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 | 23 | 40982957 | 40982957 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-OR-A5J5-01A-11D-A29I-10 | TCGA-OR-A5J5-10A-01D-A29L-10 | g.chrX:40982957delC | c.76delC | c.(76-78)cccfs | p.P27fs |
ACC | 23 | 41025466 | 41025466 | + | Splice_Site | SNP | G | G | C | TCGA-OR-A5KB-01A-11D-A30A-10 | TCGA-OR-A5KB-11A-11D-A30A-10 | g.chrX:41025466G>C | c.2327G>C | c.(2326-2328)aGg>aCg | p.R776T |
ACC | 23 | 41075161 | 41075161 | + | Missense_Mutation | SNP | G | G | A | TCGA-OR-A5LJ-01A-11D-A29I-10 | TCGA-OR-A5LJ-10A-01D-A29L-10 | g.chrX:41075161G>A | c.5341G>A | c.(5341-5343)Gta>Ata | p.V1781I |
BLCA | 23 | 41007694 | 41007694 | + | Missense_Mutation | SNP | G | G | A | TCGA-FD-A3SS-01A-12D-A22Z-08 | TCGA-FD-A3SS-10A-01D-A22Z-08 | g.chrX:41007694G>A | c.1492G>A | c.(1492-1494)Gat>Aat | p.D498N |
BLCA | 23 | 41010204 | 41010204 | + | Missense_Mutation | SNP | G | G | C | TCGA-DK-A3X1-01A-12D-A22Z-08 | TCGA-DK-A3X1-10A-01D-A22Z-08 | g.chrX:41010204G>C | c.1657G>C | c.(1657-1659)Gat>Cat | p.D553H |
BLCA | 23 | 41025165 | 41025165 | + | Missense_Mutation | SNP | C | C | G | TCGA-DK-A6B6-01A-11D-A30E-08 | TCGA-DK-A6B6-10A-01D-A30H-08 | g.chrX:41025165C>G | c.2026C>G | c.(2026-2028)Cag>Gag | p.Q676E |
BLCA | 23 | 41027283 | 41027283 | + | Missense_Mutation | SNP | T | T | G | TCGA-UY-A9PB-01A-11D-A38G-08 | TCGA-UY-A9PB-10A-01D-A38J-08 | g.chrX:41027283T>G | c.2448T>G | c.(2446-2448)atT>atG | p.I816M |
BLCA | 23 | 41027293 | 41027293 | + | Missense_Mutation | SNP | T | T | G | TCGA-UY-A9PB-01A-11D-A38G-08 | TCGA-UY-A9PB-10A-01D-A38J-08 | g.chrX:41027293T>G | c.2458T>G | c.(2458-2460)Ttt>Gtt | p.F820V |
BLCA | 23 | 41027317 | 41027317 | + | Missense_Mutation | SNP | G | G | A | TCGA-4Z-AA7R-01A-11D-A391-08 | TCGA-4Z-AA7R-10A-01D-A394-08 | g.chrX:41027317G>A | c.2482G>A | c.(2482-2484)Gac>Aac | p.D828N |
BLCA | 23 | 41029374 | 41029374 | + | Silent | SNP | T | T | C | TCGA-XF-A9T6-01A-11D-A42E-08 | TCGA-XF-A9T6-10A-01D-A42H-08 | g.chrX:41029374T>C | c.2763T>C | c.(2761-2763)aaT>aaC | p.N921N |
BLCA | 23 | 41029731 | 41029731 | + | Silent | SNP | A | A | T | TCGA-UY-A9PE-01A-11D-A38G-08 | TCGA-UY-A9PE-10A-01D-A38J-08 | g.chrX:41029731A>T | c.2886A>T | c.(2884-2886)acA>acT | p.T962T |
BLCA | 23 | 41047252 | 41047252 | + | Missense_Mutation | SNP | G | G | C | TCGA-4Z-AA86-01A-11D-A391-08 | TCGA-4Z-AA86-10A-01D-A394-08 | g.chrX:41047252G>C | c.3692G>C | c.(3691-3693)aGa>aCa | p.R1231T |
BLCA | 23 | 41047370 | 41047371 | + | Splice_Site | INS | - | - | GT | TCGA-BT-A2LB-01A-11D-A18F-08 | TCGA-BT-A2LB-10A-01D-A18F-08 | g.chrX:41047370_41047371insGT | c.3810_3810insGT | c.(3811-3813)acc>acGTc | p.T1271fs |
BLCA | 23 | 41056737 | 41056737 | + | Missense_Mutation | SNP | G | G | A | TCGA-ZF-AA54-01A-11D-A391-08 | TCGA-ZF-AA54-10A-01D-A394-08 | g.chrX:41056737G>A | c.4354G>A | c.(4354-4356)Gaa>Aaa | p.E1452K |
BLCA | 23 | 41057842 | 41057842 | + | Missense_Mutation | SNP | G | G | A | TCGA-GC-A6I1-01A-12D-A31L-08 | TCGA-GC-A6I1-10A-01D-A31J-08 | g.chrX:41057842G>A | c.4442G>A | c.(4441-4443)gGa>gAa | p.G1481E |
BLCA | 23 | 41060386 | 41060386 | + | Silent | SNP | G | G | C | TCGA-XF-AAMZ-01A-11D-A42E-08 | TCGA-XF-AAMZ-10A-01D-A42H-08 | g.chrX:41060386G>C | c.4677G>C | c.(4675-4677)ctG>ctC | p.L1559L |
BLCA | 23 | 41060455 | 41060455 | + | Missense_Mutation | SNP | G | G | C | TCGA-XF-A9SY-01A-21D-A42E-08 | TCGA-XF-A9SY-10A-01D-A42H-08 | g.chrX:41060455G>C | c.4746G>C | c.(4744-4746)agG>agC | p.R1582S |
BLCA | 23 | 41075732 | 41075732 | + | Missense_Mutation | SNP | A | A | G | TCGA-BT-A3PK-01A-21D-A21Z-08 | TCGA-BT-A3PK-10A-01D-A21Z-08 | g.chrX:41075732A>G | c.5912A>G | c.(5911-5913)gAg>gGg | p.E1971G |
BLCA | 23 | 41077663 | 41077663 | + | Missense_Mutation | SNP | A | A | T | TCGA-BT-A0YX-01A-11D-A10S-08 | TCGA-BT-A0YX-10A-01D-A10S-08 | g.chrX:41077663A>T | c.6248A>T | c.(6247-6249)aAt>aTt | p.N2083I |
BLCA | 23 | 41084104 | 41084104 | + | Missense_Mutation | SNP | G | G | C | TCGA-ZF-A9R7-01A-11D-A38G-08 | TCGA-ZF-A9R7-10A-01D-A38J-08 | g.chrX:41084104G>C | c.6861G>C | c.(6859-6861)aaG>aaC | p.K2287N |
BLCA | 23 | 41088555 | 41088555 | + | Missense_Mutation | SNP | G | G | C | TCGA-UY-A9PB-01A-11D-A38G-08 | TCGA-UY-A9PB-10A-01D-A38J-08 | g.chrX:41088555G>C | c.7111G>C | c.(7111-7113)Gac>Cac | p.D2371H |
BRCA | 23 | 40990740 | 40990741 | + | Frame_Shift_Del | DEL | AG | AG | - | TCGA-A2-A1FV-01A-11D-A13L-09 | TCGA-A2-A1FV-10A-01D-A13O-09 | g.chrX:40990740_40990741delAG | c.273_274delAG | c.(271-276)aaagggfs | p.G92fs |
BRCA | 23 | 40990750 | 40990750 | + | Missense_Mutation | SNP | G | G | C | TCGA-AC-A23H-01A-11D-A159-09 | TCGA-AC-A23H-11A-12D-A17G-09 | g.chrX:40990750G>C | c.283G>C | c.(283-285)Gaa>Caa | p.E95Q |
BRCA | 23 | 41007789 | 41007789 | + | Silent | SNP | C | C | T | TCGA-AR-A2LE-01A-11D-A17W-09 | TCGA-AR-A2LE-10A-01D-A17W-09 | g.chrX:41007789C>T | c.1587C>T | c.(1585-1587)ctC>ctT | p.L529L |
BRCA | 23 | 41010191 | 41010191 | + | Missense_Mutation | SNP | G | G | T | TCGA-AN-A046-01A-21W-A050-09 | TCGA-AN-A046-10A-01W-A055-09 | g.chrX:41010191G>T | c.1644G>T | c.(1642-1644)aaG>aaT | p.K548N |
BRCA | 23 | 41012240 | 41012240 | + | Silent | SNP | C | C | T | TCGA-D8-A1XZ-01A-11D-A14K-09 | TCGA-D8-A1XZ-10A-01D-A14K-09 | g.chrX:41012240C>T | c.1803C>T | c.(1801-1803)gaC>gaT | p.D601D |
BRCA | 23 | 41025364 | 41025364 | + | Missense_Mutation | SNP | G | G | A | TCGA-B6-A0X7-01A-11D-A10M-09 | TCGA-B6-A0X7-10A-01D-A10M-09 | g.chrX:41025364G>A | c.2225G>A | c.(2224-2226)cGa>cAa | p.R742Q |
BRCA | 23 | 41025387 | 41025387 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-D8-A1X7-01A-11D-A14K-09 | TCGA-D8-A1X7-10A-01D-A14K-09 | g.chrX:41025387C>T | c.2248C>T | c.(2248-2250)Cga>Tga | p.R750* |
BRCA | 23 | 41043849 | 41043849 | + | Missense_Mutation | SNP | C | C | G | TCGA-E9-A1RF-01A-11D-A159-09 | TCGA-E9-A1RF-10A-01D-A159-09 | g.chrX:41043849C>G | c.3479C>G | c.(3478-3480)aCt>aGt | p.T1160S |
BRCA | 23 | 41047365 | 41047365 | + | Missense_Mutation | SNP | G | G | C | TCGA-C8-A26Y-01A-11D-A16D-09 | TCGA-C8-A26Y-10A-01D-A16D-09 | g.chrX:41047365G>C | c.3805G>C | c.(3805-3807)Gag>Cag | p.E1269Q |
BRCA | 23 | 41048627 | 41048627 | + | Missense_Mutation | SNP | G | G | A | TCGA-BH-A18U-01A-21D-A12B-09 | TCGA-BH-A18U-11A-23D-A12B-09 | g.chrX:41048627G>A | c.3876G>A | c.(3874-3876)atG>atA | p.M1292I |
BRCA | 23 | 41048632 | 41048633 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-AN-A0XN-01A-21D-A10G-09 | TCGA-AN-A0XN-10A-01D-A10G-09 | g.chrX:41048632_41048633insA | c.3881_3882insA | c.(3880-3885)ttatgtfs | p.C1295fs |
BRCA | 23 | 41048645 | 41048645 | + | Missense_Mutation | SNP | G | G | C | TCGA-AC-A23H-01A-11D-A159-09 | TCGA-AC-A23H-11A-12D-A17G-09 | g.chrX:41048645G>C | c.3894G>C | c.(3892-3894)ttG>ttC | p.L1298F |
BRCA | 23 | 41055854 | 41055855 | + | Frame_Shift_Del | DEL | AG | AG | - | TCGA-BH-A18G-01A-11D-A12B-09 | TCGA-BH-A18G-10A-01D-A12B-09 | g.chrX:41055854_41055855delAG | c.4096_4097delAG | c.(4096-4098)agafs | p.R1366fs |
BRCA | 23 | 41056704 | 41056704 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-EW-A1J5-01A-11D-A13L-09 | TCGA-EW-A1J5-10A-01D-A13O-09 | g.chrX:41056704C>T | c.4321C>T | c.(4321-4323)Caa>Taa | p.Q1441* |
BRCA | 23 | 41073963 | 41073963 | + | Splice_Site | SNP | G | G | A | TCGA-AC-A2FM-01A-11D-A19Y-09 | TCGA-AC-A2FM-11B-32D-A19Y-09 | g.chrX:41073963G>A | | c.e34+1 | |
BRCA | 23 | 41075185 | 41075185 | + | Silent | SNP | T | T | C | TCGA-A2-A0T3-01A-21D-A10Y-09 | TCGA-A2-A0T3-10A-01D-A110-09 | g.chrX:41075185T>C | c.5365T>C | c.(5365-5367)Tta>Cta | p.L1789L |
BRCA | 23 | 41075313 | 41075313 | + | Silent | SNP | T | T | G | TCGA-A8-A0A6-01A-12W-A071-09 | TCGA-A8-A0A6-10A-01W-A071-09 | g.chrX:41075313T>G | c.5493T>G | c.(5491-5493)ggT>ggG | p.G1831G |
BRCA | 23 | 41075620 | 41075620 | + | Missense_Mutation | SNP | A | A | C | TCGA-GM-A2DB-01A-31D-A19Y-09 | TCGA-GM-A2DB-10C-01D-A18P-09 | g.chrX:41075620A>C | c.5800A>C | c.(5800-5802)Atg>Ctg | p.M1934L |
BRCA | 23 | 41075653 | 41075653 | + | Missense_Mutation | SNP | T | T | G | TCGA-A8-A0A6-01A-12W-A071-09 | TCGA-A8-A0A6-10A-01W-A071-09 | g.chrX:41075653T>G | c.5833T>G | c.(5833-5835)Tgg>Ggg | p.W1945G |
BRCA | 23 | 41076559 | 41076559 | + | Missense_Mutation | SNP | C | C | G | TCGA-AN-A0G0-01A-11W-A050-09 | TCGA-AN-A0G0-10A-01W-A055-09 | g.chrX:41076559C>G | c.6172C>G | c.(6172-6174)Cac>Gac | p.H2058D |
BRCA | 23 | 41082490 | 41082490 | + | Missense_Mutation | SNP | C | C | G | TCGA-A7-A26J-01A-11D-A167-09 | TCGA-A7-A26J-10A-01D-A167-09 | g.chrX:41082490C>G | c.6586C>G | c.(6586-6588)Ctt>Gtt | p.L2196V |
BRCA | 23 | 41084197 | 41084198 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-AO-A12H-01A-11D-A10Y-09 | TCGA-AO-A12H-10A-01D-A110-09 | g.chrX:41084197_41084198insA | c.6954_6955insA | c.(6955-6957)agtfs | p.S2319fs |
CESC | 23 | 40999952 | 40999952 | + | Missense_Mutation | SNP | G | G | A | TCGA-EA-A3HU-01A-11D-A20U-09 | TCGA-EA-A3HU-10B-01D-A20U-09 | g.chrX:40999952G>A | c.698G>A | c.(697-699)gGg>gAg | p.G233E |
CESC | 23 | 41029361 | 41029361 | + | Missense_Mutation | SNP | G | G | A | TCGA-C5-A3HE-01A-21D-A22X-09 | TCGA-C5-A3HE-10A-01D-A22X-09 | g.chrX:41029361G>A | c.2750G>A | c.(2749-2751)cGa>cAa | p.R917Q |
CESC | 23 | 41043695 | 41043695 | + | Missense_Mutation | SNP | G | G | A | TCGA-JW-A852-01A-11D-A351-09 | TCGA-JW-A852-10A-01D-A351-09 | g.chrX:41043695G>A | c.3325G>A | c.(3325-3327)Gat>Aat | p.D1109N |
CESC | 23 | 41047349 | 41047350 | + | Frame_Shift_Ins | INS | - | - | TT | TCGA-EK-A2PM-01A-11D-A18J-09 | TCGA-EK-A2PM-10A-01D-A18J-09 | g.chrX:41047349_41047350insTT | c.3789_3790insTT | c.(3790-3792)atcfs | p.I1264fs |
CESC | 23 | 41055534 | 41055534 | + | Missense_Mutation | SNP | C | C | A | TCGA-FU-A3HZ-01A-11D-A20U-09 | TCGA-FU-A3HZ-10A-01D-A20U-09 | g.chrX:41055534C>A | c.4008C>A | c.(4006-4008)ttC>ttA | p.F1336L |
CESC | 23 | 41055965 | 41055965 | + | Missense_Mutation | SNP | G | G | A | TCGA-C5-A3HD-01B-11D-A20U-09 | TCGA-C5-A3HD-10A-01D-A20U-09 | g.chrX:41055965G>A | c.4207G>A | c.(4207-4209)Gaa>Aaa | p.E1403K |
CESC | 23 | 41075524 | 41075524 | + | Missense_Mutation | SNP | G | G | A | TCGA-EA-A439-01A-11D-A243-09 | TCGA-EA-A439-10A-01D-A243-09 | g.chrX:41075524G>A | c.5704G>A | c.(5704-5706)Gat>Aat | p.D1902N |
CESC | 23 | 41077746 | 41077746 | + | Missense_Mutation | SNP | G | G | A | TCGA-C5-A1BM-01A-11D-A13W-08 | TCGA-C5-A1BM-10A-01D-A13W-08 | g.chrX:41077746G>A | c.6331G>A | c.(6331-6333)Gaa>Aaa | p.E2111K |
CESC | 23 | 41089034 | 41089035 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-EA-A3HU-01A-11D-A20U-09 | TCGA-EA-A3HU-10B-01D-A20U-09 | g.chrX:41089034_41089035insA | c.7433_7434insA | c.(7432-7437)gtaaaafs | p.VK2478fs |
CHOL | 23 | 41043819 | 41043819 | + | Missense_Mutation | SNP | A | A | G | TCGA-W5-AA33-01A-11D-A417-09 | TCGA-W5-AA33-10A-01D-A41A-09 | g.chrX:41043819A>G | c.3449A>G | c.(3448-3450)aAt>aGt | p.N1150S |
CHOL | 23 | 41088540 | 41088540 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-ZU-A8S4-01A-11D-A417-09 | TCGA-ZU-A8S4-10A-01D-A41A-09 | g.chrX:41088540C>T | c.7096C>T | c.(7096-7098)Cga>Tga | p.R2366* |
COAD | 23 | 40982912 | 40982912 | + | Missense_Mutation | SNP | G | G | A | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chrX:40982912G>A | c.31G>A | c.(31-33)Gga>Aga | p.G11R |
COAD | 23 | 40988350 | 40988350 | + | Missense_Mutation | SNP | C | C | A | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chrX:40988350C>A | c.194C>A | c.(193-195)cCt>cAt | p.P65H |
COAD | 23 | 40988387 | 40988387 | + | Silent | SNP | C | C | T | TCGA-AA-3710-01A-01W-0995-10 | TCGA-AA-3710-10A-01W-0995-10 | g.chrX:40988387C>T | c.231C>T | c.(229-231)gaC>gaT | p.D77D |
COAD | 23 | 40990744 | 40990744 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-A6-5660-01A-01D-1650-10 | TCGA-A6-5660-10A-01D-1650-10 | g.chrX:40990744G>T | c.277G>T | c.(277-279)Gaa>Taa | p.E93* |
COAD | 23 | 40996081 | 40996081 | + | Missense_Mutation | SNP | C | C | T | TCGA-CM-6680-01A-11D-1835-10 | TCGA-CM-6680-10A-01D-1835-10 | g.chrX:40996081C>T | c.460C>T | c.(460-462)Cgt>Tgt | p.R154C |
COAD | 23 | 41000437 | 41000437 | + | Missense_Mutation | SNP | A | A | C | TCGA-CK-4950-01A-01D-1719-10 | TCGA-CK-4950-10A-01D-1719-10 | g.chrX:41000437A>C | c.989A>C | c.(988-990)aAc>aCc | p.N330T |
COAD | 23 | 41010222 | 41010222 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chrX:41010222C>A | c.1675C>A | c.(1675-1677)Ctt>Att | p.L559I |
COAD | 23 | 41022042 | 41022042 | + | Splice_Site | SNP | G | G | A | TCGA-CM-6165-01A-11D-1650-10 | TCGA-CM-6165-10A-01D-1650-10 | g.chrX:41022042G>A | | c.e15-1 | |
COAD | 23 | 41025167 | 41025167 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3811-01A-01W-0995-10 | TCGA-AA-3811-10A-01W-0995-10 | g.chrX:41025167G>T | c.2028G>T | c.(2026-2028)caG>caT | p.Q676H |
COAD | 23 | 41025219 | 41025219 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3864-01A-01W-0995-10 | TCGA-AA-3864-10A-01W-0995-10 | g.chrX:41025219C>T | c.2080C>T | c.(2080-2082)Cgt>Tgt | p.R694C |
COAD | 23 | 41025392 | 41025392 | + | Missense_Mutation | SNP | A | A | C | TCGA-A6-5665-01A-01D-1650-10 | TCGA-A6-5665-10A-01D-1650-10 | g.chrX:41025392A>C | c.2253A>C | c.(2251-2253)gaA>gaC | p.E751D |
COAD | 23 | 41027380 | 41027380 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chrX:41027380C>T | c.2545C>T | c.(2545-2547)Cga>Tga | p.R849* |
COAD | 23 | 41029361 | 41029361 | + | Missense_Mutation | SNP | G | G | A | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chrX:41029361G>A | c.2750G>A | c.(2749-2751)cGa>cAa | p.R917Q |
COAD | 23 | 41045782 | 41045782 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chrX:41045782A>G | c.3571A>G | c.(3571-3573)Acc>Gcc | p.T1191A |
COAD | 23 | 41045841 | 41045841 | + | Silent | SNP | C | C | T | TCGA-AA-3518-01A-02W-0833-10 | TCGA-AA-3518-10A-01W-0833-10 | g.chrX:41045841C>T | c.3630C>T | c.(3628-3630)tcC>tcT | p.S1210S |
COAD | 23 | 41047291 | 41047291 | + | Missense_Mutation | SNP | A | A | C | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chrX:41047291A>C | c.3731A>C | c.(3730-3732)aAa>aCa | p.K1244T |
COAD | 23 | 41055599 | 41055599 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3492-01A-01D-1408-10 | TCGA-AA-3492-11A-01D-1408-10 | g.chrX:41055599T>C | c.4073T>C | c.(4072-4074)tTt>tCt | p.F1358S |
COAD | 23 | 41055978 | 41055978 | + | Missense_Mutation | SNP | T | T | G | TCGA-CM-5864-01A-01D-1650-10 | TCGA-CM-5864-10A-01D-1650-10 | g.chrX:41055978T>G | c.4220T>G | c.(4219-4221)cTt>cGt | p.L1407R |
COAD | 23 | 41057839 | 41057839 | + | Missense_Mutation | SNP | A | A | C | TCGA-CM-5864-01A-01D-1650-10 | TCGA-CM-5864-10A-01D-1650-10 | g.chrX:41057839A>C | c.4439A>C | c.(4438-4440)aAt>aCt | p.N1480T |
COAD | 23 | 41064704 | 41064704 | + | Missense_Mutation | SNP | G | G | A | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chrX:41064704G>A | c.4973G>A | c.(4972-4974)cGa>cAa | p.R1658Q |
COAD | 23 | 41069809 | 41069809 | + | Missense_Mutation | SNP | A | A | C | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chrX:41069809A>C | c.5063A>C | c.(5062-5064)gAa>gCa | p.E1688A |
COAD | 23 | 41073882 | 41073882 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chrX:41073882C>A | c.5251C>A | c.(5251-5253)Ctt>Att | p.L1751I |
COAD | 23 | 41073946 | 41073946 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-CK-5913-01A-11D-1650-10 | TCGA-CK-5913-10A-01D-1650-10 | g.chrX:41073946delA | c.5315delA | c.(5314-5316)gaafs | p.E1772fs |
COAD | 23 | 41075428 | 41075428 | + | Missense_Mutation | SNP | G | G | A | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chrX:41075428G>A | c.5608G>A | c.(5608-5610)Gta>Ata | p.V1870I |
COAD | 23 | 41075439 | 41075439 | + | Silent | SNP | T | T | G | TCGA-AA-3966-01A-01W-1073-09 | TCGA-AA-3966-10A-01W-1073-09 | g.chrX:41075439T>G | c.5619T>G | c.(5617-5619)ggT>ggG | p.G1873G |
COAD | 23 | 41075506 | 41075506 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3510-01A-01D-1408-10 | TCGA-AA-3510-11A-01D-1408-10 | g.chrX:41075506C>T | c.5686C>T | c.(5686-5688)Cgc>Tgc | p.R1896C |
COAD | 23 | 41075555 | 41075555 | + | Missense_Mutation | SNP | A | A | G | TCGA-D5-6537-01A-11D-1719-10 | TCGA-D5-6537-10A-01D-1719-10 | g.chrX:41075555A>G | c.5735A>G | c.(5734-5736)gAt>gGt | p.D1912G |
COAD | 23 | 41075555 | 41075555 | + | Missense_Mutation | SNP | A | A | G | TCGA-D5-6898-01A-11D-1924-10 | TCGA-D5-6898-10A-01D-1924-10 | g.chrX:41075555A>G | c.5735A>G | c.(5734-5736)gAt>gGt | p.D1912G |
COAD | 23 | 41075559 | 41075559 | + | Silent | SNP | C | C | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chrX:41075559C>T | c.5739C>T | c.(5737-5739)gaC>gaT | p.D1913D |
COAD | 23 | 41075672 | 41075672 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-D5-6538-01A-11D-1719-10 | TCGA-D5-6538-10A-01D-1719-10 | g.chrX:41075672delT | c.5852delT | c.(5851-5853)cttfs | p.L1951fs |
COAD | 23 | 41075683 | 41075683 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-AA-3815-01A-01W-0995-10 | TCGA-AA-3815-10A-01W-0995-10 | g.chrX:41075683C>T | c.5863C>T | c.(5863-5865)Cga>Tga | p.R1955* |
COAD | 23 | 41076578 | 41076578 | + | Missense_Mutation | SNP | G | G | A | TCGA-CM-6162-01A-11D-1650-10 | TCGA-CM-6162-10A-01D-1650-10 | g.chrX:41076578G>A | c.6191G>A | c.(6190-6192)cGt>cAt | p.R2064H |
COAD | 23 | 41077661 | 41077661 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3713-01A-21D-1719-10 | TCGA-AA-3713-11A-01D-1719-10 | g.chrX:41077661G>T | c.6246G>T | c.(6244-6246)aaG>aaT | p.K2082N |
COAD | 23 | 41078483 | 41078483 | + | Splice_Site | SNP | A | A | T | TCGA-AZ-4682-01B-01D-1408-10 | TCGA-AZ-4682-10A-01D-1408-10 | g.chrX:41078483A>T | c.6564A>T | c.(6562-6564)ttA>ttT | p.L2188F |
COAD | 23 | 41082527 | 41082527 | + | Missense_Mutation | SNP | T | T | C | TCGA-F4-6570-01A-11D-1771-10 | TCGA-F4-6570-10A-01D-1771-10 | g.chrX:41082527T>C | c.6623T>C | c.(6622-6624)gTg>gCg | p.V2208A |
COAD | 23 | 41084097 | 41084097 | + | Missense_Mutation | SNP | A | A | G | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chrX:41084097A>G | c.6854A>G | c.(6853-6855)tAt>tGt | p.Y2285C |
COAD | 23 | 41088571 | 41088572 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-CK-5912-01A-11D-1650-10 | TCGA-CK-5912-10A-01D-1650-10 | g.chrX:41088571_41088572insT | c.7127_7128insT | c.(7126-7131)tctaagfs | p.K2377fs |
COAD | 23 | 41088663 | 41088663 | + | Splice_Site | SNP | G | G | A | TCGA-CM-5862-01A-01D-1650-10 | TCGA-CM-5862-10A-01D-1650-10 | g.chrX:41088663G>A | | c.e42+1 | |
COAD | 23 | 41089034 | 41089035 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-AA-3864-01A-01W-0995-10 | TCGA-AA-3864-10A-01W-0995-10 | g.chrX:41089034_41089035insA | c.7433_7434insA | c.(7432-7437)gtaaaafs | p.VK2478fs |
COAD | 23 | 41089035 | 41089035 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-AA-3715-01A-01W-0900-09 | TCGA-AA-3715-10A-01W-0900-09 | g.chrX:41089035delA | c.7434delA | c.(7432-7434)gtafs | p.V2478fs |
COAD | 23 | 41089035 | 41089035 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-AA-3815-01A-01W-0995-10 | TCGA-AA-3815-10A-01W-0995-10 | g.chrX:41089035delA | c.7434delA | c.(7432-7434)gtafs | p.V2478fs |
COAD | 23 | 41089035 | 41089035 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-CK-5913-01A-11D-1650-10 | TCGA-CK-5913-10A-01D-1650-10 | g.chrX:41089035delA | c.7434delA | c.(7432-7434)gtafs | p.V2478fs |
COAD | 23 | 41089035 | 41089035 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-F4-6856-01A-11D-1924-10 | TCGA-F4-6856-10A-01D-1924-10 | g.chrX:41089035delA | c.7434delA | c.(7432-7434)gtafs | p.V2478fs |
COAD | 23 | 41091690 | 41091690 | + | Missense_Mutation | SNP | G | G | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chrX:41091690G>T | c.7626G>T | c.(7624-7626)atG>atT | p.M2542I |
COADREAD | 23 | 40982912 | 40982912 | + | Missense_Mutation | SNP | G | G | A | TCGA-AZ-6598-01A-11D-1771-10 | TCGA-AZ-6598-11A-01D-1771-10 | g.chrX:40982912G>A | c.31G>A | c.(31-33)Gga>Aga | p.G11R |
COADREAD | 23 | 40988350 | 40988350 | + | Missense_Mutation | SNP | C | C | A | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chrX:40988350C>A | c.194C>A | c.(193-195)cCt>cAt | p.P65H |
COADREAD | 23 | 40988387 | 40988387 | + | Silent | SNP | C | C | T | TCGA-AA-3710-01A-01W-0995-10 | TCGA-AA-3710-10A-01W-0995-10 | g.chrX:40988387C>T | c.231C>T | c.(229-231)gaC>gaT | p.D77D |
COADREAD | 23 | 40990744 | 40990744 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-A6-5660-01A-01D-1650-10 | TCGA-A6-5660-10A-01D-1650-10 | g.chrX:40990744G>T | c.277G>T | c.(277-279)Gaa>Taa | p.E93* |
COADREAD | 23 | 40996081 | 40996081 | + | Missense_Mutation | SNP | C | C | T | TCGA-CM-6680-01A-11D-1835-10 | TCGA-CM-6680-10A-01D-1835-10 | g.chrX:40996081C>T | c.460C>T | c.(460-462)Cgt>Tgt | p.R154C |
COADREAD | 23 | 40996156 | 40996156 | + | Missense_Mutation | SNP | A | A | C | TCGA-AG-3892-01A-01W-1073-09 | TCGA-AG-3892-10A-01W-1073-09 | g.chrX:40996156A>C | c.535A>C | c.(535-537)Aat>Cat | p.N179H |
COADREAD | 23 | 41000437 | 41000437 | + | Missense_Mutation | SNP | A | A | C | TCGA-CK-4950-01A-01D-1719-10 | TCGA-CK-4950-10A-01D-1719-10 | g.chrX:41000437A>C | c.989A>C | c.(988-990)aAc>aCc | p.N330T |
COADREAD | 23 | 41007672 | 41007672 | + | Silent | SNP | G | G | A | TCGA-AG-A026-01A-32W-A096-10 | TCGA-AG-A026-10A-01W-A096-10 | g.chrX:41007672G>A | c.1470G>A | c.(1468-1470)ctG>ctA | p.L490L |
COADREAD | 23 | 41010222 | 41010222 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chrX:41010222C>A | c.1675C>A | c.(1675-1677)Ctt>Att | p.L559I |
COADREAD | 23 | 41022042 | 41022042 | + | Splice_Site | SNP | G | G | A | TCGA-CM-6165-01A-11D-1650-10 | TCGA-CM-6165-10A-01D-1650-10 | g.chrX:41022042G>A | | c.e15-1 | |
COADREAD | 23 | 41025167 | 41025167 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3811-01A-01W-0995-10 | TCGA-AA-3811-10A-01W-0995-10 | g.chrX:41025167G>T | c.2028G>T | c.(2026-2028)caG>caT | p.Q676H |
COADREAD | 23 | 41025219 | 41025219 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3864-01A-01W-0995-10 | TCGA-AA-3864-10A-01W-0995-10 | g.chrX:41025219C>T | c.2080C>T | c.(2080-2082)Cgt>Tgt | p.R694C |
COADREAD | 23 | 41025392 | 41025392 | + | Missense_Mutation | SNP | A | A | C | TCGA-A6-5665-01A-01D-1650-10 | TCGA-A6-5665-10A-01D-1650-10 | g.chrX:41025392A>C | c.2253A>C | c.(2251-2253)gaA>gaC | p.E751D |
COADREAD | 23 | 41027380 | 41027380 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chrX:41027380C>T | c.2545C>T | c.(2545-2547)Cga>Tga | p.R849* |
COADREAD | 23 | 41029361 | 41029361 | + | Missense_Mutation | SNP | G | G | A | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chrX:41029361G>A | c.2750G>A | c.(2749-2751)cGa>cAa | p.R917Q |
COADREAD | 23 | 41045782 | 41045782 | + | Missense_Mutation | SNP | A | A | G | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chrX:41045782A>G | c.3571A>G | c.(3571-3573)Acc>Gcc | p.T1191A |
COADREAD | 23 | 41045841 | 41045841 | + | Silent | SNP | C | C | T | TCGA-AA-3518-01A-02W-0833-10 | TCGA-AA-3518-10A-01W-0833-10 | g.chrX:41045841C>T | c.3630C>T | c.(3628-3630)tcC>tcT | p.S1210S |
COADREAD | 23 | 41047291 | 41047291 | + | Missense_Mutation | SNP | A | A | C | TCGA-AA-A00N-01A-02W-A00E-09 | TCGA-AA-A00N-10A-01W-A00E-09 | g.chrX:41047291A>C | c.3731A>C | c.(3730-3732)aAa>aCa | p.K1244T |
COADREAD | 23 | 41055599 | 41055599 | + | Missense_Mutation | SNP | T | T | C | TCGA-AA-3492-01A-01D-1408-10 | TCGA-AA-3492-11A-01D-1408-10 | g.chrX:41055599T>C | c.4073T>C | c.(4072-4074)tTt>tCt | p.F1358S |
COADREAD | 23 | 41055978 | 41055978 | + | Missense_Mutation | SNP | T | T | G | TCGA-CM-5864-01A-01D-1650-10 | TCGA-CM-5864-10A-01D-1650-10 | g.chrX:41055978T>G | c.4220T>G | c.(4219-4221)cTt>cGt | p.L1407R |
COADREAD | 23 | 41057839 | 41057839 | + | Missense_Mutation | SNP | A | A | C | TCGA-CM-5864-01A-01D-1650-10 | TCGA-CM-5864-10A-01D-1650-10 | g.chrX:41057839A>C | c.4439A>C | c.(4438-4440)aAt>aCt | p.N1480T |
COADREAD | 23 | 41064704 | 41064704 | + | Missense_Mutation | SNP | G | G | A | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chrX:41064704G>A | c.4973G>A | c.(4972-4974)cGa>cAa | p.R1658Q |
COADREAD | 23 | 41069809 | 41069809 | + | Missense_Mutation | SNP | A | A | C | TCGA-CA-6718-01A-11D-1835-10 | TCGA-CA-6718-10A-01D-1835-10 | g.chrX:41069809A>C | c.5063A>C | c.(5062-5064)gAa>gCa | p.E1688A |
COADREAD | 23 | 41073882 | 41073882 | + | Missense_Mutation | SNP | C | C | A | TCGA-AA-3984-01A-02W-0995-10 | TCGA-AA-3984-10A-01W-0999-10 | g.chrX:41073882C>A | c.5251C>A | c.(5251-5253)Ctt>Att | p.L1751I |
COADREAD | 23 | 41073946 | 41073946 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-CK-5913-01A-11D-1650-10 | TCGA-CK-5913-10A-01D-1650-10 | g.chrX:41073946delA | c.5315delA | c.(5314-5316)gaafs | p.E1772fs |
COADREAD | 23 | 41075428 | 41075428 | + | Missense_Mutation | SNP | G | G | A | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chrX:41075428G>A | c.5608G>A | c.(5608-5610)Gta>Ata | p.V1870I |
COADREAD | 23 | 41075439 | 41075439 | + | Silent | SNP | T | T | G | TCGA-AA-3966-01A-01W-1073-09 | TCGA-AA-3966-10A-01W-1073-09 | g.chrX:41075439T>G | c.5619T>G | c.(5617-5619)ggT>ggG | p.G1873G |
COADREAD | 23 | 41075506 | 41075506 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3510-01A-01D-1408-10 | TCGA-AA-3510-11A-01D-1408-10 | g.chrX:41075506C>T | c.5686C>T | c.(5686-5688)Cgc>Tgc | p.R1896C |
COADREAD | 23 | 41075555 | 41075555 | + | Missense_Mutation | SNP | A | A | G | TCGA-D5-6537-01A-11D-1719-10 | TCGA-D5-6537-10A-01D-1719-10 | g.chrX:41075555A>G | c.5735A>G | c.(5734-5736)gAt>gGt | p.D1912G |
COADREAD | 23 | 41075555 | 41075555 | + | Missense_Mutation | SNP | A | A | G | TCGA-D5-6898-01A-11D-1924-10 | TCGA-D5-6898-10A-01D-1924-10 | g.chrX:41075555A>G | c.5735A>G | c.(5734-5736)gAt>gGt | p.D1912G |
COADREAD | 23 | 41075559 | 41075559 | + | Silent | SNP | C | C | T | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chrX:41075559C>T | c.5739C>T | c.(5737-5739)gaC>gaT | p.D1913D |
COADREAD | 23 | 41075672 | 41075672 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-D5-6538-01A-11D-1719-10 | TCGA-D5-6538-10A-01D-1719-10 | g.chrX:41075672delT | c.5852delT | c.(5851-5853)cttfs | p.L1951fs |
COADREAD | 23 | 41075683 | 41075683 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-AA-3815-01A-01W-0995-10 | TCGA-AA-3815-10A-01W-0995-10 | g.chrX:41075683C>T | c.5863C>T | c.(5863-5865)Cga>Tga | p.R1955* |
COADREAD | 23 | 41076578 | 41076578 | + | Missense_Mutation | SNP | G | G | A | TCGA-CM-6162-01A-11D-1650-10 | TCGA-CM-6162-10A-01D-1650-10 | g.chrX:41076578G>A | c.6191G>A | c.(6190-6192)cGt>cAt | p.R2064H |
COADREAD | 23 | 41077661 | 41077661 | + | Missense_Mutation | SNP | G | G | T | TCGA-AA-3713-01A-21D-1719-10 | TCGA-AA-3713-11A-01D-1719-10 | g.chrX:41077661G>T | c.6246G>T | c.(6244-6246)aaG>aaT | p.K2082N |
COADREAD | 23 | 41078483 | 41078483 | + | Splice_Site | SNP | A | A | T | TCGA-AZ-4682-01B-01D-1408-10 | TCGA-AZ-4682-10A-01D-1408-10 | g.chrX:41078483A>T | c.6564A>T | c.(6562-6564)ttA>ttT | p.L2188F |
COADREAD | 23 | 41082527 | 41082527 | + | Missense_Mutation | SNP | T | T | C | TCGA-F4-6570-01A-11D-1771-10 | TCGA-F4-6570-10A-01D-1771-10 | g.chrX:41082527T>C | c.6623T>C | c.(6622-6624)gTg>gCg | p.V2208A |
COADREAD | 23 | 41084097 | 41084097 | + | Missense_Mutation | SNP | A | A | G | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chrX:41084097A>G | c.6854A>G | c.(6853-6855)tAt>tGt | p.Y2285C |
COADREAD | 23 | 41084340 | 41084340 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chrX:41084340G>T | c.7011G>T | c.(7009-7011)ttG>ttT | p.L2337F |
COADREAD | 23 | 41088571 | 41088572 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-CK-5912-01A-11D-1650-10 | TCGA-CK-5912-10A-01D-1650-10 | g.chrX:41088571_41088572insT | c.7127_7128insT | c.(7126-7131)tctaagfs | p.K2377fs |
COADREAD | 23 | 41088663 | 41088663 | + | Splice_Site | SNP | G | G | A | TCGA-CM-5862-01A-01D-1650-10 | TCGA-CM-5862-10A-01D-1650-10 | g.chrX:41088663G>A | | c.e42+1 | |
COADREAD | 23 | 41089034 | 41089035 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-AA-3864-01A-01W-0995-10 | TCGA-AA-3864-10A-01W-0995-10 | g.chrX:41089034_41089035insA | c.7433_7434insA | c.(7432-7437)gtaaaafs | p.VK2478fs |
COADREAD | 23 | 41089035 | 41089035 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-AA-3715-01A-01W-0900-09 | TCGA-AA-3715-10A-01W-0900-09 | g.chrX:41089035delA | c.7434delA | c.(7432-7434)gtafs | p.V2478fs |
COADREAD | 23 | 41089035 | 41089035 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-AA-3815-01A-01W-0995-10 | TCGA-AA-3815-10A-01W-0995-10 | g.chrX:41089035delA | c.7434delA | c.(7432-7434)gtafs | p.V2478fs |
COADREAD | 23 | 41089035 | 41089035 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-CK-5913-01A-11D-1650-10 | TCGA-CK-5913-10A-01D-1650-10 | g.chrX:41089035delA | c.7434delA | c.(7432-7434)gtafs | p.V2478fs |
COADREAD | 23 | 41089035 | 41089035 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-F4-6856-01A-11D-1924-10 | TCGA-F4-6856-10A-01D-1924-10 | g.chrX:41089035delA | c.7434delA | c.(7432-7434)gtafs | p.V2478fs |
COADREAD | 23 | 41091690 | 41091690 | + | Missense_Mutation | SNP | G | G | T | TCGA-AZ-4315-01A-01D-1408-10 | TCGA-AZ-4315-10A-01D-1408-10 | g.chrX:41091690G>T | c.7626G>T | c.(7624-7626)atG>atT | p.M2542I |
DLBC | 23 | 41056722 | 41056722 | + | Missense_Mutation | SNP | T | T | A | TCGA-FF-A7CR-01A-11D-A382-10 | TCGA-FF-A7CR-10A-01D-A385-10 | g.chrX:41056722T>A | c.4339T>A | c.(4339-4341)Ttt>Att | p.F1447I |
DLBC | 23 | 41075218 | 41075218 | + | Missense_Mutation | SNP | T | T | G | TCGA-GS-A9U3-01A-11D-A38X-10 | TCGA-GS-A9U3-10A-01D-A38X-10 | g.chrX:41075218T>G | c.5398T>G | c.(5398-5400)Ttt>Gtt | p.F1800V |
ESCA | 23 | 41000020 | 41000020 | + | Missense_Mutation | SNP | A | A | C | TCGA-M9-A5M8-01A-11D-A28B-09 | TCGA-M9-A5M8-10A-01D-A28E-09 | g.chrX:41000020A>C | c.766A>C | c.(766-768)Att>Ctt | p.I256L |
ESCA | 23 | 41007638 | 41007638 | + | Missense_Mutation | SNP | C | C | T | TCGA-L5-A891-01A-11D-A36J-09 | TCGA-L5-A891-11A-21D-A36M-09 | g.chrX:41007638C>T | c.1436C>T | c.(1435-1437)gCg>gTg | p.A479V |
ESCA | 23 | 41029818 | 41029818 | + | Silent | SNP | T | T | C | TCGA-L5-A4OI-01A-11D-A27G-09 | TCGA-L5-A4OI-11A-11D-A27G-09 | g.chrX:41029818T>C | c.2973T>C | c.(2971-2973)ggT>ggC | p.G991G |
ESCA | 23 | 41057781 | 41057781 | + | Splice_Site | SNP | G | G | T | TCGA-LN-A4A4-01A-11D-A27G-09 | TCGA-LN-A4A4-10A-01D-A27G-09 | g.chrX:41057781G>T | c.4381G>T | c.(4381-4383)Gaa>Taa | p.E1461* |
ESCA | 23 | 41057806 | 41057806 | + | Missense_Mutation | SNP | C | C | T | TCGA-ZR-A9CJ-01B-11D-A387-09 | TCGA-ZR-A9CJ-10A-01D-A38A-09 | g.chrX:41057806C>T | c.4406C>T | c.(4405-4407)cCt>cTt | p.P1469L |
ESCA | 23 | 41084051 | 41084051 | + | Missense_Mutation | SNP | C | C | T | TCGA-JY-A939-01A-12D-A37C-09 | TCGA-JY-A939-10A-01D-A37F-09 | g.chrX:41084051C>T | c.6808C>T | c.(6808-6810)Cca>Tca | p.P2270S |
GBM | 23 | 41075424 | 41075424 | + | Silent | SNP | G | G | A | TCGA-06-5412-01A-01D-1696-08 | TCGA-06-5412-10A-01D-1696-08 | g.chrX:41075424G>A | c.5604G>A | c.(5602-5604)gtG>gtA | p.V1868V |
GBM | 23 | 41075440 | 41075440 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-02-0047-01A-01D-1490-08 | TCGA-02-0047-10A-01D-1490-08 | g.chrX:41075440C>T | c.5620C>T | c.(5620-5622)Caa>Taa | p.Q1874* |
GBM | 23 | 41075579 | 41075579 | + | Missense_Mutation | SNP | G | G | C | TCGA-27-1838-01A-01D-1494-08 | TCGA-27-1838-10A-01D-1494-08 | g.chrX:41075579G>C | c.5759G>C | c.(5758-5760)tGt>tCt | p.C1920S |
GBMLGG | 23 | 41025363 | 41025363 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chrX:41025363C>T | c.2224C>T | c.(2224-2226)Cga>Tga | p.R742* |
GBMLGG | 23 | 41027339 | 41027339 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chrX:41027339G>A | c.2504G>A | c.(2503-2505)gGt>gAt | p.G835D |
GBMLGG | 23 | 41029755 | 41029755 | + | Silent | SNP | C | C | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chrX:41029755C>A | c.2910C>A | c.(2908-2910)tcC>tcA | p.S970S |
GBMLGG | 23 | 41043672 | 41043672 | + | Missense_Mutation | SNP | C | C | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chrX:41043672C>A | c.3302C>A | c.(3301-3303)cCt>cAt | p.P1101H |
GBMLGG | 23 | 41048650 | 41048650 | + | Missense_Mutation | SNP | C | C | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chrX:41048650C>A | c.3899C>A | c.(3898-3900)cCa>cAa | p.P1300Q |
GBMLGG | 23 | 41048719 | 41048719 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chrX:41048719G>A | c.3968G>A | c.(3967-3969)tGt>tAt | p.C1323Y |
GBMLGG | 23 | 41057788 | 41057788 | + | Missense_Mutation | SNP | T | T | C | TCGA-DU-6410-01A-11D-1893-08 | TCGA-DU-6410-10A-01D-1893-08 | g.chrX:41057788T>C | c.4388T>C | c.(4387-4389)aTt>aCt | p.I1463T |
GBMLGG | 23 | 41057976 | 41057976 | + | Missense_Mutation | SNP | A | A | G | TCGA-VM-A8CF-01A-11D-A36O-08 | TCGA-VM-A8CF-10A-01D-A367-08 | g.chrX:41057976A>G | c.4576A>G | c.(4576-4578)Atg>Gtg | p.M1526V |
GBMLGG | 23 | 41069807 | 41069807 | + | Missense_Mutation | SNP | A | A | C | TCGA-S9-A7QW-01A-11D-A34A-08 | TCGA-S9-A7QW-10A-01D-A34A-08 | g.chrX:41069807A>C | c.5061A>C | c.(5059-5061)ttA>ttC | p.L1687F |
GBMLGG | 23 | 41073892 | 41073892 | + | Missense_Mutation | SNP | T | T | C | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chrX:41073892T>C | c.5261T>C | c.(5260-5262)tTg>tCg | p.L1754S |
GBMLGG | 23 | 41075235 | 41075235 | + | Missense_Mutation | SNP | A | A | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chrX:41075235A>T | c.5415A>T | c.(5413-5415)gaA>gaT | p.E1805D |
GBMLGG | 23 | 41075260 | 41075260 | + | Missense_Mutation | SNP | G | G | A | TCGA-DB-A64L-01A-11D-A29Q-08 | TCGA-DB-A64L-10A-01D-A29Q-08 | g.chrX:41075260G>A | c.5440G>A | c.(5440-5442)Gat>Aat | p.D1814N |
GBMLGG | 23 | 41075424 | 41075424 | + | Silent | SNP | G | G | A | TCGA-06-5412-01A-01D-1696-08 | TCGA-06-5412-10A-01D-1696-08 | g.chrX:41075424G>A | c.5604G>A | c.(5602-5604)gtG>gtA | p.V1868V |
GBMLGG | 23 | 41075440 | 41075440 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-02-0047-01A-01D-1490-08 | TCGA-02-0047-10A-01D-1490-08 | g.chrX:41075440C>T | c.5620C>T | c.(5620-5622)Caa>Taa | p.Q1874* |
GBMLGG | 23 | 41075579 | 41075579 | + | Missense_Mutation | SNP | G | G | C | TCGA-27-1838-01A-01D-1494-08 | TCGA-27-1838-10A-01D-1494-08 | g.chrX:41075579G>C | c.5759G>C | c.(5758-5760)tGt>tCt | p.C1920S |
GBMLGG | 23 | 41084138 | 41084138 | + | Missense_Mutation | SNP | A | A | G | TCGA-DB-A4XD-01A-11D-A27K-08 | TCGA-DB-A4XD-10A-01D-A27N-08 | g.chrX:41084138A>G | c.6895A>G | c.(6895-6897)Acc>Gcc | p.T2299A |
GBMLGG | 23 | 41088882 | 41088884 | + | In_Frame_Del | DEL | AAG | AAG | - | TCGA-HW-7490-01A-11D-2024-08 | TCGA-HW-7490-10A-01D-2024-08 | g.chrX:41088882_41088884delAAG | c.7281_7283delAAG | c.(7279-7284)gaaaga>gaa | p.R2429del |
GBMLGG | 23 | 41091710 | 41091710 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chrX:41091710G>A | c.7646G>A | c.(7645-7647)gGc>gAc | p.G2549D |
HNSC | 23 | 40988323 | 40988323 | + | Missense_Mutation | SNP | C | C | T | TCGA-DQ-5625-01A-01D-1870-08 | TCGA-DQ-5625-10A-01D-1870-08 | g.chrX:40988323C>T | c.167C>T | c.(166-168)gCc>gTc | p.A56V |
HNSC | 23 | 40990715 | 40990715 | + | Missense_Mutation | SNP | G | G | T | TCGA-CV-7433-01A-11D-2129-08 | TCGA-CV-7433-10A-01D-2129-08 | g.chrX:40990715G>T | c.248G>T | c.(247-249)cGa>cTa | p.R83L |
HNSC | 23 | 40994016 | 40994016 | + | Missense_Mutation | SNP | C | C | T | TCGA-CV-A45U-01A-12D-A24D-08 | TCGA-CV-A45U-10A-01D-A24F-08 | g.chrX:40994016C>T | c.361C>T | c.(361-363)Cgt>Tgt | p.R121C |
HNSC | 23 | 41000592 | 41000592 | + | Missense_Mutation | SNP | G | G | A | TCGA-CV-6961-01A-21D-1912-08 | TCGA-CV-6961-10A-01D-1912-08 | g.chrX:41000592G>A | c.1069G>A | c.(1069-1071)Gaa>Aaa | p.E357K |
HNSC | 23 | 41000615 | 41000616 | + | Frame_Shift_Ins | INS | - | - | CACCTTA | TCGA-UP-A6WW-01A-12D-A34J-08 | TCGA-UP-A6WW-10B-01D-A34M-08 | g.chrX:41000615_41000616insCACCTTA | c.1092_1093insCACCTTA | c.(1093-1095)gtafs | p.V365fs |
HNSC | 23 | 41000616 | 41000616 | + | Missense_Mutation | SNP | G | G | T | TCGA-UP-A6WW-01A-12D-A34J-08 | TCGA-UP-A6WW-10B-01D-A34M-08 | g.chrX:41000616G>T | c.1093G>T | c.(1093-1095)Gta>Tta | p.V365L |
HNSC | 23 | 41000632 | 41000632 | + | Missense_Mutation | SNP | A | A | G | TCGA-CN-5358-01A-01D-1512-08 | TCGA-CN-5358-10A-01D-1512-08 | g.chrX:41000632A>G | c.1109A>G | c.(1108-1110)cAt>cGt | p.H370R |
HNSC | 23 | 41002598 | 41002598 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-CV-A463-01A-11D-A25Y-08 | TCGA-CV-A463-10A-01D-A25Y-08 | g.chrX:41002598C>T | c.1216C>T | c.(1216-1218)Cag>Tag | p.Q406* |
HNSC | 23 | 41007694 | 41007694 | + | Missense_Mutation | SNP | G | G | A | TCGA-BB-A5HY-01A-11D-A28R-08 | TCGA-BB-A5HY-10A-01D-A28U-08 | g.chrX:41007694G>A | c.1492G>A | c.(1492-1494)Gat>Aat | p.D498N |
HNSC | 23 | 41007737 | 41007737 | + | Missense_Mutation | SNP | G | G | T | TCGA-CN-4742-01A-02D-1512-08 | TCGA-CN-4742-10A-01D-1512-08 | g.chrX:41007737G>T | c.1535G>T | c.(1534-1536)tGg>tTg | p.W512L |
HNSC | 23 | 41027443 | 41027443 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-MT-A67F-01A-11D-A30E-08 | TCGA-MT-A67F-10A-01D-A30H-08 | g.chrX:41027443G>T | c.2608G>T | c.(2608-2610)Gag>Tag | p.E870* |
HNSC | 23 | 41027468 | 41027468 | + | Missense_Mutation | SNP | C | C | T | TCGA-CV-A468-01A-11D-A25Y-08 | TCGA-CV-A468-10A-01D-A25Y-08 | g.chrX:41027468C>T | c.2633C>T | c.(2632-2634)tCg>tTg | p.S878L |
HNSC | 23 | 41031206 | 41031206 | + | Missense_Mutation | SNP | C | C | G | TCGA-CV-7248-01A-11D-2012-08 | TCGA-CV-7248-10A-01D-2013-08 | g.chrX:41031206C>G | c.3143C>G | c.(3142-3144)cCg>cGg | p.P1048R |
HNSC | 23 | 41048594 | 41048594 | + | Silent | SNP | C | C | T | TCGA-CR-7395-01A-11D-2012-08 | TCGA-CR-7395-10A-01D-2013-08 | g.chrX:41048594C>T | c.3843C>T | c.(3841-3843)gaC>gaT | p.D1281D |
HNSC | 23 | 41056744 | 41056744 | + | Missense_Mutation | SNP | G | G | C | TCGA-T2-A6X2-01A-12D-A34J-08 | TCGA-T2-A6X2-10B-01D-A34M-08 | g.chrX:41056744G>C | c.4361G>C | c.(4360-4362)gGa>gCa | p.G1454A |
HNSC | 23 | 41060380 | 41060380 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-HD-A634-01A-11D-A28R-08 | TCGA-HD-A634-10A-01D-A28U-08 | g.chrX:41060380delG | c.4671delG | c.(4669-4671)gtgfs | p.V1557fs |
HNSC | 23 | 41069829 | 41069829 | + | Missense_Mutation | SNP | G | G | T | TCGA-CR-7374-01A-11D-2012-08 | TCGA-CR-7374-10A-01D-2013-08 | g.chrX:41069829G>T | c.5083G>T | c.(5083-5085)Gat>Tat | p.D1695Y |
HNSC | 23 | 41073879 | 41073879 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-D6-A6EK-01A-11D-A31L-08 | TCGA-D6-A6EK-10A-01D-A31J-08 | g.chrX:41073879delC | c.5248delC | c.(5248-5250)cttfs | p.L1751fs |
HNSC | 23 | 41075168 | 41075168 | + | Missense_Mutation | SNP | G | G | A | TCGA-H7-7774-01A-21D-2078-08 | TCGA-H7-7774-10A-01D-2078-08 | g.chrX:41075168G>A | c.5348G>A | c.(5347-5349)cGc>cAc | p.R1783H |
HNSC | 23 | 41075704 | 41075704 | + | Missense_Mutation | SNP | G | G | C | TCGA-CN-5369-01A-01D-1434-08 | TCGA-CN-5369-10A-01D-1434-08 | g.chrX:41075704G>C | c.5884G>C | c.(5884-5886)Gat>Cat | p.D1962H |
HNSC | 23 | 41077795 | 41077795 | + | Missense_Mutation | SNP | C | C | T | TCGA-D6-6516-01A-11D-1870-08 | TCGA-D6-6516-10A-01D-1870-08 | g.chrX:41077795C>T | c.6380C>T | c.(6379-6381)tCc>tTc | p.S2127F |
HNSC | 23 | 41077799 | 41077799 | + | Silent | SNP | G | G | A | TCGA-CQ-6224-01A-11D-1912-08 | TCGA-CQ-6224-10A-01D-1912-08 | g.chrX:41077799G>A | c.6384G>A | c.(6382-6384)ttG>ttA | p.L2128L |
HNSC | 23 | 41077827 | 41077827 | + | Missense_Mutation | SNP | G | G | A | TCGA-CR-7364-01A-11D-2012-08 | TCGA-CR-7364-10A-01D-2013-08 | g.chrX:41077827G>A | c.6412G>A | c.(6412-6414)Gcc>Acc | p.A2138T |
HNSC | 23 | 41082519 | 41082519 | + | Missense_Mutation | SNP | T | T | A | TCGA-D6-6516-01A-11D-1870-08 | TCGA-D6-6516-10A-01D-1870-08 | g.chrX:41082519T>A | c.6615T>A | c.(6613-6615)ttT>ttA | p.F2205L |
HNSC | 23 | 41088557 | 41088563 | + | Frame_Shift_Del | DEL | CACAATC | CACAATC | - | TCGA-D6-6517-01A-11D-1870-08 | TCGA-D6-6517-10A-01D-1870-08 | g.chrX:41088557_41088563delCACAATC | c.7113_7119delCACAATC | c.(7111-7119)gacacaatcfs | p.DTI2371fs |
HNSC | 23 | 41088843 | 41088843 | + | Silent | SNP | G | G | A | TCGA-IQ-A61K-01A-11D-A30E-08 | TCGA-IQ-A61K-10A-01D-A30H-08 | g.chrX:41088843G>A | c.7242G>A | c.(7240-7242)aaG>aaA | p.K2414K |
HNSC | 23 | 41088907 | 41088907 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-P3-A5QF-01A-11D-A28R-08 | TCGA-P3-A5QF-10A-01D-A28U-08 | g.chrX:41088907C>T | c.7306C>T | c.(7306-7308)Cag>Tag | p.Q2436* |
HNSC | 23 | 41088917 | 41088919 | + | In_Frame_Del | DEL | ACA | ACA | - | TCGA-IQ-7631-01A-11D-2078-08 | TCGA-IQ-7631-10A-01D-2078-08 | g.chrX:41088917_41088919delACA | c.7316_7318delACA | c.(7315-7320)tacaac>tac | p.N2441del |
HNSC | 23 | 41089764 | 41089764 | + | Missense_Mutation | SNP | A | A | G | TCGA-UF-A71D-01A-12D-A34J-08 | TCGA-UF-A71D-10B-01D-A34M-08 | g.chrX:41089764A>G | c.7490A>G | c.(7489-7491)gAc>gGc | p.D2497G |
KICH | 23 | 41002593 | 41002593 | + | Missense_Mutation | SNP | T | T | G | TCGA-KL-8323-01A-21D-2310-10 | TCGA-KL-8323-11A-01D-2310-10 | g.chrX:41002593T>G | c.1211T>G | c.(1210-1212)cTt>cGt | p.L404R |
KICH | 23 | 41010226 | 41010226 | + | Missense_Mutation | SNP | G | G | T | TCGA-KM-8477-01A-11D-2310-10 | TCGA-KM-8477-10A-01D-2311-10 | g.chrX:41010226G>T | c.1679G>T | c.(1678-1680)cGc>cTc | p.R560L |
KICH | 23 | 41029423 | 41029423 | + | Missense_Mutation | SNP | G | G | A | TCGA-KL-8331-01A-11D-2310-10 | TCGA-KL-8331-11A-01D-2310-10 | g.chrX:41029423G>A | c.2812G>A | c.(2812-2814)Ggt>Agt | p.G938S |
KICH | 23 | 41088984 | 41088985 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-KL-8334-01A-11D-2310-10 | TCGA-KL-8334-11A-01D-2310-10 | g.chrX:41088984_41088985insA | c.7383_7384insA | c.(7384-7386)agtfs | p.S2462fs |
KICH | 23 | 41088985 | 41088986 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-KL-8334-01A-11D-2310-10 | TCGA-KL-8334-11A-01D-2310-10 | g.chrX:41088985_41088986insA | c.7384_7385insA | c.(7384-7386)agtfs | p.S2462fs |
KIPAN | 23 | 40999924 | 40999924 | + | Missense_Mutation | SNP | C | C | A | TCGA-B9-5156-01A-01D-1589-08 | TCGA-B9-5156-10A-01D-1589-08 | g.chrX:40999924C>A | c.670C>A | c.(670-672)Ctt>Att | p.L224I |
KIPAN | 23 | 41002593 | 41002593 | + | Missense_Mutation | SNP | T | T | G | TCGA-KL-8323-01A-21D-2310-10 | TCGA-KL-8323-11A-01D-2310-10 | g.chrX:41002593T>G | c.1211T>G | c.(1210-1212)cTt>cGt | p.L404R |
KIPAN | 23 | 41010226 | 41010226 | + | Missense_Mutation | SNP | G | G | T | TCGA-KM-8477-01A-11D-2310-10 | TCGA-KM-8477-10A-01D-2311-10 | g.chrX:41010226G>T | c.1679G>T | c.(1678-1680)cGc>cTc | p.R560L |
KIPAN | 23 | 41025293 | 41025293 | + | Missense_Mutation | SNP | C | C | A | TCGA-CJ-4875-01A-01D-1373-10 | TCGA-CJ-4875-11A-01D-1373-10 | g.chrX:41025293C>A | c.2154C>A | c.(2152-2154)gaC>gaA | p.D718E |
KIPAN | 23 | 41025335 | 41025335 | + | Silent | SNP | A | A | G | TCGA-CZ-4861-01A-01D-1373-10 | TCGA-CZ-4861-11A-01D-1373-10 | g.chrX:41025335A>G | c.2196A>G | c.(2194-2196)ttA>ttG | p.L732L |
KIPAN | 23 | 41029423 | 41029423 | + | Missense_Mutation | SNP | G | G | A | TCGA-KL-8331-01A-11D-2310-10 | TCGA-KL-8331-11A-01D-2310-10 | g.chrX:41029423G>A | c.2812G>A | c.(2812-2814)Ggt>Agt | p.G938S |
KIPAN | 23 | 41043810 | 41043810 | + | Missense_Mutation | SNP | C | C | T | TCGA-B9-A69E-01A-11D-A31X-10 | TCGA-B9-A69E-10A-01D-A31X-10 | g.chrX:41043810C>T | c.3440C>T | c.(3439-3441)gCc>gTc | p.A1147V |
KIPAN | 23 | 41047253 | 41047253 | + | Silent | SNP | A | A | G | TCGA-BP-4160-01A-02D-1366-10 | TCGA-BP-4160-11A-01D-1806-10 | g.chrX:41047253A>G | c.3693A>G | c.(3691-3693)agA>agG | p.R1231R |
KIPAN | 23 | 41077774 | 41077774 | + | Missense_Mutation | SNP | T | T | C | TCGA-CJ-4881-01A-01D-1373-10 | TCGA-CJ-4881-11A-01D-1373-10 | g.chrX:41077774T>C | c.6359T>C | c.(6358-6360)aTa>aCa | p.I2120T |
KIPAN | 23 | 41088595 | 41088595 | + | Missense_Mutation | SNP | C | C | A | TCGA-BP-5168-01A-01D-1421-08 | TCGA-BP-5168-11A-01D-1421-08 | g.chrX:41088595C>A | c.7151C>A | c.(7150-7152)gCa>gAa | p.A2384E |
KIPAN | 23 | 41088984 | 41088985 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-KL-8334-01A-11D-2310-10 | TCGA-KL-8334-11A-01D-2310-10 | g.chrX:41088984_41088985insA | c.7383_7384insA | c.(7384-7386)agtfs | p.S2462fs |
KIPAN | 23 | 41088985 | 41088986 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-KL-8334-01A-11D-2310-10 | TCGA-KL-8334-11A-01D-2310-10 | g.chrX:41088985_41088986insA | c.7384_7385insA | c.(7384-7386)agtfs | p.S2462fs |
KIPAN | 23 | 41091721 | 41091721 | + | Missense_Mutation | SNP | C | C | G | TCGA-A3-3370-01A-02D-1421-08 | TCGA-A3-3370-11A-01D-1421-08 | g.chrX:41091721C>G | c.7657C>G | c.(7657-7659)Caa>Gaa | p.Q2553E |
KIRC | 23 | 41025293 | 41025293 | + | Missense_Mutation | SNP | C | C | A | TCGA-CJ-4875-01A-01D-1373-10 | TCGA-CJ-4875-11A-01D-1373-10 | g.chrX:41025293C>A | c.2154C>A | c.(2152-2154)gaC>gaA | p.D718E |
KIRC | 23 | 41025335 | 41025335 | + | Silent | SNP | A | A | G | TCGA-CZ-4861-01A-01D-1373-10 | TCGA-CZ-4861-11A-01D-1373-10 | g.chrX:41025335A>G | c.2196A>G | c.(2194-2196)ttA>ttG | p.L732L |
KIRC | 23 | 41047253 | 41047253 | + | Silent | SNP | A | A | G | TCGA-BP-4160-01A-02D-1366-10 | TCGA-BP-4160-11A-01D-1806-10 | g.chrX:41047253A>G | c.3693A>G | c.(3691-3693)agA>agG | p.R1231R |
KIRC | 23 | 41077774 | 41077774 | + | Missense_Mutation | SNP | T | T | C | TCGA-CJ-4881-01A-01D-1373-10 | TCGA-CJ-4881-11A-01D-1373-10 | g.chrX:41077774T>C | c.6359T>C | c.(6358-6360)aTa>aCa | p.I2120T |
KIRC | 23 | 41088595 | 41088595 | + | Missense_Mutation | SNP | C | C | A | TCGA-BP-5168-01A-01D-1421-08 | TCGA-BP-5168-11A-01D-1421-08 | g.chrX:41088595C>A | c.7151C>A | c.(7150-7152)gCa>gAa | p.A2384E |
KIRC | 23 | 41091721 | 41091721 | + | Missense_Mutation | SNP | C | C | G | TCGA-A3-3370-01A-02D-1421-08 | TCGA-A3-3370-11A-01D-1421-08 | g.chrX:41091721C>G | c.7657C>G | c.(7657-7659)Caa>Gaa | p.Q2553E |
KIRP | 23 | 40999924 | 40999924 | + | Missense_Mutation | SNP | C | C | A | TCGA-B9-5156-01A-01D-1589-08 | TCGA-B9-5156-10A-01D-1589-08 | g.chrX:40999924C>A | c.670C>A | c.(670-672)Ctt>Att | p.L224I |
KIRP | 23 | 41043810 | 41043810 | + | Missense_Mutation | SNP | C | C | T | TCGA-B9-A69E-01A-11D-A31X-10 | TCGA-B9-A69E-10A-01D-A31X-10 | g.chrX:41043810C>T | c.3440C>T | c.(3439-3441)gCc>gTc | p.A1147V |
LAML | 23 | 41010296 | 41010296 | + | Silent | SNP | G | G | A | TCGA-AB-3001-03A-01D-0739-09 | TCGA-AB-3001-11A-01D-0739-09 | g.chrX:41010296G>A | c.1749G>A | c.(1747-1749)gcG>gcA | p.A583A |
LAML | 23 | 41027390 | 41027391 | + | Frame_Shift_Ins | INS | - | - | CG | TCGA-AB-2934-03A-01W-0755-09 | TCGA-AB-2934-11A-01W-0755-09 | g.chrX:41027390_41027391insCG | c.2555_2556insCG | c.(2554-2559)cgagtafs | p.V853fs |
LGG | 23 | 41025363 | 41025363 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chrX:41025363C>T | c.2224C>T | c.(2224-2226)Cga>Tga | p.R742* |
LGG | 23 | 41027339 | 41027339 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chrX:41027339G>A | c.2504G>A | c.(2503-2505)gGt>gAt | p.G835D |
LGG | 23 | 41029755 | 41029755 | + | Silent | SNP | C | C | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chrX:41029755C>A | c.2910C>A | c.(2908-2910)tcC>tcA | p.S970S |
LGG | 23 | 41043672 | 41043672 | + | Missense_Mutation | SNP | C | C | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chrX:41043672C>A | c.3302C>A | c.(3301-3303)cCt>cAt | p.P1101H |
LGG | 23 | 41048650 | 41048650 | + | Missense_Mutation | SNP | C | C | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chrX:41048650C>A | c.3899C>A | c.(3898-3900)cCa>cAa | p.P1300Q |
LGG | 23 | 41048719 | 41048719 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chrX:41048719G>A | c.3968G>A | c.(3967-3969)tGt>tAt | p.C1323Y |
LGG | 23 | 41057788 | 41057788 | + | Missense_Mutation | SNP | T | T | C | TCGA-DU-6410-01A-11D-1893-08 | TCGA-DU-6410-10A-01D-1893-08 | g.chrX:41057788T>C | c.4388T>C | c.(4387-4389)aTt>aCt | p.I1463T |
LGG | 23 | 41057976 | 41057976 | + | Missense_Mutation | SNP | A | A | G | TCGA-VM-A8CF-01A-11D-A36O-08 | TCGA-VM-A8CF-10A-01D-A367-08 | g.chrX:41057976A>G | c.4576A>G | c.(4576-4578)Atg>Gtg | p.M1526V |
LGG | 23 | 41069807 | 41069807 | + | Missense_Mutation | SNP | A | A | C | TCGA-S9-A7QW-01A-11D-A34A-08 | TCGA-S9-A7QW-10A-01D-A34A-08 | g.chrX:41069807A>C | c.5061A>C | c.(5059-5061)ttA>ttC | p.L1687F |
LGG | 23 | 41073892 | 41073892 | + | Missense_Mutation | SNP | T | T | C | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chrX:41073892T>C | c.5261T>C | c.(5260-5262)tTg>tCg | p.L1754S |
LGG | 23 | 41075235 | 41075235 | + | Missense_Mutation | SNP | A | A | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chrX:41075235A>T | c.5415A>T | c.(5413-5415)gaA>gaT | p.E1805D |
LGG | 23 | 41075260 | 41075260 | + | Missense_Mutation | SNP | G | G | A | TCGA-DB-A64L-01A-11D-A29Q-08 | TCGA-DB-A64L-10A-01D-A29Q-08 | g.chrX:41075260G>A | c.5440G>A | c.(5440-5442)Gat>Aat | p.D1814N |
LGG | 23 | 41084138 | 41084138 | + | Missense_Mutation | SNP | A | A | G | TCGA-DB-A4XD-01A-11D-A27K-08 | TCGA-DB-A4XD-10A-01D-A27N-08 | g.chrX:41084138A>G | c.6895A>G | c.(6895-6897)Acc>Gcc | p.T2299A |
LGG | 23 | 41088882 | 41088884 | + | In_Frame_Del | DEL | AAG | AAG | - | TCGA-HW-7490-01A-11D-2024-08 | TCGA-HW-7490-10A-01D-2024-08 | g.chrX:41088882_41088884delAAG | c.7281_7283delAAG | c.(7279-7284)gaaaga>gaa | p.R2429del |
LGG | 23 | 41091710 | 41091710 | + | Missense_Mutation | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chrX:41091710G>A | c.7646G>A | c.(7645-7647)gGc>gAc | p.G2549D |
LIHC | 23 | 41002598 | 41002598 | + | Missense_Mutation | SNP | C | C | G | TCGA-MI-A75C-01A-11D-A32G-10 | TCGA-MI-A75C-10A-01D-A32G-10 | g.chrX:41002598C>G | c.1216C>G | c.(1216-1218)Cag>Gag | p.Q406E |
LIHC | 23 | 41022048 | 41022048 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-ZS-A9CE-01A-11D-A36X-10 | TCGA-ZS-A9CE-10A-01D-A370-10 | g.chrX:41022048G>T | c.1903G>T | c.(1903-1905)Gaa>Taa | p.E635* |
LIHC | 23 | 41043827 | 41043827 | + | Frame_Shift_Del | DEL | A | A | - | TCGA-G3-A3CJ-01A-11D-A20W-10 | TCGA-G3-A3CJ-10A-01D-A20W-10 | g.chrX:41043827delA | c.3457delA | c.(3457-3459)aaafs | p.K1153fs |
LIHC | 23 | 41048571 | 41048571 | + | Missense_Mutation | SNP | G | G | A | TCGA-DD-AACD-01A-11D-A40R-10 | TCGA-DD-AACD-10A-01D-A40U-10 | g.chrX:41048571G>A | c.3820G>A | c.(3820-3822)Ggc>Agc | p.G1274S |
LIHC | 23 | 41069765 | 41069765 | + | Silent | SNP | T | T | A | TCGA-UB-A7ME-01A-11D-A33K-10 | TCGA-UB-A7ME-10A-01D-A33K-10 | g.chrX:41069765T>A | c.5019T>A | c.(5017-5019)ctT>ctA | p.L1673L |
LIHC | 23 | 41069767 | 41069767 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-DD-A39Y-01A-11D-A20W-10 | TCGA-DD-A39Y-11A-11D-A20W-10 | g.chrX:41069767delG | c.5021delG | c.(5020-5022)tggfs | p.W1674fs |
LIHC | 23 | 41069811 | 41069811 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-DD-A1EG-01A-11D-A20W-10 | TCGA-DD-A1EG-10A-01D-A20W-10 | g.chrX:41069811delT | c.5065delT | c.(5065-5067)tttfs | p.F1690fs |
LIHC | 23 | 41075386 | 41075386 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-DD-AADE-01A-11D-A40R-10 | TCGA-DD-AADE-10A-01D-A40U-10 | g.chrX:41075386G>T | c.5566G>T | c.(5566-5568)Gag>Tag | p.E1856* |
LIHC | 23 | 41075804 | 41075804 | + | Missense_Mutation | SNP | A | A | G | TCGA-DD-A39Y-01A-11D-A20W-10 | TCGA-DD-A39Y-11A-11D-A20W-10 | g.chrX:41075804A>G | c.5984A>G | c.(5983-5985)aAc>aGc | p.N1995S |
LIHC | 23 | 41088999 | 41088999 | + | Silent | SNP | A | A | G | TCGA-CC-A3MA-01A-11D-A20W-10 | TCGA-CC-A3MA-10A-01D-A20W-10 | g.chrX:41088999A>G | c.7398A>G | c.(7396-7398)acA>acG | p.T2466T |
LUAD | 23 | 40994008 | 40994008 | + | Missense_Mutation | SNP | G | G | A | TCGA-69-7979-01A-11D-2184-08 | TCGA-69-7979-10A-01D-2184-08 | g.chrX:40994008G>A | c.353G>A | c.(352-354)cGa>cAa | p.R118Q |
LUAD | 23 | 40999908 | 40999908 | + | Splice_Site | SNP | G | G | C | TCGA-L9-A443-01A-12D-A24D-08 | TCGA-L9-A443-10A-01D-A24F-08 | g.chrX:40999908G>C | | c.e7-1 | |
LUAD | 23 | 41000347 | 41000347 | + | Missense_Mutation | SNP | A | A | G | TCGA-55-1592-01A-01D-0969-08 | TCGA-55-1592-11A-01D-0969-08 | g.chrX:41000347A>G | c.899A>G | c.(898-900)aAt>aGt | p.N300S |
LUAD | 23 | 41000658 | 41000658 | + | Missense_Mutation | SNP | G | G | C | TCGA-64-5781-01A-01D-1625-08 | TCGA-64-5781-10A-01D-1625-08 | g.chrX:41000658G>C | c.1135G>C | c.(1135-1137)Gag>Cag | p.E379Q |
LUAD | 23 | 41010268 | 41010268 | + | Missense_Mutation | SNP | G | G | C | TCGA-NJ-A4YF-01A-12D-A25L-08 | TCGA-NJ-A4YF-10A-01D-A25L-08 | g.chrX:41010268G>C | c.1721G>C | c.(1720-1722)aGa>aCa | p.R574T |
LUAD | 23 | 41012324 | 41012324 | + | Silent | SNP | A | A | G | TCGA-05-4430-01A-02D-1265-08 | TCGA-05-4430-10A-01D-1265-08 | g.chrX:41012324A>G | c.1887A>G | c.(1885-1887)ctA>ctG | p.L629L |
LUAD | 23 | 41025388 | 41025388 | + | Missense_Mutation | SNP | G | G | A | TCGA-38-4630-01A-01D-1265-08 | TCGA-38-4630-11A-01D-1265-08 | g.chrX:41025388G>A | c.2249G>A | c.(2248-2250)cGa>cAa | p.R750Q |
LUAD | 23 | 41025463 | 41025463 | + | Missense_Mutation | SNP | G | G | T | TCGA-05-4396-01A-21D-1855-08 | TCGA-05-4396-10A-01D-1855-08 | g.chrX:41025463G>T | c.2324G>T | c.(2323-2325)tGg>tTg | p.W775L |
LUAD | 23 | 41029419 | 41029419 | + | Silent | SNP | G | G | T | TCGA-86-A456-01A-11D-A24D-08 | TCGA-86-A456-10A-01D-A24F-08 | g.chrX:41029419G>T | c.2808G>T | c.(2806-2808)gtG>gtT | p.V936V |
LUAD | 23 | 41029762 | 41029762 | + | Missense_Mutation | SNP | C | C | T | TCGA-44-6147-01A-11D-1753-08 | TCGA-44-6147-10A-01D-1753-08 | g.chrX:41029762C>T | c.2917C>T | c.(2917-2919)Cct>Tct | p.P973S |
LUAD | 23 | 41043333 | 41043333 | + | Missense_Mutation | SNP | C | C | A | TCGA-69-A59K-01A-11D-A25L-08 | TCGA-69-A59K-10A-01D-A25L-08 | g.chrX:41043333C>A | c.3231C>A | c.(3229-3231)gaC>gaA | p.D1077E |
LUAD | 23 | 41043661 | 41043661 | + | Silent | SNP | C | C | T | TCGA-44-2656-01A-02D-0969-08 | TCGA-44-2656-10A-01D-0969-08 | g.chrX:41043661C>T | c.3291C>T | c.(3289-3291)gcC>gcT | p.A1097A |
LUAD | 23 | 41055512 | 41055512 | + | Missense_Mutation | SNP | G | G | A | TCGA-71-8520-01A-11D-2393-08 | TCGA-71-8520-10A-01D-2393-08 | g.chrX:41055512G>A | c.3986G>A | c.(3985-3987)cGt>cAt | p.R1329H |
LUAD | 23 | 41055569 | 41055569 | + | Missense_Mutation | SNP | G | G | T | TCGA-17-Z055-01A-01W-0747-08 | TCGA-17-Z055-11A-01W-0747-08 | g.chrX:41055569G>T | c.4043G>T | c.(4042-4044)cGg>cTg | p.R1348L |
LUAD | 23 | 41056749 | 41056749 | + | Missense_Mutation | SNP | G | G | A | TCGA-MP-A4TH-01A-31D-A25L-08 | TCGA-MP-A4TH-10A-01D-A25L-08 | g.chrX:41056749G>A | c.4366G>A | c.(4366-4368)Gct>Act | p.A1456T |
LUAD | 23 | 41057842 | 41057842 | + | Missense_Mutation | SNP | G | G | T | TCGA-17-Z022-01A-01W-0746-08 | TCGA-17-Z022-11A-01W-0746-08 | g.chrX:41057842G>T | c.4442G>T | c.(4441-4443)gGa>gTa | p.G1481V |
LUAD | 23 | 41069770 | 41069770 | + | Missense_Mutation | SNP | G | G | T | TCGA-55-8620-01A-11D-2393-08 | TCGA-55-8620-10A-01D-2393-08 | g.chrX:41069770G>T | c.5024G>T | c.(5023-5025)gGt>gTt | p.G1675V |
LUAD | 23 | 41073863 | 41073863 | + | Silent | SNP | T | T | A | TCGA-44-3919-01A-02D-1458-08 | TCGA-44-3919-10A-01D-1458-08 | g.chrX:41073863T>A | c.5232T>A | c.(5230-5232)atT>atA | p.I1744I |
LUAD | 23 | 41075524 | 41075524 | + | Missense_Mutation | SNP | G | G | A | TCGA-17-Z023-01A-01W-0746-08 | TCGA-17-Z023-11A-01W-0746-08 | g.chrX:41075524G>A | c.5704G>A | c.(5704-5706)Gat>Aat | p.D1902N |
LUAD | 23 | 41075556 | 41075556 | + | Silent | SNP | T | T | C | TCGA-86-A456-01A-11D-A24D-08 | TCGA-86-A456-10A-01D-A24F-08 | g.chrX:41075556T>C | c.5736T>C | c.(5734-5736)gaT>gaC | p.D1912D |
LUAD | 23 | 41075707 | 41075707 | + | Missense_Mutation | SNP | G | G | C | TCGA-17-Z057-01A-01W-0747-08 | TCGA-17-Z057-11A-01W-0747-08 | g.chrX:41075707G>C | c.5887G>C | c.(5887-5889)Gat>Cat | p.D1963H |
LUAD | 23 | 41075817 | 41075817 | + | Missense_Mutation | SNP | G | G | A | TCGA-05-4427-01A-21D-1855-08 | TCGA-05-4427-10A-01D-1855-08 | g.chrX:41075817G>A | c.5997G>A | c.(5995-5997)atG>atA | p.M1999I |
LUAD | 23 | 41077680 | 41077680 | + | Missense_Mutation | SNP | G | G | T | TCGA-69-7763-01A-11D-2167-08 | TCGA-69-7763-10A-01D-2167-08 | g.chrX:41077680G>T | c.6265G>T | c.(6265-6267)Gct>Tct | p.A2089S |
LUAD | 23 | 41082625 | 41082625 | + | Missense_Mutation | SNP | G | G | T | TCGA-50-5930-01A-11D-1753-08 | TCGA-50-5930-11A-01D-1753-08 | g.chrX:41082625G>T | c.6721G>T | c.(6721-6723)Gtc>Ttc | p.V2241F |
LUAD | 23 | 41084348 | 41084348 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-69-7978-01A-11D-2184-08 | TCGA-69-7978-10A-01D-2184-08 | g.chrX:41084348delT | c.7019delT | c.(7018-7020)cttfs | p.L2341fs |
LUAD | 23 | 41088852 | 41088852 | + | Missense_Mutation | SNP | G | G | T | TCGA-91-6831-01A-11D-1855-08 | TCGA-91-6831-11A-02D-1855-08 | g.chrX:41088852G>T | c.7251G>T | c.(7249-7251)tgG>tgT | p.W2417C |
LUAD | 23 | 41088907 | 41088907 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-50-6594-01A-11D-1753-08 | TCGA-50-6594-11A-01D-1753-08 | g.chrX:41088907C>T | c.7306C>T | c.(7306-7308)Cag>Tag | p.Q2436* |
LUAD | 23 | 41089775 | 41089775 | + | Missense_Mutation | SNP | C | C | A | TCGA-55-7911-01A-11D-2167-08 | TCGA-55-7911-10A-01D-2167-08 | g.chrX:41089775C>A | c.7501C>A | c.(7501-7503)Cca>Aca | p.P2501T |
LUAD | 23 | 41091776 | 41091776 | + | Silent | SNP | G | G | A | TCGA-MN-A4N4-01A-12D-A24P-08 | TCGA-MN-A4N4-10A-01D-A24P-08 | g.chrX:41091776G>A | c.7712G>A | c.(7711-7713)tGa>tAa | p.*2571* |
LUSC | 23 | 40994071 | 40994071 | + | Missense_Mutation | SNP | G | G | T | TCGA-66-2734-01A-01D-0983-08 | TCGA-66-2734-11A-01D-0983-08 | g.chrX:40994071G>T | c.416G>T | c.(415-417)gGc>gTc | p.G139V |
LUSC | 23 | 41000371 | 41000371 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-66-2763-01A-01D-1522-08 | TCGA-66-2763-11A-01D-1522-08 | g.chrX:41000371C>A | c.923C>A | c.(922-924)tCa>tAa | p.S308* |
LUSC | 23 | 41010252 | 41010252 | + | Missense_Mutation | SNP | G | G | C | TCGA-43-5668-01A-01D-1632-08 | TCGA-43-5668-11A-01D-1632-08 | g.chrX:41010252G>C | c.1705G>C | c.(1705-1707)Gca>Cca | p.A569P |
LUSC | 23 | 41026799 | 41026799 | + | Missense_Mutation | SNP | C | C | T | TCGA-66-2787-01A-01D-0983-08 | TCGA-66-2787-11A-01D-0983-08 | g.chrX:41026799C>T | c.2393C>T | c.(2392-2394)aCg>aTg | p.T798M |
LUSC | 23 | 41056655 | 41056655 | + | Missense_Mutation | SNP | G | G | C | TCGA-34-5929-01A-11D-1817-08 | TCGA-34-5929-11A-01D-1817-08 | g.chrX:41056655G>C | c.4272G>C | c.(4270-4272)gaG>gaC | p.E1424D |
LUSC | 23 | 41064718 | 41064718 | + | Missense_Mutation | SNP | G | G | C | TCGA-34-5929-01A-11D-1817-08 | TCGA-34-5929-11A-01D-1817-08 | g.chrX:41064718G>C | c.4987G>C | c.(4987-4989)Gtg>Ctg | p.V1663L |
LUSC | 23 | 41075504 | 41075505 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-66-2759-01A-01D-1522-08 | TCGA-66-2759-11A-01D-1522-08 | g.chrX:41075504_41075505insT | c.5684_5685insT | c.(5683-5688)aatcgcfs | p.R1896fs |
LUSC | 23 | 41075634 | 41075635 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-66-2768-01A-01D-1522-08 | TCGA-66-2768-11A-01D-1522-08 | g.chrX:41075634_41075635insT | c.5814_5815insT | c.(5815-5817)tacfs | p.Y1939fs |
LUSC | 23 | 41075775 | 41075775 | + | Silent | SNP | A | A | T | TCGA-66-2786-01A-01D-1522-08 | TCGA-66-2786-11A-01D-1522-08 | g.chrX:41075775A>T | c.5955A>T | c.(5953-5955)tcA>tcT | p.S1985S |
LUSC | 23 | 41078486 | 41078486 | + | Splice_Site | SNP | T | T | A | TCGA-39-5024-01A-21D-1817-08 | TCGA-39-5024-11A-01D-1817-08 | g.chrX:41078486T>A | | c.e38+2 | |
OV | 23 | 40988342 | 40988342 | + | Missense_Mutation | SNP | T | T | A | TCGA-13-2071-01A-02D-1526-09 | TCGA-13-2071-10A-01D-1526-09 | g.chrX:40988342T>A | c.186T>A | c.(184-186)gaT>gaA | p.D62E |
OV | 23 | 40990733 | 40990733 | + | Missense_Mutation | SNP | T | T | G | TCGA-61-1727-01A-01W-0639-09 | TCGA-61-1727-11A-01W-0639-09 | g.chrX:40990733T>G | c.266T>G | c.(265-267)tTg>tGg | p.L89W |
OV | 23 | 41000577 | 41000577 | + | Missense_Mutation | SNP | A | A | G | TCGA-61-1900-01A-01W-0639-09 | TCGA-61-1900-11A-01W-0640-09 | g.chrX:41000577A>G | c.1054A>G | c.(1054-1056)Atg>Gtg | p.M352V |
OV | 23 | 41075555 | 41075555 | + | Missense_Mutation | SNP | A | A | G | TCGA-61-1995-01A-01W-0722-08 | TCGA-61-1995-11A-01W-0722-08 | g.chrX:41075555A>G | c.5735A>G | c.(5734-5736)gAt>gGt | p.D1912G |
PAAD | 23 | 41000309 | 41000309 | + | Silent | SNP | A | A | G | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chrX:41000309A>G | c.861A>G | c.(859-861)gaA>gaG | p.E287E |
PAAD | 23 | 41029282 | 41029282 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-XD-AAUI-01A-42D-A40W-08 | TCGA-XD-AAUI-10A-01D-A40W-08 | g.chrX:41029282C>T | c.2671C>T | c.(2671-2673)Cga>Tga | p.R891* |
PAAD | 23 | 41031200 | 41031200 | + | Missense_Mutation | SNP | T | T | G | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chrX:41031200T>G | c.3137T>G | c.(3136-3138)cTt>cGt | p.L1046R |
PAAD | 23 | 41045841 | 41045841 | + | Silent | SNP | C | C | A | TCGA-HZ-A77Q-01A-11D-A36O-08 | TCGA-HZ-A77Q-10A-01D-A367-08 | g.chrX:41045841C>A | c.3630C>A | c.(3628-3630)tcC>tcA | p.S1210S |
PAAD | 23 | 41075627 | 41075627 | + | Missense_Mutation | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chrX:41075627G>A | c.5807G>A | c.(5806-5808)cGt>cAt | p.R1936H |
PCPG | 23 | 40990708 | 40990708 | + | Splice_Site | SNP | A | A | G | TCGA-WB-A818-01A-11D-A35I-08 | TCGA-WB-A818-10A-01D-A35G-08 | g.chrX:40990708A>G | | c.e4-1 | |
PCPG | 23 | 41012243 | 41012246 | + | Frame_Shift_Del | DEL | AATC | AATC | - | TCGA-QR-A70U-01A-11D-A35D-08 | TCGA-QR-A70U-10A-01D-A35B-08 | g.chrX:41012243_41012246delAATC | c.1806_1809delAATC | c.(1804-1809)ttaatcfs | p.LI602fs |
PCPG | 23 | 41045776 | 41045776 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-QR-A70U-01A-11D-A35D-08 | TCGA-QR-A70U-10A-01D-A35B-08 | g.chrX:41045776C>T | c.3565C>T | c.(3565-3567)Caa>Taa | p.Q1189* |
PCPG | 23 | 41069761 | 41069761 | + | Splice_Site | SNP | G | G | A | TCGA-QR-A70U-01A-11D-A35D-08 | TCGA-QR-A70U-10A-01D-A35B-08 | g.chrX:41069761G>A | | c.e33-1 | |
PRAD | 23 | 40988337 | 40988337 | + | Nonsense_Mutation | SNP | G | G | T | TCGA-ZG-A9LU-01A-11D-A41K-08 | TCGA-ZG-A9LU-10A-01D-A41N-08 | g.chrX:40988337G>T | c.181G>T | c.(181-183)Gaa>Taa | p.E61* |
PRAD | 23 | 40999970 | 40999970 | + | Missense_Mutation | SNP | A | A | G | TCGA-HC-8257-01A-11D-2260-08 | TCGA-HC-8257-10A-01D-2260-08 | g.chrX:40999970A>G | c.716A>G | c.(715-717)gAt>gGt | p.D239G |
PRAD | 23 | 41000651 | 41000651 | + | Silent | SNP | G | G | A | TCGA-EJ-5517-01A-01D-1576-08 | TCGA-EJ-5517-10A-01D-1577-08 | g.chrX:41000651G>A | c.1128G>A | c.(1126-1128)gaG>gaA | p.E376E |
PRAD | 23 | 41029390 | 41029390 | + | Missense_Mutation | SNP | G | G | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chrX:41029390G>A | c.2779G>A | c.(2779-2781)Gta>Ata | p.V927I |
PRAD | 23 | 41075904 | 41075904 | + | Splice_Site | SNP | C | C | T | TCGA-V1-A9ZG-01A-11D-A41K-08 | TCGA-V1-A9ZG-10A-01D-A41N-08 | g.chrX:41075904C>T | c.6084C>T | c.(6082-6084)ccC>ccT | p.P2028P |
PRAD | 23 | 41082490 | 41082490 | + | Missense_Mutation | SNP | C | C | T | TCGA-YL-A8SL-01B-21D-A377-08 | TCGA-YL-A8SL-10A-01D-A37A-08 | g.chrX:41082490C>T | c.6586C>T | c.(6586-6588)Ctt>Ttt | p.L2196F |
READ | 23 | 40996156 | 40996156 | + | Missense_Mutation | SNP | A | A | C | TCGA-AG-3892-01A-01W-1073-09 | TCGA-AG-3892-10A-01W-1073-09 | g.chrX:40996156A>C | c.535A>C | c.(535-537)Aat>Cat | p.N179H |
READ | 23 | 41007672 | 41007672 | + | Silent | SNP | G | G | A | TCGA-AG-A026-01A-32W-A096-10 | TCGA-AG-A026-10A-01W-A096-10 | g.chrX:41007672G>A | c.1470G>A | c.(1468-1470)ctG>ctA | p.L490L |
READ | 23 | 41084340 | 41084340 | + | Missense_Mutation | SNP | G | G | T | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chrX:41084340G>T | c.7011G>T | c.(7009-7011)ttG>ttT | p.L2337F |
SKCM | 23 | 40982966 | 40982966 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-EE-A3J7-06A-11D-A20D-08 | TCGA-EE-A3J7-10A-01D-A20D-08 | g.chrX:40982966C>T | c.85C>T | c.(85-87)Caa>Taa | p.Q29* |
SKCM | 23 | 40982969 | 40982969 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-ER-A198-06A-11D-A196-08 | TCGA-ER-A198-10A-01D-A198-08 | g.chrX:40982969C>T | c.88C>T | c.(88-90)Cag>Tag | p.Q30* |
SKCM | 23 | 41000634 | 41000634 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-D9-A148-06A-11D-A19A-08 | TCGA-D9-A148-10A-01D-A19A-08 | g.chrX:41000634C>T | c.1111C>T | c.(1111-1113)Cga>Tga | p.R371* |
SKCM | 23 | 41007791 | 41007791 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3AF-06A-11D-A196-08 | TCGA-EE-A3AF-10A-01D-A198-08 | g.chrX:41007791G>A | c.1589G>A | c.(1588-1590)aGt>aAt | p.S530N |
SKCM | 23 | 41010280 | 41010283 | + | Frame_Shift_Del | DEL | GTTT | GTTT | - | TCGA-ER-A2NH-06A-11D-A196-08 | TCGA-ER-A2NH-10A-01D-A198-08 | g.chrX:41010280_41010283delGTTT | c.1733_1736delGTTT | c.(1732-1737)agtttgfs | p.SL578fs |
SKCM | 23 | 41029282 | 41029282 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chrX:41029282C>T | c.2671C>T | c.(2671-2673)Cga>Tga | p.R891* |
SKCM | 23 | 41029487 | 41029487 | + | Splice_Site | SNP | C | C | T | TCGA-EE-A2MF-06A-11D-A21A-08 | TCGA-EE-A2MF-10B-01D-A21A-08 | g.chrX:41029487C>T | c.2876C>T | c.(2875-2877)tCg>tTg | p.S959L |
SKCM | 23 | 41043842 | 41043842 | + | Silent | SNP | T | T | C | TCGA-EB-A5UL-06A-11D-A30X-08 | TCGA-EB-A5UL-10A-01D-A30X-08 | g.chrX:41043842T>C | c.3472T>C | c.(3472-3474)Ttg>Ctg | p.L1158L |
SKCM | 23 | 41043859 | 41043859 | + | Silent | SNP | C | C | T | TCGA-D3-A51G-06A-11D-A25O-08 | TCGA-D3-A51G-10A-01D-A25O-08 | g.chrX:41043859C>T | c.3489C>T | c.(3487-3489)ggC>ggT | p.G1163G |
SKCM | 23 | 41045827 | 41045827 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A51G-06A-11D-A25O-08 | TCGA-D3-A51G-10A-01D-A25O-08 | g.chrX:41045827C>T | c.3616C>T | c.(3616-3618)Cct>Tct | p.P1206S |
SKCM | 23 | 41048638 | 41048638 | + | Missense_Mutation | SNP | T | T | C | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chrX:41048638T>C | c.3887T>C | c.(3886-3888)tTt>tCt | p.F1296S |
SKCM | 23 | 41055511 | 41055511 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chrX:41055511C>T | c.3985C>T | c.(3985-3987)Cgt>Tgt | p.R1329C |
SKCM | 23 | 41055511 | 41055511 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chrX:41055511C>T | c.3985C>T | c.(3985-3987)Cgt>Tgt | p.R1329C |
SKCM | 23 | 41055568 | 41055568 | + | Missense_Mutation | SNP | C | C | G | TCGA-ER-A19P-06A-11D-A196-08 | TCGA-ER-A19P-10A-01D-A198-08 | g.chrX:41055568C>G | c.4042C>G | c.(4042-4044)Cgg>Ggg | p.R1348G |
SKCM | 23 | 41055614 | 41055614 | + | Splice_Site | SNP | T | T | G | TCGA-FS-A1Z0-06A-11D-A197-08 | TCGA-FS-A1Z0-10A-01D-A199-08 | g.chrX:41055614T>G | | c.e27+2 | |
SKCM | 23 | 41057871 | 41057871 | + | Missense_Mutation | SNP | G | G | A | TCGA-FS-A1Z0-06A-11D-A197-08 | TCGA-FS-A1Z0-10A-01D-A199-08 | g.chrX:41057871G>A | c.4471G>A | c.(4471-4473)Gtc>Atc | p.V1491I |
SKCM | 23 | 41069763 | 41069763 | + | Splice_Site | SNP | C | C | T | TCGA-ER-A42L-06A-11D-A24R-08 | TCGA-ER-A42L-10A-01D-A24R-08 | g.chrX:41069763C>T | c.5017C>T | c.(5017-5019)Ctt>Ttt | p.L1673F |
SKCM | 23 | 41069821 | 41069821 | + | Missense_Mutation | SNP | C | C | T | TCGA-DA-A1HV-06A-21D-A196-08 | TCGA-DA-A1HV-10A-01D-A198-08 | g.chrX:41069821C>T | c.5075C>T | c.(5074-5076)tCa>tTa | p.S1692L |
SKCM | 23 | 41069821 | 41069821 | + | Missense_Mutation | SNP | C | C | T | TCGA-FS-A4F5-06A-11D-A25O-08 | TCGA-FS-A4F5-10B-01D-A25O-08 | g.chrX:41069821C>T | c.5075C>T | c.(5074-5076)tCa>tTa | p.S1692L |
SKCM | 23 | 41075159 | 41075159 | + | Missense_Mutation | SNP | C | C | T | TCGA-FS-A1ZK-06A-11D-A197-08 | TCGA-FS-A1ZK-10A-01D-A199-08 | g.chrX:41075159C>T | c.5339C>T | c.(5338-5340)aCc>aTc | p.T1780I |
SKCM | 23 | 41075484 | 41075484 | + | Silent | SNP | T | T | C | TCGA-D3-A2JO-06A-11D-A196-08 | TCGA-D3-A2JO-10A-01D-A198-08 | g.chrX:41075484T>C | c.5664T>C | c.(5662-5664)aaT>aaC | p.N1888N |
SKCM | 23 | 41084153 | 41084153 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chrX:41084153C>T | c.6910C>T | c.(6910-6912)Cgt>Tgt | p.R2304C |
SKCM | 23 | 41088904 | 41088904 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A3C7-06A-11D-A196-08 | TCGA-D3-A3C7-10A-01D-A198-08 | g.chrX:41088904C>T | c.7303C>T | c.(7303-7305)Cct>Tct | p.P2435S |