| 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 | 16 | 27483225 | 27483225 | + | Missense_Mutation | SNP | C | C | T | TCGA-OR-A5K4-01A-11D-A29I-10 | TCGA-OR-A5K4-10A-01D-A29L-10 | g.chr16:27483225C>T | c.4370G>A | c.(4369-4371)cGg>cAg | p.R1457Q |
| ACC | 16 | 27503663 | 27503663 | + | Silent | SNP | T | T | C | TCGA-OR-A5LD-01A-11D-A29I-10 | TCGA-OR-A5LD-10A-01D-A29L-10 | g.chr16:27503663T>C | c.3147A>G | c.(3145-3147)ccA>ccG | p.P1049P |
| ACC | 16 | 27512657 | 27512657 | + | Missense_Mutation | SNP | T | T | G | TCGA-OR-A5LB-01A-11D-A29I-10 | TCGA-OR-A5LB-10A-01D-A29L-10 | g.chr16:27512657T>G | c.1916A>C | c.(1915-1917)aAg>aCg | p.K639T |
| ACC | 16 | 27523098 | 27523098 | + | Silent | SNP | C | C | A | TCGA-OR-A5JB-01A-11D-A29I-10 | TCGA-OR-A5JB-10A-01D-A29L-10 | g.chr16:27523098C>A | c.1098G>T | c.(1096-1098)cgG>cgT | p.R366R |
| ACC | 16 | 27549248 | 27549248 | + | Splice_Site | SNP | C | C | A | TCGA-PK-A5HB-01A-11D-A29I-10 | TCGA-PK-A5HB-11A-11D-A29L-10 | g.chr16:27549248C>A | c.609G>T | c.(607-609)aaG>aaT | p.K203N |
| BLCA | 16 | 27472739 | 27472739 | + | Missense_Mutation | SNP | C | C | T | TCGA-E5-A4TZ-01A-11D-A31L-08 | TCGA-E5-A4TZ-10B-01D-A31J-08 | g.chr16:27472739C>T | c.6262G>A | c.(6262-6264)Gac>Aac | p.D2088N |
| BLCA | 16 | 27472877 | 27472877 | + | Missense_Mutation | SNP | C | C | T | TCGA-G2-A2ES-01A-11D-A17V-08 | TCGA-G2-A2ES-11A-31D-A17V-08 | g.chr16:27472877C>T | c.6124G>A | c.(6124-6126)Gag>Aag | p.E2042K |
| BLCA | 16 | 27475748 | 27475748 | + | Missense_Mutation | SNP | G | G | A | TCGA-G2-A2EJ-01A-11D-A17V-08 | TCGA-G2-A2EJ-10A-01D-A17V-08 | g.chr16:27475748G>A | c.5765C>T | c.(5764-5766)gCg>gTg | p.A1922V |
| BLCA | 16 | 27475764 | 27475764 | + | Missense_Mutation | SNP | C | C | T | TCGA-FJ-A3ZE-01A-11D-A23M-08 | TCGA-FJ-A3ZE-10A-01D-A23K-08 | g.chr16:27475764C>T | c.5749G>A | c.(5749-5751)Gaa>Aaa | p.E1917K |
| BLCA | 16 | 27492442 | 27492442 | + | Missense_Mutation | SNP | G | G | A | TCGA-ZF-AA51-01A-21D-A391-08 | TCGA-ZF-AA51-10A-01D-A394-08 | g.chr16:27492442G>A | c.4154C>T | c.(4153-4155)tCt>tTt | p.S1385F |
| BLCA | 16 | 27492457 | 27492457 | + | Missense_Mutation | SNP | G | G | A | TCGA-DK-A6B5-01A-11D-A31L-08 | TCGA-DK-A6B5-10A-01D-A31J-08 | g.chr16:27492457G>A | c.4139C>T | c.(4138-4140)tCa>tTa | p.S1380L |
| BLCA | 16 | 27500923 | 27500923 | + | Splice_Site | SNP | G | G | A | TCGA-XF-AAMF-01A-21D-A42E-08 | TCGA-XF-AAMF-10A-01D-A42H-08 | g.chr16:27500923G>A | c.3293C>T | c.(3292-3294)aCt>aTt | p.T1098I |
| BLCA | 16 | 27503786 | 27503786 | + | Silent | SNP | G | G | A | TCGA-GV-A6ZA-01A-12D-A339-08 | TCGA-GV-A6ZA-10A-01D-A339-08 | g.chr16:27503786G>A | c.3024C>T | c.(3022-3024)tgC>tgT | p.C1008C |
| BLCA | 16 | 27503822 | 27503822 | + | Silent | SNP | C | C | T | TCGA-FD-A43X-01A-11D-A23U-08 | TCGA-FD-A43X-10A-01D-A23U-08 | g.chr16:27503822C>T | c.2988G>A | c.(2986-2988)ttG>ttA | p.L996L |
| BLCA | 16 | 27509995 | 27509995 | + | Silent | SNP | G | G | A | TCGA-UY-A9PE-01A-11D-A38G-08 | TCGA-UY-A9PE-10A-01D-A38J-08 | g.chr16:27509995G>A | c.2121C>T | c.(2119-2121)atC>atT | p.I707I |
| BLCA | 16 | 27512587 | 27512587 | + | Silent | SNP | C | C | T | TCGA-XF-A9T0-01A-11D-A391-08 | TCGA-XF-A9T0-10A-01D-A394-08 | g.chr16:27512587C>T | c.1986G>A | c.(1984-1986)ttG>ttA | p.L662L |
| BLCA | 16 | 27517274 | 27517274 | + | Missense_Mutation | SNP | G | G | C | TCGA-XF-A9T6-01A-11D-A42E-08 | TCGA-XF-A9T6-10A-01D-A42H-08 | g.chr16:27517274G>C | c.1716C>G | c.(1714-1716)gaC>gaG | p.D572E |
| BLCA | 16 | 27517276 | 27517276 | + | Missense_Mutation | SNP | C | C | G | TCGA-XF-A9SG-01A-12D-A42E-08 | TCGA-XF-A9SG-10A-01D-A42H-08 | g.chr16:27517276C>G | c.1714G>C | c.(1714-1716)Gac>Cac | p.D572H |
| BLCA | 16 | 27518206 | 27518206 | + | Missense_Mutation | SNP | C | C | G | TCGA-UY-A8OB-01A-12D-A42E-08 | TCGA-UY-A8OB-11A-12D-A42H-08 | g.chr16:27518206C>G | c.1514G>C | c.(1513-1515)cGg>cCg | p.R505P |
| BLCA | 16 | 27518218 | 27518218 | + | Missense_Mutation | SNP | G | G | A | TCGA-ZF-AA4V-01A-11D-A38G-08 | TCGA-ZF-AA4V-10A-01D-A38J-08 | g.chr16:27518218G>A | c.1502C>T | c.(1501-1503)tCt>tTt | p.S501F |
| BLCA | 16 | 27518439 | 27518439 | + | Missense_Mutation | SNP | C | C | G | TCGA-FD-A3B6-01A-21D-A20D-08 | TCGA-FD-A3B6-10A-01D-A20D-08 | g.chr16:27518439C>G | c.1281G>C | c.(1279-1281)aaG>aaC | p.K427N |
| BLCA | 16 | 27518477 | 27518477 | + | Splice_Site | SNP | C | C | A | TCGA-ZF-A9RL-01A-11D-A38G-08 | TCGA-ZF-A9RL-10A-01D-A38J-08 | g.chr16:27518477C>A | c.1243G>T | c.(1243-1245)Gga>Tga | p.G415* |
| BLCA | 16 | 27518478 | 27518478 | + | Splice_Site | SNP | C | C | A | TCGA-ZF-A9RL-01A-11D-A38G-08 | TCGA-ZF-A9RL-10A-01D-A38J-08 | g.chr16:27518478C>A | | c.e9-1 | |
| BLCA | 16 | 27539998 | 27539998 | + | Silent | SNP | C | C | G | TCGA-MV-A51V-01A-11D-A26M-08 | TCGA-MV-A51V-10A-01D-A26K-08 | g.chr16:27539998C>G | c.894G>C | c.(892-894)ctG>ctC | p.L298L |
| BLCA | 16 | 27544611 | 27544611 | + | Splice_Site | SNP | C | C | A | TCGA-G2-A2EL-01A-12D-A18F-08 | TCGA-G2-A2EL-10A-01D-A18F-08 | g.chr16:27544611C>A | | c.e5+1 | |
| BLCA | 16 | 27544708 | 27544708 | + | Splice_Site | SNP | C | C | T | TCGA-DK-A3WW-01A-22D-A23M-08 | TCGA-DK-A3WW-10A-01D-A23K-08 | g.chr16:27544708C>T | c.753G>A | c.(751-753)agG>agA | p.R251R |
| BLCA | 16 | 27549623 | 27549623 | + | Missense_Mutation | SNP | C | C | G | TCGA-FD-A6TC-01A-21D-A339-08 | TCGA-FD-A6TC-10A-21D-A339-08 | g.chr16:27549623C>G | c.486G>C | c.(484-486)ttG>ttC | p.L162F |
| BLCA | 16 | 27549623 | 27549623 | + | Silent | SNP | C | C | T | TCGA-2F-A9KO-01A-11D-A38G-08 | TCGA-2F-A9KO-11A-12D-A38J-08 | g.chr16:27549623C>T | c.486G>A | c.(484-486)ttG>ttA | p.L162L |
| BLCA | 16 | 27556683 | 27556683 | + | Missense_Mutation | SNP | C | C | T | TCGA-GU-AATP-01A-11D-A391-08 | TCGA-GU-AATP-10A-01D-A394-08 | g.chr16:27556683C>T | c.383G>A | c.(382-384)aGa>aAa | p.R128K |
| BLCA | 16 | 27556790 | 27556790 | + | Silent | SNP | C | C | G | TCGA-FJ-A3ZE-01A-11D-A23M-08 | TCGA-FJ-A3ZE-10A-01D-A23K-08 | g.chr16:27556790C>G | c.276G>C | c.(274-276)gtG>gtC | p.V92V |
| BLCA | 16 | 27556794 | 27556794 | + | Missense_Mutation | SNP | G | G | A | TCGA-CF-A47X-01A-31D-A23U-08 | TCGA-CF-A47X-10A-01D-A23U-08 | g.chr16:27556794G>A | c.272C>T | c.(271-273)cCg>cTg | p.P91L |
| BLCA | 16 | 27561125 | 27561125 | + | Missense_Mutation | SNP | C | C | G | TCGA-G2-A2EL-01A-12D-A18F-08 | TCGA-G2-A2EL-10A-01D-A18F-08 | g.chr16:27561125C>G | c.87G>C | c.(85-87)gaG>gaC | p.E29D |
| BRCA | 16 | 27474860 | 27474860 | + | Splice_Site | SNP | A | A | C | TCGA-A2-A0T5-01A-21D-A099-09 | TCGA-A2-A0T5-10A-01D-A099-09 | g.chr16:27474860A>C | | c.e35+1 | |
| BRCA | 16 | 27475972 | 27475972 | + | Frame_Shift_Del | DEL | G | G | - | TCGA-A8-A09Z-01A-11W-A019-09 | TCGA-A8-A09Z-10A-01W-A021-09 | g.chr16:27475972delG | c.5541delC | c.(5539-5541)cccfs | p.P1847fs |
| BRCA | 16 | 27476706 | 27476706 | + | Missense_Mutation | SNP | C | C | G | TCGA-D8-A1JA-01A-11D-A13L-09 | TCGA-D8-A1JA-10A-01W-A14R-09 | g.chr16:27476706C>G | c.5230G>C | c.(5230-5232)Gag>Cag | p.E1744Q |
| BRCA | 16 | 27480677 | 27480686 | + | Frame_Shift_Del | DEL | ACCACAATGC | ACCACAATGC | - | TCGA-A1-A0SK-01A-12D-A099-09 | TCGA-A1-A0SK-10A-03D-A099-09 | g.chr16:27480677_27480686delACCACAATGC | c.5000_5009delGCATTGTGGT | c.(4999-5010)agcattgtggtcfs | p.SIVV1667fs |
| BRCA | 16 | 27480781 | 27480781 | + | Silent | SNP | C | C | T | TCGA-AO-A03M-01B-11D-A10M-09 | TCGA-AO-A03M-10A-01D-A10M-09 | g.chr16:27480781C>T | c.4905G>A | c.(4903-4905)gtG>gtA | p.V1635V |
| BRCA | 16 | 27483171 | 27483171 | + | Missense_Mutation | SNP | C | C | A | TCGA-AR-A24H-01A-11D-A167-09 | TCGA-AR-A24H-10A-01D-A167-09 | g.chr16:27483171C>A | c.4424G>T | c.(4423-4425)aGc>aTc | p.S1475I |
| BRCA | 16 | 27492404 | 27492404 | + | Missense_Mutation | SNP | C | C | A | TCGA-AR-A24V-01A-21D-A167-09 | TCGA-AR-A24V-10A-01D-A167-09 | g.chr16:27492404C>A | c.4192G>T | c.(4192-4194)Gcc>Tcc | p.A1398S |
| BRCA | 16 | 27494391 | 27494391 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-AN-A046-01A-21W-A050-09 | TCGA-AN-A046-10A-01W-A055-09 | g.chr16:27494391G>A | c.4057C>T | c.(4057-4059)Cga>Tga | p.R1353* |
| BRCA | 16 | 27497439 | 27497439 | + | Missense_Mutation | SNP | T | T | G | TCGA-E2-A1LK-01A-21D-A14G-09 | TCGA-E2-A1LK-11A-12D-A14G-09 | g.chr16:27497439T>G | c.3737A>C | c.(3736-3738)tAc>tCc | p.Y1246S |
| BRCA | 16 | 27499930 | 27499930 | + | Silent | SNP | G | G | C | TCGA-C8-A274-01A-11D-A16D-09 | TCGA-C8-A274-10A-01D-A16D-09 | g.chr16:27499930G>C | c.3456C>G | c.(3454-3456)ctC>ctG | p.L1152L |
| BRCA | 16 | 27506805 | 27506805 | + | Silent | SNP | G | G | A | TCGA-A8-A08A-01A-11W-A019-09 | TCGA-A8-A08A-10A-01W-A021-09 | g.chr16:27506805G>A | c.2359C>T | c.(2359-2361)Ctg>Ttg | p.L787L |
| BRCA | 16 | 27512666 | 27512666 | + | Splice_Site | SNP | C | C | A | TCGA-BH-A18G-01A-11D-A12B-09 | TCGA-BH-A18G-10A-01D-A12B-09 | g.chr16:27512666C>A | | c.e12-1 | |
| BRCA | 16 | 27517273 | 27517273 | + | Missense_Mutation | SNP | T | T | A | TCGA-E9-A22A-01A-11D-A159-09 | TCGA-E9-A22A-10A-01D-A159-09 | g.chr16:27517273T>A | c.1717A>T | c.(1717-1719)Agc>Tgc | p.S573C |
| BRCA | 16 | 27517381 | 27517381 | + | Missense_Mutation | SNP | C | C | T | TCGA-D8-A1JP-01A-11D-A13L-09 | TCGA-D8-A1JP-10A-01D-A13O-09 | g.chr16:27517381C>T | c.1609G>A | c.(1609-1611)Gga>Aga | p.G537R |
| BRCA | 16 | 27556779 | 27556779 | + | Missense_Mutation | SNP | T | T | A | TCGA-C8-A26W-01A-11D-A16D-09 | TCGA-C8-A26W-10A-01D-A16D-09 | g.chr16:27556779T>A | c.287A>T | c.(286-288)gAt>gTt | p.D96V |
| CESC | 16 | 27472703 | 27472703 | + | Missense_Mutation | SNP | C | C | T | TCGA-EK-A2RA-01A-11D-A18J-09 | TCGA-EK-A2RA-10A-01D-A18J-09 | g.chr16:27472703C>T | c.6298G>A | c.(6298-6300)Gag>Aag | p.E2100K |
| CESC | 16 | 27472852 | 27472852 | + | Missense_Mutation | SNP | C | C | T | TCGA-DS-A7WI-01A-12D-A351-09 | TCGA-DS-A7WI-10A-01D-A351-09 | g.chr16:27472852C>T | c.6149G>A | c.(6148-6150)cGc>cAc | p.R2050H |
| CESC | 16 | 27475925 | 27475925 | + | Missense_Mutation | SNP | C | C | T | TCGA-Q1-A73O-01A-11D-A32I-09 | TCGA-Q1-A73O-10B-01D-A32I-09 | g.chr16:27475925C>T | c.5588G>A | c.(5587-5589)cGc>cAc | p.R1863H |
| CESC | 16 | 27475971 | 27475971 | + | Missense_Mutation | SNP | C | C | T | TCGA-EK-A3GK-01A-11D-A20U-09 | TCGA-EK-A3GK-10A-01D-A20U-09 | g.chr16:27475971C>T | c.5542G>A | c.(5542-5544)Gag>Aag | p.E1848K |
| CESC | 16 | 27480781 | 27480781 | + | Silent | SNP | C | C | T | TCGA-IR-A3LL-01A-11D-A20U-09 | TCGA-IR-A3LL-10A-01D-A20U-09 | g.chr16:27480781C>T | c.4905G>A | c.(4903-4905)gtG>gtA | p.V1635V |
| CESC | 16 | 27481442 | 27481442 | + | Missense_Mutation | SNP | C | C | T | TCGA-JX-A3Q0-01A-11D-A21Q-09 | TCGA-JX-A3Q0-10A-01D-A21Q-09 | g.chr16:27481442C>T | c.4801G>A | c.(4801-4803)Gag>Aag | p.E1601K |
| CESC | 16 | 27504033 | 27504033 | + | Splice_Site | SNP | G | G | A | TCGA-JW-A5VG-01A-11D-A28B-09 | TCGA-JW-A5VG-10A-01D-A28E-09 | g.chr16:27504033G>A | c.2878C>T | c.(2878-2880)Cgt>Tgt | p.R960C |
| CESC | 16 | 27517406 | 27517406 | + | Missense_Mutation | SNP | C | C | G | TCGA-EK-A2RA-01A-11D-A18J-09 | TCGA-EK-A2RA-10A-01D-A18J-09 | g.chr16:27517406C>G | c.1584G>C | c.(1582-1584)ttG>ttC | p.L528F |
| CESC | 16 | 27519901 | 27519901 | + | Missense_Mutation | SNP | C | C | G | TCGA-FU-A3HY-01A-11D-A21Q-09 | TCGA-FU-A3HY-10A-01D-A21Q-09 | g.chr16:27519901C>G | c.1202G>C | c.(1201-1203)aGa>aCa | p.R401T |
| CESC | 16 | 27556663 | 27556663 | + | Missense_Mutation | SNP | G | G | A | TCGA-EK-A2RK-01A-11D-A18J-09 | TCGA-EK-A2RK-10A-01D-A18J-09 | g.chr16:27556663G>A | c.403C>T | c.(403-405)Cgc>Tgc | p.R135C |
| CESC | 16 | 27561120 | 27561120 | + | Missense_Mutation | SNP | C | C | T | TCGA-C5-A2LZ-01A-11D-A20U-09 | TCGA-C5-A2LZ-10B-01D-A20U-09 | g.chr16:27561120C>T | c.92G>A | c.(91-93)cGa>cAa | p.R31Q |
| CESC | 16 | 27561137 | 27561137 | + | Missense_Mutation | SNP | C | C | G | TCGA-EK-A3GM-01A-11D-A20U-09 | TCGA-EK-A3GM-10A-01D-A20U-09 | g.chr16:27561137C>G | c.75G>C | c.(73-75)tgG>tgC | p.W25C |
| CHOL | 16 | 27549552 | 27549552 | + | Missense_Mutation | SNP | C | C | T | TCGA-W5-AA39-01A-11D-A417-09 | TCGA-W5-AA39-10A-01D-A41A-09 | g.chr16:27549552C>T | c.557G>A | c.(556-558)cGg>cAg | p.R186Q |
| COAD | 16 | 27472725 | 27472725 | + | Silent | SNP | C | C | T | TCGA-AA-3821-01A-01W-0995-10 | TCGA-AA-3821-10A-01W-0995-10 | g.chr16:27472725C>T | c.6276G>A | c.(6274-6276)cgG>cgA | p.R2092R |
| COAD | 16 | 27473769 | 27473769 | + | Missense_Mutation | SNP | C | C | T | TCGA-CM-6674-01A-11D-1835-10 | TCGA-CM-6674-10A-01D-1835-10 | g.chr16:27473769C>T | c.5963G>A | c.(5962-5964)cGt>cAt | p.R1988H |
| COAD | 16 | 27475831 | 27475831 | + | Silent | SNP | G | G | T | TCGA-AA-3811-01A-01W-0995-10 | TCGA-AA-3811-10A-01W-0995-10 | g.chr16:27475831G>T | c.5682C>A | c.(5680-5682)gcC>gcA | p.A1894A |
| COAD | 16 | 27475894 | 27475894 | + | Silent | SNP | G | G | A | TCGA-G4-6309-01A-21D-1835-10 | TCGA-G4-6309-10A-01D-1835-10 | g.chr16:27475894G>A | c.5619C>T | c.(5617-5619)acC>acT | p.T1873T |
| COAD | 16 | 27475925 | 27475925 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3837-01A-01W-0900-09 | TCGA-AA-3837-10A-01W-0900-09 | g.chr16:27475925C>T | c.5588G>A | c.(5587-5589)cGc>cAc | p.R1863H |
| COAD | 16 | 27476711 | 27476711 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-6780-01A-11D-1835-10 | TCGA-A6-6780-10A-01D-1835-10 | g.chr16:27476711G>A | c.5225C>T | c.(5224-5226)gCc>gTc | p.A1742V |
| COAD | 16 | 27480708 | 27480708 | + | Missense_Mutation | SNP | G | G | A | TCGA-CM-6162-01A-11D-1650-10 | TCGA-CM-6162-10A-01D-1650-10 | g.chr16:27480708G>A | c.4978C>T | c.(4978-4980)Cgc>Tgc | p.R1660C |
| COAD | 16 | 27481682 | 27481682 | + | Missense_Mutation | SNP | T | T | C | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr16:27481682T>C | c.4561A>G | c.(4561-4563)Acg>Gcg | p.T1521A |
| COAD | 16 | 27483106 | 27483106 | + | Missense_Mutation | SNP | C | C | T | TCGA-A6-6653-01A-11D-1771-10 | TCGA-A6-6653-10A-01D-1771-10 | g.chr16:27483106C>T | c.4489G>A | c.(4489-4491)Gtg>Atg | p.V1497M |
| COAD | 16 | 27483108 | 27483108 | + | Missense_Mutation | SNP | A | A | G | TCGA-CM-6674-01A-11D-1835-10 | TCGA-CM-6674-10A-01D-1835-10 | g.chr16:27483108A>G | c.4487T>C | c.(4486-4488)tTc>tCc | p.F1496S |
| COAD | 16 | 27483197 | 27483197 | + | Missense_Mutation | SNP | C | C | A | TCGA-A6-3809-01A-01W-0995-10 | TCGA-A6-3809-11A-01W-0995-10 | g.chr16:27483197C>A | c.4398G>T | c.(4396-4398)aaG>aaT | p.K1466N |
| COAD | 16 | 27492404 | 27492404 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3870-01A-01W-0995-10 | TCGA-AA-3870-10A-01W-0995-10 | g.chr16:27492404C>T | c.4192G>A | c.(4192-4194)Gcc>Acc | p.A1398T |
| COAD | 16 | 27492455 | 27492455 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3864-01A-01W-0995-10 | TCGA-AA-3864-10A-01W-0995-10 | g.chr16:27492455C>T | c.4141G>A | c.(4141-4143)Gcc>Acc | p.A1381T |
| COAD | 16 | 27495566 | 27495566 | + | Missense_Mutation | SNP | T | T | G | TCGA-AA-3561-01A-01W-0831-10 | TCGA-AA-3561-10A-01W-0831-10 | g.chr16:27495566T>G | c.3967A>C | c.(3967-3969)Ata>Cta | p.I1323L |
| COAD | 16 | 27497443 | 27497443 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3949-01A-01W-0995-10 | TCGA-AA-3949-10A-01W-0995-10 | g.chr16:27497443G>A | c.3733C>T | c.(3733-3735)Cgc>Tgc | p.R1245C |
| COAD | 16 | 27499588 | 27499588 | + | Silent | SNP | C | C | T | TCGA-AZ-4682-01B-01D-1408-10 | TCGA-AZ-4682-10A-01D-1408-10 | g.chr16:27499588C>T | c.3660G>A | c.(3658-3660)ctG>ctA | p.L1220L |
| COAD | 16 | 27499589 | 27499589 | + | Missense_Mutation | SNP | A | A | G | TCGA-AY-5543-01A-01D-1650-10 | TCGA-AY-5543-10A-01D-1650-10 | g.chr16:27499589A>G | c.3659T>C | c.(3658-3660)cTg>cCg | p.L1220P |
| COAD | 16 | 27500950 | 27500950 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-6928-01A-11D-1924-10 | TCGA-D5-6928-10A-01D-1924-10 | g.chr16:27500950C>T | c.3266G>A | c.(3265-3267)cGc>cAc | p.R1089H |
| COAD | 16 | 27503681 | 27503681 | + | Silent | SNP | G | G | A | TCGA-AA-3672-01A-01W-0900-09 | TCGA-AA-3672-10A-01W-0900-09 | g.chr16:27503681G>A | c.3129C>T | c.(3127-3129)tgC>tgT | p.C1043C |
| COAD | 16 | 27506767 | 27506767 | + | Silent | SNP | G | G | A | TCGA-CK-6746-01A-11D-1835-10 | TCGA-CK-6746-10A-01D-1835-10 | g.chr16:27506767G>A | c.2397C>T | c.(2395-2397)cgC>cgT | p.R799R |
| COAD | 16 | 27509009 | 27509009 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-A6-3809-01A-01W-0995-10 | TCGA-A6-3809-11A-01W-0995-10 | g.chr16:27509009delT | c.2299delA | c.(2299-2301)agtfs | p.S767fs |
| COAD | 16 | 27509009 | 27509009 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-AD-5900-01A-11D-1650-10 | TCGA-AD-5900-10A-01D-1650-10 | g.chr16:27509009delT | c.2299delA | c.(2299-2301)agtfs | p.S767fs |
| COAD | 16 | 27509009 | 27509009 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-CK-5916-01A-11D-1650-10 | TCGA-CK-5916-10A-01D-1650-10 | g.chr16:27509009delT | c.2299delA | c.(2299-2301)agtfs | p.S767fs |
| COAD | 16 | 27509009 | 27509009 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-F4-6570-01A-11D-1771-10 | TCGA-F4-6570-10A-01D-1771-10 | g.chr16:27509009delT | c.2299delA | c.(2299-2301)agtfs | p.S767fs |
| COAD | 16 | 27509054 | 27509055 | + | Frame_Shift_Del | DEL | GA | GA | - | TCGA-AA-3713-01A-21D-1719-10 | TCGA-AA-3713-11A-01D-1719-10 | g.chr16:27509054_27509055delGA | c.2253_2254delTC | c.(2251-2256)tctcagfs | p.Q752fs |
| COAD | 16 | 27509111 | 27509111 | + | Missense_Mutation | SNP | C | C | A | TCGA-CM-6680-01A-11D-1835-10 | TCGA-CM-6680-10A-01D-1835-10 | g.chr16:27509111C>A | c.2197G>T | c.(2197-2199)Ggg>Tgg | p.G733W |
| COAD | 16 | 27509117 | 27509117 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr16:27509117G>A | c.2191C>T | c.(2191-2193)Ccc>Tcc | p.P731S |
| COAD | 16 | 27512529 | 27512529 | + | Missense_Mutation | SNP | C | C | A | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr16:27512529C>A | c.2044G>T | c.(2044-2046)Gat>Tat | p.D682Y |
| COAD | 16 | 27512546 | 27512546 | + | Missense_Mutation | SNP | C | C | T | TCGA-A6-5665-01A-01D-1650-10 | TCGA-A6-5665-10A-01D-1650-10 | g.chr16:27512546C>T | c.2027G>A | c.(2026-2028)cGg>cAg | p.R676Q |
| COAD | 16 | 27514180 | 27514180 | + | Splice_Site | SNP | G | G | A | TCGA-CM-6171-01A-11D-1650-10 | TCGA-CM-6171-10A-01D-1650-10 | g.chr16:27514180G>A | c.1907C>T | c.(1906-1908)aCg>aTg | p.T636M |
| COAD | 16 | 27517276 | 27517276 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A00A-01A-01W-A005-10 | TCGA-AA-A00A-10A-01W-A005-10 | g.chr16:27517276C>T | c.1714G>A | c.(1714-1716)Gac>Aac | p.D572N |
| COAD | 16 | 27517363 | 27517364 | + | Frame_Shift_Del | DEL | CT | CT | - | TCGA-AA-3672-01A-01W-0900-09 | TCGA-AA-3672-10A-01W-0900-09 | g.chr16:27517363_27517364delCT | c.1626_1627delAG | c.(1624-1629)agagccfs | p.RA542fs |
| COAD | 16 | 27518173 | 27518173 | + | Missense_Mutation | SNP | G | G | C | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr16:27518173G>C | c.1547C>G | c.(1546-1548)aCc>aGc | p.T516S |
| COAD | 16 | 27523104 | 27523104 | + | Silent | SNP | G | G | A | TCGA-AA-3510-01A-01D-1408-10 | TCGA-AA-3510-11A-01D-1408-10 | g.chr16:27523104G>A | c.1092C>T | c.(1090-1092)ttC>ttT | p.F364F |
| COAD | 16 | 27523175 | 27523175 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-6653-01A-11D-1771-10 | TCGA-A6-6653-10A-01D-1771-10 | g.chr16:27523175G>A | c.1021C>T | c.(1021-1023)Cgg>Tgg | p.R341W |
| COAD | 16 | 27556754 | 27556754 | + | Silent | SNP | T | T | C | TCGA-AA-A022-01A-21W-A096-10 | TCGA-AA-A022-11A-11W-A096-10 | g.chr16:27556754T>C | c.312A>G | c.(310-312)ttA>ttG | p.L104L |
| COAD | 16 | 27556783 | 27556783 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-D5-6540-01A-11D-1719-10 | TCGA-D5-6540-10A-01D-1719-10 | g.chr16:27556783C>A | c.283G>T | c.(283-285)Gag>Tag | p.E95* |
| COADREAD | 16 | 27472725 | 27472725 | + | Silent | SNP | C | C | T | TCGA-AA-3821-01A-01W-0995-10 | TCGA-AA-3821-10A-01W-0995-10 | g.chr16:27472725C>T | c.6276G>A | c.(6274-6276)cgG>cgA | p.R2092R |
| COADREAD | 16 | 27473769 | 27473769 | + | Missense_Mutation | SNP | C | C | T | TCGA-CM-6674-01A-11D-1835-10 | TCGA-CM-6674-10A-01D-1835-10 | g.chr16:27473769C>T | c.5963G>A | c.(5962-5964)cGt>cAt | p.R1988H |
| COADREAD | 16 | 27475831 | 27475831 | + | Silent | SNP | G | G | T | TCGA-AA-3811-01A-01W-0995-10 | TCGA-AA-3811-10A-01W-0995-10 | g.chr16:27475831G>T | c.5682C>A | c.(5680-5682)gcC>gcA | p.A1894A |
| COADREAD | 16 | 27475894 | 27475894 | + | Silent | SNP | G | G | A | TCGA-G4-6309-01A-21D-1835-10 | TCGA-G4-6309-10A-01D-1835-10 | g.chr16:27475894G>A | c.5619C>T | c.(5617-5619)acC>acT | p.T1873T |
| COADREAD | 16 | 27475925 | 27475925 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3837-01A-01W-0900-09 | TCGA-AA-3837-10A-01W-0900-09 | g.chr16:27475925C>T | c.5588G>A | c.(5587-5589)cGc>cAc | p.R1863H |
| COADREAD | 16 | 27476025 | 27476025 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr16:27476025C>A | c.5488G>T | c.(5488-5490)Gaa>Taa | p.E1830* |
| COADREAD | 16 | 27476711 | 27476711 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-6780-01A-11D-1835-10 | TCGA-A6-6780-10A-01D-1835-10 | g.chr16:27476711G>A | c.5225C>T | c.(5224-5226)gCc>gTc | p.A1742V |
| COADREAD | 16 | 27480708 | 27480708 | + | Missense_Mutation | SNP | G | G | A | TCGA-CM-6162-01A-11D-1650-10 | TCGA-CM-6162-10A-01D-1650-10 | g.chr16:27480708G>A | c.4978C>T | c.(4978-4980)Cgc>Tgc | p.R1660C |
| COADREAD | 16 | 27481682 | 27481682 | + | Missense_Mutation | SNP | T | T | C | TCGA-G4-6588-01A-11D-1771-10 | TCGA-G4-6588-10A-01D-1771-10 | g.chr16:27481682T>C | c.4561A>G | c.(4561-4563)Acg>Gcg | p.T1521A |
| COADREAD | 16 | 27483106 | 27483106 | + | Missense_Mutation | SNP | C | C | T | TCGA-A6-6653-01A-11D-1771-10 | TCGA-A6-6653-10A-01D-1771-10 | g.chr16:27483106C>T | c.4489G>A | c.(4489-4491)Gtg>Atg | p.V1497M |
| COADREAD | 16 | 27483108 | 27483108 | + | Missense_Mutation | SNP | A | A | G | TCGA-CM-6674-01A-11D-1835-10 | TCGA-CM-6674-10A-01D-1835-10 | g.chr16:27483108A>G | c.4487T>C | c.(4486-4488)tTc>tCc | p.F1496S |
| COADREAD | 16 | 27483197 | 27483197 | + | Missense_Mutation | SNP | C | C | A | TCGA-A6-3809-01A-01W-0995-10 | TCGA-A6-3809-11A-01W-0995-10 | g.chr16:27483197C>A | c.4398G>T | c.(4396-4398)aaG>aaT | p.K1466N |
| COADREAD | 16 | 27492404 | 27492404 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3870-01A-01W-0995-10 | TCGA-AA-3870-10A-01W-0995-10 | g.chr16:27492404C>T | c.4192G>A | c.(4192-4194)Gcc>Acc | p.A1398T |
| COADREAD | 16 | 27492455 | 27492455 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-3864-01A-01W-0995-10 | TCGA-AA-3864-10A-01W-0995-10 | g.chr16:27492455C>T | c.4141G>A | c.(4141-4143)Gcc>Acc | p.A1381T |
| COADREAD | 16 | 27495566 | 27495566 | + | Missense_Mutation | SNP | T | T | G | TCGA-AA-3561-01A-01W-0831-10 | TCGA-AA-3561-10A-01W-0831-10 | g.chr16:27495566T>G | c.3967A>C | c.(3967-3969)Ata>Cta | p.I1323L |
| COADREAD | 16 | 27497443 | 27497443 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3949-01A-01W-0995-10 | TCGA-AA-3949-10A-01W-0995-10 | g.chr16:27497443G>A | c.3733C>T | c.(3733-3735)Cgc>Tgc | p.R1245C |
| COADREAD | 16 | 27499588 | 27499588 | + | Silent | SNP | C | C | T | TCGA-AZ-4682-01B-01D-1408-10 | TCGA-AZ-4682-10A-01D-1408-10 | g.chr16:27499588C>T | c.3660G>A | c.(3658-3660)ctG>ctA | p.L1220L |
| COADREAD | 16 | 27499589 | 27499589 | + | Missense_Mutation | SNP | A | A | G | TCGA-AY-5543-01A-01D-1650-10 | TCGA-AY-5543-10A-01D-1650-10 | g.chr16:27499589A>G | c.3659T>C | c.(3658-3660)cTg>cCg | p.L1220P |
| COADREAD | 16 | 27499589 | 27499589 | + | Missense_Mutation | SNP | A | A | G | TCGA-F5-6702-01A-11D-1826-10 | TCGA-F5-6702-10A-01D-1826-10 | g.chr16:27499589A>G | c.3659T>C | c.(3658-3660)cTg>cCg | p.L1220P |
| COADREAD | 16 | 27500950 | 27500950 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-6928-01A-11D-1924-10 | TCGA-D5-6928-10A-01D-1924-10 | g.chr16:27500950C>T | c.3266G>A | c.(3265-3267)cGc>cAc | p.R1089H |
| COADREAD | 16 | 27503681 | 27503681 | + | Silent | SNP | G | G | A | TCGA-AA-3672-01A-01W-0900-09 | TCGA-AA-3672-10A-01W-0900-09 | g.chr16:27503681G>A | c.3129C>T | c.(3127-3129)tgC>tgT | p.C1043C |
| COADREAD | 16 | 27506767 | 27506767 | + | Silent | SNP | G | G | A | TCGA-CK-6746-01A-11D-1835-10 | TCGA-CK-6746-10A-01D-1835-10 | g.chr16:27506767G>A | c.2397C>T | c.(2395-2397)cgC>cgT | p.R799R |
| COADREAD | 16 | 27509009 | 27509009 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-A6-3809-01A-01W-0995-10 | TCGA-A6-3809-11A-01W-0995-10 | g.chr16:27509009delT | c.2299delA | c.(2299-2301)agtfs | p.S767fs |
| COADREAD | 16 | 27509009 | 27509009 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-AD-5900-01A-11D-1650-10 | TCGA-AD-5900-10A-01D-1650-10 | g.chr16:27509009delT | c.2299delA | c.(2299-2301)agtfs | p.S767fs |
| COADREAD | 16 | 27509009 | 27509009 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-CK-5916-01A-11D-1650-10 | TCGA-CK-5916-10A-01D-1650-10 | g.chr16:27509009delT | c.2299delA | c.(2299-2301)agtfs | p.S767fs |
| COADREAD | 16 | 27509009 | 27509009 | + | Frame_Shift_Del | DEL | T | T | - | TCGA-F4-6570-01A-11D-1771-10 | TCGA-F4-6570-10A-01D-1771-10 | g.chr16:27509009delT | c.2299delA | c.(2299-2301)agtfs | p.S767fs |
| COADREAD | 16 | 27509054 | 27509055 | + | Frame_Shift_Del | DEL | GA | GA | - | TCGA-AA-3713-01A-21D-1719-10 | TCGA-AA-3713-11A-01D-1719-10 | g.chr16:27509054_27509055delGA | c.2253_2254delTC | c.(2251-2256)tctcagfs | p.Q752fs |
| COADREAD | 16 | 27509109 | 27509109 | + | Silent | SNP | C | C | T | TCGA-F5-6813-01A-11D-1826-10 | TCGA-F5-6813-10A-01D-1826-10 | g.chr16:27509109C>T | c.2199G>A | c.(2197-2199)ggG>ggA | p.G733G |
| COADREAD | 16 | 27509111 | 27509111 | + | Missense_Mutation | SNP | C | C | A | TCGA-CM-6680-01A-11D-1835-10 | TCGA-CM-6680-10A-01D-1835-10 | g.chr16:27509111C>A | c.2197G>T | c.(2197-2199)Ggg>Tgg | p.G733W |
| COADREAD | 16 | 27509117 | 27509117 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-A010-01A-01W-A00E-09 | TCGA-AA-A010-10A-01W-A00E-09 | g.chr16:27509117G>A | c.2191C>T | c.(2191-2193)Ccc>Tcc | p.P731S |
| COADREAD | 16 | 27512525 | 27512525 | + | Missense_Mutation | SNP | C | C | T | TCGA-AF-2693-01A-02D-1733-10 | TCGA-AF-2693-10A-01D-1733-10 | g.chr16:27512525C>T | c.2048G>A | c.(2047-2049)gGc>gAc | p.G683D |
| COADREAD | 16 | 27512529 | 27512529 | + | Missense_Mutation | SNP | C | C | A | TCGA-G4-6628-01A-11D-1835-10 | TCGA-G4-6628-10A-01D-1835-10 | g.chr16:27512529C>A | c.2044G>T | c.(2044-2046)Gat>Tat | p.D682Y |
| COADREAD | 16 | 27512546 | 27512546 | + | Missense_Mutation | SNP | C | C | T | TCGA-A6-5665-01A-01D-1650-10 | TCGA-A6-5665-10A-01D-1650-10 | g.chr16:27512546C>T | c.2027G>A | c.(2026-2028)cGg>cAg | p.R676Q |
| COADREAD | 16 | 27514180 | 27514180 | + | Splice_Site | SNP | G | G | A | TCGA-CM-6171-01A-11D-1650-10 | TCGA-CM-6171-10A-01D-1650-10 | g.chr16:27514180G>A | c.1907C>T | c.(1906-1908)aCg>aTg | p.T636M |
| COADREAD | 16 | 27517276 | 27517276 | + | Missense_Mutation | SNP | C | C | T | TCGA-AA-A00A-01A-01W-A005-10 | TCGA-AA-A00A-10A-01W-A005-10 | g.chr16:27517276C>T | c.1714G>A | c.(1714-1716)Gac>Aac | p.D572N |
| COADREAD | 16 | 27517363 | 27517364 | + | Frame_Shift_Del | DEL | CT | CT | - | TCGA-AA-3672-01A-01W-0900-09 | TCGA-AA-3672-10A-01W-0900-09 | g.chr16:27517363_27517364delCT | c.1626_1627delAG | c.(1624-1629)agagccfs | p.RA542fs |
| COADREAD | 16 | 27518173 | 27518173 | + | Missense_Mutation | SNP | G | G | C | TCGA-AA-3663-01A-01D-1719-10 | TCGA-AA-3663-11A-01D-1719-10 | g.chr16:27518173G>C | c.1547C>G | c.(1546-1548)aCc>aGc | p.T516S |
| COADREAD | 16 | 27523104 | 27523104 | + | Silent | SNP | G | G | A | TCGA-AA-3510-01A-01D-1408-10 | TCGA-AA-3510-11A-01D-1408-10 | g.chr16:27523104G>A | c.1092C>T | c.(1090-1092)ttC>ttT | p.F364F |
| COADREAD | 16 | 27523175 | 27523175 | + | Missense_Mutation | SNP | G | G | A | TCGA-A6-6653-01A-11D-1771-10 | TCGA-A6-6653-10A-01D-1771-10 | g.chr16:27523175G>A | c.1021C>T | c.(1021-1023)Cgg>Tgg | p.R341W |
| COADREAD | 16 | 27549526 | 27549526 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-AG-A020-01A-21W-A096-10 | TCGA-AG-A020-11A-11W-A096-10 | g.chr16:27549526G>A | c.583C>T | c.(583-585)Cga>Tga | p.R195* |
| COADREAD | 16 | 27556754 | 27556754 | + | Silent | SNP | T | T | C | TCGA-AA-A022-01A-21W-A096-10 | TCGA-AA-A022-11A-11W-A096-10 | g.chr16:27556754T>C | c.312A>G | c.(310-312)ttA>ttG | p.L104L |
| COADREAD | 16 | 27556783 | 27556783 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-D5-6540-01A-11D-1719-10 | TCGA-D5-6540-10A-01D-1719-10 | g.chr16:27556783C>A | c.283G>T | c.(283-285)Gag>Tag | p.E95* |
| DLBC | 16 | 27499956 | 27499956 | + | Splice_Site | DEL | C | C | - | TCGA-G8-6909-01A-11D-2210-10 | TCGA-G8-6909-14A-01D-2210-10 | g.chr16:27499956delC | c.3430delG | c.(3430-3432)gag>ag | p.E1144fs |
| ESCA | 16 | 27475803 | 27475803 | + | Missense_Mutation | SNP | C | C | T | TCGA-IG-A5B8-01A-11D-A28B-09 | TCGA-IG-A5B8-10A-01D-A28E-09 | g.chr16:27475803C>T | c.5710G>A | c.(5710-5712)Ggg>Agg | p.G1904R |
| ESCA | 16 | 27475971 | 27475972 | + | Frame_Shift_Ins | INS | - | - | G | TCGA-L5-A43J-01A-12D-A247-09 | TCGA-L5-A43J-11A-11D-A247-09 | g.chr16:27475971_27475972insG | c.5541_5542insC | c.(5539-5544)cccgagfs | p.E1848fs |
| ESCA | 16 | 27481557 | 27481557 | + | Silent | SNP | G | G | A | TCGA-LN-A4MR-01A-11D-A28B-09 | TCGA-LN-A4MR-10A-01D-A28E-09 | g.chr16:27481557G>A | c.4686C>T | c.(4684-4686)gaC>gaT | p.D1562D |
| ESCA | 16 | 27495595 | 27495595 | + | Missense_Mutation | SNP | G | G | A | TCGA-RE-A7BO-01A-11D-A33E-09 | TCGA-RE-A7BO-10A-01D-A33H-09 | g.chr16:27495595G>A | c.3938C>T | c.(3937-3939)tCt>tTt | p.S1313F |
| ESCA | 16 | 27506096 | 27506096 | + | Missense_Mutation | SNP | T | T | A | TCGA-L5-A43J-01A-12D-A247-09 | TCGA-L5-A43J-11A-11D-A247-09 | g.chr16:27506096T>A | c.2766A>T | c.(2764-2766)caA>caT | p.Q922H |
| ESCA | 16 | 27549607 | 27549607 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-L5-A8NM-01A-11D-A37C-09 | TCGA-L5-A8NM-11A-12D-A37F-09 | g.chr16:27549607delC | c.502delG | c.(502-504)gatfs | p.D168fs |
| GBM | 16 | 27480738 | 27480738 | + | Missense_Mutation | SNP | C | C | T | TCGA-28-2510-01A-01D-1696-08 | TCGA-28-2510-10A-01D-1696-08 | g.chr16:27480738C>T | c.4948G>A | c.(4948-4950)Ggc>Agc | p.G1650S |
| GBM | 16 | 27483187 | 27483187 | + | Missense_Mutation | SNP | C | C | G | TCGA-06-0745-01A-01W-0348-08 | TCGA-06-0745-10A-01W-0348-08 | g.chr16:27483187C>G | c.4408G>C | c.(4408-4410)Gag>Cag | p.E1470Q |
| GBM | 16 | 27499713 | 27499713 | + | Missense_Mutation | SNP | C | C | G | TCGA-28-5219-01A-01D-1486-08 | TCGA-28-5219-10A-01D-1486-08 | g.chr16:27499713C>G | c.3535G>C | c.(3535-3537)Ggg>Cgg | p.G1179R |
| GBM | 16 | 27518426 | 27518426 | + | Missense_Mutation | SNP | C | C | T | TCGA-06-0174-01A-01D-1491-08 | TCGA-06-0174-10B-01D-1491-08 | g.chr16:27518426C>T | c.1294G>A | c.(1294-1296)Gtg>Atg | p.V432M |
| GBMLGG | 16 | 27472858 | 27472858 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr16:27472858C>T | c.6143G>A | c.(6142-6144)cGg>cAg | p.R2048Q |
| GBMLGG | 16 | 27480738 | 27480738 | + | Missense_Mutation | SNP | C | C | T | TCGA-28-2510-01A-01D-1696-08 | TCGA-28-2510-10A-01D-1696-08 | g.chr16:27480738C>T | c.4948G>A | c.(4948-4950)Ggc>Agc | p.G1650S |
| GBMLGG | 16 | 27480831 | 27480831 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr16:27480831C>A | c.4855G>T | c.(4855-4857)Gag>Tag | p.E1619* |
| GBMLGG | 16 | 27483187 | 27483187 | + | Missense_Mutation | SNP | C | C | G | TCGA-06-0745-01A-01W-0348-08 | TCGA-06-0745-10A-01W-0348-08 | g.chr16:27483187C>G | c.4408G>C | c.(4408-4410)Gag>Cag | p.E1470Q |
| GBMLGG | 16 | 27499713 | 27499713 | + | Missense_Mutation | SNP | C | C | G | TCGA-28-5219-01A-01D-1486-08 | TCGA-28-5219-10A-01D-1486-08 | g.chr16:27499713C>G | c.3535G>C | c.(3535-3537)Ggg>Cgg | p.G1179R |
| GBMLGG | 16 | 27503732 | 27503733 | + | Frame_Shift_Del | DEL | AT | AT | - | TCGA-DU-A6S8-01A-12D-A32B-08 | TCGA-DU-A6S8-10A-01D-A329-08 | g.chr16:27503732_27503733delAT | c.3077_3078delAT | c.(3076-3078)tatfs | p.Y1026fs |
| GBMLGG | 16 | 27503949 | 27503949 | + | Missense_Mutation | SNP | C | C | G | TCGA-TM-A7C4-01A-11D-A32B-08 | TCGA-TM-A7C4-10A-01D-A329-08 | g.chr16:27503949C>G | c.2962G>C | c.(2962-2964)Gat>Cat | p.D988H |
| GBMLGG | 16 | 27504543 | 27504543 | + | Silent | SNP | A | A | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr16:27504543A>G | c.2853T>C | c.(2851-2853)atT>atC | p.I951I |
| GBMLGG | 16 | 27508992 | 27508992 | + | Silent | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr16:27508992G>A | c.2316C>T | c.(2314-2316)ggC>ggT | p.G772G |
| GBMLGG | 16 | 27510034 | 27510034 | + | Silent | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr16:27510034C>T | c.2082G>A | c.(2080-2082)ccG>ccA | p.P694P |
| GBMLGG | 16 | 27518325 | 27518325 | + | Silent | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr16:27518325C>T | c.1395G>A | c.(1393-1395)tcG>tcA | p.S465S |
| GBMLGG | 16 | 27518347 | 27518347 | + | Missense_Mutation | SNP | A | A | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr16:27518347A>G | c.1373T>C | c.(1372-1374)cTg>cCg | p.L458P |
| GBMLGG | 16 | 27518426 | 27518426 | + | Missense_Mutation | SNP | C | C | T | TCGA-06-0174-01A-01D-1491-08 | TCGA-06-0174-10B-01D-1491-08 | g.chr16:27518426C>T | c.1294G>A | c.(1294-1296)Gtg>Atg | p.V432M |
| GBMLGG | 16 | 27544670 | 27544670 | + | Missense_Mutation | SNP | A | A | C | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr16:27544670A>C | c.791T>G | c.(790-792)gTc>gGc | p.V264G |
| GBMLGG | 16 | 27544702 | 27544702 | + | Missense_Mutation | SNP | G | G | C | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr16:27544702G>C | c.759C>G | c.(757-759)agC>agG | p.S253R |
| HNSC | 16 | 27472687 | 27472687 | + | Missense_Mutation | SNP | T | T | C | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr16:27472687T>C | c.6314A>G | c.(6313-6315)aAg>aGg | p.K2105R |
| HNSC | 16 | 27472703 | 27472703 | + | Missense_Mutation | SNP | C | C | T | TCGA-CN-6023-01A-11D-1683-08 | TCGA-CN-6023-10A-01D-1683-08 | g.chr16:27472703C>T | c.6298G>A | c.(6298-6300)Gag>Aag | p.E2100K |
| HNSC | 16 | 27475887 | 27475887 | + | Missense_Mutation | SNP | C | C | T | TCGA-P3-A6T4-01A-11D-A34J-08 | TCGA-P3-A6T4-10A-01D-A34M-08 | g.chr16:27475887C>T | c.5626G>A | c.(5626-5628)Gag>Aag | p.E1876K |
| HNSC | 16 | 27476027 | 27476027 | + | Missense_Mutation | SNP | C | C | G | TCGA-CV-7435-01A-11D-2129-08 | TCGA-CV-7435-10A-01D-2129-08 | g.chr16:27476027C>G | c.5486G>C | c.(5485-5487)aGa>aCa | p.R1829T |
| HNSC | 16 | 27476145 | 27476145 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-CR-6491-01A-11D-1870-08 | TCGA-CR-6491-10A-01D-1870-08 | g.chr16:27476145G>A | c.5368C>T | c.(5368-5370)Cag>Tag | p.Q1790* |
| HNSC | 16 | 27480660 | 27480660 | + | Missense_Mutation | SNP | T | T | C | TCGA-F7-A624-01A-22D-A30E-08 | TCGA-F7-A624-10A-01D-A30H-08 | g.chr16:27480660T>C | c.5026A>G | c.(5026-5028)Aag>Gag | p.K1676E |
| HNSC | 16 | 27480793 | 27480793 | + | Silent | SNP | C | C | G | TCGA-CR-5248-01A-01D-2012-08 | TCGA-CR-5248-10A-01D-2013-08 | g.chr16:27480793C>G | c.4893G>C | c.(4891-4893)cgG>cgC | p.R1631R |
| HNSC | 16 | 27480820 | 27480820 | + | Missense_Mutation | SNP | C | C | G | TCGA-MZ-A7D7-01A-21D-A34J-08 | TCGA-MZ-A7D7-10A-01D-A34M-08 | g.chr16:27480820C>G | c.4866G>C | c.(4864-4866)ttG>ttC | p.L1622F |
| HNSC | 16 | 27483198 | 27483198 | + | Missense_Mutation | SNP | T | T | C | TCGA-BA-6870-01A-11D-1870-08 | TCGA-BA-6870-10A-01D-1870-08 | g.chr16:27483198T>C | c.4397A>G | c.(4396-4398)aAg>aGg | p.K1466R |
| HNSC | 16 | 27495572 | 27495572 | + | Missense_Mutation | SNP | G | G | A | TCGA-CR-6481-01A-11D-1870-08 | TCGA-CR-6481-10A-01D-1870-08 | g.chr16:27495572G>A | c.3961C>T | c.(3961-3963)Cgc>Tgc | p.R1321C |
| HNSC | 16 | 27504019 | 27504019 | + | Silent | SNP | C | C | T | TCGA-CV-7183-01A-11D-2012-08 | TCGA-CV-7183-10A-01D-2013-08 | g.chr16:27504019C>T | c.2892G>A | c.(2890-2892)tcG>tcA | p.S964S |
| HNSC | 16 | 27514201 | 27514201 | + | Missense_Mutation | SNP | C | C | G | TCGA-CV-A45W-01A-11D-A25D-08 | TCGA-CV-A45W-10A-01D-A25E-08 | g.chr16:27514201C>G | c.1886G>C | c.(1885-1887)cGc>cCc | p.R629P |
| HNSC | 16 | 27518206 | 27518206 | + | Missense_Mutation | SNP | C | C | T | TCGA-BA-A6DB-01A-11D-A30E-08 | TCGA-BA-A6DB-10A-01D-A30H-08 | g.chr16:27518206C>T | c.1514G>A | c.(1513-1515)cGg>cAg | p.R505Q |
| HNSC | 16 | 27539953 | 27539953 | + | Silent | SNP | G | G | A | TCGA-CN-5369-01A-01D-1434-08 | TCGA-CN-5369-10A-01D-1434-08 | g.chr16:27539953G>A | c.939C>T | c.(937-939)atC>atT | p.I313I |
| HNSC | 16 | 27544670 | 27544670 | + | Missense_Mutation | SNP | A | A | T | TCGA-CV-7263-01A-11D-2012-08 | TCGA-CV-7263-10A-01D-2013-08 | g.chr16:27544670A>T | c.791T>A | c.(790-792)gTc>gAc | p.V264D |
| HNSC | 16 | 27549199 | 27549199 | + | Missense_Mutation | SNP | C | C | T | TCGA-UF-A71D-01A-12D-A34J-08 | TCGA-UF-A71D-10B-01D-A34M-08 | g.chr16:27549199C>T | c.658G>A | c.(658-660)Ggg>Agg | p.G220R |
| HNSC | 16 | 27549582 | 27549582 | + | Missense_Mutation | SNP | A | A | T | TCGA-CR-7367-01A-11D-2012-08 | TCGA-CR-7367-10A-01D-2013-08 | g.chr16:27549582A>T | c.527T>A | c.(526-528)tTc>tAc | p.F176Y |
| HNSC | 16 | 27556684 | 27556684 | + | Missense_Mutation | SNP | T | T | C | TCGA-CN-5360-01A-01D-1434-08 | TCGA-CN-5360-10A-01D-1434-08 | g.chr16:27556684T>C | c.382A>G | c.(382-384)Aga>Gga | p.R128G |
| HNSC | 16 | 27561047 | 27561047 | + | Silent | SNP | C | C | T | TCGA-CN-6996-01A-11D-1912-08 | TCGA-CN-6996-10A-01D-1912-08 | g.chr16:27561047C>T | c.165G>A | c.(163-165)ccG>ccA | p.P55P |
| HNSC | 16 | 27561184 | 27561184 | + | Missense_Mutation | SNP | C | C | G | TCGA-CR-7388-01A-11D-2012-08 | TCGA-CR-7388-10A-01D-2013-08 | g.chr16:27561184C>G | c.28G>C | c.(28-30)Gaa>Caa | p.E10Q |
| KIPAN | 16 | 27480845 | 27480845 | + | Missense_Mutation | SNP | T | T | C | TCGA-MH-A854-01A-11D-A34Z-10 | TCGA-MH-A854-10A-01D-A34Z-10 | g.chr16:27480845T>C | c.4841A>G | c.(4840-4842)gAt>gGt | p.D1614G |
| KIPAN | 16 | 27481696 | 27481696 | + | Missense_Mutation | SNP | G | G | A | TCGA-A3-3322-01A-01W-0886-08 | TCGA-A3-3322-11A-01D-0966-08 | g.chr16:27481696G>A | c.4547C>T | c.(4546-4548)cCa>cTa | p.P1516L |
| KIPAN | 16 | 27497454 | 27497454 | + | Missense_Mutation | SNP | C | C | A | TCGA-A3-3326-01A-01D-0966-08 | TCGA-A3-3326-11A-01D-0966-08 | g.chr16:27497454C>A | c.3722G>T | c.(3721-3723)aGc>aTc | p.S1241I |
| KIPAN | 16 | 27500985 | 27500986 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-BP-5168-01A-01D-1421-08 | TCGA-BP-5168-11A-01D-1421-08 | g.chr16:27500985_27500986insT | c.3230_3231insA | c.(3229-3231)gagfs | p.E1077fs |
| KIPAN | 16 | 27504025 | 27504025 | + | Missense_Mutation | SNP | A | A | C | TCGA-CZ-5985-01A-11D-1669-08 | TCGA-CZ-5985-11A-01D-1669-08 | g.chr16:27504025A>C | c.2886T>G | c.(2884-2886)atT>atG | p.I962M |
| KIPAN | 16 | 27504602 | 27504602 | + | Missense_Mutation | SNP | C | C | T | TCGA-CJ-4874-01A-01D-1373-10 | TCGA-CJ-4874-11A-01D-1373-10 | g.chr16:27504602C>T | c.2794G>A | c.(2794-2796)Gaa>Aaa | p.E932K |
| KIPAN | 16 | 27519910 | 27519910 | + | Missense_Mutation | SNP | A | A | G | TCGA-DW-7841-01A-11D-2136-08 | TCGA-DW-7841-10A-01D-2136-08 | g.chr16:27519910A>G | c.1193T>C | c.(1192-1194)cTa>cCa | p.L398P |
| KIPAN | 16 | 27523094 | 27523094 | + | Missense_Mutation | SNP | T | T | C | TCGA-2Z-A9JG-01A-11D-A42J-10 | TCGA-2Z-A9JG-10A-01D-A42M-10 | g.chr16:27523094T>C | c.1102A>G | c.(1102-1104)Atg>Gtg | p.M368V |
| KIPAN | 16 | 27523128 | 27523128 | + | Silent | SNP | T | T | C | TCGA-BP-5198-01A-01D-1429-08 | TCGA-BP-5198-11A-01D-1429-08 | g.chr16:27523128T>C | c.1068A>G | c.(1066-1068)acA>acG | p.T356T |
| KIPAN | 16 | 27523215 | 27523215 | + | Silent | SNP | G | G | A | TCGA-B8-5162-01A-01D-1421-08 | TCGA-B8-5162-10A-01D-1421-08 | g.chr16:27523215G>A | c.981C>T | c.(979-981)gaC>gaT | p.D327D |
| KIPAN | 16 | 27549611 | 27549611 | + | Silent | SNP | C | C | T | TCGA-B9-A69E-01A-11D-A31X-10 | TCGA-B9-A69E-10A-01D-A31X-10 | g.chr16:27549611C>T | c.498G>A | c.(496-498)gaG>gaA | p.E166E |
| KIPAN | 16 | 27561107 | 27561108 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-A4-A7UZ-01A-12D-A34Z-10 | TCGA-A4-A7UZ-10A-01D-A34Z-10 | g.chr16:27561107_27561108insA | c.104_105insT | c.(103-105)ttcfs | p.F35fs |
| KIRC | 16 | 27481696 | 27481696 | + | Missense_Mutation | SNP | G | G | A | TCGA-A3-3322-01A-01W-0886-08 | TCGA-A3-3322-11A-01D-0966-08 | g.chr16:27481696G>A | c.4547C>T | c.(4546-4548)cCa>cTa | p.P1516L |
| KIRC | 16 | 27497454 | 27497454 | + | Missense_Mutation | SNP | C | C | A | TCGA-A3-3326-01A-01D-0966-08 | TCGA-A3-3326-11A-01D-0966-08 | g.chr16:27497454C>A | c.3722G>T | c.(3721-3723)aGc>aTc | p.S1241I |
| KIRC | 16 | 27500985 | 27500986 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-BP-5168-01A-01D-1421-08 | TCGA-BP-5168-11A-01D-1421-08 | g.chr16:27500985_27500986insT | c.3230_3231insA | c.(3229-3231)gagfs | p.E1077fs |
| KIRC | 16 | 27504025 | 27504025 | + | Missense_Mutation | SNP | A | A | C | TCGA-CZ-5985-01A-11D-1669-08 | TCGA-CZ-5985-11A-01D-1669-08 | g.chr16:27504025A>C | c.2886T>G | c.(2884-2886)atT>atG | p.I962M |
| KIRC | 16 | 27504602 | 27504602 | + | Missense_Mutation | SNP | C | C | T | TCGA-CJ-4874-01A-01D-1373-10 | TCGA-CJ-4874-11A-01D-1373-10 | g.chr16:27504602C>T | c.2794G>A | c.(2794-2796)Gaa>Aaa | p.E932K |
| KIRC | 16 | 27523128 | 27523128 | + | Silent | SNP | T | T | C | TCGA-BP-5198-01A-01D-1429-08 | TCGA-BP-5198-11A-01D-1429-08 | g.chr16:27523128T>C | c.1068A>G | c.(1066-1068)acA>acG | p.T356T |
| KIRC | 16 | 27523215 | 27523215 | + | Silent | SNP | G | G | A | TCGA-B8-5162-01A-01D-1421-08 | TCGA-B8-5162-10A-01D-1421-08 | g.chr16:27523215G>A | c.981C>T | c.(979-981)gaC>gaT | p.D327D |
| KIRP | 16 | 27480845 | 27480845 | + | Missense_Mutation | SNP | T | T | C | TCGA-MH-A854-01A-11D-A34Z-10 | TCGA-MH-A854-10A-01D-A34Z-10 | g.chr16:27480845T>C | c.4841A>G | c.(4840-4842)gAt>gGt | p.D1614G |
| KIRP | 16 | 27519910 | 27519910 | + | Missense_Mutation | SNP | A | A | G | TCGA-DW-7841-01A-11D-2136-08 | TCGA-DW-7841-10A-01D-2136-08 | g.chr16:27519910A>G | c.1193T>C | c.(1192-1194)cTa>cCa | p.L398P |
| KIRP | 16 | 27523094 | 27523094 | + | Missense_Mutation | SNP | T | T | C | TCGA-2Z-A9JG-01A-11D-A42J-10 | TCGA-2Z-A9JG-10A-01D-A42M-10 | g.chr16:27523094T>C | c.1102A>G | c.(1102-1104)Atg>Gtg | p.M368V |
| KIRP | 16 | 27549611 | 27549611 | + | Silent | SNP | C | C | T | TCGA-B9-A69E-01A-11D-A31X-10 | TCGA-B9-A69E-10A-01D-A31X-10 | g.chr16:27549611C>T | c.498G>A | c.(496-498)gaG>gaA | p.E166E |
| KIRP | 16 | 27561107 | 27561108 | + | Frame_Shift_Ins | INS | - | - | A | TCGA-A4-A7UZ-01A-12D-A34Z-10 | TCGA-A4-A7UZ-10A-01D-A34Z-10 | g.chr16:27561107_27561108insA | c.104_105insT | c.(103-105)ttcfs | p.F35fs |
| LGG | 16 | 27472858 | 27472858 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr16:27472858C>T | c.6143G>A | c.(6142-6144)cGg>cAg | p.R2048Q |
| LGG | 16 | 27480831 | 27480831 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr16:27480831C>A | c.4855G>T | c.(4855-4857)Gag>Tag | p.E1619* |
| LGG | 16 | 27503732 | 27503733 | + | Frame_Shift_Del | DEL | AT | AT | - | TCGA-DU-A6S8-01A-12D-A32B-08 | TCGA-DU-A6S8-10A-01D-A329-08 | g.chr16:27503732_27503733delAT | c.3077_3078delAT | c.(3076-3078)tatfs | p.Y1026fs |
| LGG | 16 | 27503949 | 27503949 | + | Missense_Mutation | SNP | C | C | G | TCGA-TM-A7C4-01A-11D-A32B-08 | TCGA-TM-A7C4-10A-01D-A329-08 | g.chr16:27503949C>G | c.2962G>C | c.(2962-2964)Gat>Cat | p.D988H |
| LGG | 16 | 27504543 | 27504543 | + | Silent | SNP | A | A | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr16:27504543A>G | c.2853T>C | c.(2851-2853)atT>atC | p.I951I |
| LGG | 16 | 27508992 | 27508992 | + | Silent | SNP | G | G | A | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr16:27508992G>A | c.2316C>T | c.(2314-2316)ggC>ggT | p.G772G |
| LGG | 16 | 27510034 | 27510034 | + | Silent | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr16:27510034C>T | c.2082G>A | c.(2080-2082)ccG>ccA | p.P694P |
| LGG | 16 | 27518325 | 27518325 | + | Silent | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr16:27518325C>T | c.1395G>A | c.(1393-1395)tcG>tcA | p.S465S |
| LGG | 16 | 27518347 | 27518347 | + | Missense_Mutation | SNP | A | A | G | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr16:27518347A>G | c.1373T>C | c.(1372-1374)cTg>cCg | p.L458P |
| LGG | 16 | 27544670 | 27544670 | + | Missense_Mutation | SNP | A | A | C | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr16:27544670A>C | c.791T>G | c.(790-792)gTc>gGc | p.V264G |
| LGG | 16 | 27544702 | 27544702 | + | Missense_Mutation | SNP | G | G | C | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr16:27544702G>C | c.759C>G | c.(757-759)agC>agG | p.S253R |
| LIHC | 16 | 27472839 | 27472839 | + | Missense_Mutation | SNP | C | C | A | TCGA-CC-A7IH-01A-11D-A33K-10 | TCGA-CC-A7IH-10A-01D-A33K-10 | g.chr16:27472839C>A | c.6162G>T | c.(6160-6162)aaG>aaT | p.K2054N |
| LIHC | 16 | 27499733 | 27499733 | + | Missense_Mutation | SNP | T | T | C | TCGA-ES-A2HS-01A-11D-A183-10 | TCGA-ES-A2HS-11A-11D-A183-10 | g.chr16:27499733T>C | c.3515A>G | c.(3514-3516)aAc>aGc | p.N1172S |
| LIHC | 16 | 27503691 | 27503691 | + | Missense_Mutation | SNP | T | T | C | TCGA-DD-A3A0-01A-11D-A20W-10 | TCGA-DD-A3A0-11A-11D-A20W-10 | g.chr16:27503691T>C | c.3119A>G | c.(3118-3120)gAc>gGc | p.D1040G |
| LIHC | 16 | 27506736 | 27506736 | + | Missense_Mutation | SNP | G | G | T | TCGA-EP-A2KB-01A-11D-A183-10 | TCGA-EP-A2KB-10A-01D-A183-10 | g.chr16:27506736G>T | c.2428C>A | c.(2428-2430)Ctc>Atc | p.L810I |
| LIHC | 16 | 27509073 | 27509073 | + | Silent | SNP | T | T | C | TCGA-UB-A7MB-01A-11D-A33Q-10 | TCGA-UB-A7MB-10A-01D-A33Q-10 | g.chr16:27509073T>C | c.2235A>G | c.(2233-2235)ccA>ccG | p.P745P |
| LIHC | 16 | 27517278 | 27517278 | + | Missense_Mutation | SNP | G | G | T | TCGA-DD-A115-01A-11D-A12Z-10 | TCGA-DD-A115-10A-01D-A12Z-10 | g.chr16:27517278G>T | c.1712C>A | c.(1711-1713)gCg>gAg | p.A571E |
| LIHC | 16 | 27517278 | 27517278 | + | Missense_Mutation | SNP | G | G | T | TCGA-DD-A1EE-01A-11D-A12Z-10 | TCGA-DD-A1EE-10A-01D-A12Z-10 | g.chr16:27517278G>T | c.1712C>A | c.(1711-1713)gCg>gAg | p.A571E |
| LIHC | 16 | 27549250 | 27549250 | + | Splice_Site | SNP | T | T | A | TCGA-NI-A4U2-01A-11D-A28X-10 | TCGA-NI-A4U2-10A-01D-A28X-10 | g.chr16:27549250T>A | | c.e4-2 | |
| LIHC | 16 | 27549677 | 27549677 | + | Splice_Site | SNP | C | C | A | TCGA-2Y-A9GZ-01A-11D-A38X-10 | TCGA-2Y-A9GZ-10A-01D-A38X-10 | g.chr16:27549677C>A | c.432G>T | c.(430-432)agG>agT | p.R144S |
| LUAD | 16 | 27472818 | 27472818 | + | Silent | SNP | G | G | A | TCGA-75-6214-01A-41D-1945-08 | TCGA-75-6214-10A-01D-1946-08 | g.chr16:27472818G>A | c.6183C>T | c.(6181-6183)ttC>ttT | p.F2061F |
| LUAD | 16 | 27473778 | 27473778 | + | Missense_Mutation | SNP | C | C | A | TCGA-97-7938-01A-11D-2167-08 | TCGA-97-7938-10A-01D-2167-08 | g.chr16:27473778C>A | c.5954G>T | c.(5953-5955)cGg>cTg | p.R1985L |
| LUAD | 16 | 27475683 | 27475683 | + | Missense_Mutation | SNP | T | T | G | TCGA-17-Z056-01A-01W-0747-08 | TCGA-17-Z056-11A-01W-0747-08 | g.chr16:27475683T>G | c.5830A>C | c.(5830-5832)Agc>Cgc | p.S1944R |
| LUAD | 16 | 27475738 | 27475738 | + | Silent | SNP | T | T | C | TCGA-55-6968-01A-11D-1945-08 | TCGA-55-6968-11A-01D-1945-08 | g.chr16:27475738T>C | c.5775A>G | c.(5773-5775)gcA>gcG | p.A1925A |
| LUAD | 16 | 27475845 | 27475845 | + | Missense_Mutation | SNP | C | C | A | TCGA-44-8117-01A-11D-2238-08 | TCGA-44-8117-10A-01D-2238-08 | g.chr16:27475845C>A | c.5668G>T | c.(5668-5670)Gac>Tac | p.D1890Y |
| LUAD | 16 | 27475893 | 27475893 | + | Missense_Mutation | SNP | C | C | G | TCGA-53-A4EZ-01A-12D-A24P-08 | TCGA-53-A4EZ-10A-01D-A24P-08 | g.chr16:27475893C>G | c.5620G>C | c.(5620-5622)Gac>Cac | p.D1874H |
| LUAD | 16 | 27476020 | 27476020 | + | Missense_Mutation | SNP | G | G | T | TCGA-55-8511-01A-11D-2393-08 | TCGA-55-8511-10A-01D-2393-08 | g.chr16:27476020G>T | c.5493C>A | c.(5491-5493)gaC>gaA | p.D1831E |
| LUAD | 16 | 27476021 | 27476021 | + | Missense_Mutation | SNP | T | T | G | TCGA-55-8511-01A-11D-2393-08 | TCGA-55-8511-10A-01D-2393-08 | g.chr16:27476021T>G | c.5492A>C | c.(5491-5493)gAc>gCc | p.D1831A |
| LUAD | 16 | 27476052 | 27476052 | + | Missense_Mutation | SNP | C | C | G | TCGA-73-4659-01A-01D-1265-08 | TCGA-73-4659-11A-01D-1265-08 | g.chr16:27476052C>G | c.5461G>C | c.(5461-5463)Gac>Cac | p.D1821H |
| LUAD | 16 | 27476583 | 27476583 | + | Missense_Mutation | SNP | G | G | T | TCGA-78-7155-01A-11D-2036-08 | TCGA-78-7155-10A-01D-2036-08 | g.chr16:27476583G>T | c.5353C>A | c.(5353-5355)Cag>Aag | p.Q1785K |
| LUAD | 16 | 27476638 | 27476638 | + | Silent | SNP | G | G | A | TCGA-05-4382-01A-01D-1931-08 | TCGA-05-4382-10A-01D-1265-08 | g.chr16:27476638G>A | c.5298C>T | c.(5296-5298)ttC>ttT | p.F1766F |
| LUAD | 16 | 27476787 | 27476787 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-17-Z060-01A-01W-0747-08 | TCGA-17-Z060-11A-01W-0747-08 | g.chr16:27476787C>A | c.5149G>T | c.(5149-5151)Gaa>Taa | p.E1717* |
| LUAD | 16 | 27480738 | 27480738 | + | Missense_Mutation | SNP | C | C | A | TCGA-MN-A4N4-01A-12D-A24P-08 | TCGA-MN-A4N4-10A-01D-A24P-08 | g.chr16:27480738C>A | c.4948G>T | c.(4948-4950)Ggc>Tgc | p.G1650C |
| LUAD | 16 | 27480842 | 27480842 | + | Missense_Mutation | SNP | T | T | A | TCGA-95-7043-01A-11D-1945-08 | TCGA-95-7043-10A-01D-1946-08 | g.chr16:27480842T>A | c.4844A>T | c.(4843-4845)gAc>gTc | p.D1615V |
| LUAD | 16 | 27481437 | 27481437 | + | Silent | SNP | G | G | A | TCGA-86-A4JF-01A-11D-A24P-08 | TCGA-86-A4JF-10A-01D-A24P-08 | g.chr16:27481437G>A | c.4806C>T | c.(4804-4806)gtC>gtT | p.V1602V |
| LUAD | 16 | 27481533 | 27481533 | + | Silent | SNP | G | G | A | TCGA-97-8176-01A-11D-2393-08 | TCGA-97-8176-10B-01D-2393-08 | g.chr16:27481533G>A | c.4710C>T | c.(4708-4710)gcC>gcT | p.A1570A |
| LUAD | 16 | 27481580 | 27481580 | + | Missense_Mutation | SNP | C | C | T | TCGA-50-5936-01A-11D-1625-08 | TCGA-50-5936-11A-01D-1625-08 | g.chr16:27481580C>T | c.4663G>A | c.(4663-4665)Gac>Aac | p.D1555N |
| LUAD | 16 | 27481653 | 27481653 | + | Missense_Mutation | SNP | C | C | A | TCGA-55-8510-01A-11D-2393-08 | TCGA-55-8510-10A-01D-2393-08 | g.chr16:27481653C>A | c.4590G>T | c.(4588-4590)atG>atT | p.M1530I |
| LUAD | 16 | 27483125 | 27483125 | + | Silent | SNP | C | C | T | TCGA-75-5122-01A-01D-1753-08 | TCGA-75-5122-10A-01D-1753-08 | g.chr16:27483125C>T | c.4470G>A | c.(4468-4470)aaG>aaA | p.K1490K |
| LUAD | 16 | 27492447 | 27492447 | + | Silent | SNP | C | C | T | TCGA-38-4626-01A-01D-1553-08 | TCGA-38-4626-11A-01D-1553-08 | g.chr16:27492447C>T | c.4149G>A | c.(4147-4149)agG>agA | p.R1383R |
| LUAD | 16 | 27497373 | 27497373 | + | Missense_Mutation | SNP | T | T | A | TCGA-78-7155-01A-11D-2036-08 | TCGA-78-7155-10A-01D-2036-08 | g.chr16:27497373T>A | c.3803A>T | c.(3802-3804)cAg>cTg | p.Q1268L |
| LUAD | 16 | 27497397 | 27497397 | + | Missense_Mutation | SNP | C | C | A | TCGA-55-8510-01A-11D-2393-08 | TCGA-55-8510-10A-01D-2393-08 | g.chr16:27497397C>A | c.3779G>T | c.(3778-3780)cGg>cTg | p.R1260L |
| LUAD | 16 | 27497405 | 27497405 | + | Silent | SNP | C | C | A | TCGA-L4-A4E5-01A-11D-A24P-08 | TCGA-L4-A4E5-10A-01D-A24P-08 | g.chr16:27497405C>A | c.3771G>T | c.(3769-3771)cgG>cgT | p.R1257R |
| LUAD | 16 | 27497465 | 27497465 | + | Silent | SNP | T | T | A | TCGA-55-8301-01A-11D-2284-08 | TCGA-55-8301-10A-01D-2284-08 | g.chr16:27497465T>A | c.3711A>T | c.(3709-3711)ccA>ccT | p.P1237P |
| LUAD | 16 | 27499558 | 27499558 | + | Missense_Mutation | SNP | T | T | A | TCGA-64-5775-01A-01D-1625-08 | TCGA-64-5775-10A-01D-1625-08 | g.chr16:27499558T>A | c.3690A>T | c.(3688-3690)agA>agT | p.R1230S |
| LUAD | 16 | 27499675 | 27499675 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-78-7158-01A-11D-2036-08 | TCGA-78-7158-10A-01D-2036-08 | g.chr16:27499675C>T | c.3573G>A | c.(3571-3573)tgG>tgA | p.W1191* |
| LUAD | 16 | 27499680 | 27499680 | + | Missense_Mutation | SNP | C | C | A | TCGA-75-5126-01A-01D-1753-08 | TCGA-75-5126-10A-01D-1753-08 | g.chr16:27499680C>A | c.3568G>T | c.(3568-3570)Ggc>Tgc | p.G1190C |
| LUAD | 16 | 27499898 | 27499898 | + | Missense_Mutation | SNP | C | C | A | TCGA-NJ-A4YQ-01A-11D-A25L-08 | TCGA-NJ-A4YQ-10A-01D-A25L-08 | g.chr16:27499898C>A | c.3488G>T | c.(3487-3489)cGc>cTc | p.R1163L |
| LUAD | 16 | 27500985 | 27500985 | + | Silent | SNP | C | C | T | TCGA-97-A4M3-01A-11D-A24P-08 | TCGA-97-A4M3-10A-01D-A24P-08 | g.chr16:27500985C>T | c.3231G>A | c.(3229-3231)gaG>gaA | p.E1077E |
| LUAD | 16 | 27504015 | 27504015 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-86-A4JF-01A-11D-A24P-08 | TCGA-86-A4JF-10A-01D-A24P-08 | g.chr16:27504015delC | c.2896delG | c.(2896-2898)gtgfs | p.V966fs |
| LUAD | 16 | 27504602 | 27504602 | + | Missense_Mutation | SNP | C | C | G | TCGA-97-A4LX-01A-11D-A24P-08 | TCGA-97-A4LX-10A-01D-A24P-08 | g.chr16:27504602C>G | c.2794G>C | c.(2794-2796)Gaa>Caa | p.E932Q |
| LUAD | 16 | 27506568 | 27506568 | + | Missense_Mutation | SNP | T | T | C | TCGA-78-7150-01A-21D-2036-08 | TCGA-78-7150-10A-01D-2036-08 | g.chr16:27506568T>C | c.2596A>G | c.(2596-2598)Acc>Gcc | p.T866A |
| LUAD | 16 | 27506573 | 27506573 | + | Missense_Mutation | SNP | C | C | A | TCGA-55-7570-01A-11D-2036-08 | TCGA-55-7570-10A-01D-2036-08 | g.chr16:27506573C>A | c.2591G>T | c.(2590-2592)gGt>gTt | p.G864V |
| LUAD | 16 | 27506630 | 27506630 | + | Missense_Mutation | SNP | G | G | A | TCGA-55-8208-01A-11D-2238-08 | TCGA-55-8208-10A-01D-2238-08 | g.chr16:27506630G>A | c.2534C>T | c.(2533-2535)tCc>tTc | p.S845F |
| LUAD | 16 | 27509014 | 27509014 | + | Missense_Mutation | SNP | T | T | A | TCGA-44-5644-01A-21D-2036-08 | TCGA-44-5644-10A-01D-2036-08 | g.chr16:27509014T>A | c.2294A>T | c.(2293-2295)aAa>aTa | p.K765I |
| LUAD | 16 | 27509024 | 27509024 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-78-7220-01A-11D-2036-08 | TCGA-78-7220-10A-01D-2036-08 | g.chr16:27509024C>A | c.2284G>T | c.(2284-2286)Gga>Tga | p.G762* |
| LUAD | 16 | 27512582 | 27512582 | + | Missense_Mutation | SNP | C | C | A | TCGA-64-5781-01A-01D-1625-08 | TCGA-64-5781-10A-01D-1625-08 | g.chr16:27512582C>A | c.1991G>T | c.(1990-1992)cGg>cTg | p.R664L |
| LUAD | 16 | 27517400 | 27517401 | + | Frame_Shift_Ins | INS | - | - | T | TCGA-05-4410-01A-21D-1855-08 | TCGA-05-4410-10A-01D-1855-08 | g.chr16:27517400_27517401insT | c.1589_1590insA | c.(1588-1590)aagfs | p.K530fs |
| LUAD | 16 | 27518169 | 27518169 | + | Splice_Site | SNP | C | C | A | TCGA-44-7671-01A-11D-2063-08 | TCGA-44-7671-10A-01D-2063-08 | g.chr16:27518169C>A | c.1551G>T | c.(1549-1551)aaG>aaT | p.K517N |
| LUAD | 16 | 27518331 | 27518331 | + | Missense_Mutation | SNP | C | C | A | TCGA-93-8067-01A-11D-2284-08 | TCGA-93-8067-10A-01D-2284-08 | g.chr16:27518331C>A | c.1389G>T | c.(1387-1389)gaG>gaT | p.E463D |
| LUAD | 16 | 27518346 | 27518346 | + | Silent | SNP | C | C | A | TCGA-55-8299-01A-11D-2284-08 | TCGA-55-8299-10B-01D-2323-08 | g.chr16:27518346C>A | c.1374G>T | c.(1372-1374)ctG>ctT | p.L458L |
| LUAD | 16 | 27518426 | 27518426 | + | Missense_Mutation | SNP | C | C | A | TCGA-86-8056-01A-11D-2238-08 | TCGA-86-8056-10A-01D-2238-08 | g.chr16:27518426C>A | c.1294G>T | c.(1294-1296)Gtg>Ttg | p.V432L |
| LUAD | 16 | 27519926 | 27519926 | + | Missense_Mutation | SNP | T | T | C | TCGA-17-Z055-01A-01W-0747-08 | TCGA-17-Z055-11A-01W-0747-08 | g.chr16:27519926T>C | c.1177A>G | c.(1177-1179)Atg>Gtg | p.M393V |
| LUAD | 16 | 27523148 | 27523148 | + | Missense_Mutation | SNP | C | C | G | TCGA-05-4390-01A-02D-1753-08 | TCGA-05-4390-10A-01D-1753-08 | g.chr16:27523148C>G | c.1048G>C | c.(1048-1050)Gag>Cag | p.E350Q |
| LUAD | 16 | 27540011 | 27540011 | + | Missense_Mutation | SNP | T | T | A | TCGA-44-2656-01A-02D-0969-08 | TCGA-44-2656-10A-01D-0969-08 | g.chr16:27540011T>A | c.881A>T | c.(880-882)tAc>tTc | p.Y294F |
| LUAD | 16 | 27544611 | 27544611 | + | Splice_Site | SNP | C | C | A | TCGA-69-7974-01A-11D-2184-08 | TCGA-69-7974-10A-01D-2184-08 | g.chr16:27544611C>A | | c.e5+1 | |
| LUAD | 16 | 27544624 | 27544624 | + | Silent | SNP | C | C | T | TCGA-38-4631-01A-01D-1753-08 | TCGA-38-4631-11A-01D-1753-08 | g.chr16:27544624C>T | c.837G>A | c.(835-837)ctG>ctA | p.L279L |
| LUAD | 16 | 27549128 | 27549128 | + | Silent | SNP | T | T | C | TCGA-53-7624-01A-11D-2063-08 | TCGA-53-7624-10A-01D-2063-08 | g.chr16:27549128T>C | c.729A>G | c.(727-729)ctA>ctG | p.L243L |
| LUAD | 16 | 27549551 | 27549551 | + | Silent | SNP | C | C | A | TCGA-78-7220-01A-11D-2036-08 | TCGA-78-7220-10A-01D-2036-08 | g.chr16:27549551C>A | c.558G>T | c.(556-558)cgG>cgT | p.R186R |
| LUAD | 16 | 27556834 | 27556834 | + | Missense_Mutation | SNP | T | T | A | TCGA-97-7547-01A-11D-2036-08 | TCGA-97-7547-10A-01D-2036-08 | g.chr16:27556834T>A | c.232A>T | c.(232-234)Att>Ttt | p.I78F |
| LUSC | 16 | 27480717 | 27480717 | + | Missense_Mutation | SNP | C | C | T | TCGA-37-5819-01A-01D-1632-08 | TCGA-37-5819-10A-01D-1632-08 | g.chr16:27480717C>T | c.4969G>A | c.(4969-4971)Gtc>Atc | p.V1657I |
| LUSC | 16 | 27495561 | 27495561 | + | Silent | SNP | G | G | A | TCGA-18-3415-01A-01D-0983-08 | TCGA-18-3415-11A-01D-0983-08 | g.chr16:27495561G>A | c.3972C>T | c.(3970-3972)gtC>gtT | p.V1324V |
| LUSC | 16 | 27497327 | 27497327 | + | Silent | SNP | G | G | T | TCGA-18-3419-01A-01D-0983-08 | TCGA-18-3419-11A-01D-0983-08 | g.chr16:27497327G>T | c.3849C>A | c.(3847-3849)ctC>ctA | p.L1283L |
| LUSC | 16 | 27497348 | 27497348 | + | Silent | SNP | G | G | A | TCGA-34-2596-01A-01D-1522-08 | TCGA-34-2596-11A-01D-1522-08 | g.chr16:27497348G>A | c.3828C>T | c.(3826-3828)tgC>tgT | p.C1276C |
| LUSC | 16 | 27503961 | 27503961 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-37-5819-01A-01D-1632-08 | TCGA-37-5819-10A-01D-1632-08 | g.chr16:27503961C>A | c.2950G>T | c.(2950-2952)Gaa>Taa | p.E984* |
| LUSC | 16 | 27504600 | 27504600 | + | Missense_Mutation | SNP | T | T | A | TCGA-43-3394-01A-01D-0983-08 | TCGA-43-3394-10A-01D-0983-08 | g.chr16:27504600T>A | c.2796A>T | c.(2794-2796)gaA>gaT | p.E932D |
| LUSC | 16 | 27506152 | 27506152 | + | Missense_Mutation | SNP | G | G | A | TCGA-18-3409-01A-01D-0983-08 | TCGA-18-3409-11A-01D-0983-08 | g.chr16:27506152G>A | c.2710C>T | c.(2710-2712)Ctc>Ttc | p.L904F |
| LUSC | 16 | 27509984 | 27509984 | + | Missense_Mutation | SNP | C | C | A | TCGA-66-2756-01A-01D-1522-08 | TCGA-66-2756-11A-01D-1522-08 | g.chr16:27509984C>A | c.2132G>T | c.(2131-2133)cGc>cTc | p.R711L |
| LUSC | 16 | 27518417 | 27518417 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-66-2727-01A-01D-0983-08 | TCGA-66-2727-11A-01D-0983-08 | g.chr16:27518417C>A | c.1303G>T | c.(1303-1305)Gag>Tag | p.E435* |
| OV | 16 | 27487836 | 27487851 | + | Frame_Shift_Del | DEL | TGAAGCACCAGAAAGT | TGAAGCACCAGAAAGT | - | TCGA-61-1914-01A-01W-0639-09 | TCGA-61-1914-11A-01W-0640-09 | g.chr16:27487836_27487851delTGAAGCACCAGAAAGT | c.4274_4289delACTTTCTGGTGCTTCA | c.(4273-4290)cactttctggtgcttcagfs | p.HFLVLQ1425fs |
| OV | 16 | 27501066 | 27501066 | + | Splice_Site | SNP | T | T | A | TCGA-23-2079-01A-01W-0722-08 | TCGA-23-2079-10A-01W-0722-08 | g.chr16:27501066T>A | | c.e20-2 | |
| OV | 16 | 27509110 | 27509110 | + | Missense_Mutation | SNP | C | C | T | TCGA-13-0903-01A-01W-0421-09 | TCGA-13-0903-10A-01W-0421-09 | g.chr16:27509110C>T | c.2198G>A | c.(2197-2199)gGg>gAg | p.G733E |
| OV | 16 | 27549656 | 27549656 | + | Silent | SNP | G | G | A | TCGA-23-2649-01A-01D-1526-09 | TCGA-23-2649-10A-01D-1526-09 | g.chr16:27549656G>A | c.453C>T | c.(451-453)atC>atT | p.I151I |
| OV | 16 | 27549676 | 27549676 | + | Splice_Site | SNP | A | A | C | TCGA-13-1512-01A-01W-0545-08 | TCGA-13-1512-10A-01W-0546-08 | g.chr16:27549676A>C | c.433T>G | c.(433-435)Tgg>Ggg | p.W145G |
| PAAD | 16 | 27473805 | 27473805 | + | Missense_Mutation | SNP | T | T | C | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr16:27473805T>C | c.5927A>G | c.(5926-5928)gAc>gGc | p.D1976G |
| PAAD | 16 | 27476061 | 27476061 | + | Missense_Mutation | SNP | G | G | A | TCGA-IB-AAUP-01A-11D-A377-08 | TCGA-IB-AAUP-10A-01D-A37A-08 | g.chr16:27476061G>A | c.5452C>T | c.(5452-5454)Cgg>Tgg | p.R1818W |
| PAAD | 16 | 27481690 | 27481690 | + | Missense_Mutation | SNP | G | G | T | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr16:27481690G>T | c.4553C>A | c.(4552-4554)aCc>aAc | p.T1518N |
| PAAD | 16 | 27481702 | 27481702 | + | Missense_Mutation | SNP | C | C | A | TCGA-HZ-A8P0-01A-11D-A36O-08 | TCGA-HZ-A8P0-10A-01D-A367-08 | g.chr16:27481702C>A | c.4541G>T | c.(4540-4542)cGa>cTa | p.R1514L |
| PAAD | 16 | 27495625 | 27495625 | + | Missense_Mutation | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr16:27495625G>A | c.3908C>T | c.(3907-3909)gCc>gTc | p.A1303V |
| PAAD | 16 | 27500951 | 27500951 | + | Missense_Mutation | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr16:27500951G>A | c.3265C>T | c.(3265-3267)Cgc>Tgc | p.R1089C |
| PAAD | 16 | 27503771 | 27503771 | + | Silent | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr16:27503771G>A | c.3039C>T | c.(3037-3039)aaC>aaT | p.N1013N |
| PAAD | 16 | 27506672 | 27506672 | + | Missense_Mutation | SNP | G | G | A | TCGA-IB-7651-01A-11D-2154-08 | TCGA-IB-7651-10A-01D-2154-08 | g.chr16:27506672G>A | c.2492C>T | c.(2491-2493)aCg>aTg | p.T831M |
| PAAD | 16 | 27517278 | 27517278 | + | Missense_Mutation | SNP | G | G | A | TCGA-2J-AABU-01A-11D-A40W-08 | TCGA-2J-AABU-10A-01D-A40W-08 | g.chr16:27517278G>A | c.1712C>T | c.(1711-1713)gCg>gTg | p.A571V |
| PCPG | 16 | 27523078 | 27523078 | + | Missense_Mutation | SNP | T | T | C | TCGA-W2-A7HC-01A-11D-A35I-08 | TCGA-W2-A7HC-10C-01D-A35G-08 | g.chr16:27523078T>C | c.1118A>G | c.(1117-1119)tAc>tGc | p.Y373C |
| PRAD | 16 | 27472773 | 27472773 | + | Silent | SNP | G | G | A | TCGA-J4-AATV-01A-11D-A41K-08 | TCGA-J4-AATV-10A-01D-A41N-08 | g.chr16:27472773G>A | c.6228C>T | c.(6226-6228)gaC>gaT | p.D2076D |
| PRAD | 16 | 27475706 | 27475706 | + | Missense_Mutation | SNP | C | C | A | TCGA-HC-7737-01A-11D-2114-08 | TCGA-HC-7737-11A-02D-2114-08 | g.chr16:27475706C>A | c.5807G>T | c.(5806-5808)aGt>aTt | p.S1936I |
| PRAD | 16 | 27481507 | 27481507 | + | Missense_Mutation | SNP | A | A | G | TCGA-J4-A67L-01A-11D-A30E-08 | TCGA-J4-A67L-10A-01D-A30H-08 | g.chr16:27481507A>G | c.4736T>C | c.(4735-4737)cTc>cCc | p.L1579P |
| PRAD | 16 | 27503740 | 27503740 | + | Missense_Mutation | SNP | G | G | A | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr16:27503740G>A | c.3070C>T | c.(3070-3072)Cgc>Tgc | p.R1024C |
| PRAD | 16 | 27506671 | 27506671 | + | Silent | SNP | C | C | T | TCGA-EJ-7315-01A-31D-2114-08 | TCGA-EJ-7315-10A-01D-2114-08 | g.chr16:27506671C>T | c.2493G>A | c.(2491-2493)acG>acA | p.T831T |
| PRAD | 16 | 27539921 | 27539921 | + | Missense_Mutation | SNP | T | T | C | TCGA-XK-AAIW-01A-11D-A41K-08 | TCGA-XK-AAIW-10A-01D-A41N-08 | g.chr16:27539921T>C | c.971A>G | c.(970-972)aAa>aGa | p.K324R |
| READ | 16 | 27476025 | 27476025 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr16:27476025C>A | c.5488G>T | c.(5488-5490)Gaa>Taa | p.E1830* |
| READ | 16 | 27499589 | 27499589 | + | Missense_Mutation | SNP | A | A | G | TCGA-F5-6702-01A-11D-1826-10 | TCGA-F5-6702-10A-01D-1826-10 | g.chr16:27499589A>G | c.3659T>C | c.(3658-3660)cTg>cCg | p.L1220P |
| READ | 16 | 27509109 | 27509109 | + | Silent | SNP | C | C | T | TCGA-F5-6813-01A-11D-1826-10 | TCGA-F5-6813-10A-01D-1826-10 | g.chr16:27509109C>T | c.2199G>A | c.(2197-2199)ggG>ggA | p.G733G |
| READ | 16 | 27512525 | 27512525 | + | Missense_Mutation | SNP | C | C | T | TCGA-AF-2693-01A-02D-1733-10 | TCGA-AF-2693-10A-01D-1733-10 | g.chr16:27512525C>T | c.2048G>A | c.(2047-2049)gGc>gAc | p.G683D |
| READ | 16 | 27549526 | 27549526 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-AG-A020-01A-21W-A096-10 | TCGA-AG-A020-11A-11W-A096-10 | g.chr16:27549526G>A | c.583C>T | c.(583-585)Cga>Tga | p.R195* |
| SARC | 16 | 27503659 | 27503659 | + | Splice_Site | SNP | C | C | T | TCGA-QC-A7B5-01A-11D-A33E-09 | TCGA-QC-A7B5-11A-11D-A33H-09 | g.chr16:27503659C>T | c.3151G>A | c.(3151-3153)Ggc>Agc | p.G1051S |
| SARC | 16 | 27509985 | 27509985 | + | Missense_Mutation | SNP | G | G | A | TCGA-DX-A3LY-01B-11D-A27P-09 | TCGA-DX-A3LY-10B-01D-A27P-09 | g.chr16:27509985G>A | c.2131C>T | c.(2131-2133)Cgc>Tgc | p.R711C |
| SARC | 16 | 27512569 | 27512569 | + | Silent | SNP | C | C | T | TCGA-DX-AB37-01A-11D-A417-09 | TCGA-DX-AB37-10A-01D-A41A-09 | g.chr16:27512569C>T | c.2004G>A | c.(2002-2004)gaG>gaA | p.E668E |
| SKCM | 16 | 27473718 | 27473718 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MS-06A-11D-A197-08 | TCGA-EE-A2MS-10A-01D-A199-08 | g.chr16:27473718G>A | c.6014C>T | c.(6013-6015)gCc>gTc | p.A2005V |
| SKCM | 16 | 27475728 | 27475728 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-EE-A2GO-06A-11D-A196-08 | TCGA-EE-A2GO-10A-01D-A198-08 | g.chr16:27475728G>A | c.5785C>T | c.(5785-5787)Caa>Taa | p.Q1929* |
| SKCM | 16 | 27475768 | 27475768 | + | Silent | SNP | A | A | G | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr16:27475768A>G | c.5745T>C | c.(5743-5745)gcT>gcC | p.A1915A |
| SKCM | 16 | 27475769 | 27475769 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr16:27475769G>A | c.5744C>T | c.(5743-5745)gCt>gTt | p.A1915V |
| SKCM | 16 | 27475784 | 27475784 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2GR-06A-11D-A197-08 | TCGA-EE-A2GR-10A-01D-A199-08 | g.chr16:27475784G>A | c.5729C>T | c.(5728-5730)cCa>cTa | p.P1910L |
| SKCM | 16 | 27475829 | 27475829 | + | Missense_Mutation | SNP | G | G | A | TCGA-FS-A1ZK-06A-11D-A197-08 | TCGA-FS-A1ZK-10A-01D-A199-08 | g.chr16:27475829G>A | c.5684C>T | c.(5683-5685)cCc>cTc | p.P1895L |
| SKCM | 16 | 27475830 | 27475830 | + | Missense_Mutation | SNP | G | G | A | TCGA-FS-A1ZK-06A-11D-A197-08 | TCGA-FS-A1ZK-10A-01D-A199-08 | g.chr16:27475830G>A | c.5683C>T | c.(5683-5685)Ccc>Tcc | p.P1895S |
| SKCM | 16 | 27476005 | 27476005 | + | Silent | SNP | G | G | A | TCGA-FS-A1ZK-06A-11D-A197-08 | TCGA-FS-A1ZK-10A-01D-A199-08 | g.chr16:27476005G>A | c.5508C>T | c.(5506-5508)ccC>ccT | p.P1836P |
| SKCM | 16 | 27476006 | 27476006 | + | Missense_Mutation | SNP | G | G | A | TCGA-FS-A1ZK-06A-11D-A197-08 | TCGA-FS-A1ZK-10A-01D-A199-08 | g.chr16:27476006G>A | c.5507C>T | c.(5506-5508)cCc>cTc | p.P1836L |
| SKCM | 16 | 27476016 | 27476016 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-EE-A3JE-06A-11D-A20D-08 | TCGA-EE-A3JE-10A-01D-A20D-08 | g.chr16:27476016G>A | c.5497C>T | c.(5497-5499)Cag>Tag | p.Q1833* |
| SKCM | 16 | 27476020 | 27476020 | + | Silent | SNP | G | G | A | TCGA-EE-A2GI-06A-11D-A196-08 | TCGA-EE-A2GI-10A-01D-A198-08 | g.chr16:27476020G>A | c.5493C>T | c.(5491-5493)gaC>gaT | p.D1831D |
| SKCM | 16 | 27480632 | 27480632 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29E-06A-11D-A197-08 | TCGA-EE-A29E-10A-01D-A199-08 | g.chr16:27480632G>A | c.5054C>T | c.(5053-5055)cCc>cTc | p.P1685L |
| SKCM | 16 | 27481489 | 27481489 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29S-06A-11D-A197-08 | TCGA-EE-A29S-10A-01D-A199-08 | g.chr16:27481489C>T | c.4754G>A | c.(4753-4755)aGg>aAg | p.R1585K |
| SKCM | 16 | 27481569 | 27481569 | + | Silent | SNP | G | G | A | TCGA-FS-A1ZK-06A-11D-A197-08 | TCGA-FS-A1ZK-10A-01D-A199-08 | g.chr16:27481569G>A | c.4674C>T | c.(4672-4674)gcC>gcT | p.A1558A |
| SKCM | 16 | 27481622 | 27481622 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2GB-06A-11D-A197-08 | TCGA-EE-A2GB-10A-01D-A199-08 | g.chr16:27481622G>A | c.4621C>T | c.(4621-4623)Cgt>Tgt | p.R1541C |
| SKCM | 16 | 27483215 | 27483215 | + | Silent | SNP | C | C | T | TCGA-EE-A29M-06A-11D-A196-08 | TCGA-EE-A29M-10A-01D-A198-08 | g.chr16:27483215C>T | c.4380G>A | c.(4378-4380)aaG>aaA | p.K1460K |
| SKCM | 16 | 27487825 | 27487825 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-EE-A3AE-06A-11D-A196-08 | TCGA-EE-A3AE-10A-01D-A198-08 | g.chr16:27487825G>A | c.4300C>T | c.(4300-4302)Cag>Tag | p.Q1434* |
| SKCM | 16 | 27495589 | 27495589 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A3MR-06A-11D-A21A-08 | TCGA-D3-A3MR-10A-01D-A21A-08 | g.chr16:27495589G>A | c.3944C>T | c.(3943-3945)tCc>tTc | p.S1315F |
| SKCM | 16 | 27495610 | 27495610 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A2J7-06A-11D-A196-08 | TCGA-D3-A2J7-10A-01D-A198-08 | g.chr16:27495610G>A | c.3923C>T | c.(3922-3924)tCt>tTt | p.S1308F |
| SKCM | 16 | 27495610 | 27495610 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2GC-06A-11D-A197-08 | TCGA-EE-A2GC-10A-01D-A199-08 | g.chr16:27495610G>A | c.3923C>T | c.(3922-3924)tCt>tTt | p.S1308F |
| SKCM | 16 | 27497395 | 27497395 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2MR-06A-11D-A196-08 | TCGA-EE-A2MR-10A-01D-A198-08 | g.chr16:27497395G>A | c.3781C>T | c.(3781-3783)Ctt>Ttt | p.L1261F |
| SKCM | 16 | 27497466 | 27497466 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A2GR-06A-11D-A197-08 | TCGA-EE-A2GR-10A-01D-A199-08 | g.chr16:27497466G>A | c.3710C>T | c.(3709-3711)cCa>cTa | p.P1237L |
| SKCM | 16 | 27499546 | 27499546 | + | Splice_Site | SNP | A | A | G | TCGA-EE-A3AC-06A-11D-A196-08 | TCGA-EE-A3AC-10A-01D-A198-08 | g.chr16:27499546A>G | | c.e23+1 | |
| SKCM | 16 | 27499675 | 27499675 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-D3-A2JD-06A-11D-A19A-08 | TCGA-D3-A2JD-10A-01D-A19A-08 | g.chr16:27499675C>T | c.3573G>A | c.(3571-3573)tgG>tgA | p.W1191* |
| SKCM | 16 | 27503759 | 27503759 | + | Silent | SNP | G | G | A | TCGA-EE-A2M5-06A-12D-A197-08 | TCGA-EE-A2M5-10A-01D-A199-08 | g.chr16:27503759G>A | c.3051C>T | c.(3049-3051)agC>agT | p.S1017S |
| SKCM | 16 | 27503770 | 27503770 | + | Silent | SNP | G | G | A | TCGA-FS-A1ZQ-06A-11D-A197-08 | TCGA-FS-A1ZQ-10A-01D-A199-08 | g.chr16:27503770G>A | c.3040C>T | c.(3040-3042)Ctg>Ttg | p.L1014L |
| SKCM | 16 | 27504020 | 27504020 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A181-06A-11D-A196-08 | TCGA-EE-A181-10A-01D-A198-08 | g.chr16:27504020G>A | c.2891C>T | c.(2890-2892)tCg>tTg | p.S964L |
| SKCM | 16 | 27504563 | 27504563 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A20C-06A-11D-A196-08 | TCGA-EE-A20C-10A-01D-A198-08 | g.chr16:27504563G>A | c.2833C>T | c.(2833-2835)Cgc>Tgc | p.R945C |
| SKCM | 16 | 27506150 | 27506150 | + | Silent | SNP | G | G | A | TCGA-EE-A3J7-06A-11D-A20D-08 | TCGA-EE-A3J7-10A-01D-A20D-08 | g.chr16:27506150G>A | c.2712C>T | c.(2710-2712)ctC>ctT | p.L904L |
| SKCM | 16 | 27506184 | 27506184 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29E-06A-11D-A197-08 | TCGA-EE-A29E-10A-01D-A199-08 | g.chr16:27506184G>A | c.2678C>T | c.(2677-2679)cCa>cTa | p.P893L |
| SKCM | 16 | 27506194 | 27506194 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr16:27506194G>A | c.2668C>T | c.(2668-2670)Ccc>Tcc | p.P890S |
| SKCM | 16 | 27506539 | 27506539 | + | Silent | SNP | C | C | T | TCGA-EE-A20C-06A-11D-A196-08 | TCGA-EE-A20C-10A-01D-A198-08 | g.chr16:27506539C>T | c.2625G>A | c.(2623-2625)acG>acA | p.T875T |
| SKCM | 16 | 27506677 | 27506677 | + | Silent | SNP | C | C | T | TCGA-GF-A3OT-06A-23D-A23B-08 | TCGA-GF-A3OT-10A-01D-A23B-08 | g.chr16:27506677C>T | c.2487G>A | c.(2485-2487)cgG>cgA | p.R829R |
| SKCM | 16 | 27506734 | 27506734 | + | Silent | SNP | G | G | A | TCGA-EE-A29Q-06A-11D-A197-08 | TCGA-EE-A29Q-10A-01D-A199-08 | g.chr16:27506734G>A | c.2430C>T | c.(2428-2430)ctC>ctT | p.L810L |
| SKCM | 16 | 27517295 | 27517295 | + | Silent | SNP | G | G | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr16:27517295G>T | c.1695C>A | c.(1693-1695)tcC>tcA | p.S565S |
| SKCM | 16 | 27517296 | 27517296 | + | Missense_Mutation | SNP | G | G | A | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr16:27517296G>A | c.1694C>T | c.(1693-1695)tCc>tTc | p.S565F |
| SKCM | 16 | 27519910 | 27519910 | + | Missense_Mutation | SNP | A | A | T | TCGA-ER-A19F-06A-11D-A196-08 | TCGA-ER-A19F-10A-01D-A198-08 | g.chr16:27519910A>T | c.1193T>A | c.(1192-1194)cTa>cAa | p.L398Q |
| SKCM | 16 | 27519956 | 27519956 | + | Missense_Mutation | SNP | C | C | T | TCGA-D3-A1Q5-06A-11D-A196-08 | TCGA-D3-A1Q5-10A-01D-A198-08 | g.chr16:27519956C>T | c.1147G>A | c.(1147-1149)Gga>Aga | p.G383R |
| SKCM | 16 | 27523104 | 27523104 | + | Silent | SNP | G | G | A | TCGA-EE-A181-06A-11D-A196-08 | TCGA-EE-A181-10A-01D-A198-08 | g.chr16:27523104G>A | c.1092C>T | c.(1090-1092)ttC>ttT | p.F364F |
| SKCM | 16 | 27549248 | 27549248 | + | Splice_Site | SNP | C | C | T | TCGA-EE-A3AG-06A-31D-A196-08 | TCGA-EE-A3AG-10A-01D-A198-08 | g.chr16:27549248C>T | c.609G>A | c.(607-609)aaG>aaA | p.K203K |
| SKCM | 16 | 27549503 | 27549503 | + | Silent | SNP | G | G | A | TCGA-EE-A3AA-06A-11D-A196-08 | TCGA-EE-A3AA-10A-01D-A198-08 | g.chr16:27549503G>A | c.606C>T | c.(604-606)ttC>ttT | p.F202F |
| SKCM | 16 | 27556757 | 27556757 | + | Silent | SNP | G | G | A | TCGA-EE-A2MJ-06A-11D-A197-08 | TCGA-EE-A2MJ-10A-01D-A199-08 | g.chr16:27556757G>A | c.309C>T | c.(307-309)atC>atT | p.I103I |
| SKCM | 16 | 27556771 | 27556771 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A3MR-06A-11D-A21A-08 | TCGA-D3-A3MR-10A-01D-A21A-08 | g.chr16:27556771G>A | c.295C>T | c.(295-297)Ccc>Tcc | p.P99S |
| SKCM | 16 | 27556813 | 27556813 | + | Missense_Mutation | SNP | A | A | C | TCGA-D3-A2JN-06A-11D-A196-08 | TCGA-D3-A2JN-10A-01D-A198-08 | g.chr16:27556813A>C | c.253T>G | c.(253-255)Ttg>Gtg | p.L85V |
| SKCM | 16 | 27561109 | 27561109 | + | Missense_Mutation | SNP | A | A | G | TCGA-EE-A2MJ-06A-11D-A197-08 | TCGA-EE-A2MJ-10A-01D-A199-08 | g.chr16:27561109A>G | c.103T>C | c.(103-105)Ttc>Ctc | p.F35L |
| SKCM | 16 | 27561133 | 27561133 | + | Missense_Mutation | SNP | G | G | A | TCGA-D3-A5GL-06A-11D-A27K-08 | TCGA-D3-A5GL-10A-01D-A27N-08 | g.chr16:27561133G>A | c.79C>T | c.(79-81)Cgg>Tgg | p.R27W |