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 | 4 | 16504433 | 16504433 | + | Silent | SNP | G | G | A | TCGA-ZF-A9RD-01A-11D-A42E-08 | TCGA-ZF-A9RD-10A-01D-A42H-08 | g.chr4:16504433G>A | c.955C>T | c.(955-957)Cta>Tta | p.L319L |
BLCA | 4 | 16510157 | 16510157 | + | Splice_Site | SNP | C | C | G | TCGA-E7-A541-01A-11D-A26M-08 | TCGA-E7-A541-10A-01D-A26K-08 | g.chr4:16510157C>G | | c.e7+1 | |
BLCA | 4 | 16587581 | 16587581 | + | Missense_Mutation | SNP | C | C | A | TCGA-ZF-AA4X-01A-11D-A38G-08 | TCGA-ZF-AA4X-10A-01D-A38J-08 | g.chr4:16587581C>A | c.579G>T | c.(577-579)agG>agT | p.R193S |
BLCA | 4 | 16590352 | 16590352 | + | Missense_Mutation | SNP | C | C | G | TCGA-FD-A3SS-01A-12D-A22Z-08 | TCGA-FD-A3SS-10A-01D-A22Z-08 | g.chr4:16590352C>G | c.512G>C | c.(511-513)aGa>aCa | p.R171T |
BLCA | 4 | 16590367 | 16590367 | + | Missense_Mutation | SNP | C | C | T | TCGA-4Z-AA7O-01A-31D-A391-08 | TCGA-4Z-AA7O-10A-01D-A394-08 | g.chr4:16590367C>T | c.497G>A | c.(496-498)cGa>cAa | p.R166Q |
BLCA | 4 | 16597444 | 16597444 | + | Missense_Mutation | SNP | A | A | C | TCGA-G2-A2ES-01A-11D-A17V-08 | TCGA-G2-A2ES-11A-31D-A17V-08 | g.chr4:16597444A>C | c.290T>G | c.(289-291)gTg>gGg | p.V97G |
BLCA | 4 | 16760787 | 16760787 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-XF-A9ST-01A-11D-A42E-08 | TCGA-XF-A9ST-10A-01D-A42H-08 | g.chr4:16760787G>A | c.229C>T | c.(229-231)Cga>Tga | p.R77* |
BLCA | 4 | 16900009 | 16900009 | + | Missense_Mutation | SNP | C | C | T | TCGA-C4-A0F6-01A-11D-A10S-08 | TCGA-C4-A0F6-10A-01D-A10S-08 | g.chr4:16900009C>T | c.100G>A | c.(100-102)Gag>Aag | p.E34K |
BLCA | 4 | 16900017 | 16900017 | + | Missense_Mutation | SNP | C | C | T | TCGA-GV-A3QI-01A-11D-A21Z-08 | TCGA-GV-A3QI-10A-01D-A21Z-08 | g.chr4:16900017C>T | c.92G>A | c.(91-93)cGa>cAa | p.R31Q |
BLCA | 4 | 16900019 | 16900019 | + | Silent | SNP | G | G | A | TCGA-5N-A9KM-01A-11D-A42E-08 | TCGA-5N-A9KM-10A-01D-A42H-08 | g.chr4:16900019G>A | c.90C>T | c.(88-90)taC>taT | p.Y30Y |
BRCA | 4 | 16504298 | 16504298 | + | Missense_Mutation | SNP | A | A | T | TCGA-A2-A0CU-01A-12W-A050-09 | TCGA-A2-A0CU-10A-01W-A055-09 | g.chr4:16504298A>T | c.1090T>A | c.(1090-1092)Tca>Aca | p.S364T |
BRCA | 4 | 16504398 | 16504398 | + | Silent | SNP | C | C | T | TCGA-BH-A0HB-01A-11W-A071-09 | TCGA-BH-A0HB-10A-01W-A071-09 | g.chr4:16504398C>T | c.990G>A | c.(988-990)gcG>gcA | p.A330A |
BRCA | 4 | 16504411 | 16504411 | + | Missense_Mutation | SNP | G | G | A | TCGA-BH-A1F8-01A-11D-A13L-09 | TCGA-BH-A1F8-11B-21D-A188-09 | g.chr4:16504411G>A | c.977C>T | c.(976-978)aCg>aTg | p.T326M |
BRCA | 4 | 16504486 | 16504486 | + | Missense_Mutation | SNP | A | A | C | TCGA-A2-A0T5-01A-21D-A099-09 | TCGA-A2-A0T5-10A-01D-A099-09 | g.chr4:16504486A>C | c.902T>G | c.(901-903)gTg>gGg | p.V301G |
BRCA | 4 | 16507531 | 16507532 | + | Intron | DNP | GG | GG | CT | TCGA-A8-A07C-01A-11D-A045-09 | TCGA-A8-A07C-10A-01W-A055-09 | g.chr4:16507531_16507532GG>CT | | | |
BRCA | 4 | 16587601 | 16587601 | + | Missense_Mutation | SNP | G | G | T | TCGA-A7-A0CE-01A-11W-A019-09 | TCGA-A7-A0CE-10A-01W-A021-09 | g.chr4:16587601G>T | c.559C>A | c.(559-561)Ctg>Atg | p.L187M |
BRCA | 4 | 16597371 | 16597371 | + | Missense_Mutation | SNP | G | G | T | TCGA-A2-A04Y-01A-21W-A050-09 | TCGA-A2-A04Y-10A-01W-A055-09 | g.chr4:16597371G>T | c.363C>A | c.(361-363)gaC>gaA | p.D121E |
BRCA | 4 | 16597474 | 16597474 | + | Missense_Mutation | SNP | C | C | T | TCGA-A8-A08J-01A-11W-A019-09 | TCGA-A8-A08J-10A-01W-A021-09 | g.chr4:16597474C>T | c.260G>A | c.(259-261)cGt>cAt | p.R87H |
BRCA | 4 | 16899985 | 16899985 | + | Missense_Mutation | SNP | G | G | A | TCGA-EW-A1IZ-01A-11D-A188-09 | TCGA-EW-A1IZ-10A-01D-A13O-09 | g.chr4:16899985G>A | c.124C>T | c.(124-126)Cgc>Tgc | p.R42C |
CESC | 4 | 16590405 | 16590405 | + | Missense_Mutation | SNP | C | C | G | TCGA-Q1-A73O-01A-11D-A32I-09 | TCGA-Q1-A73O-10B-01D-A32I-09 | g.chr4:16590405C>G | c.459G>C | c.(457-459)atG>atC | p.M153I |
CESC | 4 | 16590439 | 16590439 | + | Missense_Mutation | SNP | C | C | G | TCGA-EK-A2RA-01A-11D-A18J-09 | TCGA-EK-A2RA-10A-01D-A18J-09 | g.chr4:16590439C>G | c.425G>C | c.(424-426)aGa>aCa | p.R142T |
COAD | 4 | 16504316 | 16504316 | + | Missense_Mutation | SNP | C | C | T | TCGA-AD-6889-01A-11D-1924-10 | TCGA-AD-6889-10A-01D-1924-10 | g.chr4:16504316C>T | c.1072G>A | c.(1072-1074)Gcc>Acc | p.A358T |
COAD | 4 | 16504335 | 16504335 | + | Silent | SNP | C | C | T | TCGA-AA-3554-01A-01W-0833-10 | TCGA-AA-3554-10A-01W-0833-10 | g.chr4:16504335C>T | c.1053G>A | c.(1051-1053)ccG>ccA | p.P351P |
COAD | 4 | 16504355 | 16504355 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-6540-01A-11D-1719-10 | TCGA-D5-6540-10A-01D-1719-10 | g.chr4:16504355C>T | c.1033G>A | c.(1033-1035)Gcg>Acg | p.A345T |
COAD | 4 | 16510259 | 16510259 | + | Missense_Mutation | SNP | T | T | A | TCGA-D5-6535-01A-11D-1719-10 | TCGA-D5-6535-10A-01D-1719-10 | g.chr4:16510259T>A | c.790A>T | c.(790-792)Acc>Tcc | p.T264S |
COAD | 4 | 16513609 | 16513609 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3538-01A-01W-0831-10 | TCGA-AA-3538-10A-01W-0831-10 | g.chr4:16513609G>A | c.734C>T | c.(733-735)cCg>cTg | p.P245L |
COAD | 4 | 16597347 | 16597347 | + | Silent | SNP | G | G | A | TCGA-CM-6172-01A-11D-1650-10 | TCGA-CM-6172-10A-01D-1650-10 | g.chr4:16597347G>A | c.387C>T | c.(385-387)caC>caT | p.H129H |
COADREAD | 4 | 16504316 | 16504316 | + | Missense_Mutation | SNP | C | C | T | TCGA-AD-6889-01A-11D-1924-10 | TCGA-AD-6889-10A-01D-1924-10 | g.chr4:16504316C>T | c.1072G>A | c.(1072-1074)Gcc>Acc | p.A358T |
COADREAD | 4 | 16504335 | 16504335 | + | Silent | SNP | C | C | T | TCGA-AA-3554-01A-01W-0833-10 | TCGA-AA-3554-10A-01W-0833-10 | g.chr4:16504335C>T | c.1053G>A | c.(1051-1053)ccG>ccA | p.P351P |
COADREAD | 4 | 16504355 | 16504355 | + | Missense_Mutation | SNP | C | C | T | TCGA-D5-6540-01A-11D-1719-10 | TCGA-D5-6540-10A-01D-1719-10 | g.chr4:16504355C>T | c.1033G>A | c.(1033-1035)Gcg>Acg | p.A345T |
COADREAD | 4 | 16510259 | 16510259 | + | Missense_Mutation | SNP | T | T | A | TCGA-D5-6535-01A-11D-1719-10 | TCGA-D5-6535-10A-01D-1719-10 | g.chr4:16510259T>A | c.790A>T | c.(790-792)Acc>Tcc | p.T264S |
COADREAD | 4 | 16513609 | 16513609 | + | Missense_Mutation | SNP | G | G | A | TCGA-AA-3538-01A-01W-0831-10 | TCGA-AA-3538-10A-01W-0831-10 | g.chr4:16513609G>A | c.734C>T | c.(733-735)cCg>cTg | p.P245L |
COADREAD | 4 | 16597347 | 16597347 | + | Silent | SNP | G | G | A | TCGA-CM-6172-01A-11D-1650-10 | TCGA-CM-6172-10A-01D-1650-10 | g.chr4:16597347G>A | c.387C>T | c.(385-387)caC>caT | p.H129H |
COADREAD | 4 | 16597494 | 16597494 | + | Silent | SNP | G | G | A | TCGA-DC-6158-01A-11D-1657-10 | TCGA-DC-6158-10A-01D-1657-10 | g.chr4:16597494G>A | c.240C>T | c.(238-240)atC>atT | p.I80I |
COADREAD | 4 | 16760787 | 16760787 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr4:16760787G>A | c.229C>T | c.(229-231)Cga>Tga | p.R77* |
ESCA | 4 | 16900009 | 16900009 | + | Missense_Mutation | SNP | C | C | G | TCGA-Q9-A6FU-01A-11D-A31U-09 | TCGA-Q9-A6FU-10A-01D-A31U-09 | g.chr4:16900009C>G | c.100G>C | c.(100-102)Gag>Cag | p.E34Q |
ESCA | 4 | 16900100 | 16900100 | + | Missense_Mutation | SNP | G | G | T | TCGA-IG-A4QS-01A-11D-A27G-09 | TCGA-IG-A4QS-10A-01D-A27G-09 | g.chr4:16900100G>T | c.9C>A | c.(7-9)agC>agA | p.S3R |
GBMLGG | 4 | 16504355 | 16504355 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr4:16504355C>T | c.1033G>A | c.(1033-1035)Gcg>Acg | p.A345T |
HNSC | 4 | 16513685 | 16513685 | + | Missense_Mutation | SNP | G | G | A | TCGA-CV-7245-01A-11D-2012-08 | TCGA-CV-7245-10A-01D-2013-08 | g.chr4:16513685G>A | c.658C>T | c.(658-660)Cat>Tat | p.H220Y |
HNSC | 4 | 16590360 | 16590360 | + | Silent | SNP | T | T | C | TCGA-D6-A6EO-01A-11D-A31L-08 | TCGA-D6-A6EO-10A-01D-A31J-08 | g.chr4:16590360T>C | c.504A>G | c.(502-504)ttA>ttG | p.L168L |
HNSC | 4 | 16590367 | 16590367 | + | Missense_Mutation | SNP | C | C | A | TCGA-BA-5152-01A-02D-1870-08 | TCGA-BA-5152-10A-01D-1870-08 | g.chr4:16590367C>A | c.497G>T | c.(496-498)cGa>cTa | p.R166L |
HNSC | 4 | 16760797 | 16760797 | + | Silent | SNP | A | A | G | TCGA-CN-6010-01A-11D-1683-08 | TCGA-CN-6010-10A-01D-1683-08 | g.chr4:16760797A>G | c.219T>C | c.(217-219)gaT>gaC | p.D73D |
HNSC | 4 | 16760821 | 16760821 | + | Missense_Mutation | SNP | T | T | A | TCGA-CR-7371-01A-11D-2012-08 | TCGA-CR-7371-10A-01D-2013-08 | g.chr4:16760821T>A | c.195A>T | c.(193-195)ttA>ttT | p.L65F |
HNSC | 4 | 16760850 | 16760850 | + | Missense_Mutation | SNP | T | T | A | TCGA-CV-A461-01A-41D-A25Y-08 | TCGA-CV-A461-10A-01D-A25Y-08 | g.chr4:16760850T>A | c.166A>T | c.(166-168)Act>Tct | p.T56S |
LGG | 4 | 16504355 | 16504355 | + | Missense_Mutation | SNP | C | C | T | TCGA-DU-6392-01A-11D-1705-08 | TCGA-DU-6392-10A-01D-1705-08 | g.chr4:16504355C>T | c.1033G>A | c.(1033-1035)Gcg>Acg | p.A345T |
LIHC | 4 | 16510279 | 16510279 | + | Missense_Mutation | SNP | C | C | T | TCGA-CC-A5UD-01A-11D-A28X-10 | TCGA-CC-A5UD-10A-01D-A28X-10 | g.chr4:16510279C>T | c.770G>A | c.(769-771)cGg>cAg | p.R257Q |
LIHC | 4 | 16900005 | 16900005 | + | Missense_Mutation | SNP | A | A | G | TCGA-DD-AADR-01A-11D-A40R-10 | TCGA-DD-AADR-10A-01D-A40U-10 | g.chr4:16900005A>G | c.104T>C | c.(103-105)aTg>aCg | p.M35T |
LUAD | 4 | 16504268 | 16504268 | + | Nonstop_Mutation | SNP | A | A | C | TCGA-44-A47G-01A-21D-A24D-08 | TCGA-44-A47G-10A-01D-A24F-08 | g.chr4:16504268A>C | c.1120T>G | c.(1120-1122)Taa>Gaa | p.*374E |
LUAD | 4 | 16504337 | 16504337 | + | Missense_Mutation | SNP | G | G | T | TCGA-62-8399-01A-21D-2323-08 | TCGA-62-8399-10A-01D-2323-08 | g.chr4:16504337G>T | c.1051C>A | c.(1051-1053)Ccg>Acg | p.P351T |
LUAD | 4 | 16504338 | 16504338 | + | Missense_Mutation | SNP | G | G | T | TCGA-55-8506-01A-11D-2393-08 | TCGA-55-8506-10A-01D-2393-08 | g.chr4:16504338G>T | c.1050C>A | c.(1048-1050)agC>agA | p.S350R |
LUAD | 4 | 16504354 | 16504354 | + | Missense_Mutation | SNP | G | G | A | TCGA-55-8507-01A-11D-2393-08 | TCGA-55-8507-10A-01D-2393-08 | g.chr4:16504354G>A | c.1034C>T | c.(1033-1035)gCg>gTg | p.A345V |
LUAD | 4 | 16504379 | 16504379 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-62-A46P-01A-11D-A24D-08 | TCGA-62-A46P-10A-01D-A24F-08 | g.chr4:16504379C>A | c.1009G>T | c.(1009-1011)Gag>Tag | p.E337* |
LUAD | 4 | 16504392 | 16504392 | + | Missense_Mutation | SNP | G | G | T | TCGA-J2-A4AD-01A-11D-A24D-08 | TCGA-J2-A4AD-10A-01D-A24F-08 | g.chr4:16504392G>T | c.996C>A | c.(994-996)aaC>aaA | p.N332K |
LUAD | 4 | 16513681 | 16513681 | + | Missense_Mutation | SNP | T | T | A | TCGA-55-8507-01A-11D-2393-08 | TCGA-55-8507-10A-01D-2393-08 | g.chr4:16513681T>A | c.662A>T | c.(661-663)aAa>aTa | p.K221I |
LUAD | 4 | 16513703 | 16513703 | + | Missense_Mutation | SNP | G | G | C | TCGA-91-6829-01A-21D-1855-08 | TCGA-91-6829-11A-01D-1855-08 | g.chr4:16513703G>C | c.640C>G | c.(640-642)Cag>Gag | p.Q214E |
LUAD | 4 | 16513703 | 16513703 | + | Missense_Mutation | SNP | G | G | T | TCGA-50-6590-01A-12D-1855-08 | TCGA-50-6590-11A-01D-1855-08 | g.chr4:16513703G>T | c.640C>A | c.(640-642)Cag>Aag | p.Q214K |
LUAD | 4 | 16587547 | 16587547 | + | Missense_Mutation | SNP | T | T | A | TCGA-55-8506-01A-11D-2393-08 | TCGA-55-8506-10A-01D-2393-08 | g.chr4:16587547T>A | c.613A>T | c.(613-615)Agg>Tgg | p.R205W |
LUAD | 4 | 16587550 | 16587550 | + | Missense_Mutation | SNP | G | G | T | TCGA-64-1679-01A-21D-2063-08 | TCGA-64-1679-10A-01D-2063-08 | g.chr4:16587550G>T | c.610C>A | c.(610-612)Ctc>Atc | p.L204I |
LUAD | 4 | 16590406 | 16590406 | + | Missense_Mutation | SNP | A | A | T | TCGA-05-4382-01A-01D-1931-08 | TCGA-05-4382-10A-01D-1265-08 | g.chr4:16590406A>T | c.458T>A | c.(457-459)aTg>aAg | p.M153K |
LUAD | 4 | 16590420 | 16590420 | + | Silent | SNP | G | G | T | TCGA-50-5051-01A-21D-1855-08 | TCGA-50-5051-10A-01D-1855-08 | g.chr4:16590420G>T | c.444C>A | c.(442-444)acC>acA | p.T148T |
LUAD | 4 | 16597424 | 16597424 | + | Missense_Mutation | SNP | G | G | T | TCGA-50-5935-01A-11D-1753-08 | TCGA-50-5935-11A-01D-1753-08 | g.chr4:16597424G>T | c.310C>A | c.(310-312)Ctc>Atc | p.L104I |
LUAD | 4 | 16597466 | 16597466 | + | Missense_Mutation | SNP | T | T | C | TCGA-05-4390-01A-02D-1753-08 | TCGA-05-4390-10A-01D-1753-08 | g.chr4:16597466T>C | c.268A>G | c.(268-270)Agc>Ggc | p.S90G |
LUAD | 4 | 16597468 | 16597468 | + | Missense_Mutation | SNP | A | A | T | TCGA-97-A4M7-01A-11D-A24P-08 | TCGA-97-A4M7-10A-01D-A24P-08 | g.chr4:16597468A>T | c.266T>A | c.(265-267)tTt>tAt | p.F89Y |
LUAD | 4 | 16597475 | 16597475 | + | Missense_Mutation | SNP | G | G | C | TCGA-55-8085-01A-11D-2238-08 | TCGA-55-8085-10A-01D-2238-08 | g.chr4:16597475G>C | c.259C>G | c.(259-261)Cgt>Ggt | p.R87G |
LUAD | 4 | 16760782 | 16760782 | + | Splice_Site | SNP | G | G | C | TCGA-55-8299-01A-11D-2284-08 | TCGA-55-8299-10B-01D-2323-08 | g.chr4:16760782G>C | c.234C>G | c.(232-234)taC>taG | p.Y78* |
LUAD | 4 | 16760835 | 16760835 | + | Missense_Mutation | SNP | C | C | A | TCGA-17-Z014-01A-01W-0746-08 | TCGA-17-Z014-11A-01W-0746-08 | g.chr4:16760835C>A | c.181G>T | c.(181-183)Gat>Tat | p.D61Y |
LUAD | 4 | 16760880 | 16760880 | + | Missense_Mutation | SNP | T | T | G | TCGA-38-4628-01A-01D-1265-08 | TCGA-38-4628-11A-01D-1265-08 | g.chr4:16760880T>G | c.136A>C | c.(136-138)Agt>Cgt | p.S46R |
LUAD | 4 | 16899977 | 16899977 | + | Splice_Site | SNP | C | C | T | TCGA-05-4427-01A-21D-1855-08 | TCGA-05-4427-10A-01D-1855-08 | g.chr4:16899977C>T | c.132G>A | c.(130-132)gaG>gaA | p.E44E |
LUAD | 4 | 16900033 | 16900033 | + | Frame_Shift_Del | DEL | C | C | - | TCGA-44-8120-01A-11D-2238-08 | TCGA-44-8120-10A-01D-2238-08 | g.chr4:16900033delC | c.76delG | c.(76-78)gtafs | p.V26fs |
LUAD | 4 | 16900063 | 16900063 | + | Missense_Mutation | SNP | G | G | C | TCGA-05-4417-01A-22D-1855-08 | TCGA-05-4417-10A-01D-1855-08 | g.chr4:16900063G>C | c.46C>G | c.(46-48)Cca>Gca | p.P16A |
LUAD | 4 | 16900066 | 16900066 | + | Missense_Mutation | SNP | C | C | T | TCGA-95-8039-01A-11D-2238-08 | TCGA-95-8039-10A-01D-2238-08 | g.chr4:16900066C>T | c.43G>A | c.(43-45)Ggc>Agc | p.G15S |
LUSC | 4 | 16504392 | 16504392 | + | Missense_Mutation | SNP | G | G | T | TCGA-43-2578-01A-01D-1522-08 | TCGA-43-2578-11A-01D-1522-08 | g.chr4:16504392G>T | c.996C>A | c.(994-996)aaC>aaA | p.N332K |
LUSC | 4 | 16504481 | 16504481 | + | Nonsense_Mutation | SNP | C | C | A | TCGA-66-2787-01A-01D-0983-08 | TCGA-66-2787-11A-01D-0983-08 | g.chr4:16504481C>A | c.907G>T | c.(907-909)Gga>Tga | p.G303* |
LUSC | 4 | 16504484 | 16504484 | + | Missense_Mutation | SNP | C | C | A | TCGA-56-1622-01A-01D-1521-08 | TCGA-56-1622-11A-01D-1521-08 | g.chr4:16504484C>A | c.904G>T | c.(904-906)Gta>Tta | p.V302L |
LUSC | 4 | 16510277 | 16510277 | + | Missense_Mutation | SNP | T | T | C | TCGA-39-5022-01A-21D-1817-08 | TCGA-39-5022-11A-01D-1817-08 | g.chr4:16510277T>C | c.772A>G | c.(772-774)Aga>Gga | p.R258G |
LUSC | 4 | 16510279 | 16510279 | + | Missense_Mutation | SNP | C | C | T | TCGA-66-2756-01A-01D-1522-08 | TCGA-66-2756-11A-01D-1522-08 | g.chr4:16510279C>T | c.770G>A | c.(769-771)cGg>cAg | p.R257Q |
LUSC | 4 | 16597384 | 16597384 | + | Missense_Mutation | SNP | G | G | T | TCGA-18-4083-01A-01D-1352-08 | TCGA-18-4083-11A-01D-1352-08 | g.chr4:16597384G>T | c.350C>A | c.(349-351)aCg>aAg | p.T117K |
LUSC | 4 | 16597389 | 16597389 | + | Silent | SNP | G | G | C | TCGA-85-6560-01A-11D-1817-08 | TCGA-85-6560-10A-01D-1817-08 | g.chr4:16597389G>C | c.345C>G | c.(343-345)tcC>tcG | p.S115S |
LUSC | 4 | 16900050 | 16900050 | + | Missense_Mutation | SNP | C | C | G | TCGA-46-3765-01A-01D-0983-08 | TCGA-46-3765-10A-01D-0983-08 | g.chr4:16900050C>G | c.59G>C | c.(58-60)aGg>aCg | p.R20T |
OV | 4 | 16513654 | 16513654 | + | Missense_Mutation | SNP | C | C | T | TCGA-61-2613-01A-01W-1092-09 | TCGA-61-2613-11A-01W-1092-09 | g.chr4:16513654C>T | c.689G>A | c.(688-690)tGc>tAc | p.C230Y |
PAAD | 4 | 16504390 | 16504390 | + | Missense_Mutation | SNP | C | C | T | TCGA-3A-A9IC-01A-11D-A38G-08 | TCGA-3A-A9IC-10A-01D-A38J-08 | g.chr4:16504390C>T | c.998G>A | c.(997-999)gGc>gAc | p.G333D |
PAAD | 4 | 16504411 | 16504411 | + | Missense_Mutation | SNP | G | G | A | TCGA-2L-AAQJ-01A-12D-A397-08 | TCGA-2L-AAQJ-11A-11D-A39A-08 | g.chr4:16504411G>A | c.977C>T | c.(976-978)aCg>aTg | p.T326M |
PRAD | 4 | 16590333 | 16590333 | + | Splice_Site | SNP | A | A | G | TCGA-HC-A6AS-01A-11D-A30E-08 | TCGA-HC-A6AS-10A-01D-A30H-08 | g.chr4:16590333A>G | c.531T>C | c.(529-531)caT>caC | p.H177H |
READ | 4 | 16597494 | 16597494 | + | Silent | SNP | G | G | A | TCGA-DC-6158-01A-11D-1657-10 | TCGA-DC-6158-10A-01D-1657-10 | g.chr4:16597494G>A | c.240C>T | c.(238-240)atC>atT | p.I80I |
READ | 4 | 16760787 | 16760787 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-AG-A002-01A-01W-A00K-09 | TCGA-AG-A002-10A-01W-A00K-09 | g.chr4:16760787G>A | c.229C>T | c.(229-231)Cga>Tga | p.R77* |
SKCM | 4 | 16504280 | 16504280 | + | Nonsense_Mutation | SNP | G | G | A | TCGA-GN-A268-06A-11D-A196-08 | TCGA-GN-A268-10A-01D-A198-08 | g.chr4:16504280G>A | c.1108C>T | c.(1108-1110)Cag>Tag | p.Q370* |
SKCM | 4 | 16504332 | 16504332 | + | Nonsense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr4:16504332C>T | c.1056G>A | c.(1054-1056)tgG>tgA | p.W352* |
SKCM | 4 | 16504337 | 16504337 | + | Missense_Mutation | SNP | G | G | A | TCGA-D9-A6EC-06A-11D-A30X-08 | TCGA-D9-A6EC-10A-01D-A30X-08 | g.chr4:16504337G>A | c.1051C>T | c.(1051-1053)Ccg>Tcg | p.P351S |
SKCM | 4 | 16510176 | 16510176 | + | Silent | SNP | A | A | G | TCGA-EE-A2GJ-06A-11D-A196-08 | TCGA-EE-A2GJ-10A-01D-A198-08 | g.chr4:16510176A>G | c.873T>C | c.(871-873)agT>agC | p.S291S |
SKCM | 4 | 16510246 | 16510246 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29R-06A-11D-A197-08 | TCGA-EE-A29R-10A-01D-A199-08 | g.chr4:16510246G>A | c.803C>T | c.(802-804)tCc>tTc | p.S268F |
SKCM | 4 | 16510260 | 16510260 | + | Silent | SNP | G | G | A | TCGA-D3-A2JD-06A-11D-A19A-08 | TCGA-D3-A2JD-10A-01D-A19A-08 | g.chr4:16510260G>A | c.789C>T | c.(787-789)tcC>tcT | p.S263S |
SKCM | 4 | 16510261 | 16510261 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A3JD-06A-11D-A20D-08 | TCGA-EE-A3JD-10A-01D-A20D-08 | g.chr4:16510261G>A | c.788C>T | c.(787-789)tCc>tTc | p.S263F |
SKCM | 4 | 16510278 | 16510278 | + | Silent | SNP | C | C | T | TCGA-EE-A2MJ-06A-11D-A197-08 | TCGA-EE-A2MJ-10A-01D-A199-08 | g.chr4:16510278C>T | c.771G>A | c.(769-771)cgG>cgA | p.R257R |
SKCM | 4 | 16510279 | 16510279 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2GJ-06A-11D-A196-08 | TCGA-EE-A2GJ-10A-01D-A198-08 | g.chr4:16510279C>T | c.770G>A | c.(769-771)cGg>cAg | p.R257Q |
SKCM | 4 | 16513650 | 16513650 | + | Silent | SNP | C | C | T | TCGA-EE-A29S-06A-11D-A197-08 | TCGA-EE-A29S-10A-01D-A199-08 | g.chr4:16513650C>T | c.693G>A | c.(691-693)ctG>ctA | p.L231L |
SKCM | 4 | 16513672 | 16513672 | + | Missense_Mutation | SNP | T | T | C | TCGA-GF-A6C9-06A-11D-A30X-08 | TCGA-GF-A6C9-10A-01D-A30X-08 | g.chr4:16513672T>C | c.671A>G | c.(670-672)aAc>aGc | p.N224S |
SKCM | 4 | 16590354 | 16590354 | + | Silent | SNP | C | C | T | TCGA-EE-A2MS-06A-11D-A197-08 | TCGA-EE-A2MS-10A-01D-A199-08 | g.chr4:16590354C>T | c.510G>A | c.(508-510)ccG>ccA | p.P170P |
SKCM | 4 | 16597413 | 16597413 | + | Silent | SNP | C | C | T | TCGA-OD-A75X-06A-12D-A32N-08 | TCGA-OD-A75X-10A-01D-A32N-08 | g.chr4:16597413C>T | c.321G>A | c.(319-321)tcG>tcA | p.S107S |
SKCM | 4 | 16597450 | 16597450 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A29M-06A-11D-A196-08 | TCGA-EE-A29M-10A-01D-A198-08 | g.chr4:16597450C>T | c.284G>A | c.(283-285)gGa>gAa | p.G95E |
SKCM | 4 | 16597475 | 16597475 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A29E-06A-11D-A197-08 | TCGA-EE-A29E-10A-01D-A199-08 | g.chr4:16597475G>A | c.259C>T | c.(259-261)Cgt>Tgt | p.R87C |
SKCM | 4 | 16597476 | 16597476 | + | Silent | SNP | G | G | A | TCGA-EE-A29E-06A-11D-A197-08 | TCGA-EE-A29E-10A-01D-A199-08 | g.chr4:16597476G>A | c.258C>T | c.(256-258)ccC>ccT | p.P86P |
SKCM | 4 | 16760786 | 16760786 | + | Missense_Mutation | SNP | C | C | T | TCGA-EE-A2MC-06A-12D-A197-08 | TCGA-EE-A2MC-10A-01D-A199-08 | g.chr4:16760786C>T | c.230G>A | c.(229-231)cGa>cAa | p.R77Q |
SKCM | 4 | 16760838 | 16760838 | + | Missense_Mutation | SNP | C | C | T | TCGA-FW-A3R5-06A-11D-A23B-08 | TCGA-FW-A3R5-10A-01D-A23B-08 | g.chr4:16760838C>T | c.178G>A | c.(178-180)Gaa>Aaa | p.E60K |
SKCM | 4 | 16760851 | 16760851 | + | Silent | SNP | G | G | A | TCGA-FS-A1ZS-06A-12D-A197-08 | TCGA-FS-A1ZS-10A-01D-A199-08 | g.chr4:16760851G>A | c.165C>T | c.(163-165)gcC>gcT | p.A55A |
SKCM | 4 | 16760876 | 16760876 | + | Missense_Mutation | SNP | T | T | G | TCGA-EE-A2MU-06A-21D-A196-08 | TCGA-EE-A2MU-10A-01D-A198-08 | g.chr4:16760876T>G | c.140A>C | c.(139-141)gAc>gCc | p.D47A |
SKCM | 4 | 16900017 | 16900017 | + | Missense_Mutation | SNP | C | C | T | TCGA-RP-A695-06A-11D-A30X-08 | TCGA-RP-A695-10A-01D-A30X-08 | g.chr4:16900017C>T | c.92G>A | c.(91-93)cGa>cAa | p.R31Q |
SKCM | 4 | 16900071 | 16900071 | + | Missense_Mutation | SNP | G | G | A | TCGA-EE-A181-06A-11D-A196-08 | TCGA-EE-A181-10A-01D-A198-08 | g.chr4:16900071G>A | c.38C>T | c.(37-39)cCt>cTt | p.P13L |