D-A12Q-09 g.chr16:68845694delA c.940delA c.(940-942)aaafs p.K314fs BRCA 16 68845757 68845757 + Nonsense_Mutation SNP C C T TCGA-A2-A0CO-01A-13D-A228-09 TCGA-A2-A0CO-10A-01D-A22A-09 g.chr16:68845757C>T c.1003C>T c.(1003-1005)Cga>Tga p.R335* BRCA 16 68845757 68845757 + Nonsense_Mutation SNP C C T TCGA-A7-A3IZ-01A-11D-A20S-09 TCGA-A7-A3IZ-10A-01D-A20S-09 g.chr16:68845757C>T c.1003C>T c.(1003-1005)Cga>Tga p.R335* BRCA 16 68845757 68845757 + Nonsense_Mutation SNP C C T TCGA-PE-A5DD-01A-12D-A27P-09 TCGA-PE-A5DD-10A-01D-A27P-09 g.chr16:68845757C>T c.1003C>T c.(1003-1005)Cga>Tga p.R335* BRCA 16 68845762 68845762 + Splice_Site SNP G G A TCGA-E2-A107-01A-11D-A10M-09 TCGA-E2-A107-10A-01D-A10M-09 g.chr16:68845762G>A c.1008G>A c.(1006-1008)gaG>gaA p.E336E BRCA 16 68846043 68846043 + Frame_Shift_Del DEL C C - TCGA-A2-A0YD-01A-11D-A10G-09 TCGA-A2-A0YD-10A-01D-A10G-09 g.chr16:68846043delC c.1014delC c.(1012-1014)ttcfs p.F338fs BRCA 16 68846048 68846049 + Frame_Shift_Ins INS - - G TCGA-C8-A3M7-01A-12D-A21Q-09 TCGA-C8-A3M7-10A-01D-A21Q-09 g.chr16:68846048_68846049insG c.1019_1020insG c.(1018-1023)acgtatfs p.Y341fs BRCA 16 68846065 68846065 + Nonsense_Mutation SNP C C T TCGA-AC-A23G-01A-11D-A20S-09 TCGA-AC-A23G-11A-12D-A20S-09 g.chr16:68846065C>T c.1036C>T c.(1036-1038)Caa>Taa p.Q346* BRCA 16 68846166 68846166 + Splice_Site SNP G G A TCGA-D8-A27T-01A-11D-A16D-09 TCGA-D8-A27T-10A-01D-A16D-09 g.chr16:68846166G>A c.1137G>A c.(1135-1137)acG>acA p.T379T BRCA 16 68847225 68847225 + Nonsense_Mutation SNP C C T TCGA-E2-A2P5-01A-11D-A19Y-09 TCGA-E2-A2P5-10B-01D-A19Y-09 g.chr16:68847225C>T c.1147C>T c.(1147-1149)Cag>Tag p.Q383* BRCA 16 68847278 68847279 + Frame_Shift_Ins INS - - A TCGA-A8-A0AB-01A-11W-A050-09 TCGA-A8-A0AB-10A-01W-A055-09 g.chr16:68847278_68847279insA c.1200_1201insA c.(1201-1203)gctfs p.A401fs BRCA 16 68847282 68847282 + Missense_Mutation SNP G G C TCGA-E9-A2JT-01A-22D-A18P-09 TCGA-E9-A2JT-10A-01D-A18P-09 g.chr16:68847282G>C c.1204G>C c.(1204-1206)Gat>Cat p.D402H BRCA 16 68847304 68847304 + Missense_Mutation SNP G G T TCGA-GI-A2C8-01A-11D-A16D-09 TCGA-GI-A2C8-11A-22D-A16D-09 g.chr16:68847304G>T c.1226G>T c.(1225-1227)tGg>tTg p.W409L BRCA 16 68847304 68847304 + Nonsense_Mutation SNP G G A TCGA-LQ-A4E4-01A-11D-A25Q-09 TCGA-LQ-A4E4-10A-01D-A25Q-09 g.chr16:68847304G>A c.1226G>A c.(1225-1227)tGg>tAg p.W409* BRCA 16 68847369 68847370 + Frame_Shift_Del DEL AA AA - TCGA-D8-A3Z6-01A-11D-A23C-09 TCGA-D8-A3Z6-10A-01D-A23C-09 g.chr16:68847369_68847370delAA c.1291_1292delAA c.(1291-1293)aacfs p.N432fs BRCA 16 68849436 68849436 + Nonsense_Mutation SNP A A T TCGA-MS-A51U-01A-31D-A25Q-09 TCGA-MS-A51U-10A-01D-A25Q-09 g.chr16:68849436A>T c.1339A>T c.(1339-1341)Aag>Tag p.K447* BRCA 16 68849577 68849577 + Nonsense_Mutation SNP G G T TCGA-B6-A40B-01A-11D-A23C-09 TCGA-B6-A40B-10A-01D-A23C-09 g.chr16:68849577G>T c.1480G>T c.(1480-1482)Gaa>Taa p.E494* BRCA 16 68849593 68849594 + Frame_Shift_Ins INS - - G TCGA-EW-A1J5-01A-11D-A13L-09 TCGA-EW-A1J5-10A-01D-A13O-09 g.chr16:68849593_68849594insG c.1496_1497insG c.(1495-1500)tttggcfs p.FG499fs BRCA 16 68849604 68849604 + Nonsense_Mutation SNP C C T TCGA-A8-A0A9-01A-11W-A019-09 TCGA-A8-A0A9-10A-01W-A021-09 g.chr16:68849604C>T c.1507C>T c.(1507-1509)Cag>Tag p.Q503* BRCA 16 68849608 68849608 + Frame_Shift_Del DEL A A - TCGA-AR-A1AL-01A-21D-A12Q-09 TCGA-AR-A1AL-10A-01D-A12Q-09 g.chr16:68849608delA c.1511delA c.(1510-1512)gaafs p.E504fs BRCA 16 68849628 68849628 + Nonsense_Mutation SNP C C T TCGA-A2-A0EX-01A-21W-A050-09 TCGA-A2-A0EX-10A-01W-A055-09 g.chr16:68849628C>T c.1531C>T c.(1531-1533)Cag>Tag p.Q511* BRCA 16 68849631 68849631 + Nonsense_Mutation SNP G G T TCGA-OL-A5RV-01A-12D-A28B-09 TCGA-OL-A5RV-10A-01D-A28E-09 g.chr16:68849631G>T c.1534G>T c.(1534-1536)Gag>Tag p.E512* BRCA 16 68849641 68849642 + In_Frame_Ins INS - - ATA TCGA-E9-A3X8-01A-31D-A22X-09 TCGA-E9-A3X8-10B-01D-A22X-09 g.chr16:68849641_68849642insATA c.1544_1545insATA c.(1543-1548)acattt>acATAattt p.515_516TF>T*F BRCA 16 68849648 68849648 + Frame_Shift_Del DEL G G - TCGA-AO-A0J9-01A-11W-A050-09 TCGA-AO-A0J9-10A-01W-A055-09 g.chr16:68849648delG c.1551delG c.(1549-1551)atgfs p.M517fs BRCA 16 68849663 68849663 + Splice_Site SNP G G A TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr16:68849663G>A c.e10+1 BRCA 16 68855914 68855915 + Frame_Shift_Ins INS - - G TCGA-OL-A66K-01A-11D-A29N-09 TCGA-OL-A66K-10A-01D-A29N-09 g.chr16:68855914_68855915insG c.1722_1723insG c.(1723-1725)gctfs p.A575fs BRCA 16 68855935 68855936 + Frame_Shift_Ins INS - - CTGC TCGA-BH-A18F-01A-11D-A12B-09 TCGA-BH-A18F-11A-22D-A12B-09 g.chr16:68855935_68855936insCTGC c.1743_1744insCTGC c.(1744-1746)ctgfs p.-582fs BRCA 16 68855995 68855996 + Frame_Shift_Ins INS - - T TCGA-A7-A4SB-01A-21D-A25Q-09 TCGA-A7-A4SB-10A-01D-A25Q-09 g.chr16:68855995_68855996insT c.1803_1804insT c.(1804-1806)ttcfs p.F602fs BRCA 16 68856011 68856011 + Missense_Mutation SNP C C T TCGA-E2-A1IH-01A-11D-A188-09 TCGA-E2-A1IH-10A-01D-A13O-09 g.chr16:68856011C>T c.1819C>T c.(1819-1821)Cca>Tca p.P607S BRCA 16 68856067 68856068 + Frame_Shift_Ins INS - - T TCGA-C8-A274-01A-11D-A16D-09 TCGA-C8-A274-10A-01D-A16D-09 g.chr16:68856067_68856068insT c.1875_1876insT c.(1876-1878)ttcfs p.F626fs BRCA 16 68856094 68856094 + Silent SNP G G A TCGA-PE-A5DC-01A-12D-A27P-09 TCGA-PE-A5DC-10A-01D-A27P-09 g.chr16:68856094G>A c.1902G>A c.(1900-1902)gcG>gcA p.A634A BRCA 16 68856113 68856113 + Nonsense_Mutation SNP C C T TCGA-AC-A3OD-01A-11D-A21Q-09 TCGA-AC-A3OD-10A-01D-A21Q-09 g.chr16:68856113C>T c.1921C>T c.(1921-1923)Cag>Tag p.Q641* BRCA 16 68856122 68856122 + Missense_Mutation SNP G G A TCGA-C8-A1HO-01A-11D-A13L-09 TCGA-C8-A1HO-10A-01D-A188-09 g.chr16:68856122G>A c.1930G>A c.(1930-1932)Gac>Aac p.D644N BRCA 16 68856129 68856129 + Splice_Site SNP G G A TCGA-A8-A09W-01A-11W-A019-09 TCGA-A8-A09W-10A-01W-A021-09 g.chr16:68856129G>A c.e12+1 BRCA 16 68856129 68856129 + Splice_Site SNP G G T TCGA-D8-A1Y1-01A-21D-A14K-09 TCGA-D8-A1Y1-10A-01D-A14K-09 g.chr16:68856129G>T c.e12+1 BRCA 16 68857311 68857312 + Frame_Shift_Ins INS - - T TCGA-AR-A24T-01A-11D-A167-09 TCGA-AR-A24T-10A-01D-A167-09 g.chr16:68857311_68857312insT c.1946_1947insT c.(1945-1950)tctatcfs p.I650fs BRCA 16 68857367 68857367 + Nonsense_Mutation SNP A A T TCGA-EW-A1J2-01A-21D-A13L-09 TCGA-EW-A1J2-10A-01W-A14R-09 g.chr16:68857367A>T c.2002A>T c.(2002-2004)Aag>Tag p.K668* BRCA 16 68857397 68857398 + Frame_Shift_Ins INS - - T TCGA-E2-A1IJ-01A-11D-A142-09 TCGA-E2-A1IJ-10A-01D-A142-09 g.chr16:68857397_68857398insT c.2032_2033insT c.(2032-2034)gtgfs p.V678fs BRCA 16 68857485 68857485 + Frame_Shift_Del DEL T T - TCGA-AO-A0J8-01A-21D-A045-09 TCGA-AO-A0J8-10A-01W-A055-09 g.chr16:68857485delT c.2120delT c.(2119-2121)attfs p.I707fs BRCA 16 68857496 68857496 + Frame_Shift_Del DEL C C - TCGA-A7-A3J1-01A-11D-A20S-09 TCGA-A7-A3J1-10A-01D-A20S-09 g.chr16:68857496delC c.2131delC c.(2131-2133)ctgfs p.L711fs BRCA 16 68857527 68857530 + Splice_Site DEL TAAG TAAG - TCGA-EW-A3E8-01B-11D-A243-09 TCGA-EW-A3E8-10A-01D-A243-09 g.chr16:68857527_68857530delTAAG c.2162_2164delTAAG c.(2161-2166)ctaagt>cgt p.LS721fs BRCA 16 68862076 68862076 + Splice_Site SNP G G A TCGA-GM-A5PV-01A-11D-A28B-09 TCGA-GM-A5PV-10A-01D-A28E-09 g.chr16:68862076G>A c.e14-1 BRCA 16 68862076 68862076 + Splice_Site SNP G G T TCGA-AR-A24X-01A-11D-A167-09 TCGA-AR-A24X-10A-01D-A167-09 g.chr16:68862076G>T c.e14-1 BRCA 16 68862095 68862095 + Nonsense_Mutation SNP T T A TCGA-A7-A426-01A-22D-A243-09 TCGA-A7-A426-10A-01D-A243-09 g.chr16:68862095T>A c.2183T>A c.(2182-2184)tTg>tAg p.L728* BRCA 16 68862100 68862103 + Frame_Shift_Del DEL TTTC TTTC - TCGA-AC-A5XS-01A-11D-A29N-09 TCGA-AC-A5XS-10A-01D-A29N-09 g.chr16:68862100_68862103delTTTC c.2188_2191delTTTC c.(2188-2193)tttcttfs p.FL730fs BRCA 16 68862103 68862103 + Frame_Shift_Del DEL C C - TCGA-A7-A5ZX-01A-12D-A29N-09 TCGA-A7-A5ZX-10A-01D-A29N-09 g.chr16:68862103delC c.2191delC c.(2191-2193)cttfs p.L731fs BRCA 16 68862107 68862107 + Missense_Mutation SNP G G A TCGA-A2-A25A-01A-12D-A16D-09 TCGA-A2-A25A-10A-01D-A16D-09 g.chr16:68862107G>A c.2195G>A c.(2194-2196)cGg>cAg p.R732Q BRCA 16 68862109 68862110 + Frame_Shift_Ins INS - - G TCGA-AC-A3TM-01A-11D-A228-09 TCGA-AC-A3TM-10A-01D-A22A-09 g.chr16:68862109_68862110insG c.2197_2198insG c.(2197-2199)aggfs p.R733fs BRCA 16 68862155 68862155 + Frame_Shift_Del DEL C C - TCGA-A2-A3KC-01A-11D-A20S-09 TCGA-A2-A3KC-10A-01D-A20S-09 g.chr16:68862155delC c.2243delC c.(2242-2244)accfs p.T748fs BRCA 16 68862178 68862179 + Frame_Shift_Ins INS - - AT TCGA-BH-A0E9-01B-11D-A10Y-09 TCGA-BH-A0E9-10A-01D-A110-09 g.chr16:68862178_68862179insAT c.2266_2267insAT c.(2266-2268)gatfs p.D756fs BRCA 16 68862179 68862180 + Frame_Shift_Ins INS - - T TCGA-A2-A0T4-01A-31D-A099-09 TCGA-A2-A0T4-10A-01D-A099-09 g.chr16:68862179_68862180insT c.2267_2268insT c.(2266-2271)gatgaafs p.E757fs BRCA 16 68862200 68862201 + Frame_Shift_Ins INS - - G TCGA-AC-A3YI-01A-21D-A23C-09 TCGA-AC-A3YI-10A-01D-A23C-09 g.chr16:68862200_68862201insG c.2288_2289insG c.(2287-2292)gaggacfs p.D764fs BRCA 16 68862203 68862204 + Frame_Shift_Ins INS - - C TCGA-A8-A0A4-01A-11W-A019-09 TCGA-A8-A0A4-10A-01W-A021-09 g.chr16:68862203_68862204insC c.2291_2292insC c.(2290-2295)gaccagfs p.Q765fs BRCA 16 68863630 68863630 + Frame_Shift_Del DEL C C - TCGA-D8-A3Z5-01A-41D-A243-09 TCGA-D8-A3Z5-10A-01D-A243-09 g.chr16:68863630delC c.2369delC c.(2368-2370)accfs p.T790fs BRCA 16 68863661 68863661 + Frame_Shift_Del DEL C C - TCGA-BH-A2L8-01A-11D-A18P-09 TCGA-BH-A2L8-10A-01D-A18P-09 g.chr16:68863661delC c.2400delC c.(2398-2400)cgcfs p.R800fs BRCA 16 68867203 68867203 + Missense_Mutation SNP C C T TCGA-AO-A128-01A-11D-A10M-09 TCGA-AO-A128-10A-01D-A10M-09 g.chr16:68867203C>T c.2450C>T c.(2449-2451)gCg>gTg p.A817V BRCA 16 68867222 68867223 + Frame_Shift_Ins INS - - G TCGA-AC-A2FO-01A-11D-A17W-09 TCGA-AC-A2FO-11A-12D-A17W-09 g.chr16:68867222_68867223insG c.2469_2470insG c.(2470-2472)gccfs p.A824fs BRCA 16 68867233 68867234 + Frame_Shift_Ins INS - - TGAT TCGA-A2-A0T6-01A-11D-A099-09 TCGA-A2-A0T6-10A-01D-A099-09 g.chr16:68867233_68867234insTGAT c.2480_2481insTGAT c.(2479-2484)tatgatfs p.-828fs BRCA 16 68867258 68867258 + Nonsense_Mutation SNP T T A TCGA-A2-A4S2-01A-12D-A25Q-09 TCGA-A2-A4S2-10A-01D-A25Q-09 g.chr16:68867258T>A c.2505T>A c.(2503-2505)taT>taA p.Y835* BRCA 16 68867353 68867353 + Missense_Mutation SNP A A G TCGA-A2-A1G0-01A-11D-A13L-09 TCGA-A2-A1G0-10A-01D-A13O-09 g.chr16:68867353A>G c.2600A>G c.(2599-2601)aAt>aGt p.N867S CESC 16 68862194 68862194 + Missense_Mutation SNP G G A TCGA-JX-A3Q0-01A-11D-A21Q-09 TCGA-JX-A3Q0-10A-01D-A21Q-09 g.chr16:68862194G>A c.2282G>A c.(2281-2283)gGa>gAa p.G761E CESC 16 68867208 68867208 + Missense_Mutation SNP G G A TCGA-IR-A3LH-01A-21D-A20U-09 TCGA-IR-A3LH-10A-01D-A20U-09 g.chr16:68867208G>A c.2455G>A c.(2455-2457)Gat>Aat p.D819N CHOL 16 68835581 68835581 + Missense_Mutation SNP G G C TCGA-ZH-A8Y8-01A-51D-A417-09 TCGA-ZH-A8Y8-10A-01D-A41A-09 g.chr16:68835581G>C c.172G>C c.(172-174)Gaa>Caa p.E58Q COAD 16 68772218 68772218 + Nonsense_Mutation SNP C C T TCGA-CK-4952-01A-01D-1719-10 TCGA-CK-4952-10A-01D-1719-10 g.chr16:68772218C>T c.67C>T c.(67-69)Cag>Tag p.Q23* COAD 16 68772219 68772219 + Missense_Mutation SNP A A G TCGA-CM-6679-01A-11D-1835-10 TCGA-CM-6679-10A-01D-1835-10 g.chr16:68772219A>G c.68A>G c.(67-69)cAg>cGg p.Q23R COAD 16 68772239 68772239 + Missense_Mutation SNP C C T TCGA-CA-6715-01A-21D-1835-10 TCGA-CA-6715-10A-01D-1835-10 g.chr16:68772239C>T c.88C>T c.(88-90)Cct>Tct p.P30S COAD 16 68835582 68835582 + Missense_Mutation SNP A A G TCGA-A6-5659-01A-01D-1650-10 TCGA-A6-5659-11A-01D-1650-10 g.chr16:68835582A>G c.173A>G c.(172-174)gAa>gGa p.E58G COAD 16 68835583 68835583 + Silent SNP A A G TCGA-CM-5349-01A-21D-1719-10 TCGA-CM-5349-10A-01D-1719-10 g.chr16:68835583A>G c.174A>G c.(172-174)gaA>gaG p.E58E COAD 16 68835593 68835593 + Missense_Mutation SNP G G A TCGA-CM-6172-01A-11D-1650-10 TCGA-CM-6172-10A-01D-1650-10 g.chr16:68835593G>A c.184G>A c.(184-186)Ggt>Agt p.G62S COAD 16 68835593 68835593 + Missense_Mutation SNP G G T TCGA-D5-6536-01A-11D-1719-10 TCGA-D5-6536-10A-01D-1719-10 g.chr16:68835593G>T c.184G>T c.(184-186)Ggt>Tgt p.G62C COAD 16 68835595 68835595 + Silent SNP T T C TCGA-CM-4744-01A-01D-1408-10 TCGA-CM-4744-10A-01D-1408-10 g.chr16:68835595T>C c.186T>C c.(184-186)ggT>ggC p.G62G COAD 16 68835629 68835629 + Nonsense_Mutation SNP C C T TCGA-CM-6161-01A-11D-1650-10 TCGA-CM-6161-10A-01D-1650-10 g.chr16:68835629C>T c.220C>T c.(220-222)Cga>Tga p.R74* COAD 16 68835629 68835629 + Nonsense_Mutation SNP C C T TCGA-CM-6170-01A-11D-1650-10 TCGA-CM-6170-10A-01D-1650-10 g.chr16:68835629C>T c.220C>T c.(220-222)Cga>Tga p.R74* COAD 16 68835630 68835630 + Missense_Mutation SNP G G A TCGA-AA-3697-01A-01D-1719-10 TCGA-AA-3697-11A-01D-1719-10 g.chr16:68835630G>A c.221G>A c.(220-222)cGa>cAa p.R74Q COAD 16 68835672 68835672 + Missense_Mutation SNP C C A TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr16:68835672C>A c.263C>A c.(262-264)cCt>cAt p.P88H COAD 16 68835711 68835711 + Missense_Mutation SNP A A G TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr16:68835711A>G c.302A>G c.(301-303)tAc>tGc p.Y101C COAD 16 68835781 68835781 + Frame_Shift_Del DEL C C - TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr16:68835781delC c.372delC c.(370-372)cgcfs p.R124fs COAD 16 68835781 68835781 + Frame_Shift_Del DEL C C - TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr16:68835781delC c.372delC c.(370-372)cgcfs p.R124fs COAD 16 68842333 68842333 + Missense_Mutation SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr16:68842333G>A c.394G>A c.(394-396)Gtt>Att p.V132I COAD 16 68842734 68842734 + Missense_Mutation SNP C C T TCGA-AA-A02K-01A-21W-A096-10 TCGA-AA-A02K-10A-01W-A096-10 g.chr16:68842734C>T c.670C>T c.(670-672)Cgc>Tgc p.R224C COAD 16 68844109 68844109 + Missense_Mutation SNP C C T TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr16:68844109C>T c.697C>T c.(697-699)Cac>Tac p.H233Y COAD 16 68844126 68844126 + Silent SNP C C T TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr16:68844126C>T c.714C>T c.(712-714)aaC>aaT p.N238N COAD 16 68844140 68844140 + Missense_Mutation SNP A A G TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr16:68844140A>G c.728A>G c.(727-729)gAg>gGg p.E243G COAD 16 68844145 68844145 + Missense_Mutation SNP C C T TCGA-CM-5348-01A-21D-1719-10 TCGA-CM-5348-10A-01D-1719-10 g.chr16:68844145C>T c.733C>T c.(733-735)Cca>Tca p.P245S COAD 16 68844146 68844146 + Missense_Mutation SNP C C T TCGA-D5-6529-01A-11D-1771-10 TCGA-D5-6529-10A-01D-1771-10 g.chr16:68844146C>T c.734C>T c.(733-735)cCa>cTa p.P245L COAD 16 68844147 68844147 + Silent SNP A A T TCGA-G4-6323-01A-11D-1719-10 TCGA-G4-6323-10A-01D-1720-10 g.chr16:68844147A>T c.735A>T c.(733-735)ccA>ccT p.P245P COAD 16 68844174 68844174 + Silent SNP T T C TCGA-A6-5666-01A-01D-1650-10 TCGA-A6-5666-10A-01D-1650-10 g.chr16:68844174T>C c.762T>C c.(760-762)gaT>gaC p.D254D COAD 16 68844174 68844174 + Silent SNP T T C TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr16:68844174T>C c.762T>C c.(760-762)gaT>gaC p.D254D COAD 16 68844176 68844176 + Missense_Mutation SNP A A T TCGA-G4-6317-01A-11D-1719-10 TCGA-G4-6317-10A-01D-1720-10 g.chr16:68844176A>T c.764A>T c.(763-765)cAg>cTg p.Q255L COAD 16 68844181 68844181 + Missense_Mutation SNP G G A TCGA-F4-6460-01A-11D-1771-10 TCGA-F4-6460-10B-01D-1771-10 g.chr16:68844181G>A c.769G>A c.(769-771)Gac>Aac p.D257N COAD 16 68844183 68844183 + Silent SNP C C T TCGA-AY-5543-01A-01D-1650-10 TCGA-AY-5543-10A-01D-1650-10 g.chr16:68844183C>T c.771C>T c.(769-771)gaC>gaT p.D257D COAD 16 68844192 68844192 + Silent SNP C C A TCGA-AZ-6599-01A-11D-1771-10 TCGA-AZ-6599-11A-01D-1771-10 g.chr16:68844192C>A c.780C>A c.(778-780)ccC>ccA p.P260P COAD 16 68845615 68845615 + Silent SNP A A G TCGA-CM-5348-01A-21D-1719-10 TCGA-CM-5348-10A-01D-1719-10 g.chr16:68845615A>G c.861A>G c.(859-861)acA>acG p.T287T COAD 16 68845620 68845620 + Missense_Mutation SNP C C T TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr16:68845620C>T c.866C>T c.(865-867)gCg>gTg p.A289V COAD 16 68845625 68845625 + Missense_Mutation SNP G G A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr16:68845625G>A c.871G>A c.(871-873)Gat>Aat p.D291N COAD 16 68845638 68845638 + Missense_Mutation SNP C C T TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr16:68845638C>T c.884C>T c.(883-885)aCc>aTc p.T295I COAD 16 68845647 68845647 + Missense_Mutation SNP C C T TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr16:68845647C>T c.893C>T c.(892-894)gCc>gTc p.A298V COAD 16 68845653 68845653 + Missense_Mutation SNP T T C TCGA-AA-A02K-01A-21W-A096-10 TCGA-AA-A02K-10A-01W-A096-10 g.chr16:68845653T>C c.899T>C c.(898-900)aTc>aCc p.I300T COAD 16 68845653 68845653 + Missense_Mutation SNP T T C TCGA-AU-3779-01A-01D-1719-10 TCGA-AU-3779-10A-01D-1719-10 g.chr16:68845653T>C c.899T>C c.(898-900)aTc>aCc p.I300T COAD 16 68845654 68845654 + Silent SNP C C A TCGA-D5-6533-01A-11D-1719-10 TCGA-D5-6533-10A-01D-1719-10 g.chr16:68845654C>A c.900C>A c.(898-900)atC>atA p.I300I COAD 16 68845679 68845679 + Missense_Mutation SNP C C A TCGA-AZ-6600-01A-11D-1771-10 TCGA-AZ-6600-11A-01D-1771-10 g.chr16:68845679C>A c.925C>A c.(925-927)Cct>Act p.P309T COAD 16 68845693 68845694 + Frame_Shift_Ins INS - - A TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr16:68845693_68845694insA c.939_940insA c.(940-942)aaafs p.K314fs COAD 16 68845757 68845757 + Nonsense_Mutation SNP C C T TCGA-AA-A00U-01A-01W-A005-10 TCGA-AA-A00U-10A-01W-A005-10 g.chr16:68845757C>T c.1003C>T c.(1003-1005)Cga>Tga p.R335* COAD 16 68846036 68846036 + Splice_Site SNP A A G TCGA-CK-5915-01A-11D-1650-10 TCGA-CK-5915-10A-01D-1650-10 g.chr16:68846036A>G c.e8-1 COAD 16 68846047 68846047 + Missense_Mutation SNP A A G TCGA-AZ-4616-01A-21D-1835-10 TCGA-AZ-4616-10A-01D-1835-10 g.chr16:68846047A>G c.1018A>G c.(1018-1020)Acg>Gcg p.T340A COAD 16 68846047 68846047 + Missense_Mutation SNP A A G TCGA-D5-6932-01A-11D-1924-10 TCGA-D5-6932-10A-01D-1924-10 g.chr16:68846047A>G c.1018A>G c.(1018-1020)Acg>Gcg p.T340A COAD 16 68846048 68846048 + Missense_Mutation SNP C C G TCGA-DM-A28F-01A-11D-A16V-10 TCGA-DM-A28F-10A-01D-A16V-10 g.chr16:68846048C>G c.1019C>G c.(1018-1020)aCg>aGg p.T340R COAD 16 68846056 68846056 + Missense_Mutation SNP C C A TCGA-AZ-6599-01A-11D-1771-10 TCGA-AZ-6599-11A-01D-1771-10 g.chr16:68846056C>A c.1027C>A c.(1027-1029)Ctg>Atg p.L343M COAD 16 68846069 68846069 + Missense_Mutation SNP C C A TCGA-A6-6648-01A-11D-1771-10 TCGA-A6-6648-10A-01D-1771-10 g.chr16:68846069C>A c.1040C>A c.(1039-1041)gCt>gAt p.A347D COAD 16 68846086 68846086 + Missense_Mutation SNP G G A TCGA-G4-6323-01A-11D-1719-10 TCGA-G4-6323-10A-01D-1720-10 g.chr16:68846086G>A c.1057G>A c.(1057-1059)Gag>Aag p.E353K COAD 16 68846087 68846087 + Missense_Mutation SNP A A G TCGA-A6-3809-01A-01W-0995-10 TCGA-A6-3809-11A-01W-0995-10 g.chr16:68846087A>G c.1058A>G c.(1057-1059)gAg>gGg p.E353G COAD 16 68846087 68846087 + Missense_Mutation SNP A A G TCGA-CA-5797-01A-01D-1650-10 TCGA-CA-5797-10A-01D-1650-10 g.chr16:68846087A>G c.1058A>G c.(1057-1059)gAg>gGg p.E353G COAD 16 68846087 68846087 + Missense_Mutation SNP A A G TCGA-CK-5912-01A-11D-1650-10 TCGA-CK-5912-10A-01D-1650-10 g.chr16:68846087A>G c.1058A>G c.(1057-1059)gAg>gGg p.E353G COAD 16 68846087 68846087 + Missense_Mutation SNP A A G TCGA-CK-5914-01A-11D-1650-10 TCGA-CK-5914-10A-01D-1650-10 g.chr16:68846087A>G c.1058A>G c.(1057-1059)gAg>gGg p.E353G COAD 16 68846087 68846087 + Missense_Mutation SNP A A G TCGA-CM-6678-01A-11D-1835-10 TCGA-CM-6678-10A-01D-1835-10 g.chr16:68846087A>G c.1058A>G c.(1057-1059)gAg>gGg p.E353G COAD 16 68846087 68846087 + Missense_Mutation SNP A A G TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr16:68846087A>G c.1058A>G c.(1057-1059)gAg>gGg p.E353G COAD 16 68846087 68846087 + Missense_Mutation SNP A A G TCGA-DM-A1HA-01A-11D-A152-10 TCGA-DM-A1HA-10A-01D-A152-10 g.chr16:68846087A>G c.1058A>G c.(1057-1059)gAg>gGg p.E353G COAD 16 68846088 68846088 + Silent SNP G G A TCGA-DM-A1D7-01A-11D-A152-10 TCGA-DM-A1D7-10A-01D-A152-10 g.chr16:68846088G>A c.1059G>A c.(1057-1059)gaG>gaA p.E353E COAD 16 68846098 68846098 + Missense_Mutation SNP A A G TCGA-AA-3502-01A-01D-1408-10 TCGA-AA-3502-11A-01D-1408-10 g.chr16:68846098A>G c.1069A>G c.(1069-1071)Aca>Gca p.T357A COAD 16 68846099 68846099 + Missense_Mutation SNP C C A TCGA-DM-A28E-01A-11D-A16V-10 TCGA-DM-A28E-10A-01D-A16V-10 g.chr16:68846099C>A c.1070C>A c.(1069-1071)aCa>aAa p.T357K COAD 16 68846118 68846119 + Frame_Shift_Del DEL CA CA - TCGA-CK-6747-01A-11D-1835-10 TCGA-CK-6747-10A-01D-1835-10 g.chr16:68846118_68846119delCA c.1089_1090delCA c.(1087-1092)atcacafs p.T364fs COAD 16 68846122 68846122 + Missense_Mutation SNP G G A TCGA-AA-3821-01A-01W-0995-10 TCGA-AA-3821-10A-01W-0995-10 g.chr16:68846122G>A c.1093G>A c.(1093-1095)Gtc>Atc p.V365I COAD 16 68846123 68846123 + Missense_Mutation SNP T T C TCGA-G4-6304-01A-11D-1924-10 TCGA-G4-6304-10A-01D-1924-10 g.chr16:68846123T>C c.1094T>C c.(1093-1095)gTc>gCc p.V365A COAD 16 68846135 68846135 + Missense_Mutation SNP A A G TCGA-A6-6141-01A-11D-1771-10 TCGA-A6-6141-10A-01D-1771-10 g.chr16:68846135A>G c.1106A>G c.(1105-1107)aAc>aGc p.N369S COAD 16 68847235 68847235 + Missense_Mutation SNP A A G TCGA-CM-5349-01A-21D-1719-10 TCGA-CM-5349-10A-01D-1719-10 g.chr16:68847235A>G c.1157A>G c.(1156-1158)gAg>gGg p.E386G COAD 16 68847277 68847277 + Missense_Mutation SNP A A G TCGA-CK-4950-01A-01D-1719-10 TCGA-CK-4950-10A-01D-1719-10 g.chr16:68847277A>G c.1199A>G c.(1198-1200)gAt>gGt p.D400G COAD 16 68847283 68847283 + Missense_Mutation SNP A A G TCGA-D5-6536-01A-11D-1719-10 TCGA-D5-6536-10A-01D-1719-10 g.chr16:68847283A>G c.1205A>G c.(1204-1206)gAt>gGt p.D402G COAD 16 68847302 68847302 + Silent SNP G G A TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr16:68847302G>A c.1224G>A c.(1222-1224)gcG>gcA p.A408A COAD 16 68847361 68847361 + Missense_Mutation SNP A A G TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr16:68847361A>G c.1283A>G c.(1282-1284)aAt>aGt p.N428S COAD 16 68849464 68849464 + Missense_Mutation SNP T T C TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr16:68849464T>C c.1367T>C c.(1366-1368)gTg>gCg p.V456A COAD 16 68849484 68849484 + Nonsense_Mutation SNP G G T TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr16:68849484G>T c.1387G>T c.(1387-1389)Gag>Tag p.E463* COAD 16 68849532 68849532 + Missense_Mutation SNP G G T TCGA-D5-6539-01A-11D-1719-10 TCGA-D5-6539-10A-01D-1719-10 g.chr16:68849532G>T c.1435G>T c.(1435-1437)Gat>Tat p.D479Y COAD 16 68849532 68849532 + Missense_Mutation SNP G G T TCGA-DM-A28F-01A-11D-A16V-10 TCGA-DM-A28F-10A-01D-A16V-10 g.chr16:68849532G>T c.1435G>T c.(1435-1437)Gat>Tat p.D479Y COAD 16 68849625 68849625 + Missense_Mutation SNP G G A TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr16:68849625G>A c.1528G>A c.(1528-1530)Gcc>Acc p.A510T COAD 16 68849661 68849661 + Splice_Site SNP A A G TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr16:68849661A>G c.1564A>G c.(1564-1566)Aca>Gca p.T522A COAD 16 68849661 68849661 + Splice_Site SNP A A G TCGA-G4-6321-01A-11D-1719-10 TCGA-G4-6321-10A-01D-1720-10 g.chr16:68849661A>G c.1564A>G c.(1564-1566)Aca>Gca p.T522A COAD 16 68849663 68849663 + Splice_Site SNP G G A TCGA-A6-5657-01A-01D-1650-10 TCGA-A6-5657-10A-01D-1650-10 g.chr16:68849663G>A c.e10+1 COAD 16 68849663 68849663 + Splice_Site SNP G G A TCGA-AA-3697-01A-01D-1719-10 TCGA-AA-3697-11A-01D-1719-10 g.chr16:68849663G>A c.e10+1 COAD 16 68849663 68849663 + Splice_Site SNP G G A TCGA-CM-5868-01A-01D-1650-10 TCGA-CM-5868-10A-01D-1650-10 g.chr16:68849663G>A c.e10+1 COAD 16 68849663 68849663 + Splice_Site SNP G G A TCGA-D5-6539-01A-11D-1719-10 TCGA-D5-6539-10A-01D-1719-10 g.chr16:68849663G>A c.e10+1 COAD 16 68853211 68853211 + Missense_Mutation SNP T T C TCGA-D5-6537-01A-11D-1719-10 TCGA-D5-6537-10A-01D-1719-10 g.chr16:68853211T>C c.1594T>C c.(1594-1596)Tgg>Cgg p.W532R COAD 16 68853294 68853294 + Silent SNP C C T TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr16:68853294C>T c.1677C>T c.(1675-1677)agC>agT p.S559S COAD 16 68853328 68853328 + Splice_Site SNP G G A TCGA-CM-6161-01A-11D-1650-10 TCGA-CM-6161-10A-01D-1650-10 g.chr16:68853328G>A c.1711G>A c.(1711-1713)Ggt>Agt p.G571S COAD 16 68853330 68853330 + Splice_Site SNP T T A TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr16:68853330T>A c.e11+2 COAD 16 68853330 68853330 + Splice_Site SNP T T A TCGA-CM-5344-01A-21D-1719-10 TCGA-CM-5344-10A-01D-1719-10 g.chr16:68853330T>A c.e11+2 COAD 16 68853330 68853330 + Splice_Site SNP T T A TCGA-D5-6932-01A-11D-1924-10 TCGA-D5-6932-10A-01D-1924-10 g.chr16:68853330T>A c.e11+2 COAD 16 68853330 68853330 + Splice_Site SNP T T C TCGA-G4-6310-01A-11D-1719-10 TCGA-G4-6310-10A-01D-1720-10 g.chr16:68853330T>C c.e11+2 COAD 16 68855984 68855984 + Nonsense_Mutation SNP C C T TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr16:68855984C>T c.1792C>T c.(1792-1794)Cga>Tga p.R598* COAD 16 68855984 68855984 + Nonsense_Mutation SNP C C T TCGA-AY-6386-01A-21D-1719-10 TCGA-AY-6386-10A-01D-1719-10 g.chr16:68855984C>T c.1792C>T c.(1792-1794)Cga>Tga p.R598* COAD 16 68855987 68855987 + Missense_Mutation SNP A A G TCGA-D5-6535-01A-11D-1719-10 TCGA-D5-6535-10A-01D-1719-10 g.chr16:68855987A>G c.1795A>G c.(1795-1797)Act>Gct p.T599A COAD 16 68855987 68855987 + Missense_Mutation SNP A A G TCGA-D5-6539-01A-11D-1719-10 TCGA-D5-6539-10A-01D-1719-10 g.chr16:68855987A>G c.1795A>G c.(1795-1797)Act>Gct p.T599A COAD 16 68855988 68855988 + Missense_Mutation SNP C C T TCGA-DM-A282-01A-12D-A16V-10 TCGA-DM-A282-10A-01D-A16V-10 g.chr16:68855988C>T c.1796C>T c.(1795-1797)aCt>aTt p.T599I COAD 16 68855990 68855990 + Missense_Mutation SNP A A G TCGA-D5-6537-01A-11D-1719-10 TCGA-D5-6537-10A-01D-1719-10 g.chr16:68855990A>G c.1798A>G c.(1798-1800)Ata>Gta p.I600V COAD 16 68856041 68856041 + Missense_Mutation SNP G G A TCGA-CM-4752-01A-01D-1408-10 TCGA-CM-4752-10A-01D-1408-10 g.chr16:68856041G>A c.1849G>A c.(1849-1851)Gca>Aca p.A617T COAD 16 68856105 68856105 + Missense_Mutation SNP G G T TCGA-DM-A1D4-01A-21D-A152-10 TCGA-DM-A1D4-10A-01D-A152-10 g.chr16:68856105G>T c.1913G>T c.(1912-1914)tGg>tTg p.W638L COAD 16 68856105 68856105 + Nonsense_Mutation SNP G G A TCGA-AY-6386-01A-21D-1719-10 TCGA-AY-6386-10A-01D-1719-10 g.chr16:68856105G>A c.1913G>A c.(1912-1914)tGg>tAg p.W638* COAD 16 68857418 68857418 + Missense_Mutation SNP G G A TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr16:68857418G>A c.2053G>A c.(2053-2055)Gtg>Atg p.V685M COAD 16 68862096 68862097 + Silent DNP GC GC AT TCGA-AZ-6605-01A-11D-1835-10 TCGA-AZ-6605-11A-01D-1835-10 g.chr16:68862096_68862097GC>AT c.2184_2185GC>AT c.(2182-2187)ttGCtg>ttATtg p.728_729LL>LL COAD 16 68862164 68862164 + Missense_Mutation SNP A A G TCGA-A6-5662-01A-01D-1650-10 TCGA-A6-5662-10A-01D-1650-10 g.chr16:68862164A>G c.2252A>G c.(2251-2253)aAc>aGc p.N751S COAD 16 68862165 68862165 + Silent SNP C C T TCGA-D5-6923-01A-11D-1924-10 TCGA-D5-6923-10A-01D-1924-10 g.chr16:68862165C>T c.2253C>T c.(2251-2253)aaC>aaT p.N751N COAD 16 68863581 68863581 + Missense_Mutation SNP A A G TCGA-AZ-6599-01A-11D-1771-10 TCGA-AZ-6599-11A-01D-1771-10 g.chr16:68863581A>G c.2320A>G c.(2320-2322)Agg>Ggg p.R774G COAD 16 68867265 68867265 + Missense_Mutation SNP A A G TCGA-AA-3662-01A-01D-1719-10 TCGA-AA-3662-11A-01D-1719-10 g.chr16:68867265A>G c.2512A>G c.(2512-2514)Agc>Ggc p.S838G COAD 16 68867265 68867265 + Missense_Mutation SNP A A G TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr16:68867265A>G c.2512A>G c.(2512-2514)Agc>Ggc p.S838G COAD 16 68867267 68867267 + Silent SNP C C T TCGA-CK-4950-01A-01D-1719-10 TCGA-CK-4950-10A-01D-1719-10 g.chr16:68867267C>T c.2514C>T c.(2512-2514)agC>agT p.S838S COAD 16 68867289 68867289 + Missense_Mutation SNP A A G TCGA-G4-6306-01A-11D-1771-10 TCGA-G4-6306-10A-01D-1771-10 g.chr16:68867289A>G c.2536A>G c.(2536-2538)Agc>Ggc p.S846G COAD 16 68867291 68867291 + Silent SNP C C T TCGA-A6-5666-01A-01D-1650-10 TCGA-A6-5666-10A-01D-1650-10 g.chr16:68867291C>T c.2538C>T c.(2536-2538)agC>agT p.S846S COAD 16 68867304 68867304 + Missense_Mutation SNP T T C TCGA-CM-5348-01A-21D-1719-10 TCGA-CM-5348-10A-01D-1719-10 g.chr16:68867304T>C c.2551T>C c.(2551-2553)Tca>Cca p.S851P COAD 16 68867305 68867305 + Nonsense_Mutation SNP C C A TCGA-A6-6141-01A-11D-1771-10 TCGA-A6-6141-10A-01D-1771-10 g.chr16:68867305C>A c.2552C>A c.(2551-2553)tCa>tAa p.S851* COADREAD 16 68772218 68772218 + Nonsense_Mutation SNP C C T TCGA-CK-4952-01A-01D-1719-10 TCGA-CK-4952-10A-01D-1719-10 g.chr16:68772218C>T c.67C>T c.(67-69)Cag>Tag p.Q23* COADREAD 16 68772219 68772219 + Missense_Mutation SNP A A G TCGA-AG-3732-01A-11D-1657-10 TCGA-AG-3732-11A-01D-1657-10 g.chr16:68772219A>G c.68A>G c.(67-69)cAg>cGg p.Q23R COADREAD 16 68772219 68772219 + Missense_Mutation SNP A A G TCGA-CM-6679-01A-11D-1835-10 TCGA-CM-6679-10A-01D-1835-10 g.chr16:68772219A>G c.68A>G c.(67-69)cAg>cGg p.Q23R COADREAD 16 68772239 68772239 + Missense_Mutation SNP C C T TCGA-CA-6715-01A-21D-1835-10 TCGA-CA-6715-10A-01D-1835-10 g.chr16:68772239C>T c.88C>T c.(88-90)Cct>Tct p.P30S COADREAD 16 68835582 68835582 + Missense_Mutation SNP A A G TCGA-A6-5659-01A-01D-1650-10 TCGA-A6-5659-11A-01D-1650-10 g.chr16:68835582A>G c.173A>G c.(172-174)gAa>gGa p.E58G COADREAD 16 68835583 68835583 + Silent SNP A A G TCGA-CM-5349-01A-21D-1719-10 TCGA-CM-5349-10A-01D-1719-10 g.chr16:68835583A>G c.174A>G c.(172-174)gaA>gaG p.E58E COADREAD 16 68835593 68835593 + Missense_Mutation SNP G G A TCGA-CM-6172-01A-11D-1650-10 TCGA-CM-6172-10A-01D-1650-10 g.chr16:68835593G>A c.184G>A c.(184-186)Ggt>Agt p.G62S COADREAD 16 68835593 68835593 + Missense_Mutation SNP G G T TCGA-D5-6536-01A-11D-1719-10 TCGA-D5-6536-10A-01D-1719-10 g.chr16:68835593G>T c.184G>T c.(184-186)Ggt>Tgt p.G62C COADREAD 16 68835595 68835595 + Silent SNP T T C TCGA-CM-4744-01A-01D-1408-10 TCGA-CM-4744-10A-01D-1408-10 g.chr16:68835595T>C c.186T>C c.(184-186)ggT>ggC p.G62G COADREAD 16 68835629 68835629 + Nonsense_Mutation SNP C C T TCGA-CM-6161-01A-11D-1650-10 TCGA-CM-6161-10A-01D-1650-10 g.chr16:68835629C>T c.220C>T c.(220-222)Cga>Tga p.R74* COADREAD 16 68835629 68835629 + Nonsense_Mutation SNP C C T TCGA-CM-6170-01A-11D-1650-10 TCGA-CM-6170-10A-01D-1650-10 g.chr16:68835629C>T c.220C>T c.(220-222)Cga>Tga p.R74* COADREAD 16 68835630 68835630 + Missense_Mutation SNP G G A TCGA-AA-3697-01A-01D-1719-10 TCGA-AA-3697-11A-01D-1719-10 g.chr16:68835630G>A c.221G>A c.(220-222)cGa>cAa p.R74Q COADREAD 16 68835630 68835630 + Missense_Mutation SNP G G A TCGA-G5-6235-01A-11D-1733-10 TCGA-G5-6235-10A-01D-1733-10 g.chr16:68835630G>A c.221G>A c.(220-222)cGa>cAa p.R74Q COADREAD 16 68835672 68835672 + Missense_Mutation SNP C C A TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr16:68835672C>A c.263C>A c.(262-264)cCt>cAt p.P88H COADREAD 16 68835711 68835711 + Missense_Mutation SNP A A G TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr16:68835711A>G c.302A>G c.(301-303)tAc>tGc p.Y101C COADREAD 16 68835727 68835727 + Silent SNP C C T TCGA-F5-6811-01A-11D-1826-10 TCGA-F5-6811-10A-01D-1826-10 g.chr16:68835727C>T c.318C>T c.(316-318)acC>acT p.T106T COADREAD 16 68835781 68835781 + Frame_Shift_Del DEL C C - TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr16:68835781delC c.372delC c.(370-372)cgcfs p.R124fs COADREAD 16 68835781 68835781 + Frame_Shift_Del DEL C C - TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr16:68835781delC c.372delC c.(370-372)cgcfs p.R124fs COADREAD 16 68842333 68842333 + Missense_Mutation SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr16:68842333G>A c.394G>A c.(394-396)Gtt>Att p.V132I COADREAD 16 68842734 68842734 + Missense_Mutation SNP C C T TCGA-AA-A02K-01A-21W-A096-10 TCGA-AA-A02K-10A-01W-A096-10 g.chr16:68842734C>T c.670C>T c.(670-672)Cgc>Tgc p.R224C COADREAD 16 68844109 68844109 + Missense_Mutation SNP C C T TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr16:68844109C>T c.697C>T c.(697-699)Cac>Tac p.H233Y COADREAD 16 68844110 68844110 + Missense_Mutation SNP A A G TCGA-EF-5830-01A-01D-1657-10 TCGA-EF-5830-10A-01D-1657-10 g.chr16:68844110A>G c.698A>G c.(697-699)cAc>cGc p.H233R COADREAD 16 68844126 68844126 + Silent SNP C C T TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr16:68844126C>T c.714C>T c.(712-714)aaC>aaT p.N238N COADREAD 16 68844140 68844140 + Missense_Mutation SNP A A G TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr16:68844140A>G c.728A>G c.(727-729)gAg>gGg p.E243G COADREAD 16 68844145 68844145 + Missense_Mutation SNP C C T TCGA-CM-5348-01A-21D-1719-10 TCGA-CM-5348-10A-01D-1719-10 g.chr16:68844145C>T c.733C>T c.(733-735)Cca>Tca p.P245S COADREAD 16 68844146 68844146 + Missense_Mutation SNP C C T TCGA-D5-6529-01A-11D-1771-10 TCGA-D5-6529-10A-01D-1771-10 g.chr16:68844146C>T c.734C>T c.(733-735)cCa>cTa p.P245L COADREAD 16 68844147 68844147 + Silent SNP A A G TCGA-AF-2687-01A-02D-1733-10 TCGA-AF-2687-10A-01D-1733-10 g.chr16:68844147A>G c.735A>G c.(733-735)ccA>ccG p.P245P COADREAD 16 68844147 68844147 + Silent SNP A A T TCGA-G4-6323-01A-11D-1719-10 TCGA-G4-6323-10A-01D-1720-10 g.chr16:68844147A>T c.735A>T c.(733-735)ccA>ccT p.P245P COADREAD 16 68844172 68844172 + Missense_Mutation SNP G G A TCGA-AF-2687-01A-02D-1733-10 TCGA-AF-2687-10A-01D-1733-10 g.chr16:68844172G>A c.760G>A c.(760-762)Gat>Aat p.D254N COADREAD 16 68844174 68844174 + Silent SNP T T C TCGA-A6-5666-01A-01D-1650-10 TCGA-A6-5666-10A-01D-1650-10 g.chr16:68844174T>C c.762T>C c.(760-762)gaT>gaC p.D254D COADREAD 16 68844174 68844174 + Silent SNP T T C TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr16:68844174T>C c.762T>C c.(760-762)gaT>gaC p.D254D COADREAD 16 68844176 68844176 + Missense_Mutation SNP A A T TCGA-G4-6317-01A-11D-1719-10 TCGA-G4-6317-10A-01D-1720-10 g.chr16:68844176A>T c.764A>T c.(763-765)cAg>cTg p.Q255L COADREAD 16 68844181 68844181 + Missense_Mutation SNP G G A TCGA-F4-6460-01A-11D-1771-10 TCGA-F4-6460-10B-01D-1771-10 g.chr16:68844181G>A c.769G>A c.(769-771)Gac>Aac p.D257N COADREAD 16 68844183 68844183 + Silent SNP C C T TCGA-AY-5543-01A-01D-1650-10 TCGA-AY-5543-10A-01D-1650-10 g.chr16:68844183C>T c.771C>T c.(769-771)gaC>gaT p.D257D COADREAD 16 68844192 68844192 + Silent SNP C C A TCGA-AZ-6599-01A-11D-1771-10 TCGA-AZ-6599-11A-01D-1771-10 g.chr16:68844192C>A c.780C>A c.(778-780)ccC>ccA p.P260P COADREAD 16 68845615 68845615 + Silent SNP A A G TCGA-CM-5348-01A-21D-1719-10 TCGA-CM-5348-10A-01D-1719-10 g.chr16:68845615A>G c.861A>G c.(859-861)acA>acG p.T287T COADREAD 16 68845617 68845617 + Missense_Mutation SNP A A G TCGA-AF-6136-01A-11D-1826-10 TCGA-AF-6136-10A-01D-1826-10 g.chr16:68845617A>G c.863A>G c.(862-864)gAc>gGc p.D288G COADREAD 16 68845620 68845620 + Missense_Mutation SNP C C T TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr16:68845620C>T c.866C>T c.(865-867)gCg>gTg p.A289V COADREAD 16 68845625 68845625 + Missense_Mutation SNP G G A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr16:68845625G>A c.871G>A c.(871-873)Gat>Aat p.D291N COADREAD 16 68845638 68845638 + Missense_Mutation SNP C C T TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr16:68845638C>T c.884C>T c.(883-885)aCc>aTc p.T295I COADREAD 16 68845647 68845647 + Missense_Mutation SNP C C T TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr16:68845647C>T c.893C>T c.(892-894)gCc>gTc p.A298V COADREAD 16 68845653 68845653 + Missense_Mutation SNP T T C TCGA-AA-A02K-01A-21W-A096-10 TCGA-AA-A02K-10A-01W-A096-10 g.chr16:68845653T>C c.899T>C c.(898-900)aTc>aCc p.I300T COADREAD 16 68845653 68845653 + Missense_Mutation SNP T T C TCGA-AU-3779-01A-01D-1719-10 TCGA-AU-3779-10A-01D-1719-10 g.chr16:68845653T>C c.899T>C c.(898-900)aTc>aCc p.I300T COADREAD 16 68845654 68845654 + Silent SNP C C A TCGA-D5-6533-01A-11D-1719-10 TCGA-D5-6533-10A-01D-1719-10 g.chr16:68845654C>A c.900C>A c.(898-900)atC>atA p.I300I COADREAD 16 68845679 68845679 + Missense_Mutation SNP C C A TCGA-AZ-6600-01A-11D-1771-10 TCGA-AZ-6600-11A-01D-1771-10 g.chr16:68845679C>A c.925C>A c.(925-927)Cct>Act p.P309T COADREAD 16 68845693 68845694 + Frame_Shift_Ins INS - - A TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr16:68845693_68845694insA c.939_940insA c.(940-942)aaafs p.K314fs COADREAD 16 68845757 68845757 + Nonsense_Mutation SNP C C T TCGA-AA-A00U-01A-01W-A005-10 TCGA-AA-A00U-10A-01W-A005-10 g.chr16:68845757C>T c.1003C>T c.(1003-1005)Cga>Tga p.R335* COADREAD 16 68846036 68846036 + Splice_Site SNP A A G TCGA-AH-6643-01A-11D-1826-10 TCGA-AH-6643-11A-01D-1826-10 g.chr16:68846036A>G c.e8-1 COADREAD 16 68846036 68846036 + Splice_Site SNP A A G TCGA-CK-5915-01A-11D-1650-10 TCGA-CK-5915-10A-01D-1650-10 g.chr16:68846036A>G c.e8-1 COADREAD 16 68846047 68846047 + Missense_Mutation SNP A A G TCGA-AZ-4616-01A-21D-1835-10 TCGA-AZ-4616-10A-01D-1835-10 g.chr16:68846047A>G c.1018A>G c.(1018-1020)Acg>Gcg p.T340A COADREAD 16 68846047 68846047 + Missense_Mutation SNP A A G TCGA-D5-6932-01A-11D-1924-10 TCGA-D5-6932-10A-01D-1924-10 g.chr16:68846047A>G c.1018A>G c.(1018-1020)Acg>Gcg p.T340A COADREAD 16 68846048 68846048 + Missense_Mutation SNP C C G TCGA-DM-A28F-01A-11D-A16V-10 TCGA-DM-A28F-10A-01D-A16V-10 g.chr16:68846048C>G c.1019C>G c.(1018-1020)aCg>aGg p.T340R COADREAD 16 68846056 68846056 + Missense_Mutation SNP C C A TCGA-AZ-6599-01A-11D-1771-10 TCGA-AZ-6599-11A-01D-1771-10 g.chr16:68846056C>A c.1027C>A c.(1027-1029)Ctg>Atg p.L343M COADREAD 16 68846069 68846069 + Missense_Mutation SNP C C A TCGA-A6-6648-01A-11D-1771-10 TCGA-A6-6648-10A-01D-1771-10 g.chr16:68846069C>A c.1040C>A c.(1039-1041)gCt>gAt p.A347D COADREAD 16 68846086 68846086 + Missense_Mutation SNP G G A TCGA-G4-6323-01A-11D-1719-10 TCGA-G4-6323-10A-01D-1720-10 g.chr16:68846086G>A c.1057G>A c.(1057-1059)Gag>Aag p.E353K COADREAD 16 68846087 68846087 + Missense_Mutation SNP A A G TCGA-A6-3809-01A-01W-0995-10 TCGA-A6-3809-11A-01W-0995-10 g.chr16:68846087A>G c.1058A>G c.(1057-1059)gAg>gGg p.E353G COADREAD 16 68846087 68846087 + Missense_Mutation SNP A A G TCGA-CA-5797-01A-01D-1650-10 TCGA-CA-5797-10A-01D-1650-10 g.chr16:68846087A>G c.1058A>G c.(1057-1059)gAg>gGg p.E353G COADREAD 16 68846087 68846087 + Missense_Mutation SNP A A G TCGA-CK-5912-01A-11D-1650-10 TCGA-CK-5912-10A-01D-1650-10 g.chr16:68846087A>G c.1058A>G c.(1057-1059)gAg>gGg p.E353G COADREAD 16 68846087 68846087 + Missense_Mutation SNP A A G TCGA-CK-5914-01A-11D-1650-10 TCGA-CK-5914-10A-01D-1650-10 g.chr16:68846087A>G c.1058A>G c.(1057-1059)gAg>gGg p.E353G COADREAD 16 68846087 68846087 + Missense_Mutation SNP A A G TCGA-CM-6678-01A-11D-1835-10 TCGA-CM-6678-10A-01D-1835-10 g.chr16:68846087A>G c.1058A>G c.(1057-1059)gAg>gGg p.E353G COADREAD 16 68846087 68846087 + Missense_Mutation SNP A A G TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr16:68846087A>G c.1058A>G c.(1057-1059)gAg>gGg p.E353G COADREAD 16 68846087 68846087 + Missense_Mutation SNP A A G TCGA-DM-A1HA-01A-11D-A152-10 TCGA-DM-A1HA-10A-01D-A152-10 g.chr16:68846087A>G c.1058A>G c.(1057-1059)gAg>gGg p.E353G COADREAD 16 68846088 68846088 + Silent SNP G G A TCGA-DM-A1D7-01A-11D-A152-10 TCGA-DM-A1D7-10A-01D-A152-10 g.chr16:68846088G>A c.1059G>A c.(1057-1059)gaG>gaA p.E353E COADREAD 16 68846098 68846098 + Missense_Mutation SNP A A G TCGA-AA-3502-01A-01D-1408-10 TCGA-AA-3502-11A-01D-1408-10 g.chr16:68846098A>G c.1069A>G c.(1069-1071)Aca>Gca p.T357A COADREAD 16 68846099 68846099 + Missense_Mutation SNP C C A TCGA-DM-A28E-01A-11D-A16V-10 TCGA-DM-A28E-10A-01D-A16V-10 g.chr16:68846099C>A c.1070C>A c.(1069-1071)aCa>aAa p.T357K COADREAD 16 68846118 68846119 + Frame_Shift_Del DEL CA CA - TCGA-CK-6747-01A-11D-1835-10 TCGA-CK-6747-10A-01D-1835-10 g.chr16:68846118_68846119delCA c.1089_1090delCA c.(1087-1092)atcacafs p.T364fs COADREAD 16 68846122 68846122 + Missense_Mutation SNP G G A TCGA-AA-3821-01A-01W-0995-10 TCGA-AA-3821-10A-01W-0995-10 g.chr16:68846122G>A c.1093G>A c.(1093-1095)Gtc>Atc p.V365I COADREAD 16 68846123 68846123 + Missense_Mutation SNP T T C TCGA-G4-6304-01A-11D-1924-10 TCGA-G4-6304-10A-01D-1924-10 g.chr16:68846123T>C c.1094T>C c.(1093-1095)gTc>gCc p.V365A COADREAD 16 68846134 68846134 + Missense_Mutation SNP A A G TCGA-AG-3731-01A-11D-1733-10 TCGA-AG-3731-11A-01D-1733-10 g.chr16:68846134A>G c.1105A>G c.(1105-1107)Aac>Gac p.N369D COADREAD 16 68846135 68846135 + Missense_Mutation SNP A A G TCGA-A6-6141-01A-11D-1771-10 TCGA-A6-6141-10A-01D-1771-10 g.chr16:68846135A>G c.1106A>G c.(1105-1107)aAc>aGc p.N369S COADREAD 16 68847235 68847235 + Missense_Mutation SNP A A G TCGA-CM-5349-01A-21D-1719-10 TCGA-CM-5349-10A-01D-1719-10 g.chr16:68847235A>G c.1157A>G c.(1156-1158)gAg>gGg p.E386G COADREAD 16 68847277 68847277 + Missense_Mutation SNP A A G TCGA-CK-4950-01A-01D-1719-10 TCGA-CK-4950-10A-01D-1719-10 g.chr16:68847277A>G c.1199A>G c.(1198-1200)gAt>gGt p.D400G COADREAD 16 68847283 68847283 + Missense_Mutation SNP A A G TCGA-D5-6536-01A-11D-1719-10 TCGA-D5-6536-10A-01D-1719-10 g.chr16:68847283A>G c.1205A>G c.(1204-1206)gAt>gGt p.D402G COADREAD 16 68847302 68847302 + Silent SNP G G A TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr16:68847302G>A c.1224G>A c.(1222-1224)gcG>gcA p.A408A COADREAD 16 68847361 68847361 + Missense_Mutation SNP A A G TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr16:68847361A>G c.1283A>G c.(1282-1284)aAt>aGt p.N428S COADREAD 16 68849464 68849464 + Missense_Mutation SNP T T C TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr16:68849464T>C c.1367T>C c.(1366-1368)gTg>gCg p.V456A COADREAD 16 68849464 68849464 + Missense_Mutation SNP T T C TCGA-DC-5337-01A-01D-1657-10 TCGA-DC-5337-10A-01D-1657-10 g.chr16:68849464T>C c.1367T>C c.(1366-1368)gTg>gCg p.V456A COADREAD 16 68849484 68849484 + Nonsense_Mutation SNP G G T TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr16:68849484G>T c.1387G>T c.(1387-1389)Gag>Tag p.E463* COADREAD 16 68849520 68849520 + Missense_Mutation SNP G G A TCGA-AH-6544-01A-11D-1826-10 TCGA-AH-6544-10A-01D-1826-10 g.chr16:68849520G>A c.1423G>A c.(1423-1425)Gtg>Atg p.V475M COADREAD 16 68849532 68849532 + Missense_Mutation SNP G G T TCGA-D5-6539-01A-11D-1719-10 TCGA-D5-6539-10A-01D-1719-10 g.chr16:68849532G>T c.1435G>T c.(1435-1437)Gat>Tat p.D479Y COADREAD 16 68849532 68849532 + Missense_Mutation SNP G G T TCGA-DM-A28F-01A-11D-A16V-10 TCGA-DM-A28F-10A-01D-A16V-10 g.chr16:68849532G>T c.1435G>T c.(1435-1437)Gat>Tat p.D479Y COADREAD 16 68849625 68849625 + Missense_Mutation SNP G G A TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr16:68849625G>A c.1528G>A c.(1528-1530)Gcc>Acc p.A510T COADREAD 16 68849661 68849661 + Splice_Site SNP A A G TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr16:68849661A>G c.1564A>G c.(1564-1566)Aca>Gca p.T522A COADREAD 16 68849661 68849661 + Splice_Site SNP A A G TCGA-G4-6321-01A-11D-1719-10 TCGA-G4-6321-10A-01D-1720-10 g.chr16:68849661A>G c.1564A>G c.(1564-1566)Aca>Gca p.T522A COADREAD 16 68849663 68849663 + Splice_Site SNP G G A TCGA-A6-5657-01A-01D-1650-10 TCGA-A6-5657-10A-01D-1650-10 g.chr16:68849663G>A c.e10+1 COADREAD 16 68849663 68849663 + Splice_Site SNP G G A TCGA-AA-3697-01A-01D-1719-10 TCGA-AA-3697-11A-01D-1719-10 g.chr16:68849663G>A c.e10+1 COADREAD 16 68849663 68849663 + Splice_Site SNP G G A TCGA-CM-5868-01A-01D-1650-10 TCGA-CM-5868-10A-01D-1650-10 g.chr16:68849663G>A c.e10+1 COADREAD 16 68849663 68849663 + Splice_Site SNP G G A TCGA-D5-6539-01A-11D-1719-10 TCGA-D5-6539-10A-01D-1719-10 g.chr16:68849663G>A c.e10+1 COADREAD 16 68853211 68853211 + Missense_Mutation SNP T T C TCGA-D5-6537-01A-11D-1719-10 TCGA-D5-6537-10A-01D-1719-10 g.chr16:68853211T>C c.1594T>C c.(1594-1596)Tgg>Cgg p.W532R COADREAD 16 68853211 68853211 + Missense_Mutation SNP T T C TCGA-DY-A1DG-01A-11D-A152-10 TCGA-DY-A1DG-10A-01D-A152-10 g.chr16:68853211T>C c.1594T>C c.(1594-1596)Tgg>Cgg p.W532R COADREAD 16 68853294 68853294 + Silent SNP C C T TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr16:68853294C>T c.1677C>T c.(1675-1677)agC>agT p.S559S COADREAD 16 68853328 68853328 + Splice_Site SNP G G A TCGA-CM-6161-01A-11D-1650-10 TCGA-CM-6161-10A-01D-1650-10 g.chr16:68853328G>A c.1711G>A c.(1711-1713)Ggt>Agt p.G571S COADREAD 16 68853330 68853330 + Splice_Site SNP T T A TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr16:68853330T>A c.e11+2 COADREAD 16 68853330 68853330 + Splice_Site SNP T T A TCGA-CM-5344-01A-21D-1719-10 TCGA-CM-5344-10A-01D-1719-10 g.chr16:68853330T>A c.e11+2 COADREAD 16 68853330 68853330 + Splice_Site SNP T T A TCGA-D5-6932-01A-11D-1924-10 TCGA-D5-6932-10A-01D-1924-10 g.chr16:68853330T>A c.e11+2 COADREAD 16 68853330 68853330 + Splice_Site SNP T T C TCGA-G4-6310-01A-11D-1719-10 TCGA-G4-6310-10A-01D-1720-10 g.chr16:68853330T>C c.e11+2 COADREAD 16 68855984 68855984 + Nonsense_Mutation SNP C C T TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr16:68855984C>T c.1792C>T c.(1792-1794)Cga>Tga p.R598* COADREAD 16 68855984 68855984 + Nonsense_Mutation SNP C C T TCGA-AY-6386-01A-21D-1719-10 TCGA-AY-6386-10A-01D-1719-10 g.chr16:68855984C>T c.1792C>T c.(1792-1794)Cga>Tga p.R598* COADREAD 16 68855987 68855987 + Missense_Mutation SNP A A G TCGA-D5-6535-01A-11D-1719-10 TCGA-D5-6535-10A-01D-1719-10 g.chr16:68855987A>G c.1795A>G c.(1795-1797)Act>Gct p.T599A COADREAD 16 68855987 68855987 + Missense_Mutation SNP A A G TCGA-D5-6539-01A-11D-1719-10 TCGA-D5-6539-10A-01D-1719-10 g.chr16:68855987A>G c.1795A>G c.(1795-1797)Act>Gct p.T599A COADREAD 16 68855988 68855988 + Missense_Mutation SNP C C T TCGA-DM-A282-01A-12D-A16V-10 TCGA-DM-A282-10A-01D-A16V-10 g.chr16:68855988C>T c.1796C>T c.(1795-1797)aCt>aTt p.T599I COADREAD 16 68855990 68855990 + Missense_Mutation SNP A A G TCGA-D5-6537-01A-11D-1719-10 TCGA-D5-6537-10A-01D-1719-10 g.chr16:68855990A>G c.1798A>G c.(1798-1800)Ata>Gta p.I600V COADREAD 16 68856041 68856041 + Missense_Mutation SNP G G A TCGA-CM-4752-01A-01D-1408-10 TCGA-CM-4752-10A-01D-1408-10 g.chr16:68856041G>A c.1849G>A c.(1849-1851)Gca>Aca p.A617T COADREAD 16 68856105 68856105 + Missense_Mutation SNP G G T TCGA-DM-A1D4-01A-21D-A152-10 TCGA-DM-A1D4-10A-01D-A152-10 g.chr16:68856105G>T c.1913G>T c.(1912-1914)tGg>tTg p.W638L COADREAD 16 68856105 68856105 + Nonsense_Mutation SNP G G A TCGA-AY-6386-01A-21D-1719-10 TCGA-AY-6386-10A-01D-1719-10 g.chr16:68856105G>A c.1913G>A c.(1912-1914)tGg>tAg p.W638* COADREAD 16 68857307 68857307 + Nonsense_Mutation SNP G G T TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr16:68857307G>T c.1942G>T c.(1942-1944)Gaa>Taa p.E648* COADREAD 16 68857418 68857418 + Missense_Mutation SNP G G A TCGA-AD-6964-01A-11D-1924-10 TCGA-AD-6964-10A-01D-1924-10 g.chr16:68857418G>A c.2053G>A c.(2053-2055)Gtg>Atg p.V685M COADREAD 16 68857497 68857497 + Missense_Mutation SNP T T A TCGA-F5-6465-01A-11D-1733-10 TCGA-F5-6465-10A-01D-1733-10 g.chr16:68857497T>A c.2132T>A c.(2131-2133)cTg>cAg p.L711Q COADREAD 16 68862096 68862097 + Silent DNP GC GC AT TCGA-AZ-6605-01A-11D-1835-10 TCGA-AZ-6605-11A-01D-1835-10 g.chr16:68862096_68862097GC>AT c.2184_2185GC>AT c.(2182-2187)ttGCtg>ttATtg p.728_729LL>LL COADREAD 16 68862164 68862164 + Missense_Mutation SNP A A G TCGA-A6-5662-01A-01D-1650-10 TCGA-A6-5662-10A-01D-1650-10 g.chr16:68862164A>G c.2252A>G c.(2251-2253)aAc>aGc p.N751S COADREAD 16 68862165 68862165 + Silent SNP C C T TCGA-D5-6923-01A-11D-1924-10 TCGA-D5-6923-10A-01D-1924-10 g.chr16:68862165C>T c.2253C>T c.(2251-2253)aaC>aaT p.N751N COADREAD 16 68863581 68863581 + Missense_Mutation SNP A A G TCGA-AZ-6599-01A-11D-1771-10 TCGA-AZ-6599-11A-01D-1771-10 g.chr16:68863581A>G c.2320A>G c.(2320-2322)Agg>Ggg p.R774G COADREAD 16 68867265 68867265 + Missense_Mutation SNP A A G TCGA-AA-3662-01A-01D-1719-10 TCGA-AA-3662-11A-01D-1719-10 g.chr16:68867265A>G c.2512A>G c.(2512-2514)Agc>Ggc p.S838G COADREAD 16 68867265 68867265 + Missense_Mutation SNP A A G TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr16:68867265A>G c.2512A>G c.(2512-2514)Agc>Ggc p.S838G COADREAD 16 68867267 68867267 + Silent SNP C C T TCGA-CK-4950-01A-01D-1719-10 TCGA-CK-4950-10A-01D-1719-10 g.chr16:68867267C>T c.2514C>T c.(2512-2514)agC>agT p.S838S COADREAD 16 68867289 68867289 + Missense_Mutation SNP A A G TCGA-G4-6306-01A-11D-1771-10 TCGA-G4-6306-10A-01D-1771-10 g.chr16:68867289A>G c.2536A>G c.(2536-2538)Agc>Ggc p.S846G COADREAD 16 68867291 68867291 + Silent SNP C C T TCGA-A6-5666-01A-01D-1650-10 TCGA-A6-5666-10A-01D-1650-10 g.chr16:68867291C>T c.2538C>T c.(2536-2538)agC>agT p.S846S COADREAD 16 68867304 68867304 + Missense_Mutation SNP T T C TCGA-CM-5348-01A-21D-1719-10 TCGA-CM-5348-10A-01D-1719-10 g.chr16:68867304T>C c.2551T>C c.(2551-2553)Tca>Cca p.S851P COADREAD 16 68867305 68867305 + Nonsense_Mutation SNP C C A TCGA-A6-6141-01A-11D-1771-10 TCGA-A6-6141-10A-01D-1771-10 g.chr16:68867305C>A c.2552C>A c.(2551-2553)tCa>tAa p.S851* DLBC 16 68855966 68855966 + Missense_Mutation SNP G G A TCGA-GR-7353-01A-11D-2210-10 TCGA-GR-7353-10A-01D-2210-10 g.chr16:68855966G>A c.1774G>A c.(1774-1776)Gcc>Acc p.A592T DLBC 16 68862165 68862165 + Silent SNP C C T TCGA-G8-6909-01A-11D-2210-10 TCGA-G8-6909-14A-01D-2210-10 g.chr16:68862165C>T c.2253C>T c.(2251-2253)aaC>aaT p.N751N ESCA 16 68849430 68849430 + Nonsense_Mutation SNP G G T TCGA-X8-AAAR-01A-11D-A403-09 TCGA-X8-AAAR-10A-01D-A403-09 g.chr16:68849430G>T c.1333G>T c.(1333-1335)Gag>Tag p.E445* GBM 16 68855965 68855965 + Silent SNP C C T TCGA-32-1982-01A-01D-1494-08 TCGA-32-1982-10A-01D-1494-08 g.chr16:68855965C>T c.1773C>T c.(1771-1773)aaC>aaT p.N591N GBMLGG 16 68844204 68844204 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:68844204G>T c.792G>T c.(790-792)caG>caT p.Q264H GBMLGG 16 68846137 68846137 + Missense_Mutation SNP G G A TCGA-HT-A617-01A-11D-A29Q-08 TCGA-HT-A617-10A-01D-A29Q-08 g.chr16:68846137G>A c.1108G>A c.(1108-1110)Gat>Aat p.D370N GBMLGG 16 68847221 68847221 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:68847221G>T c.1143G>T c.(1141-1143)aaG>aaT p.K381N GBMLGG 16 68847244 68847244 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:68847244C>T c.1166C>T c.(1165-1167)gCt>gTt p.A389V GBMLGG 16 68847374 68847374 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:68847374C>T c.1296C>T c.(1294-1296)aaC>aaT p.N432N GBMLGG 16 68855965 68855965 + Silent SNP C C T TCGA-32-1982-01A-01D-1494-08 TCGA-32-1982-10A-01D-1494-08 g.chr16:68855965C>T c.1773C>T c.(1771-1773)aaC>aaT p.N591N HNSC 16 68842735 68842735 + Missense_Mutation SNP G G A TCGA-CR-7370-01A-11D-2129-08 TCGA-CR-7370-10A-01D-2129-08 g.chr16:68842735G>A c.671G>A c.(670-672)cGc>cAc p.R224H HNSC 16 68847250 68847255 + In_Frame_Del DEL TCGTAA TCGTAA - TCGA-CN-6024-01A-11D-1683-08 TCGA-CN-6024-10A-01D-1683-08 g.chr16:68847250_68847255delTCGTAA c.1172_1177delTCGTAA c.(1171-1179)gtcgtaatc>gtc p.VI392del HNSC 16 68849489 68849489 + Silent SNP C C T TCGA-CV-5436-01A-01D-1512-08 TCGA-CV-5436-10A-01D-1870-08 g.chr16:68849489C>T c.1392C>T c.(1390-1392)gtC>gtT p.V464V HNSC 16 68853291 68853291 + Missense_Mutation SNP C C A TCGA-BA-4074-01A-01D-1434-08 TCGA-BA-4074-10A-01D-1434-08 g.chr16:68853291C>A c.1674C>A c.(1672-1674)aaC>aaA p.N558K HNSC 16 68853324 68853324 + Missense_Mutation SNP C C A TCGA-CV-6937-01A-11D-2012-08 TCGA-CV-6937-10A-01D-2013-08 g.chr16:68853324C>A c.1707C>A c.(1705-1707)gaC>gaA p.D569E HNSC 16 68857424 68857424 + Missense_Mutation SNP G G C TCGA-BB-A5HY-01A-11D-A28R-08 TCGA-BB-A5HY-10A-01D-A28U-08 g.chr16:68857424G>C c.2059G>C c.(2059-2061)Gac>Cac p.D687H HNSC 16 68867195 68867195 + Silent SNP T T C TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr16:68867195T>C c.2442T>C c.(2440-2442)aaT>aaC p.N814N KIPAN 16 68845698 68845698 + Missense_Mutation SNP A A G TCGA-B0-5692-01A-11D-1534-10 TCGA-B0-5692-11A-01D-1534-10 g.chr16:68845698A>G c.944A>G c.(943-945)aAt>aGt p.N315S KIPAN 16 68853183 68853183 + Splice_Site SNP A A C TCGA-B9-A69E-01A-11D-A31X-10 TCGA-B9-A69E-10A-01D-A31X-10 g.chr16:68853183A>C c.1566A>C c.(1564-1566)acA>acC p.T522T KIPAN 16 68862136 68862136 + Silent SNP C C T TCGA-BP-4977-01A-01D-1462-08 TCGA-BP-4977-11A-01D-1462-08 g.chr16:68862136C>T c.2224C>T c.(2224-2226)Ctg>Ttg p.L742L KIPAN 16 68867229 68867229 + Frame_Shift_Del DEL C C - TCGA-B9-A8YI-01A-21D-A36X-10 TCGA-B9-A8YI-10A-01D-A370-10 g.chr16:68867229delC c.2476delC c.(2476-2478)cctfs p.P826fs KIRC 16 68845698 68845698 + Missense_Mutation SNP A A G TCGA-B0-5692-01A-11D-1534-10 TCGA-B0-5692-11A-01D-1534-10 g.chr16:68845698A>G c.944A>G c.(943-945)aAt>aGt p.N315S KIRC 16 68862136 68862136 + Silent SNP C C T TCGA-BP-4977-01A-01D-1462-08 TCGA-BP-4977-11A-01D-1462-08 g.chr16:68862136C>T c.2224C>T c.(2224-2226)Ctg>Ttg p.L742L KIRP 16 68853183 68853183 + Splice_Site SNP A A C TCGA-B9-A69E-01A-11D-A31X-10 TCGA-B9-A69E-10A-01D-A31X-10 g.chr16:68853183A>C c.1566A>C c.(1564-1566)acA>acC p.T522T KIRP 16 68867229 68867229 + Frame_Shift_Del DEL C C - TCGA-B9-A8YI-01A-21D-A36X-10 TCGA-B9-A8YI-10A-01D-A370-10 g.chr16:68867229delC c.2476delC c.(2476-2478)cctfs p.P826fs LGG 16 68844204 68844204 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:68844204G>T c.792G>T c.(790-792)caG>caT p.Q264H LGG 16 68846137 68846137 + Missense_Mutation SNP G G A TCGA-HT-A617-01A-11D-A29Q-08 TCGA-HT-A617-10A-01D-A29Q-08 g.chr16:68846137G>A c.1108G>A c.(1108-1110)Gat>Aat p.D370N LGG 16 68847221 68847221 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:68847221G>T c.1143G>T c.(1141-1143)aaG>aaT p.K381N LGG 16 68847244 68847244 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:68847244C>T c.1166C>T c.(1165-1167)gCt>gTt p.A389V LGG 16 68847374 68847374 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:68847374C>T c.1296C>T c.(1294-1296)aaC>aaT p.N432N LIHC 16 68842624 68842624 + Missense_Mutation SNP A A G TCGA-DD-A4NK-01A-11D-A28X-10 TCGA-DD-A4NK-10A-01D-A28X-10 g.chr16:68842624A>G c.560A>G c.(559-561)aAg>aGg p.K187R LIHC 16 68849486 68849486 + Silent SNP G G A TCGA-RC-A7S9-01A-11D-A33Q-10 TCGA-RC-A7S9-10A-02D-A33Q-10 g.chr16:68849486G>A c.1389G>A c.(1387-1389)gaG>gaA p.E463E LIHC 16 68849586 68849586 + Nonsense_Mutation SNP G G T TCGA-DD-AADI-01A-11D-A40R-10 TCGA-DD-AADI-10A-01D-A40U-10 g.chr16:68849586G>T c.1489G>T c.(1489-1491)Gag>Tag p.E497* LIHC 16 68849632 68849632 + Missense_Mutation SNP A A T TCGA-DD-AADA-01A-11D-A40R-10 TCGA-DD-AADA-10A-01D-A40U-10 g.chr16:68849632A>T c.1535A>T c.(1534-1536)gAg>gTg p.E512V LIHC 16 68856096 68856096 + Missense_Mutation SNP G G T TCGA-DD-AAE3-01A-11D-A40R-10 TCGA-DD-AAE3-10A-01D-A40U-10 g.chr16:68856096G>T c.1904G>T c.(1903-1905)aGt>aTt p.S635I LIHC 16 68856129 68856129 + Splice_Site SNP G G A TCGA-CC-5260-01A-01D-A12Z-10 TCGA-CC-5260-10B-01D-A12Z-10 g.chr16:68856129G>A c.e12+1 LIHC 16 68856129 68856129 + Splice_Site SNP G G A TCGA-DD-A1EE-01A-11D-A12Z-10 TCGA-DD-A1EE-10A-01D-A12Z-10 g.chr16:68856129G>A c.e12+1 LIHC 16 68867249 68867250 + Frame_Shift_Ins INS - - T TCGA-2Y-A9H5-01A-11D-A382-10 TCGA-2Y-A9H5-10A-01D-A385-10 g.chr16:68867249_68867250insT c.2496_2497insT c.(2497-2499)tttfs p.F833fs LUAD 16 68835796 68835796 + Splice_Site SNP G G T TCGA-50-6590-01A-12D-1855-08 TCGA-50-6590-11A-01D-1855-08 g.chr16:68835796G>T c.387G>T c.(385-387)caG>caT p.Q129H LUAD 16 68846036 68846037 + Splice_Site DEL AG AG - TCGA-95-7567-01A-11D-2063-08 TCGA-95-7567-10A-01D-2063-08 g.chr16:68846036_68846037delAG c.e8-1 LUAD 16 68847300 68847300 + Missense_Mutation SNP G G C TCGA-55-A4DF-01A-11D-A24D-08 TCGA-55-A4DF-10A-01D-A24F-08 g.chr16:68847300G>C c.1222G>C c.(1222-1224)Gcg>Ccg p.A408P LUAD 16 68849475 68849475 + Missense_Mutation SNP G G T TCGA-44-2656-01A-02D-0969-08 TCGA-44-2656-10A-01D-0969-08 g.chr16:68849475G>T c.1378G>T c.(1378-1380)Gta>Tta p.V460L LUAD 16 68857305 68857305 + Missense_Mutation SNP A A T TCGA-55-8614-01A-11D-2393-08 TCGA-55-8614-10A-01D-2393-08 g.chr16:68857305A>T c.1940A>T c.(1939-1941)cAa>cTa p.Q647L LUAD 16 68862085 68862085 + Silent SNP C C T TCGA-78-7152-01A-11D-2036-08 TCGA-78-7152-10A-01D-2036-08 g.chr16:68862085C>T c.2173C>T c.(2173-2175)Ctg>Ttg p.L725L LUAD 16 68862125 68862125 + Missense_Mutation SNP A A G TCGA-05-5428-01A-01D-1625-08 TCGA-05-5428-10A-01D-1625-08 g.chr16:68862125A>G c.2213A>G c.(2212-2214)aAa>aGa p.K738R LUSC 16 68835620 68835620 + Missense_Mutation SNP C C T TCGA-22-1016-01A-01D-1521-08 TCGA-22-1016-11A-01D-1521-08 g.chr16:68835620C>T c.211C>T c.(211-213)Ctc>Ttc p.L71F LUSC 16 68844241 68844241 + Missense_Mutation SNP C C T TCGA-21-5787-01A-01D-1632-08 TCGA-21-5787-10A-01D-1632-08 g.chr16:68844241C>T c.829C>T c.(829-831)Cca>Tca p.P277S LUSC 16 68849430 68849430 + Missense_Mutation SNP G G C TCGA-66-2759-01A-01D-1522-08 TCGA-66-2759-11A-01D-1522-08 g.chr16:68849430G>C c.1333G>C c.(1333-1335)Gag>Cag p.E445Q OV 16 68842726 68842726 + Missense_Mutation SNP A A T TCGA-42-2590-01A-01D-1526-09 TCGA-42-2590-10A-01D-1526-09 g.chr16:68842726A>T c.662A>T c.(661-663)gAt>gTt p.D221V OV 16 68845700 68845700 + Missense_Mutation SNP A A G TCGA-04-1337-01A-01W-0484-10 TCGA-04-1337-11A-01W-0485-10 g.chr16:68845700A>G c.946A>G c.(946-948)Atg>Gtg p.M316V PAAD 16 68863587 68863587 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr16:68863587C>A c.2326C>A c.(2326-2328)Ctg>Atg p.L776M PRAD 16 68844157 68844157 + Missense_Mutation SNP T T G TCGA-EJ-7782-01A-11D-2114-08 TCGA-EJ-7782-10A-01D-2114-08 g.chr16:68844157T>G c.745T>G c.(745-747)Ttg>Gtg p.L249V PRAD 16 68846165 68846165 + Splice_Site SNP C C T TCGA-G9-6365-01A-11D-1786-08 TCGA-G9-6365-10A-01D-1786-08 g.chr16:68846165C>T c.1136C>T c.(1135-1137)aCg>aTg p.T379M PRAD 16 68847380 68847380 + Silent SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr16:68847380C>T c.1302C>T c.(1300-1302)ggC>ggT p.G434G PRAD 16 68855984 68855984 + Missense_Mutation SNP C C G TCGA-KK-A6E8-01A-11D-A31L-08 TCGA-KK-A6E8-11A-11D-A31J-08 g.chr16:68855984C>G c.1792C>G c.(1792-1794)Cga>Gga p.R598G PRAD 16 68856088 68856088 + Frame_Shift_Del DEL C C - TCGA-KK-A59V-01A-11D-A29Q-08 TCGA-KK-A59V-11A-11D-A29Q-08 g.chr16:68856088delC c.1896delC c.(1894-1896)cacfs p.H632fs READ 16 68772219 68772219 + Missense_Mutation SNP A A G TCGA-AG-3732-01A-11D-1657-10 TCGA-AG-3732-11A-01D-1657-10 g.chr16:68772219A>G c.68A>G c.(67-69)cAg>cGg p.Q23R READ 16 68835630 68835630 + Missense_Mutation SNP G G A TCGA-G5-6235-01A-11D-1733-10 TCGA-G5-6235-10A-01D-1733-10 g.chr16:68835630G>A c.221G>A c.(220-222)cGa>cAa p.R74Q READ 16 68835727 68835727 + Silent SNP C C T TCGA-F5-6811-01A-11D-1826-10 TCGA-F5-6811-10A-01D-1826-10 g.chr16:68835727C>T c.318C>T c.(316-318)acC>acT p.T106T READ 16 68844110 68844110 + Missense_Mutation SNP A A G TCGA-EF-5830-01A-01D-1657-10 TCGA-EF-5830-10A-01D-1657-10 g.chr16:68844110A>G c.698A>G c.(697-699)cAc>cGc p.H233R READ 16 68844147 68844147 + Silent SNP A A G TCGA-AF-2687-01A-02D-1733-10 TCGA-AF-2687-10A-01D-1733-10 g.chr16:68844147A>G c.735A>G c.(733-735)ccA>ccG p.P245P READ 16 68844172 68844172 + Missense_Mutation SNP G G A TCGA-AF-2687-01A-02D-1733-10 TCGA-AF-2687-10A-01D-1733-10 g.chr16:68844172G>A c.760G>A c.(760-762)Gat>Aat p.D254N READ 16 68845617 68845617 + Missense_Mutation SNP A A G TCGA-AF-6136-01A-11D-1826-10 TCGA-AF-6136-10A-01D-1826-10 g.chr16:68845617A>G c.863A>G c.(862-864)gAc>gGc p.D288G READ 16 68846036 68846036 + Splice_Site SNP A A G TCGA-AH-6643-01A-11D-1826-10 TCGA-AH-6643-11A-01D-1826-10 g.chr16:68846036A>G c.e8-1 READ 16 68846134 68846134 + Missense_Mutation SNP A A G TCGA-AG-3731-01A-11D-1733-10 TCGA-AG-3731-11A-01D-1733-10 g.chr16:68846134A>G c.1105A>G c.(1105-1107)Aac>Gac p.N369D READ 16 68849464 68849464 + Missense_Mutation SNP T T C TCGA-DC-5337-01A-01D-1657-10 TCGA-DC-5337-10A-01D-1657-10 g.chr16:68849464T>C c.1367T>C c.(1366-1368)gTg>gCg p.V456A READ 16 68849520 68849520 + Missense_Mutation SNP G G A TCGA-AH-6544-01A-11D-1826-10 TCGA-AH-6544-10A-01D-1826-10 g.chr16:68849520G>A c.1423G>A c.(1423-1425)Gtg>Atg p.V475M READ 16 68853211 68853211 + Missense_Mutation SNP T T C TCGA-DY-A1DG-01A-11D-A152-10 TCGA-DY-A1DG-10A-01D-A152-10 g.chr16:68853211T>C c.1594T>C c.(1594-1596)Tgg>Cgg p.W532R READ 16 68857307 68857307 + Nonsense_Mutation SNP G G T TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr16:68857307G>T c.1942G>T c.(1942-1944)Gaa>Taa p.E648* READ 16 68857497 68857497 + Missense_Mutation SNP T T A TCGA-F5-6465-01A-11D-1733-10 TCGA-F5-6465-10A-01D-1733-10 g.chr16:68857497T>A c.2132T>A c.(2131-2133)cTg>cAg p.L711Q SKCM 16 68835619 68835619 + Silent SNP C C T TCGA-EE-A2GR-06A-11D-A197-08 TCGA-EE-A2GR-10A-01D-A199-08 g.chr16:68835619C>T c.210C>T c.(208-210)tcC>tcT p.S70S SKCM 16 68835626 68835627 + Frame_Shift_Ins INS - - C TCGA-OD-A75X-06A-12D-A32N-08 TCGA-OD-A75X-10A-01D-A32N-08 g.chr16:68835626_68835627insC c.217_218insC c.(217-219)accfs p.T73fs SKCM 16 68842665 68842665 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr16:68842665C>T c.601C>T c.(601-603)Cct>Tct p.P201S SKCM 16 68844210 68844210 + Silent SNP C C T TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr16:68844210C>T c.798C>T c.(796-798)gtC>gtT p.V266V SKCM 16 68847364 68847364 + Missense_Mutation SNP C C T TCGA-FS-A1ZK-06A-11D-A197-08 TCGA-FS-A1ZK-10A-01D-A199-08 g.chr16:68847364C>T c.1286C>T c.(1285-1287)cCa>cTa p.P429L SKCM 16 68856025 68856025 + Silent SNP C C T TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr16:68856025C>T c.1833C>T c.(1831-1833)gtC>gtT p.V611V SKCM 16 68857521 68857521 + Missense_Mutation SNP C C T TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr16:68857521C>T c.2156C>T c.(2155-2157)gCt>gTt p.A719V SKCM 16 68862142 68862142 + Missense_Mutation SNP C C T TCGA-EE-A2A6-06A-11D-A197-08 TCGA-EE-A2A6-10A-01D-A199-08 g.chr16:68862142C>T c.2230C>T c.(2230-2232)Cca>Tca p.P744S SKCM 16 68867355 68867355 + Missense_Mutation SNP C C T TCGA-RP-A694-06A-11D-A30X-08 TCGA-RP-A694-10A-01D-A30X-08 g.chr16:68867355C>T c.2602C>T c.(2602-2604)Cgc>Tgc p.R868C ACC 19 3525978 3525978 + Missense_Mutation SNP T T G TCGA-OR-A5KP-01A-11D-A30A-10 TCGA-OR-A5KP-10A-01D-A30A-10 g.chr19:3525978T>G c.182T>G c.(181-183)tTc>tGc p.F61C ACC 19 3527019 3527019 + Silent SNP C C T TCGA-PK-A5H8-01A-11D-A29I-10 TCGA-PK-A5H8-10A-01D-A29L-10 g.chr19:3527019C>T c.429C>T c.(427-429)aaC>aaT p.N143N ACC 19 3532525 3532525 + Frame_Shift_Del DEL G G - TCGA-OR-A5J5-01A-11D-A29I-10 TCGA-OR-A5J5-10A-01D-A29L-10 g.chr19:3532525delG c.1119delG c.(1117-1119)tcgfs p.S373fs BLCA 19 3526167 3526167 + Nonsense_Mutation SNP C C G TCGA-LT-A5Z6-01A-11D-A289-08 TCGA-LT-A5Z6-10A-01D-A289-08 g.chr19:3526167C>G c.245C>G c.(244-246)tCa>tGa p.S82* BLCA 19 3527000 3527000 + Missense_Mutation SNP C C G TCGA-UY-A78O-01A-12D-A339-08 TCGA-UY-A78O-10A-01D-A339-08 g.chr19:3527000C>G c.410C>G c.(409-411)tCc>tGc p.S137C BLCA 19 3527044 3527044 + Missense_Mutation SNP C C A TCGA-DK-A3WW-01A-22D-A23M-08 TCGA-DK-A3WW-10A-01D-A23K-08 g.chr19:3527044C>A c.454C>A c.(454-456)Ccc>Acc p.P152T BLCA 19 3531970 3531970 + Silent SNP G G A TCGA-XF-AAN3-01A-11D-A42E-08 TCGA-XF-AAN3-10A-01D-A42H-08 g.chr19:3531970G>A c.885G>A c.(883-885)caG>caA p.Q295Q BLCA 19 3532434 3532434 + Missense_Mutation SNP C C T TCGA-SY-A9G5-01A-11D-A38G-08 TCGA-SY-A9G5-10A-01D-A38J-08 g.chr19:3532434C>T c.1028C>T c.(1027-1029)tCg>tTg p.S343L BLCA 19 3534500 3534500 + Missense_Mutation SNP C C T TCGA-FD-A3N5-01A-11D-A21A-08 TCGA-FD-A3N5-10A-01D-A21A-08 g.chr19:3534500C>T c.1429C>T c.(1429-1431)Cgt>Tgt p.R477C CESC 19 3526310 3526310 + Missense_Mutation SNP G G A TCGA-EK-A2RN-01A-12D-A20U-09 TCGA-EK-A2RN-10A-01D-A20U-09 g.chr19:3526310G>A c.313G>A c.(313-315)Gag>Aag p.E105K CESC 19 3532042 3532042 + Silent SNP C C G TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr19:3532042C>G c.957C>G c.(955-957)ctC>ctG p.L319L CESC 19 3532541 3532541 + Missense_Mutation SNP G G C TCGA-DG-A2KL-01A-11D-A17W-09 TCGA-DG-A2KL-10A-01D-A17W-09 g.chr19:3532541G>C c.1135G>C c.(1135-1137)Gac>Cac p.D379H COAD 19 3527652 3527652 + Missense_Mutation SNP G G A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr19:3527652G>A c.494G>A c.(493-495)cGg>cAg p.R165Q COAD 19 3530853 3530853 + Missense_Mutation SNP C C T TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr19:3530853C>T c.718C>T c.(718-720)Cgg>Tgg p.R240W COAD 19 3531748 3531748 + Missense_Mutation SNP G G A TCGA-G4-6315-01A-11D-1719-10 TCGA-G4-6315-10A-01D-1720-10 g.chr19:3531748G>A c.757G>A c.(757-759)Gtg>Atg p.V253M COADREAD 19 3527642 3527642 + Missense_Mutation SNP C C T TCGA-DY-A1H8-01A-21D-A152-10 TCGA-DY-A1H8-10A-01D-A152-10 g.chr19:3527642C>T c.484C>T c.(484-486)Cgg>Tgg p.R162W COADREAD 19 3527652 3527652 + Missense_Mutation SNP G G A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr19:3527652G>A c.494G>A c.(493-495)cGg>cAg p.R165Q COADREAD 19 3530853 3530853 + Missense_Mutation SNP C C T TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr19:3530853C>T c.718C>T c.(718-720)Cgg>Tgg p.R240W COADREAD 19 3531748 3531748 + Missense_Mutation SNP G G A TCGA-G4-6315-01A-11D-1719-10 TCGA-G4-6315-10A-01D-1720-10 g.chr19:3531748G>A c.757G>A c.(757-759)Gtg>Atg p.V253M DLBC 19 3532490 3532490 + Missense_Mutation SNP G G A TCGA-FF-8046-01A-11D-2210-10 TCGA-FF-8046-10A-01D-2210-10 g.chr19:3532490G>A c.1084G>A c.(1084-1086)Gcc>Acc p.A362T ESCA 19 3525874 3525874 + Missense_Mutation SNP G G T TCGA-L5-A8NL-01A-12D-A37C-09 TCGA-L5-A8NL-11A-12D-A37F-09 g.chr19:3525874G>T c.78G>T c.(76-78)gaG>gaT p.E26D ESCA 19 3525967 3525967 + Nonsense_Mutation SNP G G A TCGA-L5-A8NQ-01A-11D-A36J-09 TCGA-L5-A8NQ-11A-11D-A36M-09 g.chr19:3525967G>A c.171G>A c.(169-171)tgG>tgA p.W57* ESCA 19 3530789 3530789 + Splice_Site SNP G G T TCGA-JY-A6FG-01A-11D-A33E-09 TCGA-JY-A6FG-10A-01D-A33H-09 g.chr19:3530789G>T c.e7-1 ESCA 19 3534441 3534441 + Missense_Mutation SNP C C T TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr19:3534441C>T c.1370C>T c.(1369-1371)gCc>gTc p.A457V GBM 19 3531983 3531983 + Missense_Mutation SNP A A C TCGA-06-1804-01A-01D-1696-08 TCGA-06-1804-10A-01D-1696-08 g.chr19:3531983A>C c.898A>C c.(898-900)Acc>Ccc p.T300P GBMLGG 19 3527008 3527008 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr19:3527008G>A c.418G>A c.(418-420)Gat>Aat p.D140N GBMLGG 19 3527700 3527700 + Missense_Mutation SNP C C T TCGA-QH-A6CU-01A-11D-A31L-08 TCGA-QH-A6CU-10A-01D-A31J-08 g.chr19:3527700C>T c.542C>T c.(541-543)gCg>gTg p.A181V GBMLGG 19 3531983 3531983 + Missense_Mutation SNP A A C TCGA-06-1804-01A-01D-1696-08 TCGA-06-1804-10A-01D-1696-08 g.chr19:3531983A>C c.898A>C c.(898-900)Acc>Ccc p.T300P GBMLGG 19 3532532 3532532 + Missense_Mutation SNP G G C TCGA-E1-5303-01A-01D-1468-08 TCGA-E1-5303-10A-01D-1468-08 g.chr19:3532532G>C c.1126G>C c.(1126-1128)Ggc>Cgc p.G376R HNSC 19 3526180 3526181 + Splice_Site INS - - G TCGA-D6-8568-01A-11D-2394-08 TCGA-D6-8568-10A-01D-2394-08 g.chr19:3526180_3526181insG c.258_259insG c.(259-261)gac>Ggac p.D87fs HNSC 19 3526259 3526259 + Missense_Mutation SNP G G A TCGA-CV-7180-01A-11D-2012-08 TCGA-CV-7180-10A-01D-2013-08 g.chr19:3526259G>A c.262G>A c.(262-264)Ggc>Agc p.G88S HNSC 19 3526992 3526992 + Silent SNP C C T TCGA-CV-A45U-01A-12D-A24D-08 TCGA-CV-A45U-10A-01D-A24F-08 g.chr19:3526992C>T c.402C>T c.(400-402)acC>acT p.T134T HNSC 19 3527705 3527705 + Missense_Mutation SNP G G A TCGA-CR-7371-01A-11D-2012-08 TCGA-CR-7371-10A-01D-2013-08 g.chr19:3527705G>A c.547G>A c.(547-549)Gag>Aag p.E183K HNSC 19 3534431 3534431 + Missense_Mutation SNP G G A TCGA-UF-A7JT-01A-11D-A34J-08 TCGA-UF-A7JT-10A-01D-A34M-08 g.chr19:3534431G>A c.1360G>A c.(1360-1362)Gat>Aat p.D454N KIPAN 19 3523035 3523035 + Missense_Mutation SNP G G C TCGA-CW-6093-01A-11D-1669-08 TCGA-CW-6093-11A-01D-1669-08 g.chr19:3523035G>C c.48G>C c.(46-48)caG>caC p.Q16H KIPAN 19 3527659 3527659 + Silent SNP C C A TCGA-B9-5156-01A-01D-1589-08 TCGA-B9-5156-10A-01D-1589-08 g.chr19:3527659C>A c.501C>A c.(499-501)ccC>ccA p.P167P KIPAN 19 3527661 3527661 + Missense_Mutation SNP C C G TCGA-P4-AAVL-01A-11D-A42J-10 TCGA-P4-AAVL-11A-11D-A42M-10 g.chr19:3527661C>G c.503C>G c.(502-504)aCc>aGc p.T168S KIPAN 19 3531748 3531748 + Missense_Mutation SNP G G A TCGA-CJ-4895-01A-01D-1373-10 TCGA-CJ-4895-11A-01D-1373-10 g.chr19:3531748G>A c.757G>A c.(757-759)Gtg>Atg p.V253M KIPAN 19 3532608 3532608 + Missense_Mutation SNP A A G TCGA-BP-4774-01A-01D-1366-10 TCGA-BP-4774-11A-01D-1367-10 g.chr19:3532608A>G c.1202A>G c.(1201-1203)cAa>cGa p.Q401R KIPAN 19 3533330 3533330 + Silent SNP C C A TCGA-BP-4976-01A-01D-1462-08 TCGA-BP-4976-11A-01D-1462-08 g.chr19:3533330C>A c.1281C>A c.(1279-1281)gtC>gtA p.V427V KIPAN 19 3533336 3533336 + Silent SNP G G A TCGA-B0-4706-01A-01D-1501-10 TCGA-B0-4706-11A-02D-1501-10 g.chr19:3533336G>A c.1287G>A c.(1285-1287)aaG>aaA p.K429K KIRC 19 3523035 3523035 + Missense_Mutation SNP G G C TCGA-CW-6093-01A-11D-1669-08 TCGA-CW-6093-11A-01D-1669-08 g.chr19:3523035G>C c.48G>C c.(46-48)caG>caC p.Q16H KIRC 19 3531748 3531748 + Missense_Mutation SNP G G A TCGA-CJ-4895-01A-01D-1373-10 TCGA-CJ-4895-11A-01D-1373-10 g.chr19:3531748G>A c.757G>A c.(757-759)Gtg>Atg p.V253M KIRC 19 3532608 3532608 + Missense_Mutation SNP A A G TCGA-BP-4774-01A-01D-1366-10 TCGA-BP-4774-11A-01D-1367-10 g.chr19:3532608A>G c.1202A>G c.(1201-1203)cAa>cGa p.Q401R KIRC 19 3533330 3533330 + Silent SNP C C A TCGA-BP-4976-01A-01D-1462-08 TCGA-BP-4976-11A-01D-1462-08 g.chr19:3533330C>A c.1281C>A c.(1279-1281)gtC>gtA p.V427V KIRC 19 3533336 3533336 + Silent SNP G G A TCGA-B0-4706-01A-01D-1501-10 TCGA-B0-4706-11A-02D-1501-10 g.chr19:3533336G>A c.1287G>A c.(1285-1287)aaG>aaA p.K429K KIRP 19 3527659 3527659 + Silent SNP C C A TCGA-B9-5156-01A-01D-1589-08 TCGA-B9-5156-10A-01D-1589-08 g.chr19:3527659C>A c.501C>A c.(499-501)ccC>ccA p.P167P KIRP 19 3527661 3527661 + Missense_Mutation SNP C C G TCGA-P4-AAVL-01A-11D-A42J-10 TCGA-P4-AAVL-11A-11D-A42M-10 g.chr19:3527661C>G c.503C>G c.(502-504)aCc>aGc p.T168S LGG 19 3527008 3527008 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr19:3527008G>A c.418G>A c.(418-420)Gat>Aat p.D140N LGG 19 3527700 3527700 + Missense_Mutation SNP C C T TCGA-QH-A6CU-01A-11D-A31L-08 TCGA-QH-A6CU-10A-01D-A31J-08 g.chr19:3527700C>T c.542C>T c.(541-543)gCg>gTg p.A181V LGG 19 3532532 3532532 + Missense_Mutation SNP G G C TCGA-E1-5303-01A-01D-1468-08 TCGA-E1-5303-10A-01D-1468-08 g.chr19:3532532G>C c.1126G>C c.(1126-1128)Ggc>Cgc p.G376R LIHC 19 3522996 3522996 + Silent SNP G G A TCGA-NI-A4U2-01A-11D-A28X-10 TCGA-NI-A4U2-10A-01D-A28X-10 g.chr19:3522996G>A c.9G>A c.(7-9)caG>caA p.Q3Q LIHC 19 3527733 3527733 + Missense_Mutation SNP T T G TCGA-DD-A116-01A-11D-A12Z-10 TCGA-DD-A116-10A-01D-A12Z-10 g.chr19:3527733T>G c.575T>G c.(574-576)cTg>cGg p.L192R LIHC 19 3530851 3530851 + Missense_Mutation SNP A A G TCGA-FV-A2QR-01A-11D-A20W-10 TCGA-FV-A2QR-11A-11D-A20W-10 g.chr19:3530851A>G c.716A>G c.(715-717)gAg>gGg p.E239G LIHC 19 3531769 3531769 + Missense_Mutation SNP G G A TCGA-DD-AACE-01A-11D-A40R-10 TCGA-DD-AACE-10A-01D-A40U-10 g.chr19:3531769G>A c.778G>A c.(778-780)Gca>Aca p.A260T LIHC 19 3531921 3531921 + Nonsense_Mutation SNP G G A TCGA-DD-AAVV-01A-11D-A40R-10 TCGA-DD-AAVV-10A-01D-A40U-10 g.chr19:3531921G>A c.836G>A c.(835-837)tGg>tAg p.W279* LIHC 19 3532454 3532454 + Nonsense_Mutation SNP C C T TCGA-G3-A7M8-01A-11D-A33Q-10 TCGA-G3-A7M8-10A-01D-A33Q-10 g.chr19:3532454C>T c.1048C>T c.(1048-1050)Cag>Tag p.Q350* LIHC 19 3534791 3534791 + Splice_Site SNP A A G TCGA-DD-AAEE-01A-11D-A40R-10 TCGA-DD-AAEE-10A-01D-A40U-10 g.chr19:3534791A>G c.e13-1 LUAD 19 3525945 3525945 + Missense_Mutation SNP C C A TCGA-73-4662-01A-01D-1265-08 TCGA-73-4662-11A-01D-1265-08 g.chr19:3525945C>A c.149C>A c.(148-150)cCc>cAc p.P50H LUAD 19 3527758 3527758 + Silent SNP G G T TCGA-55-7907-01A-11D-2167-08 TCGA-55-7907-10A-01D-2167-08 g.chr19:3527758G>T c.600G>T c.(598-600)gtG>gtT p.V200V LUAD 19 3532599 3532599 + Missense_Mutation SNP C C T TCGA-95-7039-01A-11D-1945-08 TCGA-95-7039-10A-01D-1946-08 g.chr19:3532599C>T c.1193C>T c.(1192-1194)aCg>aTg p.T398M LUAD 19 3533341 3533341 + Missense_Mutation SNP C C T TCGA-50-5942-01A-21D-1753-08 TCGA-50-5942-10A-01D-1753-08 g.chr19:3533341C>T c.1292C>T c.(1291-1293)cCc>cTc p.P431L PRAD 19 3525878 3525878 + Missense_Mutation SNP C C T TCGA-KK-A59V-01A-11D-A29Q-08 TCGA-KK-A59V-11A-11D-A29Q-08 g.chr19:3525878C>T c.82C>T c.(82-84)Cgg>Tgg p.R28W PRAD 19 3526341 3526341 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr19:3526341G>A c.344G>A c.(343-345)cGc>cAc p.R115H PRAD 19 3527681 3527681 + Missense_Mutation SNP C C G TCGA-EJ-7786-01A-11D-2114-08 TCGA-EJ-7786-10A-01D-2114-08 g.chr19:3527681C>G c.523C>G c.(523-525)Ccc>Gcc p.P175A PRAD 19 3527745 3527745 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr19:3527745C>T c.587C>T c.(586-588)tCg>tTg p.S196L PRAD 19 3532474 3532474 + Silent SNP G G A TCGA-KK-A59V-01A-11D-A29Q-08 TCGA-KK-A59V-11A-11D-A29Q-08 g.chr19:3532474G>A c.1068G>A c.(1066-1068)gcG>gcA p.A356A READ 19 3527642 3527642 + Missense_Mutation SNP C C T TCGA-DY-A1H8-01A-21D-A152-10 TCGA-DY-A1H8-10A-01D-A152-10 g.chr19:3527642C>T c.484C>T c.(484-486)Cgg>Tgg p.R162W SARC 19 3526982 3526982 + Missense_Mutation SNP C C T TCGA-DX-A8BP-01A-11D-A37C-09 TCGA-DX-A8BP-10A-01D-A37F-09 g.chr19:3526982C>T c.392C>T c.(391-393)tCc>tTc p.S131F SARC 19 3534432 3534432 + Missense_Mutation SNP A A T TCGA-FX-A3TO-01A-11D-A228-09 TCGA-FX-A3TO-10A-01D-A22A-09 g.chr19:3534432A>T c.1361A>T c.(1360-1362)gAt>gTt p.D454V SKCM 19 3523026 3523026 + Silent SNP C C T TCGA-EE-A20H-06A-11D-A197-08 TCGA-EE-A20H-10A-01D-A199-08 g.chr19:3523026C>T c.39C>T c.(37-39)atC>atT p.I13I SKCM 19 3525944 3525944 + Missense_Mutation SNP C C T TCGA-ER-A19E-06A-11D-A197-08 TCGA-ER-A19E-10A-01D-A199-08 g.chr19:3525944C>T c.148C>T c.(148-150)Ccc>Tcc p.P50S SKCM 19 3526174 3526174 + Missense_Mutation SNP C C A TCGA-D9-A1JX-06A-11D-A19A-08 TCGA-D9-A1JX-10A-01D-A19A-08 g.chr19:3526174C>A c.252C>A c.(250-252)aaC>aaA p.N84K SKCM 19 3526983 3526983 + Silent SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr19:3526983C>T c.393C>T c.(391-393)tcC>tcT p.S131S SKCM 19 3527037 3527037 + Silent SNP C C T TCGA-D3-A51T-06A-11D-A25O-08 TCGA-D3-A51T-10A-01D-A25O-08 g.chr19:3527037C>T c.447C>T c.(445-447)tcC>tcT p.S149S SKCM 19 3527037 3527037 + Silent SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr19:3527037C>T c.447C>T c.(445-447)tcC>tcT p.S149S SKCM 19 3527673 3527673 + Missense_Mutation SNP C C T TCGA-EE-A20C-06A-11D-A196-08 TCGA-EE-A20C-10A-01D-A198-08 g.chr19:3527673C>T c.515C>T c.(514-516)tCc>tTc p.S172F SKCM 19 3527686 3527686 + Silent SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr19:3527686C>T c.528C>T c.(526-528)ttC>ttT p.F176F SKCM 19 3527703 3527703 + Missense_Mutation SNP C C T TCGA-GN-A26A-06A-11D-A19A-08 TCGA-GN-A26A-10A-01D-A19A-08 g.chr19:3527703C>T c.545C>T c.(544-546)cCc>cTc p.P182L SKCM 19 3527704 3527704 + Silent SNP C C T TCGA-GN-A26A-06A-11D-A19A-08 TCGA-GN-A26A-10A-01D-A19A-08 g.chr19:3527704C>T c.546C>T c.(544-546)ccC>ccT p.P182P SKCM 19 3527745 3527745 + Missense_Mutation SNP C C T TCGA-D3-A3ML-06A-11D-A21A-08 TCGA-D3-A3ML-10A-01D-A21A-08 g.chr19:3527745C>T c.587C>T c.(586-588)tCg>tTg p.S196L SKCM 19 3527749 3527749 + Silent SNP C C A TCGA-DA-A1I7-06A-22D-A197-08 TCGA-DA-A1I7-10A-01D-A199-08 g.chr19:3527749C>A c.591C>A c.(589-591)tcC>tcA p.S197S SKCM 19 3527805 3527805 + Missense_Mutation SNP C C T TCGA-GN-A262-06A-11D-A196-08 TCGA-GN-A262-10A-01D-A198-08 g.chr19:3527805C>T c.647C>T c.(646-648)aCc>aTc p.T216I SKCM 19 3527806 3527806 + Silent SNP C C T TCGA-GN-A262-06A-11D-A196-08 TCGA-GN-A262-10A-01D-A198-08 g.chr19:3527806C>T c.648C>T c.(646-648)acC>acT p.T216T SKCM 19 3532524 3532525 + Frame_Shift_Ins INS - - G TCGA-FS-A4FD-06A-11D-A25O-08 TCGA-FS-A4FD-10B-01D-A25O-08 g.chr19:3532524_3532525insG c.1118_1119insG c.(1117-1122)tcggggfs p.SG373fs SKCM 19 3533377 3533377 + Missense_Mutation SNP C C T TCGA-EE-A2GO-06A-11D-A196-08 TCGA-EE-A2GO-10A-01D-A198-08 g.chr19:3533377C>T c.1328C>T c.(1327-1329)tCc>tTc p.S443F

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-US 19 3527044 3527044 single base substitution C A exon_variant BLCA-US 19 3527044 3527044 single base substitution C A intron_variant BLCA-US 19 3527044 3527044 single base substitution C A missense_variant P152T 454C>A BLCA-US 19 3534500 3534500 single base substitution C T 3_prime_UTR_variant BLCA-US 19 3534500 3534500 single base substitution C T downstream_gene_variant BLCA-US 19 3534500 3534500 single base substitution C T exon_variant BLCA-US 19 3534500 3534500 single base substitution C T missense_variant R388C 1162C>T BLCA-US 19 3534500 3534500 single base substitution C T missense_variant R477C 1429C>T BRCA-EU 19 3502393 3502393 single base substitution G C upstream_gene_variant BRCA-EU 19 3502486 3502486 single base substitution G A upstream_gene_variant BRCA-EU 19 3502921 3502921 single base substitution C G upstream_gene_variant BRCA-EU 19 3503236 3503236 single base substitution C T upstream_gene_variant BRCA-EU 19 3504385 3504385 single base substitution C T upstream_gene_variant BRCA-EU 19 3505229 3505229 single base substitution G A upstream_gene_variant BRCA-EU 19 3508551 3508551 single base substitution G T intron_variant BRCA-EU 19 3508806 3508808 deletion of <=200bp TGC - intron_variant BRCA-EU 19 3508885 3508885 single base substitution C T intron_variant BRCA-EU 19 3513055 3513055 single base substitution G T intron_variant BRCA-EU 19 3515195 3515195 single base substitution C A intron_variant BRCA-EU 19 3516831 3516831 single base substitution G A intron_variant BRCA-EU 19 3517148 3517148 single base substitution G A intron_variant BRCA-EU 19 3519870 3519870 single base substitution C T intron_variant BRCA-EU 19 3519870 3519870 single base substitution C T upstream_gene_variant BRCA-EU 19 3520234 3520234 single base substitution G C intron_variant BRCA-EU 19 3520234 3520234 single base substitution G C upstream_gene_variant BRCA-EU 19 3520738 3520738 single base substitution C G intron_variant BRCA-EU 19 3520738 3520738 single base substitution C G upstream_gene_variant BRCA-EU 19 3520738 3520738 single base substitution C T intron_variant BRCA-EU 19 3520738 3520738 single base substitution C T upstream_gene_variant BRCA-EU 19 3521378 3521378 single base substitution G C intron_variant BRCA-EU 19 3521378 3521378 single base substitution G C upstream_gene_variant BRCA-EU 19 3524636 3524636 single base substitution G A intron_variant BRCA-EU 19 3524636 3524636 single base substitution G A upstream_gene_variant BRCA-EU 19 3525662 3525662 single base substitution G T intron_variant BRCA-EU 19 3525662 3525662 single base substitution G T upstream_gene_variant BRCA-EU 19 3526952 3526952 single base substitution C T intron_variant BRCA-EU 19 3527168 3527168 single base substitution C T downstream_gene_variant BRCA-EU 19 3527168 3527168 single base substitution C T intron_variant BRCA-EU 19 3527393 3527393 single base substitution G C downstream_gene_variant BRCA-EU 19 3527393 3527393 single base substitution G C intron_variant BRCA-EU 19 3527403 3527403 single base substitution G A downstream_gene_variant BRCA-EU 19 3527403 3527403 single base substitution G A intron_variant BRCA-EU 19 3529126 3529126 single base substitution G A downstream_gene_variant BRCA-EU 19 3529126 3529126 single base substitution G A intron_variant BRCA-EU 19 3529126 3529126 single base substitution G A upstream_gene_variant BRCA-EU 19 3529129 3529129 single base substitution T C downstream_gene_variant BRCA-EU 19 3529129 3529129 single base substitution T C intron_variant BRCA-EU 19 3529129 3529129 single base substitution T C upstream_gene_variant BRCA-EU 19 3529132 3529132 single base substitution G T downstream_gene_variant BRCA-EU 19 3529132 3529132 single base substitution G T intron_variant BRCA-EU 19 3529132 3529132 single base substitution G T upstream_gene_variant BRCA-EU 19 3530966 3530966 single base substitution C T downstream_gene_variant BRCA-EU 19 3530966 3530966 single base substitution C T intron_variant BRCA-EU 19 3530966 3530966 single base substitution C T upstream_gene_variant BRCA-EU 19 3531231 3531231 single base substitution G C downstream_gene_variant BRCA-EU 19 3531231 3531231 single base substitution G C intron_variant BRCA-EU 19 3531231 3531231 single base substitution G C upstream_gene_variant BRCA-EU 19 3532720 3532720 single base substitution G A downstream_gene_variant BRCA-EU 19 3532720 3532720 single base substitution G A intron_variant BRCA-EU 19 3532720 3532720 single base substitution G A upstream_gene_variant BRCA-EU 19 3532892 3532892 single base substitution C A downstream_gene_variant BRCA-EU 19 3532892 3532892 single base substitution C A intron_variant BRCA-EU 19 3532892 3532892 single base substitution C A upstream_gene_variant BRCA-EU 19 3533665 3533665 single base substitution G C downstream_gene_variant BRCA-EU 19 3533665 3533665 single base substitution G C exon_variant BRCA-EU 19 3533665 3533665 single base substitution G C intron_variant BRCA-EU 19 3533665 3533665 single base substitution G C upstream_gene_variant BRCA-EU 19 3533813 3533813 single base substitution T G downstream_gene_variant BRCA-EU 19 3533813 3533813 single base substitution T G intron_variant BRCA-EU 19 3533813 3533813 single base substitution T G upstream_gene_variant BRCA-EU 19 3535773 3535773 single base substitution C T 3_prime_UTR_variant BRCA-EU 19 3535773 3535773 single base substitution C T downstream_gene_variant BRCA-EU 19 3536285 3536285 single base substitution C T 3_prime_UTR_variant BRCA-EU 19 3536285 3536285 single base substitution C T downstream_gene_variant BRCA-EU 19 3537152 3537152 single base substitution T C 3_prime_UTR_variant BRCA-EU 19 3537152 3537152 single base substitution T C downstream_gene_variant BRCA-EU 19 3537874 3537874 single base substitution C T 3_prime_UTR_variant BRCA-EU 19 3537874 3537874 single base substitution C T downstream_gene_variant BRCA-EU 19 3539959 3539959 single base substitution C A downstream_gene_variant BRCA-EU 19 3541059 3541059 single base substitution C T downstream_gene_variant BRCA-FR 19 3503845 3503845 single base substitution C T upstream_gene_variant BRCA-FR 19 3521378 3521378 single base substitution G C intron_variant BRCA-FR 19 3521378 3521378 single base substitution G C upstream_gene_variant BRCA-FR 19 3522371 3522371 single base substitution T A intron_variant BRCA-FR 19 3522371 3522371 single base substitution T A upstream_gene_variant BRCA-FR 19 3524636 3524636 single base substitution G A intron_variant BRCA-FR 19 3524636 3524636 single base substitution G A upstream_gene_variant BRCA-FR 19 3525662 3525662 single base substitution G T intron_variant BRCA-FR 19 3525662 3525662 single base substitution G T upstream_gene_variant BRCA-FR 19 3526258 3526258 single base substitution C T exon_variant BRCA-FR 19 3526258 3526258 single base substitution C T splice_region_variant BRCA-FR 19 3527393 3527393 single base substitution G C downstream_gene_variant BRCA-FR 19 3527393 3527393 single base substitution G C intron_variant BRCA-UK 19 3508175 3508175 single base substitution C T intron_variant BRCA-UK 19 3526952 3526952 single base substitution C T intron_variant BTCA-JP 19 3523010 3523010 single base substitution G A exon_variant BTCA-JP 19 3523010 3523010 single base substitution G A missense_variant R8H 23G>A BTCA-JP 19 3523010 3523010 single base substitution G A upstream_gene_variant BTCA-JP 19 3526077 3526077 single base substitution C T intron_variant BTCA-JP 19 3526077 3526077 single base substitution C T upstream_gene_variant BTCA-JP 19 3526954 3526954 single base substitution G C intron_variant BTCA-JP 19 3527699 3527699 single base substitution G A downstream_gene_variant BTCA-JP 19 3527699 3527699 single base substitution G A exon_variant BTCA-JP 19 3527699 3527699 single base substitution G A intron_variant BTCA-JP 19 3527699 3527699 single base substitution G A missense_variant A181T 541G>A BTCA-JP 19 3527699 3527699 single base substitution G A upstream_gene_variant BTCA-JP 19 3527901 3527901 single base substitution A C downstream_gene_variant BTCA-JP 19 3527901 3527901 single base substitution A C intron_variant BTCA-JP 19 3527901 3527901 single base substitution A C upstream_gene_variant CESC-US 19 3526310 3526310 single base substitution G A exon_variant CESC-US 19 3526310 3526310 single base substitution G A missense_variant E105K 313G>A CESC-US 19 3532042 3532042 single base substitution C G downstream_gene_variant CESC-US 19 3532042 3532042 single base substitution C G exon_variant CESC-US 19 3532042 3532042 single base substitution C G synonymous_variant L230L 690C>G CESC-US 19 3532042 3532042 single base substitution C G synonymous_variant L319L 957C>G CESC-US 19 3532042 3532042 single base substitution C G upstream_gene_variant CESC-US 19 3532541 3532541 single base substitution G C downstream_gene_variant CESC-US 19 3532541 3532541 single base substitution G C exon_variant CESC-US 19 3532541 3532541 single base substitution G C intron_variant CESC-US 19 3532541 3532541 single base substitution G C missense_variant D290H 868G>C CESC-US 19 3532541 3532541 single base substitution G C missense_variant D379H 1135G>C CESC-US 19 3532541 3532541 single base substitution G C upstream_gene_variant CESC-US 19 3543237 3543237 single base substitution G C downstream_gene_variant CLLE-ES 19 3529383 3529383 single base substitution C G downstream_gene_variant CLLE-ES 19 3529383 3529383 single base substitution C G intron_variant CLLE-ES 19 3529383 3529383 single base substitution C G upstream_gene_variant CLLE-ES 19 3534377 3534377 single base substitution C T downstream_gene_variant CLLE-ES 19 3534377 3534377 single base substitution C T exon_variant CLLE-ES 19 3534377 3534377 single base substitution C T intron_variant COAD-US 19 3530853 3530853 single base substitution C T downstream_gene_variant COAD-US 19 3530853 3530853 single base substitution C T missense_variant R151W 451C>T COAD-US 19 3530853 3530853 single base substitution C T missense_variant R240W 718C>T COAD-US 19 3530853 3530853 single base substitution C T splice_region_variant COAD-US 19 3530853 3530853 single base substitution C T upstream_gene_variant COAD-US 19 3531955 3531955 single base substitution C T downstream_gene_variant COAD-US 19 3531955 3531955 single base substitution C T exon_variant COAD-US 19 3531955 3531955 single base substitution C T synonymous_variant D201D 603C>T COAD-US 19 3531955 3531955 single base substitution C T synonymous_variant D290D 870C>T COAD-US 19 3531955 3531955 single base substitution C T upstream_gene_variant COAD-US 19 3534809 3534809 single base substitution T A 3_prime_UTR_variant COAD-US 19 3534809 3534809 single base substitution T A downstream_gene_variant COAD-US 19 3534809 3534809 single base substitution T A exon_variant COAD-US 19 3534809 3534809 single base substitution T A missense_variant L397H 1190T>A COAD-US 19 3534809 3534809 single base substitution T A missense_variant L486H 1457T>A COAD-US 19 3534809 3534809 single base substitution T A missense_variant L489H 1466T>A COAD-US 19 3539208 3539208 single base substitution C A downstream_gene_variant COAD-US 19 3539212 3539212 single base substitution A G downstream_gene_variant COCA-CN 19 3528854 3528854 single base substitution T C downstream_gene_variant COCA-CN 19 3528854 3528854 single base substitution T C intron_variant COCA-CN 19 3528854 3528854 single base substitution T C upstream_gene_variant COCA-CN 19 3530054 3530054 single base substitution A G downstream_gene_variant COCA-CN 19 3530054 3530054 single base substitution A G intron_variant COCA-CN 19 3530054 3530054 single base substitution A G upstream_gene_variant COCA-CN 19 3531597 3531597 single base substitution G T downstream_gene_variant COCA-CN 19 3531597 3531597 single base substitution G T intron_variant COCA-CN 19 3531597 3531597 single base substitution G T upstream_gene_variant COCA-CN 19 3534823 3534823 single base substitution A C 3_prime_UTR_variant COCA-CN 19 3534823 3534823 single base substitution A C downstream_gene_variant COCA-CN 19 3534823 3534823 single base substitution A C exon_variant COCA-CN 19 3534823 3534823 single base substitution A C synonymous_variant R402R 1204A>C COCA-CN 19 3534823 3534823 single base substitution A C synonymous_variant R491R 1471A>C COCA-CN 19 3534823 3534823 single base substitution A C synonymous_variant R494R 1480A>C EOPC-DE 19 3510889 3510889 single base substitution C T intron_variant EOPC-DE 19 3517144 3517144 single base substitution C T intron_variant EOPC-DE 19 3528686 3528686 single base substitution C T downstream_gene_variant EOPC-DE 19 3528686 3528686 single base substitution C T intron_variant EOPC-DE 19 3528686 3528686 single base substitution C T upstream_gene_variant EOPC-DE 19 3529775 3529775 single base substitution C G downstream_gene_variant EOPC-DE 19 3529775 3529775 single base substitution C G intron_variant EOPC-DE 19 3529775 3529775 single base substitution C G upstream_gene_variant EOPC-DE 19 3530342 3530342 single base substitution T G downstream_gene_variant EOPC-DE 19 3530342 3530342 single base substitution T G intron_variant EOPC-DE 19 3530342 3530342 single base substitution T G upstream_gene_variant EOPC-DE 19 3532861 3532861 single base substitution T A downstream_gene_variant EOPC-DE 19 3532861 3532861 single base substitution T A intron_variant EOPC-DE 19 3532861 3532861 single base substitution T A upstream_gene_variant EOPC-DE 19 3534616 3534616 single base substitution T G downstream_gene_variant EOPC-DE 19 3534616 3534616 single base substitution T G intron_variant ESAD-UK 19 3501338 3501338 single base substitution G C upstream_gene_variant ESAD-UK 19 3501460 3501460 single base substitution T A upstream_gene_variant ESAD-UK 19 3502692 3502692 single base substitution C T upstream_gene_variant ESAD-UK 19 3505433 3505433 single base substitution C T upstream_gene_variant ESAD-UK 19 3510269 3510269 single base substitution G C intron_variant ESAD-UK 19 3510270 3510270 single base substitution G T intron_variant ESAD-UK 19 3511965 3511965 single base substitution C G intron_variant ESAD-UK 19 3512192 3512192 single base substitution C T intron_variant ESAD-UK 19 3513069 3513069 single base substitution G A intron_variant ESAD-UK 19 3516112 3516112 single base substitution G T intron_variant ESAD-UK 19 3519117 3519117 single base substitution C T intron_variant ESAD-UK 19 3519117 3519117 single base substitution C T upstream_gene_variant ESAD-UK 19 3523253 3523253 single base substitution G A intron_variant ESAD-UK 19 3523253 3523253 single base substitution G A upstream_gene_variant ESAD-UK 19 3524492 3524492 single base substitution A T intron_variant ESAD-UK 19 3524492 3524492 single base substitution A T upstream_gene_variant ESAD-UK 19 3526764 3526764 single base substitution C T intron_variant ESAD-UK 19 3526963 3526963 single base substitution T G intron_variant ESAD-UK 19 3529359 3529359 single base substitution C T downstream_gene_variant ESAD-UK 19 3529359 3529359 single base substitution C T intron_variant ESAD-UK 19 3529359 3529359 single base substitution C T upstream_gene_variant ESAD-UK 19 3534010 3534010 single base substitution C T downstream_gene_variant ESAD-UK 19 3534010 3534010 single base substitution C T intron_variant ESAD-UK 19 3534010 3534010 single base substitution C T upstream_gene_variant ESAD-UK 19 3535364 3535364 single base substitution G A 3_prime_UTR_variant ESAD-UK 19 3535364 3535364 single base substitution G A downstream_gene_variant ESAD-UK 19 3537147 3537147 single base substitution C T 3_prime_UTR_variant ESAD-UK 19 3537147 3537147 single base substitution C T downstream_gene_variant ESAD-UK 19 3539533 3539533 single base substitution G T downstream_gene_variant ESAD-UK 19 3539845 3539845 single base substitution G C downstream_gene_variant ESAD-UK 19 3541841 3541841 single base substitution C G downstream_gene_variant ESAD-UK 19 3542978 3542978 single base substitution G A downstream_gene_variant ESCA-CN 19 3542848 3542848 single base substitution C T downstream_gene_variant GBM-US 19 3531983 3531983 single base substitution A C downstream_gene_variant GBM-US 19 3531983 3531983 single base substitution A C exon_variant GBM-US 19 3531983 3531983 single base substitution A C missense_variant T211P 631A>C GBM-US 19 3531983 3531983 single base substitution A C missense_variant T300P 898A>C GBM-US 19 3531983 3531983 single base substitution A C upstream_gene_variant GBM-US 19 3543251 3543252 deletion of <=200bp GG - downstream_gene_variant KIRC-US 19 3522955 3522955 single base substitution C A splice_region_variant KIRC-US 19 3522955 3522955 single base substitution C A upstream_gene_variant KIRC-US 19 3523035 3523035 single base substitution G C exon_variant KIRC-US 19 3523035 3523035 single base substitution G C missense_variant Q16H 48G>C KIRC-US 19 3523035 3523035 single base substitution G C upstream_gene_variant KIRC-US 19 3531748 3531748 single base substitution G A downstream_gene_variant KIRC-US 19 3531748 3531748 single base substitution G A exon_variant KIRC-US 19 3531748 3531748 single base substitution G A missense_variant V164M 490G>A KIRC-US 19 3531748 3531748 single base substitution G A missense_variant V253M 757G>A KIRC-US 19 3531748 3531748 single base substitution G A upstream_gene_variant KIRC-US 19 3532608 3532608 single base substitution A G downstream_gene_variant KIRC-US 19 3532608 3532608 single base substitution A G exon_variant KIRC-US 19 3532608 3532608 single base substitution A G missense_variant Q312R 935A>G KIRC-US 19 3532608 3532608 single base substitution A G missense_variant Q401R 1202A>G KIRC-US 19 3532608 3532608 single base substitution A G upstream_gene_variant KIRC-US 19 3533330 3533330 single base substitution C A 3_prime_UTR_variant KIRC-US 19 3533330 3533330 single base substitution C A downstream_gene_variant KIRC-US 19 3533330 3533330 single base substitution C A exon_variant KIRC-US 19 3533330 3533330 single base substitution C A synonymous_variant V338V 1014C>A KIRC-US 19 3533330 3533330 single base substitution C A synonymous_variant V427V 1281C>A KIRC-US 19 3533330 3533330 single base substitution C A upstream_gene_variant KIRC-US 19 3533336 3533336 single base substitution G A 3_prime_UTR_variant KIRC-US 19 3533336 3533336 single base substitution G A downstream_gene_variant KIRC-US 19 3533336 3533336 single base substitution G A exon_variant KIRC-US 19 3533336 3533336 single base substitution G A synonymous_variant K340K 1020G>A KIRC-US 19 3533336 3533336 single base substitution G A synonymous_variant K429K 1287G>A KIRC-US 19 3533336 3533336 single base substitution G A upstream_gene_variant KIRP-US 19 3525916 3525916 single base substitution G A exon_variant KIRP-US 19 3525916 3525916 single base substitution G A synonymous_variant S40S 120G>A KIRP-US 19 3525916 3525916 single base substitution G A upstream_gene_variant KIRP-US 19 3527659 3527659 single base substitution C A downstream_gene_variant KIRP-US 19 3527659 3527659 single base substitution C A exon_variant KIRP-US 19 3527659 3527659 single base substitution C A intron_variant KIRP-US 19 3527659 3527659 single base substitution C A synonymous_variant P167P 501C>A KIRP-US 19 3527659 3527659 single base substitution C A upstream_gene_variant LAML-KR 19 3529544 3529544 single base substitution G A downstream_gene_variant LAML-KR 19 3529544 3529544 single base substitution G A intron_variant LAML-KR 19 3529544 3529544 single base substitution G A upstream_gene_variant LAML-KR 19 3529550 3529550 single base substitution C A downstream_gene_variant LAML-KR 19 3529550 3529550 single base substitution C A intron_variant LAML-KR 19 3529550 3529550 single base substitution C A upstream_gene_variant LAML-KR 19 3530013 3530013 single base substitution T A downstream_gene_variant LAML-KR 19 3530013 3530013 single base substitution T A intron_variant LAML-KR 19 3530013 3530013 single base substitution T A upstream_gene_variant LAML-KR 19 3530342 3530342 single base substitution T G downstream_gene_variant LAML-KR 19 3530342 3530342 single base substitution T G intron_variant LAML-KR 19 3530342 3530342 single base substitution T G upstream_gene_variant LAML-KR 19 3530462 3530462 single base substitution A G downstream_gene_variant LAML-KR 19 3530462 3530462 single base substitution A G intron_variant LAML-KR 19 3530462 3530462 single base substitution A G upstream_gene_variant LAML-KR 19 3530469 3530469 single base substitution C G downstream_gene_variant LAML-KR 19 3530469 3530469 single base substitution C G intron_variant LAML-KR 19 3530469 3530469 single base substitution C G upstream_gene_variant LAML-KR 19 3530492 3530492 single base substitution G A downstream_gene_variant LAML-KR 19 3530492 3530492 single base substitution G A intron_variant LAML-KR 19 3530492 3530492 single base substitution G A upstream_gene_variant LAML-KR 19 3541082 3541082 single base substitution G A downstream_gene_variant LAML-KR 19 3541092 3541092 single base substitution G C downstream_gene_variant LGG-US 19 3532532 3532532 single base substitution G C downstream_gene_variant LGG-US 19 3532532 3532532 single base substitution G C exon_variant LGG-US 19 3532532 3532532 single base substitution G C intron_variant LGG-US 19 3532532 3532532 single base substitution G C missense_variant G287R 859G>C LGG-US 19 3532532 3532532 single base substitution G C missense_variant G376R 1126G>C LGG-US 19 3532532 3532532 single base substitution G C upstream_gene_variant LICA-FR 19 3526997 3526997 single base substitution G T exon_variant LICA-FR 19 3526997 3526997 single base substitution G T intron_variant LICA-FR 19 3526997 3526997 single base substitution G T missense_variant R136L 407G>T LICA-FR 19 3529145 3529145 single base substitution A T downstream_gene_variant LICA-FR 19 3529145 3529145 single base substitution A T intron_variant LICA-FR 19 3529145 3529145 single base substitution A T upstream_gene_variant LICA-FR 19 3529152 3529152 single base substitution A T downstream_gene_variant LICA-FR 19 3529152 3529152 single base substitution A T intron_variant LICA-FR 19 3529152 3529152 single base substitution A T upstream_gene_variant LICA-FR 19 3532525 3532525 deletion of <=200bp G - downstream_gene_variant LICA-FR 19 3532525 3532525 deletion of <=200bp G - exon_variant LICA-FR 19 3532525 3532525 deletion of <=200bp G - frameshift_variant S284 LICA-FR 19 3532525 3532525 deletion of <=200bp G - frameshift_variant S373 LICA-FR 19 3532525 3532525 deletion of <=200bp G - intron_variant LICA-FR 19 3532525 3532525 deletion of <=200bp G - upstream_gene_variant LICA-FR 19 3533382 3533382 single base substitution C G 3_prime_UTR_variant LICA-FR 19 3533382 3533382 single base substitution C G downstream_gene_variant LICA-FR 19 3533382 3533382 single base substitution C G exon_variant LICA-FR 19 3533382 3533382 single base substitution C G missense_variant R356G 1066C>G LICA-FR 19 3533382 3533382 single base substitution C G missense_variant R445G 1333C>G LICA-FR 19 3533382 3533382 single base substitution C G upstream_gene_variant LICA-FR 19 3534802 3534802 single base substitution T A 3_prime_UTR_variant LICA-FR 19 3534802 3534802 single base substitution T A downstream_gene_variant LICA-FR 19 3534802 3534802 single base substitution T A exon_variant LICA-FR 19 3534802 3534802 single base substitution T A missense_variant S395T 1183T>A LICA-FR 19 3534802 3534802 single base substitution T A missense_variant S484T 1450T>A LICA-FR 19 3534802 3534802 single base substitution T A missense_variant S487T 1459T>A LICA-FR 19 3537355 3537355 single base substitution C T 3_prime_UTR_variant LICA-FR 19 3537355 3537355 single base substitution C T downstream_gene_variant LIHC-US 19 3522996 3522996 single base substitution G A exon_variant LIHC-US 19 3522996 3522996 single base substitution G A synonymous_variant Q3Q 9G>A LIHC-US 19 3522996 3522996 single base substitution G A upstream_gene_variant LIHC-US 19 3527733 3527733 single base substitution T G downstream_gene_variant LIHC-US 19 3527733 3527733 single base substitution T G exon_variant LIHC-US 19 3527733 3527733 single base substitution T G intron_variant LIHC-US 19 3527733 3527733 single base substitution T G missense_variant L192R 575T>G LIHC-US 19 3527733 3527733 single base substitution T G upstream_gene_variant LIHC-US 19 3532454 3532454 single base substitution C T downstream_gene_variant LIHC-US 19 3532454 3532454 single base substitution C T intron_variant LIHC-US 19 3532454 3532454 single base substitution C T stop_gained Q261* 781C>T LIHC-US 19 3532454 3532454 single base substitution C T stop_gained Q350* 1048C>T LIHC-US 19 3532454 3532454 single base substitution C T upstream_gene_variant LINC-JP 19 3508385 3508385 single base substitution T G intron_variant LINC-JP 19 3526021 3526021 deletion of <=200bp C - intron_variant LINC-JP 19 3526021 3526021 deletion of <=200bp C - upstream_gene_variant LINC-JP 19 3530805 3530805 single base substitution G A downstream_gene_variant LINC-JP 19 3530805 3530805 single base substitution G A exon_variant LINC-JP 19 3530805 3530805 single base substitution G A missense_variant D135N 403G>A LINC-JP 19 3530805 3530805 single base substitution G A missense_variant D224N 670G>A LINC-JP 19 3530805 3530805 single base substitution G A upstream_gene_variant LINC-JP 19 3532356 3532356 single base substitution A G downstream_gene_variant LINC-JP 19 3532356 3532356 single base substitution A G intron_variant LINC-JP 19 3532356 3532356 single base substitution A G upstream_gene_variant LINC-JP 19 3532430 3532430 single base substitution C G downstream_gene_variant LINC-JP 19 3532430 3532430 single base substitution C G intron_variant LINC-JP 19 3532430 3532430 single base substitution C G missense_variant H253D 757C>G LINC-JP 19 3532430 3532430 single base substitution C G missense_variant H342D 1024C>G LINC-JP 19 3532430 3532430 single base substitution C G upstream_gene_variant LIRI-JP 19 3503560 3503560 single base substitution C G upstream_gene_variant LIRI-JP 19 3504293 3504293 single base substitution G A upstream_gene_variant LIRI-JP 19 3504945 3504945 single base substitution C G upstream_gene_variant LIRI-JP 19 3505164 3505164 single base substitution T C upstream_gene_variant LIRI-JP 19 3508764 3508764 single base substitution A G intron_variant LIRI-JP 19 3511013 3511013 single base substitution C T intron_variant LIRI-JP 19 3514568 3514568 single base substitution A G intron_variant LIRI-JP 19 3517270 3517270 single base substitution C G intron_variant LIRI-JP 19 3519801 3519801 single base substitution G A intron_variant LIRI-JP 19 3519801 3519801 single base substitution G A upstream_gene_variant LIRI-JP 19 3520477 3520477 single base substitution G A intron_variant LIRI-JP 19 3520477 3520477 single base substitution G A upstream_gene_variant LIRI-JP 19 3522583 3522583 single base substitution C T intron_variant LIRI-JP 19 3522583 3522583 single base substitution C T upstream_gene_variant LIRI-JP 19 3524518 3524518 single base substitution T C intron_variant LIRI-JP 19 3524518 3524518 single base substitution T C upstream_gene_variant LIRI-JP 19 3541570 3541570 single base substitution C T downstream_gene_variant LIRI-JP 19 3541957 3541957 single base substitution A G downstream_gene_variant LIRI-JP 19 3541973 3541973 single base substitution A G downstream_gene_variant LUSC-KR 19 3502138 3502138 single base substitution T A upstream_gene_variant LUSC-KR 19 3504385 3504385 single base substitution C G upstream_gene_variant LUSC-KR 19 3518099 3518099 single base substitution G T intron_variant LUSC-KR 19 3518099 3518099 single base substitution G T upstream_gene_variant LUSC-KR 19 3518763 3518763 single base substitution G T intron_variant LUSC-KR 19 3518763 3518763 single base substitution G T upstream_gene_variant LUSC-KR 19 3525246 3525246 single base substitution C T intron_variant LUSC-KR 19 3525246 3525246 single base substitution C T upstream_gene_variant LUSC-KR 19 3528731 3528731 single base substitution G A downstream_gene_variant LUSC-KR 19 3528731 3528731 single base substitution G A intron_variant LUSC-KR 19 3528731 3528731 single base substitution G A upstream_gene_variant LUSC-KR 19 3529143 3529143 single base substitution G A downstream_gene_variant LUSC-KR 19 3529143 3529143 single base substitution G A intron_variant LUSC-KR 19 3529143 3529143 single base substitution G A upstream_gene_variant LUSC-KR 19 3529145 3529145 single base substitution A T downstream_gene_variant LUSC-KR 19 3529145 3529145 single base substitution A T intron_variant LUSC-KR 19 3529145 3529145 single base substitution A T upstream_gene_variant LUSC-KR 19 3529579 3529579 single base substitution T A downstream_gene_variant LUSC-KR 19 3529579 3529579 single base substitution T A intron_variant LUSC-KR 19 3529579 3529579 single base substitution T A upstream_gene_variant LUSC-KR 19 3530193 3530193 single base substitution C T downstream_gene_variant LUSC-KR 19 3530193 3530193 single base substitution C T intron_variant LUSC-KR 19 3530193 3530193 single base substitution C T upstream_gene_variant LUSC-KR 19 3534539 3534539 single base substitution C T downstream_gene_variant LUSC-KR 19 3534539 3534539 single base substitution C T intron_variant LUSC-KR 19 3535386 3535386 single base substitution G T 3_prime_UTR_variant LUSC-KR 19 3535386 3535386 single base substitution G T downstream_gene_variant LUSC-KR 19 3536813 3536813 single base substitution G C 3_prime_UTR_variant LUSC-KR 19 3536813 3536813 single base substitution G C downstream_gene_variant LUSC-KR 19 3536852 3536852 single base substitution G A 3_prime_UTR_variant LUSC-KR 19 3536852 3536852 single base substitution G A downstream_gene_variant LUSC-KR 19 3537093 3537093 single base substitution G C 3_prime_UTR_variant LUSC-KR 19 3537093 3537093 single base substitution G C downstream_gene_variant MALY-DE 19 3516275 3516275 insertion of <=200bp - T intron_variant MALY-DE 19 3521845 3521845 single base substitution T A intron_variant MALY-DE 19 3521845 3521845 single base substitution T A upstream_gene_variant MALY-DE 19 3529145 3529145 single base substitution A T downstream_gene_variant MALY-DE 19 3529145 3529145 single base substitution A T intron_variant MALY-DE 19 3529145 3529145 single base substitution A T upstream_gene_variant MELA-AU 19 3501474 3501474 single base substitution G A upstream_gene_variant MELA-AU 19 3502005 3502005 single base substitution C T upstream_gene_variant MELA-AU 19 3502221 3502221 single base substitution C G upstream_gene_variant MELA-AU 19 3502410 3502410 single base substitution C T upstream_gene_variant MELA-AU 19 3502436 3502436 single base substitution C T upstream_gene_variant MELA-AU 19 3503189 3503189 single base substitution C T upstream_gene_variant MELA-AU 19 3503228 3503228 single base substitution C T upstream_gene_variant MELA-AU 19 3503503 3503503 single base substitution C T upstream_gene_variant MELA-AU 19 3504234 3504234 single base substitution C T upstream_gene_variant MELA-AU 19 3504345 3504345 single base substitution C T upstream_gene_variant MELA-AU 19 3504602 3504602 single base substitution G A upstream_gene_variant MELA-AU 19 3506217 3506217 single base substitution G A upstream_gene_variant MELA-AU 19 3506587 3506587 single base substitution C T intron_variant MELA-AU 19 3507528 3507528 single base substitution T A intron_variant MELA-AU 19 3507767 3507767 single base substitution G A intron_variant MELA-AU 19 3508444 3508444 single base substitution C T intron_variant MELA-AU 19 3508916 3508916 single base substitution C T intron_variant MELA-AU 19 3510957 3510957 single base substitution C T intron_variant MELA-AU 19 3511075 3511075 single base substitution C T intron_variant MELA-AU 19 3511224 3511224 single base substitution G T intron_variant MELA-AU 19 3512903 3512903 single base substitution C T intron_variant MELA-AU 19 3513260 3513260 single base substitution C T intron_variant MELA-AU 19 3514111 3514111 single base substitution C T intron_variant MELA-AU 19 3514138 3514138 single base substitution C T intron_variant MELA-AU 19 3514178 3514178 single base substitution C T intron_variant MELA-AU 19 3514549 3514549 single base substitution C T intron_variant MELA-AU 19 3514686 3514686 single base substitution C T intron_variant MELA-AU 19 3514976 3514976 single base substitution G A intron_variant MELA-AU 19 3516117 3516117 single base substitution C T intron_variant MELA-AU 19 3517634 3517634 single base substitution C T intron_variant MELA-AU 19 3518135 3518135 single base substitution C T intron_variant MELA-AU 19 3518135 3518135 single base substitution C T upstream_gene_variant MELA-AU 19 3518137 3518137 single base substitution C T intron_variant MELA-AU 19 3518137 3518137 single base substitution C T upstream_gene_variant MELA-AU 19 3518711 3518711 single base substitution C T intron_variant MELA-AU 19 3518711 3518711 single base substitution C T upstream_gene_variant MELA-AU 19 3519081 3519081 single base substitution C T intron_variant MELA-AU 19 3519081 3519081 single base substitution C T upstream_gene_variant MELA-AU 19 3519468 3519468 single base substitution G A intron_variant MELA-AU 19 3519468 3519468 single base substitution G A upstream_gene_variant MELA-AU 19 3519483 3519484 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 19 3519483 3519484 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 19 3519813 3519813 single base substitution C T intron_variant MELA-AU 19 3519813 3519813 single base substitution C T upstream_gene_variant MELA-AU 19 3519864 3519864 single base substitution C T intron_variant MELA-AU 19 3519864 3519864 single base substitution C T upstream_gene_variant MELA-AU 19 3519869 3519870 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 19 3519869 3519870 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 19 3520574 3520575 deletion of <=200bp TG - intron_variant MELA-AU 19 3520574 3520575 deletion of <=200bp TG - upstream_gene_variant MELA-AU 19 3521308 3521308 single base substitution C T intron_variant MELA-AU 19 3521308 3521308 single base substitution C T upstream_gene_variant MELA-AU 19 3521735 3521735 single base substitution T G intron_variant MELA-AU 19 3521735 3521735 single base substitution T G upstream_gene_variant MELA-AU 19 3521978 3521978 single base substitution C T intron_variant MELA-AU 19 3521978 3521978 single base substitution C T upstream_gene_variant MELA-AU 19 3522243 3522243 single base substitution C T intron_variant MELA-AU 19 3522243 3522243 single base substitution C T upstream_gene_variant MELA-AU 19 3522335 3522336 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 19 3522335 3522336 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 19 3522416 3522416 single base substitution A T intron_variant MELA-AU 19 3522416 3522416 single base substitution A T upstream_gene_variant MELA-AU 19 3522642 3522642 single base substitution C T intron_variant MELA-AU 19 3522642 3522642 single base substitution C T upstream_gene_variant MELA-AU 19 3522692 3522693 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 19 3522692 3522693 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 19 3523204 3523204 single base substitution C T intron_variant MELA-AU 19 3523204 3523204 single base substitution C T upstream_gene_variant MELA-AU 19 3523226 3523226 single base substitution C T intron_variant MELA-AU 19 3523226 3523226 single base substitution C T upstream_gene_variant MELA-AU 19 3523554 3523554 single base substitution C T intron_variant MELA-AU 19 3523554 3523554 single base substitution C T upstream_gene_variant MELA-AU 19 3524288 3524288 single base substitution C T intron_variant MELA-AU 19 3524288 3524288 single base substitution C T upstream_gene_variant MELA-AU 19 3525675 3525675 single base substitution C T intron_variant MELA-AU 19 3525675 3525675 single base substitution C T upstream_gene_variant MELA-AU 19 3525784 3525784 single base substitution C T intron_variant MELA-AU 19 3525784 3525784 single base substitution C T upstream_gene_variant MELA-AU 19 3525943 3525943 single base substitution C T exon_variant MELA-AU 19 3525943 3525943 single base substitution C T synonymous_variant I49I 147C>T MELA-AU 19 3525943 3525943 single base substitution C T upstream_gene_variant MELA-AU 19 3525944 3525944 single base substitution C T exon_variant MELA-AU 19 3525944 3525944 single base substitution C T missense_variant P50S 148C>T MELA-AU 19 3525944 3525944 single base substitution C T upstream_gene_variant MELA-AU 19 3525992 3525992 single base substitution G C splice_donor_variant MELA-AU 19 3525992 3525992 single base substitution G C upstream_gene_variant MELA-AU 19 3526192 3526192 single base substitution C T exon_variant MELA-AU 19 3526192 3526192 single base substitution C T intron_variant MELA-AU 19 3526726 3526726 single base substitution C T intron_variant MELA-AU 19 3526820 3526820 single base substitution C T intron_variant MELA-AU 19 3526931 3526932 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 19 3526982 3526982 single base substitution C T exon_variant MELA-AU 19 3526982 3526982 single base substitution C T intron_variant MELA-AU 19 3526982 3526982 single base substitution C T missense_variant S131F 392C>T MELA-AU 19 3527079 3527079 single base substitution C T downstream_gene_variant MELA-AU 19 3527079 3527079 single base substitution C T intron_variant MELA-AU 19 3527154 3527154 single base substitution C T downstream_gene_variant MELA-AU 19 3527154 3527154 single base substitution C T intron_variant MELA-AU 19 3527250 3527251 multiple base substitution (>=2bp and <=200bp) CC AT downstream_gene_variant MELA-AU 19 3527250 3527251 multiple base substitution (>=2bp and <=200bp) CC AT intron_variant MELA-AU 19 3527318 3527318 single base substitution C T downstream_gene_variant MELA-AU 19 3527318 3527318 single base substitution C T intron_variant MELA-AU 19 3527535 3527536 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 19 3527535 3527536 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 19 3527535 3527536 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 19 3527649 3527649 single base substitution C T downstream_gene_variant MELA-AU 19 3527649 3527649 single base substitution C T exon_variant MELA-AU 19 3527649 3527649 single base substitution C T intron_variant MELA-AU 19 3527649 3527649 single base substitution C T missense_variant P164L 491C>T MELA-AU 19 3527649 3527649 single base substitution C T upstream_gene_variant MELA-AU 19 3527673 3527673 single base substitution C T downstream_gene_variant MELA-AU 19 3527673 3527673 single base substitution C T exon_variant MELA-AU 19 3527673 3527673 single base substitution C T intron_variant MELA-AU 19 3527673 3527673 single base substitution C T missense_variant S172F 515C>T MELA-AU 19 3527673 3527673 single base substitution C T upstream_gene_variant MELA-AU 19 3527860 3527860 single base substitution C T downstream_gene_variant MELA-AU 19 3527860 3527860 single base substitution C T intron_variant MELA-AU 19 3527860 3527860 single base substitution C T upstream_gene_variant MELA-AU 19 3528071 3528071 single base substitution C T downstream_gene_variant MELA-AU 19 3528071 3528071 single base substitution C T intron_variant MELA-AU 19 3528071 3528071 single base substitution C T upstream_gene_variant MELA-AU 19 3528808 3528808 single base substitution G A downstream_gene_variant MELA-AU 19 3528808 3528808 single base substitution G A intron_variant MELA-AU 19 3528808 3528808 single base substitution G A upstream_gene_variant MELA-AU 19 3529889 3529889 single base substitution G T downstream_gene_variant MELA-AU 19 3529889 3529889 single base substitution G T intron_variant MELA-AU 19 3529889 3529889 single base substitution G T upstream_gene_variant MELA-AU 19 3531134 3531134 single base substitution C T downstream_gene_variant MELA-AU 19 3531134 3531134 single base substitution C T intron_variant MELA-AU 19 3531134 3531134 single base substitution C T upstream_gene_variant MELA-AU 19 3531809 3531809 single base substitution G C downstream_gene_variant MELA-AU 19 3531809 3531809 single base substitution G C exon_variant MELA-AU 19 3531809 3531809 single base substitution G C missense_variant R184P 551G>C MELA-AU 19 3531809 3531809 single base substitution G C missense_variant R273P 818G>C MELA-AU 19 3531809 3531809 single base substitution G C upstream_gene_variant MELA-AU 19 3532441 3532441 single base substitution G A downstream_gene_variant MELA-AU 19 3532441 3532441 single base substitution G A intron_variant MELA-AU 19 3532441 3532441 single base substitution G A synonymous_variant L256L 768G>A MELA-AU 19 3532441 3532441 single base substitution G A synonymous_variant L345L 1035G>A MELA-AU 19 3532441 3532441 single base substitution G A upstream_gene_variant MELA-AU 19 3532601 3532601 single base substitution G A downstream_gene_variant MELA-AU 19 3532601 3532601 single base substitution G A exon_variant MELA-AU 19 3532601 3532601 single base substitution G A missense_variant G310S 928G>A MELA-AU 19 3532601 3532601 single base substitution G A missense_variant G399S 1195G>A MELA-AU 19 3532601 3532601 single base substitution G A upstream_gene_variant MELA-AU 19 3532605 3532605 single base substitution C T downstream_gene_variant MELA-AU 19 3532605 3532605 single base substitution C T exon_variant MELA-AU 19 3532605 3532605 single base substitution C T missense_variant S311F 932C>T MELA-AU 19 3532605 3532605 single base substitution C T missense_variant S400F 1199C>T MELA-AU 19 3532605 3532605 single base substitution C T upstream_gene_variant MELA-AU 19 3532619 3532619 single base substitution C T downstream_gene_variant MELA-AU 19 3532619 3532619 single base substitution C T exon_variant MELA-AU 19 3532619 3532619 single base substitution C T synonymous_variant L316L 946C>T MELA-AU 19 3532619 3532619 single base substitution C T synonymous_variant L405L 1213C>T MELA-AU 19 3532619 3532619 single base substitution C T upstream_gene_variant MELA-AU 19 3532802 3532802 single base substitution T G downstream_gene_variant MELA-AU 19 3532802 3532802 single base substitution T G intron_variant MELA-AU 19 3532802 3532802 single base substitution T G upstream_gene_variant MELA-AU 19 3532939 3532939 single base substitution G A downstream_gene_variant MELA-AU 19 3532939 3532939 single base substitution G A intron_variant MELA-AU 19 3532939 3532939 single base substitution G A upstream_gene_variant MELA-AU 19 3534291 3534291 single base substitution C T downstream_gene_variant MELA-AU 19 3534291 3534291 single base substitution C T exon_variant MELA-AU 19 3534291 3534291 single base substitution C T intron_variant MELA-AU 19 3534622 3534622 single base substitution G A downstream_gene_variant MELA-AU 19 3534622 3534622 single base substitution G A intron_variant MELA-AU 19 3534747 3534747 single base substitution C T downstream_gene_variant MELA-AU 19 3534747 3534747 single base substitution C T intron_variant MELA-AU 19 3534919 3534920 multiple base substitution (>=2bp and <=200bp) GC AA 3_prime_UTR_variant MELA-AU 19 3534919 3534920 multiple base substitution (>=2bp and <=200bp) GC AA downstream_gene_variant MELA-AU 19 3534919 3534920 multiple base substitution (>=2bp and <=200bp) GC AA exon_variant MELA-AU 19 3535185 3535185 single base substitution G A 3_prime_UTR_variant MELA-AU 19 3535185 3535185 single base substitution G A downstream_gene_variant MELA-AU 19 3535185 3535185 single base substitution G A exon_variant MELA-AU 19 3535406 3535406 single base substitution C A 3_prime_UTR_variant MELA-AU 19 3535406 3535406 single base substitution C A downstream_gene_variant MELA-AU 19 3536393 3536393 single base substitution T A 3_prime_UTR_variant MELA-AU 19 3536393 3536393 single base substitution T A downstream_gene_variant MELA-AU 19 3536604 3536604 single base substitution G A 3_prime_UTR_variant MELA-AU 19 3536604 3536604 single base substitution G A downstream_gene_variant MELA-AU 19 3536931 3536931 single base substitution G C 3_prime_UTR_variant MELA-AU 19 3536931 3536931 single base substitution G C downstream_gene_variant MELA-AU 19 3537285 3537285 single base substitution G A 3_prime_UTR_variant MELA-AU 19 3537285 3537285 single base substitution G A downstream_gene_variant MELA-AU 19 3537743 3537743 single base substitution C T 3_prime_UTR_variant MELA-AU 19 3537743 3537743 single base substitution C T downstream_gene_variant MELA-AU 19 3537776 3537776 single base substitution G C 3_prime_UTR_variant MELA-AU 19 3537776 3537776 single base substitution G C downstream_gene_variant MELA-AU 19 3537831 3537831 single base substitution A G 3_prime_UTR_variant MELA-AU 19 3537831 3537831 single base substitution A G downstream_gene_variant MELA-AU 19 3538121 3538121 single base substitution C T 3_prime_UTR_variant MELA-AU 19 3538121 3538121 single base substitution C T downstream_gene_variant MELA-AU 19 3538205 3538205 single base substitution C T 3_prime_UTR_variant MELA-AU 19 3538205 3538205 single base substitution C T downstream_gene_variant MELA-AU 19 3538518 3538518 single base substitution A T downstream_gene_variant MELA-AU 19 3538558 3538558 single base substitution C T downstream_gene_variant MELA-AU 19 3538621 3538621 single base substitution C T downstream_gene_variant MELA-AU 19 3538705 3538705 single base substitution C T downstream_gene_variant MELA-AU 19 3538847 3538847 single base substitution C T downstream_gene_variant MELA-AU 19 3538880 3538880 single base substitution C T downstream_gene_variant MELA-AU 19 3539029 3539029 single base substitution C T downstream_gene_variant MELA-AU 19 3539061 3539061 single base substitution C T downstream_gene_variant MELA-AU 19 3539208 3539208 single base substitution C T downstream_gene_variant MELA-AU 19 3539241 3539241 single base substitution C T downstream_gene_variant MELA-AU 19 3539284 3539285 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 19 3539299 3539299 single base substitution C T downstream_gene_variant MELA-AU 19 3539396 3539396 single base substitution C T downstream_gene_variant MELA-AU 19 3539454 3539454 single base substitution T C downstream_gene_variant MELA-AU 19 3539492 3539492 single base substitution C T downstream_gene_variant MELA-AU 19 3539649 3539649 single base substitution C T downstream_gene_variant MELA-AU 19 3540731 3540731 single base substitution G A downstream_gene_variant MELA-AU 19 3540804 3540804 single base substitution G A downstream_gene_variant MELA-AU 19 3541306 3541306 single base substitution C T downstream_gene_variant MELA-AU 19 3541772 3541772 single base substitution G A downstream_gene_variant MELA-AU 19 3541794 3541794 single base substitution G A downstream_gene_variant MELA-AU 19 3542086 3542086 single base substitution G A downstream_gene_variant ORCA-IN 19 3520923 3520923 single base substitution C G intron_variant ORCA-IN 19 3520923 3520923 single base substitution C G upstream_gene_variant ORCA-IN 19 3529448 3529448 single base substitution T G downstream_gene_variant ORCA-IN 19 3529448 3529448 single base substitution T G intron_variant ORCA-IN 19 3529448 3529448 single base substitution T G upstream_gene_variant ORCA-IN 19 3530188 3530188 single base substitution T G downstream_gene_variant ORCA-IN 19 3530188 3530188 single base substitution T G intron_variant ORCA-IN 19 3530188 3530188 single base substitution T G upstream_gene_variant ORCA-IN 19 3530517 3530517 single base substitution T C downstream_gene_variant ORCA-IN 19 3530517 3530517 single base substitution T C intron_variant ORCA-IN 19 3530517 3530517 single base substitution T C upstream_gene_variant ORCA-IN 19 3543284 3543284 single base substitution G T downstream_gene_variant OV-AU 19 3510043 3510043 single base substitution G A intron_variant OV-AU 19 3526994 3526994 single base substitution A C exon_variant OV-AU 19 3526994 3526994 single base substitution A C intron_variant OV-AU 19 3526994 3526994 single base substitution A C missense_variant K135T 404A>C OV-AU 19 3528324 3528324 single base substitution C T downstream_gene_variant OV-AU 19 3528324 3528324 single base substitution C T intron_variant OV-AU 19 3528324 3528324 single base substitution C T upstream_gene_variant OV-AU 19 3530212 3530212 single base substitution G T downstream_gene_variant OV-AU 19 3530212 3530212 single base substitution G T intron_variant OV-AU 19 3530212 3530212 single base substitution G T upstream_gene_variant OV-AU 19 3541665 3541665 single base substitution G C downstream_gene_variant PACA-AU 19 3505368 3505368 single base substitution G C upstream_gene_variant PACA-AU 19 3510944 3510944 single base substitution C T intron_variant PACA-AU 19 3511405 3511405 deletion of <=200bp C - intron_variant PACA-AU 19 3513018 3513018 single base substitution C A intron_variant PACA-AU 19 3516162 3516162 single base substitution A G intron_variant PACA-AU 19 3523560 3523560 single base substitution C T intron_variant PACA-AU 19 3523560 3523560 single base substitution C T upstream_gene_variant PACA-AU 19 3524089 3524089 insertion of <=200bp - AG intron_variant PACA-AU 19 3524089 3524089 insertion of <=200bp - AG upstream_gene_variant PACA-AU 19 3532075 3532075 deletion of <=200bp G - downstream_gene_variant PACA-AU 19 3532075 3532075 deletion of <=200bp G - exon_variant PACA-AU 19 3532075 3532075 deletion of <=200bp G - frameshift_variant S241 PACA-AU 19 3532075 3532075 deletion of <=200bp G - frameshift_variant S330 PACA-AU 19 3532075 3532075 deletion of <=200bp G - upstream_gene_variant PACA-AU 19 3533073 3533073 single base substitution C T downstream_gene_variant PACA-AU 19 3533073 3533073 single base substitution C T intron_variant PACA-AU 19 3533073 3533073 single base substitution C T upstream_gene_variant PACA-AU 19 3535215 3535215 single base substitution C T 3_prime_UTR_variant PACA-AU 19 3535215 3535215 single base substitution C T downstream_gene_variant PACA-AU 19 3535215 3535215 single base substitution C T exon_variant PACA-AU 19 3535885 3535885 single base substitution A G 3_prime_UTR_variant PACA-AU 19 3535885 3535885 single base substitution A G downstream_gene_variant PACA-AU 19 3540954 3540954 single base substitution G C downstream_gene_variant PACA-CA 19 3502815 3502815 single base substitution C T upstream_gene_variant PACA-CA 19 3505698 3505698 single base substitution T C upstream_gene_variant PACA-CA 19 3507296 3507296 single base substitution C A intron_variant PACA-CA 19 3509369 3509369 single base substitution G C intron_variant PACA-CA 19 3510565 3510565 single base substitution A G intron_variant PACA-CA 19 3510868 3510868 single base substitution G A intron_variant PACA-CA 19 3519083 3519083 single base substitution G A intron_variant PACA-CA 19 3519083 3519083 single base substitution G A upstream_gene_variant PACA-CA 19 3526394 3526394 single base substitution C T intron_variant PACA-CA 19 3526665 3526665 single base substitution C G intron_variant PACA-CA 19 3529140 3529140 single base substitution A T downstream_gene_variant PACA-CA 19 3529140 3529140 single base substitution A T intron_variant PACA-CA 19 3529140 3529140 single base substitution A T upstream_gene_variant PACA-CA 19 3529466 3529466 single base substitution A G downstream_gene_variant PACA-CA 19 3529466 3529466 single base substitution A G intron_variant PACA-CA 19 3529466 3529466 single base substitution A G upstream_gene_variant PACA-CA 19 3531793 3531793 single base substitution G C downstream_gene_variant PACA-CA 19 3531793 3531793 single base substitution G C exon_variant PACA-CA 19 3531793 3531793 single base substitution G C missense_variant E179Q 535G>C PACA-CA 19 3531793 3531793 single base substitution G C missense_variant E268Q 802G>C PACA-CA 19 3531793 3531793 single base substitution G C upstream_gene_variant PACA-CA 19 3532470 3532470 single base substitution T C downstream_gene_variant PACA-CA 19 3532470 3532470 single base substitution T C intron_variant PACA-CA 19 3532470 3532470 single base substitution T C missense_variant L266P 797T>C PACA-CA 19 3532470 3532470 single base substitution T C missense_variant L355P 1064T>C PACA-CA 19 3532470 3532470 single base substitution T C upstream_gene_variant PACA-CA 19 3535184 3535184 single base substitution C T 3_prime_UTR_variant PACA-CA 19 3535184 3535184 single base substitution C T downstream_gene_variant PACA-CA 19 3535184 3535184 single base substitution C T exon_variant PAEN-AU 19 3522478 3522478 single base substitution A G intron_variant PAEN-AU 19 3522478 3522478 single base substitution A G upstream_gene_variant PAEN-IT 19 3511563 3511563 single base substitution G T intron_variant PBCA-DE 19 3504505 3504505 single base substitution C T upstream_gene_variant PBCA-DE 19 3524227 3524227 single base substitution G T intron_variant PBCA-DE 19 3524227 3524227 single base substitution G T upstream_gene_variant PBCA-DE 19 3529143 3529143 single base substitution G A downstream_gene_variant PBCA-DE 19 3529143 3529143 single base substitution G A intron_variant PBCA-DE 19 3529143 3529143 single base substitution G A upstream_gene_variant PBCA-DE 19 3529895 3529895 single base substitution A T downstream_gene_variant PBCA-DE 19 3529895 3529895 single base substitution A T intron_variant PBCA-DE 19 3529895 3529895 single base substitution A T upstream_gene_variant PBCA-DE 19 3530421 3530421 single base substitution C G downstream_gene_variant PBCA-DE 19 3530421 3530421 single base substitution C G intron_variant PBCA-DE 19 3530421 3530421 single base substitution C G upstream_gene_variant PBCA-DE 19 3530462 3530462 single base substitution A G downstream_gene_variant PBCA-DE 19 3530462 3530462 single base substitution A G intron_variant PBCA-DE 19 3530462 3530462 single base substitution A G upstream_gene_variant PBCA-DE 19 3530474 3530475 deletion of <=200bp GA - downstream_gene_variant PBCA-DE 19 3530474 3530475 deletion of <=200bp GA - intron_variant PBCA-DE 19 3530474 3530475 deletion of <=200bp GA - upstream_gene_variant PBCA-DE 19 3535870 3535870 single base substitution G A 3_prime_UTR_variant PBCA-DE 19 3535870 3535870 single base substitution G A downstream_gene_variant PBCA-DE 19 3536899 3536899 single base substitution G T 3_prime_UTR_variant PBCA-DE 19 3536899 3536899 single base substitution G T downstream_gene_variant PRAD-CA 19 3513456 3513456 single base substitution G C intron_variant PRAD-CA 19 3529145 3529145 single base substitution A T downstream_gene_variant PRAD-CA 19 3529145 3529145 single base substitution A T intron_variant PRAD-CA 19 3529145 3529145 single base substitution A T upstream_gene_variant PRAD-CA 19 3529795 3529795 single base substitution T C downstream_gene_variant PRAD-CA 19 3529795 3529795 single base substitution T C intron_variant PRAD-CA 19 3529795 3529795 single base substitution T C upstream_gene_variant PRAD-UK 19 3506576 3506576 single base substitution C G intron_variant PRAD-UK 19 3517038 3517038 single base substitution A T intron_variant PRAD-UK 19 3522278 3522278 single base substitution C T intron_variant PRAD-UK 19 3522278 3522278 single base substitution C T upstream_gene_variant PRAD-UK 19 3535038 3535038 single base substitution T C 3_prime_UTR_variant PRAD-UK 19 3535038 3535038 single base substitution T C downstream_gene_variant PRAD-UK 19 3535038 3535038 single base substitution T C exon_variant PRAD-US 19 3525878 3525878 single base substitution C T exon_variant PRAD-US 19 3525878 3525878 single base substitution C T missense_variant R28W 82C>T PRAD-US 19 3525878 3525878 single base substitution C T upstream_gene_variant PRAD-US 19 3527681 3527681 single base substitution C G downstream_gene_variant PRAD-US 19 3527681 3527681 single base substitution C G exon_variant PRAD-US 19 3527681 3527681 single base substitution C G intron_variant PRAD-US 19 3527681 3527681 single base substitution C G missense_variant P175A 523C>G PRAD-US 19 3527681 3527681 single base substitution C G upstream_gene_variant PRAD-US 19 3532474 3532474 single base substitution G A downstream_gene_variant PRAD-US 19 3532474 3532474 single base substitution G A intron_variant PRAD-US 19 3532474 3532474 single base substitution G A synonymous_variant A267A 801G>A PRAD-US 19 3532474 3532474 single base substitution G A synonymous_variant A356A 1068G>A PRAD-US 19 3532474 3532474 single base substitution G A upstream_gene_variant READ-US 19 3527642 3527642 single base substitution C T downstream_gene_variant READ-US 19 3527642 3527642 single base substitution C T exon_variant READ-US 19 3527642 3527642 single base substitution C T intron_variant READ-US 19 3527642 3527642 single base substitution C T missense_variant R162W 484C>T READ-US 19 3527642 3527642 single base substitution C T upstream_gene_variant RECA-EU 19 3501271 3501271 single base substitution G T upstream_gene_variant RECA-EU 19 3503931 3503931 single base substitution T C upstream_gene_variant RECA-EU 19 3509356 3509356 single base substitution C T intron_variant RECA-EU 19 3509672 3509672 single base substitution G A intron_variant RECA-EU 19 3534530 3534530 single base substitution A G downstream_gene_variant RECA-EU 19 3534530 3534530 single base substitution A G intron_variant RECA-EU 19 3540959 3540959 single base substitution G A downstream_gene_variant SKCA-BR 19 3502058 3502058 single base substitution G A upstream_gene_variant SKCA-BR 19 3503236 3503236 single base substitution C T upstream_gene_variant SKCA-BR 19 3505925 3505925 single base substitution G A upstream_gene_variant SKCA-BR 19 3506052 3506052 single base substitution G A upstream_gene_variant SKCA-BR 19 3511375 3511375 single base substitution C T intron_variant SKCA-BR 19 3516673 3516673 single base substitution C T intron_variant SKCA-BR 19 3521852 3521852 insertion of <=200bp - CT intron_variant SKCA-BR 19 3521852 3521852 insertion of <=200bp - CT upstream_gene_variant SKCA-BR 19 3524711 3524711 single base substitution A G intron_variant SKCA-BR 19 3524711 3524711 single base substitution A G upstream_gene_variant SKCA-BR 19 3528515 3528515 insertion of <=200bp - CTG downstream_gene_variant SKCA-BR 19 3528515 3528515 insertion of <=200bp - CTG intron_variant SKCA-BR 19 3528515 3528515 insertion of <=200bp - CTG upstream_gene_variant SKCA-BR 19 3528622 3528622 insertion of <=200bp - TGAGTGGATGGGA downstream_gene_variant SKCA-BR 19 3528622 3528622 insertion of <=200bp - TGAGTGGATGGGA intron_variant SKCA-BR 19 3528622 3528622 insertion of <=200bp - TGAGTGGATGGGA upstream_gene_variant SKCA-BR 19 3530532 3530532 single base substitution T G downstream_gene_variant SKCA-BR 19 3530532 3530532 single base substitution T G intron_variant SKCA-BR 19 3530532 3530532 single base substitution T G upstream_gene_variant SKCA-BR 19 3530995 3530995 single base substitution C T downstream_gene_variant SKCA-BR 19 3530995 3530995 single base substitution C T intron_variant SKCA-BR 19 3530995 3530995 single base substitution C T upstream_gene_variant SKCA-BR 19 3531636 3531636 single base substitution C T downstream_gene_variant SKCA-BR 19 3531636 3531636 single base substitution C T intron_variant SKCA-BR 19 3531636 3531636 single base substitution C T upstream_gene_variant SKCA-BR 19 3538488 3538488 single base substitution C T downstream_gene_variant SKCA-BR 19 3540094 3540094 single base substitution T C downstream_gene_variant SKCA-BR 19 3540263 3540263 insertion of <=200bp - GT downstream_gene_variant SKCA-BR 19 3540613 3540613 single base substitution C T downstream_gene_variant SKCA-BR 19 3540857 3540857 single base substitution G A downstream_gene_variant SKCA-BR 19 3541336 3541336 single base substitution A C downstream_gene_variant SKCA-BR 19 3542737 3542737 single base substitution T C downstream_gene_variant SKCA-BR 19 3542739 3542739 single base substitution C T downstream_gene_variant SKCA-BR 19 3542740 3542740 single base substitution C T downstream_gene_variant SKCA-BR 19 3542957 3542957 single base substitution C A downstream_gene_variant SKCM-US 19 3523026 3523026 single base substitution C T exon_variant SKCM-US 19 3523026 3523026 single base substitution C T synonymous_variant I13I 39C>T SKCM-US 19 3523026 3523026 single base substitution C T upstream_gene_variant SKCM-US 19 3525944 3525944 single base substitution C T exon_variant SKCM-US 19 3525944 3525944 single base substitution C T missense_variant P50S 148C>T SKCM-US 19 3525944 3525944 single base substitution C T upstream_gene_variant SKCM-US 19 3526174 3526174 single base substitution C A exon_variant SKCM-US 19 3526174 3526174 single base substitution C A missense_variant N84K 252C>A SKCM-US 19 3526983 3526983 single base substitution C T exon_variant SKCM-US 19 3526983 3526983 single base substitution C T intron_variant SKCM-US 19 3526983 3526983 single base substitution C T synonymous_variant S131S 393C>T SKCM-US 19 3527037 3527037 single base substitution C T exon_variant SKCM-US 19 3527037 3527037 single base substitution C T intron_variant SKCM-US 19 3527037 3527037 single base substitution C T synonymous_variant S149S 447C>T SKCM-US 19 3527673 3527673 single base substitution C T downstream_gene_variant SKCM-US 19 3527673 3527673 single base substitution C T exon_variant SKCM-US 19 3527673 3527673 single base substitution C T intron_variant SKCM-US 19 3527673 3527673 single base substitution C T missense_variant S172F 515C>T SKCM-US 19 3527673 3527673 single base substitution C T upstream_gene_variant SKCM-US 19 3527686 3527686 single base substitution C T downstream_gene_variant SKCM-US 19 3527686 3527686 single base substitution C T exon_variant SKCM-US 19 3527686 3527686 single base substitution C T intron_variant SKCM-US 19 3527686 3527686 single base substitution C T synonymous_variant F176F 528C>T SKCM-US 19 3527686 3527686 single base substitution C T upstream_gene_variant SKCM-US 19 3527745 3527745 single base substitution C T downstream_gene_variant SKCM-US 19 3527745 3527745 single base substitution C T exon_variant SKCM-US 19 3527745 3527745 single base substitution C T intron_variant SKCM-US 19 3527745 3527745 single base substitution C T missense_variant S196L 587C>T SKCM-US 19 3527745 3527745 single base substitution C T upstream_gene_variant SKCM-US 19 3527749 3527749 single base substitution C A downstream_gene_variant SKCM-US 19 3527749 3527749 single base substitution C A exon_variant SKCM-US 19 3527749 3527749 single base substitution C A intron_variant SKCM-US 19 3527749 3527749 single base substitution C A synonymous_variant S197S 591C>A SKCM-US 19 3527749 3527749 single base substitution C A upstream_gene_variant SKCM-US 19 3527806 3527806 single base substitution C T downstream_gene_variant SKCM-US 19 3527806 3527806 single base substitution C T exon_variant SKCM-US 19 3527806 3527806 single base substitution C T intron_variant SKCM-US 19 3527806 3527806 single base substitution C T synonymous_variant T216T 648C>T SKCM-US 19 3527806 3527806 single base substitution C T upstream_gene_variant SKCM-US 19 3532524 3532524 insertion of <=200bp - G downstream_gene_variant SKCM-US 19 3532524 3532524 insertion of <=200bp - G exon_variant SKCM-US 19 3532524 3532524 insertion of <=200bp - G frameshift_variant S284C? SKCM-US 19 3532524 3532524 insertion of <=200bp - G frameshift_variant S373C? SKCM-US 19 3532524 3532524 insertion of <=200bp - G intron_variant SKCM-US 19 3532524 3532524 insertion of <=200bp - G upstream_gene_variant SKCM-US 19 3533377 3533377 single base substitution C T 3_prime_UTR_variant SKCM-US 19 3533377 3533377 single base substitution C T downstream_gene_variant SKCM-US 19 3533377 3533377 single base substitution C T exon_variant SKCM-US 19 3533377 3533377 single base substitution C T missense_variant S354F 1061C>T SKCM-US 19 3533377 3533377 single base substitution C T missense_variant S443F 1328C>T SKCM-US 19 3533377 3533377 single base substitution C T upstream_gene_variant SKCM-US 19 3542858 3542858 insertion of <=200bp - G downstream_gene_variant SKCM-US 19 3542860 3542860 single base substitution G A downstream_gene_variant SKCM-US 19 3542863 3542863 single base substitution G A downstream_gene_variant SKCM-US 19 3542865 3542865 insertion of <=200bp - T downstream_gene_variant STAD-US 19 3523010 3523010 single base substitution G A exon_variant STAD-US 19 3523010 3523010 single base substitution G A missense_variant R8H 23G>A STAD-US 19 3523010 3523010 single base substitution G A upstream_gene_variant STAD-US 19 3523019 3523019 single base substitution G A exon_variant STAD-US 19 3523019 3523019 single base substitution G A missense_variant R11H 32G>A STAD-US 19 3523019 3523019 single base substitution G A upstream_gene_variant STAD-US 19 3525967 3525967 single base substitution G C exon_variant STAD-US 19 3525967 3525967 single base substitution G C missense_variant W57C 171G>C STAD-US 19 3525967 3525967 single base substitution G C upstream_gene_variant STAD-US 19 3527008 3527008 single base substitution G A exon_variant STAD-US 19 3527008 3527008 single base substitution G A intron_variant STAD-US 19 3527008 3527008 single base substitution G A missense_variant D140N 418G>A STAD-US 19 3527034 3527034 single base substitution C G exon_variant STAD-US 19 3527034 3527034 single base substitution C G intron_variant STAD-US 19 3527034 3527034 single base substitution C G stop_gained Y148* 444C>G STAD-US 19 3532075 3532075 deletion of <=200bp G - downstream_gene_variant STAD-US 19 3532075 3532075 deletion of <=200bp G - exon_variant STAD-US 19 3532075 3532075 deletion of <=200bp G - frameshift_variant S241 STAD-US 19 3532075 3532075 deletion of <=200bp G - frameshift_variant S330 STAD-US 19 3532075 3532075 deletion of <=200bp G - upstream_gene_variant STAD-US 19 3532525 3532525 deletion of <=200bp G - downstream_gene_variant STAD-US 19 3532525 3532525 deletion of <=200bp G - exon_variant STAD-US 19 3532525 3532525 deletion of <=200bp G - frameshift_variant S284 STAD-US 19 3532525 3532525 deletion of <=200bp G - frameshift_variant S373 STAD-US 19 3532525 3532525 deletion of <=200bp G - intron_variant STAD-US 19 3532525 3532525 deletion of <=200bp G - upstream_gene_variant STAD-US 19 3533300 3533300 single base substitution G T 3_prime_UTR_variant STAD-US 19 3533300 3533300 single base substitution G T downstream_gene_variant STAD-US 19 3533300 3533300 single base substitution G T exon_variant STAD-US 19 3533300 3533300 single base substitution G T synonymous_variant T328T 984G>T STAD-US 19 3533300 3533300 single base substitution G T synonymous_variant T417T 1251G>T STAD-US 19 3533300 3533300 single base substitution G T upstream_gene_variant STAD-US 19 3542859 3542859 deletion of <=200bp G - downstream_gene_variant THCA-SA 19 3534842 3534842 single base substitution G A 3_prime_UTR_variant THCA-SA 19 3534842 3534842 single base substitution G A downstream_gene_variant THCA-SA 19 3534842 3534842 single base substitution G A exon_variant THCA-SA 19 3535383 3535383 single base substitution C T 3_prime_UTR_variant THCA-SA 19 3535383 3535383 single base substitution C T downstream_gene_variant THCA-US 19 3523039 3523039 single base substitution G A exon_variant THCA-US 19 3523039 3523039 single base substitution G A missense_variant E18K 52G>A THCA-US 19 3523039 3523039 single base substitution G A upstream_gene_variant UCEC-US 19 3525880 3525880 single base substitution G A exon_variant UCEC-US 19 3525880 3525880 single base substitution G A synonymous_variant R28R 84G>A UCEC-US 19 3525880 3525880 single base substitution G A upstream_gene_variant UCEC-US 19 3526277 3526281 deletion of <=200bp CTGCT - exon_variant UCEC-US 19 3526277 3526281 deletion of <=200bp CTGCT - frameshift_variant LL94 UCEC-US 19 3530794 3530794 single base substitution C T downstream_gene_variant UCEC-US 19 3530794 3530794 single base substitution C T exon_variant UCEC-US 19 3530794 3530794 single base substitution C T missense_variant T131M 392C>T UCEC-US 19 3530794 3530794 single base substitution C T missense_variant T220M 659C>T UCEC-US 19 3530794 3530794 single base substitution C T upstream_gene_variant UCEC-US 19 3533342 3533342 single base substitution C A 3_prime_UTR_variant UCEC-US 19 3533342 3533342 single base substitution C A downstream_gene_variant UCEC-US 19 3533342 3533342 single base substitution C A exon_variant UCEC-US 19 3533342 3533342 single base substitution C A synonymous_variant P342P 1026C>A UCEC-US 19 3533342 3533342 single base substitution C A synonymous_variant P431P 1293C>A UCEC-US 19 3533342 3533342 single base substitution C A upstream_gene_variant UCEC-US 19 3542923 3542923 single base substitution G T downstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-C8-A274-01 COSM1479030 c.1875_1876insT p.T627fs*36 Insertion - Frameshift 16:68822164-68822165 + PD4985a COSM19780 c.763C>T p.Q255* Substitution - Nonsense 16:68810272-68810272 + SK-BR-3 COSM19832 c.?_?del? p.? Unknown XHDG07C COSM4770169 c.1417delT p.F473fs*9 Deletion - Frameshift 19:3534490-3534490 + 16 COSM1659154 c.1162G>T p.E388* Substitution - Nonsense 16:68813337-68813337 + ESCC-F77 COSM5048626 c.1273G>A p.V425I Substitution - Missense 16:68813448-68813448 + PD5961a COSM19503 c.67C>T p.Q23* Substitution - Nonsense 16:68738315-68738315 + pfg346T COSM4756927 c.1028T>A p.L343Q Substitution - Missense 16:68812154-68812154 + PD6016a2 COSM5752678 c.204T>A p.Y68* Substitution - Nonsense 16:68801710-68801710 + PD11376a COSM5752535 c.388-1G>C p.? Unknown 16:68808423-68808423 + 1530066 COSM19758 c.1774G>A p.A592T Substitution - Missense 16:68822063-68822063 + 15721 COSM5029230 c.1989_1995delCAAAATC p.Y663fs*1 Deletion - Frameshift 16:68823451-68823457 + pfg143T COSM3197047 c.1119delG p.G375fs*14 Deletion - Frameshift 19:3532527-3532527 + CHC1704T COSM4804143 c.407G>T p.R136L Substitution - Missense 19:3526999-3526999 + TCGA-GM-A4E0-01 COSM5833140 c.430delA p.N144fs*71 Deletion - Frameshift 16:68808466-68808466 + SJDES011-R COSM4579193 c.1277C>A p.T426N Substitution - Missense 16:68813452-68813452 + TCGA-DO-A2HM-01 COSM3371257 c.52G>A p.E18K Substitution - Missense 19:3523041-3523041 + CRC-26T COSM5482791 c.1471A>C p.R491R Substitution - coding silent 19:3534825-3534825 + TCGA-04-1337-01 COSM77445 c.946A>G p.M316V Substitution - Missense 16:68811797-68811797 + JROECL50 COSM19819 c.357delG p.H121fs*94 Deletion - Frameshift 16:68801863-68801863 + 4 COSM1659130 c.1778delC p.I594fs*19 Deletion - Frameshift 16:68822067-68822067 + TCGA-F5-6814-01 COSM3421114 c.628G>T p.E210* Substitution - Nonsense 16:68808789-68808789 + TCGA-CD-5799-01 COSM4062183 c.1199A>T p.D400V Substitution - Missense 16:68813374-68813374 + 986 COSM19488 c.?_?insC p.?fs Insertion - Frameshift 127T COSM5576006 c.810C>G p.H270Q Substitution - Missense 19:3531803-3531803 + 1001632 COSM20821 c.1008delG p.S337fs*19 Deletion - Frameshift 16:68811859-68811859 + OCUB-F COSM19504 c.49_163del115 p.V17fs*1 Deletion - Frameshift 16:68738297-68738411 + 996890 COSM19755 c.577A>C p.T193P Substitution - Missense 16:68808738-68808738 + pfg181T COSM19494 c.372delC p.P126fs*89 Deletion - Frameshift 16:68801878-68801878 + EGC3 COSM5055032 c.641T>C p.L214P Substitution - Missense 16:68808802-68808802 + B88-Tumor COSM1749723 c.2191C>T p.L731F Substitution - Missense 16:68828200-68828200 + Pa29C COSM19826 c.532-1G>C p.? Unknown 16:68808692-68808692 + T3058 COSM4384876 c.269G>A p.R90Q Substitution - Missense 16:68801775-68801775 + T2959 COSM4670768 c.2498T>A p.F833Y Substitution - Missense 16:68833348-68833348 + TCGA-DD-A4NK-01 COSM4935145 c.560A>G p.K187R Substitution - Missense 16:68808721-68808721 + TCGA-D8-A1Y1-01 COSM1479032 c.1936+1G>T p.? Unknown 16:68822226-68822226 + TCGA-BR-4280-01 COSM4076892 c.444C>G p.Y148* Substitution - Nonsense 19:3527036-3527036 + PD4194a COSM5774437 c.89C>G p.P30R Substitution - Missense 16:68738337-68738337 + 1001724 COSM20834 c.612_620delCTTTATTAT p.F205_I207delFII Deletion - In frame 16:68808773-68808781 + 1001724 COSM20796 c.1138_1320del183 p.Y380_K440del61 Deletion - In frame 16:68813313-68813495 + TCGA-AC-A3BB-01 COSM19503 c.67C>T p.Q23* Substitution - Nonsense 16:68738315-68738315 + TCGA-A7-A4SB-01 COSM5833150 c.1803_1804insT p.C603fs*2 Insertion - Frameshift 16:68822092-68822093 + 996871 COSM19753 c.1009-1G>A p.? Unknown 16:68812134-68812134 + TCGA-AR-A1AL-01 COSM435601 c.1511delA p.I505fs*17 Deletion - Frameshift 16:68815705-68815705 + TCGA-DG-A2KL-01 COSM4851350 c.1135G>C p.D379H Substitution - Missense 19:3532543-3532543 + TCGA-06-1804-01 COSM3748053 c.898A>C p.T300P Substitution - Missense 19:3531985-3531985 + T2932 COSM972806 c.2521G>A p.E841K Substitution - Missense 16:68833371-68833371 + TCGA-A2-A3KC-01 COSM5833155 c.2243delC p.R749fs*21 Deletion - Frameshift 16:68828252-68828252 + 18091 COSM5029224 c.1026_1028delCCT p.L343delL Deletion - In frame 16:68812152-68812154 + TCGA-CM-6171-01 COSM1392388 c.718C>T p.R240W Substitution - Missense 19:3530855-3530855 + pfg181T COSM4748923 c.734C>T p.A245V Substitution - Missense 19:3531727-3531727 + 110 COSM3733197 c.? p.P373L Substitution - Missense CSB14 COSM1640536 c.379delC p.H128fs*87 Deletion - Frameshift 16:68801885-68801885 + DM16 COSM5608066 c.1321G>A p.G441S Substitution - Missense 16:68815515-68815515 + TCGA-H4-A2HQ-01 COSM1302174 c.337A>G p.K113E Substitution - Missense 16:68801843-68801843 + 1001630 COSM20820 c.1010_1011insA p.S337fs*13 Insertion - Frameshift 16:68812136-68812137 + PD13306a COSM5752199 c.410delC p.A137fs*78 Deletion - Frameshift 16:68808446-68808446 + BT407 COSM19539 c.2044_2062del19 p.E682fs*34 Deletion - Frameshift 16:68823506-68823524 + 993001 COSM19513 c.1676G>A p.S559N Substitution - Missense 16:68819390-68819390 + 1001712 COSM20777 c.864C>T p.D288D Substitution - coding silent 16:68811715-68811715 + T2269 COSM4670767 c.2193T>C p.L731L Substitution - coding silent 16:68828202-68828202 + TCGA-EK-A2RN-01 COSM4823145 c.313G>A p.E105K Substitution - Missense 19:3526312-3526312 + TCGA-E9-A2JT-01 COSM143801 c.1204G>C p.D402H Substitution - Missense 16:68813379-68813379 + WA26 COSM239247 c.1297G>A p.D433N Substitution - Missense 16:68813472-68813472 + Pat_40_A COSM5855455 c.703G>A p.V235M Substitution - Missense 19:3530840-3530840 + CSB1 COSM5028162 c.1578G>A p.W526* Substitution - Nonsense 16:68819292-68819292 + CHC798T COSM4958330 c.2277A>C p.G759G Substitution - coding silent 16:68828286-68828286 + 6115251 COSM5563880 c.2017C>T p.Q673* Substitution - Nonsense 16:68823479-68823479 + T2944 COSM4686010 c.1161G>A p.T387T Substitution - coding silent 19:3532569-3532569 + PD5961a COSM19503 c.67C>T p.Q23* Substitution - Nonsense 16:68738315-68738315 + S07-16280-TP COSM4990897 c.2287G>A p.E763K Substitution - Missense 16:68828296-68828296 + PD6016a2 COSM5752678 c.204T>A p.Y68* Substitution - Nonsense 16:68801710-68801710 + TCGA-AC-A23G-01 COSM3818349 c.1036C>T p.Q346* Substitution - Nonsense 16:68812162-68812162 + EVSA-T COSM19825 c.687+1_687+2delGT p.? Unknown 16:68808849-68808850 + PD14465a COSM5752253 c.651_652delAG p.E218fs*4 Deletion - Frameshift 16:68808812-68808813 + 996873 COSM19752 c.1000G>C p.D334H Substitution - Missense 16:68811851-68811851 + 996699 COSM19745 c.2512A>G p.S838G Substitution - Missense 16:68833362-68833362 + PD9067a COSM5801342 c.79_80insC p.C28fs*6 Insertion - Frameshift 16:68738327-68738328 + S00936 COSM309986 c.2204C>T p.A735V Substitution - Missense 16:68828213-68828213 + TCGA-EW-A1J5-01 COSM1479026 c.1496_1497insG p.F499fs*38 Insertion - Frameshift 16:68815690-68815691 + 996888 COSM19756 c.1320+26A>T p.? Unknown 16:68813521-68813521 + Gp5D COSM19494 c.372delC p.P126fs*89 Deletion - Frameshift 16:68801878-68801878 + TCGA-LQ-A4E4-01 COSM3818351 c.1226G>A p.W409* Substitution - Nonsense 16:68813401-68813401 + PD7204a COSM5801796 c.343_344insA p.T115fs*53 Insertion - Frameshift 16:68801849-68801850 + 1001725 COSM20835 c.1793G>A p.R598Q Substitution - Missense 16:68822082-68822082 + D-05 COSM1379150 c.769G>A p.D257N Substitution - Missense 16:68810278-68810278 + CCRF-CEM COSM1680511 c.1451C>T p.S484F Substitution - Missense 19:3534805-3534805 + HCT116 COSM3197028 c.209C>T p.S70F Substitution - Missense 19:3526133-3526133 + PTC_212 COSM5958388 c.105G>C p.E35D Substitution - Missense 16:68738353-68738353 + CAL33 COSM4593024 c.947T>G p.V316G Substitution - Missense 19:3532034-3532034 + BHY COSM4593024 c.947T>G p.V316G Substitution - Missense 19:3532034-3532034 + TCGA-AO-A0J9-01 COSM435603 c.1551delG p.E518fs*4 Deletion - Frameshift 16:68815745-68815745 + 999885 COSM19752 c.1000G>C p.D334H Substitution - Missense 16:68811851-68811851 + 997332 COSM19780 c.763C>T p.Q255* Substitution - Nonsense 16:68810272-68810272 + HCC109T COSM5816792 c.843G>A p.V281V Substitution - coding silent 16:68811694-68811694 + BT887 COSM19530 c.? p.? Unknown MDA-N COSM1680510 c.1440+8G>A p.? Unknown 19:3534521-3534521 + KM12 COSM4612773 c.989_990insG p.N333fs*47 Insertion - Frameshift 19:3532076-3532077 + 1001722 COSM20832 c.367C>T p.H123Y Substitution - Missense 16:68801873-68801873 + 1988945 COSM1651751 c.712A>G p.N238D Substitution - Missense 16:68810221-68810221 + 2218463 COSM4421279 c.1057G>T p.E353* Substitution - Nonsense 19:3532465-3532465 + 1001727 COSM20837 c.2029delC p.Q677fs*2 Deletion - Frameshift 16:68823491-68823491 + 997335 COSM19835 c.? p.??>* Substitution - Nonsense 57 COSM20791 c.862_867GACGCG>A p.D288fs*3 Complex - frameshift 16:68811713-68811718 + TCGA-B5-A0JY-01 COSM972782 c.671G>A p.R224H Substitution - Missense 16:68808832-68808832 + TCGA-DY-A1H8-01 COSM1564524 c.484C>T p.R162W Substitution - Missense 19:3527644-3527644 + T3152 COSM4686004 c.40G>A p.V14I Substitution - Missense 19:3523029-3523029 + HCT-116 COSM1684458 c.360delG p.H121fs*94 Deletion - Frameshift 16:68801866-68801866 + TCGA-AR-A1AT-01 COSM5211861 c.940delA p.N315fs*41 Deletion - Frameshift 16:68811791-68811791 + BICR_22 COSM4593023 c.947T>G p.V316G Substitution - Missense 19:3532034-3532034 + TCGA-G9-6365-01 COSM1128899 c.1136C>T p.T379M Substitution - Missense 16:68812262-68812262 + KM12 COSM3197017 c.90C>T p.T30T Substitution - coding silent 19:3525888-3525888 + 1515 COSM19491 c.?_?insT p.?fs Insertion - Frameshift tumor_4149246 COSM2996757 c.780C>T p.P260P Substitution - coding silent 16:68810289-68810289 + pfg153T COSM4756922 c.469G>T p.V157F Substitution - Missense 16:68808505-68808505 + pfg321T COSM4765271 c.204_205insT p.S70fs*24 Insertion - Frameshift 16:68801710-68801711 + PD18748a COSM5752273 c.1delA p.? Unknown 16:68737409-68737416 + 999881 COSM19746 c.1742T>C p.L581P Substitution - Missense 16:68822031-68822031 + SM12 COSM166359 c.? p.P126fs*89 Unknown TCGA-BS-A0UA-01 COSM972800 c.2195G>A p.R732Q Substitution - Missense 16:68828204-68828204 + 1530120 COSM96854 c.172G>T p.E58* Substitution - Nonsense 16:68801678-68801678 + 1530100 COSM96850 c.1966_1987del22 p.M656fs*16 Deletion - Frameshift 16:68823428-68823449 + TCGA-G9-6351-01 COSM1728427 c.1333C>A p.R445S Substitution - Missense 19:3533384-3533384 + 8015299 COSM3771994 c.1929C>T p.N643N Substitution - coding silent 16:68822218-68822218 + 1001674 COSM20825 c.1320+1delG p.? Unknown 16:68813496-68813496 + 17494 COSM1479036 c.2165-1G>T p.? Unknown 16:68828173-68828173 + 18156 COSM5029220 c.625_626delAG p.E210fs*12 Deletion - Frameshift 16:68808786-68808787 + pfg097T COSM4756923 c.531+1G>A p.? Unknown 16:68808568-68808568 + PD11740a COSM19759 c.781G>T p.E261* Substitution - Nonsense 16:68810290-68810290 + pfg346T COSM972800 c.2195G>A p.R732Q Substitution - Missense 16:68828204-68828204 + NB-0072 COSM1285093 c.1354_1355insC p.D454fs*1 Insertion - Frameshift 19:3534427-3534428 + ESCC_141 COSM3197042 c.1041C>T p.P347P Substitution - coding silent 19:3532449-3532449 + pfg349T COSM4756926 c.668A>T p.E223V Substitution - Missense 16:68808829-68808829 + 40M COSM5584743 c.75G>A p.P25P Substitution - coding silent 16:68738323-68738323 + PD8618a COSM5752695 c.2295+5G>T p.? Unknown 16:68828309-68828309 + 13 COSM1659133 c.926_960del35 p.P309fs*29 Deletion - Frameshift 16:68811777-68811811 + CSCC-15-T COSM3532354 c.148C>T p.P50S Substitution - Missense 19:3525946-3525946 + TCGA-D7-8574-01 COSM19540 c.532-1G>T p.? Unknown 16:68808692-68808692 + TCGA-A2-A1G0-01 COSM1479038 c.2600A>G p.N867S Substitution - Missense 16:68833450-68833450 + 997334 COSM19782 c.770A>G p.D257G Substitution - Missense 16:68810279-68810279 + TCGA-F4-6463-01 COSM3692626 c.1457T>A p.L486H Substitution - Missense 19:3534811-3534811 + TCGA-G2-A3IE-01 COSM1302175 c.727G>C p.E243Q Substitution - Missense 16:68810236-68810236 + TCGA-DK-A3WW-01 COSM3796943 c.454C>A p.P152T Substitution - Missense 19:3527046-3527046 + 16 COSM3735510 c.1251T>G p.N417K Substitution - Missense 16:68813426-68813426 + 17233 COSM5029227 c.1835_1836insA p.N613fs*4 Insertion - Frameshift 16:68822124-68822125 + 58T COSM5575810 c.1205A>T p.D402V Substitution - Missense 16:68813380-68813380 + 996868 COSM19748 c.1108G>C p.D370H Substitution - Missense 16:68812234-68812234 + TCGA-IN-7808-01 COSM4062181 c.895G>T p.A299S Substitution - Missense 16:68811746-68811746 + TCGA-BP-4774-01 COSM3362798 c.1202A>G p.Q401R Substitution - Missense 19:3532610-3532610 + TCGA-AA-3713-01 COSM5828851 c.870C>T p.D290D Substitution - coding silent 19:3531957-3531957 + pfg220T COSM4756925 c.614T>C p.F205S Substitution - Missense 16:68808775-68808775 + GC_307T-GC_307N COSM1247780 c.760G>A p.D254N Substitution - Missense 16:68810269-68810269 + BCT78 COSM19496 c.864_865delCG p.A289fs*3 Deletion - Frameshift 16:68811715-68811716 + pfg310T COSM20830 c.1320+1G>T p.? Unknown 16:68813496-68813496 + PD4196a COSM159882 c.1569T>G p.Y523* Substitution - Nonsense 16:68819283-68819283 + CHC2034T COSM4789846 c.1959G>T p.K653N Substitution - Missense 16:68823421-68823421 + TCGA-F4-6463-01 COSM5171395 c.1466T>A p.L489H Substitution - Missense 19:3534811-3534811 + TCGA-AA-3821-01 COSM294225 c.1093G>A p.V365I Substitution - Missense 16:68812219-68812219 + 587224 COSM1200400 c.641T>G p.L214R Substitution - Missense 16:68808802-68808802 + SM12 COSM166361 c.? p.201fs*14 Unknown 992973 COSM19500 c.2537G>C p.S846T Substitution - Missense 16:68833387-68833387 + BD57T COSM5511273 c.23G>A p.R8H Substitution - Missense 19:3523012-3523012 + BD57T COSM4076871 c.23G>A p.R8H Substitution - Missense 19:3523012-3523012 + pfg181T COSM4747419 c.271delT p.H92fs*25 Deletion - Frameshift 16:68801777-68801777 + 213T COSM5576263 c.466T>A p.W156R Substitution - Missense 16:68808502-68808502 + PD11375a COSM5752168 c.2532_2533delTC p.L845fs*15 Deletion - Frameshift 16:68833382-68833383 + TCGA-B5-A0JZ-01 COSM994819 c.1042G>A p.V348M Substitution - Missense 19:3532450-3532450 + PD13763a COSM5752580 c.26C>A p.S9* Substitution - Nonsense 16:68737441-68737441 + LIM2551 COSM4613898 c.1383delT p.F462fs*19 Deletion - Frameshift 16:68815577-68815577 + TCGA-MS-A51U-01 COSM3818352 c.1339A>T p.K447* Substitution - Nonsense 16:68815533-68815533 + TCGA-AA-A00N-01 COSM274463 c.871G>A p.D291N Substitution - Missense 16:68811722-68811722 + 1001650 COSM20823 c.1198_1200delGAT p.D400delD Deletion - In frame 16:68813373-68813375 + PD9579a COSM4756923 c.531+1G>A p.? Unknown 16:68808568-68808568 + LIM2551 COSM4613899 c.1472_1473delAG p.R492fs*44 Deletion - Frameshift 16:68815666-68815667 + TCGA-AC-A5XS-01 COSM5833153 c.2188_2191delTTTC p.L731fs*38 Deletion - Frameshift 16:68828197-68828200 + 61 COSM5741349 c.782G>T p.G261V Substitution - Missense 19:3531775-3531775 + TCGA-BR-4188-01 COSM2996751 c.635G>A p.G212E Substitution - Missense 16:68808796-68808796 + HCC18T COSM1609555 c.427C>T p.P143S Substitution - Missense 16:68808463-68808463 + 16313 COSM5029234 c.2393_2394delTT p.L798fs*8 Deletion - Frameshift 16:68829751-68829752 + BD236T COSM5519580 c.541G>A p.A181T Substitution - Missense 19:3527701-3527701 + YURIMO COSM1686278 c.263G>T p.G88V Substitution - Missense 19:3526262-3526262 + HCC076T COSM5822123 c.1666G>T p.V556L Substitution - Missense 16:68819380-68819380 + BT684 COSM19540 c.532-1G>T p.? Unknown 16:68808692-68808692 + TCGA-E2-A2P5-01 COSM3818350 c.1147C>T p.Q383* Substitution - Nonsense 16:68813322-68813322 + TCGA-BR-6566-01 COSM435590 c.688-1G>A p.? Unknown 16:68810196-68810196 + GC_314T-GC_314N COSM4771810 c.863A>T p.D288V Substitution - Missense 16:68811714-68811714 + PD18049a COSM5752802 c.1885_1886insA p.L630fs*33 Insertion - Frameshift 16:68822174-68822175 + TCGA-EE-A20H-06 COSM3532331 c.39C>T p.I13I Substitution - coding silent 19:3523028-3523028 + TCGA-D7-A4YU-01 COSM4062174 c.476C>T p.P159L Substitution - Missense 16:68808512-68808512 + TCGA-A2-A0T4-01 COSM435609 c.2267_2268insT p.E757fs*1 Insertion - Frameshift 16:68828276-68828277 + TCGA-OL-A5DA-01 COSM5833141 c.539delC p.N181fs*34 Deletion - Frameshift 16:68808700-68808700 + TCGA-CC-5260-01 COSM435605 c.1936+1G>A p.? Unknown 16:68822226-68822226 + CSB30 COSM5028161 c.1520delC p.Y508fs*14 Deletion - Frameshift 16:68815714-68815714 + TCGA-DK-A1AG-01 COSM1302178 c.1156G>A p.E386K Substitution - Missense 16:68813331-68813331 + TCGA-D7-6518-01 COSM4062180 c.869A>G p.D290G Substitution - Missense 16:68811720-68811720 + CSCC-31-T COSM4480079 c.2386C>T p.R796W Substitution - Missense 16:68829744-68829744 + BD236T COSM5519579 c.541G>A p.A181T Substitution - Missense 19:3527701-3527701 + TCGA-AC-A3OD-01 COSM3818354 c.1921C>T p.Q641* Substitution - Nonsense 16:68822210-68822210 + CSCC-35-T COSM4467617 c.149C>T p.P50L Substitution - Missense 19:3525947-3525947 + PT48 COSM5933424 c.1162G>A p.E388K Substitution - Missense 16:68813337-68813337 + TCGA-GC-A3I6-01 COSM1302179 c.2392C>G p.L798V Substitution - Missense 16:68829750-68829750 + 1001715 COSM20828 c.1009-3_1009-1delCAG p.? Unknown 16:68812132-68812134 + H292 COSM19743 c.1849G>A p.A617T Substitution - Missense 16:68822138-68822138 + TCGA-E2-A2P6-01 COSM5833143 c.612_613insT p.I206fs*3 Insertion - Frameshift 16:68808773-68808774 + SK-BR-5 COSM19826 c.532-1G>C p.? Unknown 16:68808692-68808692 + YUDON COSM5389373 c.1088G>A p.W363* Substitution - Nonsense 19:3532496-3532496 + PR-05-3440 COSM243589 c.767A>T p.N256I Substitution - Missense 16:68810276-68810276 + 997046 COSM19763 c.1627delT p.S543fs*14 Deletion - Frameshift 16:68819341-68819341 + 1001687 COSM20826 c.? p.S337_T379del Deletion - In frame TCGA-BH-A0HP-01 COSM435590 c.688-1G>A p.? Unknown 16:68810196-68810196 + 996989 COSM19761 c.1196_1199delCTGA p.T399fs*17 Deletion - Frameshift 16:68813371-68813374 + 19M COSM5578606 c.439C>T p.P147S Substitution - Missense 19:3527031-3527031 + ESO-119 COSM1247779 c.1596G>A p.W532* Substitution - Nonsense 16:68819310-68819310 + PD11358a COSM5752529 c.832+1G>C p.? Unknown 16:68810342-68810342 + SW48 COSM4336502 c.487_488insC p.R165fs*60 Insertion - Frameshift 19:3527647-3527648 + TCGA-C4-A0F0-01 COSM417306 c.398C>T p.S133F Substitution - Missense 16:68808434-68808434 + LC160 COSM1302174 c.337A>G p.K113E Substitution - Missense 16:68801843-68801843 + TCGA-A8-A09Z-01 COSM20785 c.371_372insC p.P127fs*41 Insertion - Frameshift 16:68801877-68801878 + 587316 COSM1207722 c.938G>A p.R313Q Substitution - Missense 19:3532025-3532025 + pfg122T COSM4756930 c.2557T>C p.S853P Substitution - Missense 16:68833407-68833407 + PD5960a COSM5752675 c.2164+1G>T p.? Unknown 16:68823627-68823627 + 997762 COSM19798 c.1207_1208insC p.N405fs*14 Insertion - Frameshift 16:68813382-68813383 + YURAY COSM5389371 c.682G>A p.E228K Substitution - Missense 19:3530819-3530819 + 996993 COSM19762 c.1510G>T p.E504* Substitution - Nonsense 16:68815704-68815704 + TCGA-DD-A116-01 COSM4912266 c.575T>G p.L192R Substitution - Missense 19:3527735-3527735 + TCGA-GM-A5PX-01 COSM5833145 c.909_910insA p.I304fs*7 Insertion - Frameshift 16:68811760-68811761 + TCGA-B5-A11E-01 COSM972802 c.2280C>T p.G760G Substitution - coding silent 16:68828289-68828289 + TCGA-EK-A2RN-01 COSM4823144 c.313G>A p.E105K Substitution - Missense 19:3526312-3526312 + TCGA-G4-6586-01 COSM19494 c.372delC p.P126fs*89 Deletion - Frameshift 16:68801878-68801878 + TCGA-FP-8210-01 COSM19782 c.770A>G p.D257G Substitution - Missense 16:68810279-68810279 + 999880 COSM19751 c.1027delC p.L343fs*13 Deletion - Frameshift 16:68812153-68812153 + 2542198 COSM5945837 c.? p.T379M Substitution - Missense 2530678 COSM3197037 c.464A>G p.N155S Substitution - Missense 19:3527056-3527056 + TCGA-06-0210-02 COSM19822 c.1901C>T p.A634V Substitution - Missense 16:68822190-68822190 + T3610 COSM4686006 c.253G>A p.G85S Substitution - Missense 19:3526177-3526177 + TCGA-JW-A5VL-01 COSM4846766 c.957C>G p.L319L Substitution - coding silent 19:3532044-3532044 + YUGOE COSM1711607 c.263G>A p.G88D Substitution - Missense 19:3526262-3526262 + TCGA-GM-A3XN-01 COSM5833139 c.190_191insA p.R65fs*29 Insertion - Frameshift 16:68801696-68801697 + TCGA-A8-A09W-01 COSM435605 c.1936+1G>A p.? Unknown 16:68822226-68822226 + PTC-14C COSM4129241 c.1223C>A p.A408E Substitution - Missense 16:68813398-68813398 + 1530130 COSM19758 c.1774G>A p.A592T Substitution - Missense 16:68822063-68822063 + pfg122T COSM4765272 c.357_358insG p.H121fs*47 Insertion - Frameshift 16:68801863-68801864 + PCSI_0085_Pa_P_526 COSM4961715 c.387+10C>T p.? Unknown 19:3526396-3526396 + PD3849a COSM165997 c.846delG p.E283fs*11 Deletion - Frameshift 16:68811697-68811697 + KYSE-510 COSM2996772 c.1280C>A p.T427K Substitution - Missense 16:68813455-68813455 + PD4110a COSM165998 c.2275delG p.G759fs*11 Deletion - Frameshift 16:68828284-68828284 + TCGA-AZ-6605-01 COSM1379192 c.2185C>T p.L729L Substitution - coding silent 16:68828194-68828194 + MDA-MB-134IV COSM19830 c.?_?del? p.? Unknown HCC2998 COSM1679222 c.665G>T p.R222I Substitution - Missense 16:68808826-68808826 + TCGA-A7-A4SC-01 COSM5833144 c.863_864delAC p.D288fs*4 Deletion - Frameshift 16:68811714-68811715 + TCGA-E2-A1IJ-01 COSM1479035 c.2032_2033insT p.T679fs*9 Insertion - Frameshift 16:68823494-68823495 + 25 COSM19750 c.1204G>A p.D402N Substitution - Missense 16:68813379-68813379 + PD7209a COSM5752413 c.2453_2463del11 p.D819fs*6 Deletion - Frameshift 16:68833303-68833313 + CAL33 COSM4593023 c.947T>G p.V316G Substitution - Missense 19:3532034-3532034 + CHC1704T COSM4804144 c.407G>T p.R136L Substitution - Missense 19:3526999-3526999 + TCGA-AR-A2LE-01 COSM19780 c.763C>T p.Q255* Substitution - Nonsense 16:68810272-68810272 + TCGA-C8-A3M7-01 COSM5833146 c.1019_1020insG p.Y341fs*9 Insertion - Frameshift 16:68812145-68812146 + 999882 COSM19753 c.1009-1G>A p.? Unknown 16:68812134-68812134 + 92T COSM5576296 c.663_671delTAGAGAACG p.R222_R224delRER Deletion - In frame 16:68808824-68808832 + SUM44PE COSM19827 c.1269delT p.F423fs*8 Deletion - Frameshift 16:68813444-68813444 + BT857 COSM19538 c.1971delC p.L658fs*1 Deletion - Frameshift 16:68823433-68823433 + LIM2551 COSM4644008 c.2617G>A p.A873T Substitution - Missense 16:68833467-68833467 + Au4 COSM5578607 c.439C>T p.P147S Substitution - Missense 19:3527031-3527031 + SNUH_G52_S1 COSM3999899 c.633A>T p.T211T Substitution - coding silent 16:68808794-68808794 + 2521337 COSM19821 c.1018A>G p.T340A Substitution - Missense 16:68812144-68812144 + TCGA-AR-A24X-01 COSM1479036 c.2165-1G>T p.? Unknown 16:68828173-68828173 + 210T COSM4062178 c.664A>G p.R222G Substitution - Missense 16:68808825-68808825 + 178T COSM4062177 c.569A>G p.Y190C Substitution - Missense 16:68808730-68808730 + 1988999 COSM19743 c.1849G>A p.A617T Substitution - Missense 16:68822138-68822138 + 996870 COSM19751 c.1027delC p.L343fs*13 Deletion - Frameshift 16:68812153-68812153 + 2492710 COSM5718455 c.855G>T p.S285S Substitution - coding silent 19:3531942-3531942 + 997117 COSM19771 c.1107C>T p.N369N Substitution - coding silent 16:68812233-68812233 + 999865 COSM20772 c.1093G>C p.V365L Substitution - Missense 16:68812219-68812219 + TCGA-E2-A107-01 COSM20795 c.1008G>A p.E336E Substitution - coding silent 16:68811859-68811859 + 999858 COSM19753 c.1009-1G>A p.? Unknown 16:68812134-68812134 + 997335 COSM19834 c.? p.?A>V Substitution - Missense CHC1704T COSM4804143 c.407G>T p.R136L Substitution - Missense 19:3526999-3526999 + PD7238a COSM5801043 c.494_495insA p.N166fs*2 Insertion - Frameshift 16:68808530-68808531 + 997119 COSM19775 c.925C>T p.P309S Substitution - Missense 16:68811776-68811776 + pfg317T COSM4747424 c.796_810del15 p.F267_V271delFKGSV Deletion - In frame 16:68810305-68810319 + SJDES011-R COSM4579194 c.1277_1278CC>AA p.T426K Substitution - Missense 16:68813452-68813453 + 997322 COSM19776 c.922G>A p.D308N Substitution - Missense 16:68811773-68811773 + BCM723T COSM5348163 c.1124delG p.G375fs*14 Deletion - Frameshift 19:3532532-3532532 + NCI-H2087 COSM22062 c.758T>C p.V253A Substitution - Missense 19:3531751-3531751 + TCGA-AX-A0J0-01 COSM972790 c.1671G>T p.K557N Substitution - Missense 16:68819385-68819385 + 996891 COSM19757 c.1320+?del? p.? Unknown 2497773 COSM4756924 c.539C>T p.S180F Substitution - Missense 16:68808700-68808700 + TCGA-A2-A0CO-01 COSM194600 c.1003C>T p.R335* Substitution - Nonsense 16:68811854-68811854 + BCT-B-H12 COSM19499 c.2440-1G>C p.? Unknown 16:68833289-68833289 + XHDG25 COSM4593024 c.947T>G p.V316G Substitution - Missense 19:3532034-3532034 + 997326 COSM19784 c.786_794delCACCCAGGA p.F262_E265>L Complex - deletion inframe 16:68810295-68810303 + TCGA-BS-A0U8-01 COSM972804 c.2471C>T p.A824V Substitution - Missense 16:68833321-68833321 + TCGA-F1-6874-01 COSM4062184 c.1320G>T p.K440N Substitution - Missense 16:68813495-68813495 + PD14472a COSM5801711 c.75_76insG p.E26fs*8 Insertion - Frameshift 16:68738323-68738324 + PD4203a COSM159883 c.1480G>T p.E494* Substitution - Nonsense 16:68815674-68815674 + 15812 COSM5029231 c.1990delA p.I665fs*14 Deletion - Frameshift 16:68823452-68823452 + TCGA-BR-4292-01 COSM4062173 c.304G>A p.A102T Substitution - Missense 16:68801810-68801810 + TCGA-A8-A09T-01 COSM20785 c.371_372insC p.P127fs*41 Insertion - Frameshift 16:68801877-68801878 + 2233656 COSM4172531 c.? p.K520E Substitution - Missense pfg094T COSM4062176 c.563T>A p.V188D Substitution - Missense 16:68808724-68808724 + PD9578a COSM5752496 c.163+1_163+2delGT p.? Unknown 16:68738412-68738413 + TCGA-G3-A7M8-01 COSM4922542 c.1048C>T p.Q350* Substitution - Nonsense 19:3532456-3532456 + CHC892T COSM2996768 c.1138-1G>A p.? Unknown 16:68813312-68813312 + CHC892T COSM2996768 c.1138-1G>A p.? Unknown 16:68813312-68813312 + TCGA-EE-A2GR-06 COSM3511250 c.210C>T p.S70S Substitution - coding silent 16:68801716-68801716 + 996696 COSM19742 c.2131C>G p.L711V Substitution - Missense 16:68823593-68823593 + TCGA-E1-5303-01 COSM3970910 c.1126G>C p.G376R Substitution - Missense 19:3532534-3532534 + TCGA-A1-A0SE-01 COSM435592 c.727G>A p.E243K Substitution - Missense 16:68810236-68810236 + 1992435 COSM1666631 c.? p.G577fs*7 Unknown SJDES011-R COSM4579195 c.1278C>A p.T426T Substitution - coding silent 16:68813453-68813453 + CSCC-55-T COSM4530917 c.173G>A p.S58N Substitution - Missense 19:3525971-3525971 + SCC-15 COSM308522 c.1214A>G p.N405S Substitution - Missense 16:68813389-68813389 + 999877 COSM19747 c.1057G>T p.E353* Substitution - Nonsense 16:68812183-68812183 + TCGA-E2-A10F-01 COSM435596 c.931_932insT p.D313fs*1 Insertion - Frameshift 16:68811782-68811783 + 5 COSM1659145 c.499G>T p.E167* Substitution - Nonsense 16:68808535-68808535 + 999860 COSM20771 c.1198G>T p.D400Y Substitution - Missense 16:68813373-68813373 + BT823 COSM19524 c.? p.Q346* Substitution - Nonsense B34-Tumor COSM1749722 c.1914G>A p.W638* Substitution - Nonsense 16:68822203-68822203 + BT853 COSM19525 c.248_249ins41 p.T84fs*47 Insertion - Frameshift 16:68801754-68801755 + KM12 COSM4281460 c.90C>T p.T30T Substitution - coding silent 19:3525888-3525888 + UACC-893 COSM35880 c.699C>G p.H233Q Substitution - Missense 16:68810208-68810208 + CRC-06T COSM5457513 c.1807_1808insTG p.C603fs*11 Insertion - Frameshift 16:68822096-68822097 + KYSE510 COSM2996772 c.1280C>A p.T427K Substitution - Missense 16:68813455-68813455 + 9 COSM1659139 c.2155_2156insG p.A719fs*29 Insertion - Frameshift 16:68823617-68823618 + S04-45633-TP COSM4990895 c.1874C>T p.P625L Substitution - Missense 16:68822163-68822163 + MKN45 COSM20824 c.823_832+8del18 p.? Unknown 16:68810332-68810349 + TCGA-CA-6717-01 COSM1379141 c.394G>A p.V132I Substitution - Missense 16:68808430-68808430 + TCGA-42-2590-01 COSM1324346 c.662A>T p.D221V Substitution - Missense 16:68808823-68808823 + P-Thy037 COSM5095517 c.2431A>G p.I811V Substitution - Missense 16:68829789-68829789 + pfg136T COSM4756921 c.469G>C p.V157L Substitution - Missense 16:68808505-68808505 + TCGA-D7-6522-01 COSM20830 c.1320+1G>T p.? Unknown 16:68813496-68813496 + ESO-049 COSM1247778 c.1489G>A p.E497K Substitution - Missense 16:68815683-68815683 + T2944 COSM4686008 c.662G>A p.R221Q Substitution - Missense 19:3530799-3530799 + PD14460a COSM5752137 c.110_112ACA>G p.Y37fs*21 Complex - frameshift 16:68738358-68738360 + 2215759 COSM4169305 c.? p.Q351fs*3 Unknown SH-1362 COSM5019357 c.2440-6C>G p.? Unknown 16:68833284-68833284 + CAMA-1 COSM19824 c.1712-1G>A p.? Unknown 16:68822000-68822000 + 993005 COSM19517 c.989C>T p.T330I Substitution - Missense 16:68811840-68811840 + TCGA-A8-A0A4-01 COSM435610 c.2291_2292insC p.Q765fs*4 Insertion - Frameshift 16:68828300-68828301 + PD2127a COSM51899 c.1201C>T p.Q401* Substitution - Nonsense 19:3532609-3532609 + SH-8559 COSM20775 c.2253C>T p.N751N Substitution - coding silent 16:68828262-68828262 + TCGA-JW-A5VL-01 COSM4846767 c.957C>G p.L319L Substitution - coding silent 19:3532044-3532044 + TCGA-D8-A27T-01 COSM1479024 c.1137G>A p.T379T Substitution - coding silent 16:68812263-68812263 + TCGA-FW-A3R5-06 COSM3888814 c.601C>T p.P201S Substitution - Missense 16:68808762-68808762 + 996867 COSM19747 c.1057G>T p.E353* Substitution - Nonsense 16:68812183-68812183 + 1530112 COSM96852 c.96_97insA p.D33fs*26 Insertion - Frameshift 16:68738344-68738345 + 1 COSM5731892 c.1336G>T p.A446S Substitution - Missense 16:68815530-68815530 + pfg143T COSM4336503 c.1119delG p.G375fs*14 Deletion - Frameshift 19:3532527-3532527 + TCGA-BH-A18P-01 COSM435584 c.106delA p.S36fs*20 Deletion - Frameshift 16:68738354-68738354 + TCGA-A2-A25A-01 COSM972800 c.2195G>A p.R732Q Substitution - Missense 16:68828204-68828204 + TCGA-B5-A11F-01 COSM972800 c.2195G>A p.R732Q Substitution - Missense 16:68828204-68828204 + TCGA-A8-A091-01 COSM435592 c.727G>A p.E243K Substitution - Missense 16:68810236-68810236 + PD9067a COSM5752870 c.78_79insC p.C28fs*6 Insertion - Frameshift 16:68738326-68738327 + MPE600 COSM20796 c.1138_1320del183 p.Y380_K440del61 Deletion - In frame 16:68813313-68813495 + MDA-MB-134-VI COSM35882 c.688_832del145 p.L230fs*4 Deletion - Frameshift 16:68810197-68810341 + TCGA-A8-A0AB-01 COSM435599 c.1200_1201insA p.A401fs*2 Insertion - Frameshift 16:68813375-68813376 + TCGA-DG-A2KL-01 COSM4851351 c.1135G>C p.D379H Substitution - Missense 19:3532543-3532543 + 826 COSM5029278 c.1267delT p.F423fs*8 Deletion - Frameshift 16:68813442-68813442 + TCGA-EE-A2MR-06 COSM3532359 c.528C>T p.F176F Substitution - coding silent 19:3527688-3527688 + 993003 COSM19515 c.1309_1310delAA p.K437fs*8 Deletion - Frameshift 16:68813484-68813485 + ESCC-F120 COSM5047122 c.1759G>C p.D587H Substitution - Missense 16:68822048-68822048 + 1318 COSM19487 c.22_43del22 p.L8fs*41 Deletion - Frameshift 16:68737437-68737458 + 587224 COSM1180831 c.2321delG p.G775fs*8 Deletion - Frameshift 16:68829679-68829679 + TCGA-GN-A262-06 COSM3532362 c.648C>T p.T216T Substitution - coding silent 19:3527808-3527808 + PD13306a COSM5752199 c.410delC p.A137fs*78 Deletion - Frameshift 16:68808446-68808446 + TCGA-BH-A28Q-01 COSM20785 c.371_372insC p.P127fs*41 Insertion - Frameshift 16:68801877-68801878 + DM10 COSM5608064 c.1980G>T p.V660V Substitution - coding silent 16:68823442-68823442 + PD4194a COSM219704 c.86_89ACCC>GTG p.H29fs*27 Complex - frameshift 16:68738334-68738337 + S02194 COSM5674840 c.211C>G p.P71A Substitution - Missense 19:3526135-3526135 + MO_1012 COSM5547168 c.1952delT p.L652fs*1 Deletion - Frameshift 16:68823414-68823414 + TCGA-B9-A69E-01 COSM3988618 c.1566A>C p.T522T Substitution - coding silent 16:68819280-68819280 + TCGA-F4-6856-01 COSM19494 c.372delC p.P126fs*89 Deletion - Frameshift 16:68801878-68801878 + PD9423a COSM1609556 c.1161C>T p.N387N Substitution - coding silent 16:68813336-68813336 + 2148484 COSM2996743 c.287T>C p.I96T Substitution - Missense 16:68801793-68801793 + TCGA-B6-A0IP-01 COSM435591 c.692_693delTC p.H233fs*10 Deletion - Frameshift 16:68810201-68810202 + CAL27 COSM4593023 c.947T>G p.V316G Substitution - Missense 19:3532034-3532034 + 17740 COSM5029222 c.791_801del11 p.E265fs*24 Deletion - Frameshift 16:68810300-68810310 + PD4126a COSM166000 c.338_348del11 p.V114fs*50 Deletion - Frameshift 16:68801844-68801854 + 1855647 COSM1169612 c.1105_1106insACCAAC p.N369_D370insQH Insertion - In frame 16:68812231-68812232 + MaPT02 COSM5731107 c.2233G>T p.E745* Substitution - Nonsense 16:68828242-68828242 + 2521336 COSM19821 c.1018A>G p.T340A Substitution - Missense 16:68812144-68812144 + PD14460a COSM5795622 c.112A>G p.T38A Substitution - Missense 16:68738360-68738360 + T1232 COSM4686012 c.1333C>T p.R445C Substitution - Missense 19:3533384-3533384 + 70 COSM20789 c.2222_2223insA p.L742fs*6 Insertion - Frameshift 16:68828231-68828232 + HCC25 COSM1612053 c.670G>A p.D224N Substitution - Missense 19:3530807-3530807 + CRC-26T COSM5482790 c.1480A>C p.R494R Substitution - coding silent 19:3534825-3534825 + Au4 COSM5578606 c.439C>T p.P147S Substitution - Missense 19:3527031-3527031 + 2492710 COSM5718456 c.855G>T p.S285S Substitution - coding silent 19:3531942-3531942 + CHC2352T COSM4943137 c.2615T>A p.L872Q Substitution - Missense 16:68833465-68833465 + WSU-HN8 COSM4593024 c.947T>G p.V316G Substitution - Missense 19:3532034-3532034 + pfg016T COSM1640537 c.2080G>A p.V694I Substitution - Missense 16:68823542-68823542 + YUAKER COSM1709328 c.269_270GG>AA p.R90Q Substitution - Missense 16:68801775-68801776 + BCT107 COSM19498 c.866_867delCG p.A289fs*3 Deletion - Frameshift 16:68811717-68811718 + TCGA-B5-A11E-01 COSM994814 c.84G>A p.R28R Substitution - coding silent 19:3525882-3525882 + T2944 COSM4686011 c.1161G>A p.T387T Substitution - coding silent 19:3532569-3532569 + 2492721 COSM5722785 c.699C>T p.T233T Substitution - coding silent 19:3530836-3530836 + 1855646 COSM1169613 c.1320+5G>A p.? Unknown 16:68813500-68813500 + 17352 COSM4613899 c.1472_1473delAG p.R492fs*44 Deletion - Frameshift 16:68815666-68815667 + TCGA-D8-A27V-01 COSM19503 c.67C>T p.Q23* Substitution - Nonsense 16:68738315-68738315 + PTC-7C COSM5446458 c.2612_2613insT p.K871fs*4 Insertion - Frameshift 16:68833462-68833463 + TCGA-AC-A3YI-01 COSM5833156 c.2288_2289insG p.D764fs*5 Insertion - Frameshift 16:68828297-68828298 + BCT101 COSM19495 c.378_379insC p.H128fs*40 Insertion - Frameshift 16:68801884-68801885 + 1001719 COSM19502 c.59G>A p.W20* Substitution - Nonsense 16:68738307-68738307 + XHDG07C COSM4770170 c.1417delT p.F473fs*>21 Deletion - Frameshift 19:3534490-3534490 + TCGA-32-1982-01 COSM3402438 c.1773C>T p.N591N Substitution - coding silent 16:68822062-68822062 + BT154 COSM19523 c.? p.R335* Substitution - Nonsense TCGA-A7-A13H-01 COSM5029219 c.288delC p.H97fs*20 Deletion - Frameshift 16:68801794-68801794 + TCGA-CG-4437-01 COSM4076890 c.171G>C p.W57C Substitution - Missense 19:3525969-3525969 + 992723 COSM19485 c.944A>G p.N315S Substitution - Missense 16:68811795-68811795 + pfg334T COSM4756928 c.1355T>G p.L452R Substitution - Missense 16:68815549-68815549 + 17327 COSM5029233 c.2262delC p.Y755fs*15 Deletion - Frameshift 16:68828271-68828271 + CSCC-15-T COSM4467438 c.148C>T p.P50S Substitution - Missense 19:3525946-3525946 + T3174 COSM4670764 c.700G>A p.A234T Substitution - Missense 16:68810209-68810209 + BT995A COSM19531 c.1224delG p.W409fs*8 Deletion - Frameshift 16:68813399-68813399 + TCGA-D8-A27G-01 COSM5226337 c.499_500insA p.G169fs*5 Insertion - Frameshift 16:68808535-68808536 + TCGA-EE-A2MR-06 COSM3532356 c.393C>T p.S131S Substitution - coding silent 19:3526985-3526985 + SH-3776 COSM5020068 c.1680G>C p.T560T Substitution - coding silent 16:68819394-68819394 + 996870 COSM19750 c.1204G>A p.D402N Substitution - Missense 16:68813379-68813379 + MDA-MB-453 COSM19418 c.1913G>A p.W638* Substitution - Nonsense 16:68822202-68822202 + LS411 COSM4281473 c.426C>T p.G142G Substitution - coding silent 19:3527018-3527018 + 2280422 COSM4381092 c.? p.P159_F171>L Complex - deletion inframe TCGA-ER-A19E-06 COSM3532354 c.148C>T p.P50S Substitution - Missense 19:3525946-3525946 + SA210 COSM213835 c.583C>A p.Q195K Substitution - Missense 16:68808744-68808744 + SNU-C2B COSM19494 c.372delC p.P126fs*89 Deletion - Frameshift 16:68801878-68801878 + pfg156T COSM19516 c.760G>T p.D254Y Substitution - Missense 16:68810269-68810269 + PD11740a COSM19759 c.781G>T p.E261* Substitution - Nonsense 16:68810290-68810290 + HCT116 COSM4281469 c.209C>T p.S70F Substitution - Missense 19:3526133-3526133 + PCSI_0083_Pa_X COSM1379173 c.1199A>G p.D400G Substitution - Missense 16:68813374-68813374 + 997324 COSM19777 c.2218C>T p.P740S Substitution - Missense 16:68828227-68828227 + TCGA-A2-A0CR-01 COSM435585 c.187C>T p.R63* Substitution - Nonsense 16:68801693-68801693 + TCGA-A2-A0SY-01 COSM435583 c.52_53insCA p.S19fs*38 Insertion - Frameshift 16:68738300-68738301 + GB16 COSM1742969 c.1118C>G p.P373R Substitution - Missense 16:68812244-68812244 + 19M COSM5578607 c.439C>T p.P147S Substitution - Missense 19:3527031-3527031 + I2L-P19Ta-Tumor-Biopsy COSM5364938 c.1294T>G p.S432A Substitution - Missense 19:3533345-3533345 + pfg345T COSM19822 c.1901C>T p.A634V Substitution - Missense 16:68822190-68822190 + TCGA-AG-3892-01 COSM256583 c.1942G>T p.E648* Substitution - Nonsense 16:68823404-68823404 + TCGA-BR-6803-01 COSM19516 c.760G>T p.D254Y Substitution - Missense 16:68810269-68810269 + SC-her2-036 COSM4777511 c.192_193AA>TT p.Q64_R65>HW Complex - compound substitution 16:68801698-68801699 + SK-BR-5 COSM19826 c.532-1G>C p.? Unknown 16:68808692-68808692 + TCGA-DD-A116-01 COSM4912267 c.575T>G p.L192R Substitution - Missense 19:3527735-3527735 + YURAY COSM5389372 c.682G>A p.E228K Substitution - Missense 19:3530819-3530819 + 1618320 COSM143802 c.1223C>T p.A408V Substitution - Missense 16:68813398-68813398 + LP2000108-DNA_A01 COSM4062180 c.869A>G p.D290G Substitution - Missense 16:68811720-68811720 + LUAD-B01811 COSM334040 c.194_195GG>TT p.R65I Substitution - Missense 16:68801700-68801701 + 997330 COSM19506 c.856G>A p.A286T Substitution - Missense 16:68811707-68811707 + 56580 COSM1583006 c.590C>T p.S197F Substitution - Missense 19:3527750-3527750 + TCGA-A8-A07B-01 COSM3818344 c.601C>G p.P201A Substitution - Missense 16:68808762-68808762 + 1001713 COSM20826 c.? p.S337_T379del Deletion - In frame S01516 COSM5669042 c.127C>T p.R43W Substitution - Missense 16:68738375-68738375 + 5 COSM19785 c.786_794CACCCAGGA>T p.T263fs*3 Complex - frameshift 16:68810295-68810303 + TCGA-G2-A3IE-01 COSM1302177 c.937G>A p.D313N Substitution - Missense 16:68811788-68811788 + TCGA-GI-A2C8-01 COSM1479025 c.1226G>T p.W409L Substitution - Missense 16:68813401-68813401 + CHC465T COSM3668242 c.1450T>A p.S484T Substitution - Missense 19:3534804-3534804 + D-03 COSM4766187 c.531+2T>C p.? Unknown 16:68808569-68808569 + 61 COSM5741347 c.607G>A p.V203M Substitution - Missense 19:3527767-3527767 + 996865 COSM19753 c.1009-1G>A p.? Unknown 16:68812134-68812134 + PD9589a COSM5752498 c.1858delC p.P620fs*11 Deletion - Frameshift 16:68822147-68822147 + PD11358a COSM5752529 c.832+1G>C p.? Unknown 16:68810342-68810342 + EOPC-03_tumor COSM2996759 c.817G>A p.E273K Substitution - Missense 16:68810326-68810326 + TCGA-DD-A3A8-01 COSM4934916 c.855A>G p.T285T Substitution - coding silent 16:68811706-68811706 + 17972 COSM5029228 c.1863_1864insAATA p.T623fs*41 Insertion - Frameshift 16:68822152-68822153 + 1001698 COSM20779 c.?_?del? p.? Unknown YUDON COSM5389374 c.1088G>A p.W363* Substitution - Nonsense 19:3532496-3532496 + PCSI_0105_Pa_P_526 COSM4962211 c.802G>C p.E268Q Substitution - Missense 19:3531795-3531795 + 1001684 COSM20776 c.1109A>C p.D370A Substitution - Missense 16:68812235-68812235 + TCGA-AO-A0J8-01 COSM435607 c.2120delT p.P708fs*14 Deletion - Frameshift 16:68823582-68823582 + TCGA-BP-4976-01 COSM474555 c.1281C>A p.V427V Substitution - coding silent 19:3533332-3533332 + 3 COSM1659129 c.1009-2_1029del23 p.? Unknown 16:68812133-68812155 + CSB31 COSM5028158 c.922_935del14 p.D308fs*1 Deletion - Frameshift 16:68811773-68811786 + PD9755a COSM5782708 c.832+3A>G p.? Unknown 16:68810344-68810344 + 997050 COSM19767 c.1795_1796AC>T p.T599fs*14 Complex - frameshift 16:68822084-68822085 + DGC1 COSM19822 c.1901C>T p.A634V Substitution - Missense 16:68822190-68822190 + BHY COSM4593023 c.947T>G p.V316G Substitution - Missense 19:3532034-3532034 + 806 COSM19490 c.1529_1533delCCCAG p.A510fs*25 Deletion - Frameshift 16:68815723-68815727 + 1001728 COSM20839 c.1387G>C p.E463Q Substitution - Missense 16:68815581-68815581 + BT992 COSM19533 c.1564_1565insGT p.T522fs*36 Insertion - Frameshift 16:68815758-68815759 + 1179080 COSM28934 c.240_241insGGTG p.V82fs*13 Insertion - Frameshift 16:68801746-68801747 + 17946 COSM5029226 c.1567_1568insA p.Y523fs*1 Insertion - Frameshift 16:68819281-68819282 + TCGA-CJ-4895-01 COSM1392389 c.757G>A p.V253M Substitution - Missense 19:3531750-3531750 + PD4985a COSM19780 c.763C>T p.Q255* Substitution - Nonsense 16:68810272-68810272 + EGC15 COSM5055033 c.1744_1746delCTG p.L583delL Deletion - In frame 16:68822033-68822035 + MT-439-T2 COSM5651599 c.954C>A p.T318T Substitution - coding silent 16:68811805-68811805 + TCGA-E2-A1IH-01 COSM1479029 c.1819C>T p.P607S Substitution - Missense 16:68822108-68822108 + GC_350T-GC_350N COSM2996774 c.1320+1G>A p.? Unknown 16:68813496-68813496 + YUKLAB COSM1709330 c.2022T>A p.N674K Substitution - Missense 16:68823484-68823484 + 587228 COSM972800 c.2195G>A p.R732Q Substitution - Missense 16:68828204-68828204 + TCGA-D5-6931-01 COSM3755010 c.2076T>C p.A692A Substitution - coding silent 16:68823538-68823538 + TCGA-B6-A40C-01 COSM19503 c.67C>T p.Q23* Substitution - Nonsense 16:68738315-68738315 + TCGA-AD-6964-01 COSM1379144 c.714C>T p.N238N Substitution - coding silent 16:68810223-68810223 + BN24T COSM1609556 c.1161C>T p.N387N Substitution - coding silent 16:68813336-68813336 + TCGA-CG-4441-01 COSM4076893 c.1251G>T p.T417T Substitution - coding silent 19:3533302-3533302 + BT572 COSM19530 c.? p.? Unknown TCGA-CW-6093-01 COSM474552 c.48G>C p.Q16H Substitution - Missense 19:3523037-3523037 + TCGA-BH-A18F-01 COSM435604 c.1743_1744insCTGC p.L583fs*6 Insertion - Frameshift 16:68822032-68822033 + TCGA-AC-A2FG-01 COSM5205432 c.597_598insC p.V202fs*7 Insertion - Frameshift 16:68808758-68808759 + T2944 COSM4686009 c.662G>A p.R221Q Substitution - Missense 19:3530799-3530799 + BICR_22 COSM4593024 c.947T>G p.V316G Substitution - Missense 19:3532034-3532034 + PD11376a COSM5752535 c.388-1G>C p.? Unknown 16:68808423-68808423 + 43T COSM5055032 c.641T>C p.L214P Substitution - Missense 16:68808802-68808802 + 16296 COSM5029235 c.2439+2T>G p.? Unknown 16:68829799-68829799 + DN14066 COSM19503 c.67C>T p.Q23* Substitution - Nonsense 16:68738315-68738315 + BT454 COSM19530 c.? p.? Unknown TCGA-AP-A0LM-01 COSM972776 c.294C>A p.F98L Substitution - Missense 16:68801800-68801800 + TCGA-CG-5733-01 COSM4062186 c.2205G>A p.A735A Substitution - coding silent 16:68828214-68828214 + 12 COSM19786 c.779C>T p.P260L Substitution - Missense 16:68810288-68810288 + pfg402T COSM972800 c.2195G>A p.R732Q Substitution - Missense 16:68828204-68828204 + TCGA-A2-A4S2-01 COSM3818356 c.2505T>A p.Y835* Substitution - Nonsense 16:68833355-68833355 + TCGA-FD-A3N5-01 COSM1304426 c.1429C>T p.R477C Substitution - Missense 19:3534502-3534502 + 180T COSM20774 c.1418T>A p.V473D Substitution - Missense 16:68815612-68815612 + CHC2352T COSM4943137 c.2615T>A p.L872Q Substitution - Missense 16:68833465-68833465 + PD8618a COSM5752695 c.2295+5G>T p.? Unknown 16:68828309-68828309 + TCGA-A7-A3J1-01 COSM5833151 c.2131delC p.L711fs*11 Deletion - Frameshift 16:68823593-68823593 + PD5936a COSM5801028 c.1208_1209insC p.N405fs*14 Insertion - Frameshift 16:68813383-68813384 + UM-SCC-2 COSM4593023 c.947T>G p.V316G Substitution - Missense 19:3532034-3532034 + TCGA-AP-A059-01 COSM994820 c.1293C>A p.P431P Substitution - coding silent 19:3533344-3533344 + SNU-C2B COSM3197045 c.1084G>A p.A362T Substitution - Missense 19:3532492-3532492 + PT36 COSM5916496 c.710C>T p.S237F Substitution - Missense 16:68810219-68810219 + 2443925 COSM5414678 c.2289_?del(7236) p.? Unknown PD9597a COSM19780 c.763C>T p.Q255* Substitution - Nonsense 16:68810272-68810272 + PD6466b COSM5772201 c.2164+3A>C p.? Unknown 16:68823629-68823629 + 2557_PT COSM20839 c.1387G>C p.E463Q Substitution - Missense 16:68815581-68815581 + T2941 COSM1379139 c.221G>A p.R74Q Substitution - Missense 16:68801727-68801727 + 1001693 COSM20827 c.? p.Y380_K440del Deletion - In frame 12 COSM1659129 c.1009-2_1029del23 p.? Unknown 16:68812133-68812155 + S05-31806-TP COSM4990899 c.2554G>A p.E852K Substitution - Missense 16:68833404-68833404 + YUZINO COSM1709329 c.739G>A p.E247K Substitution - Missense 16:68810248-68810248 + PD6782a COSM19798 c.1207_1208insC p.N405fs*14 Insertion - Frameshift 16:68813382-68813383 + TCGA-AP-A056-01 COSM972786 c.781G>A p.E261K Substitution - Missense 16:68810290-68810290 + BT392 COSM19541 c.1009-2_1009-1delAG p.? Unknown 16:68812133-68812134 + TCGA-D3-A3ML-06 COSM3532360 c.587C>T p.S196L Substitution - Missense 19:3527747-3527747 + PD18188a COSM5752138 c.971_978GAGTCATC>T p.G324fs*30 Complex - frameshift 16:68811822-68811829 + 2012-1351:2012-338-T COSM19499 c.2440-1G>C p.? Unknown 16:68833289-68833289 + I2L-P19Ta-Tumor-Biopsy COSM5364939 c.1294T>G p.S432A Substitution - Missense 19:3533345-3533345 + TCGA-D8-A3Z6-01 COSM5833147 c.1291_1292delAA p.N431fs*14 Deletion - Frameshift 16:68813466-68813467 + SH-1362 COSM5019289 c.2634C>T p.G878G Substitution - coding silent 16:68833484-68833484 + 15 COSM1659141 c.116_117insT p.T40fs*19 Insertion - Frameshift 16:68738364-68738365 + TCGA-A7-A5ZX-01 COSM5833154 c.2191delC p.L731fs*39 Deletion - Frameshift 16:68828200-68828200 + 997337 COSM19833 c.? p.? Substitution - Missense TCGA-B5-A11E-01 COSM994818 c.659C>T p.T220M Substitution - Missense 19:3530796-3530796 + 1001726 COSM20836 c.1881_1888delAGCAGAAC p.A628fs*32 Deletion - Frameshift 16:68822170-68822177 + HCC76T COSM3707041 c.1024C>G p.H342D Substitution - Missense 19:3532432-3532432 + TCGA-BR-6452-01 COSM4062185 c.2071G>A p.A691T Substitution - Missense 16:68823533-68823533 + 45T COSM5576278 c.666_677del12 p.R222_A226>S Complex - deletion inframe 16:68808827-68808838 + 7 COSM19530 c.? p.? Unknown pfg277T COSM4756929 c.1645G>T p.D549Y Substitution - Missense 16:68819359-68819359 + 997116 COSM19769 c.884C>T p.T295I Substitution - Missense 16:68811735-68811735 + TCGA-D8-A27I-01 COSM5226736 c.494delA p.N166fs*49 Deletion - Frameshift 16:68808530-68808530 + 999879 COSM19749 c.1436A>G p.D479G Substitution - Missense 16:68815630-68815630 + T3152 COSM4686005 c.40G>A p.V14I Substitution - Missense 19:3523029-3523029 + JROECL47 COSM19819 c.357delG p.H121fs*94 Deletion - Frameshift 16:68801863-68801863 + 992983 COSM19507 c.362A>G p.H121R Substitution - Missense 16:68801868-68801868 + 2233643 COSM4172495 c.? p.T599_I600del Deletion - In frame 61 COSM5741346 c.607G>A p.V203M Substitution - Missense 19:3527767-3527767 + UM-SCC-17B COSM4593024 c.947T>G p.V316G Substitution - Missense 19:3532034-3532034 + TCGA-B5-A11E-01 COSM972798 c.2074G>A p.A692T Substitution - Missense 16:68823536-68823536 + ESO-1133 COSM1252911 c.386delC p.T129fs*77 Deletion - Frameshift 19:3526385-3526385 + Ad4 COSM4441017 c.337G>T p.E113* Substitution - Nonsense 19:3526336-3526336 + IPH-926 COSM28934 c.240_241insGGTG p.V82fs*13 Insertion - Frameshift 16:68801746-68801747 + 992997 COSM19509 c.2410delC p.D805fs*11 Deletion - Frameshift 16:68829768-68829768 + 1 COSM19785 c.786_794CACCCAGGA>T p.T263fs*3 Complex - frameshift 16:68810295-68810303 + 996949 COSM19758 c.1774G>A p.A592T Substitution - Missense 16:68822063-68822063 + D-12 COSM19503 c.67C>T p.Q23* Substitution - Nonsense 16:68738315-68738315 + NCI-H716 COSM1379142 c.670C>T p.R224C Substitution - Missense 16:68808831-68808831 + 2280424 COSM4381092 c.? p.P159_F171>L Complex - deletion inframe PD11342a COSM5752157 c.1025delC p.L343fs*13 Deletion - Frameshift 16:68812151-68812151 + KATOIII COSM20795 c.1008G>A p.E336E Substitution - coding silent 16:68811859-68811859 + TCGA-AP-A0LT-01 COSM972796 c.1997A>G p.N666S Substitution - Missense 16:68823459-68823459 + HCC25T COSM1612053 c.670G>A p.D224N Substitution - Missense 19:3530807-3530807 + TCGA-A7-A426-01 COSM3818355 c.2183T>A p.L728* Substitution - Nonsense 16:68828192-68828192 + J33_T COSM3957751 c.1496T>G p.F499C Substitution - Missense 16:68815690-68815690 + 83T COSM2996771 c.1244T>C p.I415T Substitution - Missense 16:68813419-68813419 + 2530678 COSM4281477 c.464A>G p.N155S Substitution - Missense 19:3527056-3527056 + 2280423 COSM4381092 c.? p.P159_F171>L Complex - deletion inframe CSB28 COSM5028163 c.1607_1621del15 p.N536_A541>T Complex - deletion inframe 16:68819321-68819335 + TCGA-D9-A1JX-06 COSM3532355 c.252C>A p.N84K Substitution - Missense 19:3526176-3526176 + PD9597a COSM19780 c.763C>T p.Q255* Substitution - Nonsense 16:68810272-68810272 + TCGA-IR-A3LH-01 COSM4833222 c.2455G>A p.D819N Substitution - Missense 16:68833305-68833305 + SNU-C2B COSM4281484 c.1084G>A p.A362T Substitution - Missense 19:3532492-3532492 + I2L-P19Ta-Tumor-Organoid COSM5364939 c.1294T>G p.S432A Substitution - Missense 19:3533345-3533345 + TCGA-EE-A20C-06 COSM3532358 c.515C>T p.S172F Substitution - Missense 19:3527675-3527675 + HN_63058 COSM127093 c.687+2T>G p.? Unknown 16:68808850-68808850 + 16957 COSM5029218 c.163+1_163+2insT p.? Unknown 16:68738412-68738413 + TCGA-B0-4714-01 COSM3361977 c.2210T>A p.V737D Substitution - Missense 16:68828219-68828219 + TARGET-30-PASEGA COSM1285092 c.698C>A p.T233N Substitution - Missense 19:3530835-3530835 + TCGA-A6-5661-01 COSM1379154 c.866C>T p.A289V Substitution - Missense 16:68811717-68811717 + ESO-669 COSM1247781 c.1759G>T p.D587Y Substitution - Missense 16:68822048-68822048 + 10 COSM1659148 c.2287G>T p.E763* Substitution - Nonsense 16:68828296-68828296 + 2492722 COSM5722784 c.699C>T p.T233T Substitution - coding silent 19:3530836-3530836 + BT1018 COSM19526 c.459delG p.R154fs*61 Deletion - Frameshift 16:68808495-68808495 + TCGA-BR-A4IV-01 COSM19516 c.760G>T p.D254Y Substitution - Missense 16:68810269-68810269 + MPE600 COSM35883 c.1138-21_1138del22 p.? Unknown 16:68813292-68813313 + TCGA-A8-A09X-01 COSM435595 c.871delG p.D291fs*3 Deletion - Frameshift 16:68811722-68811722 + TCGA-AC-A3W6-01 COSM384308 c.846G>T p.M282I Substitution - Missense 16:68811697-68811697 + TCGA-A2-A1FV-01 COSM1479021 c.478_479insG p.P160fs*8 Insertion - Frameshift 16:68808514-68808515 + 15721 COSM5029229 c.1986_1987delCT p.D662fs*10 Deletion - Frameshift 16:68823448-68823449 + 74 COSM4778131 c.2399G>C p.R800P Substitution - Missense 16:68829757-68829757 + S1TP COSM1159626 c.1198G>A p.D400N Substitution - Missense 16:68813373-68813373 + pfg008T COSM19494 c.372delC p.P126fs*89 Deletion - Frameshift 16:68801878-68801878 + 15 COSM20784 c.49_50insAG p.V17fs*40 Insertion - Frameshift 16:68738297-68738298 + 2318503 COSM4476805 c.209C>T p.S70F Substitution - Missense 16:68801715-68801715 + 997763 COSM19799 c.1215_1216insNNNNN p.T406fs*13 Insertion - Frameshift 16:68813390-68813391 + 103844 COSM94052 c.1654G>A p.D552N Substitution - Missense 16:68819368-68819368 + BT1023 COSM19542 c.2440-1G>A p.? Unknown 16:68833289-68833289 + PCSI_0083_Pa_P_526 COSM3787636 c.1064T>C p.L355P Substitution - Missense 19:3532472-3532472 + 105353 COSM94051 c.760G>C p.D254H Substitution - Missense 16:68810269-68810269 + 52 COSM20790 c.1711+1G>C p.? Unknown 16:68819426-68819426 + 2318503 COSM3818354 c.1921C>T p.Q641* Substitution - Nonsense 16:68822210-68822210 + 1530111 COSM96851 c.163G>C p.V55L Substitution - Missense 16:68738411-68738411 + SM12 COSM166360 c.? p.R74* Substitution - Nonsense STC263 COSM4281496 c.1334G>A p.R445H Substitution - Missense 19:3533385-3533385 + SNUH_G76_S1 COSM3755010 c.2076T>C p.A692A Substitution - coding silent 16:68823538-68823538 + S12-22512-TP COSM4990898 c.2320A>C p.R774R Substitution - coding silent 16:68829678-68829678 + ESO-580 COSM1247780 c.760G>A p.D254N Substitution - Missense 16:68810269-68810269 + MDA-MB-134VI COSM19830 c.?_?del? p.? Unknown TCGA-A2-A0YK-01 COSM435585 c.187C>T p.R63* Substitution - Nonsense 16:68801693-68801693 + TCGA-LL-A50Y-01 COSM19503 c.67C>T p.Q23* Substitution - Nonsense 16:68738315-68738315 + TCGA-B5-A11G-01 COSM972794 c.1817A>T p.N606I Substitution - Missense 16:68822106-68822106 + 587316 COSM1207723 c.1430G>A p.R477H Substitution - Missense 19:3534503-3534503 + 16590 COSM5029217 c.79delC p.C28fs*28 Deletion - Frameshift 16:68738327-68738327 + 22 COSM20787 c.1836delA p.N613fs*18 Deletion - Frameshift 16:68822125-68822125 + 997048 COSM19764 c.207_208insA p.S70fs*24 Insertion - Frameshift 16:68801713-68801714 + PD4137a COSM159879 c.1679C>G p.T560R Substitution - Missense 16:68819393-68819393 + BRC38 COSM5028160 c.1137+1G>A p.? Unknown 16:68812264-68812264 + 992969 COSM19501 c.2355C>T p.N785N Substitution - coding silent 16:68829713-68829713 + 996990 COSM19761 c.1196_1199delCTGA p.T399fs*17 Deletion - Frameshift 16:68813371-68813374 + 1001716 COSM20829 c.1320+1G>C p.? Unknown 16:68813496-68813496 + CHC320T COSM217163 c.1333C>G p.R445G Substitution - Missense 19:3533384-3533384 + TCGA-KK-A6E8-01 COSM4879157 c.1792C>G p.R598G Substitution - Missense 16:68822081-68822081 + DM59 COSM5608068 c.2296G>A p.D766N Substitution - Missense 16:68829654-68829654 + E34458 COSM19821 c.1018A>G p.T340A Substitution - Missense 16:68812144-68812144 + 14 COSM1659151 c.1957A>T p.K653* Substitution - Nonsense 16:68823419-68823419 + 996866 COSM19746 c.1742T>C p.L581P Substitution - Missense 16:68822031-68822031 + TCGA-BH-A0E9-01 COSM435608 c.2266_2267insAT p.E757fs*14 Insertion - Frameshift 16:68828275-68828276 + GC_299T1-GC_299N COSM4772557 c.447C>T p.L149L Substitution - coding silent 16:68808483-68808483 + HN_01000 COSM123292 c.1049A>T p.Q350L Substitution - Missense 19:3532457-3532457 + TCGA-D1-A16R-01 COSM994817 c.280_284delCTGCT p.L94fs*3 Deletion - Frameshift 19:3526279-3526283 + TCGA-A8-A0A7-01 COSM435592 c.727G>A p.E243K Substitution - Missense 16:68810236-68810236 + CHC2034T COSM4789846 c.1959G>T p.K653N Substitution - Missense 16:68823421-68823421 + C086 COSM5531540 c.524C>T p.P175L Substitution - Missense 19:3527684-3527684 + TCGA-D7-8572-01 COSM143801 c.1204G>C p.D402H Substitution - Missense 16:68813379-68813379 + PD7238a COSM5752866 c.493_494insA p.N166fs*2 Insertion - Frameshift 16:68808529-68808530 + 997042 COSM19766 c.1711G>A p.G571S Substitution - Missense 16:68819425-68819425 + TCGA-EE-A2GO-06 COSM3532363 c.1328C>T p.S443F Substitution - Missense 19:3533379-3533379 + BT837 COSM19532 c.1548_1560del13 p.F516fs*2 Deletion - Frameshift 16:68815742-68815754 + TCGA-B5-A0JY-01 COSM972780 c.388-2A>G p.? Unknown 16:68808422-68808422 + CHC465T COSM3668242 c.1450T>A p.S484T Substitution - Missense 19:3534804-3534804 + UM-SCC-17B COSM4593023 c.947T>G p.V316G Substitution - Missense 19:3532034-3532034 + EVSA-T COSM19825 c.687+1_687+2delGT p.? Unknown 16:68808849-68808850 + LUAD-YINHD COSM349233 c.2533C>G p.L845V Substitution - Missense 16:68833383-68833383 + VACO4S COSM19752 c.1000G>C p.D334H Substitution - Missense 16:68811851-68811851 + PTC-7C COSM4129242 c.1896C>T p.H632H Substitution - coding silent 16:68822185-68822185 + TCGA-AR-A2LN-01 COSM20785 c.371_372insC p.P127fs*41 Insertion - Frameshift 16:68801877-68801878 + CHC320T COSM217163 c.1333C>G p.R445G Substitution - Missense 19:3533384-3533384 + TCGA-BR-4279-01 COSM4062178 c.664A>G p.R222G Substitution - Missense 16:68808825-68808825 + 2492721 COSM5722784 c.699C>T p.T233T Substitution - coding silent 19:3530836-3530836 + 2492708 COSM5718456 c.855G>T p.S285S Substitution - coding silent 19:3531942-3531942 + 992989 COSM19519 c.1800A>G p.I600M Substitution - Missense 16:68822089-68822089 + 999878 COSM19748 c.1108G>C p.D370H Substitution - Missense 16:68812234-68812234 + BT937 COSM19536 c.1861delC p.N622fs*9 Deletion - Frameshift 16:68822150-68822150 + 13 COSM19785 c.786_794CACCCAGGA>T p.T263fs*3 Complex - frameshift 16:68810295-68810303 + MKN45 COSM20824 c.823_832+8del18 p.? Unknown 16:68810332-68810349 + 1009 COSM5730714 c.2072C>T p.A691V Substitution - Missense 16:68823534-68823534 + 6 COSM1659131 c.1063delT p.L355fs*1 Deletion - Frameshift 16:68812189-68812189 + BCM723T COSM5348162 c.1124delG p.G375fs*14 Deletion - Frameshift 19:3532532-3532532 + YUPEET COSM1711608 c.937C>T p.R313W Substitution - Missense 19:3532024-3532024 + 16959 COSM5029225 c.1141A>T p.K381* Substitution - Nonsense 16:68813316-68813316 + TCGA-AA-3713-01 COSM3692625 c.870C>T p.D290D Substitution - coding silent 19:3531957-3531957 + 53 COSM20785 c.371_372insC p.P127fs*41 Insertion - Frameshift 16:68801877-68801878 + TCGA-A5-A0VO-01 COSM972792 c.1711delG p.G571fs*13 Deletion - Frameshift 16:68819425-68819425 + 2324569 COSM1379142 c.670C>T p.R224C Substitution - Missense 16:68808831-68808831 + DM6 COSM5608069 c.2416G>A p.E806K Substitution - Missense 16:68829774-68829774 + 2395174 COSM5045077 c.? p.Q641* Substitution - Nonsense 127T COSM5576005 c.810C>G p.H270Q Substitution - Missense 19:3531803-3531803 + TCGA-AR-A2LL-01 COSM3818346 c.832G>A p.G278R Substitution - Missense 16:68810341-68810341 + BT1015 COSM19535 c.1844delT p.I615fs*16 Deletion - Frameshift 16:68822133-68822133 + HN_62374 COSM120855 c.2574C>A p.D858E Substitution - Missense 16:68833424-68833424 + Gp2D COSM19494 c.372delC p.P126fs*89 Deletion - Frameshift 16:68801878-68801878 + 1001723 COSM20833 c.469_531del63 p.V157_Q177del21 Deletion - In frame 16:68808505-68808567 + LUAD-NYU330 COSM391990 c.241delA p.T81fs*125 Deletion - Frameshift 19:3526165-3526165 + TCGA-D8-A1XO-01 COSM19503 c.67C>T p.Q23* Substitution - Nonsense 16:68738315-68738315 + Pat_31_A COSM1379142 c.670C>T p.R224C Substitution - Missense 16:68808831-68808831 + 1 COSM1659137 c.110_111insA p.Y37fs*1 Insertion - Frameshift 16:68738358-68738359 + T14 COSM19780 c.763C>T p.Q255* Substitution - Nonsense 16:68810272-68810272 + 18161 COSM5029221 c.749_750insCAC p.T251_V252insT Insertion - In frame 16:68810258-68810259 + TCGA-KK-A59V-01 COSM4878136 c.1068G>A p.A356A Substitution - coding silent 19:3532476-3532476 + C086 COSM5531539 c.524C>T p.P175L Substitution - Missense 19:3527684-3527684 + TCGA-A8-A0A9-01 COSM435600 c.1507C>T p.Q503* Substitution - Nonsense 16:68815701-68815701 + SJMB002 COSM255866 c.187C>G p.R63G Substitution - Missense 16:68801693-68801693 + P104x COSM133647 c.1_2649del2649 p.0? Whole gene deletion TCGA-EW-A3E8-01 COSM5833152 c.2162_2164+1delTAAG p.? Unknown 16:68823624-68823627 + SK-BR-3 COSM20798 c.?_?del? p.? Unknown P0006 COSM5885246 c.? p.Q23* Substitution - Nonsense CSCC-55-T COSM4530918 c.173G>A p.S58N Substitution - Missense 19:3525971-3525971 + B88 COSM1749723 c.2191C>T p.L731F Substitution - Missense 16:68828200-68828200 + PT49 COSM5936193 c.475C>T p.P159S Substitution - Missense 16:68808511-68808511 + TCGA-D8-A1JN-01 COSM1479027 c.1774_1775insC p.I594fs*11 Insertion - Frameshift 16:68822063-68822064 + pfg263T COSM4756924 c.539C>T p.S180F Substitution - Missense 16:68808700-68808700 + LIM1899 COSM4640069 c.2196G>A p.R732R Substitution - coding silent 16:68828205-68828205 + PD7214a COSM5801631 c.905_906insA p.Y302fs*1 Insertion - Frameshift 16:68811756-68811757 + RPMI-8226 COSM1679223 c.2450C>T p.A817V Substitution - Missense 16:68833300-68833300 + 993002 COSM19514 c.185G>A p.G62D Substitution - Missense 16:68801691-68801691 + PD14460a COSM5780488 c.113C>T p.T38M Substitution - Missense 16:68738361-68738361 + LP6005334-DNA_G03 COSM435592 c.727G>A p.E243K Substitution - Missense 16:68810236-68810236 + PD4121a COSM165999 c.1215_1234del20 p.T406fs*6 Deletion - Frameshift 16:68813390-68813409 + 20 COSM1659135 c.2189delT p.L731fs*39 Deletion - Frameshift 16:68828198-68828198 + BRC39 COSM5028157 c.412G>A p.E138K Substitution - Missense 16:68808448-68808448 + I2L-P19Tb-Tumor-Biopsy COSM5363428 c.1501G>A p.V501M Substitution - Missense 16:68815695-68815695 + Au4 COSM5603627 c.195+1G>C p.? Unknown 19:3525994-3525994 + TCGA-AZ-6605-01 COSM1379191 c.2184G>A p.L728L Substitution - coding silent 16:68828193-68828193 + T3610 COSM4686007 c.253G>A p.G85S Substitution - Missense 19:3526177-3526177 + TCGA-OL-A5RV-01 COSM3818353 c.1534G>T p.E512* Substitution - Nonsense 16:68815728-68815728 + C086 COSM5531542 c.525C>T p.P175P Substitution - coding silent 19:3527685-3527685 + TCGA-KK-A59V-01 COSM4878135 c.1068G>A p.A356A Substitution - coding silent 19:3532476-3532476 + 993146 COSM19520 c.1595G>A p.W532* Substitution - Nonsense 16:68819309-68819309 + AOCS-058-1-5 COSM4140506 c.404A>C p.K135T Substitution - Missense 19:3526996-3526996 + 5 COSM20786 c.1519_1525delTCCTACA p.S507fs*13 Deletion - Frameshift 16:68815713-68815719 + T3058 COSM19773 c.1019C>T p.T340M Substitution - Missense 16:68812145-68812145 + TCGA-BR-4184-01 COSM4076872 c.32G>A p.R11H Substitution - Missense 19:3523021-3523021 + SC-her2-036 COSM4777510 c.191_192insCT p.Q64fs*2 Insertion - Frameshift 16:68801697-68801698 + DM2 COSM5608067 c.2350C>T p.R784C Substitution - Missense 16:68829708-68829708 + PD13607a COSM5801554 c.600_601insGT p.P201fs*15 Insertion - Frameshift 16:68808761-68808762 + TCGA-OL-A66K-01 COSM5833149 c.1722_1723insG p.A575fs*13 Insertion - Frameshift 16:68822011-68822012 + 1618319 COSM143801 c.1204G>C p.D402H Substitution - Missense 16:68813379-68813379 + 999880 COSM19750 c.1204G>A p.D402N Substitution - Missense 16:68813379-68813379 + 997330 COSM19779 c.893C>A p.A298D Substitution - Missense 16:68811744-68811744 + PD7214a COSM5752865 c.904_905insA p.Y302fs*1 Insertion - Frameshift 16:68811755-68811756 + MDA-N COSM1679221 c.568T>C p.Y190H Substitution - Missense 16:68808729-68808729 + TCGA-A8-A07B-01 COSM3818343 c.600C>A p.P200P Substitution - coding silent 16:68808761-68808761 + TCGA-BS-A0TE-01 COSM972774 c.284A>T p.Q95L Substitution - Missense 16:68801790-68801790 + COGA-3 COSM19822 c.1901C>T p.A634V Substitution - Missense 16:68822190-68822190 + 997118 COSM19772 c.900C>G p.I300M Substitution - Missense 16:68811751-68811751 + STC263 COSM3197055 c.1334G>A p.R445H Substitution - Missense 19:3533385-3533385 + 17929 COSM5029232 c.2127_2134delCATTCTGG p.I710fs*35 Deletion - Frameshift 16:68823589-68823596 + CSB12 COSM5028159 c.971_975delGAGTC p.G324fs*24 Deletion - Frameshift 16:68811822-68811826 + ESCC_141 COSM4281481 c.1041C>T p.P347P Substitution - coding silent 19:3532449-3532449 + HCT116 COSM19819 c.357delG p.H121fs*94 Deletion - Frameshift 16:68801863-68801863 + PD6051a COSM4384876 c.269G>A p.R90Q Substitution - Missense 16:68801775-68801775 + T3021 COSM4670765 c.734_735insA p.M246fs*12 Insertion - Frameshift 16:68810243-68810244 + C086 COSM5531541 c.525C>T p.P175P Substitution - coding silent 19:3527685-3527685 + 997060 COSM19768 c.846_867del22 p.E283fs*4 Deletion - Frameshift 16:68811697-68811718 + S06-38853-TP COSM4990896 c.2220C>T p.P740P Substitution - coding silent 16:68828229-68828229 + Pat_40_A COSM5855456 c.703G>A p.V235M Substitution - Missense 19:3530840-3530840 + I-03 COSM4766271 c.662A>G p.D221G Substitution - Missense 16:68808823-68808823 + 2492709 COSM5718455 c.855G>T p.S285S Substitution - coding silent 19:3531942-3531942 + 999882 COSM20773 c.1040C>T p.A347V Substitution - Missense 16:68812166-68812166 + LUAD-RT-S01831 COSM384308 c.846G>T p.M282I Substitution - Missense 16:68811697-68811697 + PD4205a COSM159884 c.1342C>T p.Q448* Substitution - Nonsense 16:68815536-68815536 + TCGA-AR-A2LJ-01 COSM4815195 c.493G>C p.E165Q Substitution - Missense 16:68808529-68808529 + C0100T COSM4154167 c.1449+10A>G p.? Unknown 19:3534532-3534532 + 142T COSM2996774 c.1320+1G>A p.? Unknown 16:68813496-68813496 + TCGA-A2-A0T6-01 COSM435611 c.2480_2481insTGAT p.S829fs*1 Insertion - Frameshift 16:68833330-68833331 + TCGA-B6-A40B-01 COSM159883 c.1480G>T p.E494* Substitution - Nonsense 16:68815674-68815674 + 2492708 COSM5718455 c.855G>T p.S285S Substitution - coding silent 19:3531942-3531942 + SJMB131 COSM255228 c.985G>T p.V329F Substitution - Missense 16:68811836-68811836 + 21 COSM143802 c.1223C>T p.A408V Substitution - Missense 16:68813398-68813398 + 7 COSM1659132 c.1041delT p.A348fs*8 Deletion - Frameshift 16:68812167-68812167 + CAL27 COSM4593024 c.947T>G p.V316G Substitution - Missense 19:3532034-3532034 + PD4194a COSM219704 c.86_89ACCC>GTG p.H29fs*27 Complex - frameshift 16:68738334-68738337 + DM10 COSM5608065 c.187C>A p.R63R Substitution - coding silent 16:68801693-68801693 + TCGA-E2-A1L8-01 COSM1479023 c.832+1G>A p.? Unknown 16:68810342-68810342 + 1001692 COSM20827 c.? p.Y380_K440del Deletion - In frame 997040 COSM19765 c.60_79del20 p.W20fs*7 Deletion - Frameshift 16:68738308-68738327 + PTC-14C COSM4131640 c.288G>T p.K96N Substitution - Missense 19:3526287-3526287 + 999864 COSM19753 c.1009-1G>A p.? Unknown 16:68812134-68812134 + TCGA-CG-4474-01 COSM4062176 c.563T>A p.V188D Substitution - Missense 16:68808724-68808724 + TCGA-NI-A4U2-01 COSM4909641 c.9G>A p.Q3Q Substitution - coding silent 19:3522998-3522998 + KM12 COSM4612772 c.989_990insG p.N333fs*47 Insertion - Frameshift 19:3532076-3532077 + SC-her2-014 COSM4771414 c.2416G>T p.E806* Substitution - Nonsense 16:68829774-68829774 + SNU-C4 COSM4653099 c.1111C>A p.L371M Substitution - Missense 19:3532519-3532519 + 992985 COSM19510 c.2125G>A p.A709T Substitution - Missense 16:68823587-68823587 + PCSI_0085_Pa_P_526 COSM4961714 c.387+10C>T p.? Unknown 19:3526396-3526396 + C135 COSM4617690 c.1373A>T p.N458I Substitution - Missense 16:68815567-68815567 + CHC320T COSM5349149 c.1333C>G p.R445G Substitution - Missense 19:3533384-3533384 + pfg416T COSM4747421 c.558_575del18 p.K187_I192delKVFYSI Deletion - In frame 16:68808719-68808736 + 2521244 COSM5887489 c.1250C>T p.T417M Substitution - Missense 19:3533301-3533301 + TCGA-A8-A07B-01 COSM5833142 c.598delC p.P201fs*14 Deletion - Frameshift 16:68808759-68808759 + 993000 COSM19511 c.1323_1333del11 p.L442fs*18 Deletion - Frameshift 16:68815517-68815527 + pfg368T COSM19516 c.760G>T p.D254Y Substitution - Missense 16:68810269-68810269 + TCGA-BP-5187-01 COSM471991 c.2246G>A p.R749Q Substitution - Missense 16:68828255-68828255 + TCGA-EE-A29E-06 COSM3511254 c.2156C>T p.A719V Substitution - Missense 16:68823618-68823618 + B34 COSM1749722 c.1914G>A p.W638* Substitution - Nonsense 16:68822203-68822203 + TCGA-AN-A03Y-01 COSM435585 c.187C>T p.R63* Substitution - Nonsense 16:68801693-68801693 + BCT-B-B7 COSM19493 c.846G>A p.M282I Substitution - Missense 16:68811697-68811697 + SJMB137 COSM255229 c.1477G>C p.V493L Substitution - Missense 16:68815671-68815671 + TCGA-22-1016-01 COSM704381 c.211C>T p.L71F Substitution - Missense 16:68801717-68801717 + HCC028T COSM5807628 c.423A>T p.T141T Substitution - coding silent 16:68808459-68808459 + PD11375a COSM5752168 c.2532_2533delTC p.L845fs*15 Deletion - Frameshift 16:68833382-68833383 + 2198694 COSM3768905 c.? p.R54G Substitution - Missense SH-3776 COSM5019289 c.2634C>T p.G878G Substitution - coding silent 16:68833484-68833484 + TCGA-CD-A4MG-01 COSM19513 c.1676G>A p.S559N Substitution - Missense 16:68819390-68819390 + PT35 COSM5913741 c.1754T>A p.L585Q Substitution - Missense 16:68822043-68822043 + TCGA-A2-A0EX-01 COSM435602 c.1531C>T p.Q511* Substitution - Nonsense 16:68815725-68815725 + PD4877a COSM19822 c.1901C>T p.A634V Substitution - Missense 16:68822190-68822190 + 992987 COSM19512 c.1366G>A p.V456M Substitution - Missense 16:68815560-68815560 + TCGA-BH-A0BA-01 COSM435593 c.779C>A p.P260H Substitution - Missense 16:68810288-68810288 + CSCC-19-T COSM4476805 c.209C>T p.S70F Substitution - Missense 16:68801715-68801715 + BT699 COSM19528 c.786_787insA p.T263fs*6 Insertion - Frameshift 16:68810295-68810296 + 18 COSM19503 c.67C>T p.Q23* Substitution - Nonsense 16:68738315-68738315 + YUWAND COSM1711610 c.1433C>T p.S478L Substitution - Missense 19:3534506-3534506 + LS411 COSM3197033 c.426C>T p.G142G Substitution - coding silent 19:3527018-3527018 + PD5960a COSM5752675 c.2164+1G>T p.? Unknown 16:68823627-68823627 + ESCC-002T COSM3937139 c.1266A>G p.Q422Q Substitution - coding silent 16:68813441-68813441 + GC_356T-GC_356N COSM4774643 c.523_531+17del26 p.? Unknown 16:68808559-68808584 + TCGA-EJ-7782-01 COSM3782980 c.745T>G p.L249V Substitution - Missense 16:68810254-68810254 + 61 COSM5741348 c.782G>T p.G261V Substitution - Missense 19:3531775-3531775 + 1001665 COSM20774 c.1418T>A p.V473D Substitution - Missense 16:68815612-68815612 + TCGA-BR-8058-01 COSM19516 c.760G>T p.D254Y Substitution - Missense 16:68810269-68810269 + TCGA-EW-A1J2-01 COSM1479034 c.2002A>T p.K668* Substitution - Nonsense 16:68823464-68823464 + TCGA-DY-A1H8-01 COSM5077741 c.484C>T p.R162W Substitution - Missense 19:3527644-3527644 + 1530118 COSM96853 c.548_549delAC p.D183fs*15 Deletion - Frameshift 16:68808709-68808710 + TCGA-FP-A4BE-01 COSM4076871 c.23G>A p.R8H Substitution - Missense 19:3523012-3523012 + pfg015T COSM1640536 c.379delC p.H128fs*87 Deletion - Frameshift 16:68801885-68801885 + TCGA-EE-A29D-06 COSM3511251 c.798C>T p.V266V Substitution - coding silent 16:68810307-68810307 + BT1004 COSM19527 c.761_777del17 p.D254fs*9 Deletion - Frameshift 16:68810270-68810286 + pfg413T COSM4062185 c.2071G>A p.A691T Substitution - Missense 16:68823533-68823533 + 996889 COSM19757 c.1320+?del? p.? Unknown SUM44PE COSM19827 c.1269delT p.F423fs*8 Deletion - Frameshift 16:68813444-68813444 + 996869 COSM19749 c.1436A>G p.D479G Substitution - Missense 16:68815630-68815630 + KM12 COSM4639035 c.818G>A p.R273H Substitution - Missense 19:3531811-3531811 + 997334 COSM19781 c.734C>T p.P245L Substitution - Missense 16:68810243-68810243 + PD7204a COSM5752862 c.342_343insA p.T115fs*53 Insertion - Frameshift 16:68801848-68801849 + pfg122T COSM19494 c.372delC p.P126fs*89 Deletion - Frameshift 16:68801878-68801878 + COGA-3 COSM19823 c.602delC p.P201fs*14 Deletion - Frameshift 16:68808763-68808763 + PD14465a COSM5752253 c.651_652delAG p.E218fs*4 Deletion - Frameshift 16:68808812-68808813 + TCGA-A8-A09V-01 COSM435588 c.499_500insCCC p.E167>AQ Complex - insertion inframe 16:68808535-68808536 + SK-BR-3 COSM35881 c.1_1936del1936 p.? Unknown TCGA-DA-A1I7-06 COSM3532361 c.591C>A p.S197S Substitution - coding silent 19:3527751-3527751 + UM-SCC-2 COSM4593024 c.947T>G p.V316G Substitution - Missense 19:3532034-3532034 + ESCC_157 COSM5646278 c.765G>C p.Q255H Substitution - Missense 16:68810274-68810274 + TCGA-AC-A3TN-01 COSM3818342 c.583C>T p.Q195* Substitution - Nonsense 16:68808744-68808744 + 1530119 COSM96855 c.2294_2295insA p.D766fs*3 Insertion - Frameshift 16:68828303-68828304 + PD11342a COSM5752157 c.1025delC p.L343fs*13 Deletion - Frameshift 16:68812151-68812151 + 1179078 COSM28934 c.240_241insGGTG p.V82fs*13 Insertion - Frameshift 16:68801746-68801747 + PD14442a COSM19486 c.2095C>T p.Q699* Substitution - Nonsense 16:68823557-68823557 + TCGA-B6-A0RQ-01 COSM19503 c.67C>T p.Q23* Substitution - Nonsense 16:68738315-68738315 + GC_337T-GC_337N COSM4771876 c.1777C>T p.P593S Substitution - Missense 16:68822066-68822066 + PCSI_0105_Pa_P_526 COSM4962212 c.802G>C p.E268Q Substitution - Missense 19:3531795-3531795 + TCGA-RC-A7S9-01 COSM4940249 c.1389G>A p.E463E Substitution - coding silent 16:68815583-68815583 + TCGA-D5-6928-01 COSM1379140 c.263C>A p.P88H Substitution - Missense 16:68801769-68801769 + 1452529 COSM51517 c.1282A>G p.N428D Substitution - Missense 16:68813457-68813457 + WSU-HN6 COSM4593023 c.947T>G p.V316G Substitution - Missense 19:3532034-3532034 + 1001722 COSM20838 c.1009_1137del129 p.S337_T379del43 Deletion - In frame 16:68812135-68812263 + TCGA-AX-A06L-01 COSM972800 c.2195G>A p.R732Q Substitution - Missense 16:68828204-68828204 + 1179079 COSM28934 c.240_241insGGTG p.V82fs*13 Insertion - Frameshift 16:68801746-68801747 + TCGA-CD-5813-01 COSM4062182 c.1006G>A p.E336K Substitution - Missense 16:68811857-68811857 + TCGA-BH-A209-01 COSM435585 c.187C>T p.R63* Substitution - Nonsense 16:68801693-68801693 + PD14442a COSM19486 c.2095C>T p.Q699* Substitution - Nonsense 16:68823557-68823557 + 996988 COSM19761 c.1196_1199delCTGA p.T399fs*17 Deletion - Frameshift 16:68813371-68813374 + ESO-0129 COSM1252912 c.576G>C p.L192L Substitution - coding silent 19:3527736-3527736 + HCC18 COSM1609555 c.427C>T p.P143S Substitution - Missense 16:68808463-68808463 + BN24 COSM1609556 c.1161C>T p.N387N Substitution - coding silent 16:68813336-68813336 + I2L-P19Ta-Tumor-Organoid COSM5364938 c.1294T>G p.S432A Substitution - Missense 19:3533345-3533345 + PD4203a COSM159880 c.1468G>A p.E490K Substitution - Missense 16:68815662-68815662 + ZR75-30 COSM19419 c.727G>T p.E243* Substitution - Nonsense 16:68810236-68810236 + OST201PT COSM1732281 c.332C>T p.S111F Substitution - Missense 16:68801838-68801838 + D-02 COSM4766182 c.767A>G p.N256S Substitution - Missense 16:68810276-68810276 + LUAD-E00934 COSM393288 c.2474C>T p.P825L Substitution - Missense 16:68833324-68833324 + 1001721 COSM19505 c.164_387del224 p.V55fs*38 Deletion - Frameshift TCGA-AD-6964-01 COSM1379190 c.2053G>A p.V685M Substitution - Missense 16:68823515-68823515 + pfg151T COSM4747422 c.602_628del27 p.P201_E210>Q Complex - deletion inframe 16:68808763-68808789 + TCGA-C8-A1HO-01 COSM1479031 c.1930G>A p.D644N Substitution - Missense 16:68822219-68822219 + TCGA-BR-A453-01 COSM4062184 c.1320G>T p.K440N Substitution - Missense 16:68813495-68813495 + CHC1704T COSM4804144 c.407G>T p.R136L Substitution - Missense 19:3526999-3526999 + 996992 COSM19760 c.1156G>T p.E386* Substitution - Nonsense 16:68813331-68813331 + PD4194a COSM1379133 c.88C>T p.P30S Substitution - Missense 16:68738336-68738336 + 997117 COSM19770 c.1027C>T p.L343L Substitution - coding silent 16:68812153-68812153 + CHC320T COSM217163 c.1333C>G p.R445G Substitution - Missense 19:3533384-3533384 + PD7027a COSM4384877 c.1183A>G p.T395A Substitution - Missense 16:68813358-68813358 + TCGA-EE-A2A6-06 COSM3511255 c.2230C>T p.P744S Substitution - Missense 16:68828239-68828239 + TCGA-KK-A59V-01 COSM4281458 c.82C>T p.R28W Substitution - Missense 19:3525880-3525880 + 1001718 COSM19504 c.49_163del115 p.V17fs*1 Deletion - Frameshift 16:68738297-68738411 + 2521244 COSM5887488 c.1250C>T p.T417M Substitution - Missense 19:3533301-3533301 + TCGA-AR-A5QM-01 COSM25265 c.220C>T p.R74* Substitution - Nonsense 16:68801726-68801726 + TCGA-HJ-7597-01 COSM2996754 c.699C>T p.H233H Substitution - coding silent 16:68810208-68810208 + pfg321T COSM4747423 c.687+1_687+3delGTA p.? Unknown 16:68808849-68808851 + 992733 COSM19486 c.2095C>T p.Q699* Substitution - Nonsense 16:68823557-68823557 + TCGA-BR-A44T-01 COSM4062179 c.742A>T p.I248F Substitution - Missense 16:68810251-68810251 + PD18049a COSM5801417 c.1886_1887insA p.L630fs*33 Insertion - Frameshift 16:68822175-68822176 + PD4203a COSM159881 c.1475G>T p.R492I Substitution - Missense 16:68815669-68815669 + 1855645 COSM1169611 c.1109A>G p.D370G Substitution - Missense 16:68812235-68812235 + DM10 COSM558823 c.715G>T p.G239W Substitution - Missense 16:68810224-68810224 + 1001640 COSM20822 c.1252_1269del18 p.D418_F423delDDGGQF Deletion - In frame 16:68813427-68813444 + 2492723 COSM5722785 c.699C>T p.T233T Substitution - coding silent 19:3530836-3530836 + TCGA-21-5787-01 COSM704380 c.829C>T p.P277S Substitution - Missense 16:68810338-68810338 + C086 COSM5528432 c.2510G>A p.G837E Substitution - Missense 16:68833360-68833360 + TCGA-F1-6177-01 COSM972802 c.2280C>T p.G760G Substitution - coding silent 16:68828289-68828289 + WSU-HN8 COSM4593023 c.947T>G p.V316G Substitution - Missense 19:3532034-3532034 + PD9579a COSM4756923 c.531+1G>A p.? Unknown 16:68808568-68808568 + TCGA-BR-4361-01 COSM4062172 c.276T>C p.H92H Substitution - coding silent 16:68801782-68801782 + TCGA-BR-8592-01 COSM4062177 c.569A>G p.Y190C Substitution - Missense 16:68808730-68808730 + 17738 COSM435586 c.475delC p.P159fs*56 Deletion - Frameshift 16:68808511-68808511 + TCGA-A7-A3IZ-01 COSM194600 c.1003C>T p.R335* Substitution - Nonsense 16:68811854-68811854 + 992721 COSM19485 c.944A>G p.N315S Substitution - Missense 16:68811795-68811795 + WA11 COSM239937 c.652C>T p.Q218* Substitution - Nonsense 19:3527812-3527812 + CHC465T COSM5349184 c.1459T>A p.S487T Substitution - Missense 19:3534804-3534804 + 992982 COSM19506 c.856G>A p.A286T Substitution - Missense 16:68811707-68811707 + TCGA-B0-4706-01 COSM474556 c.1287G>A p.K429K Substitution - coding silent 19:3533338-3533338 + SH-4435 COSM5020197 c.531+10G>C p.? Unknown 16:68808577-68808577 + TCGA-BR-8370-01 COSM1379150 c.769G>A p.D257N Substitution - Missense 16:68810278-68810278 + TCGA-EJ-7786-01 COSM1471047 c.523C>G p.P175A Substitution - Missense 19:3527683-3527683 + PD18756a COSM435602 c.1531C>T p.Q511* Substitution - Nonsense 16:68815725-68815725 + TCGA-A6-6780-01 COSM1379159 c.939_940insA p.N315fs*6 Insertion - Frameshift 16:68811790-68811791 + 936 COSM19492 c.2165-1G>A p.? Unknown 16:68828173-68828173 + HN_00076 COSM123293 c.1478G>A p.R493Q Substitution - Missense 19:3534832-3534832 + TCGA-D1-A163-01 COSM972778 c.375C>A p.P125P Substitution - coding silent 16:68801881-68801881 + TCGA-KK-A59V-01 COSM3197015 c.82C>T p.R28W Substitution - Missense 19:3525880-3525880 + I2L-P19Tb-Tumor-Organoid COSM5363428 c.1501G>A p.V501M Substitution - Missense 16:68815695-68815695 + PD13607a COSM5752778 c.599_600insGT p.P201fs*15 Insertion - Frameshift 16:68808760-68808761 + TCGA-BH-A0C1-01 COSM435586 c.475delC p.P159fs*56 Deletion - Frameshift 16:68808511-68808511 + 2492722 COSM5722785 c.699C>T p.T233T Substitution - coding silent 19:3530836-3530836 + PD9589a COSM5752498 c.1858delC p.P620fs*11 Deletion - Frameshift 16:68822147-68822147 + TCGA-EB-A5UM-01 COSM3511253 c.1381C>T p.P461S Substitution - Missense 16:68815575-68815575 + TCGA-A8-A09V-01 COSM5226736 c.494delA p.N166fs*49 Deletion - Frameshift 16:68808530-68808530 + SH-9161 COSM5020197 c.531+10G>C p.? Unknown 16:68808577-68808577 + 997765 COSM19758 c.1774G>A p.A592T Substitution - Missense 16:68822063-68822063 + AGS COSM25267 c.1733_1734insC p.G579fs*9 Insertion - Frameshift 16:68822022-68822023 + 6 COSM20788 c.2047_2048delGT p.V683fs*4 Deletion - Frameshift 16:68823509-68823510 + pfg181T COSM4748922 c.734C>T p.A245V Substitution - Missense 19:3531727-3531727 + PD13763a COSM5752580 c.26C>A p.S9* Substitution - Nonsense 16:68737441-68737441 + HT115 COSM256583 c.1942G>T p.E648* Substitution - Nonsense 16:68823404-68823404 + 1001694 COSM20827 c.? p.Y380_K440del Deletion - In frame CAMA-1 COSM19824 c.1712-1G>A p.? Unknown 16:68822000-68822000 + 18154 COSM5029219 c.288delC p.H97fs*20 Deletion - Frameshift 16:68801794-68801794 + HSC45-M2 COSM19820 c.1320+2_1320+11delTTTGTATGGT p.? Unknown 16:68813497-68813506 + TCGA-AC-A2FF-01 COSM5205425 c.256_257delAA p.R87fs*6 Deletion - Frameshift 16:68801762-68801763 + 999862 COSM19748 c.1108G>C p.D370H Substitution - Missense 16:68812234-68812234 + WSU-HN6 COSM4593024 c.947T>G p.V316G Substitution - Missense 19:3532034-3532034 + PT37 COSM5920951 c.1936+4G>A p.? Unknown 16:68822229-68822229 + SNU-C4 COSM4653100 c.1111C>A p.L371M Substitution - Missense 19:3532519-3532519 + SM8E COSM166359 c.? p.P126fs*89 Unknown WSU-HN13 COSM4601866 c.488G>C p.C163S Substitution - Missense 16:68808524-68808524 + PD9063a COSM19780 c.763C>T p.Q255* Substitution - Nonsense 16:68810272-68810272 + TCGA-BR-8364-01 COSM4062175 c.524T>C p.L175P Substitution - Missense 16:68808560-68808560 + TCGA-BR-A4QM-01 COSM1247778 c.1489G>A p.E497K Substitution - Missense 16:68815683-68815683 + 1530087 COSM96848 c.1054_1058delGGTGA p.E353fs*13 Deletion - Frameshift 16:68812180-68812184 + TCGA-GM-A2DO-01 COSM3818348 c.862G>A p.D288N Substitution - Missense 16:68811713-68811713 + DM98 COSM5584743 c.75G>A p.P25P Substitution - coding silent 16:68738323-68738323 + 17208 COSM5029223 c.856_864delGCCACAGAC p.T287_A289delTDA Deletion - In frame 16:68811707-68811715 + TCGA-NI-A4U2-01 COSM4909642 c.9G>A p.Q3Q Substitution - coding silent 19:3522998-3522998 + BCT-B-E6 COSM19497 c.1890_1891insAC p.G633fs*21 Insertion - Frameshift 16:68822179-68822180 + 993006 COSM19518 c.2075C>T p.A692V Substitution - Missense 16:68823537-68823537 + BT929 COSM19498 c.866_867delCG p.A289fs*3 Deletion - Frameshift 16:68811717-68811718 + 7 COSM19785 c.786_794CACCCAGGA>T p.T263fs*3 Complex - frameshift 16:68810295-68810303 + YUKIL COSM1711609 c.1070_1071CC>TT p.A357V Substitution - Missense 19:3532478-3532479 + 2521259 COSM5890900 c.2194C>T p.R732W Substitution - Missense 16:68828203-68828203 + PD5936a COSM19798 c.1207_1208insC p.N405fs*14 Insertion - Frameshift 16:68813382-68813383 + 2218463 COSM4421278 c.1057G>T p.E353* Substitution - Nonsense 19:3532465-3532465 + PD4977a COSM1159626 c.1198G>A p.D400N Substitution - Missense 16:68813373-68813373 + 8 COSM19540 c.532-1G>T p.? Unknown 16:68808692-68808692 + Au4 COSM5603628 c.195+1G>C p.? Unknown 19:3525994-3525994 + TCGA-BF-A3DL-01 COSM4904853 c.1628C>T p.S543F Substitution - Missense 16:68819342-68819342 + TCGA-A2-A0YD-01 COSM435597 c.1014delC p.P339fs*17 Deletion - Frameshift 16:68812140-68812140 + TCGA-BS-A0UV-01 COSM972806 c.2521G>A p.E841K Substitution - Missense 16:68833371-68833371 + T1232 COSM4686013 c.1333C>T p.R445C Substitution - Missense 19:3533384-3533384 + Ad4 COSM4441016 c.337G>T p.E113* Substitution - Nonsense 19:3526336-3526336 + DGC1 COSM24348 c.377delC p.P126fs*89 Deletion - Frameshift 16:68801883-68801883 + TCGA-D8-A3Z5-01 COSM5833157 c.2369delC p.L791fs*2 Deletion - Frameshift 16:68829727-68829727 + TCGA-D3-A51T-06 COSM3532357 c.447C>T p.S149S Substitution - coding silent 19:3527039-3527039 + 22 COSM1659136 c.939_946delCAAAAATA p.K314fs*4 Deletion - Frameshift 16:68811790-68811797 + JXG-1 COSM19743 c.1849G>A p.A617T Substitution - Missense 16:68822138-68822138 + TCGA-AR-A24T-01 COSM1479033 c.1946_1947insT p.I650fs*13 Insertion - Frameshift 16:68823408-68823409 + HCC76 COSM3707041 c.1024C>G p.H342D Substitution - Missense 19:3532432-3532432 + 192T COSM4062183 c.1199A>T p.D400V Substitution - Missense 16:68813374-68813374 + S03-45671-TP COSM20775 c.2253C>T p.N751N Substitution - coding silent 16:68828262-68828262 + TCGA-E9-A3X8-01 COSM5833148 c.1544_1545insATA p.T515_F516ins* Insertion - In frame 16:68815738-68815739 + 1995691 COSM1666867 c.? p.N240fs*10 Unknown 1520 COSM19489 c.?_?insG p.?fs Insertion - Frameshift BCT-B-C9 COSM19494 c.372delC p.P126fs*89 Deletion - Frameshift 16:68801878-68801878 + TCGA-AX-A05Z-01 COSM972784 c.681A>G p.T227T Substitution - coding silent 16:68808842-68808842 + 1001707 COSM20778 c.1321_1389del69 p.G441_E463del23 Deletion - In frame 16:68815515-68815583 + TCGA-BR-4279-01 COSM1479032 c.1936+1G>T p.? Unknown 16:68822226-68822226 + TCGA-FS-A1ZK-06 COSM3511252 c.1286C>T p.P429L Substitution - Missense 16:68813461-68813461 + 11 COSM1659140 c.1947_1948insT p.I650fs*13 Insertion - Frameshift 16:68823409-68823410 + UACC-812 COSM35879 c.1565C>T p.T522I Substitution - Missense 16:68815759-68815759 + XHDG25 COSM4593023 c.947T>G p.V316G Substitution - Missense 19:3532034-3532034 + TCGA-A2-A0CK-01 COSM3818347 c.832G>T p.G278* Substitution - Nonsense 16:68810341-68810341 + C135 COSM4617691 c.1394C>A p.S465Y Substitution - Missense 16:68815588-68815588 + 1530090 COSM96849 c.136_143delCTGGAGAG p.L46fs*10 Deletion - Frameshift 16:68738384-68738391 + SA077 COSM211957 c.1829A>T p.Q610L Substitution - Missense 16:68822118-68822118 + CSCC-35-T COSM4467618 c.149C>T p.P50L Substitution - Missense 19:3525947-3525947 + pfg068T COSM4756919 c.259A>G p.R87G Substitution - Missense 16:68801765-68801765 + TCGA-F4-6570-01 COSM1379179 c.1528G>A p.A510T Substitution - Missense 16:68815722-68815722 + 19 COSM1659134 c.1532_1535delAGGA p.Q511fs*10 Deletion - Frameshift 16:68815726-68815729 + 2492720 COSM5722785 c.699C>T p.T233T Substitution - coding silent 19:3530836-3530836 + 997336 COSM19783 c.2552C>T p.S851L Substitution - Missense 16:68833402-68833402 + 032T COSM1728427 c.1333C>A p.R445S Substitution - Missense 19:3533384-3533384 + KM12 COSM4639036 c.818G>A p.R273H Substitution - Missense 19:3531811-3531811 + 10 COSM19785 c.786_794CACCCAGGA>T p.T263fs*3 Complex - frameshift 16:68810295-68810303 + 997328 COSM19778 c.2321G>A p.R774K Substitution - Missense 16:68829679-68829679 + 2492709 COSM5718456 c.855G>T p.S285S Substitution - coding silent 19:3531942-3531942 + TCGA-GM-A5PV-01 COSM19492 c.2165-1G>A p.? Unknown 16:68828173-68828173 + PD14472a COSM5752797 c.74_75insG p.E26fs*8 Insertion - Frameshift 16:68738322-68738323 + TCGA-66-2759-01 COSM704379 c.1333G>C p.E445Q Substitution - Missense 16:68815527-68815527 + MKN45 COSM20824 c.823_832+8del18 p.? Unknown 16:68810332-68810349 + 997118 COSM19773 c.1019C>T p.T340M Substitution - Missense 16:68812145-68812145 + 1001720 COSM19503 c.67C>T p.Q23* Substitution - Nonsense 16:68738315-68738315 + sysucc-823T COSM5461723 c.48+6C>T p.? Unknown 16:68737469-68737469 + IGC8 COSM24348 c.377delC p.P126fs*89 Deletion - Frameshift 16:68801883-68801883 + TCGA-HU-A4GX-01 COSM4076891 c.418G>A p.D140N Substitution - Missense 19:3527010-3527010 + 2313841 COSM4771414 c.2416G>T p.E806* Substitution - Nonsense 16:68829774-68829774 + TCGA-HT-A617-01 COSM4420757 c.1108G>A p.D370N Substitution - Missense 16:68812234-68812234 + OSCC-GB_00410111 COSM3712170 c.478C>T p.P160S Substitution - Missense 16:68808514-68808514 + TCGA-EE-A3JD-06 COSM4396713 c.1833C>T p.V611V Substitution - coding silent 16:68822122-68822122 + 993004 COSM19516 c.760G>T p.D254Y Substitution - Missense 16:68810269-68810269 + CHC798T COSM4958330 c.2277A>C p.G759G Substitution - coding silent 16:68828286-68828286 + 997118 COSM19774 c.1070C>T p.T357I Substitution - Missense 16:68812196-68812196 + KATOIII COSM20795 c.1008G>A p.E336E Substitution - coding silent 16:68811859-68811859 + 2198695 COSM3768905 c.? p.R54G Substitution - Missense TCGA-A5-A0GA-01 COSM972788 c.1207G>A p.A403T Substitution - Missense 16:68813382-68813382 + 996698 COSM19744 c.377_378insC p.P127fs*41 Insertion - Frameshift 16:68801883-68801884 + D-05 COSM4766189 c.2483_2484insT p.S829fs*6 Insertion - Frameshift 16:68833333-68833334 + S02194 COSM5674841 c.211C>G p.P71A Substitution - Missense 19:3526135-3526135 + 1001676 COSM20831 c.1137+?del? p.? Unknown 587228 COSM1200399 c.572G>A p.S191N Substitution - Missense 16:68808733-68808733 + 997761 COSM19801 c.1009-2A>C p.? Unknown 16:68812133-68812133 + BT1172 COSM19529 c.960_961ins? p.?fs Insertion - Frameshift 16:68811811-68811812 + TCGA-B9-5156-01 COSM3989929 c.501C>A p.P167P Substitution - coding silent 19:3527661-3527661 + 992999 COSM19508 c.274C>T p.H92Y Substitution - Missense 16:68801780-68801780 + TCGA-EE-A2MR-06 COSM3532357 c.447C>T p.S149S Substitution - coding silent 19:3527039-3527039 + MDA-MB-435 COSM1679221 c.568T>C p.Y190H Substitution - Missense 16:68808729-68808729 + 600MPE COSM20799 c.?_?del? p.? Unknown TCGA-A8-A0A6-01 COSM1379181 c.1565+1G>A p.? Unknown 16:68815760-68815760 + LUAD-S01405 COSM398950 c.1252G>A p.D418N Substitution - Missense 16:68813427-68813427 + TCGA-AO-A128-01 COSM1679223 c.2450C>T p.A817V Substitution - Missense 16:68833300-68833300 + TCGA-AH-6544-01 COSM1563542 c.1423G>A p.V475M Substitution - Missense 16:68815617-68815617 + T2197 COSM4670766 c.1422C>T p.T474T Substitution - coding silent 16:68815616-68815616 + pfg122T COSM4336503 c.1119delG p.G375fs*14 Deletion - Frameshift 19:3532527-3532527 + 999854 COSM20770 c.1105A>G p.N369D Substitution - Missense 16:68812231-68812231 + TCGA-G2-A2EL-01 COSM1302176 c.741G>A p.E247E Substitution - coding silent 16:68810250-68810250 + TCGA-AC-A2FO-01 COSM5833159 c.2469_2470insG p.A824fs*5 Insertion - Frameshift 16:68833319-68833320 + 1001677 COSM20775 c.2253C>T p.N751N Substitution - coding silent 16:68828262-68828262 + 2 COSM1659128 c.2467delA p.T823fs*23 Deletion - Frameshift 16:68833317-68833317 + 0065_CRUK_PC_0065_T1_DNA COSM4413706 c.163+4A>C p.? Unknown 16:68738415-68738415 + EWS502 COSM4579196 c.2643C>T p.D881D Substitution - coding silent 16:68833493-68833493 + NCI-H2122 COSM13114 c.493_510del18 p.E165_P170delENEKGP Deletion - In frame 16:68808529-68808546 + pfg136T COSM4747420 c.461_466delGAGACT p.D155_W156delDW Deletion - In frame 16:68808497-68808502 + SW48 COSM3197038 c.487_488insC p.R165fs*60 Insertion - Frameshift 19:3527647-3527648 + TCGA-F5-6811-01 COSM1563546 c.318C>T p.T106T Substitution - coding silent 16:68801824-68801824 + 996697 COSM19743 c.1849G>A p.A617T Substitution - Missense 16:68822138-68822138 + 12 COSM19785 c.786_794CACCCAGGA>T p.T263fs*3 Complex - frameshift 16:68810295-68810303 + CSCC-27-T COSM3818354 c.1921C>T p.Q641* Substitution - Nonsense 16:68822210-68822210 + TCGA-BH-A2L8-01 COSM5833158 c.2400delC p.P801fs*15 Deletion - Frameshift 16:68829758-68829758 + TCGA-BP-4977-01 COSM471990 c.2224C>T p.L742L Substitution - coding silent 16:68828233-68828233 + 41T COSM3712170 c.478C>T p.P160S Substitution - Missense 16:68808514-68808514 + 996991 COSM19759 c.781G>T p.E261* Substitution - Nonsense 16:68810290-68810290 + BT949 COSM19534 c.1693_1694ins? p.?fs Insertion - Frameshift 16:68819407-68819408 + SJMB002 COSM255866 c.187C>G p.R63G Substitution - Missense 16:68801693-68801693 + TCGA-JX-A3Q0-01 COSM4824743 c.2282G>A p.G761E Substitution - Missense 16:68828291-68828291 + 2492720 COSM5722784 c.699C>T p.T233T Substitution - coding silent 19:3530836-3530836 + TCGA-GM-A2DD-01 COSM3818345 c.752C>A p.T251K Substitution - Missense 16:68810261-68810261 + SCC-15 COSM308522 c.1214A>G p.N405S Substitution - Missense 16:68813389-68813389 + TCGA-B0-5692-01 COSM19485 c.944A>G p.N315S Substitution - Missense 16:68811795-68811795 + OCUB-F COSM19504 c.49_163del115 p.V17fs*1 Deletion - Frameshift 16:68738297-68738411 + pfg122T COSM3197047 c.1119delG p.G375fs*14 Deletion - Frameshift 19:3532527-3532527 + PD4194a COSM5774432 c.87C>G p.H29Q Substitution - Missense 16:68738335-68738335 + pfg023T COSM4756923 c.531+1G>A p.? Unknown 16:68808568-68808568 + BT850 COSM19537 c.1948_1964del17 p.I650fs*7 Deletion - Frameshift 16:68823410-68823426 + NYU872 COSM4770847 c.1984G>A p.D662N Substitution - Missense 16:68823446-68823446 + 996872 COSM19754 c.522_531+6del16 p.? Unknown 16:68808558-68808573 + 1001680 COSM20830 c.1320+1G>T p.? Unknown 16:68813496-68813496 + TCGA-CM-6171-01 COSM5160123 c.718C>T p.R240W Substitution - Missense 19:3530855-3530855 + 2492723 COSM5722784 c.699C>T p.T233T Substitution - coding silent 19:3530836-3530836 + PD18756a COSM435602 c.1531C>T p.Q511* Substitution - Nonsense 16:68815725-68815725 + TCGA-G3-A7M8-01 COSM4922541 c.1048C>T p.Q350* Substitution - Nonsense 19:3532456-3532456 + TCGA-BQ-7046-01 COSM3989928 c.120G>A p.S40S Substitution - coding silent 19:3525918-3525918 + TCGA-B6-A2IU-01 COSM3818342 c.583C>T p.Q195* Substitution - Nonsense 16:68808744-68808744 + PD9578a COSM5752496 c.163+1_163+2delGT p.? Unknown 16:68738412-68738413 + D-09 COSM4766211 c.755T>G p.V252G Substitution - Missense 16:68810264-68810264 + TCGA-RP-A694-06 COSM4894219 c.2602C>T p.R868C Substitution - Missense 16:68833452-68833452 + pfg136T COSM4756920 c.468G>T p.W156C Substitution - Missense 16:68808504-68808504 + SH-1362 COSM4129242 c.1896C>T p.H632H Substitution - coding silent 16:68822185-68822185 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.413123;Hs.413133 19p13.3 603619 2457397|CGAP|BC013413|C/T|coding|Phe469Phe|1595|Candidate; 2457398|CGAP|BC013413|A/G|non-coding||1678|Validated Hs.461085;Hs.461086 16q22.1 192090

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer AAGTCACGCTG - Frameshift p.V114Yfs*50 c.340_350delGTCACGCTGAA 16 68835747 BRCA - A Frameshift p.A401Dfs*2 c.1201_1202insA 16 68847279 BRCA A - Frameshift p.I505Sfs*17 c.1513delA 16 68849608 BRCA AGAACCTCGAACTATATTCTTCTGTG - Frameshift p.P597Efs*11 c.1788_1813delACCTCGAACTATATTCTTCTGTGAGA 16 68855977 BRCA A G Missense p.D290G c.869A>G 16 68845623 STAD A G Missense p.K113E c.337A>G 16 68835746 BLCA A G Missense p.K738R c.2213A>G 16 68862125 LUAD A G Missense p.M316V c.946A>G 16 68845700 OV A G Missense p.N315S c.944A>G 16 68845698 RCCC A G Missense p.N666S c.1997A>G 16 68857362 UCEC A G Missense p.N867S c.2600A>G 16 68867353 BRCA A G Missense p.R222G c.664A>G 16 68842728 STAD A G SpliceAcceptorSNV . c.688-2A>G 16 68844098 BRCA A G Synonymous p.P654P c.1962A>G 16 68857327 BRCA AGTCACT - Frameshift p.V365Tfs*26 c.1092_1098delAGTCACT 16 68846121 BRCA - AT Frameshift p.D756Efs*15 c.2267_2268insAT 16 68862179 BRCA ATGGCCT - Frameshift p.M656*fs*1 c.1966_1972delATGGCCT 16 68857331 BRCA A T Missense p.D400V c.1199A>T 16 68847277 STAD A T Missense p.D402V c.1205A>T 16 68847283 STAD A T Missense p.N606I c.1817A>T 16 68856009 UCEC A T Missense p.Q610L c.1829A>T 16 68856021 BRCA A T Nonsense p.K668* c.2002A>T 16 68857367 BRCA - CA Frameshift p.S19Tfs*38 c.54_55insAC 16 68772204 BRCA C A Missense p.A137E c.410C>A 16 68842349 HNSC C A Missense p.D569E c.1707C>A 16 68853324 HNSC C A Missense p.D858E c.2574C>A 16 68867327 HNSC C A Missense p.N558K c.1674C>A 16 68853291 HNSC C A Missense p.P260H c.779C>A 16 68844191 BRCA C A Missense p.Q195K c.583C>A 16 68842647 BRCA - CCC MultiAAMissense p.E167delinsDP c.500_501insCCC 16 68842439 BRCA C - Frameshift p.D308Ifs*48 c.922delG 16 68845676 BRCA C - Frameshift p.H128Ifs*87 c.382delC 16 68835788 BRCA C - Frameshift p.H128Ifs*87 c.382delC 16 68835788 STAD - C Frameshift p.I594Hfs*11 c.1779dupC 16 68855967 BRCA - C Frameshift p.P127Afs*41 c.377dupC 16 68835781 BRCA C - Frameshift p.P159Lfs*56 c.476delC 16 68842414 BRCA C - Frameshift p.P339Lfs*17 c.1016delC 16 68846043 BRCA - C Frameshift p.Q765Pfs*4 c.2293dupC 16 68862204 BRCA C - Frameshift p.Y508Tfs*14 c.1521delC 16 68849617 BRCA C G Missense p.L798V c.2392C>G 16 68863653 BLCA C G Missense p.R598G c.1792C>G 16 68855984 PRAD C G Missense p.T560R c.1679C>G 16 68853296 BRCA - CTGC Frameshift p.L582Pfs*7 c.1744_1745insCTGC 16 68855936 BRCA C T Missense p.A634V c.1901C>T 16 68856093 GBM C T Missense p.A735V c.2204C>T 16 68862116 SCLC C T Missense p.A824V c.2471C>T 16 68867224 UCEC C T Missense p.L71F c.211C>T 16 68835620 LUSC C T Missense p.P125L c.374C>T 16 68835783 CM C T Missense p.P277S c.829C>T 16 68844241 LUSC C T Missense p.P429L c.1286C>T 16 68847364 CM C T Missense p.P607S c.1819C>T 16 68856011 BRCA C T Missense p.P744S c.2230C>T 16 68862142 CM C T Missense p.P825L c.2474C>T 16 68867227 CM C T Missense p.R784C c.2350C>T 16 68863611 CM C T Missense p.S133F c.398C>T 16 68842337 BLCA C T Missense p.S543F c.1628C>T 16 68853245 CM C T Missense p.T379M c.1136C>T 16 68846165 PRAD C T Nonsense p.Q23* c.67C>T 16 68772218 BRCA C T Nonsense p.Q448* c.1342C>T 16 68849439 BRCA C T Nonsense p.Q503* c.1507C>T 16 68849604 BRCA C T Nonsense p.Q511* c.1531C>T 16 68849628 BRCA C T Nonsense p.R335* c.1003C>T 16 68845757 COREAD C T Nonsense p.R63* c.187C>T 16 68835596 BRCA C T Synonymous p.G760G c.2280C>T 16 68862192 STAD C T Synonymous p.L742L c.2224C>T 16 68862136 RCCC C T Synonymous p.N591N c.1773C>T 16 68855965 GBM C T Synonymous p.S70S c.210C>T 16 68835619 CM C T Synonymous p.V464V c.1392C>T 16 68849489 HNSC C T Synonymous p.V611V c.1833C>T 16 68856025 CM GAGGTCACAGCCACA - InFrameDeletion p.E283_T287delEVTAT c.849_863delGGTCACAGCCACAGA 16 68845601 BRCA GAGTC - Frameshift p.G324Dfs*24 c.971_975delGAGTC 16 68845725 BRCA G A IntronicSNV . c.1320+5G>A 16 68847403 STAD G A Missense p.A102T c.304G>A 16 68835713 STAD G A Missense p.A403T c.1207G>A 16 68847285 UCEC G A Missense p.D313N c.937G>A 16 68845691 BLCA G A Missense p.D552N c.1654G>A 16 68853271 BRCA G A Missense p.D644N c.1930G>A 16 68856122 BRCA G A Missense p.E138K c.412G>A 16 68842351 BRCA G A Missense p.E243K c.727G>A 16 68844139 BRCA G A Missense p.E336K c.1006G>A 16 68845760 STAD G A Missense p.E386K c.1156G>A 16 68847234 BLCA G A Missense p.E490K c.1468G>A 16 68849565 BRCA G A Missense p.E497K c.1489G>A 16 68849586 ESCA G A Missense p.E551K c.1651G>A 16 68853268 CM G A Missense p.G212E c.635G>A 16 68842699 STAD G A Missense p.R224H c.671G>A 16 68842735 HNSC G A Missense p.R732Q c.2195G>A 16 68862107 BRCA G A Missense p.R732Q c.2195G>A 16 68862107 UCEC G A Missense p.V694I c.2080G>A 16 68857445 STAD G A Nonsense p.W526* c.1578G>A 16 68853195 BRCA G A Nonsense p.W532* c.1596G>A 16 68853213 ESCA G A SpliceAcceptorSNV . c.688-1G>A 16 68844099 BRCA G A SpliceDonorSNV . c.1137+1G>A 16 68846167 BRCA G A SpliceDonorSNV . c.1936+1G>A 16 68856129 BRCA G A SpliceDonorSNV . c.832+1G>A 16 68844245 BRCA G A Synonymous p.A735A c.2205G>A 16 68862117 STAD G A Synonymous p.E247E c.741G>A 16 68844153 BLCA G A Synonymous p.E336E c.1008G>A 16 68845762 BRCA G A Synonymous p.R524R c.1572G>A 16 68853189 CM G A Synonymous p.T379T c.1137G>A 16 68846166 BRCA G A Synonymous p.T560T c.1680G>A 16 68853297 HNSC G A Synonymous p.T560T c.1680G>A 16 68853297 STAD GCCCAGAAAATGAAAAAG - InFrameDeletion p.E165_P170delENEKGP c.493_510delGAAAATGAAAAAGGCCCA 16 68842427 BRCA G C Missense p.E243Q c.727G>C 16 68844139 BLCA G C Missense p.E445Q c.1333G>C 16 68849430 LUSC G C SpliceAcceptorSNV . c.532-1G>C 16 68842595 PAAD GCT - InFrameDeletion p.L15delL c.44_46delTGC 16 68771348 CM G - Frameshift p.D291Mfs*3 c.871delG 16 68845625 BRCA G - Frameshift p.E283Rfs*11 c.847delG 16 68845600 BRCA G - Frameshift p.E518Nfs*4 c.1552delG 16 68849648 BRCA G - Frameshift p.G571Vfs*13 c.1711+1delG 16 68853328 UCEC G - Frameshift p.G759Efs*11 c.2276delG 16 68862187 BRCA - G Frameshift p.I161Hfs*7 c.479_480insG 16 68842418 BRCA GTCATGGAAG - Frameshift p.M272Lfs*7 c.813_822delCATGGAAGGT 16 68844223 BRCA G T Missense p.D254Y c.760G>T 16 68844172 STAD G T Missense p.D587Y c.1759G>T 16 68855951 ESCA G T Missense p.K440N c.1320G>T 16 68847398 STAD G T Missense p.Q129H c.387G>T 16 68835796 LUAD G T Missense p.R492I c.1475G>T 16 68849572 BRCA G T Missense p.V460L c.1378G>T 16 68849475 LUAD G T Missense p.W409L c.1226G>T 16 68847304 BRCA G T Nonsense p.E35* c.103G>T 16 68772254 BRCA G T Nonsense p.E494* c.1480G>T 16 68849577 BRCA G T Nonsense p.E781* c.2341G>T 16 68863602 BRCA G T SpliceAcceptorSNV . c.2165-1G>T 16 68862076 BRCA G T SpliceDonorSNV . c.1320+1G>T 16 68847399 STAD G T SpliceDonorSNV . c.1936+1G>T 16 68856129 BRCA G T SpliceDonorSNV . c.1936+1G>T 16 68856129 STAD TACCCCAGCGTGGGAGGCTG - Frameshift p.T406Ifs*6 c.1217_1236delCCCCAGCGTGGGAGGCTGTA 16 68847293 BRCA T A Missense p.V188D c.563T>A 16 68842627 STAD T A Missense p.V737D c.2210T>A 16 68862122 RCCC TC - Frameshift p.H233Rfs*10 c.696_697delTC 16 68844104 BRCA TCGTAA - InFrameDeletion p.V392_I393delVI c.1174_1179delGTAATC 16 68847250 HNSC - T Frameshift p.I650Yfs*13 c.1947dupT 16 68857312 BRCA T - Frameshift p.P708Lfs*14 c.2121delT 16 68857485 BRCA - T Frameshift p.T627Hfs*36 c.1877dupT 16 68856068 BRCA - T Frameshift p.T679Dfs*9 c.2033dupT 16 68857398 BRCA - TGAT Nonsense p.D828*fs*1 c.2481_2482insTGAT 16 68867234 BRCA TGCACCAACCCTCA - Frameshift p.A788Efs*14 c.2363_2376delCACCAACCCTCATG 16 68863622 BRCA T G Nonsense p.Y523* c.1569T>G 16 68853186 BRCA T G SpliceDonorSNV . c.687+2T>G 16 68842753 HNSC - T Nonsense p.D313*fs*1 c.932dupT 16 68845686 BRCA - T Nonsense p.E757*fs*1 c.2268dupT 16 68862180 BRCA A G Missense p.Q401R c.1202A>G 19 3532608 RCCC A T Missense p.Q350L c.1049A>T 19 3532455 HNSC C A Missense p.N84K c.252C>A 19 3526174 CM C A Missense p.P50H c.149C>A 19 3525945 LUAD C A Missense p.T233N c.698C>A 19 3530833 NB C A Synonymous p.S197S c.591C>A 19 3527749 CM C A Synonymous p.V427V c.1281C>A 19 3533330 RCCC CC TT Missense p.P182L c.545_546delinsTT 19 3527703 CM C - Frameshift p.T129Sfs*77 c.386delC 19 3526383 ESCA C G Missense p.P175A c.523C>G 19 3527681 PRAD C G Missense p.R445G c.1333C>G 19 3533382 HC C G Nonsense p.Y148* c.444C>G 19 3527034 STAD - C Nonsense p.D454*fs*1 c.1358dupC 19 3534426 NB CTGCT - Frameshift p.L94Qfs*3 c.281_285delTGCTC 19 3526277 UCEC C T Missense p.P431L c.1292C>T 19 3533341 LUAD C T Missense p.P50S c.148C>T 19 3525944 CM C T Missense p.R477C c.1429C>T 19 3534500 BLCA C T Missense p.S172F c.515C>T 19 3527673 CM C T Missense p.S196L c.587C>T 19 3527745 CM C T Missense p.S443F c.1328C>T 19 3533377 CM C T Synonymous p.I13I c.39C>T 19 3523026 CM C T Synonymous p.I174I c.522C>T 19 3527680 CM C T Synonymous p.T216T c.648C>T 19 3527806 CM C T Synonymous p.V427V c.1281C>T 19 3533330 CM G A Missense p.E183K c.547G>A 19 3527705 HNSC G A Missense p.E18K c.52G>A 19 3523039 THCA G A Missense p.G88S c.262G>A 19 3526259 HNSC G A Missense p.R496Q c.1487G>A 19 3534830 HNSC G A Missense p.V253M c.757G>A 19 3531748 RCCC G A Synonymous p.K429K c.1287G>A 19 3533336 RCCC G C Missense p.G376R c.1126G>C 19 3532532 LGG G C Missense p.Q16H c.48G>C 19 3523035 RCCC G C Missense p.W57C c.171G>C 19 3525967 STAD G C Synonymous p.L192L c.576G>C 19 3527734 ESCA G T Synonymous p.T417T c.1251G>T 19 3533300 STAD