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 11 65729273 65729273 + Missense_Mutation SNP C C G TCGA-BL-A13I-01A-11D-A13W-08 TCGA-BL-A13I-11A-11D-A13W-08 g.chr11:65729273C>G c.22C>G c.(22-24)Cgc>Ggc p.R8G BLCA 11 65729273 65729273 + Missense_Mutation SNP C C T TCGA-LT-A5Z6-01A-11D-A289-08 TCGA-LT-A5Z6-10A-01D-A289-08 g.chr11:65729273C>T c.22C>T c.(22-24)Cgc>Tgc p.R8C BLCA 11 65732636 65732636 + Silent SNP G G C TCGA-XF-A9SG-01A-12D-A42E-08 TCGA-XF-A9SG-10A-01D-A42H-08 g.chr11:65732636G>C c.501G>C c.(499-501)ctG>ctC p.L167L BLCA 11 65733594 65733594 + Missense_Mutation SNP G G C TCGA-XF-A9SG-01A-12D-A42E-08 TCGA-XF-A9SG-10A-01D-A42H-08 g.chr11:65733594G>C c.886G>C c.(886-888)Gat>Cat p.D296H BLCA 11 65734819 65734819 + Silent SNP C C T TCGA-DK-AA71-01A-31D-A391-08 TCGA-DK-AA71-10A-01D-A394-08 g.chr11:65734819C>T c.1278C>T c.(1276-1278)ctC>ctT p.L426L BRCA 11 65744012 65744012 + Silent SNP C C T TCGA-A2-A1FW-01A-11D-A13L-09 TCGA-A2-A1FW-10A-01D-A13O-09 g.chr11:65744012C>T c.1719C>T c.(1717-1719)ggC>ggT p.G573G BRCA 11 65744186 65744186 + Silent SNP G G A TCGA-GM-A2DO-01A-11D-A19Y-09 TCGA-GM-A2DO-10D-01D-A18P-09 g.chr11:65744186G>A c.1806G>A c.(1804-1806)gaG>gaA p.E602E BRCA 11 65745270 65745270 + Missense_Mutation SNP A A G TCGA-OL-A5S0-01A-11D-A28B-09 TCGA-OL-A5S0-10A-01D-A28E-09 g.chr11:65745270A>G c.2072A>G c.(2071-2073)tAc>tGc p.Y691C BRCA 11 65745368 65745368 + Nonsense_Mutation SNP G G T TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr11:65745368G>T c.2170G>T c.(2170-2172)Gag>Tag p.E724* BRCA 11 65746121 65746121 + Missense_Mutation SNP G G T TCGA-E2-A1IH-01A-11D-A188-09 TCGA-E2-A1IH-10A-01D-A13O-09 g.chr11:65746121G>T c.2223G>T c.(2221-2223)atG>atT p.M741I BRCA 11 65746162 65746162 + Splice_Site DEL T T - TCGA-BH-A0HX-01A-21W-A071-09 TCGA-BH-A0HX-10A-02W-A071-09 g.chr11:65746162delT c.e18+2 CESC 11 65733421 65733421 + Missense_Mutation SNP G G A TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr11:65733421G>A c.802G>A c.(802-804)Gaa>Aaa p.E268K CESC 11 65735054 65735054 + Missense_Mutation SNP G G C TCGA-JW-A5VL-01A-11D-A28B-09 TCGA-JW-A5VL-10A-01D-A28E-09 g.chr11:65735054G>C c.1426G>C c.(1426-1428)Gag>Cag p.E476Q COAD 11 65745072 65745073 + Frame_Shift_Del DEL AA AA - TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr11:65745072_65745073delAA c.1984_1985delAA c.(1984-1986)aagfs p.K662fs COAD 11 65745241 65745241 + Silent SNP C C A TCGA-G4-6310-01A-11D-1719-10 TCGA-G4-6310-10A-01D-1720-10 g.chr11:65745241C>A c.2043C>A c.(2041-2043)atC>atA p.I681I COADREAD 11 65745072 65745073 + Frame_Shift_Del DEL AA AA - TCGA-AA-A00J-01A-02W-A005-10 TCGA-AA-A00J-10A-01W-A005-10 g.chr11:65745072_65745073delAA c.1984_1985delAA c.(1984-1986)aagfs p.K662fs COADREAD 11 65745241 65745241 + Silent SNP C C A TCGA-G4-6310-01A-11D-1719-10 TCGA-G4-6310-10A-01D-1720-10 g.chr11:65745241C>A c.2043C>A c.(2041-2043)atC>atA p.I681I ESCA 11 65733370 65733370 + Missense_Mutation SNP G G T TCGA-IG-A4P3-01A-11D-A27G-09 TCGA-IG-A4P3-10A-01D-A27G-09 g.chr11:65733370G>T c.751G>T c.(751-753)Gcc>Tcc p.A251S GBM 11 65743897 65743897 + Missense_Mutation SNP G G A TCGA-14-1823-01A-01W-0643-08 TCGA-14-1823-10A-01W-0644-08 g.chr11:65743897G>A c.1604G>A c.(1603-1605)cGc>cAc p.R535H GBMLGG 11 65729299 65729299 + Silent SNP G G T TCGA-E1-A7YS-01A-11D-A34A-08 TCGA-E1-A7YS-10A-01D-A34A-08 g.chr11:65729299G>T c.48G>T c.(46-48)acG>acT p.T16T GBMLGG 11 65733943 65733943 + Silent SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:65733943C>A c.1104C>A c.(1102-1104)atC>atA p.I368I GBMLGG 11 65733982 65733982 + Silent SNP A A G TCGA-DB-5279-01A-01D-1468-08 TCGA-DB-5279-10A-01D-1468-08 g.chr11:65733982A>G c.1143A>G c.(1141-1143)acA>acG p.T381T GBMLGG 11 65734851 65734851 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:65734851C>A c.1310C>A c.(1309-1311)tCc>tAc p.S437Y GBMLGG 11 65743897 65743897 + Missense_Mutation SNP G G A TCGA-14-1823-01A-01W-0643-08 TCGA-14-1823-10A-01W-0644-08 g.chr11:65743897G>A c.1604G>A c.(1603-1605)cGc>cAc p.R535H GBMLGG 11 65745328 65745328 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:65745328C>T c.2130C>T c.(2128-2130)atC>atT p.I710I HNSC 11 65732031 65732031 + Silent SNP C C T TCGA-CV-7425-01A-11D-2078-08 TCGA-CV-7425-10A-01D-2078-08 g.chr11:65732031C>T c.417C>T c.(415-417)gcC>gcT p.A139A HNSC 11 65734019 65734019 + Missense_Mutation SNP G G C TCGA-MT-A67F-01A-11D-A30E-08 TCGA-MT-A67F-10A-01D-A30H-08 g.chr11:65734019G>C c.1180G>C c.(1180-1182)Gag>Cag p.E394Q HNSC 11 65735028 65735028 + Missense_Mutation SNP G G A TCGA-CV-5976-01A-11D-1683-08 TCGA-CV-5976-11A-01D-1683-08 g.chr11:65735028G>A c.1400G>A c.(1399-1401)cGa>cAa p.R467Q HNSC 11 65744017 65744017 + Missense_Mutation SNP G G A TCGA-CR-7371-01A-11D-2012-08 TCGA-CR-7371-10A-01D-2013-08 g.chr11:65744017G>A c.1724G>A c.(1723-1725)cGc>cAc p.R575H KICH 11 65744159 65744159 + Silent SNP C C T TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr11:65744159C>T c.1779C>T c.(1777-1779)aaC>aaT p.N593N KIPAN 11 65744127 65744127 + Splice_Site SNP G G C TCGA-5P-A9K3-01A-11D-A42J-10 TCGA-5P-A9K3-10A-01D-A42M-10 g.chr11:65744127G>C c.1747G>C c.(1747-1749)Gac>Cac p.D583H KIPAN 11 65744159 65744159 + Silent SNP C C T TCGA-KN-8428-01A-11D-2310-10 TCGA-KN-8428-11A-01D-2311-10 g.chr11:65744159C>T c.1779C>T c.(1777-1779)aaC>aaT p.N593N KIRP 11 65744127 65744127 + Splice_Site SNP G G C TCGA-5P-A9K3-01A-11D-A42J-10 TCGA-5P-A9K3-10A-01D-A42M-10 g.chr11:65744127G>C c.1747G>C c.(1747-1749)Gac>Cac p.D583H LGG 11 65729299 65729299 + Silent SNP G G T TCGA-E1-A7YS-01A-11D-A34A-08 TCGA-E1-A7YS-10A-01D-A34A-08 g.chr11:65729299G>T c.48G>T c.(46-48)acG>acT p.T16T LGG 11 65733943 65733943 + Silent SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:65733943C>A c.1104C>A c.(1102-1104)atC>atA p.I368I LGG 11 65733982 65733982 + Silent SNP A A G TCGA-DB-5279-01A-01D-1468-08 TCGA-DB-5279-10A-01D-1468-08 g.chr11:65733982A>G c.1143A>G c.(1141-1143)acA>acG p.T381T LGG 11 65734851 65734851 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:65734851C>A c.1310C>A c.(1309-1311)tCc>tAc p.S437Y LGG 11 65745328 65745328 + Silent SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr11:65745328C>T c.2130C>T c.(2128-2130)atC>atT p.I710I LIHC 11 65743929 65743929 + Missense_Mutation SNP G G A TCGA-ED-A82E-01A-11D-A34Z-10 TCGA-ED-A82E-10A-01D-A34Z-10 g.chr11:65743929G>A c.1636G>A c.(1636-1638)Gag>Aag p.E546K LIHC 11 65744188 65744188 + Missense_Mutation SNP A A G TCGA-G3-A3CJ-01A-11D-A20W-10 TCGA-G3-A3CJ-10A-01D-A20W-10 g.chr11:65744188A>G c.1808A>G c.(1807-1809)aAc>aGc p.N603S LIHC 11 65745300 65745300 + Missense_Mutation SNP A A G TCGA-BC-A3KF-01A-11D-A20W-10 TCGA-BC-A3KF-10A-01D-A20W-10 g.chr11:65745300A>G c.2102A>G c.(2101-2103)aAg>aGg p.K701R LUAD 11 65732040 65732040 + Splice_Site SNP G G C TCGA-05-4389-01A-01D-1265-08 TCGA-05-4389-10A-01D-1265-08 g.chr11:65732040G>C c.426G>C c.(424-426)aaG>aaC p.K142N LUAD 11 65733831 65733831 + Missense_Mutation SNP G G T TCGA-97-7554-01A-11D-2036-08 TCGA-97-7554-10A-01D-2036-08 g.chr11:65733831G>T c.992G>T c.(991-993)cGc>cTc p.R331L LUAD 11 65733911 65733911 + Missense_Mutation SNP G G A TCGA-95-7947-01A-11D-2184-08 TCGA-95-7947-10A-01D-2184-08 g.chr11:65733911G>A c.1072G>A c.(1072-1074)Gat>Aat p.D358N LUAD 11 65733926 65733926 + Silent SNP C C A TCGA-44-A47A-01A-21D-A24D-08 TCGA-44-A47A-10A-01D-A24F-08 g.chr11:65733926C>A c.1087C>A c.(1087-1089)Cgg>Agg p.R363R LUAD 11 65734948 65734948 + Silent SNP G G T TCGA-MN-A4N4-01A-12D-A24P-08 TCGA-MN-A4N4-10A-01D-A24P-08 g.chr11:65734948G>T c.1320G>T c.(1318-1320)cgG>cgT p.R440R LUAD 11 65743992 65743992 + Missense_Mutation SNP C C G TCGA-91-6828-01A-11D-1855-08 TCGA-91-6828-10A-01D-1855-08 g.chr11:65743992C>G c.1699C>G c.(1699-1701)Ccc>Gcc p.P567A LUAD 11 65745041 65745041 + Silent SNP G G T TCGA-17-Z049-01A-01W-0746-08 TCGA-17-Z049-11A-01W-0747-08 g.chr11:65745041G>T c.1953G>T c.(1951-1953)ctG>ctT p.L651L LUAD 11 65746353 65746353 + Silent SNP C C T TCGA-NJ-A4YP-01A-11D-A25L-08 TCGA-NJ-A4YP-10A-01D-A25L-08 g.chr11:65746353C>T c.2352C>T c.(2350-2352)atC>atT p.I784I LUSC 11 65733956 65733956 + Missense_Mutation SNP C C G TCGA-39-5027-01A-21D-1817-08 TCGA-39-5027-11A-01D-1817-08 g.chr11:65733956C>G c.1117C>G c.(1117-1119)Cgg>Ggg p.R373G LUSC 11 65743954 65743954 + Missense_Mutation SNP A A T TCGA-66-2763-01A-01D-1522-08 TCGA-66-2763-11A-01D-1522-08 g.chr11:65743954A>T c.1661A>T c.(1660-1662)aAc>aTc p.N554I OV 11 65745239 65745239 + Missense_Mutation SNP A A G TCGA-09-1669-01A-01W-0615-10 TCGA-09-1669-10A-01W-0616-10 g.chr11:65745239A>G c.2041A>G c.(2041-2043)Atc>Gtc p.I681V SKCM 11 65729299 65729299 + Silent SNP G G A TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr11:65729299G>A c.48G>A c.(46-48)acG>acA p.T16T SKCM 11 65732612 65732612 + Missense_Mutation SNP G G A TCGA-EE-A181-06A-11D-A196-08 TCGA-EE-A181-10A-01D-A198-08 g.chr11:65732612G>A c.477G>A c.(475-477)atG>atA p.M159I SKCM 11 65733863 65733863 + Missense_Mutation SNP G G A TCGA-EE-A2GE-06A-11D-A196-08 TCGA-EE-A2GE-10A-01D-A198-08 g.chr11:65733863G>A c.1024G>A c.(1024-1026)Gaa>Aaa p.E342K SKCM 11 65734802 65734802 + Missense_Mutation SNP G G A TCGA-D3-A2JL-06A-11D-A196-08 TCGA-D3-A2JL-10A-01D-A198-08 g.chr11:65734802G>A c.1261G>A c.(1261-1263)Gat>Aat p.D421N SKCM 11 65734964 65734964 + Nonsense_Mutation SNP C C T TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr11:65734964C>T c.1336C>T c.(1336-1338)Cga>Tga p.R446*

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation ALL-US 11 65726657 65726657 single base substitution T C upstream_gene_variant BLCA-US 11 65729273 65729273 single base substitution C G exon_variant BLCA-US 11 65729273 65729273 single base substitution C G missense_variant R8G 22C>G BRCA-EU 11 65726355 65726355 single base substitution C T upstream_gene_variant BRCA-EU 11 65726529 65726529 single base substitution G C upstream_gene_variant BRCA-EU 11 65727678 65727678 single base substitution C G upstream_gene_variant BRCA-EU 11 65728226 65728226 single base substitution C G upstream_gene_variant BRCA-EU 11 65729563 65729563 single base substitution C G splice_region_variant BRCA-EU 11 65730975 65730975 single base substitution C G intron_variant BRCA-EU 11 65731385 65731385 single base substitution C A intron_variant BRCA-EU 11 65732168 65732168 single base substitution G A downstream_gene_variant BRCA-EU 11 65732168 65732168 single base substitution G A intron_variant BRCA-EU 11 65733325 65733325 single base substitution G A downstream_gene_variant BRCA-EU 11 65733325 65733325 single base substitution G A intron_variant BRCA-EU 11 65734791 65734791 single base substitution T C downstream_gene_variant BRCA-EU 11 65734791 65734791 single base substitution T C missense_variant V417A 1250T>C BRCA-EU 11 65736272 65736272 single base substitution G A downstream_gene_variant BRCA-EU 11 65736272 65736272 single base substitution G A intron_variant BRCA-EU 11 65736616 65736616 single base substitution T G downstream_gene_variant BRCA-EU 11 65736616 65736616 single base substitution T G intron_variant BRCA-EU 11 65737363 65737363 single base substitution T C downstream_gene_variant BRCA-EU 11 65737363 65737363 single base substitution T C intron_variant BRCA-EU 11 65738081 65738081 single base substitution C A downstream_gene_variant BRCA-EU 11 65738081 65738081 single base substitution C A intron_variant BRCA-EU 11 65741626 65741626 single base substitution G A intron_variant BRCA-EU 11 65741626 65741626 single base substitution G A upstream_gene_variant BRCA-EU 11 65742362 65742362 single base substitution T A intron_variant BRCA-EU 11 65742362 65742362 single base substitution T A upstream_gene_variant BRCA-EU 11 65743112 65743112 single base substitution A T intron_variant BRCA-EU 11 65743112 65743112 single base substitution A T upstream_gene_variant BRCA-EU 11 65744152 65744152 single base substitution C T missense_variant S591L 1772C>T BRCA-EU 11 65744152 65744152 single base substitution C T upstream_gene_variant BRCA-EU 11 65744923 65744923 single base substitution C A intron_variant BRCA-EU 11 65744923 65744923 single base substitution C A upstream_gene_variant BRCA-EU 11 65745012 65745012 single base substitution C G intron_variant BRCA-EU 11 65745012 65745012 single base substitution C G upstream_gene_variant BRCA-EU 11 65746686 65746686 single base substitution G A 3_prime_UTR_variant BRCA-EU 11 65746686 65746686 single base substitution G A downstream_gene_variant BRCA-EU 11 65747844 65747844 single base substitution C T downstream_gene_variant BRCA-EU 11 65748257 65748257 single base substitution G C downstream_gene_variant BRCA-EU 11 65751198 65751198 single base substitution G C downstream_gene_variant BRCA-EU 11 65751900 65751900 single base substitution C G downstream_gene_variant BRCA-FR 11 65732168 65732168 single base substitution G A downstream_gene_variant BRCA-FR 11 65732168 65732168 single base substitution G A intron_variant BRCA-FR 11 65737363 65737363 single base substitution T C downstream_gene_variant BRCA-FR 11 65737363 65737363 single base substitution T C intron_variant BRCA-FR 11 65744152 65744152 single base substitution C T missense_variant S591L 1772C>T BRCA-FR 11 65744152 65744152 single base substitution C T upstream_gene_variant BRCA-FR 11 65746686 65746686 single base substitution G A 3_prime_UTR_variant BRCA-FR 11 65746686 65746686 single base substitution G A downstream_gene_variant BRCA-FR 11 65750453 65750453 single base substitution C T downstream_gene_variant BRCA-FR 11 65750525 65750525 single base substitution C T downstream_gene_variant BRCA-FR 11 65751180 65751180 single base substitution C T downstream_gene_variant BRCA-FR 11 65751401 65751401 single base substitution C T downstream_gene_variant BRCA-FR 11 65751533 65751533 single base substitution C G downstream_gene_variant BRCA-UK 11 65735439 65735439 single base substitution G C downstream_gene_variant BRCA-UK 11 65735439 65735439 single base substitution G C intron_variant BRCA-UK 11 65737720 65737720 single base substitution C G downstream_gene_variant BRCA-UK 11 65737720 65737720 single base substitution C G intron_variant BRCA-UK 11 65745700 65745700 single base substitution C T downstream_gene_variant BRCA-UK 11 65745700 65745700 single base substitution C T intron_variant BRCA-UK 11 65745700 65745700 single base substitution C T upstream_gene_variant BRCA-UK 11 65752107 65752107 single base substitution G A downstream_gene_variant BRCA-US 11 65744012 65744012 single base substitution C T synonymous_variant G573G 1719C>T BRCA-US 11 65744012 65744012 single base substitution C T upstream_gene_variant BRCA-US 11 65744186 65744186 single base substitution G A synonymous_variant E602E 1806G>A BRCA-US 11 65744186 65744186 single base substitution G A upstream_gene_variant BRCA-US 11 65745270 65745270 single base substitution A G exon_variant BRCA-US 11 65745270 65745270 single base substitution A G missense_variant Y691C 2072A>G BRCA-US 11 65745270 65745270 single base substitution A G upstream_gene_variant BRCA-US 11 65745368 65745368 single base substitution G T exon_variant BRCA-US 11 65745368 65745368 single base substitution G T splice_region_variant BRCA-US 11 65745368 65745368 single base substitution G T stop_gained E724* 2170G>T BRCA-US 11 65745368 65745368 single base substitution G T upstream_gene_variant BRCA-US 11 65746121 65746121 single base substitution G T downstream_gene_variant BRCA-US 11 65746121 65746121 single base substitution G T exon_variant BRCA-US 11 65746121 65746121 single base substitution G T missense_variant M741I 2223G>T BRCA-US 11 65746162 65746162 deletion of <=200bp T - downstream_gene_variant BRCA-US 11 65746162 65746162 deletion of <=200bp T - splice_donor_variant BTCA-JP 11 65726358 65726358 single base substitution C A upstream_gene_variant BTCA-JP 11 65734764 65734764 single base substitution A T downstream_gene_variant BTCA-JP 11 65734764 65734764 single base substitution A T exon_variant BTCA-JP 11 65734764 65734764 single base substitution A T missense_variant K408I 1223A>T BTCA-JP 11 65743932 65743932 single base substitution C T missense_variant R547W 1639C>T BTCA-JP 11 65743932 65743932 single base substitution C T upstream_gene_variant BTCA-JP 11 65745328 65745328 single base substitution C T exon_variant BTCA-JP 11 65745328 65745328 single base substitution C T synonymous_variant I710I 2130C>T BTCA-JP 11 65745328 65745328 single base substitution C T upstream_gene_variant CESC-US 11 65733421 65733421 single base substitution G A downstream_gene_variant CESC-US 11 65733421 65733421 single base substitution G A exon_variant CESC-US 11 65733421 65733421 single base substitution G A missense_variant E268K 802G>A CESC-US 11 65735054 65735054 single base substitution G C downstream_gene_variant CESC-US 11 65735054 65735054 single base substitution G C missense_variant E476Q 1426G>C CLLE-ES 11 65738647 65738647 single base substitution G T downstream_gene_variant CLLE-ES 11 65738647 65738647 single base substitution G T intron_variant COAD-US 11 65732651 65732651 single base substitution G A 3_prime_UTR_variant COAD-US 11 65732651 65732651 single base substitution G A downstream_gene_variant COAD-US 11 65732651 65732651 single base substitution G A exon_variant COAD-US 11 65732651 65732651 single base substitution G A synonymous_variant A172A 516G>A COAD-US 11 65746353 65746353 single base substitution C T downstream_gene_variant COAD-US 11 65746353 65746353 single base substitution C T exon_variant COAD-US 11 65746353 65746353 single base substitution C T synonymous_variant I784I 2352C>T COCA-CN 11 65726162 65726162 single base substitution G A upstream_gene_variant COCA-CN 11 65727315 65727315 single base substitution G A upstream_gene_variant COCA-CN 11 65727354 65727354 single base substitution C T upstream_gene_variant COCA-CN 11 65742933 65742933 single base substitution T C intron_variant COCA-CN 11 65742933 65742933 single base substitution T C upstream_gene_variant COCA-CN 11 65743142 65743142 single base substitution A T intron_variant COCA-CN 11 65743142 65743142 single base substitution A T upstream_gene_variant COCA-CN 11 65743929 65743929 single base substitution G A missense_variant E546K 1636G>A COCA-CN 11 65743929 65743929 single base substitution G A upstream_gene_variant COCA-CN 11 65744275 65744275 single base substitution T C intron_variant COCA-CN 11 65744275 65744275 single base substitution T C upstream_gene_variant COCA-CN 11 65744303 65744303 single base substitution C T intron_variant COCA-CN 11 65744303 65744303 single base substitution C T upstream_gene_variant COCA-CN 11 65745208 65745208 single base substitution A G intron_variant COCA-CN 11 65745208 65745208 single base substitution A G upstream_gene_variant ESAD-UK 11 65724229 65724229 single base substitution A T upstream_gene_variant ESAD-UK 11 65725247 65725247 single base substitution C T upstream_gene_variant ESAD-UK 11 65727555 65727555 single base substitution T C upstream_gene_variant ESAD-UK 11 65727902 65727902 single base substitution C G upstream_gene_variant ESAD-UK 11 65728639 65728639 single base substitution C T upstream_gene_variant ESAD-UK 11 65733042 65733042 single base substitution C T downstream_gene_variant ESAD-UK 11 65733042 65733042 single base substitution C T intron_variant ESAD-UK 11 65737618 65737618 single base substitution T G downstream_gene_variant ESAD-UK 11 65737618 65737618 single base substitution T G intron_variant ESAD-UK 11 65739283 65739283 single base substitution G T downstream_gene_variant ESAD-UK 11 65739283 65739283 single base substitution G T intron_variant ESAD-UK 11 65739283 65739283 single base substitution G T upstream_gene_variant ESAD-UK 11 65744304 65744304 single base substitution G A intron_variant ESAD-UK 11 65744304 65744304 single base substitution G A upstream_gene_variant ESAD-UK 11 65745089 65745089 single base substitution G A exon_variant ESAD-UK 11 65745089 65745089 single base substitution G A synonymous_variant S667S 2001G>A ESAD-UK 11 65745089 65745089 single base substitution G A upstream_gene_variant ESAD-UK 11 65745434 65745434 single base substitution G A exon_variant ESAD-UK 11 65745434 65745434 single base substitution G A intron_variant ESAD-UK 11 65745434 65745434 single base substitution G A upstream_gene_variant ESAD-UK 11 65747157 65747157 single base substitution A T 3_prime_UTR_variant ESAD-UK 11 65747157 65747157 single base substitution A T downstream_gene_variant ESAD-UK 11 65747271 65747271 single base substitution T G 3_prime_UTR_variant ESAD-UK 11 65747271 65747271 single base substitution T G downstream_gene_variant ESAD-UK 11 65748485 65748485 single base substitution C T downstream_gene_variant ESAD-UK 11 65749510 65749510 single base substitution C T downstream_gene_variant ESAD-UK 11 65750011 65750011 single base substitution G T downstream_gene_variant ESAD-UK 11 65751484 65751484 single base substitution C T downstream_gene_variant ESAD-UK 11 65752046 65752046 single base substitution A G downstream_gene_variant ESAD-UK 11 65752175 65752175 single base substitution G C downstream_gene_variant ESCA-CN 11 65746200 65746200 single base substitution G A downstream_gene_variant ESCA-CN 11 65746200 65746200 single base substitution G A intron_variant GBM-US 11 65743897 65743897 single base substitution G A missense_variant R535H 1604G>A GBM-US 11 65743897 65743897 single base substitution G A upstream_gene_variant LAML-KR 11 65727339 65727339 single base substitution A G upstream_gene_variant LAML-KR 11 65738248 65738248 single base substitution A G downstream_gene_variant LAML-KR 11 65738248 65738248 single base substitution A G intron_variant LAML-KR 11 65738676 65738676 single base substitution T G downstream_gene_variant LAML-KR 11 65738676 65738676 single base substitution T G intron_variant LAML-KR 11 65738790 65738790 single base substitution G A downstream_gene_variant LAML-KR 11 65738790 65738790 single base substitution G A intron_variant LICA-CN 11 65733688 65733688 single base substitution A T downstream_gene_variant LICA-CN 11 65733688 65733688 single base substitution A T exon_variant LICA-CN 11 65733688 65733688 single base substitution A T missense_variant Q327L 980A>T LICA-FR 11 65732876 65732876 single base substitution G T 3_prime_UTR_variant LICA-FR 11 65732876 65732876 single base substitution G T downstream_gene_variant LICA-FR 11 65732876 65732876 single base substitution G T exon_variant LICA-FR 11 65732876 65732876 single base substitution G T missense_variant R206S 618G>T LICA-FR 11 65738316 65738316 single base substitution T G downstream_gene_variant LICA-FR 11 65738316 65738316 single base substitution T G intron_variant LICA-FR 11 65738359 65738359 single base substitution G A downstream_gene_variant LICA-FR 11 65738359 65738359 single base substitution G A intron_variant LICA-FR 11 65739619 65739619 single base substitution T C downstream_gene_variant LICA-FR 11 65739619 65739619 single base substitution T C intron_variant LICA-FR 11 65739619 65739619 single base substitution T C upstream_gene_variant LICA-FR 11 65750326 65750328 deletion of <=200bp AAA - downstream_gene_variant LIHC-US 11 65743929 65743929 single base substitution G A missense_variant E546K 1636G>A LIHC-US 11 65743929 65743929 single base substitution G A upstream_gene_variant LINC-JP 11 65729180 65729180 single base substitution G T 5_prime_UTR_variant LINC-JP 11 65729180 65729180 single base substitution G T upstream_gene_variant LINC-JP 11 65730877 65730877 single base substitution G A intron_variant LINC-JP 11 65731536 65731536 single base substitution T A exon_variant LINC-JP 11 65731536 65731536 single base substitution T A intron_variant LINC-JP 11 65732559 65732559 single base substitution C G downstream_gene_variant LINC-JP 11 65732559 65732559 single base substitution C G exon_variant LINC-JP 11 65732559 65732559 single base substitution C G intron_variant LINC-JP 11 65732559 65732559 single base substitution C G splice_region_variant LIRI-JP 11 65730436 65730436 single base substitution G A intron_variant LIRI-JP 11 65730603 65730603 single base substitution G A intron_variant LIRI-JP 11 65731746 65731746 single base substitution T C exon_variant LIRI-JP 11 65731746 65731746 single base substitution T C intron_variant LIRI-JP 11 65732879 65732879 single base substitution C G 3_prime_UTR_variant LIRI-JP 11 65732879 65732879 single base substitution C G downstream_gene_variant LIRI-JP 11 65732879 65732879 single base substitution C G exon_variant LIRI-JP 11 65732879 65732879 single base substitution C G missense_variant S207R 621C>G LIRI-JP 11 65733549 65733549 single base substitution G T downstream_gene_variant LIRI-JP 11 65733549 65733549 single base substitution G T missense_variant V281L 841G>T LIRI-JP 11 65733549 65733549 single base substitution G T splice_region_variant LIRI-JP 11 65737444 65737444 single base substitution C T downstream_gene_variant LIRI-JP 11 65737444 65737444 single base substitution C T intron_variant LIRI-JP 11 65737695 65737695 single base substitution G T downstream_gene_variant LIRI-JP 11 65737695 65737695 single base substitution G T intron_variant LIRI-JP 11 65740209 65740209 single base substitution A G intron_variant LIRI-JP 11 65740209 65740209 single base substitution A G upstream_gene_variant LIRI-JP 11 65742297 65742297 single base substitution G T intron_variant LIRI-JP 11 65742297 65742297 single base substitution G T upstream_gene_variant LIRI-JP 11 65751609 65751609 single base substitution G A downstream_gene_variant LUSC-KR 11 65724625 65724625 single base substitution C A upstream_gene_variant LUSC-KR 11 65726773 65726773 single base substitution C A upstream_gene_variant LUSC-KR 11 65734701 65734701 single base substitution G T downstream_gene_variant LUSC-KR 11 65734701 65734701 single base substitution G T intron_variant LUSC-KR 11 65736951 65736951 single base substitution C T downstream_gene_variant LUSC-KR 11 65736951 65736951 single base substitution C T intron_variant LUSC-KR 11 65738377 65738377 single base substitution G T downstream_gene_variant LUSC-KR 11 65738377 65738377 single base substitution G T intron_variant LUSC-KR 11 65738766 65738766 single base substitution T G downstream_gene_variant LUSC-KR 11 65738766 65738766 single base substitution T G intron_variant LUSC-KR 11 65738817 65738817 single base substitution A G downstream_gene_variant LUSC-KR 11 65738817 65738817 single base substitution A G intron_variant LUSC-KR 11 65738830 65738830 single base substitution T G downstream_gene_variant LUSC-KR 11 65738830 65738830 single base substitution T G intron_variant LUSC-KR 11 65738846 65738846 single base substitution A G downstream_gene_variant LUSC-KR 11 65738846 65738846 single base substitution A G intron_variant LUSC-KR 11 65738878 65738878 single base substitution A G downstream_gene_variant LUSC-KR 11 65738878 65738878 single base substitution A G intron_variant LUSC-KR 11 65738891 65738891 single base substitution T G downstream_gene_variant LUSC-KR 11 65738891 65738891 single base substitution T G intron_variant LUSC-KR 11 65738923 65738923 single base substitution T G downstream_gene_variant LUSC-KR 11 65738923 65738923 single base substitution T G intron_variant LUSC-KR 11 65739013 65739013 single base substitution T G downstream_gene_variant LUSC-KR 11 65739013 65739013 single base substitution T G intron_variant LUSC-KR 11 65741971 65741971 single base substitution G A intron_variant LUSC-KR 11 65741971 65741971 single base substitution G A upstream_gene_variant LUSC-KR 11 65745931 65745931 single base substitution T C downstream_gene_variant LUSC-KR 11 65745931 65745931 single base substitution T C intron_variant LUSC-KR 11 65745931 65745931 single base substitution T C upstream_gene_variant LUSC-KR 11 65746653 65746653 single base substitution A G 3_prime_UTR_variant LUSC-KR 11 65746653 65746653 single base substitution A G downstream_gene_variant LUSC-KR 11 65748569 65748569 single base substitution G A downstream_gene_variant LUSC-US 11 65733956 65733956 single base substitution C G downstream_gene_variant LUSC-US 11 65733956 65733956 single base substitution C G exon_variant LUSC-US 11 65733956 65733956 single base substitution C G missense_variant R373G 1117C>G LUSC-US 11 65743954 65743954 single base substitution A T missense_variant N554I 1661A>T LUSC-US 11 65743954 65743954 single base substitution A T upstream_gene_variant MALY-DE 11 65724705 65724705 single base substitution T C upstream_gene_variant MALY-DE 11 65741544 65741544 single base substitution A G intron_variant MALY-DE 11 65741544 65741544 single base substitution A G upstream_gene_variant MALY-DE 11 65743669 65743669 single base substitution T C intron_variant MALY-DE 11 65743669 65743669 single base substitution T C upstream_gene_variant MELA-AU 11 65725094 65725094 single base substitution C T upstream_gene_variant MELA-AU 11 65725334 65725334 single base substitution G A upstream_gene_variant MELA-AU 11 65725758 65725758 single base substitution A G upstream_gene_variant MELA-AU 11 65726204 65726204 single base substitution G A upstream_gene_variant MELA-AU 11 65726318 65726318 single base substitution C T upstream_gene_variant MELA-AU 11 65726345 65726345 single base substitution C A upstream_gene_variant MELA-AU 11 65727011 65727011 single base substitution G A upstream_gene_variant MELA-AU 11 65727323 65727323 single base substitution C T upstream_gene_variant MELA-AU 11 65727334 65727334 deletion of <=200bp C - upstream_gene_variant MELA-AU 11 65727550 65727550 single base substitution G A upstream_gene_variant MELA-AU 11 65728996 65728996 single base substitution C T upstream_gene_variant MELA-AU 11 65729127 65729127 single base substitution G A upstream_gene_variant MELA-AU 11 65730864 65730864 single base substitution C T intron_variant MELA-AU 11 65731193 65731193 single base substitution C T intron_variant MELA-AU 11 65731304 65731304 single base substitution A G intron_variant MELA-AU 11 65731379 65731379 single base substitution G A intron_variant MELA-AU 11 65732177 65732177 single base substitution C T downstream_gene_variant MELA-AU 11 65732177 65732177 single base substitution C T intron_variant MELA-AU 11 65732462 65732462 single base substitution C T downstream_gene_variant MELA-AU 11 65732462 65732462 single base substitution C T intron_variant MELA-AU 11 65732559 65732559 single base substitution C T downstream_gene_variant MELA-AU 11 65732559 65732559 single base substitution C T exon_variant MELA-AU 11 65732559 65732559 single base substitution C T intron_variant MELA-AU 11 65732559 65732559 single base substitution C T splice_region_variant MELA-AU 11 65732741 65732741 single base substitution C T downstream_gene_variant MELA-AU 11 65732741 65732741 single base substitution C T intron_variant MELA-AU 11 65732742 65732742 single base substitution C A downstream_gene_variant MELA-AU 11 65732742 65732742 single base substitution C A intron_variant MELA-AU 11 65733739 65733739 single base substitution G A downstream_gene_variant MELA-AU 11 65733739 65733739 single base substitution G A exon_variant MELA-AU 11 65733739 65733739 single base substitution G A intron_variant MELA-AU 11 65734068 65734068 single base substitution C T downstream_gene_variant MELA-AU 11 65734068 65734068 single base substitution C T intron_variant MELA-AU 11 65734327 65734327 single base substitution C T downstream_gene_variant MELA-AU 11 65734327 65734327 single base substitution C T intron_variant MELA-AU 11 65734556 65734556 single base substitution C T downstream_gene_variant MELA-AU 11 65734556 65734556 single base substitution C T intron_variant MELA-AU 11 65735676 65735677 multiple base substitution (>=2bp and <=200bp) CC AT downstream_gene_variant MELA-AU 11 65735676 65735677 multiple base substitution (>=2bp and <=200bp) CC AT intron_variant MELA-AU 11 65735766 65735766 single base substitution C T downstream_gene_variant MELA-AU 11 65735766 65735766 single base substitution C T intron_variant MELA-AU 11 65735773 65735773 single base substitution A G downstream_gene_variant MELA-AU 11 65735773 65735773 single base substitution A G intron_variant MELA-AU 11 65735786 65735786 single base substitution C T downstream_gene_variant MELA-AU 11 65735786 65735786 single base substitution C T intron_variant MELA-AU 11 65738247 65738247 single base substitution G A downstream_gene_variant MELA-AU 11 65738247 65738247 single base substitution G A intron_variant MELA-AU 11 65739891 65739891 single base substitution A G intron_variant MELA-AU 11 65739891 65739891 single base substitution A G upstream_gene_variant MELA-AU 11 65740023 65740024 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 65740023 65740024 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 11 65742157 65742157 single base substitution G A intron_variant MELA-AU 11 65742157 65742157 single base substitution G A upstream_gene_variant MELA-AU 11 65742343 65742343 single base substitution G A intron_variant MELA-AU 11 65742343 65742343 single base substitution G A upstream_gene_variant MELA-AU 11 65742828 65742829 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 11 65742828 65742829 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 11 65743336 65743336 single base substitution C T intron_variant MELA-AU 11 65743336 65743336 single base substitution C T upstream_gene_variant MELA-AU 11 65744557 65744557 single base substitution C T exon_variant MELA-AU 11 65744557 65744557 single base substitution C T synonymous_variant L644L 1930C>T MELA-AU 11 65744557 65744557 single base substitution C T upstream_gene_variant MELA-AU 11 65745427 65745443 deletion of <=200bp GGGCCATGCAATGCCCC - exon_variant MELA-AU 11 65745427 65745443 deletion of <=200bp GGGCCATGCAATGCCCC - intron_variant MELA-AU 11 65745427 65745443 deletion of <=200bp GGGCCATGCAATGCCCC - upstream_gene_variant MELA-AU 11 65746745 65746745 single base substitution C T 3_prime_UTR_variant MELA-AU 11 65746745 65746745 single base substitution C T downstream_gene_variant MELA-AU 11 65747258 65747259 multiple base substitution (>=2bp and <=200bp) CC TT 3_prime_UTR_variant MELA-AU 11 65747258 65747259 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 11 65747292 65747292 single base substitution A C 3_prime_UTR_variant MELA-AU 11 65747292 65747292 single base substitution A C downstream_gene_variant MELA-AU 11 65747405 65747405 single base substitution A G downstream_gene_variant MELA-AU 11 65750390 65750390 single base substitution C T downstream_gene_variant MELA-AU 11 65750433 65750433 single base substitution C T downstream_gene_variant MELA-AU 11 65750868 65750868 single base substitution C T downstream_gene_variant MELA-AU 11 65750917 65750917 single base substitution G A downstream_gene_variant MELA-AU 11 65751267 65751267 single base substitution C T downstream_gene_variant MELA-AU 11 65751489 65751489 single base substitution G A downstream_gene_variant MELA-AU 11 65752265 65752265 single base substitution A C downstream_gene_variant ORCA-IN 11 65730426 65730426 single base substitution G C intron_variant ORCA-IN 11 65735177 65735178 multiple base substitution (>=2bp and <=200bp) CC TA downstream_gene_variant ORCA-IN 11 65735177 65735178 multiple base substitution (>=2bp and <=200bp) CC TA missense_variant S486L 1457CC>TA ORCA-IN 11 65735721 65735721 single base substitution C G downstream_gene_variant ORCA-IN 11 65735721 65735721 single base substitution C G intron_variant ORCA-IN 11 65738253 65738253 deletion of <=200bp A - downstream_gene_variant ORCA-IN 11 65738253 65738253 deletion of <=200bp A - intron_variant ORCA-IN 11 65739797 65739797 single base substitution G A intron_variant ORCA-IN 11 65739797 65739797 single base substitution G A upstream_gene_variant OV-AU 11 65726754 65726754 single base substitution G C upstream_gene_variant OV-AU 11 65729865 65729865 single base substitution G C intron_variant OV-AU 11 65746347 65746347 single base substitution C G downstream_gene_variant OV-AU 11 65746347 65746347 single base substitution C G exon_variant OV-AU 11 65746347 65746347 single base substitution C G synonymous_variant P782P 2346C>G OV-AU 11 65748624 65748624 single base substitution T C downstream_gene_variant OV-AU 11 65748658 65748658 single base substitution C G downstream_gene_variant OV-AU 11 65751046 65751046 single base substitution G A downstream_gene_variant PACA-AU 11 65726969 65726969 single base substitution T A upstream_gene_variant PACA-AU 11 65735204 65735204 single base substitution C T downstream_gene_variant PACA-AU 11 65735204 65735204 single base substitution C T missense_variant A495V 1484C>T PACA-AU 11 65739792 65739792 single base substitution C T intron_variant PACA-AU 11 65739792 65739792 single base substitution C T upstream_gene_variant PACA-AU 11 65740840 65740840 insertion of <=200bp - T intron_variant PACA-AU 11 65740840 65740840 insertion of <=200bp - T upstream_gene_variant PACA-AU 11 65742014 65742014 single base substitution G C intron_variant PACA-AU 11 65742014 65742014 single base substitution G C upstream_gene_variant PACA-AU 11 65744075 65744075 single base substitution G A intron_variant PACA-AU 11 65744075 65744075 single base substitution G A upstream_gene_variant PACA-AU 11 65748996 65748996 single base substitution G A downstream_gene_variant PACA-CA 11 65724244 65724244 single base substitution G C upstream_gene_variant PACA-CA 11 65726913 65726913 single base substitution C T upstream_gene_variant PACA-CA 11 65727033 65727033 single base substitution G A upstream_gene_variant PACA-CA 11 65727245 65727245 single base substitution G A upstream_gene_variant PACA-CA 11 65727688 65727688 single base substitution C G upstream_gene_variant PACA-CA 11 65730642 65730642 single base substitution T C intron_variant PACA-CA 11 65731310 65731310 single base substitution G A intron_variant PACA-CA 11 65733081 65733081 single base substitution G A downstream_gene_variant PACA-CA 11 65733081 65733081 single base substitution G A intron_variant PACA-CA 11 65733613 65733617 deletion of <=200bp AAAAT - downstream_gene_variant PACA-CA 11 65733613 65733617 deletion of <=200bp AAAAT - exon_variant PACA-CA 11 65733613 65733617 deletion of <=200bp AAAAT - frameshift_variant KN302 PACA-CA 11 65736304 65736304 single base substitution G A downstream_gene_variant PACA-CA 11 65736304 65736304 single base substitution G A intron_variant PACA-CA 11 65737219 65737219 single base substitution G T downstream_gene_variant PACA-CA 11 65737219 65737219 single base substitution G T intron_variant PACA-CA 11 65738248 65738248 single base substitution A G downstream_gene_variant PACA-CA 11 65738248 65738248 single base substitution A G intron_variant PACA-CA 11 65743337 65743337 single base substitution G A intron_variant PACA-CA 11 65743337 65743337 single base substitution G A upstream_gene_variant PACA-CA 11 65743798 65743798 single base substitution G T intron_variant PACA-CA 11 65743798 65743798 single base substitution G T upstream_gene_variant PACA-CA 11 65744043 65744043 single base substitution C T splice_region_variant PACA-CA 11 65744043 65744043 single base substitution C T upstream_gene_variant PACA-CA 11 65748941 65748941 single base substitution G T downstream_gene_variant PACA-CA 11 65750547 65750547 single base substitution C A downstream_gene_variant PBCA-DE 11 65728677 65728677 insertion of <=200bp - AAAAAC upstream_gene_variant PBCA-DE 11 65735315 65735315 single base substitution T G downstream_gene_variant PBCA-DE 11 65735315 65735315 single base substitution T G intron_variant PBCA-DE 11 65738248 65738248 single base substitution A G downstream_gene_variant PBCA-DE 11 65738248 65738248 single base substitution A G intron_variant PBCA-DE 11 65746357 65746357 single base substitution C A downstream_gene_variant PBCA-DE 11 65746357 65746357 single base substitution C A exon_variant PBCA-DE 11 65746357 65746357 single base substitution C A missense_variant L786I 2356C>A PRAD-CA 11 65736478 65736478 single base substitution G A downstream_gene_variant PRAD-CA 11 65736478 65736478 single base substitution G A intron_variant PRAD-CA 11 65747599 65747599 single base substitution T A downstream_gene_variant PRAD-UK 11 65738903 65738903 single base substitution G T downstream_gene_variant PRAD-UK 11 65738903 65738903 single base substitution G T intron_variant PRAD-UK 11 65739818 65739818 single base substitution G A intron_variant PRAD-UK 11 65739818 65739818 single base substitution G A upstream_gene_variant PRAD-UK 11 65740473 65740473 single base substitution C T intron_variant PRAD-UK 11 65740473 65740473 single base substitution C T upstream_gene_variant PRAD-UK 11 65741995 65741995 single base substitution C A intron_variant PRAD-UK 11 65741995 65741995 single base substitution C A upstream_gene_variant PRAD-UK 11 65748188 65748188 single base substitution A G downstream_gene_variant RECA-EU 11 65725367 65725367 single base substitution A C upstream_gene_variant RECA-EU 11 65726663 65726663 single base substitution C A upstream_gene_variant RECA-EU 11 65731804 65731804 single base substitution G C exon_variant RECA-EU 11 65731804 65731804 single base substitution G C intron_variant SKCA-BR 11 65728479 65728479 single base substitution T C upstream_gene_variant SKCA-BR 11 65728676 65728676 insertion of <=200bp - AAAAAC upstream_gene_variant SKCA-BR 11 65733740 65733740 single base substitution A G downstream_gene_variant SKCA-BR 11 65733740 65733740 single base substitution A G exon_variant SKCA-BR 11 65733740 65733740 single base substitution A G intron_variant SKCA-BR 11 65735934 65735934 single base substitution G A downstream_gene_variant SKCA-BR 11 65735934 65735934 single base substitution G A intron_variant SKCA-BR 11 65742105 65742105 single base substitution G C intron_variant SKCA-BR 11 65742105 65742105 single base substitution G C upstream_gene_variant SKCA-BR 11 65742881 65742881 insertion of <=200bp - AT intron_variant SKCA-BR 11 65742881 65742881 insertion of <=200bp - AT upstream_gene_variant SKCA-BR 11 65744495 65744495 single base substitution C T exon_variant SKCA-BR 11 65744495 65744495 single base substitution C T missense_variant S623F 1868C>T SKCA-BR 11 65744495 65744495 single base substitution C T upstream_gene_variant SKCA-BR 11 65746338 65746338 single base substitution G A downstream_gene_variant SKCA-BR 11 65746338 65746338 single base substitution G A exon_variant SKCA-BR 11 65746338 65746338 single base substitution G A synonymous_variant Q779Q 2337G>A SKCA-BR 11 65746483 65746483 single base substitution G A downstream_gene_variant SKCA-BR 11 65746483 65746483 single base substitution G A splice_region_variant SKCA-BR 11 65747182 65747182 single base substitution G A 3_prime_UTR_variant SKCA-BR 11 65747182 65747182 single base substitution G A downstream_gene_variant SKCA-BR 11 65747343 65747343 single base substitution G A downstream_gene_variant SKCA-BR 11 65747393 65747393 single base substitution G C downstream_gene_variant SKCA-BR 11 65747630 65747630 single base substitution G C downstream_gene_variant SKCA-BR 11 65747724 65747724 single base substitution G T downstream_gene_variant SKCA-BR 11 65748387 65748387 insertion of <=200bp - CA downstream_gene_variant SKCA-BR 11 65749189 65749189 single base substitution T C downstream_gene_variant SKCA-BR 11 65750995 65750996 deletion of <=200bp GC - downstream_gene_variant SKCA-BR 11 65750996 65750996 single base substitution C A downstream_gene_variant SKCA-BR 11 65750997 65750997 single base substitution G A downstream_gene_variant SKCM-US 11 65726390 65726390 single base substitution G A upstream_gene_variant SKCM-US 11 65729299 65729299 single base substitution G A exon_variant SKCM-US 11 65729299 65729299 single base substitution G A synonymous_variant T16T 48G>A SKCM-US 11 65732014 65732014 single base substitution C T downstream_gene_variant SKCM-US 11 65732014 65732014 single base substitution C T exon_variant SKCM-US 11 65732014 65732014 single base substitution C T missense_variant P134S 400C>T SKCM-US 11 65732612 65732612 single base substitution G A 3_prime_UTR_variant SKCM-US 11 65732612 65732612 single base substitution G A downstream_gene_variant SKCM-US 11 65732612 65732612 single base substitution G A exon_variant SKCM-US 11 65732612 65732612 single base substitution G A missense_variant M159I 477G>A SKCM-US 11 65733863 65733863 single base substitution G A downstream_gene_variant SKCM-US 11 65733863 65733863 single base substitution G A exon_variant SKCM-US 11 65733863 65733863 single base substitution G A missense_variant E342K 1024G>A SKCM-US 11 65734802 65734802 single base substitution G A downstream_gene_variant SKCM-US 11 65734802 65734802 single base substitution G A missense_variant D421N 1261G>A SKCM-US 11 65734964 65734964 single base substitution C T downstream_gene_variant SKCM-US 11 65734964 65734964 single base substitution C T stop_gained R446* 1336C>T STAD-US 11 65729303 65729303 single base substitution G A exon_variant STAD-US 11 65729303 65729303 single base substitution G A missense_variant A18T 52G>A STAD-US 11 65732567 65732567 single base substitution G T downstream_gene_variant STAD-US 11 65732567 65732567 single base substitution G T exon_variant STAD-US 11 65732567 65732567 single base substitution G T synonymous_variant A144A 432G>T STAD-US 11 65733549 65733549 single base substitution G A downstream_gene_variant STAD-US 11 65733549 65733549 single base substitution G A missense_variant V281M 841G>A STAD-US 11 65733549 65733549 single base substitution G A splice_region_variant STAD-US 11 65734962 65734962 single base substitution G A downstream_gene_variant STAD-US 11 65734962 65734962 single base substitution G A missense_variant R445H 1334G>A STAD-US 11 65743960 65743960 single base substitution C T missense_variant T556M 1667C>T STAD-US 11 65743960 65743960 single base substitution C T upstream_gene_variant STAD-US 11 65743976 65743976 single base substitution C T synonymous_variant R561R 1683C>T STAD-US 11 65743976 65743976 single base substitution C T upstream_gene_variant STAD-US 11 65745317 65745317 single base substitution G A exon_variant STAD-US 11 65745317 65745317 single base substitution G A missense_variant D707N 2119G>A STAD-US 11 65745317 65745317 single base substitution G A upstream_gene_variant STAD-US 11 65745360 65745360 single base substitution C T exon_variant STAD-US 11 65745360 65745360 single base substitution C T missense_variant T721I 2162C>T STAD-US 11 65745360 65745360 single base substitution C T upstream_gene_variant STAD-US 11 65746365 65746365 single base substitution C A downstream_gene_variant STAD-US 11 65746365 65746365 single base substitution C A exon_variant STAD-US 11 65746365 65746365 single base substitution C A synonymous_variant G788G 2364C>A STAD-US 11 65746378 65746378 single base substitution A G downstream_gene_variant STAD-US 11 65746378 65746378 single base substitution A G exon_variant STAD-US 11 65746378 65746378 single base substitution A G missense_variant M793V 2377A>G THCA-US 11 65731499 65731499 single base substitution C T exon_variant THCA-US 11 65731499 65731499 single base substitution C T intron_variant UCEC-US 11 65726680 65726680 single base substitution T C upstream_gene_variant UCEC-US 11 65726763 65726763 single base substitution G T upstream_gene_variant UCEC-US 11 65731592 65731592 single base substitution G A exon_variant UCEC-US 11 65731592 65731592 single base substitution G A missense_variant E121K 361G>A UCEC-US 11 65733558 65733558 single base substitution G C downstream_gene_variant UCEC-US 11 65733558 65733558 single base substitution G C exon_variant UCEC-US 11 65733558 65733558 single base substitution G C missense_variant E284Q 850G>C UCEC-US 11 65733607 65733607 single base substitution C T downstream_gene_variant UCEC-US 11 65733607 65733607 single base substitution C T exon_variant UCEC-US 11 65733607 65733607 single base substitution C T missense_variant A300V 899C>T UCEC-US 11 65733829 65733829 single base substitution T C downstream_gene_variant UCEC-US 11 65733829 65733829 single base substitution T C exon_variant UCEC-US 11 65733829 65733829 single base substitution T C synonymous_variant P330P 990T>C UCEC-US 11 65734962 65734962 single base substitution G A downstream_gene_variant UCEC-US 11 65734962 65734962 single base substitution G A missense_variant R445H 1334G>A UCEC-US 11 65744203 65744203 single base substitution C T missense_variant T608M 1823C>T UCEC-US 11 65744203 65744203 single base substitution C T upstream_gene_variant UCEC-US 11 65744523 65744523 single base substitution G A exon_variant UCEC-US 11 65744523 65744523 single base substitution G A synonymous_variant P632P 1896G>A UCEC-US 11 65744523 65744523 single base substitution G A upstream_gene_variant UCEC-US 11 65746326 65746326 single base substitution G T downstream_gene_variant UCEC-US 11 65746326 65746326 single base substitution G T exon_variant UCEC-US 11 65746326 65746326 single base substitution G T missense_variant K775N 2325G>T

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand 2149060 COSM3723476 c.1454G>C p.G485A Substitution - Missense 11:65967703-65967703 + TCGA-AP-A051-01 COSM930596 c.2325G>T p.K775N Substitution - Missense 11:65978855-65978855 + 587222 COSM1224683 c.903G>T p.E301D Substitution - Missense 11:65966140-65966140 + CSCC-31-T COSM4557050 c.712G>A p.E238K Substitution - Missense 11:65965753-65965753 + YUMOBER COSM5373295 c.704C>T p.T235I Substitution - Missense 11:65965745-65965745 + TCGA-ED-A82E-01 COSM4941443 c.1636G>A p.E546K Substitution - Missense 11:65976458-65976458 + TCGA-A5-A0VP-01 COSM930590 c.850G>C p.E284Q Substitution - Missense 11:65966087-65966087 + 1N38-VS-1T38 COSM4975098 c.2237G>A p.R746Q Substitution - Missense 11:65978664-65978664 + CHEWS012 COSM4574682 c.2364C>T p.G788G Substitution - coding silent 11:65978894-65978894 + HCA7 COSM4629810 c.2267T>A p.L756Q Substitution - Missense 11:65978797-65978797 + Pat_01_B COSM5839286 c.314C>T p.A105V Substitution - Missense 11:65964074-65964074 + CHC2211T COSM4801122 c.618G>T p.R206S Substitution - Missense 11:65965405-65965405 + TCGA-BS-A0UF-01 COSM930594 c.1823C>T p.T608M Substitution - Missense 11:65976732-65976732 + TCGA-AA-3710-01 COSM5104662 c.1393G>A p.D465N Substitution - Missense 11:65967550-65967550 + Case3a COSM1717504 c.1792T>A p.S598T Substitution - Missense 11:65976701-65976701 + CHC320T COSM3765585 c.1857+10G>A p.? Unknown 11:65976776-65976776 + 587224 COSM1224682 c.895C>T p.R299W Substitution - Missense 11:65966132-65966132 + TCGA-WS-AB45-01 COSM5189586 c.733C>T p.R245W Substitution - Missense 11:65965774-65965774 + HCC7 COSM1605048 c.314-9T>A p.? Unknown 11:65964065-65964065 + Case3b COSM1717504 c.1792T>A p.S598T Substitution - Missense 11:65976701-65976701 + TCGA-CK-4951-01 COSM2166939 c.2384C>T p.A795V Substitution - Missense 11:65978914-65978914 + TCGA-FP-A4BE-01 COSM4035597 c.841G>A p.V281M Substitution - Missense 11:65966078-65966078 + TCGA-EE-A181-06 COSM3451932 c.477G>A p.M159I Substitution - Missense 11:65965141-65965141 + C135 COSM4617188 c.1034G>A p.R345Q Substitution - Missense 11:65966402-65966402 + pfg258T COSM4616428 c.1087C>T p.R363W Substitution - Missense 11:65966455-65966455 + TCGA-AP-A0LM-01 COSM930593 c.1334G>A p.R445H Substitution - Missense 11:65967491-65967491 + TCGA-EB-A5SE-01 COSM3451931 c.400C>T p.P134S Substitution - Missense 11:65964543-65964543 + TCGA-AX-A060-01 COSM930591 c.899C>T p.A300V Substitution - Missense 11:65966136-65966136 + ESO-169 COSM1264879 c.1177C>T p.P393S Substitution - Missense 11:65966545-65966545 + T3446 COSM4723664 c.325delA p.T110fs*23 Deletion - Frameshift 11:65964085-65964085 + TCGA-G4-6628-01 COSM5179962 c.2384+2T>C p.? Unknown 11:65978916-65978916 + TCGA-BS-A0UF-01 COSM930588 c.361G>A p.E121K Substitution - Missense 11:65964121-65964121 + YUPROST COSM1704251 c.1322G>A p.G441E Substitution - Missense 11:65967479-65967479 + TCGA-D5-6531-01 COSM2166937 c.2352C>T p.I784I Substitution - coding silent 11:65978882-65978882 + TCGA-BR-8680-01 COSM4035600 c.2119G>A p.D707N Substitution - Missense 11:65977846-65977846 + 12-P2194 COSM4574681 c.1662C>T p.N554N Substitution - coding silent 11:65976484-65976484 + ESCC_109 COSM4941443 c.1636G>A p.E546K Substitution - Missense 11:65976458-65976458 + pfg092T COSM4756648 c.623G>A p.R208Q Substitution - Missense 11:65965410-65965410 + TCGA-CG-5721-01 COSM4035601 c.2162C>T p.T721I Substitution - Missense 11:65977889-65977889 + TCGA-CG-5721-01 COSM930593 c.1334G>A p.R445H Substitution - Missense 11:65967491-65967491 + HCC41T COSM1605049 c.428-4C>G p.? Unknown 11:65965088-65965088 + PD7307a COSM5789073 c.1772C>T p.S591L Substitution - Missense 11:65976681-65976681 + TCGA-CG-4442-01 COSM4035595 c.52G>A p.A18T Substitution - Missense 11:65961832-65961832 + SNU-C4 COSM3398053 c.1604G>A p.R535H Substitution - Missense 11:65976426-65976426 + HCC7T COSM1605048 c.314-9T>A p.? Unknown 11:65964065-65964065 + CSCC-19-T COSM4552405 c.558G>A p.K186K Substitution - coding silent 11:65965345-65965345 + pfg181T COSM4756647 c.89C>T p.P30L Substitution - Missense 11:65961869-65961869 + TCGA-E2-A1IH-01 COSM1475770 c.2223G>T p.M741I Substitution - Missense 11:65978650-65978650 + T3021 COSM4723672 c.2305G>A p.V769M Substitution - Missense 11:65978835-65978835 + TCGA-GM-A2DO-01 COSM3810106 c.1806G>A p.E602E Substitution - coding silent 11:65976715-65976715 + 43 COSM3723476 c.1454G>C p.G485A Substitution - Missense 11:65967703-65967703 + TCGA-AP-A0LM-01 COSM930592 c.990T>C p.P330P Substitution - coding silent 11:65966358-65966358 + TCGA-A3-3365-01 COSM1492644 c.2285G>A p.S762N Substitution - Missense 11:65978815-65978815 + T3203 COSM4723670 c.1324C>T p.R442W Substitution - Missense 11:65967481-65967481 + YUOTHO COSM2166937 c.2352C>T p.I784I Substitution - coding silent 11:65978882-65978882 + NCHP_DIPG102 COSM4746275 c.1255C>T p.R419W Substitution - Missense 11:65967325-65967325 + TCGA-D3-A2JL-06 COSM3451934 c.1261G>A p.D421N Substitution - Missense 11:65967331-65967331 + CAL27 COSM2166931 c.2026G>A p.E676K Substitution - Missense 11:65977643-65977643 + T613 COSM4463951 c.1311C>T p.S437S Substitution - coding silent 11:65967381-65967381 + T3094 COSM4723671 c.1723C>T p.R575C Substitution - Missense 11:65976545-65976545 + CSCC-11-T COSM4457433 c.1044C>T p.S348S Substitution - coding silent 11:65966412-65966412 + CSCC-6-T COSM4501274 c.584C>T p.P195L Substitution - Missense 11:65965371-65965371 + RK035_C01 COSM1628171 c.841G>T p.V281L Substitution - Missense 11:65966078-65966078 + TCGA-B7-5816-01 COSM4035602 c.2364C>A p.G788G Substitution - coding silent 11:65978894-65978894 + TCGA-AA-3864-01 COSM5114293 c.2173-10G>A p.? Unknown 11:65978590-65978590 + TCGA-A5-A0GP-01 COSM930595 c.1896G>A p.P632P Substitution - coding silent 11:65977052-65977052 + LUAD-S01315 COSM344050 c.2400G>C p.K800N Substitution - Missense 11:65979027-65979027 + TCGA-14-1823-01 COSM3398053 c.1604G>A p.R535H Substitution - Missense 11:65976426-65976426 + LUAD-NYU1051S COSM368523 c.546A>G p.Q182Q Substitution - coding silent 11:65965210-65965210 + LC_S14 COSM1188307 c.952G>A p.E318K Substitution - Missense 11:65966189-65966189 + TCGA-EE-A2GE-06 COSM3451933 c.1024G>A p.E342K Substitution - Missense 11:65966392-65966392 + T3174 COSM4723669 c.1247T>C p.V416A Substitution - Missense 11:65967317-65967317 + CRC-08T COSM4941443 c.1636G>A p.E546K Substitution - Missense 11:65976458-65976458 + 1N50-VS-1T50 COSM4976523 c.1640G>A p.R547Q Substitution - Missense 11:65976462-65976462 + Pat_06_A COSM5839288 c.697G>T p.V233F Substitution - Missense 11:65965738-65965738 + LOVO COSM2166925 c.1758G>A p.R586R Substitution - coding silent 11:65976667-65976667 + CHC2211T COSM4801122 c.618G>T p.R206S Substitution - Missense 11:65965405-65965405 + TCGA-AC-A23H-01 COSM3810108 c.2170G>T p.E724* Substitution - Nonsense 11:65977897-65977897 + HN_62426 COSM126014 c.1818G>C p.W606C Substitution - Missense 11:65976727-65976727 + T3080 COSM4723665 c.504G>A p.R168R Substitution - coding silent 11:65965168-65965168 + TCGA-BR-7851-01 COSM4035596 c.432G>T p.A144A Substitution - coding silent 11:65965096-65965096 + TCGA-BL-A13I-01 COSM415442 c.22C>G p.R8G Substitution - Missense 11:65961802-65961802 + TCGA-39-5027-01 COSM689946 c.1117C>G p.R373G Substitution - Missense 11:65966485-65966485 + TCGA-BH-A0HX-01 COSM5831829 c.2262+2delT p.? Unknown 11:65978691-65978691 + BD236T COSM5519060 c.2130C>T p.I710I Substitution - coding silent 11:65977857-65977857 + TCGA-JW-A5VL-01 COSM4847415 c.802G>A p.E268K Substitution - Missense 11:65965950-65965950 + Pat_76_A COSM5839287 c.496G>A p.E166K Substitution - Missense 11:65965160-65965160 + Case3c COSM1717504 c.1792T>A p.S598T Substitution - Missense 11:65976701-65976701 + 587376 COSM1224684 c.817A>C p.I273L Substitution - Missense 11:65965965-65965965 + HT115 COSM4638126 c.37G>A p.A13T Substitution - Missense 11:65961817-65961817 + TCGA-09-1669-01 COSM78451 c.2041A>G p.I681V Substitution - Missense 11:65977768-65977768 + SNUH_G16_S1 COSM3676273 c.2238G>T p.R746R Substitution - coding silent 11:65978665-65978665 + ME011T COSM224399 c.805G>A p.G269R Substitution - Missense 11:65965953-65965953 + TCGA-EE-A2MS-06 COSM3451935 c.1336C>T p.R446* Substitution - Nonsense 11:65967493-65967493 + T3058 COSM4723668 c.1049G>A p.R350H Substitution - Missense 11:65966417-65966417 + PTC-7C COSM4146145 c.1853A>G p.Q618R Substitution - Missense 11:65976762-65976762 + 468 COSM4437402 c.2187G>C p.L729L Substitution - coding silent 11:65978614-65978614 + PT30 COSM5906595 c.484C>T p.R162* Substitution - Nonsense 11:65965148-65965148 + TCGA-D1-A169-01 COSM930589 c.661-1G>A p.? Unknown 11:65965701-65965701 + LS411 COSM2166914 c.1211G>T p.R404L Substitution - Missense 11:65967281-65967281 + TCGA-EE-A181-06 COSM3451930 c.48G>A p.T16T Substitution - coding silent 11:65961828-65961828 + CSCC-56-T COSM4463951 c.1311C>T p.S437S Substitution - coding silent 11:65967381-65967381 + TCGA-AM-5821-01 COSM3752649 c.516G>A p.A172A Substitution - coding silent 11:65965180-65965180 + CCK81 COSM4620643 c.1479C>T p.D493D Substitution - coding silent 11:65967728-65967728 + TCGA-JW-A5VL-01 COSM4847370 c.1426G>C p.E476Q Substitution - Missense 11:65967583-65967583 + TCGA-OL-A5S0-01 COSM3810107 c.2072A>G p.Y691C Substitution - Missense 11:65977799-65977799 + TCGA-A2-A1FW-01 COSM1475769 c.1719C>T p.G573G Substitution - coding silent 11:65976541-65976541 + PT42 COSM5925635 c.1043C>T p.S348F Substitution - Missense 11:65966411-65966411 + 12-P412 COSM4574680 c.1322G>T p.G441V Substitution - Missense 11:65967479-65967479 + T3225 COSM4723666 c.533G>A p.R178H Substitution - Missense 11:65965197-65965197 + HCC41 COSM1605049 c.428-4C>G p.? Unknown 11:65965088-65965088 + HRA19 COSM4637640 c.2153G>A p.R718Q Substitution - Missense 11:65977880-65977880 + LUAD-S01404 COSM398680 c.1334G>T p.R445L Substitution - Missense 11:65967491-65967491 + TCGA-AZ-4615-01 COSM3752649 c.516G>A p.A172A Substitution - coding silent 11:65965180-65965180 + TCGA-CG-4442-01 COSM4035603 c.2377A>G p.M793V Substitution - Missense 11:65978907-65978907 + BD72T COSM5512812 c.1639C>T p.R547W Substitution - Missense 11:65976461-65976461 + TCGA-66-2763-01 COSM689945 c.1661A>T p.N554I Substitution - Missense 11:65976483-65976483 + YUOTHO COSM5373296 c.795C>T p.S265S Substitution - coding silent 11:65965943-65965943 + OSCC-GB_01210111 COSM5955027 c.1457_1458CC>TA p.S486L Substitution - Missense 11:65967706-65967707 + TCGA-AD-5900-01 COSM5128422 c.1430-7C>T p.? Unknown 11:65967672-65967672 + TCGA-CG-4476-01 COSM4035599 c.1683C>T p.R561R Substitution - coding silent 11:65976505-65976505 + PCSI_0090_Pa_P COSM3375909 c.1746+4C>T p.? Unknown 11:65976572-65976572 + S02360 COSM5695963 c.2074C>T p.R692* Substitution - Nonsense 11:65977801-65977801 + AOCS-108-1-7 COSM3980577 c.2346C>G p.P782P Substitution - coding silent 11:65978876-65978876 + TCGA-AA-A00J-01 COSM298383 c.1984_1985delAA p.K662fs*16 Deletion - Frameshift 11:65977601-65977602 + 8015299 COSM3769411 c.1484C>T p.A495V Substitution - Missense 11:65967733-65967733 + LUAD-RT-S01702 COSM378972 c.964G>A p.V322M Substitution - Missense 11:65966201-65966201 + HCC074T COSM5810028 c.980A>T p.Q327L Substitution - Missense 11:65966217-65966217 + SC_9028 COSM5554212 c.1304T>C p.F435S Substitution - Missense 11:65967374-65967374 + CSCC-10-T COSM4477064 c.2118C>T p.P706P Substitution - coding silent 11:65977845-65977845 + T3724 COSM4723667 c.621C>T p.S207S Substitution - coding silent 11:65965408-65965408 + TCGA-BR-4184-01 COSM4035598 c.1667C>T p.T556M Substitution - Missense 11:65976489-65976489 + DN11190 COSM5789073 c.1772C>T p.S591L Substitution - Missense 11:65976681-65976681 + C10 COSM4616428 c.1087C>T p.R363W Substitution - Missense 11:65966455-65966455 + PCSI_0090_Pa_X COSM3375909 c.1746+4C>T p.? Unknown 11:65976572-65976572 + TCGA-QL-A97D-01 COSM5188125 c.1164C>T p.S388S Substitution - coding silent 11:65966532-65966532 + PD9467a COSM5789426 c.1250T>C p.V417A Substitution - Missense 11:65967320-65967320 + RKO COSM4647416 c.2174C>T p.A725V Substitution - Missense 11:65978601-65978601 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.502883 11q13.1 605941 2448480|CGAP|BC001058|C/T|coding|Thr258Thr|814|Validated; 862580|dbSNP|BC001058|C/T|coding|Thr258Thr|814|Validated

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G Missense p.I681V c.2041A>G 11 65745239 OV A G Synonymous p.T381T c.1143A>G 11 65733982 LGG A T Missense p.N554I c.1661A>T 11 65743954 LUSC C A Synonymous p.G788G c.2364C>A 11 65746365 STAD CC TT Missense p.S448F c.1343_1344delinsTT 11 65734971 CM C G Missense p.P567A c.1699C>G 11 65743992 LUAD C G Missense p.R373G c.1117C>G 11 65733956 LUSC C G Missense p.R8G c.22C>G 11 65729273 BLCA C T IntronicSNV . c.372-90C>T 11 65731896 CM C T Missense p.A300V c.899C>T 11 65733607 UCEC C T Missense p.P393S c.1177C>T 11 65734016 ESCA C T Nonsense p.R446* c.1336C>T 11 65734964 CM C T Synonymous p.A139A c.417C>T 11 65732031 HNSC C T Synonymous p.D697D c.2091C>T 11 65745289 CM C T Synonymous p.G573G c.1719C>T 11 65744012 BRCA C T Synonymous p.R561R c.1683C>T 11 65743976 STAD G A IntronicSNV . c.2384+43G>A 11 65746428 CM G A Missense p.A300T c.898G>A 11 65733606 BRCA G A Missense p.D421N c.1261G>A 11 65734802 CM G A Missense p.E342K c.1024G>A 11 65733863 CM G A Missense p.G269R c.805G>A 11 65733424 CM G A Missense p.M159I c.477G>A 11 65732612 CM G A Missense p.R467Q c.1400G>A 11 65735028 HNSC G A Missense p.R535H c.1604G>A 11 65743897 GBM G A Missense p.R575H c.1724G>A 11 65744017 HNSC G A Synonymous p.P632P c.1896G>A 11 65744523 UCEC G A Synonymous p.T16T c.48G>A 11 65729299 CM G C Missense p.E284Q c.850G>C 11 65733558 UCEC G C Missense p.K142N c.426G>C 11 65732040 LUAD G C Missense p.W606C c.1818G>C 11 65744198 HNSC G T Missense p.G649V c.1946G>T 11 65745034 CM G T Missense p.M741I c.2223G>T 11 65746121 BRCA G T Missense p.V281L c.841G>T 11 65733549 HC G T Synonymous p.L651L c.1953G>T 11 65745041 LUAD T G Missense p.N138K c.414T>G 11 65732028 MM