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 9 119460913 119460913 + Missense_Mutation SNP C C G TCGA-OR-A5L2-01A-11D-A30A-10 TCGA-OR-A5L2-10A-01D-A30A-10 g.chr9:119460913C>G c.892C>G c.(892-894)Ccc>Gcc p.P298A BLCA 9 119460240 119460240 + Missense_Mutation SNP G G C TCGA-K4-A54R-01A-11D-A26M-08 TCGA-K4-A54R-10A-01D-A26K-08 g.chr9:119460240G>C c.219G>C c.(217-219)ttG>ttC p.L73F BLCA 9 119460323 119460323 + Missense_Mutation SNP G G A TCGA-DK-A1AB-01A-11D-A13W-08 TCGA-DK-A1AB-10A-01D-A13W-08 g.chr9:119460323G>A c.302G>A c.(301-303)cGg>cAg p.R101Q BLCA 9 119460354 119460354 + Silent SNP C C T TCGA-UY-A9PH-01A-11D-A38G-08 TCGA-UY-A9PH-10A-01D-A38J-08 g.chr9:119460354C>T c.333C>T c.(331-333)ttC>ttT p.F111F BLCA 9 119460715 119460715 + Missense_Mutation SNP G G A TCGA-XF-AAN2-01A-11D-A42E-08 TCGA-XF-AAN2-10A-01D-A42H-08 g.chr9:119460715G>A c.694G>A c.(694-696)Gag>Aag p.E232K BLCA 9 119461344 119461344 + Silent SNP G G A TCGA-GV-A3JZ-01A-11D-A21A-08 TCGA-GV-A3JZ-10A-01D-A21A-08 g.chr9:119461344G>A c.1323G>A c.(1321-1323)ctG>ctA p.L441L BLCA 9 119461693 119461693 + Missense_Mutation SNP G G A TCGA-DK-AA76-01A-11D-A391-08 TCGA-DK-AA76-10A-01D-A394-08 g.chr9:119461693G>A c.1672G>A c.(1672-1674)Gat>Aat p.D558N BLCA 9 119461874 119461874 + Missense_Mutation SNP G G A TCGA-CU-A3YL-01A-11D-A22Z-08 TCGA-CU-A3YL-10A-01D-A22Z-08 g.chr9:119461874G>A c.1853G>A c.(1852-1854)tGt>tAt p.C618Y BRCA 9 119460255 119460255 + Missense_Mutation SNP C C G TCGA-EW-A1OZ-01A-11D-A142-09 TCGA-EW-A1OZ-10A-01D-A142-09 g.chr9:119460255C>G c.234C>G c.(232-234)gaC>gaG p.D78E BRCA 9 119460572 119460572 + Missense_Mutation SNP T T A TCGA-AR-A254-01A-21D-A167-09 TCGA-AR-A254-10A-01D-A167-09 g.chr9:119460572T>A c.551T>A c.(550-552)gTt>gAt p.V184D BRCA 9 119460577 119460577 + Nonsense_Mutation SNP C C T TCGA-BH-A0HA-01A-11D-A12Q-09 TCGA-BH-A0HA-11A-31D-A12Q-09 g.chr9:119460577C>T c.556C>T c.(556-558)Cag>Tag p.Q186* CESC 9 119460693 119460693 + Missense_Mutation SNP G G C TCGA-Q1-A6DT-01A-11D-A32I-09 TCGA-Q1-A6DT-10A-01D-A32I-09 g.chr9:119460693G>C c.672G>C c.(670-672)caG>caC p.Q224H CHOL 9 119461766 119461766 + Missense_Mutation SNP G G T TCGA-4G-AAZO-01A-12D-A417-09 TCGA-4G-AAZO-11A-11D-A41A-09 g.chr9:119461766G>T c.1745G>T c.(1744-1746)tGt>tTt p.C582F COAD 9 119460416 119460416 + Missense_Mutation SNP G G A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr9:119460416G>A c.395G>A c.(394-396)gGc>gAc p.G132D COAD 9 119460676 119460676 + Nonsense_Mutation SNP C C T TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr9:119460676C>T c.655C>T c.(655-657)Caa>Taa p.Q219* COAD 9 119460703 119460703 + Missense_Mutation SNP C C T TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr9:119460703C>T c.682C>T c.(682-684)Ctt>Ttt p.L228F COAD 9 119461145 119461145 + Missense_Mutation SNP T T G TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr9:119461145T>G c.1124T>G c.(1123-1125)gTc>gGc p.V375G COAD 9 119461168 119461168 + Missense_Mutation SNP G G T TCGA-AA-3522-01A-01W-0831-10 TCGA-AA-3522-10A-01W-0831-10 g.chr9:119461168G>T c.1147G>T c.(1147-1149)Ggt>Tgt p.G383C COAD 9 119461597 119461597 + Missense_Mutation SNP A A G TCGA-G4-6299-01A-11D-1771-10 TCGA-G4-6299-10A-01D-1771-10 g.chr9:119461597A>G c.1576A>G c.(1576-1578)Acc>Gcc p.T526A COAD 9 119461598 119461598 + Missense_Mutation SNP C C T TCGA-AA-3968-01A-01W-0995-10 TCGA-AA-3968-10A-01W-0995-10 g.chr9:119461598C>T c.1577C>T c.(1576-1578)aCc>aTc p.T526I COAD 9 119461599 119461599 + Silent SNP C C A TCGA-G4-6323-01A-11D-1719-10 TCGA-G4-6323-10A-01D-1720-10 g.chr9:119461599C>A c.1578C>A c.(1576-1578)acC>acA p.T526T COAD 9 119461660 119461660 + Nonsense_Mutation SNP G G T TCGA-F4-6808-01A-11D-1835-10 TCGA-F4-6808-10A-01D-1835-10 g.chr9:119461660G>T c.1639G>T c.(1639-1641)Gag>Tag p.E547* COAD 9 119461661 119461661 + Missense_Mutation SNP A A G TCGA-AZ-5403-01A-01D-1650-10 TCGA-AZ-5403-10A-01D-1650-10 g.chr9:119461661A>G c.1640A>G c.(1639-1641)gAg>gGg p.E547G COAD 9 119461661 119461661 + Missense_Mutation SNP A A G TCGA-G4-6304-01A-11D-1924-10 TCGA-G4-6304-10A-01D-1924-10 g.chr9:119461661A>G c.1640A>G c.(1639-1641)gAg>gGg p.E547G COAD 9 119461944 119461944 + Missense_Mutation SNP G G C TCGA-G4-6315-01A-11D-1719-10 TCGA-G4-6315-10A-01D-1720-10 g.chr9:119461944G>C c.1923G>C c.(1921-1923)aaG>aaC p.K641N COAD 9 119461982 119461983 + Stop_Codon_Ins INS - - T TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr9:119461982_119461983insT COADREAD 9 119460416 119460416 + Missense_Mutation SNP G G A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr9:119460416G>A c.395G>A c.(394-396)gGc>gAc p.G132D COADREAD 9 119460676 119460676 + Nonsense_Mutation SNP C C T TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr9:119460676C>T c.655C>T c.(655-657)Caa>Taa p.Q219* COADREAD 9 119460703 119460703 + Missense_Mutation SNP C C T TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr9:119460703C>T c.682C>T c.(682-684)Ctt>Ttt p.L228F COADREAD 9 119461145 119461145 + Missense_Mutation SNP T T G TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr9:119461145T>G c.1124T>G c.(1123-1125)gTc>gGc p.V375G COADREAD 9 119461168 119461168 + Missense_Mutation SNP G G T TCGA-AA-3522-01A-01W-0831-10 TCGA-AA-3522-10A-01W-0831-10 g.chr9:119461168G>T c.1147G>T c.(1147-1149)Ggt>Tgt p.G383C COADREAD 9 119461597 119461597 + Missense_Mutation SNP A A G TCGA-G4-6299-01A-11D-1771-10 TCGA-G4-6299-10A-01D-1771-10 g.chr9:119461597A>G c.1576A>G c.(1576-1578)Acc>Gcc p.T526A COADREAD 9 119461598 119461598 + Missense_Mutation SNP C C T TCGA-AA-3968-01A-01W-0995-10 TCGA-AA-3968-10A-01W-0995-10 g.chr9:119461598C>T c.1577C>T c.(1576-1578)aCc>aTc p.T526I COADREAD 9 119461599 119461599 + Silent SNP C C A TCGA-G4-6323-01A-11D-1719-10 TCGA-G4-6323-10A-01D-1720-10 g.chr9:119461599C>A c.1578C>A c.(1576-1578)acC>acA p.T526T COADREAD 9 119461660 119461660 + Nonsense_Mutation SNP G G T TCGA-F4-6808-01A-11D-1835-10 TCGA-F4-6808-10A-01D-1835-10 g.chr9:119461660G>T c.1639G>T c.(1639-1641)Gag>Tag p.E547* COADREAD 9 119461661 119461661 + Missense_Mutation SNP A A G TCGA-AZ-5403-01A-01D-1650-10 TCGA-AZ-5403-10A-01D-1650-10 g.chr9:119461661A>G c.1640A>G c.(1639-1641)gAg>gGg p.E547G COADREAD 9 119461661 119461661 + Missense_Mutation SNP A A G TCGA-G4-6304-01A-11D-1924-10 TCGA-G4-6304-10A-01D-1924-10 g.chr9:119461661A>G c.1640A>G c.(1639-1641)gAg>gGg p.E547G COADREAD 9 119461944 119461944 + Missense_Mutation SNP G G C TCGA-G4-6315-01A-11D-1719-10 TCGA-G4-6315-10A-01D-1720-10 g.chr9:119461944G>C c.1923G>C c.(1921-1923)aaG>aaC p.K641N COADREAD 9 119461982 119461983 + Stop_Codon_Ins INS - - T TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr9:119461982_119461983insT ESCA 9 119460513 119460513 + Silent SNP G G A TCGA-2H-A9GK-01A-11D-A37C-09 TCGA-2H-A9GK-11A-11D-A37F-09 g.chr9:119460513G>A c.492G>A c.(490-492)caG>caA p.Q164Q ESCA 9 119461051 119461051 + Missense_Mutation SNP C C T TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr9:119461051C>T c.1030C>T c.(1030-1032)Cgg>Tgg p.R344W GBM 9 119461599 119461599 + Silent SNP C C T TCGA-06-0128-01A-01D-1490-08 TCGA-06-0128-10A-01D-1490-08 g.chr9:119461599C>T c.1578C>T c.(1576-1578)acC>acT p.T526T GBMLGG 9 119461189 119461189 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:119461189C>T c.1168C>T c.(1168-1170)Cgt>Tgt p.R390C GBMLGG 9 119461244 119461244 + Missense_Mutation SNP G G A TCGA-E1-5307-01A-01D-1893-08 TCGA-E1-5307-10A-01D-1893-08 g.chr9:119461244G>A c.1223G>A c.(1222-1224)cGc>cAc p.R408H GBMLGG 9 119461599 119461599 + Silent SNP C C T TCGA-06-0128-01A-01D-1490-08 TCGA-06-0128-10A-01D-1490-08 g.chr9:119461599C>T c.1578C>T c.(1576-1578)acC>acT p.T526T HNSC 9 119460324 119460324 + Silent SNP G G T TCGA-CV-A45W-01A-11D-A25D-08 TCGA-CV-A45W-10A-01D-A25E-08 g.chr9:119460324G>T c.303G>T c.(301-303)cgG>cgT p.R101R HNSC 9 119460354 119460354 + Silent SNP C C T TCGA-CV-7427-01A-11D-2078-08 TCGA-CV-7427-10A-01D-2078-08 g.chr9:119460354C>T c.333C>T c.(331-333)ttC>ttT p.F111F HNSC 9 119461060 119461060 + Missense_Mutation SNP G G A TCGA-WA-A7GZ-01A-11D-A34J-08 TCGA-WA-A7GZ-10A-01D-A34M-08 g.chr9:119461060G>A c.1039G>A c.(1039-1041)Gag>Aag p.E347K HNSC 9 119461243 119461243 + Missense_Mutation SNP C C T TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr9:119461243C>T c.1222C>T c.(1222-1224)Cgc>Tgc p.R408C HNSC 9 119461731 119461731 + Silent SNP G G A TCGA-CV-A468-01A-11D-A25Y-08 TCGA-CV-A468-10A-01D-A25Y-08 g.chr9:119461731G>A c.1710G>A c.(1708-1710)tcG>tcA p.S570S HNSC 9 119461761 119461761 + Silent SNP C C T TCGA-CV-7235-01A-11D-2012-08 TCGA-CV-7235-10A-01D-2013-08 g.chr9:119461761C>T c.1740C>T c.(1738-1740)ggC>ggT p.G580G HNSC 9 119461806 119461806 + Silent SNP T T C TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr9:119461806T>C c.1785T>C c.(1783-1785)agT>agC p.S595S KIPAN 9 119460981 119460981 + Silent SNP T T C TCGA-A3-3373-01A-02D-1421-08 TCGA-A3-3373-11A-01D-1421-08 g.chr9:119460981T>C c.960T>C c.(958-960)gtT>gtC p.V320V KIRC 9 119460981 119460981 + Silent SNP T T C TCGA-A3-3373-01A-02D-1421-08 TCGA-A3-3373-11A-01D-1421-08 g.chr9:119460981T>C c.960T>C c.(958-960)gtT>gtC p.V320V LGG 9 119461189 119461189 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:119461189C>T c.1168C>T c.(1168-1170)Cgt>Tgt p.R390C LGG 9 119461244 119461244 + Missense_Mutation SNP G G A TCGA-E1-5307-01A-01D-1893-08 TCGA-E1-5307-10A-01D-1893-08 g.chr9:119461244G>A c.1223G>A c.(1222-1224)cGc>cAc p.R408H LIHC 9 119460448 119460448 + Missense_Mutation SNP G G A TCGA-WQ-AB4B-01A-11D-A40P-10 TCGA-WQ-AB4B-10A-01D-A40P-10 g.chr9:119460448G>A c.427G>A c.(427-429)Gag>Aag p.E143K LIHC 9 119461528 119461528 + Frame_Shift_Del DEL G G - TCGA-DD-A39Y-01A-11D-A20W-10 TCGA-DD-A39Y-11A-11D-A20W-10 g.chr9:119461528delG c.1507delG c.(1507-1509)gggfs p.G503fs LIHC 9 119461915 119461915 + Missense_Mutation SNP G G T TCGA-DD-AADL-01A-11D-A40R-10 TCGA-DD-AADL-10A-01D-A40U-10 g.chr9:119461915G>T c.1894G>T c.(1894-1896)Gtc>Ttc p.V632F LUAD 9 119460463 119460463 + Missense_Mutation SNP G G T TCGA-05-4382-01A-01D-1931-08 TCGA-05-4382-10A-01D-1265-08 g.chr9:119460463G>T c.442G>T c.(442-444)Gac>Tac p.D148Y LUAD 9 119461127 119461127 + Missense_Mutation SNP G G A TCGA-55-8302-01A-11D-2323-08 TCGA-55-8302-10A-01D-2323-08 g.chr9:119461127G>A c.1106G>A c.(1105-1107)gGa>gAa p.G369E LUAD 9 119461837 119461837 + Missense_Mutation SNP G G A TCGA-MP-A4TF-01A-11D-A25L-08 TCGA-MP-A4TF-10A-01D-A25L-08 g.chr9:119461837G>A c.1816G>A c.(1816-1818)Ggg>Agg p.G606R LUSC 9 119460298 119460298 + Nonsense_Mutation SNP G G T TCGA-34-2600-01A-01D-1522-08 TCGA-34-2600-11A-01D-1522-08 g.chr9:119460298G>T c.277G>T c.(277-279)Gag>Tag p.E93* LUSC 9 119460833 119460833 + Missense_Mutation SNP G G A TCGA-66-2759-01A-01D-1522-08 TCGA-66-2759-11A-01D-1522-08 g.chr9:119460833G>A c.812G>A c.(811-813)cGg>cAg p.R271Q LUSC 9 119461418 119461418 + Missense_Mutation SNP G G T TCGA-46-3765-01A-01D-0983-08 TCGA-46-3765-10A-01D-0983-08 g.chr9:119461418G>T c.1397G>T c.(1396-1398)aGg>aTg p.R466M LUSC 9 119461837 119461837 + Missense_Mutation SNP G G T TCGA-33-4532-01A-01D-1267-08 TCGA-33-4532-11A-01D-1267-08 g.chr9:119461837G>T c.1816G>T c.(1816-1818)Ggg>Tgg p.G606W OV 9 119460735 119460735 + Silent SNP C C T TCGA-29-1769-01A-01W-0639-09 TCGA-29-1769-10A-01W-0639-09 g.chr9:119460735C>T c.714C>T c.(712-714)cgC>cgT p.R238R PAAD 9 119461183 119461183 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:119461183G>A c.1162G>A c.(1162-1164)Gct>Act p.A388T PAAD 9 119461253 119461253 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:119461253C>T c.1232C>T c.(1231-1233)cCc>cTc p.P411L PRAD 9 119461051 119461051 + Missense_Mutation SNP C C T TCGA-CH-5769-01A-11D-1576-08 TCGA-CH-5769-11A-01D-1576-08 g.chr9:119461051C>T c.1030C>T c.(1030-1032)Cgg>Tgg p.R344W SKCM 9 119460032 119460032 + Missense_Mutation SNP C C T TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr9:119460032C>T c.11C>T c.(10-12)gCa>gTa p.A4V SKCM 9 119460989 119460989 + Missense_Mutation SNP G G C TCGA-EE-A3AF-06A-11D-A196-08 TCGA-EE-A3AF-10A-01D-A198-08 g.chr9:119460989G>C c.968G>C c.(967-969)aGa>aCa p.R323T SKCM 9 119461105 119461105 + Missense_Mutation SNP G G A TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr9:119461105G>A c.1084G>A c.(1084-1086)Ggg>Agg p.G362R SKCM 9 119461141 119461141 + Missense_Mutation SNP C C T TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr9:119461141C>T c.1120C>T c.(1120-1122)Cca>Tca p.P374S SKCM 9 119461243 119461243 + Missense_Mutation SNP C C A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr9:119461243C>A c.1222C>A c.(1222-1224)Cgc>Agc p.R408S SKCM 9 119461313 119461313 + Missense_Mutation SNP C C T TCGA-EE-A2GR-06A-11D-A197-08 TCGA-EE-A2GR-10A-01D-A199-08 g.chr9:119461313C>T c.1292C>T c.(1291-1293)cCt>cTt p.P431L SKCM 9 119461791 119461791 + Silent SNP C C T TCGA-D3-A2JN-06A-11D-A196-08 TCGA-D3-A2JN-10A-01D-A198-08 g.chr9:119461791C>T c.1770C>T c.(1768-1770)atC>atT p.I590I

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 119459957 119459957 single base substitution T G 5_prime_UTR_variant BLCA-CN 9 119461150 119461150 single base substitution C T downstream_gene_variant BLCA-CN 9 119461150 119461150 single base substitution C T missense_variant L377F 1129C>T BLCA-US 9 119460323 119460323 single base substitution G A missense_variant R101Q 302G>A BLCA-US 9 119461344 119461344 single base substitution G A downstream_gene_variant BLCA-US 9 119461344 119461344 single base substitution G A synonymous_variant L441L 1323G>A BLCA-US 9 119461874 119461874 single base substitution G A downstream_gene_variant BLCA-US 9 119461874 119461874 single base substitution G A missense_variant C618Y 1853G>A BRCA-EU 9 119445121 119445121 single base substitution C T upstream_gene_variant BRCA-EU 9 119445638 119445638 single base substitution C A upstream_gene_variant BRCA-EU 9 119446795 119446795 single base substitution C T upstream_gene_variant BRCA-EU 9 119447013 119447013 single base substitution G A upstream_gene_variant BRCA-EU 9 119448589 119448589 single base substitution T G upstream_gene_variant BRCA-EU 9 119448853 119448853 single base substitution C T upstream_gene_variant BRCA-EU 9 119449286 119449286 single base substitution G A upstream_gene_variant BRCA-EU 9 119449579 119449579 deletion of <=200bp G - upstream_gene_variant BRCA-EU 9 119449987 119449987 single base substitution G C intron_variant BRCA-EU 9 119451387 119451387 deletion of <=200bp C - intron_variant BRCA-EU 9 119452115 119452115 single base substitution G C intron_variant BRCA-EU 9 119454178 119454178 single base substitution C A intron_variant BRCA-EU 9 119454549 119454549 single base substitution C G intron_variant BRCA-EU 9 119455587 119455587 single base substitution G C intron_variant BRCA-EU 9 119458287 119458287 single base substitution C T intron_variant BRCA-EU 9 119460828 119460828 single base substitution G A downstream_gene_variant BRCA-EU 9 119460828 119460828 single base substitution G A synonymous_variant L269L 807G>A BRCA-EU 9 119461299 119461299 single base substitution A T downstream_gene_variant BRCA-EU 9 119461299 119461299 single base substitution A T synonymous_variant L426L 1278A>T BRCA-EU 9 119466011 119466011 insertion of <=200bp - T downstream_gene_variant BRCA-EU 9 119467416 119467416 single base substitution T C downstream_gene_variant BRCA-EU 9 119467641 119467641 single base substitution A T downstream_gene_variant BRCA-FR 9 119458287 119458287 single base substitution C T intron_variant BRCA-FR 9 119464576 119464576 single base substitution G A downstream_gene_variant BRCA-UK 9 119461947 119461947 single base substitution C T downstream_gene_variant BRCA-UK 9 119461947 119461947 single base substitution C T synonymous_variant I642I 1926C>T BRCA-US 9 119460255 119460255 single base substitution C G missense_variant D78E 234C>G BRCA-US 9 119460572 119460572 single base substitution T A downstream_gene_variant BRCA-US 9 119460572 119460572 single base substitution T A missense_variant V184D 551T>A BRCA-US 9 119460577 119460577 single base substitution C T downstream_gene_variant BRCA-US 9 119460577 119460577 single base substitution C T stop_gained Q186* 556C>T BTCA-JP 9 119460065 119460065 single base substitution G A missense_variant R15Q 44G>A BTCA-JP 9 119461545 119461545 insertion of <=200bp - CT downstream_gene_variant BTCA-JP 9 119461545 119461545 insertion of <=200bp - CT frameshift_variant S508S? CESC-US 9 119460693 119460693 single base substitution G C downstream_gene_variant CESC-US 9 119460693 119460693 single base substitution G C missense_variant Q224H 672G>C CLLE-ES 9 119463923 119463923 insertion of <=200bp - ACAA downstream_gene_variant COAD-US 9 119448979 119448979 single base substitution C T upstream_gene_variant COAD-US 9 119461275 119461275 single base substitution G A downstream_gene_variant COAD-US 9 119461275 119461275 single base substitution G A synonymous_variant V418V 1254G>A COAD-US 9 119461791 119461791 single base substitution C T downstream_gene_variant COAD-US 9 119461791 119461791 single base substitution C T synonymous_variant I590I 1770C>T COAD-US 9 119461944 119461944 single base substitution G C downstream_gene_variant COAD-US 9 119461944 119461944 single base substitution G C missense_variant K641N 1923G>C COAD-US 9 119461982 119461982 insertion of <=200bp - T downstream_gene_variant COAD-US 9 119461982 119461982 insertion of <=200bp - T frameshift_variant *654L? COAD-US 9 119463493 119463493 deletion of <=200bp T - 3_prime_UTR_variant COAD-US 9 119463493 119463493 deletion of <=200bp T - downstream_gene_variant COCA-CN 9 119449230 119449230 single base substitution G C upstream_gene_variant COCA-CN 9 119456954 119456954 single base substitution C G intron_variant COCA-CN 9 119460002 119460002 single base substitution T A 5_prime_UTR_variant COCA-CN 9 119460118 119460118 single base substitution C T missense_variant R33C 97C>T COCA-CN 9 119460404 119460404 single base substitution A G missense_variant H128R 383A>G COCA-CN 9 119461210 119461210 single base substitution G A downstream_gene_variant COCA-CN 9 119461210 119461210 single base substitution G A missense_variant V397I 1189G>A ESAD-UK 9 119445588 119445588 single base substitution T C upstream_gene_variant ESAD-UK 9 119445808 119445808 single base substitution G C upstream_gene_variant ESAD-UK 9 119447277 119447277 single base substitution C T upstream_gene_variant ESAD-UK 9 119447859 119447859 single base substitution G T upstream_gene_variant ESAD-UK 9 119448117 119448117 single base substitution C G upstream_gene_variant ESAD-UK 9 119449120 119449120 single base substitution G A upstream_gene_variant ESAD-UK 9 119450794 119450794 single base substitution C T intron_variant ESAD-UK 9 119453545 119453545 single base substitution G A intron_variant ESAD-UK 9 119453996 119453996 single base substitution C A intron_variant ESAD-UK 9 119454560 119454560 single base substitution T G intron_variant ESAD-UK 9 119457109 119457109 single base substitution G A intron_variant ESAD-UK 9 119457564 119457564 single base substitution A G intron_variant ESAD-UK 9 119458843 119458843 single base substitution A G intron_variant ESAD-UK 9 119459012 119459012 single base substitution G C intron_variant ESAD-UK 9 119460354 119460354 single base substitution C G missense_variant F111L 333C>G ESAD-UK 9 119461520 119461520 single base substitution G A downstream_gene_variant ESAD-UK 9 119461520 119461520 single base substitution G A missense_variant R500Q 1499G>A ESAD-UK 9 119464438 119464438 single base substitution T A downstream_gene_variant ESAD-UK 9 119467328 119467328 single base substitution A T downstream_gene_variant ESAD-UK 9 119468487 119468487 single base substitution T A downstream_gene_variant GBM-US 9 119461599 119461599 single base substitution C T downstream_gene_variant GBM-US 9 119461599 119461599 single base substitution C T synonymous_variant T526T 1578C>T KIRC-US 9 119460981 119460981 single base substitution T C downstream_gene_variant KIRC-US 9 119460981 119460981 single base substitution T C synonymous_variant V320V 960T>C KIRP-US 9 119461631 119461631 single base substitution T A downstream_gene_variant KIRP-US 9 119461631 119461631 single base substitution T A missense_variant L537Q 1610T>A LGG-US 9 119461244 119461244 single base substitution G A downstream_gene_variant LGG-US 9 119461244 119461244 single base substitution G A missense_variant R408H 1223G>A LICA-FR 9 119445311 119445311 insertion of <=200bp - AATAA upstream_gene_variant LICA-FR 9 119446800 119446800 single base substitution C T upstream_gene_variant LICA-FR 9 119459230 119459231 deletion of <=200bp AA - intron_variant LINC-JP 9 119452359 119452359 single base substitution A G intron_variant LINC-JP 9 119454544 119454544 single base substitution A G intron_variant LINC-JP 9 119461545 119461545 insertion of <=200bp - CT downstream_gene_variant LINC-JP 9 119461545 119461545 insertion of <=200bp - CT frameshift_variant S508S? LINC-JP 9 119461945 119461945 single base substitution A G downstream_gene_variant LINC-JP 9 119461945 119461945 single base substitution A G missense_variant I642V 1924A>G LINC-JP 9 119467526 119467526 single base substitution G A downstream_gene_variant LIRI-JP 9 119446250 119446250 single base substitution C G upstream_gene_variant LIRI-JP 9 119446612 119446612 single base substitution T C upstream_gene_variant LIRI-JP 9 119446987 119446987 single base substitution C T upstream_gene_variant LIRI-JP 9 119449083 119449083 single base substitution A C upstream_gene_variant LIRI-JP 9 119452228 119452228 single base substitution A G intron_variant LIRI-JP 9 119454000 119454000 single base substitution A G intron_variant LIRI-JP 9 119455475 119455475 single base substitution A T intron_variant LIRI-JP 9 119462661 119462661 single base substitution A C 3_prime_UTR_variant LIRI-JP 9 119462661 119462661 single base substitution A C downstream_gene_variant LIRI-JP 9 119465075 119465075 insertion of <=200bp - T downstream_gene_variant LIRI-JP 9 119465244 119465244 insertion of <=200bp - T downstream_gene_variant LIRI-JP 9 119465477 119465477 single base substitution G C downstream_gene_variant LIRI-JP 9 119466792 119466792 single base substitution A G downstream_gene_variant LIRI-JP 9 119466965 119466965 single base substitution G T downstream_gene_variant LIRI-JP 9 119467153 119467153 single base substitution A G downstream_gene_variant LIRI-JP 9 119468076 119468076 single base substitution A G downstream_gene_variant LUSC-KR 9 119444673 119444673 single base substitution G A upstream_gene_variant LUSC-KR 9 119445908 119445908 single base substitution T C upstream_gene_variant LUSC-KR 9 119446508 119446508 single base substitution C G upstream_gene_variant LUSC-KR 9 119449470 119449470 single base substitution G C upstream_gene_variant LUSC-KR 9 119451916 119451916 single base substitution A G intron_variant LUSC-KR 9 119461275 119461275 single base substitution G A downstream_gene_variant LUSC-KR 9 119461275 119461275 single base substitution G A synonymous_variant V418V 1254G>A LUSC-KR 9 119463150 119463150 single base substitution C A 3_prime_UTR_variant LUSC-KR 9 119463150 119463150 single base substitution C A downstream_gene_variant LUSC-KR 9 119465170 119465170 single base substitution A G downstream_gene_variant LUSC-KR 9 119465192 119465192 single base substitution G T downstream_gene_variant LUSC-KR 9 119467613 119467613 single base substitution A G downstream_gene_variant LUSC-US 9 119460298 119460298 single base substitution G T stop_gained E93* 277G>T LUSC-US 9 119460833 119460833 single base substitution G A downstream_gene_variant LUSC-US 9 119460833 119460833 single base substitution G A missense_variant R271Q 812G>A LUSC-US 9 119461418 119461418 single base substitution G T downstream_gene_variant LUSC-US 9 119461418 119461418 single base substitution G T missense_variant R466M 1397G>T LUSC-US 9 119461837 119461837 single base substitution G T downstream_gene_variant LUSC-US 9 119461837 119461837 single base substitution G T missense_variant G606W 1816G>T MALY-DE 9 119459446 119459446 single base substitution C T intron_variant MELA-AU 9 119446140 119446140 single base substitution G A upstream_gene_variant MELA-AU 9 119449244 119449244 single base substitution C T upstream_gene_variant MELA-AU 9 119451077 119451077 single base substitution C A intron_variant MELA-AU 9 119451195 119451195 single base substitution G A intron_variant MELA-AU 9 119451932 119451932 single base substitution C T intron_variant MELA-AU 9 119452372 119452372 single base substitution C T intron_variant MELA-AU 9 119453413 119453413 single base substitution C T intron_variant MELA-AU 9 119455711 119455711 single base substitution A T intron_variant MELA-AU 9 119456638 119456638 single base substitution C T intron_variant MELA-AU 9 119456775 119456775 single base substitution C T intron_variant MELA-AU 9 119456830 119456830 single base substitution C T intron_variant MELA-AU 9 119458487 119458487 single base substitution C T intron_variant MELA-AU 9 119458753 119458753 single base substitution C T intron_variant MELA-AU 9 119460082 119460082 single base substitution C T missense_variant P21S 61C>T MELA-AU 9 119461653 119461653 single base substitution C T downstream_gene_variant MELA-AU 9 119461653 119461653 single base substitution C T synonymous_variant H544H 1632C>T MELA-AU 9 119461829 119461829 single base substitution C T downstream_gene_variant MELA-AU 9 119461829 119461829 single base substitution C T missense_variant P603L 1808C>T MELA-AU 9 119461853 119461853 single base substitution T G downstream_gene_variant MELA-AU 9 119461853 119461853 single base substitution T G missense_variant L611R 1832T>G MELA-AU 9 119461869 119461869 single base substitution T C downstream_gene_variant MELA-AU 9 119461869 119461869 single base substitution T C synonymous_variant L616L 1848T>C MELA-AU 9 119462014 119462014 single base substitution C T 3_prime_UTR_variant MELA-AU 9 119462014 119462014 single base substitution C T downstream_gene_variant MELA-AU 9 119462082 119462082 single base substitution C T 3_prime_UTR_variant MELA-AU 9 119462082 119462082 single base substitution C T downstream_gene_variant MELA-AU 9 119463068 119463068 single base substitution T C 3_prime_UTR_variant MELA-AU 9 119463068 119463068 single base substitution T C downstream_gene_variant MELA-AU 9 119463233 119463234 multiple base substitution (>=2bp and <=200bp) CC TT 3_prime_UTR_variant MELA-AU 9 119463233 119463234 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 9 119463496 119463496 single base substitution T A 3_prime_UTR_variant MELA-AU 9 119463496 119463496 single base substitution T A downstream_gene_variant MELA-AU 9 119463705 119463705 single base substitution T C downstream_gene_variant MELA-AU 9 119464527 119464527 single base substitution C T downstream_gene_variant MELA-AU 9 119465035 119465035 single base substitution C T downstream_gene_variant MELA-AU 9 119466619 119466619 single base substitution A T downstream_gene_variant MELA-AU 9 119466883 119466883 single base substitution T C downstream_gene_variant MELA-AU 9 119468069 119468069 single base substitution G A downstream_gene_variant MELA-AU 9 119468432 119468432 single base substitution C G downstream_gene_variant MELA-AU 9 119468436 119468436 single base substitution C T downstream_gene_variant ORCA-IN 9 119453251 119453251 single base substitution T C intron_variant OV-AU 9 119447716 119447716 single base substitution C T upstream_gene_variant OV-AU 9 119451180 119451180 single base substitution G T intron_variant OV-AU 9 119461677 119461677 single base substitution T C downstream_gene_variant OV-AU 9 119461677 119461677 single base substitution T C synonymous_variant I552I 1656T>C PACA-AU 9 119446120 119446120 single base substitution C G upstream_gene_variant PACA-AU 9 119447062 119447062 single base substitution A C upstream_gene_variant PACA-AU 9 119455661 119455661 single base substitution T A intron_variant PACA-AU 9 119460003 119460003 single base substitution A T 5_prime_UTR_variant PACA-AU 9 119460629 119460629 single base substitution G A downstream_gene_variant PACA-AU 9 119460629 119460629 single base substitution G A missense_variant R203Q 608G>A PACA-AU 9 119462024 119462024 single base substitution T C 3_prime_UTR_variant PACA-AU 9 119462024 119462024 single base substitution T C downstream_gene_variant PACA-AU 9 119462644 119462644 single base substitution G A 3_prime_UTR_variant PACA-AU 9 119462644 119462644 single base substitution G A downstream_gene_variant PACA-AU 9 119467091 119467095 deletion of <=200bp TAAAG - downstream_gene_variant PACA-CA 9 119445449 119445449 single base substitution C G upstream_gene_variant PACA-CA 9 119446066 119446066 single base substitution T C upstream_gene_variant PACA-CA 9 119446698 119446698 single base substitution T C upstream_gene_variant PACA-CA 9 119451386 119451386 insertion of <=200bp - C intron_variant PACA-CA 9 119453418 119453418 single base substitution C T intron_variant PACA-CA 9 119453562 119453562 insertion of <=200bp - AG intron_variant PACA-CA 9 119453898 119453898 single base substitution C T intron_variant PACA-CA 9 119460118 119460118 single base substitution C T missense_variant R33C 97C>T PACA-CA 9 119461048 119461063 deletion of <=200bp CAGCGGGGTCCTGAGG - downstream_gene_variant PACA-CA 9 119461048 119461063 deletion of <=200bp CAGCGGGGTCCTGAGG - frameshift_variant QRGPEA343 PACA-CA 9 119461294 119461294 single base substitution G T downstream_gene_variant PACA-CA 9 119461294 119461294 single base substitution G T missense_variant D425Y 1273G>T PACA-CA 9 119461730 119461730 single base substitution C A downstream_gene_variant PACA-CA 9 119461730 119461730 single base substitution C A stop_gained S570* 1709C>A PAEN-AU 9 119465073 119465073 single base substitution G T downstream_gene_variant PAEN-AU 9 119465337 119465337 single base substitution A C downstream_gene_variant PAEN-AU 9 119466879 119466879 single base substitution T C downstream_gene_variant PAEN-IT 9 119448403 119448403 single base substitution C T upstream_gene_variant PAEN-IT 9 119464039 119464039 single base substitution T C downstream_gene_variant PBCA-DE 9 119449746 119449746 single base substitution C T intron_variant PRAD-CA 9 119453973 119453973 single base substitution C G intron_variant PRAD-CA 9 119459346 119459346 single base substitution G A intron_variant PRAD-UK 9 119460635 119460635 single base substitution T A downstream_gene_variant PRAD-UK 9 119460635 119460635 single base substitution T A missense_variant F205Y 614T>A PRAD-UK 9 119466011 119466011 insertion of <=200bp - T downstream_gene_variant RECA-EU 9 119447723 119447723 single base substitution T A upstream_gene_variant RECA-EU 9 119448622 119448622 single base substitution C T upstream_gene_variant SKCA-BR 9 119445846 119445846 single base substitution G A upstream_gene_variant SKCA-BR 9 119448657 119448657 single base substitution A T upstream_gene_variant SKCA-BR 9 119452069 119452069 single base substitution T A intron_variant SKCA-BR 9 119452099 119452099 single base substitution T G intron_variant SKCA-BR 9 119454069 119454069 single base substitution T A intron_variant SKCA-BR 9 119454813 119454813 single base substitution C T intron_variant SKCA-BR 9 119455831 119455831 single base substitution A T intron_variant SKCA-BR 9 119456141 119456141 single base substitution A G intron_variant SKCA-BR 9 119456954 119456954 single base substitution C G intron_variant SKCA-BR 9 119458931 119458931 single base substitution G A intron_variant SKCM-US 9 119460032 119460032 single base substitution C T missense_variant A4V 11C>T SKCM-US 9 119460989 119460989 single base substitution G C downstream_gene_variant SKCM-US 9 119460989 119460989 single base substitution G C missense_variant R323T 968G>C SKCM-US 9 119461105 119461105 single base substitution G A downstream_gene_variant SKCM-US 9 119461105 119461105 single base substitution G A missense_variant G362R 1084G>A SKCM-US 9 119461141 119461141 single base substitution C T downstream_gene_variant SKCM-US 9 119461141 119461141 single base substitution C T missense_variant P374S 1120C>T SKCM-US 9 119461243 119461243 single base substitution C A downstream_gene_variant SKCM-US 9 119461243 119461243 single base substitution C A missense_variant R408S 1222C>A SKCM-US 9 119461313 119461313 single base substitution C T downstream_gene_variant SKCM-US 9 119461313 119461313 single base substitution C T missense_variant P431L 1292C>T SKCM-US 9 119461791 119461791 single base substitution C T downstream_gene_variant SKCM-US 9 119461791 119461791 single base substitution C T synonymous_variant I590I 1770C>T STAD-US 9 119460614 119460614 single base substitution A G downstream_gene_variant STAD-US 9 119460614 119460614 single base substitution A G missense_variant E198G 593A>G STAD-US 9 119460783 119460783 single base substitution G A downstream_gene_variant STAD-US 9 119460783 119460783 single base substitution G A synonymous_variant L254L 762G>A STAD-US 9 119461051 119461051 single base substitution C T downstream_gene_variant STAD-US 9 119461051 119461051 single base substitution C T missense_variant R344W 1030C>T STAD-US 9 119461292 119461292 single base substitution C T downstream_gene_variant STAD-US 9 119461292 119461292 single base substitution C T missense_variant A424V 1271C>T STAD-US 9 119461306 119461306 single base substitution C A downstream_gene_variant STAD-US 9 119461306 119461306 single base substitution C A missense_variant L429I 1285C>A STAD-US 9 119461528 119461528 deletion of <=200bp G - downstream_gene_variant STAD-US 9 119461528 119461528 deletion of <=200bp G - frameshift_variant G503 STAD-US 9 119461547 119461547 single base substitution G A downstream_gene_variant STAD-US 9 119461547 119461547 single base substitution G A missense_variant C509Y 1526G>A STAD-US 9 119461675 119461675 single base substitution A T downstream_gene_variant STAD-US 9 119461675 119461675 single base substitution A T missense_variant I552F 1654A>T THCA-SA 9 119449609 119449609 single base substitution G C 5_prime_UTR_variant THCA-SA 9 119449609 119449609 single base substitution G C upstream_gene_variant THCA-SA 9 119463189 119463189 single base substitution T C 3_prime_UTR_variant THCA-SA 9 119463189 119463189 single base substitution T C downstream_gene_variant THCA-US 9 119460294 119460294 single base substitution C T synonymous_variant L91L 273C>T UCEC-US 9 119460073 119460073 single base substitution C A missense_variant L18I 52C>A UCEC-US 9 119460118 119460118 single base substitution C T missense_variant R33C 97C>T UCEC-US 9 119460168 119460168 single base substitution G A synonymous_variant E49E 147G>A UCEC-US 9 119460193 119460193 single base substitution G T missense_variant G58C 172G>T UCEC-US 9 119460226 119460226 single base substitution C T missense_variant R69C 205C>T UCEC-US 9 119460227 119460227 single base substitution G A missense_variant R69H 206G>A UCEC-US 9 119460232 119460232 single base substitution A G missense_variant T71A 211A>G UCEC-US 9 119460400 119460400 single base substitution G A missense_variant D127N 379G>A UCEC-US 9 119460539 119460539 single base substitution T C missense_variant V173A 518T>C UCEC-US 9 119460539 119460539 single base substitution T C synonymous_variant ?173 UCEC-US 9 119460597 119460597 single base substitution G A downstream_gene_variant UCEC-US 9 119460597 119460597 single base substitution G A synonymous_variant E192E 576G>A UCEC-US 9 119460626 119460626 single base substitution C T downstream_gene_variant UCEC-US 9 119460626 119460626 single base substitution C T missense_variant S202F 605C>T UCEC-US 9 119460636 119460636 single base substitution C A downstream_gene_variant UCEC-US 9 119460636 119460636 single base substitution C A missense_variant F205L 615C>A UCEC-US 9 119460897 119460897 single base substitution A G downstream_gene_variant UCEC-US 9 119460897 119460897 single base substitution A G synonymous_variant G292G 876A>G UCEC-US 9 119461052 119461052 single base substitution G A downstream_gene_variant UCEC-US 9 119461052 119461052 single base substitution G A missense_variant R344Q 1031G>A UCEC-US 9 119461093 119461093 single base substitution C A downstream_gene_variant UCEC-US 9 119461093 119461093 single base substitution C A missense_variant L358I 1072C>A UCEC-US 9 119461766 119461766 single base substitution G A downstream_gene_variant UCEC-US 9 119461766 119461766 single base substitution G A missense_variant C582Y 1745G>A UCEC-US 9 119461819 119461819 single base substitution C A downstream_gene_variant UCEC-US 9 119461819 119461819 single base substitution C A missense_variant L600I 1798C>A UCEC-US 9 119461829 119461829 single base substitution C A downstream_gene_variant UCEC-US 9 119461829 119461829 single base substitution C A missense_variant P603H 1808C>A

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-CU-A3YL-01 COSM3779589 c.1853G>A p.C618Y Substitution - Missense 9:116699595-116699595 + TCGA-HU-8610-01 COSM3903534 c.1654A>T p.I552F Substitution - Missense 9:116699396-116699396 + BK0006 COSM4185593 c.721T>C p.Y241H Substitution - Missense 9:116698463-116698463 + CSCC-6-T COSM4549320 c.46G>A p.E16K Substitution - Missense 9:116697788-116697788 + S00539 COSM5658929 c.859G>T p.G287C Substitution - Missense 9:116698601-116698601 + TCGA-B5-A0JY-01 COSM1104560 c.1798C>A p.L600I Substitution - Missense 9:116699540-116699540 + TCGA-D1-A167-01 COSM1104534 c.172G>T p.G58C Substitution - Missense 9:116697914-116697914 + 255 COSM3731771 c.1632C>T p.H544H Substitution - coding silent 9:116699374-116699374 + TCGA-66-2759-01 COSM751881 c.812G>A p.R271Q Substitution - Missense 9:116698554-116698554 + TCGA-Q1-A6DT-01 COSM4850869 c.672G>C p.Q224H Substitution - Missense 9:116698414-116698414 + B80 COSM1757243 c.1129C>T p.L377F Substitution - Missense 9:116698871-116698871 + 139 COSM3723970 c.99T>C p.R33R Substitution - coding silent 9:116697841-116697841 + TCGA-GV-A3JZ-01 COSM1314402 c.1323G>A p.L441L Substitution - coding silent 9:116699065-116699065 + PT40 COSM5210384 c.1856C>T p.P619L Substitution - Missense 9:116699598-116699598 + HCC172T COSM3664043 c.1924A>G p.I642V Substitution - Missense 9:116699666-116699666 + ESCC_143 COSM5644493 c.494G>T p.R165L Substitution - Missense 9:116698236-116698236 + 2T COSM3733696 c.1243G>T p.D415Y Substitution - Missense 9:116698985-116698985 + 587344 COSM1230314 c.1735G>C p.A579P Substitution - Missense 9:116699477-116699477 + PD11340a COSM5772883 c.807G>A p.L269L Substitution - coding silent 9:116698549-116698549 + TCGA-G4-6628-01 COSM1459632 c.1961_1962insT p.*654fs? Insertion - Frameshift 9:116699703-116699704 + PCSI_0076_Pa_X COSM3382369 c.1709C>A p.S570* Substitution - Nonsense 9:116699451-116699451 + 587278 COSM1230315 c.1526G>A p.C509Y Substitution - Missense 9:116699268-116699268 + CHEWS010 COSM4588403 c.1354C>T p.L452F Substitution - Missense 9:116699096-116699096 + PCSI_0083_Pa_P_526 COSM1104530 c.97C>T p.R33C Substitution - Missense 9:116697839-116697839 + TCGA-HU-8602-01 COSM3903530 c.593A>G p.E198G Substitution - Missense 9:116698335-116698335 + TCGA-BR-6458-01 COSM3903532 c.1271C>T p.A424V Substitution - Missense 9:116699013-116699013 + BD114T COSM5503520 c.44G>A p.R15Q Substitution - Missense 9:116697786-116697786 + LUAD_E00565 COSM389716 c.1045G>T p.A349S Substitution - Missense 9:116698787-116698787 + TCGA-AP-A059-01 COSM1104532 c.147G>A p.E49E Substitution - coding silent 9:116697889-116697889 + 16461 COSM5617476 c.897G>A p.R299R Substitution - coding silent 9:116698639-116698639 + T155 COSM1176428 c.553C>A p.L185I Substitution - Missense 9:116698295-116698295 + CSCC-29-T COSM4467594 c.1498C>T p.R500* Substitution - Nonsense 9:116699240-116699240 + BD216T COSM5517928 c.1524_1525insCT p.C509fs*26 Insertion - Frameshift 9:116699266-116699267 + TCGA-B8-4153-01 COSM486979 c.292C>A p.L98I Substitution - Missense 9:116698034-116698034 + 8069463 COSM4406815 c.608G>A p.R203Q Substitution - Missense 9:116698350-116698350 + TCGA-GF-A6C9-06 COSM4902634 c.1120C>T p.P374S Substitution - Missense 9:116698862-116698862 + TCGA-B5-A11U-01 COSM1104538 c.206G>A p.R69H Substitution - Missense 9:116697948-116697948 + TCGA-BR-6452-01 COSM3903531 c.762G>A p.L254L Substitution - coding silent 9:116698504-116698504 + B80-Tumor COSM1757243 c.1129C>T p.L377F Substitution - Missense 9:116698871-116698871 + cSCCP7 COSM139802 c.61C>T p.P21S Substitution - Missense 9:116697803-116697803 + 8031110 COSM1169161 c.1417T>C p.W473R Substitution - Missense 9:116699159-116699159 + 2P3 COSM3733696 c.1243G>T p.D415Y Substitution - Missense 9:116698985-116698985 + T3059 COSM4736034 c.464G>A p.R155H Substitution - Missense 9:116698206-116698206 + TCGA-BS-A0TA-01 COSM1104536 c.205C>T p.R69C Substitution - Missense 9:116697947-116697947 + TCGA-AP-A051-01 COSM1104542 c.379G>A p.D127N Substitution - Missense 9:116698121-116698121 + TCGA-46-3765-01 COSM751879 c.1397G>T p.R466M Substitution - Missense 9:116699139-116699139 + TCGA-E1-5307-01 COSM3929773 c.1223G>A p.R408H Substitution - Missense 9:116698965-116698965 + 63 COSM4549320 c.46G>A p.E16K Substitution - Missense 9:116697788-116697788 + CSCC-29-T COSM4513006 c.923C>T p.A308V Substitution - Missense 9:116698665-116698665 + PM-2 COSM5619588 c.511G>T p.E171* Substitution - Nonsense 9:116698253-116698253 + CSCC-31-T COSM4538301 c.252G>A p.K84K Substitution - coding silent 9:116697994-116697994 + TCGA-DK-A1AB-01 COSM421977 c.302G>A p.R101Q Substitution - Missense 9:116698044-116698044 + PD4137a COSM165130 c.1926C>T p.I642I Substitution - coding silent 9:116699668-116699668 + P51 COSM328709 c.499A>T p.K167* Substitution - Nonsense 9:116698241-116698241 + T1240 COSM4736036 c.1161C>T p.V387V Substitution - coding silent 9:116698903-116698903 + TCGA-29-1769-01 COSM1330772 c.714C>T p.R238R Substitution - coding silent 9:116698456-116698456 + NB07C COSM1236540 c.972G>T p.E324D Substitution - Missense 9:116698714-116698714 + SJDES016 COSM4588402 c.938C>T p.A313V Substitution - Missense 9:116698680-116698680 + SNU-C4 COSM4654420 c.1606A>G p.N536D Substitution - Missense 9:116699348-116699348 + DLD1 COSM3321949 c.1088C>T p.A363V Substitution - Missense 9:116698830-116698830 + pfg008T COSM1643718 c.12A>C p.A4A Substitution - coding silent 9:116697754-116697754 + T3202 COSM4736033 c.244G>A p.V82M Substitution - Missense 9:116697986-116697986 + HCT15 COSM3321949 c.1088C>T p.A363V Substitution - Missense 9:116698830-116698830 + TCGA-CK-5916-01 COSM3653561 c.1770C>T p.I590I Substitution - coding silent 9:116699512-116699512 + TCGA-34-2600-01 COSM751882 c.277G>T p.E93* Substitution - Nonsense 9:116698019-116698019 + TCGA-CH-5769-01 COSM1132610 c.1030C>T p.R344W Substitution - Missense 9:116698772-116698772 + ESCC_72 COSM5634424 c.1094G>T p.G365V Substitution - Missense 9:116698836-116698836 + ESO-0280 COSM1268529 c.1384G>A p.V462M Substitution - Missense 9:116699126-116699126 + GC_370T-GC_370N COSM4773108 c.284T>G p.V95G Substitution - Missense 9:116698026-116698026 + TCGA-D1-A17A-01 COSM1104554 c.1031G>A p.R344Q Substitution - Missense 9:116698773-116698773 + 6115251 COSM1104538 c.206G>A p.R69H Substitution - Missense 9:116697948-116697948 + PCSI_0122_Pa_X COSM3382407 c.1273G>T p.D425Y Substitution - Missense 9:116699015-116699015 + HCT8 COSM3321949 c.1088C>T p.A363V Substitution - Missense 9:116698830-116698830 + cSCCP7 COSM139803 c.666G>T p.E222D Substitution - Missense 9:116698408-116698408 + TCGA-EW-A1OZ-01 COSM1489616 c.234C>G p.D78E Substitution - Missense 9:116697976-116697976 + STC263 COSM5063563 c.1415C>A p.P472Q Substitution - Missense 9:116699157-116699157 + TCGA-DJ-A1QH-01 COSM3375050 c.273C>T p.L91L Substitution - coding silent 9:116698015-116698015 + 587336 COSM1230317 c.797C>T p.T266I Substitution - Missense 9:116698539-116698539 + TCGA-AX-A0J0-01 COSM1104550 c.615C>A p.F205L Substitution - Missense 9:116698357-116698357 + PD2175a COSM27617 c.1640A>C p.E547A Substitution - Missense 9:116699382-116699382 + LS411 COSM3321925 c.112C>A p.H38N Substitution - Missense 9:116697854-116697854 + HCC172 COSM3664043 c.1924A>G p.I642V Substitution - Missense 9:116699666-116699666 + TCGA-D3-A2JN-06 COSM3653561 c.1770C>T p.I590I Substitution - coding silent 9:116699512-116699512 + TCGA-AP-A051-01 COSM1104558 c.1745G>A p.C582Y Substitution - Missense 9:116699487-116699487 + 2318503 COSM4777424 c.1291C>A p.P431T Substitution - Missense 9:116699033-116699033 + TCGA-EE-A29E-06 COSM3653558 c.11C>T p.A4V Substitution - Missense 9:116697753-116697753 + AOCS-064-3-3 COSM4152007 c.1656T>C p.I552I Substitution - coding silent 9:116699398-116699398 + TCGA-BH-A0HA-01 COSM455245 c.556C>T p.Q186* Substitution - Nonsense 9:116698298-116698298 + CCRF-CEM COSM751881 c.812G>A p.R271Q Substitution - Missense 9:116698554-116698554 + TCGA-CD-8536-01 COSM1230315 c.1526G>A p.C509Y Substitution - Missense 9:116699268-116699268 + Pat_41_B COSM5875432 c.20C>T p.S7F Substitution - Missense 9:116697762-116697762 + TCGA-EE-A2GR-06 COSM3653560 c.1292C>T p.P431L Substitution - Missense 9:116699034-116699034 + CHEWS031 COSM4588401 c.90G>A p.E30E Substitution - coding silent 9:116697832-116697832 + TCGA-06-0128-01 COSM35597 c.1578C>T p.T526T Substitution - coding silent 9:116699320-116699320 + SJDES016-R COSM4588402 c.938C>T p.A313V Substitution - Missense 9:116698680-116698680 + TCGA-FW-A3R5-06 COSM3926051 c.1222C>A p.R408S Substitution - Missense 9:116698964-116698964 + TCGA-AX-A05W-01 COSM1104548 c.605C>T p.S202F Substitution - Missense 9:116698347-116698347 + TCGA-BG-A0M0-01 COSM1104530 c.97C>T p.R33C Substitution - Missense 9:116697839-116697839 + HCA7 COSM4631346 c.178C>T p.R60C Substitution - Missense 9:116697920-116697920 + 587224 COSM1230313 c.572A>C p.E191A Substitution - Missense 9:116698314-116698314 + TCGA-B5-A11E-01 COSM1104546 c.576G>A p.E192E Substitution - coding silent 9:116698318-116698318 + TCGA-P4-A5EA-01 COSM3996270 c.1610T>A p.L537Q Substitution - Missense 9:116699352-116699352 + LS513 COSM3321963 c.1754C>T p.A585V Substitution - Missense 9:116699496-116699496 + TCGA-AP-A054-01 COSM1104544 c.518T>C p.V173A Substitution - Missense 9:116698260-116698260 + TCGA-AP-A051-01 COSM1104562 c.1808C>A p.P603H Substitution - Missense 9:116699550-116699550 + TCGA-D1-A15X-01 COSM1104540 c.211A>G p.T71A Substitution - Missense 9:116697953-116697953 + 0061_CRUK_PC_0061_T1_DNA COSM5423932 c.614T>A p.F205Y Substitution - Missense 9:116698356-116698356 + TCGA-BR-4280-01 COSM3903533 c.1285C>A p.L429I Substitution - Missense 9:116699027-116699027 + TCGA-AP-A051-01 COSM1104552 c.876A>G p.G292G Substitution - coding silent 9:116698618-116698618 + T3498 COSM1104552 c.876A>G p.G292G Substitution - coding silent 9:116698618-116698618 + 1N65-VS-1T65 COSM4978167 c.738C>G p.I246M Substitution - Missense 9:116698480-116698480 + TCGA-33-4532-01 COSM751878 c.1816G>T p.G606W Substitution - Missense 9:116699558-116699558 + DU-145 COSM1674753 c.1537G>T p.A513S Substitution - Missense 9:116699279-116699279 + Pat_24_B COSM5875433 c.1162G>A p.A388T Substitution - Missense 9:116698904-116698904 + SNUH_G10_S1 COSM3321943 c.660G>C p.V220V Substitution - coding silent 9:116698402-116698402 + YUKAT COSM5410267 c.1465G>A p.E489K Substitution - Missense 9:116699207-116699207 + TCGA-AA-3715-01 COSM270392 c.395G>A p.G132D Substitution - Missense 9:116698137-116698137 + sysucc-1397T COSM1104530 c.97C>T p.R33C Substitution - Missense 9:116697839-116697839 + PD14453a COSM5777214 c.1278A>T p.L426L Substitution - coding silent 9:116699020-116699020 + TCGA-GF-A6C9-06 COSM4901530 c.1084G>A p.G362R Substitution - Missense 9:116698826-116698826 + TCGA-06-0128 COSM35597 c.1578C>T p.T526T Substitution - coding silent 9:116699320-116699320 + 54 COSM5734929 c.1756C>T p.R586C Substitution - Missense 9:116699498-116699498 + PTC-7C COSM4163278 c.574G>A p.E192K Substitution - Missense 9:116698316-116698316 + LUAD-NYU1219 COSM370311 c.1677G>T p.G559G Substitution - coding silent 9:116699419-116699419 + TCGA-AR-A254-01 COSM1489617 c.551T>A p.V184D Substitution - Missense 9:116698293-116698293 + TCGA-BR-4362-01 COSM1132610 c.1030C>T p.R344W Substitution - Missense 9:116698772-116698772 + T3094 COSM4736035 c.1125C>T p.V375V Substitution - coding silent 9:116698867-116698867 + 587278 COSM1230316 c.1787G>A p.R596H Substitution - Missense 9:116699529-116699529 + 575 COSM3723971 c.247C>T p.L83L Substitution - coding silent 9:116697989-116697989 + TCGA-G4-6315-01 COSM1459631 c.1923G>C p.K641N Substitution - Missense 9:116699665-116699665 + TCGA-AM-5820-01 COSM3763583 c.1254G>A p.V418V Substitution - coding silent 9:116698996-116698996 + TCGA-AP-A056-01 COSM1104556 c.1072C>A p.L358I Substitution - Missense 9:116698814-116698814 + TCGA-D1-A103-01 COSM1104528 c.52C>A p.L18I Substitution - Missense 9:116697794-116697794 + TCGA-EE-A3AF-06 COSM3653559 c.968G>C p.R323T Substitution - Missense 9:116698710-116698710 + LUAD-CHTN-3090415 COSM357440 c.327G>C p.R109R Substitution - coding silent 9:116698069-116698069 + 587376 COSM1230318 c.1618C>T p.R540W Substitution - Missense 9:116699360-116699360 + CSCC-6-T COSM4531477 c.1792G>A p.E598K Substitution - Missense 9:116699534-116699534 + TCGA-A3-3373-01 COSM486980 c.960T>C p.V320V Substitution - coding silent 9:116698702-116698702 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.591909;Hs.591910 9q33.1 602290 2485003|CGAP|BC003154|C/T|non-coding||2220|Validated; 2486096|dbSNP|BC003154|A/G|coding|Val418Val|1383|Validated

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer - A Frameshift p.M24Nfs*32 c.70dupA 9 119460091 HNSC C A Missense p.L429I c.1285C>A 9 119461306 STAD C G Missense p.D78E c.234C>G 9 119460255 BRCA C T Missense p.A316V c.947C>T 9 119460968 CM C T Missense p.A424V c.1271C>T 9 119461292 STAD C T Missense p.P431L c.1292C>T 9 119461313 CM C T Missense p.R33C c.97C>T 9 119460118 UCEC C T Missense p.R69C c.205C>T 9 119460226 UCEC C T Missense p.S202F c.605C>T 9 119460626 UCEC G A Missense p.G150E c.449G>A 9 119460470 CM G A Missense p.R101Q c.302G>A 9 119460323 BLCA G A Missense p.R271Q c.812G>A 9 119460833 LUSC G A Missense p.R344Q c.1031G>A 9 119461052 UCEC G A Missense p.R408H c.1223G>A 9 119461244 LGG G A Missense p.R500Q c.1499G>A 9 119461520 STAD G A Missense p.R69H c.206G>A 9 119460227 UCEC G A Missense p.V462M c.1384G>A 9 119461405 ESCA G C Missense p.R323T c.968G>C 9 119460989 CM G T Missense p.D148Y c.442G>T 9 119460463 LUAD G T Missense p.E324D c.972G>T 9 119460993 NB G T Missense p.G383C c.1147G>T 9 119461168 COREAD G T Missense p.G606W c.1816G>T 9 119461837 LUSC G T Missense p.R466M c.1397G>T 9 119461418 LUSC G T Nonsense p.E93* c.277G>T 9 119460298 LUSC T A Missense p.V184D c.551T>A 9 119460572 BRCA T C Missense p.V173A c.518T>C 9 119460539 UCEC