Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change BLCA 9 21333009 21333009 + Missense_Mutation SNP G G C TCGA-S5-A6DX-01A-11D-A31L-08 TCGA-S5-A6DX-10A-01D-A31J-08 g.chr9:21333009G>C c.1850C>G c.(1849-1851)tCt>tGt p.S617C BLCA 9 21333031 21333031 + Missense_Mutation SNP G G C TCGA-UY-A78L-01A-12D-A339-08 TCGA-UY-A78L-10A-01D-A339-08 g.chr9:21333031G>C c.1828C>G c.(1828-1830)Ctt>Gtt p.L610V BLCA 9 21333682 21333682 + Missense_Mutation SNP G G A TCGA-E7-A7XN-01A-11D-A34U-08 TCGA-E7-A7XN-10A-01D-A34X-08 g.chr9:21333682G>A c.1177C>T c.(1177-1179)Cac>Tac p.H393Y BLCA 9 21333785 21333785 + Silent SNP A A G TCGA-E7-A85H-01A-11D-A34U-08 TCGA-E7-A85H-10B-01D-A34X-08 g.chr9:21333785A>G c.1074T>C c.(1072-1074)taT>taC p.Y358Y BLCA 9 21334109 21334109 + Silent SNP G G A TCGA-E5-A4U1-01A-11D-A31L-08 TCGA-E5-A4U1-10B-01D-A31J-08 g.chr9:21334109G>A c.750C>T c.(748-750)ctC>ctT p.L250L BLCA 9 21334174 21334174 + Missense_Mutation SNP G G A TCGA-DK-A2I4-01A-11D-A21A-08 TCGA-DK-A2I4-10A-01D-A21A-08 g.chr9:21334174G>A c.685C>T c.(685-687)Cgg>Tgg p.R229W BLCA 9 21334288 21334288 + Silent SNP G G A TCGA-G2-AA3B-01A-11D-A391-08 TCGA-G2-AA3B-10A-01D-A394-08 g.chr9:21334288G>A c.571C>T c.(571-573)Cta>Tta p.L191L BLCA 9 21334469 21334469 + Silent SNP G G A TCGA-KQ-A41N-01A-11D-A339-08 TCGA-KQ-A41N-10D-01D-A339-08 g.chr9:21334469G>A c.390C>T c.(388-390)agC>agT p.S130S BLCA 9 21334596 21334596 + Missense_Mutation SNP T T C TCGA-DK-A1AD-01A-11D-A13W-08 TCGA-DK-A1AD-10A-01D-A13W-08 g.chr9:21334596T>C c.263A>G c.(262-264)cAa>cGa p.Q88R BLCA 9 21334735 21334735 + Nonsense_Mutation SNP G G A TCGA-UY-A9PF-01A-11D-A38G-08 TCGA-UY-A9PF-10A-01D-A38J-08 g.chr9:21334735G>A c.124C>T c.(124-126)Cag>Tag p.Q42* BLCA 9 21334821 21334821 + Missense_Mutation SNP G G A TCGA-XF-A9T3-01A-11D-A42E-08 TCGA-XF-A9T3-10A-01D-A42H-08 g.chr9:21334821G>A c.38C>T c.(37-39)tCt>tTt p.S13F BRCA 9 21333116 21333116 + Silent SNP T T A TCGA-LL-A50Y-01A-11D-A25Q-09 TCGA-LL-A50Y-10A-01D-A25Q-09 g.chr9:21333116T>A c.1743A>T c.(1741-1743)ccA>ccT p.P581P BRCA 9 21333117 21333117 + Frame_Shift_Del DEL G G - TCGA-OL-A5S0-01A-11D-A28B-09 TCGA-OL-A5S0-10A-01D-A28E-09 g.chr9:21333117delG c.1742delC c.(1741-1743)ccafs p.P581fs BRCA 9 21334138 21334138 + Nonsense_Mutation SNP G G A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr9:21334138G>A c.721C>T c.(721-723)Cga>Tga p.R241* BRCA 9 21334225 21334225 + Missense_Mutation SNP C C T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr9:21334225C>T c.634G>A c.(634-636)Gaa>Aaa p.E212K BRCA 9 21334269 21334269 + Missense_Mutation SNP C C T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr9:21334269C>T c.590G>A c.(589-591)cGa>cAa p.R197Q BRCA 9 21334379 21334379 + Silent SNP A A G TCGA-D8-A1XK-01A-21D-A14K-09 TCGA-D8-A1XK-10A-01D-A14K-09 g.chr9:21334379A>G c.480T>C c.(478-480)atT>atC p.I160I CESC 9 21334600 21334600 + Missense_Mutation SNP C C G TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chr9:21334600C>G c.259G>C c.(259-261)Gaa>Caa p.E87Q COAD 9 21333028 21333028 + Missense_Mutation SNP A A G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr9:21333028A>G c.1831T>C c.(1831-1833)Tca>Cca p.S611P COAD 9 21333218 21333218 + Silent SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr9:21333218G>A c.1641C>T c.(1639-1641)atC>atT p.I547I COAD 9 21333610 21333610 + Nonsense_Mutation SNP C C A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr9:21333610C>A c.1249G>T c.(1249-1251)Gaa>Taa p.E417* COAD 9 21333640 21333640 + Missense_Mutation SNP G G T TCGA-CK-4948-01B-11D-1650-10 TCGA-CK-4948-10A-01D-1650-10 g.chr9:21333640G>T c.1219C>A c.(1219-1221)Cgc>Agc p.R407S COAD 9 21333693 21333693 + Missense_Mutation SNP C C T TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr9:21333693C>T c.1166G>A c.(1165-1167)cGc>cAc p.R389H COAD 9 21333883 21333883 + Nonsense_Mutation SNP C C A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr9:21333883C>A c.976G>T c.(976-978)Gaa>Taa p.E326* COAD 9 21333995 21333995 + Silent SNP T T C TCGA-G4-6293-01A-11D-1719-10 TCGA-G4-6293-10A-01D-1719-10 g.chr9:21333995T>C c.864A>G c.(862-864)tcA>tcG p.S288S COAD 9 21334137 21334137 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr9:21334137C>T c.722G>A c.(721-723)cGa>cAa p.R241Q COAD 9 21334424 21334427 + Frame_Shift_Del DEL AAGA AAGA - TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr9:21334424_21334427delAAGA c.432_435delTCTT c.(430-435)tttcttfs p.FL144fs COAD 9 21334512 21334512 + Missense_Mutation SNP G G T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr9:21334512G>T c.347C>A c.(346-348)tCt>tAt p.S116Y COAD 9 21334628 21334628 + Missense_Mutation SNP G G C TCGA-DM-A285-01A-11D-A16V-10 TCGA-DM-A285-10A-01D-A16V-10 g.chr9:21334628G>C c.231C>G c.(229-231)ttC>ttG p.F77L COAD 9 21334756 21334756 + Missense_Mutation SNP C C T TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr9:21334756C>T c.103G>A c.(103-105)Gtg>Atg p.V35M COAD 9 21334808 21334808 + Silent SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr9:21334808C>T c.51G>A c.(49-51)caG>caA p.Q17Q COADREAD 9 21333028 21333028 + Missense_Mutation SNP A A G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr9:21333028A>G c.1831T>C c.(1831-1833)Tca>Cca p.S611P COADREAD 9 21333218 21333218 + Silent SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr9:21333218G>A c.1641C>T c.(1639-1641)atC>atT p.I547I COADREAD 9 21333610 21333610 + Nonsense_Mutation SNP C C A TCGA-AA-3977-01A-01W-0995-10 TCGA-AA-3977-10A-01W-0999-10 g.chr9:21333610C>A c.1249G>T c.(1249-1251)Gaa>Taa p.E417* COADREAD 9 21333625 21333625 + Nonsense_Mutation SNP C C A TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr9:21333625C>A c.1234G>T c.(1234-1236)Gaa>Taa p.E412* COADREAD 9 21333629 21333629 + Silent SNP A A G TCGA-F5-6813-01A-11D-1826-10 TCGA-F5-6813-10A-01D-1826-10 g.chr9:21333629A>G c.1230T>C c.(1228-1230)gcT>gcC p.A410A COADREAD 9 21333640 21333640 + Missense_Mutation SNP G G T TCGA-CK-4948-01B-11D-1650-10 TCGA-CK-4948-10A-01D-1650-10 g.chr9:21333640G>T c.1219C>A c.(1219-1221)Cgc>Agc p.R407S COADREAD 9 21333693 21333693 + Missense_Mutation SNP C C T TCGA-AA-3525-01A-02W-0833-10 TCGA-AA-3525-10A-01W-0833-10 g.chr9:21333693C>T c.1166G>A c.(1165-1167)cGc>cAc p.R389H COADREAD 9 21333736 21333736 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr9:21333736G>A c.1123C>T c.(1123-1125)Cgg>Tgg p.R375W COADREAD 9 21333883 21333883 + Nonsense_Mutation SNP C C A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr9:21333883C>A c.976G>T c.(976-978)Gaa>Taa p.E326* COADREAD 9 21333995 21333995 + Silent SNP T T C TCGA-G4-6293-01A-11D-1719-10 TCGA-G4-6293-10A-01D-1719-10 g.chr9:21333995T>C c.864A>G c.(862-864)tcA>tcG p.S288S COADREAD 9 21334137 21334137 + Missense_Mutation SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr9:21334137C>T c.722G>A c.(721-723)cGa>cAa p.R241Q COADREAD 9 21334424 21334427 + Frame_Shift_Del DEL AAGA AAGA - TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr9:21334424_21334427delAAGA c.432_435delTCTT c.(430-435)tttcttfs p.FL144fs COADREAD 9 21334512 21334512 + Missense_Mutation SNP G G T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr9:21334512G>T c.347C>A c.(346-348)tCt>tAt p.S116Y COADREAD 9 21334628 21334628 + Missense_Mutation SNP G G C TCGA-DM-A285-01A-11D-A16V-10 TCGA-DM-A285-10A-01D-A16V-10 g.chr9:21334628G>C c.231C>G c.(229-231)ttC>ttG p.F77L COADREAD 9 21334756 21334756 + Missense_Mutation SNP C C T TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr9:21334756C>T c.103G>A c.(103-105)Gtg>Atg p.V35M COADREAD 9 21334808 21334808 + Silent SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr9:21334808C>T c.51G>A c.(49-51)caG>caA p.Q17Q ESCA 9 21333629 21333629 + Silent SNP A A G TCGA-VR-A8EO-01A-11D-A36J-09 TCGA-VR-A8EO-10A-01D-A36M-09 g.chr9:21333629A>G c.1230T>C c.(1228-1230)gcT>gcC p.A410A GBMLGG 9 21333832 21333832 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:21333832C>A c.1027G>T c.(1027-1029)Gct>Tct p.A343S GBMLGG 9 21333865 21333865 + Missense_Mutation SNP G G A TCGA-E1-5318-01A-01D-1468-08 TCGA-E1-5318-10A-01D-1468-08 g.chr9:21333865G>A c.994C>T c.(994-996)Cca>Tca p.P332S GBMLGG 9 21334319 21334319 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:21334319G>A c.540C>T c.(538-540)aaC>aaT p.N180N HNSC 9 21333198 21333198 + Missense_Mutation SNP G G A TCGA-CN-5369-01A-01D-1434-08 TCGA-CN-5369-10A-01D-1434-08 g.chr9:21333198G>A c.1661C>T c.(1660-1662)tCt>tTt p.S554F HNSC 9 21333736 21333736 + Missense_Mutation SNP G G A TCGA-CV-7422-01A-21D-2078-08 TCGA-CV-7422-10A-01D-2078-08 g.chr9:21333736G>A c.1123C>T c.(1123-1125)Cgg>Tgg p.R375W HNSC 9 21334148 21334148 + Missense_Mutation SNP C C T TCGA-HD-A6HZ-01A-12D-A31L-08 TCGA-HD-A6HZ-10A-01D-A31J-08 g.chr9:21334148C>T c.711G>A c.(709-711)atG>atA p.M237I KIPAN 9 21334022 21334022 + Missense_Mutation SNP C C T TCGA-B8-5550-01A-01D-1534-10 TCGA-B8-5550-10A-01D-1535-10 g.chr9:21334022C>T c.837G>A c.(835-837)atG>atA p.M279I KIPAN 9 21334413 21334413 + Missense_Mutation SNP A A T TCGA-AL-3472-01A-01D-1252-08 TCGA-AL-3472-10A-01D-1252-08 g.chr9:21334413A>T c.446T>A c.(445-447)gTc>gAc p.V149D KIRC 9 21334022 21334022 + Missense_Mutation SNP C C T TCGA-B8-5550-01A-01D-1534-10 TCGA-B8-5550-10A-01D-1535-10 g.chr9:21334022C>T c.837G>A c.(835-837)atG>atA p.M279I KIRP 9 21334413 21334413 + Missense_Mutation SNP A A T TCGA-AL-3472-01A-01D-1252-08 TCGA-AL-3472-10A-01D-1252-08 g.chr9:21334413A>T c.446T>A c.(445-447)gTc>gAc p.V149D LGG 9 21333832 21333832 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:21333832C>A c.1027G>T c.(1027-1029)Gct>Tct p.A343S LGG 9 21333865 21333865 + Missense_Mutation SNP G G A TCGA-E1-5318-01A-01D-1468-08 TCGA-E1-5318-10A-01D-1468-08 g.chr9:21333865G>A c.994C>T c.(994-996)Cca>Tca p.P332S LGG 9 21334319 21334319 + Silent SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:21334319G>A c.540C>T c.(538-540)aaC>aaT p.N180N LIHC 9 21334288 21334288 + Silent SNP G G A TCGA-DD-A11A-01A-11D-A12Z-10 TCGA-DD-A11A-10A-01D-A12Z-10 g.chr9:21334288G>A c.571C>T c.(571-573)Cta>Tta p.L191L LIHC 9 21334479 21334479 + Missense_Mutation SNP T T C TCGA-G3-A6UC-01A-21D-A33K-10 TCGA-G3-A6UC-10A-01D-A33K-10 g.chr9:21334479T>C c.380A>G c.(379-381)gAa>gGa p.E127G LIHC 9 21334572 21334572 + Missense_Mutation SNP T T G TCGA-DD-A4NS-01A-11D-A30V-10 TCGA-DD-A4NS-10A-01D-A30V-10 g.chr9:21334572T>G c.287A>C c.(286-288)cAt>cCt p.H96P LUAD 9 21333334 21333334 + Missense_Mutation SNP A A G TCGA-50-5931-01A-11D-1753-08 TCGA-50-5931-11A-01D-1753-08 g.chr9:21333334A>G c.1525T>C c.(1525-1527)Tat>Cat p.Y509H LUAD 9 21333798 21333798 + Missense_Mutation SNP C C G TCGA-38-4630-01A-01D-1265-08 TCGA-38-4630-11A-01D-1265-08 g.chr9:21333798C>G c.1061G>C c.(1060-1062)gGt>gCt p.G354A LUAD 9 21334009 21334009 + Missense_Mutation SNP G G C TCGA-55-7914-01A-11D-2167-08 TCGA-55-7914-10A-01D-2167-08 g.chr9:21334009G>C c.850C>G c.(850-852)Cca>Gca p.P284A LUAD 9 21334168 21334168 + Missense_Mutation SNP C C A TCGA-64-5778-01A-01D-1625-08 TCGA-64-5778-10A-01D-1625-08 g.chr9:21334168C>A c.691G>T c.(691-693)Gat>Tat p.D231Y LUAD 9 21334680 21334680 + Missense_Mutation SNP T T C TCGA-17-Z025-01A-01W-0746-08 TCGA-17-Z025-11A-01W-0746-08 g.chr9:21334680T>C c.179A>G c.(178-180)gAt>gGt p.D60G LUAD 9 21334683 21334683 + Missense_Mutation SNP C C T TCGA-93-8067-01A-11D-2284-08 TCGA-93-8067-10A-01D-2284-08 g.chr9:21334683C>T c.176G>A c.(175-177)gGa>gAa p.G59E LUAD 9 21334730 21334730 + Silent SNP A A G TCGA-71-6725-01A-11D-1855-08 TCGA-71-6725-10A-01D-1855-08 g.chr9:21334730A>G c.129T>C c.(127-129)ctT>ctC p.L43L LUAD 9 21334826 21334826 + Silent SNP G G A TCGA-75-5126-01A-01D-1753-08 TCGA-75-5126-10A-01D-1753-08 g.chr9:21334826G>A c.33C>T c.(31-33)ggC>ggT p.G11G LUSC 9 21333175 21333175 + Missense_Mutation SNP C C G TCGA-66-2763-01A-01D-1522-08 TCGA-66-2763-11A-01D-1522-08 g.chr9:21333175C>G c.1684G>C c.(1684-1686)Gaa>Caa p.E562Q LUSC 9 21333559 21333559 + Missense_Mutation SNP C C T TCGA-34-5236-01A-21D-1817-08 TCGA-34-5236-10A-01D-1817-08 g.chr9:21333559C>T c.1300G>A c.(1300-1302)Gaa>Aaa p.E434K LUSC 9 21333639 21333639 + Missense_Mutation SNP C C A TCGA-22-1016-01A-01D-1521-08 TCGA-22-1016-11A-01D-1521-08 g.chr9:21333639C>A c.1220G>T c.(1219-1221)cGc>cTc p.R407L LUSC 9 21333994 21333994 + Missense_Mutation SNP C C T TCGA-18-3414-01A-01D-0983-08 TCGA-18-3414-11A-01D-0983-08 g.chr9:21333994C>T c.865G>A c.(865-867)Gat>Aat p.D289N LUSC 9 21334855 21334855 + Missense_Mutation SNP T T C TCGA-66-2770-01A-01D-1522-08 TCGA-66-2770-11A-01D-1522-08 g.chr9:21334855T>C c.4A>G c.(4-6)Aaa>Gaa p.K2E OV 9 21333117 21333117 + Missense_Mutation SNP G G A TCGA-24-1418-01A-01W-0549-09 TCGA-24-1418-10A-01W-0549-09 g.chr9:21333117G>A c.1742C>T c.(1741-1743)cCa>cTa p.P581L OV 9 21333629 21333629 + Silent SNP A A G TCGA-59-2352-01A-01W-0799-08 TCGA-59-2352-10A-01W-0800-08 g.chr9:21333629A>G c.1230T>C c.(1228-1230)gcT>gcC p.A410A OV 9 21333640 21333640 + Missense_Mutation SNP G G A TCGA-57-1582-01A-01W-0615-10 TCGA-57-1582-11A-01W-0615-10 g.chr9:21333640G>A c.1219C>T c.(1219-1221)Cgc>Tgc p.R407C OV 9 21333996 21333996 + Nonsense_Mutation SNP G G C TCGA-23-2078-01A-01W-0722-08 TCGA-23-2078-10A-01W-0722-08 g.chr9:21333996G>C c.863C>G c.(862-864)tCa>tGa p.S288* PAAD 9 21333707 21333707 + Silent SNP T T G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:21333707T>G c.1152A>C c.(1150-1152)tcA>tcC p.S384S PAAD 9 21334090 21334090 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:21334090C>T c.769G>A c.(769-771)Gta>Ata p.V257I PRAD 9 21333237 21333237 + Missense_Mutation SNP G G A TCGA-EJ-5532-01A-01D-1576-08 TCGA-EJ-5532-10A-01D-1577-08 g.chr9:21333237G>A c.1622C>T c.(1621-1623)gCc>gTc p.A541V PRAD 9 21334407 21334408 + Frame_Shift_Del DEL AA AA - TCGA-J4-A67Q-01A-21D-A30E-08 TCGA-J4-A67Q-10A-01D-A30H-08 g.chr9:21334407_21334408delAA c.451_452delTT c.(451-453)ttgfs p.L151fs PRAD 9 21334742 21334742 + Silent SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr9:21334742G>A c.117C>T c.(115-117)ggC>ggT p.G39G READ 9 21333625 21333625 + Nonsense_Mutation SNP C C A TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr9:21333625C>A c.1234G>T c.(1234-1236)Gaa>Taa p.E412* READ 9 21333629 21333629 + Silent SNP A A G TCGA-F5-6813-01A-11D-1826-10 TCGA-F5-6813-10A-01D-1826-10 g.chr9:21333629A>G c.1230T>C c.(1228-1230)gcT>gcC p.A410A READ 9 21333736 21333736 + Missense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr9:21333736G>A c.1123C>T c.(1123-1125)Cgg>Tgg p.R375W SKCM 9 21333565 21333565 + Frame_Shift_Del DEL T T - TCGA-D3-A51R-06A-11D-A25O-08 TCGA-D3-A51R-10A-01D-A25O-08 g.chr9:21333565delT c.1294delA c.(1294-1296)atgfs p.M432fs SKCM 9 21334327 21334327 + Silent SNP G G A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr9:21334327G>A c.532C>T c.(532-534)Ctg>Ttg p.L178L SKCM 9 21334623 21334623 + Missense_Mutation SNP G G A TCGA-D3-A5GU-06A-11D-A27K-08 TCGA-D3-A5GU-10A-01D-A27N-08 g.chr9:21334623G>A c.236C>T c.(235-237)gCc>gTc p.A79V

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 9 21334678 21334678 single base substitution C T intron_variant BLCA-CN 9 21334678 21334678 single base substitution C T missense_variant E61K 181G>A BLCA-US 9 21334174 21334174 single base substitution G A missense_variant R161W 481C>T BLCA-US 9 21334174 21334174 single base substitution G A missense_variant R229W 685C>T BLCA-US 9 21334596 21334596 single base substitution T C missense_variant Q20R 59A>G BLCA-US 9 21334596 21334596 single base substitution T C missense_variant Q88R 263A>G BOCA-FR 9 21326313 21326313 single base substitution A G downstream_gene_variant BRCA-EU 9 21328156 21328159 deletion of <=200bp TTGA - downstream_gene_variant BRCA-EU 9 21328567 21328568 deletion of <=200bp CA - downstream_gene_variant BRCA-EU 9 21328678 21328678 deletion of <=200bp A - downstream_gene_variant BRCA-EU 9 21330176 21330176 single base substitution C A 3_prime_UTR_variant BRCA-EU 9 21330176 21330176 single base substitution C A downstream_gene_variant BRCA-EU 9 21330219 21330219 single base substitution C T 3_prime_UTR_variant BRCA-EU 9 21330219 21330219 single base substitution C T downstream_gene_variant BRCA-EU 9 21331331 21331331 single base substitution C T 3_prime_UTR_variant BRCA-EU 9 21331331 21331331 single base substitution C T downstream_gene_variant BRCA-EU 9 21331891 21331891 single base substitution G A 3_prime_UTR_variant BRCA-EU 9 21334148 21334148 single base substitution C T missense_variant M169I 507G>A BRCA-EU 9 21334148 21334148 single base substitution C T missense_variant M237I 711G>A BRCA-EU 9 21334683 21334683 single base substitution C T intron_variant BRCA-EU 9 21334683 21334683 single base substitution C T missense_variant G59E 176G>A BRCA-EU 9 21335193 21335193 single base substitution T C 5_prime_UTR_variant BRCA-EU 9 21335494 21335494 single base substitution G T upstream_gene_variant BRCA-EU 9 21336457 21336457 deletion of <=200bp T - upstream_gene_variant BRCA-EU 9 21336457 21336457 insertion of <=200bp - T upstream_gene_variant BRCA-EU 9 21336866 21336866 single base substitution T C upstream_gene_variant BRCA-EU 9 21336937 21336937 deletion of <=200bp T - upstream_gene_variant BRCA-EU 9 21338349 21338349 single base substitution C G upstream_gene_variant BRCA-EU 9 21340251 21340251 single base substitution G A upstream_gene_variant BRCA-FR 9 21335193 21335193 single base substitution T C 5_prime_UTR_variant BRCA-US 9 21333116 21333116 single base substitution T A synonymous_variant P513P 1539A>T BRCA-US 9 21333116 21333116 single base substitution T A synonymous_variant P581P 1743A>T BRCA-US 9 21333117 21333117 deletion of <=200bp G - frameshift_variant P513 BRCA-US 9 21333117 21333117 deletion of <=200bp G - frameshift_variant P581 BRCA-US 9 21334138 21334138 single base substitution G A stop_gained R173* 517C>T BRCA-US 9 21334138 21334138 single base substitution G A stop_gained R241* 721C>T BRCA-US 9 21334225 21334225 single base substitution C T missense_variant E144K 430G>A BRCA-US 9 21334225 21334225 single base substitution C T missense_variant E212K 634G>A BRCA-US 9 21334269 21334269 single base substitution C T missense_variant R129Q 386G>A BRCA-US 9 21334269 21334269 single base substitution C T missense_variant R197Q 590G>A BRCA-US 9 21334379 21334379 single base substitution A G synonymous_variant I160I 480T>C BRCA-US 9 21334379 21334379 single base substitution A G synonymous_variant I92I 276T>C CESC-US 9 21334600 21334600 single base substitution C G missense_variant E19Q 55G>C CESC-US 9 21334600 21334600 single base substitution C G missense_variant E87Q 259G>C COAD-US 9 21333097 21333097 single base substitution G A stop_gained R520* 1558C>T COAD-US 9 21333097 21333097 single base substitution G A stop_gained R588* 1762C>T COAD-US 9 21333883 21333883 single base substitution C A stop_gained E258* 772G>T COAD-US 9 21333883 21333883 single base substitution C A stop_gained E326* 976G>T COAD-US 9 21334424 21334427 deletion of <=200bp AAGA - frameshift_variant FL144 COAD-US 9 21334424 21334427 deletion of <=200bp AAGA - frameshift_variant FL76 COAD-US 9 21334512 21334512 insertion of <=200bp - A frameshift_variant S116S? COAD-US 9 21334512 21334512 insertion of <=200bp - A frameshift_variant S48S? COAD-US 9 21334628 21334628 single base substitution G C missense_variant F77L 231C>G COAD-US 9 21334628 21334628 single base substitution G C missense_variant F9L 27C>G COAD-US 9 21334756 21334756 single base substitution C T intron_variant COAD-US 9 21334756 21334756 single base substitution C T missense_variant V35M 103G>A COAD-US 9 21334808 21334808 single base substitution C T intron_variant COAD-US 9 21334808 21334808 single base substitution C T synonymous_variant Q17Q 51G>A COCA-CN 9 21325193 21325193 single base substitution T C downstream_gene_variant COCA-CN 9 21329223 21329223 single base substitution C T downstream_gene_variant COCA-CN 9 21332059 21332059 single base substitution T G 3_prime_UTR_variant COCA-CN 9 21333619 21333619 single base substitution C T missense_variant A346T 1036G>A COCA-CN 9 21333619 21333619 single base substitution C T missense_variant A414T 1240G>A COCA-CN 9 21334322 21334322 single base substitution C A missense_variant K111N 333G>T COCA-CN 9 21334322 21334322 single base substitution C A missense_variant K179N 537G>T COCA-CN 9 21334547 21334547 single base substitution C A missense_variant K104N 312G>T COCA-CN 9 21334547 21334547 single base substitution C A missense_variant K36N 108G>T COCA-CN 9 21334679 21334679 single base substitution A G intron_variant COCA-CN 9 21334679 21334679 single base substitution A G synonymous_variant D60D 180T>C COCA-CN 9 21337454 21337454 single base substitution G A upstream_gene_variant EOPC-DE 9 21332911 21332911 single base substitution A G 3_prime_UTR_variant ESAD-UK 9 21327917 21327917 deletion of <=200bp T - downstream_gene_variant ESAD-UK 9 21331508 21331508 insertion of <=200bp - AC 3_prime_UTR_variant ESAD-UK 9 21331508 21331508 insertion of <=200bp - AC downstream_gene_variant ESAD-UK 9 21333925 21333925 single base substitution C T missense_variant V244I 730G>A ESAD-UK 9 21333925 21333925 single base substitution C T missense_variant V312I 934G>A ESAD-UK 9 21337381 21337381 single base substitution C T upstream_gene_variant ESAD-UK 9 21337675 21337675 single base substitution C A upstream_gene_variant ESAD-UK 9 21338408 21338408 single base substitution A C upstream_gene_variant ESAD-UK 9 21340192 21340192 single base substitution T G upstream_gene_variant KIRC-US 9 21334022 21334022 single base substitution C T missense_variant M211I 633G>A KIRC-US 9 21334022 21334022 single base substitution C T missense_variant M279I 837G>A KIRP-US 9 21334413 21334413 single base substitution A T missense_variant V149D 446T>A KIRP-US 9 21334413 21334413 single base substitution A T missense_variant V81D 242T>A LGG-US 9 21333865 21333865 single base substitution G A missense_variant P264S 790C>T LGG-US 9 21333865 21333865 single base substitution G A missense_variant P332S 994C>T LIHC-US 9 21334288 21334288 single base substitution G A synonymous_variant L123L 367C>T LIHC-US 9 21334288 21334288 single base substitution G A synonymous_variant L191L 571C>T LIHC-US 9 21334479 21334479 single base substitution T C missense_variant E127G 380A>G LIHC-US 9 21334479 21334479 single base substitution T C missense_variant E59G 176A>G LIHC-US 9 21334572 21334572 single base substitution T G missense_variant H28P 83A>C LIHC-US 9 21334572 21334572 single base substitution T G missense_variant H96P 287A>C LIRI-JP 9 21327362 21327364 deletion of <=200bp CAT - downstream_gene_variant LIRI-JP 9 21328141 21328141 single base substitution A T downstream_gene_variant LIRI-JP 9 21328282 21328282 single base substitution T C downstream_gene_variant LIRI-JP 9 21329390 21329390 single base substitution T C downstream_gene_variant LIRI-JP 9 21329864 21329864 single base substitution G A 3_prime_UTR_variant LIRI-JP 9 21329864 21329864 single base substitution G A downstream_gene_variant LIRI-JP 9 21329893 21329893 single base substitution T C 3_prime_UTR_variant LIRI-JP 9 21329893 21329893 single base substitution T C downstream_gene_variant LIRI-JP 9 21331112 21331112 single base substitution G C 3_prime_UTR_variant LIRI-JP 9 21331112 21331112 single base substitution G C downstream_gene_variant LIRI-JP 9 21334132 21334132 single base substitution G A missense_variant P175S 523C>T LIRI-JP 9 21334132 21334132 single base substitution G A missense_variant P243S 727C>T LIRI-JP 9 21334776 21334776 single base substitution G A intron_variant LIRI-JP 9 21334776 21334776 single base substitution G A missense_variant T28I 83C>T LIRI-JP 9 21334892 21334892 single base substitution C T 5_prime_UTR_variant LIRI-JP 9 21334892 21334892 single base substitution C T intron_variant LIRI-JP 9 21337057 21337057 single base substitution A G upstream_gene_variant LIRI-JP 9 21337214 21337214 single base substitution A G upstream_gene_variant LIRI-JP 9 21337438 21337438 single base substitution C T upstream_gene_variant LIRI-JP 9 21338421 21338421 single base substitution A T upstream_gene_variant LIRI-JP 9 21339064 21339064 single base substitution A T upstream_gene_variant LIRI-JP 9 21339777 21339777 single base substitution A T upstream_gene_variant LIRI-JP 9 21340100 21340100 single base substitution T C upstream_gene_variant LUSC-KR 9 21339931 21339931 single base substitution G T upstream_gene_variant LUSC-US 9 21333175 21333175 single base substitution C G missense_variant E494Q 1480G>C LUSC-US 9 21333175 21333175 single base substitution C G missense_variant E562Q 1684G>C LUSC-US 9 21333559 21333559 single base substitution C T missense_variant E366K 1096G>A LUSC-US 9 21333559 21333559 single base substitution C T missense_variant E434K 1300G>A LUSC-US 9 21333639 21333639 single base substitution C A missense_variant R339L 1016G>T LUSC-US 9 21333639 21333639 single base substitution C A missense_variant R407L 1220G>T LUSC-US 9 21333994 21333994 single base substitution C T missense_variant D221N 661G>A LUSC-US 9 21333994 21333994 single base substitution C T missense_variant D289N 865G>A LUSC-US 9 21334855 21334855 single base substitution T C intron_variant LUSC-US 9 21334855 21334855 single base substitution T C missense_variant K2E 4A>G MALY-DE 9 21325426 21325426 single base substitution T C downstream_gene_variant MALY-DE 9 21329764 21329765 deletion of <=200bp TA - 3_prime_UTR_variant MALY-DE 9 21329764 21329765 deletion of <=200bp TA - downstream_gene_variant MALY-DE 9 21337138 21337138 single base substitution A C upstream_gene_variant MELA-AU 9 21325837 21325837 single base substitution G A downstream_gene_variant MELA-AU 9 21325890 21325890 single base substitution G A downstream_gene_variant MELA-AU 9 21326220 21326220 single base substitution A G downstream_gene_variant MELA-AU 9 21327623 21327623 single base substitution G A downstream_gene_variant MELA-AU 9 21327974 21327974 single base substitution G A downstream_gene_variant MELA-AU 9 21330214 21330214 single base substitution A G 3_prime_UTR_variant MELA-AU 9 21330214 21330214 single base substitution A G downstream_gene_variant MELA-AU 9 21331494 21331494 single base substitution T G 3_prime_UTR_variant MELA-AU 9 21331494 21331494 single base substitution T G downstream_gene_variant MELA-AU 9 21333697 21333697 single base substitution T C missense_variant K320E 958A>G MELA-AU 9 21333697 21333697 single base substitution T C missense_variant K388E 1162A>G MELA-AU 9 21334338 21334338 single base substitution T C missense_variant N106S 317A>G MELA-AU 9 21334338 21334338 single base substitution T C missense_variant N174S 521A>G MELA-AU 9 21335052 21335052 single base substitution G A 5_prime_UTR_variant MELA-AU 9 21335052 21335052 single base substitution G A intron_variant MELA-AU 9 21335813 21335813 single base substitution C T upstream_gene_variant MELA-AU 9 21336314 21336314 single base substitution C T upstream_gene_variant MELA-AU 9 21336643 21336643 single base substitution C T upstream_gene_variant MELA-AU 9 21337343 21337343 single base substitution G A upstream_gene_variant MELA-AU 9 21337997 21337997 single base substitution A G upstream_gene_variant MELA-AU 9 21338154 21338154 single base substitution T G upstream_gene_variant MELA-AU 9 21338336 21338336 single base substitution G A upstream_gene_variant MELA-AU 9 21338352 21338353 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 9 21338442 21338442 single base substitution G A upstream_gene_variant MELA-AU 9 21338550 21338550 single base substitution C T upstream_gene_variant MELA-AU 9 21338845 21338845 single base substitution C T upstream_gene_variant MELA-AU 9 21338924 21338924 single base substitution A C upstream_gene_variant MELA-AU 9 21339010 21339010 single base substitution C T upstream_gene_variant MELA-AU 9 21339193 21339193 single base substitution C T upstream_gene_variant MELA-AU 9 21339374 21339374 single base substitution C T upstream_gene_variant MELA-AU 9 21339710 21339710 single base substitution G A upstream_gene_variant MELA-AU 9 21339824 21339824 single base substitution G A upstream_gene_variant MELA-AU 9 21339832 21339832 single base substitution G A upstream_gene_variant OV-AU 9 21325093 21325093 single base substitution C T downstream_gene_variant OV-AU 9 21325784 21325784 single base substitution C T downstream_gene_variant OV-AU 9 21331494 21331494 single base substitution T G 3_prime_UTR_variant OV-AU 9 21331494 21331494 single base substitution T G downstream_gene_variant OV-AU 9 21340193 21340193 single base substitution T A upstream_gene_variant OV-US 9 21333117 21333117 single base substitution G A missense_variant P513L 1538C>T OV-US 9 21333117 21333117 single base substitution G A missense_variant P581L 1742C>T PACA-AU 9 21325112 21325112 single base substitution G A downstream_gene_variant PACA-AU 9 21326579 21326579 single base substitution T C downstream_gene_variant PACA-AU 9 21330737 21330737 single base substitution T A 3_prime_UTR_variant PACA-AU 9 21330737 21330737 single base substitution T A downstream_gene_variant PACA-AU 9 21332640 21332640 insertion of <=200bp - T 3_prime_UTR_variant PACA-CA 9 21325111 21325111 single base substitution G A downstream_gene_variant PACA-CA 9 21327515 21327515 single base substitution G A downstream_gene_variant PACA-CA 9 21328465 21328465 single base substitution C A downstream_gene_variant PACA-CA 9 21334492 21334492 single base substitution G A stop_gained Q123* 367C>T PACA-CA 9 21334492 21334492 single base substitution G A stop_gained Q55* 163C>T PACA-CA 9 21334571 21334571 single base substitution A C missense_variant H28Q 84T>G PACA-CA 9 21334571 21334571 single base substitution A C missense_variant H96Q 288T>G PACA-CA 9 21334581 21334581 single base substitution A C missense_variant I25S 74T>G PACA-CA 9 21334581 21334581 single base substitution A C missense_variant I93S 278T>G PAEN-IT 9 21338160 21338160 single base substitution G A upstream_gene_variant PAEN-IT 9 21339959 21339959 single base substitution C A upstream_gene_variant PBCA-DE 9 21327812 21327813 deletion of <=200bp AC - downstream_gene_variant PBCA-DE 9 21329388 21329388 single base substitution A T downstream_gene_variant PBCA-DE 9 21329764 21329765 deletion of <=200bp TA - 3_prime_UTR_variant PBCA-DE 9 21329764 21329765 deletion of <=200bp TA - downstream_gene_variant PBCA-DE 9 21335779 21335779 insertion of <=200bp - T upstream_gene_variant PRAD-UK 9 21332013 21332013 single base substitution T C 3_prime_UTR_variant PRAD-UK 9 21335177 21335177 single base substitution A C 5_prime_UTR_variant PRAD-US 9 21334407 21334408 deletion of <=200bp AA - frameshift_variant L151 PRAD-US 9 21334407 21334408 deletion of <=200bp AA - frameshift_variant L83 RECA-EU 9 21338355 21338355 single base substitution G A upstream_gene_variant SKCA-BR 9 21325754 21325754 single base substitution G A downstream_gene_variant SKCA-BR 9 21329347 21329347 single base substitution G A downstream_gene_variant SKCA-BR 9 21330187 21330187 single base substitution G A 3_prime_UTR_variant SKCA-BR 9 21330187 21330187 single base substitution G A downstream_gene_variant SKCA-BR 9 21330726 21330726 single base substitution C A 3_prime_UTR_variant SKCA-BR 9 21330726 21330726 single base substitution C A downstream_gene_variant SKCA-BR 9 21330875 21330875 single base substitution T C 3_prime_UTR_variant SKCA-BR 9 21330875 21330875 single base substitution T C downstream_gene_variant SKCA-BR 9 21332797 21332797 insertion of <=200bp - CT 3_prime_UTR_variant SKCA-BR 9 21336859 21336859 single base substitution G A upstream_gene_variant SKCA-BR 9 21337560 21337560 single base substitution C T upstream_gene_variant SKCM-US 9 21333565 21333565 deletion of <=200bp T - frameshift_variant M364 SKCM-US 9 21333565 21333565 deletion of <=200bp T - frameshift_variant M432 SKCM-US 9 21334327 21334327 single base substitution G A synonymous_variant L110L 328C>T SKCM-US 9 21334327 21334327 single base substitution G A synonymous_variant L178L 532C>T SKCM-US 9 21334623 21334623 single base substitution G A missense_variant A11V 32C>T SKCM-US 9 21334623 21334623 single base substitution G A missense_variant A79V 236C>T STAD-US 9 21333123 21333123 single base substitution T A missense_variant D511V 1532A>T STAD-US 9 21333123 21333123 single base substitution T A missense_variant D579V 1736A>T STAD-US 9 21333437 21333437 single base substitution C T missense_variant M406I 1218G>A STAD-US 9 21333437 21333437 single base substitution C T missense_variant M474I 1422G>A STAD-US 9 21333640 21333640 single base substitution G A missense_variant R339C 1015C>T STAD-US 9 21333640 21333640 single base substitution G A missense_variant R407C 1219C>T STAD-US 9 21333694 21333694 single base substitution G A missense_variant R321C 961C>T STAD-US 9 21333694 21333694 single base substitution G A missense_variant R389C 1165C>T STAD-US 9 21333734 21333734 single base substitution C T synonymous_variant R307R 921G>A STAD-US 9 21333734 21333734 single base substitution C T synonymous_variant R375R 1125G>A STAD-US 9 21333894 21333894 single base substitution T C missense_variant E254G 761A>G STAD-US 9 21333894 21333894 single base substitution T C missense_variant E322G 965A>G STAD-US 9 21334270 21334270 single base substitution G A stop_gained R129* 385C>T STAD-US 9 21334270 21334270 single base substitution G A stop_gained R197* 589C>T STAD-US 9 21334480 21334480 single base substitution C T missense_variant E127K 379G>A STAD-US 9 21334480 21334480 single base substitution C T missense_variant E59K 175G>A STAD-US 9 21334793 21334793 single base substitution T C intron_variant STAD-US 9 21334793 21334793 single base substitution T C synonymous_variant G22G 66A>G THCA-SA 9 21332577 21332577 single base substitution A C 3_prime_UTR_variant THCA-SA 9 21332601 21332601 single base substitution C T 3_prime_UTR_variant THCA-SA 9 21332635 21332635 single base substitution C G 3_prime_UTR_variant THCA-SA 9 21333254 21333254 single base substitution T C synonymous_variant Q467Q 1401A>G THCA-SA 9 21333254 21333254 single base substitution T C synonymous_variant Q535Q 1605A>G THCA-SA 9 21334998 21334998 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant THCA-SA 9 21334998 21334998 single base substitution G A intron_variant THCA-SA 9 21335200 21335200 single base substitution C A 5_prime_UTR_variant THCA-SA 9 21335404 21335404 single base substitution A C upstream_gene_variant UCEC-US 9 21333154 21333154 single base substitution G T missense_variant P501T 1501C>A UCEC-US 9 21333154 21333154 single base substitution G T missense_variant P569T 1705C>A UCEC-US 9 21333273 21333273 single base substitution G A missense_variant A461V 1382C>T UCEC-US 9 21333273 21333273 single base substitution G A missense_variant A529V 1586C>T UCEC-US 9 21333395 21333395 single base substitution C T missense_variant M420I 1260G>A UCEC-US 9 21333395 21333395 single base substitution C T missense_variant M488I 1464G>A UCEC-US 9 21333570 21333570 single base substitution G A missense_variant A362V 1085C>T UCEC-US 9 21333570 21333570 single base substitution G A missense_variant A430V 1289C>T UCEC-US 9 21333734 21333734 single base substitution C T synonymous_variant R307R 921G>A UCEC-US 9 21333734 21333734 single base substitution C T synonymous_variant R375R 1125G>A UCEC-US 9 21333755 21333755 single base substitution T A synonymous_variant T300T 900A>T UCEC-US 9 21333755 21333755 single base substitution T A synonymous_variant T368T 1104A>T UCEC-US 9 21334100 21334100 single base substitution G A synonymous_variant Y185Y 555C>T UCEC-US 9 21334100 21334100 single base substitution G A synonymous_variant Y253Y 759C>T UCEC-US 9 21334545 21334545 single base substitution T G missense_variant K105T 314A>C UCEC-US 9 21334545 21334545 single base substitution T G missense_variant K37T 110A>C UCEC-US 9 21334591 21334591 single base substitution A G synonymous_variant L22L 64T>C UCEC-US 9 21334591 21334591 single base substitution A G synonymous_variant L90L 268T>C UCEC-US 9 21334600 21334600 single base substitution C A stop_gained E19* 55G>T UCEC-US 9 21334600 21334600 single base substitution C A stop_gained E87* 259G>T UCEC-US 9 21334621 21334621 single base substitution T C missense_variant M12V 34A>G UCEC-US 9 21334621 21334621 single base substitution T C missense_variant M80V 238A>G UCEC-US 9 21334720 21334720 single base substitution C A intron_variant UCEC-US 9 21334720 21334720 single base substitution C A stop_gained G47* 139G>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-18-3414-01 COSM753766 c.865G>A p.D289N Substitution - Missense 9:21333995-21333995 - PCSI_0083_Pa_P COSM3382497 c.278T>G p.I93S Substitution - Missense 9:21334582-21334582 - TCGA-AL-3472-01 COSM3996492 c.446T>A p.V149D Substitution - Missense 9:21334414-21334414 - PCSI_0083_Pa_X COSM3382495 c.367C>T p.Q123* Substitution - Nonsense 9:21334493-21334493 - YUKAT COSM5410922 c.1196G>A p.G399E Substitution - Missense 9:21333664-21333664 - PCSI_0083_Pa_X COSM3382497 c.278T>G p.I93S Substitution - Missense 9:21334582-21334582 - TCGA-AM-5820-01 COSM3092044 c.1762C>T p.R588* Substitution - Nonsense 9:21333098-21333098 - LUAD-D01603 COSM338105 c.787G>C p.D263H Substitution - Missense 9:21334073-21334073 - TCGA-OL-A5S0-01 COSM5835717 c.1742delC p.P581fs*>37 Deletion - Frameshift 9:21333118-21333118 - TCGA-66-2770-01 COSM753765 c.4A>G p.K2E Substitution - Missense 9:21334856-21334856 - LUAD-CHTN-MAD06-00668 COSM360495 c.1273G>T p.E425* Substitution - Nonsense 9:21333587-21333587 - TCGA-E1-5318-01 COSM3930000 c.994C>T p.P332S Substitution - Missense 9:21333866-21333866 - ME045T COSM229523 c.668T>C p.L223P Substitution - Missense 9:21334192-21334192 - TCGA-B5-A0K2-01 COSM1107840 c.1079C>A p.T360K Substitution - Missense 9:21333781-21333781 - TCGA-AX-A05Z-01 COSM1107845 c.259G>T p.E87* Substitution - Nonsense 9:21334601-21334601 - TCGA-B5-A0JY-01 COSM1107841 c.759C>T p.Y253Y Substitution - coding silent 9:21334101-21334101 - TCGA-DK-A1AD-01 COSM1314723 c.263A>G p.Q88R Substitution - Missense 9:21334597-21334597 - TCGA-B5-A11E-01 COSM1107844 c.268T>C p.L90L Substitution - coding silent 9:21334592-21334592 - TCGA-G3-A6UC-01 COSM4929794 c.380A>G p.E127G Substitution - Missense 9:21334480-21334480 - TCGA-G4-6628-01 COSM1461776 c.103G>A p.V35M Substitution - Missense 9:21334757-21334757 - TCGA-AA-A010-01 COSM282290 c.347C>A p.S116Y Substitution - Missense 9:21334513-21334513 - TCGA-G4-6298-01 COSM5174132 c.346_347insT p.S116fs*3 Insertion - Frameshift 9:21334513-21334514 - T2940 COSM4696611 c.413T>C p.L138S Substitution - Missense 9:21334447-21334447 - TCGA-BR-4267-01 COSM3906600 c.589C>T p.R197* Substitution - Nonsense 9:21334271-21334271 - TCGA-23-2078-01 COSM78975 c.863C>G p.S288* Substitution - Nonsense 9:21333997-21333997 - TCGA-D1-A16B-01 COSM1107842 c.634G>A p.E212K Substitution - Missense 9:21334226-21334226 - C91 COSM4445196 c.1672C>T p.R558C Substitution - Missense 9:21333188-21333188 - TCGA-DI-A0WH-01 COSM1107837 c.1125G>A p.R375R Substitution - coding silent 9:21333735-21333735 - PCSI_0083_Pa_P_526 COSM3382496 c.288T>G p.H96Q Substitution - Missense 9:21334572-21334572 - TCGA-BR-4184-01 COSM3906597 c.1422G>A p.M474I Substitution - Missense 9:21333438-21333438 - 2521249 COSM5888050 c.748C>T p.L250F Substitution - Missense 9:21334112-21334112 - TCGA-BS-A0TA-01 COSM1107833 c.1586C>T p.A529V Substitution - Missense 9:21333274-21333274 - PCSI_0083_Pa_P_526 COSM3382497 c.278T>G p.I93S Substitution - Missense 9:21334582-21334582 - sysucc-834T COSM5486735 c.180T>C p.D60D Substitution - coding silent 9:21334680-21334680 - LUAD_E00565 COSM389696 c.1249G>C p.E417Q Substitution - Missense 9:21333611-21333611 - TCGA-34-5236-01 COSM753768 c.1300G>A p.E434K Substitution - Missense 9:21333560-21333560 - TCGA-D1-A17S-01 COSM1107834 c.1509C>A p.F503L Substitution - Missense 9:21333351-21333351 - 33 COSM5733395 c.824A>G p.N275S Substitution - Missense 9:21334036-21334036 - 4132_T COSM3952623 c.467A>T p.E156V Substitution - Missense 9:21334393-21334393 - TCGA-B5-A0JY-01 COSM1107846 c.238A>G p.M80V Substitution - Missense 9:21334622-21334622 - TCGA-CA-6717-01 COSM1461777 c.51G>A p.Q17Q Substitution - coding silent 9:21334809-21334809 - TCGA-AN-A046-01 COSM3848263 c.721C>T p.R241* Substitution - Nonsense 9:21334139-21334139 - 5T COSM110672 c.409_410insT p.L138fs*5 Insertion - Frameshift 9:21334450-21334451 - TCGA-D3-A5GU-06 COSM3656585 c.236C>T p.A79V Substitution - Missense 9:21334624-21334624 - 234 COSM3731044 c.659G>A p.C220Y Substitution - Missense 9:21334201-21334201 - 587376 COSM1212690 c.1045C>A p.L349I Substitution - Missense 9:21333815-21333815 - TCGA-59-2352-01 COSM80078 c.1230T>C p.A410A Substitution - coding silent 9:21333630-21333630 - CSCC-7-T COSM4498820 c.528C>T p.F176F Substitution - coding silent 9:21334332-21334332 - TCGA-EE-A2MS-06 COSM3656584 c.532C>T p.L178L Substitution - coding silent 9:21334328-21334328 - CH-109-T2 COSM5650609 c.916G>A p.V306I Substitution - Missense 9:21333944-21333944 - TCGA-DK-A2I4-01 COSM3779928 c.685C>T p.R229W Substitution - Missense 9:21334175-21334175 - PD5951a COSM5791371 c.711G>A p.M237I Substitution - Missense 9:21334149-21334149 - PCSI_0083_Pa_P_526 COSM3382495 c.367C>T p.Q123* Substitution - Nonsense 9:21334493-21334493 - HCT8 COSM4635727 c.1170A>G p.T390T Substitution - coding silent 9:21333690-21333690 - HCT15 COSM3092069 c.846G>A p.M282I Substitution - Missense 9:21334014-21334014 - 65 COSM5011998 c.76T>C p.F26L Substitution - Missense 9:21334784-21334784 - Pat_63_B COSM5876064 c.1801C>T p.P601S Substitution - Missense 9:21333059-21333059 - TCGA-AP-A059-01 COSM1107847 c.139G>T p.G47* Substitution - Nonsense 9:21334721-21334721 - TCGA-EK-A3GK-01 COSM4854430 c.259G>C p.E87Q Substitution - Missense 9:21334601-21334601 - TCGA-HU-A4GT-01 COSM77978 c.1219C>T p.R407C Substitution - Missense 9:21333641-21333641 - TCGA-66-2763-01 COSM753769 c.1684G>C p.E562Q Substitution - Missense 9:21333176-21333176 - PTC-7C COSM4163703 c.1605A>G p.Q535Q Substitution - coding silent 9:21333255-21333255 - TCGA-B8-5550-01 COSM3367674 c.837G>A p.M279I Substitution - Missense 9:21334023-21334023 - 587350 COSM1212689 c.661C>T p.R221C Substitution - Missense 9:21334199-21334199 - EGC15 COSM5063855 c.744G>T p.Q248H Substitution - Missense 9:21334116-21334116 - TCGA-DD-A11A-01 COSM4940372 c.571C>T p.L191L Substitution - coding silent 9:21334289-21334289 - SS6003131 COSM3665377 c.1054G>C p.V352L Substitution - Missense 9:21333806-21333806 - RK208_C01 COSM1636137 c.727C>T p.P243S Substitution - Missense 9:21334133-21334133 - TCGA-AA-A010-01 COSM282289 c.1641C>T p.I547I Substitution - coding silent 9:21333219-21333219 - KM12 COSM1674413 c.115G>A p.G39S Substitution - Missense 9:21334745-21334745 - 587368 COSM1212691 c.1325C>G p.T442R Substitution - Missense 9:21333535-21333535 - TCGA-AN-A046-01 COSM3848264 c.590G>A p.R197Q Substitution - Missense 9:21334270-21334270 - TCGA-BR-8680-01 COSM3906601 c.379G>A p.E127K Substitution - Missense 9:21334481-21334481 - TCGA-BR-4292-01 COSM3906602 c.66A>G p.G22G Substitution - coding silent 9:21334794-21334794 - TCGA-D8-A1XK-01 COSM3848265 c.480T>C p.I160I Substitution - coding silent 9:21334380-21334380 - B59-Tumor COSM1756108 c.181G>A p.E61K Substitution - Missense 9:21334679-21334679 - TCGA-BR-6452-01 COSM3906596 c.1736A>T p.D579V Substitution - Missense 9:21333124-21333124 - TCGA-22-1016-01 COSM753767 c.1220G>T p.R407L Substitution - Missense 9:21333640-21333640 - B59 COSM1756108 c.181G>A p.E61K Substitution - Missense 9:21334679-21334679 - TCGA-BR-4361-01 COSM3906599 c.965A>G p.E322G Substitution - Missense 9:21333895-21333895 - PCSI_0083_Pa_X COSM3382496 c.288T>G p.H96Q Substitution - Missense 9:21334572-21334572 - PCSI_0083_Pa_P COSM3382495 c.367C>T p.Q123* Substitution - Nonsense 9:21334493-21334493 - TCGA-AZ-4315-01 COSM1461772 c.976G>T p.E326* Substitution - Nonsense 9:21333884-21333884 - ESCC_9 COSM5623695 c.193G>C p.V65L Substitution - Missense 9:21334667-21334667 - KM12 COSM1674413 c.115G>A p.G39S Substitution - Missense 9:21334745-21334745 - TCGA-AG-3892-01 COSM257249 c.1234G>T p.E412* Substitution - Nonsense 9:21333626-21333626 - TCGA-24-1418-01 COSM117190 c.1742C>T p.P581L Substitution - Missense 9:21333118-21333118 - TCGA-AN-A046-01 COSM1107842 c.634G>A p.E212K Substitution - Missense 9:21334226-21334226 - TCGA-AX-A0J0-01 COSM1107843 c.314A>C p.K105T Substitution - Missense 9:21334546-21334546 - YUBER COSM1700986 c.608C>T p.S203F Substitution - Missense 9:21334252-21334252 - TCGA-DD-A4NS-01 COSM4926362 c.287A>C p.H96P Substitution - Missense 9:21334573-21334573 - T3557 COSM4696609 c.1690G>T p.V564F Substitution - Missense 9:21333170-21333170 - TCGA-57-1582-01 COSM77978 c.1219C>T p.R407C Substitution - Missense 9:21333641-21333641 - TCGA-BR-8680-01 COSM3906598 c.1165C>T p.R389C Substitution - Missense 9:21333695-21333695 - RK056_C01 COSM1636138 c.83C>T p.T28I Substitution - Missense 9:21334777-21334777 - TCGA-D1-A103-01 COSM1107832 c.1705C>A p.P569T Substitution - Missense 9:21333155-21333155 - TCGA-AA-3492-01 COSM1461774 c.432_435delTCTT p.F144fs*23 Deletion - Frameshift 9:21334425-21334428 - TCGA-AP-A0LT-01 COSM1107835 c.1464G>A p.M488I Substitution - Missense 9:21333396-21333396 - PT46 COSM5929115 c.976G>A p.E326K Substitution - Missense 9:21333884-21333884 - TCGA-A5-A0R7-01 COSM1107838 c.1105G>A p.V369I Substitution - Missense 9:21333755-21333755 - TCGA-LL-A50Y-01 COSM3848262 c.1743A>T p.P581P Substitution - coding silent 9:21333117-21333117 - PCSI_0083_Pa_P COSM3382496 c.288T>G p.H96Q Substitution - Missense 9:21334572-21334572 - CHEWS029 COSM4588740 c.1009C>T p.R337C Substitution - Missense 9:21333851-21333851 - TCGA-HU-A4GQ-01 COSM1107837 c.1125G>A p.R375R Substitution - coding silent 9:21333735-21333735 - TCGA-DI-A0WH-01 COSM1107836 c.1289C>T p.A430V Substitution - Missense 9:21333571-21333571 - TCGA-AA-A00N-01 COSM275768 c.722G>A p.R241Q Substitution - Missense 9:21334138-21334138 - BK0035 COSM4187069 c.190C>A p.P64T Substitution - Missense 9:21334670-21334670 - TCGA-D1-A17H-01 COSM1107839 c.1104A>T p.T368T Substitution - coding silent 9:21333756-21333756 - PT13 COSM5896006 c.1680G>A p.M560I Substitution - Missense 9:21333180-21333180 - 2217535 COSM4421686 c.220A>C p.S74R Substitution - Missense 9:21334640-21334640 - T407 COSM4696610 c.1580delC p.P527fs*6 Deletion - Frameshift 9:21333280-21333280 - Pat_06_B COSM5876065 c.604C>T p.L202F Substitution - Missense 9:21334256-21334256 - ESO-1488 COSM1256006 c.1347T>A p.Y449* Substitution - Nonsense 9:21333513-21333513 - TCGA-DM-A285-01 COSM1461775 c.231C>G p.F77L Substitution - Missense 9:21334629-21334629 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.701719;Hs.701722;Hs.701723;Hs.701726;Hs.701732;Hs.701738;Hs.701745;Hs.701747;Hs.701753;Hs.701775;Hs.701778 9p22 610606;611201 Hs.710126 9p22 611201 Hs.731840;Hs.731841;Hs.731842;Hs.731843 9p22 611201

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer AA - Frameshift p.L151Gfs*2 c.451_452delTT 9 21334407 PRAD A C Missense p.L213R c.638T>G 9 21334221 CM A G Missense p.L223P c.668T>C 9 21334191 CM A G Missense p.Y509H c.1525T>C 9 21333334 LUAD A G Synonymous p.A410A c.1230T>C 9 21333629 OV A G Synonymous p.L43L c.129T>C 9 21334730 LUAD A T Nonsense p.Y449* c.1347T>A 9 21333512 ESCA C A Missense p.D231Y c.691G>T 9 21334168 LUAD C A Missense p.R407L c.1220G>T 9 21333639 LUSC C G Missense p.E562Q c.1684G>C 9 21333175 LUSC C G Missense p.G354A c.1061G>C 9 21333798 LUAD C G Missense p.Q255H c.765G>C 9 21334094 CM C T Missense p.D289N c.865G>A 9 21333994 LUSC C T Missense p.E434K c.1300G>A 9 21333559 LUSC C T Missense p.M279I c.837G>A 9 21334022 RCCC C T Missense p.M488I c.1464G>A 9 21333395 UCEC C T Synonymous p.R375R c.1125G>A 9 21333734 UCEC G A Missense p.A430V c.1289C>T 9 21333570 UCEC G A Missense p.A529V c.1586C>T 9 21333273 UCEC G A Missense p.P332S c.994C>T 9 21333865 LGG G A Missense p.P581L c.1742C>T 9 21333117 OV G A Missense p.P596S c.1786C>T 9 21333073 CM G A Missense p.R229W c.685C>T 9 21334174 BLCA G A Missense p.R375W c.1123C>T 9 21333736 HNSC G A Missense p.R407C c.1219C>T 9 21333640 OV G A Missense p.T28I c.83C>T 9 21334776 HC G A Nonsense p.R197* c.589C>T 9 21334270 STAD G A Synonymous p.G11G c.33C>T 9 21334826 LUAD G A Synonymous p.L178L c.532C>T 9 21334327 CM G C Nonsense p.S288* c.863C>G 9 21333996 OV GG TT Missense p.R337S c.1008_1009delinsAA 9 21333850 CM T A Synonymous p.T368T c.1104A>T 9 21333755 UCEC T C Missense p.D60G c.179A>G 9 21334680 LUAD T C Missense p.K2E c.4A>G 9 21334855 LUSC T C Missense p.Q88R c.263A>G 9 21334596 BLCA T C Synonymous p.G22G c.66A>G 9 21334793 STAD