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 36891628 36891628 + Missense_Mutation SNP T T G TCGA-OR-A5JW-01A-11D-A29I-10 TCGA-OR-A5JW-10A-01D-A29L-10 g.chr17:36891628T>G c.883A>C c.(883-885)Acc>Ccc p.T295P BLCA 17 36894649 36894649 + Missense_Mutation SNP G G C TCGA-SY-A9G5-01A-11D-A38G-08 TCGA-SY-A9G5-10A-01D-A38J-08 g.chr17:36894649G>C c.533C>G c.(532-534)gCc>gGc p.A178G BLCA 17 36894838 36894838 + Missense_Mutation SNP C C G TCGA-ZF-A9RG-01A-21D-A42E-08 TCGA-ZF-A9RG-10A-01D-A42H-08 g.chr17:36894838C>G c.436G>C c.(436-438)Gag>Cag p.E146Q BLCA 17 36894838 36894838 + Missense_Mutation SNP C C T TCGA-GU-AATP-01A-11D-A391-08 TCGA-GU-AATP-10A-01D-A394-08 g.chr17:36894838C>T c.436G>A c.(436-438)Gag>Aag p.E146K BLCA 17 36895052 36895052 + Missense_Mutation SNP C C T TCGA-SY-A9G5-01A-11D-A38G-08 TCGA-SY-A9G5-10A-01D-A38J-08 g.chr17:36895052C>T c.379G>A c.(379-381)Gat>Aat p.D127N BLCA 17 36895328 36895328 + Silent SNP C C A TCGA-4Z-AA80-01A-11D-A391-08 TCGA-4Z-AA80-10A-01D-A394-08 g.chr17:36895328C>A c.309G>T c.(307-309)ctG>ctT p.L103L BRCA 17 36895346 36895346 + Missense_Mutation SNP G G T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr17:36895346G>T c.291C>A c.(289-291)ttC>ttA p.F97L COAD 17 36891671 36891675 + Frame_Shift_Del DEL GGCTG GGCTG - TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr17:36891671_36891675delGGCTG c.836_840delCAGCC c.(835-840)ccagccfs p.PA279fs COAD 17 36891728 36891730 + In_Frame_Del DEL GTC GTC - TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr17:36891728_36891730delGTC c.781_783delGAC c.(781-783)gacdel p.D261del COAD 17 36891758 36891758 + Silent SNP G G A TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr17:36891758G>A c.753C>T c.(751-753)agC>agT p.S251S COAD 17 36895085 36895085 + Missense_Mutation SNP C C T TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr17:36895085C>T c.346G>A c.(346-348)Gag>Aag p.E116K COAD 17 36895359 36895359 + Missense_Mutation SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr17:36895359C>T c.278G>A c.(277-279)cGg>cAg p.R93Q COAD 17 36895838 36895838 + Splice_Site SNP C C T TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr17:36895838C>T c.e5+1 COAD 17 36896587 36896587 + Frame_Shift_Del DEL C C - TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr17:36896587delC c.69delG c.(67-69)gggfs p.G23fs COADREAD 17 36891671 36891675 + Frame_Shift_Del DEL GGCTG GGCTG - TCGA-AD-5900-01A-11D-1650-10 TCGA-AD-5900-10A-01D-1650-10 g.chr17:36891671_36891675delGGCTG c.836_840delCAGCC c.(835-840)ccagccfs p.PA279fs COADREAD 17 36891728 36891730 + In_Frame_Del DEL GTC GTC - TCGA-D5-6540-01A-11D-1719-10 TCGA-D5-6540-10A-01D-1719-10 g.chr17:36891728_36891730delGTC c.781_783delGAC c.(781-783)gacdel p.D261del COADREAD 17 36891758 36891758 + Silent SNP G G A TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr17:36891758G>A c.753C>T c.(751-753)agC>agT p.S251S COADREAD 17 36895085 36895085 + Missense_Mutation SNP C C T TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr17:36895085C>T c.346G>A c.(346-348)Gag>Aag p.E116K COADREAD 17 36895359 36895359 + Missense_Mutation SNP C C T TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr17:36895359C>T c.278G>A c.(277-279)cGg>cAg p.R93Q COADREAD 17 36895838 36895838 + Splice_Site SNP C C T TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr17:36895838C>T c.e5+1 COADREAD 17 36895857 36895857 + Missense_Mutation SNP C C T TCGA-DC-6160-01A-11D-1657-10 TCGA-DC-6160-10A-01D-1657-10 g.chr17:36895857C>T c.191G>A c.(190-192)cGg>cAg p.R64Q COADREAD 17 36895858 36895858 + Missense_Mutation SNP G G A TCGA-AG-3731-01A-11D-1733-10 TCGA-AG-3731-11A-01D-1733-10 g.chr17:36895858G>A c.190C>T c.(190-192)Cgg>Tgg p.R64W COADREAD 17 36896587 36896587 + Frame_Shift_Del DEL C C - TCGA-CM-6162-01A-11D-1650-10 TCGA-CM-6162-10A-01D-1650-10 g.chr17:36896587delC c.69delG c.(67-69)gggfs p.G23fs ESCA 17 36891779 36891779 + Silent SNP G G C TCGA-XP-A8T6-01A-11D-A36J-09 TCGA-XP-A8T6-10A-01D-A36M-09 g.chr17:36891779G>C c.732C>G c.(730-732)ccC>ccG p.P244P ESCA 17 36892358 36892358 + Frame_Shift_Del DEL G G - TCGA-XP-A8T7-01A-11D-A36J-09 TCGA-XP-A8T7-10A-01D-A36M-09 g.chr17:36892358delG c.642delC c.(640-642)atcfs p.I214fs ESCA 17 36892390 36892391 + Missense_Mutation DNP CC CC TA TCGA-L5-A88V-01A-11D-A351-09 TCGA-L5-A88V-11A-11D-A351-09 g.chr17:36892390_36892391CC>TA c.609_610GG>TA c.(607-612)aaGGaa>aaTAaa p.203_204KE>NK HNSC 17 36896596 36896596 + Silent SNP G G A TCGA-MT-A67F-01A-11D-A30E-08 TCGA-MT-A67F-10A-01D-A30H-08 g.chr17:36896596G>A c.60C>T c.(58-60)ctC>ctT p.L20L KIPAN 17 36891478 36891482 + Stop_Codon_Del DEL AAGTT AAGTT - TCGA-5P-A9JY-01A-11D-A42J-10 TCGA-5P-A9JY-10A-01D-A42M-10 g.chr17:36891478_36891482delAAGTT KIPAN 17 36891741 36891741 + Missense_Mutation SNP T T C TCGA-IA-A83W-01A-11D-A34Z-10 TCGA-IA-A83W-11A-11D-A34Z-10 g.chr17:36891741T>C c.770A>G c.(769-771)gAg>gGg p.E257G KIPAN 17 36892363 36892363 + Missense_Mutation SNP A A T TCGA-A3-3358-01A-01D-1534-10 TCGA-A3-3358-11A-01D-1534-10 g.chr17:36892363A>T c.637T>A c.(637-639)Tac>Aac p.Y213N KIPAN 17 36895856 36895856 + Silent SNP C C T TCGA-B0-4843-01A-01D-1361-10 TCGA-B0-4843-11A-01D-1361-10 g.chr17:36895856C>T c.192G>A c.(190-192)cgG>cgA p.R64R KIRC 17 36892363 36892363 + Missense_Mutation SNP A A T TCGA-A3-3358-01A-01D-1534-10 TCGA-A3-3358-11A-01D-1534-10 g.chr17:36892363A>T c.637T>A c.(637-639)Tac>Aac p.Y213N KIRC 17 36895856 36895856 + Silent SNP C C T TCGA-B0-4843-01A-01D-1361-10 TCGA-B0-4843-11A-01D-1361-10 g.chr17:36895856C>T c.192G>A c.(190-192)cgG>cgA p.R64R KIRP 17 36891478 36891482 + Stop_Codon_Del DEL AAGTT AAGTT - TCGA-5P-A9JY-01A-11D-A42J-10 TCGA-5P-A9JY-10A-01D-A42M-10 g.chr17:36891478_36891482delAAGTT KIRP 17 36891741 36891741 + Missense_Mutation SNP T T C TCGA-IA-A83W-01A-11D-A34Z-10 TCGA-IA-A83W-11A-11D-A34Z-10 g.chr17:36891741T>C c.770A>G c.(769-771)gAg>gGg p.E257G LIHC 17 36891668 36891668 + Silent SNP G G T TCGA-UB-A7MB-01A-11D-A33Q-10 TCGA-UB-A7MB-10A-01D-A33Q-10 g.chr17:36891668G>T c.843C>A c.(841-843)acC>acA p.T281T LIHC 17 36891702 36891702 + Missense_Mutation SNP G G A TCGA-DD-A1EL-01A-11D-A152-10 TCGA-DD-A1EL-10A-01D-A152-10 g.chr17:36891702G>A c.809C>T c.(808-810)cCa>cTa p.P270L LIHC 17 36891838 36891838 + Frame_Shift_Del DEL G G - TCGA-G3-A3CJ-01A-11D-A20W-10 TCGA-G3-A3CJ-10A-01D-A20W-10 g.chr17:36891838delG c.673delC c.(673-675)ctcfs p.L225fs LUAD 17 36894636 36894636 + Silent SNP G G A TCGA-55-6982-01A-11D-1945-08 TCGA-55-6982-11A-01D-1945-08 g.chr17:36894636G>A c.546C>T c.(544-546)cgC>cgT p.R182R LUAD 17 36895068 36895070 + In_Frame_Del DEL CTC CTC - TCGA-69-A59K-01A-11D-A25L-08 TCGA-69-A59K-10A-01D-A25L-08 g.chr17:36895068_36895070delCTC c.361_363delGAG c.(361-363)gagdel p.E121del LUAD 17 36895085 36895085 + Missense_Mutation SNP C C T TCGA-95-7947-01A-11D-2184-08 TCGA-95-7947-10A-01D-2184-08 g.chr17:36895085C>T c.346G>A c.(346-348)Gag>Aag p.E116K LUAD 17 36895840 36895840 + Splice_Site SNP T T A TCGA-50-5044-01A-21D-1855-08 TCGA-50-5044-10A-01D-1855-08 g.chr17:36895840T>A c.208A>T c.(208-210)Agg>Tgg p.R70W LUAD 17 36895846 36895846 + Missense_Mutation SNP T T C TCGA-50-5044-01A-21D-1855-08 TCGA-50-5044-10A-01D-1855-08 g.chr17:36895846T>C c.202A>G c.(202-204)Agc>Ggc p.S68G LUAD 17 36896586 36896587 + Frame_Shift_Ins INS - - C TCGA-17-Z041-01A-01W-0746-08 TCGA-17-Z041-11A-01W-0746-08 g.chr17:36896586_36896587insC c.69_70insG c.(67-72)gggtacfs p.Y24fs LUAD 17 36896596 36896596 + Silent SNP G G C TCGA-17-Z057-01A-01W-0747-08 TCGA-17-Z057-11A-01W-0747-08 g.chr17:36896596G>C c.60C>G c.(58-60)ctC>ctG p.L20L OV 17 36891700 36891700 + Missense_Mutation SNP C C G TCGA-42-2589-01A-01D-1526-09 TCGA-42-2589-10A-01D-1526-09 g.chr17:36891700C>G c.811G>C c.(811-813)Gcc>Ccc p.A271P PRAD 17 36895857 36895857 + Missense_Mutation SNP C C T TCGA-J9-A52C-01A-11D-A26M-08 TCGA-J9-A52C-10A-01D-A26K-08 g.chr17:36895857C>T c.191G>A c.(190-192)cGg>cAg p.R64Q READ 17 36895857 36895857 + Missense_Mutation SNP C C T TCGA-DC-6160-01A-11D-1657-10 TCGA-DC-6160-10A-01D-1657-10 g.chr17:36895857C>T c.191G>A c.(190-192)cGg>cAg p.R64Q READ 17 36895858 36895858 + Missense_Mutation SNP G G A TCGA-AG-3731-01A-11D-1733-10 TCGA-AG-3731-11A-01D-1733-10 g.chr17:36895858G>A c.190C>T c.(190-192)Cgg>Tgg p.R64W SKCM 17 36894641 36894641 + Missense_Mutation SNP G G A TCGA-FS-A1YY-06A-11D-A197-08 TCGA-FS-A1YY-10A-01D-A199-08 g.chr17:36894641G>A c.541C>T c.(541-543)Ctc>Ttc p.L181F SKCM 17 36894823 36894823 + Silent SNP G G A TCGA-FS-A1ZA-06A-11D-A197-08 TCGA-FS-A1ZA-10A-01D-A199-08 g.chr17:36894823G>A c.451C>T c.(451-453)Ctg>Ttg p.L151L SKCM 17 36895320 36895320 + Splice_Site SNP C C T TCGA-DA-A3F5-06A-11D-A20D-08 TCGA-DA-A3F5-10A-01D-A20D-08 g.chr17:36895320C>T c.e7+1 SKCM 17 36896591 36896591 + Missense_Mutation SNP C C T TCGA-EE-A2GC-06A-11D-A197-08 TCGA-EE-A2GC-10A-01D-A199-08 g.chr17:36896591C>T c.65G>A c.(64-66)gGg>gAg p.G22E SKCM 17 36896592 36896592 + Missense_Mutation SNP C C T TCGA-EE-A2GC-06A-11D-A197-08 TCGA-EE-A2GC-10A-01D-A199-08 g.chr17:36896592C>T c.64G>A c.(64-66)Ggg>Agg p.G22R SKCM 17 36896631 36896631 + Missense_Mutation SNP T T G TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr17:36896631T>G c.25A>C c.(25-27)Atc>Ctc p.I9L

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.371614;Hs.371617 17q12 600346

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A T Missense p.Y213N c.637T>A 17 36892363 RCCC C A Missense p.G156W c.466G>T 17 36894808 BRCA CC TT Missense p.G22E c.65_66delinsAA 17 36896590 THCA CC TT Missense p.G22K c.64_65delinsAA 17 36896591 CM C T Missense p.D128N c.382G>A 17 36895049 BRCA C T Missense p.D143N c.427G>A 17 36894847 BRCA C T Missense p.D155N c.463G>A 17 36894811 BRCA C T Missense p.E136K c.406G>A 17 36895025 BRCA C T Missense p.E146K c.436G>A 17 36894838 BRCA C T Missense p.E246K c.736G>A 17 36891775 BRCA C T Missense p.R64W c.190C>T 17 36895858 GBM C T SpliceDonorSNV . c.316+1G>A 17 36895320 CM C T Synonymous p.R64R c.192G>A 17 36895856 RCCC G A Missense p.L181F c.541C>T 17 36894641 CM G A Missense p.R64W c.190C>T 17 36895858 THCA G A Synonymous p.C21C c.63C>T 17 36896593 STAD G A Synonymous p.L151L c.451C>T 17 36894823 CM G C Synonymous p.L20L c.60C>G 17 36896596 LUAD G T Synonymous p.P302P c.906C>A 17 36891605 CM T A Missense p.R70W c.208A>T 17 36895840 LUAD T C Missense p.S68G c.202A>G 17 36895846 LUAD TGTCT - Frameshift p.Q76Hfs*11 c.228_232delAGACA 17 36895484 BRCA