Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change BLCA 6 138192400 138192400 + Missense_Mutation SNP G G C TCGA-DK-A1AE-01A-11D-A13W-08 TCGA-DK-A1AE-10A-01D-A13W-08 g.chr6:138192400G>C c.36G>C c.(34-36)ttG>ttC p.L12F BLCA 6 138196119 138196119 + Missense_Mutation SNP G G C TCGA-4Z-AA7M-01A-11D-A391-08 TCGA-4Z-AA7M-10A-01D-A394-08 g.chr6:138196119G>C c.433G>C c.(433-435)Gag>Cag p.E145Q BLCA 6 138196146 138196146 + Missense_Mutation SNP G G C TCGA-XF-A9T5-01A-11D-A42E-08 TCGA-XF-A9T5-10A-01D-A42H-08 g.chr6:138196146G>C c.460G>C c.(460-462)Gaa>Caa p.E154Q BLCA 6 138196164 138196164 + Missense_Mutation SNP G G A TCGA-UY-A78L-01A-12D-A339-08 TCGA-UY-A78L-10A-01D-A339-08 g.chr6:138196164G>A c.478G>A c.(478-480)Gat>Aat p.D160N BLCA 6 138198247 138198247 + Silent SNP G G A TCGA-G2-A2EK-01A-22D-A18F-08 TCGA-G2-A2EK-10A-01D-A18F-08 g.chr6:138198247G>A c.840G>A c.(838-840)cgG>cgA p.R280R BLCA 6 138198260 138198260 + Missense_Mutation SNP G G A TCGA-BT-A3PK-01A-21D-A21Z-08 TCGA-BT-A3PK-10A-01D-A21Z-08 g.chr6:138198260G>A c.853G>A c.(853-855)Gac>Aac p.D285N BLCA 6 138198296 138198296 + Missense_Mutation SNP G G A TCGA-ZF-A9R7-01A-11D-A38G-08 TCGA-ZF-A9R7-10A-01D-A38J-08 g.chr6:138198296G>A c.889G>A c.(889-891)Gag>Aag p.E297K BLCA 6 138199923 138199923 + Silent SNP G G A TCGA-CF-A5UA-01A-11D-A289-08 TCGA-CF-A5UA-10A-01D-A289-08 g.chr6:138199923G>A c.1341G>A c.(1339-1341)gcG>gcA p.A447A BLCA 6 138200359 138200359 + Missense_Mutation SNP C C G TCGA-ZF-AA4W-01A-12D-A38G-08 TCGA-ZF-AA4W-10A-01D-A38J-08 g.chr6:138200359C>G c.1777C>G c.(1777-1779)Caa>Gaa p.Q593E BRCA 6 138192623 138192623 + Nonsense_Mutation SNP C C T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr6:138192623C>T c.259C>T c.(259-261)Cga>Tga p.R87* BRCA 6 138196965 138196965 + Silent SNP C C G TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr6:138196965C>G c.627C>G c.(625-627)gtC>gtG p.V209V BRCA 6 138197148 138197148 + Missense_Mutation SNP G G C TCGA-AO-A1KR-01A-12D-A142-09 TCGA-AO-A1KR-10A-01D-A142-09 g.chr6:138197148G>C c.650G>C c.(649-651)aGt>aCt p.S217T BRCA 6 138198386 138198386 + Missense_Mutation SNP G G T TCGA-A2-A0YG-01A-21D-A10G-09 TCGA-A2-A0YG-10A-01D-A10G-09 g.chr6:138198386G>T c.979G>T c.(979-981)Gcc>Tcc p.A327S BRCA 6 138200082 138200082 + Silent SNP C C T TCGA-A2-A0EU-01A-22W-A071-09 TCGA-A2-A0EU-10A-01W-A071-09 g.chr6:138200082C>T c.1500C>T c.(1498-1500)aaC>aaT p.N500N BRCA 6 138201278 138201278 + Silent SNP G G T TCGA-AO-A0J4-01A-11W-A050-09 TCGA-AO-A0J4-10A-01W-A055-09 g.chr6:138201278G>T c.1977G>T c.(1975-1977)ggG>ggT p.G659G CESC 6 138192623 138192623 + Missense_Mutation SNP C C G TCGA-C5-A2M2-01A-21D-A18J-09 TCGA-C5-A2M2-10A-01D-A18J-09 g.chr6:138192623C>G c.259C>G c.(259-261)Cga>Gga p.R87G CESC 6 138196079 138196079 + Silent SNP G G A TCGA-IR-A3LA-01A-11D-A22X-09 TCGA-IR-A3LA-10A-01D-A22X-09 g.chr6:138196079G>A c.393G>A c.(391-393)aaG>aaA p.K131K CESC 6 138202276 138202276 + Missense_Mutation SNP G G T TCGA-DS-A7WF-01A-11D-A351-09 TCGA-DS-A7WF-10A-01D-A351-09 g.chr6:138202276G>T c.2193G>T c.(2191-2193)gaG>gaT p.E731D COAD 6 138192418 138192418 + Silent SNP T T C TCGA-CA-6716-01A-11D-1835-10 TCGA-CA-6716-10A-01D-1835-10 g.chr6:138192418T>C c.54T>C c.(52-54)gcT>gcC p.A18A COAD 6 138192457 138192457 + Silent SNP A A G TCGA-AY-5543-01A-01D-1650-10 TCGA-AY-5543-10A-01D-1650-10 g.chr6:138192457A>G c.93A>G c.(91-93)aaA>aaG p.K31K COAD 6 138192457 138192457 + Silent SNP A A G TCGA-CM-6170-01A-11D-1650-10 TCGA-CM-6170-10A-01D-1650-10 g.chr6:138192457A>G c.93A>G c.(91-93)aaA>aaG p.K31K COAD 6 138192457 138192457 + Silent SNP A A G TCGA-G4-6310-01A-11D-1719-10 TCGA-G4-6310-10A-01D-1720-10 g.chr6:138192457A>G c.93A>G c.(91-93)aaA>aaG p.K31K COAD 6 138192572 138192572 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr6:138192572G>A c.208G>A c.(208-210)Gac>Aac p.D70N COAD 6 138192618 138192618 + Missense_Mutation SNP G G C TCGA-D5-6929-01A-31D-1924-10 TCGA-D5-6929-10A-01D-1924-10 g.chr6:138192618G>C c.254G>C c.(253-255)tGg>tCg p.W85S COAD 6 138192632 138192632 + Missense_Mutation SNP C C T TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr6:138192632C>T c.268C>T c.(268-270)Cgg>Tgg p.R90W COAD 6 138195991 138195991 + Missense_Mutation SNP A A G TCGA-A6-6138-01A-11D-1771-10 TCGA-A6-6138-10A-01D-1771-10 g.chr6:138195991A>G c.305A>G c.(304-306)aAt>aGt p.N102S COAD 6 138196036 138196036 + Missense_Mutation SNP A A G TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr6:138196036A>G c.350A>G c.(349-351)gAc>gGc p.D117G COAD 6 138196036 138196036 + Missense_Mutation SNP A A G TCGA-CM-4744-01A-01D-1408-10 TCGA-CM-4744-10A-01D-1408-10 g.chr6:138196036A>G c.350A>G c.(349-351)gAc>gGc p.D117G COAD 6 138196036 138196036 + Missense_Mutation SNP A A G TCGA-CM-6169-01A-11D-1650-10 TCGA-CM-6169-10A-01D-1650-10 g.chr6:138196036A>G c.350A>G c.(349-351)gAc>gGc p.D117G COAD 6 138196109 138196109 + Silent SNP C C A TCGA-A6-5660-01A-01D-1650-10 TCGA-A6-5660-10A-01D-1650-10 g.chr6:138196109C>A c.423C>A c.(421-423)cgC>cgA p.R141R COAD 6 138196109 138196109 + Silent SNP C C T TCGA-AA-3496-01A-21D-1835-10 TCGA-AA-3496-11A-01D-1835-10 g.chr6:138196109C>T c.423C>T c.(421-423)cgC>cgT p.R141R COAD 6 138196111 138196111 + Nonsense_Mutation SNP G G A TCGA-G4-6299-01A-11D-1771-10 TCGA-G4-6299-10A-01D-1771-10 g.chr6:138196111G>A c.425G>A c.(424-426)tGg>tAg p.W142* COAD 6 138196149 138196149 + Missense_Mutation SNP A A G TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr6:138196149A>G c.463A>G c.(463-465)Acg>Gcg p.T155A COAD 6 138196149 138196149 + Missense_Mutation SNP A A G TCGA-AU-3779-01A-01D-1719-10 TCGA-AU-3779-10A-01D-1719-10 g.chr6:138196149A>G c.463A>G c.(463-465)Acg>Gcg p.T155A COAD 6 138196151 138196151 + Silent SNP G G A TCGA-AA-3660-01A-01D-1719-10 TCGA-AA-3660-11A-01D-1719-10 g.chr6:138196151G>A c.465G>A c.(463-465)acG>acA p.T155T COAD 6 138196151 138196151 + Silent SNP G G T TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr6:138196151G>T c.465G>T c.(463-465)acG>acT p.T155T COAD 6 138196856 138196856 + Missense_Mutation SNP A A C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr6:138196856A>C c.518A>C c.(517-519)aAa>aCa p.K173T COAD 6 138196886 138196886 + Missense_Mutation SNP G G A TCGA-AZ-5407-01A-01D-1719-10 TCGA-AZ-5407-10A-01D-1719-10 g.chr6:138196886G>A c.548G>A c.(547-549)cGa>cAa p.R183Q COAD 6 138196886 138196886 + Missense_Mutation SNP G G T TCGA-AZ-6599-01A-11D-1771-10 TCGA-AZ-6599-11A-01D-1771-10 g.chr6:138196886G>T c.548G>T c.(547-549)cGa>cTa p.R183L COAD 6 138196906 138196906 + Missense_Mutation SNP T T C TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr6:138196906T>C c.568T>C c.(568-570)Tca>Cca p.S190P COAD 6 138196907 138196907 + Missense_Mutation SNP C C T TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr6:138196907C>T c.569C>T c.(568-570)tCa>tTa p.S190L COAD 6 138197203 138197203 + Silent SNP T T C TCGA-A6-6141-01A-11D-1771-10 TCGA-A6-6141-10A-01D-1771-10 g.chr6:138197203T>C c.705T>C c.(703-705)ccT>ccC p.P235P COAD 6 138197203 138197203 + Silent SNP T T C TCGA-AY-6386-01A-21D-1719-10 TCGA-AY-6386-10A-01D-1719-10 g.chr6:138197203T>C c.705T>C c.(703-705)ccT>ccC p.P235P COAD 6 138198218 138198218 + Nonsense_Mutation SNP C C T TCGA-G4-6315-01A-11D-1719-10 TCGA-G4-6315-10A-01D-1720-10 g.chr6:138198218C>T c.811C>T c.(811-813)Cga>Tga p.R271* COAD 6 138198219 138198219 + Missense_Mutation SNP G G T TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr6:138198219G>T c.812G>T c.(811-813)cGa>cTa p.R271L COAD 6 138198220 138198220 + Silent SNP A A G TCGA-CM-6168-01A-11D-1650-10 TCGA-CM-6168-10A-01D-1650-10 g.chr6:138198220A>G c.813A>G c.(811-813)cgA>cgG p.R271R COAD 6 138198357 138198357 + Missense_Mutation SNP G G T TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr6:138198357G>T c.950G>T c.(949-951)tGg>tTg p.W317L COAD 6 138199567 138199567 + Splice_Site SNP A A G TCGA-CK-5914-01A-11D-1650-10 TCGA-CK-5914-10A-01D-1650-10 g.chr6:138199567A>G c.e7-1 COAD 6 138199577 138199578 + Missense_Mutation DNP AA AA GG TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr6:138199577_138199578AA>GG c.995_996AA>GG c.(994-996)gAA>gGG p.E332G COAD 6 138199578 138199578 + Silent SNP A A G TCGA-CM-5868-01A-01D-1650-10 TCGA-CM-5868-10A-01D-1650-10 g.chr6:138199578A>G c.996A>G c.(994-996)gaA>gaG p.E332E COAD 6 138199578 138199578 + Silent SNP A A G TCGA-DM-A0X9-01A-11D-A152-10 TCGA-DM-A0X9-10A-01D-A152-10 g.chr6:138199578A>G c.996A>G c.(994-996)gaA>gaG p.E332E COAD 6 138199587 138199587 + Silent SNP A A G TCGA-DM-A1DA-01A-11D-A152-10 TCGA-DM-A1DA-10A-01D-A152-10 g.chr6:138199587A>G c.1005A>G c.(1003-1005)ttA>ttG p.L335L COAD 6 138199647 138199647 + Silent SNP A A G TCGA-G4-6321-01A-11D-1719-10 TCGA-G4-6321-10A-01D-1720-10 g.chr6:138199647A>G c.1065A>G c.(1063-1065)aaA>aaG p.K355K COAD 6 138199648 138199648 + Missense_Mutation SNP T T C TCGA-D5-6537-01A-11D-1719-10 TCGA-D5-6537-10A-01D-1719-10 g.chr6:138199648T>C c.1066T>C c.(1066-1068)Tgg>Cgg p.W356R COAD 6 138199673 138199673 + Missense_Mutation SNP G G A TCGA-G4-6323-01A-11D-1719-10 TCGA-G4-6323-10A-01D-1720-10 g.chr6:138199673G>A c.1091G>A c.(1090-1092)aGg>aAg p.R364K COAD 6 138199712 138199712 + Missense_Mutation SNP T T C TCGA-DM-A28K-01A-21D-A16V-10 TCGA-DM-A28K-10A-01D-A16V-10 g.chr6:138199712T>C c.1130T>C c.(1129-1131)gTg>gCg p.V377A COAD 6 138199749 138199749 + Silent SNP G G A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr6:138199749G>A c.1167G>A c.(1165-1167)acG>acA p.T389T COAD 6 138199825 138199825 + Missense_Mutation SNP C C A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr6:138199825C>A c.1243C>A c.(1243-1245)Caa>Aaa p.Q415K COAD 6 138199856 138199856 + Missense_Mutation SNP C C T TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chr6:138199856C>T c.1274C>T c.(1273-1275)cCg>cTg p.P425L COAD 6 138199937 138199937 + Missense_Mutation SNP A A G TCGA-CK-4950-01A-01D-1719-10 TCGA-CK-4950-10A-01D-1719-10 g.chr6:138199937A>G c.1355A>G c.(1354-1356)gAg>gGg p.E452G COAD 6 138199944 138199945 + Frame_Shift_Ins INS - - G TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr6:138199944_138199945insG c.1362_1363insG c.(1363-1365)gggfs p.G455fs COAD 6 138199945 138199945 + Frame_Shift_Del DEL G G - TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr6:138199945delG c.1363delG c.(1363-1365)gggfs p.G456fs COAD 6 138200278 138200278 + Missense_Mutation SNP G G T TCGA-AA-3975-01A-01W-0995-10 TCGA-AA-3975-10A-01W-0999-10 g.chr6:138200278G>T c.1696G>T c.(1696-1698)Gat>Tat p.D566Y COAD 6 138200359 138200359 + Nonsense_Mutation SNP C C T TCGA-D5-6541-01A-11D-1719-10 TCGA-D5-6541-10A-01D-1719-10 g.chr6:138200359C>T c.1777C>T c.(1777-1779)Caa>Taa p.Q593* COAD 6 138201269 138201269 + Silent SNP G G A TCGA-D5-6538-01A-11D-1719-10 TCGA-D5-6538-10A-01D-1719-10 g.chr6:138201269G>A c.1968G>A c.(1966-1968)ccG>ccA p.P656P COAD 6 138201283 138201283 + Missense_Mutation SNP A A G TCGA-CK-4952-01A-01D-1719-10 TCGA-CK-4952-10A-01D-1719-10 g.chr6:138201283A>G c.1982A>G c.(1981-1983)gAa>gGa p.E661G COAD 6 138201284 138201284 + Silent SNP A A G TCGA-AZ-6600-01A-11D-1771-10 TCGA-AZ-6600-11A-01D-1771-10 g.chr6:138201284A>G c.1983A>G c.(1981-1983)gaA>gaG p.E661E COAD 6 138201335 138201335 + Missense_Mutation SNP C C A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr6:138201335C>A c.2034C>A c.(2032-2034)ttC>ttA p.F678L COAD 6 138202335 138202335 + Missense_Mutation SNP A A G TCGA-D5-6535-01A-11D-1719-10 TCGA-D5-6535-10A-01D-1719-10 g.chr6:138202335A>G c.2252A>G c.(2251-2253)gAg>gGg p.E751G COAD 6 138202398 138202398 + Missense_Mutation SNP A A G TCGA-D5-6536-01A-11D-1719-10 TCGA-D5-6536-10A-01D-1719-10 g.chr6:138202398A>G c.2315A>G c.(2314-2316)aAt>aGt p.N772S COAD 6 138202410 138202410 + Missense_Mutation SNP A A G TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr6:138202410A>G c.2327A>G c.(2326-2328)aAc>aGc p.N776S COAD 6 138202410 138202410 + Missense_Mutation SNP A A G TCGA-G4-6293-01A-11D-1719-10 TCGA-G4-6293-10A-01D-1719-10 g.chr6:138202410A>G c.2327A>G c.(2326-2328)aAc>aGc p.N776S COAD 6 138202411 138202411 + Silent SNP C C T TCGA-AA-3660-01A-01D-1719-10 TCGA-AA-3660-11A-01D-1719-10 g.chr6:138202411C>T c.2328C>T c.(2326-2328)aaC>aaT p.N776N COAD 6 138202424 138202424 + Nonsense_Mutation SNP G G T TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr6:138202424G>T c.2341G>T c.(2341-2343)Gaa>Taa p.E781* COAD 6 138202425 138202425 + Missense_Mutation SNP A A C TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr6:138202425A>C c.2342A>C c.(2341-2343)gAa>gCa p.E781A COAD 6 138202425 138202425 + Missense_Mutation SNP A A G TCGA-CK-4952-01A-01D-1719-10 TCGA-CK-4952-10A-01D-1719-10 g.chr6:138202425A>G c.2342A>G c.(2341-2343)gAa>gGa p.E781G COAD 6 138202426 138202426 + Silent SNP A A G TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr6:138202426A>G c.2343A>G c.(2341-2343)gaA>gaG p.E781E COADREAD 6 138192418 138192418 + Silent SNP T T C TCGA-CA-6716-01A-11D-1835-10 TCGA-CA-6716-10A-01D-1835-10 g.chr6:138192418T>C c.54T>C c.(52-54)gcT>gcC p.A18A COADREAD 6 138192457 138192457 + Silent SNP A A G TCGA-AY-5543-01A-01D-1650-10 TCGA-AY-5543-10A-01D-1650-10 g.chr6:138192457A>G c.93A>G c.(91-93)aaA>aaG p.K31K COADREAD 6 138192457 138192457 + Silent SNP A A G TCGA-CM-6170-01A-11D-1650-10 TCGA-CM-6170-10A-01D-1650-10 g.chr6:138192457A>G c.93A>G c.(91-93)aaA>aaG p.K31K COADREAD 6 138192457 138192457 + Silent SNP A A G TCGA-G4-6310-01A-11D-1719-10 TCGA-G4-6310-10A-01D-1720-10 g.chr6:138192457A>G c.93A>G c.(91-93)aaA>aaG p.K31K COADREAD 6 138192572 138192572 + Missense_Mutation SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr6:138192572G>A c.208G>A c.(208-210)Gac>Aac p.D70N COADREAD 6 138192618 138192618 + Missense_Mutation SNP G G C TCGA-D5-6929-01A-31D-1924-10 TCGA-D5-6929-10A-01D-1924-10 g.chr6:138192618G>C c.254G>C c.(253-255)tGg>tCg p.W85S COADREAD 6 138192632 138192632 + Missense_Mutation SNP C C T TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr6:138192632C>T c.268C>T c.(268-270)Cgg>Tgg p.R90W COADREAD 6 138195991 138195991 + Missense_Mutation SNP A A G TCGA-A6-6138-01A-11D-1771-10 TCGA-A6-6138-10A-01D-1771-10 g.chr6:138195991A>G c.305A>G c.(304-306)aAt>aGt p.N102S COADREAD 6 138196036 138196036 + Missense_Mutation SNP A A G TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr6:138196036A>G c.350A>G c.(349-351)gAc>gGc p.D117G COADREAD 6 138196036 138196036 + Missense_Mutation SNP A A G TCGA-CM-4744-01A-01D-1408-10 TCGA-CM-4744-10A-01D-1408-10 g.chr6:138196036A>G c.350A>G c.(349-351)gAc>gGc p.D117G COADREAD 6 138196036 138196036 + Missense_Mutation SNP A A G TCGA-CM-6169-01A-11D-1650-10 TCGA-CM-6169-10A-01D-1650-10 g.chr6:138196036A>G c.350A>G c.(349-351)gAc>gGc p.D117G COADREAD 6 138196109 138196109 + Silent SNP C C A TCGA-A6-5660-01A-01D-1650-10 TCGA-A6-5660-10A-01D-1650-10 g.chr6:138196109C>A c.423C>A c.(421-423)cgC>cgA p.R141R COADREAD 6 138196109 138196109 + Silent SNP C C T TCGA-AA-3496-01A-21D-1835-10 TCGA-AA-3496-11A-01D-1835-10 g.chr6:138196109C>T c.423C>T c.(421-423)cgC>cgT p.R141R COADREAD 6 138196111 138196111 + Nonsense_Mutation SNP G G A TCGA-G4-6299-01A-11D-1771-10 TCGA-G4-6299-10A-01D-1771-10 g.chr6:138196111G>A c.425G>A c.(424-426)tGg>tAg p.W142* COADREAD 6 138196149 138196149 + Missense_Mutation SNP A A G TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr6:138196149A>G c.463A>G c.(463-465)Acg>Gcg p.T155A COADREAD 6 138196149 138196149 + Missense_Mutation SNP A A G TCGA-AU-3779-01A-01D-1719-10 TCGA-AU-3779-10A-01D-1719-10 g.chr6:138196149A>G c.463A>G c.(463-465)Acg>Gcg p.T155A COADREAD 6 138196151 138196151 + Silent SNP G G A TCGA-AA-3660-01A-01D-1719-10 TCGA-AA-3660-11A-01D-1719-10 g.chr6:138196151G>A c.465G>A c.(463-465)acG>acA p.T155T COADREAD 6 138196151 138196151 + Silent SNP G G T TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr6:138196151G>T c.465G>T c.(463-465)acG>acT p.T155T COADREAD 6 138196856 138196856 + Missense_Mutation SNP A A C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr6:138196856A>C c.518A>C c.(517-519)aAa>aCa p.K173T COADREAD 6 138196886 138196886 + Missense_Mutation SNP G G A TCGA-AZ-5407-01A-01D-1719-10 TCGA-AZ-5407-10A-01D-1719-10 g.chr6:138196886G>A c.548G>A c.(547-549)cGa>cAa p.R183Q COADREAD 6 138196886 138196886 + Missense_Mutation SNP G G T TCGA-AZ-6599-01A-11D-1771-10 TCGA-AZ-6599-11A-01D-1771-10 g.chr6:138196886G>T c.548G>T c.(547-549)cGa>cTa p.R183L COADREAD 6 138196906 138196906 + Missense_Mutation SNP T T C TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr6:138196906T>C c.568T>C c.(568-570)Tca>Cca p.S190P COADREAD 6 138196907 138196907 + Missense_Mutation SNP C C T TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr6:138196907C>T c.569C>T c.(568-570)tCa>tTa p.S190L COADREAD 6 138197203 138197203 + Silent SNP T T C TCGA-A6-6141-01A-11D-1771-10 TCGA-A6-6141-10A-01D-1771-10 g.chr6:138197203T>C c.705T>C c.(703-705)ccT>ccC p.P235P COADREAD 6 138197203 138197203 + Silent SNP T T C TCGA-AY-6386-01A-21D-1719-10 TCGA-AY-6386-10A-01D-1719-10 g.chr6:138197203T>C c.705T>C c.(703-705)ccT>ccC p.P235P COADREAD 6 138198218 138198218 + Nonsense_Mutation SNP C C T TCGA-G4-6315-01A-11D-1719-10 TCGA-G4-6315-10A-01D-1720-10 g.chr6:138198218C>T c.811C>T c.(811-813)Cga>Tga p.R271* COADREAD 6 138198219 138198219 + Missense_Mutation SNP G G T TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr6:138198219G>T c.812G>T c.(811-813)cGa>cTa p.R271L COADREAD 6 138198220 138198220 + Silent SNP A A G TCGA-AG-3742-01A-11D-1657-10 TCGA-AG-3742-11A-01D-1657-10 g.chr6:138198220A>G c.813A>G c.(811-813)cgA>cgG p.R271R COADREAD 6 138198220 138198220 + Silent SNP A A G TCGA-CM-6168-01A-11D-1650-10 TCGA-CM-6168-10A-01D-1650-10 g.chr6:138198220A>G c.813A>G c.(811-813)cgA>cgG p.R271R COADREAD 6 138198312 138198312 + Missense_Mutation SNP T T C TCGA-DT-5265-01A-21D-1826-10 TCGA-DT-5265-10A-01D-1826-10 g.chr6:138198312T>C c.905T>C c.(904-906)cTc>cCc p.L302P COADREAD 6 138198357 138198357 + Missense_Mutation SNP G G T TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr6:138198357G>T c.950G>T c.(949-951)tGg>tTg p.W317L COADREAD 6 138199567 138199567 + Splice_Site SNP A A G TCGA-CK-5914-01A-11D-1650-10 TCGA-CK-5914-10A-01D-1650-10 g.chr6:138199567A>G c.e7-1 COADREAD 6 138199577 138199578 + Missense_Mutation DNP AA AA GG TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr6:138199577_138199578AA>GG c.995_996AA>GG c.(994-996)gAA>gGG p.E332G COADREAD 6 138199578 138199578 + Silent SNP A A G TCGA-CM-5868-01A-01D-1650-10 TCGA-CM-5868-10A-01D-1650-10 g.chr6:138199578A>G c.996A>G c.(994-996)gaA>gaG p.E332E COADREAD 6 138199578 138199578 + Silent SNP A A G TCGA-DM-A0X9-01A-11D-A152-10 TCGA-DM-A0X9-10A-01D-A152-10 g.chr6:138199578A>G c.996A>G c.(994-996)gaA>gaG p.E332E COADREAD 6 138199578 138199578 + Silent SNP A A G TCGA-DY-A1DC-01A-31D-A152-10 TCGA-DY-A1DC-10A-01D-A152-10 g.chr6:138199578A>G c.996A>G c.(994-996)gaA>gaG p.E332E COADREAD 6 138199587 138199587 + Silent SNP A A G TCGA-DM-A1DA-01A-11D-A152-10 TCGA-DM-A1DA-10A-01D-A152-10 g.chr6:138199587A>G c.1005A>G c.(1003-1005)ttA>ttG p.L335L COADREAD 6 138199647 138199647 + Silent SNP A A G TCGA-G4-6321-01A-11D-1719-10 TCGA-G4-6321-10A-01D-1720-10 g.chr6:138199647A>G c.1065A>G c.(1063-1065)aaA>aaG p.K355K COADREAD 6 138199648 138199648 + Missense_Mutation SNP T T C TCGA-D5-6537-01A-11D-1719-10 TCGA-D5-6537-10A-01D-1719-10 g.chr6:138199648T>C c.1066T>C c.(1066-1068)Tgg>Cgg p.W356R COADREAD 6 138199673 138199673 + Missense_Mutation SNP G G A TCGA-G4-6323-01A-11D-1719-10 TCGA-G4-6323-10A-01D-1720-10 g.chr6:138199673G>A c.1091G>A c.(1090-1092)aGg>aAg p.R364K COADREAD 6 138199712 138199712 + Missense_Mutation SNP T T C TCGA-DM-A28K-01A-21D-A16V-10 TCGA-DM-A28K-10A-01D-A16V-10 g.chr6:138199712T>C c.1130T>C c.(1129-1131)gTg>gCg p.V377A COADREAD 6 138199749 138199749 + Silent SNP G G A TCGA-AZ-6601-01A-11D-1771-10 TCGA-AZ-6601-11A-01D-1771-10 g.chr6:138199749G>A c.1167G>A c.(1165-1167)acG>acA p.T389T COADREAD 6 138199825 138199825 + Missense_Mutation SNP C C A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr6:138199825C>A c.1243C>A c.(1243-1245)Caa>Aaa p.Q415K COADREAD 6 138199856 138199856 + Missense_Mutation SNP C C T TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chr6:138199856C>T c.1274C>T c.(1273-1275)cCg>cTg p.P425L COADREAD 6 138199937 138199937 + Missense_Mutation SNP A A G TCGA-CK-4950-01A-01D-1719-10 TCGA-CK-4950-10A-01D-1719-10 g.chr6:138199937A>G c.1355A>G c.(1354-1356)gAg>gGg p.E452G COADREAD 6 138199944 138199945 + Frame_Shift_Ins INS - - G TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr6:138199944_138199945insG c.1362_1363insG c.(1363-1365)gggfs p.G455fs COADREAD 6 138199945 138199945 + Frame_Shift_Del DEL G G - TCGA-G4-6586-01A-11D-1771-10 TCGA-G4-6586-10A-01D-1771-10 g.chr6:138199945delG c.1363delG c.(1363-1365)gggfs p.G456fs COADREAD 6 138200278 138200278 + Missense_Mutation SNP G G T TCGA-AA-3975-01A-01W-0995-10 TCGA-AA-3975-10A-01W-0999-10 g.chr6:138200278G>T c.1696G>T c.(1696-1698)Gat>Tat p.D566Y COADREAD 6 138200292 138200292 + Silent SNP C C T TCGA-G5-6641-01A-11D-1826-10 TCGA-G5-6641-10A-01D-1826-10 g.chr6:138200292C>T c.1710C>T c.(1708-1710)ctC>ctT p.L570L COADREAD 6 138200294 138200294 + Missense_Mutation SNP T T C TCGA-AG-3732-01A-11D-1657-10 TCGA-AG-3732-11A-01D-1657-10 g.chr6:138200294T>C c.1712T>C c.(1711-1713)gTc>gCc p.V571A COADREAD 6 138200296 138200296 + Silent SNP C C A TCGA-G5-6641-01A-11D-1826-10 TCGA-G5-6641-10A-01D-1826-10 g.chr6:138200296C>A c.1714C>A c.(1714-1716)Cgg>Agg p.R572R COADREAD 6 138200345 138200345 + Missense_Mutation SNP C C G TCGA-AG-3609-01A-02W-0833-10 TCGA-AG-3609-10A-01W-0833-10 g.chr6:138200345C>G c.1763C>G c.(1762-1764)gCt>gGt p.A588G COADREAD 6 138200359 138200359 + Nonsense_Mutation SNP C C T TCGA-D5-6541-01A-11D-1719-10 TCGA-D5-6541-10A-01D-1719-10 g.chr6:138200359C>T c.1777C>T c.(1777-1779)Caa>Taa p.Q593* COADREAD 6 138201269 138201269 + Silent SNP G G A TCGA-D5-6538-01A-11D-1719-10 TCGA-D5-6538-10A-01D-1719-10 g.chr6:138201269G>A c.1968G>A c.(1966-1968)ccG>ccA p.P656P COADREAD 6 138201283 138201283 + Missense_Mutation SNP A A G TCGA-CK-4952-01A-01D-1719-10 TCGA-CK-4952-10A-01D-1719-10 g.chr6:138201283A>G c.1982A>G c.(1981-1983)gAa>gGa p.E661G COADREAD 6 138201284 138201284 + Silent SNP A A G TCGA-AZ-6600-01A-11D-1771-10 TCGA-AZ-6600-11A-01D-1771-10 g.chr6:138201284A>G c.1983A>G c.(1981-1983)gaA>gaG p.E661E COADREAD 6 138201335 138201335 + Missense_Mutation SNP C C A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr6:138201335C>A c.2034C>A c.(2032-2034)ttC>ttA p.F678L COADREAD 6 138202335 138202335 + Missense_Mutation SNP A A G TCGA-D5-6535-01A-11D-1719-10 TCGA-D5-6535-10A-01D-1719-10 g.chr6:138202335A>G c.2252A>G c.(2251-2253)gAg>gGg p.E751G COADREAD 6 138202398 138202398 + Missense_Mutation SNP A A G TCGA-D5-6536-01A-11D-1719-10 TCGA-D5-6536-10A-01D-1719-10 g.chr6:138202398A>G c.2315A>G c.(2314-2316)aAt>aGt p.N772S COADREAD 6 138202410 138202410 + Missense_Mutation SNP A A G TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr6:138202410A>G c.2327A>G c.(2326-2328)aAc>aGc p.N776S COADREAD 6 138202410 138202410 + Missense_Mutation SNP A A G TCGA-G4-6293-01A-11D-1719-10 TCGA-G4-6293-10A-01D-1719-10 g.chr6:138202410A>G c.2327A>G c.(2326-2328)aAc>aGc p.N776S COADREAD 6 138202411 138202411 + Silent SNP C C T TCGA-AA-3660-01A-01D-1719-10 TCGA-AA-3660-11A-01D-1719-10 g.chr6:138202411C>T c.2328C>T c.(2326-2328)aaC>aaT p.N776N COADREAD 6 138202424 138202424 + Nonsense_Mutation SNP G G T TCGA-DM-A1HB-01A-21D-A183-10 TCGA-DM-A1HB-10A-01D-A183-10 g.chr6:138202424G>T c.2341G>T c.(2341-2343)Gaa>Taa p.E781* COADREAD 6 138202425 138202425 + Missense_Mutation SNP A A C TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr6:138202425A>C c.2342A>C c.(2341-2343)gAa>gCa p.E781A COADREAD 6 138202425 138202425 + Missense_Mutation SNP A A G TCGA-CK-4952-01A-01D-1719-10 TCGA-CK-4952-10A-01D-1719-10 g.chr6:138202425A>G c.2342A>G c.(2341-2343)gAa>gGa p.E781G COADREAD 6 138202426 138202426 + Silent SNP A A G TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr6:138202426A>G c.2343A>G c.(2341-2343)gaA>gaG p.E781E DLBC 6 138192494 138192501 + Frame_Shift_Del DEL CACCGATA CACCGATA - TCGA-G8-6325-01A-11D-2210-10 TCGA-G8-6325-10A-01D-2210-10 g.chr6:138192494_138192501delCACCGATA c.130_137delCACCGATA c.(130-138)caccgatacfs p.HRY44fs DLBC 6 138192658 138192659 + Splice_Site INS - - GG TCGA-FF-A7CX-01A-12D-A382-10 TCGA-FF-A7CX-10A-01D-A385-10 g.chr6:138192658_138192659insGG c.294_295insGG c.(295-297)ggt>GGggt p.G99fs DLBC 6 138196066 138196066 + Missense_Mutation SNP T T G TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr6:138196066T>G c.380T>G c.(379-381)tTc>tGc p.F127C DLBC 6 138198239 138198240 + Frame_Shift_Del DEL AG AG - TCGA-FA-A86F-01A-11D-A382-10 TCGA-FA-A86F-10A-01D-A385-10 g.chr6:138198239_138198240delAG c.832_833delAG c.(832-834)agafs p.R278fs DLBC 6 138198372 138198376 + Frame_Shift_Del DEL CTCAT CTCAT - TCGA-FF-8041-01A-11D-2210-10 TCGA-FF-8041-10A-01D-2210-10 g.chr6:138198372_138198376delCTCAT c.965_969delCTCAT c.(964-969)actcatfs p.TH322fs DLBC 6 138200148 138200148 + Silent SNP A A G TCGA-GR-A4D5-01A-11D-A31X-10 TCGA-GR-A4D5-10A-01D-A31X-10 g.chr6:138200148A>G c.1566A>G c.(1564-1566)caA>caG p.Q522Q DLBC 6 138200319 138200319 + Nonsense_Mutation SNP C C A TCGA-GS-A9TZ-01A-11D-A38X-10 TCGA-GS-A9TZ-10A-01D-A38X-10 g.chr6:138200319C>A c.1737C>A c.(1735-1737)tgC>tgA p.C579* DLBC 6 138200459 138200460 + Frame_Shift_Del DEL TG TG - TCGA-FF-A7CR-01A-11D-A382-10 TCGA-FF-A7CR-10A-01D-A385-10 g.chr6:138200459_138200460delTG c.1877_1878delTG c.(1876-1878)ctgfs p.L626fs DLBC 6 138202395 138202395 + Missense_Mutation SNP G G A TCGA-GS-A9TZ-01A-11D-A38X-10 TCGA-GS-A9TZ-10A-01D-A38X-10 g.chr6:138202395G>A c.2312G>A c.(2311-2313)gGc>gAc p.G771D ESCA 6 138192616 138192616 + Missense_Mutation SNP C C G TCGA-L5-A8NI-01A-11D-A37C-09 TCGA-L5-A8NI-11A-11D-A37F-09 g.chr6:138192616C>G c.252C>G c.(250-252)aaC>aaG p.N84K ESCA 6 138196069 138196069 + Missense_Mutation SNP G G T TCGA-L5-A4OE-01A-11D-A27G-09 TCGA-L5-A4OE-11A-11D-A27G-09 g.chr6:138196069G>T c.383G>T c.(382-384)aGc>aTc p.S128I ESCA 6 138196886 138196886 + Missense_Mutation SNP G G T TCGA-L5-A8NV-01A-11D-A37C-09 TCGA-L5-A8NV-11A-11D-A37F-09 g.chr6:138196886G>T c.548G>T c.(547-549)cGa>cTa p.R183L ESCA 6 138197171 138197171 + Missense_Mutation SNP G G T TCGA-R6-A6XG-01B-11D-A33E-09 TCGA-R6-A6XG-10A-01D-A33H-09 g.chr6:138197171G>T c.673G>T c.(673-675)Gcc>Tcc p.A225S ESCA 6 138202351 138202351 + Frame_Shift_Del DEL C C - TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr6:138202351delC c.2268delC c.(2266-2268)gacfs p.D756fs GBMLGG 6 138195987 138195987 + Missense_Mutation SNP G G A TCGA-P5-A730-01A-11D-A32B-08 TCGA-P5-A730-10A-01D-A329-08 g.chr6:138195987G>A c.301G>A c.(301-303)Ggc>Agc p.G101S GBMLGG 6 138199814 138199814 + Missense_Mutation SNP G G A TCGA-DU-6401-01A-11D-1705-08 TCGA-DU-6401-10A-01D-1705-08 g.chr6:138199814G>A c.1232G>A c.(1231-1233)cGg>cAg p.R411Q GBMLGG 6 138201287 138201287 + Silent SNP C C T TCGA-HT-A61A-01A-11D-A29Q-08 TCGA-HT-A61A-10A-01D-A29Q-08 g.chr6:138201287C>T c.1986C>T c.(1984-1986)tgC>tgT p.C662C HNSC 6 138196092 138196092 + Missense_Mutation SNP C C T TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr6:138196092C>T c.406C>T c.(406-408)Cgc>Tgc p.R136C HNSC 6 138199945 138199945 + Frame_Shift_Del DEL G G - TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr6:138199945delG c.1363delG c.(1363-1365)gggfs p.G456fs HNSC 6 138200106 138200106 + Silent SNP C C T TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr6:138200106C>T c.1524C>T c.(1522-1524)caC>caT p.H508H HNSC 6 138200423 138200423 + Missense_Mutation SNP A A G TCGA-CN-4742-01A-02D-1512-08 TCGA-CN-4742-10A-01D-1512-08 g.chr6:138200423A>G c.1841A>G c.(1840-1842)tAt>tGt p.Y614C HNSC 6 138201248 138201248 + Silent SNP C C T TCGA-CQ-7071-01A-12D-A30E-08 TCGA-CQ-7071-10A-01D-A30H-08 g.chr6:138201248C>T c.1947C>T c.(1945-1947)tcC>tcT p.S649S HNSC 6 138202171 138202171 + Splice_Site SNP G G A TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr6:138202171G>A c.e9-1 HNSC 6 138202334 138202334 + Missense_Mutation SNP G G A TCGA-CR-6481-01A-11D-1870-08 TCGA-CR-6481-10A-01D-1870-08 g.chr6:138202334G>A c.2251G>A c.(2251-2253)Gag>Aag p.E751K HNSC 6 138202346 138202346 + Missense_Mutation SNP G G A TCGA-UF-A7JA-01A-12D-A34J-08 TCGA-UF-A7JA-10A-01D-A34M-08 g.chr6:138202346G>A c.2263G>A c.(2263-2265)Gaa>Aaa p.E755K KIPAN 6 138200108 138200108 + Missense_Mutation SNP C C T TCGA-DW-7841-01A-11D-2136-08 TCGA-DW-7841-10A-01D-2136-08 g.chr6:138200108C>T c.1526C>T c.(1525-1527)gCc>gTc p.A509V KIPAN 6 138200458 138200458 + Missense_Mutation SNP C C A TCGA-BQ-5890-01A-11D-1589-08 TCGA-BQ-5890-11A-01D-1589-08 g.chr6:138200458C>A c.1876C>A c.(1876-1878)Ctg>Atg p.L626M KIPAN 6 138201233 138201233 + Silent SNP C C T TCGA-CZ-5466-01A-01D-1501-10 TCGA-CZ-5466-11A-01D-1501-10 g.chr6:138201233C>T c.1932C>T c.(1930-1932)gtC>gtT p.V644V KIRC 6 138201233 138201233 + Silent SNP C C T TCGA-CZ-5466-01A-01D-1501-10 TCGA-CZ-5466-11A-01D-1501-10 g.chr6:138201233C>T c.1932C>T c.(1930-1932)gtC>gtT p.V644V KIRP 6 138200108 138200108 + Missense_Mutation SNP C C T TCGA-DW-7841-01A-11D-2136-08 TCGA-DW-7841-10A-01D-2136-08 g.chr6:138200108C>T c.1526C>T c.(1525-1527)gCc>gTc p.A509V KIRP 6 138200458 138200458 + Missense_Mutation SNP C C A TCGA-BQ-5890-01A-11D-1589-08 TCGA-BQ-5890-11A-01D-1589-08 g.chr6:138200458C>A c.1876C>A c.(1876-1878)Ctg>Atg p.L626M LGG 6 138195987 138195987 + Missense_Mutation SNP G G A TCGA-P5-A730-01A-11D-A32B-08 TCGA-P5-A730-10A-01D-A329-08 g.chr6:138195987G>A c.301G>A c.(301-303)Ggc>Agc p.G101S LGG 6 138199814 138199814 + Missense_Mutation SNP G G A TCGA-DU-6401-01A-11D-1705-08 TCGA-DU-6401-10A-01D-1705-08 g.chr6:138199814G>A c.1232G>A c.(1231-1233)cGg>cAg p.R411Q LGG 6 138201287 138201287 + Silent SNP C C T TCGA-HT-A61A-01A-11D-A29Q-08 TCGA-HT-A61A-10A-01D-A29Q-08 g.chr6:138201287C>T c.1986C>T c.(1984-1986)tgC>tgT p.C662C LIHC 6 138200242 138200242 + Missense_Mutation SNP A A G TCGA-G3-A3CJ-01A-11D-A20W-10 TCGA-G3-A3CJ-10A-01D-A20W-10 g.chr6:138200242A>G c.1660A>G c.(1660-1662)Agc>Ggc p.S554G LIHC 6 138202372 138202372 + Silent SNP G G T TCGA-LG-A9QD-01A-11D-A382-10 TCGA-LG-A9QD-10A-01D-A385-10 g.chr6:138202372G>T c.2289G>T c.(2287-2289)cgG>cgT p.R763R LUAD 6 138196953 138196953 + Missense_Mutation SNP G G T TCGA-MP-A4TH-01A-31D-A25L-08 TCGA-MP-A4TH-10A-01D-A25L-08 g.chr6:138196953G>T c.615G>T c.(613-615)agG>agT p.R205S LUAD 6 138199568 138199568 + Splice_Site SNP G G T TCGA-55-8301-01A-11D-2284-08 TCGA-55-8301-10A-01D-2284-08 g.chr6:138199568G>T c.e7-1 LUAD 6 138199659 138199659 + Missense_Mutation SNP C C A TCGA-05-4403-01A-01D-1265-08 TCGA-05-4403-10A-01D-1265-08 g.chr6:138199659C>A c.1077C>A c.(1075-1077)aaC>aaA p.N359K LUAD 6 138199845 138199845 + Silent SNP G G A TCGA-75-6214-01A-41D-1945-08 TCGA-75-6214-10A-01D-1946-08 g.chr6:138199845G>A c.1263G>A c.(1261-1263)ctG>ctA p.L421L LUAD 6 138199923 138199923 + Silent SNP G G T TCGA-05-4405-01A-21D-1855-08 TCGA-05-4405-10A-01D-1855-08 g.chr6:138199923G>T c.1341G>T c.(1339-1341)gcG>gcT p.A447A LUAD 6 138200479 138200479 + Missense_Mutation SNP G G A TCGA-78-7149-01A-11D-2036-08 TCGA-78-7149-10A-01D-2036-08 g.chr6:138200479G>A c.1897G>A c.(1897-1899)Gaa>Aaa p.E633K LUAD 6 138202269 138202269 + Missense_Mutation SNP G G A TCGA-86-A456-01A-11D-A24D-08 TCGA-86-A456-10A-01D-A24F-08 g.chr6:138202269G>A c.2186G>A c.(2185-2187)aGc>aAc p.S729N LUAD 6 138202310 138202310 + Missense_Mutation SNP A A T TCGA-L4-A4E5-01A-11D-A24P-08 TCGA-L4-A4E5-10A-01D-A24P-08 g.chr6:138202310A>T c.2227A>T c.(2227-2229)Atg>Ttg p.M743L LUSC 6 138192646 138192646 + Silent SNP G G C TCGA-39-5035-01A-01D-1441-08 TCGA-39-5035-11A-01D-1441-08 g.chr6:138192646G>C c.282G>C c.(280-282)gcG>gcC p.A94A LUSC 6 138196093 138196093 + Missense_Mutation SNP G G A TCGA-39-5030-01A-01D-1441-08 TCGA-39-5030-11A-01D-1441-08 g.chr6:138196093G>A c.407G>A c.(406-408)cGc>cAc p.R136H LUSC 6 138196127 138196127 + Silent SNP C C G TCGA-33-4532-01A-01D-1267-08 TCGA-33-4532-11A-01D-1267-08 g.chr6:138196127C>G c.441C>G c.(439-441)ctC>ctG p.L147L LUSC 6 138198379 138198379 + Silent SNP C C T TCGA-46-3769-01A-01D-0983-08 TCGA-46-3769-10A-01D-0983-08 g.chr6:138198379C>T c.972C>T c.(970-972)ctC>ctT p.L324L LUSC 6 138199982 138199982 + Missense_Mutation SNP C C A TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr6:138199982C>A c.1400C>A c.(1399-1401)cCt>cAt p.P467H LUSC 6 138200413 138200413 + Missense_Mutation SNP G G A TCGA-66-2734-01A-01D-0983-08 TCGA-66-2734-11A-01D-0983-08 g.chr6:138200413G>A c.1831G>A c.(1831-1833)Ggc>Agc p.G611S LUSC 6 138200446 138200446 + Missense_Mutation SNP G G T TCGA-60-2724-01A-01D-1522-08 TCGA-60-2724-11A-01D-1522-08 g.chr6:138200446G>T c.1864G>T c.(1864-1866)Ggc>Tgc p.G622C LUSC 6 138202416 138202416 + Missense_Mutation SNP A A G TCGA-66-2771-01A-01D-0983-08 TCGA-66-2771-11A-01D-0983-08 g.chr6:138202416A>G c.2333A>G c.(2332-2334)tAc>tGc p.Y778C OV 6 138192422 138192422 + Missense_Mutation SNP A A C TCGA-09-1669-01A-01W-0615-10 TCGA-09-1669-10A-01W-0616-10 g.chr6:138192422A>C c.58A>C c.(58-60)Aag>Cag p.K20Q OV 6 138195993 138195993 + Missense_Mutation SNP T T G TCGA-09-1661-01B-01W-0615-10 TCGA-09-1661-10A-01W-0616-10 g.chr6:138195993T>G c.307T>G c.(307-309)Tgc>Ggc p.C103G OV 6 138202410 138202410 + Missense_Mutation SNP A A G TCGA-13-0916-01A-01W-0420-08 TCGA-13-0916-10A-01D-0399-08 g.chr6:138202410A>G c.2327A>G c.(2326-2328)aAc>aGc p.N776S PAAD 6 138199962 138199962 + Silent SNP C C T TCGA-HZ-A8P0-01A-11D-A36O-08 TCGA-HZ-A8P0-10A-01D-A367-08 g.chr6:138199962C>T c.1380C>T c.(1378-1380)gcC>gcT p.A460A PAAD 6 138200249 138200249 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr6:138200249C>A c.1667C>A c.(1666-1668)cCt>cAt p.P556H PAAD 6 138202266 138202266 + Missense_Mutation SNP G G A TCGA-3A-A9I9-01A-11D-A38G-08 TCGA-3A-A9I9-10A-01D-A38J-08 g.chr6:138202266G>A c.2183G>A c.(2182-2184)cGc>cAc p.R728H PCPG 6 138201287 138201287 + Silent SNP C C T TCGA-RW-A684-01A-12D-A35D-08 TCGA-RW-A684-10A-01D-A35B-08 g.chr6:138201287C>T c.1986C>T c.(1984-1986)tgC>tgT p.C662C PRAD 6 138197133 138197133 + Splice_Site SNP A A G TCGA-G9-6494-01A-11D-1786-08 TCGA-G9-6494-10A-01D-1786-08 g.chr6:138197133A>G c.635A>G c.(634-636)gAc>gGc p.D212G READ 6 138198220 138198220 + Silent SNP A A G TCGA-AG-3742-01A-11D-1657-10 TCGA-AG-3742-11A-01D-1657-10 g.chr6:138198220A>G c.813A>G c.(811-813)cgA>cgG p.R271R READ 6 138198312 138198312 + Missense_Mutation SNP T T C TCGA-DT-5265-01A-21D-1826-10 TCGA-DT-5265-10A-01D-1826-10 g.chr6:138198312T>C c.905T>C c.(904-906)cTc>cCc p.L302P READ 6 138199578 138199578 + Silent SNP A A G TCGA-DY-A1DC-01A-31D-A152-10 TCGA-DY-A1DC-10A-01D-A152-10 g.chr6:138199578A>G c.996A>G c.(994-996)gaA>gaG p.E332E READ 6 138200292 138200292 + Silent SNP C C T TCGA-G5-6641-01A-11D-1826-10 TCGA-G5-6641-10A-01D-1826-10 g.chr6:138200292C>T c.1710C>T c.(1708-1710)ctC>ctT p.L570L READ 6 138200294 138200294 + Missense_Mutation SNP T T C TCGA-AG-3732-01A-11D-1657-10 TCGA-AG-3732-11A-01D-1657-10 g.chr6:138200294T>C c.1712T>C c.(1711-1713)gTc>gCc p.V571A READ 6 138200296 138200296 + Silent SNP C C A TCGA-G5-6641-01A-11D-1826-10 TCGA-G5-6641-10A-01D-1826-10 g.chr6:138200296C>A c.1714C>A c.(1714-1716)Cgg>Agg p.R572R READ 6 138200345 138200345 + Missense_Mutation SNP C C G TCGA-AG-3609-01A-02W-0833-10 TCGA-AG-3609-10A-01W-0833-10 g.chr6:138200345C>G c.1763C>G c.(1762-1764)gCt>gGt p.A588G SKCM 6 138192553 138192553 + Silent SNP C C T TCGA-FS-A1Z3-06A-11D-A197-08 TCGA-FS-A1Z3-10A-01D-A199-08 g.chr6:138192553C>T c.189C>T c.(187-189)atC>atT p.I63I SKCM 6 138196929 138196929 + Silent SNP T T C TCGA-ER-A2NC-06A-11D-A197-08 TCGA-ER-A2NC-10A-01D-A199-08 g.chr6:138196929T>C c.591T>C c.(589-591)ttT>ttC p.F197F SKCM 6 138197164 138197164 + Silent SNP C C T TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr6:138197164C>T c.666C>T c.(664-666)tcC>tcT p.S222S SKCM 6 138199917 138199917 + Silent SNP C C T TCGA-FS-A4F9-06A-11D-A24R-08 TCGA-FS-A4F9-10A-01D-A24R-08 g.chr6:138199917C>T c.1335C>T c.(1333-1335)ccC>ccT p.P445P SKCM 6 138200427 138200427 + Silent SNP T T C TCGA-OD-A75X-06A-12D-A32N-08 TCGA-OD-A75X-10A-01D-A32N-08 g.chr6:138200427T>C c.1845T>C c.(1843-1845)ttT>ttC p.F615F SKCM 6 138202199 138202199 + Nonsense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr6:138202199C>T c.2116C>T c.(2116-2118)Cga>Tga p.R706* SKCM 6 138202424 138202424 + Missense_Mutation SNP G G A TCGA-D3-A3MV-06A-11D-A21A-08 TCGA-D3-A3MV-10A-01D-A21A-08 g.chr6:138202424G>A c.2341G>A c.(2341-2343)Gaa>Aaa p.E781K

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-US 6 138192400 138192400 single base substitution G C missense_variant L12F 36G>C BLCA-US 6 138192400 138192400 single base substitution G C upstream_gene_variant BLCA-US 6 138198247 138198247 single base substitution G A downstream_gene_variant BLCA-US 6 138198247 138198247 single base substitution G A exon_variant BLCA-US 6 138198247 138198247 single base substitution G A synonymous_variant R280R 840G>A BLCA-US 6 138198260 138198260 single base substitution G A downstream_gene_variant BLCA-US 6 138198260 138198260 single base substitution G A exon_variant BLCA-US 6 138198260 138198260 single base substitution G A missense_variant D285N 853G>A BOCA-UK 6 138198329 138198329 single base substitution A G downstream_gene_variant BOCA-UK 6 138198329 138198329 single base substitution A G exon_variant BOCA-UK 6 138198329 138198329 single base substitution A G missense_variant M308V 922A>G BRCA-EU 6 138184406 138184406 single base substitution G A upstream_gene_variant BRCA-EU 6 138184605 138184605 single base substitution G C upstream_gene_variant BRCA-EU 6 138187932 138187932 single base substitution G A upstream_gene_variant BRCA-EU 6 138188050 138188050 single base substitution G C upstream_gene_variant BRCA-EU 6 138188817 138188817 single base substitution G C 5_prime_UTR_variant BRCA-EU 6 138188817 138188817 single base substitution G C intron_variant BRCA-EU 6 138190949 138190949 single base substitution G A intron_variant BRCA-EU 6 138191276 138191276 single base substitution C T intron_variant BRCA-EU 6 138192074 138192074 single base substitution G T intron_variant BRCA-EU 6 138192074 138192074 single base substitution G T upstream_gene_variant BRCA-EU 6 138192710 138192710 single base substitution G A downstream_gene_variant BRCA-EU 6 138192710 138192710 single base substitution G A intron_variant BRCA-EU 6 138192710 138192710 single base substitution G A upstream_gene_variant BRCA-EU 6 138192982 138192982 single base substitution C G downstream_gene_variant BRCA-EU 6 138192982 138192982 single base substitution C G intron_variant BRCA-EU 6 138192982 138192982 single base substitution C G upstream_gene_variant BRCA-EU 6 138195293 138195293 single base substitution C A downstream_gene_variant BRCA-EU 6 138195293 138195293 single base substitution C A intron_variant BRCA-EU 6 138195293 138195293 single base substitution C A upstream_gene_variant BRCA-EU 6 138196840 138196840 single base substitution T C downstream_gene_variant BRCA-EU 6 138196840 138196840 single base substitution T C missense_variant W168R 502T>C BRCA-EU 6 138196840 138196840 single base substitution T C upstream_gene_variant BRCA-EU 6 138198272 138198272 single base substitution C A downstream_gene_variant BRCA-EU 6 138198272 138198272 single base substitution C A exon_variant BRCA-EU 6 138198272 138198272 single base substitution C A missense_variant H289N 865C>A BRCA-EU 6 138198858 138198858 single base substitution A G downstream_gene_variant BRCA-EU 6 138198858 138198858 single base substitution A G intron_variant BRCA-EU 6 138199499 138199499 single base substitution A C downstream_gene_variant BRCA-EU 6 138199499 138199499 single base substitution A C intron_variant BRCA-EU 6 138199688 138199688 single base substitution C G downstream_gene_variant BRCA-EU 6 138199688 138199688 single base substitution C G missense_variant A369G 1106C>G BRCA-EU 6 138200678 138200678 single base substitution G A downstream_gene_variant BRCA-EU 6 138200678 138200678 single base substitution G A intron_variant BRCA-EU 6 138202345 138202345 single base substitution C T downstream_gene_variant BRCA-EU 6 138202345 138202345 single base substitution C T synonymous_variant P754P 2262C>T BRCA-EU 6 138205108 138205108 single base substitution G T downstream_gene_variant BRCA-EU 6 138205434 138205434 single base substitution T C downstream_gene_variant BRCA-EU 6 138206812 138206812 single base substitution G A downstream_gene_variant BRCA-EU 6 138207593 138207593 single base substitution A G downstream_gene_variant BRCA-EU 6 138208013 138208013 single base substitution G C downstream_gene_variant BRCA-EU 6 138208491 138208491 single base substitution T C downstream_gene_variant BRCA-EU 6 138208609 138208609 single base substitution C A downstream_gene_variant BRCA-EU 6 138208781 138208781 single base substitution G T downstream_gene_variant BRCA-EU 6 138208849 138208849 single base substitution G A downstream_gene_variant BRCA-EU 6 138209095 138209095 single base substitution C G downstream_gene_variant BRCA-EU 6 138209274 138209274 single base substitution C T downstream_gene_variant BRCA-EU 6 138209374 138209374 single base substitution C G downstream_gene_variant BRCA-FR 6 138191468 138191468 single base substitution C A intron_variant BRCA-FR 6 138206243 138206243 single base substitution G A downstream_gene_variant BRCA-FR 6 138206982 138206982 single base substitution C T downstream_gene_variant BRCA-US 6 138192623 138192623 single base substitution C T downstream_gene_variant BRCA-US 6 138192623 138192623 single base substitution C T stop_gained R87* 259C>T BRCA-US 6 138192623 138192623 single base substitution C T upstream_gene_variant BRCA-US 6 138196965 138196965 single base substitution C G downstream_gene_variant BRCA-US 6 138196965 138196965 single base substitution C G synonymous_variant V209V 627C>G BRCA-US 6 138196965 138196965 single base substitution C G upstream_gene_variant BRCA-US 6 138197148 138197148 single base substitution G C downstream_gene_variant BRCA-US 6 138197148 138197148 single base substitution G C exon_variant BRCA-US 6 138197148 138197148 single base substitution G C missense_variant S217T 650G>C BRCA-US 6 138198386 138198386 single base substitution G T downstream_gene_variant BRCA-US 6 138198386 138198386 single base substitution G T exon_variant BRCA-US 6 138198386 138198386 single base substitution G T missense_variant A327S 979G>T BRCA-US 6 138200082 138200082 single base substitution C T downstream_gene_variant BRCA-US 6 138200082 138200082 single base substitution C T synonymous_variant N500N 1500C>T BRCA-US 6 138201278 138201278 single base substitution G T downstream_gene_variant BRCA-US 6 138201278 138201278 single base substitution G T synonymous_variant G659G 1977G>T BTCA-JP 6 138192293 138192293 single base substitution G C intron_variant BTCA-JP 6 138192293 138192293 single base substitution G C upstream_gene_variant BTCA-JP 6 138192325 138192325 deletion of <=200bp T - intron_variant BTCA-JP 6 138192325 138192325 deletion of <=200bp T - upstream_gene_variant BTCA-JP 6 138196678 138196678 single base substitution G T downstream_gene_variant BTCA-JP 6 138196678 138196678 single base substitution G T intron_variant BTCA-JP 6 138196678 138196678 single base substitution G T upstream_gene_variant BTCA-JP 6 138196800 138196800 insertion of <=200bp - T downstream_gene_variant BTCA-JP 6 138196800 138196800 insertion of <=200bp - T intron_variant BTCA-JP 6 138196800 138196800 insertion of <=200bp - T upstream_gene_variant BTCA-JP 6 138199821 138199821 single base substitution G A downstream_gene_variant BTCA-JP 6 138199821 138199821 single base substitution G A synonymous_variant K413K 1239G>A BTCA-JP 6 138202346 138202346 single base substitution G A downstream_gene_variant BTCA-JP 6 138202346 138202346 single base substitution G A missense_variant E755K 2263G>A CESC-US 6 138192623 138192623 single base substitution C G downstream_gene_variant CESC-US 6 138192623 138192623 single base substitution C G missense_variant R87G 259C>G CESC-US 6 138192623 138192623 single base substitution C G upstream_gene_variant CESC-US 6 138196079 138196079 single base substitution G A downstream_gene_variant CESC-US 6 138196079 138196079 single base substitution G A synonymous_variant K131K 393G>A CESC-US 6 138196079 138196079 single base substitution G A upstream_gene_variant CESC-US 6 138202276 138202276 single base substitution G T downstream_gene_variant CESC-US 6 138202276 138202276 single base substitution G T missense_variant E731D 2193G>T CLLE-ES 6 138190849 138190849 single base substitution A C intron_variant CLLE-ES 6 138193126 138193126 single base substitution A C downstream_gene_variant CLLE-ES 6 138193126 138193126 single base substitution A C intron_variant CLLE-ES 6 138193126 138193126 single base substitution A C upstream_gene_variant CLLE-ES 6 138193477 138193477 single base substitution A G downstream_gene_variant CLLE-ES 6 138193477 138193477 single base substitution A G intron_variant CLLE-ES 6 138193477 138193477 single base substitution A G upstream_gene_variant CLLE-ES 6 138199301 138199301 single base substitution G C downstream_gene_variant CLLE-ES 6 138199301 138199301 single base substitution G C intron_variant COAD-US 6 138192572 138192572 single base substitution G A downstream_gene_variant COAD-US 6 138192572 138192572 single base substitution G A missense_variant D70N 208G>A COAD-US 6 138192572 138192572 single base substitution G A upstream_gene_variant COAD-US 6 138192632 138192632 single base substitution C T downstream_gene_variant COAD-US 6 138192632 138192632 single base substitution C T missense_variant R90W 268C>T COAD-US 6 138192632 138192632 single base substitution C T upstream_gene_variant COAD-US 6 138196856 138196856 single base substitution A C downstream_gene_variant COAD-US 6 138196856 138196856 single base substitution A C missense_variant K173T 518A>C COAD-US 6 138196856 138196856 single base substitution A C upstream_gene_variant COAD-US 6 138199749 138199749 single base substitution G A downstream_gene_variant COAD-US 6 138199749 138199749 single base substitution G A synonymous_variant T389T 1167G>A COAD-US 6 138199825 138199825 single base substitution C A downstream_gene_variant COAD-US 6 138199825 138199825 single base substitution C A missense_variant Q415K 1243C>A COAD-US 6 138199944 138199944 insertion of <=200bp - G downstream_gene_variant COAD-US 6 138199944 138199944 insertion of <=200bp - G frameshift_variant T454T? COAD-US 6 138199945 138199945 deletion of <=200bp G - downstream_gene_variant COAD-US 6 138199945 138199945 deletion of <=200bp G - frameshift_variant G455 COAD-US 6 138200453 138200453 single base substitution G A downstream_gene_variant COAD-US 6 138200453 138200453 single base substitution G A missense_variant C624Y 1871G>A COAD-US 6 138201266 138201266 single base substitution T A downstream_gene_variant COAD-US 6 138201266 138201266 single base substitution T A synonymous_variant I655I 1965T>A COAD-US 6 138201335 138201335 single base substitution C A downstream_gene_variant COAD-US 6 138201335 138201335 single base substitution C A missense_variant F678L 2034C>A COCA-CN 6 138192325 138192325 single base substitution T C intron_variant COCA-CN 6 138192325 138192325 single base substitution T C upstream_gene_variant COCA-CN 6 138197942 138197942 single base substitution A G downstream_gene_variant COCA-CN 6 138197942 138197942 single base substitution A G intron_variant COCA-CN 6 138200368 138200368 single base substitution C T downstream_gene_variant COCA-CN 6 138200368 138200368 single base substitution C T missense_variant R596W 1786C>T COCA-CN 6 138200418 138200418 single base substitution C T downstream_gene_variant COCA-CN 6 138200418 138200418 single base substitution C T synonymous_variant C612C 1836C>T ESAD-UK 6 138183546 138183546 single base substitution C T upstream_gene_variant ESAD-UK 6 138186640 138186640 single base substitution C T upstream_gene_variant ESAD-UK 6 138187682 138187682 single base substitution G T upstream_gene_variant ESAD-UK 6 138187684 138187684 single base substitution C T upstream_gene_variant ESAD-UK 6 138190184 138190184 single base substitution C G intron_variant ESAD-UK 6 138194255 138194257 deletion of <=200bp TTG - downstream_gene_variant ESAD-UK 6 138194255 138194257 deletion of <=200bp TTG - intron_variant ESAD-UK 6 138194255 138194257 deletion of <=200bp TTG - upstream_gene_variant ESAD-UK 6 138195987 138195987 single base substitution G A downstream_gene_variant ESAD-UK 6 138195987 138195987 single base substitution G A missense_variant G101S 301G>A ESAD-UK 6 138195987 138195987 single base substitution G A upstream_gene_variant ESAD-UK 6 138197696 138197696 single base substitution T G downstream_gene_variant ESAD-UK 6 138197696 138197696 single base substitution T G intron_variant ESAD-UK 6 138200571 138200571 single base substitution T C downstream_gene_variant ESAD-UK 6 138200571 138200571 single base substitution T C intron_variant ESAD-UK 6 138202050 138202050 single base substitution T G downstream_gene_variant ESAD-UK 6 138202050 138202050 single base substitution T G intron_variant ESAD-UK 6 138203228 138203228 single base substitution T C 3_prime_UTR_variant ESAD-UK 6 138203228 138203228 single base substitution T C downstream_gene_variant ESAD-UK 6 138205170 138205170 single base substitution C T downstream_gene_variant ESAD-UK 6 138205360 138205360 single base substitution C G downstream_gene_variant ESAD-UK 6 138205854 138205854 single base substitution A T downstream_gene_variant ESCA-CN 6 138198374 138198374 single base substitution C G downstream_gene_variant ESCA-CN 6 138198374 138198374 single base substitution C G exon_variant ESCA-CN 6 138198374 138198374 single base substitution C G missense_variant H323D 967C>G ESCA-CN 6 138201304 138201304 single base substitution C T downstream_gene_variant ESCA-CN 6 138201304 138201304 single base substitution C T missense_variant T668I 2003C>T GACA-CN 6 138197259 138197259 single base substitution G A downstream_gene_variant GACA-CN 6 138197259 138197259 single base substitution G A exon_variant GACA-CN 6 138197259 138197259 single base substitution G A missense_variant S254N 761G>A KIRC-US 6 138201233 138201233 single base substitution C T downstream_gene_variant KIRC-US 6 138201233 138201233 single base substitution C T synonymous_variant V644V 1932C>T KIRP-US 6 138200108 138200108 single base substitution C T downstream_gene_variant KIRP-US 6 138200108 138200108 single base substitution C T missense_variant A509V 1526C>T KIRP-US 6 138200458 138200458 single base substitution C A downstream_gene_variant KIRP-US 6 138200458 138200458 single base substitution C A missense_variant L626M 1876C>A LGG-US 6 138199814 138199814 single base substitution G A downstream_gene_variant LGG-US 6 138199814 138199814 single base substitution G A missense_variant R411Q 1232G>A LGG-US 6 138201287 138201287 single base substitution C T downstream_gene_variant LGG-US 6 138201287 138201287 single base substitution C T synonymous_variant C662C 1986C>T LICA-FR 6 138200419 138200419 single base substitution G A downstream_gene_variant LICA-FR 6 138200419 138200419 single base substitution G A missense_variant V613M 1837G>A LINC-JP 6 138190521 138190521 single base substitution C T intron_variant LINC-JP 6 138192617 138192617 single base substitution T A downstream_gene_variant LINC-JP 6 138192617 138192617 single base substitution T A missense_variant W85R 253T>A LINC-JP 6 138192617 138192617 single base substitution T A upstream_gene_variant LINC-JP 6 138199507 138199507 single base substitution A T downstream_gene_variant LINC-JP 6 138199507 138199507 single base substitution A T intron_variant LIRI-JP 6 138183700 138183700 single base substitution T C upstream_gene_variant LIRI-JP 6 138186996 138186996 single base substitution A G upstream_gene_variant LIRI-JP 6 138187724 138187724 single base substitution G A upstream_gene_variant LIRI-JP 6 138189390 138189390 single base substitution G A intron_variant LIRI-JP 6 138190521 138190521 single base substitution C T intron_variant LIRI-JP 6 138192525 138192525 single base substitution G A downstream_gene_variant LIRI-JP 6 138192525 138192525 single base substitution G A missense_variant C54Y 161G>A LIRI-JP 6 138192525 138192525 single base substitution G A upstream_gene_variant LIRI-JP 6 138196821 138196821 single base substitution T C downstream_gene_variant LIRI-JP 6 138196821 138196821 single base substitution T C splice_region_variant LIRI-JP 6 138196821 138196821 single base substitution T C upstream_gene_variant LIRI-JP 6 138197647 138197647 single base substitution A G downstream_gene_variant LIRI-JP 6 138197647 138197647 single base substitution A G intron_variant LIRI-JP 6 138199224 138199224 single base substitution T G downstream_gene_variant LIRI-JP 6 138199224 138199224 single base substitution T G intron_variant LIRI-JP 6 138199705 138199705 single base substitution C T downstream_gene_variant LIRI-JP 6 138199705 138199705 single base substitution C T missense_variant P375S 1123C>T LIRI-JP 6 138204277 138204277 single base substitution T A 3_prime_UTR_variant LIRI-JP 6 138204277 138204277 single base substitution T A downstream_gene_variant LUSC-KR 6 138183395 138183395 single base substitution C A upstream_gene_variant LUSC-KR 6 138186235 138186235 single base substitution G A upstream_gene_variant LUSC-KR 6 138187680 138187680 single base substitution G A upstream_gene_variant LUSC-KR 6 138187722 138187722 single base substitution A G upstream_gene_variant LUSC-KR 6 138190521 138190521 single base substitution C T intron_variant LUSC-KR 6 138192745 138192745 single base substitution G A downstream_gene_variant LUSC-KR 6 138192745 138192745 single base substitution G A intron_variant LUSC-KR 6 138192745 138192745 single base substitution G A upstream_gene_variant LUSC-KR 6 138194028 138194028 single base substitution G C downstream_gene_variant LUSC-KR 6 138194028 138194028 single base substitution G C intron_variant LUSC-KR 6 138194028 138194028 single base substitution G C upstream_gene_variant LUSC-KR 6 138196066 138196066 single base substitution T G downstream_gene_variant LUSC-KR 6 138196066 138196066 single base substitution T G missense_variant F127C 380T>G LUSC-KR 6 138196066 138196066 single base substitution T G upstream_gene_variant LUSC-KR 6 138196151 138196151 single base substitution G T downstream_gene_variant LUSC-KR 6 138196151 138196151 single base substitution G T synonymous_variant T155T 465G>T LUSC-KR 6 138196151 138196151 single base substitution G T upstream_gene_variant LUSC-KR 6 138197607 138197607 single base substitution G T downstream_gene_variant LUSC-KR 6 138197607 138197607 single base substitution G T intron_variant LUSC-KR 6 138198407 138198407 single base substitution G A downstream_gene_variant LUSC-KR 6 138198407 138198407 single base substitution G A intron_variant LUSC-KR 6 138202360 138202360 single base substitution G T downstream_gene_variant LUSC-KR 6 138202360 138202360 single base substitution G T missense_variant K759N 2277G>T LUSC-KR 6 138208227 138208227 single base substitution T C downstream_gene_variant LUSC-KR 6 138208429 138208429 single base substitution A G downstream_gene_variant LUSC-US 6 138192646 138192646 single base substitution G C downstream_gene_variant LUSC-US 6 138192646 138192646 single base substitution G C synonymous_variant A94A 282G>C LUSC-US 6 138192646 138192646 single base substitution G C upstream_gene_variant LUSC-US 6 138196093 138196093 single base substitution G A downstream_gene_variant LUSC-US 6 138196093 138196093 single base substitution G A missense_variant R136H 407G>A LUSC-US 6 138196093 138196093 single base substitution G A upstream_gene_variant LUSC-US 6 138196127 138196127 single base substitution C G downstream_gene_variant LUSC-US 6 138196127 138196127 single base substitution C G synonymous_variant L147L 441C>G LUSC-US 6 138196127 138196127 single base substitution C G upstream_gene_variant LUSC-US 6 138198379 138198379 single base substitution C T downstream_gene_variant LUSC-US 6 138198379 138198379 single base substitution C T exon_variant LUSC-US 6 138198379 138198379 single base substitution C T synonymous_variant L324L 972C>T LUSC-US 6 138199982 138199982 single base substitution C A downstream_gene_variant LUSC-US 6 138199982 138199982 single base substitution C A missense_variant P467H 1400C>A LUSC-US 6 138200413 138200413 single base substitution G A downstream_gene_variant LUSC-US 6 138200413 138200413 single base substitution G A missense_variant G611S 1831G>A LUSC-US 6 138200446 138200446 single base substitution G T downstream_gene_variant LUSC-US 6 138200446 138200446 single base substitution G T missense_variant G622C 1864G>T LUSC-US 6 138202416 138202416 single base substitution A G downstream_gene_variant LUSC-US 6 138202416 138202416 single base substitution A G missense_variant Y778C 2333A>G MALY-DE 6 138188684 138188685 deletion of <=200bp CC - intron_variant MALY-DE 6 138188684 138188685 deletion of <=200bp CC - upstream_gene_variant MALY-DE 6 138188851 138188851 single base substitution G A 5_prime_UTR_variant MALY-DE 6 138188851 138188851 single base substitution G A intron_variant MALY-DE 6 138188858 138188858 single base substitution G C 5_prime_UTR_variant MALY-DE 6 138188858 138188858 single base substitution G C intron_variant MALY-DE 6 138188912 138188912 single base substitution C T intron_variant MALY-DE 6 138188952 138188952 single base substitution G A intron_variant MALY-DE 6 138189001 138189001 single base substitution G A intron_variant MALY-DE 6 138189002 138189002 single base substitution C G intron_variant MALY-DE 6 138189029 138189029 single base substitution G A intron_variant MALY-DE 6 138189306 138189306 single base substitution G A intron_variant MALY-DE 6 138189324 138189324 single base substitution G C intron_variant MALY-DE 6 138189372 138189372 single base substitution G A intron_variant MALY-DE 6 138190050 138190050 single base substitution G A intron_variant MALY-DE 6 138190334 138190334 single base substitution C T intron_variant MALY-DE 6 138190597 138190597 single base substitution T G intron_variant MALY-DE 6 138192012 138192017 deletion of <=200bp TTGGTT - intron_variant MALY-DE 6 138192012 138192017 deletion of <=200bp TTGGTT - upstream_gene_variant MALY-DE 6 138192495 138192498 deletion of <=200bp ACCG - downstream_gene_variant MALY-DE 6 138192495 138192498 deletion of <=200bp ACCG - frameshift_variant HR44 MALY-DE 6 138192495 138192498 deletion of <=200bp ACCG - upstream_gene_variant MALY-DE 6 138192638 138192639 deletion of <=200bp CT - downstream_gene_variant MALY-DE 6 138192638 138192639 deletion of <=200bp CT - frameshift_variant L92 MALY-DE 6 138192638 138192639 deletion of <=200bp CT - upstream_gene_variant MALY-DE 6 138192660 138192660 single base substitution G T downstream_gene_variant MALY-DE 6 138192660 138192660 single base substitution G T splice_donor_variant MALY-DE 6 138192660 138192660 single base substitution G T upstream_gene_variant MALY-DE 6 138192661 138192661 single base substitution T G downstream_gene_variant MALY-DE 6 138192661 138192661 single base substitution T G splice_donor_variant MALY-DE 6 138192661 138192661 single base substitution T G upstream_gene_variant MALY-DE 6 138196058 138196058 insertion of <=200bp - G downstream_gene_variant MALY-DE 6 138196058 138196058 insertion of <=200bp - G frameshift_variant K124K? MALY-DE 6 138196058 138196058 insertion of <=200bp - G upstream_gene_variant MALY-DE 6 138198324 138198324 single base substitution A C downstream_gene_variant MALY-DE 6 138198324 138198324 single base substitution A C exon_variant MALY-DE 6 138198324 138198324 single base substitution A C missense_variant Y306S 917A>C MALY-DE 6 138202418 138202418 single base substitution T C downstream_gene_variant MALY-DE 6 138202418 138202418 single base substitution T C missense_variant C779R 2335T>C MALY-DE 6 138203281 138203281 single base substitution T A 3_prime_UTR_variant MALY-DE 6 138203281 138203281 single base substitution T A downstream_gene_variant MALY-DE 6 138203425 138203425 single base substitution T G 3_prime_UTR_variant MALY-DE 6 138203425 138203425 single base substitution T G downstream_gene_variant MALY-DE 6 138206339 138206339 single base substitution G A downstream_gene_variant MALY-DE 6 138206679 138206679 single base substitution C A downstream_gene_variant MALY-DE 6 138208467 138208469 deletion of <=200bp CTT - downstream_gene_variant MELA-AU 6 138184848 138184848 single base substitution C T upstream_gene_variant MELA-AU 6 138185218 138185218 single base substitution A G upstream_gene_variant MELA-AU 6 138185498 138185498 single base substitution C T upstream_gene_variant MELA-AU 6 138187778 138187778 single base substitution G A upstream_gene_variant MELA-AU 6 138188616 138188616 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 6 138188616 138188616 single base substitution C T upstream_gene_variant MELA-AU 6 138189585 138189585 single base substitution G A intron_variant MELA-AU 6 138190361 138190361 single base substitution C T intron_variant MELA-AU 6 138190470 138190470 single base substitution G A intron_variant MELA-AU 6 138190474 138190474 single base substitution A G intron_variant MELA-AU 6 138190521 138190521 single base substitution C T intron_variant MELA-AU 6 138190525 138190525 single base substitution C T intron_variant MELA-AU 6 138190869 138190869 single base substitution C T intron_variant MELA-AU 6 138190979 138190979 single base substitution C T intron_variant MELA-AU 6 138192341 138192341 single base substitution C T intron_variant MELA-AU 6 138192341 138192341 single base substitution C T upstream_gene_variant MELA-AU 6 138192353 138192353 single base substitution T C 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 6 138192353 138192353 single base substitution T C upstream_gene_variant MELA-AU 6 138193214 138193214 single base substitution G C downstream_gene_variant MELA-AU 6 138193214 138193214 single base substitution G C intron_variant MELA-AU 6 138193214 138193214 single base substitution G C upstream_gene_variant MELA-AU 6 138193487 138193487 single base substitution G A downstream_gene_variant MELA-AU 6 138193487 138193487 single base substitution G A intron_variant MELA-AU 6 138193487 138193487 single base substitution G A upstream_gene_variant MELA-AU 6 138194342 138194342 single base substitution C T downstream_gene_variant MELA-AU 6 138194342 138194342 single base substitution C T intron_variant MELA-AU 6 138194342 138194342 single base substitution C T upstream_gene_variant MELA-AU 6 138195142 138195142 single base substitution C T downstream_gene_variant MELA-AU 6 138195142 138195142 single base substitution C T intron_variant MELA-AU 6 138195142 138195142 single base substitution C T upstream_gene_variant MELA-AU 6 138195271 138195271 single base substitution C T downstream_gene_variant MELA-AU 6 138195271 138195271 single base substitution C T intron_variant MELA-AU 6 138195271 138195271 single base substitution C T upstream_gene_variant MELA-AU 6 138195977 138195977 single base substitution C T downstream_gene_variant MELA-AU 6 138195977 138195977 single base substitution C T intron_variant MELA-AU 6 138195977 138195977 single base substitution C T splice_region_variant MELA-AU 6 138195977 138195977 single base substitution C T upstream_gene_variant MELA-AU 6 138196638 138196638 single base substitution G A downstream_gene_variant MELA-AU 6 138196638 138196638 single base substitution G A intron_variant MELA-AU 6 138196638 138196638 single base substitution G A upstream_gene_variant MELA-AU 6 138197112 138197112 single base substitution C T downstream_gene_variant MELA-AU 6 138197112 138197112 single base substitution C T exon_variant MELA-AU 6 138197112 138197112 single base substitution C T intron_variant MELA-AU 6 138197482 138197482 single base substitution C T downstream_gene_variant MELA-AU 6 138197482 138197482 single base substitution C T intron_variant MELA-AU 6 138197814 138197814 single base substitution C T downstream_gene_variant MELA-AU 6 138197814 138197814 single base substitution C T intron_variant MELA-AU 6 138197989 138197989 single base substitution C T downstream_gene_variant MELA-AU 6 138197989 138197989 single base substitution C T intron_variant MELA-AU 6 138198042 138198042 single base substitution T A downstream_gene_variant MELA-AU 6 138198042 138198042 single base substitution T A intron_variant MELA-AU 6 138199295 138199295 single base substitution G C downstream_gene_variant MELA-AU 6 138199295 138199295 single base substitution G C intron_variant MELA-AU 6 138201267 138201267 single base substitution C T downstream_gene_variant MELA-AU 6 138201267 138201267 single base substitution C T missense_variant P656S 1966C>T MELA-AU 6 138201613 138201613 single base substitution A C downstream_gene_variant MELA-AU 6 138201613 138201613 single base substitution A C intron_variant MELA-AU 6 138204032 138204032 single base substitution T C 3_prime_UTR_variant MELA-AU 6 138204032 138204032 single base substitution T C downstream_gene_variant MELA-AU 6 138204035 138204035 single base substitution C T 3_prime_UTR_variant MELA-AU 6 138204035 138204035 single base substitution C T downstream_gene_variant MELA-AU 6 138204345 138204345 single base substitution C T 3_prime_UTR_variant MELA-AU 6 138204345 138204345 single base substitution C T downstream_gene_variant MELA-AU 6 138204999 138204999 single base substitution T C downstream_gene_variant MELA-AU 6 138207685 138207685 single base substitution A G downstream_gene_variant MELA-AU 6 138207828 138207828 single base substitution C T downstream_gene_variant MELA-AU 6 138207835 138207835 single base substitution G A downstream_gene_variant MELA-AU 6 138207918 138207918 single base substitution G A downstream_gene_variant MELA-AU 6 138208153 138208153 single base substitution C T downstream_gene_variant MELA-AU 6 138208596 138208596 single base substitution G A downstream_gene_variant MELA-AU 6 138208714 138208714 single base substitution G A downstream_gene_variant MELA-AU 6 138208939 138208939 single base substitution C T downstream_gene_variant MELA-AU 6 138209387 138209387 single base substitution C T downstream_gene_variant PACA-AU 6 138185121 138185121 single base substitution G A upstream_gene_variant PACA-AU 6 138191593 138191606 deletion of <=200bp TCCGGTGCGGAGGT - intron_variant PACA-AU 6 138200888 138200888 single base substitution C T downstream_gene_variant PACA-AU 6 138200888 138200888 single base substitution C T intron_variant PACA-AU 6 138202524 138202524 single base substitution C A 3_prime_UTR_variant PACA-AU 6 138202524 138202524 single base substitution C A downstream_gene_variant PACA-CA 6 138183854 138183854 single base substitution C A upstream_gene_variant PACA-CA 6 138187294 138187294 single base substitution C T upstream_gene_variant PACA-CA 6 138187648 138187648 single base substitution A C upstream_gene_variant PACA-CA 6 138191354 138191354 single base substitution A T intron_variant PACA-CA 6 138195747 138195747 single base substitution G A downstream_gene_variant PACA-CA 6 138195747 138195747 single base substitution G A intron_variant PACA-CA 6 138195747 138195747 single base substitution G A upstream_gene_variant PACA-CA 6 138196800 138196800 deletion of <=200bp T - downstream_gene_variant PACA-CA 6 138196800 138196800 deletion of <=200bp T - intron_variant PACA-CA 6 138196800 138196800 deletion of <=200bp T - upstream_gene_variant PACA-CA 6 138196819 138196819 single base substitution C A downstream_gene_variant PACA-CA 6 138196819 138196819 single base substitution C A splice_region_variant PACA-CA 6 138196819 138196819 single base substitution C A upstream_gene_variant PACA-CA 6 138201729 138201732 deletion of <=200bp GCCC - downstream_gene_variant PACA-CA 6 138201729 138201732 deletion of <=200bp GCCC - intron_variant PACA-CA 6 138201733 138201733 insertion of <=200bp - TA downstream_gene_variant PACA-CA 6 138201733 138201733 insertion of <=200bp - TA intron_variant PACA-CA 6 138207265 138207265 single base substitution G A downstream_gene_variant PACA-CA 6 138207875 138207875 single base substitution T G downstream_gene_variant PBCA-DE 6 138184004 138184004 deletion of <=200bp T - upstream_gene_variant PBCA-DE 6 138189598 138189598 insertion of <=200bp - T intron_variant PBCA-DE 6 138205447 138205447 deletion of <=200bp T - downstream_gene_variant PBCA-DE 6 138205447 138205447 insertion of <=200bp - T downstream_gene_variant PBCA-DE 6 138209442 138209442 deletion of <=200bp A - downstream_gene_variant PRAD-UK 6 138199923 138199923 single base substitution G A downstream_gene_variant PRAD-UK 6 138199923 138199923 single base substitution G A synonymous_variant A447A 1341G>A PRAD-UK 6 138200363 138200363 single base substitution C G downstream_gene_variant PRAD-UK 6 138200363 138200363 single base substitution C G missense_variant A594G 1781C>G PRAD-UK 6 138204511 138204511 single base substitution G C downstream_gene_variant PRAD-US 6 138197133 138197133 single base substitution A G downstream_gene_variant PRAD-US 6 138197133 138197133 single base substitution A G exon_variant PRAD-US 6 138197133 138197133 single base substitution A G missense_variant D212G 635A>G READ-US 6 138196093 138196093 single base substitution G A downstream_gene_variant READ-US 6 138196093 138196093 single base substitution G A missense_variant R136H 407G>A READ-US 6 138196093 138196093 single base substitution G A upstream_gene_variant READ-US 6 138200106 138200106 single base substitution C T downstream_gene_variant READ-US 6 138200106 138200106 single base substitution C T synonymous_variant H508H 1524C>T READ-US 6 138200292 138200292 single base substitution C T downstream_gene_variant READ-US 6 138200292 138200292 single base substitution C T synonymous_variant L570L 1710C>T READ-US 6 138200296 138200296 single base substitution C A downstream_gene_variant READ-US 6 138200296 138200296 single base substitution C A synonymous_variant R572R 1714C>A READ-US 6 138202424 138202424 single base substitution G A downstream_gene_variant READ-US 6 138202424 138202424 single base substitution G A missense_variant E781K 2341G>A RECA-EU 6 138197939 138197939 single base substitution C A downstream_gene_variant RECA-EU 6 138197939 138197939 single base substitution C A intron_variant RECA-EU 6 138202481 138202481 single base substitution G T 3_prime_UTR_variant RECA-EU 6 138202481 138202481 single base substitution G T downstream_gene_variant RECA-EU 6 138202482 138202482 single base substitution C T 3_prime_UTR_variant RECA-EU 6 138202482 138202482 single base substitution C T downstream_gene_variant RECA-EU 6 138205167 138205167 single base substitution C A downstream_gene_variant SKCA-BR 6 138186828 138186828 single base substitution G A upstream_gene_variant SKCA-BR 6 138188212 138188212 single base substitution C G upstream_gene_variant SKCA-BR 6 138190474 138190474 insertion of <=200bp - AGATG intron_variant SKCA-BR 6 138190509 138190533 deletion of <=200bp TGGATGGACGGACGGACGGACGGAC - intron_variant SKCA-BR 6 138190513 138190517 deletion of <=200bp TGGAC - intron_variant SKCA-BR 6 138195154 138195154 insertion of <=200bp - GA downstream_gene_variant SKCA-BR 6 138195154 138195154 insertion of <=200bp - GA intron_variant SKCA-BR 6 138195154 138195154 insertion of <=200bp - GA upstream_gene_variant SKCA-BR 6 138195901 138195901 single base substitution T C downstream_gene_variant SKCA-BR 6 138195901 138195901 single base substitution T C intron_variant SKCA-BR 6 138195901 138195901 single base substitution T C upstream_gene_variant SKCA-BR 6 138200808 138200808 single base substitution T C downstream_gene_variant SKCA-BR 6 138200808 138200808 single base substitution T C intron_variant SKCA-BR 6 138202350 138202350 single base substitution A C downstream_gene_variant SKCA-BR 6 138202350 138202350 single base substitution A C missense_variant D756A 2267A>C SKCA-BR 6 138202373 138202373 single base substitution G C downstream_gene_variant SKCA-BR 6 138202373 138202373 single base substitution G C missense_variant A764P 2290G>C SKCA-BR 6 138202783 138202783 single base substitution C T 3_prime_UTR_variant SKCA-BR 6 138202783 138202783 single base substitution C T downstream_gene_variant SKCA-BR 6 138202784 138202784 single base substitution C T 3_prime_UTR_variant SKCA-BR 6 138202784 138202784 single base substitution C T downstream_gene_variant SKCA-BR 6 138205063 138205063 single base substitution T G downstream_gene_variant SKCA-BR 6 138207349 138207349 single base substitution G A downstream_gene_variant SKCM-US 6 138192553 138192553 single base substitution C T downstream_gene_variant SKCM-US 6 138192553 138192553 single base substitution C T synonymous_variant I63I 189C>T SKCM-US 6 138192553 138192553 single base substitution C T upstream_gene_variant SKCM-US 6 138196929 138196929 single base substitution T C downstream_gene_variant SKCM-US 6 138196929 138196929 single base substitution T C synonymous_variant F197F 591T>C SKCM-US 6 138196929 138196929 single base substitution T C upstream_gene_variant SKCM-US 6 138197164 138197164 single base substitution C T downstream_gene_variant SKCM-US 6 138197164 138197164 single base substitution C T exon_variant SKCM-US 6 138197164 138197164 single base substitution C T synonymous_variant S222S 666C>T SKCM-US 6 138199917 138199917 single base substitution C T downstream_gene_variant SKCM-US 6 138199917 138199917 single base substitution C T synonymous_variant P445P 1335C>T SKCM-US 6 138202199 138202199 single base substitution C T downstream_gene_variant SKCM-US 6 138202199 138202199 single base substitution C T stop_gained R706* 2116C>T SKCM-US 6 138202424 138202424 single base substitution G A downstream_gene_variant SKCM-US 6 138202424 138202424 single base substitution G A missense_variant E781K 2341G>A STAD-US 6 138192409 138192409 single base substitution G T missense_variant M15I 45G>T STAD-US 6 138192409 138192409 single base substitution G T upstream_gene_variant STAD-US 6 138192545 138192545 single base substitution C T downstream_gene_variant STAD-US 6 138192545 138192545 single base substitution C T missense_variant R61W 181C>T STAD-US 6 138192545 138192545 single base substitution C T upstream_gene_variant STAD-US 6 138195987 138195987 single base substitution G A downstream_gene_variant STAD-US 6 138195987 138195987 single base substitution G A missense_variant G101S 301G>A STAD-US 6 138195987 138195987 single base substitution G A upstream_gene_variant STAD-US 6 138196150 138196150 single base substitution C T downstream_gene_variant STAD-US 6 138196150 138196150 single base substitution C T missense_variant T155M 464C>T STAD-US 6 138196150 138196150 single base substitution C T upstream_gene_variant STAD-US 6 138196151 138196151 single base substitution G A downstream_gene_variant STAD-US 6 138196151 138196151 single base substitution G A synonymous_variant T155T 465G>A STAD-US 6 138196151 138196151 single base substitution G A upstream_gene_variant STAD-US 6 138196897 138196897 single base substitution C T downstream_gene_variant STAD-US 6 138196897 138196897 single base substitution C T stop_gained Q187* 559C>T STAD-US 6 138196897 138196897 single base substitution C T upstream_gene_variant STAD-US 6 138197238 138197238 single base substitution C A downstream_gene_variant STAD-US 6 138197238 138197238 single base substitution C A exon_variant STAD-US 6 138197238 138197238 single base substitution C A missense_variant P247H 740C>A STAD-US 6 138199674 138199675 deletion of <=200bp GA - downstream_gene_variant STAD-US 6 138199674 138199675 deletion of <=200bp GA - frameshift_variant RR364 STAD-US 6 138199749 138199749 single base substitution G A downstream_gene_variant STAD-US 6 138199749 138199749 single base substitution G A synonymous_variant T389T 1167G>A STAD-US 6 138200209 138200209 single base substitution A G downstream_gene_variant STAD-US 6 138200209 138200209 single base substitution A G missense_variant T543A 1627A>G STAD-US 6 138200310 138200310 single base substitution G A downstream_gene_variant STAD-US 6 138200310 138200310 single base substitution G A synonymous_variant P576P 1728G>A STAD-US 6 138201244 138201244 single base substitution C T downstream_gene_variant STAD-US 6 138201244 138201244 single base substitution C T missense_variant A648V 1943C>T STAD-US 6 138201245 138201245 single base substitution G A downstream_gene_variant STAD-US 6 138201245 138201245 single base substitution G A synonymous_variant A648A 1944G>A STAD-US 6 138201287 138201287 single base substitution C T downstream_gene_variant STAD-US 6 138201287 138201287 single base substitution C T synonymous_variant C662C 1986C>T STAD-US 6 138202374 138202374 single base substitution C T downstream_gene_variant STAD-US 6 138202374 138202374 single base substitution C T missense_variant A764V 2291C>T UCEC-US 6 138196093 138196093 single base substitution G A downstream_gene_variant UCEC-US 6 138196093 138196093 single base substitution G A missense_variant R136H 407G>A UCEC-US 6 138196093 138196093 single base substitution G A upstream_gene_variant UCEC-US 6 138197171 138197171 single base substitution G A downstream_gene_variant UCEC-US 6 138197171 138197171 single base substitution G A exon_variant UCEC-US 6 138197171 138197171 single base substitution G A missense_variant A225T 673G>A UCEC-US 6 138199662 138199662 single base substitution C T downstream_gene_variant UCEC-US 6 138199662 138199662 single base substitution C T exon_variant UCEC-US 6 138199662 138199662 single base substitution C T synonymous_variant S360S 1080C>T UCEC-US 6 138199674 138199675 deletion of <=200bp GA - downstream_gene_variant UCEC-US 6 138199674 138199675 deletion of <=200bp GA - frameshift_variant RR364

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand 4 COSM35925 c.1004T>G p.L335* Substitution - Nonsense 6:137878449-137878449 + TCGA-B5-A11J-01 COSM1073799 c.1092_1093delGA p.E366fs*22 Deletion - Frameshift 6:137878537-137878538 + 1737775 COSM303672 c.559C>T p.Q187* Substitution - Nonsense 6:137875760-137875760 + 2318397 COSM3015736 c.2267_2268insC p.K759fs*10 Insertion - Frameshift 6:137881213-137881214 + 1604296 COSM133686 c.1246_1250delAACAA p.N416fs*11 Deletion - Frameshift 6:137878691-137878695 + TCGA-A2-A0EU-01 COSM450584 c.1500C>T p.N500N Substitution - coding silent 6:137878945-137878945 + 2089 COSM35949 c.52G>C p.A18P Substitution - Missense 6:137871279-137871279 + CSCC-49-T COSM4516631 c.2120_2121CC>TT p.T707I Substitution - Missense 6:137881066-137881067 + 13444 COSM303683 c.294_295insA p.G99fs*2 Insertion - Frameshift 6:137871521-137871522 + pfg008T COSM1642879 c.761G>T p.S254I Substitution - Missense 6:137876122-137876122 + 05-292 COSM36093 c.1_2373del2373 p.0? Whole gene deletion 6:137871228-137881319 + TCGA-09-1661-01 COSM115868 c.307T>G p.C103G Substitution - Missense 6:137874856-137874856 + 2217109 COSM4169397 c.? p.R702T Substitution - Missense HDLM-2 COSM36092 c.549_550ins29 p.S184fs*42 Insertion - Frameshift 6:137875750-137875751 + 2069 COSM36093 c.1_2373del2373 p.0? Whole gene deletion 6:137871228-137881319 + HCT15 COSM4632974 c.1423G>A p.A475T Substitution - Missense 6:137878868-137878868 + 1482139 COSM85877 c.106_107ins10 p.?fs Insertion - Frameshift 6:137871333-137871334 + EGC15 COSM87319 c.1756G>A p.A586T Substitution - Missense 6:137879201-137879201 + 21 COSM35916 c.1370delC p.P457fs*20 Deletion - Frameshift 6:137878815-137878815 + KM-H2 COSM36093 c.1_2373del2373 p.0? Whole gene deletion 6:137871228-137881319 + 3 COSM35928 c.2343A>T p.E781D Substitution - Missense 6:137881289-137881289 + 13460 COSM674142 c.989_989delT p.L330fs*13 Deletion - Frameshift 6:137878434-137878434 + TCGA-13-0916-01 COSM73029 c.2327A>G p.N776S Substitution - Missense 6:137881273-137881273 + PT34 COSM5910540 c.2305C>T p.H769Y Substitution - Missense 6:137881251-137881251 + 1960523 COSM1685345 c.? p.? Unknown ESCC_BICR_070T COSM5445089 c.967C>G p.H323D Substitution - Missense 6:137877237-137877237 + 13479 COSM674143 c.290_291insA p.N98fs*3 Insertion - Frameshift 6:137871517-137871518 + MALT055 COSM36093 c.1_2373del2373 p.0? Whole gene deletion 6:137871228-137881319 + CSCC-60-T COSM4506038 c.709C>T p.H237Y Substitution - Missense 6:137876070-137876070 + 11282 COSM110741 c.735_741delATACCCC p.Y246fs*14 Deletion - Frameshift 6:137876096-137876102 + T3498 COSM4734849 c.1786C>T p.R596W Substitution - Missense 6:137879231-137879231 + PM-3 COSM35978 c.811C>T p.R271* Substitution - Nonsense 6:137877081-137877081 + TCGA-HT-A61A-01 COSM3015726 c.1986C>T p.C662C Substitution - coding silent 6:137880150-137880150 + TCGA-46-3769-01 COSM739926 c.972C>T p.L324L Substitution - coding silent 6:137877242-137877242 + ATL334 COSM5709878 c.1166C>T p.T389M Substitution - Missense 6:137878611-137878611 + 1737800 COSM35921 c.971_975delTCATC p.L324fs*7 Deletion - Frameshift 6:137877241-137877245 + DLBCL028 COSM36093 c.1_2373del2373 p.0? Whole gene deletion 6:137871228-137881319 + 1482137 COSM85879 c.861_861delA p.V288fs*4 Deletion - Frameshift 6:137877131-137877131 + 1299335 COSM36249 c.305A>G p.N102S Substitution - Missense 6:137874854-137874854 + 1737797 COSM303693 c.491G>A p.W164* Substitution - Nonsense 6:137875692-137875692 + STC263 COSM1487264 c.1728G>A p.P576P Substitution - coding silent 6:137879173-137879173 + TCGA-18-3409-01 COSM739925 c.1400C>A p.P467H Substitution - Missense 6:137878845-137878845 + TCGA-FW-A3R5-06 COSM3920793 c.2116C>T p.R706* Substitution - Nonsense 6:137881062-137881062 + TCGA-G2-A2EK-01 COSM1311599 c.840G>A p.R280R Substitution - coding silent 6:137877110-137877110 + TCGA-AP-A051-01 COSM739928 c.407G>A p.R136H Substitution - Missense 6:137874956-137874956 + PD6750a COSM1637727 c.922A>G p.M308V Substitution - Missense 6:137877192-137877192 + MALT013 COSM35972 c.638_639insG p.M214fs*40 Insertion - Frameshift 6:137875999-137876000 + TCGA-CA-6717-01 COSM1440719 c.518A>C p.K173T Substitution - Missense 6:137875719-137875719 + 1737799 COSM303694 c.1485T>A p.C495* Substitution - Nonsense 6:137878930-137878930 + tumor_4120193 COSM3927952 c.2335T>C p.C779R Substitution - Missense 6:137881281-137881281 + TLE10 COSM4168108 c.2329G>T p.G777C Substitution - Missense 6:137881275-137881275 + HCC22T COSM1620959 c.253T>A p.W85R Substitution - Missense 6:137871480-137871480 + 1482135 COSM85872 c.1347_1423del77 p.P450fs*21 Deletion - Frameshift 6:137878792-137878868 + TCGA-EI-6917-01 COSM3430050 c.2341G>A p.E781K Substitution - Missense 6:137881287-137881287 + TCGA-FS-A4F9-06 COSM3621044 c.1335C>T p.P445P Substitution - coding silent 6:137878780-137878780 + 1737802 COSM303695 c.282_286delGCTGA p.L95fs*4 Deletion - Frameshift 6:137871509-137871513 + MALT087 COSM35979 c.2238_2239delGG p.A747fs*4 Deletion - Frameshift 6:137881184-137881185 + GHE0609 COSM35973 c.1877_1878delTG p.C627fs*44 Deletion - Frameshift 6:137879322-137879323 + 1737784 COSM303681 c.336_354del19 p.W113fs*4 Deletion - Frameshift 6:137874885-137874903 + SH-1362 COSM1685340 c.380T>G p.F127C Substitution - Missense 6:137874929-137874929 + GC1_T COSM150186 c.761G>A p.S254N Substitution - Missense 6:137876122-137876122 + 2318398 COSM4766049 c.506A>TT p.D169fs*85 Complex - frameshift 6:137875707-137875707 + SH-3133 COSM5019768 c.2364G>A p.M788I Substitution - Missense 6:137881310-137881310 + 2160 COSM35931 c.547C>T p.R183* Substitution - Nonsense 6:137875748-137875748 + 7-N COSM35957 c.866_867delAC p.H289fs*6 Deletion - Frameshift 6:137877136-137877137 + 1482143 COSM35978 c.811C>T p.R271* Substitution - Nonsense 6:137877081-137877081 + GHE0645 COSM5714694 c.315G>A p.M105I Substitution - Missense 6:137874864-137874864 + 9-C COSM36093 c.1_2373del2373 p.0? Whole gene deletion 6:137871228-137881319 + TCGA-AC-A23H-01 COSM3829147 c.627C>G p.V209V Substitution - coding silent 6:137875828-137875828 + HL21 COSM35969 c.503G>A p.W168* Substitution - Nonsense 6:137875704-137875704 + 25 COSM35920 c.1295_1296delGC p.G432fs*12 Deletion - Frameshift 6:137878740-137878741 + TCGA-D1-A103-01 COSM1073798 c.1080C>T p.S360S Substitution - coding silent 6:137878525-137878525 + 1960505 COSM1685340 c.380T>G p.F127C Substitution - Missense 6:137874929-137874929 + 587234 COSM1229861 c.1100G>T p.G367V Substitution - Missense 6:137878545-137878545 + TCGA-66-2734-01 COSM739924 c.1831G>A p.G611S Substitution - Missense 6:137879276-137879276 + TCGA-G4-6302-01 COSM3697535 c.1871G>A p.C624Y Substitution - Missense 6:137879316-137879316 + HL24 COSM35970 c.1421C>A p.T474N Substitution - Missense 6:137878866-137878866 + 1482142 COSM85881 c.295+1G>T p.? Unknown 6:137871523-137871523 + 1604308 COSM133692 c.400_401delGA p.D134fs*5 Deletion - Frameshift 6:137874949-137874950 + DOHH-2 COSM221037 c.1101G>A p.G367G Substitution - coding silent 6:137878546-137878546 + TCGA-AN-A046-01 COSM3829146 c.259C>T p.R87* Substitution - Nonsense 6:137871486-137871486 + SJRHB047 COSM3738165 c.1366G>C p.G456R Substitution - Missense 6:137878811-137878811 + SH-5693 COSM5020309 c.2295C>T p.P765P Substitution - coding silent 6:137881241-137881241 + RK066_C01 COSM1634521 c.1123C>T p.P375S Substitution - Missense 6:137878568-137878568 + 94699 COSM95374 c.1292C>T p.P431L Substitution - Missense 6:137878737-137878737 + 16 COSM35909 c.254G>A p.W85* Substitution - Nonsense 6:137871481-137871481 + 18 COSM35911 c.1354G>T p.E452* Substitution - Nonsense 6:137878799-137878799 + 11257 COSM43449 c.405_406delAC p.R136fs*3 Deletion - Frameshift 6:137874954-137874955 + L-1236 COSM35903 c.425G>A p.W142* Substitution - Nonsense 6:137874974-137874974 + 2186 COSM35931 c.547C>T p.R183* Substitution - Nonsense 6:137875748-137875748 + 1960501 COSM1685343 c.362_363ins136 p.Q150fs*35 Insertion - Frameshift 6:137874911-137874912 + 1296815 COSM36193 c.1777C>T p.Q593* Substitution - Nonsense 6:137879222-137879222 + 2015 COSM35941 c.994G>T p.E332* Substitution - Nonsense 6:137878439-137878439 + 3 COSM35926 c.322_323insA p.T108fs*32 Insertion - Frameshift 6:137874871-137874872 + GHE0609 COSM5713468 c.487-1_489delGAAC p.? Unknown 6:137875687-137875690 + C35 COSM87318 c.91A>T p.K31* Substitution - Nonsense 6:137871318-137871318 + 1774988 COSM169327 c.1763C>G p.A588G Substitution - Missense 6:137879208-137879208 + 1737798 COSM303900 c.733_733delA p.R245fs*17 Deletion - Frameshift 6:137876094-137876094 + ATL284 COSM5709879 c.1438_1439insGC p.P481fs*8 Insertion - Frameshift 6:137878883-137878884 + TCGA-CA-6718-01 COSM1440743 c.2034C>A p.F678L Substitution - Missense 6:137880198-137880198 + TCGA-09-1669-01 COSM119726 c.58A>C p.K20Q Substitution - Missense 6:137871285-137871285 + LUAD-E00918 COSM365360 c.2198G>T p.C733F Substitution - Missense 6:137881144-137881144 + SW48 COSM3015687 c.388C>A p.L130I Substitution - Missense 6:137874937-137874937 + 1482134 COSM85871 c.1880_1881delGT p.C627fs*44 Deletion - Frameshift 6:137879325-137879326 + T3306 COSM4734847 c.1412G>C p.S471T Substitution - Missense 6:137878857-137878857 + 22 COSM35917 c.745_751delGTTCTCG p.V249fs*11 Deletion - Frameshift 6:137876106-137876112 + PM-7 COSM5619662 c.241A>T p.K81* Substitution - Nonsense 6:137871468-137871468 + DLBCL-PatientA COSM220190 c.1316G>T p.R439L Substitution - Missense 6:137878761-137878761 + S02-14875-TP COSM4992436 c.1727C>T p.P576L Substitution - Missense 6:137879172-137879172 + TCGA-CA-6717-01 COSM1440736 c.1243C>A p.Q415K Substitution - Missense 6:137878688-137878688 + TCGA-DK-A1AE-01 COSM1311598 c.36G>C p.L12F Substitution - Missense 6:137871263-137871263 + TCGA-AD-6895-01 COSM1440713 c.268C>T p.R90W Substitution - Missense 6:137871495-137871495 + TCGA-DW-7841-01 COSM3994617 c.1526C>T p.A509V Substitution - Missense 6:137878971-137878971 + 4_FL COSM4171477 c.2109_2110delTG p.V704fs*47 Deletion - Frameshift 6:137881055-137881056 + 2089 COSM35948 c.7G>T p.E3* Substitution - Nonsense 6:137871234-137871234 + 1604297 COSM133688 c.553G>T p.G185* Substitution - Nonsense 6:137875754-137875754 + 1737791 COSM303688 c.1244_1248delAAAAC p.N416fs*11 Deletion - Frameshift 6:137878689-137878693 + YUROC COSM5404453 c.183G>A p.R61R Substitution - coding silent 6:137871410-137871410 + LUAD-74TBW COSM355275 c.222G>T p.Q74H Substitution - Missense 6:137871449-137871449 + 1737803 COSM303696 c.205_206insCCTC p.I69fs*33 Insertion - Frameshift 6:137871432-137871433 + DM16 COSM4465309 c.1376C>T p.S459L Substitution - Missense 6:137878821-137878821 + 2218480 COSM4169655 c.1141_1142insT p.S381fs*8 Insertion - Frameshift 6:137878586-137878587 + RDES COSM4586255 c.505G>A p.D169N Substitution - Missense 6:137875706-137875706 + 1355250 COSM43450 c.703C>A p.P235T Substitution - Missense 6:137876064-137876064 + TCGA-BR-4256-01 COSM3858566 c.464C>T p.T155M Substitution - Missense 6:137875013-137875013 + 44 COSM5762968 c.1178C>T p.P393L Substitution - Missense 6:137878623-137878623 + 2 COSM35908 c.2251G>A p.E751K Substitution - Missense 6:137881197-137881197 + PTC-28C COSM1685340 c.380T>G p.F127C Substitution - Missense 6:137874929-137874929 + 1774984 COSM36249 c.305A>G p.N102S Substitution - Missense 6:137874854-137874854 + 19 COSM35913 c.905T>C p.L302P Substitution - Missense 6:137877175-137877175 + HCC22 COSM1620959 c.253T>A p.W85R Substitution - Missense 6:137871480-137871480 + 1482135 COSM85873 c.1428G>A p.M476I Substitution - Missense 6:137878873-137878873 + 2176 COSM35946 c.1067G>A p.W356* Substitution - Nonsense 6:137878512-137878512 + TCGA-39-5035-01 COSM739929 c.282G>C p.A94A Substitution - coding silent 6:137871509-137871509 + DLBCL905 COSM1581846 c.615G>T p.R205S Substitution - Missense 6:137875816-137875816 + 11235 COSM110740 c.251_251delA p.N84fs*12 Deletion - Frameshift 6:137871478-137871478 + DLBCL923 COSM35937 c.1468C>T p.Q490* Substitution - Nonsense 6:137878913-137878913 + 1737783 COSM35925 c.1004T>G p.L335* Substitution - Nonsense 6:137878449-137878449 + NCI-H128 COSM23072 c.1129G>A p.V377M Substitution - Missense 6:137878574-137878574 + 1737787 COSM35937 c.1468C>T p.Q490* Substitution - Nonsense 6:137878913-137878913 + 1482146 COSM85870 c.1721C>T p.P574L Substitution - Missense 6:137879166-137879166 + TCGA-AZ-6601-01 COSM1440735 c.1167G>A p.T389T Substitution - coding silent 6:137878612-137878612 + HCT15 COSM3015724 c.1942G>T p.A648S Substitution - Missense 6:137880106-137880106 + RK122_C01 COSM3744940 c.161G>A p.C54Y Substitution - Missense 6:137871388-137871388 + 2036 COSM35944 c.987G>A p.K329K Substitution - coding silent 6:137878432-137878432 + 3 COSM36095 c.2371_2373TAA>CAG p.*791Q Nonstop extension 6:137881317-137881319 + 4 COSM3734917 c.328C>T p.Q110* Substitution - Nonsense 6:137874877-137874877 + 1 COSM35907 c.2209C>A p.Q737K Substitution - Missense 6:137881155-137881155 + MALT067 COSM36093 c.1_2373del2373 p.0? Whole gene deletion 6:137871228-137881319 + TCGA-60-2724-01 COSM739923 c.1864G>T p.G622C Substitution - Missense 6:137879309-137879309 + tumor_4147968 COSM5946907 c.372_373insG p.A125fs*15 Insertion - Frameshift 6:137874921-137874922 + 1737784 COSM303682 c.359T>G p.L120W Substitution - Missense 6:137874908-137874908 + HL23 COSM36284 c.? p.? Unknown C69 COSM36093 c.1_2373del2373 p.0? Whole gene deletion 6:137871228-137881319 + PD4965a COSM5778378 c.1106C>G p.A369G Substitution - Missense 6:137878551-137878551 + P08-2516 COSM247920 c.391A>C p.K131Q Substitution - Missense 6:137874940-137874940 + T2417 COSM4734848 c.1444G>A p.G482S Substitution - Missense 6:137878889-137878889 + GHE0609 COSM5713555 c.487-4_487-3insGTTC p.? Unknown 6:137875684-137875685 + 1299336 COSM36249 c.305A>G p.N102S Substitution - Missense 6:137874854-137874854 + TCGA-HU-A4GN-01 COSM1487264 c.1728G>A p.P576P Substitution - coding silent 6:137879173-137879173 + Karpas-1106P COSM35921 c.971_975delTCATC p.L324fs*7 Deletion - Frameshift 6:137877241-137877245 + 1737786 COSM35921 c.971_975delTCATC p.L324fs*7 Deletion - Frameshift 6:137877241-137877245 + LS180 COSM3015714 c.1685G>A p.R562H Substitution - Missense 6:137879130-137879130 + 6 COSM3734923 c.1681C>T p.Q561* Substitution - Nonsense 6:137879126-137879126 + 1355233 COSM43448 c.2273C>G p.P758R Substitution - Missense 6:137881219-137881219 + MALT051 COSM35973 c.1877_1878delTG p.C627fs*44 Deletion - Frameshift 6:137879322-137879323 + DLBCL807 COSM1581845 c.322A>G p.T108A Substitution - Missense 6:137874871-137874871 + 1960505 COSM1685341 c.382_382delA p.S128fs*88 Deletion - Frameshift 6:137874931-137874931 + 1604309 COSM133693 c.872_872delT p.L291fs*1 Deletion - Frameshift 6:137877142-137877142 + TCGA-BT-A3PK-01 COSM3777142 c.853G>A p.D285N Substitution - Missense 6:137877123-137877123 + TCGA-FP-A4BE-01 COSM3858564 c.181C>T p.R61W Substitution - Missense 6:137871408-137871408 + 2183 COSM35947 c.748_763del16 p.L250fs*7 Deletion - Frameshift 6:137876109-137876124 + 1737785 COSM303684 c.829_830insTGTT p.N277fs*9 Insertion - Frameshift 6:137877099-137877100 + MALT085 COSM35977 c.1368_1369insG p.P457fs*16 Insertion - Frameshift 6:137878813-137878814 + 1960505 COSM1685342 c.704_705delCT p.L236fs*17 Deletion - Frameshift 6:137876065-137876066 + 1604299 COSM133690 c.2266_2267insC p.D756fs*13 Insertion - Frameshift 6:137881212-137881213 + 2127 COSM36093 c.1_2373del2373 p.0? Whole gene deletion 6:137871228-137881319 + 2156 COSM35950 c.1981G>T p.E661* Substitution - Nonsense 6:137880145-137880145 + 1299337 COSM36250 c.1984_1988TGCGG>TTGCCGT p.C662fs*36 Complex - frameshift 6:137880148-137880152 + CSCC-31-T COSM1568055 c.1710C>T p.L570L Substitution - coding silent 6:137879155-137879155 + SU-DHL-2 COSM35931 c.547C>T p.R183* Substitution - Nonsense 6:137875748-137875748 + TCGA-HU-8602-01 COSM3858565 c.301G>A p.G101S Substitution - Missense 6:137874850-137874850 + NCI-H460 COSM1196932 c.406C>T p.R136C Substitution - Missense 6:137874955-137874955 + ATL314 COSM5709880 c.1616_1617insT p.F540fs*132 Insertion - Frameshift 6:137879061-137879062 + TCGA-13-1510-01 COSM120015 c.1261C>G p.L421V Substitution - Missense 6:137878706-137878706 + U-H01 COSM35904 c.127_134delATGCACCG p.M43fs*55 Deletion - Frameshift 6:137871354-137871361 + YUROG COSM5404454 c.595C>T p.L199F Substitution - Missense 6:137875796-137875796 + TCGA-ER-A193-06 COSM3621043 c.666C>T p.S222S Substitution - coding silent 6:137876027-137876027 + 17 COSM35910 c.1758_1809del52 p.P587fs*93 Deletion - Frameshift 6:137879203-137879254 + PTC-14C COSM4160225 c.295G>T p.G99C Substitution - Missense 6:137871522-137871522 + YUKLAB COSM1698078 c.1385C>A p.P462Q Substitution - Missense 6:137878830-137878830 + TCGA-DU-6401-01 COSM3928114 c.1232G>A p.R411Q Substitution - Missense 6:137878677-137878677 + DLBCL008 COSM36093 c.1_2373del2373 p.0? Whole gene deletion 6:137871228-137881319 + 2170 COSM36093 c.1_2373del2373 p.0? Whole gene deletion 6:137871228-137881319 + PTC-515C COSM4160226 c.1368G>A p.G456G Substitution - coding silent 6:137878813-137878813 + C27 COSM87317 c.262G>T p.E88* Substitution - Nonsense 6:137871489-137871489 + MALT053 COSM35974 c.950G>A p.W317* Substitution - Nonsense 6:137877220-137877220 + HL12 COSM35968 c.1090A>G p.R364G Substitution - Missense 6:137878535-137878535 + LPJ041 COSM1316040 c.1135C>T p.Q379* Substitution - Nonsense 6:137878580-137878580 + 1482137 COSM85880 c.294_295+4delCGGTAA p.? Unknown 6:137871521-137871526 + 1960506 COSM1685339 c.360_361insCTTG p.V121fs*20 Insertion - Frameshift 6:137874909-137874910 + CSCC-60-T COSM4555574 c.65G>A p.R22Q Substitution - Missense 6:137871292-137871292 + 1355249 COSM43449 c.405_406delAC p.R136fs*3 Deletion - Frameshift 6:137874954-137874955 + 107-212 COSM35945 c.1310_1319del10 p.A437fs*37 Deletion - Frameshift 6:137878755-137878764 + BD246T COSM5496148 c.1239G>A p.K413K Substitution - coding silent 6:137878684-137878684 + 24 COSM35919 c.1879_1880delTG p.C627fs*44 Deletion - Frameshift 6:137879324-137879325 + S01522 COSM4386841 c.735A>T p.R245S Substitution - Missense 6:137876096-137876096 + 1296817 COSM35978 c.811C>T p.R271* Substitution - Nonsense 6:137877081-137877081 + MALT086 COSM35978 c.811C>T p.R271* Substitution - Nonsense 6:137877081-137877081 + MALT054 COSM35975 c.436_437delTC p.L147fs*7 Deletion - Frameshift 6:137874985-137874986 + 11-C COSM35955 c.835_836delGA p.D279fs*5 Deletion - Frameshift 6:137877105-137877106 + 11280 COSM110742 c.788_789insG p.K264fs*6 Insertion - Frameshift 6:137876149-137876150 + DLD1 COSM3015724 c.1942G>T p.A648S Substitution - Missense 6:137880106-137880106 + tumor_4177376 COSM3357953 c.295+2T>G p.? Unknown 6:137871524-137871524 + 1737773 COSM36093 c.1_2373del2373 p.0? Whole gene deletion 6:137871228-137881319 + HL10 COSM35967 c.1711G>A p.V571I Substitution - Missense 6:137879156-137879156 + HX15T COSM1620959 c.253T>A p.W85R Substitution - Missense 6:137871480-137871480 + 6 COSM3734944 c.1343G>A p.W448* Substitution - Nonsense 6:137878788-137878788 + DLBCL695 COSM1581847 c.920T>A p.L307* Substitution - Nonsense 6:137877190-137877190 + 1482138 COSM85875 c.2290_2290delG p.A764fs*28 Deletion - Frameshift 6:137881236-137881236 + 1960525 COSM1685337 c.2254C>T p.P752S Substitution - Missense 6:137881200-137881200 + 1427995 COSM49065 c.295+43T>G p.? Unknown 6:137871565-137871565 + BK0092 COSM4188806 c.2368G>T p.G790C Substitution - Missense 6:137881314-137881314 + pfg008T COSM1642879 c.761G>T p.S254I Substitution - Missense 6:137876122-137876122 + 80 COSM5016163 c.1270delA p.K424fs*53 Deletion - Frameshift 6:137878715-137878715 + NCI-H1770 COSM23074 c.1967C>T p.P656L Substitution - Missense 6:137880131-137880131 + TCGA-G4-6302-01 COSM3697536 c.1965T>A p.I655I Substitution - coding silent 6:137880129-137880129 + Pat_59_B COSM5869404 c.1847G>A p.G616E Substitution - Missense 6:137879292-137879292 + LOVO COSM3015711 c.1476C>T p.N492N Substitution - coding silent 6:137878921-137878921 + 17-C COSM35958 c.301_303GGC>A p.G101fs*38 Complex - frameshift 6:137874850-137874852 + 1737782 COSM303679 c.581T>C p.I194T Substitution - Missense 6:137875782-137875782 + C79 COSM87319 c.1756G>A p.A586T Substitution - Missense 6:137879201-137879201 + 15002 COSM674140 c.1532_1533insC p.H512fs*22 Insertion - Frameshift 6:137878977-137878978 + TCGA-ER-A2NC-06 COSM3621042 c.591T>C p.F197F Substitution - coding silent 6:137875792-137875792 + TCGA-BQ-5890-01 COSM3994618 c.1876C>A p.L626M Substitution - Missense 6:137879321-137879321 + 07-215 COSM36093 c.1_2373del2373 p.0? Whole gene deletion 6:137871228-137881319 + 1427996 COSM49064 c.2175G>A p.L725L Substitution - coding silent 6:137881121-137881121 + 1737801 COSM303697 c.295+2_295+6delTAAGA p.? Unknown 6:137871524-137871528 + 23 COSM35918 c.926_927insT p.I310fs*23 Insertion - Frameshift 6:137877196-137877197 + 1737789 COSM303687 c.510_511insA p.L171fs*83 Insertion - Frameshift 6:137875711-137875712 + 1737783 COSM35921 c.971_975delTCATC p.L324fs*7 Deletion - Frameshift 6:137877241-137877245 + 2217108 COSM4169397 c.? p.R702T Substitution - Missense GHE0645 COSM5714695 c.728G>A p.C243Y Substitution - Missense 6:137876089-137876089 + HDLM2 COSM36092 c.549_550ins29 p.S184fs*42 Insertion - Frameshift 6:137875750-137875751 + 107-216 COSM35942 c.520_521delAT p.M174fs*79 Deletion - Frameshift 6:137875721-137875722 + 10-C COSM35953 c.1898_1899delAA p.N634fs*37 Deletion - Frameshift 6:137879343-137879344 + 1737794 COSM303675 c.1507C>T p.Q503* Substitution - Nonsense 6:137878952-137878952 + T1764 COSM1196932 c.406C>T p.R136C Substitution - Missense 6:137874955-137874955 + H460 COSM1196932 c.406C>T p.R136C Substitution - Missense 6:137874955-137874955 + TCGA-FS-A1Z3-06 COSM3621041 c.189C>T p.I63I Substitution - coding silent 6:137871416-137871416 + GHE0609 COSM36283 c.296-1G>A p.? Unknown 6:137874844-137874844 + TCGA-A6-5665-01 COSM1440738 c.1362_1363insG p.P457fs*16 Insertion - Frameshift 6:137878807-137878808 + HN_62995 COSM129796 c.1841A>G p.Y614C Substitution - Missense 6:137879286-137879286 + S07-39193-TP COSM4992435 c.1180delT p.F394fs*5 Deletion - Frameshift 6:137878625-137878625 + MALT047 COSM35980 c.2214_2215insT p.P739fs*13 Insertion - Frameshift 6:137881160-137881161 + RK308_C01 COSM3744941 c.487-4T>C p.? Unknown 6:137875684-137875684 + T10 COSM5345036 c.1101G>T p.G367G Substitution - coding silent 6:137878546-137878546 + DLBCL022 COSM36093 c.1_2373del2373 p.0? Whole gene deletion 6:137871228-137881319 + TCGA-EI-6882-01 COSM739928 c.407G>A p.R136H Substitution - Missense 6:137874956-137874956 + 1 COSM35922 c.1228_1229delAG p.R410fs*18 Deletion - Frameshift 6:137878673-137878674 + 11_FL COSM4171475 c.244A>T p.K82* Substitution - Nonsense 6:137871471-137871471 + TCGA-DS-A7WF-01 COSM4821637 c.2193G>T p.E731D Substitution - Missense 6:137881139-137881139 + S02277 COSM5683298 c.2146T>G p.C716G Substitution - Missense 6:137881092-137881092 + 1737795 COSM303691 c.838_848del11 p.R280fs*1 Deletion - Frameshift 6:137877108-137877118 + 21 COSM35915 c.149_155delTGTTCAG p.M50fs*44 Deletion - Frameshift 6:137871376-137871382 + 1737788 COSM303686 c.268_268delC p.R90fs*6 Deletion - Frameshift 6:137871495-137871495 + DLBCL998 COSM1582042 c.353_354delCA p.T118fs*21 Deletion - Frameshift 6:137874902-137874903 + 2149 COSM35951 c.2274_2275insC p.K759fs*10 Insertion - Frameshift 6:137881220-137881221 + DLBCL690 COSM1582017 c.872_873insT p.L291fs*5 Insertion - Frameshift 6:137877142-137877143 + BCM723T COSM4956388 c.1837G>A p.V613M Substitution - Missense 6:137879282-137879282 + 2318396 COSM4766048 c.130_137delCACCGATA p.R45fs*53 Deletion - Frameshift 6:137871357-137871364 + 2131 COSM35935 c.274delC p.V93fs*3 Deletion - Frameshift 6:137871501-137871501 + 10 COSM5762968 c.1178C>T p.P393L Substitution - Missense 6:137878623-137878623 + 2 COSM35930 c.569C>A p.S190* Substitution - Nonsense 6:137875770-137875770 + 1646012 COSM166296 c.? p.R271* Substitution - Nonsense TCGA-EI-6511-01 COSM3430049 c.1524C>T p.H508H Substitution - coding silent 6:137878969-137878969 + 1737790 COSM303687 c.510_511insA p.L171fs*83 Insertion - Frameshift 6:137875711-137875712 + 2463263 COSM5416028 c.? p.G221fs*? Frameshift MALT082 COSM36093 c.1_2373del2373 p.0? Whole gene deletion 6:137871228-137881319 + 1482141 COSM85881 c.295+1G>T p.? Unknown 6:137871523-137871523 + 2492729 COSM5727695 c.556C>T p.L186F Substitution - Missense 6:137875757-137875757 + tumor_4108992 COSM5949715 c.131_134delACCG p.R45fs*50 Deletion - Frameshift 6:137871358-137871361 + 13476 COSM957495 c.296-35_296-2del34 p.? Unknown 6:137874810-137874843 + LOVO COSM3015722 c.1867delT p.C624fs*73 Deletion - Frameshift 6:137879312-137879312 + TCGA-BR-4361-01 COSM3858568 c.1627A>G p.T543A Substitution - Missense 6:137879072-137879072 + 2463390 COSM5416030 c.1316G>C p.R439P Substitution - Missense 6:137878761-137878761 + 1960492 COSM1685338 c.295_295+4delGGTAA p.? Unknown 6:137871522-137871522 + TCGA-CG-5728-01 COSM3858569 c.1943C>T p.A648V Substitution - Missense 6:137880107-137880107 + DM1 COSM5610882 c.766C>T p.H256Y Substitution - Missense 6:137876127-137876127 + 1737774 COSM303671 c.733A>T p.R245* Substitution - Nonsense 6:137876094-137876094 + MALT066 COSM35976 c.1514_1515insA p.H505fs*29 Insertion - Frameshift 6:137878959-137878960 + TCGA-D7-8579-01 COSM303672 c.559C>T p.Q187* Substitution - Nonsense 6:137875760-137875760 + 1482145 COSM85869 c.350A>T p.D117V Substitution - Missense 6:137874899-137874899 + DLBCL1052 COSM1582016 c.771_772insTT p.V258fs*5 Insertion - Frameshift 6:137876132-137876133 + MALT042 COSM36093 c.1_2373del2373 p.0? Whole gene deletion 6:137871228-137881319 + 9691 COSM957496 c.2089-2_2089-1del2 p.? Unknown 6:137881033-137881034 + BCM723T COSM4956388 c.1837G>A p.V613M Substitution - Missense 6:137879282-137879282 + 1296820 COSM36194 c.460G>T p.E154* Substitution - Nonsense 6:137875009-137875009 + 010 COSM4169372 c.593T>C p.V198A Substitution - Missense 6:137875794-137875794 + 20_tFL COSM4171476 c.1806delG p.T604fs*93 Deletion - Frameshift 6:137879251-137879251 + PT37 COSM5919171 c.958G>A p.G320S Substitution - Missense 6:137877228-137877228 + ESCC_16 COSM5625863 c.392A>G p.K131R Substitution - Missense 6:137874941-137874941 + 1427994 COSM49065 c.295+43T>G p.? Unknown 6:137871565-137871565 + TCGA-C5-A2M2-01 COSM4837708 c.259C>G p.R87G Substitution - Missense 6:137871486-137871486 + 1737781 COSM303677 c.1367G>T p.G456V Substitution - Missense 6:137878812-137878812 + 1774987 COSM330660 c.1084C>T p.Q362* Substitution - Nonsense 6:137878529-137878529 + RKO COSM3015731 c.2102G>A p.R701H Substitution - Missense 6:137881048-137881048 + 20 COSM35914 c.2257G>A p.A753T Substitution - Missense 6:137881203-137881203 + MedB-1 COSM5622016 c.113A>G p.H38R Substitution - Missense 6:137871340-137871340 + 3 COSM35927 c.2316T>G p.N772K Substitution - Missense 6:137881262-137881262 + 1774989 COSM330661 c.1420A>G p.T474A Substitution - Missense 6:137878865-137878865 + 2161 COSM35952 c.255G>A p.W85* Substitution - Nonsense 6:137871482-137871482 + 1737777 COSM303674 c.1282G>T p.E428* Substitution - Nonsense 6:137878727-137878727 + 1737778 COSM36093 c.1_2373del2373 p.0? Whole gene deletion 6:137871228-137881319 + TCGA-AP-A051-01 COSM1073797 c.673G>A p.A225T Substitution - Missense 6:137876034-137876034 + MOLT-4 COSM1672797 c.1880G>A p.C627Y Substitution - Missense 6:137879325-137879325 + CSCC-44-T COSM4458957 c.1106C>T p.A369V Substitution - Missense 6:137878551-137878551 + ESCC_BICR_031T COSM5441115 c.2003C>T p.T668I Substitution - Missense 6:137880167-137880167 + 1296820 COSM36199 c.1876_1877delCT p.L626fs*45 Deletion - Frameshift 6:137879321-137879322 + 1737780 COSM303676 c.1309_1309delG p.A437fs*40 Deletion - Frameshift 6:137878754-137878754 + TCGA-AZ-4315-01 COSM1440711 c.208G>A p.D70N Substitution - Missense 6:137871435-137871435 + 2195 COSM35943 c.399_400delAG p.D134fs*5 Deletion - Frameshift 6:137874948-137874949 + BD6T COSM5498943 c.2263G>A p.E755K Substitution - Missense 6:137881209-137881209 + 2053 COSM36093 c.1_2373del2373 p.0? Whole gene deletion 6:137871228-137881319 + CHC322T COSM1685340 c.380T>G p.F127C Substitution - Missense 6:137874929-137874929 + 1604298 COSM133689 c.2209C>T p.Q737* Substitution - Nonsense 6:137881155-137881155 + 2063 COSM35939 c.162C>A p.C54* Substitution - Nonsense 6:137871389-137871389 + 1432961 COSM49165 c.465G>A p.T155T Substitution - coding silent 6:137875014-137875014 + CSCC-27-T COSM4465309 c.1376C>T p.S459L Substitution - Missense 6:137878821-137878821 + 1293252 COSM36097 c.2274_2275insCC p.K759fs*34 Insertion - Frameshift 6:137881220-137881221 + 2093 COSM35938 c.491_492insA p.W164fs*1 Insertion - Frameshift 6:137875692-137875693 + GHE1209 COSM1440738 c.1362_1363insG p.P457fs*16 Insertion - Frameshift 6:137878807-137878808 + SH-1439 COSM5021119 c.1062G>A p.K354K Substitution - coding silent 6:137878507-137878507 + DL-30 COSM35973 c.1877_1878delTG p.C627fs*44 Deletion - Frameshift 6:137879322-137879323 + 2011-2280:2012-366-T COSM1440739 c.1363delG p.P457fs*20 Deletion - Frameshift 6:137878808-137878808 + J33_T COSM1440718 c.465G>T p.T155T Substitution - coding silent 6:137875014-137875014 + 1737781 COSM303678 c.1368_1368delG p.P457fs*20 Deletion - Frameshift 6:137878813-137878813 + 2 COSM36094 c.1893_1906+7del21 p.? Unknown 6:137879338-137879358 + ATL038 COSM5709881 c.1664_1665insC p.P557fs*115 Insertion - Frameshift 6:137879109-137879110 + MALT084 COSM36093 c.1_2373del2373 p.0? Whole gene deletion 6:137871228-137881319 + 1482140 COSM85878 c.397_398insA p.T133fs*7 Insertion - Frameshift 6:137874946-137874947 + ATL005 COSM5709877 c.317_318insT p.A107fs*33 Insertion - Frameshift 6:137874866-137874867 + TP_2010 COSM5553727 c.2190G>A p.E730E Substitution - coding silent 6:137881136-137881136 + 1774990 COSM330662 c.1260_1260delG p.K420fs*2 Deletion - Frameshift 6:137878705-137878705 + TCGA-AO-A0J4-01 COSM450585 c.1977G>T p.G659G Substitution - coding silent 6:137880141-137880141 + 18-C COSM35954 c.1475_1476insA p.N492fs*5 Insertion - Frameshift 6:137878920-137878921 + 2318395 COSM4766047 c.1269_1270insC p.K424fs*5 Insertion - Frameshift 6:137878714-137878715 + PA285 COSM1163419 c.2149G>T p.A717S Substitution - Missense 6:137881095-137881095 + 1737779 COSM303675 c.1507C>T p.Q503* Substitution - Nonsense 6:137878952-137878952 + GHE0436 COSM35978 c.811C>T p.R271* Substitution - Nonsense 6:137877081-137877081 + TCGA-D7-A4YT-01 COSM3858563 c.45G>T p.M15I Substitution - Missense 6:137871272-137871272 + TCGA-BR-8487-01 COSM3858567 c.740C>A p.P247H Substitution - Missense 6:137876101-137876101 + 13460 COSM35921 c.971_975delTCATC p.L324fs*7 Deletion - Frameshift 6:137877241-137877245 + 2033 COSM35937 c.1468C>T p.Q490* Substitution - Nonsense 6:137878913-137878913 + Au3 COSM5602447 c.1792C>T p.P598S Substitution - Missense 6:137879237-137879237 + 1960527 COSM1685344 c.1875_1876delAC p.L626fs*45 Deletion - Frameshift 6:137879320-137879321 + Pat_41_B COSM5869403 c.539C>T p.P180L Substitution - Missense 6:137875740-137875740 + T3038 COSM4734846 c.1306G>A p.G436R Substitution - Missense 6:137878751-137878751 + 0078_CRUK_PC_0078_T1_DNA COSM4420782 c.1341G>A p.A447A Substitution - coding silent 6:137878786-137878786 + 1737776 COSM303673 c.1494C>A p.C498* Substitution - Nonsense 6:137878939-137878939 + 1737786 COSM303675 c.1507C>T p.Q503* Substitution - Nonsense 6:137878952-137878952 + MALT017 COSM36093 c.1_2373del2373 p.0? Whole gene deletion 6:137871228-137881319 + 2463391 COSM5416029 c.1525G>A p.A509T Substitution - Missense 6:137878970-137878970 + MALT008 COSM36093 c.1_2373del2373 p.0? Whole gene deletion 6:137871228-137881319 + RC-K8 COSM35933 c.2161delT p.C721fs*71 Deletion - Frameshift 6:137881107-137881107 + 1737796 COSM303692 c.406_407insA p.R136fs*4 Insertion - Frameshift 6:137874955-137874956 + PT53 COSM5941278 c.1114C>T p.P372S Substitution - Missense 6:137878559-137878559 + TCGA-HU-A4G8-01 COSM3858570 c.1944G>A p.A648A Substitution - coding silent 6:137880108-137880108 + TCGA-33-4532-01 COSM739927 c.441C>G p.L147L Substitution - coding silent 6:137874990-137874990 + TCGA-CZ-5466-01 COSM483461 c.1932C>T p.V644V Substitution - coding silent 6:137880096-137880096 + 2014 COSM35911 c.1354G>T p.E452* Substitution - Nonsense 6:137878799-137878799 + 2110 COSM36093 c.1_2373del2373 p.0? Whole gene deletion 6:137871228-137881319 + DLBCL016 COSM35971 c.262_263insA p.V89fs*12 Insertion - Frameshift 6:137871489-137871490 + 0004_CRUK_PC_0004_T1_DNA COSM5422499 c.1781C>G p.A594G Substitution - Missense 6:137879226-137879226 + SH-5693 COSM1685340 c.380T>G p.F127C Substitution - Missense 6:137874929-137874929 + SJBALL239_D COSM4994215 c.1868T>C p.F623S Substitution - Missense 6:137879313-137879313 + CSCC-55-T COSM4471551 c.1725C>T p.S575S Substitution - coding silent 6:137879170-137879170 + TCGA-G5-6641-01 COSM1568055 c.1710C>T p.L570L Substitution - coding silent 6:137879155-137879155 + TCGA-D3-A3MV-06 COSM3430050 c.2341G>A p.E781K Substitution - Missense 6:137881287-137881287 + CSCC-55-T COSM85870 c.1721C>T p.P574L Substitution - Missense 6:137879166-137879166 + SH-9771 COSM49064 c.2175G>A p.L725L Substitution - coding silent 6:137881121-137881121 + 1774986 COSM330660 c.1084C>T p.Q362* Substitution - Nonsense 6:137878529-137878529 + TCGA-HU-A4GQ-01 COSM3015726 c.1986C>T p.C662C Substitution - coding silent 6:137880150-137880150 + J30_T COSM3948073 c.2277G>T p.K759N Substitution - Missense 6:137881223-137881223 + 1482136 COSM85874 c.373_382del10 p.L126fs*87 Deletion - Frameshift 6:137874922-137874931 + TCGA-F1-6874-01 COSM49165 c.465G>A p.T155T Substitution - coding silent 6:137875014-137875014 + TCGA-A2-A0YG-01 COSM450583 c.979G>T p.A327S Substitution - Missense 6:137877249-137877249 + MALT014 COSM36283 c.296-1G>A p.? Unknown 6:137874844-137874844 + 15003 COSM674141 c.257_257delG p.C86fs*10 Deletion - Frameshift 6:137871484-137871484 + 10886 COSM36093 c.1_2373del2373 p.0? Whole gene deletion 6:137871228-137881319 + 19 COSM35912 c.66_67delGG p.R24fs*7 Deletion - Frameshift 6:137871293-137871294 + MO_1012 COSM1073797 c.673G>A p.A225T Substitution - Missense 6:137876034-137876034 + DM28 COSM5610883 c.1295G>T p.G432V Substitution - Missense 6:137878740-137878740 + Pat_45_B COSM5869402 c.446C>T p.S149F Substitution - Missense 6:137874995-137874995 + TCGA-G4-6586-01 COSM1440739 c.1363delG p.P457fs*20 Deletion - Frameshift 6:137878808-137878808 + 14-RS COSM1731955 c.1376C>G p.S459W Substitution - Missense 6:137878821-137878821 + MALT036 COSM36091 c.987-53_1048del115 p.? Unknown 6:137878379-137878493 + MD-343 COSM303419 c.750C>T p.L250L Substitution - coding silent 6:137876111-137876111 + MCL008 COSM36093 c.1_2373del2373 p.0? Whole gene deletion 6:137871228-137881319 + 1737793 COSM303690 c.1517_1536del20 p.A506fs*21 Deletion - Frameshift 6:137878962-137878981 + TCGA-G5-6641-01 COSM1568053 c.1714C>A p.R572R Substitution - coding silent 6:137879159-137879159 + TCGA-AA-3975-01 COSM297488 c.1696G>T p.D566Y Substitution - Missense 6:137879141-137879141 + 1737782 COSM303680 c.825_825delT p.V276fs*11 Deletion - Frameshift 6:137877095-137877095 + 2188 COSM35943 c.399_400delAG p.D134fs*5 Deletion - Frameshift 6:137874948-137874949 + 1646004 COSM166295 c.? p.Q503* Substitution - Nonsense TCGA-BR-6852-01 COSM3858571 c.2291C>T p.A764V Substitution - Missense 6:137881237-137881237 + 2318394 COSM4766046 c.1162G>T p.E388* Substitution - Nonsense 6:137878607-137878607 + PT51 COSM36193 c.1777C>T p.Q593* Substitution - Nonsense 6:137879222-137879222 + TCGA-G9-6494-01 COSM1132027 c.635A>G p.D212G Substitution - Missense 6:137875996-137875996 + 2186 COSM35934 c.285_286insA p.T97fs*4 Insertion - Frameshift 6:137871512-137871513 + pfg145T COSM4761835 c.133C>T p.R45* Substitution - Nonsense 6:137871360-137871360 + 2209 COSM144480 c.295+1_295+5delGTAAG p.? Unknown 6:137871523-137871527 + KM-H2 COSM35906 c.?_?del? p.? Unknown ESO-963 COSM1268201 c.637A>C p.K213Q Substitution - Missense 6:137875998-137875998 + 1736199 COSM303669 c.2274_2274delC p.K759fs*33 Deletion - Frameshift 6:137881220-137881220 + 1355249 COSM35955 c.835_836delGA p.D279fs*5 Deletion - Frameshift 6:137877105-137877106 + 3-C COSM35956 c.485delG p.N163fs*53 Deletion - Frameshift 6:137875034-137875034 + TCGA-AO-A1KR-01 COSM1487263 c.650G>C p.S217T Substitution - Missense 6:137876011-137876011 + TCGA-IR-A3LA-01 COSM4845526 c.393G>A p.K131K Substitution - coding silent 6:137874942-137874942 + 1737785 COSM303683 c.294_295insA p.G99fs*2 Insertion - Frameshift 6:137871521-137871522 + TCGA-66-2771-01 COSM739922 c.2333A>G p.Y778C Substitution - Missense 6:137881279-137881279 + FL024 COSM36093 c.1_2373del2373 p.0? Whole gene deletion 6:137871228-137881319 + TCGA-39-5030-01 COSM739928 c.407G>A p.R136H Substitution - Missense 6:137874956-137874956 + LS174T COSM3015714 c.1685G>A p.R562H Substitution - Missense 6:137879130-137879130 + 1737787 COSM303685 c.337_420del84 p.W113_F140del Deletion - In frame 6:137874886-137874969 + 11234 COSM110743 c.1529_1530insC p.D511fs*23 Insertion - Frameshift 6:137878974-137878975 + 4689 COSM35957 c.866_867delAC p.H289fs*6 Deletion - Frameshift 6:137877136-137877137 + PCSI_0058_Pa_X COSM3381431 c.487-6C>A p.? Unknown 6:137875682-137875682 + 2131 COSM35936 c.1817_1818insGTAAA p.C607fs*1 Insertion - Frameshift 6:137879262-137879263 + Pat_59_B COSM5869405 c.2260C>T p.P754S Substitution - Missense 6:137881206-137881206 + 1774985 COSM36249 c.305A>G p.N102S Substitution - Missense 6:137874854-137874854 + T2940 COSM3015726 c.1986C>T p.C662C Substitution - coding silent 6:137880150-137880150 + tumor_4131095 COSM5948685 c.917A>C p.Y306S Substitution - Missense 6:137877187-137877187 + 2108 COSM35940 c.484_485insG p.N163fs*4 Insertion - Frameshift 6:137875033-137875034 + 1737792 COSM303689 c.241_241delA p.K81fs*15 Deletion - Frameshift 6:137871468-137871468 + TCGA-HU-A4H3-01 COSM1440735 c.1167G>A p.T389T Substitution - coding silent 6:137878612-137878612 + PT53 COSM5941277 c.1115C>T p.P372L Substitution - Missense 6:137878560-137878560 + RC-K8 COSM36096 c.295+1G>A p.? Unknown 6:137871523-137871523 + SU-DHL-2 COSM35932 c.1376C>A p.S459* Substitution - Nonsense 6:137878821-137878821 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.211600 6q23 191163

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C IntronicSNV . c.1-1516A>C 6 138190849 CLL A C Missense p.K20Q c.58A>C 6 138192422 OV A C Missense p.K213Q c.637A>C 6 138197135 ESCA A G Missense p.D212G c.635A>G 6 138197133 PRAD A G Missense p.N776S c.2327A>G 6 138202410 OV A G Missense p.Y614C c.1841A>G 6 138200423 HNSC A G Missense p.Y778C c.2333A>G 6 138202416 LUSC C G Missense p.A588G c.1763C>G 6 138200345 COREAD C G Missense p.L421V c.1261C>G 6 138199843 OV C G Missense p.L591V c.1771C>G 6 138200353 LUAD C G Synonymous p.L147L c.441C>G 6 138196127 LUSC C T 3-UTRSNV . c.2370+116C>T 6 138202569 ESCA C T Missense p.A648V c.1943C>T 6 138201244 STAD C T Missense p.A764V c.2291C>T 6 138202374 STAD C T Missense p.T155M c.464C>T 6 138196150 STAD C T Synonymous p.F224F c.672C>T 6 138197170 BRCA C T Synonymous p.I63I c.189C>T 6 138192553 CM C T Synonymous p.L130L c.390C>T 6 138196076 CM C T Synonymous p.L324L c.972C>T 6 138198379 LUSC C T Synonymous p.N500N c.1500C>T 6 138200082 BRCA C T Synonymous p.S222S c.666C>T 6 138197164 CM C T Synonymous p.V644V c.1932C>T 6 138201233 RCCC GA - Frameshift p.E366Gfs*22 c.1097_1098delAG 6 138199674 UCEC G A Missense p.D285N c.853G>A 6 138198260 BLCA G A Missense p.E751K c.2251G>A 6 138202334 HNSC G A Missense p.E781K c.2341G>A 6 138202424 CM G A Missense p.G611S c.1831G>A 6 138200413 LUSC G A Missense p.R136H c.407G>A 6 138196093 LUSC G A Missense p.R411Q c.1232G>A 6 138199814 LGG G A Synonymous p.P576P c.1728G>A 6 138200310 BRCA G A Synonymous p.R280R c.840G>A 6 138198247 BLCA G C Missense p.L12F c.36G>C 6 138192400 BLCA G C Missense p.S217T c.650G>C 6 138197148 BRCA G C Synonymous p.A94A c.282G>C 6 138192646 LUSC - G IntronicInsertion . c.987-63dupG 6 138199506 ESCA G T Missense p.A327S c.979G>T 6 138198386 BRCA G T Missense p.D566Y c.1696G>T 6 138200278 COREAD G T Missense p.G622C c.1864G>T 6 138200446 LUSC G T Missense p.G777C c.2329G>T 6 138202412 ALL G T Missense p.S254I c.761G>T 6 138197259 STAD G T Synonymous p.A447A c.1341G>T 6 138199923 LUAD G T Synonymous p.G659G c.1977G>T 6 138201278 BRCA T A 3-UTRSNV . c.2370+828T>A 6 138203281 DLBCL T C Synonymous p.F197F c.591T>C 6 138196929 CM T G Missense p.C103G c.307T>G 6 138195993 OV