Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change ACC 9 33056173 33056173 + Missense_Mutation SNP C C T TCGA-OR-A5LJ-01A-11D-A29I-10 TCGA-OR-A5LJ-10A-01D-A29L-10 g.chr9:33056173C>T c.1060G>A c.(1060-1062)Gaa>Aaa p.E354K BLCA 9 33047347 33047347 + Missense_Mutation SNP G G C TCGA-4Z-AA86-01A-11D-A391-08 TCGA-4Z-AA86-10A-01D-A394-08 g.chr9:33047347G>C c.1486C>G c.(1486-1488)Cag>Gag p.Q496E BLCA 9 33053286 33053286 + Missense_Mutation SNP G G C TCGA-XF-AAML-01A-11D-A42E-08 TCGA-XF-AAML-10A-01D-A42H-08 g.chr9:33053286G>C c.1125C>G c.(1123-1125)atC>atG p.I375M BLCA 9 33056197 33056197 + Missense_Mutation SNP G G A TCGA-E7-A5KF-01A-11D-A289-08 TCGA-E7-A5KF-10A-01D-A289-08 g.chr9:33056197G>A c.1036C>T c.(1036-1038)Cgt>Tgt p.R346C BLCA 9 33056883 33056883 + Missense_Mutation SNP G G C TCGA-FD-A43P-01A-31D-A23U-08 TCGA-FD-A43P-10A-01D-A23U-08 g.chr9:33056883G>C c.947C>G c.(946-948)tCt>tGt p.S316C BLCA 9 33071779 33071779 + Silent SNP G G A TCGA-YF-AA3M-01A-11D-A42E-08 TCGA-YF-AA3M-10D-01D-A42H-08 g.chr9:33071779G>A c.349C>T c.(349-351)Ctg>Ttg p.L117L BRCA 9 33057640 33057640 + Missense_Mutation SNP C C T TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr9:33057640C>T c.823G>A c.(823-825)Gat>Aat p.D275N CESC 9 33073633 33073633 + Silent SNP C C T TCGA-IR-A3LK-01A-12D-A20U-09 TCGA-IR-A3LK-10A-01D-A20U-09 g.chr9:33073633C>T c.198G>A c.(196-198)ctG>ctA p.L66L COAD 9 33048119 33048119 + Silent SNP C C T TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr9:33048119C>T c.1428G>A c.(1426-1428)ctG>ctA p.L476L COAD 9 33048132 33048132 + Missense_Mutation SNP A A G TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr9:33048132A>G c.1415T>C c.(1414-1416)gTc>gCc p.V472A COAD 9 33053232 33053232 + Silent SNP G G A TCGA-AD-6901-01A-11D-1924-10 TCGA-AD-6901-10A-01D-1924-10 g.chr9:33053232G>A c.1179C>T c.(1177-1179)acC>acT p.T393T COAD 9 33056109 33056109 + Splice_Site SNP A A C TCGA-AA-3968-01A-01W-0995-10 TCGA-AA-3968-10A-01W-0995-10 g.chr9:33056109A>C c.e9+1 COAD 9 33056219 33056219 + Silent SNP A A G TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr9:33056219A>G c.1014T>C c.(1012-1014)tcT>tcC p.S338S COAD 9 33071790 33071790 + Missense_Mutation SNP C C T TCGA-G4-6303-01A-11D-1771-10 TCGA-G4-6303-10A-01D-1771-10 g.chr9:33071790C>T c.338G>A c.(337-339)cGa>cAa p.R113Q COADREAD 9 33048119 33048119 + Silent SNP C C T TCGA-AA-3815-01A-01W-0995-10 TCGA-AA-3815-10A-01W-0995-10 g.chr9:33048119C>T c.1428G>A c.(1426-1428)ctG>ctA p.L476L COADREAD 9 33048132 33048132 + Missense_Mutation SNP A A G TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr9:33048132A>G c.1415T>C c.(1414-1416)gTc>gCc p.V472A COADREAD 9 33053232 33053232 + Silent SNP G G A TCGA-AD-6901-01A-11D-1924-10 TCGA-AD-6901-10A-01D-1924-10 g.chr9:33053232G>A c.1179C>T c.(1177-1179)acC>acT p.T393T COADREAD 9 33056109 33056109 + Splice_Site SNP A A C TCGA-AA-3968-01A-01W-0995-10 TCGA-AA-3968-10A-01W-0995-10 g.chr9:33056109A>C c.e9+1 COADREAD 9 33056219 33056219 + Silent SNP A A G TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr9:33056219A>G c.1014T>C c.(1012-1014)tcT>tcC p.S338S COADREAD 9 33071790 33071790 + Missense_Mutation SNP C C T TCGA-G4-6303-01A-11D-1771-10 TCGA-G4-6303-10A-01D-1771-10 g.chr9:33071790C>T c.338G>A c.(337-339)cGa>cAa p.R113Q DLBC 9 33071879 33071879 + Silent SNP T T C TCGA-G8-6326-01A-11D-2210-10 TCGA-G8-6326-10A-01D-2210-10 g.chr9:33071879T>C c.249A>G c.(247-249)gaA>gaG p.E83E GBMLGG 9 33073796 33073796 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:33073796C>T c.35G>A c.(34-36)cGc>cAc p.R12H HNSC 9 33056843 33056843 + Missense_Mutation SNP C C G TCGA-MT-A67F-01A-11D-A30E-08 TCGA-MT-A67F-10A-01D-A30H-08 g.chr9:33056843C>G c.987G>C c.(985-987)caG>caC p.Q329H HNSC 9 33056956 33056956 + Nonsense_Mutation SNP T T A TCGA-P3-A6T5-01A-11D-A34J-08 TCGA-P3-A6T5-10A-01D-A34M-08 g.chr9:33056956T>A c.874A>T c.(874-876)Aag>Tag p.K292* KIPAN 9 33048146 33048146 + Nonsense_Mutation SNP G G C TCGA-B1-7332-01A-11D-2136-08 TCGA-B1-7332-10A-01D-2136-08 g.chr9:33048146G>C c.1401C>G c.(1399-1401)taC>taG p.Y467* KIPAN 9 33048246 33048246 + Missense_Mutation SNP C C A TCGA-Y8-A895-01A-11D-A35Z-10 TCGA-Y8-A895-10A-01D-A35Z-10 g.chr9:33048246C>A c.1301G>T c.(1300-1302)aGc>aTc p.S434I KIPAN 9 33071759 33071759 + Missense_Mutation SNP C C G TCGA-B8-5162-01A-01D-1421-08 TCGA-B8-5162-10A-01D-1421-08 g.chr9:33071759C>G c.369G>C c.(367-369)agG>agC p.R123S KIPAN 9 33073680 33073680 + Missense_Mutation SNP T T C TCGA-CJ-4875-01A-01D-1373-10 TCGA-CJ-4875-11A-01D-1373-10 g.chr9:33073680T>C c.151A>G c.(151-153)Att>Gtt p.I51V KIPAN 9 33073796 33073796 + Missense_Mutation SNP C C T TCGA-CJ-4900-01A-01D-1462-08 TCGA-CJ-4900-11A-01D-1462-08 g.chr9:33073796C>T c.35G>A c.(34-36)cGc>cAc p.R12H KIRC 9 33071759 33071759 + Missense_Mutation SNP C C G TCGA-B8-5162-01A-01D-1421-08 TCGA-B8-5162-10A-01D-1421-08 g.chr9:33071759C>G c.369G>C c.(367-369)agG>agC p.R123S KIRC 9 33073680 33073680 + Missense_Mutation SNP T T C TCGA-CJ-4875-01A-01D-1373-10 TCGA-CJ-4875-11A-01D-1373-10 g.chr9:33073680T>C c.151A>G c.(151-153)Att>Gtt p.I51V KIRC 9 33073796 33073796 + Missense_Mutation SNP C C T TCGA-CJ-4900-01A-01D-1462-08 TCGA-CJ-4900-11A-01D-1462-08 g.chr9:33073796C>T c.35G>A c.(34-36)cGc>cAc p.R12H KIRP 9 33048146 33048146 + Nonsense_Mutation SNP G G C TCGA-B1-7332-01A-11D-2136-08 TCGA-B1-7332-10A-01D-2136-08 g.chr9:33048146G>C c.1401C>G c.(1399-1401)taC>taG p.Y467* KIRP 9 33048246 33048246 + Missense_Mutation SNP C C A TCGA-Y8-A895-01A-11D-A35Z-10 TCGA-Y8-A895-10A-01D-A35Z-10 g.chr9:33048246C>A c.1301G>T c.(1300-1302)aGc>aTc p.S434I LGG 9 33073796 33073796 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr9:33073796C>T c.35G>A c.(34-36)cGc>cAc p.R12H LUAD 9 33053211 33053211 + Silent SNP G G C TCGA-55-7911-01A-11D-2167-08 TCGA-55-7911-10A-01D-2167-08 g.chr9:33053211G>C c.1200C>G c.(1198-1200)gtC>gtG p.V400V LUAD 9 33056169 33056169 + Missense_Mutation SNP G G A TCGA-55-6968-01A-11D-1945-08 TCGA-55-6968-11A-01D-1945-08 g.chr9:33056169G>A c.1064C>T c.(1063-1065)gCa>gTa p.A355V LUAD 9 33057642 33057642 + Missense_Mutation SNP C C A TCGA-78-7155-01A-11D-2036-08 TCGA-78-7155-10A-01D-2036-08 g.chr9:33057642C>A c.821G>T c.(820-822)aGa>aTa p.R274I LUAD 9 33068842 33068842 + Missense_Mutation SNP G G A TCGA-55-6968-01A-11D-1945-08 TCGA-55-6968-11A-01D-1945-08 g.chr9:33068842G>A c.481C>T c.(481-483)Ctc>Ttc p.L161F LUAD 9 33068870 33068870 + Silent SNP G G A TCGA-44-7659-01A-11D-2063-08 TCGA-44-7659-10A-01D-2063-08 g.chr9:33068870G>A c.453C>T c.(451-453)ggC>ggT p.G151G LUAD 9 33071822 33071822 + Silent SNP G G A TCGA-38-4631-01A-01D-1753-08 TCGA-38-4631-11A-01D-1753-08 g.chr9:33071822G>A c.306C>T c.(304-306)ccC>ccT p.P102P LUAD 9 33073725 33073725 + Missense_Mutation SNP C C G TCGA-35-4123-01A-01D-1105-08 TCGA-35-4123-10A-01D-1105-08 g.chr9:33073725C>G c.106G>C c.(106-108)Gtg>Ctg p.V36L LUSC 9 33053169 33053169 + Silent SNP C C A TCGA-18-3410-01A-01D-0983-08 TCGA-18-3410-11A-01D-0983-08 g.chr9:33053169C>A c.1242G>T c.(1240-1242)gtG>gtT p.V414V OV 9 33068870 33068870 + Silent SNP G G A TCGA-29-1785-01A-01W-0633-09 TCGA-29-1785-10A-01W-0634-09 g.chr9:33068870G>A c.453C>T c.(451-453)ggC>ggT p.G151G OV 9 33076580 33076580 + Splice_Site SNP C C T TCGA-23-1110-01A-01D-0428-08 TCGA-23-1110-10A-01D-0428-08 g.chr9:33076580C>T c.e1+1 PAAD 9 33068870 33068870 + Silent SNP G G A TCGA-2J-AAB9-01A-11D-A40W-08 TCGA-2J-AAB9-10A-01D-A40W-08 g.chr9:33068870G>A c.453C>T c.(451-453)ggC>ggT p.G151G PAAD 9 33068870 33068870 + Silent SNP G G A TCGA-IB-A5SS-01A-11D-A32N-08 TCGA-IB-A5SS-10A-01D-A32N-08 g.chr9:33068870G>A c.453C>T c.(451-453)ggC>ggT p.G151G PAAD 9 33068870 33068870 + Silent SNP G G A TCGA-Q3-A5QY-01A-12D-A32N-08 TCGA-Q3-A5QY-10A-01D-A32N-08 g.chr9:33068870G>A c.453C>T c.(451-453)ggC>ggT p.G151G PCPG 9 33068870 33068870 + Silent SNP G G A TCGA-QR-A7IP-01A-11D-A35D-08 TCGA-QR-A7IP-10A-01D-A35B-08 g.chr9:33068870G>A c.453C>T c.(451-453)ggC>ggT p.G151G PRAD 9 33056918 33056918 + Silent SNP C C T TCGA-G9-6385-01A-11D-1786-08 TCGA-G9-6385-10A-01D-1786-08 g.chr9:33056918C>T c.912G>A c.(910-912)agG>agA p.R304R PRAD 9 33057683 33057683 + Silent SNP A A G TCGA-YL-A8SC-01A-11D-A377-08 TCGA-YL-A8SC-10A-01D-A37A-08 g.chr9:33057683A>G c.780T>C c.(778-780)ttT>ttC p.F260F SKCM 9 33048118 33048118 + Missense_Mutation SNP C C T TCGA-RP-A693-06A-13D-A30X-08 TCGA-RP-A693-10A-01D-A30X-08 g.chr9:33048118C>T c.1429G>A c.(1429-1431)Gag>Aag p.E477K SKCM 9 33048158 33048158 + Silent SNP G G A TCGA-FS-A1ZK-06A-11D-A197-08 TCGA-FS-A1ZK-10A-01D-A199-08 g.chr9:33048158G>A c.1389C>T c.(1387-1389)gaC>gaT p.D463D SKCM 9 33056197 33056197 + Missense_Mutation SNP G G A TCGA-D9-A1JW-06A-11D-A19A-08 TCGA-D9-A1JW-10A-01D-A19A-08 g.chr9:33056197G>A c.1036C>T c.(1036-1038)Cgt>Tgt p.R346C SKCM 9 33060542 33060542 + Missense_Mutation SNP G G T TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr9:33060542G>T c.671C>A c.(670-672)cCa>cAa p.P224Q SKCM 9 33062073 33062073 + Missense_Mutation SNP G G A TCGA-ER-A19Q-06A-11D-A197-08 TCGA-ER-A19Q-10A-01D-A199-08 g.chr9:33062073G>A c.604C>T c.(604-606)Cct>Tct p.P202S SKCM 9 33062139 33062139 + Missense_Mutation SNP G G A TCGA-DA-A1HY-06A-11D-A19A-08 TCGA-DA-A1HY-10A-01D-A19A-08 g.chr9:33062139G>A c.538C>T c.(538-540)Cct>Tct p.P180S SKCM 9 33062142 33062142 + Missense_Mutation SNP G G A TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr9:33062142G>A c.535C>T c.(535-537)Cct>Tct p.P179S SKCM 9 33073695 33073695 + Missense_Mutation SNP T T C TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr9:33073695T>C c.136A>G c.(136-138)Agt>Ggt p.S46G SKCM 9 33076601 33076601 + Silent SNP C C A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr9:33076601C>A c.6G>T c.(4-6)tcG>tcT p.S2S

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BRCA-EU 9 33036773 33036773 single base substitution G A downstream_gene_variant BRCA-EU 9 33039660 33039660 single base substitution G C downstream_gene_variant BRCA-EU 9 33039688 33039688 single base substitution A T downstream_gene_variant BRCA-EU 9 33041537 33041537 single base substitution G T downstream_gene_variant BRCA-EU 9 33041993 33041993 single base substitution A G 3_prime_UTR_variant BRCA-EU 9 33042334 33042334 single base substitution G A 3_prime_UTR_variant BRCA-EU 9 33042334 33042334 single base substitution G A downstream_gene_variant BRCA-EU 9 33042432 33042433 deletion of <=200bp CT - 3_prime_UTR_variant BRCA-EU 9 33042432 33042433 deletion of <=200bp CT - downstream_gene_variant BRCA-EU 9 33043544 33043544 single base substitution G C 3_prime_UTR_variant BRCA-EU 9 33043544 33043544 single base substitution G C downstream_gene_variant BRCA-EU 9 33044582 33044582 deletion of <=200bp A - 3_prime_UTR_variant BRCA-EU 9 33044582 33044582 deletion of <=200bp A - downstream_gene_variant BRCA-EU 9 33045001 33045001 single base substitution A T 3_prime_UTR_variant BRCA-EU 9 33045001 33045001 single base substitution A T downstream_gene_variant BRCA-EU 9 33046760 33046760 single base substitution G A 3_prime_UTR_variant BRCA-EU 9 33046760 33046760 single base substitution G A downstream_gene_variant BRCA-EU 9 33047558 33047558 single base substitution A G intron_variant BRCA-EU 9 33047573 33047573 single base substitution A G intron_variant BRCA-EU 9 33048883 33048883 single base substitution G T intron_variant BRCA-EU 9 33049050 33049050 single base substitution A C intron_variant BRCA-EU 9 33050506 33050506 single base substitution T C intron_variant BRCA-EU 9 33050723 33050723 single base substitution C T intron_variant BRCA-EU 9 33052608 33052608 single base substitution C T intron_variant BRCA-EU 9 33052875 33052875 single base substitution G A intron_variant BRCA-EU 9 33053018 33053018 single base substitution A T intron_variant BRCA-EU 9 33054596 33054596 single base substitution G C intron_variant BRCA-EU 9 33054626 33054626 single base substitution T C intron_variant BRCA-EU 9 33056061 33056061 single base substitution G C intron_variant BRCA-EU 9 33058176 33058176 single base substitution T G intron_variant BRCA-EU 9 33058177 33058177 single base substitution C T intron_variant BRCA-EU 9 33060185 33060185 single base substitution A T intron_variant BRCA-EU 9 33060667 33060667 single base substitution G A intron_variant BRCA-EU 9 33060968 33060968 single base substitution C T intron_variant BRCA-EU 9 33067497 33067497 single base substitution T C intron_variant BRCA-EU 9 33068684 33068684 single base substitution G C intron_variant BRCA-EU 9 33071212 33071212 single base substitution G T intron_variant BRCA-EU 9 33072838 33072838 single base substitution A C intron_variant BRCA-EU 9 33073270 33073270 single base substitution C T intron_variant BRCA-EU 9 33073970 33073970 single base substitution A T intron_variant BRCA-EU 9 33076894 33076894 single base substitution C T upstream_gene_variant BRCA-EU 9 33077648 33077648 single base substitution G A upstream_gene_variant BRCA-EU 9 33079786 33079786 single base substitution C T upstream_gene_variant BRCA-EU 9 33079878 33079878 single base substitution A T upstream_gene_variant BRCA-EU 9 33080631 33080631 single base substitution G A upstream_gene_variant BRCA-FR 9 33036773 33036773 single base substitution G A downstream_gene_variant BRCA-FR 9 33041266 33041266 single base substitution G A downstream_gene_variant BRCA-FR 9 33043707 33043707 single base substitution G A 3_prime_UTR_variant BRCA-FR 9 33043707 33043707 single base substitution G A downstream_gene_variant BRCA-FR 9 33050506 33050506 single base substitution T C intron_variant BRCA-FR 9 33066295 33066295 single base substitution G C intron_variant BRCA-FR 9 33072741 33072741 single base substitution C T intron_variant BRCA-US 9 33037105 33037105 single base substitution G A downstream_gene_variant BRCA-US 9 33057640 33057640 single base substitution C T missense_variant D114N 340G>A BRCA-US 9 33057640 33057640 single base substitution C T missense_variant D275N 823G>A BTCA-JP 9 33038758 33038758 single base substitution G A downstream_gene_variant BTCA-JP 9 33060534 33060534 single base substitution G A stop_gained Q227* 679C>T BTCA-JP 9 33060534 33060534 single base substitution G A stop_gained Q66* 196C>T BTCA-JP 9 33062082 33062082 single base substitution C A stop_gained E199* 595G>T BTCA-JP 9 33062082 33062082 single base substitution C A stop_gained E38* 112G>T BTCA-JP 9 33062094 33062094 single base substitution C A missense_variant D195Y 583G>T BTCA-JP 9 33062094 33062094 single base substitution C A missense_variant D34Y 100G>T BTCA-JP 9 33062131 33062131 single base substitution C T missense_variant M182I 546G>A BTCA-JP 9 33062131 33062131 single base substitution C T missense_variant M21I 63G>A BTCA-JP 9 33062208 33062208 single base substitution T A intron_variant BTCA-JP 9 33062209 33062209 single base substitution C T intron_variant BTCA-JP 9 33071909 33071909 single base substitution A C intron_variant BTCA-JP 9 33071910 33071910 single base substitution C A intron_variant BTCA-JP 9 33071911 33071911 single base substitution A C intron_variant BTCA-JP 9 33076670 33076670 single base substitution G A upstream_gene_variant CESC-US 9 33038806 33038806 single base substitution G A downstream_gene_variant CESC-US 9 33073633 33073633 single base substitution C T intron_variant CESC-US 9 33073633 33073633 single base substitution C T synonymous_variant L66L 198G>A CLLE-ES 9 33063273 33063273 single base substitution T C intron_variant CLLE-ES 9 33066145 33066145 single base substitution C T intron_variant COAD-US 9 33038827 33038827 single base substitution C T downstream_gene_variant COAD-US 9 33048132 33048132 single base substitution A G missense_variant V311A 932T>C COAD-US 9 33048132 33048132 single base substitution A G missense_variant V472A 1415T>C COAD-US 9 33053232 33053232 single base substitution G A synonymous_variant T232T 696C>T COAD-US 9 33053232 33053232 single base substitution G A synonymous_variant T393T 1179C>T COAD-US 9 33056219 33056219 single base substitution A G synonymous_variant S177S 531T>C COAD-US 9 33056219 33056219 single base substitution A G synonymous_variant S338S 1014T>C COAD-US 9 33071790 33071790 single base substitution C T intron_variant COAD-US 9 33071790 33071790 single base substitution C T missense_variant R113Q 338G>A COCA-CN 9 33047211 33047211 single base substitution A C 3_prime_UTR_variant COCA-CN 9 33047211 33047211 single base substitution A C downstream_gene_variant COCA-CN 9 33048066 33048066 single base substitution C T intron_variant COCA-CN 9 33050195 33050195 single base substitution T C intron_variant COCA-CN 9 33062007 33062007 single base substitution A G intron_variant COCA-CN 9 33062262 33062262 single base substitution G A intron_variant COCA-CN 9 33068923 33068923 single base substitution C A 5_prime_UTR_variant COCA-CN 9 33068923 33068923 single base substitution C A missense_variant D134Y 400G>T COCA-CN 9 33076676 33076676 single base substitution T G upstream_gene_variant ESAD-UK 9 33037895 33037895 single base substitution G C downstream_gene_variant ESAD-UK 9 33038564 33038564 single base substitution T G downstream_gene_variant ESAD-UK 9 33039310 33039310 single base substitution G C downstream_gene_variant ESAD-UK 9 33039799 33039799 single base substitution A T downstream_gene_variant ESAD-UK 9 33043219 33043219 single base substitution A T 3_prime_UTR_variant ESAD-UK 9 33043219 33043219 single base substitution A T downstream_gene_variant ESAD-UK 9 33044273 33044273 single base substitution G T 3_prime_UTR_variant ESAD-UK 9 33044273 33044273 single base substitution G T downstream_gene_variant ESAD-UK 9 33044311 33044311 single base substitution T C 3_prime_UTR_variant ESAD-UK 9 33044311 33044311 single base substitution T C downstream_gene_variant ESAD-UK 9 33045226 33045226 deletion of <=200bp T - 3_prime_UTR_variant ESAD-UK 9 33045226 33045226 deletion of <=200bp T - downstream_gene_variant ESAD-UK 9 33055346 33055346 single base substitution A T intron_variant ESAD-UK 9 33061251 33061251 single base substitution G T intron_variant ESAD-UK 9 33069623 33069623 single base substitution A C intron_variant ESAD-UK 9 33074451 33074451 single base substitution A C intron_variant ESAD-UK 9 33079578 33079578 single base substitution T G upstream_gene_variant ESAD-UK 9 33080912 33080912 single base substitution C A upstream_gene_variant ESCA-CN 9 33056365 33056365 single base substitution G C intron_variant KIRC-US 9 33073680 33073680 single base substitution T C intron_variant KIRC-US 9 33073680 33073680 single base substitution T C missense_variant I51V 151A>G LAML-KR 9 33052015 33052015 single base substitution C A intron_variant LAML-KR 9 33062128 33062128 single base substitution G A synonymous_variant T183T 549C>T LAML-KR 9 33062128 33062128 single base substitution G A synonymous_variant T22T 66C>T LAML-KR 9 33062197 33062197 single base substitution T C intron_variant LICA-FR 9 33037319 33037319 insertion of <=200bp - C downstream_gene_variant LICA-FR 9 33047211 33047211 insertion of <=200bp - AA 3_prime_UTR_variant LICA-FR 9 33047211 33047211 insertion of <=200bp - AA downstream_gene_variant LICA-FR 9 33052476 33052476 single base substitution C T intron_variant LICA-FR 9 33053389 33053389 single base substitution T C intron_variant LICA-FR 9 33068872 33068872 single base substitution C A 5_prime_UTR_premature_start_codon_gain_variant LICA-FR 9 33068872 33068872 single base substitution C A missense_variant G151C 451G>T LIHC-US 9 33037024 33037024 single base substitution A G downstream_gene_variant LIHC-US 9 33037026 33037026 single base substitution G A downstream_gene_variant LINC-JP 9 33038285 33038285 single base substitution G A downstream_gene_variant LINC-JP 9 33042105 33042108 deletion of <=200bp AAAG - 3_prime_UTR_variant LINC-JP 9 33042296 33042296 single base substitution A G 3_prime_UTR_variant LINC-JP 9 33042296 33042296 single base substitution A G downstream_gene_variant LINC-JP 9 33052292 33052292 single base substitution A C intron_variant LINC-JP 9 33056961 33056961 single base substitution A G missense_variant V129A 386T>C LINC-JP 9 33056961 33056961 single base substitution A G missense_variant V290A 869T>C LINC-JP 9 33069118 33069118 single base substitution T C intron_variant LINC-JP 9 33072964 33072964 single base substitution G C intron_variant LIRI-JP 9 33036903 33036903 single base substitution C T downstream_gene_variant LIRI-JP 9 33038143 33038143 single base substitution C T downstream_gene_variant LIRI-JP 9 33038926 33038926 single base substitution C T downstream_gene_variant LIRI-JP 9 33038952 33038952 single base substitution G A downstream_gene_variant LIRI-JP 9 33041111 33041111 single base substitution A G downstream_gene_variant LIRI-JP 9 33041150 33041150 single base substitution T G downstream_gene_variant LIRI-JP 9 33042017 33042017 single base substitution C T 3_prime_UTR_variant LIRI-JP 9 33046259 33046259 single base substitution G T 3_prime_UTR_variant LIRI-JP 9 33046259 33046259 single base substitution G T downstream_gene_variant LIRI-JP 9 33047789 33047789 single base substitution A T intron_variant LIRI-JP 9 33048288 33048288 single base substitution T A intron_variant LIRI-JP 9 33048539 33048539 single base substitution T C intron_variant LIRI-JP 9 33049482 33049482 single base substitution T A intron_variant LIRI-JP 9 33052322 33052322 single base substitution A C intron_variant LIRI-JP 9 33052477 33052477 insertion of <=200bp - GAT intron_variant LIRI-JP 9 33056040 33056040 single base substitution A G intron_variant LIRI-JP 9 33057156 33057156 single base substitution T C intron_variant LIRI-JP 9 33061119 33061119 single base substitution T C intron_variant LIRI-JP 9 33062570 33062570 single base substitution A G intron_variant LIRI-JP 9 33065763 33065763 single base substitution G A intron_variant LIRI-JP 9 33071544 33071544 single base substitution G A intron_variant LIRI-JP 9 33072912 33072912 single base substitution G A intron_variant LIRI-JP 9 33075002 33075002 single base substitution C T intron_variant LIRI-JP 9 33078184 33078184 single base substitution G A upstream_gene_variant LIRI-JP 9 33080229 33080229 single base substitution C T upstream_gene_variant LIRI-JP 9 33080437 33080437 single base substitution G A upstream_gene_variant LIRI-JP 9 33081519 33081519 single base substitution G T upstream_gene_variant LUSC-KR 9 33039024 33039024 single base substitution T A downstream_gene_variant LUSC-KR 9 33042562 33042562 single base substitution C A 3_prime_UTR_variant LUSC-KR 9 33042562 33042562 single base substitution C A downstream_gene_variant LUSC-KR 9 33042615 33042615 single base substitution C T 3_prime_UTR_variant LUSC-KR 9 33042615 33042615 single base substitution C T downstream_gene_variant LUSC-KR 9 33043718 33043718 single base substitution G A 3_prime_UTR_variant LUSC-KR 9 33043718 33043718 single base substitution G A downstream_gene_variant LUSC-KR 9 33045147 33045147 single base substitution A G 3_prime_UTR_variant LUSC-KR 9 33045147 33045147 single base substitution A G downstream_gene_variant LUSC-KR 9 33045161 33045161 single base substitution C T 3_prime_UTR_variant LUSC-KR 9 33045161 33045161 single base substitution C T downstream_gene_variant LUSC-KR 9 33045276 33045276 single base substitution G C 3_prime_UTR_variant LUSC-KR 9 33045276 33045276 single base substitution G C downstream_gene_variant LUSC-KR 9 33047211 33047211 single base substitution A C 3_prime_UTR_variant LUSC-KR 9 33047211 33047211 single base substitution A C downstream_gene_variant LUSC-KR 9 33050119 33050119 single base substitution T C intron_variant LUSC-KR 9 33050848 33050848 single base substitution G A intron_variant LUSC-KR 9 33056299 33056299 single base substitution C T intron_variant LUSC-KR 9 33056303 33056303 single base substitution T G intron_variant LUSC-KR 9 33057316 33057316 single base substitution T C intron_variant LUSC-KR 9 33058737 33058737 single base substitution T C intron_variant LUSC-KR 9 33066135 33066135 single base substitution C A intron_variant LUSC-KR 9 33066920 33066920 single base substitution A G intron_variant LUSC-KR 9 33068768 33068768 single base substitution G A intron_variant LUSC-KR 9 33069062 33069062 single base substitution G A intron_variant LUSC-KR 9 33073175 33073175 single base substitution G A intron_variant LUSC-KR 9 33075091 33075091 single base substitution T A intron_variant LUSC-KR 9 33075331 33075331 single base substitution C A intron_variant LUSC-US 9 33053169 33053169 single base substitution C A synonymous_variant V253V 759G>T LUSC-US 9 33053169 33053169 single base substitution C A synonymous_variant V414V 1242G>T MALY-DE 9 33037325 33037325 single base substitution A C downstream_gene_variant MALY-DE 9 33043678 33043678 single base substitution G A 3_prime_UTR_variant MALY-DE 9 33043678 33043678 single base substitution G A downstream_gene_variant MALY-DE 9 33043723 33043723 single base substitution A G 3_prime_UTR_variant MALY-DE 9 33043723 33043723 single base substitution A G downstream_gene_variant MALY-DE 9 33050495 33050495 single base substitution G A intron_variant MALY-DE 9 33052285 33052285 single base substitution C A intron_variant MALY-DE 9 33052556 33052556 single base substitution G A intron_variant MALY-DE 9 33054688 33054688 single base substitution C T intron_variant MALY-DE 9 33055140 33055140 single base substitution C T intron_variant MALY-DE 9 33056242 33056242 single base substitution C A splice_region_variant MALY-DE 9 33057059 33057059 single base substitution T C intron_variant MALY-DE 9 33062529 33062529 insertion of <=200bp - C intron_variant MALY-DE 9 33068996 33068996 single base substitution T C intron_variant MALY-DE 9 33072857 33072857 single base substitution C A intron_variant MELA-AU 9 33038721 33038721 single base substitution A G downstream_gene_variant MELA-AU 9 33038873 33038873 single base substitution G T downstream_gene_variant MELA-AU 9 33039302 33039302 single base substitution A T downstream_gene_variant MELA-AU 9 33039546 33039546 single base substitution C T downstream_gene_variant MELA-AU 9 33044556 33044556 single base substitution G A 3_prime_UTR_variant MELA-AU 9 33044556 33044556 single base substitution G A downstream_gene_variant MELA-AU 9 33047424 33047424 single base substitution G A intron_variant MELA-AU 9 33048260 33048260 single base substitution G A splice_region_variant MELA-AU 9 33048804 33048804 single base substitution G A intron_variant MELA-AU 9 33049138 33049138 single base substitution G A intron_variant MELA-AU 9 33049271 33049271 single base substitution G A intron_variant MELA-AU 9 33049911 33049911 single base substitution G A intron_variant MELA-AU 9 33049949 33049949 single base substitution G A intron_variant MELA-AU 9 33050615 33050615 single base substitution G A intron_variant MELA-AU 9 33050795 33050795 single base substitution G A intron_variant MELA-AU 9 33050802 33050802 single base substitution G A intron_variant MELA-AU 9 33051180 33051180 single base substitution G A intron_variant MELA-AU 9 33051474 33051474 single base substitution G A intron_variant MELA-AU 9 33051845 33051845 single base substitution G T intron_variant MELA-AU 9 33053061 33053061 single base substitution G A intron_variant MELA-AU 9 33053356 33053356 single base substitution A T intron_variant MELA-AU 9 33053406 33053407 multiple base substitution (>=2bp and <=200bp) GT AA intron_variant MELA-AU 9 33053766 33053766 single base substitution G A intron_variant MELA-AU 9 33054483 33054483 single base substitution G A intron_variant MELA-AU 9 33054953 33054953 single base substitution G A intron_variant MELA-AU 9 33055733 33055733 single base substitution G A intron_variant MELA-AU 9 33055916 33055916 single base substitution G A intron_variant MELA-AU 9 33055918 33055918 single base substitution G A intron_variant MELA-AU 9 33055922 33055923 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 9 33056197 33056197 single base substitution G A missense_variant R185C 553C>T MELA-AU 9 33056197 33056197 single base substitution G A missense_variant R346C 1036C>T MELA-AU 9 33056378 33056378 single base substitution G A intron_variant MELA-AU 9 33059367 33059367 single base substitution G A intron_variant MELA-AU 9 33059395 33059395 single base substitution G C intron_variant MELA-AU 9 33059621 33059621 single base substitution G A intron_variant MELA-AU 9 33060737 33060737 single base substitution G A intron_variant MELA-AU 9 33060738 33060738 single base substitution G T intron_variant MELA-AU 9 33060974 33060974 single base substitution G A intron_variant MELA-AU 9 33060976 33060976 single base substitution G A intron_variant MELA-AU 9 33061141 33061141 single base substitution G A intron_variant MELA-AU 9 33061251 33061251 single base substitution G A intron_variant MELA-AU 9 33062454 33062454 single base substitution A C intron_variant MELA-AU 9 33062790 33062790 single base substitution G A intron_variant MELA-AU 9 33063604 33063604 single base substitution G A intron_variant MELA-AU 9 33063705 33063705 single base substitution G A intron_variant MELA-AU 9 33063869 33063869 single base substitution A T intron_variant MELA-AU 9 33065331 33065331 single base substitution G A intron_variant MELA-AU 9 33066132 33066133 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 9 33068364 33068364 single base substitution G A intron_variant MELA-AU 9 33068693 33068693 single base substitution G A intron_variant MELA-AU 9 33069710 33069710 single base substitution G A intron_variant MELA-AU 9 33069714 33069714 single base substitution T A intron_variant MELA-AU 9 33070759 33070759 single base substitution G A intron_variant MELA-AU 9 33071184 33071184 single base substitution C A intron_variant MELA-AU 9 33073834 33073834 insertion of <=200bp - GA intron_variant MELA-AU 9 33073942 33073942 single base substitution G A intron_variant MELA-AU 9 33075061 33075061 single base substitution G A intron_variant MELA-AU 9 33075191 33075191 single base substitution G C intron_variant MELA-AU 9 33076764 33076764 single base substitution C G upstream_gene_variant MELA-AU 9 33078543 33078543 single base substitution C T upstream_gene_variant MELA-AU 9 33080503 33080503 single base substitution C G upstream_gene_variant MELA-AU 9 33081017 33081017 single base substitution G A upstream_gene_variant ORCA-IN 9 33041417 33041417 single base substitution C T downstream_gene_variant ORCA-IN 9 33041893 33041893 single base substitution T C 3_prime_UTR_variant ORCA-IN 9 33068196 33068196 single base substitution T C intron_variant OV-AU 9 33037599 33037599 single base substitution G C downstream_gene_variant OV-AU 9 33047929 33047929 single base substitution T A intron_variant OV-AU 9 33052199 33052199 single base substitution A C intron_variant OV-AU 9 33055111 33055111 single base substitution G A intron_variant OV-AU 9 33064724 33064724 single base substitution G T intron_variant OV-AU 9 33077090 33077090 single base substitution C T upstream_gene_variant OV-AU 9 33078226 33078226 single base substitution G C upstream_gene_variant PACA-AU 9 33036982 33036982 single base substitution T G downstream_gene_variant PACA-AU 9 33043199 33043199 single base substitution C G 3_prime_UTR_variant PACA-AU 9 33043199 33043199 single base substitution C G downstream_gene_variant PACA-AU 9 33043713 33043713 single base substitution G A 3_prime_UTR_variant PACA-AU 9 33043713 33043713 single base substitution G A downstream_gene_variant PACA-AU 9 33051714 33051714 single base substitution G A intron_variant PACA-AU 9 33062193 33062193 single base substitution A T intron_variant PACA-AU 9 33075315 33075315 single base substitution C G intron_variant PACA-CA 9 33036871 33036871 single base substitution C A downstream_gene_variant PACA-CA 9 33039546 33039546 single base substitution C T downstream_gene_variant PACA-CA 9 33041860 33041860 single base substitution A C 3_prime_UTR_variant PACA-CA 9 33047118 33047118 deletion of <=200bp A - 3_prime_UTR_variant PACA-CA 9 33047118 33047118 deletion of <=200bp A - downstream_gene_variant PACA-CA 9 33050068 33050068 single base substitution C T intron_variant PACA-CA 9 33051738 33051738 single base substitution A C intron_variant PACA-CA 9 33059610 33059610 deletion of <=200bp T - intron_variant PACA-CA 9 33060733 33060733 single base substitution G A intron_variant PACA-CA 9 33063320 33063320 single base substitution A G intron_variant PACA-CA 9 33064116 33064116 single base substitution A T intron_variant PACA-CA 9 33068065 33068065 single base substitution T A intron_variant PACA-CA 9 33071204 33071204 deletion of <=200bp G - intron_variant PACA-CA 9 33071465 33071465 single base substitution C G intron_variant PACA-CA 9 33076108 33076108 single base substitution G A intron_variant PACA-CA 9 33077622 33077622 single base substitution C T upstream_gene_variant PACA-CA 9 33078667 33078667 single base substitution T A upstream_gene_variant PACA-CA 9 33078668 33078668 single base substitution A T upstream_gene_variant PACA-CA 9 33080129 33080129 single base substitution C G upstream_gene_variant PAEN-AU 9 33047164 33047164 single base substitution T C 3_prime_UTR_variant PAEN-AU 9 33047164 33047164 single base substitution T C downstream_gene_variant PAEN-AU 9 33064916 33064916 single base substitution T G intron_variant PAEN-AU 9 33078576 33078576 single base substitution G A upstream_gene_variant PBCA-DE 9 33043731 33043731 single base substitution C A 3_prime_UTR_variant PBCA-DE 9 33043731 33043731 single base substitution C A downstream_gene_variant PBCA-DE 9 33052116 33052119 deletion of <=200bp AAAT - intron_variant PBCA-DE 9 33055482 33055482 insertion of <=200bp - AG intron_variant PBCA-DE 9 33060416 33060416 single base substitution C T intron_variant PBCA-DE 9 33062184 33062184 insertion of <=200bp - A intron_variant PBCA-DE 9 33068845 33068845 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant PBCA-DE 9 33068845 33068845 single base substitution G A missense_variant R160C 478C>T PBCA-DE 9 33075062 33075062 single base substitution C T intron_variant PBCA-DE 9 33079009 33079009 single base substitution C G upstream_gene_variant PRAD-CA 9 33039546 33039546 single base substitution C T downstream_gene_variant PRAD-CA 9 33044770 33044770 single base substitution T G 3_prime_UTR_variant PRAD-CA 9 33044770 33044770 single base substitution T G downstream_gene_variant PRAD-CA 9 33074449 33074449 single base substitution A C intron_variant PRAD-CA 9 33076831 33076831 single base substitution G T upstream_gene_variant PRAD-US 9 33056918 33056918 single base substitution C T synonymous_variant R143R 429G>A PRAD-US 9 33056918 33056918 single base substitution C T synonymous_variant R304R 912G>A RECA-EU 9 33038266 33038266 single base substitution T A downstream_gene_variant RECA-EU 9 33065176 33065176 single base substitution T A intron_variant RECA-EU 9 33078418 33078418 single base substitution A G upstream_gene_variant SKCA-BR 9 33037996 33037998 deletion of <=200bp CTT - downstream_gene_variant SKCA-BR 9 33039960 33039960 single base substitution A T downstream_gene_variant SKCA-BR 9 33045803 33045803 single base substitution A C 3_prime_UTR_variant SKCA-BR 9 33045803 33045803 single base substitution A C downstream_gene_variant SKCA-BR 9 33045804 33045810 deletion of <=200bp CTGCACT - 3_prime_UTR_variant SKCA-BR 9 33045804 33045810 deletion of <=200bp CTGCACT - downstream_gene_variant SKCA-BR 9 33046581 33046582 deletion of <=200bp TA - 3_prime_UTR_variant SKCA-BR 9 33046581 33046582 deletion of <=200bp TA - downstream_gene_variant SKCA-BR 9 33046581 33046583 deletion of <=200bp TAA - 3_prime_UTR_variant SKCA-BR 9 33046581 33046583 deletion of <=200bp TAA - downstream_gene_variant SKCA-BR 9 33048051 33048051 single base substitution A G intron_variant SKCA-BR 9 33051540 33051540 single base substitution T C intron_variant SKCA-BR 9 33052441 33052441 single base substitution C T intron_variant SKCA-BR 9 33054611 33054611 single base substitution G A intron_variant SKCA-BR 9 33056404 33056404 single base substitution C T intron_variant SKCA-BR 9 33060312 33060312 single base substitution T A intron_variant SKCA-BR 9 33060419 33060419 single base substitution G A intron_variant SKCA-BR 9 33060444 33060444 single base substitution C A intron_variant SKCA-BR 9 33061715 33061715 single base substitution G A intron_variant SKCA-BR 9 33064297 33064297 single base substitution G A intron_variant SKCA-BR 9 33065153 33065153 single base substitution C T intron_variant SKCA-BR 9 33066802 33066802 insertion of <=200bp - CA intron_variant SKCA-BR 9 33067495 33067495 insertion of <=200bp - TC intron_variant SKCA-BR 9 33067666 33067666 single base substitution T A intron_variant SKCA-BR 9 33068893 33068893 single base substitution C T 5_prime_UTR_variant SKCA-BR 9 33068893 33068893 single base substitution C T missense_variant A144T 430G>A SKCA-BR 9 33069524 33069524 single base substitution C G intron_variant SKCA-BR 9 33069529 33069529 single base substitution T G intron_variant SKCA-BR 9 33069540 33069540 single base substitution T C intron_variant SKCA-BR 9 33070889 33070889 single base substitution T G intron_variant SKCA-BR 9 33072230 33072230 single base substitution G A intron_variant SKCA-BR 9 33072837 33072837 single base substitution C A intron_variant SKCA-BR 9 33074449 33074449 single base substitution A C intron_variant SKCA-BR 9 33074927 33074927 single base substitution A C intron_variant SKCA-BR 9 33075250 33075250 single base substitution C T intron_variant SKCA-BR 9 33078425 33078425 single base substitution T G upstream_gene_variant SKCM-US 9 33038721 33038721 single base substitution A G downstream_gene_variant SKCM-US 9 33048118 33048118 single base substitution C T missense_variant E316K 946G>A SKCM-US 9 33048118 33048118 single base substitution C T missense_variant E477K 1429G>A SKCM-US 9 33048158 33048158 single base substitution G A synonymous_variant D302D 906C>T SKCM-US 9 33048158 33048158 single base substitution G A synonymous_variant D463D 1389C>T SKCM-US 9 33056197 33056197 single base substitution G A missense_variant R185C 553C>T SKCM-US 9 33056197 33056197 single base substitution G A missense_variant R346C 1036C>T SKCM-US 9 33060542 33060542 single base substitution G T missense_variant P224Q 671C>A SKCM-US 9 33060542 33060542 single base substitution G T missense_variant P63Q 188C>A SKCM-US 9 33062073 33062073 single base substitution G A missense_variant P202S 604C>T SKCM-US 9 33062073 33062073 single base substitution G A missense_variant P41S 121C>T SKCM-US 9 33062139 33062139 single base substitution G A missense_variant P180S 538C>T SKCM-US 9 33062139 33062139 single base substitution G A missense_variant P19S 55C>T SKCM-US 9 33062142 33062142 single base substitution G A missense_variant P179S 535C>T SKCM-US 9 33062142 33062142 single base substitution G A missense_variant P18S 52C>T SKCM-US 9 33068879 33068879 single base substitution G A 5_prime_UTR_variant SKCM-US 9 33068879 33068879 single base substitution G A synonymous_variant A148A 444C>T SKCM-US 9 33073695 33073695 single base substitution T C intron_variant SKCM-US 9 33073695 33073695 single base substitution T C missense_variant S46G 136A>G SKCM-US 9 33076601 33076601 single base substitution C A 5_prime_UTR_variant SKCM-US 9 33076601 33076601 single base substitution C A synonymous_variant S2S 6G>T STAD-US 9 33038770 33038770 single base substitution A G downstream_gene_variant STAD-US 9 33038834 33038834 single base substitution A G downstream_gene_variant STAD-US 9 33053213 33053213 single base substitution C T missense_variant V239I 715G>A STAD-US 9 33053213 33053213 single base substitution C T missense_variant V400I 1198G>A STAD-US 9 33056197 33056197 single base substitution G A missense_variant R185C 553C>T STAD-US 9 33056197 33056197 single base substitution G A missense_variant R346C 1036C>T STAD-US 9 33068845 33068845 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant STAD-US 9 33068845 33068845 single base substitution G A missense_variant R160C 478C>T THCA-SA 9 33043372 33043372 single base substitution T G 3_prime_UTR_variant THCA-SA 9 33043372 33043372 single base substitution T G downstream_gene_variant THCA-SA 9 33068869 33068869 single base substitution C T 5_prime_UTR_variant THCA-SA 9 33068869 33068869 single base substitution C T missense_variant E152K 454G>A THCA-SA 9 33068903 33068903 single base substitution C G 5_prime_UTR_variant THCA-SA 9 33068903 33068903 single base substitution C G missense_variant K140N 420G>C UCEC-US 9 33038709 33038709 single base substitution C A downstream_gene_variant UCEC-US 9 33056946 33056946 single base substitution C A missense_variant S134I 401G>T UCEC-US 9 33056946 33056946 single base substitution C A missense_variant S295I 884G>T UCEC-US 9 33062078 33062078 single base substitution T G missense_variant K200T 599A>C UCEC-US 9 33062078 33062078 single base substitution T G missense_variant K39T 116A>C UCEC-US 9 33073753 33073753 single base substitution C T intron_variant UCEC-US 9 33073753 33073753 single base substitution C T synonymous_variant A26A 78G>A

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-AA-3663-01 COSM1462055 c.1014T>C p.S338S Substitution - coding silent 9:33056221-33056221 - YULONE COSM5410992 c.1463T>A p.I488N Substitution - Missense 9:33047372-33047372 - TCGA-EB-A5UM-01 COSM3656902 c.444C>T p.A148A Substitution - coding silent 9:33068881-33068881 - PTC_212 COSM5958270 c.454G>A p.E152K Substitution - Missense 9:33068871-33068871 - GBM_IV-21 COSM4967080 c.1457A>G p.D486G Substitution - Missense 9:33047378-33047378 - BD230T COSM5496725 c.583G>T p.D195Y Substitution - Missense 9:33062096-33062096 - TCGA-18-3410-01 COSM753620 c.1242G>T p.V414V Substitution - coding silent 9:33053171-33053171 - CN-AML-NR-08-Dx COSM3982819 c.549C>T p.T183T Substitution - coding silent 9:33062130-33062130 - TCGA-RP-A693-06 COSM4895849 c.1429G>A p.E477K Substitution - Missense 9:33048120-33048120 - 587376 COSM1226911 c.553G>A p.D185N Substitution - Missense 9:33062126-33062126 - T3246 COSM4728598 c.408T>C p.S136S Substitution - coding silent 9:33068917-33068917 - TCGA-IR-A3LK-01 COSM4817262 c.198G>A p.L66L Substitution - coding silent 9:33073635-33073635 - I2L-P25-Tumor-Organoid COSM1331578 c.453C>T p.G151G Substitution - coding silent 9:33068872-33068872 - TCGA-ER-A19Q-06 COSM3656901 c.604C>T p.P202S Substitution - Missense 9:33062075-33062075 - BD230T COSM5496726 c.546G>A p.M182I Substitution - Missense 9:33062133-33062133 - PTC_212 COSM5958288 c.420G>C p.K140N Substitution - Missense 9:33068905-33068905 - TCGA-D1-A174-01 COSM1108290 c.78G>A p.A26A Substitution - coding silent 9:33073755-33073755 - EWS834 COSM1108290 c.78G>A p.A26A Substitution - coding silent 9:33073755-33073755 - PT36 COSM5915890 c.1219C>T p.P407S Substitution - Missense 9:33053194-33053194 - YUMOBER COSM3656899 c.1036C>T p.R346C Substitution - Missense 9:33056199-33056199 - CHC1594T COSM4805007 c.451G>T p.G151C Substitution - Missense 9:33068874-33068874 - TCGA-HU-A4GX-01 COSM3656899 c.1036C>T p.R346C Substitution - Missense 9:33056199-33056199 - YUKLAB COSM1701038 c.1157C>T p.T386I Substitution - Missense 9:33053256-33053256 - 2205 COSM5012003 c.304C>A p.P102T Substitution - Missense 9:33071826-33071826 - PT49 COSM5935517 c.1046C>T p.S349F Substitution - Missense 9:33056189-33056189 - HCC7 COSM1624907 c.869T>C p.V290A Substitution - Missense 9:33056963-33056963 - BD230T COSM5496724 c.595G>T p.E199* Substitution - Nonsense 9:33062084-33062084 - SNUH_G10_S1 COSM3982819 c.549C>T p.T183T Substitution - coding silent 9:33062130-33062130 - TCGA-AP-A051-01 COSM1108287 c.884G>T p.S295I Substitution - Missense 9:33056948-33056948 - TCGA-EE-A2MR-06 COSM3656903 c.6G>T p.S2S Substitution - coding silent 9:33076603-33076603 - TCGA-CJ-4900-01 COSM1497074 c.35G>A p.R12H Substitution - Missense 9:33073798-33073798 - HCC7T COSM1624907 c.869T>C p.V290A Substitution - Missense 9:33056963-33056963 - LUAD-S01315 COSM346122 c.449C>G p.A150G Substitution - Missense 9:33068876-33068876 - TCGA-29-1785-01 COSM1331578 c.453C>T p.G151G Substitution - coding silent 9:33068872-33068872 - ICGC_MB53 COSM3765450 c.478C>T p.R160C Substitution - Missense 9:33068847-33068847 - TCGA-GN-A266-06 COSM3926690 c.535C>T p.P179S Substitution - Missense 9:33062144-33062144 - TCGA-G9-6385-01 COSM1132510 c.912G>A p.R304R Substitution - coding silent 9:33056920-33056920 - TCGA-DI-A0WH-01 COSM1108289 c.574G>A p.A192T Substitution - Missense 9:33062105-33062105 - TCGA-A3-3380-01 COSM1497076 c.800T>C p.V267A Substitution - Missense 9:33057665-33057665 - BD230T COSM5496723 c.679C>T p.Q227* Substitution - Nonsense 9:33060536-33060536 - TCGA-61-2104-01 COSM117950 c.644C>A p.S215* Substitution - Nonsense 9:33060571-33060571 - TCGA-G4-6303-01 COSM1462056 c.338G>A p.R113Q Substitution - Missense 9:33071792-33071792 - SNUH_G47_S1 COSM3982818 c.1444-9A>G p.? Unknown 9:33047400-33047400 - TCGA-AC-A23H-01 COSM3848344 c.823G>A p.D275N Substitution - Missense 9:33057642-33057642 - I2L-P7-Tumor-Organoid COSM5359584 c.289T>C p.L97L Substitution - coding silent 9:33071841-33071841 - TCGA-EE-A2MR-06 COSM3656900 c.671C>A p.P224Q Substitution - Missense 9:33060544-33060544 - CN-AML-08-T COSM3982819 c.549C>T p.T183T Substitution - coding silent 9:33062130-33062130 - TCGA-CJ-4875-01 COSM3367687 c.151A>G p.I51V Substitution - Missense 9:33073682-33073682 - TCGA-D9-A1JW-06 COSM3656899 c.1036C>T p.R346C Substitution - Missense 9:33056199-33056199 - CSCC-44-T COSM4457375 c.1042C>T p.H348Y Substitution - Missense 9:33056193-33056193 - TCGA-D9-A6EC-06 COSM4405161 c.136A>G p.S46G Substitution - Missense 9:33073697-33073697 - TCGA-FS-A1ZK-06 COSM3656898 c.1389C>T p.D463D Substitution - coding silent 9:33048160-33048160 - CSCC-55-T COSM4464831 c.1354C>T p.P452S Substitution - Missense 9:33048195-33048195 - TCGA-23-1110-01 COSM69294 c.26+1G>A p.? Unknown 9:33076582-33076582 - TCGA-CG-4436-01 COSM3765450 c.478C>T p.R160C Substitution - Missense 9:33068847-33068847 - Pat_32_A COSM5876114 c.1178C>T p.T393I Substitution - Missense 9:33053235-33053235 - TCGA-CG-5721-01 COSM3906871 c.1198G>A p.V400I Substitution - Missense 9:33053215-33053215 - CSCC-27-T COSM4564679 c.1354_1355CC>TT p.P452F Substitution - Missense 9:33048194-33048195 - RKO COSM2772440 c.173C>A p.T58N Substitution - Missense 9:33073660-33073660 - HT115 COSM2772435 c.636T>C p.G212G Substitution - coding silent 9:33060579-33060579 - T3064 COSM4728599 c.381T>C p.D127D Substitution - coding silent 9:33071749-33071749 - TCGA-B8-5162-01 COSM1497075 c.369G>C p.R123S Substitution - Missense 9:33071761-33071761 - TCGA-AP-A0LM-01 COSM1108288 c.599A>C p.K200T Substitution - Missense 9:33062080-33062080 - PT46 COSM5929146 c.358C>T p.L120F Substitution - Missense 9:33071772-33071772 - C089 COSM5543463 c.1317A>T p.K439N Substitution - Missense 9:33048232-33048232 - TCGA-AY-6197-01 COSM1462052 c.1415T>C p.V472A Substitution - Missense 9:33048134-33048134 - 2171665 COSM4423123 c.192G>T p.Q64H Substitution - Missense 9:33073641-33073641 - 022T COSM1728036 c.158G>A p.S53N Substitution - Missense 9:33073675-33073675 - C086 COSM5539458 c.163C>A p.H55N Substitution - Missense 9:33073670-33073670 - TCGA-AD-6901-01 COSM1462053 c.1179C>T p.T393T Substitution - coding silent 9:33053234-33053234 - CHC1594T COSM4805007 c.451G>T p.G151C Substitution - Missense 9:33068874-33068874 - TCGA-DA-A1HY-06 COSM2772437 c.538C>T p.P180S Substitution - Missense 9:33062141-33062141 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.655350;Hs.655351 9p12 2391418|CGAP|BC002876|A/C|coding|Pro452Thr|1407|Candidate; 2391418|CGAP|BC110654|A/C|coding|Pro452Thr|1501|Candidate; 1731|dbSNP|BC002876|A/G|coding|Arg94Lys|334|Candidate; 1731|dbSNP|BC110654|A/G|coding|Arg94Lys|428|Candidate

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A - IntronicDeletion . c.238-11delT 9 33071901 STAD C A 3-UTRSNV . c.1539+3563G>T 9 33043731 MB C A Synonymous p.V414V c.1242G>T 9 33053169 LUSC C G Missense p.V36L c.106G>C 9 33073725 LUAD C T SpliceDonorSNV . c.26+1G>A 9 33076580 OV C T Synonymous p.A26A c.78G>A 9 33073753 UCEC C T Synonymous p.R304R c.912G>A 9 33056918 PRAD G A Missense p.P179S c.535C>T 9 33062142 CM G A Missense p.P180S c.538C>T 9 33062139 CM G A Missense p.P202S c.604C>T 9 33062073 CM G A Missense p.R160C c.478C>T 9 33068845 MB G A Missense p.R160C c.478C>T 9 33068845 STAD G A Missense p.R346C c.1036C>T 9 33056197 CM G A Synonymous p.D463D c.1389C>T 9 33048158 CM G A Synonymous p.P102P c.306C>T 9 33071822 LUAD G A Synonymous p.T29T c.87C>T 9 33073744 CM G C Missense p.Q213E c.637C>G 9 33060576 MM G T Nonsense p.S215* c.644C>A 9 33060569 OV T C IntronicSNV . c.502-1098A>G 9 33063273 CLL T C Missense p.I51V c.151A>G 9 33073680 RCCC