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 BLCA 10 1118168 1118168 + Missense_Mutation SNP A A G TCGA-E7-A677-01A-11D-A30E-08 TCGA-E7-A677-10A-01D-A30H-08 g.chr10:1118168A>G c.73A>G c.(73-75)Ata>Gta p.I25V BLCA 10 1123867 1123867 + Silent SNP G G T TCGA-E7-A7PW-01A-11D-A34U-08 TCGA-E7-A7PW-10A-01D-A34X-08 g.chr10:1123867G>T c.159G>T c.(157-159)tcG>tcT p.S53S BLCA 10 1142135 1142135 + Silent SNP C C T TCGA-XF-A9ST-01A-11D-A42E-08 TCGA-XF-A9ST-10A-01D-A42H-08 g.chr10:1142135C>T c.675C>T c.(673-675)atC>atT p.I225I BLCA 10 1170267 1170267 + Missense_Mutation SNP A A T TCGA-2F-A9KQ-01A-11D-A38G-08 TCGA-2F-A9KQ-11A-11D-A38J-08 g.chr10:1170267A>T c.1213A>T c.(1213-1215)Att>Ttt p.I405F BRCA 10 1118202 1118202 + Missense_Mutation SNP C C T TCGA-AO-A03N-01B-11D-A10M-09 TCGA-AO-A03N-10A-01D-A10M-09 g.chr10:1118202C>T c.107C>T c.(106-108)aCg>aTg p.T36M BRCA 10 1123883 1123883 + Silent SNP C C T TCGA-BH-A0WA-01A-11D-A10G-09 TCGA-BH-A0WA-10A-01D-A117-09 g.chr10:1123883C>T c.175C>T c.(175-177)Ctg>Ttg p.L59L BRCA 10 1142162 1142162 + Silent SNP A A C TCGA-A2-A0T5-01A-21D-A099-09 TCGA-A2-A0T5-10A-01D-A099-09 g.chr10:1142162A>C c.702A>C c.(700-702)acA>acC p.T234T BRCA 10 1149703 1149703 + Silent SNP T T G TCGA-D8-A1XK-01A-21D-A14K-09 TCGA-D8-A1XK-10A-01D-A14K-09 g.chr10:1149703T>G c.888T>G c.(886-888)gcT>gcG p.A296A BRCA 10 1175216 1175216 + Missense_Mutation SNP A A C TCGA-A2-A0T5-01A-21D-A099-09 TCGA-A2-A0T5-10A-01D-A099-09 g.chr10:1175216A>C c.1417A>C c.(1417-1419)Acc>Ccc p.T473P CESC 10 1139409 1139409 + Missense_Mutation SNP C C T TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chr10:1139409C>T c.622C>T c.(622-624)Cat>Tat p.H208Y CESC 10 1142135 1142135 + Silent SNP C C T TCGA-EK-A2RA-01A-11D-A18J-09 TCGA-EK-A2RA-10A-01D-A18J-09 g.chr10:1142135C>T c.675C>T c.(673-675)atC>atT p.I225I CHOL 10 1170283 1170283 + Missense_Mutation SNP C C T TCGA-W5-AA2I-01A-32D-A417-09 TCGA-W5-AA2I-10A-01D-A41A-09 g.chr10:1170283C>T c.1229C>T c.(1228-1230)gCc>gTc p.A410V COAD 10 1149662 1149662 + Missense_Mutation SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr10:1149662G>A c.847G>A c.(847-849)Gtg>Atg p.V283M COAD 10 1170271 1170271 + Missense_Mutation SNP G G A TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr10:1170271G>A c.1217G>A c.(1216-1218)cGc>cAc p.R406H COAD 10 1170951 1170951 + Missense_Mutation SNP G G A TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr10:1170951G>A c.1340G>A c.(1339-1341)cGg>cAg p.R447Q COADREAD 10 1130478 1130478 + Splice_Site SNP G G A TCGA-AF-2687-01A-02D-1733-10 TCGA-AF-2687-10A-01D-1733-10 g.chr10:1130478G>A c.532G>A c.(532-534)Gat>Aat p.D178N COADREAD 10 1149662 1149662 + Missense_Mutation SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr10:1149662G>A c.847G>A c.(847-849)Gtg>Atg p.V283M COADREAD 10 1170271 1170271 + Missense_Mutation SNP G G A TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr10:1170271G>A c.1217G>A c.(1216-1218)cGc>cAc p.R406H COADREAD 10 1170951 1170951 + Missense_Mutation SNP G G A TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr10:1170951G>A c.1340G>A c.(1339-1341)cGg>cAg p.R447Q ESCA 10 1142172 1142172 + Missense_Mutation SNP G G T TCGA-LN-A4A3-01A-11D-A27G-09 TCGA-LN-A4A3-10A-01D-A27G-09 g.chr10:1142172G>T c.712G>T c.(712-714)Gtt>Ttt p.V238F ESCA 10 1170271 1170271 + Missense_Mutation SNP G G T TCGA-L5-A8NH-01A-11D-A37C-09 TCGA-L5-A8NH-11A-11D-A37F-09 g.chr10:1170271G>T c.1217G>T c.(1216-1218)cGc>cTc p.R406L GBMLGG 10 1149739 1149739 + Silent SNP C C T TCGA-TQ-A7RS-01A-12D-A33T-08 TCGA-TQ-A7RS-10A-01D-A33W-08 g.chr10:1149739C>T c.924C>T c.(922-924)taC>taT p.Y308Y HNSC 10 1123898 1123898 + Missense_Mutation SNP C C G TCGA-CV-7427-01A-11D-2078-08 TCGA-CV-7427-10A-01D-2078-08 g.chr10:1123898C>G c.190C>G c.(190-192)Caa>Gaa p.Q64E KICH 10 1175232 1175232 + Missense_Mutation SNP G G A TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr10:1175232G>A c.1433G>A c.(1432-1434)cGg>cAg p.R478Q KIPAN 10 1149775 1149775 + Splice_Site SNP A A C TCGA-B0-5107-01A-01D-1421-08 TCGA-B0-5107-11A-01D-1421-08 g.chr10:1149775A>C c.960A>C c.(958-960)acA>acC p.T320T KIPAN 10 1175232 1175232 + Missense_Mutation SNP G G A TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr10:1175232G>A c.1433G>A c.(1432-1434)cGg>cAg p.R478Q KIRC 10 1149775 1149775 + Splice_Site SNP A A C TCGA-B0-5107-01A-01D-1421-08 TCGA-B0-5107-11A-01D-1421-08 g.chr10:1149775A>C c.960A>C c.(958-960)acA>acC p.T320T LGG 10 1149739 1149739 + Silent SNP C C T TCGA-TQ-A7RS-01A-12D-A33T-08 TCGA-TQ-A7RS-10A-01D-A33W-08 g.chr10:1149739C>T c.924C>T c.(922-924)taC>taT p.Y308Y LIHC 10 1118109 1118109 + Missense_Mutation SNP G G C TCGA-WX-AA46-01A-11D-A38X-10 TCGA-WX-AA46-10A-01D-A38X-10 g.chr10:1118109G>C c.14G>C c.(13-15)aGc>aCc p.S5T LIHC 10 1149723 1149723 + Missense_Mutation SNP G G T TCGA-DD-A73G-01A-22D-A32G-10 TCGA-DD-A73G-10A-01D-A32G-10 g.chr10:1149723G>T c.908G>T c.(907-909)cGg>cTg p.R303L LIHC 10 1170240 1170240 + Frame_Shift_Del DEL A A - TCGA-G3-A3CJ-01A-11D-A20W-10 TCGA-G3-A3CJ-10A-01D-A20W-10 g.chr10:1170240delA c.1186delA c.(1186-1188)aaafs p.K396fs LUAD 10 1118122 1118122 + Silent SNP G G T TCGA-86-7955-01A-11D-2184-08 TCGA-86-7955-10A-01D-2184-08 g.chr10:1118122G>T c.27G>T c.(25-27)tcG>tcT p.S9S LUAD 10 1130413 1130413 + Missense_Mutation SNP G G T TCGA-78-7158-01A-11D-2036-08 TCGA-78-7158-10A-01D-2036-08 g.chr10:1130413G>T c.467G>T c.(466-468)cGg>cTg p.R156L LUAD 10 1170222 1170222 + Missense_Mutation SNP G G T TCGA-05-4382-01A-01D-1931-08 TCGA-05-4382-10A-01D-1265-08 g.chr10:1170222G>T c.1168G>T c.(1168-1170)Gtg>Ttg p.V390L LUAD 10 1170964 1170964 + Splice_Site SNP G G T TCGA-86-8073-01A-11D-2238-08 TCGA-86-8073-10A-01D-2238-08 g.chr10:1170964G>T c.1353G>T c.(1351-1353)caG>caT p.Q451H OV 10 1142163 1142163 + Missense_Mutation SNP C C A TCGA-30-1718-01A-01W-0633-09 TCGA-30-1718-10A-01W-0633-09 g.chr10:1142163C>A c.703C>A c.(703-705)Ccc>Acc p.P235T OV 10 1170258 1170258 + Missense_Mutation SNP A A G TCGA-23-2649-01A-01D-1526-09 TCGA-23-2649-10A-01D-1526-09 g.chr10:1170258A>G c.1204A>G c.(1204-1206)Att>Gtt p.I402V OV 10 1170849 1170849 + Splice_Site SNP G G A TCGA-29-1699-01A-01W-0633-09 TCGA-29-1699-10A-01W-0633-09 g.chr10:1170849G>A c.e13-1 PAAD 10 1132252 1132252 + Missense_Mutation SNP G G C TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr10:1132252G>C c.559G>C c.(559-561)Gag>Cag p.E187Q PAAD 10 1149626 1149626 + Missense_Mutation SNP C C A TCGA-2J-AAB1-01A-11D-A40W-08 TCGA-2J-AAB1-10A-01D-A40W-08 g.chr10:1149626C>A c.811C>A c.(811-813)Cgc>Agc p.R271S PAAD 10 1175231 1175231 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr10:1175231C>T c.1432C>T c.(1432-1434)Cgg>Tgg p.R478W PRAD 10 1142152 1142152 + Missense_Mutation SNP A A G TCGA-HC-7212-01A-11D-2114-08 TCGA-HC-7212-10A-01D-2115-08 g.chr10:1142152A>G c.692A>G c.(691-693)cAg>cGg p.Q231R PRAD 10 1149689 1149689 + Frame_Shift_Del DEL G G - TCGA-EJ-7782-01A-11D-2114-08 TCGA-EJ-7782-10A-01D-2114-08 g.chr10:1149689delG c.874delG c.(874-876)gggfs p.G293fs READ 10 1130478 1130478 + Splice_Site SNP G G A TCGA-AF-2687-01A-02D-1733-10 TCGA-AF-2687-10A-01D-1733-10 g.chr10:1130478G>A c.532G>A c.(532-534)Gat>Aat p.D178N SKCM 10 1126377 1126377 + Silent SNP C C A TCGA-GF-A6C8-06A-12D-A30X-08 TCGA-GF-A6C8-10A-01D-A30X-08 g.chr10:1126377C>A c.357C>A c.(355-357)tcC>tcA p.S119S SKCM 10 1149546 1149546 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr10:1149546C>T c.731C>T c.(730-732)tCt>tTt p.S244F SKCM 10 1175199 1175199 + Missense_Mutation SNP C C T TCGA-EB-A5UL-06A-11D-A30X-08 TCGA-EB-A5UL-10A-01D-A30X-08 g.chr10:1175199C>T c.1400C>T c.(1399-1401)cCc>cTc p.P467L SKCM 10 1175199 1175199 + Missense_Mutation SNP C C T TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr10:1175199C>T c.1400C>T c.(1399-1401)cCc>cTc p.P467L

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BRCA-EU 10 1090782 1090782 single base substitution C T upstream_gene_variant BRCA-EU 10 1092456 1092456 single base substitution C T upstream_gene_variant BRCA-EU 10 1094291 1094291 single base substitution C A upstream_gene_variant BRCA-EU 10 1094406 1094406 single base substitution C T upstream_gene_variant BRCA-EU 10 1094940 1094940 single base substitution A T upstream_gene_variant BRCA-EU 10 1095043 1095043 single base substitution G C upstream_gene_variant BRCA-EU 10 1096239 1096240 deletion of <=200bp TC - intron_variant BRCA-EU 10 1097399 1097399 single base substitution C A intron_variant BRCA-EU 10 1097399 1097399 single base substitution C A upstream_gene_variant BRCA-EU 10 1097519 1097519 single base substitution C T intron_variant BRCA-EU 10 1097519 1097519 single base substitution C T upstream_gene_variant BRCA-EU 10 1097642 1097642 single base substitution C A intron_variant BRCA-EU 10 1097642 1097642 single base substitution C A upstream_gene_variant BRCA-EU 10 1098206 1098206 single base substitution C G intron_variant BRCA-EU 10 1098206 1098206 single base substitution C G upstream_gene_variant BRCA-EU 10 1098399 1098399 single base substitution C A intron_variant BRCA-EU 10 1098399 1098399 single base substitution C A upstream_gene_variant BRCA-EU 10 1101122 1101122 single base substitution T G intron_variant BRCA-EU 10 1101122 1101122 single base substitution T G upstream_gene_variant BRCA-EU 10 1101532 1101532 single base substitution C G intron_variant BRCA-EU 10 1101532 1101532 single base substitution C G upstream_gene_variant BRCA-EU 10 1102624 1102624 single base substitution C T intron_variant BRCA-EU 10 1102624 1102624 single base substitution C T upstream_gene_variant BRCA-EU 10 1103338 1103343 deletion of <=200bp TGCGTC - intron_variant BRCA-EU 10 1104740 1104740 single base substitution C G intron_variant BRCA-EU 10 1109384 1109384 single base substitution C A intron_variant BRCA-EU 10 1110453 1110453 single base substitution T A intron_variant BRCA-EU 10 1111828 1111828 single base substitution C T intron_variant BRCA-EU 10 1112508 1112508 single base substitution C T intron_variant BRCA-EU 10 1114545 1114545 single base substitution A G intron_variant BRCA-EU 10 1115390 1115390 single base substitution G A intron_variant BRCA-EU 10 1115390 1115390 single base substitution G A upstream_gene_variant BRCA-EU 10 1115421 1115421 single base substitution A T intron_variant BRCA-EU 10 1115421 1115421 single base substitution A T upstream_gene_variant BRCA-EU 10 1115771 1115771 single base substitution T C intron_variant BRCA-EU 10 1115771 1115771 single base substitution T C upstream_gene_variant BRCA-EU 10 1115810 1115810 single base substitution G T intron_variant BRCA-EU 10 1115810 1115810 single base substitution G T upstream_gene_variant BRCA-EU 10 1117074 1117074 single base substitution C T intron_variant BRCA-EU 10 1117074 1117074 single base substitution C T upstream_gene_variant BRCA-EU 10 1117867 1117867 single base substitution A C intron_variant BRCA-EU 10 1117867 1117867 single base substitution A C upstream_gene_variant BRCA-EU 10 1117981 1117981 single base substitution C G intron_variant BRCA-EU 10 1117981 1117981 single base substitution C G upstream_gene_variant BRCA-EU 10 1118487 1118487 single base substitution C G intron_variant BRCA-EU 10 1118487 1118487 single base substitution C G upstream_gene_variant BRCA-EU 10 1120017 1120017 single base substitution C G intron_variant BRCA-EU 10 1120017 1120017 single base substitution C G upstream_gene_variant BRCA-EU 10 1120645 1120645 single base substitution G A intron_variant BRCA-EU 10 1120802 1120802 single base substitution C T intron_variant BRCA-EU 10 1121836 1121836 single base substitution C G intron_variant BRCA-EU 10 1126849 1126849 single base substitution A G intron_variant BRCA-EU 10 1127060 1127060 single base substitution A T intron_variant BRCA-EU 10 1127323 1127323 single base substitution C T intron_variant BRCA-EU 10 1128314 1128314 single base substitution C A intron_variant BRCA-EU 10 1129468 1129468 single base substitution C G intron_variant BRCA-EU 10 1129773 1129773 single base substitution G A intron_variant BRCA-EU 10 1130353 1130353 single base substitution G T missense_variant S103I 308G>T BRCA-EU 10 1130353 1130353 single base substitution G T missense_variant S136I 407G>T BRCA-EU 10 1132518 1132518 single base substitution C T intron_variant BRCA-EU 10 1132999 1132999 single base substitution C G intron_variant BRCA-EU 10 1133521 1133521 single base substitution C T intron_variant BRCA-EU 10 1135357 1135357 single base substitution C T intron_variant BRCA-EU 10 1136345 1136345 single base substitution C T intron_variant BRCA-EU 10 1137068 1137068 single base substitution C G intron_variant BRCA-EU 10 1139441 1139441 single base substitution G A splice_region_variant BRCA-EU 10 1139764 1139764 single base substitution C G intron_variant BRCA-EU 10 1140542 1140542 single base substitution G A intron_variant BRCA-EU 10 1141013 1141013 single base substitution T C intron_variant BRCA-EU 10 1141014 1141014 single base substitution G A intron_variant BRCA-EU 10 1141031 1141031 single base substitution G A intron_variant BRCA-EU 10 1141305 1141305 single base substitution A G intron_variant BRCA-EU 10 1142104 1142104 single base substitution C G intron_variant BRCA-EU 10 1142104 1142104 single base substitution C G splice_region_variant BRCA-EU 10 1142156 1142156 single base substitution G A synonymous_variant L199L 597G>A BRCA-EU 10 1142156 1142156 single base substitution G A synonymous_variant L232L 696G>A BRCA-EU 10 1144997 1144997 single base substitution T C downstream_gene_variant BRCA-EU 10 1144997 1144997 single base substitution T C intron_variant BRCA-EU 10 1146090 1146090 single base substitution C T downstream_gene_variant BRCA-EU 10 1146090 1146090 single base substitution C T intron_variant BRCA-EU 10 1146354 1146354 single base substitution T C downstream_gene_variant BRCA-EU 10 1146354 1146354 single base substitution T C intron_variant BRCA-EU 10 1147465 1147465 single base substitution A T downstream_gene_variant BRCA-EU 10 1147465 1147465 single base substitution A T intron_variant BRCA-EU 10 1148404 1148404 single base substitution C G intron_variant BRCA-EU 10 1150157 1150157 single base substitution C G intron_variant BRCA-EU 10 1150414 1150414 single base substitution G T intron_variant BRCA-EU 10 1151020 1151020 single base substitution C T intron_variant BRCA-EU 10 1151654 1151654 single base substitution G A intron_variant BRCA-EU 10 1151696 1151696 single base substitution C G intron_variant BRCA-EU 10 1151734 1151734 deletion of <=200bp T - intron_variant BRCA-EU 10 1152425 1152425 single base substitution A C intron_variant BRCA-EU 10 1153116 1153116 single base substitution C T intron_variant BRCA-EU 10 1154454 1154454 single base substitution C T intron_variant BRCA-EU 10 1154815 1154815 single base substitution A C intron_variant BRCA-EU 10 1155226 1155226 single base substitution A G intron_variant BRCA-EU 10 1156472 1156472 single base substitution G C intron_variant BRCA-EU 10 1156695 1156695 single base substitution G A intron_variant BRCA-EU 10 1157334 1157334 single base substitution C G intron_variant BRCA-EU 10 1157760 1157760 single base substitution G T intron_variant BRCA-EU 10 1158814 1158814 single base substitution C A intron_variant BRCA-EU 10 1159288 1159289 deletion of <=200bp CT - intron_variant BRCA-EU 10 1160417 1160417 deletion of <=200bp T - intron_variant BRCA-EU 10 1161869 1161869 single base substitution C T intron_variant BRCA-EU 10 1163902 1163902 single base substitution C G intron_variant BRCA-EU 10 1163979 1163979 single base substitution C T intron_variant BRCA-EU 10 1165005 1165005 single base substitution G C intron_variant BRCA-EU 10 1165005 1165005 single base substitution G C upstream_gene_variant BRCA-EU 10 1165178 1165178 single base substitution G A intron_variant BRCA-EU 10 1165178 1165178 single base substitution G A upstream_gene_variant BRCA-EU 10 1165336 1165336 single base substitution C G intron_variant BRCA-EU 10 1165336 1165336 single base substitution C G upstream_gene_variant BRCA-EU 10 1165640 1165640 single base substitution G T intron_variant BRCA-EU 10 1165640 1165640 single base substitution G T upstream_gene_variant BRCA-EU 10 1165717 1165717 single base substitution G A intron_variant BRCA-EU 10 1165717 1165717 single base substitution G A upstream_gene_variant BRCA-EU 10 1165875 1165875 single base substitution G A intron_variant BRCA-EU 10 1165875 1165875 single base substitution G A upstream_gene_variant BRCA-EU 10 1166960 1166960 single base substitution C T intron_variant BRCA-EU 10 1166960 1166960 single base substitution C T upstream_gene_variant BRCA-EU 10 1167354 1167354 single base substitution C T intron_variant BRCA-EU 10 1167354 1167354 single base substitution C T upstream_gene_variant BRCA-EU 10 1168901 1168901 deletion of <=200bp T - intron_variant BRCA-EU 10 1168901 1168901 deletion of <=200bp T - upstream_gene_variant BRCA-EU 10 1169483 1169483 deletion of <=200bp T - intron_variant BRCA-EU 10 1169483 1169483 deletion of <=200bp T - upstream_gene_variant BRCA-EU 10 1169573 1169573 single base substitution G A intron_variant BRCA-EU 10 1169573 1169573 single base substitution G A upstream_gene_variant BRCA-EU 10 1170809 1170809 single base substitution C T intron_variant BRCA-EU 10 1172820 1172820 single base substitution T G intron_variant BRCA-EU 10 1173348 1173348 single base substitution T C intron_variant BRCA-EU 10 1174216 1174216 single base substitution A C intron_variant BRCA-EU 10 1174734 1174734 single base substitution G A intron_variant BRCA-EU 10 1175635 1175635 single base substitution G A 3_prime_UTR_variant BRCA-EU 10 1175635 1175635 single base substitution G A downstream_gene_variant BRCA-EU 10 1175701 1175701 single base substitution C A 3_prime_UTR_variant BRCA-EU 10 1175701 1175701 single base substitution C A downstream_gene_variant BRCA-EU 10 1176759 1176759 single base substitution C A 3_prime_UTR_variant BRCA-EU 10 1176759 1176759 single base substitution C A downstream_gene_variant BRCA-EU 10 1180925 1180926 deletion of <=200bp AA - downstream_gene_variant BRCA-EU 10 1181318 1181318 single base substitution C G downstream_gene_variant BRCA-EU 10 1181799 1181799 single base substitution C G downstream_gene_variant BRCA-EU 10 1181977 1181977 single base substitution G T downstream_gene_variant BRCA-EU 10 1182928 1182928 single base substitution G A downstream_gene_variant BRCA-FR 10 1117074 1117074 single base substitution C T intron_variant BRCA-FR 10 1117074 1117074 single base substitution C T upstream_gene_variant BRCA-FR 10 1117981 1117981 single base substitution C G intron_variant BRCA-FR 10 1117981 1117981 single base substitution C G upstream_gene_variant BRCA-FR 10 1121836 1121836 single base substitution C G intron_variant BRCA-FR 10 1125437 1125437 single base substitution G C intron_variant BRCA-FR 10 1130353 1130353 single base substitution G T missense_variant S103I 308G>T BRCA-FR 10 1130353 1130353 single base substitution G T missense_variant S136I 407G>T BRCA-FR 10 1135357 1135357 single base substitution C T intron_variant BRCA-FR 10 1136345 1136345 single base substitution C T intron_variant BRCA-FR 10 1151696 1151696 single base substitution C G intron_variant BRCA-FR 10 1161869 1161869 single base substitution C T intron_variant BRCA-FR 10 1165640 1165640 single base substitution G T intron_variant BRCA-FR 10 1165640 1165640 single base substitution G T upstream_gene_variant BRCA-FR 10 1175635 1175635 single base substitution G A 3_prime_UTR_variant BRCA-FR 10 1175635 1175635 single base substitution G A downstream_gene_variant BRCA-KR 10 1094075 1094075 single base substitution A T upstream_gene_variant BRCA-UK 10 1091011 1091011 single base substitution C T upstream_gene_variant BRCA-UK 10 1103297 1103297 single base substitution C T intron_variant BRCA-UK 10 1120802 1120802 single base substitution C T intron_variant BRCA-UK 10 1132999 1132999 single base substitution C G intron_variant BRCA-UK 10 1141305 1141305 single base substitution A G intron_variant BRCA-UK 10 1156695 1156695 single base substitution G A intron_variant BRCA-UK 10 1157760 1157760 single base substitution G T intron_variant BRCA-UK 10 1159648 1159648 single base substitution C T intron_variant BRCA-US 10 1094228 1094228 single base substitution C T upstream_gene_variant BRCA-US 10 1094816 1094816 single base substitution C T upstream_gene_variant BRCA-US 10 1118202 1118202 single base substitution C T missense_variant T36M 107C>T BRCA-US 10 1118202 1118202 single base substitution C T upstream_gene_variant BRCA-US 10 1123883 1123883 single base substitution C T synonymous_variant L26L 76C>T BRCA-US 10 1123883 1123883 single base substitution C T synonymous_variant L59L 175C>T BRCA-US 10 1142162 1142162 single base substitution A C synonymous_variant T201T 603A>C BRCA-US 10 1142162 1142162 single base substitution A C synonymous_variant T234T 702A>C BRCA-US 10 1149703 1149703 single base substitution T G synonymous_variant A296A 888T>G BRCA-US 10 1175216 1175216 single base substitution A C downstream_gene_variant BRCA-US 10 1175216 1175216 single base substitution A C missense_variant T473P 1417A>C BTCA-JP 10 1094899 1094899 single base substitution G A upstream_gene_variant BTCA-JP 10 1120335 1120335 single base substitution G A 5_prime_UTR_variant BTCA-JP 10 1120335 1120335 single base substitution G A intron_variant BTCA-JP 10 1151146 1151146 single base substitution C T missense_variant R348C 1042C>T CESC-US 10 1139409 1139409 single base substitution C T missense_variant H175Y 523C>T CESC-US 10 1139409 1139409 single base substitution C T missense_variant H208Y 622C>T CESC-US 10 1142135 1142135 single base substitution C T synonymous_variant I192I 576C>T CESC-US 10 1142135 1142135 single base substitution C T synonymous_variant I225I 675C>T CLLE-ES 10 1105867 1105867 single base substitution C G intron_variant CLLE-ES 10 1113712 1113712 single base substitution A G intron_variant CLLE-ES 10 1127107 1127108 deletion of <=200bp AG - intron_variant CLLE-ES 10 1153179 1153179 single base substitution T C intron_variant CLLE-ES 10 1171385 1171385 single base substitution G A intron_variant COAD-US 10 1094906 1094906 single base substitution C T upstream_gene_variant COAD-US 10 1094909 1094909 single base substitution C G upstream_gene_variant COAD-US 10 1149662 1149662 single base substitution G A missense_variant V283M 847G>A COAD-US 10 1170271 1170271 single base substitution G A exon_variant COAD-US 10 1170271 1170271 single base substitution G A missense_variant R406H 1217G>A COAD-US 10 1170951 1170951 single base substitution G A exon_variant COAD-US 10 1170951 1170951 single base substitution G A missense_variant R447Q 1340G>A COCA-CN 10 1094164 1094164 single base substitution A C upstream_gene_variant COCA-CN 10 1100746 1100746 single base substitution G T intron_variant COCA-CN 10 1100746 1100746 single base substitution G T upstream_gene_variant COCA-CN 10 1107885 1107885 single base substitution T C intron_variant COCA-CN 10 1118372 1118372 single base substitution A G intron_variant COCA-CN 10 1118372 1118372 single base substitution A G upstream_gene_variant COCA-CN 10 1135578 1135578 single base substitution A T intron_variant COCA-CN 10 1135630 1135630 single base substitution G A intron_variant COCA-CN 10 1135661 1135661 single base substitution A G intron_variant COCA-CN 10 1136900 1136900 single base substitution G A intron_variant COCA-CN 10 1145670 1145670 single base substitution T C downstream_gene_variant COCA-CN 10 1145670 1145670 single base substitution T C intron_variant COCA-CN 10 1148018 1148018 single base substitution T C intron_variant COCA-CN 10 1148208 1148208 single base substitution C T intron_variant COCA-CN 10 1148219 1148219 single base substitution C T intron_variant COCA-CN 10 1148252 1148252 single base substitution T C intron_variant COCA-CN 10 1149677 1149677 single base substitution G A missense_variant D288N 862G>A COCA-CN 10 1153562 1153562 single base substitution C T intron_variant COCA-CN 10 1162174 1162174 single base substitution C T intron_variant COCA-CN 10 1164314 1164314 single base substitution A G intron_variant COCA-CN 10 1164487 1164487 single base substitution T C intron_variant COCA-CN 10 1169015 1169015 single base substitution C T intron_variant COCA-CN 10 1169015 1169015 single base substitution C T upstream_gene_variant COCA-CN 10 1175086 1175086 single base substitution C T intron_variant EOPC-DE 10 1135565 1135565 single base substitution A G intron_variant EOPC-DE 10 1148006 1148006 single base substitution A C intron_variant EOPC-DE 10 1148168 1148168 single base substitution C T intron_variant EOPC-DE 10 1163826 1163826 single base substitution G A intron_variant EOPC-DE 10 1163827 1163827 single base substitution T C intron_variant EOPC-DE 10 1164487 1164487 single base substitution T C intron_variant EOPC-DE 10 1176187 1176187 single base substitution C T 3_prime_UTR_variant EOPC-DE 10 1176187 1176187 single base substitution C T downstream_gene_variant ESAD-UK 10 1090988 1090988 single base substitution C T upstream_gene_variant ESAD-UK 10 1096364 1096364 single base substitution C G intron_variant ESAD-UK 10 1099937 1099937 single base substitution A C intron_variant ESAD-UK 10 1099937 1099937 single base substitution A C upstream_gene_variant ESAD-UK 10 1101171 1101171 single base substitution C T intron_variant ESAD-UK 10 1101171 1101171 single base substitution C T upstream_gene_variant ESAD-UK 10 1103905 1103905 single base substitution C T intron_variant ESAD-UK 10 1106134 1106134 single base substitution A G intron_variant ESAD-UK 10 1113525 1113525 single base substitution T C intron_variant ESAD-UK 10 1113651 1113651 single base substitution C T intron_variant ESAD-UK 10 1113857 1113857 single base substitution C T intron_variant ESAD-UK 10 1118477 1118477 single base substitution C G intron_variant ESAD-UK 10 1118477 1118477 single base substitution C G upstream_gene_variant ESAD-UK 10 1118716 1118716 insertion of <=200bp - ACA intron_variant ESAD-UK 10 1118716 1118716 insertion of <=200bp - ACA upstream_gene_variant ESAD-UK 10 1124339 1124339 deletion of <=200bp T - intron_variant ESAD-UK 10 1126496 1126496 single base substitution A G intron_variant ESAD-UK 10 1126510 1126510 single base substitution G A intron_variant ESAD-UK 10 1127919 1127919 single base substitution A G intron_variant ESAD-UK 10 1129121 1129121 single base substitution G A intron_variant ESAD-UK 10 1131608 1131608 single base substitution C T intron_variant ESAD-UK 10 1132254 1132254 single base substitution G A synonymous_variant E154E 462G>A ESAD-UK 10 1132254 1132254 single base substitution G A synonymous_variant E187E 561G>A ESAD-UK 10 1136360 1136360 single base substitution A G intron_variant ESAD-UK 10 1136980 1136980 single base substitution A G intron_variant ESAD-UK 10 1137657 1137657 single base substitution G T intron_variant ESAD-UK 10 1138479 1138479 single base substitution T G intron_variant ESAD-UK 10 1138733 1138733 single base substitution C T intron_variant ESAD-UK 10 1139613 1139613 single base substitution T A intron_variant ESAD-UK 10 1139908 1139908 single base substitution A C intron_variant ESAD-UK 10 1142158 1142158 single base substitution C T missense_variant P200L 599C>T ESAD-UK 10 1142158 1142158 single base substitution C T missense_variant P233L 698C>T ESAD-UK 10 1143148 1143148 deletion of <=200bp A - downstream_gene_variant ESAD-UK 10 1143148 1143148 deletion of <=200bp A - intron_variant ESAD-UK 10 1144993 1144993 single base substitution C T downstream_gene_variant ESAD-UK 10 1144993 1144993 single base substitution C T intron_variant ESAD-UK 10 1145141 1145141 single base substitution T C downstream_gene_variant ESAD-UK 10 1145141 1145141 single base substitution T C intron_variant ESAD-UK 10 1145496 1145496 single base substitution T G downstream_gene_variant ESAD-UK 10 1145496 1145496 single base substitution T G intron_variant ESAD-UK 10 1148168 1148168 single base substitution C T intron_variant ESAD-UK 10 1148252 1148252 single base substitution T C intron_variant ESAD-UK 10 1150244 1150244 single base substitution G C intron_variant ESAD-UK 10 1150809 1150809 single base substitution G T intron_variant ESAD-UK 10 1151034 1151034 single base substitution G T intron_variant ESAD-UK 10 1152084 1152084 single base substitution G A intron_variant ESAD-UK 10 1152596 1152596 single base substitution A C intron_variant ESAD-UK 10 1153097 1153097 single base substitution G A intron_variant ESAD-UK 10 1154340 1154340 single base substitution T G intron_variant ESAD-UK 10 1157847 1157847 insertion of <=200bp - C intron_variant ESAD-UK 10 1158518 1158518 single base substitution C G intron_variant ESAD-UK 10 1159244 1159244 insertion of <=200bp - T intron_variant ESAD-UK 10 1159326 1159326 single base substitution A C intron_variant ESAD-UK 10 1163212 1163212 single base substitution C T intron_variant ESAD-UK 10 1163648 1163648 single base substitution G A intron_variant ESAD-UK 10 1176485 1176485 single base substitution G C 3_prime_UTR_variant ESAD-UK 10 1176485 1176485 single base substitution G C downstream_gene_variant ESAD-UK 10 1177634 1177634 insertion of <=200bp - GC 3_prime_UTR_variant ESAD-UK 10 1177634 1177634 insertion of <=200bp - GC downstream_gene_variant ESAD-UK 10 1179286 1179286 insertion of <=200bp - A downstream_gene_variant ESAD-UK 10 1181953 1181953 single base substitution T C downstream_gene_variant ESAD-UK 10 1182777 1182777 insertion of <=200bp - T downstream_gene_variant ESAD-UK 10 1183125 1183125 single base substitution C T downstream_gene_variant ESCA-CN 10 1170179 1170179 single base substitution C A exon_variant ESCA-CN 10 1170179 1170179 single base substitution C A missense_variant F375L 1125C>A KIRC-US 10 1149775 1149775 single base substitution A C splice_region_variant LAML-KR 10 1137870 1137870 single base substitution T C intron_variant LAML-KR 10 1141353 1141353 single base substitution C T intron_variant LAML-KR 10 1160957 1160957 single base substitution A G intron_variant LAML-KR 10 1164313 1164313 single base substitution C T intron_variant LGG-US 10 1170957 1170957 single base substitution G T exon_variant LGG-US 10 1170957 1170957 single base substitution G T missense_variant S449I 1346G>T LICA-FR 10 1096108 1096147 deletion of <=200bp TACTAACATAGAAATTAAACATATTAAAATATTCACTTAA - intron_variant LICA-FR 10 1101920 1101920 single base substitution T C intron_variant LICA-FR 10 1101920 1101920 single base substitution T C upstream_gene_variant LICA-FR 10 1101997 1101997 single base substitution T G intron_variant LICA-FR 10 1101997 1101997 single base substitution T G upstream_gene_variant LICA-FR 10 1113488 1113488 insertion of <=200bp - TAAA intron_variant LICA-FR 10 1116762 1116762 single base substitution A T intron_variant LICA-FR 10 1116762 1116762 single base substitution A T upstream_gene_variant LICA-FR 10 1117771 1117771 single base substitution A T intron_variant LICA-FR 10 1117771 1117771 single base substitution A T upstream_gene_variant LICA-FR 10 1122941 1122941 deletion of <=200bp A - intron_variant LICA-FR 10 1123550 1123550 single base substitution A T intron_variant LICA-FR 10 1128386 1128386 insertion of <=200bp - T intron_variant LICA-FR 10 1138568 1138568 single base substitution T G intron_variant LICA-FR 10 1142152 1142152 single base substitution A T missense_variant Q198L 593A>T LICA-FR 10 1142152 1142152 single base substitution A T missense_variant Q231L 692A>T LIHC-US 10 1149723 1149723 single base substitution G T missense_variant R303L 908G>T LINC-JP 10 1092039 1092039 single base substitution T A upstream_gene_variant LINC-JP 10 1093959 1093959 insertion of <=200bp - T upstream_gene_variant LINC-JP 10 1094900 1094900 single base substitution G A upstream_gene_variant LINC-JP 10 1094902 1094902 single base substitution C A upstream_gene_variant LINC-JP 10 1096323 1096323 single base substitution T A intron_variant LINC-JP 10 1101340 1101340 single base substitution A C intron_variant LINC-JP 10 1101340 1101340 single base substitution A C upstream_gene_variant LINC-JP 10 1124069 1124069 single base substitution C G intron_variant LINC-JP 10 1137249 1137249 single base substitution A G intron_variant LINC-JP 10 1142119 1142119 single base substitution A T missense_variant D187V 560A>T LINC-JP 10 1142119 1142119 single base substitution A T missense_variant D220V 659A>T LINC-JP 10 1142898 1142898 single base substitution G A downstream_gene_variant LINC-JP 10 1142898 1142898 single base substitution G A intron_variant LINC-JP 10 1148168 1148168 single base substitution C T intron_variant LINC-JP 10 1149559 1149559 single base substitution A G synonymous_variant E248E 744A>G LINC-JP 10 1163779 1163779 single base substitution T G intron_variant LINC-JP 10 1182964 1182964 single base substitution C T downstream_gene_variant LIRI-JP 10 1090896 1090896 single base substitution T C upstream_gene_variant LIRI-JP 10 1093942 1093942 deletion of <=200bp A - upstream_gene_variant LIRI-JP 10 1094142 1094142 single base substitution A G upstream_gene_variant LIRI-JP 10 1096135 1096135 single base substitution A C intron_variant LIRI-JP 10 1097049 1097049 single base substitution C T intron_variant LIRI-JP 10 1098033 1098033 single base substitution G T intron_variant LIRI-JP 10 1098033 1098033 single base substitution G T upstream_gene_variant LIRI-JP 10 1098185 1098185 single base substitution C T intron_variant LIRI-JP 10 1098185 1098185 single base substitution C T upstream_gene_variant LIRI-JP 10 1100712 1100712 single base substitution T G intron_variant LIRI-JP 10 1100712 1100712 single base substitution T G upstream_gene_variant LIRI-JP 10 1100774 1100774 single base substitution T G intron_variant LIRI-JP 10 1100774 1100774 single base substitution T G upstream_gene_variant LIRI-JP 10 1104970 1104970 single base substitution A G intron_variant LIRI-JP 10 1105383 1105383 single base substitution A G intron_variant LIRI-JP 10 1105418 1105418 single base substitution C A intron_variant LIRI-JP 10 1107041 1107041 single base substitution C A intron_variant LIRI-JP 10 1110420 1110420 single base substitution T A intron_variant LIRI-JP 10 1114474 1114474 single base substitution C T intron_variant LIRI-JP 10 1115653 1115653 single base substitution A G intron_variant LIRI-JP 10 1115653 1115653 single base substitution A G upstream_gene_variant LIRI-JP 10 1120795 1120795 single base substitution G A intron_variant LIRI-JP 10 1122251 1122251 single base substitution T C intron_variant LIRI-JP 10 1124966 1124966 single base substitution G A intron_variant LIRI-JP 10 1126453 1126453 single base substitution G T intron_variant LIRI-JP 10 1130340 1130340 single base substitution C T splice_region_variant LIRI-JP 10 1131512 1131512 single base substitution C T intron_variant LIRI-JP 10 1131979 1131979 single base substitution A C intron_variant LIRI-JP 10 1132083 1132083 single base substitution A G intron_variant LIRI-JP 10 1134163 1134163 single base substitution A T intron_variant LIRI-JP 10 1135005 1135005 single base substitution G T intron_variant LIRI-JP 10 1136447 1136447 single base substitution G A intron_variant LIRI-JP 10 1139163 1139163 single base substitution T C intron_variant LIRI-JP 10 1139173 1139173 single base substitution G A intron_variant LIRI-JP 10 1140323 1140323 single base substitution G A intron_variant LIRI-JP 10 1142295 1142295 single base substitution A G 3_prime_UTR_variant LIRI-JP 10 1142295 1142295 single base substitution A G downstream_gene_variant LIRI-JP 10 1142295 1142295 single base substitution A G intron_variant LIRI-JP 10 1142782 1142782 single base substitution A G downstream_gene_variant LIRI-JP 10 1142782 1142782 single base substitution A G intron_variant LIRI-JP 10 1143671 1143671 single base substitution C T downstream_gene_variant LIRI-JP 10 1143671 1143671 single base substitution C T intron_variant LIRI-JP 10 1144596 1144596 single base substitution G T downstream_gene_variant LIRI-JP 10 1144596 1144596 single base substitution G T intron_variant LIRI-JP 10 1145563 1145563 single base substitution G T downstream_gene_variant LIRI-JP 10 1145563 1145563 single base substitution G T intron_variant LIRI-JP 10 1146227 1146227 insertion of <=200bp - CACTGCA downstream_gene_variant LIRI-JP 10 1146227 1146227 insertion of <=200bp - CACTGCA intron_variant LIRI-JP 10 1149967 1149967 single base substitution G A intron_variant LIRI-JP 10 1151176 1151176 single base substitution C A missense_variant H358N 1072C>A LIRI-JP 10 1154273 1154273 single base substitution T G intron_variant LIRI-JP 10 1155184 1155184 single base substitution G A intron_variant LIRI-JP 10 1155517 1155517 single base substitution G A intron_variant LIRI-JP 10 1155824 1155828 deletion of <=200bp TCCTA - intron_variant LIRI-JP 10 1156089 1156089 single base substitution G A intron_variant LIRI-JP 10 1156517 1156517 single base substitution G A intron_variant LIRI-JP 10 1157668 1157668 single base substitution A G intron_variant LIRI-JP 10 1159470 1159470 single base substitution T C intron_variant LIRI-JP 10 1162631 1162631 single base substitution T C intron_variant LIRI-JP 10 1164767 1164767 single base substitution G A intron_variant LIRI-JP 10 1164767 1164767 single base substitution G A upstream_gene_variant LIRI-JP 10 1168292 1168292 single base substitution T A intron_variant LIRI-JP 10 1168292 1168292 single base substitution T A upstream_gene_variant LIRI-JP 10 1168976 1168976 single base substitution T C intron_variant LIRI-JP 10 1168976 1168976 single base substitution T C upstream_gene_variant LIRI-JP 10 1169862 1169862 single base substitution A C exon_variant LIRI-JP 10 1169862 1169862 single base substitution A C intron_variant LIRI-JP 10 1169978 1169978 single base substitution T C exon_variant LIRI-JP 10 1169978 1169978 single base substitution T C intron_variant LIRI-JP 10 1170703 1170703 single base substitution A G intron_variant LIRI-JP 10 1172686 1172686 single base substitution G T intron_variant LIRI-JP 10 1175296 1175296 single base substitution G A 3_prime_UTR_variant LIRI-JP 10 1175296 1175296 single base substitution G A downstream_gene_variant LIRI-JP 10 1175784 1175784 single base substitution A G 3_prime_UTR_variant LIRI-JP 10 1175784 1175784 single base substitution A G downstream_gene_variant LIRI-JP 10 1178341 1178341 insertion of <=200bp - A downstream_gene_variant LIRI-JP 10 1178411 1178411 single base substitution A G downstream_gene_variant LIRI-JP 10 1179044 1179044 single base substitution A G downstream_gene_variant LIRI-JP 10 1179070 1179070 single base substitution C A downstream_gene_variant LIRI-JP 10 1179690 1179690 single base substitution A C downstream_gene_variant LIRI-JP 10 1181111 1181111 single base substitution A G downstream_gene_variant LIRI-JP 10 1182267 1182267 single base substitution A G downstream_gene_variant LUSC-KR 10 1095117 1095117 single base substitution C A upstream_gene_variant LUSC-KR 10 1096886 1096886 single base substitution C G intron_variant LUSC-KR 10 1107208 1107208 single base substitution A G intron_variant LUSC-KR 10 1116654 1116654 single base substitution C G intron_variant LUSC-KR 10 1116654 1116654 single base substitution C G upstream_gene_variant LUSC-KR 10 1118740 1118740 single base substitution G T intron_variant LUSC-KR 10 1118740 1118740 single base substitution G T upstream_gene_variant LUSC-KR 10 1118809 1118809 single base substitution A T intron_variant LUSC-KR 10 1118809 1118809 single base substitution A T upstream_gene_variant LUSC-KR 10 1120709 1120709 single base substitution A T intron_variant LUSC-KR 10 1122511 1122511 single base substitution C T intron_variant LUSC-KR 10 1132691 1132691 single base substitution G T intron_variant LUSC-KR 10 1135929 1135929 single base substitution C A intron_variant LUSC-KR 10 1136651 1136651 single base substitution G T intron_variant LUSC-KR 10 1140118 1140118 single base substitution C T intron_variant LUSC-KR 10 1146689 1146689 single base substitution C T downstream_gene_variant LUSC-KR 10 1146689 1146689 single base substitution C T intron_variant LUSC-KR 10 1151749 1151749 single base substitution G T intron_variant LUSC-KR 10 1152802 1152802 single base substitution C T intron_variant LUSC-KR 10 1160089 1160089 single base substitution G T intron_variant LUSC-KR 10 1161444 1161444 single base substitution C T intron_variant LUSC-KR 10 1163971 1163971 single base substitution T C intron_variant LUSC-KR 10 1164461 1164461 single base substitution G T intron_variant LUSC-KR 10 1167282 1167282 single base substitution G T intron_variant LUSC-KR 10 1167282 1167282 single base substitution G T upstream_gene_variant LUSC-KR 10 1167691 1167691 single base substitution C G intron_variant LUSC-KR 10 1167691 1167691 single base substitution C G upstream_gene_variant LUSC-KR 10 1175894 1175894 single base substitution A G 3_prime_UTR_variant LUSC-KR 10 1175894 1175894 single base substitution A G downstream_gene_variant LUSC-KR 10 1177633 1177633 single base substitution T C 3_prime_UTR_variant LUSC-KR 10 1177633 1177633 single base substitution T C downstream_gene_variant LUSC-KR 10 1179291 1179291 single base substitution A T downstream_gene_variant MALY-DE 10 1094252 1094252 single base substitution G A upstream_gene_variant MALY-DE 10 1098550 1098550 single base substitution C T intron_variant MALY-DE 10 1098550 1098550 single base substitution C T upstream_gene_variant MALY-DE 10 1100757 1100757 single base substitution T G intron_variant MALY-DE 10 1100757 1100757 single base substitution T G upstream_gene_variant MALY-DE 10 1107627 1107627 single base substitution A C intron_variant MALY-DE 10 1111834 1111834 deletion of <=200bp T - intron_variant MALY-DE 10 1114975 1114975 single base substitution G A intron_variant MALY-DE 10 1121488 1121488 single base substitution A C intron_variant MALY-DE 10 1132113 1132113 single base substitution G A intron_variant MALY-DE 10 1135591 1135591 single base substitution G A intron_variant MALY-DE 10 1135630 1135630 single base substitution G A intron_variant MALY-DE 10 1139631 1139631 single base substitution A T intron_variant MALY-DE 10 1139632 1139632 single base substitution G T intron_variant MALY-DE 10 1144662 1144662 single base substitution T C downstream_gene_variant MALY-DE 10 1144662 1144662 single base substitution T C intron_variant MALY-DE 10 1151258 1151258 single base substitution G A intron_variant MALY-DE 10 1165696 1165696 single base substitution G A intron_variant MALY-DE 10 1165696 1165696 single base substitution G A upstream_gene_variant MALY-DE 10 1170768 1170768 single base substitution C T intron_variant MALY-DE 10 1174611 1174611 single base substitution G A intron_variant MALY-DE 10 1182616 1182616 single base substitution C T downstream_gene_variant MELA-AU 10 1090680 1090680 single base substitution T C upstream_gene_variant MELA-AU 10 1090787 1090787 single base substitution G A upstream_gene_variant MELA-AU 10 1091002 1091002 insertion of <=200bp - A upstream_gene_variant MELA-AU 10 1094642 1094642 single base substitution C T upstream_gene_variant MELA-AU 10 1094863 1094863 single base substitution G C upstream_gene_variant MELA-AU 10 1095117 1095117 single base substitution C T upstream_gene_variant MELA-AU 10 1096806 1096806 single base substitution C T intron_variant MELA-AU 10 1099865 1099865 single base substitution G A intron_variant MELA-AU 10 1099865 1099865 single base substitution G A upstream_gene_variant MELA-AU 10 1100130 1100130 single base substitution G A intron_variant MELA-AU 10 1100130 1100130 single base substitution G A upstream_gene_variant MELA-AU 10 1101586 1101586 single base substitution T C intron_variant MELA-AU 10 1101586 1101586 single base substitution T C upstream_gene_variant MELA-AU 10 1102133 1102133 single base substitution G A intron_variant MELA-AU 10 1102133 1102133 single base substitution G A upstream_gene_variant MELA-AU 10 1102224 1102224 single base substitution A G intron_variant MELA-AU 10 1102224 1102224 single base substitution A G upstream_gene_variant MELA-AU 10 1102746 1102746 single base substitution G A intron_variant MELA-AU 10 1102746 1102746 single base substitution G A upstream_gene_variant MELA-AU 10 1103346 1103346 single base substitution C T intron_variant MELA-AU 10 1104184 1104184 single base substitution C T intron_variant MELA-AU 10 1105570 1105570 single base substitution C T intron_variant MELA-AU 10 1105948 1105948 single base substitution T A intron_variant MELA-AU 10 1106656 1106656 single base substitution C T intron_variant MELA-AU 10 1108596 1108596 single base substitution C T intron_variant MELA-AU 10 1112362 1112362 single base substitution T G intron_variant MELA-AU 10 1114221 1114221 single base substitution A G intron_variant MELA-AU 10 1114296 1114296 insertion of <=200bp - CTGTAGTCCCAGCCACTCGGGAGG intron_variant MELA-AU 10 1117872 1117872 single base substitution C T intron_variant MELA-AU 10 1117872 1117872 single base substitution C T upstream_gene_variant MELA-AU 10 1118674 1118675 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 1118674 1118675 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 10 1118681 1118681 single base substitution C T intron_variant MELA-AU 10 1118681 1118681 single base substitution C T upstream_gene_variant MELA-AU 10 1119894 1119894 single base substitution A G intron_variant MELA-AU 10 1119894 1119894 single base substitution A G upstream_gene_variant MELA-AU 10 1120794 1120794 single base substitution C T intron_variant MELA-AU 10 1121415 1121415 single base substitution C T intron_variant MELA-AU 10 1121417 1121417 single base substitution C T intron_variant MELA-AU 10 1121888 1121888 single base substitution T A intron_variant MELA-AU 10 1122259 1122259 single base substitution C T intron_variant MELA-AU 10 1122822 1122822 single base substitution C T intron_variant MELA-AU 10 1123922 1123922 single base substitution C T missense_variant L39F 115C>T MELA-AU 10 1123922 1123922 single base substitution C T missense_variant L72F 214C>T MELA-AU 10 1123930 1123930 single base substitution C T synonymous_variant I41I 123C>T MELA-AU 10 1123930 1123930 single base substitution C T synonymous_variant I74I 222C>T MELA-AU 10 1125325 1125325 single base substitution C T intron_variant MELA-AU 10 1125401 1125401 single base substitution C T intron_variant MELA-AU 10 1125598 1125598 single base substitution C T intron_variant MELA-AU 10 1128892 1128892 single base substitution T A intron_variant MELA-AU 10 1129138 1129138 single base substitution T C intron_variant MELA-AU 10 1129602 1129602 single base substitution C T intron_variant MELA-AU 10 1130390 1130390 single base substitution C T synonymous_variant L115L 345C>T MELA-AU 10 1130390 1130390 single base substitution C T synonymous_variant L148L 444C>T MELA-AU 10 1130531 1130531 single base substitution C T intron_variant MELA-AU 10 1132332 1132332 single base substitution C T intron_variant MELA-AU 10 1133118 1133119 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 1133192 1133192 single base substitution C T intron_variant MELA-AU 10 1133205 1133205 single base substitution C T intron_variant MELA-AU 10 1133425 1133425 single base substitution C T intron_variant MELA-AU 10 1133479 1133479 single base substitution T C intron_variant MELA-AU 10 1133760 1133760 single base substitution C G intron_variant MELA-AU 10 1134046 1134046 single base substitution C T intron_variant MELA-AU 10 1136560 1136560 single base substitution C T intron_variant MELA-AU 10 1136654 1136654 single base substitution T G intron_variant MELA-AU 10 1137347 1137347 single base substitution C T intron_variant MELA-AU 10 1138508 1138508 single base substitution C T intron_variant MELA-AU 10 1138850 1138850 single base substitution C T intron_variant MELA-AU 10 1139612 1139612 single base substitution C T intron_variant MELA-AU 10 1139945 1139945 single base substitution C T intron_variant MELA-AU 10 1140817 1140817 single base substitution G A intron_variant MELA-AU 10 1142314 1142315 multiple base substitution (>=2bp and <=200bp) CC TT 3_prime_UTR_variant MELA-AU 10 1142314 1142315 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 10 1142314 1142315 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 1142440 1142440 single base substitution C T 3_prime_UTR_variant MELA-AU 10 1142440 1142440 single base substitution C T downstream_gene_variant MELA-AU 10 1142440 1142440 single base substitution C T intron_variant MELA-AU 10 1142490 1142490 single base substitution C T 3_prime_UTR_variant MELA-AU 10 1142490 1142490 single base substitution C T downstream_gene_variant MELA-AU 10 1142490 1142490 single base substitution C T intron_variant MELA-AU 10 1142558 1142558 single base substitution T G 3_prime_UTR_variant MELA-AU 10 1142558 1142558 single base substitution T G downstream_gene_variant MELA-AU 10 1142558 1142558 single base substitution T G intron_variant MELA-AU 10 1143000 1143000 single base substitution C T downstream_gene_variant MELA-AU 10 1143000 1143000 single base substitution C T intron_variant MELA-AU 10 1143212 1143212 single base substitution G C downstream_gene_variant MELA-AU 10 1143212 1143212 single base substitution G C intron_variant MELA-AU 10 1144569 1144569 single base substitution T C downstream_gene_variant MELA-AU 10 1144569 1144569 single base substitution T C intron_variant MELA-AU 10 1146063 1146063 single base substitution A C downstream_gene_variant MELA-AU 10 1146063 1146063 single base substitution A C intron_variant MELA-AU 10 1146125 1146125 single base substitution C T downstream_gene_variant MELA-AU 10 1146125 1146125 single base substitution C T intron_variant MELA-AU 10 1146464 1146464 single base substitution C T downstream_gene_variant MELA-AU 10 1146464 1146464 single base substitution C T intron_variant MELA-AU 10 1146765 1146765 single base substitution C T downstream_gene_variant MELA-AU 10 1146765 1146765 single base substitution C T intron_variant MELA-AU 10 1146814 1146814 single base substitution C T downstream_gene_variant MELA-AU 10 1146814 1146814 single base substitution C T intron_variant MELA-AU 10 1146856 1146856 single base substitution C T downstream_gene_variant MELA-AU 10 1146856 1146856 single base substitution C T intron_variant MELA-AU 10 1148270 1148270 single base substitution C T intron_variant MELA-AU 10 1149693 1149694 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant G293E 878GG>AA MELA-AU 10 1149945 1149945 single base substitution A G intron_variant MELA-AU 10 1150365 1150365 single base substitution T C intron_variant MELA-AU 10 1150959 1150959 single base substitution T C intron_variant MELA-AU 10 1151171 1151171 single base substitution C T missense_variant S356F 1067C>T MELA-AU 10 1151283 1151283 single base substitution G A intron_variant MELA-AU 10 1151463 1151463 single base substitution T G intron_variant MELA-AU 10 1151502 1151502 single base substitution C T intron_variant MELA-AU 10 1151952 1151952 single base substitution C T intron_variant MELA-AU 10 1152019 1152019 single base substitution C T intron_variant MELA-AU 10 1152075 1152075 single base substitution C T intron_variant MELA-AU 10 1152189 1152189 single base substitution C T intron_variant MELA-AU 10 1152491 1152491 single base substitution C T intron_variant MELA-AU 10 1152594 1152595 deletion of <=200bp TT - intron_variant MELA-AU 10 1153125 1153125 single base substitution C T intron_variant MELA-AU 10 1153453 1153453 single base substitution C T intron_variant MELA-AU 10 1154484 1154484 single base substitution C T intron_variant MELA-AU 10 1154766 1154766 single base substitution C T intron_variant MELA-AU 10 1155902 1155902 single base substitution C T intron_variant MELA-AU 10 1156144 1156144 single base substitution C T intron_variant MELA-AU 10 1156242 1156242 single base substitution C T intron_variant MELA-AU 10 1156406 1156406 single base substitution A T intron_variant MELA-AU 10 1156582 1156582 single base substitution G A intron_variant MELA-AU 10 1158285 1158285 single base substitution C T intron_variant MELA-AU 10 1158320 1158320 single base substitution C T intron_variant MELA-AU 10 1159162 1159162 single base substitution G A intron_variant MELA-AU 10 1161497 1161497 single base substitution C T intron_variant MELA-AU 10 1161527 1161527 single base substitution T A intron_variant MELA-AU 10 1161880 1161880 single base substitution C T intron_variant MELA-AU 10 1162448 1162448 single base substitution C T intron_variant MELA-AU 10 1162882 1162882 single base substitution C T intron_variant MELA-AU 10 1163479 1163479 single base substitution C T intron_variant MELA-AU 10 1163927 1163927 single base substitution C T intron_variant MELA-AU 10 1164528 1164528 single base substitution C T intron_variant MELA-AU 10 1164637 1164637 single base substitution C T intron_variant MELA-AU 10 1165163 1165163 single base substitution A G intron_variant MELA-AU 10 1165163 1165163 single base substitution A G upstream_gene_variant MELA-AU 10 1165810 1165810 single base substitution C T intron_variant MELA-AU 10 1165810 1165810 single base substitution C T upstream_gene_variant MELA-AU 10 1165889 1165889 single base substitution C T intron_variant MELA-AU 10 1165889 1165889 single base substitution C T upstream_gene_variant MELA-AU 10 1167173 1167174 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 10 1167173 1167174 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 10 1167910 1167911 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 1167910 1167911 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 10 1169061 1169061 single base substitution C A intron_variant MELA-AU 10 1169061 1169061 single base substitution C A upstream_gene_variant MELA-AU 10 1169462 1169462 single base substitution C T intron_variant MELA-AU 10 1169462 1169462 single base substitution C T upstream_gene_variant MELA-AU 10 1171151 1171151 single base substitution C T intron_variant MELA-AU 10 1171198 1171198 single base substitution C T intron_variant MELA-AU 10 1171929 1171929 single base substitution C T intron_variant MELA-AU 10 1172774 1172774 single base substitution C T intron_variant MELA-AU 10 1172865 1172865 single base substitution G T intron_variant MELA-AU 10 1173975 1173975 single base substitution C T intron_variant MELA-AU 10 1174672 1174673 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 10 1174999 1174999 single base substitution C T intron_variant MELA-AU 10 1175035 1175035 single base substitution C T intron_variant MELA-AU 10 1175046 1175046 single base substitution C T intron_variant MELA-AU 10 1175654 1175654 single base substitution C T 3_prime_UTR_variant MELA-AU 10 1175654 1175654 single base substitution C T downstream_gene_variant MELA-AU 10 1176133 1176133 single base substitution C T 3_prime_UTR_variant MELA-AU 10 1176133 1176133 single base substitution C T downstream_gene_variant MELA-AU 10 1176678 1176678 single base substitution G A 3_prime_UTR_variant MELA-AU 10 1176678 1176678 single base substitution G A downstream_gene_variant MELA-AU 10 1177574 1177574 single base substitution C T 3_prime_UTR_variant MELA-AU 10 1177574 1177574 single base substitution C T downstream_gene_variant MELA-AU 10 1177635 1177635 single base substitution T C 3_prime_UTR_variant MELA-AU 10 1177635 1177635 single base substitution T C downstream_gene_variant MELA-AU 10 1178482 1178482 single base substitution C T downstream_gene_variant MELA-AU 10 1178997 1178997 single base substitution C T downstream_gene_variant MELA-AU 10 1179613 1179613 single base substitution G A downstream_gene_variant MELA-AU 10 1179654 1179654 single base substitution G A downstream_gene_variant MELA-AU 10 1179776 1179776 single base substitution G C downstream_gene_variant MELA-AU 10 1179890 1179890 single base substitution G A downstream_gene_variant MELA-AU 10 1180422 1180422 single base substitution G A downstream_gene_variant MELA-AU 10 1180800 1180800 single base substitution A G downstream_gene_variant MELA-AU 10 1181208 1181208 single base substitution A G downstream_gene_variant MELA-AU 10 1181503 1181503 single base substitution C T downstream_gene_variant MELA-AU 10 1181504 1181504 single base substitution C T downstream_gene_variant MELA-AU 10 1181778 1181778 single base substitution G A downstream_gene_variant MELA-AU 10 1181990 1181990 single base substitution T C downstream_gene_variant MELA-AU 10 1182314 1182314 single base substitution C T downstream_gene_variant MELA-AU 10 1182765 1182765 single base substitution A G downstream_gene_variant MELA-AU 10 1182961 1182961 single base substitution C T downstream_gene_variant MELA-AU 10 1182990 1182990 single base substitution C T downstream_gene_variant ORCA-IN 10 1118815 1118815 single base substitution G T intron_variant ORCA-IN 10 1118815 1118815 single base substitution G T upstream_gene_variant ORCA-IN 10 1130422 1130422 single base substitution T C missense_variant I126T 377T>C ORCA-IN 10 1130422 1130422 single base substitution T C missense_variant I159T 476T>C ORCA-IN 10 1135608 1135608 single base substitution G A intron_variant ORCA-IN 10 1135630 1135630 single base substitution G A intron_variant ORCA-IN 10 1142584 1142584 single base substitution G A downstream_gene_variant ORCA-IN 10 1142584 1142584 single base substitution G A intron_variant ORCA-IN 10 1160866 1160866 single base substitution C T intron_variant ORCA-IN 10 1170960 1170960 single base substitution G T exon_variant ORCA-IN 10 1170960 1170960 single base substitution G T missense_variant R450L 1349G>T OV-AU 10 1091455 1091455 single base substitution G A upstream_gene_variant OV-AU 10 1091840 1091840 single base substitution C T upstream_gene_variant OV-AU 10 1102926 1102926 single base substitution C T intron_variant OV-AU 10 1107342 1107342 single base substitution G A intron_variant OV-AU 10 1120923 1120923 single base substitution C A intron_variant OV-AU 10 1124157 1124157 single base substitution A G intron_variant OV-AU 10 1125126 1125126 single base substitution G A intron_variant OV-AU 10 1129019 1129019 single base substitution T A intron_variant OV-AU 10 1130509 1130509 single base substitution G A intron_variant OV-AU 10 1135234 1135234 single base substitution C G intron_variant OV-AU 10 1136031 1136031 single base substitution C T intron_variant OV-AU 10 1142270 1142270 single base substitution G A 3_prime_UTR_variant OV-AU 10 1142270 1142270 single base substitution G A downstream_gene_variant OV-AU 10 1142270 1142270 single base substitution G A intron_variant OV-AU 10 1144288 1144288 single base substitution G C downstream_gene_variant OV-AU 10 1144288 1144288 single base substitution G C intron_variant OV-AU 10 1149245 1149245 single base substitution T C intron_variant OV-AU 10 1151097 1151097 single base substitution A T synonymous_variant T331T 993A>T OV-AU 10 1151764 1151764 single base substitution C T intron_variant OV-AU 10 1154149 1154149 single base substitution G T intron_variant OV-AU 10 1154155 1154155 single base substitution G A intron_variant OV-AU 10 1155173 1155173 single base substitution C G intron_variant OV-AU 10 1159966 1159966 single base substitution G A intron_variant OV-AU 10 1164650 1164650 single base substitution A T intron_variant OV-AU 10 1167586 1167586 single base substitution T G intron_variant OV-AU 10 1167586 1167586 single base substitution T G upstream_gene_variant OV-AU 10 1174885 1174885 single base substitution C T intron_variant OV-AU 10 1175931 1175931 single base substitution C G 3_prime_UTR_variant OV-AU 10 1175931 1175931 single base substitution C G downstream_gene_variant OV-AU 10 1176437 1176437 single base substitution C G 3_prime_UTR_variant OV-AU 10 1176437 1176437 single base substitution C G downstream_gene_variant OV-AU 10 1182257 1182257 single base substitution T C downstream_gene_variant PACA-AU 10 1094833 1094833 single base substitution C G upstream_gene_variant PACA-AU 10 1095404 1095405 deletion of <=200bp CC - upstream_gene_variant PACA-AU 10 1101989 1101989 deletion of <=200bp C - intron_variant PACA-AU 10 1101989 1101989 deletion of <=200bp C - upstream_gene_variant PACA-AU 10 1103395 1103395 single base substitution C T intron_variant PACA-AU 10 1108162 1108162 single base substitution A T intron_variant PACA-AU 10 1108255 1108255 single base substitution G A intron_variant PACA-AU 10 1109498 1109498 single base substitution C T intron_variant PACA-AU 10 1114296 1114296 insertion of <=200bp - CTGTAGTCCCAGCCACTCGGGAGG intron_variant PACA-AU 10 1118171 1118171 single base substitution C T stop_gained R26* 76C>T PACA-AU 10 1118171 1118171 single base substitution C T upstream_gene_variant PACA-AU 10 1126333 1126333 single base substitution T C intron_variant PACA-AU 10 1126716 1126716 single base substitution G A intron_variant PACA-AU 10 1132045 1132045 single base substitution C T intron_variant PACA-AU 10 1135538 1135538 single base substitution C T intron_variant PACA-AU 10 1137294 1137294 single base substitution T C intron_variant PACA-AU 10 1144245 1144245 single base substitution C G downstream_gene_variant PACA-AU 10 1144245 1144245 single base substitution C G intron_variant PACA-AU 10 1145902 1145902 single base substitution T C downstream_gene_variant PACA-AU 10 1145902 1145902 single base substitution T C intron_variant PACA-AU 10 1151146 1151146 single base substitution C T missense_variant R348C 1042C>T PACA-AU 10 1154863 1154863 single base substitution G A intron_variant PACA-AU 10 1156810 1156810 single base substitution A G intron_variant PACA-AU 10 1161679 1161679 single base substitution C T intron_variant PACA-AU 10 1164374 1164374 single base substitution G A intron_variant PACA-AU 10 1168456 1168456 single base substitution C T intron_variant PACA-AU 10 1168456 1168456 single base substitution C T upstream_gene_variant PACA-AU 10 1174817 1174817 single base substitution C T intron_variant PACA-AU 10 1176344 1176344 single base substitution G A 3_prime_UTR_variant PACA-AU 10 1176344 1176344 single base substitution G A downstream_gene_variant PACA-AU 10 1178555 1178555 single base substitution G A downstream_gene_variant PACA-AU 10 1182298 1182298 single base substitution C A downstream_gene_variant PACA-CA 10 1093989 1093989 single base substitution G C upstream_gene_variant PACA-CA 10 1096101 1096101 single base substitution T C intron_variant PACA-CA 10 1096513 1096513 single base substitution T C intron_variant PACA-CA 10 1097179 1097179 single base substitution C T intron_variant PACA-CA 10 1099080 1099080 single base substitution T A intron_variant PACA-CA 10 1099080 1099080 single base substitution T A upstream_gene_variant PACA-CA 10 1101004 1101032 deletion of <=200bp CAATAAATTTGTTTAAGCTGCCTAGTTTG - intron_variant PACA-CA 10 1101004 1101032 deletion of <=200bp CAATAAATTTGTTTAAGCTGCCTAGTTTG - upstream_gene_variant PACA-CA 10 1102119 1102119 single base substitution G T intron_variant PACA-CA 10 1102119 1102119 single base substitution G T upstream_gene_variant PACA-CA 10 1104425 1104425 single base substitution T G intron_variant PACA-CA 10 1112424 1112424 single base substitution C G intron_variant PACA-CA 10 1113797 1113797 single base substitution G A intron_variant PACA-CA 10 1118831 1118831 single base substitution T C intron_variant PACA-CA 10 1118831 1118831 single base substitution T C upstream_gene_variant PACA-CA 10 1120447 1120447 single base substitution C T intron_variant PACA-CA 10 1120447 1120447 single base substitution C T missense_variant S13F 38C>T PACA-CA 10 1122008 1122008 single base substitution C T intron_variant PACA-CA 10 1124416 1124416 single base substitution C T intron_variant PACA-CA 10 1134898 1134898 single base substitution T A intron_variant PACA-CA 10 1136074 1136074 insertion of <=200bp - T intron_variant PACA-CA 10 1136753 1136753 single base substitution G A intron_variant PACA-CA 10 1136764 1136764 single base substitution G A intron_variant PACA-CA 10 1139011 1139011 single base substitution T C intron_variant PACA-CA 10 1140323 1140324 deletion of <=200bp GG - intron_variant PACA-CA 10 1140325 1140325 insertion of <=200bp - ACAG intron_variant PACA-CA 10 1140329 1140342 deletion of <=200bp GTTTAAGAAGGAGC - intron_variant PACA-CA 10 1140331 1140331 insertion of <=200bp - CCCAG intron_variant PACA-CA 10 1140335 1140335 deletion of <=200bp G - intron_variant PACA-CA 10 1140341 1140343 deletion of <=200bp GCC - intron_variant PACA-CA 10 1140387 1140387 single base substitution C T intron_variant PACA-CA 10 1145202 1145202 single base substitution G A downstream_gene_variant PACA-CA 10 1145202 1145202 single base substitution G A intron_variant PACA-CA 10 1147699 1147699 single base substitution T C intron_variant PACA-CA 10 1151432 1151432 single base substitution C G intron_variant PACA-CA 10 1151795 1151795 single base substitution G T intron_variant PACA-CA 10 1151940 1151940 single base substitution T G intron_variant PACA-CA 10 1159259 1159259 single base substitution G A intron_variant PACA-CA 10 1163690 1163690 single base substitution G A intron_variant PACA-CA 10 1167391 1167391 single base substitution C G intron_variant PACA-CA 10 1167391 1167391 single base substitution C G upstream_gene_variant PACA-CA 10 1175096 1175098 deletion of <=200bp TTA - intron_variant PACA-CA 10 1175102 1175102 insertion of <=200bp - G intron_variant PACA-CA 10 1175107 1175111 deletion of <=200bp CTTTC - intron_variant PACA-CA 10 1179762 1179762 single base substitution C T downstream_gene_variant PACA-CA 10 1180662 1180662 single base substitution A T downstream_gene_variant PACA-CA 10 1180719 1180719 single base substitution G C downstream_gene_variant PAEN-AU 10 1114296 1114296 insertion of <=200bp - CTGTAGTCCCAGCCACTCGGGAGG intron_variant PAEN-AU 10 1147881 1147881 single base substitution T A intron_variant PAEN-AU 10 1163855 1163855 single base substitution C T intron_variant PAEN-IT 10 1127479 1127479 single base substitution G T intron_variant PAEN-IT 10 1141623 1141623 single base substitution G A intron_variant PAEN-IT 10 1143819 1143819 single base substitution G A downstream_gene_variant PAEN-IT 10 1143819 1143819 single base substitution G A intron_variant PAEN-IT 10 1152560 1152560 single base substitution G T intron_variant PAEN-IT 10 1162925 1162925 single base substitution A G intron_variant PBCA-DE 10 1098452 1098452 single base substitution T C intron_variant PBCA-DE 10 1098452 1098452 single base substitution T C upstream_gene_variant PBCA-DE 10 1101798 1101798 single base substitution G C intron_variant PBCA-DE 10 1101798 1101798 single base substitution G C upstream_gene_variant PBCA-DE 10 1111178 1111178 single base substitution G A intron_variant PBCA-DE 10 1125482 1125482 deletion of <=200bp T - intron_variant PBCA-DE 10 1126684 1126684 insertion of <=200bp - AA intron_variant PBCA-DE 10 1130139 1130139 single base substitution G A intron_variant PBCA-DE 10 1137301 1137301 single base substitution C G intron_variant PBCA-DE 10 1148168 1148168 single base substitution C T intron_variant PBCA-DE 10 1148177 1148177 single base substitution A T intron_variant PBCA-DE 10 1152041 1152041 single base substitution G T intron_variant PBCA-DE 10 1165889 1165889 single base substitution C A intron_variant PBCA-DE 10 1165889 1165889 single base substitution C A upstream_gene_variant PBCA-DE 10 1166786 1166787 deletion of <=200bp TC - intron_variant PBCA-DE 10 1166786 1166787 deletion of <=200bp TC - upstream_gene_variant PBCA-DE 10 1170974 1170974 single base substitution C T intron_variant PRAD-CA 10 1117518 1117518 single base substitution C T intron_variant PRAD-CA 10 1117518 1117518 single base substitution C T upstream_gene_variant PRAD-CA 10 1133046 1133046 single base substitution T C intron_variant PRAD-CA 10 1135646 1135646 single base substitution C T intron_variant PRAD-CA 10 1142913 1142913 single base substitution C T downstream_gene_variant PRAD-CA 10 1142913 1142913 single base substitution C T intron_variant PRAD-CA 10 1148252 1148252 single base substitution T C intron_variant PRAD-CA 10 1158192 1158192 single base substitution A G intron_variant PRAD-CA 10 1167525 1167525 single base substitution G A intron_variant PRAD-CA 10 1167525 1167525 single base substitution G A upstream_gene_variant PRAD-CA 10 1173539 1173539 single base substitution C T intron_variant PRAD-UK 10 1113224 1113224 single base substitution A G intron_variant PRAD-UK 10 1134164 1134164 single base substitution T G intron_variant PRAD-UK 10 1140899 1140963 multiple base substitution (>=2bp and <=200bp) AAGGGAGAGTTAGACTGAGAAACGTGAGGTGATGGGGATAGCGAGGAGGGTTAGACTGGGAAACA AGGAGGGAGTTAGACTGGGAATG intron_variant PRAD-UK 10 1154307 1154307 single base substitution C G intron_variant PRAD-UK 10 1156771 1156771 single base substitution C T intron_variant PRAD-UK 10 1164453 1164453 single base substitution C T intron_variant PRAD-UK 10 1164854 1164854 single base substitution T C intron_variant PRAD-UK 10 1164854 1164854 single base substitution T C upstream_gene_variant PRAD-UK 10 1169210 1169210 single base substitution A G intron_variant PRAD-UK 10 1169210 1169210 single base substitution A G upstream_gene_variant PRAD-UK 10 1182514 1182514 single base substitution T C downstream_gene_variant PRAD-UK 10 1182575 1182575 single base substitution T G downstream_gene_variant PRAD-US 10 1142152 1142152 single base substitution A G missense_variant Q198R 593A>G PRAD-US 10 1142152 1142152 single base substitution A G missense_variant Q231R 692A>G PRAD-US 10 1149689 1149689 deletion of <=200bp G - frameshift_variant G292 READ-US 10 1094906 1094906 single base substitution C T upstream_gene_variant READ-US 10 1130478 1130478 single base substitution G A missense_variant D145N 433G>A READ-US 10 1130478 1130478 single base substitution G A missense_variant D178N 532G>A RECA-EU 10 1094288 1094288 single base substitution C G upstream_gene_variant RECA-EU 10 1096088 1096088 single base substitution T A intron_variant RECA-EU 10 1100938 1100938 single base substitution T C intron_variant RECA-EU 10 1100938 1100938 single base substitution T C upstream_gene_variant RECA-EU 10 1100943 1100943 single base substitution G A intron_variant RECA-EU 10 1100943 1100943 single base substitution G A upstream_gene_variant RECA-EU 10 1111081 1111081 single base substitution A G intron_variant RECA-EU 10 1115641 1115641 single base substitution G A intron_variant RECA-EU 10 1115641 1115641 single base substitution G A upstream_gene_variant RECA-EU 10 1129795 1129795 single base substitution C T intron_variant RECA-EU 10 1141711 1141711 single base substitution G A intron_variant RECA-EU 10 1157036 1157036 single base substitution A C intron_variant RECA-EU 10 1157468 1157468 single base substitution T A intron_variant RECA-EU 10 1161592 1161592 single base substitution C G intron_variant RECA-EU 10 1166043 1166043 single base substitution C T intron_variant RECA-EU 10 1166043 1166043 single base substitution C T upstream_gene_variant RECA-EU 10 1175464 1175464 single base substitution T G 3_prime_UTR_variant RECA-EU 10 1175464 1175464 single base substitution T G downstream_gene_variant RECA-EU 10 1177657 1177657 single base substitution T C 3_prime_UTR_variant RECA-EU 10 1177657 1177657 single base substitution T C downstream_gene_variant RECA-EU 10 1178803 1178803 single base substitution G A downstream_gene_variant RECA-EU 10 1182389 1182389 single base substitution G C downstream_gene_variant SKCA-BR 10 1092512 1092512 single base substitution A C upstream_gene_variant SKCA-BR 10 1092527 1092527 single base substitution C T upstream_gene_variant SKCA-BR 10 1100960 1100960 single base substitution A C intron_variant SKCA-BR 10 1100960 1100960 single base substitution A C upstream_gene_variant SKCA-BR 10 1102386 1102386 single base substitution G A 5_prime_UTR_variant SKCA-BR 10 1102386 1102386 single base substitution G A intron_variant SKCA-BR 10 1102386 1102386 single base substitution G A upstream_gene_variant SKCA-BR 10 1103447 1103447 single base substitution C T intron_variant SKCA-BR 10 1104030 1104030 insertion of <=200bp - CACGGTATG intron_variant SKCA-BR 10 1107259 1107259 single base substitution T G intron_variant SKCA-BR 10 1107778 1107778 insertion of <=200bp - CA intron_variant SKCA-BR 10 1110523 1110538 deletion of <=200bp CTTTTTTTTTTTTTTT - intron_variant SKCA-BR 10 1118900 1118900 single base substitution C A intron_variant SKCA-BR 10 1118900 1118900 single base substitution C A upstream_gene_variant SKCA-BR 10 1121724 1121724 insertion of <=200bp - CT intron_variant SKCA-BR 10 1128352 1128352 single base substitution C T intron_variant SKCA-BR 10 1130103 1130103 single base substitution T G intron_variant SKCA-BR 10 1132848 1132848 single base substitution G C intron_variant SKCA-BR 10 1134114 1134114 single base substitution T G intron_variant SKCA-BR 10 1134452 1134452 single base substitution A T intron_variant SKCA-BR 10 1135582 1135608 deletion of <=200bp AGCCTTCCCGTGCTCACCCGCAGTTCG - intron_variant SKCA-BR 10 1135630 1135630 single base substitution G A intron_variant SKCA-BR 10 1135634 1135634 single base substitution G A intron_variant SKCA-BR 10 1135635 1135635 single base substitution G A intron_variant SKCA-BR 10 1137291 1137291 single base substitution C T intron_variant SKCA-BR 10 1139418 1139418 single base substitution G A missense_variant E178K 532G>A SKCA-BR 10 1139418 1139418 single base substitution G A missense_variant E211K 631G>A SKCA-BR 10 1145372 1145372 single base substitution C T downstream_gene_variant SKCA-BR 10 1145372 1145372 single base substitution C T intron_variant SKCA-BR 10 1145867 1145867 single base substitution C T downstream_gene_variant SKCA-BR 10 1145867 1145867 single base substitution C T intron_variant SKCA-BR 10 1145894 1145894 single base substitution A G downstream_gene_variant SKCA-BR 10 1145894 1145894 single base substitution A G intron_variant SKCA-BR 10 1147564 1147564 single base substitution C T downstream_gene_variant SKCA-BR 10 1147564 1147564 single base substitution C T intron_variant SKCA-BR 10 1148219 1148219 single base substitution C T intron_variant SKCA-BR 10 1148530 1148530 single base substitution C G intron_variant SKCA-BR 10 1149994 1149994 single base substitution C T intron_variant SKCA-BR 10 1152182 1152182 single base substitution C T intron_variant SKCA-BR 10 1152246 1152246 single base substitution C T intron_variant SKCA-BR 10 1152247 1152247 single base substitution C T intron_variant SKCA-BR 10 1156062 1156062 single base substitution T A intron_variant SKCA-BR 10 1156165 1156165 single base substitution T C intron_variant SKCA-BR 10 1157070 1157070 single base substitution C T intron_variant SKCA-BR 10 1158660 1158660 single base substitution A C intron_variant SKCA-BR 10 1159278 1159279 deletion of <=200bp CA - intron_variant SKCA-BR 10 1159280 1159280 single base substitution C T intron_variant SKCA-BR 10 1164372 1164372 single base substitution G A intron_variant SKCA-BR 10 1166687 1166687 single base substitution C G intron_variant SKCA-BR 10 1166687 1166687 single base substitution C G upstream_gene_variant SKCA-BR 10 1168285 1168285 single base substitution G T intron_variant SKCA-BR 10 1168285 1168285 single base substitution G T upstream_gene_variant SKCA-BR 10 1168292 1168292 single base substitution T C intron_variant SKCA-BR 10 1168292 1168292 single base substitution T C upstream_gene_variant SKCA-BR 10 1168343 1168343 single base substitution T G intron_variant SKCA-BR 10 1168343 1168343 single base substitution T G upstream_gene_variant SKCA-BR 10 1168722 1168722 single base substitution A C intron_variant SKCA-BR 10 1168722 1168722 single base substitution A C upstream_gene_variant SKCA-BR 10 1168828 1168828 single base substitution C T intron_variant SKCA-BR 10 1168828 1168828 single base substitution C T upstream_gene_variant SKCA-BR 10 1170597 1170607 deletion of <=200bp AGTGTGTGTGT - intron_variant SKCA-BR 10 1179829 1179829 single base substitution C T downstream_gene_variant SKCM-US 10 1126377 1126377 single base substitution C A synonymous_variant S119S 357C>A SKCM-US 10 1126377 1126377 single base substitution C A synonymous_variant S86S 258C>A SKCM-US 10 1149546 1149546 single base substitution C T missense_variant S244F 731C>T SKCM-US 10 1149760 1149760 single base substitution C T synonymous_variant L315L 945C>T SKCM-US 10 1175199 1175199 single base substitution C T downstream_gene_variant SKCM-US 10 1175199 1175199 single base substitution C T missense_variant P467L 1400C>T STAD-US 10 1118155 1118155 single base substitution C A synonymous_variant S20S 60C>A STAD-US 10 1118155 1118155 single base substitution C A upstream_gene_variant STAD-US 10 1126003 1126003 single base substitution G A synonymous_variant A63A 189G>A STAD-US 10 1126003 1126003 single base substitution G A synonymous_variant A96A 288G>A STAD-US 10 1126020 1126020 single base substitution T C missense_variant L102P 305T>C STAD-US 10 1126020 1126020 single base substitution T C missense_variant L69P 206T>C STAD-US 10 1149661 1149661 single base substitution C T synonymous_variant G282G 846C>T STAD-US 10 1151106 1151106 single base substitution C A synonymous_variant T334T 1002C>A STAD-US 10 1170870 1170870 deletion of <=200bp A - exon_variant STAD-US 10 1170870 1170870 deletion of <=200bp A - frameshift_variant Q420 STAD-US 10 1170951 1170951 single base substitution G A exon_variant STAD-US 10 1170951 1170951 single base substitution G A missense_variant R447Q 1340G>A THCA-SA 10 1149652 1149653 deletion of <=200bp CC - frameshift_variant SH279 UCEC-US 10 1118121 1118121 single base substitution C T missense_variant S9L 26C>T UCEC-US 10 1118121 1118121 single base substitution C T upstream_gene_variant UCEC-US 10 1123904 1123904 single base substitution G T stop_gained E33* 97G>T UCEC-US 10 1123904 1123904 single base substitution G T stop_gained E66* 196G>T UCEC-US 10 1123910 1123910 single base substitution G T stop_gained E35* 103G>T UCEC-US 10 1123910 1123910 single base substitution G T stop_gained E68* 202G>T UCEC-US 10 1123944 1123944 single base substitution G A splice_donor_variant UCEC-US 10 1130353 1130353 single base substitution G A missense_variant S103N 308G>A UCEC-US 10 1130353 1130353 single base substitution G A missense_variant S136N 407G>A UCEC-US 10 1149581 1149581 single base substitution G A missense_variant E256K 766G>A UCEC-US 10 1170271 1170271 single base substitution G A exon_variant UCEC-US 10 1170271 1170271 single base substitution G A missense_variant R406H 1217G>A UCEC-US 10 1175180 1175180 single base substitution G A exon_variant UCEC-US 10 1175180 1175180 single base substitution G A missense_variant A461T 1381G>A

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand Case4g COSM1717042 c.908G>A p.R303Q Substitution - Missense 10:1103783-1103783 + H384 COSM5043835 c.649+2T>C p.? Unknown 10:1093498-1093498 + TCGA-HU-A4G9-01 COSM4011538 c.60C>A p.S20S Substitution - coding silent 10:1072215-1072215 + Case4a COSM1717042 c.908G>A p.R303Q Substitution - Missense 10:1103783-1103783 + OSCC-GB_00920111 COSM4881744 c.476T>C p.I159T Substitution - Missense 10:1084482-1084482 + S02241 COSM5676715 c.1348C>T p.R450* Substitution - Nonsense 10:1125019-1125019 + 134398 COSM326874 c.1213A>G p.I405V Substitution - Missense 10:1124327-1124327 + AOCS-131-1-3 COSM3952807 c.993A>T p.T331T Substitution - coding silent 10:1105157-1105157 + Case4i COSM1717042 c.908G>A p.R303Q Substitution - Missense 10:1103783-1103783 + S00944 COSM316530 c.468G>T p.R156R Substitution - coding silent 10:1084474-1084474 + ACINAR13 COSM1732931 c.1373G>C p.C458S Substitution - Missense 10:1129232-1129232 + KM12 COSM1675018 c.1216C>T p.R406C Substitution - Missense 10:1124330-1124330 + TCGA-DD-A73G-01 COSM4941337 c.908G>T p.R303L Substitution - Missense 10:1103783-1103783 + TCGA-29-1699-01 COSM1321521 c.1239-1G>A p.? Unknown 10:1124909-1124909 + TCGA-EK-A3GK-01 COSM4853411 c.622C>T p.H208Y Substitution - Missense 10:1093469-1093469 + LC_C9 COSM1187878 c.857C>T p.A286V Substitution - Missense 10:1103732-1103732 + TARGET-30-PARVLK COSM1288937 c.1321C>G p.R441G Substitution - Missense 10:1124992-1124992 + 8 COSM4166769 c.420G>A p.T140T Substitution - coding silent 10:1084426-1084426 + TCGA-BR-7851-01 COSM4011671 c.846C>T p.G282G Substitution - coding silent 10:1103721-1103721 + TCGA-A2-A0T5-01 COSM3806508 c.1417A>C p.T473P Substitution - Missense 10:1129276-1129276 + SK00102_M COSM1599988 c.814G>A p.V272I Substitution - Missense 10:1103689-1103689 + RK091_C01 COSM1627317 c.1072C>A p.H358N Substitution - Missense 10:1105236-1105236 + Case4c COSM1717042 c.908G>A p.R303Q Substitution - Missense 10:1103783-1103783 + S00944 COSM316530 c.468G>T p.R156R Substitution - coding silent 10:1084474-1084474 + TCGA-AF-2687-01 COSM1560977 c.532G>A p.D178N Substitution - Missense 10:1084538-1084538 + SM-4B296 COSM4409603 c.698C>T p.P233L Substitution - Missense 10:1096218-1096218 + 8016470 COSM3382674 c.1042C>T p.R348C Substitution - Missense 10:1105206-1105206 + TCGA-AP-A056-01 COSM914883 c.766G>A p.E256K Substitution - Missense 10:1103641-1103641 + TCGA-D5-6930-01 COSM915101 c.1217G>A p.R406H Substitution - Missense 10:1124331-1124331 + CSCC-41-T COSM4458532 c.1089C>T p.F363F Substitution - coding silent 10:1105253-1105253 + BD57T COSM3382674 c.1042C>T p.R348C Substitution - Missense 10:1105206-1105206 + TCGA-BR-6802-01 COSM1345942 c.1340G>A p.R447Q Substitution - Missense 10:1125011-1125011 + TCGA-A2-A0T5-01 COSM3806457 c.702A>C p.T234T Substitution - coding silent 10:1096222-1096222 + TCGA-BS-A0UF-01 COSM914749 c.196G>T p.E66* Substitution - Nonsense 10:1077964-1077964 + S00836 COSM316527 c.1008G>A p.R336R Substitution - coding silent 10:1105172-1105172 + HCC30T COSM3665497 c.659A>T p.D220V Substitution - Missense 10:1096179-1096179 + Case4j COSM1717042 c.908G>A p.R303Q Substitution - Missense 10:1103783-1103783 + RK194_C01 COSM1627309 c.397-3C>T p.? Unknown 10:1084400-1084400 + CSCC-31-T COSM4562133 c.913G>A p.A305T Substitution - Missense 10:1103788-1103788 + TCGA-AP-A056-01 COSM915101 c.1217G>A p.R406H Substitution - Missense 10:1124331-1124331 + PT46 COSM1627309 c.397-3C>T p.? Unknown 10:1084400-1084400 + TCGA-BR-8487-01 COSM4011678 c.1002C>A p.T334T Substitution - coding silent 10:1105166-1105166 + TCGA-CG-5723-01 COSM4011587 c.305T>C p.L102P Substitution - Missense 10:1080080-1080080 + PD13165a COSM5773279 c.407G>T p.S136I Substitution - Missense 10:1084413-1084413 + TCGA-AO-A03N-01 COSM427066 c.107C>T p.T36M Substitution - Missense 10:1072262-1072262 + TCGA-BR-8680-01 COSM4011585 c.288G>A p.A96A Substitution - coding silent 10:1080063-1080063 + 8068563 COSM4388140 c.76C>T p.R26* Substitution - Nonsense 10:1072231-1072231 + ESCC-078T COSM3934934 c.1125C>A p.F375L Substitution - Missense 10:1124239-1124239 + TCGA-B0-5107-01 COSM465273 c.960A>C p.T320T Substitution - coding silent 10:1103835-1103835 + ESO-167 COSM1270394 c.43A>C p.K15Q Substitution - Missense 10:1072198-1072198 + SS6003314 COSM4055022 c.561G>A p.E187E Substitution - coding silent 10:1086314-1086314 + T29 COSM5618332 c.1186A>G p.K396E Substitution - Missense 10:1124300-1124300 + TCGA-EB-A41A-01 COSM3434181 c.945C>T p.L315L Substitution - coding silent 10:1103820-1103820 + OSCC-GB_00560111 COSM4883624 c.1349G>T p.R450L Substitution - Missense 10:1125020-1125020 + DN111AA COSM5773279 c.407G>T p.S136I Substitution - Missense 10:1084413-1084413 + TCGA-30-1718-01 COSM1321533 c.703C>A p.P235T Substitution - Missense 10:1096223-1096223 + CSCC-31-T COSM4518837 c.827_828CC>TT p.S276F Substitution - Missense 10:1103702-1103703 + ME048T COSM229764 c.533-2A>C p.? Unknown 10:1086284-1086284 + Case4b COSM1717042 c.908G>A p.R303Q Substitution - Missense 10:1103783-1103783 + SNUH_G16_S1 COSM3997748 c.229T>A p.L77I Substitution - Missense 10:1077997-1077997 + T3 COSM5619196 c.354C>T p.L118L Substitution - coding silent 10:1080434-1080434 + S00936 COSM316529 c.856G>A p.A286T Substitution - Missense 10:1103731-1103731 + SNU-C4 COSM4651746 c.266G>A p.R89H Substitution - Missense 10:1080041-1080041 + TCGA-HU-A4GT-01 COSM1345942 c.1340G>A p.R447Q Substitution - Missense 10:1125011-1125011 + T96 COSM238433 c.1140C>T p.N380N Substitution - coding silent 10:1124254-1124254 + 469 COSM4437518 c.1458C>T p.N486N Substitution - coding silent 10:1129317-1129317 + Case4h COSM1717042 c.908G>A p.R303Q Substitution - Missense 10:1103783-1103783 + HCC50 COSM1602988 c.744A>G p.E248E Substitution - coding silent 10:1103619-1103619 + TCGA-BH-A0WA-01 COSM427073 c.175C>T p.L59L Substitution - coding silent 10:1077943-1077943 + TCGA-FW-A3R5-06 COSM3866514 c.731C>T p.S244F Substitution - Missense 10:1103606-1103606 + TCGA-A6-6653-01 COSM1345942 c.1340G>A p.R447Q Substitution - Missense 10:1125011-1125011 + TCGA-A5-A0GH-01 COSM915119 c.1381G>A p.A461T Substitution - Missense 10:1129240-1129240 + TCGA-HC-7212-01 COSM3782513 c.692A>G p.Q231R Substitution - Missense 10:1096212-1096212 + PT49 COSM5935655 c.236-5C>T p.? Unknown 10:1080006-1080006 + CSCC-27-T COSM4484004 c.275C>T p.A92V Substitution - Missense 10:1080050-1080050 + TCGA-DU-7304-01 COSM3966900 c.1346G>T p.S449I Substitution - Missense 10:1125017-1125017 + LUAD-S01356 COSM397919 c.844_845GG>TT p.G282>? Complex 10:1103719-1103720 + PD9702a COSM5772673 c.649+5G>A p.? Unknown 10:1093501-1093501 + CSCC-16-T COSM1345803 c.847G>A p.V283M Substitution - Missense 10:1103722-1103722 + T263 COSM1717042 c.908G>A p.R303Q Substitution - Missense 10:1103783-1103783 + sysucc-1370T COSM5469355 c.862G>A p.D288N Substitution - Missense 10:1103737-1103737 + Case4e COSM1717042 c.908G>A p.R303Q Substitution - Missense 10:1103783-1103783 + I2L-P10-Tumor-Organoid COSM5359820 c.223G>A p.E75K Substitution - Missense 10:1077991-1077991 + TCGA-D1-A16F-01 COSM914751 c.235+1G>A p.? Unknown 10:1078004-1078004 + TCGA-BS-A0UV-01 COSM914699 c.26C>T p.S9L Substitution - Missense 10:1072181-1072181 + KM12 COSM1675018 c.1216C>T p.R406C Substitution - Missense 10:1124330-1124330 + TCGA-EK-A2RA-01 COSM4848338 c.675C>T p.I225I Substitution - coding silent 10:1096195-1096195 + Case4d COSM1717042 c.908G>A p.R303Q Substitution - Missense 10:1103783-1103783 + T2284 COSM4166769 c.420G>A p.T140T Substitution - coding silent 10:1084426-1084426 + TCGA-EE-A29D-06 COSM3434441 c.1400C>T p.P467L Substitution - Missense 10:1129259-1129259 + TCGA-EB-A5UL-06 COSM3434441 c.1400C>T p.P467L Substitution - Missense 10:1129259-1129259 + Case4f COSM1717042 c.908G>A p.R303Q Substitution - Missense 10:1103783-1103783 + HCC50T COSM1602988 c.744A>G p.E248E Substitution - coding silent 10:1103619-1103619 + TCGA-D8-A1XK-01 COSM3806463 c.888T>G p.A296A Substitution - coding silent 10:1103763-1103763 + TCGA-A5-A0GP-01 COSM914750 c.202G>T p.E68* Substitution - Nonsense 10:1077970-1077970 + S00936 COSM316528 c.287C>T p.A96V Substitution - Missense 10:1080062-1080062 + TCGA-EJ-5506-01 COSM1128137 c.1066T>C p.S356P Substitution - Missense 10:1105230-1105230 + CS02 COSM4967320 c.782G>T p.G261V Substitution - Missense 10:1103657-1103657 + ESO-0292 COSM1241896 c.906C>T p.D302D Substitution - coding silent 10:1103781-1103781 + TCGA-D1-A163-01 COSM914803 c.407G>A p.S136N Substitution - Missense 10:1084413-1084413 + PTC_285 COSM5958729 c.837_838delCC p.S279fs*65 Deletion - Frameshift 10:1103712-1103713 + TCGA-GF-A6C8-06 COSM3866488 c.357C>A p.S119S Substitution - coding silent 10:1080437-1080437 + HCC30 COSM3665497 c.659A>T p.D220V Substitution - Missense 10:1096179-1096179 + TCGA-A6-6781-01 COSM1345803 c.847G>A p.V283M Substitution - Missense 10:1103722-1103722 + TCGA-23-2649-01 COSM1321523 c.1204A>G p.I402V Substitution - Missense 10:1124318-1124318 + DLD1 COSM4621773 c.401T>C p.V134A Substitution - Missense 10:1084407-1084407 + ICGC_MB127 COSM3764235 c.1353+10C>T p.? Unknown 10:1125034-1125034 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.188491;Hs.188495 10p15.3 2427736|CGAP|BC018044|A/G|non-coding||43|Validated; 1230602|dbSNP|BC018044|A/G|non-coding||1296|Candidate; 2430890|dbSNP|BC018044|A/G|non-coding||1296|Validated

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.D354A c.1061A>C 10 1151165 LUAD A C Missense p.K15Q c.43A>C 10 1118138 ESCA A C Synonymous p.T320T c.960A>C 10 1149775 RCCC A G Missense p.I405V c.1213A>G 10 1170267 SCLC A G Missense p.Q231R c.692A>G 10 1142152 PRAD C G Missense p.Q64E c.190C>G 10 1123898 HNSC C G Missense p.R441G c.1321C>G 10 1170932 NB C G Missense p.T340S c.1019C>G 10 1151123 BRCA C G Synonymous p.L107L c.321C>G 10 1126036 LUAD C T Missense p.A96V c.287C>T 10 1126002 SCLC C T Missense p.P467L c.1400C>T 10 1175199 CM C T Missense p.T36M c.107C>T 10 1118202 BRCA C T Synonymous p.L59L c.175C>T 10 1123883 BRCA G A Missense p.A286T c.856G>A 10 1149671 SCLC G A Missense p.A461T c.1381G>A 10 1175180 UCEC G A Missense p.D157N c.469G>A 10 1130415 CM G A Missense p.R399K c.1196G>A 10 1170250 CM G A Missense p.R447Q c.1340G>A 10 1170951 STAD G A Missense p.S136N c.407G>A 10 1130353 UCEC G A SpliceDonorSNV . c.235+1G>A 10 1123944 UCEC G A Synonymous p.R336R c.1008G>A 10 1151112 SCLC G A Synonymous p.T327T c.981G>A 10 1151085 STAD G T Missense p.R478L c.1433G>T 10 1175232 CM G T Missense p.S449I c.1346G>T 10 1170957 LGG G T Missense p.V390L c.1168G>T 10 1170222 LUAD G T Nonsense p.E68* c.202G>T 10 1123910 UCEC G T Synonymous p.R156R c.468G>T 10 1130414 SCLC T C Missense p.F375L c.1123T>C 10 1170177 STAD T C Missense p.S356P c.1066T>C 10 1151170 BRCA