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 9 86294747 86294747 + Missense_Mutation SNP C C G TCGA-P6-A5OH-01A-11D-A30A-10 TCGA-P6-A5OH-11A-01D-A30A-10 g.chr9:86294747C>G c.654G>C c.(652-654)ttG>ttC p.L218F BLCA 9 86281340 86281340 + Silent SNP C C A TCGA-FD-A43P-01A-31D-A23U-08 TCGA-FD-A43P-10A-01D-A23U-08 g.chr9:86281340C>A c.1257G>T c.(1255-1257)ctG>ctT p.L419L BLCA 9 86281346 86281346 + Missense_Mutation SNP C C T TCGA-FD-A43P-01A-31D-A23U-08 TCGA-FD-A43P-10A-01D-A23U-08 g.chr9:86281346C>T c.1251G>A c.(1249-1251)atG>atA p.M417I BLCA 9 86284123 86284123 + Nonsense_Mutation SNP G G A TCGA-DK-AA74-01A-11D-A391-08 TCGA-DK-AA74-10A-01D-A394-08 g.chr9:86284123G>A c.1225C>T c.(1225-1227)Cag>Tag p.Q409* BLCA 9 86284243 86284243 + Splice_Site SNP C C G TCGA-ZF-AA56-01A-31D-A391-08 TCGA-ZF-AA56-10A-01D-A394-08 g.chr9:86284243C>G c.e7-1 BLCA 9 86292828 86292828 + Missense_Mutation SNP C C T TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr9:86292828C>T c.919G>A c.(919-921)Gaa>Aaa p.E307K BLCA 9 86292877 86292877 + Splice_Site SNP C C T TCGA-ZF-AA52-01A-12D-A391-08 TCGA-ZF-AA52-10A-01D-A394-08 g.chr9:86292877C>T c.e6-1 BRCA 9 86278792 86278792 + Missense_Mutation SNP G G C TCGA-D8-A1JA-01A-11D-A13L-09 TCGA-D8-A1JA-10A-01W-A14R-09 g.chr9:86278792G>C c.1615C>G c.(1615-1617)Cag>Gag p.Q539E BRCA 9 86294875 86294875 + Nonsense_Mutation SNP G G A TCGA-D8-A1XQ-01A-11D-A14K-09 TCGA-D8-A1XQ-10A-01D-A14K-09 g.chr9:86294875G>A c.526C>T c.(526-528)Cag>Tag p.Q176* BRCA 9 86294885 86294885 + Silent SNP C C T TCGA-AO-A0J9-01A-11W-A050-09 TCGA-AO-A0J9-10A-01W-A055-09 g.chr9:86294885C>T c.516G>A c.(514-516)caG>caA p.Q172Q CESC 9 86276830 86276830 + Missense_Mutation SNP G G C TCGA-C5-A7CL-01A-11D-A32I-09 TCGA-C5-A7CL-10A-01D-A32I-09 g.chr9:86276830G>C c.1642C>G c.(1642-1644)Cag>Gag p.Q548E CESC 9 86292833 86292833 + Missense_Mutation SNP G G A TCGA-JX-A3Q0-01A-11D-A21Q-09 TCGA-JX-A3Q0-10A-01D-A21Q-09 g.chr9:86292833G>A c.914C>T c.(913-915)tCt>tTt p.S305F CESC 9 86294834 86294834 + Missense_Mutation SNP G G C TCGA-Q1-A73O-01A-11D-A32I-09 TCGA-Q1-A73O-10B-01D-A32I-09 g.chr9:86294834G>C c.567C>G c.(565-567)atC>atG p.I189M CESC 9 86297962 86297962 + Nonsense_Mutation SNP G G A TCGA-EA-A3HU-01A-11D-A20U-09 TCGA-EA-A3HU-10B-01D-A20U-09 g.chr9:86297962G>A c.352C>T c.(352-354)Cag>Tag p.Q118* CHOL 9 86297904 86297904 + Missense_Mutation SNP G G T TCGA-ZD-A8I3-01A-11D-A417-09 TCGA-ZD-A8I3-10A-01D-A41A-09 g.chr9:86297904G>T c.410C>A c.(409-411)tCt>tAt p.S137Y COAD 9 86276755 86276755 + Nonsense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr9:86276755C>A c.1717G>T c.(1717-1719)Gga>Tga p.G573* COAD 9 86276796 86276796 + Missense_Mutation SNP A A C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr9:86276796A>C c.1676T>G c.(1675-1677)tTt>tGt p.F559C COAD 9 86280030 86280030 + Missense_Mutation SNP A A G TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr9:86280030A>G c.1363T>C c.(1363-1365)Tca>Cca p.S455P COAD 9 86284098 86284098 + Splice_Site SNP A A G TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr9:86284098A>G c.e7+1 COAD 9 86284178 86284178 + Silent SNP C C A TCGA-AZ-6608-01A-11D-1835-10 TCGA-AZ-6608-11A-01D-1835-10 g.chr9:86284178C>A c.1170G>T c.(1168-1170)ctG>ctT p.L390L COAD 9 86292715 86292715 + Silent SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr9:86292715G>A c.1032C>T c.(1030-1032)ggC>ggT p.G344G COAD 9 86292718 86292718 + Silent SNP A A G TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr9:86292718A>G c.1029T>C c.(1027-1029)ggT>ggC p.G343G COAD 9 86292809 86292809 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr9:86292809C>T c.938G>A c.(937-939)cGt>cAt p.R313H COAD 9 86297907 86297907 + Missense_Mutation SNP T T G TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr9:86297907T>G c.407A>C c.(406-408)aAc>aCc p.N136T COAD 9 86300963 86300963 + Silent SNP A A G TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr9:86300963A>G c.288T>C c.(286-288)atT>atC p.I96I COAD 9 86301035 86301035 + Silent SNP A A G TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr9:86301035A>G c.216T>C c.(214-216)caT>caC p.H72H COAD 9 86322496 86322496 + Silent SNP C C T TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr9:86322496C>T c.99G>A c.(97-99)gaG>gaA p.E33E COADREAD 9 86276755 86276755 + Nonsense_Mutation SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr9:86276755C>A c.1717G>T c.(1717-1719)Gga>Tga p.G573* COADREAD 9 86276796 86276796 + Missense_Mutation SNP A A C TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr9:86276796A>C c.1676T>G c.(1675-1677)tTt>tGt p.F559C COADREAD 9 86280030 86280030 + Missense_Mutation SNP A A G TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr9:86280030A>G c.1363T>C c.(1363-1365)Tca>Cca p.S455P COADREAD 9 86284098 86284098 + Splice_Site SNP A A G TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr9:86284098A>G c.e7+1 COADREAD 9 86284178 86284178 + Silent SNP C C A TCGA-AZ-6608-01A-11D-1835-10 TCGA-AZ-6608-11A-01D-1835-10 g.chr9:86284178C>A c.1170G>T c.(1168-1170)ctG>ctT p.L390L COADREAD 9 86292715 86292715 + Silent SNP G G A TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr9:86292715G>A c.1032C>T c.(1030-1032)ggC>ggT p.G344G COADREAD 9 86292718 86292718 + Silent SNP A A G TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr9:86292718A>G c.1029T>C c.(1027-1029)ggT>ggC p.G343G COADREAD 9 86292809 86292809 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr9:86292809C>T c.938G>A c.(937-939)cGt>cAt p.R313H COADREAD 9 86297907 86297907 + Missense_Mutation SNP T T G TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr9:86297907T>G c.407A>C c.(406-408)aAc>aCc p.N136T COADREAD 9 86300963 86300963 + Silent SNP A A G TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr9:86300963A>G c.288T>C c.(286-288)atT>atC p.I96I COADREAD 9 86301035 86301035 + Silent SNP A A G TCGA-AA-3966-01A-01W-1073-09 TCGA-AA-3966-10A-01W-1073-09 g.chr9:86301035A>G c.216T>C c.(214-216)caT>caC p.H72H COADREAD 9 86322496 86322496 + Silent SNP C C T TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr9:86322496C>T c.99G>A c.(97-99)gaG>gaA p.E33E DLBC 9 86322427 86322427 + Missense_Mutation SNP G G C TCGA-RQ-A68N-01A-11D-A31X-10 TCGA-RQ-A68N-10A-01D-A31X-10 g.chr9:86322427G>C c.168C>G c.(166-168)agC>agG p.S56R ESCA 9 86294848 86294848 + Missense_Mutation SNP T T C TCGA-LN-A49V-01A-11D-A247-09 TCGA-LN-A49V-10A-01D-A247-09 g.chr9:86294848T>C c.553A>G c.(553-555)Atg>Gtg p.M185V GBMLGG 9 86284200 86284200 + Missense_Mutation SNP T T C TCGA-F6-A8O4-01A-11D-A36O-08 TCGA-F6-A8O4-10A-01D-A367-08 g.chr9:86284200T>C c.1148A>G c.(1147-1149)cAa>cGa p.Q383R GBMLGG 9 86294709 86294717 + In_Frame_Del DEL TTATTCAAC TTATTCAAC - TCGA-S9-A7IS-01A-11D-A34A-08 TCGA-S9-A7IS-10A-01D-A34A-08 g.chr9:86294709_86294717delTTATTCAAC c.684_692delGTTGAATAA c.(682-693)atgttgaataat>att p.228_231MLNN>I GBMLGG 9 86297963 86297963 + Silent SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:86297963A>G c.351T>C c.(349-351)gcT>gcC p.A117A HNSC 9 86276731 86276731 + Missense_Mutation SNP C C T TCGA-CV-6961-01A-21D-1912-08 TCGA-CV-6961-10A-01D-1912-08 g.chr9:86276731C>T c.1741G>A c.(1741-1743)Gaa>Aaa p.E581K HNSC 9 86322560 86322560 + Missense_Mutation SNP C C T TCGA-HD-7754-01A-11D-2078-08 TCGA-HD-7754-10A-01D-2078-08 g.chr9:86322560C>T c.35G>A c.(34-36)gGc>gAc p.G12D KICH 9 86322497 86322498 + Frame_Shift_Ins INS - - C TCGA-KL-8325-01A-11D-2310-10 TCGA-KL-8325-11A-01D-2310-10 g.chr9:86322497_86322498insC c.97_98insG c.(97-99)gagfs p.E33fs KICH 9 86322500 86322500 + Frame_Shift_Del DEL G G - TCGA-KL-8325-01A-11D-2310-10 TCGA-KL-8325-11A-01D-2310-10 g.chr9:86322500delG c.95delC c.(94-96)gcgfs p.A32fs KICH 9 86322501 86322501 + Frame_Shift_Del DEL G G - TCGA-KL-8325-01A-11D-2310-10 TCGA-KL-8325-11A-01D-2310-10 g.chr9:86322501delG c.94delC c.(94-96)ccgfs p.P32fs KICH 9 86322502 86322505 + Frame_Shift_Del DEL GGAG GGAG - TCGA-KL-8325-01A-11D-2310-10 TCGA-KL-8325-11A-01D-2310-10 g.chr9:86322502_86322505delGGAG c.90_93delCTCC c.(88-93)gcctccfs p.AS30fs KICH 9 86322503 86322506 + Frame_Shift_Del DEL GGAG GGAG - TCGA-KL-8325-01A-11D-2310-10 TCGA-KL-8325-11A-01D-2310-10 g.chr9:86322503_86322506delGGAG c.89_92delCTCC c.(88-93)gctcccfs p.AP30fs KIPAN 9 86276810 86276810 + Silent SNP G G C TCGA-B0-5693-01A-11D-1534-10 TCGA-B0-5693-11A-01D-1534-10 g.chr9:86276810G>C c.1662C>G c.(1660-1662)ctC>ctG p.L554L KIPAN 9 86279973 86279973 + Missense_Mutation SNP C C T TCGA-EU-5906-01A-11D-1669-08 TCGA-EU-5906-10A-01D-1669-08 g.chr9:86279973C>T c.1420G>A c.(1420-1422)Gca>Aca p.A474T KIPAN 9 86292725 86292725 + Missense_Mutation SNP G G T TCGA-BP-5181-01A-01D-1429-08 TCGA-BP-5181-11A-01D-1429-08 g.chr9:86292725G>T c.1022C>A c.(1021-1023)aCt>aAt p.T341N KIPAN 9 86322497 86322498 + Frame_Shift_Ins INS - - C TCGA-KL-8325-01A-11D-2310-10 TCGA-KL-8325-11A-01D-2310-10 g.chr9:86322497_86322498insC c.97_98insG c.(97-99)gagfs p.E33fs KIPAN 9 86322500 86322500 + Frame_Shift_Del DEL G G - TCGA-KL-8325-01A-11D-2310-10 TCGA-KL-8325-11A-01D-2310-10 g.chr9:86322500delG c.95delC c.(94-96)gcgfs p.A32fs KIPAN 9 86322501 86322501 + Frame_Shift_Del DEL G G - TCGA-KL-8325-01A-11D-2310-10 TCGA-KL-8325-11A-01D-2310-10 g.chr9:86322501delG c.94delC c.(94-96)ccgfs p.P32fs KIPAN 9 86322502 86322505 + Frame_Shift_Del DEL GGAG GGAG - TCGA-KL-8325-01A-11D-2310-10 TCGA-KL-8325-11A-01D-2310-10 g.chr9:86322502_86322505delGGAG c.90_93delCTCC c.(88-93)gcctccfs p.AS30fs KIPAN 9 86322503 86322506 + Frame_Shift_Del DEL GGAG GGAG - TCGA-KL-8325-01A-11D-2310-10 TCGA-KL-8325-11A-01D-2310-10 g.chr9:86322503_86322506delGGAG c.89_92delCTCC c.(88-93)gctcccfs p.AP30fs KIRC 9 86276810 86276810 + Silent SNP G G C TCGA-B0-5693-01A-11D-1534-10 TCGA-B0-5693-11A-01D-1534-10 g.chr9:86276810G>C c.1662C>G c.(1660-1662)ctC>ctG p.L554L KIRC 9 86279973 86279973 + Missense_Mutation SNP C C T TCGA-EU-5906-01A-11D-1669-08 TCGA-EU-5906-10A-01D-1669-08 g.chr9:86279973C>T c.1420G>A c.(1420-1422)Gca>Aca p.A474T KIRC 9 86292725 86292725 + Missense_Mutation SNP G G T TCGA-BP-5181-01A-01D-1429-08 TCGA-BP-5181-11A-01D-1429-08 g.chr9:86292725G>T c.1022C>A c.(1021-1023)aCt>aAt p.T341N LGG 9 86284200 86284200 + Missense_Mutation SNP T T C TCGA-F6-A8O4-01A-11D-A36O-08 TCGA-F6-A8O4-10A-01D-A367-08 g.chr9:86284200T>C c.1148A>G c.(1147-1149)cAa>cGa p.Q383R LGG 9 86294709 86294717 + In_Frame_Del DEL TTATTCAAC TTATTCAAC - TCGA-S9-A7IS-01A-11D-A34A-08 TCGA-S9-A7IS-10A-01D-A34A-08 g.chr9:86294709_86294717delTTATTCAAC c.684_692delGTTGAATAA c.(682-693)atgttgaataat>att p.228_231MLNN>I LGG 9 86297963 86297963 + Silent SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:86297963A>G c.351T>C c.(349-351)gcT>gcC p.A117A LIHC 9 86276838 86276838 + Missense_Mutation SNP A A G TCGA-DD-A39Z-01A-11D-A20W-10 TCGA-DD-A39Z-11A-21D-A20W-10 g.chr9:86276838A>G c.1634T>C c.(1633-1635)gTc>gCc p.V545A LIHC 9 86284174 86284174 + Missense_Mutation SNP G G T TCGA-LG-A6GG-01A-11D-A30V-10 TCGA-LG-A6GG-10A-01D-A30V-10 g.chr9:86284174G>T c.1174C>A c.(1174-1176)Caa>Aaa p.Q392K LIHC 9 86284243 86284243 + Splice_Site SNP C C T TCGA-DD-A39Y-01A-11D-A20W-10 TCGA-DD-A39Y-11A-11D-A20W-10 g.chr9:86284243C>T c.e7-1 LIHC 9 86297921 86297921 + Silent SNP T T C TCGA-KR-A7K7-01A-11D-A33K-10 TCGA-KR-A7K7-10A-01D-A33K-10 g.chr9:86297921T>C c.393A>G c.(391-393)tcA>tcG p.S131S LUAD 9 86276788 86276788 + Missense_Mutation SNP G G T TCGA-44-5645-01A-01D-1625-08 TCGA-44-5645-10A-01D-1625-08 g.chr9:86276788G>T c.1684C>A c.(1684-1686)Cgt>Agt p.R562S LUAD 9 86278912 86278912 + Nonsense_Mutation SNP C C A TCGA-73-4666-01A-01D-1265-08 TCGA-73-4666-11A-01D-1265-08 g.chr9:86278912C>A c.1495G>T c.(1495-1497)Gga>Tga p.G499* LUAD 9 86279969 86279970 + Frame_Shift_Ins INS - - T TCGA-05-5715-01A-01D-1625-08 TCGA-05-5715-10A-01D-1625-08 g.chr9:86279969_86279970insT c.1423_1424insA c.(1423-1425)acgfs p.T475fs LUAD 9 86284187 86284187 + Silent SNP G G A TCGA-44-6778-01A-11D-1855-08 TCGA-44-6778-10A-01D-1855-08 g.chr9:86284187G>A c.1161C>T c.(1159-1161)aaC>aaT p.N387N LUAD 9 86292810 86292810 + Missense_Mutation SNP G G A TCGA-50-6590-01A-12D-1855-08 TCGA-50-6590-11A-01D-1855-08 g.chr9:86292810G>A c.937C>T c.(937-939)Cgt>Tgt p.R313C LUAD 9 86293365 86293365 + Silent SNP T T A TCGA-50-5933-01A-11D-1753-08 TCGA-50-5933-11A-01D-1753-08 g.chr9:86293365T>A c.861A>T c.(859-861)gcA>gcT p.A287A LUAD 9 86293406 86293406 + Missense_Mutation SNP G G A TCGA-55-6975-01A-11D-1945-08 TCGA-55-6975-11A-01D-1945-08 g.chr9:86293406G>A c.820C>T c.(820-822)Cgc>Tgc p.R274C LUAD 9 86294696 86294696 + Missense_Mutation SNP C C T TCGA-91-7771-01A-11D-2167-08 TCGA-91-7771-10A-01D-2167-08 g.chr9:86294696C>T c.705G>A c.(703-705)atG>atA p.M235I LUSC 9 86278932 86278932 + Missense_Mutation SNP C C T TCGA-66-2783-01A-01D-1267-08 TCGA-66-2783-11A-01D-1267-08 g.chr9:86278932C>T c.1475G>A c.(1474-1476)gGa>gAa p.G492E LUSC 9 86293468 86293468 + Missense_Mutation SNP C C A TCGA-85-6561-01A-11D-1817-08 TCGA-85-6561-10A-01D-1817-08 g.chr9:86293468C>A c.758G>T c.(757-759)aGg>aTg p.R253M PAAD 9 86278795 86278795 + Missense_Mutation SNP G G T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:86278795G>T c.1612C>A c.(1612-1614)Cct>Act p.P538T PAAD 9 86293447 86293447 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:86293447C>A c.779G>T c.(778-780)aGc>aTc p.S260I PAAD 9 86293476 86293476 + Missense_Mutation SNP C C A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr9:86293476C>A c.750G>T c.(748-750)gaG>gaT p.E250D PRAD 9 86293369 86293369 + Missense_Mutation SNP G G A TCGA-EJ-5509-01A-01D-1576-08 TCGA-EJ-5509-10A-01D-1577-08 g.chr9:86293369G>A c.857C>T c.(856-858)gCt>gTt p.A286V PRAD 9 86293436 86293436 + Missense_Mutation SNP T T G TCGA-EJ-A6RC-01A-11D-A32B-08 TCGA-EJ-A6RC-10A-01D-A329-08 g.chr9:86293436T>G c.790A>C c.(790-792)Agc>Cgc p.S264R SKCM 9 86279949 86279949 + Missense_Mutation SNP G G A TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr9:86279949G>A c.1444C>T c.(1444-1446)Cca>Tca p.P482S SKCM 9 86281332 86281332 + Missense_Mutation SNP G G A TCGA-EE-A3AE-06A-11D-A196-08 TCGA-EE-A3AE-10A-01D-A198-08 g.chr9:86281332G>A c.1265C>T c.(1264-1266)cCc>cTc p.P422L SKCM 9 86281333 86281333 + Missense_Mutation SNP G G A TCGA-ER-A2NE-06A-21D-A196-08 TCGA-ER-A2NE-10A-01D-A198-08 g.chr9:86281333G>A c.1264C>T c.(1264-1266)Ccc>Tcc p.P422S SKCM 9 86284156 86284156 + Missense_Mutation SNP G G A TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr9:86284156G>A c.1192C>T c.(1192-1194)Ccc>Tcc p.P398S SKCM 9 86322554 86322554 + Frame_Shift_Del DEL T T - TCGA-EE-A29P-06A-11D-A197-08 TCGA-EE-A29P-10A-01D-A199-08 g.chr9:86322554delT c.41delA c.(40-42)cagfs p.Q14fs

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BOCA-FR 9 86277104 86277104 single base substitution A C intron_variant BRCA-EU 9 86270328 86270328 single base substitution G A downstream_gene_variant BRCA-EU 9 86270466 86270467 deletion of <=200bp TA - downstream_gene_variant BRCA-EU 9 86270848 86270848 deletion of <=200bp A - downstream_gene_variant BRCA-EU 9 86271327 86271327 single base substitution G C downstream_gene_variant BRCA-EU 9 86271877 86271877 deletion of <=200bp A - downstream_gene_variant BRCA-EU 9 86272195 86272195 single base substitution C A downstream_gene_variant BRCA-EU 9 86273177 86273177 single base substitution G A downstream_gene_variant BRCA-EU 9 86273317 86273317 single base substitution G A downstream_gene_variant BRCA-EU 9 86273647 86273647 single base substitution G C downstream_gene_variant BRCA-EU 9 86274312 86274312 single base substitution G A downstream_gene_variant BRCA-EU 9 86274487 86274487 single base substitution G C downstream_gene_variant BRCA-EU 9 86277683 86277683 single base substitution T C intron_variant BRCA-EU 9 86277801 86277817 deletion of <=200bp GCAACACGGTTGAAACC - intron_variant BRCA-EU 9 86279103 86279103 single base substitution G A intron_variant BRCA-EU 9 86279122 86279122 single base substitution G A intron_variant BRCA-EU 9 86281738 86281738 single base substitution G C exon_variant BRCA-EU 9 86281738 86281738 single base substitution G C intron_variant BRCA-EU 9 86281738 86281738 single base substitution G C upstream_gene_variant BRCA-EU 9 86282051 86282051 deletion of <=200bp A - exon_variant BRCA-EU 9 86282051 86282051 deletion of <=200bp A - intron_variant BRCA-EU 9 86282051 86282051 deletion of <=200bp A - upstream_gene_variant BRCA-EU 9 86282814 86282814 single base substitution G C exon_variant BRCA-EU 9 86282814 86282814 single base substitution G C intron_variant BRCA-EU 9 86282814 86282814 single base substitution G C upstream_gene_variant BRCA-EU 9 86282849 86282849 single base substitution G C exon_variant BRCA-EU 9 86282849 86282849 single base substitution G C intron_variant BRCA-EU 9 86282849 86282849 single base substitution G C upstream_gene_variant BRCA-EU 9 86283411 86283411 single base substitution G A exon_variant BRCA-EU 9 86283411 86283411 single base substitution G A intron_variant BRCA-EU 9 86283411 86283411 single base substitution G A upstream_gene_variant BRCA-EU 9 86283426 86283426 single base substitution C T exon_variant BRCA-EU 9 86283426 86283426 single base substitution C T intron_variant BRCA-EU 9 86283426 86283426 single base substitution C T upstream_gene_variant BRCA-EU 9 86283545 86283545 single base substitution C G exon_variant BRCA-EU 9 86283545 86283545 single base substitution C G intron_variant BRCA-EU 9 86283545 86283545 single base substitution C G upstream_gene_variant BRCA-EU 9 86285544 86285544 deletion of <=200bp G - intron_variant BRCA-EU 9 86285544 86285544 deletion of <=200bp G - upstream_gene_variant BRCA-EU 9 86286462 86286462 single base substitution T G intron_variant BRCA-EU 9 86286462 86286462 single base substitution T G upstream_gene_variant BRCA-EU 9 86287561 86287561 single base substitution C T intron_variant BRCA-EU 9 86287561 86287561 single base substitution C T upstream_gene_variant BRCA-EU 9 86288796 86288796 single base substitution A G downstream_gene_variant BRCA-EU 9 86288796 86288796 single base substitution A G intron_variant BRCA-EU 9 86288796 86288796 single base substitution A G upstream_gene_variant BRCA-EU 9 86291096 86291096 single base substitution G A downstream_gene_variant BRCA-EU 9 86291096 86291096 single base substitution G A intron_variant BRCA-EU 9 86292085 86292085 single base substitution A G downstream_gene_variant BRCA-EU 9 86292085 86292085 single base substitution A G intron_variant BRCA-EU 9 86293006 86293006 single base substitution G A intron_variant BRCA-EU 9 86296717 86296717 single base substitution G C intron_variant BRCA-EU 9 86296793 86296793 single base substitution C G intron_variant BRCA-EU 9 86296824 86296824 single base substitution G C intron_variant BRCA-EU 9 86296832 86296832 single base substitution G A intron_variant BRCA-EU 9 86297133 86297133 single base substitution G C intron_variant BRCA-EU 9 86298089 86298089 single base substitution A C intron_variant BRCA-EU 9 86298214 86298214 single base substitution C G intron_variant BRCA-EU 9 86298277 86298277 single base substitution G T intron_variant BRCA-EU 9 86298831 86298831 single base substitution G A intron_variant BRCA-EU 9 86299119 86299119 deletion of <=200bp T - intron_variant BRCA-EU 9 86299191 86299191 deletion of <=200bp C - intron_variant BRCA-EU 9 86299432 86299432 single base substitution C G intron_variant BRCA-EU 9 86300402 86300402 single base substitution G C intron_variant BRCA-EU 9 86301857 86301857 single base substitution A C intron_variant BRCA-EU 9 86301857 86301857 single base substitution A C upstream_gene_variant BRCA-EU 9 86303828 86303828 insertion of <=200bp - A intron_variant BRCA-EU 9 86303828 86303828 insertion of <=200bp - A upstream_gene_variant BRCA-EU 9 86305824 86305824 single base substitution G A intron_variant BRCA-EU 9 86305824 86305824 single base substitution G A upstream_gene_variant BRCA-EU 9 86308492 86308492 single base substitution T A intron_variant BRCA-EU 9 86308876 86308876 single base substitution C A intron_variant BRCA-EU 9 86310144 86310144 single base substitution C T intron_variant BRCA-EU 9 86312079 86312079 single base substitution A G intron_variant BRCA-EU 9 86312967 86312967 deletion of <=200bp A - intron_variant BRCA-EU 9 86314259 86314259 single base substitution T A intron_variant BRCA-EU 9 86315558 86315558 single base substitution G C intron_variant BRCA-EU 9 86315829 86315829 single base substitution T G intron_variant BRCA-EU 9 86316944 86316944 single base substitution G C intron_variant BRCA-EU 9 86317339 86317339 deletion of <=200bp T - intron_variant BRCA-EU 9 86319825 86319825 deletion of <=200bp A - intron_variant BRCA-EU 9 86320275 86320275 single base substitution C G intron_variant BRCA-EU 9 86321121 86321121 single base substitution G A intron_variant BRCA-EU 9 86323581 86323581 single base substitution G C upstream_gene_variant BRCA-EU 9 86326895 86326895 single base substitution T C upstream_gene_variant BRCA-FR 9 86272195 86272195 single base substitution C A downstream_gene_variant BRCA-FR 9 86282874 86282874 single base substitution C T exon_variant BRCA-FR 9 86282874 86282874 single base substitution C T intron_variant BRCA-FR 9 86282874 86282874 single base substitution C T upstream_gene_variant BRCA-FR 9 86283545 86283545 single base substitution C G exon_variant BRCA-FR 9 86283545 86283545 single base substitution C G intron_variant BRCA-FR 9 86283545 86283545 single base substitution C G upstream_gene_variant BRCA-FR 9 86292085 86292085 single base substitution A G downstream_gene_variant BRCA-FR 9 86292085 86292085 single base substitution A G intron_variant BRCA-FR 9 86298277 86298277 single base substitution G T intron_variant BRCA-FR 9 86316944 86316944 single base substitution G C intron_variant BRCA-KR 9 86322540 86322540 single base substitution C T missense_variant G19R 55G>A BRCA-KR 9 86322540 86322540 single base substitution C T upstream_gene_variant BRCA-UK 9 86270328 86270328 single base substitution G A downstream_gene_variant BRCA-UK 9 86297864 86297864 insertion of <=200bp - T intron_variant BRCA-UK 9 86297864 86297864 insertion of <=200bp - T splice_donor_variant BRCA-UK 9 86297917 86297917 single base substitution G C exon_variant BRCA-UK 9 86297917 86297917 single base substitution G C intron_variant BRCA-UK 9 86297917 86297917 single base substitution G C missense_variant P133A 397C>G BRCA-UK 9 86310874 86310874 single base substitution G C intron_variant BRCA-UK 9 86313122 86313122 single base substitution G C intron_variant BRCA-US 9 86278792 86278792 single base substitution G C missense_variant Q145E 433C>G BRCA-US 9 86278792 86278792 single base substitution G C missense_variant Q511E 1531C>G BRCA-US 9 86278792 86278792 single base substitution G C missense_variant Q539E 1615C>G BRCA-US 9 86278792 86278792 single base substitution G C splice_region_variant BRCA-US 9 86294875 86294875 single base substitution G A exon_variant BRCA-US 9 86294875 86294875 single base substitution G A intron_variant BRCA-US 9 86294875 86294875 single base substitution G A stop_gained Q176* 526C>T BRCA-US 9 86294885 86294885 single base substitution C T exon_variant BRCA-US 9 86294885 86294885 single base substitution C T intron_variant BRCA-US 9 86294885 86294885 single base substitution C T synonymous_variant Q172Q 516G>A BTCA-JP 9 86280115 86280115 single base substitution A G exon_variant BTCA-JP 9 86280115 86280115 single base substitution A G intron_variant BTCA-JP 9 86281522 86281522 deletion of <=200bp G - exon_variant BTCA-JP 9 86281522 86281522 deletion of <=200bp G - intron_variant BTCA-JP 9 86281522 86281522 deletion of <=200bp G - upstream_gene_variant BTCA-JP 9 86293540 86293540 deletion of <=200bp A - intron_variant CESC-US 9 86276830 86276830 single base substitution G C exon_variant CESC-US 9 86276830 86276830 single base substitution G C missense_variant Q154E 460C>G CESC-US 9 86276830 86276830 single base substitution G C missense_variant Q520E 1558C>G CESC-US 9 86276830 86276830 single base substitution G C missense_variant Q548E 1642C>G CESC-US 9 86292833 86292833 single base substitution G A exon_variant CESC-US 9 86292833 86292833 single base substitution G A missense_variant S102F 305C>T CESC-US 9 86292833 86292833 single base substitution G A missense_variant S305F 914C>T CESC-US 9 86294834 86294834 single base substitution G C exon_variant CESC-US 9 86294834 86294834 single base substitution G C intron_variant CESC-US 9 86294834 86294834 single base substitution G C missense_variant I189M 567C>G CESC-US 9 86297962 86297962 single base substitution G A exon_variant CESC-US 9 86297962 86297962 single base substitution G A intron_variant CESC-US 9 86297962 86297962 single base substitution G A stop_gained Q118* 352C>T CLLE-ES 9 86301220 86301220 single base substitution C G intron_variant CLLE-ES 9 86301220 86301220 single base substitution C G upstream_gene_variant CLLE-ES 9 86302139 86302139 single base substitution G T intron_variant CLLE-ES 9 86302139 86302139 single base substitution G T upstream_gene_variant COAD-US 9 86276796 86276796 single base substitution A C downstream_gene_variant COAD-US 9 86276796 86276796 single base substitution A C exon_variant COAD-US 9 86276796 86276796 single base substitution A C missense_variant F531C 1592T>G COAD-US 9 86276796 86276796 single base substitution A C missense_variant F559C 1676T>G COAD-US 9 86278913 86278913 single base substitution C T exon_variant COAD-US 9 86278913 86278913 single base substitution C T synonymous_variant S104S 312G>A COAD-US 9 86278913 86278913 single base substitution C T synonymous_variant S470S 1410G>A COAD-US 9 86278913 86278913 single base substitution C T synonymous_variant S498S 1494G>A COAD-US 9 86280030 86280030 single base substitution A G exon_variant COAD-US 9 86280030 86280030 single base substitution A G missense_variant S427P 1279T>C COAD-US 9 86280030 86280030 single base substitution A G missense_variant S455P 1363T>C COAD-US 9 86280030 86280030 single base substitution A G missense_variant S61P 181T>C COAD-US 9 86284098 86284098 single base substitution A G exon_variant COAD-US 9 86284098 86284098 single base substitution A G splice_donor_variant COAD-US 9 86284098 86284098 single base substitution A G upstream_gene_variant COAD-US 9 86292809 86292809 single base substitution C T exon_variant COAD-US 9 86292809 86292809 single base substitution C T missense_variant R110H 329G>A COAD-US 9 86292809 86292809 single base substitution C T missense_variant R313H 938G>A COAD-US 9 86294841 86294841 single base substitution A G exon_variant COAD-US 9 86294841 86294841 single base substitution A G intron_variant COAD-US 9 86294841 86294841 single base substitution A G missense_variant V187A 560T>C COAD-US 9 86322496 86322496 single base substitution C T synonymous_variant E33E 99G>A COAD-US 9 86322496 86322496 single base substitution C T synonymous_variant E7E 21G>A COCA-CN 9 86279948 86279948 single base substitution G A exon_variant COCA-CN 9 86279948 86279948 single base substitution G A missense_variant P454L 1361C>T COCA-CN 9 86279948 86279948 single base substitution G A missense_variant P482L 1445C>T COCA-CN 9 86279948 86279948 single base substitution G A missense_variant P88L 263C>T COCA-CN 9 86292591 86292591 single base substitution T C downstream_gene_variant COCA-CN 9 86292591 86292591 single base substitution T C intron_variant COCA-CN 9 86292810 86292810 single base substitution G A exon_variant COCA-CN 9 86292810 86292810 single base substitution G A missense_variant R110C 328C>T COCA-CN 9 86292810 86292810 single base substitution G A missense_variant R313C 937C>T COCA-CN 9 86297781 86297781 single base substitution T C intron_variant COCA-CN 9 86297783 86297783 single base substitution A T intron_variant COCA-CN 9 86297838 86297838 single base substitution C T intron_variant COCA-CN 9 86312563 86312563 single base substitution C A intron_variant COCA-CN 9 86312967 86312967 single base substitution A T intron_variant COCA-CN 9 86317703 86317703 single base substitution T G intron_variant EOPC-DE 9 86298868 86298868 single base substitution G A intron_variant EOPC-DE 9 86309930 86309930 single base substitution A G intron_variant ESAD-UK 9 86270226 86270226 single base substitution T C downstream_gene_variant ESAD-UK 9 86271055 86271055 single base substitution A C downstream_gene_variant ESAD-UK 9 86272010 86272010 single base substitution C T downstream_gene_variant ESAD-UK 9 86274171 86274171 single base substitution T A downstream_gene_variant ESAD-UK 9 86277396 86277396 single base substitution C A intron_variant ESAD-UK 9 86277478 86277478 single base substitution T C intron_variant ESAD-UK 9 86278074 86278074 single base substitution G C intron_variant ESAD-UK 9 86278148 86278148 single base substitution C G intron_variant ESAD-UK 9 86279879 86279879 single base substitution T C intron_variant ESAD-UK 9 86280093 86280093 single base substitution G C exon_variant ESAD-UK 9 86280093 86280093 single base substitution G C intron_variant ESAD-UK 9 86280999 86280999 single base substitution T G intron_variant ESAD-UK 9 86280999 86280999 single base substitution T G upstream_gene_variant ESAD-UK 9 86285823 86285823 single base substitution A G intron_variant ESAD-UK 9 86285823 86285823 single base substitution A G upstream_gene_variant ESAD-UK 9 86285946 86285946 single base substitution A G intron_variant ESAD-UK 9 86285946 86285946 single base substitution A G upstream_gene_variant ESAD-UK 9 86286018 86286018 single base substitution T G intron_variant ESAD-UK 9 86286018 86286018 single base substitution T G upstream_gene_variant ESAD-UK 9 86287657 86287657 single base substitution C T intron_variant ESAD-UK 9 86287657 86287657 single base substitution C T upstream_gene_variant ESAD-UK 9 86287864 86287864 single base substitution A C downstream_gene_variant ESAD-UK 9 86287864 86287864 single base substitution A C intron_variant ESAD-UK 9 86287864 86287864 single base substitution A C upstream_gene_variant ESAD-UK 9 86289763 86289763 single base substitution A T downstream_gene_variant ESAD-UK 9 86289763 86289763 single base substitution A T intron_variant ESAD-UK 9 86293315 86293315 single base substitution G T intron_variant ESAD-UK 9 86297050 86297050 single base substitution A T intron_variant ESAD-UK 9 86298094 86298094 single base substitution G A intron_variant ESAD-UK 9 86298097 86298097 single base substitution G A intron_variant ESAD-UK 9 86298675 86298675 single base substitution C T intron_variant ESAD-UK 9 86298892 86298892 single base substitution C T intron_variant ESAD-UK 9 86300708 86300708 single base substitution C G intron_variant ESAD-UK 9 86301369 86301369 single base substitution G A intron_variant ESAD-UK 9 86301369 86301369 single base substitution G A upstream_gene_variant ESAD-UK 9 86303379 86303379 deletion of <=200bp T - intron_variant ESAD-UK 9 86303379 86303379 deletion of <=200bp T - upstream_gene_variant ESAD-UK 9 86303500 86303500 single base substitution G A intron_variant ESAD-UK 9 86303500 86303500 single base substitution G A upstream_gene_variant ESAD-UK 9 86305857 86305857 single base substitution A T intron_variant ESAD-UK 9 86305857 86305857 single base substitution A T upstream_gene_variant ESAD-UK 9 86306114 86306114 insertion of <=200bp - AT intron_variant ESAD-UK 9 86306974 86306974 single base substitution C T intron_variant ESAD-UK 9 86311382 86311382 single base substitution T A intron_variant ESAD-UK 9 86314416 86314416 deletion of <=200bp T - intron_variant ESAD-UK 9 86314862 86314862 single base substitution C T intron_variant ESAD-UK 9 86316574 86316574 single base substitution A G intron_variant ESAD-UK 9 86321545 86321545 single base substitution C A intron_variant ESAD-UK 9 86323365 86323365 single base substitution C A upstream_gene_variant ESAD-UK 9 86323868 86323868 single base substitution G A upstream_gene_variant ESAD-UK 9 86326356 86326356 single base substitution A C upstream_gene_variant ESAD-UK 9 86326527 86326527 single base substitution T C upstream_gene_variant ESAD-UK 9 86327210 86327210 single base substitution A C upstream_gene_variant ESCA-CN 9 86293539 86293539 single base substitution G A intron_variant KIRC-US 9 86276810 86276810 single base substitution G C downstream_gene_variant KIRC-US 9 86276810 86276810 single base substitution G C exon_variant KIRC-US 9 86276810 86276810 single base substitution G C synonymous_variant L526L 1578C>G KIRC-US 9 86276810 86276810 single base substitution G C synonymous_variant L554L 1662C>G KIRC-US 9 86279973 86279973 single base substitution C T exon_variant KIRC-US 9 86279973 86279973 single base substitution C T missense_variant A446T 1336G>A KIRC-US 9 86279973 86279973 single base substitution C T missense_variant A474T 1420G>A KIRC-US 9 86279973 86279973 single base substitution C T missense_variant A80T 238G>A LAML-KR 9 86298204 86298204 single base substitution A G intron_variant LICA-FR 9 86270464 86270464 deletion of <=200bp T - downstream_gene_variant LICA-FR 9 86278442 86278442 single base substitution T C intron_variant LICA-FR 9 86294873 86294873 single base substitution C T exon_variant LICA-FR 9 86294873 86294873 single base substitution C T intron_variant LICA-FR 9 86294873 86294873 single base substitution C T synonymous_variant Q176Q 528G>A LICA-FR 9 86294918 86294918 single base substitution C T exon_variant LICA-FR 9 86294918 86294918 single base substitution C T intron_variant LICA-FR 9 86294918 86294918 single base substitution C T synonymous_variant L161L 483G>A LICA-FR 9 86327360 86327362 deletion of <=200bp TTT - upstream_gene_variant LIHC-US 9 86284174 86284174 single base substitution G T exon_variant LIHC-US 9 86284174 86284174 single base substitution G T missense_variant Q11K 31C>A LIHC-US 9 86284174 86284174 single base substitution G T missense_variant Q392K 1174C>A LIHC-US 9 86284174 86284174 single base substitution G T upstream_gene_variant LIHC-US 9 86297921 86297921 single base substitution T C exon_variant LIHC-US 9 86297921 86297921 single base substitution T C intron_variant LIHC-US 9 86297921 86297921 single base substitution T C synonymous_variant S131S 393A>G LINC-JP 9 86275817 86275817 single base substitution A G 3_prime_UTR_variant LINC-JP 9 86275817 86275817 single base substitution A G downstream_gene_variant LINC-JP 9 86275817 86275817 single base substitution A G exon_variant LINC-JP 9 86277496 86277496 single base substitution C A intron_variant LINC-JP 9 86284931 86284931 single base substitution T C intron_variant LINC-JP 9 86284931 86284931 single base substitution T C upstream_gene_variant LINC-JP 9 86292955 86292955 single base substitution G T intron_variant LINC-JP 9 86295246 86295246 single base substitution T C intron_variant LINC-JP 9 86297752 86297752 single base substitution A T intron_variant LINC-JP 9 86297754 86297754 single base substitution T A intron_variant LINC-JP 9 86301041 86301041 single base substitution T C intron_variant LINC-JP 9 86301041 86301041 single base substitution T C synonymous_variant K70K 210A>G LINC-JP 9 86301041 86301041 single base substitution T C upstream_gene_variant LINC-JP 9 86302637 86302637 single base substitution A G intron_variant LINC-JP 9 86302637 86302637 single base substitution A G upstream_gene_variant LINC-JP 9 86305081 86305081 single base substitution T A intron_variant LINC-JP 9 86305081 86305081 single base substitution T A upstream_gene_variant LINC-JP 9 86309968 86309968 single base substitution T C intron_variant LINC-JP 9 86310065 86310065 insertion of <=200bp - A intron_variant LIRI-JP 9 86270102 86270102 single base substitution T C downstream_gene_variant LIRI-JP 9 86270175 86270175 single base substitution G C downstream_gene_variant LIRI-JP 9 86270295 86270295 single base substitution T A downstream_gene_variant LIRI-JP 9 86271681 86271681 single base substitution T A downstream_gene_variant LIRI-JP 9 86271761 86271761 single base substitution T G downstream_gene_variant LIRI-JP 9 86271765 86271765 single base substitution T C downstream_gene_variant LIRI-JP 9 86274322 86274322 single base substitution T C downstream_gene_variant LIRI-JP 9 86275899 86275899 single base substitution T C 3_prime_UTR_variant LIRI-JP 9 86275899 86275899 single base substitution T C downstream_gene_variant LIRI-JP 9 86275899 86275899 single base substitution T C exon_variant LIRI-JP 9 86276447 86276447 deletion of <=200bp A - 3_prime_UTR_variant LIRI-JP 9 86276447 86276447 deletion of <=200bp A - downstream_gene_variant LIRI-JP 9 86276447 86276447 deletion of <=200bp A - exon_variant LIRI-JP 9 86276470 86276470 single base substitution T C 3_prime_UTR_variant LIRI-JP 9 86276470 86276470 single base substitution T C downstream_gene_variant LIRI-JP 9 86276470 86276470 single base substitution T C exon_variant LIRI-JP 9 86279562 86279562 single base substitution T A intron_variant LIRI-JP 9 86279946 86279946 single base substitution C T missense_variant G455R 1363G>A LIRI-JP 9 86279946 86279946 single base substitution C T missense_variant G483R 1447G>A LIRI-JP 9 86279946 86279946 single base substitution C T missense_variant G89R 265G>A LIRI-JP 9 86279946 86279946 single base substitution C T splice_region_variant LIRI-JP 9 86280359 86280359 single base substitution T C intron_variant LIRI-JP 9 86280359 86280359 single base substitution T C upstream_gene_variant LIRI-JP 9 86280699 86280699 single base substitution T C intron_variant LIRI-JP 9 86280699 86280699 single base substitution T C upstream_gene_variant LIRI-JP 9 86281131 86281131 single base substitution C G intron_variant LIRI-JP 9 86281131 86281131 single base substitution C G upstream_gene_variant LIRI-JP 9 86282406 86282406 single base substitution G C exon_variant LIRI-JP 9 86282406 86282406 single base substitution G C intron_variant LIRI-JP 9 86282406 86282406 single base substitution G C upstream_gene_variant LIRI-JP 9 86283032 86283032 single base substitution T C exon_variant LIRI-JP 9 86283032 86283032 single base substitution T C intron_variant LIRI-JP 9 86283032 86283032 single base substitution T C upstream_gene_variant LIRI-JP 9 86286268 86286268 single base substitution T G intron_variant LIRI-JP 9 86286268 86286268 single base substitution T G upstream_gene_variant LIRI-JP 9 86287394 86287394 single base substitution T C intron_variant LIRI-JP 9 86287394 86287394 single base substitution T C upstream_gene_variant LIRI-JP 9 86290314 86290314 single base substitution T C downstream_gene_variant LIRI-JP 9 86290314 86290314 single base substitution T C intron_variant LIRI-JP 9 86291064 86291064 single base substitution G T downstream_gene_variant LIRI-JP 9 86291064 86291064 single base substitution G T intron_variant LIRI-JP 9 86296571 86296571 single base substitution C A intron_variant LIRI-JP 9 86297156 86297156 single base substitution C T intron_variant LIRI-JP 9 86299238 86299238 single base substitution T C intron_variant LIRI-JP 9 86300461 86300461 single base substitution T C intron_variant LIRI-JP 9 86302938 86302938 single base substitution T C intron_variant LIRI-JP 9 86302938 86302938 single base substitution T C upstream_gene_variant LIRI-JP 9 86304768 86304768 single base substitution G C intron_variant LIRI-JP 9 86304768 86304768 single base substitution G C upstream_gene_variant LIRI-JP 9 86305773 86305773 single base substitution G A intron_variant LIRI-JP 9 86305773 86305773 single base substitution G A upstream_gene_variant LIRI-JP 9 86309225 86309225 single base substitution T C intron_variant LIRI-JP 9 86311829 86311829 single base substitution A T intron_variant LIRI-JP 9 86313262 86313262 single base substitution C A intron_variant LIRI-JP 9 86315851 86315851 single base substitution C G intron_variant LIRI-JP 9 86316971 86316971 single base substitution T C intron_variant LIRI-JP 9 86320683 86320683 single base substitution A G intron_variant LIRI-JP 9 86321173 86321173 single base substitution T C intron_variant LIRI-JP 9 86321559 86321559 single base substitution T C intron_variant LIRI-JP 9 86321745 86321745 single base substitution A G intron_variant LIRI-JP 9 86321843 86321843 single base substitution A C intron_variant LIRI-JP 9 86323140 86323140 single base substitution A G upstream_gene_variant LUSC-KR 9 86277567 86277567 single base substitution C A intron_variant LUSC-KR 9 86281522 86281522 single base substitution G C exon_variant LUSC-KR 9 86281522 86281522 single base substitution G C intron_variant LUSC-KR 9 86281522 86281522 single base substitution G C upstream_gene_variant LUSC-KR 9 86287888 86287888 single base substitution T A downstream_gene_variant LUSC-KR 9 86287888 86287888 single base substitution T A intron_variant LUSC-KR 9 86287888 86287888 single base substitution T A upstream_gene_variant LUSC-KR 9 86292918 86292918 single base substitution G T intron_variant LUSC-KR 9 86301281 86301281 single base substitution T A intron_variant LUSC-KR 9 86301281 86301281 single base substitution T A upstream_gene_variant LUSC-KR 9 86310402 86310402 single base substitution C A intron_variant LUSC-KR 9 86311039 86311039 single base substitution G C intron_variant LUSC-KR 9 86322986 86322986 single base substitution C T 5_prime_UTR_variant LUSC-KR 9 86322986 86322986 single base substitution C T upstream_gene_variant LUSC-KR 9 86323717 86323717 single base substitution A C upstream_gene_variant LUSC-KR 9 86327098 86327098 single base substitution T C upstream_gene_variant LUSC-US 9 86278932 86278932 single base substitution C T exon_variant LUSC-US 9 86278932 86278932 single base substitution C T missense_variant G464E 1391G>A LUSC-US 9 86278932 86278932 single base substitution C T missense_variant G492E 1475G>A LUSC-US 9 86278932 86278932 single base substitution C T missense_variant G98E 293G>A LUSC-US 9 86293468 86293468 single base substitution C A exon_variant LUSC-US 9 86293468 86293468 single base substitution C A missense_variant R253M 758G>T LUSC-US 9 86293468 86293468 single base substitution C A missense_variant R50M 149G>T MALY-DE 9 86273285 86273285 single base substitution C G downstream_gene_variant MALY-DE 9 86279356 86279356 single base substitution T C intron_variant MALY-DE 9 86280939 86280939 single base substitution G T intron_variant MALY-DE 9 86280939 86280939 single base substitution G T upstream_gene_variant MALY-DE 9 86288548 86288548 single base substitution A C downstream_gene_variant MALY-DE 9 86288548 86288548 single base substitution A C intron_variant MALY-DE 9 86288548 86288548 single base substitution A C upstream_gene_variant MALY-DE 9 86289687 86289687 single base substitution T A downstream_gene_variant MALY-DE 9 86289687 86289687 single base substitution T A intron_variant MALY-DE 9 86290487 86290487 single base substitution A G downstream_gene_variant MALY-DE 9 86290487 86290487 single base substitution A G intron_variant MALY-DE 9 86292877 86292877 single base substitution C A splice_acceptor_variant MALY-DE 9 86294881 86294881 single base substitution G A exon_variant MALY-DE 9 86294881 86294881 single base substitution G A intron_variant MALY-DE 9 86294881 86294881 single base substitution G A stop_gained Q174* 520C>T MALY-DE 9 86295759 86295759 single base substitution A C intron_variant MALY-DE 9 86297205 86297206 deletion of <=200bp AT - intron_variant MALY-DE 9 86297670 86297670 single base substitution G A intron_variant MALY-DE 9 86297892 86297892 single base substitution G A exon_variant MALY-DE 9 86297892 86297892 single base substitution G A intron_variant MALY-DE 9 86297892 86297892 single base substitution G A missense_variant S141F 422C>T MALY-DE 9 86306624 86306625 deletion of <=200bp GA - intron_variant MALY-DE 9 86306712 86306712 single base substitution T G intron_variant MALY-DE 9 86307480 86307480 single base substitution A G intron_variant MALY-DE 9 86308653 86308653 single base substitution A C intron_variant MALY-DE 9 86310982 86310982 single base substitution G T intron_variant MALY-DE 9 86314891 86314891 single base substitution T A intron_variant MALY-DE 9 86314954 86314954 single base substitution T C intron_variant MALY-DE 9 86315102 86315102 single base substitution T C intron_variant MALY-DE 9 86323149 86323149 single base substitution A G upstream_gene_variant MALY-DE 9 86323390 86323390 single base substitution C G upstream_gene_variant MALY-DE 9 86326364 86326364 single base substitution G C upstream_gene_variant MALY-DE 9 86326700 86326700 single base substitution C T upstream_gene_variant MALY-DE 9 86327442 86327442 single base substitution A C upstream_gene_variant MELA-AU 9 86270292 86270292 single base substitution G A downstream_gene_variant MELA-AU 9 86270466 86270466 single base substitution T A downstream_gene_variant MELA-AU 9 86271530 86271530 single base substitution G A downstream_gene_variant MELA-AU 9 86272875 86272875 single base substitution G A downstream_gene_variant MELA-AU 9 86274328 86274328 single base substitution G A downstream_gene_variant MELA-AU 9 86274677 86274677 single base substitution G A downstream_gene_variant MELA-AU 9 86275120 86275120 single base substitution G A 3_prime_UTR_variant MELA-AU 9 86275120 86275120 single base substitution G A downstream_gene_variant MELA-AU 9 86275120 86275120 single base substitution G A exon_variant MELA-AU 9 86276104 86276104 single base substitution G A 3_prime_UTR_variant MELA-AU 9 86276104 86276104 single base substitution G A downstream_gene_variant MELA-AU 9 86276104 86276104 single base substitution G A exon_variant MELA-AU 9 86276412 86276412 single base substitution G A 3_prime_UTR_variant MELA-AU 9 86276412 86276412 single base substitution G A downstream_gene_variant MELA-AU 9 86276412 86276412 single base substitution G A exon_variant MELA-AU 9 86276863 86276863 single base substitution G A intron_variant MELA-AU 9 86277790 86277790 single base substitution G T intron_variant MELA-AU 9 86278102 86278102 single base substitution G A intron_variant MELA-AU 9 86278431 86278431 single base substitution G A intron_variant MELA-AU 9 86278661 86278661 single base substitution T C intron_variant MELA-AU 9 86278774 86278774 single base substitution G A intron_variant MELA-AU 9 86279893 86279893 single base substitution T A intron_variant MELA-AU 9 86279960 86279960 single base substitution G A exon_variant MELA-AU 9 86279960 86279960 single base substitution G A missense_variant P450L 1349C>T MELA-AU 9 86279960 86279960 single base substitution G A missense_variant P478L 1433C>T MELA-AU 9 86279960 86279960 single base substitution G A missense_variant P84L 251C>T MELA-AU 9 86281058 86281058 single base substitution G A intron_variant MELA-AU 9 86281058 86281058 single base substitution G A upstream_gene_variant MELA-AU 9 86281897 86281897 single base substitution G A exon_variant MELA-AU 9 86281897 86281897 single base substitution G A intron_variant MELA-AU 9 86281897 86281897 single base substitution G A upstream_gene_variant MELA-AU 9 86283055 86283055 single base substitution A T exon_variant MELA-AU 9 86283055 86283055 single base substitution A T intron_variant MELA-AU 9 86283055 86283055 single base substitution A T upstream_gene_variant MELA-AU 9 86283537 86283537 single base substitution G A exon_variant MELA-AU 9 86283537 86283537 single base substitution G A intron_variant MELA-AU 9 86283537 86283537 single base substitution G A upstream_gene_variant MELA-AU 9 86285030 86285030 single base substitution G A intron_variant MELA-AU 9 86285030 86285030 single base substitution G A upstream_gene_variant MELA-AU 9 86286544 86286544 single base substitution A G intron_variant MELA-AU 9 86286544 86286544 single base substitution A G upstream_gene_variant MELA-AU 9 86286831 86286831 single base substitution G A intron_variant MELA-AU 9 86286831 86286831 single base substitution G A upstream_gene_variant MELA-AU 9 86288984 86288984 single base substitution G A downstream_gene_variant MELA-AU 9 86288984 86288984 single base substitution G A intron_variant MELA-AU 9 86288984 86288984 single base substitution G A upstream_gene_variant MELA-AU 9 86289178 86289178 single base substitution G A downstream_gene_variant MELA-AU 9 86289178 86289178 single base substitution G A intron_variant MELA-AU 9 86289178 86289178 single base substitution G A upstream_gene_variant MELA-AU 9 86289578 86289578 single base substitution G A downstream_gene_variant MELA-AU 9 86289578 86289578 single base substitution G A intron_variant MELA-AU 9 86290785 86290785 single base substitution A G downstream_gene_variant MELA-AU 9 86290785 86290785 single base substitution A G intron_variant MELA-AU 9 86292936 86292936 single base substitution A C intron_variant MELA-AU 9 86293822 86293822 single base substitution G A intron_variant MELA-AU 9 86294434 86294434 single base substitution G A intron_variant MELA-AU 9 86294455 86294455 single base substitution G T intron_variant MELA-AU 9 86294940 86294940 single base substitution C T exon_variant MELA-AU 9 86294940 86294940 single base substitution C T intron_variant MELA-AU 9 86294940 86294940 single base substitution C T missense_variant G154E 461G>A MELA-AU 9 86297205 86297205 insertion of <=200bp - AT intron_variant MELA-AU 9 86297398 86297398 single base substitution A G intron_variant MELA-AU 9 86298711 86298711 single base substitution G A intron_variant MELA-AU 9 86299022 86299022 single base substitution G A intron_variant MELA-AU 9 86299329 86299329 single base substitution G A intron_variant MELA-AU 9 86299574 86299574 single base substitution A T intron_variant MELA-AU 9 86301353 86301353 single base substitution G C intron_variant MELA-AU 9 86301353 86301353 single base substitution G C upstream_gene_variant MELA-AU 9 86301479 86301479 single base substitution C G intron_variant MELA-AU 9 86301479 86301479 single base substitution C G upstream_gene_variant MELA-AU 9 86302083 86302084 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 9 86302083 86302084 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 9 86302220 86302220 single base substitution A G intron_variant MELA-AU 9 86302220 86302220 single base substitution A G upstream_gene_variant MELA-AU 9 86302414 86302414 single base substitution G T intron_variant MELA-AU 9 86302414 86302414 single base substitution G T upstream_gene_variant MELA-AU 9 86302819 86302819 single base substitution C T intron_variant MELA-AU 9 86302819 86302819 single base substitution C T upstream_gene_variant MELA-AU 9 86303758 86303758 single base substitution G T intron_variant MELA-AU 9 86303758 86303758 single base substitution G T upstream_gene_variant MELA-AU 9 86305437 86305437 single base substitution C T intron_variant MELA-AU 9 86305437 86305437 single base substitution C T upstream_gene_variant MELA-AU 9 86305959 86305959 single base substitution A C intron_variant MELA-AU 9 86305959 86305959 single base substitution A C upstream_gene_variant MELA-AU 9 86307932 86307932 single base substitution G A intron_variant MELA-AU 9 86308047 86308047 single base substitution A G intron_variant MELA-AU 9 86308849 86308850 multiple base substitution (>=2bp and <=200bp) AC CT intron_variant MELA-AU 9 86308995 86308995 single base substitution C T intron_variant MELA-AU 9 86309301 86309301 single base substitution A T intron_variant MELA-AU 9 86309659 86309660 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 9 86309763 86309763 single base substitution C T intron_variant MELA-AU 9 86310113 86310113 single base substitution C T intron_variant MELA-AU 9 86310373 86310373 single base substitution G A intron_variant MELA-AU 9 86310441 86310441 single base substitution G A intron_variant MELA-AU 9 86311316 86311316 single base substitution C T intron_variant MELA-AU 9 86312715 86312715 single base substitution G A intron_variant MELA-AU 9 86313146 86313146 single base substitution G A intron_variant MELA-AU 9 86314009 86314009 single base substitution G A intron_variant MELA-AU 9 86315421 86315421 single base substitution T C intron_variant MELA-AU 9 86316581 86316581 single base substitution A G intron_variant MELA-AU 9 86316767 86316767 single base substitution A C intron_variant MELA-AU 9 86318592 86318592 single base substitution A G intron_variant MELA-AU 9 86318659 86318659 single base substitution A G intron_variant MELA-AU 9 86319329 86319329 single base substitution G A intron_variant MELA-AU 9 86319477 86319478 multiple base substitution (>=2bp and <=200bp) CA AT intron_variant MELA-AU 9 86319596 86319596 single base substitution C T intron_variant MELA-AU 9 86321311 86321311 single base substitution A G intron_variant MELA-AU 9 86321351 86321351 single base substitution G A intron_variant MELA-AU 9 86322937 86322937 single base substitution C G 5_prime_UTR_variant MELA-AU 9 86322937 86322937 single base substitution C G upstream_gene_variant MELA-AU 9 86325437 86325437 single base substitution C T upstream_gene_variant MELA-AU 9 86325545 86325545 single base substitution C T upstream_gene_variant MELA-AU 9 86326488 86326488 single base substitution C T upstream_gene_variant MELA-AU 9 86326666 86326666 single base substitution C T upstream_gene_variant MELA-AU 9 86327773 86327774 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 9 86328090 86328090 single base substitution C T upstream_gene_variant ORCA-IN 9 86297916 86297916 single base substitution G C exon_variant ORCA-IN 9 86297916 86297916 single base substitution G C intron_variant ORCA-IN 9 86297916 86297916 single base substitution G C missense_variant P133R 398C>G ORCA-IN 9 86327721 86327721 single base substitution C T upstream_gene_variant OV-AU 9 86271278 86271278 single base substitution G T downstream_gene_variant OV-AU 9 86297717 86297717 single base substitution A G intron_variant OV-AU 9 86308336 86308336 single base substitution G T intron_variant OV-AU 9 86311195 86311195 single base substitution C G intron_variant OV-AU 9 86314082 86314082 single base substitution G C intron_variant OV-AU 9 86318505 86318505 single base substitution C G intron_variant OV-AU 9 86319481 86319481 single base substitution C G intron_variant PACA-AU 9 86273654 86273654 insertion of <=200bp - A downstream_gene_variant PACA-AU 9 86279535 86279535 single base substitution C T intron_variant PACA-AU 9 86284805 86284805 single base substitution C T intron_variant PACA-AU 9 86284805 86284805 single base substitution C T upstream_gene_variant PACA-AU 9 86288544 86288544 single base substitution G C downstream_gene_variant PACA-AU 9 86288544 86288544 single base substitution G C intron_variant PACA-AU 9 86288544 86288544 single base substitution G C upstream_gene_variant PACA-AU 9 86298575 86298575 single base substitution G C intron_variant PACA-AU 9 86301532 86301532 single base substitution C T intron_variant PACA-AU 9 86301532 86301532 single base substitution C T upstream_gene_variant PACA-AU 9 86301870 86301870 single base substitution C G intron_variant PACA-AU 9 86301870 86301870 single base substitution C G upstream_gene_variant PACA-AU 9 86307311 86307311 single base substitution G A intron_variant PACA-AU 9 86315179 86315179 single base substitution A T intron_variant PACA-AU 9 86315523 86315523 single base substitution T C intron_variant PACA-AU 9 86315822 86315822 single base substitution G A intron_variant PACA-AU 9 86320572 86320572 deletion of <=200bp A - intron_variant PACA-AU 9 86321005 86321005 single base substitution G C intron_variant PACA-AU 9 86322396 86322396 single base substitution G C intron_variant PACA-AU 9 86322601 86322603 deletion of <=200bp GGC - 5_prime_UTR_variant PACA-AU 9 86322601 86322603 deletion of <=200bp GGC - upstream_gene_variant PACA-AU 9 86322618 86322618 single base substitution T G 5_prime_UTR_variant PACA-AU 9 86322618 86322618 single base substitution T G upstream_gene_variant PACA-AU 9 86323274 86323274 single base substitution C G upstream_gene_variant PACA-AU 9 86325175 86325175 single base substitution G A upstream_gene_variant PACA-AU 9 86327788 86327788 single base substitution G A upstream_gene_variant PACA-CA 9 86271246 86271246 single base substitution A T downstream_gene_variant PACA-CA 9 86272537 86272537 single base substitution T G downstream_gene_variant PACA-CA 9 86276611 86276611 single base substitution C T 3_prime_UTR_variant PACA-CA 9 86276611 86276611 single base substitution C T downstream_gene_variant PACA-CA 9 86276611 86276611 single base substitution C T exon_variant PACA-CA 9 86276629 86276629 single base substitution T A 3_prime_UTR_variant PACA-CA 9 86276629 86276629 single base substitution T A downstream_gene_variant PACA-CA 9 86276629 86276629 single base substitution T A exon_variant PACA-CA 9 86278239 86278239 single base substitution A G intron_variant PACA-CA 9 86282439 86282439 single base substitution T C exon_variant PACA-CA 9 86282439 86282439 single base substitution T C intron_variant PACA-CA 9 86282439 86282439 single base substitution T C upstream_gene_variant PACA-CA 9 86285534 86285534 single base substitution G T intron_variant PACA-CA 9 86285534 86285534 single base substitution G T upstream_gene_variant PACA-CA 9 86288531 86288532 deletion of <=200bp AA - downstream_gene_variant PACA-CA 9 86288531 86288532 deletion of <=200bp AA - intron_variant PACA-CA 9 86288531 86288532 deletion of <=200bp AA - upstream_gene_variant PACA-CA 9 86289033 86289033 deletion of <=200bp G - downstream_gene_variant PACA-CA 9 86289033 86289033 deletion of <=200bp G - intron_variant PACA-CA 9 86289033 86289033 deletion of <=200bp G - upstream_gene_variant PACA-CA 9 86291331 86291331 single base substitution A C downstream_gene_variant PACA-CA 9 86291331 86291331 single base substitution A C intron_variant PACA-CA 9 86292702 86292702 single base substitution T C exon_variant PACA-CA 9 86292702 86292702 single base substitution T C missense_variant T146A 436A>G PACA-CA 9 86292702 86292702 single base substitution T C missense_variant T349A 1045A>G PACA-CA 9 86293519 86293519 single base substitution G T splice_region_variant PACA-CA 9 86295701 86295701 single base substitution G A intron_variant PACA-CA 9 86298474 86298474 single base substitution A C intron_variant PACA-CA 9 86299193 86299193 single base substitution T C intron_variant PACA-CA 9 86299592 86299592 single base substitution G T intron_variant PACA-CA 9 86302285 86302285 single base substitution G C intron_variant PACA-CA 9 86302285 86302285 single base substitution G C upstream_gene_variant PACA-CA 9 86305624 86305624 single base substitution G A intron_variant PACA-CA 9 86305624 86305624 single base substitution G A upstream_gene_variant PACA-CA 9 86307763 86307763 single base substitution G A intron_variant PACA-CA 9 86309070 86309070 single base substitution T G intron_variant PACA-CA 9 86311382 86311382 single base substitution T A intron_variant PACA-CA 9 86316717 86316717 single base substitution C T intron_variant PACA-CA 9 86316842 86316842 single base substitution T C intron_variant PACA-CA 9 86319326 86319326 single base substitution G T intron_variant PACA-CA 9 86324705 86324705 single base substitution T A upstream_gene_variant PACA-CA 9 86325578 86325578 single base substitution G T upstream_gene_variant PACA-CA 9 86326002 86326002 single base substitution C G upstream_gene_variant PAEN-AU 9 86322061 86322061 single base substitution A C intron_variant PAEN-IT 9 86318208 86318208 single base substitution A G intron_variant PBCA-DE 9 86278115 86278115 deletion of <=200bp A - intron_variant PBCA-DE 9 86281326 86281326 single base substitution A G exon_variant PBCA-DE 9 86281326 86281326 single base substitution A G intron_variant PBCA-DE 9 86281326 86281326 single base substitution A G missense_variant F424S 1271T>C PBCA-DE 9 86281326 86281326 single base substitution A G upstream_gene_variant PBCA-DE 9 86287779 86287779 single base substitution C A downstream_gene_variant PBCA-DE 9 86287779 86287779 single base substitution C A intron_variant PBCA-DE 9 86287779 86287779 single base substitution C A upstream_gene_variant PBCA-DE 9 86287966 86287966 single base substitution G A downstream_gene_variant PBCA-DE 9 86287966 86287966 single base substitution G A intron_variant PBCA-DE 9 86287966 86287966 single base substitution G A upstream_gene_variant PBCA-DE 9 86293541 86293541 single base substitution A G intron_variant PBCA-DE 9 86297205 86297206 deletion of <=200bp AT - intron_variant PBCA-DE 9 86305851 86305851 single base substitution G A intron_variant PBCA-DE 9 86305851 86305851 single base substitution G A upstream_gene_variant PBCA-DE 9 86319657 86319657 single base substitution C T intron_variant PBCA-DE 9 86320965 86320965 single base substitution G T intron_variant PBCA-DE 9 86320966 86320966 single base substitution G A intron_variant PRAD-CA 9 86275772 86275772 single base substitution G A 3_prime_UTR_variant PRAD-CA 9 86275772 86275772 single base substitution G A downstream_gene_variant PRAD-CA 9 86275772 86275772 single base substitution G A exon_variant PRAD-CA 9 86294937 86294937 single base substitution A T exon_variant PRAD-CA 9 86294937 86294937 single base substitution A T intron_variant PRAD-CA 9 86294937 86294937 single base substitution A T missense_variant L155H 464T>A PRAD-CA 9 86305447 86305447 single base substitution T A intron_variant PRAD-CA 9 86305447 86305447 single base substitution T A upstream_gene_variant PRAD-UK 9 86272212 86272212 single base substitution G A downstream_gene_variant PRAD-UK 9 86276070 86276070 single base substitution T C 3_prime_UTR_variant PRAD-UK 9 86276070 86276070 single base substitution T C downstream_gene_variant PRAD-UK 9 86276070 86276070 single base substitution T C exon_variant PRAD-UK 9 86278507 86278507 insertion of <=200bp - A intron_variant PRAD-UK 9 86297055 86297055 deletion of <=200bp C - intron_variant PRAD-UK 9 86299659 86299659 single base substitution A C intron_variant PRAD-UK 9 86310279 86310279 single base substitution A C intron_variant PRAD-UK 9 86318229 86318229 single base substitution A G intron_variant PRAD-UK 9 86320010 86320010 single base substitution C T intron_variant PRAD-UK 9 86325163 86325163 single base substitution T G upstream_gene_variant PRAD-US 9 86293369 86293369 single base substitution G A exon_variant PRAD-US 9 86293369 86293369 single base substitution G A missense_variant A286V 857C>T PRAD-US 9 86293369 86293369 single base substitution G A missense_variant A83V 248C>T RECA-CN 9 86281297 86281297 single base substitution T C exon_variant RECA-CN 9 86281297 86281297 single base substitution T C intron_variant RECA-CN 9 86281297 86281297 single base substitution T C missense_variant M40V 118A>G RECA-CN 9 86281297 86281297 single base substitution T C missense_variant M434V 1300A>G RECA-CN 9 86281297 86281297 single base substitution T C upstream_gene_variant RECA-EU 9 86281220 86281220 single base substitution C T intron_variant RECA-EU 9 86281220 86281220 single base substitution C T upstream_gene_variant RECA-EU 9 86286178 86286178 single base substitution G C intron_variant RECA-EU 9 86286178 86286178 single base substitution G C upstream_gene_variant RECA-EU 9 86301776 86301776 single base substitution A T intron_variant RECA-EU 9 86301776 86301776 single base substitution A T upstream_gene_variant RECA-EU 9 86318796 86318796 single base substitution A T intron_variant RECA-EU 9 86320382 86320382 single base substitution C A intron_variant RECA-EU 9 86321176 86321176 single base substitution A C intron_variant SKCA-BR 9 86269949 86269949 single base substitution G A downstream_gene_variant SKCA-BR 9 86275580 86275580 single base substitution A C 3_prime_UTR_variant SKCA-BR 9 86275580 86275580 single base substitution A C downstream_gene_variant SKCA-BR 9 86275580 86275580 single base substitution A C exon_variant SKCA-BR 9 86277182 86277184 deletion of <=200bp TAC - intron_variant SKCA-BR 9 86277184 86277184 single base substitution C T intron_variant SKCA-BR 9 86277188 86277188 single base substitution T C intron_variant SKCA-BR 9 86277985 86277985 insertion of <=200bp - GAA intron_variant SKCA-BR 9 86279476 86279476 single base substitution G C intron_variant SKCA-BR 9 86281798 86281798 single base substitution T A exon_variant SKCA-BR 9 86281798 86281798 single base substitution T A intron_variant SKCA-BR 9 86281798 86281798 single base substitution T A upstream_gene_variant SKCA-BR 9 86284276 86284276 single base substitution G A intron_variant SKCA-BR 9 86284276 86284276 single base substitution G A upstream_gene_variant SKCA-BR 9 86286141 86286141 single base substitution G A intron_variant SKCA-BR 9 86286141 86286141 single base substitution G A upstream_gene_variant SKCA-BR 9 86287079 86287079 single base substitution G A intron_variant SKCA-BR 9 86287079 86287079 single base substitution G A upstream_gene_variant SKCA-BR 9 86288476 86288483 deletion of <=200bp AAAAAAAC - downstream_gene_variant SKCA-BR 9 86288476 86288483 deletion of <=200bp AAAAAAAC - intron_variant SKCA-BR 9 86288476 86288483 deletion of <=200bp AAAAAAAC - upstream_gene_variant SKCA-BR 9 86290448 86290448 single base substitution A C downstream_gene_variant SKCA-BR 9 86290448 86290448 single base substitution A C intron_variant SKCA-BR 9 86292181 86292182 deletion of <=200bp TA - downstream_gene_variant SKCA-BR 9 86292181 86292182 deletion of <=200bp TA - intron_variant SKCA-BR 9 86292938 86292938 insertion of <=200bp - CT intron_variant SKCA-BR 9 86293733 86293733 single base substitution A C intron_variant SKCA-BR 9 86295429 86295429 single base substitution G A intron_variant SKCA-BR 9 86295797 86295797 single base substitution G A intron_variant SKCA-BR 9 86305377 86305377 single base substitution T A intron_variant SKCA-BR 9 86305377 86305377 single base substitution T A upstream_gene_variant SKCA-BR 9 86312295 86312295 single base substitution G A intron_variant SKCA-BR 9 86312648 86312650 deletion of <=200bp CTT - intron_variant SKCA-BR 9 86314868 86314868 single base substitution C T intron_variant SKCA-BR 9 86316505 86316505 single base substitution T G intron_variant SKCA-BR 9 86324502 86324502 insertion of <=200bp - CGT upstream_gene_variant SKCA-BR 9 86327357 86327359 deletion of <=200bp TTC - upstream_gene_variant SKCM-US 9 86279949 86279949 single base substitution G A exon_variant SKCM-US 9 86279949 86279949 single base substitution G A missense_variant P454S 1360C>T SKCM-US 9 86279949 86279949 single base substitution G A missense_variant P482S 1444C>T SKCM-US 9 86279949 86279949 single base substitution G A missense_variant P88S 262C>T SKCM-US 9 86281332 86281332 single base substitution G A exon_variant SKCM-US 9 86281332 86281332 single base substitution G A intron_variant SKCM-US 9 86281332 86281332 single base substitution G A missense_variant P422L 1265C>T SKCM-US 9 86281332 86281332 single base substitution G A upstream_gene_variant SKCM-US 9 86281333 86281333 single base substitution G A exon_variant SKCM-US 9 86281333 86281333 single base substitution G A intron_variant SKCM-US 9 86281333 86281333 single base substitution G A missense_variant P422S 1264C>T SKCM-US 9 86281333 86281333 single base substitution G A upstream_gene_variant SKCM-US 9 86284156 86284156 single base substitution G A exon_variant SKCM-US 9 86284156 86284156 single base substitution G A missense_variant P17S 49C>T SKCM-US 9 86284156 86284156 single base substitution G A missense_variant P398S 1192C>T SKCM-US 9 86284156 86284156 single base substitution G A upstream_gene_variant SKCM-US 9 86300962 86300962 single base substitution G A exon_variant SKCM-US 9 86300962 86300962 single base substitution G A intron_variant SKCM-US 9 86300962 86300962 single base substitution G A missense_variant H97Y 289C>T SKCM-US 9 86322554 86322554 deletion of <=200bp T - frameshift_variant Q14 SKCM-US 9 86322554 86322554 deletion of <=200bp T - upstream_gene_variant STAD-US 9 86276735 86276735 single base substitution A C downstream_gene_variant STAD-US 9 86276735 86276735 single base substitution A C exon_variant STAD-US 9 86276735 86276735 single base substitution A C synonymous_variant A551A 1653T>G STAD-US 9 86276735 86276735 single base substitution A C synonymous_variant A579A 1737T>G STAD-US 9 86276800 86276800 single base substitution C T downstream_gene_variant STAD-US 9 86276800 86276800 single base substitution C T exon_variant STAD-US 9 86276800 86276800 single base substitution C T missense_variant G530R 1588G>A STAD-US 9 86276800 86276800 single base substitution C T missense_variant G558R 1672G>A STAD-US 9 86284162 86284164 deletion of <=200bp ACA - disruptive_inframe_deletion LS14S STAD-US 9 86284162 86284164 deletion of <=200bp ACA - disruptive_inframe_deletion LS395S STAD-US 9 86284162 86284164 deletion of <=200bp ACA - exon_variant STAD-US 9 86284162 86284164 deletion of <=200bp ACA - upstream_gene_variant STAD-US 9 86292640 86292640 single base substitution A G downstream_gene_variant STAD-US 9 86292640 86292640 single base substitution A G splice_donor_variant STAD-US 9 86292653 86292653 single base substitution G T downstream_gene_variant STAD-US 9 86292653 86292653 single base substitution G T exon_variant STAD-US 9 86292653 86292653 single base substitution G T missense_variant P365H 1094C>A STAD-US 9 86294735 86294735 single base substitution A T exon_variant STAD-US 9 86294735 86294735 single base substitution A T intron_variant STAD-US 9 86294735 86294735 single base substitution A T missense_variant N222K 666T>A THCA-SA 9 86275559 86275559 single base substitution C A 3_prime_UTR_variant THCA-SA 9 86275559 86275559 single base substitution C A downstream_gene_variant THCA-SA 9 86275559 86275559 single base substitution C A exon_variant THCA-SA 9 86278913 86278913 single base substitution C T exon_variant THCA-SA 9 86278913 86278913 single base substitution C T synonymous_variant S104S 312G>A THCA-SA 9 86278913 86278913 single base substitution C T synonymous_variant S470S 1410G>A THCA-SA 9 86278913 86278913 single base substitution C T synonymous_variant S498S 1494G>A THCA-SA 9 86284178 86284178 single base substitution C A exon_variant THCA-SA 9 86284178 86284178 single base substitution C A synonymous_variant L390L 1170G>T THCA-SA 9 86284178 86284178 single base substitution C A synonymous_variant L9L 27G>T THCA-SA 9 86284178 86284178 single base substitution C A upstream_gene_variant UCEC-US 9 86278894 86278894 single base substitution C T exon_variant UCEC-US 9 86278894 86278894 single base substitution C T missense_variant A111T 331G>A UCEC-US 9 86278894 86278894 single base substitution C T missense_variant A477T 1429G>A UCEC-US 9 86278894 86278894 single base substitution C T missense_variant A505T 1513G>A UCEC-US 9 86293456 86293456 single base substitution C T exon_variant UCEC-US 9 86293456 86293456 single base substitution C T missense_variant R257Q 770G>A UCEC-US 9 86293456 86293456 single base substitution C T missense_variant R54Q 161G>A UCEC-US 9 86294806 86294806 single base substitution G T exon_variant UCEC-US 9 86294806 86294806 single base substitution G T intron_variant UCEC-US 9 86294806 86294806 single base substitution G T missense_variant L199I 595C>A UCEC-US 9 86294871 86294871 single base substitution C T exon_variant UCEC-US 9 86294871 86294871 single base substitution C T intron_variant UCEC-US 9 86294871 86294871 single base substitution C T missense_variant R177Q 530G>A UCEC-US 9 86294875 86294875 single base substitution G A exon_variant UCEC-US 9 86294875 86294875 single base substitution G A intron_variant UCEC-US 9 86294875 86294875 single base substitution G A stop_gained Q176* 526C>T UCEC-US 9 86297895 86297895 single base substitution C T exon_variant UCEC-US 9 86297895 86297895 single base substitution C T intron_variant UCEC-US 9 86297895 86297895 single base substitution C T missense_variant G140D 419G>A UCEC-US 9 86322433 86322433 single base substitution C T synonymous_variant E28E 84G>A UCEC-US 9 86322433 86322433 single base substitution C T synonymous_variant E54E 162G>A

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand T7 COSM3764030 c.1494G>A p.S498S Substitution - coding silent 9:83663998-83663998 - T10 COSM5617737 c.883C>G p.P295A Substitution - Missense 9:83677949-83677949 - DLD1 COSM487611 c.1114T>C p.F372L Substitution - Missense 9:83669319-83669319 - TCGA-ER-A2NE-06 COSM3927119 c.1264C>T p.P422S Substitution - Missense 9:83666418-83666418 - TCGA-B2-5641-01 COSM487611 c.1114T>C p.F372L Substitution - Missense 9:83669319-83669319 - TCGA-LG-A6GG-01 COSM4939504 c.1174C>A p.Q392K Substitution - Missense 9:83669259-83669259 - TCGA-AU-6004-01 COSM1463295 c.1363T>C p.S455P Substitution - Missense 9:83665115-83665115 - TCGA-BG-A0MU-01 COSM1110597 c.1466G>A p.G489E Substitution - Missense 9:83664026-83664026 - TCGA-GN-A26C-01 COSM3659180 c.289C>T p.H97Y Substitution - Missense 9:83686047-83686047 - TCGA-AO-A0J9-01 COSM456162 c.516G>A p.Q172Q Substitution - coding silent 9:83679970-83679970 - TCGA-AA-3984-01 COSM297919 c.288T>C p.I96I Substitution - coding silent 9:83686048-83686048 - TCGA-B5-A11N-01 COSM1110604 c.162G>A p.E54E Substitution - coding silent 9:83707518-83707518 - S00829 COSM5660190 c.190G>A p.E64K Substitution - Missense 9:83686146-83686146 - TCGA-AM-5821-01 COSM3764030 c.1494G>A p.S498S Substitution - coding silent 9:83663998-83663998 - T368 COSM4738781 c.1535G>T p.S512I Substitution - Missense 9:83663957-83663957 - 587336 COSM1231594 c.820C>T p.R274C Substitution - Missense 9:83678491-83678491 - LUAD-B02594 COSM336974 c.445T>A p.L149I Substitution - Missense 9:83682954-83682954 - C135 COSM4611252 c.803delG p.G268fs*5 Deletion - Frameshift 9:83678508-83678508 - SC_9109 COSM5557995 c.103A>C p.K35Q Substitution - Missense 9:83707577-83707577 - TCGA-AZ-4315-01 COSM3699829 c.560T>C p.V187A Substitution - Missense 9:83679926-83679926 - PCSI_0090_Pa_X COSM3382588 c.1045A>G p.T349A Substitution - Missense 9:83677787-83677787 - CHC892T COSM4961280 c.528G>A p.Q176Q Substitution - coding silent 9:83679958-83679958 - 61 COSM5738639 c.1685G>A p.R562H Substitution - Missense 9:83661872-83661872 - CRC-03T COSM609513 c.937C>T p.R313C Substitution - Missense 9:83677895-83677895 - sysucc-1317T COSM5450599 c.1445C>T p.P482L Substitution - Missense 9:83665033-83665033 - CHC892T COSM4959345 c.483G>A p.L161L Substitution - coding silent 9:83680003-83680003 - T3021 COSM4738782 c.1185G>A p.L395L Substitution - coding silent 9:83669248-83669248 - CHC892T COSM4959345 c.483G>A p.L161L Substitution - coding silent 9:83680003-83680003 - TCGA-AP-A056-01 COSM1110601 c.530G>A p.R177Q Substitution - Missense 9:83679956-83679956 - TCGA-BP-5181-01 COSM1497119 c.1022C>A p.T341N Substitution - Missense 9:83677810-83677810 - TCGA-B0-5693-01 COSM487609 c.1662C>G p.L554L Substitution - coding silent 9:83661895-83661895 - RK082_C01 COSM1636263 c.1447G>A p.G483R Substitution - Missense 9:83665031-83665031 - TCGA-Q1-A73O-01 COSM4835246 c.567C>G p.I189M Substitution - Missense 9:83679919-83679919 - TCGA-BR-8382-01 COSM3908515 c.1094C>A p.P365H Substitution - Missense 9:83677738-83677738 - TCGA-AA-A010-01 COSM286248 c.1717G>T p.G573* Substitution - Nonsense 9:83661840-83661840 - TCGA-CA-6717-01 COSM1463294 c.1676T>G p.F559C Substitution - Missense 9:83661881-83661881 - TCGA-BS-A0UV-01 COSM1110599 c.770G>A p.R257Q Substitution - Missense 9:83678541-83678541 - KPOPBR-03-T COSM5965786 c.55G>A p.G19R Substitution - Missense 9:83707625-83707625 - T578 COSM4738784 c.789A>C p.E263D Substitution - Missense 9:83678522-83678522 - PD4132a COSM165377 c.397C>G p.P133A Substitution - Missense 9:83683002-83683002 - HCC82T COSM3664447 c.210A>G p.K70K Substitution - coding silent 9:83686126-83686126 - T10 COSM5617738 c.838C>G p.Q280E Substitution - Missense 9:83678473-83678473 - TCGA-AA-3966-01 COSM297214 c.216T>C p.H72H Substitution - coding silent 9:83686120-83686120 - TCGA-AA-3672-01 COSM267716 c.1029T>C p.G343G Substitution - coding silent 9:83677803-83677803 - TCGA-BR-6452-01 COSM3908516 c.666T>A p.N222K Substitution - Missense 9:83679820-83679820 - Pat_41_B COSM5876493 c.368C>T p.A123V Substitution - Missense 9:83683031-83683031 - CSCC-4-T COSM4524843 c.1294G>A p.E432K Substitution - Missense 9:83666388-83666388 - TCGA-BR-4184-01 COSM3908513 c.1672G>A p.G558R Substitution - Missense 9:83661885-83661885 - Pat_76_A COSM5876491 c.1342C>T p.P448S Substitution - Missense 9:83665136-83665136 - TCGA-D8-A1JA-01 COSM3848970 c.1615C>G p.Q539E Substitution - Missense 9:83663877-83663877 - HCC82 COSM3664447 c.210A>G p.K70K Substitution - coding silent 9:83686126-83686126 - 587342 COSM1231595 c.1447G>T p.G483W Substitution - Missense 9:83665031-83665031 - YUBER COSM1701263 c.638C>T p.P213L Substitution - Missense 9:83679848-83679848 - TCGA-AP-A051-01 COSM1110600 c.595C>A p.L199I Substitution - Missense 9:83679891-83679891 - TCGA-EU-5906-01 COSM487610 c.1420G>A p.A474T Substitution - Missense 9:83665058-83665058 - TCGA-AP-A059-01 COSM1110602 c.526C>T p.Q176* Substitution - Nonsense 9:83679960-83679960 - Sample_1 COSM3764030 c.1494G>A p.S498S Substitution - coding silent 9:83663998-83663998 - TCGA-AP-A056-01 COSM1110603 c.419G>A p.G140D Substitution - Missense 9:83682980-83682980 - TCGA-C5-A7CL-01 COSM4837922 c.1642C>G p.Q548E Substitution - Missense 9:83661915-83661915 - CHC892T COSM4961280 c.528G>A p.Q176Q Substitution - coding silent 9:83679958-83679958 - Pat_34_A COSM5876492 c.484G>A p.G162S Substitution - Missense 9:83680002-83680002 - HCT8 COSM487611 c.1114T>C p.F372L Substitution - Missense 9:83669319-83669319 - LC_C20 COSM1187748 c.965A>G p.N322S Substitution - Missense 9:83677867-83677867 - TCGA-85-6561-01 COSM754018 c.758G>T p.R253M Substitution - Missense 9:83678553-83678553 - MO_1124 COSM5568016 c.903C>T p.S301S Substitution - coding silent 9:83677929-83677929 - PCSI_0504_Pa_P_526 COSM4806648 c.712-5C>A p.? Unknown 9:83678604-83678604 - NB-1977 COSM1288803 c.1273G>T p.A425S Substitution - Missense 9:83666409-83666409 - HCC2998 COSM4631887 c.35G>A p.G12D Substitution - Missense 9:83707645-83707645 - CPCG_0183_Pr_P_P3 COSM3396765 c.480C>T p.S160S Substitution - coding silent 9:83680006-83680006 - CPCG0094-F1 COSM4879806 c.464T>A p.L155H Substitution - Missense 9:83680022-83680022 - 49M COSM5593820 c.962C>T p.P321L Substitution - Missense 9:83677870-83677870 - CSCC-16-T COSM4469674 c.1613C>T p.P538L Substitution - Missense 9:83663879-83663879 - TCGA-BR-6452-01 COSM3908512 c.1737T>G p.A579A Substitution - coding silent 9:83661820-83661820 - T3024 COSM4738783 c.821G>A p.R274H Substitution - Missense 9:83678490-83678490 - 61 COSM5738640 c.1209G>A p.M403I Substitution - Missense 9:83669224-83669224 - T10 COSM4407254 c.1590G>T p.L530L Substitution - coding silent 9:83663902-83663902 - TCGA-D5-6930-01 COSM1463299 c.99G>A p.E33E Substitution - coding silent 9:83707581-83707581 - HCT-15 COSM487611 c.1114T>C p.F372L Substitution - Missense 9:83669319-83669319 - tumor_4163639 COSM1161791 c.520C>T p.Q174* Substitution - Nonsense 9:83679966-83679966 - TCGA-GN-A266-06 COSM3659179 c.1192C>T p.P398S Substitution - Missense 9:83669241-83669241 - HCT15 COSM487611 c.1114T>C p.F372L Substitution - Missense 9:83669319-83669319 - TCGA-66-2783-01 COSM754019 c.1475G>A p.G492E Substitution - Missense 9:83664017-83664017 - Gp5D COSM3220213 c.52G>A p.A18T Substitution - Missense 9:83707628-83707628 - pfg122T COSM4758423 c.1493C>T p.S498L Substitution - Missense 9:83663999-83663999 - PT33 COSM5908962 c.1573T>C p.F525L Substitution - Missense 9:83663919-83663919 - 587238 COSM1231593 c.250A>T p.I84F Substitution - Missense 9:83686086-83686086 - SJACT02_D COSM4968329 c.914C>A p.S305Y Substitution - Missense 9:83677918-83677918 - K20-Tumor COSM249267 c.1300A>G p.M434V Substitution - Missense 9:83666382-83666382 - TCGA-CA-6717-01 COSM1463298 c.938G>A p.R313H Substitution - Missense 9:83677894-83677894 - TBR01 COSM4168244 c.319A>G p.K107E Substitution - Missense 9:83686017-83686017 - TCGA-CG-5721-01 COSM3908514 c.1105+2T>C p.? Unknown 9:83677725-83677725 - TCGA-D8-A1XQ-01 COSM1110602 c.526C>T p.Q176* Substitution - Nonsense 9:83679960-83679960 - PD4112a COSM166264 c.448+2_448+3insA p.? Unknown 9:83682948-83682949 - tumor_4124542 COSM5947204 c.871-1G>T p.? Unknown 9:83677962-83677962 - TCGA-BS-A0UF-01 COSM1110596 c.1513G>A p.A505T Substitution - Missense 9:83663979-83663979 - TCGA-EJ-5509-01 COSM1132443 c.857C>T p.A286V Substitution - Missense 9:83678454-83678454 - TCGA-KR-A7K7-01 COSM4922811 c.393A>G p.S131S Substitution - coding silent 9:83683006-83683006 - TCGA-D1-A177-01 COSM1110598 c.1183T>C p.L395L Substitution - coding silent 9:83669250-83669250 - TCGA-AA-A010-01 COSM286249 c.407A>C p.N136T Substitution - Missense 9:83682992-83682992 - TCGA-CM-6171-01 COSM1463296 c.1248+2T>C p.? Unknown 9:83669183-83669183 - TCGA-EE-A29D-06 COSM3659177 c.1444C>T p.P482S Substitution - Missense 9:83665034-83665034 - K20 COSM249267 c.1300A>G p.M434V Substitution - Missense 9:83666382-83666382 - TCGA-EE-A3AE-06 COSM3659178 c.1265C>T p.P422L Substitution - Missense 9:83666417-83666417 - CHC205T COSM4407254 c.1590G>T p.L530L Substitution - coding silent 9:83663902-83663902 - TCGA-JX-A3Q0-01 COSM4824409 c.914C>T p.S305F Substitution - Missense 9:83677918-83677918 - OSCC-GB_01070111 COSM4889373 c.398C>G p.P133R Substitution - Missense 9:83683001-83683001 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.9589 9q22|9q21.2-q21.3 605046 2406673|CGAP|BC010066|A/G|non-coding||2065|Candidate; 2406673|CGAP|BC039294|A/G|non-coding||2160|Candidate; 2406674|CGAP|BC010066|C/G|non-coding||2232|Candidate; 2406674|CGAP|BC039294|C/G|non-coding||2327|Candidate; 2406675|CGAP|BC010066|C/G|non-coding||108|Validated; 2406675|CGAP|BC039294|C/G|non-coding||119|Validated; 2406676|CGAP|BC010066|A/C|non-coding||98|Candidate; 2406676|CGAP|BC039294|A/C|non-coding||109|Candidate

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer C A Missense p.A425S c.1273G>T 9 86281324 NB C A Missense p.R253M c.758G>T 9 86293468 LUSC C A Nonsense p.E476* c.1426G>T 9 86279967 STAD C A Nonsense p.G499* c.1495G>T 9 86278912 LUAD CCTGAGTTGTTAAAAGCATACCTCCTACT - SpliceDonorDeletion . c.1098_1105+21delAGTAGGAGGTATGCTTTTAACAACTCAGG 9 86292621 BRCA C T Missense p.A474T c.1420G>A 9 86279973 RCCC C T Missense p.E581K c.1741G>A 9 86276731 HNSC C T Missense p.G12D c.35G>A 9 86322560 HNSC C T Missense p.G492E c.1475G>A 9 86278932 LUSC C T Synonymous p.Q172Q c.516G>A 9 86294885 BRCA G A Missense p.H97Y c.289C>T 9 86300962 CM G A Missense p.P422L c.1265C>T 9 86281332 CM G A Missense p.P422S c.1264C>T 9 86281333 CM G A Missense p.R313C c.937C>T 9 86292810 LUAD G A Nonsense p.Q174* c.520C>T 9 86294881 DLBCL G A Synonymous p.N387N c.1161C>T 9 86284187 LUAD G C Missense p.P133A c.397C>G 9 86297917 BRCA G C Synonymous p.L554L c.1662C>G 9 86276810 RCCC G T Missense p.R562S c.1684C>A 9 86276788 LUAD T A Synonymous p.A287A c.861A>T 9 86293365 LUAD T C 3-UTRSNV . c.1767+235A>G 9 86276470 HC T C 3-UTRSNV . c.1767+806A>G 9 86275899 HC T C IntronicSNV . c.1248+1068A>G 9 86283032 HC T C Missense p.K107E c.319A>G 9 86300932 ALL T - Frameshift p.Q14Rfs*24 c.41delA 9 86322554 CM - T Frameshift p.T475Nfs*27 c.1423dupA 9 86279970 LUAD - T SpliceDonorInsertion . c.448_448+1insA 9 86297865 BRCA