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 3646276 3646276 + Missense_Mutation SNP G G A TCGA-OR-A5J6-01A-31D-A29I-10 TCGA-OR-A5J6-10A-01D-A29L-10 g.chr16:3646276G>A c.1802C>T c.(1801-1803)tCg>tTg p.S601L BLCA 16 3632361 3632361 + Silent SNP C C T TCGA-FD-A6TC-01A-21D-A339-08 TCGA-FD-A6TC-10A-21D-A339-08 g.chr16:3632361C>T c.5487G>A c.(5485-5487)aaG>aaA p.K1829K BLCA 16 3632493 3632493 + Silent SNP C C A TCGA-SY-A9G5-01A-11D-A38G-08 TCGA-SY-A9G5-10A-01D-A38J-08 g.chr16:3632493C>A c.5355G>T c.(5353-5355)ctG>ctT p.L1785L BLCA 16 3632496 3632496 + Silent SNP C C T TCGA-GV-A6ZA-01A-12D-A339-08 TCGA-GV-A6ZA-10A-01D-A339-08 g.chr16:3632496C>T c.5352G>A c.(5350-5352)gaG>gaA p.E1784E BLCA 16 3632546 3632546 + Missense_Mutation SNP G G C TCGA-XF-AAMX-01A-11D-A42E-08 TCGA-XF-AAMX-10A-01D-A42H-08 g.chr16:3632546G>C c.5302C>G c.(5302-5304)Cag>Gag p.Q1768E BLCA 16 3632618 3632618 + Nonsense_Mutation SNP G G A TCGA-ZF-AA4X-01A-11D-A38G-08 TCGA-ZF-AA4X-10A-01D-A38J-08 g.chr16:3632618G>A c.5230C>T c.(5230-5232)Cag>Tag p.Q1744* BLCA 16 3633236 3633236 + Missense_Mutation SNP T T C TCGA-K4-A3WV-01A-11D-A22Z-08 TCGA-K4-A3WV-10A-01D-A22Z-08 g.chr16:3633236T>C c.5015A>G c.(5014-5016)cAt>cGt p.H1672R BLCA 16 3639021 3639021 + Missense_Mutation SNP C C T TCGA-G2-AA3B-01A-11D-A391-08 TCGA-G2-AA3B-10A-01D-A394-08 g.chr16:3639021C>T c.4618G>A c.(4618-4620)Gaa>Aaa p.E1540K BLCA 16 3639472 3639472 + Silent SNP C C T TCGA-XF-AAMF-01A-21D-A42E-08 TCGA-XF-AAMF-10A-01D-A42H-08 g.chr16:3639472C>T c.4167G>A c.(4165-4167)gcG>gcA p.A1389A BLCA 16 3639936 3639936 + Missense_Mutation SNP G G A TCGA-XF-A9T5-01A-11D-A42E-08 TCGA-XF-A9T5-10A-01D-A42H-08 g.chr16:3639936G>A c.3703C>T c.(3703-3705)Ccc>Tcc p.P1235S BLCA 16 3639978 3639978 + Missense_Mutation SNP C C A TCGA-GV-A3QH-01A-11D-A21Z-08 TCGA-GV-A3QH-10A-01D-A21Z-08 g.chr16:3639978C>A c.3661G>T c.(3661-3663)Gcg>Tcg p.A1221S BLCA 16 3640038 3640038 + Missense_Mutation SNP G G C TCGA-4Z-AA86-01A-11D-A391-08 TCGA-4Z-AA86-10A-01D-A394-08 g.chr16:3640038G>C c.3601C>G c.(3601-3603)Cag>Gag p.Q1201E BLCA 16 3640180 3640180 + Silent SNP G G C TCGA-4Z-AA86-01A-11D-A391-08 TCGA-4Z-AA86-10A-01D-A394-08 g.chr16:3640180G>C c.3459C>G c.(3457-3459)ctC>ctG p.L1153L BLCA 16 3640211 3640211 + Missense_Mutation SNP G G A TCGA-DK-A1AC-01A-11D-A13W-08 TCGA-DK-A1AC-10A-01D-A13W-08 g.chr16:3640211G>A c.3428C>T c.(3427-3429)tCc>tTc p.S1143F BLCA 16 3640393 3640393 + Silent SNP C C T TCGA-DK-A6B6-01A-11D-A30E-08 TCGA-DK-A6B6-10A-01D-A30H-08 g.chr16:3640393C>T c.3246G>A c.(3244-3246)caG>caA p.Q1082Q BLCA 16 3640508 3640508 + Missense_Mutation SNP C C A TCGA-GU-A767-01A-11D-A32B-08 TCGA-GU-A767-10A-01D-A329-08 g.chr16:3640508C>A c.3131G>T c.(3130-3132)aGt>aTt p.S1044I BLCA 16 3640578 3640578 + Missense_Mutation SNP G G A TCGA-4Z-AA86-01A-11D-A391-08 TCGA-4Z-AA86-10A-01D-A394-08 g.chr16:3640578G>A c.3061C>T c.(3061-3063)Cgc>Tgc p.R1021C BLCA 16 3640581 3640581 + Missense_Mutation SNP G G C TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr16:3640581G>C c.3058C>G c.(3058-3060)Cat>Gat p.H1020D BLCA 16 3640791 3640791 + Missense_Mutation SNP C C G TCGA-FD-A3SS-01A-12D-A22Z-08 TCGA-FD-A3SS-10A-01D-A22Z-08 g.chr16:3640791C>G c.2848G>C c.(2848-2850)Gag>Cag p.E950Q BLCA 16 3640829 3640829 + Missense_Mutation SNP C C T TCGA-BL-A5ZZ-01A-31D-A30E-08 TCGA-BL-A5ZZ-10A-01D-A30H-08 g.chr16:3640829C>T c.2810G>A c.(2809-2811)gGg>gAg p.G937E BLCA 16 3640901 3640901 + Missense_Mutation SNP C C G TCGA-XF-A9SI-01A-11D-A391-08 TCGA-XF-A9SI-10A-01D-A394-08 g.chr16:3640901C>G c.2738G>C c.(2737-2739)aGa>aCa p.R913T BLCA 16 3641190 3641190 + Missense_Mutation SNP C C T TCGA-DK-A1AC-01A-11D-A13W-08 TCGA-DK-A1AC-10A-01D-A13W-08 g.chr16:3641190C>T c.2449G>A c.(2449-2451)Gaa>Aaa p.E817K BLCA 16 3642827 3642827 + Missense_Mutation SNP G G C TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr16:3642827G>C c.2200C>G c.(2200-2202)Ctg>Gtg p.L734V BLCA 16 3642839 3642839 + Missense_Mutation SNP C C G TCGA-FD-A62P-01A-32D-A30E-08 TCGA-FD-A62P-10A-01D-A30H-08 g.chr16:3642839C>G c.2188G>C c.(2188-2190)Gag>Cag p.E730Q BLCA 16 3656547 3656547 + Missense_Mutation SNP C C T TCGA-BT-A0YX-01A-11D-A10S-08 TCGA-BT-A0YX-10A-01D-A10S-08 g.chr16:3656547C>T c.688G>A c.(688-690)Gag>Aag p.E230K BLCA 16 3656571 3656571 + Missense_Mutation SNP C C T TCGA-YC-A8S6-01A-31D-A38G-08 TCGA-YC-A8S6-10A-01D-A38J-08 g.chr16:3656571C>T c.664G>A c.(664-666)Gag>Aag p.E222K BLCA 16 3658749 3658749 + Frame_Shift_Del DEL C C - TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr16:3658749delC c.217delG c.(217-219)gaafs p.E73fs BLCA 16 3658761 3658761 + Nonsense_Mutation SNP C C A TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr16:3658761C>A c.205G>T c.(205-207)Gaa>Taa p.E69* BLCA 16 3658957 3658957 + Silent SNP C C G TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr16:3658957C>G c.9G>C c.(7-9)ctG>ctC p.L3L BRCA 16 3632422 3632422 + Missense_Mutation SNP G G C TCGA-A7-A0DA-01A-31D-A10Y-09 TCGA-A7-A0DA-10A-01D-A110-09 g.chr16:3632422G>C c.5426C>G c.(5425-5427)aCc>aGc p.T1809S BRCA 16 3632522 3632523 + Frame_Shift_Ins INS - - G TCGA-A7-A0CJ-01A-21W-A019-09 TCGA-A7-A0CJ-10A-01W-A021-09 g.chr16:3632522_3632523insG c.5325_5326insC c.(5323-5328)ccctttfs p.F1776fs BRCA 16 3633370 3633370 + Missense_Mutation SNP C C G TCGA-E2-A10C-01A-21D-A10M-09 TCGA-E2-A10C-10A-01D-A10M-09 g.chr16:3633370C>G c.4881G>C c.(4879-4881)caG>caC p.Q1627H BRCA 16 3639839 3639839 + Missense_Mutation SNP C C T TCGA-A8-A09Z-01A-11W-A019-09 TCGA-A8-A09Z-10A-01W-A021-09 g.chr16:3639839C>T c.3800G>A c.(3799-3801)cGt>cAt p.R1267H BRCA 16 3640194 3640194 + Missense_Mutation SNP C C A TCGA-AR-A0U3-01A-11D-A10G-09 TCGA-AR-A0U3-10A-01D-A10G-09 g.chr16:3640194C>A c.3445G>T c.(3445-3447)Gat>Tat p.D1149Y BRCA 16 3641097 3641097 + Missense_Mutation SNP C C T TCGA-BH-A1F2-01A-31D-A13L-09 TCGA-BH-A1F2-11A-32D-A188-09 g.chr16:3641097C>T c.2542G>A c.(2542-2544)Gaa>Aaa p.E848K BRCA 16 3656563 3656563 + Missense_Mutation SNP C C A TCGA-E2-A1IJ-01A-11D-A142-09 TCGA-E2-A1IJ-10A-01D-A142-09 g.chr16:3656563C>A c.672G>T c.(670-672)ttG>ttT p.L224F BRCA 16 3658860 3658860 + Missense_Mutation SNP C C T TCGA-D8-A1J8-01A-11D-A13L-09 TCGA-D8-A1J8-10A-01D-A13O-09 g.chr16:3658860C>T c.106G>A c.(106-108)Gaa>Aaa p.E36K CESC 16 3632683 3632683 + Missense_Mutation SNP C C G TCGA-Q1-A5R1-01A-11D-A28B-09 TCGA-Q1-A5R1-10A-01D-A28E-09 g.chr16:3632683C>G c.5165G>C c.(5164-5166)tGt>tCt p.C1722S CESC 16 3639021 3639021 + Missense_Mutation SNP C C T TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr16:3639021C>T c.4618G>A c.(4618-4620)Gaa>Aaa p.E1540K CESC 16 3656621 3656621 + Missense_Mutation SNP G G A TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chr16:3656621G>A c.614C>T c.(613-615)aCa>aTa p.T205I CHOL 16 3640840 3640840 + Silent SNP G G T TCGA-W5-AA2Z-01A-11D-A417-09 TCGA-W5-AA2Z-11A-11D-A41A-09 g.chr16:3640840G>T c.2799C>A c.(2797-2799)ggC>ggA p.G933G CHOL 16 3656611 3656611 + Missense_Mutation SNP C C A TCGA-W5-AA39-01A-11D-A417-09 TCGA-W5-AA39-10A-01D-A41A-09 g.chr16:3656611C>A c.624G>T c.(622-624)ttG>ttT p.L208F COAD 16 3632466 3632466 + Silent SNP C C T TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr16:3632466C>T c.5382G>A c.(5380-5382)tcG>tcA p.S1794S COAD 16 3632640 3632640 + Silent SNP G G A TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr16:3632640G>A c.5208C>T c.(5206-5208)ggC>ggT p.G1736G COAD 16 3634824 3634824 + Missense_Mutation SNP G G A TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr16:3634824G>A c.4685C>T c.(4684-4686)cCg>cTg p.P1562L COAD 16 3639043 3639043 + Silent SNP G G A TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr16:3639043G>A c.4596C>T c.(4594-4596)agC>agT p.S1532S COAD 16 3639048 3639048 + Missense_Mutation SNP G G A TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr16:3639048G>A c.4591C>T c.(4591-4593)Cca>Tca p.P1531S COAD 16 3639109 3639109 + Silent SNP C C A TCGA-AZ-6608-01A-11D-1835-10 TCGA-AZ-6608-11A-01D-1835-10 g.chr16:3639109C>A c.4530G>T c.(4528-4530)ctG>ctT p.L1510L COAD 16 3639147 3639147 + Missense_Mutation SNP G G T TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr16:3639147G>T c.4492C>A c.(4492-4494)Ctg>Atg p.L1498M COAD 16 3639300 3639300 + Missense_Mutation SNP C C A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr16:3639300C>A c.4339G>T c.(4339-4341)Ggc>Tgc p.G1447C COAD 16 3639380 3639380 + Frame_Shift_Del DEL G G - TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr16:3639380delG c.4259delC c.(4258-4260)ccafs p.P1420fs COAD 16 3639398 3639398 + Frame_Shift_Del DEL G G - TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr16:3639398delG c.4241delC c.(4240-4242)ccafs p.P1414fs COAD 16 3639737 3639737 + Missense_Mutation SNP C C T TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr16:3639737C>T c.3902G>A c.(3901-3903)gGg>gAg p.G1301E COAD 16 3639799 3639799 + Silent SNP G G A TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr16:3639799G>A c.3840C>T c.(3838-3840)agC>agT p.S1280S COAD 16 3639827 3639827 + Missense_Mutation SNP G G A TCGA-AA-3660-01A-01D-1719-10 TCGA-AA-3660-11A-01D-1719-10 g.chr16:3639827G>A c.3812C>T c.(3811-3813)tCc>tTc p.S1271F COAD 16 3639918 3639918 + Missense_Mutation SNP G G A TCGA-F4-6809-01A-11D-1835-10 TCGA-F4-6809-10A-01D-1835-10 g.chr16:3639918G>A c.3721C>T c.(3721-3723)Cgt>Tgt p.R1241C COAD 16 3639963 3639963 + Missense_Mutation SNP G G A TCGA-CM-6674-01A-11D-1835-10 TCGA-CM-6674-10A-01D-1835-10 g.chr16:3639963G>A c.3676C>T c.(3676-3678)Cgg>Tgg p.R1226W COAD 16 3639972 3639972 + Missense_Mutation SNP G G A TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr16:3639972G>A c.3667C>T c.(3667-3669)Ccg>Tcg p.P1223S COAD 16 3639977 3639977 + Missense_Mutation SNP G G A TCGA-D5-6532-01A-11D-1719-10 TCGA-D5-6532-10A-01D-1719-10 g.chr16:3639977G>A c.3662C>T c.(3661-3663)gCg>gTg p.A1221V COAD 16 3640648 3640648 + Silent SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr16:3640648C>T c.2991G>A c.(2989-2991)ccG>ccA p.P997P COAD 16 3640733 3640733 + Missense_Mutation SNP C C A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr16:3640733C>A c.2906G>T c.(2905-2907)aGa>aTa p.R969I COAD 16 3640824 3640824 + Missense_Mutation SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr16:3640824G>A c.2815C>T c.(2815-2817)Cgg>Tgg p.R939W COAD 16 3641122 3641122 + Silent SNP G G A TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chr16:3641122G>A c.2517C>T c.(2515-2517)caC>caT p.H839H COAD 16 3641200 3641200 + Missense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr16:3641200C>A c.2439G>T c.(2437-2439)gaG>gaT p.E813D COAD 16 3641200 3641200 + Missense_Mutation SNP C C A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr16:3641200C>A c.2439G>T c.(2437-2439)gaG>gaT p.E813D COAD 16 3646191 3646191 + Silent SNP G G A TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr16:3646191G>A c.1887C>T c.(1885-1887)ccC>ccT p.P629P COAD 16 3646333 3646333 + Missense_Mutation SNP C C T TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr16:3646333C>T c.1745G>A c.(1744-1746)cGa>cAa p.R582Q COAD 16 3647390 3647390 + Missense_Mutation SNP C C T TCGA-G4-6310-01A-11D-1719-10 TCGA-G4-6310-10A-01D-1720-10 g.chr16:3647390C>T c.1673G>A c.(1672-1674)cGg>cAg p.R558Q COAD 16 3647433 3647433 + Missense_Mutation SNP C C A TCGA-D5-6537-01A-11D-1719-10 TCGA-D5-6537-10A-01D-1719-10 g.chr16:3647433C>A c.1630G>T c.(1630-1632)Gac>Tac p.D544Y COAD 16 3647605 3647605 + Silent SNP A A T TCGA-A6-3808-01A-01W-0995-10 TCGA-A6-3808-11A-01W-0995-10 g.chr16:3647605A>T c.1458T>A c.(1456-1458)cgT>cgA p.R486R COAD 16 3647829 3647829 + Missense_Mutation SNP A A C TCGA-AA-3527-01A-01W-0831-10 TCGA-AA-3527-10A-01W-0831-10 g.chr16:3647829A>C c.1335T>G c.(1333-1335)agT>agG p.S445R COAD 16 3647914 3647914 + Missense_Mutation SNP G G T TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr16:3647914G>T c.1250C>A c.(1249-1251)cCg>cAg p.P417Q COAD 16 3647922 3647922 + Silent SNP G G A TCGA-A6-4105-01A-02D-1771-10 TCGA-A6-4105-10A-01D-1771-10 g.chr16:3647922G>A c.1242C>T c.(1240-1242)gaC>gaT p.D414D COAD 16 3647923 3647923 + Missense_Mutation SNP T T C TCGA-G4-6306-01A-11D-1771-10 TCGA-G4-6306-10A-01D-1771-10 g.chr16:3647923T>C c.1241A>G c.(1240-1242)gAc>gGc p.D414G COAD 16 3647924 3647924 + Missense_Mutation SNP C C T TCGA-AY-5543-01A-01D-1650-10 TCGA-AY-5543-10A-01D-1650-10 g.chr16:3647924C>T c.1240G>A c.(1240-1242)Gac>Aac p.D414N COAD 16 3652148 3652148 + Silent SNP G G A TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr16:3652148G>A c.921C>T c.(919-921)aaC>aaT p.N307N COAD 16 3652148 3652148 + Silent SNP G G A TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr16:3652148G>A c.921C>T c.(919-921)aaC>aaT p.N307N COAD 16 3652216 3652216 + Missense_Mutation SNP C C A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr16:3652216C>A c.853G>T c.(853-855)Gat>Tat p.D285Y COAD 16 3656513 3656513 + Missense_Mutation SNP A A G TCGA-A6-5660-01A-01D-1650-10 TCGA-A6-5660-10A-01D-1650-10 g.chr16:3656513A>G c.722T>C c.(721-723)gTc>gCc p.V241A COAD 16 3656513 3656513 + Missense_Mutation SNP A A G TCGA-AD-6901-01A-11D-1924-10 TCGA-AD-6901-10A-01D-1924-10 g.chr16:3656513A>G c.722T>C c.(721-723)gTc>gCc p.V241A COAD 16 3656526 3656526 + Missense_Mutation SNP G G A TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr16:3656526G>A c.709C>T c.(709-711)Cgg>Tgg p.R237W COAD 16 3656682 3656682 + Missense_Mutation SNP C C A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr16:3656682C>A c.553G>T c.(553-555)Gac>Tac p.D185Y COAD 16 3658481 3658481 + Missense_Mutation SNP G G A TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr16:3658481G>A c.485C>T c.(484-486)aCg>aTg p.T162M COAD 16 3658568 3658568 + Missense_Mutation SNP G G A TCGA-AA-3821-01A-01W-0995-10 TCGA-AA-3821-10A-01W-0995-10 g.chr16:3658568G>A c.398C>T c.(397-399)cCg>cTg p.P133L COADREAD 16 3632466 3632466 + Silent SNP C C T TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr16:3632466C>T c.5382G>A c.(5380-5382)tcG>tcA p.S1794S COADREAD 16 3632513 3632513 + Missense_Mutation SNP G G A TCGA-DC-6160-01A-11D-1657-10 TCGA-DC-6160-10A-01D-1657-10 g.chr16:3632513G>A c.5335C>T c.(5335-5337)Cgg>Tgg p.R1779W COADREAD 16 3632640 3632640 + Silent SNP G G A TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr16:3632640G>A c.5208C>T c.(5206-5208)ggC>ggT p.G1736G COADREAD 16 3634824 3634824 + Missense_Mutation SNP G G A TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr16:3634824G>A c.4685C>T c.(4684-4686)cCg>cTg p.P1562L COADREAD 16 3639043 3639043 + Silent SNP G G A TCGA-CM-5861-01A-01D-1650-10 TCGA-CM-5861-10A-01D-1650-10 g.chr16:3639043G>A c.4596C>T c.(4594-4596)agC>agT p.S1532S COADREAD 16 3639048 3639048 + Missense_Mutation SNP G G A TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr16:3639048G>A c.4591C>T c.(4591-4593)Cca>Tca p.P1531S COADREAD 16 3639109 3639109 + Silent SNP C C A TCGA-AZ-6608-01A-11D-1835-10 TCGA-AZ-6608-11A-01D-1835-10 g.chr16:3639109C>A c.4530G>T c.(4528-4530)ctG>ctT p.L1510L COADREAD 16 3639147 3639147 + Missense_Mutation SNP G G T TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr16:3639147G>T c.4492C>A c.(4492-4494)Ctg>Atg p.L1498M COADREAD 16 3639300 3639300 + Missense_Mutation SNP C C A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr16:3639300C>A c.4339G>T c.(4339-4341)Ggc>Tgc p.G1447C COADREAD 16 3639380 3639380 + Frame_Shift_Del DEL G G - TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr16:3639380delG c.4259delC c.(4258-4260)ccafs p.P1420fs COADREAD 16 3639398 3639398 + Frame_Shift_Del DEL G G - TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr16:3639398delG c.4241delC c.(4240-4242)ccafs p.P1414fs COADREAD 16 3639737 3639737 + Missense_Mutation SNP C C T TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr16:3639737C>T c.3902G>A c.(3901-3903)gGg>gAg p.G1301E COADREAD 16 3639799 3639799 + Silent SNP G G A TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr16:3639799G>A c.3840C>T c.(3838-3840)agC>agT p.S1280S COADREAD 16 3639827 3639827 + Missense_Mutation SNP G G A TCGA-AA-3660-01A-01D-1719-10 TCGA-AA-3660-11A-01D-1719-10 g.chr16:3639827G>A c.3812C>T c.(3811-3813)tCc>tTc p.S1271F COADREAD 16 3639918 3639918 + Missense_Mutation SNP G G A TCGA-F4-6809-01A-11D-1835-10 TCGA-F4-6809-10A-01D-1835-10 g.chr16:3639918G>A c.3721C>T c.(3721-3723)Cgt>Tgt p.R1241C COADREAD 16 3639963 3639963 + Missense_Mutation SNP G G A TCGA-CM-6674-01A-11D-1835-10 TCGA-CM-6674-10A-01D-1835-10 g.chr16:3639963G>A c.3676C>T c.(3676-3678)Cgg>Tgg p.R1226W COADREAD 16 3639972 3639972 + Missense_Mutation SNP G G A TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr16:3639972G>A c.3667C>T c.(3667-3669)Ccg>Tcg p.P1223S COADREAD 16 3639977 3639977 + Missense_Mutation SNP G G A TCGA-D5-6532-01A-11D-1719-10 TCGA-D5-6532-10A-01D-1719-10 g.chr16:3639977G>A c.3662C>T c.(3661-3663)gCg>gTg p.A1221V COADREAD 16 3640008 3640008 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr16:3640008C>T c.3631G>A c.(3631-3633)Gaa>Aaa p.E1211K COADREAD 16 3640612 3640612 + Silent SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr16:3640612G>A c.3027C>T c.(3025-3027)ggC>ggT p.G1009G COADREAD 16 3640648 3640648 + Silent SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr16:3640648C>T c.2991G>A c.(2989-2991)ccG>ccA p.P997P COADREAD 16 3640733 3640733 + Missense_Mutation SNP C C A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr16:3640733C>A c.2906G>T c.(2905-2907)aGa>aTa p.R969I COADREAD 16 3640824 3640824 + Missense_Mutation SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr16:3640824G>A c.2815C>T c.(2815-2817)Cgg>Tgg p.R939W COADREAD 16 3641122 3641122 + Silent SNP G G A TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chr16:3641122G>A c.2517C>T c.(2515-2517)caC>caT p.H839H COADREAD 16 3641200 3641200 + Missense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr16:3641200C>A c.2439G>T c.(2437-2439)gaG>gaT p.E813D COADREAD 16 3641200 3641200 + Missense_Mutation SNP C C A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr16:3641200C>A c.2439G>T c.(2437-2439)gaG>gaT p.E813D COADREAD 16 3641293 3641293 + Silent SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr16:3641293G>A c.2346C>T c.(2344-2346)ctC>ctT p.L782L COADREAD 16 3646191 3646191 + Silent SNP G G A TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr16:3646191G>A c.1887C>T c.(1885-1887)ccC>ccT p.P629P COADREAD 16 3646333 3646333 + Missense_Mutation SNP C C T TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chr16:3646333C>T c.1745G>A c.(1744-1746)cGa>cAa p.R582Q COADREAD 16 3647390 3647390 + Missense_Mutation SNP C C T TCGA-G4-6310-01A-11D-1719-10 TCGA-G4-6310-10A-01D-1720-10 g.chr16:3647390C>T c.1673G>A c.(1672-1674)cGg>cAg p.R558Q COADREAD 16 3647433 3647433 + Missense_Mutation SNP C C A TCGA-D5-6537-01A-11D-1719-10 TCGA-D5-6537-10A-01D-1719-10 g.chr16:3647433C>A c.1630G>T c.(1630-1632)Gac>Tac p.D544Y COADREAD 16 3647605 3647605 + Silent SNP A A T TCGA-A6-3808-01A-01W-0995-10 TCGA-A6-3808-11A-01W-0995-10 g.chr16:3647605A>T c.1458T>A c.(1456-1458)cgT>cgA p.R486R COADREAD 16 3647829 3647829 + Missense_Mutation SNP A A C TCGA-AA-3527-01A-01W-0831-10 TCGA-AA-3527-10A-01W-0831-10 g.chr16:3647829A>C c.1335T>G c.(1333-1335)agT>agG p.S445R COADREAD 16 3647914 3647914 + Missense_Mutation SNP G G T TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr16:3647914G>T c.1250C>A c.(1249-1251)cCg>cAg p.P417Q COADREAD 16 3647922 3647922 + Silent SNP G G A TCGA-A6-4105-01A-02D-1771-10 TCGA-A6-4105-10A-01D-1771-10 g.chr16:3647922G>A c.1242C>T c.(1240-1242)gaC>gaT p.D414D COADREAD 16 3647923 3647923 + Missense_Mutation SNP T T C TCGA-G4-6306-01A-11D-1771-10 TCGA-G4-6306-10A-01D-1771-10 g.chr16:3647923T>C c.1241A>G c.(1240-1242)gAc>gGc p.D414G COADREAD 16 3647924 3647924 + Missense_Mutation SNP C C T TCGA-AG-3732-01A-11D-1657-10 TCGA-AG-3732-11A-01D-1657-10 g.chr16:3647924C>T c.1240G>A c.(1240-1242)Gac>Aac p.D414N COADREAD 16 3647924 3647924 + Missense_Mutation SNP C C T TCGA-AY-5543-01A-01D-1650-10 TCGA-AY-5543-10A-01D-1650-10 g.chr16:3647924C>T c.1240G>A c.(1240-1242)Gac>Aac p.D414N COADREAD 16 3652140 3652140 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr16:3652140C>T c.929G>A c.(928-930)cGa>cAa p.R310Q COADREAD 16 3652148 3652148 + Silent SNP G G A TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr16:3652148G>A c.921C>T c.(919-921)aaC>aaT p.N307N COADREAD 16 3652148 3652148 + Silent SNP G G A TCGA-A6-6780-01A-11D-1835-10 TCGA-A6-6780-10A-01D-1835-10 g.chr16:3652148G>A c.921C>T c.(919-921)aaC>aaT p.N307N COADREAD 16 3652216 3652216 + Missense_Mutation SNP C C A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr16:3652216C>A c.853G>T c.(853-855)Gat>Tat p.D285Y COADREAD 16 3656513 3656513 + Missense_Mutation SNP A A G TCGA-A6-5660-01A-01D-1650-10 TCGA-A6-5660-10A-01D-1650-10 g.chr16:3656513A>G c.722T>C c.(721-723)gTc>gCc p.V241A COADREAD 16 3656513 3656513 + Missense_Mutation SNP A A G TCGA-AD-6901-01A-11D-1924-10 TCGA-AD-6901-10A-01D-1924-10 g.chr16:3656513A>G c.722T>C c.(721-723)gTc>gCc p.V241A COADREAD 16 3656526 3656526 + Missense_Mutation SNP G G A TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr16:3656526G>A c.709C>T c.(709-711)Cgg>Tgg p.R237W COADREAD 16 3656682 3656682 + Missense_Mutation SNP C C A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr16:3656682C>A c.553G>T c.(553-555)Gac>Tac p.D185Y COADREAD 16 3658481 3658481 + Missense_Mutation SNP G G A TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr16:3658481G>A c.485C>T c.(484-486)aCg>aTg p.T162M COADREAD 16 3658568 3658568 + Missense_Mutation SNP G G A TCGA-AA-3821-01A-01W-0995-10 TCGA-AA-3821-10A-01W-0995-10 g.chr16:3658568G>A c.398C>T c.(397-399)cCg>cTg p.P133L DLBC 16 3633415 3633415 + Missense_Mutation SNP G G T TCGA-GR-A4D5-01A-11D-A31X-10 TCGA-GR-A4D5-10A-01D-A31X-10 g.chr16:3633415G>T c.4836C>A c.(4834-4836)gaC>gaA p.D1612E DLBC 16 3640893 3640893 + Missense_Mutation SNP C C A TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr16:3640893C>A c.2746G>T c.(2746-2748)Gcc>Tcc p.A916S DLBC 16 3656645 3656645 + Missense_Mutation SNP A A G TCGA-G8-6906-01A-11D-2210-10 TCGA-G8-6906-14A-01D-2210-10 g.chr16:3656645A>G c.590T>C c.(589-591)gTg>gCg p.V197A ESCA 16 3633194 3633194 + Missense_Mutation SNP G G T TCGA-X8-AAAR-01A-11D-A403-09 TCGA-X8-AAAR-10A-01D-A403-09 g.chr16:3633194G>T c.5057C>A c.(5056-5058)gCa>gAa p.A1686E ESCA 16 3633275 3633275 + Missense_Mutation SNP G G T TCGA-L5-A4OE-01A-11D-A27G-09 TCGA-L5-A4OE-11A-11D-A27G-09 g.chr16:3633275G>T c.4976C>A c.(4975-4977)cCt>cAt p.P1659H ESCA 16 3640930 3640930 + Silent SNP C C A TCGA-LN-A9FP-01A-31D-A387-09 TCGA-LN-A9FP-10A-01D-A38A-09 g.chr16:3640930C>A c.2709G>T c.(2707-2709)gtG>gtT p.V903V ESCA 16 3642792 3642792 + Silent SNP G G T TCGA-2H-A9GR-01A-12D-A37C-09 TCGA-2H-A9GR-11A-11D-A37F-09 g.chr16:3642792G>T c.2235C>A c.(2233-2235)acC>acA p.T745T ESCA 16 3647636 3647636 + Missense_Mutation SNP G G T TCGA-KH-A6WC-01A-11D-A33E-09 TCGA-KH-A6WC-10B-01D-A33H-09 g.chr16:3647636G>T c.1427C>A c.(1426-1428)tCt>tAt p.S476Y ESCA 16 3652151 3652151 + Missense_Mutation SNP C C T TCGA-IG-A3QL-01A-11D-A247-09 TCGA-IG-A3QL-10A-01D-A247-09 g.chr16:3652151C>T c.918G>A c.(916-918)atG>atA p.M306I ESCA 16 3656556 3656556 + Missense_Mutation SNP C C T TCGA-IG-A8O2-01A-11D-A36J-09 TCGA-IG-A8O2-10A-01D-A36M-09 g.chr16:3656556C>T c.679G>A c.(679-681)Gct>Act p.A227T GBM 16 3642834 3642834 + Silent SNP G G A TCGA-06-0122-01A-01D-1490-08 TCGA-06-0122-10A-01D-1490-08 g.chr16:3642834G>A c.2193C>T c.(2191-2193)gaC>gaT p.D731D GBM 16 3658781 3658781 + Missense_Mutation SNP A A G TCGA-74-6575-01A-11D-1845-08 TCGA-74-6575-10A-01D-1845-08 g.chr16:3658781A>G c.185T>C c.(184-186)gTg>gCg p.V62A GBMLGG 16 3632419 3632419 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:3632419G>T c.5429C>A c.(5428-5430)aCt>aAt p.T1810N GBMLGG 16 3632640 3632640 + Silent SNP G G A TCGA-WY-A859-01A-12D-A36O-08 TCGA-WY-A859-10A-01D-A367-08 g.chr16:3632640G>A c.5208C>T c.(5206-5208)ggC>ggT p.G1736G GBMLGG 16 3639670 3639670 + Silent SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:3639670T>C c.3969A>G c.(3967-3969)tcA>tcG p.S1323S GBMLGG 16 3640627 3640627 + Silent SNP G G A TCGA-HT-A5RB-01A-11D-A289-08 TCGA-HT-A5RB-10A-01D-A289-08 g.chr16:3640627G>A c.3012C>T c.(3010-3012)ccC>ccT p.P1004P GBMLGG 16 3640690 3640690 + Silent SNP G G A TCGA-DH-5140-01A-01D-1468-08 TCGA-DH-5140-10A-01D-1468-08 g.chr16:3640690G>A c.2949C>T c.(2947-2949)taC>taT p.Y983Y GBMLGG 16 3642834 3642834 + Silent SNP G G A TCGA-06-0122-01A-01D-1490-08 TCGA-06-0122-10A-01D-1490-08 g.chr16:3642834G>A c.2193C>T c.(2191-2193)gaC>gaT p.D731D GBMLGG 16 3645675 3645675 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:3645675G>A c.1944C>T c.(1942-1944)ggC>ggT p.G648G GBMLGG 16 3658781 3658781 + Missense_Mutation SNP A A G TCGA-74-6575-01A-11D-1845-08 TCGA-74-6575-10A-01D-1845-08 g.chr16:3658781A>G c.185T>C c.(184-186)gTg>gCg p.V62A HNSC 16 3632371 3632371 + Missense_Mutation SNP C C T TCGA-P3-A5Q5-01A-11D-A28R-08 TCGA-P3-A5Q5-10A-01D-A28U-08 g.chr16:3632371C>T c.5477G>A c.(5476-5478)cGg>cAg p.R1826Q HNSC 16 3632510 3632510 + Missense_Mutation SNP C C T TCGA-CQ-5326-01A-01D-1870-08 TCGA-CQ-5326-10A-01D-1870-08 g.chr16:3632510C>T c.5338G>A c.(5338-5340)Gag>Aag p.E1780K HNSC 16 3633428 3633428 + Missense_Mutation SNP G G A TCGA-CR-7388-01A-11D-2012-08 TCGA-CR-7388-10A-01D-2013-08 g.chr16:3633428G>A c.4823C>T c.(4822-4824)tCa>tTa p.S1608L HNSC 16 3639181 3639181 + Silent SNP C C T TCGA-CN-A642-01A-12D-A30E-08 TCGA-CN-A642-10A-01D-A30H-08 g.chr16:3639181C>T c.4458G>A c.(4456-4458)agG>agA p.R1486R HNSC 16 3639184 3639184 + Silent SNP C C T TCGA-CV-7099-01A-41D-2012-08 TCGA-CV-7099-10A-01D-2013-08 g.chr16:3639184C>T c.4455G>A c.(4453-4455)caG>caA p.Q1485Q HNSC 16 3639210 3639210 + Missense_Mutation SNP G G A TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr16:3639210G>A c.4429C>T c.(4429-4431)Ccc>Tcc p.P1477S HNSC 16 3639417 3639417 + Nonsense_Mutation SNP G G A TCGA-CR-6480-01A-11D-1870-08 TCGA-CR-6480-10A-01D-1870-08 g.chr16:3639417G>A c.4222C>T c.(4222-4224)Cag>Tag p.Q1408* HNSC 16 3639432 3639432 + Missense_Mutation SNP C C G TCGA-BA-A6DJ-01A-11D-A30E-08 TCGA-BA-A6DJ-10A-01D-A30H-08 g.chr16:3639432C>G c.4207G>C c.(4207-4209)Gag>Cag p.E1403Q HNSC 16 3641259 3641259 + Missense_Mutation SNP C C T TCGA-TN-A7HL-01A-11D-A34J-08 TCGA-TN-A7HL-10A-01D-A34M-08 g.chr16:3641259C>T c.2380G>A c.(2380-2382)Gac>Aac p.D794N HNSC 16 3645643 3645643 + Missense_Mutation SNP G G A TCGA-DQ-7591-01A-11D-2078-08 TCGA-DQ-7591-10A-01D-2078-08 g.chr16:3645643G>A c.1976C>T c.(1975-1977)tCg>tTg p.S659L HNSC 16 3646278 3646278 + Silent SNP C C T TCGA-CR-7379-01A-11D-2012-08 TCGA-CR-7379-10A-01D-2013-08 g.chr16:3646278C>T c.1800G>A c.(1798-1800)ccG>ccA p.P600P HNSC 16 3656527 3656527 + Silent SNP C C T TCGA-CV-7414-01A-11D-2078-08 TCGA-CV-7414-10A-01D-2078-08 g.chr16:3656527C>T c.708G>A c.(706-708)gcG>gcA p.A236A HNSC 16 3656656 3656656 + Missense_Mutation SNP C C G TCGA-CV-6942-01A-21D-2012-08 TCGA-CV-6942-10A-01D-2013-08 g.chr16:3656656C>G c.579G>C c.(577-579)ttG>ttC p.L193F KIPAN 16 3639200 3639200 + Missense_Mutation SNP C C T TCGA-B8-4621-01A-01D-1501-10 TCGA-B8-4621-10A-01D-1501-10 g.chr16:3639200C>T c.4439G>A c.(4438-4440)gGa>gAa p.G1480E KIPAN 16 3640657 3640657 + Silent SNP G G T TCGA-B0-5092-01A-01D-1421-08 TCGA-B0-5092-11A-01D-1421-08 g.chr16:3640657G>T c.2982C>A c.(2980-2982)atC>atA p.I994I KIPAN 16 3641170 3641170 + Nonsense_Mutation SNP C C T TCGA-CJ-5676-01A-11D-1534-10 TCGA-CJ-5676-11A-01D-1534-10 g.chr16:3641170C>T c.2469G>A c.(2467-2469)tgG>tgA p.W823* KIPAN 16 3641173 3641173 + Missense_Mutation SNP C C G TCGA-B3-3925-01A-01D-1458-08 TCGA-B3-3925-10A-01D-1458-08 g.chr16:3641173C>G c.2466G>C c.(2464-2466)atG>atC p.M822I KIPAN 16 3645657 3645657 + Frame_Shift_Del DEL C C - TCGA-HE-A5NH-01A-11D-A26P-10 TCGA-HE-A5NH-10A-01D-A26P-10 g.chr16:3645657delC c.1962delG c.(1960-1962)gggfs p.G654fs KIPAN 16 3652234 3652234 + Missense_Mutation SNP C C T TCGA-B0-4814-01A-01D-1361-10 TCGA-B0-4814-11A-01D-1361-10 g.chr16:3652234C>T c.835G>A c.(835-837)Gta>Ata p.V279I KIPAN 16 3656681 3656681 + Missense_Mutation SNP T T G TCGA-2Z-A9J8-01A-11D-A42J-10 TCGA-2Z-A9J8-10A-01D-A42M-10 g.chr16:3656681T>G c.554A>C c.(553-555)gAc>gCc p.D185A KIPAN 16 3658538 3658538 + Missense_Mutation SNP A A T TCGA-EU-5904-01A-11D-1669-08 TCGA-EU-5904-10A-01D-1669-08 g.chr16:3658538A>T c.428T>A c.(427-429)gTg>gAg p.V143E KIRC 16 3639200 3639200 + Missense_Mutation SNP C C T TCGA-B8-4621-01A-01D-1501-10 TCGA-B8-4621-10A-01D-1501-10 g.chr16:3639200C>T c.4439G>A c.(4438-4440)gGa>gAa p.G1480E KIRC 16 3640657 3640657 + Silent SNP G G T TCGA-B0-5092-01A-01D-1421-08 TCGA-B0-5092-11A-01D-1421-08 g.chr16:3640657G>T c.2982C>A c.(2980-2982)atC>atA p.I994I KIRC 16 3641170 3641170 + Nonsense_Mutation SNP C C T TCGA-CJ-5676-01A-11D-1534-10 TCGA-CJ-5676-11A-01D-1534-10 g.chr16:3641170C>T c.2469G>A c.(2467-2469)tgG>tgA p.W823* KIRC 16 3652234 3652234 + Missense_Mutation SNP C C T TCGA-B0-4814-01A-01D-1361-10 TCGA-B0-4814-11A-01D-1361-10 g.chr16:3652234C>T c.835G>A c.(835-837)Gta>Ata p.V279I KIRC 16 3658538 3658538 + Missense_Mutation SNP A A T TCGA-EU-5904-01A-11D-1669-08 TCGA-EU-5904-10A-01D-1669-08 g.chr16:3658538A>T c.428T>A c.(427-429)gTg>gAg p.V143E KIRP 16 3641173 3641173 + Missense_Mutation SNP C C G TCGA-B3-3925-01A-01D-1458-08 TCGA-B3-3925-10A-01D-1458-08 g.chr16:3641173C>G c.2466G>C c.(2464-2466)atG>atC p.M822I KIRP 16 3645657 3645657 + Frame_Shift_Del DEL C C - TCGA-HE-A5NH-01A-11D-A26P-10 TCGA-HE-A5NH-10A-01D-A26P-10 g.chr16:3645657delC c.1962delG c.(1960-1962)gggfs p.G654fs KIRP 16 3656681 3656681 + Missense_Mutation SNP T T G TCGA-2Z-A9J8-01A-11D-A42J-10 TCGA-2Z-A9J8-10A-01D-A42M-10 g.chr16:3656681T>G c.554A>C c.(553-555)gAc>gCc p.D185A LGG 16 3632419 3632419 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:3632419G>T c.5429C>A c.(5428-5430)aCt>aAt p.T1810N LGG 16 3632640 3632640 + Silent SNP G G A TCGA-WY-A859-01A-12D-A36O-08 TCGA-WY-A859-10A-01D-A367-08 g.chr16:3632640G>A c.5208C>T c.(5206-5208)ggC>ggT p.G1736G LGG 16 3639670 3639670 + Silent SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:3639670T>C c.3969A>G c.(3967-3969)tcA>tcG p.S1323S LGG 16 3640627 3640627 + Silent SNP G G A TCGA-HT-A5RB-01A-11D-A289-08 TCGA-HT-A5RB-10A-01D-A289-08 g.chr16:3640627G>A c.3012C>T c.(3010-3012)ccC>ccT p.P1004P LGG 16 3640690 3640690 + Silent SNP G G A TCGA-DH-5140-01A-01D-1468-08 TCGA-DH-5140-10A-01D-1468-08 g.chr16:3640690G>A c.2949C>T c.(2947-2949)taC>taT p.Y983Y LGG 16 3645675 3645675 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:3645675G>A c.1944C>T c.(1942-1944)ggC>ggT p.G648G LIHC 16 3633142 3633142 + Silent SNP C C T TCGA-DD-AAEE-01A-11D-A40R-10 TCGA-DD-AAEE-10A-01D-A40U-10 g.chr16:3633142C>T c.5109G>A c.(5107-5109)gtG>gtA p.V1703V LIHC 16 3634809 3634809 + Missense_Mutation SNP G G C TCGA-DD-AACQ-01A-11D-A40R-10 TCGA-DD-AACQ-10A-01D-A40U-10 g.chr16:3634809G>C c.4700C>G c.(4699-4701)tCc>tGc p.S1567C LIHC 16 3641076 3641076 + Missense_Mutation SNP A A C TCGA-K7-AAU7-01A-11D-A382-10 TCGA-K7-AAU7-10A-01D-A385-10 g.chr16:3641076A>C c.2563T>G c.(2563-2565)Tat>Gat p.Y855D LIHC 16 3642739 3642739 + Missense_Mutation SNP G G T TCGA-BW-A5NP-01A-11D-A27I-10 TCGA-BW-A5NP-10A-01D-A27I-10 g.chr16:3642739G>T c.2288C>A c.(2287-2289)cCt>cAt p.P763H LIHC 16 3647563 3647563 + Silent SNP C C A TCGA-DD-AAW2-01A-11D-A40P-10 TCGA-DD-AAW2-10A-01D-A40P-10 g.chr16:3647563C>A c.1500G>T c.(1498-1500)acG>acT p.T500T LIHC 16 3651153 3651153 + Silent SNP C C A TCGA-DD-A116-01A-11D-A12Z-10 TCGA-DD-A116-10A-01D-A12Z-10 g.chr16:3651153C>A c.990G>T c.(988-990)gtG>gtT p.V330V LIHC 16 3658812 3658812 + Missense_Mutation SNP T T C TCGA-2Y-A9GU-01A-11D-A382-10 TCGA-2Y-A9GU-10A-01D-A385-10 g.chr16:3658812T>C c.154A>G c.(154-156)Aaa>Gaa p.K52E LUAD 16 3632493 3632493 + Silent SNP C C T TCGA-55-A4DF-01A-11D-A24D-08 TCGA-55-A4DF-10A-01D-A24F-08 g.chr16:3632493C>T c.5355G>A c.(5353-5355)ctG>ctA p.L1785L LUAD 16 3632513 3632513 + Missense_Mutation SNP G G A TCGA-55-8204-01A-11D-2238-08 TCGA-55-8204-10A-01D-2238-08 g.chr16:3632513G>A c.5335C>T c.(5335-5337)Cgg>Tgg p.R1779W LUAD 16 3632583 3632583 + Silent SNP C C A TCGA-05-4382-01A-01D-1931-08 TCGA-05-4382-10A-01D-1265-08 g.chr16:3632583C>A c.5265G>T c.(5263-5265)gcG>gcT p.A1755A LUAD 16 3634823 3634823 + Silent SNP C C T TCGA-86-7711-01A-11D-2063-08 TCGA-86-7711-10A-01D-2063-08 g.chr16:3634823C>T c.4686G>A c.(4684-4686)ccG>ccA p.P1562P LUAD 16 3634838 3634838 + Missense_Mutation SNP T T G TCGA-78-7150-01A-21D-2036-08 TCGA-78-7150-10A-01D-2036-08 g.chr16:3634838T>G c.4671A>C c.(4669-4671)aaA>aaC p.K1557N LUAD 16 3634841 3634841 + Frame_Shift_Del DEL G G - TCGA-05-4244-01A-01D-1105-08 TCGA-05-4244-10A-01D-1105-08 g.chr16:3634841delG c.4668delC c.(4666-4668)cccfs p.P1556fs LUAD 16 3639153 3639153 + Missense_Mutation SNP C C A TCGA-86-8054-01A-11D-2238-08 TCGA-86-8054-10A-01D-2238-08 g.chr16:3639153C>A c.4486G>T c.(4486-4488)Ggc>Tgc p.G1496C LUAD 16 3639305 3639305 + Missense_Mutation SNP C C A TCGA-55-7913-01B-11D-2238-08 TCGA-55-7913-10A-01D-2238-08 g.chr16:3639305C>A c.4334G>T c.(4333-4335)cGg>cTg p.R1445L LUAD 16 3640014 3640014 + Missense_Mutation SNP T T C TCGA-44-A4SS-01A-11D-A24P-08 TCGA-44-A4SS-10A-01D-A24P-08 g.chr16:3640014T>C c.3625A>G c.(3625-3627)Aga>Gga p.R1209G LUAD 16 3640068 3640068 + Silent SNP G G A TCGA-O1-A52J-01A-11D-A25L-08 TCGA-O1-A52J-10A-01D-A25L-08 g.chr16:3640068G>A c.3571C>T c.(3571-3573)Ctg>Ttg p.L1191L LUAD 16 3640110 3640110 + Nonsense_Mutation SNP C C A TCGA-05-5425-01A-02D-1625-08 TCGA-05-5425-10A-01D-1625-08 g.chr16:3640110C>A c.3529G>T c.(3529-3531)Gaa>Taa p.E1177* LUAD 16 3640560 3640560 + Missense_Mutation SNP C C T TCGA-86-A4JF-01A-11D-A24P-08 TCGA-86-A4JF-10A-01D-A24P-08 g.chr16:3640560C>T c.3079G>A c.(3079-3081)Gca>Aca p.A1027T LUAD 16 3640876 3640876 + Silent SNP C C T TCGA-86-A4JF-01A-11D-A24P-08 TCGA-86-A4JF-10A-01D-A24P-08 g.chr16:3640876C>T c.2763G>A c.(2761-2763)gaG>gaA p.E921E LUAD 16 3642820 3642820 + Missense_Mutation SNP T T A TCGA-44-7667-01A-31D-2063-08 TCGA-44-7667-10A-01D-2063-08 g.chr16:3642820T>A c.2207A>T c.(2206-2208)cAg>cTg p.Q736L LUAD 16 3644562 3644562 + Missense_Mutation SNP C C T TCGA-55-8092-01A-11D-2238-08 TCGA-55-8092-10A-01D-2238-08 g.chr16:3644562C>T c.2052G>A c.(2050-2052)atG>atA p.M684I LUAD 16 3645675 3645675 + Silent SNP G G A TCGA-69-A59K-01A-11D-A25L-08 TCGA-69-A59K-10A-01D-A25L-08 g.chr16:3645675G>A c.1944C>T c.(1942-1944)ggC>ggT p.G648G LUAD 16 3647557 3647557 + Silent SNP T T C TCGA-75-5147-01A-01D-1625-08 TCGA-75-5147-10A-01D-1625-08 g.chr16:3647557T>C c.1506A>G c.(1504-1506)ccA>ccG p.P502P LUAD 16 3647809 3647809 + Missense_Mutation SNP C C A TCGA-MN-A4N5-01A-11D-A24P-08 TCGA-MN-A4N5-10A-01D-A24P-08 g.chr16:3647809C>A c.1355G>T c.(1354-1356)aGa>aTa p.R452I LUAD 16 3658545 3658545 + Missense_Mutation SNP C C A TCGA-17-Z022-01A-01W-0746-08 TCGA-17-Z022-11A-01W-0746-08 g.chr16:3658545C>A c.421G>T c.(421-423)Ggg>Tgg p.G141W LUSC 16 3633150 3633150 + Missense_Mutation SNP C C G TCGA-39-5031-01A-01D-1441-08 TCGA-39-5031-11A-01D-1441-08 g.chr16:3633150C>G c.5101G>C c.(5101-5103)Gaa>Caa p.E1701Q LUSC 16 3633448 3633448 + Nonsense_Mutation SNP G G T TCGA-37-3789-01A-01D-0983-08 TCGA-37-3789-10A-01D-0983-08 g.chr16:3633448G>T c.4803C>A c.(4801-4803)taC>taA p.Y1601* LUSC 16 3639381 3639381 + Missense_Mutation SNP G G A TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr16:3639381G>A c.4258C>T c.(4258-4260)Cca>Tca p.P1420S LUSC 16 3640826 3640826 + Missense_Mutation SNP G G T TCGA-22-5472-01A-01D-1632-08 TCGA-22-5472-11A-11D-1632-08 g.chr16:3640826G>T c.2813C>A c.(2812-2814)gCa>gAa p.A938E LUSC 16 3641118 3641118 + Missense_Mutation SNP C C G TCGA-22-5473-01A-01D-1632-08 TCGA-22-5473-11A-11D-1632-08 g.chr16:3641118C>G c.2521G>C c.(2521-2523)Gaa>Caa p.E841Q LUSC 16 3641121 3641121 + Missense_Mutation SNP C C G TCGA-21-1081-01A-01D-1521-08 TCGA-21-1081-10B-01D-1521-08 g.chr16:3641121C>G c.2518G>C c.(2518-2520)Gaa>Caa p.E840Q LUSC 16 3652259 3652259 + Missense_Mutation SNP C C G TCGA-33-4547-01A-01D-1267-08 TCGA-33-4547-11A-01D-1267-08 g.chr16:3652259C>G c.810G>C c.(808-810)ttG>ttC p.L270F LUSC 16 3656624 3656624 + Missense_Mutation SNP C C T TCGA-60-2722-01A-01D-1522-08 TCGA-60-2722-11A-01D-1522-08 g.chr16:3656624C>T c.611G>A c.(610-612)cGc>cAc p.R204H LUSC 16 3658448 3658448 + Missense_Mutation SNP G G C TCGA-22-5482-01A-01D-1632-08 TCGA-22-5482-11A-01D-1632-08 g.chr16:3658448G>C c.518C>G c.(517-519)tCc>tGc p.S173C LUSC 16 3658604 3658604 + Missense_Mutation SNP T T C TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr16:3658604T>C c.362A>G c.(361-363)aAa>aGa p.K121R LUSC 16 3658855 3658855 + Missense_Mutation SNP G G T TCGA-39-5035-01A-01D-1441-08 TCGA-39-5035-11A-01D-1441-08 g.chr16:3658855G>T c.111C>A c.(109-111)agC>agA p.S37R OV 16 3639355 3639355 + Missense_Mutation SNP C C A TCGA-24-1470-01A-01W-0553-09 TCGA-24-1470-10A-01W-0553-09 g.chr16:3639355C>A c.4284G>T c.(4282-4284)tgG>tgT p.W1428C OV 16 3639412 3639412 + Silent SNP G G C TCGA-61-1910-01A-01W-0639-09 TCGA-61-1910-11A-01W-0640-09 g.chr16:3639412G>C c.4227C>G c.(4225-4227)gcC>gcG p.A1409A OV 16 3639991 3639991 + Missense_Mutation SNP C C G TCGA-30-1718-01A-01W-0633-09 TCGA-30-1718-10A-01W-0633-09 g.chr16:3639991C>G c.3648G>C c.(3646-3648)caG>caC p.Q1216H OV 16 3647922 3647922 + Silent SNP G G A TCGA-13-0724-01A-01W-0372-09 TCGA-13-0724-10B-01W-0372-09 g.chr16:3647922G>A c.1242C>T c.(1240-1242)gaC>gaT p.D414D OV 16 3656512 3656512 + Silent SNP G G C TCGA-36-1578-01A-01W-0615-10 TCGA-36-1578-10A-01W-0615-10 g.chr16:3656512G>C c.723C>G c.(721-723)gtC>gtG p.V241V OV 16 3656526 3656526 + Missense_Mutation SNP G G A TCGA-61-2614-01A-01W-1092-09 TCGA-61-2614-10A-01W-1092-09 g.chr16:3656526G>A c.709C>T c.(709-711)Cgg>Tgg p.R237W OV 16 3658570 3658570 + Silent SNP T T C TCGA-61-1915-01A-01W-0639-09 TCGA-61-1915-11A-01W-0640-09 g.chr16:3658570T>C c.396A>G c.(394-396)gaA>gaG p.E132E PAAD 16 3639154 3639154 + Silent SNP C C T TCGA-HZ-A8P0-01A-11D-A36O-08 TCGA-HZ-A8P0-10A-01D-A367-08 g.chr16:3639154C>T c.4485G>A c.(4483-4485)gcG>gcA p.A1495A PAAD 16 3639877 3639877 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr16:3639877C>T c.3762G>A c.(3760-3762)tcG>tcA p.S1254S PAAD 16 3640331 3640331 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr16:3640331C>T c.3308G>A c.(3307-3309)cGt>cAt p.R1103H PAAD 16 3640459 3640459 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr16:3640459C>T c.3180G>A c.(3178-3180)cgG>cgA p.R1060R PAAD 16 3641221 3641221 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr16:3641221C>A c.2418G>T c.(2416-2418)gaG>gaT p.E806D PAAD 16 3652237 3652237 + Missense_Mutation SNP G G A TCGA-IB-AAUU-01A-11D-A377-08 TCGA-IB-AAUU-10A-01D-A37A-08 g.chr16:3652237G>A c.832C>T c.(832-834)Cgg>Tgg p.R278W PAAD 16 3658692 3658692 + Missense_Mutation SNP T T C TCGA-Q3-A5QY-01A-12D-A32N-08 TCGA-Q3-A5QY-10A-01D-A32N-08 g.chr16:3658692T>C c.274A>G c.(274-276)Agg>Ggg p.R92G PAAD 16 3658718 3658718 + Missense_Mutation SNP C C T TCGA-3E-AAAZ-01A-11D-A38G-08 TCGA-3E-AAAZ-10A-01D-A38J-08 g.chr16:3658718C>T c.248G>A c.(247-249)gGc>gAc p.G83D PRAD 16 3639059 3639059 + Missense_Mutation SNP G G A TCGA-KK-A7B1-01A-11D-A32B-08 TCGA-KK-A7B1-11A-12D-A329-08 g.chr16:3639059G>A c.4580C>T c.(4579-4581)cCg>cTg p.P1527L PRAD 16 3639505 3639505 + Silent SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr16:3639505C>T c.4134G>A c.(4132-4134)ccG>ccA p.P1378P PRAD 16 3640329 3640329 + Missense_Mutation SNP G G A TCGA-G9-6362-01A-11D-1786-08 TCGA-G9-6362-10A-01D-1786-08 g.chr16:3640329G>A c.3310C>T c.(3310-3312)Cgg>Tgg p.R1104W PRAD 16 3640681 3640681 + Silent SNP G G A TCGA-CH-5737-01A-11D-1576-08 TCGA-CH-5737-10A-01D-1576-08 g.chr16:3640681G>A c.2958C>T c.(2956-2958)ctC>ctT p.L986L PRAD 16 3647657 3647657 + Frame_Shift_Del DEL G G - TCGA-EJ-8469-01A-11D-2395-08 TCGA-EJ-8469-10A-01D-2395-08 g.chr16:3647657delG c.1406delC c.(1405-1407)ccafs p.P469fs PRAD 16 3656526 3656526 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr16:3656526G>A c.709C>T c.(709-711)Cgg>Tgg p.R237W PRAD 16 3658496 3658496 + Missense_Mutation SNP G G A TCGA-G9-6365-01A-11D-1786-08 TCGA-G9-6365-10A-01D-1786-08 g.chr16:3658496G>A c.470C>T c.(469-471)gCa>gTa p.A157V PRAD 16 3658512 3658512 + Missense_Mutation SNP C C G TCGA-J4-A83J-01A-11D-A364-08 TCGA-J4-A83J-10B-01D-A362-08 g.chr16:3658512C>G c.454G>C c.(454-456)Gtg>Ctg p.V152L READ 16 3632513 3632513 + Missense_Mutation SNP G G A TCGA-DC-6160-01A-11D-1657-10 TCGA-DC-6160-10A-01D-1657-10 g.chr16:3632513G>A c.5335C>T c.(5335-5337)Cgg>Tgg p.R1779W READ 16 3640008 3640008 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr16:3640008C>T c.3631G>A c.(3631-3633)Gaa>Aaa p.E1211K READ 16 3640612 3640612 + Silent SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr16:3640612G>A c.3027C>T c.(3025-3027)ggC>ggT p.G1009G READ 16 3641293 3641293 + Silent SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr16:3641293G>A c.2346C>T c.(2344-2346)ctC>ctT p.L782L READ 16 3647924 3647924 + Missense_Mutation SNP C C T TCGA-AG-3732-01A-11D-1657-10 TCGA-AG-3732-11A-01D-1657-10 g.chr16:3647924C>T c.1240G>A c.(1240-1242)Gac>Aac p.D414N READ 16 3652140 3652140 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr16:3652140C>T c.929G>A c.(928-930)cGa>cAa p.R310Q SARC 16 3641103 3641103 + Missense_Mutation SNP C C T TCGA-DX-A3UC-01A-11D-A307-09 TCGA-DX-A3UC-10A-01D-A307-09 g.chr16:3641103C>T c.2536G>A c.(2536-2538)Gtg>Atg p.V846M SARC 16 3641302 3641302 + Silent SNP C C A TCGA-QC-A7B5-01A-11D-A33E-09 TCGA-QC-A7B5-11A-11D-A33H-09 g.chr16:3641302C>A c.2337G>T c.(2335-2337)gtG>gtT p.V779V SARC 16 3646204 3646204 + Missense_Mutation SNP G G A TCGA-DX-A8BM-01A-11D-A417-09 TCGA-DX-A8BM-10B-01D-A41A-09 g.chr16:3646204G>A c.1874C>T c.(1873-1875)gCc>gTc p.A625V SKCM 16 3632512 3632512 + Missense_Mutation SNP C C T TCGA-ER-A1A1-06A-11D-A197-08 TCGA-ER-A1A1-10A-01D-A199-08 g.chr16:3632512C>T c.5336G>A c.(5335-5337)cGg>cAg p.R1779Q SKCM 16 3632567 3632567 + Missense_Mutation SNP G G A TCGA-EE-A3AB-06A-11D-A196-08 TCGA-EE-A3AB-10A-01D-A198-08 g.chr16:3632567G>A c.5281C>T c.(5281-5283)Cgc>Tgc p.R1761C SKCM 16 3632685 3632685 + Silent SNP G G A TCGA-D3-A2JA-06A-11D-A196-08 TCGA-D3-A2JA-10A-01D-A198-08 g.chr16:3632685G>A c.5163C>T c.(5161-5163)tcC>tcT p.S1721S SKCM 16 3632689 3632689 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr16:3632689G>A c.5159C>T c.(5158-5160)tCc>tTc p.S1720F SKCM 16 3633161 3633161 + Missense_Mutation SNP G G A TCGA-EE-A2GR-06A-11D-A197-08 TCGA-EE-A2GR-10A-01D-A199-08 g.chr16:3633161G>A c.5090C>T c.(5089-5091)cCa>cTa p.P1697L SKCM 16 3633209 3633209 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr16:3633209G>A c.5042C>T c.(5041-5043)tCg>tTg p.S1681L SKCM 16 3633257 3633257 + Missense_Mutation SNP G G A TCGA-EE-A2MD-06A-11D-A197-08 TCGA-EE-A2MD-10A-01D-A199-08 g.chr16:3633257G>A c.4994C>T c.(4993-4995)cCc>cTc p.P1665L SKCM 16 3633395 3633395 + Missense_Mutation SNP G G A TCGA-EE-A3AA-06A-11D-A196-08 TCGA-EE-A3AA-10A-01D-A198-08 g.chr16:3633395G>A c.4856C>T c.(4855-4857)cCg>cTg p.P1619L SKCM 16 3633422 3633422 + Missense_Mutation SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr16:3633422G>A c.4829C>T c.(4828-4830)tCc>tTc p.S1610F SKCM 16 3633495 3633495 + Silent SNP G G A TCGA-D3-A2JH-06A-11D-A196-08 TCGA-D3-A2JH-10A-01D-A198-08 g.chr16:3633495G>A c.4756C>T c.(4756-4758)Ctg>Ttg p.L1586L SKCM 16 3639232 3639232 + Silent SNP G G A TCGA-EB-A5UN-06A-11D-A30X-08 TCGA-EB-A5UN-10A-01D-A30X-08 g.chr16:3639232G>A c.4407C>T c.(4405-4407)tcC>tcT p.S1469S SKCM 16 3639257 3639257 + Missense_Mutation SNP G G A TCGA-D3-A3MR-06A-11D-A21A-08 TCGA-D3-A3MR-10A-01D-A21A-08 g.chr16:3639257G>A c.4382C>T c.(4381-4383)gCc>gTc p.A1461V SKCM 16 3639374 3639374 + Missense_Mutation SNP G G A TCGA-D3-A51J-06A-11D-A25O-08 TCGA-D3-A51J-10A-01D-A25O-08 g.chr16:3639374G>A c.4265C>T c.(4264-4266)cCa>cTa p.P1422L SKCM 16 3639402 3639402 + Missense_Mutation SNP G G A TCGA-FS-A1ZZ-06A-11D-A197-08 TCGA-FS-A1ZZ-10A-01D-A199-08 g.chr16:3639402G>A c.4237C>T c.(4237-4239)Ccc>Tcc p.P1413S SKCM 16 3639432 3639432 + Missense_Mutation SNP C C T TCGA-DA-A1IC-06A-11D-A197-08 TCGA-DA-A1IC-10A-01D-A199-08 g.chr16:3639432C>T c.4207G>A c.(4207-4209)Gag>Aag p.E1403K SKCM 16 3639611 3639611 + Missense_Mutation SNP G G A TCGA-FS-A1ZW-06A-12D-A197-08 TCGA-FS-A1ZW-10A-01D-A199-08 g.chr16:3639611G>A c.4028C>T c.(4027-4029)cCt>cTt p.P1343L SKCM 16 3639678 3639678 + Missense_Mutation SNP G G A TCGA-EE-A2GC-06A-11D-A197-08 TCGA-EE-A2GC-10A-01D-A199-08 g.chr16:3639678G>A c.3961C>T c.(3961-3963)Ccg>Tcg p.P1321S SKCM 16 3639790 3639790 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr16:3639790G>A c.3849C>T c.(3847-3849)gcC>gcT p.A1283A SKCM 16 3639858 3639858 + Missense_Mutation SNP G G A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr16:3639858G>A c.3781C>T c.(3781-3783)Ccg>Tcg p.P1261S SKCM 16 3640116 3640116 + Missense_Mutation SNP G G A TCGA-FS-A1ZZ-06A-11D-A197-08 TCGA-FS-A1ZZ-10A-01D-A199-08 g.chr16:3640116G>A c.3523C>T c.(3523-3525)Cct>Tct p.P1175S SKCM 16 3640281 3640281 + Missense_Mutation SNP T T G TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr16:3640281T>G c.3358A>C c.(3358-3360)Aaa>Caa p.K1120Q SKCM 16 3640456 3640456 + Silent SNP G G A TCGA-D3-A51T-06A-11D-A25O-08 TCGA-D3-A51T-10A-01D-A25O-08 g.chr16:3640456G>A c.3183C>T c.(3181-3183)tcC>tcT p.S1061S SKCM 16 3640461 3640461 + Missense_Mutation SNP G G A TCGA-EE-A2GI-06A-11D-A196-08 TCGA-EE-A2GI-10A-01D-A198-08 g.chr16:3640461G>A c.3178C>T c.(3178-3180)Cgg>Tgg p.R1060W SKCM 16 3640462 3640462 + Silent SNP G G A TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr16:3640462G>A c.3177C>T c.(3175-3177)ccC>ccT p.P1059P SKCM 16 3640463 3640463 + Missense_Mutation SNP G G A TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr16:3640463G>A c.3176C>T c.(3175-3177)cCc>cTc p.P1059L SKCM 16 3640520 3640520 + Missense_Mutation SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr16:3640520G>A c.3119C>T c.(3118-3120)cCc>cTc p.P1040L SKCM 16 3640521 3640521 + Missense_Mutation SNP G G A TCGA-EE-A2A2-06A-11D-A196-08 TCGA-EE-A2A2-10A-01D-A198-08 g.chr16:3640521G>A c.3118C>T c.(3118-3120)Ccc>Tcc p.P1040S SKCM 16 3640889 3640889 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr16:3640889G>A c.2750C>T c.(2749-2751)gCc>gTc p.A917V SKCM 16 3640985 3640985 + Missense_Mutation SNP G G T TCGA-EE-A2MQ-06A-11D-A197-08 TCGA-EE-A2MQ-10A-01D-A199-08 g.chr16:3640985G>T c.2654C>A c.(2653-2655)cCg>cAg p.P885Q SKCM 16 3641088 3641088 + Missense_Mutation SNP T T C TCGA-EE-A29V-06A-12D-A197-08 TCGA-EE-A29V-10A-01D-A199-08 g.chr16:3641088T>C c.2551A>G c.(2551-2553)Atg>Gtg p.M851V SKCM 16 3641185 3641185 + Silent SNP G G A TCGA-EE-A29Q-06A-11D-A197-08 TCGA-EE-A29Q-10A-01D-A199-08 g.chr16:3641185G>A c.2454C>T c.(2452-2454)ctC>ctT p.L818L SKCM 16 3644580 3644580 + Silent SNP A A C TCGA-DA-A1I4-06A-11D-A196-08 TCGA-DA-A1I4-10A-01D-A198-08 g.chr16:3644580A>C c.2034T>G c.(2032-2034)gtT>gtG p.V678V SKCM 16 3645678 3645678 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr16:3645678G>A c.1941C>T c.(1939-1941)ccC>ccT p.P647P SKCM 16 3652243 3652243 + Missense_Mutation SNP A A G TCGA-FS-A1ZZ-06A-11D-A197-08 TCGA-FS-A1ZZ-10A-01D-A199-08 g.chr16:3652243A>G c.826T>C c.(826-828)Ttt>Ctt p.F276L SKCM 16 3656630 3656630 + Missense_Mutation SNP T T G TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr16:3656630T>G c.605A>C c.(604-606)aAa>aCa p.K202T SKCM 16 3658452 3658452 + Missense_Mutation SNP G G A TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr16:3658452G>A c.514C>T c.(514-516)Ctt>Ttt p.L172F SKCM 16 3658900 3658900 + Silent SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr16:3658900G>A c.66C>T c.(64-66)gcC>gcT p.A22A

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 16 3640405 3640405 single base substitution C G synonymous_variant V1078V 3234G>C BLCA-CN 16 3651099 3651099 single base substitution G T exon_variant BLCA-CN 16 3651099 3651099 single base substitution G T missense_variant S348R 1044C>A BLCA-US 16 3633236 3633236 single base substitution T C missense_variant H1672R 5015A>G BLCA-US 16 3639978 3639978 single base substitution C A missense_variant A1221S 3661G>T BLCA-US 16 3640211 3640211 single base substitution G A missense_variant S1143F 3428C>T BLCA-US 16 3640791 3640791 single base substitution C G downstream_gene_variant BLCA-US 16 3640791 3640791 single base substitution C G missense_variant E950Q 2848G>C BLCA-US 16 3641148 3641148 single base substitution C A downstream_gene_variant BLCA-US 16 3641148 3641148 single base substitution C A stop_gained E831* 2491G>T BLCA-US 16 3641190 3641190 single base substitution C T downstream_gene_variant BLCA-US 16 3641190 3641190 single base substitution C T missense_variant E817K 2449G>A BLCA-US 16 3656547 3656547 single base substitution C T exon_variant BLCA-US 16 3656547 3656547 single base substitution C T missense_variant E230K 688G>A BOCA-FR 16 3661139 3661139 single base substitution C T intron_variant BOCA-FR 16 3661139 3661139 single base substitution C T upstream_gene_variant BRCA-EU 16 3626202 3626202 single base substitution G A downstream_gene_variant BRCA-EU 16 3626446 3626446 single base substitution G C downstream_gene_variant BRCA-EU 16 3626467 3626467 single base substitution G A downstream_gene_variant BRCA-EU 16 3627444 3627444 single base substitution T A downstream_gene_variant BRCA-EU 16 3629097 3629097 single base substitution C T downstream_gene_variant BRCA-EU 16 3629721 3629721 single base substitution C T downstream_gene_variant BRCA-EU 16 3630951 3630951 single base substitution A T downstream_gene_variant BRCA-EU 16 3634120 3634120 single base substitution C G intron_variant BRCA-EU 16 3634821 3634821 single base substitution A G missense_variant M1563T 4688T>C BRCA-EU 16 3635403 3635403 single base substitution C T intron_variant BRCA-EU 16 3637323 3637323 single base substitution C A intron_variant BRCA-EU 16 3637391 3637391 single base substitution G T intron_variant BRCA-EU 16 3637401 3637401 single base substitution G T intron_variant BRCA-EU 16 3638490 3638490 single base substitution C T intron_variant BRCA-EU 16 3638537 3638537 single base substitution C G intron_variant BRCA-EU 16 3640008 3640008 single base substitution C T missense_variant E1211K 3631G>A BRCA-EU 16 3640055 3640055 single base substitution A G missense_variant I1195T 3584T>C BRCA-EU 16 3642139 3642139 single base substitution G A downstream_gene_variant BRCA-EU 16 3642139 3642139 single base substitution G A intron_variant BRCA-EU 16 3643548 3643548 single base substitution G A downstream_gene_variant BRCA-EU 16 3643548 3643548 single base substitution G A intron_variant BRCA-EU 16 3643562 3643562 single base substitution C A downstream_gene_variant BRCA-EU 16 3643562 3643562 single base substitution C A intron_variant BRCA-EU 16 3643838 3643838 single base substitution G C downstream_gene_variant BRCA-EU 16 3643838 3643838 single base substitution G C intron_variant BRCA-EU 16 3644225 3644225 single base substitution C T downstream_gene_variant BRCA-EU 16 3644225 3644225 single base substitution C T intron_variant BRCA-EU 16 3644957 3644957 single base substitution C A downstream_gene_variant BRCA-EU 16 3644957 3644957 single base substitution C A intron_variant BRCA-EU 16 3645223 3645223 single base substitution G A downstream_gene_variant BRCA-EU 16 3645223 3645223 single base substitution G A intron_variant BRCA-EU 16 3646096 3646096 single base substitution C T downstream_gene_variant BRCA-EU 16 3646096 3646096 single base substitution C T intron_variant BRCA-EU 16 3646270 3646270 single base substitution G A downstream_gene_variant BRCA-EU 16 3646270 3646270 single base substitution G A exon_variant BRCA-EU 16 3646270 3646270 single base substitution G A missense_variant S603L 1808C>T BRCA-EU 16 3648283 3648283 single base substitution C T downstream_gene_variant BRCA-EU 16 3648283 3648283 single base substitution C T intron_variant BRCA-EU 16 3649393 3649393 single base substitution C T downstream_gene_variant BRCA-EU 16 3649393 3649393 single base substitution C T intron_variant BRCA-EU 16 3649589 3649589 single base substitution T A downstream_gene_variant BRCA-EU 16 3649589 3649589 single base substitution T A intron_variant BRCA-EU 16 3651118 3651118 single base substitution G A exon_variant BRCA-EU 16 3651118 3651118 single base substitution G A missense_variant P342L 1025C>T BRCA-EU 16 3652558 3652558 single base substitution G C intron_variant BRCA-EU 16 3652723 3652723 single base substitution C T intron_variant BRCA-EU 16 3653090 3653090 single base substitution C G intron_variant BRCA-EU 16 3653761 3653761 single base substitution T C intron_variant BRCA-EU 16 3655276 3655276 single base substitution G A intron_variant BRCA-EU 16 3655548 3655548 single base substitution C A intron_variant BRCA-EU 16 3657195 3657195 single base substitution G A intron_variant BRCA-EU 16 3659732 3659732 single base substitution A C intron_variant BRCA-EU 16 3659732 3659732 single base substitution A C upstream_gene_variant BRCA-EU 16 3659934 3659934 single base substitution G T intron_variant BRCA-EU 16 3659934 3659934 single base substitution G T upstream_gene_variant BRCA-EU 16 3660702 3660702 single base substitution C T intron_variant BRCA-EU 16 3660702 3660702 single base substitution C T upstream_gene_variant BRCA-EU 16 3661614 3661614 single base substitution G C upstream_gene_variant BRCA-EU 16 3662249 3662249 insertion of <=200bp - T upstream_gene_variant BRCA-EU 16 3662448 3662448 single base substitution C A upstream_gene_variant BRCA-EU 16 3664216 3664216 insertion of <=200bp - T upstream_gene_variant BRCA-EU 16 3666545 3666545 single base substitution C A upstream_gene_variant BRCA-FR 16 3626467 3626467 single base substitution G A downstream_gene_variant BRCA-FR 16 3633394 3633394 single base substitution C T synonymous_variant P1619P 4857G>A BRCA-FR 16 3633871 3633871 single base substitution G A intron_variant BRCA-FR 16 3643838 3643838 single base substitution G C downstream_gene_variant BRCA-FR 16 3643838 3643838 single base substitution G C intron_variant BRCA-FR 16 3648283 3648283 single base substitution C T downstream_gene_variant BRCA-FR 16 3648283 3648283 single base substitution C T intron_variant BRCA-FR 16 3649393 3649393 single base substitution C T downstream_gene_variant BRCA-FR 16 3649393 3649393 single base substitution C T intron_variant BRCA-FR 16 3655276 3655276 single base substitution G A intron_variant BRCA-FR 16 3655548 3655548 single base substitution C A intron_variant BRCA-FR 16 3659934 3659934 single base substitution G T intron_variant BRCA-FR 16 3659934 3659934 single base substitution G T upstream_gene_variant BRCA-FR 16 3661805 3661805 single base substitution G C upstream_gene_variant BRCA-FR 16 3662448 3662448 single base substitution C A upstream_gene_variant BRCA-UK 16 3630350 3630350 single base substitution C G downstream_gene_variant BRCA-UK 16 3635403 3635403 single base substitution C T intron_variant BRCA-UK 16 3638579 3638579 single base substitution G C intron_variant BRCA-UK 16 3647695 3647695 single base substitution C G downstream_gene_variant BRCA-UK 16 3647695 3647695 single base substitution C G missense_variant E456D 1368G>C BRCA-UK 16 3647695 3647695 single base substitution C G splice_region_variant BRCA-UK 16 3660729 3660729 single base substitution C A intron_variant BRCA-UK 16 3660729 3660729 single base substitution C A upstream_gene_variant BRCA-US 16 3632422 3632422 single base substitution G C missense_variant T1809S 5426C>G BRCA-US 16 3632522 3632522 insertion of <=200bp - G frameshift_variant F1776S? BRCA-US 16 3633370 3633370 single base substitution C G missense_variant Q1627H 4881G>C BRCA-US 16 3639839 3639839 single base substitution C T missense_variant R1267H 3800G>A BRCA-US 16 3640194 3640194 single base substitution C A missense_variant D1149Y 3445G>T BRCA-US 16 3641097 3641097 single base substitution C T downstream_gene_variant BRCA-US 16 3641097 3641097 single base substitution C T missense_variant E848K 2542G>A BRCA-US 16 3656563 3656563 single base substitution C A exon_variant BRCA-US 16 3656563 3656563 single base substitution C A missense_variant L224F 672G>T BRCA-US 16 3658860 3658860 single base substitution C T exon_variant BRCA-US 16 3658860 3658860 single base substitution C T missense_variant E36K 106G>A BTCA-JP 16 3627086 3627086 single base substitution C A downstream_gene_variant BTCA-JP 16 3639335 3639335 single base substitution G T missense_variant P1435Q 4304C>A BTCA-JP 16 3639766 3639766 single base substitution C T synonymous_variant T1291T 3873G>A BTCA-JP 16 3640699 3640699 single base substitution G A downstream_gene_variant BTCA-JP 16 3640699 3640699 single base substitution G A synonymous_variant A980A 2940C>T BTCA-JP 16 3640860 3640860 single base substitution C T downstream_gene_variant BTCA-JP 16 3640860 3640860 single base substitution C T missense_variant A927T 2779G>A BTCA-JP 16 3652321 3652321 single base substitution A G intron_variant BTCA-JP 16 3658776 3658776 single base substitution T G exon_variant BTCA-JP 16 3658776 3658776 single base substitution T G missense_variant K64Q 190A>C BTCA-JP 16 3658794 3658794 single base substitution A C exon_variant BTCA-JP 16 3658794 3658794 single base substitution A C missense_variant F58V 172T>G CESC-US 16 3632683 3632683 single base substitution C G missense_variant C1722S 5165G>C CESC-US 16 3639021 3639021 single base substitution C T missense_variant E1540K 4618G>A CESC-US 16 3656621 3656621 single base substitution G A exon_variant CESC-US 16 3656621 3656621 single base substitution G A missense_variant T205I 614C>T COAD-US 16 3632466 3632466 single base substitution C T synonymous_variant S1794S 5382G>A COAD-US 16 3632640 3632640 single base substitution G A synonymous_variant G1736G 5208C>T COAD-US 16 3639043 3639043 single base substitution G A synonymous_variant S1532S 4596C>T COAD-US 16 3639398 3639398 deletion of <=200bp G - frameshift_variant P1414 COAD-US 16 3639737 3639737 single base substitution C T missense_variant G1301E 3902G>A COAD-US 16 3639918 3639918 single base substitution G A missense_variant R1241C 3721C>T COAD-US 16 3639963 3639963 single base substitution G A missense_variant R1226W 3676C>T COAD-US 16 3639972 3639972 single base substitution G A missense_variant P1223S 3667C>T COAD-US 16 3639977 3639977 single base substitution G A missense_variant A1221V 3662C>T COAD-US 16 3640733 3640733 single base substitution C A downstream_gene_variant COAD-US 16 3640733 3640733 single base substitution C A missense_variant R969I 2906G>T COAD-US 16 3640784 3640784 single base substitution G A downstream_gene_variant COAD-US 16 3640784 3640784 single base substitution G A missense_variant A952V 2855C>T COAD-US 16 3640785 3640785 single base substitution C T downstream_gene_variant COAD-US 16 3640785 3640785 single base substitution C T missense_variant A952T 2854G>A COAD-US 16 3641200 3641200 single base substitution C A downstream_gene_variant COAD-US 16 3641200 3641200 single base substitution C A missense_variant E813D 2439G>T COAD-US 16 3646191 3646191 single base substitution G A downstream_gene_variant COAD-US 16 3646191 3646191 single base substitution G A exon_variant COAD-US 16 3646191 3646191 single base substitution G A synonymous_variant P629P 1887C>T COAD-US 16 3646333 3646333 single base substitution C T downstream_gene_variant COAD-US 16 3646333 3646333 single base substitution C T exon_variant COAD-US 16 3646333 3646333 single base substitution C T missense_variant R582Q 1745G>A COAD-US 16 3647390 3647390 single base substitution C T downstream_gene_variant COAD-US 16 3647390 3647390 single base substitution C T exon_variant COAD-US 16 3647390 3647390 single base substitution C T missense_variant R558Q 1673G>A COAD-US 16 3647433 3647433 single base substitution C A downstream_gene_variant COAD-US 16 3647433 3647433 single base substitution C A exon_variant COAD-US 16 3647433 3647433 single base substitution C A missense_variant D544Y 1630G>T COAD-US 16 3647914 3647914 single base substitution G T downstream_gene_variant COAD-US 16 3647914 3647914 single base substitution G T exon_variant COAD-US 16 3647914 3647914 single base substitution G T missense_variant P417Q 1250C>A COAD-US 16 3652148 3652148 single base substitution G A exon_variant COAD-US 16 3652148 3652148 single base substitution G A synonymous_variant N307N 921C>T COAD-US 16 3656526 3656526 single base substitution G A exon_variant COAD-US 16 3656526 3656526 single base substitution G A missense_variant R237W 709C>T COCA-CN 16 3633047 3633047 single base substitution C T intron_variant COCA-CN 16 3633284 3633284 single base substitution G T missense_variant P1656H 4967C>A COCA-CN 16 3633581 3633581 single base substitution A G intron_variant COCA-CN 16 3639413 3639413 single base substitution G A missense_variant A1409V 4226C>T COCA-CN 16 3640455 3640455 single base substitution G A missense_variant R1062C 3184C>T COCA-CN 16 3640571 3640571 single base substitution G T missense_variant A1023D 3068C>A COCA-CN 16 3640580 3640580 single base substitution T C missense_variant H1020R 3059A>G COCA-CN 16 3640615 3640615 single base substitution A C downstream_gene_variant COCA-CN 16 3640615 3640615 single base substitution A C missense_variant S1008R 3024T>G COCA-CN 16 3641218 3641218 single base substitution A G downstream_gene_variant COCA-CN 16 3641218 3641218 single base substitution A G synonymous_variant N807N 2421T>C COCA-CN 16 3647763 3647763 single base substitution G A downstream_gene_variant COCA-CN 16 3647763 3647763 single base substitution G A intron_variant COCA-CN 16 3652088 3652088 single base substitution C T exon_variant COCA-CN 16 3652088 3652088 single base substitution C T intron_variant COCA-CN 16 3656600 3656600 single base substitution C T exon_variant COCA-CN 16 3656600 3656600 single base substitution C T missense_variant R212Q 635G>A EOPC-DE 16 3649566 3649566 single base substitution C T downstream_gene_variant EOPC-DE 16 3649566 3649566 single base substitution C T intron_variant EOPC-DE 16 3659671 3659671 single base substitution A C intron_variant EOPC-DE 16 3659671 3659671 single base substitution A C upstream_gene_variant ESAD-UK 16 3627519 3627519 single base substitution C T downstream_gene_variant ESAD-UK 16 3628223 3628223 single base substitution G T downstream_gene_variant ESAD-UK 16 3629302 3629302 single base substitution C T downstream_gene_variant ESAD-UK 16 3631030 3631030 single base substitution C A downstream_gene_variant ESAD-UK 16 3632424 3632424 single base substitution G A synonymous_variant F1808F 5424C>T ESAD-UK 16 3632824 3632824 single base substitution G C intron_variant ESAD-UK 16 3633755 3633755 single base substitution G A intron_variant ESAD-UK 16 3633835 3633835 single base substitution C T intron_variant ESAD-UK 16 3633925 3633925 single base substitution G A intron_variant ESAD-UK 16 3638028 3638028 single base substitution C A intron_variant ESAD-UK 16 3638809 3638809 single base substitution G A intron_variant ESAD-UK 16 3638898 3638898 single base substitution G A intron_variant ESAD-UK 16 3639159 3639159 single base substitution C T missense_variant G1494S 4480G>A ESAD-UK 16 3646033 3646033 single base substitution C T downstream_gene_variant ESAD-UK 16 3646033 3646033 single base substitution C T intron_variant ESAD-UK 16 3646586 3646586 single base substitution T G downstream_gene_variant ESAD-UK 16 3646586 3646586 single base substitution T G intron_variant ESAD-UK 16 3650324 3650324 single base substitution C G downstream_gene_variant ESAD-UK 16 3650324 3650324 single base substitution C G intron_variant ESAD-UK 16 3650808 3650808 single base substitution G A exon_variant ESAD-UK 16 3650808 3650808 single base substitution G A intron_variant ESAD-UK 16 3659739 3659739 single base substitution A G intron_variant ESAD-UK 16 3659739 3659739 single base substitution A G upstream_gene_variant ESAD-UK 16 3666293 3666293 insertion of <=200bp - T upstream_gene_variant GBM-US 16 3642834 3642834 single base substitution G A downstream_gene_variant GBM-US 16 3642834 3642834 single base substitution G A synonymous_variant D731D 2193C>T GBM-US 16 3658781 3658781 single base substitution A G exon_variant GBM-US 16 3658781 3658781 single base substitution A G missense_variant V62A 185T>C KIRC-US 16 3639200 3639200 single base substitution C T missense_variant G1480E 4439G>A KIRC-US 16 3640657 3640657 single base substitution G T downstream_gene_variant KIRC-US 16 3640657 3640657 single base substitution G T synonymous_variant I994I 2982C>A KIRC-US 16 3641170 3641170 single base substitution C T downstream_gene_variant KIRC-US 16 3641170 3641170 single base substitution C T stop_gained W823* 2469G>A KIRC-US 16 3641179 3641179 single base substitution C A downstream_gene_variant KIRC-US 16 3641179 3641179 single base substitution C A missense_variant R820S 2460G>T KIRC-US 16 3652234 3652234 single base substitution C T exon_variant KIRC-US 16 3652234 3652234 single base substitution C T missense_variant V279I 835G>A KIRC-US 16 3658538 3658538 single base substitution A T exon_variant KIRC-US 16 3658538 3658538 single base substitution A T missense_variant V143E 428T>A KIRP-US 16 3645657 3645657 deletion of <=200bp C - downstream_gene_variant KIRP-US 16 3645657 3645657 deletion of <=200bp C - exon_variant KIRP-US 16 3645657 3645657 deletion of <=200bp C - frameshift_variant G654 LAML-KR 16 3635579 3635579 single base substitution T C intron_variant LAML-KR 16 3663933 3663933 single base substitution G T upstream_gene_variant LGG-US 16 3640627 3640627 single base substitution G A downstream_gene_variant LGG-US 16 3640627 3640627 single base substitution G A synonymous_variant P1004P 3012C>T LGG-US 16 3640690 3640690 single base substitution G A downstream_gene_variant LGG-US 16 3640690 3640690 single base substitution G A synonymous_variant Y983Y 2949C>T LICA-CN 16 3647489 3647489 single base substitution C A downstream_gene_variant LICA-CN 16 3647489 3647489 single base substitution C A exon_variant LICA-CN 16 3647489 3647489 single base substitution C A missense_variant R525L 1574G>T LICA-CN 16 3647872 3647872 single base substitution T A downstream_gene_variant LICA-CN 16 3647872 3647872 single base substitution T A exon_variant LICA-CN 16 3647872 3647872 single base substitution T A missense_variant E431V 1292A>T LICA-CN 16 3658510 3658510 single base substitution C A exon_variant LICA-CN 16 3658510 3658510 single base substitution C A synonymous_variant V152V 456G>T LICA-CN 16 3658640 3658640 single base substitution T C exon_variant LICA-CN 16 3658640 3658640 single base substitution T C missense_variant K109R 326A>G LICA-FR 16 3634806 3634806 single base substitution A G missense_variant I1568T 4703T>C LICA-FR 16 3640010 3640010 single base substitution C T missense_variant S1210N 3629G>A LICA-FR 16 3640582 3640582 single base substitution A G synonymous_variant S1019S 3057T>C LICA-FR 16 3644467 3644467 single base substitution A C downstream_gene_variant LICA-FR 16 3644467 3644467 single base substitution A C missense_variant L716R 2147T>G LICA-FR 16 3646315 3646315 single base substitution T C downstream_gene_variant LICA-FR 16 3646315 3646315 single base substitution T C exon_variant LICA-FR 16 3646315 3646315 single base substitution T C missense_variant H588R 1763A>G LICA-FR 16 3650987 3650987 single base substitution T C exon_variant LICA-FR 16 3650987 3650987 single base substitution T C missense_variant M386V 1156A>G LICA-FR 16 3656600 3656600 single base substitution C T exon_variant LICA-FR 16 3656600 3656600 single base substitution C T missense_variant R212Q 635G>A LIHC-US 16 3634828 3634828 single base substitution T C missense_variant T1561A 4681A>G LIHC-US 16 3642739 3642739 single base substitution G T downstream_gene_variant LIHC-US 16 3642739 3642739 single base substitution G T missense_variant P763H 2288C>A LIHC-US 16 3651153 3651153 single base substitution C A exon_variant LIHC-US 16 3651153 3651153 single base substitution C A synonymous_variant V330V 990G>T LINC-JP 16 3626367 3626367 single base substitution G A downstream_gene_variant LINC-JP 16 3638948 3638948 single base substitution T C intron_variant LINC-JP 16 3638998 3638998 single base substitution C T splice_region_variant LINC-JP 16 3639055 3639055 single base substitution G T synonymous_variant A1528A 4584C>A LINC-JP 16 3640796 3640796 single base substitution G A downstream_gene_variant LINC-JP 16 3640796 3640796 single base substitution G A missense_variant A948V 2843C>T LINC-JP 16 3646035 3646035 single base substitution C A downstream_gene_variant LINC-JP 16 3646035 3646035 single base substitution C A intron_variant LINC-JP 16 3657654 3657654 single base substitution C A intron_variant LINC-JP 16 3658346 3658346 single base substitution T A intron_variant LIRI-JP 16 3626937 3626937 single base substitution T C downstream_gene_variant LIRI-JP 16 3630020 3630020 single base substitution C A downstream_gene_variant LIRI-JP 16 3632947 3632947 single base substitution C T intron_variant LIRI-JP 16 3639058 3639058 single base substitution C T synonymous_variant P1527P 4581G>A LIRI-JP 16 3639238 3639238 single base substitution A G synonymous_variant C1467C 4401T>C LIRI-JP 16 3648401 3648401 single base substitution C G downstream_gene_variant LIRI-JP 16 3648401 3648401 single base substitution C G intron_variant LIRI-JP 16 3650220 3650220 single base substitution C A downstream_gene_variant LIRI-JP 16 3650220 3650220 single base substitution C A intron_variant LIRI-JP 16 3652274 3652274 single base substitution G A exon_variant LIRI-JP 16 3652274 3652274 single base substitution G A synonymous_variant D265D 795C>T LIRI-JP 16 3652526 3652526 single base substitution T C intron_variant LIRI-JP 16 3656301 3656301 deletion of <=200bp A - intron_variant LIRI-JP 16 3657477 3657477 single base substitution A T intron_variant LIRI-JP 16 3658074 3658074 single base substitution A G intron_variant LIRI-JP 16 3658132 3658132 single base substitution G A intron_variant LIRI-JP 16 3658549 3658549 single base substitution C T exon_variant LIRI-JP 16 3658549 3658549 single base substitution C T synonymous_variant G139G 417G>A LIRI-JP 16 3660208 3660208 single base substitution T C intron_variant LIRI-JP 16 3660208 3660208 single base substitution T C upstream_gene_variant LIRI-JP 16 3660840 3660844 deletion of <=200bp AGAAA - intron_variant LIRI-JP 16 3660840 3660844 deletion of <=200bp AGAAA - upstream_gene_variant LUSC-KR 16 3627339 3627339 single base substitution G A downstream_gene_variant LUSC-KR 16 3627344 3627344 single base substitution G T downstream_gene_variant LUSC-KR 16 3627358 3627358 single base substitution C T downstream_gene_variant LUSC-KR 16 3630486 3630486 single base substitution G A downstream_gene_variant LUSC-KR 16 3630497 3630497 single base substitution C T downstream_gene_variant LUSC-KR 16 3636163 3636163 single base substitution G T intron_variant LUSC-KR 16 3639139 3639139 single base substitution A G synonymous_variant N1500N 4500T>C LUSC-KR 16 3639227 3639227 single base substitution C T missense_variant G1471E 4412G>A LUSC-KR 16 3639861 3639861 single base substitution T G missense_variant T1260P 3778A>C LUSC-KR 16 3642781 3642781 single base substitution C A downstream_gene_variant LUSC-KR 16 3642781 3642781 single base substitution C A missense_variant R749L 2246G>T LUSC-KR 16 3648953 3648953 single base substitution T A downstream_gene_variant LUSC-KR 16 3648953 3648953 single base substitution T A intron_variant LUSC-KR 16 3653290 3653290 single base substitution C T intron_variant LUSC-KR 16 3656482 3656482 single base substitution C T exon_variant LUSC-KR 16 3656482 3656482 single base substitution C T synonymous_variant A251A 753G>A LUSC-KR 16 3661753 3661753 single base substitution G T upstream_gene_variant LUSC-KR 16 3661754 3661754 single base substitution G T upstream_gene_variant LUSC-US 16 3633150 3633150 single base substitution C G missense_variant E1701Q 5101G>C LUSC-US 16 3633448 3633448 single base substitution G T stop_gained Y1601* 4803C>A LUSC-US 16 3639381 3639381 single base substitution G A missense_variant P1420S 4258C>T LUSC-US 16 3640826 3640826 single base substitution G T downstream_gene_variant LUSC-US 16 3640826 3640826 single base substitution G T missense_variant A938E 2813C>A LUSC-US 16 3641118 3641118 single base substitution C G downstream_gene_variant LUSC-US 16 3641118 3641118 single base substitution C G missense_variant E841Q 2521G>C LUSC-US 16 3641121 3641121 single base substitution C G downstream_gene_variant LUSC-US 16 3641121 3641121 single base substitution C G missense_variant E840Q 2518G>C LUSC-US 16 3652259 3652259 single base substitution C G exon_variant LUSC-US 16 3652259 3652259 single base substitution C G missense_variant L270F 810G>C LUSC-US 16 3656624 3656624 single base substitution C T exon_variant LUSC-US 16 3656624 3656624 single base substitution C T missense_variant R204H 611G>A LUSC-US 16 3658448 3658448 single base substitution G C exon_variant LUSC-US 16 3658448 3658448 single base substitution G C missense_variant S173C 518C>G LUSC-US 16 3658604 3658604 single base substitution T C exon_variant LUSC-US 16 3658604 3658604 single base substitution T C missense_variant K121R 362A>G LUSC-US 16 3658855 3658855 single base substitution G T exon_variant LUSC-US 16 3658855 3658855 single base substitution G T missense_variant S37R 111C>A MALY-DE 16 3629910 3629910 single base substitution G C downstream_gene_variant MALY-DE 16 3630625 3630625 single base substitution T C downstream_gene_variant MALY-DE 16 3644861 3644861 single base substitution A C downstream_gene_variant MALY-DE 16 3644861 3644861 single base substitution A C intron_variant MALY-DE 16 3646352 3646352 single base substitution G A downstream_gene_variant MALY-DE 16 3646352 3646352 single base substitution G A exon_variant MALY-DE 16 3646352 3646352 single base substitution G A missense_variant H576Y 1726C>T MALY-DE 16 3654134 3654134 single base substitution G A intron_variant MALY-DE 16 3663629 3663629 single base substitution C T upstream_gene_variant MALY-DE 16 3664618 3664618 single base substitution G A upstream_gene_variant MALY-DE 16 3665618 3665618 single base substitution G A upstream_gene_variant MELA-AU 16 3626459 3626459 single base substitution C T downstream_gene_variant MELA-AU 16 3626909 3626909 single base substitution G A downstream_gene_variant MELA-AU 16 3627109 3627109 single base substitution C T downstream_gene_variant MELA-AU 16 3628847 3628847 single base substitution C T downstream_gene_variant MELA-AU 16 3629368 3629369 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 16 3630938 3630938 single base substitution G A downstream_gene_variant MELA-AU 16 3631088 3631088 single base substitution G A downstream_gene_variant MELA-AU 16 3631938 3631938 single base substitution G A 3_prime_UTR_variant MELA-AU 16 3632069 3632069 single base substitution A C 3_prime_UTR_variant MELA-AU 16 3632099 3632099 single base substitution G A 3_prime_UTR_variant MELA-AU 16 3632246 3632247 multiple base substitution (>=2bp and <=200bp) GG AT 3_prime_UTR_variant MELA-AU 16 3632333 3632333 single base substitution G A 3_prime_UTR_variant MELA-AU 16 3632697 3632697 single base substitution G A intron_variant MELA-AU 16 3632866 3632866 single base substitution G A intron_variant MELA-AU 16 3632904 3632904 single base substitution G A intron_variant MELA-AU 16 3633085 3633085 single base substitution T C intron_variant MELA-AU 16 3633162 3633163 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant IP1696IS MELA-AU 16 3633257 3633257 single base substitution G A missense_variant P1665L 4994C>T MELA-AU 16 3633395 3633395 single base substitution G A missense_variant P1619L 4856C>T MELA-AU 16 3633518 3633518 single base substitution G A splice_region_variant MELA-AU 16 3633776 3633776 single base substitution G A intron_variant MELA-AU 16 3633813 3633813 single base substitution G T intron_variant MELA-AU 16 3634044 3634044 single base substitution G A intron_variant MELA-AU 16 3634078 3634078 single base substitution G A intron_variant MELA-AU 16 3634243 3634243 single base substitution G A intron_variant MELA-AU 16 3634690 3634690 single base substitution C T intron_variant MELA-AU 16 3634728 3634728 single base substitution G A intron_variant MELA-AU 16 3634911 3634911 single base substitution G A intron_variant MELA-AU 16 3635108 3635108 single base substitution G A intron_variant MELA-AU 16 3635495 3635495 single base substitution G A intron_variant MELA-AU 16 3635898 3635898 single base substitution G A intron_variant MELA-AU 16 3635983 3635983 single base substitution G A intron_variant MELA-AU 16 3636178 3636178 single base substitution A C intron_variant MELA-AU 16 3636751 3636751 single base substitution G A intron_variant MELA-AU 16 3636806 3636806 single base substitution G A intron_variant MELA-AU 16 3637416 3637416 single base substitution G A intron_variant MELA-AU 16 3637421 3637421 single base substitution C T intron_variant MELA-AU 16 3637982 3637982 single base substitution G A intron_variant MELA-AU 16 3638915 3638915 single base substitution C T intron_variant MELA-AU 16 3639692 3639692 single base substitution G A missense_variant P1316L 3947C>T MELA-AU 16 3639953 3639953 single base substitution A G missense_variant L1229S 3686T>C MELA-AU 16 3639963 3639963 single base substitution G A missense_variant R1226W 3676C>T MELA-AU 16 3639977 3639977 single base substitution G A missense_variant A1221V 3662C>T MELA-AU 16 3640028 3640028 single base substitution G A missense_variant S1204F 3611C>T MELA-AU 16 3640179 3640180 multiple base substitution (>=2bp and <=200bp) AG CA missense_variant LL1153LV MELA-AU 16 3640786 3640786 single base substitution C T downstream_gene_variant MELA-AU 16 3640786 3640786 single base substitution C T synonymous_variant E951E 2853G>A MELA-AU 16 3641049 3641049 single base substitution G A downstream_gene_variant MELA-AU 16 3641049 3641049 single base substitution G A missense_variant L864F 2590C>T MELA-AU 16 3641137 3641137 single base substitution C T downstream_gene_variant MELA-AU 16 3641137 3641137 single base substitution C T synonymous_variant L834L 2502G>A MELA-AU 16 3641593 3641593 single base substitution G A downstream_gene_variant MELA-AU 16 3641593 3641593 single base substitution G A intron_variant MELA-AU 16 3641692 3641692 single base substitution G A downstream_gene_variant MELA-AU 16 3641692 3641692 single base substitution G A intron_variant MELA-AU 16 3641716 3641716 single base substitution G A downstream_gene_variant MELA-AU 16 3641716 3641716 single base substitution G A intron_variant MELA-AU 16 3642161 3642161 single base substitution A T downstream_gene_variant MELA-AU 16 3642161 3642161 single base substitution A T intron_variant MELA-AU 16 3642605 3642605 single base substitution G A downstream_gene_variant MELA-AU 16 3642605 3642605 single base substitution G A intron_variant MELA-AU 16 3642913 3642914 multiple base substitution (>=2bp and <=200bp) AA GT downstream_gene_variant MELA-AU 16 3642913 3642914 multiple base substitution (>=2bp and <=200bp) AA GT intron_variant MELA-AU 16 3643197 3643197 single base substitution C A downstream_gene_variant MELA-AU 16 3643197 3643197 single base substitution C A intron_variant MELA-AU 16 3643376 3643376 single base substitution C T downstream_gene_variant MELA-AU 16 3643376 3643376 single base substitution C T intron_variant MELA-AU 16 3643393 3643393 deletion of <=200bp T - downstream_gene_variant MELA-AU 16 3643393 3643393 deletion of <=200bp T - intron_variant MELA-AU 16 3643575 3643575 single base substitution G A downstream_gene_variant MELA-AU 16 3643575 3643575 single base substitution G A intron_variant MELA-AU 16 3643795 3643795 single base substitution G A downstream_gene_variant MELA-AU 16 3643795 3643795 single base substitution G A intron_variant MELA-AU 16 3643852 3643852 single base substitution G A downstream_gene_variant MELA-AU 16 3643852 3643852 single base substitution G A intron_variant MELA-AU 16 3643862 3643862 single base substitution G A downstream_gene_variant MELA-AU 16 3643862 3643862 single base substitution G A intron_variant MELA-AU 16 3644247 3644247 single base substitution A G downstream_gene_variant MELA-AU 16 3644247 3644247 single base substitution A G intron_variant MELA-AU 16 3644317 3644317 single base substitution A G downstream_gene_variant MELA-AU 16 3644317 3644317 single base substitution A G intron_variant MELA-AU 16 3644326 3644326 single base substitution G A downstream_gene_variant MELA-AU 16 3644326 3644326 single base substitution G A intron_variant MELA-AU 16 3644823 3644823 single base substitution C T downstream_gene_variant MELA-AU 16 3644823 3644823 single base substitution C T intron_variant MELA-AU 16 3644965 3644965 single base substitution G A downstream_gene_variant MELA-AU 16 3644965 3644965 single base substitution G A intron_variant MELA-AU 16 3645064 3645064 single base substitution T C downstream_gene_variant MELA-AU 16 3645064 3645064 single base substitution T C intron_variant MELA-AU 16 3645128 3645128 single base substitution G A downstream_gene_variant MELA-AU 16 3645128 3645128 single base substitution G A intron_variant MELA-AU 16 3645284 3645284 single base substitution G A downstream_gene_variant MELA-AU 16 3645284 3645284 single base substitution G A intron_variant MELA-AU 16 3645364 3645364 single base substitution G A downstream_gene_variant MELA-AU 16 3645364 3645364 single base substitution G A intron_variant MELA-AU 16 3645382 3645382 single base substitution G A downstream_gene_variant MELA-AU 16 3645382 3645382 single base substitution G A intron_variant MELA-AU 16 3647335 3647335 single base substitution A G downstream_gene_variant MELA-AU 16 3647335 3647335 single base substitution A G intron_variant MELA-AU 16 3647339 3647339 insertion of <=200bp - C downstream_gene_variant MELA-AU 16 3647339 3647339 insertion of <=200bp - C intron_variant MELA-AU 16 3647367 3647367 single base substitution G A downstream_gene_variant MELA-AU 16 3647367 3647367 single base substitution G A intron_variant MELA-AU 16 3648025 3648025 single base substitution T C downstream_gene_variant MELA-AU 16 3648025 3648025 single base substitution T C intron_variant MELA-AU 16 3649287 3649287 single base substitution G A downstream_gene_variant MELA-AU 16 3649287 3649287 single base substitution G A intron_variant MELA-AU 16 3649539 3649539 single base substitution A C downstream_gene_variant MELA-AU 16 3649539 3649539 single base substitution A C intron_variant MELA-AU 16 3649695 3649695 single base substitution C T downstream_gene_variant MELA-AU 16 3649695 3649695 single base substitution C T intron_variant MELA-AU 16 3649825 3649825 single base substitution G A downstream_gene_variant MELA-AU 16 3649825 3649825 single base substitution G A intron_variant MELA-AU 16 3650250 3650250 single base substitution G A downstream_gene_variant MELA-AU 16 3650250 3650250 single base substitution G A intron_variant MELA-AU 16 3650817 3650817 single base substitution G A exon_variant MELA-AU 16 3650817 3650817 single base substitution G A intron_variant MELA-AU 16 3650867 3650867 single base substitution G A exon_variant MELA-AU 16 3650867 3650867 single base substitution G A intron_variant MELA-AU 16 3651216 3651216 single base substitution G A exon_variant MELA-AU 16 3651216 3651216 single base substitution G A intron_variant MELA-AU 16 3651218 3651218 single base substitution G A exon_variant MELA-AU 16 3651218 3651218 single base substitution G A intron_variant MELA-AU 16 3651336 3651336 single base substitution C T exon_variant MELA-AU 16 3651336 3651336 single base substitution C T intron_variant MELA-AU 16 3651364 3651364 single base substitution T G exon_variant MELA-AU 16 3651364 3651364 single base substitution T G intron_variant MELA-AU 16 3651393 3651393 single base substitution G A exon_variant MELA-AU 16 3651393 3651393 single base substitution G A intron_variant MELA-AU 16 3651605 3651605 single base substitution G A exon_variant MELA-AU 16 3651605 3651605 single base substitution G A intron_variant MELA-AU 16 3653444 3653444 single base substitution G A intron_variant MELA-AU 16 3653608 3653608 single base substitution A T intron_variant MELA-AU 16 3653624 3653624 single base substitution G A intron_variant MELA-AU 16 3653773 3653788 deletion of <=200bp ATGGGGCACTGTCGCC - intron_variant MELA-AU 16 3654038 3654038 single base substitution C T intron_variant MELA-AU 16 3654347 3654347 single base substitution C T intron_variant MELA-AU 16 3654485 3654485 single base substitution G A intron_variant MELA-AU 16 3654579 3654607 deletion of <=200bp TTTGGGAGACTGAGGTGGACAGATCACAA - intron_variant MELA-AU 16 3654798 3654798 single base substitution G T intron_variant MELA-AU 16 3654800 3654800 single base substitution G A intron_variant MELA-AU 16 3655225 3655225 single base substitution G A intron_variant MELA-AU 16 3655609 3655609 single base substitution G A intron_variant MELA-AU 16 3655724 3655724 single base substitution G A intron_variant MELA-AU 16 3655819 3655819 single base substitution G A intron_variant MELA-AU 16 3655842 3655842 single base substitution G A intron_variant MELA-AU 16 3655861 3655861 single base substitution T C intron_variant MELA-AU 16 3656897 3656898 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 16 3657209 3657209 single base substitution G A intron_variant MELA-AU 16 3657477 3657477 single base substitution A G intron_variant MELA-AU 16 3657497 3657497 single base substitution G A intron_variant MELA-AU 16 3658043 3658043 single base substitution G T intron_variant MELA-AU 16 3658507 3658507 single base substitution G A exon_variant MELA-AU 16 3658507 3658507 single base substitution G A synonymous_variant L153L 459C>T MELA-AU 16 3658524 3658524 single base substitution G A exon_variant MELA-AU 16 3658524 3658524 single base substitution G A missense_variant P148S 442C>T MELA-AU 16 3658588 3658588 single base substitution G A exon_variant MELA-AU 16 3658588 3658588 single base substitution G A synonymous_variant T126T 378C>T MELA-AU 16 3658874 3658874 single base substitution G A exon_variant MELA-AU 16 3658874 3658874 single base substitution G A missense_variant S31F 92C>T MELA-AU 16 3659319 3659319 single base substitution G A 5_prime_UTR_variant MELA-AU 16 3659319 3659319 single base substitution G A exon_variant MELA-AU 16 3659319 3659319 single base substitution G A upstream_gene_variant MELA-AU 16 3659340 3659340 single base substitution C T 5_prime_UTR_variant MELA-AU 16 3659340 3659340 single base substitution C T exon_variant MELA-AU 16 3659340 3659340 single base substitution C T upstream_gene_variant MELA-AU 16 3660287 3660287 single base substitution G A intron_variant MELA-AU 16 3660287 3660287 single base substitution G A upstream_gene_variant MELA-AU 16 3660865 3660865 single base substitution G A intron_variant MELA-AU 16 3660865 3660865 single base substitution G A upstream_gene_variant MELA-AU 16 3662209 3662209 single base substitution G T upstream_gene_variant MELA-AU 16 3662278 3662278 single base substitution T C upstream_gene_variant MELA-AU 16 3662654 3662654 single base substitution C T upstream_gene_variant MELA-AU 16 3663018 3663018 single base substitution T C upstream_gene_variant MELA-AU 16 3663104 3663104 single base substitution C T upstream_gene_variant MELA-AU 16 3663955 3663955 single base substitution C T upstream_gene_variant MELA-AU 16 3664199 3664199 single base substitution C T upstream_gene_variant MELA-AU 16 3664297 3664298 multiple base substitution (>=2bp and <=200bp) TC AT upstream_gene_variant MELA-AU 16 3664410 3664410 single base substitution C T upstream_gene_variant MELA-AU 16 3664773 3664773 single base substitution C T upstream_gene_variant MELA-AU 16 3665296 3665296 single base substitution C T upstream_gene_variant MELA-AU 16 3665317 3665317 single base substitution C T upstream_gene_variant MELA-AU 16 3666425 3666425 single base substitution C T upstream_gene_variant ORCA-IN 16 3639861 3639861 single base substitution T G missense_variant T1260P 3778A>C ORCA-IN 16 3640214 3640214 single base substitution G A missense_variant S1142L 3425C>T ORCA-IN 16 3644233 3644233 single base substitution C T downstream_gene_variant ORCA-IN 16 3644233 3644233 single base substitution C T intron_variant ORCA-IN 16 3644479 3644479 single base substitution G A downstream_gene_variant ORCA-IN 16 3644479 3644479 single base substitution G A missense_variant A712V 2135C>T ORCA-IN 16 3649442 3649442 single base substitution C T downstream_gene_variant ORCA-IN 16 3649442 3649442 single base substitution C T intron_variant ORCA-IN 16 3651142 3651142 single base substitution G C exon_variant ORCA-IN 16 3651142 3651142 single base substitution G C missense_variant P334R 1001C>G ORCA-IN 16 3651157 3651157 single base substitution G T exon_variant ORCA-IN 16 3651157 3651157 single base substitution G T missense_variant S329Y 986C>A ORCA-IN 16 3656692 3656692 single base substitution C A exon_variant ORCA-IN 16 3656692 3656692 single base substitution C A synonymous_variant V181V 543G>T ORCA-IN 16 3658644 3658644 single base substitution C A exon_variant ORCA-IN 16 3658644 3658644 single base substitution C A stop_gained E108* 322G>T ORCA-IN 16 3664848 3664848 single base substitution T C upstream_gene_variant OV-AU 16 3626930 3626930 single base substitution C G downstream_gene_variant OV-AU 16 3630938 3630938 single base substitution G T downstream_gene_variant OV-AU 16 3634510 3634510 single base substitution G A intron_variant OV-AU 16 3635051 3635051 single base substitution G C intron_variant OV-AU 16 3639161 3639161 single base substitution G A missense_variant S1493L 4478C>T OV-AU 16 3640672 3640672 single base substitution T A downstream_gene_variant OV-AU 16 3640672 3640672 single base substitution T A synonymous_variant S989S 2967A>T OV-AU 16 3642768 3642768 single base substitution G C downstream_gene_variant OV-AU 16 3642768 3642768 single base substitution G C missense_variant H753Q 2259C>G OV-AU 16 3647563 3647563 single base substitution C T downstream_gene_variant OV-AU 16 3647563 3647563 single base substitution C T exon_variant OV-AU 16 3647563 3647563 single base substitution C T synonymous_variant T500T 1500G>A OV-AU 16 3647942 3647942 single base substitution G A downstream_gene_variant OV-AU 16 3647942 3647942 single base substitution G A exon_variant OV-AU 16 3647942 3647942 single base substitution G A missense_variant R408W 1222C>T OV-AU 16 3660547 3660547 single base substitution G C intron_variant OV-AU 16 3660547 3660547 single base substitution G C upstream_gene_variant OV-AU 16 3661235 3661235 single base substitution T G intron_variant OV-AU 16 3661235 3661235 single base substitution T G upstream_gene_variant OV-AU 16 3662666 3662666 single base substitution T A upstream_gene_variant OV-AU 16 3663124 3663124 single base substitution G A upstream_gene_variant OV-AU 16 3663234 3663234 single base substitution A G upstream_gene_variant OV-AU 16 3666515 3666515 single base substitution G T upstream_gene_variant OV-AU 16 3666593 3666593 single base substitution G T upstream_gene_variant OV-US 16 3639355 3639355 single base substitution C A missense_variant W1428C 4284G>T OV-US 16 3647922 3647922 single base substitution G A downstream_gene_variant OV-US 16 3647922 3647922 single base substitution G A exon_variant OV-US 16 3647922 3647922 single base substitution G A synonymous_variant D414D 1242C>T PACA-AU 16 3626366 3626366 single base substitution C T downstream_gene_variant PACA-AU 16 3630789 3630789 single base substitution G A downstream_gene_variant PACA-AU 16 3637579 3637579 single base substitution G A intron_variant PACA-AU 16 3640103 3640103 single base substitution T G missense_variant K1179T 3536A>C PACA-AU 16 3641011 3641011 single base substitution G A downstream_gene_variant PACA-AU 16 3641011 3641011 single base substitution G A synonymous_variant D876D 2628C>T PACA-AU 16 3642179 3642179 single base substitution C A downstream_gene_variant PACA-AU 16 3642179 3642179 single base substitution C A intron_variant PACA-AU 16 3647545 3647545 single base substitution G A downstream_gene_variant PACA-AU 16 3647545 3647545 single base substitution G A exon_variant PACA-AU 16 3647545 3647545 single base substitution G A synonymous_variant S506S 1518C>T PACA-AU 16 3647845 3647845 single base substitution G A downstream_gene_variant PACA-AU 16 3647845 3647845 single base substitution G A exon_variant PACA-AU 16 3647845 3647845 single base substitution G A missense_variant A440V 1319C>T PACA-AU 16 3651133 3651133 single base substitution G A exon_variant PACA-AU 16 3651133 3651133 single base substitution G A missense_variant P337L 1010C>T PACA-AU 16 3651383 3651383 single base substitution G C exon_variant PACA-AU 16 3651383 3651383 single base substitution G C intron_variant PACA-AU 16 3653367 3653367 single base substitution A T intron_variant PACA-AU 16 3663433 3663433 single base substitution C A upstream_gene_variant PACA-CA 16 3628695 3628695 single base substitution G C downstream_gene_variant PACA-CA 16 3630604 3630604 single base substitution G A downstream_gene_variant PACA-CA 16 3633865 3633865 single base substitution G A intron_variant PACA-CA 16 3634255 3634255 single base substitution C A intron_variant PACA-CA 16 3635075 3635075 single base substitution C T intron_variant PACA-CA 16 3638360 3638360 single base substitution C T intron_variant PACA-CA 16 3639936 3639936 single base substitution G C missense_variant P1235A 3703C>G PACA-CA 16 3640612 3640612 single base substitution G A downstream_gene_variant PACA-CA 16 3640612 3640612 single base substitution G A synonymous_variant G1009G 3027C>T PACA-CA 16 3641369 3641369 single base substitution C T downstream_gene_variant PACA-CA 16 3641369 3641369 single base substitution C T intron_variant PACA-CA 16 3644934 3644934 single base substitution C A downstream_gene_variant PACA-CA 16 3644934 3644934 single base substitution C A intron_variant PACA-CA 16 3648387 3648387 single base substitution G A downstream_gene_variant PACA-CA 16 3648387 3648387 single base substitution G A intron_variant PACA-CA 16 3648919 3648919 single base substitution C T downstream_gene_variant PACA-CA 16 3648919 3648919 single base substitution C T intron_variant PACA-CA 16 3652236 3652236 single base substitution C T exon_variant PACA-CA 16 3652236 3652236 single base substitution C T missense_variant R278Q 833G>A PACA-CA 16 3652675 3652675 single base substitution C T intron_variant PACA-CA 16 3652700 3652700 single base substitution G A intron_variant PACA-CA 16 3654698 3654698 single base substitution T G intron_variant PACA-CA 16 3663197 3663197 single base substitution G A upstream_gene_variant PACA-CA 16 3664538 3664538 single base substitution A C upstream_gene_variant PBCA-DE 16 3655650 3655650 single base substitution A C intron_variant PRAD-CA 16 3631963 3631963 single base substitution G A 3_prime_UTR_variant PRAD-CA 16 3645415 3645415 single base substitution C T downstream_gene_variant PRAD-CA 16 3645415 3645415 single base substitution C T intron_variant PRAD-UK 16 3633415 3633415 single base substitution G A synonymous_variant D1612D 4836C>T PRAD-UK 16 3635929 3635929 single base substitution G A intron_variant PRAD-UK 16 3660244 3660244 single base substitution A G intron_variant PRAD-UK 16 3660244 3660244 single base substitution A G upstream_gene_variant PRAD-UK 16 3666576 3666576 single base substitution C T upstream_gene_variant PRAD-US 16 3640329 3640329 single base substitution G A missense_variant R1104W 3310C>T PRAD-US 16 3640681 3640681 single base substitution G A downstream_gene_variant PRAD-US 16 3640681 3640681 single base substitution G A synonymous_variant L986L 2958C>T PRAD-US 16 3647657 3647657 deletion of <=200bp G - downstream_gene_variant PRAD-US 16 3647657 3647657 deletion of <=200bp G - exon_variant PRAD-US 16 3647657 3647657 deletion of <=200bp G - frameshift_variant P469 PRAD-US 16 3658496 3658496 single base substitution G A exon_variant PRAD-US 16 3658496 3658496 single base substitution G A missense_variant A157V 470C>T READ-US 16 3639900 3639900 single base substitution C T missense_variant E1247K 3739G>A READ-US 16 3640479 3640479 single base substitution A T missense_variant S1054T 3160T>A RECA-EU 16 3637015 3637015 single base substitution G C intron_variant RECA-EU 16 3641913 3641913 single base substitution T A downstream_gene_variant RECA-EU 16 3641913 3641913 single base substitution T A intron_variant RECA-EU 16 3665408 3665408 single base substitution C T upstream_gene_variant SKCA-BR 16 3626588 3626588 single base substitution C T downstream_gene_variant SKCA-BR 16 3629681 3629681 single base substitution T C downstream_gene_variant SKCA-BR 16 3632298 3632298 single base substitution T G 3_prime_UTR_variant SKCA-BR 16 3632324 3632324 single base substitution T G 3_prime_UTR_variant SKCA-BR 16 3632329 3632329 single base substitution T G 3_prime_UTR_variant SKCA-BR 16 3635586 3635587 deletion of <=200bp CA - intron_variant SKCA-BR 16 3640257 3640257 single base substitution G A stop_gained Q1128* 3382C>T SKCA-BR 16 3643303 3643303 single base substitution G A downstream_gene_variant SKCA-BR 16 3643303 3643303 single base substitution G A intron_variant SKCA-BR 16 3648797 3648797 single base substitution G A downstream_gene_variant SKCA-BR 16 3648797 3648797 single base substitution G A intron_variant SKCA-BR 16 3649945 3649945 single base substitution C T downstream_gene_variant SKCA-BR 16 3649945 3649945 single base substitution C T intron_variant SKCA-BR 16 3650384 3650384 single base substitution G A downstream_gene_variant SKCA-BR 16 3650384 3650384 single base substitution G A intron_variant SKCA-BR 16 3650592 3650600 deletion of <=200bp CTTTTTTTT - downstream_gene_variant SKCA-BR 16 3650592 3650600 deletion of <=200bp CTTTTTTTT - intron_variant SKCA-BR 16 3654249 3654249 single base substitution G A intron_variant SKCA-BR 16 3656406 3656406 single base substitution T C intron_variant SKCA-BR 16 3656478 3656478 single base substitution T C exon_variant SKCA-BR 16 3656478 3656478 single base substitution T C missense_variant N253D 757A>G SKCA-BR 16 3658400 3658400 single base substitution C T intron_variant SKCA-BR 16 3659185 3659185 single base substitution A G 5_prime_UTR_variant SKCA-BR 16 3659185 3659185 single base substitution A G exon_variant SKCA-BR 16 3661373 3661373 single base substitution G C intron_variant SKCA-BR 16 3661373 3661373 single base substitution G C upstream_gene_variant SKCA-BR 16 3661384 3661384 single base substitution A C intron_variant SKCA-BR 16 3661384 3661384 single base substitution A C upstream_gene_variant SKCA-BR 16 3663107 3663107 single base substitution A C upstream_gene_variant SKCA-BR 16 3663231 3663231 single base substitution G A upstream_gene_variant SKCM-US 16 3632512 3632512 single base substitution C T missense_variant R1779Q 5336G>A SKCM-US 16 3632567 3632567 single base substitution G A missense_variant R1761C 5281C>T SKCM-US 16 3632685 3632685 single base substitution G A synonymous_variant S1721S 5163C>T SKCM-US 16 3632689 3632689 single base substitution G A missense_variant S1720F 5159C>T SKCM-US 16 3633161 3633161 single base substitution G A missense_variant P1697L 5090C>T SKCM-US 16 3633209 3633209 single base substitution G A missense_variant S1681L 5042C>T SKCM-US 16 3633257 3633257 single base substitution G A missense_variant P1665L 4994C>T SKCM-US 16 3633395 3633395 single base substitution G A missense_variant P1619L 4856C>T SKCM-US 16 3633422 3633422 single base substitution G A missense_variant S1610F 4829C>T SKCM-US 16 3633495 3633495 single base substitution G A synonymous_variant L1586L 4756C>T SKCM-US 16 3639232 3639232 single base substitution G A synonymous_variant S1469S 4407C>T SKCM-US 16 3639257 3639257 single base substitution G A missense_variant A1461V 4382C>T SKCM-US 16 3639374 3639374 single base substitution G A missense_variant P1422L 4265C>T SKCM-US 16 3639402 3639402 single base substitution G A missense_variant P1413S 4237C>T SKCM-US 16 3639432 3639432 single base substitution C T missense_variant E1403K 4207G>A SKCM-US 16 3639602 3639602 single base substitution G A missense_variant P1346L 4037C>T SKCM-US 16 3639611 3639611 single base substitution G A missense_variant P1343L 4028C>T SKCM-US 16 3639678 3639678 single base substitution G A missense_variant P1321S 3961C>T SKCM-US 16 3639790 3639790 single base substitution G A synonymous_variant A1283A 3849C>T SKCM-US 16 3639858 3639858 single base substitution G A missense_variant P1261S 3781C>T SKCM-US 16 3639925 3639925 single base substitution G A synonymous_variant F1238F 3714C>T SKCM-US 16 3640116 3640116 single base substitution G A missense_variant P1175S 3523C>T SKCM-US 16 3640281 3640281 single base substitution T G missense_variant K1120Q 3358A>C SKCM-US 16 3640456 3640456 single base substitution G A synonymous_variant S1061S 3183C>T SKCM-US 16 3640461 3640461 single base substitution G A missense_variant R1060W 3178C>T SKCM-US 16 3640520 3640520 single base substitution G A missense_variant P1040L 3119C>T SKCM-US 16 3640521 3640521 single base substitution G A missense_variant P1040S 3118C>T SKCM-US 16 3640889 3640889 single base substitution G A downstream_gene_variant SKCM-US 16 3640889 3640889 single base substitution G A missense_variant A917V 2750C>T SKCM-US 16 3640985 3640985 single base substitution G T downstream_gene_variant SKCM-US 16 3640985 3640985 single base substitution G T missense_variant P885Q 2654C>A SKCM-US 16 3641088 3641088 single base substitution T C downstream_gene_variant SKCM-US 16 3641088 3641088 single base substitution T C missense_variant M851V 2551A>G SKCM-US 16 3641157 3641157 single base substitution C T downstream_gene_variant SKCM-US 16 3641157 3641157 single base substitution C T missense_variant E828K 2482G>A SKCM-US 16 3641185 3641185 single base substitution G A downstream_gene_variant SKCM-US 16 3641185 3641185 single base substitution G A synonymous_variant L818L 2454C>T SKCM-US 16 3644580 3644580 single base substitution A C downstream_gene_variant SKCM-US 16 3644580 3644580 single base substitution A C synonymous_variant V678V 2034T>G SKCM-US 16 3645678 3645678 single base substitution G A downstream_gene_variant SKCM-US 16 3645678 3645678 single base substitution G A exon_variant SKCM-US 16 3645678 3645678 single base substitution G A synonymous_variant P647P 1941C>T SKCM-US 16 3652243 3652243 single base substitution A G exon_variant SKCM-US 16 3652243 3652243 single base substitution A G missense_variant F276L 826T>C SKCM-US 16 3656630 3656630 single base substitution T G exon_variant SKCM-US 16 3656630 3656630 single base substitution T G missense_variant K202T 605A>C SKCM-US 16 3658452 3658452 single base substitution G A exon_variant SKCM-US 16 3658452 3658452 single base substitution G A missense_variant L172F 514C>T SKCM-US 16 3658900 3658900 single base substitution G A exon_variant SKCM-US 16 3658900 3658900 single base substitution G A synonymous_variant A22A 66C>T STAD-US 16 3632367 3632367 single base substitution G A synonymous_variant G1827G 5481C>T STAD-US 16 3632513 3632513 single base substitution G A missense_variant R1779W 5335C>T STAD-US 16 3632656 3632656 single base substitution G A missense_variant A1731V 5192C>T STAD-US 16 3633383 3633383 single base substitution G A missense_variant A1623V 4868C>T STAD-US 16 3633486 3633486 single base substitution G A missense_variant R1589C 4765C>T STAD-US 16 3639090 3639090 deletion of <=200bp C - frameshift_variant E1517 STAD-US 16 3639115 3639115 single base substitution C T synonymous_variant S1508S 4524G>A STAD-US 16 3639156 3639156 single base substitution C T missense_variant A1495T 4483G>A STAD-US 16 3639367 3639367 single base substitution G A synonymous_variant D1424D 4272C>T STAD-US 16 3639390 3639390 single base substitution T C missense_variant S1417G 4249A>G STAD-US 16 3639789 3639789 single base substitution C T missense_variant V1284M 3850G>A STAD-US 16 3640167 3640167 single base substitution C T missense_variant D1158N 3472G>A STAD-US 16 3640169 3640169 single base substitution G A missense_variant S1157L 3470C>T STAD-US 16 3640449 3640449 single base substitution C T missense_variant G1064R 3190G>A STAD-US 16 3640516 3640516 single base substitution C T synonymous_variant Q1041Q 3123G>A STAD-US 16 3640549 3640549 single base substitution C T synonymous_variant P1030P 3090G>A STAD-US 16 3640612 3640612 single base substitution G A downstream_gene_variant STAD-US 16 3640612 3640612 single base substitution G A synonymous_variant G1009G 3027C>T STAD-US 16 3640761 3640761 single base substitution T C downstream_gene_variant STAD-US 16 3640761 3640761 single base substitution T C missense_variant S960G 2878A>G STAD-US 16 3640830 3640830 single base substitution C A downstream_gene_variant STAD-US 16 3640830 3640830 single base substitution C A missense_variant G937W 2809G>T STAD-US 16 3640962 3640962 single base substitution C A downstream_gene_variant STAD-US 16 3640962 3640962 single base substitution C A missense_variant G893C 2677G>T STAD-US 16 3641099 3641099 single base substitution T C downstream_gene_variant STAD-US 16 3641099 3641099 single base substitution T C missense_variant N847S 2540A>G STAD-US 16 3641292 3641292 single base substitution C T downstream_gene_variant STAD-US 16 3641292 3641292 single base substitution C T missense_variant V783I 2347G>A STAD-US 16 3644517 3644517 single base substitution G A downstream_gene_variant STAD-US 16 3644517 3644517 single base substitution G A synonymous_variant S699S 2097C>T STAD-US 16 3644567 3644567 single base substitution C T downstream_gene_variant STAD-US 16 3644567 3644567 single base substitution C T missense_variant A683T 2047G>A STAD-US 16 3647811 3647811 single base substitution T C downstream_gene_variant STAD-US 16 3647811 3647811 single base substitution T C exon_variant STAD-US 16 3647811 3647811 single base substitution T C missense_variant I451M 1353A>G STAD-US 16 3647972 3647972 single base substitution G A downstream_gene_variant STAD-US 16 3647972 3647972 single base substitution G A exon_variant STAD-US 16 3647972 3647972 single base substitution G A missense_variant R398W 1192C>T STAD-US 16 3656500 3656500 single base substitution A C exon_variant STAD-US 16 3656500 3656500 single base substitution A C synonymous_variant P245P 735T>G STAD-US 16 3656526 3656526 single base substitution G A exon_variant STAD-US 16 3656526 3656526 single base substitution G A missense_variant R237W 709C>T STAD-US 16 3656564 3656564 single base substitution A G exon_variant STAD-US 16 3656564 3656564 single base substitution A G missense_variant L224S 671T>C STAD-US 16 3656674 3656674 single base substitution C A exon_variant STAD-US 16 3656674 3656674 single base substitution C A missense_variant Q187H 561G>T STAD-US 16 3658536 3658536 single base substitution G A exon_variant STAD-US 16 3658536 3658536 single base substitution G A missense_variant L144F 430C>T STAD-US 16 3658827 3658827 single base substitution A G exon_variant STAD-US 16 3658827 3658827 single base substitution A G missense_variant S47P 139T>C THCA-US 16 3642722 3642722 single base substitution C G downstream_gene_variant THCA-US 16 3642722 3642722 single base substitution C G missense_variant E769Q 2305G>C UCEC-US 16 3633244 3633244 single base substitution C T synonymous_variant R1669R 5007G>A UCEC-US 16 3633501 3633501 single base substitution G A missense_variant R1584C 4750C>T UCEC-US 16 3639062 3639062 single base substitution G T missense_variant P1526H 4577C>A UCEC-US 16 3639255 3639255 single base substitution C T missense_variant A1462T 4384G>A UCEC-US 16 3639605 3639605 single base substitution C T missense_variant R1345H 4034G>A UCEC-US 16 3639963 3639963 single base substitution G A missense_variant R1226W 3676C>T UCEC-US 16 3640455 3640455 single base substitution G A missense_variant R1062C 3184C>T UCEC-US 16 3640473 3640473 deletion of <=200bp G - frameshift_variant L1056 UCEC-US 16 3640577 3640577 single base substitution C T missense_variant R1021H 3062G>A UCEC-US 16 3640795 3640795 single base substitution C T downstream_gene_variant UCEC-US 16 3640795 3640795 single base substitution C T synonymous_variant A948A 2844G>A UCEC-US 16 3641022 3641022 single base substitution C T downstream_gene_variant UCEC-US 16 3641022 3641022 single base substitution C T missense_variant A873T 2617G>A UCEC-US 16 3641150 3641150 single base substitution G A downstream_gene_variant UCEC-US 16 3641150 3641150 single base substitution G A missense_variant A830V 2489C>T UCEC-US 16 3641185 3641185 single base substitution G T downstream_gene_variant UCEC-US 16 3641185 3641185 single base substitution G T synonymous_variant L818L 2454C>A UCEC-US 16 3641251 3641251 single base substitution C A downstream_gene_variant UCEC-US 16 3641251 3641251 single base substitution C A missense_variant E796D 2388G>T UCEC-US 16 3641304 3641304 single base substitution C T downstream_gene_variant UCEC-US 16 3641304 3641304 single base substitution C T missense_variant V779M 2335G>A UCEC-US 16 3642849 3642849 single base substitution G T downstream_gene_variant UCEC-US 16 3642849 3642849 single base substitution G T missense_variant F726L 2178C>A UCEC-US 16 3644469 3644469 single base substitution C T downstream_gene_variant UCEC-US 16 3644469 3644469 single base substitution C T synonymous_variant P715P 2145G>A UCEC-US 16 3645678 3645678 single base substitution G A downstream_gene_variant UCEC-US 16 3645678 3645678 single base substitution G A exon_variant UCEC-US 16 3645678 3645678 single base substitution G A synonymous_variant P647P 1941C>T UCEC-US 16 3645687 3645687 single base substitution G A downstream_gene_variant UCEC-US 16 3645687 3645687 single base substitution G A exon_variant UCEC-US 16 3645687 3645687 single base substitution G A synonymous_variant D644D 1932C>T UCEC-US 16 3647549 3647549 single base substitution G A downstream_gene_variant UCEC-US 16 3647549 3647549 single base substitution G A exon_variant UCEC-US 16 3647549 3647549 single base substitution G A missense_variant A505V 1514C>T UCEC-US 16 3647844 3647844 single base substitution C T downstream_gene_variant UCEC-US 16 3647844 3647844 single base substitution C T exon_variant UCEC-US 16 3647844 3647844 single base substitution C T synonymous_variant A440A 1320G>A UCEC-US 16 3647887 3647887 single base substitution G T downstream_gene_variant UCEC-US 16 3647887 3647887 single base substitution G T exon_variant UCEC-US 16 3647887 3647887 single base substitution G T missense_variant A426D 1277C>A UCEC-US 16 3652147 3652147 single base substitution C T exon_variant UCEC-US 16 3652147 3652147 single base substitution C T missense_variant V308M 922G>A UCEC-US 16 3652166 3652166 single base substitution C A exon_variant UCEC-US 16 3652166 3652166 single base substitution C A missense_variant K301N 903G>T UCEC-US 16 3656556 3656556 single base substitution C T exon_variant UCEC-US 16 3656556 3656556 single base substitution C T missense_variant A227T 679G>A UCEC-US 16 3656624 3656624 single base substitution C T exon_variant UCEC-US 16 3656624 3656624 single base substitution C T missense_variant R204H 611G>A UCEC-US 16 3658509 3658509 single base substitution G T exon_variant UCEC-US 16 3658509 3658509 single base substitution G T missense_variant L153I 457C>A UCEC-US 16 3658582 3658582 single base substitution C T exon_variant UCEC-US 16 3658582 3658582 single base substitution C T stop_gained W128* 384G>A UCEC-US 16 3658652 3658652 single base substitution C A exon_variant UCEC-US 16 3658652 3658652 single base substitution C A missense_variant G105V 314G>T UCEC-US 16 3658963 3658963 single base substitution C A exon_variant UCEC-US 16 3658963 3658963 single base substitution C A start_lost M1I 3G>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-BH-A1F2-01 COSM1478863 c.2542G>A p.E848K Substitution - Missense 16:3591096-3591096 - CSCC-32-T COSM4477991 c.2200C>T p.L734L Substitution - coding silent 16:3592826-3592826 - MedB-1 COSM5621864 c.265A>G p.K89E Substitution - Missense 16:3608700-3608700 - TCGA-24-1470-01 COSM76523 c.4284G>T p.W1428C Substitution - Missense 16:3589354-3589354 - PT53 COSM5941394 c.4490C>T p.S1497F Substitution - Missense 16:3589148-3589148 - TCGA-D3-A51T-06 COSM3509531 c.3183C>T p.S1061S Substitution - coding silent 16:3590455-3590455 - LUAD-E01317 COSM403692 c.416G>T p.G139V Substitution - Missense 16:3608549-3608549 - JEKO-1 COSM1740291 c.1183G>T p.G395C Substitution - Missense 16:3597980-3597980 - CSCC-27-T COSM4486458 c.3056C>G p.S1019C Substitution - Missense 16:3590582-3590582 - CCK81 COSM2919766 c.1511C>A p.P504H Substitution - Missense 16:3597551-3597551 - TCGA-HU-A4G9-01 COSM4060661 c.2347G>A p.V783I Substitution - Missense 16:3591291-3591291 - S0080 COSM5882711 c.3004A>G p.S1002G Substitution - Missense 16:3590634-3590634 - YUVEME COSM5384868 c.460C>T p.R154W Substitution - Missense 16:3608505-3608505 - 587242 COSM1185021 c.3850G>A p.V1284M Substitution - Missense 16:3589788-3589788 - TCGA-BS-A0UV-01 COSM970503 c.903G>T p.K301N Substitution - Missense 16:3602165-3602165 - TCGA-BR-4362-01 COSM4060659 c.2677G>T p.G893C Substitution - Missense 16:3590961-3590961 - TCGA-BS-A0UL-01 COSM970504 c.679G>A p.A227T Substitution - Missense 16:3606555-3606555 - HCC2998 COSM1678803 c.4523C>T p.S1508L Substitution - Missense 16:3589115-3589115 - TCGA-AX-A05Z-01 COSM970509 c.3G>T p.M1I Substitution - Missense 16:3608962-3608962 - HDC87 COSM4636952 c.2142C>T p.C714C Substitution - coding silent 16:3594471-3594471 - B89-4 COSM1749595 c.3234G>C p.V1078V Substitution - coding silent 16:3590404-3590404 - T2269 COSM4728188 c.4951C>T p.P1651S Substitution - Missense 16:3583299-3583299 - TCGA-39-5031-01 COSM703056 c.5101G>C p.E1701Q Substitution - Missense 16:3583149-3583149 - sysucc-1317T COSM5448867 c.3059A>G p.H1020R Substitution - Missense 16:3590579-3590579 - PD13623a COSM263758 c.3631G>A p.E1211K Substitution - Missense 16:3590007-3590007 - TCGA-GV-A3QH-01 COSM1301950 c.3661G>T p.A1221S Substitution - Missense 16:3589977-3589977 - TCGA-EB-A299-01 COSM3509537 c.2482G>A p.E828K Substitution - Missense 16:3591156-3591156 - ESO-610 COSM1246292 c.2242G>A p.A748T Substitution - Missense 16:3592784-3592784 - PD5935a COSM5771986 c.3584T>C p.I1195T Substitution - Missense 16:3590054-3590054 - 0007_CRUK_PC_0007_T1_DNA COSM3849553 c.4836C>T p.D1612D Substitution - coding silent 16:3583414-3583414 - TCGA-D1-A17D-01 COSM970482 c.3401C>T p.S1134L Substitution - Missense 16:3590237-3590237 - T276 COSM2919687 c.3913G>A p.A1305T Substitution - Missense 16:3589725-3589725 - 113368 COSM324837 c.4894C>T p.Q1632* Substitution - Nonsense 16:3583356-3583356 - TCGA-AP-A059-01 COSM970506 c.457C>A p.L153I Substitution - Missense 16:3608508-3608508 - RK035_C01 COSM1629889 c.4401T>C p.C1467C Substitution - coding silent 16:3589237-3589237 - T3225 COSM4728186 c.5246C>T p.A1749V Substitution - Missense 16:3582601-3582601 - TCGA-D1-A174-01 COSM970502 c.922G>A p.V308M Substitution - Missense 16:3602146-3602146 - WA33 COSM238211 c.1443A>G p.R481R Substitution - coding silent 16:3597619-3597619 - BD121T COSM5515583 c.190A>C p.K64Q Substitution - Missense 16:3608775-3608775 - TCGA-B5-A0JY-01 COSM970493 c.2178C>A p.F726L Substitution - Missense 16:3592848-3592848 - TCGA-06-2567 COSM2153065 c.3772_3774delCCC p.P1258delP Deletion - In frame 16:3589864-3589866 - TCGA-BG-A0VZ-01 COSM970499 c.1514C>T p.A505V Substitution - Missense 16:3597548-3597548 - TCGA-06-0122 COSM1246293 c.2193C>T p.D731D Substitution - coding silent 16:3592833-3592833 - RK048_C COSM1629890 c.795C>T p.D265D Substitution - coding silent 16:3602273-3602273 - AOCS-139-6-3 COSM3948538 c.2967A>T p.S989S Substitution - coding silent 16:3590671-3590671 - 2011-2322:2012-352-T COSM4605151 c.335C>T p.P112L Substitution - Missense 16:3608630-3608630 - OSCC-GB_00540111 COSM4889515 c.3778A>C p.T1260P Substitution - Missense 16:3589860-3589860 - 587338 COSM1185023 c.2090C>T p.T697M Substitution - Missense 16:3594523-3594523 - TCGA-D1-A17D-01 COSM970494 c.2145G>A p.P715P Substitution - coding silent 16:3594468-3594468 - pfg019T COSM1640476 c.2628C>T p.D876D Substitution - coding silent 16:3591010-3591010 - TCGA-D3-A51J-06 COSM3509522 c.4265C>T p.P1422L Substitution - Missense 16:3589373-3589373 - TCGA-D9-A6EC-06 COSM4405026 c.605A>C p.K202T Substitution - Missense 16:3606629-3606629 - TCGA-CM-6674-01 COSM970481 c.3676C>T p.R1226W Substitution - Missense 16:3589962-3589962 - TCGA-FW-A3R5-06 COSM3888512 c.3849C>T p.A1283A Substitution - coding silent 16:3589789-3589789 - TCGA-AA-A010-01 COSM285188 c.2439G>T p.E813D Substitution - Missense 16:3591199-3591199 - TCGA-A6-6140-01 COSM3754891 c.2855C>T p.A952V Substitution - Missense 16:3590783-3590783 - TCGA-AA-3715-01 COSM270195 c.4339G>T p.G1447C Substitution - Missense 16:3589299-3589299 - BD72T COSM5513158 c.2779G>A p.A927T Substitution - Missense 16:3590859-3590859 - TCGA-18-3409-01 COSM703054 c.4258C>T p.P1420S Substitution - Missense 16:3589380-3589380 - TCGA-B0-5092-01 COSM471704 c.2982C>A p.I994I Substitution - coding silent 16:3590656-3590656 - TCGA-FS-A1ZZ-06 COSM3509530 c.3523C>T p.P1175S Substitution - Missense 16:3590115-3590115 - QC2-32-T2 COSM3679905 c.3868C>A p.H1290N Substitution - Missense 16:3589770-3589770 - CHC2048T COSM4793116 c.1156A>G p.M386V Substitution - Missense 16:3600986-3600986 - AOCS-061-1-8 COSM3948540 c.1500G>A p.T500T Substitution - coding silent 16:3597562-3597562 - TCGA-A7-A0CJ-01 COSM5833081 c.5325_5326insC p.F1776fs*2 Insertion - Frameshift 16:3582521-3582522 - SNU-175 COSM2919708 c.3308G>A p.R1103H Substitution - Missense 16:3590330-3590330 - T3021 COSM4728190 c.4333C>T p.R1445W Substitution - Missense 16:3589305-3589305 - TCGA-G9-6365-01 COSM1128964 c.470C>T p.A157V Substitution - Missense 16:3608495-3608495 - TCGA-A6-5665-01 COSM1377787 c.921C>T p.N307N Substitution - coding silent 16:3602147-3602147 - 587332 COSM1185024 c.2398T>C p.W800R Substitution - Missense 16:3591240-3591240 - D28 COSM5545847 c.1587T>C p.F529F Substitution - coding silent 16:3597475-3597475 - J83_T COSM3957558 c.2246G>T p.R749L Substitution - Missense 16:3592780-3592780 - Gp2D COSM2919726 c.2874C>T p.C958C Substitution - coding silent 16:3590764-3590764 - TCGA-B7-5816-01 COSM4060646 c.4868C>T p.A1623V Substitution - Missense 16:3583382-3583382 - TCGA-BR-4368-01 COSM4060655 c.3123G>A p.Q1041Q Substitution - coding silent 16:3590515-3590515 - T3262 COSM2919723 c.2990C>T p.P997L Substitution - Missense 16:3590648-3590648 - TCGA-D1-A167-01 COSM970479 c.4384G>A p.A1462T Substitution - Missense 16:3589254-3589254 - S02139 COSM5674209 c.1477G>T p.E493* Substitution - Nonsense 16:3597585-3597585 - T368 COSM4060649 c.4483G>A p.A1495T Substitution - Missense 16:3589155-3589155 - 408 COSM4430412 c.2807C>T p.S936L Substitution - Missense 16:3590831-3590831 - TCGA-BR-6452-01 COSM4060669 c.139T>C p.S47P Substitution - Missense 16:3608826-3608826 - TCGA-D3-A2JH-06 COSM3509520 c.4756C>T p.L1586L Substitution - coding silent 16:3583494-3583494 - RK059_C01 COSM3741917 c.417G>A p.G139G Substitution - coding silent 16:3608548-3608548 - TCGA-EE-A2GC-06 COSM3509527 c.3961C>T p.P1321S Substitution - Missense 16:3589677-3589677 - BCM321T COSM4955234 c.635G>A p.R212Q Substitution - Missense 16:3606599-3606599 - TCGA-EE-A3AB-06 COSM3509515 c.5281C>T p.R1761C Substitution - Missense 16:3582566-3582566 - OSCC-GB_01160111 COSM5956046 c.986C>A p.S329Y Substitution - Missense 16:3601156-3601156 - TCGA-CG-4476-01 COSM4060664 c.1192C>T p.R398W Substitution - Missense 16:3597971-3597971 - C658 COSM178753 c.485C>T p.T162M Substitution - Missense 16:3608480-3608480 - Gp5D COSM2919726 c.2874C>T p.C958C Substitution - coding silent 16:3590764-3590764 - TCGA-E2-A1IJ-01 COSM1478864 c.672G>T p.L224F Substitution - Missense 16:3606562-3606562 - 93T COSM109294 c.3848C>T p.A1283V Substitution - Missense 16:3589790-3589790 - TCGA-AP-A0LD-01 COSM970500 c.1320G>A p.A440A Substitution - coding silent 16:3597843-3597843 - SNUH_G10_S1 COSM3999860 c.753G>C p.A251A Substitution - coding silent 16:3606481-3606481 - T2269 COSM4728192 c.3246G>A p.Q1082Q Substitution - coding silent 16:3590392-3590392 - T2269 COSM1678803 c.4523C>T p.S1508L Substitution - Missense 16:3589115-3589115 - CHC1715T COSM4789510 c.3629G>A p.S1210N Substitution - Missense 16:3590009-3590009 - 2492729 COSM5725853 c.2273C>T p.A758V Substitution - Missense 16:3592753-3592753 - TCGA-EB-A5UN-06 COSM2919673 c.4407C>T p.S1469S Substitution - coding silent 16:3589231-3589231 - OSCC-GB_00990111 COSM4885730 c.2135C>T p.A712V Substitution - Missense 16:3594478-3594478 - TCGA-D9-A6EC-06 COSM4406079 c.3358A>C p.K1120Q Substitution - Missense 16:3590280-3590280 - ME009T COSM223823 c.1153C>T p.P385S Substitution - Missense 16:3600989-3600989 - TCGA-61-1910-01 COSM1324461 c.4227C>G p.A1409A Substitution - coding silent 16:3589411-3589411 - 8035735 COSM1640476 c.2628C>T p.D876D Substitution - coding silent 16:3591010-3591010 - LUAD-RT-S01777 COSM381970 c.2856G>T p.A952A Substitution - coding silent 16:3590782-3590782 - TCGA-CJ-5676-01 COSM471705 c.2469G>A p.W823* Substitution - Nonsense 16:3591169-3591169 - TCGA-D8-A1J8-01 COSM3817957 c.106G>A p.E36K Substitution - Missense 16:3608859-3608859 - 064 COSM1741258 c.926C>A p.T309N Substitution - Missense 16:3602142-3602142 - CHC1742T COSM4792210 c.2147T>G p.L716R Substitution - Missense 16:3594466-3594466 - TCGA-FD-A3SS-01 COSM3794846 c.2848G>C p.E950Q Substitution - Missense 16:3590790-3590790 - 49M COSM5593208 c.3161C>T p.S1054L Substitution - Missense 16:3590477-3590477 - PD4937a COSM159429 c.1368G>C p.E456D Substitution - Missense 16:3597694-3597694 - CSCC-38-T COSM4490722 c.3683C>T p.S1228F Substitution - Missense 16:3589955-3589955 - CSCC-29-T COSM4260226 c.2124C>T p.F708F Substitution - coding silent 16:3594489-3594489 - CSCC-56-T COSM4465869 c.1403C>T p.P468L Substitution - Missense 16:3597659-3597659 - 19 COSM5747699 c.892A>T p.I298F Substitution - Missense 16:3602176-3602176 - COLO201 COSM2919776 c.1179T>C p.S393S Substitution - coding silent 16:3597984-3597984 - 2492726 COSM4465869 c.1403C>T p.P468L Substitution - Missense 16:3597659-3597659 - 855_CLM COSM5754853 c.4096C>T p.R1366C Substitution - Missense 16:3589542-3589542 - cSCCP5 COSM138070 c.5371C>T p.R1791C Substitution - Missense 16:3582476-3582476 - TCGA-AX-A064-01 COSM970491 c.2388G>T p.E796D Substitution - Missense 16:3591250-3591250 - TCGA-AG-A002-01 COSM263758 c.3631G>A p.E1211K Substitution - Missense 16:3590007-3590007 - TCGA-61-2614-01 COSM1324457 c.709C>T p.R237W Substitution - Missense 16:3606525-3606525 - T3202 COSM4728195 c.800C>T p.A267V Substitution - Missense 16:3602268-3602268 - TCGA-22-5482-01 COSM703045 c.518C>G p.S173C Substitution - Missense 16:3608447-3608447 - TCGA-EE-A2A2-06 COSM3509533 c.3118C>T p.P1040S Substitution - Missense 16:3590520-3590520 - CSCC-4-T COSM4532472 c.1888G>A p.G630S Substitution - Missense 16:3596189-3596189 - TCGA-BT-A0YX-01 COSM417012 c.688G>A p.E230K Substitution - Missense 16:3606546-3606546 - CSCC-38-T COSM4566819 c.4814_4815CC>TT p.T1605I Substitution - Missense 16:3583435-3583436 - TCGA-D5-6540-01 COSM1324457 c.709C>T p.R237W Substitution - Missense 16:3606525-3606525 - TCGA-EE-A29Q-06 COSM3509538 c.2454C>T p.L818L Substitution - coding silent 16:3591184-3591184 - T3021 COSM4728187 c.5033delC p.P1678fs*37 Deletion - Frameshift 16:3583217-3583217 - CHC805T COSM4954349 c.1763A>G p.H588R Substitution - Missense 16:3596314-3596314 - TCGA-EK-A3GK-01 COSM4853465 c.614C>T p.T205I Substitution - Missense 16:3606620-3606620 - CCK81 COSM2919763 c.1611T>C p.T537T Substitution - coding silent 16:3597451-3597451 - 2492701 COSM5600528 c.976C>T p.L326L Substitution - coding silent 16:3601166-3601166 - OSCC-GB_01040111 COSM4886127 c.543G>T p.V181V Substitution - coding silent 16:3606691-3606691 - ME100L COSM231337 c.4217C>T p.S1406F Substitution - Missense 16:3589421-3589421 - TCGA-FW-A3R5-06 COSM3888513 c.2750C>T p.A917V Substitution - Missense 16:3590888-3590888 - TCGA-A8-A09Z-01 COSM3817956 c.3800G>A p.R1267H Substitution - Missense 16:3589838-3589838 - TCGA-BR-8487-01 COSM2919752 c.2097C>T p.S699S Substitution - coding silent 16:3594516-3594516 - T2949 COSM4728191 c.3669G>A p.P1223P Substitution - coding silent 16:3589969-3589969 - C086 COSM5539400 c.5400C>T p.F1800F Substitution - coding silent 16:3582447-3582447 - TCGA-BR-4256-01 COSM4060665 c.735T>G p.P245P Substitution - coding silent 16:3606499-3606499 - HCC107 COSM1609316 c.4584C>A p.A1528A Substitution - coding silent 16:3589054-3589054 - SJACT007_D COSM4968087 c.2243C>T p.A748V Substitution - Missense 16:3592783-3592783 - B78 COSM1749596 c.1044C>A p.S348R Substitution - Missense 16:3601098-3601098 - TCGA-CG-4436-01 COSM4060648 c.4524G>A p.S1508S Substitution - coding silent 16:3589114-3589114 - TARGET-30-PAPBJE COSM1283690 c.1098C>T p.L366L Substitution - coding silent 16:3601044-3601044 - TCGA-EE-A2MS-06 COSM3509528 c.3781C>T p.P1261S Substitution - Missense 16:3589857-3589857 - TCGA-BW-A5NP-01 COSM4942679 c.2288C>A p.P763H Substitution - Missense 16:3592738-3592738 - TCGA-K4-A3WV-01 COSM3794845 c.5015A>G p.H1672R Substitution - Missense 16:3583235-3583235 - TCGA-DH-5140-01 COSM3969559 c.2949C>T p.Y983Y Substitution - coding silent 16:3590689-3590689 - Sample_1 COSM5021853 c.3365C>T p.P1122L Substitution - Missense 16:3590273-3590273 - 2492725 COSM4465869 c.1403C>T p.P468L Substitution - Missense 16:3597659-3597659 - PTC-7C COSM4129051 c.3942G>A p.Q1314Q Substitution - coding silent 16:3589696-3589696 - TCGA-22-5473-01 COSM703049 c.2521G>C p.E841Q Substitution - Missense 16:3591117-3591117 - SNU-C2B COSM2919767 c.1499C>T p.T500M Substitution - Missense 16:3597563-3597563 - 8061176 COSM3387433 c.1010C>T p.P337L Substitution - Missense 16:3601132-3601132 - OSCC-GB_00070111 COSM3711925 c.3425C>T p.S1142L Substitution - Missense 16:3590213-3590213 - TCGA-HR-A2OG-01 COSM3509534 c.2918C>T p.S973F Substitution - Missense 16:3590720-3590720 - TCGA-AG-A002-01 COSM263759 c.3027C>T p.G1009G Substitution - coding silent 16:3590611-3590611 - 10 COSM327521 c.4019A>G p.H1340R Substitution - Missense 16:3589619-3589619 - YUMER COSM1708686 c.2143C>T p.P715S Substitution - Missense 16:3594470-3594470 - TCGA-HU-A4GT-01 COSM4060653 c.3470C>T p.S1157L Substitution - Missense 16:3590168-3590168 - TCGA-CA-6717-01 COSM285188 c.2439G>T p.E813D Substitution - Missense 16:3591199-3591199 - CSCC-16-T COSM970496 c.1941C>T p.P647P Substitution - coding silent 16:3595677-3595677 - TCGA-AD-6889-01 COSM1377765 c.5382G>A p.S1794S Substitution - coding silent 16:3582465-3582465 - TCGA-EI-7004-01 COSM3420979 c.3739G>A p.E1247K Substitution - Missense 16:3589899-3589899 - 587376 COSM1185026 c.2911G>T p.E971* Substitution - Nonsense 16:3590727-3590727 - COLO205 COSM2919776 c.1179T>C p.S393S Substitution - coding silent 16:3597984-3597984 - TCGA-HU-A4GU-01 COSM263759 c.3027C>T p.G1009G Substitution - coding silent 16:3590611-3590611 - TCGA-06-0122-01 COSM1246293 c.2193C>T p.D731D Substitution - coding silent 16:3592833-3592833 - TCGA-HU-A4GQ-01 COSM4060647 c.4765C>T p.R1589C Substitution - Missense 16:3583485-3583485 - ccRCC-77 COSM1664262 c.3584T>A p.I1195N Substitution - Missense 16:3590054-3590054 - MAVER-1 COSM1740251 c.2120A>C p.K707T Substitution - Missense 16:3594493-3594493 - TCGA-Q1-A5R1-01 COSM4818714 c.5165G>C p.C1722S Substitution - Missense 16:3582682-3582682 - TCGA-FS-A1ZW-06 COSM3509526 c.4028C>T p.P1343L Substitution - Missense 16:3589610-3589610 - TCGA-EE-A2GI-06 COSM328363 c.3178C>T p.R1060W Substitution - Missense 16:3590460-3590460 - U031 COSM1683098 c.1415T>C p.L472S Substitution - Missense 16:3597647-3597647 - YUGURT COSM5384864 c.3198C>T p.S1066S Substitution - coding silent 16:3590440-3590440 - Pat_46_B COSM5850885 c.3125G>A p.G1042D Substitution - Missense 16:3590513-3590513 - TCGA-HT-A5RB-01 COSM2919722 c.3012C>T p.P1004P Substitution - coding silent 16:3590626-3590626 - RKO COSM4647924 c.4016G>A p.G1339D Substitution - Missense 16:3589622-3589622 - CSCC-31-T COSM4486964 c.3121C>T p.Q1041* Substitution - Nonsense 16:3590517-3590517 - TCGA-A6-3808-01 COSM291356 c.1458T>A p.R486R Substitution - coding silent 16:3597604-3597604 - B78-Tumor COSM1749596 c.1044C>A p.S348R Substitution - Missense 16:3601098-3601098 - TCGA-EE-A2MQ-06 COSM3509535 c.2654C>A p.P885Q Substitution - Missense 16:3590984-3590984 - TCGA-D1-A16F-01 COSM970487 c.2844G>A p.A948A Substitution - coding silent 16:3590794-3590794 - CSCC-7-T COSM4486837 c.3105C>T p.F1035F Substitution - coding silent 16:3590533-3590533 - TCGA-A6-5665-01 COSM1377770 c.4241delC p.P1414fs*36 Deletion - Frameshift 16:3589397-3589397 - TCGA-BR-6452-01 COSM4060644 c.5481C>T p.G1827G Substitution - coding silent 16:3582366-3582366 - WA48 COSM241691 c.413_420delATGGGGAG p.N138fs*24 Deletion - Frameshift 16:3608545-3608552 - T23 COSM5619099 c.5424C>T p.F1808F Substitution - coding silent 16:3582423-3582423 - CSCC-27-T COSM4467119 c.1471C>T p.L491F Substitution - Missense 16:3597591-3597591 - sysucc-1397T COSM4955234 c.635G>A p.R212Q Substitution - Missense 16:3606599-3606599 - TCGA-AA-A010-01 COSM285187 c.2991G>A p.P997P Substitution - coding silent 16:3590647-3590647 - I2L-P11-Tumor-Organoid COSM5363302 c.2083T>A p.F695I Substitution - Missense 16:3594530-3594530 - PR-00-1165 COSM243257 c.5032C>T p.P1678S Substitution - Missense 16:3583218-3583218 - PD9756a COSM5776044 c.1808C>T p.S603L Substitution - Missense 16:3596269-3596269 - Pat_65_A COSM5850886 c.2518G>A p.E840K Substitution - Missense 16:3591120-3591120 - TCGA-CA-6718-01 COSM1377776 c.2906G>T p.R969I Substitution - Missense 16:3590732-3590732 - XHDG20C COSM2919696 c.3583_3585delATT p.I1195delI Deletion - In frame 16:3590053-3590055 - ESCC_29 COSM5627479 c.5117C>T p.S1706F Substitution - Missense 16:3583133-3583133 - AOCS-141-3-2 COSM3948541 c.1222C>T p.R408W Substitution - Missense 16:3597941-3597941 - CHC1715T COSM4789510 c.3629G>A p.S1210N Substitution - Missense 16:3590009-3590009 - TCGA-DD-A1E9-01 COSM4912435 c.4681A>G p.T1561A Substitution - Missense 16:3584827-3584827 - Pat_60_B COSM5740543 c.1232G>A p.R411Q Substitution - Missense 16:3597931-3597931 - TCGA-BR-6452-01 COSM4060666 c.671T>C p.L224S Substitution - Missense 16:3606563-3606563 - 2521252 COSM5889315 c.3515C>T p.S1172F Substitution - Missense 16:3590123-3590123 - 46M COSM5588981 c.5017G>A p.E1673K Substitution - Missense 16:3583233-3583233 - TCGA-BR-8487-01 COSM4060650 c.4272C>T p.D1424D Substitution - coding silent 16:3589366-3589366 - TCGA-30-1718-01 COSM1324460 c.3648G>C p.Q1216H Substitution - Missense 16:3589990-3589990 - CSCC-31-T COSM4560521 c.846G>C p.S282S Substitution - coding silent 16:3602222-3602222 - TCGA-CH-5737-01 COSM1128965 c.2958C>T p.L986L Substitution - coding silent 16:3590680-3590680 - Au4 COSM3509521 c.4382C>T p.A1461V Substitution - Missense 16:3589256-3589256 - HCA7 COSM4630213 c.1110T>A p.A370A Substitution - coding silent 16:3601032-3601032 - TCGA-AP-A0LM-01 COSM970501 c.1277C>A p.A426D Substitution - Missense 16:3597886-3597886 - BD72T COSM5513157 c.2940C>T p.A980A Substitution - coding silent 16:3590698-3590698 - TCGA-AP-A051-01 COSM970489 c.2489C>T p.A830V Substitution - Missense 16:3591149-3591149 - 855_PT COSM5754853 c.4096C>T p.R1366C Substitution - Missense 16:3589542-3589542 - PT45 COSM5927763 c.5030C>T p.P1677L Substitution - Missense 16:3583220-3583220 - 0007_CRUK_PC_0007_T2_DNA COSM3849553 c.4836C>T p.D1612D Substitution - coding silent 16:3583414-3583414 - YURKEN COSM1708688 c.1250C>T p.P417L Substitution - Missense 16:3597913-3597913 - TCGA-EE-A2MR-06 COSM3509532 c.3119C>T p.P1040L Substitution - Missense 16:3590519-3590519 - C086 COSM5539401 c.5139C>T p.S1713S Substitution - coding silent 16:3583111-3583111 - TCGA-AA-3715-01 COSM270196 c.553G>T p.D185Y Substitution - Missense 16:3606681-3606681 - CSCC-11-T COSM3509528 c.3781C>T p.P1261S Substitution - Missense 16:3589857-3589857 - 8044436 COSM3387431 c.1518C>T p.S506S Substitution - coding silent 16:3597544-3597544 - ESO-963 COSM1246293 c.2193C>T p.D731D Substitution - coding silent 16:3592833-3592833 - AOCS-139-19-0 COSM3948538 c.2967A>T p.S989S Substitution - coding silent 16:3590671-3590671 - PTC-7C COSM4129050 c.3943A>G p.T1315A Substitution - Missense 16:3589695-3589695 - TCGA-EE-A3AA-06 COSM2919656 c.4856C>T p.P1619L Substitution - Missense 16:3583394-3583394 - TCGA-37-3789-01 COSM703055 c.4803C>A p.Y1601* Substitution - Nonsense 16:3583447-3583447 - I2L-P7-Tumor-Organoid COSM5363255 c.4668delC p.V1558fs*3 Deletion - Frameshift 16:3584840-3584840 - TCGA-CG-5721-01 COSM4060657 c.2878A>G p.S960G Substitution - Missense 16:3590760-3590760 - AOCS-135-8-X COSM3948539 c.2259C>G p.H753Q Substitution - Missense 16:3592767-3592767 - TCGA-GN-A269-01 COSM3509525 c.4037C>T p.P1346L Substitution - Missense 16:3589601-3589601 - SS6003320 COSM3983073 c.4480G>A p.G1494S Substitution - Missense 16:3589158-3589158 - TCGA-DK-A1AC-01 COSM1301953 c.2449G>A p.E817K Substitution - Missense 16:3591189-3591189 - 2217540 COSM4421444 c.4862_4863delTG p.L1621fs*34 Deletion - Frameshift 16:3583387-3583388 - BD165T COSM5505891 c.3873G>A p.T1291T Substitution - coding silent 16:3589765-3589765 - TCGA-EB-A41A-01 COSM3509529 c.3714C>T p.F1238F Substitution - coding silent 16:3589924-3589924 - TCGA-AP-A0LM-01 COSM970484 c.3184C>T p.R1062C Substitution - Missense 16:3590454-3590454 - S02292 COSM5687507 c.3122A>G p.Q1041R Substitution - Missense 16:3590516-3590516 - 381_T COSM2919685 c.3950C>T p.P1317L Substitution - Missense 16:3589688-3589688 - 442 COSM4434617 c.3895_3896delAG p.R1299fs*35 Deletion - Frameshift 16:3589742-3589743 - TCGA-EI-6513-01 COSM3420980 c.3160T>A p.S1054T Substitution - Missense 16:3590478-3590478 - HCC120T COSM3716919 c.4636+5G>A p.? Unknown 16:3588997-3588997 - TCGA-A7-A0DA-01 COSM435231 c.5426C>G p.T1809S Substitution - Missense 16:3582421-3582421 - DN14042 COSM5962524 c.4857G>A p.P1619P Substitution - coding silent 16:3583393-3583393 - 3498_T COSM3957560 c.209T>A p.V70E Substitution - Missense 16:3608756-3608756 - TCGA-DA-A1I4-06 COSM3509539 c.2034T>G p.V678V Substitution - coding silent 16:3594579-3594579 - BCM321T COSM4955234 c.635G>A p.R212Q Substitution - Missense 16:3606599-3606599 - PR-00-1165 COSM243256 c.832C>T p.R278W Substitution - Missense 16:3602236-3602236 - ASHPC_0010_Pa_P COSM263759 c.3027C>T p.G1009G Substitution - coding silent 16:3590611-3590611 - 587350 COSM1185025 c.3179G>A p.R1060Q Substitution - Missense 16:3590459-3590459 - SNUH_G16_S1 COSM3679905 c.3868C>A p.H1290N Substitution - Missense 16:3589770-3589770 - PT25 COSM5905044 c.763T>A p.Y255N Substitution - Missense 16:3602305-3602305 - 2492700 COSM5600528 c.976C>T p.L326L Substitution - coding silent 16:3601166-3601166 - TCGA-BR-8680-01 COSM4060662 c.2047G>A p.A683T Substitution - Missense 16:3594566-3594566 - TCGA-39-5035-01 COSM703043 c.111C>A p.S37R Substitution - Missense 16:3608854-3608854 - 2492702 COSM5600528 c.976C>T p.L326L Substitution - coding silent 16:3601166-3601166 - SNU-175 COSM2919717 c.3116C>A p.P1039H Substitution - Missense 16:3590522-3590522 - CMPC11-3104 COSM2919688 c.3912C>T p.V1304V Substitution - coding silent 16:3589726-3589726 - TCGA-61-1915-01 COSM1324456 c.396A>G p.E132E Substitution - coding silent 16:3608569-3608569 - LUAD-B01811 COSM334032 c.1355G>C p.R452T Substitution - Missense 16:3597808-3597808 - TCGA-G9-6362-01 COSM1128966 c.3310C>T p.R1104W Substitution - Missense 16:3590328-3590328 - 220 COSM4425158 c.2966C>G p.S989* Substitution - Nonsense 16:3590672-3590672 - TCGA-EE-A2GR-06 COSM3509517 c.5090C>T p.P1697L Substitution - Missense 16:3583160-3583160 - CHC805T COSM4954349 c.1763A>G p.H588R Substitution - Missense 16:3596314-3596314 - 7T COSM3711925 c.3425C>T p.S1142L Substitution - Missense 16:3590213-3590213 - TCGA-AA-3821-01 COSM294837 c.398C>T p.P133L Substitution - Missense 16:3608567-3608567 - TCGA-H4-A2HQ-01 COSM1301952 c.2491G>T p.E831* Substitution - Nonsense 16:3591147-3591147 - Au2 COSM5600528 c.976C>T p.L326L Substitution - coding silent 16:3601166-3601166 - CSCC-31-T COSM4492829 c.4043C>T p.P1348L Substitution - Missense 16:3589595-3589595 - UM-SCC-2 COSM2919704 c.3367T>C p.S1123P Substitution - Missense 16:3590271-3590271 - TCGA-CD-A4MG-01 COSM4060667 c.561G>T p.Q187H Substitution - Missense 16:3606673-3606673 - TCGA-A3-3380-01 COSM471706 c.2460G>T p.R820S Substitution - Missense 16:3591178-3591178 - TCGA-BR-7707-01 COSM1185021 c.3850G>A p.V1284M Substitution - Missense 16:3589788-3589788 - TCGA-FW-A3R5-06 COSM3888510 c.5159C>T p.S1720F Substitution - Missense 16:3582688-3582688 - AOCS-124-1-X COSM2919671 c.4478C>T p.S1493L Substitution - Missense 16:3589160-3589160 - QC2-32-T2 COSM5654306 c.678C>T p.H226H Substitution - coding silent 16:3606556-3606556 - 1255_T COSM3957559 c.1749G>C p.R583S Substitution - Missense 16:3596328-3596328 - CSB12 COSM5028061 c.1307C>T p.A436V Substitution - Missense 16:3597856-3597856 - TCGA-A6-6780-01 COSM1377774 c.3667C>T p.P1223S Substitution - Missense 16:3589971-3589971 - AOCS-139-12-5 COSM3948538 c.2967A>T p.S989S Substitution - coding silent 16:3590671-3590671 - CSCC-31-T COSM4487055 c.3134C>T p.P1045L Substitution - Missense 16:3590504-3590504 - TCGA-22-5472-01 COSM703051 c.2813C>A p.A938E Substitution - Missense 16:3590825-3590825 - RKO COSM4647925 c.2192A>G p.D731G Substitution - Missense 16:3592834-3592834 - Sample_1 COSM5021855 c.610C>T p.R204C Substitution - Missense 16:3606624-3606624 - Pat_15_A COSM3509533 c.3118C>T p.P1040S Substitution - Missense 16:3590520-3590520 - TCGA-EE-A29V-06 COSM3509536 c.2551A>G p.M851V Substitution - Missense 16:3591087-3591087 - CRC-06T COSM5456541 c.4967C>A p.P1656H Substitution - Missense 16:3583283-3583283 - HCT-116 COSM1684428 c.4379_4389del11 p.A1461fs*2 Deletion - Frameshift 16:3589249-3589259 - HCC074T COSM5810319 c.1292A>T p.E431V Substitution - Missense 16:3597871-3597871 - B89-4-Tumor COSM1749595 c.3234G>C p.V1078V Substitution - coding silent 16:3590404-3590404 - TCGA-D1-A17F-01 COSM970476 c.5007G>A p.R1669R Substitution - coding silent 16:3583243-3583243 - TCGA-A6-6653-01 COSM1377771 c.3902G>A p.G1301E Substitution - Missense 16:3589736-3589736 - TCGA-EE-A3JD-06 COSM4396472 c.514C>T p.L172F Substitution - Missense 16:3608451-3608451 - TCGA-BS-A0UF-01 COSM970490 c.2454C>A p.L818L Substitution - coding silent 16:3591184-3591184 - RK048_C01 COSM1629890 c.795C>T p.D265D Substitution - coding silent 16:3602273-3602273 - SW1417 COSM2919711 c.3269C>T p.T1090M Substitution - Missense 16:3590369-3590369 - CHC1742T COSM4792210 c.2147T>G p.L716R Substitution - Missense 16:3594466-3594466 - ESCC_80 COSM5635759 c.1960G>A p.G654R Substitution - Missense 16:3595658-3595658 - SW48 COSM2919796 c.533G>T p.R178I Substitution - Missense 16:3608432-3608432 - sysucc-1135T COSM5479929 c.4226C>T p.A1409V Substitution - Missense 16:3589412-3589412 - LS411 COSM2919810 c.113T>C p.L38P Substitution - Missense 16:3608852-3608852 - TCGA-D1-A0ZO-01 COSM970505 c.503C>A p.P168Q Substitution - Missense 16:3608462-3608462 - sysucc-1171T COSM5452721 c.3024T>G p.S1008R Substitution - Missense 16:3590614-3590614 - 116T COSM1725447 c.3626G>C p.R1209T Substitution - Missense 16:3590012-3590012 - C086 COSM5539399 c.518C>T p.S173F Substitution - Missense 16:3608447-3608447 - TCGA-BR-4201-01 COSM1563124 c.5335C>T p.R1779W Substitution - Missense 16:3582512-3582512 - T3021 COSM4728194 c.1603G>A p.A535T Substitution - Missense 16:3597459-3597459 - BCB157T COSM4793532 c.4703T>C p.I1568T Substitution - Missense 16:3584805-3584805 - TCGA-G4-6310-01 COSM1377780 c.1673G>A p.R558Q Substitution - Missense 16:3597389-3597389 - Sample_1 COSM5021856 c.555C>T p.D185D Substitution - coding silent 16:3606679-3606679 - TCGA-ET-A2MZ-01 COSM3370429 c.2305G>C p.E769Q Substitution - Missense 16:3592721-3592721 - 2492724 COSM4465869 c.1403C>T p.P468L Substitution - Missense 16:3597659-3597659 - 50 COSM5734546 c.837delA p.G280fs*27 Deletion - Frameshift 16:3602231-3602231 - TCGA-D5-6928-01 COSM1377782 c.1250C>A p.P417Q Substitution - Missense 16:3597913-3597913 - 8036161 COSM3387430 c.3536A>C p.K1179T Substitution - Missense 16:3590102-3590102 - 2011-2374:2012-1302-T COSM294837 c.398C>T p.P133L Substitution - Missense 16:3608567-3608567 - TCGA-74-6575-01 COSM3402316 c.185T>C p.V62A Substitution - Missense 16:3608780-3608780 - TCGA-BS-A0UV-01 COSM970481 c.3676C>T p.R1226W Substitution - Missense 16:3589962-3589962 - BD148T COSM5521225 c.4304C>A p.P1435Q Substitution - Missense 16:3589334-3589334 - 31231321 COSM1582315 c.3089C>T p.P1030L Substitution - Missense 16:3590549-3590549 - TCGA-CM-6171-01 COSM1377778 c.1887C>T p.P629P Substitution - coding silent 16:3596190-3596190 - LUAD_E00565 COSM389169 c.5338G>A p.E1780K Substitution - Missense 16:3582509-3582509 - TCGA-AG-A002-01 COSM263760 c.2346C>T p.L782L Substitution - coding silent 16:3591292-3591292 - TCGA-CD-A4MJ-01 COSM1324457 c.709C>T p.R237W Substitution - Missense 16:3606525-3606525 - HCC113 COSM1609317 c.2843C>T p.A948V Substitution - Missense 16:3590795-3590795 - CCRF-CEM COSM1678804 c.2098G>A p.G700R Substitution - Missense 16:3594515-3594515 - T207 COSM81743 c.1242C>T p.D414D Substitution - coding silent 16:3597921-3597921 - TCGA-B7-5816-01 COSM4060645 c.5192C>T p.A1731V Substitution - Missense 16:3582655-3582655 - TCGA-AP-A051-01 COSM970497 c.1932C>T p.D644D Substitution - coding silent 16:3595686-3595686 - TCGA-CH-5739-01 COSM3672254 c.486G>T p.T162T Substitution - coding silent 16:3608479-3608479 - CSCC-44-T COSM2919671 c.4478C>T p.S1493L Substitution - Missense 16:3589160-3589160 - PT53 COSM5941395 c.4352C>T p.T1451I Substitution - Missense 16:3589286-3589286 - TCGA-ER-A1A1-06 COSM2919644 c.5336G>A p.R1779Q Substitution - Missense 16:3582511-3582511 - CCK81 COSM2919646 c.5249C>T p.A1750V Substitution - Missense 16:3582598-3582598 - T3720 COSM4728189 c.4339G>A p.G1447S Substitution - Missense 16:3589299-3589299 - TCGA-60-2722-01 COSM703046 c.611G>A p.R204H Substitution - Missense 16:3606623-3606623 - HCC107T COSM1609316 c.4584C>A p.A1528A Substitution - coding silent 16:3589054-3589054 - TCGA-EE-A2MD-06 COSM3509518 c.4994C>T p.P1665L Substitution - Missense 16:3583256-3583256 - TCGA-FW-A3R5-06 COSM3888511 c.5042C>T p.S1681L Substitution - Missense 16:3583208-3583208 - PCSI_0628_Pa_P_526 COSM5946246 c.3703C>G p.P1235A Substitution - Missense 16:3589935-3589935 - HN_62825 COSM127452 c.5238C>T p.A1746A Substitution - coding silent 16:3582609-3582609 - UM-SCC-2 COSM2919771 c.1378C>T p.R460C Substitution - Missense 16:3597684-3597684 - TCGA-DK-A1AC-01 COSM1301951 c.3428C>T p.S1143F Substitution - Missense 16:3590210-3590210 - TCGA-HF-7132-01 COSM4060658 c.2809G>T p.G937W Substitution - Missense 16:3590829-3590829 - CHC2048T COSM4793116 c.1156A>G p.M386V Substitution - Missense 16:3600986-3600986 - HCC155T COSM5823341 c.326A>G p.K109R Substitution - Missense 16:3608639-3608639 - 11M COSM5577070 c.449C>T p.P150L Substitution - Missense 16:3608516-3608516 - Patient_1_Relapse COSM5414972 c.3770T>G p.V1257G Substitution - Missense 16:3589868-3589868 - PTC-7C COSM4129049 c.3944C>T p.T1315I Substitution - Missense 16:3589694-3589694 - TCGA-D1-A15X-01 COSM970480 c.4034G>A p.R1345H Substitution - Missense 16:3589604-3589604 - TCGA-DD-A116-01 COSM4912264 c.990G>T p.V330V Substitution - coding silent 16:3601152-3601152 - CSCC-38-T COSM4470333 c.1654C>T p.P552S Substitution - Missense 16:3597408-3597408 - TCGA-D5-6532-01 COSM1377775 c.3662C>T p.A1221V Substitution - Missense 16:3589976-3589976 - HCC120 COSM3716919 c.4636+5G>A p.? Unknown 16:3588997-3588997 - TCGA-D3-A2JA-06 COSM3509516 c.5163C>T p.S1721S Substitution - coding silent 16:3582684-3582684 - TCGA-CG-5728-01 COSM4060668 c.430C>T p.L144F Substitution - Missense 16:3608535-3608535 - HCC034T COSM5817944 c.456G>T p.V152V Substitution - coding silent 16:3608509-3608509 - LAU50_2 COSM231863 c.3382C>A p.Q1128K Substitution - Missense 16:3590256-3590256 - TCGA-AP-A056-01 COSM703046 c.611G>A p.R204H Substitution - Missense 16:3606623-3606623 - CSCC-20-T COSM4516209 c.1695_1696GG>AA p.E566K Substitution - Missense 16:3596381-3596382 - CSCC-11-T COSM2919683 c.4031C>T p.S1344F Substitution - Missense 16:3589607-3589607 - Pat_15_B COSM5850883 c.4682C>T p.T1561M Substitution - Missense 16:3584826-3584826 - TCGA-21-1081-01 COSM703048 c.2518G>C p.E840Q Substitution - Missense 16:3591120-3591120 - YUCROFT COSM1708687 c.1976C>T p.S659L Substitution - Missense 16:3595642-3595642 - CHC1148T COSM4954571 c.3057T>C p.S1019S Substitution - coding silent 16:3590581-3590581 - ESCC_38 COSM5629075 c.5355G>C p.L1785L Substitution - coding silent 16:3582492-3582492 - TCGA-A6-6140-01 COSM3754892 c.2854G>A p.A952T Substitution - Missense 16:3590784-3590784 - TCGA-DA-A1IC-06 COSM3509524 c.4207G>A p.E1403K Substitution - Missense 16:3589431-3589431 - 2492703 COSM5600528 c.976C>T p.L326L Substitution - coding silent 16:3601166-3601166 - TCGA-D5-6537-01 COSM1377781 c.1630G>T p.D544Y Substitution - Missense 16:3597432-3597432 - TCGA-B0-4814-01 COSM3361759 c.835G>A p.V279I Substitution - Missense 16:3602233-3602233 - PT48 COSM5933487 c.3136C>T p.R1046C Substitution - Missense 16:3590502-3590502 - CHC1148T COSM4954571 c.3057T>C p.S1019S Substitution - coding silent 16:3590581-3590581 - LUAD-B02594 COSM336493 c.1245G>T p.E415D Substitution - Missense 16:3597918-3597918 - SC_9008 COSM5566326 c.1573C>T p.R525C Substitution - Missense 16:3597489-3597489 - TCGA-B5-A11E-01 COSM970492 c.2335G>A p.V779M Substitution - Missense 16:3591303-3591303 - YUWIA COSM5384867 c.498A>G p.Q166Q Substitution - coding silent 16:3608467-3608467 - TCGA-B5-A11E-01 COSM970496 c.1941C>T p.P647P Substitution - coding silent 16:3595677-3595677 - TCGA-G4-6588-01 COSM1377779 c.1745G>A p.R582Q Substitution - Missense 16:3596332-3596332 - TCGA-CG-4442-01 COSM4060660 c.2540A>G p.N847S Substitution - Missense 16:3591098-3591098 - CSCC-31-T COSM4496204 c.4701C>T p.S1567S Substitution - coding silent 16:3584807-3584807 - I2L-P11-Tumor-Organoid COSM2919716 c.3126C>T p.G1042G Substitution - coding silent 16:3590512-3590512 - TCGA-EU-5904-01 COSM471707 c.428T>A p.V143E Substitution - Missense 16:3608537-3608537 - TCGA-FW-A3R5-06 COSM970496 c.1941C>T p.P647P Substitution - coding silent 16:3595677-3595677 - OSCC-GB_01060111 COSM4882901 c.1001C>G p.P334R Substitution - Missense 16:3601141-3601141 - TCGA-13-0724-01 COSM81743 c.1242C>T p.D414D Substitution - coding silent 16:3597921-3597921 - Pat_15_B COSM3509533 c.3118C>T p.P1040S Substitution - Missense 16:3590520-3590520 - TCGA-CG-5734-01 COSM4060651 c.4249A>G p.S1417G Substitution - Missense 16:3589389-3589389 - Pat_46_A COSM5850884 c.4294C>T p.P1432S Substitution - Missense 16:3589344-3589344 - 3844_T COSM3957557 c.3383A>C p.Q1128P Substitution - Missense 16:3590255-3590255 - AOCS-141-8-0 COSM3948541 c.1222C>T p.R408W Substitution - Missense 16:3597941-3597941 - I2L-P26-Tumor-Organoid COSM5363581 c.2409G>C p.K803N Substitution - Missense 16:3591229-3591229 - TCGA-D3-A3MR-06 COSM3509521 c.4382C>T p.A1461V Substitution - Missense 16:3589256-3589256 - U2940 COSM5621863 c.2404G>A p.E802K Substitution - Missense 16:3591234-3591234 - TCGA-EE-A2MR-06 COSM3509519 c.4829C>T p.S1610F Substitution - Missense 16:3583421-3583421 - TCGA-EE-A2MR-06 COSM3509541 c.66C>T p.A22A Substitution - coding silent 16:3608899-3608899 - HCC024T COSM5823658 c.1574G>T p.R525L Substitution - Missense 16:3597488-3597488 - HCT116 COSM4612351 c.4381_4391del11 p.A1461fs*2 Deletion - Frameshift 16:3589247-3589257 - PD9000a COSM5775571 c.4688T>C p.M1563T Substitution - Missense 16:3584820-3584820 - BCB157T COSM4793532 c.4703T>C p.I1568T Substitution - Missense 16:3584805-3584805 - Sample_1 COSM5021854 c.1163+10C>T p.? Unknown 16:3600969-3600969 - PTC-7C COSM4129048 c.3945A>T p.T1315T Substitution - coding silent 16:3589693-3589693 - TCGA-B5-A11E-01 COSM970508 c.314G>T p.G105V Substitution - Missense 16:3608651-3608651 - T84 COSM2919662 c.4665C>T p.P1555P Substitution - coding silent 16:3584843-3584843 - TCGA-AA-3527-01 COSM291794 c.1335T>G p.S445R Substitution - Missense 16:3597828-3597828 - TCGA-BG-A0M8-01 COSM970483 c.3310C>A p.R1104R Substitution - coding silent 16:3590328-3590328 - NPC10F COSM4995658 c.92C>T p.S31F Substitution - Missense 16:3608873-3608873 - TCGA-AP-A051-01 COSM970507 c.384G>A p.W128* Substitution - Nonsense 16:3608581-3608581 - YURAY COSM5384866 c.516T>A p.L172L Substitution - coding silent 16:3608449-3608449 - TCGA-BR-8367-01 COSM4060649 c.4483G>A p.A1495T Substitution - Missense 16:3589155-3589155 - OSCC-GB_00880111 COSM4887973 c.322G>T p.E108* Substitution - Nonsense 16:3608643-3608643 - YUKLAB COSM1609317 c.2843C>T p.A948V Substitution - Missense 16:3590795-3590795 - HCC2998 COSM2919645 c.5252A>G p.D1751G Substitution - Missense 16:3582595-3582595 - CSCC-6-T COSM4492790 c.4038C>T p.P1346P Substitution - coding silent 16:3589600-3589600 - TCGA-FS-A1ZZ-06 COSM3509523 c.4237C>T p.P1413S Substitution - Missense 16:3589401-3589401 - NCI-H23 COSM1684429 c.3439_3441delGAA p.E1148delE Deletion - In frame 16:3590197-3590199 - T1154 COSM970482 c.3401C>T p.S1134L Substitution - Missense 16:3590237-3590237 - CSCC-29-T COSM4478620 c.2253C>T p.F751F Substitution - coding silent 16:3592773-3592773 - LUAD-RT-S01769 COSM380898 c.2848G>A p.E950K Substitution - Missense 16:3590790-3590790 - TCGA-AR-A0U3-01 COSM435233 c.3445G>T p.D1149Y Substitution - Missense 16:3590193-3590193 - YUKAT COSM5384865 c.789G>A p.E263E Substitution - coding silent 16:3602279-3602279 - TCGA-B8-4621-01 COSM471703 c.4439G>A p.G1480E Substitution - Missense 16:3589199-3589199 - HCC113T COSM1609317 c.2843C>T p.A948V Substitution - Missense 16:3590795-3590795 - PT46 COSM1377772 c.3812C>T p.S1271F Substitution - Missense 16:3589826-3589826 - TCGA-AX-A0J1-01 COSM970488 c.2617G>A p.A873T Substitution - Missense 16:3591021-3591021 - TCGA-B5-A0JV-01 COSM970485 c.3166delC p.L1056fs*60 Deletion - Frameshift 16:3590472-3590472 - CSCC-41-T COSM4543914 c.3465G>A p.L1155L Substitution - coding silent 16:3590173-3590173 - TCGA-18-3409-01 COSM703044 c.362A>G p.K121R Substitution - Missense 16:3608603-3608603 - TCGA-BR-A4PD-01 COSM4060652 c.3472G>A p.D1158N Substitution - Missense 16:3590166-3590166 - TCGA-AP-A0LM-01 COSM970486 c.3062G>A p.R1021H Substitution - Missense 16:3590576-3590576 - 587224 COSM1185022 c.4097G>A p.R1366H Substitution - Missense 16:3589541-3589541 - CSCC-20-T COSM4494035 c.4255C>T p.P1419S Substitution - Missense 16:3589383-3589383 - TCGA-FS-A1ZZ-06 COSM3509540 c.826T>C p.F276L Substitution - Missense 16:3602242-3602242 - 61 COSM5740543 c.1232G>A p.R411Q Substitution - Missense 16:3597931-3597931 - TCGA-D1-A0ZQ-01 COSM970477 c.4750C>T p.R1584C Substitution - Missense 16:3583500-3583500 - 721LT COSM294837 c.398C>T p.P133L Substitution - Missense 16:3608567-3608567 - TCGA-G4-6586-01 COSM1377766 c.5208C>T p.G1736G Substitution - coding silent 16:3582639-3582639 - TCGA-36-1578-01 COSM82032 c.723C>G p.V241V Substitution - coding silent 16:3606511-3606511 - CSCC-27-T COSM4549813 c.4834G>A p.D1612N Substitution - Missense 16:3583416-3583416 - TCGA-E2-A10C-01 COSM435232 c.4881G>C p.Q1627H Substitution - Missense 16:3583369-3583369 - TCGA-CG-5734-01 COSM4060654 c.3190G>A p.G1064R Substitution - Missense 16:3590448-3590448 - HCT8 COSM4634082 c.1352T>C p.I451T Substitution - Missense 16:3597811-3597811 - AOCS-135-3-1 COSM3948539 c.2259C>G p.H753Q Substitution - Missense 16:3592767-3592767 - 8032817 COSM3387432 c.1319C>T p.A440V Substitution - Missense 16:3597844-3597844 - CSCC-27-T COSM4473179 c.1833C>T p.A611A Substitution - coding silent 16:3596244-3596244 - TCGA-CM-5861-01 COSM1377768 c.4596C>T p.S1532S Substitution - coding silent 16:3589042-3589042 - TCGA-CG-5728-01 COSM4060656 c.3090G>A p.P1030P Substitution - coding silent 16:3590548-3590548 - TCGA-A6-6780-01 COSM1377787 c.921C>T p.N307N Substitution - coding silent 16:3602147-3602147 - DLD1 COSM4623333 c.2955G>T p.Q985H Substitution - Missense 16:3590683-3590683 - TCGA-33-4547-01 COSM703047 c.810G>C p.L270F Substitution - Missense 16:3602258-3602258 - HN_62897 COSM127083 c.4636+1G>C p.? Unknown 16:3589001-3589001 - Capan-1 COSM328363 c.3178C>T p.R1060W Substitution - Missense 16:3590460-3590460 - 587376 COSM1185027 c.2562T>G p.I854M Substitution - Missense 16:3591076-3591076 - PT34 COSM5910894 c.951-6C>T p.? Unknown 16:3601197-3601197 - sysucc-1317T COSM970484 c.3184C>T p.R1062C Substitution - Missense 16:3590454-3590454 - TCGA-F4-6809-01 COSM1377773 c.3721C>T p.R1241C Substitution - Missense 16:3589917-3589917 - ccRCC-77 COSM1664263 c.3583A>G p.I1195V Substitution - Missense 16:3590055-3590055 - S0078 COSM5882712 c.1640C>T p.T547M Substitution - Missense 16:3597422-3597422 - TCGA-61-2610-02 COSM1324459 c.2912A>G p.E971G Substitution - Missense 16:3590726-3590726 - TCGA-AP-A0LM-01 COSM970478 c.4577C>A p.P1526H Substitution - Missense 16:3589061-3589061 - T3021 COSM4728193 c.2137C>A p.R713R Substitution - coding silent 16:3594476-3594476 - I2L-P11-Tumor-Biopsy COSM2919716 c.3126C>T p.G1042G Substitution - coding silent 16:3590512-3590512 - 61 COSM5740542 c.4741T>G p.F1581V Substitution - Missense 16:3583509-3583509 - TCGA-BR-8487-01 COSM4060663 c.1353A>G p.I451M Substitution - Missense 16:3597810-3597810 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.143681 16p13.3 613278 235608|dbSNP|BC036335|A/G|non-coding||3908|Validated; 1200814|dbSNP|BC036335|C/T|non-coding||3896|Validated

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C IntronicSNV . c.951-101T>G 16 3651293 ESCA A C Missense p.S445R c.1335T>G 16 3647829 COREAD A C Synonymous p.P245P c.735T>G 16 3656500 STAD A C Synonymous p.V678V c.2034T>G 16 3644580 CM A G Missense p.F276L c.826T>C 16 3652243 CM A G Missense p.V62A c.185T>C 16 3658781 GBM A G Synonymous p.C1467C c.4401T>C 16 3639238 HC A T Missense p.S476T c.1426T>A 16 3647637 COREAD A T Missense p.V143E c.428T>A 16 3658538 RCCC A T Synonymous p.R486R c.1458T>A 16 3647605 COREAD C A Missense p.A1221S c.3661G>T 16 3639978 BLCA C A Missense p.D1149Y c.3445G>T 16 3640194 BRCA C A Missense p.E796D c.2388G>T 16 3641251 UCEC C A Missense p.G141W c.421G>T 16 3658545 LUAD C A Missense p.L224F c.672G>T 16 3656563 BRCA C A Missense p.Q991H c.2973G>T 16 3640666 LUAD C A Missense p.R1187M c.3560G>T 16 3640079 HNSC C A Missense p.R820S c.2460G>T 16 3641179 RCCC C A Missense p.W1428C c.4284G>T 16 3639355 OV C A Nonsense p.E831* c.2491G>T 16 3641148 BLCA C A Synonymous p.S1157S c.3471G>T 16 3640168 CM C G Missense p.E1701Q c.5101G>C 16 3633150 LUSC C G Missense p.E444Q c.1330G>C 16 3647834 COREAD C G Missense p.E456D c.1368G>C 16 3647695 BRCA C G Missense p.E840Q c.2518G>C 16 3641121 LUSC C G Missense p.E841Q c.2521G>C 16 3641118 LUSC C G Missense p.L193F c.579G>C 16 3656656 HNSC C G Missense p.L270F c.810G>C 16 3652259 LUSC C G SpliceDonorSNV . c.4636+1G>C 16 3639002 HNSC C T Missense p.A227T c.679G>A 16 3656556 UCEC C T Missense p.A758T c.2272G>A 16 3642755 MM C T Missense p.E1403K c.4207G>A 16 3639432 CM C T Missense p.E1780K c.5338G>A 16 3632510 HNSC C T Missense p.E230K c.688G>A 16 3656547 BLCA C T Missense p.E496K c.1486G>A 16 3647577 COREAD C T Missense p.E828K c.2482G>A 16 3641157 CM C T Missense p.E848K c.2542G>A 16 3641097 BRCA C T Missense p.G1480E c.4439G>A 16 3639200 RCCC C T Missense p.G648S c.1942G>A 16 3645677 MM C T Missense p.R1779Q c.5336G>A 16 3632512 CM C T Missense p.R204H c.611G>A 16 3656624 LUSC C T Missense p.V279I c.835G>A 16 3652234 RCCC C T Missense p.V308M c.922G>A 16 3652147 UCEC C T Nonsense p.W823* c.2469G>A 16 3641170 RCCC C T Synonymous p.A236A c.708G>A 16 3656527 HNSC C T Synonymous p.A440A c.1320G>A 16 3647844 UCEC C T Synonymous p.A948A c.2844G>A 16 3640795 UCEC C T Synonymous p.P1030P c.3090G>A 16 3640549 STAD C T Synonymous p.P600P c.1800G>A 16 3646278 HNSC C T Synonymous p.P715P c.2145G>A 16 3644469 UCEC C T Synonymous p.Q1041Q c.3123G>A 16 3640516 STAD C T Synonymous p.Q1485Q c.4455G>A 16 3639184 HNSC C T Synonymous p.R1669R c.5007G>A 16 3633244 UCEC C T Synonymous p.S1508S c.4524G>A 16 3639115 STAD G A Missense p.A1461V c.4382C>T 16 3639257 CM G A Missense p.A157V c.470C>T 16 3658496 PRAD G A Missense p.A1623V c.4868C>T 16 3633383 STAD G A Missense p.A1731V c.5192C>T 16 3632656 STAD G A Missense p.A436V c.1307C>T 16 3647857 BRCA G A Missense p.A505V c.1514C>T 16 3647549 UCEC G A Missense p.L144F c.430C>T 16 3658536 STAD G A Missense p.L172F c.514C>T 16 3658452 CM G A Missense p.P1040S c.3118C>T 16 3640521 CM G A Missense p.P1175S c.3523C>T 16 3640116 CM G A Missense p.P1261S c.3781C>T 16 3639858 CM G A Missense p.P1321S c.3961C>T 16 3639678 CM G A Missense p.P1343L c.4028C>T 16 3639611 CM G A Missense p.P1346L c.4037C>T 16 3639602 CM G A Missense p.P1413S c.4237C>T 16 3639402 CM G A Missense p.P1619L c.4856C>T 16 3633395 CM G A Missense p.P1665L c.4994C>T 16 3633257 CM G A Missense p.P1697L c.5090C>T 16 3633161 CM G A Missense p.R1060W c.3178C>T 16 3640461 CM G A Missense p.R1104W c.3310C>T 16 3640329 PRAD G A Missense p.R1584C c.4750C>T 16 3633501 UCEC G A Missense p.R1779W c.5335C>T 16 3632513 STAD G A Missense p.R398W c.1192C>T 16 3647972 STAD G A Missense p.S1406F c.4217C>T 16 3639422 CM G A Missense p.S1492F c.4475C>T 16 3639164 CM G A Missense p.S659L c.1976C>T 16 3645643 HNSC G A Missense p.S973F c.2918C>T 16 3640721 CM G A Nonsense p.Q1408* c.4222C>T 16 3639417 HNSC G A Nonsense p.Q1632* c.4894C>T 16 3633357 SCLC G A Synonymous p.A1746A c.5238C>T 16 3632610 HNSC G A Synonymous p.D265D c.795C>T 16 3652274 HC G A Synonymous p.D414D c.1242C>T 16 3647922 OV G A Synonymous p.D731D c.2193C>T 16 3642834 ESCA G A Synonymous p.D731D c.2193C>T 16 3642834 GBM G A Synonymous p.D876D c.2628C>T 16 3641011 STAD G A Synonymous p.F59F c.177C>T 16 3658789 CM G A Synonymous p.L1586L c.4756C>T 16 3633495 CM G A Synonymous p.L366L c.1098C>T 16 3651045 NB G A Synonymous p.L818L c.2454C>T 16 3641185 CM G A Synonymous p.L986L c.2958C>T 16 3640681 PRAD G A Synonymous p.S1721S c.5163C>T 16 3632685 CM G A Synonymous p.Y983Y c.2949C>T 16 3640690 LGG G C Missense p.P342R c.1025C>G 16 3651118 HNSC G C Missense p.S173C c.518C>G 16 3658448 LUSC G C Missense p.T1809S c.5426C>G 16 3632422 BRCA G C Synonymous p.P1327P c.3981C>G 16 3639658 CM G C Synonymous p.V241V c.723C>G 16 3656512 OV G - Frameshift p.L1056Cfs*60 c.3166delC 16 3640473 UCEC G - Frameshift p.V1558Cfs*3 c.4668delC 16 3634841 LUAD GG AA Missense p.P1059L c.3176_3177delinsTT 16 3640462 CM GG AA Missense p.P944F c.2830_2831delinsTT 16 3640808 CM G T Missense p.A938E c.2813C>A 16 3640826 LUSC G T Missense p.P885Q c.2654C>A 16 3640985 CM G T Missense p.S37R c.111C>A 16 3658855 LUSC G T Nonsense p.Y1601* c.4803C>A 16 3633448 LUSC G T Synonymous p.I994I c.2982C>A 16 3640657 RCCC G T Synonymous p.S1497S c.4491C>A 16 3639148 LUAD T C Missense p.K78R c.233A>G 16 3658733 CM T C Missense p.M851V c.2551A>G 16 3641088 CM T C Missense p.S1417G c.4249A>G 16 3639390 STAD T C Synonymous p.P502P c.1506A>G 16 3647557 LUAD