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 14 64954555 64954555 + Nonsense_Mutation SNP G G A TCGA-SY-A9G5-01A-11D-A38G-08 TCGA-SY-A9G5-10A-01D-A38J-08 g.chr14:64954555G>A c.394C>T c.(394-396)Cag>Tag p.Q132* BRCA 14 64954287 64954287 + Missense_Mutation SNP G G A TCGA-A2-A0EN-01A-13D-A099-09 TCGA-A2-A0EN-10A-01D-A099-09 g.chr14:64954287G>A c.662C>T c.(661-663)cCc>cTc p.P221L COAD 14 64954147 64954147 + Missense_Mutation SNP C C T TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr14:64954147C>T c.802G>A c.(802-804)Ggt>Agt p.G268S COAD 14 64954563 64954563 + Missense_Mutation SNP T T C TCGA-AY-4070-01A-01W-1073-09 TCGA-AY-4070-10A-01W-1073-09 g.chr14:64954563T>C c.386A>G c.(385-387)tAt>tGt p.Y129C COAD 14 64954668 64954668 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr14:64954668C>T c.281G>A c.(280-282)cGt>cAt p.R94H COADREAD 14 64954147 64954147 + Missense_Mutation SNP C C T TCGA-AD-6895-01A-11D-1924-10 TCGA-AD-6895-10A-01D-1924-10 g.chr14:64954147C>T c.802G>A c.(802-804)Ggt>Agt p.G268S COADREAD 14 64954563 64954563 + Missense_Mutation SNP T T C TCGA-AY-4070-01A-01W-1073-09 TCGA-AY-4070-10A-01W-1073-09 g.chr14:64954563T>C c.386A>G c.(385-387)tAt>tGt p.Y129C COADREAD 14 64954668 64954668 + Missense_Mutation SNP C C T TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr14:64954668C>T c.281G>A c.(280-282)cGt>cAt p.R94H ESCA 14 64953924 64953924 + Missense_Mutation SNP G G C TCGA-V5-AASX-01A-11D-A387-09 TCGA-V5-AASX-10A-01D-A38A-09 g.chr14:64953924G>C c.1025C>G c.(1024-1026)tCt>tGt p.S342C ESCA 14 64957115 64957115 + Missense_Mutation SNP G G T TCGA-JY-A93E-01A-11D-A37C-09 TCGA-JY-A93E-10A-01D-A37F-09 g.chr14:64957115G>T c.137C>A c.(136-138)tCt>tAt p.S46Y ESCA 14 64957175 64957175 + Missense_Mutation SNP C C T TCGA-V5-A7RB-01A-11D-A351-09 TCGA-V5-A7RB-10A-01D-A351-09 g.chr14:64957175C>T c.77G>A c.(76-78)tGc>tAc p.C26Y GBM 14 64953897 64953897 + Missense_Mutation SNP C C T TCGA-06-0649-01B-01W-0348-08 TCGA-06-0649-10A-01W-0348-08 g.chr14:64953897C>T c.1052G>A c.(1051-1053)tGt>tAt p.C351Y GBMLGG 14 64953897 64953897 + Missense_Mutation SNP C C T TCGA-06-0649-01B-01W-0348-08 TCGA-06-0649-10A-01W-0348-08 g.chr14:64953897C>T c.1052G>A c.(1051-1053)tGt>tAt p.C351Y HNSC 14 64954345 64954345 + Frame_Shift_Del DEL A A - TCGA-D6-6517-01A-11D-1870-08 TCGA-D6-6517-10A-01D-1870-08 g.chr14:64954345delA c.604delT c.(604-606)tccfs p.S202fs HNSC 14 64954378 64954378 + Nonsense_Mutation SNP G G A TCGA-CR-7374-01A-11D-2012-08 TCGA-CR-7374-10A-01D-2013-08 g.chr14:64954378G>A c.571C>T c.(571-573)Cag>Tag p.Q191* HNSC 14 64954651 64954651 + Nonsense_Mutation SNP G G A TCGA-CV-A45X-01A-21D-A25D-08 TCGA-CV-A45X-10A-01D-A25E-08 g.chr14:64954651G>A c.298C>T c.(298-300)Cga>Tga p.R100* KIPAN 14 64953924 64953924 + Missense_Mutation SNP G G T TCGA-B0-4819-01A-01D-1361-10 TCGA-B0-4819-11A-01D-1361-10 g.chr14:64953924G>T c.1025C>A c.(1024-1026)tCt>tAt p.S342Y KIPAN 14 64957106 64957106 + Frame_Shift_Del DEL A A - TCGA-SX-A7SS-01A-11D-A35Z-10 TCGA-SX-A7SS-10A-01D-A35Z-10 g.chr14:64957106delA c.146delT c.(145-147)ttcfs p.F49fs KIRC 14 64953924 64953924 + Missense_Mutation SNP G G T TCGA-B0-4819-01A-01D-1361-10 TCGA-B0-4819-11A-01D-1361-10 g.chr14:64953924G>T c.1025C>A c.(1024-1026)tCt>tAt p.S342Y KIRP 14 64957106 64957106 + Frame_Shift_Del DEL A A - TCGA-SX-A7SS-01A-11D-A35Z-10 TCGA-SX-A7SS-10A-01D-A35Z-10 g.chr14:64957106delA c.146delT c.(145-147)ttcfs p.F49fs LIHC 14 64954457 64954457 + Silent SNP G G A TCGA-DD-AAE4-01A-11D-A40R-10 TCGA-DD-AAE4-10A-01D-A40U-10 g.chr14:64954457G>A c.492C>T c.(490-492)gaC>gaT p.D164D LUAD 14 64953726 64953726 + Missense_Mutation SNP C C A TCGA-38-4631-01A-01D-1753-08 TCGA-38-4631-11A-01D-1753-08 g.chr14:64953726C>A c.1223G>T c.(1222-1224)cGc>cTc p.R408L LUAD 14 64954030 64954030 + Nonsense_Mutation SNP G G A TCGA-78-7155-01A-11D-2036-08 TCGA-78-7155-10A-01D-2036-08 g.chr14:64954030G>A c.919C>T c.(919-921)Cag>Tag p.Q307* LUAD 14 64954061 64954061 + Missense_Mutation SNP C C A TCGA-55-A4DG-01A-11D-A24D-08 TCGA-55-A4DG-10A-01D-A24F-08 g.chr14:64954061C>A c.888G>T c.(886-888)agG>agT p.R296S LUAD 14 64954403 64954403 + Missense_Mutation SNP G G C TCGA-55-8614-01A-11D-2393-08 TCGA-55-8614-10A-01D-2393-08 g.chr14:64954403G>C c.546C>G c.(544-546)gaC>gaG p.D182E LUAD 14 64954637 64954637 + Silent SNP G G A TCGA-55-7724-01A-11D-2167-08 TCGA-55-7724-10A-01D-2167-08 g.chr14:64954637G>A c.312C>T c.(310-312)gcC>gcT p.A104A LUAD 14 64957115 64957115 + Missense_Mutation SNP G G C TCGA-44-7662-01A-11D-2063-08 TCGA-44-7662-10A-01D-2063-08 g.chr14:64957115G>C c.137C>G c.(136-138)tCt>tGt p.S46C LUAD 14 64957119 64957119 + Missense_Mutation SNP A A G TCGA-95-7567-01A-11D-2063-08 TCGA-95-7567-10A-01D-2063-08 g.chr14:64957119A>G c.133T>C c.(133-135)Ttt>Ctt p.F45L OV 14 64954618 64954618 + Missense_Mutation SNP C C T TCGA-61-1907-01A-01W-0639-09 TCGA-61-1907-11A-01W-0640-09 g.chr14:64954618C>T c.331G>A c.(331-333)Gca>Aca p.A111T OV 14 64954742 64954742 + Missense_Mutation SNP T T G TCGA-25-2042-01A-01W-0799-08 TCGA-25-2042-10A-01W-0799-08 g.chr14:64954742T>G c.207A>C c.(205-207)caA>caC p.Q69H SKCM 14 64954158 64954158 + Missense_Mutation SNP G G A TCGA-FR-A3YO-06A-11D-A23B-08 TCGA-FR-A3YO-10A-01D-A23B-08 g.chr14:64954158G>A c.791C>T c.(790-792)tCc>tTc p.S264F SKCM 14 64954344 64954344 + Missense_Mutation SNP G G A TCGA-FS-A1Z3-06A-11D-A197-08 TCGA-FS-A1Z3-10A-01D-A199-08 g.chr14:64954344G>A c.605C>T c.(604-606)tCc>tTc p.S202F SKCM 14 64954352 64954352 + Silent SNP G G A TCGA-ER-A3EV-06A-11D-A20D-08 TCGA-ER-A3EV-10A-01D-A20D-08 g.chr14:64954352G>A c.597C>T c.(595-597)ccC>ccT p.P199P

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 14 64914970 64914970 single base substitution G C downstream_gene_variant BLCA-US 14 64921557 64921557 single base substitution C T intron_variant BLCA-US 14 64936344 64936344 single base substitution T G intron_variant BRCA-EU 14 64912036 64912036 single base substitution G C downstream_gene_variant BRCA-EU 14 64912884 64912884 single base substitution A T downstream_gene_variant BRCA-EU 14 64913592 64913592 single base substitution C T downstream_gene_variant BRCA-EU 14 64914574 64914574 single base substitution C T downstream_gene_variant BRCA-EU 14 64915533 64915533 single base substitution T G downstream_gene_variant BRCA-EU 14 64916140 64916140 single base substitution G C 3_prime_UTR_variant BRCA-EU 14 64916361 64916361 deletion of <=200bp A - intron_variant BRCA-EU 14 64918404 64918404 single base substitution T C intron_variant BRCA-EU 14 64921829 64921829 deletion of <=200bp A - intron_variant BRCA-EU 14 64922101 64922101 single base substitution G T intron_variant BRCA-EU 14 64926386 64926386 single base substitution A G intron_variant BRCA-EU 14 64926924 64926924 single base substitution G C intron_variant BRCA-EU 14 64926934 64926934 single base substitution G C intron_variant BRCA-EU 14 64926963 64926963 single base substitution C G intron_variant BRCA-EU 14 64927981 64927981 single base substitution A G intron_variant BRCA-EU 14 64928055 64928055 single base substitution G C intron_variant BRCA-EU 14 64928872 64928872 single base substitution G C intron_variant BRCA-EU 14 64931402 64931402 single base substitution A T intron_variant BRCA-EU 14 64935894 64935894 single base substitution T C intron_variant BRCA-EU 14 64936100 64936100 single base substitution G C intron_variant BRCA-EU 14 64936388 64936388 single base substitution C G intron_variant BRCA-EU 14 64936445 64936445 insertion of <=200bp - TT intron_variant BRCA-EU 14 64936483 64936483 single base substitution G C intron_variant BRCA-EU 14 64937164 64937164 single base substitution T C intron_variant BRCA-EU 14 64937262 64937262 single base substitution T C intron_variant BRCA-EU 14 64937686 64937686 single base substitution C T intron_variant BRCA-EU 14 64939256 64939256 single base substitution T G intron_variant BRCA-EU 14 64942639 64942639 single base substitution A T downstream_gene_variant BRCA-EU 14 64942639 64942639 single base substitution A T intron_variant BRCA-EU 14 64947518 64947518 single base substitution C T 3_prime_UTR_variant BRCA-EU 14 64947518 64947518 single base substitution C T intron_variant BRCA-EU 14 64947681 64947681 single base substitution C G 3_prime_UTR_variant BRCA-EU 14 64947681 64947681 single base substitution C G intron_variant BRCA-EU 14 64948202 64948202 single base substitution C A 3_prime_UTR_variant BRCA-EU 14 64948202 64948202 single base substitution C A intron_variant BRCA-EU 14 64952079 64952079 single base substitution G C 3_prime_UTR_variant BRCA-EU 14 64952079 64952079 single base substitution G C downstream_gene_variant BRCA-EU 14 64952079 64952079 single base substitution G C intron_variant BRCA-EU 14 64952416 64952416 single base substitution T C 3_prime_UTR_variant BRCA-EU 14 64952416 64952416 single base substitution T C downstream_gene_variant BRCA-EU 14 64952416 64952416 single base substitution T C intron_variant BRCA-EU 14 64953485 64953485 deletion of <=200bp T - 3_prime_UTR_variant BRCA-EU 14 64953485 64953485 deletion of <=200bp T - downstream_gene_variant BRCA-EU 14 64953485 64953485 deletion of <=200bp T - intron_variant BRCA-EU 14 64956540 64956540 single base substitution T A intron_variant BRCA-EU 14 64956744 64956744 single base substitution G A intron_variant BRCA-EU 14 64958005 64958005 single base substitution G T intron_variant BRCA-EU 14 64958005 64958005 single base substitution G T upstream_gene_variant BRCA-EU 14 64958964 64958964 single base substitution G C intron_variant BRCA-EU 14 64958964 64958964 single base substitution G C upstream_gene_variant BRCA-EU 14 64959567 64959567 insertion of <=200bp - A intron_variant BRCA-EU 14 64959567 64959567 insertion of <=200bp - A upstream_gene_variant BRCA-EU 14 64960537 64960537 single base substitution G C intron_variant BRCA-EU 14 64960537 64960537 single base substitution G C upstream_gene_variant BRCA-EU 14 64962176 64962176 single base substitution T C intron_variant BRCA-EU 14 64962176 64962176 single base substitution T C upstream_gene_variant BRCA-EU 14 64962619 64962619 single base substitution G C intron_variant BRCA-EU 14 64962622 64962622 single base substitution G T intron_variant BRCA-EU 14 64963209 64963209 deletion of <=200bp A - intron_variant BRCA-EU 14 64963451 64963451 single base substitution G A intron_variant BRCA-EU 14 64964330 64964330 single base substitution G C intron_variant BRCA-EU 14 64965021 64965021 single base substitution G C intron_variant BRCA-EU 14 64965270 64965270 single base substitution C T intron_variant BRCA-EU 14 64965382 64965382 single base substitution C T intron_variant BRCA-EU 14 64965437 64965437 single base substitution C T intron_variant BRCA-EU 14 64965494 64965494 single base substitution G A intron_variant BRCA-EU 14 64966074 64966074 single base substitution C T intron_variant BRCA-EU 14 64966185 64966185 single base substitution G A 5_prime_UTR_variant BRCA-EU 14 64966185 64966185 single base substitution G A intron_variant BRCA-EU 14 64968751 64968752 deletion of <=200bp TG - intron_variant BRCA-EU 14 64970320 64970320 single base substitution C G intron_variant BRCA-EU 14 64973146 64973146 single base substitution G C upstream_gene_variant BRCA-EU 14 64973658 64973658 single base substitution C T upstream_gene_variant BRCA-EU 14 64973693 64973693 single base substitution A G upstream_gene_variant BRCA-EU 14 64974230 64974230 single base substitution G A upstream_gene_variant BRCA-EU 14 64974361 64974361 single base substitution G T upstream_gene_variant BRCA-EU 14 64974742 64974742 single base substitution A T upstream_gene_variant BRCA-EU 14 64975043 64975043 single base substitution C A upstream_gene_variant BRCA-EU 14 64976588 64976588 single base substitution T G upstream_gene_variant BRCA-EU 14 64976747 64976747 single base substitution A C upstream_gene_variant BRCA-FR 14 64923126 64923126 single base substitution C G intron_variant BRCA-FR 14 64926924 64926924 single base substitution G C intron_variant BRCA-FR 14 64928055 64928055 single base substitution G C intron_variant BRCA-FR 14 64928872 64928872 single base substitution G C intron_variant BRCA-FR 14 64937686 64937686 single base substitution C T intron_variant BRCA-FR 14 64944108 64944108 single base substitution A T downstream_gene_variant BRCA-FR 14 64944108 64944108 single base substitution A T intron_variant BRCA-FR 14 64947681 64947681 single base substitution C G 3_prime_UTR_variant BRCA-FR 14 64947681 64947681 single base substitution C G intron_variant BRCA-FR 14 64950702 64950702 single base substitution G C 3_prime_UTR_variant BRCA-FR 14 64950702 64950702 single base substitution G C downstream_gene_variant BRCA-FR 14 64950702 64950702 single base substitution G C intron_variant BRCA-FR 14 64966185 64966185 single base substitution G A 5_prime_UTR_variant BRCA-FR 14 64966185 64966185 single base substitution G A intron_variant BRCA-FR 14 64971539 64971539 single base substitution G C 5_prime_UTR_premature_start_codon_gain_variant BRCA-FR 14 64971539 64971539 single base substitution G C upstream_gene_variant BRCA-FR 14 64973146 64973146 single base substitution G C upstream_gene_variant BRCA-US 14 64924931 64924931 single base substitution G A intron_variant BRCA-US 14 64935421 64935421 single base substitution T G intron_variant BRCA-US 14 64936324 64936324 single base substitution T A intron_variant BRCA-US 14 64954287 64954287 single base substitution G A intron_variant BRCA-US 14 64954287 64954287 single base substitution G A missense_variant P221L 662C>T BTCA-JP 14 64935816 64935816 single base substitution C T intron_variant BTCA-JP 14 64936422 64936422 single base substitution A T intron_variant BTCA-JP 14 64957201 64957201 single base substitution C T synonymous_variant Q17Q 51G>A BTCA-JP 14 64957305 64957305 single base substitution C T intron_variant BTCA-JP 14 64957305 64957305 single base substitution C T upstream_gene_variant CESC-US 14 64936170 64936170 single base substitution C T intron_variant CLLE-ES 14 64916959 64916959 single base substitution A G intron_variant CLLE-ES 14 64922013 64922013 insertion of <=200bp - A intron_variant CLLE-ES 14 64933109 64933109 single base substitution A G intron_variant CLLE-ES 14 64933162 64933162 single base substitution A G intron_variant CLLE-ES 14 64933165 64933165 single base substitution A C intron_variant CLLE-ES 14 64933246 64933246 single base substitution A G intron_variant CLLE-ES 14 64936833 64936833 single base substitution T C intron_variant CLLE-ES 14 64944612 64944612 single base substitution G C downstream_gene_variant CLLE-ES 14 64944612 64944612 single base substitution G C intron_variant CLLE-ES 14 64972196 64972196 single base substitution A G upstream_gene_variant CLLE-ES 14 64973313 64973313 single base substitution T G upstream_gene_variant COAD-US 14 64935339 64935339 deletion of <=200bp G - intron_variant COAD-US 14 64935817 64935817 single base substitution G A intron_variant COAD-US 14 64954147 64954147 single base substitution C T intron_variant COAD-US 14 64954147 64954147 single base substitution C T missense_variant G268S 802G>A COCA-CN 14 64911244 64911244 single base substitution C T downstream_gene_variant COCA-CN 14 64911343 64911343 single base substitution A T downstream_gene_variant COCA-CN 14 64926750 64926750 single base substitution C T intron_variant COCA-CN 14 64947068 64947068 single base substitution G A 3_prime_UTR_variant COCA-CN 14 64947068 64947068 single base substitution G A intron_variant COCA-CN 14 64953715 64953715 single base substitution C A intron_variant COCA-CN 14 64953715 64953715 single base substitution C A stop_gained E412* 1234G>T COCA-CN 14 64953943 64953943 single base substitution C A intron_variant COCA-CN 14 64953943 64953943 single base substitution C A stop_gained E336* 1006G>T EOPC-DE 14 64920763 64920763 single base substitution G C intron_variant ESAD-UK 14 64911822 64911822 single base substitution C G downstream_gene_variant ESAD-UK 14 64915534 64915534 insertion of <=200bp - G downstream_gene_variant ESAD-UK 14 64916942 64916942 single base substitution A T intron_variant ESAD-UK 14 64917621 64917621 single base substitution C T intron_variant ESAD-UK 14 64925899 64925925 deletion of <=200bp CTTCCTAAGAAGTTATTTAGCAATGTA - intron_variant ESAD-UK 14 64927486 64927486 single base substitution G A intron_variant ESAD-UK 14 64927645 64927645 single base substitution G A intron_variant ESAD-UK 14 64928550 64928550 single base substitution A G intron_variant ESAD-UK 14 64930263 64930263 single base substitution C G intron_variant ESAD-UK 14 64930660 64930660 single base substitution G A intron_variant ESAD-UK 14 64933303 64933303 single base substitution T G intron_variant ESAD-UK 14 64934028 64934028 single base substitution G A intron_variant ESAD-UK 14 64936255 64936255 single base substitution G A intron_variant ESAD-UK 14 64936256 64936256 single base substitution G T intron_variant ESAD-UK 14 64937824 64937824 single base substitution A G intron_variant ESAD-UK 14 64938597 64938597 single base substitution C A intron_variant ESAD-UK 14 64939124 64939124 deletion of <=200bp A - intron_variant ESAD-UK 14 64942074 64942074 single base substitution G A downstream_gene_variant ESAD-UK 14 64942074 64942074 single base substitution G A intron_variant ESAD-UK 14 64943716 64943716 single base substitution C T downstream_gene_variant ESAD-UK 14 64943716 64943716 single base substitution C T intron_variant ESAD-UK 14 64944258 64944258 single base substitution C T downstream_gene_variant ESAD-UK 14 64944258 64944258 single base substitution C T intron_variant ESAD-UK 14 64955722 64955722 single base substitution T C intron_variant ESAD-UK 14 64957713 64957713 single base substitution G A intron_variant ESAD-UK 14 64957713 64957713 single base substitution G A upstream_gene_variant ESAD-UK 14 64958957 64958957 single base substitution T A intron_variant ESAD-UK 14 64958957 64958957 single base substitution T A upstream_gene_variant ESAD-UK 14 64961521 64961521 single base substitution A C intron_variant ESAD-UK 14 64961521 64961521 single base substitution A C upstream_gene_variant ESAD-UK 14 64961684 64961684 single base substitution T G intron_variant ESAD-UK 14 64961684 64961684 single base substitution T G upstream_gene_variant ESAD-UK 14 64965104 64965104 single base substitution C T intron_variant ESAD-UK 14 64966083 64966083 single base substitution G A intron_variant ESAD-UK 14 64968078 64968078 single base substitution C T intron_variant ESAD-UK 14 64968581 64968581 single base substitution A G intron_variant ESAD-UK 14 64970306 64970316 deletion of <=200bp GCCGCCCTGGG - intron_variant ESAD-UK 14 64971056 64971056 single base substitution A G intron_variant ESAD-UK 14 64971056 64971056 single base substitution A G upstream_gene_variant ESAD-UK 14 64971088 64971088 insertion of <=200bp - GGG intron_variant ESAD-UK 14 64971088 64971088 insertion of <=200bp - GGG upstream_gene_variant ESAD-UK 14 64972973 64972973 single base substitution G A upstream_gene_variant ESCA-CN 14 64936142 64936142 single base substitution G A intron_variant ESCA-CN 14 64954305 64954305 single base substitution G C intron_variant ESCA-CN 14 64954305 64954305 single base substitution G C missense_variant S215C 644C>G GBM-US 14 64936331 64936331 single base substitution T C intron_variant GBM-US 14 64953897 64953897 single base substitution C T intron_variant GBM-US 14 64953897 64953897 single base substitution C T missense_variant C351Y 1052G>A GBM-US 14 64953897 64953897 single base substitution C T missense_variant C64Y 191G>A KIRC-US 14 64953924 64953924 single base substitution G T intron_variant KIRC-US 14 64953924 64953924 single base substitution G T missense_variant S342Y 1025C>A KIRP-US 14 64914978 64914979 deletion of <=200bp AA - downstream_gene_variant KIRP-US 14 64915025 64915025 single base substitution A C downstream_gene_variant KIRP-US 14 64924942 64924942 single base substitution T C intron_variant LAML-KR 14 64937328 64937328 single base substitution A G intron_variant LAML-KR 14 64947446 64947446 single base substitution G A 3_prime_UTR_variant LAML-KR 14 64947446 64947446 single base substitution G A intron_variant LAML-KR 14 64947447 64947447 single base substitution C T 3_prime_UTR_variant LAML-KR 14 64947447 64947447 single base substitution C T intron_variant LAML-KR 14 64947707 64947707 single base substitution A G 3_prime_UTR_variant LAML-KR 14 64947707 64947707 single base substitution A G intron_variant LAML-KR 14 64954683 64954683 single base substitution A G intron_variant LAML-KR 14 64954683 64954683 single base substitution A G missense_variant I89T 266T>C LGG-US 14 64936370 64936374 deletion of <=200bp AATAA - intron_variant LICA-FR 14 64935857 64935857 single base substitution C T intron_variant LICA-FR 14 64953902 64953902 single base substitution C A intron_variant LICA-FR 14 64953902 64953902 single base substitution C A missense_variant M349I 1047G>T LICA-FR 14 64953902 64953902 single base substitution C A missense_variant M62I 186G>T LIHC-US 14 64914955 64914955 single base substitution A G downstream_gene_variant LIHC-US 14 64954580 64954580 single base substitution C A intron_variant LIHC-US 14 64954580 64954580 single base substitution C A synonymous_variant V123V 369G>T LINC-JP 14 64912869 64912869 single base substitution A G downstream_gene_variant LINC-JP 14 64916361 64916361 insertion of <=200bp - A intron_variant LINC-JP 14 64917942 64917942 single base substitution A G intron_variant LINC-JP 14 64920095 64920095 single base substitution G A intron_variant LINC-JP 14 64920600 64920600 single base substitution T G intron_variant LINC-JP 14 64921361 64921361 single base substitution A G intron_variant LINC-JP 14 64944742 64944742 single base substitution C T downstream_gene_variant LINC-JP 14 64944742 64944742 single base substitution C T intron_variant LINC-JP 14 64953519 64953519 single base substitution C A 3_prime_UTR_variant LINC-JP 14 64953519 64953519 single base substitution C A downstream_gene_variant LINC-JP 14 64953519 64953519 single base substitution C A intron_variant LINC-JP 14 64953622 64953622 single base substitution A G 3_prime_UTR_variant LINC-JP 14 64953622 64953622 single base substitution A G intron_variant LINC-JP 14 64954716 64954716 single base substitution T C intron_variant LINC-JP 14 64954716 64954716 single base substitution T C missense_variant H78R 233A>G LINC-JP 14 64959637 64959637 single base substitution T C intron_variant LINC-JP 14 64959637 64959637 single base substitution T C upstream_gene_variant LINC-JP 14 64961006 64961006 single base substitution T C intron_variant LINC-JP 14 64961006 64961006 single base substitution T C upstream_gene_variant LINC-JP 14 64973295 64973295 single base substitution A G upstream_gene_variant LINC-JP 14 64976041 64976041 single base substitution A G upstream_gene_variant LIRI-JP 14 64910946 64910946 single base substitution G T downstream_gene_variant LIRI-JP 14 64913079 64913079 single base substitution A G downstream_gene_variant LIRI-JP 14 64913226 64913226 deletion of <=200bp T - downstream_gene_variant LIRI-JP 14 64913585 64913585 single base substitution A G downstream_gene_variant LIRI-JP 14 64915377 64915377 single base substitution G C downstream_gene_variant LIRI-JP 14 64915723 64915723 single base substitution T C downstream_gene_variant LIRI-JP 14 64916291 64916291 single base substitution A T 3_prime_UTR_variant LIRI-JP 14 64916291 64916291 single base substitution A T missense_variant L80Q 239T>A LIRI-JP 14 64918177 64918177 single base substitution A G intron_variant LIRI-JP 14 64920833 64920833 single base substitution C A intron_variant LIRI-JP 14 64921546 64921546 single base substitution A G intron_variant LIRI-JP 14 64922115 64922115 single base substitution G T intron_variant LIRI-JP 14 64925073 64925073 single base substitution A T intron_variant LIRI-JP 14 64925998 64925998 single base substitution A G intron_variant LIRI-JP 14 64926654 64926654 single base substitution A G intron_variant LIRI-JP 14 64927185 64927185 single base substitution G T intron_variant LIRI-JP 14 64927861 64927861 single base substitution A G intron_variant LIRI-JP 14 64928011 64928011 single base substitution A G intron_variant LIRI-JP 14 64928202 64928202 single base substitution G T intron_variant LIRI-JP 14 64929179 64929179 single base substitution A C intron_variant LIRI-JP 14 64930771 64930771 single base substitution A T intron_variant LIRI-JP 14 64930864 64930864 single base substitution T C intron_variant LIRI-JP 14 64933666 64933682 deletion of <=200bp ACTTATTTTTGGCTTTT - intron_variant LIRI-JP 14 64934048 64934048 single base substitution A C intron_variant LIRI-JP 14 64934076 64934076 single base substitution A C intron_variant LIRI-JP 14 64936697 64936697 single base substitution T C intron_variant LIRI-JP 14 64937830 64937830 single base substitution C A intron_variant LIRI-JP 14 64939575 64939575 single base substitution T C intron_variant LIRI-JP 14 64945133 64945133 single base substitution A G 3_prime_UTR_variant LIRI-JP 14 64945133 64945133 single base substitution A G intron_variant LIRI-JP 14 64946893 64946893 single base substitution T C 3_prime_UTR_variant LIRI-JP 14 64946893 64946893 single base substitution T C intron_variant LIRI-JP 14 64947837 64947837 single base substitution A G 3_prime_UTR_variant LIRI-JP 14 64947837 64947837 single base substitution A G intron_variant LIRI-JP 14 64948588 64948588 single base substitution T A 3_prime_UTR_variant LIRI-JP 14 64948588 64948588 single base substitution T A downstream_gene_variant LIRI-JP 14 64948588 64948588 single base substitution T A intron_variant LIRI-JP 14 64951760 64951771 deletion of <=200bp TTTACTCACTTG - 3_prime_UTR_variant LIRI-JP 14 64951760 64951771 deletion of <=200bp TTTACTCACTTG - downstream_gene_variant LIRI-JP 14 64951760 64951771 deletion of <=200bp TTTACTCACTTG - intron_variant LIRI-JP 14 64952115 64952115 single base substitution C A 3_prime_UTR_variant LIRI-JP 14 64952115 64952115 single base substitution C A downstream_gene_variant LIRI-JP 14 64952115 64952115 single base substitution C A intron_variant LIRI-JP 14 64956273 64956273 single base substitution A T intron_variant LIRI-JP 14 64956374 64956374 single base substitution C A intron_variant LIRI-JP 14 64956743 64956743 single base substitution T C intron_variant LIRI-JP 14 64958572 64958572 single base substitution T C intron_variant LIRI-JP 14 64958572 64958572 single base substitution T C upstream_gene_variant LIRI-JP 14 64962199 64962199 single base substitution T C intron_variant LIRI-JP 14 64962199 64962199 single base substitution T C upstream_gene_variant LIRI-JP 14 64968479 64968479 single base substitution G C intron_variant LIRI-JP 14 64968482 64968482 single base substitution C T intron_variant LIRI-JP 14 64968591 64968591 single base substitution C A intron_variant LIRI-JP 14 64968866 64968866 single base substitution A G intron_variant LIRI-JP 14 64975649 64975649 single base substitution G A upstream_gene_variant LUSC-KR 14 64912735 64912735 single base substitution G A downstream_gene_variant LUSC-KR 14 64914913 64914913 single base substitution C A downstream_gene_variant LUSC-KR 14 64922455 64922455 single base substitution G T intron_variant LUSC-KR 14 64925657 64925657 single base substitution G T intron_variant LUSC-KR 14 64952837 64952837 single base substitution G T 3_prime_UTR_variant LUSC-KR 14 64952837 64952837 single base substitution G T downstream_gene_variant LUSC-KR 14 64952837 64952837 single base substitution G T intron_variant LUSC-KR 14 64964049 64964049 single base substitution G C intron_variant LUSC-KR 14 64967193 64967193 single base substitution A G intron_variant LUSC-KR 14 64967446 64967446 single base substitution C T intron_variant LUSC-KR 14 64973536 64973536 single base substitution C T upstream_gene_variant LUSC-US 14 64921543 64921543 single base substitution G A intron_variant LUSC-US 14 64936211 64936211 single base substitution G C intron_variant MALY-DE 14 64912079 64912079 insertion of <=200bp - T downstream_gene_variant MALY-DE 14 64917170 64917170 single base substitution T C intron_variant MALY-DE 14 64926840 64926840 single base substitution C A intron_variant MALY-DE 14 64935471 64935471 single base substitution A G intron_variant MALY-DE 14 64951451 64951451 single base substitution A C 3_prime_UTR_variant MALY-DE 14 64951451 64951451 single base substitution A C downstream_gene_variant MALY-DE 14 64951451 64951451 single base substitution A C intron_variant MALY-DE 14 64958185 64958185 single base substitution A C intron_variant MALY-DE 14 64958185 64958185 single base substitution A C upstream_gene_variant MALY-DE 14 64958882 64958882 single base substitution T C intron_variant MALY-DE 14 64958882 64958882 single base substitution T C upstream_gene_variant MALY-DE 14 64962896 64962896 single base substitution C T intron_variant MALY-DE 14 64969983 64969983 single base substitution G A intron_variant MALY-DE 14 64971300 64971300 single base substitution C T 5_prime_UTR_variant MALY-DE 14 64971300 64971300 single base substitution C T upstream_gene_variant MALY-DE 14 64971653 64971653 single base substitution C T 5_prime_UTR_variant MALY-DE 14 64971653 64971653 single base substitution C T upstream_gene_variant MALY-DE 14 64971944 64971944 single base substitution T G upstream_gene_variant MALY-DE 14 64972696 64972696 single base substitution G A upstream_gene_variant MALY-DE 14 64975268 64975268 single base substitution T A upstream_gene_variant MALY-DE 14 64975528 64975528 single base substitution T C upstream_gene_variant MELA-AU 14 64912765 64912765 single base substitution C T downstream_gene_variant MELA-AU 14 64913046 64913046 single base substitution C T downstream_gene_variant MELA-AU 14 64914550 64914550 single base substitution C T downstream_gene_variant MELA-AU 14 64917347 64917347 single base substitution G A intron_variant MELA-AU 14 64917811 64917811 single base substitution C T intron_variant MELA-AU 14 64917936 64917936 single base substitution C T intron_variant MELA-AU 14 64918585 64918585 single base substitution C T intron_variant MELA-AU 14 64920921 64920921 single base substitution C T intron_variant MELA-AU 14 64921041 64921042 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 14 64923992 64923992 single base substitution C T intron_variant MELA-AU 14 64924607 64924607 single base substitution G A intron_variant MELA-AU 14 64924669 64924669 single base substitution G A intron_variant MELA-AU 14 64926810 64926810 single base substitution C T intron_variant MELA-AU 14 64928143 64928143 single base substitution C T intron_variant MELA-AU 14 64929531 64929531 single base substitution C T intron_variant MELA-AU 14 64930040 64930040 single base substitution T C intron_variant MELA-AU 14 64930064 64930065 deletion of <=200bp TG - intron_variant MELA-AU 14 64931558 64931559 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 14 64932361 64932362 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 14 64933422 64933422 single base substitution T C intron_variant MELA-AU 14 64933547 64933547 single base substitution G A intron_variant MELA-AU 14 64933893 64933893 single base substitution G A intron_variant MELA-AU 14 64934937 64934937 single base substitution G A intron_variant MELA-AU 14 64935957 64935957 single base substitution A G intron_variant MELA-AU 14 64936063 64936063 single base substitution T A intron_variant MELA-AU 14 64936586 64936586 single base substitution C T intron_variant MELA-AU 14 64936668 64936668 single base substitution G A intron_variant MELA-AU 14 64936791 64936791 single base substitution C T intron_variant MELA-AU 14 64937411 64937411 single base substitution C T intron_variant MELA-AU 14 64937516 64937516 single base substitution A T intron_variant MELA-AU 14 64938483 64938483 single base substitution G A intron_variant MELA-AU 14 64939701 64939701 single base substitution C T intron_variant MELA-AU 14 64940296 64940296 single base substitution A G downstream_gene_variant MELA-AU 14 64940296 64940296 single base substitution A G intron_variant MELA-AU 14 64940760 64940760 single base substitution G A downstream_gene_variant MELA-AU 14 64940760 64940760 single base substitution G A intron_variant MELA-AU 14 64942101 64942101 single base substitution G A downstream_gene_variant MELA-AU 14 64942101 64942101 single base substitution G A intron_variant MELA-AU 14 64943003 64943003 single base substitution G A downstream_gene_variant MELA-AU 14 64943003 64943003 single base substitution G A intron_variant MELA-AU 14 64943067 64943067 single base substitution G A downstream_gene_variant MELA-AU 14 64943067 64943067 single base substitution G A intron_variant MELA-AU 14 64943074 64943074 single base substitution C T downstream_gene_variant MELA-AU 14 64943074 64943074 single base substitution C T intron_variant MELA-AU 14 64943703 64943703 single base substitution A C downstream_gene_variant MELA-AU 14 64943703 64943703 single base substitution A C intron_variant MELA-AU 14 64944169 64944169 single base substitution G A downstream_gene_variant MELA-AU 14 64944169 64944169 single base substitution G A intron_variant MELA-AU 14 64944230 64944230 single base substitution G A downstream_gene_variant MELA-AU 14 64944230 64944230 single base substitution G A intron_variant MELA-AU 14 64944627 64944627 single base substitution G A downstream_gene_variant MELA-AU 14 64944627 64944627 single base substitution G A intron_variant MELA-AU 14 64945020 64945020 single base substitution G T 3_prime_UTR_variant MELA-AU 14 64945020 64945020 single base substitution G T intron_variant MELA-AU 14 64945036 64945036 single base substitution G C 3_prime_UTR_variant MELA-AU 14 64945036 64945036 single base substitution G C intron_variant MELA-AU 14 64945056 64945056 single base substitution G C 3_prime_UTR_variant MELA-AU 14 64945056 64945056 single base substitution G C intron_variant MELA-AU 14 64945373 64945373 single base substitution G C 3_prime_UTR_variant MELA-AU 14 64945373 64945373 single base substitution G C intron_variant MELA-AU 14 64945554 64945554 single base substitution G A 3_prime_UTR_variant MELA-AU 14 64945554 64945554 single base substitution G A intron_variant MELA-AU 14 64945644 64945644 single base substitution G C 3_prime_UTR_variant MELA-AU 14 64945644 64945644 single base substitution G C intron_variant MELA-AU 14 64946487 64946487 single base substitution G A 3_prime_UTR_variant MELA-AU 14 64946487 64946487 single base substitution G A intron_variant MELA-AU 14 64946700 64946700 single base substitution G A 3_prime_UTR_variant MELA-AU 14 64946700 64946700 single base substitution G A intron_variant MELA-AU 14 64946802 64946802 single base substitution G A 3_prime_UTR_variant MELA-AU 14 64946802 64946802 single base substitution G A intron_variant MELA-AU 14 64948790 64948790 single base substitution T C 3_prime_UTR_variant MELA-AU 14 64948790 64948790 single base substitution T C downstream_gene_variant MELA-AU 14 64948790 64948790 single base substitution T C intron_variant MELA-AU 14 64948834 64948834 single base substitution C T 3_prime_UTR_variant MELA-AU 14 64948834 64948834 single base substitution C T downstream_gene_variant MELA-AU 14 64948834 64948834 single base substitution C T intron_variant MELA-AU 14 64949388 64949388 single base substitution T A 3_prime_UTR_variant MELA-AU 14 64949388 64949388 single base substitution T A downstream_gene_variant MELA-AU 14 64949388 64949388 single base substitution T A intron_variant MELA-AU 14 64949635 64949635 single base substitution G A 3_prime_UTR_variant MELA-AU 14 64949635 64949635 single base substitution G A downstream_gene_variant MELA-AU 14 64949635 64949635 single base substitution G A intron_variant MELA-AU 14 64949809 64949809 single base substitution G A 3_prime_UTR_variant MELA-AU 14 64949809 64949809 single base substitution G A downstream_gene_variant MELA-AU 14 64949809 64949809 single base substitution G A intron_variant MELA-AU 14 64951159 64951159 single base substitution G A 3_prime_UTR_variant MELA-AU 14 64951159 64951159 single base substitution G A downstream_gene_variant MELA-AU 14 64951159 64951159 single base substitution G A intron_variant MELA-AU 14 64951386 64951386 single base substitution G A 3_prime_UTR_variant MELA-AU 14 64951386 64951386 single base substitution G A downstream_gene_variant MELA-AU 14 64951386 64951386 single base substitution G A intron_variant MELA-AU 14 64952382 64952382 single base substitution G A 3_prime_UTR_variant MELA-AU 14 64952382 64952382 single base substitution G A downstream_gene_variant MELA-AU 14 64952382 64952382 single base substitution G A intron_variant MELA-AU 14 64952947 64952947 single base substitution G A 3_prime_UTR_variant MELA-AU 14 64952947 64952947 single base substitution G A downstream_gene_variant MELA-AU 14 64952947 64952947 single base substitution G A intron_variant MELA-AU 14 64953602 64953602 insertion of <=200bp - T 3_prime_UTR_variant MELA-AU 14 64953602 64953602 insertion of <=200bp - T intron_variant MELA-AU 14 64954053 64954053 single base substitution G A intron_variant MELA-AU 14 64954053 64954053 single base substitution G A missense_variant S299F 896C>T MELA-AU 14 64955089 64955089 single base substitution G A intron_variant MELA-AU 14 64955536 64955536 single base substitution A G intron_variant MELA-AU 14 64956193 64956193 single base substitution G A intron_variant MELA-AU 14 64956200 64956200 single base substitution A T intron_variant MELA-AU 14 64956284 64956284 single base substitution C T intron_variant MELA-AU 14 64957086 64957086 single base substitution G A stop_gained Q56* 166C>T MELA-AU 14 64957947 64957947 single base substitution G A intron_variant MELA-AU 14 64957947 64957947 single base substitution G A upstream_gene_variant MELA-AU 14 64958048 64958048 single base substitution G A intron_variant MELA-AU 14 64958048 64958048 single base substitution G A upstream_gene_variant MELA-AU 14 64958904 64958904 single base substitution A T intron_variant MELA-AU 14 64958904 64958904 single base substitution A T upstream_gene_variant MELA-AU 14 64958947 64958948 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 14 64958947 64958948 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 14 64958983 64958983 single base substitution G A intron_variant MELA-AU 14 64958983 64958983 single base substitution G A upstream_gene_variant MELA-AU 14 64960503 64960503 single base substitution C T intron_variant MELA-AU 14 64960503 64960503 single base substitution C T upstream_gene_variant MELA-AU 14 64960796 64960796 single base substitution G A intron_variant MELA-AU 14 64960796 64960796 single base substitution G A upstream_gene_variant MELA-AU 14 64960843 64960843 single base substitution G C intron_variant MELA-AU 14 64960843 64960843 single base substitution G C upstream_gene_variant MELA-AU 14 64960961 64960961 single base substitution C G intron_variant MELA-AU 14 64960961 64960961 single base substitution C G upstream_gene_variant MELA-AU 14 64961014 64961014 single base substitution G A intron_variant MELA-AU 14 64961014 64961014 single base substitution G A upstream_gene_variant MELA-AU 14 64961026 64961026 single base substitution G A intron_variant MELA-AU 14 64961026 64961026 single base substitution G A upstream_gene_variant MELA-AU 14 64962032 64962032 single base substitution C T intron_variant MELA-AU 14 64962032 64962032 single base substitution C T upstream_gene_variant MELA-AU 14 64962102 64962102 single base substitution G A intron_variant MELA-AU 14 64962102 64962102 single base substitution G A upstream_gene_variant MELA-AU 14 64962679 64962679 single base substitution G A intron_variant MELA-AU 14 64962785 64962785 single base substitution G A intron_variant MELA-AU 14 64964204 64964204 single base substitution G A intron_variant MELA-AU 14 64965284 64965284 single base substitution C A intron_variant MELA-AU 14 64965734 64965734 single base substitution C T intron_variant MELA-AU 14 64967066 64967066 insertion of <=200bp - A intron_variant MELA-AU 14 64968551 64968551 single base substitution C A intron_variant MELA-AU 14 64970261 64970261 single base substitution C T intron_variant MELA-AU 14 64970951 64970951 single base substitution G A intron_variant MELA-AU 14 64970951 64970951 single base substitution G A upstream_gene_variant MELA-AU 14 64971483 64971483 single base substitution C T 5_prime_UTR_variant MELA-AU 14 64971483 64971483 single base substitution C T upstream_gene_variant MELA-AU 14 64972550 64972550 single base substitution C T upstream_gene_variant MELA-AU 14 64973711 64973711 single base substitution T C upstream_gene_variant MELA-AU 14 64976007 64976007 single base substitution G A upstream_gene_variant MELA-AU 14 64976196 64976196 single base substitution G C upstream_gene_variant MELA-AU 14 64976579 64976579 single base substitution C T upstream_gene_variant MELA-AU 14 64976657 64976657 single base substitution T G upstream_gene_variant ORCA-IN 14 64940736 64940736 single base substitution C T downstream_gene_variant ORCA-IN 14 64940736 64940736 single base substitution C T intron_variant ORCA-IN 14 64948757 64948757 single base substitution T G 3_prime_UTR_variant ORCA-IN 14 64948757 64948757 single base substitution T G downstream_gene_variant ORCA-IN 14 64948757 64948757 single base substitution T G intron_variant ORCA-IN 14 64954105 64954105 single base substitution C T intron_variant ORCA-IN 14 64954105 64954105 single base substitution C T missense_variant V282M 844G>A OV-AU 14 64911563 64911563 single base substitution G T downstream_gene_variant OV-AU 14 64918738 64918738 single base substitution G C intron_variant OV-AU 14 64940442 64940442 single base substitution A C downstream_gene_variant OV-AU 14 64940442 64940442 single base substitution A C intron_variant OV-AU 14 64946902 64946902 single base substitution G T 3_prime_UTR_variant OV-AU 14 64946902 64946902 single base substitution G T intron_variant OV-AU 14 64950830 64950830 single base substitution A G 3_prime_UTR_variant OV-AU 14 64950830 64950830 single base substitution A G downstream_gene_variant OV-AU 14 64950830 64950830 single base substitution A G intron_variant OV-AU 14 64960457 64960457 single base substitution T G intron_variant OV-AU 14 64960457 64960457 single base substitution T G upstream_gene_variant OV-AU 14 64968720 64968720 single base substitution C T intron_variant OV-AU 14 64972147 64972147 single base substitution C A upstream_gene_variant OV-AU 14 64973025 64973025 single base substitution T G upstream_gene_variant OV-AU 14 64974409 64974409 single base substitution C T upstream_gene_variant PACA-AU 14 64911850 64911852 deletion of <=200bp ATT - downstream_gene_variant PACA-AU 14 64913022 64913022 single base substitution C T downstream_gene_variant PACA-AU 14 64915533 64915533 single base substitution T G downstream_gene_variant PACA-AU 14 64917785 64917785 single base substitution G T intron_variant PACA-AU 14 64920608 64920608 single base substitution A T intron_variant PACA-AU 14 64935841 64935841 single base substitution A G intron_variant PACA-AU 14 64950322 64950322 single base substitution G A 3_prime_UTR_variant PACA-AU 14 64950322 64950322 single base substitution G A downstream_gene_variant PACA-AU 14 64950322 64950322 single base substitution G A intron_variant PACA-AU 14 64955556 64955556 single base substitution G A intron_variant PACA-AU 14 64958704 64958704 single base substitution G A intron_variant PACA-AU 14 64958704 64958704 single base substitution G A upstream_gene_variant PACA-CA 14 64915533 64915533 single base substitution T G downstream_gene_variant PACA-CA 14 64916674 64916674 single base substitution T A intron_variant PACA-CA 14 64918166 64918166 single base substitution A G intron_variant PACA-CA 14 64919026 64919026 single base substitution A G intron_variant PACA-CA 14 64925636 64925636 single base substitution T C intron_variant PACA-CA 14 64932423 64932423 single base substitution T C intron_variant PACA-CA 14 64933094 64933094 single base substitution G T intron_variant PACA-CA 14 64937614 64937614 single base substitution A G intron_variant PACA-CA 14 64938360 64938360 single base substitution G A intron_variant PACA-CA 14 64945688 64945688 insertion of <=200bp - AG 3_prime_UTR_variant PACA-CA 14 64945688 64945688 insertion of <=200bp - AG intron_variant PACA-CA 14 64952871 64952871 single base substitution T A 3_prime_UTR_variant PACA-CA 14 64952871 64952871 single base substitution T A downstream_gene_variant PACA-CA 14 64952871 64952871 single base substitution T A intron_variant PACA-CA 14 64953548 64953548 single base substitution A C 3_prime_UTR_variant PACA-CA 14 64953548 64953548 single base substitution A C downstream_gene_variant PACA-CA 14 64953548 64953548 single base substitution A C intron_variant PACA-CA 14 64954640 64954640 single base substitution G A intron_variant PACA-CA 14 64954640 64954640 single base substitution G A synonymous_variant H103H 309C>T PACA-CA 14 64959347 64959347 single base substitution G A intron_variant PACA-CA 14 64959347 64959347 single base substitution G A upstream_gene_variant PACA-CA 14 64962784 64962784 single base substitution C T intron_variant PACA-CA 14 64963356 64963356 single base substitution T A intron_variant PACA-CA 14 64971070 64971070 single base substitution T A intron_variant PACA-CA 14 64971070 64971070 single base substitution T A upstream_gene_variant PACA-CA 14 64971363 64971363 single base substitution G A 5_prime_UTR_variant PACA-CA 14 64971363 64971363 single base substitution G A upstream_gene_variant PACA-CA 14 64975363 64975363 single base substitution C A upstream_gene_variant PAEN-AU 14 64948630 64948630 single base substitution T G 3_prime_UTR_variant PAEN-AU 14 64948630 64948630 single base substitution T G downstream_gene_variant PAEN-AU 14 64948630 64948630 single base substitution T G intron_variant PAEN-AU 14 64949291 64949291 single base substitution A G 3_prime_UTR_variant PAEN-AU 14 64949291 64949291 single base substitution A G downstream_gene_variant PAEN-AU 14 64949291 64949291 single base substitution A G intron_variant PAEN-IT 14 64920411 64920411 single base substitution C A intron_variant PAEN-IT 14 64921553 64921553 single base substitution C T intron_variant PAEN-IT 14 64936072 64936072 single base substitution T C intron_variant PAEN-IT 14 64953155 64953155 single base substitution C A 3_prime_UTR_variant PAEN-IT 14 64953155 64953155 single base substitution C A downstream_gene_variant PAEN-IT 14 64953155 64953155 single base substitution C A intron_variant PBCA-DE 14 64912064 64912064 single base substitution T C downstream_gene_variant PBCA-DE 14 64928761 64928761 single base substitution C T intron_variant PBCA-DE 14 64950237 64950237 single base substitution C A 3_prime_UTR_variant PBCA-DE 14 64950237 64950237 single base substitution C A downstream_gene_variant PBCA-DE 14 64950237 64950237 single base substitution C A intron_variant PBCA-DE 14 64952727 64952727 insertion of <=200bp - T 3_prime_UTR_variant PBCA-DE 14 64952727 64952727 insertion of <=200bp - T downstream_gene_variant PBCA-DE 14 64952727 64952727 insertion of <=200bp - T intron_variant PBCA-DE 14 64956927 64956948 deletion of <=200bp AAAAAAAAAAAAAAAAAAAAAA - intron_variant PBCA-DE 14 64965659 64965659 insertion of <=200bp - T intron_variant PRAD-CA 14 64925681 64925681 single base substitution A C intron_variant PRAD-CA 14 64942991 64942991 single base substitution A G downstream_gene_variant PRAD-CA 14 64942991 64942991 single base substitution A G intron_variant PRAD-CA 14 64946270 64946270 single base substitution G C 3_prime_UTR_variant PRAD-CA 14 64946270 64946270 single base substitution G C intron_variant PRAD-UK 14 64922577 64922577 single base substitution C G intron_variant PRAD-UK 14 64941235 64941235 single base substitution C G downstream_gene_variant PRAD-UK 14 64941235 64941235 single base substitution C G intron_variant PRAD-UK 14 64947644 64947644 single base substitution C T 3_prime_UTR_variant PRAD-UK 14 64947644 64947644 single base substitution C T intron_variant PRAD-UK 14 64953516 64953516 single base substitution A C 3_prime_UTR_variant PRAD-UK 14 64953516 64953516 single base substitution A C downstream_gene_variant PRAD-UK 14 64953516 64953516 single base substitution A C intron_variant PRAD-UK 14 64956544 64956544 single base substitution G A intron_variant PRAD-UK 14 64960574 64960574 single base substitution A G intron_variant PRAD-UK 14 64960574 64960574 single base substitution A G upstream_gene_variant PRAD-UK 14 64963716 64963716 single base substitution A C intron_variant PRAD-UK 14 64970616 64970616 single base substitution C G intron_variant PRAD-UK 14 64970616 64970616 single base substitution C G upstream_gene_variant READ-US 14 64935520 64935520 deletion of <=200bp A - intron_variant RECA-EU 14 64926986 64926986 single base substitution A C intron_variant RECA-EU 14 64954340 64954340 single base substitution G T intron_variant RECA-EU 14 64954340 64954340 single base substitution G T synonymous_variant I203I 609C>A RECA-EU 14 64967193 64967193 single base substitution A G intron_variant SKCA-BR 14 64911081 64911081 single base substitution C T downstream_gene_variant SKCA-BR 14 64913669 64913669 single base substitution C T downstream_gene_variant SKCA-BR 14 64920642 64920642 single base substitution C G intron_variant SKCA-BR 14 64931704 64931704 single base substitution G A intron_variant SKCA-BR 14 64931929 64931929 single base substitution T C intron_variant SKCA-BR 14 64932109 64932109 single base substitution T C intron_variant SKCA-BR 14 64932129 64932129 single base substitution T C intron_variant SKCA-BR 14 64937352 64937352 single base substitution A G intron_variant SKCA-BR 14 64944797 64944797 single base substitution G A 3_prime_UTR_variant SKCA-BR 14 64944797 64944797 single base substitution G A intron_variant SKCA-BR 14 64947454 64947454 single base substitution G A 3_prime_UTR_variant SKCA-BR 14 64947454 64947454 single base substitution G A intron_variant SKCA-BR 14 64947808 64947808 insertion of <=200bp - TG 3_prime_UTR_variant SKCA-BR 14 64947808 64947808 insertion of <=200bp - TG intron_variant SKCA-BR 14 64948057 64948057 single base substitution G A 3_prime_UTR_variant SKCA-BR 14 64948057 64948057 single base substitution G A intron_variant SKCA-BR 14 64948673 64948673 single base substitution G A 3_prime_UTR_variant SKCA-BR 14 64948673 64948673 single base substitution G A downstream_gene_variant SKCA-BR 14 64948673 64948673 single base substitution G A intron_variant SKCA-BR 14 64950053 64950053 single base substitution T C 3_prime_UTR_variant SKCA-BR 14 64950053 64950053 single base substitution T C downstream_gene_variant SKCA-BR 14 64950053 64950053 single base substitution T C intron_variant SKCA-BR 14 64955671 64955671 single base substitution C T intron_variant SKCA-BR 14 64955689 64955689 single base substitution G A intron_variant SKCA-BR 14 64960562 64960562 insertion of <=200bp - CA intron_variant SKCA-BR 14 64960562 64960562 insertion of <=200bp - CA upstream_gene_variant SKCA-BR 14 64962679 64962679 single base substitution G A intron_variant SKCA-BR 14 64963839 64963839 single base substitution G A intron_variant SKCA-BR 14 64965912 64965912 single base substitution G A intron_variant SKCA-BR 14 64967193 64967193 insertion of <=200bp - AAAAG intron_variant SKCA-BR 14 64970470 64970470 single base substitution A C 5_prime_UTR_variant SKCA-BR 14 64970470 64970470 single base substitution A C intron_variant SKCA-BR 14 64972060 64972060 single base substitution T G upstream_gene_variant SKCA-BR 14 64972064 64972064 single base substitution A G upstream_gene_variant SKCA-BR 14 64972069 64972069 single base substitution A G upstream_gene_variant SKCA-BR 14 64973135 64973135 single base substitution C T upstream_gene_variant SKCA-BR 14 64974203 64974203 single base substitution A G upstream_gene_variant SKCM-US 14 64921587 64921587 single base substitution A T intron_variant SKCM-US 14 64935557 64935557 single base substitution G A intron_variant SKCM-US 14 64954158 64954158 single base substitution G A intron_variant SKCM-US 14 64954158 64954158 single base substitution G A missense_variant S264F 791C>T SKCM-US 14 64954344 64954344 single base substitution G A intron_variant SKCM-US 14 64954344 64954344 single base substitution G A missense_variant S202F 605C>T SKCM-US 14 64954352 64954352 single base substitution G A intron_variant SKCM-US 14 64954352 64954352 single base substitution G A synonymous_variant P199P 597C>T STAD-US 14 64915014 64915014 single base substitution T G downstream_gene_variant STAD-US 14 64921543 64921543 single base substitution G A intron_variant STAD-US 14 64935100 64935100 single base substitution G A intron_variant STAD-US 14 64935359 64935359 single base substitution A G intron_variant STAD-US 14 64935787 64935787 single base substitution G C intron_variant STAD-US 14 64936006 64936006 single base substitution G A intron_variant STAD-US 14 64953932 64953933 deletion of <=200bp AC - frameshift_variant C339 STAD-US 14 64953932 64953933 deletion of <=200bp AC - intron_variant STAD-US 14 64953979 64953979 single base substitution G A intron_variant STAD-US 14 64953979 64953979 single base substitution G A stop_gained Q324* 970C>T STAD-US 14 64954534 64954534 deletion of <=200bp T - frameshift_variant T139 STAD-US 14 64954534 64954534 deletion of <=200bp T - intron_variant STAD-US 14 64954669 64954669 single base substitution G A intron_variant STAD-US 14 64954669 64954669 single base substitution G A missense_variant R94C 280C>T UCEC-US 14 64915022 64915022 single base substitution G A downstream_gene_variant UCEC-US 14 64921540 64921540 single base substitution C T intron_variant UCEC-US 14 64921592 64921592 single base substitution C T intron_variant UCEC-US 14 64935406 64935406 single base substitution A C intron_variant UCEC-US 14 64935518 64935518 single base substitution C T intron_variant UCEC-US 14 64935975 64935975 single base substitution C A intron_variant UCEC-US 14 64953667 64953667 single base substitution T G intron_variant UCEC-US 14 64953667 64953667 single base substitution T G missense_variant N428H 1282A>C UCEC-US 14 64954122 64954122 single base substitution C T intron_variant UCEC-US 14 64954122 64954122 single base substitution C T missense_variant S276N 827G>A UCEC-US 14 64954376 64954376 single base substitution C A intron_variant UCEC-US 14 64954376 64954376 single base substitution C A missense_variant Q191H 573G>T UCEC-US 14 64954442 64954442 single base substitution C T intron_variant UCEC-US 14 64954442 64954442 single base substitution C T synonymous_variant Q169Q 507G>A UCEC-US 14 64954645 64954645 single base substitution G T intron_variant UCEC-US 14 64954645 64954645 single base substitution G T missense_variant L102I 304C>A UCEC-US 14 64954763 64954763 single base substitution T G intron_variant UCEC-US 14 64954763 64954763 single base substitution T G missense_variant K62N 186A>C

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand Pat_76_A COSM5848337 c.940C>T p.R314W Substitution - Missense 14:64487291-64487291 - TCGA-AX-A0J0-01 COSM957003 c.186A>C p.K62N Substitution - Missense 14:64488045-64488045 - Pat_45_B COSM5848338 c.8C>T p.T3I Substitution - Missense 14:64490526-64490526 - 2492725 COSM5725011 c.1074C>T p.F358F Substitution - coding silent 14:64487157-64487157 - TCGA-06-0649-01 COSM2151428 c.1052G>A p.C351Y Substitution - Missense 14:64487179-64487179 - U251 COSM1678058 c.886A>T p.R296W Substitution - Missense 14:64487345-64487345 - CHEWS029 COSM4577962 c.904G>A p.V302I Substitution - Missense 14:64487327-64487327 - 24T COSM108668 c.1025C>T p.S342F Substitution - Missense 14:64487206-64487206 - ESO-640 COSM1270709 c.309C>T p.H103H Substitution - coding silent 14:64487922-64487922 - 1517_CLM COSM5754605 c.574G>A p.A192T Substitution - Missense 14:64487657-64487657 - DLD1 COSM2248189 c.1257C>A p.A419A Substitution - coding silent 14:64486974-64486974 - HCT15 COSM2248189 c.1257C>A p.A419A Substitution - coding silent 14:64486974-64486974 - CHC258T COSM3667662 c.1047G>T p.M349I Substitution - Missense 14:64487184-64487184 - 2492724 COSM5725011 c.1074C>T p.F358F Substitution - coding silent 14:64487157-64487157 - TCGA-B0-4819-01 COSM3361195 c.1025C>A p.S342Y Substitution - Missense 14:64487206-64487206 - BICR_22 COSM2248190 c.1194C>G p.S398R Substitution - Missense 14:64487037-64487037 - TCGA-AA-A01P-01 COSM5121726 c.733_734insG p.E245fs*4 Insertion - Frameshift 14:64487497-64487498 - T636 COSM4742116 c.372G>A p.Q124Q Substitution - coding silent 14:64487859-64487859 - TCGA-AD-6895-01 COSM1370563 c.802G>A p.G268S Substitution - Missense 14:64487429-64487429 - CN-AML-08-T COSM5425606 c.266T>C p.I89T Substitution - Missense 14:64487965-64487965 - HCC132T COSM1607848 c.233A>G p.H78R Substitution - Missense 14:64487998-64487998 - PT44 COSM5926900 c.1075C>T p.P359S Substitution - Missense 14:64487156-64487156 - pfg100T COSM4747384 c.1210_1235del26 p.L404fs*23 Deletion - Frameshift 14:64486996-64487021 - TCGA-AX-A05Z-01 COSM956999 c.827G>A p.S276N Substitution - Missense 14:64487404-64487404 - C086 COSM5541918 c.642C>T p.I214I Substitution - coding silent 14:64487589-64487589 - TCGA-ER-A3EV-06 COSM3886207 c.597C>T p.P199P Substitution - coding silent 14:64487634-64487634 - TCGA-BR-4370-01 COSM115865 c.280C>T p.R94C Substitution - Missense 14:64487951-64487951 - TCGA-BR-8369-01 COSM4051805 c.970C>T p.Q324* Substitution - Nonsense 14:64487261-64487261 - LUAD-S01409 COSM346401 c.1106A>G p.Y369C Substitution - Missense 14:64487125-64487125 - LUAD-F00057 COSM339321 c.119C>T p.A40V Substitution - Missense 14:64490415-64490415 - CHC258T COSM3667662 c.1047G>T p.M349I Substitution - Missense 14:64487184-64487184 - TCGA-AP-A051-01 COSM957000 c.573G>T p.Q191H Substitution - Missense 14:64487658-64487658 - 14T COSM3711601 c.844G>A p.V282M Substitution - Missense 14:64487387-64487387 - SH-0622 COSM5017862 c.788delG p.G263fs*65 Deletion - Frameshift 14:64487443-64487443 - HCC132 COSM1607848 c.233A>G p.H78R Substitution - Missense 14:64487998-64487998 - ESO-081 COSM1243747 c.479C>T p.A160V Substitution - Missense 14:64487752-64487752 - TCGA-CC-A7II-01 COSM4937636 c.369G>T p.V123V Substitution - coding silent 14:64487862-64487862 - TCGA-BS-A0UV-01 COSM957002 c.304C>A p.L102I Substitution - Missense 14:64487927-64487927 - TCGA-06-0649 COSM2151428 c.1052G>A p.C351Y Substitution - Missense 14:64487179-64487179 - PA285 COSM1163062 c.238A>T p.M80L Substitution - Missense 14:64487993-64487993 - TCGA-AY-4070-01 COSM301337 c.386A>G p.Y129C Substitution - Missense 14:64487845-64487845 - OSCC-GB_00140111 COSM3711601 c.844G>A p.V282M Substitution - Missense 14:64487387-64487387 - Pat_76_B COSM5848337 c.940C>T p.R314W Substitution - Missense 14:64487291-64487291 - T2269 COSM4742115 c.1286T>G p.V429G Substitution - Missense 14:64486945-64486945 - C0050T COSM4150828 c.609C>A p.I203I Substitution - coding silent 14:64487622-64487622 - TCGA-AP-A056-01 COSM956998 c.1282A>C p.N428H Substitution - Missense 14:64486949-64486949 - ESCC-139T COSM3936578 c.644C>G p.S215C Substitution - Missense 14:64487587-64487587 - TCGA-FR-A3YO-06 COSM3497025 c.791C>T p.S264F Substitution - Missense 14:64487440-64487440 - TCGA-24-2280-01 COSM115865 c.280C>T p.R94C Substitution - Missense 14:64487951-64487951 - TCGA-A2-A0EN-01 COSM433246 c.662C>T p.P221L Substitution - Missense 14:64487569-64487569 - HOP-92 COSM1678058 c.886A>T p.R296W Substitution - Missense 14:64487345-64487345 - TCGA-61-1907-01 COSM1323442 c.331G>A p.A111T Substitution - Missense 14:64487900-64487900 - SNU-175 COSM2248199 c.719G>A p.C240Y Substitution - Missense 14:64487512-64487512 - TCGA-AP-A0LT-01 COSM957001 c.507G>A p.Q169Q Substitution - coding silent 14:64487724-64487724 - 2492726 COSM5725011 c.1074C>T p.F358F Substitution - coding silent 14:64487157-64487157 - cSCCP6 COSM136975 c.377C>T p.S126L Substitution - Missense 14:64487854-64487854 - PDA_032 COSM4999671 c.1142G>T p.C381F Substitution - Missense 14:64487089-64487089 - S0057 COSM5882526 c.85G>T p.A29S Substitution - Missense 14:64490449-64490449 - CN-AML-NR-08-Dx COSM5425606 c.266T>C p.I89T Substitution - Missense 14:64487965-64487965 - 102 COSM5015241 c.956C>G p.P319R Substitution - Missense 14:64487275-64487275 - 585276 COSM326902 c.868G>A p.E290K Substitution - Missense 14:64487363-64487363 - TCGA-WS-AB45-01 COSM5189865 c.867C>T p.S289S Substitution - coding silent 14:64487364-64487364 - 1517_PT COSM5754605 c.574G>A p.A192T Substitution - Missense 14:64487657-64487657 - BD124T COSM2248206 c.51G>A p.Q17Q Substitution - coding silent 14:64490483-64490483 - TCGA-FS-A1Z3-06 COSM3497026 c.605C>T p.S202F Substitution - Missense 14:64487626-64487626 - TCGA-25-2042-01 COSM73332 c.207A>C p.Q69H Substitution - Missense 14:64488024-64488024 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.654571 14q23-q24 194541

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A - Frameshift p.S202Pfs*12 c.604delT 14 64954345 HNSC C A Missense p.R408L c.1223G>T 14 64953726 LUAD C G Missense p.Q162H c.486G>C 14 64954463 CM C T Missense p.C351Y c.1052G>A 14 64953897 GBM C T Missense p.E290K c.868G>A 14 64954081 SCLC C T Missense p.R295H c.884G>A 14 64954065 STAD C T Synonymous p.Q169Q c.507G>A 14 64954442 UCEC G A Missense p.L292F c.874C>T 14 64954075 CM G A Missense p.P221L c.662C>T 14 64954287 BRCA G A Missense p.R94C c.280C>T 14 64954669 OV G A Missense p.R94C c.280C>T 14 64954669 STAD G A Missense p.S202F c.605C>T 14 64954344 CM G A Nonsense p.Q191* c.571C>T 14 64954378 CM G A Nonsense p.Q191* c.571C>T 14 64954378 HNSC G A Synonymous p.H103H c.309C>T 14 64954640 ESCA G A Synonymous p.P199P c.597C>T 14 64954352 CM G C Missense p.F358L c.1074C>G 14 64953875 MM G T Missense p.S342Y c.1025C>A 14 64953924 RCCC T C Missense p.Y129C c.386A>G 14 64954563 COREAD T G Missense p.Q69H c.207A>C 14 64954742 OV