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 10 94109544 94109544 + Missense_Mutation SNP G G A TCGA-C4-A0EZ-01A-21D-A10S-08 TCGA-C4-A0EZ-10A-01D-A10S-08 g.chr10:94109544G>A c.670G>A c.(670-672)Ggt>Agt p.G224S BRCA 10 94070920 94070920 + Missense_Mutation SNP G G A TCGA-D8-A1JA-01A-11D-A13L-09 TCGA-D8-A1JA-10A-01W-A14R-09 g.chr10:94070920G>A c.64G>A c.(64-66)Gaa>Aaa p.E22K BRCA 10 94070926 94070926 + Missense_Mutation SNP G G C TCGA-D8-A1JA-01A-11D-A13L-09 TCGA-D8-A1JA-10A-01W-A14R-09 g.chr10:94070926G>C c.70G>C c.(70-72)Gat>Cat p.D24H BRCA 10 94071041 94071041 + Missense_Mutation SNP G G C TCGA-D8-A1JA-01A-11D-A13L-09 TCGA-D8-A1JA-10A-01W-A14R-09 g.chr10:94071041G>C c.185G>C c.(184-186)aGa>aCa p.R62T BRCA 10 94109244 94109244 + Missense_Mutation SNP C C T TCGA-A8-A09Q-01A-11W-A019-09 TCGA-A8-A09Q-10A-01W-A021-09 g.chr10:94109244C>T c.508C>T c.(508-510)Cgc>Tgc p.R170C BRCA 10 94109244 94109244 + Missense_Mutation SNP C C T TCGA-D8-A1Y1-01A-21D-A14K-09 TCGA-D8-A1Y1-10A-01D-A14K-09 g.chr10:94109244C>T c.508C>T c.(508-510)Cgc>Tgc p.R170C BRCA 10 94110927 94110927 + Missense_Mutation SNP G G A TCGA-E2-A1AZ-01A-11D-A12Q-09 TCGA-E2-A1AZ-10A-01D-A12Q-09 g.chr10:94110927G>A c.800G>A c.(799-801)cGc>cAc p.R267H CESC 10 94070946 94070946 + Silent SNP G G A TCGA-JX-A3Q0-01A-11D-A21Q-09 TCGA-JX-A3Q0-10A-01D-A21Q-09 g.chr10:94070946G>A c.90G>A c.(88-90)gtG>gtA p.V30V COAD 10 94070898 94070898 + Silent SNP C C T TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr10:94070898C>T c.42C>T c.(40-42)tgC>tgT p.C14C COAD 10 94070923 94070925 + In_Frame_Del DEL GAT GAT - TCGA-CK-6747-01A-11D-1835-10 TCGA-CK-6747-10A-01D-1835-10 g.chr10:94070923_94070925delGAT c.67_69delGAT c.(67-69)gatdel p.D24del COAD 10 94100498 94100498 + Nonsense_Mutation SNP G G T TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr10:94100498G>T c.307G>T c.(307-309)Gga>Tga p.G103* COAD 10 94100536 94100536 + Silent SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:94100536T>G c.345T>G c.(343-345)acT>acG p.T115T COAD 10 94109478 94109478 + Missense_Mutation SNP G G T TCGA-AZ-6608-01A-11D-1835-10 TCGA-AZ-6608-11A-01D-1835-10 g.chr10:94109478G>T c.604G>T c.(604-606)Gat>Tat p.D202Y COAD 10 94109478 94109478 + Missense_Mutation SNP G G T TCGA-CK-6748-01A-11D-1835-10 TCGA-CK-6748-10A-01D-1835-10 g.chr10:94109478G>T c.604G>T c.(604-606)Gat>Tat p.D202Y COAD 10 94109479 94109479 + Missense_Mutation SNP A A G TCGA-CM-6168-01A-11D-1650-10 TCGA-CM-6168-10A-01D-1650-10 g.chr10:94109479A>G c.605A>G c.(604-606)gAt>gGt p.D202G COAD 10 94110875 94110875 + Nonsense_Mutation SNP G G T TCGA-A6-2672-01A-01W-0833-10 TCGA-A6-2672-10A-01W-0833-10 g.chr10:94110875G>T c.748G>T c.(748-750)Gga>Tga p.G250* COADREAD 10 94070898 94070898 + Silent SNP C C T TCGA-F4-6856-01A-11D-1924-10 TCGA-F4-6856-10A-01D-1924-10 g.chr10:94070898C>T c.42C>T c.(40-42)tgC>tgT p.C14C COADREAD 10 94070923 94070925 + In_Frame_Del DEL GAT GAT - TCGA-CK-6747-01A-11D-1835-10 TCGA-CK-6747-10A-01D-1835-10 g.chr10:94070923_94070925delGAT c.67_69delGAT c.(67-69)gatdel p.D24del COADREAD 10 94100498 94100498 + Nonsense_Mutation SNP G G T TCGA-AA-3950-01A-02W-0995-10 TCGA-AA-3950-10A-01W-0995-10 g.chr10:94100498G>T c.307G>T c.(307-309)Gga>Tga p.G103* COADREAD 10 94100536 94100536 + Silent SNP T T G TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr10:94100536T>G c.345T>G c.(343-345)acT>acG p.T115T COADREAD 10 94109478 94109478 + Missense_Mutation SNP G G T TCGA-AZ-6608-01A-11D-1835-10 TCGA-AZ-6608-11A-01D-1835-10 g.chr10:94109478G>T c.604G>T c.(604-606)Gat>Tat p.D202Y COADREAD 10 94109478 94109478 + Missense_Mutation SNP G G T TCGA-CK-6748-01A-11D-1835-10 TCGA-CK-6748-10A-01D-1835-10 g.chr10:94109478G>T c.604G>T c.(604-606)Gat>Tat p.D202Y COADREAD 10 94109479 94109479 + Missense_Mutation SNP A A G TCGA-CM-6168-01A-11D-1650-10 TCGA-CM-6168-10A-01D-1650-10 g.chr10:94109479A>G c.605A>G c.(604-606)gAt>gGt p.D202G COADREAD 10 94110875 94110875 + Nonsense_Mutation SNP G G T TCGA-A6-2672-01A-01W-0833-10 TCGA-A6-2672-10A-01W-0833-10 g.chr10:94110875G>T c.748G>T c.(748-750)Gga>Tga p.G250* GBMLGG 10 94109579 94109579 + Silent SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:94109579A>G c.705A>G c.(703-705)ttA>ttG p.L235L GBMLGG 10 94110927 94110927 + Missense_Mutation SNP G G A TCGA-TQ-A7RQ-01A-11D-A33T-08 TCGA-TQ-A7RQ-10A-01D-A33W-08 g.chr10:94110927G>A c.800G>A c.(799-801)cGc>cAc p.R267H HNSC 10 94109493 94109493 + Missense_Mutation SNP A A G TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr10:94109493A>G c.619A>G c.(619-621)Act>Gct p.T207A HNSC 10 94109572 94109572 + Missense_Mutation SNP C C A TCGA-BA-5559-01A-01D-1512-08 TCGA-BA-5559-10A-01D-1512-08 g.chr10:94109572C>A c.698C>A c.(697-699)tCt>tAt p.S233Y KICH 10 94071001 94071001 + Missense_Mutation SNP C C T TCGA-KL-8331-01A-11D-2310-10 TCGA-KL-8331-11A-01D-2310-10 g.chr10:94071001C>T c.145C>T c.(145-147)Cgc>Tgc p.R49C KIPAN 10 94071001 94071001 + Missense_Mutation SNP C C T TCGA-KL-8331-01A-11D-2310-10 TCGA-KL-8331-11A-01D-2310-10 g.chr10:94071001C>T c.145C>T c.(145-147)Cgc>Tgc p.R49C KIPAN 10 94109483 94109483 + Missense_Mutation SNP T T G TCGA-B0-5692-01A-11D-1534-10 TCGA-B0-5692-11A-01D-1534-10 g.chr10:94109483T>G c.609T>G c.(607-609)caT>caG p.H203Q KIPAN 10 94110949 94110949 + Missense_Mutation SNP A A T TCGA-CZ-5463-01A-01D-1501-10 TCGA-CZ-5463-11A-01D-1501-10 g.chr10:94110949A>T c.822A>T c.(820-822)gaA>gaT p.E274D KIRC 10 94109483 94109483 + Missense_Mutation SNP T T G TCGA-B0-5692-01A-11D-1534-10 TCGA-B0-5692-11A-01D-1534-10 g.chr10:94109483T>G c.609T>G c.(607-609)caT>caG p.H203Q KIRC 10 94110949 94110949 + Missense_Mutation SNP A A T TCGA-CZ-5463-01A-01D-1501-10 TCGA-CZ-5463-11A-01D-1501-10 g.chr10:94110949A>T c.822A>T c.(820-822)gaA>gaT p.E274D LGG 10 94109579 94109579 + Silent SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr10:94109579A>G c.705A>G c.(703-705)ttA>ttG p.L235L LGG 10 94110927 94110927 + Missense_Mutation SNP G G A TCGA-TQ-A7RQ-01A-11D-A33T-08 TCGA-TQ-A7RQ-10A-01D-A33W-08 g.chr10:94110927G>A c.800G>A c.(799-801)cGc>cAc p.R267H LIHC 10 94109142 94109142 + Missense_Mutation SNP A A G TCGA-BC-A3KF-01A-11D-A20W-10 TCGA-BC-A3KF-10A-01D-A20W-10 g.chr10:94109142A>G c.406A>G c.(406-408)Aga>Gga p.R136G LIHC 10 94110929 94110929 + Frame_Shift_Del DEL A A - TCGA-G3-A3CJ-01A-11D-A20W-10 TCGA-G3-A3CJ-10A-01D-A20W-10 g.chr10:94110929delA c.802delA c.(802-804)aaafs p.K268fs LUAD 10 94100552 94100552 + Missense_Mutation SNP G G T TCGA-44-5644-01A-21D-2036-08 TCGA-44-5644-10A-01D-2036-08 g.chr10:94100552G>T c.361G>T c.(361-363)Gtg>Ttg p.V121L LUSC 10 94109448 94109448 + Silent SNP C C A TCGA-66-2795-01A-02D-0983-08 TCGA-66-2795-11A-01D-0983-08 g.chr10:94109448C>A c.574C>A c.(574-576)Cga>Aga p.R192R PAAD 10 94109589 94109589 + Missense_Mutation SNP A A G TCGA-2J-AAB4-01A-12D-A40W-08 TCGA-2J-AAB4-10A-01D-A40W-08 g.chr10:94109589A>G c.715A>G c.(715-717)Atc>Gtc p.I239V PAAD 10 94110927 94110927 + Missense_Mutation SNP G G A TCGA-FZ-5922-01A-11D-1609-08 TCGA-FZ-5922-11A-01D-1609-08 g.chr10:94110927G>A c.800G>A c.(799-801)cGc>cAc p.R267H PAAD 10 94110927 94110927 + Missense_Mutation SNP G G A TCGA-IB-AAUU-01A-11D-A377-08 TCGA-IB-AAUU-10A-01D-A37A-08 g.chr10:94110927G>A c.800G>A c.(799-801)cGc>cAc p.R267H PCPG 10 94109245 94109245 + Missense_Mutation SNP G G A TCGA-S7-A7WN-01A-12D-A35I-08 TCGA-S7-A7WN-10A-01D-A35G-08 g.chr10:94109245G>A c.509G>A c.(508-510)cGc>cAc p.R170H PRAD 10 94109442 94109442 + Missense_Mutation SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr10:94109442G>A c.568G>A c.(568-570)Gtt>Att p.V190I SKCM 10 94109449 94109449 + Missense_Mutation SNP G G A TCGA-EE-A29M-06A-11D-A196-08 TCGA-EE-A29M-10A-01D-A198-08 g.chr10:94109449G>A c.575G>A c.(574-576)cGa>cAa p.R192Q SKCM 10 94109519 94109519 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr10:94109519C>T c.645C>T c.(643-645)gtC>gtT p.V215V

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BOCA-FR 10 94055963 94055963 single base substitution G A intron_variant BOCA-FR 10 94090194 94090194 single base substitution G A intron_variant BOCA-FR 10 94090194 94090194 single base substitution G A upstream_gene_variant BOCA-FR 10 94111041 94111041 single base substitution C T 3_prime_UTR_variant BOCA-FR 10 94111041 94111041 single base substitution C T downstream_gene_variant BRCA-EU 10 94047398 94047398 single base substitution G A upstream_gene_variant BRCA-EU 10 94049023 94049023 single base substitution G A upstream_gene_variant BRCA-EU 10 94051083 94051083 single base substitution C T 5_prime_UTR_variant BRCA-EU 10 94051140 94051140 single base substitution C A 5_prime_UTR_variant BRCA-EU 10 94054179 94054179 deletion of <=200bp T - intron_variant BRCA-EU 10 94054791 94054791 deletion of <=200bp A - intron_variant BRCA-EU 10 94055008 94055008 single base substitution A G intron_variant BRCA-EU 10 94058038 94058038 single base substitution C T intron_variant BRCA-EU 10 94062219 94062219 deletion of <=200bp G - intron_variant BRCA-EU 10 94065436 94065436 single base substitution T A intron_variant BRCA-EU 10 94065436 94065436 single base substitution T A upstream_gene_variant BRCA-EU 10 94065754 94065754 single base substitution C T intron_variant BRCA-EU 10 94065754 94065754 single base substitution C T upstream_gene_variant BRCA-EU 10 94066433 94066433 single base substitution A G intron_variant BRCA-EU 10 94066433 94066433 single base substitution A G upstream_gene_variant BRCA-EU 10 94067563 94067563 single base substitution G T intron_variant BRCA-EU 10 94067563 94067563 single base substitution G T upstream_gene_variant BRCA-EU 10 94067703 94067703 single base substitution T C intron_variant BRCA-EU 10 94067703 94067703 single base substitution T C upstream_gene_variant BRCA-EU 10 94069716 94069716 single base substitution G C intron_variant BRCA-EU 10 94070058 94070058 single base substitution G C intron_variant BRCA-EU 10 94072787 94072787 single base substitution T C intron_variant BRCA-EU 10 94074102 94074102 deletion of <=200bp A - intron_variant BRCA-EU 10 94076175 94076175 single base substitution G C intron_variant BRCA-EU 10 94076267 94076267 single base substitution A C intron_variant BRCA-EU 10 94078911 94078911 single base substitution T A intron_variant BRCA-EU 10 94080517 94080517 single base substitution T A intron_variant BRCA-EU 10 94081494 94081494 single base substitution G C intron_variant BRCA-EU 10 94084253 94084253 single base substitution G A intron_variant BRCA-EU 10 94084607 94084607 single base substitution A C intron_variant BRCA-EU 10 94085300 94085300 deletion of <=200bp T - intron_variant BRCA-EU 10 94085542 94085542 single base substitution C T intron_variant BRCA-EU 10 94086434 94086434 single base substitution A G intron_variant BRCA-EU 10 94087193 94087193 single base substitution T C intron_variant BRCA-EU 10 94087627 94087628 deletion of <=200bp AA - intron_variant BRCA-EU 10 94087711 94087711 insertion of <=200bp - CA intron_variant BRCA-EU 10 94087746 94087746 single base substitution G A intron_variant BRCA-EU 10 94087768 94087768 single base substitution G A intron_variant BRCA-EU 10 94087829 94087829 single base substitution A T intron_variant BRCA-EU 10 94088664 94088664 single base substitution T C intron_variant BRCA-EU 10 94088664 94088664 single base substitution T C upstream_gene_variant BRCA-EU 10 94089701 94089701 single base substitution C G intron_variant BRCA-EU 10 94089701 94089701 single base substitution C G upstream_gene_variant BRCA-EU 10 94092381 94092381 single base substitution G C intron_variant BRCA-EU 10 94092381 94092381 single base substitution G C upstream_gene_variant BRCA-EU 10 94093866 94093866 single base substitution G C intron_variant BRCA-EU 10 94094354 94094354 single base substitution C G intron_variant BRCA-EU 10 94095002 94095002 single base substitution T C intron_variant BRCA-EU 10 94095979 94095979 single base substitution A T intron_variant BRCA-EU 10 94096281 94096281 single base substitution A T intron_variant BRCA-EU 10 94096328 94096328 single base substitution A C intron_variant BRCA-EU 10 94097231 94097231 single base substitution T C intron_variant BRCA-EU 10 94097342 94097342 single base substitution G T intron_variant BRCA-EU 10 94097432 94097432 single base substitution G A intron_variant BRCA-EU 10 94098802 94098802 single base substitution A T intron_variant BRCA-EU 10 94099905 94099905 single base substitution C T intron_variant BRCA-EU 10 94100616 94100616 deletion of <=200bp T - intron_variant BRCA-EU 10 94104419 94104419 single base substitution G A intron_variant BRCA-EU 10 94104419 94104419 single base substitution G A upstream_gene_variant BRCA-EU 10 94106780 94106780 single base substitution T C intron_variant BRCA-EU 10 94106780 94106780 single base substitution T C upstream_gene_variant BRCA-EU 10 94107203 94107203 single base substitution A G intron_variant BRCA-EU 10 94107203 94107203 single base substitution A G upstream_gene_variant BRCA-EU 10 94108282 94108282 single base substitution G C intron_variant BRCA-EU 10 94108282 94108282 single base substitution G C upstream_gene_variant BRCA-EU 10 94109032 94109032 deletion of <=200bp A - intron_variant BRCA-EU 10 94109032 94109032 deletion of <=200bp A - upstream_gene_variant BRCA-EU 10 94109353 94109353 deletion of <=200bp T - downstream_gene_variant BRCA-EU 10 94109353 94109353 deletion of <=200bp T - intron_variant BRCA-EU 10 94109945 94109945 single base substitution G C downstream_gene_variant BRCA-EU 10 94109945 94109945 single base substitution G C exon_variant BRCA-EU 10 94109945 94109945 single base substitution G C intron_variant BRCA-EU 10 94111545 94111545 deletion of <=200bp A - 3_prime_UTR_variant BRCA-EU 10 94111545 94111545 deletion of <=200bp A - downstream_gene_variant BRCA-EU 10 94112674 94112674 single base substitution G C 3_prime_UTR_variant BRCA-EU 10 94112674 94112674 single base substitution G C downstream_gene_variant BRCA-EU 10 94114949 94114949 single base substitution G C downstream_gene_variant BRCA-EU 10 94117026 94117026 insertion of <=200bp - TA downstream_gene_variant BRCA-EU 10 94117306 94117306 single base substitution T C downstream_gene_variant BRCA-EU 10 94117979 94117979 single base substitution G C downstream_gene_variant BRCA-EU 10 94118191 94118191 single base substitution G A downstream_gene_variant BRCA-FR 10 94065436 94065436 single base substitution T A intron_variant BRCA-FR 10 94065436 94065436 single base substitution T A upstream_gene_variant BRCA-FR 10 94076963 94076963 single base substitution G T intron_variant BRCA-FR 10 94085915 94085915 single base substitution G C intron_variant BRCA-FR 10 94087193 94087193 single base substitution T C intron_variant BRCA-FR 10 94088664 94088664 single base substitution T C intron_variant BRCA-FR 10 94088664 94088664 single base substitution T C upstream_gene_variant BRCA-FR 10 94089701 94089701 single base substitution C G intron_variant BRCA-FR 10 94089701 94089701 single base substitution C G upstream_gene_variant BRCA-FR 10 94097342 94097342 single base substitution G T intron_variant BRCA-FR 10 94097432 94097432 single base substitution G A intron_variant BRCA-FR 10 94098505 94098505 single base substitution T C intron_variant BRCA-UK 10 94049199 94049199 single base substitution G A upstream_gene_variant BRCA-UK 10 94055717 94055717 single base substitution C T intron_variant BRCA-UK 10 94058038 94058038 single base substitution C T intron_variant BRCA-UK 10 94073181 94073181 single base substitution G A intron_variant BRCA-UK 10 94104419 94104419 single base substitution G A intron_variant BRCA-UK 10 94104419 94104419 single base substitution G A upstream_gene_variant BRCA-UK 10 94108190 94108190 single base substitution G A intron_variant BRCA-UK 10 94108190 94108190 single base substitution G A upstream_gene_variant BRCA-US 10 94070920 94070920 single base substitution G A exon_variant BRCA-US 10 94070920 94070920 single base substitution G A missense_variant E22K 64G>A BRCA-US 10 94070926 94070926 single base substitution G C exon_variant BRCA-US 10 94070926 94070926 single base substitution G C missense_variant D24H 70G>C BRCA-US 10 94071041 94071041 single base substitution G C exon_variant BRCA-US 10 94071041 94071041 single base substitution G C missense_variant R62T 185G>C BRCA-US 10 94109244 94109244 single base substitution C T downstream_gene_variant BRCA-US 10 94109244 94109244 single base substitution C T exon_variant BRCA-US 10 94109244 94109244 single base substitution C T missense_variant R170C 508C>T BRCA-US 10 94110927 94110927 single base substitution G A downstream_gene_variant BRCA-US 10 94110927 94110927 single base substitution G A missense_variant R267H 800G>A BTCA-JP 10 94100444 94100444 single base substitution G A exon_variant BTCA-JP 10 94100444 94100444 single base substitution G A missense_variant V85I 253G>A CESC-US 10 94070946 94070946 single base substitution G A exon_variant CESC-US 10 94070946 94070946 single base substitution G A synonymous_variant V30V 90G>A CLLE-ES 10 94076724 94076724 single base substitution G T intron_variant CLLE-ES 10 94100408 94100408 single base substitution A G intron_variant COAD-US 10 94070898 94070898 single base substitution C T exon_variant COAD-US 10 94070898 94070898 single base substitution C T synonymous_variant C14C 42C>T COCA-CN 10 94055156 94055156 single base substitution A T intron_variant COCA-CN 10 94055171 94055171 single base substitution A T intron_variant COCA-CN 10 94074406 94074406 single base substitution G A intron_variant COCA-CN 10 94074514 94074514 single base substitution C G intron_variant COCA-CN 10 94082580 94082580 single base substitution C T intron_variant COCA-CN 10 94091334 94091334 single base substitution G A intron_variant COCA-CN 10 94091334 94091334 single base substitution G A upstream_gene_variant COCA-CN 10 94109448 94109448 single base substitution C T downstream_gene_variant COCA-CN 10 94109448 94109448 single base substitution C T exon_variant COCA-CN 10 94109448 94109448 single base substitution C T stop_gained R192* 574C>T EOPC-DE 10 94076741 94076741 single base substitution T G intron_variant ESAD-UK 10 94053822 94053822 single base substitution A T intron_variant ESAD-UK 10 94058438 94058438 single base substitution A G intron_variant ESAD-UK 10 94063856 94063856 single base substitution C T intron_variant ESAD-UK 10 94063856 94063856 single base substitution C T upstream_gene_variant ESAD-UK 10 94065918 94065920 deletion of <=200bp CTT - intron_variant ESAD-UK 10 94065918 94065920 deletion of <=200bp CTT - upstream_gene_variant ESAD-UK 10 94067989 94067989 single base substitution C T intron_variant ESAD-UK 10 94067989 94067989 single base substitution C T upstream_gene_variant ESAD-UK 10 94076663 94076663 single base substitution C T intron_variant ESAD-UK 10 94079346 94079346 single base substitution C T intron_variant ESAD-UK 10 94079608 94079608 single base substitution A C intron_variant ESAD-UK 10 94081597 94081597 deletion of <=200bp T - intron_variant ESAD-UK 10 94084265 94084265 single base substitution C T intron_variant ESAD-UK 10 94087279 94087279 single base substitution A C intron_variant ESAD-UK 10 94087442 94087442 single base substitution C G intron_variant ESAD-UK 10 94091698 94091699 deletion of <=200bp GT - intron_variant ESAD-UK 10 94091698 94091699 deletion of <=200bp GT - upstream_gene_variant ESAD-UK 10 94094889 94094889 single base substitution T C intron_variant ESAD-UK 10 94101242 94101242 single base substitution C T intron_variant ESAD-UK 10 94102063 94102063 single base substitution G A intron_variant ESAD-UK 10 94102175 94102175 single base substitution G C intron_variant ESAD-UK 10 94102697 94102697 single base substitution G A intron_variant ESAD-UK 10 94102914 94102914 single base substitution A G intron_variant ESAD-UK 10 94103586 94103586 single base substitution A C intron_variant ESAD-UK 10 94103713 94103713 single base substitution G C intron_variant ESAD-UK 10 94105285 94105285 single base substitution T C intron_variant ESAD-UK 10 94105285 94105285 single base substitution T C upstream_gene_variant ESAD-UK 10 94105784 94105784 single base substitution C T intron_variant ESAD-UK 10 94105784 94105784 single base substitution C T upstream_gene_variant ESAD-UK 10 94107265 94107265 deletion of <=200bp A - intron_variant ESAD-UK 10 94107265 94107265 deletion of <=200bp A - upstream_gene_variant ESAD-UK 10 94107269 94107269 deletion of <=200bp A - intron_variant ESAD-UK 10 94107269 94107269 deletion of <=200bp A - upstream_gene_variant ESAD-UK 10 94112050 94112071 deletion of <=200bp AAGTATGAAAACAAGAAGTCTT - 3_prime_UTR_variant ESAD-UK 10 94112050 94112071 deletion of <=200bp AAGTATGAAAACAAGAAGTCTT - downstream_gene_variant ESAD-UK 10 94112907 94112907 single base substitution G A 3_prime_UTR_variant ESAD-UK 10 94112907 94112907 single base substitution G A downstream_gene_variant ESAD-UK 10 94113826 94113826 single base substitution T A downstream_gene_variant ESAD-UK 10 94115586 94115586 single base substitution G A downstream_gene_variant ESAD-UK 10 94117085 94117085 single base substitution T A downstream_gene_variant ESAD-UK 10 94117693 94117693 insertion of <=200bp - T downstream_gene_variant ESCA-CN 10 94111659 94111660 deletion of <=200bp GT - 3_prime_UTR_variant ESCA-CN 10 94111659 94111660 deletion of <=200bp GT - downstream_gene_variant KIRC-US 10 94109483 94109483 single base substitution T G downstream_gene_variant KIRC-US 10 94109483 94109483 single base substitution T G exon_variant KIRC-US 10 94109483 94109483 single base substitution T G missense_variant H203Q 609T>G KIRC-US 10 94110949 94110949 single base substitution A T downstream_gene_variant KIRC-US 10 94110949 94110949 single base substitution A T missense_variant E274D 822A>T LAML-KR 10 94079475 94079475 single base substitution A G intron_variant LICA-FR 10 94048212 94048213 deletion of <=200bp AA - upstream_gene_variant LICA-FR 10 94053806 94053806 single base substitution A G intron_variant LICA-FR 10 94063368 94063368 single base substitution G A intron_variant LICA-FR 10 94063368 94063368 single base substitution G A upstream_gene_variant LICA-FR 10 94070948 94070948 single base substitution G A exon_variant LICA-FR 10 94070948 94070948 single base substitution G A missense_variant R31K 92G>A LICA-FR 10 94094060 94094060 single base substitution C G intron_variant LICA-FR 10 94112915 94112915 single base substitution A G 3_prime_UTR_variant LICA-FR 10 94112915 94112915 single base substitution A G downstream_gene_variant LINC-JP 10 94049695 94049695 deletion of <=200bp T - upstream_gene_variant LINC-JP 10 94071087 94071087 single base substitution A G exon_variant LINC-JP 10 94071087 94071087 single base substitution A G synonymous_variant P77P 231A>G LINC-JP 10 94071663 94071663 single base substitution A G intron_variant LINC-JP 10 94072849 94072849 single base substitution G A intron_variant LINC-JP 10 94100453 94100453 single base substitution C G exon_variant LINC-JP 10 94100453 94100453 single base substitution C G missense_variant L88V 262C>G LIRI-JP 10 94046026 94046026 single base substitution T A upstream_gene_variant LIRI-JP 10 94046704 94046704 single base substitution C T upstream_gene_variant LIRI-JP 10 94049670 94049670 single base substitution T G upstream_gene_variant LIRI-JP 10 94050405 94050405 single base substitution C A upstream_gene_variant LIRI-JP 10 94052484 94052484 single base substitution T A intron_variant LIRI-JP 10 94052660 94052660 single base substitution G T intron_variant LIRI-JP 10 94053039 94053039 single base substitution T G intron_variant LIRI-JP 10 94054278 94054278 single base substitution A G intron_variant LIRI-JP 10 94054601 94054601 single base substitution T C intron_variant LIRI-JP 10 94055386 94055386 single base substitution C T intron_variant LIRI-JP 10 94055840 94055840 single base substitution C A intron_variant LIRI-JP 10 94057040 94057040 single base substitution C A intron_variant LIRI-JP 10 94058313 94058313 single base substitution A G intron_variant LIRI-JP 10 94060000 94060000 single base substitution G A intron_variant LIRI-JP 10 94063950 94063950 insertion of <=200bp - ATTA intron_variant LIRI-JP 10 94063950 94063950 insertion of <=200bp - ATTA upstream_gene_variant LIRI-JP 10 94064207 94064207 single base substitution A G intron_variant LIRI-JP 10 94064207 94064207 single base substitution A G upstream_gene_variant LIRI-JP 10 94065099 94065099 single base substitution G A intron_variant LIRI-JP 10 94065099 94065099 single base substitution G A upstream_gene_variant LIRI-JP 10 94066364 94066364 single base substitution A G intron_variant LIRI-JP 10 94066364 94066364 single base substitution A G upstream_gene_variant LIRI-JP 10 94068893 94068893 single base substitution T C intron_variant LIRI-JP 10 94070723 94070723 single base substitution C A intron_variant LIRI-JP 10 94071412 94071412 single base substitution A T intron_variant LIRI-JP 10 94072718 94072718 single base substitution C T intron_variant LIRI-JP 10 94074990 94074990 single base substitution C T intron_variant LIRI-JP 10 94080004 94080004 single base substitution A G intron_variant LIRI-JP 10 94080982 94080982 single base substitution C G intron_variant LIRI-JP 10 94082299 94082299 single base substitution T G intron_variant LIRI-JP 10 94083338 94083338 single base substitution C G intron_variant LIRI-JP 10 94085050 94085050 single base substitution T C intron_variant LIRI-JP 10 94089198 94089198 single base substitution C A intron_variant LIRI-JP 10 94089198 94089198 single base substitution C A upstream_gene_variant LIRI-JP 10 94090180 94090180 single base substitution A T intron_variant LIRI-JP 10 94090180 94090180 single base substitution A T upstream_gene_variant LIRI-JP 10 94092334 94092334 single base substitution A G intron_variant LIRI-JP 10 94092334 94092334 single base substitution A G upstream_gene_variant LIRI-JP 10 94092731 94092731 single base substitution G A intron_variant LIRI-JP 10 94092731 94092731 single base substitution G A upstream_gene_variant LIRI-JP 10 94095074 94095074 single base substitution G T intron_variant LIRI-JP 10 94100408 94100408 single base substitution A G intron_variant LIRI-JP 10 94100443 94100443 single base substitution C T exon_variant LIRI-JP 10 94100443 94100443 single base substitution C T synonymous_variant Y84Y 252C>T LIRI-JP 10 94100630 94100630 single base substitution T G intron_variant LIRI-JP 10 94102809 94102809 single base substitution A G intron_variant LIRI-JP 10 94103124 94103124 single base substitution A G intron_variant LIRI-JP 10 94104678 94104678 single base substitution A G intron_variant LIRI-JP 10 94104678 94104678 single base substitution A G upstream_gene_variant LIRI-JP 10 94106184 94106193 deletion of <=200bp TCTCTTCACT - intron_variant LIRI-JP 10 94106184 94106193 deletion of <=200bp TCTCTTCACT - upstream_gene_variant LIRI-JP 10 94109497 94109497 single base substitution G A downstream_gene_variant LIRI-JP 10 94109497 94109497 single base substitution G A exon_variant LIRI-JP 10 94109497 94109497 single base substitution G A missense_variant R208Q 623G>A LIRI-JP 10 94112906 94112906 single base substitution G A 3_prime_UTR_variant LIRI-JP 10 94112906 94112906 single base substitution G A downstream_gene_variant LIRI-JP 10 94114152 94114152 single base substitution A G downstream_gene_variant LIRI-JP 10 94117281 94117281 single base substitution C A downstream_gene_variant LIRI-JP 10 94118194 94118194 single base substitution A G downstream_gene_variant LUSC-KR 10 94059426 94059426 single base substitution A T intron_variant LUSC-KR 10 94062263 94062263 single base substitution A G intron_variant LUSC-KR 10 94065029 94065029 single base substitution T C intron_variant LUSC-KR 10 94065029 94065029 single base substitution T C upstream_gene_variant LUSC-KR 10 94067920 94067920 single base substitution G C intron_variant LUSC-KR 10 94067920 94067920 single base substitution G C upstream_gene_variant LUSC-KR 10 94069237 94069237 single base substitution A G intron_variant LUSC-KR 10 94073281 94073281 single base substitution A G intron_variant LUSC-KR 10 94079098 94079098 single base substitution G T intron_variant LUSC-KR 10 94088937 94088937 single base substitution G C intron_variant LUSC-KR 10 94088937 94088937 single base substitution G C upstream_gene_variant LUSC-KR 10 94090060 94090060 single base substitution G A intron_variant LUSC-KR 10 94090060 94090060 single base substitution G A upstream_gene_variant LUSC-KR 10 94090297 94090297 single base substitution T C intron_variant LUSC-KR 10 94090297 94090297 single base substitution T C upstream_gene_variant LUSC-KR 10 94100748 94100748 single base substitution A G intron_variant LUSC-KR 10 94106916 94106916 single base substitution C T intron_variant LUSC-KR 10 94106916 94106916 single base substitution C T upstream_gene_variant LUSC-KR 10 94107035 94107035 single base substitution A T intron_variant LUSC-KR 10 94107035 94107035 single base substitution A T upstream_gene_variant LUSC-KR 10 94110706 94110706 single base substitution A G downstream_gene_variant LUSC-KR 10 94110706 94110706 single base substitution A G intron_variant LUSC-KR 10 94115601 94115601 single base substitution G C downstream_gene_variant LUSC-US 10 94109448 94109448 single base substitution C A downstream_gene_variant LUSC-US 10 94109448 94109448 single base substitution C A exon_variant LUSC-US 10 94109448 94109448 single base substitution C A synonymous_variant R192R 574C>A MALY-DE 10 94046352 94046352 single base substitution A C upstream_gene_variant MALY-DE 10 94056609 94056609 single base substitution G C intron_variant MALY-DE 10 94058680 94058680 single base substitution G A intron_variant MALY-DE 10 94060076 94060076 deletion of <=200bp A - intron_variant MALY-DE 10 94064348 94064348 single base substitution T C intron_variant MALY-DE 10 94064348 94064348 single base substitution T C upstream_gene_variant MALY-DE 10 94080790 94080790 single base substitution A G intron_variant MALY-DE 10 94086724 94086724 single base substitution G T intron_variant MALY-DE 10 94086771 94086771 deletion of <=200bp T - intron_variant MALY-DE 10 94098609 94098609 single base substitution A C intron_variant MALY-DE 10 94101513 94101513 single base substitution A T intron_variant MALY-DE 10 94109668 94109668 single base substitution A T downstream_gene_variant MALY-DE 10 94109668 94109668 single base substitution A T exon_variant MALY-DE 10 94109668 94109668 single base substitution A T intron_variant MELA-AU 10 94046415 94046415 single base substitution A G upstream_gene_variant MELA-AU 10 94046871 94046871 single base substitution G A upstream_gene_variant MELA-AU 10 94048419 94048419 single base substitution A T upstream_gene_variant MELA-AU 10 94048872 94048872 single base substitution A T upstream_gene_variant MELA-AU 10 94048892 94048893 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 10 94051303 94051303 single base substitution G A intron_variant MELA-AU 10 94051481 94051481 single base substitution T A intron_variant MELA-AU 10 94052686 94052686 single base substitution C T intron_variant MELA-AU 10 94053405 94053405 single base substitution T A intron_variant MELA-AU 10 94053789 94053789 single base substitution G A intron_variant MELA-AU 10 94055103 94055103 single base substitution G A intron_variant MELA-AU 10 94055605 94055605 single base substitution T A intron_variant MELA-AU 10 94055671 94055671 single base substitution C T intron_variant MELA-AU 10 94056600 94056600 single base substitution G A intron_variant MELA-AU 10 94057221 94057221 single base substitution C T intron_variant MELA-AU 10 94057280 94057280 single base substitution C T intron_variant MELA-AU 10 94057340 94057340 single base substitution C T intron_variant MELA-AU 10 94057703 94057703 single base substitution C T intron_variant MELA-AU 10 94058130 94058130 single base substitution C T intron_variant MELA-AU 10 94059583 94059583 single base substitution C T intron_variant MELA-AU 10 94060684 94060684 single base substitution C T intron_variant MELA-AU 10 94061776 94061776 single base substitution C T intron_variant MELA-AU 10 94062496 94062496 single base substitution C T intron_variant MELA-AU 10 94063841 94063841 single base substitution G A intron_variant MELA-AU 10 94063841 94063841 single base substitution G A upstream_gene_variant MELA-AU 10 94065149 94065149 single base substitution G A intron_variant MELA-AU 10 94065149 94065149 single base substitution G A upstream_gene_variant MELA-AU 10 94065217 94065217 single base substitution T G intron_variant MELA-AU 10 94065217 94065217 single base substitution T G upstream_gene_variant MELA-AU 10 94065476 94065476 single base substitution C T intron_variant MELA-AU 10 94065476 94065476 single base substitution C T upstream_gene_variant MELA-AU 10 94065634 94065634 single base substitution C T intron_variant MELA-AU 10 94065634 94065634 single base substitution C T upstream_gene_variant MELA-AU 10 94065822 94065822 single base substitution C T intron_variant MELA-AU 10 94065822 94065822 single base substitution C T upstream_gene_variant MELA-AU 10 94066342 94066342 single base substitution C T intron_variant MELA-AU 10 94066342 94066342 single base substitution C T upstream_gene_variant MELA-AU 10 94066694 94066694 single base substitution C T intron_variant MELA-AU 10 94066694 94066694 single base substitution C T upstream_gene_variant MELA-AU 10 94066843 94066843 single base substitution A G intron_variant MELA-AU 10 94066843 94066843 single base substitution A G upstream_gene_variant MELA-AU 10 94067000 94067000 single base substitution C T intron_variant MELA-AU 10 94067000 94067000 single base substitution C T upstream_gene_variant MELA-AU 10 94067564 94067564 single base substitution G A intron_variant MELA-AU 10 94067564 94067564 single base substitution G A upstream_gene_variant MELA-AU 10 94067682 94067682 single base substitution G T intron_variant MELA-AU 10 94067682 94067682 single base substitution G T upstream_gene_variant MELA-AU 10 94068208 94068208 single base substitution C T intron_variant MELA-AU 10 94068208 94068208 single base substitution C T upstream_gene_variant MELA-AU 10 94068249 94068249 single base substitution C T exon_variant MELA-AU 10 94068249 94068249 single base substitution C T intron_variant MELA-AU 10 94068466 94068466 single base substitution T G intron_variant MELA-AU 10 94069167 94069167 single base substitution C T intron_variant MELA-AU 10 94074652 94074652 single base substitution C T intron_variant MELA-AU 10 94075165 94075165 single base substitution A T intron_variant MELA-AU 10 94076129 94076129 single base substitution C T intron_variant MELA-AU 10 94076531 94076531 single base substitution C T intron_variant MELA-AU 10 94077150 94077150 single base substitution C T intron_variant MELA-AU 10 94077462 94077462 single base substitution C T intron_variant MELA-AU 10 94078866 94078866 single base substitution C T intron_variant MELA-AU 10 94079397 94079397 single base substitution T C intron_variant MELA-AU 10 94080008 94080008 single base substitution C T intron_variant MELA-AU 10 94080375 94080375 single base substitution T C intron_variant MELA-AU 10 94080952 94080952 single base substitution C T intron_variant MELA-AU 10 94082100 94082100 single base substitution C T intron_variant MELA-AU 10 94082108 94082108 single base substitution C T intron_variant MELA-AU 10 94082514 94082514 single base substitution G T intron_variant MELA-AU 10 94083932 94083932 single base substitution C T intron_variant MELA-AU 10 94084031 94084031 single base substitution C T intron_variant MELA-AU 10 94084241 94084241 single base substitution C T intron_variant MELA-AU 10 94084324 94084324 single base substitution T C intron_variant MELA-AU 10 94084453 94084453 single base substitution C T intron_variant MELA-AU 10 94084611 94084611 single base substitution T A intron_variant MELA-AU 10 94086015 94086015 single base substitution C T intron_variant MELA-AU 10 94086068 94086068 single base substitution A G intron_variant MELA-AU 10 94086541 94086541 single base substitution T A intron_variant MELA-AU 10 94086842 94086842 single base substitution G A intron_variant MELA-AU 10 94087109 94087109 single base substitution T A intron_variant MELA-AU 10 94088360 94088360 single base substitution C T intron_variant MELA-AU 10 94088360 94088360 single base substitution C T upstream_gene_variant MELA-AU 10 94088446 94088446 single base substitution C T intron_variant MELA-AU 10 94088446 94088446 single base substitution C T upstream_gene_variant MELA-AU 10 94089098 94089098 single base substitution C T intron_variant MELA-AU 10 94089098 94089098 single base substitution C T upstream_gene_variant MELA-AU 10 94089155 94089155 single base substitution G A intron_variant MELA-AU 10 94089155 94089155 single base substitution G A upstream_gene_variant MELA-AU 10 94089867 94089867 single base substitution T A intron_variant MELA-AU 10 94089867 94089867 single base substitution T A upstream_gene_variant MELA-AU 10 94090487 94090487 single base substitution C T intron_variant MELA-AU 10 94090487 94090487 single base substitution C T upstream_gene_variant MELA-AU 10 94091394 94091394 single base substitution A G intron_variant MELA-AU 10 94091394 94091394 single base substitution A G upstream_gene_variant MELA-AU 10 94091678 94091678 single base substitution A G intron_variant MELA-AU 10 94091678 94091678 single base substitution A G upstream_gene_variant MELA-AU 10 94091697 94091697 single base substitution C T intron_variant MELA-AU 10 94091697 94091697 single base substitution C T upstream_gene_variant MELA-AU 10 94092193 94092193 single base substitution C T intron_variant MELA-AU 10 94092193 94092193 single base substitution C T upstream_gene_variant MELA-AU 10 94092474 94092474 single base substitution C T intron_variant MELA-AU 10 94092474 94092474 single base substitution C T upstream_gene_variant MELA-AU 10 94092886 94092886 single base substitution C T intron_variant MELA-AU 10 94092886 94092886 single base substitution C T upstream_gene_variant MELA-AU 10 94092909 94092909 single base substitution C T intron_variant MELA-AU 10 94092909 94092909 single base substitution C T upstream_gene_variant MELA-AU 10 94092999 94092999 single base substitution C T intron_variant MELA-AU 10 94092999 94092999 single base substitution C T upstream_gene_variant MELA-AU 10 94093056 94093056 single base substitution G T intron_variant MELA-AU 10 94093056 94093056 single base substitution G T upstream_gene_variant MELA-AU 10 94093313 94093313 single base substitution A G exon_variant MELA-AU 10 94093313 94093313 single base substitution A G intron_variant MELA-AU 10 94093726 94093726 single base substitution C T intron_variant MELA-AU 10 94093775 94093775 single base substitution C T intron_variant MELA-AU 10 94095758 94095758 single base substitution A G intron_variant MELA-AU 10 94095772 94095772 single base substitution C T intron_variant MELA-AU 10 94096052 94096052 single base substitution C T intron_variant MELA-AU 10 94096062 94096062 single base substitution G A intron_variant MELA-AU 10 94096107 94096107 single base substitution C T intron_variant MELA-AU 10 94097393 94097393 single base substitution T A intron_variant MELA-AU 10 94098290 94098290 single base substitution T C intron_variant MELA-AU 10 94099254 94099254 single base substitution C T intron_variant MELA-AU 10 94100367 94100367 single base substitution C T intron_variant MELA-AU 10 94100925 94100925 single base substitution C T intron_variant MELA-AU 10 94101167 94101167 single base substitution A T intron_variant MELA-AU 10 94101813 94101813 single base substitution C T intron_variant MELA-AU 10 94103209 94103209 single base substitution C T intron_variant MELA-AU 10 94103276 94103276 single base substitution C T intron_variant MELA-AU 10 94103441 94103441 single base substitution C T intron_variant MELA-AU 10 94104784 94104784 single base substitution C T intron_variant MELA-AU 10 94104784 94104784 single base substitution C T upstream_gene_variant MELA-AU 10 94105778 94105778 single base substitution C T intron_variant MELA-AU 10 94105778 94105778 single base substitution C T upstream_gene_variant MELA-AU 10 94106101 94106101 single base substitution A T intron_variant MELA-AU 10 94106101 94106101 single base substitution A T upstream_gene_variant MELA-AU 10 94106849 94106849 single base substitution C T intron_variant MELA-AU 10 94106849 94106849 single base substitution C T upstream_gene_variant MELA-AU 10 94106961 94106961 single base substitution C T intron_variant MELA-AU 10 94106961 94106961 single base substitution C T upstream_gene_variant MELA-AU 10 94106989 94106989 single base substitution C T intron_variant MELA-AU 10 94106989 94106989 single base substitution C T upstream_gene_variant MELA-AU 10 94107214 94107214 single base substitution C T intron_variant MELA-AU 10 94107214 94107214 single base substitution C T upstream_gene_variant MELA-AU 10 94107326 94107326 single base substitution C T intron_variant MELA-AU 10 94107326 94107326 single base substitution C T upstream_gene_variant MELA-AU 10 94107368 94107368 single base substitution T G intron_variant MELA-AU 10 94107368 94107368 single base substitution T G upstream_gene_variant MELA-AU 10 94107511 94107511 single base substitution C T intron_variant MELA-AU 10 94107511 94107511 single base substitution C T upstream_gene_variant MELA-AU 10 94107812 94107814 deletion of <=200bp CAC - intron_variant MELA-AU 10 94107812 94107814 deletion of <=200bp CAC - upstream_gene_variant MELA-AU 10 94107937 94107937 single base substitution C T intron_variant MELA-AU 10 94107937 94107937 single base substitution C T upstream_gene_variant MELA-AU 10 94109159 94109159 single base substitution C T exon_variant MELA-AU 10 94109159 94109159 single base substitution C T synonymous_variant F141F 423C>T MELA-AU 10 94109159 94109159 single base substitution C T upstream_gene_variant MELA-AU 10 94109421 94109421 single base substitution C T downstream_gene_variant MELA-AU 10 94109421 94109421 single base substitution C T intron_variant MELA-AU 10 94109421 94109421 single base substitution C T splice_region_variant MELA-AU 10 94110096 94110096 single base substitution G A downstream_gene_variant MELA-AU 10 94110096 94110096 single base substitution G A intron_variant MELA-AU 10 94111027 94111027 single base substitution C T 3_prime_UTR_variant MELA-AU 10 94111027 94111027 single base substitution C T downstream_gene_variant MELA-AU 10 94111122 94111122 single base substitution C T 3_prime_UTR_variant MELA-AU 10 94111122 94111122 single base substitution C T downstream_gene_variant MELA-AU 10 94111292 94111292 single base substitution C T 3_prime_UTR_variant MELA-AU 10 94111292 94111292 single base substitution C T downstream_gene_variant MELA-AU 10 94112679 94112679 single base substitution C T 3_prime_UTR_variant MELA-AU 10 94112679 94112679 single base substitution C T downstream_gene_variant MELA-AU 10 94112750 94112750 single base substitution C T 3_prime_UTR_variant MELA-AU 10 94112750 94112750 single base substitution C T downstream_gene_variant MELA-AU 10 94114309 94114309 single base substitution C T downstream_gene_variant MELA-AU 10 94114903 94114903 single base substitution C T downstream_gene_variant MELA-AU 10 94114991 94114991 single base substitution C T downstream_gene_variant MELA-AU 10 94115201 94115201 single base substitution C T downstream_gene_variant MELA-AU 10 94115627 94115627 single base substitution C T downstream_gene_variant MELA-AU 10 94116015 94116015 single base substitution G A downstream_gene_variant MELA-AU 10 94116148 94116148 single base substitution A G downstream_gene_variant MELA-AU 10 94116468 94116468 single base substitution T C downstream_gene_variant MELA-AU 10 94116625 94116625 single base substitution G A downstream_gene_variant MELA-AU 10 94116924 94116925 deletion of <=200bp CT - downstream_gene_variant MELA-AU 10 94118505 94118505 single base substitution C T downstream_gene_variant ORCA-IN 10 94046243 94046243 single base substitution G A upstream_gene_variant ORCA-IN 10 94057934 94057935 deletion of <=200bp TA - intron_variant ORCA-IN 10 94058508 94058508 single base substitution C T intron_variant ORCA-IN 10 94061645 94061645 single base substitution A G intron_variant ORCA-IN 10 94068938 94068938 single base substitution T C intron_variant ORCA-IN 10 94081557 94081557 single base substitution G A intron_variant ORCA-IN 10 94102696 94102696 single base substitution G A intron_variant OV-AU 10 94046211 94046211 single base substitution G T upstream_gene_variant OV-AU 10 94050906 94050906 single base substitution A T upstream_gene_variant OV-AU 10 94059318 94059318 single base substitution T G intron_variant OV-AU 10 94062704 94062704 single base substitution A G intron_variant OV-AU 10 94065236 94065236 single base substitution C A intron_variant OV-AU 10 94065236 94065236 single base substitution C A upstream_gene_variant OV-AU 10 94065932 94065932 single base substitution T G intron_variant OV-AU 10 94065932 94065932 single base substitution T G upstream_gene_variant OV-AU 10 94065950 94065950 single base substitution G T intron_variant OV-AU 10 94065950 94065950 single base substitution G T upstream_gene_variant OV-AU 10 94070004 94070004 single base substitution T C intron_variant OV-AU 10 94080481 94080481 single base substitution A G intron_variant OV-AU 10 94082845 94082845 single base substitution T C intron_variant OV-AU 10 94088522 94088522 single base substitution G A intron_variant OV-AU 10 94088522 94088522 single base substitution G A upstream_gene_variant OV-AU 10 94088956 94088956 single base substitution G T intron_variant OV-AU 10 94088956 94088956 single base substitution G T upstream_gene_variant OV-AU 10 94091950 94091950 single base substitution A G intron_variant OV-AU 10 94091950 94091950 single base substitution A G upstream_gene_variant OV-AU 10 94099940 94099940 single base substitution G T intron_variant OV-AU 10 94107421 94107421 single base substitution T G intron_variant OV-AU 10 94107421 94107421 single base substitution T G upstream_gene_variant OV-AU 10 94109031 94109031 single base substitution T G intron_variant OV-AU 10 94109031 94109031 single base substitution T G upstream_gene_variant OV-AU 10 94110770 94110770 single base substitution G T downstream_gene_variant OV-AU 10 94110770 94110770 single base substitution G T intron_variant OV-AU 10 94115528 94115528 single base substitution G A downstream_gene_variant OV-AU 10 94115829 94115829 single base substitution C T downstream_gene_variant PACA-AU 10 94049053 94049053 single base substitution G C upstream_gene_variant PACA-AU 10 94054227 94054227 single base substitution C T intron_variant PACA-AU 10 94055172 94055172 single base substitution T A intron_variant PACA-AU 10 94070917 94070917 single base substitution G A exon_variant PACA-AU 10 94070917 94070917 single base substitution G A missense_variant D21N 61G>A PACA-AU 10 94072671 94072671 single base substitution G A intron_variant PACA-AU 10 94077031 94077031 deletion of <=200bp T - intron_variant PACA-AU 10 94090496 94090496 single base substitution G T intron_variant PACA-AU 10 94090496 94090496 single base substitution G T upstream_gene_variant PACA-AU 10 94092997 94092997 single base substitution T C intron_variant PACA-AU 10 94092997 94092997 single base substitution T C upstream_gene_variant PACA-AU 10 94100459 94100459 single base substitution G C exon_variant PACA-AU 10 94100459 94100459 single base substitution G C missense_variant D90H 268G>C PACA-AU 10 94107215 94107215 single base substitution C T intron_variant PACA-AU 10 94107215 94107215 single base substitution C T upstream_gene_variant PACA-CA 10 94055451 94055451 single base substitution C T intron_variant PACA-CA 10 94068700 94068700 single base substitution G A intron_variant PACA-CA 10 94071879 94071879 single base substitution G T intron_variant PACA-CA 10 94073084 94073084 single base substitution G A intron_variant PACA-CA 10 94078711 94078711 single base substitution G T intron_variant PACA-CA 10 94078712 94078712 single base substitution C T intron_variant PACA-CA 10 94079384 94079384 single base substitution T A intron_variant PACA-CA 10 94080613 94080613 single base substitution G T intron_variant PACA-CA 10 94082303 94082303 single base substitution C G intron_variant PACA-CA 10 94082783 94082783 single base substitution G A intron_variant PACA-CA 10 94082908 94082908 single base substitution C A intron_variant PACA-CA 10 94085669 94085669 single base substitution C G intron_variant PACA-CA 10 94090176 94090176 single base substitution G C intron_variant PACA-CA 10 94090176 94090176 single base substitution G C upstream_gene_variant PACA-CA 10 94091802 94091802 single base substitution G A intron_variant PACA-CA 10 94091802 94091802 single base substitution G A upstream_gene_variant PACA-CA 10 94095446 94095446 deletion of <=200bp T - intron_variant PACA-CA 10 94098007 94098007 single base substitution A G intron_variant PACA-CA 10 94102480 94102480 single base substitution C G intron_variant PACA-CA 10 94107319 94107319 single base substitution G T intron_variant PACA-CA 10 94107319 94107319 single base substitution G T upstream_gene_variant PACA-CA 10 94107959 94107959 single base substitution T A intron_variant PACA-CA 10 94107959 94107959 single base substitution T A upstream_gene_variant PACA-CA 10 94111643 94111643 single base substitution T G 3_prime_UTR_variant PACA-CA 10 94111643 94111643 single base substitution T G downstream_gene_variant PACA-CA 10 94114723 94114723 single base substitution T A downstream_gene_variant PACA-CA 10 94115453 94115453 single base substitution G A downstream_gene_variant PACA-CA 10 94117095 94117095 single base substitution G A downstream_gene_variant PAEN-AU 10 94063247 94063247 single base substitution A G intron_variant PAEN-AU 10 94063247 94063247 single base substitution A G upstream_gene_variant PAEN-IT 10 94093712 94093712 single base substitution C T intron_variant PBCA-DE 10 94055636 94055636 deletion of <=200bp T - intron_variant PBCA-DE 10 94068445 94068445 single base substitution C T intron_variant PBCA-DE 10 94071179 94071179 deletion of <=200bp T - intron_variant PBCA-DE 10 94085560 94085560 single base substitution G A intron_variant PBCA-DE 10 94087110 94087110 single base substitution A T intron_variant PBCA-DE 10 94091647 94091647 insertion of <=200bp - TTTT intron_variant PBCA-DE 10 94091647 94091647 insertion of <=200bp - TTTT upstream_gene_variant PBCA-DE 10 94091698 94091699 deletion of <=200bp GT - intron_variant PBCA-DE 10 94091698 94091699 deletion of <=200bp GT - upstream_gene_variant PBCA-DE 10 94108375 94108375 single base substitution C T intron_variant PBCA-DE 10 94108375 94108375 single base substitution C T upstream_gene_variant PBCA-DE 10 94111440 94111440 single base substitution T A 3_prime_UTR_variant PBCA-DE 10 94111440 94111440 single base substitution T A downstream_gene_variant PBCA-DE 10 94112638 94112638 single base substitution G T 3_prime_UTR_variant PBCA-DE 10 94112638 94112638 single base substitution G T downstream_gene_variant PBCA-DE 10 94113827 94113827 insertion of <=200bp - A downstream_gene_variant PRAD-CA 10 94063276 94063276 single base substitution T G intron_variant PRAD-CA 10 94063276 94063276 single base substitution T G upstream_gene_variant PRAD-CA 10 94092939 94092939 single base substitution G A intron_variant PRAD-CA 10 94092939 94092939 single base substitution G A upstream_gene_variant PRAD-CA 10 94105454 94105454 single base substitution C T intron_variant PRAD-CA 10 94105454 94105454 single base substitution C T upstream_gene_variant PRAD-UK 10 94048685 94048685 single base substitution G C upstream_gene_variant PRAD-UK 10 94052119 94052119 single base substitution C G intron_variant PRAD-UK 10 94078518 94078518 single base substitution C A intron_variant PRAD-UK 10 94110008 94110008 single base substitution A G downstream_gene_variant PRAD-UK 10 94110008 94110008 single base substitution A G exon_variant PRAD-UK 10 94110008 94110008 single base substitution A G intron_variant RECA-EU 10 94062130 94062130 single base substitution C T intron_variant RECA-EU 10 94062371 94062371 single base substitution T A intron_variant RECA-EU 10 94063289 94063289 single base substitution T C intron_variant RECA-EU 10 94063289 94063289 single base substitution T C upstream_gene_variant RECA-EU 10 94066396 94066396 single base substitution A T intron_variant RECA-EU 10 94066396 94066396 single base substitution A T upstream_gene_variant RECA-EU 10 94067499 94067499 single base substitution G C intron_variant RECA-EU 10 94067499 94067499 single base substitution G C upstream_gene_variant RECA-EU 10 94069233 94069233 single base substitution A T intron_variant RECA-EU 10 94083128 94083128 single base substitution A G intron_variant RECA-EU 10 94086901 94086901 single base substitution A G intron_variant RECA-EU 10 94093448 94093448 single base substitution C A intron_variant RECA-EU 10 94096878 94096878 single base substitution C A intron_variant RECA-EU 10 94100510 94100510 single base substitution G A exon_variant RECA-EU 10 94100510 94100510 single base substitution G A missense_variant G107S 319G>A SKCA-BR 10 94047182 94047182 single base substitution G A upstream_gene_variant SKCA-BR 10 94049491 94049491 single base substitution T A upstream_gene_variant SKCA-BR 10 94050097 94050097 single base substitution T C upstream_gene_variant SKCA-BR 10 94052740 94052740 single base substitution A C intron_variant SKCA-BR 10 94053095 94053095 single base substitution C T intron_variant SKCA-BR 10 94055068 94055072 deletion of <=200bp TTTTC - intron_variant SKCA-BR 10 94057490 94057490 single base substitution A C intron_variant SKCA-BR 10 94057923 94057923 insertion of <=200bp - ATC intron_variant SKCA-BR 10 94060648 94060648 insertion of <=200bp - CTT intron_variant SKCA-BR 10 94063338 94063338 single base substitution T C intron_variant SKCA-BR 10 94063338 94063338 single base substitution T C upstream_gene_variant SKCA-BR 10 94064834 94064834 single base substitution G A intron_variant SKCA-BR 10 94064834 94064834 single base substitution G A upstream_gene_variant SKCA-BR 10 94065106 94065106 single base substitution G A intron_variant SKCA-BR 10 94065106 94065106 single base substitution G A upstream_gene_variant SKCA-BR 10 94066965 94066971 deletion of <=200bp TGTGTGC - intron_variant SKCA-BR 10 94066965 94066971 deletion of <=200bp TGTGTGC - upstream_gene_variant SKCA-BR 10 94067266 94067266 single base substitution T G intron_variant SKCA-BR 10 94067266 94067266 single base substitution T G upstream_gene_variant SKCA-BR 10 94071592 94071592 single base substitution C T intron_variant SKCA-BR 10 94071613 94071613 single base substitution T G intron_variant SKCA-BR 10 94078183 94078184 deletion of <=200bp CA - intron_variant SKCA-BR 10 94079052 94079052 single base substitution T C intron_variant SKCA-BR 10 94079054 94079054 insertion of <=200bp - CT intron_variant SKCA-BR 10 94084867 94084867 single base substitution A G intron_variant SKCA-BR 10 94084936 94084936 single base substitution G A intron_variant SKCA-BR 10 94087065 94087065 insertion of <=200bp - CT intron_variant SKCA-BR 10 94088558 94088558 insertion of <=200bp - TTATATATATATATATATATA intron_variant SKCA-BR 10 94088558 94088558 insertion of <=200bp - TTATATATATATATATATATA upstream_gene_variant SKCA-BR 10 94091626 94091646 deletion of <=200bp TTATATATAATCATATATATG - intron_variant SKCA-BR 10 94091626 94091646 deletion of <=200bp TTATATATAATCATATATATG - upstream_gene_variant SKCA-BR 10 94091646 94091646 insertion of <=200bp - GTTTT intron_variant SKCA-BR 10 94091646 94091646 insertion of <=200bp - GTTTT upstream_gene_variant SKCA-BR 10 94092849 94092849 single base substitution G A intron_variant SKCA-BR 10 94092849 94092849 single base substitution G A upstream_gene_variant SKCA-BR 10 94097079 94097079 single base substitution C T intron_variant SKCA-BR 10 94098799 94098799 insertion of <=200bp - CT intron_variant SKCA-BR 10 94098801 94098801 single base substitution C T intron_variant SKCA-BR 10 94099439 94099439 single base substitution A T intron_variant SKCA-BR 10 94106381 94106381 single base substitution G T intron_variant SKCA-BR 10 94106381 94106381 single base substitution G T upstream_gene_variant SKCA-BR 10 94107268 94107273 deletion of <=200bp TAGATA - intron_variant SKCA-BR 10 94107268 94107273 deletion of <=200bp TAGATA - upstream_gene_variant SKCA-BR 10 94107272 94107273 deletion of <=200bp TA - intron_variant SKCA-BR 10 94107272 94107273 deletion of <=200bp TA - upstream_gene_variant SKCA-BR 10 94107277 94107280 deletion of <=200bp AGAT - intron_variant SKCA-BR 10 94107277 94107280 deletion of <=200bp AGAT - upstream_gene_variant SKCA-BR 10 94107942 94107943 deletion of <=200bp CA - intron_variant SKCA-BR 10 94107942 94107943 deletion of <=200bp CA - upstream_gene_variant SKCA-BR 10 94108831 94108831 single base substitution T C intron_variant SKCA-BR 10 94108831 94108831 single base substitution T C upstream_gene_variant SKCA-BR 10 94115302 94115302 single base substitution T G downstream_gene_variant SKCA-BR 10 94117273 94117273 single base substitution T C downstream_gene_variant SKCA-BR 10 94117786 94117786 single base substitution C T downstream_gene_variant SKCM-US 10 94109449 94109449 single base substitution G A downstream_gene_variant SKCM-US 10 94109449 94109449 single base substitution G A exon_variant SKCM-US 10 94109449 94109449 single base substitution G A missense_variant R192Q 575G>A SKCM-US 10 94109519 94109519 single base substitution C T downstream_gene_variant SKCM-US 10 94109519 94109519 single base substitution C T exon_variant SKCM-US 10 94109519 94109519 single base substitution C T synonymous_variant V215V 645C>T STAD-US 10 94070932 94070932 single base substitution A C exon_variant STAD-US 10 94070932 94070932 single base substitution A C missense_variant T26P 76A>C STAD-US 10 94100524 94100524 single base substitution G A exon_variant STAD-US 10 94100524 94100524 single base substitution G A stop_gained W111* 333G>A STAD-US 10 94109437 94109437 single base substitution G T downstream_gene_variant STAD-US 10 94109437 94109437 single base substitution G T exon_variant STAD-US 10 94109437 94109437 single base substitution G T missense_variant C188F 563G>T UCEC-US 10 94070983 94070983 single base substitution C A exon_variant UCEC-US 10 94070983 94070983 single base substitution C A missense_variant H43N 127C>A UCEC-US 10 94071050 94071050 single base substitution G A exon_variant UCEC-US 10 94071050 94071050 single base substitution G A missense_variant C65Y 194G>A UCEC-US 10 94109126 94109126 single base substitution T A exon_variant UCEC-US 10 94109126 94109126 single base substitution T A synonymous_variant G130G 390T>A UCEC-US 10 94109126 94109126 single base substitution T A upstream_gene_variant UCEC-US 10 94109496 94109496 single base substitution C T downstream_gene_variant UCEC-US 10 94109496 94109496 single base substitution C T exon_variant UCEC-US 10 94109496 94109496 single base substitution C T stop_gained R208* 622C>T UCEC-US 10 94109562 94109562 single base substitution A T downstream_gene_variant UCEC-US 10 94109562 94109562 single base substitution A T exon_variant UCEC-US 10 94109562 94109562 single base substitution A T missense_variant S230C 688A>T UCEC-US 10 94109593 94109593 single base substitution T C downstream_gene_variant UCEC-US 10 94109593 94109593 single base substitution T C exon_variant UCEC-US 10 94109593 94109593 single base substitution T C missense_variant L240S 719T>C

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand 8069192 COSM4408249 c.61G>A p.D21N Substitution - Missense 10:92311160-92311160 + Gp5D COSM1969577 c.638C>T p.A213V Substitution - Missense 10:92349755-92349755 + HCT15 COSM1675429 c.146G>A p.R49H Substitution - Missense 10:92311245-92311245 + TCGA-C4-A0EZ-01 COSM415414 c.670G>A p.G224S Substitution - Missense 10:92349787-92349787 + CHC892T COSM4960816 c.92G>A p.R31K Substitution - Missense 10:92311191-92311191 + DLD1 COSM1675429 c.146G>A p.R49H Substitution - Missense 10:92311245-92311245 + RK119_C01 COSM3738781 c.623G>A p.R208Q Substitution - Missense 10:92349740-92349740 + ESCC-D20 COSM5045943 c.403_404delGA p.R136fs*2 Deletion - Frameshift 10:92349382-92349383 + LIM2405 COSM428132 c.508C>T p.R170C Substitution - Missense 10:92349487-92349487 + 587376 COSM1214562 c.731C>T p.A244V Substitution - Missense 10:92351101-92351101 + 01-P459 COSM4573888 c.120A>G p.K40K Substitution - coding silent 10:92311219-92311219 + TCGA-CG-5721-01 COSM4016621 c.76A>C p.T26P Substitution - Missense 10:92311175-92311175 + T578 COSM4700690 c.37A>C p.S13R Substitution - Missense 10:92311136-92311136 + S02093 COSM5673055 c.14C>A p.A5D Substitution - Missense 10:92291508-92291508 + ESCC_16 COSM5625732 c.782A>G p.Y261C Substitution - Missense 10:92351152-92351152 + RK119_C01 COSM3738780 c.252C>T p.Y84Y Substitution - coding silent 10:92340686-92340686 + TCGA-E2-A1AZ-01 COSM428133 c.800G>A p.R267H Substitution - Missense 10:92351170-92351170 + TCGA-D1-A17Q-01 COSM921460 c.719T>C p.L240S Substitution - Missense 10:92349836-92349836 + HCT8 COSM1675429 c.146G>A p.R49H Substitution - Missense 10:92311245-92311245 + CP66-MEL COSM23470 c.604G>A p.D202N Substitution - Missense 10:92349721-92349721 + HCC2998 COSM1675428 c.36A>C p.R12S Substitution - Missense 10:92311135-92311135 + S02348 COSM5694429 c.403G>T p.E135* Substitution - Nonsense 10:92349382-92349382 + CT-TC COSM4989369 c.637G>A p.A213T Substitution - Missense 10:92349754-92349754 + HCC139T COSM1603854 c.231A>G p.P77P Substitution - coding silent 10:92311330-92311330 + HCC88T COSM1603855 c.262C>G p.L88V Substitution - Missense 10:92340696-92340696 + TCGA-JX-A3Q0-01 COSM4824508 c.90G>A p.V30V Substitution - coding silent 10:92311189-92311189 + C0021T COSM4165571 c.319G>A p.G107S Substitution - Missense 10:92340753-92340753 + T3091 COSM4700691 c.836delA p.*279fs? Deletion - Frameshift 10:92351206-92351206 + TCGA-D8-A1JA-01 COSM3807987 c.64G>A p.E22K Substitution - Missense 10:92311163-92311163 + UM-SCC-2 COSM23470 c.604G>A p.D202N Substitution - Missense 10:92349721-92349721 + HCC139 COSM1603854 c.231A>G p.P77P Substitution - coding silent 10:92311330-92311330 + CHEWS008 COSM3738780 c.252C>T p.Y84Y Substitution - coding silent 10:92340686-92340686 + BD124T COSM5492676 c.253G>A p.V85I Substitution - Missense 10:92340687-92340687 + TCGA-FW-A3R5-06 COSM3868049 c.645C>T p.V215V Substitution - coding silent 10:92349762-92349762 + S02256 COSM5681196 c.205A>T p.N69Y Substitution - Missense 10:92311304-92311304 + PT46 COSM5929198 c.415C>T p.P139S Substitution - Missense 10:92349394-92349394 + TCGA-AP-A051-01 COSM921457 c.390T>A p.G130G Substitution - coding silent 10:92349369-92349369 + HCT-15 COSM1675429 c.146G>A p.R49H Substitution - Missense 10:92311245-92311245 + 8066479 COSM1969573 c.268G>C p.D90H Substitution - Missense 10:92340702-92340702 + TCGA-D8-A1JA-01 COSM3807988 c.70G>C p.D24H Substitution - Missense 10:92311169-92311169 + NCHP_DIPG111 COSM4746182 c.664A>G p.I222V Substitution - Missense 10:92349781-92349781 + TCGA-EE-A29M-06 COSM3441525 c.575G>A p.R192Q Substitution - Missense 10:92349692-92349692 + Gp2D COSM1969577 c.638C>T p.A213V Substitution - Missense 10:92349755-92349755 + TCGA-B0-5692-01 COSM466087 c.609T>G p.H203Q Substitution - Missense 10:92349726-92349726 + SMS-CTR COSM4989369 c.637G>A p.A213T Substitution - Missense 10:92349754-92349754 + TCGA-A8-A09Q-01 COSM428132 c.508C>T p.R170C Substitution - Missense 10:92349487-92349487 + TCGA-BR-4370-01 COSM4016623 c.563G>T p.C188F Substitution - Missense 10:92349680-92349680 + TCGA-D8-A1JA-01 COSM3807989 c.185G>C p.R62T Substitution - Missense 10:92311284-92311284 + PT44 COSM5926742 c.229C>T p.P77S Substitution - Missense 10:92311328-92311328 + TCGA-CD-A486-01 COSM4016622 c.333G>A p.W111* Substitution - Nonsense 10:92340767-92340767 + SJRHB012 COSM4776361 c.479G>A p.R160H Substitution - Missense 10:92349458-92349458 + TCGA-D1-A0ZO-01 COSM921459 c.688A>T p.S230C Substitution - Missense 10:92349805-92349805 + TCGA-66-2795-01 COSM686085 c.574C>A p.R192R Substitution - coding silent 10:92349691-92349691 + HCC2998 COSM1675428 c.36A>C p.R12S Substitution - Missense 10:92311135-92311135 + CHC892T COSM4960816 c.92G>A p.R31K Substitution - Missense 10:92311191-92311191 + ESCC_124 COSM5640970 c.333G>T p.W111C Substitution - Missense 10:92340767-92340767 + TCGA-B5-A11E-01 COSM921458 c.622C>T p.R208* Substitution - Nonsense 10:92349739-92349739 + ESCC_61 COSM5632848 c.709A>G p.R237G Substitution - Missense 10:92349826-92349826 + TCGA-D8-A1Y1-01 COSM428132 c.508C>T p.R170C Substitution - Missense 10:92349487-92349487 + TCGA-F4-6856-01 COSM1349807 c.42C>T p.C14C Substitution - coding silent 10:92311141-92311141 + TCGA-CZ-5463-01 COSM466088 c.822A>T p.E274D Substitution - Missense 10:92351192-92351192 + HCC88 COSM1603855 c.262C>G p.L88V Substitution - Missense 10:92340696-92340696 + TCGA-D1-A167-01 COSM921456 c.194G>A p.C65Y Substitution - Missense 10:92311293-92311293 + TCGA-D1-A16X-01 COSM921455 c.127C>A p.H43N Substitution - Missense 10:92311226-92311226 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.573423;Hs.573426;Hs.573436;Hs.573437;Hs.573440;Hs.573442;Hs.573446;Hs.573448;Hs.573449;Hs.573465;Hs.573466;Hs.573472;Hs.573478;Hs.573484;Hs.573487;Hs.573490 10q23.32-q23.33 610637 2453396|CGAP|BC015480|C/G|non-coding||2310|Validated

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G IntronicSNV . c.239-22A>G 10 94100408 CLL A T Missense p.E274D c.822A>T 10 94110949 RCCC A T Missense p.S230C c.688A>T 10 94109562 UCEC C A Synonymous p.R192R c.574C>A 10 94109448 LUSC C T Missense p.R170C c.508C>T 10 94109244 BRCA G A Missense p.G224S c.670G>A 10 94109544 BLCA G A Missense p.R192Q c.575G>A 10 94109449 CM G A Missense p.R267H c.800G>A 10 94110927 BRCA G T Missense p.C188F c.563G>T 10 94109437 STAD TA - IntronicDeletion . c.35+3874_35+3875delAT 10 94055159 CLL T G Missense p.H203Q c.609T>G 10 94109483 RCCC