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 15 74740854 74740854 + Missense_Mutation SNP G G A TCGA-OR-A5KV-01A-11D-A29I-10 TCGA-OR-A5KV-10A-01D-A29L-10 g.chr15:74740854G>A c.970C>T c.(970-972)Cat>Tat p.H324Y BLCA 15 74749005 74749005 + Silent SNP G G T TCGA-DK-A3X1-01A-12D-A22Z-08 TCGA-DK-A3X1-10A-01D-A22Z-08 g.chr15:74749005G>T c.192C>A c.(190-192)atC>atA p.I64I BLCA 15 74751198 74751198 + Missense_Mutation SNP G G A TCGA-DK-A3X1-01A-12D-A22Z-08 TCGA-DK-A3X1-10A-01D-A22Z-08 g.chr15:74751198G>A c.11C>T c.(10-12)tCa>tTa p.S4L BRCA 15 74741602 74741602 + Missense_Mutation SNP C C G TCGA-AC-A3W6-01A-12D-A228-09 TCGA-AC-A3W6-10A-01D-A22A-09 g.chr15:74741602C>G c.807G>C c.(805-807)caG>caC p.Q269H COAD 15 74738556 74738557 + Frame_Shift_Ins INS - - C TCGA-CM-6169-01A-11D-1650-10 TCGA-CM-6169-10A-01D-1650-10 g.chr15:74738556_74738557insC c.1017_1018insG c.(1015-1020)cagcccfs p.P340fs COAD 15 74740842 74740842 + Missense_Mutation SNP C C T TCGA-CK-4950-01A-01D-1719-10 TCGA-CK-4950-10A-01D-1719-10 g.chr15:74740842C>T c.982G>A c.(982-984)Gcc>Acc p.A328T COAD 15 74741655 74741655 + Missense_Mutation SNP G G A TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr15:74741655G>A c.754C>T c.(754-756)Cgc>Tgc p.R252C COAD 15 74742335 74742335 + Missense_Mutation SNP C C T TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr15:74742335C>T c.606G>A c.(604-606)atG>atA p.M202I COAD 15 74743157 74743157 + Silent SNP G G A TCGA-A6-3809-01A-01W-0995-10 TCGA-A6-3809-11A-01W-0995-10 g.chr15:74743157G>A c.516C>T c.(514-516)ccC>ccT p.P172P COAD 15 74751080 74751080 + Silent SNP C C T TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr15:74751080C>T c.129G>A c.(127-129)ctG>ctA p.L43L COAD 15 74751134 74751134 + Silent SNP C C T TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chr15:74751134C>T c.75G>A c.(73-75)ttG>ttA p.L25L COADREAD 15 74738556 74738557 + Frame_Shift_Ins INS - - C TCGA-CM-6169-01A-11D-1650-10 TCGA-CM-6169-10A-01D-1650-10 g.chr15:74738556_74738557insC c.1017_1018insG c.(1015-1020)cagcccfs p.P340fs COADREAD 15 74740842 74740842 + Missense_Mutation SNP C C T TCGA-CK-4950-01A-01D-1719-10 TCGA-CK-4950-10A-01D-1719-10 g.chr15:74740842C>T c.982G>A c.(982-984)Gcc>Acc p.A328T COADREAD 15 74741655 74741655 + Missense_Mutation SNP G G A TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr15:74741655G>A c.754C>T c.(754-756)Cgc>Tgc p.R252C COADREAD 15 74742335 74742335 + Missense_Mutation SNP C C T TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr15:74742335C>T c.606G>A c.(604-606)atG>atA p.M202I COADREAD 15 74743157 74743157 + Silent SNP G G A TCGA-A6-3809-01A-01W-0995-10 TCGA-A6-3809-11A-01W-0995-10 g.chr15:74743157G>A c.516C>T c.(514-516)ccC>ccT p.P172P COADREAD 15 74751080 74751080 + Silent SNP C C T TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr15:74751080C>T c.129G>A c.(127-129)ctG>ctA p.L43L COADREAD 15 74751134 74751134 + Silent SNP C C T TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chr15:74751134C>T c.75G>A c.(73-75)ttG>ttA p.L25L GBMLGG 15 74748994 74748994 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:74748994C>T c.203G>A c.(202-204)cGg>cAg p.R68Q GBMLGG 15 74751068 74751068 + Silent SNP A A G TCGA-DU-5852-01A-11D-1705-08 TCGA-DU-5852-10A-01D-1705-08 g.chr15:74751068A>G c.141T>C c.(139-141)atT>atC p.I47I HNSC 15 74738533 74738533 + Silent SNP G G A TCGA-CN-6022-01A-21D-1683-08 TCGA-CN-6022-10A-01D-1683-08 g.chr15:74738533G>A c.1041C>T c.(1039-1041)gaC>gaT p.D347D HNSC 15 74740855 74740855 + Silent SNP C C T TCGA-CV-7423-01A-11D-2078-08 TCGA-CV-7423-10A-01D-2078-08 g.chr15:74740855C>T c.969G>A c.(967-969)caG>caA p.Q323Q HNSC 15 74741683 74741683 + Silent SNP G G A TCGA-RS-A6TO-01A-32D-A34J-08 TCGA-RS-A6TO-10A-01D-A34M-08 g.chr15:74741683G>A c.726C>T c.(724-726)tcC>tcT p.S242S HNSC 15 74748953 74748953 + Nonsense_Mutation SNP G G A TCGA-IQ-A61E-01A-22D-A30E-08 TCGA-IQ-A61E-10A-01D-A30H-08 g.chr15:74748953G>A c.244C>T c.(244-246)Caa>Taa p.Q82* KIPAN 15 74742277 74742277 + Splice_Site SNP C C G TCGA-SX-A7SP-01A-11D-A34Z-10 TCGA-SX-A7SP-10A-01D-A34Z-10 g.chr15:74742277C>G c.664G>C c.(664-666)Ggt>Cgt p.G222R KIRP 15 74742277 74742277 + Splice_Site SNP C C G TCGA-SX-A7SP-01A-11D-A34Z-10 TCGA-SX-A7SP-10A-01D-A34Z-10 g.chr15:74742277C>G c.664G>C c.(664-666)Ggt>Cgt p.G222R LGG 15 74748994 74748994 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:74748994C>T c.203G>A c.(202-204)cGg>cAg p.R68Q LGG 15 74751068 74751068 + Silent SNP A A G TCGA-DU-5852-01A-11D-1705-08 TCGA-DU-5852-10A-01D-1705-08 g.chr15:74751068A>G c.141T>C c.(139-141)atT>atC p.I47I LIHC 15 74742014 74742014 + Missense_Mutation SNP C C A TCGA-G3-A5SJ-01A-11D-A27I-10 TCGA-G3-A5SJ-10A-01D-A27I-10 g.chr15:74742014C>A c.667G>T c.(667-669)Ggc>Tgc p.G223C LUSC 15 74738472 74738472 + Nonsense_Mutation SNP G G A TCGA-22-5473-01A-01D-1632-08 TCGA-22-5473-11A-11D-1632-08 g.chr15:74738472G>A c.1102C>T c.(1102-1104)Caa>Taa p.Q368* LUSC 15 74751086 74751086 + Silent SNP T T A TCGA-22-5477-01A-01D-1632-08 TCGA-22-5477-11A-11D-1632-08 g.chr15:74751086T>A c.123A>T c.(121-123)tcA>tcT p.S41S OV 15 74743861 74743861 + Splice_Site SNP C C T TCGA-23-1028-01A-01W-0484-10 TCGA-23-1028-10B-01W-0484-10 g.chr15:74743861C>T c.388G>A c.(388-390)Gtc>Atc p.V130I PAAD 15 74743165 74743165 + Missense_Mutation SNP C C A TCGA-FB-AAQ2-01A-31D-A40W-08 TCGA-FB-AAQ2-11A-11D-A40W-08 g.chr15:74743165C>A c.508G>T c.(508-510)Gct>Tct p.A170S PRAD 15 74744688 74744689 + Frame_Shift_Del DEL CT CT - TCGA-ZG-A9L5-01A-12D-A41K-08 TCGA-ZG-A9L5-10A-01D-A41N-08 g.chr15:74744688_74744689delCT c.335_336delAG c.(334-336)gagfs p.E112fs SKCM 15 74738569 74738569 + Splice_Site SNP C C T TCGA-EE-A2GM-06B-11D-A196-08 TCGA-EE-A2GM-10A-01D-A198-08 g.chr15:74738569C>T c.e11-1 SKCM 15 74740848 74740848 + Missense_Mutation SNP G G A TCGA-ER-A19E-06A-11D-A197-08 TCGA-ER-A19E-10A-01D-A199-08 g.chr15:74740848G>A c.976C>T c.(976-978)Ctt>Ttt p.L326F SKCM 15 74740913 74740913 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr15:74740913G>A c.911C>T c.(910-912)tCc>tTc p.S304F SKCM 15 74741550 74741550 + Missense_Mutation SNP G G A TCGA-QB-A6FS-06A-11D-A30X-08 TCGA-QB-A6FS-10A-01D-A30X-08 g.chr15:74741550G>A c.859C>T c.(859-861)Cac>Tac p.H287Y SKCM 15 74741678 74741678 + Missense_Mutation SNP G G A TCGA-FS-A1ZZ-06A-11D-A197-08 TCGA-FS-A1ZZ-10A-01D-A199-08 g.chr15:74741678G>A c.731C>T c.(730-732)cCc>cTc p.P244L SKCM 15 74742300 74742300 + Missense_Mutation SNP G G A TCGA-EE-A2GJ-06A-11D-A196-08 TCGA-EE-A2GJ-10A-01D-A198-08 g.chr15:74742300G>A c.641C>T c.(640-642)tCc>tTc p.S214F SKCM 15 74742300 74742300 + Missense_Mutation SNP G G A TCGA-ER-A195-06A-11D-A196-08 TCGA-ER-A195-10A-01D-A198-08 g.chr15:74742300G>A c.641C>T c.(640-642)tCc>tTc p.S214F SKCM 15 74742405 74742405 + Missense_Mutation SNP A A C TCGA-D3-A5GO-06A-12D-A27K-08 TCGA-D3-A5GO-10A-01D-A27N-08 g.chr15:74742405A>C c.536T>G c.(535-537)gTg>gGg p.V179G SKCM 15 74743147 74743147 + Missense_Mutation SNP C C T TCGA-EE-A2A1-06A-11D-A197-08 TCGA-EE-A2A1-10A-01D-A199-08 g.chr15:74743147C>T c.526G>A c.(526-528)Gat>Aat p.D176N SKCM 15 74743820 74743820 + Silent SNP G G A TCGA-ER-A19F-06A-11D-A196-08 TCGA-ER-A19F-10A-01D-A198-08 g.chr15:74743820G>A c.429C>T c.(427-429)atC>atT p.I143I SKCM 15 74751147 74751147 + Missense_Mutation SNP G G A TCGA-ER-A3PL-06A-11D-A23B-08 TCGA-ER-A3PL-10A-01D-A23B-08 g.chr15:74751147G>A c.62C>T c.(61-63)tCt>tTt p.S21F

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 15 74749005 74749005 single base substitution G T synonymous_variant I64I 192C>A BLCA-US 15 74749005 74749005 single base substitution G T upstream_gene_variant BLCA-US 15 74751198 74751198 single base substitution G A missense_variant S4L 11C>T BRCA-EU 15 74734406 74734406 single base substitution C G downstream_gene_variant BRCA-EU 15 74735426 74735426 single base substitution C G downstream_gene_variant BRCA-EU 15 74735570 74735570 insertion of <=200bp - T downstream_gene_variant BRCA-EU 15 74739247 74739247 single base substitution G C downstream_gene_variant BRCA-EU 15 74739247 74739247 single base substitution G C intron_variant BRCA-EU 15 74739353 74739353 deletion of <=200bp A - downstream_gene_variant BRCA-EU 15 74739353 74739353 deletion of <=200bp A - intron_variant BRCA-EU 15 74740046 74740046 insertion of <=200bp - TCAA downstream_gene_variant BRCA-EU 15 74740046 74740046 insertion of <=200bp - TCAA intron_variant BRCA-EU 15 74744746 74744746 single base substitution C G intron_variant BRCA-EU 15 74744746 74744746 single base substitution C G upstream_gene_variant BRCA-EU 15 74746279 74746279 single base substitution G C intron_variant BRCA-EU 15 74746279 74746279 single base substitution G C upstream_gene_variant BRCA-EU 15 74746553 74746553 single base substitution G A intron_variant BRCA-EU 15 74746553 74746553 single base substitution G A upstream_gene_variant BRCA-EU 15 74747524 74747524 single base substitution G A intron_variant BRCA-EU 15 74747524 74747524 single base substitution G A upstream_gene_variant BRCA-EU 15 74747529 74747529 single base substitution G C intron_variant BRCA-EU 15 74747529 74747529 single base substitution G C upstream_gene_variant BRCA-EU 15 74748311 74748311 deletion of <=200bp A - intron_variant BRCA-EU 15 74748311 74748311 deletion of <=200bp A - upstream_gene_variant BRCA-EU 15 74748566 74748566 single base substitution G C intron_variant BRCA-EU 15 74748566 74748566 single base substitution G C upstream_gene_variant BRCA-EU 15 74748837 74748837 single base substitution C A intron_variant BRCA-EU 15 74748837 74748837 single base substitution C A upstream_gene_variant BRCA-EU 15 74748902 74748902 single base substitution G C missense_variant Q99E 295C>G BRCA-EU 15 74748902 74748902 single base substitution G C upstream_gene_variant BRCA-EU 15 74749162 74749162 single base substitution T G intron_variant BRCA-EU 15 74749162 74749162 single base substitution T G upstream_gene_variant BRCA-EU 15 74751029 74751029 single base substitution C G synonymous_variant L60L 180G>C BRCA-EU 15 74751070 74751070 single base substitution T C missense_variant I47V 139A>G BRCA-EU 15 74752198 74752198 single base substitution C T intron_variant BRCA-EU 15 74752652 74752652 single base substitution A G intron_variant BRCA-EU 15 74752753 74752753 single base substitution A G intron_variant BRCA-EU 15 74753205 74753205 single base substitution G T 5_prime_UTR_variant BRCA-EU 15 74753205 74753205 single base substitution G T intron_variant BRCA-EU 15 74753333 74753333 single base substitution G C 5_prime_UTR_premature_start_codon_gain_variant BRCA-EU 15 74753333 74753333 single base substitution G C intron_variant BRCA-EU 15 74754056 74754056 single base substitution C G upstream_gene_variant BRCA-EU 15 74754960 74754960 single base substitution C T upstream_gene_variant BRCA-EU 15 74755194 74755194 single base substitution G A upstream_gene_variant BRCA-EU 15 74755786 74755786 single base substitution C T upstream_gene_variant BRCA-EU 15 74757184 74757184 single base substitution G A upstream_gene_variant BRCA-EU 15 74757381 74757381 single base substitution C A upstream_gene_variant BRCA-EU 15 74757511 74757511 single base substitution C T upstream_gene_variant BRCA-EU 15 74758133 74758133 single base substitution G A upstream_gene_variant BRCA-FR 15 74740144 74740144 single base substitution C A downstream_gene_variant BRCA-FR 15 74740144 74740144 single base substitution C A intron_variant BRCA-FR 15 74755194 74755194 single base substitution G A upstream_gene_variant BRCA-FR 15 74757184 74757184 single base substitution G A upstream_gene_variant BRCA-US 15 74741602 74741602 single base substitution C G downstream_gene_variant BRCA-US 15 74741602 74741602 single base substitution C G intron_variant BRCA-US 15 74741602 74741602 single base substitution C G missense_variant Q17H 51G>C BRCA-US 15 74741602 74741602 single base substitution C G missense_variant Q213H 639G>C BRCA-US 15 74741602 74741602 single base substitution C G missense_variant Q269H 807G>C BTCA-JP 15 74741587 74741587 single base substitution G A downstream_gene_variant BTCA-JP 15 74741587 74741587 single base substitution G A intron_variant BTCA-JP 15 74741587 74741587 single base substitution G A synonymous_variant T218T 654C>T BTCA-JP 15 74741587 74741587 single base substitution G A synonymous_variant T22T 66C>T BTCA-JP 15 74741587 74741587 single base substitution G A synonymous_variant T274T 822C>T BTCA-JP 15 74743138 74743138 single base substitution C T splice_region_variant BTCA-JP 15 74743138 74743138 single base substitution C T upstream_gene_variant CESC-US 15 74753949 74753949 single base substitution C G upstream_gene_variant CESC-US 15 74758431 74758431 single base substitution C T upstream_gene_variant CLLE-ES 15 74739067 74739067 single base substitution T C downstream_gene_variant CLLE-ES 15 74739067 74739067 single base substitution T C intron_variant COAD-US 15 74738556 74738556 insertion of <=200bp - C downstream_gene_variant COAD-US 15 74738556 74738556 insertion of <=200bp - C frameshift_variant P141R? COAD-US 15 74738556 74738556 insertion of <=200bp - C frameshift_variant P340R? COAD-US 15 74738556 74738556 insertion of <=200bp - C frameshift_variant P74R? COAD-US 15 74740842 74740842 single base substitution C T downstream_gene_variant COAD-US 15 74740842 74740842 single base substitution C T intron_variant COAD-US 15 74740842 74740842 single base substitution C T missense_variant A328T 982G>A COAD-US 15 74740842 74740842 single base substitution C T missense_variant A62T 184G>A COAD-US 15 74741655 74741655 single base substitution G A downstream_gene_variant COAD-US 15 74741655 74741655 single base substitution G A intron_variant COAD-US 15 74741655 74741655 single base substitution G A missense_variant R196C 586C>T COAD-US 15 74741655 74741655 single base substitution G A missense_variant R252C 754C>T COAD-US 15 74741655 74741655 single base substitution G A upstream_gene_variant COAD-US 15 74751080 74751080 single base substitution C T synonymous_variant L43L 129G>A COCA-CN 15 74753147 74753147 single base substitution G A 5_prime_UTR_variant COCA-CN 15 74753147 74753147 single base substitution G A intron_variant COCA-CN 15 74753212 74753212 single base substitution G T 5_prime_UTR_variant COCA-CN 15 74753212 74753212 single base substitution G T intron_variant ESAD-UK 15 74733406 74733406 single base substitution C T downstream_gene_variant ESAD-UK 15 74733633 74733633 single base substitution C T downstream_gene_variant ESAD-UK 15 74736449 74736449 single base substitution A T downstream_gene_variant ESAD-UK 15 74739247 74739247 single base substitution G T downstream_gene_variant ESAD-UK 15 74739247 74739247 single base substitution G T intron_variant ESAD-UK 15 74739353 74739353 insertion of <=200bp - A downstream_gene_variant ESAD-UK 15 74739353 74739353 insertion of <=200bp - A intron_variant ESAD-UK 15 74742026 74742026 single base substitution G A downstream_gene_variant ESAD-UK 15 74742026 74742026 single base substitution G A intron_variant ESAD-UK 15 74742026 74742026 single base substitution G A upstream_gene_variant ESAD-UK 15 74743480 74743480 single base substitution T C intron_variant ESAD-UK 15 74743480 74743480 single base substitution T C upstream_gene_variant ESAD-UK 15 74743579 74743579 single base substitution A G intron_variant ESAD-UK 15 74743579 74743579 single base substitution A G upstream_gene_variant ESAD-UK 15 74744169 74744169 single base substitution T G intron_variant ESAD-UK 15 74744169 74744169 single base substitution T G upstream_gene_variant ESAD-UK 15 74744754 74744754 single base substitution G A intron_variant ESAD-UK 15 74744754 74744754 single base substitution G A upstream_gene_variant ESAD-UK 15 74744845 74744845 single base substitution C T intron_variant ESAD-UK 15 74744845 74744845 single base substitution C T upstream_gene_variant ESAD-UK 15 74745716 74745716 single base substitution G A intron_variant ESAD-UK 15 74745716 74745716 single base substitution G A upstream_gene_variant ESAD-UK 15 74746217 74746217 single base substitution T C intron_variant ESAD-UK 15 74746217 74746217 single base substitution T C upstream_gene_variant ESAD-UK 15 74747336 74747336 single base substitution T C intron_variant ESAD-UK 15 74747336 74747336 single base substitution T C upstream_gene_variant ESAD-UK 15 74748352 74748352 single base substitution C T intron_variant ESAD-UK 15 74748352 74748352 single base substitution C T upstream_gene_variant ESAD-UK 15 74748526 74748526 single base substitution C A intron_variant ESAD-UK 15 74748526 74748526 single base substitution C A upstream_gene_variant ESAD-UK 15 74749075 74749075 single base substitution C T intron_variant ESAD-UK 15 74749075 74749075 single base substitution C T upstream_gene_variant ESAD-UK 15 74750724 74750724 single base substitution C T intron_variant ESAD-UK 15 74753928 74753928 single base substitution C T upstream_gene_variant ESAD-UK 15 74755519 74755519 single base substitution C A upstream_gene_variant LAML-KR 15 74750946 74750946 single base substitution T C intron_variant LGG-US 15 74751068 74751068 single base substitution A G synonymous_variant I47I 141T>C LICA-CN 15 74751117 74751117 single base substitution C G missense_variant G31A 92G>C LICA-FR 15 74746172 74746172 single base substitution T C intron_variant LICA-FR 15 74746172 74746172 single base substitution T C upstream_gene_variant LICA-FR 15 74751185 74751185 single base substitution C T synonymous_variant L8L 24G>A LINC-JP 15 74734560 74734560 single base substitution T A downstream_gene_variant LINC-JP 15 74740182 74740182 single base substitution G A downstream_gene_variant LINC-JP 15 74740182 74740182 single base substitution G A intron_variant LINC-JP 15 74743803 74743803 single base substitution C T intron_variant LINC-JP 15 74743803 74743803 single base substitution C T missense_variant G149D 446G>A LINC-JP 15 74743803 74743803 single base substitution C T missense_variant G47D 140G>A LINC-JP 15 74743803 74743803 single base substitution C T upstream_gene_variant LINC-JP 15 74743893 74743893 single base substitution C T intron_variant LINC-JP 15 74743893 74743893 single base substitution C T upstream_gene_variant LINC-JP 15 74751148 74751148 single base substitution A G missense_variant S21P 61T>C LINC-JP 15 74757648 74757648 single base substitution T C upstream_gene_variant LIRI-JP 15 74733602 74733602 single base substitution C T downstream_gene_variant LIRI-JP 15 74735758 74735758 single base substitution T G downstream_gene_variant LIRI-JP 15 74735779 74735779 single base substitution A G downstream_gene_variant LIRI-JP 15 74739587 74739587 single base substitution T C downstream_gene_variant LIRI-JP 15 74739587 74739587 single base substitution T C intron_variant LIRI-JP 15 74740745 74740745 single base substitution G A downstream_gene_variant LIRI-JP 15 74740745 74740745 single base substitution G A intron_variant LIRI-JP 15 74743342 74743342 single base substitution C T intron_variant LIRI-JP 15 74743342 74743342 single base substitution C T upstream_gene_variant LIRI-JP 15 74743560 74743569 deletion of <=200bp TACCCTTATT - intron_variant LIRI-JP 15 74743560 74743569 deletion of <=200bp TACCCTTATT - upstream_gene_variant LIRI-JP 15 74746795 74746795 single base substitution A T intron_variant LIRI-JP 15 74746795 74746795 single base substitution A T upstream_gene_variant LIRI-JP 15 74749966 74749966 single base substitution T C intron_variant LIRI-JP 15 74751212 74751212 single base substitution C T 5_prime_UTR_variant LIRI-JP 15 74756264 74756264 single base substitution C A upstream_gene_variant LIRI-JP 15 74758071 74758071 single base substitution A G upstream_gene_variant LUSC-KR 15 74734691 74734691 single base substitution G A downstream_gene_variant LUSC-KR 15 74734780 74734780 single base substitution C G downstream_gene_variant LUSC-KR 15 74737113 74737113 single base substitution C T downstream_gene_variant LUSC-KR 15 74741015 74741015 single base substitution A G downstream_gene_variant LUSC-KR 15 74741015 74741015 single base substitution A G intron_variant LUSC-KR 15 74741064 74741064 single base substitution A C downstream_gene_variant LUSC-KR 15 74741064 74741064 single base substitution A C intron_variant LUSC-KR 15 74742468 74742468 single base substitution A G intron_variant LUSC-KR 15 74742468 74742468 single base substitution A G upstream_gene_variant LUSC-KR 15 74744298 74744298 single base substitution C T intron_variant LUSC-KR 15 74744298 74744298 single base substitution C T upstream_gene_variant LUSC-KR 15 74749015 74749015 single base substitution A G splice_region_variant LUSC-KR 15 74749015 74749015 single base substitution A G upstream_gene_variant LUSC-US 15 74738472 74738472 single base substitution G A downstream_gene_variant LUSC-US 15 74738472 74738472 single base substitution G A stop_gained Q102* 304C>T LUSC-US 15 74738472 74738472 single base substitution G A stop_gained Q169* 505C>T LUSC-US 15 74738472 74738472 single base substitution G A stop_gained Q368* 1102C>T LUSC-US 15 74751086 74751086 single base substitution T A synonymous_variant S41S 123A>T MALY-DE 15 74738458 74738458 single base substitution C T downstream_gene_variant MALY-DE 15 74738458 74738458 single base substitution C T synonymous_variant E106E 318G>A MALY-DE 15 74738458 74738458 single base substitution C T synonymous_variant E173E 519G>A MALY-DE 15 74738458 74738458 single base substitution C T synonymous_variant E372E 1116G>A MALY-DE 15 74744845 74744845 single base substitution C T intron_variant MALY-DE 15 74744845 74744845 single base substitution C T upstream_gene_variant MALY-DE 15 74752882 74752882 single base substitution C A intron_variant MELA-AU 15 74733425 74733425 single base substitution G A downstream_gene_variant MELA-AU 15 74733863 74733863 single base substitution G A downstream_gene_variant MELA-AU 15 74733986 74733986 single base substitution C T downstream_gene_variant MELA-AU 15 74734002 74734003 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 15 74734335 74734335 single base substitution C T downstream_gene_variant MELA-AU 15 74734640 74734640 single base substitution G A downstream_gene_variant MELA-AU 15 74734901 74734901 single base substitution C T downstream_gene_variant MELA-AU 15 74735052 74735052 single base substitution C A downstream_gene_variant MELA-AU 15 74736260 74736260 single base substitution G A downstream_gene_variant MELA-AU 15 74736265 74736265 single base substitution A G downstream_gene_variant MELA-AU 15 74736449 74736449 single base substitution A T downstream_gene_variant MELA-AU 15 74736540 74736540 single base substitution G C downstream_gene_variant MELA-AU 15 74736634 74736634 single base substitution G A downstream_gene_variant MELA-AU 15 74736895 74736896 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 15 74737299 74737299 single base substitution C A downstream_gene_variant MELA-AU 15 74737299 74737300 multiple base substitution (>=2bp and <=200bp) CC GT downstream_gene_variant MELA-AU 15 74737505 74737505 single base substitution G A downstream_gene_variant MELA-AU 15 74737782 74737782 single base substitution G A downstream_gene_variant MELA-AU 15 74737784 74737784 single base substitution G A downstream_gene_variant MELA-AU 15 74738067 74738067 single base substitution G C downstream_gene_variant MELA-AU 15 74738297 74738297 single base substitution G A downstream_gene_variant MELA-AU 15 74738654 74738654 single base substitution G A downstream_gene_variant MELA-AU 15 74738654 74738654 single base substitution G A intron_variant MELA-AU 15 74738668 74738668 single base substitution C T downstream_gene_variant MELA-AU 15 74738668 74738668 single base substitution C T intron_variant MELA-AU 15 74739166 74739166 single base substitution G A downstream_gene_variant MELA-AU 15 74739166 74739166 single base substitution G A intron_variant MELA-AU 15 74739680 74739680 single base substitution G A downstream_gene_variant MELA-AU 15 74739680 74739680 single base substitution G A intron_variant MELA-AU 15 74739865 74739865 single base substitution G A downstream_gene_variant MELA-AU 15 74739865 74739865 single base substitution G A intron_variant MELA-AU 15 74740182 74740183 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 15 74740182 74740183 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 74740910 74740910 single base substitution G A downstream_gene_variant MELA-AU 15 74740910 74740910 single base substitution G A intron_variant MELA-AU 15 74740910 74740910 single base substitution G A missense_variant S305F 914C>T MELA-AU 15 74741044 74741044 single base substitution A G downstream_gene_variant MELA-AU 15 74741044 74741044 single base substitution A G intron_variant MELA-AU 15 74741404 74741405 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 15 74741404 74741405 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 74741645 74741645 single base substitution G A downstream_gene_variant MELA-AU 15 74741645 74741645 single base substitution G A intron_variant MELA-AU 15 74741645 74741645 single base substitution G A missense_variant S199F 596C>T MELA-AU 15 74741645 74741645 single base substitution G A missense_variant S255F 764C>T MELA-AU 15 74741645 74741645 single base substitution G A missense_variant S3F 8C>T MELA-AU 15 74741810 74741810 single base substitution G A downstream_gene_variant MELA-AU 15 74741810 74741810 single base substitution G A intron_variant MELA-AU 15 74741810 74741810 single base substitution G A upstream_gene_variant MELA-AU 15 74741840 74741840 single base substitution G A downstream_gene_variant MELA-AU 15 74741840 74741840 single base substitution G A intron_variant MELA-AU 15 74741840 74741840 single base substitution G A upstream_gene_variant MELA-AU 15 74741962 74741962 single base substitution C T downstream_gene_variant MELA-AU 15 74741962 74741962 single base substitution C T splice_region_variant MELA-AU 15 74741962 74741962 single base substitution C T upstream_gene_variant MELA-AU 15 74742023 74742023 single base substitution G A downstream_gene_variant MELA-AU 15 74742023 74742023 single base substitution G A splice_region_variant MELA-AU 15 74742023 74742023 single base substitution G A upstream_gene_variant MELA-AU 15 74742045 74742045 single base substitution G A downstream_gene_variant MELA-AU 15 74742045 74742045 single base substitution G A intron_variant MELA-AU 15 74742045 74742045 single base substitution G A upstream_gene_variant MELA-AU 15 74742125 74742125 single base substitution G A downstream_gene_variant MELA-AU 15 74742125 74742125 single base substitution G A intron_variant MELA-AU 15 74742125 74742125 single base substitution G A upstream_gene_variant MELA-AU 15 74742446 74742446 single base substitution C T intron_variant MELA-AU 15 74742446 74742446 single base substitution C T upstream_gene_variant MELA-AU 15 74742658 74742659 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 74742658 74742659 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 15 74742776 74742776 single base substitution G A intron_variant MELA-AU 15 74742776 74742776 single base substitution G A upstream_gene_variant MELA-AU 15 74743103 74743103 single base substitution G A intron_variant MELA-AU 15 74743103 74743103 single base substitution G A upstream_gene_variant MELA-AU 15 74743154 74743154 single base substitution A G missense_variant I145T 434T>C MELA-AU 15 74743154 74743154 single base substitution A G synonymous_variant N117N 351T>C MELA-AU 15 74743154 74743154 single base substitution A G synonymous_variant N173N 519T>C MELA-AU 15 74743154 74743154 single base substitution A G synonymous_variant N71N 213T>C MELA-AU 15 74743154 74743154 single base substitution A G upstream_gene_variant MELA-AU 15 74743159 74743159 single base substitution G A missense_variant P116S 346C>T MELA-AU 15 74743159 74743159 single base substitution G A missense_variant P172S 514C>T MELA-AU 15 74743159 74743159 single base substitution G A missense_variant P70S 208C>T MELA-AU 15 74743159 74743159 single base substitution G A synonymous_variant I143I 429C>T MELA-AU 15 74743159 74743159 single base substitution G A upstream_gene_variant MELA-AU 15 74743446 74743446 single base substitution G C intron_variant MELA-AU 15 74743446 74743446 single base substitution G C upstream_gene_variant MELA-AU 15 74743514 74743514 single base substitution G A intron_variant MELA-AU 15 74743514 74743514 single base substitution G A upstream_gene_variant MELA-AU 15 74743739 74743739 single base substitution G A intron_variant MELA-AU 15 74743739 74743739 single base substitution G A upstream_gene_variant MELA-AU 15 74743833 74743833 single base substitution G A intron_variant MELA-AU 15 74743833 74743833 single base substitution G A missense_variant S139F 416C>T MELA-AU 15 74743833 74743833 single base substitution G A missense_variant S37F 110C>T MELA-AU 15 74743833 74743833 single base substitution G A upstream_gene_variant MELA-AU 15 74743978 74743978 single base substitution G A intron_variant MELA-AU 15 74743978 74743978 single base substitution G A upstream_gene_variant MELA-AU 15 74744617 74744618 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 74744617 74744618 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 15 74744718 74744718 single base substitution T C 5_prime_UTR_variant MELA-AU 15 74744718 74744718 single base substitution T C intron_variant MELA-AU 15 74744718 74744718 single base substitution T C splice_region_variant MELA-AU 15 74744718 74744718 single base substitution T C upstream_gene_variant MELA-AU 15 74745133 74745133 single base substitution A G intron_variant MELA-AU 15 74745133 74745133 single base substitution A G upstream_gene_variant MELA-AU 15 74745617 74745617 single base substitution G A intron_variant MELA-AU 15 74745617 74745617 single base substitution G A upstream_gene_variant MELA-AU 15 74745760 74745760 single base substitution G A intron_variant MELA-AU 15 74745760 74745760 single base substitution G A upstream_gene_variant MELA-AU 15 74746022 74746022 single base substitution G A intron_variant MELA-AU 15 74746022 74746022 single base substitution G A upstream_gene_variant MELA-AU 15 74746565 74746565 single base substitution G A intron_variant MELA-AU 15 74746565 74746565 single base substitution G A upstream_gene_variant MELA-AU 15 74747649 74747649 single base substitution G A intron_variant MELA-AU 15 74747649 74747649 single base substitution G A upstream_gene_variant MELA-AU 15 74748024 74748024 single base substitution G A intron_variant MELA-AU 15 74748024 74748024 single base substitution G A upstream_gene_variant MELA-AU 15 74748237 74748237 single base substitution G A intron_variant MELA-AU 15 74748237 74748237 single base substitution G A upstream_gene_variant MELA-AU 15 74748258 74748258 single base substitution G A intron_variant MELA-AU 15 74748258 74748258 single base substitution G A upstream_gene_variant MELA-AU 15 74748455 74748455 single base substitution G A intron_variant MELA-AU 15 74748455 74748455 single base substitution G A upstream_gene_variant MELA-AU 15 74748651 74748651 single base substitution C T intron_variant MELA-AU 15 74748651 74748651 single base substitution C T upstream_gene_variant MELA-AU 15 74749177 74749177 single base substitution G A intron_variant MELA-AU 15 74749177 74749177 single base substitution G A upstream_gene_variant MELA-AU 15 74749594 74749594 single base substitution G A intron_variant MELA-AU 15 74749594 74749594 single base substitution G A upstream_gene_variant MELA-AU 15 74749909 74749909 single base substitution T C intron_variant MELA-AU 15 74750562 74750562 single base substitution G A intron_variant MELA-AU 15 74750630 74750630 single base substitution G A intron_variant MELA-AU 15 74750680 74750680 single base substitution G A intron_variant MELA-AU 15 74751705 74751705 single base substitution G A intron_variant MELA-AU 15 74751880 74751880 single base substitution G A intron_variant MELA-AU 15 74753514 74753514 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 15 74753514 74753514 single base substitution G A upstream_gene_variant MELA-AU 15 74753515 74753515 single base substitution G A 5_prime_UTR_variant MELA-AU 15 74753515 74753515 single base substitution G A upstream_gene_variant MELA-AU 15 74753521 74753521 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant MELA-AU 15 74753521 74753521 single base substitution G A upstream_gene_variant MELA-AU 15 74753528 74753528 single base substitution C T upstream_gene_variant MELA-AU 15 74753555 74753555 single base substitution C T upstream_gene_variant MELA-AU 15 74753569 74753569 single base substitution C T upstream_gene_variant MELA-AU 15 74753844 74753844 single base substitution C T upstream_gene_variant MELA-AU 15 74753865 74753865 single base substitution C T upstream_gene_variant MELA-AU 15 74755902 74755902 single base substitution A G upstream_gene_variant MELA-AU 15 74756145 74756145 single base substitution C T upstream_gene_variant MELA-AU 15 74756160 74756160 single base substitution C T upstream_gene_variant MELA-AU 15 74757046 74757046 single base substitution C T upstream_gene_variant MELA-AU 15 74757131 74757131 single base substitution C T upstream_gene_variant MELA-AU 15 74757394 74757394 single base substitution C T upstream_gene_variant MELA-AU 15 74757577 74757577 single base substitution T C upstream_gene_variant MELA-AU 15 74757674 74757674 single base substitution C T upstream_gene_variant MELA-AU 15 74757675 74757675 single base substitution C T upstream_gene_variant MELA-AU 15 74757860 74757860 single base substitution C T upstream_gene_variant MELA-AU 15 74757967 74757967 single base substitution C T upstream_gene_variant MELA-AU 15 74758250 74758250 single base substitution C T upstream_gene_variant MELA-AU 15 74758287 74758287 single base substitution C T upstream_gene_variant OV-AU 15 74757504 74757504 single base substitution C A upstream_gene_variant PACA-AU 15 74736448 74736448 single base substitution T A downstream_gene_variant PACA-AU 15 74749042 74749042 single base substitution G A intron_variant PACA-AU 15 74749042 74749042 single base substitution G A upstream_gene_variant PACA-AU 15 74749043 74749043 single base substitution C A intron_variant PACA-AU 15 74749043 74749043 single base substitution C A upstream_gene_variant PACA-AU 15 74750276 74750276 single base substitution T A intron_variant PACA-CA 15 74734843 74734843 single base substitution A G downstream_gene_variant PACA-CA 15 74736449 74736449 single base substitution A T downstream_gene_variant PACA-CA 15 74738501 74738501 single base substitution C T downstream_gene_variant PACA-CA 15 74738501 74738501 single base substitution C T missense_variant R159Q 476G>A PACA-CA 15 74738501 74738501 single base substitution C T missense_variant R358Q 1073G>A PACA-CA 15 74738501 74738501 single base substitution C T missense_variant R92Q 275G>A PACA-CA 15 74739353 74739353 deletion of <=200bp A - downstream_gene_variant PACA-CA 15 74739353 74739353 deletion of <=200bp A - intron_variant PACA-CA 15 74739571 74739571 single base substitution C T downstream_gene_variant PACA-CA 15 74739571 74739571 single base substitution C T intron_variant PACA-CA 15 74740027 74740027 single base substitution G A downstream_gene_variant PACA-CA 15 74740027 74740027 single base substitution G A intron_variant PACA-CA 15 74741168 74741168 single base substitution C T downstream_gene_variant PACA-CA 15 74741168 74741168 single base substitution C T intron_variant PACA-CA 15 74744208 74744208 single base substitution G T intron_variant PACA-CA 15 74744208 74744208 single base substitution G T upstream_gene_variant PACA-CA 15 74746480 74746480 single base substitution C T intron_variant PACA-CA 15 74746480 74746480 single base substitution C T upstream_gene_variant PACA-CA 15 74749077 74749077 single base substitution A G intron_variant PACA-CA 15 74749077 74749077 single base substitution A G upstream_gene_variant PACA-CA 15 74753533 74753533 single base substitution C T upstream_gene_variant PACA-CA 15 74756370 74756370 single base substitution A G upstream_gene_variant PAEN-AU 15 74746800 74746800 single base substitution C A intron_variant PAEN-AU 15 74746800 74746800 single base substitution C A upstream_gene_variant PBCA-DE 15 74740755 74740755 single base substitution C A downstream_gene_variant PBCA-DE 15 74740755 74740755 single base substitution C A intron_variant PBCA-DE 15 74749896 74749897 deletion of <=200bp AT - intron_variant PBCA-DE 15 74755467 74755467 single base substitution G T upstream_gene_variant PRAD-CA 15 74736448 74736448 single base substitution T A downstream_gene_variant PRAD-CA 15 74748878 74748878 single base substitution C A intron_variant PRAD-CA 15 74748878 74748878 single base substitution C A upstream_gene_variant PRAD-CA 15 74753376 74753376 single base substitution A G 5_prime_UTR_variant PRAD-CA 15 74753376 74753376 single base substitution A G intron_variant PRAD-CA 15 74753376 74753376 single base substitution A G splice_donor_variant PRAD-UK 15 74738256 74738256 single base substitution G A downstream_gene_variant PRAD-UK 15 74755122 74755122 single base substitution G A upstream_gene_variant RECA-EU 15 74743223 74743223 single base substitution T A intron_variant RECA-EU 15 74743223 74743223 single base substitution T A upstream_gene_variant RECA-EU 15 74753020 74753020 single base substitution G A 5_prime_UTR_variant RECA-EU 15 74753020 74753020 single base substitution G A intron_variant RECA-EU 15 74757937 74757937 single base substitution T A upstream_gene_variant SKCA-BR 15 74741018 74741018 single base substitution A C downstream_gene_variant SKCA-BR 15 74741018 74741018 single base substitution A C intron_variant SKCA-BR 15 74741039 74741039 single base substitution A C downstream_gene_variant SKCA-BR 15 74741039 74741039 single base substitution A C intron_variant SKCA-BR 15 74741064 74741064 single base substitution A C downstream_gene_variant SKCA-BR 15 74741064 74741064 single base substitution A C intron_variant SKCA-BR 15 74743254 74743254 single base substitution G A intron_variant SKCA-BR 15 74743254 74743254 single base substitution G A upstream_gene_variant SKCA-BR 15 74745101 74745101 single base substitution A G intron_variant SKCA-BR 15 74745101 74745101 single base substitution A G upstream_gene_variant SKCA-BR 15 74746565 74746565 single base substitution G A intron_variant SKCA-BR 15 74746565 74746565 single base substitution G A upstream_gene_variant SKCA-BR 15 74747307 74747307 single base substitution C T intron_variant SKCA-BR 15 74747307 74747307 single base substitution C T upstream_gene_variant SKCA-BR 15 74747744 74747744 single base substitution C A intron_variant SKCA-BR 15 74747744 74747744 single base substitution C A upstream_gene_variant SKCA-BR 15 74749867 74749867 single base substitution G A intron_variant SKCA-BR 15 74753514 74753514 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant SKCA-BR 15 74753514 74753514 single base substitution G A upstream_gene_variant SKCA-BR 15 74753522 74753522 single base substitution G A 5_prime_UTR_variant SKCA-BR 15 74753522 74753522 single base substitution G A upstream_gene_variant SKCA-BR 15 74755424 74755425 deletion of <=200bp CT - upstream_gene_variant SKCA-BR 15 74755792 74755792 single base substitution C T upstream_gene_variant SKCM-US 15 74740848 74740848 single base substitution G A downstream_gene_variant SKCM-US 15 74740848 74740848 single base substitution G A intron_variant SKCM-US 15 74740848 74740848 single base substitution G A missense_variant L326F 976C>T SKCM-US 15 74740848 74740848 single base substitution G A missense_variant L60F 178C>T SKCM-US 15 74740913 74740913 single base substitution G A downstream_gene_variant SKCM-US 15 74740913 74740913 single base substitution G A intron_variant SKCM-US 15 74740913 74740913 single base substitution G A missense_variant S304F 911C>T SKCM-US 15 74741550 74741550 single base substitution G A downstream_gene_variant SKCM-US 15 74741550 74741550 single base substitution G A intron_variant SKCM-US 15 74741550 74741550 single base substitution G A missense_variant H287Y 859C>T SKCM-US 15 74741550 74741550 single base substitution G A missense_variant H35Y 103C>T SKCM-US 15 74741678 74741678 single base substitution G A downstream_gene_variant SKCM-US 15 74741678 74741678 single base substitution G A intron_variant SKCM-US 15 74741678 74741678 single base substitution G A missense_variant P188L 563C>T SKCM-US 15 74741678 74741678 single base substitution G A missense_variant P244L 731C>T SKCM-US 15 74741678 74741678 single base substitution G A upstream_gene_variant SKCM-US 15 74742300 74742300 single base substitution G A downstream_gene_variant SKCM-US 15 74742300 74742300 single base substitution G A missense_variant S112F 335C>T SKCM-US 15 74742300 74742300 single base substitution G A missense_variant S158F 473C>T SKCM-US 15 74742300 74742300 single base substitution G A missense_variant S214F 641C>T SKCM-US 15 74742300 74742300 single base substitution G A upstream_gene_variant SKCM-US 15 74742405 74742405 single base substitution A C missense_variant C151G 451T>G SKCM-US 15 74742405 74742405 single base substitution A C missense_variant V123G 368T>G SKCM-US 15 74742405 74742405 single base substitution A C missense_variant V179G 536T>G SKCM-US 15 74742405 74742405 single base substitution A C missense_variant V77G 230T>G SKCM-US 15 74742405 74742405 single base substitution A C upstream_gene_variant SKCM-US 15 74743147 74743147 single base substitution C T missense_variant D120N 358G>A SKCM-US 15 74743147 74743147 single base substitution C T missense_variant D176N 526G>A SKCM-US 15 74743147 74743147 single base substitution C T missense_variant D74N 220G>A SKCM-US 15 74743147 74743147 single base substitution C T synonymous_variant L147L 441G>A SKCM-US 15 74743147 74743147 single base substitution C T upstream_gene_variant SKCM-US 15 74743820 74743820 single base substitution G A intron_variant SKCM-US 15 74743820 74743820 single base substitution G A synonymous_variant I143I 429C>T SKCM-US 15 74743820 74743820 single base substitution G A synonymous_variant I41I 123C>T SKCM-US 15 74743820 74743820 single base substitution G A upstream_gene_variant SKCM-US 15 74751147 74751147 single base substitution G A missense_variant S21F 62C>T STAD-US 15 74741564 74741564 single base substitution G A downstream_gene_variant STAD-US 15 74741564 74741564 single base substitution G A intron_variant STAD-US 15 74741564 74741564 single base substitution G A missense_variant P282L 845C>T STAD-US 15 74741564 74741564 single base substitution G A missense_variant P30L 89C>T STAD-US 15 74749015 74749015 deletion of <=200bp A - splice_region_variant STAD-US 15 74749015 74749015 deletion of <=200bp A - upstream_gene_variant UCEC-US 15 74741579 74741579 single base substitution G A downstream_gene_variant UCEC-US 15 74741579 74741579 single base substitution G A intron_variant UCEC-US 15 74741579 74741579 single base substitution G A missense_variant A221V 662C>T UCEC-US 15 74741579 74741579 single base substitution G A missense_variant A25V 74C>T UCEC-US 15 74741579 74741579 single base substitution G A missense_variant A277V 830C>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand HCC115T COSM1608676 c.61T>C p.S21P Substitution - Missense 15:74458807-74458807 - TCGA-FS-A1ZZ-06 COSM3503933 c.731C>T p.P244L Substitution - Missense 15:74449337-74449337 - T1154 COSM4738761 c.447C>T p.G149G Substitution - coding silent 15:74451461-74451461 - CSCC-35-T COSM4566851 c.492_493CC>TT p.L165F Substitution - Missense 15:74450839-74450840 - TCGA-23-1028-01 COSM78742 c.388G>A p.V130I Substitution - Missense 15:74451520-74451520 - 71 COSM5015314 c.907A>T p.M303L Substitution - Missense 15:74448576-74448576 - Pat_15_B COSM5849765 c.821C>T p.T274I Substitution - Missense 15:74449247-74449247 - PD4836a COSM5798333 c.139A>G p.I47V Substitution - Missense 15:74458729-74458729 - NB-1744 COSM1288802 c.852C>A p.S284R Substitution - Missense 15:74449216-74449216 - ACINAR01 COSM1735313 c.185-3delT p.? Unknown 15:74456674-74456674 - TCGA-A3-3380-01 COSM1493514 c.795G>A p.R265R Substitution - coding silent 15:74449273-74449273 - PT46 COSM5929619 c.390C>T p.V130V Substitution - coding silent 15:74451518-74451518 - TCGA-ER-A195-06 COSM3503934 c.641C>T p.S214F Substitution - Missense 15:74449959-74449959 - LAU618 COSM233700 c.998G>A p.S333N Substitution - Missense 15:74448485-74448485 - SS6003117 COSM5035971 c.665-10C>T p.? Unknown 15:74449685-74449685 - tumor_4166151 COSM5949041 c.1116G>A p.E372E Substitution - coding silent 15:74446117-74446117 - TCGA-BR-6452-01 COSM4056876 c.845C>T p.P282L Substitution - Missense 15:74449223-74449223 - T2269 COSM4738762 c.391T>G p.F131V Substitution - Missense 15:74451517-74451517 - HCC115 COSM1608676 c.61T>C p.S21P Substitution - Missense 15:74458807-74458807 - T3024 COSM4738763 c.71G>A p.R24Q Substitution - Missense 15:74458797-74458797 - BD110T COSM5514293 c.530+5G>A p.? Unknown 15:74450797-74450797 - CSCC-49-T COSM4456688 c.1018C>T p.P340S Substitution - Missense 15:74446215-74446215 - TCGA-EE-A2A1-06 COSM3503935 c.526G>A p.D176N Substitution - Missense 15:74450806-74450806 - SC_9083 COSM5555302 c.988G>C p.G330R Substitution - Missense 15:74448495-74448495 - TCGA-B0-5088-01 COSM471053 c.275A>G p.K92R Substitution - Missense 15:74456581-74456581 - S00827 COSM316332 c.963C>A p.A321A Substitution - coding silent 15:74448520-74448520 - TCGA-DU-5852-01 COSM3969272 c.141T>C p.I47I Substitution - coding silent 15:74458727-74458727 - 4 COSM5732145 c.340C>T p.R114W Substitution - Missense 15:74452343-74452343 - ESO-120 COSM1269644 c.724T>A p.S242T Substitution - Missense 15:74449344-74449344 - TCGA-EE-A2GJ-06 COSM3503934 c.641C>T p.S214F Substitution - Missense 15:74449959-74449959 - CHC1741T COSM4805546 c.24G>A p.L8L Substitution - coding silent 15:74458844-74458844 - PD4267a COSM5794538 c.180G>C p.L60L Substitution - coding silent 15:74458688-74458688 - SNU-175 COSM1938546 c.889T>C p.S297P Substitution - Missense 15:74448594-74448594 - LC_C4 COSM1189062 c.59A>C p.K20T Substitution - Missense 15:74458809-74458809 - TCGA-BR-6566-01 COSM4056876 c.845C>T p.P282L Substitution - Missense 15:74449223-74449223 - pfg122T COSM4757572 c.1091G>A p.G364D Substitution - Missense 15:74446142-74446142 - TCGA-G4-6628-01 COSM1374535 c.754C>T p.R252C Substitution - Missense 15:74449314-74449314 - ATL001 COSM1938575 c.26C>T p.A9V Substitution - Missense 15:74458842-74458842 - TCGA-ER-A3PL-06 COSM3503937 c.62C>T p.S21F Substitution - Missense 15:74458806-74458806 - PCSI_0090_Pa_X COSM3377658 c.1073G>A p.R358Q Substitution - Missense 15:74446160-74446160 - YUGURT COSM5383824 c.602C>T p.P201L Substitution - Missense 15:74449998-74449998 - CSCC-16-T COSM3503934 c.641C>T p.S214F Substitution - Missense 15:74449959-74449959 - TCGA-ER-A19F-06 COSM3503936 c.429C>T p.I143I Substitution - coding silent 15:74451479-74451479 - RKO COSM4647849 c.358C>A p.L120M Substitution - Missense 15:74452325-74452325 - PT53 COSM5941382 c.1005+7C>T p.? Unknown 15:74448471-74448471 - CSCC-17-T COSM4535053 c.214G>A p.D72N Substitution - Missense 15:74456642-74456642 - TCGA-22-5473-01 COSM701206 c.1102C>T p.Q368* Substitution - Nonsense 15:74446131-74446131 - PT42 COSM5925842 c.902C>T p.S301L Substitution - Missense 15:74448581-74448581 - CLL105 COSM1290430 c.944A>G p.N315S Substitution - Missense 15:74448539-74448539 - S00827 COSM316332 c.963C>A p.A321A Substitution - coding silent 15:74448520-74448520 - TCGA-AC-A3W6-01 COSM3816732 c.807G>C p.Q269H Substitution - Missense 15:74449261-74449261 - LUAD-S01409 COSM346434 c.27G>C p.A9A Substitution - coding silent 15:74458841-74458841 - TCGA-D1-A17F-01 COSM964839 c.830C>T p.A277V Substitution - Missense 15:74449238-74449238 - TCGA-CM-6169-01 COSM1374533 c.1017_1018insG p.P340fs*8 Insertion - Frameshift 15:74446215-74446216 - TCGA-22-5477-01 COSM701205 c.123A>T p.S41S Substitution - coding silent 15:74458745-74458745 - HCC159T COSM3706730 c.446G>A p.G149D Substitution - Missense 15:74451462-74451462 - TCGA-D3-A5GO-06 COSM3887497 c.536T>G p.V179G Substitution - Missense 15:74450064-74450064 - LUAD-RT-S01774 COSM381411 c.1045G>A p.G349S Substitution - Missense 15:74446188-74446188 - pfg344T COSM4757573 c.893C>A p.S298* Substitution - Nonsense 15:74448590-74448590 - TCGA-DK-A3X1-01 COSM3794397 c.192C>A p.I64I Substitution - coding silent 15:74456664-74456664 - CHC1741T COSM4805546 c.24G>A p.L8L Substitution - coding silent 15:74458844-74458844 - 111097 COSM1645103 c.748A>G p.S250G Substitution - Missense 15:74449320-74449320 - TCGA-AY-6197-01 COSM1374537 c.129G>A p.L43L Substitution - coding silent 15:74458739-74458739 - HCC105T COSM5818466 c.92G>C p.G31A Substitution - Missense 15:74458776-74458776 - TCGA-FW-A3R5-06 COSM3887495 c.911C>T p.S304F Substitution - Missense 15:74448572-74448572 - CSCC-16-T COSM4456444 c.1009C>T p.Q337* Substitution - Nonsense 15:74446224-74446224 - BD57T COSM5510744 c.822C>T p.T274T Substitution - coding silent 15:74449246-74449246 - SNU-175 COSM1938554 c.586G>A p.V196I Substitution - Missense 15:74450014-74450014 - TCGA-ER-A19E-06 COSM3503932 c.976C>T p.L326F Substitution - Missense 15:74448507-74448507 - TCGA-DK-A3X1-01 COSM3794398 c.11C>T p.S4L Substitution - Missense 15:74458857-74458857 - TCGA-CK-4950-01 COSM1374534 c.982G>A p.A328T Substitution - Missense 15:74448501-74448501 - HT55 COSM1938567 c.199G>A p.G67S Substitution - Missense 15:74456657-74456657 - HCC159 COSM3706730 c.446G>A p.G149D Substitution - Missense 15:74451462-74451462 - TCGA-QB-A6FS-06 COSM3887496 c.859C>T p.H287Y Substitution - Missense 15:74449209-74449209 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.334713 15q24.1 609748 2421680|CGAP|BC007913|C/T|coding|Val87Val|724|Candidate; 2421680|CGAP|BC030055|C/T|coding|Val87Val|418|Candidate; 2421680|CGAP|BC033919|C/T|coding|Val87Val|459|Candidate

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G Missense p.I155T c.464T>C 15 74743785 BRCA A G Synonymous p.I47I c.141T>C 15 74751068 LGG A T Missense p.S242T c.724T>A 15 74741685 ESCA C T Missense p.D176N c.526G>A 15 74743147 CM C T Missense p.V130I c.388G>A 15 74743861 OV C T Synonymous p.Q323Q c.969G>A 15 74740855 HNSC G A Missense p.A277V c.830C>T 15 74741579 UCEC G A Missense p.L326F c.976C>T 15 74740848 CM G A Missense p.P244L c.731C>T 15 74741678 CM G A Missense p.S209F c.626C>T 15 74742315 CM G A Missense p.S214F c.641C>T 15 74742300 CM G A Nonsense p.Q368* c.1102C>T 15 74738472 LUSC G A Synonymous p.D347D c.1041C>T 15 74738533 HNSC G A Synonymous p.I143I c.429C>T 15 74743820 CM G T Missense p.S284R c.852C>A 15 74741557 NB G T Synonymous p.A321A c.963C>A 15 74740861 SCLC T A Missense p.Q368L c.1103A>T 15 74738471 CM T A Synonymous p.S41S c.123A>T 15 74751086 LUSC T C Missense p.N315S c.944A>G 15 74740880 CLL