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 1561614 1561614 + Missense_Mutation SNP C C T TCGA-OR-A5K4-01A-11D-A29I-10 TCGA-OR-A5K4-10A-01D-A29L-10 g.chr17:1561614C>T c.5438G>A c.(5437-5439)cGc>cAc p.R1813H BLCA 17 1557133 1557133 + Silent SNP G G A TCGA-K4-A54R-01A-11D-A26M-08 TCGA-K4-A54R-10A-01D-A26K-08 g.chr17:1557133G>A c.6165C>T c.(6163-6165)atC>atT p.I2055I BLCA 17 1561929 1561929 + Missense_Mutation SNP G G A TCGA-KQ-A41R-01A-21D-A34U-08 TCGA-KQ-A41R-10G-01D-A34X-08 g.chr17:1561929G>A c.5267C>T c.(5266-5268)tCt>tTt p.S1756F BLCA 17 1562039 1562039 + Silent SNP G G A TCGA-FD-A3B3-01A-12D-A202-08 TCGA-FD-A3B3-10A-01D-A202-08 g.chr17:1562039G>A c.5157C>T c.(5155-5157)ttC>ttT p.F1719F BLCA 17 1563243 1563243 + Missense_Mutation SNP G G T TCGA-E7-A541-01A-11D-A26M-08 TCGA-E7-A541-10A-01D-A26K-08 g.chr17:1563243G>T c.4838C>A c.(4837-4839)aCa>aAa p.T1613K BLCA 17 1564436 1564436 + Silent SNP G G A TCGA-G2-A3VY-01A-11D-A22Z-08 TCGA-G2-A3VY-10A-01D-A22Z-08 g.chr17:1564436G>A c.4359C>T c.(4357-4359)ttC>ttT p.F1453F BLCA 17 1564447 1564447 + Missense_Mutation SNP G G C TCGA-G2-A3VY-01A-11D-A22Z-08 TCGA-G2-A3VY-10A-01D-A22Z-08 g.chr17:1564447G>C c.4348C>G c.(4348-4350)Cag>Gag p.Q1450E BLCA 17 1564634 1564634 + Silent SNP G G A TCGA-G2-A3VY-01A-11D-A22Z-08 TCGA-G2-A3VY-10A-01D-A22Z-08 g.chr17:1564634G>A c.4269C>T c.(4267-4269)ttC>ttT p.F1423F BLCA 17 1564678 1564678 + Missense_Mutation SNP C C G TCGA-YF-AA3L-01A-11D-A38G-08 TCGA-YF-AA3L-10A-01D-A38J-08 g.chr17:1564678C>G c.4225G>C c.(4225-4227)Gaa>Caa p.E1409Q BLCA 17 1564962 1564962 + Missense_Mutation SNP G G C TCGA-G2-A3VY-01A-11D-A22Z-08 TCGA-G2-A3VY-10A-01D-A22Z-08 g.chr17:1564962G>C c.4145C>G c.(4144-4146)tCt>tGt p.S1382C BLCA 17 1576684 1576684 + Silent SNP G G T TCGA-DK-A1A3-01A-11D-A13W-08 TCGA-DK-A1A3-10A-01D-A13W-08 g.chr17:1576684G>T c.3624C>A c.(3622-3624)acC>acA p.T1208T BLCA 17 1576731 1576731 + Missense_Mutation SNP C C T TCGA-DK-A1A3-01A-11D-A13W-08 TCGA-DK-A1A3-10A-01D-A13W-08 g.chr17:1576731C>T c.3577G>A c.(3577-3579)Gag>Aag p.E1193K BLCA 17 1578986 1578986 + Missense_Mutation SNP G G A TCGA-DK-AA6S-01A-21D-A391-08 TCGA-DK-AA6S-10A-01D-A394-08 g.chr17:1578986G>A c.2800C>T c.(2800-2802)Cgc>Tgc p.R934C BLCA 17 1579345 1579345 + Silent SNP C C A TCGA-E7-A7DU-01A-11D-A32B-08 TCGA-E7-A7DU-10A-01D-A329-08 g.chr17:1579345C>A c.2556G>T c.(2554-2556)gtG>gtT p.V852V BLCA 17 1579823 1579823 + Silent SNP C C T TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr17:1579823C>T c.2364G>A c.(2362-2364)caG>caA p.Q788Q BLCA 17 1582371 1582371 + Silent SNP G G A TCGA-CF-A1HR-01A-11D-A13W-08 TCGA-CF-A1HR-10A-01D-A13W-08 g.chr17:1582371G>A c.1539C>T c.(1537-1539)ctC>ctT p.L513L BLCA 17 1582626 1582626 + Silent SNP C C T TCGA-UY-A9PF-01A-11D-A38G-08 TCGA-UY-A9PF-10A-01D-A38J-08 g.chr17:1582626C>T c.1368G>A c.(1366-1368)ctG>ctA p.L456L BLCA 17 1584858 1584858 + Missense_Mutation SNP C C G TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr17:1584858C>G c.780G>C c.(778-780)ttG>ttC p.L260F BRCA 17 1554097 1554097 + Silent SNP C C T TCGA-E2-A159-01A-11D-A10Y-09 TCGA-E2-A159-10A-01D-A110-09 g.chr17:1554097C>T c.7007G>A c.(7006-7008)tGa>tAa p.*2336* BRCA 17 1554841 1554841 + Missense_Mutation SNP C C T TCGA-D8-A1J8-01A-11D-A13L-09 TCGA-D8-A1J8-10A-01D-A13O-09 g.chr17:1554841C>T c.6517G>A c.(6517-6519)Gaa>Aaa p.E2173K BRCA 17 1557290 1557290 + Missense_Mutation SNP G G A TCGA-C8-A132-01A-31D-A10Y-09 TCGA-C8-A132-10A-01D-A110-09 g.chr17:1557290G>A c.6008C>T c.(6007-6009)aCa>aTa p.T2003I BRCA 17 1561627 1561627 + Missense_Mutation SNP T T C TCGA-C8-A1HF-01A-11D-A135-09 TCGA-C8-A1HF-10A-01D-A135-09 g.chr17:1561627T>C c.5425A>G c.(5425-5427)Atc>Gtc p.I1809V BRCA 17 1561836 1561836 + Missense_Mutation SNP C C G TCGA-GM-A2DO-01A-11D-A19Y-09 TCGA-GM-A2DO-10D-01D-A18P-09 g.chr17:1561836C>G c.5360G>C c.(5359-5361)aGa>aCa p.R1787T BRCA 17 1564332 1564332 + Missense_Mutation SNP G G A TCGA-BH-A0GZ-01A-11W-A071-09 TCGA-BH-A0GZ-10A-01W-A071-09 g.chr17:1564332G>A c.4463C>T c.(4462-4464)aCa>aTa p.T1488I BRCA 17 1564924 1564924 + Missense_Mutation SNP C C G TCGA-C8-A1HM-01A-12D-A135-09 TCGA-C8-A1HM-10A-01D-A135-09 g.chr17:1564924C>G c.4183G>C c.(4183-4185)Gag>Cag p.E1395Q BRCA 17 1576724 1576724 + Missense_Mutation SNP C C T TCGA-EW-A1P6-01A-11D-A142-09 TCGA-EW-A1P6-10A-01D-A142-09 g.chr17:1576724C>T c.3584G>A c.(3583-3585)cGc>cAc p.R1195H BRCA 17 1577787 1577787 + Missense_Mutation SNP T T G TCGA-A2-A0T5-01A-21D-A099-09 TCGA-A2-A0T5-10A-01D-A099-09 g.chr17:1577787T>G c.3248A>C c.(3247-3249)cAc>cCc p.H1083P BRCA 17 1578489 1578489 + Missense_Mutation SNP G G A TCGA-C8-A12T-01A-11D-A10Y-09 TCGA-C8-A12T-10A-01D-A110-09 g.chr17:1578489G>A c.3017C>T c.(3016-3018)gCc>gTc p.A1006V BRCA 17 1579900 1579900 + Nonsense_Mutation SNP G G A TCGA-BH-A18G-01A-11D-A12B-09 TCGA-BH-A18G-10A-01D-A12B-09 g.chr17:1579900G>A c.2287C>T c.(2287-2289)Cga>Tga p.R763* BRCA 17 1579939 1579939 + Missense_Mutation SNP A A C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr17:1579939A>C c.2248T>G c.(2248-2250)Tgg>Ggg p.W750G BRCA 17 1580872 1580872 + Silent SNP G G T TCGA-AO-A128-01A-11D-A10M-09 TCGA-AO-A128-10A-01D-A10M-09 g.chr17:1580872G>T c.1971C>A c.(1969-1971)gcC>gcA p.A657A BRCA 17 1580966 1580966 + Missense_Mutation SNP C C A TCGA-A8-A095-01A-11W-A019-09 TCGA-A8-A095-10A-01W-A021-09 g.chr17:1580966C>A c.1877G>T c.(1876-1878)gGc>gTc p.G626V BRCA 17 1582137 1582137 + Silent SNP C C T TCGA-A2-A25B-01A-11D-A167-09 TCGA-A2-A25B-10A-01D-A167-09 g.chr17:1582137C>T c.1638G>A c.(1636-1638)ctG>ctA p.L546L CESC 17 1554817 1554817 + Missense_Mutation SNP G G C TCGA-IR-A3LH-01A-21D-A20U-09 TCGA-IR-A3LH-10A-01D-A20U-09 g.chr17:1554817G>C c.6541C>G c.(6541-6543)Cag>Gag p.Q2181E CESC 17 1554945 1554945 + Silent SNP G G C TCGA-IR-A3LH-01A-21D-A20U-09 TCGA-IR-A3LH-10A-01D-A20U-09 g.chr17:1554945G>C c.6507C>G c.(6505-6507)ctC>ctG p.L2169L CESC 17 1556852 1556852 + Missense_Mutation SNP G G C TCGA-C5-A1BQ-01C-11D-A20U-09 TCGA-C5-A1BQ-10A-01D-A20U-09 g.chr17:1556852G>C c.6353C>G c.(6352-6354)tCt>tGt p.S2118C CESC 17 1556890 1556890 + Silent SNP G G A TCGA-EK-A2R8-01A-21D-A18J-09 TCGA-EK-A2R8-10A-01D-A18J-09 g.chr17:1556890G>A c.6315C>T c.(6313-6315)atC>atT p.I2105I CESC 17 1557268 1557268 + Silent SNP G G A TCGA-EK-A2R8-01A-21D-A18J-09 TCGA-EK-A2R8-10A-01D-A18J-09 g.chr17:1557268G>A c.6030C>T c.(6028-6030)atC>atT p.I2010I CESC 17 1558693 1558693 + Missense_Mutation SNP C C T TCGA-DG-A2KK-01A-11D-A17W-09 TCGA-DG-A2KK-10A-01D-A17W-09 g.chr17:1558693C>T c.5938G>A c.(5938-5940)Gag>Aag p.E1980K CESC 17 1560004 1560004 + Missense_Mutation SNP G G A TCGA-FU-A770-01A-11D-A33O-09 TCGA-FU-A770-10A-01D-A33O-09 g.chr17:1560004G>A c.5557C>T c.(5557-5559)Cct>Tct p.P1853S CESC 17 1561948 1561948 + Missense_Mutation SNP C C G TCGA-C5-A2LX-01A-11D-A18J-09 TCGA-C5-A2LX-10A-01D-A18J-09 g.chr17:1561948C>G c.5248G>C c.(5248-5250)Ggg>Cgg p.G1750R COAD 17 1557119 1557119 + Missense_Mutation SNP C C G TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr17:1557119C>G c.6179G>C c.(6178-6180)aGc>aCc p.S2060T COAD 17 1557246 1557246 + Missense_Mutation SNP C C T TCGA-AA-3821-01A-01W-0995-10 TCGA-AA-3821-10A-01W-0995-10 g.chr17:1557246C>T c.6052G>A c.(6052-6054)Gca>Aca p.A2018T COAD 17 1559773 1559773 + Silent SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr17:1559773G>A c.5706C>T c.(5704-5706)ttC>ttT p.F1902F COAD 17 1559773 1559773 + Silent SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr17:1559773G>A c.5706C>T c.(5704-5706)ttC>ttT p.F1902F COAD 17 1560022 1560022 + Missense_Mutation SNP C C T TCGA-A6-3808-01A-01W-0995-10 TCGA-A6-3808-11A-01W-0995-10 g.chr17:1560022C>T c.5539G>A c.(5539-5541)Gcc>Acc p.A1847T COAD 17 1562781 1562781 + Frame_Shift_Del DEL C C - TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr17:1562781delC c.5008delG c.(5008-5010)gacfs p.D1670fs COAD 17 1563792 1563792 + Silent SNP G G A TCGA-AU-3779-01A-01D-1719-10 TCGA-AU-3779-10A-01D-1719-10 g.chr17:1563792G>A c.4719C>T c.(4717-4719)ctC>ctT p.L1573L COAD 17 1564595 1564595 + Nonsense_Mutation SNP C C T TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr17:1564595C>T c.4308G>A c.(4306-4308)tgG>tgA p.W1436* COAD 17 1564662 1564662 + Missense_Mutation SNP C C T TCGA-AA-3680-01A-01W-0900-09 TCGA-AA-3680-10A-01W-0900-09 g.chr17:1564662C>T c.4241G>A c.(4240-4242)cGt>cAt p.R1414H COAD 17 1565307 1565307 + Silent SNP G G C TCGA-AA-A02K-01A-21W-A096-10 TCGA-AA-A02K-10A-01W-A096-10 g.chr17:1565307G>C c.3915C>G c.(3913-3915)tcC>tcG p.S1305S COAD 17 1576726 1576726 + Silent SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr17:1576726G>A c.3582C>T c.(3580-3582)tgC>tgT p.C1194C COAD 17 1576820 1576820 + Missense_Mutation SNP C C T TCGA-AA-3939-01A-01W-0995-10 TCGA-AA-3939-10A-01W-0995-10 g.chr17:1576820C>T c.3488G>A c.(3487-3489)cGg>cAg p.R1163Q COAD 17 1577829 1577829 + Missense_Mutation SNP T T C TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr17:1577829T>C c.3206A>G c.(3205-3207)aAt>aGt p.N1069S COAD 17 1577960 1577960 + Silent SNP C C T TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr17:1577960C>T c.3075G>A c.(3073-3075)acG>acA p.T1025T COAD 17 1578514 1578514 + Missense_Mutation SNP G G T TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr17:1578514G>T c.2992C>A c.(2992-2994)Cgc>Agc p.R998S COAD 17 1578592 1578592 + Missense_Mutation SNP C C T TCGA-AA-3949-01A-01W-0995-10 TCGA-AA-3949-10A-01W-0995-10 g.chr17:1578592C>T c.2914G>A c.(2914-2916)Gag>Aag p.E972K COAD 17 1579070 1579070 + Missense_Mutation SNP C C T TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr17:1579070C>T c.2716G>A c.(2716-2718)Gtt>Att p.V906I COAD 17 1582908 1582908 + Missense_Mutation SNP C C A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr17:1582908C>A c.1284G>T c.(1282-1284)aaG>aaT p.K428N COAD 17 1584913 1584913 + Missense_Mutation SNP G G C TCGA-CA-6715-01A-21D-1835-10 TCGA-CA-6715-10A-01D-1835-10 g.chr17:1584913G>C c.725C>G c.(724-726)gCt>gGt p.A242G COAD 17 1584931 1584931 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr17:1584931G>A c.707C>T c.(706-708)tCg>tTg p.S236L COAD 17 1585162 1585162 + Missense_Mutation SNP G G T TCGA-AA-A01Q-01A-01W-A005-10 TCGA-AA-A01Q-10A-01W-A005-10 g.chr17:1585162G>T c.605C>A c.(604-606)cCt>cAt p.P202H COAD 17 1585473 1585473 + Frame_Shift_Del DEL G G - TCGA-AA-3680-01A-01W-0900-09 TCGA-AA-3680-10A-01W-0900-09 g.chr17:1585473delG c.384delC c.(382-384)ttcfs p.F128fs COAD 17 1586857 1586857 + Missense_Mutation SNP T T C TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr17:1586857T>C c.239A>G c.(238-240)aAg>aGg p.K80R COADREAD 17 1557119 1557119 + Missense_Mutation SNP C C G TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr17:1557119C>G c.6179G>C c.(6178-6180)aGc>aCc p.S2060T COADREAD 17 1557246 1557246 + Missense_Mutation SNP C C T TCGA-AA-3821-01A-01W-0995-10 TCGA-AA-3821-10A-01W-0995-10 g.chr17:1557246C>T c.6052G>A c.(6052-6054)Gca>Aca p.A2018T COADREAD 17 1559773 1559773 + Silent SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr17:1559773G>A c.5706C>T c.(5704-5706)ttC>ttT p.F1902F COADREAD 17 1559773 1559773 + Silent SNP G G A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr17:1559773G>A c.5706C>T c.(5704-5706)ttC>ttT p.F1902F COADREAD 17 1560022 1560022 + Missense_Mutation SNP C C T TCGA-A6-3808-01A-01W-0995-10 TCGA-A6-3808-11A-01W-0995-10 g.chr17:1560022C>T c.5539G>A c.(5539-5541)Gcc>Acc p.A1847T COADREAD 17 1562781 1562781 + Frame_Shift_Del DEL C C - TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr17:1562781delC c.5008delG c.(5008-5010)gacfs p.D1670fs COADREAD 17 1563792 1563792 + Silent SNP G G A TCGA-AU-3779-01A-01D-1719-10 TCGA-AU-3779-10A-01D-1719-10 g.chr17:1563792G>A c.4719C>T c.(4717-4719)ctC>ctT p.L1573L COADREAD 17 1564595 1564595 + Nonsense_Mutation SNP C C T TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr17:1564595C>T c.4308G>A c.(4306-4308)tgG>tgA p.W1436* COADREAD 17 1564662 1564662 + Missense_Mutation SNP C C T TCGA-AA-3680-01A-01W-0900-09 TCGA-AA-3680-10A-01W-0900-09 g.chr17:1564662C>T c.4241G>A c.(4240-4242)cGt>cAt p.R1414H COADREAD 17 1565307 1565307 + Silent SNP G G C TCGA-AA-A02K-01A-21W-A096-10 TCGA-AA-A02K-10A-01W-A096-10 g.chr17:1565307G>C c.3915C>G c.(3913-3915)tcC>tcG p.S1305S COADREAD 17 1576726 1576726 + Silent SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr17:1576726G>A c.3582C>T c.(3580-3582)tgC>tgT p.C1194C COADREAD 17 1576820 1576820 + Missense_Mutation SNP C C T TCGA-AA-3939-01A-01W-0995-10 TCGA-AA-3939-10A-01W-0995-10 g.chr17:1576820C>T c.3488G>A c.(3487-3489)cGg>cAg p.R1163Q COADREAD 17 1577829 1577829 + Missense_Mutation SNP T T C TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr17:1577829T>C c.3206A>G c.(3205-3207)aAt>aGt p.N1069S COADREAD 17 1577960 1577960 + Silent SNP C C T TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr17:1577960C>T c.3075G>A c.(3073-3075)acG>acA p.T1025T COADREAD 17 1578514 1578514 + Missense_Mutation SNP G G T TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr17:1578514G>T c.2992C>A c.(2992-2994)Cgc>Agc p.R998S COADREAD 17 1578592 1578592 + Missense_Mutation SNP C C T TCGA-AA-3949-01A-01W-0995-10 TCGA-AA-3949-10A-01W-0995-10 g.chr17:1578592C>T c.2914G>A c.(2914-2916)Gag>Aag p.E972K COADREAD 17 1579070 1579070 + Missense_Mutation SNP C C T TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr17:1579070C>T c.2716G>A c.(2716-2718)Gtt>Att p.V906I COADREAD 17 1579255 1579255 + Silent SNP C C T TCGA-AG-3594-01A-02W-0831-10 TCGA-AG-3594-10A-01W-0831-10 g.chr17:1579255C>T c.2646G>A c.(2644-2646)aaG>aaA p.K882K COADREAD 17 1582908 1582908 + Missense_Mutation SNP C C A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr17:1582908C>A c.1284G>T c.(1282-1284)aaG>aaT p.K428N COADREAD 17 1584913 1584913 + Missense_Mutation SNP G G C TCGA-CA-6715-01A-21D-1835-10 TCGA-CA-6715-10A-01D-1835-10 g.chr17:1584913G>C c.725C>G c.(724-726)gCt>gGt p.A242G COADREAD 17 1584923 1584924 + Frame_Shift_Del DEL AG AG - TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr17:1584923_1584924delAG c.714_715delCT c.(712-717)ctctacfs p.Y239fs COADREAD 17 1584931 1584931 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr17:1584931G>A c.707C>T c.(706-708)tCg>tTg p.S236L COADREAD 17 1585162 1585162 + Missense_Mutation SNP G G T TCGA-AA-A01Q-01A-01W-A005-10 TCGA-AA-A01Q-10A-01W-A005-10 g.chr17:1585162G>T c.605C>A c.(604-606)cCt>cAt p.P202H COADREAD 17 1585217 1585217 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr17:1585217C>A c.550G>T c.(550-552)Gat>Tat p.D184Y COADREAD 17 1585473 1585473 + Frame_Shift_Del DEL G G - TCGA-AA-3680-01A-01W-0900-09 TCGA-AA-3680-10A-01W-0900-09 g.chr17:1585473delG c.384delC c.(382-384)ttcfs p.F128fs COADREAD 17 1586857 1586857 + Missense_Mutation SNP T T C TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr17:1586857T>C c.239A>G c.(238-240)aAg>aGg p.K80R ESCA 17 1554764 1554764 + Missense_Mutation SNP C C A TCGA-VR-A8EX-01A-11D-A36J-09 TCGA-VR-A8EX-10A-01D-A36M-09 g.chr17:1554764C>A c.6594G>T c.(6592-6594)aaG>aaT p.K2198N ESCA 17 1561597 1561597 + Missense_Mutation SNP G G C TCGA-LN-A49M-01A-21D-A27G-09 TCGA-LN-A49M-10A-01D-A27G-09 g.chr17:1561597G>C c.5455C>G c.(5455-5457)Ctc>Gtc p.L1819V ESCA 17 1563149 1563149 + Missense_Mutation SNP C C A TCGA-JY-A93E-01A-11D-A37C-09 TCGA-JY-A93E-10A-01D-A37F-09 g.chr17:1563149C>A c.4932G>T c.(4930-4932)ttG>ttT p.L1644F ESCA 17 1564934 1564934 + Silent SNP G G C TCGA-L5-A8NS-01A-12D-A37C-09 TCGA-L5-A8NS-11A-11D-A37F-09 g.chr17:1564934G>C c.4173C>G c.(4171-4173)ctC>ctG p.L1391L ESCA 17 1582092 1582092 + Silent SNP G G A TCGA-L5-A8NM-01A-11D-A37C-09 TCGA-L5-A8NM-11A-12D-A37F-09 g.chr17:1582092G>A c.1683C>T c.(1681-1683)caC>caT p.H561H ESCA 17 1582137 1582137 + Silent SNP C C T TCGA-JY-A938-01A-11D-A37C-09 TCGA-JY-A938-10A-01D-A37F-09 g.chr17:1582137C>T c.1638G>A c.(1636-1638)ctG>ctA p.L546L ESCA 17 1582171 1582171 + Missense_Mutation SNP C C T TCGA-JY-A6FG-01A-11D-A33E-09 TCGA-JY-A6FG-10A-01D-A33H-09 g.chr17:1582171C>T c.1604G>A c.(1603-1605)aGa>aAa p.R535K ESCA 17 1586912 1586912 + Missense_Mutation SNP G G A TCGA-L5-A8NH-01A-11D-A37C-09 TCGA-L5-A8NH-11A-11D-A37F-09 g.chr17:1586912G>A c.184C>T c.(184-186)Ccc>Tcc p.P62S GBM 17 1577046 1577046 + Missense_Mutation SNP A A G TCGA-14-0790-01B-01D-1494-08 TCGA-14-0790-10A-01D-1494-08 g.chr17:1577046A>G c.3440T>C c.(3439-3441)gTt>gCt p.V1147A GBM 17 1577829 1577829 + Missense_Mutation SNP T T C TCGA-26-5132-01A-01D-1486-08 TCGA-26-5132-10A-01D-1486-08 g.chr17:1577829T>C c.3206A>G c.(3205-3207)aAt>aGt p.N1069S GBMLGG 17 1557307 1557307 + Silent SNP C C T TCGA-FN-7833-01A-11D-2086-08 TCGA-FN-7833-10A-01D-2086-08 g.chr17:1557307C>T c.5991G>A c.(5989-5991)gtG>gtA p.V1997V GBMLGG 17 1558720 1558720 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:1558720G>T c.5911C>A c.(5911-5913)Ctg>Atg p.L1971M GBMLGG 17 1561966 1561966 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:1561966G>A c.5230C>T c.(5230-5232)Cgt>Tgt p.R1744C GBMLGG 17 1576707 1576707 + Missense_Mutation SNP G G A TCGA-DU-A76L-01A-11D-A32B-08 TCGA-DU-A76L-10A-01D-A329-08 g.chr17:1576707G>A c.3601C>T c.(3601-3603)Cgc>Tgc p.R1201C GBMLGG 17 1577046 1577046 + Missense_Mutation SNP A A G TCGA-14-0790-01B-01D-1494-08 TCGA-14-0790-10A-01D-1494-08 g.chr17:1577046A>G c.3440T>C c.(3439-3441)gTt>gCt p.V1147A GBMLGG 17 1577065 1577065 + Missense_Mutation SNP G G A TCGA-CS-4938-01B-11D-1893-08 TCGA-CS-4938-10A-01D-1893-08 g.chr17:1577065G>A c.3421C>T c.(3421-3423)Cgc>Tgc p.R1141C GBMLGG 17 1577829 1577829 + Missense_Mutation SNP T T C TCGA-26-5132-01A-01D-1486-08 TCGA-26-5132-10A-01D-1486-08 g.chr17:1577829T>C c.3206A>G c.(3205-3207)aAt>aGt p.N1069S GBMLGG 17 1578465 1578465 + Missense_Mutation SNP T T C TCGA-DB-A64L-01A-11D-A29Q-08 TCGA-DB-A64L-10A-01D-A29Q-08 g.chr17:1578465T>C c.3041A>G c.(3040-3042)aAc>aGc p.N1014S GBMLGG 17 1578513 1578513 + Missense_Mutation SNP C C T TCGA-WH-A86K-01A-11D-A36O-08 TCGA-WH-A86K-10A-01D-A367-08 g.chr17:1578513C>T c.2993G>A c.(2992-2994)cGc>cAc p.R998H GBMLGG 17 1578972 1578972 + Silent SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:1578972G>T c.2814C>A c.(2812-2814)ccC>ccA p.P938P GBMLGG 17 1578988 1578988 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:1578988C>T c.2798G>A c.(2797-2799)cGc>cAc p.R933H GBMLGG 17 1579960 1579960 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:1579960C>T c.2227G>A c.(2227-2229)Gtg>Atg p.V743M GBMLGG 17 1582120 1582120 + Missense_Mutation SNP C C T TCGA-FG-A87N-01A-11D-A36O-08 TCGA-FG-A87N-10A-01D-A367-08 g.chr17:1582120C>T c.1655G>A c.(1654-1656)cGt>cAt p.R552H GBMLGG 17 1584919 1584919 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:1584919C>T c.719G>A c.(718-720)cGc>cAc p.R240H GBMLGG 17 1585131 1585131 + Silent SNP C C T TCGA-DU-7290-01A-11D-2024-08 TCGA-DU-7290-10A-01D-2024-08 g.chr17:1585131C>T c.636G>A c.(634-636)ccG>ccA p.P212P HNSC 17 1554577 1554577 + Silent SNP C C A TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr17:1554577C>A c.6678G>T c.(6676-6678)acG>acT p.T2226T HNSC 17 1555043 1555043 + Missense_Mutation SNP G G C TCGA-CQ-7072-01A-21D-A30E-08 TCGA-CQ-7072-10A-01D-A30H-08 g.chr17:1555043G>C c.6409C>G c.(6409-6411)Ccc>Gcc p.P2137A HNSC 17 1561562 1561562 + Silent SNP C C T TCGA-CN-A63Y-01A-11D-A30E-08 TCGA-CN-A63Y-10A-01D-A30H-08 g.chr17:1561562C>T c.5490G>A c.(5488-5490)caG>caA p.Q1830Q HNSC 17 1562841 1562841 + Splice_Site SNP C C A TCGA-CV-6955-01A-11D-2012-08 TCGA-CV-6955-10A-01D-2013-08 g.chr17:1562841C>A c.4948G>T c.(4948-4950)Gat>Tat p.D1650Y HNSC 17 1563822 1563822 + Silent SNP G G A TCGA-BA-A6DG-01A-21D-A30E-08 TCGA-BA-A6DG-10A-01D-A30H-08 g.chr17:1563822G>A c.4689C>T c.(4687-4689)caC>caT p.H1563H HNSC 17 1576801 1576801 + Missense_Mutation SNP C C A TCGA-BA-6869-01A-11D-1870-08 TCGA-BA-6869-10A-01D-1870-08 g.chr17:1576801C>A c.3507G>T c.(3505-3507)caG>caT p.Q1169H HNSC 17 1578550 1578550 + Missense_Mutation SNP C C G TCGA-HD-A633-01A-11D-A28R-08 TCGA-HD-A633-10A-01D-A28U-08 g.chr17:1578550C>G c.2956G>C c.(2956-2958)Gag>Cag p.E986Q HNSC 17 1579861 1579861 + Missense_Mutation SNP G G T TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr17:1579861G>T c.2326C>A c.(2326-2328)Ctg>Atg p.L776M HNSC 17 1580919 1580919 + Missense_Mutation SNP G G A TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr17:1580919G>A c.1924C>T c.(1924-1926)Cgt>Tgt p.R642C HNSC 17 1582167 1582167 + Missense_Mutation SNP C C G TCGA-CV-7099-01A-41D-2012-08 TCGA-CV-7099-10A-01D-2013-08 g.chr17:1582167C>G c.1608G>C c.(1606-1608)aaG>aaC p.K536N HNSC 17 1582344 1582344 + Silent SNP G G A TCGA-CV-A45Y-01A-11D-A25D-08 TCGA-CV-A45Y-10A-01D-A25E-08 g.chr17:1582344G>A c.1566C>T c.(1564-1566)ttC>ttT p.F522F HNSC 17 1582626 1582626 + Silent SNP C C G TCGA-CV-7099-01A-41D-2012-08 TCGA-CV-7099-10A-01D-2013-08 g.chr17:1582626C>G c.1368G>C c.(1366-1368)ctG>ctC p.L456L HNSC 17 1582626 1582626 + Silent SNP C C T TCGA-CR-6480-01A-11D-1870-08 TCGA-CR-6480-10A-01D-1870-08 g.chr17:1582626C>T c.1368G>A c.(1366-1368)ctG>ctA p.L456L HNSC 17 1584266 1584266 + Missense_Mutation SNP G G A TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr17:1584266G>A c.949C>T c.(949-951)Cct>Tct p.P317S HNSC 17 1584903 1584903 + Silent SNP G G A TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr17:1584903G>A c.735C>T c.(733-735)ctC>ctT p.L245L HNSC 17 1585124 1585124 + Missense_Mutation SNP C C G TCGA-KU-A66S-01A-21D-A30E-08 TCGA-KU-A66S-10A-01D-A30H-08 g.chr17:1585124C>G c.643G>C c.(643-645)Gac>Cac p.D215H HNSC 17 1585429 1585429 + Missense_Mutation SNP T T G TCGA-CQ-7072-01A-21D-A30E-08 TCGA-CQ-7072-10A-01D-A30H-08 g.chr17:1585429T>G c.428A>C c.(427-429)cAg>cCg p.Q143P HNSC 17 1586884 1586884 + Missense_Mutation SNP C C T TCGA-CN-4723-01A-01D-1434-08 TCGA-CN-4723-10A-01D-1434-08 g.chr17:1586884C>T c.212G>A c.(211-213)cGa>cAa p.R71Q HNSC 17 1586992 1586992 + Missense_Mutation SNP C C G TCGA-P3-A6T4-01A-11D-A34J-08 TCGA-P3-A6T4-10A-01D-A34M-08 g.chr17:1586992C>G c.104G>C c.(103-105)cGa>cCa p.R35P KIPAN 17 1557299 1557299 + Missense_Mutation SNP G G A TCGA-B0-5098-01A-01D-1421-08 TCGA-B0-5098-11A-01D-1421-08 g.chr17:1557299G>A c.5999C>T c.(5998-6000)gCa>gTa p.A2000V KIPAN 17 1559850 1559855 + In_Frame_Del DEL GTAAGT GTAAGT - TCGA-CW-6090-01A-11D-1669-08 TCGA-CW-6090-11A-01D-1669-08 g.chr17:1559850_1559855delGTAAGT c.5624_5629delACTTAC c.(5623-5631)cacttactg>ctg p.HL1875del KIPAN 17 1564002 1564002 + Missense_Mutation SNP T T A TCGA-B0-4811-01A-01D-1501-10 TCGA-B0-4811-11A-02D-1501-10 g.chr17:1564002T>A c.4628A>T c.(4627-4629)aAt>aTt p.N1543I KIPAN 17 1564455 1564455 + Splice_Site SNP A A T TCGA-BQ-5889-01A-11D-1589-08 TCGA-BQ-5889-11A-01D-1589-08 g.chr17:1564455A>T c.4340T>A c.(4339-4341)gTt>gAt p.V1447D KIPAN 17 1564944 1564944 + Missense_Mutation SNP T T G TCGA-2Z-A9JL-01A-11D-A42J-10 TCGA-2Z-A9JL-10A-01D-A42M-10 g.chr17:1564944T>G c.4163A>C c.(4162-4164)gAg>gCg p.E1388A KIPAN 17 1577101 1577101 + Missense_Mutation SNP T T A TCGA-B4-5836-01A-11D-1669-08 TCGA-B4-5836-10A-01D-1669-08 g.chr17:1577101T>A c.3385A>T c.(3385-3387)Aat>Tat p.N1129Y KIPAN 17 1579248 1579248 + Missense_Mutation SNP G G A TCGA-CJ-4923-01A-01D-1429-08 TCGA-CJ-4923-11A-01D-1429-08 g.chr17:1579248G>A c.2653C>T c.(2653-2655)Ctc>Ttc p.L885F KIPAN 17 1582621 1582621 + Missense_Mutation SNP G G A TCGA-B0-5119-01A-02D-1421-08 TCGA-B0-5119-11A-01D-1421-08 g.chr17:1582621G>A c.1373C>T c.(1372-1374)gCc>gTc p.A458V KIPAN 17 1584776 1584776 + Missense_Mutation SNP G G C TCGA-B0-4837-01A-01D-1373-10 TCGA-B0-4837-11A-01D-1373-10 g.chr17:1584776G>C c.862C>G c.(862-864)Cta>Gta p.L288V KIPAN 17 1585300 1585301 + Frame_Shift_Ins INS - - T TCGA-HE-A5NI-01A-11D-A26P-10 TCGA-HE-A5NI-10A-01D-A26P-10 g.chr17:1585300_1585301insT c.466_467insA c.(466-468)agafs p.R156fs KIPAN 17 1586885 1586885 + Missense_Mutation SNP G G C TCGA-HE-7130-01A-11D-1961-08 TCGA-HE-7130-10A-01D-1962-08 g.chr17:1586885G>C c.211C>G c.(211-213)Cga>Gga p.R71G KIPAN 17 1586888 1586888 + Missense_Mutation SNP T T G TCGA-BP-5004-01A-01D-1462-08 TCGA-BP-5004-11A-01D-1462-08 g.chr17:1586888T>G c.208A>C c.(208-210)Att>Ctt p.I70L KIRC 17 1557299 1557299 + Missense_Mutation SNP G G A TCGA-B0-5098-01A-01D-1421-08 TCGA-B0-5098-11A-01D-1421-08 g.chr17:1557299G>A c.5999C>T c.(5998-6000)gCa>gTa p.A2000V KIRC 17 1559850 1559855 + In_Frame_Del DEL GTAAGT GTAAGT - TCGA-CW-6090-01A-11D-1669-08 TCGA-CW-6090-11A-01D-1669-08 g.chr17:1559850_1559855delGTAAGT c.5624_5629delACTTAC c.(5623-5631)cacttactg>ctg p.HL1875del KIRC 17 1564002 1564002 + Missense_Mutation SNP T T A TCGA-B0-4811-01A-01D-1501-10 TCGA-B0-4811-11A-02D-1501-10 g.chr17:1564002T>A c.4628A>T c.(4627-4629)aAt>aTt p.N1543I KIRC 17 1577101 1577101 + Missense_Mutation SNP T T A TCGA-B4-5836-01A-11D-1669-08 TCGA-B4-5836-10A-01D-1669-08 g.chr17:1577101T>A c.3385A>T c.(3385-3387)Aat>Tat p.N1129Y KIRC 17 1579248 1579248 + Missense_Mutation SNP G G A TCGA-CJ-4923-01A-01D-1429-08 TCGA-CJ-4923-11A-01D-1429-08 g.chr17:1579248G>A c.2653C>T c.(2653-2655)Ctc>Ttc p.L885F KIRC 17 1582621 1582621 + Missense_Mutation SNP G G A TCGA-B0-5119-01A-02D-1421-08 TCGA-B0-5119-11A-01D-1421-08 g.chr17:1582621G>A c.1373C>T c.(1372-1374)gCc>gTc p.A458V KIRC 17 1584776 1584776 + Missense_Mutation SNP G G C TCGA-B0-4837-01A-01D-1373-10 TCGA-B0-4837-11A-01D-1373-10 g.chr17:1584776G>C c.862C>G c.(862-864)Cta>Gta p.L288V KIRC 17 1586888 1586888 + Missense_Mutation SNP T T G TCGA-BP-5004-01A-01D-1462-08 TCGA-BP-5004-11A-01D-1462-08 g.chr17:1586888T>G c.208A>C c.(208-210)Att>Ctt p.I70L KIRP 17 1564455 1564455 + Splice_Site SNP A A T TCGA-BQ-5889-01A-11D-1589-08 TCGA-BQ-5889-11A-01D-1589-08 g.chr17:1564455A>T c.4340T>A c.(4339-4341)gTt>gAt p.V1447D KIRP 17 1564944 1564944 + Missense_Mutation SNP T T G TCGA-2Z-A9JL-01A-11D-A42J-10 TCGA-2Z-A9JL-10A-01D-A42M-10 g.chr17:1564944T>G c.4163A>C c.(4162-4164)gAg>gCg p.E1388A KIRP 17 1585300 1585301 + Frame_Shift_Ins INS - - T TCGA-HE-A5NI-01A-11D-A26P-10 TCGA-HE-A5NI-10A-01D-A26P-10 g.chr17:1585300_1585301insT c.466_467insA c.(466-468)agafs p.R156fs KIRP 17 1586885 1586885 + Missense_Mutation SNP G G C TCGA-HE-7130-01A-11D-1961-08 TCGA-HE-7130-10A-01D-1962-08 g.chr17:1586885G>C c.211C>G c.(211-213)Cga>Gga p.R71G LAML 17 1561947 1561947 + Missense_Mutation SNP C C T TCGA-AB-3001-03A-01D-0739-09 TCGA-AB-3001-11A-01D-0739-09 g.chr17:1561947C>T c.5249G>A c.(5248-5250)gGg>gAg p.G1750E LAML 17 1580392 1580392 + Missense_Mutation SNP C C G TCGA-AB-2904-03A-01W-0732-08 TCGA-AB-2904-11A-01W-0732-08 g.chr17:1580392C>G c.2059G>C c.(2059-2061)Gca>Cca p.A687P LGG 17 1557307 1557307 + Silent SNP C C T TCGA-FN-7833-01A-11D-2086-08 TCGA-FN-7833-10A-01D-2086-08 g.chr17:1557307C>T c.5991G>A c.(5989-5991)gtG>gtA p.V1997V LGG 17 1558720 1558720 + Missense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:1558720G>T c.5911C>A c.(5911-5913)Ctg>Atg p.L1971M LGG 17 1561966 1561966 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:1561966G>A c.5230C>T c.(5230-5232)Cgt>Tgt p.R1744C LGG 17 1576707 1576707 + Missense_Mutation SNP G G A TCGA-DU-A76L-01A-11D-A32B-08 TCGA-DU-A76L-10A-01D-A329-08 g.chr17:1576707G>A c.3601C>T c.(3601-3603)Cgc>Tgc p.R1201C LGG 17 1577065 1577065 + Missense_Mutation SNP G G A TCGA-CS-4938-01B-11D-1893-08 TCGA-CS-4938-10A-01D-1893-08 g.chr17:1577065G>A c.3421C>T c.(3421-3423)Cgc>Tgc p.R1141C LGG 17 1578465 1578465 + Missense_Mutation SNP T T C TCGA-DB-A64L-01A-11D-A29Q-08 TCGA-DB-A64L-10A-01D-A29Q-08 g.chr17:1578465T>C c.3041A>G c.(3040-3042)aAc>aGc p.N1014S LGG 17 1578513 1578513 + Missense_Mutation SNP C C T TCGA-WH-A86K-01A-11D-A36O-08 TCGA-WH-A86K-10A-01D-A367-08 g.chr17:1578513C>T c.2993G>A c.(2992-2994)cGc>cAc p.R998H LGG 17 1578972 1578972 + Silent SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:1578972G>T c.2814C>A c.(2812-2814)ccC>ccA p.P938P LGG 17 1578988 1578988 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:1578988C>T c.2798G>A c.(2797-2799)cGc>cAc p.R933H LGG 17 1579960 1579960 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:1579960C>T c.2227G>A c.(2227-2229)Gtg>Atg p.V743M LGG 17 1582120 1582120 + Missense_Mutation SNP C C T TCGA-FG-A87N-01A-11D-A36O-08 TCGA-FG-A87N-10A-01D-A367-08 g.chr17:1582120C>T c.1655G>A c.(1654-1656)cGt>cAt p.R552H LGG 17 1584919 1584919 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr17:1584919C>T c.719G>A c.(718-720)cGc>cAc p.R240H LGG 17 1585131 1585131 + Silent SNP C C T TCGA-DU-7290-01A-11D-2024-08 TCGA-DU-7290-10A-01D-2024-08 g.chr17:1585131C>T c.636G>A c.(634-636)ccG>ccA p.P212P LIHC 17 1554097 1554097 + Silent SNP C C T TCGA-XR-A8TG-01A-11D-A35Z-10 TCGA-XR-A8TG-10A-01D-A35Z-10 g.chr17:1554097C>T c.7007G>A c.(7006-7008)tGa>tAa p.*2336* LIHC 17 1554134 1554134 + Frame_Shift_Del DEL C C - TCGA-G3-A3CJ-01A-11D-A20W-10 TCGA-G3-A3CJ-10A-01D-A20W-10 g.chr17:1554134delC c.6970delG c.(6970-6972)gagfs p.E2324fs LIHC 17 1554786 1554786 + Missense_Mutation SNP T T C TCGA-K7-A5RF-01A-11D-A28X-10 TCGA-K7-A5RF-10B-01D-A28X-10 g.chr17:1554786T>C c.6572A>G c.(6571-6573)cAg>cGg p.Q2191R LIHC 17 1564062 1564062 + Missense_Mutation SNP C C A TCGA-DD-A1E9-01A-21D-A152-10 TCGA-DD-A1E9-11A-11D-A152-10 g.chr17:1564062C>A c.4568G>T c.(4567-4569)cGa>cTa p.R1523L LIHC 17 1577803 1577803 + Missense_Mutation SNP C C T TCGA-ZP-A9D0-01A-11D-A36X-10 TCGA-ZP-A9D0-10A-01D-A370-10 g.chr17:1577803C>T c.3232G>A c.(3232-3234)Gcc>Acc p.A1078T LIHC 17 1580416 1580416 + Missense_Mutation SNP A A T TCGA-FV-A3R2-01A-11D-A22F-10 TCGA-FV-A3R2-11A-11D-A22F-10 g.chr17:1580416A>T c.2035T>A c.(2035-2037)Tca>Aca p.S679T LIHC 17 1582362 1582362 + Silent SNP C C A TCGA-DD-AADJ-01A-11D-A40R-10 TCGA-DD-AADJ-10A-01D-A40U-10 g.chr17:1582362C>A c.1548G>T c.(1546-1548)ctG>ctT p.L516L LIHC 17 1584082 1584082 + Missense_Mutation SNP C C A TCGA-5R-AA1C-01A-11D-A40R-10 TCGA-5R-AA1C-10A-01D-A40U-10 g.chr17:1584082C>A c.1036G>T c.(1036-1038)Gac>Tac p.D346Y LIHC 17 1584925 1584925 + Missense_Mutation SNP A A C TCGA-2Y-A9GW-01A-11D-A382-10 TCGA-2Y-A9GW-10A-01D-A385-10 g.chr17:1584925A>C c.713T>G c.(712-714)cTc>cGc p.L238R LIHC 17 1585147 1585147 + Missense_Mutation SNP A A G TCGA-CC-A3MB-01A-11D-A20W-10 TCGA-CC-A3MB-10A-01D-A20W-10 g.chr17:1585147A>G c.620T>C c.(619-621)tTc>tCc p.F207S LUAD 17 1554421 1554421 + Silent SNP C C A TCGA-55-7281-01A-11D-2036-08 TCGA-55-7281-10A-01D-2036-08 g.chr17:1554421C>A c.6834G>T c.(6832-6834)tcG>tcT p.S2278S LUAD 17 1557163 1557163 + Silent SNP G G A TCGA-05-4432-01A-01D-1265-08 TCGA-05-4432-10A-01D-1265-08 g.chr17:1557163G>A c.6135C>T c.(6133-6135)cgC>cgT p.R2045R LUAD 17 1558656 1558656 + Missense_Mutation SNP C C A TCGA-55-A490-01A-11D-A24D-08 TCGA-55-A490-10A-01D-A24F-08 g.chr17:1558656C>A c.5975G>T c.(5974-5976)gGc>gTc p.G1992V LUAD 17 1558657 1558657 + Missense_Mutation SNP C C A TCGA-55-A490-01A-11D-A24D-08 TCGA-55-A490-10A-01D-A24F-08 g.chr17:1558657C>A c.5974G>T c.(5974-5976)Ggc>Tgc p.G1992C LUAD 17 1560029 1560029 + Missense_Mutation SNP C C A TCGA-86-8359-01A-11D-2323-08 TCGA-86-8359-10A-01D-2323-08 g.chr17:1560029C>A c.5532G>T c.(5530-5532)gaG>gaT p.E1844D LUAD 17 1563743 1563743 + Missense_Mutation SNP C C G TCGA-62-8399-01A-21D-2323-08 TCGA-62-8399-10A-01D-2323-08 g.chr17:1563743C>G c.4768G>C c.(4768-4770)Gtt>Ctt p.V1590L LUAD 17 1563786 1563786 + Missense_Mutation SNP C C A TCGA-05-4397-01A-01D-1265-08 TCGA-05-4397-10A-01D-1265-08 g.chr17:1563786C>A c.4725G>T c.(4723-4725)caG>caT p.Q1575H LUAD 17 1563823 1563823 + Missense_Mutation SNP T T C TCGA-86-8279-01A-11D-2284-08 TCGA-86-8279-10A-01D-2284-08 g.chr17:1563823T>C c.4688A>G c.(4687-4689)cAc>cGc p.H1563R LUAD 17 1576725 1576725 + Missense_Mutation SNP G G A TCGA-97-A4M3-01A-11D-A24P-08 TCGA-97-A4M3-10A-01D-A24P-08 g.chr17:1576725G>A c.3583C>T c.(3583-3585)Cgc>Tgc p.R1195C LUAD 17 1577912 1577912 + Silent SNP C C T TCGA-55-7995-01A-11D-2184-08 TCGA-55-7995-10A-01D-2184-08 g.chr17:1577912C>T c.3123G>A c.(3121-3123)gtG>gtA p.V1041V LUAD 17 1578503 1578503 + Silent SNP C C A TCGA-05-4410-01A-21D-1855-08 TCGA-05-4410-10A-01D-1855-08 g.chr17:1578503C>A c.3003G>T c.(3001-3003)gtG>gtT p.V1001V LUAD 17 1579293 1579293 + Missense_Mutation SNP C C A TCGA-38-4626-01A-01D-1553-08 TCGA-38-4626-11A-01D-1553-08 g.chr17:1579293C>A c.2608G>T c.(2608-2610)Gcc>Tcc p.A870S LUAD 17 1579338 1579338 + Missense_Mutation SNP G G A TCGA-55-8204-01A-11D-2238-08 TCGA-55-8204-10A-01D-2238-08 g.chr17:1579338G>A c.2563C>T c.(2563-2565)Cgg>Tgg p.R855W LUAD 17 1583007 1583007 + Silent SNP T T A TCGA-17-Z055-01A-01W-0747-08 TCGA-17-Z055-11A-01W-0747-08 g.chr17:1583007T>A c.1185A>T c.(1183-1185)acA>acT p.T395T LUAD 17 1584926 1584926 + Missense_Mutation SNP G G A TCGA-17-Z056-01A-01W-0747-08 TCGA-17-Z056-11A-01W-0747-08 g.chr17:1584926G>A c.712C>T c.(712-714)Ctc>Ttc p.L238F LUSC 17 1554484 1554484 + Missense_Mutation SNP C C G TCGA-66-2785-01A-01D-1522-08 TCGA-66-2785-11A-01D-1522-08 g.chr17:1554484C>G c.6771G>C c.(6769-6771)gaG>gaC p.E2257D LUSC 17 1577070 1577070 + Missense_Mutation SNP C C A TCGA-22-5472-01A-01D-1632-08 TCGA-22-5472-11A-11D-1632-08 g.chr17:1577070C>A c.3416G>T c.(3415-3417)cGc>cTc p.R1139L LUSC 17 1582317 1582317 + Silent SNP G G A TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr17:1582317G>A c.1593C>T c.(1591-1593)acC>acT p.T531T LUSC 17 1582619 1582619 + Missense_Mutation SNP G G C TCGA-22-5477-01A-01D-1632-08 TCGA-22-5477-11A-11D-1632-08 g.chr17:1582619G>C c.1375C>G c.(1375-1377)Ctg>Gtg p.L459V LUSC 17 1582704 1582704 + Splice_Site SNP C C G TCGA-85-6561-01A-11D-1817-08 TCGA-85-6561-10A-01D-1817-08 g.chr17:1582704C>G c.1290G>C c.(1288-1290)tgG>tgC p.W430C LUSC 17 1584337 1584337 + Missense_Mutation SNP C C A TCGA-85-6561-01A-11D-1817-08 TCGA-85-6561-10A-01D-1817-08 g.chr17:1584337C>A c.878G>T c.(877-879)tGg>tTg p.W293L LUSC 17 1585180 1585180 + Missense_Mutation SNP T T A TCGA-34-5927-01A-11D-1817-08 TCGA-34-5927-10A-01D-1817-08 g.chr17:1585180T>A c.587A>T c.(586-588)gAc>gTc p.D196V LUSC 17 1585256 1585256 + Missense_Mutation SNP C C A TCGA-22-1012-01A-01D-1521-08 TCGA-22-1012-11A-01D-1521-08 g.chr17:1585256C>A c.511G>T c.(511-513)Gat>Tat p.D171Y OV 17 1563792 1563792 + Silent SNP G G A TCGA-61-1728-01A-01W-0699-08 TCGA-61-1728-11A-01W-0700-08 g.chr17:1563792G>A c.4719C>T c.(4717-4719)ctC>ctT p.L1573L OV 17 1578513 1578513 + Missense_Mutation SNP C C G TCGA-24-1469-01A-01W-0553-09 TCGA-24-1469-10A-01W-0553-09 g.chr17:1578513C>G c.2993G>C c.(2992-2994)cGc>cCc p.R998P PAAD 17 1556843 1556843 + Missense_Mutation SNP C C T TCGA-3A-A9IO-01A-11D-A38G-08 TCGA-3A-A9IO-10A-01D-A38J-08 g.chr17:1556843C>T c.6362G>A c.(6361-6363)cGg>cAg p.R2121Q PAAD 17 1563232 1563232 + Nonsense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr17:1563232G>A c.4849C>T c.(4849-4851)Cga>Tga p.R1617* PAAD 17 1563731 1563731 + Missense_Mutation SNP A A G TCGA-3A-A9IJ-01A-11D-A397-08 TCGA-3A-A9IJ-10A-01D-A39A-08 g.chr17:1563731A>G c.4780T>C c.(4780-4782)Tgt>Cgt p.C1594R PAAD 17 1563837 1563837 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr17:1563837C>T c.4674G>A c.(4672-4674)acG>acA p.T1558T PAAD 17 1576444 1576444 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr17:1576444C>T c.3705G>A c.(3703-3705)gaG>gaA p.E1235E PAAD 17 1576724 1576724 + Missense_Mutation SNP C C T TCGA-HV-A7OL-01A-11D-A33T-08 TCGA-HV-A7OL-10A-01D-A33W-08 g.chr17:1576724C>T c.3584G>A c.(3583-3585)cGc>cAc p.R1195H PAAD 17 1577065 1577065 + Missense_Mutation SNP G G A TCGA-HZ-A77P-01A-11D-A33T-08 TCGA-HZ-A77P-10A-01D-A33W-08 g.chr17:1577065G>A c.3421C>T c.(3421-3423)Cgc>Tgc p.R1141C PAAD 17 1577065 1577065 + Missense_Mutation SNP G G A TCGA-HZ-A8P1-01A-11D-A377-08 TCGA-HZ-A8P1-10A-01D-A37A-08 g.chr17:1577065G>A c.3421C>T c.(3421-3423)Cgc>Tgc p.R1141C PAAD 17 1577073 1577073 + Missense_Mutation SNP G G A TCGA-HZ-A77O-01A-11D-A33T-08 TCGA-HZ-A77O-10A-01D-A33W-08 g.chr17:1577073G>A c.3413C>T c.(3412-3414)gCc>gTc p.A1138V PAAD 17 1585273 1585273 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr17:1585273C>T c.494G>A c.(493-495)cGt>cAt p.R165H PAAD 17 1585571 1585571 + Missense_Mutation SNP G G A TCGA-RB-A7B8-01A-12D-A33T-08 TCGA-RB-A7B8-10A-01D-A33W-08 g.chr17:1585571G>A c.286C>T c.(286-288)Ccc>Tcc p.P96S PCPG 17 1554459 1554459 + Missense_Mutation SNP G G A TCGA-QR-A6GY-01A-11D-A35D-08 TCGA-QR-A6GY-10A-01D-A35B-08 g.chr17:1554459G>A c.6796C>T c.(6796-6798)Cgt>Tgt p.R2266C PCPG 17 1577856 1577856 + Missense_Mutation SNP T T C TCGA-WB-A819-01A-11D-A35I-08 TCGA-WB-A819-10A-01D-A35G-08 g.chr17:1577856T>C c.3179A>G c.(3178-3180)gAg>gGg p.E1060G PRAD 17 1559946 1559946 + Missense_Mutation SNP A A C TCGA-CH-5750-01A-11D-1576-08 TCGA-CH-5750-10A-01D-1576-08 g.chr17:1559946A>C c.5615T>G c.(5614-5616)cTg>cGg p.L1872R PRAD 17 1560049 1560049 + Missense_Mutation SNP T T C TCGA-EJ-A65D-01A-11D-A30E-08 TCGA-EJ-A65D-10A-01D-A30H-08 g.chr17:1560049T>C c.5512A>G c.(5512-5514)Aag>Gag p.K1838E PRAD 17 1563231 1563231 + Missense_Mutation SNP C C T TCGA-KK-A7AY-01A-11D-A33T-08 TCGA-KK-A7AY-11A-21D-A33W-08 g.chr17:1563231C>T c.4850G>A c.(4849-4851)cGa>cAa p.R1617Q PRAD 17 1563822 1563822 + Silent SNP G G A TCGA-EJ-7321-01A-31D-2260-08 TCGA-EJ-7321-10A-01D-2260-08 g.chr17:1563822G>A c.4689C>T c.(4687-4689)caC>caT p.H1563H PRAD 17 1577185 1577216 + Splice_Site DEL ACCTACACCAGACCAGGTACACTGCTGAGGCC ACCTACACCAGACCAGGTACACTGCTGAGGCC - TCGA-YL-A9WL-01A-11D-A41K-08 TCGA-YL-A9WL-10A-01D-A41N-08 g.chr17:1577185_1577216delACCTACACCAGACCAGGTACACTGCTGAGGCC c.3300_3301delGGCCTCAGCAGTGTACCTGGTCTGGTGTAGGT c.(3298-3303)agggcc>agcc p.RA1100fs PRAD 17 1577960 1577960 + Silent SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr17:1577960C>T c.3075G>A c.(3073-3075)acG>acA p.T1025T PRAD 17 1584933 1584933 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr17:1584933C>T c.705G>A c.(703-705)atG>atA p.M235I PRAD 17 1585167 1585167 + Silent SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr17:1585167G>A c.600C>T c.(598-600)gaC>gaT p.D200D READ 17 1579255 1579255 + Silent SNP C C T TCGA-AG-3594-01A-02W-0831-10 TCGA-AG-3594-10A-01W-0831-10 g.chr17:1579255C>T c.2646G>A c.(2644-2646)aaG>aaA p.K882K READ 17 1584923 1584924 + Frame_Shift_Del DEL AG AG - TCGA-AG-A02N-01A-11W-A096-10 TCGA-AG-A02N-11A-11W-A096-10 g.chr17:1584923_1584924delAG c.714_715delCT c.(712-717)ctctacfs p.Y239fs READ 17 1585217 1585217 + Missense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr17:1585217C>A c.550G>T c.(550-552)Gat>Tat p.D184Y SARC 17 1557276 1557276 + Nonsense_Mutation SNP G G A TCGA-QC-A7B5-01A-11D-A33E-09 TCGA-QC-A7B5-11A-11D-A33H-09 g.chr17:1557276G>A c.6022C>T c.(6022-6024)Cga>Tga p.R2008* SARC 17 1559969 1559969 + Silent SNP G G T TCGA-IF-A4AK-01A-21D-A24N-09 TCGA-IF-A4AK-11A-11D-A24N-09 g.chr17:1559969G>T c.5592C>A c.(5590-5592)acC>acA p.T1864T SARC 17 1577107 1577107 + Missense_Mutation SNP C C T TCGA-DX-AB2O-01A-12D-A38Z-09 TCGA-DX-AB2O-10A-01D-A38Z-09 g.chr17:1577107C>T c.3379G>A c.(3379-3381)Ggc>Agc p.G1127S SARC 17 1584027 1584027 + Missense_Mutation SNP G G A TCGA-DX-AB2O-01A-12D-A38Z-09 TCGA-DX-AB2O-10A-01D-A38Z-09 g.chr17:1584027G>A c.1091C>T c.(1090-1092)tCa>tTa p.S364L SARC 17 1584068 1584068 + Missense_Mutation SNP G G C TCGA-DX-AB2O-01A-12D-A38Z-09 TCGA-DX-AB2O-10A-01D-A38Z-09 g.chr17:1584068G>C c.1050C>G c.(1048-1050)ttC>ttG p.F350L SKCM 17 1555054 1555054 + Missense_Mutation SNP G G A TCGA-EE-A2GI-06A-11D-A196-08 TCGA-EE-A2GI-10A-01D-A198-08 g.chr17:1555054G>A c.6398C>T c.(6397-6399)cCa>cTa p.P2133L SKCM 17 1558786 1558786 + Missense_Mutation SNP G G A TCGA-EE-A2GU-06A-11D-A196-08 TCGA-EE-A2GU-10A-01D-A198-08 g.chr17:1558786G>A c.5845C>T c.(5845-5847)Cgg>Tgg p.R1949W SKCM 17 1558805 1558805 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr17:1558805G>A c.5826C>T c.(5824-5826)gcC>gcT p.A1942A SKCM 17 1559773 1559773 + Silent SNP G G A TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr17:1559773G>A c.5706C>T c.(5704-5706)ttC>ttT p.F1902F SKCM 17 1562025 1562025 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr17:1562025G>A c.5171C>T c.(5170-5172)cCt>cTt p.P1724L SKCM 17 1562737 1562737 + Silent SNP G G A TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr17:1562737G>A c.5052C>T c.(5050-5052)ttC>ttT p.F1684F SKCM 17 1563247 1563247 + Missense_Mutation SNP C C T TCGA-EE-A2A2-06A-11D-A196-08 TCGA-EE-A2A2-10A-01D-A198-08 g.chr17:1563247C>T c.4834G>A c.(4834-4836)Gag>Aag p.E1612K SKCM 17 1563755 1563755 + Missense_Mutation SNP G G A TCGA-FS-A1Z7-06A-11D-A197-08 TCGA-FS-A1Z7-10A-01D-A199-08 g.chr17:1563755G>A c.4756C>T c.(4756-4758)Cat>Tat p.H1586Y SKCM 17 1564924 1564924 + Missense_Mutation SNP C C T TCGA-EE-A29A-06A-12D-A196-08 TCGA-EE-A29A-10A-01D-A198-08 g.chr17:1564924C>T c.4183G>A c.(4183-4185)Gag>Aag p.E1395K SKCM 17 1577111 1577111 + Silent SNP G G A TCGA-FS-A1Z3-06A-11D-A197-08 TCGA-FS-A1Z3-10A-01D-A199-08 g.chr17:1577111G>A c.3375C>T c.(3373-3375)atC>atT p.I1125I SKCM 17 1577738 1577738 + Silent SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr17:1577738G>A c.3297C>T c.(3295-3297)ttC>ttT p.F1099F SKCM 17 1577966 1577966 + Silent SNP G G A TCGA-D3-A3C8-06A-12D-A19A-08 TCGA-D3-A3C8-10A-01D-A19A-08 g.chr17:1577966G>A c.3069C>T c.(3067-3069)aaC>aaT p.N1023N SKCM 17 1579044 1579044 + Silent SNP C C A TCGA-EE-A3AG-06A-31D-A196-08 TCGA-EE-A3AG-10A-01D-A198-08 g.chr17:1579044C>A c.2742G>T c.(2740-2742)ctG>ctT p.L914L SKCM 17 1579318 1579318 + Silent SNP C C T TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr17:1579318C>T c.2583G>A c.(2581-2583)agG>agA p.R861R SKCM 17 1580001 1580001 + Missense_Mutation SNP G G A TCGA-ER-A19F-06A-11D-A196-08 TCGA-ER-A19F-10A-01D-A198-08 g.chr17:1580001G>A c.2186C>T c.(2185-2187)cCt>cTt p.P729L SKCM 17 1581861 1581861 + Missense_Mutation SNP A A C TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr17:1581861A>C c.1805T>G c.(1804-1806)aTt>aGt p.I602S SKCM 17 1581892 1581892 + Missense_Mutation SNP A A G TCGA-EE-A3AB-06A-11D-A196-08 TCGA-EE-A3AB-10A-01D-A198-08 g.chr17:1581892A>G c.1774T>C c.(1774-1776)Tat>Cat p.Y592H SKCM 17 1582092 1582092 + Silent SNP G G A TCGA-EE-A2GC-06A-11D-A197-08 TCGA-EE-A2GC-10A-01D-A199-08 g.chr17:1582092G>A c.1683C>T c.(1681-1683)caC>caT p.H561H SKCM 17 1582486 1582486 + Missense_Mutation SNP G G A TCGA-FW-A3TU-06A-11D-A23B-08 TCGA-FW-A3TU-10A-01D-A23B-08 g.chr17:1582486G>A c.1424C>T c.(1423-1425)tCc>tTc p.S475F SKCM 17 1584067 1584067 + Missense_Mutation SNP A A T TCGA-D9-A3Z3-06A-11D-A23B-08 TCGA-D9-A3Z3-10A-01D-A23B-08 g.chr17:1584067A>T c.1051T>A c.(1051-1053)Tac>Aac p.Y351N SKCM 17 1584244 1584244 + Missense_Mutation SNP G G A TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr17:1584244G>A c.971C>T c.(970-972)cCa>cTa p.P324L SKCM 17 1585293 1585293 + Silent SNP C C T TCGA-EE-A3J5-06A-11D-A20D-08 TCGA-EE-A3J5-10A-01D-A20D-08 g.chr17:1585293C>T c.474G>A c.(472-474)agG>agA p.R158R SKCM 17 1585565 1585565 + Missense_Mutation SNP C C T TCGA-GN-A26A-06A-11D-A19A-08 TCGA-GN-A26A-10A-01D-A19A-08 g.chr17:1585565C>T c.292G>A c.(292-294)Gca>Aca p.A98T SKCM 17 1586852 1586852 + Missense_Mutation SNP G G T TCGA-FS-A1ZZ-06A-11D-A197-08 TCGA-FS-A1ZZ-10A-01D-A199-08 g.chr17:1586852G>T c.244C>A c.(244-246)Cgc>Agc p.R82S SKCM 17 1587789 1587789 + Missense_Mutation SNP G G A TCGA-EE-A2A6-06A-11D-A197-08 TCGA-EE-A2A6-10A-01D-A199-08 g.chr17:1587789G>A c.77C>T c.(76-78)tCg>tTg p.S26L

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 17 1554827 1554827 single base substitution C T downstream_gene_variant BLCA-CN 17 1554827 1554827 single base substitution C T exon_variant BLCA-CN 17 1554827 1554827 single base substitution C T stop_gained W2177* 6531G>A BLCA-CN 17 1554827 1554827 single base substitution C T upstream_gene_variant BLCA-CN 17 1558703 1558703 single base substitution C A downstream_gene_variant BLCA-CN 17 1558703 1558703 single base substitution C A missense_variant W1976C 5928G>T BLCA-CN 17 1558703 1558703 single base substitution C A upstream_gene_variant BLCA-CN 17 1558704 1558704 single base substitution C A downstream_gene_variant BLCA-CN 17 1558704 1558704 single base substitution C A missense_variant W1976L 5927G>T BLCA-CN 17 1558704 1558704 single base substitution C A upstream_gene_variant BLCA-CN 17 1559856 1559856 single base substitution G C downstream_gene_variant BLCA-CN 17 1559856 1559856 single base substitution G C missense_variant H1875D 5623C>G BLCA-CN 17 1559856 1559856 single base substitution G C upstream_gene_variant BLCA-CN 17 1580929 1580929 single base substitution G A downstream_gene_variant BLCA-CN 17 1580929 1580929 single base substitution G A synonymous_variant L583L 1749C>T BLCA-CN 17 1580929 1580929 single base substitution G A synonymous_variant L638L 1914C>T BLCA-CN 17 1580929 1580929 single base substitution G A upstream_gene_variant BLCA-US 17 1548932 1548932 single base substitution G A downstream_gene_variant BLCA-US 17 1551226 1551226 single base substitution G A downstream_gene_variant BLCA-US 17 1562039 1562039 single base substitution G A downstream_gene_variant BLCA-US 17 1562039 1562039 single base substitution G A synonymous_variant F1719F 5157C>T BLCA-US 17 1562039 1562039 single base substitution G A upstream_gene_variant BLCA-US 17 1564436 1564436 single base substitution G A exon_variant BLCA-US 17 1564436 1564436 single base substitution G A synonymous_variant F1453F 4359C>T BLCA-US 17 1564436 1564436 single base substitution G A synonymous_variant F96F 288C>T BLCA-US 17 1564447 1564447 single base substitution G C exon_variant BLCA-US 17 1564447 1564447 single base substitution G C missense_variant Q1450E 4348C>G BLCA-US 17 1564447 1564447 single base substitution G C missense_variant Q93E 277C>G BLCA-US 17 1564634 1564634 single base substitution G A exon_variant BLCA-US 17 1564634 1564634 single base substitution G A synonymous_variant F1423F 4269C>T BLCA-US 17 1564634 1564634 single base substitution G A synonymous_variant F66F 198C>T BLCA-US 17 1564634 1564634 single base substitution G A upstream_gene_variant BLCA-US 17 1564962 1564962 single base substitution G C exon_variant BLCA-US 17 1564962 1564962 single base substitution G C intron_variant BLCA-US 17 1564962 1564962 single base substitution G C missense_variant S1382C 4145C>G BLCA-US 17 1564962 1564962 single base substitution G C upstream_gene_variant BLCA-US 17 1576684 1576684 single base substitution G T downstream_gene_variant BLCA-US 17 1576684 1576684 single base substitution G T exon_variant BLCA-US 17 1576684 1576684 single base substitution G T synonymous_variant T1208T 3624C>A BLCA-US 17 1576731 1576731 single base substitution C T downstream_gene_variant BLCA-US 17 1576731 1576731 single base substitution C T missense_variant E1193K 3577G>A BLCA-US 17 1576731 1576731 single base substitution C T upstream_gene_variant BLCA-US 17 1582371 1582371 single base substitution G A downstream_gene_variant BLCA-US 17 1582371 1582371 single base substitution G A exon_variant BLCA-US 17 1582371 1582371 single base substitution G A synonymous_variant L458L 1374C>T BLCA-US 17 1582371 1582371 single base substitution G A synonymous_variant L513L 1539C>T BLCA-US 17 1582371 1582371 single base substitution G A upstream_gene_variant BRCA-EU 17 1550287 1550287 single base substitution A T downstream_gene_variant BRCA-EU 17 1550644 1550644 single base substitution C A downstream_gene_variant BRCA-EU 17 1553187 1553187 single base substitution T C downstream_gene_variant BRCA-EU 17 1553234 1553237 deletion of <=200bp AGGA - downstream_gene_variant BRCA-EU 17 1553323 1553323 single base substitution A G downstream_gene_variant BRCA-EU 17 1553497 1553497 single base substitution C T downstream_gene_variant BRCA-EU 17 1556358 1556358 single base substitution T C exon_variant BRCA-EU 17 1556358 1556358 single base substitution T C intron_variant BRCA-EU 17 1556358 1556358 single base substitution T C upstream_gene_variant BRCA-EU 17 1559046 1559046 single base substitution G C downstream_gene_variant BRCA-EU 17 1559046 1559046 single base substitution G C intron_variant BRCA-EU 17 1559046 1559046 single base substitution G C upstream_gene_variant BRCA-EU 17 1562151 1562151 single base substitution T G downstream_gene_variant BRCA-EU 17 1562151 1562151 single base substitution T G intron_variant BRCA-EU 17 1562151 1562151 single base substitution T G upstream_gene_variant BRCA-EU 17 1562606 1562606 single base substitution C T downstream_gene_variant BRCA-EU 17 1562606 1562606 single base substitution C T intron_variant BRCA-EU 17 1562606 1562606 single base substitution C T upstream_gene_variant BRCA-EU 17 1562850 1562850 single base substitution T C downstream_gene_variant BRCA-EU 17 1562850 1562850 single base substitution T C exon_variant BRCA-EU 17 1562850 1562850 single base substitution T C splice_region_variant BRCA-EU 17 1562850 1562850 single base substitution T C upstream_gene_variant BRCA-EU 17 1563091 1563091 single base substitution C G downstream_gene_variant BRCA-EU 17 1563091 1563091 single base substitution C G exon_variant BRCA-EU 17 1563091 1563091 single base substitution C G intron_variant BRCA-EU 17 1563091 1563091 single base substitution C G upstream_gene_variant BRCA-EU 17 1563492 1563492 single base substitution A G downstream_gene_variant BRCA-EU 17 1563492 1563492 single base substitution A G intron_variant BRCA-EU 17 1564322 1564322 single base substitution C T exon_variant BRCA-EU 17 1564322 1564322 single base substitution C T synonymous_variant K134K 402G>A BRCA-EU 17 1564322 1564322 single base substitution C T synonymous_variant K1491K 4473G>A BRCA-EU 17 1565496 1565496 single base substitution G A intron_variant BRCA-EU 17 1565496 1565496 single base substitution G A upstream_gene_variant BRCA-EU 17 1566691 1566691 single base substitution A G intron_variant BRCA-EU 17 1566691 1566691 single base substitution A G upstream_gene_variant BRCA-EU 17 1567201 1567201 insertion of <=200bp - GATATTTGATATTT intron_variant BRCA-EU 17 1567201 1567201 insertion of <=200bp - GATATTTGATATTT upstream_gene_variant BRCA-EU 17 1567599 1567599 single base substitution T G intron_variant BRCA-EU 17 1567599 1567599 single base substitution T G upstream_gene_variant BRCA-EU 17 1567747 1567747 single base substitution C T intron_variant BRCA-EU 17 1567747 1567747 single base substitution C T upstream_gene_variant BRCA-EU 17 1568296 1568296 deletion of <=200bp A - intron_variant BRCA-EU 17 1568296 1568296 deletion of <=200bp A - upstream_gene_variant BRCA-EU 17 1569127 1569127 single base substitution G A intron_variant BRCA-EU 17 1569127 1569127 single base substitution G A upstream_gene_variant BRCA-EU 17 1570018 1570018 single base substitution C T intron_variant BRCA-EU 17 1570018 1570018 single base substitution C T upstream_gene_variant BRCA-EU 17 1570096 1570096 single base substitution A G intron_variant BRCA-EU 17 1570096 1570096 single base substitution A G upstream_gene_variant BRCA-EU 17 1571947 1571947 single base substitution C T downstream_gene_variant BRCA-EU 17 1571947 1571947 single base substitution C T intron_variant BRCA-EU 17 1573476 1573476 single base substitution G A downstream_gene_variant BRCA-EU 17 1573476 1573476 single base substitution G A intron_variant BRCA-EU 17 1573792 1573792 deletion of <=200bp T - downstream_gene_variant BRCA-EU 17 1573792 1573792 deletion of <=200bp T - intron_variant BRCA-EU 17 1577214 1577214 single base substitution G A downstream_gene_variant BRCA-EU 17 1577214 1577214 single base substitution G A intron_variant BRCA-EU 17 1577214 1577214 single base substitution G A upstream_gene_variant BRCA-EU 17 1578900 1578900 single base substitution C T downstream_gene_variant BRCA-EU 17 1578900 1578900 single base substitution C T intron_variant BRCA-EU 17 1578900 1578900 single base substitution C T upstream_gene_variant BRCA-EU 17 1580724 1580724 single base substitution G C downstream_gene_variant BRCA-EU 17 1580724 1580724 single base substitution G C intron_variant BRCA-EU 17 1580724 1580724 single base substitution G C upstream_gene_variant BRCA-EU 17 1581307 1581307 single base substitution G C downstream_gene_variant BRCA-EU 17 1581307 1581307 single base substitution G C intron_variant BRCA-EU 17 1581307 1581307 single base substitution G C upstream_gene_variant BRCA-EU 17 1581359 1581359 single base substitution A C downstream_gene_variant BRCA-EU 17 1581359 1581359 single base substitution A C intron_variant BRCA-EU 17 1581359 1581359 single base substitution A C upstream_gene_variant BRCA-EU 17 1581678 1581678 single base substitution G A downstream_gene_variant BRCA-EU 17 1581678 1581678 single base substitution G A intron_variant BRCA-EU 17 1581678 1581678 single base substitution G A upstream_gene_variant BRCA-EU 17 1582189 1582189 insertion of <=200bp - A downstream_gene_variant BRCA-EU 17 1582189 1582189 insertion of <=200bp - A intron_variant BRCA-EU 17 1582189 1582189 insertion of <=200bp - A upstream_gene_variant BRCA-EU 17 1582530 1582530 single base substitution A T downstream_gene_variant BRCA-EU 17 1582530 1582530 single base substitution A T intron_variant BRCA-EU 17 1582530 1582530 single base substitution A T upstream_gene_variant BRCA-EU 17 1588426 1588426 single base substitution G A upstream_gene_variant BRCA-EU 17 1588674 1588674 single base substitution G C upstream_gene_variant BRCA-EU 17 1588932 1588932 single base substitution T C upstream_gene_variant BRCA-EU 17 1591214 1591214 single base substitution T G upstream_gene_variant BRCA-EU 17 1591945 1591945 single base substitution C T upstream_gene_variant BRCA-EU 17 1592048 1592048 single base substitution G C upstream_gene_variant BRCA-FR 17 1569696 1569696 single base substitution T A intron_variant BRCA-FR 17 1569696 1569696 single base substitution T A upstream_gene_variant BRCA-FR 17 1571947 1571947 single base substitution C T downstream_gene_variant BRCA-FR 17 1571947 1571947 single base substitution C T intron_variant BRCA-FR 17 1577072 1577072 single base substitution G A downstream_gene_variant BRCA-FR 17 1577072 1577072 single base substitution G A synonymous_variant A1138A 3414C>T BRCA-FR 17 1577072 1577072 single base substitution G A upstream_gene_variant BRCA-FR 17 1577839 1577839 single base substitution G A downstream_gene_variant BRCA-FR 17 1577839 1577839 single base substitution G A stop_gained Q1011* 3031C>T BRCA-FR 17 1577839 1577839 single base substitution G A stop_gained Q1066* 3196C>T BRCA-FR 17 1577839 1577839 single base substitution G A upstream_gene_variant BRCA-FR 17 1592048 1592048 single base substitution G C upstream_gene_variant BRCA-UK 17 1570096 1570096 single base substitution A G intron_variant BRCA-UK 17 1570096 1570096 single base substitution A G upstream_gene_variant BRCA-UK 17 1571118 1571118 single base substitution G A intron_variant BRCA-UK 17 1581818 1581818 single base substitution G A downstream_gene_variant BRCA-UK 17 1581818 1581818 single base substitution G A exon_variant BRCA-UK 17 1581818 1581818 single base substitution G A synonymous_variant F561F 1683C>T BRCA-UK 17 1581818 1581818 single base substitution G A synonymous_variant F616F 1848C>T BRCA-UK 17 1581818 1581818 single base substitution G A upstream_gene_variant BRCA-UK 17 1582530 1582530 single base substitution A T downstream_gene_variant BRCA-UK 17 1582530 1582530 single base substitution A T intron_variant BRCA-UK 17 1582530 1582530 single base substitution A T upstream_gene_variant BRCA-US 17 1554097 1554097 single base substitution C T downstream_gene_variant BRCA-US 17 1554097 1554097 single base substitution C T stop_retained_variant *2336* 7007G>A BRCA-US 17 1554097 1554097 single base substitution C T synonymous_variant L68L 204G>A BRCA-US 17 1554841 1554841 single base substitution C T downstream_gene_variant BRCA-US 17 1554841 1554841 single base substitution C T exon_variant BRCA-US 17 1554841 1554841 single base substitution C T missense_variant E2173K 6517G>A BRCA-US 17 1554841 1554841 single base substitution C T upstream_gene_variant BRCA-US 17 1557290 1557290 single base substitution G A exon_variant BRCA-US 17 1557290 1557290 single base substitution G A missense_variant T2003I 6008C>T BRCA-US 17 1557290 1557290 single base substitution G A upstream_gene_variant BRCA-US 17 1561627 1561627 single base substitution T C downstream_gene_variant BRCA-US 17 1561627 1561627 single base substitution T C missense_variant I1809V 5425A>G BRCA-US 17 1561627 1561627 single base substitution T C upstream_gene_variant BRCA-US 17 1561836 1561836 single base substitution C G downstream_gene_variant BRCA-US 17 1561836 1561836 single base substitution C G missense_variant R1787T 5360G>C BRCA-US 17 1561836 1561836 single base substitution C G upstream_gene_variant BRCA-US 17 1564332 1564332 single base substitution G A exon_variant BRCA-US 17 1564332 1564332 single base substitution G A missense_variant T131I 392C>T BRCA-US 17 1564332 1564332 single base substitution G A missense_variant T1488I 4463C>T BRCA-US 17 1564924 1564924 single base substitution C G exon_variant BRCA-US 17 1564924 1564924 single base substitution C G intron_variant BRCA-US 17 1564924 1564924 single base substitution C G missense_variant E1395Q 4183G>C BRCA-US 17 1564924 1564924 single base substitution C G upstream_gene_variant BRCA-US 17 1576724 1576724 single base substitution C T downstream_gene_variant BRCA-US 17 1576724 1576724 single base substitution C T missense_variant R1195H 3584G>A BRCA-US 17 1576724 1576724 single base substitution C T upstream_gene_variant BRCA-US 17 1577787 1577787 single base substitution T G downstream_gene_variant BRCA-US 17 1577787 1577787 single base substitution T G missense_variant H1083P 3248A>C BRCA-US 17 1577787 1577787 single base substitution T G upstream_gene_variant BRCA-US 17 1578489 1578489 single base substitution G A downstream_gene_variant BRCA-US 17 1578489 1578489 single base substitution G A exon_variant BRCA-US 17 1578489 1578489 single base substitution G A missense_variant A1006V 3017C>T BRCA-US 17 1578489 1578489 single base substitution G A missense_variant A951V 2852C>T BRCA-US 17 1578489 1578489 single base substitution G A upstream_gene_variant BRCA-US 17 1579900 1579900 single base substitution G A downstream_gene_variant BRCA-US 17 1579900 1579900 single base substitution G A exon_variant BRCA-US 17 1579900 1579900 single base substitution G A stop_gained R708* 2122C>T BRCA-US 17 1579900 1579900 single base substitution G A stop_gained R763* 2287C>T BRCA-US 17 1579900 1579900 single base substitution G A upstream_gene_variant BRCA-US 17 1579939 1579939 single base substitution A C downstream_gene_variant BRCA-US 17 1579939 1579939 single base substitution A C exon_variant BRCA-US 17 1579939 1579939 single base substitution A C missense_variant W695G 2083T>G BRCA-US 17 1579939 1579939 single base substitution A C missense_variant W750G 2248T>G BRCA-US 17 1579939 1579939 single base substitution A C upstream_gene_variant BRCA-US 17 1580872 1580872 single base substitution G T downstream_gene_variant BRCA-US 17 1580872 1580872 single base substitution G T synonymous_variant A602A 1806C>A BRCA-US 17 1580872 1580872 single base substitution G T synonymous_variant A657A 1971C>A BRCA-US 17 1580872 1580872 single base substitution G T upstream_gene_variant BRCA-US 17 1580966 1580966 single base substitution C A downstream_gene_variant BRCA-US 17 1580966 1580966 single base substitution C A missense_variant G571V 1712G>T BRCA-US 17 1580966 1580966 single base substitution C A missense_variant G626V 1877G>T BRCA-US 17 1580966 1580966 single base substitution C A upstream_gene_variant BRCA-US 17 1582137 1582137 single base substitution C T downstream_gene_variant BRCA-US 17 1582137 1582137 single base substitution C T exon_variant BRCA-US 17 1582137 1582137 single base substitution C T synonymous_variant L491L 1473G>A BRCA-US 17 1582137 1582137 single base substitution C T synonymous_variant L546L 1638G>A BRCA-US 17 1582137 1582137 single base substitution C T upstream_gene_variant BTCA-JP 17 1551327 1551327 single base substitution C T downstream_gene_variant BTCA-JP 17 1551732 1551732 single base substitution G A downstream_gene_variant BTCA-JP 17 1561824 1561824 single base substitution T C downstream_gene_variant BTCA-JP 17 1561824 1561824 single base substitution T C missense_variant H1791R 5372A>G BTCA-JP 17 1561824 1561824 single base substitution T C upstream_gene_variant BTCA-JP 17 1564663 1564663 single base substitution G A exon_variant BTCA-JP 17 1564663 1564663 single base substitution G A missense_variant R1414C 4240C>T BTCA-JP 17 1564663 1564663 single base substitution G A missense_variant R57C 169C>T BTCA-JP 17 1564663 1564663 single base substitution G A upstream_gene_variant BTCA-JP 17 1564957 1564957 single base substitution G A exon_variant BTCA-JP 17 1564957 1564957 single base substitution G A intron_variant BTCA-JP 17 1564957 1564957 single base substitution G A missense_variant R1384W 4150C>T BTCA-JP 17 1564957 1564957 single base substitution G A upstream_gene_variant BTCA-JP 17 1565493 1565493 single base substitution G A intron_variant BTCA-JP 17 1565493 1565493 single base substitution G A upstream_gene_variant BTCA-JP 17 1576947 1576947 single base substitution C T downstream_gene_variant BTCA-JP 17 1576947 1576947 single base substitution C T intron_variant BTCA-JP 17 1576947 1576947 single base substitution C T upstream_gene_variant BTCA-JP 17 1582073 1582073 single base substitution T C downstream_gene_variant BTCA-JP 17 1582073 1582073 single base substitution T C exon_variant BTCA-JP 17 1582073 1582073 single base substitution T C missense_variant N513D 1537A>G BTCA-JP 17 1582073 1582073 single base substitution T C missense_variant N568D 1702A>G BTCA-JP 17 1582073 1582073 single base substitution T C upstream_gene_variant BTCA-JP 17 1584828 1584828 single base substitution A G downstream_gene_variant BTCA-JP 17 1584828 1584828 single base substitution A G synonymous_variant N215N 645T>C BTCA-JP 17 1584828 1584828 single base substitution A G synonymous_variant N270N 810T>C BTCA-JP 17 1584828 1584828 single base substitution A G upstream_gene_variant BTCA-JP 17 1586674 1586674 single base substitution G A exon_variant BTCA-JP 17 1586674 1586674 single base substitution G A intron_variant BTCA-JP 17 1586674 1586674 single base substitution G A upstream_gene_variant BTCA-JP 17 1587792 1587792 insertion of <=200bp - A exon_variant BTCA-JP 17 1587792 1587792 insertion of <=200bp - A frameshift_variant M25I? BTCA-JP 17 1587792 1587792 insertion of <=200bp - A upstream_gene_variant CESC-US 17 1551691 1551691 single base substitution G C downstream_gene_variant CESC-US 17 1554817 1554817 single base substitution G C downstream_gene_variant CESC-US 17 1554817 1554817 single base substitution G C exon_variant CESC-US 17 1554817 1554817 single base substitution G C missense_variant Q2181E 6541C>G CESC-US 17 1554817 1554817 single base substitution G C upstream_gene_variant CESC-US 17 1554945 1554945 single base substitution G C downstream_gene_variant CESC-US 17 1554945 1554945 single base substitution G C exon_variant CESC-US 17 1554945 1554945 single base substitution G C synonymous_variant L2169L 6507C>G CESC-US 17 1554945 1554945 single base substitution G C upstream_gene_variant CESC-US 17 1556852 1556852 single base substitution G C exon_variant CESC-US 17 1556852 1556852 single base substitution G C missense_variant S2118C 6353C>G CESC-US 17 1556852 1556852 single base substitution G C upstream_gene_variant CESC-US 17 1556890 1556890 single base substitution G A exon_variant CESC-US 17 1556890 1556890 single base substitution G A synonymous_variant I2105I 6315C>T CESC-US 17 1556890 1556890 single base substitution G A upstream_gene_variant CESC-US 17 1557268 1557268 single base substitution G A exon_variant CESC-US 17 1557268 1557268 single base substitution G A synonymous_variant I2010I 6030C>T CESC-US 17 1557268 1557268 single base substitution G A upstream_gene_variant CESC-US 17 1558693 1558693 single base substitution C T downstream_gene_variant CESC-US 17 1558693 1558693 single base substitution C T missense_variant E1980K 5938G>A CESC-US 17 1558693 1558693 single base substitution C T upstream_gene_variant CESC-US 17 1560004 1560004 single base substitution G A downstream_gene_variant CESC-US 17 1560004 1560004 single base substitution G A missense_variant P1853S 5557C>T CESC-US 17 1560004 1560004 single base substitution G A upstream_gene_variant CESC-US 17 1561948 1561948 single base substitution C G downstream_gene_variant CESC-US 17 1561948 1561948 single base substitution C G missense_variant G1750R 5248G>C CESC-US 17 1561948 1561948 single base substitution C G upstream_gene_variant CLLE-ES 17 1583858 1583858 single base substitution T C downstream_gene_variant CLLE-ES 17 1583858 1583858 single base substitution T C exon_variant CLLE-ES 17 1583858 1583858 single base substitution T C intron_variant CLLE-ES 17 1583858 1583858 single base substitution T C upstream_gene_variant COAD-US 17 1557119 1557119 single base substitution C G exon_variant COAD-US 17 1557119 1557119 single base substitution C G missense_variant S2060T 6179G>C COAD-US 17 1557119 1557119 single base substitution C G upstream_gene_variant COAD-US 17 1559773 1559773 single base substitution G A downstream_gene_variant COAD-US 17 1559773 1559773 single base substitution G A synonymous_variant F1902F 5706C>T COAD-US 17 1559773 1559773 single base substitution G A upstream_gene_variant COAD-US 17 1562781 1562781 deletion of <=200bp C - downstream_gene_variant COAD-US 17 1562781 1562781 deletion of <=200bp C - exon_variant COAD-US 17 1562781 1562781 deletion of <=200bp C - frameshift_variant D1670 COAD-US 17 1562781 1562781 deletion of <=200bp C - upstream_gene_variant COAD-US 17 1576726 1576726 single base substitution G A downstream_gene_variant COAD-US 17 1576726 1576726 single base substitution G A synonymous_variant C1194C 3582C>T COAD-US 17 1576726 1576726 single base substitution G A upstream_gene_variant COAD-US 17 1577064 1577064 single base substitution C T downstream_gene_variant COAD-US 17 1577064 1577064 single base substitution C T missense_variant R1141H 3422G>A COAD-US 17 1577064 1577064 single base substitution C T upstream_gene_variant COAD-US 17 1577960 1577960 single base substitution C T downstream_gene_variant COAD-US 17 1577960 1577960 single base substitution C T exon_variant COAD-US 17 1577960 1577960 single base substitution C T synonymous_variant T1025T 3075G>A COAD-US 17 1577960 1577960 single base substitution C T synonymous_variant T970T 2910G>A COAD-US 17 1577960 1577960 single base substitution C T upstream_gene_variant COAD-US 17 1579070 1579070 single base substitution C T downstream_gene_variant COAD-US 17 1579070 1579070 single base substitution C T missense_variant V851I 2551G>A COAD-US 17 1579070 1579070 single base substitution C T missense_variant V906I 2716G>A COAD-US 17 1579070 1579070 single base substitution C T upstream_gene_variant COAD-US 17 1582908 1582908 single base substitution C A downstream_gene_variant COAD-US 17 1582908 1582908 single base substitution C A missense_variant K373N 1119G>T COAD-US 17 1582908 1582908 single base substitution C A missense_variant K428N 1284G>T COAD-US 17 1582908 1582908 single base substitution C A upstream_gene_variant COCA-CN 17 1549679 1549679 single base substitution G A downstream_gene_variant COCA-CN 17 1551699 1551699 single base substitution T C downstream_gene_variant COCA-CN 17 1554540 1554540 single base substitution G A downstream_gene_variant COCA-CN 17 1554540 1554540 single base substitution G A exon_variant COCA-CN 17 1554540 1554540 single base substitution G A missense_variant R2239C 6715C>T COCA-CN 17 1554540 1554540 single base substitution G A missense_variant R8C 22C>T COCA-CN 17 1557072 1557072 single base substitution T C missense_variant R2076G 6226A>G COCA-CN 17 1557072 1557072 single base substitution T C splice_region_variant COCA-CN 17 1557072 1557072 single base substitution T C upstream_gene_variant COCA-CN 17 1561792 1561792 single base substitution G A downstream_gene_variant COCA-CN 17 1561792 1561792 single base substitution G A intron_variant COCA-CN 17 1561792 1561792 single base substitution G A upstream_gene_variant COCA-CN 17 1576274 1576274 single base substitution G T downstream_gene_variant COCA-CN 17 1576274 1576274 single base substitution G T exon_variant COCA-CN 17 1576274 1576274 single base substitution G T intron_variant COCA-CN 17 1576923 1576923 single base substitution A G downstream_gene_variant COCA-CN 17 1576923 1576923 single base substitution A G intron_variant COCA-CN 17 1576923 1576923 single base substitution A G upstream_gene_variant COCA-CN 17 1577161 1577161 single base substitution G A downstream_gene_variant COCA-CN 17 1577161 1577161 single base substitution G A synonymous_variant L1109L 3325C>T COCA-CN 17 1577161 1577161 single base substitution G A upstream_gene_variant COCA-CN 17 1577986 1577986 single base substitution G T downstream_gene_variant COCA-CN 17 1577986 1577986 single base substitution G T intron_variant COCA-CN 17 1577986 1577986 single base substitution G T upstream_gene_variant COCA-CN 17 1579337 1579337 single base substitution C T downstream_gene_variant COCA-CN 17 1579337 1579337 single base substitution C T missense_variant R800Q 2399G>A COCA-CN 17 1579337 1579337 single base substitution C T missense_variant R855Q 2564G>A COCA-CN 17 1579337 1579337 single base substitution C T upstream_gene_variant COCA-CN 17 1579793 1579793 single base substitution C T downstream_gene_variant COCA-CN 17 1579793 1579793 single base substitution C T splice_region_variant COCA-CN 17 1579793 1579793 single base substitution C T upstream_gene_variant COCA-CN 17 1582649 1582649 single base substitution T G downstream_gene_variant COCA-CN 17 1582649 1582649 single base substitution T G missense_variant K394Q 1180A>C COCA-CN 17 1582649 1582649 single base substitution T G missense_variant K449Q 1345A>C COCA-CN 17 1582649 1582649 single base substitution T G upstream_gene_variant COCA-CN 17 1582955 1582955 single base substitution G T downstream_gene_variant COCA-CN 17 1582955 1582955 single base substitution G T missense_variant L358I 1072C>A COCA-CN 17 1582955 1582955 single base substitution G T missense_variant L413I 1237C>A COCA-CN 17 1582955 1582955 single base substitution G T upstream_gene_variant COCA-CN 17 1584005 1584005 single base substitution C A downstream_gene_variant COCA-CN 17 1584005 1584005 single base substitution C A exon_variant COCA-CN 17 1584005 1584005 single base substitution C A intron_variant COCA-CN 17 1584005 1584005 single base substitution C A upstream_gene_variant COCA-CN 17 1584954 1584954 single base substitution C T downstream_gene_variant COCA-CN 17 1584954 1584954 single base substitution C T stop_gained W173* 519G>A COCA-CN 17 1584954 1584954 single base substitution C T stop_gained W228* 684G>A COCA-CN 17 1584954 1584954 single base substitution C T upstream_gene_variant EOPC-DE 17 1553905 1553905 single base substitution A C downstream_gene_variant EOPC-DE 17 1573611 1573611 single base substitution T C downstream_gene_variant EOPC-DE 17 1573611 1573611 single base substitution T C intron_variant ESAD-UK 17 1549586 1549586 single base substitution C A downstream_gene_variant ESAD-UK 17 1554427 1554427 single base substitution C A downstream_gene_variant ESAD-UK 17 1554427 1554427 single base substitution C A exon_variant ESAD-UK 17 1554427 1554427 single base substitution C A missense_variant Q2276H 6828G>T ESAD-UK 17 1554427 1554427 single base substitution C A missense_variant Q45H 135G>T ESAD-UK 17 1560592 1560592 single base substitution C T downstream_gene_variant ESAD-UK 17 1560592 1560592 single base substitution C T intron_variant ESAD-UK 17 1560592 1560592 single base substitution C T upstream_gene_variant ESAD-UK 17 1563364 1563364 single base substitution A T downstream_gene_variant ESAD-UK 17 1563364 1563364 single base substitution A T intron_variant ESAD-UK 17 1564663 1564663 single base substitution G A exon_variant ESAD-UK 17 1564663 1564663 single base substitution G A missense_variant R1414C 4240C>T ESAD-UK 17 1564663 1564663 single base substitution G A missense_variant R57C 169C>T ESAD-UK 17 1564663 1564663 single base substitution G A upstream_gene_variant ESAD-UK 17 1565420 1565420 single base substitution T G missense_variant I1268L 3802A>C ESAD-UK 17 1565420 1565420 single base substitution T G upstream_gene_variant ESAD-UK 17 1566420 1566420 single base substitution G A intron_variant ESAD-UK 17 1566420 1566420 single base substitution G A upstream_gene_variant ESAD-UK 17 1567500 1567500 deletion of <=200bp T - intron_variant ESAD-UK 17 1567500 1567500 deletion of <=200bp T - upstream_gene_variant ESAD-UK 17 1568908 1568908 single base substitution C A intron_variant ESAD-UK 17 1568908 1568908 single base substitution C A upstream_gene_variant ESAD-UK 17 1569392 1569392 single base substitution G A intron_variant ESAD-UK 17 1569392 1569392 single base substitution G A upstream_gene_variant ESAD-UK 17 1571541 1571541 single base substitution A C downstream_gene_variant ESAD-UK 17 1571541 1571541 single base substitution A C intron_variant ESAD-UK 17 1571543 1571543 single base substitution T G downstream_gene_variant ESAD-UK 17 1571543 1571543 single base substitution T G intron_variant ESAD-UK 17 1572209 1572209 single base substitution A G downstream_gene_variant ESAD-UK 17 1572209 1572209 single base substitution A G intron_variant ESAD-UK 17 1575076 1575076 single base substitution C T downstream_gene_variant ESAD-UK 17 1575076 1575076 single base substitution C T intron_variant ESAD-UK 17 1578397 1578397 single base substitution C G downstream_gene_variant ESAD-UK 17 1578397 1578397 single base substitution C G intron_variant ESAD-UK 17 1578397 1578397 single base substitution C G upstream_gene_variant ESAD-UK 17 1579208 1579208 single base substitution G A downstream_gene_variant ESAD-UK 17 1579208 1579208 single base substitution G A intron_variant ESAD-UK 17 1579208 1579208 single base substitution G A upstream_gene_variant ESAD-UK 17 1582417 1582417 single base substitution C T downstream_gene_variant ESAD-UK 17 1582417 1582417 single base substitution C T exon_variant ESAD-UK 17 1582417 1582417 single base substitution C T missense_variant R443H 1328G>A ESAD-UK 17 1582417 1582417 single base substitution C T missense_variant R498H 1493G>A ESAD-UK 17 1582417 1582417 single base substitution C T upstream_gene_variant ESAD-UK 17 1582817 1582817 deletion of <=200bp A - downstream_gene_variant ESAD-UK 17 1582817 1582817 deletion of <=200bp A - intron_variant ESAD-UK 17 1582817 1582817 deletion of <=200bp A - upstream_gene_variant ESAD-UK 17 1583490 1583490 single base substitution C T downstream_gene_variant ESAD-UK 17 1583490 1583490 single base substitution C T intron_variant ESAD-UK 17 1583490 1583490 single base substitution C T upstream_gene_variant ESAD-UK 17 1587799 1587799 single base substitution C A exon_variant ESAD-UK 17 1587799 1587799 single base substitution C A missense_variant D23Y 67G>T ESAD-UK 17 1587799 1587799 single base substitution C A upstream_gene_variant ESAD-UK 17 1588027 1588027 single base substitution A G 5_prime_UTR_variant ESAD-UK 17 1588027 1588027 single base substitution A G intron_variant ESAD-UK 17 1588027 1588027 single base substitution A G upstream_gene_variant ESAD-UK 17 1590486 1590486 single base substitution C A upstream_gene_variant ESCA-CN 17 1561625 1561625 single base substitution G A downstream_gene_variant ESCA-CN 17 1561625 1561625 single base substitution G A synonymous_variant I1809I 5427C>T ESCA-CN 17 1561625 1561625 single base substitution G A upstream_gene_variant ESCA-CN 17 1563672 1563672 single base substitution A G downstream_gene_variant ESCA-CN 17 1563672 1563672 single base substitution A G intron_variant ESCA-CN 17 1585425 1585425 single base substitution C A downstream_gene_variant ESCA-CN 17 1585425 1585425 single base substitution C A intron_variant ESCA-CN 17 1585425 1585425 single base substitution C A missense_variant W144C 432G>T ESCA-CN 17 1585425 1585425 single base substitution C A upstream_gene_variant GBM-US 17 1551765 1551765 single base substitution G T downstream_gene_variant GBM-US 17 1577046 1577046 single base substitution A G downstream_gene_variant GBM-US 17 1577046 1577046 single base substitution A G missense_variant V1147A 3440T>C GBM-US 17 1577046 1577046 single base substitution A G upstream_gene_variant GBM-US 17 1577829 1577829 single base substitution T C downstream_gene_variant GBM-US 17 1577829 1577829 single base substitution T C missense_variant N1069S 3206A>G GBM-US 17 1577829 1577829 single base substitution T C upstream_gene_variant KIRC-US 17 1549792 1549792 single base substitution A T downstream_gene_variant KIRC-US 17 1559850 1559855 deletion of <=200bp GTAAGT - disruptive_inframe_deletion HLL1875L KIRC-US 17 1559850 1559855 deletion of <=200bp GTAAGT - downstream_gene_variant KIRC-US 17 1559850 1559855 deletion of <=200bp GTAAGT - upstream_gene_variant KIRC-US 17 1559949 1559949 single base substitution G A downstream_gene_variant KIRC-US 17 1559949 1559949 single base substitution G A missense_variant P1871L 5612C>T KIRC-US 17 1559949 1559949 single base substitution G A upstream_gene_variant KIRC-US 17 1564002 1564002 single base substitution T A downstream_gene_variant KIRC-US 17 1564002 1564002 single base substitution T A exon_variant KIRC-US 17 1564002 1564002 single base substitution T A missense_variant N1543I 4628A>T KIRC-US 17 1564002 1564002 single base substitution T A missense_variant N186I 557A>T KIRC-US 17 1579248 1579248 single base substitution G A downstream_gene_variant KIRC-US 17 1579248 1579248 single base substitution G A missense_variant L830F 2488C>T KIRC-US 17 1579248 1579248 single base substitution G A missense_variant L885F 2653C>T KIRC-US 17 1579248 1579248 single base substitution G A upstream_gene_variant KIRC-US 17 1582621 1582621 single base substitution G A downstream_gene_variant KIRC-US 17 1582621 1582621 single base substitution G A missense_variant A403V 1208C>T KIRC-US 17 1582621 1582621 single base substitution G A missense_variant A458V 1373C>T KIRC-US 17 1582621 1582621 single base substitution G A upstream_gene_variant KIRC-US 17 1584776 1584776 single base substitution G C downstream_gene_variant KIRC-US 17 1584776 1584776 single base substitution G C missense_variant L233V 697C>G KIRC-US 17 1584776 1584776 single base substitution G C missense_variant L288V 862C>G KIRC-US 17 1584776 1584776 single base substitution G C upstream_gene_variant KIRC-US 17 1586888 1586888 single base substitution T G exon_variant KIRC-US 17 1586888 1586888 single base substitution T G missense_variant I70L 208A>C KIRC-US 17 1586888 1586888 single base substitution T G upstream_gene_variant KIRP-US 17 1564455 1564455 single base substitution A T exon_variant KIRP-US 17 1564455 1564455 single base substitution A T missense_variant V1447D 4340T>A KIRP-US 17 1564455 1564455 single base substitution A T missense_variant V90D 269T>A KIRP-US 17 1564455 1564455 single base substitution A T splice_region_variant KIRP-US 17 1585300 1585300 insertion of <=200bp - T downstream_gene_variant KIRP-US 17 1585300 1585300 insertion of <=200bp - T frameshift_variant R101R? KIRP-US 17 1585300 1585300 insertion of <=200bp - T frameshift_variant R156R? KIRP-US 17 1585300 1585300 insertion of <=200bp - T upstream_gene_variant KIRP-US 17 1586885 1586885 single base substitution G C exon_variant KIRP-US 17 1586885 1586885 single base substitution G C missense_variant R71G 211C>G KIRP-US 17 1586885 1586885 single base substitution G C upstream_gene_variant LAML-KR 17 1559230 1559230 single base substitution T C downstream_gene_variant LAML-KR 17 1559230 1559230 single base substitution T C intron_variant LAML-KR 17 1559230 1559230 single base substitution T C upstream_gene_variant LAML-KR 17 1590802 1590802 single base substitution C T upstream_gene_variant LAML-KR 17 1590803 1590803 single base substitution A G upstream_gene_variant LAML-KR 17 1593122 1593122 single base substitution G A upstream_gene_variant LGG-US 17 1557307 1557307 single base substitution C T exon_variant LGG-US 17 1557307 1557307 single base substitution C T synonymous_variant V1997V 5991G>A LGG-US 17 1557307 1557307 single base substitution C T upstream_gene_variant LGG-US 17 1577065 1577065 single base substitution G A downstream_gene_variant LGG-US 17 1577065 1577065 single base substitution G A missense_variant R1141C 3421C>T LGG-US 17 1577065 1577065 single base substitution G A upstream_gene_variant LGG-US 17 1578465 1578465 single base substitution T C downstream_gene_variant LGG-US 17 1578465 1578465 single base substitution T C exon_variant LGG-US 17 1578465 1578465 single base substitution T C missense_variant N1014S 3041A>G LGG-US 17 1578465 1578465 single base substitution T C missense_variant N959S 2876A>G LGG-US 17 1578465 1578465 single base substitution T C upstream_gene_variant LGG-US 17 1585131 1585131 single base substitution C T downstream_gene_variant LGG-US 17 1585131 1585131 single base substitution C T synonymous_variant P157P 471G>A LGG-US 17 1585131 1585131 single base substitution C T synonymous_variant P212P 636G>A LGG-US 17 1585131 1585131 single base substitution C T upstream_gene_variant LICA-CN 17 1556964 1556964 single base substitution C A exon_variant LICA-CN 17 1556964 1556964 single base substitution C A missense_variant A2081S 6241G>T LICA-CN 17 1556964 1556964 single base substitution C A upstream_gene_variant LICA-CN 17 1559972 1559972 single base substitution G A downstream_gene_variant LICA-CN 17 1559972 1559972 single base substitution G A synonymous_variant V1863V 5589C>T LICA-CN 17 1559972 1559972 single base substitution G A upstream_gene_variant LICA-FR 17 1579560 1579560 single base substitution G C downstream_gene_variant LICA-FR 17 1579560 1579560 single base substitution G C synonymous_variant S776S 2328C>G LICA-FR 17 1579560 1579560 single base substitution G C synonymous_variant S831S 2493C>G LICA-FR 17 1579560 1579560 single base substitution G C upstream_gene_variant LIHC-US 17 1549897 1549897 single base substitution G A downstream_gene_variant LIHC-US 17 1554786 1554786 single base substitution T C downstream_gene_variant LIHC-US 17 1554786 1554786 single base substitution T C exon_variant LIHC-US 17 1554786 1554786 single base substitution T C missense_variant Q2191R 6572A>G LIHC-US 17 1554786 1554786 single base substitution T C upstream_gene_variant LIHC-US 17 1561917 1561917 single base substitution T A downstream_gene_variant LIHC-US 17 1561917 1561917 single base substitution T A missense_variant E1760V 5279A>T LIHC-US 17 1561917 1561917 single base substitution T A upstream_gene_variant LIHC-US 17 1564062 1564062 single base substitution C A downstream_gene_variant LIHC-US 17 1564062 1564062 single base substitution C A exon_variant LIHC-US 17 1564062 1564062 single base substitution C A missense_variant R1523L 4568G>T LIHC-US 17 1564062 1564062 single base substitution C A missense_variant R166L 497G>T LIHC-US 17 1564444 1564444 single base substitution T C exon_variant LIHC-US 17 1564444 1564444 single base substitution T C missense_variant N1451D 4351A>G LIHC-US 17 1564444 1564444 single base substitution T C missense_variant N94D 280A>G LIHC-US 17 1576479 1576479 single base substitution G A downstream_gene_variant LIHC-US 17 1576479 1576479 single base substitution G A exon_variant LIHC-US 17 1576479 1576479 single base substitution G A missense_variant R1224C 3670C>T LIHC-US 17 1580416 1580416 single base substitution A T downstream_gene_variant LIHC-US 17 1580416 1580416 single base substitution A T exon_variant LIHC-US 17 1580416 1580416 single base substitution A T missense_variant S624T 1870T>A LIHC-US 17 1580416 1580416 single base substitution A T missense_variant S679T 2035T>A LIHC-US 17 1580416 1580416 single base substitution A T upstream_gene_variant LINC-JP 17 1565296 1565296 single base substitution C A missense_variant S12I 35G>T LINC-JP 17 1565296 1565296 single base substitution C A missense_variant S1309I 3926G>T LINC-JP 17 1565296 1565296 single base substitution C A upstream_gene_variant LINC-JP 17 1565759 1565759 single base substitution T A intron_variant LINC-JP 17 1565759 1565759 single base substitution T A upstream_gene_variant LINC-JP 17 1574230 1574230 deletion of <=200bp A - downstream_gene_variant LINC-JP 17 1574230 1574230 deletion of <=200bp A - intron_variant LINC-JP 17 1577295 1577295 single base substitution T C downstream_gene_variant LINC-JP 17 1577295 1577295 single base substitution T C intron_variant LINC-JP 17 1577295 1577295 single base substitution T C upstream_gene_variant LINC-JP 17 1580371 1580371 single base substitution G C downstream_gene_variant LINC-JP 17 1580371 1580371 single base substitution G C exon_variant LINC-JP 17 1580371 1580371 single base substitution G C missense_variant L639V 1915C>G LINC-JP 17 1580371 1580371 single base substitution G C missense_variant L694V 2080C>G LINC-JP 17 1580371 1580371 single base substitution G C upstream_gene_variant LINC-JP 17 1580469 1580469 single base substitution G T downstream_gene_variant LINC-JP 17 1580469 1580469 single base substitution G T exon_variant LINC-JP 17 1580469 1580469 single base substitution G T splice_region_variant LINC-JP 17 1580469 1580469 single base substitution G T upstream_gene_variant LINC-JP 17 1580475 1580475 single base substitution A G downstream_gene_variant LINC-JP 17 1580475 1580475 single base substitution A G exon_variant LINC-JP 17 1580475 1580475 single base substitution A G intron_variant LINC-JP 17 1580475 1580475 single base substitution A G upstream_gene_variant LINC-JP 17 1582654 1582654 single base substitution T C downstream_gene_variant LINC-JP 17 1582654 1582654 single base substitution T C missense_variant Y392C 1175A>G LINC-JP 17 1582654 1582654 single base substitution T C missense_variant Y447C 1340A>G LINC-JP 17 1582654 1582654 single base substitution T C upstream_gene_variant LIRI-JP 17 1549778 1549778 single base substitution G A downstream_gene_variant LIRI-JP 17 1550948 1550948 single base substitution A C downstream_gene_variant LIRI-JP 17 1553238 1553238 single base substitution A G downstream_gene_variant LIRI-JP 17 1554860 1554860 single base substitution A T downstream_gene_variant LIRI-JP 17 1554860 1554860 single base substitution A T intron_variant LIRI-JP 17 1554860 1554860 single base substitution A T upstream_gene_variant LIRI-JP 17 1560559 1560559 single base substitution T C downstream_gene_variant LIRI-JP 17 1560559 1560559 single base substitution T C intron_variant LIRI-JP 17 1560559 1560559 single base substitution T C upstream_gene_variant LIRI-JP 17 1561336 1561336 single base substitution A G downstream_gene_variant LIRI-JP 17 1561336 1561336 single base substitution A G intron_variant LIRI-JP 17 1561336 1561336 single base substitution A G upstream_gene_variant LIRI-JP 17 1564899 1564899 single base substitution G A intron_variant LIRI-JP 17 1564899 1564899 single base substitution G A splice_region_variant LIRI-JP 17 1564899 1564899 single base substitution G A upstream_gene_variant LIRI-JP 17 1566361 1566361 single base substitution T C intron_variant LIRI-JP 17 1566361 1566361 single base substitution T C upstream_gene_variant LIRI-JP 17 1567602 1567602 single base substitution C T intron_variant LIRI-JP 17 1567602 1567602 single base substitution C T upstream_gene_variant LIRI-JP 17 1570223 1570223 single base substitution C T intron_variant LIRI-JP 17 1570223 1570223 single base substitution C T upstream_gene_variant LIRI-JP 17 1574262 1574262 single base substitution A C downstream_gene_variant LIRI-JP 17 1574262 1574262 single base substitution A C intron_variant LIRI-JP 17 1574606 1574606 single base substitution A C downstream_gene_variant LIRI-JP 17 1574606 1574606 single base substitution A C intron_variant LIRI-JP 17 1575101 1575101 single base substitution C T downstream_gene_variant LIRI-JP 17 1575101 1575101 single base substitution C T intron_variant LIRI-JP 17 1575762 1575762 single base substitution C A downstream_gene_variant LIRI-JP 17 1575762 1575762 single base substitution C A intron_variant LIRI-JP 17 1578523 1578523 single base substitution T A downstream_gene_variant LIRI-JP 17 1578523 1578523 single base substitution T A exon_variant LIRI-JP 17 1578523 1578523 single base substitution T A missense_variant R940W 2818A>T LIRI-JP 17 1578523 1578523 single base substitution T A missense_variant R995W 2983A>T LIRI-JP 17 1578523 1578523 single base substitution T A upstream_gene_variant LIRI-JP 17 1578861 1578861 single base substitution T C downstream_gene_variant LIRI-JP 17 1578861 1578861 single base substitution T C intron_variant LIRI-JP 17 1578861 1578861 single base substitution T C upstream_gene_variant LIRI-JP 17 1581189 1581189 single base substitution A C downstream_gene_variant LIRI-JP 17 1581189 1581189 single base substitution A C intron_variant LIRI-JP 17 1581189 1581189 single base substitution A C upstream_gene_variant LIRI-JP 17 1582115 1582115 single base substitution T C downstream_gene_variant LIRI-JP 17 1582115 1582115 single base substitution T C exon_variant LIRI-JP 17 1582115 1582115 single base substitution T C missense_variant T499A 1495A>G LIRI-JP 17 1582115 1582115 single base substitution T C missense_variant T554A 1660A>G LIRI-JP 17 1582115 1582115 single base substitution T C upstream_gene_variant LIRI-JP 17 1583328 1583328 single base substitution A C downstream_gene_variant LIRI-JP 17 1583328 1583328 single base substitution A C intron_variant LIRI-JP 17 1583328 1583328 single base substitution A C upstream_gene_variant LIRI-JP 17 1583805 1583805 single base substitution A G downstream_gene_variant LIRI-JP 17 1583805 1583805 single base substitution A G exon_variant LIRI-JP 17 1583805 1583805 single base substitution A G intron_variant LIRI-JP 17 1583805 1583805 single base substitution A G upstream_gene_variant LIRI-JP 17 1588561 1588561 single base substitution G T upstream_gene_variant LIRI-JP 17 1592177 1592177 single base substitution G T upstream_gene_variant LUSC-KR 17 1553397 1553397 single base substitution C T downstream_gene_variant LUSC-KR 17 1554713 1554713 single base substitution T C downstream_gene_variant LUSC-KR 17 1554713 1554713 single base substitution T C exon_variant LUSC-KR 17 1554713 1554713 single base substitution T C synonymous_variant T2215T 6645A>G LUSC-KR 17 1554713 1554713 single base substitution T C upstream_gene_variant LUSC-KR 17 1559054 1559054 single base substitution G A downstream_gene_variant LUSC-KR 17 1559054 1559054 single base substitution G A intron_variant LUSC-KR 17 1559054 1559054 single base substitution G A upstream_gene_variant LUSC-KR 17 1559056 1559056 single base substitution G A downstream_gene_variant LUSC-KR 17 1559056 1559056 single base substitution G A intron_variant LUSC-KR 17 1559056 1559056 single base substitution G A upstream_gene_variant LUSC-KR 17 1563933 1563933 single base substitution C T downstream_gene_variant LUSC-KR 17 1563933 1563933 single base substitution C T intron_variant LUSC-KR 17 1567382 1567382 single base substitution T C intron_variant LUSC-KR 17 1567382 1567382 single base substitution T C upstream_gene_variant LUSC-KR 17 1570380 1570380 single base substitution T C intron_variant LUSC-KR 17 1572274 1572274 single base substitution T A downstream_gene_variant LUSC-KR 17 1572274 1572274 single base substitution T A intron_variant LUSC-KR 17 1577206 1577206 single base substitution C A downstream_gene_variant LUSC-KR 17 1577206 1577206 single base substitution C A intron_variant LUSC-KR 17 1577206 1577206 single base substitution C A upstream_gene_variant LUSC-KR 17 1582570 1582570 single base substitution C G downstream_gene_variant LUSC-KR 17 1582570 1582570 single base substitution C G intron_variant LUSC-KR 17 1582570 1582570 single base substitution C G upstream_gene_variant LUSC-KR 17 1591446 1591446 single base substitution C A upstream_gene_variant LUSC-KR 17 1592145 1592145 single base substitution G C upstream_gene_variant LUSC-KR 17 1592729 1592729 single base substitution C T upstream_gene_variant LUSC-KR 17 1592831 1592831 single base substitution T C upstream_gene_variant LUSC-US 17 1551211 1551211 single base substitution C T downstream_gene_variant LUSC-US 17 1554484 1554484 single base substitution C G downstream_gene_variant LUSC-US 17 1554484 1554484 single base substitution C G exon_variant LUSC-US 17 1554484 1554484 single base substitution C G missense_variant E2257D 6771G>C LUSC-US 17 1554484 1554484 single base substitution C G missense_variant E26D 78G>C LUSC-US 17 1577070 1577070 single base substitution C A downstream_gene_variant LUSC-US 17 1577070 1577070 single base substitution C A missense_variant R1139L 3416G>T LUSC-US 17 1577070 1577070 single base substitution C A upstream_gene_variant LUSC-US 17 1582317 1582317 single base substitution G A downstream_gene_variant LUSC-US 17 1582317 1582317 single base substitution G A exon_variant LUSC-US 17 1582317 1582317 single base substitution G A synonymous_variant T476T 1428C>T LUSC-US 17 1582317 1582317 single base substitution G A synonymous_variant T531T 1593C>T LUSC-US 17 1582317 1582317 single base substitution G A upstream_gene_variant LUSC-US 17 1582619 1582619 single base substitution G C downstream_gene_variant LUSC-US 17 1582619 1582619 single base substitution G C missense_variant L404V 1210C>G LUSC-US 17 1582619 1582619 single base substitution G C missense_variant L459V 1375C>G LUSC-US 17 1582619 1582619 single base substitution G C upstream_gene_variant LUSC-US 17 1582704 1582704 single base substitution C G downstream_gene_variant LUSC-US 17 1582704 1582704 single base substitution C G missense_variant W375C 1125G>C LUSC-US 17 1582704 1582704 single base substitution C G missense_variant W430C 1290G>C LUSC-US 17 1582704 1582704 single base substitution C G upstream_gene_variant LUSC-US 17 1584337 1584337 single base substitution C A downstream_gene_variant LUSC-US 17 1584337 1584337 single base substitution C A exon_variant LUSC-US 17 1584337 1584337 single base substitution C A missense_variant W238L 713G>T LUSC-US 17 1584337 1584337 single base substitution C A missense_variant W293L 878G>T LUSC-US 17 1584337 1584337 single base substitution C A upstream_gene_variant LUSC-US 17 1585180 1585180 single base substitution T A downstream_gene_variant LUSC-US 17 1585180 1585180 single base substitution T A missense_variant D141V 422A>T LUSC-US 17 1585180 1585180 single base substitution T A missense_variant D196V 587A>T LUSC-US 17 1585180 1585180 single base substitution T A upstream_gene_variant LUSC-US 17 1585256 1585256 single base substitution C A downstream_gene_variant LUSC-US 17 1585256 1585256 single base substitution C A missense_variant D116Y 346G>T LUSC-US 17 1585256 1585256 single base substitution C A missense_variant D171Y 511G>T LUSC-US 17 1585256 1585256 single base substitution C A upstream_gene_variant MALY-DE 17 1557687 1557687 single base substitution G C exon_variant MALY-DE 17 1557687 1557687 single base substitution G C intron_variant MALY-DE 17 1557687 1557687 single base substitution G C upstream_gene_variant MALY-DE 17 1558316 1558316 deletion of <=200bp G - downstream_gene_variant MALY-DE 17 1558316 1558316 deletion of <=200bp G - intron_variant MALY-DE 17 1558316 1558316 deletion of <=200bp G - upstream_gene_variant MALY-DE 17 1567477 1567477 single base substitution A T intron_variant MALY-DE 17 1567477 1567477 single base substitution A T upstream_gene_variant MALY-DE 17 1567478 1567478 single base substitution C T intron_variant MALY-DE 17 1567478 1567478 single base substitution C T upstream_gene_variant MALY-DE 17 1575995 1575995 single base substitution C T downstream_gene_variant MALY-DE 17 1575995 1575995 single base substitution C T intron_variant MALY-DE 17 1577385 1577385 single base substitution C T downstream_gene_variant MALY-DE 17 1577385 1577385 single base substitution C T intron_variant MALY-DE 17 1577385 1577385 single base substitution C T upstream_gene_variant MALY-DE 17 1580231 1580231 single base substitution C T downstream_gene_variant MALY-DE 17 1580231 1580231 single base substitution C T intron_variant MALY-DE 17 1580231 1580231 single base substitution C T upstream_gene_variant MALY-DE 17 1580880 1580880 single base substitution G A downstream_gene_variant MALY-DE 17 1580880 1580880 single base substitution G A missense_variant L600F 1798C>T MALY-DE 17 1580880 1580880 single base substitution G A missense_variant L655F 1963C>T MALY-DE 17 1580880 1580880 single base substitution G A upstream_gene_variant MALY-DE 17 1591573 1591573 single base substitution T C upstream_gene_variant MELA-AU 17 1549598 1549598 insertion of <=200bp - CT downstream_gene_variant MELA-AU 17 1549607 1549607 single base substitution G A downstream_gene_variant MELA-AU 17 1549965 1549965 single base substitution G A downstream_gene_variant MELA-AU 17 1550160 1550160 single base substitution C G downstream_gene_variant MELA-AU 17 1550335 1550335 single base substitution G A downstream_gene_variant MELA-AU 17 1552448 1552449 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 17 1553530 1553530 single base substitution G T downstream_gene_variant MELA-AU 17 1554257 1554257 single base substitution G A downstream_gene_variant MELA-AU 17 1554257 1554257 single base substitution G A intron_variant MELA-AU 17 1554772 1554772 single base substitution G A downstream_gene_variant MELA-AU 17 1554772 1554772 single base substitution G A exon_variant MELA-AU 17 1554772 1554772 single base substitution G A missense_variant H2196Y 6586C>T MELA-AU 17 1554772 1554772 single base substitution G A upstream_gene_variant MELA-AU 17 1555719 1555719 single base substitution G A downstream_gene_variant MELA-AU 17 1555719 1555719 single base substitution G A intron_variant MELA-AU 17 1555719 1555719 single base substitution G A upstream_gene_variant MELA-AU 17 1555755 1555755 single base substitution A G downstream_gene_variant MELA-AU 17 1555755 1555755 single base substitution A G intron_variant MELA-AU 17 1555755 1555755 single base substitution A G upstream_gene_variant MELA-AU 17 1556212 1556212 single base substitution G A exon_variant MELA-AU 17 1556212 1556212 single base substitution G A intron_variant MELA-AU 17 1556212 1556212 single base substitution G A upstream_gene_variant MELA-AU 17 1556534 1556534 single base substitution G A exon_variant MELA-AU 17 1556534 1556534 single base substitution G A intron_variant MELA-AU 17 1556534 1556534 single base substitution G A upstream_gene_variant MELA-AU 17 1556593 1556594 multiple base substitution (>=2bp and <=200bp) CC TT exon_variant MELA-AU 17 1556593 1556594 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 17 1556593 1556594 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 17 1557542 1557542 single base substitution C T exon_variant MELA-AU 17 1557542 1557542 single base substitution C T intron_variant MELA-AU 17 1557542 1557542 single base substitution C T upstream_gene_variant MELA-AU 17 1558020 1558020 single base substitution G A downstream_gene_variant MELA-AU 17 1558020 1558020 single base substitution G A exon_variant MELA-AU 17 1558020 1558020 single base substitution G A intron_variant MELA-AU 17 1558020 1558020 single base substitution G A upstream_gene_variant MELA-AU 17 1558368 1558368 single base substitution C A downstream_gene_variant MELA-AU 17 1558368 1558368 single base substitution C A intron_variant MELA-AU 17 1558368 1558368 single base substitution C A upstream_gene_variant MELA-AU 17 1558847 1558847 single base substitution G A downstream_gene_variant MELA-AU 17 1558847 1558847 single base substitution G A intron_variant MELA-AU 17 1558847 1558847 single base substitution G A upstream_gene_variant MELA-AU 17 1559376 1559376 single base substitution G A downstream_gene_variant MELA-AU 17 1559376 1559376 single base substitution G A intron_variant MELA-AU 17 1559376 1559376 single base substitution G A upstream_gene_variant MELA-AU 17 1559435 1559435 single base substitution T A downstream_gene_variant MELA-AU 17 1559435 1559435 single base substitution T A intron_variant MELA-AU 17 1559435 1559435 single base substitution T A upstream_gene_variant MELA-AU 17 1559486 1559486 single base substitution G A downstream_gene_variant MELA-AU 17 1559486 1559486 single base substitution G A intron_variant MELA-AU 17 1559486 1559486 single base substitution G A upstream_gene_variant MELA-AU 17 1560080 1560080 single base substitution G A downstream_gene_variant MELA-AU 17 1560080 1560080 single base substitution G A intron_variant MELA-AU 17 1560080 1560080 single base substitution G A upstream_gene_variant MELA-AU 17 1560713 1560713 single base substitution G A downstream_gene_variant MELA-AU 17 1560713 1560713 single base substitution G A intron_variant MELA-AU 17 1560713 1560713 single base substitution G A upstream_gene_variant MELA-AU 17 1560917 1560917 single base substitution G A downstream_gene_variant MELA-AU 17 1560917 1560917 single base substitution G A intron_variant MELA-AU 17 1560917 1560917 single base substitution G A upstream_gene_variant MELA-AU 17 1561183 1561183 single base substitution T C downstream_gene_variant MELA-AU 17 1561183 1561183 single base substitution T C intron_variant MELA-AU 17 1561183 1561183 single base substitution T C upstream_gene_variant MELA-AU 17 1562289 1562289 single base substitution G A downstream_gene_variant MELA-AU 17 1562289 1562289 single base substitution G A intron_variant MELA-AU 17 1562289 1562289 single base substitution G A upstream_gene_variant MELA-AU 17 1563125 1563125 single base substitution A C downstream_gene_variant MELA-AU 17 1563125 1563125 single base substitution A C exon_variant MELA-AU 17 1563125 1563125 single base substitution A C intron_variant MELA-AU 17 1563125 1563125 single base substitution A C upstream_gene_variant MELA-AU 17 1563291 1563291 single base substitution A G downstream_gene_variant MELA-AU 17 1563291 1563291 single base substitution A G exon_variant MELA-AU 17 1563291 1563291 single base substitution A G missense_variant F1597S 4790T>C MELA-AU 17 1563291 1563291 single base substitution A G missense_variant F240S 719T>C MELA-AU 17 1564110 1564110 single base substitution C A downstream_gene_variant MELA-AU 17 1564110 1564110 single base substitution C A exon_variant MELA-AU 17 1564110 1564110 single base substitution C A missense_variant S1507I 4520G>T MELA-AU 17 1564110 1564110 single base substitution C A missense_variant S150I 449G>T MELA-AU 17 1564525 1564525 single base substitution G A exon_variant MELA-AU 17 1564525 1564525 single base substitution G A intron_variant MELA-AU 17 1564602 1564602 single base substitution T C exon_variant MELA-AU 17 1564602 1564602 single base substitution T C missense_variant K1434R 4301A>G MELA-AU 17 1564602 1564602 single base substitution T C missense_variant K77R 230A>G MELA-AU 17 1566711 1566711 single base substitution G A intron_variant MELA-AU 17 1566711 1566711 single base substitution G A upstream_gene_variant MELA-AU 17 1568846 1568846 single base substitution G T intron_variant MELA-AU 17 1568846 1568846 single base substitution G T upstream_gene_variant MELA-AU 17 1569184 1569184 single base substitution G A intron_variant MELA-AU 17 1569184 1569184 single base substitution G A upstream_gene_variant MELA-AU 17 1569417 1569417 single base substitution G A intron_variant MELA-AU 17 1569417 1569417 single base substitution G A upstream_gene_variant MELA-AU 17 1570254 1570254 single base substitution G A intron_variant MELA-AU 17 1570254 1570254 single base substitution G A upstream_gene_variant MELA-AU 17 1570286 1570286 single base substitution G A intron_variant MELA-AU 17 1570286 1570286 single base substitution G A upstream_gene_variant MELA-AU 17 1571201 1571201 single base substitution G A intron_variant MELA-AU 17 1571529 1571529 single base substitution C T downstream_gene_variant MELA-AU 17 1571529 1571529 single base substitution C T intron_variant MELA-AU 17 1572464 1572464 single base substitution G A downstream_gene_variant MELA-AU 17 1572464 1572464 single base substitution G A intron_variant MELA-AU 17 1572521 1572521 single base substitution C T downstream_gene_variant MELA-AU 17 1572521 1572521 single base substitution C T intron_variant MELA-AU 17 1572656 1572656 single base substitution C T downstream_gene_variant MELA-AU 17 1572656 1572656 single base substitution C T intron_variant MELA-AU 17 1573583 1573583 single base substitution A C downstream_gene_variant MELA-AU 17 1573583 1573583 single base substitution A C intron_variant MELA-AU 17 1574102 1574102 single base substitution G A downstream_gene_variant MELA-AU 17 1574102 1574102 single base substitution G A intron_variant MELA-AU 17 1574239 1574239 single base substitution A G downstream_gene_variant MELA-AU 17 1574239 1574239 single base substitution A G intron_variant MELA-AU 17 1574741 1574741 single base substitution G A downstream_gene_variant MELA-AU 17 1574741 1574741 single base substitution G A intron_variant MELA-AU 17 1575239 1575239 single base substitution G A downstream_gene_variant MELA-AU 17 1575239 1575239 single base substitution G A intron_variant MELA-AU 17 1575625 1575625 single base substitution G A downstream_gene_variant MELA-AU 17 1575625 1575625 single base substitution G A intron_variant MELA-AU 17 1575792 1575792 single base substitution G A downstream_gene_variant MELA-AU 17 1575792 1575792 single base substitution G A intron_variant MELA-AU 17 1575962 1575962 single base substitution C T downstream_gene_variant MELA-AU 17 1575962 1575962 single base substitution C T intron_variant MELA-AU 17 1576569 1576569 single base substitution C T downstream_gene_variant MELA-AU 17 1576569 1576569 single base substitution C T intron_variant MELA-AU 17 1576747 1576747 single base substitution G A downstream_gene_variant MELA-AU 17 1576747 1576747 single base substitution G A synonymous_variant F1187F 3561C>T MELA-AU 17 1576747 1576747 single base substitution G A upstream_gene_variant MELA-AU 17 1576902 1576902 single base substitution G A downstream_gene_variant MELA-AU 17 1576902 1576902 single base substitution G A intron_variant MELA-AU 17 1576902 1576902 single base substitution G A upstream_gene_variant MELA-AU 17 1577612 1577612 single base substitution G A downstream_gene_variant MELA-AU 17 1577612 1577612 single base substitution G A intron_variant MELA-AU 17 1577612 1577612 single base substitution G A upstream_gene_variant MELA-AU 17 1577842 1577842 single base substitution G A downstream_gene_variant MELA-AU 17 1577842 1577842 single base substitution G A missense_variant P1010S 3028C>T MELA-AU 17 1577842 1577842 single base substitution G A missense_variant P1065S 3193C>T MELA-AU 17 1577842 1577842 single base substitution G A upstream_gene_variant MELA-AU 17 1578097 1578097 single base substitution C T downstream_gene_variant MELA-AU 17 1578097 1578097 single base substitution C T intron_variant MELA-AU 17 1578097 1578097 single base substitution C T upstream_gene_variant MELA-AU 17 1578261 1578261 single base substitution G A downstream_gene_variant MELA-AU 17 1578261 1578261 single base substitution G A intron_variant MELA-AU 17 1578261 1578261 single base substitution G A upstream_gene_variant MELA-AU 17 1578895 1578895 single base substitution G A downstream_gene_variant MELA-AU 17 1578895 1578895 single base substitution G A intron_variant MELA-AU 17 1578895 1578895 single base substitution G A upstream_gene_variant MELA-AU 17 1579439 1579439 single base substitution G A downstream_gene_variant MELA-AU 17 1579439 1579439 single base substitution G A intron_variant MELA-AU 17 1579439 1579439 single base substitution G A upstream_gene_variant MELA-AU 17 1580250 1580251 multiple base substitution (>=2bp and <=200bp) GG TA downstream_gene_variant MELA-AU 17 1580250 1580251 multiple base substitution (>=2bp and <=200bp) GG TA intron_variant MELA-AU 17 1580250 1580251 multiple base substitution (>=2bp and <=200bp) GG TA upstream_gene_variant MELA-AU 17 1581823 1581823 single base substitution G A downstream_gene_variant MELA-AU 17 1581823 1581823 single base substitution G A exon_variant MELA-AU 17 1581823 1581823 single base substitution G A missense_variant R560C 1678C>T MELA-AU 17 1581823 1581823 single base substitution G A missense_variant R615C 1843C>T MELA-AU 17 1581823 1581823 single base substitution G A upstream_gene_variant MELA-AU 17 1581892 1581892 single base substitution A G downstream_gene_variant MELA-AU 17 1581892 1581892 single base substitution A G exon_variant MELA-AU 17 1581892 1581892 single base substitution A G missense_variant Y537H 1609T>C MELA-AU 17 1581892 1581892 single base substitution A G missense_variant Y592H 1774T>C MELA-AU 17 1581892 1581892 single base substitution A G upstream_gene_variant MELA-AU 17 1581947 1581947 single base substitution C T downstream_gene_variant MELA-AU 17 1581947 1581947 single base substitution C T splice_acceptor_variant MELA-AU 17 1581947 1581947 single base substitution C T upstream_gene_variant MELA-AU 17 1582485 1582486 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 17 1582485 1582486 multiple base substitution (>=2bp and <=200bp) GG AA exon_variant MELA-AU 17 1582485 1582486 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant S420F 1259CC>TT MELA-AU 17 1582485 1582486 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant S475F 1424CC>TT MELA-AU 17 1582485 1582486 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 17 1582516 1582516 single base substitution G A downstream_gene_variant MELA-AU 17 1582516 1582516 single base substitution G A intron_variant MELA-AU 17 1582516 1582516 single base substitution G A upstream_gene_variant MELA-AU 17 1582657 1582657 single base substitution G A downstream_gene_variant MELA-AU 17 1582657 1582657 single base substitution G A missense_variant S391F 1172C>T MELA-AU 17 1582657 1582657 single base substitution G A missense_variant S446F 1337C>T MELA-AU 17 1582657 1582657 single base substitution G A upstream_gene_variant MELA-AU 17 1582797 1582797 single base substitution G A downstream_gene_variant MELA-AU 17 1582797 1582797 single base substitution G A intron_variant MELA-AU 17 1582797 1582797 single base substitution G A upstream_gene_variant MELA-AU 17 1582934 1582934 single base substitution G A downstream_gene_variant MELA-AU 17 1582934 1582934 single base substitution G A missense_variant R365W 1093C>T MELA-AU 17 1582934 1582934 single base substitution G A missense_variant R420W 1258C>T MELA-AU 17 1582934 1582934 single base substitution G A upstream_gene_variant MELA-AU 17 1583286 1583286 single base substitution G A downstream_gene_variant MELA-AU 17 1583286 1583286 single base substitution G A intron_variant MELA-AU 17 1583286 1583286 single base substitution G A upstream_gene_variant MELA-AU 17 1584422 1584422 single base substitution G A downstream_gene_variant MELA-AU 17 1584422 1584422 single base substitution G A intron_variant MELA-AU 17 1584422 1584422 single base substitution G A upstream_gene_variant MELA-AU 17 1586481 1586481 single base substitution G A exon_variant MELA-AU 17 1586481 1586481 single base substitution G A intron_variant MELA-AU 17 1586481 1586481 single base substitution G A upstream_gene_variant MELA-AU 17 1586781 1586781 single base substitution G A exon_variant MELA-AU 17 1586781 1586781 single base substitution G A intron_variant MELA-AU 17 1586781 1586781 single base substitution G A upstream_gene_variant MELA-AU 17 1588078 1588078 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 17 1588078 1588078 single base substitution C T exon_variant MELA-AU 17 1588078 1588078 single base substitution C T upstream_gene_variant MELA-AU 17 1588209 1588209 single base substitution G A upstream_gene_variant MELA-AU 17 1588251 1588251 single base substitution G A upstream_gene_variant MELA-AU 17 1588254 1588254 single base substitution G A upstream_gene_variant MELA-AU 17 1588272 1588272 single base substitution G A upstream_gene_variant MELA-AU 17 1588275 1588276 multiple base substitution (>=2bp and <=200bp) AG GA upstream_gene_variant MELA-AU 17 1588276 1588276 single base substitution G A upstream_gene_variant MELA-AU 17 1588323 1588323 single base substitution C T upstream_gene_variant MELA-AU 17 1588788 1588788 single base substitution C T upstream_gene_variant MELA-AU 17 1591163 1591163 single base substitution G C upstream_gene_variant MELA-AU 17 1591271 1591271 single base substitution G A upstream_gene_variant MELA-AU 17 1591478 1591478 single base substitution C T upstream_gene_variant MELA-AU 17 1591717 1591717 single base substitution C T upstream_gene_variant MELA-AU 17 1592497 1592497 single base substitution G A upstream_gene_variant ORCA-IN 17 1550281 1550281 single base substitution T C downstream_gene_variant ORCA-IN 17 1554213 1554213 single base substitution C A downstream_gene_variant ORCA-IN 17 1554213 1554213 single base substitution C A exon_variant ORCA-IN 17 1554213 1554213 single base substitution C A intron_variant ORCA-IN 17 1554213 1554213 single base substitution C A missense_variant Q2297H 6891G>T ORCA-IN 17 1569475 1569475 single base substitution G C intron_variant ORCA-IN 17 1569475 1569475 single base substitution G C upstream_gene_variant ORCA-IN 17 1577915 1577915 single base substitution G T downstream_gene_variant ORCA-IN 17 1577915 1577915 single base substitution G T synonymous_variant I1040I 3120C>A ORCA-IN 17 1577915 1577915 single base substitution G T synonymous_variant I985I 2955C>A ORCA-IN 17 1577915 1577915 single base substitution G T upstream_gene_variant OV-AU 17 1556534 1556534 single base substitution G A exon_variant OV-AU 17 1556534 1556534 single base substitution G A intron_variant OV-AU 17 1556534 1556534 single base substitution G A upstream_gene_variant OV-AU 17 1559185 1559185 single base substitution C T downstream_gene_variant OV-AU 17 1559185 1559185 single base substitution C T intron_variant OV-AU 17 1559185 1559185 single base substitution C T upstream_gene_variant OV-AU 17 1560148 1560148 single base substitution C T downstream_gene_variant OV-AU 17 1560148 1560148 single base substitution C T intron_variant OV-AU 17 1560148 1560148 single base substitution C T upstream_gene_variant OV-AU 17 1568422 1568422 single base substitution C G intron_variant OV-AU 17 1568422 1568422 single base substitution C G upstream_gene_variant OV-AU 17 1572815 1572815 single base substitution T A downstream_gene_variant OV-AU 17 1572815 1572815 single base substitution T A intron_variant OV-US 17 1578513 1578513 single base substitution C G downstream_gene_variant OV-US 17 1578513 1578513 single base substitution C G exon_variant OV-US 17 1578513 1578513 single base substitution C G missense_variant R943P 2828G>C OV-US 17 1578513 1578513 single base substitution C G missense_variant R998P 2993G>C OV-US 17 1578513 1578513 single base substitution C G upstream_gene_variant PACA-AU 17 1550381 1550381 single base substitution G A downstream_gene_variant PACA-AU 17 1563077 1563077 single base substitution G A downstream_gene_variant PACA-AU 17 1563077 1563077 single base substitution G A exon_variant PACA-AU 17 1563077 1563077 single base substitution G A intron_variant PACA-AU 17 1563077 1563077 single base substitution G A upstream_gene_variant PACA-AU 17 1568093 1568093 single base substitution G C intron_variant PACA-AU 17 1568093 1568093 single base substitution G C upstream_gene_variant PACA-AU 17 1577440 1577440 single base substitution C T downstream_gene_variant PACA-AU 17 1577440 1577440 single base substitution C T intron_variant PACA-AU 17 1577440 1577440 single base substitution C T upstream_gene_variant PACA-AU 17 1581440 1581440 single base substitution C G downstream_gene_variant PACA-AU 17 1581440 1581440 single base substitution C G intron_variant PACA-AU 17 1581440 1581440 single base substitution C G upstream_gene_variant PACA-AU 17 1581878 1581878 single base substitution G A downstream_gene_variant PACA-AU 17 1581878 1581878 single base substitution G A exon_variant PACA-AU 17 1581878 1581878 single base substitution G A synonymous_variant Y541Y 1623C>T PACA-AU 17 1581878 1581878 single base substitution G A synonymous_variant Y596Y 1788C>T PACA-AU 17 1581878 1581878 single base substitution G A upstream_gene_variant PACA-AU 17 1582561 1582561 single base substitution C T downstream_gene_variant PACA-AU 17 1582561 1582561 single base substitution C T intron_variant PACA-AU 17 1582561 1582561 single base substitution C T upstream_gene_variant PACA-AU 17 1591224 1591224 single base substitution A T upstream_gene_variant PACA-AU 17 1591330 1591330 single base substitution G A upstream_gene_variant PACA-AU 17 1592782 1592782 single base substitution C T upstream_gene_variant PACA-AU 17 1592831 1592831 single base substitution T C upstream_gene_variant PACA-CA 17 1558730 1558730 single base substitution G A downstream_gene_variant PACA-CA 17 1558730 1558730 single base substitution G A synonymous_variant I1967I 5901C>T PACA-CA 17 1558730 1558730 single base substitution G A upstream_gene_variant PACA-CA 17 1560289 1560289 insertion of <=200bp - AC downstream_gene_variant PACA-CA 17 1560289 1560289 insertion of <=200bp - AC intron_variant PACA-CA 17 1560289 1560289 insertion of <=200bp - AC upstream_gene_variant PACA-CA 17 1567553 1567553 single base substitution C A intron_variant PACA-CA 17 1567553 1567553 single base substitution C A upstream_gene_variant PACA-CA 17 1570653 1570653 single base substitution T C intron_variant PACA-CA 17 1571858 1571858 single base substitution G A downstream_gene_variant PACA-CA 17 1571858 1571858 single base substitution G A intron_variant PACA-CA 17 1572091 1572091 single base substitution C T downstream_gene_variant PACA-CA 17 1572091 1572091 single base substitution C T intron_variant PACA-CA 17 1573901 1573901 single base substitution C T downstream_gene_variant PACA-CA 17 1573901 1573901 single base substitution C T intron_variant PACA-CA 17 1574463 1574463 single base substitution C T downstream_gene_variant PACA-CA 17 1574463 1574463 single base substitution C T intron_variant PACA-CA 17 1586578 1586578 single base substitution C T exon_variant PACA-CA 17 1586578 1586578 single base substitution C T intron_variant PACA-CA 17 1586578 1586578 single base substitution C T upstream_gene_variant PACA-CA 17 1588838 1588838 single base substitution A G upstream_gene_variant PAEN-AU 17 1577275 1577275 single base substitution A C downstream_gene_variant PAEN-AU 17 1577275 1577275 single base substitution A C intron_variant PAEN-AU 17 1577275 1577275 single base substitution A C upstream_gene_variant PAEN-IT 17 1564477 1564477 single base substitution G A exon_variant PAEN-IT 17 1564477 1564477 single base substitution G A intron_variant PAEN-IT 17 1566369 1566369 single base substitution G T intron_variant PAEN-IT 17 1566369 1566369 single base substitution G T upstream_gene_variant PAEN-IT 17 1587453 1587453 single base substitution T C intron_variant PAEN-IT 17 1587453 1587453 single base substitution T C upstream_gene_variant PBCA-DE 17 1550576 1550576 single base substitution G A downstream_gene_variant PBCA-DE 17 1557459 1557459 single base substitution C T exon_variant PBCA-DE 17 1557459 1557459 single base substitution C T intron_variant PBCA-DE 17 1557459 1557459 single base substitution C T upstream_gene_variant PBCA-DE 17 1557714 1557715 deletion of <=200bp GT - exon_variant PBCA-DE 17 1557714 1557715 deletion of <=200bp GT - intron_variant PBCA-DE 17 1557714 1557715 deletion of <=200bp GT - upstream_gene_variant PBCA-DE 17 1560667 1560668 deletion of <=200bp CG - downstream_gene_variant PBCA-DE 17 1560667 1560668 deletion of <=200bp CG - intron_variant PBCA-DE 17 1560667 1560668 deletion of <=200bp CG - upstream_gene_variant PBCA-DE 17 1562788 1562788 single base substitution G A downstream_gene_variant PBCA-DE 17 1562788 1562788 single base substitution G A exon_variant PBCA-DE 17 1562788 1562788 single base substitution G A synonymous_variant R1667R 5001C>T PBCA-DE 17 1562788 1562788 single base substitution G A upstream_gene_variant PBCA-DE 17 1562927 1562927 single base substitution C A downstream_gene_variant PBCA-DE 17 1562927 1562927 single base substitution C A exon_variant PBCA-DE 17 1562927 1562927 single base substitution C A intron_variant PBCA-DE 17 1562927 1562927 single base substitution C A upstream_gene_variant PBCA-DE 17 1569175 1569175 deletion of <=200bp C - intron_variant PBCA-DE 17 1569175 1569175 deletion of <=200bp C - upstream_gene_variant PBCA-DE 17 1574230 1574230 deletion of <=200bp A - downstream_gene_variant PBCA-DE 17 1574230 1574230 deletion of <=200bp A - intron_variant PBCA-DE 17 1578511 1578511 single base substitution G A downstream_gene_variant PBCA-DE 17 1578511 1578511 single base substitution G A exon_variant PBCA-DE 17 1578511 1578511 single base substitution G A missense_variant L944F 2830C>T PBCA-DE 17 1578511 1578511 single base substitution G A missense_variant L999F 2995C>T PBCA-DE 17 1578511 1578511 single base substitution G A upstream_gene_variant PBCA-DE 17 1580426 1580426 single base substitution C T downstream_gene_variant PBCA-DE 17 1580426 1580426 single base substitution C T exon_variant PBCA-DE 17 1580426 1580426 single base substitution C T synonymous_variant Q620Q 1860G>A PBCA-DE 17 1580426 1580426 single base substitution C T synonymous_variant Q675Q 2025G>A PBCA-DE 17 1580426 1580426 single base substitution C T upstream_gene_variant PBCA-DE 17 1592546 1592546 single base substitution A G upstream_gene_variant PBCA-DE 17 1592757 1592757 deletion of <=200bp C - upstream_gene_variant PBCA-DE 17 1593132 1593132 insertion of <=200bp - CC upstream_gene_variant PRAD-UK 17 1558086 1558086 single base substitution G A downstream_gene_variant PRAD-UK 17 1558086 1558086 single base substitution G A exon_variant PRAD-UK 17 1558086 1558086 single base substitution G A intron_variant PRAD-UK 17 1558086 1558086 single base substitution G A upstream_gene_variant PRAD-UK 17 1568535 1568538 deletion of <=200bp AGAA - intron_variant PRAD-UK 17 1568535 1568538 deletion of <=200bp AGAA - upstream_gene_variant PRAD-UK 17 1583652 1583652 single base substitution G C downstream_gene_variant PRAD-UK 17 1583652 1583652 single base substitution G C intron_variant PRAD-UK 17 1583652 1583652 single base substitution G C upstream_gene_variant PRAD-UK 17 1592094 1592094 single base substitution G A upstream_gene_variant PRAD-UK 17 1592385 1592385 single base substitution C T upstream_gene_variant PRAD-US 17 1559946 1559946 single base substitution A C downstream_gene_variant PRAD-US 17 1559946 1559946 single base substitution A C missense_variant L1872R 5615T>G PRAD-US 17 1559946 1559946 single base substitution A C upstream_gene_variant PRAD-US 17 1560049 1560049 single base substitution T C downstream_gene_variant PRAD-US 17 1560049 1560049 single base substitution T C missense_variant K1838E 5512A>G PRAD-US 17 1560049 1560049 single base substitution T C upstream_gene_variant PRAD-US 17 1563822 1563822 single base substitution G A downstream_gene_variant PRAD-US 17 1563822 1563822 single base substitution G A exon_variant PRAD-US 17 1563822 1563822 single base substitution G A synonymous_variant H1563H 4689C>T PRAD-US 17 1563822 1563822 single base substitution G A synonymous_variant H206H 618C>T READ-US 17 1548956 1548956 insertion of <=200bp - AGC downstream_gene_variant READ-US 17 1577960 1577960 single base substitution C T downstream_gene_variant READ-US 17 1577960 1577960 single base substitution C T exon_variant READ-US 17 1577960 1577960 single base substitution C T synonymous_variant T1025T 3075G>A READ-US 17 1577960 1577960 single base substitution C T synonymous_variant T970T 2910G>A READ-US 17 1577960 1577960 single base substitution C T upstream_gene_variant RECA-EU 17 1571655 1571655 single base substitution T G downstream_gene_variant RECA-EU 17 1571655 1571655 single base substitution T G intron_variant RECA-EU 17 1572246 1572246 single base substitution G C downstream_gene_variant RECA-EU 17 1572246 1572246 single base substitution G C intron_variant RECA-EU 17 1583268 1583268 single base substitution G A downstream_gene_variant RECA-EU 17 1583268 1583268 single base substitution G A intron_variant RECA-EU 17 1583268 1583268 single base substitution G A upstream_gene_variant RECA-EU 17 1583966 1583966 single base substitution C G downstream_gene_variant RECA-EU 17 1583966 1583966 single base substitution C G exon_variant RECA-EU 17 1583966 1583966 single base substitution C G intron_variant RECA-EU 17 1583966 1583966 single base substitution C G upstream_gene_variant RECA-EU 17 1584004 1584004 single base substitution C G downstream_gene_variant RECA-EU 17 1584004 1584004 single base substitution C G exon_variant RECA-EU 17 1584004 1584004 single base substitution C G intron_variant RECA-EU 17 1584004 1584004 single base substitution C G upstream_gene_variant RECA-EU 17 1589443 1589443 single base substitution G A upstream_gene_variant SKCA-BR 17 1552650 1552650 single base substitution A G downstream_gene_variant SKCA-BR 17 1552682 1552682 single base substitution T C downstream_gene_variant SKCA-BR 17 1553123 1553123 single base substitution A C downstream_gene_variant SKCA-BR 17 1553634 1553634 single base substitution A G downstream_gene_variant SKCA-BR 17 1553896 1553896 single base substitution A G downstream_gene_variant SKCA-BR 17 1559016 1559016 single base substitution G A downstream_gene_variant SKCA-BR 17 1559016 1559016 single base substitution G A intron_variant SKCA-BR 17 1559016 1559016 single base substitution G A upstream_gene_variant SKCA-BR 17 1559347 1559348 deletion of <=200bp TG - downstream_gene_variant SKCA-BR 17 1559347 1559348 deletion of <=200bp TG - intron_variant SKCA-BR 17 1559347 1559348 deletion of <=200bp TG - upstream_gene_variant SKCA-BR 17 1559900 1559900 single base substitution G A downstream_gene_variant SKCA-BR 17 1559900 1559900 single base substitution G A intron_variant SKCA-BR 17 1559900 1559900 single base substitution G A upstream_gene_variant SKCA-BR 17 1561266 1561266 single base substitution A C downstream_gene_variant SKCA-BR 17 1561266 1561266 single base substitution A C intron_variant SKCA-BR 17 1561266 1561266 single base substitution A C upstream_gene_variant SKCA-BR 17 1565501 1565501 single base substitution T G intron_variant SKCA-BR 17 1565501 1565501 single base substitution T G upstream_gene_variant SKCA-BR 17 1569139 1569139 insertion of <=200bp - CA intron_variant SKCA-BR 17 1569139 1569139 insertion of <=200bp - CA upstream_gene_variant SKCA-BR 17 1570404 1570404 single base substitution T G intron_variant SKCA-BR 17 1570832 1570833 deletion of <=200bp CT - intron_variant SKCA-BR 17 1571655 1571655 single base substitution T G downstream_gene_variant SKCA-BR 17 1571655 1571655 single base substitution T G intron_variant SKCA-BR 17 1572030 1572030 single base substitution C T downstream_gene_variant SKCA-BR 17 1572030 1572030 single base substitution C T intron_variant SKCA-BR 17 1573801 1573801 single base substitution A T downstream_gene_variant SKCA-BR 17 1573801 1573801 single base substitution A T intron_variant SKCA-BR 17 1575190 1575190 single base substitution G C downstream_gene_variant SKCA-BR 17 1575190 1575190 single base substitution G C intron_variant SKCA-BR 17 1576524 1576524 single base substitution G A downstream_gene_variant SKCA-BR 17 1576524 1576524 single base substitution G A intron_variant SKCA-BR 17 1577750 1577750 single base substitution G A downstream_gene_variant SKCA-BR 17 1577750 1577750 single base substitution G A synonymous_variant I1095I 3285C>T SKCA-BR 17 1577750 1577750 single base substitution G A upstream_gene_variant SKCA-BR 17 1578835 1578835 single base substitution A G downstream_gene_variant SKCA-BR 17 1578835 1578835 single base substitution A G intron_variant SKCA-BR 17 1578835 1578835 single base substitution A G upstream_gene_variant SKCA-BR 17 1586402 1586402 single base substitution G A exon_variant SKCA-BR 17 1586402 1586402 single base substitution G A intron_variant SKCA-BR 17 1586402 1586402 single base substitution G A upstream_gene_variant SKCA-BR 17 1587182 1587183 deletion of <=200bp CT - intron_variant SKCA-BR 17 1587182 1587183 deletion of <=200bp CT - upstream_gene_variant SKCA-BR 17 1588276 1588276 single base substitution G A upstream_gene_variant SKCA-BR 17 1588282 1588282 single base substitution G A upstream_gene_variant SKCA-BR 17 1588907 1588907 single base substitution G A upstream_gene_variant SKCA-BR 17 1589802 1589802 single base substitution G A upstream_gene_variant SKCA-BR 17 1590931 1590931 single base substitution G A upstream_gene_variant SKCA-BR 17 1590932 1590932 single base substitution G A upstream_gene_variant SKCA-BR 17 1592316 1592316 single base substitution A C upstream_gene_variant SKCA-BR 17 1592546 1592546 single base substitution A G upstream_gene_variant SKCA-BR 17 1592602 1592602 single base substitution T C upstream_gene_variant SKCA-BR 17 1593139 1593139 single base substitution A C upstream_gene_variant SKCM-US 17 1548956 1548956 insertion of <=200bp - AGC downstream_gene_variant SKCM-US 17 1549852 1549852 single base substitution G A downstream_gene_variant SKCM-US 17 1549859 1549859 single base substitution G A downstream_gene_variant SKCM-US 17 1551726 1551726 single base substitution C T downstream_gene_variant SKCM-US 17 1552937 1552937 single base substitution C T downstream_gene_variant SKCM-US 17 1555054 1555054 single base substitution G A downstream_gene_variant SKCM-US 17 1555054 1555054 single base substitution G A exon_variant SKCM-US 17 1555054 1555054 single base substitution G A missense_variant P2133L 6398C>T SKCM-US 17 1555054 1555054 single base substitution G A upstream_gene_variant SKCM-US 17 1558786 1558786 single base substitution G A downstream_gene_variant SKCM-US 17 1558786 1558786 single base substitution G A missense_variant R1949W 5845C>T SKCM-US 17 1558786 1558786 single base substitution G A upstream_gene_variant SKCM-US 17 1558805 1558805 single base substitution G A downstream_gene_variant SKCM-US 17 1558805 1558805 single base substitution G A synonymous_variant A1942A 5826C>T SKCM-US 17 1558805 1558805 single base substitution G A upstream_gene_variant SKCM-US 17 1559773 1559773 single base substitution G A downstream_gene_variant SKCM-US 17 1559773 1559773 single base substitution G A synonymous_variant F1902F 5706C>T SKCM-US 17 1559773 1559773 single base substitution G A upstream_gene_variant SKCM-US 17 1559958 1559958 single base substitution A C downstream_gene_variant SKCM-US 17 1559958 1559958 single base substitution A C missense_variant M1868R 5603T>G SKCM-US 17 1559958 1559958 single base substitution A C upstream_gene_variant SKCM-US 17 1562025 1562025 single base substitution G A downstream_gene_variant SKCM-US 17 1562025 1562025 single base substitution G A missense_variant P1724L 5171C>T SKCM-US 17 1562025 1562025 single base substitution G A upstream_gene_variant SKCM-US 17 1562737 1562737 single base substitution G A downstream_gene_variant SKCM-US 17 1562737 1562737 single base substitution G A synonymous_variant F1684F 5052C>T SKCM-US 17 1562737 1562737 single base substitution G A upstream_gene_variant SKCM-US 17 1563247 1563247 single base substitution C T downstream_gene_variant SKCM-US 17 1563247 1563247 single base substitution C T exon_variant SKCM-US 17 1563247 1563247 single base substitution C T missense_variant E1612K 4834G>A SKCM-US 17 1563247 1563247 single base substitution C T upstream_gene_variant SKCM-US 17 1563755 1563755 single base substitution G A downstream_gene_variant SKCM-US 17 1563755 1563755 single base substitution G A exon_variant SKCM-US 17 1563755 1563755 single base substitution G A missense_variant H1586Y 4756C>T SKCM-US 17 1563755 1563755 single base substitution G A missense_variant H229Y 685C>T SKCM-US 17 1564010 1564010 single base substitution C A downstream_gene_variant SKCM-US 17 1564010 1564010 single base substitution C A exon_variant SKCM-US 17 1564010 1564010 single base substitution C A synonymous_variant P1540P 4620G>T SKCM-US 17 1564010 1564010 single base substitution C A synonymous_variant P183P 549G>T SKCM-US 17 1564924 1564924 single base substitution C T exon_variant SKCM-US 17 1564924 1564924 single base substitution C T intron_variant SKCM-US 17 1564924 1564924 single base substitution C T missense_variant E1395K 4183G>A SKCM-US 17 1564924 1564924 single base substitution C T upstream_gene_variant SKCM-US 17 1577111 1577111 single base substitution G A downstream_gene_variant SKCM-US 17 1577111 1577111 single base substitution G A synonymous_variant I1125I 3375C>T SKCM-US 17 1577111 1577111 single base substitution G A upstream_gene_variant SKCM-US 17 1577738 1577738 single base substitution G A downstream_gene_variant SKCM-US 17 1577738 1577738 single base substitution G A splice_region_variant SKCM-US 17 1577738 1577738 single base substitution G A upstream_gene_variant SKCM-US 17 1577966 1577966 single base substitution G A downstream_gene_variant SKCM-US 17 1577966 1577966 single base substitution G A exon_variant SKCM-US 17 1577966 1577966 single base substitution G A synonymous_variant N1023N 3069C>T SKCM-US 17 1577966 1577966 single base substitution G A synonymous_variant N968N 2904C>T SKCM-US 17 1577966 1577966 single base substitution G A upstream_gene_variant SKCM-US 17 1579318 1579318 single base substitution C T downstream_gene_variant SKCM-US 17 1579318 1579318 single base substitution C T synonymous_variant R806R 2418G>A SKCM-US 17 1579318 1579318 single base substitution C T synonymous_variant R861R 2583G>A SKCM-US 17 1579318 1579318 single base substitution C T upstream_gene_variant SKCM-US 17 1579541 1579541 single base substitution A G downstream_gene_variant SKCM-US 17 1579541 1579541 single base substitution A G synonymous_variant L783L 2347T>C SKCM-US 17 1579541 1579541 single base substitution A G synonymous_variant L838L 2512T>C SKCM-US 17 1579541 1579541 single base substitution A G upstream_gene_variant SKCM-US 17 1579804 1579804 single base substitution G A downstream_gene_variant SKCM-US 17 1579804 1579804 single base substitution G A exon_variant SKCM-US 17 1579804 1579804 single base substitution G A synonymous_variant L740L 2218C>T SKCM-US 17 1579804 1579804 single base substitution G A synonymous_variant L795L 2383C>T SKCM-US 17 1579804 1579804 single base substitution G A upstream_gene_variant SKCM-US 17 1580001 1580001 single base substitution G A downstream_gene_variant SKCM-US 17 1580001 1580001 single base substitution G A exon_variant SKCM-US 17 1580001 1580001 single base substitution G A missense_variant P674L 2021C>T SKCM-US 17 1580001 1580001 single base substitution G A missense_variant P729L 2186C>T SKCM-US 17 1580001 1580001 single base substitution G A upstream_gene_variant SKCM-US 17 1581861 1581861 single base substitution A C downstream_gene_variant SKCM-US 17 1581861 1581861 single base substitution A C exon_variant SKCM-US 17 1581861 1581861 single base substitution A C missense_variant I547S 1640T>G SKCM-US 17 1581861 1581861 single base substitution A C missense_variant I602S 1805T>G SKCM-US 17 1581861 1581861 single base substitution A C upstream_gene_variant SKCM-US 17 1581892 1581892 single base substitution A G downstream_gene_variant SKCM-US 17 1581892 1581892 single base substitution A G exon_variant SKCM-US 17 1581892 1581892 single base substitution A G missense_variant Y537H 1609T>C SKCM-US 17 1581892 1581892 single base substitution A G missense_variant Y592H 1774T>C SKCM-US 17 1581892 1581892 single base substitution A G upstream_gene_variant SKCM-US 17 1582092 1582092 single base substitution G A downstream_gene_variant SKCM-US 17 1582092 1582092 single base substitution G A exon_variant SKCM-US 17 1582092 1582092 single base substitution G A synonymous_variant H506H 1518C>T SKCM-US 17 1582092 1582092 single base substitution G A synonymous_variant H561H 1683C>T SKCM-US 17 1582092 1582092 single base substitution G A upstream_gene_variant SKCM-US 17 1582486 1582486 single base substitution G A downstream_gene_variant SKCM-US 17 1582486 1582486 single base substitution G A exon_variant SKCM-US 17 1582486 1582486 single base substitution G A missense_variant S420F 1259C>T SKCM-US 17 1582486 1582486 single base substitution G A missense_variant S475F 1424C>T SKCM-US 17 1582486 1582486 single base substitution G A upstream_gene_variant SKCM-US 17 1584067 1584067 single base substitution A T downstream_gene_variant SKCM-US 17 1584067 1584067 single base substitution A T exon_variant SKCM-US 17 1584067 1584067 single base substitution A T missense_variant Y296N 886T>A SKCM-US 17 1584067 1584067 single base substitution A T missense_variant Y351N 1051T>A SKCM-US 17 1584067 1584067 single base substitution A T upstream_gene_variant SKCM-US 17 1584244 1584244 single base substitution G A downstream_gene_variant SKCM-US 17 1584244 1584244 single base substitution G A exon_variant SKCM-US 17 1584244 1584244 single base substitution G A missense_variant P269L 806C>T SKCM-US 17 1584244 1584244 single base substitution G A missense_variant P324L 971C>T SKCM-US 17 1584244 1584244 single base substitution G A upstream_gene_variant SKCM-US 17 1585293 1585293 single base substitution C T downstream_gene_variant SKCM-US 17 1585293 1585293 single base substitution C T synonymous_variant R103R 309G>A SKCM-US 17 1585293 1585293 single base substitution C T synonymous_variant R158R 474G>A SKCM-US 17 1585293 1585293 single base substitution C T upstream_gene_variant SKCM-US 17 1585460 1585460 single base substitution G A downstream_gene_variant SKCM-US 17 1585460 1585460 single base substitution G A intron_variant SKCM-US 17 1585460 1585460 single base substitution G A missense_variant P133S 397C>T SKCM-US 17 1585460 1585460 single base substitution G A upstream_gene_variant SKCM-US 17 1585565 1585565 single base substitution C T downstream_gene_variant SKCM-US 17 1585565 1585565 single base substitution C T intron_variant SKCM-US 17 1585565 1585565 single base substitution C T missense_variant A98T 292G>A SKCM-US 17 1585565 1585565 single base substitution C T upstream_gene_variant SKCM-US 17 1586852 1586852 single base substitution G T exon_variant SKCM-US 17 1586852 1586852 single base substitution G T missense_variant R82S 244C>A SKCM-US 17 1586852 1586852 single base substitution G T upstream_gene_variant SKCM-US 17 1587789 1587789 single base substitution G A exon_variant SKCM-US 17 1587789 1587789 single base substitution G A missense_variant S26L 77C>T SKCM-US 17 1587789 1587789 single base substitution G A upstream_gene_variant STAD-US 17 1549887 1549887 single base substitution G T downstream_gene_variant STAD-US 17 1552944 1552944 single base substitution G A downstream_gene_variant STAD-US 17 1559716 1559716 single base substitution G A downstream_gene_variant STAD-US 17 1559716 1559716 single base substitution G A synonymous_variant D1921D 5763C>T STAD-US 17 1559716 1559716 single base substitution G A upstream_gene_variant STAD-US 17 1559814 1559814 single base substitution G A downstream_gene_variant STAD-US 17 1559814 1559814 single base substitution G A missense_variant L1889F 5665C>T STAD-US 17 1559814 1559814 single base substitution G A upstream_gene_variant STAD-US 17 1562781 1562781 deletion of <=200bp C - downstream_gene_variant STAD-US 17 1562781 1562781 deletion of <=200bp C - exon_variant STAD-US 17 1562781 1562781 deletion of <=200bp C - frameshift_variant D1670 STAD-US 17 1562781 1562781 deletion of <=200bp C - upstream_gene_variant STAD-US 17 1562830 1562830 single base substitution G A downstream_gene_variant STAD-US 17 1562830 1562830 single base substitution G A exon_variant STAD-US 17 1562830 1562830 single base substitution G A synonymous_variant D1653D 4959C>T STAD-US 17 1562830 1562830 single base substitution G A upstream_gene_variant STAD-US 17 1565203 1565203 single base substitution A C missense_variant L1340R 4019T>G STAD-US 17 1565203 1565203 single base substitution A C missense_variant L43R 128T>G STAD-US 17 1565203 1565203 single base substitution A C upstream_gene_variant STAD-US 17 1576438 1576438 single base substitution C T downstream_gene_variant STAD-US 17 1576438 1576438 single base substitution C T exon_variant STAD-US 17 1576438 1576438 single base substitution C T missense_variant M1237I 3711G>A STAD-US 17 1576732 1576732 single base substitution G A downstream_gene_variant STAD-US 17 1576732 1576732 single base substitution G A synonymous_variant F1192F 3576C>T STAD-US 17 1576732 1576732 single base substitution G A upstream_gene_variant STAD-US 17 1577953 1577953 single base substitution A T downstream_gene_variant STAD-US 17 1577953 1577953 single base substitution A T exon_variant STAD-US 17 1577953 1577953 single base substitution A T missense_variant Y1028N 3082T>A STAD-US 17 1577953 1577953 single base substitution A T missense_variant Y973N 2917T>A STAD-US 17 1577953 1577953 single base substitution A T upstream_gene_variant STAD-US 17 1579329 1579329 single base substitution G A downstream_gene_variant STAD-US 17 1579329 1579329 single base substitution G A stop_gained Q803* 2407C>T STAD-US 17 1579329 1579329 single base substitution G A stop_gained Q858* 2572C>T STAD-US 17 1579329 1579329 single base substitution G A upstream_gene_variant STAD-US 17 1579343 1579343 single base substitution T C downstream_gene_variant STAD-US 17 1579343 1579343 single base substitution T C missense_variant K798R 2393A>G STAD-US 17 1579343 1579343 single base substitution T C missense_variant K853R 2558A>G STAD-US 17 1579343 1579343 single base substitution T C upstream_gene_variant STAD-US 17 1579520 1579520 single base substitution G A downstream_gene_variant STAD-US 17 1579520 1579520 single base substitution G A missense_variant R790W 2368C>T STAD-US 17 1579520 1579520 single base substitution G A missense_variant R845W 2533C>T STAD-US 17 1579520 1579520 single base substitution G A upstream_gene_variant STAD-US 17 1579567 1579567 deletion of <=200bp G - downstream_gene_variant STAD-US 17 1579567 1579567 deletion of <=200bp G - frameshift_variant P774 STAD-US 17 1579567 1579567 deletion of <=200bp G - frameshift_variant P829 STAD-US 17 1579567 1579567 deletion of <=200bp G - upstream_gene_variant STAD-US 17 1579927 1579927 single base substitution C T downstream_gene_variant STAD-US 17 1579927 1579927 single base substitution C T exon_variant STAD-US 17 1579927 1579927 single base substitution C T missense_variant A699T 2095G>A STAD-US 17 1579927 1579927 single base substitution C T missense_variant A754T 2260G>A STAD-US 17 1579927 1579927 single base substitution C T upstream_gene_variant STAD-US 17 1580395 1580395 single base substitution G A downstream_gene_variant STAD-US 17 1580395 1580395 single base substitution G A exon_variant STAD-US 17 1580395 1580395 single base substitution G A missense_variant R631W 1891C>T STAD-US 17 1580395 1580395 single base substitution G A missense_variant R686W 2056C>T STAD-US 17 1580395 1580395 single base substitution G A upstream_gene_variant STAD-US 17 1581900 1581900 single base substitution G A downstream_gene_variant STAD-US 17 1581900 1581900 single base substitution G A exon_variant STAD-US 17 1581900 1581900 single base substitution G A missense_variant T534M 1601C>T STAD-US 17 1581900 1581900 single base substitution G A missense_variant T589M 1766C>T STAD-US 17 1581900 1581900 single base substitution G A upstream_gene_variant STAD-US 17 1582418 1582418 single base substitution G A downstream_gene_variant STAD-US 17 1582418 1582418 single base substitution G A exon_variant STAD-US 17 1582418 1582418 single base substitution G A missense_variant R443C 1327C>T STAD-US 17 1582418 1582418 single base substitution G A missense_variant R498C 1492C>T STAD-US 17 1582418 1582418 single base substitution G A upstream_gene_variant STAD-US 17 1584919 1584919 single base substitution C T downstream_gene_variant STAD-US 17 1584919 1584919 single base substitution C T missense_variant R185H 554G>A STAD-US 17 1584919 1584919 single base substitution C T missense_variant R240H 719G>A STAD-US 17 1584919 1584919 single base substitution C T upstream_gene_variant STAD-US 17 1585245 1585245 single base substitution C T downstream_gene_variant STAD-US 17 1585245 1585245 single base substitution C T synonymous_variant P119P 357G>A STAD-US 17 1585245 1585245 single base substitution C T synonymous_variant P174P 522G>A STAD-US 17 1585245 1585245 single base substitution C T upstream_gene_variant STAD-US 17 1586851 1586851 single base substitution C T exon_variant STAD-US 17 1586851 1586851 single base substitution C T missense_variant R82H 245G>A STAD-US 17 1586851 1586851 single base substitution C T upstream_gene_variant STAD-US 17 1587865 1587865 single base substitution T C exon_variant STAD-US 17 1587865 1587865 single base substitution T C start_lost M1V 1A>G STAD-US 17 1587865 1587865 single base substitution T C upstream_gene_variant THCA-SA 17 1576486 1576486 deletion of <=200bp A - downstream_gene_variant THCA-SA 17 1576486 1576486 deletion of <=200bp A - exon_variant THCA-SA 17 1576486 1576486 deletion of <=200bp A - frameshift_variant T1221 THCA-US 17 1564570 1564570 single base substitution A C exon_variant THCA-US 17 1564570 1564570 single base substitution A C missense_variant Y1445D 4333T>G THCA-US 17 1564570 1564570 single base substitution A C missense_variant Y88D 262T>G THCA-US 17 1579616 1579616 single base substitution T C downstream_gene_variant THCA-US 17 1579616 1579616 single base substitution T C exon_variant THCA-US 17 1579616 1579616 single base substitution T C missense_variant T758A 2272A>G THCA-US 17 1579616 1579616 single base substitution T C missense_variant T813A 2437A>G THCA-US 17 1579616 1579616 single base substitution T C upstream_gene_variant UCEC-US 17 1549777 1549777 single base substitution C A downstream_gene_variant UCEC-US 17 1550250 1550250 single base substitution G A downstream_gene_variant UCEC-US 17 1550269 1550269 single base substitution C T downstream_gene_variant UCEC-US 17 1554107 1554107 single base substitution G A downstream_gene_variant UCEC-US 17 1554107 1554107 single base substitution G A missense_variant P65L 194C>T UCEC-US 17 1554107 1554107 single base substitution G A synonymous_variant L2333L 6997C>T UCEC-US 17 1554502 1554502 single base substitution G A downstream_gene_variant UCEC-US 17 1554502 1554502 single base substitution G A exon_variant UCEC-US 17 1554502 1554502 single base substitution G A synonymous_variant Y20Y 60C>T UCEC-US 17 1554502 1554502 single base substitution G A synonymous_variant Y2251Y 6753C>T UCEC-US 17 1554824 1554824 single base substitution G T downstream_gene_variant UCEC-US 17 1554824 1554824 single base substitution G T exon_variant UCEC-US 17 1554824 1554824 single base substitution G T synonymous_variant I2178I 6534C>A UCEC-US 17 1554824 1554824 single base substitution G T upstream_gene_variant UCEC-US 17 1555073 1555073 single base substitution A T downstream_gene_variant UCEC-US 17 1555073 1555073 single base substitution A T exon_variant UCEC-US 17 1555073 1555073 single base substitution A T missense_variant Y2127N 6379T>A UCEC-US 17 1555073 1555073 single base substitution A T upstream_gene_variant UCEC-US 17 1557144 1557144 single base substitution C T exon_variant UCEC-US 17 1557144 1557144 single base substitution C T missense_variant D2052N 6154G>A UCEC-US 17 1557144 1557144 single base substitution C T upstream_gene_variant UCEC-US 17 1557250 1557250 single base substitution G A exon_variant UCEC-US 17 1557250 1557250 single base substitution G A synonymous_variant I2016I 6048C>T UCEC-US 17 1557250 1557250 single base substitution G A upstream_gene_variant UCEC-US 17 1557250 1557250 single base substitution G T exon_variant UCEC-US 17 1557250 1557250 single base substitution G T synonymous_variant I2016I 6048C>A UCEC-US 17 1557250 1557250 single base substitution G T upstream_gene_variant UCEC-US 17 1559852 1559854 deletion of <=200bp AAG - disruptive_inframe_deletion HL1875Q UCEC-US 17 1559852 1559854 deletion of <=200bp AAG - downstream_gene_variant UCEC-US 17 1559852 1559854 deletion of <=200bp AAG - upstream_gene_variant UCEC-US 17 1559855 1559855 single base substitution T C downstream_gene_variant UCEC-US 17 1559855 1559855 single base substitution T C missense_variant H1875R 5624A>G UCEC-US 17 1559855 1559855 single base substitution T C upstream_gene_variant UCEC-US 17 1560022 1560022 single base substitution C T downstream_gene_variant UCEC-US 17 1560022 1560022 single base substitution C T missense_variant A1847T 5539G>A UCEC-US 17 1560022 1560022 single base substitution C T upstream_gene_variant UCEC-US 17 1561557 1561557 single base substitution C T downstream_gene_variant UCEC-US 17 1561557 1561557 single base substitution C T missense_variant R1832H 5495G>A UCEC-US 17 1561557 1561557 single base substitution C T upstream_gene_variant UCEC-US 17 1561558 1561558 single base substitution G A downstream_gene_variant UCEC-US 17 1561558 1561558 single base substitution G A missense_variant R1832C 5494C>T UCEC-US 17 1561558 1561558 single base substitution G A upstream_gene_variant UCEC-US 17 1561586 1561586 single base substitution G A downstream_gene_variant UCEC-US 17 1561586 1561586 single base substitution G A synonymous_variant I1822I 5466C>T UCEC-US 17 1561586 1561586 single base substitution G A upstream_gene_variant UCEC-US 17 1562031 1562031 single base substitution C T downstream_gene_variant UCEC-US 17 1562031 1562031 single base substitution C T missense_variant S1722N 5165G>A UCEC-US 17 1562031 1562031 single base substitution C T upstream_gene_variant UCEC-US 17 1563737 1563737 single base substitution C A downstream_gene_variant UCEC-US 17 1563737 1563737 single base substitution C A exon_variant UCEC-US 17 1563737 1563737 single base substitution C A missense_variant D1592Y 4774G>T UCEC-US 17 1563737 1563737 single base substitution C A missense_variant D235Y 703G>T UCEC-US 17 1564650 1564650 single base substitution C T exon_variant UCEC-US 17 1564650 1564650 single base substitution C T missense_variant R1418Q 4253G>A UCEC-US 17 1564650 1564650 single base substitution C T missense_variant R61Q 182G>A UCEC-US 17 1564650 1564650 single base substitution C T upstream_gene_variant UCEC-US 17 1564939 1564939 single base substitution C T exon_variant UCEC-US 17 1564939 1564939 single base substitution C T intron_variant UCEC-US 17 1564939 1564939 single base substitution C T missense_variant A1390T 4168G>A UCEC-US 17 1564939 1564939 single base substitution C T upstream_gene_variant UCEC-US 17 1565229 1565229 single base substitution G T synonymous_variant G1331G 3993C>A UCEC-US 17 1565229 1565229 single base substitution G T synonymous_variant G34G 102C>A UCEC-US 17 1565229 1565229 single base substitution G T upstream_gene_variant UCEC-US 17 1565373 1565373 single base substitution C T synonymous_variant E1283E 3849G>A UCEC-US 17 1565373 1565373 single base substitution C T upstream_gene_variant UCEC-US 17 1576786 1576786 single base substitution G A downstream_gene_variant UCEC-US 17 1576786 1576786 single base substitution G A synonymous_variant F1174F 3522C>T UCEC-US 17 1576786 1576786 single base substitution G A upstream_gene_variant UCEC-US 17 1577064 1577064 single base substitution C T downstream_gene_variant UCEC-US 17 1577064 1577064 single base substitution C T missense_variant R1141H 3422G>A UCEC-US 17 1577064 1577064 single base substitution C T upstream_gene_variant UCEC-US 17 1577887 1577887 single base substitution A G downstream_gene_variant UCEC-US 17 1577887 1577887 single base substitution A G synonymous_variant L1050L 3148T>C UCEC-US 17 1577887 1577887 single base substitution A G synonymous_variant L995L 2983T>C UCEC-US 17 1577887 1577887 single base substitution A G upstream_gene_variant UCEC-US 17 1577960 1577960 single base substitution C A downstream_gene_variant UCEC-US 17 1577960 1577960 single base substitution C A exon_variant UCEC-US 17 1577960 1577960 single base substitution C A synonymous_variant T1025T 3075G>T UCEC-US 17 1577960 1577960 single base substitution C A synonymous_variant T970T 2910G>T UCEC-US 17 1577960 1577960 single base substitution C A upstream_gene_variant UCEC-US 17 1578603 1578603 single base substitution G A downstream_gene_variant UCEC-US 17 1578603 1578603 single base substitution G A exon_variant UCEC-US 17 1578603 1578603 single base substitution G A missense_variant T913M 2738C>T UCEC-US 17 1578603 1578603 single base substitution G A missense_variant T968M 2903C>T UCEC-US 17 1578603 1578603 single base substitution G A upstream_gene_variant UCEC-US 17 1578988 1578988 single base substitution C T downstream_gene_variant UCEC-US 17 1578988 1578988 single base substitution C T missense_variant R878H 2633G>A UCEC-US 17 1578988 1578988 single base substitution C T missense_variant R933H 2798G>A UCEC-US 17 1578988 1578988 single base substitution C T upstream_gene_variant UCEC-US 17 1579034 1579034 single base substitution T A downstream_gene_variant UCEC-US 17 1579034 1579034 single base substitution T A missense_variant T863S 2587A>T UCEC-US 17 1579034 1579034 single base substitution T A missense_variant T918S 2752A>T UCEC-US 17 1579034 1579034 single base substitution T A upstream_gene_variant UCEC-US 17 1579577 1579577 single base substitution G T downstream_gene_variant UCEC-US 17 1579577 1579577 single base substitution G T missense_variant P771T 2311C>A UCEC-US 17 1579577 1579577 single base substitution G T missense_variant P826T 2476C>A UCEC-US 17 1579577 1579577 single base substitution G T upstream_gene_variant UCEC-US 17 1579594 1579594 single base substitution C T downstream_gene_variant UCEC-US 17 1579594 1579594 single base substitution C T missense_variant R765H 2294G>A UCEC-US 17 1579594 1579594 single base substitution C T missense_variant R820H 2459G>A UCEC-US 17 1579594 1579594 single base substitution C T upstream_gene_variant UCEC-US 17 1579845 1579845 single base substitution C T downstream_gene_variant UCEC-US 17 1579845 1579845 single base substitution C T exon_variant UCEC-US 17 1579845 1579845 single base substitution C T missense_variant R726Q 2177G>A UCEC-US 17 1579845 1579845 single base substitution C T missense_variant R781Q 2342G>A UCEC-US 17 1579845 1579845 single base substitution C T upstream_gene_variant UCEC-US 17 1581888 1581888 single base substitution C T downstream_gene_variant UCEC-US 17 1581888 1581888 single base substitution C T exon_variant UCEC-US 17 1581888 1581888 single base substitution C T missense_variant R538Q 1613G>A UCEC-US 17 1581888 1581888 single base substitution C T missense_variant R593Q 1778G>A UCEC-US 17 1581888 1581888 single base substitution C T upstream_gene_variant UCEC-US 17 1582133 1582133 single base substitution G A downstream_gene_variant UCEC-US 17 1582133 1582133 single base substitution G A exon_variant UCEC-US 17 1582133 1582133 single base substitution G A missense_variant R493W 1477C>T UCEC-US 17 1582133 1582133 single base substitution G A missense_variant R548W 1642C>T UCEC-US 17 1582133 1582133 single base substitution G A upstream_gene_variant UCEC-US 17 1582175 1582175 single base substitution C A downstream_gene_variant UCEC-US 17 1582175 1582175 single base substitution C A splice_region_variant UCEC-US 17 1582175 1582175 single base substitution C A stop_gained E479* 1435G>T UCEC-US 17 1582175 1582175 single base substitution C A stop_gained E534* 1600G>T UCEC-US 17 1582175 1582175 single base substitution C A upstream_gene_variant UCEC-US 17 1582965 1582965 single base substitution C T downstream_gene_variant UCEC-US 17 1582965 1582965 single base substitution C T synonymous_variant R354R 1062G>A UCEC-US 17 1582965 1582965 single base substitution C T synonymous_variant R409R 1227G>A UCEC-US 17 1582965 1582965 single base substitution C T upstream_gene_variant UCEC-US 17 1585166 1585166 single base substitution C T downstream_gene_variant UCEC-US 17 1585166 1585166 single base substitution C T missense_variant A146T 436G>A UCEC-US 17 1585166 1585166 single base substitution C T missense_variant A201T 601G>A UCEC-US 17 1585166 1585166 single base substitution C T upstream_gene_variant UCEC-US 17 1585431 1585431 single base substitution G A downstream_gene_variant UCEC-US 17 1585431 1585431 single base substitution G A intron_variant UCEC-US 17 1585431 1585431 single base substitution G A synonymous_variant S142S 426C>T UCEC-US 17 1585431 1585431 single base substitution G A upstream_gene_variant UCEC-US 17 1585507 1585507 single base substitution G T downstream_gene_variant UCEC-US 17 1585507 1585507 single base substitution G T intron_variant UCEC-US 17 1585507 1585507 single base substitution G T missense_variant P117H 350C>A UCEC-US 17 1585507 1585507 single base substitution G T upstream_gene_variant UCEC-US 17 1586951 1586951 single base substitution G A exon_variant UCEC-US 17 1586951 1586951 single base substitution G A missense_variant R49W 145C>T UCEC-US 17 1586951 1586951 single base substitution G A upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand JJN3 COSM1236120 c.1262C>T p.A421V Substitution - Missense 17:1679636-1679636 - T2944 COSM4718021 c.6660A>G p.P2220P Substitution - coding silent 17:1651301-1651301 - CSCC-27-T COSM4477244 c.2137C>T p.L713F Substitution - Missense 17:1677020-1677020 - sysucc-880T COSM5462598 c.6226A>G p.R2076G Substitution - Missense 17:1653778-1653778 - TCGA-AZ-4315-01 COSM284297 c.5706C>T p.F1902F Substitution - coding silent 17:1656479-1656479 - TCGA-EE-A2A2-06 COSM3514522 c.4834G>A p.E1612K Substitution - Missense 17:1659953-1659953 - TCGA-A2-A0T5-01 COSM3818878 c.3248A>C p.H1083P Substitution - Missense 17:1674493-1674493 - TCGA-FW-A3R5-06 COSM3889347 c.5171C>T p.P1724L Substitution - Missense 17:1658731-1658731 - TCGA-EE-A2A6-06 COSM125614 c.77C>T p.S26L Substitution - Missense 17:1684495-1684495 - YURTHE COSM1709551 c.2173C>A p.P725T Substitution - Missense 17:1676984-1676984 - TCGA-D3-A3C8-06 COSM3514531 c.3069C>T p.N1023N Substitution - coding silent 17:1674672-1674672 - TCGA-CA-6718-01 COSM1381036 c.3075G>A p.T1025T Substitution - coding silent 17:1674666-1674666 - TCGA-FW-A3R5-06 COSM3889346 c.5826C>T p.A1942A Substitution - coding silent 17:1655511-1655511 - PT42 COSM5925948 c.2468C>T p.S823L Substitution - Missense 17:1676291-1676291 - 112229 COSM96157 c.4029C>T p.S1343S Substitution - coding silent 17:1661784-1661784 - TCGA-G2-A3VY-01 COSM3795293 c.4269C>T p.F1423F Substitution - coding silent 17:1661340-1661340 - TCGA-BR-4256-01 COSM4064131 c.1766C>T p.T589M Substitution - Missense 17:1678606-1678606 - TCGA-AA-A010-01 COSM284297 c.5706C>T p.F1902F Substitution - coding silent 17:1656479-1656479 - TCGA-D1-A17Q-01 COSM975791 c.6997C>T p.L2333L Substitution - coding silent 17:1650813-1650813 - T3266 COSM4718025 c.4944delC p.K1649fs*3 Deletion - Frameshift 17:1659843-1659843 - T3262 COSM2738862 c.1410-1G>T p.? Unknown 17:1679207-1679207 - 66 COSM5743804 c.5548C>T p.R1850* Substitution - Nonsense 17:1656719-1656719 - TCGA-G4-6302-01 COSM975835 c.3422G>A p.R1141H Substitution - Missense 17:1673770-1673770 - 234 COSM3731188 c.2630C>T p.A877V Substitution - Missense 17:1675977-1675977 - sysucc-311T COSM5479267 c.1345A>C p.K449Q Substitution - Missense 17:1679355-1679355 - SH-1641 COSM5009690 c.891T>C p.N297N Substitution - coding silent 17:1681030-1681030 - PD7443a COSM3720250 c.5432A>G p.N1811S Substitution - Missense 17:1658326-1658326 - TCGA-AP-A051-01 COSM975832 c.3993C>A p.G1331G Substitution - coding silent 17:1661935-1661935 - SNUH_G26_S1 COSM3680085 c.4785+6C>G p.? Unknown 17:1660426-1660426 - SH-3776 COSM5019798 c.6588T>C p.H2196H Substitution - coding silent 17:1651476-1651476 - SH-5693 COSM5009688 c.2847G>A p.P949P Substitution - coding silent 17:1675645-1675645 - SH-3776 COSM5009690 c.891T>C p.N297N Substitution - coding silent 17:1681030-1681030 - 587338 COSM1222183 c.2374C>T p.H792Y Substitution - Missense 17:1676519-1676519 - TCGA-EI-6917-01 COSM1381036 c.3075G>A p.T1025T Substitution - coding silent 17:1674666-1674666 - HCC141 COSM1609869 c.1340A>G p.Y447C Substitution - Missense 17:1679360-1679360 - BD183T COSM5508173 c.1702A>G p.N568D Substitution - Missense 17:1678779-1678779 - 587256 COSM1222187 c.5191G>A p.A1731T Substitution - Missense 17:1658711-1658711 - 587376 COSM1222185 c.4031A>C p.K1344T Substitution - Missense 17:1661782-1661782 - NCI-H209 COSM41499 c.3205A>G p.N1069D Substitution - Missense 17:1674536-1674536 - STC252 COSM5055235 c.6582C>A p.T2194T Substitution - coding silent 17:1651482-1651482 - HN_00378 COSM125612 c.4774G>A p.D1592N Substitution - Missense 17:1660443-1660443 - S01578 COSM5670355 c.3402G>T p.W1134C Substitution - Missense 17:1673790-1673790 - TCGA-D9-A3Z3-06 COSM3514539 c.1051T>A p.Y351N Substitution - Missense 17:1680773-1680773 - 587338 COSM1163140 c.2602G>A p.E868K Substitution - Missense 17:1676005-1676005 - T155 COSM1176734 c.602C>T p.A201V Substitution - Missense 17:1681871-1681871 - TCGA-AG-A02N-01 COSM265418 c.714_715delCT p.Y239fs*4 Deletion - Frameshift 17:1681629-1681630 - TCGA-24-1469-01 COSM76067 c.2993G>C p.R998P Substitution - Missense 17:1675219-1675219 - HCC122T COSM1609867 c.1985-3C>A p.? Unknown 17:1677175-1677175 - TCGA-HE-7130-01 COSM3988786 c.211C>G p.R71G Substitution - Missense 17:1683591-1683591 - TCGA-EE-A2GI-06 COSM3514515 c.6398C>T p.P2133L Substitution - Missense 17:1651760-1651760 - TCGA-AP-A059-01 COSM975838 c.2903C>T p.T968M Substitution - Missense 17:1675309-1675309 - T2932 COSM4718029 c.3416G>A p.R1139H Substitution - Missense 17:1673776-1673776 - TCGA-AP-A059-01 COSM975800 c.6048C>A p.I2016I Substitution - coding silent 17:1653956-1653956 - T3118 COSM2738786 c.5091G>A p.S1697S Substitution - coding silent 17:1659404-1659404 - TCGA-C8-A1HM-01 COSM436079 c.4183G>C p.E1395Q Substitution - Missense 17:1661630-1661630 - SH-3327 COSM5019358 c.3774+6G>A p.? Unknown 17:1673075-1673075 - TCGA-IR-A3LH-01 COSM4832305 c.6541C>G p.Q2181E Substitution - Missense 17:1651523-1651523 - CRC-06T COSM5456584 c.3325C>T p.L1109L Substitution - coding silent 17:1673867-1673867 - TCGA-BR-6452-01 COSM4064128 c.2558A>G p.K853R Substitution - Missense 17:1676049-1676049 - TCGA-D1-A16J-01 COSM975806 c.5476G>A p.V1826M Substitution - Missense 17:1658282-1658282 - SH-5693 COSM5019798 c.6588T>C p.H2196H Substitution - coding silent 17:1651476-1651476 - 2492726 COSM5725077 c.5379C>A p.T1793T Substitution - coding silent 17:1658379-1658379 - BK0058 COSM4188294 c.4859A>T p.Y1620F Substitution - Missense 17:1659928-1659928 - TCGA-AA-3821-01 COSM294726 c.6052G>A p.A2018T Substitution - Missense 17:1653952-1653952 - 587222 COSM1222182 c.1628C>G p.A543G Substitution - Missense 17:1678853-1678853 - TCGA-66-2785-01 COSM704932 c.6771G>C p.E2257D Substitution - Missense 17:1651190-1651190 - TCGA-GN-A26A-06 COSM2738889 c.292G>A p.A98T Substitution - Missense 17:1682271-1682271 - pfg145T COSM4748526 c.6146A>G p.K2049R Substitution - Missense 17:1653858-1653858 - TCGA-DK-A1A3-01 COSM417184 c.3624C>A p.T1208T Substitution - coding silent 17:1673390-1673390 - TCGA-G9-6338-01 COSM3672356 c.2914G>T p.E972* Substitution - Nonsense 17:1675298-1675298 - P77 COSM5009762 c.5804G>A p.R1935H Substitution - Missense 17:1655533-1655533 - SH-4435 COSM5009689 c.1914C>G p.L638L Substitution - coding silent 17:1677635-1677635 - TCGA-GN-A266-06 COSM3514532 c.2583G>A p.R861R Substitution - coding silent 17:1676024-1676024 - QC2-32-T2 COSM5021156 c.3939G>A p.P1313P Substitution - coding silent 17:1661989-1661989 - YUKAT COSM5385750 c.1843C>T p.R615C Substitution - Missense 17:1678529-1678529 - P100 COSM1381036 c.3075G>A p.T1025T Substitution - coding silent 17:1674666-1674666 - TCGA-AX-A0J1-01 COSM975835 c.3422G>A p.R1141H Substitution - Missense 17:1673770-1673770 - 587232 COSM1222188 c.536C>G p.A179G Substitution - Missense 17:1681937-1681937 - TCGA-BS-A0UA-01 COSM975805 c.5494C>T p.R1832C Substitution - Missense 17:1658264-1658264 - SH-7329 COSM5019573 c.4011A>G p.Q1337Q Substitution - coding silent 17:1661917-1661917 - SC_9008 COSM5572348 c.4105T>A p.Y1369N Substitution - Missense 17:1661708-1661708 - B90-Tumor COSM1749870 c.5623C>G p.H1875D Substitution - Missense 17:1656562-1656562 - TCGA-D1-A16B-01 COSM975792 c.6918C>A p.H2306Q Substitution - Missense 17:1650892-1650892 - SH-9771 COSM5009690 c.891T>C p.N297N Substitution - coding silent 17:1681030-1681030 - HCC113T COSM1609866 c.3926G>T p.S1309I Substitution - Missense 17:1662002-1662002 - 526LT COSM2738768 c.5438G>A p.R1813H Substitution - Missense 17:1658320-1658320 - TCGA-FU-A770-01 COSM4841371 c.5557C>T p.P1853S Substitution - Missense 17:1656710-1656710 - Pat_24_A COSM5851884 c.3280C>T p.R1094C Substitution - Missense 17:1674461-1674461 - TCGA-B5-A11E-01 COSM975807 c.5466C>T p.I1822I Substitution - coding silent 17:1658292-1658292 - T3094 COSM4718035 c.1904G>A p.R635Q Substitution - Missense 17:1677645-1677645 - TCGA-AA-3510-01 COSM1381040 c.1284G>T p.K428N Substitution - Missense 17:1679614-1679614 - SH-3327 COSM5009688 c.2847G>A p.P949P Substitution - coding silent 17:1675645-1675645 - SNU-175 COSM2738889 c.292G>A p.A98T Substitution - Missense 17:1682271-1682271 - TCGA-D1-A15W-01 COSM975804 c.5495G>A p.R1832H Substitution - Missense 17:1658263-1658263 - PDA_059 COSM2738871 c.926G>A p.R309H Substitution - Missense 17:1680995-1680995 - TCGA-HF-7132-01 COSM4064130 c.2260G>A p.A754T Substitution - Missense 17:1676633-1676633 - SH-4435 COSM5009688 c.2847G>A p.P949P Substitution - coding silent 17:1675645-1675645 - SH-3776 COSM5009689 c.1914C>G p.L638L Substitution - coding silent 17:1677635-1677635 - YUZINO COSM1709548 c.6901C>T p.P2301S Substitution - Missense 17:1650909-1650909 - S02299 COSM5690312 c.268G>T p.G90C Substitution - Missense 17:1683534-1683534 - TCGA-E2-A159-01 COSM436073 c.7007G>A p.*2336* Substitution - coding silent 17:1650803-1650803 - SC_9008 COSM5546899 c.517_519delGAG p.E173delE Deletion - In frame 17:1681954-1681956 - LAU165 COSM233189 c.2291G>A p.G764E Substitution - Missense 17:1676602-1676602 - B47 COSM1749867 c.6531G>A p.W2177* Substitution - Nonsense 17:1651533-1651533 - KM12 COSM1679354 c.5137A>G p.S1713G Substitution - Missense 17:1659358-1659358 - TCGA-BR-6563-01 COSM4064119 c.5665C>T p.L1889F Substitution - Missense 17:1656520-1656520 - QC2-32-T2 COSM5009689 c.1914C>G p.L638L Substitution - coding silent 17:1677635-1677635 - TCGA-C8-A132-01 COSM436075 c.6008C>T p.T2003I Substitution - Missense 17:1653996-1653996 - SC_9103 COSM5569617 c.794C>T p.T265M Substitution - Missense 17:1681550-1681550 - TCGA-FV-A3R2-01 COSM4929290 c.2035T>A p.S679T Substitution - Missense 17:1677122-1677122 - 587376 COSM1222186 c.1180T>C p.Y394H Substitution - Missense 17:1679718-1679718 - SH-3133 COSM5009689 c.1914C>G p.L638L Substitution - coding silent 17:1677635-1677635 - 2492720 COSM2738859 c.1615C>T p.R539C Substitution - Missense 17:1678866-1678866 - MDA-MB-435 COSM1679360 c.419A>G p.Y140C Substitution - Missense 17:1682144-1682144 - TCGA-26-5132-01 COSM1381035 c.3206A>G p.N1069S Substitution - Missense 17:1674535-1674535 - TCGA-AB-2904-03 COSM1318536 c.2059G>C p.A687P Substitution - Missense 17:1677098-1677098 - 587220 COSM1222181 c.1226G>A p.R409Q Substitution - Missense 17:1679672-1679672 - PD4137a COSM163765 c.1848C>T p.F616F Substitution - coding silent 17:1678524-1678524 - TCGA-BP-5202-01 COSM472335 c.5789A>G p.Y1930C Substitution - Missense 17:1656396-1656396 - TCGA-B5-A0JY-01 COSM975834 c.3522C>T p.F1174F Substitution - coding silent 17:1673492-1673492 - SH-4435 COSM5019358 c.3774+6G>A p.? Unknown 17:1673075-1673075 - TCGA-DU-7290-01 COSM3969839 c.636G>A p.P212P Substitution - coding silent 17:1681837-1681837 - H650 COSM1194441 c.6173C>A p.T2058N Substitution - Missense 17:1653831-1653831 - TCGA-CS-4938-01 COSM3969837 c.3421C>T p.R1141C Substitution - Missense 17:1673771-1673771 - STC252 COSM5055236 c.6448C>T p.Q2150* Substitution - Nonsense 17:1651710-1651710 - DLBCL-PatientG COSM221374 c.4792G>A p.D1598N Substitution - Missense 17:1659995-1659995 - TCGA-K7-A5RF-01 COSM4909451 c.6572A>G p.Q2191R Substitution - Missense 17:1651492-1651492 - HCC126T COSM3717195 c.2080C>G p.L694V Substitution - Missense 17:1677077-1677077 - TCGA-EB-A5UM-01 COSM3514534 c.2383C>T p.L795L Substitution - coding silent 17:1676510-1676510 - TCGA-61-1728-01 COSM80399 c.4719C>T p.L1573L Substitution - coding silent 17:1660498-1660498 - TCGA-DI-A0WH-01 COSM975795 c.6379T>A p.Y2127N Substitution - Missense 17:1651779-1651779 - TCGA-A8-A0A6-01 COSM3818880 c.2248T>G p.W750G Substitution - Missense 17:1676645-1676645 - TCGA-FV-A23B-01 COSM4913968 c.5279A>T p.E1760V Substitution - Missense 17:1658623-1658623 - TCGA-G2-A3VY-01 COSM3795291 c.4359C>T p.F1453F Substitution - coding silent 17:1661142-1661142 - P100 COSM5009271 c.3876G>T p.E1292D Substitution - Missense 17:1662052-1662052 - TCGA-AP-A0LM-01 COSM975849 c.601G>A p.A201T Substitution - Missense 17:1681872-1681872 - SH-9771 COSM5009689 c.1914C>G p.L638L Substitution - coding silent 17:1677635-1677635 - TCGA-A5-A0GB-01 COSM975846 c.1642C>T p.R548W Substitution - Missense 17:1678839-1678839 - CSCC-40-T COSM4494540 c.4354C>T p.P1452S Substitution - Missense 17:1661147-1661147 - PD22363a COSM5792826 c.4947-8A>G p.? Unknown 17:1659556-1659556 - TARGET-30-PAPZFW COSM1287405 c.6152G>C p.G2051A Substitution - Missense 17:1653852-1653852 - TCGA-A5-A0RA-01 COSM975824 c.4774G>T p.D1592Y Substitution - Missense 17:1660443-1660443 - SH-7166 COSM5020646 c.101-3C>T p.? Unknown 17:1683704-1683704 - PT33 COSM5909616 c.993-8C>T p.? Unknown 17:1680839-1680839 - TCGA-B0-4811-01 COSM472337 c.4628A>T p.N1543I Substitution - Missense 17:1660708-1660708 - S02194 COSM5674816 c.956T>C p.L319S Substitution - Missense 17:1680965-1680965 - TCGA-EE-A181-06 COSM3514540 c.971C>T p.P324L Substitution - Missense 17:1680950-1680950 - BD114T COSM5504240 c.5372A>G p.H1791R Substitution - Missense 17:1658530-1658530 - RK308_C01 COSM3742092 c.4202+6C>T p.? Unknown 17:1661605-1661605 - TCGA-12-0691 COSM2154208 c.6330G>C p.V2110V Substitution - coding silent 17:1653581-1653581 - YUMOOK COSM1709549 c.6821C>T p.P2274L Substitution - Missense 17:1651140-1651140 - PT46 COSM5929762 c.4509-6C>T p.? Unknown 17:1660833-1660833 - SH-3133 COSM5009690 c.891T>C p.N297N Substitution - coding silent 17:1681030-1681030 - LUAD-B00416 COSM330988 c.5135A>G p.H1712R Substitution - Missense 17:1659360-1659360 - T2225 COSM4718034 c.2221C>T p.R741* Substitution - Nonsense 17:1676672-1676672 - MO_1071 COSM5550942 c.4877G>T p.C1626F Substitution - Missense 17:1659910-1659910 - SC_9056 COSM5564185 c.3452G>A p.R1151Q Substitution - Missense 17:1673562-1673562 - SH-1362 COSM5009690 c.891T>C p.N297N Substitution - coding silent 17:1681030-1681030 - AML14 COSM166751 c.5249G>A p.G1750E Substitution - Missense 17:1658653-1658653 - 6115224 COSM5572107 c.5481G>A p.W1827* Substitution - Nonsense 17:1658277-1658277 - SH-1641 COSM5019358 c.3774+6G>A p.? Unknown 17:1673075-1673075 - ME009T COSM223839 c.2932G>A p.E978K Substitution - Missense 17:1675280-1675280 - TCGA-AA-3715-01 COSM269951 c.239A>G p.K80R Substitution - Missense 17:1683563-1683563 - TCGA-BR-A4J4-01 COSM4064136 c.245G>A p.R82H Substitution - Missense 17:1683557-1683557 - ESCC_BICR_032T COSM5431928 c.432G>T p.W144C Substitution - Missense 17:1682131-1682131 - TCGA-EE-A3J5-06 COSM3514541 c.474G>A p.R158R Substitution - coding silent 17:1681999-1681999 - TCGA-DD-A119-01 COSM4919895 c.4351A>G p.N1451D Substitution - Missense 17:1661150-1661150 - HCC141T COSM1609869 c.1340A>G p.Y447C Substitution - Missense 17:1679360-1679360 - TCGA-DG-A2KK-01 COSM4828566 c.5938G>A p.E1980K Substitution - Missense 17:1655399-1655399 - TTC466 COSM4579464 c.183G>C p.M61I Substitution - Missense 17:1683619-1683619 - MBRep_T2 COSM215669 c.2995C>T p.L999F Substitution - Missense 17:1675217-1675217 - SH-3133 COSM5019798 c.6588T>C p.H2196H Substitution - coding silent 17:1651476-1651476 - HCT15 COSM1679358 c.2779T>C p.W927R Substitution - Missense 17:1675713-1675713 - TCGA-B8-4153-01 COSM472336 c.5517G>T p.W1839C Substitution - Missense 17:1656750-1656750 - MDA-N COSM1679360 c.419A>G p.Y140C Substitution - Missense 17:1682144-1682144 - SH-3776 COSM5019358 c.3774+6G>A p.? Unknown 17:1673075-1673075 - TCGA-22-5477-01 COSM704920 c.1375C>G p.L459V Substitution - Missense 17:1679325-1679325 - TCGA-C5-A2LX-01 COSM4827512 c.5248G>C p.G1750R Substitution - Missense 17:1658654-1658654 - YUMOOK COSM1709550 c.4270C>T p.Q1424* Substitution - Nonsense 17:1661339-1661339 - HOP-62 COSM1679357 c.3642G>A p.W1214* Substitution - Nonsense 17:1673372-1673372 - B89-4-Tumor COSM1749868 c.5928G>T p.W1976C Substitution - Missense 17:1655409-1655409 - TCGA-B0-5098-01 COSM1493765 c.5999C>T p.A2000V Substitution - Missense 17:1654005-1654005 - TCGA-AP-A0LM-01 COSM975845 c.1778G>A p.R593Q Substitution - Missense 17:1678594-1678594 - CSCC-11-T COSM4468085 c.1525C>T p.H509Y Substitution - Missense 17:1679091-1679091 - SH-5693 COSM5009690 c.891T>C p.N297N Substitution - coding silent 17:1681030-1681030 - D21 COSM5007782 c.2564G>A p.R855Q Substitution - Missense 17:1676043-1676043 - ICGC_MB63 COSM3764585 c.5001C>T p.R1667R Substitution - coding silent 17:1659494-1659494 - TCGA-D1-A17Q-01 COSM975839 c.2798G>A p.R933H Substitution - Missense 17:1675694-1675694 - YUKAT COSM5385744 c.4938T>C p.A1646A Substitution - coding silent 17:1659849-1659849 - Case_11 COSM1724987 c.3921G>A p.M1307I Substitution - Missense 17:1662007-1662007 - TCGA-BH-A0GZ-01 COSM436078 c.4463C>T p.T1488I Substitution - Missense 17:1661038-1661038 - HCC122T COSM1609868 c.1985-9T>C p.? Unknown 17:1677181-1677181 - S00932 COSM314484 c.5376+3G>T p.? Unknown 17:1658523-1658523 - B89-4 COSM1749869 c.5927G>T p.W1976L Substitution - Missense 17:1655410-1655410 - SNUH_G37_S1 COSM3680087 c.4757A>C p.H1586P Substitution - Missense 17:1660460-1660460 - P12 COSM5009691 c.637T>C p.L213L Substitution - coding silent 17:1681836-1681836 - DN1401C COSM5960779 c.3196C>T p.Q1066* Substitution - Nonsense 17:1674545-1674545 - TCGA-A6-6781-01 COSM1381034 c.3582C>T p.C1194C Substitution - coding silent 17:1673432-1673432 - TCGA-D7-5577-01 COSM4064126 c.3082T>A p.Y1028N Substitution - Missense 17:1674659-1674659 - SH-1679 COSM5009690 c.891T>C p.N297N Substitution - coding silent 17:1681030-1681030 - TCGA-B5-A11E-01 COSM975850 c.426C>T p.S142S Substitution - coding silent 17:1682137-1682137 - D5 COSM3361993 c.5612C>T p.P1871L Substitution - Missense 17:1656655-1656655 - sysucc-880T COSM5462599 c.2388+6G>A p.? Unknown 17:1676499-1676499 - TCGA-B5-A0JY-01 COSM975794 c.6534C>A p.I2178I Substitution - coding silent 17:1651530-1651530 - TCGA-B5-A11E-01 COSM975843 c.2342G>A p.R781Q Substitution - Missense 17:1676551-1676551 - CSCC-27-T COSM4500688 c.5715C>T p.L1905L Substitution - coding silent 17:1656470-1656470 - CSCC-49-T COSM4491916 c.3886C>T p.Q1296* Substitution - Nonsense 17:1662042-1662042 - 2492700 COSM5600291 c.5291C>T p.S1764F Substitution - Missense 17:1658611-1658611 - TCGA-EJ-7321-01 COSM3783023 c.4689C>T p.H1563H Substitution - coding silent 17:1660528-1660528 - SC_9012 COSM5558897 c.6117G>C p.L2039L Substitution - coding silent 17:1653887-1653887 - ICGC_PA46 COSM3670206 c.2025G>A p.Q675Q Substitution - coding silent 17:1677132-1677132 - TCGA-D1-A176-01 COSM975825 c.4567C>T p.R1523* Substitution - Nonsense 17:1660769-1660769 - 587342 COSM1222184 c.6854-2A>C p.? Unknown 17:1650958-1650958 - TCGA-AP-A0LM-01 COSM975798 c.6154G>A p.D2052N Substitution - Missense 17:1653850-1653850 - TCGA-FD-A3B3-01 COSM1302423 c.5157C>T p.F1719F Substitution - coding silent 17:1658745-1658745 - BD57T COSM5509620 c.4240C>T p.R1414C Substitution - Missense 17:1661369-1661369 - TCGA-FW-A3TU-06 COSM3514538 c.1424C>T p.S475F Substitution - Missense 17:1679192-1679192 - P100 COSM5009273 c.2904G>A p.T968T Substitution - coding silent 17:1675308-1675308 - ccRCC-14 COSM975802 c.5624A>G p.H1875R Substitution - Missense 17:1656561-1656561 - 2492723 COSM2738859 c.1615C>T p.R539C Substitution - Missense 17:1678866-1678866 - TCGA-AK-3445-01 COSM3361993 c.5612C>T p.P1871L Substitution - Missense 17:1656655-1656655 - CSCC-56-T COSM4496311 c.4722C>T p.I1574I Substitution - coding silent 17:1660495-1660495 - TCGA-HU-A4GQ-01 COSM2738848 c.2056C>T p.R686W Substitution - Missense 17:1677101-1677101 - TCGA-A5-A0GV-01 COSM975805 c.5494C>T p.R1832C Substitution - Missense 17:1658264-1658264 - TCGA-BH-A18G-01 COSM3818879 c.2287C>T p.R763* Substitution - Nonsense 17:1676606-1676606 - 254891 COSM3724809 c.4039G>A p.D1347N Substitution - Missense 17:1661774-1661774 - TCGA-EK-A2R8-01 COSM4822707 c.6315C>T p.I2105I Substitution - coding silent 17:1653596-1653596 - T191 COSM4718026 c.4781G>T p.C1594F Substitution - Missense 17:1660436-1660436 - 2492725 COSM5725077 c.5379C>A p.T1793T Substitution - coding silent 17:1658379-1658379 - TCGA-GN-A26C-01 COSM3514542 c.397C>T p.P133S Substitution - Missense 17:1682166-1682166 - TCGA-85-6561-01 COSM704919 c.1290G>C p.W430C Substitution - Missense 17:1679410-1679410 - CSCC-18-T COSM4496348 c.4731C>T p.F1577F Substitution - coding silent 17:1660486-1660486 - 2334194 COSM41499 c.3205A>G p.N1069D Substitution - Missense 17:1674536-1674536 - Gp2D COSM4627495 c.6468C>T p.T2156T Substitution - coding silent 17:1651690-1651690 - PA285 COSM1163140 c.2602G>A p.E868K Substitution - Missense 17:1676005-1676005 - TCGA-AX-A0J1-01 COSM975848 c.1227G>A p.R409R Substitution - coding silent 17:1679671-1679671 - C91 COSM4444570 c.3001G>A p.V1001M Substitution - Missense 17:1675211-1675211 - NCI-H835 COSM2738728 c.5876C>T p.T1959I Substitution - Missense 17:1655461-1655461 - SH-5693 COSM5019358 c.3774+6G>A p.? Unknown 17:1673075-1673075 - T3225 COSM4718030 c.3381C>T p.G1127G Substitution - coding silent 17:1673811-1673811 - SH-9161 COSM5020646 c.101-3C>T p.? Unknown 17:1683704-1683704 - SH-1641 COSM5009688 c.2847G>A p.P949P Substitution - coding silent 17:1675645-1675645 - SH-1439 COSM5009690 c.891T>C p.N297N Substitution - coding silent 17:1681030-1681030 - CSCC-29-T COSM4563348 c.96G>A p.E32E Substitution - coding silent 17:1684476-1684476 - TCGA-AA-3680-01 COSM268012 c.384delC p.F128fs*23 Deletion - Frameshift 17:1682179-1682179 - TCGA-CF-A1HR-01 COSM417182 c.1539C>T p.L513L Substitution - coding silent 17:1679077-1679077 - TCGA-A8-A095-01 COSM436081 c.1877G>T p.G626V Substitution - Missense 17:1677672-1677672 - UM-SCC-11B COSM4598054 c.3716G>A p.R1239H Substitution - Missense 17:1673139-1673139 - 403 COSM4429904 c.2062G>T p.A688S Substitution - Missense 17:1677095-1677095 - I2L-P7-Tumor-Organoid COSM5364468 c.806T>G p.L269R Substitution - Missense 17:1681538-1681538 - TCGA-D8-A1J8-01 COSM3818871 c.6517G>A p.E2173K Substitution - Missense 17:1651547-1651547 - TCGA-HU-A4G8-01 COSM4064118 c.5763C>T p.D1921D Substitution - coding silent 17:1656422-1656422 - TCGA-D7-6526-01 COSM4064122 c.4959C>T p.D1653D Substitution - coding silent 17:1659536-1659536 - TCGA-BR-6452-01 COSM4064124 c.3711G>A p.M1237I Substitution - Missense 17:1673144-1673144 - SH-3327 COSM5009690 c.891T>C p.N297N Substitution - coding silent 17:1681030-1681030 - CSCC-29-T COSM4505339 c.6902C>T p.P2301L Substitution - Missense 17:1650908-1650908 - PCSI_0345_Pa_P_526 COSM4809266 c.5901C>T p.I1967I Substitution - coding silent 17:1655436-1655436 - HCC103T COSM5818410 c.5589C>T p.V1863V Substitution - coding silent 17:1656678-1656678 - TCGA-CM-4743-01 COSM1381023 c.6179G>C p.S2060T Substitution - Missense 17:1653825-1653825 - TCGA-BF-A3DM-01 COSM3889348 c.4620G>T p.P1540P Substitution - coding silent 17:1660716-1660716 - SH-1679 COSM5019573 c.4011A>G p.Q1337Q Substitution - coding silent 17:1661917-1661917 - Patient_2 COSM5346886 c.5453T>G p.F1818C Substitution - Missense 17:1658305-1658305 - T3658 COSM2738768 c.5438G>A p.R1813H Substitution - Missense 17:1658320-1658320 - TCGA-BR-6566-01 COSM4064125 c.3576C>T p.F1192F Substitution - coding silent 17:1673438-1673438 - PGBM07PT COSM1579876 c.4833G>T p.K1611N Substitution - Missense 17:1659954-1659954 - TCGA-CH-5750-01 COSM1128822 c.5615T>G p.L1872R Substitution - Missense 17:1656652-1656652 - TCGA-EE-A29A-06 COSM3514528 c.4183G>A p.E1395K Substitution - Missense 17:1661630-1661630 - SH-3133 COSM5009688 c.2847G>A p.P949P Substitution - coding silent 17:1675645-1675645 - HN_00378 COSM125613 c.4772T>G p.M1591R Substitution - Missense 17:1660445-1660445 - SH-1679 COSM5019358 c.3774+6G>A p.? Unknown 17:1673075-1673075 - P129 COSM5010217 c.5061C>T p.Y1687Y Substitution - coding silent 17:1659434-1659434 - T3446 COSM1381024 c.5008delG p.D1670fs*23 Deletion - Frameshift 17:1659487-1659487 - TCGA-G4-6628-01 COSM1381038 c.2716G>A p.V906I Substitution - Missense 17:1675776-1675776 - TCGA-EM-A3FN-01 COSM3370623 c.2437A>G p.T813A Substitution - Missense 17:1676322-1676322 - T3535 COSM4718036 c.1795A>G p.M599V Substitution - Missense 17:1678577-1678577 - 86785 COSM95092 c.2458C>T p.R820C Substitution - Missense 17:1676301-1676301 - TCGA-A2-A25B-01 COSM1479261 c.1638G>A p.L546L Substitution - coding silent 17:1678843-1678843 - 2492703 COSM5600291 c.5291C>T p.S1764F Substitution - Missense 17:1658611-1658611 - SH-1679 COSM5009688 c.2847G>A p.P949P Substitution - coding silent 17:1675645-1675645 - QC2-32-T2 COSM5009690 c.891T>C p.N297N Substitution - coding silent 17:1681030-1681030 - MOLT-4 COSM1679356 c.3907C>G p.L1303V Substitution - Missense 17:1662021-1662021 - TCGA-34-5927-01 COSM704917 c.587A>T p.D196V Substitution - Missense 17:1681886-1681886 - TCGA-B0-5119-01 COSM472339 c.1373C>T p.A458V Substitution - Missense 17:1679327-1679327 - TCGA-IR-A3LH-01 COSM4833531 c.6507C>G p.L2169L Substitution - coding silent 17:1651651-1651651 - TCGA-FS-A1ZZ-06 COSM3514543 c.244C>A p.R82S Substitution - Missense 17:1683558-1683558 - 2492722 COSM2738859 c.1615C>T p.R539C Substitution - Missense 17:1678866-1678866 - TCGA-A5-A0VP-01 COSM178201 c.5539G>A p.A1847T Substitution - Missense 17:1656728-1656728 - CHC2213T COSM4801168 c.2493C>G p.S831S Substitution - coding silent 17:1676266-1676266 - T3262 COSM4718022 c.6570C>A p.P2190P Substitution - coding silent 17:1651494-1651494 - T144 COSM307669 c.3593C>T p.P1198L Substitution - Missense 17:1673421-1673421 - C135 COSM2738768 c.5438G>A p.R1813H Substitution - Missense 17:1658320-1658320 - TCGA-BF-A1Q0-01 COSM3514533 c.2512T>C p.L838L Substitution - coding silent 17:1676247-1676247 - TCGA-BC-A69H-01 COSM4918983 c.3670C>T p.R1224C Substitution - Missense 17:1673185-1673185 - P12 COSM5009688 c.2847G>A p.P949P Substitution - coding silent 17:1675645-1675645 - SH-1439 COSM5009689 c.1914C>G p.L638L Substitution - coding silent 17:1677635-1677635 - TCGA-BR-8368-01 COSM4064137 c.1A>G p.M1V Substitution - Missense 17:1684571-1684571 - BK0019 COSM4186167 c.1237C>A p.L413I Substitution - Missense 17:1679661-1679661 - BD72T COSM5513236 c.4150C>T p.R1384W Substitution - Missense 17:1661663-1661663 - SH-1439 COSM5019358 c.3774+6G>A p.? Unknown 17:1673075-1673075 - CHC2213T COSM4801168 c.2493C>G p.S831S Substitution - coding silent 17:1676266-1676266 - TCGA-AA-3680-01 COSM268011 c.4241G>A p.R1414H Substitution - Missense 17:1661368-1661368 - RK223_C01 COSM4779146 c.1660A>G p.T554A Substitution - Missense 17:1678821-1678821 - T3724 COSM4718024 c.4965C>A p.T1655T Substitution - coding silent 17:1659530-1659530 - TCGA-D1-A17U-01 COSM975819 c.5165G>A p.S1722N Substitution - Missense 17:1658737-1658737 - STC246 COSM5055237 c.5376G>A p.K1792K Substitution - coding silent 17:1658526-1658526 - P12 COSM5009689 c.1914C>G p.L638L Substitution - coding silent 17:1677635-1677635 - 112190 COSM96156 c.6657G>T p.T2219T Substitution - coding silent 17:1651304-1651304 - TCGA-EE-A2GU-06 COSM3514516 c.5845C>T p.R1949W Substitution - Missense 17:1655492-1655492 - TCGA-DD-A1E9-01 COSM4912384 c.4568G>T p.R1523L Substitution - Missense 17:1660768-1660768 - C467 COSM4442022 c.1309G>T p.A437S Substitution - Missense 17:1679391-1679391 - TCGA-EE-A3JD-06 COSM284297 c.5706C>T p.F1902F Substitution - coding silent 17:1656479-1656479 - SH-1641 COSM5009689 c.1914C>G p.L638L Substitution - coding silent 17:1677635-1677635 - SH-3327 COSM5009689 c.1914C>G p.L638L Substitution - coding silent 17:1677635-1677635 - TCGA-D1-A161-01 COSM975805 c.5494C>T p.R1832C Substitution - Missense 17:1658264-1658264 - TCGA-A3-3324-01 COSM1135881 c.5624A>C p.H1875P Substitution - Missense 17:1656561-1656561 - B89-4-Tumor COSM1749869 c.5927G>T p.W1976L Substitution - Missense 17:1655410-1655410 - TCGA-26-5132 COSM1381035 c.3206A>G p.N1069S Substitution - Missense 17:1674535-1674535 - BD57T COSM5510862 c.73_74insT p.M25fs*60 Insertion - Frameshift 17:1684498-1684499 - MOLT-4 COSM1679355 c.3955C>T p.P1319S Substitution - Missense 17:1661973-1661973 - QC2-25-T2 COSM5653361 c.2000G>T p.G667V Substitution - Missense 17:1677157-1677157 - TCGA-D1-A0ZQ-01 COSM975801 c.5625_5627delCTT p.H1875_L1876>Q Complex - deletion inframe 17:1656558-1656560 - TCGA-D1-A16X-01 COSM975841 c.2476C>A p.P826T Substitution - Missense 17:1676283-1676283 - SC_9032 COSM5558733 c.5119C>T p.L1707L Substitution - coding silent 17:1659376-1659376 - TCGA-G2-A3VY-01 COSM3795292 c.4348C>G p.Q1450E Substitution - Missense 17:1661153-1661153 - STC291 COSM5055238 c.2797C>T p.R933C Substitution - Missense 17:1675695-1675695 - 2492702 COSM5600291 c.5291C>T p.S1764F Substitution - Missense 17:1658611-1658611 - SH-1362 COSM5009688 c.2847G>A p.P949P Substitution - coding silent 17:1675645-1675645 - TCGA-FS-A1Z7-06 COSM3514523 c.4756C>T p.H1586Y Substitution - Missense 17:1660461-1660461 - TCGA-AG-3594-01 COSM287990 c.2646G>A p.K882K Substitution - coding silent 17:1675961-1675961 - 159 COSM1381038 c.2716G>A p.V906I Substitution - Missense 17:1675776-1675776 - TCGA-FP-8631-01 COSM4064127 c.2572C>T p.Q858* Substitution - Nonsense 17:1676035-1676035 - 2290930 COSM4440487 c.3938delC p.P1313fs*36 Deletion - Frameshift 17:1661990-1661990 - SH-7032 COSM5019573 c.4011A>G p.Q1337Q Substitution - coding silent 17:1661917-1661917 - 116 COSM5013061 c.1772T>C p.M591T Substitution - Missense 17:1678600-1678600 - Pat_24_B COSM5851883 c.4117C>T p.Q1373* Substitution - Nonsense 17:1661696-1661696 - T276 COSM4718031 c.3335G>A p.R1112H Substitution - Missense 17:1673857-1673857 - TCGA-D1-A174-01 COSM975844 c.2227G>A p.V743M Substitution - Missense 17:1676666-1676666 - TCGA-14-0790-01 COSM3402622 c.3440T>C p.V1147A Substitution - Missense 17:1673752-1673752 - TCGA-CJ-4923-01 COSM472338 c.2653C>T p.L885F Substitution - Missense 17:1675954-1675954 - HT115 COSM2738852 c.1807C>T p.R603C Substitution - Missense 17:1678565-1678565 - S00932 COSM314484 c.5376+3G>T p.? Unknown 17:1658523-1658523 - TCGA-BS-A0UJ-01 COSM975793 c.6753C>T p.Y2251Y Substitution - coding silent 17:1651208-1651208 - TCGA-CG-4437-01 COSM4064123 c.4019T>G p.L1340R Substitution - Missense 17:1661909-1661909 - 169 COSM3729665 c.4295A>G p.Y1432C Substitution - Missense 17:1661314-1661314 - TCGA-AP-A051-01 COSM975833 c.3849G>A p.E1283E Substitution - coding silent 17:1662079-1662079 - Pat_24_B COSM1381024 c.5008delG p.D1670fs*23 Deletion - Frameshift 17:1659487-1659487 - HCC126 COSM3717195 c.2080C>G p.L694V Substitution - Missense 17:1677077-1677077 - sysucc-880T COSM4186167 c.1237C>A p.L413I Substitution - Missense 17:1679661-1679661 - LUAD-RT-S01477 COSM377500 c.4947G>T p.K1649N Substitution - Missense 17:1659548-1659548 - 03-P1004 COSM4579462 c.1083T>C p.H361H Substitution - coding silent 17:1680741-1680741 - TCGA-B4-5836-01 COSM1493763 c.3385A>T p.N1129Y Substitution - Missense 17:1673807-1673807 - TCGA-DJ-A1QE-01 COSM3370622 c.4333T>G p.Y1445D Substitution - Missense 17:1661276-1661276 - HCT15 COSM2738830 c.4131C>T p.S1377S Substitution - coding silent 17:1661682-1661682 - T2940 COSM4718032 c.3167A>G p.H1056R Substitution - Missense 17:1674574-1674574 - SH-5693 COSM5009689 c.1914C>G p.L638L Substitution - coding silent 17:1677635-1677635 - TCGA-HU-A4GN-01 COSM4064129 c.2533C>T p.R845W Substitution - Missense 17:1676226-1676226 - TCGA-AX-A0J0-01 COSM975847 c.1600G>T p.E534* Substitution - Nonsense 17:1678881-1678881 - TCGA-AX-A0J0-01 COSM975836 c.3148T>C p.L1050L Substitution - coding silent 17:1674593-1674593 - BD124T COSM5493500 c.810T>C p.N270N Substitution - coding silent 17:1681534-1681534 - P12 COSM5009690 c.891T>C p.N297N Substitution - coding silent 17:1681030-1681030 - sysucc-783T COSM5484073 c.6715C>T p.R2239C Substitution - Missense 17:1651246-1651246 - B47-Tumor COSM1749867 c.6531G>A p.W2177* Substitution - Nonsense 17:1651533-1651533 - HN_62493 COSM125614 c.77C>T p.S26L Substitution - Missense 17:1684495-1684495 - T1743 COSM4718023 c.5471C>T p.T1824M Substitution - Missense 17:1658287-1658287 - NYU274 COSM4770982 c.3059A>T p.K1020M Substitution - Missense 17:1675153-1675153 - TCGA-B5-A11J-01 COSM975842 c.2459G>A p.R820H Substitution - Missense 17:1676300-1676300 - T3503 COSM4444570 c.3001G>A p.V1001M Substitution - Missense 17:1675211-1675211 - CSCC-35-T COSM4507013 c.735C>T p.L245L Substitution - coding silent 17:1681609-1681609 - TCGA-BR-8360-01 COSM4064135 c.522G>A p.P174P Substitution - coding silent 17:1681951-1681951 - TCGA-AB-3001-03 COSM166751 c.5249G>A p.G1750E Substitution - Missense 17:1658653-1658653 - TCGA-EJ-A65D-01 COSM4392679 c.5512A>G p.K1838E Substitution - Missense 17:1656755-1656755 - KM12 COSM1679354 c.5137A>G p.S1713G Substitution - Missense 17:1659358-1659358 - MOLT-4 COSM1679359 c.988A>G p.T330A Substitution - Missense 17:1680933-1680933 - B22-Tumor COSM1749873 c.1914C>T p.L638L Substitution - coding silent 17:1677635-1677635 - SH-1679 COSM5009689 c.1914C>G p.L638L Substitution - coding silent 17:1677635-1677635 - YUJUBE COSM5385749 c.4355C>T p.P1452L Substitution - Missense 17:1661146-1661146 - T94 COSM238025 c.3456G>A p.A1152A Substitution - coding silent 17:1673558-1673558 - ICGC_MB63 COSM3764585 c.5001C>T p.R1667R Substitution - coding silent 17:1659494-1659494 - B90 COSM1749870 c.5623C>G p.H1875D Substitution - Missense 17:1656562-1656562 - TCGA-FS-A1Z3-06 COSM3514529 c.3375C>T p.I1125I Substitution - coding silent 17:1673817-1673817 - 66 COSM5743805 c.3671G>A p.R1224H Substitution - Missense 17:1673184-1673184 - DN14065 COSM5962794 c.3414C>T p.A1138A Substitution - coding silent 17:1673778-1673778 - CMLPh-001 COSM4424128 c.4720A>C p.I1574L Substitution - Missense 17:1660497-1660497 - PD4847a COSM5778142 c.4473G>A p.K1491K Substitution - coding silent 17:1661028-1661028 - OSCC-GB_00910111 COSM4888133 c.3120C>A p.I1040I Substitution - coding silent 17:1674621-1674621 - TCGA-AX-A0J1-01 COSM975831 c.4168G>A p.A1390T Substitution - Missense 17:1661645-1661645 - Pat_59_A COSM2738704 c.6796C>T p.R2266C Substitution - Missense 17:1651165-1651165 - TCGA-D9-A6EC-06 COSM4404101 c.1805T>G p.I602S Substitution - Missense 17:1678567-1678567 - T613 COSM2738848 c.2056C>T p.R686W Substitution - Missense 17:1677101-1677101 - ICGC_PA46 COSM3670206 c.2025G>A p.Q675Q Substitution - coding silent 17:1677132-1677132 - SH-3133 COSM5019358 c.3774+6G>A p.? Unknown 17:1673075-1673075 - 19 COSM5747782 c.1100G>A p.S367N Substitution - Missense 17:1679798-1679798 - TCGA-D1-A17Q-01 COSM975845 c.1778G>A p.R593Q Substitution - Missense 17:1678594-1678594 - TCGA-FN-7833-01 COSM3969836 c.5991G>A p.V1997V Substitution - coding silent 17:1654013-1654013 - HCC122 COSM1609868 c.1985-9T>C p.? Unknown 17:1677181-1677181 - TCGA-D1-A103-01 COSM975840 c.2752A>T p.T918S Substitution - Missense 17:1675740-1675740 - SH-1439 COSM5021156 c.3939G>A p.P1313P Substitution - coding silent 17:1661989-1661989 - C135 COSM4617723 c.3483G>A p.L1161L Substitution - coding silent 17:1673531-1673531 - TCGA-EE-A3JD-06 COSM4396970 c.5052C>T p.F1684F Substitution - coding silent 17:1659443-1659443 - LUAD_E00522 COSM352635 c.1174C>T p.P392S Substitution - Missense 17:1679724-1679724 - LIM2551 COSM4644034 c.5475C>T p.S1825S Substitution - coding silent 17:1658283-1658283 - TCGA-BR-4368-01 COSM4064134 c.719G>A p.R240H Substitution - Missense 17:1681625-1681625 - HCC062T COSM5820848 c.6241G>T p.A2081S Substitution - Missense 17:1653670-1653670 - LUAD-F00134 COSM339954 c.3471C>T p.I1157I Substitution - coding silent 17:1673543-1673543 - TCGA-EE-A2MR-06 COSM3514530 c.3297C>T p.F1099F Substitution - coding silent 17:1674444-1674444 - 1604875 COSM141481 c.595G>A p.E199K Substitution - Missense 17:1681878-1681878 - TCGA-AA-A010-01 COSM284298 c.707C>T p.S236L Substitution - Missense 17:1681637-1681637 - RK180_C02 COSM1630063 c.2983A>T p.R995W Substitution - Missense 17:1675229-1675229 - T55 COSM4718028 c.3417C>T p.R1139R Substitution - coding silent 17:1673775-1673775 - SH-1439 COSM5021174 c.993-7A>G p.? Unknown 17:1680838-1680838 - SH-1439 COSM5021164 c.6294G>A p.K2098K Substitution - coding silent 17:1653617-1653617 - ESCC_128 COSM5641635 c.3478C>T p.R1160C Substitution - Missense 17:1673536-1673536 - OSCC-GB_00830111 COSM4889145 c.6891G>T p.Q2297H Substitution - Missense 17:1650919-1650919 - TCGA-BS-A0UV-01 COSM975830 c.4253G>A p.R1418Q Substitution - Missense 17:1661356-1661356 - LUAD-NYU1219 COSM369928 c.3310G>T p.D1104Y Substitution - Missense 17:1673882-1673882 - U2940 COSM5621609 c.4936G>A p.A1646T Substitution - Missense 17:1659851-1659851 - TCGA-EE-A2GC-06 COSM3514537 c.1683C>T p.H561H Substitution - coding silent 17:1678798-1678798 - SH-3776 COSM5009688 c.2847G>A p.P949P Substitution - coding silent 17:1675645-1675645 - PTC-7C COSM4129607 c.3536G>T p.S1179I Substitution - Missense 17:1673478-1673478 - TCGA-BP-5004-01 COSM472341 c.208A>C p.I70L Substitution - Missense 17:1683594-1683594 - TCGA-22-5472-01 COSM704924 c.3416G>T p.R1139L Substitution - Missense 17:1673776-1673776 - TCGA-GM-A2DO-01 COSM3818872 c.5360G>C p.R1787T Substitution - Missense 17:1658542-1658542 - TCGA-C8-A12T-01 COSM436080 c.3017C>T p.A1006V Substitution - Missense 17:1675195-1675195 - CSCC-44-T COSM4492197 c.3933C>T p.F1311F Substitution - coding silent 17:1661995-1661995 - PARGHW COSM5005630 c.3898A>G p.K1300E Substitution - Missense 17:1662030-1662030 - CSCC-31-T COSM4488950 c.3404C>T p.P1135L Substitution - Missense 17:1673788-1673788 - HCC113 COSM1609866 c.3926G>T p.S1309I Substitution - Missense 17:1662002-1662002 - TCGA-DB-A64L-01 COSM3969838 c.3041A>G p.N1014S Substitution - Missense 17:1675171-1675171 - SNUH_G26_S1 COSM3680086 c.4784A>G p.Q1595R Substitution - Missense 17:1660433-1660433 - T3174 COSM4718033 c.2532G>T p.E844D Substitution - Missense 17:1676227-1676227 - TCGA-AP-A0LM-01 COSM975851 c.350C>A p.P117H Substitution - Missense 17:1682213-1682213 - TCGA-EW-A1P6-01 COSM1479260 c.3584G>A p.R1195H Substitution - Missense 17:1673430-1673430 - TCGA-BG-A0MO-01 COSM975802 c.5624A>G p.H1875R Substitution - Missense 17:1656561-1656561 - N744T COSM236549 c.4752G>T p.K1584N Substitution - Missense 17:1660465-1660465 - TCGA-B0-4837-01 COSM3361995 c.862C>G p.L288V Substitution - Missense 17:1681482-1681482 - TCGA-G2-A3VY-01 COSM3795294 c.4145C>G p.S1382C Substitution - Missense 17:1661668-1661668 - ESCC_68 COSM5633875 c.1447C>G p.Q483E Substitution - Missense 17:1679169-1679169 - HCT-15 COSM1679358 c.2779T>C p.W927R Substitution - Missense 17:1675713-1675713 - TCGA-AO-A128-01 COSM3818881 c.1971C>A p.A657A Substitution - coding silent 17:1677578-1677578 - CSCC-29-T COSM4501129 c.5812C>T p.L1938L Substitution - coding silent 17:1655525-1655525 - SH-1439 COSM5019798 c.6588T>C p.H2196H Substitution - coding silent 17:1651476-1651476 - TCGA-22-1012-01 COSM704916 c.511G>T p.D171Y Substitution - Missense 17:1681962-1681962 - SH-9771 COSM5009688 c.2847G>A p.P949P Substitution - coding silent 17:1675645-1675645 - TCGA-C8-A1HF-01 COSM436077 c.5425A>G p.I1809V Substitution - Missense 17:1658333-1658333 - TCGA-D1-A167-01 COSM975852 c.145C>T p.R49W Substitution - Missense 17:1683657-1683657 - TCGA-EE-A3AB-06 COSM3514536 c.1774T>C p.Y592H Substitution - Missense 17:1678598-1678598 - PTC_285 COSM5958775 c.3663delT p.K1222fs*39 Deletion - Frameshift 17:1673192-1673192 - T2578 COSM4718027 c.3602G>A p.R1201H Substitution - Missense 17:1673412-1673412 - T2957 COSM4718037 c.457C>T p.R153* Substitution - Nonsense 17:1682016-1682016 - TCGA-ER-A19F-06 COSM3514535 c.2186C>T p.P729L Substitution - Missense 17:1676707-1676707 - TCGA-85-6561-01 COSM704918 c.878G>T p.W293L Substitution - Missense 17:1681043-1681043 - TCGA-18-3409-01 COSM704921 c.1593C>T p.T531T Substitution - coding silent 17:1679023-1679023 - SH-9771 COSM5019358 c.3774+6G>A p.? Unknown 17:1673075-1673075 - LP6007504-DNA_A01 COSM4408805 c.3802A>C p.I1268L Substitution - Missense 17:1662126-1662126 - TCGA-EB-A3Y7-01 COSM3514517 c.5603T>G p.M1868R Substitution - Missense 17:1656664-1656664 - CSCC-18-T COSM4452453 c.1868A>T p.K623M Substitution - Missense 17:1677681-1677681 - TCGA-BQ-5889-01 COSM3988785 c.4340T>A p.V1447D Substitution - Missense 17:1661161-1661161 - TCGA-D5-6930-01 COSM1381024 c.5008delG p.D1670fs*23 Deletion - Frameshift 17:1659487-1659487 - pfg016T COSM1640597 c.2564G>T p.R855L Substitution - Missense 17:1676043-1676043 - SH-1362 COSM5019358 c.3774+6G>A p.? Unknown 17:1673075-1673075 - P9 COSM5009856 c.5412C>T p.N1804N Substitution - coding silent 17:1658346-1658346 - Pat_41_B COSM5851879 c.6151G>A p.G2051S Substitution - Missense 17:1653853-1653853 - SH-1362 COSM5009689 c.1914C>G p.L638L Substitution - coding silent 17:1677635-1677635 - TCGA-EK-A2R8-01 COSM4822733 c.6030C>T p.I2010I Substitution - coding silent 17:1653974-1653974 - 2492701 COSM5600291 c.5291C>T p.S1764F Substitution - Missense 17:1658611-1658611 - 6115224 COSM5572106 c.5480G>A p.W1827* Substitution - Nonsense 17:1658278-1658278 - DLBCL-PatientG COSM221354 c.1291T>G p.Y431D Substitution - Missense 17:1679409-1679409 - 403 COSM4429903 c.2063C>T p.A688V Substitution - Missense 17:1677094-1677094 - ESCC-184T COSM3937261 c.5427C>T p.I1809I Substitution - coding silent 17:1658331-1658331 - 2492706 COSM5716791 c.1024A>G p.T342A Substitution - Missense 17:1680800-1680800 - 2492724 COSM5725077 c.5379C>A p.T1793T Substitution - coding silent 17:1658379-1658379 - SH-1439 COSM5009688 c.2847G>A p.P949P Substitution - coding silent 17:1675645-1675645 - LUAD-RT-S01818 COSM383889 c.5042G>T p.R1681L Substitution - Missense 17:1659453-1659453 - HN_62832 COSM121654 c.6270C>T p.I2090I Substitution - coding silent 17:1653641-1653641 - ESO-683 COSM1263165 c.2639G>A p.R880H Substitution - Missense 17:1675968-1675968 - TCGA-BR-8360-01 COSM4064132 c.1492C>T p.R498C Substitution - Missense 17:1679124-1679124 - Pat_34_A COSM5851881 c.4725G>C p.Q1575H Substitution - Missense 17:1660492-1660492 - Au2 COSM5600291 c.5291C>T p.S1764F Substitution - Missense 17:1658611-1658611 - B89-4 COSM1749868 c.5928G>T p.W1976C Substitution - Missense 17:1655409-1655409 - TCGA-C5-A1BQ-01 COSM4842278 c.6353C>G p.S2118C Substitution - Missense 17:1653558-1653558 - TCGA-DK-A1A3-01 COSM417183 c.3577G>A p.E1193K Substitution - Missense 17:1673437-1673437 - SNU-175 COSM2738858 c.1649T>C p.V550A Substitution - Missense 17:1678832-1678832 - SH-4435 COSM5009690 c.891T>C p.N297N Substitution - coding silent 17:1681030-1681030 - 2492721 COSM2738859 c.1615C>T p.R539C Substitution - Missense 17:1678866-1678866 - TCGA-AX-A05Z-01 COSM975837 c.3075G>T p.T1025T Substitution - coding silent 17:1674666-1674666 - ESCC_112 COSM5639463 c.1693C>T p.R565W Substitution - Missense 17:1678788-1678788 - 3N49-VS-3T49 COSM4982858 c.1143G>T p.P381P Substitution - coding silent 17:1679755-1679755 - 8016583 COSM3387721 c.1788C>T p.Y596Y Substitution - coding silent 17:1678584-1678584 - TCGA-AP-A051-01 COSM975799 c.6048C>T p.I2016I Substitution - coding silent 17:1653956-1653956 - P100 COSM5009272 c.3281G>A p.R1094H Substitution - Missense 17:1674460-1674460 - B22 COSM1749873 c.1914C>T p.L638L Substitution - coding silent 17:1677635-1677635 - ESCC_117 COSM5640022 c.4498G>A p.G1500R Substitution - Missense 17:1661003-1661003 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.181368 17p13.3 607300 2423005|dbSNP|BC000579|A/G|coding|Ser256Ser|855|Validated; 2423005|dbSNP|BC064370|A/G|coding|Ile2214Val|6718|Validated

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer AAG - MultiAAMissense p.H1875_L1876delinsQ c.5625_5627delCTT 17 1559852 UCEC A C Missense p.L1340R c.4019T>G 17 1565203 STAD A C Missense p.L1872R c.5615T>G 17 1559946 PRAD A C Missense p.M1591R c.4772T>G 17 1563739 HNSC A C Missense p.Y1445D c.4333T>G 17 1564570 THCA A G 3-UTRSNV . c.7005+104T>C 17 1553995 CM A G Missense p.V1147A c.3440T>C 17 1577046 GBM A G Missense p.Y592H c.1774T>C 17 1581892 CM A G Synonymous p.L838L c.2512T>C 17 1579541 CM - A IntronicInsertion . c.1600-14dupT 17 1582190 STAD A T Missense p.L1051H c.3152T>A 17 1577883 BRCA A T Missense p.Y1028N c.3082T>A 17 1577953 STAD A T Missense p.Y2127N c.6379T>A 17 1555073 UCEC C A IntronicSNV . c.5376+3G>T 17 1561817 SCLC C A Missense p.A870S c.2608G>T 17 1579293 LUAD C A Missense p.D1592Y c.4774G>T 17 1563737 UCEC C A Missense p.D1650Y c.4948G>T 17 1562841 HNSC C A Missense p.D171Y c.511G>T 17 1585256 LUSC C A Missense p.G626V c.1877G>T 17 1580966 BRCA C A Missense p.Q1169H c.3507G>T 17 1576801 HNSC C A Missense p.Q1575H c.4725G>T 17 1563786 LUAD C A Missense p.Q1595H c.4785G>T 17 1563726 STAD C A Missense p.R1139L c.3416G>T 17 1577070 LUSC C A Missense p.R855L c.2564G>T 17 1579337 STAD C A Missense p.W293L c.878G>T 17 1584337 LUSC C A Nonsense p.E972* c.2914G>T 17 1578592 PRAD C A Synonymous p.P1540P c.4620G>T 17 1564010 CM C A Synonymous p.V1001V c.3003G>T 17 1578503 LUAD C G Missense p.A687P c.2059G>C 17 1580392 AML C G Missense p.G2051A c.6152G>C 17 1557146 NB C G Missense p.K536N c.1608G>C 17 1582167 HNSC C G Missense p.R998P c.2993G>C 17 1578513 OV C G Missense p.W430C c.1290G>C 17 1582704 LUSC C G Synonymous p.L456L c.1368G>C 17 1582626 HNSC C T 3-UTRSNV . c.7005+2G>A 17 1554097 BRCA C T Missense p.A1847T c.5539G>A 17 1560022 COREAD C T Missense p.A1847T c.5539G>A 17 1560022 UCEC C T Missense p.A98T c.292G>A 17 1585565 CM C T Missense p.D1592N c.4774G>A 17 1563737 HNSC C T Missense p.E1193K c.3577G>A 17 1576731 BLCA C T Missense p.E1395K c.4183G>A 17 1564924 CM C T Missense p.E1612K c.4834G>A 17 1563247 CM C T Missense p.E978K c.2932G>A 17 1578574 CM C T Missense p.G1750E c.5249G>A 17 1561947 AML C T Missense p.R1163Q c.3488G>A 17 1576820 COREAD C T Missense p.R1195H c.3584G>A 17 1576724 BRCA C T Missense p.R1414H c.4241G>A 17 1564662 COREAD C T Missense p.R1832H c.5495G>A 17 1561557 UCEC C T Missense p.R240H c.719G>A 17 1584919 STAD C T Missense p.R820H c.2459G>A 17 1579594 UCEC C T Missense p.R880H c.2639G>A 17 1579262 ESCA C T Missense p.S1722N c.5165G>A 17 1562031 UCEC C T Synonymous p.K882K c.2646G>A 17 1579255 COREAD C T Synonymous p.L456L c.1368G>A 17 1582626 HNSC C T Synonymous p.L546L c.1638G>A 17 1582137 BRCA C T Synonymous p.P212P c.636G>A 17 1585131 LGG C T Synonymous p.Q675Q c.2025G>A 17 1580426 PIA C T Synonymous p.R158R c.474G>A 17 1585293 CM C T Synonymous p.R686R c.2058G>A 17 1580393 CM C T Synonymous p.V1997V c.5991G>A 17 1557307 LGG G A 3-UTRSNV . c.7005+10C>T 17 1554089 CM G A Missense p.A1006V c.3017C>T 17 1578489 BRCA G A Missense p.A458V c.1373C>T 17 1582621 RCCC G A Missense p.H1586Y c.4756C>T 17 1563755 CM G A Missense p.L238F c.712C>T 17 1584926 LUAD G A Missense p.L885F c.2653C>T 17 1579248 RCCC G A Missense p.L999F c.2995C>T 17 1578511 MB G A Missense p.P133S c.397C>T 17 1585460 CM G A Missense p.P167S c.499C>T 17 1585268 CM G A Missense p.P1871L c.5612C>T 17 1559949 RCCC G A Missense p.P2133L c.6398C>T 17 1555054 CM G A Missense p.P324L c.971C>T 17 1584244 CM G A Missense p.P436L c.1307C>T 17 1582687 CM G A Missense p.P729L c.2186C>T 17 1580001 CM G A Missense p.R1141C c.3421C>T 17 1577065 LGG G A Missense p.R1532C c.4594C>T 17 1564036 CM G A Missense p.R1832C c.5494C>T 17 1561558 UCEC G A Missense p.R1949W c.5845C>T 17 1558786 CM G A Missense p.R548W c.1642C>T 17 1582133 UCEC G A Missense p.S127F c.380C>T 17 1585477 CM G A Missense p.S26L c.77C>T 17 1587789 CM G A Missense p.S26L c.77C>T 17 1587789 HNSC G A Missense p.T1488I c.4463C>T 17 1564332 BRCA G A Missense p.T2003I c.6008C>T 17 1557290 BRCA G A Missense p.T589M c.1766C>T 17 1581900 STAD G A Synonymous p.D1653D c.4959C>T 17 1562830 STAD G A Synonymous p.F1229F c.3687C>T 17 1576462 CM G A Synonymous p.F1684F c.5052C>T 17 1562737 CM G A Synonymous p.F1719F c.5157C>T 17 1562039 BLCA G A Synonymous p.F1902F c.5706C>T 17 1559773 CM G A Synonymous p.F616F c.1848C>T 17 1581818 BRCA G A Synonymous p.H561H c.1683C>T 17 1582092 CM G A Synonymous p.I1125I c.3375C>T 17 1577111 CM G A Synonymous p.I2090I c.6270C>T 17 1556935 HNSC G A Synonymous p.L1573L c.4719C>T 17 1563792 OV G A Synonymous p.L513L c.1539C>T 17 1582371 BLCA G A Synonymous p.N1023N c.3069C>T 17 1577966 CM G A Synonymous p.R1667R c.5001C>T 17 1562788 MB G A Synonymous p.R2045R c.6135C>T 17 1557163 LUAD G A Synonymous p.T2033T c.6099C>T 17 1557199 CM G A Synonymous p.Y1470Y c.4410C>T 17 1564385 CM G C Missense p.L288V c.862C>G 17 1584776 RCCC G C Missense p.L459V c.1375C>G 17 1582619 LUSC G - Frameshift p.F128Lfs*23 c.384delC 17 1585473 COREAD GG AA Missense p.P63S c.186_187delinsTT 17 1586909 CM G - IntronicDeletion . c.2872+23delC 17 1578891 ESCA GTAAGT - InFrameDeletion p.H1875_L1876delHL c.5624_5629delACTTAC 17 1559850 RCCC G T Missense p.P2186Q c.6557C>A 17 1554801 STAD G T Missense p.R82S c.244C>A 17 1586852 CM G T Synonymous p.R758R c.2272C>A 17 1579915 CM G T Synonymous p.T1208T c.3624C>A 17 1576684 BLCA T A Missense p.D196V c.587A>T 17 1585180 LUSC T A Missense p.N1543I c.4628A>T 17 1564002 RCCC T C IntronicSNV . c.4022+40A>G 17 1565160 STAD T C Missense p.E1235G c.3704A>G 17 1576445 HNSC T C Missense p.H1875R c.5624A>G 17 1559855 UCEC T C Missense p.I1664V c.4990A>G 17 1562799 CM T C Missense p.I1809V c.5425A>G 17 1561627 BRCA T C Missense p.K1838E c.5512A>G 17 1560049 PRAD T C Missense p.M2147V c.6439A>G 17 1555013 STAD T C Missense p.N1069D c.3205A>G 17 1577830 SCLC T C Missense p.N1069S c.3206A>G 17 1577829 GBM T C Missense p.T813A c.2437A>G 17 1579616 THCA T G Missense p.I70L c.208A>C 17 1586888 RCCC T G Missense p.I761L c.2281A>C 17 1579906 COREAD