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 19 5455609 5455609 + Missense_Mutation SNP G G A TCGA-OR-A5JF-01A-11D-A29I-10 TCGA-OR-A5JF-10A-01D-A29L-10 g.chr19:5455609G>A c.107G>A c.(106-108)cGt>cAt p.R36H ACC 19 5456615 5456615 + Silent SNP C C T TCGA-OR-A5LA-01A-11D-A29I-10 TCGA-OR-A5LA-10A-01D-A29L-10 g.chr19:5456615C>T c.1113C>T c.(1111-1113)gaC>gaT p.D371D BLCA 19 5455685 5455685 + Missense_Mutation SNP C C A TCGA-UY-A8OB-01A-12D-A42E-08 TCGA-UY-A8OB-11A-12D-A42H-08 g.chr19:5455685C>A c.183C>A c.(181-183)agC>agA p.S61R BLCA 19 5455804 5455804 + Missense_Mutation SNP G G A TCGA-DK-A3IU-01A-11D-A20D-08 TCGA-DK-A3IU-10A-01D-A20D-08 g.chr19:5455804G>A c.302G>A c.(301-303)cGg>cAg p.R101Q BLCA 19 5456194 5456194 + Missense_Mutation SNP C C T TCGA-K4-A83P-01A-11D-A34U-08 TCGA-K4-A83P-10A-01D-A34X-08 g.chr19:5456194C>T c.692C>T c.(691-693)tCg>tTg p.S231L BLCA 19 5456732 5456732 + Silent SNP G G C TCGA-XF-A9SG-01A-12D-A42E-08 TCGA-XF-A9SG-10A-01D-A42H-08 g.chr19:5456732G>C c.1230G>C c.(1228-1230)acG>acC p.T410T BRCA 19 5455667 5455667 + Silent SNP G G A TCGA-A8-A09N-01A-11W-A019-09 TCGA-A8-A09N-10A-01W-A021-09 g.chr19:5455667G>A c.165G>A c.(163-165)ccG>ccA p.P55P BRCA 19 5455855 5455855 + Missense_Mutation SNP C C T TCGA-A8-A08H-01A-21W-A019-09 TCGA-A8-A08H-10A-01W-A021-09 g.chr19:5455855C>T c.353C>T c.(352-354)gCg>gTg p.A118V BRCA 19 5455986 5455986 + Missense_Mutation SNP C C T TCGA-AO-A128-01A-11D-A10M-09 TCGA-AO-A128-10A-01D-A10M-09 g.chr19:5455986C>T c.484C>T c.(484-486)Cgc>Tgc p.R162C BRCA 19 5456398 5456398 + Missense_Mutation SNP T T A TCGA-D8-A13Z-01A-11D-A10Y-09 TCGA-D8-A13Z-10A-01D-A110-09 g.chr19:5456398T>A c.896T>A c.(895-897)gTc>gAc p.V299D BRCA 19 5456459 5456460 + Frame_Shift_Ins INS - - T TCGA-A8-A07G-01A-11W-A050-09 TCGA-A8-A07G-10A-01W-A055-09 g.chr19:5456459_5456460insT c.957_958insT c.(958-960)gacfs p.D320fs BRCA 19 5456653 5456653 + Missense_Mutation SNP G G C TCGA-AC-A5EH-01A-11D-A28B-09 TCGA-AC-A5EH-10A-01D-A28E-09 g.chr19:5456653G>C c.1151G>C c.(1150-1152)tGg>tCg p.W384S CESC 19 5455848 5455848 + Silent SNP C C T TCGA-EK-A2PG-01A-11D-A18J-09 TCGA-EK-A2PG-10A-01D-A18J-09 g.chr19:5455848C>T c.346C>T c.(346-348)Ctg>Ttg p.L116L CESC 19 5456111 5456111 + Silent SNP G G A TCGA-EA-A3HU-01A-11D-A20U-09 TCGA-EA-A3HU-10B-01D-A20U-09 g.chr19:5456111G>A c.609G>A c.(607-609)ttG>ttA p.L203L CESC 19 5456144 5456144 + Silent SNP G G T TCGA-EK-A2R8-01A-21D-A18J-09 TCGA-EK-A2R8-10A-01D-A18J-09 g.chr19:5456144G>T c.642G>T c.(640-642)gtG>gtT p.V214V CESC 19 5456482 5456482 + Missense_Mutation SNP G G A TCGA-EA-A3HU-01A-11D-A20U-09 TCGA-EA-A3HU-10B-01D-A20U-09 g.chr19:5456482G>A c.980G>A c.(979-981)tGc>tAc p.C327Y COAD 19 5455653 5455653 + Missense_Mutation SNP G G T TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr19:5455653G>T c.151G>T c.(151-153)Gcc>Tcc p.A51S COAD 19 5455699 5455699 + Missense_Mutation SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr19:5455699C>T c.197C>T c.(196-198)gCg>gTg p.A66V COAD 19 5455704 5455704 + Missense_Mutation SNP C C T TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr19:5455704C>T c.202C>T c.(202-204)Cgg>Tgg p.R68W COAD 19 5455796 5455796 + Silent SNP A A G TCGA-CK-4950-01A-01D-1719-10 TCGA-CK-4950-10A-01D-1719-10 g.chr19:5455796A>G c.294A>G c.(292-294)gcA>gcG p.A98A COAD 19 5455880 5455880 + Silent SNP C C T TCGA-DM-A1HA-01A-11D-A152-10 TCGA-DM-A1HA-10A-01D-A152-10 g.chr19:5455880C>T c.378C>T c.(376-378)ccC>ccT p.P126P COAD 19 5456201 5456201 + Silent SNP C C T TCGA-A6-6142-01A-11D-1771-10 TCGA-A6-6142-10A-01D-1771-10 g.chr19:5456201C>T c.699C>T c.(697-699)caC>caT p.H233H COAD 19 5456387 5456387 + Silent SNP G G A TCGA-AA-A02W-01A-01W-A00E-09 TCGA-AA-A02W-10A-01W-A00E-09 g.chr19:5456387G>A c.885G>A c.(883-885)caG>caA p.Q295Q COAD 19 5456550 5456550 + Missense_Mutation SNP G G A TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr19:5456550G>A c.1048G>A c.(1048-1050)Gtg>Atg p.V350M COADREAD 19 5455583 5455583 + Silent SNP G G A TCGA-F5-6465-01A-11D-1733-10 TCGA-F5-6465-10A-01D-1733-10 g.chr19:5455583G>A c.81G>A c.(79-81)gcG>gcA p.A27A COADREAD 19 5455653 5455653 + Missense_Mutation SNP G G T TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr19:5455653G>T c.151G>T c.(151-153)Gcc>Tcc p.A51S COADREAD 19 5455699 5455699 + Missense_Mutation SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr19:5455699C>T c.197C>T c.(196-198)gCg>gTg p.A66V COADREAD 19 5455704 5455704 + Missense_Mutation SNP C C T TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr19:5455704C>T c.202C>T c.(202-204)Cgg>Tgg p.R68W COADREAD 19 5455796 5455796 + Silent SNP A A G TCGA-CK-4950-01A-01D-1719-10 TCGA-CK-4950-10A-01D-1719-10 g.chr19:5455796A>G c.294A>G c.(292-294)gcA>gcG p.A98A COADREAD 19 5455803 5455803 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr19:5455803C>T c.301C>T c.(301-303)Cgg>Tgg p.R101W COADREAD 19 5455880 5455880 + Silent SNP C C T TCGA-DM-A1HA-01A-11D-A152-10 TCGA-DM-A1HA-10A-01D-A152-10 g.chr19:5455880C>T c.378C>T c.(376-378)ccC>ccT p.P126P COADREAD 19 5456201 5456201 + Silent SNP C C T TCGA-A6-6142-01A-11D-1771-10 TCGA-A6-6142-10A-01D-1771-10 g.chr19:5456201C>T c.699C>T c.(697-699)caC>caT p.H233H COADREAD 19 5456387 5456387 + Silent SNP G G A TCGA-AA-A02W-01A-01W-A00E-09 TCGA-AA-A02W-10A-01W-A00E-09 g.chr19:5456387G>A c.885G>A c.(883-885)caG>caA p.Q295Q COADREAD 19 5456550 5456550 + Missense_Mutation SNP G G A TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr19:5456550G>A c.1048G>A c.(1048-1050)Gtg>Atg p.V350M DLBC 19 5455866 5455866 + Missense_Mutation SNP G G A TCGA-RQ-AAAT-01A-11D-A38X-10 TCGA-RQ-AAAT-10A-01D-A38X-10 g.chr19:5455866G>A c.364G>A c.(364-366)Gtc>Atc p.V122I ESCA 19 5455606 5455606 + Missense_Mutation SNP C C T TCGA-L5-A8NW-01A-11D-A37C-09 TCGA-L5-A8NW-11A-11D-A37F-09 g.chr19:5455606C>T c.104C>T c.(103-105)tCg>tTg p.S35L ESCA 19 5455945 5455945 + Missense_Mutation SNP C C T TCGA-L5-A4ON-01A-11D-A27G-09 TCGA-L5-A4ON-11A-21D-A27G-09 g.chr19:5455945C>T c.443C>T c.(442-444)cCg>cTg p.P148L ESCA 19 5455995 5455995 + Missense_Mutation SNP G G A TCGA-L5-A43E-01A-11D-A247-09 TCGA-L5-A43E-10A-01D-A247-09 g.chr19:5455995G>A c.493G>A c.(493-495)Gac>Aac p.D165N ESCA 19 5456047 5456047 + Missense_Mutation SNP C C T TCGA-L5-A893-01A-11D-A36J-09 TCGA-L5-A893-11A-21D-A36M-09 g.chr19:5456047C>T c.545C>T c.(544-546)gCg>gTg p.A182V ESCA 19 5456256 5456256 + Silent SNP C C T TCGA-IG-A97I-01A-11D-A387-09 TCGA-IG-A97I-10A-01D-A38A-09 g.chr19:5456256C>T c.754C>T c.(754-756)Ctg>Ttg p.L252L GBMLGG 19 5456174 5456174 + Silent SNP C C T TCGA-FG-A6IZ-01A-11D-A31L-08 TCGA-FG-A6IZ-10A-01D-A31J-08 g.chr19:5456174C>T c.672C>T c.(670-672)gtC>gtT p.V224V HNSC 19 5455843 5455843 + Missense_Mutation SNP C C T TCGA-CV-5977-01A-11D-1683-08 TCGA-CV-5977-11A-01D-1683-08 g.chr19:5455843C>T c.341C>T c.(340-342)gCg>gTg p.A114V HNSC 19 5455848 5455848 + Missense_Mutation SNP C C G TCGA-CV-7424-01A-11D-2078-08 TCGA-CV-7424-10A-01D-2078-08 g.chr19:5455848C>G c.346C>G c.(346-348)Ctg>Gtg p.L116V HNSC 19 5455922 5455922 + Silent SNP C C T TCGA-CR-7369-01A-11D-2129-08 TCGA-CR-7369-10A-01D-2129-08 g.chr19:5455922C>T c.420C>T c.(418-420)aaC>aaT p.N140N HNSC 19 5455986 5455986 + Missense_Mutation SNP C C T TCGA-CQ-7063-01A-11D-2394-08 TCGA-CQ-7063-10A-01D-2394-08 g.chr19:5455986C>T c.484C>T c.(484-486)Cgc>Tgc p.R162C HNSC 19 5456015 5456015 + Silent SNP G G A TCGA-CN-4723-01A-01D-1434-08 TCGA-CN-4723-10A-01D-1434-08 g.chr19:5456015G>A c.513G>A c.(511-513)aaG>aaA p.K171K HNSC 19 5456148 5456148 + Missense_Mutation SNP G G A TCGA-CV-A45Q-01A-11D-A24D-08 TCGA-CV-A45Q-10A-01D-A24F-08 g.chr19:5456148G>A c.646G>A c.(646-648)Gag>Aag p.E216K HNSC 19 5456154 5456154 + Missense_Mutation SNP G G A TCGA-CR-7373-01A-11D-2012-08 TCGA-CR-7373-10A-01D-2013-08 g.chr19:5456154G>A c.652G>A c.(652-654)Gcc>Acc p.A218T HNSC 19 5456159 5456159 + Silent SNP G G A TCGA-CN-6020-01A-11D-1683-08 TCGA-CN-6020-10A-01D-1683-08 g.chr19:5456159G>A c.657G>A c.(655-657)tcG>tcA p.S219S HNSC 19 5456253 5456253 + Missense_Mutation SNP G G A TCGA-DQ-7591-01A-11D-2078-08 TCGA-DQ-7591-10A-01D-2078-08 g.chr19:5456253G>A c.751G>A c.(751-753)Gtg>Atg p.V251M KICH 19 5455971 5455971 + Missense_Mutation SNP G G T TCGA-KO-8408-01A-11D-2310-10 TCGA-KO-8408-11A-01D-2311-10 g.chr19:5455971G>T c.469G>T c.(469-471)Gcc>Tcc p.A157S KICH 19 5455976 5455976 + Silent SNP C C T TCGA-KM-8438-01A-11D-2310-10 TCGA-KM-8438-10A-01D-2311-10 g.chr19:5455976C>T c.474C>T c.(472-474)atC>atT p.I158I KICH 19 5455978 5455978 + Missense_Mutation SNP T T C TCGA-KO-8408-01A-11D-2310-10 TCGA-KO-8408-11A-01D-2311-10 g.chr19:5455978T>C c.476T>C c.(475-477)gTg>gCg p.V159A KIPAN 19 5455579 5455579 + Missense_Mutation SNP A A G TCGA-B4-5838-01A-11D-1669-08 TCGA-B4-5838-10A-01D-1669-08 g.chr19:5455579A>G c.77A>G c.(76-78)cAc>cGc p.H26R KIPAN 19 5455971 5455971 + Missense_Mutation SNP G G T TCGA-KO-8408-01A-11D-2310-10 TCGA-KO-8408-11A-01D-2311-10 g.chr19:5455971G>T c.469G>T c.(469-471)Gcc>Tcc p.A157S KIPAN 19 5455976 5455976 + Silent SNP C C T TCGA-KM-8438-01A-11D-2310-10 TCGA-KM-8438-10A-01D-2311-10 g.chr19:5455976C>T c.474C>T c.(472-474)atC>atT p.I158I KIPAN 19 5455978 5455978 + Missense_Mutation SNP T T C TCGA-KO-8408-01A-11D-2310-10 TCGA-KO-8408-11A-01D-2311-10 g.chr19:5455978T>C c.476T>C c.(475-477)gTg>gCg p.V159A KIPAN 19 5456739 5456739 + Missense_Mutation SNP G G C TCGA-Y8-A8S0-01A-11D-A36X-10 TCGA-Y8-A8S0-10A-01D-A370-10 g.chr19:5456739G>C c.1237G>C c.(1237-1239)Gag>Cag p.E413Q KIRC 19 5455579 5455579 + Missense_Mutation SNP A A G TCGA-B4-5838-01A-11D-1669-08 TCGA-B4-5838-10A-01D-1669-08 g.chr19:5455579A>G c.77A>G c.(76-78)cAc>cGc p.H26R KIRP 19 5456739 5456739 + Missense_Mutation SNP G G C TCGA-Y8-A8S0-01A-11D-A36X-10 TCGA-Y8-A8S0-10A-01D-A370-10 g.chr19:5456739G>C c.1237G>C c.(1237-1239)Gag>Cag p.E413Q LGG 19 5456174 5456174 + Silent SNP C C T TCGA-FG-A6IZ-01A-11D-A31L-08 TCGA-FG-A6IZ-10A-01D-A31J-08 g.chr19:5456174C>T c.672C>T c.(670-672)gtC>gtT p.V224V LIHC 19 5455751 5455751 + Silent SNP C C T TCGA-CC-A7IH-01A-11D-A33K-10 TCGA-CC-A7IH-10A-01D-A33K-10 g.chr19:5455751C>T c.249C>T c.(247-249)gtC>gtT p.V83V LIHC 19 5456001 5456001 + Missense_Mutation SNP A A T TCGA-UB-A7MB-01A-11D-A33Q-10 TCGA-UB-A7MB-10A-01D-A33Q-10 g.chr19:5456001A>T c.499A>T c.(499-501)Acc>Tcc p.T167S LIHC 19 5456638 5456638 + Missense_Mutation SNP A A T TCGA-DD-AAW2-01A-11D-A40P-10 TCGA-DD-AAW2-10A-01D-A40P-10 g.chr19:5456638A>T c.1136A>T c.(1135-1137)cAc>cTc p.H379L LUAD 19 5455509 5455509 + Missense_Mutation SNP C C T TCGA-17-Z059-01A-01W-0747-08 TCGA-17-Z059-11A-01W-0747-08 g.chr19:5455509C>T c.7C>T c.(7-9)Ctc>Ttc p.L3F LUAD 19 5455572 5455572 + Silent SNP C C T TCGA-78-7159-01A-11D-2036-08 TCGA-78-7159-10A-01D-2036-08 g.chr19:5455572C>T c.70C>T c.(70-72)Ctg>Ttg p.L24L LUAD 19 5455636 5455636 + Missense_Mutation SNP C C A TCGA-69-7979-01A-11D-2184-08 TCGA-69-7979-10A-01D-2184-08 g.chr19:5455636C>A c.134C>A c.(133-135)cCc>cAc p.P45H LUAD 19 5455751 5455751 + Silent SNP C C G TCGA-17-Z043-01A-01W-0746-08 TCGA-17-Z043-11A-01W-0746-08 g.chr19:5455751C>G c.249C>G c.(247-249)gtC>gtG p.V83V LUAD 19 5455761 5455761 + Missense_Mutation SNP C C A TCGA-55-7907-01A-11D-2167-08 TCGA-55-7907-10A-01D-2167-08 g.chr19:5455761C>A c.259C>A c.(259-261)Ctg>Atg p.L87M LUAD 19 5455880 5455880 + Silent SNP C C A TCGA-L9-A444-01A-21D-A24D-08 TCGA-L9-A444-10A-01D-A24F-08 g.chr19:5455880C>A c.378C>A c.(376-378)ccC>ccA p.P126P LUAD 19 5456135 5456135 + Silent SNP A A C TCGA-86-8056-01A-11D-2238-08 TCGA-86-8056-10A-01D-2238-08 g.chr19:5456135A>C c.633A>C c.(631-633)tcA>tcC p.S211S LUAD 19 5456148 5456148 + Missense_Mutation SNP G G A TCGA-93-8067-01A-11D-2284-08 TCGA-93-8067-10A-01D-2284-08 g.chr19:5456148G>A c.646G>A c.(646-648)Gag>Aag p.E216K LUAD 19 5456195 5456195 + Silent SNP G G T TCGA-05-4250-01A-01D-1105-08 TCGA-05-4250-10A-01D-1105-08 g.chr19:5456195G>T c.693G>T c.(691-693)tcG>tcT p.S231S LUAD 19 5456203 5456203 + Missense_Mutation SNP C C T TCGA-86-7954-01A-11D-2184-08 TCGA-86-7954-10A-01D-2184-08 g.chr19:5456203C>T c.701C>T c.(700-702)gCg>gTg p.A234V LUAD 19 5456227 5456227 + Missense_Mutation SNP C C T TCGA-86-A4JF-01A-11D-A24P-08 TCGA-86-A4JF-10A-01D-A24P-08 g.chr19:5456227C>T c.725C>T c.(724-726)cCg>cTg p.P242L LUAD 19 5456253 5456253 + Missense_Mutation SNP G G C TCGA-78-7633-01A-11D-2063-08 TCGA-78-7633-10A-01D-2063-08 g.chr19:5456253G>C c.751G>C c.(751-753)Gtg>Ctg p.V251L LUAD 19 5456379 5456379 + Missense_Mutation SNP A A T TCGA-55-A490-01A-11D-A24D-08 TCGA-55-A490-10A-01D-A24F-08 g.chr19:5456379A>T c.877A>T c.(877-879)Acc>Tcc p.T293S LUAD 19 5456384 5456384 + Silent SNP C C T TCGA-91-A4BC-01A-11D-A24D-08 TCGA-91-A4BC-10A-01D-A24F-08 g.chr19:5456384C>T c.882C>T c.(880-882)tgC>tgT p.C294C LUAD 19 5456479 5456479 + Missense_Mutation SNP C C A TCGA-17-Z025-01A-01W-0746-08 TCGA-17-Z025-11A-01W-0746-08 g.chr19:5456479C>A c.977C>A c.(976-978)cCc>cAc p.P326H LUAD 19 5456536 5456536 + Missense_Mutation SNP G G A TCGA-69-7980-01A-11D-2184-08 TCGA-69-7980-10A-01D-2184-08 g.chr19:5456536G>A c.1034G>A c.(1033-1035)cGg>cAg p.R345Q LUAD 19 5456735 5456735 + Silent SNP C C A TCGA-55-A490-01A-11D-A24D-08 TCGA-55-A490-10A-01D-A24F-08 g.chr19:5456735C>A c.1233C>A c.(1231-1233)tcC>tcA p.S411S LUSC 19 5455728 5455728 + Missense_Mutation SNP C C A TCGA-34-5239-01A-21D-1817-08 TCGA-34-5239-10A-01D-1817-08 g.chr19:5455728C>A c.226C>A c.(226-228)Ccg>Acg p.P76T LUSC 19 5456134 5456134 + Missense_Mutation SNP C C T TCGA-46-3769-01A-01D-0983-08 TCGA-46-3769-10A-01D-0983-08 g.chr19:5456134C>T c.632C>T c.(631-633)tCa>tTa p.S211L LUSC 19 5456269 5456269 + Missense_Mutation SNP G G C TCGA-43-5668-01A-01D-1632-08 TCGA-43-5668-11A-01D-1632-08 g.chr19:5456269G>C c.767G>C c.(766-768)tGg>tCg p.W256S PAAD 19 5455699 5455699 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr19:5455699C>T c.197C>T c.(196-198)gCg>gTg p.A66V PAAD 19 5455843 5455843 + Missense_Mutation SNP C C T TCGA-H8-A6C1-01A-11D-A32N-08 TCGA-H8-A6C1-10A-01D-A32N-08 g.chr19:5455843C>T c.341C>T c.(340-342)gCg>gTg p.A114V PAAD 19 5456539 5456539 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr19:5456539G>A c.1037G>A c.(1036-1038)cGc>cAc p.R346H PAAD 19 5456659 5456659 + Missense_Mutation SNP T T C TCGA-2J-AABV-01A-12D-A40W-08 TCGA-2J-AABV-10A-01D-A40W-08 g.chr19:5456659T>C c.1157T>C c.(1156-1158)aTt>aCt p.I386T PRAD 19 5455562 5455562 + Silent SNP G G A TCGA-EJ-7314-01A-31D-2114-08 TCGA-EJ-7314-10A-01D-2114-08 g.chr19:5455562G>A c.60G>A c.(58-60)gcG>gcA p.A20A PRAD 19 5455959 5455959 + Missense_Mutation SNP C C T TCGA-ZG-A9N3-01A-11D-A41K-08 TCGA-ZG-A9N3-10A-01D-A41N-08 g.chr19:5455959C>T c.457C>T c.(457-459)Cgc>Tgc p.R153C PRAD 19 5456787 5456787 + Nonsense_Mutation SNP C C T TCGA-EJ-5516-01A-01D-1576-08 TCGA-EJ-5516-10A-01D-1577-08 g.chr19:5456787C>T c.1285C>T c.(1285-1287)Cag>Tag p.Q429* READ 19 5455583 5455583 + Silent SNP G G A TCGA-F5-6465-01A-11D-1733-10 TCGA-F5-6465-10A-01D-1733-10 g.chr19:5455583G>A c.81G>A c.(79-81)gcG>gcA p.A27A READ 19 5455803 5455803 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr19:5455803C>T c.301C>T c.(301-303)Cgg>Tgg p.R101W SARC 19 5456046 5456046 + Missense_Mutation SNP G G A TCGA-DX-A1L3-01A-11D-A24N-09 TCGA-DX-A1L3-10A-01D-A24N-09 g.chr19:5456046G>A c.544G>A c.(544-546)Gcg>Acg p.A182T SARC 19 5456439 5456439 + Silent SNP C C T TCGA-DX-A6YX-01A-11D-A417-09 TCGA-DX-A6YX-10B-01D-A41A-09 g.chr19:5456439C>T c.937C>T c.(937-939)Ctg>Ttg p.L313L SARC 19 5456454 5456454 + Missense_Mutation SNP G G A TCGA-QC-A7B5-01A-11D-A33E-09 TCGA-QC-A7B5-11A-11D-A33H-09 g.chr19:5456454G>A c.952G>A c.(952-954)Gag>Aag p.E318K SKCM 19 5455836 5455836 + Missense_Mutation SNP G G A TCGA-DA-A1HW-06A-11D-A19A-08 TCGA-DA-A1HW-10A-01D-A19A-08 g.chr19:5455836G>A c.334G>A c.(334-336)Gac>Aac p.D112N SKCM 19 5455863 5455863 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr19:5455863G>A c.361G>A c.(361-363)Ggc>Agc p.G121S SKCM 19 5455864 5455864 + Missense_Mutation SNP G G T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr19:5455864G>T c.362G>T c.(361-363)gGc>gTc p.G121V SKCM 19 5455958 5455958 + Silent SNP C C T TCGA-EE-A29S-06A-11D-A197-08 TCGA-EE-A29S-10A-01D-A199-08 g.chr19:5455958C>T c.456C>T c.(454-456)aaC>aaT p.N152N SKCM 19 5455959 5455959 + Missense_Mutation SNP C C T TCGA-EE-A29S-06A-11D-A197-08 TCGA-EE-A29S-10A-01D-A199-08 g.chr19:5455959C>T c.457C>T c.(457-459)Cgc>Tgc p.R153C SKCM 19 5456044 5456044 + Missense_Mutation SNP A A C TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr19:5456044A>C c.542A>C c.(541-543)gAg>gCg p.E181A SKCM 19 5456053 5456053 + Missense_Mutation SNP T T G TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr19:5456053T>G c.551T>G c.(550-552)aTc>aGc p.I184S SKCM 19 5456081 5456081 + Silent SNP C C T TCGA-D3-A3ML-06A-11D-A21A-08 TCGA-D3-A3ML-10A-01D-A21A-08 g.chr19:5456081C>T c.579C>T c.(577-579)ctC>ctT p.L193L SKCM 19 5456123 5456123 + Silent SNP C C T TCGA-DA-A1I1-06A-12D-A196-08 TCGA-DA-A1I1-10A-01D-A198-08 g.chr19:5456123C>T c.621C>T c.(619-621)atC>atT p.I207I SKCM 19 5456123 5456123 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr19:5456123C>T c.621C>T c.(619-621)atC>atT p.I207I SKCM 19 5456284 5456284 + Missense_Mutation SNP C C T TCGA-EE-A2MC-06A-12D-A197-08 TCGA-EE-A2MC-10A-01D-A199-08 g.chr19:5456284C>T c.782C>T c.(781-783)aCc>aTc p.T261I SKCM 19 5456292 5456292 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr19:5456292C>T c.790C>T c.(790-792)Ctg>Ttg p.L264L SKCM 19 5456309 5456309 + Silent SNP C C T TCGA-D3-A3C8-06A-12D-A19A-08 TCGA-D3-A3C8-10A-01D-A19A-08 g.chr19:5456309C>T c.807C>T c.(805-807)ttC>ttT p.F269F SKCM 19 5456451 5456451 + Missense_Mutation SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr19:5456451G>A c.949G>A c.(949-951)Gag>Aag p.E317K SKCM 19 5456549 5456549 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr19:5456549C>T c.1047C>T c.(1045-1047)ccC>ccT p.P349P SKCM 19 5456559 5456559 + Missense_Mutation SNP C C G TCGA-ER-A198-06A-11D-A196-08 TCGA-ER-A198-10A-01D-A198-08 g.chr19:5456559C>G c.1057C>G c.(1057-1059)Cag>Gag p.Q353E SKCM 19 5456594 5456594 + Silent SNP C C T TCGA-ER-A198-06A-11D-A196-08 TCGA-ER-A198-10A-01D-A198-08 g.chr19:5456594C>T c.1092C>T c.(1090-1092)tcC>tcT p.S364S SKCM 19 5456609 5456609 + Silent SNP C C T TCGA-ER-A42L-06A-11D-A24R-08 TCGA-ER-A42L-10A-01D-A24R-08 g.chr19:5456609C>T c.1107C>T c.(1105-1107)ttC>ttT p.F369F SKCM 19 5456627 5456627 + Silent SNP C C T TCGA-EE-A3J5-06A-11D-A20D-08 TCGA-EE-A3J5-10A-01D-A20D-08 g.chr19:5456627C>T c.1125C>T c.(1123-1125)tcC>tcT p.S375S SKCM 19 5456633 5456633 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr19:5456633G>A c.1131G>A c.(1129-1131)ccG>ccA p.P377P SKCM 19 5456634 5456634 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr19:5456634G>A c.1132G>A c.(1132-1134)Ggc>Agc p.G378S SKCM 19 5456640 5456640 + Missense_Mutation SNP C C G TCGA-EE-A2GL-06A-11D-A196-08 TCGA-EE-A2GL-10A-01D-A198-08 g.chr19:5456640C>G c.1138C>G c.(1138-1140)Cgg>Ggg p.R380G

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 19 5456021 5456021 single base substitution G A synonymous_variant L173L 519G>A BLCA-US 19 5455804 5455804 single base substitution G A missense_variant R101Q 302G>A BRCA-EU 19 5450676 5450676 single base substitution G C upstream_gene_variant BRCA-EU 19 5451289 5451289 single base substitution C A upstream_gene_variant BRCA-EU 19 5452109 5452109 single base substitution C T upstream_gene_variant BRCA-EU 19 5452395 5452395 single base substitution C T upstream_gene_variant BRCA-EU 19 5452485 5452485 single base substitution C A upstream_gene_variant BRCA-EU 19 5453178 5453178 single base substitution C T upstream_gene_variant BRCA-EU 19 5453390 5453390 single base substitution T A upstream_gene_variant BRCA-EU 19 5454396 5454396 single base substitution C T upstream_gene_variant BRCA-EU 19 5454888 5454888 single base substitution G C upstream_gene_variant BRCA-EU 19 5455519 5455519 single base substitution C A missense_variant P6Q 17C>A BRCA-EU 19 5455915 5455915 single base substitution C A missense_variant P138Q 413C>A BRCA-EU 19 5456007 5456007 single base substitution G A missense_variant D169N 505G>A BRCA-EU 19 5456985 5456985 single base substitution G T downstream_gene_variant BRCA-EU 19 5457420 5457420 single base substitution G A downstream_gene_variant BRCA-EU 19 5457488 5457488 single base substitution G A downstream_gene_variant BRCA-EU 19 5457939 5457939 single base substitution G A downstream_gene_variant BRCA-EU 19 5459192 5459192 single base substitution T C downstream_gene_variant BRCA-EU 19 5459391 5459391 single base substitution G A downstream_gene_variant BRCA-EU 19 5460261 5460261 single base substitution C T downstream_gene_variant BRCA-EU 19 5460477 5460477 single base substitution G C downstream_gene_variant BRCA-EU 19 5460765 5460765 single base substitution G T downstream_gene_variant BRCA-FR 19 5456007 5456007 single base substitution G A missense_variant D169N 505G>A BRCA-FR 19 5460477 5460477 single base substitution G C downstream_gene_variant BRCA-UK 19 5460928 5460928 single base substitution G A downstream_gene_variant BRCA-UK 19 5461826 5461826 single base substitution C A downstream_gene_variant BRCA-US 19 5455667 5455667 single base substitution G A synonymous_variant P55P 165G>A BRCA-US 19 5455855 5455855 single base substitution C T missense_variant A118V 353C>T BRCA-US 19 5455986 5455986 single base substitution C T missense_variant R162C 484C>T BRCA-US 19 5456398 5456398 single base substitution T A missense_variant V299D 896T>A BRCA-US 19 5456459 5456459 insertion of <=200bp - T frameshift_variant G319G? BTCA-JP 19 5455862 5455862 single base substitution C T synonymous_variant F120F 360C>T BTCA-JP 19 5456154 5456154 single base substitution G A missense_variant A218T 652G>A BTCA-JP 19 5456234 5456234 single base substitution C T synonymous_variant H244H 732C>T BTCA-JP 19 5456402 5456402 single base substitution C T synonymous_variant R300R 900C>T BTCA-JP 19 5456698 5456698 single base substitution G A missense_variant G399D 1196G>A CESC-US 19 5455848 5455848 single base substitution C T synonymous_variant L116L 346C>T CESC-US 19 5456111 5456111 single base substitution G A synonymous_variant L203L 609G>A CESC-US 19 5456144 5456144 single base substitution G T synonymous_variant V214V 642G>T CESC-US 19 5456482 5456482 single base substitution G A missense_variant C327Y 980G>A CLLE-ES 19 5451762 5451762 single base substitution G A upstream_gene_variant CLLE-ES 19 5452505 5452505 single base substitution C T upstream_gene_variant CLLE-ES 19 5453545 5453545 single base substitution C A upstream_gene_variant CLLE-ES 19 5460840 5460840 single base substitution G T downstream_gene_variant COAD-US 19 5455611 5455611 single base substitution C T missense_variant P37S 109C>T COAD-US 19 5455704 5455704 single base substitution C T missense_variant R68W 202C>T COAD-US 19 5455735 5455735 single base substitution G A missense_variant R78Q 233G>A COAD-US 19 5455771 5455771 single base substitution C T missense_variant S90L 269C>T COAD-US 19 5455796 5455796 single base substitution A G synonymous_variant A98A 294A>G COAD-US 19 5455868 5455868 deletion of <=200bp C - frameshift_variant V122 COAD-US 19 5455880 5455880 single base substitution C T synonymous_variant P126P 378C>T COAD-US 19 5455971 5455971 single base substitution G T missense_variant A157S 469G>T COAD-US 19 5455976 5455976 single base substitution C T synonymous_variant I158I 474C>T COAD-US 19 5455978 5455978 single base substitution T C missense_variant V159A 476T>C COAD-US 19 5455990 5455990 single base substitution G A missense_variant R163H 488G>A COAD-US 19 5456159 5456159 single base substitution G A synonymous_variant S219S 657G>A COAD-US 19 5456201 5456201 single base substitution C T synonymous_variant H233H 699C>T COAD-US 19 5456450 5456450 single base substitution T C synonymous_variant Y316Y 948T>C COAD-US 19 5456550 5456550 single base substitution G A missense_variant V350M 1048G>A COCA-CN 19 5456042 5456042 single base substitution C T synonymous_variant F180F 540C>T COCA-CN 19 5456063 5456063 single base substitution C T synonymous_variant N187N 561C>T COCA-CN 19 5456166 5456166 single base substitution C T synonymous_variant L222L 664C>T COCA-CN 19 5456297 5456297 single base substitution C T synonymous_variant V265V 795C>T COCA-CN 19 5456930 5456930 single base substitution A C downstream_gene_variant ESAD-UK 19 5450676 5450676 single base substitution G A upstream_gene_variant ESAD-UK 19 5453853 5453853 single base substitution T C upstream_gene_variant ESAD-UK 19 5455317 5455317 single base substitution A C upstream_gene_variant ESAD-UK 19 5455757 5455757 single base substitution C T synonymous_variant A85A 255C>T ESAD-UK 19 5455832 5455832 single base substitution G A synonymous_variant S110S 330G>A ESAD-UK 19 5455866 5455866 single base substitution G A missense_variant V122I 364G>A ESAD-UK 19 5456171 5456171 single base substitution G A synonymous_variant R223R 669G>A ESAD-UK 19 5456374 5456374 single base substitution C T missense_variant T291M 872C>T ESAD-UK 19 5456963 5456963 single base substitution C T downstream_gene_variant ESAD-UK 19 5458520 5458520 single base substitution C G downstream_gene_variant ESCA-CN 19 5455706 5455706 single base substitution G C synonymous_variant R68R 204G>C ESCA-CN 19 5455925 5455925 single base substitution G A synonymous_variant A141A 423G>A LAML-KR 19 5455871 5455871 single base substitution C T synonymous_variant P123P 369C>T LAML-KR 19 5456297 5456297 single base substitution C T synonymous_variant V265V 795C>T LICA-FR 19 5452874 5452874 single base substitution T C upstream_gene_variant LICA-FR 19 5455771 5455771 single base substitution C A stop_gained S90* 269C>A LICA-FR 19 5456054 5456054 single base substitution C T synonymous_variant I184I 552C>T LICA-FR 19 5456069 5456069 single base substitution C T synonymous_variant H189H 567C>T LICA-FR 19 5457788 5457788 insertion of <=200bp - AA downstream_gene_variant LIHC-US 19 5455751 5455751 single base substitution C T synonymous_variant V83V 249C>T LIHC-US 19 5456001 5456001 single base substitution A T missense_variant T167S 499A>T LINC-JP 19 5456121 5456121 single base substitution A G missense_variant I207V 619A>G LINC-JP 19 5456585 5456585 single base substitution C T synonymous_variant S361S 1083C>T LIRI-JP 19 5450717 5450717 single base substitution T C upstream_gene_variant LIRI-JP 19 5452071 5452071 single base substitution C T upstream_gene_variant LIRI-JP 19 5453378 5453378 single base substitution G T upstream_gene_variant LIRI-JP 19 5454009 5454009 single base substitution G A upstream_gene_variant LIRI-JP 19 5454229 5454229 single base substitution G A upstream_gene_variant LIRI-JP 19 5454284 5454284 single base substitution A G upstream_gene_variant LIRI-JP 19 5454588 5454588 single base substitution G T upstream_gene_variant LIRI-JP 19 5456909 5456909 single base substitution G A downstream_gene_variant LIRI-JP 19 5457497 5457497 single base substitution C T downstream_gene_variant LIRI-JP 19 5457547 5457547 single base substitution T C downstream_gene_variant LIRI-JP 19 5459828 5459828 single base substitution A G downstream_gene_variant LUSC-KR 19 5454493 5454493 single base substitution A T upstream_gene_variant LUSC-KR 19 5455735 5455735 single base substitution G A missense_variant R78Q 233G>A LUSC-KR 19 5456810 5456810 single base substitution G A 3_prime_UTR_variant LUSC-KR 19 5461194 5461194 single base substitution G A downstream_gene_variant LUSC-US 19 5455728 5455728 single base substitution C A missense_variant P76T 226C>A LUSC-US 19 5456134 5456134 single base substitution C T missense_variant S211L 632C>T LUSC-US 19 5456269 5456269 single base substitution G C missense_variant W256S 767G>C MALY-DE 19 5451608 5451608 single base substitution T C upstream_gene_variant MALY-DE 19 5452021 5452021 single base substitution C G upstream_gene_variant MALY-DE 19 5459625 5459625 single base substitution C T downstream_gene_variant MELA-AU 19 5450456 5450456 single base substitution G A upstream_gene_variant MELA-AU 19 5451116 5451116 single base substitution C T upstream_gene_variant MELA-AU 19 5451155 5451155 single base substitution C T upstream_gene_variant MELA-AU 19 5451315 5451315 single base substitution G A upstream_gene_variant MELA-AU 19 5451418 5451418 single base substitution G A upstream_gene_variant MELA-AU 19 5451782 5451782 single base substitution G A upstream_gene_variant MELA-AU 19 5451884 5451884 single base substitution T C upstream_gene_variant MELA-AU 19 5451908 5451908 single base substitution G A upstream_gene_variant MELA-AU 19 5452089 5452089 single base substitution A G upstream_gene_variant MELA-AU 19 5452269 5452269 single base substitution G A upstream_gene_variant MELA-AU 19 5452380 5452380 single base substitution C T upstream_gene_variant MELA-AU 19 5452493 5452493 single base substitution G A upstream_gene_variant MELA-AU 19 5452723 5452723 single base substitution G A upstream_gene_variant MELA-AU 19 5452778 5452778 single base substitution C T upstream_gene_variant MELA-AU 19 5452816 5452816 single base substitution C T upstream_gene_variant MELA-AU 19 5452951 5452951 single base substitution T C upstream_gene_variant MELA-AU 19 5453147 5453147 single base substitution G A upstream_gene_variant MELA-AU 19 5453269 5453269 single base substitution G A upstream_gene_variant MELA-AU 19 5453558 5453558 single base substitution G A upstream_gene_variant MELA-AU 19 5453582 5453582 single base substitution G A upstream_gene_variant MELA-AU 19 5453659 5453659 single base substitution C T upstream_gene_variant MELA-AU 19 5453681 5453681 single base substitution G A upstream_gene_variant MELA-AU 19 5453883 5453883 single base substitution T A upstream_gene_variant MELA-AU 19 5454030 5454030 single base substitution G A upstream_gene_variant MELA-AU 19 5454294 5454294 single base substitution C T upstream_gene_variant MELA-AU 19 5454488 5454488 single base substitution G A upstream_gene_variant MELA-AU 19 5454528 5454528 single base substitution G A upstream_gene_variant MELA-AU 19 5454576 5454576 single base substitution G A upstream_gene_variant MELA-AU 19 5454582 5454582 single base substitution C T upstream_gene_variant MELA-AU 19 5454616 5454616 single base substitution G A upstream_gene_variant MELA-AU 19 5454912 5454912 single base substitution T G upstream_gene_variant MELA-AU 19 5454918 5454918 single base substitution G A upstream_gene_variant MELA-AU 19 5454955 5454955 single base substitution G T upstream_gene_variant MELA-AU 19 5455034 5455035 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 19 5455060 5455060 single base substitution C T upstream_gene_variant MELA-AU 19 5455182 5455182 single base substitution C T upstream_gene_variant MELA-AU 19 5455212 5455212 single base substitution G A upstream_gene_variant MELA-AU 19 5455835 5455835 single base substitution G A synonymous_variant V111V 333G>A MELA-AU 19 5455976 5455976 single base substitution C T synonymous_variant I158I 474C>T MELA-AU 19 5456220 5456220 single base substitution G A missense_variant D240N 718G>A MELA-AU 19 5456333 5456333 single base substitution C T synonymous_variant L277L 831C>T MELA-AU 19 5456474 5456474 single base substitution C T synonymous_variant I324I 972C>T MELA-AU 19 5456485 5456485 single base substitution C T missense_variant S328F 983C>T MELA-AU 19 5456616 5456616 single base substitution G A missense_variant E372K 1114G>A MELA-AU 19 5456734 5456734 single base substitution C T missense_variant S411F 1232C>T MELA-AU 19 5456806 5456806 single base substitution G A 3_prime_UTR_variant MELA-AU 19 5457061 5457061 single base substitution C T downstream_gene_variant MELA-AU 19 5457209 5457209 single base substitution C T downstream_gene_variant MELA-AU 19 5457231 5457231 single base substitution G A downstream_gene_variant MELA-AU 19 5457253 5457253 single base substitution G A downstream_gene_variant MELA-AU 19 5457342 5457342 single base substitution C T downstream_gene_variant MELA-AU 19 5457396 5457396 single base substitution G A downstream_gene_variant MELA-AU 19 5457454 5457454 single base substitution T A downstream_gene_variant MELA-AU 19 5457683 5457683 single base substitution C T downstream_gene_variant MELA-AU 19 5457891 5457891 single base substitution G A downstream_gene_variant MELA-AU 19 5458733 5458733 single base substitution G A downstream_gene_variant MELA-AU 19 5458846 5458846 single base substitution C T downstream_gene_variant MELA-AU 19 5458857 5458857 single base substitution G A downstream_gene_variant MELA-AU 19 5458892 5458892 single base substitution C T downstream_gene_variant MELA-AU 19 5458958 5458958 single base substitution C T downstream_gene_variant MELA-AU 19 5458992 5458992 single base substitution G A downstream_gene_variant MELA-AU 19 5459020 5459020 single base substitution C T downstream_gene_variant MELA-AU 19 5459132 5459132 single base substitution G A downstream_gene_variant MELA-AU 19 5459163 5459163 single base substitution C T downstream_gene_variant MELA-AU 19 5459267 5459267 single base substitution G A downstream_gene_variant MELA-AU 19 5459359 5459359 single base substitution G A downstream_gene_variant MELA-AU 19 5459618 5459618 single base substitution C T downstream_gene_variant MELA-AU 19 5459804 5459804 single base substitution C T downstream_gene_variant MELA-AU 19 5459944 5459944 single base substitution C T downstream_gene_variant MELA-AU 19 5460005 5460005 single base substitution G A downstream_gene_variant MELA-AU 19 5460122 5460122 single base substitution G A downstream_gene_variant MELA-AU 19 5460140 5460140 single base substitution G A downstream_gene_variant MELA-AU 19 5460148 5460148 single base substitution C T downstream_gene_variant MELA-AU 19 5460466 5460466 single base substitution G A downstream_gene_variant MELA-AU 19 5460584 5460584 single base substitution C T downstream_gene_variant MELA-AU 19 5460591 5460591 single base substitution G A downstream_gene_variant MELA-AU 19 5460623 5460623 single base substitution G A downstream_gene_variant MELA-AU 19 5460990 5460990 single base substitution C T downstream_gene_variant MELA-AU 19 5461019 5461019 single base substitution G A downstream_gene_variant MELA-AU 19 5461657 5461657 single base substitution G A downstream_gene_variant MELA-AU 19 5461747 5461747 single base substitution C T downstream_gene_variant MELA-AU 19 5461828 5461828 single base substitution C T downstream_gene_variant ORCA-IN 19 5455543 5455543 single base substitution G C missense_variant S14T 41G>C ORCA-IN 19 5456741 5456741 single base substitution G T missense_variant E413D 1239G>T OV-AU 19 5452022 5452022 single base substitution T G upstream_gene_variant OV-AU 19 5454600 5454600 single base substitution G C upstream_gene_variant OV-AU 19 5457369 5457369 single base substitution T C downstream_gene_variant OV-AU 19 5458001 5458001 single base substitution T C downstream_gene_variant OV-AU 19 5461644 5461644 single base substitution T C downstream_gene_variant OV-AU 19 5461714 5461714 single base substitution C T downstream_gene_variant PACA-AU 19 5455607 5455607 single base substitution G A synonymous_variant S35S 105G>A PACA-AU 19 5455639 5455639 single base substitution G A missense_variant R46Q 137G>A PACA-AU 19 5455789 5455789 single base substitution C T missense_variant A96V 287C>T PACA-AU 19 5455844 5455844 single base substitution G A synonymous_variant A114A 342G>A PACA-AU 19 5455866 5455866 single base substitution G A missense_variant V122I 364G>A PACA-AU 19 5456420 5456420 single base substitution C T synonymous_variant N306N 918C>T PACA-AU 19 5457136 5457136 single base substitution T C downstream_gene_variant PACA-AU 19 5457306 5457306 single base substitution C A downstream_gene_variant PACA-AU 19 5457934 5457934 single base substitution A C downstream_gene_variant PACA-AU 19 5458655 5458655 single base substitution C G downstream_gene_variant PACA-AU 19 5461821 5461821 deletion of <=200bp C - downstream_gene_variant PACA-CA 19 5450564 5450564 single base substitution A G upstream_gene_variant PACA-CA 19 5452797 5452797 single base substitution G A upstream_gene_variant PACA-CA 19 5454335 5454335 single base substitution G A upstream_gene_variant PACA-CA 19 5454769 5454769 single base substitution G A upstream_gene_variant PACA-CA 19 5455729 5455729 single base substitution C T missense_variant P76L 227C>T PACA-CA 19 5456632 5456632 single base substitution C T missense_variant P377L 1130C>T PACA-CA 19 5456732 5456732 single base substitution G A synonymous_variant T410T 1230G>A PACA-CA 19 5457398 5457398 single base substitution C G downstream_gene_variant PACA-CA 19 5457806 5457806 single base substitution T A downstream_gene_variant PACA-CA 19 5458832 5458832 single base substitution C T downstream_gene_variant PACA-CA 19 5458959 5458959 single base substitution G A downstream_gene_variant PACA-CA 19 5459146 5459146 single base substitution C T downstream_gene_variant PACA-CA 19 5459383 5459383 single base substitution G T downstream_gene_variant PACA-CA 19 5459391 5459391 single base substitution G A downstream_gene_variant PACA-CA 19 5461130 5461130 single base substitution C T downstream_gene_variant PACA-CA 19 5461581 5461581 single base substitution A G downstream_gene_variant PAEN-AU 19 5452487 5452487 single base substitution C T upstream_gene_variant PBCA-DE 19 5450946 5450946 single base substitution A G upstream_gene_variant PBCA-DE 19 5453076 5453076 single base substitution C T upstream_gene_variant PBCA-DE 19 5458145 5458145 single base substitution G A downstream_gene_variant PBCA-DE 19 5459245 5459245 single base substitution C G downstream_gene_variant PRAD-US 19 5455562 5455562 single base substitution G A synonymous_variant A20A 60G>A PRAD-US 19 5456787 5456787 single base substitution C T stop_gained Q429* 1285C>T READ-US 19 5455583 5455583 single base substitution G A synonymous_variant A27A 81G>A READ-US 19 5456043 5456043 single base substitution G A missense_variant E181K 541G>A RECA-EU 19 5452054 5452054 single base substitution C T upstream_gene_variant RECA-EU 19 5453383 5453383 single base substitution G T upstream_gene_variant RECA-EU 19 5461376 5461376 single base substitution T A downstream_gene_variant SKCA-BR 19 5451804 5451804 single base substitution A G upstream_gene_variant SKCA-BR 19 5452410 5452410 single base substitution C T upstream_gene_variant SKCA-BR 19 5453713 5453713 single base substitution A C upstream_gene_variant SKCA-BR 19 5453817 5453817 single base substitution G A upstream_gene_variant SKCA-BR 19 5456235 5456235 single base substitution G A missense_variant D245N 733G>A SKCA-BR 19 5456442 5456442 single base substitution G A missense_variant D314N 940G>A SKCA-BR 19 5459020 5459020 single base substitution C T downstream_gene_variant SKCA-BR 19 5460346 5460346 single base substitution C T downstream_gene_variant SKCA-BR 19 5460379 5460379 single base substitution C T downstream_gene_variant SKCA-BR 19 5460686 5460686 single base substitution G A downstream_gene_variant SKCA-BR 19 5461461 5461461 single base substitution G A downstream_gene_variant SKCA-BR 19 5461694 5461694 single base substitution G T downstream_gene_variant SKCA-BR 19 5461785 5461785 single base substitution A G downstream_gene_variant SKCM-US 19 5455650 5455650 single base substitution A T stop_gained K50* 148A>T SKCM-US 19 5455739 5455739 single base substitution C T synonymous_variant A79A 237C>T SKCM-US 19 5455836 5455836 single base substitution G A missense_variant D112N 334G>A SKCM-US 19 5456044 5456044 single base substitution A C missense_variant E181A 542A>C SKCM-US 19 5456053 5456053 single base substitution T G missense_variant I184S 551T>G SKCM-US 19 5456054 5456054 single base substitution C T synonymous_variant I184I 552C>T SKCM-US 19 5456081 5456081 single base substitution C T synonymous_variant L193L 579C>T SKCM-US 19 5456123 5456123 single base substitution C T synonymous_variant I207I 621C>T SKCM-US 19 5456251 5456251 single base substitution C A missense_variant P250H 749C>A SKCM-US 19 5456284 5456284 single base substitution C T missense_variant T261I 782C>T SKCM-US 19 5456292 5456292 single base substitution C T synonymous_variant L264L 790C>T SKCM-US 19 5456309 5456309 single base substitution C T synonymous_variant F269F 807C>T SKCM-US 19 5456451 5456451 single base substitution G A missense_variant E317K 949G>A SKCM-US 19 5456549 5456549 single base substitution C T synonymous_variant P349P 1047C>T SKCM-US 19 5456559 5456559 single base substitution C G missense_variant Q353E 1057C>G SKCM-US 19 5456594 5456594 single base substitution C T synonymous_variant S364S 1092C>T SKCM-US 19 5456627 5456627 single base substitution C T synonymous_variant S375S 1125C>T SKCM-US 19 5456640 5456640 single base substitution C G missense_variant R380G 1138C>G STAD-US 19 5455507 5455507 single base substitution C T missense_variant P2L 5C>T STAD-US 19 5455562 5455562 single base substitution G A synonymous_variant A20A 60G>A STAD-US 19 5455652 5455652 single base substitution G T missense_variant K50N 150G>T STAD-US 19 5455726 5455726 single base substitution G A missense_variant R75Q 224G>A STAD-US 19 5455855 5455855 single base substitution C T missense_variant A118V 353C>T STAD-US 19 5455890 5455890 single base substitution C T missense_variant R130W 388C>T STAD-US 19 5456007 5456007 single base substitution G A missense_variant D169N 505G>A STAD-US 19 5456055 5456055 single base substitution G A missense_variant V185M 553G>A STAD-US 19 5456204 5456204 single base substitution G A synonymous_variant A234A 702G>A STAD-US 19 5456241 5456241 single base substitution G T missense_variant G247C 739G>T STAD-US 19 5456475 5456475 single base substitution C A missense_variant L325M 973C>A STAD-US 19 5456550 5456550 single base substitution G A missense_variant V350M 1048G>A STAD-US 19 5456563 5456563 single base substitution C T missense_variant S354L 1061C>T STAD-US 19 5456567 5456567 single base substitution G A synonymous_variant V355V 1065G>A STAD-US 19 5456633 5456633 single base substitution G A synonymous_variant P377P 1131G>A THCA-US 19 5455622 5455622 single base substitution G A synonymous_variant R40R 120G>A UCEC-US 19 5456550 5456550 single base substitution G A missense_variant V350M 1048G>A UCEC-US 19 5456656 5456656 single base substitution C T missense_variant A385V 1154C>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-46-3769-01 COSM713815 c.632C>T p.S211L Substitution - Missense 19:5456123-5456123 + LUAD-S01345 COSM397033 c.1159C>G p.Q387E Substitution - Missense 19:5456650-5456650 + TCGA-D5-6537-01 COSM3757177 c.469G>T p.A157S Substitution - Missense 19:5455960-5455960 + PD9595a COSM5776013 c.413C>A p.P138Q Substitution - Missense 19:5455904-5455904 + cSCCP1 COSM135803 c.715G>A p.D239N Substitution - Missense 19:5456206-5456206 + TCGA-EE-A2MR-06 COSM3538573 c.949G>A p.E317K Substitution - Missense 19:5456440-5456440 + TCGA-AA-3712-01 COSM3757177 c.469G>T p.A157S Substitution - Missense 19:5455960-5455960 + T3190 COSM4745333 c.283C>T p.P95S Substitution - Missense 19:5455774-5455774 + 1_PRE-TREATMENT COSM1721120 c.122C>T p.P41L Substitution - Missense 19:5455613-5455613 + TCGA-A6-6780-01 COSM3757181 c.657G>A p.S219S Substitution - coding silent 19:5456148-5456148 + PD11745a COSM5796270 c.17C>A p.P6Q Substitution - Missense 19:5455508-5455508 + CN-AML-NR-08-Dx COSM2929433 c.369C>T p.P123P Substitution - coding silent 19:5455860-5455860 + TCGA-FW-A3R5-06 COSM2929468 c.1047C>T p.P349P Substitution - coding silent 19:5456538-5456538 + TCGA-AM-5821-01 COSM3757182 c.948T>C p.Y316Y Substitution - coding silent 19:5456439-5456439 + HCC88T COSM1612762 c.1083C>T p.S361S Substitution - coding silent 19:5456574-5456574 + TCGA-EK-A2R8-01 COSM4822590 c.642G>T p.V214V Substitution - coding silent 19:5456133-5456133 + 8066500 COSM1234783 c.137G>A p.R46Q Substitution - Missense 19:5455628-5455628 + TCGA-D5-6930-01 COSM1234782 c.202C>T p.R68W Substitution - Missense 19:5455693-5455693 + HN_62493 COSM126522 c.622G>A p.A208T Substitution - Missense 19:5456113-5456113 + TCGA-BR-4370-01 COSM4081159 c.224G>A p.R75Q Substitution - Missense 19:5455715-5455715 + TCGA-CC-A7IH-01 COSM4924350 c.249C>T p.V83V Substitution - coding silent 19:5455740-5455740 + SNUH_G10_S1 COSM3757177 c.469G>T p.A157S Substitution - Missense 19:5455960-5455960 + TCGA-BF-A1PV-01 COSM3538565 c.237C>T p.A79A Substitution - coding silent 19:5455728-5455728 + LUAD-S01404 COSM398745 c.523G>A p.A175T Substitution - Missense 19:5456014-5456014 + PTC-54C COSM3757175 c.109C>T p.P37S Substitution - Missense 19:5455600-5455600 + TCGA-EE-A2MC-06 COSM3538572 c.782C>T p.T261I Substitution - Missense 19:5456273-5456273 + CN-AML-08-T COSM2929433 c.369C>T p.P123P Substitution - coding silent 19:5455860-5455860 + SJDES029 COSM4581387 c.422C>T p.A141V Substitution - Missense 19:5455913-5455913 + LIM1215 COSM4639463 c.171A>G p.P57P Substitution - coding silent 19:5455662-5455662 + Au1 COSM5597972 c.1114G>A p.E372K Substitution - Missense 19:5456605-5456605 + CSCC-31-T COSM4506217 c.713C>T p.P238L Substitution - Missense 19:5456204-5456204 + STC263 COSM3773152 c.105G>A p.S35S Substitution - coding silent 19:5455596-5455596 + 1_PRE-TREATMENT COSM1721122 c.661G>A p.D221N Substitution - Missense 19:5456152-5456152 + HCC65T COSM1612760 c.619A>G p.I207V Substitution - Missense 19:5456110-5456110 + BD124T COSM5493779 c.732C>T p.H244H Substitution - coding silent 19:5456223-5456223 + TCGA-DK-A3IU-01 COSM3797492 c.302G>A p.R101Q Substitution - Missense 19:5455793-5455793 + T45458580 COSM5715376 c.1053C>A p.C351* Substitution - Nonsense 19:5456544-5456544 + 673 COSM1159837 c.41G>C p.S14T Substitution - Missense 19:5455532-5455532 + TCGA-BR-8487-01 COSM1471222 c.60G>A p.A20A Substitution - coding silent 19:5455551-5455551 + CHC1754T COSM3538567 c.552C>T p.I184I Substitution - coding silent 19:5456043-5456043 + TCGA-CD-8536-01 COSM4081160 c.388C>T p.R130W Substitution - Missense 19:5455879-5455879 + OSCC-GB_00190111 COSM1159837 c.41G>C p.S14T Substitution - Missense 19:5455532-5455532 + 8016470 COSM3389334 c.364G>A p.V122I Substitution - Missense 19:5455855-5455855 + T276 COSM4745335 c.444G>A p.P148P Substitution - coding silent 19:5455935-5455935 + EGC15 COSM1234783 c.137G>A p.R46Q Substitution - Missense 19:5455628-5455628 + 1115157 COSM5560321 c.586A>T p.M196L Substitution - Missense 19:5456077-5456077 + 35M COSM5583218 c.1176C>T p.S392S Substitution - coding silent 19:5456667-5456667 + TCGA-AA-3662-01 COSM3757177 c.469G>T p.A157S Substitution - Missense 19:5455960-5455960 + TCGA-D3-A2J8-06 COSM3538567 c.552C>T p.I184I Substitution - coding silent 19:5456043-5456043 + BD72T COSM5513441 c.1196G>A p.G399D Substitution - Missense 19:5456687-5456687 + TCGA-CJ-4904-01 COSM475229 c.1113C>T p.D371D Substitution - coding silent 19:5456604-5456604 + 587220 COSM1234782 c.202C>T p.R68W Substitution - Missense 19:5455693-5455693 + HCC65 COSM1612760 c.619A>G p.I207V Substitution - Missense 19:5456110-5456110 + TCGA-BR-8078-01 COSM4081167 c.1061C>T p.S354L Substitution - Missense 19:5456552-5456552 + TCGA-A3-3363-01 COSM1494445 c.912G>A p.W304* Substitution - Nonsense 19:5456403-5456403 + Pat_11_A COSM3686160 c.366delC p.L124fs*10 Deletion - Frameshift 19:5455857-5455857 + PCSI_0084_Pa_P_526 COSM3378952 c.227C>T p.P76L Substitution - Missense 19:5455718-5455718 + TCGA-D9-A6EC-06 COSM4405400 c.542A>C p.E181A Substitution - Missense 19:5456033-5456033 + TCGA-A6-6142-01 COSM1395135 c.699C>T p.H233H Substitution - coding silent 19:5456190-5456190 + CSCC-44-T COSM4503409 c.639C>T p.F213F Substitution - coding silent 19:5456130-5456130 + Au3 COSM5602675 c.1110G>A p.R370R Substitution - coding silent 19:5456601-5456601 + HCT8 COSM4634453 c.1078G>T p.D360Y Substitution - Missense 19:5456569-5456569 + TCGA-F5-6465-01 COSM1564327 c.81G>A p.A27A Substitution - coding silent 19:5455572-5455572 + SNUH_G10_S1 COSM440240 c.294A>G p.A98A Substitution - coding silent 19:5455785-5455785 + SNUH_G76_S1 COSM3757176 c.233G>A p.R78Q Substitution - Missense 19:5455724-5455724 + TCGA-BR-4362-01 COSM2929419 c.5C>T p.P2L Substitution - Missense 19:5455496-5455496 + CHC1085T COSM4788672 c.269C>A p.S90* Substitution - Nonsense 19:5455760-5455760 + 8066738 COSM3773152 c.105G>A p.S35S Substitution - coding silent 19:5455596-5455596 + T3267 COSM2929422 c.80C>T p.A27V Substitution - Missense 19:5455571-5455571 + TCGA-AM-5821-01 COSM3757175 c.109C>T p.P37S Substitution - Missense 19:5455600-5455600 + TCGA-AP-A0LM-01 COSM50632 c.1048G>A p.V350M Substitution - Missense 19:5456539-5456539 + 66 COSM50632 c.1048G>A p.V350M Substitution - Missense 19:5456539-5456539 + 677 COSM1159837 c.41G>C p.S14T Substitution - Missense 19:5455532-5455532 + HCC88 COSM1612762 c.1083C>T p.S361S Substitution - coding silent 19:5456574-5456574 + ESO-003 COSM1271974 c.872C>T p.T291M Substitution - Missense 19:5456363-5456363 + PT14_1 COSM4081161 c.505G>A p.D169N Substitution - Missense 19:5455996-5455996 + Au3 COSM5602674 c.1280C>T p.P427L Substitution - Missense 19:5456771-5456771 + TCGA-BP-4983-01 COSM50633 c.1130C>A p.P377Q Substitution - Missense 19:5456621-5456621 + CSCC-27-T COSM4514671 c.983C>T p.S328F Substitution - Missense 19:5456474-5456474 + 426 COSM4432887 c.1062G>A p.S354S Substitution - coding silent 19:5456553-5456553 + TCGA-CG-4305-01 COSM50632 c.1048G>A p.V350M Substitution - Missense 19:5456539-5456539 + PCSI_0084_Pa_X COSM3378952 c.227C>T p.P76L Substitution - Missense 19:5455718-5455718 + PT26 COSM5597972 c.1114G>A p.E372K Substitution - Missense 19:5456605-5456605 + TCGA-A8-A07G-01 COSM5833858 c.957_958insT p.D320fs*1 Insertion - Frameshift 19:5456448-5456449 + 2492723 COSM3538566 c.334G>A p.D112N Substitution - Missense 19:5455825-5455825 + sysucc-274T COSM5476113 c.561C>T p.N187N Substitution - coding silent 19:5456052-5456052 + TCGA-AM-5821-01 COSM3757176 c.233G>A p.R78Q Substitution - Missense 19:5455724-5455724 + YUKAT COSM5390658 c.1124C>T p.S375F Substitution - Missense 19:5456615-5456615 + PDA_016 COSM3389334 c.364G>A p.V122I Substitution - Missense 19:5455855-5455855 + PTC-28C COSM3757179 c.476T>C p.V159A Substitution - Missense 19:5455967-5455967 + CSCC-27-T COSM4515717 c.1267_1268CC>TT p.P423F Substitution - Missense 19:5456758-5456759 + TCGA-AA-3712-01 COSM3757179 c.476T>C p.V159A Substitution - Missense 19:5455967-5455967 + 2492722 COSM3538566 c.334G>A p.D112N Substitution - Missense 19:5455825-5455825 + PT48 COSM5933980 c.1111G>A p.D371N Substitution - Missense 19:5456602-5456602 + YULETA COSM3538569 c.621C>T p.I207I Substitution - coding silent 19:5456112-5456112 + I2L-P10-Tumor-Organoid COSM4581387 c.422C>T p.A141V Substitution - Missense 19:5455913-5455913 + TCGA-D8-A13Z-01 COSM440242 c.896T>A p.V299D Substitution - Missense 19:5456387-5456387 + TCGA-EJ-7314-01 COSM1471222 c.60G>A p.A20A Substitution - coding silent 19:5455551-5455551 + T3064 COSM2929443 c.540C>T p.F180F Substitution - coding silent 19:5456031-5456031 + PTC-7C COSM3757175 c.109C>T p.P37S Substitution - Missense 19:5455600-5455600 + OSCC-GB_00640111 COSM4885157 c.1239G>T p.E413D Substitution - Missense 19:5456730-5456730 + 587336 COSM1234783 c.137G>A p.R46Q Substitution - Missense 19:5455628-5455628 + SC_9099 COSM5570631 c.365T>C p.V122A Substitution - Missense 19:5455856-5455856 + 587256 COSM1234784 c.746A>G p.H249R Substitution - Missense 19:5456237-5456237 + ESO-017 COSM1271975 c.957C>T p.G319G Substitution - coding silent 19:5456448-5456448 + Co108 COSM50632 c.1048G>A p.V350M Substitution - Missense 19:5456539-5456539 + Mx43 COSM50633 c.1130C>A p.P377Q Substitution - Missense 19:5456621-5456621 + SJHGG115_R COSM4971992 c.668G>A p.R223Q Substitution - Missense 19:5456159-5456159 + STC263 COSM50632 c.1048G>A p.V350M Substitution - Missense 19:5456539-5456539 + TCGA-A8-A09N-01 COSM440239 c.165G>A p.P55P Substitution - coding silent 19:5455656-5455656 + TCGA-BR-8487-01 COSM440241 c.353C>T p.A118V Substitution - Missense 19:5455844-5455844 + PT23_1 COSM5903237 c.940G>A p.D314N Substitution - Missense 19:5456431-5456431 + PTC-7C COSM3757182 c.948T>C p.Y316Y Substitution - coding silent 19:5456439-5456439 + 1_PRE-TREATMENT COSM1721121 c.513G>A p.K171K Substitution - coding silent 19:5456004-5456004 + TCGA-CG-5722-01 COSM4081164 c.702G>A p.A234A Substitution - coding silent 19:5456193-5456193 + TCGA-FW-A3R5-06 COSM3538569 c.621C>T p.I207I Substitution - coding silent 19:5456112-5456112 + SNUH_G10_S1 COSM3757179 c.476T>C p.V159A Substitution - Missense 19:5455967-5455967 + TCGA-G4-6321-01 COSM3757177 c.469G>T p.A157S Substitution - Missense 19:5455960-5455960 + 2492721 COSM3538566 c.334G>A p.D112N Substitution - Missense 19:5455825-5455825 + 1_RESISTANT COSM1721121 c.513G>A p.K171K Substitution - coding silent 19:5456004-5456004 + LS174T COSM2929430 c.288G>A p.A96A Substitution - coding silent 19:5455779-5455779 + LUAD-RT-S01813 COSM383215 c.273G>A p.L91L Substitution - coding silent 19:5455764-5455764 + S00539 COSM316943 c.51A>T p.P17P Substitution - coding silent 19:5455542-5455542 + TCGA-DA-A1I1-06 COSM3538569 c.621C>T p.I207I Substitution - coding silent 19:5456112-5456112 + TCGA-ER-A198-06 COSM3538574 c.1057C>G p.Q353E Substitution - Missense 19:5456548-5456548 + T3109 COSM4745336 c.570C>T p.S190S Substitution - coding silent 19:5456061-5456061 + TCGA-HU-A4GN-01 COSM4081165 c.739G>T p.G247C Substitution - Missense 19:5456230-5456230 + TCGA-BR-6452-01 COSM4081158 c.150G>T p.K50N Substitution - Missense 19:5455641-5455641 + S00539 COSM316943 c.51A>T p.P17P Substitution - coding silent 19:5455542-5455542 + 8058184 COSM3389333 c.342G>A p.A114A Substitution - coding silent 19:5455833-5455833 + LIM2551 COSM4644246 c.718G>A p.D240N Substitution - Missense 19:5456209-5456209 + CCK81 COSM2929435 c.387A>G p.I129M Substitution - Missense 19:5455878-5455878 + TCGA-EE-A2GL-06 COSM3538577 c.1138C>G p.R380G Substitution - Missense 19:5456629-5456629 + TCGA-DM-A1HA-01 COSM1395132 c.378C>T p.P126P Substitution - coding silent 19:5455869-5455869 + CHC1207T COSM4800033 c.567C>T p.H189H Substitution - coding silent 19:5456058-5456058 + TCGA-CK-4950-01 COSM440240 c.294A>G p.A98A Substitution - coding silent 19:5455785-5455785 + 417 COSM4431673 c.573C>T p.D191D Substitution - coding silent 19:5456064-5456064 + ESCC_BICR_013T COSM5439323 c.423G>A p.A141A Substitution - coding silent 19:5455914-5455914 + LUAD-F00282 COSM367204 c.986A>T p.H329L Substitution - Missense 19:5456477-5456477 + T3024 COSM4745337 c.614G>A p.G205D Substitution - Missense 19:5456105-5456105 + TCGA-AG-A002-01 COSM265205 c.301C>T p.R101W Substitution - Missense 19:5455792-5455792 + TCGA-EB-A3Y6-01 COSM3538571 c.749C>A p.P250H Substitution - Missense 19:5456240-5456240 + B59-3-Tumor COSM1751045 c.519G>A p.L173L Substitution - coding silent 19:5456010-5456010 + T26 COSM5343427 c.143G>A p.C48Y Substitution - Missense 19:5455634-5455634 + PTC-7C COSM440240 c.294A>G p.A98A Substitution - coding silent 19:5455785-5455785 + BD121T COSM5515679 c.360C>T p.F120F Substitution - coding silent 19:5455851-5455851 + TCGA-EJ-5516-01 COSM1129726 c.1285C>T p.Q429* Substitution - Nonsense 19:5456776-5456776 + TCGA-FW-A3R5-06 COSM3893361 c.790C>T p.L264L Substitution - coding silent 19:5456281-5456281 + TCGA-34-5239-01 COSM713816 c.226C>A p.P76T Substitution - Missense 19:5455717-5455717 + 435 COSM2929438 c.445C>T p.R149* Substitution - Nonsense 19:5455936-5455936 + BD236T COSM5519586 c.900C>T p.R300R Substitution - coding silent 19:5456391-5456391 + TCGA-G4-6320-01 COSM50632 c.1048G>A p.V350M Substitution - Missense 19:5456539-5456539 + TCGA-AY-6197-01 COSM3757180 c.488G>A p.R163H Substitution - Missense 19:5455979-5455979 + PTC-28C COSM4132421 c.599A>T p.Y200F Substitution - Missense 19:5456090-5456090 + TCGA-HU-8602-01 COSM4081162 c.553G>A p.V185M Substitution - Missense 19:5456044-5456044 + LP6005409-DNA_G03 COSM4409146 c.669G>A p.R223R Substitution - coding silent 19:5456160-5456160 + 61 COSM2929431 c.341C>T p.A114V Substitution - Missense 19:5455832-5455832 + 1_RESISTANT COSM1721122 c.661G>A p.D221N Substitution - Missense 19:5456152-5456152 + ESCC-243T COSM3938275 c.204G>C p.R68R Substitution - coding silent 19:5455695-5455695 + TCGA-AA-3712-01 COSM3757178 c.474C>T p.I158I Substitution - coding silent 19:5455965-5455965 + PTC-10C COSM3757182 c.948T>C p.Y316Y Substitution - coding silent 19:5456439-5456439 + 2492720 COSM3538566 c.334G>A p.D112N Substitution - Missense 19:5455825-5455825 + CHC1754T COSM3538567 c.552C>T p.I184I Substitution - coding silent 19:5456043-5456043 + CHC1207T COSM4800033 c.567C>T p.H189H Substitution - coding silent 19:5456058-5456058 + T2932 COSM4745334 c.329C>T p.S110L Substitution - Missense 19:5455820-5455820 + NOKSI COSM2929418 c.4C>T p.P2S Substitution - Missense 19:5455495-5455495 + EGC3 COSM4081162 c.553G>A p.V185M Substitution - Missense 19:5456044-5456044 + C008 COSM5524305 c.547G>A p.A183T Substitution - Missense 19:5456038-5456038 + TCGA-D3-A3C8-06 COSM3893362 c.807C>T p.F269F Substitution - coding silent 19:5456298-5456298 + PT20_1 COSM4506217 c.713C>T p.P238L Substitution - Missense 19:5456204-5456204 + TCGA-CA-6717-01 COSM3693055 c.269C>T p.S90L Substitution - Missense 19:5455760-5455760 + TCGA-B4-5838-01 COSM1494447 c.77A>G p.H26R Substitution - Missense 19:5455568-5455568 + TCGA-AX-A0J1-01 COSM1000953 c.1154C>T p.A385V Substitution - Missense 19:5456645-5456645 + 19T COSM1159837 c.41G>C p.S14T Substitution - Missense 19:5455532-5455532 + TCGA-EI-6917-01 COSM3423127 c.541G>A p.E181K Substitution - Missense 19:5456032-5456032 + PCSI_0164_Pa_P_526 COSM3787776 c.1130C>T p.P377L Substitution - Missense 19:5456621-5456621 + TCGA-EL-A3GY-01 COSM2929423 c.120G>A p.R40R Substitution - coding silent 19:5455611-5455611 + TCGA-BR-8361-01 COSM4081161 c.505G>A p.D169N Substitution - Missense 19:5455996-5455996 + TCGA-AK-3447-01 COSM1494446 c.828G>T p.W276C Substitution - Missense 19:5456319-5456319 + TCGA-BR-6564-01 COSM4081169 c.1131G>A p.P377P Substitution - coding silent 19:5456622-5456622 + TCGA-D9-A6EC-06 COSM4399949 c.551T>G p.I184S Substitution - Missense 19:5456042-5456042 + B59-3 COSM1751045 c.519G>A p.L173L Substitution - coding silent 19:5456010-5456010 + CSCC-31-T COSM4514378 c.972C>T p.I324I Substitution - coding silent 19:5456463-5456463 + 8049223 COSM2929429 c.287C>T p.A96V Substitution - Missense 19:5455778-5455778 + LS180 COSM2929430 c.288G>A p.A96A Substitution - coding silent 19:5455779-5455779 + TCGA-AO-A128-01 COSM3835659 c.484C>T p.R162C Substitution - Missense 19:5455975-5455975 + TCGA-D3-A3ML-06 COSM3538568 c.579C>T p.L193L Substitution - coding silent 19:5456070-5456070 + 8035328 COSM3389335 c.918C>T p.N306N Substitution - coding silent 19:5456409-5456409 + 1_RESISTANT COSM1721120 c.122C>T p.P41L Substitution - Missense 19:5455613-5455613 + TCGA-EE-A3J5-06 COSM3538576 c.1125C>T p.S375S Substitution - coding silent 19:5456616-5456616 + TCGA-HU-A4G8-01 COSM4081166 c.973C>A p.L325M Substitution - Missense 19:5456464-5456464 + TCGA-AA-3663-01 COSM3686160 c.366delC p.L124fs*10 Deletion - Frameshift 19:5455857-5455857 + TCGA-CG-4436-01 COSM4081168 c.1065G>A p.V355V Substitution - coding silent 19:5456556-5456556 + TCGA-AA-A02W-01 COSM301014 c.885G>A p.Q295Q Substitution - coding silent 19:5456376-5456376 + HT115 COSM2929467 c.1036C>T p.R346C Substitution - Missense 19:5456527-5456527 + SNUH_G16_S1 COSM4000909 c.487C>T p.R163C Substitution - Missense 19:5455978-5455978 + PCSI_0326_Pa_P_526 COSM4965306 c.1230G>A p.T410T Substitution - coding silent 19:5456721-5456721 + CHC197T COSM3757182 c.948T>C p.Y316Y Substitution - coding silent 19:5456439-5456439 + CHC1085T COSM4788672 c.269C>A p.S90* Substitution - Nonsense 19:5455760-5455760 + CHC320T COSM3757175 c.109C>T p.P37S Substitution - Missense 19:5455600-5455600 + CN-AML-CR-34-Dx COSM5425131 c.795C>T p.V265V Substitution - coding silent 19:5456286-5456286 + 11M COSM5577238 c.1237G>A p.E413K Substitution - Missense 19:5456728-5456728 + TCGA-DA-A1HW-06 COSM3538566 c.334G>A p.D112N Substitution - Missense 19:5455825-5455825 + TCGA-D5-6537-01 COSM3757179 c.476T>C p.V159A Substitution - Missense 19:5455967-5455967 + BD230T COSM5496753 c.652G>A p.A218T Substitution - Missense 19:5456143-5456143 + PTC-28C COSM3757178 c.474C>T p.I158I Substitution - coding silent 19:5455965-5455965 + TCGA-43-5668-01 COSM713813 c.767G>C p.W256S Substitution - Missense 19:5456258-5456258 + TCGA-UB-A7MB-01 COSM4931258 c.499A>T p.T167S Substitution - Missense 19:5455990-5455990 + 2557_CLM COSM5755463 c.1069G>A p.A357T Substitution - Missense 19:5456560-5456560 + TCGA-ER-A198-06 COSM3538575 c.1092C>T p.S364S Substitution - coding silent 19:5456583-5456583 + SE35PT COSM1579930 c.286G>A p.A96T Substitution - Missense 19:5455777-5455777 + TCGA-AA-3712-01 COSM440240 c.294A>G p.A98A Substitution - coding silent 19:5455785-5455785 + SNUH_G10_S1 COSM4000909 c.487C>T p.R163C Substitution - Missense 19:5455978-5455978 + TCGA-A8-A08H-01 COSM440241 c.353C>T p.A118V Substitution - Missense 19:5455844-5455844 + ME024T COSM226375 c.121C>T p.P41S Substitution - Missense 19:5455612-5455612 + TCGA-EB-A3Y6-01 COSM3538564 c.148A>T p.K50* Substitution - Nonsense 19:5455639-5455639 + TCGA-EK-A2PG-01 COSM4819656 c.346C>T p.L116L Substitution - coding silent 19:5455837-5455837 + 2293771 COSM4607238 c.529C>T p.R177C Substitution - Missense 19:5456020-5456020 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.126414;Hs.126415;Hs.126452;Hs.126467;Hs.126468;Hs.126473;Hs.126488;Hs.126491;Hs.126496 19p13.3 612063

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A T Synonymous p.P17P c.51A>T 19 5455553 SCLC C A Missense p.P326H c.977C>A 19 5456479 LUAD C A Missense p.P76T c.226C>A 19 5455728 LUSC C A Synonymous p.G156G c.468C>A 19 5455970 LUAD CC TT Missense p.R153C c.456_457delinsTT 19 5455958 CM C G Missense p.L116V c.346C>G 19 5455848 HNSC C G Missense p.Q353E c.1057C>G 19 5456559 CM C G Missense p.R380G c.1138C>G 19 5456640 CM C G Synonymous p.V83V c.249C>G 19 5455751 LUAD C T Missense p.A114V c.341C>T 19 5455843 HNSC C T Missense p.H249Y c.745C>T 19 5456247 CM C T Missense p.L3F c.7C>T 19 5455509 LUAD C T Missense p.P17S c.49C>T 19 5455551 CM C T Missense p.S211L c.632C>T 19 5456134 LUSC C T Missense p.T261I c.782C>T 19 5456284 CM C T Missense p.T291M c.872C>T 19 5456374 ESCA C T Nonsense p.Q429* c.1285C>T 19 5456787 PRAD C T Synonymous p.A79A c.237C>T 19 5455739 CM C T Synonymous p.F269F c.807C>T 19 5456309 CM C T Synonymous p.G319G c.957C>T 19 5456459 ESCA C T Synonymous p.I184I c.552C>T 19 5456054 CM C T Synonymous p.I207I c.621C>T 19 5456123 CM C T Synonymous p.L193L c.579C>T 19 5456081 CM C T Synonymous p.N140N c.420C>T 19 5455922 HNSC C T Synonymous p.P250P c.750C>T 19 5456252 CM C T Synonymous p.S195S c.585C>T 19 5456087 STAD C T Synonymous p.S364S c.1092C>T 19 5456594 CM C T Synonymous p.S375S c.1125C>T 19 5456627 CM C T Synonymous p.T301T c.903C>T 19 5456405 CM G A Missense p.A208T c.622G>A 19 5456124 HNSC G A Missense p.A218T c.652G>A 19 5456154 HNSC G A Missense p.D112N c.334G>A 19 5455836 CM G A Missense p.D191N c.571G>A 19 5456073 STAD G A Missense p.R101Q c.302G>A 19 5455804 BLCA G A Missense p.R75Q c.224G>A 19 5455726 STAD G A Missense p.V251M c.751G>A 19 5456253 HNSC G A Missense p.V254M c.760G>A 19 5456262 BRCA G A Missense p.V350M c.1048G>A 19 5456550 STAD G A Synonymous p.A20A c.60G>A 19 5455562 PRAD G A Synonymous p.A234A c.702G>A 19 5456204 STAD G A Synonymous p.P377P c.1131G>A 19 5456633 STAD G A Synonymous p.P55P c.165G>A 19 5455667 BRCA G A Synonymous p.Q295Q c.885G>A 19 5456387 COREAD G A Synonymous p.R40R c.120G>A 19 5455622 THCA G A Synonymous p.V355V c.1065G>A 19 5456567 STAD G A Synonymous p.V99V c.297G>A 19 5455799 CM G C Missense p.W256S c.767G>C 19 5456269 LUSC G T Synonymous p.S231S c.693G>T 19 5456195 LUAD T A Missense p.V299D c.896T>A 19 5456398 BRCA