Mutation - TCGA |
Type | Chromosome | Start Position | End Position | Strand | Variant Classification | Variant Type | Reference Allele | Tumor_seq Allele 1 | Tumor_seq Allele 2 | Tumor Sample Barcode | Matched Norm Sample Barcode | Genome Change | cDNA Change | Codon Change | Protein Change |
ACC | 3 | 114070578 | 114070578 | + | Missense_Mutation | SNP | C | C | T | TCGA-OR-A5K4-01A-11D-A29I-10 | TCGA-OR-A5K4-10A-01D-A29L-10 | g.chr3:114070578C>T | c.347G>A | c.(346-348)cGc>cAc | p.R116H |
BLCA | 3 | 114057927 | 114057927 | + | Missense_Mutation | SNP | G | G | C | TCGA-FD-A6TB-01A-12D-A339-08 | TCGA-FD-A6TB-10A-21D-A339-08 | g.chr3:114057927G>C | c.2151C>G | c.(2149-2151)tgC>tgG | p.C717W |
BLCA | 3 | 114069470 | 114069470 | + | Silent | SNP | G | G | A | TCGA-DK-AA77-01A-11D-A391-08 | TCGA-DK-AA77-10A-01D-A394-08 | g.chr3:114069470G>A | c.1455C>T | c.(1453-1455)agC>agT | p.S485S |
BLCA | 3 | 114069542 | 114069542 | + | Silent | SNP | C | C | T | TCGA-2F-A9KW-01A-11D-A38G-08 | TCGA-2F-A9KW-10A-01D-A38J-08 | g.chr3:114069542C>T | c.1383G>A | c.(1381-1383)tcG>tcA | p.S461S |
BLCA | 3 | 114069835 | 114069835 | + | Missense_Mutation | SNP | C | C | T | TCGA-DK-A3X1-01A-12D-A22Z-08 | TCGA-DK-A3X1-10A-01D-A22Z-08 | g.chr3:114069835C>T | c.1090G>A | c.(1090-1092)Gag>Aag | p.E364K |
BLCA | 3 | 114070334 | 114070334 | + | Silent | SNP | C | C | T | TCGA-DK-A3IT-01A-31D-A20D-08 | TCGA-DK-A3IT-10A-01D-A20D-08 | g.chr3:114070334C>T | c.591G>A | c.(589-591)gtG>gtA | p.V197V |
BLCA | 3 | 114070467 | 114070467 | + | Missense_Mutation | SNP | T | T | C | TCGA-GV-A3QI-01A-11D-A21Z-08 | TCGA-GV-A3QI-10A-01D-A21Z-08 | g.chr3:114070467T>C | c.458A>G | c.(457-459)aAg>aGg | p.K153R |
BLCA | 3 | 114070607 | 114070607 | + | Silent | SNP | T | T | C | TCGA-ZF-AA4W-01A-12D-A38G-08 | TCGA-ZF-AA4W-10A-01D-A38J-08 | g.chr3:114070607T>C | c.318A>G | c.(316-318)gtA>gtG | p.V106V |
BRCA | 3 | 114057923 | 114057923 | + | Missense_Mutation | SNP | C | C | T | TCGA-D8-A1Y1-01A-21D-A14K-09 | TCGA-D8-A1Y1-10A-01D-A14K-09 | g.chr3:114057923C>T | c.2155G>A | c.(2155-2157)Gtc>Atc | p.V719I |
BRCA | 3 | 114058003 | 114058003 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-AN-A0AK-01A-21W-A019-09 | TCGA-AN-A0AK-10A-01W-A021-09 | g.chr3:114058003delG | c.2075delC | c.(2074-2076)cctfs | p.P692fs |
BRCA | 3 | 114069805 | 114069805 | + | Missense_Mutation | SNP | T | T | G | TCGA-BH-A18Q-01A-12D-A12B-09 | TCGA-BH-A18Q-11A-34D-A12B-09 | g.chr3:114069805T>G | c.1120A>C | c.(1120-1122)Agc>Cgc | p.S374R |
BRCA | 3 | 114069881 | 114069881 | + | Silent | SNP | C | C | T | TCGA-EW-A1PD-01A-11D-A142-09 | TCGA-EW-A1PD-10A-01D-A142-09 | g.chr3:114069881C>T | c.1044G>A | c.(1042-1044)ctG>ctA | p.L348L |
BRCA | 3 | 114070183 | 114070183 | + | Missense_Mutation | SNP | A | A | T | TCGA-AC-A5EI-01A-11D-A27P-09 | TCGA-AC-A5EI-10A-01D-A27P-09 | g.chr3:114070183A>T | c.742T>A | c.(742-744)Tac>Aac | p.Y248N |
CESC | 3 | 114057933 | 114057933 | + | Silent | SNP | G | G | A | TCGA-JW-A5VL-01A-11D-A28B-09 | TCGA-JW-A5VL-10A-01D-A28E-09 | g.chr3:114057933G>A | c.2145C>T | c.(2143-2145)taC>taT | p.Y715Y |
CESC | 3 | 114069161 | 114069161 | + | Silent | SNP | G | G | A | TCGA-FU-A3WB-01A-11D-A22X-09 | TCGA-FU-A3WB-10A-01D-A22X-09 | g.chr3:114069161G>A | c.1764C>T | c.(1762-1764)acC>acT | p.T588T |
CESC | 3 | 114069347 | 114069347 | + | Missense_Mutation | SNP | G | G | C | TCGA-JW-A5VL-01A-11D-A28B-09 | TCGA-JW-A5VL-10A-01D-A28E-09 | g.chr3:114069347G>C | c.1578C>G | c.(1576-1578)ttC>ttG | p.F526L |
COAD | 3 | 114057990 | 114057990 | + | Silent | SNP | G | G | T | TCGA-AU-6004-01A-11D-1719-10 | TCGA-AU-6004-10A-01D-1719-10 | g.chr3:114057990G>T | c.2088C>A | c.(2086-2088)ccC>ccA | p.P696P |
COAD | 3 | 114057991 | 114057991 | + | Missense_Mutation | SNP | G | G | T | TCGA-AY-6197-01A-11D-1719-10 | TCGA-AY-6197-10A-01D-1719-10 | g.chr3:114057991G>T | c.2087C>A | c.(2086-2088)cCc>cAc | p.P696H |
COAD | 3 | 114058003 | 114058003 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-A6-5661-01A-01D-1650-10 | TCGA-A6-5661-10A-01D-1650-10 | g.chr3:114058003delG | c.2075delC | c.(2074-2076)cctfs | p.P692fs |
COAD | 3 | 114058003 | 114058003 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-A6-6653-01A-11D-1771-10 | TCGA-A6-6653-10A-01D-1771-10 | g.chr3:114058003delG | c.2075delC | c.(2074-2076)cctfs | p.P692fs |
COAD | 3 | 114058003 | 114058003 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-AA-3672-01A-01W-0900-09 | TCGA-AA-3672-10A-01W-0900-09 | g.chr3:114058003delG | c.2075delC | c.(2074-2076)cctfs | p.P692fs |
COAD | 3 | 114058003 | 114058003 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-AA-3815-01A-01W-0995-10 | TCGA-AA-3815-10A-01W-0995-10 | g.chr3:114058003delG | c.2075delC | c.(2074-2076)cctfs | p.P692fs |
COAD | 3 | 114058003 | 114058003 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-AA-3950-01A-02W-0995-10 | TCGA-AA-3950-10A-01W-0995-10 | g.chr3:114058003delG | c.2075delC | c.(2074-2076)cctfs | p.P692fs |
COAD | 3 | 114058003 | 114058003 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-AY-6197-01A-11D-1719-10 | TCGA-AY-6197-10A-01D-1719-10 | g.chr3:114058003delG | c.2075delC | c.(2074-2076)cctfs | p.P692fs |
COAD | 3 | 114058003 | 114058003 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-CK-5913-01A-11D-1650-10 | TCGA-CK-5913-10A-01D-1650-10 | g.chr3:114058003delG | c.2075delC | c.(2074-2076)cctfs | p.P692fs |
COAD | 3 | 114058003 | 114058003 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-CK-5916-01A-11D-1650-10 | TCGA-CK-5916-10A-01D-1650-10 | g.chr3:114058003delG | c.2075delC | c.(2074-2076)cctfs | p.P692fs |
COAD | 3 | 114058003 | 114058003 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-CM-6171-01A-11D-1650-10 | TCGA-CM-6171-10A-01D-1650-10 | g.chr3:114058003delG | c.2075delC | c.(2074-2076)cctfs | p.P692fs |
COAD | 3 | 114058003 | 114058003 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-F4-6570-01A-11D-1771-10 | TCGA-F4-6570-10A-01D-1771-10 | g.chr3:114058003delG | c.2075delC | c.(2074-2076)cctfs | p.P692fs |
COAD | 3 | 114058003 | 114058003 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-F4-6856-01A-11D-1924-10 | TCGA-F4-6856-10A-01D-1924-10 | g.chr3:114058003delG | c.2075delC | c.(2074-2076)cctfs | p.P692fs |
COAD | 3 | 114058003 | 114058003 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr3:114058003delG | c.2075delC | c.(2074-2076)cctfs | p.P692fs |
COAD | 3 | 114058003 | 114058004 | + | Frame_Shift_Del | DEL | GG | GG | - | TCGA-A6-6780-01A-11D-1835-10 | TCGA-A6-6780-10A-01D-1835-10 | g.chr3:114058003_114058004delGG | c.2074_2075delCC | c.(2074-2076)cctfs | p.P692fs |
COAD | 3 | 114058003 | 114058004 | + | Frame_Shift_Del | DEL | GG | GG | - | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr3:114058003_114058004delGG | c.2074_2075delCC | c.(2074-2076)cctfs | p.P692fs |
COAD | 3 | 114058037 | 114058037 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3966-01A-01W-1073-09 | TCGA-AA-3966-10A-01W-1073-09 | g.chr3:114058037C>T | c.2041G>A | c.(2041-2043)Gtg>Atg | p.V681M |
COAD | 3 | 114058138 | 114058138 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3845-01A-01W-0995-10 | TCGA-AA-3845-10A-01W-0995-10 | g.chr3:114058138C>A | c.1940G>T | c.(1939-1941)aGc>aTc | p.S647I |
COAD | 3 | 114069325 | 114069325 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-6922-01A-11D-1924-10 | TCGA-D5-6922-10A-01D-1924-10 | g.chr3:114069325C>T | c.1600G>A | c.(1600-1602)Ggc>Agc | p.G534S |
COAD | 3 | 114069416 | 114069416 | + | Silent | SNP | A | A | G | TCGA-D5-6923-01A-11D-1924-10 | TCGA-D5-6923-10A-01D-1924-10 | g.chr3:114069416A>G | c.1509T>C | c.(1507-1509)gcT>gcC | p.A503A |
COAD | 3 | 114069732 | 114069732 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3815-01A-01W-0995-10 | TCGA-AA-3815-10A-01W-0995-10 | g.chr3:114069732G>A | c.1193C>T | c.(1192-1194)gCg>gTg | p.A398V |
COAD | 3 | 114069890 | 114069890 | + | Silent | SNP | C | C | T | TCGA-CM-6170-01A-11D-1650-10 | TCGA-CM-6170-10A-01D-1650-10 | g.chr3:114069890C>T | c.1035G>A | c.(1033-1035)gtG>gtA | p.V345V |
COAD | 3 | 114069891 | 114069891 | + | Missense_Mutation | SNP | A | A | G | TCGA-D5-6538-01A-11D-1719-10 | TCGA-D5-6538-10A-01D-1719-10 | g.chr3:114069891A>G | c.1034T>C | c.(1033-1035)gTg>gCg | p.V345A |
COAD | 3 | 114069901 | 114069901 | + | Missense_Mutation | SNP | G | G | T | TCGA-CK-6746-01A-11D-1835-10 | TCGA-CK-6746-10A-01D-1835-10 | g.chr3:114069901G>T | c.1024C>A | c.(1024-1026)Cag>Aag | p.Q342K |
COAD | 3 | 114069920 | 114069920 | + | Silent | SNP | G | G | A | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr3:114069920G>A | c.1005C>T | c.(1003-1005)gaC>gaT | p.D335D |
COAD | 3 | 114070037 | 114070037 | + | Silent | SNP | C | C | T | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr3:114070037C>T | c.888G>A | c.(886-888)caG>caA | p.Q296Q |
COAD | 3 | 114070275 | 114070275 | + | Missense_Mutation | SNP | T | T | C | TCGA-AD-6964-01A-11D-1924-10 | TCGA-AD-6964-10A-01D-1924-10 | g.chr3:114070275T>C | c.650A>G | c.(649-651)gAg>gGg | p.E217G |
COAD | 3 | 114070331 | 114070331 | + | Silent | SNP | G | G | A | TCGA-AA-3947-01A-01W-0995-10 | TCGA-AA-3947-10A-01W-0995-10 | g.chr3:114070331G>A | c.594C>T | c.(592-594)ggC>ggT | p.G198G |
COAD | 3 | 114070445 | 114070445 | + | Silent | SNP | G | G | A | TCGA-AA-A022-01A-21W-A096-10 | TCGA-AA-A022-11A-11W-A096-10 | g.chr3:114070445G>A | c.480C>T | c.(478-480)agC>agT | p.S160S |
COAD | 3 | 114070511 | 114070511 | + | Silent | SNP | G | G | A | TCGA-AZ-6601-01A-11D-1771-10 | TCGA-AZ-6601-11A-01D-1771-10 | g.chr3:114070511G>A | c.414C>T | c.(412-414)agC>agT | p.S138S |
COADREAD | 3 | 114057990 | 114057990 | + | Silent | SNP | G | G | T | TCGA-AU-6004-01A-11D-1719-10 | TCGA-AU-6004-10A-01D-1719-10 | g.chr3:114057990G>T | c.2088C>A | c.(2086-2088)ccC>ccA | p.P696P |
COADREAD | 3 | 114057991 | 114057991 | + | Missense_Mutation | SNP | G | G | T | TCGA-AY-6197-01A-11D-1719-10 | TCGA-AY-6197-10A-01D-1719-10 | g.chr3:114057991G>T | c.2087C>A | c.(2086-2088)cCc>cAc | p.P696H |
COADREAD | 3 | 114058003 | 114058003 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-A6-5661-01A-01D-1650-10 | TCGA-A6-5661-10A-01D-1650-10 | g.chr3:114058003delG | c.2075delC | c.(2074-2076)cctfs | p.P692fs |
COADREAD | 3 | 114058003 | 114058003 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-A6-6653-01A-11D-1771-10 | TCGA-A6-6653-10A-01D-1771-10 | g.chr3:114058003delG | c.2075delC | c.(2074-2076)cctfs | p.P692fs |
COADREAD | 3 | 114058003 | 114058003 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-AA-3672-01A-01W-0900-09 | TCGA-AA-3672-10A-01W-0900-09 | g.chr3:114058003delG | c.2075delC | c.(2074-2076)cctfs | p.P692fs |
COADREAD | 3 | 114058003 | 114058003 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-AA-3815-01A-01W-0995-10 | TCGA-AA-3815-10A-01W-0995-10 | g.chr3:114058003delG | c.2075delC | c.(2074-2076)cctfs | p.P692fs |
COADREAD | 3 | 114058003 | 114058003 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-AA-3950-01A-02W-0995-10 | TCGA-AA-3950-10A-01W-0995-10 | g.chr3:114058003delG | c.2075delC | c.(2074-2076)cctfs | p.P692fs |
COADREAD | 3 | 114058003 | 114058003 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-AY-6197-01A-11D-1719-10 | TCGA-AY-6197-10A-01D-1719-10 | g.chr3:114058003delG | c.2075delC | c.(2074-2076)cctfs | p.P692fs |
COADREAD | 3 | 114058003 | 114058003 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-CK-5913-01A-11D-1650-10 | TCGA-CK-5913-10A-01D-1650-10 | g.chr3:114058003delG | c.2075delC | c.(2074-2076)cctfs | p.P692fs |
COADREAD | 3 | 114058003 | 114058003 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-CK-5916-01A-11D-1650-10 | TCGA-CK-5916-10A-01D-1650-10 | g.chr3:114058003delG | c.2075delC | c.(2074-2076)cctfs | p.P692fs |
COADREAD | 3 | 114058003 | 114058003 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-CM-6171-01A-11D-1650-10 | TCGA-CM-6171-10A-01D-1650-10 | g.chr3:114058003delG | c.2075delC | c.(2074-2076)cctfs | p.P692fs |
COADREAD | 3 | 114058003 | 114058003 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-F4-6570-01A-11D-1771-10 | TCGA-F4-6570-10A-01D-1771-10 | g.chr3:114058003delG | c.2075delC | c.(2074-2076)cctfs | p.P692fs |
COADREAD | 3 | 114058003 | 114058003 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-F4-6856-01A-11D-1924-10 | TCGA-F4-6856-10A-01D-1924-10 | g.chr3:114058003delG | c.2075delC | c.(2074-2076)cctfs | p.P692fs |
COADREAD | 3 | 114058003 | 114058003 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr3:114058003delG | c.2075delC | c.(2074-2076)cctfs | p.P692fs |
COADREAD | 3 | 114058003 | 114058004 | + | Frame_Shift_Del | DEL | GG | GG | - | TCGA-A6-6780-01A-11D-1835-10 | TCGA-A6-6780-10A-01D-1835-10 | g.chr3:114058003_114058004delGG | c.2074_2075delCC | c.(2074-2076)cctfs | p.P692fs |
COADREAD | 3 | 114058003 | 114058004 | + | Frame_Shift_Del | DEL | GG | GG | - | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr3:114058003_114058004delGG | c.2074_2075delCC | c.(2074-2076)cctfs | p.P692fs |
COADREAD | 3 | 114058037 | 114058037 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3966-01A-01W-1073-09 | TCGA-AA-3966-10A-01W-1073-09 | g.chr3:114058037C>T | c.2041G>A | c.(2041-2043)Gtg>Atg | p.V681M |
COADREAD | 3 | 114058138 | 114058138 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3845-01A-01W-0995-10 | TCGA-AA-3845-10A-01W-0995-10 | g.chr3:114058138C>A | c.1940G>T | c.(1939-1941)aGc>aTc | p.S647I |
COADREAD | 3 | 114069325 | 114069325 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-6922-01A-11D-1924-10 | TCGA-D5-6922-10A-01D-1924-10 | g.chr3:114069325C>T | c.1600G>A | c.(1600-1602)Ggc>Agc | p.G534S |
COADREAD | 3 | 114069416 | 114069416 | + | Silent | SNP | A | A | G | TCGA-D5-6923-01A-11D-1924-10 | TCGA-D5-6923-10A-01D-1924-10 | g.chr3:114069416A>G | c.1509T>C | c.(1507-1509)gcT>gcC | p.A503A |
COADREAD | 3 | 114069732 | 114069732 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3815-01A-01W-0995-10 | TCGA-AA-3815-10A-01W-0995-10 | g.chr3:114069732G>A | c.1193C>T | c.(1192-1194)gCg>gTg | p.A398V |
COADREAD | 3 | 114069890 | 114069890 | + | Silent | SNP | C | C | T | TCGA-CM-6170-01A-11D-1650-10 | TCGA-CM-6170-10A-01D-1650-10 | g.chr3:114069890C>T | c.1035G>A | c.(1033-1035)gtG>gtA | p.V345V |
COADREAD | 3 | 114069891 | 114069891 | + | Missense_Mutation | SNP | A | A | G | TCGA-D5-6538-01A-11D-1719-10 | TCGA-D5-6538-10A-01D-1719-10 | g.chr3:114069891A>G | c.1034T>C | c.(1033-1035)gTg>gCg | p.V345A |
COADREAD | 3 | 114069901 | 114069901 | + | Missense_Mutation | SNP | G | G | T | TCGA-CK-6746-01A-11D-1835-10 | TCGA-CK-6746-10A-01D-1835-10 | g.chr3:114069901G>T | c.1024C>A | c.(1024-1026)Cag>Aag | p.Q342K |
COADREAD | 3 | 114069920 | 114069920 | + | Silent | SNP | G | G | A | TCGA-AG-A02N-01A-11W-A096-10 | TCGA-AG-A02N-11A-11W-A096-10 | g.chr3:114069920G>A | c.1005C>T | c.(1003-1005)gaC>gaT | p.D335D |
COADREAD | 3 | 114069920 | 114069920 | + | Silent | SNP | G | G | A | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chr3:114069920G>A | c.1005C>T | c.(1003-1005)gaC>gaT | p.D335D |
COADREAD | 3 | 114070037 | 114070037 | + | Silent | SNP | C | C | T | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr3:114070037C>T | c.888G>A | c.(886-888)caG>caA | p.Q296Q |
COADREAD | 3 | 114070275 | 114070275 | + | Missense_Mutation | SNP | T | T | C | TCGA-AD-6964-01A-11D-1924-10 | TCGA-AD-6964-10A-01D-1924-10 | g.chr3:114070275T>C | c.650A>G | c.(649-651)gAg>gGg | p.E217G |
COADREAD | 3 | 114070331 | 114070331 | + | Silent | SNP | G | G | A | TCGA-AA-3947-01A-01W-0995-10 | TCGA-AA-3947-10A-01W-0995-10 | g.chr3:114070331G>A | c.594C>T | c.(592-594)ggC>ggT | p.G198G |
COADREAD | 3 | 114070445 | 114070445 | + | Silent | SNP | G | G | A | TCGA-AA-A022-01A-21W-A096-10 | TCGA-AA-A022-11A-11W-A096-10 | g.chr3:114070445G>A | c.480C>T | c.(478-480)agC>agT | p.S160S |
COADREAD | 3 | 114070511 | 114070511 | + | Silent | SNP | G | G | A | TCGA-AZ-6601-01A-11D-1771-10 | TCGA-AZ-6601-11A-01D-1771-10 | g.chr3:114070511G>A | c.414C>T | c.(412-414)agC>agT | p.S138S |
COADREAD | 3 | 114070651 | 114070651 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-3892-01A-01W-1073-09 | TCGA-AG-3892-10A-01W-1073-09 | g.chr3:114070651C>T | c.274G>A | c.(274-276)Gag>Aag | p.E92K |
COADREAD | 3 | 114070695 | 114070695 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr3:114070695C>T | c.230G>A | c.(229-231)cGc>cAc | p.R77H |
DLBC | 3 | 114058008 | 114058008 | + | Silent | SNP | G | G | T | TCGA-GR-7351-01A-11D-2210-10 | TCGA-GR-7351-10A-01D-2210-10 | g.chr3:114058008G>T | c.2070C>A | c.(2068-2070)acC>acA | p.T690T |
DLBC | 3 | 114069130 | 114069130 | + | Missense_Mutation | SNP | C | C | T | TCGA-FF-8042-01A-11D-2210-10 | TCGA-FF-8042-10A-01D-2210-10 | g.chr3:114069130C>T | c.1795G>A | c.(1795-1797)Gta>Ata | p.V599I |
DLBC | 3 | 114070301 | 114070301 | + | Silent | SNP | G | G | C | TCGA-FA-A7Q1-01A-11D-A382-10 | TCGA-FA-A7Q1-10A-01D-A385-10 | g.chr3:114070301G>C | c.624C>G | c.(622-624)ggC>ggG | p.G208G |
ESCA | 3 | 114057910 | 114057910 | + | Missense_Mutation | SNP | T | T | G | TCGA-2H-A9GI-01A-11D-A37C-09 | TCGA-2H-A9GI-11A-11D-A37F-09 | g.chr3:114057910T>G | c.2168A>C | c.(2167-2169)aAg>aCg | p.K723T |
ESCA | 3 | 114058003 | 114058003 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-L5-A4OI-01A-11D-A27G-09 | TCGA-L5-A4OI-11A-11D-A27G-09 | g.chr3:114058003delG | c.2075delC | c.(2074-2076)cctfs | p.P692fs |
ESCA | 3 | 114069573 | 114069573 | + | Missense_Mutation | SNP | C | C | T | TCGA-L5-A8NR-01A-11D-A37C-09 | TCGA-L5-A8NR-11A-11D-A37F-09 | g.chr3:114069573C>T | c.1352G>A | c.(1351-1353)aGc>aAc | p.S451N |
ESCA | 3 | 114069876 | 114069876 | + | Missense_Mutation | SNP | C | C | T | TCGA-L5-A8NM-01A-11D-A37C-09 | TCGA-L5-A8NM-11A-12D-A37F-09 | g.chr3:114069876C>T | c.1049G>A | c.(1048-1050)cGc>cAc | p.R350H |
ESCA | 3 | 114070249 | 114070249 | + | Missense_Mutation | SNP | C | C | T | TCGA-VR-A8ET-01A-11D-A403-09 | TCGA-VR-A8ET-10B-01D-A403-09 | g.chr3:114070249C>T | c.676G>A | c.(676-678)Gac>Aac | p.D226N |
ESCA | 3 | 114070354 | 114070354 | + | Missense_Mutation | SNP | G | G | A | TCGA-L5-A4OI-01A-11D-A27G-09 | TCGA-L5-A4OI-11A-11D-A27G-09 | g.chr3:114070354G>A | c.571C>T | c.(571-573)Cgc>Tgc | p.R191C |
ESCA | 3 | 114099155 | 114099155 | + | Silent | SNP | C | C | T | TCGA-L5-A4OM-01A-11D-A27G-09 | TCGA-L5-A4OM-11A-11D-A27G-09 | g.chr3:114099155C>T | c.108G>A | c.(106-108)ctG>ctA | p.L36L |
GBM | 3 | 114069362 | 114069362 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-06-0132-01A-02D-1491-08 | TCGA-06-0132-10A-01D-1491-08 | g.chr3:114069362delG | c.1563delC | c.(1561-1563)cccfs | p.P521fs |
GBMLGG | 3 | 114057857 | 114057857 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6408-01A-11D-1705-08 | TCGA-DU-6408-10A-01D-1705-08 | g.chr3:114057857C>T | c.2221G>A | c.(2221-2223)Gga>Aga | p.G741R |
GBMLGG | 3 | 114058003 | 114058003 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-HT-8564-01A-11D-2395-08 | TCGA-HT-8564-10A-01D-2396-08 | g.chr3:114058003delG | c.2075delC | c.(2074-2076)cctfs | p.P692fs |
GBMLGG | 3 | 114058118 | 114058118 | + | Missense_Mutation | SNP | G | G | A | TCGA-DH-A7US-01A-11D-A33T-08 | TCGA-DH-A7US-10A-01D-A33W-08 | g.chr3:114058118G>A | c.1960C>T | c.(1960-1962)Cgc>Tgc | p.R654C |
GBMLGG | 3 | 114058129 | 114058129 | + | Missense_Mutation | SNP | T | T | C | TCGA-DB-A4XH-01A-11D-A27K-08 | TCGA-DB-A4XH-10A-01D-A27N-08 | g.chr3:114058129T>C | c.1949A>G | c.(1948-1950)aAc>aGc | p.N650S |
GBMLGG | 3 | 114058129 | 114058129 | + | Missense_Mutation | SNP | T | T | C | TCGA-DB-A64W-01A-11D-A29Q-08 | TCGA-DB-A64W-10A-01D-A29Q-08 | g.chr3:114058129T>C | c.1949A>G | c.(1948-1950)aAc>aGc | p.N650S |
GBMLGG | 3 | 114058129 | 114058129 | + | Missense_Mutation | SNP | T | T | C | TCGA-FG-8187-01A-11D-2253-08 | TCGA-FG-8187-10A-01D-2253-08 | g.chr3:114058129T>C | c.1949A>G | c.(1948-1950)aAc>aGc | p.N650S |
GBMLGG | 3 | 114058161 | 114058161 | + | Silent | SNP | G | G | A | TCGA-S9-A7QX-01A-11D-A34A-08 | TCGA-S9-A7QX-10A-01D-A34A-08 | g.chr3:114058161G>A | c.1917C>T | c.(1915-1917)tgC>tgT | p.C639C |
GBMLGG | 3 | 114058171 | 114058171 | + | Missense_Mutation | SNP | C | C | T | TCGA-RY-A847-01A-11D-A36O-08 | TCGA-RY-A847-10A-01D-A367-08 | g.chr3:114058171C>T | c.1907G>A | c.(1906-1908)tGt>tAt | p.C636Y |
GBMLGG | 3 | 114058203 | 114058203 | + | Missense_Mutation | SNP | C | C | G | TCGA-DB-A64V-01A-11D-A29Q-08 | TCGA-DB-A64V-10A-01D-A29Q-08 | g.chr3:114058203C>G | c.1875G>C | c.(1873-1875)atG>atC | p.M625I |
GBMLGG | 3 | 114058211 | 114058211 | + | Missense_Mutation | SNP | T | T | G | TCGA-HT-7608-01A-11D-2086-08 | TCGA-HT-7608-10A-01D-2086-08 | g.chr3:114058211T>G | c.1867A>C | c.(1867-1869)Aag>Cag | p.K623Q |
GBMLGG | 3 | 114058216 | 114058216 | + | Missense_Mutation | SNP | A | A | T | TCGA-QH-A65R-01A-21D-A31L-08 | TCGA-QH-A65R-10A-01D-A31J-08 | g.chr3:114058216A>T | c.1862T>A | c.(1861-1863)cTt>cAt | p.L621H |
GBMLGG | 3 | 114058228 | 114058230 | + | In_Frame_Del | DEL | AAG | AAG | - | TCGA-S9-A6WL-01A-21D-A33T-08 | TCGA-S9-A6WL-10A-01D-A33W-08 | g.chr3:114058228_114058230delAAG | c.1848_1850delCTT | c.(1846-1851)tcctta>tca | p.L617del |
GBMLGG | 3 | 114058229 | 114058231 | + | In_Frame_Del | DEL | AGG | AGG | - | TCGA-HW-A5KJ-01A-12D-A27K-08 | TCGA-HW-A5KJ-10A-01D-A27N-08 | g.chr3:114058229_114058231delAGG | c.1847_1849delCCT | c.(1846-1851)tcctta>tta | p.S616del |
GBMLGG | 3 | 114058232 | 114058234 | + | In_Frame_Del | DEL | AGA | AGA | - | TCGA-P5-A5ET-01A-11D-A27K-08 | TCGA-P5-A5ET-10A-01D-A27N-08 | g.chr3:114058232_114058234delAGA | c.1844_1846delTCT | c.(1843-1848)ttctcc>tcc | p.F615del |
GBMLGG | 3 | 114058240 | 114058240 | + | Missense_Mutation | SNP | C | C | T | TCGA-E1-A7YS-01A-11D-A34A-08 | TCGA-E1-A7YS-10A-01D-A34A-08 | g.chr3:114058240C>T | c.1838G>A | c.(1837-1839)cGc>cAc | p.R613H |
GBMLGG | 3 | 114069124 | 114069124 | + | Missense_Mutation | SNP | T | T | C | TCGA-FG-A6J1-01A-11D-A31L-08 | TCGA-FG-A6J1-10A-01D-A31J-08 | g.chr3:114069124T>C | c.1801A>G | c.(1801-1803)Aca>Gca | p.T601A |
GBMLGG | 3 | 114069165 | 114069166 | + | Frame_Shift_Del | DEL | AA | AA | - | TCGA-HT-7605-01A-11D-2086-08 | TCGA-HT-7605-10A-01D-2086-08 | g.chr3:114069165_114069166delAA | c.1759_1760delTT | c.(1759-1761)ttcfs | p.F587fs |
GBMLGG | 3 | 114069362 | 114069362 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-06-0132-01A-02D-1491-08 | TCGA-06-0132-10A-01D-1491-08 | g.chr3:114069362delG | c.1563delC | c.(1561-1563)cccfs | p.P521fs |
GBMLGG | 3 | 114069362 | 114069362 | + | Silent | SNP | G | G | A | TCGA-DU-6393-01A-11D-1705-08 | TCGA-DU-6393-10A-01D-1705-08 | g.chr3:114069362G>A | c.1563C>T | c.(1561-1563)ccC>ccT | p.P521P |
GBMLGG | 3 | 114070191 | 114070191 | + | Missense_Mutation | SNP | G | G | A | TCGA-DH-A7US-01A-11D-A33T-08 | TCGA-DH-A7US-10A-01D-A33W-08 | g.chr3:114070191G>A | c.734C>T | c.(733-735)tCg>tTg | p.S245L |
GBMLGG | 3 | 114070191 | 114070191 | + | Missense_Mutation | SNP | G | G | C | TCGA-HT-7881-01A-11D-2395-08 | TCGA-HT-7881-10A-01D-2396-08 | g.chr3:114070191G>C | c.734C>G | c.(733-735)tCg>tGg | p.S245W |
GBMLGG | 3 | 114070194 | 114070194 | + | Missense_Mutation | SNP | T | T | C | TCGA-DU-5849-01A-11D-1705-08 | TCGA-DU-5849-10A-01D-1705-08 | g.chr3:114070194T>C | c.731A>G | c.(730-732)tAc>tGc | p.Y244C |
GBMLGG | 3 | 114070216 | 114070216 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-HT-8563-01A-11D-2395-08 | TCGA-HT-8563-10A-01D-2396-08 | g.chr3:114070216G>A | c.709C>T | c.(709-711)Cag>Tag | p.Q237* |
GBMLGG | 3 | 114070289 | 114070289 | + | Silent | SNP | C | C | T | TCGA-FG-A60K-01A-11D-A29Q-08 | TCGA-FG-A60K-10A-01D-A29Q-08 | g.chr3:114070289C>T | c.636G>A | c.(634-636)ccG>ccA | p.P212P |
GBMLGG | 3 | 114070389 | 114070389 | + | Missense_Mutation | SNP | A | A | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr3:114070389A>G | c.536T>C | c.(535-537)aTc>aCc | p.I179T |
GBMLGG | 3 | 114070470 | 114070478 | + | In_Frame_Del | DEL | TGCACTGAC | TGCACTGAC | - | TCGA-TQ-A7RV-01A-21D-A34A-08 | TCGA-TQ-A7RV-10A-01D-A34A-08 | g.chr3:114070470_114070478delTGCACTGAC | c.447_455delGTCAGTGCA | c.(445-456)cagtcagtgcaa>caa | p.149_152QSVQ>Q |
HNSC | 3 | 114057937 | 114057937 | + | Missense_Mutation | SNP | G | G | C | TCGA-CN-4726-01A-01D-1434-08 | TCGA-CN-4726-10A-01D-1434-08 | g.chr3:114057937G>C | c.2141C>G | c.(2140-2142)aCt>aGt | p.T714S |
HNSC | 3 | 114058003 | 114058003 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr3:114058003delG | c.2075delC | c.(2074-2076)cctfs | p.P692fs |
HNSC | 3 | 114058003 | 114058003 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-QK-A6VB-01A-12D-A34J-08 | TCGA-QK-A6VB-10B-01D-A34M-08 | g.chr3:114058003delG | c.2075delC | c.(2074-2076)cctfs | p.P692fs |
HNSC | 3 | 114058212 | 114058212 | + | Silent | SNP | G | G | T | TCGA-CV-A461-01A-41D-A25Y-08 | TCGA-CV-A461-10A-01D-A25Y-08 | g.chr3:114058212G>T | c.1866C>A | c.(1864-1866)atC>atA | p.I622I |
HNSC | 3 | 114069347 | 114069347 | + | Silent | SNP | G | G | A | TCGA-BA-4077-01B-01D-1434-08 | TCGA-BA-4077-10A-01D-1434-08 | g.chr3:114069347G>A | c.1578C>T | c.(1576-1578)ttC>ttT | p.F526F |
HNSC | 3 | 114069375 | 114069375 | + | Missense_Mutation | SNP | G | G | A | TCGA-CN-6992-01A-11D-1912-08 | TCGA-CN-6992-10A-01D-1912-08 | g.chr3:114069375G>A | c.1550C>T | c.(1549-1551)gCg>gTg | p.A517V |
HNSC | 3 | 114069466 | 114069466 | + | Missense_Mutation | SNP | G | G | C | TCGA-CV-A6JN-01A-11D-A31L-08 | TCGA-CV-A6JN-10A-01D-A31J-08 | g.chr3:114069466G>C | c.1459C>G | c.(1459-1461)Ctg>Gtg | p.L487V |
HNSC | 3 | 114069659 | 114069659 | + | Missense_Mutation | SNP | C | C | A | TCGA-D6-A6EK-01A-11D-A31L-08 | TCGA-D6-A6EK-10A-01D-A31J-08 | g.chr3:114069659C>A | c.1266G>T | c.(1264-1266)caG>caT | p.Q422H |
HNSC | 3 | 114069727 | 114069727 | + | Silent | SNP | G | G | T | TCGA-CV-5441-01A-01D-1512-08 | TCGA-CV-5441-11A-01D-1512-08 | g.chr3:114069727G>T | c.1198C>A | c.(1198-1200)Cgg>Agg | p.R400R |
HNSC | 3 | 114070078 | 114070078 | + | Missense_Mutation | SNP | C | C | T | TCGA-BA-4077-01B-01D-1434-08 | TCGA-BA-4077-10A-01D-1434-08 | g.chr3:114070078C>T | c.847G>A | c.(847-849)Gaa>Aaa | p.E283K |
HNSC | 3 | 114070150 | 114070150 | + | Missense_Mutation | SNP | G | G | A | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr3:114070150G>A | c.775C>T | c.(775-777)Cgc>Tgc | p.R259C |
HNSC | 3 | 114070207 | 114070207 | + | Missense_Mutation | SNP | C | C | T | TCGA-P3-A6SW-01A-11D-A34J-08 | TCGA-P3-A6SW-10A-01D-A34M-08 | g.chr3:114070207C>T | c.718G>A | c.(718-720)Gtg>Atg | p.V240M |
HNSC | 3 | 114070460 | 114070460 | + | Silent | SNP | A | A | T | TCGA-CN-A6V1-01A-12D-A34J-08 | TCGA-CN-A6V1-10B-01D-A34M-08 | g.chr3:114070460A>T | c.465T>A | c.(463-465)atT>atA | p.I155I |
KICH | 3 | 114070436 | 114070436 | + | Silent | SNP | T | T | C | TCGA-KN-8425-01A-11D-2310-10 | TCGA-KN-8425-11A-01D-2310-10 | g.chr3:114070436T>C | c.489A>G | c.(487-489)ctA>ctG | p.L163L |
KIPAN | 3 | 114057877 | 114057878 | + | Frame_Shift_Del | DEL | AT | AT | - | TCGA-GL-7773-01A-11D-2136-08 | TCGA-GL-7773-10A-01D-2136-08 | g.chr3:114057877_114057878delAT | c.2200_2201delAT | c.(2200-2202)atgfs | p.M734fs |
KIPAN | 3 | 114058081 | 114058081 | + | Missense_Mutation | SNP | A | A | G | TCGA-BP-5182-01A-01D-1429-08 | TCGA-BP-5182-11A-01D-1429-08 | g.chr3:114058081A>G | c.1997T>C | c.(1996-1998)aTc>aCc | p.I666T |
KIPAN | 3 | 114070318 | 114070318 | + | Missense_Mutation | SNP | C | C | T | TCGA-B0-5698-01A-11D-1669-08 | TCGA-B0-5698-10A-01D-1669-08 | g.chr3:114070318C>T | c.607G>A | c.(607-609)Ggg>Agg | p.G203R |
KIPAN | 3 | 114070436 | 114070436 | + | Silent | SNP | T | T | C | TCGA-KN-8425-01A-11D-2310-10 | TCGA-KN-8425-11A-01D-2310-10 | g.chr3:114070436T>C | c.489A>G | c.(487-489)ctA>ctG | p.L163L |
KIRC | 3 | 114058081 | 114058081 | + | Missense_Mutation | SNP | A | A | G | TCGA-BP-5182-01A-01D-1429-08 | TCGA-BP-5182-11A-01D-1429-08 | g.chr3:114058081A>G | c.1997T>C | c.(1996-1998)aTc>aCc | p.I666T |
KIRC | 3 | 114070318 | 114070318 | + | Missense_Mutation | SNP | C | C | T | TCGA-B0-5698-01A-11D-1669-08 | TCGA-B0-5698-10A-01D-1669-08 | g.chr3:114070318C>T | c.607G>A | c.(607-609)Ggg>Agg | p.G203R |
KIRP | 3 | 114057877 | 114057878 | + | Frame_Shift_Del | DEL | AT | AT | - | TCGA-GL-7773-01A-11D-2136-08 | TCGA-GL-7773-10A-01D-2136-08 | g.chr3:114057877_114057878delAT | c.2200_2201delAT | c.(2200-2202)atgfs | p.M734fs |
LGG | 3 | 114057857 | 114057857 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6408-01A-11D-1705-08 | TCGA-DU-6408-10A-01D-1705-08 | g.chr3:114057857C>T | c.2221G>A | c.(2221-2223)Gga>Aga | p.G741R |
LGG | 3 | 114058003 | 114058003 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-HT-8564-01A-11D-2395-08 | TCGA-HT-8564-10A-01D-2396-08 | g.chr3:114058003delG | c.2075delC | c.(2074-2076)cctfs | p.P692fs |
LGG | 3 | 114058118 | 114058118 | + | Missense_Mutation | SNP | G | G | A | TCGA-DH-A7US-01A-11D-A33T-08 | TCGA-DH-A7US-10A-01D-A33W-08 | g.chr3:114058118G>A | c.1960C>T | c.(1960-1962)Cgc>Tgc | p.R654C |
LGG | 3 | 114058129 | 114058129 | + | Missense_Mutation | SNP | T | T | C | TCGA-DB-A4XH-01A-11D-A27K-08 | TCGA-DB-A4XH-10A-01D-A27N-08 | g.chr3:114058129T>C | c.1949A>G | c.(1948-1950)aAc>aGc | p.N650S |
LGG | 3 | 114058129 | 114058129 | + | Missense_Mutation | SNP | T | T | C | TCGA-DB-A64W-01A-11D-A29Q-08 | TCGA-DB-A64W-10A-01D-A29Q-08 | g.chr3:114058129T>C | c.1949A>G | c.(1948-1950)aAc>aGc | p.N650S |
LGG | 3 | 114058129 | 114058129 | + | Missense_Mutation | SNP | T | T | C | TCGA-FG-8187-01A-11D-2253-08 | TCGA-FG-8187-10A-01D-2253-08 | g.chr3:114058129T>C | c.1949A>G | c.(1948-1950)aAc>aGc | p.N650S |
LGG | 3 | 114058161 | 114058161 | + | Silent | SNP | G | G | A | TCGA-S9-A7QX-01A-11D-A34A-08 | TCGA-S9-A7QX-10A-01D-A34A-08 | g.chr3:114058161G>A | c.1917C>T | c.(1915-1917)tgC>tgT | p.C639C |
LGG | 3 | 114058171 | 114058171 | + | Missense_Mutation | SNP | C | C | T | TCGA-RY-A847-01A-11D-A36O-08 | TCGA-RY-A847-10A-01D-A367-08 | g.chr3:114058171C>T | c.1907G>A | c.(1906-1908)tGt>tAt | p.C636Y |
LGG | 3 | 114058203 | 114058203 | + | Missense_Mutation | SNP | C | C | G | TCGA-DB-A64V-01A-11D-A29Q-08 | TCGA-DB-A64V-10A-01D-A29Q-08 | g.chr3:114058203C>G | c.1875G>C | c.(1873-1875)atG>atC | p.M625I |
LGG | 3 | 114058211 | 114058211 | + | Missense_Mutation | SNP | T | T | G | TCGA-HT-7608-01A-11D-2086-08 | TCGA-HT-7608-10A-01D-2086-08 | g.chr3:114058211T>G | c.1867A>C | c.(1867-1869)Aag>Cag | p.K623Q |
LGG | 3 | 114058216 | 114058216 | + | Missense_Mutation | SNP | A | A | T | TCGA-QH-A65R-01A-21D-A31L-08 | TCGA-QH-A65R-10A-01D-A31J-08 | g.chr3:114058216A>T | c.1862T>A | c.(1861-1863)cTt>cAt | p.L621H |
LGG | 3 | 114058228 | 114058230 | + | In_Frame_Del | DEL | AAG | AAG | - | TCGA-S9-A6WL-01A-21D-A33T-08 | TCGA-S9-A6WL-10A-01D-A33W-08 | g.chr3:114058228_114058230delAAG | c.1848_1850delCTT | c.(1846-1851)tcctta>tca | p.L617del |
LGG | 3 | 114058229 | 114058231 | + | In_Frame_Del | DEL | AGG | AGG | - | TCGA-HW-A5KJ-01A-12D-A27K-08 | TCGA-HW-A5KJ-10A-01D-A27N-08 | g.chr3:114058229_114058231delAGG | c.1847_1849delCCT | c.(1846-1851)tcctta>tta | p.S616del |
LGG | 3 | 114058232 | 114058234 | + | In_Frame_Del | DEL | AGA | AGA | - | TCGA-P5-A5ET-01A-11D-A27K-08 | TCGA-P5-A5ET-10A-01D-A27N-08 | g.chr3:114058232_114058234delAGA | c.1844_1846delTCT | c.(1843-1848)ttctcc>tcc | p.F615del |
LGG | 3 | 114058240 | 114058240 | + | Missense_Mutation | SNP | C | C | T | TCGA-E1-A7YS-01A-11D-A34A-08 | TCGA-E1-A7YS-10A-01D-A34A-08 | g.chr3:114058240C>T | c.1838G>A | c.(1837-1839)cGc>cAc | p.R613H |
LGG | 3 | 114069124 | 114069124 | + | Missense_Mutation | SNP | T | T | C | TCGA-FG-A6J1-01A-11D-A31L-08 | TCGA-FG-A6J1-10A-01D-A31J-08 | g.chr3:114069124T>C | c.1801A>G | c.(1801-1803)Aca>Gca | p.T601A |
LGG | 3 | 114069165 | 114069166 | + | Frame_Shift_Del | DEL | AA | AA | - | TCGA-HT-7605-01A-11D-2086-08 | TCGA-HT-7605-10A-01D-2086-08 | g.chr3:114069165_114069166delAA | c.1759_1760delTT | c.(1759-1761)ttcfs | p.F587fs |
LGG | 3 | 114069362 | 114069362 | + | Silent | SNP | G | G | A | TCGA-DU-6393-01A-11D-1705-08 | TCGA-DU-6393-10A-01D-1705-08 | g.chr3:114069362G>A | c.1563C>T | c.(1561-1563)ccC>ccT | p.P521P |
LGG | 3 | 114070191 | 114070191 | + | Missense_Mutation | SNP | G | G | A | TCGA-DH-A7US-01A-11D-A33T-08 | TCGA-DH-A7US-10A-01D-A33W-08 | g.chr3:114070191G>A | c.734C>T | c.(733-735)tCg>tTg | p.S245L |
LGG | 3 | 114070191 | 114070191 | + | Missense_Mutation | SNP | G | G | C | TCGA-HT-7881-01A-11D-2395-08 | TCGA-HT-7881-10A-01D-2396-08 | g.chr3:114070191G>C | c.734C>G | c.(733-735)tCg>tGg | p.S245W |
LGG | 3 | 114070194 | 114070194 | + | Missense_Mutation | SNP | T | T | C | TCGA-DU-5849-01A-11D-1705-08 | TCGA-DU-5849-10A-01D-1705-08 | g.chr3:114070194T>C | c.731A>G | c.(730-732)tAc>tGc | p.Y244C |
LGG | 3 | 114070216 | 114070216 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-HT-8563-01A-11D-2395-08 | TCGA-HT-8563-10A-01D-2396-08 | g.chr3:114070216G>A | c.709C>T | c.(709-711)Cag>Tag | p.Q237* |
LGG | 3 | 114070289 | 114070289 | + | Silent | SNP | C | C | T | TCGA-FG-A60K-01A-11D-A29Q-08 | TCGA-FG-A60K-10A-01D-A29Q-08 | g.chr3:114070289C>T | c.636G>A | c.(634-636)ccG>ccA | p.P212P |
LGG | 3 | 114070389 | 114070389 | + | Missense_Mutation | SNP | A | A | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr3:114070389A>G | c.536T>C | c.(535-537)aTc>aCc | p.I179T |
LGG | 3 | 114070470 | 114070478 | + | In_Frame_Del | DEL | TGCACTGAC | TGCACTGAC | - | TCGA-TQ-A7RV-01A-21D-A34A-08 | TCGA-TQ-A7RV-10A-01D-A34A-08 | g.chr3:114070470_114070478delTGCACTGAC | c.447_455delGTCAGTGCA | c.(445-456)cagtcagtgcaa>caa | p.149_152QSVQ>Q |
LIHC | 3 | 114058003 | 114058003 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-ED-A7PZ-01A-11D-A33Q-10 | TCGA-ED-A7PZ-10A-01D-A33Q-10 | g.chr3:114058003delG | c.2075delC | c.(2074-2076)cctfs | p.P692fs |
LIHC | 3 | 114070331 | 114070331 | + | Silent | SNP | G | G | A | TCGA-4R-AA8I-01A-11D-A382-10 | TCGA-4R-AA8I-10B-01D-A385-10 | g.chr3:114070331G>A | c.594C>T | c.(592-594)ggC>ggT | p.G198G |
LIHC | 3 | 114070355 | 114070355 | + | Silent | SNP | C | C | T | TCGA-KR-A7K7-01A-11D-A33K-10 | TCGA-KR-A7K7-10A-01D-A33K-10 | g.chr3:114070355C>T | c.570G>A | c.(568-570)acG>acA | p.T190T |
LUAD | 3 | 114057870 | 114057870 | + | Missense_Mutation | SNP | C | C | A | TCGA-55-1592-01A-01D-0969-08 | TCGA-55-1592-11A-01D-0969-08 | g.chr3:114057870C>A | c.2208G>T | c.(2206-2208)atG>atT | p.M736I |
LUAD | 3 | 114058003 | 114058003 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-86-A4JF-01A-11D-A24P-08 | TCGA-86-A4JF-10A-01D-A24P-08 | g.chr3:114058003delG | c.2075delC | c.(2074-2076)cctfs | p.P692fs |
LUAD | 3 | 114058243 | 114058243 | + | Missense_Mutation | SNP | C | C | A | TCGA-86-A4JF-01A-11D-A24P-08 | TCGA-86-A4JF-10A-01D-A24P-08 | g.chr3:114058243C>A | c.1835G>T | c.(1834-1836)tGg>tTg | p.W612L |
LUAD | 3 | 114069274 | 114069274 | + | Missense_Mutation | SNP | T | T | A | TCGA-55-6969-01A-11D-1945-08 | TCGA-55-6969-11A-01D-1945-08 | g.chr3:114069274T>A | c.1651A>T | c.(1651-1653)Act>Tct | p.T551S |
LUAD | 3 | 114069321 | 114069321 | + | Missense_Mutation | SNP | T | T | A | TCGA-50-5941-01A-11D-1753-08 | TCGA-50-5941-10A-01D-1753-08 | g.chr3:114069321T>A | c.1604A>T | c.(1603-1605)cAg>cTg | p.Q535L |
LUAD | 3 | 114069589 | 114069589 | + | Missense_Mutation | SNP | T | T | A | TCGA-17-Z044-01A-01W-0746-08 | TCGA-17-Z044-11A-01W-0746-08 | g.chr3:114069589T>A | c.1336A>T | c.(1336-1338)Atc>Ttc | p.I446F |
LUAD | 3 | 114069637 | 114069637 | + | Missense_Mutation | SNP | C | C | T | TCGA-55-8301-01A-11D-2284-08 | TCGA-55-8301-10A-01D-2284-08 | g.chr3:114069637C>T | c.1288G>A | c.(1288-1290)Gct>Act | p.A430T |
LUAD | 3 | 114069647 | 114069647 | + | Silent | SNP | T | T | C | TCGA-17-Z031-01A-01W-0746-08 | TCGA-17-Z031-11A-01W-0746-08 | g.chr3:114069647T>C | c.1278A>G | c.(1276-1278)ctA>ctG | p.L426L |
LUAD | 3 | 114069675 | 114069675 | + | Missense_Mutation | SNP | G | G | C | TCGA-62-A46S-01A-11D-A24D-08 | TCGA-62-A46S-10A-01D-A24F-08 | g.chr3:114069675G>C | c.1250C>G | c.(1249-1251)gCt>gGt | p.A417G |
LUAD | 3 | 114069770 | 114069770 | + | Silent | SNP | G | G | A | TCGA-44-3918-01A-01D-1105-08 | TCGA-44-3918-11A-01D-1105-08 | g.chr3:114069770G>A | c.1155C>T | c.(1153-1155)acC>acT | p.T385T |
LUAD | 3 | 114069779 | 114069779 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-97-8172-01A-11D-2284-08 | TCGA-97-8172-10A-01D-2284-08 | g.chr3:114069779delG | c.1146delC | c.(1144-1146)tccfs | p.S382fs |
LUAD | 3 | 114069802 | 114069802 | + | Missense_Mutation | SNP | A | A | C | TCGA-62-8399-01A-21D-2323-08 | TCGA-62-8399-10A-01D-2323-08 | g.chr3:114069802A>C | c.1123T>G | c.(1123-1125)Ttc>Gtc | p.F375V |
LUAD | 3 | 114070030 | 114070030 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-78-7220-01A-11D-2036-08 | TCGA-78-7220-10A-01D-2036-08 | g.chr3:114070030C>A | c.895G>T | c.(895-897)Gag>Tag | p.E299* |
LUAD | 3 | 114070047 | 114070047 | + | Missense_Mutation | SNP | T | T | G | TCGA-78-7155-01A-11D-2036-08 | TCGA-78-7155-10A-01D-2036-08 | g.chr3:114070047T>G | c.878A>C | c.(877-879)gAg>gCg | p.E293A |
LUAD | 3 | 114070127 | 114070127 | + | Silent | SNP | C | C | A | TCGA-97-8172-01A-11D-2284-08 | TCGA-97-8172-10A-01D-2284-08 | g.chr3:114070127C>A | c.798G>T | c.(796-798)gtG>gtT | p.V266V |
LUAD | 3 | 114070151 | 114070151 | + | Missense_Mutation | SNP | C | C | G | TCGA-17-Z050-01A-01W-0747-08 | TCGA-17-Z050-11A-01W-0747-08 | g.chr3:114070151C>G | c.774G>C | c.(772-774)gaG>gaC | p.E258D |
LUAD | 3 | 114070211 | 114070211 | + | Missense_Mutation | SNP | G | G | C | TCGA-17-Z047-01A-01W-0747-08 | TCGA-17-Z047-11A-01W-0746-08 | g.chr3:114070211G>C | c.714C>G | c.(712-714)caC>caG | p.H238Q |
LUAD | 3 | 114070243 | 114070243 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-97-7547-01A-11D-2036-08 | TCGA-97-7547-10A-01D-2036-08 | g.chr3:114070243C>A | c.682G>T | c.(682-684)Gag>Tag | p.E228* |
LUAD | 3 | 114070281 | 114070281 | + | Missense_Mutation | SNP | G | G | C | TCGA-86-7955-01A-11D-2184-08 | TCGA-86-7955-10A-01D-2184-08 | g.chr3:114070281G>C | c.644C>G | c.(643-645)aCt>aGt | p.T215S |
LUAD | 3 | 114070473 | 114070473 | + | Missense_Mutation | SNP | A | A | C | TCGA-05-4432-01A-01D-1265-08 | TCGA-05-4432-10A-01D-1265-08 | g.chr3:114070473A>C | c.452T>G | c.(451-453)gTg>gGg | p.V151G |
LUAD | 3 | 114070511 | 114070511 | + | Silent | SNP | G | G | A | TCGA-67-4679-01B-01D-1753-08 | TCGA-67-4679-10A-01D-1753-08 | g.chr3:114070511G>A | c.414C>T | c.(412-414)agC>agT | p.S138S |
LUAD | 3 | 114070610 | 114070610 | + | Missense_Mutation | SNP | G | G | C | TCGA-55-6969-01A-11D-1945-08 | TCGA-55-6969-11A-01D-1945-08 | g.chr3:114070610G>C | c.315C>G | c.(313-315)gaC>gaG | p.D105E |
LUAD | 3 | 114070631 | 114070631 | + | Silent | SNP | G | G | A | TCGA-86-8281-01A-11D-2284-08 | TCGA-86-8281-10A-01D-2284-08 | g.chr3:114070631G>A | c.294C>T | c.(292-294)cgC>cgT | p.R98R |
LUSC | 3 | 114058223 | 114058223 | + | Missense_Mutation | SNP | C | C | G | TCGA-18-3417-01A-01D-1441-08 | TCGA-18-3417-11A-01D-1441-08 | g.chr3:114058223C>G | c.1855G>C | c.(1855-1857)Gat>Cat | p.D619H |
LUSC | 3 | 114069245 | 114069245 | + | Silent | SNP | C | C | A | TCGA-37-5819-01A-01D-1632-08 | TCGA-37-5819-10A-01D-1632-08 | g.chr3:114069245C>A | c.1680G>T | c.(1678-1680)ctG>ctT | p.L560L |
LUSC | 3 | 114069570 | 114069570 | + | Missense_Mutation | SNP | G | G | A | TCGA-18-3409-01A-01D-0983-08 | TCGA-18-3409-11A-01D-0983-08 | g.chr3:114069570G>A | c.1355C>T | c.(1354-1356)tCc>tTc | p.S452F |
LUSC | 3 | 114069951 | 114069951 | + | Missense_Mutation | SNP | C | C | G | TCGA-85-6560-01A-11D-1817-08 | TCGA-85-6560-10A-01D-1817-08 | g.chr3:114069951C>G | c.974G>C | c.(973-975)gGc>gCc | p.G325A |
LUSC | 3 | 114070037 | 114070037 | + | Silent | SNP | C | C | T | TCGA-37-4133-01A-01D-1352-08 | TCGA-37-4133-10A-01D-1352-08 | g.chr3:114070037C>T | c.888G>A | c.(886-888)caG>caA | p.Q296Q |
LUSC | 3 | 114070156 | 114070156 | + | Missense_Mutation | SNP | C | C | T | TCGA-22-5489-01A-01D-1632-08 | TCGA-22-5489-11A-01D-1632-08 | g.chr3:114070156C>T | c.769G>A | c.(769-771)Ggc>Agc | p.G257S |
LUSC | 3 | 114070355 | 114070355 | + | Silent | SNP | C | C | T | TCGA-34-5927-01A-11D-1817-08 | TCGA-34-5927-10A-01D-1817-08 | g.chr3:114070355C>T | c.570G>A | c.(568-570)acG>acA | p.T190T |
LUSC | 3 | 114070442 | 114070442 | + | Silent | SNP | G | G | A | TCGA-18-5595-01A-01D-1632-08 | TCGA-18-5595-11A-01D-1632-08 | g.chr3:114070442G>A | c.483C>T | c.(481-483)ggC>ggT | p.G161G |
LUSC | 3 | 114070443 | 114070443 | + | Missense_Mutation | SNP | C | C | A | TCGA-70-6722-01A-11D-1817-08 | TCGA-70-6722-10A-01D-1817-08 | g.chr3:114070443C>A | c.482G>T | c.(481-483)gGc>gTc | p.G161V |
OV | 3 | 114057992 | 114057992 | + | Missense_Mutation | SNP | G | G | T | TCGA-23-1022-01A-02W-0488-09 | TCGA-23-1022-10A-01W-0488-09 | g.chr3:114057992G>T | c.2086C>A | c.(2086-2088)Ccc>Acc | p.P696T |
OV | 3 | 114069418 | 114069418 | + | Missense_Mutation | SNP | C | C | A | TCGA-04-1343-01A-01W-0488-09 | TCGA-04-1343-10A-01W-0489-09 | g.chr3:114069418C>A | c.1507G>T | c.(1507-1509)Gct>Tct | p.A503S |
OV | 3 | 114069698 | 114069698 | + | Silent | SNP | G | G | A | TCGA-29-1710-01A-02W-0633-09 | TCGA-29-1710-10A-01W-0633-09 | g.chr3:114069698G>A | c.1227C>T | c.(1225-1227)ccC>ccT | p.P409P |
OV | 3 | 114069892 | 114069892 | + | Missense_Mutation | SNP | C | C | G | TCGA-13-0923-01A-01W-0420-08 | TCGA-13-0923-10A-01D-0399-08 | g.chr3:114069892C>G | c.1033G>C | c.(1033-1035)Gtg>Ctg | p.V345L |
OV | 3 | 114070129 | 114070129 | + | Missense_Mutation | SNP | C | C | T | TCGA-23-2072-01A-01W-0722-08 | TCGA-23-2072-10A-01W-0722-08 | g.chr3:114070129C>T | c.796G>A | c.(796-798)Gtg>Atg | p.V266M |
PAAD | 3 | 114058034 | 114058034 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr3:114058034C>T | c.2044G>A | c.(2044-2046)Gcc>Acc | p.A682T |
PAAD | 3 | 114069198 | 114069198 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-IB-A6UF-01A-23D-A33T-08 | TCGA-IB-A6UF-10A-01D-A33W-08 | g.chr3:114069198delT | c.1727delA | c.(1726-1728)aagfs | p.K576fs |
PAAD | 3 | 114069698 | 114069698 | + | Silent | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr3:114069698G>A | c.1227C>T | c.(1225-1227)ccC>ccT | p.P409P |
PAAD | 3 | 114069836 | 114069836 | + | Silent | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr3:114069836G>A | c.1089C>T | c.(1087-1089)gcC>gcT | p.A363A |
PAAD | 3 | 114070337 | 114070337 | + | Silent | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr3:114070337G>A | c.588C>T | c.(586-588)aaC>aaT | p.N196N |
PAAD | 3 | 114070553 | 114070553 | + | Silent | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr3:114070553G>A | c.372C>T | c.(370-372)gcC>gcT | p.A124A |
PAAD | 3 | 114070605 | 114070605 | + | Missense_Mutation | SNP | G | G | A | TCGA-IB-AAUR-01A-21D-A38G-08 | TCGA-IB-AAUR-10A-01D-A38J-08 | g.chr3:114070605G>A | c.320C>T | c.(319-321)aCg>aTg | p.T107M |
PAAD | 3 | 114070695 | 114070695 | + | Missense_Mutation | SNP | C | C | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr3:114070695C>T | c.230G>A | c.(229-231)cGc>cAc | p.R77H |
PRAD | 3 | 114058118 | 114058118 | + | Missense_Mutation | SNP | G | G | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr3:114058118G>A | c.1960C>T | c.(1960-1962)Cgc>Tgc | p.R654C |
PRAD | 3 | 114069597 | 114069597 | + | Missense_Mutation | SNP | C | C | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr3:114069597C>A | c.1328G>T | c.(1327-1329)aGc>aTc | p.S443I |
PRAD | 3 | 114069639 | 114069639 | + | Missense_Mutation | SNP | C | C | A | TCGA-VN-A88P-01A-11D-A34U-08 | TCGA-VN-A88P-10A-01D-A34X-08 | g.chr3:114069639C>A | c.1286G>T | c.(1285-1287)gGt>gTt | p.G429V |
READ | 3 | 114069920 | 114069920 | + | Silent | SNP | G | G | A | TCGA-AG-A02N-01A-11W-A096-10 | TCGA-AG-A02N-11A-11W-A096-10 | g.chr3:114069920G>A | c.1005C>T | c.(1003-1005)gaC>gaT | p.D335D |
READ | 3 | 114070651 | 114070651 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-3892-01A-01W-1073-09 | TCGA-AG-3892-10A-01W-1073-09 | g.chr3:114070651C>T | c.274G>A | c.(274-276)Gag>Aag | p.E92K |
READ | 3 | 114070695 | 114070695 | + | Missense_Mutation | SNP | C | C | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr3:114070695C>T | c.230G>A | c.(229-231)cGc>cAc | p.R77H |
SARC | 3 | 114057869 | 114057869 | + | Missense_Mutation | SNP | G | G | A | TCGA-Z4-AAPG-01A-11D-A38Z-09 | TCGA-Z4-AAPG-10A-01D-A38Z-09 | g.chr3:114057869G>A | c.2209C>T | c.(2209-2211)Cat>Tat | p.H737Y |
SARC | 3 | 114069530 | 114069530 | + | Silent | SNP | G | G | A | TCGA-QC-A7B5-01A-11D-A33E-09 | TCGA-QC-A7B5-11A-11D-A33H-09 | g.chr3:114069530G>A | c.1395C>T | c.(1393-1395)tcC>tcT | p.S465S |
SKCM | 3 | 114057948 | 114057948 | + | Silent | SNP | C | C | T | TCGA-D3-A3C3-06A-12D-A19A-08 | TCGA-D3-A3C3-10A-01D-A19A-08 | g.chr3:114057948C>T | c.2130G>A | c.(2128-2130)acG>acA | p.T710T |
SKCM | 3 | 114057955 | 114057955 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr3:114057955G>A | c.2123C>T | c.(2122-2124)gCc>gTc | p.A708V |
SKCM | 3 | 114058095 | 114058095 | + | Silent | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr3:114058095G>A | c.1983C>T | c.(1981-1983)tcC>tcT | p.S661S |
SKCM | 3 | 114058118 | 114058118 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A1Q3-06A-11D-A196-08 | TCGA-D3-A1Q3-10A-01D-A198-08 | g.chr3:114058118G>A | c.1960C>T | c.(1960-1962)Cgc>Tgc | p.R654C |
SKCM | 3 | 114069131 | 114069131 | + | Silent | SNP | G | G | A | TCGA-D3-A51G-06A-11D-A25O-08 | TCGA-D3-A51G-10A-01D-A25O-08 | g.chr3:114069131G>A | c.1794C>T | c.(1792-1794)ttC>ttT | p.F598F |
SKCM | 3 | 114069353 | 114069353 | + | Silent | SNP | G | G | A | TCGA-EE-A2MD-06A-11D-A197-08 | TCGA-EE-A2MD-10A-01D-A199-08 | g.chr3:114069353G>A | c.1572C>T | c.(1570-1572)ttC>ttT | p.F524F |
SKCM | 3 | 114069374 | 114069374 | + | Silent | SNP | C | C | G | TCGA-ER-A19P-06A-11D-A196-08 | TCGA-ER-A19P-10A-01D-A198-08 | g.chr3:114069374C>G | c.1551G>C | c.(1549-1551)gcG>gcC | p.A517A |
SKCM | 3 | 114069466 | 114069466 | + | Silent | SNP | G | G | A | TCGA-EE-A2MD-06A-11D-A197-08 | TCGA-EE-A2MD-10A-01D-A199-08 | g.chr3:114069466G>A | c.1459C>T | c.(1459-1461)Ctg>Ttg | p.L487L |
SKCM | 3 | 114069569 | 114069569 | + | Silent | SNP | G | G | A | TCGA-EE-A2GC-06A-11D-A197-08 | TCGA-EE-A2GC-10A-01D-A199-08 | g.chr3:114069569G>A | c.1356C>T | c.(1354-1356)tcC>tcT | p.S452S |
SKCM | 3 | 114069633 | 114069633 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3AE-06A-11D-A196-08 | TCGA-EE-A3AE-10A-01D-A198-08 | g.chr3:114069633G>A | c.1292C>T | c.(1291-1293)tCc>tTc | p.S431F |
SKCM | 3 | 114069714 | 114069714 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MD-06A-11D-A197-08 | TCGA-EE-A2MD-10A-01D-A199-08 | g.chr3:114069714G>A | c.1211C>T | c.(1210-1212)gCt>gTt | p.A404V |
SKCM | 3 | 114069779 | 114069779 | + | Silent | SNP | G | G | A | TCGA-EE-A3JD-06A-11D-A20D-08 | TCGA-EE-A3JD-10A-01D-A20D-08 | g.chr3:114069779G>A | c.1146C>T | c.(1144-1146)tcC>tcT | p.S382S |
SKCM | 3 | 114069795 | 114069795 | + | Missense_Mutation | SNP | G | G | A | TCGA-ER-A193-06A-12D-A197-08 | TCGA-ER-A193-10A-01D-A199-08 | g.chr3:114069795G>A | c.1130C>T | c.(1129-1131)tCg>tTg | p.S377L |
SKCM | 3 | 114070173 | 114070173 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A51J-06A-11D-A25O-08 | TCGA-D3-A51J-10A-01D-A25O-08 | g.chr3:114070173G>A | c.752C>T | c.(751-753)tCc>tTc | p.S251F |
SKCM | 3 | 114070395 | 114070395 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MU-06A-21D-A196-08 | TCGA-EE-A2MU-10A-01D-A198-08 | g.chr3:114070395G>A | c.530C>T | c.(529-531)gCc>gTc | p.A177V |
SKCM | 3 | 114070414 | 114070414 | + | Silent | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr3:114070414G>A | c.511C>T | c.(511-513)Ctg>Ttg | p.L171L |
SKCM | 3 | 114070718 | 114070718 | + | Silent | SNP | G | G | A | TCGA-D3-A3C7-06A-11D-A196-08 | TCGA-D3-A3C7-10A-01D-A198-08 | g.chr3:114070718G>A | c.207C>T | c.(205-207)atC>atT | p.I69I |