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 4 164050138 164050138 + Missense_Mutation SNP A A G TCGA-PK-A5HB-01A-11D-A29I-10 TCGA-PK-A5HB-11A-11D-A29L-10 g.chr4:164050138A>G c.1396T>C c.(1396-1398)Tac>Cac p.Y466H ACC 4 164050186 164050186 + Missense_Mutation SNP C C T TCGA-OR-A5K8-01A-11D-A29I-10 TCGA-OR-A5K8-10A-01D-A29L-10 g.chr4:164050186C>T c.1348G>A c.(1348-1350)Ggt>Agt p.G450S BLCA 4 164050300 164050300 + Missense_Mutation SNP G G C TCGA-DK-A2I1-01A-11D-A17V-08 TCGA-DK-A2I1-10A-01D-A17V-08 g.chr4:164050300G>C c.1234C>G c.(1234-1236)Cag>Gag p.Q412E BLCA 4 164054328 164054328 + Silent SNP G G C TCGA-G2-AA3B-01A-11D-A391-08 TCGA-G2-AA3B-10A-01D-A394-08 g.chr4:164054328G>C c.1011C>G c.(1009-1011)ctC>ctG p.L337L BLCA 4 164087527 164087527 + Missense_Mutation SNP G G A TCGA-DK-AA75-01A-11D-A391-08 TCGA-DK-AA75-10A-01D-A394-08 g.chr4:164087527G>A c.353C>T c.(352-354)tCg>tTg p.S118L BLCA 4 164087539 164087539 + Missense_Mutation SNP G G A TCGA-DK-A1AC-01A-11D-A13W-08 TCGA-DK-A1AC-10A-01D-A13W-08 g.chr4:164087539G>A c.341C>T c.(340-342)tCg>tTg p.S114L BLCA 4 164087786 164087786 + Missense_Mutation SNP G G C TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr4:164087786G>C c.94C>G c.(94-96)Ccg>Gcg p.P32A BRCA 4 164061489 164061489 + Missense_Mutation SNP C C T TCGA-HN-A2NL-01A-11D-A18P-09 TCGA-HN-A2NL-10A-01D-A18P-09 g.chr4:164061489C>T c.764G>A c.(763-765)cGg>cAg p.R255Q BRCA 4 164085408 164085408 + Missense_Mutation SNP C C G TCGA-AC-A3W7-01A-11D-A228-09 TCGA-AC-A3W7-10A-01D-A22A-09 g.chr4:164085408C>G c.501G>C c.(499-501)aaG>aaC p.K167N CESC 4 164048226 164048226 + IGR SNP G G T TCGA-LP-A4AW-01A-11D-A243-09 TCGA-LP-A4AW-10A-01D-A243-09 g.chr4:164048226G>T CESC 4 164069547 164069547 + Missense_Mutation SNP C C T TCGA-IR-A3LA-01A-11D-A22X-09 TCGA-IR-A3LA-10A-01D-A22X-09 g.chr4:164069547C>T c.580G>A c.(580-582)Gaa>Aaa p.E194K CESC 4 164085493 164085493 + Missense_Mutation SNP G G A TCGA-IR-A3LH-01A-21D-A20U-09 TCGA-IR-A3LH-10A-01D-A20U-09 g.chr4:164085493G>A c.416C>T c.(415-417)tCa>tTa p.S139L CHOL 4 164050118 164050118 + Silent SNP A A G TCGA-W5-AA31-01A-11D-A417-09 TCGA-W5-AA31-10A-01D-A41A-09 g.chr4:164050118A>G c.1416T>C c.(1414-1416)ccT>ccC p.P472P CHOL 4 164050124 164050124 + Silent SNP T T G TCGA-W5-AA31-01A-11D-A417-09 TCGA-W5-AA31-10A-01D-A41A-09 g.chr4:164050124T>G c.1410A>C c.(1408-1410)ccA>ccC p.P470P CHOL 4 164050124 164050124 + Silent SNP T T G TCGA-W5-AA34-01A-11D-A417-09 TCGA-W5-AA34-10A-01D-A41A-09 g.chr4:164050124T>G c.1410A>C c.(1408-1410)ccA>ccC p.P470P COAD 4 164050137 164050137 + Missense_Mutation SNP T T C TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr4:164050137T>C c.1397A>G c.(1396-1398)tAc>tGc p.Y466C COAD 4 164050212 164050212 + Frame_Shift_Del DEL G G - TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr4:164050212delG c.1322delC c.(1321-1323)ccafs p.P446fs COAD 4 164067003 164067003 + Silent SNP A A G TCGA-CM-6679-01A-11D-1835-10 TCGA-CM-6679-10A-01D-1835-10 g.chr4:164067003A>G c.648T>C c.(646-648)tcT>tcC p.S216S COAD 4 164067005 164067005 + Missense_Mutation SNP A A G TCGA-DM-A28H-01A-11D-A16V-10 TCGA-DM-A28H-10A-01D-A16V-10 g.chr4:164067005A>G c.646T>C c.(646-648)Tct>Cct p.S216P COADREAD 4 164050137 164050137 + Missense_Mutation SNP T T C TCGA-AZ-6598-01A-11D-1771-10 TCGA-AZ-6598-11A-01D-1771-10 g.chr4:164050137T>C c.1397A>G c.(1396-1398)tAc>tGc p.Y466C COADREAD 4 164050212 164050212 + Frame_Shift_Del DEL G G - TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr4:164050212delG c.1322delC c.(1321-1323)ccafs p.P446fs COADREAD 4 164061373 164061373 + Splice_Site SNP A A C TCGA-G5-6235-01A-11D-1733-10 TCGA-G5-6235-10A-01D-1733-10 g.chr4:164061373A>C c.e5+1 COADREAD 4 164067003 164067003 + Silent SNP A A G TCGA-CM-6679-01A-11D-1835-10 TCGA-CM-6679-10A-01D-1835-10 g.chr4:164067003A>G c.648T>C c.(646-648)tcT>tcC p.S216S COADREAD 4 164067005 164067005 + Missense_Mutation SNP A A G TCGA-DM-A28H-01A-11D-A16V-10 TCGA-DM-A28H-10A-01D-A16V-10 g.chr4:164067005A>G c.646T>C c.(646-648)Tct>Cct p.S216P COADREAD 4 164069568 164069568 + Nonsense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr4:164069568C>A c.559G>T c.(559-561)Gaa>Taa p.E187* DLBC 4 164087753 164087753 + Missense_Mutation SNP G G A TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr4:164087753G>A c.127C>T c.(127-129)Ccg>Tcg p.P43S ESCA 4 164050200 164050200 + Frame_Shift_Del DEL G G - TCGA-JY-A6FH-01A-11D-A33E-09 TCGA-JY-A6FH-10A-01D-A33H-09 g.chr4:164050200delG c.1334delC c.(1333-1335)ccafs p.P446fs ESCA 4 164061390 164061390 + Missense_Mutation SNP G G T TCGA-VR-AA7I-01A-11D-A403-09 TCGA-VR-AA7I-10A-01D-A403-09 g.chr4:164061390G>T c.863C>A c.(862-864)aCa>aAa p.T288K GBM 4 164050096 164050096 + Missense_Mutation SNP G G C TCGA-16-1048-01B-01D-1353-08 TCGA-16-1048-10A-01D-1353-08 g.chr4:164050096G>C c.1438C>G c.(1438-1440)Cca>Gca p.P480A GBM 4 164050120 164050120 + Missense_Mutation SNP G G A TCGA-76-4934-01A-01D-1486-08 TCGA-76-4934-10A-01D-1486-08 g.chr4:164050120G>A c.1414C>T c.(1414-1416)Cct>Tct p.P472S GBM 4 164054388 164054388 + Silent SNP A A G TCGA-32-2638-01A-01D-1495-08 TCGA-32-2638-10A-01D-1495-08 g.chr4:164054388A>G c.951T>C c.(949-951)gaT>gaC p.D317D GBMLGG 4 164050096 164050096 + Missense_Mutation SNP G G C TCGA-16-1048-01B-01D-1353-08 TCGA-16-1048-10A-01D-1353-08 g.chr4:164050096G>C c.1438C>G c.(1438-1440)Cca>Gca p.P480A GBMLGG 4 164050120 164050120 + Missense_Mutation SNP G G A TCGA-76-4934-01A-01D-1486-08 TCGA-76-4934-10A-01D-1486-08 g.chr4:164050120G>A c.1414C>T c.(1414-1416)Cct>Tct p.P472S GBMLGG 4 164050323 164050323 + Missense_Mutation SNP T T C TCGA-IK-8125-01A-11D-2253-08 TCGA-IK-8125-10A-01D-2253-08 g.chr4:164050323T>C c.1211A>G c.(1210-1212)cAg>cGg p.Q404R GBMLGG 4 164050411 164050411 + Nonsense_Mutation SNP G G A TCGA-DU-A7TB-01A-11D-A33T-08 TCGA-DU-A7TB-10A-01D-A33W-08 g.chr4:164050411G>A c.1123C>T c.(1123-1125)Cga>Tga p.R375* GBMLGG 4 164050495 164050495 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr4:164050495C>A c.1039G>T c.(1039-1041)Gat>Tat p.D347Y GBMLGG 4 164054388 164054388 + Silent SNP A A G TCGA-32-2638-01A-01D-1495-08 TCGA-32-2638-10A-01D-1495-08 g.chr4:164054388A>G c.951T>C c.(949-951)gaT>gaC p.D317D HNSC 4 164050069 164050069 + Missense_Mutation SNP G G A TCGA-CR-6472-01A-11D-1870-08 TCGA-CR-6472-10A-01D-1870-08 g.chr4:164050069G>A c.1465C>T c.(1465-1467)Cat>Tat p.H489Y HNSC 4 164050333 164050333 + Missense_Mutation SNP T T C TCGA-DQ-7588-01A-11D-2078-08 TCGA-DQ-7588-10B-01D-2078-08 g.chr4:164050333T>C c.1201A>G c.(1201-1203)Atg>Gtg p.M401V HNSC 4 164061530 164061530 + Silent SNP G G A TCGA-BA-A6DF-01A-11D-A30E-08 TCGA-BA-A6DF-10A-01D-A30H-08 g.chr4:164061530G>A c.723C>T c.(721-723)ttC>ttT p.F241F HNSC 4 164069513 164069513 + Nonsense_Mutation SNP G G C TCGA-CN-6011-01A-11D-1683-08 TCGA-CN-6011-10A-01D-1683-08 g.chr4:164069513G>C c.614C>G c.(613-615)tCa>tGa p.S205* HNSC 4 164087774 164087774 + Missense_Mutation SNP G G A TCGA-CR-7364-01A-11D-2012-08 TCGA-CR-7364-10A-01D-2013-08 g.chr4:164087774G>A c.106C>T c.(106-108)Cct>Tct p.P36S HNSC 4 164087806 164087806 + Missense_Mutation SNP T T C TCGA-CN-A6V6-01A-12D-A34J-08 TCGA-CN-A6V6-10A-01D-A34M-08 g.chr4:164087806T>C c.74A>G c.(73-75)gAa>gGa p.E25G KIPAN 4 164050071 164050071 + Missense_Mutation SNP G G T TCGA-BP-5185-01A-01D-1429-08 TCGA-BP-5185-11A-01D-1429-08 g.chr4:164050071G>T c.1463C>A c.(1462-1464)tCt>tAt p.S488Y KIPAN 4 164050121 164050121 + Silent SNP G G A TCGA-BQ-5882-01A-11D-1589-08 TCGA-BQ-5882-11A-01D-1589-08 g.chr4:164050121G>A c.1413C>T c.(1411-1413)ccC>ccT p.P471P KIPAN 4 164050358 164050358 + Silent SNP A A G TCGA-B8-5158-01A-01D-1421-08 TCGA-B8-5158-10A-01D-1421-08 g.chr4:164050358A>G c.1176T>C c.(1174-1176)ccT>ccC p.P392P KIPAN 4 164087855 164087855 + Missense_Mutation SNP C C A TCGA-BP-5182-01A-01D-1429-08 TCGA-BP-5182-11A-01D-1429-08 g.chr4:164087855C>A c.25G>T c.(25-27)Gct>Tct p.A9S KIRC 4 164050071 164050071 + Missense_Mutation SNP G G T TCGA-BP-5185-01A-01D-1429-08 TCGA-BP-5185-11A-01D-1429-08 g.chr4:164050071G>T c.1463C>A c.(1462-1464)tCt>tAt p.S488Y KIRC 4 164050358 164050358 + Silent SNP A A G TCGA-B8-5158-01A-01D-1421-08 TCGA-B8-5158-10A-01D-1421-08 g.chr4:164050358A>G c.1176T>C c.(1174-1176)ccT>ccC p.P392P KIRC 4 164087855 164087855 + Missense_Mutation SNP C C A TCGA-BP-5182-01A-01D-1429-08 TCGA-BP-5182-11A-01D-1429-08 g.chr4:164087855C>A c.25G>T c.(25-27)Gct>Tct p.A9S KIRP 4 164050121 164050121 + Silent SNP G G A TCGA-BQ-5882-01A-11D-1589-08 TCGA-BQ-5882-11A-01D-1589-08 g.chr4:164050121G>A c.1413C>T c.(1411-1413)ccC>ccT p.P471P LGG 4 164050323 164050323 + Missense_Mutation SNP T T C TCGA-IK-8125-01A-11D-2253-08 TCGA-IK-8125-10A-01D-2253-08 g.chr4:164050323T>C c.1211A>G c.(1210-1212)cAg>cGg p.Q404R LGG 4 164050411 164050411 + Nonsense_Mutation SNP G G A TCGA-DU-A7TB-01A-11D-A33T-08 TCGA-DU-A7TB-10A-01D-A33W-08 g.chr4:164050411G>A c.1123C>T c.(1123-1125)Cga>Tga p.R375* LGG 4 164050495 164050495 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr4:164050495C>A c.1039G>T c.(1039-1041)Gat>Tat p.D347Y LIHC 4 164058390 164058390 + Silent SNP T T C TCGA-CC-A3MA-01A-11D-A20W-10 TCGA-CC-A3MA-10A-01D-A20W-10 g.chr4:164058390T>C c.891A>G c.(889-891)tcA>tcG p.S297S LIHC 4 164061471 164061471 + Missense_Mutation SNP T T C TCGA-DD-A3A9-01A-11D-A25V-10 TCGA-DD-A3A9-11A-11D-A25V-10 g.chr4:164061471T>C c.782A>G c.(781-783)cAc>cGc p.H261R LIHC 4 164085383 164085383 + Missense_Mutation SNP C C G TCGA-DD-A3A0-01A-11D-A20W-10 TCGA-DD-A3A0-11A-11D-A20W-10 g.chr4:164085383C>G c.526G>C c.(526-528)Gaa>Caa p.E176Q LUAD 4 164050298 164050298 + Silent SNP C C T TCGA-97-A4M5-01A-11D-A24P-08 TCGA-97-A4M5-10A-01D-A24P-08 g.chr4:164050298C>T c.1236G>A c.(1234-1236)caG>caA p.Q412Q LUAD 4 164050300 164050300 + Nonsense_Mutation SNP G G A TCGA-78-7150-01A-21D-2036-08 TCGA-78-7150-10A-01D-2036-08 g.chr4:164050300G>A c.1234C>T c.(1234-1236)Cag>Tag p.Q412* LUAD 4 164061434 164061434 + Missense_Mutation SNP C C T TCGA-97-7546-01A-11D-2036-08 TCGA-97-7546-10A-01D-2036-08 g.chr4:164061434C>T c.819G>A c.(817-819)atG>atA p.M273I LUAD 4 164061457 164061457 + Missense_Mutation SNP C C T TCGA-75-5126-01A-01D-1753-08 TCGA-75-5126-10A-01D-1753-08 g.chr4:164061457C>T c.796G>A c.(796-798)Ggt>Agt p.G266S LUAD 4 164085484 164085484 + Missense_Mutation SNP G G C TCGA-35-4122-01A-01D-1105-08 TCGA-35-4122-10A-01D-1105-08 g.chr4:164085484G>C c.425C>G c.(424-426)tCt>tGt p.S142C LUAD 4 164087652 164087652 + Silent SNP G G A TCGA-55-A490-01A-11D-A24D-08 TCGA-55-A490-10A-01D-A24F-08 g.chr4:164087652G>A c.228C>T c.(226-228)gcC>gcT p.A76A LUAD 4 164087830 164087830 + Missense_Mutation SNP T T A TCGA-44-7671-01A-11D-2063-08 TCGA-44-7671-10A-01D-2063-08 g.chr4:164087830T>A c.50A>T c.(49-51)aAt>aTt p.N17I LUAD 4 164087832 164087832 + Silent SNP G G A TCGA-44-6144-01A-11D-1753-08 TCGA-44-6144-10A-01D-1753-08 g.chr4:164087832G>A c.48C>T c.(46-48)ttC>ttT p.F16F LUSC 4 164050062 164050062 + Missense_Mutation SNP C C T TCGA-66-2759-01A-01D-1522-08 TCGA-66-2759-11A-01D-1522-08 g.chr4:164050062C>T c.1472G>A c.(1471-1473)gGa>gAa p.G491E LUSC 4 164050110 164050110 + Missense_Mutation SNP G G A TCGA-37-4135-01A-01D-1352-08 TCGA-37-4135-10A-01D-1352-08 g.chr4:164050110G>A c.1424C>T c.(1423-1425)cCa>cTa p.P475L LUSC 4 164050300 164050300 + Nonsense_Mutation SNP G G A TCGA-39-5031-01A-01D-1441-08 TCGA-39-5031-11A-01D-1441-08 g.chr4:164050300G>A c.1234C>T c.(1234-1236)Cag>Tag p.Q412* LUSC 4 164050477 164050477 + Missense_Mutation SNP G G C TCGA-66-2782-01A-01D-1522-08 TCGA-66-2782-11A-01D-1522-08 g.chr4:164050477G>C c.1057C>G c.(1057-1059)Cag>Gag p.Q353E LUSC 4 164054361 164054361 + Silent SNP C C T TCGA-66-2783-01A-01D-1267-08 TCGA-66-2783-11A-01D-1267-08 g.chr4:164054361C>T c.978G>A c.(976-978)agG>agA p.R326R LUSC 4 164087748 164087748 + Silent SNP T T C TCGA-22-5472-01A-01D-1632-08 TCGA-22-5472-11A-11D-1632-08 g.chr4:164087748T>C c.132A>G c.(130-132)ctA>ctG p.L44L OV 4 164050415 164050415 + Missense_Mutation SNP G G C TCGA-10-0930-01A-02W-0421-09 TCGA-10-0930-11A-01W-0977-09 g.chr4:164050415G>C c.1119C>G c.(1117-1119)ttC>ttG p.F373L OV 4 164061530 164061530 + Silent SNP G G A TCGA-36-2551-01A-01D-1526-09 TCGA-36-2551-10A-01D-1526-09 g.chr4:164061530G>A c.723C>T c.(721-723)ttC>ttT p.F241F OV 4 164067004 164067004 + Missense_Mutation SNP G G C TCGA-09-2056-01B-01W-0722-08 TCGA-09-2056-11A-01W-0722-08 g.chr4:164067004G>C c.647C>G c.(646-648)tCt>tGt p.S216C PAAD 4 164050124 164050124 + Silent SNP T T G TCGA-2L-AAQJ-01A-12D-A397-08 TCGA-2L-AAQJ-11A-11D-A39A-08 g.chr4:164050124T>G c.1410A>C c.(1408-1410)ccA>ccC p.P470P PAAD 4 164050124 164050124 + Silent SNP T T G TCGA-3A-A9IJ-01A-11D-A397-08 TCGA-3A-A9IJ-10A-01D-A39A-08 g.chr4:164050124T>G c.1410A>C c.(1408-1410)ccA>ccC p.P470P PAAD 4 164050124 164050124 + Silent SNP T T G TCGA-3A-A9IU-01A-11D-A397-08 TCGA-3A-A9IU-10A-01D-A39A-08 g.chr4:164050124T>G c.1410A>C c.(1408-1410)ccA>ccC p.P470P PAAD 4 164050124 164050124 + Silent SNP T T G TCGA-XD-AAUL-01A-21D-A397-08 TCGA-XD-AAUL-10A-01D-A39A-08 g.chr4:164050124T>G c.1410A>C c.(1408-1410)ccA>ccC p.P470P PAAD 4 164050411 164050411 + Nonsense_Mutation SNP G G A TCGA-IB-A5SO-01A-11D-A32N-08 TCGA-IB-A5SO-10A-01D-A32N-08 g.chr4:164050411G>A c.1123C>T c.(1123-1125)Cga>Tga p.R375* PCPG 4 164050124 164050124 + Silent SNP T T C TCGA-QR-A70U-01A-11D-A35D-08 TCGA-QR-A70U-10A-01D-A35B-08 g.chr4:164050124T>C c.1410A>G c.(1408-1410)ccA>ccG p.P470P PRAD 4 164050124 164050124 + Silent SNP T T G TCGA-EJ-5531-01A-01D-1576-08 TCGA-EJ-5531-10A-01D-1577-08 g.chr4:164050124T>G c.1410A>C c.(1408-1410)ccA>ccC p.P470P PRAD 4 164050124 164050124 + Silent SNP T T G TCGA-G9-6373-01A-11D-1786-08 TCGA-G9-6373-10A-01D-1786-08 g.chr4:164050124T>G c.1410A>C c.(1408-1410)ccA>ccC p.P470P PRAD 4 164061475 164061475 + Missense_Mutation SNP C C A TCGA-XK-AAJ3-01A-11D-A41K-08 TCGA-XK-AAJ3-10A-01D-A41N-08 g.chr4:164061475C>A c.778G>T c.(778-780)Gat>Tat p.D260Y READ 4 164061373 164061373 + Splice_Site SNP A A C TCGA-G5-6235-01A-11D-1733-10 TCGA-G5-6235-10A-01D-1733-10 g.chr4:164061373A>C c.e5+1 READ 4 164069568 164069568 + Nonsense_Mutation SNP C C A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr4:164069568C>A c.559G>T c.(559-561)Gaa>Taa p.E187* SKCM 4 164050071 164050071 + Missense_Mutation SNP G G A TCGA-EE-A3AF-06A-11D-A196-08 TCGA-EE-A3AF-10A-01D-A198-08 g.chr4:164050071G>A c.1463C>T c.(1462-1464)tCt>tTt p.S488F SKCM 4 164050305 164050305 + Missense_Mutation SNP G G T TCGA-D3-A51G-06A-11D-A25O-08 TCGA-D3-A51G-10A-01D-A25O-08 g.chr4:164050305G>T c.1229C>A c.(1228-1230)cCt>cAt p.P410H SKCM 4 164050306 164050306 + Missense_Mutation SNP G G A TCGA-OD-A75X-06A-12D-A32N-08 TCGA-OD-A75X-10A-01D-A32N-08 g.chr4:164050306G>A c.1228C>T c.(1228-1230)Cct>Tct p.P410S SKCM 4 164050415 164050415 + Silent SNP G G A TCGA-D9-A1JW-06A-11D-A19A-08 TCGA-D9-A1JW-10A-01D-A19A-08 g.chr4:164050415G>A c.1119C>T c.(1117-1119)ttC>ttT p.F373F SKCM 4 164066932 164066932 + Splice_Site SNP A A G TCGA-DA-A1I5-06A-11D-A197-08 TCGA-DA-A1I5-10A-01D-A199-08 g.chr4:164066932A>G c.e4+1 SKCM 4 164087677 164087677 + Missense_Mutation SNP T T G TCGA-DA-A1IA-06A-11D-A196-08 TCGA-DA-A1IA-10A-01D-A198-08 g.chr4:164087677T>G c.203A>C c.(202-204)cAg>cCg p.Q68P BLCA 5 150411896 150411896 + Missense_Mutation SNP G G T TCGA-XF-AAN5-01A-11D-A42E-08 TCGA-XF-AAN5-10A-01D-A42H-08 g.chr5:150411896G>T c.1828C>A c.(1828-1830)Cag>Aag p.Q610K BLCA 5 150422117 150422117 + Missense_Mutation SNP T T G TCGA-FD-A62O-01A-11D-A30E-08 TCGA-FD-A62O-10A-01D-A30H-08 g.chr5:150422117T>G c.1118A>C c.(1117-1119)aAg>aCg p.K373T BLCA 5 150422486 150422486 + Missense_Mutation SNP G G A TCGA-CF-A3MI-01A-11D-A20D-08 TCGA-CF-A3MI-10A-01D-A20D-08 g.chr5:150422486G>A c.973C>T c.(973-975)Cgg>Tgg p.R325W BLCA 5 150441747 150441747 + Missense_Mutation SNP G G C TCGA-XF-AAN5-01A-11D-A42E-08 TCGA-XF-AAN5-10A-01D-A42H-08 g.chr5:150441747G>C c.298C>G c.(298-300)Ccc>Gcc p.P100A BLCA 5 150444592 150444592 + Missense_Mutation SNP G G A TCGA-XF-AAMX-01A-11D-A42E-08 TCGA-XF-AAMX-10A-01D-A42H-08 g.chr5:150444592G>A c.65C>T c.(64-66)tCc>tTc p.S22F BRCA 5 150425443 150425443 + Missense_Mutation SNP C C T TCGA-BH-A0HF-01A-11W-A071-09 TCGA-BH-A0HF-10A-01W-A071-09 g.chr5:150425443C>T c.915G>A c.(913-915)atG>atA p.M305I BRCA 5 150425460 150425460 + Missense_Mutation SNP C C T TCGA-D8-A27V-01A-12D-A17D-09 TCGA-D8-A27V-10A-01D-A17D-09 g.chr5:150425460C>T c.898G>A c.(898-900)Gag>Aag p.E300K BRCA 5 150439923 150439923 + Missense_Mutation SNP C C T TCGA-BH-A0HP-01A-12D-A099-09 TCGA-BH-A0HP-10A-01D-A099-09 g.chr5:150439923C>T c.391G>A c.(391-393)Gag>Aag p.E131K COAD 5 150410296 150410296 + Frame_Shift_Del DEL T T - TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr5:150410296delT c.1889delA c.(1888-1890)aatfs p.N630fs COAD 5 150410296 150410296 + Frame_Shift_Del DEL T T - TCGA-CK-5916-01A-11D-1650-10 TCGA-CK-5916-10A-01D-1650-10 g.chr5:150410296delT c.1889delA c.(1888-1890)aatfs p.N630fs COAD 5 150411907 150411907 + Missense_Mutation SNP C C T TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr5:150411907C>T c.1817G>A c.(1816-1818)cGa>cAa p.R606Q COAD 5 150413182 150413182 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr5:150413182C>T c.1766G>A c.(1765-1767)cGc>cAc p.R589H COAD 5 150413340 150413340 + Silent SNP A A G TCGA-CM-6674-01A-11D-1835-10 TCGA-CM-6674-10A-01D-1835-10 g.chr5:150413340A>G c.1608T>C c.(1606-1608)caT>caC p.H536H COAD 5 150415226 150415226 + Missense_Mutation SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr5:150415226G>A c.1438C>T c.(1438-1440)Cgt>Tgt p.R480C COAD 5 150436467 150436467 + Missense_Mutation SNP G G A TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr5:150436467G>A c.487C>T c.(487-489)Cgc>Tgc p.R163C COAD 5 150439898 150439898 + Missense_Mutation SNP C C T TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr5:150439898C>T c.416G>A c.(415-417)aGc>aAc p.S139N COADREAD 5 150410296 150410296 + Frame_Shift_Del DEL T T - TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr5:150410296delT c.1889delA c.(1888-1890)aatfs p.N630fs COADREAD 5 150410296 150410296 + Frame_Shift_Del DEL T T - TCGA-CK-5916-01A-11D-1650-10 TCGA-CK-5916-10A-01D-1650-10 g.chr5:150410296delT c.1889delA c.(1888-1890)aatfs p.N630fs COADREAD 5 150411907 150411907 + Missense_Mutation SNP C C T TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr5:150411907C>T c.1817G>A c.(1816-1818)cGa>cAa p.R606Q COADREAD 5 150413182 150413182 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr5:150413182C>T c.1766G>A c.(1765-1767)cGc>cAc p.R589H COADREAD 5 150413340 150413340 + Silent SNP A A G TCGA-CM-6674-01A-11D-1835-10 TCGA-CM-6674-10A-01D-1835-10 g.chr5:150413340A>G c.1608T>C c.(1606-1608)caT>caC p.H536H COADREAD 5 150415226 150415226 + Missense_Mutation SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr5:150415226G>A c.1438C>T c.(1438-1440)Cgt>Tgt p.R480C COADREAD 5 150436467 150436467 + Missense_Mutation SNP G G A TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr5:150436467G>A c.487C>T c.(487-489)Cgc>Tgc p.R163C COADREAD 5 150439898 150439898 + Missense_Mutation SNP C C T TCGA-AA-3710-01A-01W-0995-10 TCGA-AA-3710-10A-01W-0995-10 g.chr5:150439898C>T c.416G>A c.(415-417)aGc>aAc p.S139N DLBC 5 150441711 150441711 + Missense_Mutation SNP G G C TCGA-G8-6907-01A-11D-2210-10 TCGA-G8-6907-14A-01D-2210-10 g.chr5:150441711G>C c.334C>G c.(334-336)Cca>Gca p.P112A ESCA 5 150410284 150410284 + Missense_Mutation SNP C C G TCGA-IG-A50L-01A-11D-A27G-09 TCGA-IG-A50L-10A-01D-A27G-09 g.chr5:150410284C>G c.1901G>C c.(1900-1902)gGg>gCg p.G634A ESCA 5 150410286 150410286 + Missense_Mutation SNP C C A TCGA-R6-A6Y0-01B-11D-A33E-09 TCGA-R6-A6Y0-10A-01D-A33H-09 g.chr5:150410286C>A c.1899G>T c.(1897-1899)gaG>gaT p.E633D ESCA 5 150410288 150410288 + Missense_Mutation SNP C C G TCGA-VR-AA7B-01A-31D-A403-09 TCGA-VR-AA7B-10A-01D-A403-09 g.chr5:150410288C>G c.1897G>C c.(1897-1899)Gag>Cag p.E633Q ESCA 5 150411870 150411870 + Silent SNP G G A TCGA-IC-A6RF-01A-13D-A33E-09 TCGA-IC-A6RF-10A-21D-A33H-09 g.chr5:150411870G>A c.1854C>T c.(1852-1854)ccC>ccT p.P618P ESCA 5 150443229 150443229 + Silent SNP C C A TCGA-LN-A5U5-01A-21D-A28B-09 TCGA-LN-A5U5-10A-01D-A28E-09 g.chr5:150443229C>A c.216G>T c.(214-216)ctG>ctT p.L72L GBMLGG 5 150425452 150425454 + In_Frame_Del DEL CTT CTT - TCGA-HW-7490-01A-11D-2024-08 TCGA-HW-7490-10A-01D-2024-08 g.chr5:150425452_150425454delCTT c.904_906delAAG c.(904-906)aagdel p.K302del GBMLGG 5 150444602 150444602 + Nonsense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr5:150444602C>A c.55G>T c.(55-57)Gga>Tga p.G19* HNSC 5 150410275 150410275 + Nonstop_Mutation SNP C C G TCGA-CV-A6K2-01A-11D-A31L-08 TCGA-CV-A6K2-10A-01D-A31J-08 g.chr5:150410275C>G c.1910G>C c.(1909-1911)tGa>tCa p.*637S HNSC 5 150415257 150415257 + Silent SNP G G A TCGA-CN-4723-01A-01D-1434-08 TCGA-CN-4723-10A-01D-1434-08 g.chr5:150415257G>A c.1407C>T c.(1405-1407)ttC>ttT p.F469F HNSC 5 150422172 150422172 + Missense_Mutation SNP C C T TCGA-RS-A6TO-01A-32D-A34J-08 TCGA-RS-A6TO-10A-01D-A34M-08 g.chr5:150422172C>T c.1063G>A c.(1063-1065)Gag>Aag p.E355K HNSC 5 150422486 150422486 + Missense_Mutation SNP G G A TCGA-F7-8489-01A-31D-2394-08 TCGA-F7-8489-10A-01D-2394-08 g.chr5:150422486G>A c.973C>T c.(973-975)Cgg>Tgg p.R325W HNSC 5 150436431 150436431 + Missense_Mutation SNP G G A TCGA-CV-A6JD-01A-11D-A31L-08 TCGA-CV-A6JD-10A-01D-A31J-08 g.chr5:150436431G>A c.523C>T c.(523-525)Ccg>Tcg p.P175S HNSC 5 150436497 150436497 + Missense_Mutation SNP C C T TCGA-T3-A92N-01A-11D-A391-08 TCGA-T3-A92N-10A-01D-A394-08 g.chr5:150436497C>T c.457G>A c.(457-459)Gag>Aag p.E153K HNSC 5 150444653 150444653 + Missense_Mutation SNP C C T TCGA-UF-A71D-01A-12D-A34J-08 TCGA-UF-A71D-10B-01D-A34M-08 g.chr5:150444653C>T c.4G>A c.(4-6)Gaa>Aaa p.E2K KIPAN 5 150422134 150422134 + Silent SNP G G C TCGA-AK-3428-01A-02D-1361-10 TCGA-AK-3428-10A-01D-1361-10 g.chr5:150422134G>C c.1101C>G c.(1099-1101)ctC>ctG p.L367L KIPAN 5 150443282 150443283 + In_Frame_Ins INS - - ATA TCGA-GL-A9DC-01A-11D-A36X-10 TCGA-GL-A9DC-10A-01D-A370-10 g.chr5:150443282_150443283insATA c.162_163insTAT c.(160-165)atggaa>atgTATgaa p.54_55ME>MYE KIPAN 5 150443283 150443286 + Frame_Shift_Del DEL CATC CATC - TCGA-GL-A9DC-01A-11D-A36X-10 TCGA-GL-A9DC-10A-01D-A370-10 g.chr5:150443283_150443286delCATC c.159_162delGATG c.(157-162)cagatgfs p.QM53fs KIPAN 5 150443286 150443286 + Silent SNP C C T TCGA-GL-A9DC-01A-11D-A36X-10 TCGA-GL-A9DC-10A-01D-A370-10 g.chr5:150443286C>T c.159G>A c.(157-159)caG>caA p.Q53Q KIPAN 5 150444534 150444534 + Silent SNP C C G TCGA-A4-8517-01A-11D-2396-08 TCGA-A4-8517-10A-01D-2396-08 g.chr5:150444534C>G c.123G>C c.(121-123)ggG>ggC p.G41G KIRC 5 150422134 150422134 + Silent SNP G G C TCGA-AK-3428-01A-02D-1361-10 TCGA-AK-3428-10A-01D-1361-10 g.chr5:150422134G>C c.1101C>G c.(1099-1101)ctC>ctG p.L367L KIRP 5 150443282 150443283 + In_Frame_Ins INS - - ATA TCGA-GL-A9DC-01A-11D-A36X-10 TCGA-GL-A9DC-10A-01D-A370-10 g.chr5:150443282_150443283insATA c.162_163insTAT c.(160-165)atggaa>atgTATgaa p.54_55ME>MYE KIRP 5 150443283 150443286 + Frame_Shift_Del DEL CATC CATC - TCGA-GL-A9DC-01A-11D-A36X-10 TCGA-GL-A9DC-10A-01D-A370-10 g.chr5:150443283_150443286delCATC c.159_162delGATG c.(157-162)cagatgfs p.QM53fs KIRP 5 150443286 150443286 + Silent SNP C C T TCGA-GL-A9DC-01A-11D-A36X-10 TCGA-GL-A9DC-10A-01D-A370-10 g.chr5:150443286C>T c.159G>A c.(157-159)caG>caA p.Q53Q KIRP 5 150444534 150444534 + Silent SNP C C G TCGA-A4-8517-01A-11D-2396-08 TCGA-A4-8517-10A-01D-2396-08 g.chr5:150444534C>G c.123G>C c.(121-123)ggG>ggC p.G41G LGG 5 150425452 150425454 + In_Frame_Del DEL CTT CTT - TCGA-HW-7490-01A-11D-2024-08 TCGA-HW-7490-10A-01D-2024-08 g.chr5:150425452_150425454delCTT c.904_906delAAG c.(904-906)aagdel p.K302del LGG 5 150444602 150444602 + Nonsense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr5:150444602C>A c.55G>T c.(55-57)Gga>Tga p.G19* LIHC 5 150410290 150410290 + Frame_Shift_Del DEL C C - TCGA-4R-AA8I-01A-11D-A382-10 TCGA-4R-AA8I-10B-01D-A385-10 g.chr5:150410290delC c.1895delG c.(1894-1896)cgtfs p.R632fs LIHC 5 150415262 150415262 + Missense_Mutation SNP T T C TCGA-DD-AAVS-01A-11D-A40R-10 TCGA-DD-AAVS-10A-01D-A40U-10 g.chr5:150415262T>C c.1402A>G c.(1402-1404)Atc>Gtc p.I468V LIHC 5 150436496 150436496 + Missense_Mutation SNP T T C TCGA-BC-A10W-01A-11D-A12Z-10 TCGA-BC-A10W-11A-11D-A12Z-10 g.chr5:150436496T>C c.458A>G c.(457-459)gAg>gGg p.E153G LUAD 5 150422188 150422188 + Silent SNP C C T TCGA-55-8085-01A-11D-2238-08 TCGA-55-8085-10A-01D-2238-08 g.chr5:150422188C>T c.1047G>A c.(1045-1047)gtG>gtA p.V349V LUAD 5 150422465 150422465 + Missense_Mutation SNP C C T TCGA-78-7158-01A-11D-2036-08 TCGA-78-7158-10A-01D-2036-08 g.chr5:150422465C>T c.994G>A c.(994-996)Gag>Aag p.E332K LUAD 5 150439923 150439923 + Missense_Mutation SNP C C T TCGA-17-Z044-01A-01W-0746-08 TCGA-17-Z044-11A-01W-0746-08 g.chr5:150439923C>T c.391G>A c.(391-393)Gag>Aag p.E131K LUAD 5 150444522 150444522 + Splice_Site SNP T T C TCGA-55-8089-01A-11D-2238-08 TCGA-55-8089-10A-01D-2238-08 g.chr5:150444522T>C c.135A>G c.(133-135)ttA>ttG p.L45L LUSC 5 150416412 150416412 + Missense_Mutation SNP C C A TCGA-60-2698-01A-01D-1522-08 TCGA-60-2698-11A-01D-1522-08 g.chr5:150416412C>A c.1334G>T c.(1333-1335)gGa>gTa p.G445V LUSC 5 150436437 150436437 + Missense_Mutation SNP C C T TCGA-66-2785-01A-01D-1522-08 TCGA-66-2785-11A-01D-1522-08 g.chr5:150436437C>T c.517G>A c.(517-519)Gag>Aag p.E173K OV 5 150441739 150441739 + Silent SNP G G C TCGA-04-1356-01A-01W-0492-08 TCGA-04-1356-11A-01W-0492-08 g.chr5:150441739G>C c.306C>G c.(304-306)gcC>gcG p.A102A PRAD 5 150415234 150415234 + Missense_Mutation SNP C C T TCGA-QU-A6IO-01A-11D-A31L-08 TCGA-QU-A6IO-10A-01D-A31J-08 g.chr5:150415234C>T c.1430G>A c.(1429-1431)cGc>cAc p.R477H PRAD 5 150422163 150422163 + Nonsense_Mutation SNP G G A TCGA-HC-A6AP-01A-11D-A30E-08 TCGA-HC-A6AP-10A-01D-A30H-08 g.chr5:150422163G>A c.1072C>T c.(1072-1074)Cag>Tag p.Q358* PRAD 5 150436423 150436423 + Silent SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr5:150436423G>A c.531C>T c.(529-531)caC>caT p.H177H PRAD 5 150439883 150439883 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr5:150439883G>A c.431C>T c.(430-432)gCg>gTg p.A144V PRAD 5 150444612 150444612 + Silent SNP G G A TCGA-EJ-A65J-01A-11D-A30X-08 TCGA-EJ-A65J-10A-01D-A30X-08 g.chr5:150444612G>A c.45C>T c.(43-45)agC>agT p.S15S SARC 5 150413231 150413231 + Missense_Mutation SNP G G A TCGA-QC-A7B5-01A-11D-A33E-09 TCGA-QC-A7B5-11A-11D-A33H-09 g.chr5:150413231G>A c.1717C>T c.(1717-1719)Ccc>Tcc p.P573S SKCM 5 150411874 150411874 + Missense_Mutation SNP G G A TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr5:150411874G>A c.1850C>T c.(1849-1851)cCt>cTt p.P617L SKCM 5 150411892 150411892 + Missense_Mutation SNP C C T TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr5:150411892C>T c.1832G>A c.(1831-1833)aGc>aAc p.S611N SKCM 5 150411944 150411944 + Splice_Site SNP G G A TCGA-EE-A2MP-06A-11D-A197-08 TCGA-EE-A2MP-10A-01D-A199-08 g.chr5:150411944G>A c.1780C>T c.(1780-1782)Ccg>Tcg p.P594S SKCM 5 150413312 150413312 + Missense_Mutation SNP C C G TCGA-EE-A3AC-06A-11D-A196-08 TCGA-EE-A3AC-10A-01D-A198-08 g.chr5:150413312C>G c.1636G>C c.(1636-1638)Ggg>Cgg p.G546R SKCM 5 150416401 150416401 + Missense_Mutation SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr5:150416401G>A c.1345C>T c.(1345-1347)Ctc>Ttc p.L449F SKCM 5 150416402 150416402 + Silent SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr5:150416402G>A c.1344C>T c.(1342-1344)gcC>gcT p.A448A SKCM 5 150436378 150436378 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr5:150436378G>A c.576C>T c.(574-576)aaC>aaT p.N192N SKCM 5 150436501 150436501 + Silent SNP G G A TCGA-EE-A2ML-06A-11D-A197-08 TCGA-EE-A2ML-10A-01D-A199-08 g.chr5:150436501G>A c.453C>T c.(451-453)ccC>ccT p.P151P SKCM 5 150439957 150439957 + Splice_Site SNP C C A TCGA-EE-A184-06A-11D-A196-08 TCGA-EE-A184-10B-01D-A198-08 g.chr5:150439957C>A c.e5-1 SKCM 5 150443209 150443209 + Missense_Mutation SNP G G A TCGA-FR-A3YN-06A-11D-A23B-08 TCGA-FR-A3YN-10A-01D-A23B-08 g.chr5:150443209G>A c.236C>T c.(235-237)tCc>tTc p.S79F

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-US 5 150407000 150407000 single base substitution C T downstream_gene_variant BLCA-US 5 150407039 150407039 single base substitution G C downstream_gene_variant BRCA-EU 5 150404767 150404767 single base substitution C G downstream_gene_variant BRCA-EU 5 150404898 150404898 single base substitution C G downstream_gene_variant BRCA-EU 5 150406962 150406962 single base substitution T G downstream_gene_variant BRCA-EU 5 150411439 150411439 insertion of <=200bp - C downstream_gene_variant BRCA-EU 5 150411439 150411439 insertion of <=200bp - C intron_variant BRCA-EU 5 150419265 150419265 single base substitution G A downstream_gene_variant BRCA-EU 5 150419265 150419265 single base substitution G A intron_variant BRCA-EU 5 150419265 150419265 single base substitution G A upstream_gene_variant BRCA-EU 5 150420828 150420828 single base substitution C A downstream_gene_variant BRCA-EU 5 150420828 150420828 single base substitution C A intron_variant BRCA-EU 5 150420828 150420828 single base substitution C A upstream_gene_variant BRCA-EU 5 150421054 150421054 single base substitution G A downstream_gene_variant BRCA-EU 5 150421054 150421054 single base substitution G A intron_variant BRCA-EU 5 150421054 150421054 single base substitution G A upstream_gene_variant BRCA-EU 5 150422001 150422001 single base substitution C A downstream_gene_variant BRCA-EU 5 150422001 150422001 single base substitution C A intron_variant BRCA-EU 5 150422001 150422001 single base substitution C A upstream_gene_variant BRCA-EU 5 150422300 150422300 single base substitution C T downstream_gene_variant BRCA-EU 5 150422300 150422300 single base substitution C T intron_variant BRCA-EU 5 150422300 150422300 single base substitution C T upstream_gene_variant BRCA-EU 5 150424940 150424940 single base substitution C G downstream_gene_variant BRCA-EU 5 150424940 150424940 single base substitution C G intron_variant BRCA-EU 5 150425347 150425347 single base substitution C T downstream_gene_variant BRCA-EU 5 150425347 150425347 single base substitution C T intron_variant BRCA-EU 5 150429830 150429830 single base substitution C T intron_variant BRCA-EU 5 150429830 150429830 single base substitution C T upstream_gene_variant BRCA-EU 5 150430417 150430417 single base substitution C A intron_variant BRCA-EU 5 150430417 150430417 single base substitution C A upstream_gene_variant BRCA-EU 5 150433023 150433023 single base substitution G C intron_variant BRCA-EU 5 150433023 150433023 single base substitution G C upstream_gene_variant BRCA-EU 5 150433685 150433685 single base substitution G T intron_variant BRCA-EU 5 150433685 150433685 single base substitution G T upstream_gene_variant BRCA-EU 5 150434098 150434098 single base substitution G T intron_variant BRCA-EU 5 150434098 150434098 single base substitution G T upstream_gene_variant BRCA-EU 5 150435194 150435194 single base substitution C A downstream_gene_variant BRCA-EU 5 150435194 150435194 single base substitution C A intron_variant BRCA-EU 5 150435915 150435915 single base substitution A G downstream_gene_variant BRCA-EU 5 150435915 150435915 single base substitution A G intron_variant BRCA-EU 5 150436680 150436680 single base substitution G A downstream_gene_variant BRCA-EU 5 150436680 150436680 single base substitution G A intron_variant BRCA-EU 5 150437227 150437227 single base substitution G A downstream_gene_variant BRCA-EU 5 150437227 150437227 single base substitution G A intron_variant BRCA-EU 5 150438384 150438384 single base substitution C T downstream_gene_variant BRCA-EU 5 150438384 150438384 single base substitution C T intron_variant BRCA-EU 5 150438730 150438730 single base substitution C A downstream_gene_variant BRCA-EU 5 150438730 150438730 single base substitution C A intron_variant BRCA-EU 5 150440457 150440457 single base substitution C T intron_variant BRCA-EU 5 150443891 150443891 single base substitution G A intron_variant BRCA-EU 5 150443891 150443891 single base substitution G A upstream_gene_variant BRCA-EU 5 150444006 150444006 single base substitution C T intron_variant BRCA-EU 5 150444006 150444006 single base substitution C T upstream_gene_variant BRCA-EU 5 150444046 150444046 single base substitution C A intron_variant BRCA-EU 5 150444046 150444046 single base substitution C A upstream_gene_variant BRCA-EU 5 150444805 150444805 single base substitution T G intron_variant BRCA-EU 5 150444805 150444805 single base substitution T G upstream_gene_variant BRCA-EU 5 150445988 150445988 single base substitution A G intron_variant BRCA-EU 5 150445988 150445988 single base substitution A G upstream_gene_variant BRCA-EU 5 150450602 150450602 single base substitution G A intron_variant BRCA-EU 5 150451051 150451051 single base substitution C G intron_variant BRCA-EU 5 150453085 150453085 single base substitution T G downstream_gene_variant BRCA-EU 5 150453085 150453085 single base substitution T G intron_variant BRCA-EU 5 150453216 150453216 single base substitution A G downstream_gene_variant BRCA-EU 5 150453216 150453216 single base substitution A G intron_variant BRCA-EU 5 150453546 150453546 single base substitution G T downstream_gene_variant BRCA-EU 5 150453546 150453546 single base substitution G T intron_variant BRCA-EU 5 150455637 150455637 single base substitution C T downstream_gene_variant BRCA-EU 5 150455637 150455637 single base substitution C T intron_variant BRCA-EU 5 150457540 150457540 deletion of <=200bp T - downstream_gene_variant BRCA-EU 5 150457540 150457540 deletion of <=200bp T - intron_variant BRCA-EU 5 150458189 150458189 single base substitution C T intron_variant BRCA-EU 5 150458317 150458317 single base substitution A C intron_variant BRCA-EU 5 150460025 150460025 single base substitution G A intron_variant BRCA-EU 5 150460684 150460684 single base substitution G T 5_prime_UTR_variant BRCA-EU 5 150460684 150460684 single base substitution G T intron_variant BRCA-EU 5 150460684 150460684 single base substitution G T upstream_gene_variant BRCA-EU 5 150461629 150461629 single base substitution C T intron_variant BRCA-EU 5 150461629 150461629 single base substitution C T upstream_gene_variant BRCA-EU 5 150461943 150461943 single base substitution C T intron_variant BRCA-EU 5 150461943 150461943 single base substitution C T upstream_gene_variant BRCA-EU 5 150462956 150462956 single base substitution C G intron_variant BRCA-EU 5 150462956 150462956 single base substitution C G upstream_gene_variant BRCA-EU 5 150466040 150466040 single base substitution C T intron_variant BRCA-EU 5 150467666 150467666 single base substitution G A intron_variant BRCA-EU 5 150467666 150467666 single base substitution G A upstream_gene_variant BRCA-EU 5 150468041 150468041 single base substitution C T intron_variant BRCA-EU 5 150468041 150468041 single base substitution C T upstream_gene_variant BRCA-EU 5 150470219 150470219 single base substitution T C intron_variant BRCA-EU 5 150470219 150470219 single base substitution T C upstream_gene_variant BRCA-EU 5 150470723 150470723 single base substitution C T intron_variant BRCA-EU 5 150470723 150470723 single base substitution C T upstream_gene_variant BRCA-EU 5 150471157 150471157 single base substitution C G intron_variant BRCA-EU 5 150471157 150471157 single base substitution C G upstream_gene_variant BRCA-EU 5 150471557 150471557 single base substitution G A intron_variant BRCA-EU 5 150471557 150471557 single base substitution G A upstream_gene_variant BRCA-EU 5 150474401 150474401 single base substitution T C upstream_gene_variant BRCA-EU 5 150475714 150475714 single base substitution C G upstream_gene_variant BRCA-EU 5 150475945 150475945 single base substitution C T upstream_gene_variant BRCA-EU 5 150475996 150475996 insertion of <=200bp - T upstream_gene_variant BRCA-EU 5 150476850 150476850 single base substitution T A upstream_gene_variant BRCA-EU 5 150476859 150476859 single base substitution C T upstream_gene_variant BRCA-EU 5 150477157 150477157 single base substitution G A upstream_gene_variant BRCA-FR 5 150419265 150419265 single base substitution G A downstream_gene_variant BRCA-FR 5 150419265 150419265 single base substitution G A intron_variant BRCA-FR 5 150419265 150419265 single base substitution G A upstream_gene_variant BRCA-FR 5 150422001 150422001 single base substitution C A downstream_gene_variant BRCA-FR 5 150422001 150422001 single base substitution C A intron_variant BRCA-FR 5 150422001 150422001 single base substitution C A upstream_gene_variant BRCA-FR 5 150427376 150427376 single base substitution C T intron_variant BRCA-FR 5 150427376 150427376 single base substitution C T upstream_gene_variant BRCA-FR 5 150427655 150427655 single base substitution G C intron_variant BRCA-FR 5 150427655 150427655 single base substitution G C upstream_gene_variant BRCA-FR 5 150470723 150470723 single base substitution C T intron_variant BRCA-FR 5 150470723 150470723 single base substitution C T upstream_gene_variant BRCA-FR 5 150474401 150474401 single base substitution T C upstream_gene_variant BRCA-FR 5 150475661 150475661 single base substitution T G upstream_gene_variant BRCA-FR 5 150476859 150476859 single base substitution C T upstream_gene_variant BRCA-FR 5 150477455 150477455 single base substitution C A upstream_gene_variant BRCA-UK 5 150444046 150444046 single base substitution C A intron_variant BRCA-UK 5 150444046 150444046 single base substitution C A upstream_gene_variant BRCA-UK 5 150446597 150446597 single base substitution G A intron_variant BRCA-UK 5 150446597 150446597 single base substitution G A upstream_gene_variant BRCA-UK 5 150464792 150464792 single base substitution C G intron_variant BRCA-UK 5 150464792 150464792 single base substitution C G upstream_gene_variant BRCA-US 5 150406533 150406533 single base substitution G A downstream_gene_variant BRCA-US 5 150425443 150425443 single base substitution C T exon_variant BRCA-US 5 150425443 150425443 single base substitution C T intron_variant BRCA-US 5 150425443 150425443 single base substitution C T missense_variant M252I 756G>A BRCA-US 5 150425443 150425443 single base substitution C T missense_variant M305I 915G>A BRCA-US 5 150425460 150425460 single base substitution C T exon_variant BRCA-US 5 150425460 150425460 single base substitution C T intron_variant BRCA-US 5 150425460 150425460 single base substitution C T missense_variant E247K 739G>A BRCA-US 5 150425460 150425460 single base substitution C T missense_variant E300K 898G>A BRCA-US 5 150439923 150439923 single base substitution C T exon_variant BRCA-US 5 150439923 150439923 single base substitution C T missense_variant E131K 391G>A BRCA-US 5 150439923 150439923 single base substitution C T missense_variant E78K 232G>A BTCA-JP 5 150414691 150414691 single base substitution C T intron_variant BTCA-JP 5 150440009 150440009 single base substitution C T intron_variant CLLE-ES 5 150436102 150436102 single base substitution C A downstream_gene_variant CLLE-ES 5 150436102 150436102 single base substitution C A intron_variant CLLE-ES 5 150442702 150442702 insertion of <=200bp - TAAAGTTACGGT intron_variant CLLE-ES 5 150456813 150456814 deletion of <=200bp TA - downstream_gene_variant CLLE-ES 5 150456813 150456814 deletion of <=200bp TA - intron_variant CLLE-ES 5 150466595 150466595 single base substitution G A intron_variant COAD-US 5 150410296 150410296 deletion of <=200bp T - 3_prime_UTR_variant COAD-US 5 150410296 150410296 deletion of <=200bp T - downstream_gene_variant COAD-US 5 150410296 150410296 deletion of <=200bp T - exon_variant COAD-US 5 150410296 150410296 deletion of <=200bp T - frameshift_variant M534 COAD-US 5 150410296 150410296 deletion of <=200bp T - frameshift_variant N566 COAD-US 5 150410296 150410296 deletion of <=200bp T - frameshift_variant N577 COAD-US 5 150410296 150410296 deletion of <=200bp T - frameshift_variant N630 COAD-US 5 150410296 150410296 deletion of <=200bp T - intron_variant COAD-US 5 150411907 150411907 single base substitution C T 3_prime_UTR_variant COAD-US 5 150411907 150411907 single base substitution C T downstream_gene_variant COAD-US 5 150411907 150411907 single base substitution C T exon_variant COAD-US 5 150411907 150411907 single base substitution C T intron_variant COAD-US 5 150411907 150411907 single base substitution C T missense_variant R542Q 1625G>A COAD-US 5 150411907 150411907 single base substitution C T missense_variant R553Q 1658G>A COAD-US 5 150411907 150411907 single base substitution C T missense_variant R606Q 1817G>A COAD-US 5 150413182 150413182 single base substitution C T downstream_gene_variant COAD-US 5 150413182 150413182 single base substitution C T exon_variant COAD-US 5 150413182 150413182 single base substitution C T intron_variant COAD-US 5 150413182 150413182 single base substitution C T missense_variant R536H 1607G>A COAD-US 5 150413182 150413182 single base substitution C T missense_variant R589H 1766G>A COAD-US 5 150413227 150413227 deletion of <=200bp G - downstream_gene_variant COAD-US 5 150413227 150413227 deletion of <=200bp G - exon_variant COAD-US 5 150413227 150413227 deletion of <=200bp G - frameshift_variant P521 COAD-US 5 150413227 150413227 deletion of <=200bp G - frameshift_variant P574 COAD-US 5 150413227 150413227 deletion of <=200bp G - intron_variant COAD-US 5 150415226 150415226 single base substitution G A exon_variant COAD-US 5 150415226 150415226 single base substitution G A intron_variant COAD-US 5 150415226 150415226 single base substitution G A missense_variant R427C 1279C>T COAD-US 5 150415226 150415226 single base substitution G A missense_variant R480C 1438C>T COAD-US 5 150415226 150415226 single base substitution G A missense_variant R93C 277C>T COAD-US 5 150415226 150415226 single base substitution G A upstream_gene_variant COAD-US 5 150425467 150425467 single base substitution G A exon_variant COAD-US 5 150425467 150425467 single base substitution G A intron_variant COAD-US 5 150425467 150425467 single base substitution G A synonymous_variant G244G 732C>T COAD-US 5 150425467 150425467 single base substitution G A synonymous_variant G297G 891C>T COCA-CN 5 150410291 150410291 single base substitution G A 3_prime_UTR_variant COCA-CN 5 150410291 150410291 single base substitution G A downstream_gene_variant COCA-CN 5 150410291 150410291 single base substitution G A exon_variant COCA-CN 5 150410291 150410291 single base substitution G A intron_variant COCA-CN 5 150410291 150410291 single base substitution G A missense_variant R568C 1702C>T COCA-CN 5 150410291 150410291 single base substitution G A missense_variant R579C 1735C>T COCA-CN 5 150410291 150410291 single base substitution G A missense_variant R632C 1894C>T COCA-CN 5 150410291 150410291 single base substitution G A synonymous_variant T535T 1605C>T COCA-CN 5 150413297 150413297 single base substitution C T downstream_gene_variant COCA-CN 5 150413297 150413297 single base substitution C T exon_variant COCA-CN 5 150413297 150413297 single base substitution C T intron_variant COCA-CN 5 150413297 150413297 single base substitution C T missense_variant A498T 1492G>A COCA-CN 5 150413297 150413297 single base substitution C T missense_variant A551T 1651G>A COCA-CN 5 150415323 150415323 single base substitution C T intron_variant COCA-CN 5 150415323 150415323 single base substitution C T upstream_gene_variant COCA-CN 5 150416324 150416324 single base substitution C T intron_variant COCA-CN 5 150416324 150416324 single base substitution C T upstream_gene_variant COCA-CN 5 150416469 150416469 single base substitution G A exon_variant COCA-CN 5 150416469 150416469 single base substitution G A intron_variant COCA-CN 5 150416469 150416469 single base substitution G A missense_variant A373V 1118C>T COCA-CN 5 150416469 150416469 single base substitution G A missense_variant A39V 116C>T COCA-CN 5 150416469 150416469 single base substitution G A missense_variant A426V 1277C>T COCA-CN 5 150416469 150416469 single base substitution G A upstream_gene_variant COCA-CN 5 150422422 150422422 single base substitution A G downstream_gene_variant COCA-CN 5 150422422 150422422 single base substitution A G intron_variant COCA-CN 5 150422422 150422422 single base substitution A G upstream_gene_variant COCA-CN 5 150436326 150436326 single base substitution C T downstream_gene_variant COCA-CN 5 150436326 150436326 single base substitution C T splice_donor_variant COCA-CN 5 150439391 150439391 single base substitution T A downstream_gene_variant COCA-CN 5 150439391 150439391 single base substitution T A intron_variant COCA-CN 5 150462999 150462999 single base substitution T C intron_variant COCA-CN 5 150462999 150462999 single base substitution T C upstream_gene_variant COCA-CN 5 150470347 150470347 single base substitution G T intron_variant COCA-CN 5 150470347 150470347 single base substitution G T upstream_gene_variant EOPC-DE 5 150411284 150411284 single base substitution G A downstream_gene_variant EOPC-DE 5 150411284 150411284 single base substitution G A intron_variant EOPC-DE 5 150414150 150414150 single base substitution T G exon_variant EOPC-DE 5 150414150 150414150 single base substitution T G intron_variant EOPC-DE 5 150436472 150436472 single base substitution A C downstream_gene_variant EOPC-DE 5 150436472 150436472 single base substitution A C exon_variant EOPC-DE 5 150436472 150436472 single base substitution A C missense_variant L108R 323T>G EOPC-DE 5 150436472 150436472 single base substitution A C missense_variant L161R 482T>G EOPC-DE 5 150436652 150436652 single base substitution C A downstream_gene_variant EOPC-DE 5 150436652 150436652 single base substitution C A intron_variant EOPC-DE 5 150456285 150456285 single base substitution C T downstream_gene_variant EOPC-DE 5 150456285 150456285 single base substitution C T intron_variant EOPC-DE 5 150470065 150470065 single base substitution T A intron_variant EOPC-DE 5 150470065 150470065 single base substitution T A upstream_gene_variant ESAD-UK 5 150404722 150404722 single base substitution C T downstream_gene_variant ESAD-UK 5 150407521 150407521 single base substitution T C downstream_gene_variant ESAD-UK 5 150409977 150409977 single base substitution A G 3_prime_UTR_variant ESAD-UK 5 150409977 150409977 single base substitution A G downstream_gene_variant ESAD-UK 5 150409977 150409977 single base substitution A G intron_variant ESAD-UK 5 150417419 150417419 single base substitution G A intron_variant ESAD-UK 5 150417419 150417419 single base substitution G A upstream_gene_variant ESAD-UK 5 150420616 150420618 deletion of <=200bp CTT - downstream_gene_variant ESAD-UK 5 150420616 150420618 deletion of <=200bp CTT - intron_variant ESAD-UK 5 150420616 150420618 deletion of <=200bp CTT - upstream_gene_variant ESAD-UK 5 150423759 150423759 single base substitution A G downstream_gene_variant ESAD-UK 5 150423759 150423759 single base substitution A G intron_variant ESAD-UK 5 150423759 150423759 single base substitution A G upstream_gene_variant ESAD-UK 5 150429963 150429963 single base substitution T C intron_variant ESAD-UK 5 150429963 150429963 single base substitution T C upstream_gene_variant ESAD-UK 5 150436830 150436830 single base substitution C T downstream_gene_variant ESAD-UK 5 150436830 150436830 single base substitution C T intron_variant ESAD-UK 5 150437008 150437008 single base substitution C T downstream_gene_variant ESAD-UK 5 150437008 150437008 single base substitution C T intron_variant ESAD-UK 5 150439420 150439433 deletion of <=200bp GTGTGTGTGCGCGC - downstream_gene_variant ESAD-UK 5 150439420 150439433 deletion of <=200bp GTGTGTGTGCGCGC - intron_variant ESAD-UK 5 150439725 150439725 single base substitution G C downstream_gene_variant ESAD-UK 5 150439725 150439725 single base substitution G C intron_variant ESAD-UK 5 150444651 150444651 single base substitution T C intron_variant ESAD-UK 5 150444651 150444651 single base substitution T C synonymous_variant E2E 6A>G ESAD-UK 5 150444651 150444651 single base substitution T C upstream_gene_variant ESAD-UK 5 150445540 150445540 single base substitution T A intron_variant ESAD-UK 5 150445540 150445540 single base substitution T A upstream_gene_variant ESAD-UK 5 150447375 150447375 single base substitution G A intron_variant ESAD-UK 5 150447375 150447375 single base substitution G A upstream_gene_variant ESAD-UK 5 150447867 150447867 single base substitution G A intron_variant ESAD-UK 5 150447867 150447867 single base substitution G A upstream_gene_variant ESAD-UK 5 150449308 150449308 single base substitution C A intron_variant ESAD-UK 5 150449308 150449308 single base substitution C A upstream_gene_variant ESAD-UK 5 150451501 150451501 single base substitution G A intron_variant ESAD-UK 5 150452183 150452183 single base substitution T C intron_variant ESAD-UK 5 150456875 150456875 single base substitution T G downstream_gene_variant ESAD-UK 5 150456875 150456875 single base substitution T G intron_variant ESAD-UK 5 150457951 150457951 single base substitution C A downstream_gene_variant ESAD-UK 5 150457951 150457951 single base substitution C A intron_variant ESAD-UK 5 150463548 150463548 single base substitution G A intron_variant ESAD-UK 5 150463548 150463548 single base substitution G A upstream_gene_variant ESAD-UK 5 150464505 150464505 single base substitution T C intron_variant ESAD-UK 5 150464505 150464505 single base substitution T C upstream_gene_variant ESAD-UK 5 150465174 150465174 single base substitution C A intron_variant ESAD-UK 5 150465174 150465174 single base substitution C A upstream_gene_variant ESAD-UK 5 150468566 150468566 single base substitution G A intron_variant ESAD-UK 5 150468566 150468566 single base substitution G A upstream_gene_variant ESAD-UK 5 150471658 150471658 single base substitution A G intron_variant ESAD-UK 5 150471658 150471658 single base substitution A G upstream_gene_variant ESAD-UK 5 150472841 150472841 single base substitution C T intron_variant ESAD-UK 5 150473077 150473077 single base substitution G A 5_prime_UTR_variant ESAD-UK 5 150477883 150477883 single base substitution T A upstream_gene_variant GBM-US 5 150422129 150422131 deletion of <=200bp AGG - disruptive_inframe_deletion LL315L GBM-US 5 150422129 150422131 deletion of <=200bp AGG - disruptive_inframe_deletion LL368L GBM-US 5 150422129 150422131 deletion of <=200bp AGG - downstream_gene_variant GBM-US 5 150422129 150422131 deletion of <=200bp AGG - exon_variant GBM-US 5 150422129 150422131 deletion of <=200bp AGG - intron_variant GBM-US 5 150422129 150422131 deletion of <=200bp AGG - upstream_gene_variant KIRC-US 5 150407548 150407548 single base substitution C A downstream_gene_variant KIRC-US 5 150407659 150407659 single base substitution C T downstream_gene_variant KIRC-US 5 150422134 150422134 single base substitution G C downstream_gene_variant KIRC-US 5 150422134 150422134 single base substitution G C exon_variant KIRC-US 5 150422134 150422134 single base substitution G C intron_variant KIRC-US 5 150422134 150422134 single base substitution G C synonymous_variant L314L 942C>G KIRC-US 5 150422134 150422134 single base substitution G C synonymous_variant L367L 1101C>G KIRC-US 5 150422134 150422134 single base substitution G C upstream_gene_variant KIRP-US 5 150444534 150444534 single base substitution C G intron_variant KIRP-US 5 150444534 150444534 single base substitution C G synonymous_variant G41G 123G>C KIRP-US 5 150444534 150444534 single base substitution C G upstream_gene_variant LAML-KR 5 150413724 150413724 single base substitution A G downstream_gene_variant LAML-KR 5 150413724 150413724 single base substitution A G intron_variant LGG-US 5 150425452 150425454 deletion of <=200bp CTT - exon_variant LGG-US 5 150425452 150425454 deletion of <=200bp CTT - inframe_deletion K249 LGG-US 5 150425452 150425454 deletion of <=200bp CTT - inframe_deletion K302 LGG-US 5 150425452 150425454 deletion of <=200bp CTT - intron_variant LICA-CN 5 150416477 150416477 single base substitution C A exon_variant LICA-CN 5 150416477 150416477 single base substitution C A intron_variant LICA-CN 5 150416477 150416477 single base substitution C A synonymous_variant L36L 108G>T LICA-CN 5 150416477 150416477 single base substitution C A synonymous_variant L370L 1110G>T LICA-CN 5 150416477 150416477 single base substitution C A synonymous_variant L423L 1269G>T LICA-CN 5 150416477 150416477 single base substitution C A upstream_gene_variant LICA-FR 5 150413202 150413202 single base substitution C T downstream_gene_variant LICA-FR 5 150413202 150413202 single base substitution C T exon_variant LICA-FR 5 150413202 150413202 single base substitution C T intron_variant LICA-FR 5 150413202 150413202 single base substitution C T synonymous_variant P529P 1587G>A LICA-FR 5 150413202 150413202 single base substitution C T synonymous_variant P582P 1746G>A LICA-FR 5 150416384 150416384 single base substitution C G exon_variant LICA-FR 5 150416384 150416384 single base substitution C G intron_variant LICA-FR 5 150416384 150416384 single base substitution C G missense_variant E401D 1203G>C LICA-FR 5 150416384 150416384 single base substitution C G missense_variant E454D 1362G>C LICA-FR 5 150416384 150416384 single base substitution C G missense_variant E67D 201G>C LICA-FR 5 150416384 150416384 single base substitution C G upstream_gene_variant LICA-FR 5 150422128 150422128 single base substitution C A downstream_gene_variant LICA-FR 5 150422128 150422128 single base substitution C A exon_variant LICA-FR 5 150422128 150422128 single base substitution C A intron_variant LICA-FR 5 150422128 150422128 single base substitution C A synonymous_variant L316L 948G>T LICA-FR 5 150422128 150422128 single base substitution C A synonymous_variant L369L 1107G>T LICA-FR 5 150422128 150422128 single base substitution C A upstream_gene_variant LICA-FR 5 150430342 150430342 single base substitution C A intron_variant LICA-FR 5 150430342 150430342 single base substitution C A upstream_gene_variant LICA-FR 5 150453717 150453717 single base substitution T C downstream_gene_variant LICA-FR 5 150453717 150453717 single base substitution T C intron_variant LICA-FR 5 150455084 150455084 single base substitution C G downstream_gene_variant LICA-FR 5 150455084 150455084 single base substitution C G intron_variant LICA-FR 5 150455554 150455554 single base substitution A G downstream_gene_variant LICA-FR 5 150455554 150455554 single base substitution A G intron_variant LICA-FR 5 150458516 150458516 single base substitution G C intron_variant LIHC-US 5 150441768 150441768 single base substitution C A exon_variant LIHC-US 5 150441768 150441768 single base substitution C A missense_variant D40Y 118G>T LIHC-US 5 150441768 150441768 single base substitution C A missense_variant D93Y 277G>T LINC-JP 5 150406591 150406591 single base substitution T C downstream_gene_variant LINC-JP 5 150407602 150407602 single base substitution T G downstream_gene_variant LINC-JP 5 150409464 150409464 single base substitution G C downstream_gene_variant LINC-JP 5 150414307 150414307 single base substitution T C exon_variant LINC-JP 5 150414307 150414307 single base substitution T C intron_variant LINC-JP 5 150422154 150422154 single base substitution G A downstream_gene_variant LINC-JP 5 150422154 150422154 single base substitution G A exon_variant LINC-JP 5 150422154 150422154 single base substitution G A intron_variant LINC-JP 5 150422154 150422154 single base substitution G A missense_variant R308C 922C>T LINC-JP 5 150422154 150422154 single base substitution G A missense_variant R361C 1081C>T LINC-JP 5 150422154 150422154 single base substitution G A upstream_gene_variant LINC-JP 5 150431790 150431790 single base substitution C A exon_variant LINC-JP 5 150431790 150431790 single base substitution C A stop_gained E167* 499G>T LINC-JP 5 150431790 150431790 single base substitution C A stop_gained E220* 658G>T LINC-JP 5 150431790 150431790 single base substitution C A upstream_gene_variant LINC-JP 5 150441716 150441716 single base substitution G C exon_variant LINC-JP 5 150441716 150441716 single base substitution G C missense_variant P110R 329C>G LINC-JP 5 150441716 150441716 single base substitution G C missense_variant P57R 170C>G LINC-JP 5 150451759 150451759 single base substitution G A intron_variant LIRI-JP 5 150404564 150404564 single base substitution G C downstream_gene_variant LIRI-JP 5 150404566 150404566 single base substitution G A downstream_gene_variant LIRI-JP 5 150404877 150404877 single base substitution C T downstream_gene_variant LIRI-JP 5 150405053 150405058 deletion of <=200bp TGGTAA - downstream_gene_variant LIRI-JP 5 150412348 150412348 single base substitution G T downstream_gene_variant LIRI-JP 5 150412348 150412348 single base substitution G T exon_variant LIRI-JP 5 150412348 150412348 single base substitution G T intron_variant LIRI-JP 5 150416252 150416252 single base substitution T G intron_variant LIRI-JP 5 150416252 150416252 single base substitution T G upstream_gene_variant LIRI-JP 5 150417835 150417835 single base substitution A C downstream_gene_variant LIRI-JP 5 150417835 150417835 single base substitution A C intron_variant LIRI-JP 5 150417835 150417835 single base substitution A C upstream_gene_variant LIRI-JP 5 150418512 150418512 single base substitution G A downstream_gene_variant LIRI-JP 5 150418512 150418512 single base substitution G A intron_variant LIRI-JP 5 150418512 150418512 single base substitution G A upstream_gene_variant LIRI-JP 5 150419579 150419579 single base substitution C T downstream_gene_variant LIRI-JP 5 150419579 150419579 single base substitution C T intron_variant LIRI-JP 5 150419579 150419579 single base substitution C T upstream_gene_variant LIRI-JP 5 150422146 150422146 single base substitution A G downstream_gene_variant LIRI-JP 5 150422146 150422146 single base substitution A G exon_variant LIRI-JP 5 150422146 150422146 single base substitution A G intron_variant LIRI-JP 5 150422146 150422146 single base substitution A G synonymous_variant F310F 930T>C LIRI-JP 5 150422146 150422146 single base substitution A G synonymous_variant F363F 1089T>C LIRI-JP 5 150422146 150422146 single base substitution A G upstream_gene_variant LIRI-JP 5 150422548 150422548 single base substitution G A downstream_gene_variant LIRI-JP 5 150422548 150422548 single base substitution G A intron_variant LIRI-JP 5 150422548 150422548 single base substitution G A upstream_gene_variant LIRI-JP 5 150422917 150422917 single base substitution T C downstream_gene_variant LIRI-JP 5 150422917 150422917 single base substitution T C intron_variant LIRI-JP 5 150422917 150422917 single base substitution T C upstream_gene_variant LIRI-JP 5 150425040 150425040 single base substitution T C downstream_gene_variant LIRI-JP 5 150425040 150425040 single base substitution T C intron_variant LIRI-JP 5 150429207 150429207 single base substitution C T intron_variant LIRI-JP 5 150429207 150429207 single base substitution C T upstream_gene_variant LIRI-JP 5 150439504 150439504 single base substitution C T downstream_gene_variant LIRI-JP 5 150439504 150439504 single base substitution C T intron_variant LIRI-JP 5 150442831 150442831 single base substitution C G intron_variant LIRI-JP 5 150442963 150442963 single base substitution C A intron_variant LIRI-JP 5 150443317 150443326 deletion of <=200bp ATTGGGGAAG - intron_variant LIRI-JP 5 150443317 150443326 deletion of <=200bp ATTGGGGAAG - upstream_gene_variant LIRI-JP 5 150444188 150444189 deletion of <=200bp TC - intron_variant LIRI-JP 5 150444188 150444189 deletion of <=200bp TC - upstream_gene_variant LIRI-JP 5 150448165 150448165 single base substitution C T intron_variant LIRI-JP 5 150448165 150448165 single base substitution C T upstream_gene_variant LIRI-JP 5 150458466 150458466 single base substitution G C intron_variant LIRI-JP 5 150459831 150459831 single base substitution T C exon_variant LIRI-JP 5 150459831 150459831 single base substitution T C intron_variant LIRI-JP 5 150462432 150462432 single base substitution G T intron_variant LIRI-JP 5 150462432 150462432 single base substitution G T upstream_gene_variant LIRI-JP 5 150463301 150463302 deletion of <=200bp AG - intron_variant LIRI-JP 5 150463301 150463302 deletion of <=200bp AG - upstream_gene_variant LIRI-JP 5 150464114 150464114 single base substitution T C intron_variant LIRI-JP 5 150464114 150464114 single base substitution T C upstream_gene_variant LIRI-JP 5 150464220 150464220 single base substitution A G intron_variant LIRI-JP 5 150464220 150464220 single base substitution A G upstream_gene_variant LIRI-JP 5 150464558 150464558 single base substitution C A intron_variant LIRI-JP 5 150464558 150464558 single base substitution C A upstream_gene_variant LIRI-JP 5 150467799 150467799 single base substitution G C intron_variant LIRI-JP 5 150467799 150467799 single base substitution G C upstream_gene_variant LIRI-JP 5 150472514 150472514 single base substitution C G intron_variant LIRI-JP 5 150475205 150475205 single base substitution G A upstream_gene_variant LIRI-JP 5 150475236 150475236 single base substitution A T upstream_gene_variant LIRI-JP 5 150475702 150475702 single base substitution T A upstream_gene_variant LUSC-KR 5 150405229 150405229 single base substitution C A downstream_gene_variant LUSC-KR 5 150406372 150406372 single base substitution G A downstream_gene_variant LUSC-KR 5 150407783 150407783 single base substitution C T downstream_gene_variant LUSC-KR 5 150409477 150409477 single base substitution T C downstream_gene_variant LUSC-KR 5 150416308 150416308 single base substitution C A intron_variant LUSC-KR 5 150416308 150416308 single base substitution C A upstream_gene_variant LUSC-KR 5 150419615 150419615 single base substitution C A downstream_gene_variant LUSC-KR 5 150419615 150419615 single base substitution C A intron_variant LUSC-KR 5 150419615 150419615 single base substitution C A upstream_gene_variant LUSC-KR 5 150427674 150427674 single base substitution C G intron_variant LUSC-KR 5 150427674 150427674 single base substitution C G upstream_gene_variant LUSC-KR 5 150436230 150436230 single base substitution C A downstream_gene_variant LUSC-KR 5 150436230 150436230 single base substitution C A intron_variant LUSC-KR 5 150442725 150442725 single base substitution C A intron_variant LUSC-KR 5 150442736 150442736 single base substitution G T intron_variant LUSC-KR 5 150442908 150442908 single base substitution T C intron_variant LUSC-KR 5 150446149 150446149 single base substitution A C intron_variant LUSC-KR 5 150446149 150446149 single base substitution A C upstream_gene_variant LUSC-KR 5 150452161 150452161 single base substitution T C intron_variant LUSC-KR 5 150460726 150460726 single base substitution C T 5_prime_UTR_variant LUSC-KR 5 150460726 150460726 single base substitution C T intron_variant LUSC-KR 5 150460726 150460726 single base substitution C T upstream_gene_variant LUSC-KR 5 150464841 150464841 single base substitution G T intron_variant LUSC-KR 5 150464841 150464841 single base substitution G T upstream_gene_variant LUSC-KR 5 150465367 150465367 single base substitution C A intron_variant LUSC-KR 5 150465367 150465367 single base substitution C A upstream_gene_variant LUSC-KR 5 150466301 150466301 single base substitution A G intron_variant LUSC-KR 5 150470775 150470775 single base substitution G T intron_variant LUSC-KR 5 150470775 150470775 single base substitution G T upstream_gene_variant LUSC-KR 5 150471026 150471026 single base substitution G T intron_variant LUSC-KR 5 150471026 150471026 single base substitution G T upstream_gene_variant LUSC-KR 5 150471644 150471644 single base substitution C A intron_variant LUSC-KR 5 150471644 150471644 single base substitution C A upstream_gene_variant LUSC-KR 5 150472928 150472928 single base substitution T C intron_variant LUSC-US 5 150416412 150416412 single base substitution C A exon_variant LUSC-US 5 150416412 150416412 single base substitution C A intron_variant LUSC-US 5 150416412 150416412 single base substitution C A missense_variant G392V 1175G>T LUSC-US 5 150416412 150416412 single base substitution C A missense_variant G445V 1334G>T LUSC-US 5 150416412 150416412 single base substitution C A missense_variant G58V 173G>T LUSC-US 5 150416412 150416412 single base substitution C A upstream_gene_variant LUSC-US 5 150436437 150436437 single base substitution C T downstream_gene_variant LUSC-US 5 150436437 150436437 single base substitution C T exon_variant LUSC-US 5 150436437 150436437 single base substitution C T missense_variant E120K 358G>A LUSC-US 5 150436437 150436437 single base substitution C T missense_variant E173K 517G>A MALY-DE 5 150420735 150420735 single base substitution G A downstream_gene_variant MALY-DE 5 150420735 150420735 single base substitution G A intron_variant MALY-DE 5 150420735 150420735 single base substitution G A upstream_gene_variant MALY-DE 5 150422499 150422499 single base substitution C T downstream_gene_variant MALY-DE 5 150422499 150422499 single base substitution C T exon_variant MALY-DE 5 150422499 150422499 single base substitution C T intron_variant MALY-DE 5 150422499 150422499 single base substitution C T stop_gained W267* 801G>A MALY-DE 5 150422499 150422499 single base substitution C T stop_gained W320* 960G>A MALY-DE 5 150422499 150422499 single base substitution C T upstream_gene_variant MALY-DE 5 150423919 150423919 single base substitution A G downstream_gene_variant MALY-DE 5 150423919 150423919 single base substitution A G intron_variant MALY-DE 5 150426271 150426271 single base substitution A G intron_variant MALY-DE 5 150426271 150426271 single base substitution A G upstream_gene_variant MALY-DE 5 150427711 150427711 single base substitution C T intron_variant MALY-DE 5 150427711 150427711 single base substitution C T upstream_gene_variant MALY-DE 5 150427960 150427960 single base substitution A G intron_variant MALY-DE 5 150427960 150427960 single base substitution A G upstream_gene_variant MALY-DE 5 150428001 150428001 single base substitution G C intron_variant MALY-DE 5 150428001 150428001 single base substitution G C upstream_gene_variant MALY-DE 5 150433858 150433858 single base substitution T G intron_variant MALY-DE 5 150433858 150433858 single base substitution T G upstream_gene_variant MALY-DE 5 150453144 150453145 deletion of <=200bp TG - downstream_gene_variant MALY-DE 5 150453144 150453145 deletion of <=200bp TG - intron_variant MALY-DE 5 150453586 150453586 single base substitution T A downstream_gene_variant MALY-DE 5 150453586 150453586 single base substitution T A intron_variant MALY-DE 5 150459211 150459211 single base substitution C G intron_variant MALY-DE 5 150468335 150468335 single base substitution G C intron_variant MALY-DE 5 150468335 150468335 single base substitution G C upstream_gene_variant MALY-DE 5 150468374 150468374 single base substitution T G intron_variant MALY-DE 5 150468374 150468374 single base substitution T G upstream_gene_variant MALY-DE 5 150473976 150473976 single base substitution C A upstream_gene_variant MALY-DE 5 150474808 150474809 deletion of <=200bp AC - upstream_gene_variant MELA-AU 5 150404748 150404748 single base substitution G A downstream_gene_variant MELA-AU 5 150405331 150405331 single base substitution C T downstream_gene_variant MELA-AU 5 150405882 150405882 single base substitution G T downstream_gene_variant MELA-AU 5 150406515 150406515 single base substitution T C downstream_gene_variant MELA-AU 5 150406516 150406516 single base substitution T C downstream_gene_variant MELA-AU 5 150407415 150407415 single base substitution G A downstream_gene_variant MELA-AU 5 150407426 150407426 single base substitution G A downstream_gene_variant MELA-AU 5 150407553 150407553 single base substitution G A downstream_gene_variant MELA-AU 5 150407585 150407585 single base substitution G A downstream_gene_variant MELA-AU 5 150407727 150407727 single base substitution G A downstream_gene_variant MELA-AU 5 150407927 150407927 single base substitution G A downstream_gene_variant MELA-AU 5 150408043 150408043 single base substitution G A downstream_gene_variant MELA-AU 5 150408737 150408737 single base substitution C T downstream_gene_variant MELA-AU 5 150409013 150409013 single base substitution A T downstream_gene_variant MELA-AU 5 150409047 150409047 single base substitution A G downstream_gene_variant MELA-AU 5 150409228 150409228 single base substitution G A downstream_gene_variant MELA-AU 5 150409413 150409414 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 5 150409469 150409469 single base substitution G A downstream_gene_variant MELA-AU 5 150409471 150409471 single base substitution G A downstream_gene_variant MELA-AU 5 150409616 150409616 single base substitution T C 3_prime_UTR_variant MELA-AU 5 150409616 150409616 single base substitution T C downstream_gene_variant MELA-AU 5 150409921 150409922 multiple base substitution (>=2bp and <=200bp) GG AA 3_prime_UTR_variant MELA-AU 5 150409921 150409922 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 5 150409921 150409922 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 5 150410385 150410385 single base substitution C A downstream_gene_variant MELA-AU 5 150410385 150410385 single base substitution C A intron_variant MELA-AU 5 150410904 150410904 single base substitution G A downstream_gene_variant MELA-AU 5 150410904 150410904 single base substitution G A intron_variant MELA-AU 5 150411007 150411007 single base substitution G A downstream_gene_variant MELA-AU 5 150411007 150411007 single base substitution G A intron_variant MELA-AU 5 150411795 150411795 single base substitution G A downstream_gene_variant MELA-AU 5 150411795 150411795 single base substitution G A exon_variant MELA-AU 5 150411795 150411795 single base substitution G A intron_variant MELA-AU 5 150412111 150412111 single base substitution G A downstream_gene_variant MELA-AU 5 150412111 150412111 single base substitution G A exon_variant MELA-AU 5 150412111 150412111 single base substitution G A intron_variant MELA-AU 5 150412840 150412840 single base substitution G A downstream_gene_variant MELA-AU 5 150412840 150412840 single base substitution G A intron_variant MELA-AU 5 150412940 150412940 single base substitution C T downstream_gene_variant MELA-AU 5 150412940 150412940 single base substitution C T intron_variant MELA-AU 5 150413259 150413259 single base substitution G A downstream_gene_variant MELA-AU 5 150413259 150413259 single base substitution G A exon_variant MELA-AU 5 150413259 150413259 single base substitution G A intron_variant MELA-AU 5 150413259 150413259 single base substitution G A synonymous_variant G510G 1530C>T MELA-AU 5 150413259 150413259 single base substitution G A synonymous_variant G563G 1689C>T MELA-AU 5 150413407 150413407 single base substitution A T downstream_gene_variant MELA-AU 5 150413407 150413407 single base substitution A T intron_variant MELA-AU 5 150413872 150413872 single base substitution G A downstream_gene_variant MELA-AU 5 150413872 150413872 single base substitution G A intron_variant MELA-AU 5 150414108 150414109 multiple base substitution (>=2bp and <=200bp) GG AC exon_variant MELA-AU 5 150414108 150414109 multiple base substitution (>=2bp and <=200bp) GG AC intron_variant MELA-AU 5 150414124 150414124 single base substitution G A exon_variant MELA-AU 5 150414124 150414124 single base substitution G A intron_variant MELA-AU 5 150415226 150415226 single base substitution G A exon_variant MELA-AU 5 150415226 150415226 single base substitution G A intron_variant MELA-AU 5 150415226 150415226 single base substitution G A missense_variant R427C 1279C>T MELA-AU 5 150415226 150415226 single base substitution G A missense_variant R480C 1438C>T MELA-AU 5 150415226 150415226 single base substitution G A missense_variant R93C 277C>T MELA-AU 5 150415226 150415226 single base substitution G A upstream_gene_variant MELA-AU 5 150415577 150415577 single base substitution G A intron_variant MELA-AU 5 150415577 150415577 single base substitution G A upstream_gene_variant MELA-AU 5 150415613 150415613 single base substitution G A intron_variant MELA-AU 5 150415613 150415613 single base substitution G A upstream_gene_variant MELA-AU 5 150416042 150416042 single base substitution C T intron_variant MELA-AU 5 150416042 150416042 single base substitution C T upstream_gene_variant MELA-AU 5 150416390 150416390 single base substitution T C exon_variant MELA-AU 5 150416390 150416390 single base substitution T C intron_variant MELA-AU 5 150416390 150416390 single base substitution T C synonymous_variant K399K 1197A>G MELA-AU 5 150416390 150416390 single base substitution T C synonymous_variant K452K 1356A>G MELA-AU 5 150416390 150416390 single base substitution T C synonymous_variant K65K 195A>G MELA-AU 5 150416390 150416390 single base substitution T C upstream_gene_variant MELA-AU 5 150416392 150416392 single base substitution T A exon_variant MELA-AU 5 150416392 150416392 single base substitution T A intron_variant MELA-AU 5 150416392 150416392 single base substitution T A stop_gained K399* 1195A>T MELA-AU 5 150416392 150416392 single base substitution T A stop_gained K452* 1354A>T MELA-AU 5 150416392 150416392 single base substitution T A stop_gained K65* 193A>T MELA-AU 5 150416392 150416392 single base substitution T A upstream_gene_variant MELA-AU 5 150416540 150416540 single base substitution G A exon_variant MELA-AU 5 150416540 150416540 single base substitution G A intron_variant MELA-AU 5 150416540 150416540 single base substitution G A upstream_gene_variant MELA-AU 5 150416725 150416725 single base substitution A C exon_variant MELA-AU 5 150416725 150416725 single base substitution A C intron_variant MELA-AU 5 150416725 150416725 single base substitution A C upstream_gene_variant MELA-AU 5 150416856 150416856 single base substitution G A exon_variant MELA-AU 5 150416856 150416856 single base substitution G A intron_variant MELA-AU 5 150416856 150416856 single base substitution G A upstream_gene_variant MELA-AU 5 150416922 150416922 single base substitution A G exon_variant MELA-AU 5 150416922 150416922 single base substitution A G intron_variant MELA-AU 5 150416922 150416922 single base substitution A G upstream_gene_variant MELA-AU 5 150417786 150417786 single base substitution G A downstream_gene_variant MELA-AU 5 150417786 150417786 single base substitution G A intron_variant MELA-AU 5 150417786 150417786 single base substitution G A upstream_gene_variant MELA-AU 5 150417864 150417864 single base substitution G A downstream_gene_variant MELA-AU 5 150417864 150417864 single base substitution G A intron_variant MELA-AU 5 150417864 150417864 single base substitution G A upstream_gene_variant MELA-AU 5 150419629 150419629 single base substitution C A downstream_gene_variant MELA-AU 5 150419629 150419629 single base substitution C A intron_variant MELA-AU 5 150419629 150419629 single base substitution C A upstream_gene_variant MELA-AU 5 150419814 150419814 single base substitution G A downstream_gene_variant MELA-AU 5 150419814 150419814 single base substitution G A intron_variant MELA-AU 5 150419814 150419814 single base substitution G A upstream_gene_variant MELA-AU 5 150419840 150419840 single base substitution G A downstream_gene_variant MELA-AU 5 150419840 150419840 single base substitution G A intron_variant MELA-AU 5 150419840 150419840 single base substitution G A upstream_gene_variant MELA-AU 5 150420084 150420084 single base substitution G A downstream_gene_variant MELA-AU 5 150420084 150420084 single base substitution G A intron_variant MELA-AU 5 150420084 150420084 single base substitution G A upstream_gene_variant MELA-AU 5 150420735 150420735 single base substitution G T downstream_gene_variant MELA-AU 5 150420735 150420735 single base substitution G T intron_variant MELA-AU 5 150420735 150420735 single base substitution G T upstream_gene_variant MELA-AU 5 150421019 150421019 single base substitution A G downstream_gene_variant MELA-AU 5 150421019 150421019 single base substitution A G intron_variant MELA-AU 5 150421019 150421019 single base substitution A G upstream_gene_variant MELA-AU 5 150421693 150421693 single base substitution G A downstream_gene_variant MELA-AU 5 150421693 150421693 single base substitution G A intron_variant MELA-AU 5 150421693 150421693 single base substitution G A upstream_gene_variant MELA-AU 5 150421817 150421817 single base substitution G A downstream_gene_variant MELA-AU 5 150421817 150421817 single base substitution G A intron_variant MELA-AU 5 150421817 150421817 single base substitution G A upstream_gene_variant MELA-AU 5 150422442 150422442 single base substitution G A downstream_gene_variant MELA-AU 5 150422442 150422442 single base substitution G A intron_variant MELA-AU 5 150422442 150422442 single base substitution G A upstream_gene_variant MELA-AU 5 150423429 150423429 single base substitution G A downstream_gene_variant MELA-AU 5 150423429 150423429 single base substitution G A intron_variant MELA-AU 5 150423429 150423429 single base substitution G A upstream_gene_variant MELA-AU 5 150423525 150423525 single base substitution G A downstream_gene_variant MELA-AU 5 150423525 150423525 single base substitution G A intron_variant MELA-AU 5 150423525 150423525 single base substitution G A upstream_gene_variant MELA-AU 5 150423675 150423675 single base substitution G A downstream_gene_variant MELA-AU 5 150423675 150423675 single base substitution G A intron_variant MELA-AU 5 150423675 150423675 single base substitution G A upstream_gene_variant MELA-AU 5 150424056 150424056 single base substitution G A downstream_gene_variant MELA-AU 5 150424056 150424056 single base substitution G A intron_variant MELA-AU 5 150424595 150424595 single base substitution A G downstream_gene_variant MELA-AU 5 150424595 150424595 single base substitution A G intron_variant MELA-AU 5 150425011 150425011 single base substitution G A downstream_gene_variant MELA-AU 5 150425011 150425011 single base substitution G A intron_variant MELA-AU 5 150425228 150425228 single base substitution G A downstream_gene_variant MELA-AU 5 150425228 150425228 single base substitution G A intron_variant MELA-AU 5 150425994 150425994 single base substitution G A intron_variant MELA-AU 5 150425994 150425994 single base substitution G A upstream_gene_variant MELA-AU 5 150426930 150426930 single base substitution A G intron_variant MELA-AU 5 150426930 150426930 single base substitution A G upstream_gene_variant MELA-AU 5 150427611 150427611 single base substitution G A intron_variant MELA-AU 5 150427611 150427611 single base substitution G A upstream_gene_variant MELA-AU 5 150427749 150427749 single base substitution G A intron_variant MELA-AU 5 150427749 150427749 single base substitution G A upstream_gene_variant MELA-AU 5 150427803 150427804 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 5 150427803 150427804 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 5 150427858 150427858 single base substitution C A intron_variant MELA-AU 5 150427858 150427858 single base substitution C A upstream_gene_variant MELA-AU 5 150428027 150428027 single base substitution G A intron_variant MELA-AU 5 150428027 150428027 single base substitution G A upstream_gene_variant MELA-AU 5 150428190 150428190 single base substitution G A intron_variant MELA-AU 5 150428190 150428190 single base substitution G A upstream_gene_variant MELA-AU 5 150429826 150429826 single base substitution T A intron_variant MELA-AU 5 150429826 150429826 single base substitution T A upstream_gene_variant MELA-AU 5 150429855 150429855 single base substitution G A intron_variant MELA-AU 5 150429855 150429855 single base substitution G A upstream_gene_variant MELA-AU 5 150430651 150430651 single base substitution G A intron_variant MELA-AU 5 150430651 150430651 single base substitution G A upstream_gene_variant MELA-AU 5 150431050 150431050 single base substitution A C intron_variant MELA-AU 5 150431050 150431050 single base substitution A C upstream_gene_variant MELA-AU 5 150431069 150431069 single base substitution G A intron_variant MELA-AU 5 150431069 150431069 single base substitution G A upstream_gene_variant MELA-AU 5 150431347 150431347 single base substitution G A intron_variant MELA-AU 5 150431347 150431347 single base substitution G A upstream_gene_variant MELA-AU 5 150432022 150432022 single base substitution G T intron_variant MELA-AU 5 150432022 150432022 single base substitution G T upstream_gene_variant MELA-AU 5 150432438 150432438 single base substitution G A intron_variant MELA-AU 5 150432438 150432438 single base substitution G A upstream_gene_variant MELA-AU 5 150432471 150432471 single base substitution G A intron_variant MELA-AU 5 150432471 150432471 single base substitution G A upstream_gene_variant MELA-AU 5 150433214 150433214 single base substitution C T intron_variant MELA-AU 5 150433214 150433214 single base substitution C T upstream_gene_variant MELA-AU 5 150433763 150433763 single base substitution G A intron_variant MELA-AU 5 150433763 150433763 single base substitution G A upstream_gene_variant MELA-AU 5 150434260 150434260 single base substitution G A intron_variant MELA-AU 5 150434260 150434260 single base substitution G A upstream_gene_variant MELA-AU 5 150434713 150434713 single base substitution G A intron_variant MELA-AU 5 150434846 150434846 single base substitution G A intron_variant MELA-AU 5 150435160 150435160 single base substitution G A downstream_gene_variant MELA-AU 5 150435160 150435160 single base substitution G A intron_variant MELA-AU 5 150435480 150435481 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 5 150435480 150435481 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 5 150435763 150435763 single base substitution G A downstream_gene_variant MELA-AU 5 150435763 150435763 single base substitution G A intron_variant MELA-AU 5 150435956 150435956 insertion of <=200bp - TGTGAAGTA downstream_gene_variant MELA-AU 5 150435956 150435956 insertion of <=200bp - TGTGAAGTA intron_variant MELA-AU 5 150435992 150435992 single base substitution G A downstream_gene_variant MELA-AU 5 150435992 150435992 single base substitution G A intron_variant MELA-AU 5 150435993 150435993 single base substitution G A downstream_gene_variant MELA-AU 5 150435993 150435993 single base substitution G A intron_variant MELA-AU 5 150437205 150437205 single base substitution G A downstream_gene_variant MELA-AU 5 150437205 150437205 single base substitution G A intron_variant MELA-AU 5 150437523 150437524 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 5 150437523 150437524 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 5 150437562 150437562 single base substitution A G downstream_gene_variant MELA-AU 5 150437562 150437562 single base substitution A G intron_variant MELA-AU 5 150437617 150437617 single base substitution G A downstream_gene_variant MELA-AU 5 150437617 150437617 single base substitution G A intron_variant MELA-AU 5 150439990 150439990 single base substitution G A intron_variant MELA-AU 5 150441548 150441548 single base substitution G A intron_variant MELA-AU 5 150441808 150441809 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 5 150441861 150441861 single base substitution G A intron_variant MELA-AU 5 150442262 150442262 single base substitution G A intron_variant MELA-AU 5 150442522 150442522 single base substitution G A intron_variant MELA-AU 5 150442770 150442770 single base substitution G A intron_variant MELA-AU 5 150442773 150442773 single base substitution C G intron_variant MELA-AU 5 150442776 150442776 single base substitution G A intron_variant MELA-AU 5 150443543 150443543 single base substitution A T intron_variant MELA-AU 5 150443543 150443543 single base substitution A T upstream_gene_variant MELA-AU 5 150443825 150443825 single base substitution G A intron_variant MELA-AU 5 150443825 150443825 single base substitution G A upstream_gene_variant MELA-AU 5 150443828 150443828 single base substitution G A intron_variant MELA-AU 5 150443828 150443828 single base substitution G A upstream_gene_variant MELA-AU 5 150443887 150443887 single base substitution G A intron_variant MELA-AU 5 150443887 150443887 single base substitution G A upstream_gene_variant MELA-AU 5 150443904 150443904 single base substitution A G intron_variant MELA-AU 5 150443904 150443904 single base substitution A G upstream_gene_variant MELA-AU 5 150444093 150444093 single base substitution G A intron_variant MELA-AU 5 150444093 150444093 single base substitution G A upstream_gene_variant MELA-AU 5 150444354 150444354 single base substitution G A intron_variant MELA-AU 5 150444354 150444354 single base substitution G A upstream_gene_variant MELA-AU 5 150444460 150444460 single base substitution G A intron_variant MELA-AU 5 150444460 150444460 single base substitution G A upstream_gene_variant MELA-AU 5 150445017 150445017 single base substitution C T intron_variant MELA-AU 5 150445017 150445017 single base substitution C T upstream_gene_variant MELA-AU 5 150445755 150445755 single base substitution C T intron_variant MELA-AU 5 150445755 150445755 single base substitution C T upstream_gene_variant MELA-AU 5 150445963 150445963 single base substitution G A intron_variant MELA-AU 5 150445963 150445963 single base substitution G A upstream_gene_variant MELA-AU 5 150447102 150447103 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 5 150447102 150447103 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 5 150448557 150448557 single base substitution G A intron_variant MELA-AU 5 150448557 150448557 single base substitution G A upstream_gene_variant MELA-AU 5 150448883 150448883 single base substitution G A intron_variant MELA-AU 5 150448883 150448883 single base substitution G A upstream_gene_variant MELA-AU 5 150448891 150448891 single base substitution C A intron_variant MELA-AU 5 150448891 150448891 single base substitution C A upstream_gene_variant MELA-AU 5 150449501 150449501 single base substitution G A intron_variant MELA-AU 5 150449501 150449501 single base substitution G A upstream_gene_variant MELA-AU 5 150449529 150449529 single base substitution G C intron_variant MELA-AU 5 150449529 150449529 single base substitution G C upstream_gene_variant MELA-AU 5 150449950 150449950 single base substitution G A intron_variant MELA-AU 5 150451624 150451625 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 5 150451969 150451969 single base substitution A G intron_variant MELA-AU 5 150452302 150452302 single base substitution G A intron_variant MELA-AU 5 150452760 150452760 single base substitution G A intron_variant MELA-AU 5 150453186 150453186 single base substitution G A downstream_gene_variant MELA-AU 5 150453186 150453186 single base substitution G A intron_variant MELA-AU 5 150454043 150454043 single base substitution G A downstream_gene_variant MELA-AU 5 150454043 150454043 single base substitution G A intron_variant MELA-AU 5 150454682 150454682 single base substitution G A downstream_gene_variant MELA-AU 5 150454682 150454682 single base substitution G A intron_variant MELA-AU 5 150455670 150455670 single base substitution C T downstream_gene_variant MELA-AU 5 150455670 150455670 single base substitution C T intron_variant MELA-AU 5 150456061 150456061 single base substitution G A downstream_gene_variant MELA-AU 5 150456061 150456061 single base substitution G A intron_variant MELA-AU 5 150456514 150456514 single base substitution G A downstream_gene_variant MELA-AU 5 150456514 150456514 single base substitution G A intron_variant MELA-AU 5 150458977 150458977 single base substitution G A intron_variant MELA-AU 5 150459609 150459609 single base substitution C T intron_variant MELA-AU 5 150460267 150460267 single base substitution T A intron_variant MELA-AU 5 150461558 150461558 single base substitution G A intron_variant MELA-AU 5 150461558 150461558 single base substitution G A upstream_gene_variant MELA-AU 5 150462351 150462351 single base substitution C T intron_variant MELA-AU 5 150462351 150462351 single base substitution C T upstream_gene_variant MELA-AU 5 150462584 150462584 single base substitution C A intron_variant MELA-AU 5 150462584 150462584 single base substitution C A upstream_gene_variant MELA-AU 5 150463460 150463460 single base substitution C T intron_variant MELA-AU 5 150463460 150463460 single base substitution C T upstream_gene_variant MELA-AU 5 150463473 150463473 single base substitution C T intron_variant MELA-AU 5 150463473 150463473 single base substitution C T upstream_gene_variant MELA-AU 5 150463920 150463920 single base substitution C T intron_variant MELA-AU 5 150463920 150463920 single base substitution C T upstream_gene_variant MELA-AU 5 150464116 150464116 single base substitution G A intron_variant MELA-AU 5 150464116 150464116 single base substitution G A upstream_gene_variant MELA-AU 5 150464136 150464136 single base substitution G A intron_variant MELA-AU 5 150464136 150464136 single base substitution G A upstream_gene_variant MELA-AU 5 150464584 150464584 single base substitution C T intron_variant MELA-AU 5 150464584 150464584 single base substitution C T upstream_gene_variant MELA-AU 5 150465224 150465224 single base substitution G A intron_variant MELA-AU 5 150465224 150465224 single base substitution G A upstream_gene_variant MELA-AU 5 150465380 150465380 single base substitution C A intron_variant MELA-AU 5 150465380 150465380 single base substitution C A upstream_gene_variant MELA-AU 5 150465529 150465529 single base substitution C T intron_variant MELA-AU 5 150465529 150465529 single base substitution C T upstream_gene_variant MELA-AU 5 150466057 150466057 single base substitution G A intron_variant MELA-AU 5 150466213 150466213 single base substitution G A intron_variant MELA-AU 5 150466298 150466298 single base substitution G A intron_variant MELA-AU 5 150466420 150466420 single base substitution G A intron_variant MELA-AU 5 150466625 150466625 single base substitution G A intron_variant MELA-AU 5 150466670 150466670 single base substitution G A 5_prime_UTR_variant MELA-AU 5 150466670 150466670 single base substitution G A intron_variant MELA-AU 5 150466736 150466736 single base substitution G A intron_variant MELA-AU 5 150466736 150466736 single base substitution G A upstream_gene_variant MELA-AU 5 150467131 150467131 single base substitution C T intron_variant MELA-AU 5 150467131 150467131 single base substitution C T upstream_gene_variant MELA-AU 5 150467323 150467323 single base substitution G A intron_variant MELA-AU 5 150467323 150467323 single base substitution G A upstream_gene_variant MELA-AU 5 150467536 150467536 single base substitution G A intron_variant MELA-AU 5 150467536 150467536 single base substitution G A upstream_gene_variant MELA-AU 5 150468145 150468145 single base substitution G A intron_variant MELA-AU 5 150468145 150468145 single base substitution G A upstream_gene_variant MELA-AU 5 150468373 150468373 single base substitution A G intron_variant MELA-AU 5 150468373 150468373 single base substitution A G upstream_gene_variant MELA-AU 5 150468448 150468448 single base substitution G A intron_variant MELA-AU 5 150468448 150468448 single base substitution G A upstream_gene_variant MELA-AU 5 150469492 150469492 single base substitution G A intron_variant MELA-AU 5 150469492 150469492 single base substitution G A upstream_gene_variant MELA-AU 5 150469528 150469528 single base substitution G A intron_variant MELA-AU 5 150469528 150469528 single base substitution G A upstream_gene_variant MELA-AU 5 150469688 150469688 single base substitution G A intron_variant MELA-AU 5 150469688 150469688 single base substitution G A upstream_gene_variant MELA-AU 5 150469950 150469950 single base substitution A G intron_variant MELA-AU 5 150469950 150469950 single base substitution A G upstream_gene_variant MELA-AU 5 150469953 150469953 single base substitution A G intron_variant MELA-AU 5 150469953 150469953 single base substitution A G upstream_gene_variant MELA-AU 5 150470116 150470116 single base substitution G A intron_variant MELA-AU 5 150470116 150470116 single base substitution G A upstream_gene_variant MELA-AU 5 150470185 150470185 single base substitution C T intron_variant MELA-AU 5 150470185 150470185 single base substitution C T upstream_gene_variant MELA-AU 5 150470297 150470297 single base substitution G A intron_variant MELA-AU 5 150470297 150470297 single base substitution G A upstream_gene_variant MELA-AU 5 150470347 150470347 single base substitution G A intron_variant MELA-AU 5 150470347 150470347 single base substitution G A upstream_gene_variant MELA-AU 5 150470489 150470489 single base substitution C G intron_variant MELA-AU 5 150470489 150470489 single base substitution C G upstream_gene_variant MELA-AU 5 150470868 150470868 single base substitution T C intron_variant MELA-AU 5 150470868 150470868 single base substitution T C upstream_gene_variant MELA-AU 5 150470925 150470925 single base substitution G C intron_variant MELA-AU 5 150470925 150470925 single base substitution G C upstream_gene_variant MELA-AU 5 150471055 150471055 single base substitution C T intron_variant MELA-AU 5 150471055 150471055 single base substitution C T upstream_gene_variant MELA-AU 5 150471359 150471359 single base substitution G A intron_variant MELA-AU 5 150471359 150471359 single base substitution G A upstream_gene_variant MELA-AU 5 150471623 150471623 single base substitution T A intron_variant MELA-AU 5 150471623 150471623 single base substitution T A upstream_gene_variant MELA-AU 5 150471706 150471706 single base substitution G A intron_variant MELA-AU 5 150471706 150471706 single base substitution G A upstream_gene_variant MELA-AU 5 150471851 150471851 single base substitution G A intron_variant MELA-AU 5 150471851 150471851 single base substitution G A upstream_gene_variant MELA-AU 5 150472609 150472609 single base substitution T C intron_variant MELA-AU 5 150472957 150472957 single base substitution T G intron_variant MELA-AU 5 150473651 150473651 single base substitution G A upstream_gene_variant MELA-AU 5 150474335 150474335 single base substitution G A upstream_gene_variant MELA-AU 5 150474613 150474613 single base substitution G C upstream_gene_variant MELA-AU 5 150474980 150474980 single base substitution T A upstream_gene_variant MELA-AU 5 150475012 150475012 single base substitution A G upstream_gene_variant MELA-AU 5 150475080 150475080 single base substitution G A upstream_gene_variant MELA-AU 5 150475403 150475403 single base substitution C A upstream_gene_variant MELA-AU 5 150475607 150475607 single base substitution G A upstream_gene_variant MELA-AU 5 150477155 150477155 single base substitution G A upstream_gene_variant MELA-AU 5 150477564 150477564 single base substitution G A upstream_gene_variant ORCA-IN 5 150436453 150436453 single base substitution C T downstream_gene_variant ORCA-IN 5 150436453 150436453 single base substitution C T exon_variant ORCA-IN 5 150436453 150436453 single base substitution C T synonymous_variant T114T 342G>A ORCA-IN 5 150436453 150436453 single base substitution C T synonymous_variant T167T 501G>A ORCA-IN 5 150458272 150458272 single base substitution G A intron_variant ORCA-IN 5 150461340 150461340 single base substitution G T intron_variant ORCA-IN 5 150461340 150461340 single base substitution G T upstream_gene_variant ORCA-IN 5 150469465 150469465 single base substitution A T intron_variant ORCA-IN 5 150469465 150469465 single base substitution A T upstream_gene_variant ORCA-IN 5 150473386 150473386 single base substitution C G upstream_gene_variant OV-AU 5 150414203 150414203 single base substitution G A exon_variant OV-AU 5 150414203 150414203 single base substitution G A intron_variant OV-AU 5 150414906 150414906 single base substitution G C intron_variant OV-AU 5 150421425 150421425 single base substitution A G downstream_gene_variant OV-AU 5 150421425 150421425 single base substitution A G intron_variant OV-AU 5 150421425 150421425 single base substitution A G upstream_gene_variant OV-AU 5 150421682 150421682 single base substitution A G downstream_gene_variant OV-AU 5 150421682 150421682 single base substitution A G intron_variant OV-AU 5 150421682 150421682 single base substitution A G upstream_gene_variant OV-AU 5 150426098 150426098 single base substitution C T intron_variant OV-AU 5 150426098 150426098 single base substitution C T upstream_gene_variant OV-AU 5 150430179 150430179 single base substitution G A intron_variant OV-AU 5 150430179 150430179 single base substitution G A upstream_gene_variant OV-AU 5 150447179 150447179 single base substitution C T intron_variant OV-AU 5 150447179 150447179 single base substitution C T upstream_gene_variant OV-AU 5 150453693 150453693 single base substitution A C downstream_gene_variant OV-AU 5 150453693 150453693 single base substitution A C intron_variant OV-AU 5 150459820 150459820 single base substitution C T exon_variant OV-AU 5 150459820 150459820 single base substitution C T intron_variant OV-AU 5 150464043 150464043 single base substitution A T intron_variant OV-AU 5 150464043 150464043 single base substitution A T upstream_gene_variant OV-AU 5 150466840 150466840 single base substitution G A intron_variant OV-AU 5 150466840 150466840 single base substitution G A upstream_gene_variant OV-AU 5 150469352 150469352 single base substitution C T intron_variant OV-AU 5 150469352 150469352 single base substitution C T upstream_gene_variant OV-AU 5 150473441 150473441 single base substitution G T upstream_gene_variant OV-AU 5 150473922 150473922 single base substitution C A upstream_gene_variant OV-AU 5 150473939 150473939 single base substitution A T upstream_gene_variant OV-AU 5 150475602 150475602 single base substitution C T upstream_gene_variant PACA-AU 5 150407618 150407618 single base substitution C T downstream_gene_variant PACA-AU 5 150408174 150408174 single base substitution G A downstream_gene_variant PACA-AU 5 150408385 150408385 single base substitution G A downstream_gene_variant PACA-AU 5 150409670 150409670 single base substitution C T 3_prime_UTR_variant PACA-AU 5 150409670 150409670 single base substitution C T downstream_gene_variant PACA-AU 5 150409670 150409670 single base substitution C T synonymous_variant T134T 402G>A PACA-AU 5 150413639 150413639 single base substitution C T downstream_gene_variant PACA-AU 5 150413639 150413639 single base substitution C T intron_variant PACA-AU 5 150414467 150414467 single base substitution T C exon_variant PACA-AU 5 150414467 150414467 single base substitution T C intron_variant PACA-AU 5 150430215 150430215 single base substitution G C intron_variant PACA-AU 5 150430215 150430215 single base substitution G C upstream_gene_variant PACA-AU 5 150431834 150431834 single base substitution G T intron_variant PACA-AU 5 150431834 150431834 single base substitution G T upstream_gene_variant PACA-AU 5 150438439 150438439 single base substitution C T downstream_gene_variant PACA-AU 5 150438439 150438439 single base substitution C T intron_variant PACA-AU 5 150453309 150453309 single base substitution A G downstream_gene_variant PACA-AU 5 150453309 150453309 single base substitution A G intron_variant PACA-AU 5 150456387 150456387 single base substitution G A downstream_gene_variant PACA-AU 5 150456387 150456387 single base substitution G A intron_variant PACA-AU 5 150456848 150456848 single base substitution G A downstream_gene_variant PACA-AU 5 150456848 150456848 single base substitution G A intron_variant PACA-AU 5 150472439 150472439 single base substitution T G intron_variant PACA-AU 5 150473927 150473927 single base substitution C A upstream_gene_variant PACA-AU 5 150474252 150474252 single base substitution A G upstream_gene_variant PACA-AU 5 150475765 150475765 single base substitution C A upstream_gene_variant PACA-CA 5 150404572 150404572 single base substitution G A downstream_gene_variant PACA-CA 5 150408443 150408443 insertion of <=200bp - G downstream_gene_variant PACA-CA 5 150410007 150410007 single base substitution C T 3_prime_UTR_variant PACA-CA 5 150410007 150410007 single base substitution C T downstream_gene_variant PACA-CA 5 150410007 150410007 single base substitution C T intron_variant PACA-CA 5 150414287 150414287 single base substitution A G exon_variant PACA-CA 5 150414287 150414287 single base substitution A G intron_variant PACA-CA 5 150417436 150417436 single base substitution C T intron_variant PACA-CA 5 150417436 150417436 single base substitution C T upstream_gene_variant PACA-CA 5 150423948 150423948 single base substitution G A downstream_gene_variant PACA-CA 5 150423948 150423948 single base substitution G A intron_variant PACA-CA 5 150424064 150424064 insertion of <=200bp - A downstream_gene_variant PACA-CA 5 150424064 150424064 insertion of <=200bp - A intron_variant PACA-CA 5 150426087 150426087 single base substitution C A intron_variant PACA-CA 5 150426087 150426087 single base substitution C A upstream_gene_variant PACA-CA 5 150430205 150430205 deletion of <=200bp T - intron_variant PACA-CA 5 150430205 150430205 deletion of <=200bp T - upstream_gene_variant PACA-CA 5 150438414 150438414 single base substitution A T downstream_gene_variant PACA-CA 5 150438414 150438414 single base substitution A T intron_variant PACA-CA 5 150438451 150438451 single base substitution C G downstream_gene_variant PACA-CA 5 150438451 150438451 single base substitution C G intron_variant PACA-CA 5 150445442 150445442 single base substitution G C intron_variant PACA-CA 5 150445442 150445442 single base substitution G C upstream_gene_variant PACA-CA 5 150445462 150445462 single base substitution A T intron_variant PACA-CA 5 150445462 150445462 single base substitution A T upstream_gene_variant PACA-CA 5 150445464 150445464 single base substitution T G intron_variant PACA-CA 5 150445464 150445464 single base substitution T G upstream_gene_variant PACA-CA 5 150447395 150447395 single base substitution C T intron_variant PACA-CA 5 150447395 150447395 single base substitution C T upstream_gene_variant PACA-CA 5 150451223 150451223 single base substitution G C intron_variant PACA-CA 5 150454630 150454630 single base substitution G A downstream_gene_variant PACA-CA 5 150454630 150454630 single base substitution G A intron_variant PACA-CA 5 150460588 150460588 single base substitution G C 5_prime_UTR_premature_start_codon_gain_variant PACA-CA 5 150460588 150460588 single base substitution G C intron_variant PACA-CA 5 150460588 150460588 single base substitution G C upstream_gene_variant PACA-CA 5 150461372 150461372 single base substitution G A intron_variant PACA-CA 5 150461372 150461372 single base substitution G A upstream_gene_variant PACA-CA 5 150467405 150467405 single base substitution C T intron_variant PACA-CA 5 150467405 150467405 single base substitution C T upstream_gene_variant PACA-CA 5 150476157 150476157 single base substitution A T upstream_gene_variant PACA-CA 5 150477375 150477375 single base substitution C A upstream_gene_variant PAEN-AU 5 150413893 150413893 single base substitution T G downstream_gene_variant PAEN-AU 5 150413893 150413893 single base substitution T G intron_variant PAEN-AU 5 150472371 150472371 single base substitution C G intron_variant PAEN-IT 5 150457750 150457750 single base substitution C A downstream_gene_variant PAEN-IT 5 150457750 150457750 single base substitution C A intron_variant PAEN-IT 5 150465566 150465566 single base substitution C A intron_variant PAEN-IT 5 150465566 150465566 single base substitution C A upstream_gene_variant PAEN-IT 5 150468822 150468822 single base substitution G C intron_variant PAEN-IT 5 150468822 150468822 single base substitution G C upstream_gene_variant PBCA-DE 5 150412776 150412776 single base substitution G A downstream_gene_variant PBCA-DE 5 150412776 150412776 single base substitution G A intron_variant PBCA-DE 5 150425240 150425240 single base substitution G T downstream_gene_variant PBCA-DE 5 150425240 150425240 single base substitution G T intron_variant PBCA-DE 5 150444590 150444590 single base substitution C T intron_variant PBCA-DE 5 150444590 150444590 single base substitution C T missense_variant A23T 67G>A PBCA-DE 5 150444590 150444590 single base substitution C T upstream_gene_variant PBCA-DE 5 150451092 150451092 single base substitution A C intron_variant PBCA-DE 5 150454028 150454028 single base substitution G A downstream_gene_variant PBCA-DE 5 150454028 150454028 single base substitution G A intron_variant PBCA-DE 5 150470904 150470904 single base substitution G A intron_variant PBCA-DE 5 150470904 150470904 single base substitution G A upstream_gene_variant PRAD-CA 5 150432566 150432566 single base substitution C T intron_variant PRAD-CA 5 150432566 150432566 single base substitution C T upstream_gene_variant PRAD-CA 5 150437094 150437094 single base substitution G A downstream_gene_variant PRAD-CA 5 150437094 150437094 single base substitution G A intron_variant PRAD-CA 5 150439340 150439340 single base substitution C G downstream_gene_variant PRAD-CA 5 150439340 150439340 single base substitution C G intron_variant PRAD-CA 5 150439387 150439387 single base substitution A T downstream_gene_variant PRAD-CA 5 150439387 150439387 single base substitution A T intron_variant PRAD-CA 5 150439427 150439427 single base substitution T C downstream_gene_variant PRAD-CA 5 150439427 150439427 single base substitution T C intron_variant PRAD-CA 5 150443795 150443795 single base substitution G A intron_variant PRAD-CA 5 150443795 150443795 single base substitution G A upstream_gene_variant PRAD-CA 5 150476247 150476247 single base substitution C A upstream_gene_variant PRAD-UK 5 150404755 150404755 single base substitution G C downstream_gene_variant PRAD-UK 5 150414771 150414771 single base substitution G A intron_variant PRAD-UK 5 150434026 150434026 single base substitution G C intron_variant PRAD-UK 5 150434026 150434026 single base substitution G C upstream_gene_variant PRAD-UK 5 150442302 150442302 deletion of <=200bp C - intron_variant PRAD-UK 5 150445030 150445030 single base substitution C A intron_variant PRAD-UK 5 150445030 150445030 single base substitution C A upstream_gene_variant PRAD-UK 5 150463029 150463029 single base substitution C T intron_variant PRAD-UK 5 150463029 150463029 single base substitution C T upstream_gene_variant PRAD-UK 5 150466096 150466096 single base substitution G C intron_variant PRAD-UK 5 150476137 150476137 single base substitution C T upstream_gene_variant PRAD-US 5 150415234 150415234 single base substitution C T exon_variant PRAD-US 5 150415234 150415234 single base substitution C T intron_variant PRAD-US 5 150415234 150415234 single base substitution C T missense_variant R424H 1271G>A PRAD-US 5 150415234 150415234 single base substitution C T missense_variant R477H 1430G>A PRAD-US 5 150415234 150415234 single base substitution C T missense_variant R90H 269G>A PRAD-US 5 150415234 150415234 single base substitution C T upstream_gene_variant PRAD-US 5 150422163 150422163 single base substitution G A downstream_gene_variant PRAD-US 5 150422163 150422163 single base substitution G A exon_variant PRAD-US 5 150422163 150422163 single base substitution G A intron_variant PRAD-US 5 150422163 150422163 single base substitution G A stop_gained Q305* 913C>T PRAD-US 5 150422163 150422163 single base substitution G A stop_gained Q358* 1072C>T PRAD-US 5 150422163 150422163 single base substitution G A upstream_gene_variant PRAD-US 5 150444612 150444612 single base substitution G A intron_variant PRAD-US 5 150444612 150444612 single base substitution G A synonymous_variant S15S 45C>T PRAD-US 5 150444612 150444612 single base substitution G A upstream_gene_variant RECA-EU 5 150407644 150407644 single base substitution C A downstream_gene_variant RECA-EU 5 150409934 150409934 single base substitution G T 3_prime_UTR_variant RECA-EU 5 150409934 150409934 single base substitution G T downstream_gene_variant RECA-EU 5 150409934 150409934 single base substitution G T intron_variant RECA-EU 5 150411317 150411317 single base substitution C T downstream_gene_variant RECA-EU 5 150411317 150411317 single base substitution C T intron_variant RECA-EU 5 150412539 150412539 single base substitution T C downstream_gene_variant RECA-EU 5 150412539 150412539 single base substitution T C intron_variant RECA-EU 5 150414640 150414640 single base substitution A G intron_variant RECA-EU 5 150422054 150422054 single base substitution T G downstream_gene_variant RECA-EU 5 150422054 150422054 single base substitution T G intron_variant RECA-EU 5 150422054 150422054 single base substitution T G upstream_gene_variant RECA-EU 5 150422063 150422063 single base substitution G T downstream_gene_variant RECA-EU 5 150422063 150422063 single base substitution G T intron_variant RECA-EU 5 150422063 150422063 single base substitution G T upstream_gene_variant RECA-EU 5 150424081 150424081 single base substitution T C downstream_gene_variant RECA-EU 5 150424081 150424081 single base substitution T C intron_variant RECA-EU 5 150430040 150430040 single base substitution G A intron_variant RECA-EU 5 150430040 150430040 single base substitution G A upstream_gene_variant RECA-EU 5 150432668 150432668 single base substitution T C intron_variant RECA-EU 5 150432668 150432668 single base substitution T C upstream_gene_variant RECA-EU 5 150439631 150439631 single base substitution A G downstream_gene_variant RECA-EU 5 150439631 150439631 single base substitution A G intron_variant RECA-EU 5 150440625 150440625 single base substitution G T intron_variant RECA-EU 5 150443649 150443649 single base substitution C T intron_variant RECA-EU 5 150443649 150443649 single base substitution C T upstream_gene_variant RECA-EU 5 150449080 150449080 single base substitution T C intron_variant RECA-EU 5 150449080 150449080 single base substitution T C upstream_gene_variant RECA-EU 5 150449892 150449892 single base substitution A G intron_variant RECA-EU 5 150450337 150450337 single base substitution G A intron_variant RECA-EU 5 150467115 150467115 single base substitution G A intron_variant RECA-EU 5 150467115 150467115 single base substitution G A upstream_gene_variant RECA-EU 5 150475829 150475829 single base substitution C T upstream_gene_variant SKCA-BR 5 150405767 150405767 single base substitution G A downstream_gene_variant SKCA-BR 5 150406425 150406425 single base substitution G A downstream_gene_variant SKCA-BR 5 150406580 150406580 single base substitution T C downstream_gene_variant SKCA-BR 5 150407485 150407485 single base substitution A C downstream_gene_variant SKCA-BR 5 150407939 150407939 single base substitution C T downstream_gene_variant SKCA-BR 5 150413233 150413233 single base substitution T G downstream_gene_variant SKCA-BR 5 150413233 150413233 single base substitution T G exon_variant SKCA-BR 5 150413233 150413233 single base substitution T G intron_variant SKCA-BR 5 150413233 150413233 single base substitution T G missense_variant Y519S 1556A>C SKCA-BR 5 150413233 150413233 single base substitution T G missense_variant Y572S 1715A>C SKCA-BR 5 150413908 150413908 single base substitution A G downstream_gene_variant SKCA-BR 5 150413908 150413908 single base substitution A G intron_variant SKCA-BR 5 150413984 150413984 single base substitution T G downstream_gene_variant SKCA-BR 5 150413984 150413984 single base substitution T G intron_variant SKCA-BR 5 150414853 150414853 single base substitution C G intron_variant SKCA-BR 5 150418556 150418556 single base substitution T G downstream_gene_variant SKCA-BR 5 150418556 150418556 single base substitution T G intron_variant SKCA-BR 5 150418556 150418556 single base substitution T G upstream_gene_variant SKCA-BR 5 150418793 150418793 single base substitution G A downstream_gene_variant SKCA-BR 5 150418793 150418793 single base substitution G A intron_variant SKCA-BR 5 150418793 150418793 single base substitution G A splice_region_variant SKCA-BR 5 150418793 150418793 single base substitution G A upstream_gene_variant SKCA-BR 5 150421560 150421560 single base substitution G C downstream_gene_variant SKCA-BR 5 150421560 150421560 single base substitution G C intron_variant SKCA-BR 5 150421560 150421560 single base substitution G C upstream_gene_variant SKCA-BR 5 150430424 150430424 single base substitution A G intron_variant SKCA-BR 5 150430424 150430424 single base substitution A G upstream_gene_variant SKCA-BR 5 150431772 150431772 single base substitution A G exon_variant SKCA-BR 5 150431772 150431772 single base substitution A G synonymous_variant L173L 517T>C SKCA-BR 5 150431772 150431772 single base substitution A G synonymous_variant L226L 676T>C SKCA-BR 5 150431772 150431772 single base substitution A G upstream_gene_variant SKCA-BR 5 150433407 150433407 single base substitution A G intron_variant SKCA-BR 5 150433407 150433407 single base substitution A G upstream_gene_variant SKCA-BR 5 150433754 150433754 single base substitution G A intron_variant SKCA-BR 5 150433754 150433754 single base substitution G A upstream_gene_variant SKCA-BR 5 150434421 150434421 single base substitution C T intron_variant SKCA-BR 5 150434421 150434421 single base substitution C T upstream_gene_variant SKCA-BR 5 150434422 150434422 single base substitution A G intron_variant SKCA-BR 5 150434422 150434422 single base substitution A G upstream_gene_variant SKCA-BR 5 150435645 150435645 single base substitution T C downstream_gene_variant SKCA-BR 5 150435645 150435645 single base substitution T C intron_variant SKCA-BR 5 150439340 150439340 single base substitution C G downstream_gene_variant SKCA-BR 5 150439340 150439340 single base substitution C G intron_variant SKCA-BR 5 150439383 150439391 deletion of <=200bp AGAGAGAGT - downstream_gene_variant SKCA-BR 5 150439383 150439391 deletion of <=200bp AGAGAGAGT - intron_variant SKCA-BR 5 150439385 150439385 single base substitution A T downstream_gene_variant SKCA-BR 5 150439385 150439385 single base substitution A T intron_variant SKCA-BR 5 150439425 150439437 deletion of <=200bp TGTGCGCGCGCGC - downstream_gene_variant SKCA-BR 5 150439425 150439437 deletion of <=200bp TGTGCGCGCGCGC - intron_variant SKCA-BR 5 150440721 150440721 single base substitution A C intron_variant SKCA-BR 5 150442522 150442522 single base substitution G A intron_variant SKCA-BR 5 150446272 150446272 single base substitution G A intron_variant SKCA-BR 5 150446272 150446272 single base substitution G A upstream_gene_variant SKCA-BR 5 150450153 150450153 single base substitution A T intron_variant SKCA-BR 5 150456850 150456850 single base substitution G A downstream_gene_variant SKCA-BR 5 150456850 150456850 single base substitution G A intron_variant SKCA-BR 5 150460357 150460357 single base substitution T C intron_variant SKCA-BR 5 150460704 150460704 single base substitution T G 5_prime_UTR_variant SKCA-BR 5 150460704 150460704 single base substitution T G intron_variant SKCA-BR 5 150460704 150460704 single base substitution T G upstream_gene_variant SKCA-BR 5 150463460 150463460 single base substitution C T intron_variant SKCA-BR 5 150463460 150463460 single base substitution C T upstream_gene_variant SKCA-BR 5 150464527 150464527 single base substitution G A intron_variant SKCA-BR 5 150464527 150464527 single base substitution G A upstream_gene_variant SKCA-BR 5 150470403 150470403 single base substitution A G intron_variant SKCA-BR 5 150470403 150470403 single base substitution A G upstream_gene_variant SKCA-BR 5 150471700 150471700 single base substitution T C intron_variant SKCA-BR 5 150471700 150471700 single base substitution T C upstream_gene_variant SKCA-BR 5 150471727 150471727 insertion of <=200bp - GT intron_variant SKCA-BR 5 150471727 150471727 insertion of <=200bp - GT upstream_gene_variant SKCA-BR 5 150471728 150471728 single base substitution G T intron_variant SKCA-BR 5 150471728 150471728 single base substitution G T upstream_gene_variant SKCA-BR 5 150472138 150472138 insertion of <=200bp - CA intron_variant SKCA-BR 5 150472138 150472138 insertion of <=200bp - CA upstream_gene_variant SKCA-BR 5 150472349 150472349 single base substitution T G intron_variant SKCA-BR 5 150472927 150472927 insertion of <=200bp - CCTTTTTTTTTTTT intron_variant SKCA-BR 5 150473533 150473533 single base substitution C T upstream_gene_variant SKCA-BR 5 150473631 150473631 single base substitution G A upstream_gene_variant SKCA-BR 5 150474807 150474807 insertion of <=200bp - AAC upstream_gene_variant SKCM-US 5 150404937 150404937 single base substitution G A downstream_gene_variant SKCM-US 5 150404944 150404944 single base substitution G A downstream_gene_variant SKCM-US 5 150407532 150407532 single base substitution G A downstream_gene_variant SKCM-US 5 150411874 150411874 single base substitution G A 3_prime_UTR_variant SKCM-US 5 150411874 150411874 single base substitution G A downstream_gene_variant SKCM-US 5 150411874 150411874 single base substitution G A exon_variant SKCM-US 5 150411874 150411874 single base substitution G A intron_variant SKCM-US 5 150411874 150411874 single base substitution G A missense_variant P553L 1658C>T SKCM-US 5 150411874 150411874 single base substitution G A missense_variant P564L 1691C>T SKCM-US 5 150411874 150411874 single base substitution G A missense_variant P617L 1850C>T SKCM-US 5 150411892 150411892 single base substitution C T 3_prime_UTR_variant SKCM-US 5 150411892 150411892 single base substitution C T downstream_gene_variant SKCM-US 5 150411892 150411892 single base substitution C T exon_variant SKCM-US 5 150411892 150411892 single base substitution C T intron_variant SKCM-US 5 150411892 150411892 single base substitution C T missense_variant S547N 1640G>A SKCM-US 5 150411892 150411892 single base substitution C T missense_variant S558N 1673G>A SKCM-US 5 150411892 150411892 single base substitution C T missense_variant S611N 1832G>A SKCM-US 5 150411944 150411944 single base substitution G A downstream_gene_variant SKCM-US 5 150411944 150411944 single base substitution G A exon_variant SKCM-US 5 150411944 150411944 single base substitution G A intron_variant SKCM-US 5 150411944 150411944 single base substitution G A missense_variant P530S 1588C>T SKCM-US 5 150411944 150411944 single base substitution G A missense_variant P541S 1621C>T SKCM-US 5 150411944 150411944 single base substitution G A missense_variant P594S 1780C>T SKCM-US 5 150411944 150411944 single base substitution G A splice_region_variant SKCM-US 5 150413312 150413312 single base substitution C G downstream_gene_variant SKCM-US 5 150413312 150413312 single base substitution C G exon_variant SKCM-US 5 150413312 150413312 single base substitution C G intron_variant SKCM-US 5 150413312 150413312 single base substitution C G missense_variant G493R 1477G>C SKCM-US 5 150413312 150413312 single base substitution C G missense_variant G546R 1636G>C SKCM-US 5 150436378 150436378 single base substitution G A downstream_gene_variant SKCM-US 5 150436378 150436378 single base substitution G A exon_variant SKCM-US 5 150436378 150436378 single base substitution G A synonymous_variant N139N 417C>T SKCM-US 5 150436378 150436378 single base substitution G A synonymous_variant N192N 576C>T SKCM-US 5 150436501 150436501 single base substitution G A downstream_gene_variant SKCM-US 5 150436501 150436501 single base substitution G A exon_variant SKCM-US 5 150436501 150436501 single base substitution G A synonymous_variant P151P 453C>T SKCM-US 5 150436501 150436501 single base substitution G A synonymous_variant P98P 294C>T SKCM-US 5 150439957 150439957 single base substitution C A splice_acceptor_variant SKCM-US 5 150443209 150443209 single base substitution G A exon_variant SKCM-US 5 150443209 150443209 single base substitution G A missense_variant S26F 77C>T SKCM-US 5 150443209 150443209 single base substitution G A missense_variant S79F 236C>T STAD-US 5 150407589 150407589 single base substitution A G downstream_gene_variant STAD-US 5 150410293 150410293 single base substitution T C 3_prime_UTR_variant STAD-US 5 150410293 150410293 single base substitution T C downstream_gene_variant STAD-US 5 150410293 150410293 single base substitution T C exon_variant STAD-US 5 150410293 150410293 single base substitution T C intron_variant STAD-US 5 150410293 150410293 single base substitution T C missense_variant D567G 1700A>G STAD-US 5 150410293 150410293 single base substitution T C missense_variant D578G 1733A>G STAD-US 5 150410293 150410293 single base substitution T C missense_variant D631G 1892A>G STAD-US 5 150410293 150410293 single base substitution T C missense_variant T535A 1603A>G STAD-US 5 150411891 150411891 single base substitution G T 3_prime_UTR_variant STAD-US 5 150411891 150411891 single base substitution G T downstream_gene_variant STAD-US 5 150411891 150411891 single base substitution G T exon_variant STAD-US 5 150411891 150411891 single base substitution G T intron_variant STAD-US 5 150411891 150411891 single base substitution G T missense_variant S547R 1641C>A STAD-US 5 150411891 150411891 single base substitution G T missense_variant S558R 1674C>A STAD-US 5 150411891 150411891 single base substitution G T missense_variant S611R 1833C>A STAD-US 5 150418747 150418747 single base substitution G A downstream_gene_variant STAD-US 5 150418747 150418747 single base substitution G A exon_variant STAD-US 5 150418747 150418747 single base substitution G A intron_variant STAD-US 5 150418747 150418747 single base substitution G A missense_variant R339C 1015C>T STAD-US 5 150418747 150418747 single base substitution G A missense_variant R392C 1174C>T STAD-US 5 150418747 150418747 single base substitution G A missense_variant R5C 13C>T STAD-US 5 150418747 150418747 single base substitution G A upstream_gene_variant STAD-US 5 150422141 150422141 single base substitution C T downstream_gene_variant STAD-US 5 150422141 150422141 single base substitution C T exon_variant STAD-US 5 150422141 150422141 single base substitution C T intron_variant STAD-US 5 150422141 150422141 single base substitution C T missense_variant R312H 935G>A STAD-US 5 150422141 150422141 single base substitution C T missense_variant R365H 1094G>A STAD-US 5 150422141 150422141 single base substitution C T upstream_gene_variant STAD-US 5 150422226 150422226 single base substitution C A downstream_gene_variant STAD-US 5 150422226 150422226 single base substitution C A exon_variant STAD-US 5 150422226 150422226 single base substitution C A intron_variant STAD-US 5 150422226 150422226 single base substitution C A stop_gained E284* 850G>T STAD-US 5 150422226 150422226 single base substitution C A stop_gained E337* 1009G>T STAD-US 5 150422226 150422226 single base substitution C A upstream_gene_variant STAD-US 5 150436492 150436492 single base substitution G A downstream_gene_variant STAD-US 5 150436492 150436492 single base substitution G A exon_variant STAD-US 5 150436492 150436492 single base substitution G A synonymous_variant D101D 303C>T STAD-US 5 150436492 150436492 single base substitution G A synonymous_variant D154D 462C>T STAD-US 5 150436498 150436498 single base substitution A G downstream_gene_variant STAD-US 5 150436498 150436498 single base substitution A G exon_variant STAD-US 5 150436498 150436498 single base substitution A G synonymous_variant R152R 456T>C STAD-US 5 150436498 150436498 single base substitution A G synonymous_variant R99R 297T>C THCA-SA 5 150413219 150413219 single base substitution T G downstream_gene_variant THCA-SA 5 150413219 150413219 single base substitution T G exon_variant THCA-SA 5 150413219 150413219 single base substitution T G intron_variant THCA-SA 5 150413219 150413219 single base substitution T G missense_variant M524L 1570A>C THCA-SA 5 150413219 150413219 single base substitution T G missense_variant M577L 1729A>C THCA-SA 5 150436517 150436517 single base substitution G A downstream_gene_variant THCA-SA 5 150436517 150436517 single base substitution G A missense_variant A146V 437C>T THCA-SA 5 150436517 150436517 single base substitution G A missense_variant A93V 278C>T THCA-SA 5 150436517 150436517 single base substitution G A splice_region_variant THCA-US 5 150411907 150411907 single base substitution C T 3_prime_UTR_variant THCA-US 5 150411907 150411907 single base substitution C T downstream_gene_variant THCA-US 5 150411907 150411907 single base substitution C T exon_variant THCA-US 5 150411907 150411907 single base substitution C T intron_variant THCA-US 5 150411907 150411907 single base substitution C T missense_variant R542Q 1625G>A THCA-US 5 150411907 150411907 single base substitution C T missense_variant R553Q 1658G>A THCA-US 5 150411907 150411907 single base substitution C T missense_variant R606Q 1817G>A UCEC-US 5 150407084 150407084 single base substitution T G downstream_gene_variant UCEC-US 5 150407669 150407669 single base substitution C T downstream_gene_variant UCEC-US 5 150411857 150411857 single base substitution T C 3_prime_UTR_variant UCEC-US 5 150411857 150411857 single base substitution T C downstream_gene_variant UCEC-US 5 150411857 150411857 single base substitution T C exon_variant UCEC-US 5 150411857 150411857 single base substitution T C intron_variant UCEC-US 5 150411857 150411857 single base substitution T C missense_variant T559A 1675A>G UCEC-US 5 150411857 150411857 single base substitution T C missense_variant T570A 1708A>G UCEC-US 5 150411857 150411857 single base substitution T C missense_variant T623A 1867A>G UCEC-US 5 150416376 150416376 single base substitution G A exon_variant UCEC-US 5 150416376 150416376 single base substitution G A intron_variant UCEC-US 5 150416376 150416376 single base substitution G A missense_variant T404M 1211C>T UCEC-US 5 150416376 150416376 single base substitution G A missense_variant T457M 1370C>T UCEC-US 5 150416376 150416376 single base substitution G A missense_variant T70M 209C>T UCEC-US 5 150416376 150416376 single base substitution G A upstream_gene_variant UCEC-US 5 150418783 150418783 single base substitution C T downstream_gene_variant UCEC-US 5 150418783 150418783 single base substitution C T exon_variant UCEC-US 5 150418783 150418783 single base substitution C T intron_variant UCEC-US 5 150418783 150418783 single base substitution C T missense_variant D327N 979G>A UCEC-US 5 150418783 150418783 single base substitution C T missense_variant D380N 1138G>A UCEC-US 5 150418783 150418783 single base substitution C T upstream_gene_variant UCEC-US 5 150422142 150422142 single base substitution G A downstream_gene_variant UCEC-US 5 150422142 150422142 single base substitution G A exon_variant UCEC-US 5 150422142 150422142 single base substitution G A intron_variant UCEC-US 5 150422142 150422142 single base substitution G A missense_variant R312C 934C>T UCEC-US 5 150422142 150422142 single base substitution G A missense_variant R365C 1093C>T UCEC-US 5 150422142 150422142 single base substitution G A upstream_gene_variant UCEC-US 5 150425460 150425460 single base substitution C T exon_variant UCEC-US 5 150425460 150425460 single base substitution C T intron_variant UCEC-US 5 150425460 150425460 single base substitution C T missense_variant E247K 739G>A UCEC-US 5 150425460 150425460 single base substitution C T missense_variant E300K 898G>A UCEC-US 5 150425499 150425499 single base substitution C T exon_variant UCEC-US 5 150425499 150425499 single base substitution C T missense_variant A234T 700G>A UCEC-US 5 150425499 150425499 single base substitution C T missense_variant A287T 859G>A UCEC-US 5 150443195 150443195 single base substitution C T exon_variant UCEC-US 5 150443195 150443195 single base substitution C T missense_variant D31N 91G>A UCEC-US 5 150443195 150443195 single base substitution C T missense_variant D84N 250G>A UCEC-US 5 150444543 150444543 single base substitution T G intron_variant UCEC-US 5 150444543 150444543 single base substitution T G missense_variant K38N 114A>C UCEC-US 5 150444543 150444543 single base substitution T G upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-EE-A2ML-06 COSM3612626 c.453C>T p.P151P Substitution - coding silent 5:151056940-151056940 - TCGA-32-2638-01 COSM3409145 c.951T>C p.D317D Substitution - coding silent 4:163133236-163133236 - TCGA-IR-A3LH-01 COSM4833048 c.416C>T p.S139L Substitution - Missense 4:163164341-163164341 - TCGA-BH-A0HF-01 COSM3827441 c.915G>A p.M305I Substitution - Missense 5:151045882-151045882 - CSCC-19-T COSM4557413 c.727G>A p.E243K Substitution - Missense 5:151049943-151049943 - TCGA-BP-5185-01 COSM481021 c.1463C>A p.S488Y Substitution - Missense 4:163128919-163128919 - RMS85_ COSM4988937 c.800C>T p.P267L Substitution - Missense 5:151049870-151049870 - TCGA-09-2056-01 COSM71777 c.647C>G p.S216C Substitution - Missense 4:163145852-163145852 - WSU-HN30 COSM4600514 c.1322C>T p.P441L Substitution - Missense 4:163129060-163129060 - TCGA-BS-A0UV-01 COSM1064488 c.1138G>A p.D380N Substitution - Missense 5:151039222-151039222 - LUAD-D02185 COSM338756 c.1282G>T p.V428L Substitution - Missense 4:163129100-163129100 - UM-SCC-2 COSM4590251 c.1729A>C p.M577L Substitution - Missense 5:151033658-151033658 - 2290929 COSM4439971 c.1471G>T p.G491* Substitution - Nonsense 4:163128911-163128911 - TCGA-AX-A0IW-01 COSM1052834 c.576G>A p.L192L Substitution - coding silent 4:163148399-163148399 - Pat_02_B COSM5867895 c.1750C>T p.P584S Substitution - Missense 5:151033637-151033637 - sysucc-1370T COSM1052831 c.1106G>A p.R369H Substitution - Missense 4:163129276-163129276 - TCGA-60-2698-01 COSM737204 c.1334G>T p.G445V Substitution - Missense 5:151036851-151036851 - pfg068T COSM4747982 c.1721delC p.P574fs*41 Deletion - Frameshift 5:151033666-151033666 - WA16 COSM241964 c.721C>T p.R241W Substitution - Missense 5:151052166-151052166 - Pat_05_A COSM5865995 c.1243A>G p.N415D Substitution - Missense 4:163129139-163129139 - TCGA-BQ-5882-01 COSM3993531 c.1413C>T p.P471P Substitution - coding silent 4:163128969-163128969 - SNUH_G22_S1 COSM3683798 c.1740G>C p.E580D Substitution - Missense 5:151033647-151033647 - RK126_C01 COSM1634069 c.1089T>C p.F363F Substitution - coding silent 5:151042585-151042585 - TCGA-BG-A0M4-01 COSM1052835 c.396G>A p.S132S Substitution - coding silent 4:163164361-163164361 - TCGA-HC-A6AP-01 COSM3783878 c.1072C>T p.Q358* Substitution - Nonsense 5:151042602-151042602 - TCGA-10-0930-01 COSM75548 c.1119C>G p.F373L Substitution - Missense 4:163129263-163129263 - B79 COSM1753615 c.807A>G p.I269M Substitution - Missense 4:163140294-163140294 - T2664 COSM4705427 c.70G>A p.G24R Substitution - Missense 4:163166658-163166658 - TCGA-AX-A0J1-01 COSM1064491 c.859G>A p.A287T Substitution - Missense 5:151045938-151045938 - PD4594a COSM162789 c.994C>A p.Q332K Substitution - Missense 4:163133193-163133193 - TCGA-04-1356-01 COSM80664 c.306C>G p.A102A Substitution - coding silent 5:151062178-151062178 - TCGA-DK-A2I1-01 COSM1309861 c.1234C>G p.Q412E Substitution - Missense 4:163129148-163129148 - SNU-C4 COSM4653784 c.131T>C p.L44P Substitution - Missense 4:163166597-163166597 - TCGA-D8-A27V-01 COSM1064490 c.898G>A p.E300K Substitution - Missense 5:151045899-151045899 - HCC005T COSM5808937 c.1269G>T p.L423L Substitution - coding silent 5:151036916-151036916 - 447 COSM4435137 c.996A>G p.Q332Q Substitution - coding silent 4:163133191-163133191 - TCGA-EE-A3AC-06 COSM3612624 c.1636G>C p.G546R Substitution - Missense 5:151033751-151033751 - TCGA-BR-4366-01 COSM3852846 c.1009G>T p.E337* Substitution - Nonsense 5:151042665-151042665 - SNU-175 COSM3244587 c.431C>T p.A144V Substitution - Missense 5:151060322-151060322 - LUAD-S01409 COSM346795 c.731A>C p.N244T Substitution - Missense 5:151049939-151049939 - TCGA-BS-A0UA-01 COSM1052835 c.396G>A p.S132S Substitution - coding silent 4:163164361-163164361 - TCGA-D1-A102-01 COSM1064487 c.1370C>T p.T457M Substitution - Missense 5:151036815-151036815 - TCGA-AZ-4615-01 COSM4747982 c.1721delC p.P574fs*41 Deletion - Frameshift 5:151033666-151033666 - ESO-721 COSM1268222 c.710C>T p.A237V Substitution - Missense 5:151052177-151052177 - CSCC-44-T COSM4563476 c.975G>T p.Q325H Substitution - Missense 4:163133212-163133212 - Au9 COSM235501 c.1419C>T p.F473F Substitution - coding silent 5:151035684-151035684 - CT-TC COSM4989623 c.1161G>T p.E387D Substitution - Missense 5:151039199-151039199 - T3498 COSM4734936 c.1543_1545delGAG p.E515delE Deletion - In frame 5:151035044-151035046 - HCC165T COSM3661619 c.1081C>T p.R361C Substitution - Missense 5:151042593-151042593 - TCGA-BH-A0HP-01 COSM449123 c.391G>A p.E131K Substitution - Missense 5:151060362-151060362 - TCGA-IR-A3LA-01 COSM4845536 c.580G>A p.E194K Substitution - Missense 4:163148395-163148395 - CHC2052T COSM4790085 c.231G>T p.G77G Substitution - coding silent 4:163166497-163166497 - HCC107 COSM1618556 c.522A>G p.K174K Substitution - coding silent 4:163164235-163164235 - NOKSI COSM4591217 c.192G>C p.E64D Substitution - Missense 4:163166536-163166536 - PTC-46C COSM3783793 c.1410A>C p.P470P Substitution - coding silent 4:163128972-163128972 - TCGA-39-5031-01 COSM733243 c.1234C>T p.Q412* Substitution - Nonsense 4:163129148-163129148 - CRC-20T COSM5482459 c.554T>G p.V185G Substitution - Missense 4:163148421-163148421 - MedB-1 COSM5622018 c.1170G>T p.E390D Substitution - Missense 5:151039190-151039190 - Gp5D COSM3244589 c.326A>G p.K109R Substitution - Missense 5:151062158-151062158 - STC263 COSM5060216 c.1053A>G p.V351V Substitution - coding silent 4:163129329-163129329 - CHEWS019 COSM4584890 c.1276C>T p.L426F Substitution - Missense 4:163129106-163129106 - C086 COSM5535194 c.1228C>T p.P410S Substitution - Missense 4:163129154-163129154 - TCGA-B5-A0K9-01 COSM1064490 c.898G>A p.E300K Substitution - Missense 5:151045899-151045899 - LIM2551 COSM4644648 c.1651G>A p.A551T Substitution - Missense 5:151033736-151033736 - YUSEL COSM1695183 c.509C>T p.P170L Substitution - Missense 4:163164248-163164248 - TCGA-BR-6852-01 COSM3852841 c.1833C>A p.S611R Substitution - Missense 5:151032330-151032330 - UM-SCC-11B COSM4590251 c.1729A>C p.M577L Substitution - Missense 5:151033658-151033658 - TCGA-BS-A0UV-01 COSM1064492 c.250G>A p.D84N Substitution - Missense 5:151063634-151063634 - ESCC_153 COSM5645751 c.17C>A p.A6D Substitution - Missense 4:163166711-163166711 - TCGA-B8-5158-01 COSM481022 c.1176T>C p.P392P Substitution - coding silent 4:163129206-163129206 - TCGA-37-4135-01 COSM733244 c.1424C>T p.P475L Substitution - Missense 4:163128958-163128958 - sysucc-715T COSM4644648 c.1651G>A p.A551T Substitution - Missense 5:151033736-151033736 - TCGA-DD-A3A9-01 COSM4920799 c.782A>G p.H261R Substitution - Missense 4:163140319-163140319 - LUAD-B00416 COSM331397 c.879G>A p.Q293Q Substitution - coding silent 4:163137250-163137250 - UD-SCC-2 COSM4590251 c.1729A>C p.M577L Substitution - Missense 5:151033658-151033658 - PDA_004 COSM4997963 c.532G>A p.G178S Substitution - Missense 5:151056861-151056861 - CHC2052T COSM4790085 c.231G>T p.G77G Substitution - coding silent 4:163166497-163166497 - CSCC-55-T COSM4473663 c.1865C>T p.P622L Substitution - Missense 5:151032298-151032298 - SC_9018 COSM5569920 c.1216A>T p.T406S Substitution - Missense 5:151039144-151039144 - 53M COSM5595459 c.1710C>T p.I570I Substitution - coding silent 5:151033677-151033677 - LAU50_2 COSM235502 c.1725C>T p.P575P Substitution - coding silent 5:151033662-151033662 - Pat_65_A COSM5867897 c.556C>T p.R186C Substitution - Missense 5:151056837-151056837 - 2492714 COSM5718925 c.349C>T p.P117S Substitution - Missense 5:151062135-151062135 - CN-AML-NR-08-Dx COSM5425849 c.325G>T p.D109Y Substitution - Missense 4:163166403-163166403 - TCGA-G9-6373-01 COSM3783793 c.1410A>C p.P470P Substitution - coding silent 4:163128972-163128972 - 66 COSM4747982 c.1721delC p.P574fs*41 Deletion - Frameshift 5:151033666-151033666 - pfg127T COSM3244591 c.23G>A p.R8Q Substitution - Missense 5:151065073-151065073 - TCGA-IK-8125-01 COSM3974798 c.1211A>G p.Q404R Substitution - Missense 4:163129171-163129171 - TCGA-AD-6895-01 COSM252880 c.1817G>A p.R606Q Substitution - Missense 5:151032346-151032346 - LAU50_1 COSM235502 c.1725C>T p.P575P Substitution - coding silent 5:151033662-151033662 - T16 COSM5344662 c.1412C>T p.P471L Substitution - Missense 4:163128970-163128970 - ESO-632 COSM1258674 c.1087G>C p.E363Q Substitution - Missense 4:163129295-163129295 - TCGA-HE-A5NK-01 COSM4908518 c.744A>G p.A248A Substitution - coding silent 4:163140357-163140357 - TCGA-FW-A3R5-06 COSM3919383 c.576C>T p.N192N Substitution - coding silent 5:151056817-151056817 - CHC909T COSM4806352 c.1362G>C p.E454D Substitution - Missense 5:151036823-151036823 - C086 COSM5540602 c.1347C>T p.L449L Substitution - coding silent 5:151036838-151036838 - NCI-H747 COSM3335141 c.22G>A p.A8T Substitution - Missense 4:163166706-163166706 - Br27P COSM40707 c.1137C>T p.T379T Substitution - coding silent 5:151039223-151039223 - 587316 COSM1229915 c.320G>A p.S107N Substitution - Missense 5:151062164-151062164 - TCGA-22-5472-01 COSM733239 c.132A>G p.L44L Substitution - coding silent 4:163166596-163166596 - TCGA-66-2759-01 COSM733245 c.1472G>A p.G491E Substitution - Missense 4:163128910-163128910 - TCGA-BP-5182-01 COSM481023 c.25G>T p.A9S Substitution - Missense 4:163166703-163166703 - TCGA-EE-A2MP-06 COSM3612622 c.1780C>T p.P594S Substitution - Missense 5:151032383-151032383 - PT44 COSM5926531 c.1711C>T p.R571C Substitution - Missense 5:151033676-151033676 - TCGA-B5-A0JY-01 COSM1064493 c.114A>C p.K38N Substitution - Missense 5:151064982-151064982 - CAL33 COSM4591217 c.192G>C p.E64D Substitution - Missense 4:163166536-163166536 - HCC2998 COSM1672045 c.1291A>G p.T431A Substitution - Missense 5:151036894-151036894 - TCGA-DA-A1IA-06 COSM3601549 c.203A>C p.Q68P Substitution - Missense 4:163166525-163166525 - BCM399T COSM4955333 c.1746G>A p.P582P Substitution - coding silent 5:151033641-151033641 - HCC165 COSM3661619 c.1081C>T p.R361C Substitution - Missense 5:151042593-151042593 - TCGA-BR-8680-01 COSM3852843 c.1174C>T p.R392C Substitution - Missense 5:151039186-151039186 - HCC168T COSM3661621 c.658G>T p.E220* Substitution - Nonsense 5:151052229-151052229 - P50 COSM328927 c.1123G>A p.E375K Substitution - Missense 5:151042551-151042551 - HCC2998 COSM1672045 c.1291A>G p.T431A Substitution - Missense 5:151036894-151036894 - 2_RESISTANT COSM1723318 c.771_772insA p.E258fs*27 Insertion - Frameshift 5:151049898-151049899 - TCGA-AZ-6598-01 COSM1428360 c.1397A>G p.Y466C Substitution - Missense 4:163128985-163128985 - CHC909T COSM4806352 c.1362G>C p.E454D Substitution - Missense 5:151036823-151036823 - B79-Tumor COSM1753615 c.807A>G p.I269M Substitution - Missense 4:163140294-163140294 - TCGA-DA-A1I5-06 COSM3601547 c.717+2T>C p.? Unknown 4:163145780-163145780 - CH-60-T2 COSM5651247 c.1439G>C p.R480P Substitution - Missense 5:151035664-151035664 - TCGA-D3-A51G-06 COSM3601545 c.1229C>A p.P410H Substitution - Missense 4:163129153-163129153 - CSCC-7-T COSM4469843 c.1622C>G p.P541R Substitution - Missense 5:151033765-151033765 - BRC47 COSM5026441 c.801G>A p.P267P Substitution - coding silent 5:151049869-151049869 - TCGA-D9-A1JW-06 COSM3601546 c.1119C>T p.F373F Substitution - coding silent 4:163129263-163129263 - ZZUFHECRKL-G072T COSM5432910 c.1307T>C p.L436P Substitution - Missense 4:163129075-163129075 - DLD1 COSM4625488 c.242G>A p.G81D Substitution - Missense 5:151063642-151063642 - LUAD-S01315 COSM345603 c.789G>T p.E263D Substitution - Missense 4:163140312-163140312 - 90226 COSM330482 c.451C>G p.P151A Substitution - Missense 5:151056942-151056942 - LIM2551 COSM4644650 c.1313C>T p.T438I Substitution - Missense 5:151036872-151036872 - 424 COSM4432652 c.86T>G p.V29G Substitution - Missense 5:151065010-151065010 - TCGA-66-2782-01 COSM733242 c.1057C>G p.Q353E Substitution - Missense 4:163129325-163129325 - CHC437T COSM4955333 c.1746G>A p.P582P Substitution - coding silent 5:151033641-151033641 - TCGA-A4-8517-01 COSM3994121 c.123G>C p.G41G Substitution - coding silent 5:151064973-151064973 - S02351 COSM3244569 c.1722T>C p.P574P Substitution - coding silent 5:151033665-151033665 - PTC_435 COSM4590251 c.1729A>C p.M577L Substitution - Missense 5:151033658-151033658 - TCGA-AP-A059-01 COSM1052832 c.986C>A p.S329Y Substitution - Missense 4:163133201-163133201 - TCGA-06-0171 COSM2150325 c.1104_1106delCCT p.L369delL Deletion - In frame 5:151042568-151042570 - TCGA-DJ-A3UR-01 COSM252880 c.1817G>A p.R606Q Substitution - Missense 5:151032346-151032346 - PD5960a COSM5778596 c.1169C>A p.P390H Substitution - Missense 4:163129213-163129213 - SCC-25 COSM4590251 c.1729A>C p.M577L Substitution - Missense 5:151033658-151033658 - CSCC-37-T COSM4471192 c.1704C>T p.S568S Substitution - coding silent 5:151033683-151033683 - H1672 COSM316043 c.986A>T p.Q329L Substitution - Missense 5:151042912-151042912 - WSU-HN12 COSM4591217 c.192G>C p.E64D Substitution - Missense 4:163166536-163166536 - sysucc-1640T COSM5765529 c.627+1G>A p.? Unknown 5:151056765-151056765 - WA16 COSM241965 c.488G>A p.R163H Substitution - Missense 5:151056905-151056905 - TCGA-EJ-A65J-01 COSM4393260 c.45C>T p.S15S Substitution - coding silent 5:151065051-151065051 - OVCAR-4 COSM1672046 c.179G>A p.R60Q Substitution - Missense 5:151063705-151063705 - CHC1753T COSM4952517 c.1107G>T p.L369L Substitution - coding silent 5:151042567-151042567 - TCGA-FR-A3YN-06 COSM3612630 c.236C>T p.S79F Substitution - Missense 5:151063648-151063648 - CAL27 COSM4591217 c.192G>C p.E64D Substitution - Missense 4:163166536-163166536 - sysucc-854T COSM5765079 c.1277C>T p.A426V Substitution - Missense 5:151036908-151036908 - 381_T COSM3946135 c.1187A>G p.Y396C Substitution - Missense 4:163129195-163129195 - CHC437T COSM4955333 c.1746G>A p.P582P Substitution - coding silent 5:151033641-151033641 - LUAD-E00897 COSM364684 c.1899G>T p.E633D Substitution - Missense 5:151030725-151030725 - TCGA-EE-A3AF-06 COSM3601544 c.1463C>T p.S488F Substitution - Missense 4:163128919-163128919 - ESO-175 COSM1268221 c.1886A>C p.K629T Substitution - Missense 5:151030738-151030738 - LUAD-S01346 COSM397791 c.225G>T p.A75A Substitution - coding silent 4:163166503-163166503 - BCM399T COSM4955333 c.1746G>A p.P582P Substitution - coding silent 5:151033641-151033641 - TCGA-A6-6781-01 COSM1428361 c.1322delC p.P441fs*7 Deletion - Frameshift 4:163129060-163129060 - SNU-175 COSM3244591 c.23G>A p.R8Q Substitution - Missense 5:151065073-151065073 - TCGA-CK-5916-01 COSM1435255 c.1889delA p.N630fs*>7 Deletion - Frameshift 5:151030735-151030735 - S02360 COSM3244569 c.1722T>C p.P574P Substitution - coding silent 5:151033665-151033665 - TCGA-66-2783-01 COSM733241 c.978G>A p.R326R Substitution - coding silent 4:163133209-163133209 - TCGA-HU-A4GX-01 COSM3244575 c.1094G>A p.R365H Substitution - Missense 5:151042580-151042580 - EOPC-041_tumor_01 COSM5950428 c.482T>G p.L161R Substitution - Missense 5:151056911-151056911 - 2492713 COSM5718925 c.349C>T p.P117S Substitution - Missense 5:151062135-151062135 - TCGA-D1-A17Q-01 COSM1052830 c.1392A>G p.L464L Substitution - coding silent 4:163128990-163128990 - Pat_59_B COSM5865996 c.431C>T p.S144F Substitution - Missense 4:163164326-163164326 - TCGA-A5-A0GH-01 COSM1052831 c.1106G>A p.R369H Substitution - Missense 4:163129276-163129276 - PT33 COSM5535194 c.1228C>T p.P410S Substitution - Missense 4:163129154-163129154 - 2492712 COSM5718925 c.349C>T p.P117S Substitution - Missense 5:151062135-151062135 - UM-SCC-2 COSM4591217 c.192G>C p.E64D Substitution - Missense 4:163166536-163166536 - 587220 COSM1229914 c.1646C>T p.P549L Substitution - Missense 5:151033741-151033741 - sysucc-1213T COSM5764309 c.1894C>T p.R632C Substitution - Missense 5:151030730-151030730 - YUMUL COSM5402741 c.1835C>T p.S612F Substitution - Missense 5:151032328-151032328 - TCGA-CA-6717-01 COSM1435256 c.1766G>A p.R589H Substitution - Missense 5:151033621-151033621 - SA071 COSM213289 c.1877-2A>C p.? Unknown 5:151030749-151030749 - TCGA-EE-A181-06 COSM3612620 c.1832G>A p.S611N Substitution - Missense 5:151032331-151032331 - L14 COSM5369197 c.1587+2T>C p.? Unknown 5:151035000-151035000 - RMS88_ COSM4988937 c.800C>T p.P267L Substitution - Missense 5:151049870-151049870 - CSCC-47-T COSM4463906 c.1310C>A p.P437Q Substitution - Missense 5:151036875-151036875 - TCGA-36-2551-01 COSM1328622 c.723C>T p.F241F Substitution - coding silent 4:163140378-163140378 - T3021 COSM4705425 c.162G>A p.G54G Substitution - coding silent 4:163166566-163166566 - TCGA-BS-A0UF-01 COSM1052833 c.841G>T p.D281Y Substitution - Missense 4:163140260-163140260 - ESO-859 COSM1052835 c.396G>A p.S132S Substitution - coding silent 4:163164361-163164361 - TCGA-EJ-5531-01 COSM3783793 c.1410A>C p.P470P Substitution - coding silent 4:163128972-163128972 - 93VU147T COSM4591217 c.192G>C p.E64D Substitution - Missense 4:163166536-163166536 - 2492711 COSM5718925 c.349C>T p.P117S Substitution - Missense 5:151062135-151062135 - TCGA-BS-A0TJ-01 COSM1064489 c.1093C>T p.R365C Substitution - Missense 5:151042581-151042581 - TCGA-HU-A4H4-01 COSM3852850 c.456T>C p.R152R Substitution - coding silent 5:151056937-151056937 - CRC-02T COSM5455283 c.1212G>T p.Q404H Substitution - Missense 4:163129170-163129170 - PTC-53C COSM4158893 c.127C>T p.P43S Substitution - Missense 4:163166601-163166601 - PTC_221 COSM5960194 c.236delC p.P79fs*120 Deletion - Frameshift 4:163166492-163166492 - BD72T COSM5512086 c.1334delC p.P445fs*3 Deletion - Frameshift 4:163129048-163129048 - 01-P034 COSM4584889 c.1481A>G p.Y494C Substitution - Missense 4:163128901-163128901 - PDA_083 COSM5002604 c.484A>G p.I162V Substitution - Missense 4:163164273-163164273 - TCGA-CA-6717-01 COSM1435258 c.1438C>T p.R480C Substitution - Missense 5:151035665-151035665 - 2334192 COSM316043 c.986A>T p.Q329L Substitution - Missense 5:151042912-151042912 - TCGA-CC-A3MA-01 COSM4942815 c.891A>G p.S297S Substitution - coding silent 4:163137238-163137238 - 2290929 COSM4439970 c.1416T>C p.P472P Substitution - coding silent 4:163128966-163128966 - HCC95T COSM1619858 c.329C>G p.P110R Substitution - Missense 5:151062155-151062155 - CHC1753T COSM4952517 c.1107G>T p.L369L Substitution - coding silent 5:151042567-151042567 - 93VU147T COSM4590251 c.1729A>C p.M577L Substitution - Missense 5:151033658-151033658 - 2_RESISTANT COSM1722816 c.1218C>T p.T406T Substitution - coding silent 5:151039142-151039142 - 1 COSM4166554 c.1236G>T p.Q412H Substitution - Missense 4:163129146-163129146 - CSCC-38-T COSM4525887 c.1360G>A p.E454K Substitution - Missense 5:151036825-151036825 - TCGA-MI-A75C-01 COSM4923106 c.277G>T p.D93Y Substitution - Missense 5:151062207-151062207 - H650 COSM1194799 c.146G>T p.G49V Substitution - Missense 4:163166582-163166582 - TCGA-DK-A1AC-01 COSM1309862 c.341C>T p.S114L Substitution - Missense 4:163166387-163166387 - HCC168 COSM3661621 c.658G>T p.E220* Substitution - Nonsense 5:151052229-151052229 - TCGA-CG-5721-01 COSM3852840 c.1892A>G p.D631G Substitution - Missense 5:151030732-151030732 - 2_PRE-TREATMENT COSM1722816 c.1218C>T p.T406T Substitution - coding silent 5:151039142-151039142 - TCGA-AK-3428-01 COSM3365933 c.1101C>G p.L367L Substitution - coding silent 5:151042573-151042573 - TCGA-AP-A0LM-01 COSM1064486 c.1867A>G p.T623A Substitution - Missense 5:151032296-151032296 - CHC205T COSM3761036 c.891C>T p.G297G Substitution - coding silent 5:151045906-151045906 - SMS-CTR COSM4989623 c.1161G>T p.E387D Substitution - Missense 5:151039199-151039199 - TCGA-HU-A4GN-01 COSM3852848 c.462C>T p.D154D Substitution - coding silent 5:151056931-151056931 - PD7220a COSM5797826 c.222C>T p.V74V Substitution - coding silent 4:163166506-163166506 - SWE-4C COSM1179607 c.1233C>T p.Y411Y Substitution - coding silent 5:151039127-151039127 - 23_tFL COSM4171379 c.1018C>T p.Q340* Substitution - Nonsense 5:151042656-151042656 - TCGA-G5-6235-01 COSM1566874 c.878+2T>G p.? Unknown 4:163140221-163140221 - TCGA-D1-A103-01 COSM1052835 c.396G>A p.S132S Substitution - coding silent 4:163164361-163164361 - SWE-4C COSM1179607 c.1233C>T p.Y411Y Substitution - coding silent 5:151039127-151039127 - PT37 COSM5918836 c.362C>T p.T121I Substitution - Missense 5:151060391-151060391 - CSCC-31-T COSM235501 c.1419C>T p.F473F Substitution - coding silent 5:151035684-151035684 - TCGA-GN-A266-06 COSM3612618 c.1850C>T p.P617L Substitution - Missense 5:151032313-151032313 - 540 COSM1645064 c.872C>T p.P291L Substitution - Missense 5:151045925-151045925 - Gp5D COSM3335125 c.492G>A p.K164K Substitution - coding silent 4:163164265-163164265 - HCC107T COSM1618556 c.522A>G p.K174K Substitution - coding silent 4:163164235-163164235 - LAU165 COSM235501 c.1419C>T p.F473F Substitution - coding silent 5:151035684-151035684 - TCGA-EE-A184-06 COSM3612628 c.358-1G>T p.? Unknown 5:151060396-151060396 - TCGA-HU-8602-01 COSM4123244 c.1270T>C p.F424L Substitution - Missense 4:163129112-163129112 - HCC95 COSM1619858 c.329C>G p.P110R Substitution - Missense 5:151062155-151062155 - OV207 COSM252880 c.1817G>A p.R606Q Substitution - Missense 5:151032346-151032346 - CSCC-60-T COSM4464625 c.1343C>T p.A448V Substitution - Missense 5:151036842-151036842 - CN-AML-08-T COSM5425849 c.325G>T p.D109Y Substitution - Missense 4:163166403-163166403 - TCGA-76-4934-01 COSM3409144 c.1414C>T p.P472S Substitution - Missense 4:163128968-163128968 - TCGA-AD-6889-01 COSM1435255 c.1889delA p.N630fs*>7 Deletion - Frameshift 5:151030735-151030735 - N041T COSM236502 c.784A>C p.I262L Substitution - Missense 4:163140317-163140317 - TCGA-66-2785-01 COSM737203 c.517G>A p.E173K Substitution - Missense 5:151056876-151056876 - S02328 COSM5692141 c.780G>T p.A260A Substitution - coding silent 5:151049890-151049890 - TCGA-EI-6917-01 COSM3428305 c.952G>T p.E318* Substitution - Nonsense 4:163133235-163133235 - TCGA-AM-5820-01 COSM3761036 c.891C>T p.G297G Substitution - coding silent 5:151045906-151045906 - sysucc-1221T COSM3783793 c.1410A>C p.P470P Substitution - coding silent 4:163128972-163128972 - LUAD-NYU1051S COSM368883 c.53G>T p.G18V Substitution - Missense 4:163166675-163166675 - CLL103 COSM1292056 c.1444C>T p.R482C Substitution - Missense 5:151035659-151035659 - TCGA-QU-A6IO-01 COSM4876599 c.1430G>A p.R477H Substitution - Missense 5:151035673-151035673 - ME024T COSM226147 c.1679C>T p.P560L Substitution - Missense 5:151033708-151033708 - WSU-HN6 COSM4590251 c.1729A>C p.M577L Substitution - Missense 5:151033658-151033658 - CAL33 COSM4590251 c.1729A>C p.M577L Substitution - Missense 5:151033658-151033658 - TCGA-A4-8515-01 COSM3783793 c.1410A>C p.P470P Substitution - coding silent 4:163128972-163128972 - VLTS-1 COSM5702864 c.1134+4A>G p.? Unknown 5:151042536-151042536 - TCGA-DD-A3A0-01 COSM4934682 c.526G>C p.E176Q Substitution - Missense 4:163164231-163164231 - OSCC-GB_01210111 COSM5954835 c.501G>A p.T167T Substitution - coding silent 5:151056892-151056892 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.129094;Hs.129095 4q32.2 Hs.355141 5q32-q33.1 607714 2392271|CGAP|BC012133|C/T|non-coding||2196|Validated; 2392271|CGAP|BC014008|C/T|non-coding||2137|Validated; 1530668|dbSNP|BC012133|A/C|non-coding||2507|Validated; 1530668|dbSNP|BC014008|A/C|non-coding||2448|Validated

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G SpliceDonorSNV . c.717+2T>C 4 164066932 CM A G Synonymous p.D317D c.951T>C 4 164054388 GBM A G Synonymous p.P392P c.1176T>C 4 164050358 RCCC C A IntronicSNV . c.931-209G>T 4 164054617 NSCLC C A Missense p.A9S c.25G>T 4 164087855 RCCC C G IntronicSNV . c.930+1493G>C 4 164056858 MB C G Missense p.E363Q c.1087G>C 4 164050447 ESCA C T Missense p.E165K c.493G>A 4 164085416 CM C T Missense p.E322K c.964G>A 4 164054375 CM C T Missense p.G266S c.796G>A 4 164061457 LUAD C T Missense p.G491E c.1472G>A 4 164050062 LUSC C T Missense p.R369H c.1106G>A 4 164050428 UCEC C T Synonymous p.L192L c.576G>A 4 164069551 UCEC C T Synonymous p.R326R c.978G>A 4 164054361 LUSC C T Synonymous p.S132S c.396G>A 4 164085513 ESCA G A Missense p.H489Y c.1465C>T 4 164050069 HNSC G A Missense p.P36S c.106C>T 4 164087774 HNSC G A Missense p.P438L c.1313C>T 4 164050221 CM G A Missense p.P472S c.1414C>T 4 164050120 GBM G A Missense p.P473S c.1417C>T 4 164050117 CM G A Missense p.P475L c.1424C>T 4 164050110 LUSC G A Missense p.S488F c.1463C>T 4 164050071 CM G A Nonsense p.Q412* c.1234C>T 4 164050300 LUSC G A Synonymous p.F16F c.48C>T 4 164087832 LUAD G A Synonymous p.F373F c.1119C>T 4 164050415 CM G C Missense p.F373L c.1119C>G 4 164050415 OV G C Missense p.P480A c.1438C>G 4 164050096 GBM G C Missense p.Q353E c.1057C>G 4 164050477 LUSC G C Missense p.Q412E c.1234C>G 4 164050300 BLCA G C Missense p.S142C c.425C>G 4 164085484 LUAD G C Missense p.S216C c.647C>G 4 164067004 OV G C Nonsense p.S205* c.614C>G 4 164069513 HNSC G T Missense p.Q332K c.994C>A 4 164054345 BRCA G T Missense p.S488Y c.1463C>A 4 164050071 RCCC T C Missense p.M401V c.1201A>G 4 164050333 HNSC T C Missense p.Q404R c.1211A>G 4 164050323 LGG T C Synonymous p.L44L c.132A>G 4 164087748 LUSC T G 3-UTRSNV . c.1482+133A>C 4 164049919 ESCA T G Missense p.Q68P c.203A>C 4 164087677 CM AGG - InFrameDeletion p.L369delL c.1104_1106delCCT 5 150422129 GBM A G Synonymous p.F363F c.1089T>C 5 150422146 HC C A Nonsense p.E337* c.1009G>T 5 150422226 STAD C A SpliceAcceptorSNV . c.358-1G>T 5 150439957 CM C G Missense p.G546R c.1636G>C 5 150413312 CM - CTAAAGTTACGGTTAA IntronicInsertion . c.271+471_271+472insTTAACCGTAACTTTAG 5 150442702 CLL C T Missense p.E131K c.391G>A 5 150439923 BRCA C T Missense p.E131K c.391G>A 5 150439923 LUAD C T Missense p.E300K c.898G>A 5 150425460 UCEC C T Missense p.R477H c.1430G>A 5 150415234 PRAD C T Missense p.R606Q c.1817G>A 5 150411907 THCA C T Missense p.S611N c.1832G>A 5 150411892 CM C T Synonymous p.P267P c.801G>A 5 150429430 BRCA C T Synonymous p.T379T c.1137C>T 5 150418784 GBM CTT - InFrameDeletion p.K302delK c.904_906delAAG 5 150425452 LGG G A Missense p.A237V c.710C>T 5 150431738 ESCA G A Missense p.P149L c.446C>T 5 150436508 CM G A Missense p.P594S c.1780C>T 5 150411944 CM G A Missense p.R152C c.454C>T 5 150436500 CM G A Missense p.R365C c.1093C>T 5 150422142 UCEC G A Missense p.R482C c.1444C>T 5 150415220 CLL G A Missense p.T457M c.1370C>T 5 150416376 UCEC G A Nonsense p.Q358* c.1072C>T 5 150422163 PRAD G A Synonymous p.P151P c.453C>T 5 150436501 CM G A Synonymous p.S15S c.45C>T 5 150444612 PRAD G C Synonymous p.A102A c.306C>G 5 150441739 OV G C Synonymous p.L367L c.1101C>G 5 150422134 RCCC G T Missense p.S611R c.1833C>A 5 150411891 STAD T A Missense p.Q329L c.986A>T 5 150422473 SCLC T C IntronicSNV . c.1-15175A>G 5 150459831 HC T G Missense p.K629T c.1886A>C 5 150410299 ESCA T G SpliceAcceptorSNV . c.1877-2A>C 5 150410310 BRCA