Mutation - TCGA |
Type | Chromosome | Start Position | End Position | Strand | Variant Classification | Variant Type | Reference Allele | Tumor_seq Allele 1 | Tumor_seq Allele 2 | Tumor Sample Barcode | Matched Norm Sample Barcode | Genome Change | cDNA Change | Codon Change | Protein Change |
BLCA | 23 | 153770605 | 153770605 | + | Intron | DEL | G | G | - | TCGA-4Z-AA87-01A-11D-A391-08 | TCGA-4Z-AA87-10A-01D-A394-08 | g.chrX:153770605delG | | | |
BLCA | 23 | 153780345 | 153780345 | + | Missense_Mutation | SNP | C | C | T | TCGA-SY-A9G5-01A-11D-A38G-08 | TCGA-SY-A9G5-10A-01D-A38J-08 | g.chrX:153780345C>T | c.128C>T | c.(127-129)tCa>tTa | p.S43L |
BLCA | 23 | 153780359 | 153780359 | + | Missense_Mutation | SNP | C | C | G | TCGA-FD-A6TC-01A-21D-A339-08 | TCGA-FD-A6TC-10A-21D-A339-08 | g.chrX:153780359C>G | c.142C>G | c.(142-144)Cct>Gct | p.P48A |
COAD | 23 | 153792576 | 153792577 | + | Frame_Shift_Ins | INS | - | - | C | TCGA-CM-6171-01A-11D-1650-10 | TCGA-CM-6171-10A-01D-1650-10 | g.chrX:153792576_153792577insC | c.1160_1161insC | c.(1159-1164)agccccfs | p.SP387fs |
COAD | 23 | 153792577 | 153792577 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-CK-6746-01A-11D-1835-10 | TCGA-CK-6746-10A-01D-1835-10 | g.chrX:153792577delC | c.1161delC | c.(1159-1161)agcfs | p.S387fs |
COADREAD | 23 | 153792576 | 153792577 | + | Frame_Shift_Ins | INS | - | - | C | TCGA-CM-6171-01A-11D-1650-10 | TCGA-CM-6171-10A-01D-1650-10 | g.chrX:153792576_153792577insC | c.1160_1161insC | c.(1159-1164)agccccfs | p.SP387fs |
COADREAD | 23 | 153792577 | 153792577 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-CK-6746-01A-11D-1835-10 | TCGA-CK-6746-10A-01D-1835-10 | g.chrX:153792577delC | c.1161delC | c.(1159-1161)agcfs | p.S387fs |
GBMLGG | 23 | 153780226 | 153780226 | + | Silent | SNP | G | G | A | TCGA-P5-A77X-01A-11D-A32B-08 | TCGA-P5-A77X-10A-01D-A329-08 | g.chrX:153780226G>A | c.9G>A | c.(7-9)agG>agA | p.R3R |
KICH | 23 | 153770612 | 153770612 | + | Intron | SNP | G | G | C | TCGA-KL-8341-01A-11D-2310-10 | TCGA-KL-8341-11A-01D-2310-10 | g.chrX:153770612G>C | | | |
KIPAN | 23 | 153770607 | 153770607 | + | Intron | SNP | G | G | T | TCGA-A3-3311-01A-01D-0966-08 | TCGA-A3-3311-11A-01D-0966-08 | g.chrX:153770607G>T | | | |
KIPAN | 23 | 153770612 | 153770612 | + | Intron | SNP | G | G | C | TCGA-KL-8341-01A-11D-2310-10 | TCGA-KL-8341-11A-01D-2310-10 | g.chrX:153770612G>C | | | |
KIPAN | 23 | 153770658 | 153770658 | + | Intron | SNP | G | G | T | TCGA-MH-A854-01A-11D-A34Z-10 | TCGA-MH-A854-10A-01D-A34Z-10 | g.chrX:153770658G>T | | | |
KIRC | 23 | 153770607 | 153770607 | + | Intron | SNP | G | G | T | TCGA-A3-3311-01A-01D-0966-08 | TCGA-A3-3311-11A-01D-0966-08 | g.chrX:153770607G>T | | | |
KIRP | 23 | 153770658 | 153770658 | + | Intron | SNP | G | G | T | TCGA-MH-A854-01A-11D-A34Z-10 | TCGA-MH-A854-10A-01D-A34Z-10 | g.chrX:153770658G>T | | | |
LGG | 23 | 153780226 | 153780226 | + | Silent | SNP | G | G | A | TCGA-P5-A77X-01A-11D-A32B-08 | TCGA-P5-A77X-10A-01D-A329-08 | g.chrX:153780226G>A | c.9G>A | c.(7-9)agG>agA | p.R3R |
LIHC | 23 | 153770550 | 153770550 | + | 5'UTR | SNP | T | T | C | TCGA-ES-A2HT-01A-12D-A183-10 | TCGA-ES-A2HT-11A-11D-A183-10 | g.chrX:153770550T>C | | | |
LUAD | 23 | 153770605 | 153770608 | + | Intron | DEL | GGGG | GGGG | - | TCGA-86-8669-01A-11D-2393-08 | TCGA-86-8669-10A-01D-2393-08 | g.chrX:153770605_153770608delGGGG | | | |
LUAD | 23 | 153780267 | 153780267 | + | Missense_Mutation | SNP | G | G | C | TCGA-95-A4VN-01A-11D-A25L-08 | TCGA-95-A4VN-10A-01D-A25L-08 | g.chrX:153780267G>C | c.50G>C | c.(49-51)aGt>aCt | p.S17T |
LUAD | 23 | 153780355 | 153780355 | + | Silent | SNP | C | C | A | TCGA-05-4390-01A-02D-1753-08 | TCGA-05-4390-10A-01D-1753-08 | g.chrX:153780355C>A | c.138C>A | c.(136-138)ggC>ggA | p.G46G |
OV | 23 | 153770592 | 153770592 | + | 5'UTR | SNP | G | G | A | TCGA-23-1122-01A-01W-0486-08 | TCGA-23-1122-10A-01W-0486-08 | g.chrX:153770592G>A | | | |