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 23 40982957 40982957 + Frame_Shift_Del DEL C C - TCGA-OR-A5J5-01A-11D-A29I-10 TCGA-OR-A5J5-10A-01D-A29L-10 g.chrX:40982957delC c.76delC c.(76-78)cccfs p.P27fs ACC 23 41025466 41025466 + Splice_Site SNP G G C TCGA-OR-A5KB-01A-11D-A30A-10 TCGA-OR-A5KB-11A-11D-A30A-10 g.chrX:41025466G>C c.2327G>C c.(2326-2328)aGg>aCg p.R776T ACC 23 41075161 41075161 + Missense_Mutation SNP G G A TCGA-OR-A5LJ-01A-11D-A29I-10 TCGA-OR-A5LJ-10A-01D-A29L-10 g.chrX:41075161G>A c.5341G>A c.(5341-5343)Gta>Ata p.V1781I BLCA 23 41007694 41007694 + Missense_Mutation SNP G G A TCGA-FD-A3SS-01A-12D-A22Z-08 TCGA-FD-A3SS-10A-01D-A22Z-08 g.chrX:41007694G>A c.1492G>A c.(1492-1494)Gat>Aat p.D498N BLCA 23 41010204 41010204 + Missense_Mutation SNP G G C TCGA-DK-A3X1-01A-12D-A22Z-08 TCGA-DK-A3X1-10A-01D-A22Z-08 g.chrX:41010204G>C c.1657G>C c.(1657-1659)Gat>Cat p.D553H BLCA 23 41025165 41025165 + Missense_Mutation SNP C C G TCGA-DK-A6B6-01A-11D-A30E-08 TCGA-DK-A6B6-10A-01D-A30H-08 g.chrX:41025165C>G c.2026C>G c.(2026-2028)Cag>Gag p.Q676E BLCA 23 41027283 41027283 + Missense_Mutation SNP T T G TCGA-UY-A9PB-01A-11D-A38G-08 TCGA-UY-A9PB-10A-01D-A38J-08 g.chrX:41027283T>G c.2448T>G c.(2446-2448)atT>atG p.I816M BLCA 23 41027293 41027293 + Missense_Mutation SNP T T G TCGA-UY-A9PB-01A-11D-A38G-08 TCGA-UY-A9PB-10A-01D-A38J-08 g.chrX:41027293T>G c.2458T>G c.(2458-2460)Ttt>Gtt p.F820V BLCA 23 41027317 41027317 + Missense_Mutation SNP G G A TCGA-4Z-AA7R-01A-11D-A391-08 TCGA-4Z-AA7R-10A-01D-A394-08 g.chrX:41027317G>A c.2482G>A c.(2482-2484)Gac>Aac p.D828N BLCA 23 41029374 41029374 + Silent SNP T T C TCGA-XF-A9T6-01A-11D-A42E-08 TCGA-XF-A9T6-10A-01D-A42H-08 g.chrX:41029374T>C c.2763T>C c.(2761-2763)aaT>aaC p.N921N BLCA 23 41029731 41029731 + Silent SNP A A T TCGA-UY-A9PE-01A-11D-A38G-08 TCGA-UY-A9PE-10A-01D-A38J-08 g.chrX:41029731A>T c.2886A>T c.(2884-2886)acA>acT p.T962T BLCA 23 41047252 41047252 + Missense_Mutation SNP G G C TCGA-4Z-AA86-01A-11D-A391-08 TCGA-4Z-AA86-10A-01D-A394-08 g.chrX:41047252G>C c.3692G>C c.(3691-3693)aGa>aCa p.R1231T BLCA 23 41047370 41047371 + Splice_Site INS - - GT TCGA-BT-A2LB-01A-11D-A18F-08 TCGA-BT-A2LB-10A-01D-A18F-08 g.chrX:41047370_41047371insGT c.3810_3810insGT c.(3811-3813)acc>acGTc p.T1271fs BLCA 23 41056737 41056737 + Missense_Mutation SNP G G A TCGA-ZF-AA54-01A-11D-A391-08 TCGA-ZF-AA54-10A-01D-A394-08 g.chrX:41056737G>A c.4354G>A c.(4354-4356)Gaa>Aaa p.E1452K BLCA 23 41057842 41057842 + Missense_Mutation SNP G G A TCGA-GC-A6I1-01A-12D-A31L-08 TCGA-GC-A6I1-10A-01D-A31J-08 g.chrX:41057842G>A c.4442G>A c.(4441-4443)gGa>gAa p.G1481E BLCA 23 41060386 41060386 + Silent SNP G G C TCGA-XF-AAMZ-01A-11D-A42E-08 TCGA-XF-AAMZ-10A-01D-A42H-08 g.chrX:41060386G>C c.4677G>C c.(4675-4677)ctG>ctC p.L1559L BLCA 23 41060455 41060455 + Missense_Mutation SNP G G C TCGA-XF-A9SY-01A-21D-A42E-08 TCGA-XF-A9SY-10A-01D-A42H-08 g.chrX:41060455G>C c.4746G>C c.(4744-4746)agG>agC p.R1582S BLCA 23 41075732 41075732 + Missense_Mutation SNP A A G TCGA-BT-A3PK-01A-21D-A21Z-08 TCGA-BT-A3PK-10A-01D-A21Z-08 g.chrX:41075732A>G c.5912A>G c.(5911-5913)gAg>gGg p.E1971G BLCA 23 41077663 41077663 + Missense_Mutation SNP A A T TCGA-BT-A0YX-01A-11D-A10S-08 TCGA-BT-A0YX-10A-01D-A10S-08 g.chrX:41077663A>T c.6248A>T c.(6247-6249)aAt>aTt p.N2083I BLCA 23 41084104 41084104 + Missense_Mutation SNP G G C TCGA-ZF-A9R7-01A-11D-A38G-08 TCGA-ZF-A9R7-10A-01D-A38J-08 g.chrX:41084104G>C c.6861G>C c.(6859-6861)aaG>aaC p.K2287N BLCA 23 41088555 41088555 + Missense_Mutation SNP G G C TCGA-UY-A9PB-01A-11D-A38G-08 TCGA-UY-A9PB-10A-01D-A38J-08 g.chrX:41088555G>C c.7111G>C c.(7111-7113)Gac>Cac p.D2371H BRCA 23 40990740 40990741 + Frame_Shift_Del DEL AG AG - TCGA-A2-A1FV-01A-11D-A13L-09 TCGA-A2-A1FV-10A-01D-A13O-09 g.chrX:40990740_40990741delAG c.273_274delAG c.(271-276)aaagggfs p.G92fs BRCA 23 40990750 40990750 + Missense_Mutation SNP G G C TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chrX:40990750G>C c.283G>C c.(283-285)Gaa>Caa p.E95Q BRCA 23 41007789 41007789 + Silent SNP C C T TCGA-AR-A2LE-01A-11D-A17W-09 TCGA-AR-A2LE-10A-01D-A17W-09 g.chrX:41007789C>T c.1587C>T c.(1585-1587)ctC>ctT p.L529L BRCA 23 41010191 41010191 + Missense_Mutation SNP G G T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chrX:41010191G>T c.1644G>T c.(1642-1644)aaG>aaT p.K548N BRCA 23 41012240 41012240 + Silent SNP C C T TCGA-D8-A1XZ-01A-11D-A14K-09 TCGA-D8-A1XZ-10A-01D-A14K-09 g.chrX:41012240C>T c.1803C>T c.(1801-1803)gaC>gaT p.D601D BRCA 23 41025364 41025364 + Missense_Mutation SNP G G A TCGA-B6-A0X7-01A-11D-A10M-09 TCGA-B6-A0X7-10A-01D-A10M-09 g.chrX:41025364G>A c.2225G>A c.(2224-2226)cGa>cAa p.R742Q BRCA 23 41025387 41025387 + Nonsense_Mutation SNP C C T TCGA-D8-A1X7-01A-11D-A14K-09 TCGA-D8-A1X7-10A-01D-A14K-09 g.chrX:41025387C>T c.2248C>T c.(2248-2250)Cga>Tga p.R750* BRCA 23 41043849 41043849 + Missense_Mutation SNP C C G TCGA-E9-A1RF-01A-11D-A159-09 TCGA-E9-A1RF-10A-01D-A159-09 g.chrX:41043849C>G c.3479C>G c.(3478-3480)aCt>aGt p.T1160S BRCA 23 41047365 41047365 + Missense_Mutation SNP G G C TCGA-C8-A26Y-01A-11D-A16D-09 TCGA-C8-A26Y-10A-01D-A16D-09 g.chrX:41047365G>C c.3805G>C c.(3805-3807)Gag>Cag p.E1269Q BRCA 23 41048627 41048627 + Missense_Mutation SNP G G A TCGA-BH-A18U-01A-21D-A12B-09 TCGA-BH-A18U-11A-23D-A12B-09 g.chrX:41048627G>A c.3876G>A c.(3874-3876)atG>atA p.M1292I BRCA 23 41048632 41048633 + Frame_Shift_Ins INS - - A TCGA-AN-A0XN-01A-21D-A10G-09 TCGA-AN-A0XN-10A-01D-A10G-09 g.chrX:41048632_41048633insA c.3881_3882insA c.(3880-3885)ttatgtfs p.C1295fs BRCA 23 41048645 41048645 + Missense_Mutation SNP G G C TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chrX:41048645G>C c.3894G>C c.(3892-3894)ttG>ttC p.L1298F BRCA 23 41055854 41055855 + Frame_Shift_Del DEL AG AG - TCGA-BH-A18G-01A-11D-A12B-09 TCGA-BH-A18G-10A-01D-A12B-09 g.chrX:41055854_41055855delAG c.4096_4097delAG c.(4096-4098)agafs p.R1366fs BRCA 23 41056704 41056704 + Nonsense_Mutation SNP C C T TCGA-EW-A1J5-01A-11D-A13L-09 TCGA-EW-A1J5-10A-01D-A13O-09 g.chrX:41056704C>T c.4321C>T c.(4321-4323)Caa>Taa p.Q1441* BRCA 23 41073963 41073963 + Splice_Site SNP G G A TCGA-AC-A2FM-01A-11D-A19Y-09 TCGA-AC-A2FM-11B-32D-A19Y-09 g.chrX:41073963G>A c.e34+1 BRCA 23 41075185 41075185 + Silent SNP T T C TCGA-A2-A0T3-01A-21D-A10Y-09 TCGA-A2-A0T3-10A-01D-A110-09 g.chrX:41075185T>C c.5365T>C c.(5365-5367)Tta>Cta p.L1789L BRCA 23 41075313 41075313 + Silent SNP T T G TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chrX:41075313T>G c.5493T>G c.(5491-5493)ggT>ggG p.G1831G BRCA 23 41075620 41075620 + Missense_Mutation SNP A A C TCGA-GM-A2DB-01A-31D-A19Y-09 TCGA-GM-A2DB-10C-01D-A18P-09 g.chrX:41075620A>C c.5800A>C c.(5800-5802)Atg>Ctg p.M1934L BRCA 23 41075653 41075653 + Missense_Mutation SNP T T G TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chrX:41075653T>G c.5833T>G c.(5833-5835)Tgg>Ggg p.W1945G BRCA 23 41076559 41076559 + Missense_Mutation SNP C C G TCGA-AN-A0G0-01A-11W-A050-09 TCGA-AN-A0G0-10A-01W-A055-09 g.chrX:41076559C>G c.6172C>G c.(6172-6174)Cac>Gac p.H2058D BRCA 23 41082490 41082490 + Missense_Mutation SNP C C G TCGA-A7-A26J-01A-11D-A167-09 TCGA-A7-A26J-10A-01D-A167-09 g.chrX:41082490C>G c.6586C>G c.(6586-6588)Ctt>Gtt p.L2196V BRCA 23 41084197 41084198 + Frame_Shift_Ins INS - - A TCGA-AO-A12H-01A-11D-A10Y-09 TCGA-AO-A12H-10A-01D-A110-09 g.chrX:41084197_41084198insA c.6954_6955insA c.(6955-6957)agtfs p.S2319fs CESC 23 40999952 40999952 + Missense_Mutation SNP G G A TCGA-EA-A3HU-01A-11D-A20U-09 TCGA-EA-A3HU-10B-01D-A20U-09 g.chrX:40999952G>A c.698G>A c.(697-699)gGg>gAg p.G233E CESC 23 41029361 41029361 + Missense_Mutation SNP G G A TCGA-C5-A3HE-01A-21D-A22X-09 TCGA-C5-A3HE-10A-01D-A22X-09 g.chrX:41029361G>A c.2750G>A c.(2749-2751)cGa>cAa p.R917Q CESC 23 41043695 41043695 + Missense_Mutation SNP G G A TCGA-JW-A852-01A-11D-A351-09 TCGA-JW-A852-10A-01D-A351-09 g.chrX:41043695G>A c.3325G>A c.(3325-3327)Gat>Aat p.D1109N CESC 23 41047349 41047350 + Frame_Shift_Ins INS - - TT TCGA-EK-A2PM-01A-11D-A18J-09 TCGA-EK-A2PM-10A-01D-A18J-09 g.chrX:41047349_41047350insTT c.3789_3790insTT c.(3790-3792)atcfs p.I1264fs CESC 23 41055534 41055534 + Missense_Mutation SNP C C A TCGA-FU-A3HZ-01A-11D-A20U-09 TCGA-FU-A3HZ-10A-01D-A20U-09 g.chrX:41055534C>A c.4008C>A c.(4006-4008)ttC>ttA p.F1336L CESC 23 41055965 41055965 + Missense_Mutation SNP G G A TCGA-C5-A3HD-01B-11D-A20U-09 TCGA-C5-A3HD-10A-01D-A20U-09 g.chrX:41055965G>A c.4207G>A c.(4207-4209)Gaa>Aaa p.E1403K CESC 23 41075524 41075524 + Missense_Mutation SNP G G A TCGA-EA-A439-01A-11D-A243-09 TCGA-EA-A439-10A-01D-A243-09 g.chrX:41075524G>A c.5704G>A c.(5704-5706)Gat>Aat p.D1902N CESC 23 41077746 41077746 + Missense_Mutation SNP G G A TCGA-C5-A1BM-01A-11D-A13W-08 TCGA-C5-A1BM-10A-01D-A13W-08 g.chrX:41077746G>A c.6331G>A c.(6331-6333)Gaa>Aaa p.E2111K CESC 23 41089034 41089035 + Frame_Shift_Ins INS - - A TCGA-EA-A3HU-01A-11D-A20U-09 TCGA-EA-A3HU-10B-01D-A20U-09 g.chrX:41089034_41089035insA c.7433_7434insA c.(7432-7437)gtaaaafs p.VK2478fs CHOL 23 41043819 41043819 + Missense_Mutation SNP A A G TCGA-W5-AA33-01A-11D-A417-09 TCGA-W5-AA33-10A-01D-A41A-09 g.chrX:41043819A>G c.3449A>G c.(3448-3450)aAt>aGt p.N1150S CHOL 23 41088540 41088540 + Nonsense_Mutation SNP C C T TCGA-ZU-A8S4-01A-11D-A417-09 TCGA-ZU-A8S4-10A-01D-A41A-09 g.chrX:41088540C>T c.7096C>T c.(7096-7098)Cga>Tga p.R2366* COAD 23 40982912 40982912 + Missense_Mutation SNP G G A TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chrX:40982912G>A c.31G>A c.(31-33)Gga>Aga p.G11R COAD 23 40988350 40988350 + Missense_Mutation SNP C C A TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chrX:40988350C>A c.194C>A c.(193-195)cCt>cAt p.P65H COAD 23 40988387 40988387 + Silent SNP C C T TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chrX:40988387C>T c.231C>T c.(229-231)gaC>gaT p.D77D COAD 23 40990744 40990744 + Nonsense_Mutation SNP G G T TCGA-A6-5660-01A-01D-1650-10 TCGA-A6-5660-10A-01D-1650-10 g.chrX:40990744G>T c.277G>T c.(277-279)Gaa>Taa p.E93* COAD 23 40996081 40996081 + Missense_Mutation SNP C C T TCGA-CM-6680-01A-11D-1835-10 TCGA-CM-6680-10A-01D-1835-10 g.chrX:40996081C>T c.460C>T c.(460-462)Cgt>Tgt p.R154C COAD 23 41000437 41000437 + Missense_Mutation SNP A A C TCGA-CK-4950-01A-01D-1719-10 TCGA-CK-4950-10A-01D-1719-10 g.chrX:41000437A>C c.989A>C c.(988-990)aAc>aCc p.N330T COAD 23 41010222 41010222 + Missense_Mutation SNP C C A TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chrX:41010222C>A c.1675C>A c.(1675-1677)Ctt>Att p.L559I COAD 23 41022042 41022042 + Splice_Site SNP G G A TCGA-CM-6165-01A-11D-1650-10 TCGA-CM-6165-10A-01D-1650-10 g.chrX:41022042G>A c.e15-1 COAD 23 41025167 41025167 + Missense_Mutation SNP G G T TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chrX:41025167G>T c.2028G>T c.(2026-2028)caG>caT p.Q676H COAD 23 41025219 41025219 + Missense_Mutation SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chrX:41025219C>T c.2080C>T c.(2080-2082)Cgt>Tgt p.R694C COAD 23 41025392 41025392 + Missense_Mutation SNP A A C TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chrX:41025392A>C c.2253A>C c.(2251-2253)gaA>gaC p.E751D COAD 23 41027380 41027380 + Nonsense_Mutation SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chrX:41027380C>T c.2545C>T c.(2545-2547)Cga>Tga p.R849* COAD 23 41029361 41029361 + Missense_Mutation SNP G G A TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chrX:41029361G>A c.2750G>A c.(2749-2751)cGa>cAa p.R917Q COAD 23 41045782 41045782 + Missense_Mutation SNP A A G TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chrX:41045782A>G c.3571A>G c.(3571-3573)Acc>Gcc p.T1191A COAD 23 41045841 41045841 + Silent SNP C C T TCGA-AA-3518-01A-02W-0833-10 TCGA-AA-3518-10A-01W-0833-10 g.chrX:41045841C>T c.3630C>T c.(3628-3630)tcC>tcT p.S1210S COAD 23 41047291 41047291 + Missense_Mutation SNP A A C TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chrX:41047291A>C c.3731A>C c.(3730-3732)aAa>aCa p.K1244T COAD 23 41055599 41055599 + Missense_Mutation SNP T T C TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chrX:41055599T>C c.4073T>C c.(4072-4074)tTt>tCt p.F1358S COAD 23 41055978 41055978 + Missense_Mutation SNP T T G TCGA-CM-5864-01A-01D-1650-10 TCGA-CM-5864-10A-01D-1650-10 g.chrX:41055978T>G c.4220T>G c.(4219-4221)cTt>cGt p.L1407R COAD 23 41057839 41057839 + Missense_Mutation SNP A A C TCGA-CM-5864-01A-01D-1650-10 TCGA-CM-5864-10A-01D-1650-10 g.chrX:41057839A>C c.4439A>C c.(4438-4440)aAt>aCt p.N1480T COAD 23 41064704 41064704 + Missense_Mutation SNP G G A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chrX:41064704G>A c.4973G>A c.(4972-4974)cGa>cAa p.R1658Q COAD 23 41069809 41069809 + Missense_Mutation SNP A A C TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chrX:41069809A>C c.5063A>C c.(5062-5064)gAa>gCa p.E1688A COAD 23 41073882 41073882 + Missense_Mutation SNP C C A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chrX:41073882C>A c.5251C>A c.(5251-5253)Ctt>Att p.L1751I COAD 23 41073946 41073946 + Frame_Shift_Del DEL A A - TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chrX:41073946delA c.5315delA c.(5314-5316)gaafs p.E1772fs COAD 23 41075428 41075428 + Missense_Mutation SNP G G A TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chrX:41075428G>A c.5608G>A c.(5608-5610)Gta>Ata p.V1870I COAD 23 41075439 41075439 + Silent SNP T T G TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chrX:41075439T>G c.5619T>G c.(5617-5619)ggT>ggG p.G1873G COAD 23 41075506 41075506 + Missense_Mutation SNP C C T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chrX:41075506C>T c.5686C>T c.(5686-5688)Cgc>Tgc p.R1896C COAD 23 41075555 41075555 + Missense_Mutation SNP A A G TCGA-D5-6537-01A-11D-1719-10 TCGA-D5-6537-10A-01D-1719-10 g.chrX:41075555A>G c.5735A>G c.(5734-5736)gAt>gGt p.D1912G COAD 23 41075555 41075555 + Missense_Mutation SNP A A G TCGA-D5-6898-01A-11D-1924-10 TCGA-D5-6898-10A-01D-1924-10 g.chrX:41075555A>G c.5735A>G c.(5734-5736)gAt>gGt p.D1912G COAD 23 41075559 41075559 + Silent SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chrX:41075559C>T c.5739C>T c.(5737-5739)gaC>gaT p.D1913D COAD 23 41075672 41075672 + Frame_Shift_Del DEL T T - TCGA-D5-6538-01A-11D-1719-10 TCGA-D5-6538-10A-01D-1719-10 g.chrX:41075672delT c.5852delT c.(5851-5853)cttfs p.L1951fs COAD 23 41075683 41075683 + Nonsense_Mutation SNP C C T TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chrX:41075683C>T c.5863C>T c.(5863-5865)Cga>Tga p.R1955* COAD 23 41076578 41076578 + Missense_Mutation SNP G G A TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chrX:41076578G>A c.6191G>A c.(6190-6192)cGt>cAt p.R2064H COAD 23 41077661 41077661 + Missense_Mutation SNP G G T TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chrX:41077661G>T c.6246G>T c.(6244-6246)aaG>aaT p.K2082N COAD 23 41078483 41078483 + Splice_Site SNP A A T TCGA-AZ-4682-01B-01D-1408-10 TCGA-AZ-4682-10A-01D-1408-10 g.chrX:41078483A>T c.6564A>T c.(6562-6564)ttA>ttT p.L2188F COAD 23 41082527 41082527 + Missense_Mutation SNP T T C TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chrX:41082527T>C c.6623T>C c.(6622-6624)gTg>gCg p.V2208A COAD 23 41084097 41084097 + Missense_Mutation SNP A A G TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chrX:41084097A>G c.6854A>G c.(6853-6855)tAt>tGt p.Y2285C COAD 23 41088571 41088572 + Frame_Shift_Ins INS - - T TCGA-CK-5912-01A-11D-1650-10 TCGA-CK-5912-10A-01D-1650-10 g.chrX:41088571_41088572insT c.7127_7128insT c.(7126-7131)tctaagfs p.K2377fs COAD 23 41088663 41088663 + Splice_Site SNP G G A TCGA-CM-5862-01A-01D-1650-10 TCGA-CM-5862-10A-01D-1650-10 g.chrX:41088663G>A c.e42+1 COAD 23 41089034 41089035 + Frame_Shift_Ins INS - - A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chrX:41089034_41089035insA c.7433_7434insA c.(7432-7437)gtaaaafs p.VK2478fs COAD 23 41089035 41089035 + Frame_Shift_Del DEL A A - TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chrX:41089035delA c.7434delA c.(7432-7434)gtafs p.V2478fs COAD 23 41089035 41089035 + Frame_Shift_Del DEL A A - TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chrX:41089035delA c.7434delA c.(7432-7434)gtafs p.V2478fs COAD 23 41089035 41089035 + Frame_Shift_Del DEL A A - TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chrX:41089035delA c.7434delA c.(7432-7434)gtafs p.V2478fs COAD 23 41089035 41089035 + Frame_Shift_Del DEL A A - TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chrX:41089035delA c.7434delA c.(7432-7434)gtafs p.V2478fs COAD 23 41091690 41091690 + Missense_Mutation SNP G G T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chrX:41091690G>T c.7626G>T c.(7624-7626)atG>atT p.M2542I COADREAD 23 40982912 40982912 + Missense_Mutation SNP G G A TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chrX:40982912G>A c.31G>A c.(31-33)Gga>Aga p.G11R COADREAD 23 40988350 40988350 + Missense_Mutation SNP C C A TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chrX:40988350C>A c.194C>A c.(193-195)cCt>cAt p.P65H COADREAD 23 40988387 40988387 + Silent SNP C C T TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chrX:40988387C>T c.231C>T c.(229-231)gaC>gaT p.D77D COADREAD 23 40990744 40990744 + Nonsense_Mutation SNP G G T TCGA-A6-5660-01A-01D-1650-10 TCGA-A6-5660-10A-01D-1650-10 g.chrX:40990744G>T c.277G>T c.(277-279)Gaa>Taa p.E93* COADREAD 23 40996081 40996081 + Missense_Mutation SNP C C T TCGA-CM-6680-01A-11D-1835-10 TCGA-CM-6680-10A-01D-1835-10 g.chrX:40996081C>T c.460C>T c.(460-462)Cgt>Tgt p.R154C COADREAD 23 40996156 40996156 + Missense_Mutation SNP A A C TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chrX:40996156A>C c.535A>C c.(535-537)Aat>Cat p.N179H COADREAD 23 41000437 41000437 + Missense_Mutation SNP A A C TCGA-CK-4950-01A-01D-1719-10 TCGA-CK-4950-10A-01D-1719-10 g.chrX:41000437A>C c.989A>C c.(988-990)aAc>aCc p.N330T COADREAD 23 41007672 41007672 + Silent SNP G G A TCGA-AG-A026-01A-32W-A096-10 TCGA-AG-A026-10A-01W-A096-10 g.chrX:41007672G>A c.1470G>A c.(1468-1470)ctG>ctA p.L490L COADREAD 23 41010222 41010222 + Missense_Mutation SNP C C A TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chrX:41010222C>A c.1675C>A c.(1675-1677)Ctt>Att p.L559I COADREAD 23 41022042 41022042 + Splice_Site SNP G G A TCGA-CM-6165-01A-11D-1650-10 TCGA-CM-6165-10A-01D-1650-10 g.chrX:41022042G>A c.e15-1 COADREAD 23 41025167 41025167 + Missense_Mutation SNP G G T TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chrX:41025167G>T c.2028G>T c.(2026-2028)caG>caT p.Q676H COADREAD 23 41025219 41025219 + Missense_Mutation SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chrX:41025219C>T c.2080C>T c.(2080-2082)Cgt>Tgt p.R694C COADREAD 23 41025392 41025392 + Missense_Mutation SNP A A C TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chrX:41025392A>C c.2253A>C c.(2251-2253)gaA>gaC p.E751D COADREAD 23 41027380 41027380 + Nonsense_Mutation SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chrX:41027380C>T c.2545C>T c.(2545-2547)Cga>Tga p.R849* COADREAD 23 41029361 41029361 + Missense_Mutation SNP G G A TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chrX:41029361G>A c.2750G>A c.(2749-2751)cGa>cAa p.R917Q COADREAD 23 41045782 41045782 + Missense_Mutation SNP A A G TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chrX:41045782A>G c.3571A>G c.(3571-3573)Acc>Gcc p.T1191A COADREAD 23 41045841 41045841 + Silent SNP C C T TCGA-AA-3518-01A-02W-0833-10 TCGA-AA-3518-10A-01W-0833-10 g.chrX:41045841C>T c.3630C>T c.(3628-3630)tcC>tcT p.S1210S COADREAD 23 41047291 41047291 + Missense_Mutation SNP A A C TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chrX:41047291A>C c.3731A>C c.(3730-3732)aAa>aCa p.K1244T COADREAD 23 41055599 41055599 + Missense_Mutation SNP T T C TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chrX:41055599T>C c.4073T>C c.(4072-4074)tTt>tCt p.F1358S COADREAD 23 41055978 41055978 + Missense_Mutation SNP T T G TCGA-CM-5864-01A-01D-1650-10 TCGA-CM-5864-10A-01D-1650-10 g.chrX:41055978T>G c.4220T>G c.(4219-4221)cTt>cGt p.L1407R COADREAD 23 41057839 41057839 + Missense_Mutation SNP A A C TCGA-CM-5864-01A-01D-1650-10 TCGA-CM-5864-10A-01D-1650-10 g.chrX:41057839A>C c.4439A>C c.(4438-4440)aAt>aCt p.N1480T COADREAD 23 41064704 41064704 + Missense_Mutation SNP G G A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chrX:41064704G>A c.4973G>A c.(4972-4974)cGa>cAa p.R1658Q COADREAD 23 41069809 41069809 + Missense_Mutation SNP A A C TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chrX:41069809A>C c.5063A>C c.(5062-5064)gAa>gCa p.E1688A COADREAD 23 41073882 41073882 + Missense_Mutation SNP C C A TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chrX:41073882C>A c.5251C>A c.(5251-5253)Ctt>Att p.L1751I COADREAD 23 41073946 41073946 + Frame_Shift_Del DEL A A - TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chrX:41073946delA c.5315delA c.(5314-5316)gaafs p.E1772fs COADREAD 23 41075428 41075428 + Missense_Mutation SNP G G A TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chrX:41075428G>A c.5608G>A c.(5608-5610)Gta>Ata p.V1870I COADREAD 23 41075439 41075439 + Silent SNP T T G TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chrX:41075439T>G c.5619T>G c.(5617-5619)ggT>ggG p.G1873G COADREAD 23 41075506 41075506 + Missense_Mutation SNP C C T TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chrX:41075506C>T c.5686C>T c.(5686-5688)Cgc>Tgc p.R1896C COADREAD 23 41075555 41075555 + Missense_Mutation SNP A A G TCGA-D5-6537-01A-11D-1719-10 TCGA-D5-6537-10A-01D-1719-10 g.chrX:41075555A>G c.5735A>G c.(5734-5736)gAt>gGt p.D1912G COADREAD 23 41075555 41075555 + Missense_Mutation SNP A A G TCGA-D5-6898-01A-11D-1924-10 TCGA-D5-6898-10A-01D-1924-10 g.chrX:41075555A>G c.5735A>G c.(5734-5736)gAt>gGt p.D1912G COADREAD 23 41075559 41075559 + Silent SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chrX:41075559C>T c.5739C>T c.(5737-5739)gaC>gaT p.D1913D COADREAD 23 41075672 41075672 + Frame_Shift_Del DEL T T - TCGA-D5-6538-01A-11D-1719-10 TCGA-D5-6538-10A-01D-1719-10 g.chrX:41075672delT c.5852delT c.(5851-5853)cttfs p.L1951fs COADREAD 23 41075683 41075683 + Nonsense_Mutation SNP C C T TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chrX:41075683C>T c.5863C>T c.(5863-5865)Cga>Tga p.R1955* COADREAD 23 41076578 41076578 + Missense_Mutation SNP G G A TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chrX:41076578G>A c.6191G>A c.(6190-6192)cGt>cAt p.R2064H COADREAD 23 41077661 41077661 + Missense_Mutation SNP G G T TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chrX:41077661G>T c.6246G>T c.(6244-6246)aaG>aaT p.K2082N COADREAD 23 41078483 41078483 + Splice_Site SNP A A T TCGA-AZ-4682-01B-01D-1408-10 TCGA-AZ-4682-10A-01D-1408-10 g.chrX:41078483A>T c.6564A>T c.(6562-6564)ttA>ttT p.L2188F COADREAD 23 41082527 41082527 + Missense_Mutation SNP T T C TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chrX:41082527T>C c.6623T>C c.(6622-6624)gTg>gCg p.V2208A COADREAD 23 41084097 41084097 + Missense_Mutation SNP A A G TCGA-G4-6588-01A-11D-1771-10 TCGA-G4-6588-10A-01D-1771-10 g.chrX:41084097A>G c.6854A>G c.(6853-6855)tAt>tGt p.Y2285C COADREAD 23 41084340 41084340 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chrX:41084340G>T c.7011G>T c.(7009-7011)ttG>ttT p.L2337F COADREAD 23 41088571 41088572 + Frame_Shift_Ins INS - - T TCGA-CK-5912-01A-11D-1650-10 TCGA-CK-5912-10A-01D-1650-10 g.chrX:41088571_41088572insT c.7127_7128insT c.(7126-7131)tctaagfs p.K2377fs COADREAD 23 41088663 41088663 + Splice_Site SNP G G A TCGA-CM-5862-01A-01D-1650-10 TCGA-CM-5862-10A-01D-1650-10 g.chrX:41088663G>A c.e42+1 COADREAD 23 41089034 41089035 + Frame_Shift_Ins INS - - A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chrX:41089034_41089035insA c.7433_7434insA c.(7432-7437)gtaaaafs p.VK2478fs COADREAD 23 41089035 41089035 + Frame_Shift_Del DEL A A - TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chrX:41089035delA c.7434delA c.(7432-7434)gtafs p.V2478fs COADREAD 23 41089035 41089035 + Frame_Shift_Del DEL A A - TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chrX:41089035delA c.7434delA c.(7432-7434)gtafs p.V2478fs COADREAD 23 41089035 41089035 + Frame_Shift_Del DEL A A - TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chrX:41089035delA c.7434delA c.(7432-7434)gtafs p.V2478fs COADREAD 23 41089035 41089035 + Frame_Shift_Del DEL A A - TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chrX:41089035delA c.7434delA c.(7432-7434)gtafs p.V2478fs COADREAD 23 41091690 41091690 + Missense_Mutation SNP G G T TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chrX:41091690G>T c.7626G>T c.(7624-7626)atG>atT p.M2542I DLBC 23 41056722 41056722 + Missense_Mutation SNP T T A TCGA-FF-A7CR-01A-11D-A382-10 TCGA-FF-A7CR-10A-01D-A385-10 g.chrX:41056722T>A c.4339T>A c.(4339-4341)Ttt>Att p.F1447I DLBC 23 41075218 41075218 + Missense_Mutation SNP T T G TCGA-GS-A9U3-01A-11D-A38X-10 TCGA-GS-A9U3-10A-01D-A38X-10 g.chrX:41075218T>G c.5398T>G c.(5398-5400)Ttt>Gtt p.F1800V ESCA 23 41000020 41000020 + Missense_Mutation SNP A A C TCGA-M9-A5M8-01A-11D-A28B-09 TCGA-M9-A5M8-10A-01D-A28E-09 g.chrX:41000020A>C c.766A>C c.(766-768)Att>Ctt p.I256L ESCA 23 41007638 41007638 + Missense_Mutation SNP C C T TCGA-L5-A891-01A-11D-A36J-09 TCGA-L5-A891-11A-21D-A36M-09 g.chrX:41007638C>T c.1436C>T c.(1435-1437)gCg>gTg p.A479V ESCA 23 41029818 41029818 + Silent SNP T T C TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chrX:41029818T>C c.2973T>C c.(2971-2973)ggT>ggC p.G991G ESCA 23 41057781 41057781 + Splice_Site SNP G G T TCGA-LN-A4A4-01A-11D-A27G-09 TCGA-LN-A4A4-10A-01D-A27G-09 g.chrX:41057781G>T c.4381G>T c.(4381-4383)Gaa>Taa p.E1461* ESCA 23 41057806 41057806 + Missense_Mutation SNP C C T TCGA-ZR-A9CJ-01B-11D-A387-09 TCGA-ZR-A9CJ-10A-01D-A38A-09 g.chrX:41057806C>T c.4406C>T c.(4405-4407)cCt>cTt p.P1469L ESCA 23 41084051 41084051 + Missense_Mutation SNP C C T TCGA-JY-A939-01A-12D-A37C-09 TCGA-JY-A939-10A-01D-A37F-09 g.chrX:41084051C>T c.6808C>T c.(6808-6810)Cca>Tca p.P2270S GBM 23 41075424 41075424 + Silent SNP G G A TCGA-06-5412-01A-01D-1696-08 TCGA-06-5412-10A-01D-1696-08 g.chrX:41075424G>A c.5604G>A c.(5602-5604)gtG>gtA p.V1868V GBM 23 41075440 41075440 + Nonsense_Mutation SNP C C T TCGA-02-0047-01A-01D-1490-08 TCGA-02-0047-10A-01D-1490-08 g.chrX:41075440C>T c.5620C>T c.(5620-5622)Caa>Taa p.Q1874* GBM 23 41075579 41075579 + Missense_Mutation SNP G G C TCGA-27-1838-01A-01D-1494-08 TCGA-27-1838-10A-01D-1494-08 g.chrX:41075579G>C c.5759G>C c.(5758-5760)tGt>tCt p.C1920S GBMLGG 23 41025363 41025363 + Nonsense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:41025363C>T c.2224C>T c.(2224-2226)Cga>Tga p.R742* GBMLGG 23 41027339 41027339 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:41027339G>A c.2504G>A c.(2503-2505)gGt>gAt p.G835D GBMLGG 23 41029755 41029755 + Silent SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:41029755C>A c.2910C>A c.(2908-2910)tcC>tcA p.S970S GBMLGG 23 41043672 41043672 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:41043672C>A c.3302C>A c.(3301-3303)cCt>cAt p.P1101H GBMLGG 23 41048650 41048650 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:41048650C>A c.3899C>A c.(3898-3900)cCa>cAa p.P1300Q GBMLGG 23 41048719 41048719 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:41048719G>A c.3968G>A c.(3967-3969)tGt>tAt p.C1323Y GBMLGG 23 41057788 41057788 + Missense_Mutation SNP T T C TCGA-DU-6410-01A-11D-1893-08 TCGA-DU-6410-10A-01D-1893-08 g.chrX:41057788T>C c.4388T>C c.(4387-4389)aTt>aCt p.I1463T GBMLGG 23 41057976 41057976 + Missense_Mutation SNP A A G TCGA-VM-A8CF-01A-11D-A36O-08 TCGA-VM-A8CF-10A-01D-A367-08 g.chrX:41057976A>G c.4576A>G c.(4576-4578)Atg>Gtg p.M1526V GBMLGG 23 41069807 41069807 + Missense_Mutation SNP A A C TCGA-S9-A7QW-01A-11D-A34A-08 TCGA-S9-A7QW-10A-01D-A34A-08 g.chrX:41069807A>C c.5061A>C c.(5059-5061)ttA>ttC p.L1687F GBMLGG 23 41073892 41073892 + Missense_Mutation SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:41073892T>C c.5261T>C c.(5260-5262)tTg>tCg p.L1754S GBMLGG 23 41075235 41075235 + Missense_Mutation SNP A A T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:41075235A>T c.5415A>T c.(5413-5415)gaA>gaT p.E1805D GBMLGG 23 41075260 41075260 + Missense_Mutation SNP G G A TCGA-DB-A64L-01A-11D-A29Q-08 TCGA-DB-A64L-10A-01D-A29Q-08 g.chrX:41075260G>A c.5440G>A c.(5440-5442)Gat>Aat p.D1814N GBMLGG 23 41075424 41075424 + Silent SNP G G A TCGA-06-5412-01A-01D-1696-08 TCGA-06-5412-10A-01D-1696-08 g.chrX:41075424G>A c.5604G>A c.(5602-5604)gtG>gtA p.V1868V GBMLGG 23 41075440 41075440 + Nonsense_Mutation SNP C C T TCGA-02-0047-01A-01D-1490-08 TCGA-02-0047-10A-01D-1490-08 g.chrX:41075440C>T c.5620C>T c.(5620-5622)Caa>Taa p.Q1874* GBMLGG 23 41075579 41075579 + Missense_Mutation SNP G G C TCGA-27-1838-01A-01D-1494-08 TCGA-27-1838-10A-01D-1494-08 g.chrX:41075579G>C c.5759G>C c.(5758-5760)tGt>tCt p.C1920S GBMLGG 23 41084138 41084138 + Missense_Mutation SNP A A G TCGA-DB-A4XD-01A-11D-A27K-08 TCGA-DB-A4XD-10A-01D-A27N-08 g.chrX:41084138A>G c.6895A>G c.(6895-6897)Acc>Gcc p.T2299A GBMLGG 23 41088882 41088884 + In_Frame_Del DEL AAG AAG - TCGA-HW-7490-01A-11D-2024-08 TCGA-HW-7490-10A-01D-2024-08 g.chrX:41088882_41088884delAAG c.7281_7283delAAG c.(7279-7284)gaaaga>gaa p.R2429del GBMLGG 23 41091710 41091710 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:41091710G>A c.7646G>A c.(7645-7647)gGc>gAc p.G2549D HNSC 23 40988323 40988323 + Missense_Mutation SNP C C T TCGA-DQ-5625-01A-01D-1870-08 TCGA-DQ-5625-10A-01D-1870-08 g.chrX:40988323C>T c.167C>T c.(166-168)gCc>gTc p.A56V HNSC 23 40990715 40990715 + Missense_Mutation SNP G G T TCGA-CV-7433-01A-11D-2129-08 TCGA-CV-7433-10A-01D-2129-08 g.chrX:40990715G>T c.248G>T c.(247-249)cGa>cTa p.R83L HNSC 23 40994016 40994016 + Missense_Mutation SNP C C T TCGA-CV-A45U-01A-12D-A24D-08 TCGA-CV-A45U-10A-01D-A24F-08 g.chrX:40994016C>T c.361C>T c.(361-363)Cgt>Tgt p.R121C HNSC 23 41000592 41000592 + Missense_Mutation SNP G G A TCGA-CV-6961-01A-21D-1912-08 TCGA-CV-6961-10A-01D-1912-08 g.chrX:41000592G>A c.1069G>A c.(1069-1071)Gaa>Aaa p.E357K HNSC 23 41000615 41000616 + Frame_Shift_Ins INS - - CACCTTA TCGA-UP-A6WW-01A-12D-A34J-08 TCGA-UP-A6WW-10B-01D-A34M-08 g.chrX:41000615_41000616insCACCTTA c.1092_1093insCACCTTA c.(1093-1095)gtafs p.V365fs HNSC 23 41000616 41000616 + Missense_Mutation SNP G G T TCGA-UP-A6WW-01A-12D-A34J-08 TCGA-UP-A6WW-10B-01D-A34M-08 g.chrX:41000616G>T c.1093G>T c.(1093-1095)Gta>Tta p.V365L HNSC 23 41000632 41000632 + Missense_Mutation SNP A A G TCGA-CN-5358-01A-01D-1512-08 TCGA-CN-5358-10A-01D-1512-08 g.chrX:41000632A>G c.1109A>G c.(1108-1110)cAt>cGt p.H370R HNSC 23 41002598 41002598 + Nonsense_Mutation SNP C C T TCGA-CV-A463-01A-11D-A25Y-08 TCGA-CV-A463-10A-01D-A25Y-08 g.chrX:41002598C>T c.1216C>T c.(1216-1218)Cag>Tag p.Q406* HNSC 23 41007694 41007694 + Missense_Mutation SNP G G A TCGA-BB-A5HY-01A-11D-A28R-08 TCGA-BB-A5HY-10A-01D-A28U-08 g.chrX:41007694G>A c.1492G>A c.(1492-1494)Gat>Aat p.D498N HNSC 23 41007737 41007737 + Missense_Mutation SNP G G T TCGA-CN-4742-01A-02D-1512-08 TCGA-CN-4742-10A-01D-1512-08 g.chrX:41007737G>T c.1535G>T c.(1534-1536)tGg>tTg p.W512L HNSC 23 41027443 41027443 + Nonsense_Mutation SNP G G T TCGA-MT-A67F-01A-11D-A30E-08 TCGA-MT-A67F-10A-01D-A30H-08 g.chrX:41027443G>T c.2608G>T c.(2608-2610)Gag>Tag p.E870* HNSC 23 41027468 41027468 + Missense_Mutation SNP C C T TCGA-CV-A468-01A-11D-A25Y-08 TCGA-CV-A468-10A-01D-A25Y-08 g.chrX:41027468C>T c.2633C>T c.(2632-2634)tCg>tTg p.S878L HNSC 23 41031206 41031206 + Missense_Mutation SNP C C G TCGA-CV-7248-01A-11D-2012-08 TCGA-CV-7248-10A-01D-2013-08 g.chrX:41031206C>G c.3143C>G c.(3142-3144)cCg>cGg p.P1048R HNSC 23 41048594 41048594 + Silent SNP C C T TCGA-CR-7395-01A-11D-2012-08 TCGA-CR-7395-10A-01D-2013-08 g.chrX:41048594C>T c.3843C>T c.(3841-3843)gaC>gaT p.D1281D HNSC 23 41056744 41056744 + Missense_Mutation SNP G G C TCGA-T2-A6X2-01A-12D-A34J-08 TCGA-T2-A6X2-10B-01D-A34M-08 g.chrX:41056744G>C c.4361G>C c.(4360-4362)gGa>gCa p.G1454A HNSC 23 41060380 41060380 + Frame_Shift_Del DEL G G - TCGA-HD-A634-01A-11D-A28R-08 TCGA-HD-A634-10A-01D-A28U-08 g.chrX:41060380delG c.4671delG c.(4669-4671)gtgfs p.V1557fs HNSC 23 41069829 41069829 + Missense_Mutation SNP G G T TCGA-CR-7374-01A-11D-2012-08 TCGA-CR-7374-10A-01D-2013-08 g.chrX:41069829G>T c.5083G>T c.(5083-5085)Gat>Tat p.D1695Y HNSC 23 41073879 41073879 + Frame_Shift_Del DEL C C - TCGA-D6-A6EK-01A-11D-A31L-08 TCGA-D6-A6EK-10A-01D-A31J-08 g.chrX:41073879delC c.5248delC c.(5248-5250)cttfs p.L1751fs HNSC 23 41075168 41075168 + Missense_Mutation SNP G G A TCGA-H7-7774-01A-21D-2078-08 TCGA-H7-7774-10A-01D-2078-08 g.chrX:41075168G>A c.5348G>A c.(5347-5349)cGc>cAc p.R1783H HNSC 23 41075704 41075704 + Missense_Mutation SNP G G C TCGA-CN-5369-01A-01D-1434-08 TCGA-CN-5369-10A-01D-1434-08 g.chrX:41075704G>C c.5884G>C c.(5884-5886)Gat>Cat p.D1962H HNSC 23 41077795 41077795 + Missense_Mutation SNP C C T TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chrX:41077795C>T c.6380C>T c.(6379-6381)tCc>tTc p.S2127F HNSC 23 41077799 41077799 + Silent SNP G G A TCGA-CQ-6224-01A-11D-1912-08 TCGA-CQ-6224-10A-01D-1912-08 g.chrX:41077799G>A c.6384G>A c.(6382-6384)ttG>ttA p.L2128L HNSC 23 41077827 41077827 + Missense_Mutation SNP G G A TCGA-CR-7364-01A-11D-2012-08 TCGA-CR-7364-10A-01D-2013-08 g.chrX:41077827G>A c.6412G>A c.(6412-6414)Gcc>Acc p.A2138T HNSC 23 41082519 41082519 + Missense_Mutation SNP T T A TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chrX:41082519T>A c.6615T>A c.(6613-6615)ttT>ttA p.F2205L HNSC 23 41088557 41088563 + Frame_Shift_Del DEL CACAATC CACAATC - TCGA-D6-6517-01A-11D-1870-08 TCGA-D6-6517-10A-01D-1870-08 g.chrX:41088557_41088563delCACAATC c.7113_7119delCACAATC c.(7111-7119)gacacaatcfs p.DTI2371fs HNSC 23 41088843 41088843 + Silent SNP G G A TCGA-IQ-A61K-01A-11D-A30E-08 TCGA-IQ-A61K-10A-01D-A30H-08 g.chrX:41088843G>A c.7242G>A c.(7240-7242)aaG>aaA p.K2414K HNSC 23 41088907 41088907 + Nonsense_Mutation SNP C C T TCGA-P3-A5QF-01A-11D-A28R-08 TCGA-P3-A5QF-10A-01D-A28U-08 g.chrX:41088907C>T c.7306C>T c.(7306-7308)Cag>Tag p.Q2436* HNSC 23 41088917 41088919 + In_Frame_Del DEL ACA ACA - TCGA-IQ-7631-01A-11D-2078-08 TCGA-IQ-7631-10A-01D-2078-08 g.chrX:41088917_41088919delACA c.7316_7318delACA c.(7315-7320)tacaac>tac p.N2441del HNSC 23 41089764 41089764 + Missense_Mutation SNP A A G TCGA-UF-A71D-01A-12D-A34J-08 TCGA-UF-A71D-10B-01D-A34M-08 g.chrX:41089764A>G c.7490A>G c.(7489-7491)gAc>gGc p.D2497G KICH 23 41002593 41002593 + Missense_Mutation SNP T T G TCGA-KL-8323-01A-21D-2310-10 TCGA-KL-8323-11A-01D-2310-10 g.chrX:41002593T>G c.1211T>G c.(1210-1212)cTt>cGt p.L404R KICH 23 41010226 41010226 + Missense_Mutation SNP G G T TCGA-KM-8477-01A-11D-2310-10 TCGA-KM-8477-10A-01D-2311-10 g.chrX:41010226G>T c.1679G>T c.(1678-1680)cGc>cTc p.R560L KICH 23 41029423 41029423 + Missense_Mutation SNP G G A TCGA-KL-8331-01A-11D-2310-10 TCGA-KL-8331-11A-01D-2310-10 g.chrX:41029423G>A c.2812G>A c.(2812-2814)Ggt>Agt p.G938S KICH 23 41088984 41088985 + Frame_Shift_Ins INS - - A TCGA-KL-8334-01A-11D-2310-10 TCGA-KL-8334-11A-01D-2310-10 g.chrX:41088984_41088985insA c.7383_7384insA c.(7384-7386)agtfs p.S2462fs KICH 23 41088985 41088986 + Frame_Shift_Ins INS - - A TCGA-KL-8334-01A-11D-2310-10 TCGA-KL-8334-11A-01D-2310-10 g.chrX:41088985_41088986insA c.7384_7385insA c.(7384-7386)agtfs p.S2462fs KIPAN 23 40999924 40999924 + Missense_Mutation SNP C C A TCGA-B9-5156-01A-01D-1589-08 TCGA-B9-5156-10A-01D-1589-08 g.chrX:40999924C>A c.670C>A c.(670-672)Ctt>Att p.L224I KIPAN 23 41002593 41002593 + Missense_Mutation SNP T T G TCGA-KL-8323-01A-21D-2310-10 TCGA-KL-8323-11A-01D-2310-10 g.chrX:41002593T>G c.1211T>G c.(1210-1212)cTt>cGt p.L404R KIPAN 23 41010226 41010226 + Missense_Mutation SNP G G T TCGA-KM-8477-01A-11D-2310-10 TCGA-KM-8477-10A-01D-2311-10 g.chrX:41010226G>T c.1679G>T c.(1678-1680)cGc>cTc p.R560L KIPAN 23 41025293 41025293 + Missense_Mutation SNP C C A TCGA-CJ-4875-01A-01D-1373-10 TCGA-CJ-4875-11A-01D-1373-10 g.chrX:41025293C>A c.2154C>A c.(2152-2154)gaC>gaA p.D718E KIPAN 23 41025335 41025335 + Silent SNP A A G TCGA-CZ-4861-01A-01D-1373-10 TCGA-CZ-4861-11A-01D-1373-10 g.chrX:41025335A>G c.2196A>G c.(2194-2196)ttA>ttG p.L732L KIPAN 23 41029423 41029423 + Missense_Mutation SNP G G A TCGA-KL-8331-01A-11D-2310-10 TCGA-KL-8331-11A-01D-2310-10 g.chrX:41029423G>A c.2812G>A c.(2812-2814)Ggt>Agt p.G938S KIPAN 23 41043810 41043810 + Missense_Mutation SNP C C T TCGA-B9-A69E-01A-11D-A31X-10 TCGA-B9-A69E-10A-01D-A31X-10 g.chrX:41043810C>T c.3440C>T c.(3439-3441)gCc>gTc p.A1147V KIPAN 23 41047253 41047253 + Silent SNP A A G TCGA-BP-4160-01A-02D-1366-10 TCGA-BP-4160-11A-01D-1806-10 g.chrX:41047253A>G c.3693A>G c.(3691-3693)agA>agG p.R1231R KIPAN 23 41077774 41077774 + Missense_Mutation SNP T T C TCGA-CJ-4881-01A-01D-1373-10 TCGA-CJ-4881-11A-01D-1373-10 g.chrX:41077774T>C c.6359T>C c.(6358-6360)aTa>aCa p.I2120T KIPAN 23 41088595 41088595 + Missense_Mutation SNP C C A TCGA-BP-5168-01A-01D-1421-08 TCGA-BP-5168-11A-01D-1421-08 g.chrX:41088595C>A c.7151C>A c.(7150-7152)gCa>gAa p.A2384E KIPAN 23 41088984 41088985 + Frame_Shift_Ins INS - - A TCGA-KL-8334-01A-11D-2310-10 TCGA-KL-8334-11A-01D-2310-10 g.chrX:41088984_41088985insA c.7383_7384insA c.(7384-7386)agtfs p.S2462fs KIPAN 23 41088985 41088986 + Frame_Shift_Ins INS - - A TCGA-KL-8334-01A-11D-2310-10 TCGA-KL-8334-11A-01D-2310-10 g.chrX:41088985_41088986insA c.7384_7385insA c.(7384-7386)agtfs p.S2462fs KIPAN 23 41091721 41091721 + Missense_Mutation SNP C C G TCGA-A3-3370-01A-02D-1421-08 TCGA-A3-3370-11A-01D-1421-08 g.chrX:41091721C>G c.7657C>G c.(7657-7659)Caa>Gaa p.Q2553E KIRC 23 41025293 41025293 + Missense_Mutation SNP C C A TCGA-CJ-4875-01A-01D-1373-10 TCGA-CJ-4875-11A-01D-1373-10 g.chrX:41025293C>A c.2154C>A c.(2152-2154)gaC>gaA p.D718E KIRC 23 41025335 41025335 + Silent SNP A A G TCGA-CZ-4861-01A-01D-1373-10 TCGA-CZ-4861-11A-01D-1373-10 g.chrX:41025335A>G c.2196A>G c.(2194-2196)ttA>ttG p.L732L KIRC 23 41047253 41047253 + Silent SNP A A G TCGA-BP-4160-01A-02D-1366-10 TCGA-BP-4160-11A-01D-1806-10 g.chrX:41047253A>G c.3693A>G c.(3691-3693)agA>agG p.R1231R KIRC 23 41077774 41077774 + Missense_Mutation SNP T T C TCGA-CJ-4881-01A-01D-1373-10 TCGA-CJ-4881-11A-01D-1373-10 g.chrX:41077774T>C c.6359T>C c.(6358-6360)aTa>aCa p.I2120T KIRC 23 41088595 41088595 + Missense_Mutation SNP C C A TCGA-BP-5168-01A-01D-1421-08 TCGA-BP-5168-11A-01D-1421-08 g.chrX:41088595C>A c.7151C>A c.(7150-7152)gCa>gAa p.A2384E KIRC 23 41091721 41091721 + Missense_Mutation SNP C C G TCGA-A3-3370-01A-02D-1421-08 TCGA-A3-3370-11A-01D-1421-08 g.chrX:41091721C>G c.7657C>G c.(7657-7659)Caa>Gaa p.Q2553E KIRP 23 40999924 40999924 + Missense_Mutation SNP C C A TCGA-B9-5156-01A-01D-1589-08 TCGA-B9-5156-10A-01D-1589-08 g.chrX:40999924C>A c.670C>A c.(670-672)Ctt>Att p.L224I KIRP 23 41043810 41043810 + Missense_Mutation SNP C C T TCGA-B9-A69E-01A-11D-A31X-10 TCGA-B9-A69E-10A-01D-A31X-10 g.chrX:41043810C>T c.3440C>T c.(3439-3441)gCc>gTc p.A1147V LAML 23 41010296 41010296 + Silent SNP G G A TCGA-AB-3001-03A-01D-0739-09 TCGA-AB-3001-11A-01D-0739-09 g.chrX:41010296G>A c.1749G>A c.(1747-1749)gcG>gcA p.A583A LAML 23 41027390 41027391 + Frame_Shift_Ins INS - - CG TCGA-AB-2934-03A-01W-0755-09 TCGA-AB-2934-11A-01W-0755-09 g.chrX:41027390_41027391insCG c.2555_2556insCG c.(2554-2559)cgagtafs p.V853fs LGG 23 41025363 41025363 + Nonsense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:41025363C>T c.2224C>T c.(2224-2226)Cga>Tga p.R742* LGG 23 41027339 41027339 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:41027339G>A c.2504G>A c.(2503-2505)gGt>gAt p.G835D LGG 23 41029755 41029755 + Silent SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:41029755C>A c.2910C>A c.(2908-2910)tcC>tcA p.S970S LGG 23 41043672 41043672 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:41043672C>A c.3302C>A c.(3301-3303)cCt>cAt p.P1101H LGG 23 41048650 41048650 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:41048650C>A c.3899C>A c.(3898-3900)cCa>cAa p.P1300Q LGG 23 41048719 41048719 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:41048719G>A c.3968G>A c.(3967-3969)tGt>tAt p.C1323Y LGG 23 41057788 41057788 + Missense_Mutation SNP T T C TCGA-DU-6410-01A-11D-1893-08 TCGA-DU-6410-10A-01D-1893-08 g.chrX:41057788T>C c.4388T>C c.(4387-4389)aTt>aCt p.I1463T LGG 23 41057976 41057976 + Missense_Mutation SNP A A G TCGA-VM-A8CF-01A-11D-A36O-08 TCGA-VM-A8CF-10A-01D-A367-08 g.chrX:41057976A>G c.4576A>G c.(4576-4578)Atg>Gtg p.M1526V LGG 23 41069807 41069807 + Missense_Mutation SNP A A C TCGA-S9-A7QW-01A-11D-A34A-08 TCGA-S9-A7QW-10A-01D-A34A-08 g.chrX:41069807A>C c.5061A>C c.(5059-5061)ttA>ttC p.L1687F LGG 23 41073892 41073892 + Missense_Mutation SNP T T C TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:41073892T>C c.5261T>C c.(5260-5262)tTg>tCg p.L1754S LGG 23 41075235 41075235 + Missense_Mutation SNP A A T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:41075235A>T c.5415A>T c.(5413-5415)gaA>gaT p.E1805D LGG 23 41075260 41075260 + Missense_Mutation SNP G G A TCGA-DB-A64L-01A-11D-A29Q-08 TCGA-DB-A64L-10A-01D-A29Q-08 g.chrX:41075260G>A c.5440G>A c.(5440-5442)Gat>Aat p.D1814N LGG 23 41084138 41084138 + Missense_Mutation SNP A A G TCGA-DB-A4XD-01A-11D-A27K-08 TCGA-DB-A4XD-10A-01D-A27N-08 g.chrX:41084138A>G c.6895A>G c.(6895-6897)Acc>Gcc p.T2299A LGG 23 41088882 41088884 + In_Frame_Del DEL AAG AAG - TCGA-HW-7490-01A-11D-2024-08 TCGA-HW-7490-10A-01D-2024-08 g.chrX:41088882_41088884delAAG c.7281_7283delAAG c.(7279-7284)gaaaga>gaa p.R2429del LGG 23 41091710 41091710 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:41091710G>A c.7646G>A c.(7645-7647)gGc>gAc p.G2549D LIHC 23 41002598 41002598 + Missense_Mutation SNP C C G TCGA-MI-A75C-01A-11D-A32G-10 TCGA-MI-A75C-10A-01D-A32G-10 g.chrX:41002598C>G c.1216C>G c.(1216-1218)Cag>Gag p.Q406E LIHC 23 41022048 41022048 + Nonsense_Mutation SNP G G T TCGA-ZS-A9CE-01A-11D-A36X-10 TCGA-ZS-A9CE-10A-01D-A370-10 g.chrX:41022048G>T c.1903G>T c.(1903-1905)Gaa>Taa p.E635* LIHC 23 41043827 41043827 + Frame_Shift_Del DEL A A - TCGA-G3-A3CJ-01A-11D-A20W-10 TCGA-G3-A3CJ-10A-01D-A20W-10 g.chrX:41043827delA c.3457delA c.(3457-3459)aaafs p.K1153fs LIHC 23 41048571 41048571 + Missense_Mutation SNP G G A TCGA-DD-AACD-01A-11D-A40R-10 TCGA-DD-AACD-10A-01D-A40U-10 g.chrX:41048571G>A c.3820G>A c.(3820-3822)Ggc>Agc p.G1274S LIHC 23 41069765 41069765 + Silent SNP T T A TCGA-UB-A7ME-01A-11D-A33K-10 TCGA-UB-A7ME-10A-01D-A33K-10 g.chrX:41069765T>A c.5019T>A c.(5017-5019)ctT>ctA p.L1673L LIHC 23 41069767 41069767 + Frame_Shift_Del DEL G G - TCGA-DD-A39Y-01A-11D-A20W-10 TCGA-DD-A39Y-11A-11D-A20W-10 g.chrX:41069767delG c.5021delG c.(5020-5022)tggfs p.W1674fs LIHC 23 41069811 41069811 + Frame_Shift_Del DEL T T - TCGA-DD-A1EG-01A-11D-A20W-10 TCGA-DD-A1EG-10A-01D-A20W-10 g.chrX:41069811delT c.5065delT c.(5065-5067)tttfs p.F1690fs LIHC 23 41075386 41075386 + Nonsense_Mutation SNP G G T TCGA-DD-AADE-01A-11D-A40R-10 TCGA-DD-AADE-10A-01D-A40U-10 g.chrX:41075386G>T c.5566G>T c.(5566-5568)Gag>Tag p.E1856* LIHC 23 41075804 41075804 + Missense_Mutation SNP A A G TCGA-DD-A39Y-01A-11D-A20W-10 TCGA-DD-A39Y-11A-11D-A20W-10 g.chrX:41075804A>G c.5984A>G c.(5983-5985)aAc>aGc p.N1995S LIHC 23 41088999 41088999 + Silent SNP A A G TCGA-CC-A3MA-01A-11D-A20W-10 TCGA-CC-A3MA-10A-01D-A20W-10 g.chrX:41088999A>G c.7398A>G c.(7396-7398)acA>acG p.T2466T LUAD 23 40994008 40994008 + Missense_Mutation SNP G G A TCGA-69-7979-01A-11D-2184-08 TCGA-69-7979-10A-01D-2184-08 g.chrX:40994008G>A c.353G>A c.(352-354)cGa>cAa p.R118Q LUAD 23 40999908 40999908 + Splice_Site SNP G G C TCGA-L9-A443-01A-12D-A24D-08 TCGA-L9-A443-10A-01D-A24F-08 g.chrX:40999908G>C c.e7-1 LUAD 23 41000347 41000347 + Missense_Mutation SNP A A G TCGA-55-1592-01A-01D-0969-08 TCGA-55-1592-11A-01D-0969-08 g.chrX:41000347A>G c.899A>G c.(898-900)aAt>aGt p.N300S LUAD 23 41000658 41000658 + Missense_Mutation SNP G G C TCGA-64-5781-01A-01D-1625-08 TCGA-64-5781-10A-01D-1625-08 g.chrX:41000658G>C c.1135G>C c.(1135-1137)Gag>Cag p.E379Q LUAD 23 41010268 41010268 + Missense_Mutation SNP G G C TCGA-NJ-A4YF-01A-12D-A25L-08 TCGA-NJ-A4YF-10A-01D-A25L-08 g.chrX:41010268G>C c.1721G>C c.(1720-1722)aGa>aCa p.R574T LUAD 23 41012324 41012324 + Silent SNP A A G TCGA-05-4430-01A-02D-1265-08 TCGA-05-4430-10A-01D-1265-08 g.chrX:41012324A>G c.1887A>G c.(1885-1887)ctA>ctG p.L629L LUAD 23 41025388 41025388 + Missense_Mutation SNP G G A TCGA-38-4630-01A-01D-1265-08 TCGA-38-4630-11A-01D-1265-08 g.chrX:41025388G>A c.2249G>A c.(2248-2250)cGa>cAa p.R750Q LUAD 23 41025463 41025463 + Missense_Mutation SNP G G T TCGA-05-4396-01A-21D-1855-08 TCGA-05-4396-10A-01D-1855-08 g.chrX:41025463G>T c.2324G>T c.(2323-2325)tGg>tTg p.W775L LUAD 23 41029419 41029419 + Silent SNP G G T TCGA-86-A456-01A-11D-A24D-08 TCGA-86-A456-10A-01D-A24F-08 g.chrX:41029419G>T c.2808G>T c.(2806-2808)gtG>gtT p.V936V LUAD 23 41029762 41029762 + Missense_Mutation SNP C C T TCGA-44-6147-01A-11D-1753-08 TCGA-44-6147-10A-01D-1753-08 g.chrX:41029762C>T c.2917C>T c.(2917-2919)Cct>Tct p.P973S LUAD 23 41043333 41043333 + Missense_Mutation SNP C C A TCGA-69-A59K-01A-11D-A25L-08 TCGA-69-A59K-10A-01D-A25L-08 g.chrX:41043333C>A c.3231C>A c.(3229-3231)gaC>gaA p.D1077E LUAD 23 41043661 41043661 + Silent SNP C C T TCGA-44-2656-01A-02D-0969-08 TCGA-44-2656-10A-01D-0969-08 g.chrX:41043661C>T c.3291C>T c.(3289-3291)gcC>gcT p.A1097A LUAD 23 41055512 41055512 + Missense_Mutation SNP G G A TCGA-71-8520-01A-11D-2393-08 TCGA-71-8520-10A-01D-2393-08 g.chrX:41055512G>A c.3986G>A c.(3985-3987)cGt>cAt p.R1329H LUAD 23 41055569 41055569 + Missense_Mutation SNP G G T TCGA-17-Z055-01A-01W-0747-08 TCGA-17-Z055-11A-01W-0747-08 g.chrX:41055569G>T c.4043G>T c.(4042-4044)cGg>cTg p.R1348L LUAD 23 41056749 41056749 + Missense_Mutation SNP G G A TCGA-MP-A4TH-01A-31D-A25L-08 TCGA-MP-A4TH-10A-01D-A25L-08 g.chrX:41056749G>A c.4366G>A c.(4366-4368)Gct>Act p.A1456T LUAD 23 41057842 41057842 + Missense_Mutation SNP G G T TCGA-17-Z022-01A-01W-0746-08 TCGA-17-Z022-11A-01W-0746-08 g.chrX:41057842G>T c.4442G>T c.(4441-4443)gGa>gTa p.G1481V LUAD 23 41069770 41069770 + Missense_Mutation SNP G G T TCGA-55-8620-01A-11D-2393-08 TCGA-55-8620-10A-01D-2393-08 g.chrX:41069770G>T c.5024G>T c.(5023-5025)gGt>gTt p.G1675V LUAD 23 41073863 41073863 + Silent SNP T T A TCGA-44-3919-01A-02D-1458-08 TCGA-44-3919-10A-01D-1458-08 g.chrX:41073863T>A c.5232T>A c.(5230-5232)atT>atA p.I1744I LUAD 23 41075524 41075524 + Missense_Mutation SNP G G A TCGA-17-Z023-01A-01W-0746-08 TCGA-17-Z023-11A-01W-0746-08 g.chrX:41075524G>A c.5704G>A c.(5704-5706)Gat>Aat p.D1902N LUAD 23 41075556 41075556 + Silent SNP T T C TCGA-86-A456-01A-11D-A24D-08 TCGA-86-A456-10A-01D-A24F-08 g.chrX:41075556T>C c.5736T>C c.(5734-5736)gaT>gaC p.D1912D LUAD 23 41075707 41075707 + Missense_Mutation SNP G G C TCGA-17-Z057-01A-01W-0747-08 TCGA-17-Z057-11A-01W-0747-08 g.chrX:41075707G>C c.5887G>C c.(5887-5889)Gat>Cat p.D1963H LUAD 23 41075817 41075817 + Missense_Mutation SNP G G A TCGA-05-4427-01A-21D-1855-08 TCGA-05-4427-10A-01D-1855-08 g.chrX:41075817G>A c.5997G>A c.(5995-5997)atG>atA p.M1999I LUAD 23 41077680 41077680 + Missense_Mutation SNP G G T TCGA-69-7763-01A-11D-2167-08 TCGA-69-7763-10A-01D-2167-08 g.chrX:41077680G>T c.6265G>T c.(6265-6267)Gct>Tct p.A2089S LUAD 23 41082625 41082625 + Missense_Mutation SNP G G T TCGA-50-5930-01A-11D-1753-08 TCGA-50-5930-11A-01D-1753-08 g.chrX:41082625G>T c.6721G>T c.(6721-6723)Gtc>Ttc p.V2241F LUAD 23 41084348 41084348 + Frame_Shift_Del DEL T T - TCGA-69-7978-01A-11D-2184-08 TCGA-69-7978-10A-01D-2184-08 g.chrX:41084348delT c.7019delT c.(7018-7020)cttfs p.L2341fs LUAD 23 41088852 41088852 + Missense_Mutation SNP G G T TCGA-91-6831-01A-11D-1855-08 TCGA-91-6831-11A-02D-1855-08 g.chrX:41088852G>T c.7251G>T c.(7249-7251)tgG>tgT p.W2417C LUAD 23 41088907 41088907 + Nonsense_Mutation SNP C C T TCGA-50-6594-01A-11D-1753-08 TCGA-50-6594-11A-01D-1753-08 g.chrX:41088907C>T c.7306C>T c.(7306-7308)Cag>Tag p.Q2436* LUAD 23 41089775 41089775 + Missense_Mutation SNP C C A TCGA-55-7911-01A-11D-2167-08 TCGA-55-7911-10A-01D-2167-08 g.chrX:41089775C>A c.7501C>A c.(7501-7503)Cca>Aca p.P2501T LUAD 23 41091776 41091776 + Silent SNP G G A TCGA-MN-A4N4-01A-12D-A24P-08 TCGA-MN-A4N4-10A-01D-A24P-08 g.chrX:41091776G>A c.7712G>A c.(7711-7713)tGa>tAa p.*2571* LUSC 23 40994071 40994071 + Missense_Mutation SNP G G T TCGA-66-2734-01A-01D-0983-08 TCGA-66-2734-11A-01D-0983-08 g.chrX:40994071G>T c.416G>T c.(415-417)gGc>gTc p.G139V LUSC 23 41000371 41000371 + Nonsense_Mutation SNP C C A TCGA-66-2763-01A-01D-1522-08 TCGA-66-2763-11A-01D-1522-08 g.chrX:41000371C>A c.923C>A c.(922-924)tCa>tAa p.S308* LUSC 23 41010252 41010252 + Missense_Mutation SNP G G C TCGA-43-5668-01A-01D-1632-08 TCGA-43-5668-11A-01D-1632-08 g.chrX:41010252G>C c.1705G>C c.(1705-1707)Gca>Cca p.A569P LUSC 23 41026799 41026799 + Missense_Mutation SNP C C T TCGA-66-2787-01A-01D-0983-08 TCGA-66-2787-11A-01D-0983-08 g.chrX:41026799C>T c.2393C>T c.(2392-2394)aCg>aTg p.T798M LUSC 23 41056655 41056655 + Missense_Mutation SNP G G C TCGA-34-5929-01A-11D-1817-08 TCGA-34-5929-11A-01D-1817-08 g.chrX:41056655G>C c.4272G>C c.(4270-4272)gaG>gaC p.E1424D LUSC 23 41064718 41064718 + Missense_Mutation SNP G G C TCGA-34-5929-01A-11D-1817-08 TCGA-34-5929-11A-01D-1817-08 g.chrX:41064718G>C c.4987G>C c.(4987-4989)Gtg>Ctg p.V1663L LUSC 23 41075504 41075505 + Frame_Shift_Ins INS - - T TCGA-66-2759-01A-01D-1522-08 TCGA-66-2759-11A-01D-1522-08 g.chrX:41075504_41075505insT c.5684_5685insT c.(5683-5688)aatcgcfs p.R1896fs LUSC 23 41075634 41075635 + Frame_Shift_Ins INS - - T TCGA-66-2768-01A-01D-1522-08 TCGA-66-2768-11A-01D-1522-08 g.chrX:41075634_41075635insT c.5814_5815insT c.(5815-5817)tacfs p.Y1939fs LUSC 23 41075775 41075775 + Silent SNP A A T TCGA-66-2786-01A-01D-1522-08 TCGA-66-2786-11A-01D-1522-08 g.chrX:41075775A>T c.5955A>T c.(5953-5955)tcA>tcT p.S1985S LUSC 23 41078486 41078486 + Splice_Site SNP T T A TCGA-39-5024-01A-21D-1817-08 TCGA-39-5024-11A-01D-1817-08 g.chrX:41078486T>A c.e38+2 OV 23 40988342 40988342 + Missense_Mutation SNP T T A TCGA-13-2071-01A-02D-1526-09 TCGA-13-2071-10A-01D-1526-09 g.chrX:40988342T>A c.186T>A c.(184-186)gaT>gaA p.D62E OV 23 40990733 40990733 + Missense_Mutation SNP T T G TCGA-61-1727-01A-01W-0639-09 TCGA-61-1727-11A-01W-0639-09 g.chrX:40990733T>G c.266T>G c.(265-267)tTg>tGg p.L89W OV 23 41000577 41000577 + Missense_Mutation SNP A A G TCGA-61-1900-01A-01W-0639-09 TCGA-61-1900-11A-01W-0640-09 g.chrX:41000577A>G c.1054A>G c.(1054-1056)Atg>Gtg p.M352V OV 23 41075555 41075555 + Missense_Mutation SNP A A G TCGA-61-1995-01A-01W-0722-08 TCGA-61-1995-11A-01W-0722-08 g.chrX:41075555A>G c.5735A>G c.(5734-5736)gAt>gGt p.D1912G PAAD 23 41000309 41000309 + Silent SNP A A G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chrX:41000309A>G c.861A>G c.(859-861)gaA>gaG p.E287E PAAD 23 41029282 41029282 + Nonsense_Mutation SNP C C T TCGA-XD-AAUI-01A-42D-A40W-08 TCGA-XD-AAUI-10A-01D-A40W-08 g.chrX:41029282C>T c.2671C>T c.(2671-2673)Cga>Tga p.R891* PAAD 23 41031200 41031200 + Missense_Mutation SNP T T G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chrX:41031200T>G c.3137T>G c.(3136-3138)cTt>cGt p.L1046R PAAD 23 41045841 41045841 + Silent SNP C C A TCGA-HZ-A77Q-01A-11D-A36O-08 TCGA-HZ-A77Q-10A-01D-A367-08 g.chrX:41045841C>A c.3630C>A c.(3628-3630)tcC>tcA p.S1210S PAAD 23 41075627 41075627 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chrX:41075627G>A c.5807G>A c.(5806-5808)cGt>cAt p.R1936H PCPG 23 40990708 40990708 + Splice_Site SNP A A G TCGA-WB-A818-01A-11D-A35I-08 TCGA-WB-A818-10A-01D-A35G-08 g.chrX:40990708A>G c.e4-1 PCPG 23 41012243 41012246 + Frame_Shift_Del DEL AATC AATC - TCGA-QR-A70U-01A-11D-A35D-08 TCGA-QR-A70U-10A-01D-A35B-08 g.chrX:41012243_41012246delAATC c.1806_1809delAATC c.(1804-1809)ttaatcfs p.LI602fs PCPG 23 41045776 41045776 + Nonsense_Mutation SNP C C T TCGA-QR-A70U-01A-11D-A35D-08 TCGA-QR-A70U-10A-01D-A35B-08 g.chrX:41045776C>T c.3565C>T c.(3565-3567)Caa>Taa p.Q1189* PCPG 23 41069761 41069761 + Splice_Site SNP G G A TCGA-QR-A70U-01A-11D-A35D-08 TCGA-QR-A70U-10A-01D-A35B-08 g.chrX:41069761G>A c.e33-1 PRAD 23 40988337 40988337 + Nonsense_Mutation SNP G G T TCGA-ZG-A9LU-01A-11D-A41K-08 TCGA-ZG-A9LU-10A-01D-A41N-08 g.chrX:40988337G>T c.181G>T c.(181-183)Gaa>Taa p.E61* PRAD 23 40999970 40999970 + Missense_Mutation SNP A A G TCGA-HC-8257-01A-11D-2260-08 TCGA-HC-8257-10A-01D-2260-08 g.chrX:40999970A>G c.716A>G c.(715-717)gAt>gGt p.D239G PRAD 23 41000651 41000651 + Silent SNP G G A TCGA-EJ-5517-01A-01D-1576-08 TCGA-EJ-5517-10A-01D-1577-08 g.chrX:41000651G>A c.1128G>A c.(1126-1128)gaG>gaA p.E376E PRAD 23 41029390 41029390 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chrX:41029390G>A c.2779G>A c.(2779-2781)Gta>Ata p.V927I PRAD 23 41075904 41075904 + Splice_Site SNP C C T TCGA-V1-A9ZG-01A-11D-A41K-08 TCGA-V1-A9ZG-10A-01D-A41N-08 g.chrX:41075904C>T c.6084C>T c.(6082-6084)ccC>ccT p.P2028P PRAD 23 41082490 41082490 + Missense_Mutation SNP C C T TCGA-YL-A8SL-01B-21D-A377-08 TCGA-YL-A8SL-10A-01D-A37A-08 g.chrX:41082490C>T c.6586C>T c.(6586-6588)Ctt>Ttt p.L2196F READ 23 40996156 40996156 + Missense_Mutation SNP A A C TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chrX:40996156A>C c.535A>C c.(535-537)Aat>Cat p.N179H READ 23 41007672 41007672 + Silent SNP G G A TCGA-AG-A026-01A-32W-A096-10 TCGA-AG-A026-10A-01W-A096-10 g.chrX:41007672G>A c.1470G>A c.(1468-1470)ctG>ctA p.L490L READ 23 41084340 41084340 + Missense_Mutation SNP G G T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chrX:41084340G>T c.7011G>T c.(7009-7011)ttG>ttT p.L2337F SKCM 23 40982966 40982966 + Nonsense_Mutation SNP C C T TCGA-EE-A3J7-06A-11D-A20D-08 TCGA-EE-A3J7-10A-01D-A20D-08 g.chrX:40982966C>T c.85C>T c.(85-87)Caa>Taa p.Q29* SKCM 23 40982969 40982969 + Nonsense_Mutation SNP C C T TCGA-ER-A198-06A-11D-A196-08 TCGA-ER-A198-10A-01D-A198-08 g.chrX:40982969C>T c.88C>T c.(88-90)Cag>Tag p.Q30* SKCM 23 41000634 41000634 + Nonsense_Mutation SNP C C T TCGA-D9-A148-06A-11D-A19A-08 TCGA-D9-A148-10A-01D-A19A-08 g.chrX:41000634C>T c.1111C>T c.(1111-1113)Cga>Tga p.R371* SKCM 23 41007791 41007791 + Missense_Mutation SNP G G A TCGA-EE-A3AF-06A-11D-A196-08 TCGA-EE-A3AF-10A-01D-A198-08 g.chrX:41007791G>A c.1589G>A c.(1588-1590)aGt>aAt p.S530N SKCM 23 41010280 41010283 + Frame_Shift_Del DEL GTTT GTTT - TCGA-ER-A2NH-06A-11D-A196-08 TCGA-ER-A2NH-10A-01D-A198-08 g.chrX:41010280_41010283delGTTT c.1733_1736delGTTT c.(1732-1737)agtttgfs p.SL578fs SKCM 23 41029282 41029282 + Nonsense_Mutation SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chrX:41029282C>T c.2671C>T c.(2671-2673)Cga>Tga p.R891* SKCM 23 41029487 41029487 + Splice_Site SNP C C T TCGA-EE-A2MF-06A-11D-A21A-08 TCGA-EE-A2MF-10B-01D-A21A-08 g.chrX:41029487C>T c.2876C>T c.(2875-2877)tCg>tTg p.S959L SKCM 23 41043842 41043842 + Silent SNP T T C TCGA-EB-A5UL-06A-11D-A30X-08 TCGA-EB-A5UL-10A-01D-A30X-08 g.chrX:41043842T>C c.3472T>C c.(3472-3474)Ttg>Ctg p.L1158L SKCM 23 41043859 41043859 + Silent SNP C C T TCGA-D3-A51G-06A-11D-A25O-08 TCGA-D3-A51G-10A-01D-A25O-08 g.chrX:41043859C>T c.3489C>T c.(3487-3489)ggC>ggT p.G1163G SKCM 23 41045827 41045827 + Missense_Mutation SNP C C T TCGA-D3-A51G-06A-11D-A25O-08 TCGA-D3-A51G-10A-01D-A25O-08 g.chrX:41045827C>T c.3616C>T c.(3616-3618)Cct>Tct p.P1206S SKCM 23 41048638 41048638 + Missense_Mutation SNP T T C TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chrX:41048638T>C c.3887T>C c.(3886-3888)tTt>tCt p.F1296S SKCM 23 41055511 41055511 + Missense_Mutation SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chrX:41055511C>T c.3985C>T c.(3985-3987)Cgt>Tgt p.R1329C SKCM 23 41055511 41055511 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chrX:41055511C>T c.3985C>T c.(3985-3987)Cgt>Tgt p.R1329C SKCM 23 41055568 41055568 + Missense_Mutation SNP C C G TCGA-ER-A19P-06A-11D-A196-08 TCGA-ER-A19P-10A-01D-A198-08 g.chrX:41055568C>G c.4042C>G c.(4042-4044)Cgg>Ggg p.R1348G SKCM 23 41055614 41055614 + Splice_Site SNP T T G TCGA-FS-A1Z0-06A-11D-A197-08 TCGA-FS-A1Z0-10A-01D-A199-08 g.chrX:41055614T>G c.e27+2 SKCM 23 41057871 41057871 + Missense_Mutation SNP G G A TCGA-FS-A1Z0-06A-11D-A197-08 TCGA-FS-A1Z0-10A-01D-A199-08 g.chrX:41057871G>A c.4471G>A c.(4471-4473)Gtc>Atc p.V1491I SKCM 23 41069763 41069763 + Splice_Site SNP C C T TCGA-ER-A42L-06A-11D-A24R-08 TCGA-ER-A42L-10A-01D-A24R-08 g.chrX:41069763C>T c.5017C>T c.(5017-5019)Ctt>Ttt p.L1673F SKCM 23 41069821 41069821 + Missense_Mutation SNP C C T TCGA-DA-A1HV-06A-21D-A196-08 TCGA-DA-A1HV-10A-01D-A198-08 g.chrX:41069821C>T c.5075C>T c.(5074-5076)tCa>tTa p.S1692L SKCM 23 41069821 41069821 + Missense_Mutation SNP C C T TCGA-FS-A4F5-06A-11D-A25O-08 TCGA-FS-A4F5-10B-01D-A25O-08 g.chrX:41069821C>T c.5075C>T c.(5074-5076)tCa>tTa p.S1692L SKCM 23 41075159 41075159 + Missense_Mutation SNP C C T TCGA-FS-A1ZK-06A-11D-A197-08 TCGA-FS-A1ZK-10A-01D-A199-08 g.chrX:41075159C>T c.5339C>T c.(5338-5340)aCc>aTc p.T1780I SKCM 23 41075484 41075484 + Silent SNP T T C TCGA-D3-A2JO-06A-11D-A196-08 TCGA-D3-A2JO-10A-01D-A198-08 g.chrX:41075484T>C c.5664T>C c.(5662-5664)aaT>aaC p.N1888N SKCM 23 41084153 41084153 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chrX:41084153C>T c.6910C>T c.(6910-6912)Cgt>Tgt p.R2304C SKCM 23 41088904 41088904 + Missense_Mutation SNP C C T TCGA-D3-A3C7-06A-11D-A196-08 TCGA-D3-A3C7-10A-01D-A198-08 g.chrX:41088904C>T c.7303C>T c.(7303-7305)Cct>Tct p.P2435S

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation ALL-US X 41000486 41000492 deletion of <=200bp CTTGAAA - intron_variant AML-US X 41077773 41077773 insertion of <=200bp - GGCCT frameshift_variant I2120GL? BLCA-CN X 41007706 41007706 single base substitution G A missense_variant V502M 1504G>A BLCA-CN X 41025382 41025382 single base substitution A C missense_variant N748T 2243A>C BLCA-CN X 41025382 41025382 single base substitution A C upstream_gene_variant BLCA-CN X 41029818 41029818 single base substitution T C downstream_gene_variant BLCA-CN X 41029818 41029818 single base substitution T C synonymous_variant G991G 2973T>C BLCA-CN X 41077834 41077834 single base substitution C T missense_variant P2140L 6419C>T BLCA-US X 41010204 41010204 single base substitution G C missense_variant D553H 1657G>C BLCA-US X 41047370 41047370 insertion of <=200bp - GT downstream_gene_variant BLCA-US X 41047370 41047370 insertion of <=200bp - GT frameshift_variant K1270K? BLCA-US X 41047370 41047370 insertion of <=200bp - GT splice_region_variant BLCA-US X 41075732 41075732 single base substitution A G missense_variant E1971G 5912A>G BLCA-US X 41077663 41077663 single base substitution A T missense_variant N2083I 6248A>T BOCA-FR X 41057868 41057868 insertion of <=200bp - T downstream_gene_variant BOCA-FR X 41057868 41057868 insertion of <=200bp - T frameshift_variant P1490S? BRCA-EU X 40940743 40940743 single base substitution C G upstream_gene_variant BRCA-EU X 40941568 40941568 single base substitution T C upstream_gene_variant BRCA-EU X 40942377 40942377 single base substitution G A upstream_gene_variant BRCA-EU X 40942406 40942406 single base substitution A G upstream_gene_variant BRCA-EU X 40942608 40942608 single base substitution C G upstream_gene_variant BRCA-EU X 40943178 40943178 single base substitution C G upstream_gene_variant BRCA-EU X 40943263 40943263 single base substitution T C upstream_gene_variant BRCA-EU X 40943318 40943318 single base substitution C T upstream_gene_variant BRCA-EU X 40944197 40944197 single base substitution G C upstream_gene_variant BRCA-EU X 40946673 40946673 single base substitution G C intron_variant BRCA-EU X 40947551 40947551 single base substitution T G intron_variant BRCA-EU X 40948916 40948916 single base substitution C T intron_variant BRCA-EU X 40949919 40949919 deletion of <=200bp T - intron_variant BRCA-EU X 40950621 40950621 single base substitution G A intron_variant BRCA-EU X 40952009 40952009 single base substitution C G intron_variant BRCA-EU X 40952032 40952032 single base substitution G A intron_variant BRCA-EU X 40952661 40952661 single base substitution G A intron_variant BRCA-EU X 40953116 40953116 single base substitution C G intron_variant BRCA-EU X 40954081 40954081 single base substitution C T intron_variant BRCA-EU X 40954899 40954899 single base substitution G A intron_variant BRCA-EU X 40955461 40955461 single base substitution C T intron_variant BRCA-EU X 40955648 40955648 single base substitution A G intron_variant BRCA-EU X 40956547 40956547 single base substitution G C intron_variant BRCA-EU X 40957096 40957096 single base substitution G C intron_variant BRCA-EU X 40957736 40957736 single base substitution C T intron_variant BRCA-EU X 40960072 40960072 single base substitution G A intron_variant BRCA-EU X 40961293 40961293 single base substitution G A intron_variant BRCA-EU X 40962608 40962608 single base substitution G T intron_variant BRCA-EU X 40964166 40964166 single base substitution G A intron_variant BRCA-EU X 40964408 40964408 single base substitution C T intron_variant BRCA-EU X 40965690 40965690 single base substitution A C intron_variant BRCA-EU X 40966939 40966939 single base substitution C T intron_variant BRCA-EU X 40966961 40966961 deletion of <=200bp T - intron_variant BRCA-EU X 40967159 40967159 single base substitution C T intron_variant BRCA-EU X 40969568 40969568 single base substitution A G intron_variant BRCA-EU X 40970364 40970364 single base substitution G A intron_variant BRCA-EU X 40971284 40971284 single base substitution G C intron_variant BRCA-EU X 40974968 40974968 single base substitution C T intron_variant BRCA-EU X 40975017 40975017 deletion of <=200bp T - intron_variant BRCA-EU X 40975364 40975364 single base substitution T C intron_variant BRCA-EU X 40977055 40977055 single base substitution G A intron_variant BRCA-EU X 40977863 40977863 single base substitution A C intron_variant BRCA-EU X 40978385 40978385 single base substitution G A intron_variant BRCA-EU X 40979937 40979937 single base substitution G C intron_variant BRCA-EU X 40980398 40980398 single base substitution G T intron_variant BRCA-EU X 40980752 40980752 single base substitution G A intron_variant BRCA-EU X 40981345 40981345 deletion of <=200bp G - intron_variant BRCA-EU X 40981654 40981654 single base substitution G C intron_variant BRCA-EU X 40983272 40983272 single base substitution G A intron_variant BRCA-EU X 40983530 40983530 single base substitution C G intron_variant BRCA-EU X 40984986 40984986 single base substitution C T intron_variant BRCA-EU X 40988413 40988413 single base substitution A G intron_variant BRCA-EU X 40989101 40989106 deletion of <=200bp GCACTT - intron_variant BRCA-EU X 40992153 40992153 deletion of <=200bp T - intron_variant BRCA-EU X 40993020 40993020 single base substitution G T intron_variant BRCA-EU X 40993119 40993119 single base substitution C G intron_variant BRCA-EU X 40993337 40993337 deletion of <=200bp T - intron_variant BRCA-EU X 40994074 40994074 deletion of <=200bp G - frameshift_variant W140 BRCA-EU X 40995495 40995495 single base substitution C T intron_variant BRCA-EU X 40995598 40995598 single base substitution G C intron_variant BRCA-EU X 40996235 40996235 single base substitution A G missense_variant D205G 614A>G BRCA-EU X 40996452 40996452 single base substitution A G intron_variant BRCA-EU X 40998363 40998363 single base substitution G T intron_variant BRCA-EU X 40998952 40998952 single base substitution C T intron_variant BRCA-EU X 40999465 40999465 single base substitution T G intron_variant BRCA-EU X 40999825 40999825 single base substitution C T intron_variant BRCA-EU X 41000507 41000507 single base substitution G A intron_variant BRCA-EU X 41001416 41001416 single base substitution G C intron_variant BRCA-EU X 41001437 41001437 single base substitution G A intron_variant BRCA-EU X 41003850 41003850 single base substitution C G missense_variant Q464E 1390C>G BRCA-EU X 41005493 41005493 deletion of <=200bp C - intron_variant BRCA-EU X 41007201 41007201 single base substitution C T intron_variant BRCA-EU X 41007311 41007311 single base substitution C G intron_variant BRCA-EU X 41007652 41007652 single base substitution C T missense_variant R484C 1450C>T BRCA-EU X 41007950 41007950 deletion of <=200bp T - intron_variant BRCA-EU X 41008888 41008888 single base substitution G C intron_variant BRCA-EU X 41009521 41009521 single base substitution G C intron_variant BRCA-EU X 41011146 41011146 single base substitution A G intron_variant BRCA-EU X 41011368 41011368 single base substitution A C intron_variant BRCA-EU X 41012122 41012122 single base substitution G C intron_variant BRCA-EU X 41012434 41012434 single base substitution G C intron_variant BRCA-EU X 41012649 41012649 single base substitution G A intron_variant BRCA-EU X 41012683 41012683 single base substitution G A intron_variant BRCA-EU X 41015171 41015171 single base substitution G C intron_variant BRCA-EU X 41017022 41017022 single base substitution C T intron_variant BRCA-EU X 41017597 41017597 single base substitution C G intron_variant BRCA-EU X 41018509 41018509 single base substitution G T intron_variant BRCA-EU X 41018792 41018792 insertion of <=200bp - T intron_variant BRCA-EU X 41019083 41019083 single base substitution C T intron_variant BRCA-EU X 41019385 41019385 single base substitution A G intron_variant BRCA-EU X 41019500 41019500 single base substitution G C intron_variant BRCA-EU X 41020930 41020930 single base substitution T A intron_variant BRCA-EU X 41024986 41024986 single base substitution G C intron_variant BRCA-EU X 41024986 41024986 single base substitution G C upstream_gene_variant BRCA-EU X 41027794 41027794 single base substitution C T downstream_gene_variant BRCA-EU X 41027794 41027794 single base substitution C T intron_variant BRCA-EU X 41027913 41027913 deletion of <=200bp T - downstream_gene_variant BRCA-EU X 41027913 41027913 deletion of <=200bp T - intron_variant BRCA-EU X 41028154 41028154 single base substitution A T downstream_gene_variant BRCA-EU X 41028154 41028154 single base substitution A T intron_variant BRCA-EU X 41028758 41028758 single base substitution A T downstream_gene_variant BRCA-EU X 41028758 41028758 single base substitution A T intron_variant BRCA-EU X 41029235 41029235 deletion of <=200bp T - downstream_gene_variant BRCA-EU X 41029235 41029235 deletion of <=200bp T - intron_variant BRCA-EU X 41031092 41031092 single base substitution T G downstream_gene_variant BRCA-EU X 41031092 41031092 single base substitution T G missense_variant I1010R 3029T>G BRCA-EU X 41031667 41031667 single base substitution C T downstream_gene_variant BRCA-EU X 41031667 41031667 single base substitution C T intron_variant BRCA-EU X 41032041 41032041 deletion of <=200bp T - downstream_gene_variant BRCA-EU X 41032041 41032041 deletion of <=200bp T - intron_variant BRCA-EU X 41033337 41033337 single base substitution C A intron_variant BRCA-EU X 41033954 41033954 single base substitution G A intron_variant BRCA-EU X 41035409 41035409 single base substitution C T intron_variant BRCA-EU X 41036531 41036531 single base substitution T C intron_variant BRCA-EU X 41037092 41037092 single base substitution C A intron_variant BRCA-EU X 41037099 41037099 single base substitution A C intron_variant BRCA-EU X 41037943 41037943 single base substitution G A intron_variant BRCA-EU X 41041353 41041353 single base substitution C T intron_variant BRCA-EU X 41041353 41041353 single base substitution C T upstream_gene_variant BRCA-EU X 41041817 41041817 single base substitution G A intron_variant BRCA-EU X 41041817 41041817 single base substitution G A upstream_gene_variant BRCA-EU X 41043648 41043651 deletion of <=200bp AGGT - frameshift_variant EV1094 BRCA-EU X 41043648 41043651 deletion of <=200bp AGGT - splice_acceptor_variant BRCA-EU X 41043648 41043651 deletion of <=200bp AGGT - upstream_gene_variant BRCA-EU X 41044178 41044178 single base substitution C G downstream_gene_variant BRCA-EU X 41044178 41044178 single base substitution C G intron_variant BRCA-EU X 41044178 41044178 single base substitution C G upstream_gene_variant BRCA-EU X 41044347 41044347 single base substitution C A downstream_gene_variant BRCA-EU X 41044347 41044347 single base substitution C A intron_variant BRCA-EU X 41044347 41044347 single base substitution C A upstream_gene_variant BRCA-EU X 41046875 41046875 single base substitution T C downstream_gene_variant BRCA-EU X 41046875 41046875 single base substitution T C intron_variant BRCA-EU X 41046875 41046875 single base substitution T C upstream_gene_variant BRCA-EU X 41051876 41051876 single base substitution G T downstream_gene_variant BRCA-EU X 41051876 41051876 single base substitution G T intron_variant BRCA-EU X 41051876 41051876 single base substitution G T upstream_gene_variant BRCA-EU X 41052181 41052181 single base substitution G A downstream_gene_variant BRCA-EU X 41052181 41052181 single base substitution G A intron_variant BRCA-EU X 41052181 41052181 single base substitution G A upstream_gene_variant BRCA-EU X 41053637 41053637 single base substitution G A downstream_gene_variant BRCA-EU X 41053637 41053637 single base substitution G A intron_variant BRCA-EU X 41053637 41053637 single base substitution G A upstream_gene_variant BRCA-EU X 41054300 41054300 deletion of <=200bp T - intron_variant BRCA-EU X 41054300 41054300 deletion of <=200bp T - upstream_gene_variant BRCA-EU X 41054997 41054997 single base substitution C T intron_variant BRCA-EU X 41054997 41054997 single base substitution C T upstream_gene_variant BRCA-EU X 41055173 41055173 single base substitution C A exon_variant BRCA-EU X 41055173 41055173 single base substitution C A intron_variant BRCA-EU X 41055902 41055902 single base substitution C A 3_prime_UTR_variant BRCA-EU X 41055902 41055902 single base substitution C A missense_variant L1382I 4144C>A BRCA-EU X 41056867 41056867 single base substitution G C intron_variant BRCA-EU X 41057586 41057586 single base substitution C T intron_variant BRCA-EU X 41057722 41057722 deletion of <=200bp T - intron_variant BRCA-EU X 41057892 41057892 single base substitution A T downstream_gene_variant BRCA-EU X 41057892 41057892 single base substitution A T missense_variant I1498F 4492A>T BRCA-EU X 41057948 41057951 deletion of <=200bp CAAA - downstream_gene_variant BRCA-EU X 41057948 41057951 deletion of <=200bp CAAA - frameshift_variant LK1516 BRCA-EU X 41058934 41058934 single base substitution G A downstream_gene_variant BRCA-EU X 41058934 41058934 single base substitution G A intron_variant BRCA-EU X 41059907 41059907 single base substitution A G downstream_gene_variant BRCA-EU X 41059907 41059907 single base substitution A G intron_variant BRCA-EU X 41059907 41059907 single base substitution A G upstream_gene_variant BRCA-EU X 41059984 41059984 single base substitution G A downstream_gene_variant BRCA-EU X 41059984 41059984 single base substitution G A intron_variant BRCA-EU X 41059984 41059984 single base substitution G A upstream_gene_variant BRCA-EU X 41060501 41060501 single base substitution G A downstream_gene_variant BRCA-EU X 41060501 41060501 single base substitution G A missense_variant D1598N 4792G>A BRCA-EU X 41060501 41060501 single base substitution G A upstream_gene_variant BRCA-EU X 41060866 41060866 single base substitution A G downstream_gene_variant BRCA-EU X 41060866 41060866 single base substitution A G intron_variant BRCA-EU X 41060866 41060866 single base substitution A G upstream_gene_variant BRCA-EU X 41061462 41061462 single base substitution G C downstream_gene_variant BRCA-EU X 41061462 41061462 single base substitution G C intron_variant BRCA-EU X 41061462 41061462 single base substitution G C upstream_gene_variant BRCA-EU X 41061716 41061716 single base substitution G A downstream_gene_variant BRCA-EU X 41061716 41061716 single base substitution G A intron_variant BRCA-EU X 41061716 41061716 single base substitution G A upstream_gene_variant BRCA-EU X 41061783 41061783 single base substitution G C downstream_gene_variant BRCA-EU X 41061783 41061783 single base substitution G C intron_variant BRCA-EU X 41061783 41061783 single base substitution G C upstream_gene_variant BRCA-EU X 41061944 41061944 single base substitution A G downstream_gene_variant BRCA-EU X 41061944 41061944 single base substitution A G intron_variant BRCA-EU X 41061944 41061944 single base substitution A G upstream_gene_variant BRCA-EU X 41063051 41063051 single base substitution A G intron_variant BRCA-EU X 41063051 41063051 single base substitution A G upstream_gene_variant BRCA-EU X 41063768 41063768 single base substitution A G intron_variant BRCA-EU X 41063768 41063768 single base substitution A G upstream_gene_variant BRCA-EU X 41064240 41064240 single base substitution T C intron_variant BRCA-EU X 41064240 41064240 single base substitution T C upstream_gene_variant BRCA-EU X 41065712 41065712 deletion of <=200bp T - intron_variant BRCA-EU X 41066309 41066309 single base substitution G C intron_variant BRCA-EU X 41066538 41066538 single base substitution G A intron_variant BRCA-EU X 41066958 41066958 single base substitution C T intron_variant BRCA-EU X 41075672 41075672 insertion of <=200bp - T frameshift_variant L1951L? BRCA-EU X 41076923 41076923 single base substitution G C intron_variant BRCA-EU X 41077173 41077173 single base substitution G C intron_variant BRCA-EU X 41079709 41079709 single base substitution T G intron_variant BRCA-EU X 41080243 41080243 single base substitution G A intron_variant BRCA-EU X 41080515 41080515 single base substitution A T intron_variant BRCA-EU X 41081783 41081783 single base substitution T C intron_variant BRCA-EU X 41082124 41082124 single base substitution T C intron_variant BRCA-EU X 41082879 41082879 single base substitution G A intron_variant BRCA-EU X 41085290 41085290 single base substitution G C intron_variant BRCA-EU X 41085290 41085290 single base substitution G C upstream_gene_variant BRCA-EU X 41085302 41085302 deletion of <=200bp T - intron_variant BRCA-EU X 41085302 41085302 deletion of <=200bp T - upstream_gene_variant BRCA-EU X 41085553 41085553 deletion of <=200bp T - intron_variant BRCA-EU X 41085553 41085553 deletion of <=200bp T - upstream_gene_variant BRCA-EU X 41087270 41087270 single base substitution T C intron_variant BRCA-EU X 41087270 41087270 single base substitution T C upstream_gene_variant BRCA-EU X 41088555 41088555 single base substitution G C exon_variant BRCA-EU X 41088555 41088555 single base substitution G C missense_variant D2371H 7111G>C BRCA-EU X 41089548 41089548 single base substitution T G downstream_gene_variant BRCA-EU X 41089548 41089548 single base substitution T G intron_variant BRCA-EU X 41091075 41091075 single base substitution T G downstream_gene_variant BRCA-EU X 41091075 41091075 single base substitution T G intron_variant BRCA-EU X 41092121 41092121 single base substitution C A 3_prime_UTR_variant BRCA-EU X 41092121 41092121 single base substitution C A downstream_gene_variant BRCA-EU X 41092628 41092628 single base substitution C A 3_prime_UTR_variant BRCA-EU X 41092628 41092628 single base substitution C A downstream_gene_variant BRCA-EU X 41093313 41093314 deletion of <=200bp TA - 3_prime_UTR_variant BRCA-EU X 41093313 41093314 deletion of <=200bp TA - downstream_gene_variant BRCA-EU X 41093318 41093318 single base substitution G C 3_prime_UTR_variant BRCA-EU X 41093318 41093318 single base substitution G C downstream_gene_variant BRCA-EU X 41094772 41094772 single base substitution G A 3_prime_UTR_variant BRCA-EU X 41094772 41094772 single base substitution G A downstream_gene_variant BRCA-EU X 41094931 41094931 single base substitution T C 3_prime_UTR_variant BRCA-EU X 41094931 41094931 single base substitution T C downstream_gene_variant BRCA-EU X 41096108 41096108 single base substitution G C downstream_gene_variant BRCA-EU X 41097091 41097091 single base substitution G C downstream_gene_variant BRCA-EU X 41097512 41097512 single base substitution C G downstream_gene_variant BRCA-EU X 41097693 41097693 deletion of <=200bp T - downstream_gene_variant BRCA-EU X 41097749 41097749 single base substitution T G downstream_gene_variant BRCA-EU X 41098267 41098267 single base substitution T G downstream_gene_variant BRCA-EU X 41098379 41098379 single base substitution T C downstream_gene_variant BRCA-EU X 41098621 41098621 single base substitution T G downstream_gene_variant BRCA-EU X 41098856 41098856 single base substitution C T downstream_gene_variant BRCA-EU X 41099886 41099886 single base substitution A G downstream_gene_variant BRCA-FR X 40942377 40942377 single base substitution G A upstream_gene_variant BRCA-FR X 40943178 40943178 single base substitution C G upstream_gene_variant BRCA-FR X 40947551 40947551 single base substitution T G intron_variant BRCA-FR X 40953116 40953116 single base substitution C G intron_variant BRCA-FR X 40954899 40954899 single base substitution G A intron_variant BRCA-FR X 40967159 40967159 single base substitution C T intron_variant BRCA-FR X 40971284 40971284 single base substitution G C intron_variant BRCA-FR X 40974393 40974393 single base substitution G A intron_variant BRCA-FR X 40979937 40979937 single base substitution G C intron_variant BRCA-FR X 40981654 40981654 single base substitution G C intron_variant BRCA-FR X 40983530 40983530 single base substitution C G intron_variant BRCA-FR X 40993119 40993119 single base substitution C G intron_variant BRCA-FR X 40995598 40995598 single base substitution G C intron_variant BRCA-FR X 40998952 40998952 single base substitution C T intron_variant BRCA-FR X 41009521 41009521 single base substitution G C intron_variant BRCA-FR X 41012122 41012122 single base substitution G C intron_variant BRCA-FR X 41021888 41021888 single base substitution G A intron_variant BRCA-FR X 41021888 41021888 single base substitution G A upstream_gene_variant BRCA-FR X 41052181 41052181 single base substitution G A downstream_gene_variant BRCA-FR X 41052181 41052181 single base substitution G A intron_variant BRCA-FR X 41052181 41052181 single base substitution G A upstream_gene_variant BRCA-FR X 41053637 41053637 single base substitution G A downstream_gene_variant BRCA-FR X 41053637 41053637 single base substitution G A intron_variant BRCA-FR X 41053637 41053637 single base substitution G A upstream_gene_variant BRCA-FR X 41053756 41053756 single base substitution G A downstream_gene_variant BRCA-FR X 41053756 41053756 single base substitution G A intron_variant BRCA-FR X 41053756 41053756 single base substitution G A upstream_gene_variant BRCA-FR X 41056867 41056867 single base substitution G C intron_variant BRCA-FR X 41060501 41060501 single base substitution G A downstream_gene_variant BRCA-FR X 41060501 41060501 single base substitution G A missense_variant D1598N 4792G>A BRCA-FR X 41060501 41060501 single base substitution G A upstream_gene_variant BRCA-FR X 41076923 41076923 single base substitution G C intron_variant BRCA-FR X 41091570 41091570 single base substitution C T downstream_gene_variant BRCA-FR X 41091570 41091570 single base substitution C T intron_variant BRCA-FR X 41094168 41094168 single base substitution G A 3_prime_UTR_variant BRCA-FR X 41094168 41094168 single base substitution G A downstream_gene_variant BRCA-FR X 41098856 41098856 single base substitution C T downstream_gene_variant BRCA-KR X 41029847 41029847 single base substitution A G downstream_gene_variant BRCA-KR X 41029847 41029847 single base substitution A G missense_variant E1001G 3002A>G BRCA-UK X 40955461 40955461 single base substitution C T intron_variant BRCA-UK X 40961293 40961293 single base substitution G A intron_variant BRCA-UK X 40969568 40969568 single base substitution A G intron_variant BRCA-UK X 40980398 40980398 single base substitution G T intron_variant BRCA-UK X 41001416 41001416 single base substitution G C intron_variant BRCA-UK X 41025335 41025335 single base substitution A G synonymous_variant L732L 2196A>G BRCA-UK X 41025335 41025335 single base substitution A G upstream_gene_variant BRCA-UK X 41039743 41039743 single base substitution G A intron_variant BRCA-UK X 41039743 41039743 single base substitution G A upstream_gene_variant BRCA-UK X 41041126 41041126 single base substitution C G intron_variant BRCA-UK X 41041126 41041126 single base substitution C G upstream_gene_variant BRCA-UK X 41073912 41073912 single base substitution G T downstream_gene_variant BRCA-UK X 41073912 41073912 single base substitution G T missense_variant D1761Y 5281G>T BRCA-UK X 41077173 41077173 single base substitution G C intron_variant BRCA-UK X 41077650 41077650 single base substitution C T missense_variant R2079C 6235C>T BRCA-UK X 41077683 41077683 single base substitution C G missense_variant H2090D 6268C>G BRCA-UK X 41079578 41079578 single base substitution C T intron_variant BRCA-UK X 41094772 41094772 single base substitution G A 3_prime_UTR_variant BRCA-UK X 41094772 41094772 single base substitution G A downstream_gene_variant BRCA-UK X 41096674 41096674 single base substitution C G downstream_gene_variant BRCA-US X 40990740 40990741 deletion of <=200bp AG - frameshift_variant KG91 BRCA-US X 40990750 40990750 single base substitution G C missense_variant E95Q 283G>C BRCA-US X 41007789 41007789 single base substitution C T synonymous_variant L529L 1587C>T BRCA-US X 41010191 41010191 single base substitution G T missense_variant K548N 1644G>T BRCA-US X 41012240 41012240 single base substitution C T synonymous_variant D601D 1803C>T BRCA-US X 41025364 41025364 single base substitution G A missense_variant R742Q 2225G>A BRCA-US X 41025364 41025364 single base substitution G A upstream_gene_variant BRCA-US X 41025387 41025387 single base substitution C T stop_gained R750* 2248C>T BRCA-US X 41025387 41025387 single base substitution C T upstream_gene_variant BRCA-US X 41043849 41043849 single base substitution C G exon_variant BRCA-US X 41043849 41043849 single base substitution C G missense_variant T1160S 3479C>G BRCA-US X 41043849 41043849 single base substitution C G upstream_gene_variant BRCA-US X 41047365 41047365 single base substitution G C downstream_gene_variant BRCA-US X 41047365 41047365 single base substitution G C exon_variant BRCA-US X 41047365 41047365 single base substitution G C missense_variant E1269Q 3805G>C BRCA-US X 41048627 41048627 single base substitution G A downstream_gene_variant BRCA-US X 41048627 41048627 single base substitution G A exon_variant BRCA-US X 41048627 41048627 single base substitution G A missense_variant M1292I 3876G>A BRCA-US X 41048632 41048632 insertion of <=200bp - A downstream_gene_variant BRCA-US X 41048632 41048632 insertion of <=200bp - A exon_variant BRCA-US X 41048632 41048632 insertion of <=200bp - A frameshift_variant L1294Y? BRCA-US X 41048645 41048645 single base substitution G C downstream_gene_variant BRCA-US X 41048645 41048645 single base substitution G C exon_variant BRCA-US X 41048645 41048645 single base substitution G C missense_variant L1298F 3894G>C BRCA-US X 41055854 41055855 deletion of <=200bp AG - 3_prime_UTR_variant BRCA-US X 41055854 41055855 deletion of <=200bp AG - frameshift_variant R1366 BRCA-US X 41056704 41056704 single base substitution C T 3_prime_UTR_variant BRCA-US X 41056704 41056704 single base substitution C T stop_gained Q1441* 4321C>T BRCA-US X 41073963 41073963 single base substitution G A downstream_gene_variant BRCA-US X 41073963 41073963 single base substitution G A splice_donor_variant BRCA-US X 41075185 41075185 single base substitution T C synonymous_variant L1789L 5365T>C BRCA-US X 41075313 41075313 single base substitution T G synonymous_variant G1831G 5493T>G BRCA-US X 41075620 41075620 single base substitution A C missense_variant M1934L 5800A>C BRCA-US X 41075653 41075653 single base substitution T G missense_variant W1945G 5833T>G BRCA-US X 41076559 41076559 single base substitution C G missense_variant H2058D 6172C>G BRCA-US X 41082490 41082490 single base substitution C G missense_variant L2196V 6586C>G BRCA-US X 41084197 41084197 insertion of <=200bp - A frameshift_variant L2318L? BRCA-US X 41084197 41084197 insertion of <=200bp - A upstream_gene_variant BTCA-JP X 41012380 41012380 deletion of <=200bp T - intron_variant BTCA-JP X 41031233 41031233 single base substitution T A downstream_gene_variant BTCA-JP X 41031233 41031233 single base substitution T A intron_variant BTCA-JP X 41031234 41031234 single base substitution C G downstream_gene_variant BTCA-JP X 41031234 41031234 single base substitution C G intron_variant BTCA-JP X 41056716 41056716 insertion of <=200bp - A 3_prime_UTR_variant BTCA-JP X 41056716 41056716 insertion of <=200bp - A frameshift_variant K1445K? BTCA-JP X 41074064 41074064 single base substitution C T downstream_gene_variant BTCA-JP X 41074064 41074064 single base substitution C T intron_variant BTCA-JP X 41088849 41088849 single base substitution C T exon_variant BTCA-JP X 41088849 41088849 single base substitution C T synonymous_variant T2416T 7248C>T CESC-US X 40999952 40999952 single base substitution G A missense_variant G233E 698G>A CESC-US X 41029361 41029361 single base substitution G A downstream_gene_variant CESC-US X 41029361 41029361 single base substitution G A missense_variant R917Q 2750G>A CESC-US X 41043695 41043695 single base substitution G A exon_variant CESC-US X 41043695 41043695 single base substitution G A missense_variant D1109N 3325G>A CESC-US X 41043695 41043695 single base substitution G A upstream_gene_variant CESC-US X 41047349 41047349 insertion of <=200bp - TT downstream_gene_variant CESC-US X 41047349 41047349 insertion of <=200bp - TT exon_variant CESC-US X 41047349 41047349 insertion of <=200bp - TT frameshift_variant E1263D? CESC-US X 41055534 41055534 single base substitution C A exon_variant CESC-US X 41055534 41055534 single base substitution C A missense_variant F1336L 4008C>A CESC-US X 41055965 41055965 single base substitution G A 3_prime_UTR_variant CESC-US X 41055965 41055965 single base substitution G A missense_variant E1403K 4207G>A CESC-US X 41075524 41075524 single base substitution G A missense_variant D1902N 5704G>A CESC-US X 41077746 41077746 single base substitution G A missense_variant E2111K 6331G>A CESC-US X 41089034 41089034 insertion of <=200bp - A exon_variant CESC-US X 41089034 41089034 insertion of <=200bp - A frameshift_variant V2478D? CESC-US X 41089034 41089034 insertion of <=200bp - A splice_donor_variant CLLE-ES X 40951128 40951128 single base substitution A T intron_variant CLLE-ES X 40984971 40984976 multiple base substitution (>=2bp and <=200bp) TCGCGC TCTCTCGCGCGC intron_variant CLLE-ES X 41059324 41059324 single base substitution A T downstream_gene_variant CLLE-ES X 41059324 41059324 single base substitution A T intron_variant CLLE-ES X 41059324 41059324 single base substitution A T upstream_gene_variant CLLE-ES X 41075566 41075566 single base substitution A G missense_variant M1916V 5746A>G CLLE-ES X 41081920 41081920 single base substitution C T intron_variant CLLE-ES X 41099033 41099033 single base substitution T G downstream_gene_variant COAD-US X 40982912 40982912 single base substitution G A missense_variant G11R 31G>A COAD-US X 40988350 40988350 single base substitution C A missense_variant P65H 194C>A COAD-US X 40990737 40990737 single base substitution G T synonymous_variant P90P 270G>T COAD-US X 40996081 40996081 single base substitution C T missense_variant R154C 460C>T COAD-US X 41000437 41000437 single base substitution A C missense_variant N330T 989A>C COAD-US X 41010222 41010222 single base substitution C A missense_variant L559I 1675C>A COAD-US X 41022042 41022042 single base substitution G A splice_acceptor_variant COAD-US X 41022042 41022042 single base substitution G A upstream_gene_variant COAD-US X 41025392 41025392 single base substitution A C missense_variant E751D 2253A>C COAD-US X 41025392 41025392 single base substitution A C upstream_gene_variant COAD-US X 41029361 41029361 single base substitution G A downstream_gene_variant COAD-US X 41029361 41029361 single base substitution G A missense_variant R917Q 2750G>A COAD-US X 41055599 41055599 single base substitution T C 3_prime_UTR_variant COAD-US X 41055599 41055599 single base substitution T C missense_variant F1358S 4073T>C COAD-US X 41055978 41055978 single base substitution T G 3_prime_UTR_variant COAD-US X 41055978 41055978 single base substitution T G missense_variant L1407R 4220T>G COAD-US X 41057839 41057839 single base substitution A C downstream_gene_variant COAD-US X 41057839 41057839 single base substitution A C missense_variant N1480T 4439A>C COAD-US X 41064704 41064704 single base substitution G A exon_variant COAD-US X 41064704 41064704 single base substitution G A missense_variant R1658Q 4973G>A COAD-US X 41069809 41069809 single base substitution A C exon_variant COAD-US X 41069809 41069809 single base substitution A C missense_variant E1688A 5063A>C COAD-US X 41075373 41075373 single base substitution G T missense_variant E1851D 5553G>T COAD-US X 41075428 41075428 single base substitution G A missense_variant V1870I 5608G>A COAD-US X 41075506 41075506 single base substitution C T missense_variant R1896C 5686C>T COAD-US X 41075672 41075672 deletion of <=200bp T - frameshift_variant L1951 COAD-US X 41076578 41076578 single base substitution G A missense_variant R2064H 6191G>A COAD-US X 41077661 41077661 single base substitution G T missense_variant K2082N 6246G>T COAD-US X 41078483 41078483 single base substitution A T missense_variant L2188F 6564A>T COAD-US X 41082527 41082527 single base substitution T C missense_variant V2208A 6623T>C COAD-US X 41084097 41084097 single base substitution A G missense_variant Y2285C 6854A>G COAD-US X 41084097 41084097 single base substitution A G upstream_gene_variant COAD-US X 41088571 41088571 insertion of <=200bp - T exon_variant COAD-US X 41088571 41088571 insertion of <=200bp - T frameshift_variant S2376F? COAD-US X 41088663 41088663 single base substitution G A splice_donor_variant COAD-US X 41089035 41089035 deletion of <=200bp A - exon_variant COAD-US X 41089035 41089035 deletion of <=200bp A - frameshift_variant V2478 COAD-US X 41089035 41089035 deletion of <=200bp A - splice_region_variant COAD-US X 41091690 41091690 single base substitution G T downstream_gene_variant COAD-US X 41091690 41091690 single base substitution G T missense_variant M2526I 7578G>T COAD-US X 41091690 41091690 single base substitution G T missense_variant M2542I 7626G>T COCA-CN X 40990670 40990670 single base substitution T C intron_variant COCA-CN X 40994229 40994229 single base substitution A C intron_variant COCA-CN X 40996185 40996185 single base substitution T C synonymous_variant N188N 564T>C COCA-CN X 41000218 41000218 single base substitution G A splice_acceptor_variant COCA-CN X 41003860 41003860 single base substitution A G missense_variant H467R 1400A>G COCA-CN X 41025430 41025430 single base substitution A G missense_variant D764G 2291A>G COCA-CN X 41025430 41025430 single base substitution A G upstream_gene_variant COCA-CN X 41026929 41026929 single base substitution T G intron_variant COCA-CN X 41027281 41027281 single base substitution A G exon_variant COCA-CN X 41027281 41027281 single base substitution A G missense_variant I816V 2446A>G COCA-CN X 41043944 41043944 single base substitution T C exon_variant COCA-CN X 41043944 41043944 single base substitution T C intron_variant COCA-CN X 41043944 41043944 single base substitution T C upstream_gene_variant COCA-CN X 41045764 41045764 single base substitution T G downstream_gene_variant COCA-CN X 41045764 41045764 single base substitution T G splice_region_variant COCA-CN X 41045764 41045764 single base substitution T G upstream_gene_variant COCA-CN X 41048557 41048557 single base substitution T C downstream_gene_variant COCA-CN X 41048557 41048557 single base substitution T C intron_variant COCA-CN X 41048557 41048557 single base substitution T C splice_region_variant COCA-CN X 41057994 41057994 single base substitution G A downstream_gene_variant COCA-CN X 41057994 41057994 single base substitution G A missense_variant A1532T 4594G>A COCA-CN X 41089109 41089109 single base substitution T C exon_variant COCA-CN X 41089109 41089109 single base substitution T C intron_variant EOPC-DE X 40989440 40989440 single base substitution C A intron_variant EOPC-DE X 40995657 40995657 single base substitution G A intron_variant EOPC-DE X 41068231 41068231 single base substitution G T intron_variant ESCA-CN X 41003796 41003796 single base substitution G A missense_variant V446M 1336G>A ESCA-CN X 41007808 41007808 single base substitution C T synonymous_variant L536L 1606C>T ESCA-CN X 41010088 41010088 deletion of <=200bp T - intron_variant ESCA-CN X 41048617 41048617 single base substitution T A downstream_gene_variant ESCA-CN X 41048617 41048617 single base substitution T A exon_variant ESCA-CN X 41048617 41048617 single base substitution T A stop_gained L1289* 3866T>A ESCA-CN X 41055885 41055885 single base substitution T G 3_prime_UTR_variant ESCA-CN X 41055885 41055885 single base substitution T G missense_variant F1376C 4127T>G ESCA-CN X 41073730 41073730 single base substitution A T downstream_gene_variant ESCA-CN X 41073730 41073730 single base substitution A T intron_variant ESCA-CN X 41075106 41075106 single base substitution G T intron_variant ESCA-CN X 41092918 41092918 single base substitution G C 3_prime_UTR_variant ESCA-CN X 41092918 41092918 single base substitution G C downstream_gene_variant GBM-US X 41075424 41075424 single base substitution G A synonymous_variant V1868V 5604G>A GBM-US X 41075440 41075440 single base substitution C T stop_gained Q1874* 5620C>T GBM-US X 41075579 41075579 single base substitution G C missense_variant C1920S 5759G>C KIRC-US X 41025293 41025293 single base substitution C A missense_variant D718E 2154C>A KIRC-US X 41025293 41025293 single base substitution C A upstream_gene_variant KIRC-US X 41025335 41025335 single base substitution A G synonymous_variant L732L 2196A>G KIRC-US X 41025335 41025335 single base substitution A G upstream_gene_variant KIRC-US X 41047253 41047253 single base substitution A G downstream_gene_variant KIRC-US X 41047253 41047253 single base substitution A G synonymous_variant R1231R 3693A>G KIRC-US X 41047253 41047253 single base substitution A G upstream_gene_variant KIRC-US X 41077774 41077774 single base substitution T C missense_variant I2120T 6359T>C KIRC-US X 41088595 41088595 single base substitution C A exon_variant KIRC-US X 41088595 41088595 single base substitution C A missense_variant A2384E 7151C>A KIRC-US X 41091721 41091721 single base substitution C G downstream_gene_variant KIRC-US X 41091721 41091721 single base substitution C G missense_variant Q2537E 7609C>G KIRC-US X 41091721 41091721 single base substitution C G missense_variant Q2553E 7657C>G KIRP-US X 40999924 40999924 single base substitution C A missense_variant L224I 670C>A KIRP-US X 41022128 41022128 single base substitution T C splice_region_variant KIRP-US X 41022128 41022128 single base substitution T C upstream_gene_variant KIRP-US X 41043810 41043810 single base substitution C T exon_variant KIRP-US X 41043810 41043810 single base substitution C T missense_variant A1147V 3440C>T KIRP-US X 41043810 41043810 single base substitution C T upstream_gene_variant LAML-KR X 40990071 40990071 single base substitution C T intron_variant LAML-KR X 40993907 40993907 single base substitution T G intron_variant LAML-KR X 40993938 40993938 single base substitution G A intron_variant LAML-KR X 41071112 41071112 single base substitution G A downstream_gene_variant LAML-KR X 41071112 41071112 single base substitution G A intron_variant LAML-KR X 41071119 41071119 single base substitution C T downstream_gene_variant LAML-KR X 41071119 41071119 single base substitution C T intron_variant LAML-KR X 41071142 41071142 single base substitution T C downstream_gene_variant LAML-KR X 41071142 41071142 single base substitution T C intron_variant LAML-KR X 41071282 41071282 single base substitution G A downstream_gene_variant LAML-KR X 41071282 41071282 single base substitution G A intron_variant LAML-KR X 41071304 41071304 single base substitution C T downstream_gene_variant LAML-KR X 41071304 41071304 single base substitution C T intron_variant LAML-KR X 41071333 41071333 single base substitution G A downstream_gene_variant LAML-KR X 41071333 41071333 single base substitution G A intron_variant LAML-KR X 41071462 41071462 single base substitution G A downstream_gene_variant LAML-KR X 41071462 41071462 single base substitution G A intron_variant LAML-KR X 41073730 41073730 single base substitution A T downstream_gene_variant LAML-KR X 41073730 41073730 single base substitution A T intron_variant LAML-KR X 41073734 41073734 single base substitution A G downstream_gene_variant LAML-KR X 41073734 41073734 single base substitution A G intron_variant LAML-KR X 41099178 41099178 single base substitution C T downstream_gene_variant LAML-KR X 41099186 41099186 single base substitution A G downstream_gene_variant LAML-KR X 41099495 41099495 single base substitution C T downstream_gene_variant LAML-KR X 41099498 41099498 single base substitution G A downstream_gene_variant LAML-KR X 41099669 41099669 single base substitution C T downstream_gene_variant LGG-US X 41057788 41057788 single base substitution T C 3_prime_UTR_variant LGG-US X 41057788 41057788 single base substitution T C missense_variant I1463T 4388T>C LGG-US X 41075260 41075260 single base substitution G A missense_variant D1814N 5440G>A LGG-US X 41084138 41084138 single base substitution A G missense_variant T2299A 6895A>G LGG-US X 41084138 41084138 single base substitution A G upstream_gene_variant LGG-US X 41088882 41088884 deletion of <=200bp AAG - exon_variant LGG-US X 41088882 41088884 deletion of <=200bp AAG - inframe_deletion ER2427E LICA-CN X 41022108 41022108 single base substitution C T stop_gained Q655* 1963C>T LICA-CN X 41022108 41022108 single base substitution C T upstream_gene_variant LICA-CN X 41047312 41047312 single base substitution G T downstream_gene_variant LICA-CN X 41047312 41047312 single base substitution G T missense_variant C1251F 3752G>T LICA-CN X 41047312 41047312 single base substitution G T upstream_gene_variant LICA-CN X 41048645 41048645 single base substitution G C downstream_gene_variant LICA-CN X 41048645 41048645 single base substitution G C exon_variant LICA-CN X 41048645 41048645 single base substitution G C missense_variant L1298F 3894G>C LICA-CN X 41073842 41073842 single base substitution T C downstream_gene_variant LICA-CN X 41073842 41073842 single base substitution T C synonymous_variant F1737F 5211T>C LICA-CN X 41073957 41073957 single base substitution A T downstream_gene_variant LICA-CN X 41073957 41073957 single base substitution A T stop_gained K1776* 5326A>T LICA-FR X 40951994 40951994 insertion of <=200bp - A intron_variant LICA-FR X 41000584 41000599 deletion of <=200bp CACTGAATGAAGTTAA - frameshift_variant ALNEVN354 LICA-FR X 41002563 41002563 single base substitution A G missense_variant N394S 1181A>G LICA-FR X 41004775 41004775 single base substitution A G intron_variant LICA-FR X 41005517 41005517 single base substitution A G intron_variant LICA-FR X 41055929 41055929 single base substitution A G 3_prime_UTR_variant LICA-FR X 41055929 41055929 single base substitution A G missense_variant I1391V 4171A>G LICA-FR X 41068398 41068398 single base substitution A G intron_variant LICA-FR X 41090985 41090985 deletion of <=200bp A - downstream_gene_variant LICA-FR X 41090985 41090985 deletion of <=200bp A - intron_variant LICA-FR X 41091750 41091753 deletion of <=200bp ATCC - downstream_gene_variant LICA-FR X 41091750 41091753 deletion of <=200bp ATCC - frameshift_variant VS2546 LICA-FR X 41091750 41091753 deletion of <=200bp ATCC - frameshift_variant VS2562 LIHC-US X 41002598 41002598 single base substitution C G missense_variant Q406E 1216C>G LIHC-US X 41012219 41012219 single base substitution C T synonymous_variant P594P 1782C>T LIHC-US X 41069765 41069765 single base substitution T A exon_variant LIHC-US X 41069765 41069765 single base substitution T A synonymous_variant L1673L 5019T>A LIHC-US X 41088999 41088999 single base substitution A G exon_variant LIHC-US X 41088999 41088999 single base substitution A G synonymous_variant T2466T 7398A>G LINC-JP X 40943950 40943950 single base substitution G C upstream_gene_variant LINC-JP X 40953447 40953447 single base substitution G T intron_variant LINC-JP X 40958504 40958504 single base substitution G T intron_variant LINC-JP X 40964047 40964047 single base substitution A G intron_variant LINC-JP X 40979230 40979230 single base substitution G T intron_variant LINC-JP X 40990987 40990987 single base substitution A G intron_variant LINC-JP X 40996330 40996330 single base substitution C T intron_variant LINC-JP X 41003389 41003389 single base substitution A G intron_variant LINC-JP X 41008063 41008063 single base substitution G T intron_variant LINC-JP X 41020719 41020719 single base substitution A G intron_variant LINC-JP X 41024455 41024455 single base substitution A C intron_variant LINC-JP X 41024455 41024455 single base substitution A C upstream_gene_variant LINC-JP X 41025710 41025710 single base substitution G T intron_variant LINC-JP X 41025710 41025710 single base substitution G T upstream_gene_variant LINC-JP X 41031261 41031261 single base substitution A G downstream_gene_variant LINC-JP X 41031261 41031261 single base substitution A G intron_variant LINC-JP X 41031270 41031270 single base substitution A C downstream_gene_variant LINC-JP X 41031270 41031270 single base substitution A C intron_variant LINC-JP X 41031943 41031943 single base substitution C T downstream_gene_variant LINC-JP X 41031943 41031943 single base substitution C T intron_variant LINC-JP X 41032370 41032370 single base substitution T G downstream_gene_variant LINC-JP X 41032370 41032370 single base substitution T G intron_variant LINC-JP X 41043088 41043088 single base substitution C T intron_variant LINC-JP X 41043088 41043088 single base substitution C T upstream_gene_variant LINC-JP X 41043172 41043172 single base substitution A G intron_variant LINC-JP X 41043172 41043172 single base substitution A G upstream_gene_variant LINC-JP X 41044765 41044765 single base substitution A G downstream_gene_variant LINC-JP X 41044765 41044765 single base substitution A G intron_variant LINC-JP X 41044765 41044765 single base substitution A G upstream_gene_variant LINC-JP X 41045055 41045055 single base substitution A G downstream_gene_variant LINC-JP X 41045055 41045055 single base substitution A G intron_variant LINC-JP X 41045055 41045055 single base substitution A G upstream_gene_variant LINC-JP X 41047213 41047213 single base substitution A G downstream_gene_variant LINC-JP X 41047213 41047213 single base substitution A G intron_variant LINC-JP X 41047213 41047213 single base substitution A G upstream_gene_variant LINC-JP X 41056747 41056747 single base substitution G A 3_prime_UTR_variant LINC-JP X 41056747 41056747 single base substitution G A missense_variant G1455D 4364G>A LINC-JP X 41073231 41073231 single base substitution C A downstream_gene_variant LINC-JP X 41073231 41073231 single base substitution C A intron_variant LIRI-JP X 40940422 40940423 deletion of <=200bp AC - upstream_gene_variant LIRI-JP X 40942351 40942351 single base substitution G A upstream_gene_variant LIRI-JP X 40942526 40942526 single base substitution A G upstream_gene_variant LIRI-JP X 40943412 40943412 single base substitution C T upstream_gene_variant LIRI-JP X 40946693 40946693 single base substitution A G intron_variant LIRI-JP X 40947710 40947712 deletion of <=200bp ACA - intron_variant LIRI-JP X 40949094 40949094 single base substitution C T intron_variant LIRI-JP X 40950593 40950593 single base substitution A G intron_variant LIRI-JP X 40952030 40952030 single base substitution A T intron_variant LIRI-JP X 40952791 40952791 single base substitution T G intron_variant LIRI-JP X 40953716 40953716 single base substitution A G intron_variant LIRI-JP X 40953766 40953766 single base substitution G A intron_variant LIRI-JP X 40954153 40954153 single base substitution C T intron_variant LIRI-JP X 40954964 40954964 single base substitution A G intron_variant LIRI-JP X 40957692 40957692 single base substitution C A intron_variant LIRI-JP X 40958033 40958033 single base substitution T A intron_variant LIRI-JP X 40959757 40959757 single base substitution A G intron_variant LIRI-JP X 40961476 40961476 single base substitution G A intron_variant LIRI-JP X 40962347 40962347 single base substitution T A intron_variant LIRI-JP X 40963847 40963854 deletion of <=200bp TTATATTT - intron_variant LIRI-JP X 40967000 40967000 single base substitution C G intron_variant LIRI-JP X 40967745 40967745 single base substitution A T intron_variant LIRI-JP X 40967943 40967943 single base substitution G T intron_variant LIRI-JP X 40968770 40968770 single base substitution T C intron_variant LIRI-JP X 40970470 40970470 single base substitution A G intron_variant LIRI-JP X 40970717 40970717 single base substitution C T intron_variant LIRI-JP X 40971259 40971259 single base substitution C T intron_variant LIRI-JP X 40972063 40972063 single base substitution G T intron_variant LIRI-JP X 40978654 40978654 single base substitution A G intron_variant LIRI-JP X 40979274 40979274 single base substitution A G intron_variant LIRI-JP X 40984147 40984147 single base substitution A G intron_variant LIRI-JP X 40991774 40991774 single base substitution C G intron_variant LIRI-JP X 40993520 40993520 single base substitution T C intron_variant LIRI-JP X 40995600 40995600 single base substitution G A intron_variant LIRI-JP X 40999437 40999437 single base substitution T G intron_variant LIRI-JP X 41000313 41000313 single base substitution T C synonymous_variant L289L 865T>C LIRI-JP X 41000354 41000354 single base substitution C A synonymous_variant A302A 906C>A LIRI-JP X 41001500 41001500 single base substitution G C intron_variant LIRI-JP X 41001950 41001950 single base substitution A G intron_variant LIRI-JP X 41004300 41004300 single base substitution T A intron_variant LIRI-JP X 41005059 41005059 insertion of <=200bp - T intron_variant LIRI-JP X 41005434 41005435 deletion of <=200bp TC - intron_variant LIRI-JP X 41005898 41005898 single base substitution T G intron_variant LIRI-JP X 41007519 41007519 single base substitution A G intron_variant LIRI-JP X 41008636 41008636 single base substitution A G intron_variant LIRI-JP X 41008694 41008694 single base substitution T C intron_variant LIRI-JP X 41010159 41010159 single base substitution A G intron_variant LIRI-JP X 41012322 41012322 single base substitution C A missense_variant L629I 1885C>A LIRI-JP X 41013503 41013503 single base substitution A G intron_variant LIRI-JP X 41013564 41013564 single base substitution G A intron_variant LIRI-JP X 41014792 41014792 single base substitution T G intron_variant LIRI-JP X 41014986 41014987 deletion of <=200bp TG - intron_variant LIRI-JP X 41017119 41017119 single base substitution A G intron_variant LIRI-JP X 41019368 41019368 single base substitution A G intron_variant LIRI-JP X 41021444 41021444 single base substitution A G intron_variant LIRI-JP X 41021444 41021444 single base substitution A G upstream_gene_variant LIRI-JP X 41021557 41021557 single base substitution A G intron_variant LIRI-JP X 41021557 41021557 single base substitution A G upstream_gene_variant LIRI-JP X 41022140 41022140 single base substitution A G intron_variant LIRI-JP X 41022140 41022140 single base substitution A G upstream_gene_variant LIRI-JP X 41023376 41023376 single base substitution G A intron_variant LIRI-JP X 41023376 41023376 single base substitution G A upstream_gene_variant LIRI-JP X 41031885 41031885 single base substitution T C downstream_gene_variant LIRI-JP X 41031885 41031885 single base substitution T C intron_variant LIRI-JP X 41032413 41032413 single base substitution G A downstream_gene_variant LIRI-JP X 41032413 41032413 single base substitution G A intron_variant LIRI-JP X 41033486 41033486 single base substitution A G intron_variant LIRI-JP X 41034933 41034933 single base substitution T A intron_variant LIRI-JP X 41034994 41034994 single base substitution G A intron_variant LIRI-JP X 41037877 41037877 single base substitution G T intron_variant LIRI-JP X 41039154 41039154 single base substitution A G intron_variant LIRI-JP X 41039154 41039154 single base substitution A G upstream_gene_variant LIRI-JP X 41041441 41041441 single base substitution A G intron_variant LIRI-JP X 41041441 41041441 single base substitution A G upstream_gene_variant LIRI-JP X 41045537 41045537 single base substitution C A downstream_gene_variant LIRI-JP X 41045537 41045537 single base substitution C A intron_variant LIRI-JP X 41045537 41045537 single base substitution C A upstream_gene_variant LIRI-JP X 41046287 41046287 single base substitution T C downstream_gene_variant LIRI-JP X 41046287 41046287 single base substitution T C intron_variant LIRI-JP X 41046287 41046287 single base substitution T C upstream_gene_variant LIRI-JP X 41047536 41047536 single base substitution G A downstream_gene_variant LIRI-JP X 41047536 41047536 single base substitution G A intron_variant LIRI-JP X 41047650 41047650 single base substitution A G downstream_gene_variant LIRI-JP X 41047650 41047650 single base substitution A G intron_variant LIRI-JP X 41048275 41048275 single base substitution G C downstream_gene_variant LIRI-JP X 41048275 41048275 single base substitution G C intron_variant LIRI-JP X 41051314 41051314 single base substitution T A downstream_gene_variant LIRI-JP X 41051314 41051314 single base substitution T A intron_variant LIRI-JP X 41051314 41051314 single base substitution T A upstream_gene_variant LIRI-JP X 41052306 41052306 single base substitution A G downstream_gene_variant LIRI-JP X 41052306 41052306 single base substitution A G intron_variant LIRI-JP X 41052306 41052306 single base substitution A G upstream_gene_variant LIRI-JP X 41053118 41053118 single base substitution G T downstream_gene_variant LIRI-JP X 41053118 41053118 single base substitution G T intron_variant LIRI-JP X 41053118 41053118 single base substitution G T upstream_gene_variant LIRI-JP X 41053474 41053474 single base substitution A G downstream_gene_variant LIRI-JP X 41053474 41053474 single base substitution A G intron_variant LIRI-JP X 41053474 41053474 single base substitution A G upstream_gene_variant LIRI-JP X 41055251 41055251 single base substitution G C exon_variant LIRI-JP X 41055251 41055251 single base substitution G C intron_variant LIRI-JP X 41062094 41062094 single base substitution A G downstream_gene_variant LIRI-JP X 41062094 41062094 single base substitution A G intron_variant LIRI-JP X 41062094 41062094 single base substitution A G upstream_gene_variant LIRI-JP X 41062756 41062756 single base substitution A G downstream_gene_variant LIRI-JP X 41062756 41062756 single base substitution A G intron_variant LIRI-JP X 41062756 41062756 single base substitution A G upstream_gene_variant LIRI-JP X 41066200 41066200 single base substitution G A intron_variant LIRI-JP X 41066367 41066367 single base substitution A G intron_variant LIRI-JP X 41070019 41070020 deletion of <=200bp AA - downstream_gene_variant LIRI-JP X 41070019 41070020 deletion of <=200bp AA - intron_variant LIRI-JP X 41070108 41070108 single base substitution T C downstream_gene_variant LIRI-JP X 41070108 41070108 single base substitution T C intron_variant LIRI-JP X 41072900 41072900 single base substitution C G downstream_gene_variant LIRI-JP X 41072900 41072900 single base substitution C G intron_variant LIRI-JP X 41073093 41073093 single base substitution G A downstream_gene_variant LIRI-JP X 41073093 41073093 single base substitution G A intron_variant LIRI-JP X 41073705 41073705 single base substitution T A downstream_gene_variant LIRI-JP X 41073705 41073705 single base substitution T A intron_variant LIRI-JP X 41077636 41077636 single base substitution T A stop_gained L2074* 6221T>A LIRI-JP X 41077693 41077693 insertion of <=200bp - T frameshift_variant L2093L? LIRI-JP X 41077699 41077699 single base substitution A G missense_variant N2095S 6284A>G LIRI-JP X 41079138 41079138 single base substitution T G intron_variant LIRI-JP X 41081595 41081595 single base substitution G A intron_variant LIRI-JP X 41081998 41081998 single base substitution G A intron_variant LIRI-JP X 41082194 41082194 single base substitution G C intron_variant LIRI-JP X 41082489 41082489 single base substitution G A synonymous_variant Q2195Q 6585G>A LIRI-JP X 41082490 41082490 single base substitution C T missense_variant L2196F 6586C>T LIRI-JP X 41082795 41082795 single base substitution A G intron_variant LIRI-JP X 41083335 41083335 single base substitution C T intron_variant LIRI-JP X 41083335 41083335 single base substitution C T upstream_gene_variant LIRI-JP X 41084348 41084348 single base substitution T G missense_variant L2340R 7019T>G LIRI-JP X 41084348 41084348 single base substitution T G upstream_gene_variant LIRI-JP X 41085103 41085103 single base substitution G A intron_variant LIRI-JP X 41085103 41085103 single base substitution G A upstream_gene_variant LIRI-JP X 41085568 41085568 single base substitution A G intron_variant LIRI-JP X 41085568 41085568 single base substitution A G upstream_gene_variant LIRI-JP X 41087933 41087934 deletion of <=200bp TG - intron_variant LIRI-JP X 41087933 41087934 deletion of <=200bp TG - upstream_gene_variant LIRI-JP X 41087947 41087948 deletion of <=200bp AT - intron_variant LIRI-JP X 41087947 41087948 deletion of <=200bp AT - upstream_gene_variant LIRI-JP X 41088973 41088973 single base substitution G T exon_variant LIRI-JP X 41088973 41088973 single base substitution G T stop_gained E2458* 7372G>T LIRI-JP X 41090248 41090248 single base substitution T C downstream_gene_variant LIRI-JP X 41090248 41090248 single base substitution T C intron_variant LIRI-JP X 41091553 41091553 single base substitution T A downstream_gene_variant LIRI-JP X 41091553 41091553 single base substitution T A intron_variant LIRI-JP X 41091555 41091555 single base substitution C A downstream_gene_variant LIRI-JP X 41091555 41091555 single base substitution C A intron_variant LIRI-JP X 41093075 41093075 single base substitution A G 3_prime_UTR_variant LIRI-JP X 41093075 41093075 single base substitution A G downstream_gene_variant LIRI-JP X 41094633 41094633 single base substitution G A 3_prime_UTR_variant LIRI-JP X 41094633 41094633 single base substitution G A downstream_gene_variant LIRI-JP X 41095087 41095087 single base substitution A G 3_prime_UTR_variant LIRI-JP X 41095087 41095087 single base substitution A G downstream_gene_variant LIRI-JP X 41097388 41097388 single base substitution G A downstream_gene_variant LUSC-KR X 40940745 40940745 single base substitution A T upstream_gene_variant LUSC-KR X 40956451 40956451 single base substitution T C intron_variant LUSC-KR X 40957975 40957975 single base substitution A T intron_variant LUSC-KR X 40972813 40972813 single base substitution G A intron_variant LUSC-KR X 40982326 40982326 single base substitution G A intron_variant LUSC-KR X 40984056 40984056 single base substitution A G intron_variant LUSC-KR X 40987529 40987529 single base substitution G T intron_variant LUSC-KR X 40991141 40991141 single base substitution A G intron_variant LUSC-KR X 40996363 40996363 single base substitution C A intron_variant LUSC-KR X 40996919 40996919 single base substitution A T intron_variant LUSC-KR X 40998336 40998336 single base substitution G T intron_variant LUSC-KR X 41003868 41003868 single base substitution G T missense_variant D470Y 1408G>T LUSC-KR X 41023004 41023004 single base substitution T A intron_variant LUSC-KR X 41023004 41023004 single base substitution T A upstream_gene_variant LUSC-KR X 41029880 41029880 single base substitution G C downstream_gene_variant LUSC-KR X 41029880 41029880 single base substitution G C splice_region_variant LUSC-KR X 41036702 41036702 single base substitution A T intron_variant LUSC-KR X 41043214 41043214 single base substitution G A intron_variant LUSC-KR X 41043214 41043214 single base substitution G A upstream_gene_variant LUSC-KR X 41046489 41046489 single base substitution G A downstream_gene_variant LUSC-KR X 41046489 41046489 single base substitution G A intron_variant LUSC-KR X 41046489 41046489 single base substitution G A upstream_gene_variant LUSC-KR X 41057160 41057160 single base substitution G C intron_variant LUSC-KR X 41065666 41065666 single base substitution A T intron_variant LUSC-KR X 41070746 41070746 single base substitution G A downstream_gene_variant LUSC-KR X 41070746 41070746 single base substitution G A intron_variant LUSC-KR X 41071157 41071157 single base substitution G A downstream_gene_variant LUSC-KR X 41071157 41071157 single base substitution G A intron_variant LUSC-KR X 41071181 41071181 single base substitution C T downstream_gene_variant LUSC-KR X 41071181 41071181 single base substitution C T intron_variant LUSC-KR X 41071202 41071202 single base substitution G A downstream_gene_variant LUSC-KR X 41071202 41071202 single base substitution G A intron_variant LUSC-KR X 41071278 41071278 single base substitution G A downstream_gene_variant LUSC-KR X 41071278 41071278 single base substitution G A intron_variant LUSC-KR X 41071282 41071282 single base substitution G A downstream_gene_variant LUSC-KR X 41071282 41071282 single base substitution G A intron_variant LUSC-KR X 41071333 41071333 single base substitution G A downstream_gene_variant LUSC-KR X 41071333 41071333 single base substitution G A intron_variant LUSC-KR X 41071440 41071440 single base substitution T A downstream_gene_variant LUSC-KR X 41071440 41071440 single base substitution T A intron_variant LUSC-KR X 41071462 41071462 single base substitution G A downstream_gene_variant LUSC-KR X 41071462 41071462 single base substitution G A intron_variant LUSC-KR X 41071513 41071513 single base substitution G C downstream_gene_variant LUSC-KR X 41071513 41071513 single base substitution G C intron_variant LUSC-KR X 41072843 41072843 single base substitution G T downstream_gene_variant LUSC-KR X 41072843 41072843 single base substitution G T intron_variant LUSC-KR X 41082361 41082361 single base substitution G A intron_variant LUSC-KR X 41089611 41089611 single base substitution C T downstream_gene_variant LUSC-KR X 41089611 41089611 single base substitution C T intron_variant LUSC-KR X 41089640 41089640 single base substitution A G downstream_gene_variant LUSC-KR X 41089640 41089640 single base substitution A G intron_variant LUSC-KR X 41092297 41092297 single base substitution G T 3_prime_UTR_variant LUSC-KR X 41092297 41092297 single base substitution G T downstream_gene_variant LUSC-US X 40994071 40994071 single base substitution G T missense_variant G139V 416G>T LUSC-US X 41000371 41000371 single base substitution C A stop_gained S308* 923C>A LUSC-US X 41010252 41010252 single base substitution G C missense_variant A569P 1705G>C LUSC-US X 41026799 41026799 single base substitution C T exon_variant LUSC-US X 41026799 41026799 single base substitution C T missense_variant T798M 2393C>T LUSC-US X 41056655 41056655 single base substitution G C 3_prime_UTR_variant LUSC-US X 41056655 41056655 single base substitution G C missense_variant E1424D 4272G>C LUSC-US X 41064718 41064718 single base substitution G C exon_variant LUSC-US X 41064718 41064718 single base substitution G C missense_variant V1663L 4987G>C LUSC-US X 41075504 41075504 insertion of <=200bp - T frameshift_variant N1895I? LUSC-US X 41075634 41075634 insertion of <=200bp - T frameshift_variant S1938S? LUSC-US X 41075775 41075775 single base substitution A T synonymous_variant S1985S 5955A>T LUSC-US X 41078486 41078486 single base substitution T A splice_donor_variant MALY-DE X 40941994 40941995 deletion of <=200bp AT - upstream_gene_variant MALY-DE X 40943683 40943683 single base substitution G A upstream_gene_variant MALY-DE X 40945123 40945125 deletion of <=200bp AGG - 5_prime_UTR_variant MALY-DE X 40946857 40946857 single base substitution T G intron_variant MALY-DE X 40950738 40950738 single base substitution A G intron_variant MALY-DE X 40956658 40956658 single base substitution G T intron_variant MALY-DE X 40963087 40963087 single base substitution T G intron_variant MALY-DE X 40965773 40965773 single base substitution T A intron_variant MALY-DE X 40971573 40971573 single base substitution G A intron_variant MALY-DE X 40976271 40976271 single base substitution C T intron_variant MALY-DE X 40976791 40976791 single base substitution A T intron_variant MALY-DE X 40990778 40990778 single base substitution T C missense_variant L104P 311T>C MALY-DE X 40990840 40990840 single base substitution T C intron_variant MALY-DE X 40990842 40990842 single base substitution T A intron_variant MALY-DE X 40990897 40990897 single base substitution A G intron_variant MALY-DE X 41000039 41000039 single base substitution A G intron_variant MALY-DE X 41005906 41005906 single base substitution G A intron_variant MALY-DE X 41009712 41009712 single base substitution T A intron_variant MALY-DE X 41009731 41009731 single base substitution T G intron_variant MALY-DE X 41009776 41009776 single base substitution T A intron_variant MALY-DE X 41045585 41045585 single base substitution A G downstream_gene_variant MALY-DE X 41045585 41045585 single base substitution A G intron_variant MALY-DE X 41045585 41045585 single base substitution A G upstream_gene_variant MALY-DE X 41055103 41055103 single base substitution C A intron_variant MALY-DE X 41055103 41055103 single base substitution C A upstream_gene_variant MALY-DE X 41077766 41077766 single base substitution A G synonymous_variant A2117A 6351A>G MALY-DE X 41087768 41087768 single base substitution T G intron_variant MALY-DE X 41087768 41087768 single base substitution T G upstream_gene_variant MELA-AU X 40940239 40940239 single base substitution C T upstream_gene_variant MELA-AU X 40941214 40941214 single base substitution C T upstream_gene_variant MELA-AU X 40941412 40941412 single base substitution G A upstream_gene_variant MELA-AU X 40941443 40941443 single base substitution G A upstream_gene_variant MELA-AU X 40942020 40942020 single base substitution T G upstream_gene_variant MELA-AU X 40942475 40942475 single base substitution C T upstream_gene_variant MELA-AU X 40942823 40942823 single base substitution C G upstream_gene_variant MELA-AU X 40943798 40943799 multiple base substitution (>=2bp and <=200bp) CC TG upstream_gene_variant MELA-AU X 40943994 40943994 single base substitution C T upstream_gene_variant MELA-AU X 40945808 40945808 single base substitution G A intron_variant MELA-AU X 40949808 40949808 single base substitution C T intron_variant MELA-AU X 40949963 40949963 single base substitution C T intron_variant MELA-AU X 40950666 40950666 single base substitution A G intron_variant MELA-AU X 40951138 40951138 single base substitution C T intron_variant MELA-AU X 40951990 40951990 single base substitution G A intron_variant MELA-AU X 40952720 40952720 single base substitution C G intron_variant MELA-AU X 40954209 40954209 single base substitution C T intron_variant MELA-AU X 40956295 40956295 insertion of <=200bp - TG intron_variant MELA-AU X 40958153 40958153 single base substitution C T intron_variant MELA-AU X 40958393 40958393 single base substitution C T intron_variant MELA-AU X 40959373 40959373 single base substitution T C intron_variant MELA-AU X 40959404 40959404 single base substitution T G intron_variant MELA-AU X 40960592 40960592 single base substitution G A intron_variant MELA-AU X 40961314 40961314 single base substitution C T intron_variant MELA-AU X 40961619 40961619 single base substitution C T intron_variant MELA-AU X 40961723 40961723 deletion of <=200bp T - intron_variant MELA-AU X 40963234 40963234 single base substitution C T intron_variant MELA-AU X 40963579 40963579 single base substitution C T intron_variant MELA-AU X 40963644 40963644 single base substitution T C intron_variant MELA-AU X 40963921 40963921 single base substitution G A intron_variant MELA-AU X 40964968 40964968 single base substitution A C intron_variant MELA-AU X 40965437 40965437 single base substitution T C intron_variant MELA-AU X 40966391 40966391 single base substitution C T intron_variant MELA-AU X 40966735 40966736 multiple base substitution (>=2bp and <=200bp) TG AT intron_variant MELA-AU X 40966777 40966777 single base substitution C T intron_variant MELA-AU X 40966971 40966971 single base substitution C T intron_variant MELA-AU X 40967958 40967959 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU X 40970682 40970682 insertion of <=200bp - AA intron_variant MELA-AU X 40970708 40970708 single base substitution C T intron_variant MELA-AU X 40971546 40971546 single base substitution T C intron_variant MELA-AU X 40972419 40972419 single base substitution C T intron_variant MELA-AU X 40973505 40973505 single base substitution C T intron_variant MELA-AU X 40973760 40973760 single base substitution A C intron_variant MELA-AU X 40973994 40973994 single base substitution C T intron_variant MELA-AU X 40974032 40974032 single base substitution C T intron_variant MELA-AU X 40976749 40976749 single base substitution A G intron_variant MELA-AU X 40976804 40976804 single base substitution A G intron_variant MELA-AU X 40977179 40977179 single base substitution C T intron_variant MELA-AU X 40978790 40978790 single base substitution C T intron_variant MELA-AU X 40980788 40980788 single base substitution T G intron_variant MELA-AU X 40982108 40982108 single base substitution C T intron_variant MELA-AU X 40982708 40982708 single base substitution C T intron_variant MELA-AU X 40983842 40983842 single base substitution C T intron_variant MELA-AU X 40984622 40984622 single base substitution C T intron_variant MELA-AU X 40984661 40984661 single base substitution T C intron_variant MELA-AU X 40985261 40985261 single base substitution G T intron_variant MELA-AU X 40986886 40986886 single base substitution G A intron_variant MELA-AU X 40987128 40987128 single base substitution T G intron_variant MELA-AU X 40988090 40988090 single base substitution C T intron_variant MELA-AU X 40988418 40988418 single base substitution C T intron_variant MELA-AU X 40988447 40988447 single base substitution C T intron_variant MELA-AU X 40990236 40990236 single base substitution C T intron_variant MELA-AU X 40990661 40990661 single base substitution C T intron_variant MELA-AU X 40992483 40992483 single base substitution C T intron_variant MELA-AU X 40993794 40993794 single base substitution C T intron_variant MELA-AU X 40994832 40994832 single base substitution G A intron_variant MELA-AU X 40995324 40995324 single base substitution G A intron_variant MELA-AU X 40996412 40996412 single base substitution C T intron_variant MELA-AU X 40996530 40996530 single base substitution T A intron_variant MELA-AU X 40998504 40998504 single base substitution T A intron_variant MELA-AU X 40999084 40999084 single base substitution C A intron_variant MELA-AU X 41000563 41000563 single base substitution C T missense_variant S347F 1040C>T MELA-AU X 41000832 41000832 single base substitution C T intron_variant MELA-AU X 41005816 41005816 single base substitution T G intron_variant MELA-AU X 41007227 41007227 single base substitution C T intron_variant MELA-AU X 41007829 41007829 single base substitution G A splice_donor_variant MELA-AU X 41008103 41008103 single base substitution C T intron_variant MELA-AU X 41008202 41008202 single base substitution C T intron_variant MELA-AU X 41009290 41009290 single base substitution C T intron_variant MELA-AU X 41009441 41009441 single base substitution C T intron_variant MELA-AU X 41009880 41009880 single base substitution C T intron_variant MELA-AU X 41009929 41009929 single base substitution C G intron_variant MELA-AU X 41010547 41010547 single base substitution T C intron_variant MELA-AU X 41011015 41011015 single base substitution C T intron_variant MELA-AU X 41012127 41012127 single base substitution T C intron_variant MELA-AU X 41014071 41014071 single base substitution C T intron_variant MELA-AU X 41014231 41014231 single base substitution C T intron_variant MELA-AU X 41014859 41014859 single base substitution A G intron_variant MELA-AU X 41015366 41015366 single base substitution G A intron_variant MELA-AU X 41016690 41016690 single base substitution A G intron_variant MELA-AU X 41017504 41017504 single base substitution A C intron_variant MELA-AU X 41018040 41018040 single base substitution C T intron_variant MELA-AU X 41018636 41018636 single base substitution C T intron_variant MELA-AU X 41019002 41019002 single base substitution C T intron_variant MELA-AU X 41019258 41019258 single base substitution T G intron_variant MELA-AU X 41019738 41019738 single base substitution C T intron_variant MELA-AU X 41019990 41019990 single base substitution C T intron_variant MELA-AU X 41020078 41020078 single base substitution C T intron_variant MELA-AU X 41020378 41020378 single base substitution C T intron_variant MELA-AU X 41020623 41020623 single base substitution C T intron_variant MELA-AU X 41020951 41020951 single base substitution G A intron_variant MELA-AU X 41021158 41021158 single base substitution G A intron_variant MELA-AU X 41021194 41021194 single base substitution C T intron_variant MELA-AU X 41021818 41021818 single base substitution T G intron_variant MELA-AU X 41021818 41021818 single base substitution T G upstream_gene_variant MELA-AU X 41023027 41023027 single base substitution C T intron_variant MELA-AU X 41023027 41023027 single base substitution C T upstream_gene_variant MELA-AU X 41023095 41023095 single base substitution C T intron_variant MELA-AU X 41023095 41023095 single base substitution C T upstream_gene_variant MELA-AU X 41023539 41023539 single base substitution G A intron_variant MELA-AU X 41023539 41023539 single base substitution G A upstream_gene_variant MELA-AU X 41024173 41024173 single base substitution C T intron_variant MELA-AU X 41024173 41024173 single base substitution C T upstream_gene_variant MELA-AU X 41024437 41024438 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU X 41024437 41024438 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU X 41024504 41024504 single base substitution A G intron_variant MELA-AU X 41024504 41024504 single base substitution A G upstream_gene_variant MELA-AU X 41024864 41024864 single base substitution C T intron_variant MELA-AU X 41024864 41024864 single base substitution C T upstream_gene_variant MELA-AU X 41025219 41025219 single base substitution C T missense_variant R694C 2080C>T MELA-AU X 41025219 41025219 single base substitution C T upstream_gene_variant MELA-AU X 41025346 41025346 single base substitution G A missense_variant G736E 2207G>A MELA-AU X 41025346 41025346 single base substitution G A upstream_gene_variant MELA-AU X 41025515 41025515 single base substitution C T intron_variant MELA-AU X 41025515 41025515 single base substitution C T upstream_gene_variant MELA-AU X 41026287 41026287 single base substitution C T intron_variant MELA-AU X 41026287 41026287 single base substitution C T upstream_gene_variant MELA-AU X 41026505 41026505 single base substitution T A exon_variant MELA-AU X 41026505 41026505 single base substitution T A intron_variant MELA-AU X 41027340 41027340 single base substitution T G exon_variant MELA-AU X 41027340 41027340 single base substitution T G synonymous_variant G835G 2505T>G MELA-AU X 41027823 41027823 single base substitution A T downstream_gene_variant MELA-AU X 41027823 41027823 single base substitution A T intron_variant MELA-AU X 41029375 41029375 single base substitution C T downstream_gene_variant MELA-AU X 41029375 41029375 single base substitution C T missense_variant R922C 2764C>T MELA-AU X 41029487 41029487 single base substitution C T downstream_gene_variant MELA-AU X 41029487 41029487 single base substitution C T missense_variant S959L 2876C>T MELA-AU X 41029645 41029645 single base substitution T C downstream_gene_variant MELA-AU X 41029645 41029645 single base substitution T C intron_variant MELA-AU X 41030287 41030287 single base substitution G A downstream_gene_variant MELA-AU X 41030287 41030287 single base substitution G A intron_variant MELA-AU X 41031320 41031320 single base substitution T C downstream_gene_variant MELA-AU X 41031320 41031320 single base substitution T C intron_variant MELA-AU X 41031954 41031954 single base substitution C T downstream_gene_variant MELA-AU X 41031954 41031954 single base substitution C T intron_variant MELA-AU X 41032018 41032019 multiple base substitution (>=2bp and <=200bp) TG AC downstream_gene_variant MELA-AU X 41032018 41032019 multiple base substitution (>=2bp and <=200bp) TG AC intron_variant MELA-AU X 41035027 41035027 single base substitution C T intron_variant MELA-AU X 41035972 41035972 single base substitution A T intron_variant MELA-AU X 41037445 41037445 single base substitution C T intron_variant MELA-AU X 41037674 41037674 single base substitution C T intron_variant MELA-AU X 41038389 41038389 single base substitution C G intron_variant MELA-AU X 41038389 41038389 single base substitution C G upstream_gene_variant MELA-AU X 41038416 41038416 single base substitution C A intron_variant MELA-AU X 41038416 41038416 single base substitution C A upstream_gene_variant MELA-AU X 41038450 41038450 single base substitution C G intron_variant MELA-AU X 41038450 41038450 single base substitution C G upstream_gene_variant MELA-AU X 41038534 41038534 single base substitution C T intron_variant MELA-AU X 41038534 41038534 single base substitution C T upstream_gene_variant MELA-AU X 41038718 41038718 single base substitution C T intron_variant MELA-AU X 41038718 41038718 single base substitution C T upstream_gene_variant MELA-AU X 41039348 41039348 single base substitution C T intron_variant MELA-AU X 41039348 41039348 single base substitution C T upstream_gene_variant MELA-AU X 41039351 41039351 single base substitution C A intron_variant MELA-AU X 41039351 41039351 single base substitution C A upstream_gene_variant MELA-AU X 41039448 41039448 single base substitution C T intron_variant MELA-AU X 41039448 41039448 single base substitution C T upstream_gene_variant MELA-AU X 41039498 41039498 single base substitution C T intron_variant MELA-AU X 41039498 41039498 single base substitution C T upstream_gene_variant MELA-AU X 41040016 41040016 single base substitution C T intron_variant MELA-AU X 41040016 41040016 single base substitution C T upstream_gene_variant MELA-AU X 41040447 41040447 single base substitution T C intron_variant MELA-AU X 41040447 41040447 single base substitution T C upstream_gene_variant MELA-AU X 41041359 41041359 single base substitution C T intron_variant MELA-AU X 41041359 41041359 single base substitution C T upstream_gene_variant MELA-AU X 41041652 41041652 single base substitution C T intron_variant MELA-AU X 41041652 41041652 single base substitution C T upstream_gene_variant MELA-AU X 41042114 41042114 single base substitution A T intron_variant MELA-AU X 41042114 41042114 single base substitution A T upstream_gene_variant MELA-AU X 41042175 41042175 single base substitution C T intron_variant MELA-AU X 41042175 41042175 single base substitution C T upstream_gene_variant MELA-AU X 41043646 41043646 single base substitution C T intron_variant MELA-AU X 41043646 41043646 single base substitution C T splice_region_variant MELA-AU X 41043646 41043646 single base substitution C T upstream_gene_variant MELA-AU X 41043727 41043727 single base substitution A T exon_variant MELA-AU X 41043727 41043727 single base substitution A T missense_variant K1119N 3357A>T MELA-AU X 41043727 41043727 single base substitution A T upstream_gene_variant MELA-AU X 41043952 41043952 single base substitution C T exon_variant MELA-AU X 41043952 41043952 single base substitution C T intron_variant MELA-AU X 41043952 41043952 single base substitution C T upstream_gene_variant MELA-AU X 41044258 41044258 single base substitution C T downstream_gene_variant MELA-AU X 41044258 41044258 single base substitution C T intron_variant MELA-AU X 41044258 41044258 single base substitution C T upstream_gene_variant MELA-AU X 41044422 41044422 single base substitution C T downstream_gene_variant MELA-AU X 41044422 41044422 single base substitution C T intron_variant MELA-AU X 41044422 41044422 single base substitution C T upstream_gene_variant MELA-AU X 41045336 41045336 single base substitution C T downstream_gene_variant MELA-AU X 41045336 41045336 single base substitution C T intron_variant MELA-AU X 41045336 41045336 single base substitution C T upstream_gene_variant MELA-AU X 41045833 41045833 single base substitution C T downstream_gene_variant MELA-AU X 41045833 41045833 single base substitution C T missense_variant P1208S 3622C>T MELA-AU X 41045833 41045833 single base substitution C T upstream_gene_variant MELA-AU X 41047542 41047542 single base substitution G A downstream_gene_variant MELA-AU X 41047542 41047542 single base substitution G A intron_variant MELA-AU X 41050609 41050609 single base substitution C T downstream_gene_variant MELA-AU X 41050609 41050609 single base substitution C T intron_variant MELA-AU X 41050609 41050609 single base substitution C T upstream_gene_variant MELA-AU X 41050743 41050743 single base substitution C T downstream_gene_variant MELA-AU X 41050743 41050743 single base substitution C T intron_variant MELA-AU X 41050743 41050743 single base substitution C T upstream_gene_variant MELA-AU X 41050918 41050918 single base substitution C T downstream_gene_variant MELA-AU X 41050918 41050918 single base substitution C T intron_variant MELA-AU X 41050918 41050918 single base substitution C T upstream_gene_variant MELA-AU X 41051237 41051237 single base substitution A G downstream_gene_variant MELA-AU X 41051237 41051237 single base substitution A G intron_variant MELA-AU X 41051237 41051237 single base substitution A G upstream_gene_variant MELA-AU X 41051266 41051266 single base substitution C T downstream_gene_variant MELA-AU X 41051266 41051266 single base substitution C T intron_variant MELA-AU X 41051266 41051266 single base substitution C T upstream_gene_variant MELA-AU X 41052167 41052167 single base substitution C T downstream_gene_variant MELA-AU X 41052167 41052167 single base substitution C T intron_variant MELA-AU X 41052167 41052167 single base substitution C T upstream_gene_variant MELA-AU X 41052555 41052555 single base substitution T A downstream_gene_variant MELA-AU X 41052555 41052555 single base substitution T A intron_variant MELA-AU X 41052555 41052555 single base substitution T A upstream_gene_variant MELA-AU X 41053378 41053378 single base substitution C T downstream_gene_variant MELA-AU X 41053378 41053378 single base substitution C T intron_variant MELA-AU X 41053378 41053378 single base substitution C T upstream_gene_variant MELA-AU X 41053932 41053932 single base substitution C T downstream_gene_variant MELA-AU X 41053932 41053932 single base substitution C T intron_variant MELA-AU X 41053932 41053932 single base substitution C T upstream_gene_variant MELA-AU X 41053999 41053999 single base substitution C T downstream_gene_variant MELA-AU X 41053999 41053999 single base substitution C T intron_variant MELA-AU X 41053999 41053999 single base substitution C T upstream_gene_variant MELA-AU X 41054814 41054814 single base substitution G A intron_variant MELA-AU X 41054814 41054814 single base substitution G A upstream_gene_variant MELA-AU X 41054862 41054862 single base substitution G A intron_variant MELA-AU X 41054862 41054862 single base substitution G A upstream_gene_variant MELA-AU X 41054876 41054876 single base substitution A C intron_variant MELA-AU X 41054876 41054876 single base substitution A C upstream_gene_variant MELA-AU X 41057683 41057683 single base substitution C T intron_variant MELA-AU X 41058569 41058569 single base substitution A T downstream_gene_variant MELA-AU X 41058569 41058569 single base substitution A T intron_variant MELA-AU X 41058723 41058723 single base substitution G C downstream_gene_variant MELA-AU X 41058723 41058723 single base substitution G C intron_variant MELA-AU X 41058750 41058751 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU X 41058750 41058751 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU X 41061252 41061252 single base substitution C T downstream_gene_variant MELA-AU X 41061252 41061252 single base substitution C T intron_variant MELA-AU X 41061252 41061252 single base substitution C T upstream_gene_variant MELA-AU X 41061948 41061948 single base substitution C T downstream_gene_variant MELA-AU X 41061948 41061948 single base substitution C T intron_variant MELA-AU X 41061948 41061948 single base substitution C T upstream_gene_variant MELA-AU X 41061998 41061998 single base substitution C T downstream_gene_variant MELA-AU X 41061998 41061998 single base substitution C T intron_variant MELA-AU X 41061998 41061998 single base substitution C T upstream_gene_variant MELA-AU X 41063804 41063804 single base substitution C T intron_variant MELA-AU X 41063804 41063804 single base substitution C T upstream_gene_variant MELA-AU X 41064916 41064916 single base substitution G A intron_variant MELA-AU X 41065365 41065365 single base substitution C T intron_variant MELA-AU X 41066563 41066563 single base substitution C T intron_variant MELA-AU X 41067009 41067009 single base substitution C G intron_variant MELA-AU X 41068100 41068100 single base substitution A G intron_variant MELA-AU X 41068831 41068831 single base substitution C T intron_variant MELA-AU X 41069529 41069529 single base substitution T C intron_variant MELA-AU X 41070098 41070098 single base substitution C T downstream_gene_variant MELA-AU X 41070098 41070098 single base substitution C T intron_variant MELA-AU X 41070761 41070761 single base substitution C T downstream_gene_variant MELA-AU X 41070761 41070761 single base substitution C T intron_variant MELA-AU X 41070934 41070934 single base substitution C T downstream_gene_variant MELA-AU X 41070934 41070934 single base substitution C T intron_variant MELA-AU X 41070966 41070966 single base substitution G A downstream_gene_variant MELA-AU X 41070966 41070966 single base substitution G A intron_variant MELA-AU X 41072776 41072776 single base substitution C T downstream_gene_variant MELA-AU X 41072776 41072776 single base substitution C T intron_variant MELA-AU X 41073221 41073221 single base substitution C T downstream_gene_variant MELA-AU X 41073221 41073221 single base substitution C T intron_variant MELA-AU X 41073305 41073305 single base substitution C T downstream_gene_variant MELA-AU X 41073305 41073305 single base substitution C T intron_variant MELA-AU X 41073813 41073813 single base substitution G A downstream_gene_variant MELA-AU X 41073813 41073813 single base substitution G A splice_region_variant MELA-AU X 41074472 41074472 single base substitution G T downstream_gene_variant MELA-AU X 41074472 41074472 single base substitution G T intron_variant MELA-AU X 41074506 41074506 single base substitution C T downstream_gene_variant MELA-AU X 41074506 41074506 single base substitution C T intron_variant MELA-AU X 41077249 41077249 single base substitution A G intron_variant MELA-AU X 41077600 41077600 single base substitution C G intron_variant MELA-AU X 41077726 41077726 single base substitution T C missense_variant L2104P 6311T>C MELA-AU X 41078204 41078204 single base substitution C T intron_variant MELA-AU X 41079237 41079237 single base substitution C T intron_variant MELA-AU X 41079882 41079882 single base substitution C T intron_variant MELA-AU X 41079958 41079958 single base substitution G A intron_variant MELA-AU X 41080437 41080437 single base substitution C T intron_variant MELA-AU X 41080959 41080959 single base substitution C T intron_variant MELA-AU X 41080982 41080982 single base substitution A G intron_variant MELA-AU X 41081180 41081180 single base substitution G C intron_variant MELA-AU X 41081484 41081484 single base substitution C T intron_variant MELA-AU X 41082225 41082225 single base substitution T A intron_variant MELA-AU X 41082439 41082441 deletion of <=200bp TTC - intron_variant MELA-AU X 41082886 41082886 single base substitution C T intron_variant MELA-AU X 41083250 41083250 single base substitution G A intron_variant MELA-AU X 41083250 41083250 single base substitution G A upstream_gene_variant MELA-AU X 41083718 41083718 single base substitution T G intron_variant MELA-AU X 41083718 41083718 single base substitution T G upstream_gene_variant MELA-AU X 41084009 41084009 deletion of <=200bp C - frameshift_variant P2256 MELA-AU X 41084009 41084009 deletion of <=200bp C - upstream_gene_variant MELA-AU X 41084140 41084140 single base substitution C G synonymous_variant T2299T 6897C>G MELA-AU X 41084140 41084140 single base substitution C G upstream_gene_variant MELA-AU X 41084548 41084548 single base substitution C T intron_variant MELA-AU X 41084548 41084548 single base substitution C T upstream_gene_variant MELA-AU X 41085255 41085255 single base substitution A G intron_variant MELA-AU X 41085255 41085255 single base substitution A G upstream_gene_variant MELA-AU X 41085476 41085476 single base substitution C T intron_variant MELA-AU X 41085476 41085476 single base substitution C T upstream_gene_variant MELA-AU X 41085962 41085962 single base substitution A T intron_variant MELA-AU X 41085962 41085962 single base substitution A T upstream_gene_variant MELA-AU X 41086491 41086491 single base substitution A G intron_variant MELA-AU X 41086491 41086491 single base substitution A G upstream_gene_variant MELA-AU X 41086972 41086974 multiple base substitution (>=2bp and <=200bp) GAG TTA intron_variant MELA-AU X 41086972 41086974 multiple base substitution (>=2bp and <=200bp) GAG TTA upstream_gene_variant MELA-AU X 41087190 41087190 single base substitution T G intron_variant MELA-AU X 41087190 41087190 single base substitution T G upstream_gene_variant MELA-AU X 41087246 41087246 single base substitution C T intron_variant MELA-AU X 41087246 41087246 single base substitution C T upstream_gene_variant MELA-AU X 41087960 41087960 single base substitution T A intron_variant MELA-AU X 41087960 41087960 single base substitution T A upstream_gene_variant MELA-AU X 41088889 41088889 single base substitution C T exon_variant MELA-AU X 41088889 41088889 single base substitution C T missense_variant P2430S 7288C>T MELA-AU X 41090267 41090267 single base substitution C T downstream_gene_variant MELA-AU X 41090267 41090267 single base substitution C T intron_variant MELA-AU X 41091752 41091752 single base substitution C T downstream_gene_variant MELA-AU X 41091752 41091752 single base substitution C T missense_variant S2547F 7640C>T MELA-AU X 41091752 41091752 single base substitution C T missense_variant S2563F 7688C>T MELA-AU X 41093413 41093413 single base substitution A T 3_prime_UTR_variant MELA-AU X 41093413 41093413 single base substitution A T downstream_gene_variant MELA-AU X 41093833 41093833 single base substitution G A 3_prime_UTR_variant MELA-AU X 41093833 41093833 single base substitution G A downstream_gene_variant MELA-AU X 41094530 41094530 single base substitution C A 3_prime_UTR_variant MELA-AU X 41094530 41094530 single base substitution C A downstream_gene_variant MELA-AU X 41095443 41095443 single base substitution C T 3_prime_UTR_variant MELA-AU X 41095443 41095443 single base substitution C T downstream_gene_variant MELA-AU X 41095843 41095843 single base substitution C T downstream_gene_variant MELA-AU X 41096580 41096580 single base substitution C T downstream_gene_variant MELA-AU X 41096782 41096782 single base substitution C T downstream_gene_variant MELA-AU X 41097034 41097034 single base substitution A G downstream_gene_variant MELA-AU X 41097298 41097298 single base substitution C T downstream_gene_variant MELA-AU X 41098332 41098332 single base substitution C T downstream_gene_variant MELA-AU X 41098473 41098473 single base substitution G A downstream_gene_variant MELA-AU X 41099190 41099190 single base substitution G A downstream_gene_variant MELA-AU X 41099226 41099226 single base substitution G T downstream_gene_variant MELA-AU X 41099669 41099669 single base substitution C T downstream_gene_variant MELA-AU X 41099711 41099711 single base substitution T C downstream_gene_variant MELA-AU X 41100205 41100205 single base substitution G A downstream_gene_variant ORCA-IN X 40939924 40939924 single base substitution C T upstream_gene_variant ORCA-IN X 40948019 40948019 deletion of <=200bp T - intron_variant ORCA-IN X 40952133 40952133 deletion of <=200bp T - intron_variant ORCA-IN X 40957864 40957864 single base substitution G T intron_variant ORCA-IN X 40960016 40960016 single base substitution C T intron_variant ORCA-IN X 40960677 40960677 deletion of <=200bp A - intron_variant ORCA-IN X 40971098 40971098 deletion of <=200bp T - intron_variant ORCA-IN X 40973739 40973739 insertion of <=200bp - T intron_variant ORCA-IN X 40974495 40974495 single base substitution G A intron_variant ORCA-IN X 40980094 40980094 deletion of <=200bp T - intron_variant ORCA-IN X 40983027 40983027 single base substitution G T intron_variant ORCA-IN X 40989727 40989727 deletion of <=200bp T - intron_variant ORCA-IN X 40994078 40994078 single base substitution G T missense_variant K141N 423G>T ORCA-IN X 40996157 40996157 single base substitution A G missense_variant N179S 536A>G ORCA-IN X 40997135 40997135 deletion of <=200bp T - intron_variant ORCA-IN X 41000444 41000444 insertion of <=200bp - AT frameshift_variant E332E? ORCA-IN X 41002622 41002622 single base substitution G T stop_gained E414* 1240G>T ORCA-IN X 41006428 41006428 insertion of <=200bp - T intron_variant ORCA-IN X 41006429 41006429 deletion of <=200bp T - intron_variant ORCA-IN X 41008964 41008964 deletion of <=200bp T - intron_variant ORCA-IN X 41009404 41009404 insertion of <=200bp - A intron_variant ORCA-IN X 41009405 41009405 deletion of <=200bp A - intron_variant ORCA-IN X 41010311 41010311 single base substitution G T splice_donor_variant ORCA-IN X 41018778 41018778 insertion of <=200bp - T intron_variant ORCA-IN X 41018950 41018950 deletion of <=200bp T - intron_variant ORCA-IN X 41021009 41021009 deletion of <=200bp T - intron_variant ORCA-IN X 41022988 41022988 deletion of <=200bp A - intron_variant ORCA-IN X 41022988 41022988 deletion of <=200bp A - upstream_gene_variant ORCA-IN X 41025202 41025202 single base substitution C A missense_variant A688E 2063C>A ORCA-IN X 41025202 41025202 single base substitution C A upstream_gene_variant ORCA-IN X 41026737 41026738 deletion of <=200bp CG - exon_variant ORCA-IN X 41026737 41026738 deletion of <=200bp CG - frameshift_variant VV777 ORCA-IN X 41034238 41034238 deletion of <=200bp A - intron_variant ORCA-IN X 41034776 41034776 deletion of <=200bp A - intron_variant ORCA-IN X 41035149 41035149 deletion of <=200bp T - intron_variant ORCA-IN X 41044904 41044904 deletion of <=200bp T - downstream_gene_variant ORCA-IN X 41044904 41044904 deletion of <=200bp T - intron_variant ORCA-IN X 41044904 41044904 deletion of <=200bp T - upstream_gene_variant ORCA-IN X 41046083 41046083 insertion of <=200bp - T downstream_gene_variant ORCA-IN X 41046083 41046083 insertion of <=200bp - T intron_variant ORCA-IN X 41046083 41046083 insertion of <=200bp - T upstream_gene_variant ORCA-IN X 41047083 41047083 deletion of <=200bp T - downstream_gene_variant ORCA-IN X 41047083 41047083 deletion of <=200bp T - intron_variant ORCA-IN X 41047083 41047083 deletion of <=200bp T - upstream_gene_variant ORCA-IN X 41048687 41048687 single base substitution G T downstream_gene_variant ORCA-IN X 41048687 41048687 single base substitution G T exon_variant ORCA-IN X 41048687 41048687 single base substitution G T missense_variant W1312C 3936G>T ORCA-IN X 41056704 41056704 single base substitution C T 3_prime_UTR_variant ORCA-IN X 41056704 41056704 single base substitution C T stop_gained Q1441* 4321C>T ORCA-IN X 41063666 41063666 insertion of <=200bp - T intron_variant ORCA-IN X 41063666 41063666 insertion of <=200bp - T upstream_gene_variant ORCA-IN X 41064765 41064765 single base substitution G C intron_variant ORCA-IN X 41064887 41064887 deletion of <=200bp T - intron_variant ORCA-IN X 41067290 41067290 insertion of <=200bp - T intron_variant ORCA-IN X 41067291 41067291 deletion of <=200bp T - intron_variant ORCA-IN X 41069808 41069808 single base substitution G A exon_variant ORCA-IN X 41069808 41069808 single base substitution G A missense_variant E1688K 5062G>A ORCA-IN X 41073730 41073730 deletion of <=200bp A - downstream_gene_variant ORCA-IN X 41073730 41073730 deletion of <=200bp A - intron_variant ORCA-IN X 41075090 41075090 deletion of <=200bp T - intron_variant ORCA-IN X 41077699 41077699 single base substitution A G missense_variant N2095S 6284A>G ORCA-IN X 41078697 41078697 deletion of <=200bp T - intron_variant ORCA-IN X 41088859 41088859 single base substitution G T exon_variant ORCA-IN X 41088859 41088859 single base substitution G T stop_gained E2420* 7258G>T ORCA-IN X 41091472 41091472 single base substitution T G downstream_gene_variant ORCA-IN X 41091472 41091472 single base substitution T G intron_variant OV-AU X 40941251 40941251 single base substitution G A upstream_gene_variant OV-AU X 40954994 40954994 single base substitution A T intron_variant OV-AU X 40962128 40962128 single base substitution C T intron_variant OV-AU X 40962254 40962254 single base substitution C A intron_variant OV-AU X 40965455 40965455 single base substitution G T intron_variant OV-AU X 40966394 40966394 single base substitution C T intron_variant OV-AU X 40985305 40985305 single base substitution A T intron_variant OV-AU X 40996868 40996868 single base substitution T A intron_variant OV-AU X 41006027 41006027 single base substitution C G intron_variant OV-AU X 41006455 41006455 single base substitution G A intron_variant OV-AU X 41009441 41009441 single base substitution C G intron_variant OV-AU X 41010383 41010383 single base substitution G C intron_variant OV-AU X 41010922 41010922 single base substitution C T intron_variant OV-AU X 41011312 41011312 single base substitution T G intron_variant OV-AU X 41019072 41019072 single base substitution C T intron_variant OV-AU X 41028462 41028462 single base substitution A G downstream_gene_variant OV-AU X 41028462 41028462 single base substitution A G intron_variant OV-AU X 41042134 41042134 single base substitution G C intron_variant OV-AU X 41042134 41042134 single base substitution G C upstream_gene_variant OV-AU X 41044469 41044469 single base substitution C T downstream_gene_variant OV-AU X 41044469 41044469 single base substitution C T intron_variant OV-AU X 41044469 41044469 single base substitution C T upstream_gene_variant OV-AU X 41044478 41044478 single base substitution G C downstream_gene_variant OV-AU X 41044478 41044478 single base substitution G C intron_variant OV-AU X 41044478 41044478 single base substitution G C upstream_gene_variant OV-AU X 41045432 41045432 single base substitution A T downstream_gene_variant OV-AU X 41045432 41045432 single base substitution A T intron_variant OV-AU X 41045432 41045432 single base substitution A T upstream_gene_variant OV-AU X 41054817 41054817 single base substitution C T intron_variant OV-AU X 41054817 41054817 single base substitution C T upstream_gene_variant OV-AU X 41058730 41058730 single base substitution C T downstream_gene_variant OV-AU X 41058730 41058730 single base substitution C T intron_variant OV-AU X 41075482 41075482 deletion of <=200bp A - frameshift_variant N1888 OV-AU X 41075511 41075511 single base substitution G A stop_gained W1897* 5691G>A OV-AU X 41094778 41094778 single base substitution G C 3_prime_UTR_variant OV-AU X 41094778 41094778 single base substitution G C downstream_gene_variant OV-AU X 41098917 41098917 single base substitution C T downstream_gene_variant OV-AU X 41099905 41099905 single base substitution G A downstream_gene_variant OV-AU X 41099906 41099906 single base substitution C T downstream_gene_variant PACA-AU X 40940881 40940881 single base substitution C A upstream_gene_variant PACA-AU X 40940896 40940896 single base substitution A G upstream_gene_variant PACA-AU X 40942028 40942028 single base substitution A G upstream_gene_variant PACA-AU X 40943839 40943839 single base substitution G C upstream_gene_variant PACA-AU X 40943840 40943840 single base substitution C T upstream_gene_variant PACA-AU X 40956637 40956637 single base substitution A C intron_variant PACA-AU X 40959276 40959276 single base substitution G T intron_variant PACA-AU X 40959777 40959777 insertion of <=200bp - T intron_variant PACA-AU X 40963448 40963448 single base substitution T G intron_variant PACA-AU X 40968194 40968194 single base substitution A G intron_variant PACA-AU X 40971759 40971759 single base substitution A T intron_variant PACA-AU X 40972464 40972464 insertion of <=200bp - T intron_variant PACA-AU X 40972617 40972617 single base substitution C T intron_variant PACA-AU X 40988287 40988287 single base substitution C T missense_variant P44L 131C>T PACA-AU X 40994259 40994259 single base substitution G A intron_variant PACA-AU X 41001400 41001400 single base substitution A C intron_variant PACA-AU X 41005217 41005217 single base substitution G T intron_variant PACA-AU X 41007651 41007651 single base substitution A G synonymous_variant Q483Q 1449A>G PACA-AU X 41024100 41024100 single base substitution T C intron_variant PACA-AU X 41024100 41024100 single base substitution T C upstream_gene_variant PACA-AU X 41030814 41030814 insertion of <=200bp - T downstream_gene_variant PACA-AU X 41030814 41030814 insertion of <=200bp - T intron_variant PACA-AU X 41035025 41035025 single base substitution T C intron_variant PACA-AU X 41042637 41042637 single base substitution G T intron_variant PACA-AU X 41042637 41042637 single base substitution G T upstream_gene_variant PACA-AU X 41043721 41043721 single base substitution C G exon_variant PACA-AU X 41043721 41043721 single base substitution C G missense_variant F1117L 3351C>G PACA-AU X 41043721 41043721 single base substitution C G upstream_gene_variant PACA-AU X 41046235 41046235 deletion of <=200bp C - downstream_gene_variant PACA-AU X 41046235 41046235 deletion of <=200bp C - intron_variant PACA-AU X 41046235 41046235 deletion of <=200bp C - upstream_gene_variant PACA-AU X 41053596 41053596 single base substitution T G downstream_gene_variant PACA-AU X 41053596 41053596 single base substitution T G intron_variant PACA-AU X 41053596 41053596 single base substitution T G upstream_gene_variant PACA-AU X 41055019 41055019 single base substitution G T intron_variant PACA-AU X 41055019 41055019 single base substitution G T upstream_gene_variant PACA-AU X 41056806 41056806 single base substitution T C intron_variant PACA-AU X 41066537 41066537 single base substitution C T intron_variant PACA-AU X 41091835 41091835 single base substitution C T 3_prime_UTR_variant PACA-AU X 41091835 41091835 single base substitution C T downstream_gene_variant PACA-AU X 41091860 41091860 single base substitution A C 3_prime_UTR_variant PACA-AU X 41091860 41091860 single base substitution A C downstream_gene_variant PACA-AU X 41091909 41091909 single base substitution C T 3_prime_UTR_variant PACA-AU X 41091909 41091909 single base substitution C T downstream_gene_variant PACA-AU X 41092023 41092023 single base substitution G A 3_prime_UTR_variant PACA-AU X 41092023 41092023 single base substitution G A downstream_gene_variant PACA-AU X 41095844 41095844 single base substitution C T downstream_gene_variant PACA-CA X 40940782 40940782 deletion of <=200bp T - upstream_gene_variant PACA-CA X 40942724 40942724 single base substitution C T upstream_gene_variant PACA-CA X 40948068 40948068 single base substitution C T intron_variant PACA-CA X 40952712 40952712 single base substitution C A intron_variant PACA-CA X 40953400 40953400 single base substitution G A intron_variant PACA-CA X 40959901 40959901 deletion of <=200bp A - intron_variant PACA-CA X 40959909 40959909 deletion of <=200bp T - intron_variant PACA-CA X 40961014 40961014 single base substitution A G intron_variant PACA-CA X 40964926 40964926 single base substitution T C intron_variant PACA-CA X 40968958 40968958 single base substitution T C intron_variant PACA-CA X 40969093 40969093 insertion of <=200bp - TT intron_variant PACA-CA X 40974118 40974118 single base substitution T A intron_variant PACA-CA X 40974588 40974588 single base substitution G A intron_variant PACA-CA X 40975696 40975696 single base substitution C T intron_variant PACA-CA X 40976030 40976030 insertion of <=200bp - T intron_variant PACA-CA X 40976083 40976084 deletion of <=200bp GA - intron_variant PACA-CA X 40977940 40977940 insertion of <=200bp - A intron_variant PACA-CA X 40980801 40980801 single base substitution T C intron_variant PACA-CA X 40991612 40991612 single base substitution A T intron_variant PACA-CA X 40993373 40993373 single base substitution C T intron_variant PACA-CA X 40997371 40997371 single base substitution C T intron_variant PACA-CA X 40999436 40999436 single base substitution A G intron_variant PACA-CA X 41000635 41000635 single base substitution G A missense_variant R371Q 1112G>A PACA-CA X 41007462 41007462 insertion of <=200bp - A intron_variant PACA-CA X 41009081 41009081 single base substitution C T intron_variant PACA-CA X 41010971 41010971 single base substitution C T intron_variant PACA-CA X 41019033 41019033 single base substitution T A intron_variant PACA-CA X 41024845 41024845 single base substitution A G intron_variant PACA-CA X 41024845 41024845 single base substitution A G upstream_gene_variant PACA-CA X 41026491 41026491 single base substitution A C exon_variant PACA-CA X 41026491 41026491 single base substitution A C intron_variant PACA-CA X 41026548 41026548 single base substitution C A exon_variant PACA-CA X 41026548 41026548 single base substitution C A intron_variant PACA-CA X 41031231 41031231 single base substitution G C downstream_gene_variant PACA-CA X 41031231 41031231 single base substitution G C intron_variant PACA-CA X 41033026 41033026 deletion of <=200bp A - intron_variant PACA-CA X 41038489 41038489 insertion of <=200bp - T intron_variant PACA-CA X 41038489 41038489 insertion of <=200bp - T upstream_gene_variant PACA-CA X 41051752 41051752 single base substitution G A downstream_gene_variant PACA-CA X 41051752 41051752 single base substitution G A intron_variant PACA-CA X 41051752 41051752 single base substitution G A upstream_gene_variant PACA-CA X 41054188 41054188 single base substitution A T intron_variant PACA-CA X 41054188 41054188 single base substitution A T upstream_gene_variant PACA-CA X 41059063 41059063 single base substitution G C downstream_gene_variant PACA-CA X 41059063 41059063 single base substitution G C intron_variant PACA-CA X 41064769 41064769 single base substitution T C intron_variant PACA-CA X 41069287 41069287 single base substitution A G intron_variant PACA-CA X 41070720 41070720 single base substitution G A downstream_gene_variant PACA-CA X 41070720 41070720 single base substitution G A intron_variant PACA-CA X 41076516 41076516 single base substitution C T synonymous_variant I2043I 6129C>T PACA-CA X 41077253 41077253 single base substitution A T intron_variant PACA-CA X 41078901 41078901 single base substitution G C intron_variant PACA-CA X 41082424 41082424 single base substitution T A intron_variant PACA-CA X 41087103 41087103 single base substitution G A intron_variant PACA-CA X 41087103 41087103 single base substitution G A upstream_gene_variant PACA-CA X 41088739 41088739 single base substitution G C intron_variant PACA-CA X 41091787 41091787 deletion of <=200bp A - 3_prime_UTR_variant PACA-CA X 41091787 41091787 deletion of <=200bp A - downstream_gene_variant PACA-CA X 41095277 41095277 single base substitution T C 3_prime_UTR_variant PACA-CA X 41095277 41095277 single base substitution T C downstream_gene_variant PACA-CA X 41095334 41095334 single base substitution G A 3_prime_UTR_variant PACA-CA X 41095334 41095334 single base substitution G A downstream_gene_variant PACA-CA X 41096716 41096716 deletion of <=200bp A - downstream_gene_variant PAEN-AU X 40952449 40952449 single base substitution C T intron_variant PAEN-AU X 41005308 41005308 single base substitution A G intron_variant PAEN-IT X 41058062 41058062 single base substitution C T downstream_gene_variant PAEN-IT X 41058062 41058062 single base substitution C T intron_variant PAEN-IT X 41090593 41090593 single base substitution A T downstream_gene_variant PAEN-IT X 41090593 41090593 single base substitution A T intron_variant PAEN-IT X 41100778 41100778 single base substitution A T downstream_gene_variant PBCA-DE X 40939912 40939912 single base substitution C G upstream_gene_variant PBCA-DE X 40941994 40941995 deletion of <=200bp AT - upstream_gene_variant PBCA-DE X 40942022 40942022 single base substitution C G upstream_gene_variant PBCA-DE X 40944301 40944301 single base substitution C G upstream_gene_variant PBCA-DE X 40946885 40946885 insertion of <=200bp - AAACTC intron_variant PBCA-DE X 40947444 40947444 single base substitution G T intron_variant PBCA-DE X 40949327 40949327 insertion of <=200bp - T intron_variant PBCA-DE X 40953490 40953490 single base substitution C T intron_variant PBCA-DE X 40969024 40969024 insertion of <=200bp - G intron_variant PBCA-DE X 41005553 41005553 single base substitution C T intron_variant PBCA-DE X 41031402 41031402 insertion of <=200bp - A downstream_gene_variant PBCA-DE X 41031402 41031402 insertion of <=200bp - A intron_variant PBCA-DE X 41033889 41033889 single base substitution C T intron_variant PBCA-DE X 41035629 41035629 single base substitution C T intron_variant PBCA-DE X 41053423 41053423 single base substitution G T downstream_gene_variant PBCA-DE X 41053423 41053423 single base substitution G T intron_variant PBCA-DE X 41053423 41053423 single base substitution G T upstream_gene_variant PBCA-DE X 41060322 41060322 single base substitution C T downstream_gene_variant PBCA-DE X 41060322 41060322 single base substitution C T missense_variant A1538V 4613C>T PBCA-DE X 41060322 41060322 single base substitution C T upstream_gene_variant PBCA-DE X 41061406 41061406 single base substitution G A downstream_gene_variant PBCA-DE X 41061406 41061406 single base substitution G A intron_variant PBCA-DE X 41061406 41061406 single base substitution G A upstream_gene_variant PBCA-DE X 41070889 41070889 single base substitution C A downstream_gene_variant PBCA-DE X 41070889 41070889 single base substitution C A intron_variant PBCA-DE X 41080662 41080662 single base substitution A G intron_variant PRAD-CA X 40940908 40940908 single base substitution A T upstream_gene_variant PRAD-CA X 40984939 40984939 single base substitution T A intron_variant PRAD-CA X 40998167 40998167 single base substitution C A intron_variant PRAD-CA X 41018791 41018791 single base substitution C T intron_variant PRAD-CA X 41030696 41030696 single base substitution G A downstream_gene_variant PRAD-CA X 41030696 41030696 single base substitution G A intron_variant PRAD-CA X 41034891 41034891 single base substitution G C intron_variant PRAD-CA X 41038211 41038211 single base substitution A T intron_variant PRAD-CA X 41039723 41039723 single base substitution A C intron_variant PRAD-CA X 41039723 41039723 single base substitution A C upstream_gene_variant PRAD-CA X 41045842 41045842 single base substitution G T downstream_gene_variant PRAD-CA X 41045842 41045842 single base substitution G T stop_gained E1211* 3631G>T PRAD-CA X 41045842 41045842 single base substitution G T upstream_gene_variant PRAD-CA X 41052841 41052841 single base substitution G A downstream_gene_variant PRAD-CA X 41052841 41052841 single base substitution G A intron_variant PRAD-CA X 41052841 41052841 single base substitution G A upstream_gene_variant PRAD-CA X 41073897 41073897 single base substitution C T downstream_gene_variant PRAD-CA X 41073897 41073897 single base substitution C T stop_gained Q1756* 5266C>T PRAD-CA X 41078437 41078437 single base substitution G A missense_variant R2173H 6518G>A PRAD-UK X 40985067 40985073 deletion of <=200bp GATAATT - intron_variant PRAD-UK X 40997847 40997847 single base substitution C T intron_variant PRAD-UK X 41002755 41002755 single base substitution G A intron_variant PRAD-UK X 41003490 41003490 single base substitution T G intron_variant PRAD-UK X 41034152 41034152 single base substitution G A intron_variant PRAD-UK X 41042057 41042057 single base substitution A G intron_variant PRAD-UK X 41042057 41042057 single base substitution A G upstream_gene_variant PRAD-UK X 41048671 41048671 single base substitution G A downstream_gene_variant PRAD-UK X 41048671 41048671 single base substitution G A exon_variant PRAD-UK X 41048671 41048671 single base substitution G A missense_variant S1307N 3920G>A PRAD-UK X 41068253 41068253 single base substitution G A intron_variant PRAD-UK X 41077362 41077362 single base substitution G T intron_variant PRAD-UK X 41080149 41080149 single base substitution A G intron_variant PRAD-UK X 41097981 41097981 single base substitution C G downstream_gene_variant PRAD-US X 40999970 40999970 single base substitution A G missense_variant D239G 716A>G PRAD-US X 41000651 41000651 single base substitution G A synonymous_variant E376E 1128G>A READ-US X 41056658 41056658 single base substitution G T 3_prime_UTR_variant READ-US X 41056658 41056658 single base substitution G T synonymous_variant T1425T 4275G>T READ-US X 41075414 41075414 single base substitution T G missense_variant L1865R 5594T>G RECA-EU X 41000936 41000936 single base substitution T G intron_variant RECA-EU X 41012067 41012067 single base substitution T C intron_variant RECA-EU X 41029375 41029375 single base substitution C T downstream_gene_variant RECA-EU X 41029375 41029375 single base substitution C T missense_variant R922C 2764C>T RECA-EU X 41035970 41035970 single base substitution A G intron_variant RECA-EU X 41058308 41058308 single base substitution A T downstream_gene_variant RECA-EU X 41058308 41058308 single base substitution A T intron_variant RECA-EU X 41065822 41065822 single base substitution T C intron_variant RECA-EU X 41074221 41074221 single base substitution C A downstream_gene_variant RECA-EU X 41074221 41074221 single base substitution C A intron_variant RECA-EU X 41075936 41075936 single base substitution A T intron_variant RECA-EU X 41086253 41086253 single base substitution A T intron_variant RECA-EU X 41086253 41086253 single base substitution A T upstream_gene_variant RECA-EU X 41088688 41088688 single base substitution G T intron_variant RECA-EU X 41091985 41091985 single base substitution G T 3_prime_UTR_variant RECA-EU X 41091985 41091985 single base substitution G T downstream_gene_variant SKCA-BR X 40940416 40940416 single base substitution A G upstream_gene_variant SKCA-BR X 40944160 40944160 single base substitution A C upstream_gene_variant SKCA-BR X 40944683 40944683 insertion of <=200bp - GT upstream_gene_variant SKCA-BR X 40952160 40952160 single base substitution C T intron_variant SKCA-BR X 40963354 40963354 single base substitution C T intron_variant SKCA-BR X 40967703 40967703 single base substitution T G intron_variant SKCA-BR X 40972385 40972385 single base substitution C T intron_variant SKCA-BR X 40979337 40979350 deletion of <=200bp AAAACTTTGTTTTG - intron_variant SKCA-BR X 40989481 40989481 single base substitution G A intron_variant SKCA-BR X 40989687 40989687 single base substitution G A intron_variant SKCA-BR X 40989752 40989753 deletion of <=200bp GT - intron_variant SKCA-BR X 40989990 40989990 single base substitution T C intron_variant SKCA-BR X 40991337 40991337 single base substitution C T intron_variant SKCA-BR X 40996265 40996265 single base substitution G C missense_variant R215P 644G>C SKCA-BR X 41005936 41005938 deletion of <=200bp TTG - intron_variant SKCA-BR X 41005953 41005953 single base substitution C T intron_variant SKCA-BR X 41005960 41005960 single base substitution T C intron_variant SKCA-BR X 41008485 41008485 single base substitution G T intron_variant SKCA-BR X 41029805 41029805 single base substitution C T downstream_gene_variant SKCA-BR X 41029805 41029805 single base substitution C T missense_variant P987L 2960C>T SKCA-BR X 41035113 41035113 single base substitution G A intron_variant SKCA-BR X 41035850 41035850 single base substitution C T intron_variant SKCA-BR X 41041188 41041188 single base substitution A T intron_variant SKCA-BR X 41041188 41041188 single base substitution A T upstream_gene_variant SKCA-BR X 41051828 41051828 single base substitution T C downstream_gene_variant SKCA-BR X 41051828 41051828 single base substitution T C intron_variant SKCA-BR X 41051828 41051828 single base substitution T C upstream_gene_variant SKCA-BR X 41052398 41052398 single base substitution A G downstream_gene_variant SKCA-BR X 41052398 41052398 single base substitution A G intron_variant SKCA-BR X 41052398 41052398 single base substitution A G upstream_gene_variant SKCA-BR X 41052416 41052416 single base substitution A G downstream_gene_variant SKCA-BR X 41052416 41052416 single base substitution A G intron_variant SKCA-BR X 41052416 41052416 single base substitution A G upstream_gene_variant SKCA-BR X 41056326 41056326 single base substitution T A intron_variant SKCA-BR X 41062600 41062600 single base substitution C T downstream_gene_variant SKCA-BR X 41062600 41062600 single base substitution C T intron_variant SKCA-BR X 41062600 41062600 single base substitution C T upstream_gene_variant SKCA-BR X 41062601 41062601 single base substitution C T downstream_gene_variant SKCA-BR X 41062601 41062601 single base substitution C T intron_variant SKCA-BR X 41062601 41062601 single base substitution C T upstream_gene_variant SKCA-BR X 41065503 41065503 single base substitution A T intron_variant SKCA-BR X 41067049 41067049 single base substitution C T intron_variant SKCA-BR X 41069856 41069856 single base substitution T G exon_variant SKCA-BR X 41069856 41069856 single base substitution T G missense_variant L1704V 5110T>G SKCA-BR X 41069896 41069896 single base substitution C T exon_variant SKCA-BR X 41069896 41069896 single base substitution C T missense_variant S1717F 5150C>T SKCA-BR X 41070193 41070193 single base substitution C T downstream_gene_variant SKCA-BR X 41070193 41070193 single base substitution C T intron_variant SKCA-BR X 41071065 41071065 single base substitution A C downstream_gene_variant SKCA-BR X 41071065 41071065 single base substitution A C intron_variant SKCA-BR X 41071729 41071729 single base substitution G A downstream_gene_variant SKCA-BR X 41071729 41071729 single base substitution G A intron_variant SKCA-BR X 41075052 41075052 single base substitution C T intron_variant SKCA-BR X 41087349 41087349 single base substitution C T intron_variant SKCA-BR X 41087349 41087349 single base substitution C T upstream_gene_variant SKCA-BR X 41091985 41091985 single base substitution G A 3_prime_UTR_variant SKCA-BR X 41091985 41091985 single base substitution G A downstream_gene_variant SKCA-BR X 41093298 41093298 insertion of <=200bp - CT 3_prime_UTR_variant SKCA-BR X 41093298 41093298 insertion of <=200bp - CT downstream_gene_variant SKCA-BR X 41098917 41098917 single base substitution C T downstream_gene_variant SKCA-BR X 41099339 41099339 single base substitution T G downstream_gene_variant SKCM-US X 40982966 40982966 single base substitution C T stop_gained Q29* 85C>T SKCM-US X 40982969 40982969 single base substitution C T stop_gained Q30* 88C>T SKCM-US X 41000634 41000634 single base substitution C T stop_gained R371* 1111C>T SKCM-US X 41007791 41007791 single base substitution G A missense_variant S530N 1589G>A SKCM-US X 41010280 41010283 deletion of <=200bp GTTT - frameshift_variant SL578 SKCM-US X 41029282 41029282 single base substitution C T downstream_gene_variant SKCM-US X 41029282 41029282 single base substitution C T stop_gained R891* 2671C>T SKCM-US X 41029487 41029487 single base substitution C T downstream_gene_variant SKCM-US X 41029487 41029487 single base substitution C T missense_variant S959L 2876C>T SKCM-US X 41043842 41043842 single base substitution T C exon_variant SKCM-US X 41043842 41043842 single base substitution T C synonymous_variant L1158L 3472T>C SKCM-US X 41043842 41043842 single base substitution T C upstream_gene_variant SKCM-US X 41043859 41043859 single base substitution C T exon_variant SKCM-US X 41043859 41043859 single base substitution C T synonymous_variant G1163G 3489C>T SKCM-US X 41043859 41043859 single base substitution C T upstream_gene_variant SKCM-US X 41045827 41045827 single base substitution C T downstream_gene_variant SKCM-US X 41045827 41045827 single base substitution C T missense_variant P1206S 3616C>T SKCM-US X 41045827 41045827 single base substitution C T upstream_gene_variant SKCM-US X 41048638 41048638 single base substitution T C downstream_gene_variant SKCM-US X 41048638 41048638 single base substitution T C exon_variant SKCM-US X 41048638 41048638 single base substitution T C missense_variant F1296S 3887T>C SKCM-US X 41055511 41055511 single base substitution C T exon_variant SKCM-US X 41055511 41055511 single base substitution C T missense_variant R1329C 3985C>T SKCM-US X 41055614 41055614 single base substitution T G splice_donor_variant SKCM-US X 41057871 41057871 single base substitution G A downstream_gene_variant SKCM-US X 41057871 41057871 single base substitution G A missense_variant V1491I 4471G>A SKCM-US X 41069821 41069821 single base substitution C T exon_variant SKCM-US X 41069821 41069821 single base substitution C T missense_variant S1692L 5075C>T SKCM-US X 41075159 41075159 single base substitution C T missense_variant T1780I 5339C>T SKCM-US X 41075484 41075484 single base substitution T C synonymous_variant N1888N 5664T>C SKCM-US X 41075851 41075851 single base substitution C T stop_gained Q2011* 6031C>T SKCM-US X 41084153 41084153 single base substitution C T missense_variant R2304C 6910C>T SKCM-US X 41084153 41084153 single base substitution C T upstream_gene_variant SKCM-US X 41088904 41088904 single base substitution C T exon_variant SKCM-US X 41088904 41088904 single base substitution C T missense_variant P2435S 7303C>T STAD-US X 40982957 40982957 deletion of <=200bp C - frameshift_variant P26 STAD-US X 40994031 40994031 single base substitution A C missense_variant I126L 376A>C STAD-US X 40996215 40996215 single base substitution A G synonymous_variant S198S 594A>G STAD-US X 41000004 41000004 single base substitution A G synonymous_variant Q250Q 750A>G STAD-US X 41000424 41000424 single base substitution G T stop_gained E326* 976G>T STAD-US X 41000617 41000617 single base substitution T C missense_variant V365A 1094T>C STAD-US X 41002634 41002634 single base substitution C T missense_variant R418C 1252C>T STAD-US X 41012336 41012336 single base substitution T C splice_donor_variant STAD-US X 41025133 41025133 single base substitution T C missense_variant L665S 1994T>C STAD-US X 41025133 41025133 single base substitution T C upstream_gene_variant STAD-US X 41025387 41025387 single base substitution C T stop_gained R750* 2248C>T STAD-US X 41025387 41025387 single base substitution C T upstream_gene_variant STAD-US X 41027344 41027344 single base substitution A G exon_variant STAD-US X 41027344 41027344 single base substitution A G missense_variant K837E 2509A>G STAD-US X 41027442 41027442 single base substitution T C exon_variant STAD-US X 41027442 41027442 single base substitution T C synonymous_variant H869H 2607T>C STAD-US X 41029259 41029259 single base substitution G C downstream_gene_variant STAD-US X 41029259 41029259 single base substitution G C missense_variant G883A 2648G>C STAD-US X 41043383 41043383 single base substitution T C splice_donor_variant STAD-US X 41043383 41043383 single base substitution T C upstream_gene_variant STAD-US X 41045867 41045867 single base substitution T C downstream_gene_variant STAD-US X 41045867 41045867 single base substitution T C missense_variant V1219A 3656T>C STAD-US X 41045867 41045867 single base substitution T C upstream_gene_variant STAD-US X 41055854 41055855 deletion of <=200bp AG - 3_prime_UTR_variant STAD-US X 41055854 41055855 deletion of <=200bp AG - frameshift_variant R1366 STAD-US X 41060361 41060361 single base substitution G A downstream_gene_variant STAD-US X 41060361 41060361 single base substitution G A missense_variant R1551H 4652G>A STAD-US X 41060361 41060361 single base substitution G A upstream_gene_variant STAD-US X 41060495 41060497 deletion of <=200bp GAT - downstream_gene_variant STAD-US X 41060495 41060497 deletion of <=200bp GAT - inframe_deletion D1596 STAD-US X 41060495 41060497 deletion of <=200bp GAT - upstream_gene_variant STAD-US X 41064672 41064672 single base substitution T C exon_variant STAD-US X 41064672 41064672 single base substitution T C synonymous_variant L1647L 4941T>C STAD-US X 41069787 41069787 single base substitution C T exon_variant STAD-US X 41069787 41069787 single base substitution C T missense_variant R1681C 5041C>T STAD-US X 41069826 41069826 single base substitution G A exon_variant STAD-US X 41069826 41069826 single base substitution G A missense_variant V1694M 5080G>A STAD-US X 41075642 41075642 single base substitution G A missense_variant R1941H 5822G>A STAD-US X 41075795 41075795 single base substitution G A missense_variant R1992Q 5975G>A STAD-US X 41077761 41077761 single base substitution T C missense_variant F2116L 6346T>C STAD-US X 41082472 41082472 single base substitution G A missense_variant V2190M 6568G>A STAD-US X 41089035 41089035 insertion of <=200bp - A exon_variant STAD-US X 41089035 41089035 insertion of <=200bp - A frameshift_variant V2478V? STAD-US X 41089035 41089035 insertion of <=200bp - A splice_region_variant STAD-US X 41089041 41089041 single base substitution A G exon_variant STAD-US X 41089041 41089041 single base substitution A G intron_variant STAD-US X 41089041 41089041 single base substitution A G synonymous_variant K2480K 7440A>G THCA-SA X 41084060 41084060 single base substitution C T stop_gained Q2273* 6817C>T THCA-SA X 41084060 41084060 single base substitution C T upstream_gene_variant THCA-SA X 41092664 41092664 single base substitution G A 3_prime_UTR_variant THCA-SA X 41092664 41092664 single base substitution G A downstream_gene_variant THCA-US X 40988337 40988337 single base substitution G T stop_gained E61* 181G>T THCA-US X 41043681 41043681 insertion of <=200bp - A exon_variant THCA-US X 41043681 41043681 insertion of <=200bp - A frameshift_variant A1104D? THCA-US X 41043681 41043681 insertion of <=200bp - A upstream_gene_variant THCA-US X 41058005 41058005 single base substitution T C downstream_gene_variant THCA-US X 41058005 41058005 single base substitution T C splice_donor_variant THCA-US X 41073950 41073950 single base substitution A G downstream_gene_variant THCA-US X 41073950 41073950 single base substitution A G synonymous_variant K1773K 5319A>G THCA-US X 41075213 41075213 single base substitution A C missense_variant K1798T 5393A>C UCEC-US X 40988333 40988333 single base substitution G A synonymous_variant Q59Q 177G>A UCEC-US X 40990752 40990752 single base substitution A G synonymous_variant E95E 285A>G UCEC-US X 40994075 40994075 single base substitution G A stop_gained W140* 420G>A UCEC-US X 40996172 40996172 single base substitution T G missense_variant F184C 551T>G UCEC-US X 40996173 40996173 single base substitution C A missense_variant F184L 552C>A UCEC-US X 40996188 40996188 single base substitution T A synonymous_variant G189G 567T>A UCEC-US X 40996249 40996249 single base substitution C G missense_variant R210G 628C>G UCEC-US X 40999934 40999934 single base substitution A C missense_variant K227T 680A>C UCEC-US X 41000333 41000333 single base substitution A C missense_variant K295N 885A>C UCEC-US X 41002634 41002634 single base substitution C T missense_variant R418C 1252C>T UCEC-US X 41002675 41002675 single base substitution T C synonymous_variant L431L 1293T>C UCEC-US X 41003881 41003881 single base substitution T G splice_donor_variant UCEC-US X 41007709 41007709 single base substitution A G missense_variant M503V 1507A>G UCEC-US X 41010204 41010204 single base substitution G T missense_variant D553Y 1657G>T UCEC-US X 41012233 41012233 single base substitution G A missense_variant R599H 1796G>A UCEC-US X 41012294 41012294 single base substitution C T synonymous_variant N619N 1857C>T UCEC-US X 41025143 41025143 single base substitution T C synonymous_variant G668G 2004T>C UCEC-US X 41025143 41025143 single base substitution T C upstream_gene_variant UCEC-US X 41026800 41026800 single base substitution G T exon_variant UCEC-US X 41026800 41026800 single base substitution G T synonymous_variant T798T 2394G>T UCEC-US X 41027380 41027380 single base substitution C T exon_variant UCEC-US X 41027380 41027380 single base substitution C T stop_gained R849* 2545C>T UCEC-US X 41029255 41029255 single base substitution C T downstream_gene_variant UCEC-US X 41029255 41029255 single base substitution C T missense_variant R882C 2644C>T UCEC-US X 41029342 41029342 single base substitution A G downstream_gene_variant UCEC-US X 41029342 41029342 single base substitution A G missense_variant T911A 2731A>G UCEC-US X 41029422 41029422 single base substitution C T downstream_gene_variant UCEC-US X 41029422 41029422 single base substitution C T synonymous_variant G937G 2811C>T UCEC-US X 41029487 41029487 single base substitution C T downstream_gene_variant UCEC-US X 41029487 41029487 single base substitution C T missense_variant S959L 2876C>T UCEC-US X 41031196 41031196 single base substitution A G downstream_gene_variant UCEC-US X 41031196 41031196 single base substitution A G missense_variant K1045E 3133A>G UCEC-US X 41031207 41031207 single base substitution G A downstream_gene_variant UCEC-US X 41031207 41031207 single base substitution G A synonymous_variant P1048P 3144G>A UCEC-US X 41043261 41043261 single base substitution G A exon_variant UCEC-US X 41043261 41043261 single base substitution G A synonymous_variant T1053T 3159G>A UCEC-US X 41043261 41043261 single base substitution G A upstream_gene_variant UCEC-US X 41043675 41043675 single base substitution C T exon_variant UCEC-US X 41043675 41043675 single base substitution C T missense_variant A1102V 3305C>T UCEC-US X 41043675 41043675 single base substitution C T upstream_gene_variant UCEC-US X 41043909 41043910 deletion of <=200bp GT - exon_variant UCEC-US X 41043909 41043910 deletion of <=200bp GT - frameshift_variant G1180 UCEC-US X 41043909 41043910 deletion of <=200bp GT - upstream_gene_variant UCEC-US X 41047318 41047318 single base substitution C T downstream_gene_variant UCEC-US X 41047318 41047318 single base substitution C T missense_variant S1253L 3758C>T UCEC-US X 41047318 41047318 single base substitution C T upstream_gene_variant UCEC-US X 41055531 41055531 single base substitution G A exon_variant UCEC-US X 41055531 41055531 single base substitution G A synonymous_variant Q1335Q 4005G>A UCEC-US X 41055854 41055855 deletion of <=200bp AG - 3_prime_UTR_variant UCEC-US X 41055854 41055855 deletion of <=200bp AG - frameshift_variant R1366 UCEC-US X 41055877 41055877 single base substitution C T 3_prime_UTR_variant UCEC-US X 41055877 41055877 single base substitution C T synonymous_variant G1373G 4119C>T UCEC-US X 41057933 41057933 single base substitution C T downstream_gene_variant UCEC-US X 41057933 41057933 single base substitution C T synonymous_variant G1511G 4533C>T UCEC-US X 41057991 41057991 single base substitution A G downstream_gene_variant UCEC-US X 41057991 41057991 single base substitution A G missense_variant T1531A 4591A>G UCEC-US X 41060377 41060377 single base substitution C T downstream_gene_variant UCEC-US X 41060377 41060377 single base substitution C T synonymous_variant F1556F 4668C>T UCEC-US X 41060377 41060377 single base substitution C T upstream_gene_variant UCEC-US X 41060457 41060457 single base substitution A G downstream_gene_variant UCEC-US X 41060457 41060457 single base substitution A G missense_variant N1583S 4748A>G UCEC-US X 41060457 41060457 single base substitution A G upstream_gene_variant UCEC-US X 41060463 41060465 deletion of <=200bp TTC - downstream_gene_variant UCEC-US X 41060463 41060465 deletion of <=200bp TTC - inframe_deletion IL1585I UCEC-US X 41060463 41060465 deletion of <=200bp TTC - upstream_gene_variant UCEC-US X 41073894 41073894 single base substitution G A downstream_gene_variant UCEC-US X 41073894 41073894 single base substitution G A missense_variant E1755K 5263G>A UCEC-US X 41073934 41073934 single base substitution C T downstream_gene_variant UCEC-US X 41073934 41073934 single base substitution C T missense_variant A1768V 5303C>T UCEC-US X 41073963 41073963 single base substitution G A downstream_gene_variant UCEC-US X 41073963 41073963 single base substitution G A splice_donor_variant UCEC-US X 41075316 41075316 single base substitution C T synonymous_variant V1832V 5496C>T UCEC-US X 41075375 41075375 single base substitution A C missense_variant Q1852P 5555A>C UCEC-US X 41075689 41075689 single base substitution G A missense_variant D1957N 5869G>A UCEC-US X 41075904 41075904 single base substitution C T splice_region_variant UCEC-US X 41076540 41076540 single base substitution C A missense_variant F2051L 6153C>A UCEC-US X 41077651 41077651 single base substitution G A missense_variant R2079H 6236G>A UCEC-US X 41077684 41077684 single base substitution A G missense_variant H2090R 6269A>G UCEC-US X 41077839 41077839 single base substitution C T missense_variant P2142S 6424C>T UCEC-US X 41078377 41078377 single base substitution G A missense_variant S2153N 6458G>A UCEC-US X 41084093 41084093 single base substitution A C missense_variant S2284R 6850A>C UCEC-US X 41084093 41084093 single base substitution A C upstream_gene_variant UCEC-US X 41084140 41084140 single base substitution C T synonymous_variant T2299T 6897C>T UCEC-US X 41084140 41084140 single base substitution C T upstream_gene_variant UCEC-US X 41084336 41084336 insertion of <=200bp - T frameshift_variant Y2336L? UCEC-US X 41084336 41084336 insertion of <=200bp - T upstream_gene_variant UCEC-US X 41089023 41089023 single base substitution T C exon_variant UCEC-US X 41089023 41089023 single base substitution T C synonymous_variant C2474C 7422T>C UCEC-US X 41089043 41089043 single base substitution C T exon_variant UCEC-US X 41089043 41089043 single base substitution C T intron_variant UCEC-US X 41089043 41089043 single base substitution C T missense_variant A2481V 7442C>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand RK269_C01 COSM3701850 c.906C>A p.A302A Substitution - coding silent 23:41141101-41141101 + CHC2113T COSM5347538 c.1040_1055del16 p.A347fs*3 Deletion - Frameshift 23:41141331-41141346 + TCGA-AA-3492-01 COSM1467964 c.4073T>C p.F1358S Substitution - Missense 23:41196346-41196346 + TL67 COSM5752011 c.6614_6615insAGCGCC p.F2205>LAP Complex - insertion inframe 23:41223265-41223266 + Pat_46_A COSM5877852 c.6758G>A p.G2253D Substitution - Missense 23:41224769-41224769 + RK269_C01 COSM3701851 c.885C>A p.A295A Substitution - coding silent 23:41141101-41141101 + TCGA-AP-A0LL-01 COSM1121365 c.6318G>T p.R2106S Substitution - Missense 23:41218501-41218501 + TCGA-DB-A64L-01 COSM3973662 c.5419G>A p.D1807N Substitution - Missense 23:41216007-41216007 + TCGA-A5-A0GP-01 COSM1599403 c.3133A>G p.K1045E Substitution - Missense 23:41171943-41171943 + TCGA-66-2786-01 COSM757273 c.5934A>T p.S1978S Substitution - coding silent 23:41216522-41216522 + C086 COSM5541504 c.142C>T p.P48S Substitution - Missense 23:41129045-41129045 + 420 COSM4432129 c.2416G>T p.E806* Substitution - Nonsense 23:41168019-41168019 + EGC15 COSM5064691 c.2758G>A p.V920I Substitution - Missense 23:41170137-41170137 + PD11367a COSM5752167 c.4527_4530delCAAA p.Q1511fs*1 Deletion - Frameshift 23:41198695-41198698 + EWS502 COSM4589424 c.5415C>T p.F1805F Substitution - coding silent 23:41216003-41216003 + AML14 COSM166875 c.1728G>A p.A576A Substitution - coding silent 23:41151043-41151043 + 308_T COSM3965249 c.2728G>A p.D910N Substitution - Missense 23:41170086-41170086 + TCGA-AP-A0LM-01 COSM1121350 c.4570A>G p.T1524A Substitution - Missense 23:41198738-41198738 + TCGA-AP-A051-01 COSM1599413 c.1293T>C p.L431L Substitution - coding silent 23:41143422-41143422 + TCGA-B5-A0JR-01 COSM1599400 c.3539_3540delGT p.V1181fs*12 Deletion - Frameshift 23:41184656-41184657 + TCGA-B0-5705-01 COSM488365 c.452A>G p.N151S Substitution - Missense 23:41136820-41136820 + BK0047D COSM4187866 c.157C>T p.Q53* Substitution - Nonsense 23:41129060-41129060 + TCGA-A5-A0GH-01 COSM1599392 c.4754_4756delTTC p.L1586delL Deletion - In frame 23:41201210-41201212 + TCGA-ER-A198-06 COSM3561669 c.88C>T p.Q30* Substitution - Nonsense 23:41123716-41123716 + PD4203a COSM165460 c.6214C>T p.R2072C Substitution - Missense 23:41218397-41218397 + TCGA-D1-A16F-01 COSM1599395 c.4533C>T p.G1511G Substitution - coding silent 23:41198680-41198680 + TCGA-DU-6410-01 COSM3973659 c.4388T>C p.I1463T Substitution - Missense 23:41198535-41198535 + TCGA-D3-A51G-06 COSM3561679 c.3489C>T p.G1163G Substitution - coding silent 23:41184606-41184606 + ccRCC-27 COSM1664932 c.1159G>T p.A387S Substitution - Missense 23:41141429-41141429 + S00944 COSM316426 c.2094G>A p.M698I Substitution - Missense 23:41166001-41166001 + TCGA-B5-A11E-01 COSM1599390 c.5331+1G>A p.? Unknown 23:41214710-41214710 + TCGA-A5-A0GW-01 COSM1121352 c.4727A>G p.N1576S Substitution - Missense 23:41201204-41201204 + C547 COSM1121335 c.2623C>T p.R875C Substitution - Missense 23:41170002-41170002 + 401 COSM4429726 c.5746A>T p.M1916L Substitution - Missense 23:41216313-41216313 + PT49 COSM5936826 c.6794C>T p.S2265L Substitution - Missense 23:41224784-41224784 + TCGA-EM-A1CV-01 COSM3372265 c.5298A>G p.K1766K Substitution - coding silent 23:41214697-41214697 + HCC084T COSM3844698 c.3873G>C p.L1291F Substitution - Missense 23:41189392-41189392 + S01567 COSM4386729 c.198_199insT p.P68fs*4 Insertion - Frameshift 23:41129101-41129102 + 1T COSM1636541 c.6284A>G p.N2095S Substitution - Missense 23:41218446-41218446 + TCGA-EE-A2MF-06 COSM1121338 c.2855C>T p.S952L Substitution - Missense 23:41170234-41170234 + PD6412a COSM5752394 c.3259-2_3260delAGGT p.? Unknown 23:41184395-41184398 + TCGA-D7-8579-01 COSM1121326 c.1231C>T p.R411C Substitution - Missense 23:41143381-41143381 + p2_VII-2 COSM1738291 c.7033A>C p.T2345P Substitution - Missense 23:41225130-41225130 + PTC-88C COSM4156843 c.6723C>A p.V2241V Substitution - coding silent 23:41223374-41223374 + TCGA-C8-A26Y-01 COSM3844693 c.3805G>C p.E1269Q Substitution - Missense 23:41188112-41188112 + tumor_4133263 COSM5947822 c.6330A>G p.A2110A Substitution - coding silent 23:41218513-41218513 + pfg043T COSM4753529 c.3162T>G p.C1054W Substitution - Missense 23:41184032-41184032 + p2_VII-1 COSM1738290 c.7054A>C p.T2352P Substitution - Missense 23:41225130-41225130 + TCGA-EE-A3J7-06 COSM3913993 c.85C>T p.Q29* Substitution - Nonsense 23:41123713-41123713 + TCGA-CA-6718-01 COSM1467971 c.4952G>A p.R1651Q Substitution - Missense 23:41205451-41205451 + TCGA-CG-5721-01 COSM4109459 c.376A>C p.I126L Substitution - Missense 23:41134778-41134778 + TCGA-CM-5864-01 COSM1467968 c.4439A>C p.N1480T Substitution - Missense 23:41198586-41198586 + 9583_CLM COSM5757542 c.7096C>T p.R2366* Substitution - Nonsense 23:41229287-41229287 + LUAD-CHTN-MAD06-00668 COSM360604 c.283G>T p.E95* Substitution - Nonsense 23:41131497-41131497 + TCGA-CM-5864-01 COSM1467966 c.4220T>G p.L1407R Substitution - Missense 23:41196725-41196725 + 07-058 COSM3736499 c.1846T>C p.Y616H Substitution - Missense 23:41153051-41153051 + TCGA-AN-A046-01 COSM3844691 c.1644G>T p.K548N Substitution - Missense 23:41150938-41150938 + ESCC_BICR_041T COSM5441470 c.1315G>A p.V439M Substitution - Missense 23:41144543-41144543 + DM79 COSM5611153 c.7191C>T p.I2397I Substitution - coding silent 23:41229403-41229403 + 9-RS COSM1731894 c.6193G>T p.G2065C Substitution - Missense 23:41217327-41217327 + PD8617a COSM5752444 c.419delG p.W140fs*1 Deletion - Frameshift 23:41134821-41134821 + 2215529 COSM612949 c.4994G>T p.R1665M Substitution - Missense 23:41205493-41205493 + TCGA-BP-4160-01 COSM3364001 c.3693A>G p.R1231R Substitution - coding silent 23:41188000-41188000 + RK131_C01 COSM3701852 c.1985+10A>G p.? Unknown 23:41162887-41162887 + RK176_C01 COSM3766943 c.7351G>T p.E2451* Substitution - Nonsense 23:41229720-41229720 + TCGA-A6-6650-01 COSM3694584 c.5553G>T p.E1851D Substitution - Missense 23:41216120-41216120 + TCGA-AZ-4315-01 COSM1467999 c.7626G>T p.M2542I Substitution - Missense 23:41232437-41232437 + OSCC-GB_00460111 COSM3713951 c.7258G>T p.E2420* Substitution - Nonsense 23:41229606-41229606 + HCT8 COSM4635808 c.694G>A p.D232N Substitution - Missense 23:41140716-41140716 + S02384 COSM5698678 c.6820G>T p.V2274L Substitution - Missense 23:41224831-41224831 + TCGA-A3-3387-01 COSM488368 c.6755T>C p.F2252S Substitution - Missense 23:41224766-41224766 + TCGA-BR-6563-01 COSM4109479 c.3258+2T>C p.? Unknown 23:41184130-41184130 + TCGA-EM-A4FM-01 COSM3372263 c.4582+2T>C p.? Unknown 23:41198752-41198752 + TCGA-DK-A3X1-01 COSM3800597 c.1657G>C p.D553H Substitution - Missense 23:41150951-41150951 + TCGA-BS-A0UF-01 COSM1599415 c.885A>C p.K295N Substitution - Missense 23:41141080-41141080 + SC_9081 COSM5547221 c.316delA p.K107fs*18 Deletion - Frameshift 23:41131530-41131530 + HCC125T COSM1625889 c.4343G>A p.G1448D Substitution - Missense 23:41197494-41197494 + p2_III-1 COSM1738291 c.7033A>C p.T2345P Substitution - Missense 23:41225130-41225130 + 8044642 COSM3390635 c.3351C>G p.F1117L Substitution - Missense 23:41184468-41184468 + 8031556 COSM3390632 c.131C>T p.P44L Substitution - Missense 23:41129034-41129034 + 1T COSM1636542 c.6263A>G p.N2088S Substitution - Missense 23:41218446-41218446 + TCGA-BS-A0UF-01 COSM1121359 c.5534A>C p.Q1845P Substitution - Missense 23:41216122-41216122 + 587376 COSM1232131 c.1091G>A p.R364Q Substitution - Missense 23:41141382-41141382 + TCGA-AP-A056-01 COSM1599419 c.551T>G p.F184C Substitution - Missense 23:41136919-41136919 + OSCC-GB_00460111 COSM3713952 c.7237G>T p.E2413* Substitution - Nonsense 23:41229606-41229606 + 27 COSM5748849 c.4051_4052insCTTTT p.L1351fs*31 Insertion - Frameshift 23:41196324-41196325 + MDA-N COSM1682560 c.965C>T p.P322L Substitution - Missense 23:41141160-41141160 + SJHGG053_A COSM187984 c.2524C>T p.R842* Substitution - Nonsense 23:41168127-41168127 + p2_II-2 COSM1738290 c.7054A>C p.T2352P Substitution - Missense 23:41225130-41225130 + TCGA-AX-A0J0-01 COSM1121361 c.6063C>T p.P2021P Substitution - coding silent 23:41216651-41216651 + 087T COSM1731217 c.2161G>T p.E721* Substitution - Nonsense 23:41166047-41166047 + TCGA-HC-8257-01 COSM4393676 c.716A>G p.D239G Substitution - Missense 23:41140717-41140717 + WT028 COSM1599396 c.4119C>T p.G1373G Substitution - coding silent 23:41196624-41196624 + TCGA-B9-A69E-01 COSM3992479 c.3419C>T p.A1140V Substitution - Missense 23:41184557-41184557 + TCGA-B5-A11E-01 COSM1599421 c.177G>A p.Q59Q Substitution - coding silent 23:41129080-41129080 + Karpas-1106P COSM2964867 c.4892G>A p.S1631N Substitution - Missense 23:41205370-41205370 + TCGA-BR-6563-01 COSM4109478 c.3279+2T>C p.? Unknown 23:41184130-41184130 + C0085T COSM4154952 c.2764C>T p.R922C Substitution - Missense 23:41170122-41170122 + CHC1603T COSM4801831 c.4150A>G p.I1384V Substitution - Missense 23:41196676-41196676 + TCGA-D1-A165-01 COSM1155371 c.3054C>T p.I1018I Substitution - coding silent 23:41171864-41171864 + S00944 COSM316426 c.2094G>A p.M698I Substitution - Missense 23:41166001-41166001 + TCGA-HC-8257-01 COSM4393677 c.695A>G p.D232G Substitution - Missense 23:41140717-41140717 + T2944 COSM4739961 c.4260G>A p.T1420T Substitution - coding silent 23:41197390-41197390 + TCGA-BS-A0UV-01 COSM1599393 c.4668C>T p.F1556F Substitution - coding silent 23:41201124-41201124 + PTC_449 COSM5960096 c.6817C>T p.Q2273* Substitution - Nonsense 23:41224807-41224807 + ccRCC-23 COSM1664931 c.1030A>C p.K344Q Substitution - Missense 23:41141321-41141321 + p2_VII-2 COSM1738290 c.7054A>C p.T2352P Substitution - Missense 23:41225130-41225130 + TCGA-AP-A051-01 COSM1599387 c.5869G>A p.D1957N Substitution - Missense 23:41216436-41216436 + PTC_449 COSM5960097 c.6796C>T p.Q2266* Substitution - Nonsense 23:41224807-41224807 + TCGA-BR-A4QL-01 COSM1490954 c.2248C>T p.R750* Substitution - Nonsense 23:41166134-41166134 + TCGA-AP-A056-01 COSM1599416 c.680A>C p.K227T Substitution - Missense 23:41140681-41140681 + T2944 COSM4739955 c.75_76insC p.L28fs*10 Insertion - Frameshift 23:41123703-41123704 + MDA-N COSM1682561 c.944C>T p.P315L Substitution - Missense 23:41141160-41141160 + TCGA-BG-A0W1-01 COSM1155367 c.628C>G p.R210G Substitution - Missense 23:41136996-41136996 + HCC086T COSM5813067 c.1963C>T p.Q655* Substitution - Nonsense 23:41162855-41162855 + DM10 COSM5611143 c.623G>T p.R208L Substitution - Missense 23:41137012-41137012 + 11114 COSM5751558 c.5251_5253delCTT p.L1751delL Deletion - In frame 23:41214629-41214631 + MO_1241 COSM5556366 c.5935C>A p.H1979N Substitution - Missense 23:41216502-41216502 + pfg181T COSM270533 c.7410+3delA p.? Unknown 23:41229782-41229782 + OSCC-GB_00250111 COSM1490960 c.4300C>T p.Q1434* Substitution - Nonsense 23:41197451-41197451 + 8047575 COSM3390634 c.1428A>G p.Q476Q Substitution - coding silent 23:41148398-41148398 + TCGA-AX-A063-01 COSM1121322 c.546T>A p.G182G Substitution - coding silent 23:41136935-41136935 + TCGA-D9-A6EC-06 COSM4401507 c.3887T>C p.F1296S Substitution - Missense 23:41189385-41189385 + AOCS-088-3-8 COSM4149048 c.5670G>A p.W1890* Substitution - Nonsense 23:41216258-41216258 + TCGA-AA-3966-01 COSM273451 c.5598T>G p.G1866G Substitution - coding silent 23:41216186-41216186 + p2_VI-2 COSM1738290 c.7054A>C p.T2352P Substitution - Missense 23:41225130-41225130 + TCGA-AP-A0LM-01 COSM1599378 c.7422T>C p.C2474C Substitution - coding silent 23:41229770-41229770 + TCGA-CZ-4861-01 COSM165461 c.2175A>G p.L725L Substitution - coding silent 23:41166082-41166082 + CSCC-15-T COSM1121345 c.3737C>T p.S1246L Substitution - Missense 23:41188065-41188065 + TCGA-B5-A0JY-01 COSM1599408 c.2004T>C p.G668G Substitution - coding silent 23:41165890-41165890 + TCGA-CM-5864-01 COSM1467967 c.4199T>G p.L1400R Substitution - Missense 23:41196725-41196725 + p2_IV-1 COSM1738291 c.7033A>C p.T2345P Substitution - Missense 23:41225130-41225130 + PT49 COSM5936827 c.6773C>T p.S2258L Substitution - Missense 23:41224784-41224784 + TCGA-D1-A103-01 COSM1599407 c.2545C>T p.R849* Substitution - Nonsense 23:41168127-41168127 + TCGA-A2-A1FV-01 COSM1490950 c.273_274delAG p.E93fs*10 Deletion - Frameshift 23:41131487-41131488 + S01567 COSM4386728 c.198_199insT p.P68fs*4 Insertion - Frameshift 23:41129101-41129102 + TCGA-D8-A1XZ-01 COSM1490952 c.1782C>T p.D594D Substitution - coding silent 23:41152987-41152987 + TCGA-BR-4368-01 COSM4109469 c.1876+2T>C p.? Unknown 23:41153083-41153083 + TCGA-BR-8078-01 COSM4109493 c.5954G>A p.R1985Q Substitution - Missense 23:41216542-41216542 + PD4134a COSM165458 c.5260G>T p.D1754Y Substitution - Missense 23:41214659-41214659 + TCGA-AP-A0LM-01 COSM1599380 c.6897C>T p.T2299T Substitution - coding silent 23:41224887-41224887 + T3446 COSM1599397 c.4096_4097delAG p.R1368fs*2 Deletion - Frameshift 23:41196601-41196602 + CSCC-7-T COSM4571973 c.6029T>C p.L2010P Substitution - Missense 23:41216617-41216617 + TCGA-G4-6628-01 COSM1467949 c.194C>A p.P65H Substitution - Missense 23:41129097-41129097 + PT09_1 COSM5895122 c.2637-1G>A p.? Unknown 23:41169994-41169994 + TCGA-D1-A103-01 COSM1121337 c.2790C>T p.G930G Substitution - coding silent 23:41170169-41170169 + pfg016T COSM1644032 c.7434delA p.A2481fs*7 Deletion - Frameshift 23:41229782-41229782 + CSCC-7-T COSM4571972 c.6050T>C p.L2017P Substitution - Missense 23:41216617-41216617 + XHDG04 COSM4768394 c.6422G>T p.G2141V Substitution - Missense 23:41218584-41218584 + TCGA-AX-A0J1-01 COSM1599402 c.3144G>A p.P1048P Substitution - coding silent 23:41171954-41171954 + PT51 COSM5938548 c.234G>A p.M78I Substitution - Missense 23:41129137-41129137 + TCGA-EB-A5UL-06 COSM3561677 c.3472T>C p.L1158L Substitution - coding silent 23:41184589-41184589 + TCGA-02-0047-01 COSM2149003 c.5620C>T p.Q1874* Substitution - Nonsense 23:41216187-41216187 + CSB1 COSM5028900 c.6091G>T p.E2031* Substitution - Nonsense 23:41217246-41217246 + MO_1241 COSM5556367 c.5914C>A p.H1972N Substitution - Missense 23:41216502-41216502 + TCGA-B5-A11J-01 COSM1121317 c.285A>G p.E95E Substitution - coding silent 23:41131499-41131499 + TCGA-C5-A3HE-01 COSM1467963 c.2729G>A p.R910Q Substitution - Missense 23:41170108-41170108 + XHDG04 COSM4768395 c.6401G>T p.G2134V Substitution - Missense 23:41218584-41218584 + TL67 COSM5752012 c.6593_6594insAGCGCC p.F2198>LAP Complex - insertion inframe 23:41223265-41223266 + TCGA-BP-5168-01 COSM1138148 c.7151C>A p.A2384E Substitution - Missense 23:41229342-41229342 + ESCC_BICR_011T COSM5436128 c.4127T>G p.F1376C Substitution - Missense 23:41196632-41196632 + TCGA-02-0047 COSM2149004 c.5599C>T p.Q1867* Substitution - Nonsense 23:41216187-41216187 + HN_62686 COSM130133 c.3293C>T p.P1098L Substitution - Missense 23:41184431-41184431 + SNU-175 COSM1121331 c.1775G>A p.R592H Substitution - Missense 23:41152980-41152980 + B52 COSM1756566 c.2222A>C p.N741T Substitution - Missense 23:41166129-41166129 + TCGA-EL-A3H5-01 COSM3372266 c.5393A>C p.K1798T Substitution - Missense 23:41215960-41215960 + TCGA-G4-6588-01 COSM1467977 c.5587G>A p.V1863I Substitution - Missense 23:41216175-41216175 + TCGA-F5-6814-01 COSM3424794 c.5594T>G p.L1865R Substitution - Missense 23:41216161-41216161 + TCGA-F5-6814-01 COSM3424795 c.5573T>G p.L1858R Substitution - Missense 23:41216161-41216161 + TCGA-DU-6410-01 COSM3973660 c.4367T>C p.I1456T Substitution - Missense 23:41198535-41198535 + PD6412a COSM5752393 c.3280-2_3281delAGGT p.? Unknown 23:41184395-41184398 + 1N64-VS-1T64 COSM4978099 c.939_945delTTTGAAG p.L314fs*2 Deletion - Frameshift 23:41141134-41141140 + OSCC-GB_00800111 COSM4887844 c.2063C>A p.A688E Substitution - Missense 23:41165949-41165949 + YUJUBE COSM5412678 c.2024C>T p.P675L Substitution - Missense 23:41165910-41165910 + TCGA-E9-A1RF-01 COSM1490958 c.3458C>G p.T1153S Substitution - Missense 23:41184596-41184596 + Pat_41_B COSM5877850 c.2432C>T p.S811F Substitution - Missense 23:41168035-41168035 + OSCC-GB_00220111 COSM3713901 c.1763+1G>T p.? Unknown 23:41151058-41151058 + TCGA-B5-A0JR-01 COSM1121344 c.3518_3519delGT p.V1174fs*12 Deletion - Frameshift 23:41184656-41184657 + pfg181T COSM4753514 c.1046A>G p.N349S Substitution - Missense 23:41141316-41141316 + TCGA-AX-A0J1-01 COSM1121330 c.1636G>T p.D546Y Substitution - Missense 23:41150951-41150951 + TCGA-BS-A0UV-01 COSM1121351 c.4647C>T p.F1549F Substitution - coding silent 23:41201124-41201124 + MI4 COSM612953 c.2228G>A p.R743Q Substitution - Missense 23:41166135-41166135 + TCGA-BS-A0UF-01 COSM1121325 c.864A>C p.K288N Substitution - Missense 23:41141080-41141080 + TCGA-AP-A0LM-01 COSM1121370 c.6876C>T p.T2292T Substitution - coding silent 23:41224887-41224887 + TCGA-A8-A0A6-01 COSM3844700 c.5472T>G p.G1824G Substitution - coding silent 23:41216060-41216060 + CPCG_0099_Pr_P_F0 COSM3396426 c.5245C>T p.Q1749* Substitution - Nonsense 23:41214644-41214644 + RK131_C01 COSM3701853 c.1964+10A>G p.? Unknown 23:41162887-41162887 + TCGA-CJ-4881-01 COSM95502 c.6338T>C p.I2113T Substitution - Missense 23:41218521-41218521 + p2_I-2 COSM1738290 c.7054A>C p.T2352P Substitution - Missense 23:41225130-41225130 + TCGA-BG-A0MQ-01 COSM1121347 c.4075_4076delAG p.R1361fs*2 Deletion - Frameshift 23:41196601-41196602 + DLD1 COSM4626568 c.5605A>G p.S1869G Substitution - Missense 23:41216193-41216193 + TCGA-AX-A063-01 COSM1599417 c.567T>A p.G189G Substitution - coding silent 23:41136935-41136935 + TCGA-BR-8366-01 COSM4109472 c.2509A>G p.K837E Substitution - Missense 23:41168091-41168091 + tumor_4134005 COSM3357440 c.311T>C p.L104P Substitution - Missense 23:41131525-41131525 + TCGA-BF-A3DL-01 COSM4904966 c.6031C>T p.Q2011* Substitution - Nonsense 23:41216598-41216598 + TCGA-G4-6588-01 COSM1467976 c.5608G>A p.V1870I Substitution - Missense 23:41216175-41216175 + TCGA-A5-A0VP-01 COSM1599391 c.5303C>T p.A1768V Substitution - Missense 23:41214681-41214681 + TCGA-D1-A165-01 COSM1155375 c.5359A>T p.K1787* Substitution - Nonsense 23:41215926-41215926 + p2_IV-1 COSM1738290 c.7054A>C p.T2352P Substitution - Missense 23:41225130-41225130 + TCGA-D3-A51G-06 COSM3561681 c.3616C>T p.P1206S Substitution - Missense 23:41186574-41186574 + TCGA-EW-A1J5-01 COSM1490960 c.4300C>T p.Q1434* Substitution - Nonsense 23:41197451-41197451 + TCGA-FE-A22Z-01 COSM3372261 c.181G>T p.E61* Substitution - Nonsense 23:41129084-41129084 + TCGA-02-0047 COSM2149003 c.5620C>T p.Q1874* Substitution - Nonsense 23:41216187-41216187 + T3720 COSM4739960 c.2492_2493delAC p.D831fs*3 Deletion - Frameshift 23:41168095-41168096 + OSCC-GB_00240111 COSM3713950 c.5041G>A p.E1681K Substitution - Missense 23:41210555-41210555 + TCGA-CJ-5672-01 COSM488366 c.1710T>C p.C570C Substitution - coding silent 23:41151025-41151025 + CG14 COSM5422879 c.6010C>G p.Q2004E Substitution - Missense 23:41216598-41216598 + RK071_C01 COSM1636546 c.6565C>T p.L2189F Substitution - Missense 23:41223237-41223237 + J57_T COSM3965251 c.3027+8G>C p.? Unknown 23:41170627-41170627 + TCGA-DI-A0WH-01 COSM1155370 c.2731A>G p.T911A Substitution - Missense 23:41170089-41170089 + LPJ023 COSM1315995 c.1515G>A p.W505* Substitution - Nonsense 23:41148485-41148485 + WSU-HN30 COSM4600653 c.6428C>G p.S2143C Substitution - Missense 23:41218590-41218590 + SC_9081 COSM5547222 c.316delA p.K107fs*18 Deletion - Frameshift 23:41131530-41131530 + TCGA-34-5929-01 COSM1151636 c.4272G>C p.E1424D Substitution - Missense 23:41197402-41197402 + 06-P036 COSM4589421 c.270G>A p.P90P Substitution - coding silent 23:41131484-41131484 + TCGA-AA-3492-01 COSM1467965 c.4052T>C p.F1351S Substitution - Missense 23:41196346-41196346 + ESCC_107 COSM5650076 c.3007-5_3007-2delTCTA p.? Unknown 23:41171833-41171836 + B59-Tumor COSM1756569 c.6419C>T p.P2140L Substitution - Missense 23:41218581-41218581 + TCGA-D8-A1X7-01 COSM1490955 c.2227C>T p.R743* Substitution - Nonsense 23:41166134-41166134 + LOVO COSM1599380 c.6897C>T p.T2299T Substitution - coding silent 23:41224887-41224887 + B80-Tumor COSM1756567 c.2973T>C p.G991G Substitution - coding silent 23:41170565-41170565 + TCGA-FS-A1Z0-06 COSM3561685 c.4471G>A p.V1491I Substitution - Missense 23:41198618-41198618 + 11114 COSM5751559 c.5230_5232delCTT p.L1744delL Deletion - In frame 23:41214629-41214631 + CPCG_0099_Pr_P_F0 COSM3396425 c.5266C>T p.Q1756* Substitution - Nonsense 23:41214644-41214644 + TCGA-D1-A101-01 COSM1155366 c.545G>A p.C182Y Substitution - Missense 23:41136913-41136913 + TCGA-D1-A17D-01 COSM1155369 c.2394G>T p.T798T Substitution - coding silent 23:41167547-41167547 + T3446 COSM1121347 c.4075_4076delAG p.R1361fs*2 Deletion - Frameshift 23:41196601-41196602 + T3021 COSM1270120 c.7433_7434insA p.A2481fs*17 Insertion - Frameshift 23:41229781-41229782 + SC_9061 COSM5572210 c.1284G>C p.W428C Substitution - Missense 23:41143434-41143434 + TCGA-AB-2847-03 COSM1319438 c.4426C>A p.Q1476K Substitution - Missense 23:41198573-41198573 + 31119 COSM5044169 c.2021C>T p.A674V Substitution - Missense 23:41165907-41165907 + TCGA-FS-A1Z0-06 COSM3913996 c.4065+2T>G p.? Unknown 23:41196361-41196361 + sysucc-880T COSM5463861 c.543T>C p.N181N Substitution - coding silent 23:41136932-41136932 + TCGA-BR-4256-01 COSM4109476 c.2648G>C p.G883A Substitution - Missense 23:41170006-41170006 + TCGA-27-1838-01 COSM3406373 c.5738G>C p.C1913S Substitution - Missense 23:41216326-41216326 + C086 COSM5541503 c.142C>T p.P48S Substitution - Missense 23:41129045-41129045 + TCGA-66-2786-01 COSM1151640 c.5955A>T p.S1985S Substitution - coding silent 23:41216522-41216522 + 24T COSM3713950 c.5041G>A p.E1681K Substitution - Missense 23:41210555-41210555 + STC232 COSM2964733 c.76delC p.L28fs*51 Deletion - Frameshift 23:41123704-41123704 + TCGA-DK-A3X1-01 COSM3800598 c.1636G>C p.D546H Substitution - Missense 23:41150951-41150951 + 2215528 COSM612949 c.4994G>T p.R1665M Substitution - Missense 23:41205493-41205493 + TCGA-AP-A059-01 COSM1121369 c.6829A>C p.S2277R Substitution - Missense 23:41224840-41224840 + Gp5D COSM2964865 c.4866A>G p.Q1622Q Substitution - coding silent 23:41205344-41205344 + OSCC-GB_00940111 COSM4891675 c.3915G>T p.W1305C Substitution - Missense 23:41189434-41189434 + sysucc-880T COSM5463860 c.564T>C p.N188N Substitution - coding silent 23:41136932-41136932 + 25T COSM1490959 c.4321C>T p.Q1441* Substitution - Nonsense 23:41197451-41197451 + PT17_1 COSM5899229 c.6773C>T p.P2258L Substitution - Missense 23:41224763-41224763 + TCGA-66-2734-01 COSM757281 c.416G>T p.G139V Substitution - Missense 23:41134818-41134818 + 587376 COSM1232130 c.1112G>A p.R371Q Substitution - Missense 23:41141382-41141382 + TCGA-CC-A3MA-01 COSM4942922 c.7377A>G p.T2459T Substitution - coding silent 23:41229746-41229746 + 31119 COSM5044170 c.2000C>T p.A667V Substitution - Missense 23:41165907-41165907 + TCGA-BG-A0MQ-01 COSM1599397 c.4096_4097delAG p.R1368fs*2 Deletion - Frameshift 23:41196601-41196602 + TCGA-B5-A11E-01 COSM1599412 c.1419+2T>G p.? Unknown 23:41144628-41144628 + TCGA-ER-A198-06 COSM3561670 c.88C>T p.Q30* Substitution - Nonsense 23:41123716-41123716 + TCGA-D3-A51G-06 COSM3561682 c.3595C>T p.P1199S Substitution - Missense 23:41186574-41186574 + TCGA-DM-A28M-01 COSM3694582 c.270G>T p.P90P Substitution - coding silent 23:41131484-41131484 + TCGA-AA-3663-01 COSM1467956 c.1675C>A p.L559I Substitution - Missense 23:41150969-41150969 + TCGA-CC-A3M9-01 COSM4928411 c.1782C>T p.P594P Substitution - coding silent 23:41152966-41152966 + TCGA-AP-A0LM-01 COSM1121372 c.7401T>C p.C2467C Substitution - coding silent 23:41229770-41229770 + TCGA-C5-A1BM-01 COSM4826418 c.6310G>A p.E2104K Substitution - Missense 23:41218493-41218493 + TCGA-C5-A1BM-01 COSM4826417 c.6331G>A p.E2111K Substitution - Missense 23:41218493-41218493 + SM2-1 COSM3727625 c.6808C>T p.P2270S Substitution - Missense 23:41224798-41224798 + TCGA-B5-A11E-01 COSM1121356 c.5310+1G>A p.? Unknown 23:41214710-41214710 + DLD1 COSM4626567 c.5626A>G p.S1876G Substitution - Missense 23:41216193-41216193 + TCGA-A3-3387-01 COSM1138146 c.6776T>C p.F2259S Substitution - Missense 23:41224766-41224766 + TCGA-AX-A0J0-01 COSM1599398 c.4005G>A p.Q1335Q Substitution - coding silent 23:41196278-41196278 + TCGA-FW-A3R5-06 COSM3913997 c.6910C>T p.R2304C Substitution - Missense 23:41224900-41224900 + PT17_1 COSM5899230 c.6752C>T p.P2251L Substitution - Missense 23:41224763-41224763 + CSCC-31-T COSM4496383 c.4740C>T p.S1580S Substitution - coding silent 23:41201196-41201196 + TCGA-CJ-5672-01 COSM1138144 c.1731T>C p.C577C Substitution - coding silent 23:41151025-41151025 + PTC-14C COSM1151632 c.416G>T p.G139V Substitution - Missense 23:41134818-41134818 + 308_T COSM3965250 c.2707G>A p.D903N Substitution - Missense 23:41170086-41170086 + TCGA-61-1727-01 COSM1331870 c.266T>G p.L89W Substitution - Missense 23:41131480-41131480 + TL63 COSM5751987 c.352_353insT p.R118fs*5 Insertion - Frameshift 23:41134754-41134755 + ICGC_MB69 COSM3764998 c.4613C>T p.A1538V Substitution - Missense 23:41201069-41201069 + TCGA-MI-A75C-01 COSM4923111 c.1216C>G p.Q406E Substitution - Missense 23:41143345-41143345 + ICGC_MB69 COSM3764999 c.4592C>T p.A1531V Substitution - Missense 23:41201069-41201069 + CSB1 COSM5028897 c.5799G>A p.M1933I Substitution - Missense 23:41216366-41216366 + 587222 COSM1232126 c.2933G>T p.G978V Substitution - Missense 23:41170546-41170546 + ESO-580 COSM1270120 c.7433_7434insA p.A2481fs*17 Insertion - Frameshift 23:41229781-41229782 + TCGA-D3-A51G-06 COSM3561680 c.3468C>T p.G1156G Substitution - coding silent 23:41184606-41184606 + MN-105 COSM1578640 c.5160C>T p.C1720C Substitution - coding silent 23:41210674-41210674 + TCGA-AX-A0J0-01 COSM1121346 c.3984G>A p.Q1328Q Substitution - coding silent 23:41196278-41196278 + 420 COSM4432128 c.2437G>T p.E813* Substitution - Nonsense 23:41168019-41168019 + 9583_CLM COSM5757543 c.7075C>T p.R2359* Substitution - Nonsense 23:41229287-41229287 + TCGA-AP-A059-01 COSM1121332 c.1836C>T p.N612N Substitution - coding silent 23:41153041-41153041 + TCGA-AB-3001-03 COSM166875 c.1728G>A p.A576A Substitution - coding silent 23:41151043-41151043 + T23 COSM1121348 c.4098C>T p.G1366G Substitution - coding silent 23:41196624-41196624 + BRC13 COSM5028896 c.2101G>A p.E701K Substitution - Missense 23:41166008-41166008 + BD72T COSM5513784 c.4333_4334insA p.F1447fs*6 Insertion - Frameshift 23:41197463-41197464 + TCGA-EE-A2MF-06 COSM1599404 c.2876C>T p.S959L Substitution - Missense 23:41170234-41170234 + TCGA-AR-A2LE-01 COSM3844690 c.1566C>T p.L522L Substitution - coding silent 23:41148536-41148536 + Karpas-1106P COSM2964868 c.4871G>A p.S1624N Substitution - Missense 23:41205370-41205370 + TCGA-EM-A4FM-01 COSM3372262 c.4603+2T>C p.? Unknown 23:41198752-41198752 + SM2-1 COSM3727626 c.6787C>T p.P2263S Substitution - Missense 23:41224798-41224798 + TCGA-CK-5912-01 COSM1467995 c.7127_7128insT p.K2377fs*1 Insertion - Frameshift 23:41229318-41229319 + CSCC-11-T COSM4450639 c.7411-1G>A p.? Unknown 23:41230500-41230500 + T3090 COSM4739956 c.75_76insC p.L28fs*10 Insertion - Frameshift 23:41123703-41123704 + TCGA-FS-A1Z0-06 COSM3913995 c.4086+2T>G p.? Unknown 23:41196361-41196361 + TCGA-D1-A176-01 COSM1121368 c.6723A>G p.S2241S Substitution - coding silent 23:41223395-41223395 + BD173T COSM5500304 c.7227C>T p.T2409T Substitution - coding silent 23:41229596-41229596 + TCGA-FE-A22Z-01 COSM3372260 c.181G>T p.E61* Substitution - Nonsense 23:41129084-41129084 + 3N60-VS-3T60 COSM4984351 c.3815A>G p.N1272S Substitution - Missense 23:41189313-41189313 + TCGA-B0-4712-01 COSM488369 c.6952-1G>T p.? Unknown 23:41225048-41225048 + TCGA-A2-A1FV-01 COSM1490949 c.273_274delAG p.E93fs*10 Deletion - Frameshift 23:41131487-41131488 + TCGA-AP-A0LM-01 COSM1599394 c.4591A>G p.T1531A Substitution - Missense 23:41198738-41198738 + PCSI_0106_Pa_P COSM216864 c.6108C>T p.I2036I Substitution - coding silent 23:41217263-41217263 + TCGA-C5-A3HE-01 COSM1467962 c.2750G>A p.R917Q Substitution - Missense 23:41170108-41170108 + HCC65T COSM1625890 c.4380+2T>A p.? Unknown 23:41197512-41197512 + TCGA-BR-A4QL-01 COSM4109492 c.5975G>A p.R1992Q Substitution - Missense 23:41216542-41216542 + TCGA-AX-A0J1-01 COSM1599379 c.7007_7008insT p.L2337fs*11 Insertion - Frameshift 23:41225083-41225084 + TCGA-HU-8602-01 COSM4109483 c.4631G>A p.R1544H Substitution - Missense 23:41201108-41201108 + pfg181T COSM1644032 c.7434delA p.A2481fs*7 Deletion - Frameshift 23:41229782-41229782 + PD8617a COSM5752445 c.419delG p.W140fs*1 Deletion - Frameshift 23:41134821-41134821 + ESO-580 COSM272113 c.7410+2_7410+3insA p.? Unknown 23:41229781-41229782 + TCGA-66-2734-01 COSM1151632 c.416G>T p.G139V Substitution - Missense 23:41134818-41134818 + TCGA-AP-A0LM-01 COSM1121363 c.6215G>A p.R2072H Substitution - Missense 23:41218398-41218398 + TCGA-34-5929-01 COSM757275 c.4966G>C p.V1656L Substitution - Missense 23:41205465-41205465 + TCGA-D1-A16F-01 COSM1121349 c.4512C>T p.G1504G Substitution - coding silent 23:41198680-41198680 + TL42 COSM5751870 c.3734G>AG p.G1245fs*8 Complex - frameshift 23:41188062-41188062 + HCC125 COSM1625888 c.4364G>A p.G1455D Substitution - Missense 23:41197494-41197494 + B21-Tumor COSM4005082 c.1483G>A p.V495M Substitution - Missense 23:41148453-41148453 + TL63 COSM5751988 c.352_353insT p.R118fs*5 Insertion - Frameshift 23:41134754-41134755 + TCGA-D8-A1XZ-01 COSM1490951 c.1803C>T p.D601D Substitution - coding silent 23:41152987-41152987 + DM45 COSM5611146 c.2331C>T p.V777V Substitution - coding silent 23:41167484-41167484 + 401 COSM4429727 c.5725A>T p.M1909L Substitution - Missense 23:41216313-41216313 + S01023 COSM5666884 c.2269G>A p.D757N Substitution - Missense 23:41166176-41166176 + PD4203a COSM165459 c.6247C>G p.H2083D Substitution - Missense 23:41218430-41218430 + OSCC-GB_00250111 COSM1490959 c.4321C>T p.Q1441* Substitution - Nonsense 23:41197451-41197451 + PT50 COSM5937922 c.6211C>T p.L2071F Substitution - Missense 23:41218394-41218394 + TCGA-BR-A4QL-01 COSM1490955 c.2227C>T p.R743* Substitution - Nonsense 23:41166134-41166134 + TCGA-BS-A0UF-01 COSM1599388 c.5555A>C p.Q1852P Substitution - Missense 23:41216122-41216122 + H1155 COSM1195398 c.5615G>A p.S1872N Substitution - Missense 23:41216182-41216182 + OSCC-GB_01090111 COSM4886505 c.423G>T p.K141N Substitution - Missense 23:41134825-41134825 + 22T COSM3713902 c.1742+1G>T p.? Unknown 23:41151058-41151058 + TCGA-61-1900-01 COSM1331868 c.1054A>G p.M352V Substitution - Missense 23:41141324-41141324 + OSCC-GB_00020111 COSM3713947 c.536A>G p.N179S Substitution - Missense 23:41136904-41136904 + p2_VII-3 COSM1738290 c.7054A>C p.T2352P Substitution - Missense 23:41225130-41225130 + PTC-14C COSM757281 c.416G>T p.G139V Substitution - Missense 23:41134818-41134818 + ESCC_BICR_041T COSM5441469 c.1336G>A p.V446M Substitution - Missense 23:41144543-41144543 + ESCC_4 COSM5623033 c.4612C>T p.L1538L Substitution - coding silent 23:41201089-41201089 + 587376 COSM1232133 c.3445A>G p.K1149E Substitution - Missense 23:41184583-41184583 + TCGA-CJ-4881-01 COSM3364003 c.6359T>C p.I2120T Substitution - Missense 23:41218521-41218521 + TCGA-A8-A0A6-01 COSM3844704 c.5812T>G p.W1938G Substitution - Missense 23:41216400-41216400 + TCGA-EW-A1J5-01 COSM1490959 c.4321C>T p.Q1441* Substitution - Nonsense 23:41197451-41197451 + TCGA-66-2763-01 COSM1151633 c.923C>A p.S308* Substitution - Nonsense 23:41141118-41141118 + T3262 COSM4739964 c.7204G>T p.G2402* Substitution - Nonsense 23:41229573-41229573 + TCGA-FS-A1ZK-06 COSM3561690 c.5318C>T p.T1773I Substitution - Missense 23:41215906-41215906 + TCGA-BH-A18U-01 COSM3844696 c.3855G>A p.M1285I Substitution - Missense 23:41189374-41189374 + TCGA-AP-A056-01 COSM1599410 c.1796G>A p.R599H Substitution - Missense 23:41152980-41152980 + ESCC_140 COSM5643471 c.3400A>G p.M1134V Substitution - Missense 23:41184538-41184538 + TCGA-A2-A0T3-01 COSM1490961 c.5365T>C p.L1789L Substitution - coding silent 23:41215932-41215932 + CHC1603T COSM4801830 c.4171A>G p.I1391V Substitution - Missense 23:41196676-41196676 + T2944 COSM4739956 c.75_76insC p.L28fs*10 Insertion - Frameshift 23:41123703-41123704 + TCGA-B5-A11N-01 COSM1599406 c.2644C>T p.R882C Substitution - Missense 23:41170002-41170002 + H1703 COSM1196599 c.697G>T p.G233W Substitution - Missense 23:41140698-41140698 + 25T COSM1490960 c.4300C>T p.Q1434* Substitution - Nonsense 23:41197451-41197451 + 46T COSM3713952 c.7237G>T p.E2413* Substitution - Nonsense 23:41229606-41229606 + Pat_41_B COSM5877847 c.1219C>T p.P407S Substitution - Missense 23:41143348-41143348 + TCGA-D7-6527-01 COSM4109491 c.5801G>A p.R1934H Substitution - Missense 23:41216389-41216389 + TCGA-AP-A059-01 COSM1599409 c.1857C>T p.N619N Substitution - coding silent 23:41153041-41153041 + TCGA-27-1838-01 COSM3406372 c.5759G>C p.C1920S Substitution - Missense 23:41216326-41216326 + CPCG0099-F1 COSM3396426 c.5245C>T p.Q1749* Substitution - Nonsense 23:41214644-41214644 + TCGA-AP-A0LM-01 COSM1599384 c.6236G>A p.R2079H Substitution - Missense 23:41218398-41218398 + WT028 COSM1121348 c.4098C>T p.G1366G Substitution - coding silent 23:41196624-41196624 + TCGA-P4-A5EA-01 COSM3992476 c.1983T>C p.L661L Substitution - coding silent 23:41162875-41162875 + PD11372a COSM5767308 c.7111G>C p.D2371H Substitution - Missense 23:41229302-41229302 + TCGA-A7-A26J-01 COSM1490962 c.6586C>G p.L2196V Substitution - Missense 23:41223237-41223237 + TCGA-AZ-4682-01 COSM1467990 c.6543A>T p.L2181F Substitution - Missense 23:41219230-41219230 + TCGA-AP-A056-01 COSM1121324 c.659A>C p.K220T Substitution - Missense 23:41140681-41140681 + TBR08 COSM4168297 c.3408_3409insCAAC p.R1137fs*11 Insertion - Frameshift 23:41184546-41184547 + TCGA-B5-A11E-01 COSM1121367 c.6437G>A p.S2146N Substitution - Missense 23:41219124-41219124 + CSCC-17-T COSM4530856 c.1712G>C p.S571T Substitution - Missense 23:41151027-41151027 + ESCC_BICR_011T COSM5436129 c.4106T>G p.F1369C Substitution - Missense 23:41196632-41196632 + MDA-MB-435 COSM1682560 c.965C>T p.P322L Substitution - Missense 23:41141160-41141160 + 6115115 COSM5547829 c.7048_7049delTG p.W2350fs*7 Deletion - Frameshift 23:41225124-41225125 + TCGA-B5-A11E-01 COSM1121316 c.177G>A p.Q59Q Substitution - coding silent 23:41129080-41129080 + TCGA-BT-A0YX-01 COSM1133866 c.6248A>T p.N2083I Substitution - Missense 23:41218410-41218410 + TCGA-AO-A12H-01 COSM457506 c.6933_6934insA p.S2312fs*2 Insertion - Frameshift 23:41224944-41224945 + DM10 COSM5611141 c.321G>T p.K107N Substitution - Missense 23:41131535-41131535 + TCGA-AP-A0LM-01 COSM1121362 c.6132C>A p.F2044L Substitution - Missense 23:41217287-41217287 + TCGA-B6-A0X7-01 COSM1490953 c.2225G>A p.R742Q Substitution - Missense 23:41166111-41166111 + B59-Tumor COSM1756570 c.6398C>T p.P2133L Substitution - Missense 23:41218581-41218581 + TCGA-61-1995-01 COSM73237 c.5714A>G p.D1905G Substitution - Missense 23:41216302-41216302 + OSCC-GB_00010111 COSM1636541 c.6284A>G p.N2095S Substitution - Missense 23:41218446-41218446 + DM10 COSM5611140 c.321G>T p.K107N Substitution - Missense 23:41131535-41131535 + TCGA-HU-A4H3-01 COSM4109487 c.5020C>T p.R1674C Substitution - Missense 23:41210534-41210534 + TCGA-AX-A1C8-01 COSM1155374 c.5263G>A p.E1755K Substitution - Missense 23:41214641-41214641 + TCGA-AX-A060-01 COSM1121347 c.4075_4076delAG p.R1361fs*2 Deletion - Frameshift 23:41196601-41196602 + 587376 COSM1232132 c.3466A>G p.K1156E Substitution - Missense 23:41184583-41184583 + TCGA-AO-A12H-01 COSM1490964 c.6954_6955insA p.S2319fs*2 Insertion - Frameshift 23:41224944-41224945 + PD8984a COSM5769362 c.4492A>T p.I1498F Substitution - Missense 23:41198639-41198639 + TCGA-CA-6718-01 COSM1467970 c.4973G>A p.R1658Q Substitution - Missense 23:41205451-41205451 + p2_II-2 COSM1738291 c.7033A>C p.T2345P Substitution - Missense 23:41225130-41225130 + SW620 COSM2964896 c.5751G>C p.E1917D Substitution - Missense 23:41216339-41216339 + CPCG0099-F1 COSM3396425 c.5266C>T p.Q1756* Substitution - Nonsense 23:41214644-41214644 + TCGA-MI-A75C-01 COSM4923112 c.1195C>G p.Q399E Substitution - Missense 23:41143345-41143345 + TCGA-D5-6538-01 COSM1467981 c.5852delT p.Y1953fs*7 Deletion - Frameshift 23:41216419-41216419 + WSU-HN30 COSM4600654 c.6407C>G p.S2136C Substitution - Missense 23:41218590-41218590 + TCGA-DA-A1HV-06 COSM3561688 c.5054C>T p.S1685L Substitution - Missense 23:41210568-41210568 + TCGA-AA-3715-01 COSM270533 c.7410+3delA p.? Unknown 23:41229782-41229782 + p2_VII-3 COSM1738291 c.7033A>C p.T2345P Substitution - Missense 23:41225130-41225130 + TCGA-GM-A2DB-01 COSM3844702 c.5779A>C p.M1927L Substitution - Missense 23:41216367-41216367 + TBR08 COSM4168298 c.3431G>C p.R1144P Substitution - Missense 23:41184548-41184548 + TCGA-EE-A3AF-06 COSM3561674 c.1568G>A p.S523N Substitution - Missense 23:41148538-41148538 + 587222 COSM1232125 c.2954G>T p.G985V Substitution - Missense 23:41170546-41170546 + OSCC-GB_00020111 COSM3713948 c.515A>G p.N172S Substitution - Missense 23:41136904-41136904 + RK208_C01 COSM1636540 c.6256_6257insT p.N2088fs*1 Insertion - Frameshift 23:41218439-41218440 + PD8984a COSM5769363 c.4471A>T p.I1491F Substitution - Missense 23:41198639-41198639 + DM55 COSM5611148 c.5216C>T p.T1739I Substitution - Missense 23:41214594-41214594 + TCGA-UB-A7ME-01 COSM4910206 c.4998T>A p.L1666L Substitution - coding silent 23:41210512-41210512 + TCGA-CM-6162-01 COSM1467985 c.6191G>A p.R2064H Substitution - Missense 23:41217325-41217325 + TCGA-BR-4361-01 COSM4109485 c.4920T>C p.L1640L Substitution - coding silent 23:41205419-41205419 + J57_T COSM3965252 c.3006+8G>C p.? Unknown 23:41170627-41170627 + SJTALL007 COSM306011 c.2403+1G>C p.? Unknown 23:41167578-41167578 + TCGA-CM-6162-01 COSM1467986 c.6170G>A p.R2057H Substitution - Missense 23:41217325-41217325 + H1155 COSM1195859 c.691C>T p.H231Y Substitution - Missense 23:41140713-41140713 + Pat_46_B COSM5877851 c.6779G>A p.G2260D Substitution - Missense 23:41224769-41224769 + TCGA-AG-4007-01 COSM4739956 c.75_76insC p.L28fs*10 Insertion - Frameshift 23:41123703-41123704 + TCGA-A6-5665-01 COSM1467960 c.2253A>C p.E751D Substitution - Missense 23:41166139-41166139 + TCGA-43-5668-01 COSM1151634 c.1705G>C p.A569P Substitution - Missense 23:41150999-41150999 + TCGA-A8-A0A6-01 COSM3844699 c.5493T>G p.G1831G Substitution - coding silent 23:41216060-41216060 + TCGA-HU-A4GT-01 COSM4109494 c.6346T>C p.F2116L Substitution - Missense 23:41218508-41218508 + ESCC_4 COSM5623032 c.4633C>T p.L1545L Substitution - coding silent 23:41201089-41201089 + TCGA-AP-A0LL-01 COSM1155377 c.6339G>T p.R2113S Substitution - Missense 23:41218501-41218501 + TCGA-FW-A3R5-06 COSM3913998 c.6889C>T p.R2297C Substitution - Missense 23:41224900-41224900 + TCGA-FW-A3R5-06 COSM3561683 c.3985C>T p.R1329C Substitution - Missense 23:41196258-41196258 + CHC1603T COSM4801830 c.4171A>G p.I1391V Substitution - Missense 23:41196676-41196676 + TCGA-AA-3510-01 COSM1467978 c.5686C>T p.R1896C Substitution - Missense 23:41216253-41216253 + CHC1626T COSM4791650 c.1181A>G p.N394S Substitution - Missense 23:41143310-41143310 + TCGA-BT-A3PK-01 COSM3800600 c.5891A>G p.E1964G Substitution - Missense 23:41216479-41216479 + TCGA-AP-A051-01 COSM1121348 c.4098C>T p.G1366G Substitution - coding silent 23:41196624-41196624 + 2T COSM3713948 c.515A>G p.N172S Substitution - Missense 23:41136904-41136904 + TCGA-AC-A23H-01 COSM3844697 c.3894G>C p.L1298F Substitution - Missense 23:41189392-41189392 + PT09_2 COSM5895122 c.2637-1G>A p.? Unknown 23:41169994-41169994 + OSCC-GB_01070111 COSM4889377 c.1240G>T p.E414* Substitution - Nonsense 23:41143369-41143369 + TCGA-B5-A0JY-01 COSM1121333 c.1983T>C p.G661G Substitution - coding silent 23:41165890-41165890 + TCGA-A2-A0T3-01 COSM457504 c.5344T>C p.L1782L Substitution - coding silent 23:41215932-41215932 + TCGA-AP-A051-01 COSM1121327 c.1272T>C p.L424L Substitution - coding silent 23:41143422-41143422 + TCGA-AP-A056-01 COSM1121331 c.1775G>A p.R592H Substitution - Missense 23:41152980-41152980 + pfg068T COSM4753509 c.13A>G p.T5A Substitution - Missense 23:41123641-41123641 + 9583_PT COSM5757543 c.7075C>T p.R2359* Substitution - Nonsense 23:41229287-41229287 + CSB1 COSM5028899 c.6112G>T p.E2038* Substitution - Nonsense 23:41217246-41217246 + TCGA-06-5412-01 COSM3406370 c.5604G>A p.V1868V Substitution - coding silent 23:41216171-41216171 + TCGA-BP-5168-01 COSM488370 c.7130C>A p.A2377E Substitution - Missense 23:41229342-41229342 + TCGA-06-5412-01 COSM3406371 c.5583G>A p.V1861V Substitution - coding silent 23:41216171-41216171 + TCGA-D1-A103-01 COSM1599405 c.2811C>T p.G937G Substitution - coding silent 23:41170169-41170169 + REC-1 COSM1740817 c.7130C>T p.A2377V Substitution - Missense 23:41229342-41229342 + TCGA-EE-A2MR-06 COSM3561675 c.2671C>T p.R891* Substitution - Nonsense 23:41170029-41170029 + TCGA-FU-A3HZ-01 COSM4840610 c.3987C>A p.F1329L Substitution - Missense 23:41196281-41196281 + TCGA-BR-4361-01 COSM4109466 c.1094T>C p.V365A Substitution - Missense 23:41141364-41141364 + RK022_C01 COSM1636536 c.1864C>A p.L622I Substitution - Missense 23:41153069-41153069 + TCGA-BS-A0UF-01 COSM1121326 c.1231C>T p.R411C Substitution - Missense 23:41143381-41143381 + SJTALL007 COSM306011 c.2403+1G>C p.? Unknown 23:41167578-41167578 + TCGA-D1-A165-01 COSM1121339 c.3033C>T p.I1011I Substitution - coding silent 23:41171864-41171864 + DM79 COSM5611152 c.7212C>T p.I2404I Substitution - coding silent 23:41229403-41229403 + TCGA-B5-A11E-01 COSM1599382 c.6458G>A p.S2153N Substitution - Missense 23:41219124-41219124 + TCGA-AN-A0XN-01 COSM457503 c.3860_3861insA p.C1288fs*13 Insertion - Frameshift 23:41189379-41189380 + p2_VII-1 COSM1738291 c.7033A>C p.T2345P Substitution - Missense 23:41225130-41225130 + PD11372a COSM5767309 c.7090G>C p.D2364H Substitution - Missense 23:41229302-41229302 + TCGA-F5-6814-01 COSM3424792 c.4275G>T p.T1425T Substitution - coding silent 23:41197405-41197405 + RK208_C01 COSM1636541 c.6284A>G p.N2095S Substitution - Missense 23:41218446-41218446 + Pat_46_B COSM5877852 c.6758G>A p.G2253D Substitution - Missense 23:41224769-41224769 + TCGA-D1-A17D-01 COSM1121334 c.2373G>T p.T791T Substitution - coding silent 23:41167547-41167547 + AOCS-088-3-8 COSM4149047 c.5691G>A p.W1897* Substitution - Nonsense 23:41216258-41216258 + TCGA-EM-A1CV-01 COSM3372264 c.5319A>G p.K1773K Substitution - coding silent 23:41214697-41214697 + EWS502 COSM4589423 c.5436C>T p.F1812F Substitution - coding silent 23:41216003-41216003 + ccRCC-23 COSM1664930 c.1051A>C p.K351Q Substitution - Missense 23:41141321-41141321 + TCGA-BR-4256-01 COSM4109477 c.2627G>C p.G876A Substitution - Missense 23:41170006-41170006 + TCGA-D3-A3C7-06 COSM3561693 c.7303C>T p.P2435S Substitution - Missense 23:41229651-41229651 + TCGA-BR-4292-01 COSM4109460 c.594A>G p.S198S Substitution - coding silent 23:41136962-41136962 + DM59 COSM5611151 c.3985T>C p.F1329L Substitution - Missense 23:41196279-41196279 + B52 COSM1756565 c.2243A>C p.N748T Substitution - Missense 23:41166129-41166129 + 087T COSM1731218 c.2140G>T p.E714* Substitution - Nonsense 23:41166047-41166047 + TARGET-20-PAMYAS-04A-01D COSM5487466 c.6337_6338insGGCCT p.I2113fs*3 Insertion - Frameshift 23:41218520-41218521 + PT51 COSM5938547 c.234G>A p.M78I Substitution - Missense 23:41129137-41129137 + TL68 COSM5752024 c.987_988insGGGT p.N330fs*2 Insertion - Frameshift 23:41141182-41141183 + PD8617a COSM5752444 c.419delG p.W140fs*1 Deletion - Frameshift 23:41134821-41134821 + TCGA-AP-A059-01 COSM1599383 c.6424C>T p.P2142S Substitution - Missense 23:41218586-41218586 + HCC066T COSM5820972 c.5326A>T p.K1776* Substitution - Nonsense 23:41214704-41214704 + TCGA-EA-A439-01 COSM4843712 c.5704G>A p.D1902N Substitution - Missense 23:41216271-41216271 + sysucc-783T COSM5485160 c.4594G>A p.A1532T Substitution - Missense 23:41198741-41198741 + pfg181T COSM2964733 c.76delC p.L28fs*51 Deletion - Frameshift 23:41123704-41123704 + TCGA-A5-A0VP-01 COSM1121355 c.5282C>T p.A1761V Substitution - Missense 23:41214681-41214681 + TCGA-P4-A5EA-01 COSM3992477 c.1962T>C p.L654L Substitution - coding silent 23:41162875-41162875 + PD13802a COSM5025055 c.328G>C p.D110H Substitution - Missense 23:41134730-41134730 + H1703 COSM1196600 c.676G>T p.G226W Substitution - Missense 23:41140698-41140698 + OSCC-GB_00800111 COSM4887845 c.2042C>A p.A681E Substitution - Missense 23:41165949-41165949 + HCT8 COSM4635807 c.715G>A p.D239N Substitution - Missense 23:41140716-41140716 + CSCC-30-T COSM4510066 c.826C>G p.L276V Substitution - Missense 23:41141021-41141021 + LPJ023 COSM1315994 c.1536G>A p.W512* Substitution - Nonsense 23:41148485-41148485 + 0078_CRUK_PC_0078_T1_DNA COSM4420808 c.3899G>A p.S1300N Substitution - Missense 23:41189418-41189418 + HCC2998 COSM4631914 c.1888T>G p.Y630D Substitution - Missense 23:41162801-41162801 + SJDOSTEOS013 COSM5760271 c.856G>A p.E286K Substitution - Missense 23:41141072-41141072 + TCGA-DI-A0WH-01 COSM1121336 c.2710A>G p.T904A Substitution - Missense 23:41170089-41170089 + CSCC-44-T COSM4534711 c.2112G>C p.L704F Substitution - Missense 23:41165998-41165998 + TCGA-G4-6588-01 COSM1467994 c.6833A>G p.Y2278C Substitution - Missense 23:41224844-41224844 + TCGA-B5-A11N-01 COSM1599389 c.5496C>T p.V1832V Substitution - coding silent 23:41216063-41216063 + pfg181T COSM4765190 c.7410+3_7410+4insA p.? Unknown 23:41229782-41229783 + TCGA-HU-8602-01 COSM4109482 c.4652G>A p.R1551H Substitution - Missense 23:41201108-41201108 + HCC2998 COSM2964874 c.5129C>T p.S1710F Substitution - Missense 23:41210643-41210643 + TCGA-CA-6718-01 COSM1467972 c.5063A>C p.E1688A Substitution - Missense 23:41210556-41210556 + TCGA-HU-A4G6-01 COSM4109462 c.750A>G p.Q250Q Substitution - coding silent 23:41140751-41140751 + TCGA-BR-8678-01 COSM4109488 c.5080G>A p.V1694M Substitution - Missense 23:41210573-41210573 + TCGA-AZ-4682-01 COSM1467989 c.6564A>T p.L2188F Substitution - Missense 23:41219230-41219230 + TCGA-AX-A0J1-01 COSM1121348 c.4098C>T p.G1366G Substitution - coding silent 23:41196624-41196624 + TCGA-D7-8579-01 COSM1599414 c.1252C>T p.R418C Substitution - Missense 23:41143381-41143381 + TCGA-GM-A2DB-01 COSM3844701 c.5800A>C p.M1934L Substitution - Missense 23:41216367-41216367 + TCGA-FS-A1Z0-06 COSM3561686 c.4450G>A p.V1484I Substitution - Missense 23:41198618-41198618 + T3724 COSM1599397 c.4096_4097delAG p.R1368fs*2 Deletion - Frameshift 23:41196601-41196602 + HCC066T COSM5820973 c.5305A>T p.K1769* Substitution - Nonsense 23:41214704-41214704 + TCGA-B5-A0JY-01 COSM1599401 c.3159G>A p.T1053T Substitution - coding silent 23:41184008-41184008 + CSCC-44-T COSM4534712 c.2091G>C p.L697F Substitution - Missense 23:41165998-41165998 + TCGA-BR-6566-01 COSM4109470 c.1994T>C p.L665S Substitution - Missense 23:41165880-41165880 + BD72T COSM5513785 c.4312_4313insA p.F1440fs*6 Insertion - Frameshift 23:41197463-41197464 + 587284 COSM1232127 c.2164A>G p.S722G Substitution - Missense 23:41166050-41166050 + T2944 COSM4739962 c.4239G>A p.T1413T Substitution - coding silent 23:41197390-41197390 + TCGA-13-2071-01 COSM1331872 c.186T>A p.D62E Substitution - Missense 23:41129089-41129089 + p2_V-1 COSM1738291 c.7033A>C p.T2345P Substitution - Missense 23:41225130-41225130 + DM10 COSM5611138 c.5496C>A p.V1832V Substitution - coding silent 23:41216063-41216063 + TBR08 COSM4168299 c.3410G>C p.R1137P Substitution - Missense 23:41184548-41184548 + TCGA-B9-A69E-01 COSM3992478 c.3440C>T p.A1147V Substitution - Missense 23:41184557-41184557 + p2_V-1 COSM1738290 c.7054A>C p.T2352P Substitution - Missense 23:41225130-41225130 + TCGA-BH-A18G-01 COSM1121347 c.4075_4076delAG p.R1361fs*2 Deletion - Frameshift 23:41196601-41196602 + SNU-C4 COSM1121347 c.4075_4076delAG p.R1361fs*2 Deletion - Frameshift 23:41196601-41196602 + TCGA-AX-A0J1-01 COSM1121341 c.3123G>A p.P1041P Substitution - coding silent 23:41171954-41171954 + TCGA-B6-A0X7-01 COSM457501 c.2204G>A p.R735Q Substitution - Missense 23:41166111-41166111 + TCGA-66-2787-01 COSM757278 c.2372C>T p.T791M Substitution - Missense 23:41167546-41167546 + 06-P036 COSM4589422 c.270G>A p.P90P Substitution - coding silent 23:41131484-41131484 + TCGA-AA-3510-01 COSM1467979 c.5665C>T p.R1889C Substitution - Missense 23:41216253-41216253 + WA50 COSM242208 c.2986G>T p.E996* Substitution - Nonsense 23:41170599-41170599 + TCGA-EE-A2MR-06 COSM3561684 c.3964C>T p.R1322C Substitution - Missense 23:41196258-41196258 + TCGA-D3-A2JO-06 COSM3561691 c.5664T>C p.N1888N Substitution - coding silent 23:41216231-41216231 + HCC054T COSM5809613 c.5211T>C p.F1737F Substitution - coding silent 23:41214589-41214589 + TCGA-43-5668-01 COSM757279 c.1684G>C p.A562P Substitution - Missense 23:41150999-41150999 + ML3 COSM1165518 c.2334G>A p.V778V Substitution - coding silent 23:41167487-41167487 + TCGA-AZ-6598-01 COSM1467947 c.31G>A p.G11R Substitution - Missense 23:41123659-41123659 + PT50 COSM5937924 c.6169C>T p.R2057C Substitution - Missense 23:41217324-41217324 + TCGA-B5-A0K9-01 COSM1121318 c.420G>A p.W140* Substitution - Nonsense 23:41134822-41134822 + B80 COSM1756567 c.2973T>C p.G991G Substitution - coding silent 23:41170565-41170565 + TCGA-D9-A148-06 COSM3561672 c.1090C>T p.R364* Substitution - Nonsense 23:41141381-41141381 + YUJUBE COSM5412683 c.5652T>C p.D1884D Substitution - coding silent 23:41216240-41216240 + 9583_PT COSM5757542 c.7096C>T p.R2366* Substitution - Nonsense 23:41229287-41229287 + TCGA-EB-A5UL-06 COSM3561678 c.3451T>C p.L1151L Substitution - coding silent 23:41184589-41184589 + TL41 COSM5751800 c.5900G>AG p.R1967fs*22 Complex - frameshift 23:41216467-41216467 + TCGA-CM-5862-01 COSM1467997 c.7218+1G>A p.? Unknown 23:41229410-41229410 + TCGA-A5-A0VQ-01 COSM1155376 c.6269A>G p.H2090R Substitution - Missense 23:41218431-41218431 + TCGA-B5-A11E-01 COSM1121321 c.531C>A p.F177L Substitution - Missense 23:41136920-41136920 + PD24209a COSM5780975 c.593A>G p.D198G Substitution - Missense 23:41136982-41136982 + TCGA-BS-A0U8-01 COSM1155379 c.7442C>T p.A2481V Substitution - Missense 23:41229790-41229790 + HCC125 COSM1625889 c.4343G>A p.G1448D Substitution - Missense 23:41197494-41197494 + sysucc-1163T COSM5459510 c.2425A>G p.I809V Substitution - Missense 23:41168028-41168028 + PD8617a COSM5752445 c.419delG p.W140fs*1 Deletion - Frameshift 23:41134821-41134821 + TCGA-A6-5665-01 COSM1467961 c.2232A>C p.E744D Substitution - Missense 23:41166139-41166139 + TCGA-AA-3864-01 COSM272113 c.7410+2_7410+3insA p.? Unknown 23:41229781-41229782 + Pat_41_B COSM5877848 c.1198C>T p.P400S Substitution - Missense 23:41143348-41143348 + CG14 COSM5422878 c.6031C>G p.Q2011E Substitution - Missense 23:41216598-41216598 + ESCC_37 COSM5629003 c.2T>A p.M1K Substitution - Missense 23:41123630-41123630 + TCGA-AC-A2FM-01 COSM1599390 c.5331+1G>A p.? Unknown 23:41214710-41214710 + TCGA-HU-A4GQ-01 COSM4109496 c.6568G>A p.V2190M Substitution - Missense 23:41223219-41223219 + S02344 COSM5693963 c.6637G>C p.G2213R Substitution - Missense 23:41223288-41223288 + TCGA-AP-A056-01 COSM1599414 c.1252C>T p.R418C Substitution - Missense 23:41143381-41143381 + PT50 COSM5937923 c.6190C>T p.R2064C Substitution - Missense 23:41217324-41217324 + 082-02-1TD COSM146086 c.5725A>G p.M1909V Substitution - Missense 23:41216313-41216313 + S02139 COSM5674725 c.6333A>G p.K2111K Substitution - coding silent 23:41218516-41218516 + PD11367a COSM5752166 c.4548_4551delCAAA p.Q1518fs*1 Deletion - Frameshift 23:41198695-41198698 + 8031556 COSM3390631 c.131C>T p.P44L Substitution - Missense 23:41129034-41129034 + HCC2998 COSM2964873 c.5150C>T p.S1717F Substitution - Missense 23:41210643-41210643 + TCGA-AN-A0G0-01 COSM457505 c.6151C>G p.H2051D Substitution - Missense 23:41217306-41217306 + TCGA-AA-A010-01 COSM286413 c.5718C>T p.D1906D Substitution - coding silent 23:41216306-41216306 + 402 COSM4429870 c.7128_7129insT p.K2377fs*1 Insertion - Frameshift 23:41229319-41229320 + SNU-175 COSM1599410 c.1796G>A p.R599H Substitution - Missense 23:41152980-41152980 + TCGA-FS-A4F5-06 COSM3561687 c.5075C>T p.S1692L Substitution - Missense 23:41210568-41210568 + TCGA-EL-A3H5-01 COSM3372267 c.5372A>C p.K1791T Substitution - Missense 23:41215960-41215960 + TCGA-CK-4950-01 COSM1467955 c.968A>C p.N323T Substitution - Missense 23:41141184-41141184 + TCGA-39-5024-01 COSM1151641 c.6565+2T>A p.? Unknown 23:41219233-41219233 + pfg181T COSM4753515 c.1025A>G p.N342S Substitution - Missense 23:41141316-41141316 + 587376 COSM95500 c.184G>A p.D62N Substitution - Missense 23:41129087-41129087 + TCGA-DB-A4XD-01 COSM3973664 c.6874A>G p.T2292A Substitution - Missense 23:41224885-41224885 + PTC-88C COSM4156844 c.6702C>A p.V2234V Substitution - coding silent 23:41223374-41223374 + KPOPBR-40-T COSM5965970 c.3002A>G p.E1001G Substitution - Missense 23:41170594-41170594 + ZZUFHECRKL-G039T COSM5437774 c.3845T>A p.L1282* Substitution - Nonsense 23:41189364-41189364 + AML14 COSM3733118 c.1749G>A p.A583A Substitution - coding silent 23:41151043-41151043 + TBR08 COSM4168296 c.3429_3430insCAAC p.R1144fs*11 Insertion - Frameshift 23:41184546-41184547 + TCGA-D1-A177-01 COSM1121329 c.1486A>G p.M496V Substitution - Missense 23:41148456-41148456 + CHC1626T COSM4791651 c.1160A>G p.N387S Substitution - Missense 23:41143310-41143310 + Gp5D COSM2964866 c.4845A>G p.Q1615Q Substitution - coding silent 23:41205344-41205344 + HCC054T COSM5809614 c.5190T>C p.F1730F Substitution - coding silent 23:41214589-41214589 + TCGA-D1-A103-01 COSM187984 c.2524C>T p.R842* Substitution - Nonsense 23:41168127-41168127 + TCGA-66-2787-01 COSM1151635 c.2393C>T p.T798M Substitution - Missense 23:41167546-41167546 + T3724 COSM1121347 c.4075_4076delAG p.R1361fs*2 Deletion - Frameshift 23:41196601-41196602 + TCGA-AA-3663-01 COSM1467957 c.1654C>A p.L552I Substitution - Missense 23:41150969-41150969 + TCGA-BG-A0W1-01 COSM1121323 c.607C>G p.R203G Substitution - Missense 23:41136996-41136996 + HCC136T COSM5817150 c.3752G>T p.C1251F Substitution - Missense 23:41188059-41188059 + TCGA-A5-A0GW-01 COSM1155373 c.4748A>G p.N1583S Substitution - Missense 23:41201204-41201204 + B52-Tumor COSM1756565 c.2243A>C p.N748T Substitution - Missense 23:41166129-41166129 + TCGA-UB-A7ME-01 COSM4910205 c.5019T>A p.L1673L Substitution - coding silent 23:41210512-41210512 + TCGA-CK-5912-01 COSM1467996 c.7106_7107insT p.K2370fs*1 Insertion - Frameshift 23:41229318-41229319 + TCGA-G4-6628-01 COSM1467963 c.2729G>A p.R910Q Substitution - Missense 23:41170108-41170108 + TCGA-AX-A0J1-01 COSM1121371 c.6986_6987insT p.L2330fs*11 Insertion - Frameshift 23:41225083-41225084 + OV207 COSM252913 c.550C>T p.R184C Substitution - Missense 23:41136939-41136939 + ccRCC-27 COSM1664933 c.1138G>T p.A380S Substitution - Missense 23:41141429-41141429 + CSCC-30-T COSM4510067 c.805C>G p.L269V Substitution - Missense 23:41141021-41141021 + 345480 COSM3726284 c.3994G>T p.A1332S Substitution - Missense 23:41196267-41196267 + PCSI_0024_Pa_C COSM1232130 c.1112G>A p.R371Q Substitution - Missense 23:41141382-41141382 + TCGA-02-0047-01 COSM2149004 c.5599C>T p.Q1867* Substitution - Nonsense 23:41216187-41216187 + TCGA-AN-A0XN-01 COSM1134342 c.3881_3882insA p.C1295fs*13 Insertion - Frameshift 23:41189379-41189380 + DM101 COSM5611145 c.6395C>T p.S2132F Substitution - Missense 23:41218578-41218578 + ESCC_13 COSM5625406 c.7405G>C p.E2469Q Substitution - Missense 23:41229774-41229774 + WA12 COSM242209 c.5348C>T p.P1783L Substitution - Missense 23:41215936-41215936 + 082-02-1TD COSM1317250 c.5746A>G p.M1916V Substitution - Missense 23:41216313-41216313 + TCGA-CW-5581-01 COSM488367 c.6252C>A p.N2084K Substitution - Missense 23:41218435-41218435 + TCGA-A5-A0GP-01 COSM1121340 c.3112A>G p.K1038E Substitution - Missense 23:41171943-41171943 + 8044642 COSM3390636 c.3330C>G p.F1110L Substitution - Missense 23:41184468-41184468 + TCGA-BR-A4QL-01 COSM4109493 c.5954G>A p.R1985Q Substitution - Missense 23:41216542-41216542 + MDA-N COSM1683573 c.2755_2756insA p.I919fs*6 Insertion - Frameshift 23:41170113-41170114 + TCGA-AP-A051-01 COSM1121360 c.5848G>A p.D1950N Substitution - Missense 23:41216436-41216436 + TCGA-CM-6680-01 COSM1467952 c.460C>T p.R154C Substitution - Missense 23:41136828-41136828 + SNU-C4 COSM1599397 c.4096_4097delAG p.R1368fs*2 Deletion - Frameshift 23:41196601-41196602 + RKO COSM2964759 c.959G>T p.R320M Substitution - Missense 23:41141154-41141154 + DA2 COSM4167462 c.4550C>A p.T1517N Substitution - Missense 23:41198718-41198718 + DM10 COSM5611137 c.4651G>T p.G1551W Substitution - Missense 23:41201128-41201128 + TCGA-BR-8678-01 COSM4109489 c.5059G>A p.V1687M Substitution - Missense 23:41210573-41210573 + TCGA-AC-A23H-01 COSM3844687 c.283G>C p.E95Q Substitution - Missense 23:41131497-41131497 + TCGA-CM-5862-01 COSM1467998 c.7197+1G>A p.? Unknown 23:41229410-41229410 + TCGA-AC-A23H-01 COSM3844698 c.3873G>C p.L1291F Substitution - Missense 23:41189392-41189392 + RKO COSM2964760 c.938G>T p.R313M Substitution - Missense 23:41141154-41141154 + TCGA-A5-A0VQ-01 COSM1121364 c.6248A>G p.H2083R Substitution - Missense 23:41218431-41218431 + TCGA-BR-7851-01 COSM4109475 c.2586T>C p.H862H Substitution - coding silent 23:41168189-41168189 + TCGA-F4-6856-01 COSM270533 c.7410+3delA p.? Unknown 23:41229782-41229782 + TCGA-A7-A26J-01 COSM1490963 c.6565C>G p.L2189V Substitution - Missense 23:41223237-41223237 + 11114 COSM5751557 c.2398_2399insT p.N800fs*7 Insertion - Frameshift 23:41167572-41167573 + TCGA-AG-A002-01 COSM264633 c.6990G>T p.L2330F Substitution - Missense 23:41225087-41225087 + HCC086T COSM5813068 c.1942C>T p.Q648* Substitution - Nonsense 23:41162855-41162855 + MDA-N COSM1683574 c.2734_2735insA p.I912fs*6 Insertion - Frameshift 23:41170113-41170114 + TCGA-AR-A2LE-01 COSM3844689 c.1587C>T p.L529L Substitution - coding silent 23:41148536-41148536 + TCGA-DB-A4XD-01 COSM3973663 c.6895A>G p.T2299A Substitution - Missense 23:41224885-41224885 + TCGA-D7-6527-01 COSM4109490 c.5822G>A p.R1941H Substitution - Missense 23:41216389-41216389 + YUOMEGA COSM5412681 c.2807C>T p.P936L Substitution - Missense 23:41170186-41170186 + TCGA-AX-A060-01 COSM1599397 c.4096_4097delAG p.R1368fs*2 Deletion - Frameshift 23:41196601-41196602 + TCGA-CW-5581-01 COSM1138145 c.6273C>A p.N2091K Substitution - Missense 23:41218435-41218435 + DM45 COSM5611147 c.2310C>T p.V770V Substitution - coding silent 23:41167484-41167484 + TCGA-CZ-4861-01 COSM3364000 c.2196A>G p.L732L Substitution - coding silent 23:41166082-41166082 + TCGA-FU-A3HZ-01 COSM4840609 c.4008C>A p.F1336L Substitution - Missense 23:41196281-41196281 + ESCC_140 COSM5643470 c.3421A>G p.M1141V Substitution - Missense 23:41184538-41184538 + p2_III-1 COSM1738290 c.7054A>C p.T2352P Substitution - Missense 23:41225130-41225130 + CHC2099T COSM5347539 c.7686_7689delATCC p.S2563fs*>7 Deletion - Frameshift 23:41232497-41232500 + RK208_C01 COSM1636539 c.6277_6278insT p.N2095fs*1 Insertion - Frameshift 23:41218439-41218440 + TCGA-D3-A3C7-06 COSM3561694 c.7282C>T p.P2428S Substitution - Missense 23:41229651-41229651 + OSCC-GB_01090111 COSM4886506 c.423G>T p.K141N Substitution - Missense 23:41134825-41134825 + EGC15 COSM5064690 c.2779G>A p.V927I Substitution - Missense 23:41170137-41170137 + TCGA-AP-A0LM-01 COSM1121338 c.2855C>T p.S952L Substitution - Missense 23:41170234-41170234 + TCGA-F4-6570-01 COSM1467991 c.6623T>C p.V2208A Substitution - Missense 23:41223274-41223274 + TCGA-34-5929-01 COSM757277 c.4251G>C p.E1417D Substitution - Missense 23:41197402-41197402 + TCGA-A5-A0GH-01 COSM1121353 c.4733_4735delTTC p.L1579delL Deletion - In frame 23:41201210-41201212 + TCGA-HU-A4GQ-01 COSM4109480 c.3656T>C p.V1219A Substitution - Missense 23:41186614-41186614 + S01023 COSM5666883 c.2290G>A p.D764N Substitution - Missense 23:41166176-41166176 + TCGA-BR-8680-01 COSM4109465 c.955G>T p.E319* Substitution - Nonsense 23:41141171-41141171 + TCGA-BR-7851-01 COSM4109474 c.2607T>C p.H869H Substitution - coding silent 23:41168189-41168189 + PD3991a COSM165461 c.2175A>G p.L725L Substitution - coding silent 23:41166082-41166082 + TCGA-BR-4361-01 COSM4109467 c.1073T>C p.V358A Substitution - Missense 23:41141364-41141364 + T3090 COSM4739955 c.75_76insC p.L28fs*10 Insertion - Frameshift 23:41123703-41123704 + 2T COSM3713947 c.536A>G p.N179S Substitution - Missense 23:41136904-41136904 + CSCC-31-T COSM4496384 c.4719C>T p.S1573S Substitution - coding silent 23:41201196-41201196 + TCGA-BR-4368-01 COSM4109468 c.1897+2T>C p.? Unknown 23:41153083-41153083 + 11114 COSM5751556 c.2419_2420insT p.N807fs*7 Insertion - Frameshift 23:41167572-41167573 + TCGA-BR-6566-01 COSM4109471 c.1973T>C p.L658S Substitution - Missense 23:41165880-41165880 + PCSI_0024_Pa_C COSM1232131 c.1091G>A p.R364Q Substitution - Missense 23:41141382-41141382 + TCGA-A5-A0GB-01 COSM1121343 c.3284C>T p.A1095V Substitution - Missense 23:41184422-41184422 + pfg181T COSM2964734 c.76delC p.L28fs*51 Deletion - Frameshift 23:41123704-41123704 + S02284 COSM5684289 c.774A>G p.P258P Substitution - coding silent 23:41140969-41140969 + SJDOSTEOS013 COSM5760270 c.877G>A p.E293K Substitution - Missense 23:41141072-41141072 + TCGA-CJ-4875-01 COSM3363998 c.2154C>A p.D718E Substitution - Missense 23:41166040-41166040 + TCGA-AX-A0J1-01 COSM1599411 c.1657G>T p.D553Y Substitution - Missense 23:41150951-41150951 + TCGA-G4-6628-01 COSM1467962 c.2750G>A p.R917Q Substitution - Missense 23:41170108-41170108 + LOXIMVI COSM1683575 c.4600_4601insA p.T1534fs*4 Insertion - Frameshift 23:41198747-41198748 + TCGA-EE-A3J7-06 COSM3913994 c.85C>T p.Q29* Substitution - Nonsense 23:41123713-41123713 + SJTALL007 COSM4776552 c.2424+1G>C p.? Unknown 23:41167578-41167578 + TCGA-A8-A0A6-01 COSM3844703 c.5833T>G p.W1945G Substitution - Missense 23:41216400-41216400 + pfg181T COSM4765189 c.7434_7435insA p.A2481fs*17 Insertion - Frameshift 23:41229782-41229783 + TCGA-BR-8680-01 COSM4109464 c.976G>T p.E326* Substitution - Nonsense 23:41141171-41141171 + TCGA-BS-A0UV-01 COSM1599399 c.3758C>T p.S1253L Substitution - Missense 23:41188065-41188065 + MI4 COSM1145738 c.2249G>A p.R750Q Substitution - Missense 23:41166135-41166135 + TCGA-EJ-5517-01 COSM1132303 c.1107G>A p.E369E Substitution - coding silent 23:41141398-41141398 + 8047575 COSM3390633 c.1449A>G p.Q483Q Substitution - coding silent 23:41148398-41148398 + SW48 COSM2964909 c.6465C>T p.H2155H Substitution - coding silent 23:41219131-41219131 + B59 COSM1756570 c.6398C>T p.P2133L Substitution - Missense 23:41218581-41218581 + CSCC-17-T COSM4530855 c.1733G>C p.S578T Substitution - Missense 23:41151027-41151027 + TCGA-CJ-4875-01 COSM3363999 c.2133C>A p.D711E Substitution - Missense 23:41166040-41166040 + T3262 COSM4739963 c.7225G>T p.G2409* Substitution - Nonsense 23:41229573-41229573 + ESCC_37 COSM5629004 c.2T>A p.M1K Substitution - Missense 23:41123630-41123630 + 082 COSM146086 c.5725A>G p.M1909V Substitution - Missense 23:41216313-41216313 + TCGA-AB-2847-03 COSM1319439 c.4405C>A p.Q1469K Substitution - Missense 23:41198573-41198573 + TCGA-BP-4160-01 COSM3364002 c.3672A>G p.R1224R Substitution - coding silent 23:41188000-41188000 + TCGA-BF-A3DL-01 COSM4904967 c.6010C>T p.Q2004* Substitution - Nonsense 23:41216598-41216598 + OSCC-GB_00240111 COSM3713949 c.5062G>A p.E1688K Substitution - Missense 23:41210555-41210555 + PT09_2 COSM5895123 c.2616-1G>A p.? Unknown 23:41169994-41169994 + C0085T COSM4154953 c.2743C>T p.R915C Substitution - Missense 23:41170122-41170122 + pfg053T COSM4753536 c.5114G>C p.G1705A Substitution - Missense 23:41210607-41210607 + CRC-4 COSM304205 c.2164delC p.P722fs*4 Deletion - Frameshift 23:41166071-41166071 + PD11367a COSM5752167 c.4527_4530delCAAA p.Q1511fs*1 Deletion - Frameshift 23:41198695-41198698 + CHC1626T COSM4791650 c.1181A>G p.N394S Substitution - Missense 23:41143310-41143310 + TCGA-BH-A18U-01 COSM3844695 c.3876G>A p.M1292I Substitution - Missense 23:41189374-41189374 + TCGA-DA-A1HV-06 COSM3561687 c.5075C>T p.S1692L Substitution - Missense 23:41210568-41210568 + SC_9061 COSM5572209 c.1305G>C p.W435C Substitution - Missense 23:41143434-41143434 + Pat_46_A COSM5877851 c.6779G>A p.G2260D Substitution - Missense 23:41224769-41224769 + TCGA-FS-A4F5-06 COSM3561688 c.5054C>T p.S1685L Substitution - Missense 23:41210568-41210568 + TCGA-DM-A28M-01 COSM3694583 c.270G>T p.P90P Substitution - coding silent 23:41131484-41131484 + TCGA-AG-3878-01 COSM4739956 c.75_76insC p.L28fs*10 Insertion - Frameshift 23:41123703-41123704 + PD23564a COSM5752817 c.5851_5852insT p.Y1953fs*2 Insertion - Frameshift 23:41216418-41216419 + TCGA-EE-A2MR-06 COSM3561683 c.3985C>T p.R1329C Substitution - Missense 23:41196258-41196258 + TCGA-BR-4361-01 COSM4109484 c.4941T>C p.L1647L Substitution - coding silent 23:41205419-41205419 + TCGA-AP-A056-01 COSM1121326 c.1231C>T p.R411C Substitution - Missense 23:41143381-41143381 + tumor_4134005 COSM3357439 c.311T>C p.L104P Substitution - Missense 23:41131525-41131525 + TCGA-BR-8366-01 COSM4109473 c.2488A>G p.K830E Substitution - Missense 23:41168091-41168091 + TL67 COSM5752014 c.6594_6595insCTC p.F2198_M2199insL Insertion - In frame 23:41223266-41223267 + PD23564a COSM5752818 c.5830_5831insT p.Y1946fs*2 Insertion - Frameshift 23:41216418-41216419 + TCGA-CM-6165-01 COSM1467959 c.1877-1G>A p.? Unknown 23:41162789-41162789 + PD4264a COSM5793387 c.1450C>T p.R484C Substitution - Missense 23:41148399-41148399 + HCC2998 COSM4631913 c.1909T>G p.Y637D Substitution - Missense 23:41162801-41162801 + BD173T COSM5500303 c.7248C>T p.T2416T Substitution - coding silent 23:41229596-41229596 + PD11367a COSM5752166 c.4548_4551delCAAA p.Q1518fs*1 Deletion - Frameshift 23:41198695-41198698 + TCGA-EE-A3AF-06 COSM3561673 c.1589G>A p.S530N Substitution - Missense 23:41148538-41148538 + ML3 COSM1165519 c.2313G>A p.V771V Substitution - coding silent 23:41167487-41167487 + TCGA-AX-A0J0-01 COSM1599386 c.6084C>T p.P2028P Substitution - coding silent 23:41216651-41216651 + RK072_C01 COSM1636538 c.6200T>A p.L2067* Substitution - Nonsense 23:41218383-41218383 + TL67 COSM5752013 c.6615_6616insCTC p.F2205_M2206insL Insertion - In frame 23:41223266-41223267 + 587284 COSM1232128 c.2143A>G p.S715G Substitution - Missense 23:41166050-41166050 + TCGA-CG-5721-01 COSM4109458 c.376A>C p.I126L Substitution - Missense 23:41134778-41134778 + TCGA-AP-A056-01 COSM1121320 c.530T>G p.F177C Substitution - Missense 23:41136919-41136919 + DA2 COSM4167461 c.4571C>A p.T1524N Substitution - Missense 23:41198718-41198718 + B21-Tumor COSM4005081 c.1504G>A p.V502M Substitution - Missense 23:41148453-41148453 + sysucc-1163T COSM5459509 c.2446A>G p.I816V Substitution - Missense 23:41168028-41168028 + DM10 COSM5611136 c.4672G>T p.G1558W Substitution - Missense 23:41201128-41201128 + TL42 COSM5751869 c.3755G>AG p.G1252fs*8 Complex - frameshift 23:41188062-41188062 + TCGA-DB-A64L-01 COSM3973661 c.5440G>A p.D1814N Substitution - Missense 23:41216007-41216007 + TCGA-FS-A1ZK-06 COSM3561689 c.5339C>T p.T1780I Substitution - Missense 23:41215906-41215906 + 112533 COSM95688 c.2794G>T p.E932* Substitution - Nonsense 23:41170173-41170173 + TCGA-B5-A0K9-01 COSM1155365 c.420G>A p.W140* Substitution - Nonsense 23:41134822-41134822 + p2_VI-2 COSM1738291 c.7033A>C p.T2345P Substitution - Missense 23:41225130-41225130 + RK072_C01 COSM1636537 c.6221T>A p.L2074* Substitution - Nonsense 23:41218383-41218383 + T3298 COSM4739958 c.2443C>A p.R815S Substitution - Missense 23:41168046-41168046 + pfg043T COSM4753528 c.3183T>G p.C1061W Substitution - Missense 23:41184032-41184032 + DM10 COSM5611142 c.644G>T p.R215L Substitution - Missense 23:41137012-41137012 + CSCC-15-T COSM1599399 c.3758C>T p.S1253L Substitution - Missense 23:41188065-41188065 + TCGA-HU-A4G6-01 COSM4109463 c.729A>G p.Q243Q Substitution - coding silent 23:41140751-41140751 + TCGA-AA-A00N-01 COSM278054 c.3550A>G p.T1184A Substitution - Missense 23:41186529-41186529 + LOVO COSM1121370 c.6876C>T p.T2292T Substitution - coding silent 23:41224887-41224887 + LOXIMVI COSM1683576 c.4579_4580insA p.T1527fs*4 Insertion - Frameshift 23:41198747-41198748 + ESCC_13 COSM5625405 c.7426G>C p.E2476Q Substitution - Missense 23:41229774-41229774 + TCGA-A3-3370-01 COSM1138149 c.7657C>G p.Q2553E Substitution - Missense 23:41232468-41232468 + TCGA-B9-5156-01 COSM3992475 c.649C>A p.L217I Substitution - Missense 23:41140671-41140671 + TCGA-AA-A00N-01 COSM278055 c.3710A>C p.K1237T Substitution - Missense 23:41188038-41188038 + TCGA-CA-6718-01 COSM1467973 c.5042A>C p.E1681A Substitution - Missense 23:41210556-41210556 + TCGA-JW-A852-01 COSM4823794 c.3304G>A p.D1102N Substitution - Missense 23:41184442-41184442 + TCGA-A5-A0GB-01 COSM1155372 c.3305C>T p.A1102V Substitution - Missense 23:41184422-41184422 + TCGA-HU-A4GT-01 COSM4109495 c.6325T>C p.F2109L Substitution - Missense 23:41218508-41218508 + TCGA-JW-A852-01 COSM4823793 c.3325G>A p.D1109N Substitution - Missense 23:41184442-41184442 + TCGA-BH-A18G-01 COSM1599397 c.4096_4097delAG p.R1368fs*2 Deletion - Frameshift 23:41196601-41196602 + TCGA-AP-A059-01 COSM1599381 c.6850A>C p.S2284R Substitution - Missense 23:41224840-41224840 + TCGA-BR-7707-01 COSM4109498 c.7440A>G p.K2480K Substitution - coding silent 23:41229788-41229788 + S00944 COSM5664351 c.2115G>A p.M705I Substitution - Missense 23:41166001-41166001 + CSCC-11-T COSM4450638 c.7480-1G>A p.? Unknown 23:41230500-41230500 + SW620 COSM2964895 c.5772G>C p.E1924D Substitution - Missense 23:41216339-41216339 + TCGA-AG-A026-01 COSM290549 c.1449G>A p.L483L Substitution - coding silent 23:41148419-41148419 + TCGA-AZ-6598-01 COSM1467946 c.31G>A p.G11R Substitution - Missense 23:41123659-41123659 + TCGA-AN-A046-01 COSM3844692 c.1623G>T p.K541N Substitution - Missense 23:41150938-41150938 + OSCC-GB_00940111 COSM4891674 c.3936G>T p.W1312C Substitution - Missense 23:41189434-41189434 + SW48 COSM2964910 c.6444C>T p.H2148H Substitution - coding silent 23:41219131-41219131 + TCGA-B0-4712-01 COSM1138147 c.6973-1G>T p.? Unknown 23:41225048-41225048 + TCGA-HU-A4H3-01 COSM4109486 c.5041C>T p.R1681C Substitution - Missense 23:41210534-41210534 + 3N60-VS-3T60 COSM4984352 c.3794A>G p.N1265S Substitution - Missense 23:41189313-41189313 + YUJUBE COSM5412682 c.5673T>C p.D1891D Substitution - coding silent 23:41216240-41216240 + TCGA-D1-A165-01 COSM1121357 c.5338A>T p.K1780* Substitution - Nonsense 23:41215926-41215926 + TCGA-E9-A1RF-01 COSM1490957 c.3479C>G p.T1160S Substitution - Missense 23:41184596-41184596 + SNUH_G65_S1 COSM4420206 c.5424T>C p.C1808C Substitution - coding silent 23:41215991-41215991 + DM55 COSM5611149 c.5195C>T p.T1732I Substitution - Missense 23:41214594-41214594 + REC-1 COSM1740816 c.7151C>T p.A2384V Substitution - Missense 23:41229342-41229342 + B80-Tumor COSM1756568 c.2952T>C p.G984G Substitution - coding silent 23:41170565-41170565 + OSCC-GB_00010111 COSM1636542 c.6263A>G p.N2088S Substitution - Missense 23:41218446-41218446 + CHC1603T COSM4801831 c.4150A>G p.I1384V Substitution - Missense 23:41196676-41196676 + TCGA-HU-A4GQ-01 COSM4109497 c.6547G>A p.V2183M Substitution - Missense 23:41223219-41223219 + TCGA-39-5024-01 COSM757272 c.6544+2T>A p.? Unknown 23:41219233-41219233 + TCGA-BS-A0UV-01 COSM1121345 c.3737C>T p.S1246L Substitution - Missense 23:41188065-41188065 + 2250198 COSM5030708 c.4447_4448insT p.P1483fs*10 Insertion - Frameshift 23:41198615-41198616 + RK071_C01 COSM1636543 c.6585G>A p.Q2195Q Substitution - coding silent 23:41223236-41223236 + HCC136T COSM5817151 c.3731G>T p.C1244F Substitution - Missense 23:41188059-41188059 + HCC084T COSM3844697 c.3894G>C p.L1298F Substitution - Missense 23:41189392-41189392 + TCGA-BR-8078-01 COSM4109492 c.5975G>A p.R1992Q Substitution - Missense 23:41216542-41216542 + RK071_C01 COSM1636544 c.6564G>A p.Q2188Q Substitution - coding silent 23:41223236-41223236 + TCGA-BT-A3PK-01 COSM3800599 c.5912A>G p.E1971G Substitution - Missense 23:41216479-41216479 + PT50 COSM5937921 c.6232C>T p.L2078F Substitution - Missense 23:41218394-41218394 + CHC1626T COSM4791651 c.1160A>G p.N387S Substitution - Missense 23:41143310-41143310 + PT09_1 COSM5895123 c.2616-1G>A p.? Unknown 23:41169994-41169994 + 9-RS COSM1731895 c.6172G>T p.G2058C Substitution - Missense 23:41217327-41217327 + 2215528 COSM1145742 c.5015G>T p.R1672M Substitution - Missense 23:41205493-41205493 + B52-Tumor COSM1756566 c.2222A>C p.N741T Substitution - Missense 23:41166129-41166129 + p2_VI-1 COSM1738291 c.7033A>C p.T2345P Substitution - Missense 23:41225130-41225130 + STC232 COSM2964734 c.76delC p.L28fs*51 Deletion - Frameshift 23:41123704-41123704 + 345480 COSM3726285 c.3973G>T p.A1325S Substitution - Missense 23:41196267-41196267 + TCGA-BR-4292-01 COSM4109461 c.573A>G p.S191S Substitution - coding silent 23:41136962-41136962 + 27 COSM5748850 c.4030_4031insCTTTT p.L1344fs*31 Insertion - Frameshift 23:41196324-41196325 + HCC65T COSM1625891 c.4359+2T>A p.? Unknown 23:41197512-41197512 + TCGA-D5-6538-01 COSM1467982 c.5831delT p.Y1946fs*7 Deletion - Frameshift 23:41216419-41216419 + H1155 COSM1195858 c.712C>T p.H238Y Substitution - Missense 23:41140713-41140713 + 107850 COSM96275 c.4656G>A p.L1552L Substitution - coding silent 23:41201133-41201133 + OSCC-GB_01070111 COSM4889378 c.1219G>T p.E407* Substitution - Nonsense 23:41143369-41143369 + PT23_1 COSM5903301 c.3663+2T>C p.? Unknown 23:41186644-41186644 + TCGA-AG-3891-01 COSM5068649 c.75_76insCC p.L28fs*52 Insertion - Frameshift 23:41123703-41123704 + HN_62995 COSM130132 c.1514G>T p.W505L Substitution - Missense 23:41148484-41148484 + TCGA-66-2763-01 COSM757280 c.902C>A p.S301* Substitution - Nonsense 23:41141118-41141118 + TCGA-AC-A23H-01 COSM3844688 c.283G>C p.E95Q Substitution - Missense 23:41131497-41131497 + SNUH_G65_S1 COSM4420207 c.5403T>C p.C1801C Substitution - coding silent 23:41215991-41215991 + TCGA-CK-4950-01 COSM1467954 c.989A>C p.N330T Substitution - Missense 23:41141184-41141184 + 22T COSM3713901 c.1763+1G>T p.? Unknown 23:41151058-41151058 + T23 COSM1599396 c.4119C>T p.G1373G Substitution - coding silent 23:41196624-41196624 + TCGA-B5-A11E-01 COSM1599418 c.552C>A p.F184L Substitution - Missense 23:41136920-41136920 + TCGA-34-5929-01 COSM1151638 c.4987G>C p.V1663L Substitution - Missense 23:41205465-41205465 + TCGA-13-2071-01 COSM1331873 c.186T>A p.D62E Substitution - Missense 23:41129089-41129089 + 103447 COSM95501 c.3672A>T p.R1224S Substitution - Missense 23:41188000-41188000 + TCGA-D1-A177-01 COSM1155368 c.1507A>G p.M503V Substitution - Missense 23:41148456-41148456 + TCGA-B5-A11J-01 COSM1599420 c.285A>G p.E95E Substitution - coding silent 23:41131499-41131499 + TCGA-EE-A2MR-06 COSM3561676 c.2650C>T p.R884* Substitution - Nonsense 23:41170029-41170029 + TCGA-D9-A148-06 COSM3561671 c.1111C>T p.R371* Substitution - Nonsense 23:41141381-41141381 + LUAD-B00915 COSM355741 c.7444G>T p.E2482* Substitution - Nonsense 23:41230534-41230534 + 402 COSM4429871 c.7107_7108insT p.K2370fs*1 Insertion - Frameshift 23:41229319-41229320 + T3298 COSM4739957 c.2464C>A p.R822S Substitution - Missense 23:41168046-41168046 + TCGA-EA-A439-01 COSM4843713 c.5683G>A p.D1895N Substitution - Missense 23:41216271-41216271 + ESCC_107 COSM5650075 c.3028-5_3028-2delTCTA p.? Unknown 23:41171833-41171836 + TCGA-F5-6814-01 COSM3424793 c.4254G>T p.T1418T Substitution - coding silent 23:41197405-41197405 + T3720 COSM4739959 c.2513_2514delAC p.D838fs*3 Deletion - Frameshift 23:41168095-41168096 + BRC13 COSM5028895 c.2122G>A p.E708K Substitution - Missense 23:41166008-41166008 + TCGA-AA-3713-01 COSM1467987 c.6246G>T p.K2082N Substitution - Missense 23:41218408-41218408 + TCGA-B9-5156-01 COSM3992474 c.670C>A p.L224I Substitution - Missense 23:41140671-41140671 + TCGA-AX-A1C8-01 COSM1121354 c.5242G>A p.E1748K Substitution - Missense 23:41214641-41214641 + CSB1 COSM5028898 c.5778G>A p.M1926I Substitution - Missense 23:41216366-41216366 + TCGA-CC-A3M9-01 COSM4928412 c.1761C>T p.P587P Substitution - coding silent 23:41152966-41152966 + YUJUBE COSM5412679 c.2003C>T p.P668L Substitution - Missense 23:41165910-41165910 + TCGA-FW-A3R5-06 COSM3561684 c.3964C>T p.R1322C Substitution - Missense 23:41196258-41196258 + TCGA-BR-7707-01 COSM4109499 c.7410+9A>G p.? Unknown 23:41229788-41229788 + TCGA-AP-A0LM-01 COSM1599404 c.2876C>T p.S959L Substitution - Missense 23:41170234-41170234 + RK071_C01 COSM1636545 c.6586C>T p.L2196F Substitution - Missense 23:41223237-41223237 + PD4264a COSM5793388 c.1429C>T p.R477C Substitution - Missense 23:41148399-41148399 + MD-285 COSM303536 c.4202A>G p.K1401R Substitution - Missense 23:41196728-41196728 + DM101 COSM5611144 c.6416C>T p.S2139F Substitution - Missense 23:41218578-41218578 + BK0047D COSM4187867 c.157C>T p.Q53* Substitution - Nonsense 23:41129060-41129060 + PD24209a COSM5780974 c.614A>G p.D205G Substitution - Missense 23:41136982-41136982 + TCGA-D1-A176-01 COSM1155378 c.6744A>G p.S2248S Substitution - coding silent 23:41223395-41223395 + TCGA-AC-A2FM-01 COSM1121356 c.5310+1G>A p.? Unknown 23:41214710-41214710 + KPOPBR-40-T COSM5965971 c.2981A>G p.E994G Substitution - Missense 23:41170594-41170594 + 24T COSM3713949 c.5062G>A p.E1688K Substitution - Missense 23:41210555-41210555 + DM10 COSM5611139 c.5475C>A p.V1825V Substitution - coding silent 23:41216063-41216063 + ZZUFHECRKL-G039T COSM5437773 c.3866T>A p.L1289* Substitution - Nonsense 23:41189364-41189364 + TCGA-C8-A26Y-01 COSM3844694 c.3784G>C p.E1262Q Substitution - Missense 23:41188112-41188112 + sysucc-783T COSM5485161 c.4573G>A p.A1525T Substitution - Missense 23:41198741-41198741 + PD11374a COSM5767368 c.1369C>G p.Q457E Substitution - Missense 23:41144597-41144597 + RK176_C01 COSM3766942 c.7372G>T p.E2458* Substitution - Nonsense 23:41229720-41229720 + TCGA-61-1900-01 COSM1331869 c.1033A>G p.M345V Substitution - Missense 23:41141324-41141324 + TCGA-AG-3892-01 COSM258342 c.514A>C p.N172H Substitution - Missense 23:41136903-41136903 + PT23_1 COSM5903300 c.3684+2T>C p.? Unknown 23:41186644-41186644 + TCGA-CC-A3MA-01 COSM4942921 c.7398A>G p.T2466T Substitution - coding silent 23:41229746-41229746 + TCGA-AA-3713-01 COSM1467988 c.6225G>T p.K2075N Substitution - Missense 23:41218408-41218408 + tumor_4133263 COSM5947821 c.6351A>G p.A2117A Substitution - coding silent 23:41218513-41218513 + 112503 COSM95500 c.184G>A p.D62N Substitution - Missense 23:41129087-41129087 + 2215529 COSM1145742 c.5015G>T p.R1672M Substitution - Missense 23:41205493-41205493 + TCGA-D3-A2JO-06 COSM3561692 c.5643T>C p.N1881N Substitution - coding silent 23:41216231-41216231 + Pat_41_B COSM5877849 c.2453C>T p.S818F Substitution - Missense 23:41168035-41168035 + S02139 COSM5674724 c.6354A>G p.K2118K Substitution - coding silent 23:41218516-41218516 + TCGA-HU-A4GQ-01 COSM4109481 c.3635T>C p.V1212A Substitution - Missense 23:41186614-41186614 + TCGA-AP-A051-01 COSM1599396 c.4119C>T p.G1373G Substitution - coding silent 23:41196624-41196624 + PT46 COSM5930170 c.7523C>T p.P2508L Substitution - Missense 23:41230544-41230544 + B59 COSM1756569 c.6419C>T p.P2140L Substitution - Missense 23:41218581-41218581 + PD11374a COSM5767367 c.1390C>G p.Q464E Substitution - Missense 23:41144597-41144597 + TCGA-AN-A0G0-01 COSM1134343 c.6172C>G p.H2058D Substitution - Missense 23:41217306-41217306 + TCGA-G4-6588-01 COSM1467993 c.6854A>G p.Y2285C Substitution - Missense 23:41224844-41224844 + TCGA-61-1727-01 COSM1331871 c.266T>G p.L89W Substitution - Missense 23:41131480-41131480 + TL41 COSM5751801 c.5879G>AG p.R1960fs*22 Complex - frameshift 23:41216467-41216467 + TCGA-AZ-4315-01 COSM1468000 c.7557G>T p.M2519I Substitution - Missense 23:41232437-41232437 + H1155 COSM1195399 c.5594G>A p.S1865N Substitution - Missense 23:41216182-41216182 + TCGA-F4-6856-01 COSM1644032 c.7434delA p.A2481fs*7 Deletion - Frameshift 23:41229782-41229782 + RK022_C01 COSM1636535 c.1885C>A p.L629I Substitution - Missense 23:41153069-41153069 + Pat_16_B COSM3561676 c.2650C>T p.R884* Substitution - Nonsense 23:41170029-41170029 + CHC2113T COSM5347537 c.1061_1076del16 p.A354fs*3 Deletion - Frameshift 23:41141331-41141346 + ESO-887 COSM1270121 c.6960A>T p.E2320D Substitution - Missense 23:41224950-41224950 + TCGA-CM-5864-01 COSM1467969 c.4418A>C p.N1473T Substitution - Missense 23:41198586-41198586 + YUOMEGA COSM5412680 c.2828C>T p.P943L Substitution - Missense 23:41170186-41170186 + RK208_C01 COSM1636542 c.6263A>G p.N2088S Substitution - Missense 23:41218446-41218446 + TCGA-D9-A6EC-06 COSM4401508 c.3866T>C p.F1289S Substitution - Missense 23:41189385-41189385 + S02384 COSM5698677 c.6841G>T p.V2281L Substitution - Missense 23:41224831-41224831 + TCGA-F4-6570-01 COSM1467992 c.6602T>C p.V2201A Substitution - Missense 23:41223274-41223274 + HCC125T COSM1625888 c.4364G>A p.G1455D Substitution - Missense 23:41197494-41197494 + p2_VI-1 COSM1738290 c.7054A>C p.T2352P Substitution - Missense 23:41225130-41225130 + TCGA-B5-A11N-01 COSM1121358 c.5475C>T p.V1825V Substitution - coding silent 23:41216063-41216063 + 6115115 COSM5547830 c.7027_7028delTG p.W2343fs*7 Deletion - Frameshift 23:41225124-41225125 + p2_VI-3 COSM1738291 c.7033A>C p.T2345P Substitution - Missense 23:41225130-41225130 + T3021 COSM272113 c.7410+2_7410+3insA p.? Unknown 23:41229781-41229782 + SJHGG053_A COSM1599407 c.2545C>T p.R849* Substitution - Nonsense 23:41168127-41168127 + 0078_CRUK_PC_0078_T1_DNA COSM4420807 c.3920G>A p.S1307N Substitution - Missense 23:41189418-41189418 + B80 COSM1756568 c.2952T>C p.G984G Substitution - coding silent 23:41170565-41170565 + TCGA-G4-6628-01 COSM1467948 c.194C>A p.P65H Substitution - Missense 23:41129097-41129097 + TCGA-A6-6650-01 COSM3694585 c.5532G>T p.E1844D Substitution - Missense 23:41216120-41216120 + 46T COSM3713951 c.7258G>T p.E2420* Substitution - Nonsense 23:41229606-41229606 + 587376 COSM1232129 c.184G>A p.D62N Substitution - Missense 23:41129087-41129087 + p2_I-2 COSM1738291 c.7033A>C p.T2345P Substitution - Missense 23:41225130-41225130 + TARGET-20-PAMYAS-04A-01D COSM5487465 c.6358_6359insGGCCT p.I2120fs*3 Insertion - Frameshift 23:41218520-41218521 + CHC2099T COSM5347540 c.7617_7620delATCC p.S2540fs*>7 Deletion - Frameshift 23:41232497-41232500 + ME043T COSM228765 c.5434C>T p.P1812S Substitution - Missense 23:41216022-41216022 + DM59 COSM5611150 c.4006T>C p.F1336L Substitution - Missense 23:41196279-41196279 + LUAD-S01346 COSM405119 c.601_602delTT p.F201fs*31 Deletion - Frameshift 23:41136990-41136991 + pfg016T COSM270533 c.7410+3delA p.? Unknown 23:41229782-41229782 + Pat_16_B COSM3561675 c.2671C>T p.R891* Substitution - Nonsense 23:41170029-41170029 + S02344 COSM5693964 c.6616G>C p.G2206R Substitution - Missense 23:41223288-41223288 + 2250198 COSM5030707 c.4468_4469insT p.P1490fs*10 Insertion - Frameshift 23:41198615-41198616 + LUAD-NYU627 COSM375491 c.7402C>A p.P2468T Substitution - Missense 23:41229771-41229771 + TCGA-B5-A0JY-01 COSM1121342 c.3138G>A p.T1046T Substitution - coding silent 23:41184008-41184008 + 1N64-VS-1T64 COSM4978100 c.918_924delTTTGAAG p.L307fs*2 Deletion - Frameshift 23:41141134-41141140 + TCGA-AX-A0J1-01 COSM1599396 c.4119C>T p.G1373G Substitution - coding silent 23:41196624-41196624 + S02284 COSM5684290 c.753A>G p.P251P Substitution - coding silent 23:41140969-41140969 + OSCC-GB_00220111 COSM3713902 c.1742+1G>T p.? Unknown 23:41151058-41151058 + TCGA-B5-A11N-01 COSM1121335 c.2623C>T p.R875C Substitution - Missense 23:41170002-41170002 + TCGA-BS-A0UF-01 COSM1599414 c.1252C>T p.R418C Substitution - Missense 23:41143381-41143381 + TCGA-D1-A101-01 COSM1121319 c.524G>A p.C175Y Substitution - Missense 23:41136913-41136913 + PD13802a COSM5025054 c.328G>C p.D110H Substitution - Missense 23:41134730-41134730 + p2_VI-3 COSM1738290 c.7054A>C p.T2352P Substitution - Missense 23:41225130-41225130 + pfg068T COSM4753510 c.13A>G p.T5A Substitution - Missense 23:41123641-41123641 + TCGA-A3-3370-01 COSM488371 c.7588C>G p.Q2530E Substitution - Missense 23:41232468-41232468 + TCGA-AP-A0LM-01 COSM1599385 c.6153C>A p.F2051L Substitution - Missense 23:41217287-41217287 + TCGA-BT-A0YX-01 COSM422566 c.6227A>T p.N2076I Substitution - Missense 23:41218410-41218410 + TCGA-B5-A11E-01 COSM1121328 c.1398+2T>G p.? Unknown 23:41144628-41144628 + ESCC-185T COSM3939992 c.1606C>T p.L536L Substitution - coding silent 23:41148555-41148555 + TL68 COSM5752025 c.966_967insGGGT p.N323fs*2 Insertion - Frameshift 23:41141182-41141183 + MDA-MB-435 COSM1682561 c.944C>T p.P315L Substitution - Missense 23:41141160-41141160 + TCGA-CM-6165-01 COSM1467958 c.1898-1G>A p.? Unknown 23:41162789-41162789 + TCGA-D8-A1X7-01 COSM1490954 c.2248C>T p.R750* Substitution - Nonsense 23:41166134-41166134 + 07-058 COSM3736498 c.1867T>C p.Y623H Substitution - Missense 23:41153051-41153051 + C547 COSM1599406 c.2644C>T p.R882C Substitution - Missense 23:41170002-41170002 + TCGA-AP-A059-01 COSM1121366 c.6403C>T p.P2135S Substitution - Missense 23:41218586-41218586 + TCGA-CM-6680-01 COSM1467953 c.443-4C>T p.? Unknown 23:41136828-41136828 + 112287 COSM95502 c.6338T>C p.I2113T Substitution - Missense 23:41218521-41218521 + pfg053T COSM4753537 c.5093G>C p.G1698A Substitution - Missense 23:41210607-41210607 + PT46 COSM5930171 c.7454C>T p.P2485L Substitution - Missense 23:41230544-41230544 + MN-105 COSM1578639 c.5181C>T p.C1727C Substitution - coding silent 23:41210674-41210674 + ESCC-185T COSM3939993 c.1585C>T p.L529L Substitution - coding silent 23:41148555-41148555 + ESO-887 COSM1270122 c.6939A>T p.E2313D Substitution - Missense 23:41224950-41224950 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.77578 Xp11.4 300072

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer AAG - InFrameDeletion p.R2429delR c.7285_7287delAGA X 41088882 LGG ACA - InFrameDeletion p.N2441delN c.7320_7322delCAA X 41088917 HNSC A C Missense p.K1798T c.5393A>C X 41075213 THCA A - Frameshift p.A2481Pfs*7 c.7440delA X 41089035 STAD - A Frameshift p.C1295Mfs*13 c.3882dupA X 41048633 BRCA - A Frameshift p.P1105Tfs*4 c.3312dupA X 41043682 THCA - A Frameshift p.S2319Kfs*2 c.6955dupA X 41084198 BRCA AG - Frameshift p.E93Ifs*10 c.273_274delAG X 40990740 BRCA AG - Frameshift p.R1368Sfs*2 c.4104_4105delAG X 41055854 UCEC A G Missense p.D1912G c.5735A>G X 41075555 OV A G Missense p.D239G c.716A>G X 40999970 PRAD A G Missense p.E1971G c.5912A>G X 41075732 BLCA A G Missense p.H2090R c.6269A>G X 41077684 UCEC A G Missense p.H370R c.1109A>G X 41000632 HNSC A G Missense p.K1045E c.3133A>G X 41031196 UCEC A G Missense p.M1916V c.5746A>G X 41075566 CLL A G Missense p.M503V c.1507A>G X 41007709 UCEC A G Missense p.N1583S c.4748A>G X 41060457 UCEC A G Missense p.N300S c.899A>G X 41000347 LUAD A G Missense p.S787G c.2359A>G X 41026765 STAD A G Missense p.T911A c.2731A>G X 41029342 UCEC A G Synonymous p.E95E c.285A>G X 40990752 UCEC A G Synonymous p.K1773K c.5319A>G X 41073950 THCA A G Synonymous p.L629L c.1887A>G X 41012324 LUAD A G Synonymous p.L732L c.2196A>G X 41025335 BRCA A G Synonymous p.L732L c.2196A>G X 41025335 RCCC A G Synonymous p.R1231R c.3693A>G X 41047253 RCCC A G Synonymous p.S198S c.594A>G X 40996215 STAD A - IntronicDeletion . c.6752-89delA X 41083898 ESCA A T Missense p.E1634V c.4901A>T X 41064632 MM A T Missense p.E2320D c.6960A>T X 41084203 ESCA A T Missense p.I790L c.2368A>T X 41026774 CM A T Missense p.N2083I c.6248A>T X 41077663 BLCA A T Synonymous p.S1985S c.5955A>T X 41075775 LUSC CACAATC - Frameshift p.T2372Sfs*15 c.7115_7121delCAATCCA X 41088557 HNSC C A Missense p.A2384E c.7151C>A X 41088595 RCCC C A Missense p.D718E c.2154C>A X 41025293 RCCC C A Missense p.L629I c.1885C>A X 41012322 HC C A Nonsense p.S308* c.923C>A X 41000371 LUSC C A Synonymous p.P568P c.1704C>A X 41010251 STAD - CG Frameshift p.V853Rfs*3 c.2556_2557insCG X 41027391 AML C G Missense p.H2058D c.6172C>G X 41076559 BRCA C G Missense p.H2090D c.6268C>G X 41077683 BRCA C G Missense p.L2196V c.6586C>G X 41082490 BRCA C G Missense p.P1048R c.3143C>G X 41031206 HNSC C G Missense p.Q2553E c.7657C>G X 41091721 RCCC C G Missense p.R1348G c.4042C>G X 41055568 CM C G Missense p.R210G c.628C>G X 40996249 UCEC C G Missense p.T1160S c.3479C>G X 41043849 BRCA C T 3-UTRSNV . c.7710+25C>T X 41091799 CM C T Missense p.A1102V c.3305C>T X 41043675 UCEC C T Missense p.A1538V c.4613C>T X 41060322 MB C T Missense p.A1768V c.5303C>T X 41073934 UCEC C T Missense p.A2481V c.7442C>T X 41089043 UCEC C T Missense p.A56V c.167C>T X 40988323 HNSC C T Missense p.P1105L c.3314C>T X 41043684 HNSC C T Missense p.P1819S c.5455C>T X 41075275 CM C T Missense p.P2435S c.7303C>T X 41088904 CM C T Missense p.P802L c.2405C>T X 41026811 CM C T Missense p.P973S c.2917C>T X 41029762 LUAD C T Missense p.R2079C c.6235C>T X 41077650 BRCA C T Missense p.S1692L c.5075C>T X 41069821 CM C T Missense p.S959L c.2876C>T X 41029487 CM C T Missense p.T1053M c.3158C>T X 41043260 BRCA C T Missense p.T1780I c.5339C>T X 41075159 CM C T Missense p.T798M c.2393C>T X 41026799 LUSC C T Nonsense p.Q1874* c.5620C>T X 41075440 GBM C T Nonsense p.Q2011* c.6031C>T X 41075851 CM C T Nonsense p.Q2436* c.7306C>T X 41088907 LUAD C T Nonsense p.Q29* c.85C>T X 40982966 CM C T Nonsense p.Q30* c.88C>T X 40982969 CM C T Nonsense p.R371* c.1111C>T X 41000634 CM C T Nonsense p.R750* c.2248C>T X 41025387 BRCA C T Synonymous p.A1097A c.3291C>T X 41043661 LUAD C T Synonymous p.D1281D c.3843C>T X 41048594 HNSC C T Synonymous p.D601D c.1803C>T X 41012240 BRCA C T Synonymous p.G1511G c.4533C>T X 41057933 UCEC C T Synonymous p.I2043I c.6129C>T X 41076516 PAAD G A Missense p.A2138T c.6412G>A X 41077827 HNSC G A Missense p.D1902N c.5704G>A X 41075524 LUAD G A Missense p.E1755K c.5263G>A X 41073894 UCEC G A Missense p.E357K c.1069G>A X 41000592 HNSC G A Missense p.E708K c.2122G>A X 41025261 BRCA G A Missense p.M1933I c.5799G>A X 41075619 BRCA G A Missense p.M1999I c.5997G>A X 41075817 LUAD G A Missense p.M705I c.2115G>A X 41025254 SCLC G A Missense p.R1783H c.5348G>A X 41075168 HNSC G A Missense p.R1941H c.5822G>A X 41075642 STAD G A Missense p.R742Q c.2225G>A X 41025364 BRCA G A Missense p.R750Q c.2249G>A X 41025388 LUAD G A Missense p.S530N c.1589G>A X 41007791 CM G A Missense p.V1491I c.4471G>A X 41057871 CM G A Missense p.V1781I c.5341G>A X 41075161 CM G A Nonsense p.W140* c.420G>A X 40994075 UCEC G A SpliceAcceptorSNV . c.2329-1G>A X 41026734 HNSC G A Synonymous p.A583A c.1749G>A X 41010296 AML G A Synonymous p.E376E c.1128G>A X 41000651 PRAD G A Synonymous p.L2128L c.6384G>A X 41077799 HNSC G A Synonymous p.L490L c.1470G>A X 41007672 COREAD G A Synonymous p.L508L c.1524G>A X 41007726 LUAD G A Synonymous p.V1868V c.5604G>A X 41075424 GBM G C Missense p.A569P c.1705G>C X 41010252 LUSC G C Missense p.C1920S c.5759G>C X 41075579 GBM G C Missense p.D1962H c.5884G>C X 41075704 HNSC G C Missense p.D1963H c.5887G>C X 41075707 LUAD G C Missense p.E1424D c.4272G>C X 41056655 LUSC G C Missense p.E379Q c.1135G>C X 41000658 LUAD G C Missense p.G883A c.2648G>C X 41029259 STAD G C Missense p.R1144P c.3431G>C X 41043801 ALL G C Missense p.V1663L c.4987G>C X 41064718 LUSC GT - Frameshift p.V1181Efs*12 c.3542_3543delTG X 41043909 UCEC G T Missense p.D1695Y c.5083G>T X 41069829 HNSC G T Missense p.D1761Y c.5281G>T X 41073912 BRCA G T Missense p.G1068V c.3203G>T X 41043305 CM G T Missense p.G139V c.416G>T X 40994071 LUSC G T Missense p.G1481V c.4442G>T X 41057842 LUAD G T Missense p.R1348L c.4043G>T X 41055569 LUAD G T Missense p.R1672M c.5015G>T X 41064746 LUAD G T Missense p.R83L c.248G>T X 40990715 HNSC G T Missense p.W1804C c.5412G>T X 41075232 CM G T Missense p.W2417C c.7251G>T X 41088852 LUAD G T Missense p.W512L c.1535G>T X 41007737 HNSC G T Nonsense p.E2038* c.6112G>T X 41076499 BRCA G T Nonsense p.E61* c.181G>T X 40988337 THCA - GT SpliceDonorInsertion . c.3810+1_3810+2insGT X 41047371 BLCA G T Synonymous p.T798T c.2394G>T X 41026800 UCEC GTTT - Frameshift p.F580Vfs*7 c.1738_1741delTTTG X 41010280 CM TA - Frameshift p.Y630Cfs*2 c.1889_1890delAT X 41012323 THCA T A SpliceDonorSNV . c.6565+2T>A X 41078486 LUSC T A Synonymous p.G189G c.567T>A X 40996188 UCEC T C Missense p.I1463T c.4388T>C X 41057788 LGG T C Missense p.I2120T c.6359T>C X 41077774 RCCC T C SpliceDonorSNV . c.1897+2T>C X 41012336 STAD T C Synonymous p.L1789L c.5365T>C X 41075185 BRCA T C Synonymous p.N1888N c.5664T>C X 41075484 CM - T Frameshift p.R1896Sfs*4 c.5685dupT X 41075505 LUSC - T Frameshift p.Y1939Lfs*16 c.5815dupT X 41075635 LUSC T G SpliceDonorSNV . c.4086+2T>G X 41055614 CM TTC - InFrameDeletion p.L1586delL c.4756_4758delCTT X 41060463 UCEC TTCT - IntronicDeletion . c.1-6050_1-6047delCTTT X 40976830 CLL