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 23 153713943 153713943 + Missense_Mutation SNP G G A TCGA-C4-A0F6-01A-11D-A10S-08 TCGA-C4-A0F6-10A-01D-A10S-08 g.chrX:153713943G>A c.409C>T c.(409-411)Cgg>Tgg p.R137W BLCA 23 153713947 153713947 + Missense_Mutation SNP G G C TCGA-FD-A6TG-01A-11D-A32B-08 TCGA-FD-A6TG-10A-01D-A329-08 g.chrX:153713947G>C c.405C>G c.(403-405)atC>atG p.I135M BLCA 23 153714142 153714142 + Missense_Mutation SNP C C A TCGA-XF-AAMZ-01A-11D-A42E-08 TCGA-XF-AAMZ-10A-01D-A42H-08 g.chrX:153714142C>A c.331G>T c.(331-333)Gat>Tat p.D111Y BLCA 23 153714159 153714159 + Missense_Mutation SNP C C T TCGA-DK-AA6Q-01A-11D-A391-08 TCGA-DK-AA6Q-10A-01D-A394-08 g.chrX:153714159C>T c.314G>A c.(313-315)cGc>cAc p.R105H BLCA 23 153714208 153714208 + Missense_Mutation SNP C C T TCGA-G2-AA3D-01A-11D-A391-08 TCGA-G2-AA3D-10A-01D-A394-08 g.chrX:153714208C>T c.265G>A c.(265-267)Gac>Aac p.D89N BLCA 23 153714226 153714226 + Missense_Mutation SNP C C T TCGA-4Z-AA7M-01A-11D-A391-08 TCGA-4Z-AA7M-10A-01D-A394-08 g.chrX:153714226C>T c.247G>A c.(247-249)Gag>Aag p.E83K BLCA 23 153714279 153714279 + Missense_Mutation SNP G G C TCGA-FD-A6TG-01A-11D-A32B-08 TCGA-FD-A6TG-10A-01D-A329-08 g.chrX:153714279G>C c.194C>G c.(193-195)tCc>tGc p.S65C ESCA 23 153714147 153714147 + Missense_Mutation SNP G G A TCGA-S8-A6BV-01A-21D-A31U-09 TCGA-S8-A6BV-10A-01D-A31U-09 g.chrX:153714147G>A c.326C>T c.(325-327)gCg>gTg p.A109V GBMLGG 23 153714147 153714147 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:153714147G>A c.326C>T c.(325-327)gCg>gTg p.A109V HNSC 23 153713958 153713958 + Silent SNP G G A TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chrX:153713958G>A c.394C>T c.(394-396)Ctg>Ttg p.L132L HNSC 23 153714159 153714160 + Frame_Shift_Ins INS - - G TCGA-CQ-7071-01A-12D-A30E-08 TCGA-CQ-7071-10A-01D-A30H-08 g.chrX:153714159_153714160insG c.313_314insC c.(313-315)cgcfs p.R105fs KIPAN 23 153713966 153713966 + Missense_Mutation SNP C C T TCGA-B9-A8YI-01A-21D-A36X-10 TCGA-B9-A8YI-10A-01D-A370-10 g.chrX:153713966C>T c.386G>A c.(385-387)cGc>cAc p.R129H KIPAN 23 153714611 153714611 + Frame_Shift_Del DEL G G - TCGA-B2-5633-01A-01D-1534-10 TCGA-B2-5633-10A-01D-1535-10 g.chrX:153714611delG c.110delC c.(109-111)ccafs p.P37fs KIRC 23 153714611 153714611 + Frame_Shift_Del DEL G G - TCGA-B2-5633-01A-01D-1534-10 TCGA-B2-5633-10A-01D-1535-10 g.chrX:153714611delG c.110delC c.(109-111)ccafs p.P37fs KIRP 23 153713966 153713966 + Missense_Mutation SNP C C T TCGA-B9-A8YI-01A-21D-A36X-10 TCGA-B9-A8YI-10A-01D-A370-10 g.chrX:153713966C>T c.386G>A c.(385-387)cGc>cAc p.R129H LGG 23 153714147 153714147 + Missense_Mutation SNP G G A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chrX:153714147G>A c.326C>T c.(325-327)gCg>gTg p.A109V LIHC 23 153714302 153714302 + Silent SNP C C T TCGA-DD-AADY-01A-11D-A40R-10 TCGA-DD-AADY-10A-01D-A40U-10 g.chrX:153714302C>T c.171G>A c.(169-171)tcG>tcA p.S57S LUSC 23 153713988 153713988 + Splice_Site SNP C C A TCGA-60-2698-01A-01D-1522-08 TCGA-60-2698-11A-01D-1522-08 g.chrX:153713988C>A c.364G>T c.(364-366)Gat>Tat p.D122Y PCPG 23 153714628 153714628 + Frame_Shift_Del DEL G G - TCGA-WB-A81I-01A-11D-A35I-08 TCGA-WB-A81I-10A-01D-A35G-08 g.chrX:153714628delG c.93delC c.(91-93)tccfs p.S31fs

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation ALL-US X 153714310 153714310 single base substitution G A downstream_gene_variant ALL-US X 153714310 153714310 single base substitution G A exon_variant ALL-US X 153714310 153714310 single base substitution G A stop_gained R55* 163C>T BLCA-US X 153713943 153713943 single base substitution G A 3_prime_UTR_variant BLCA-US X 153713943 153713943 single base substitution G A downstream_gene_variant BLCA-US X 153713943 153713943 single base substitution G A exon_variant BLCA-US X 153713943 153713943 single base substitution G A missense_variant R137C 409C>T BLCA-US X 153713943 153713943 single base substitution G A missense_variant R137W 409C>T BRCA-EU X 153707163 153707163 single base substitution G C downstream_gene_variant BRCA-EU X 153707255 153707255 single base substitution G A downstream_gene_variant BRCA-EU X 153707480 153707480 single base substitution G C downstream_gene_variant BRCA-EU X 153708118 153708118 single base substitution C A downstream_gene_variant BRCA-EU X 153708421 153708421 single base substitution G T downstream_gene_variant BRCA-EU X 153708828 153708828 deletion of <=200bp C - downstream_gene_variant BRCA-EU X 153709909 153709909 single base substitution T A downstream_gene_variant BRCA-EU X 153710469 153710469 single base substitution G A downstream_gene_variant BRCA-EU X 153710808 153710808 single base substitution C T downstream_gene_variant BRCA-EU X 153711053 153711053 single base substitution A G downstream_gene_variant BRCA-EU X 153711397 153711397 single base substitution A T downstream_gene_variant BRCA-EU X 153711577 153711577 single base substitution G A downstream_gene_variant BRCA-EU X 153712626 153712626 single base substitution T C 3_prime_UTR_variant BRCA-EU X 153712626 153712626 single base substitution T C downstream_gene_variant BRCA-EU X 153712999 153712999 single base substitution G A 3_prime_UTR_variant BRCA-EU X 153712999 153712999 single base substitution G A downstream_gene_variant BRCA-EU X 153714933 153714933 single base substitution G C 5_prime_UTR_variant BRCA-EU X 153714933 153714933 single base substitution G C upstream_gene_variant BRCA-EU X 153715034 153715042 deletion of <=200bp GAGGGGCGC - upstream_gene_variant BRCA-EU X 153715129 153715129 single base substitution G C upstream_gene_variant BRCA-EU X 153717246 153717246 single base substitution G T upstream_gene_variant BRCA-EU X 153717317 153717317 single base substitution C T upstream_gene_variant BRCA-EU X 153717369 153717369 single base substitution G A upstream_gene_variant BRCA-EU X 153717778 153717778 deletion of <=200bp G - upstream_gene_variant BRCA-EU X 153717947 153717947 single base substitution C T upstream_gene_variant BRCA-EU X 153718064 153718064 single base substitution C T upstream_gene_variant BRCA-EU X 153719933 153719933 single base substitution G T upstream_gene_variant BRCA-FR X 153707163 153707163 single base substitution G C downstream_gene_variant BRCA-FR X 153707347 153707347 single base substitution G A downstream_gene_variant BRCA-FR X 153708118 153708118 single base substitution C A downstream_gene_variant BRCA-US X 153713698 153713698 single base substitution C A 3_prime_UTR_variant BRCA-US X 153713698 153713698 single base substitution C A downstream_gene_variant BRCA-US X 153713698 153713698 single base substitution C A exon_variant BRCA-US X 153713698 153713698 single base substitution C A stop_gained E172* 514G>T BRCA-US X 153713787 153713787 single base substitution C T 3_prime_UTR_variant BRCA-US X 153713787 153713787 single base substitution C T downstream_gene_variant BRCA-US X 153713787 153713787 single base substitution C T exon_variant BRCA-US X 153713787 153713787 single base substitution C T missense_variant R142H 425G>A BRCA-US X 153716008 153716008 single base substitution C A upstream_gene_variant BRCA-US X 153716037 153716037 single base substitution G A upstream_gene_variant BRCA-US X 153716489 153716489 deletion of <=200bp G - upstream_gene_variant BRCA-US X 153716700 153716700 deletion of <=200bp A - upstream_gene_variant BRCA-US X 153716703 153716703 single base substitution G T upstream_gene_variant BRCA-US X 153717203 153717203 single base substitution A G upstream_gene_variant BTCA-JP X 153713881 153713881 single base substitution T C 3_prime_UTR_variant BTCA-JP X 153713881 153713881 single base substitution T C downstream_gene_variant BTCA-JP X 153713881 153713881 single base substitution T C exon_variant BTCA-JP X 153713881 153713881 single base substitution T C intron_variant BTCA-JP X 153713881 153713881 single base substitution T C synonymous_variant K157K 471A>G BTCA-JP X 153714712 153714712 single base substitution G A intron_variant BTCA-JP X 153714712 153714712 single base substitution G A upstream_gene_variant BTCA-JP X 153716599 153716599 single base substitution C T upstream_gene_variant BTCA-JP X 153717065 153717065 single base substitution G T upstream_gene_variant BTCA-JP X 153717386 153717386 single base substitution A G upstream_gene_variant CESC-US X 153713871 153713871 single base substitution G A 3_prime_UTR_variant CESC-US X 153713871 153713871 single base substitution G A downstream_gene_variant CESC-US X 153713871 153713871 single base substitution G A exon_variant CESC-US X 153713871 153713871 single base substitution G A intron_variant CESC-US X 153716084 153716084 single base substitution A G upstream_gene_variant CESC-US X 153716978 153716978 single base substitution G A upstream_gene_variant CESC-US X 153717091 153717091 single base substitution G C upstream_gene_variant COAD-US X 153716061 153716061 deletion of <=200bp G - upstream_gene_variant COAD-US X 153716184 153716184 single base substitution C T upstream_gene_variant COAD-US X 153716439 153716439 single base substitution C T upstream_gene_variant COCA-CN X 153713943 153713943 single base substitution G A 3_prime_UTR_variant COCA-CN X 153713943 153713943 single base substitution G A downstream_gene_variant COCA-CN X 153713943 153713943 single base substitution G A exon_variant COCA-CN X 153713943 153713943 single base substitution G A missense_variant R137C 409C>T COCA-CN X 153713943 153713943 single base substitution G A missense_variant R137W 409C>T COCA-CN X 153714360 153714360 single base substitution G A downstream_gene_variant COCA-CN X 153714360 153714360 single base substitution G A exon_variant COCA-CN X 153714360 153714360 single base substitution G A intron_variant ESCA-CN X 153716827 153716827 single base substitution G T upstream_gene_variant GBM-US X 153716308 153716308 single base substitution C A upstream_gene_variant KIRC-US X 153714611 153714611 deletion of <=200bp G - exon_variant KIRC-US X 153714611 153714611 deletion of <=200bp G - frameshift_variant P37 KIRC-US X 153714611 153714611 deletion of <=200bp G - intron_variant KIRC-US X 153714611 153714611 deletion of <=200bp G - upstream_gene_variant KIRC-US X 153716013 153716013 single base substitution C G upstream_gene_variant LICA-FR X 153712539 153712539 single base substitution C T 3_prime_UTR_variant LICA-FR X 153712539 153712539 single base substitution C T downstream_gene_variant LICA-FR X 153715995 153715995 single base substitution C T upstream_gene_variant LIHC-US X 153715955 153715955 single base substitution G T upstream_gene_variant LINC-JP X 153714290 153714290 single base substitution G A downstream_gene_variant LINC-JP X 153714290 153714290 single base substitution G A exon_variant LINC-JP X 153714290 153714290 single base substitution G A synonymous_variant I61I 183C>T LINC-JP X 153715989 153715989 single base substitution C A upstream_gene_variant LIRI-JP X 153709611 153709611 single base substitution A G downstream_gene_variant LIRI-JP X 153709925 153709925 single base substitution T C downstream_gene_variant LIRI-JP X 153712102 153712102 single base substitution A G 3_prime_UTR_variant LIRI-JP X 153712102 153712102 single base substitution A G downstream_gene_variant LIRI-JP X 153712354 153712354 single base substitution A G 3_prime_UTR_variant LIRI-JP X 153712354 153712354 single base substitution A G downstream_gene_variant LIRI-JP X 153715920 153715920 single base substitution G A upstream_gene_variant LIRI-JP X 153717901 153717901 single base substitution G A upstream_gene_variant LIRI-JP X 153718066 153718066 single base substitution G A upstream_gene_variant LIRI-JP X 153718286 153718286 single base substitution A G upstream_gene_variant LUSC-US X 153713988 153713988 single base substitution C A downstream_gene_variant LUSC-US X 153713988 153713988 single base substitution C A missense_variant D122Y 364G>T LUSC-US X 153713988 153713988 single base substitution C A splice_region_variant LUSC-US X 153716116 153716116 single base substitution C A upstream_gene_variant MALY-DE X 153709503 153709503 single base substitution C T downstream_gene_variant MELA-AU X 153707330 153707330 single base substitution G A downstream_gene_variant MELA-AU X 153707360 153707360 single base substitution C A downstream_gene_variant MELA-AU X 153707406 153707406 single base substitution C T downstream_gene_variant MELA-AU X 153707780 153707780 single base substitution C T downstream_gene_variant MELA-AU X 153708125 153708125 single base substitution G A downstream_gene_variant MELA-AU X 153709389 153709389 single base substitution G A downstream_gene_variant MELA-AU X 153709827 153709827 single base substitution G A downstream_gene_variant MELA-AU X 153710267 153710267 single base substitution G A downstream_gene_variant MELA-AU X 153710357 153710357 single base substitution C T downstream_gene_variant MELA-AU X 153711648 153711648 single base substitution G A downstream_gene_variant MELA-AU X 153712219 153712219 single base substitution A G 3_prime_UTR_variant MELA-AU X 153712219 153712219 single base substitution A G downstream_gene_variant MELA-AU X 153712818 153712818 single base substitution G A 3_prime_UTR_variant MELA-AU X 153712818 153712818 single base substitution G A downstream_gene_variant MELA-AU X 153713014 153713014 single base substitution G A 3_prime_UTR_variant MELA-AU X 153713014 153713014 single base substitution G A downstream_gene_variant MELA-AU X 153713111 153713111 single base substitution G A 3_prime_UTR_variant MELA-AU X 153713111 153713111 single base substitution G A downstream_gene_variant MELA-AU X 153713123 153713123 single base substitution G A 3_prime_UTR_variant MELA-AU X 153713123 153713123 single base substitution G A downstream_gene_variant MELA-AU X 153713429 153713429 single base substitution G A 3_prime_UTR_variant MELA-AU X 153713429 153713429 single base substitution G A downstream_gene_variant MELA-AU X 153713706 153713706 single base substitution C T 3_prime_UTR_variant MELA-AU X 153713706 153713706 single base substitution C T downstream_gene_variant MELA-AU X 153713706 153713706 single base substitution C T exon_variant MELA-AU X 153713706 153713706 single base substitution C T missense_variant R169K 506G>A MELA-AU X 153714007 153714007 single base substitution G A downstream_gene_variant MELA-AU X 153714007 153714007 single base substitution G A intron_variant MELA-AU X 153714428 153714428 single base substitution A C exon_variant MELA-AU X 153714428 153714428 single base substitution A C intron_variant MELA-AU X 153714428 153714428 single base substitution A C splice_region_variant MELA-AU X 153715488 153715488 single base substitution C T upstream_gene_variant MELA-AU X 153717793 153717793 single base substitution C T upstream_gene_variant MELA-AU X 153719316 153719316 single base substitution G A upstream_gene_variant OV-AU X 153707301 153707301 single base substitution A G downstream_gene_variant OV-AU X 153708577 153708577 single base substitution T C downstream_gene_variant OV-US X 153716442 153716442 single base substitution C T upstream_gene_variant PACA-AU X 153710000 153710000 single base substitution G A downstream_gene_variant PACA-AU X 153710381 153710381 single base substitution G A downstream_gene_variant PACA-AU X 153710392 153710392 single base substitution C T downstream_gene_variant PACA-AU X 153710711 153710711 single base substitution G T downstream_gene_variant PACA-AU X 153716482 153716482 single base substitution G A upstream_gene_variant PACA-CA X 153708724 153708724 single base substitution C T downstream_gene_variant PACA-CA X 153713787 153713787 single base substitution C T 3_prime_UTR_variant PACA-CA X 153713787 153713787 single base substitution C T downstream_gene_variant PACA-CA X 153713787 153713787 single base substitution C T exon_variant PACA-CA X 153713787 153713787 single base substitution C T missense_variant R142H 425G>A PACA-CA X 153714606 153714606 single base substitution G A exon_variant PACA-CA X 153714606 153714606 single base substitution G A intron_variant PACA-CA X 153714606 153714606 single base substitution G A missense_variant R39C 115C>T PACA-CA X 153714606 153714606 single base substitution G A upstream_gene_variant PACA-CA X 153716019 153716019 single base substitution C T upstream_gene_variant PRAD-US X 153716036 153716036 single base substitution C T upstream_gene_variant READ-US X 153716358 153716358 single base substitution G A upstream_gene_variant SKCA-BR X 153709642 153709642 single base substitution T A downstream_gene_variant SKCA-BR X 153717597 153717597 single base substitution G A upstream_gene_variant SKCM-US X 153715943 153715943 single base substitution G A upstream_gene_variant SKCM-US X 153716274 153716274 single base substitution C A upstream_gene_variant SKCM-US X 153716343 153716343 single base substitution G A upstream_gene_variant SKCM-US X 153716408 153716408 single base substitution G C upstream_gene_variant SKCM-US X 153716663 153716663 single base substitution G A upstream_gene_variant SKCM-US X 153716816 153716816 single base substitution G A upstream_gene_variant SKCM-US X 153716920 153716920 single base substitution C A upstream_gene_variant SKCM-US X 153717110 153717110 single base substitution G A upstream_gene_variant STAD-US X 153713953 153713953 single base substitution G A 3_prime_UTR_variant STAD-US X 153713953 153713953 single base substitution G A downstream_gene_variant STAD-US X 153713953 153713953 single base substitution G A exon_variant STAD-US X 153713953 153713953 single base substitution G A synonymous_variant D133D 399C>T STAD-US X 153714222 153714222 single base substitution G A 3_prime_UTR_variant STAD-US X 153714222 153714222 single base substitution G A downstream_gene_variant STAD-US X 153714222 153714222 single base substitution G A exon_variant STAD-US X 153714222 153714222 single base substitution G A missense_variant A84V 251C>T STAD-US X 153715994 153715994 single base substitution G T upstream_gene_variant STAD-US X 153716404 153716404 single base substitution C T upstream_gene_variant STAD-US X 153716440 153716440 single base substitution G A upstream_gene_variant STAD-US X 153716473 153716473 deletion of <=200bp C - upstream_gene_variant STAD-US X 153716482 153716482 single base substitution G A upstream_gene_variant STAD-US X 153717161 153717161 single base substitution C T upstream_gene_variant STAD-US X 153717218 153717218 single base substitution C T upstream_gene_variant THCA-SA X 153712888 153712888 single base substitution C T 3_prime_UTR_variant THCA-SA X 153712888 153712888 single base substitution C T downstream_gene_variant THCA-SA X 153713167 153713167 single base substitution G A 3_prime_UTR_variant THCA-SA X 153713167 153713167 single base substitution G A downstream_gene_variant THCA-SA X 153713451 153713451 single base substitution C T 3_prime_UTR_variant THCA-SA X 153713451 153713451 single base substitution C T downstream_gene_variant THCA-SA X 153713787 153713787 single base substitution C T 3_prime_UTR_variant THCA-SA X 153713787 153713787 single base substitution C T downstream_gene_variant THCA-SA X 153713787 153713787 single base substitution C T exon_variant THCA-SA X 153713787 153713787 single base substitution C T missense_variant R142H 425G>A UCEC-US X 153713947 153713947 single base substitution G A 3_prime_UTR_variant UCEC-US X 153713947 153713947 single base substitution G A downstream_gene_variant UCEC-US X 153713947 153713947 single base substitution G A exon_variant UCEC-US X 153713947 153713947 single base substitution G A synonymous_variant I135I 405C>T UCEC-US X 153714111 153714111 single base substitution C A downstream_gene_variant UCEC-US X 153714111 153714111 single base substitution C A missense_variant R121M 362G>T UCEC-US X 153714111 153714111 single base substitution C A splice_region_variant UCEC-US X 153714142 153714142 single base substitution C A 3_prime_UTR_variant UCEC-US X 153714142 153714142 single base substitution C A downstream_gene_variant UCEC-US X 153714142 153714142 single base substitution C A exon_variant UCEC-US X 153714142 153714142 single base substitution C A missense_variant D111Y 331G>T UCEC-US X 153714191 153714191 single base substitution C A 3_prime_UTR_variant UCEC-US X 153714191 153714191 single base substitution C A downstream_gene_variant UCEC-US X 153714191 153714191 single base substitution C A exon_variant UCEC-US X 153714191 153714191 single base substitution C A missense_variant Q94H 282G>T UCEC-US X 153714218 153714218 single base substitution C A 3_prime_UTR_variant UCEC-US X 153714218 153714218 single base substitution C A downstream_gene_variant UCEC-US X 153714218 153714218 single base substitution C A exon_variant UCEC-US X 153714218 153714218 single base substitution C A missense_variant Q85H 255G>T UCEC-US X 153714303 153714303 single base substitution G A downstream_gene_variant UCEC-US X 153714303 153714303 single base substitution G A exon_variant UCEC-US X 153714303 153714303 single base substitution G A missense_variant S57L 170C>T UCEC-US X 153716359 153716359 single base substitution G A upstream_gene_variant UCEC-US X 153716389 153716389 single base substitution G A upstream_gene_variant UCEC-US X 153716396 153716396 single base substitution G A upstream_gene_variant UCEC-US X 153716640 153716640 single base substitution C T upstream_gene_variant UCEC-US X 153716663 153716663 single base substitution G A upstream_gene_variant UCEC-US X 153716714 153716714 single base substitution T C upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand Gp2D COSM3034458 c.322A>G p.S108G Substitution - Missense 23:154485812-154485812 - Detroit_562 COSM4594665 c.95A>G p.E32G Substitution - Missense 23:154486287-154486287 - UM-SCC-4 COSM4593998 c.268T>C p.S90P Substitution - Missense 23:154485866-154485866 - TCGA-HU-A4GC-01 COSM4108161 c.399C>T p.D133D Substitution - coding silent 23:154485614-154485614 - TCGA-D1-A0ZO-01 COSM1118069 c.282G>T p.Q94H Substitution - Missense 23:154485852-154485852 - HCC64 COSM3034461 c.183C>T p.I61I Substitution - coding silent 23:154485951-154485951 - YUOTHO COSM5412336 c.213C>T p.V71V Substitution - coding silent 23:154485921-154485921 - 9105_T COSM5043417 c.392C>A p.T131K Substitution - Missense 23:154485621-154485621 - TCGA-B5-A0K9-01 COSM1118072 c.170C>T p.S57L Substitution - Missense 23:154485964-154485964 - UD-SCC-2 COSM4593998 c.268T>C p.S90P Substitution - Missense 23:154485866-154485866 - CAL33 COSM4593998 c.268T>C p.S90P Substitution - Missense 23:154485866-154485866 - PASLZM COSM5006511 c.163C>T p.R55* Substitution - Nonsense 23:154485971-154485971 - T276 COSM4738760 c.246C>T p.G82G Substitution - coding silent 23:154485888-154485888 - DLD1 COSM3034454 c.379C>A p.L127M Substitution - Missense 23:154485634-154485634 - TCGA-AP-A059-01 COSM1118071 c.255G>T p.Q85H Substitution - Missense 23:154485879-154485879 - TCGA-BR-8081-01 COSM4108162 c.251C>T p.A84V Substitution - Missense 23:154485883-154485883 - SW620 COSM3034455 c.377C>T p.S126F Substitution - Missense 23:154485636-154485636 - T3090 COSM4738758 c.338G>A p.S113N Substitution - Missense 23:154485796-154485796 - TCGA-BS-A0UF-01 COSM1118065 c.405C>T p.I135I Substitution - coding silent 23:154485608-154485608 - PCSI_0170_Pa_P_526 COSM4964963 c.115C>T p.R39C Substitution - Missense 23:154486267-154486267 - LUAD-LIP77 COSM367972 c.171G>A p.S57S Substitution - coding silent 23:154485963-154485963 - TCGA-C4-A0F6-01 COSM422176 c.409C>T p.R137W Substitution - Missense 23:154485604-154485604 - TCGA-60-2698-01 COSM756793 c.364G>T p.D122Y Substitution - Missense 23:154485649-154485649 - Detroit_562 COSM4594912 c.92C>A p.S31Y Substitution - Missense 23:154486290-154486290 - LUAD-S01346 COSM404362 c.280C>T p.Q94* Substitution - Nonsense 23:154485854-154485854 - HCC64T COSM3034461 c.183C>T p.I61I Substitution - coding silent 23:154485951-154485951 - CAL27 COSM4593998 c.268T>C p.S90P Substitution - Missense 23:154485866-154485866 - UPCI:SCC090 COSM4593998 c.268T>C p.S90P Substitution - Missense 23:154485866-154485866 - I2L-P19Ta-Tumor-Organoid COSM5367053 c.126G>A p.R42R Substitution - coding silent 23:154486256-154486256 - 40M COSM5586948 c.462C>T p.G154G Substitution - coding silent 23:154485551-154485551 - TCGA-D1-A0ZO-01 COSM1118066 c.362G>T p.R121M Substitution - Missense 23:154485772-154485772 - TCGA-B5-A0K4-01 COSM1118068 c.326C>T p.A109V Substitution - Missense 23:154485808-154485808 - sysucc-1370T COSM422176 c.409C>T p.R137W Substitution - Missense 23:154485604-154485604 - BD72T COSM5513923 c.471A>G p.K157K Substitution - coding silent 23:154485542-154485542 - TCGA-AP-A0LM-01 COSM1118067 c.331G>T p.D111Y Substitution - Missense 23:154485803-154485803 - HCT15 COSM3034454 c.379C>A p.L127M Substitution - Missense 23:154485634-154485634 - HCT8 COSM3034454 c.379C>A p.L127M Substitution - Missense 23:154485634-154485634 - T407 COSM4738759 c.337A>T p.S113C Substitution - Missense 23:154485797-154485797 - TCGA-BK-A0CC-01 COSM1118070 c.265G>A p.D89N Substitution - Missense 23:154485869-154485869 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.76480 Xq28 312070

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G 3-UTRSNV . c.471+1527T>C X 153712354 HC C A Missense p.Q94H c.282G>T X 153714191 UCEC C A Missense p.R121M c.362G>T X 153714111 UCEC C T Missense p.D89N c.265G>A X 153714208 UCEC G A 3-UTRSNV . c.471+42C>T X 153713839 CM G A Missense p.R137W c.409C>T X 153713943 BLCA G A Missense p.S57L c.170C>T X 153714303 UCEC G - Frameshift p.P37Qfs*33 c.110delC X 153714611 RCCC