Mutation - TCGA Type Chromosome Start Position End Position Strand Variant Classification Variant Type Reference Allele Tumor_seq Allele 1 Tumor_seq Allele 2 Tumor Sample Barcode Matched Norm Sample Barcode Genome Change cDNA Change Codon Change Protein Change ACC 17 1359363 1359363 + Silent SNP T T G TCGA-OR-A5KU-01A-11D-A29I-10 TCGA-OR-A5KU-10A-01D-A29L-10 g.chr17:1359363T>G c.49A>C c.(49-51)Agg>Cgg p.R17R BLCA 17 1340222 1340222 + Missense_Mutation SNP C C T TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr17:1340222C>T c.469G>A c.(469-471)Gac>Aac p.D157N BLCA 17 1340249 1340249 + Missense_Mutation SNP C C G TCGA-XF-A9SL-01A-11D-A391-08 TCGA-XF-A9SL-10A-01D-A394-08 g.chr17:1340249C>G c.442G>C c.(442-444)Gag>Cag p.E148Q BLCA 17 1340297 1340297 + Missense_Mutation SNP C C G TCGA-FD-A6TC-01A-21D-A339-08 TCGA-FD-A6TC-10A-21D-A339-08 g.chr17:1340297C>G c.394G>C c.(394-396)Gag>Cag p.E132Q BLCA 17 1340408 1340408 + Missense_Mutation SNP C C G TCGA-MV-A51V-01A-11D-A26M-08 TCGA-MV-A51V-10A-01D-A26K-08 g.chr17:1340408C>G c.283G>C c.(283-285)Gat>Cat p.D95H BLCA 17 1359265 1359265 + Silent SNP G G A TCGA-E7-A678-01A-11D-A30E-08 TCGA-E7-A678-10A-01D-A30H-08 g.chr17:1359265G>A c.147C>T c.(145-147)ctC>ctT p.L49L BRCA 17 1340206 1340206 + Missense_Mutation SNP C C T TCGA-AR-A24X-01A-11D-A167-09 TCGA-AR-A24X-10A-01D-A167-09 g.chr17:1340206C>T c.485G>A c.(484-486)cGg>cAg p.R162Q CESC 17 1326941 1326941 + Missense_Mutation SNP C C T TCGA-C5-A7CL-01A-11D-A32I-09 TCGA-C5-A7CL-10A-01D-A32I-09 g.chr17:1326941C>T c.781G>A c.(781-783)Ggt>Agt p.G261S COAD 17 1340133 1340133 + Silent SNP G G A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr17:1340133G>A c.558C>T c.(556-558)taC>taT p.Y186Y COADREAD 17 1340133 1340133 + Silent SNP G G A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr17:1340133G>A c.558C>T c.(556-558)taC>taT p.Y186Y ESCA 17 1340045 1340045 + Missense_Mutation SNP G G T TCGA-IC-A6RF-01A-13D-A33E-09 TCGA-IC-A6RF-10A-21D-A33H-09 g.chr17:1340045G>T c.646C>A c.(646-648)Ccg>Acg p.P216T HNSC 17 1340132 1340132 + Missense_Mutation SNP C C T TCGA-CN-5365-01A-01D-1434-08 TCGA-CN-5365-10A-01D-1434-08 g.chr17:1340132C>T c.559G>A c.(559-561)Gtc>Atc p.V187I HNSC 17 1340185 1340185 + Nonsense_Mutation SNP C C T TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr17:1340185C>T c.506G>A c.(505-507)tGg>tAg p.W169* KIPAN 17 1326915 1326915 + Silent SNP A A G TCGA-B0-5107-01A-01D-1421-08 TCGA-B0-5107-11A-01D-1421-08 g.chr17:1326915A>G c.807T>C c.(805-807)atT>atC p.I269I KIRC 17 1326915 1326915 + Silent SNP A A G TCGA-B0-5107-01A-01D-1421-08 TCGA-B0-5107-11A-01D-1421-08 g.chr17:1326915A>G c.807T>C c.(805-807)atT>atC p.I269I LIHC 17 1359301 1359301 + Silent SNP C C T TCGA-DD-AADP-01A-11D-A38X-10 TCGA-DD-AADP-10A-01D-A38X-10 g.chr17:1359301C>T c.111G>A c.(109-111)gtG>gtA p.V37V LUAD 17 1326904 1326904 + Frame_Shift_Del DEL C C - TCGA-55-7725-01A-11D-2167-08 TCGA-55-7725-10A-01D-2167-08 g.chr17:1326904delC c.818delG c.(817-819)ggtfs p.G273fs LUAD 17 1359352 1359352 + Silent SNP C C A TCGA-62-8394-01A-11D-2323-08 TCGA-62-8394-10A-01D-2323-08 g.chr17:1359352C>A c.60G>T c.(58-60)cgG>cgT p.R20R PAAD 17 1340290 1340290 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr17:1340290G>A c.401C>T c.(400-402)gCg>gTg p.A134V PRAD 17 1339932 1339932 + Silent SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr17:1339932C>T c.759G>A c.(757-759)aaG>aaA p.K253K PRAD 17 1340400 1340400 + Silent SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr17:1340400C>T c.291G>A c.(289-291)ttG>ttA p.L97L PRAD 17 1359240 1359240 + Missense_Mutation SNP A A C TCGA-CH-5748-01A-11D-1576-08 TCGA-CH-5748-10A-01D-1576-08 g.chr17:1359240A>C c.172T>G c.(172-174)Tcc>Gcc p.S58A SKCM 17 1339973 1339973 + Missense_Mutation SNP C C A TCGA-GF-A6C8-06A-12D-A30X-08 TCGA-GF-A6C8-10A-01D-A30X-08 g.chr17:1339973C>A c.718G>T c.(718-720)Gcc>Tcc p.A240S SKCM 17 1340197 1340197 + Missense_Mutation SNP G G A TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr17:1340197G>A c.494C>T c.(493-495)cCt>cTt p.P165L SKCM 17 1340235 1340235 + Silent SNP G G C TCGA-DA-A1HV-06A-21D-A196-08 TCGA-DA-A1HV-10A-01D-A198-08 g.chr17:1340235G>C c.456C>G c.(454-456)ccC>ccG p.P152P SKCM 17 1340260 1340260 + Missense_Mutation SNP T T A TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr17:1340260T>A c.431A>T c.(430-432)aAt>aTt p.N144I

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 17 1370776 1370776 single base substitution G A upstream_gene_variant BLCA-US 17 1371362 1371362 single base substitution T C upstream_gene_variant BRCA-EU 17 1319079 1319079 single base substitution C T downstream_gene_variant BRCA-EU 17 1320177 1320177 single base substitution G A downstream_gene_variant BRCA-EU 17 1321909 1321909 single base substitution C G downstream_gene_variant BRCA-EU 17 1322651 1322651 single base substitution T C downstream_gene_variant BRCA-EU 17 1324378 1324378 deletion of <=200bp T - 3_prime_UTR_variant BRCA-EU 17 1324378 1324378 deletion of <=200bp T - downstream_gene_variant BRCA-EU 17 1328315 1328315 deletion of <=200bp A - intron_variant BRCA-EU 17 1329260 1329260 single base substitution G A intron_variant BRCA-EU 17 1329357 1329357 single base substitution C T intron_variant BRCA-EU 17 1331635 1331635 single base substitution T A intron_variant BRCA-EU 17 1332552 1332552 single base substitution G A intron_variant BRCA-EU 17 1333835 1333835 single base substitution T G intron_variant BRCA-EU 17 1335434 1335434 single base substitution C A intron_variant BRCA-EU 17 1336579 1336579 single base substitution C A intron_variant BRCA-EU 17 1339287 1339287 single base substitution G C intron_variant BRCA-EU 17 1340008 1340008 single base substitution G A intron_variant BRCA-EU 17 1340008 1340008 single base substitution G A missense_variant T228I 683C>T BRCA-EU 17 1342093 1342093 single base substitution C G intron_variant BRCA-EU 17 1342140 1342140 single base substitution T A intron_variant BRCA-EU 17 1342636 1342636 single base substitution C T intron_variant BRCA-EU 17 1344758 1344758 single base substitution G C intron_variant BRCA-EU 17 1346958 1346958 single base substitution G A intron_variant BRCA-EU 17 1347584 1347584 single base substitution C T intron_variant BRCA-EU 17 1352974 1352974 deletion of <=200bp A - intron_variant BRCA-EU 17 1355014 1355014 deletion of <=200bp A - intron_variant BRCA-EU 17 1357899 1357899 single base substitution T G intron_variant BRCA-EU 17 1358051 1358051 single base substitution A T intron_variant BRCA-EU 17 1358659 1358659 single base substitution G A intron_variant BRCA-EU 17 1359095 1359095 single base substitution C T intron_variant BRCA-EU 17 1363752 1363752 single base substitution C G intron_variant BRCA-EU 17 1363752 1363752 single base substitution C G upstream_gene_variant BRCA-EU 17 1364242 1364242 single base substitution A C intron_variant BRCA-EU 17 1364242 1364242 single base substitution A C upstream_gene_variant BRCA-EU 17 1366512 1366512 single base substitution G C upstream_gene_variant BRCA-EU 17 1366920 1366920 single base substitution G T upstream_gene_variant BRCA-EU 17 1368103 1368103 single base substitution G T upstream_gene_variant BRCA-EU 17 1368685 1368685 single base substitution T A upstream_gene_variant BRCA-EU 17 1368686 1368686 single base substitution A T upstream_gene_variant BRCA-EU 17 1369920 1369920 single base substitution C G upstream_gene_variant BRCA-FR 17 1319079 1319079 single base substitution C T downstream_gene_variant BRCA-FR 17 1322855 1322855 single base substitution C G downstream_gene_variant BRCA-FR 17 1325800 1325800 single base substitution G A 3_prime_UTR_variant BRCA-FR 17 1325800 1325800 single base substitution G A downstream_gene_variant BRCA-FR 17 1331834 1331834 single base substitution T C intron_variant BRCA-FR 17 1332552 1332552 single base substitution G A intron_variant BRCA-FR 17 1340008 1340008 single base substitution G A intron_variant BRCA-FR 17 1340008 1340008 single base substitution G A missense_variant T228I 683C>T BRCA-FR 17 1363471 1363471 single base substitution G T intron_variant BRCA-FR 17 1363471 1363471 single base substitution G T upstream_gene_variant BRCA-FR 17 1365071 1365071 single base substitution A T intron_variant BRCA-FR 17 1368686 1368686 single base substitution A T upstream_gene_variant BRCA-KR 17 1326773 1326773 single base substitution G T 3_prime_UTR_variant BRCA-KR 17 1326773 1326773 single base substitution G T exon_variant BRCA-KR 17 1326773 1326773 single base substitution G T intron_variant BRCA-US 17 1340206 1340206 single base substitution C T exon_variant BRCA-US 17 1340206 1340206 single base substitution C T intron_variant BRCA-US 17 1340206 1340206 single base substitution C T missense_variant R162Q 485G>A BTCA-JP 17 1368993 1368993 single base substitution G A upstream_gene_variant BTCA-JP 17 1371154 1371154 single base substitution G A upstream_gene_variant CESC-US 17 1326754 1326754 insertion of <=200bp - A 3_prime_UTR_variant CESC-US 17 1326754 1326754 insertion of <=200bp - A exon_variant CESC-US 17 1326754 1326754 insertion of <=200bp - A intron_variant CESC-US 17 1326941 1326941 single base substitution C T exon_variant CESC-US 17 1326941 1326941 single base substitution C T intron_variant CESC-US 17 1326941 1326941 single base substitution C T missense_variant G261S 781G>A CESC-US 17 1326941 1326941 single base substitution C T missense_variant R204Q 611G>A CESC-US 17 1370785 1370785 single base substitution G A upstream_gene_variant CESC-US 17 1371352 1371352 single base substitution G C upstream_gene_variant CLLE-ES 17 1349477 1349477 single base substitution G C intron_variant CLLE-ES 17 1359123 1359123 single base substitution C G intron_variant COAD-US 17 1359363 1359363 single base substitution T G intron_variant COAD-US 17 1359363 1359363 single base substitution T G synonymous_variant R17R 49A>C COAD-US 17 1369024 1369024 single base substitution C A upstream_gene_variant COCA-CN 17 1326755 1326755 single base substitution A G 3_prime_UTR_variant COCA-CN 17 1326755 1326755 single base substitution A G exon_variant COCA-CN 17 1326755 1326755 single base substitution A G intron_variant COCA-CN 17 1326965 1326965 single base substitution G C intron_variant COCA-CN 17 1370966 1370966 single base substitution C T upstream_gene_variant COCA-CN 17 1371150 1371150 single base substitution G A upstream_gene_variant EOPC-DE 17 1363085 1363085 single base substitution G A intron_variant EOPC-DE 17 1363085 1363085 single base substitution G A upstream_gene_variant ESAD-UK 17 1319199 1319199 single base substitution C T downstream_gene_variant ESAD-UK 17 1321415 1321415 single base substitution T G downstream_gene_variant ESAD-UK 17 1323446 1323446 single base substitution C A downstream_gene_variant ESAD-UK 17 1324378 1324378 deletion of <=200bp T - 3_prime_UTR_variant ESAD-UK 17 1324378 1324378 deletion of <=200bp T - downstream_gene_variant ESAD-UK 17 1325617 1325617 single base substitution C T 3_prime_UTR_variant ESAD-UK 17 1325617 1325617 single base substitution C T downstream_gene_variant ESAD-UK 17 1325738 1325738 single base substitution T G 3_prime_UTR_variant ESAD-UK 17 1325738 1325738 single base substitution T G downstream_gene_variant ESAD-UK 17 1326508 1326508 single base substitution G A 3_prime_UTR_variant ESAD-UK 17 1326508 1326508 single base substitution G A downstream_gene_variant ESAD-UK 17 1326508 1326508 single base substitution G A intron_variant ESAD-UK 17 1327299 1327299 insertion of <=200bp - CTCACTACCC intron_variant ESAD-UK 17 1331123 1331123 single base substitution C G intron_variant ESAD-UK 17 1333297 1333297 single base substitution A G intron_variant ESAD-UK 17 1334638 1334638 single base substitution C T intron_variant ESAD-UK 17 1335654 1335654 single base substitution A G intron_variant ESAD-UK 17 1341578 1341578 single base substitution C T intron_variant ESAD-UK 17 1342593 1342593 single base substitution G A intron_variant ESAD-UK 17 1344514 1344514 single base substitution G A intron_variant ESAD-UK 17 1349869 1349869 single base substitution C A intron_variant ESAD-UK 17 1351355 1351355 single base substitution G C intron_variant ESAD-UK 17 1353601 1353601 single base substitution G A intron_variant ESAD-UK 17 1354723 1354723 single base substitution A T intron_variant ESAD-UK 17 1355188 1355188 single base substitution A T intron_variant ESAD-UK 17 1355680 1355680 single base substitution A G intron_variant ESAD-UK 17 1362393 1362393 single base substitution G A intron_variant ESAD-UK 17 1362393 1362393 single base substitution G A upstream_gene_variant ESAD-UK 17 1362554 1362554 single base substitution G A intron_variant ESAD-UK 17 1362554 1362554 single base substitution G A upstream_gene_variant ESAD-UK 17 1363551 1363551 single base substitution T G intron_variant ESAD-UK 17 1363551 1363551 single base substitution T G upstream_gene_variant ESAD-UK 17 1363826 1363826 deletion of <=200bp T - intron_variant ESAD-UK 17 1363826 1363826 deletion of <=200bp T - upstream_gene_variant ESAD-UK 17 1366619 1366619 single base substitution G A upstream_gene_variant ESCA-CN 17 1370459 1370459 single base substitution T C upstream_gene_variant KIRC-US 17 1326915 1326915 single base substitution A G 3_prime_UTR_variant KIRC-US 17 1326915 1326915 single base substitution A G exon_variant KIRC-US 17 1326915 1326915 single base substitution A G intron_variant KIRC-US 17 1326915 1326915 single base substitution A G synonymous_variant I269I 807T>C KIRP-US 17 1370772 1370772 single base substitution A C upstream_gene_variant LAML-KR 17 1322443 1322443 single base substitution C T downstream_gene_variant LICA-FR 17 1320902 1320902 single base substitution T C downstream_gene_variant LICA-FR 17 1322927 1322928 deletion of <=200bp TT - downstream_gene_variant LICA-FR 17 1323746 1323746 single base substitution G A downstream_gene_variant LICA-FR 17 1345537 1345537 single base substitution T G intron_variant LICA-FR 17 1350902 1350902 deletion of <=200bp T - intron_variant LICA-FR 17 1358307 1358307 single base substitution A G intron_variant LINC-JP 17 1319963 1319963 single base substitution C G downstream_gene_variant LINC-JP 17 1325962 1325962 single base substitution T C 3_prime_UTR_variant LINC-JP 17 1325962 1325962 single base substitution T C downstream_gene_variant LINC-JP 17 1327010 1327010 single base substitution C A intron_variant LINC-JP 17 1342642 1342642 single base substitution C A intron_variant LINC-JP 17 1351760 1351760 single base substitution T A intron_variant LINC-JP 17 1354506 1354506 single base substitution G A intron_variant LINC-JP 17 1359406 1359406 single base substitution C T intron_variant LINC-JP 17 1359406 1359406 single base substitution C T synonymous_variant A2A 6G>A LIRI-JP 17 1320390 1320390 single base substitution C T downstream_gene_variant LIRI-JP 17 1324872 1324872 single base substitution T C 3_prime_UTR_variant LIRI-JP 17 1324872 1324872 single base substitution T C downstream_gene_variant LIRI-JP 17 1326878 1326878 single base substitution T C 3_prime_UTR_variant LIRI-JP 17 1326878 1326878 single base substitution T C exon_variant LIRI-JP 17 1326878 1326878 single base substitution T C intron_variant LIRI-JP 17 1326878 1326878 single base substitution T C missense_variant K282E 844A>G LIRI-JP 17 1327577 1327577 single base substitution T C intron_variant LIRI-JP 17 1327672 1327672 single base substitution T G intron_variant LIRI-JP 17 1328138 1328138 single base substitution T C intron_variant LIRI-JP 17 1329041 1329041 single base substitution A T intron_variant LIRI-JP 17 1335102 1335102 single base substitution A G intron_variant LIRI-JP 17 1336876 1336876 single base substitution G T intron_variant LIRI-JP 17 1338282 1338282 single base substitution G C intron_variant LIRI-JP 17 1342103 1342103 single base substitution C A intron_variant LIRI-JP 17 1344286 1344286 single base substitution G T intron_variant LIRI-JP 17 1351878 1351878 single base substitution T C intron_variant LIRI-JP 17 1355545 1355545 single base substitution T C intron_variant LIRI-JP 17 1355675 1355675 single base substitution T C intron_variant LIRI-JP 17 1356891 1356891 single base substitution T C intron_variant LIRI-JP 17 1357898 1357898 single base substitution T A intron_variant LIRI-JP 17 1365567 1365567 single base substitution T C intron_variant LIRI-JP 17 1368782 1368782 single base substitution C A upstream_gene_variant LUSC-KR 17 1322568 1322568 single base substitution A T downstream_gene_variant LUSC-KR 17 1325743 1325743 single base substitution C T 3_prime_UTR_variant LUSC-KR 17 1325743 1325743 single base substitution C T downstream_gene_variant LUSC-KR 17 1336070 1336070 single base substitution C A intron_variant LUSC-KR 17 1338894 1338894 single base substitution C T intron_variant LUSC-KR 17 1341190 1341190 single base substitution T C intron_variant LUSC-KR 17 1343421 1343421 single base substitution G A intron_variant LUSC-KR 17 1353467 1353467 single base substitution C A intron_variant LUSC-KR 17 1358915 1358915 single base substitution C G intron_variant LUSC-KR 17 1360581 1360581 single base substitution G T intron_variant LUSC-KR 17 1360581 1360581 single base substitution G T upstream_gene_variant LUSC-KR 17 1364219 1364219 single base substitution C G intron_variant LUSC-KR 17 1364219 1364219 single base substitution C G upstream_gene_variant LUSC-KR 17 1371123 1371123 single base substitution T C upstream_gene_variant LUSC-KR 17 1371393 1371393 single base substitution C T upstream_gene_variant MALY-DE 17 1330932 1330932 single base substitution T G intron_variant MALY-DE 17 1331839 1331839 single base substitution A G intron_variant MALY-DE 17 1335368 1335368 single base substitution C G intron_variant MALY-DE 17 1336393 1336393 single base substitution A G intron_variant MALY-DE 17 1337432 1337432 single base substitution T C intron_variant MALY-DE 17 1337708 1337708 single base substitution T A intron_variant MALY-DE 17 1347296 1347296 deletion of <=200bp T - intron_variant MALY-DE 17 1358639 1358639 single base substitution A G intron_variant MALY-DE 17 1362234 1362234 single base substitution T G intron_variant MALY-DE 17 1362234 1362234 single base substitution T G upstream_gene_variant MALY-DE 17 1362601 1362601 single base substitution G T intron_variant MALY-DE 17 1362601 1362601 single base substitution G T upstream_gene_variant MELA-AU 17 1319893 1319893 single base substitution G A downstream_gene_variant MELA-AU 17 1319995 1319995 single base substitution G A downstream_gene_variant MELA-AU 17 1320551 1320552 multiple base substitution (>=2bp and <=200bp) AA CT downstream_gene_variant MELA-AU 17 1321533 1321533 single base substitution C T downstream_gene_variant MELA-AU 17 1321953 1321953 single base substitution G A downstream_gene_variant MELA-AU 17 1322216 1322216 single base substitution G A downstream_gene_variant MELA-AU 17 1322648 1322648 single base substitution G A downstream_gene_variant MELA-AU 17 1322914 1322914 single base substitution G A downstream_gene_variant MELA-AU 17 1322918 1322918 single base substitution A G downstream_gene_variant MELA-AU 17 1323498 1323498 single base substitution G A downstream_gene_variant MELA-AU 17 1323499 1323499 single base substitution G A downstream_gene_variant MELA-AU 17 1323766 1323766 single base substitution T C downstream_gene_variant MELA-AU 17 1323957 1323957 single base substitution G A downstream_gene_variant MELA-AU 17 1324502 1324503 multiple base substitution (>=2bp and <=200bp) CC TT 3_prime_UTR_variant MELA-AU 17 1324502 1324503 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 17 1324586 1324586 single base substitution G A 3_prime_UTR_variant MELA-AU 17 1324586 1324586 single base substitution G A downstream_gene_variant MELA-AU 17 1325142 1325142 single base substitution G A 3_prime_UTR_variant MELA-AU 17 1325142 1325142 single base substitution G A downstream_gene_variant MELA-AU 17 1325357 1325357 single base substitution G C 3_prime_UTR_variant MELA-AU 17 1325357 1325357 single base substitution G C downstream_gene_variant MELA-AU 17 1326994 1326994 single base substitution G A intron_variant MELA-AU 17 1327360 1327360 single base substitution C T intron_variant MELA-AU 17 1327815 1327815 single base substitution G A intron_variant MELA-AU 17 1328023 1328023 single base substitution G A intron_variant MELA-AU 17 1328237 1328238 multiple base substitution (>=2bp and <=200bp) GG TA intron_variant MELA-AU 17 1328350 1328350 single base substitution A T intron_variant MELA-AU 17 1329963 1329963 single base substitution G A intron_variant MELA-AU 17 1331777 1331777 single base substitution G A intron_variant MELA-AU 17 1332098 1332098 single base substitution G A intron_variant MELA-AU 17 1332282 1332282 single base substitution G A intron_variant MELA-AU 17 1332469 1332469 single base substitution G A intron_variant MELA-AU 17 1332875 1332876 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 17 1333354 1333354 single base substitution T A intron_variant MELA-AU 17 1334270 1334270 single base substitution G A intron_variant MELA-AU 17 1334592 1334592 single base substitution G A intron_variant MELA-AU 17 1334960 1334960 single base substitution C T intron_variant MELA-AU 17 1335143 1335143 single base substitution A G intron_variant MELA-AU 17 1335459 1335459 single base substitution T C intron_variant MELA-AU 17 1335604 1335604 single base substitution G A intron_variant MELA-AU 17 1338598 1338599 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 17 1339866 1339866 single base substitution G A intron_variant MELA-AU 17 1340130 1340130 single base substitution G A exon_variant MELA-AU 17 1340130 1340130 single base substitution G A intron_variant MELA-AU 17 1340130 1340130 single base substitution G A synonymous_variant V187V 561C>T MELA-AU 17 1340207 1340207 single base substitution G A exon_variant MELA-AU 17 1340207 1340207 single base substitution G A intron_variant MELA-AU 17 1340207 1340207 single base substitution G A missense_variant R162W 484C>T MELA-AU 17 1340867 1340867 single base substitution G A intron_variant MELA-AU 17 1341961 1341961 single base substitution G A intron_variant MELA-AU 17 1342363 1342363 single base substitution G A intron_variant MELA-AU 17 1342606 1342606 single base substitution T A intron_variant MELA-AU 17 1343159 1343159 single base substitution G A intron_variant MELA-AU 17 1343487 1343488 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 17 1343488 1343488 single base substitution G A intron_variant MELA-AU 17 1344572 1344572 single base substitution T C intron_variant MELA-AU 17 1346208 1346208 single base substitution G A intron_variant MELA-AU 17 1348019 1348019 single base substitution T A intron_variant MELA-AU 17 1348103 1348103 single base substitution G A intron_variant MELA-AU 17 1348153 1348153 single base substitution G A intron_variant MELA-AU 17 1348538 1348538 single base substitution G A intron_variant MELA-AU 17 1348630 1348630 single base substitution A G intron_variant MELA-AU 17 1348830 1348830 single base substitution A C intron_variant MELA-AU 17 1348976 1348976 single base substitution G A intron_variant MELA-AU 17 1349577 1349577 single base substitution G A intron_variant MELA-AU 17 1351616 1351616 single base substitution A G intron_variant MELA-AU 17 1352810 1352810 single base substitution G A intron_variant MELA-AU 17 1353475 1353475 single base substitution G A intron_variant MELA-AU 17 1353793 1353793 single base substitution G A intron_variant MELA-AU 17 1354125 1354125 single base substitution A G intron_variant MELA-AU 17 1354415 1354415 single base substitution G A intron_variant MELA-AU 17 1355174 1355174 single base substitution G A intron_variant MELA-AU 17 1356196 1356196 single base substitution G A intron_variant MELA-AU 17 1356284 1356285 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 17 1356961 1356961 single base substitution G A intron_variant MELA-AU 17 1357668 1357668 single base substitution C T intron_variant MELA-AU 17 1357672 1357672 single base substitution G A intron_variant MELA-AU 17 1359236 1359236 single base substitution T C intron_variant MELA-AU 17 1359236 1359236 single base substitution T C missense_variant H59R 176A>G MELA-AU 17 1359397 1359397 single base substitution G A intron_variant MELA-AU 17 1359397 1359397 single base substitution G A synonymous_variant F5F 15C>T MELA-AU 17 1359624 1359624 single base substitution G A intron_variant MELA-AU 17 1359624 1359624 single base substitution G A upstream_gene_variant MELA-AU 17 1359700 1359700 single base substitution G A intron_variant MELA-AU 17 1359700 1359700 single base substitution G A upstream_gene_variant MELA-AU 17 1359706 1359706 single base substitution G A intron_variant MELA-AU 17 1359706 1359706 single base substitution G A upstream_gene_variant MELA-AU 17 1359856 1359856 single base substitution G T intron_variant MELA-AU 17 1359856 1359856 single base substitution G T upstream_gene_variant MELA-AU 17 1359874 1359874 single base substitution C T intron_variant MELA-AU 17 1359874 1359874 single base substitution C T upstream_gene_variant MELA-AU 17 1360501 1360501 single base substitution C T intron_variant MELA-AU 17 1360501 1360501 single base substitution C T upstream_gene_variant MELA-AU 17 1363532 1363532 single base substitution G A intron_variant MELA-AU 17 1363532 1363532 single base substitution G A upstream_gene_variant MELA-AU 17 1363639 1363639 single base substitution G A intron_variant MELA-AU 17 1363639 1363639 single base substitution G A upstream_gene_variant MELA-AU 17 1363929 1363929 single base substitution G A intron_variant MELA-AU 17 1363929 1363929 single base substitution G A upstream_gene_variant MELA-AU 17 1364136 1364136 single base substitution G A intron_variant MELA-AU 17 1364136 1364136 single base substitution G A upstream_gene_variant MELA-AU 17 1364343 1364343 single base substitution G A intron_variant MELA-AU 17 1364343 1364343 single base substitution G A upstream_gene_variant MELA-AU 17 1364345 1364345 single base substitution G A intron_variant MELA-AU 17 1364345 1364345 single base substitution G A upstream_gene_variant MELA-AU 17 1366264 1366264 single base substitution G A exon_variant MELA-AU 17 1366410 1366410 single base substitution G A exon_variant MELA-AU 17 1366840 1366840 single base substitution C T upstream_gene_variant MELA-AU 17 1367036 1367036 single base substitution G A upstream_gene_variant MELA-AU 17 1367223 1367223 single base substitution G A upstream_gene_variant MELA-AU 17 1367599 1367599 single base substitution G A upstream_gene_variant MELA-AU 17 1367681 1367681 single base substitution G A upstream_gene_variant MELA-AU 17 1368828 1368829 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 17 1368829 1368829 single base substitution G A upstream_gene_variant MELA-AU 17 1369786 1369786 single base substitution G A upstream_gene_variant MELA-AU 17 1370518 1370518 single base substitution A T upstream_gene_variant ORCA-IN 17 1351936 1351937 deletion of <=200bp AG - intron_variant ORCA-IN 17 1364552 1364552 single base substitution G A intron_variant ORCA-IN 17 1364552 1364552 single base substitution G A upstream_gene_variant ORCA-IN 17 1369243 1369243 single base substitution G C upstream_gene_variant ORCA-IN 17 1371382 1371382 single base substitution G T upstream_gene_variant OV-AU 17 1337316 1337316 single base substitution C A intron_variant OV-AU 17 1343981 1343981 single base substitution T G intron_variant OV-AU 17 1346815 1346815 single base substitution A C intron_variant OV-AU 17 1346845 1346845 single base substitution A G intron_variant OV-AU 17 1354455 1354455 single base substitution C A intron_variant OV-AU 17 1356244 1356244 single base substitution T C intron_variant OV-AU 17 1357139 1357139 single base substitution T C intron_variant OV-AU 17 1367338 1367338 single base substitution G C upstream_gene_variant OV-AU 17 1368352 1368352 single base substitution C T upstream_gene_variant PACA-AU 17 1321545 1321545 insertion of <=200bp - G downstream_gene_variant PACA-AU 17 1324189 1324189 single base substitution C T 3_prime_UTR_variant PACA-AU 17 1324189 1324189 single base substitution C T downstream_gene_variant PACA-AU 17 1331101 1331101 single base substitution G A intron_variant PACA-AU 17 1331494 1331494 single base substitution C A intron_variant PACA-AU 17 1334790 1334790 single base substitution T G intron_variant PACA-AU 17 1339192 1339192 single base substitution G C intron_variant PACA-AU 17 1341987 1341987 single base substitution C T intron_variant PACA-AU 17 1342514 1342514 single base substitution C T intron_variant PACA-AU 17 1356237 1356237 deletion of <=200bp A - intron_variant PACA-AU 17 1359811 1359811 single base substitution G T intron_variant PACA-AU 17 1359811 1359811 single base substitution G T upstream_gene_variant PACA-AU 17 1366995 1366996 deletion of <=200bp AG - upstream_gene_variant PACA-CA 17 1319811 1319842 deletion of <=200bp AGCTGGGGATGGTGGTGTGCGCCTGTAGTCCC - downstream_gene_variant PACA-CA 17 1322486 1322486 single base substitution G C downstream_gene_variant PACA-CA 17 1325381 1325381 single base substitution A T 3_prime_UTR_variant PACA-CA 17 1325381 1325381 single base substitution A T downstream_gene_variant PACA-CA 17 1325521 1325521 single base substitution G A 3_prime_UTR_variant PACA-CA 17 1325521 1325521 single base substitution G A downstream_gene_variant PACA-CA 17 1327705 1327705 single base substitution C T intron_variant PACA-CA 17 1337651 1337651 single base substitution G T intron_variant PACA-CA 17 1339658 1339658 single base substitution G A intron_variant PACA-CA 17 1340992 1340992 single base substitution G C intron_variant PACA-CA 17 1347626 1347626 single base substitution A T intron_variant PACA-CA 17 1350547 1350547 single base substitution G A intron_variant PACA-CA 17 1354334 1354334 single base substitution A C intron_variant PACA-CA 17 1356618 1356618 insertion of <=200bp - A intron_variant PACA-CA 17 1357357 1357357 single base substitution G A intron_variant PACA-CA 17 1365907 1365907 single base substitution T G intron_variant PACA-CA 17 1366286 1366286 single base substitution A G exon_variant PACA-CA 17 1366438 1366438 single base substitution G A exon_variant PACA-CA 17 1368002 1368002 single base substitution C T upstream_gene_variant PACA-CA 17 1370639 1370639 single base substitution G T upstream_gene_variant PAEN-AU 17 1335790 1335790 single base substitution G A intron_variant PAEN-AU 17 1350727 1350727 single base substitution C T intron_variant PAEN-IT 17 1335604 1335604 single base substitution G A intron_variant PAEN-IT 17 1341652 1341652 single base substitution G A intron_variant PBCA-DE 17 1332148 1332148 deletion of <=200bp T - intron_variant PBCA-DE 17 1356533 1356533 single base substitution G C intron_variant PBCA-DE 17 1360177 1360177 single base substitution A T intron_variant PBCA-DE 17 1360177 1360177 single base substitution A T upstream_gene_variant PBCA-DE 17 1363849 1363849 single base substitution A T intron_variant PBCA-DE 17 1363849 1363849 single base substitution A T upstream_gene_variant PRAD-CA 17 1324121 1324121 single base substitution T C 3_prime_UTR_variant PRAD-CA 17 1324121 1324121 single base substitution T C downstream_gene_variant PRAD-CA 17 1331430 1331430 single base substitution T A intron_variant PRAD-UK 17 1332095 1332095 single base substitution C T intron_variant PRAD-UK 17 1342108 1342108 single base substitution C T intron_variant PRAD-UK 17 1347920 1347920 single base substitution C T intron_variant PRAD-UK 17 1353165 1353165 single base substitution A G intron_variant PRAD-UK 17 1357767 1357767 single base substitution G A intron_variant PRAD-UK 17 1361794 1361794 single base substitution G C intron_variant PRAD-UK 17 1361794 1361794 single base substitution G C upstream_gene_variant PRAD-UK 17 1367028 1367028 single base substitution G A upstream_gene_variant PRAD-US 17 1359240 1359240 single base substitution A C intron_variant PRAD-US 17 1359240 1359240 single base substitution A C missense_variant S58A 172T>G RECA-EU 17 1338520 1338520 single base substitution A G intron_variant RECA-EU 17 1340884 1340884 single base substitution C G intron_variant RECA-EU 17 1362777 1362777 single base substitution T C intron_variant RECA-EU 17 1362777 1362777 single base substitution T C upstream_gene_variant RECA-EU 17 1364242 1364242 single base substitution A C intron_variant RECA-EU 17 1364242 1364242 single base substitution A C upstream_gene_variant RECA-EU 17 1365092 1365092 single base substitution C T intron_variant SKCA-BR 17 1319621 1319621 insertion of <=200bp - GA downstream_gene_variant SKCA-BR 17 1320602 1320602 single base substitution C T downstream_gene_variant SKCA-BR 17 1321494 1321494 single base substitution G A downstream_gene_variant SKCA-BR 17 1327465 1327465 single base substitution A T intron_variant SKCA-BR 17 1328217 1328217 single base substitution T A intron_variant SKCA-BR 17 1328381 1328381 single base substitution G T intron_variant SKCA-BR 17 1331412 1331413 deletion of <=200bp CT - intron_variant SKCA-BR 17 1331802 1331802 single base substitution G A intron_variant SKCA-BR 17 1333354 1333354 single base substitution T A intron_variant SKCA-BR 17 1333826 1333826 insertion of <=200bp - AT intron_variant SKCA-BR 17 1335513 1335513 single base substitution T G intron_variant SKCA-BR 17 1335951 1335951 single base substitution G A intron_variant SKCA-BR 17 1337119 1337123 deletion of <=200bp GTTTT - intron_variant SKCA-BR 17 1337264 1337264 single base substitution G A intron_variant SKCA-BR 17 1338086 1338086 insertion of <=200bp - CAA intron_variant SKCA-BR 17 1339306 1339306 single base substitution C A intron_variant SKCA-BR 17 1342033 1342033 single base substitution C T intron_variant SKCA-BR 17 1343368 1343368 single base substitution T G intron_variant SKCA-BR 17 1343984 1343984 single base substitution A G intron_variant SKCA-BR 17 1347281 1347281 single base substitution A C intron_variant SKCA-BR 17 1347894 1347894 insertion of <=200bp - GGC intron_variant SKCA-BR 17 1349739 1349739 single base substitution A G intron_variant SKCA-BR 17 1350184 1350184 single base substitution G A intron_variant SKCA-BR 17 1351931 1351937 deletion of <=200bp AAAAAAG - intron_variant SKCA-BR 17 1351937 1351937 single base substitution G A intron_variant SKCA-BR 17 1353920 1353920 single base substitution T G intron_variant SKCA-BR 17 1357979 1357979 single base substitution C T intron_variant SKCA-BR 17 1359134 1359134 single base substitution A C intron_variant SKCA-BR 17 1359553 1359553 single base substitution T C intron_variant SKCA-BR 17 1359553 1359553 single base substitution T C upstream_gene_variant SKCA-BR 17 1361535 1361536 deletion of <=200bp CT - intron_variant SKCA-BR 17 1361535 1361536 deletion of <=200bp CT - upstream_gene_variant SKCA-BR 17 1362778 1362778 single base substitution T C intron_variant SKCA-BR 17 1362778 1362778 single base substitution T C upstream_gene_variant SKCA-BR 17 1369060 1369060 single base substitution G A upstream_gene_variant SKCA-BR 17 1370078 1370078 single base substitution G A upstream_gene_variant SKCA-BR 17 1371254 1371254 single base substitution C A upstream_gene_variant SKCM-US 17 1339973 1339973 single base substitution C A intron_variant SKCM-US 17 1339973 1339973 single base substitution C A missense_variant A240S 718G>T SKCM-US 17 1340006 1340006 single base substitution G A intron_variant SKCM-US 17 1340006 1340006 single base substitution G A missense_variant P229S 685C>T SKCM-US 17 1340138 1340138 single base substitution G A exon_variant SKCM-US 17 1340138 1340138 single base substitution G A intron_variant SKCM-US 17 1340138 1340138 single base substitution G A missense_variant P185S 553C>T SKCM-US 17 1340197 1340197 single base substitution G A exon_variant SKCM-US 17 1340197 1340197 single base substitution G A intron_variant SKCM-US 17 1340197 1340197 single base substitution G A missense_variant P165L 494C>T SKCM-US 17 1340235 1340235 single base substitution G C exon_variant SKCM-US 17 1340235 1340235 single base substitution G C intron_variant SKCM-US 17 1340235 1340235 single base substitution G C synonymous_variant P152P 456C>G SKCM-US 17 1340260 1340260 single base substitution T A exon_variant SKCM-US 17 1340260 1340260 single base substitution T A intron_variant SKCM-US 17 1340260 1340260 single base substitution T A missense_variant N144I 431A>T SKCM-US 17 1370616 1370616 single base substitution G A upstream_gene_variant SKCM-US 17 1371150 1371150 single base substitution G A upstream_gene_variant SKCM-US 17 1371284 1371284 single base substitution G A upstream_gene_variant STAD-US 17 1370578 1370578 single base substitution C T upstream_gene_variant STAD-US 17 1371157 1371157 single base substitution G A upstream_gene_variant THCA-SA 17 1359363 1359363 single base substitution T G intron_variant THCA-SA 17 1359363 1359363 single base substitution T G synonymous_variant R17R 49A>C UCEC-US 17 1340005 1340005 single base substitution G A intron_variant UCEC-US 17 1340005 1340005 single base substitution G A missense_variant P229L 686C>T UCEC-US 17 1340345 1340345 single base substitution C A exon_variant UCEC-US 17 1340345 1340345 single base substitution C A stop_gained E116* 346G>T UCEC-US 17 1370833 1370833 single base substitution C T upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand DLD1 COSM4623476 c.660C>A p.P220P Substitution - coding silent 17:1436737-1436737 - 470 COSM4437690 c.259C>G p.L87V Substitution - Missense 17:1437138-1437138 - PR-00-1165 COSM243848 c.646C>T p.P216S Substitution - Missense 17:1436751-1436751 - 08-P054 COSM4579448 c.401C>T p.A134V Substitution - Missense 17:1436996-1436996 - pfg143T COSM4748490 c.883G>C p.D295H Substitution - Missense 17:1423545-1423545 - 389 COSM4427608 c.15C>G p.F5L Substitution - Missense 17:1456103-1456103 - 86793 COSM95819 c.420C>G p.L140L Substitution - coding silent 17:1436977-1436977 - TCGA-AZ-6601-01 COSM1479244 c.485G>A p.R162Q Substitution - Missense 17:1436912-1436912 - NOKSI COSM4596129 c.466G>A p.G156R Substitution - Missense 17:1436931-1436931 - TCGA-G4-6321-01 COSM3755259 c.49A>C p.R17R Substitution - coding silent 17:1456069-1456069 - HCC29 COSM1609856 c.6G>A p.A2A Substitution - coding silent 17:1456112-1456112 - TCGA-12-0707 COSM2154449 c.854A>G p.H285R Substitution - Missense 17:1423574-1423574 - LUAD-S01302 COSM395625 c.84G>T p.Q28H Substitution - Missense 17:1456034-1456034 - TCGA-G4-6293-01 COSM3755259 c.49A>C p.R17R Substitution - coding silent 17:1456069-1456069 - TCGA-GF-A6C8-06 COSM3889335 c.718G>T p.A240S Substitution - Missense 17:1436679-1436679 - pfg019T COSM1640590 c.242-4_242-3insT p.? Unknown 17:1437158-1437159 - YUFIT COSM4263346 c.516G>A p.A172A Substitution - coding silent 17:1436881-1436881 - TCGA-DA-A1HV-06 COSM3514424 c.456C>G p.P152P Substitution - coding silent 17:1436941-1436941 - TCGA-AA-3715-01 COSM268948 c.558C>T p.Y186Y Substitution - coding silent 17:1436839-1436839 - TCGA-D1-A16R-01 COSM975638 c.686C>T p.P229L Substitution - Missense 17:1436711-1436711 - TCGA-D1-A17Q-01 COSM975640 c.346G>T p.E116* Substitution - Nonsense 17:1437051-1437051 - TCGA-EB-A3XD-01 COSM3514422 c.553C>T p.P185S Substitution - Missense 17:1436844-1436844 - PTC-70C COSM3755259 c.49A>C p.R17R Substitution - coding silent 17:1456069-1456069 - HX36T COSM1609856 c.6G>A p.A2A Substitution - coding silent 17:1456112-1456112 - TCGA-AR-A24X-01 COSM1479244 c.485G>A p.R162Q Substitution - Missense 17:1436912-1436912 - TCGA-AY-6386-01 COSM3755259 c.49A>C p.R17R Substitution - coding silent 17:1456069-1456069 - TCGA-B0-5107-01 COSM472319 c.807T>C p.I269I Substitution - coding silent 17:1423621-1423621 - ESCC_42 COSM5629694 c.228C>T p.A76A Substitution - coding silent 17:1455890-1455890 - CSCC-31-T COSM4490377 c.362C>T p.S121F Substitution - Missense 17:1437035-1437035 - T3118 COSM4674733 c.296C>T p.A99V Substitution - Missense 17:1437101-1437101 - CSCC-60-T COSM4558859 c.782G>T p.G261V Substitution - Missense 17:1423646-1423646 - 2521249 COSM5888321 c.629C>T p.P210L Substitution - Missense 17:1436768-1436768 - TCGA-EE-A29D-06 COSM3514425 c.431A>T p.N144I Substitution - Missense 17:1436966-1436966 - SNU-C4 COSM4652817 c.73G>A p.A25T Substitution - Missense 17:1456045-1456045 - PTC-7C COSM3755259 c.49A>C p.R17R Substitution - coding silent 17:1456069-1456069 - TCGA-AZ-4615-01 COSM3755259 c.49A>C p.R17R Substitution - coding silent 17:1456069-1456069 - TCGA-AA-3663-01 COSM3755259 c.49A>C p.R17R Substitution - coding silent 17:1456069-1456069 - TCGA-AY-6197-01 COSM3755259 c.49A>C p.R17R Substitution - coding silent 17:1456069-1456069 - TCGA-CH-5748-01 COSM1128823 c.172T>G p.S58A Substitution - Missense 17:1455946-1455946 - 112263 COSM94094 c.481A>T p.I161F Substitution - Missense 17:1436916-1436916 - TCGA-12-0707 COSM2154419 c.856T>A p.F286I Substitution - Missense 17:1423572-1423572 - CSCC-31-T COSM4505397 c.691C>T p.P231S Substitution - Missense 17:1436706-1436706 - 1287_T COSM3958030 c.373A>G p.S125G Substitution - Missense 17:1437024-1437024 - PTC-28C COSM3755259 c.49A>C p.R17R Substitution - coding silent 17:1456069-1456069 - TCGA-EE-A2MJ-06 COSM3514423 c.494C>T p.P165L Substitution - Missense 17:1436903-1436903 - HCC29T COSM1609856 c.6G>A p.A2A Substitution - coding silent 17:1456112-1456112 - T3080 COSM4674732 c.583G>A p.A195T Substitution - Missense 17:1436814-1436814 - 3N47-VS-3T47 COSM4982610 c.716A>T p.Y239F Substitution - Missense 17:1436681-1436681 - TCGA-12-0707 COSM2154432 c.850G>A p.G284S Substitution - Missense 17:1423578-1423578 - H650 COSM1194494 c.369G>C p.Q123H Substitution - Missense 17:1437028-1437028 - TCGA-AA-3662-01 COSM3755259 c.49A>C p.R17R Substitution - coding silent 17:1456069-1456069 - TCGA-C5-A7CL-01 COSM4837863 c.781G>A p.G261S Substitution - Missense 17:1423647-1423647 - PTC-515C COSM3755259 c.49A>C p.R17R Substitution - coding silent 17:1456069-1456069 - EGC15 COSM2738044 c.515C>T p.A172V Substitution - Missense 17:1436882-1436882 - LN229 COSM2738042 c.534G>T p.K178N Substitution - Missense 17:1436863-1436863 - TCGA-FR-A3R1-01 COSM3514419 c.685C>T p.P229S Substitution - Missense 17:1436712-1436712 - TCGA-12-0707 COSM2154447 c.855C>T p.H285H Substitution - coding silent 17:1423573-1423573 - TCGA-AA-3697-01 COSM3755259 c.49A>C p.R17R Substitution - coding silent 17:1456069-1456069 - TCGA-12-0707 COSM2154448 c.853C>A p.H285N Substitution - Missense 17:1423575-1423575 - TCGA-12-0707 COSM2154431 c.852T>C p.G284G Substitution - coding silent 17:1423576-1423576 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.461860;Hs.461867;Hs.461896 17p13.3 164762

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer - A 3-UTRInsertion . c.912+110dupT 17 1326700 RCCC - A 3-UTRInsertion . c.912+55dupT 17 1326756 STAD AAA - 3-UTRDeletion . c.912+53_912+55delTTT 17 1326755 STAD A C Missense p.S58A c.172T>G 17 1359240 PRAD A C Synonymous p.V118V c.354T>G 17 1340337 MM A G IntronicSNV . c.777+4134T>C 17 1335780 CLL A G Synonymous p.I269I c.807T>C 17 1326915 RCCC - A IntronicInsertion . c.242-5dupT 17 1340455 STAD C T Missense p.A2T c.4G>A 17 1359408 STAD C T Missense p.R162Q c.485G>A 17 1340206 BRCA C T Missense p.V187I c.559G>A 17 1340132 HNSC G A Missense p.P165L c.494C>T 17 1340197 CM G A Missense p.P229L c.686C>T 17 1340005 UCEC G A Missense p.S121F c.362C>T 17 1340329 CM G C Synonymous p.P152P c.456C>G 17 1340235 CM