Mutation - TCGA |
Type | Chromosome | Start Position | End Position | Strand | Variant Classification | Variant Type | Reference Allele | Tumor_seq Allele 1 | Tumor_seq Allele 2 | Tumor Sample Barcode | Matched Norm Sample Barcode | Genome Change | cDNA Change | Codon Change | Protein Change |
BLCA | 16 | 2752370 | 2752370 | + | Missense_Mutation | SNP | C | C | A | TCGA-FD-A5BT-01A-11D-A26M-08 | TCGA-FD-A5BT-10A-01D-A26K-08 | g.chr16:2752370C>A | c.566C>A | c.(565-567)tCc>tAc | p.S189Y |
BRCA | 16 | 2745959 | 2745959 | + | Silent | SNP | C | C | T | TCGA-OL-A5RX-01A-11D-A28B-09 | TCGA-OL-A5RX-10A-01D-A28E-09 | g.chr16:2745959C>T | c.276C>T | c.(274-276)atC>atT | p.I92I |
COAD | 16 | 2732704 | 2732704 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-6648-01A-11D-1771-10 | TCGA-A6-6648-10A-01D-1771-10 | g.chr16:2732704G>A | c.155G>A | c.(154-156)gGc>gAc | p.G52D |
COAD | 16 | 2749901 | 2749901 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3492-01A-01D-1408-10 | TCGA-AA-3492-11A-01D-1408-10 | g.chr16:2749901G>A | c.533G>A | c.(532-534)gGc>gAc | p.G178D |
COADREAD | 16 | 2732704 | 2732704 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-6648-01A-11D-1771-10 | TCGA-A6-6648-10A-01D-1771-10 | g.chr16:2732704G>A | c.155G>A | c.(154-156)gGc>gAc | p.G52D |
COADREAD | 16 | 2749901 | 2749901 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3492-01A-01D-1408-10 | TCGA-AA-3492-11A-01D-1408-10 | g.chr16:2749901G>A | c.533G>A | c.(532-534)gGc>gAc | p.G178D |
ESCA | 16 | 2749901 | 2749901 | + | Missense_Mutation | SNP | G | G | A | TCGA-L5-A8NV-01A-11D-A37C-09 | TCGA-L5-A8NV-11A-11D-A37F-09 | g.chr16:2749901G>A | c.533G>A | c.(532-534)gGc>gAc | p.G178D |
ESCA | 16 | 2752446 | 2752446 | + | Silent | SNP | C | C | T | TCGA-JY-A6FB-01A-11D-A33E-09 | TCGA-JY-A6FB-10A-01D-A33H-09 | g.chr16:2752446C>T | c.642C>T | c.(640-642)taC>taT | p.Y214Y |
GBMLGG | 16 | 2747985 | 2747985 | + | Missense_Mutation | SNP | G | G | A | TCGA-QH-A65X-01A-11D-A32B-08 | TCGA-QH-A65X-10D-01D-A329-08 | g.chr16:2747985G>A | c.440G>A | c.(439-441)aGc>aAc | p.S147N |
LGG | 16 | 2747985 | 2747985 | + | Missense_Mutation | SNP | G | G | A | TCGA-QH-A65X-01A-11D-A32B-08 | TCGA-QH-A65X-10D-01D-A329-08 | g.chr16:2747985G>A | c.440G>A | c.(439-441)aGc>aAc | p.S147N |
LUAD | 16 | 2732724 | 2732724 | + | Missense_Mutation | SNP | C | C | G | TCGA-71-8520-01A-11D-2393-08 | TCGA-71-8520-10A-01D-2393-08 | g.chr16:2732724C>G | c.175C>G | c.(175-177)Cgg>Ggg | p.R59G |
LUAD | 16 | 2749879 | 2749879 | + | Missense_Mutation | SNP | A | A | T | TCGA-75-6214-01A-41D-1945-08 | TCGA-75-6214-10A-01D-1946-08 | g.chr16:2749879A>T | c.511A>T | c.(511-513)Atg>Ttg | p.M171L |
LUAD | 16 | 2752407 | 2752408 | + | Frame_Shift_Del | DEL | CC | CC | - | TCGA-49-6743-01A-11D-1855-08 | TCGA-49-6743-11A-01D-1855-08 | g.chr16:2752407_2752408delCC | c.603_604delCC | c.(601-606)ttcctcfs | p.L202fs |
LUAD | 16 | 2752431 | 2752431 | + | Silent | SNP | G | G | T | TCGA-95-7947-01A-11D-2184-08 | TCGA-95-7947-10A-01D-2184-08 | g.chr16:2752431G>T | c.627G>T | c.(625-627)ctG>ctT | p.L209L |
LUSC | 16 | 2749842 | 2749842 | + | Silent | SNP | C | C | T | TCGA-66-2756-01A-01D-1522-08 | TCGA-66-2756-11A-01D-1522-08 | g.chr16:2749842C>T | c.474C>T | c.(472-474)taC>taT | p.Y158Y |
PCPG | 16 | 2732747 | 2732747 | + | Silent | SNP | G | G | A | TCGA-SP-A6QK-01A-11D-A35I-08 | TCGA-SP-A6QK-10A-01D-A35G-08 | g.chr16:2732747G>A | c.198G>A | c.(196-198)ccG>ccA | p.P66P |
PRAD | 16 | 2752452 | 2752452 | + | Silent | SNP | G | G | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr16:2752452G>A | c.648G>A | c.(646-648)acG>acA | p.T216T |
SKCM | 16 | 2732687 | 2732687 | + | Silent | SNP | C | C | T | TCGA-FS-A1ZZ-06A-11D-A197-08 | TCGA-FS-A1ZZ-10A-01D-A199-08 | g.chr16:2732687C>T | c.138C>T | c.(136-138)gtC>gtT | p.V46V |
SKCM | 16 | 2732753 | 2732753 | + | Silent | SNP | C | C | T | TCGA-GN-A265-06A-21D-A197-08 | TCGA-GN-A265-10A-01D-A199-08 | g.chr16:2732753C>T | c.204C>T | c.(202-204)tcC>tcT | p.S68S |
SKCM | 16 | 2747994 | 2747994 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A2JP-06A-11D-A19A-08 | TCGA-D3-A2JP-10A-01D-A19A-08 | g.chr16:2747994C>T | c.449C>T | c.(448-450)tCg>tTg | p.S150L |
SKCM | 16 | 2749829 | 2749829 | + | Missense_Mutation | SNP | T | T | G | TCGA-FS-A1ZK-06A-11D-A197-08 | TCGA-FS-A1ZK-10A-01D-A199-08 | g.chr16:2749829T>G | c.461T>G | c.(460-462)gTg>gGg | p.V154G |
SKCM | 16 | 2757314 | 2757314 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3J5-06A-11D-A20D-08 | TCGA-EE-A3J5-10A-01D-A20D-08 | g.chr16:2757314G>A | c.691G>A | c.(691-693)Ggc>Agc | p.G231S |
SKCM | 16 | 2757318 | 2757318 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MF-06A-11D-A21A-08 | TCGA-EE-A2MF-10B-01D-A21A-08 | g.chr16:2757318C>T | c.695C>T | c.(694-696)tCa>tTa | p.S232L |