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 17 73164440 73164440 + Silent SNP G G C TCGA-DK-A3X1-01A-12D-A22Z-08 TCGA-DK-A3X1-10A-01D-A22Z-08 g.chr17:73164440G>C c.153C>G c.(151-153)gtC>gtG p.V51V BLCA 17 73164461 73164461 + Missense_Mutation SNP G G C TCGA-DK-A2I4-01A-11D-A21A-08 TCGA-DK-A2I4-10A-01D-A21A-08 g.chr17:73164461G>C c.132C>G c.(130-132)ttC>ttG p.F44L BLCA 17 73177191 73177191 + Silent SNP T T C TCGA-XF-A9T8-01A-11D-A391-08 TCGA-XF-A9T8-10A-01D-A394-08 g.chr17:73177191T>C c.114A>G c.(112-114)acA>acG p.T38T BRCA 17 73177269 73177269 + Silent SNP A A T TCGA-AR-A2LE-01A-11D-A17W-09 TCGA-AR-A2LE-10A-01D-A17W-09 g.chr17:73177269A>T c.36T>A c.(34-36)acT>acA p.T12T DLBC 17 73177275 73177275 + Silent SNP G G A TCGA-FF-8043-01A-11D-2210-10 TCGA-FF-8043-10A-01D-2210-10 g.chr17:73177275G>A c.30C>T c.(28-30)gtC>gtT p.V10V GBMLGG 17 73177151 73177151 + Splice_Site SNP C C G TCGA-DU-7019-01A-11D-2024-08 TCGA-DU-7019-10A-01D-2024-08 g.chr17:73177151C>G c.e2+1 LAML 17 73170871 73170872 + Frame_Shift_Ins INS - - TA TCGA-AB-2927-03A-01W-0755-09 TCGA-AB-2927-11A-01W-0755-09 g.chr17:73170871_73170872insTA c.71_72insTA c.(70-72)atcfs p.I24fs LGG 17 73177151 73177151 + Splice_Site SNP C C G TCGA-DU-7019-01A-11D-2024-08 TCGA-DU-7019-10A-01D-2024-08 g.chr17:73177151C>G c.e2+1 LIHC 17 73177179 73177179 + Silent SNP T T C TCGA-G3-AAV7-01A-11D-A382-10 TCGA-G3-AAV7-10A-01D-A385-10 g.chr17:73177179T>C c.126A>G c.(124-126)aaA>aaG p.K42K LUAD 17 73177235 73177235 + Missense_Mutation SNP C C A TCGA-95-7043-01A-11D-1945-08 TCGA-95-7043-10A-01D-1946-08 g.chr17:73177235C>A c.70G>T c.(70-72)Ggg>Tgg p.G24W SKCM 17 73164461 73164461 + Silent SNP G G A TCGA-D3-A5GL-06A-11D-A27K-08 TCGA-D3-A5GL-10A-01D-A27N-08 g.chr17:73164461G>A c.132C>T c.(130-132)ttC>ttT p.F44F SKCM 17 73164463 73164463 + Missense_Mutation SNP A A G TCGA-EE-A3AB-06A-11D-A196-08 TCGA-EE-A3AB-10A-01D-A198-08 g.chr17:73164463A>G c.130T>C c.(130-132)Ttc>Ctc p.F44L SKCM 17 73170892 73170892 + Silent SNP G G A TCGA-FS-A1ZZ-06A-11D-A197-08 TCGA-FS-A1ZZ-10A-01D-A199-08 g.chr17:73170892G>A c.51C>T c.(49-51)ttC>ttT p.F17F

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 17 73164440 73164440 single base substitution G C synonymous_variant V51V 153C>G BLCA-US 17 73164440 73164440 single base substitution G C synonymous_variant V70V 210C>G BLCA-US 17 73164440 73164440 single base substitution G C synonymous_variant V94V 282C>G BLCA-US 17 73164461 73164461 single base substitution G C missense_variant F44L 132C>G BLCA-US 17 73164461 73164461 single base substitution G C missense_variant F63L 189C>G BLCA-US 17 73164461 73164461 single base substitution G C missense_variant F87L 261C>G BRCA-EU 17 73158523 73158523 single base substitution C G downstream_gene_variant BRCA-EU 17 73158862 73158862 single base substitution C G downstream_gene_variant BRCA-EU 17 73159776 73159776 single base substitution C T downstream_gene_variant BRCA-EU 17 73160415 73160415 single base substitution C A downstream_gene_variant BRCA-EU 17 73160416 73160416 single base substitution C G downstream_gene_variant BRCA-EU 17 73160905 73160905 single base substitution G C downstream_gene_variant BRCA-EU 17 73161847 73161847 single base substitution A G downstream_gene_variant BRCA-EU 17 73163380 73163380 single base substitution C G downstream_gene_variant BRCA-EU 17 73164444 73164444 single base substitution C G missense_variant G50A 149G>C BRCA-EU 17 73164444 73164444 single base substitution C G missense_variant G69A 206G>C BRCA-EU 17 73164444 73164444 single base substitution C G missense_variant G93A 278G>C BRCA-EU 17 73166467 73166467 single base substitution C T intron_variant BRCA-EU 17 73166932 73166932 single base substitution G A intron_variant BRCA-EU 17 73167166 73167166 single base substitution A T intron_variant BRCA-EU 17 73169574 73169574 single base substitution T G intron_variant BRCA-EU 17 73171814 73171814 single base substitution G T intron_variant BRCA-EU 17 73172174 73172174 single base substitution C T intron_variant BRCA-EU 17 73173204 73173204 single base substitution C A intron_variant BRCA-EU 17 73173463 73173463 single base substitution A C intron_variant BRCA-EU 17 73174386 73174386 single base substitution G A intron_variant BRCA-EU 17 73175337 73175337 single base substitution T C intron_variant BRCA-EU 17 73175751 73175751 single base substitution A G intron_variant BRCA-EU 17 73178178 73178178 single base substitution A C intron_variant BRCA-EU 17 73178780 73178780 single base substitution C T intron_variant BRCA-EU 17 73178780 73178780 single base substitution C T upstream_gene_variant BRCA-EU 17 73179944 73179944 single base substitution C A upstream_gene_variant BRCA-EU 17 73180101 73180101 single base substitution C G upstream_gene_variant BRCA-EU 17 73180363 73180363 single base substitution G A upstream_gene_variant BRCA-EU 17 73180615 73180615 single base substitution C G upstream_gene_variant BRCA-EU 17 73181224 73181224 single base substitution C T upstream_gene_variant BRCA-EU 17 73181338 73181339 deletion of <=200bp AC - upstream_gene_variant BRCA-EU 17 73181868 73181868 single base substitution A C upstream_gene_variant BRCA-EU 17 73182008 73182008 single base substitution G A upstream_gene_variant BRCA-EU 17 73182677 73182677 single base substitution G A upstream_gene_variant BRCA-EU 17 73183172 73183172 single base substitution T C upstream_gene_variant BRCA-EU 17 73183299 73183299 single base substitution C T upstream_gene_variant BRCA-EU 17 73184040 73184040 single base substitution A C upstream_gene_variant BRCA-FR 17 73159148 73159148 single base substitution G A downstream_gene_variant BRCA-FR 17 73164444 73164444 single base substitution C G missense_variant G50A 149G>C BRCA-FR 17 73164444 73164444 single base substitution C G missense_variant G69A 206G>C BRCA-FR 17 73164444 73164444 single base substitution C G missense_variant G93A 278G>C BRCA-FR 17 73173204 73173204 single base substitution C A intron_variant BRCA-FR 17 73178583 73178583 single base substitution C G 5_prime_UTR_variant BRCA-FR 17 73178583 73178583 single base substitution C G intron_variant BRCA-FR 17 73179944 73179944 single base substitution C A upstream_gene_variant BRCA-FR 17 73180101 73180101 single base substitution C G upstream_gene_variant BRCA-UK 17 73170867 73170867 single base substitution C T intron_variant BRCA-UK 17 73170867 73170867 single base substitution C T missense_variant E26K 76G>A BRCA-UK 17 73170867 73170867 single base substitution C T missense_variant E69K 205G>A BRCA-UK 17 73173558 73173558 single base substitution G A intron_variant BRCA-UK 17 73174510 73174510 single base substitution G A intron_variant BRCA-US 17 73177269 73177269 single base substitution A T 5_prime_UTR_variant BRCA-US 17 73177269 73177269 single base substitution A T synonymous_variant T12T 36T>A CLLE-ES 17 73164384 73164384 single base substitution T C 3_prime_UTR_variant CLLE-ES 17 73169573 73169573 single base substitution T G intron_variant ESAD-UK 17 73160814 73160814 single base substitution C A downstream_gene_variant ESAD-UK 17 73162935 73162935 single base substitution G A downstream_gene_variant ESAD-UK 17 73163577 73163577 single base substitution G A 3_prime_UTR_variant ESAD-UK 17 73163577 73163577 single base substitution G A downstream_gene_variant ESAD-UK 17 73164014 73164014 single base substitution T G 3_prime_UTR_variant ESAD-UK 17 73164014 73164014 single base substitution T G downstream_gene_variant ESAD-UK 17 73164065 73164065 single base substitution T G 3_prime_UTR_variant ESAD-UK 17 73164065 73164065 single base substitution T G downstream_gene_variant ESAD-UK 17 73165434 73165434 single base substitution G T intron_variant ESAD-UK 17 73165546 73165546 single base substitution T G intron_variant ESAD-UK 17 73167406 73167406 single base substitution G A intron_variant ESAD-UK 17 73170729 73170729 single base substitution C A intron_variant ESAD-UK 17 73172376 73172376 single base substitution G A intron_variant ESAD-UK 17 73174753 73174753 single base substitution T G intron_variant ESAD-UK 17 73177926 73177926 insertion of <=200bp - C intron_variant ESAD-UK 17 73179099 73179099 single base substitution G A upstream_gene_variant ESAD-UK 17 73181650 73181650 single base substitution G C upstream_gene_variant ESCA-CN 17 73164227 73164227 deletion of <=200bp A - 3_prime_UTR_variant ESCA-CN 17 73164227 73164227 deletion of <=200bp A - downstream_gene_variant LAML-KR 17 73164241 73164241 single base substitution T A 3_prime_UTR_variant LAML-KR 17 73164241 73164241 single base substitution T A downstream_gene_variant LAML-KR 17 73165958 73165958 single base substitution A G intron_variant LAML-KR 17 73181520 73181520 single base substitution G A upstream_gene_variant LGG-US 17 73177151 73177151 single base substitution C G splice_donor_variant LICA-FR 17 73181677 73181677 single base substitution C A upstream_gene_variant LINC-JP 17 73170738 73170738 single base substitution T C intron_variant LINC-JP 17 73170838 73170838 deletion of <=200bp T - intron_variant LINC-JP 17 73177907 73177907 single base substitution A C intron_variant LINC-JP 17 73179931 73179931 single base substitution C T upstream_gene_variant LINC-JP 17 73182546 73182546 single base substitution G A upstream_gene_variant LIRI-JP 17 73165868 73165868 single base substitution C G intron_variant LIRI-JP 17 73169455 73169455 single base substitution A C intron_variant LIRI-JP 17 73169619 73169619 single base substitution G T intron_variant LIRI-JP 17 73170472 73170472 single base substitution T C intron_variant LIRI-JP 17 73170982 73170982 single base substitution T C intron_variant LIRI-JP 17 73172018 73172018 single base substitution G A intron_variant LIRI-JP 17 73172081 73172081 single base substitution T C intron_variant LIRI-JP 17 73172828 73172828 single base substitution C T intron_variant LIRI-JP 17 73173991 73173991 single base substitution G C intron_variant LIRI-JP 17 73175695 73175695 single base substitution A C intron_variant LIRI-JP 17 73177195 73177195 single base substitution T C 5_prime_UTR_variant LIRI-JP 17 73177195 73177195 single base substitution T C missense_variant H37R 110A>G LIRI-JP 17 73179705 73179705 single base substitution C T upstream_gene_variant LIRI-JP 17 73181983 73181983 single base substitution G A upstream_gene_variant LIRI-JP 17 73183631 73183631 single base substitution C A upstream_gene_variant LIRI-JP 17 73183814 73183814 single base substitution C A upstream_gene_variant LUSC-KR 17 73160971 73160971 single base substitution T C downstream_gene_variant LUSC-KR 17 73164280 73164280 single base substitution C A 3_prime_UTR_variant LUSC-KR 17 73164280 73164280 single base substitution C A downstream_gene_variant LUSC-KR 17 73168122 73168122 single base substitution G T intron_variant LUSC-KR 17 73172648 73172648 single base substitution T C intron_variant LUSC-KR 17 73172954 73172954 single base substitution G A intron_variant LUSC-KR 17 73173709 73173709 single base substitution G A intron_variant MALY-DE 17 73159157 73159157 single base substitution A G downstream_gene_variant MALY-DE 17 73168088 73168088 single base substitution T A intron_variant MALY-DE 17 73168115 73168115 single base substitution T A intron_variant MALY-DE 17 73172737 73172737 single base substitution G A intron_variant MALY-DE 17 73173282 73173282 single base substitution T A intron_variant MALY-DE 17 73176898 73176898 insertion of <=200bp - A intron_variant MELA-AU 17 73159229 73159229 single base substitution G A downstream_gene_variant MELA-AU 17 73161166 73161166 single base substitution T A downstream_gene_variant MELA-AU 17 73161426 73161426 single base substitution C A downstream_gene_variant MELA-AU 17 73162464 73162464 single base substitution G A downstream_gene_variant MELA-AU 17 73162545 73162545 single base substitution G A downstream_gene_variant MELA-AU 17 73162927 73162927 single base substitution C T downstream_gene_variant MELA-AU 17 73162985 73162985 single base substitution G A downstream_gene_variant MELA-AU 17 73163258 73163258 single base substitution G A downstream_gene_variant MELA-AU 17 73163402 73163402 single base substitution G A downstream_gene_variant MELA-AU 17 73163816 73163816 single base substitution G A 3_prime_UTR_variant MELA-AU 17 73163816 73163816 single base substitution G A downstream_gene_variant MELA-AU 17 73163888 73163888 single base substitution G A 3_prime_UTR_variant MELA-AU 17 73163888 73163888 single base substitution G A downstream_gene_variant MELA-AU 17 73164137 73164137 single base substitution G A 3_prime_UTR_variant MELA-AU 17 73164137 73164137 single base substitution G A downstream_gene_variant MELA-AU 17 73164463 73164463 single base substitution A G missense_variant F44L 130T>C MELA-AU 17 73164463 73164463 single base substitution A G missense_variant F63L 187T>C MELA-AU 17 73164463 73164463 single base substitution A G missense_variant F87L 259T>C MELA-AU 17 73164726 73164726 single base substitution G A intron_variant MELA-AU 17 73164970 73164970 single base substitution G A intron_variant MELA-AU 17 73166928 73166929 multiple base substitution (>=2bp and <=200bp) GT AA intron_variant MELA-AU 17 73167917 73167917 single base substitution C G intron_variant MELA-AU 17 73168702 73168702 single base substitution G A intron_variant MELA-AU 17 73168852 73168852 single base substitution G A intron_variant MELA-AU 17 73169385 73169385 single base substitution G A intron_variant MELA-AU 17 73169556 73169556 single base substitution G A intron_variant MELA-AU 17 73169763 73169763 single base substitution G A intron_variant MELA-AU 17 73169860 73169860 single base substitution C A intron_variant MELA-AU 17 73170316 73170316 deletion of <=200bp C - intron_variant MELA-AU 17 73170400 73170400 single base substitution T C intron_variant MELA-AU 17 73170480 73170480 single base substitution C T intron_variant MELA-AU 17 73170643 73170643 single base substitution G A intron_variant MELA-AU 17 73171922 73171922 single base substitution T G intron_variant MELA-AU 17 73171997 73171997 single base substitution G A intron_variant MELA-AU 17 73172134 73172134 single base substitution G A intron_variant MELA-AU 17 73173253 73173253 single base substitution G A intron_variant MELA-AU 17 73173659 73173659 single base substitution C T intron_variant MELA-AU 17 73173794 73173794 single base substitution G A intron_variant MELA-AU 17 73174504 73174504 single base substitution G A intron_variant MELA-AU 17 73175347 73175347 single base substitution G A intron_variant MELA-AU 17 73176626 73176626 single base substitution G A intron_variant MELA-AU 17 73178247 73178247 single base substitution G A intron_variant MELA-AU 17 73178340 73178341 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 17 73179080 73179080 single base substitution C T upstream_gene_variant MELA-AU 17 73179176 73179176 single base substitution C T upstream_gene_variant MELA-AU 17 73179542 73179542 single base substitution A C upstream_gene_variant MELA-AU 17 73179596 73179596 single base substitution G C upstream_gene_variant MELA-AU 17 73180880 73180880 single base substitution C T upstream_gene_variant MELA-AU 17 73180957 73180957 single base substitution G A upstream_gene_variant MELA-AU 17 73181118 73181118 single base substitution G A upstream_gene_variant MELA-AU 17 73181214 73181214 single base substitution G A upstream_gene_variant MELA-AU 17 73182294 73182294 single base substitution G A upstream_gene_variant MELA-AU 17 73182330 73182330 single base substitution C T upstream_gene_variant MELA-AU 17 73182475 73182475 single base substitution C T upstream_gene_variant MELA-AU 17 73182552 73182553 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 17 73182878 73182878 single base substitution C T upstream_gene_variant MELA-AU 17 73183406 73183406 single base substitution C T upstream_gene_variant MELA-AU 17 73183669 73183669 single base substitution G A upstream_gene_variant MELA-AU 17 73183763 73183763 single base substitution G A upstream_gene_variant ORCA-IN 17 73166558 73166558 single base substitution G A intron_variant OV-AU 17 73163082 73163082 single base substitution C G downstream_gene_variant OV-AU 17 73165538 73165538 single base substitution G T intron_variant OV-AU 17 73175139 73175139 single base substitution G A intron_variant OV-AU 17 73177937 73177937 single base substitution T C intron_variant OV-AU 17 73179974 73179974 single base substitution C A upstream_gene_variant OV-AU 17 73183227 73183227 single base substitution C T upstream_gene_variant PACA-AU 17 73161441 73161441 single base substitution G A downstream_gene_variant PACA-AU 17 73161989 73161989 single base substitution C T downstream_gene_variant PACA-AU 17 73162783 73162786 deletion of <=200bp AGGG - downstream_gene_variant PACA-AU 17 73164679 73164679 deletion of <=200bp T - intron_variant PACA-AU 17 73183410 73183410 single base substitution A G upstream_gene_variant PACA-CA 17 73177482 73177487 deletion of <=200bp GATACG - intron_variant PACA-CA 17 73178153 73178153 single base substitution G C intron_variant PACA-CA 17 73179574 73179574 insertion of <=200bp - T upstream_gene_variant PACA-CA 17 73180513 73180513 single base substitution G T upstream_gene_variant PACA-CA 17 73182667 73182667 single base substitution C T upstream_gene_variant PACA-CA 17 73182987 73182987 single base substitution T C upstream_gene_variant PAEN-AU 17 73174777 73174777 deletion of <=200bp C - intron_variant PAEN-IT 17 73161815 73161815 single base substitution C A downstream_gene_variant PAEN-IT 17 73169873 73169873 single base substitution C G intron_variant PBCA-DE 17 73174856 73174856 single base substitution G A intron_variant PBCA-DE 17 73175068 73175068 single base substitution C A intron_variant PRAD-CA 17 73167492 73167492 single base substitution C A intron_variant PRAD-UK 17 73173070 73173070 single base substitution G C intron_variant PRAD-UK 17 73181212 73181212 single base substitution G C upstream_gene_variant RECA-EU 17 73168785 73168785 single base substitution G C intron_variant RECA-EU 17 73170855 73170855 single base substitution G T intron_variant RECA-EU 17 73170855 73170855 single base substitution G T missense_variant P30T 88C>A RECA-EU 17 73170855 73170855 single base substitution G T missense_variant P73T 217C>A RECA-EU 17 73171686 73171686 single base substitution A G intron_variant RECA-EU 17 73175374 73175374 single base substitution A C intron_variant SKCA-BR 17 73164039 73164039 single base substitution G A 3_prime_UTR_variant SKCA-BR 17 73164039 73164039 single base substitution G A downstream_gene_variant SKCA-BR 17 73166826 73166826 single base substitution T C intron_variant SKCA-BR 17 73168419 73168419 insertion of <=200bp - ACTT intron_variant SKCA-BR 17 73168420 73168420 insertion of <=200bp - CTTCT intron_variant SKCA-BR 17 73173209 73173209 single base substitution G C intron_variant SKCA-BR 17 73173704 73173704 single base substitution G A intron_variant SKCA-BR 17 73178079 73178079 single base substitution T G intron_variant SKCA-BR 17 73178273 73178273 single base substitution G A intron_variant SKCA-BR 17 73181090 73181090 single base substitution T C upstream_gene_variant SKCA-BR 17 73181212 73181212 single base substitution G T upstream_gene_variant SKCA-BR 17 73183067 73183067 single base substitution C T upstream_gene_variant SKCM-US 17 73164463 73164463 single base substitution A G missense_variant F44L 130T>C SKCM-US 17 73164463 73164463 single base substitution A G missense_variant F63L 187T>C SKCM-US 17 73164463 73164463 single base substitution A G missense_variant F87L 259T>C SKCM-US 17 73170892 73170892 single base substitution G A intron_variant SKCM-US 17 73170892 73170892 single base substitution G A synonymous_variant F17F 51C>T SKCM-US 17 73170892 73170892 single base substitution G A synonymous_variant F60F 180C>T THCA-SA 17 73179068 73179068 single base substitution C A 5_prime_UTR_variant THCA-SA 17 73179068 73179068 single base substitution C A upstream_gene_variant UCEC-US 17 73177159 73177159 single base substitution T G missense_variant E49A 146A>C UCEC-US 17 73177159 73177159 single base substitution T G missense_variant E6A 17A>C

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand RK223_C01 COSM4943645 c.110A>G p.H37R Substitution - Missense 17:75181100-75181100 - TCGA-DK-A3X1-01 COSM3796073 c.282C>G p.V94V Substitution - coding silent 17:75168345-75168345 - PD4203a COSM164692 c.205G>A p.E69K Substitution - Missense 17:75174772-75174772 - TCGA-FS-A1ZZ-06 COSM3522046 c.180C>T p.F60F Substitution - coding silent 17:75174797-75174797 - TCGA-AB-2849-03 COSM1318456 c.278G>A p.G93D Substitution - Missense 17:75168349-75168349 - C0071T COSM4422410 c.217C>A p.P73T Substitution - Missense 17:75174760-75174760 - TCGA-BS-A0UV-01 COSM984282 c.146A>C p.E49A Substitution - Missense 17:75181064-75181064 - TCGA-DK-A2I4-01 COSM3796074 c.261C>G p.F87L Substitution - Missense 17:75168366-75168366 - DN110CD COSM5779884 c.278G>C p.G93A Substitution - Missense 17:75168349-75168349 - TCGA-DU-7019-01 COSM3970310 c.153+1G>C p.? Unknown 17:75181056-75181056 - Patient_1 COSM5414172 c.234G>A p.M78I Substitution - Missense 17:75168393-75168393 - Pat_04_A COSM5853459 c.17_18CC>AT p.P6H Substitution - Missense 17:75182817-75182818 - PD13162a COSM5779884 c.278G>C p.G93A Substitution - Missense 17:75168349-75168349 - TCGA-EE-A3AB-06 COSM3522045 c.259T>C p.F87L Substitution - Missense 17:75168368-75168368 - TCGA-AR-A2LE-01 COSM3820531 c.36T>A p.T12T Substitution - coding silent 17:75181174-75181174 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.380956;Hs.380973 17q25.1 603042 2434017|CGAP|BC008450|C/T|non-coding||539|Candidate; 2434017|CGAP|BC016775|C/T|non-coding||553|Candidate; 2434017|CGAP|BC022340|C/T|non-coding||523|Candidate; 2434017|CGAP|BC062713|C/T|non-coding||486|Candidate; 2434017|CGAP|BC068465|C/T|non-coding||538|Candidate; 2434017|CGAP|BC070159|C/T|non-coding||546|Candidate; 2434017|CGAP|BC071645|C/T|non-coding||479|Candidate; 2434017|CGAP|BC071646|C/T|non-coding||515|Candidate; 2434017|CGAP|BC107853|C/T|non-coding||476|Candidate; 2473677|CGAP|BC008450|C/T|non-coding||539|Candidate; 2473677|CGAP|BC016775|C/T|non-coding||553|Candidate; 2473677|CGAP|BC022340|C/T|non-coding||523|Candidate; 2473677|CGAP|BC062713|C/T|non-coding||486|Candidate; 2473677|CGAP|BC068465|C/T|non-coding||538|Candidate; 2473677|CGAP|BC070159|C/T|non-coding||546|Candidate; 2473677|CGAP|BC071645|C/T|non-coding||479|Candidate; 2473677|CGAP|BC071646|C/T|non-coding||515|Candidate; 2473677|CGAP|BC107853|C/T|non-coding||476|Candidate Hs.546298 17q25.1 603042 2434017|CGAP|BC008450|C/T|non-coding||539|Candidate; 2434017|CGAP|BC016775|C/T|non-coding||553|Candidate; 2434017|CGAP|BC022340|C/T|non-coding||523|Candidate; 2434017|CGAP|BC062713|C/T|non-coding||486|Candidate; 2434017|CGAP|BC068465|C/T|non-coding||538|Candidate; 2434017|CGAP|BC070159|C/T|non-coding||546|Candidate; 2434017|CGAP|BC071645|C/T|non-coding||479|Candidate; 2434017|CGAP|BC071646|C/T|non-coding||515|Candidate; 2434017|CGAP|BC107853|C/T|non-coding||476|Candidate; 2473677|CGAP|BC008450|C/T|non-coding||539|Candidate; 2473677|CGAP|BC016775|C/T|non-coding||553|Candidate; 2473677|CGAP|BC022340|C/T|non-coding||523|Candidate; 2473677|CGAP|BC062713|C/T|non-coding||486|Candidate; 2473677|CGAP|BC068465|C/T|non-coding||538|Candidate; 2473677|CGAP|BC070159|C/T|non-coding||546|Candidate; 2473677|CGAP|BC071645|C/T|non-coding||479|Candidate; 2473677|CGAP|BC071646|C/T|non-coding||515|Candidate; 2473677|CGAP|BC107853|C/T|non-coding||476|Candidate

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G Missense p.F87L c.259T>C 17 73164463 CM C G SpliceDonorSNV . c.153+1G>C 17 73177151 LGG C T Missense p.E69K c.205G>A 17 73170867 BRCA G A Synonymous p.F60F c.180C>T 17 73170892 CM G C Missense p.F87L c.261C>G 17 73164461 BLCA - TA Frameshift p.N68Sfs*89 c.199_200dupAT 17 73170872 AML T G IntronicSNV . c.225+1274A>C 17 73169573 CLL