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 17 36508662 36508663 + In_Frame_Ins INS - - AGC TCGA-OR-A5J6-01A-31D-A29I-10 TCGA-OR-A5J6-10A-01D-A29L-10 g.chr17:36508662_36508663insAGC c.535_536insAGC c.(535-537)gag>gAGCag p.187_188insQ BLCA 17 36508816 36508816 + Missense_Mutation SNP G G A TCGA-FD-A6TH-01A-11D-A32B-08 TCGA-FD-A6TH-10A-01D-A329-08 g.chr17:36508816G>A c.689G>A c.(688-690)gGg>gAg p.G230E BLCA 17 36522182 36522182 + Missense_Mutation SNP G G C TCGA-FD-A6TG-01A-11D-A32B-08 TCGA-FD-A6TG-10A-01D-A329-08 g.chr17:36522182G>C c.1073G>C c.(1072-1074)cGg>cCg p.R358P BLCA 17 36522197 36522197 + Missense_Mutation SNP G G A TCGA-4Z-AA80-01A-11D-A391-08 TCGA-4Z-AA80-10A-01D-A394-08 g.chr17:36522197G>A c.1088G>A c.(1087-1089)cGa>cAa p.R363Q BLCA 17 36522286 36522286 + Nonsense_Mutation SNP C C T TCGA-KQ-A41R-01A-21D-A34U-08 TCGA-KQ-A41R-10G-01D-A34X-08 g.chr17:36522286C>T c.1177C>T c.(1177-1179)Cga>Tga p.R393* BLCA 17 36523815 36523815 + Silent SNP G G A TCGA-S5-A6DX-01A-11D-A31L-08 TCGA-S5-A6DX-10A-01D-A31J-08 g.chr17:36523815G>A c.1242G>A c.(1240-1242)ctG>ctA p.L414L BLCA 17 36523881 36523881 + Silent SNP C C T TCGA-G2-A3VY-01A-11D-A22Z-08 TCGA-G2-A3VY-10A-01D-A22Z-08 g.chr17:36523881C>T c.1308C>T c.(1306-1308)ctC>ctT p.L436L BLCA 17 36551570 36551570 + Frame_Shift_Del DEL C C - TCGA-BT-A2LB-01A-11D-A18F-08 TCGA-BT-A2LB-10A-01D-A18F-08 g.chr17:36551570delC c.1498delC c.(1498-1500)ccafs p.P500fs BRCA 17 36508490 36508490 + Silent SNP A A G TCGA-AR-A1AT-01A-11D-A12Q-09 TCGA-AR-A1AT-10A-01D-A12Q-09 g.chr17:36508490A>G c.363A>G c.(361-363)gaA>gaG p.E121E BRCA 17 36522192 36522192 + Silent SNP C C T TCGA-A2-A0CU-01A-12W-A050-09 TCGA-A2-A0CU-10A-01W-A055-09 g.chr17:36522192C>T c.1083C>T c.(1081-1083)ccC>ccT p.P361P CESC 17 36521234 36521234 + Silent SNP G G A TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr17:36521234G>A c.1002G>A c.(1000-1002)ccG>ccA p.P334P CESC 17 36521268 36521268 + Missense_Mutation SNP C C T TCGA-IR-A3LA-01A-11D-A22X-09 TCGA-IR-A3LA-10A-01D-A22X-09 g.chr17:36521268C>T c.1036C>T c.(1036-1038)Ccg>Tcg p.P346S COAD 17 36508581 36508581 + Missense_Mutation SNP C C A TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr17:36508581C>A c.454C>A c.(454-456)Ctg>Atg p.L152M COAD 17 36521264 36521264 + Silent SNP A A C TCGA-AA-3861-01A-01W-0995-10 TCGA-AA-3861-10A-01W-0995-10 g.chr17:36521264A>C c.1032A>C c.(1030-1032)ctA>ctC p.L344L COADREAD 17 36508581 36508581 + Missense_Mutation SNP C C A TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr17:36508581C>A c.454C>A c.(454-456)Ctg>Atg p.L152M COADREAD 17 36508688 36508688 + Silent SNP A A G TCGA-DC-5869-01A-01D-1657-10 TCGA-DC-5869-10A-01D-1657-10 g.chr17:36508688A>G c.561A>G c.(559-561)caA>caG p.Q187Q COADREAD 17 36521264 36521264 + Silent SNP A A C TCGA-AA-3861-01A-01W-0995-10 TCGA-AA-3861-10A-01W-0995-10 g.chr17:36521264A>C c.1032A>C c.(1030-1032)ctA>ctC p.L344L HNSC 17 36508743 36508743 + Frame_Shift_Del DEL C C - TCGA-CN-6010-01A-11D-1683-08 TCGA-CN-6010-10A-01D-1683-08 g.chr17:36508743delC c.616delC c.(616-618)cggfs p.R206fs HNSC 17 36520668 36520668 + Missense_Mutation SNP C C G TCGA-CV-5432-01A-02D-1683-08 TCGA-CV-5432-10A-01D-1870-08 g.chr17:36520668C>G c.887C>G c.(886-888)tCt>tGt p.S296C HNSC 17 36552194 36552194 + Silent SNP G G A TCGA-CR-7365-01A-11D-2012-08 TCGA-CR-7365-10A-01D-2013-08 g.chr17:36552194G>A c.1719G>A c.(1717-1719)caG>caA p.Q573Q KICH 17 36520640 36520640 + Missense_Mutation SNP A A G TCGA-KL-8323-01A-21D-2310-10 TCGA-KL-8323-11A-01D-2310-10 g.chr17:36520640A>G c.859A>G c.(859-861)Act>Gct p.T287A KICH 17 36521270 36521270 + Silent SNP G G A TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr17:36521270G>A c.1038G>A c.(1036-1038)ccG>ccA p.P346P KICH 17 36552111 36552111 + Missense_Mutation SNP T T C TCGA-KL-8342-01A-11D-2310-10 TCGA-KL-8342-11A-01D-2310-10 g.chr17:36552111T>C c.1636T>C c.(1636-1638)Tct>Cct p.S546P KIPAN 17 36508826 36508826 + Silent SNP C C A TCGA-HE-A5NF-01A-11D-A26P-10 TCGA-HE-A5NF-10A-01D-A26P-10 g.chr17:36508826C>A c.699C>A c.(697-699)acC>acA p.T233T KIPAN 17 36520640 36520640 + Missense_Mutation SNP A A G TCGA-KL-8323-01A-21D-2310-10 TCGA-KL-8323-11A-01D-2310-10 g.chr17:36520640A>G c.859A>G c.(859-861)Act>Gct p.T287A KIPAN 17 36521270 36521270 + Silent SNP G G A TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr17:36521270G>A c.1038G>A c.(1036-1038)ccG>ccA p.P346P KIPAN 17 36523827 36523827 + Silent SNP A A G TCGA-CW-5581-01A-02D-1534-10 TCGA-CW-5581-11A-01D-1535-10 g.chr17:36523827A>G c.1254A>G c.(1252-1254)ccA>ccG p.P418P KIPAN 17 36552111 36552111 + Missense_Mutation SNP T T C TCGA-KL-8342-01A-11D-2310-10 TCGA-KL-8342-11A-01D-2310-10 g.chr17:36552111T>C c.1636T>C c.(1636-1638)Tct>Cct p.S546P KIRC 17 36523827 36523827 + Silent SNP A A G TCGA-CW-5581-01A-02D-1534-10 TCGA-CW-5581-11A-01D-1535-10 g.chr17:36523827A>G c.1254A>G c.(1252-1254)ccA>ccG p.P418P KIRP 17 36508826 36508826 + Silent SNP C C A TCGA-HE-A5NF-01A-11D-A26P-10 TCGA-HE-A5NF-10A-01D-A26P-10 g.chr17:36508826C>A c.699C>A c.(697-699)acC>acA p.T233T LIHC 17 36508355 36508355 + Silent SNP C C T TCGA-G3-A6UC-01A-21D-A33K-10 TCGA-G3-A6UC-10A-01D-A33K-10 g.chr17:36508355C>T c.228C>T c.(226-228)gtC>gtT p.V76V LIHC 17 36508540 36508541 + Missense_Mutation DNP GC GC AG TCGA-5C-A9VH-01A-11D-A36X-10 TCGA-5C-A9VH-10A-01D-A370-10 g.chr17:36508540_36508541GC>AG c.413_414GC>AG c.(412-414)aGC>aAG p.S138K LUAD 17 36520738 36520738 + Splice_Site SNP A A G TCGA-86-A4JF-01A-11D-A24P-08 TCGA-86-A4JF-10A-01D-A24P-08 g.chr17:36520738A>G c.957A>G c.(955-957)ctA>ctG p.L319L LUAD 17 36521190 36521190 + Splice_Site SNP G G C TCGA-55-8204-01A-11D-2238-08 TCGA-55-8204-10A-01D-2238-08 g.chr17:36521190G>C c.e4-1 READ 17 36508688 36508688 + Silent SNP A A G TCGA-DC-5869-01A-01D-1657-10 TCGA-DC-5869-10A-01D-1657-10 g.chr17:36508688A>G c.561A>G c.(559-561)caA>caG p.Q187Q SKCM 17 36520712 36520712 + Missense_Mutation SNP C C T TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr17:36520712C>T c.931C>T c.(931-933)Cct>Tct p.P311S SKCM 17 36521269 36521269 + Missense_Mutation SNP C C T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr17:36521269C>T c.1037C>T c.(1036-1038)cCg>cTg p.P346L SKCM 17 36521280 36521280 + Missense_Mutation SNP C C T TCGA-FS-A1Z3-06A-11D-A197-08 TCGA-FS-A1Z3-10A-01D-A199-08 g.chr17:36521280C>T c.1048C>T c.(1048-1050)Ccc>Tcc p.P350S SKCM 17 36521282 36521282 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr17:36521282C>T c.1050C>T c.(1048-1050)ccC>ccT p.P350P SKCM 17 36522283 36522283 + Missense_Mutation SNP C C T TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr17:36522283C>T c.1174C>T c.(1174-1176)Ctt>Ttt p.L392F SKCM 17 36551576 36551576 + Missense_Mutation SNP C C T TCGA-QB-A6FS-06A-11D-A30X-08 TCGA-QB-A6FS-10A-01D-A30X-08 g.chr17:36551576C>T c.1504C>T c.(1504-1506)Cct>Tct p.P502S

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.514132 17q12 608788

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.K486Q c.1456A>C 17 36533635 UCEC AGC - InFrameDeletion p.Q187delQ c.558_560delGCA 17 36508663 HNSC A G Synonymous p.P418P c.1254A>G 17 36523827 RCCC A T 3-UTRSNV . c.1743+30A>T 17 36552248 CM C - Frameshift p.P500Qfs*33 c.1499delC 17 36551570 BLCA C - Frameshift p.R206Gfs*43 c.616delC 17 36508743 HNSC C G Missense p.S296C c.887C>G 17 36520668 HNSC C G Missense p.S482C c.1445C>G 17 36533624 UCEC C T 3-UTRSNV . c.1743+13C>T 17 36552231 CM C T Missense p.L392F c.1174C>T 17 36522283 CM C T Missense p.P311S c.931C>T 17 36520712 CM C T Missense p.P334L c.1001C>T 17 36521233 UCEC C T Missense p.P350S c.1048C>T 17 36521280 CM C T Synonymous p.H481H c.1443C>T 17 36533622 CM C T Synonymous p.P361P c.1083C>T 17 36522192 BRCA G A Missense p.S370N c.1109G>A 17 36522218 STAD G A Synonymous p.Q573Q c.1719G>A 17 36552194 HNSC G T Synonymous p.L248L c.744G>T 17 36508871 STAD T C Synonymous p.R431R c.1293T>C 17 36523866 RCCC