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 14 94420823 94420823 + Silent SNP C C T TCGA-OR-A5JB-01A-11D-A29I-10 TCGA-OR-A5JB-10A-01D-A29L-10 g.chr14:94420823C>T c.174G>A c.(172-174)gcG>gcA p.A58A BLCA 14 94404063 94404063 + Silent SNP G G C TCGA-GV-A3QI-01A-11D-A21Z-08 TCGA-GV-A3QI-10A-01D-A21Z-08 g.chr14:94404063G>C c.1608C>G c.(1606-1608)gcC>gcG p.A536A BLCA 14 94405833 94405833 + Missense_Mutation SNP G G A TCGA-DK-A1A5-01A-11D-A13W-08 TCGA-DK-A1A5-10A-01D-A13W-08 g.chr14:94405833G>A c.1094C>T c.(1093-1095)tCc>tTc p.S365F BLCA 14 94419818 94419818 + Missense_Mutation SNP C C G TCGA-ZF-A9RL-01A-11D-A38G-08 TCGA-ZF-A9RL-10A-01D-A38J-08 g.chr14:94419818C>G c.370G>C c.(370-372)Gag>Cag p.E124Q BRCA 14 94413838 94413838 + Missense_Mutation SNP G G C TCGA-A8-A07R-01A-21W-A050-09 TCGA-A8-A07R-10B-01D-A047-09 g.chr14:94413838G>C c.765C>G c.(763-765)gaC>gaG p.D255E BRCA 14 94417514 94417514 + Silent SNP G G A TCGA-E2-A15J-01A-11D-A12Q-09 TCGA-E2-A15J-10A-01D-A12Q-09 g.chr14:94417514G>A c.567C>T c.(565-567)cgC>cgT p.R189R BRCA 14 94420823 94420823 + Silent SNP C C T TCGA-AN-A0AL-01A-11W-A019-09 TCGA-AN-A0AL-10A-01W-A021-09 g.chr14:94420823C>T c.174G>A c.(172-174)gcG>gcA p.A58A BRCA 14 94423200 94423200 + Missense_Mutation SNP C C G TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr14:94423200C>G c.79G>C c.(79-81)Gag>Cag p.E27Q CESC 14 94405849 94405849 + Missense_Mutation SNP C C T TCGA-EK-A2R8-01A-21D-A18J-09 TCGA-EK-A2R8-10A-01D-A18J-09 g.chr14:94405849C>T c.1078G>A c.(1078-1080)Gaa>Aaa p.E360K CESC 14 94405904 94405904 + Silent SNP C C T TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr14:94405904C>T c.1023G>A c.(1021-1023)ctG>ctA p.L341L CESC 14 94417385 94417385 + Missense_Mutation SNP C C G TCGA-IR-A3LA-01A-11D-A22X-09 TCGA-IR-A3LA-10A-01D-A22X-09 g.chr14:94417385C>G c.696G>C c.(694-696)caG>caC p.Q232H CESC 14 94420704 94420704 + Missense_Mutation SNP G G T TCGA-EA-A6QX-01A-12D-A33O-09 TCGA-EA-A6QX-10B-01D-A33O-09 g.chr14:94420704G>T c.293C>A c.(292-294)gCa>gAa p.A98E CHOL 14 94401066 94401066 + Missense_Mutation SNP A A G TCGA-W5-AA39-01A-11D-A417-09 TCGA-W5-AA39-10A-01D-A41A-09 g.chr14:94401066A>G c.1700T>C c.(1699-1701)cTc>cCc p.L567P COAD 14 94401050 94401050 + Silent SNP C C T TCGA-AA-A01Q-01A-01W-A005-10 TCGA-AA-A01Q-10A-01W-A005-10 g.chr14:94401050C>T c.1716G>A c.(1714-1716)ccG>ccA p.P572P COAD 14 94401096 94401096 + Missense_Mutation SNP C C A TCGA-CK-6751-01A-11D-1835-10 TCGA-CK-6751-10A-01D-1835-10 g.chr14:94401096C>A c.1670G>T c.(1669-1671)cGa>cTa p.R557L COAD 14 94405566 94405566 + Missense_Mutation SNP C C T TCGA-AA-3877-01A-01W-0995-10 TCGA-AA-3877-10A-01W-0995-10 g.chr14:94405566C>T c.1361G>A c.(1360-1362)gGc>gAc p.G454D COAD 14 94405679 94405679 + Silent SNP G G A TCGA-F4-6855-01A-11D-1924-10 TCGA-F4-6855-10A-01D-1924-10 g.chr14:94405679G>A c.1248C>T c.(1246-1248)ggC>ggT p.G416G COAD 14 94405707 94405707 + Missense_Mutation SNP C C T TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr14:94405707C>T c.1220G>A c.(1219-1221)cGc>cAc p.R407H COAD 14 94405752 94405752 + Missense_Mutation SNP T T A TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr14:94405752T>A c.1175A>T c.(1174-1176)gAc>gTc p.D392V COAD 14 94405798 94405798 + Missense_Mutation SNP A A G TCGA-AA-3877-01A-01W-0995-10 TCGA-AA-3877-10A-01W-0995-10 g.chr14:94405798A>G c.1129T>C c.(1129-1131)Tac>Cac p.Y377H COAD 14 94405856 94405857 + Frame_Shift_Del DEL GC GC - TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr14:94405856_94405857delGC c.1070_1071delGC c.(1069-1071)cgcfs p.R357fs COAD 14 94405860 94405860 + Missense_Mutation SNP G G A TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr14:94405860G>A c.1067C>T c.(1066-1068)gCg>gTg p.A356V COAD 14 94413755 94413755 + Missense_Mutation SNP T T C TCGA-AA-A01Q-01A-01W-A005-10 TCGA-AA-A01Q-10A-01W-A005-10 g.chr14:94413755T>C c.848A>G c.(847-849)aAc>aGc p.N283S COAD 14 94417475 94417475 + Silent SNP G G A TCGA-F4-6703-01A-11D-1835-10 TCGA-F4-6703-10A-01D-1835-10 g.chr14:94417475G>A c.606C>T c.(604-606)gaC>gaT p.D202D COAD 14 94419792 94419792 + Silent SNP C C T TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr14:94419792C>T c.396G>A c.(394-396)acG>acA p.T132T COAD 14 94420823 94420823 + Silent SNP C C T TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr14:94420823C>T c.174G>A c.(172-174)gcG>gcA p.A58A COADREAD 14 94401050 94401050 + Silent SNP C C T TCGA-AA-A01Q-01A-01W-A005-10 TCGA-AA-A01Q-10A-01W-A005-10 g.chr14:94401050C>T c.1716G>A c.(1714-1716)ccG>ccA p.P572P COADREAD 14 94401096 94401096 + Missense_Mutation SNP C C A TCGA-CK-6751-01A-11D-1835-10 TCGA-CK-6751-10A-01D-1835-10 g.chr14:94401096C>A c.1670G>T c.(1669-1671)cGa>cTa p.R557L COADREAD 14 94405566 94405566 + Missense_Mutation SNP C C T TCGA-AA-3877-01A-01W-0995-10 TCGA-AA-3877-10A-01W-0995-10 g.chr14:94405566C>T c.1361G>A c.(1360-1362)gGc>gAc p.G454D COADREAD 14 94405679 94405679 + Silent SNP G G A TCGA-F4-6855-01A-11D-1924-10 TCGA-F4-6855-10A-01D-1924-10 g.chr14:94405679G>A c.1248C>T c.(1246-1248)ggC>ggT p.G416G COADREAD 14 94405707 94405707 + Missense_Mutation SNP C C T TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr14:94405707C>T c.1220G>A c.(1219-1221)cGc>cAc p.R407H COADREAD 14 94405752 94405752 + Missense_Mutation SNP T T A TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr14:94405752T>A c.1175A>T c.(1174-1176)gAc>gTc p.D392V COADREAD 14 94405798 94405798 + Missense_Mutation SNP A A G TCGA-AA-3877-01A-01W-0995-10 TCGA-AA-3877-10A-01W-0995-10 g.chr14:94405798A>G c.1129T>C c.(1129-1131)Tac>Cac p.Y377H COADREAD 14 94405856 94405857 + Frame_Shift_Del DEL GC GC - TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr14:94405856_94405857delGC c.1070_1071delGC c.(1069-1071)cgcfs p.R357fs COADREAD 14 94405860 94405860 + Missense_Mutation SNP G G A TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr14:94405860G>A c.1067C>T c.(1066-1068)gCg>gTg p.A356V COADREAD 14 94413755 94413755 + Missense_Mutation SNP T T C TCGA-AA-A01Q-01A-01W-A005-10 TCGA-AA-A01Q-10A-01W-A005-10 g.chr14:94413755T>C c.848A>G c.(847-849)aAc>aGc p.N283S COADREAD 14 94417349 94417349 + Silent SNP C C T TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr14:94417349C>T c.732G>A c.(730-732)aaG>aaA p.K244K COADREAD 14 94417475 94417475 + Silent SNP G G A TCGA-F4-6703-01A-11D-1835-10 TCGA-F4-6703-10A-01D-1835-10 g.chr14:94417475G>A c.606C>T c.(604-606)gaC>gaT p.D202D COADREAD 14 94419792 94419792 + Silent SNP C C T TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr14:94419792C>T c.396G>A c.(394-396)acG>acA p.T132T COADREAD 14 94420823 94420823 + Silent SNP C C T TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr14:94420823C>T c.174G>A c.(172-174)gcG>gcA p.A58A COADREAD 14 94420823 94420823 + Silent SNP C C T TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr14:94420823C>T c.174G>A c.(172-174)gcG>gcA p.A58A DLBC 14 94405616 94405616 + Silent SNP G G A TCGA-G8-6325-01A-11D-2210-10 TCGA-G8-6325-10A-01D-2210-10 g.chr14:94405616G>A c.1311C>T c.(1309-1311)gcC>gcT p.A437A DLBC 14 94417531 94417531 + Missense_Mutation SNP T T C TCGA-G8-6326-01A-11D-2210-10 TCGA-G8-6326-10A-01D-2210-10 g.chr14:94417531T>C c.550A>G c.(550-552)Aac>Gac p.N184D DLBC 14 94417531 94417531 + Missense_Mutation SNP T T C TCGA-G8-6907-01A-11D-2210-10 TCGA-G8-6907-14A-01D-2210-10 g.chr14:94417531T>C c.550A>G c.(550-552)Aac>Gac p.N184D ESCA 14 94401050 94401050 + Silent SNP C C T TCGA-LN-A49X-01A-31D-A27G-09 TCGA-LN-A49X-10A-01D-A27G-09 g.chr14:94401050C>T c.1716G>A c.(1714-1716)ccG>ccA p.P572P ESCA 14 94404059 94404059 + Missense_Mutation SNP T T C TCGA-L5-A8NQ-01A-11D-A36J-09 TCGA-L5-A8NQ-11A-11D-A36M-09 g.chr14:94404059T>C c.1612A>G c.(1612-1614)Atc>Gtc p.I538V ESCA 14 94405565 94405565 + Silent SNP G G C TCGA-LN-A9FP-01A-31D-A387-09 TCGA-LN-A9FP-10A-01D-A38A-09 g.chr14:94405565G>C c.1362C>G c.(1360-1362)ggC>ggG p.G454G ESCA 14 94413850 94413850 + Silent SNP C C A TCGA-LN-A7HY-01A-12D-A351-09 TCGA-LN-A7HY-10A-01D-A351-09 g.chr14:94413850C>A c.753G>T c.(751-753)acG>acT p.T251T GBM 14 94404157 94404157 + Missense_Mutation SNP G G A TCGA-28-5208-01A-01D-1486-08 TCGA-28-5208-10A-01D-1486-08 g.chr14:94404157G>A c.1514C>T c.(1513-1515)gCg>gTg p.A505V GBM 14 94419793 94419793 + Missense_Mutation SNP G G A TCGA-76-6664-01A-11D-1845-08 TCGA-76-6664-10A-01D-1845-08 g.chr14:94419793G>A c.395C>T c.(394-396)aCg>aTg p.T132M GBMLGG 14 94404157 94404157 + Missense_Mutation SNP G G A TCGA-28-5208-01A-01D-1486-08 TCGA-28-5208-10A-01D-1486-08 g.chr14:94404157G>A c.1514C>T c.(1513-1515)gCg>gTg p.A505V GBMLGG 14 94404157 94404157 + Missense_Mutation SNP G G A TCGA-DU-8167-01A-11D-2253-08 TCGA-DU-8167-10A-01D-2253-08 g.chr14:94404157G>A c.1514C>T c.(1513-1515)gCg>gTg p.A505V GBMLGG 14 94419793 94419793 + Missense_Mutation SNP G G A TCGA-76-6664-01A-11D-1845-08 TCGA-76-6664-10A-01D-1845-08 g.chr14:94419793G>A c.395C>T c.(394-396)aCg>aTg p.T132M HNSC 14 94404063 94404063 + Silent SNP G G C TCGA-BA-A6DE-01A-22D-A31L-08 TCGA-BA-A6DE-10A-01D-A31J-08 g.chr14:94404063G>C c.1608C>G c.(1606-1608)gcC>gcG p.A536A HNSC 14 94404096 94404096 + Silent SNP C C T TCGA-H7-8502-01A-11D-2394-08 TCGA-H7-8502-10A-01D-2394-08 g.chr14:94404096C>T c.1575G>A c.(1573-1575)ctG>ctA p.L525L HNSC 14 94404137 94404137 + Missense_Mutation SNP G G T TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr14:94404137G>T c.1534C>A c.(1534-1536)Ctc>Atc p.L512I HNSC 14 94405553 94405553 + Silent SNP G G A TCGA-CN-A49A-01A-11D-A24D-08 TCGA-CN-A49A-10A-01D-A24F-08 g.chr14:94405553G>A c.1374C>T c.(1372-1374)ttC>ttT p.F458F HNSC 14 94405625 94405625 + Silent SNP G G A TCGA-CN-A49A-01A-11D-A24D-08 TCGA-CN-A49A-10A-01D-A24F-08 g.chr14:94405625G>A c.1302C>T c.(1300-1302)atC>atT p.I434I HNSC 14 94413768 94413768 + Missense_Mutation SNP C C T TCGA-CN-4736-01A-01D-1434-08 TCGA-CN-4736-10A-01D-1434-08 g.chr14:94413768C>T c.835G>A c.(835-837)Ggt>Agt p.G279S HNSC 14 94417390 94417390 + Missense_Mutation SNP C C T TCGA-CQ-A4C9-01A-11D-A25D-08 TCGA-CQ-A4C9-10A-01D-A25E-08 g.chr14:94417390C>T c.691G>A c.(691-693)Gcc>Acc p.A231T HNSC 14 94417436 94417436 + Silent SNP C C T TCGA-CN-6020-01A-11D-1683-08 TCGA-CN-6020-10A-01D-1683-08 g.chr14:94417436C>T c.645G>A c.(643-645)aaG>aaA p.K215K HNSC 14 94417555 94417555 + Missense_Mutation SNP G G C TCGA-CR-7386-01A-11D-2012-08 TCGA-CR-7386-10A-01D-2013-08 g.chr14:94417555G>C c.526C>G c.(526-528)Ctg>Gtg p.L176V HNSC 14 94423168 94423168 + Missense_Mutation SNP C C A TCGA-CV-A45W-01A-11D-A25D-08 TCGA-CV-A45W-10A-01D-A25E-08 g.chr14:94423168C>A c.111G>T c.(109-111)ttG>ttT p.L37F KIPAN 14 94413717 94413717 + Missense_Mutation SNP C C T TCGA-IA-A83V-01A-11D-A34Z-10 TCGA-IA-A83V-11A-11D-A34Z-10 g.chr14:94413717C>T c.886G>A c.(886-888)Gcc>Acc p.A296T KIRP 14 94413717 94413717 + Missense_Mutation SNP C C T TCGA-IA-A83V-01A-11D-A34Z-10 TCGA-IA-A83V-11A-11D-A34Z-10 g.chr14:94413717C>T c.886G>A c.(886-888)Gcc>Acc p.A296T LGG 14 94404157 94404157 + Missense_Mutation SNP G G A TCGA-DU-8167-01A-11D-2253-08 TCGA-DU-8167-10A-01D-2253-08 g.chr14:94404157G>A c.1514C>T c.(1513-1515)gCg>gTg p.A505V LIHC 14 94404109 94404109 + Missense_Mutation SNP A A G TCGA-DD-A3A1-01A-11D-A20W-10 TCGA-DD-A3A1-11A-11D-A20W-10 g.chr14:94404109A>G c.1562T>C c.(1561-1563)cTc>cCc p.L521P LIHC 14 94420805 94420805 + Silent SNP G G A TCGA-DD-AAVZ-01A-11D-A40R-10 TCGA-DD-AAVZ-10A-01D-A40U-10 g.chr14:94420805G>A c.192C>T c.(190-192)gcC>gcT p.A64A LIHC 14 94423206 94423206 + Missense_Mutation SNP G G A TCGA-DD-AADO-01A-11D-A40R-10 TCGA-DD-AADO-10A-01D-A40U-10 g.chr14:94423206G>A c.73C>T c.(73-75)Cct>Tct p.P25S LUAD 14 94401017 94401017 + Silent SNP G G A TCGA-55-8508-01A-11D-2393-08 TCGA-55-8508-10A-01D-2393-08 g.chr14:94401017G>A c.1749C>T c.(1747-1749)taC>taT p.Y583Y LUAD 14 94401024 94401024 + Missense_Mutation SNP A A T TCGA-78-7155-01A-11D-2036-08 TCGA-78-7155-10A-01D-2036-08 g.chr14:94401024A>T c.1742T>A c.(1741-1743)cTg>cAg p.L581Q LUAD 14 94401096 94401096 + Missense_Mutation SNP C C T TCGA-17-Z057-01A-01W-0747-08 TCGA-17-Z057-11A-01W-0747-08 g.chr14:94401096C>T c.1670G>A c.(1669-1671)cGa>cAa p.R557Q LUAD 14 94404047 94404047 + Missense_Mutation SNP C C A TCGA-91-A4BC-01A-11D-A24D-08 TCGA-91-A4BC-10A-01D-A24F-08 g.chr14:94404047C>A c.1624G>T c.(1624-1626)Gca>Tca p.A542S LUAD 14 94404126 94404126 + Silent SNP G G A TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chr14:94404126G>A c.1545C>T c.(1543-1545)taC>taT p.Y515Y LUAD 14 94405652 94405652 + Silent SNP C C T TCGA-86-A4JF-01A-11D-A24P-08 TCGA-86-A4JF-10A-01D-A24P-08 g.chr14:94405652C>T c.1275G>A c.(1273-1275)acG>acA p.T425T LUAD 14 94405662 94405662 + Missense_Mutation SNP T T C TCGA-78-7540-01A-11D-2063-08 TCGA-78-7540-11A-01D-2063-08 g.chr14:94405662T>C c.1265A>G c.(1264-1266)tAt>tGt p.Y422C LUAD 14 94413696 94413696 + Splice_Site SNP T T C TCGA-50-7109-01A-11D-2036-08 TCGA-50-7109-11A-01D-2036-08 g.chr14:94413696T>C c.907A>G c.(907-909)Agg>Ggg p.R303G LUAD 14 94413798 94413798 + Missense_Mutation SNP C C G TCGA-50-5935-01A-11D-1753-08 TCGA-50-5935-11A-01D-1753-08 g.chr14:94413798C>G c.805G>C c.(805-807)Gag>Cag p.E269Q LUAD 14 94417371 94417371 + Missense_Mutation SNP T T G TCGA-55-8507-01A-11D-2393-08 TCGA-55-8507-10A-01D-2393-08 g.chr14:94417371T>G c.710A>C c.(709-711)gAg>gCg p.E237A LUAD 14 94417386 94417386 + Missense_Mutation SNP T T C TCGA-55-7914-01A-11D-2167-08 TCGA-55-7914-10A-01D-2167-08 g.chr14:94417386T>C c.695A>G c.(694-696)cAg>cGg p.Q232R LUAD 14 94417427 94417427 + Silent SNP G G T TCGA-93-A4JN-01A-11D-A24P-08 TCGA-93-A4JN-10A-01D-A24P-08 g.chr14:94417427G>T c.654C>A c.(652-654)tcC>tcA p.S218S LUAD 14 94417428 94417428 + Missense_Mutation SNP G G T TCGA-93-A4JN-01A-11D-A24P-08 TCGA-93-A4JN-10A-01D-A24P-08 g.chr14:94417428G>T c.653C>A c.(652-654)tCc>tAc p.S218Y LUAD 14 94417512 94417512 + Missense_Mutation SNP C C G TCGA-86-8672-01A-21D-2393-08 TCGA-86-8672-10A-01D-2393-08 g.chr14:94417512C>G c.569G>C c.(568-570)gGc>gCc p.G190A LUAD 14 94417524 94417524 + Missense_Mutation SNP C C T TCGA-62-A46P-01A-11D-A24D-08 TCGA-62-A46P-10A-01D-A24F-08 g.chr14:94417524C>T c.557G>A c.(556-558)cGc>cAc p.R186H LUAD 14 94420759 94420759 + Missense_Mutation SNP C C A TCGA-17-Z026-01A-01W-0746-08 TCGA-17-Z026-11A-01W-0746-08 g.chr14:94420759C>A c.238G>T c.(238-240)Ggg>Tgg p.G80W LUAD 14 94420762 94420762 + Missense_Mutation SNP C C T TCGA-17-Z055-01A-01W-0747-08 TCGA-17-Z055-11A-01W-0747-08 g.chr14:94420762C>T c.235G>A c.(235-237)Gaa>Aaa p.E79K LUSC 14 94419793 94419793 + Missense_Mutation SNP G G C TCGA-18-3416-01A-01D-0983-08 TCGA-18-3416-11A-01D-0983-08 g.chr14:94419793G>C c.395C>G c.(394-396)aCg>aGg p.T132R LUSC 14 94420705 94420705 + Missense_Mutation SNP C C A TCGA-22-5489-01A-01D-1632-08 TCGA-22-5489-11A-01D-1632-08 g.chr14:94420705C>A c.292G>T c.(292-294)Gca>Tca p.A98S LUSC 14 94420769 94420769 + Missense_Mutation SNP C C A TCGA-66-2791-01A-01D-0983-08 TCGA-66-2791-11A-01D-0983-08 g.chr14:94420769C>A c.228G>T c.(226-228)atG>atT p.M76I OV 14 94413738 94413738 + Missense_Mutation SNP C C T TCGA-23-2647-01A-01D-1526-09 TCGA-23-2647-10A-01D-1526-09 g.chr14:94413738C>T c.865G>A c.(865-867)Ggc>Agc p.G289S PAAD 14 94417346 94417346 + Splice_Site SNP G G A TCGA-HZ-A77O-01A-11D-A33T-08 TCGA-HZ-A77O-10A-01D-A33W-08 g.chr14:94417346G>A c.735C>T c.(733-735)taC>taT p.Y245Y PAAD 14 94417504 94417504 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr14:94417504C>T c.577G>A c.(577-579)Gct>Act p.A193T PAAD 14 94417571 94417571 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr14:94417571C>T c.510G>A c.(508-510)gcG>gcA p.A170A PAAD 14 94419708 94419708 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr14:94419708C>T c.480G>A c.(478-480)ccG>ccA p.P160P PRAD 14 94401108 94401108 + Missense_Mutation SNP C C T TCGA-CH-5738-01A-11D-1576-08 TCGA-CH-5738-10A-01D-1576-08 g.chr14:94401108C>T c.1658G>A c.(1657-1659)cGa>cAa p.R553Q PRAD 14 94420665 94420665 + Missense_Mutation SNP C C T TCGA-CH-5790-01A-11D-1576-08 TCGA-CH-5790-10A-01D-1576-08 g.chr14:94420665C>T c.332G>A c.(331-333)cGa>cAa p.R111Q PRAD 14 94420793 94420793 + Silent SNP G G A TCGA-2A-A8VO-01A-11D-A377-08 TCGA-2A-A8VO-10A-01D-A37A-08 g.chr14:94420793G>A c.204C>T c.(202-204)ggC>ggT p.G68G READ 14 94417349 94417349 + Silent SNP C C T TCGA-AG-3892-01A-01W-1073-09 TCGA-AG-3892-10A-01W-1073-09 g.chr14:94417349C>T c.732G>A c.(730-732)aaG>aaA p.K244K READ 14 94420823 94420823 + Silent SNP C C T TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr14:94420823C>T c.174G>A c.(172-174)gcG>gcA p.A58A SARC 14 94404161 94404161 + Missense_Mutation SNP A A T TCGA-DX-A1KX-01A-22D-A24N-09 TCGA-DX-A1KX-10A-01D-A24N-09 g.chr14:94404161A>T c.1510T>A c.(1510-1512)Tgg>Agg p.W504R SKCM 14 94401016 94401016 + Missense_Mutation SNP C C T TCGA-D3-A3MR-06A-11D-A21A-08 TCGA-D3-A3MR-10A-01D-A21A-08 g.chr14:94401016C>T c.1750G>A c.(1750-1752)Gag>Aag p.E584K SKCM 14 94401096 94401096 + Missense_Mutation SNP C C T TCGA-DA-A1HW-06A-11D-A19A-08 TCGA-DA-A1HW-10A-01D-A19A-08 g.chr14:94401096C>T c.1670G>A c.(1669-1671)cGa>cAa p.R557Q SKCM 14 94404144 94404144 + Silent SNP G G A TCGA-EE-A2GO-06A-11D-A196-08 TCGA-EE-A2GO-10A-01D-A198-08 g.chr14:94404144G>A c.1527C>T c.(1525-1527)atC>atT p.I509I SKCM 14 94405539 94405539 + Missense_Mutation SNP C C T TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr14:94405539C>T c.1388G>A c.(1387-1389)gGc>gAc p.G463D SKCM 14 94413705 94413705 + Missense_Mutation SNP C C T TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr14:94413705C>T c.898G>A c.(898-900)Ggc>Agc p.G300S SKCM 14 94413746 94413746 + Missense_Mutation SNP T T C TCGA-EE-A2GJ-06A-11D-A196-08 TCGA-EE-A2GJ-10A-01D-A198-08 g.chr14:94413746T>C c.857A>G c.(856-858)aAc>aGc p.N286S SKCM 14 94419799 94419799 + Missense_Mutation SNP A A G TCGA-EE-A2MT-06A-11D-A197-08 TCGA-EE-A2MT-10A-01D-A199-08 g.chr14:94419799A>G c.389T>C c.(388-390)tTg>tCg p.L130S SKCM 14 94420665 94420665 + Missense_Mutation SNP C C T TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr14:94420665C>T c.332G>A c.(331-333)cGa>cAa p.R111Q SKCM 14 94420665 94420665 + Missense_Mutation SNP C C T TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr14:94420665C>T c.332G>A c.(331-333)cGa>cAa p.R111Q SKCM 14 94420818 94420818 + Missense_Mutation SNP G G A TCGA-EE-A2MI-06A-11D-A197-08 TCGA-EE-A2MI-10A-01D-A199-08 g.chr14:94420818G>A c.179C>T c.(178-180)cCc>cTc p.P60L

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-AP-A051-01 COSM959095 c.9C>A p.R3R Substitution - coding silent 14:93956924-93956924 - TCGA-D1-A16X-01 COSM959091 c.332G>A p.R111Q Substitution - Missense 14:93954319-93954319 - TCGA-AN-A0AL-01 COSM171636 c.174G>A p.A58A Substitution - coding silent 14:93954477-93954477 - HCC021T COSM5815814 c.125T>A p.M42K Substitution - Missense 14:93956808-93956808 - GB07 COSM1742808 c.1176C>T p.D392D Substitution - coding silent 14:93939405-93939405 - Pat_41_B COSM3499226 c.179C>T p.P60L Substitution - Missense 14:93954472-93954472 - T256 COSM4663649 c.508G>A p.A170T Substitution - Missense 14:93951227-93951227 - T3024 COSM243074 c.1248C>T p.G416G Substitution - coding silent 14:93939333-93939333 - TCGA-DU-8167-01 COSM3401539 c.1514C>T p.A505V Substitution - Missense 14:93937811-93937811 - 1_RESISTANT COSM1718101 c.290C>T p.A97V Substitution - Missense 14:93954361-93954361 - TCGA-BS-A0UF-01 COSM959079 c.1356C>T p.C452C Substitution - coding silent 14:93939225-93939225 - TCGA-28-5208-01 COSM3401539 c.1514C>T p.A505V Substitution - Missense 14:93937811-93937811 - TCGA-EE-A3JD-06 COSM959091 c.332G>A p.R111Q Substitution - Missense 14:93954319-93954319 - LP6008031-DNA_B01 COSM3815583 c.567C>T p.R189R Substitution - coding silent 14:93951168-93951168 - HT115 COSM198492 c.1716G>A p.P572P Substitution - coding silent 14:93934704-93934704 - TCGA-D5-6930-01 COSM1371738 c.1175A>T p.D392V Substitution - Missense 14:93939406-93939406 - 587222 COSM1183732 c.1674G>T p.K558N Substitution - Missense 14:93934746-93934746 - TCGA-CC-5258-01 COSM4933412 c.1158C>T p.G386G Substitution - coding silent 14:93939423-93939423 - 587316 COSM1183730 c.1462A>G p.S488G Substitution - Missense 14:93939119-93939119 - 587316 COSM1183731 c.1205G>A p.R402H Substitution - Missense 14:93939376-93939376 - HCC2998 COSM1678214 c.359G>A p.R120H Substitution - Missense 14:93953483-93953483 - 18 COSM5745235 c.1049C>T p.P350L Substitution - Missense 14:93939532-93939532 - 08-067 COSM305518 c.273G>C p.W91C Substitution - Missense 14:93954378-93954378 - PTC-7C COSM3754191 c.495C>T p.C165C Substitution - coding silent 14:93951240-93951240 - TCGA-EE-A2GJ-06 COSM3499224 c.857A>G p.N286S Substitution - Missense 14:93947400-93947400 - 1_PRE-TREATMENT COSM1718101 c.290C>T p.A97V Substitution - Missense 14:93954361-93954361 - TCGA-JW-A5VL-01 COSM4846933 c.1023G>A p.L341L Substitution - coding silent 14:93939558-93939558 - TCGA-D1-A17Q-01 COSM959093 c.306G>T p.Q102H Substitution - Missense 14:93954345-93954345 - T3118 COSM4663648 c.585C>T p.H195H Substitution - coding silent 14:93951150-93951150 - TCGA-A8-A07R-01 COSM3815582 c.765C>G p.D255E Substitution - Missense 14:93947492-93947492 - T3225 COSM4663643 c.1002C>T p.D334D Substitution - coding silent 14:93939579-93939579 - TCGA-BS-A0UV-01 COSM959081 c.1251G>A p.A417A Substitution - coding silent 14:93939330-93939330 - 8031146 COSM1168800 c.382G>A p.V128I Substitution - Missense 14:93953460-93953460 - TCGA-AP-A0LM-01 COSM959089 c.557G>A p.R186H Substitution - Missense 14:93951178-93951178 - PD4604a COSM5792904 c.1248C>G p.G416G Substitution - coding silent 14:93939333-93939333 - TCGA-BS-A0TJ-01 COSM959083 c.1220G>A p.R407H Substitution - Missense 14:93939361-93939361 - ESCC_BICR_044T COSM5439865 c.468C>A p.S156S Substitution - coding silent 14:93953374-93953374 - LUAD-AEIUF COSM403249 c.1146G>T p.L382L Substitution - coding silent 14:93939435-93939435 - CHC1754T COSM4792694 c.250G>T p.A84S Substitution - Missense 14:93954401-93954401 - LUAD-RT-S01777 COSM381944 c.304C>G p.Q102E Substitution - Missense 14:93954347-93954347 - TCGA-66-2791-01 COSM318799 c.228G>T p.M76I Substitution - Missense 14:93954423-93954423 - I2L-P19Ta-Tumor-Biopsy COSM5362454 c.1293C>T p.P431P Substitution - coding silent 14:93939288-93939288 - TCGA-IR-A3LA-01 COSM88504 c.696G>C p.Q232H Substitution - Missense 14:93951039-93951039 - SNU-175 COSM2252928 c.1275G>A p.T425T Substitution - coding silent 14:93939306-93939306 - 46M COSM5587224 c.1689C>T p.Y563Y Substitution - coding silent 14:93934731-93934731 - C058 COSM5524610 c.777C>T p.A259A Substitution - coding silent 14:93947480-93947480 - TCGA-DA-A1HW-06 COSM1283528 c.1670G>A p.R557Q Substitution - Missense 14:93934750-93934750 - TCGA-AF-6136-01 COSM3749286 c.1056C>G p.A352A Substitution - coding silent 14:93939525-93939525 - TCGA-BF-A3DL-01 COSM4904740 c.1587C>T p.I529I Substitution - coding silent 14:93937738-93937738 - PTC_330 COSM5960001 c.480G>T p.P160P Substitution - coding silent 14:93953362-93953362 - TCGA-CH-5790-01 COSM959091 c.332G>A p.R111Q Substitution - Missense 14:93954319-93954319 - HCC2998 COSM1283528 c.1670G>A p.R557Q Substitution - Missense 14:93934750-93934750 - TCGA-AC-A23H-01 COSM3815584 c.79G>C p.E27Q Substitution - Missense 14:93956854-93956854 - D12 COSM5006885 c.691G>A p.A231T Substitution - Missense 14:93951044-93951044 - CHC891T COSM4953397 c.1001A>G p.D334G Substitution - Missense 14:93939580-93939580 - SA229 COSM212666 c.433C>T p.Q145* Substitution - Nonsense 14:93953409-93953409 - TCGA-AG-3892-01 COSM256352 c.732G>A p.K244K Substitution - coding silent 14:93951003-93951003 - sysucc-311T COSM1183731 c.1205G>A p.R402H Substitution - Missense 14:93939376-93939376 - TCGA-D1-A17U-01 COSM959085 c.1204C>T p.R402C Substitution - Missense 14:93939377-93939377 - TCGA-DK-A1A5-01 COSM416555 c.1094C>T p.S365F Substitution - Missense 14:93939487-93939487 - TCGA-FV-A23B-01 COSM4914155 c.1146G>A p.L382L Substitution - coding silent 14:93939435-93939435 - TCGA-CH-5738-01 COSM1128163 c.1658G>A p.R553Q Substitution - Missense 14:93934762-93934762 - C058 COSM5524609 c.778C>T p.L260F Substitution - Missense 14:93947479-93947479 - PR-3026 COSM243074 c.1248C>T p.G416G Substitution - coding silent 14:93939333-93939333 - T3049 COSM4663641 c.1261G>A p.A421T Substitution - Missense 14:93939320-93939320 - YUKAT COSM5382925 c.1255A>G p.I419V Substitution - Missense 14:93939326-93939326 - 8044091 COSM3386750 c.1279C>T p.P427S Substitution - Missense 14:93939302-93939302 - 134413 COSM318799 c.228G>T p.M76I Substitution - Missense 14:93954423-93954423 - HCC165T COSM3706446 c.507C>T p.N169N Substitution - coding silent 14:93951228-93951228 - TCGA-P4-A5EA-01 COSM3987838 c.1400A>C p.H467P Substitution - Missense 14:93939181-93939181 - ME016T COSM225027 c.590C>T p.S197F Substitution - Missense 14:93951145-93951145 - TCGA-22-5489-01 COSM699818 c.292G>T p.A98S Substitution - Missense 14:93954359-93954359 - TCGA-AA-3697-01 COSM3749286 c.1056C>G p.A352A Substitution - coding silent 14:93939525-93939525 - I2L-P19Tb-Tumor-Organoid COSM5362533 c.577G>A p.A193T Substitution - Missense 14:93951158-93951158 - TCGA-AP-A056-01 COSM198492 c.1716G>A p.P572P Substitution - coding silent 14:93934704-93934704 - SNUH_G10_S1 COSM3754191 c.495C>T p.C165C Substitution - coding silent 14:93951240-93951240 - CHC1192T COSM4803472 c.648G>C p.V216V Substitution - coding silent 14:93951087-93951087 - TCGA-BR-4280-01 COSM4053195 c.840C>T p.A280A Substitution - coding silent 14:93947417-93947417 - SNUH_G10_S1 COSM3999421 c.660C>T p.N220N Substitution - coding silent 14:93951075-93951075 - SNUH_G10_S1 COSM3999422 c.540T>C p.N180N Substitution - coding silent 14:93951195-93951195 - C99 COSM4620345 c.1116C>G p.V372V Substitution - coding silent 14:93939465-93939465 - TCGA-F4-6703-01 COSM1371741 c.606C>T p.D202D Substitution - coding silent 14:93951129-93951129 - TCGA-AD-6889-01 COSM1371739 c.1070_1071delGC p.R357fs*137 Deletion - Frameshift 14:93939510-93939511 - TCGA-HU-A4GQ-01 COSM4053194 c.876G>A p.P292P Substitution - coding silent 14:93947381-93947381 - TCGA-A5-A0VP-01 COSM959087 c.566G>A p.R189H Substitution - Missense 14:93951169-93951169 - TCGA-BR-4184-01 COSM4053196 c.516C>T p.A172A Substitution - coding silent 14:93951219-93951219 - TCGA-F5-6814-01 COSM3420132 c.133T>C p.Y45H Substitution - Missense 14:93956800-93956800 - ZZUFHECRKL-G035T COSM5440334 c.1533C>A p.V511V Substitution - coding silent 14:93937792-93937792 - PET028T COSM5824747 c.95G>A p.R32Q Substitution - Missense 14:93956838-93956838 - LC_C35 COSM1188898 c.689C>A p.A230D Substitution - Missense 14:93951046-93951046 - VLTS-4 COSM5702652 c.1676C>A p.A559D Substitution - Missense 14:93934744-93934744 - YUBER COSM1707796 c.646G>A p.V216M Substitution - Missense 14:93951089-93951089 - TCGA-D5-6930-01 COSM959083 c.1220G>A p.R407H Substitution - Missense 14:93939361-93939361 - TCGA-EE-A2MT-06 COSM3499225 c.389T>C p.L130S Substitution - Missense 14:93953453-93953453 - DLD1 COSM2252949 c.633C>T p.S211S Substitution - coding silent 14:93951102-93951102 - T3535 COSM4663645 c.875C>T p.P292L Substitution - Missense 14:93947382-93947382 - RK044_C01 COSM1629442 c.1725C>A p.G575G Substitution - coding silent 14:93934695-93934695 - ESO-157 COSM1245534 c.693C>T p.A231A Substitution - coding silent 14:93951042-93951042 - 1N45-VS-1T45 COSM4975796 c.86C>T p.S29L Substitution - Missense 14:93956847-93956847 - DN14067 COSM5960687 c.1357G>A p.D453N Substitution - Missense 14:93939224-93939224 - CHC1192T COSM4803472 c.648G>C p.V216V Substitution - coding silent 14:93951087-93951087 - 49M COSM5589750 c.96G>A p.R32R Substitution - coding silent 14:93956837-93956837 - TCGA-D9-A6EC-06 COSM4404158 c.1388G>A p.G463D Substitution - Missense 14:93939193-93939193 - S01023 COSM5666444 c.424T>C p.S142P Substitution - Missense 14:93953418-93953418 - TCGA-CG-4455-01 COSM4053192 c.1311C>T p.A437A Substitution - coding silent 14:93939270-93939270 - BD114T COSM5504074 c.1332C>T p.L444L Substitution - coding silent 14:93939249-93939249 - ESO-045 COSM959089 c.557G>A p.R186H Substitution - Missense 14:93951178-93951178 - SNU-C2B COSM4651209 c.1172G>A p.R391H Substitution - Missense 14:93939409-93939409 - MINO COSM1740074 c.103A>G p.M35V Substitution - Missense 14:93956830-93956830 - CCK81 COSM2252964 c.216C>A p.A72A Substitution - coding silent 14:93954435-93954435 - HCC56 COSM1608086 c.1292C>T p.P431L Substitution - Missense 14:93939289-93939289 - TCGA-GV-A3QI-01 COSM1300922 c.1608C>G p.A536A Substitution - coding silent 14:93937717-93937717 - TCGA-EE-A2GO-06 COSM3499223 c.1527C>T p.I509I Substitution - coding silent 14:93937798-93937798 - T3658 COSM4663650 c.339C>T p.Y113Y Substitution - coding silent 14:93953503-93953503 - SC_9093 COSM5568986 c.137G>A p.S46N Substitution - Missense 14:93956796-93956796 - TCGA-BR-8680-01 COSM959081 c.1251G>A p.A417A Substitution - coding silent 14:93939330-93939330 - HCC56T COSM1608086 c.1292C>T p.P431L Substitution - Missense 14:93939289-93939289 - ESCC_50 COSM5630862 c.1243C>T p.H415Y Substitution - Missense 14:93939338-93939338 - TCGA-BR-4184-01 COSM4053193 c.1159G>A p.A387T Substitution - Missense 14:93939422-93939422 - CRC-19T COSM5481215 c.885C>T p.I295I Substitution - coding silent 14:93947372-93947372 - T1180 COSM4663646 c.735C>T p.Y245Y Substitution - coding silent 14:93951000-93951000 - I2L-P19Ta-Tumor-Organoid COSM5362454 c.1293C>T p.P431P Substitution - coding silent 14:93939288-93939288 - TCGA-AA-3662-01 COSM3754191 c.495C>T p.C165C Substitution - coding silent 14:93951240-93951240 - TCGA-BP-4968-01 COSM470372 c.462C>A p.N154K Substitution - Missense 14:93953380-93953380 - TARGET-30-PARDCK COSM1283528 c.1670G>A p.R557Q Substitution - Missense 14:93934750-93934750 - TCGA-AA-3663-01 COSM3754191 c.495C>T p.C165C Substitution - coding silent 14:93951240-93951240 - C0049T COSM4422617 c.1751A>T p.E584V Substitution - Missense 14:93934669-93934669 - 381_T COSM3956317 c.737-5C>T p.? Unknown 14:93947525-93947525 - TCGA-18-3416-01 COSM699819 c.395C>G p.T132R Substitution - Missense 14:93953447-93953447 - LUAD-B00416 COSM330943 c.325C>A p.L109M Substitution - Missense 14:93954326-93954326 - CHC1754T COSM4792694 c.250G>T p.A84S Substitution - Missense 14:93954401-93954401 - CSCC-31-T COSM4526383 c.1247G>T p.G416V Substitution - Missense 14:93939334-93939334 - PT27 COSM3690260 c.94C>T p.R32W Substitution - Missense 14:93956839-93956839 - TCGA-F4-6855-01 COSM243074 c.1248C>T p.G416G Substitution - coding silent 14:93939333-93939333 - YUDEXA COSM1707797 c.338A>G p.Y113C Substitution - Missense 14:93953504-93953504 - TCGA-24-2280-01 COSM117573 c.640G>A p.A214T Substitution - Missense 14:93951095-93951095 - 134427 COSM318800 c.493T>A p.C165S Substitution - Missense 14:93951242-93951242 - TCGA-E2-A15J-01 COSM3815583 c.567C>T p.R189R Substitution - coding silent 14:93951168-93951168 - TCGA-CM-5868-01 COSM3749286 c.1056C>G p.A352A Substitution - coding silent 14:93939525-93939525 - HCC165 COSM3706446 c.507C>T p.N169N Substitution - coding silent 14:93951228-93951228 - TCGA-EE-A2MI-06 COSM3499226 c.179C>T p.P60L Substitution - Missense 14:93954472-93954472 - HCT8 COSM2252949 c.633C>T p.S211S Substitution - coding silent 14:93951102-93951102 - HCT15 COSM2252949 c.633C>T p.S211S Substitution - coding silent 14:93951102-93951102 - LUAD-F00368 COSM341026 c.515C>T p.A172V Substitution - Missense 14:93951220-93951220 - T207 COSM4663652 c.8G>A p.R3H Substitution - Missense 14:93956925-93956925 - CHLA-258 COSM4578075 c.1657C>T p.R553* Substitution - Nonsense 14:93934763-93934763 - ESCC-212T COSM3936677 c.336G>A p.A112A Substitution - coding silent 14:93953506-93953506 - TCGA-BR-6452-01 COSM4053197 c.204C>T p.G68G Substitution - coding silent 14:93954447-93954447 - Pa10X COSM84265 c.1188C>T p.P396P Substitution - coding silent 14:93939393-93939393 - sysucc-1640T COSM5765548 c.1664G>A p.R555Q Substitution - Missense 14:93934756-93934756 - Gp2D COSM198494 c.1129T>C p.Y377H Substitution - Missense 14:93939452-93939452 - I2L-P19Tb-Tumor-Biopsy COSM5362533 c.577G>A p.A193T Substitution - Missense 14:93951158-93951158 - SC_9008 COSM5574138 c.1628-3_1628-2insT p.? Unknown 14:93934794-93934795 - HCC2998 COSM1678214 c.359G>A p.R120H Substitution - Missense 14:93953483-93953483 - TCGA-AM-5821-01 COSM3690260 c.94C>T p.R32W Substitution - Missense 14:93956839-93956839 - 19M COSM5578072 c.854C>T p.T285I Substitution - Missense 14:93947403-93947403 - TCGA-23-2647-01 COSM1323321 c.865G>A p.G289S Substitution - Missense 14:93947392-93947392 - 585208 COSM324759 c.1376C>A p.S459* Substitution - Nonsense 14:93939205-93939205 - TCGA-D3-A3MR-06 COSM3499222 c.1750G>A p.E584K Substitution - Missense 14:93934670-93934670 - T3724 COSM4663642 c.1217T>C p.L406P Substitution - Missense 14:93939364-93939364 - T3301 COSM4663647 c.690C>T p.A230A Substitution - coding silent 14:93951045-93951045 - TCGA-EK-A2R8-01 COSM4822673 c.1078G>A p.E360K Substitution - Missense 14:93939503-93939503 - TCGA-76-6664-01 COSM2252958 c.395C>T p.T132M Substitution - Missense 14:93953447-93953447 - J90_T COSM3956316 c.1553A>T p.N518I Substitution - Missense 14:93937772-93937772 - CHC891T COSM4953397 c.1001A>G p.D334G Substitution - Missense 14:93939580-93939580 - T2417 COSM4663647 c.690C>T p.A230A Substitution - coding silent 14:93951045-93951045 - 587338 COSM1183733 c.449C>T p.P150L Substitution - Missense 14:93953393-93953393 - SC_9100 COSM2252936 c.1084C>T p.R362W Substitution - Missense 14:93939497-93939497 - T3064 COSM4663651 c.292G>A p.A98T Substitution - Missense 14:93954359-93954359 - T2940 COSM4663644 c.964G>A p.V322I Substitution - Missense 14:93939617-93939617 - OCC06PT COSM88504 c.696G>C p.Q232H Substitution - Missense 14:93951039-93951039 - TCGA-A6-6781-01 COSM171636 c.174G>A p.A58A Substitution - coding silent 14:93954477-93954477 - TCGA-EA-A6QX-01 COSM4828708 c.293C>A p.A98E Substitution - Missense 14:93954358-93954358 - 10-P1058 COSM4578076 c.1527C>G p.I509M Substitution - Missense 14:93937798-93937798 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.510327 14q31-q32 605759 2460474|CGAP|BC032354|C/T|non-coding||1981|Validated

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G Missense p.L178S c.533T>C 14 94419799 CM A T IntronicSNV . c.207-103T>A 14 94423319 HC A T Missense p.C213S c.637T>A 14 94417588 SCLC C A Missense p.A146S c.436G>T 14 94420705 LUSC C A Missense p.G128W c.382G>T 14 94420759 LUAD C A Missense p.M124I c.372G>T 14 94420769 LUSC C A Missense p.M124I c.372G>T 14 94420769 SCLC C G Missense p.E317Q c.949G>C 14 94413798 LUAD C G Synonymous p.G554G c.1662G>C 14 94404153 STAD C T Missense p.A262T c.784G>A 14 94417441 OV C T Missense p.E127K c.379G>A 14 94420762 LUAD C T Missense p.E632K c.1894G>A 14 94401016 CM C T Missense p.G327S c.979G>A 14 94413768 HNSC C T Missense p.G348S c.1042G>A 14 94413705 CM C T Missense p.R159Q c.476G>A 14 94420665 CM C T Missense p.R159Q c.476G>A 14 94420665 PRAD C T Missense p.R234H c.701G>A 14 94417524 STAD C T Missense p.R237H c.710G>A 14 94417515 UCEC C T Missense p.R455H c.1364G>A 14 94405707 UCEC C T Missense p.R601Q c.1802G>A 14 94401108 PRAD C T Missense p.R605Q c.1814G>A 14 94401096 CM C T Missense p.R605Q c.1814G>A 14 94401096 LUAD C T Synonymous p.A106A c.318G>A 14 94420823 BRCA C T Synonymous p.K263K c.789G>A 14 94417436 HNSC C T Synonymous p.K313K c.939G>A 14 94413808 CM C T Synonymous p.K346K c.1038G>A 14 94413709 CM C T Synonymous p.P444P c.1332C>T 14 94405739 PAAD G A Missense p.A132V c.395C>T 14 94420746 HNSC G A Missense p.A553V c.1658C>T 14 94404157 GBM G A Missense p.A553V c.1658C>T 14 94404157 LGG G A Missense p.L492F c.1474C>T 14 94405597 CM G A Missense p.P108L c.323C>T 14 94420818 CM G A Missense p.R450C c.1348C>T 14 94405723 UCEC G A Missense p.R612C c.1834C>T 14 94401076 CM G A Missense p.S245F c.734C>T 14 94417491 CM G A Missense p.S413F c.1238C>T 14 94405833 BLCA G A Missense p.T180M c.539C>T 14 94419793 GBM G A Nonsense p.Q193* c.577C>T 14 94419755 BRCA G A Synonymous p.A279A c.837C>T 14 94417388 ESCA G A Synonymous p.A328A c.984C>T 14 94413763 STAD G A Synonymous p.A485A c.1455C>T 14 94405616 STAD G A Synonymous p.I557I c.1671C>T 14 94404144 CM G A Synonymous p.I577I c.1731C>T 14 94404084 CM G A Synonymous p.T240T c.720C>T 14 94417505 CM G C Missense p.L224V c.670C>G 14 94417555 HNSC G C Missense p.T180R c.539C>G 14 94419793 LUSC G C Synonymous p.A584A c.1752C>G 14 94404063 BLCA G T Nonsense p.S507* c.1520C>A 14 94405551 SCLC T C Missense p.N334S c.1001A>G 14 94413746 CM