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 10 93024204 93024204 + Missense_Mutation SNP A A G TCGA-OR-A5JW-01A-11D-A29I-10 TCGA-OR-A5JW-10A-01D-A29L-10 g.chr10:93024204A>G c.590A>G c.(589-591)aAt>aGt p.N197S BRCA 10 93011092 93011092 + Silent SNP T T G TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr10:93011092T>G c.369T>G c.(367-369)ggT>ggG p.G123G BRCA 10 93011102 93011102 + Missense_Mutation SNP G G A TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr10:93011102G>A c.379G>A c.(379-381)Gaa>Aaa p.E127K BRCA 10 93021117 93021117 + Missense_Mutation SNP G G A TCGA-E2-A15R-01A-11D-A10Y-09 TCGA-E2-A15R-10A-01D-A110-09 g.chr10:93021117G>A c.509G>A c.(508-510)cGt>cAt p.R170H CESC 10 93011180 93011180 + Missense_Mutation SNP G G A TCGA-JW-A5VG-01A-11D-A28B-09 TCGA-JW-A5VG-10A-01D-A28E-09 g.chr10:93011180G>A c.457G>A c.(457-459)Ggg>Agg p.G153R CESC 10 93021139 93021139 + Missense_Mutation SNP A A C TCGA-FU-A3HZ-01A-11D-A20U-09 TCGA-FU-A3HZ-10A-01D-A20U-09 g.chr10:93021139A>C c.531A>C c.(529-531)aaA>aaC p.K177N CHOL 10 93021177 93021177 + Missense_Mutation SNP A A G TCGA-W5-AA39-01A-11D-A417-09 TCGA-W5-AA39-10A-01D-A41A-09 g.chr10:93021177A>G c.569A>G c.(568-570)tAt>tGt p.Y190C COAD 10 93011047 93011047 + Splice_Site SNP A A G TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr10:93011047A>G c.e6-1 COAD 10 93011118 93011118 + Missense_Mutation SNP A A G TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr10:93011118A>G c.395A>G c.(394-396)tAt>tGt p.Y132C COAD 10 93011160 93011160 + Missense_Mutation SNP T T C TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr10:93011160T>C c.437T>C c.(436-438)tTa>tCa p.L146S COAD 10 93021144 93021144 + Missense_Mutation SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:93021144T>G c.536T>G c.(535-537)tTt>tGt p.F179C COAD 10 93031399 93031399 + Missense_Mutation SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:93031399G>A c.668G>A c.(667-669)cGg>cAg p.R223Q COADREAD 10 93011047 93011047 + Splice_Site SNP A A G TCGA-A6-5661-01A-01D-1650-10 TCGA-A6-5661-10A-01D-1650-10 g.chr10:93011047A>G c.e6-1 COADREAD 10 93011118 93011118 + Missense_Mutation SNP A A G TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr10:93011118A>G c.395A>G c.(394-396)tAt>tGt p.Y132C COADREAD 10 93011160 93011160 + Missense_Mutation SNP T T C TCGA-AA-3672-01A-01W-0900-09 TCGA-AA-3672-10A-01W-0900-09 g.chr10:93011160T>C c.437T>C c.(436-438)tTa>tCa p.L146S COADREAD 10 93021137 93021137 + Frame_Shift_Del DEL A A - TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr10:93021137delA c.529delA c.(529-531)aaafs p.K178fs COADREAD 10 93021144 93021144 + Missense_Mutation SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:93021144T>G c.536T>G c.(535-537)tTt>tGt p.F179C COADREAD 10 93031399 93031399 + Missense_Mutation SNP G G A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:93031399G>A c.668G>A c.(667-669)cGg>cAg p.R223Q ESCA 10 92982738 92982738 + Missense_Mutation SNP C C T TCGA-S8-A6BV-01A-21D-A31U-09 TCGA-S8-A6BV-10A-01D-A31U-09 g.chr10:92982738C>T c.110C>T c.(109-111)aCa>aTa p.T37I GBM 10 93038067 93038067 + Silent SNP C C T TCGA-14-2554-01A-01D-1494-08 TCGA-14-2554-10A-01D-1494-08 g.chr10:93038067C>T c.765C>T c.(763-765)ttC>ttT p.F255F GBMLGG 10 93008278 93008278 + Nonsense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:93008278G>T c.226G>T c.(226-228)Gag>Tag p.E76* GBMLGG 10 93008308 93008308 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:93008308C>T c.256C>T c.(256-258)Cta>Tta p.L86L GBMLGG 10 93038067 93038067 + Silent SNP C C T TCGA-14-2554-01A-01D-1494-08 TCGA-14-2554-10A-01D-1494-08 g.chr10:93038067C>T c.765C>T c.(763-765)ttC>ttT p.F255F HNSC 10 93011162 93011162 + Missense_Mutation SNP C C G TCGA-CR-7398-01A-11D-2012-08 TCGA-CR-7398-10A-01D-2013-08 g.chr10:93011162C>G c.439C>G c.(439-441)Cga>Gga p.R147G HNSC 10 93038049 93038049 + Nonsense_Mutation SNP T T G TCGA-BA-7269-01A-11D-2012-08 TCGA-BA-7269-10A-01D-2013-08 g.chr10:93038049T>G c.747T>G c.(745-747)taT>taG p.Y249* LGG 10 93008278 93008278 + Nonsense_Mutation SNP G G T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:93008278G>T c.226G>T c.(226-228)Gag>Tag p.E76* LGG 10 93008308 93008308 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:93008308C>T c.256C>T c.(256-258)Cta>Tta p.L86L LIHC 10 93000241 93000241 + Splice_Site SNP T T C TCGA-DD-A39Y-01A-11D-A20W-10 TCGA-DD-A39Y-11A-11D-A20W-10 g.chr10:93000241T>C c.113T>C c.(112-114)tTc>tCc p.F38S LIHC 10 93021180 93021180 + Splice_Site SNP A A G TCGA-DD-A39X-01A-11D-A20W-10 TCGA-DD-A39X-11A-11D-A20W-10 g.chr10:93021180A>G c.572A>G c.(571-573)gAg>gGg p.E191G LUAD 10 92982639 92982639 + Missense_Mutation SNP A A T TCGA-91-8497-01A-11D-2393-08 TCGA-91-8497-10A-01D-2393-08 g.chr10:92982639A>T c.11A>T c.(10-12)cAa>cTa p.Q4L LUAD 10 93000258 93000258 + Missense_Mutation SNP G G T TCGA-44-6778-01A-11D-1855-08 TCGA-44-6778-10A-01D-1855-08 g.chr10:93000258G>T c.130G>T c.(130-132)Gtt>Ttt p.V44F LUAD 10 93011157 93011157 + Missense_Mutation SNP G G A TCGA-05-4410-01A-21D-1855-08 TCGA-05-4410-10A-01D-1855-08 g.chr10:93011157G>A c.434G>A c.(433-435)tGt>tAt p.C145Y LUSC 10 93008287 93008287 + Missense_Mutation SNP A A G TCGA-34-5231-01A-21D-1817-08 TCGA-34-5231-10A-01D-1817-08 g.chr10:93008287A>G c.235A>G c.(235-237)Ata>Gta p.I79V PAAD 10 93011074 93011074 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr10:93011074G>A c.351G>A c.(349-351)ccG>ccA p.P117P PAAD 10 93011174 93011174 + Nonsense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr10:93011174C>T c.451C>T c.(451-453)Caa>Taa p.Q151* READ 10 93021137 93021137 + Frame_Shift_Del DEL A A - TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr10:93021137delA c.529delA c.(529-531)aaafs p.K178fs SKCM 10 92982654 92982654 + Missense_Mutation SNP T T G TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr10:92982654T>G c.26T>G c.(25-27)gTg>gGg p.V9G SKCM 10 93000322 93000322 + Missense_Mutation SNP C C T TCGA-FS-A4F5-06A-11D-A25O-08 TCGA-FS-A4F5-10B-01D-A25O-08 g.chr10:93000322C>T c.194C>T c.(193-195)cCa>cTa p.P65L

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 92977186 92977186 single base substitution A G upstream_gene_variant BRCA-EU 10 92978626 92978626 single base substitution C G upstream_gene_variant BRCA-EU 10 92979625 92979625 single base substitution A G upstream_gene_variant BRCA-EU 10 92983264 92983264 single base substitution G T downstream_gene_variant BRCA-EU 10 92983264 92983264 single base substitution G T intron_variant BRCA-EU 10 92983389 92983389 single base substitution G T downstream_gene_variant BRCA-EU 10 92983389 92983389 single base substitution G T intron_variant BRCA-EU 10 92984215 92984215 single base substitution T G downstream_gene_variant BRCA-EU 10 92984215 92984215 single base substitution T G intron_variant BRCA-EU 10 92985259 92985259 single base substitution A G downstream_gene_variant BRCA-EU 10 92985259 92985259 single base substitution A G intron_variant BRCA-EU 10 92988213 92988213 single base substitution C G downstream_gene_variant BRCA-EU 10 92988213 92988213 single base substitution C G intron_variant BRCA-EU 10 92990128 92990128 single base substitution T A downstream_gene_variant BRCA-EU 10 92990128 92990128 single base substitution T A intron_variant BRCA-EU 10 92991116 92991116 single base substitution G C downstream_gene_variant BRCA-EU 10 92991116 92991116 single base substitution G C intron_variant BRCA-EU 10 92991661 92991661 single base substitution G T downstream_gene_variant BRCA-EU 10 92991661 92991661 single base substitution G T intron_variant BRCA-EU 10 92991873 92991873 single base substitution C A downstream_gene_variant BRCA-EU 10 92991873 92991873 single base substitution C A intron_variant BRCA-EU 10 92993768 92993768 single base substitution A T intron_variant BRCA-EU 10 92995973 92995973 single base substitution G T intron_variant BRCA-EU 10 92996226 92996226 single base substitution G A intron_variant BRCA-EU 10 92999040 92999040 single base substitution T A intron_variant BRCA-EU 10 92999127 92999127 single base substitution G T intron_variant BRCA-EU 10 93000800 93000800 insertion of <=200bp - AT intron_variant BRCA-EU 10 93003448 93003448 single base substitution C T intron_variant BRCA-EU 10 93004151 93004151 single base substitution G A intron_variant BRCA-EU 10 93004345 93004345 single base substitution G C intron_variant BRCA-EU 10 93005247 93005247 deletion of <=200bp G - intron_variant BRCA-EU 10 93006431 93006431 single base substitution G C intron_variant BRCA-EU 10 93006871 93006871 single base substitution G A intron_variant BRCA-EU 10 93007206 93007206 single base substitution G C intron_variant BRCA-EU 10 93007226 93007226 single base substitution G C intron_variant BRCA-EU 10 93008311 93008311 single base substitution C T stop_gained R87* 259C>T BRCA-EU 10 93011329 93011329 single base substitution A G intron_variant BRCA-EU 10 93011796 93011796 single base substitution G C intron_variant BRCA-EU 10 93012414 93012414 single base substitution G T intron_variant BRCA-EU 10 93013092 93013092 single base substitution C G intron_variant BRCA-EU 10 93016181 93016181 single base substitution G A intron_variant BRCA-EU 10 93017347 93017347 single base substitution G A intron_variant BRCA-EU 10 93023776 93023776 single base substitution T A intron_variant BRCA-EU 10 93024148 93024148 single base substitution C T intron_variant BRCA-EU 10 93026709 93026709 single base substitution C A intron_variant BRCA-EU 10 93028244 93028244 single base substitution C T intron_variant BRCA-EU 10 93028649 93028649 single base substitution C G intron_variant BRCA-EU 10 93030643 93030643 single base substitution G C intron_variant BRCA-EU 10 93030863 93030863 insertion of <=200bp - ATATATATATAATCTA intron_variant BRCA-EU 10 93033748 93033748 single base substitution G A intron_variant BRCA-EU 10 93034361 93034361 deletion of <=200bp A - intron_variant BRCA-EU 10 93035772 93035772 single base substitution C T intron_variant BRCA-EU 10 93036189 93036189 single base substitution G C intron_variant BRCA-EU 10 93037089 93037089 single base substitution G C intron_variant BRCA-EU 10 93040306 93040306 single base substitution C G 3_prime_UTR_variant BRCA-EU 10 93040306 93040306 single base substitution C G downstream_gene_variant BRCA-EU 10 93042157 93042157 single base substitution C G 3_prime_UTR_variant BRCA-EU 10 93042157 93042157 single base substitution C G downstream_gene_variant BRCA-EU 10 93043251 93043251 single base substitution G C 3_prime_UTR_variant BRCA-EU 10 93043251 93043251 single base substitution G C downstream_gene_variant BRCA-EU 10 93043273 93043273 single base substitution G C 3_prime_UTR_variant BRCA-EU 10 93043273 93043273 single base substitution G C downstream_gene_variant BRCA-EU 10 93043528 93043528 single base substitution G A 3_prime_UTR_variant BRCA-EU 10 93043620 93043620 single base substitution C G 3_prime_UTR_variant BRCA-EU 10 93043802 93043802 single base substitution C G 3_prime_UTR_variant BRCA-EU 10 93044659 93044659 single base substitution G C downstream_gene_variant BRCA-EU 10 93047324 93047324 single base substitution G T downstream_gene_variant BRCA-EU 10 93047562 93047562 single base substitution C T downstream_gene_variant BRCA-EU 10 93047705 93047705 single base substitution T C downstream_gene_variant BRCA-EU 10 93047707 93047707 single base substitution G C downstream_gene_variant BRCA-EU 10 93047937 93047937 single base substitution G A downstream_gene_variant BRCA-EU 10 93048383 93048383 single base substitution A G downstream_gene_variant BRCA-EU 10 93048522 93048522 deletion of <=200bp A - downstream_gene_variant BRCA-FR 10 92984215 92984215 single base substitution T G downstream_gene_variant BRCA-FR 10 92984215 92984215 single base substitution T G intron_variant BRCA-FR 10 92999127 92999127 single base substitution G T intron_variant BRCA-FR 10 93003448 93003448 single base substitution C T intron_variant BRCA-FR 10 93013092 93013092 single base substitution C G intron_variant BRCA-FR 10 93018502 93018502 single base substitution A T intron_variant BRCA-UK 10 92988213 92988213 single base substitution C G downstream_gene_variant BRCA-UK 10 92988213 92988213 single base substitution C G intron_variant BRCA-US 10 93011092 93011092 single base substitution T G synonymous_variant G123G 369T>G BRCA-US 10 93011102 93011102 single base substitution G A missense_variant E127K 379G>A BRCA-US 10 93021117 93021117 single base substitution G A missense_variant R170H 509G>A BTCA-JP 10 93021100 93021100 single base substitution C A missense_variant F164L 492C>A CESC-US 10 93011180 93011180 single base substitution G A missense_variant G153R 457G>A CESC-US 10 93021139 93021139 single base substitution A C missense_variant K177N 531A>C CLLE-ES 10 92976171 92976171 single base substitution A G upstream_gene_variant CLLE-ES 10 93000667 93000670 deletion of <=200bp AGAA - intron_variant CLLE-ES 10 93011777 93011777 single base substitution C T intron_variant CLLE-ES 10 93023060 93023060 single base substitution T G intron_variant CLLE-ES 10 93033767 93033767 insertion of <=200bp - AT intron_variant COAD-US 10 93011118 93011118 single base substitution A G missense_variant Y132C 395A>G COAD-US 10 93021144 93021144 single base substitution T G missense_variant F179C 536T>G COAD-US 10 93031399 93031399 single base substitution G A missense_variant R223Q 668G>A COAD-US 10 93038067 93038067 single base substitution C T synonymous_variant F255F 765C>T COCA-CN 10 92979955 92979955 single base substitution A G 5_prime_UTR_variant COCA-CN 10 92979955 92979955 single base substitution A G exon_variant COCA-CN 10 92979955 92979955 single base substitution A G upstream_gene_variant COCA-CN 10 92996693 92996693 single base substitution A G intron_variant COCA-CN 10 93006734 93006734 single base substitution A G intron_variant COCA-CN 10 93013418 93013418 single base substitution C T intron_variant COCA-CN 10 93019952 93019952 single base substitution C T intron_variant COCA-CN 10 93024260 93024260 single base substitution C T stop_gained R216* 646C>T COCA-CN 10 93038067 93038067 single base substitution C T synonymous_variant F255F 765C>T ESAD-UK 10 92975817 92975817 single base substitution T C upstream_gene_variant ESAD-UK 10 92976120 92976120 single base substitution G C upstream_gene_variant ESAD-UK 10 92977168 92977168 single base substitution T A upstream_gene_variant ESAD-UK 10 92978241 92978241 single base substitution A C upstream_gene_variant ESAD-UK 10 92978335 92978335 single base substitution A C upstream_gene_variant ESAD-UK 10 92979855 92979855 single base substitution G C upstream_gene_variant ESAD-UK 10 92980929 92980929 single base substitution G A intron_variant ESAD-UK 10 92981718 92981719 deletion of <=200bp AG - intron_variant ESAD-UK 10 92984621 92984621 single base substitution C A downstream_gene_variant ESAD-UK 10 92984621 92984621 single base substitution C A intron_variant ESAD-UK 10 92991760 92991760 single base substitution A G downstream_gene_variant ESAD-UK 10 92991760 92991760 single base substitution A G intron_variant ESAD-UK 10 92991875 92991875 single base substitution T C downstream_gene_variant ESAD-UK 10 92991875 92991875 single base substitution T C intron_variant ESAD-UK 10 92995153 92995153 single base substitution A C intron_variant ESAD-UK 10 92995859 92995859 single base substitution A T intron_variant ESAD-UK 10 92998441 92998441 single base substitution A G intron_variant ESAD-UK 10 92998931 92998934 deletion of <=200bp TTGT - intron_variant ESAD-UK 10 93000073 93000073 single base substitution G A intron_variant ESAD-UK 10 93000818 93000818 single base substitution T C intron_variant ESAD-UK 10 93001107 93001107 single base substitution G C intron_variant ESAD-UK 10 93001638 93001638 single base substitution G T intron_variant ESAD-UK 10 93002188 93002188 single base substitution A C intron_variant ESAD-UK 10 93002918 93002918 single base substitution G A intron_variant ESAD-UK 10 93007260 93007260 single base substitution T G intron_variant ESAD-UK 10 93013940 93013940 single base substitution C G intron_variant ESAD-UK 10 93018568 93018568 single base substitution T C intron_variant ESAD-UK 10 93018755 93018755 single base substitution T C intron_variant ESAD-UK 10 93023085 93023085 single base substitution A T intron_variant ESAD-UK 10 93023634 93023634 single base substitution A C intron_variant ESAD-UK 10 93025154 93025154 single base substitution T G intron_variant ESAD-UK 10 93025352 93025352 single base substitution A C intron_variant ESAD-UK 10 93025840 93025840 single base substitution G A intron_variant ESAD-UK 10 93026224 93026224 deletion of <=200bp T - intron_variant ESAD-UK 10 93026286 93026286 single base substitution T C intron_variant ESAD-UK 10 93026398 93026398 deletion of <=200bp T - intron_variant ESAD-UK 10 93027610 93027610 single base substitution G A intron_variant ESAD-UK 10 93030860 93030860 insertion of <=200bp - TA intron_variant ESAD-UK 10 93032520 93032520 single base substitution A T intron_variant ESAD-UK 10 93037575 93037575 single base substitution C T intron_variant ESAD-UK 10 93037709 93037709 single base substitution G A intron_variant ESAD-UK 10 93037936 93037936 single base substitution A G intron_variant ESAD-UK 10 93038589 93038589 deletion of <=200bp A - 3_prime_UTR_variant ESAD-UK 10 93038589 93038589 deletion of <=200bp A - downstream_gene_variant ESAD-UK 10 93039594 93039594 single base substitution T A 3_prime_UTR_variant ESAD-UK 10 93039594 93039594 single base substitution T A downstream_gene_variant ESAD-UK 10 93039904 93039904 single base substitution C T 3_prime_UTR_variant ESAD-UK 10 93039904 93039904 single base substitution C T downstream_gene_variant ESAD-UK 10 93040695 93040695 single base substitution C T 3_prime_UTR_variant ESAD-UK 10 93040695 93040695 single base substitution C T downstream_gene_variant ESAD-UK 10 93043860 93043860 single base substitution C G 3_prime_UTR_variant ESAD-UK 10 93045360 93045360 single base substitution C G downstream_gene_variant ESAD-UK 10 93048762 93048762 single base substitution T G downstream_gene_variant GBM-US 10 93038067 93038067 single base substitution C T synonymous_variant F255F 765C>T LICA-FR 10 92986047 92986047 insertion of <=200bp - A downstream_gene_variant LICA-FR 10 92986047 92986047 insertion of <=200bp - A intron_variant LICA-FR 10 92991666 92991666 single base substitution T C downstream_gene_variant LICA-FR 10 92991666 92991666 single base substitution T C intron_variant LICA-FR 10 93010255 93010255 deletion of <=200bp T - intron_variant LICA-FR 10 93043075 93043075 single base substitution A G 3_prime_UTR_variant LICA-FR 10 93043075 93043075 single base substitution A G downstream_gene_variant LINC-JP 10 92979944 92979944 single base substitution A G 5_prime_UTR_variant LINC-JP 10 92979944 92979944 single base substitution A G exon_variant LINC-JP 10 92979944 92979944 single base substitution A G upstream_gene_variant LINC-JP 10 92981025 92981025 single base substitution C A intron_variant LINC-JP 10 92982593 92982593 single base substitution G C 5_prime_UTR_variant LINC-JP 10 92982593 92982593 single base substitution G C exon_variant LINC-JP 10 92987100 92987100 single base substitution A G downstream_gene_variant LINC-JP 10 92987100 92987100 single base substitution A G exon_variant LINC-JP 10 92987100 92987100 single base substitution A G intron_variant LINC-JP 10 92987100 92987100 single base substitution A G missense_variant E40G 119A>G LINC-JP 10 92987207 92987207 single base substitution C T downstream_gene_variant LINC-JP 10 92987207 92987207 single base substitution C T exon_variant LINC-JP 10 92987207 92987207 single base substitution C T intron_variant LINC-JP 10 93039088 93039088 single base substitution A T 3_prime_UTR_variant LINC-JP 10 93039088 93039088 single base substitution A T downstream_gene_variant LINC-JP 10 93039790 93039790 single base substitution T A 3_prime_UTR_variant LINC-JP 10 93039790 93039790 single base substitution T A downstream_gene_variant LINC-JP 10 93040103 93040103 single base substitution C T 3_prime_UTR_variant LINC-JP 10 93040103 93040103 single base substitution C T downstream_gene_variant LIRI-JP 10 92975157 92975157 single base substitution A C upstream_gene_variant LIRI-JP 10 92975347 92975347 single base substitution G A upstream_gene_variant LIRI-JP 10 92976498 92976498 single base substitution T C upstream_gene_variant LIRI-JP 10 92976770 92976770 single base substitution A G upstream_gene_variant LIRI-JP 10 92978804 92978804 single base substitution G T upstream_gene_variant LIRI-JP 10 92978847 92978847 single base substitution C A upstream_gene_variant LIRI-JP 10 92981554 92981554 single base substitution T A intron_variant LIRI-JP 10 92982740 92982740 single base substitution T A downstream_gene_variant LIRI-JP 10 92982740 92982740 single base substitution T A missense_variant F38I 112T>A LIRI-JP 10 92982740 92982740 single base substitution T A missense_variant S38T 112T>A LIRI-JP 10 92982740 92982740 single base substitution T A splice_region_variant LIRI-JP 10 92983282 92983282 single base substitution A G downstream_gene_variant LIRI-JP 10 92983282 92983282 single base substitution A G intron_variant LIRI-JP 10 92984062 92984062 single base substitution A G downstream_gene_variant LIRI-JP 10 92984062 92984062 single base substitution A G intron_variant LIRI-JP 10 92984178 92984178 single base substitution A G downstream_gene_variant LIRI-JP 10 92984178 92984178 single base substitution A G intron_variant LIRI-JP 10 92984235 92984235 single base substitution T G downstream_gene_variant LIRI-JP 10 92984235 92984235 single base substitution T G intron_variant LIRI-JP 10 92985157 92985157 single base substitution G C downstream_gene_variant LIRI-JP 10 92985157 92985157 single base substitution G C intron_variant LIRI-JP 10 92985318 92985318 single base substitution G A downstream_gene_variant LIRI-JP 10 92985318 92985318 single base substitution G A intron_variant LIRI-JP 10 92987674 92987674 single base substitution T A downstream_gene_variant LIRI-JP 10 92987674 92987674 single base substitution T A exon_variant LIRI-JP 10 92987674 92987674 single base substitution T A intron_variant LIRI-JP 10 92989047 92989047 single base substitution A G downstream_gene_variant LIRI-JP 10 92989047 92989047 single base substitution A G intron_variant LIRI-JP 10 92990540 92990540 single base substitution C A downstream_gene_variant LIRI-JP 10 92990540 92990540 single base substitution C A intron_variant LIRI-JP 10 92993478 92993478 single base substitution A G intron_variant LIRI-JP 10 92996162 92996162 single base substitution C A intron_variant LIRI-JP 10 92996267 92996267 single base substitution G C intron_variant LIRI-JP 10 92997494 92997494 single base substitution C T intron_variant LIRI-JP 10 93002240 93002240 single base substitution A G intron_variant LIRI-JP 10 93003365 93003365 single base substitution A G intron_variant LIRI-JP 10 93003647 93003647 single base substitution A G intron_variant LIRI-JP 10 93004011 93004011 single base substitution C T intron_variant LIRI-JP 10 93004135 93004135 single base substitution A C intron_variant LIRI-JP 10 93006085 93006085 single base substitution A G intron_variant LIRI-JP 10 93006800 93006800 single base substitution G A intron_variant LIRI-JP 10 93013360 93013360 single base substitution G A intron_variant LIRI-JP 10 93013481 93013481 single base substitution G A intron_variant LIRI-JP 10 93015577 93015577 single base substitution A T intron_variant LIRI-JP 10 93015994 93015994 single base substitution T C intron_variant LIRI-JP 10 93017075 93017075 single base substitution A G intron_variant LIRI-JP 10 93017351 93017351 single base substitution A G intron_variant LIRI-JP 10 93021068 93021068 single base substitution C G intron_variant LIRI-JP 10 93022901 93022901 single base substitution G A intron_variant LIRI-JP 10 93025018 93025018 single base substitution G A intron_variant LIRI-JP 10 93025512 93025512 single base substitution A G intron_variant LIRI-JP 10 93026739 93026739 single base substitution G C intron_variant LIRI-JP 10 93026856 93026856 single base substitution T G intron_variant LIRI-JP 10 93028830 93028830 single base substitution C T intron_variant LIRI-JP 10 93029473 93029473 single base substitution A G intron_variant LIRI-JP 10 93032061 93032061 single base substitution G A intron_variant LIRI-JP 10 93032708 93032708 single base substitution T C intron_variant LIRI-JP 10 93036463 93036463 single base substitution A G intron_variant LIRI-JP 10 93037097 93037097 single base substitution A C intron_variant LIRI-JP 10 93039049 93039049 single base substitution G T 3_prime_UTR_variant LIRI-JP 10 93039049 93039049 single base substitution G T downstream_gene_variant LIRI-JP 10 93040357 93040357 insertion of <=200bp - A 3_prime_UTR_variant LIRI-JP 10 93040357 93040357 insertion of <=200bp - A downstream_gene_variant LIRI-JP 10 93043103 93043103 single base substitution T C 3_prime_UTR_variant LIRI-JP 10 93043103 93043103 single base substitution T C downstream_gene_variant LIRI-JP 10 93043902 93043902 single base substitution A C 3_prime_UTR_variant LIRI-JP 10 93044504 93044506 deletion of <=200bp GTT - downstream_gene_variant LIRI-JP 10 93044732 93044732 single base substitution C A downstream_gene_variant LIRI-JP 10 93044808 93044808 single base substitution A G downstream_gene_variant LIRI-JP 10 93044843 93044843 single base substitution A G downstream_gene_variant LIRI-JP 10 93045836 93045836 single base substitution A G downstream_gene_variant LIRI-JP 10 93049048 93049048 single base substitution T C downstream_gene_variant LUSC-KR 10 92979369 92979369 single base substitution A G upstream_gene_variant LUSC-KR 10 92980876 92980876 single base substitution G T intron_variant LUSC-KR 10 92982025 92982025 single base substitution C T intron_variant LUSC-KR 10 92998706 92998706 single base substitution G T intron_variant LUSC-KR 10 93016658 93016658 single base substitution A G intron_variant LUSC-KR 10 93021168 93021168 single base substitution C T missense_variant P187L 560C>T LUSC-KR 10 93047877 93047877 single base substitution C T downstream_gene_variant LUSC-US 10 93008287 93008287 single base substitution A G missense_variant I79V 235A>G MALY-DE 10 92990915 92990915 single base substitution A G downstream_gene_variant MALY-DE 10 92990915 92990915 single base substitution A G intron_variant MALY-DE 10 93009075 93009075 single base substitution T A intron_variant MALY-DE 10 93046902 93046902 single base substitution G C downstream_gene_variant MELA-AU 10 92975041 92975041 single base substitution C T upstream_gene_variant MELA-AU 10 92975612 92975612 single base substitution C T upstream_gene_variant MELA-AU 10 92975787 92975787 single base substitution C T upstream_gene_variant MELA-AU 10 92976137 92976137 single base substitution C T upstream_gene_variant MELA-AU 10 92977460 92977460 single base substitution C T upstream_gene_variant MELA-AU 10 92978318 92978318 single base substitution C T upstream_gene_variant MELA-AU 10 92978760 92978760 single base substitution T A upstream_gene_variant MELA-AU 10 92979004 92979005 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 10 92979014 92979014 single base substitution C T upstream_gene_variant MELA-AU 10 92979025 92979025 single base substitution G A upstream_gene_variant MELA-AU 10 92980121 92980121 single base substitution C T intron_variant MELA-AU 10 92980121 92980121 single base substitution C T splice_region_variant MELA-AU 10 92980121 92980121 single base substitution C T upstream_gene_variant MELA-AU 10 92981380 92981380 single base substitution T C intron_variant MELA-AU 10 92981480 92981480 single base substitution T A intron_variant MELA-AU 10 92982649 92982649 single base substitution C T exon_variant MELA-AU 10 92982649 92982649 single base substitution C T synonymous_variant H7H 21C>T MELA-AU 10 92983190 92983190 single base substitution C T downstream_gene_variant MELA-AU 10 92983190 92983190 single base substitution C T intron_variant MELA-AU 10 92983336 92983336 single base substitution T G downstream_gene_variant MELA-AU 10 92983336 92983336 single base substitution T G intron_variant MELA-AU 10 92985151 92985151 single base substitution C T downstream_gene_variant MELA-AU 10 92985151 92985151 single base substitution C T intron_variant MELA-AU 10 92985754 92985754 single base substitution G A downstream_gene_variant MELA-AU 10 92985754 92985754 single base substitution G A intron_variant MELA-AU 10 92985899 92985899 single base substitution C T downstream_gene_variant MELA-AU 10 92985899 92985899 single base substitution C T intron_variant MELA-AU 10 92986545 92986545 single base substitution C T downstream_gene_variant MELA-AU 10 92986545 92986545 single base substitution C T intron_variant MELA-AU 10 92987444 92987444 single base substitution C T downstream_gene_variant MELA-AU 10 92987444 92987444 single base substitution C T exon_variant MELA-AU 10 92987444 92987444 single base substitution C T intron_variant MELA-AU 10 92987455 92987455 single base substitution C T downstream_gene_variant MELA-AU 10 92987455 92987455 single base substitution C T exon_variant MELA-AU 10 92987455 92987455 single base substitution C T intron_variant MELA-AU 10 92987735 92987735 single base substitution C T downstream_gene_variant MELA-AU 10 92987735 92987735 single base substitution C T intron_variant MELA-AU 10 92988135 92988135 single base substitution C T downstream_gene_variant MELA-AU 10 92988135 92988135 single base substitution C T intron_variant MELA-AU 10 92988502 92988502 single base substitution C T downstream_gene_variant MELA-AU 10 92988502 92988502 single base substitution C T intron_variant MELA-AU 10 92988889 92988889 single base substitution A T downstream_gene_variant MELA-AU 10 92988889 92988889 single base substitution A T intron_variant MELA-AU 10 92989327 92989327 single base substitution C T downstream_gene_variant MELA-AU 10 92989327 92989327 single base substitution C T intron_variant MELA-AU 10 92990765 92990765 single base substitution C T downstream_gene_variant MELA-AU 10 92990765 92990765 single base substitution C T intron_variant MELA-AU 10 92992291 92992291 single base substitution C T downstream_gene_variant MELA-AU 10 92992291 92992291 single base substitution C T intron_variant MELA-AU 10 92993812 92993812 single base substitution C T intron_variant MELA-AU 10 92994033 92994033 single base substitution G A intron_variant MELA-AU 10 92995210 92995210 single base substitution C A intron_variant MELA-AU 10 92995829 92995829 single base substitution C T intron_variant MELA-AU 10 92996436 92996436 single base substitution G A intron_variant MELA-AU 10 92997155 92997155 single base substitution T C intron_variant MELA-AU 10 92998472 92998472 single base substitution C T intron_variant MELA-AU 10 92998632 92998632 single base substitution C T intron_variant MELA-AU 10 92999142 92999142 single base substitution C T intron_variant MELA-AU 10 92999745 92999745 single base substitution C T intron_variant MELA-AU 10 92999916 92999916 single base substitution T A intron_variant MELA-AU 10 93001001 93001001 deletion of <=200bp T - intron_variant MELA-AU 10 93001024 93001024 single base substitution C T intron_variant MELA-AU 10 93002236 93002236 single base substitution C T intron_variant MELA-AU 10 93002989 93002989 single base substitution C T intron_variant MELA-AU 10 93003043 93003043 single base substitution A T intron_variant MELA-AU 10 93003145 93003145 single base substitution A G intron_variant MELA-AU 10 93003177 93003177 single base substitution A C intron_variant MELA-AU 10 93003532 93003532 single base substitution T C intron_variant MELA-AU 10 93007434 93007434 single base substitution A T intron_variant MELA-AU 10 93008767 93008767 single base substitution C T intron_variant MELA-AU 10 93010885 93010885 single base substitution C T intron_variant MELA-AU 10 93012810 93012810 single base substitution C T intron_variant MELA-AU 10 93013189 93013189 single base substitution G T intron_variant MELA-AU 10 93013833 93013833 single base substitution C T intron_variant MELA-AU 10 93014149 93014149 single base substitution T C intron_variant MELA-AU 10 93014324 93014324 single base substitution C T intron_variant MELA-AU 10 93014918 93014918 single base substitution G A intron_variant MELA-AU 10 93015411 93015411 single base substitution G A intron_variant MELA-AU 10 93015431 93015431 single base substitution G A intron_variant MELA-AU 10 93016270 93016270 single base substitution G A intron_variant MELA-AU 10 93017007 93017007 single base substitution A G intron_variant MELA-AU 10 93017212 93017212 single base substitution C T intron_variant MELA-AU 10 93020404 93020404 single base substitution C T intron_variant MELA-AU 10 93020432 93020432 single base substitution C T intron_variant MELA-AU 10 93020717 93020717 single base substitution A G intron_variant MELA-AU 10 93022192 93022192 single base substitution G A intron_variant MELA-AU 10 93022413 93022414 multiple base substitution (>=2bp and <=200bp) TC GT intron_variant MELA-AU 10 93022814 93022814 single base substitution C T intron_variant MELA-AU 10 93024624 93024624 single base substitution C T intron_variant MELA-AU 10 93025040 93025040 single base substitution T C intron_variant MELA-AU 10 93027519 93027519 single base substitution C T intron_variant MELA-AU 10 93029332 93029332 single base substitution C T intron_variant MELA-AU 10 93029599 93029599 single base substitution C T intron_variant MELA-AU 10 93029835 93029835 single base substitution A T intron_variant MELA-AU 10 93033834 93033834 single base substitution C T intron_variant MELA-AU 10 93034659 93034659 single base substitution G A intron_variant MELA-AU 10 93037075 93037075 single base substitution T A intron_variant MELA-AU 10 93037077 93037077 single base substitution C T intron_variant MELA-AU 10 93038909 93038909 single base substitution T A 3_prime_UTR_variant MELA-AU 10 93038909 93038909 single base substitution T A downstream_gene_variant MELA-AU 10 93041798 93041798 single base substitution T A 3_prime_UTR_variant MELA-AU 10 93041798 93041798 single base substitution T A downstream_gene_variant MELA-AU 10 93043015 93043015 single base substitution C T 3_prime_UTR_variant MELA-AU 10 93043015 93043015 single base substitution C T downstream_gene_variant MELA-AU 10 93043035 93043035 single base substitution T A 3_prime_UTR_variant MELA-AU 10 93043035 93043035 single base substitution T A downstream_gene_variant MELA-AU 10 93045895 93045895 single base substitution C T downstream_gene_variant MELA-AU 10 93047409 93047410 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 10 93047464 93047464 single base substitution G A downstream_gene_variant MELA-AU 10 93047577 93047577 single base substitution C A downstream_gene_variant MELA-AU 10 93047814 93047814 single base substitution C T downstream_gene_variant MELA-AU 10 93047988 93047988 single base substitution C T downstream_gene_variant ORCA-IN 10 92996690 92996690 single base substitution G C intron_variant ORCA-IN 10 93015831 93015831 single base substitution G A intron_variant ORCA-IN 10 93024217 93024217 single base substitution G A missense_variant M201I 603G>A ORCA-IN 10 93037800 93037800 single base substitution G A intron_variant ORCA-IN 10 93045263 93045263 single base substitution G A downstream_gene_variant OV-AU 10 92976852 92976852 single base substitution A G upstream_gene_variant OV-AU 10 92977202 92977202 single base substitution A T upstream_gene_variant OV-AU 10 92982418 92982418 single base substitution C T intron_variant OV-AU 10 92990805 92990805 single base substitution G C downstream_gene_variant OV-AU 10 92990805 92990805 single base substitution G C intron_variant OV-AU 10 92993340 92993340 single base substitution C A intron_variant OV-AU 10 92999248 92999248 single base substitution G C intron_variant OV-AU 10 93001411 93001411 single base substitution T C intron_variant OV-AU 10 93002834 93002834 single base substitution A G intron_variant OV-AU 10 93004737 93004737 single base substitution A G intron_variant OV-AU 10 93008108 93008108 single base substitution A T intron_variant OV-AU 10 93008741 93008741 single base substitution T G intron_variant OV-AU 10 93011669 93011669 single base substitution G A intron_variant OV-AU 10 93013956 93013956 single base substitution A C intron_variant OV-AU 10 93027746 93027746 single base substitution A C intron_variant PACA-AU 10 92979896 92979896 single base substitution A C upstream_gene_variant PACA-AU 10 92984276 92984276 single base substitution T A downstream_gene_variant PACA-AU 10 92984276 92984276 single base substitution T A intron_variant PACA-AU 10 92985704 92985704 single base substitution G C downstream_gene_variant PACA-AU 10 92985704 92985704 single base substitution G C intron_variant PACA-AU 10 92987889 92987889 deletion of <=200bp T - downstream_gene_variant PACA-AU 10 92987889 92987889 deletion of <=200bp T - intron_variant PACA-AU 10 92996874 92996874 deletion of <=200bp T - intron_variant PACA-AU 10 92998941 92998941 single base substitution G T intron_variant PACA-AU 10 93006684 93006684 single base substitution T A intron_variant PACA-AU 10 93006816 93006816 single base substitution A G intron_variant PACA-AU 10 93017567 93017567 single base substitution C T intron_variant PACA-AU 10 93021332 93021332 single base substitution T C intron_variant PACA-AU 10 93021765 93021765 single base substitution T A intron_variant PACA-AU 10 93024260 93024260 single base substitution C T stop_gained R216* 646C>T PACA-AU 10 93029412 93029412 single base substitution G C intron_variant PACA-AU 10 93029688 93029688 single base substitution G A intron_variant PACA-AU 10 93041160 93041160 single base substitution A T 3_prime_UTR_variant PACA-AU 10 93041160 93041160 single base substitution A T downstream_gene_variant PACA-AU 10 93045576 93045576 single base substitution C A downstream_gene_variant PACA-CA 10 92979406 92979406 single base substitution G T upstream_gene_variant PACA-CA 10 92983545 92983545 single base substitution A T downstream_gene_variant PACA-CA 10 92983545 92983545 single base substitution A T intron_variant PACA-CA 10 92985102 92985102 single base substitution C T downstream_gene_variant PACA-CA 10 92985102 92985102 single base substitution C T intron_variant PACA-CA 10 92990402 92990402 single base substitution G A downstream_gene_variant PACA-CA 10 92990402 92990402 single base substitution G A intron_variant PACA-CA 10 92992391 92992391 single base substitution A G downstream_gene_variant PACA-CA 10 92992391 92992391 single base substitution A G intron_variant PACA-CA 10 92993336 92993336 single base substitution A C intron_variant PACA-CA 10 92996671 92996671 single base substitution A C intron_variant PACA-CA 10 92997077 92997077 single base substitution C T intron_variant PACA-CA 10 92997329 92997329 single base substitution G A intron_variant PACA-CA 10 92998703 92998703 single base substitution G A intron_variant PACA-CA 10 92999340 92999340 single base substitution G T intron_variant PACA-CA 10 93001214 93001214 single base substitution G A intron_variant PACA-CA 10 93002105 93002105 single base substitution T G intron_variant PACA-CA 10 93002881 93002881 single base substitution A C intron_variant PACA-CA 10 93005088 93005088 single base substitution T A intron_variant PACA-CA 10 93005150 93005150 single base substitution A G intron_variant PACA-CA 10 93005188 93005188 single base substitution T G intron_variant PACA-CA 10 93023638 93023638 single base substitution G C intron_variant PACA-CA 10 93025931 93025931 single base substitution A C intron_variant PACA-CA 10 93026794 93026796 deletion of <=200bp TCA - intron_variant PACA-CA 10 93026798 93026798 deletion of <=200bp A - intron_variant PACA-CA 10 93031062 93031062 single base substitution G A intron_variant PACA-CA 10 93031315 93031315 insertion of <=200bp - AA intron_variant PACA-CA 10 93033441 93033441 deletion of <=200bp C - intron_variant PACA-CA 10 93033796 93033796 single base substitution A G intron_variant PACA-CA 10 93035253 93035253 single base substitution A G intron_variant PACA-CA 10 93039943 93039943 single base substitution T G 3_prime_UTR_variant PACA-CA 10 93039943 93039943 single base substitution T G downstream_gene_variant PACA-CA 10 93045297 93045297 single base substitution A C downstream_gene_variant PAEN-IT 10 93013082 93013082 single base substitution C A intron_variant PBCA-DE 10 92987744 92987744 single base substitution G T downstream_gene_variant PBCA-DE 10 92987744 92987744 single base substitution G T intron_variant PBCA-DE 10 92998887 92998887 single base substitution C T intron_variant PBCA-DE 10 93000800 93000801 deletion of <=200bp AT - intron_variant PBCA-DE 10 93005476 93005476 single base substitution C T intron_variant PBCA-DE 10 93010789 93010789 single base substitution C A intron_variant PBCA-DE 10 93013961 93013962 deletion of <=200bp GT - intron_variant PBCA-DE 10 93025370 93025370 single base substitution A T intron_variant PBCA-DE 10 93027400 93027400 single base substitution A G intron_variant PBCA-DE 10 93030653 93030653 single base substitution T A intron_variant PRAD-CA 10 92975033 92975033 single base substitution T C upstream_gene_variant PRAD-CA 10 92978745 92978745 single base substitution A G upstream_gene_variant PRAD-CA 10 92979462 92979462 single base substitution G C upstream_gene_variant PRAD-CA 10 92982600 92982600 single base substitution C T 5_prime_UTR_variant PRAD-CA 10 92982600 92982600 single base substitution C T exon_variant PRAD-CA 10 92989473 92989473 single base substitution T C downstream_gene_variant PRAD-CA 10 92989473 92989473 single base substitution T C intron_variant PRAD-CA 10 92990402 92990402 single base substitution G A downstream_gene_variant PRAD-CA 10 92990402 92990402 single base substitution G A intron_variant PRAD-CA 10 92993994 92993994 single base substitution A C intron_variant PRAD-CA 10 93006428 93006428 single base substitution T C intron_variant PRAD-CA 10 93006730 93006730 single base substitution A G intron_variant PRAD-CA 10 93018994 93018994 single base substitution C G intron_variant PRAD-UK 10 92975210 92975210 single base substitution G A upstream_gene_variant PRAD-UK 10 92977537 92977537 single base substitution A T upstream_gene_variant PRAD-UK 10 92990328 92990328 single base substitution C T downstream_gene_variant PRAD-UK 10 92990328 92990328 single base substitution C T intron_variant PRAD-UK 10 93001523 93001523 single base substitution C G intron_variant PRAD-UK 10 93007259 93007259 single base substitution G T intron_variant PRAD-UK 10 93015196 93015196 single base substitution A G intron_variant PRAD-UK 10 93026022 93026022 single base substitution T A intron_variant PRAD-UK 10 93038521 93038521 single base substitution T C 3_prime_UTR_variant PRAD-UK 10 93038521 93038521 single base substitution T C downstream_gene_variant PRAD-UK 10 93043496 93043496 single base substitution A T 3_prime_UTR_variant RECA-EU 10 92977824 92977824 single base substitution G A upstream_gene_variant RECA-EU 10 92991067 92991067 single base substitution G A downstream_gene_variant RECA-EU 10 92991067 92991067 single base substitution G A intron_variant RECA-EU 10 92997238 92997238 single base substitution G A intron_variant RECA-EU 10 92998952 92998952 single base substitution T G intron_variant RECA-EU 10 93003810 93003810 single base substitution A T intron_variant RECA-EU 10 93028996 93028996 single base substitution G T intron_variant RECA-EU 10 93030823 93030823 single base substitution T G intron_variant RECA-EU 10 93037696 93037696 single base substitution A C intron_variant RECA-EU 10 93038680 93038680 single base substitution A T 3_prime_UTR_variant RECA-EU 10 93038680 93038680 single base substitution A T downstream_gene_variant RECA-EU 10 93045775 93045775 single base substitution A G downstream_gene_variant SKCA-BR 10 92982238 92982238 single base substitution G A intron_variant SKCA-BR 10 92998327 92998327 single base substitution C T intron_variant SKCA-BR 10 93000105 93000105 single base substitution G A intron_variant SKCA-BR 10 93006722 93006734 deletion of <=200bp GGATAGATAGATA - intron_variant SKCA-BR 10 93006734 93006734 single base substitution A G intron_variant SKCA-BR 10 93007783 93007783 single base substitution T C intron_variant SKCA-BR 10 93015401 93015401 single base substitution C T intron_variant SKCA-BR 10 93015561 93015561 single base substitution C A intron_variant SKCA-BR 10 93015561 93015561 single base substitution C T intron_variant SKCA-BR 10 93017004 93017004 single base substitution C T intron_variant SKCA-BR 10 93032373 93032373 single base substitution T A intron_variant SKCA-BR 10 93032443 93032443 single base substitution T G intron_variant SKCA-BR 10 93032638 93032638 single base substitution A C intron_variant SKCA-BR 10 93034428 93034428 single base substitution A G intron_variant SKCA-BR 10 93035364 93035364 insertion of <=200bp - AT intron_variant SKCA-BR 10 93035400 93035400 single base substitution C G intron_variant SKCM-US 10 92982654 92982654 single base substitution T G exon_variant SKCM-US 10 92982654 92982654 single base substitution T G missense_variant V9G 26T>G SKCM-US 10 93000322 93000322 single base substitution C T missense_variant P65L 194C>T SKCM-US 10 93038033 93038033 single base substitution C T missense_variant P244L 731C>T STAD-US 10 92982626 92982626 single base substitution C T 5_prime_UTR_premature_start_codon_gain_variant STAD-US 10 92982626 92982626 single base substitution C T exon_variant STAD-US 10 93011167 93011167 single base substitution T A missense_variant N148K 444T>A STAD-US 10 93021088 93021088 deletion of <=200bp A - frameshift_variant L160 STAD-US 10 93024260 93024260 single base substitution C T stop_gained R216* 646C>T STAD-US 10 93038067 93038067 single base substitution C T synonymous_variant F255F 765C>T THCA-SA 10 93043858 93043858 single base substitution T C 3_prime_UTR_variant UCEC-US 10 92982636 92982636 single base substitution C T exon_variant UCEC-US 10 92982636 92982636 single base substitution C T missense_variant T3I 8C>T UCEC-US 10 92982723 92982723 single base substitution C T downstream_gene_variant UCEC-US 10 92982723 92982723 single base substitution C T exon_variant UCEC-US 10 92982723 92982723 single base substitution C T missense_variant T32M 95C>T UCEC-US 10 93000278 93000278 single base substitution C T synonymous_variant S50S 150C>T UCEC-US 10 93008299 93008299 single base substitution G A missense_variant V83I 247G>A UCEC-US 10 93008435 93008435 single base substitution T C synonymous_variant R93R 279T>C UCEC-US 10 93021104 93021104 single base substitution C T stop_gained R166* 496C>T UCEC-US 10 93024196 93024196 single base substitution G A synonymous_variant V194V 582G>A UCEC-US 10 93031398 93031398 single base substitution C T missense_variant R223W 667C>T UCEC-US 10 93038067 93038067 single base substitution C A missense_variant F255L 765C>A UCEC-US 10 93038067 93038067 single base substitution C T synonymous_variant F255F 765C>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand RK021_C01 COSM1627672 c.112T>A p.F38I Substitution - Missense 10:91222983-91222983 + TCGA-B5-A11E-01 COSM921374 c.247G>A p.V83I Substitution - Missense 10:91248542-91248542 + TCGA-A5-A0GB-01 COSM921371 c.8C>T p.T3I Substitution - Missense 10:91222879-91222879 + TCGA-D7-A4YV-01 COSM921379 c.765C>T p.F255F Substitution - coding silent 10:91278310-91278310 + TCGA-D5-6928-01 COSM1349759 c.395A>G p.Y132C Substitution - Missense 10:91251361-91251361 + TCGA-CA-6717-01 COSM921379 c.765C>T p.F255F Substitution - coding silent 10:91278310-91278310 + TCGA-NH-A5IV-01 COSM1349761 c.668G>A p.R223Q Substitution - Missense 10:91271642-91271642 + I2L-P10-Tumor-Organoid COSM5359856 c.627C>A p.F209L Substitution - Missense 10:91264484-91264484 + TCGA-BS-A0UL-01 COSM921373 c.150C>T p.S50S Substitution - coding silent 10:91240521-91240521 + TCGA-34-5231-01 COSM686102 c.235A>G p.I79V Substitution - Missense 10:91248530-91248530 + TCGA-A6-5661-01 COSM1349758 c.326-2A>G p.? Unknown 10:91251290-91251290 + TCGA-AP-A059-01 COSM921377 c.582G>A p.V194V Substitution - coding silent 10:91264439-91264439 + TCGA-GN-A26C-01 COSM3441477 c.731C>T p.P244L Substitution - Missense 10:91278276-91278276 + TCGA-D5-6539-01 COSM1969262 c.664-4G>A p.? Unknown 10:91271634-91271634 + TCGA-AX-A05Z-01 COSM921379 c.765C>T p.F255F Substitution - coding silent 10:91278310-91278310 + 90273 COSM330227 c.275A>G p.E92G Substitution - Missense 10:91248674-91248674 + J88_T COSM3978896 c.560C>T p.P187L Substitution - Missense 10:91261411-91261411 + ESO-0459 COSM1261518 c.259C>T p.R87* Substitution - Nonsense 10:91248554-91248554 + TCGA-14-2554-01 COSM921379 c.765C>T p.F255F Substitution - coding silent 10:91278310-91278310 + TCGA-AP-A0LT-01 COSM921375 c.279T>C p.R93R Substitution - coding silent 10:91248678-91248678 + DLD1 COSM4621907 c.135G>A p.Q45Q Substitution - coding silent 10:91240506-91240506 + TCGA-AZ-6601-01 COSM5142159 c.663+1G>A p.? Unknown 10:91264521-91264521 + TCGA-BG-A0VZ-01 COSM921372 c.95C>T p.T32M Substitution - Missense 10:91222966-91222966 + TCGA-B5-A11E-01 COSM921378 c.667C>T p.R223W Substitution - Missense 10:91271641-91271641 + TCGA-JW-A5VG-01 COSM4818366 c.457G>A p.G153R Substitution - Missense 10:91251423-91251423 + TCGA-FU-A3HZ-01 COSM4839321 c.531A>C p.K177N Substitution - Missense 10:91261382-91261382 + TCGA-BR-4184-01 COSM3383080 c.646C>T p.R216* Substitution - Nonsense 10:91264503-91264503 + TCGA-FS-A4F5-06 COSM3441476 c.194C>T p.P65L Substitution - Missense 10:91240565-91240565 + TCGA-B5-A0JY-01 COSM921380 c.765C>A p.F255L Substitution - Missense 10:91278310-91278310 + TCGA-CG-4469-01 COSM4016571 c.444T>A p.N148K Substitution - Missense 10:91251410-91251410 + Pat_70_A COSM4712696 c.265+1G>A p.? Unknown 10:91248561-91248561 + PD7249a COSM1261518 c.259C>T p.R87* Substitution - Nonsense 10:91248554-91248554 + Patient1 COSM1166818 c.106C>A p.H36N Substitution - Missense 10:91222977-91222977 + 1N38-VS-1T38 COSM1969264 c.683C>G p.S228* Substitution - Nonsense 10:91271657-91271657 + YUMER COSM1702755 c.619A>G p.M207V Substitution - Missense 10:91264476-91264476 + TCGA-AA-3672-01 COSM267137 c.437T>C p.L146S Substitution - Missense 10:91251403-91251403 + TCGA-CA-6717-01 COSM1349760 c.536T>G p.F179C Substitution - Missense 10:91261387-91261387 + TCGA-AG-A002-01 COSM262829 c.529delA p.K178fs*3 Deletion - Frameshift 10:91261380-91261380 + OSCC-GB_01060111 COSM4882567 c.603G>A p.M201I Substitution - Missense 10:91264460-91264460 + TCGA-BS-A0TC-01 COSM921376 c.496C>T p.R166* Substitution - Nonsense 10:91261347-91261347 + TCGA-EE-A29D-06 COSM3868043 c.26T>G p.V9G Substitution - Missense 10:91222897-91222897 + TCGA-AP-A056-01 COSM921376 c.496C>T p.R166* Substitution - Nonsense 10:91261347-91261347 + TCGA-CA-6717-01 COSM1349761 c.668G>A p.R223Q Substitution - Missense 10:91271642-91271642 + T1743 COSM4712696 c.265+1G>A p.? Unknown 10:91248561-91248561 + NCI-H1770 COSM23469 c.669G>A p.R223R Substitution - coding silent 10:91271643-91271643 + BD121T COSM5515364 c.492C>A p.F164L Substitution - Missense 10:91261343-91261343 + 49M COSM5592426 c.133C>T p.Q45* Substitution - Nonsense 10:91240504-91240504 + CSCC-27-T COSM921378 c.667C>T p.R223W Substitution - Missense 10:91271641-91271641 + TCGA-E2-A15R-01 COSM428124 c.509G>A p.R170H Substitution - Missense 10:91261360-91261360 + KM12 COSM1969254 c.367G>C p.G123R Substitution - Missense 10:91251333-91251333 + sysucc-880T COSM3383080 c.646C>T p.R216* Substitution - Nonsense 10:91264503-91264503 + S00836 COSM314009 c.658G>T p.E220* Substitution - Nonsense 10:91264515-91264515 + Pat_32_A COSM5837444 c.209+1G>A p.? Unknown 10:91240581-91240581 + TCGA-AC-A23H-01 COSM3807970 c.379G>A p.E127K Substitution - Missense 10:91251345-91251345 + 8031867 COSM3383080 c.646C>T p.R216* Substitution - Nonsense 10:91264503-91264503 + TCGA-A8-A0A6-01 COSM3807969 c.369T>G p.G123G Substitution - coding silent 10:91251335-91251335 + CSCC-44-T COSM4489653 c.350C>T p.P117L Substitution - Missense 10:91251316-91251316 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.500498;Hs.500512 10q23.32

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C 3-UTRSNV . c.768+5832A>C 10 93043902 HC A G Missense p.I79V c.235A>G 10 93008287 LUSC C A Missense p.Q241K c.721C>A 10 93031452 GBM C G Missense p.R147G c.439C>G 10 93011162 HNSC C T 5-UTRSNV . c.1-3C>T 10 92982626 STAD C T Missense p.P244L c.731C>T 10 93038033 CM C T Missense p.T32M c.95C>T 10 92982723 UCEC C T Missense p.T3I c.8C>T 10 92982636 UCEC C T Nonsense p.R166* c.496C>T 10 93021104 UCEC C T Nonsense p.R87* c.259C>T 10 93008311 ESCA C T Synonymous p.F255F c.765C>T 10 93038067 GBM C T Synonymous p.S50S c.150C>T 10 93000278 UCEC G A Missense p.C145Y c.434G>A 10 93011157 LUAD G A Missense p.E77K c.229G>A 10 93008281 CM G A Missense p.R170H c.509G>A 10 93021117 BRCA G T Missense p.V44F c.130G>T 10 93000258 LUAD G T Nonsense p.E220* c.658G>T 10 93024272 SCLC TA - Frameshift p.I141Lfs*8 c.421_422delAT 10 93011143 RCCC T A Missense p.F38I c.112T>A 10 92982740 HC T A Missense p.N148K c.444T>A 10 93011167 STAD T C Synonymous p.R93R c.279T>C 10 93008435 UCEC T G IntronicSNV . c.574-1128T>G 10 93023060 CLL T G Nonsense p.Y249* c.747T>G 10 93038049 HNSC