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 4 39779392 39779392 + Frame_Shift_Del DEL A A - TCGA-DK-A3IU-01A-11D-A20D-08 TCGA-DK-A3IU-10A-01D-A20D-08 g.chr4:39779392delA c.490delA c.(490-492)aaafs p.K165fs BLCA 4 39779401 39779401 + Missense_Mutation SNP G G A TCGA-GU-A767-01A-11D-A32B-08 TCGA-GU-A767-10A-01D-A329-08 g.chr4:39779401G>A c.499G>A c.(499-501)Gaa>Aaa p.E167K COAD 4 39757280 39757280 + Missense_Mutation SNP C C T TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr4:39757280C>T c.220C>T c.(220-222)Cgg>Tgg p.R74W COAD 4 39776474 39776474 + Missense_Mutation SNP G G A TCGA-CK-5916-01A-11D-1650-10 TCGA-CK-5916-10A-01D-1650-10 g.chr4:39776474G>A c.320G>A c.(319-321)cGc>cAc p.R107H COAD 4 39779360 39779360 + Missense_Mutation SNP C C T TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr4:39779360C>T c.458C>T c.(457-459)gCt>gTt p.A153V COADREAD 4 39757280 39757280 + Missense_Mutation SNP C C T TCGA-AU-6004-01A-11D-1719-10 TCGA-AU-6004-10A-01D-1719-10 g.chr4:39757280C>T c.220C>T c.(220-222)Cgg>Tgg p.R74W COADREAD 4 39757308 39757308 + Missense_Mutation SNP A A G TCGA-AF-6655-01A-11D-1826-10 TCGA-AF-6655-10A-01D-1826-10 g.chr4:39757308A>G c.248A>G c.(247-249)aAt>aGt p.N83S COADREAD 4 39776474 39776474 + Missense_Mutation SNP G G A TCGA-CK-5916-01A-11D-1650-10 TCGA-CK-5916-10A-01D-1650-10 g.chr4:39776474G>A c.320G>A c.(319-321)cGc>cAc p.R107H COADREAD 4 39779360 39779360 + Missense_Mutation SNP C C T TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr4:39779360C>T c.458C>T c.(457-459)gCt>gTt p.A153V ESCA 4 39776478 39776478 + Silent SNP G G T TCGA-2H-A9GQ-01A-11D-A37C-09 TCGA-2H-A9GQ-11A-11D-A37F-09 g.chr4:39776478G>T c.324G>T c.(322-324)acG>acT p.T108T ESCA 4 39776500 39776500 + Missense_Mutation SNP C C G TCGA-LN-A9FO-01A-11D-A387-09 TCGA-LN-A9FO-10A-01D-A38A-09 g.chr4:39776500C>G c.346C>G c.(346-348)Cta>Gta p.L116V KIPAN 4 39757353 39757353 + Missense_Mutation SNP A A G TCGA-HE-A5NF-01A-11D-A26P-10 TCGA-HE-A5NF-10A-01D-A26P-10 g.chr4:39757353A>G c.293A>G c.(292-294)gAt>gGt p.D98G KIPAN 4 39779353 39779353 + Missense_Mutation SNP G G A TCGA-2Z-A9JG-01A-11D-A42J-10 TCGA-2Z-A9JG-10A-01D-A42M-10 g.chr4:39779353G>A c.451G>A c.(451-453)Gtg>Atg p.V151M KIRP 4 39757353 39757353 + Missense_Mutation SNP A A G TCGA-HE-A5NF-01A-11D-A26P-10 TCGA-HE-A5NF-10A-01D-A26P-10 g.chr4:39757353A>G c.293A>G c.(292-294)gAt>gGt p.D98G KIRP 4 39779353 39779353 + Missense_Mutation SNP G G A TCGA-2Z-A9JG-01A-11D-A42J-10 TCGA-2Z-A9JG-10A-01D-A42M-10 g.chr4:39779353G>A c.451G>A c.(451-453)Gtg>Atg p.V151M LIHC 4 39747379 39747379 + Missense_Mutation SNP A A T TCGA-G3-A3CG-01A-11D-A20W-10 TCGA-G3-A3CG-10A-01D-A20W-10 g.chr4:39747379A>T c.165A>T c.(163-165)agA>agT p.R55S LIHC 4 39780009 39780009 + Silent SNP A A G TCGA-ED-A4XI-01A-11D-A25V-10 TCGA-ED-A4XI-10A-01D-A25V-10 g.chr4:39780009A>G c.558A>G c.(556-558)aaA>aaG p.K186K LIHC 4 39780035 39780035 + Missense_Mutation SNP A A G TCGA-DD-AADW-01A-11D-A38X-10 TCGA-DD-AADW-10A-01D-A38X-10 g.chr4:39780035A>G c.584A>G c.(583-585)gAa>gGa p.E195G LUAD 4 39780016 39780016 + Missense_Mutation SNP G G A TCGA-05-4427-01A-21D-1855-08 TCGA-05-4427-10A-01D-1855-08 g.chr4:39780016G>A c.565G>A c.(565-567)Gat>Aat p.D189N OV 4 39747381 39747385 + Frame_Shift_Del DEL ACCAA ACCAA - TCGA-24-1469-01A-01W-0553-09 TCGA-24-1469-10A-01W-0553-09 g.chr4:39747381_39747385delACCAA c.167_171delACCAA c.(166-171)taccaafs p.YQ56fs OV 4 39779301 39779301 + Splice_Site SNP G G C TCGA-29-1776-01A-01W-0639-09 TCGA-29-1776-10A-01W-0639-09 g.chr4:39779301G>C c.e6-1 PAAD 4 39779392 39779392 + Frame_Shift_Del DEL A A - TCGA-3A-A9IV-01A-11D-A40W-08 TCGA-3A-A9IV-10A-01D-A40W-08 g.chr4:39779392delA c.490delA c.(490-492)aaafs p.K165fs READ 4 39757308 39757308 + Missense_Mutation SNP A A G TCGA-AF-6655-01A-11D-1826-10 TCGA-AF-6655-10A-01D-1826-10 g.chr4:39757308A>G c.248A>G c.(247-249)aAt>aGt p.N83S SKCM 4 39739109 39739109 + Missense_Mutation SNP G G A TCGA-EB-A5KH-06A-11D-A27K-08 TCGA-EB-A5KH-10A-01D-A27N-08 g.chr4:39739109G>A c.133G>A c.(133-135)Gga>Aga p.G45R SKCM 4 39757304 39757304 + Missense_Mutation SNP C C T TCGA-EE-A2MG-06A-11D-A197-08 TCGA-EE-A2MG-10A-01D-A199-08 g.chr4:39757304C>T c.244C>T c.(244-246)Cct>Tct p.P82S

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-US 4 39779392 39779392 deletion of <=200bp A - 3_prime_UTR_variant BLCA-US 4 39779392 39779392 deletion of <=200bp A - exon_variant BLCA-US 4 39779392 39779392 deletion of <=200bp A - frameshift_variant K103 BLCA-US 4 39779392 39779392 deletion of <=200bp A - frameshift_variant K113 BLCA-US 4 39779392 39779392 deletion of <=200bp A - frameshift_variant K164 BLCA-US 4 39779392 39779392 deletion of <=200bp A - intron_variant BRCA-EU 4 39696266 39696266 single base substitution G A upstream_gene_variant BRCA-EU 4 39696634 39696634 single base substitution C T upstream_gene_variant BRCA-EU 4 39698013 39698013 single base substitution A T upstream_gene_variant BRCA-EU 4 39698150 39698150 deletion of <=200bp T - upstream_gene_variant BRCA-EU 4 39698737 39698737 single base substitution C G upstream_gene_variant BRCA-EU 4 39699188 39699188 single base substitution C G upstream_gene_variant BRCA-EU 4 39699401 39699401 single base substitution G A upstream_gene_variant BRCA-EU 4 39700578 39700578 single base substitution G A intron_variant BRCA-EU 4 39700633 39700633 single base substitution T C intron_variant BRCA-EU 4 39704570 39704570 single base substitution C T intron_variant BRCA-EU 4 39706358 39706358 single base substitution C T intron_variant BRCA-EU 4 39706660 39706660 insertion of <=200bp - T intron_variant BRCA-EU 4 39706670 39706670 deletion of <=200bp T - intron_variant BRCA-EU 4 39706750 39706751 deletion of <=200bp CT - intron_variant BRCA-EU 4 39707724 39707724 single base substitution C T intron_variant BRCA-EU 4 39709677 39709677 single base substitution C T intron_variant BRCA-EU 4 39709683 39709683 single base substitution A G intron_variant BRCA-EU 4 39710779 39710779 single base substitution G C intron_variant BRCA-EU 4 39710963 39710963 single base substitution C G intron_variant BRCA-EU 4 39711448 39711448 single base substitution G A intron_variant BRCA-EU 4 39713129 39713129 single base substitution T A intron_variant BRCA-EU 4 39713243 39713243 single base substitution G A intron_variant BRCA-EU 4 39714589 39714589 single base substitution G T intron_variant BRCA-EU 4 39715057 39715057 insertion of <=200bp - C intron_variant BRCA-EU 4 39715422 39715422 single base substitution T A intron_variant BRCA-EU 4 39715423 39715423 single base substitution A G intron_variant BRCA-EU 4 39715624 39715624 single base substitution C A intron_variant BRCA-EU 4 39716806 39716806 single base substitution C G intron_variant BRCA-EU 4 39716967 39716967 single base substitution T A intron_variant BRCA-EU 4 39717463 39717463 single base substitution T G intron_variant BRCA-EU 4 39718769 39718769 single base substitution C A intron_variant BRCA-EU 4 39719634 39719634 single base substitution C T intron_variant BRCA-EU 4 39721955 39721955 deletion of <=200bp C - intron_variant BRCA-EU 4 39722607 39722607 single base substitution T A intron_variant BRCA-EU 4 39722691 39722691 single base substitution C T intron_variant BRCA-EU 4 39722692 39722692 single base substitution C T intron_variant BRCA-EU 4 39723748 39723748 insertion of <=200bp - A intron_variant BRCA-EU 4 39724831 39724831 single base substitution T A intron_variant BRCA-EU 4 39727280 39727280 single base substitution G A intron_variant BRCA-EU 4 39728345 39728345 single base substitution A C intron_variant BRCA-EU 4 39732242 39732242 single base substitution G C intron_variant BRCA-EU 4 39732743 39732743 single base substitution C T intron_variant BRCA-EU 4 39735284 39735284 single base substitution G C intron_variant BRCA-EU 4 39736682 39736682 single base substitution A T intron_variant BRCA-EU 4 39736966 39736966 single base substitution C G intron_variant BRCA-EU 4 39737886 39737886 single base substitution G A intron_variant BRCA-EU 4 39739054 39739054 single base substitution A G exon_variant BRCA-EU 4 39739054 39739054 single base substitution A G intron_variant BRCA-EU 4 39739054 39739054 single base substitution A G synonymous_variant Q26Q 78A>G BRCA-EU 4 39740492 39740492 single base substitution A C intron_variant BRCA-EU 4 39741796 39741796 deletion of <=200bp T - intron_variant BRCA-EU 4 39742343 39742343 single base substitution C T intron_variant BRCA-EU 4 39742630 39742630 single base substitution T A intron_variant BRCA-EU 4 39743405 39743405 single base substitution A C intron_variant BRCA-EU 4 39744717 39744717 single base substitution G C intron_variant BRCA-EU 4 39744887 39744887 deletion of <=200bp T - intron_variant BRCA-EU 4 39745254 39745254 single base substitution T A intron_variant BRCA-EU 4 39745334 39745334 single base substitution C T intron_variant BRCA-EU 4 39746409 39746409 single base substitution C T intron_variant BRCA-EU 4 39747185 39747185 single base substitution C T intron_variant BRCA-EU 4 39751829 39751829 insertion of <=200bp - A intron_variant BRCA-EU 4 39753200 39753200 single base substitution G A intron_variant BRCA-EU 4 39753246 39753246 single base substitution G C intron_variant BRCA-EU 4 39754401 39754401 single base substitution A G intron_variant BRCA-EU 4 39758248 39758248 deletion of <=200bp T - intron_variant BRCA-EU 4 39758762 39758762 single base substitution T C intron_variant BRCA-EU 4 39760422 39760436 deletion of <=200bp AAGATTATGGTGTGT - intron_variant BRCA-EU 4 39760906 39760906 insertion of <=200bp - T intron_variant BRCA-EU 4 39760972 39760972 single base substitution C T intron_variant BRCA-EU 4 39762604 39762604 deletion of <=200bp A - intron_variant BRCA-EU 4 39763472 39763472 single base substitution A G intron_variant BRCA-EU 4 39763656 39763656 single base substitution G A intron_variant BRCA-EU 4 39765383 39765383 insertion of <=200bp - T intron_variant BRCA-EU 4 39770232 39770232 single base substitution G A intron_variant BRCA-EU 4 39772143 39772143 single base substitution G A intron_variant BRCA-EU 4 39773843 39773843 single base substitution C T intron_variant BRCA-EU 4 39774330 39774330 single base substitution T C intron_variant BRCA-EU 4 39775323 39775371 multiple base substitution (>=2bp and <=200bp) CGAGGTCAGGAGATCGAGACCATCCTGGCTAACACAGTGAAACCCCGTC CAAGGTCAGGAGATCAAGACCATCCTGTGTCTCACGGTGAAACCCTGT intron_variant BRCA-EU 4 39776790 39776790 single base substitution C G intron_variant BRCA-EU 4 39776881 39776881 single base substitution C G intron_variant BRCA-EU 4 39780874 39780874 single base substitution A G 3_prime_UTR_variant BRCA-EU 4 39780874 39780874 single base substitution A G downstream_gene_variant BRCA-EU 4 39780874 39780874 single base substitution A G exon_variant BRCA-EU 4 39781302 39781302 single base substitution A G 3_prime_UTR_variant BRCA-EU 4 39781302 39781302 single base substitution A G downstream_gene_variant BRCA-EU 4 39781302 39781302 single base substitution A G exon_variant BRCA-EU 4 39785027 39785027 single base substitution T A downstream_gene_variant BRCA-EU 4 39785091 39785091 single base substitution G A downstream_gene_variant BRCA-EU 4 39785361 39785361 single base substitution G A downstream_gene_variant BRCA-EU 4 39785586 39785586 single base substitution A G downstream_gene_variant BRCA-EU 4 39786319 39786319 single base substitution C T downstream_gene_variant BRCA-EU 4 39787698 39787698 single base substitution A T downstream_gene_variant BRCA-EU 4 39787772 39787772 single base substitution A G downstream_gene_variant BRCA-EU 4 39787848 39787848 single base substitution C G downstream_gene_variant BRCA-EU 4 39789244 39789244 single base substitution G C downstream_gene_variant BRCA-FR 4 39698737 39698737 single base substitution C G upstream_gene_variant BRCA-FR 4 39699188 39699188 single base substitution C G upstream_gene_variant BRCA-FR 4 39716967 39716967 single base substitution T A intron_variant BRCA-FR 4 39737700 39737700 single base substitution A G intron_variant BRCA-FR 4 39746409 39746409 single base substitution C T intron_variant BRCA-FR 4 39747185 39747185 single base substitution C T intron_variant BRCA-FR 4 39758161 39758161 single base substitution C A intron_variant BRCA-FR 4 39760972 39760972 single base substitution C T intron_variant BRCA-FR 4 39762915 39762915 single base substitution C T intron_variant BRCA-FR 4 39767249 39767249 single base substitution G T intron_variant BRCA-FR 4 39776881 39776881 single base substitution C G intron_variant BRCA-FR 4 39787848 39787848 single base substitution C G downstream_gene_variant BRCA-FR 4 39789244 39789244 single base substitution G C downstream_gene_variant BRCA-UK 4 39698013 39698013 single base substitution A T upstream_gene_variant BRCA-UK 4 39737886 39737886 single base substitution G A intron_variant BRCA-UK 4 39787772 39787772 single base substitution A G downstream_gene_variant CLLE-ES 4 39697524 39697524 single base substitution T C upstream_gene_variant CLLE-ES 4 39707692 39707692 single base substitution C T intron_variant CLLE-ES 4 39714480 39714480 single base substitution A T intron_variant CLLE-ES 4 39772906 39772906 single base substitution A G intron_variant CLLE-ES 4 39784689 39784689 single base substitution G A downstream_gene_variant COAD-US 4 39757280 39757280 single base substitution C T exon_variant COAD-US 4 39757280 39757280 single base substitution C T intron_variant COAD-US 4 39757280 39757280 single base substitution C T missense_variant R23W 67C>T COAD-US 4 39757280 39757280 single base substitution C T missense_variant R74W 220C>T COAD-US 4 39776474 39776474 single base substitution G A exon_variant COAD-US 4 39776474 39776474 single base substitution G A intron_variant COAD-US 4 39776474 39776474 single base substitution G A missense_variant R107H 320G>A COAD-US 4 39776474 39776474 single base substitution G A missense_variant R56H 167G>A COAD-US 4 39779360 39779360 single base substitution C T 3_prime_UTR_variant COAD-US 4 39779360 39779360 single base substitution C T exon_variant COAD-US 4 39779360 39779360 single base substitution C T intron_variant COAD-US 4 39779360 39779360 single base substitution C T missense_variant A102V 305C>T COAD-US 4 39779360 39779360 single base substitution C T missense_variant A153V 458C>T COAD-US 4 39779360 39779360 single base substitution C T missense_variant A92V 275C>T COCA-CN 4 39742547 39742547 single base substitution C T intron_variant COCA-CN 4 39742552 39742552 single base substitution C T intron_variant COCA-CN 4 39767562 39767562 single base substitution C T intron_variant COCA-CN 4 39771936 39771936 single base substitution C T intron_variant COCA-CN 4 39772064 39772064 single base substitution C T intron_variant COCA-CN 4 39772524 39772524 single base substitution C T intron_variant COCA-CN 4 39780140 39780140 single base substitution C A 3_prime_UTR_variant COCA-CN 4 39780140 39780140 single base substitution C A downstream_gene_variant COCA-CN 4 39780140 39780140 single base substitution C A exon_variant EOPC-DE 4 39712660 39712660 single base substitution G T intron_variant EOPC-DE 4 39755141 39755141 single base substitution G A intron_variant ESAD-UK 4 39696816 39696816 single base substitution C T upstream_gene_variant ESAD-UK 4 39703640 39703640 single base substitution C G intron_variant ESAD-UK 4 39708034 39708034 single base substitution T C intron_variant ESAD-UK 4 39708694 39708694 deletion of <=200bp T - intron_variant ESAD-UK 4 39712809 39712809 single base substitution G A intron_variant ESAD-UK 4 39714475 39714475 single base substitution T G intron_variant ESAD-UK 4 39716106 39716106 single base substitution C T intron_variant ESAD-UK 4 39716391 39716391 single base substitution G A intron_variant ESAD-UK 4 39717942 39717942 single base substitution G A intron_variant ESAD-UK 4 39717972 39717972 single base substitution A C intron_variant ESAD-UK 4 39720471 39720471 single base substitution C T intron_variant ESAD-UK 4 39726673 39726673 single base substitution A T intron_variant ESAD-UK 4 39727571 39727571 single base substitution T A intron_variant ESAD-UK 4 39729286 39729286 single base substitution C A intron_variant ESAD-UK 4 39730276 39730276 single base substitution G A intron_variant ESAD-UK 4 39730664 39730664 single base substitution C G intron_variant ESAD-UK 4 39733171 39733171 single base substitution G A intron_variant ESAD-UK 4 39736157 39736157 single base substitution C T intron_variant ESAD-UK 4 39736597 39736597 single base substitution T C intron_variant ESAD-UK 4 39737502 39737502 single base substitution T G intron_variant ESAD-UK 4 39738473 39738473 single base substitution T G intron_variant ESAD-UK 4 39738869 39738869 insertion of <=200bp - T intron_variant ESAD-UK 4 39740409 39740409 single base substitution T A intron_variant ESAD-UK 4 39741582 39741582 insertion of <=200bp - T intron_variant ESAD-UK 4 39745894 39745894 single base substitution G A intron_variant ESAD-UK 4 39746551 39746551 deletion of <=200bp A - intron_variant ESAD-UK 4 39746582 39746582 single base substitution A G intron_variant ESAD-UK 4 39751808 39751808 single base substitution C T intron_variant ESAD-UK 4 39754976 39754976 deletion of <=200bp A - intron_variant ESAD-UK 4 39755049 39755049 single base substitution T G intron_variant ESAD-UK 4 39756024 39756024 single base substitution G C intron_variant ESAD-UK 4 39757149 39757149 single base substitution C T intron_variant ESAD-UK 4 39757185 39757185 deletion of <=200bp T - intron_variant ESAD-UK 4 39759971 39759971 single base substitution G A intron_variant ESAD-UK 4 39762027 39762027 single base substitution G A intron_variant ESAD-UK 4 39762987 39762987 single base substitution C T intron_variant ESAD-UK 4 39764667 39764667 single base substitution G A intron_variant ESAD-UK 4 39765059 39765059 single base substitution C T intron_variant ESAD-UK 4 39766828 39766828 single base substitution T A intron_variant ESAD-UK 4 39767067 39767067 single base substitution T G intron_variant ESAD-UK 4 39770000 39770000 single base substitution A G intron_variant ESAD-UK 4 39771425 39771425 single base substitution C T intron_variant ESAD-UK 4 39772310 39772310 single base substitution C A intron_variant ESAD-UK 4 39775754 39775754 single base substitution G A intron_variant ESAD-UK 4 39776323 39776323 single base substitution T G intron_variant ESAD-UK 4 39777371 39777371 single base substitution C T intron_variant ESAD-UK 4 39786479 39786479 single base substitution G C downstream_gene_variant ESAD-UK 4 39788298 39788298 single base substitution G A downstream_gene_variant KIRP-US 4 39757353 39757353 single base substitution A G exon_variant KIRP-US 4 39757353 39757353 single base substitution A G intron_variant KIRP-US 4 39757353 39757353 single base substitution A G missense_variant D47G 140A>G KIRP-US 4 39757353 39757353 single base substitution A G missense_variant D98G 293A>G LAML-KR 4 39727016 39727016 single base substitution A C intron_variant LAML-KR 4 39767209 39767209 single base substitution A G intron_variant LAML-KR 4 39767210 39767210 single base substitution T C intron_variant LICA-FR 4 39694982 39694982 single base substitution G A upstream_gene_variant LICA-FR 4 39699198 39699198 single base substitution C T upstream_gene_variant LICA-FR 4 39703463 39703463 single base substitution C T intron_variant LICA-FR 4 39716967 39716967 single base substitution T A intron_variant LICA-FR 4 39737297 39737297 single base substitution G A intron_variant LICA-FR 4 39741236 39741236 single base substitution T A intron_variant LICA-FR 4 39741334 39741334 single base substitution A G intron_variant LICA-FR 4 39741344 39741344 single base substitution C T intron_variant LICA-FR 4 39743307 39743307 single base substitution A G intron_variant LICA-FR 4 39763072 39763072 single base substitution A G intron_variant LICA-FR 4 39770384 39770384 single base substitution G A intron_variant LIHC-US 4 39780009 39780009 single base substitution A G 3_prime_UTR_variant LIHC-US 4 39780009 39780009 single base substitution A G downstream_gene_variant LIHC-US 4 39780009 39780009 single base substitution A G exon_variant LIHC-US 4 39780009 39780009 single base substitution A G synonymous_variant K125K 375A>G LIHC-US 4 39780009 39780009 single base substitution A G synonymous_variant K135K 405A>G LIHC-US 4 39780009 39780009 single base substitution A G synonymous_variant K143K 429A>G LIHC-US 4 39780009 39780009 single base substitution A G synonymous_variant K186K 558A>G LINC-JP 4 39700379 39700379 single base substitution G A intron_variant LINC-JP 4 39703896 39703896 single base substitution C A intron_variant LINC-JP 4 39714499 39714499 single base substitution T A intron_variant LINC-JP 4 39715229 39715229 single base substitution A G intron_variant LINC-JP 4 39729891 39729891 single base substitution T C intron_variant LINC-JP 4 39737644 39737644 single base substitution T G intron_variant LINC-JP 4 39739064 39739066 deletion of <=200bp GAT - exon_variant LINC-JP 4 39739064 39739066 deletion of <=200bp GAT - inframe_deletion D30 LINC-JP 4 39739064 39739066 deletion of <=200bp GAT - intron_variant LINC-JP 4 39772460 39772460 single base substitution C T intron_variant LINC-JP 4 39776683 39776683 single base substitution T C intron_variant LINC-JP 4 39779199 39779199 single base substitution A T intron_variant LINC-JP 4 39779461 39779461 single base substitution A G intron_variant LINC-JP 4 39780677 39780677 single base substitution G C 3_prime_UTR_variant LINC-JP 4 39780677 39780677 single base substitution G C downstream_gene_variant LINC-JP 4 39780677 39780677 single base substitution G C exon_variant LINC-JP 4 39787198 39787198 single base substitution C T downstream_gene_variant LIRI-JP 4 39703293 39703294 deletion of <=200bp AC - intron_variant LIRI-JP 4 39703822 39703822 single base substitution T C intron_variant LIRI-JP 4 39704289 39704289 single base substitution T G intron_variant LIRI-JP 4 39705026 39705026 single base substitution C T intron_variant LIRI-JP 4 39708128 39708128 single base substitution T G intron_variant LIRI-JP 4 39709559 39709559 single base substitution C G intron_variant LIRI-JP 4 39710583 39710583 single base substitution C G intron_variant LIRI-JP 4 39714089 39714089 single base substitution G A intron_variant LIRI-JP 4 39714370 39714370 single base substitution A G intron_variant LIRI-JP 4 39715491 39715491 single base substitution A G intron_variant LIRI-JP 4 39715620 39715620 single base substitution C A intron_variant LIRI-JP 4 39716041 39716041 single base substitution G A intron_variant LIRI-JP 4 39716736 39716736 single base substitution C T intron_variant LIRI-JP 4 39716871 39716871 single base substitution A G intron_variant LIRI-JP 4 39717238 39717238 insertion of <=200bp - T intron_variant LIRI-JP 4 39717479 39717479 single base substitution T A intron_variant LIRI-JP 4 39717739 39717739 single base substitution A G intron_variant LIRI-JP 4 39719073 39719073 single base substitution A G intron_variant LIRI-JP 4 39719293 39719293 single base substitution A G intron_variant LIRI-JP 4 39721405 39721405 single base substitution T A intron_variant LIRI-JP 4 39725415 39725415 single base substitution A G intron_variant LIRI-JP 4 39725503 39725503 single base substitution G T intron_variant LIRI-JP 4 39725580 39725580 single base substitution A G intron_variant LIRI-JP 4 39730407 39730407 single base substitution C T intron_variant LIRI-JP 4 39730577 39730577 single base substitution G A intron_variant LIRI-JP 4 39730897 39730897 single base substitution A G intron_variant LIRI-JP 4 39732674 39732674 single base substitution C T intron_variant LIRI-JP 4 39734471 39734471 single base substitution T C intron_variant LIRI-JP 4 39736800 39736800 single base substitution A G intron_variant LIRI-JP 4 39737391 39737391 single base substitution A G intron_variant LIRI-JP 4 39738416 39738416 single base substitution A G intron_variant LIRI-JP 4 39739775 39739775 single base substitution A G intron_variant LIRI-JP 4 39740604 39740604 single base substitution A G intron_variant LIRI-JP 4 39743949 39743949 single base substitution C T intron_variant LIRI-JP 4 39746867 39746867 single base substitution G A intron_variant LIRI-JP 4 39746868 39746868 single base substitution C T intron_variant LIRI-JP 4 39750747 39750747 single base substitution A G intron_variant LIRI-JP 4 39751326 39751326 single base substitution T C intron_variant LIRI-JP 4 39751441 39751441 single base substitution A G intron_variant LIRI-JP 4 39752601 39752601 single base substitution G T intron_variant LIRI-JP 4 39753038 39753038 single base substitution A G intron_variant LIRI-JP 4 39753070 39753070 single base substitution A G intron_variant LIRI-JP 4 39754342 39754342 single base substitution A G intron_variant LIRI-JP 4 39755714 39755714 single base substitution C G intron_variant LIRI-JP 4 39756696 39756696 single base substitution G A intron_variant LIRI-JP 4 39756713 39756713 single base substitution A T intron_variant LIRI-JP 4 39758807 39758807 single base substitution A T intron_variant LIRI-JP 4 39759338 39759338 single base substitution G T intron_variant LIRI-JP 4 39762387 39762387 single base substitution G A intron_variant LIRI-JP 4 39765343 39765343 single base substitution A G intron_variant LIRI-JP 4 39765354 39765354 deletion of <=200bp T - intron_variant LIRI-JP 4 39767524 39767524 single base substitution T C intron_variant LIRI-JP 4 39768281 39768281 single base substitution T G intron_variant LIRI-JP 4 39768287 39768287 single base substitution T G intron_variant LIRI-JP 4 39768749 39768749 single base substitution A G intron_variant LIRI-JP 4 39769313 39769313 single base substitution G T intron_variant LIRI-JP 4 39769512 39769512 single base substitution G C intron_variant LIRI-JP 4 39770722 39770722 single base substitution G C intron_variant LIRI-JP 4 39770949 39770949 single base substitution A T intron_variant LIRI-JP 4 39771180 39771180 single base substitution A T intron_variant LIRI-JP 4 39773902 39773902 single base substitution A G intron_variant LIRI-JP 4 39777525 39777525 single base substitution A G intron_variant LIRI-JP 4 39780811 39780811 single base substitution A G 3_prime_UTR_variant LIRI-JP 4 39780811 39780811 single base substitution A G downstream_gene_variant LIRI-JP 4 39780811 39780811 single base substitution A G exon_variant LIRI-JP 4 39784891 39784891 single base substitution A G downstream_gene_variant LIRI-JP 4 39786013 39786013 single base substitution T A downstream_gene_variant LIRI-JP 4 39786641 39786642 deletion of <=200bp AG - downstream_gene_variant LUSC-KR 4 39695681 39695681 single base substitution G T upstream_gene_variant LUSC-KR 4 39699687 39699687 single base substitution A T 5_prime_UTR_premature_start_codon_gain_variant LUSC-KR 4 39699687 39699687 single base substitution A T upstream_gene_variant LUSC-KR 4 39703858 39703858 single base substitution T C intron_variant LUSC-KR 4 39703877 39703877 single base substitution T C intron_variant LUSC-KR 4 39705331 39705331 single base substitution G T intron_variant LUSC-KR 4 39705698 39705698 single base substitution C A intron_variant LUSC-KR 4 39707531 39707531 single base substitution G T intron_variant LUSC-KR 4 39707533 39707533 single base substitution G C intron_variant LUSC-KR 4 39715860 39715860 single base substitution C A intron_variant LUSC-KR 4 39723291 39723291 single base substitution T C intron_variant LUSC-KR 4 39724434 39724434 single base substitution G T intron_variant LUSC-KR 4 39724884 39724884 single base substitution T C intron_variant LUSC-KR 4 39724885 39724885 single base substitution C A intron_variant LUSC-KR 4 39741417 39741417 single base substitution G A intron_variant LUSC-KR 4 39742102 39742102 single base substitution T G intron_variant LUSC-KR 4 39745404 39745404 single base substitution A G intron_variant LUSC-KR 4 39746411 39746411 single base substitution C T intron_variant LUSC-KR 4 39747536 39747536 single base substitution A G intron_variant LUSC-KR 4 39758952 39758952 single base substitution A G intron_variant LUSC-KR 4 39768233 39768233 single base substitution G A intron_variant LUSC-KR 4 39773791 39773791 single base substitution A G intron_variant LUSC-KR 4 39782282 39782282 single base substitution C T 3_prime_UTR_variant LUSC-KR 4 39782282 39782282 single base substitution C T downstream_gene_variant MALY-DE 4 39698150 39698150 insertion of <=200bp - T upstream_gene_variant MALY-DE 4 39699825 39699825 single base substitution C G 5_prime_UTR_variant MALY-DE 4 39699825 39699825 single base substitution C G exon_variant MALY-DE 4 39699825 39699825 single base substitution C G upstream_gene_variant MALY-DE 4 39700764 39700764 single base substitution C G intron_variant MALY-DE 4 39700995 39700995 single base substitution C G intron_variant MALY-DE 4 39710562 39710562 single base substitution T A intron_variant MALY-DE 4 39712718 39712718 single base substitution T A intron_variant MALY-DE 4 39724893 39724893 single base substitution G A intron_variant MALY-DE 4 39726926 39726926 insertion of <=200bp - GGA intron_variant MALY-DE 4 39736656 39736656 single base substitution T G intron_variant MALY-DE 4 39745034 39745034 single base substitution T C intron_variant MALY-DE 4 39746537 39746537 single base substitution A T intron_variant MALY-DE 4 39748874 39748874 single base substitution C T intron_variant MALY-DE 4 39748879 39748879 single base substitution T G intron_variant MALY-DE 4 39748880 39748880 single base substitution A T intron_variant MALY-DE 4 39758398 39758398 single base substitution C A intron_variant MALY-DE 4 39775214 39775214 single base substitution G T intron_variant MALY-DE 4 39778752 39778756 deletion of <=200bp TACTC - intron_variant MALY-DE 4 39779750 39779750 single base substitution T A intron_variant MALY-DE 4 39782502 39782502 single base substitution A C 3_prime_UTR_variant MALY-DE 4 39782502 39782502 single base substitution A C downstream_gene_variant MALY-DE 4 39782632 39782632 single base substitution G A 3_prime_UTR_variant MALY-DE 4 39782632 39782632 single base substitution G A downstream_gene_variant MALY-DE 4 39783935 39783935 single base substitution A G 3_prime_UTR_variant MALY-DE 4 39783935 39783935 single base substitution A G downstream_gene_variant MALY-DE 4 39785129 39785129 single base substitution A G downstream_gene_variant MALY-DE 4 39788349 39788349 single base substitution A C downstream_gene_variant MELA-AU 4 39694691 39694691 single base substitution C T upstream_gene_variant MELA-AU 4 39695082 39695082 single base substitution G A upstream_gene_variant MELA-AU 4 39695438 39695438 single base substitution G A upstream_gene_variant MELA-AU 4 39695795 39695795 single base substitution G A upstream_gene_variant MELA-AU 4 39695801 39695801 single base substitution C T upstream_gene_variant MELA-AU 4 39695975 39695975 single base substitution G A upstream_gene_variant MELA-AU 4 39696674 39696674 single base substitution G A upstream_gene_variant MELA-AU 4 39696803 39696804 multiple base substitution (>=2bp and <=200bp) GG AA upstream_gene_variant MELA-AU 4 39697152 39697152 single base substitution G A upstream_gene_variant MELA-AU 4 39697189 39697189 single base substitution G A upstream_gene_variant MELA-AU 4 39697329 39697329 single base substitution G A upstream_gene_variant MELA-AU 4 39697486 39697486 single base substitution G A upstream_gene_variant MELA-AU 4 39698467 39698467 single base substitution C A upstream_gene_variant MELA-AU 4 39698489 39698489 single base substitution T C upstream_gene_variant MELA-AU 4 39698565 39698565 single base substitution C T upstream_gene_variant MELA-AU 4 39698855 39698855 insertion of <=200bp - C upstream_gene_variant MELA-AU 4 39699400 39699400 single base substitution G A upstream_gene_variant MELA-AU 4 39699753 39699753 single base substitution G A 5_prime_UTR_variant MELA-AU 4 39699753 39699753 single base substitution G A upstream_gene_variant MELA-AU 4 39699778 39699778 single base substitution G A 5_prime_UTR_variant MELA-AU 4 39699778 39699778 single base substitution G A exon_variant MELA-AU 4 39699778 39699778 single base substitution G A upstream_gene_variant MELA-AU 4 39699877 39699877 single base substitution G A 5_prime_UTR_variant MELA-AU 4 39699877 39699877 single base substitution G A exon_variant MELA-AU 4 39699877 39699877 single base substitution G A upstream_gene_variant MELA-AU 4 39699912 39699912 single base substitution G A 5_prime_UTR_variant MELA-AU 4 39699912 39699912 single base substitution G A exon_variant MELA-AU 4 39699912 39699912 single base substitution G A upstream_gene_variant MELA-AU 4 39701013 39701013 single base substitution C T intron_variant MELA-AU 4 39702097 39702097 single base substitution G A intron_variant MELA-AU 4 39703562 39703562 single base substitution G A intron_variant MELA-AU 4 39703960 39703960 single base substitution C T intron_variant MELA-AU 4 39704070 39704070 single base substitution C T intron_variant MELA-AU 4 39705349 39705350 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 4 39706033 39706033 single base substitution T A intron_variant MELA-AU 4 39706711 39706711 insertion of <=200bp - T intron_variant MELA-AU 4 39708029 39708029 single base substitution C T intron_variant MELA-AU 4 39708300 39708300 single base substitution A G intron_variant MELA-AU 4 39710024 39710024 single base substitution C T intron_variant MELA-AU 4 39710723 39710723 single base substitution C T intron_variant MELA-AU 4 39711666 39711666 single base substitution A C intron_variant MELA-AU 4 39711691 39711691 single base substitution A T intron_variant MELA-AU 4 39712019 39712019 single base substitution C T intron_variant MELA-AU 4 39712075 39712075 single base substitution T G intron_variant MELA-AU 4 39712079 39712079 single base substitution G A intron_variant MELA-AU 4 39712167 39712167 single base substitution G A intron_variant MELA-AU 4 39712395 39712395 single base substitution C T intron_variant MELA-AU 4 39713175 39713175 single base substitution C T intron_variant MELA-AU 4 39713620 39713620 single base substitution C T intron_variant MELA-AU 4 39714656 39714656 single base substitution C T intron_variant MELA-AU 4 39714799 39714799 single base substitution A T intron_variant MELA-AU 4 39715823 39715823 single base substitution T A intron_variant MELA-AU 4 39716379 39716379 single base substitution C T intron_variant MELA-AU 4 39716988 39716988 single base substitution C T intron_variant MELA-AU 4 39717086 39717086 single base substitution C T intron_variant MELA-AU 4 39717275 39717275 single base substitution T G intron_variant MELA-AU 4 39717475 39717475 single base substitution A G intron_variant MELA-AU 4 39717593 39717593 single base substitution C A intron_variant MELA-AU 4 39717817 39717817 single base substitution C T intron_variant MELA-AU 4 39718462 39718462 single base substitution C A intron_variant MELA-AU 4 39720264 39720264 single base substitution C T intron_variant MELA-AU 4 39720542 39720542 single base substitution G A intron_variant MELA-AU 4 39720627 39720627 single base substitution C G intron_variant MELA-AU 4 39721055 39721055 single base substitution C T intron_variant MELA-AU 4 39722101 39722101 single base substitution C T intron_variant MELA-AU 4 39722176 39722176 single base substitution T C intron_variant MELA-AU 4 39723153 39723153 single base substitution T C intron_variant MELA-AU 4 39723702 39723702 single base substitution C T intron_variant MELA-AU 4 39724060 39724060 single base substitution G T intron_variant MELA-AU 4 39724770 39724770 single base substitution C T intron_variant MELA-AU 4 39724904 39724904 single base substitution C T intron_variant MELA-AU 4 39725426 39725426 single base substitution C T intron_variant MELA-AU 4 39726251 39726251 single base substitution G A intron_variant MELA-AU 4 39726586 39726586 single base substitution C T intron_variant MELA-AU 4 39727368 39727368 single base substitution C T intron_variant MELA-AU 4 39727509 39727509 single base substitution C T intron_variant MELA-AU 4 39727905 39727905 single base substitution C T intron_variant MELA-AU 4 39728608 39728608 single base substitution C T intron_variant MELA-AU 4 39730282 39730282 single base substitution G A intron_variant MELA-AU 4 39730292 39730292 single base substitution C T intron_variant MELA-AU 4 39730297 39730297 single base substitution C T intron_variant MELA-AU 4 39730378 39730378 single base substitution C T intron_variant MELA-AU 4 39731017 39731017 single base substitution C T intron_variant MELA-AU 4 39731048 39731048 single base substitution C T intron_variant MELA-AU 4 39731213 39731213 single base substitution T C intron_variant MELA-AU 4 39731260 39731260 single base substitution C T intron_variant MELA-AU 4 39731322 39731322 single base substitution C T intron_variant MELA-AU 4 39731718 39731718 single base substitution T A intron_variant MELA-AU 4 39731886 39731886 single base substitution C T intron_variant MELA-AU 4 39732215 39732215 single base substitution C T intron_variant MELA-AU 4 39732716 39732716 single base substitution C A intron_variant MELA-AU 4 39733251 39733252 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 4 39735283 39735284 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 4 39735445 39735445 single base substitution C T intron_variant MELA-AU 4 39735828 39735828 single base substitution C G intron_variant MELA-AU 4 39736147 39736147 single base substitution G A intron_variant MELA-AU 4 39736882 39736882 single base substitution T C intron_variant MELA-AU 4 39736989 39736989 single base substitution C T intron_variant MELA-AU 4 39737091 39737091 single base substitution C T intron_variant MELA-AU 4 39737160 39737160 single base substitution C T intron_variant MELA-AU 4 39740835 39740835 single base substitution T C intron_variant MELA-AU 4 39741155 39741155 single base substitution C T intron_variant MELA-AU 4 39742265 39742265 single base substitution G A intron_variant MELA-AU 4 39742278 39742278 single base substitution C T intron_variant MELA-AU 4 39742703 39742703 single base substitution C T intron_variant MELA-AU 4 39744045 39744045 single base substitution C T intron_variant MELA-AU 4 39744136 39744136 single base substitution T G intron_variant MELA-AU 4 39744878 39744878 single base substitution A T intron_variant MELA-AU 4 39745084 39745084 single base substitution C A intron_variant MELA-AU 4 39745443 39745443 single base substitution C T intron_variant MELA-AU 4 39745479 39745479 single base substitution T G intron_variant MELA-AU 4 39745581 39745581 single base substitution C T intron_variant MELA-AU 4 39745947 39745947 single base substitution C T intron_variant MELA-AU 4 39747942 39747942 single base substitution G A intron_variant MELA-AU 4 39748200 39748200 single base substitution C T intron_variant MELA-AU 4 39748264 39748264 single base substitution C T intron_variant MELA-AU 4 39748972 39748972 single base substitution C T intron_variant MELA-AU 4 39751323 39751323 single base substitution G A intron_variant MELA-AU 4 39751733 39751733 single base substitution G A intron_variant MELA-AU 4 39752027 39752027 single base substitution C T intron_variant MELA-AU 4 39752263 39752263 single base substitution C T intron_variant MELA-AU 4 39752515 39752515 single base substitution C T intron_variant MELA-AU 4 39753191 39753191 single base substitution C T intron_variant MELA-AU 4 39753470 39753470 single base substitution C T intron_variant MELA-AU 4 39753999 39753999 single base substitution C T intron_variant MELA-AU 4 39754226 39754226 single base substitution G A intron_variant MELA-AU 4 39754281 39754294 deletion of <=200bp TGAATTCCTTGAGT - intron_variant MELA-AU 4 39755636 39755636 single base substitution G A intron_variant MELA-AU 4 39757169 39757169 single base substitution G A intron_variant MELA-AU 4 39758008 39758008 single base substitution C T intron_variant MELA-AU 4 39758614 39758614 single base substitution T C intron_variant MELA-AU 4 39758800 39758800 single base substitution C T intron_variant MELA-AU 4 39758935 39758935 single base substitution C T intron_variant MELA-AU 4 39759193 39759193 single base substitution C T intron_variant MELA-AU 4 39759435 39759435 single base substitution C T intron_variant MELA-AU 4 39759622 39759622 single base substitution C T intron_variant MELA-AU 4 39760444 39760444 single base substitution G T intron_variant MELA-AU 4 39761915 39761915 single base substitution C T intron_variant MELA-AU 4 39762648 39762648 single base substitution C T intron_variant MELA-AU 4 39762649 39762649 single base substitution C T intron_variant MELA-AU 4 39762998 39762998 single base substitution T A intron_variant MELA-AU 4 39763047 39763047 single base substitution T G intron_variant MELA-AU 4 39763105 39763105 single base substitution T G intron_variant MELA-AU 4 39763170 39763170 single base substitution C T intron_variant MELA-AU 4 39763267 39763267 single base substitution G A intron_variant MELA-AU 4 39763543 39763543 single base substitution C T intron_variant MELA-AU 4 39763656 39763656 single base substitution G A intron_variant MELA-AU 4 39764010 39764010 single base substitution G C intron_variant MELA-AU 4 39764473 39764473 single base substitution C T intron_variant MELA-AU 4 39764542 39764542 single base substitution C T intron_variant MELA-AU 4 39764804 39764804 single base substitution C T intron_variant MELA-AU 4 39766012 39766012 single base substitution C T intron_variant MELA-AU 4 39766068 39766068 single base substitution T A intron_variant MELA-AU 4 39766597 39766597 single base substitution C T intron_variant MELA-AU 4 39767188 39767188 single base substitution C T intron_variant MELA-AU 4 39767221 39767221 single base substitution C T intron_variant MELA-AU 4 39767303 39767303 single base substitution C T intron_variant MELA-AU 4 39767566 39767566 single base substitution C T intron_variant MELA-AU 4 39767572 39767572 single base substitution T C intron_variant MELA-AU 4 39767842 39767842 single base substitution C T intron_variant MELA-AU 4 39767990 39767990 single base substitution C T intron_variant MELA-AU 4 39768148 39768148 single base substitution T C intron_variant MELA-AU 4 39769123 39769123 single base substitution T C intron_variant MELA-AU 4 39769841 39769841 single base substitution C T intron_variant MELA-AU 4 39770035 39770035 single base substitution C T intron_variant MELA-AU 4 39770328 39770328 single base substitution C T intron_variant MELA-AU 4 39770600 39770600 single base substitution C T intron_variant MELA-AU 4 39770666 39770666 single base substitution G A intron_variant MELA-AU 4 39770803 39770804 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 4 39770923 39770923 single base substitution C T intron_variant MELA-AU 4 39771067 39771068 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 4 39771221 39771221 single base substitution C T intron_variant MELA-AU 4 39771234 39771234 single base substitution C T intron_variant MELA-AU 4 39771287 39771287 single base substitution C T intron_variant MELA-AU 4 39771467 39771467 single base substitution C T intron_variant MELA-AU 4 39771525 39771525 single base substitution A G intron_variant MELA-AU 4 39771556 39771556 single base substitution C T intron_variant MELA-AU 4 39771632 39771632 single base substitution C T intron_variant MELA-AU 4 39771646 39771647 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 4 39771655 39771655 single base substitution C T intron_variant MELA-AU 4 39771778 39771778 single base substitution T C intron_variant MELA-AU 4 39771784 39771784 single base substitution G A intron_variant MELA-AU 4 39771899 39771899 single base substitution C T intron_variant MELA-AU 4 39772147 39772147 single base substitution C T intron_variant MELA-AU 4 39772330 39772331 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 4 39772371 39772371 single base substitution C T intron_variant MELA-AU 4 39772376 39772376 single base substitution C T intron_variant MELA-AU 4 39772890 39772890 single base substitution C T intron_variant MELA-AU 4 39773572 39773572 single base substitution C T intron_variant MELA-AU 4 39773683 39773683 single base substitution C T intron_variant MELA-AU 4 39773904 39773904 single base substitution T G intron_variant MELA-AU 4 39774666 39774666 insertion of <=200bp - T intron_variant MELA-AU 4 39775574 39775574 single base substitution C A intron_variant MELA-AU 4 39775894 39775895 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 4 39776226 39776226 single base substitution C T intron_variant MELA-AU 4 39776648 39776648 single base substitution G A intron_variant MELA-AU 4 39777833 39777833 single base substitution G A intron_variant MELA-AU 4 39778550 39778550 single base substitution C T intron_variant MELA-AU 4 39778585 39778585 single base substitution C T intron_variant MELA-AU 4 39779867 39779867 single base substitution C T intron_variant MELA-AU 4 39779898 39779898 single base substitution C T intron_variant MELA-AU 4 39780296 39780296 single base substitution C T 3_prime_UTR_variant MELA-AU 4 39780296 39780296 single base substitution C T downstream_gene_variant MELA-AU 4 39780296 39780296 single base substitution C T exon_variant MELA-AU 4 39780766 39780766 single base substitution C T 3_prime_UTR_variant MELA-AU 4 39780766 39780766 single base substitution C T downstream_gene_variant MELA-AU 4 39780766 39780766 single base substitution C T exon_variant MELA-AU 4 39780902 39780902 single base substitution C T 3_prime_UTR_variant MELA-AU 4 39780902 39780902 single base substitution C T downstream_gene_variant MELA-AU 4 39780902 39780902 single base substitution C T exon_variant MELA-AU 4 39781480 39781480 single base substitution T A 3_prime_UTR_variant MELA-AU 4 39781480 39781480 single base substitution T A downstream_gene_variant MELA-AU 4 39781480 39781480 single base substitution T A exon_variant MELA-AU 4 39781996 39781996 single base substitution C G 3_prime_UTR_variant MELA-AU 4 39781996 39781996 single base substitution C G downstream_gene_variant MELA-AU 4 39784830 39784830 single base substitution C T downstream_gene_variant MELA-AU 4 39785684 39785684 single base substitution C T downstream_gene_variant MELA-AU 4 39785791 39785791 single base substitution A G downstream_gene_variant MELA-AU 4 39785861 39785862 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 4 39786096 39786096 single base substitution G C downstream_gene_variant MELA-AU 4 39786469 39786469 single base substitution C T downstream_gene_variant MELA-AU 4 39787540 39787540 single base substitution C T downstream_gene_variant MELA-AU 4 39788202 39788202 single base substitution C T downstream_gene_variant MELA-AU 4 39788423 39788423 single base substitution A G downstream_gene_variant MELA-AU 4 39788440 39788440 single base substitution C T downstream_gene_variant MELA-AU 4 39788453 39788453 single base substitution C T downstream_gene_variant MELA-AU 4 39788918 39788918 single base substitution C T downstream_gene_variant MELA-AU 4 39789091 39789091 single base substitution C A downstream_gene_variant ORCA-IN 4 39699091 39699091 single base substitution T A upstream_gene_variant OV-AU 4 39697153 39697153 single base substitution A T upstream_gene_variant OV-AU 4 39698360 39698360 single base substitution T C upstream_gene_variant OV-AU 4 39702760 39702760 single base substitution T A intron_variant OV-AU 4 39704735 39704735 single base substitution C T intron_variant OV-AU 4 39714398 39714398 single base substitution T C intron_variant OV-AU 4 39718882 39718882 single base substitution C G intron_variant OV-AU 4 39726078 39726078 single base substitution G C intron_variant OV-AU 4 39731148 39731148 single base substitution C T intron_variant OV-AU 4 39733780 39733780 single base substitution T C intron_variant OV-AU 4 39734630 39734630 single base substitution T C intron_variant OV-AU 4 39738499 39738499 single base substitution G A intron_variant OV-AU 4 39742253 39742253 single base substitution C T intron_variant OV-AU 4 39743944 39743944 single base substitution C G intron_variant OV-AU 4 39745359 39745359 single base substitution A G intron_variant OV-AU 4 39746705 39746705 single base substitution T C intron_variant OV-AU 4 39748182 39748182 single base substitution C G intron_variant OV-AU 4 39750999 39750999 single base substitution G C intron_variant OV-AU 4 39760119 39760119 single base substitution G A intron_variant OV-AU 4 39765091 39765091 single base substitution G A intron_variant OV-AU 4 39768527 39768527 single base substitution A G intron_variant OV-AU 4 39771469 39771469 single base substitution C T intron_variant OV-US 4 39747381 39747385 deletion of <=200bp ACCAA - exon_variant OV-US 4 39747381 39747385 deletion of <=200bp ACCAA - frameshift_variant YQ56 OV-US 4 39747381 39747385 deletion of <=200bp ACCAA - intron_variant PACA-AU 4 39694787 39694787 single base substitution T G upstream_gene_variant PACA-AU 4 39695202 39695202 single base substitution C T upstream_gene_variant PACA-AU 4 39697323 39697323 single base substitution G T upstream_gene_variant PACA-AU 4 39697598 39697602 deletion of <=200bp TAATC - upstream_gene_variant PACA-AU 4 39699305 39699305 single base substitution C T upstream_gene_variant PACA-AU 4 39701306 39701306 single base substitution T G intron_variant PACA-AU 4 39703792 39703792 insertion of <=200bp - TTGGTT intron_variant PACA-AU 4 39708676 39708676 single base substitution G A intron_variant PACA-AU 4 39709503 39709503 single base substitution G T intron_variant PACA-AU 4 39709504 39709504 single base substitution G T intron_variant PACA-AU 4 39710490 39710490 single base substitution A G intron_variant PACA-AU 4 39713059 39713059 single base substitution G A intron_variant PACA-AU 4 39714525 39714525 single base substitution G A intron_variant PACA-AU 4 39718840 39718840 single base substitution C T intron_variant PACA-AU 4 39724561 39724561 single base substitution G A intron_variant PACA-AU 4 39727734 39727734 deletion of <=200bp T - intron_variant PACA-AU 4 39732964 39732964 single base substitution A G intron_variant PACA-AU 4 39738083 39738083 deletion of <=200bp A - intron_variant PACA-AU 4 39746278 39746278 single base substitution G A intron_variant PACA-AU 4 39747074 39747074 single base substitution A G intron_variant PACA-AU 4 39759442 39759442 single base substitution C T intron_variant PACA-AU 4 39761228 39761228 single base substitution A G intron_variant PACA-AU 4 39767777 39767777 single base substitution G T intron_variant PACA-AU 4 39768200 39768200 single base substitution G T intron_variant PACA-AU 4 39769776 39769776 single base substitution C T intron_variant PACA-AU 4 39773168 39773168 single base substitution G T intron_variant PACA-AU 4 39777541 39777541 single base substitution G A intron_variant PACA-AU 4 39781519 39781519 single base substitution G A 3_prime_UTR_variant PACA-AU 4 39781519 39781519 single base substitution G A downstream_gene_variant PACA-AU 4 39781519 39781519 single base substitution G A exon_variant PACA-CA 4 39694964 39694964 insertion of <=200bp - T upstream_gene_variant PACA-CA 4 39695012 39695012 single base substitution G A upstream_gene_variant PACA-CA 4 39703443 39703443 single base substitution C T intron_variant PACA-CA 4 39705176 39705176 single base substitution A G intron_variant PACA-CA 4 39705187 39705187 single base substitution A G intron_variant PACA-CA 4 39710312 39710312 single base substitution G A intron_variant PACA-CA 4 39713379 39713379 single base substitution C T intron_variant PACA-CA 4 39717590 39717590 single base substitution T C intron_variant PACA-CA 4 39722097 39722097 single base substitution T C intron_variant PACA-CA 4 39722242 39722242 single base substitution C T intron_variant PACA-CA 4 39723712 39723712 deletion of <=200bp A - intron_variant PACA-CA 4 39725599 39725599 insertion of <=200bp - T intron_variant PACA-CA 4 39727572 39727572 single base substitution A T intron_variant PACA-CA 4 39728991 39728991 single base substitution G A intron_variant PACA-CA 4 39733592 39733592 single base substitution T C intron_variant PACA-CA 4 39735495 39735495 single base substitution C T intron_variant PACA-CA 4 39740090 39740090 single base substitution G T intron_variant PACA-CA 4 39741140 39741140 single base substitution C A intron_variant PACA-CA 4 39741772 39741772 single base substitution T G intron_variant PACA-CA 4 39746165 39746165 single base substitution C T intron_variant PACA-CA 4 39746444 39746444 single base substitution G A intron_variant PACA-CA 4 39754504 39754504 single base substitution C T intron_variant PACA-CA 4 39754641 39754641 insertion of <=200bp - A intron_variant PACA-CA 4 39755574 39755574 single base substitution T C intron_variant PACA-CA 4 39755658 39755658 single base substitution G A intron_variant PACA-CA 4 39756442 39756442 single base substitution A G intron_variant PACA-CA 4 39756993 39756993 single base substitution C T intron_variant PACA-CA 4 39762242 39762242 single base substitution G T intron_variant PACA-CA 4 39767558 39767558 single base substitution T C intron_variant PACA-CA 4 39771016 39771016 deletion of <=200bp C - intron_variant PACA-CA 4 39772902 39772902 single base substitution G A intron_variant PACA-CA 4 39773190 39773190 deletion of <=200bp G - intron_variant PACA-CA 4 39778602 39778602 single base substitution G C intron_variant PACA-CA 4 39779378 39779378 single base substitution G C 3_prime_UTR_variant PACA-CA 4 39779378 39779378 single base substitution G C exon_variant PACA-CA 4 39779378 39779378 single base substitution G C intron_variant PACA-CA 4 39779378 39779378 single base substitution G C missense_variant S108T 323G>C PACA-CA 4 39779378 39779378 single base substitution G C missense_variant S159T 476G>C PACA-CA 4 39779378 39779378 single base substitution G C missense_variant S98T 293G>C PACA-CA 4 39780062 39780062 deletion of <=200bp A - 3_prime_UTR_variant PACA-CA 4 39780062 39780062 deletion of <=200bp A - downstream_gene_variant PACA-CA 4 39780062 39780062 deletion of <=200bp A - exon_variant PACA-CA 4 39780651 39780651 insertion of <=200bp - T 3_prime_UTR_variant PACA-CA 4 39780651 39780651 insertion of <=200bp - T downstream_gene_variant PACA-CA 4 39780651 39780651 insertion of <=200bp - T exon_variant PACA-CA 4 39781592 39781592 single base substitution G A 3_prime_UTR_variant PACA-CA 4 39781592 39781592 single base substitution G A downstream_gene_variant PACA-CA 4 39781592 39781592 single base substitution G A exon_variant PACA-CA 4 39783235 39783235 single base substitution T G 3_prime_UTR_variant PACA-CA 4 39783235 39783235 single base substitution T G downstream_gene_variant PACA-CA 4 39783815 39783815 single base substitution A G 3_prime_UTR_variant PACA-CA 4 39783815 39783815 single base substitution A G downstream_gene_variant PACA-CA 4 39788268 39788268 deletion of <=200bp C - downstream_gene_variant PAEN-AU 4 39714713 39714713 single base substitution A C intron_variant PAEN-AU 4 39714804 39714804 single base substitution C G intron_variant PAEN-AU 4 39726659 39726659 single base substitution C A intron_variant PAEN-AU 4 39761815 39761815 single base substitution G C intron_variant PAEN-AU 4 39787152 39787152 single base substitution C A downstream_gene_variant PBCA-DE 4 39697346 39697346 single base substitution G T upstream_gene_variant PBCA-DE 4 39705110 39705110 single base substitution G C intron_variant PBCA-DE 4 39709063 39709063 single base substitution G A intron_variant PBCA-DE 4 39715512 39715513 deletion of <=200bp TT - intron_variant PBCA-DE 4 39716051 39716051 deletion of <=200bp A - intron_variant PBCA-DE 4 39728797 39728797 single base substitution T G intron_variant PBCA-DE 4 39729152 39729152 single base substitution T A intron_variant PBCA-DE 4 39754234 39754234 single base substitution G T intron_variant PBCA-DE 4 39754969 39754969 single base substitution G T intron_variant PBCA-DE 4 39759704 39759704 single base substitution T A intron_variant PBCA-DE 4 39763805 39763807 deletion of <=200bp AAT - intron_variant PBCA-DE 4 39764278 39764278 single base substitution A G intron_variant PBCA-DE 4 39766807 39766807 single base substitution C T intron_variant PBCA-DE 4 39772823 39772823 single base substitution G A intron_variant PBCA-DE 4 39785150 39785150 single base substitution C T downstream_gene_variant PRAD-CA 4 39750791 39750791 single base substitution A G intron_variant PRAD-CA 4 39766579 39766579 single base substitution T G intron_variant PRAD-CA 4 39768931 39768931 single base substitution G T intron_variant PRAD-CA 4 39787414 39787414 single base substitution C T downstream_gene_variant PRAD-UK 4 39698450 39698450 single base substitution A C upstream_gene_variant PRAD-UK 4 39703120 39703120 insertion of <=200bp - ATAGAG intron_variant PRAD-UK 4 39739613 39739613 single base substitution A C intron_variant PRAD-UK 4 39749337 39749337 single base substitution C T intron_variant PRAD-UK 4 39753205 39753205 single base substitution A G intron_variant PRAD-UK 4 39753802 39753802 single base substitution G T intron_variant PRAD-UK 4 39766847 39766847 single base substitution T G intron_variant PRAD-UK 4 39782396 39782396 deletion of <=200bp A - 3_prime_UTR_variant PRAD-UK 4 39782396 39782396 deletion of <=200bp A - downstream_gene_variant PRAD-UK 4 39783153 39783153 single base substitution G A 3_prime_UTR_variant PRAD-UK 4 39783153 39783153 single base substitution G A downstream_gene_variant PRAD-UK 4 39783809 39783809 single base substitution T C 3_prime_UTR_variant PRAD-UK 4 39783809 39783809 single base substitution T C downstream_gene_variant READ-US 4 39757308 39757308 single base substitution A G exon_variant READ-US 4 39757308 39757308 single base substitution A G intron_variant READ-US 4 39757308 39757308 single base substitution A G missense_variant N32S 95A>G READ-US 4 39757308 39757308 single base substitution A G missense_variant N83S 248A>G READ-US 4 39757335 39757335 single base substitution G A exon_variant READ-US 4 39757335 39757335 single base substitution G A intron_variant READ-US 4 39757335 39757335 single base substitution G A missense_variant C41Y 122G>A READ-US 4 39757335 39757335 single base substitution G A missense_variant C92Y 275G>A RECA-EU 4 39709058 39709058 single base substitution G T intron_variant RECA-EU 4 39727996 39727996 single base substitution C A intron_variant RECA-EU 4 39729368 39729368 single base substitution A T intron_variant RECA-EU 4 39730474 39730474 single base substitution A T intron_variant RECA-EU 4 39735136 39735136 single base substitution A G intron_variant RECA-EU 4 39748420 39748420 single base substitution A T intron_variant RECA-EU 4 39757793 39757793 single base substitution G T intron_variant RECA-EU 4 39773466 39773466 single base substitution G A intron_variant RECA-EU 4 39779112 39779112 single base substitution T C intron_variant SKCA-BR 4 39694768 39694781 deletion of <=200bp AATAATTTTATTTT - upstream_gene_variant SKCA-BR 4 39699091 39699099 deletion of <=200bp TGAGAGAGA - upstream_gene_variant SKCA-BR 4 39699606 39699606 single base substitution A C upstream_gene_variant SKCA-BR 4 39700334 39700334 single base substitution T G intron_variant SKCA-BR 4 39703380 39703380 insertion of <=200bp - GT intron_variant SKCA-BR 4 39703846 39703866 deletion of <=200bp CTTTTCTTTTTTTTTTTTTTT - intron_variant SKCA-BR 4 39709643 39709643 single base substitution A G intron_variant SKCA-BR 4 39712807 39712807 single base substitution G A intron_variant SKCA-BR 4 39715168 39715168 insertion of <=200bp - CT intron_variant SKCA-BR 4 39716167 39716170 deletion of <=200bp TATA - intron_variant SKCA-BR 4 39716975 39716975 single base substitution G A intron_variant SKCA-BR 4 39717230 39717230 single base substitution C T intron_variant SKCA-BR 4 39719342 39719342 single base substitution C T intron_variant SKCA-BR 4 39721172 39721172 single base substitution C T intron_variant SKCA-BR 4 39724037 39724038 deletion of <=200bp GT - intron_variant SKCA-BR 4 39724982 39724982 insertion of <=200bp - CT intron_variant SKCA-BR 4 39727014 39727014 single base substitution A C intron_variant SKCA-BR 4 39728205 39728205 single base substitution G A intron_variant SKCA-BR 4 39730447 39730447 insertion of <=200bp - GT intron_variant SKCA-BR 4 39730593 39730594 deletion of <=200bp CT - intron_variant SKCA-BR 4 39733756 39733756 single base substitution T A intron_variant SKCA-BR 4 39737566 39737566 single base substitution G C intron_variant SKCA-BR 4 39738586 39738596 deletion of <=200bp GTGAGAGTTTA - intron_variant SKCA-BR 4 39741008 39741008 single base substitution G A intron_variant SKCA-BR 4 39744185 39744185 single base substitution T C intron_variant SKCA-BR 4 39750240 39750242 deletion of <=200bp CAA - intron_variant SKCA-BR 4 39751121 39751131 deletion of <=200bp AAAAACTAAAC - intron_variant SKCA-BR 4 39756629 39756629 single base substitution A G intron_variant SKCA-BR 4 39758651 39758652 deletion of <=200bp TG - intron_variant SKCA-BR 4 39758865 39758865 single base substitution C T intron_variant SKCA-BR 4 39759321 39759321 single base substitution C T intron_variant SKCA-BR 4 39762340 39762341 deletion of <=200bp AC - intron_variant SKCA-BR 4 39767576 39767576 single base substitution C T intron_variant SKCA-BR 4 39768470 39768470 single base substitution C T intron_variant SKCA-BR 4 39768909 39768909 single base substitution C T intron_variant SKCA-BR 4 39772151 39772151 single base substitution G A intron_variant SKCA-BR 4 39772540 39772540 single base substitution A G intron_variant SKCA-BR 4 39776233 39776233 single base substitution A G intron_variant SKCA-BR 4 39778239 39778239 single base substitution G A intron_variant SKCA-BR 4 39779083 39779083 single base substitution T C intron_variant SKCA-BR 4 39780662 39780662 insertion of <=200bp - AC 3_prime_UTR_variant SKCA-BR 4 39780662 39780662 insertion of <=200bp - AC downstream_gene_variant SKCA-BR 4 39780662 39780662 insertion of <=200bp - AC exon_variant SKCA-BR 4 39783729 39783729 single base substitution C T 3_prime_UTR_variant SKCA-BR 4 39783729 39783729 single base substitution C T downstream_gene_variant SKCA-BR 4 39785962 39785962 single base substitution C T downstream_gene_variant SKCA-BR 4 39787846 39787847 deletion of <=200bp CT - downstream_gene_variant SKCM-US 4 39739052 39739052 single base substitution C T exon_variant SKCM-US 4 39739052 39739052 single base substitution C T intron_variant SKCM-US 4 39739052 39739052 single base substitution C T stop_gained Q26* 76C>T SKCM-US 4 39757304 39757304 single base substitution C T exon_variant SKCM-US 4 39757304 39757304 single base substitution C T intron_variant SKCM-US 4 39757304 39757304 single base substitution C T missense_variant P31S 91C>T SKCM-US 4 39757304 39757304 single base substitution C T missense_variant P82S 244C>T STAD-US 4 39779998 39779998 single base substitution T G 3_prime_UTR_variant STAD-US 4 39779998 39779998 single base substitution T G exon_variant STAD-US 4 39779998 39779998 single base substitution T G missense_variant L122V 364T>G STAD-US 4 39779998 39779998 single base substitution T G missense_variant L132V 394T>G STAD-US 4 39779998 39779998 single base substitution T G missense_variant L140V 418T>G STAD-US 4 39779998 39779998 single base substitution T G missense_variant L183V 547T>G THCA-SA 4 39783076 39783076 single base substitution A C 3_prime_UTR_variant THCA-SA 4 39783076 39783076 single base substitution A C downstream_gene_variant UCEC-US 4 39747420 39747420 single base substitution A C exon_variant UCEC-US 4 39747420 39747420 single base substitution A C intron_variant UCEC-US 4 39747420 39747420 single base substitution A C missense_variant N69T 206A>C UCEC-US 4 39776532 39776532 single base substitution G T 3_prime_UTR_variant UCEC-US 4 39776532 39776532 single base substitution G T exon_variant UCEC-US 4 39776532 39776532 single base substitution G T intron_variant UCEC-US 4 39776532 39776532 single base substitution G T missense_variant Q126H 378G>T UCEC-US 4 39776532 39776532 single base substitution G T missense_variant Q75H 225G>T UCEC-US 4 39779984 39779984 single base substitution C T 3_prime_UTR_variant UCEC-US 4 39779984 39779984 single base substitution C T exon_variant UCEC-US 4 39779984 39779984 single base substitution C T missense_variant A117V 350C>T UCEC-US 4 39779984 39779984 single base substitution C T missense_variant A127V 380C>T UCEC-US 4 39779984 39779984 single base substitution C T missense_variant A135V 404C>T UCEC-US 4 39779984 39779984 single base substitution C T missense_variant A178V 533C>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand 40M COSM5586947 c.319C>T p.R107C Substitution - Missense 4:39774853-39774853 + TCGA-CK-5916-01 COSM1429640 c.320G>A p.R107H Substitution - Missense 4:39774854-39774854 + ESO17T COSM1173054 c.164G>A p.R55K Substitution - Missense 4:39745758-39745758 + CSCC-60-T COSM4474019 c.188C>T p.P63L Substitution - Missense 4:39745782-39745782 + PD5959a COSM5768745 c.78A>G p.Q26Q Substitution - coding silent 4:39737434-39737434 + TCGA-B5-A0JY-01 COSM1055271 c.533C>T p.A178V Substitution - Missense 4:39778364-39778364 + TCGA-AA-A010-01 COSM286232 c.157+8C>A p.? Unknown 4:39737521-39737521 + 27 COSM5586947 c.319C>T p.R107C Substitution - Missense 4:39774853-39774853 + TCGA-24-1469-01 COSM69089 c.167_171delACCAA p.Y56fs*12 Deletion - Frameshift 4:39745761-39745765 + TCGA-AX-A05Z-01 COSM1055269 c.206A>C p.N69T Substitution - Missense 4:39745800-39745800 + T155 COSM1176651 c.529A>G p.N177D Substitution - Missense 4:39778360-39778360 + 66 COSM5188909 c.490delA p.I166fs*1 Deletion - Frameshift 4:39777772-39777772 + TCGA-AU-6004-01 COSM1429639 c.220C>T p.R74W Substitution - Missense 4:39755660-39755660 + ESO15T COSM1173055 c.583G>A p.E195K Substitution - Missense 4:39778414-39778414 + TCGA-GN-A26C-01 COSM3603594 c.76C>T p.Q26* Substitution - Nonsense 4:39737432-39737432 + TCGA-WS-AB45-01 COSM5188909 c.490delA p.I166fs*1 Deletion - Frameshift 4:39777772-39777772 + TCGA-HE-A5NF-01 COSM3993665 c.293A>G p.D98G Substitution - Missense 4:39755733-39755733 + T3118 COSM4738684 c.50T>C p.L17P Substitution - Missense 4:39698377-39698377 + TCGA-CM-6162-01 COSM5159098 c.369T>A p.D123E Substitution - Missense 4:39774903-39774903 + TCGA-CG-5721-01 COSM4124607 c.547T>G p.L183V Substitution - Missense 4:39778378-39778378 + TCGA-AP-A0LM-01 COSM1055270 c.378G>T p.Q126H Substitution - Missense 4:39774912-39774912 + TCGA-ED-A4XI-01 COSM4913269 c.558A>G p.K186K Substitution - coding silent 4:39778389-39778389 + TCGA-29-1776-01 COSM1328529 c.400-1G>C p.? Unknown 4:39777681-39777681 + TCGA-EI-6509-01 COSM3428493 c.275G>A p.C92Y Substitution - Missense 4:39755715-39755715 + ESO-721 COSM1269622 c.89A>T p.D30V Substitution - Missense 4:39737445-39737445 + TCGA-G4-6628-01 COSM1429641 c.458C>T p.A153V Substitution - Missense 4:39777740-39777740 + SNU-175 COSM2846772 c.321C>T p.R107R Substitution - coding silent 4:39774855-39774855 + TCGA-AF-6655-01 COSM1567342 c.248A>G p.N83S Substitution - Missense 4:39755688-39755688 + OV207 COSM252901 c.247A>G p.N83D Substitution - Missense 4:39755687-39755687 + TCGA-EE-A2MG-06 COSM3603595 c.244C>T p.P82S Substitution - Missense 4:39755684-39755684 + PCSI_0492_Pa_P_526 COSM4964808 c.476G>C p.S159T Substitution - Missense 4:39777758-39777758 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.50308 4p14 602846

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer ACCAA - Frameshift p.Y56Sfs*12 c.167_171delACCAA 4 39747381 OV A - Frameshift p.I166*fs*1 c.496delA 4 39779392 BLCA A T Missense p.D30V c.89A>T 4 39739065 ESCA C A 3-UTRSNV . c.600+80C>A 4 39780131 RCCC C T IntronicSNV . c.300-3510C>T 4 39772944 CM C T IntronicSNV . c.300-3739C>T 4 39772715 NSCLC C T IntronicSNV . c.300-3742C>T 4 39772712 CM C T IntronicSNV . c.63+7682C>T 4 39707692 CLL C T Missense p.P82S c.244C>T 4 39757304 CM C T Nonsense p.Q26* c.76C>T 4 39739052 CM G A 3-UTRSNV . c.600+2581G>A 4 39782632 DLBCL G A Missense p.D189N c.565G>A 4 39780016 LUAD T - IntronicDeletion . c.400-13delT 4 39779285 ESCA