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 16 81348725 81348725 + Missense_Mutation SNP G G A TCGA-K4-A5RJ-01A-11D-A289-08 TCGA-K4-A5RJ-10A-01D-A289-08 g.chr16:81348725G>A c.7G>A c.(7-9)Gag>Aag p.E3K BLCA 16 81390451 81390451 + Missense_Mutation SNP G G A TCGA-S5-AA26-01A-11D-A38G-08 TCGA-S5-AA26-10A-01D-A38J-08 g.chr16:81390451G>A c.695G>A c.(694-696)cGg>cAg p.R232Q BLCA 16 81391457 81391457 + Silent SNP C C G TCGA-XF-A9T5-01A-11D-A42E-08 TCGA-XF-A9T5-10A-01D-A42H-08 g.chr16:81391457C>G c.894C>G c.(892-894)ctC>ctG p.L298L BLCA 16 81397453 81397453 + Missense_Mutation SNP G G A TCGA-GC-A3RB-01A-12D-A21Z-08 TCGA-GC-A3RB-10A-01D-A21Z-08 g.chr16:81397453G>A c.1141G>A c.(1141-1143)Gga>Aga p.G381R BLCA 16 81397481 81397481 + Missense_Mutation SNP C C G TCGA-SY-A9G5-01A-11D-A38G-08 TCGA-SY-A9G5-10A-01D-A38J-08 g.chr16:81397481C>G c.1169C>G c.(1168-1170)tCc>tGc p.S390C BLCA 16 81399016 81399016 + Missense_Mutation SNP C C T TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr16:81399016C>T c.1435C>T c.(1435-1437)Cgt>Tgt p.R479C BLCA 16 81411163 81411163 + Nonsense_Mutation SNP C C T TCGA-K4-A54R-01A-11D-A26M-08 TCGA-K4-A54R-10A-01D-A26K-08 g.chr16:81411163C>T c.1756C>T c.(1756-1758)Cag>Tag p.Q586* BRCA 16 81391441 81391441 + Missense_Mutation SNP G G A TCGA-E9-A54X-01A-11D-A25Q-09 TCGA-E9-A54X-10A-01D-A25Q-09 g.chr16:81391441G>A c.878G>A c.(877-879)cGa>cAa p.R293Q BRCA 16 81391485 81391485 + Missense_Mutation SNP G G A TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr16:81391485G>A c.922G>A c.(922-924)Gaa>Aaa p.E308K BRCA 16 81397481 81397481 + Missense_Mutation SNP C C A TCGA-A2-A0T6-01A-11D-A099-09 TCGA-A2-A0T6-10A-01D-A099-09 g.chr16:81397481C>A c.1169C>A c.(1168-1170)tCc>tAc p.S390Y CESC 16 81348827 81348827 + Missense_Mutation SNP G G C TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr16:81348827G>C c.109G>C c.(109-111)Gac>Cac p.D37H CESC 16 81411053 81411053 + Missense_Mutation SNP G G T TCGA-JW-A69B-01A-11D-A32I-09 TCGA-JW-A69B-10A-01D-A32I-09 g.chr16:81411053G>T c.1646G>T c.(1645-1647)aGa>aTa p.R549I COAD 16 81348861 81348861 + Missense_Mutation SNP T T C TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr16:81348861T>C c.143T>C c.(142-144)cTg>cCg p.L48P COAD 16 81385238 81385238 + Missense_Mutation SNP T T C TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr16:81385238T>C c.218T>C c.(217-219)aTt>aCt p.I73T COAD 16 81388061 81388061 + Silent SNP C C T TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr16:81388061C>T c.334C>T c.(334-336)Ctg>Ttg p.L112L COAD 16 81388170 81388170 + Missense_Mutation SNP A A G TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr16:81388170A>G c.443A>G c.(442-444)cAc>cGc p.H148R COAD 16 81388171 81388171 + Silent SNP C C T TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr16:81388171C>T c.444C>T c.(442-444)caC>caT p.H148H COAD 16 81388275 81388275 + Missense_Mutation SNP C C A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr16:81388275C>A c.548C>A c.(547-549)tCt>tAt p.S183Y COAD 16 81390538 81390538 + Missense_Mutation SNP C C T TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr16:81390538C>T c.782C>T c.(781-783)gCg>gTg p.A261V COAD 16 81391419 81391419 + Missense_Mutation SNP C C T TCGA-G4-6307-01A-11D-1719-10 TCGA-G4-6307-10A-01D-1720-10 g.chr16:81391419C>T c.856C>T c.(856-858)Cgg>Tgg p.R286W COAD 16 81391440 81391440 + Nonsense_Mutation SNP C C T TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr16:81391440C>T c.877C>T c.(877-879)Cga>Tga p.R293* COAD 16 81391440 81391440 + Nonsense_Mutation SNP C C T TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr16:81391440C>T c.877C>T c.(877-879)Cga>Tga p.R293* COAD 16 81397413 81397413 + Silent SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr16:81397413C>T c.1101C>T c.(1099-1101)ttC>ttT p.F367F COAD 16 81397494 81397494 + Silent SNP C C T TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr16:81397494C>T c.1182C>T c.(1180-1182)taC>taT p.Y394Y COAD 16 81410910 81410910 + Missense_Mutation SNP A A T TCGA-CM-6161-01A-11D-1650-10 TCGA-CM-6161-10A-01D-1650-10 g.chr16:81410910A>T c.1589A>T c.(1588-1590)tAt>tTt p.Y530F COAD 16 81411184 81411184 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr16:81411184C>T c.1777C>T c.(1777-1779)Cgt>Tgt p.R593C COADREAD 16 81348861 81348861 + Missense_Mutation SNP T T C TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr16:81348861T>C c.143T>C c.(142-144)cTg>cCg p.L48P COADREAD 16 81385237 81385237 + Missense_Mutation SNP A A G TCGA-F5-6813-01A-11D-1826-10 TCGA-F5-6813-10A-01D-1826-10 g.chr16:81385237A>G c.217A>G c.(217-219)Att>Gtt p.I73V COADREAD 16 81385238 81385238 + Missense_Mutation SNP T T C TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr16:81385238T>C c.218T>C c.(217-219)aTt>aCt p.I73T COADREAD 16 81388061 81388061 + Silent SNP C C T TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr16:81388061C>T c.334C>T c.(334-336)Ctg>Ttg p.L112L COADREAD 16 81388123 81388123 + Silent SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr16:81388123G>A c.396G>A c.(394-396)gaG>gaA p.E132E COADREAD 16 81388170 81388170 + Missense_Mutation SNP A A G TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr16:81388170A>G c.443A>G c.(442-444)cAc>cGc p.H148R COADREAD 16 81388171 81388171 + Silent SNP C C T TCGA-AA-3492-01A-01D-1408-10 TCGA-AA-3492-11A-01D-1408-10 g.chr16:81388171C>T c.444C>T c.(442-444)caC>caT p.H148H COADREAD 16 81388275 81388275 + Missense_Mutation SNP C C A TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr16:81388275C>A c.548C>A c.(547-549)tCt>tAt p.S183Y COADREAD 16 81388328 81388328 + Nonsense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr16:81388328C>T c.601C>T c.(601-603)Cga>Tga p.R201* COADREAD 16 81390538 81390538 + Missense_Mutation SNP C C T TCGA-A6-5665-01A-01D-1650-10 TCGA-A6-5665-10A-01D-1650-10 g.chr16:81390538C>T c.782C>T c.(781-783)gCg>gTg p.A261V COADREAD 16 81391419 81391419 + Missense_Mutation SNP C C T TCGA-G4-6307-01A-11D-1719-10 TCGA-G4-6307-10A-01D-1720-10 g.chr16:81391419C>T c.856C>T c.(856-858)Cgg>Tgg p.R286W COADREAD 16 81391440 81391440 + Nonsense_Mutation SNP C C T TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr16:81391440C>T c.877C>T c.(877-879)Cga>Tga p.R293* COADREAD 16 81391440 81391440 + Nonsense_Mutation SNP C C T TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr16:81391440C>T c.877C>T c.(877-879)Cga>Tga p.R293* COADREAD 16 81391484 81391484 + Silent SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr16:81391484C>T c.921C>T c.(919-921)atC>atT p.I307I COADREAD 16 81397413 81397413 + Silent SNP C C T TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr16:81397413C>T c.1101C>T c.(1099-1101)ttC>ttT p.F367F COADREAD 16 81397494 81397494 + Silent SNP C C T TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr16:81397494C>T c.1182C>T c.(1180-1182)taC>taT p.Y394Y COADREAD 16 81410910 81410910 + Missense_Mutation SNP A A T TCGA-CM-6161-01A-11D-1650-10 TCGA-CM-6161-10A-01D-1650-10 g.chr16:81410910A>T c.1589A>T c.(1588-1590)tAt>tTt p.Y530F COADREAD 16 81411184 81411184 + Missense_Mutation SNP C C T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr16:81411184C>T c.1777C>T c.(1777-1779)Cgt>Tgt p.R593C ESCA 16 81410849 81410849 + Silent SNP T T C TCGA-L5-A43J-01A-12D-A247-09 TCGA-L5-A43J-11A-11D-A247-09 g.chr16:81410849T>C c.1528T>C c.(1528-1530)Tta>Cta p.L510L GBM 16 81390535 81390535 + Missense_Mutation SNP A A G TCGA-12-1597-01B-01D-1495-08 TCGA-12-1597-10A-01D-1495-08 g.chr16:81390535A>G c.779A>G c.(778-780)gAg>gGg p.E260G GBMLGG 16 81388172 81388172 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:81388172G>A c.445G>A c.(445-447)Gtt>Att p.V149I GBMLGG 16 81390535 81390535 + Missense_Mutation SNP A A G TCGA-12-1597-01B-01D-1495-08 TCGA-12-1597-10A-01D-1495-08 g.chr16:81390535A>G c.779A>G c.(778-780)gAg>gGg p.E260G HNSC 16 81348778 81348778 + Silent SNP C C T TCGA-IQ-A61E-01A-22D-A30E-08 TCGA-IQ-A61E-10A-01D-A30H-08 g.chr16:81348778C>T c.60C>T c.(58-60)ctC>ctT p.L20L HNSC 16 81348783 81348783 + Missense_Mutation SNP C C G TCGA-IQ-A61E-01A-22D-A30E-08 TCGA-IQ-A61E-10A-01D-A30H-08 g.chr16:81348783C>G c.65C>G c.(64-66)tCt>tGt p.S22C HNSC 16 81388253 81388253 + Missense_Mutation SNP C C G TCGA-CV-6961-01A-21D-1912-08 TCGA-CV-6961-10A-01D-1912-08 g.chr16:81388253C>G c.526C>G c.(526-528)Caa>Gaa p.Q176E HNSC 16 81391435 81391435 + Missense_Mutation SNP C C T TCGA-IQ-A61E-01A-22D-A30E-08 TCGA-IQ-A61E-10A-01D-A30H-08 g.chr16:81391435C>T c.872C>T c.(871-873)gCg>gTg p.A291V HNSC 16 81396185 81396185 + Missense_Mutation SNP A A G TCGA-WA-A7H4-01A-21D-A34J-08 TCGA-WA-A7H4-10A-01D-A34M-08 g.chr16:81396185A>G c.1055A>G c.(1054-1056)aAt>aGt p.N352S HNSC 16 81399047 81399047 + Missense_Mutation SNP C C T TCGA-CV-6948-01A-11D-1912-08 TCGA-CV-6948-10A-01D-1912-08 g.chr16:81399047C>T c.1466C>T c.(1465-1467)aCt>aTt p.T489I KIPAN 16 81388211 81388211 + Silent SNP C C A TCGA-G7-6796-01A-11D-1961-08 TCGA-G7-6796-10A-01D-1962-08 g.chr16:81388211C>A c.484C>A c.(484-486)Cga>Aga p.R162R KIPAN 16 81391531 81391531 + Nonsense_Mutation SNP C C A TCGA-B2-3923-01A-01D-1458-08 TCGA-B2-3923-10A-01D-1458-08 g.chr16:81391531C>A c.968C>A c.(967-969)tCa>tAa p.S323* KIPAN 16 81398605 81398605 + Missense_Mutation SNP G G T TCGA-CZ-4865-01A-02D-1501-10 TCGA-CZ-4865-11A-01D-1501-10 g.chr16:81398605G>T c.1263G>T c.(1261-1263)aaG>aaT p.K421N KIPAN 16 81411067 81411067 + Missense_Mutation SNP T T G TCGA-BP-4347-01A-01D-1366-10 TCGA-BP-4347-11A-01D-1366-10 g.chr16:81411067T>G c.1660T>G c.(1660-1662)Tgg>Ggg p.W554G KIPAN 16 81411103 81411103 + Missense_Mutation SNP C C T TCGA-A4-7585-01A-11D-2136-08 TCGA-A4-7585-11A-01D-2136-08 g.chr16:81411103C>T c.1696C>T c.(1696-1698)Cgc>Tgc p.R566C KIRC 16 81391531 81391531 + Nonsense_Mutation SNP C C A TCGA-B2-3923-01A-01D-1458-08 TCGA-B2-3923-10A-01D-1458-08 g.chr16:81391531C>A c.968C>A c.(967-969)tCa>tAa p.S323* KIRC 16 81398605 81398605 + Missense_Mutation SNP G G T TCGA-CZ-4865-01A-02D-1501-10 TCGA-CZ-4865-11A-01D-1501-10 g.chr16:81398605G>T c.1263G>T c.(1261-1263)aaG>aaT p.K421N KIRC 16 81411067 81411067 + Missense_Mutation SNP T T G TCGA-BP-4347-01A-01D-1366-10 TCGA-BP-4347-11A-01D-1366-10 g.chr16:81411067T>G c.1660T>G c.(1660-1662)Tgg>Ggg p.W554G KIRP 16 81388211 81388211 + Silent SNP C C A TCGA-G7-6796-01A-11D-1961-08 TCGA-G7-6796-10A-01D-1962-08 g.chr16:81388211C>A c.484C>A c.(484-486)Cga>Aga p.R162R KIRP 16 81411103 81411103 + Missense_Mutation SNP C C T TCGA-A4-7585-01A-11D-2136-08 TCGA-A4-7585-11A-01D-2136-08 g.chr16:81411103C>T c.1696C>T c.(1696-1698)Cgc>Tgc p.R566C LGG 16 81388172 81388172 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr16:81388172G>A c.445G>A c.(445-447)Gtt>Att p.V149I LIHC 16 81385202 81385202 + Missense_Mutation SNP A A G TCGA-K7-AAU7-01A-11D-A382-10 TCGA-K7-AAU7-10A-01D-A385-10 g.chr16:81385202A>G c.182A>G c.(181-183)tAt>tGt p.Y61C LIHC 16 81390417 81390417 + Silent SNP C C T TCGA-K7-A6G5-01A-11D-A30V-10 TCGA-K7-A6G5-10A-01D-A30V-10 g.chr16:81390417C>T c.661C>T c.(661-663)Ctg>Ttg p.L221L LIHC 16 81411036 81411036 + Silent SNP C C T TCGA-4R-AA8I-01A-11D-A382-10 TCGA-4R-AA8I-10B-01D-A385-10 g.chr16:81411036C>T c.1629C>T c.(1627-1629)taC>taT p.Y543Y LUAD 16 81348805 81348805 + Missense_Mutation SNP C C G TCGA-78-7150-01A-21D-2036-08 TCGA-78-7150-10A-01D-2036-08 g.chr16:81348805C>G c.87C>G c.(85-87)ttC>ttG p.F29L LUAD 16 81385211 81385211 + Missense_Mutation SNP C C T TCGA-MP-A4TK-01A-11D-A24P-08 TCGA-MP-A4TK-10A-01D-A24P-08 g.chr16:81385211C>T c.191C>T c.(190-192)cCa>cTa p.P64L LUAD 16 81388139 81388139 + Missense_Mutation SNP C C G TCGA-05-4396-01A-21D-1855-08 TCGA-05-4396-10A-01D-1855-08 g.chr16:81388139C>G c.412C>G c.(412-414)Cgt>Ggt p.R138G LUAD 16 81388230 81388230 + Missense_Mutation SNP A A C TCGA-62-A46O-01A-11D-A24D-08 TCGA-62-A46O-10A-01D-A24F-08 g.chr16:81388230A>C c.503A>C c.(502-504)gAa>gCa p.E168A LUAD 16 81388292 81388292 + Missense_Mutation SNP G G T TCGA-05-4249-01A-01D-1105-08 TCGA-05-4249-10A-01D-1105-08 g.chr16:81388292G>T c.565G>T c.(565-567)Gtt>Ttt p.V189F LUAD 16 81388292 81388292 + Missense_Mutation SNP G G T TCGA-53-7626-01A-12D-2063-08 TCGA-53-7626-10A-01D-2063-08 g.chr16:81388292G>T c.565G>T c.(565-567)Gtt>Ttt p.V189F LUAD 16 81390414 81390414 + Missense_Mutation SNP G G T TCGA-91-6830-01A-11D-1945-08 TCGA-91-6830-11A-01D-1945-08 g.chr16:81390414G>T c.658G>T c.(658-660)Gct>Tct p.A220S LUAD 16 81391423 81391423 + Missense_Mutation SNP A A G TCGA-44-3918-01A-01D-1105-08 TCGA-44-3918-11A-01D-1105-08 g.chr16:81391423A>G c.860A>G c.(859-861)aAa>aGa p.K287R LUAD 16 81399073 81399073 + Missense_Mutation SNP G G A TCGA-55-7574-01A-11D-2036-08 TCGA-55-7574-10A-01D-2036-08 g.chr16:81399073G>A c.1492G>A c.(1492-1494)Gag>Aag p.E498K LUAD 16 81410934 81410934 + Splice_Site SNP G G C TCGA-49-4494-01A-01D-1265-08 TCGA-49-4494-11A-01D-1265-08 g.chr16:81410934G>C c.e10+1 LUSC 16 81397433 81397433 + Missense_Mutation SNP G G T TCGA-18-3414-01A-01D-0983-08 TCGA-18-3414-11A-01D-0983-08 g.chr16:81397433G>T c.1121G>T c.(1120-1122)gGg>gTg p.G374V OV 16 81385238 81385238 + Missense_Mutation SNP T T C TCGA-24-1464-01A-01W-0549-09 TCGA-24-1464-10A-01W-0549-09 g.chr16:81385238T>C c.218T>C c.(217-219)aTt>aCt p.I73T OV 16 81391420 81391420 + Missense_Mutation SNP G G A TCGA-23-1022-01A-02W-0488-09 TCGA-23-1022-10A-01W-0488-09 g.chr16:81391420G>A c.857G>A c.(856-858)cGg>cAg p.R286Q PAAD 16 81385228 81385228 + Missense_Mutation SNP A A G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr16:81385228A>G c.208A>G c.(208-210)Act>Gct p.T70A PAAD 16 81391435 81391435 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr16:81391435C>T c.872C>T c.(871-873)gCg>gTg p.A291V PAAD 16 81399055 81399055 + Missense_Mutation SNP T T C TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr16:81399055T>C c.1474T>C c.(1474-1476)Tcc>Ccc p.S492P PAAD 16 81411107 81411107 + Missense_Mutation SNP G G A TCGA-2J-AABR-01A-11D-A40W-08 TCGA-2J-AABR-10A-01D-A40W-08 g.chr16:81411107G>A c.1700G>A c.(1699-1701)cGt>cAt p.R567H PRAD 16 81390408 81390408 + Missense_Mutation SNP A A T TCGA-G9-7510-01A-11D-2260-08 TCGA-G9-7510-10A-01D-2260-08 g.chr16:81390408A>T c.652A>T c.(652-654)Atg>Ttg p.M218L READ 16 81385237 81385237 + Missense_Mutation SNP A A G TCGA-F5-6813-01A-11D-1826-10 TCGA-F5-6813-10A-01D-1826-10 g.chr16:81385237A>G c.217A>G c.(217-219)Att>Gtt p.I73V READ 16 81388123 81388123 + Silent SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr16:81388123G>A c.396G>A c.(394-396)gaG>gaA p.E132E READ 16 81388328 81388328 + Nonsense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr16:81388328C>T c.601C>T c.(601-603)Cga>Tga p.R201* READ 16 81391484 81391484 + Silent SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr16:81391484C>T c.921C>T c.(919-921)atC>atT p.I307I SARC 16 81391444 81391444 + Missense_Mutation SNP G G T TCGA-3B-A9I1-01A-11D-A38Z-09 TCGA-3B-A9I1-10A-01D-A38Z-09 g.chr16:81391444G>T c.881G>T c.(880-882)tGc>tTc p.C294F SKCM 16 81399011 81399011 + Missense_Mutation SNP G G A TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr16:81399011G>A c.1430G>A c.(1429-1431)cGa>cAa p.R477Q SKCM 16 81411074 81411074 + Missense_Mutation SNP A A C TCGA-D3-A2JA-06A-11D-A196-08 TCGA-D3-A2JA-10A-01D-A198-08 g.chr16:81411074A>C c.1667A>C c.(1666-1668)cAc>cCc p.H556P SKCM 16 81411177 81411177 + Silent SNP C C T TCGA-DA-A3F8-06A-11D-A20D-08 TCGA-DA-A3F8-10A-01D-A20D-08 g.chr16:81411177C>T c.1770C>T c.(1768-1770)ttC>ttT p.F590F

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BOCA-FR 16 81361590 81361590 single base substitution G A intron_variant BRCA-EU 16 81347082 81347082 single base substitution A C upstream_gene_variant BRCA-EU 16 81348575 81348575 single base substitution C T 5_prime_UTR_variant BRCA-EU 16 81348716 81348716 single base substitution G A 5_prime_UTR_variant BRCA-EU 16 81351253 81351253 single base substitution T C intron_variant BRCA-EU 16 81352463 81352463 single base substitution T C intron_variant BRCA-EU 16 81352502 81352502 single base substitution C T intron_variant BRCA-EU 16 81353492 81353492 single base substitution C G intron_variant BRCA-EU 16 81356409 81356409 single base substitution C T intron_variant BRCA-EU 16 81357602 81357602 deletion of <=200bp T - intron_variant BRCA-EU 16 81361154 81361154 single base substitution A G intron_variant BRCA-EU 16 81364013 81364013 single base substitution A T intron_variant BRCA-EU 16 81366483 81366483 single base substitution G T intron_variant BRCA-EU 16 81367680 81367680 single base substitution G C intron_variant BRCA-EU 16 81368511 81368511 single base substitution G T intron_variant BRCA-EU 16 81369469 81369469 single base substitution G C intron_variant BRCA-EU 16 81371797 81371797 deletion of <=200bp T - intron_variant BRCA-EU 16 81373607 81373607 single base substitution A G intron_variant BRCA-EU 16 81375606 81375606 single base substitution G A intron_variant BRCA-EU 16 81375642 81375642 single base substitution G T intron_variant BRCA-EU 16 81376692 81376692 single base substitution G A intron_variant BRCA-EU 16 81377159 81377159 single base substitution A G intron_variant BRCA-EU 16 81380657 81380657 single base substitution G A intron_variant BRCA-EU 16 81382261 81382261 single base substitution C T intron_variant BRCA-EU 16 81382352 81382352 single base substitution A G intron_variant BRCA-EU 16 81383082 81383082 single base substitution C G intron_variant BRCA-EU 16 81383612 81383612 single base substitution T A intron_variant BRCA-EU 16 81384469 81384469 single base substitution T A intron_variant BRCA-EU 16 81386877 81386877 single base substitution A C intron_variant BRCA-EU 16 81387430 81387430 single base substitution C T intron_variant BRCA-EU 16 81390109 81390109 single base substitution G C intron_variant BRCA-EU 16 81394555 81394555 single base substitution G A intron_variant BRCA-EU 16 81394555 81394555 single base substitution G A upstream_gene_variant BRCA-EU 16 81396068 81396068 single base substitution C G intron_variant BRCA-EU 16 81396068 81396068 single base substitution C G upstream_gene_variant BRCA-EU 16 81396837 81396837 single base substitution G A intron_variant BRCA-EU 16 81396837 81396837 single base substitution G A upstream_gene_variant BRCA-EU 16 81398904 81398904 single base substitution G T intron_variant BRCA-EU 16 81398904 81398904 single base substitution G T upstream_gene_variant BRCA-EU 16 81401937 81401937 single base substitution C A intron_variant BRCA-EU 16 81404501 81404501 single base substitution T C intron_variant BRCA-EU 16 81404506 81404506 single base substitution G A intron_variant BRCA-EU 16 81404761 81404761 single base substitution T C intron_variant BRCA-EU 16 81407899 81407899 single base substitution T A downstream_gene_variant BRCA-EU 16 81407899 81407899 single base substitution T A intron_variant BRCA-EU 16 81408106 81408106 single base substitution T C downstream_gene_variant BRCA-EU 16 81408106 81408106 single base substitution T C intron_variant BRCA-EU 16 81410522 81410522 single base substitution G C downstream_gene_variant BRCA-EU 16 81410522 81410522 single base substitution G C intron_variant BRCA-EU 16 81411403 81411403 single base substitution G T 3_prime_UTR_variant BRCA-EU 16 81411431 81411431 single base substitution G T 3_prime_UTR_variant BRCA-EU 16 81412894 81412894 single base substitution A G 3_prime_UTR_variant BRCA-EU 16 81416463 81416463 single base substitution C G 3_prime_UTR_variant BRCA-EU 16 81417527 81417527 single base substitution C T 3_prime_UTR_variant BRCA-EU 16 81418894 81418894 single base substitution A C 3_prime_UTR_variant BRCA-EU 16 81419092 81419092 single base substitution C T 3_prime_UTR_variant BRCA-EU 16 81420528 81420528 single base substitution C T 3_prime_UTR_variant BRCA-EU 16 81420745 81420745 single base substitution C T 3_prime_UTR_variant BRCA-EU 16 81421249 81421249 single base substitution C G 3_prime_UTR_variant BRCA-EU 16 81421439 81421439 single base substitution A T 3_prime_UTR_variant BRCA-EU 16 81422361 81422361 single base substitution G C 3_prime_UTR_variant BRCA-EU 16 81422860 81422860 single base substitution G A 3_prime_UTR_variant BRCA-EU 16 81423243 81423243 single base substitution A G 3_prime_UTR_variant BRCA-EU 16 81423911 81423911 single base substitution A C 3_prime_UTR_variant BRCA-EU 16 81424030 81424030 single base substitution G A 3_prime_UTR_variant BRCA-EU 16 81427612 81427612 single base substitution C T downstream_gene_variant BRCA-EU 16 81427639 81427639 single base substitution C A downstream_gene_variant BRCA-EU 16 81427921 81427923 deletion of <=200bp AAG - downstream_gene_variant BRCA-FR 16 81344253 81344253 single base substitution C T upstream_gene_variant BRCA-FR 16 81353492 81353492 single base substitution C G intron_variant BRCA-FR 16 81387430 81387430 single base substitution C T intron_variant BRCA-FR 16 81398110 81398110 single base substitution G A intron_variant BRCA-FR 16 81398110 81398110 single base substitution G A upstream_gene_variant BRCA-FR 16 81408890 81408890 single base substitution A C downstream_gene_variant BRCA-FR 16 81408890 81408890 single base substitution A C intron_variant BRCA-FR 16 81416463 81416463 single base substitution C G 3_prime_UTR_variant BRCA-FR 16 81417527 81417527 single base substitution C T 3_prime_UTR_variant BRCA-FR 16 81419092 81419092 single base substitution C T 3_prime_UTR_variant BRCA-UK 16 81352463 81352463 single base substitution T C intron_variant BRCA-UK 16 81361154 81361154 single base substitution A G intron_variant BRCA-US 16 81391441 81391441 single base substitution G A missense_variant R293Q 878G>A BRCA-US 16 81391485 81391485 single base substitution G A missense_variant E308K 922G>A BRCA-US 16 81397481 81397481 single base substitution C A missense_variant S390Y 1169C>A BRCA-US 16 81397481 81397481 single base substitution C A upstream_gene_variant BTCA-JP 16 81348981 81348981 single base substitution G C intron_variant BTCA-JP 16 81390500 81390500 single base substitution T C synonymous_variant C248C 744T>C BTCA-JP 16 81391507 81391507 single base substitution C T missense_variant P315L 944C>T BTCA-JP 16 81410927 81410927 single base substitution G A missense_variant D536N 1606G>A CESC-US 16 81348827 81348827 single base substitution G C missense_variant D37H 109G>C CESC-US 16 81411053 81411053 single base substitution G T missense_variant R549I 1646G>T CLLE-ES 16 81348152 81348152 single base substitution C T upstream_gene_variant CLLE-ES 16 81373860 81373860 single base substitution A G intron_variant CLLE-ES 16 81374950 81374950 single base substitution C G intron_variant CLLE-ES 16 81399111 81399111 single base substitution C G intron_variant CLLE-ES 16 81409400 81409400 single base substitution A T downstream_gene_variant CLLE-ES 16 81409400 81409400 single base substitution A T intron_variant CLLE-ES 16 81409461 81409461 single base substitution A G downstream_gene_variant CLLE-ES 16 81409461 81409461 single base substitution A G intron_variant CLLE-ES 16 81414428 81414428 single base substitution A G 3_prime_UTR_variant CLLE-ES 16 81415777 81415777 single base substitution A T 3_prime_UTR_variant COAD-US 16 81388061 81388061 single base substitution C T synonymous_variant L112L 334C>T COAD-US 16 81388171 81388171 single base substitution C T synonymous_variant H148H 444C>T COAD-US 16 81388275 81388275 single base substitution C A missense_variant S183Y 548C>A COAD-US 16 81390538 81390538 single base substitution C T missense_variant A261V 782C>T COAD-US 16 81397494 81397494 single base substitution C T synonymous_variant Y394Y 1182C>T COAD-US 16 81397494 81397494 single base substitution C T upstream_gene_variant COAD-US 16 81398635 81398635 single base substitution C T synonymous_variant Y431Y 1293C>T COAD-US 16 81398635 81398635 single base substitution C T upstream_gene_variant COAD-US 16 81398954 81398954 single base substitution G T splice_acceptor_variant COAD-US 16 81398954 81398954 single base substitution G T upstream_gene_variant COAD-US 16 81410910 81410910 single base substitution A T missense_variant Y530F 1589A>T COCA-CN 16 81388305 81388305 single base substitution G T missense_variant R193I 578G>T COCA-CN 16 81390481 81390481 single base substitution G A missense_variant R242Q 725G>A COCA-CN 16 81397238 81397238 single base substitution T C intron_variant COCA-CN 16 81397238 81397238 single base substitution T C upstream_gene_variant ESAD-UK 16 81343823 81343823 single base substitution C T upstream_gene_variant ESAD-UK 16 81344694 81344694 single base substitution T C upstream_gene_variant ESAD-UK 16 81344707 81344707 single base substitution C G upstream_gene_variant ESAD-UK 16 81345885 81345885 single base substitution T A upstream_gene_variant ESAD-UK 16 81346737 81346737 single base substitution G A upstream_gene_variant ESAD-UK 16 81347062 81347062 single base substitution C T upstream_gene_variant ESAD-UK 16 81347456 81347456 single base substitution T A upstream_gene_variant ESAD-UK 16 81348525 81348525 single base substitution T G upstream_gene_variant ESAD-UK 16 81348581 81348581 single base substitution C A 5_prime_UTR_variant ESAD-UK 16 81348938 81348939 deletion of <=200bp GC - intron_variant ESAD-UK 16 81350951 81350951 single base substitution A G intron_variant ESAD-UK 16 81356555 81356555 single base substitution G A intron_variant ESAD-UK 16 81358670 81358670 single base substitution C T intron_variant ESAD-UK 16 81360631 81360631 single base substitution G A intron_variant ESAD-UK 16 81361770 81361770 single base substitution A T intron_variant ESAD-UK 16 81362855 81362855 single base substitution G T intron_variant ESAD-UK 16 81368648 81368648 deletion of <=200bp T - intron_variant ESAD-UK 16 81369014 81369014 single base substitution C T intron_variant ESAD-UK 16 81373435 81373435 single base substitution G A intron_variant ESAD-UK 16 81373917 81373918 deletion of <=200bp AT - intron_variant ESAD-UK 16 81377758 81377758 single base substitution G A intron_variant ESAD-UK 16 81378210 81378210 single base substitution C A intron_variant ESAD-UK 16 81378920 81378920 single base substitution G A intron_variant ESAD-UK 16 81379964 81379964 single base substitution T G intron_variant ESAD-UK 16 81381174 81381174 single base substitution G A intron_variant ESAD-UK 16 81381929 81381929 single base substitution T A intron_variant ESAD-UK 16 81381930 81381930 single base substitution C G intron_variant ESAD-UK 16 81381931 81381931 single base substitution T A intron_variant ESAD-UK 16 81383566 81383566 single base substitution T A intron_variant ESAD-UK 16 81385170 81385170 deletion of <=200bp T - intron_variant ESAD-UK 16 81387150 81387150 single base substitution T A intron_variant ESAD-UK 16 81389286 81389286 single base substitution C T intron_variant ESAD-UK 16 81396814 81396814 single base substitution T G intron_variant ESAD-UK 16 81396814 81396814 single base substitution T G upstream_gene_variant ESAD-UK 16 81397930 81397930 single base substitution G A intron_variant ESAD-UK 16 81397930 81397930 single base substitution G A upstream_gene_variant ESAD-UK 16 81398198 81398198 single base substitution G A intron_variant ESAD-UK 16 81398198 81398198 single base substitution G A upstream_gene_variant ESAD-UK 16 81399013 81399013 single base substitution A C missense_variant S478R 1432A>C ESAD-UK 16 81399013 81399013 single base substitution A C upstream_gene_variant ESAD-UK 16 81400680 81400680 single base substitution A G intron_variant ESAD-UK 16 81409928 81409928 single base substitution G A downstream_gene_variant ESAD-UK 16 81409928 81409928 single base substitution G A intron_variant ESAD-UK 16 81410313 81410313 insertion of <=200bp - AC downstream_gene_variant ESAD-UK 16 81410313 81410313 insertion of <=200bp - AC intron_variant ESAD-UK 16 81410973 81410973 single base substitution G A intron_variant ESAD-UK 16 81414734 81414734 insertion of <=200bp - AGAGAGGACTG 3_prime_UTR_variant ESAD-UK 16 81414827 81414827 single base substitution G A 3_prime_UTR_variant ESAD-UK 16 81415945 81415945 single base substitution G A 3_prime_UTR_variant ESAD-UK 16 81417777 81417777 single base substitution A T 3_prime_UTR_variant ESAD-UK 16 81418630 81418630 single base substitution G A 3_prime_UTR_variant ESAD-UK 16 81422581 81422581 single base substitution A T 3_prime_UTR_variant ESCA-CN 16 81396214 81396214 single base substitution G A missense_variant E362K 1084G>A ESCA-CN 16 81396214 81396214 single base substitution G A upstream_gene_variant ESCA-CN 16 81410861 81410861 single base substitution G A missense_variant A514T 1540G>A ESCA-CN 16 81411448 81411448 single base substitution G A 3_prime_UTR_variant ESCA-CN 16 81411673 81411673 single base substitution C G 3_prime_UTR_variant GBM-US 16 81390535 81390535 single base substitution A G missense_variant E260G 779A>G KIRC-US 16 81398605 81398605 single base substitution G T missense_variant K421N 1263G>T KIRC-US 16 81398605 81398605 single base substitution G T upstream_gene_variant KIRC-US 16 81411067 81411067 single base substitution T G missense_variant W554G 1660T>G KIRP-US 16 81411103 81411103 single base substitution C T missense_variant R566C 1696C>T LAML-KR 16 81424648 81424648 single base substitution T C downstream_gene_variant LICA-FR 16 81365584 81365584 single base substitution A G intron_variant LICA-FR 16 81370459 81370459 single base substitution C T intron_variant LICA-FR 16 81394448 81394448 single base substitution C G intron_variant LICA-FR 16 81394448 81394448 single base substitution C G upstream_gene_variant LICA-FR 16 81401458 81401458 single base substitution A T intron_variant LICA-FR 16 81403844 81403844 single base substitution T C intron_variant LICA-FR 16 81424633 81424633 single base substitution C G downstream_gene_variant LIHC-US 16 81390417 81390417 single base substitution C T synonymous_variant L221L 661C>T LINC-JP 16 81348597 81348597 single base substitution G T 5_prime_UTR_variant LINC-JP 16 81373301 81373301 single base substitution C T intron_variant LINC-JP 16 81383822 81383822 single base substitution C T intron_variant LINC-JP 16 81387769 81387769 single base substitution C T intron_variant LINC-JP 16 81392550 81392550 single base substitution A T intron_variant LINC-JP 16 81396107 81396107 single base substitution G T missense_variant G326V 977G>T LINC-JP 16 81396107 81396107 single base substitution G T upstream_gene_variant LINC-JP 16 81420294 81420294 single base substitution G A 3_prime_UTR_variant LINC-JP 16 81424675 81424675 single base substitution T C downstream_gene_variant LINC-JP 16 81427958 81427958 single base substitution A G downstream_gene_variant LIRI-JP 16 81344107 81344107 single base substitution A G upstream_gene_variant LIRI-JP 16 81344408 81344408 single base substitution T C upstream_gene_variant LIRI-JP 16 81345554 81345554 single base substitution T C upstream_gene_variant LIRI-JP 16 81345836 81345836 single base substitution T G upstream_gene_variant LIRI-JP 16 81363847 81363847 single base substitution A G intron_variant LIRI-JP 16 81367677 81367677 single base substitution C T intron_variant LIRI-JP 16 81371929 81371929 single base substitution T C intron_variant LIRI-JP 16 81372548 81372548 single base substitution G C intron_variant LIRI-JP 16 81376926 81376926 single base substitution G T intron_variant LIRI-JP 16 81380693 81380693 single base substitution A G intron_variant LIRI-JP 16 81381098 81381098 single base substitution T G intron_variant LIRI-JP 16 81381672 81381672 single base substitution G A intron_variant LIRI-JP 16 81382294 81382294 single base substitution G C intron_variant LIRI-JP 16 81384668 81384668 single base substitution A G intron_variant LIRI-JP 16 81385254 81385254 single base substitution A G missense_variant I78M 234A>G LIRI-JP 16 81389651 81389651 deletion of <=200bp T - intron_variant LIRI-JP 16 81389904 81389905 deletion of <=200bp TA - intron_variant LIRI-JP 16 81390329 81390329 single base substitution C T intron_variant LIRI-JP 16 81393431 81393431 single base substitution C T intron_variant LIRI-JP 16 81396726 81396726 single base substitution G T intron_variant LIRI-JP 16 81396726 81396726 single base substitution G T upstream_gene_variant LIRI-JP 16 81398735 81398735 single base substitution A G intron_variant LIRI-JP 16 81398735 81398735 single base substitution A G upstream_gene_variant LIRI-JP 16 81401620 81401620 single base substitution A G intron_variant LIRI-JP 16 81403593 81403593 single base substitution A T intron_variant LIRI-JP 16 81405499 81405499 single base substitution G A exon_variant LIRI-JP 16 81405499 81405499 single base substitution G A intron_variant LIRI-JP 16 81409042 81409042 single base substitution A G downstream_gene_variant LIRI-JP 16 81409042 81409042 single base substitution A G intron_variant LIRI-JP 16 81412003 81412003 single base substitution G A 3_prime_UTR_variant LIRI-JP 16 81413683 81413683 single base substitution A G 3_prime_UTR_variant LIRI-JP 16 81416652 81416652 single base substitution C T 3_prime_UTR_variant LIRI-JP 16 81418995 81418995 single base substitution A G 3_prime_UTR_variant LIRI-JP 16 81420985 81420985 single base substitution G A 3_prime_UTR_variant LIRI-JP 16 81421459 81421459 single base substitution A G 3_prime_UTR_variant LIRI-JP 16 81421932 81421932 single base substitution A C 3_prime_UTR_variant LIRI-JP 16 81424347 81424347 single base substitution T C 3_prime_UTR_variant LIRI-JP 16 81425796 81425796 single base substitution A T downstream_gene_variant LUSC-KR 16 81345928 81345928 single base substitution G C upstream_gene_variant LUSC-KR 16 81349566 81349566 single base substitution G A intron_variant LUSC-KR 16 81350351 81350351 single base substitution G A intron_variant LUSC-KR 16 81350931 81350931 single base substitution G C intron_variant LUSC-KR 16 81351390 81351390 single base substitution G C intron_variant LUSC-KR 16 81351893 81351893 single base substitution A G intron_variant LUSC-KR 16 81351973 81351973 single base substitution G C intron_variant LUSC-KR 16 81352687 81352687 single base substitution G A intron_variant LUSC-KR 16 81358330 81358330 single base substitution G C intron_variant LUSC-KR 16 81358827 81358827 single base substitution A G intron_variant LUSC-KR 16 81359426 81359426 single base substitution G C intron_variant LUSC-KR 16 81369124 81369124 single base substitution G T intron_variant LUSC-KR 16 81371549 81371549 single base substitution G A intron_variant LUSC-KR 16 81372410 81372410 single base substitution G C intron_variant LUSC-KR 16 81374271 81374271 single base substitution A T intron_variant LUSC-KR 16 81374864 81374864 single base substitution G T intron_variant LUSC-KR 16 81376692 81376692 single base substitution G A intron_variant LUSC-KR 16 81379495 81379495 single base substitution C T intron_variant LUSC-KR 16 81382677 81382677 single base substitution G C intron_variant LUSC-KR 16 81383236 81383236 single base substitution G A intron_variant LUSC-KR 16 81389349 81389349 single base substitution G T intron_variant LUSC-KR 16 81391196 81391196 single base substitution G A intron_variant LUSC-KR 16 81400232 81400232 single base substitution C T intron_variant LUSC-KR 16 81401170 81401170 single base substitution A G intron_variant LUSC-KR 16 81408356 81408356 single base substitution G T downstream_gene_variant LUSC-KR 16 81408356 81408356 single base substitution G T intron_variant LUSC-KR 16 81416876 81416876 single base substitution G T 3_prime_UTR_variant LUSC-KR 16 81420836 81420836 single base substitution G T 3_prime_UTR_variant LUSC-KR 16 81424648 81424648 single base substitution T C downstream_gene_variant LUSC-KR 16 81428880 81428880 single base substitution A G downstream_gene_variant LUSC-US 16 81397433 81397433 single base substitution G T missense_variant G374V 1121G>T LUSC-US 16 81397433 81397433 single base substitution G T upstream_gene_variant MALY-DE 16 81363719 81363719 single base substitution G C intron_variant MALY-DE 16 81366907 81366907 single base substitution A G intron_variant MALY-DE 16 81377261 81377261 single base substitution A G intron_variant MALY-DE 16 81379986 81380004 deletion of <=200bp GGCCTTAGGACTGGGCCAT - intron_variant MALY-DE 16 81381148 81381148 single base substitution T G intron_variant MALY-DE 16 81382631 81382631 single base substitution A G intron_variant MALY-DE 16 81393658 81393658 single base substitution G A intron_variant MALY-DE 16 81403353 81403353 single base substitution C T intron_variant MALY-DE 16 81403599 81403599 single base substitution A G intron_variant MALY-DE 16 81406659 81406659 single base substitution T G downstream_gene_variant MALY-DE 16 81406659 81406659 single base substitution T G intron_variant MALY-DE 16 81413524 81413524 single base substitution T A 3_prime_UTR_variant MALY-DE 16 81418175 81418175 single base substitution T A 3_prime_UTR_variant MALY-DE 16 81421291 81421291 single base substitution G A 3_prime_UTR_variant MALY-DE 16 81427528 81427528 single base substitution A C downstream_gene_variant MALY-DE 16 81428061 81428061 single base substitution A C downstream_gene_variant MALY-DE 16 81428748 81428748 single base substitution G A downstream_gene_variant MELA-AU 16 81343564 81343564 single base substitution G A upstream_gene_variant MELA-AU 16 81343571 81343571 single base substitution G A upstream_gene_variant MELA-AU 16 81343952 81343952 single base substitution C T upstream_gene_variant MELA-AU 16 81344066 81344066 single base substitution T A upstream_gene_variant MELA-AU 16 81344300 81344300 single base substitution A T upstream_gene_variant MELA-AU 16 81344603 81344603 single base substitution C T upstream_gene_variant MELA-AU 16 81345046 81345046 single base substitution G A upstream_gene_variant MELA-AU 16 81345561 81345561 single base substitution G A upstream_gene_variant MELA-AU 16 81345812 81345812 single base substitution C T upstream_gene_variant MELA-AU 16 81346292 81346292 single base substitution G A upstream_gene_variant MELA-AU 16 81346587 81346587 single base substitution G A upstream_gene_variant MELA-AU 16 81346663 81346663 single base substitution G A upstream_gene_variant MELA-AU 16 81346723 81346723 single base substitution A T upstream_gene_variant MELA-AU 16 81346866 81346866 single base substitution G A upstream_gene_variant MELA-AU 16 81347528 81347528 single base substitution A G upstream_gene_variant MELA-AU 16 81348367 81348367 single base substitution C T upstream_gene_variant MELA-AU 16 81348490 81348490 single base substitution G A upstream_gene_variant MELA-AU 16 81349101 81349101 single base substitution C T intron_variant MELA-AU 16 81350848 81350848 single base substitution C T intron_variant MELA-AU 16 81351293 81351293 single base substitution C T intron_variant MELA-AU 16 81351841 81351841 single base substitution C T intron_variant MELA-AU 16 81351954 81351954 single base substitution T A intron_variant MELA-AU 16 81352015 81352015 single base substitution C T intron_variant MELA-AU 16 81352047 81352047 single base substitution C T intron_variant MELA-AU 16 81353121 81353121 single base substitution C T intron_variant MELA-AU 16 81354594 81354594 single base substitution G A intron_variant MELA-AU 16 81355124 81355124 single base substitution T C intron_variant MELA-AU 16 81356680 81356680 single base substitution C T intron_variant MELA-AU 16 81357410 81357410 single base substitution C T intron_variant MELA-AU 16 81357583 81357583 single base substitution T A intron_variant MELA-AU 16 81357765 81357765 single base substitution C T intron_variant MELA-AU 16 81358304 81358304 single base substitution A G intron_variant MELA-AU 16 81358419 81358419 single base substitution T G intron_variant MELA-AU 16 81358704 81358704 single base substitution C T intron_variant MELA-AU 16 81359378 81359378 single base substitution C T intron_variant MELA-AU 16 81359440 81359440 single base substitution G T intron_variant MELA-AU 16 81360787 81360787 single base substitution G A intron_variant MELA-AU 16 81361100 81361100 single base substitution C T intron_variant MELA-AU 16 81361335 81361335 single base substitution C T intron_variant MELA-AU 16 81361394 81361394 single base substitution G T intron_variant MELA-AU 16 81362305 81362305 single base substitution C T intron_variant MELA-AU 16 81362544 81362544 single base substitution C T intron_variant MELA-AU 16 81362590 81362590 single base substitution C T intron_variant MELA-AU 16 81363153 81363153 single base substitution C T intron_variant MELA-AU 16 81363463 81363463 single base substitution C T intron_variant MELA-AU 16 81363471 81363471 single base substitution C T intron_variant MELA-AU 16 81364341 81364341 single base substitution G A intron_variant MELA-AU 16 81365097 81365097 single base substitution A T intron_variant MELA-AU 16 81365179 81365179 single base substitution C T intron_variant MELA-AU 16 81365181 81365181 single base substitution C T intron_variant MELA-AU 16 81365251 81365251 single base substitution C T intron_variant MELA-AU 16 81365356 81365356 single base substitution C T intron_variant MELA-AU 16 81365516 81365516 single base substitution C T intron_variant MELA-AU 16 81365645 81365645 single base substitution G T intron_variant MELA-AU 16 81366107 81366107 single base substitution C T intron_variant MELA-AU 16 81366285 81366285 single base substitution C T intron_variant MELA-AU 16 81367129 81367129 single base substitution A G intron_variant MELA-AU 16 81367414 81367414 single base substitution G A intron_variant MELA-AU 16 81367503 81367503 single base substitution C T intron_variant MELA-AU 16 81367663 81367663 single base substitution C T intron_variant MELA-AU 16 81367667 81367667 single base substitution C T intron_variant MELA-AU 16 81367670 81367670 single base substitution C T intron_variant MELA-AU 16 81368308 81368308 single base substitution C T intron_variant MELA-AU 16 81369517 81369517 single base substitution C T intron_variant MELA-AU 16 81369662 81369662 single base substitution C T intron_variant MELA-AU 16 81369867 81369867 single base substitution G A intron_variant MELA-AU 16 81370225 81370225 single base substitution C T intron_variant MELA-AU 16 81370253 81370253 single base substitution T A intron_variant MELA-AU 16 81370373 81370373 single base substitution A T intron_variant MELA-AU 16 81371254 81371254 single base substitution G A intron_variant MELA-AU 16 81371256 81371256 single base substitution C A intron_variant MELA-AU 16 81371330 81371330 single base substitution C T intron_variant MELA-AU 16 81371697 81371697 single base substitution T G intron_variant MELA-AU 16 81371799 81371799 insertion of <=200bp - A intron_variant MELA-AU 16 81371804 81371804 single base substitution T G intron_variant MELA-AU 16 81372923 81372923 single base substitution C T intron_variant MELA-AU 16 81373086 81373086 single base substitution A T intron_variant MELA-AU 16 81373567 81373567 single base substitution C T intron_variant MELA-AU 16 81374669 81374669 single base substitution G A intron_variant MELA-AU 16 81374860 81374860 single base substitution G A intron_variant MELA-AU 16 81375371 81375371 single base substitution C T intron_variant MELA-AU 16 81376201 81376201 single base substitution A T intron_variant MELA-AU 16 81376417 81376417 single base substitution C T intron_variant MELA-AU 16 81376720 81376720 single base substitution C T intron_variant MELA-AU 16 81376754 81376754 single base substitution C T intron_variant MELA-AU 16 81376943 81376943 single base substitution C T intron_variant MELA-AU 16 81377595 81377595 single base substitution C T intron_variant MELA-AU 16 81377602 81377602 single base substitution G A intron_variant MELA-AU 16 81377875 81377875 single base substitution C T intron_variant MELA-AU 16 81378187 81378187 single base substitution C T intron_variant MELA-AU 16 81378261 81378261 single base substitution C T intron_variant MELA-AU 16 81378313 81378313 single base substitution C T intron_variant MELA-AU 16 81378523 81378523 single base substitution C A intron_variant MELA-AU 16 81379469 81379469 single base substitution C T intron_variant MELA-AU 16 81379574 81379574 single base substitution A C intron_variant MELA-AU 16 81379957 81379957 single base substitution G C intron_variant MELA-AU 16 81380007 81380007 single base substitution C T intron_variant MELA-AU 16 81380268 81380268 single base substitution C T intron_variant MELA-AU 16 81380759 81380759 single base substitution C G intron_variant MELA-AU 16 81381172 81381172 single base substitution C T intron_variant MELA-AU 16 81381236 81381236 single base substitution C T intron_variant MELA-AU 16 81381374 81381374 single base substitution C T intron_variant MELA-AU 16 81381553 81381553 single base substitution T C intron_variant MELA-AU 16 81381654 81381654 single base substitution C T intron_variant MELA-AU 16 81381961 81381961 single base substitution C T intron_variant MELA-AU 16 81382678 81382678 single base substitution A C intron_variant MELA-AU 16 81382838 81382839 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 16 81382864 81382864 single base substitution C T intron_variant MELA-AU 16 81382881 81382881 single base substitution C T intron_variant MELA-AU 16 81383654 81383654 single base substitution C T intron_variant MELA-AU 16 81383711 81383711 single base substitution C T intron_variant MELA-AU 16 81385376 81385376 single base substitution C T intron_variant MELA-AU 16 81386170 81386170 single base substitution C T intron_variant MELA-AU 16 81386293 81386293 single base substitution T G intron_variant MELA-AU 16 81386476 81386476 single base substitution C T intron_variant MELA-AU 16 81386535 81386535 single base substitution C T intron_variant MELA-AU 16 81387216 81387216 single base substitution C T intron_variant MELA-AU 16 81387928 81387928 single base substitution C T intron_variant MELA-AU 16 81389001 81389001 single base substitution C T intron_variant MELA-AU 16 81389002 81389002 single base substitution C T intron_variant MELA-AU 16 81389052 81389052 single base substitution C T intron_variant MELA-AU 16 81389460 81389461 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 16 81390116 81390116 single base substitution C T intron_variant MELA-AU 16 81391457 81391457 single base substitution C T synonymous_variant L298L 894C>T MELA-AU 16 81391494 81391494 single base substitution C T missense_variant P311S 931C>T MELA-AU 16 81393538 81393538 single base substitution C T intron_variant MELA-AU 16 81393670 81393670 single base substitution G A intron_variant MELA-AU 16 81393706 81393706 single base substitution G A intron_variant MELA-AU 16 81395070 81395070 single base substitution C T intron_variant MELA-AU 16 81395070 81395070 single base substitution C T upstream_gene_variant MELA-AU 16 81395335 81395335 single base substitution C T intron_variant MELA-AU 16 81395335 81395335 single base substitution C T upstream_gene_variant MELA-AU 16 81395666 81395666 single base substitution C T intron_variant MELA-AU 16 81395666 81395666 single base substitution C T upstream_gene_variant MELA-AU 16 81396663 81396663 single base substitution C T intron_variant MELA-AU 16 81396663 81396663 single base substitution C T upstream_gene_variant MELA-AU 16 81397882 81397882 single base substitution C T intron_variant MELA-AU 16 81397882 81397882 single base substitution C T upstream_gene_variant MELA-AU 16 81398836 81398836 single base substitution C T intron_variant MELA-AU 16 81398836 81398836 single base substitution C T upstream_gene_variant MELA-AU 16 81399655 81399655 single base substitution C T intron_variant MELA-AU 16 81400444 81400444 single base substitution T G intron_variant MELA-AU 16 81400638 81400638 single base substitution C T intron_variant MELA-AU 16 81401442 81401442 single base substitution T A intron_variant MELA-AU 16 81401682 81401682 single base substitution C T intron_variant MELA-AU 16 81402312 81402312 single base substitution C T intron_variant MELA-AU 16 81402622 81402622 single base substitution C T intron_variant MELA-AU 16 81402764 81402764 single base substitution C T intron_variant MELA-AU 16 81402833 81402833 single base substitution C T intron_variant MELA-AU 16 81404165 81404165 single base substitution C T intron_variant MELA-AU 16 81404384 81404384 single base substitution C T intron_variant MELA-AU 16 81404551 81404551 single base substitution C T intron_variant MELA-AU 16 81404815 81404815 single base substitution C T intron_variant MELA-AU 16 81405246 81405246 single base substitution C T intron_variant MELA-AU 16 81405356 81405356 single base substitution T C intron_variant MELA-AU 16 81405425 81405425 single base substitution C T intron_variant MELA-AU 16 81406153 81406153 single base substitution C T downstream_gene_variant MELA-AU 16 81406153 81406153 single base substitution C T intron_variant MELA-AU 16 81406633 81406633 insertion of <=200bp - A downstream_gene_variant MELA-AU 16 81406633 81406633 insertion of <=200bp - A intron_variant MELA-AU 16 81406660 81406660 single base substitution C T downstream_gene_variant MELA-AU 16 81406660 81406660 single base substitution C T intron_variant MELA-AU 16 81407167 81407167 single base substitution C T downstream_gene_variant MELA-AU 16 81407167 81407167 single base substitution C T intron_variant MELA-AU 16 81407377 81407377 single base substitution C T downstream_gene_variant MELA-AU 16 81407377 81407377 single base substitution C T intron_variant MELA-AU 16 81407603 81407603 single base substitution C T downstream_gene_variant MELA-AU 16 81407603 81407603 single base substitution C T intron_variant MELA-AU 16 81407695 81407695 single base substitution T G downstream_gene_variant MELA-AU 16 81407695 81407695 single base substitution T G intron_variant MELA-AU 16 81407747 81407747 single base substitution T G downstream_gene_variant MELA-AU 16 81407747 81407747 single base substitution T G intron_variant MELA-AU 16 81407965 81407965 single base substitution G A downstream_gene_variant MELA-AU 16 81407965 81407965 single base substitution G A intron_variant MELA-AU 16 81407967 81407967 single base substitution G A downstream_gene_variant MELA-AU 16 81407967 81407967 single base substitution G A intron_variant MELA-AU 16 81407984 81407984 single base substitution T A downstream_gene_variant MELA-AU 16 81407984 81407984 single base substitution T A intron_variant MELA-AU 16 81408135 81408135 single base substitution C T downstream_gene_variant MELA-AU 16 81408135 81408135 single base substitution C T intron_variant MELA-AU 16 81408243 81408243 single base substitution C G downstream_gene_variant MELA-AU 16 81408243 81408243 single base substitution C G intron_variant MELA-AU 16 81409424 81409424 single base substitution C T downstream_gene_variant MELA-AU 16 81409424 81409424 single base substitution C T intron_variant MELA-AU 16 81409882 81409883 multiple base substitution (>=2bp and <=200bp) CA AT downstream_gene_variant MELA-AU 16 81409882 81409883 multiple base substitution (>=2bp and <=200bp) CA AT intron_variant MELA-AU 16 81411400 81411400 single base substitution G A 3_prime_UTR_variant MELA-AU 16 81412158 81412158 single base substitution C T 3_prime_UTR_variant MELA-AU 16 81412407 81412407 single base substitution C T 3_prime_UTR_variant MELA-AU 16 81412568 81412568 single base substitution A G 3_prime_UTR_variant MELA-AU 16 81412652 81412652 single base substitution T C 3_prime_UTR_variant MELA-AU 16 81412657 81412657 single base substitution C T 3_prime_UTR_variant MELA-AU 16 81412826 81412826 single base substitution A G 3_prime_UTR_variant MELA-AU 16 81413343 81413343 single base substitution C T 3_prime_UTR_variant MELA-AU 16 81413523 81413523 single base substitution T G 3_prime_UTR_variant MELA-AU 16 81416888 81416888 single base substitution C T 3_prime_UTR_variant MELA-AU 16 81417254 81417254 single base substitution C T 3_prime_UTR_variant MELA-AU 16 81417511 81417511 single base substitution A G 3_prime_UTR_variant MELA-AU 16 81417750 81417750 single base substitution C T 3_prime_UTR_variant MELA-AU 16 81417893 81417893 single base substitution C T 3_prime_UTR_variant MELA-AU 16 81418382 81418382 single base substitution C A 3_prime_UTR_variant MELA-AU 16 81418705 81418705 single base substitution C T 3_prime_UTR_variant MELA-AU 16 81419854 81419854 single base substitution C T 3_prime_UTR_variant MELA-AU 16 81419916 81419916 single base substitution C T 3_prime_UTR_variant MELA-AU 16 81420467 81420467 single base substitution C T 3_prime_UTR_variant MELA-AU 16 81420821 81420821 single base substitution G A 3_prime_UTR_variant MELA-AU 16 81421200 81421200 single base substitution C T 3_prime_UTR_variant MELA-AU 16 81421303 81421303 single base substitution C T 3_prime_UTR_variant MELA-AU 16 81421923 81421923 single base substitution C T 3_prime_UTR_variant MELA-AU 16 81421993 81421993 single base substitution C T 3_prime_UTR_variant MELA-AU 16 81422129 81422129 single base substitution C A 3_prime_UTR_variant MELA-AU 16 81422151 81422151 single base substitution C T 3_prime_UTR_variant MELA-AU 16 81422250 81422251 multiple base substitution (>=2bp and <=200bp) CC TT 3_prime_UTR_variant MELA-AU 16 81422679 81422679 single base substitution C T 3_prime_UTR_variant MELA-AU 16 81422852 81422852 single base substitution T C 3_prime_UTR_variant MELA-AU 16 81423132 81423132 single base substitution C T 3_prime_UTR_variant MELA-AU 16 81423308 81423308 single base substitution C A 3_prime_UTR_variant MELA-AU 16 81423778 81423778 single base substitution C T 3_prime_UTR_variant MELA-AU 16 81423998 81423998 single base substitution T C 3_prime_UTR_variant MELA-AU 16 81424630 81424630 single base substitution C T downstream_gene_variant MELA-AU 16 81425144 81425144 single base substitution C T downstream_gene_variant MELA-AU 16 81425341 81425341 single base substitution C T downstream_gene_variant MELA-AU 16 81425658 81425658 single base substitution G A downstream_gene_variant MELA-AU 16 81425750 81425750 single base substitution A G downstream_gene_variant MELA-AU 16 81426195 81426195 single base substitution C T downstream_gene_variant MELA-AU 16 81426889 81426889 single base substitution T C downstream_gene_variant MELA-AU 16 81427421 81427421 single base substitution A T downstream_gene_variant MELA-AU 16 81427868 81427868 single base substitution C T downstream_gene_variant MELA-AU 16 81427990 81427990 single base substitution G A downstream_gene_variant MELA-AU 16 81428210 81428210 single base substitution C T downstream_gene_variant MELA-AU 16 81428276 81428276 single base substitution G A downstream_gene_variant MELA-AU 16 81428783 81428783 single base substitution C T downstream_gene_variant MELA-AU 16 81429379 81429379 single base substitution C T downstream_gene_variant ORCA-IN 16 81360752 81360752 single base substitution G T intron_variant ORCA-IN 16 81388061 81388061 single base substitution C T synonymous_variant L112L 334C>T ORCA-IN 16 81389353 81389353 single base substitution G A intron_variant ORCA-IN 16 81403304 81403304 single base substitution C G intron_variant ORCA-IN 16 81424681 81424681 single base substitution G C downstream_gene_variant ORCA-IN 16 81427844 81427844 single base substitution G A downstream_gene_variant ORCA-IN 16 81428746 81428746 single base substitution C G downstream_gene_variant OV-AU 16 81354666 81354666 single base substitution G C intron_variant OV-AU 16 81364466 81364466 single base substitution A G intron_variant OV-AU 16 81370335 81370335 single base substitution G A intron_variant OV-AU 16 81373233 81373233 single base substitution T A intron_variant OV-AU 16 81376033 81376033 single base substitution A T intron_variant OV-AU 16 81385020 81385020 single base substitution A G intron_variant OV-AU 16 81388253 81388253 single base substitution C A missense_variant Q176K 526C>A OV-AU 16 81393616 81393616 single base substitution T A intron_variant OV-AU 16 81401285 81401285 single base substitution A G intron_variant OV-AU 16 81407177 81407177 single base substitution G A downstream_gene_variant OV-AU 16 81407177 81407177 single base substitution G A intron_variant OV-AU 16 81417100 81417100 single base substitution C T 3_prime_UTR_variant OV-AU 16 81421889 81421889 single base substitution G T 3_prime_UTR_variant OV-AU 16 81425025 81425025 single base substitution C T downstream_gene_variant OV-US 16 81385238 81385238 single base substitution T C missense_variant I73T 218T>C OV-US 16 81391420 81391420 single base substitution G A missense_variant R286Q 857G>A PACA-AU 16 81350567 81350567 single base substitution G A intron_variant PACA-AU 16 81352124 81352124 insertion of <=200bp - A intron_variant PACA-AU 16 81352528 81352528 single base substitution G A intron_variant PACA-AU 16 81354219 81354219 single base substitution A C intron_variant PACA-AU 16 81354255 81354257 deletion of <=200bp TTC - intron_variant PACA-AU 16 81356153 81356153 single base substitution A G intron_variant PACA-AU 16 81368270 81368275 deletion of <=200bp CACCCT - intron_variant PACA-AU 16 81380467 81380467 single base substitution C T intron_variant PACA-AU 16 81386892 81386892 single base substitution G A intron_variant PACA-AU 16 81392364 81392364 single base substitution G A intron_variant PACA-AU 16 81393016 81393016 single base substitution T G intron_variant PACA-AU 16 81394911 81394911 single base substitution T A intron_variant PACA-AU 16 81394911 81394911 single base substitution T A upstream_gene_variant PACA-AU 16 81400937 81400937 single base substitution G A intron_variant PACA-AU 16 81402607 81402607 single base substitution C T intron_variant PACA-AU 16 81406597 81406597 single base substitution C G downstream_gene_variant PACA-AU 16 81406597 81406597 single base substitution C G intron_variant PACA-AU 16 81410131 81410131 single base substitution C T downstream_gene_variant PACA-AU 16 81410131 81410131 single base substitution C T intron_variant PACA-AU 16 81410267 81410267 single base substitution G A downstream_gene_variant PACA-AU 16 81410267 81410267 single base substitution G A intron_variant PACA-AU 16 81410604 81410604 single base substitution C A downstream_gene_variant PACA-AU 16 81410604 81410604 single base substitution C A intron_variant PACA-AU 16 81414852 81414852 single base substitution A G 3_prime_UTR_variant PACA-AU 16 81418756 81418756 single base substitution G T 3_prime_UTR_variant PACA-AU 16 81418819 81418823 deletion of <=200bp TTGAC - 3_prime_UTR_variant PACA-AU 16 81420022 81420022 single base substitution G A 3_prime_UTR_variant PACA-AU 16 81422645 81422645 single base substitution G A 3_prime_UTR_variant PACA-AU 16 81424799 81424799 single base substitution T A downstream_gene_variant PACA-AU 16 81426636 81426636 single base substitution C T downstream_gene_variant PACA-AU 16 81428722 81428722 deletion of <=200bp C - downstream_gene_variant PACA-AU 16 81428732 81428732 single base substitution C T downstream_gene_variant PACA-CA 16 81344309 81344309 deletion of <=200bp T - upstream_gene_variant PACA-CA 16 81344827 81344827 single base substitution C T upstream_gene_variant PACA-CA 16 81345521 81345521 single base substitution A G upstream_gene_variant PACA-CA 16 81348590 81348590 single base substitution G A 5_prime_UTR_variant PACA-CA 16 81351126 81351126 single base substitution C T intron_variant PACA-CA 16 81351452 81351452 single base substitution T A intron_variant PACA-CA 16 81353244 81353244 insertion of <=200bp - A intron_variant PACA-CA 16 81359129 81359129 single base substitution T G intron_variant PACA-CA 16 81364831 81364831 single base substitution G T intron_variant PACA-CA 16 81367863 81367863 deletion of <=200bp G - intron_variant PACA-CA 16 81371720 81371720 single base substitution C T intron_variant PACA-CA 16 81373396 81373396 single base substitution C T intron_variant PACA-CA 16 81373538 81373538 single base substitution G A intron_variant PACA-CA 16 81379493 81379493 single base substitution A G intron_variant PACA-CA 16 81381632 81381632 single base substitution A T intron_variant PACA-CA 16 81382422 81382422 single base substitution G A intron_variant PACA-CA 16 81383944 81383944 single base substitution C T intron_variant PACA-CA 16 81387188 81387188 single base substitution G T intron_variant PACA-CA 16 81390726 81390726 single base substitution T A intron_variant PACA-CA 16 81395359 81395359 single base substitution G A intron_variant PACA-CA 16 81395359 81395359 single base substitution G A upstream_gene_variant PACA-CA 16 81397413 81397413 single base substitution C T synonymous_variant F367F 1101C>T PACA-CA 16 81397413 81397413 single base substitution C T upstream_gene_variant PACA-CA 16 81399761 81399761 single base substitution C T intron_variant PACA-CA 16 81402936 81402936 single base substitution C T intron_variant PACA-CA 16 81403352 81403352 single base substitution G A intron_variant PACA-CA 16 81405872 81405872 single base substitution A G downstream_gene_variant PACA-CA 16 81405872 81405872 single base substitution A G intron_variant PACA-CA 16 81406878 81406878 single base substitution T C downstream_gene_variant PACA-CA 16 81406878 81406878 single base substitution T C intron_variant PACA-CA 16 81407193 81407193 single base substitution A G downstream_gene_variant PACA-CA 16 81407193 81407193 single base substitution A G intron_variant PACA-CA 16 81407787 81407787 insertion of <=200bp - A downstream_gene_variant PACA-CA 16 81407787 81407787 insertion of <=200bp - A intron_variant PACA-CA 16 81408769 81408769 single base substitution G A downstream_gene_variant PACA-CA 16 81408769 81408769 single base substitution G A intron_variant PACA-CA 16 81412637 81412637 deletion of <=200bp A - 3_prime_UTR_variant PACA-CA 16 81417619 81417619 single base substitution A T 3_prime_UTR_variant PACA-CA 16 81420859 81420863 deletion of <=200bp AAAGT - 3_prime_UTR_variant PACA-CA 16 81422482 81422482 deletion of <=200bp T - 3_prime_UTR_variant PACA-CA 16 81423014 81423014 single base substitution A G 3_prime_UTR_variant PACA-CA 16 81423713 81423713 single base substitution T C 3_prime_UTR_variant PACA-CA 16 81426700 81426700 deletion of <=200bp T - downstream_gene_variant PACA-CA 16 81428301 81428301 single base substitution G A downstream_gene_variant PACA-CA 16 81428907 81428907 single base substitution C G downstream_gene_variant PAEN-IT 16 81373087 81373087 single base substitution A G intron_variant PBCA-DE 16 81346939 81346939 deletion of <=200bp A - upstream_gene_variant PBCA-DE 16 81362956 81362956 single base substitution C T intron_variant PBCA-DE 16 81372198 81372198 insertion of <=200bp - T intron_variant PBCA-DE 16 81391521 81391521 single base substitution G A missense_variant G320R 958G>A PBCA-DE 16 81393658 81393658 single base substitution G A intron_variant PBCA-DE 16 81405153 81405153 single base substitution G T intron_variant PBCA-DE 16 81410239 81410239 single base substitution A G downstream_gene_variant PBCA-DE 16 81410239 81410239 single base substitution A G intron_variant PBCA-DE 16 81410707 81410707 single base substitution A C intron_variant PBCA-DE 16 81418376 81418376 single base substitution C G 3_prime_UTR_variant PBCA-DE 16 81421578 81421578 single base substitution G A 3_prime_UTR_variant PBCA-DE 16 81423775 81423775 single base substitution G A 3_prime_UTR_variant PBCA-DE 16 81425096 81425096 single base substitution T C downstream_gene_variant PRAD-CA 16 81353811 81353811 single base substitution G C intron_variant PRAD-CA 16 81358427 81358427 single base substitution A C intron_variant PRAD-CA 16 81395289 81395289 single base substitution C G intron_variant PRAD-CA 16 81395289 81395289 single base substitution C G upstream_gene_variant PRAD-CA 16 81409213 81409213 single base substitution G C downstream_gene_variant PRAD-CA 16 81409213 81409213 single base substitution G C intron_variant PRAD-CA 16 81424599 81424599 single base substitution C T downstream_gene_variant PRAD-CA 16 81424675 81424675 single base substitution T C downstream_gene_variant PRAD-UK 16 81346541 81346541 single base substitution G A upstream_gene_variant PRAD-UK 16 81376932 81376932 single base substitution T A intron_variant PRAD-UK 16 81382541 81382541 single base substitution A T intron_variant PRAD-UK 16 81385282 81385282 single base substitution G T missense_variant D88Y 262G>T PRAD-UK 16 81388947 81388947 single base substitution A T intron_variant PRAD-UK 16 81412773 81412773 single base substitution G A 3_prime_UTR_variant PRAD-US 16 81390408 81390408 single base substitution A T missense_variant M218L 652A>T READ-US 16 81385245 81385245 single base substitution T C synonymous_variant L75L 225T>C RECA-EU 16 81345853 81345853 single base substitution T A upstream_gene_variant RECA-EU 16 81371330 81371330 single base substitution C T intron_variant RECA-EU 16 81371402 81371402 single base substitution A T intron_variant RECA-EU 16 81371984 81371984 single base substitution A T intron_variant RECA-EU 16 81373809 81373809 single base substitution G A intron_variant RECA-EU 16 81377121 81377121 single base substitution C A intron_variant RECA-EU 16 81390820 81390820 single base substitution C T intron_variant RECA-EU 16 81395215 81395215 single base substitution T A intron_variant RECA-EU 16 81395215 81395215 single base substitution T A upstream_gene_variant RECA-EU 16 81396358 81396358 single base substitution C T intron_variant RECA-EU 16 81396358 81396358 single base substitution C T upstream_gene_variant RECA-EU 16 81400441 81400441 single base substitution T G intron_variant RECA-EU 16 81405601 81405601 single base substitution C T exon_variant RECA-EU 16 81405601 81405601 single base substitution C T intron_variant RECA-EU 16 81407443 81407443 single base substitution G T downstream_gene_variant RECA-EU 16 81407443 81407443 single base substitution G T intron_variant RECA-EU 16 81409839 81409839 single base substitution T A downstream_gene_variant RECA-EU 16 81409839 81409839 single base substitution T A intron_variant RECA-EU 16 81426267 81426267 single base substitution G A downstream_gene_variant SKCA-BR 16 81350103 81350103 single base substitution C G intron_variant SKCA-BR 16 81350968 81350968 single base substitution T C intron_variant SKCA-BR 16 81352093 81352093 single base substitution C T intron_variant SKCA-BR 16 81358633 81358650 deletion of <=200bp CCAGGGATGGCTCCCAGG - intron_variant SKCA-BR 16 81370313 81370313 single base substitution G T intron_variant SKCA-BR 16 81370687 81370687 single base substitution C T intron_variant SKCA-BR 16 81370688 81370688 single base substitution C T intron_variant SKCA-BR 16 81372129 81372129 single base substitution C T intron_variant SKCA-BR 16 81373696 81373696 single base substitution C T intron_variant SKCA-BR 16 81374850 81374850 single base substitution C T intron_variant SKCA-BR 16 81377108 81377134 deletion of <=200bp CCAACGACAAAAACCACATGATTATCT - intron_variant SKCA-BR 16 81379385 81379385 single base substitution C T intron_variant SKCA-BR 16 81379985 81380004 deletion of <=200bp AGGCCTTAGGACTGGGCCAT - intron_variant SKCA-BR 16 81385887 81385887 single base substitution C T intron_variant SKCA-BR 16 81388251 81388251 single base substitution C T missense_variant P175L 524C>T SKCA-BR 16 81390666 81390666 single base substitution A G intron_variant SKCA-BR 16 81393019 81393019 insertion of <=200bp - TG intron_variant SKCA-BR 16 81393620 81393628 deletion of <=200bp TTGGATGGA - intron_variant SKCA-BR 16 81393658 81393658 single base substitution G A intron_variant SKCA-BR 16 81393776 81393776 single base substitution C T intron_variant SKCA-BR 16 81397750 81397750 single base substitution C T intron_variant SKCA-BR 16 81397750 81397750 single base substitution C T upstream_gene_variant SKCA-BR 16 81400127 81400127 single base substitution C T intron_variant SKCA-BR 16 81402957 81402957 single base substitution C T intron_variant SKCA-BR 16 81407722 81407722 single base substitution C T downstream_gene_variant SKCA-BR 16 81407722 81407722 single base substitution C T intron_variant SKCA-BR 16 81410236 81410248 deletion of <=200bp CATATATGTGTGT - downstream_gene_variant SKCA-BR 16 81410236 81410248 deletion of <=200bp CATATATGTGTGT - intron_variant SKCA-BR 16 81412657 81412657 single base substitution C T 3_prime_UTR_variant SKCA-BR 16 81414917 81414917 single base substitution C A 3_prime_UTR_variant SKCA-BR 16 81418970 81418970 single base substitution C T 3_prime_UTR_variant SKCA-BR 16 81421278 81421278 single base substitution G A 3_prime_UTR_variant SKCA-BR 16 81424117 81424117 single base substitution G A 3_prime_UTR_variant SKCA-BR 16 81424588 81424588 insertion of <=200bp - CACTGCCTGAGCCTCTTCCATCGCTG downstream_gene_variant SKCA-BR 16 81424627 81424627 insertion of <=200bp - CT downstream_gene_variant SKCA-BR 16 81424648 81424648 single base substitution T C downstream_gene_variant SKCA-BR 16 81424651 81424651 insertion of <=200bp - CT downstream_gene_variant SKCA-BR 16 81424696 81424696 single base substitution C T downstream_gene_variant SKCA-BR 16 81427526 81427526 insertion of <=200bp - GTCTT downstream_gene_variant SKCM-US 16 81398669 81398669 single base substitution C T missense_variant P443S 1327C>T SKCM-US 16 81398669 81398669 single base substitution C T upstream_gene_variant SKCM-US 16 81399011 81399011 single base substitution G A missense_variant R477Q 1430G>A SKCM-US 16 81399011 81399011 single base substitution G A upstream_gene_variant SKCM-US 16 81411074 81411074 single base substitution A C missense_variant H556P 1667A>C SKCM-US 16 81411177 81411177 single base substitution C T synonymous_variant F590F 1770C>T STAD-US 16 81388112 81388112 single base substitution A G missense_variant I129V 385A>G STAD-US 16 81388220 81388220 single base substitution A G missense_variant S165G 493A>G STAD-US 16 81390507 81390507 single base substitution A G missense_variant I251V 751A>G STAD-US 16 81398592 81398592 single base substitution C T missense_variant A417V 1250C>T STAD-US 16 81398592 81398592 single base substitution C T upstream_gene_variant STAD-US 16 81398967 81398967 single base substitution G A synonymous_variant V462V 1386G>A STAD-US 16 81398967 81398967 single base substitution G A upstream_gene_variant STAD-US 16 81399002 81399002 single base substitution G T missense_variant G474V 1421G>T STAD-US 16 81399002 81399002 single base substitution G T upstream_gene_variant STAD-US 16 81399030 81399030 single base substitution G A exon_variant STAD-US 16 81399030 81399030 single base substitution G A synonymous_variant Q483Q 1449G>A STAD-US 16 81410860 81410860 single base substitution C T synonymous_variant P513P 1539C>T STAD-US 16 81411130 81411130 single base substitution A G missense_variant I575V 1723A>G UCEC-US 16 81385256 81385256 single base substitution C T missense_variant S79L 236C>T UCEC-US 16 81385286 81385286 single base substitution A G missense_variant Y89C 266A>G UCEC-US 16 81390393 81390393 single base substitution C A missense_variant H213N 637C>A UCEC-US 16 81390524 81390524 single base substitution G A synonymous_variant P256P 768G>A UCEC-US 16 81390594 81390596 deletion of <=200bp GGA - inframe_deletion G280 UCEC-US 16 81391484 81391484 single base substitution C T synonymous_variant I307I 921C>T UCEC-US 16 81397413 81397413 single base substitution C T synonymous_variant F367F 1101C>T UCEC-US 16 81397413 81397413 single base substitution C T upstream_gene_variant UCEC-US 16 81398611 81398611 single base substitution C A synonymous_variant I423I 1269C>A UCEC-US 16 81398611 81398611 single base substitution C A upstream_gene_variant UCEC-US 16 81398614 81398614 single base substitution C T synonymous_variant Y424Y 1272C>T UCEC-US 16 81398614 81398614 single base substitution C T upstream_gene_variant UCEC-US 16 81411040 81411040 single base substitution C T missense_variant R545C 1633C>T UCEC-US 16 81411106 81411106 single base substitution C T missense_variant R567C 1699C>T UCEC-US 16 81411177 81411177 single base substitution C T synonymous_variant F590F 1770C>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand PTC-14C COSM4129402 c.1281T>C p.G427G Substitution - coding silent 16:81365018-81365018 + PCSI_0062_Pa_X COSM275260 c.1101C>T p.F367F Substitution - coding silent 16:81363808-81363808 + 587376 COSM1207901 c.548C>A p.S183Y Substitution - Missense 16:81354670-81354670 + TCGA-D1-A103-01 COSM974093 c.1272C>T p.Y424Y Substitution - coding silent 16:81365009-81365009 + TCGA-AP-A059-01 COSM974095 c.1699C>T p.R567C Substitution - Missense 16:81377501-81377501 + TCGA-D1-A103-01 COSM974096 c.1770C>T p.F590F Substitution - coding silent 16:81377572-81377572 + DLD1 COSM4623427 c.28C>A p.P10T Substitution - Missense 16:81315141-81315141 + TCGA-CG-5728-01 COSM4063103 c.1386G>A p.V462V Substitution - coding silent 16:81365362-81365362 + TCGA-CK-5913-01 COSM1380078 c.1182C>T p.Y394Y Substitution - coding silent 16:81363889-81363889 + TCGA-CM-6161-01 COSM1380079 c.1589A>T p.Y530F Substitution - Missense 16:81377305-81377305 + SNB19 COSM1679298 c.1752G>T p.Q584H Substitution - Missense 16:81377554-81377554 + TCGA-D3-A2JA-06 COSM3889043 c.1667A>C p.H556P Substitution - Missense 16:81377469-81377469 + PTC-7C COSM3755118 c.1293C>T p.Y431Y Substitution - coding silent 16:81365030-81365030 + TCGA-FP-A4BE-01 COSM4063104 c.1421G>T p.G474V Substitution - Missense 16:81365397-81365397 + BD152T COSM5507055 c.1606G>A p.D536N Substitution - Missense 16:81377322-81377322 + LUAD-2GUGK COSM400519 c.401G>C p.C134S Substitution - Missense 16:81354523-81354523 + ESCC_BICR_035T COSM5429429 c.1084G>A p.E362K Substitution - Missense 16:81362609-81362609 + TCGA-JW-A5VL-01 COSM4847426 c.109G>C p.D37H Substitution - Missense 16:81315222-81315222 + U373 COSM1679298 c.1752G>T p.Q584H Substitution - Missense 16:81377554-81377554 + OSCC-GB_01170111 COSM1380074 c.334C>T p.L112L Substitution - coding silent 16:81354456-81354456 + TCGA-AA-3672-01 COSM266574 c.877C>T p.R293* Substitution - Nonsense 16:81357835-81357835 + TCGA-A4-7585-01 COSM3988688 c.1696C>T p.R566C Substitution - Missense 16:81377498-81377498 + TCGA-BP-4347-01 COSM3361926 c.1660T>G p.W554G Substitution - Missense 16:81377462-81377462 + T3090 COSM4686377 c.244G>T p.V82F Substitution - Missense 16:81351659-81351659 + TCGA-AP-A051-01 COSM974092 c.1269C>A p.I423I Substitution - coding silent 16:81365006-81365006 + Patient_1 COSM5414147 c.697G>A p.E233K Substitution - Missense 16:81356848-81356848 + TCGA-A6-5665-01 COSM1380076 c.782C>T p.A261V Substitution - Missense 16:81356933-81356933 + 227_T COSM3957865 c.427C>T p.H143Y Substitution - Missense 16:81354549-81354549 + H2171 COSM311372 c.777G>A p.G259G Substitution - coding silent 16:81356928-81356928 + TCGA-12-1597-01 COSM3402504 c.779A>G p.E260G Substitution - Missense 16:81356930-81356930 + HCC170T COSM3717100 c.977G>T p.G326V Substitution - Missense 16:81362502-81362502 + TCGA-AM-5820-01 COSM3691197 c.1374-1G>T p.? Unknown 16:81365349-81365349 + TCGA-D5-6928-01 COSM1380074 c.334C>T p.L112L Substitution - coding silent 16:81354456-81354456 + TCGA-A2-A0T6-01 COSM435833 c.1169C>A p.S390Y Substitution - Missense 16:81363876-81363876 + TCGA-AP-A05N-01 COSM974091 c.838_840delGGA p.G280delG Deletion - In frame 16:81356989-81356991 + T3021 COSM4686380 c.843_844delAG p.R283fs*17 Deletion - Frameshift 16:81356994-81356995 + 585267 COSM320548 c.790G>T p.A264S Substitution - Missense 16:81356941-81356941 + HF-19967 COSM1192986 c.1361_1362insA p.E456fs*25 Insertion - Frameshift 16:81365098-81365099 + TCGA-AA-3492-01 COSM1380075 c.444C>T p.H148H Substitution - coding silent 16:81354566-81354566 + TCGA-CD-8536-01 COSM4063106 c.1539C>T p.P513P Substitution - coding silent 16:81377255-81377255 + TCGA-E9-A54X-01 COSM3818611 c.878G>A p.R293Q Substitution - Missense 16:81357836-81357836 + TCGA-BR-8372-01 COSM4063099 c.385A>G p.I129V Substitution - Missense 16:81354507-81354507 + TCGA-CD-A4MG-01 COSM4063100 c.493A>G p.S165G Substitution - Missense 16:81354615-81354615 + EGC3 COSM974087 c.236C>T p.S79L Substitution - Missense 16:81351651-81351651 + QC2-22-T2 COSM5653060 c.146C>A p.A49E Substitution - Missense 16:81315259-81315259 + KM12 COSM1679297 c.724C>T p.R242* Substitution - Nonsense 16:81356875-81356875 + T1240 COSM4686378 c.694C>T p.R232W Substitution - Missense 16:81356845-81356845 + TCGA-G9-7510-01 COSM1470921 c.652A>T p.M218L Substitution - Missense 16:81356803-81356803 + sysucc-1370T COSM5470577 c.725G>A p.R242Q Substitution - Missense 16:81356876-81356876 + TCGA-CA-6718-01 COSM1207901 c.548C>A p.S183Y Substitution - Missense 16:81354670-81354670 + CSCC-49-T COSM4521642 c.1121G>A p.G374E Substitution - Missense 16:81363828-81363828 + HCC170 COSM3717100 c.977G>T p.G326V Substitution - Missense 16:81362502-81362502 + S02209 COSM5675183 c.1745G>T p.R582L Substitution - Missense 16:81377547-81377547 + C086 COSM5531612 c.1289C>T p.S430F Substitution - Missense 16:81365026-81365026 + TCGA-F5-6814-01 COSM3421189 c.225T>C p.L75L Substitution - coding silent 16:81351640-81351640 + PT38 COSM5923142 c.1366G>A p.E456K Substitution - Missense 16:81365103-81365103 + T595 COSM4686379 c.755C>T p.P252L Substitution - Missense 16:81356906-81356906 + TCGA-AP-A059-01 COSM974090 c.768G>A p.P256P Substitution - coding silent 16:81356919-81356919 + TCGA-AP-A056-01 COSM974088 c.266A>G p.Y89C Substitution - Missense 16:81351681-81351681 + TCGA-B2-3923-01 COSM1493811 c.968C>A p.S323* Substitution - Nonsense 16:81357926-81357926 + TCGA-24-1464-01 COSM74728 c.218T>C p.I73T Substitution - Missense 16:81351633-81351633 + STC297 COSM5055128 c.944C>T p.P315L Substitution - Missense 16:81357902-81357902 + TCGA-AA-A00N-01 COSM275260 c.1101C>T p.F367F Substitution - coding silent 16:81363808-81363808 + U251 COSM1679298 c.1752G>T p.Q584H Substitution - Missense 16:81377554-81377554 + 1517_PT COSM5754923 c.461C>T p.T154I Substitution - Missense 16:81354583-81354583 + Pat_41_B COSM5851568 c.1382C>T p.A461V Substitution - Missense 16:81365358-81365358 + LUAD-CHTN-MAD06-00668 COSM359036 c.1565C>A p.A522D Substitution - Missense 16:81377281-81377281 + Pat_76_A COSM74729 c.857G>A p.R286Q Substitution - Missense 16:81357815-81357815 + YUMOBER COSM5385456 c.1349C>T p.A450V Substitution - Missense 16:81365086-81365086 + TCGA-JW-A69B-01 COSM4829559 c.1646G>T p.R549I Substitution - Missense 16:81377448-81377448 + Pat_45_B COSM5851567 c.505G>A p.E169K Substitution - Missense 16:81354627-81354627 + TCGA-D1-A0ZO-01 COSM974094 c.1633C>T p.R545C Substitution - Missense 16:81377435-81377435 + T3436 COSM4686376 c.72C>T p.R24R Substitution - coding silent 16:81315185-81315185 + TCGA-K7-A6G5-01 COSM4939325 c.661C>T p.L221L Substitution - coding silent 16:81356812-81356812 + ICGC_MB24 COSM215662 c.958G>A p.G320R Substitution - Missense 16:81357916-81357916 + CLL065 COSM1290598 c.1021C>G p.L341V Substitution - Missense 16:81362546-81362546 + BD176T COSM5494912 c.744T>C p.C248C Substitution - coding silent 16:81356895-81356895 + TCGA-BR-8058-01 COSM4063105 c.1449G>A p.Q483Q Substitution - coding silent 16:81365425-81365425 + TCGA-EE-A3JD-06 COSM1207899 c.1430G>A p.R477Q Substitution - Missense 16:81365406-81365406 + CSCC-27-T COSM4540676 c.287G>A p.R96K Substitution - Missense 16:81354409-81354409 + ESCC_BICR_071T COSM4433818 c.1540G>A p.A514T Substitution - Missense 16:81377256-81377256 + SC_9096 COSM5550184 c.1727C>T p.A576V Substitution - Missense 16:81377529-81377529 + TCGA-BS-A0TC-01 COSM177211 c.921C>T p.I307I Substitution - coding silent 16:81357879-81357879 + 478 COSM4438941 c.679G>T p.D227Y Substitution - Missense 16:81356830-81356830 + CSCC-27-T COSM4568200 c.1022T>G p.L341R Substitution - Missense 16:81362547-81362547 + CSCC-46-T COSM4451881 c.1464A>G p.V488V Substitution - coding silent 16:81365440-81365440 + TCGA-BR-6566-01 COSM4063102 c.1250C>T p.A417V Substitution - Missense 16:81364987-81364987 + TCGA-AM-5820-01 COSM3755118 c.1293C>T p.Y431Y Substitution - coding silent 16:81365030-81365030 + TCGA-HJ-7597-01 COSM4063101 c.751A>G p.I251V Substitution - Missense 16:81356902-81356902 + PT49 COSM5851569 c.1435C>T p.R479C Substitution - Missense 16:81365411-81365411 + TCGA-AA-3715-01 COSM266574 c.877C>T p.R293* Substitution - Nonsense 16:81357835-81357835 + Au1 COSM5596764 c.484C>T p.R162* Substitution - Nonsense 16:81354606-81354606 + TCGA-18-3414-01 COSM704640 c.1121G>T p.G374V Substitution - Missense 16:81363828-81363828 + BD154T COSM5055128 c.944C>T p.P315L Substitution - Missense 16:81357902-81357902 + Pat_46_B COSM5851570 c.1790C>T p.P597L Substitution - Missense 16:81377592-81377592 + AOCS-137-1-X COSM4141920 c.526C>A p.Q176K Substitution - Missense 16:81354648-81354648 + Mel18 COSM3727465 c.500delC p.T167fs*5 Deletion - Frameshift 16:81354622-81354622 + TCGA-CG-5721-01 COSM4063107 c.1723A>G p.I575V Substitution - Missense 16:81377525-81377525 + 9227_T COSM5039718 c.407G>A p.G136D Substitution - Missense 16:81354529-81354529 + 587350 COSM1207899 c.1430G>A p.R477Q Substitution - Missense 16:81365406-81365406 + PTC-7C COSM974092 c.1269C>A p.I423I Substitution - coding silent 16:81365006-81365006 + Pat_41_A COSM5851569 c.1435C>T p.R479C Substitution - Missense 16:81365411-81365411 + RH30SJ_ COSM974087 c.236C>T p.S79L Substitution - Missense 16:81351651-81351651 + TCGA-AP-A059-01 COSM974089 c.637C>A p.H213N Substitution - Missense 16:81356788-81356788 + 435 COSM4433818 c.1540G>A p.A514T Substitution - Missense 16:81377256-81377256 + TCGA-CZ-4865-01 COSM3361925 c.1263G>T p.K421N Substitution - Missense 16:81365000-81365000 + KM12 COSM1679297 c.724C>T p.R242* Substitution - Nonsense 16:81356875-81356875 + XHDG02 COSM4767873 c.1383G>A p.A461A Substitution - coding silent 16:81365359-81365359 + TCGA-AA-A010-01 COSM281313 c.1777C>T p.R593C Substitution - Missense 16:81377579-81377579 + TCGA-GN-A26C-01 COSM3512718 c.1327C>T p.P443S Substitution - Missense 16:81365064-81365064 + TCGA-BS-A0UV-01 COSM974087 c.236C>T p.S79L Substitution - Missense 16:81351651-81351651 + TCGA-AN-A046-01 COSM2693293 c.922G>A p.E308K Substitution - Missense 16:81357880-81357880 + TCGA-23-1022-01 COSM74729 c.857G>A p.R286Q Substitution - Missense 16:81357815-81357815 + LP6005500-DNA_G03 COSM5035129 c.1432A>C p.S478R Substitution - Missense 16:81365408-81365408 + AOCS-137-3-7 COSM4141920 c.526C>A p.Q176K Substitution - Missense 16:81354648-81354648 + 2521243 COSM5886916 c.1239C>T p.I413I Substitution - coding silent 16:81364976-81364976 + TCGA-DA-A3F8-06 COSM974096 c.1770C>T p.F590F Substitution - coding silent 16:81377572-81377572 + LUAD-S01357 COSM386759 c.1436G>T p.R479L Substitution - Missense 16:81365412-81365412 + 587342 COSM1207900 c.9G>T p.E3D Substitution - Missense 16:81315122-81315122 + TCGA-AP-A056-01 COSM275260 c.1101C>T p.F367F Substitution - coding silent 16:81363808-81363808 + TCGA-CW-5588-01 COSM472163 c.1167T>C p.I389I Substitution - coding silent 16:81363874-81363874 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.112569 16q24.1 605379

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.H556P c.1667A>C 16 81411074 CM A G 3-UTRSNV . c.1791+172A>G 16 81411370 CM A G IntronicSNV . c.1503-1363A>G 16 81409461 CLL A G Missense p.E260G c.779A>G 16 81390535 GBM A G Missense p.K287R c.860A>G 16 81391423 LUAD A T Missense p.M218L c.652A>T 16 81390408 PRAD C A 3-UTRSNV . c.1791+80C>A 16 81411278 CM C A Missense p.S390Y c.1169C>A 16 81397481 BRCA C G Missense p.L341V c.1021C>G 16 81396151 CLL C G Missense p.Q176E c.526C>G 16 81388253 HNSC C T Missense p.P443S c.1327C>T 16 81398669 CM C T Missense p.P562L c.1685C>T 16 81411092 CM C T Missense p.R479C c.1435C>T 16 81399016 CM C T Missense p.R545C c.1633C>T 16 81411040 UCEC C T Missense p.T489I c.1466C>T 16 81399047 HNSC C T Synonymous p.F590F c.1770C>T 16 81411177 CM C T Synonymous p.I307I c.921C>T 16 81391484 UCEC G A Missense p.C145Y c.434G>A 16 81388161 COREAD G A Missense p.G320R c.958G>A 16 81391521 MB G A Missense p.R286Q c.857G>A 16 81391420 OV G A Missense p.R477Q c.1430G>A 16 81399011 CM G A Missense p.S528N c.1583G>A 16 81410904 CM G A Synonymous p.V462V c.1386G>A 16 81398967 STAD G C SpliceDonorSNV . c.1612+1G>C 16 81410934 LUAD GGA - InFrameDeletion p.G280delG c.839_841delGAG 16 81390594 UCEC - G IntronicInsertion . c.1373+16dupG 16 81398729 STAD G T Missense p.A264S c.790G>T 16 81390546 SCLC G T Missense p.G374V c.1121G>T 16 81397433 LUSC G T Missense p.K421N c.1263G>T 16 81398605 RCCC G T Missense p.V189F c.565G>T 16 81388292 LUAD G T Synonymous p.L157L c.471G>T 16 81388198 LUAD G T Synonymous p.P252P c.756G>T 16 81390512 LUAD G T Synonymous p.R269R c.807G>T 16 81390563 STAD T A 3-UTRSNV . c.1791+2326T>A 16 81413524 DLBCL T A Synonymous p.I378I c.1134T>A 16 81397446 CM T C IntronicSNV . c.167+1138T>C 16 81350023 PIA T C Missense p.I73T c.218T>C 16 81385238 OV T G Missense p.W554G c.1660T>G 16 81411067 RCCC