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 | 10535274 | 10535274 | + | Missense_Mutation | SNP | G | G | T | TCGA-OR-A5JA-01A-11D-A29I-10 | TCGA-OR-A5JA-10A-01D-A29L-10 | g.chrX:10535274G>T | c.314C>A | c.(313-315)gCc>gAc | p.A105D |
BLCA | 23 | 10417481 | 10417481 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-CF-A47T-01A-11D-A23U-08 | TCGA-CF-A47T-10A-01D-A23U-08 | g.chrX:10417481C>T | c.1931G>A | c.(1930-1932)tGg>tAg | p.W644* |
BLCA | 23 | 10417614 | 10417614 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-ZF-AA4W-01A-12D-A38G-08 | TCGA-ZF-AA4W-10A-01D-A38J-08 | g.chrX:10417614delG | c.1798delC | c.(1798-1800)cacfs | p.H600fs |
BLCA | 23 | 10417654 | 10417654 | + | Silent | SNP | C | C | T | TCGA-FD-A6TC-01A-21D-A339-08 | TCGA-FD-A6TC-10A-21D-A339-08 | g.chrX:10417654C>T | c.1758G>A | c.(1756-1758)gtG>gtA | p.V586V |
BLCA | 23 | 10427830 | 10427830 | + | Missense_Mutation | SNP | C | C | G | TCGA-GV-A3JX-01A-11D-A20D-08 | TCGA-GV-A3JX-10A-01D-A20D-08 | g.chrX:10427830C>G | c.1303G>C | c.(1303-1305)Gat>Cat | p.D435H |
BLCA | 23 | 10450524 | 10450524 | + | Missense_Mutation | SNP | C | C | T | TCGA-FD-A6TC-01A-21D-A339-08 | TCGA-FD-A6TC-10A-21D-A339-08 | g.chrX:10450524C>T | c.1009G>A | c.(1009-1011)Gag>Aag | p.E337K |
BLCA | 23 | 10534931 | 10534931 | + | Silent | SNP | C | C | T | TCGA-ZF-AA4V-01A-11D-A38G-08 | TCGA-ZF-AA4V-10A-01D-A38J-08 | g.chrX:10534931C>T | c.657G>A | c.(655-657)ttG>ttA | p.L219L |
BLCA | 23 | 10534939 | 10534939 | + | Missense_Mutation | SNP | C | C | T | TCGA-FD-A5BZ-01A-11D-A289-08 | TCGA-FD-A5BZ-10A-01D-A289-08 | g.chrX:10534939C>T | c.649G>A | c.(649-651)Gac>Aac | p.D217N |
BLCA | 23 | 10535150 | 10535150 | + | Silent | SNP | C | C | T | TCGA-BT-A2LB-01A-11D-A18F-08 | TCGA-BT-A2LB-10A-01D-A18F-08 | g.chrX:10535150C>T | c.438G>A | c.(436-438)ctG>ctA | p.L146L |
BLCA | 23 | 10535154 | 10535154 | + | Missense_Mutation | SNP | C | C | A | TCGA-UY-A9PB-01A-11D-A38G-08 | TCGA-UY-A9PB-10A-01D-A38J-08 | g.chrX:10535154C>A | c.434G>T | c.(433-435)tGc>tTc | p.C145F |
BLCA | 23 | 10535264 | 10535264 | + | Silent | SNP | G | G | T | TCGA-FD-A6TC-01A-21D-A339-08 | TCGA-FD-A6TC-10A-21D-A339-08 | g.chrX:10535264G>T | c.324C>A | c.(322-324)gcC>gcA | p.A108A |
BLCA | 23 | 10535278 | 10535278 | + | Missense_Mutation | SNP | G | G | A | TCGA-XF-A9SU-01A-31D-A391-08 | TCGA-XF-A9SU-10A-01D-A394-08 | g.chrX:10535278G>A | c.310C>T | c.(310-312)Cgg>Tgg | p.R104W |
BRCA | 23 | 10442697 | 10442697 | + | Silent | SNP | C | C | T | TCGA-EW-A1J5-01A-11D-A13L-09 | TCGA-EW-A1J5-10A-01D-A13O-09 | g.chrX:10442697C>T | c.1107G>A | c.(1105-1107)gaG>gaA | p.E369E |
BRCA | 23 | 10442722 | 10442722 | + | Missense_Mutation | SNP | G | G | A | TCGA-E9-A1N9-01A-11D-A14G-09 | TCGA-E9-A1N9-10A-01D-A14G-09 | g.chrX:10442722G>A | c.1082C>T | c.(1081-1083)aCc>aTc | p.T361I |
BRCA | 23 | 10442787 | 10442787 | + | Silent | SNP | G | G | A | TCGA-AN-A046-01A-21W-A050-09 | TCGA-AN-A046-10A-01W-A055-09 | g.chrX:10442787G>A | c.1017C>T | c.(1015-1017)gtC>gtT | p.V339V |
BRCA | 23 | 10450569 | 10450569 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-BH-A0HF-01A-11W-A071-09 | TCGA-BH-A0HF-10A-01W-A071-09 | g.chrX:10450569C>A | c.964G>T | c.(964-966)Gag>Tag | p.E322* |
BRCA | 23 | 10491176 | 10491176 | + | Missense_Mutation | SNP | C | C | G | TCGA-E9-A1RG-01A-11D-A14G-09 | TCGA-E9-A1RG-10A-01D-A14G-09 | g.chrX:10491176C>G | c.712G>C | c.(712-714)Gag>Cag | p.E238Q |
BRCA | 23 | 10534972 | 10534972 | + | Missense_Mutation | SNP | C | C | T | TCGA-BH-A0C1-01B-11D-A12B-09 | TCGA-BH-A0C1-10A-01D-A12B-09 | g.chrX:10534972C>T | c.616G>A | c.(616-618)Gat>Aat | p.D206N |
BRCA | 23 | 10535215 | 10535215 | + | Missense_Mutation | SNP | C | C | T | TCGA-GM-A2DN-01A-11D-A17W-09 | TCGA-GM-A2DN-10C-01D-A17W-09 | g.chrX:10535215C>T | c.373G>A | c.(373-375)Gat>Aat | p.D125N |
BRCA | 23 | 10535323 | 10535323 | + | Missense_Mutation | SNP | C | C | T | TCGA-A8-A07W-01A-11W-A019-09 | TCGA-A8-A07W-10A-01W-A021-09 | g.chrX:10535323C>T | c.265G>A | c.(265-267)Gca>Aca | p.A89T |
BRCA | 23 | 10535364 | 10535364 | + | Missense_Mutation | SNP | C | C | T | TCGA-B6-A40B-01A-11D-A23C-09 | TCGA-B6-A40B-10A-01D-A23C-09 | g.chrX:10535364C>T | c.224G>A | c.(223-225)cGc>cAc | p.R75H |
BRCA | 23 | 10535385 | 10535385 | + | Missense_Mutation | SNP | C | C | T | TCGA-BH-A0B6-01A-11D-A19Y-09 | TCGA-BH-A0B6-10A-01D-A19Y-09 | g.chrX:10535385C>T | c.203G>A | c.(202-204)cGa>cAa | p.R68Q |
CESC | 23 | 10535234 | 10535234 | + | Silent | SNP | G | G | C | TCGA-EK-A3GK-01A-11D-A20U-09 | TCGA-EK-A3GK-10A-01D-A20U-09 | g.chrX:10535234G>C | c.354C>G | c.(352-354)ctC>ctG | p.L118L |
CHOL | 23 | 10422989 | 10422989 | + | Missense_Mutation | SNP | C | C | A | TCGA-4G-AAZO-01A-12D-A417-09 | TCGA-4G-AAZO-11A-11D-A41A-09 | g.chrX:10422989C>A | c.1576G>T | c.(1576-1578)Ggg>Tgg | p.G526W |
COAD | 23 | 10417723 | 10417723 | + | Silent | SNP | C | C | T | TCGA-AY-5543-01A-01D-1650-10 | TCGA-AY-5543-10A-01D-1650-10 | g.chrX:10417723C>T | c.1689G>A | c.(1687-1689)ccG>ccA | p.P563P |
COAD | 23 | 10422949 | 10422949 | + | Missense_Mutation | SNP | C | C | T | TCGA-AD-6895-01A-11D-1924-10 | TCGA-AD-6895-10A-01D-1924-10 | g.chrX:10422949C>T | c.1616G>A | c.(1615-1617)gGc>gAc | p.G539D |
COAD | 23 | 10437807 | 10437807 | + | Silent | SNP | G | G | A | TCGA-AD-6895-01A-11D-1924-10 | TCGA-AD-6895-10A-01D-1924-10 | g.chrX:10437807G>A | c.1215C>T | c.(1213-1215)tcC>tcT | p.S405S |
COAD | 23 | 10463676 | 10463676 | + | Missense_Mutation | SNP | T | T | C | TCGA-D5-6536-01A-11D-1719-10 | TCGA-D5-6536-10A-01D-1719-10 | g.chrX:10463676T>C | c.812A>G | c.(811-813)gAg>gGg | p.E271G |
COAD | 23 | 10491220 | 10491220 | + | Missense_Mutation | SNP | A | A | G | TCGA-D5-6533-01A-11D-1719-10 | TCGA-D5-6533-10A-01D-1719-10 | g.chrX:10491220A>G | c.668T>C | c.(667-669)tTa>tCa | p.L223S |
COAD | 23 | 10534981 | 10534981 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3812-01A-01W-0900-09 | TCGA-AA-3812-10A-01W-0900-09 | g.chrX:10534981G>A | c.607C>T | c.(607-609)Cgg>Tgg | p.R203W |
COAD | 23 | 10535192 | 10535192 | + | Missense_Mutation | SNP | C | C | G | TCGA-AA-3542-01A-02W-0831-10 | TCGA-AA-3542-10A-01W-0831-10 | g.chrX:10535192C>G | c.396G>C | c.(394-396)aaG>aaC | p.K132N |
COADREAD | 23 | 10417466 | 10417466 | + | Missense_Mutation | SNP | G | G | A | TCGA-EI-6508-01A-11D-1733-10 | TCGA-EI-6508-10A-01D-1733-10 | g.chrX:10417466G>A | c.1946C>T | c.(1945-1947)aCg>aTg | p.T649M |
COADREAD | 23 | 10417522 | 10417522 | + | Silent | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chrX:10417522G>A | c.1890C>T | c.(1888-1890)gaC>gaT | p.D630D |
COADREAD | 23 | 10417723 | 10417723 | + | Silent | SNP | C | C | T | TCGA-AY-5543-01A-01D-1650-10 | TCGA-AY-5543-10A-01D-1650-10 | g.chrX:10417723C>T | c.1689G>A | c.(1687-1689)ccG>ccA | p.P563P |
COADREAD | 23 | 10422949 | 10422949 | + | Missense_Mutation | SNP | C | C | T | TCGA-AD-6895-01A-11D-1924-10 | TCGA-AD-6895-10A-01D-1924-10 | g.chrX:10422949C>T | c.1616G>A | c.(1615-1617)gGc>gAc | p.G539D |
COADREAD | 23 | 10427780 | 10427780 | + | Silent | SNP | G | G | A | TCGA-EI-6506-01A-11D-1733-10 | TCGA-EI-6506-10A-01D-1733-10 | g.chrX:10427780G>A | c.1353C>T | c.(1351-1353)caC>caT | p.H451H |
COADREAD | 23 | 10437807 | 10437807 | + | Silent | SNP | G | G | A | TCGA-AD-6895-01A-11D-1924-10 | TCGA-AD-6895-10A-01D-1924-10 | g.chrX:10437807G>A | c.1215C>T | c.(1213-1215)tcC>tcT | p.S405S |
COADREAD | 23 | 10463676 | 10463676 | + | Missense_Mutation | SNP | T | T | C | TCGA-D5-6536-01A-11D-1719-10 | TCGA-D5-6536-10A-01D-1719-10 | g.chrX:10463676T>C | c.812A>G | c.(811-813)gAg>gGg | p.E271G |
COADREAD | 23 | 10491220 | 10491220 | + | Missense_Mutation | SNP | A | A | G | TCGA-D5-6533-01A-11D-1719-10 | TCGA-D5-6533-10A-01D-1719-10 | g.chrX:10491220A>G | c.668T>C | c.(667-669)tTa>tCa | p.L223S |
COADREAD | 23 | 10534931 | 10534931 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chrX:10534931C>A | c.657G>T | c.(655-657)ttG>ttT | p.L219F |
COADREAD | 23 | 10534981 | 10534981 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3812-01A-01W-0900-09 | TCGA-AA-3812-10A-01W-0900-09 | g.chrX:10534981G>A | c.607C>T | c.(607-609)Cgg>Tgg | p.R203W |
COADREAD | 23 | 10535192 | 10535192 | + | Missense_Mutation | SNP | C | C | G | TCGA-AA-3542-01A-02W-0831-10 | TCGA-AA-3542-10A-01W-0831-10 | g.chrX:10535192C>G | c.396G>C | c.(394-396)aaG>aaC | p.K132N |
COADREAD | 23 | 10535339 | 10535339 | + | Silent | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chrX:10535339G>A | c.249C>T | c.(247-249)atC>atT | p.I83I |
ESCA | 23 | 10417677 | 10417677 | + | Missense_Mutation | SNP | G | G | A | TCGA-LN-A4A3-01A-11D-A27G-09 | TCGA-LN-A4A3-10A-01D-A27G-09 | g.chrX:10417677G>A | c.1735C>T | c.(1735-1737)Cgc>Tgc | p.R579C |
ESCA | 23 | 10437871 | 10437871 | + | Missense_Mutation | SNP | G | G | T | TCGA-L5-A4OJ-01A-11D-A27G-09 | TCGA-L5-A4OJ-11A-12D-A27G-09 | g.chrX:10437871G>T | c.1151C>A | c.(1150-1152)cCt>cAt | p.P384H |
ESCA | 23 | 10535076 | 10535076 | + | Missense_Mutation | SNP | C | C | A | TCGA-JY-A6FH-01A-11D-A33E-09 | TCGA-JY-A6FH-10A-01D-A33H-09 | g.chrX:10535076C>A | c.512G>T | c.(511-513)cGg>cTg | p.R171L |
GBM | 23 | 10535512 | 10535512 | + | Missense_Mutation | SNP | C | C | T | TCGA-14-0862-01B-01D-1845-08 | TCGA-14-0862-10C-01D-1845-08 | g.chrX:10535512C>T | c.76G>A | c.(76-78)Gca>Aca | p.A26T |
GBMLGG | 23 | 10417629 | 10417629 | + | Missense_Mutation | SNP | T | T | C | TCGA-HT-A5R9-01A-11D-A289-08 | TCGA-HT-A5R9-10A-01D-A289-08 | g.chrX:10417629T>C | c.1783A>G | c.(1783-1785)Att>Gtt | p.I595V |
GBMLGG | 23 | 10442675 | 10442675 | + | Missense_Mutation | SNP | C | C | G | TCGA-P5-A780-01A-12D-A32B-08 | TCGA-P5-A780-10A-01D-A329-08 | g.chrX:10442675C>G | c.1129G>C | c.(1129-1131)Gat>Cat | p.D377H |
GBMLGG | 23 | 10534972 | 10534972 | + | Missense_Mutation | SNP | C | C | T | TCGA-HT-A5RC-01A-11D-A289-08 | TCGA-HT-A5RC-10A-01D-A289-08 | g.chrX:10534972C>T | c.616G>A | c.(616-618)Gat>Aat | p.D206N |
GBMLGG | 23 | 10535405 | 10535405 | + | Silent | SNP | A | A | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chrX:10535405A>G | c.183T>C | c.(181-183)caT>caC | p.H61H |
GBMLGG | 23 | 10535512 | 10535512 | + | Missense_Mutation | SNP | C | C | T | TCGA-14-0862-01B-01D-1845-08 | TCGA-14-0862-10C-01D-1845-08 | g.chrX:10535512C>T | c.76G>A | c.(76-78)Gca>Aca | p.A26T |
HNSC | 23 | 10437743 | 10437743 | + | Missense_Mutation | SNP | C | C | T | TCGA-CV-7101-01A-11D-2012-08 | TCGA-CV-7101-10A-01D-2013-08 | g.chrX:10437743C>T | c.1279G>A | c.(1279-1281)Gtc>Atc | p.V427I |
HNSC | 23 | 10442739 | 10442739 | + | Silent | SNP | G | G | A | TCGA-UF-A7JT-01A-11D-A34J-08 | TCGA-UF-A7JT-10A-01D-A34M-08 | g.chrX:10442739G>A | c.1065C>T | c.(1063-1065)ctC>ctT | p.L355L |
HNSC | 23 | 10463668 | 10463668 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-MT-A67F-01A-11D-A30E-08 | TCGA-MT-A67F-10A-01D-A30H-08 | g.chrX:10463668G>A | c.820C>T | c.(820-822)Cag>Tag | p.Q274* |
HNSC | 23 | 10535569 | 10535569 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-HD-7753-01A-11D-2078-08 | TCGA-HD-7753-10A-01D-2078-08 | g.chrX:10535569C>A | c.19G>T | c.(19-21)Gaa>Taa | p.E7* |
KIPAN | 23 | 10427708 | 10427708 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-CZ-5453-01A-01D-1501-10 | TCGA-CZ-5453-11A-01D-1501-10 | g.chrX:10427708delC | c.1425delG | c.(1423-1425)gagfs | p.E475fs |
KIPAN | 23 | 10535072 | 10535072 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-F9-A7VF-01A-11D-A33Q-10 | TCGA-F9-A7VF-10A-01D-A33Q-10 | g.chrX:10535072delC | c.516delG | c.(514-516)gggfs | p.G172fs |
KIRC | 23 | 10427708 | 10427708 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-CZ-5453-01A-01D-1501-10 | TCGA-CZ-5453-11A-01D-1501-10 | g.chrX:10427708delC | c.1425delG | c.(1423-1425)gagfs | p.E475fs |
KIRP | 23 | 10535072 | 10535072 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-F9-A7VF-01A-11D-A33Q-10 | TCGA-F9-A7VF-10A-01D-A33Q-10 | g.chrX:10535072delC | c.516delG | c.(514-516)gggfs | p.G172fs |
LGG | 23 | 10417629 | 10417629 | + | Missense_Mutation | SNP | T | T | C | TCGA-HT-A5R9-01A-11D-A289-08 | TCGA-HT-A5R9-10A-01D-A289-08 | g.chrX:10417629T>C | c.1783A>G | c.(1783-1785)Att>Gtt | p.I595V |
LGG | 23 | 10442675 | 10442675 | + | Missense_Mutation | SNP | C | C | G | TCGA-P5-A780-01A-12D-A32B-08 | TCGA-P5-A780-10A-01D-A329-08 | g.chrX:10442675C>G | c.1129G>C | c.(1129-1131)Gat>Cat | p.D377H |
LGG | 23 | 10534972 | 10534972 | + | Missense_Mutation | SNP | C | C | T | TCGA-HT-A5RC-01A-11D-A289-08 | TCGA-HT-A5RC-10A-01D-A289-08 | g.chrX:10534972C>T | c.616G>A | c.(616-618)Gat>Aat | p.D206N |
LGG | 23 | 10535405 | 10535405 | + | Silent | SNP | A | A | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chrX:10535405A>G | c.183T>C | c.(181-183)caT>caC | p.H61H |
LIHC | 23 | 10437803 | 10437803 | + | Missense_Mutation | SNP | C | C | T | TCGA-ES-A2HS-01A-11D-A183-10 | TCGA-ES-A2HS-11A-11D-A183-10 | g.chrX:10437803C>T | c.1219G>A | c.(1219-1221)Gat>Aat | p.D407N |
LIHC | 23 | 10450648 | 10450648 | + | Silent | SNP | C | C | A | TCGA-EP-A2KA-01A-11D-A183-10 | TCGA-EP-A2KA-10A-01D-A183-10 | g.chrX:10450648C>A | c.885G>T | c.(883-885)ctG>ctT | p.L295L |
LIHC | 23 | 10535300 | 10535300 | + | Silent | SNP | A | A | T | TCGA-DD-AADA-01A-11D-A40R-10 | TCGA-DD-AADA-10A-01D-A40U-10 | g.chrX:10535300A>T | c.288T>A | c.(286-288)tcT>tcA | p.S96S |
LUAD | 23 | 10417702 | 10417702 | + | Missense_Mutation | SNP | C | C | A | TCGA-55-8506-01A-11D-2393-08 | TCGA-55-8506-10A-01D-2393-08 | g.chrX:10417702C>A | c.1710G>T | c.(1708-1710)aaG>aaT | p.K570N |
LUAD | 23 | 10417750 | 10417750 | + | Silent | SNP | G | G | T | TCGA-97-7938-01A-11D-2167-08 | TCGA-97-7938-10A-01D-2167-08 | g.chrX:10417750G>T | c.1662C>A | c.(1660-1662)gcC>gcA | p.A554A |
LUAD | 23 | 10423042 | 10423042 | + | Missense_Mutation | SNP | C | C | A | TCGA-69-A59K-01A-11D-A25L-08 | TCGA-69-A59K-10A-01D-A25L-08 | g.chrX:10423042C>A | c.1523G>T | c.(1522-1524)cGt>cTt | p.R508L |
LUAD | 23 | 10423046 | 10423046 | + | Missense_Mutation | SNP | C | C | G | TCGA-69-7980-01A-11D-2184-08 | TCGA-69-7980-10A-01D-2184-08 | g.chrX:10423046C>G | c.1519G>C | c.(1519-1521)Gaa>Caa | p.E507Q |
LUAD | 23 | 10423065 | 10423065 | + | Silent | SNP | G | G | C | TCGA-MP-A4TF-01A-11D-A25L-08 | TCGA-MP-A4TF-10A-01D-A25L-08 | g.chrX:10423065G>C | c.1500C>G | c.(1498-1500)tcC>tcG | p.S500S |
LUAD | 23 | 10427696 | 10427696 | + | Silent | SNP | C | C | T | TCGA-49-6743-01A-11D-1855-08 | TCGA-49-6743-11A-01D-1855-08 | g.chrX:10427696C>T | c.1437G>A | c.(1435-1437)ttG>ttA | p.L479L |
LUAD | 23 | 10442753 | 10442753 | + | Missense_Mutation | SNP | G | G | T | TCGA-69-7980-01A-11D-2184-08 | TCGA-69-7980-10A-01D-2184-08 | g.chrX:10442753G>T | c.1051C>A | c.(1051-1053)Cct>Act | p.P351T |
LUAD | 23 | 10450570 | 10450570 | + | Silent | SNP | C | C | T | TCGA-55-8203-01A-11D-2238-08 | TCGA-55-8203-10A-01D-2238-08 | g.chrX:10450570C>T | c.963G>A | c.(961-963)aaG>aaA | p.K321K |
LUAD | 23 | 10535195 | 10535195 | + | Silent | SNP | C | C | T | TCGA-55-7995-01A-11D-2184-08 | TCGA-55-7995-10A-01D-2184-08 | g.chrX:10535195C>T | c.393G>A | c.(391-393)gtG>gtA | p.V131V |
LUAD | 23 | 10535287 | 10535287 | + | Missense_Mutation | SNP | G | G | T | TCGA-05-4427-01A-21D-1855-08 | TCGA-05-4427-10A-01D-1855-08 | g.chrX:10535287G>T | c.301C>A | c.(301-303)Cgt>Agt | p.R101S |
LUAD | 23 | 10535314 | 10535314 | + | Missense_Mutation | SNP | T | T | C | TCGA-17-Z003-01A-01W-0746-08 | TCGA-17-Z003-11A-01W-0746-08 | g.chrX:10535314T>C | c.274A>G | c.(274-276)Agc>Ggc | p.S92G |
LUAD | 23 | 10535315 | 10535315 | + | Silent | SNP | C | C | A | TCGA-86-8073-01A-11D-2238-08 | TCGA-86-8073-10A-01D-2238-08 | g.chrX:10535315C>A | c.273G>T | c.(271-273)gtG>gtT | p.V91V |
LUAD | 23 | 10535354 | 10535354 | + | Silent | SNP | G | G | C | TCGA-78-7220-01A-11D-2036-08 | TCGA-78-7220-10A-01D-2036-08 | g.chrX:10535354G>C | c.234C>G | c.(232-234)acC>acG | p.T78T |
LUAD | 23 | 10535481 | 10535481 | + | Missense_Mutation | SNP | C | C | A | TCGA-78-7220-01A-11D-2036-08 | TCGA-78-7220-10A-01D-2036-08 | g.chrX:10535481C>A | c.107G>T | c.(106-108)cGc>cTc | p.R36L |
LUAD | 23 | 10535483 | 10535483 | + | Missense_Mutation | SNP | G | G | T | TCGA-78-7220-01A-11D-2036-08 | TCGA-78-7220-10A-01D-2036-08 | g.chrX:10535483G>T | c.105C>A | c.(103-105)caC>caA | p.H35Q |
LUSC | 23 | 10450578 | 10450578 | + | Missense_Mutation | SNP | A | A | T | TCGA-21-5782-01A-01D-1632-08 | TCGA-21-5782-10A-01D-1632-08 | g.chrX:10450578A>T | c.955T>A | c.(955-957)Tct>Act | p.S319T |
LUSC | 23 | 10535112 | 10535112 | + | Missense_Mutation | SNP | T | T | C | TCGA-34-5236-01A-21D-1817-08 | TCGA-34-5236-10A-01D-1817-08 | g.chrX:10535112T>C | c.476A>G | c.(475-477)cAt>cGt | p.H159R |
OV | 23 | 10437842 | 10437842 | + | Missense_Mutation | SNP | C | C | G | TCGA-09-2056-01B-01W-0722-08 | TCGA-09-2056-11A-01W-0722-08 | g.chrX:10437842C>G | c.1180G>C | c.(1180-1182)Gct>Cct | p.A394P |
OV | 23 | 10463677 | 10463677 | + | Missense_Mutation | SNP | C | C | G | TCGA-13-0762-01A-01W-0370-10 | TCGA-13-0762-10A-01W-0370-10 | g.chrX:10463677C>G | c.811G>C | c.(811-813)Gag>Cag | p.E271Q |
PAAD | 23 | 10417463 | 10417463 | + | Missense_Mutation | SNP | A | A | C | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chrX:10417463A>C | c.1949T>G | c.(1948-1950)aTt>aGt | p.I650S |
PAAD | 23 | 10427733 | 10427733 | + | Missense_Mutation | SNP | T | T | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chrX:10427733T>A | c.1400A>T | c.(1399-1401)aAc>aTc | p.N467I |
PRAD | 23 | 10417583 | 10417583 | + | Missense_Mutation | SNP | T | T | C | TCGA-YL-A8S8-01A-11D-A377-08 | TCGA-YL-A8S8-10A-01D-A37A-08 | g.chrX:10417583T>C | c.1829A>G | c.(1828-1830)tAt>tGt | p.Y610C |
READ | 23 | 10417466 | 10417466 | + | Missense_Mutation | SNP | G | G | A | TCGA-EI-6508-01A-11D-1733-10 | TCGA-EI-6508-10A-01D-1733-10 | g.chrX:10417466G>A | c.1946C>T | c.(1945-1947)aCg>aTg | p.T649M |
READ | 23 | 10417522 | 10417522 | + | Silent | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chrX:10417522G>A | c.1890C>T | c.(1888-1890)gaC>gaT | p.D630D |
READ | 23 | 10427780 | 10427780 | + | Silent | SNP | G | G | A | TCGA-EI-6506-01A-11D-1733-10 | TCGA-EI-6506-10A-01D-1733-10 | g.chrX:10427780G>A | c.1353C>T | c.(1351-1353)caC>caT | p.H451H |
READ | 23 | 10534931 | 10534931 | + | Missense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chrX:10534931C>A | c.657G>T | c.(655-657)ttG>ttT | p.L219F |
READ | 23 | 10535339 | 10535339 | + | Silent | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chrX:10535339G>A | c.249C>T | c.(247-249)atC>atT | p.I83I |
SARC | 23 | 10535288 | 10535288 | + | Silent | SNP | G | G | A | TCGA-QC-A7B5-01A-11D-A33E-09 | TCGA-QC-A7B5-11A-11D-A33H-09 | g.chrX:10535288G>A | c.300C>T | c.(298-300)acC>acT | p.T100T |
SKCM | 23 | 10417593 | 10417593 | + | Silent | SNP | G | G | A | TCGA-D3-A5GU-06A-11D-A27K-08 | TCGA-D3-A5GU-10A-01D-A27N-08 | g.chrX:10417593G>A | c.1819C>T | c.(1819-1821)Ctg>Ttg | p.L607L |
SKCM | 23 | 10422960 | 10422960 | + | Silent | SNP | A | A | G | TCGA-EE-A29M-06A-11D-A196-08 | TCGA-EE-A29M-10A-01D-A198-08 | g.chrX:10422960A>G | c.1605T>C | c.(1603-1605)ttT>ttC | p.F535F |
SKCM | 23 | 10423070 | 10423070 | + | Missense_Mutation | SNP | C | C | T | TCGA-FS-A1ZA-06A-11D-A197-08 | TCGA-FS-A1ZA-10A-01D-A199-08 | g.chrX:10423070C>T | c.1495G>A | c.(1495-1497)Gtg>Atg | p.V499M |
SKCM | 23 | 10427726 | 10427726 | + | Silent | SNP | C | C | T | TCGA-EE-A2A2-06A-11D-A196-08 | TCGA-EE-A2A2-10A-01D-A198-08 | g.chrX:10427726C>T | c.1407G>A | c.(1405-1407)gcG>gcA | p.A469A |
SKCM | 23 | 10427798 | 10427798 | + | Silent | SNP | C | C | T | TCGA-EE-A3J5-06A-11D-A20D-08 | TCGA-EE-A3J5-10A-01D-A20D-08 | g.chrX:10427798C>T | c.1335G>A | c.(1333-1335)caG>caA | p.Q445Q |
SKCM | 23 | 10463689 | 10463689 | + | Missense_Mutation | SNP | C | C | T | TCGA-FS-A1ZZ-06A-11D-A197-08 | TCGA-FS-A1ZZ-10A-01D-A199-08 | g.chrX:10463689C>T | c.799G>A | c.(799-801)Gat>Aat | p.D267N |