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 ACC 11 62561845 62561845 + Missense_Mutation SNP C C T TCGA-OR-A5J5-01A-11D-A29I-10 TCGA-OR-A5J5-10A-01D-A29L-10 g.chr11:62561845C>T c.1645G>A c.(1645-1647)Gct>Act p.A549T BLCA 11 62560121 62560121 + Missense_Mutation SNP G G C TCGA-XF-A9T8-01A-11D-A391-08 TCGA-XF-A9T8-10A-01D-A394-08 g.chr11:62560121G>C c.1813C>G c.(1813-1815)Cat>Gat p.H605D BLCA 11 62560127 62560127 + Missense_Mutation SNP A A C TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr11:62560127A>C c.1807T>G c.(1807-1809)Ttc>Gtc p.F603V BLCA 11 62560155 62560157 + In_Frame_Del DEL GTT GTT - TCGA-DK-A1AD-01A-11D-A13W-08 TCGA-DK-A1AD-10A-01D-A13W-08 g.chr11:62560155_62560157delGTT c.1777_1779delAAC c.(1777-1779)aacdel p.N593del BLCA 11 62561884 62561884 + Missense_Mutation SNP C C G TCGA-G2-A3VY-01A-11D-A22Z-08 TCGA-G2-A3VY-10A-01D-A22Z-08 g.chr11:62561884C>G c.1606G>C c.(1606-1608)Gtg>Ctg p.V536L BLCA 11 62563940 62563940 + Missense_Mutation SNP G G C TCGA-DK-A1AC-01A-11D-A13W-08 TCGA-DK-A1AC-10A-01D-A13W-08 g.chr11:62563940G>C c.1278C>G c.(1276-1278)aaC>aaG p.N426K BLCA 11 62563952 62563952 + Silent SNP G G A TCGA-DK-A3WW-01A-22D-A23M-08 TCGA-DK-A3WW-10A-01D-A23K-08 g.chr11:62563952G>A c.1266C>T c.(1264-1266)ttC>ttT p.F422F BLCA 11 62569095 62569095 + Missense_Mutation SNP C C G TCGA-BT-A20J-01A-11D-A14W-08 TCGA-BT-A20J-11A-11D-A14W-08 g.chr11:62569095C>G c.648G>C c.(646-648)atG>atC p.M216I BLCA 11 62569489 62569489 + Missense_Mutation SNP G G C TCGA-DK-A2I4-01A-11D-A21A-08 TCGA-DK-A2I4-10A-01D-A21A-08 g.chr11:62569489G>C c.483C>G c.(481-483)ttC>ttG p.F161L BLCA 11 62570909 62570909 + Silent SNP C C T TCGA-DK-A2I4-01A-11D-A21A-08 TCGA-DK-A2I4-10A-01D-A21A-08 g.chr11:62570909C>T c.351G>A c.(349-351)aaG>aaA p.K117K BLCA 11 62571417 62571417 + Missense_Mutation SNP C C G TCGA-FD-A6TC-01A-21D-A339-08 TCGA-FD-A6TC-10A-21D-A339-08 g.chr11:62571417C>G c.62G>C c.(61-63)aGa>aCa p.R21T BLCA 11 62571433 62571433 + Missense_Mutation SNP C C T TCGA-4Z-AA7S-01A-11D-A391-08 TCGA-4Z-AA7S-10A-01D-A394-08 g.chr11:62571433C>T c.46G>A c.(46-48)Gtt>Att p.V16I BLCA 11 62572815 62572815 + Missense_Mutation SNP C C G TCGA-FD-A5BR-01A-11D-A26M-08 TCGA-FD-A5BR-10A-01D-A26K-08 g.chr11:62572815C>G c.14G>C c.(13-15)gGg>gCg p.G5A BRCA 11 62561771 62561771 + Silent SNP T T C TCGA-GI-A2C8-01A-11D-A16D-09 TCGA-GI-A2C8-11A-22D-A16D-09 g.chr11:62561771T>C c.1719A>G c.(1717-1719)gcA>gcG p.A573A BRCA 11 62562413 62562413 + Missense_Mutation SNP T T C TCGA-A8-A08P-01A-11W-A019-09 TCGA-A8-A08P-10A-01W-A021-09 g.chr11:62562413T>C c.1571A>G c.(1570-1572)aAt>aGt p.N524S BRCA 11 62564681 62564681 + Missense_Mutation SNP C C G TCGA-A1-A0SI-01A-11D-A142-09 TCGA-A1-A0SI-10B-01D-A142-09 g.chr11:62564681C>G c.1152G>C c.(1150-1152)aaG>aaC p.K384N BRCA 11 62567879 62567879 + Missense_Mutation SNP T T G TCGA-AO-A128-01A-11D-A10M-09 TCGA-AO-A128-10A-01D-A10M-09 g.chr11:62567879T>G c.986A>C c.(985-987)gAc>gCc p.D329A BRCA 11 62567905 62567905 + Silent SNP G G C TCGA-D8-A1JA-01A-11D-A13L-09 TCGA-D8-A1JA-10A-01W-A14R-09 g.chr11:62567905G>C c.960C>G c.(958-960)ctC>ctG p.L320L BRCA 11 62569075 62569075 + Missense_Mutation SNP G G C TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr11:62569075G>C c.668C>G c.(667-669)tCc>tGc p.S223C BRCA 11 62571307 62571307 + Missense_Mutation SNP C C T TCGA-BH-A0HF-01A-11W-A071-09 TCGA-BH-A0HF-10A-01W-A071-09 g.chr11:62571307C>T c.172G>A c.(172-174)Gat>Aat p.D58N BRCA 11 62571388 62571388 + Missense_Mutation SNP A A C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr11:62571388A>C c.91T>G c.(91-93)Tgg>Ggg p.W31G BRCA 11 62572818 62572818 + Missense_Mutation SNP T T C TCGA-A2-A0T5-01A-21D-A099-09 TCGA-A2-A0T5-10A-01D-A099-09 g.chr11:62572818T>C c.11A>G c.(10-12)gAg>gGg p.E4G CESC 11 62567871 62567871 + Silent SNP G G T TCGA-R2-A69V-01A-11D-A32I-09 TCGA-R2-A69V-10A-01D-A32I-09 g.chr11:62567871G>T c.994C>A c.(994-996)Cga>Aga p.R332R CESC 11 62567920 62567920 + Silent SNP C C T TCGA-EA-A3QD-01A-32D-A22X-09 TCGA-EA-A3QD-10A-01D-A22X-09 g.chr11:62567920C>T c.945G>A c.(943-945)ctG>ctA p.L315L CESC 11 62571010 62571010 + Missense_Mutation SNP C C T TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chr11:62571010C>T c.250G>A c.(250-252)Gat>Aat p.D84N CESC 11 62571336 62571336 + Missense_Mutation SNP C C T TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chr11:62571336C>T c.143G>A c.(142-144)cGg>cAg p.R48Q CESC 11 62571352 62571352 + Missense_Mutation SNP C C T TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chr11:62571352C>T c.127G>A c.(127-129)Ggc>Agc p.G43S CESC 11 62571442 62571442 + Missense_Mutation SNP C C G TCGA-FU-A3HY-01A-11D-A21Q-09 TCGA-FU-A3HY-10A-01D-A21Q-09 g.chr11:62571442C>G c.37G>C c.(37-39)Gat>Cat p.D13H CESC 11 62571445 62571445 + Missense_Mutation SNP C C G TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chr11:62571445C>G c.34G>C c.(34-36)Gat>Cat p.D12H COAD 11 62561813 62561813 + Silent SNP C C T TCGA-AA-3956-01A-02W-0995-10 TCGA-AA-3956-10A-01W-0995-10 g.chr11:62561813C>T c.1677G>A c.(1675-1677)ccG>ccA p.P559P COAD 11 62561829 62561829 + Missense_Mutation SNP G G A TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chr11:62561829G>A c.1661C>T c.(1660-1662)aCg>aTg p.T554M COAD 11 62561846 62561846 + Silent SNP G G A TCGA-AA-A02J-01A-01W-A00E-09 TCGA-AA-A02J-10A-01W-A00E-09 g.chr11:62561846G>A c.1644C>T c.(1642-1644)ttC>ttT p.F548F COAD 11 62563395 62563396 + Frame_Shift_Del DEL AG AG - TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr11:62563395_62563396delAG c.1481_1482delCT c.(1480-1482)tctfs p.S494fs COAD 11 62563805 62563805 + Silent SNP G G T TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr11:62563805G>T c.1299C>A c.(1297-1299)gcC>gcA p.A433A COAD 11 62564038 62564038 + Splice_Site SNP A A G TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr11:62564038A>G c.1180T>C c.(1180-1182)Tac>Cac p.Y394H COAD 11 62564673 62564673 + Missense_Mutation SNP A A G TCGA-CM-5344-01A-21D-1719-10 TCGA-CM-5344-10A-01D-1719-10 g.chr11:62564673A>G c.1160T>C c.(1159-1161)gTc>gCc p.V387A COAD 11 62564674 62564674 + Missense_Mutation SNP C C T TCGA-D5-6532-01A-11D-1719-10 TCGA-D5-6532-10A-01D-1719-10 g.chr11:62564674C>T c.1159G>A c.(1159-1161)Gtc>Atc p.V387I COAD 11 62567946 62567946 + Missense_Mutation SNP G G A TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr11:62567946G>A c.919C>T c.(919-921)Cgg>Tgg p.R307W COAD 11 62568633 62568633 + Missense_Mutation SNP A A C TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr11:62568633A>C c.839T>G c.(838-840)cTg>cGg p.L280R COAD 11 62568866 62568866 + Missense_Mutation SNP C C T TCGA-AA-3877-01A-01W-0995-10 TCGA-AA-3877-10A-01W-0995-10 g.chr11:62568866C>T c.733G>A c.(733-735)Gtt>Att p.V245I COAD 11 62570961 62570961 + Missense_Mutation SNP C C A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr11:62570961C>A c.299G>T c.(298-300)aGa>aTa p.R100I COADREAD 11 62561813 62561813 + Silent SNP C C T TCGA-AA-3956-01A-02W-0995-10 TCGA-AA-3956-10A-01W-0995-10 g.chr11:62561813C>T c.1677G>A c.(1675-1677)ccG>ccA p.P559P COADREAD 11 62561829 62561829 + Missense_Mutation SNP G G A TCGA-A6-2676-01A-01W-0833-10 TCGA-A6-2676-10A-01W-0833-10 g.chr11:62561829G>A c.1661C>T c.(1660-1662)aCg>aTg p.T554M COADREAD 11 62561846 62561846 + Silent SNP G G A TCGA-AA-A02J-01A-01W-A00E-09 TCGA-AA-A02J-10A-01W-A00E-09 g.chr11:62561846G>A c.1644C>T c.(1642-1644)ttC>ttT p.F548F COADREAD 11 62563395 62563396 + Frame_Shift_Del DEL AG AG - TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr11:62563395_62563396delAG c.1481_1482delCT c.(1480-1482)tctfs p.S494fs COADREAD 11 62563805 62563805 + Silent SNP G G T TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr11:62563805G>T c.1299C>A c.(1297-1299)gcC>gcA p.A433A COADREAD 11 62564038 62564038 + Splice_Site SNP A A G TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr11:62564038A>G c.1180T>C c.(1180-1182)Tac>Cac p.Y394H COADREAD 11 62564673 62564673 + Missense_Mutation SNP A A G TCGA-CM-5344-01A-21D-1719-10 TCGA-CM-5344-10A-01D-1719-10 g.chr11:62564673A>G c.1160T>C c.(1159-1161)gTc>gCc p.V387A COADREAD 11 62564674 62564674 + Missense_Mutation SNP C C T TCGA-D5-6532-01A-11D-1719-10 TCGA-D5-6532-10A-01D-1719-10 g.chr11:62564674C>T c.1159G>A c.(1159-1161)Gtc>Atc p.V387I COADREAD 11 62566033 62566033 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:62566033C>T c.1031G>A c.(1030-1032)cGa>cAa p.R344Q COADREAD 11 62567946 62567946 + Missense_Mutation SNP G G A TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr11:62567946G>A c.919C>T c.(919-921)Cgg>Tgg p.R307W COADREAD 11 62568633 62568633 + Missense_Mutation SNP A A C TCGA-CA-6718-01A-11D-1835-10 TCGA-CA-6718-10A-01D-1835-10 g.chr11:62568633A>C c.839T>G c.(838-840)cTg>cGg p.L280R COADREAD 11 62568866 62568866 + Missense_Mutation SNP C C T TCGA-AA-3877-01A-01W-0995-10 TCGA-AA-3877-10A-01W-0995-10 g.chr11:62568866C>T c.733G>A c.(733-735)Gtt>Att p.V245I COADREAD 11 62570961 62570961 + Missense_Mutation SNP C C A TCGA-CA-6717-01A-11D-1835-10 TCGA-CA-6717-10A-01D-1835-10 g.chr11:62570961C>A c.299G>T c.(298-300)aGa>aTa p.R100I DLBC 11 62564687 62564687 + Missense_Mutation SNP G G C TCGA-FF-8042-01A-11D-2210-10 TCGA-FF-8042-10A-01D-2210-10 g.chr11:62564687G>C c.1146C>G c.(1144-1146)aaC>aaG p.N382K DLBC 11 62564806 62564806 + Missense_Mutation SNP G G A TCGA-FA-A7Q1-01A-11D-A382-10 TCGA-FA-A7Q1-10A-01D-A385-10 g.chr11:62564806G>A c.1106C>T c.(1105-1107)aCg>aTg p.T369M GBM 11 62561731 62561731 + Splice_Site SNP T T C TCGA-27-1833-01A-01W-0643-08 TCGA-27-1833-10A-01W-0644-08 g.chr11:62561731T>C c.1759A>G c.(1759-1761)Aag>Gag p.K587E GBMLGG 11 62561731 62561731 + Splice_Site SNP T T C TCGA-27-1833-01A-01W-0643-08 TCGA-27-1833-10A-01W-0644-08 g.chr11:62561731T>C c.1759A>G c.(1759-1761)Aag>Gag p.K587E HNSC 11 62561766 62561766 + Missense_Mutation SNP G G A TCGA-T2-A6X2-01A-12D-A34J-08 TCGA-T2-A6X2-10B-01D-A34M-08 g.chr11:62561766G>A c.1724C>T c.(1723-1725)tCt>tTt p.S575F HNSC 11 62561861 62561861 + Silent SNP C C T TCGA-D6-A6EM-01A-21D-A31L-08 TCGA-D6-A6EM-10A-01D-A31J-08 g.chr11:62561861C>T c.1629G>A c.(1627-1629)gaG>gaA p.E543E HNSC 11 62564003 62564003 + Silent SNP C C A TCGA-QK-AA3K-01A-11D-A391-08 TCGA-QK-AA3K-10A-01D-A394-08 g.chr11:62564003C>A c.1215G>T c.(1213-1215)ggG>ggT p.G405G HNSC 11 62564806 62564806 + Missense_Mutation SNP G G A TCGA-CV-7235-01A-11D-2012-08 TCGA-CV-7235-10A-01D-2013-08 g.chr11:62564806G>A c.1106C>T c.(1105-1107)aCg>aTg p.T369M HNSC 11 62567851 62567851 + Silent SNP G G A TCGA-CV-A45P-01A-11D-A24D-08 TCGA-CV-A45P-10A-01D-A24F-08 g.chr11:62567851G>A c.1014C>T c.(1012-1014)atC>atT p.I338I HNSC 11 62569082 62569082 + Missense_Mutation SNP C C T TCGA-CV-6933-01A-11D-1912-08 TCGA-CV-6933-10A-01D-1912-08 g.chr11:62569082C>T c.661G>A c.(661-663)Gat>Aat p.D221N HNSC 11 62571396 62571396 + Missense_Mutation SNP G G A TCGA-CV-7437-01A-21D-2129-08 TCGA-CV-7437-10A-01D-2129-08 g.chr11:62571396G>A c.83C>T c.(82-84)cCc>cTc p.P28L KIPAN 11 62561809 62561809 + Missense_Mutation SNP G G A TCGA-PJ-A8JU-01A-11D-A35Z-10 TCGA-PJ-A8JU-10A-01D-A35Z-10 g.chr11:62561809G>A c.1681C>T c.(1681-1683)Ccc>Tcc p.P561S KIPAN 11 62563986 62563986 + Missense_Mutation SNP T T C TCGA-A4-A772-01A-11D-A33Q-10 TCGA-A4-A772-10A-01D-A33Q-10 g.chr11:62563986T>C c.1232A>G c.(1231-1233)cAt>cGt p.H411R KIPAN 11 62567920 62567921 + Frame_Shift_Ins INS - - G TCGA-AL-3468-01A-01D-1252-08 TCGA-AL-3468-10A-01D-1252-08 g.chr11:62567920_62567921insG c.944_945insC c.(943-945)ctgfs p.L315fs KIPAN 11 62567921 62567921 + Missense_Mutation SNP A A G TCGA-AL-3468-01A-01D-1252-08 TCGA-AL-3468-10A-01D-1252-08 g.chr11:62567921A>G c.944T>C c.(943-945)cTg>cCg p.L315P KIPAN 11 62569079 62569079 + Missense_Mutation SNP C C G TCGA-B0-4816-01A-01D-1501-10 TCGA-B0-4816-11A-02D-1501-10 g.chr11:62569079C>G c.664G>C c.(664-666)Ggc>Cgc p.G222R KIRC 11 62569079 62569079 + Missense_Mutation SNP C C G TCGA-B0-4816-01A-01D-1501-10 TCGA-B0-4816-11A-02D-1501-10 g.chr11:62569079C>G c.664G>C c.(664-666)Ggc>Cgc p.G222R KIRP 11 62561809 62561809 + Missense_Mutation SNP G G A TCGA-PJ-A8JU-01A-11D-A35Z-10 TCGA-PJ-A8JU-10A-01D-A35Z-10 g.chr11:62561809G>A c.1681C>T c.(1681-1683)Ccc>Tcc p.P561S KIRP 11 62563986 62563986 + Missense_Mutation SNP T T C TCGA-A4-A772-01A-11D-A33Q-10 TCGA-A4-A772-10A-01D-A33Q-10 g.chr11:62563986T>C c.1232A>G c.(1231-1233)cAt>cGt p.H411R KIRP 11 62567920 62567921 + Frame_Shift_Ins INS - - G TCGA-AL-3468-01A-01D-1252-08 TCGA-AL-3468-10A-01D-1252-08 g.chr11:62567920_62567921insG c.944_945insC c.(943-945)ctgfs p.L315fs KIRP 11 62567921 62567921 + Missense_Mutation SNP A A G TCGA-AL-3468-01A-01D-1252-08 TCGA-AL-3468-10A-01D-1252-08 g.chr11:62567921A>G c.944T>C c.(943-945)cTg>cCg p.L315P LIHC 11 62560160 62560160 + Missense_Mutation SNP T T A TCGA-EP-A2KC-01A-11D-A20W-10 TCGA-EP-A2KC-10A-01D-A20W-10 g.chr11:62560160T>A c.1774A>T c.(1774-1776)Aac>Tac p.N592Y LIHC 11 62563804 62563804 + Nonsense_Mutation SNP C C A TCGA-DD-AAE6-01A-11D-A40R-10 TCGA-DD-AAE6-10A-01D-A40U-10 g.chr11:62563804C>A c.1300G>T c.(1300-1302)Gag>Tag p.E434* LIHC 11 62566040 62566040 + Missense_Mutation SNP G G C TCGA-DD-A1EH-01A-11D-A12Z-10 TCGA-DD-A1EH-10A-01D-A12Z-10 g.chr11:62566040G>C c.1024C>G c.(1024-1026)Cgc>Ggc p.R342G LUAD 11 62561739 62561739 + Missense_Mutation SNP C C A TCGA-62-8398-01A-11D-2323-08 TCGA-62-8398-10A-01D-2323-08 g.chr11:62561739C>A c.1751G>T c.(1750-1752)tGg>tTg p.W584L LUAD 11 62562464 62562464 + Missense_Mutation SNP C C A TCGA-86-8669-01A-11D-2393-08 TCGA-86-8669-10A-01D-2393-08 g.chr11:62562464C>A c.1520G>T c.(1519-1521)cGg>cTg p.R507L LUAD 11 62563573 62563573 + Missense_Mutation SNP C C G TCGA-69-7974-01A-11D-2184-08 TCGA-69-7974-10A-01D-2184-08 g.chr11:62563573C>G c.1426G>C c.(1426-1428)Gtc>Ctc p.V476L LUAD 11 62566046 62566046 + Splice_Site SNP C C T TCGA-91-6840-01A-11D-1945-08 TCGA-91-6840-10A-01D-1946-08 g.chr11:62566046C>T c.1018G>A c.(1018-1020)Gcc>Acc p.A340T LUAD 11 62568674 62568674 + Splice_Site SNP C C A TCGA-91-6828-01A-11D-1855-08 TCGA-91-6828-10A-01D-1855-08 g.chr11:62568674C>A c.e10-1 LUAD 11 62568824 62568824 + Missense_Mutation SNP T T A TCGA-MP-A4TA-01A-21D-A24P-08 TCGA-MP-A4TA-10A-01D-A24P-08 g.chr11:62568824T>A c.775A>T c.(775-777)Atc>Ttc p.I259F LUAD 11 62569274 62569274 + Silent SNP G G A TCGA-44-2656-01A-02D-0969-08 TCGA-44-2656-10A-01D-0969-08 g.chr11:62569274G>A c.576C>T c.(574-576)aaC>aaT p.N192N LUAD 11 62569425 62569425 + Nonsense_Mutation SNP C C A TCGA-05-4427-01A-21D-1855-08 TCGA-05-4427-10A-01D-1855-08 g.chr11:62569425C>A c.547G>T c.(547-549)Gag>Tag p.E183* LUAD 11 62571028 62571028 + Frame_Shift_Del DEL G G - TCGA-17-Z031-01A-01W-0746-08 TCGA-17-Z031-11A-01W-0746-08 g.chr11:62571028delG c.232delC c.(232-234)cgafs p.R78fs LUAD 11 62571288 62571288 + Missense_Mutation SNP G G A TCGA-91-6828-01A-11D-1855-08 TCGA-91-6828-10A-01D-1855-08 g.chr11:62571288G>A c.191C>T c.(190-192)gCc>gTc p.A64V LUAD 11 62571367 62571367 + Missense_Mutation SNP G G T TCGA-44-8120-01A-11D-2238-08 TCGA-44-8120-10A-01D-2238-08 g.chr11:62571367G>T c.112C>A c.(112-114)Cgt>Agt p.R38S LUAD 11 62571439 62571439 + Missense_Mutation SNP C C G TCGA-55-7903-01A-11D-2167-08 TCGA-55-7903-10A-01D-2167-08 g.chr11:62571439C>G c.40G>C c.(40-42)Gaa>Caa p.E14Q LUSC 11 62568576 62568576 + Missense_Mutation SNP G G C TCGA-66-2754-01A-01D-0983-08 TCGA-66-2754-11A-01D-0983-08 g.chr11:62568576G>C c.896C>G c.(895-897)tCt>tGt p.S299C LUSC 11 62568599 62568599 + Silent SNP G G T TCGA-66-2787-01A-01D-0983-08 TCGA-66-2787-11A-01D-0983-08 g.chr11:62568599G>T c.873C>A c.(871-873)ccC>ccA p.P291P LUSC 11 62569222 62569222 + Missense_Mutation SNP C C T TCGA-66-2742-01A-01D-0983-08 TCGA-66-2742-11A-01D-0983-08 g.chr11:62569222C>T c.628G>A c.(628-630)Gaa>Aaa p.E210K PRAD 11 62569242 62569242 + Missense_Mutation SNP T T A TCGA-KK-A8ID-01A-11D-A364-08 TCGA-KK-A8ID-11A-12D-A362-08 g.chr11:62569242T>A c.608A>T c.(607-609)gAa>gTa p.E203V READ 11 62566033 62566033 + Missense_Mutation SNP C C T TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr11:62566033C>T c.1031G>A c.(1030-1032)cGa>cAa p.R344Q SARC 11 62568587 62568587 + Silent SNP G G A TCGA-QQ-A8VG-01A-11D-A37C-09 TCGA-QQ-A8VG-10A-01D-A37F-09 g.chr11:62568587G>A c.885C>T c.(883-885)atC>atT p.I295I SARC 11 62568890 62568890 + Splice_Site SNP C C T TCGA-QC-A7B5-01A-11D-A33E-09 TCGA-QC-A7B5-11A-11D-A33H-09 g.chr11:62568890C>T c.e9-1 SKCM 11 62562413 62562413 + Missense_Mutation SNP T T A TCGA-D3-A5GS-06A-11D-A27K-08 TCGA-D3-A5GS-10A-01D-A27N-08 g.chr11:62562413T>A c.1571A>T c.(1570-1572)aAt>aTt p.N524I SKCM 11 62562463 62562463 + Silent SNP C C T TCGA-D3-A2JA-06A-11D-A196-08 TCGA-D3-A2JA-10A-01D-A198-08 g.chr11:62562463C>T c.1521G>A c.(1519-1521)cgG>cgA p.R507R SKCM 11 62562464 62562464 + Missense_Mutation SNP C C T TCGA-D3-A2JA-06A-11D-A196-08 TCGA-D3-A2JA-10A-01D-A198-08 g.chr11:62562464C>T c.1520G>A c.(1519-1521)cGg>cAg p.R507Q SKCM 11 62564692 62564692 + Missense_Mutation SNP C C T TCGA-ER-A19M-06A-61D-A23B-08 TCGA-ER-A19M-10A-01D-A23B-08 g.chr11:62564692C>T c.1141G>A c.(1141-1143)Gaa>Aaa p.E381K SKCM 11 62566040 62566040 + Missense_Mutation SNP G G A TCGA-ER-A19Q-06A-11D-A197-08 TCGA-ER-A19Q-10A-01D-A199-08 g.chr11:62566040G>A c.1024C>T c.(1024-1026)Cgc>Tgc p.R342C SKCM 11 62569260 62569260 + Missense_Mutation SNP G G A TCGA-FS-A4F5-06A-11D-A25O-08 TCGA-FS-A4F5-10B-01D-A25O-08 g.chr11:62569260G>A c.590C>T c.(589-591)cCc>cTc p.P197L SKCM 11 62569486 62569486 + Silent SNP G G A TCGA-DA-A1I4-06A-11D-A196-08 TCGA-DA-A1I4-10A-01D-A198-08 g.chr11:62569486G>A c.486C>T c.(484-486)ttC>ttT p.F162F

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-CN 11 62554974 62554974 single base substitution C T downstream_gene_variant BLCA-US 11 62557492 62557492 single base substitution C T downstream_gene_variant BLCA-US 11 62560155 62560157 deletion of <=200bp GTT - 3_prime_UTR_variant BLCA-US 11 62560155 62560157 deletion of <=200bp GTT - downstream_gene_variant BLCA-US 11 62560155 62560157 deletion of <=200bp GTT - exon_variant BLCA-US 11 62560155 62560157 deletion of <=200bp GTT - inframe_deletion N593 BLCA-US 11 62560155 62560157 deletion of <=200bp GTT - inframe_deletion N97 BLCA-US 11 62561884 62561884 single base substitution C G 3_prime_UTR_variant BLCA-US 11 62561884 62561884 single base substitution C G downstream_gene_variant BLCA-US 11 62561884 62561884 single base substitution C G exon_variant BLCA-US 11 62561884 62561884 single base substitution C G intron_variant BLCA-US 11 62561884 62561884 single base substitution C G missense_variant V536L 1606G>C BLCA-US 11 62561884 62561884 single base substitution C G missense_variant V579L 1735G>C BLCA-US 11 62563940 62563940 single base substitution G C 3_prime_UTR_variant BLCA-US 11 62563940 62563940 single base substitution G C downstream_gene_variant BLCA-US 11 62563940 62563940 single base substitution G C exon_variant BLCA-US 11 62563940 62563940 single base substitution G C intron_variant BLCA-US 11 62563940 62563940 single base substitution G C missense_variant N426K 1278C>G BLCA-US 11 62563940 62563940 single base substitution G C missense_variant N469K 1407C>G BLCA-US 11 62563940 62563940 single base substitution G C upstream_gene_variant BLCA-US 11 62563952 62563952 single base substitution G A 3_prime_UTR_variant BLCA-US 11 62563952 62563952 single base substitution G A downstream_gene_variant BLCA-US 11 62563952 62563952 single base substitution G A exon_variant BLCA-US 11 62563952 62563952 single base substitution G A intron_variant BLCA-US 11 62563952 62563952 single base substitution G A synonymous_variant F422F 1266C>T BLCA-US 11 62563952 62563952 single base substitution G A synonymous_variant F465F 1395C>T BLCA-US 11 62563952 62563952 single base substitution G A upstream_gene_variant BLCA-US 11 62569095 62569095 single base substitution C G downstream_gene_variant BLCA-US 11 62569095 62569095 single base substitution C G intron_variant BLCA-US 11 62569095 62569095 single base substitution C G missense_variant M216I 648G>C BLCA-US 11 62569095 62569095 single base substitution C G missense_variant M259I 777G>C BLCA-US 11 62569095 62569095 single base substitution C G missense_variant M79I 237G>C BLCA-US 11 62569095 62569095 single base substitution C G upstream_gene_variant BLCA-US 11 62569489 62569489 single base substitution G C 3_prime_UTR_variant BLCA-US 11 62569489 62569489 single base substitution G C downstream_gene_variant BLCA-US 11 62569489 62569489 single base substitution G C intron_variant BLCA-US 11 62569489 62569489 single base substitution G C missense_variant F101L 303C>G BLCA-US 11 62569489 62569489 single base substitution G C missense_variant F161L 483C>G BLCA-US 11 62569489 62569489 single base substitution G C missense_variant F204L 612C>G BLCA-US 11 62569489 62569489 single base substitution G C missense_variant F24L 72C>G BLCA-US 11 62569489 62569489 single base substitution G C upstream_gene_variant BLCA-US 11 62570909 62570909 single base substitution C T 3_prime_UTR_variant BLCA-US 11 62570909 62570909 single base substitution C T downstream_gene_variant BLCA-US 11 62570909 62570909 single base substitution C T intron_variant BLCA-US 11 62570909 62570909 single base substitution C T synonymous_variant K117K 351G>A BLCA-US 11 62570909 62570909 single base substitution C T synonymous_variant K160K 480G>A BLCA-US 11 62570909 62570909 single base substitution C T synonymous_variant K57K 171G>A BLCA-US 11 62570909 62570909 single base substitution C T upstream_gene_variant BLCA-US 11 62575050 62575050 single base substitution G C upstream_gene_variant BRCA-EU 11 62554777 62554777 single base substitution C T downstream_gene_variant BRCA-EU 11 62554795 62554795 single base substitution A G downstream_gene_variant BRCA-EU 11 62554966 62554966 single base substitution G A downstream_gene_variant BRCA-EU 11 62555613 62555613 single base substitution G A downstream_gene_variant BRCA-EU 11 62560323 62560323 single base substitution G C downstream_gene_variant BRCA-EU 11 62560323 62560323 single base substitution G C intron_variant BRCA-EU 11 62561061 62561061 single base substitution A T downstream_gene_variant BRCA-EU 11 62561061 62561061 single base substitution A T intron_variant BRCA-EU 11 62561190 62561190 single base substitution T C downstream_gene_variant BRCA-EU 11 62561190 62561190 single base substitution T C intron_variant BRCA-EU 11 62561390 62561390 single base substitution T C downstream_gene_variant BRCA-EU 11 62561390 62561390 single base substitution T C intron_variant BRCA-EU 11 62561694 62561694 single base substitution C T downstream_gene_variant BRCA-EU 11 62561694 62561694 single base substitution C T intron_variant BRCA-EU 11 62562293 62562293 single base substitution C T downstream_gene_variant BRCA-EU 11 62562293 62562293 single base substitution C T exon_variant BRCA-EU 11 62562293 62562293 single base substitution C T intron_variant BRCA-EU 11 62562293 62562293 single base substitution C T upstream_gene_variant BRCA-EU 11 62562323 62562323 single base substitution C G downstream_gene_variant BRCA-EU 11 62562323 62562323 single base substitution C G exon_variant BRCA-EU 11 62562323 62562323 single base substitution C G intron_variant BRCA-EU 11 62562323 62562323 single base substitution C G upstream_gene_variant BRCA-EU 11 62565128 62565128 single base substitution C T downstream_gene_variant BRCA-EU 11 62565128 62565128 single base substitution C T intron_variant BRCA-EU 11 62565128 62565128 single base substitution C T upstream_gene_variant BRCA-EU 11 62566202 62566202 single base substitution C A 3_prime_UTR_variant BRCA-EU 11 62566202 62566202 single base substitution C A downstream_gene_variant BRCA-EU 11 62566202 62566202 single base substitution C A intron_variant BRCA-EU 11 62566202 62566202 single base substitution C A upstream_gene_variant BRCA-EU 11 62566276 62566276 single base substitution G C 3_prime_UTR_variant BRCA-EU 11 62566276 62566276 single base substitution G C downstream_gene_variant BRCA-EU 11 62566276 62566276 single base substitution G C intron_variant BRCA-EU 11 62566276 62566276 single base substitution G C upstream_gene_variant BRCA-EU 11 62568257 62568257 insertion of <=200bp - A downstream_gene_variant BRCA-EU 11 62568257 62568257 insertion of <=200bp - A intron_variant BRCA-EU 11 62568257 62568257 insertion of <=200bp - A upstream_gene_variant BRCA-EU 11 62569418 62569418 single base substitution C T downstream_gene_variant BRCA-EU 11 62569418 62569418 single base substitution C T intron_variant BRCA-EU 11 62569418 62569418 single base substitution C T missense_variant R185Q 554G>A BRCA-EU 11 62569418 62569418 single base substitution C T missense_variant R228Q 683G>A BRCA-EU 11 62569418 62569418 single base substitution C T missense_variant R48Q 143G>A BRCA-EU 11 62569418 62569418 single base substitution C T upstream_gene_variant BRCA-EU 11 62569525 62569525 single base substitution G C downstream_gene_variant BRCA-EU 11 62569525 62569525 single base substitution G C intron_variant BRCA-EU 11 62569525 62569525 single base substitution G C splice_region_variant BRCA-EU 11 62569525 62569525 single base substitution G C upstream_gene_variant BRCA-EU 11 62569904 62569904 single base substitution C G downstream_gene_variant BRCA-EU 11 62569904 62569904 single base substitution C G intron_variant BRCA-EU 11 62569904 62569904 single base substitution C G upstream_gene_variant BRCA-EU 11 62570011 62570011 single base substitution C T downstream_gene_variant BRCA-EU 11 62570011 62570011 single base substitution C T intron_variant BRCA-EU 11 62570011 62570011 single base substitution C T upstream_gene_variant BRCA-EU 11 62570230 62570230 deletion of <=200bp A - downstream_gene_variant BRCA-EU 11 62570230 62570230 deletion of <=200bp A - intron_variant BRCA-EU 11 62570230 62570230 deletion of <=200bp A - upstream_gene_variant BRCA-EU 11 62570940 62570940 single base substitution C T 3_prime_UTR_variant BRCA-EU 11 62570940 62570940 single base substitution C T downstream_gene_variant BRCA-EU 11 62570940 62570940 single base substitution C T intron_variant BRCA-EU 11 62570940 62570940 single base substitution C T missense_variant G107E 320G>A BRCA-EU 11 62570940 62570940 single base substitution C T missense_variant G150E 449G>A BRCA-EU 11 62570940 62570940 single base substitution C T missense_variant G47E 140G>A BRCA-EU 11 62570940 62570940 single base substitution C T upstream_gene_variant BRCA-EU 11 62571673 62571673 single base substitution G T intron_variant BRCA-EU 11 62571673 62571673 single base substitution G T stop_gained S13* 38C>A BRCA-EU 11 62571673 62571673 single base substitution G T upstream_gene_variant BRCA-EU 11 62572997 62572997 single base substitution C T 5_prime_UTR_variant BRCA-EU 11 62572997 62572997 single base substitution C T upstream_gene_variant BRCA-EU 11 62573167 62573167 single base substitution G C 5_prime_UTR_premature_start_codon_gain_variant BRCA-EU 11 62573167 62573167 single base substitution G C upstream_gene_variant BRCA-EU 11 62573341 62573341 single base substitution C T 5_prime_UTR_variant BRCA-EU 11 62573341 62573341 single base substitution C T upstream_gene_variant BRCA-EU 11 62573592 62573592 single base substitution C T intron_variant BRCA-EU 11 62573592 62573592 single base substitution C T upstream_gene_variant BRCA-EU 11 62574893 62574893 single base substitution C A upstream_gene_variant BRCA-EU 11 62576061 62576061 single base substitution A C upstream_gene_variant BRCA-EU 11 62576536 62576536 single base substitution C A upstream_gene_variant BRCA-EU 11 62576934 62576934 single base substitution C T upstream_gene_variant BRCA-EU 11 62577325 62577325 single base substitution C T upstream_gene_variant BRCA-FR 11 62554777 62554777 single base substitution C T downstream_gene_variant BRCA-FR 11 62558556 62558556 single base substitution G C downstream_gene_variant BRCA-FR 11 62573592 62573592 single base substitution C T intron_variant BRCA-FR 11 62573592 62573592 single base substitution C T upstream_gene_variant BRCA-FR 11 62576934 62576934 single base substitution C T upstream_gene_variant BRCA-UK 11 62557686 62557686 single base substitution G A downstream_gene_variant BRCA-UK 11 62572819 62572819 single base substitution C T 5_prime_UTR_variant BRCA-UK 11 62572819 62572819 single base substitution C T exon_variant BRCA-UK 11 62572819 62572819 single base substitution C T missense_variant E4K 10G>A BRCA-UK 11 62572819 62572819 single base substitution C T upstream_gene_variant BRCA-US 11 62554930 62554930 single base substitution C T downstream_gene_variant BRCA-US 11 62556503 62556503 single base substitution C G downstream_gene_variant BRCA-US 11 62558104 62558104 single base substitution C G downstream_gene_variant BRCA-US 11 62559273 62559273 insertion of <=200bp - C downstream_gene_variant BRCA-US 11 62559276 62559276 single base substitution A T downstream_gene_variant BRCA-US 11 62559918 62559918 deletion of <=200bp G - 3_prime_UTR_variant BRCA-US 11 62559918 62559918 deletion of <=200bp G - downstream_gene_variant BRCA-US 11 62559918 62559918 deletion of <=200bp G - exon_variant BRCA-US 11 62561771 62561771 single base substitution T C 3_prime_UTR_variant BRCA-US 11 62561771 62561771 single base substitution T C downstream_gene_variant BRCA-US 11 62561771 62561771 single base substitution T C exon_variant BRCA-US 11 62561771 62561771 single base substitution T C synonymous_variant A573A 1719A>G BRCA-US 11 62561771 62561771 single base substitution T C synonymous_variant A77A 231A>G BRCA-US 11 62562413 62562413 single base substitution T C 3_prime_UTR_variant BRCA-US 11 62562413 62562413 single base substitution T C downstream_gene_variant BRCA-US 11 62562413 62562413 single base substitution T C exon_variant BRCA-US 11 62562413 62562413 single base substitution T C missense_variant N42S 125A>G BRCA-US 11 62562413 62562413 single base substitution T C missense_variant N524S 1571A>G BRCA-US 11 62562413 62562413 single base substitution T C missense_variant N567S 1700A>G BRCA-US 11 62562413 62562413 single base substitution T C upstream_gene_variant BRCA-US 11 62564681 62564681 single base substitution C G 3_prime_UTR_variant BRCA-US 11 62564681 62564681 single base substitution C G downstream_gene_variant BRCA-US 11 62564681 62564681 single base substitution C G exon_variant BRCA-US 11 62564681 62564681 single base substitution C G missense_variant K384N 1152G>C BRCA-US 11 62564681 62564681 single base substitution C G missense_variant K427N 1281G>C BRCA-US 11 62564681 62564681 single base substitution C G upstream_gene_variant BRCA-US 11 62567879 62567879 single base substitution T G downstream_gene_variant BRCA-US 11 62567879 62567879 single base substitution T G exon_variant BRCA-US 11 62567879 62567879 single base substitution T G intron_variant BRCA-US 11 62567879 62567879 single base substitution T G missense_variant D192A 575A>C BRCA-US 11 62567879 62567879 single base substitution T G missense_variant D329A 986A>C BRCA-US 11 62567879 62567879 single base substitution T G missense_variant D372A 1115A>C BRCA-US 11 62567879 62567879 single base substitution T G upstream_gene_variant BRCA-US 11 62567905 62567905 single base substitution G C downstream_gene_variant BRCA-US 11 62567905 62567905 single base substitution G C exon_variant BRCA-US 11 62567905 62567905 single base substitution G C intron_variant BRCA-US 11 62567905 62567905 single base substitution G C synonymous_variant L183L 549C>G BRCA-US 11 62567905 62567905 single base substitution G C synonymous_variant L320L 960C>G BRCA-US 11 62567905 62567905 single base substitution G C synonymous_variant L363L 1089C>G BRCA-US 11 62567905 62567905 single base substitution G C upstream_gene_variant BRCA-US 11 62569075 62569075 single base substitution G C downstream_gene_variant BRCA-US 11 62569075 62569075 single base substitution G C intron_variant BRCA-US 11 62569075 62569075 single base substitution G C missense_variant S223C 668C>G BRCA-US 11 62569075 62569075 single base substitution G C missense_variant S266C 797C>G BRCA-US 11 62569075 62569075 single base substitution G C missense_variant S86C 257C>G BRCA-US 11 62569075 62569075 single base substitution G C upstream_gene_variant BRCA-US 11 62571307 62571307 single base substitution C T 5_prime_UTR_variant BRCA-US 11 62571307 62571307 single base substitution C T exon_variant BRCA-US 11 62571307 62571307 single base substitution C T intron_variant BRCA-US 11 62571307 62571307 single base substitution C T missense_variant D101N 301G>A BRCA-US 11 62571307 62571307 single base substitution C T missense_variant D58N 172G>A BRCA-US 11 62571388 62571388 single base substitution A C 5_prime_UTR_variant BRCA-US 11 62571388 62571388 single base substitution A C exon_variant BRCA-US 11 62571388 62571388 single base substitution A C intron_variant BRCA-US 11 62571388 62571388 single base substitution A C missense_variant W31G 91T>G BRCA-US 11 62571388 62571388 single base substitution A C missense_variant W74G 220T>G BRCA-US 11 62572818 62572818 single base substitution T C 5_prime_UTR_variant BRCA-US 11 62572818 62572818 single base substitution T C exon_variant BRCA-US 11 62572818 62572818 single base substitution T C missense_variant E4G 11A>G BRCA-US 11 62572818 62572818 single base substitution T C upstream_gene_variant BRCA-US 11 62572858 62572858 single base substitution G A 5_prime_UTR_variant BRCA-US 11 62572858 62572858 single base substitution G A exon_variant BRCA-US 11 62572858 62572858 single base substitution G A upstream_gene_variant BRCA-US 11 62572890 62572890 single base substitution T C 5_prime_UTR_variant BRCA-US 11 62572890 62572890 single base substitution T C exon_variant BRCA-US 11 62572890 62572890 single base substitution T C upstream_gene_variant BRCA-US 11 62574965 62574965 single base substitution G T upstream_gene_variant BTCA-JP 11 62555494 62555494 single base substitution C G downstream_gene_variant BTCA-JP 11 62562581 62562582 deletion of <=200bp AG - downstream_gene_variant BTCA-JP 11 62562581 62562582 deletion of <=200bp AG - exon_variant BTCA-JP 11 62562581 62562582 deletion of <=200bp AG - intron_variant BTCA-JP 11 62562581 62562582 deletion of <=200bp AG - upstream_gene_variant BTCA-JP 11 62564703 62564703 single base substitution T C 3_prime_UTR_variant BTCA-JP 11 62564703 62564703 single base substitution T C downstream_gene_variant BTCA-JP 11 62564703 62564703 single base substitution T C exon_variant BTCA-JP 11 62564703 62564703 single base substitution T C missense_variant Y377C 1130A>G BTCA-JP 11 62564703 62564703 single base substitution T C missense_variant Y420C 1259A>G BTCA-JP 11 62564703 62564703 single base substitution T C upstream_gene_variant BTCA-JP 11 62567954 62567954 single base substitution T G downstream_gene_variant BTCA-JP 11 62567954 62567954 single base substitution T G exon_variant BTCA-JP 11 62567954 62567954 single base substitution T G intron_variant BTCA-JP 11 62567954 62567954 single base substitution T G missense_variant K167T 500A>C BTCA-JP 11 62567954 62567954 single base substitution T G missense_variant K304T 911A>C BTCA-JP 11 62567954 62567954 single base substitution T G missense_variant K347T 1040A>C BTCA-JP 11 62567954 62567954 single base substitution T G upstream_gene_variant BTCA-JP 11 62568077 62568077 single base substitution C T downstream_gene_variant BTCA-JP 11 62568077 62568077 single base substitution C T intron_variant BTCA-JP 11 62568077 62568077 single base substitution C T upstream_gene_variant BTCA-JP 11 62569765 62569765 single base substitution G A downstream_gene_variant BTCA-JP 11 62569765 62569765 single base substitution G A intron_variant BTCA-JP 11 62569765 62569765 single base substitution G A upstream_gene_variant BTCA-JP 11 62572893 62572893 single base substitution C T 5_prime_UTR_variant BTCA-JP 11 62572893 62572893 single base substitution C T exon_variant BTCA-JP 11 62572893 62572893 single base substitution C T upstream_gene_variant CESC-US 11 62554674 62554674 single base substitution C G downstream_gene_variant CESC-US 11 62558226 62558226 single base substitution G A downstream_gene_variant CESC-US 11 62567871 62567871 single base substitution G T downstream_gene_variant CESC-US 11 62567871 62567871 single base substitution G T exon_variant CESC-US 11 62567871 62567871 single base substitution G T intron_variant CESC-US 11 62567871 62567871 single base substitution G T synonymous_variant R195R 583C>A CESC-US 11 62567871 62567871 single base substitution G T synonymous_variant R332R 994C>A CESC-US 11 62567871 62567871 single base substitution G T synonymous_variant R375R 1123C>A CESC-US 11 62567871 62567871 single base substitution G T upstream_gene_variant CESC-US 11 62567920 62567920 single base substitution C T downstream_gene_variant CESC-US 11 62567920 62567920 single base substitution C T exon_variant CESC-US 11 62567920 62567920 single base substitution C T intron_variant CESC-US 11 62567920 62567920 single base substitution C T synonymous_variant L178L 534G>A CESC-US 11 62567920 62567920 single base substitution C T synonymous_variant L315L 945G>A CESC-US 11 62567920 62567920 single base substitution C T synonymous_variant L358L 1074G>A CESC-US 11 62567920 62567920 single base substitution C T upstream_gene_variant CESC-US 11 62571010 62571010 single base substitution C T 3_prime_UTR_variant CESC-US 11 62571010 62571010 single base substitution C T downstream_gene_variant CESC-US 11 62571010 62571010 single base substitution C T intron_variant CESC-US 11 62571010 62571010 single base substitution C T missense_variant D127N 379G>A CESC-US 11 62571010 62571010 single base substitution C T missense_variant D24N 70G>A CESC-US 11 62571010 62571010 single base substitution C T missense_variant D84N 250G>A CESC-US 11 62571010 62571010 single base substitution C T upstream_gene_variant CESC-US 11 62571336 62571336 single base substitution C T 5_prime_UTR_variant CESC-US 11 62571336 62571336 single base substitution C T exon_variant CESC-US 11 62571336 62571336 single base substitution C T intron_variant CESC-US 11 62571336 62571336 single base substitution C T missense_variant R48Q 143G>A CESC-US 11 62571336 62571336 single base substitution C T missense_variant R91Q 272G>A CESC-US 11 62571352 62571352 single base substitution C T 5_prime_UTR_variant CESC-US 11 62571352 62571352 single base substitution C T exon_variant CESC-US 11 62571352 62571352 single base substitution C T intron_variant CESC-US 11 62571352 62571352 single base substitution C T missense_variant G43S 127G>A CESC-US 11 62571352 62571352 single base substitution C T missense_variant G86S 256G>A CESC-US 11 62571442 62571442 single base substitution C G 5_prime_UTR_variant CESC-US 11 62571442 62571442 single base substitution C G exon_variant CESC-US 11 62571442 62571442 single base substitution C G intron_variant CESC-US 11 62571442 62571442 single base substitution C G missense_variant D13H 37G>C CESC-US 11 62571442 62571442 single base substitution C G missense_variant D56H 166G>C CESC-US 11 62571445 62571445 single base substitution C G 5_prime_UTR_variant CESC-US 11 62571445 62571445 single base substitution C G exon_variant CESC-US 11 62571445 62571445 single base substitution C G intron_variant CESC-US 11 62571445 62571445 single base substitution C G missense_variant D12H 34G>C CESC-US 11 62571445 62571445 single base substitution C G missense_variant D55H 163G>C CESC-US 11 62572855 62572855 single base substitution C T 5_prime_UTR_variant CESC-US 11 62572855 62572855 single base substitution C T exon_variant CESC-US 11 62572855 62572855 single base substitution C T upstream_gene_variant CESC-US 11 62575156 62575156 single base substitution C T upstream_gene_variant CLLE-ES 11 62569215 62569215 single base substitution A C downstream_gene_variant CLLE-ES 11 62569215 62569215 single base substitution A C intron_variant CLLE-ES 11 62569215 62569215 single base substitution A C missense_variant L212R 635T>G CLLE-ES 11 62569215 62569215 single base substitution A C missense_variant L255R 764T>G CLLE-ES 11 62569215 62569215 single base substitution A C missense_variant L75R 224T>G CLLE-ES 11 62569215 62569215 single base substitution A C upstream_gene_variant CLLE-ES 11 62571028 62571028 single base substitution G A exon_variant CLLE-ES 11 62571028 62571028 single base substitution G A intron_variant CLLE-ES 11 62571028 62571028 single base substitution G A stop_gained R121* 361C>T CLLE-ES 11 62571028 62571028 single base substitution G A stop_gained R18* 52C>T CLLE-ES 11 62571028 62571028 single base substitution G A stop_gained R78* 232C>T CLLE-ES 11 62571028 62571028 single base substitution G A upstream_gene_variant CLLE-ES 11 62571415 62571415 single base substitution T A 5_prime_UTR_variant CLLE-ES 11 62571415 62571415 single base substitution T A exon_variant CLLE-ES 11 62571415 62571415 single base substitution T A intron_variant CLLE-ES 11 62571415 62571415 single base substitution T A stop_gained K22* 64A>T CLLE-ES 11 62571415 62571415 single base substitution T A stop_gained K65* 193A>T COAD-US 11 62557412 62557412 single base substitution G A downstream_gene_variant COAD-US 11 62559270 62559270 insertion of <=200bp - C downstream_gene_variant COAD-US 11 62559340 62559340 single base substitution G A downstream_gene_variant COAD-US 11 62563805 62563805 single base substitution G T 3_prime_UTR_variant COAD-US 11 62563805 62563805 single base substitution G T downstream_gene_variant COAD-US 11 62563805 62563805 single base substitution G T exon_variant COAD-US 11 62563805 62563805 single base substitution G T synonymous_variant A433A 1299C>A COAD-US 11 62563805 62563805 single base substitution G T synonymous_variant A476A 1428C>A COAD-US 11 62563805 62563805 single base substitution G T upstream_gene_variant COAD-US 11 62568633 62568633 single base substitution A C downstream_gene_variant COAD-US 11 62568633 62568633 single base substitution A C intron_variant COAD-US 11 62568633 62568633 single base substitution A C missense_variant L143R 428T>G COAD-US 11 62568633 62568633 single base substitution A C missense_variant L280R 839T>G COAD-US 11 62568633 62568633 single base substitution A C missense_variant L323R 968T>G COAD-US 11 62568633 62568633 single base substitution A C upstream_gene_variant COAD-US 11 62575072 62575072 single base substitution G A upstream_gene_variant COCA-CN 11 62557265 62557265 single base substitution C T downstream_gene_variant COCA-CN 11 62558248 62558248 single base substitution C T downstream_gene_variant COCA-CN 11 62558289 62558289 single base substitution C T downstream_gene_variant COCA-CN 11 62563744 62563744 single base substitution G A downstream_gene_variant COCA-CN 11 62563744 62563744 single base substitution G A intron_variant COCA-CN 11 62563744 62563744 single base substitution G A upstream_gene_variant COCA-CN 11 62564413 62564413 single base substitution C T downstream_gene_variant COCA-CN 11 62564413 62564413 single base substitution C T intron_variant COCA-CN 11 62564413 62564413 single base substitution C T splice_donor_variant COCA-CN 11 62564413 62564413 single base substitution C T upstream_gene_variant COCA-CN 11 62564556 62564556 single base substitution C A downstream_gene_variant COCA-CN 11 62564556 62564556 single base substitution C A intron_variant COCA-CN 11 62564556 62564556 single base substitution C A upstream_gene_variant COCA-CN 11 62566030 62566030 single base substitution A G 3_prime_UTR_variant COCA-CN 11 62566030 62566030 single base substitution A G downstream_gene_variant COCA-CN 11 62566030 62566030 single base substitution A G exon_variant COCA-CN 11 62566030 62566030 single base substitution A G intron_variant COCA-CN 11 62566030 62566030 single base substitution A G missense_variant F345S 1034T>C COCA-CN 11 62566030 62566030 single base substitution A G missense_variant F388S 1163T>C COCA-CN 11 62566030 62566030 single base substitution A G upstream_gene_variant COCA-CN 11 62568480 62568480 single base substitution C T downstream_gene_variant COCA-CN 11 62568480 62568480 single base substitution C T intron_variant COCA-CN 11 62568480 62568480 single base substitution C T upstream_gene_variant EOPC-DE 11 62560199 62560199 single base substitution G A downstream_gene_variant EOPC-DE 11 62560199 62560199 single base substitution G A intron_variant EOPC-DE 11 62564638 62564638 single base substitution G C downstream_gene_variant EOPC-DE 11 62564638 62564638 single base substitution G C intron_variant EOPC-DE 11 62564638 62564638 single base substitution G C upstream_gene_variant ESAD-UK 11 62557557 62557557 single base substitution T A downstream_gene_variant ESAD-UK 11 62562373 62562373 single base substitution G A downstream_gene_variant ESAD-UK 11 62562373 62562373 single base substitution G A exon_variant ESAD-UK 11 62562373 62562373 single base substitution G A intron_variant ESAD-UK 11 62562373 62562373 single base substitution G A upstream_gene_variant ESAD-UK 11 62563055 62563055 single base substitution G A downstream_gene_variant ESAD-UK 11 62563055 62563055 single base substitution G A intron_variant ESAD-UK 11 62563055 62563055 single base substitution G A upstream_gene_variant ESAD-UK 11 62563466 62563466 single base substitution G A downstream_gene_variant ESAD-UK 11 62563466 62563466 single base substitution G A intron_variant ESAD-UK 11 62563466 62563466 single base substitution G A upstream_gene_variant ESAD-UK 11 62563467 62563467 single base substitution C A downstream_gene_variant ESAD-UK 11 62563467 62563467 single base substitution C A intron_variant ESAD-UK 11 62563467 62563467 single base substitution C A upstream_gene_variant ESAD-UK 11 62564376 62564376 single base substitution G A downstream_gene_variant ESAD-UK 11 62564376 62564376 single base substitution G A intron_variant ESAD-UK 11 62564376 62564376 single base substitution G A upstream_gene_variant ESAD-UK 11 62565758 62565758 single base substitution G A downstream_gene_variant ESAD-UK 11 62565758 62565758 single base substitution G A intron_variant ESAD-UK 11 62565758 62565758 single base substitution G A upstream_gene_variant ESAD-UK 11 62565929 62565929 single base substitution G T downstream_gene_variant ESAD-UK 11 62565929 62565929 single base substitution G T intron_variant ESAD-UK 11 62565929 62565929 single base substitution G T upstream_gene_variant ESAD-UK 11 62568047 62568047 single base substitution G T downstream_gene_variant ESAD-UK 11 62568047 62568047 single base substitution G T intron_variant ESAD-UK 11 62568047 62568047 single base substitution G T upstream_gene_variant ESAD-UK 11 62573216 62573216 single base substitution G A 5_prime_UTR_variant ESAD-UK 11 62573216 62573216 single base substitution G A upstream_gene_variant ESAD-UK 11 62576067 62576067 single base substitution T A upstream_gene_variant ESAD-UK 11 62577506 62577506 single base substitution G A upstream_gene_variant ESAD-UK 11 62578756 62578756 single base substitution T G upstream_gene_variant ESCA-CN 11 62563616 62563616 single base substitution G A 3_prime_UTR_variant ESCA-CN 11 62563616 62563616 single base substitution G A downstream_gene_variant ESCA-CN 11 62563616 62563616 single base substitution G A exon_variant ESCA-CN 11 62563616 62563616 single base substitution G A synonymous_variant N461N 1383C>T ESCA-CN 11 62563616 62563616 single base substitution G A synonymous_variant N504N 1512C>T ESCA-CN 11 62563616 62563616 single base substitution G A upstream_gene_variant GBM-US 11 62561731 62561731 single base substitution T C downstream_gene_variant GBM-US 11 62561731 62561731 single base substitution T C missense_variant K587E 1759A>G GBM-US 11 62561731 62561731 single base substitution T C missense_variant K91E 271A>G GBM-US 11 62561731 62561731 single base substitution T C splice_region_variant KIRC-US 11 62557433 62557433 single base substitution A G downstream_gene_variant KIRC-US 11 62569079 62569079 single base substitution C G downstream_gene_variant KIRC-US 11 62569079 62569079 single base substitution C G intron_variant KIRC-US 11 62569079 62569079 single base substitution C G missense_variant G222R 664G>C KIRC-US 11 62569079 62569079 single base substitution C G missense_variant G265R 793G>C KIRC-US 11 62569079 62569079 single base substitution C G missense_variant G85R 253G>C KIRC-US 11 62569079 62569079 single base substitution C G upstream_gene_variant LAML-KR 11 62560570 62560570 single base substitution G T downstream_gene_variant LAML-KR 11 62560570 62560570 single base substitution G T intron_variant LIAD-FR 11 62561816 62561816 single base substitution G C 3_prime_UTR_variant LIAD-FR 11 62561816 62561816 single base substitution G C downstream_gene_variant LIAD-FR 11 62561816 62561816 single base substitution G C exon_variant LIAD-FR 11 62561816 62561816 single base substitution G C missense_variant S558R 1674C>G LIAD-FR 11 62561816 62561816 single base substitution G C missense_variant S601R 1803C>G LIAD-FR 11 62561816 62561816 single base substitution G C missense_variant S62R 186C>G LICA-CN 11 62556565 62556565 single base substitution G A downstream_gene_variant LICA-FR 11 62559154 62559154 single base substitution T C downstream_gene_variant LICA-FR 11 62561816 62561816 single base substitution G C 3_prime_UTR_variant LICA-FR 11 62561816 62561816 single base substitution G C downstream_gene_variant LICA-FR 11 62561816 62561816 single base substitution G C exon_variant LICA-FR 11 62561816 62561816 single base substitution G C missense_variant S558R 1674C>G LICA-FR 11 62561816 62561816 single base substitution G C missense_variant S601R 1803C>G LICA-FR 11 62561816 62561816 single base substitution G C missense_variant S62R 186C>G LIHC-US 11 62560160 62560160 single base substitution T A 3_prime_UTR_variant LIHC-US 11 62560160 62560160 single base substitution T A downstream_gene_variant LIHC-US 11 62560160 62560160 single base substitution T A exon_variant LIHC-US 11 62560160 62560160 single base substitution T A missense_variant N592Y 1774A>T LIHC-US 11 62560160 62560160 single base substitution T A missense_variant N96Y 286A>T LIHC-US 11 62566040 62566040 single base substitution G C 3_prime_UTR_variant LIHC-US 11 62566040 62566040 single base substitution G C downstream_gene_variant LIHC-US 11 62566040 62566040 single base substitution G C exon_variant LIHC-US 11 62566040 62566040 single base substitution G C intron_variant LIHC-US 11 62566040 62566040 single base substitution G C missense_variant R342G 1024C>G LIHC-US 11 62566040 62566040 single base substitution G C missense_variant R385G 1153C>G LIHC-US 11 62566040 62566040 single base substitution G C upstream_gene_variant LIHC-US 11 62571039 62571039 single base substitution G T exon_variant LIHC-US 11 62571039 62571039 single base substitution G T intron_variant LIHC-US 11 62571039 62571039 single base substitution G T missense_variant P117H 350C>A LIHC-US 11 62571039 62571039 single base substitution G T missense_variant P14H 41C>A LIHC-US 11 62571039 62571039 single base substitution G T missense_variant P74H 221C>A LIHC-US 11 62571039 62571039 single base substitution G T upstream_gene_variant LINC-JP 11 62557795 62557795 single base substitution A T downstream_gene_variant LINC-JP 11 62559272 62559272 single base substitution T A downstream_gene_variant LINC-JP 11 62561209 62561209 single base substitution A T downstream_gene_variant LINC-JP 11 62561209 62561209 single base substitution A T intron_variant LINC-JP 11 62563573 62563573 single base substitution C T 3_prime_UTR_variant LINC-JP 11 62563573 62563573 single base substitution C T downstream_gene_variant LINC-JP 11 62563573 62563573 single base substitution C T exon_variant LINC-JP 11 62563573 62563573 single base substitution C T missense_variant V476I 1426G>A LINC-JP 11 62563573 62563573 single base substitution C T missense_variant V519I 1555G>A LINC-JP 11 62563573 62563573 single base substitution C T upstream_gene_variant LINC-JP 11 62564556 62564556 single base substitution C A downstream_gene_variant LINC-JP 11 62564556 62564556 single base substitution C A intron_variant LINC-JP 11 62564556 62564556 single base substitution C A upstream_gene_variant LINC-JP 11 62570674 62570674 single base substitution C T downstream_gene_variant LINC-JP 11 62570674 62570674 single base substitution C T intron_variant LINC-JP 11 62570674 62570674 single base substitution C T upstream_gene_variant LINC-JP 11 62571673 62571673 single base substitution G A intron_variant LINC-JP 11 62571673 62571673 single base substitution G A missense_variant S13L 38C>T LINC-JP 11 62571673 62571673 single base substitution G A upstream_gene_variant LIRI-JP 11 62557222 62557222 single base substitution G A downstream_gene_variant LIRI-JP 11 62559231 62559231 single base substitution G A downstream_gene_variant LIRI-JP 11 62560548 62560548 single base substitution T A downstream_gene_variant LIRI-JP 11 62560548 62560548 single base substitution T A intron_variant LIRI-JP 11 62561883 62561883 single base substitution A G 3_prime_UTR_variant LIRI-JP 11 62561883 62561883 single base substitution A G downstream_gene_variant LIRI-JP 11 62561883 62561883 single base substitution A G exon_variant LIRI-JP 11 62561883 62561883 single base substitution A G intron_variant LIRI-JP 11 62561883 62561883 single base substitution A G missense_variant V536A 1607T>C LIRI-JP 11 62561883 62561883 single base substitution A G missense_variant V579A 1736T>C LIRI-JP 11 62562670 62562670 single base substitution C A downstream_gene_variant LIRI-JP 11 62562670 62562670 single base substitution C A exon_variant LIRI-JP 11 62562670 62562670 single base substitution C A intron_variant LIRI-JP 11 62562670 62562670 single base substitution C A upstream_gene_variant LIRI-JP 11 62564662 62564662 single base substitution G T 3_prime_UTR_variant LIRI-JP 11 62564662 62564662 single base substitution G T downstream_gene_variant LIRI-JP 11 62564662 62564662 single base substitution G T exon_variant LIRI-JP 11 62564662 62564662 single base substitution G T missense_variant L391M 1171C>A LIRI-JP 11 62564662 62564662 single base substitution G T missense_variant L434M 1300C>A LIRI-JP 11 62564662 62564662 single base substitution G T upstream_gene_variant LIRI-JP 11 62564798 62564798 single base substitution G A 3_prime_UTR_variant LIRI-JP 11 62564798 62564798 single base substitution G A downstream_gene_variant LIRI-JP 11 62564798 62564798 single base substitution G A exon_variant LIRI-JP 11 62564798 62564798 single base substitution G A missense_variant P372S 1114C>T LIRI-JP 11 62564798 62564798 single base substitution G A missense_variant P415S 1243C>T LIRI-JP 11 62564798 62564798 single base substitution G A upstream_gene_variant LIRI-JP 11 62565262 62565262 single base substitution G C downstream_gene_variant LIRI-JP 11 62565262 62565262 single base substitution G C intron_variant LIRI-JP 11 62565262 62565262 single base substitution G C upstream_gene_variant LIRI-JP 11 62565451 62565451 single base substitution A G downstream_gene_variant LIRI-JP 11 62565451 62565451 single base substitution A G intron_variant LIRI-JP 11 62565451 62565451 single base substitution A G upstream_gene_variant LIRI-JP 11 62566375 62566375 single base substitution G A 3_prime_UTR_variant LIRI-JP 11 62566375 62566375 single base substitution G A downstream_gene_variant LIRI-JP 11 62566375 62566375 single base substitution G A exon_variant LIRI-JP 11 62566375 62566375 single base substitution G A intron_variant LIRI-JP 11 62566375 62566375 single base substitution G A upstream_gene_variant LIRI-JP 11 62570498 62570500 deletion of <=200bp AGG - downstream_gene_variant LIRI-JP 11 62570498 62570500 deletion of <=200bp AGG - intron_variant LIRI-JP 11 62570498 62570500 deletion of <=200bp AGG - upstream_gene_variant LIRI-JP 11 62570603 62570603 single base substitution C T downstream_gene_variant LIRI-JP 11 62570603 62570603 single base substitution C T intron_variant LIRI-JP 11 62570603 62570603 single base substitution C T upstream_gene_variant LIRI-JP 11 62576214 62576214 single base substitution T C upstream_gene_variant LIRI-JP 11 62577494 62577494 single base substitution A C upstream_gene_variant LUSC-KR 11 62554846 62554846 single base substitution T A downstream_gene_variant LUSC-KR 11 62555006 62555006 single base substitution C A downstream_gene_variant LUSC-KR 11 62559267 62559267 single base substitution A T downstream_gene_variant LUSC-KR 11 62559272 62559272 single base substitution T A downstream_gene_variant LUSC-KR 11 62560570 62560570 single base substitution G T downstream_gene_variant LUSC-KR 11 62560570 62560570 single base substitution G T intron_variant LUSC-KR 11 62564556 62564556 single base substitution C A downstream_gene_variant LUSC-KR 11 62564556 62564556 single base substitution C A intron_variant LUSC-KR 11 62564556 62564556 single base substitution C A upstream_gene_variant LUSC-KR 11 62564561 62564561 single base substitution C A downstream_gene_variant LUSC-KR 11 62564561 62564561 single base substitution C A intron_variant LUSC-KR 11 62564561 62564561 single base substitution C A upstream_gene_variant LUSC-KR 11 62572994 62572994 single base substitution C A 5_prime_UTR_premature_start_codon_gain_variant LUSC-KR 11 62572994 62572994 single base substitution C A upstream_gene_variant LUSC-KR 11 62573910 62573910 single base substitution C T upstream_gene_variant LUSC-KR 11 62577613 62577613 single base substitution T G upstream_gene_variant LUSC-US 11 62554633 62554633 single base substitution C G downstream_gene_variant LUSC-US 11 62568576 62568576 single base substitution G C downstream_gene_variant LUSC-US 11 62568576 62568576 single base substitution G C intron_variant LUSC-US 11 62568576 62568576 single base substitution G C missense_variant S162C 485C>G LUSC-US 11 62568576 62568576 single base substitution G C missense_variant S299C 896C>G LUSC-US 11 62568576 62568576 single base substitution G C missense_variant S342C 1025C>G LUSC-US 11 62568576 62568576 single base substitution G C upstream_gene_variant LUSC-US 11 62568599 62568599 single base substitution G T downstream_gene_variant LUSC-US 11 62568599 62568599 single base substitution G T intron_variant LUSC-US 11 62568599 62568599 single base substitution G T synonymous_variant P154P 462C>A LUSC-US 11 62568599 62568599 single base substitution G T synonymous_variant P291P 873C>A LUSC-US 11 62568599 62568599 single base substitution G T synonymous_variant P334P 1002C>A LUSC-US 11 62568599 62568599 single base substitution G T upstream_gene_variant LUSC-US 11 62569222 62569222 single base substitution C T downstream_gene_variant LUSC-US 11 62569222 62569222 single base substitution C T intron_variant LUSC-US 11 62569222 62569222 single base substitution C T missense_variant E210K 628G>A LUSC-US 11 62569222 62569222 single base substitution C T missense_variant E253K 757G>A LUSC-US 11 62569222 62569222 single base substitution C T missense_variant E73K 217G>A LUSC-US 11 62569222 62569222 single base substitution C T upstream_gene_variant MALY-DE 11 62554890 62554890 single base substitution G T downstream_gene_variant MALY-DE 11 62558433 62558433 single base substitution C G downstream_gene_variant MALY-DE 11 62561100 62561100 single base substitution G T downstream_gene_variant MALY-DE 11 62561100 62561100 single base substitution G T intron_variant MALY-DE 11 62564577 62564577 single base substitution A G downstream_gene_variant MALY-DE 11 62564577 62564577 single base substitution A G intron_variant MALY-DE 11 62564577 62564577 single base substitution A G upstream_gene_variant MALY-DE 11 62566649 62566649 single base substitution G C 3_prime_UTR_variant MALY-DE 11 62566649 62566649 single base substitution G C downstream_gene_variant MALY-DE 11 62566649 62566649 single base substitution G C exon_variant MALY-DE 11 62566649 62566649 single base substitution G C intron_variant MALY-DE 11 62566649 62566649 single base substitution G C upstream_gene_variant MALY-DE 11 62568074 62568074 single base substitution T G downstream_gene_variant MALY-DE 11 62568074 62568074 single base substitution T G intron_variant MALY-DE 11 62568074 62568074 single base substitution T G upstream_gene_variant MALY-DE 11 62569419 62569419 single base substitution G A downstream_gene_variant MALY-DE 11 62569419 62569419 single base substitution G A intron_variant MALY-DE 11 62569419 62569419 single base substitution G A stop_gained R185* 553C>T MALY-DE 11 62569419 62569419 single base substitution G A stop_gained R228* 682C>T MALY-DE 11 62569419 62569419 single base substitution G A stop_gained R48* 142C>T MALY-DE 11 62569419 62569419 single base substitution G A upstream_gene_variant MALY-DE 11 62571933 62571933 single base substitution T C intron_variant MALY-DE 11 62571933 62571933 single base substitution T C upstream_gene_variant MALY-DE 11 62572119 62572119 single base substitution A C intron_variant MALY-DE 11 62572119 62572119 single base substitution A C upstream_gene_variant MALY-DE 11 62576564 62576564 single base substitution T C upstream_gene_variant MALY-DE 11 62577196 62577196 single base substitution G C upstream_gene_variant MELA-AU 11 62554633 62554633 single base substitution C T downstream_gene_variant MELA-AU 11 62554712 62554712 single base substitution A T downstream_gene_variant MELA-AU 11 62554787 62554787 single base substitution C T downstream_gene_variant MELA-AU 11 62554889 62554889 single base substitution G A downstream_gene_variant MELA-AU 11 62556735 62556735 single base substitution C T downstream_gene_variant MELA-AU 11 62557107 62557107 single base substitution C T downstream_gene_variant MELA-AU 11 62557441 62557442 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 11 62559514 62559514 single base substitution C T downstream_gene_variant MELA-AU 11 62559909 62559909 single base substitution C A 3_prime_UTR_variant MELA-AU 11 62559909 62559909 single base substitution C A downstream_gene_variant MELA-AU 11 62559909 62559909 single base substitution C A exon_variant MELA-AU 11 62561210 62561210 single base substitution C T downstream_gene_variant MELA-AU 11 62561210 62561210 single base substitution C T intron_variant MELA-AU 11 62561516 62561516 single base substitution A T downstream_gene_variant MELA-AU 11 62561516 62561516 single base substitution A T intron_variant MELA-AU 11 62562004 62562005 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 11 62562004 62562005 multiple base substitution (>=2bp and <=200bp) GG AA exon_variant MELA-AU 11 62562004 62562005 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 11 62563281 62563281 single base substitution G A downstream_gene_variant MELA-AU 11 62563281 62563281 single base substitution G A intron_variant MELA-AU 11 62563281 62563281 single base substitution G A upstream_gene_variant MELA-AU 11 62563806 62563806 single base substitution G A 3_prime_UTR_variant MELA-AU 11 62563806 62563806 single base substitution G A downstream_gene_variant MELA-AU 11 62563806 62563806 single base substitution G A exon_variant MELA-AU 11 62563806 62563806 single base substitution G A missense_variant A433V 1298C>T MELA-AU 11 62563806 62563806 single base substitution G A missense_variant A476V 1427C>T MELA-AU 11 62563806 62563806 single base substitution G A upstream_gene_variant MELA-AU 11 62563849 62563849 single base substitution C T downstream_gene_variant MELA-AU 11 62563849 62563849 single base substitution C T intron_variant MELA-AU 11 62563849 62563849 single base substitution C T upstream_gene_variant MELA-AU 11 62564046 62564046 single base substitution G A downstream_gene_variant MELA-AU 11 62564046 62564046 single base substitution G A intron_variant MELA-AU 11 62564046 62564046 single base substitution G A splice_region_variant MELA-AU 11 62564046 62564046 single base substitution G A upstream_gene_variant MELA-AU 11 62564115 62564115 single base substitution G A downstream_gene_variant MELA-AU 11 62564115 62564115 single base substitution G A intron_variant MELA-AU 11 62564115 62564115 single base substitution G A upstream_gene_variant MELA-AU 11 62564225 62564225 single base substitution G A downstream_gene_variant MELA-AU 11 62564225 62564225 single base substitution G A intron_variant MELA-AU 11 62564225 62564225 single base substitution G A upstream_gene_variant MELA-AU 11 62564630 62564630 single base substitution G A downstream_gene_variant MELA-AU 11 62564630 62564630 single base substitution G A intron_variant MELA-AU 11 62564630 62564630 single base substitution G A upstream_gene_variant MELA-AU 11 62564646 62564646 single base substitution G A downstream_gene_variant MELA-AU 11 62564646 62564646 single base substitution G A intron_variant MELA-AU 11 62564646 62564646 single base substitution G A upstream_gene_variant MELA-AU 11 62565200 62565200 single base substitution G A downstream_gene_variant MELA-AU 11 62565200 62565200 single base substitution G A intron_variant MELA-AU 11 62565200 62565200 single base substitution G A upstream_gene_variant MELA-AU 11 62565754 62565754 single base substitution G C downstream_gene_variant MELA-AU 11 62565754 62565754 single base substitution G C intron_variant MELA-AU 11 62565754 62565754 single base substitution G C upstream_gene_variant MELA-AU 11 62565953 62565953 single base substitution G A downstream_gene_variant MELA-AU 11 62565953 62565953 single base substitution G A intron_variant MELA-AU 11 62565953 62565953 single base substitution G A upstream_gene_variant MELA-AU 11 62566220 62566220 single base substitution G A 3_prime_UTR_variant MELA-AU 11 62566220 62566220 single base substitution G A downstream_gene_variant MELA-AU 11 62566220 62566220 single base substitution G A intron_variant MELA-AU 11 62566220 62566220 single base substitution G A upstream_gene_variant MELA-AU 11 62566380 62566380 single base substitution G A 3_prime_UTR_variant MELA-AU 11 62566380 62566380 single base substitution G A downstream_gene_variant MELA-AU 11 62566380 62566380 single base substitution G A exon_variant MELA-AU 11 62566380 62566380 single base substitution G A intron_variant MELA-AU 11 62566380 62566380 single base substitution G A upstream_gene_variant MELA-AU 11 62566552 62566552 single base substitution G A 3_prime_UTR_variant MELA-AU 11 62566552 62566552 single base substitution G A downstream_gene_variant MELA-AU 11 62566552 62566552 single base substitution G A exon_variant MELA-AU 11 62566552 62566552 single base substitution G A intron_variant MELA-AU 11 62566552 62566552 single base substitution G A upstream_gene_variant MELA-AU 11 62566697 62566697 single base substitution G A 3_prime_UTR_variant MELA-AU 11 62566697 62566697 single base substitution G A downstream_gene_variant MELA-AU 11 62566697 62566697 single base substitution G A exon_variant MELA-AU 11 62566697 62566697 single base substitution G A intron_variant MELA-AU 11 62566697 62566697 single base substitution G A upstream_gene_variant MELA-AU 11 62567932 62567932 single base substitution C T downstream_gene_variant MELA-AU 11 62567932 62567932 single base substitution C T exon_variant MELA-AU 11 62567932 62567932 single base substitution C T intron_variant MELA-AU 11 62567932 62567932 single base substitution C T synonymous_variant K174K 522G>A MELA-AU 11 62567932 62567932 single base substitution C T synonymous_variant K311K 933G>A MELA-AU 11 62567932 62567932 single base substitution C T synonymous_variant K354K 1062G>A MELA-AU 11 62567932 62567932 single base substitution C T upstream_gene_variant MELA-AU 11 62568580 62568580 single base substitution G A downstream_gene_variant MELA-AU 11 62568580 62568580 single base substitution G A intron_variant MELA-AU 11 62568580 62568580 single base substitution G A missense_variant L161F 481C>T MELA-AU 11 62568580 62568580 single base substitution G A missense_variant L298F 892C>T MELA-AU 11 62568580 62568580 single base substitution G A missense_variant L341F 1021C>T MELA-AU 11 62568580 62568580 single base substitution G A upstream_gene_variant MELA-AU 11 62568813 62568813 single base substitution C T downstream_gene_variant MELA-AU 11 62568813 62568813 single base substitution C T exon_variant MELA-AU 11 62568813 62568813 single base substitution C T intron_variant MELA-AU 11 62568813 62568813 single base substitution C T synonymous_variant E125E 375G>A MELA-AU 11 62568813 62568813 single base substitution C T synonymous_variant E262E 786G>A MELA-AU 11 62568813 62568813 single base substitution C T synonymous_variant E305E 915G>A MELA-AU 11 62568813 62568813 single base substitution C T upstream_gene_variant MELA-AU 11 62569584 62569584 single base substitution G T downstream_gene_variant MELA-AU 11 62569584 62569584 single base substitution G T intron_variant MELA-AU 11 62569584 62569584 single base substitution G T upstream_gene_variant MELA-AU 11 62569609 62569609 single base substitution C T downstream_gene_variant MELA-AU 11 62569609 62569609 single base substitution C T intron_variant MELA-AU 11 62569609 62569609 single base substitution C T upstream_gene_variant MELA-AU 11 62569761 62569761 single base substitution G A downstream_gene_variant MELA-AU 11 62569761 62569761 single base substitution G A intron_variant MELA-AU 11 62569761 62569761 single base substitution G A upstream_gene_variant MELA-AU 11 62569844 62569844 single base substitution G A downstream_gene_variant MELA-AU 11 62569844 62569844 single base substitution G A intron_variant MELA-AU 11 62569844 62569844 single base substitution G A upstream_gene_variant MELA-AU 11 62570386 62570386 single base substitution A G downstream_gene_variant MELA-AU 11 62570386 62570386 single base substitution A G intron_variant MELA-AU 11 62570386 62570386 single base substitution A G upstream_gene_variant MELA-AU 11 62571019 62571019 single base substitution G A 3_prime_UTR_variant MELA-AU 11 62571019 62571019 single base substitution G A downstream_gene_variant MELA-AU 11 62571019 62571019 single base substitution G A intron_variant MELA-AU 11 62571019 62571019 single base substitution G A missense_variant R124C 370C>T MELA-AU 11 62571019 62571019 single base substitution G A missense_variant R21C 61C>T MELA-AU 11 62571019 62571019 single base substitution G A missense_variant R81C 241C>T MELA-AU 11 62571019 62571019 single base substitution G A upstream_gene_variant MELA-AU 11 62572994 62572994 single base substitution C T 5_prime_UTR_variant MELA-AU 11 62572994 62572994 single base substitution C T upstream_gene_variant MELA-AU 11 62573046 62573046 single base substitution C T 5_prime_UTR_variant MELA-AU 11 62573046 62573046 single base substitution C T upstream_gene_variant MELA-AU 11 62573073 62573073 single base substitution C T 5_prime_UTR_variant MELA-AU 11 62573073 62573073 single base substitution C T upstream_gene_variant MELA-AU 11 62573441 62573441 single base substitution C T intron_variant MELA-AU 11 62573441 62573441 single base substitution C T upstream_gene_variant MELA-AU 11 62573642 62573642 single base substitution G A intron_variant MELA-AU 11 62573642 62573642 single base substitution G A upstream_gene_variant MELA-AU 11 62574340 62574340 single base substitution C A upstream_gene_variant MELA-AU 11 62575112 62575112 single base substitution G A upstream_gene_variant MELA-AU 11 62575901 62575901 single base substitution G A upstream_gene_variant MELA-AU 11 62575905 62575905 single base substitution G A upstream_gene_variant MELA-AU 11 62575933 62575933 single base substitution A T upstream_gene_variant MELA-AU 11 62576436 62576436 single base substitution G A upstream_gene_variant MELA-AU 11 62577106 62577106 single base substitution A C upstream_gene_variant MELA-AU 11 62577823 62577823 single base substitution G A upstream_gene_variant MELA-AU 11 62578040 62578040 single base substitution G A upstream_gene_variant MELA-AU 11 62578232 62578232 single base substitution C T upstream_gene_variant ORCA-IN 11 62563635 62563635 single base substitution A G 3_prime_UTR_variant ORCA-IN 11 62563635 62563635 single base substitution A G downstream_gene_variant ORCA-IN 11 62563635 62563635 single base substitution A G exon_variant ORCA-IN 11 62563635 62563635 single base substitution A G missense_variant L455P 1364T>C ORCA-IN 11 62563635 62563635 single base substitution A G missense_variant L498P 1493T>C ORCA-IN 11 62563635 62563635 single base substitution A G upstream_gene_variant ORCA-IN 11 62570850 62570850 single base substitution T A downstream_gene_variant ORCA-IN 11 62570850 62570850 single base substitution T A intron_variant ORCA-IN 11 62570850 62570850 single base substitution T A upstream_gene_variant ORCA-IN 11 62575050 62575050 single base substitution G A upstream_gene_variant ORCA-IN 11 62576140 62576140 single base substitution G A upstream_gene_variant ORCA-IN 11 62577507 62577507 single base substitution G A upstream_gene_variant OV-AU 11 62555023 62555023 single base substitution G A downstream_gene_variant OV-AU 11 62557904 62557904 single base substitution T G downstream_gene_variant OV-AU 11 62558918 62558918 single base substitution A G downstream_gene_variant OV-AU 11 62566871 62566871 single base substitution G C 3_prime_UTR_variant OV-AU 11 62566871 62566871 single base substitution G C downstream_gene_variant OV-AU 11 62566871 62566871 single base substitution G C intron_variant OV-AU 11 62566871 62566871 single base substitution G C upstream_gene_variant OV-AU 11 62571935 62571935 single base substitution C G intron_variant OV-AU 11 62571935 62571935 single base substitution C G upstream_gene_variant OV-AU 11 62572890 62572890 single base substitution T C 5_prime_UTR_variant OV-AU 11 62572890 62572890 single base substitution T C exon_variant OV-AU 11 62572890 62572890 single base substitution T C upstream_gene_variant OV-AU 11 62576928 62576928 single base substitution C T upstream_gene_variant PACA-AU 11 62554830 62554830 single base substitution C T downstream_gene_variant PACA-AU 11 62555174 62555174 single base substitution C A downstream_gene_variant PACA-AU 11 62556878 62556878 single base substitution C G downstream_gene_variant PACA-AU 11 62561746 62561746 single base substitution G A 3_prime_UTR_variant PACA-AU 11 62561746 62561746 single base substitution G A downstream_gene_variant PACA-AU 11 62561746 62561746 single base substitution G A exon_variant PACA-AU 11 62561746 62561746 single base substitution G A missense_variant L582F 1744C>T PACA-AU 11 62561746 62561746 single base substitution G A missense_variant L86F 256C>T PACA-AU 11 62562485 62562485 single base substitution A G downstream_gene_variant PACA-AU 11 62562485 62562485 single base substitution A G exon_variant PACA-AU 11 62562485 62562485 single base substitution A G intron_variant PACA-AU 11 62562485 62562485 single base substitution A G splice_region_variant PACA-AU 11 62562485 62562485 single base substitution A G upstream_gene_variant PACA-AU 11 62562878 62562878 single base substitution A T downstream_gene_variant PACA-AU 11 62562878 62562878 single base substitution A T intron_variant PACA-AU 11 62562878 62562878 single base substitution A T upstream_gene_variant PACA-AU 11 62567870 62567870 single base substitution C T downstream_gene_variant PACA-AU 11 62567870 62567870 single base substitution C T exon_variant PACA-AU 11 62567870 62567870 single base substitution C T intron_variant PACA-AU 11 62567870 62567870 single base substitution C T missense_variant R195Q 584G>A PACA-AU 11 62567870 62567870 single base substitution C T missense_variant R332Q 995G>A PACA-AU 11 62567870 62567870 single base substitution C T missense_variant R375Q 1124G>A PACA-AU 11 62567870 62567870 single base substitution C T upstream_gene_variant PACA-AU 11 62569218 62569226 deletion of <=200bp TGTTCTACT - disruptive_inframe_deletion QVEQ208Q PACA-AU 11 62569218 62569226 deletion of <=200bp TGTTCTACT - disruptive_inframe_deletion QVEQ251Q PACA-AU 11 62569218 62569226 deletion of <=200bp TGTTCTACT - disruptive_inframe_deletion QVEQ71Q PACA-AU 11 62569218 62569226 deletion of <=200bp TGTTCTACT - downstream_gene_variant PACA-AU 11 62569218 62569226 deletion of <=200bp TGTTCTACT - intron_variant PACA-AU 11 62569218 62569226 deletion of <=200bp TGTTCTACT - upstream_gene_variant PACA-AU 11 62570651 62570651 single base substitution C A downstream_gene_variant PACA-AU 11 62570651 62570651 single base substitution C A intron_variant PACA-AU 11 62570651 62570651 single base substitution C A upstream_gene_variant PACA-AU 11 62571540 62571540 single base substitution G C 5_prime_UTR_premature_start_codon_gain_variant PACA-AU 11 62571540 62571540 single base substitution G C intron_variant PACA-AU 11 62575909 62575909 single base substitution A G upstream_gene_variant PACA-AU 11 62577547 62577548 deletion of <=200bp AC - upstream_gene_variant PACA-CA 11 62554681 62554681 single base substitution C A downstream_gene_variant PACA-CA 11 62560174 62560174 single base substitution C A downstream_gene_variant PACA-CA 11 62560174 62560174 single base substitution C A splice_acceptor_variant PACA-CA 11 62564786 62564786 single base substitution C A downstream_gene_variant PACA-CA 11 62564786 62564786 single base substitution C A splice_region_variant PACA-CA 11 62564786 62564786 single base substitution C A upstream_gene_variant PACA-CA 11 62564959 62564959 single base substitution C T downstream_gene_variant PACA-CA 11 62564959 62564959 single base substitution C T intron_variant PACA-CA 11 62564959 62564959 single base substitution C T upstream_gene_variant PACA-CA 11 62568437 62568437 single base substitution G T downstream_gene_variant PACA-CA 11 62568437 62568437 single base substitution G T intron_variant PACA-CA 11 62568437 62568437 single base substitution G T upstream_gene_variant PACA-CA 11 62569209 62569209 single base substitution A G downstream_gene_variant PACA-CA 11 62569209 62569209 single base substitution A G intron_variant PACA-CA 11 62569209 62569209 single base substitution A G splice_donor_variant PACA-CA 11 62569209 62569209 single base substitution A G upstream_gene_variant PACA-CA 11 62571378 62571378 single base substitution C G 5_prime_UTR_premature_start_codon_gain_variant PACA-CA 11 62571378 62571378 single base substitution C G exon_variant PACA-CA 11 62571378 62571378 single base substitution C G intron_variant PACA-CA 11 62571378 62571378 single base substitution C G missense_variant G34A 101G>C PACA-CA 11 62571378 62571378 single base substitution C G missense_variant G77A 230G>C PBCA-DE 11 62568783 62568783 single base substitution C A downstream_gene_variant PBCA-DE 11 62568783 62568783 single base substitution C A intron_variant PBCA-DE 11 62568783 62568783 single base substitution C A upstream_gene_variant PRAD-CA 11 62576239 62576239 single base substitution T C upstream_gene_variant PRAD-UK 11 62578709 62578709 single base substitution C G upstream_gene_variant PRAD-US 11 62559255 62559255 deletion of <=200bp G - downstream_gene_variant READ-US 11 62569733 62569733 single base substitution C T downstream_gene_variant READ-US 11 62569733 62569733 single base substitution C T intron_variant READ-US 11 62569733 62569733 single base substitution C T splice_acceptor_variant READ-US 11 62569733 62569733 single base substitution C T upstream_gene_variant RECA-EU 11 62555496 62555496 single base substitution C T downstream_gene_variant RECA-EU 11 62558201 62558201 single base substitution G C downstream_gene_variant RECA-EU 11 62560818 62560818 single base substitution G A downstream_gene_variant RECA-EU 11 62560818 62560818 single base substitution G A intron_variant RECA-EU 11 62565755 62565755 single base substitution C T downstream_gene_variant RECA-EU 11 62565755 62565755 single base substitution C T intron_variant RECA-EU 11 62565755 62565755 single base substitution C T upstream_gene_variant RECA-EU 11 62570198 62570198 single base substitution T G downstream_gene_variant RECA-EU 11 62570198 62570198 single base substitution T G intron_variant RECA-EU 11 62570198 62570198 single base substitution T G upstream_gene_variant SKCA-BR 11 62555019 62555019 single base substitution T G downstream_gene_variant SKCA-BR 11 62555034 62555034 single base substitution A G downstream_gene_variant SKCA-BR 11 62560547 62560547 single base substitution C T downstream_gene_variant SKCA-BR 11 62560547 62560547 single base substitution C T intron_variant SKCA-BR 11 62568198 62568198 single base substitution C T downstream_gene_variant SKCA-BR 11 62568198 62568198 single base substitution C T intron_variant SKCA-BR 11 62568198 62568198 single base substitution C T upstream_gene_variant SKCA-BR 11 62569098 62569098 single base substitution G A downstream_gene_variant SKCA-BR 11 62569098 62569098 single base substitution G A intron_variant SKCA-BR 11 62569098 62569098 single base substitution G A synonymous_variant I215I 645C>T SKCA-BR 11 62569098 62569098 single base substitution G A synonymous_variant I258I 774C>T SKCA-BR 11 62569098 62569098 single base substitution G A synonymous_variant I78I 234C>T SKCA-BR 11 62569098 62569098 single base substitution G A upstream_gene_variant SKCA-BR 11 62569761 62569761 single base substitution G A downstream_gene_variant SKCA-BR 11 62569761 62569761 single base substitution G A intron_variant SKCA-BR 11 62569761 62569761 single base substitution G A upstream_gene_variant SKCA-BR 11 62570583 62570583 single base substitution G A downstream_gene_variant SKCA-BR 11 62570583 62570583 single base substitution G A intron_variant SKCA-BR 11 62570583 62570583 single base substitution G A upstream_gene_variant SKCA-BR 11 62572813 62572813 single base substitution T C 5_prime_UTR_variant SKCA-BR 11 62572813 62572813 single base substitution T C exon_variant SKCA-BR 11 62572813 62572813 single base substitution T C missense_variant K6E 16A>G SKCA-BR 11 62572813 62572813 single base substitution T C upstream_gene_variant SKCA-BR 11 62573516 62573516 single base substitution T C intron_variant SKCA-BR 11 62573516 62573516 single base substitution T C upstream_gene_variant SKCA-BR 11 62573522 62573522 single base substitution A C intron_variant SKCA-BR 11 62573522 62573522 single base substitution A C upstream_gene_variant SKCA-BR 11 62576747 62576747 single base substitution G A upstream_gene_variant SKCM-US 11 62554665 62554665 single base substitution G A downstream_gene_variant SKCM-US 11 62556590 62556590 single base substitution C T downstream_gene_variant SKCM-US 11 62558255 62558255 single base substitution G A downstream_gene_variant SKCM-US 11 62562413 62562413 single base substitution T A 3_prime_UTR_variant SKCM-US 11 62562413 62562413 single base substitution T A downstream_gene_variant SKCM-US 11 62562413 62562413 single base substitution T A exon_variant SKCM-US 11 62562413 62562413 single base substitution T A missense_variant N42I 125A>T SKCM-US 11 62562413 62562413 single base substitution T A missense_variant N524I 1571A>T SKCM-US 11 62562413 62562413 single base substitution T A missense_variant N567I 1700A>T SKCM-US 11 62562413 62562413 single base substitution T A upstream_gene_variant SKCM-US 11 62564692 62564692 single base substitution C T 3_prime_UTR_variant SKCM-US 11 62564692 62564692 single base substitution C T downstream_gene_variant SKCM-US 11 62564692 62564692 single base substitution C T exon_variant SKCM-US 11 62564692 62564692 single base substitution C T missense_variant E381K 1141G>A SKCM-US 11 62564692 62564692 single base substitution C T missense_variant E424K 1270G>A SKCM-US 11 62564692 62564692 single base substitution C T upstream_gene_variant SKCM-US 11 62566040 62566040 single base substitution G A 3_prime_UTR_variant SKCM-US 11 62566040 62566040 single base substitution G A downstream_gene_variant SKCM-US 11 62566040 62566040 single base substitution G A exon_variant SKCM-US 11 62566040 62566040 single base substitution G A intron_variant SKCM-US 11 62566040 62566040 single base substitution G A missense_variant R342C 1024C>T SKCM-US 11 62566040 62566040 single base substitution G A missense_variant R385C 1153C>T SKCM-US 11 62566040 62566040 single base substitution G A upstream_gene_variant SKCM-US 11 62568807 62568807 single base substitution G A downstream_gene_variant SKCM-US 11 62568807 62568807 single base substitution G A exon_variant SKCM-US 11 62568807 62568807 single base substitution G A intron_variant SKCM-US 11 62568807 62568807 single base substitution G A synonymous_variant I127I 381C>T SKCM-US 11 62568807 62568807 single base substitution G A synonymous_variant I264I 792C>T SKCM-US 11 62568807 62568807 single base substitution G A synonymous_variant I307I 921C>T SKCM-US 11 62568807 62568807 single base substitution G A upstream_gene_variant SKCM-US 11 62569098 62569098 single base substitution G A downstream_gene_variant SKCM-US 11 62569098 62569098 single base substitution G A intron_variant SKCM-US 11 62569098 62569098 single base substitution G A synonymous_variant I215I 645C>T SKCM-US 11 62569098 62569098 single base substitution G A synonymous_variant I258I 774C>T SKCM-US 11 62569098 62569098 single base substitution G A synonymous_variant I78I 234C>T SKCM-US 11 62569098 62569098 single base substitution G A upstream_gene_variant SKCM-US 11 62569260 62569260 single base substitution G A downstream_gene_variant SKCM-US 11 62569260 62569260 single base substitution G A intron_variant SKCM-US 11 62569260 62569260 single base substitution G A missense_variant P197L 590C>T SKCM-US 11 62569260 62569260 single base substitution G A missense_variant P240L 719C>T SKCM-US 11 62569260 62569260 single base substitution G A missense_variant P60L 179C>T SKCM-US 11 62569260 62569260 single base substitution G A upstream_gene_variant SKCM-US 11 62569486 62569486 single base substitution G A 3_prime_UTR_variant SKCM-US 11 62569486 62569486 single base substitution G A downstream_gene_variant SKCM-US 11 62569486 62569486 single base substitution G A intron_variant SKCM-US 11 62569486 62569486 single base substitution G A synonymous_variant F102F 306C>T SKCM-US 11 62569486 62569486 single base substitution G A synonymous_variant F162F 486C>T SKCM-US 11 62569486 62569486 single base substitution G A synonymous_variant F205F 615C>T SKCM-US 11 62569486 62569486 single base substitution G A synonymous_variant F25F 75C>T SKCM-US 11 62569486 62569486 single base substitution G A upstream_gene_variant SKCM-US 11 62574950 62574950 single base substitution G A upstream_gene_variant STAD-US 11 62557411 62557411 single base substitution C T downstream_gene_variant STAD-US 11 62563573 62563573 single base substitution C T 3_prime_UTR_variant STAD-US 11 62563573 62563573 single base substitution C T downstream_gene_variant STAD-US 11 62563573 62563573 single base substitution C T exon_variant STAD-US 11 62563573 62563573 single base substitution C T missense_variant V476I 1426G>A STAD-US 11 62563573 62563573 single base substitution C T missense_variant V519I 1555G>A STAD-US 11 62563573 62563573 single base substitution C T upstream_gene_variant STAD-US 11 62564692 62564692 single base substitution C A 3_prime_UTR_variant STAD-US 11 62564692 62564692 single base substitution C A downstream_gene_variant STAD-US 11 62564692 62564692 single base substitution C A exon_variant STAD-US 11 62564692 62564692 single base substitution C A stop_gained E381* 1141G>T STAD-US 11 62564692 62564692 single base substitution C A stop_gained E424* 1270G>T STAD-US 11 62564692 62564692 single base substitution C A upstream_gene_variant STAD-US 11 62567923 62567923 single base substitution C T downstream_gene_variant STAD-US 11 62567923 62567923 single base substitution C T exon_variant STAD-US 11 62567923 62567923 single base substitution C T intron_variant STAD-US 11 62567923 62567923 single base substitution C T synonymous_variant G177G 531G>A STAD-US 11 62567923 62567923 single base substitution C T synonymous_variant G314G 942G>A STAD-US 11 62567923 62567923 single base substitution C T synonymous_variant G357G 1071G>A STAD-US 11 62567923 62567923 single base substitution C T upstream_gene_variant STAD-US 11 62569046 62569046 single base substitution G A downstream_gene_variant STAD-US 11 62569046 62569046 single base substitution G A intron_variant STAD-US 11 62569046 62569046 single base substitution G A missense_variant R233C 697C>T STAD-US 11 62569046 62569046 single base substitution G A missense_variant R276C 826C>T STAD-US 11 62569046 62569046 single base substitution G A missense_variant R96C 286C>T STAD-US 11 62569046 62569046 single base substitution G A upstream_gene_variant STAD-US 11 62569076 62569076 single base substitution A G downstream_gene_variant STAD-US 11 62569076 62569076 single base substitution A G intron_variant STAD-US 11 62569076 62569076 single base substitution A G missense_variant S223P 667T>C STAD-US 11 62569076 62569076 single base substitution A G missense_variant S266P 796T>C STAD-US 11 62569076 62569076 single base substitution A G missense_variant S86P 256T>C STAD-US 11 62569076 62569076 single base substitution A G upstream_gene_variant STAD-US 11 62569260 62569260 single base substitution G A downstream_gene_variant STAD-US 11 62569260 62569260 single base substitution G A intron_variant STAD-US 11 62569260 62569260 single base substitution G A missense_variant P197L 590C>T STAD-US 11 62569260 62569260 single base substitution G A missense_variant P240L 719C>T STAD-US 11 62569260 62569260 single base substitution G A missense_variant P60L 179C>T STAD-US 11 62569260 62569260 single base substitution G A upstream_gene_variant STAD-US 11 62569485 62569485 single base substitution C T 3_prime_UTR_variant STAD-US 11 62569485 62569485 single base substitution C T downstream_gene_variant STAD-US 11 62569485 62569485 single base substitution C T intron_variant STAD-US 11 62569485 62569485 single base substitution C T missense_variant V103I 307G>A STAD-US 11 62569485 62569485 single base substitution C T missense_variant V163I 487G>A STAD-US 11 62569485 62569485 single base substitution C T missense_variant V206I 616G>A STAD-US 11 62569485 62569485 single base substitution C T missense_variant V26I 76G>A STAD-US 11 62569485 62569485 single base substitution C T upstream_gene_variant STAD-US 11 62569689 62569689 single base substitution A G 3_prime_UTR_variant STAD-US 11 62569689 62569689 single base substitution A G downstream_gene_variant STAD-US 11 62569689 62569689 single base substitution A G exon_variant STAD-US 11 62569689 62569689 single base substitution A G intron_variant STAD-US 11 62569689 62569689 single base substitution A G missense_variant M138T 413T>C STAD-US 11 62569689 62569689 single base substitution A G missense_variant M181T 542T>C STAD-US 11 62569689 62569689 single base substitution A G missense_variant M78T 233T>C STAD-US 11 62569689 62569689 single base substitution A G start_lost M1T 2T>C STAD-US 11 62569689 62569689 single base substitution A G upstream_gene_variant UCEC-US 11 62556623 62556623 single base substitution C T downstream_gene_variant UCEC-US 11 62556810 62556810 single base substitution G A downstream_gene_variant UCEC-US 11 62557503 62557503 single base substitution G A downstream_gene_variant UCEC-US 11 62558156 62558156 single base substitution G T downstream_gene_variant UCEC-US 11 62558172 62558172 single base substitution A C downstream_gene_variant UCEC-US 11 62558182 62558182 single base substitution T C downstream_gene_variant UCEC-US 11 62558184 62558184 single base substitution G A downstream_gene_variant UCEC-US 11 62560123 62560123 single base substitution G A 3_prime_UTR_variant UCEC-US 11 62560123 62560123 single base substitution G A downstream_gene_variant UCEC-US 11 62560123 62560123 single base substitution G A exon_variant UCEC-US 11 62560123 62560123 single base substitution G A missense_variant T108I 323C>T UCEC-US 11 62560123 62560123 single base substitution G A missense_variant T604I 1811C>T UCEC-US 11 62561744 62561744 single base substitution G A 3_prime_UTR_variant UCEC-US 11 62561744 62561744 single base substitution G A downstream_gene_variant UCEC-US 11 62561744 62561744 single base substitution G A exon_variant UCEC-US 11 62561744 62561744 single base substitution G A synonymous_variant L582L 1746C>T UCEC-US 11 62561744 62561744 single base substitution G A synonymous_variant L86L 258C>T UCEC-US 11 62561828 62561828 single base substitution C T 3_prime_UTR_variant UCEC-US 11 62561828 62561828 single base substitution C T downstream_gene_variant UCEC-US 11 62561828 62561828 single base substitution C T exon_variant UCEC-US 11 62561828 62561828 single base substitution C T synonymous_variant T554T 1662G>A UCEC-US 11 62561828 62561828 single base substitution C T synonymous_variant T58T 174G>A UCEC-US 11 62561828 62561828 single base substitution C T synonymous_variant T597T 1791G>A UCEC-US 11 62561846 62561846 single base substitution G A 3_prime_UTR_variant UCEC-US 11 62561846 62561846 single base substitution G A downstream_gene_variant UCEC-US 11 62561846 62561846 single base substitution G A exon_variant UCEC-US 11 62561846 62561846 single base substitution G A synonymous_variant F52F 156C>T UCEC-US 11 62561846 62561846 single base substitution G A synonymous_variant F548F 1644C>T UCEC-US 11 62561846 62561846 single base substitution G A synonymous_variant F591F 1773C>T UCEC-US 11 62563574 62563574 single base substitution G A 3_prime_UTR_variant UCEC-US 11 62563574 62563574 single base substitution G A downstream_gene_variant UCEC-US 11 62563574 62563574 single base substitution G A exon_variant UCEC-US 11 62563574 62563574 single base substitution G A synonymous_variant D475D 1425C>T UCEC-US 11 62563574 62563574 single base substitution G A synonymous_variant D518D 1554C>T UCEC-US 11 62563574 62563574 single base substitution G A upstream_gene_variant UCEC-US 11 62563655 62563655 single base substitution T C downstream_gene_variant UCEC-US 11 62563655 62563655 single base substitution T C splice_acceptor_variant UCEC-US 11 62563655 62563655 single base substitution T C upstream_gene_variant UCEC-US 11 62568568 62568568 single base substitution C A downstream_gene_variant UCEC-US 11 62568568 62568568 single base substitution C A intron_variant UCEC-US 11 62568568 62568568 single base substitution C A stop_gained E165* 493G>T UCEC-US 11 62568568 62568568 single base substitution C A stop_gained E302* 904G>T UCEC-US 11 62568568 62568568 single base substitution C A stop_gained E345* 1033G>T UCEC-US 11 62568568 62568568 single base substitution C A upstream_gene_variant UCEC-US 11 62569083 62569083 single base substitution G A downstream_gene_variant UCEC-US 11 62569083 62569083 single base substitution G A intron_variant UCEC-US 11 62569083 62569083 single base substitution G A synonymous_variant Y220Y 660C>T UCEC-US 11 62569083 62569083 single base substitution G A synonymous_variant Y263Y 789C>T UCEC-US 11 62569083 62569083 single base substitution G A synonymous_variant Y83Y 249C>T UCEC-US 11 62569083 62569083 single base substitution G A upstream_gene_variant UCEC-US 11 62571027 62571027 single base substitution C A exon_variant UCEC-US 11 62571027 62571027 single base substitution C A intron_variant UCEC-US 11 62571027 62571027 single base substitution C A missense_variant R121L 362G>T UCEC-US 11 62571027 62571027 single base substitution C A missense_variant R18L 53G>T UCEC-US 11 62571027 62571027 single base substitution C A missense_variant R78L 233G>T UCEC-US 11 62571027 62571027 single base substitution C A upstream_gene_variant UCEC-US 11 62575006 62575006 single base substitution G A upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-66-2742-01 COSM689842 c.628G>A p.E210K Substitution - Missense 11:62801750-62801750 - TCGA-AC-A23H-01 COSM3809876 c.668C>G p.S223C Substitution - Missense 11:62801603-62801603 - PCSI_0083_Pa_X COSM3375889 c.1761-1G>T p.? Unknown 11:62792702-62792702 - 12T COSM109362 c.645C>T p.I215I Substitution - coding silent 11:62801626-62801626 - TCGA-27-1833-01 COSM3397996 c.1759A>G p.K587E Substitution - Missense 11:62794259-62794259 - 083-01-2TD COSM145702 c.635T>G p.L212R Substitution - Missense 11:62801743-62801743 - TCGA-AA-3956-01 COSM297133 c.1677G>A p.P559P Substitution - coding silent 11:62794341-62794341 - T3021 COSM4708835 c.709G>T p.D237Y Substitution - Missense 11:62801562-62801562 - T3225 COSM4708833 c.746G>A p.R249H Substitution - Missense 11:62801381-62801381 - YUKLAB COSM1704155 c.1004C>T p.S335F Substitution - Missense 11:62800389-62800389 - 083 COSM145702 c.635T>G p.L212R Substitution - Missense 11:62801743-62801743 - 35M COSM5581917 c.784G>A p.E262K Substitution - Missense 11:62801343-62801343 - T1154 COSM4708832 c.1627G>T p.E543* Substitution - Nonsense 11:62794391-62794391 - BD28T COSM5520063 c.1130A>G p.Y377C Substitution - Missense 11:62797231-62797231 - TCGA-AG-3882-01 COSM288447 c.142C>T p.R48W Substitution - Missense 11:62803865-62803865 - TCGA-ER-A19Q-06 COSM3451087 c.1024C>T p.R342C Substitution - Missense 11:62798568-62798568 - T2969 COSM4708841 c.58C>G p.Q20E Substitution - Missense 11:62803949-62803949 - TCGA-EK-A3GK-01 COSM4853611 c.34G>C p.D12H Substitution - Missense 11:62803973-62803973 - LIM1899 COSM4612986 c.1073_1074insC p.P359fs*5 Insertion - Frameshift 11:62797366-62797367 - 2492710 COSM5717586 c.334C>T p.Q112* Substitution - Nonsense 11:62803454-62803454 - CHC1915T COSM3667029 c.1674C>G p.S558R Substitution - Missense 11:62794344-62794344 - PD4120a COSM163041 c.10G>A p.E4K Substitution - Missense 11:62805347-62805347 - 2367115 COSM4997301 c.1814_1815insA p.H605fs*>16 Insertion - Frameshift 11:62792647-62792648 - TCGA-FP-A4BE-01 COSM1604923 c.1426G>A p.V476I Substitution - Missense 11:62796101-62796101 - 2521243 COSM5886735 c.93G>A p.W31* Substitution - Nonsense 11:62803914-62803914 - 8035823 COSM3383667 c.1744C>T p.L582F Substitution - Missense 11:62794274-62794274 - TCGA-AP-A0LM-01 COSM929826 c.1346-2A>G p.? Unknown 11:62796183-62796183 - TCGA-EK-A3GK-01 COSM4852693 c.250G>A p.D84N Substitution - Missense 11:62803538-62803538 - TCGA-FU-A3HY-01 COSM4838606 c.37G>C p.D13H Substitution - Missense 11:62803970-62803970 - HCT-116 COSM1684272 c.1097delC p.T368fs*16 Deletion - Frameshift 11:62797343-62797343 - CSCC-11-T COSM4469851 c.1622C>T p.S541F Substitution - Missense 11:62794396-62794396 - 023 COSM145700 c.64A>T p.K22* Substitution - Nonsense 11:62803943-62803943 - MDS-18 COSM211485 c.1314T>G p.D438E Substitution - Missense 11:62796318-62796318 - 18 COSM5015017 c.1017-2A>T p.? Unknown 11:62798577-62798577 - SC_9094 COSM429475 c.660C>T p.Y220Y Substitution - coding silent 11:62801611-62801611 - HT115 COSM2039739 c.520G>A p.A174T Substitution - Missense 11:62801980-62801980 - SC_9062 COSM1355469 c.1159G>A p.V387I Substitution - Missense 11:62797202-62797202 - TCGA-B0-5707-01 COSM467155 c.686T>C p.L229P Substitution - Missense 11:62801585-62801585 - TCGA-AO-A128-01 COSM3809872 c.986A>C p.D329A Substitution - Missense 11:62800407-62800407 - 2492709 COSM5717586 c.334C>T p.Q112* Substitution - Nonsense 11:62803454-62803454 - TCGA-G3-A25Y-01 COSM4917944 c.221C>A p.P74H Substitution - Missense 11:62803567-62803567 - TCGA-A2-A0T5-01 COSM3809882 c.11A>G p.E4G Substitution - Missense 11:62805346-62805346 - TCGA-EK-A3GK-01 COSM4853569 c.127G>A p.G43S Substitution - Missense 11:62803880-62803880 - TCGA-F1-6874-01 COSM4034904 c.487G>A p.V163I Substitution - Missense 11:62802013-62802013 - RK056_C01 COSM1628141 c.1607T>C p.V536A Substitution - Missense 11:62794411-62794411 - PCSI_0090_Pa_X COSM3375890 c.1122+4G>T p.? Unknown 11:62797314-62797314 - C086 COSM5535785 c.892C>T p.L298F Substitution - Missense 11:62801108-62801108 - T155 COSM1177260 c.1840G>T p.E614* Substitution - Nonsense 11:62792496-62792496 - TCGA-EP-A2KC-01 COSM4913762 c.1774A>T p.N592Y Substitution - Missense 11:62792688-62792688 - PD14459a COSM5773695 c.320G>A p.G107E Substitution - Missense 11:62803468-62803468 - 2292386 COSM4610629 c.1195G>A p.D399N Substitution - Missense 11:62796551-62796551 - ESCC_3 COSM5622542 c.204C>T p.P68P Substitution - coding silent 11:62803803-62803803 - TCGA-D7-A4YY-01 COSM4034898 c.942G>A p.G314G Substitution - coding silent 11:62800451-62800451 - SNU-175 COSM2039756 c.89G>A p.R30Q Substitution - Missense 11:62803918-62803918 - 023-0056-01TD COSM145700 c.64A>T p.K22* Substitution - Nonsense 11:62803943-62803943 - TCGA-AA-A00N-01 COSM276427 c.1180T>C p.Y394H Substitution - Missense 11:62796566-62796566 - ESCC_5 COSM5623099 c.1208G>A p.R403Q Substitution - Missense 11:62796538-62796538 - TCGA-BH-A0HF-01 COSM3809878 c.172G>A p.D58N Substitution - Missense 11:62803835-62803835 - TCGA-14-1037 COSM2155307 c.1456C>T p.Q486* Substitution - Nonsense 11:62796071-62796071 - RK143_C01 COSM3700113 c.1114C>T p.P372S Substitution - Missense 11:62797326-62797326 - TCGA-09-2051-01 COSM119982 c.226A>G p.T76A Substitution - Missense 11:62803562-62803562 - TCGA-A1-A0SI-01 COSM1475674 c.1152G>C p.K384N Substitution - Missense 11:62797209-62797209 - OSCC-GB_00990111 COSM4885704 c.1364T>C p.L455P Substitution - Missense 11:62796163-62796163 - STC246 COSM5050970 c.525C>A p.V175V Substitution - coding silent 11:62801975-62801975 - PD9696a COSM5782609 c.454-7C>G p.? Unknown 11:62802053-62802053 - TCGA-66-2787-01 COSM689843 c.873C>A p.P291P Substitution - coding silent 11:62801127-62801127 - TCGA-EA-A3QD-01 COSM4821851 c.945G>A p.L315L Substitution - coding silent 11:62800448-62800448 - TCGA-66-2754-01 COSM689844 c.896C>G p.S299C Substitution - Missense 11:62801104-62801104 - C608 COSM4442690 c.1286G>A p.R429Q Substitution - Missense 11:62796460-62796460 - TCGA-BR-7707-01 COSM3451091 c.590C>T p.P197L Substitution - Missense 11:62801788-62801788 - TCGA-D8-A1JA-01 COSM3809874 c.960C>G p.L320L Substitution - coding silent 11:62800433-62800433 - PCSI_0090_Pa_X COSM3375891 c.639+2T>C p.? Unknown 11:62801737-62801737 - TCGA-AP-A051-01 COSM929824 c.1662G>A p.T554T Substitution - coding silent 11:62794356-62794356 - T2940 COSM4708831 c.1698G>A p.E566E Substitution - coding silent 11:62794320-62794320 - CHC1915T COSM3667029 c.1674C>G p.S558R Substitution - Missense 11:62794344-62794344 - TCGA-DK-A2I4-01 COSM3791723 c.351G>A p.K117K Substitution - coding silent 11:62803437-62803437 - CSCC-35-T COSM109131 c.373C>T p.P125S Substitution - Missense 11:62802257-62802257 - MZ7-mel COSM22117 c.1161C>T p.V387V Substitution - coding silent 11:62797200-62797200 - YUMER COSM1704157 c.152G>A p.R51H Substitution - Missense 11:62803855-62803855 - 8068988 COSM4388231 c.1505-6T>C p.? Unknown 11:62795013-62795013 - TCGA-BR-7851-01 COSM4034906 c.413T>C p.M138T Substitution - Missense 11:62802217-62802217 - I2L-P14b-Tumor-Organoid COSM5360529 c.205C>T p.R69* Substitution - Nonsense 11:62803802-62803802 - TCGA-A5-A0VP-01 COSM929825 c.1425C>T p.D475D Substitution - coding silent 11:62796102-62796102 - HN_62814 COSM124896 c.1319G>A p.R440K Substitution - Missense 11:62796313-62796313 - 12T COSM109131 c.373C>T p.P125S Substitution - Missense 11:62802257-62802257 - HCC110 COSM1604923 c.1426G>A p.V476I Substitution - Missense 11:62796101-62796101 - TCGA-DD-A1EH-01 COSM4934177 c.1024C>G p.R342G Substitution - Missense 11:62798568-62798568 - RK308_C01 COSM3739192 c.1171C>A p.L391M Substitution - Missense 11:62797190-62797190 - TCGA-BS-A0TJ-01 COSM929829 c.43C>T p.R15C Substitution - Missense 11:62803964-62803964 - TCGA-DK-A1AC-01 COSM1298339 c.1278C>G p.N426K Substitution - Missense 11:62796468-62796468 - cSCCP6 COSM136845 c.1054G>A p.D352N Substitution - Missense 11:62797386-62797386 - YUTUCO COSM3451093 c.486C>T p.F162F Substitution - coding silent 11:62802014-62802014 - TCGA-AP-A051-01 COSM429475 c.660C>T p.Y220Y Substitution - coding silent 11:62801611-62801611 - SW620 COSM2039760 c.37G>A p.D13N Substitution - Missense 11:62803970-62803970 - TCGA-R2-A69V-01 COSM4851082 c.994C>A p.R332R Substitution - coding silent 11:62800399-62800399 - RD COSM1197207 c.1407G>T p.L469F Substitution - Missense 11:62796120-62796120 - PD5141a COSM3719644 c.1228T>A p.Y410N Substitution - Missense 11:62796518-62796518 - TCGA-EB-A430-01 COSM3451088 c.792C>T p.I264I Substitution - coding silent 11:62801335-62801335 - PCSI_0083_Pa_P_526 COSM3375889 c.1761-1G>T p.? Unknown 11:62792702-62792702 - SCC-25 COSM4597351 c.640C>G p.L214V Substitution - Missense 11:62801631-62801631 - TCGA-B0-4816-01 COSM467156 c.664G>C p.G222R Substitution - Missense 11:62801607-62801607 - T28 COSM5619173 c.1209A>G p.R403R Substitution - coding silent 11:62796537-62796537 - TCGA-EK-A3GK-01 COSM4852635 c.143G>A p.R48Q Substitution - Missense 11:62803864-62803864 - TCGA-D1-A101-01 COSM929828 c.233G>T p.R78L Substitution - Missense 11:62803555-62803555 - T3021 COSM4708839 c.339T>C p.D113D Substitution - coding silent 11:62803449-62803449 - S02243 COSM5677635 c.383G>C p.R128T Substitution - Missense 11:62802247-62802247 - TCGA-BS-A0UV-01 COSM929822 c.1811C>T p.T604I Substitution - Missense 11:62792651-62792651 - TCGA-AA-A02J-01 COSM300790 c.1644C>T p.F548F Substitution - coding silent 11:62794374-62794374 - TCGA-EB-A41A-01 COSM109362 c.645C>T p.I215I Substitution - coding silent 11:62801626-62801626 - PCSI_0083_Pa_P COSM3375889 c.1761-1G>T p.? Unknown 11:62792702-62792702 - TCGA-D1-A17Q-01 COSM929827 c.904G>T p.E302* Substitution - Nonsense 11:62801096-62801096 - LIM1215 COSM4639340 c.1520G>A p.R507Q Substitution - Missense 11:62794992-62794992 - LXFL529 COSM1197207 c.1407G>T p.L469F Substitution - Missense 11:62796120-62796120 - TCGA-ER-A19M-06 COSM3451086 c.1141G>A p.E381K Substitution - Missense 11:62797220-62797220 - 8069453 COSM3769385 c.995G>A p.R332Q Substitution - Missense 11:62800398-62800398 - 40M COSM5585997 c.993C>T p.F331F Substitution - coding silent 11:62800400-62800400 - TCGA-CA-6718-01 COSM1355470 c.839T>G p.L280R Substitution - Missense 11:62801161-62801161 - 587376 COSM1218131 c.1191T>G p.I397M Substitution - Missense 11:62796555-62796555 - tumor_4177376 COSM2039738 c.553C>T p.R185* Substitution - Nonsense 11:62801947-62801947 - CSCC-29-T COSM4450360 c.559-1G>A p.? Unknown 11:62801820-62801820 - pfg122T COSM4756390 c.1070C>T p.P357L Substitution - Missense 11:62797370-62797370 - 64 COSM5015016 c.1030C>T p.R344* Substitution - Nonsense 11:62798562-62798562 - 056-01-1TD COSM145700 c.64A>T p.K22* Substitution - Nonsense 11:62803943-62803943 - DLD1 COSM4622228 c.151C>T p.R51C Substitution - Missense 11:62803856-62803856 - TCGA-GI-A2C8-01 COSM1475673 c.1719A>G p.A573A Substitution - coding silent 11:62794299-62794299 - T55 COSM4708837 c.639+1G>A p.? Unknown 11:62801738-62801738 - TCGA-BR-8680-01 COSM4034897 c.1141G>T p.E381* Substitution - Nonsense 11:62797220-62797220 - TCGA-AG-A002-01 COSM262491 c.1031G>A p.R344Q Substitution - Missense 11:62798561-62798561 - TCGA-AP-A056-01 COSM300790 c.1644C>T p.F548F Substitution - coding silent 11:62794374-62794374 - TCGA-AA-A022-01 COSM300487 c.1481_1482delCT p.S494fs*29 Deletion - Frameshift 11:62795923-62795924 - TCGA-D3-A5GS-06 COSM3451085 c.1571A>T p.N524I Substitution - Missense 11:62794941-62794941 - 2492708 COSM5717586 c.334C>T p.Q112* Substitution - Nonsense 11:62803454-62803454 - CSCC-55-T COSM4499555 c.544C>T p.R182W Substitution - Missense 11:62801956-62801956 - I2L-P14b-Tumor-Biopsy COSM5360529 c.205C>T p.R69* Substitution - Nonsense 11:62803802-62803802 - TCGA-A5-A0G9-01 COSM929823 c.1746C>T p.L582L Substitution - coding silent 11:62794272-62794272 - HCT116 COSM2039725 c.1101delC p.T368fs*16 Deletion - Frameshift 11:62797339-62797339 - TCGA-BT-A20J-01 COSM415484 c.648G>C p.M216I Substitution - Missense 11:62801623-62801623 - TCGA-DK-A3WW-01 COSM3791720 c.1266C>T p.F422F Substitution - coding silent 11:62796480-62796480 - TCGA-G2-A3VY-01 COSM3791719 c.1606G>C p.V536L Substitution - Missense 11:62794412-62794412 - TCGA-A3-3363-01 COSM1492619 c.657A>T p.R219R Substitution - coding silent 11:62801614-62801614 - 082-02-1TD COSM145701 c.232C>T p.R78* Substitution - Nonsense 11:62803556-62803556 - TCGA-FS-A4F5-06 COSM3451091 c.590C>T p.P197L Substitution - Missense 11:62801788-62801788 - TCGA-AA-3663-01 COSM1355467 c.1299C>A p.A433A Substitution - coding silent 11:62796333-62796333 - SNU-175 COSM2039741 c.507C>A p.A169A Substitution - coding silent 11:62801993-62801993 - SNU-C2B COSM2039755 c.112C>T p.R38C Substitution - Missense 11:62803895-62803895 - TCGA-DA-A1I4-06 COSM3451093 c.486C>T p.F162F Substitution - coding silent 11:62802014-62802014 - 082 COSM145701 c.232C>T p.R78* Substitution - Nonsense 11:62803556-62803556 - pfg122T COSM4756389 c.1463G>T p.S488I Substitution - Missense 11:62795942-62795942 - TCGA-F1-A448-01 COSM4034900 c.697C>T p.R233C Substitution - Missense 11:62801574-62801574 - PCSI_0009_Pa_X COSM3375893 c.101G>C p.G34A Substitution - Missense 11:62803906-62803906 - I2L-P19Tb-Tumor-Organoid COSM5360708 c.1025G>A p.R342H Substitution - Missense 11:62798567-62798567 - YUWAND COSM1704156 c.745C>T p.R249C Substitution - Missense 11:62801382-62801382 - XHDG03 COSM4767934 c.773G>A p.R258K Substitution - Missense 11:62801354-62801354 - TCGA-A8-A0A6-01 COSM3809880 c.91T>G p.W31G Substitution - Missense 11:62803916-62803916 - TCGA-EI-6917-01 COSM3416075 c.370-1G>A p.? Unknown 11:62802261-62802261 - I2L-P19Tb-Tumor-Biopsy COSM5360708 c.1025G>A p.R342H Substitution - Missense 11:62798567-62798567 - TCGA-A8-A08P-01 COSM429473 c.1571A>G p.N524S Substitution - Missense 11:62794941-62794941 - RMS008 COSM5880390 c.1532G>A p.R511Q Substitution - Missense 11:62794980-62794980 - TCGA-DK-A2I4-01 COSM3791721 c.483C>G p.F161L Substitution - Missense 11:62802017-62802017 - ZZUFHECRKL-G034T COSM5440238 c.1383C>T p.N461N Substitution - coding silent 11:62796144-62796144 - TCGA-BR-6452-01 COSM4034902 c.667T>C p.S223P Substitution - Missense 11:62801604-62801604 - HCC110T COSM1604923 c.1426G>A p.V476I Substitution - Missense 11:62796101-62796101 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.523739 11q12-q13 602647 2401692|CGAP|BC004904|A/G|coding|Arg403Arg|1281|Validated; 2401692|CGAP|BC028041|A/G|coding|Arg403Arg|1274|Validated; 2401693|CGAP|BC028041|C/G|non-coding||2240|Candidate; 2401694|CGAP|BC004904|A/C|non-coding||2149|Candidate; 2401694|CGAP|BC028041|A/C|non-coding||2142|Candidate

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.L212R c.635T>G 11 62569215 CLL A G Missense p.V536A c.1607T>C 11 62561883 HC C A Missense p.R26L c.77G>T 11 62571402 CM C A Missense p.R78L c.233G>T 11 62571027 UCEC C A Nonsense p.E183* c.547G>T 11 62569425 LUAD C A SpliceAcceptorSNV . c.799-1G>T 11 62568674 LUAD CC TT Missense p.R507Q c.1520_1521delinsAA 11 62562463 CM C G Missense p.G222R c.664G>C 11 62569079 RCCC C G Missense p.K384N c.1152G>C 11 62564681 BRCA C G Missense p.M216I c.648G>C 11 62569095 BLCA C T 3-UTRSNV . c.1857+112G>A 11 62559839 CM C T Missense p.D221N c.661G>A 11 62569082 HNSC C T Missense p.E210K c.628G>A 11 62569222 LUSC C T Missense p.E4K c.10G>A 11 62572819 BRCA C T Missense p.R440K c.1319G>A 11 62563785 HNSC C T Missense p.V163I c.487G>A 11 62569485 STAD C T Synonymous p.K117K c.351G>A 11 62570909 BLCA C T Synonymous p.P559P c.1677G>A 11 62561813 COREAD G A 3-UTRSNV . c.1857+135C>T 11 62559816 CM G A 5-UTRSNV . c.1-24C>T 11 62572852 CM G A 5-UTRSNV . c.1-30C>T 11 62572858 BRCA G A IntronicSNV . c.1016+21C>T 11 62567828 CM G A IntronicSNV . c.1016+44C>T 11 62567805 CM G A IntronicSNV . c.1017-86C>T 11 62566133 CM G A Missense p.A64V c.191C>T 11 62571288 LUAD G A Missense p.P28L c.83C>T 11 62571396 HNSC G A Missense p.P371L c.1112C>T 11 62564800 BRCA G A Missense p.R342C c.1024C>T 11 62566040 CM G A Missense p.R48W c.142C>T 11 62571337 COREAD G A Missense p.T369M c.1106C>T 11 62564806 HNSC G A Synonymous p.D475D c.1425C>T 11 62563574 UCEC G A Synonymous p.F162F c.486C>T 11 62569486 CM G A Synonymous p.F548F c.1644C>T 11 62561846 COREAD G A Synonymous p.L204L c.610C>T 11 62569240 CM G A Synonymous p.L582L c.1746C>T 11 62561744 UCEC G A Synonymous p.N192N c.576C>T 11 62569274 LUAD G A Synonymous p.Y220Y c.660C>T 11 62569083 BRCA G A Synonymous p.Y72Y c.216C>T 11 62571044 CM G C Missense p.F161L c.483C>G 11 62569489 BLCA G C Missense p.S299C c.896C>G 11 62568576 LUSC GG AT SpliceDonorBlockSubstitution . c.1284_1285delinsAT 11 62563933 CM G T Missense p.P236Q c.707C>A 11 62569036 LUAD G T Synonymous p.P291P c.873C>A 11 62568599 LUSC GTT - InFrameDeletion p.N593delN c.1777_1779delAAC 11 62560155 BLCA T A Nonsense p.K22* c.64A>T 11 62571415 CLL T C 5-UTRSNV . c.1-62A>G 11 62572890 BRCA T C Missense p.K587E c.1759A>G 11 62561731 GBM T C Missense p.N524S c.1571A>G 11 62562413 BRCA T C Missense p.T76A c.226A>G 11 62571034 OV T C Synonymous p.A573A c.1719A>G 11 62561771 BRCA