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 6 28872409 28872409 + Missense_Mutation SNP G G C TCGA-OR-A5KB-01A-11D-A30A-10 TCGA-OR-A5KB-11A-11D-A30A-10 g.chr6:28872409G>C c.980C>G c.(979-981)cCc>cGc p.P327R BLCA 6 28872256 28872256 + Missense_Mutation SNP C C T TCGA-FD-A3SS-01A-12D-A22Z-08 TCGA-FD-A3SS-10A-01D-A22Z-08 g.chr6:28872256C>T c.1133G>A c.(1132-1134)gGa>gAa p.G378E BLCA 6 28872291 28872291 + Silent SNP G G A TCGA-DK-A6B6-01A-11D-A30E-08 TCGA-DK-A6B6-10A-01D-A30H-08 g.chr6:28872291G>A c.1098C>T c.(1096-1098)ttC>ttT p.F366F BLCA 6 28875040 28875040 + Splice_Site SNP C C T TCGA-K4-A5RJ-01A-11D-A289-08 TCGA-K4-A5RJ-10A-01D-A289-08 g.chr6:28875040C>T c.e7-1 BLCA 6 28876613 28876613 + Missense_Mutation SNP T T G TCGA-DK-A6AW-01A-11D-A30E-08 TCGA-DK-A6AW-10A-01D-A30H-08 g.chr6:28876613T>G c.891A>C c.(889-891)aaA>aaC p.K297N BLCA 6 28879489 28879489 + Missense_Mutation SNP C C T TCGA-XF-AAN2-01A-11D-A42E-08 TCGA-XF-AAN2-10A-01D-A42H-08 g.chr6:28879489C>T c.754G>A c.(754-756)Ggg>Agg p.G252R BLCA 6 28889686 28889686 + Missense_Mutation SNP C C T TCGA-DK-A1AD-01A-11D-A13W-08 TCGA-DK-A1AD-10A-01D-A13W-08 g.chr6:28889686C>T c.499G>A c.(499-501)Gca>Aca p.A167T BLCA 6 28889711 28889711 + Silent SNP C C T TCGA-XF-A9SJ-01A-11D-A391-08 TCGA-XF-A9SJ-10A-01D-A394-08 g.chr6:28889711C>T c.474G>A c.(472-474)aaG>aaA p.K158K BLCA 6 28891284 28891284 + Silent SNP G G A TCGA-DK-A1A6-01A-11D-A13W-08 TCGA-DK-A1A6-10A-01D-A13W-08 g.chr6:28891284G>A c.126C>T c.(124-126)cgC>cgT p.R42R BRCA 6 28872023 28872023 + Missense_Mutation SNP A A C TCGA-A8-A0A6-01A-12W-A071-09 TCGA-A8-A0A6-10A-01W-A071-09 g.chr6:28872023A>C c.1366T>G c.(1366-1368)Tgt>Ggt p.C456G BRCA 6 28876593 28876593 + Missense_Mutation SNP T T C TCGA-BH-A18G-01A-11D-A12B-09 TCGA-BH-A18G-10A-01D-A12B-09 g.chr6:28876593T>C c.911A>G c.(910-912)aAa>aGa p.K304R COAD 6 28872120 28872120 + Silent SNP T T C TCGA-AA-A00A-01A-01W-A005-10 TCGA-AA-A00A-10A-01W-A005-10 g.chr6:28872120T>C c.1269A>G c.(1267-1269)ccA>ccG p.P423P COAD 6 28891383 28891383 + Silent SNP G G A TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr6:28891383G>A c.27C>T c.(25-27)tgC>tgT p.C9C COADREAD 6 28872120 28872120 + Silent SNP T T C TCGA-AA-A00A-01A-01W-A005-10 TCGA-AA-A00A-10A-01W-A005-10 g.chr6:28872120T>C c.1269A>G c.(1267-1269)ccA>ccG p.P423P COADREAD 6 28876838 28876838 + Silent SNP A A T TCGA-AG-3609-01A-02W-0833-10 TCGA-AG-3609-10A-01W-0833-10 g.chr6:28876838A>T c.798T>A c.(796-798)ccT>ccA p.P266P COADREAD 6 28891383 28891383 + Silent SNP G G A TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr6:28891383G>A c.27C>T c.(25-27)tgC>tgT p.C9C ESCA 6 28875015 28875015 + Missense_Mutation SNP G G A TCGA-IG-A3YC-01A-11D-A247-09 TCGA-IG-A3YC-10A-01D-A247-09 g.chr6:28875015G>A c.944C>T c.(943-945)tCa>tTa p.S315L ESCA 6 28876806 28876806 + Missense_Mutation SNP A A C TCGA-VR-A8EY-01A-11D-A36J-09 TCGA-VR-A8EY-10A-01D-A36M-09 g.chr6:28876806A>C c.830T>G c.(829-831)aTc>aGc p.I277S ESCA 6 28876863 28876863 + Missense_Mutation SNP G G T TCGA-VR-A8EX-01A-11D-A36J-09 TCGA-VR-A8EX-10A-01D-A36M-09 g.chr6:28876863G>T c.773C>A c.(772-774)gCt>gAt p.A258D ESCA 6 28889703 28889703 + Missense_Mutation SNP C C T TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr6:28889703C>T c.482G>A c.(481-483)cGg>cAg p.R161Q ESCA 6 28891220 28891220 + Missense_Mutation SNP G G A TCGA-R6-A6L4-01A-11D-A31U-09 TCGA-R6-A6L4-10A-01D-A31U-09 g.chr6:28891220G>A c.190C>T c.(190-192)Cac>Tac p.H64Y GBMLGG 6 28872363 28872363 + Nonsense_Mutation SNP G G T TCGA-DU-A6S3-01A-12D-A32B-08 TCGA-DU-A6S3-10A-01D-A329-08 g.chr6:28872363G>T c.1026C>A c.(1024-1026)taC>taA p.Y342* GBMLGG 6 28887928 28887928 + Missense_Mutation SNP C C T TCGA-P5-A781-01A-11D-A32B-08 TCGA-P5-A781-10A-01D-A329-08 g.chr6:28887928C>T c.608G>A c.(607-609)cGc>cAc p.R203H HNSC 6 28871857 28871857 + Missense_Mutation SNP G G C TCGA-IQ-7632-01A-11D-2078-08 TCGA-IQ-7632-10A-01D-2078-08 g.chr6:28871857G>C c.1532C>G c.(1531-1533)aCc>aGc p.T511S HNSC 6 28871930 28871930 + Missense_Mutation SNP G G C TCGA-CV-6948-01A-11D-1912-08 TCGA-CV-6948-10A-01D-1912-08 g.chr6:28871930G>C c.1459C>G c.(1459-1461)Ctg>Gtg p.L487V HNSC 6 28871933 28871933 + Missense_Mutation SNP G G A TCGA-CQ-7068-01A-11D-2078-08 TCGA-CQ-7068-10A-01D-2078-08 g.chr6:28871933G>A c.1456C>T c.(1456-1458)Cct>Tct p.P486S HNSC 6 28872268 28872268 + Missense_Mutation SNP T T A TCGA-UF-A7JK-01A-11D-A34J-08 TCGA-UF-A7JK-10A-01D-A34M-08 g.chr6:28872268T>A c.1121A>T c.(1120-1122)gAg>gTg p.E374V HNSC 6 28872323 28872323 + Missense_Mutation SNP G G T TCGA-CN-A6V1-01A-12D-A34J-08 TCGA-CN-A6V1-10B-01D-A34M-08 g.chr6:28872323G>T c.1066C>A c.(1066-1068)Ctg>Atg p.L356M HNSC 6 28872383 28872383 + Missense_Mutation SNP G G A TCGA-BA-5149-01A-01D-1512-08 TCGA-BA-5149-10A-01D-1512-08 g.chr6:28872383G>A c.1006C>T c.(1006-1008)Cgg>Tgg p.R336W HNSC 6 28876602 28876602 + Missense_Mutation SNP T T A TCGA-BA-4078-01A-01D-1434-08 TCGA-BA-4078-10A-01D-1434-08 g.chr6:28876602T>A c.902A>T c.(901-903)gAt>gTt p.D301V HNSC 6 28887838 28887838 + Missense_Mutation SNP A A T TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr6:28887838A>T c.698T>A c.(697-699)aTc>aAc p.I233N LGG 6 28872363 28872363 + Nonsense_Mutation SNP G G T TCGA-DU-A6S3-01A-12D-A32B-08 TCGA-DU-A6S3-10A-01D-A329-08 g.chr6:28872363G>T c.1026C>A c.(1024-1026)taC>taA p.Y342* LGG 6 28887928 28887928 + Missense_Mutation SNP C C T TCGA-P5-A781-01A-11D-A32B-08 TCGA-P5-A781-10A-01D-A329-08 g.chr6:28887928C>T c.608G>A c.(607-609)cGc>cAc p.R203H LIHC 6 28876789 28876789 + Nonsense_Mutation SNP T T A TCGA-CC-A7IK-01A-12D-A33Q-10 TCGA-CC-A7IK-10A-01D-A33Q-10 g.chr6:28876789T>A c.847A>T c.(847-849)Aaa>Taa p.K283* LIHC 6 28887983 28887983 + Frame_Shift_Del DEL C C - TCGA-G3-A3CJ-01A-11D-A20W-10 TCGA-G3-A3CJ-10A-01D-A20W-10 g.chr6:28887983delC c.553delG c.(553-555)gagfs p.E185fs LUAD 6 28872087 28872087 + Missense_Mutation SNP C C A TCGA-55-7914-01A-11D-2167-08 TCGA-55-7914-10A-01D-2167-08 g.chr6:28872087C>A c.1302G>T c.(1300-1302)caG>caT p.Q434H LUAD 6 28872184 28872184 + Missense_Mutation SNP G G C TCGA-05-4424-01A-22D-1855-08 TCGA-05-4424-10A-01D-1855-08 g.chr6:28872184G>C c.1205C>G c.(1204-1206)cCc>cGc p.P402R LUAD 6 28872209 28872209 + Silent SNP T T G TCGA-78-8662-01A-11D-2393-08 TCGA-78-8662-10A-01D-2393-08 g.chr6:28872209T>G c.1180A>C c.(1180-1182)Aga>Cga p.R394R LUAD 6 28872311 28872311 + Missense_Mutation SNP C C A TCGA-49-4494-01A-01D-1265-08 TCGA-49-4494-11A-01D-1265-08 g.chr6:28872311C>A c.1078G>T c.(1078-1080)Gtc>Ttc p.V360F LUAD 6 28872321 28872321 + Silent SNP C C A TCGA-44-5644-01A-21D-2036-08 TCGA-44-5644-10A-01D-2036-08 g.chr6:28872321C>A c.1068G>T c.(1066-1068)ctG>ctT p.L356L LUAD 6 28872429 28872429 + Silent SNP C C G TCGA-97-7554-01A-11D-2036-08 TCGA-97-7554-10A-01D-2036-08 g.chr6:28872429C>G c.960G>C c.(958-960)ctG>ctC p.L320L LUAD 6 28876835 28876835 + Missense_Mutation SNP C C A TCGA-05-4398-01A-01D-1265-08 TCGA-05-4398-10A-01D-1265-08 g.chr6:28876835C>A c.801G>T c.(799-801)tgG>tgT p.W267C LUAD 6 28887798 28887798 + Missense_Mutation SNP C C A TCGA-97-7938-01A-11D-2167-08 TCGA-97-7938-10A-01D-2167-08 g.chr6:28887798C>A c.738G>T c.(736-738)gaG>gaT p.E246D LUAD 6 28891242 28891242 + Missense_Mutation SNP G G C TCGA-78-7149-01A-11D-2036-08 TCGA-78-7149-10A-01D-2036-08 g.chr6:28891242G>C c.168C>G c.(166-168)tgC>tgG p.C56W OV 6 28872365 28872365 + Frame_Shift_Del DEL A A - TCGA-24-2290-01A-01W-0799-08 TCGA-24-2290-10A-01W-0799-08 g.chr6:28872365delA c.1024delT c.(1024-1026)tacfs p.Y342fs PRAD 6 28891196 28891196 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr6:28891196C>T c.214G>A c.(214-216)Gcc>Acc p.A72T READ 6 28876838 28876838 + Silent SNP A A T TCGA-AG-3609-01A-02W-0833-10 TCGA-AG-3609-10A-01W-0833-10 g.chr6:28876838A>T c.798T>A c.(796-798)ccT>ccA p.P266P SARC 6 28872289 28872289 + Missense_Mutation SNP A A T TCGA-DX-AB2E-01A-11D-A38Z-09 TCGA-DX-AB2E-10A-01D-A38Z-09 g.chr6:28872289A>T c.1100T>A c.(1099-1101)aTc>aAc p.I367N SARC 6 28872290 28872290 + Missense_Mutation SNP T T C TCGA-DX-AB2E-01A-11D-A38Z-09 TCGA-DX-AB2E-10A-01D-A38Z-09 g.chr6:28872290T>C c.1099A>G c.(1099-1101)Atc>Gtc p.I367V SARC 6 28888004 28888004 + Missense_Mutation SNP C C T TCGA-X9-A973-01A-11D-A387-09 TCGA-X9-A973-10A-01D-A38A-09 g.chr6:28888004C>T c.532G>A c.(532-534)Gag>Aag p.E178K SKCM 6 28872083 28872083 + Missense_Mutation SNP C C A TCGA-D9-A149-06A-11D-A196-08 TCGA-D9-A149-10A-01D-A198-08 g.chr6:28872083C>A c.1306G>T c.(1306-1308)Gtg>Ttg p.V436L SKCM 6 28872105 28872105 + Silent SNP G G A TCGA-EE-A3J5-06A-11D-A20D-08 TCGA-EE-A3J5-10A-01D-A20D-08 g.chr6:28872105G>A c.1284C>T c.(1282-1284)ccC>ccT p.P428P SKCM 6 28872284 28872284 + Missense_Mutation SNP C C A TCGA-EE-A2GT-06A-12D-A197-08 TCGA-EE-A2GT-10A-01D-A199-08 g.chr6:28872284C>A c.1105G>T c.(1105-1107)Ggg>Tgg p.G369W SKCM 6 28872399 28872399 + Silent SNP G G A TCGA-FS-A1ZK-06A-11D-A197-08 TCGA-FS-A1ZK-10A-01D-A199-08 g.chr6:28872399G>A c.990C>T c.(988-990)atC>atT p.I330I SKCM 6 28876588 28876588 + Nonsense_Mutation SNP G G A TCGA-FS-A1ZP-06A-11D-A197-08 TCGA-FS-A1ZP-10A-01D-A199-08 g.chr6:28876588G>A c.916C>T c.(916-918)Caa>Taa p.Q306* SKCM 6 28887960 28887960 + Silent SNP G G A TCGA-EE-A2A2-06A-11D-A196-08 TCGA-EE-A2A2-10A-01D-A198-08 g.chr6:28887960G>A c.576C>T c.(574-576)tcC>tcT p.S192S SKCM 6 28887961 28887961 + Missense_Mutation SNP G G A TCGA-EE-A2A2-06A-11D-A196-08 TCGA-EE-A2A2-10A-01D-A198-08 g.chr6:28887961G>A c.575C>T c.(574-576)tCc>tTc p.S192F SKCM 6 28888011 28888011 + Silent SNP G G A TCGA-ER-A193-06A-12D-A197-08 TCGA-ER-A193-10A-01D-A199-08 g.chr6:28888011G>A c.525C>T c.(523-525)acC>acT p.T175T SKCM 6 28889744 28889744 + Frame_Shift_Del DEL G G - TCGA-EE-A3JI-06A-11D-A21A-08 TCGA-EE-A3JI-10A-01D-A21A-08 g.chr6:28889744delG c.441delC c.(439-441)ctcfs p.L147fs

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand S01366 COSM316135 c.901G>C p.D301H Substitution - Missense 6:28908826-28908826 - S01366 COSM316135 c.901G>C p.D301H Substitution - Missense 6:28908826-28908826 - LUAD-F00282 COSM367417 c.1481G>T p.G494V Substitution - Missense 6:28904131-28904131 - 8058184 COSM3394038 c.748-3C>T p.? Unknown 6:28911721-28911721 - KPOPBR-60-T COSM5496136 c.1172C>T p.S391L Substitution - Missense 6:28904440-28904440 - 7285 COSM5615649 c.1421T>G p.F474C Substitution - Missense 6:28904191-28904191 - tumor_4144951 COSM5948855 c.748-9C>T p.? Unknown 6:28911727-28911727 - TCGA-FS-A1ZK-06 COSM3623861 c.990C>T p.I330I Substitution - coding silent 6:28904622-28904622 - HCA7 COSM3250152 c.1518T>C p.G506G Substitution - coding silent 6:28904094-28904094 - DLD1 COSM4625739 c.316T>C p.Y106H Substitution - Missense 6:28923317-28923317 - S02342 COSM5692981 c.892A>T p.M298L Substitution - Missense 6:28908835-28908835 - TCGA-DK-A1AD-01 COSM1311924 c.499G>A p.A167T Substitution - Missense 6:28921909-28921909 - BD246T COSM5496136 c.1172C>T p.S391L Substitution - Missense 6:28904440-28904440 - PT28 COSM5906334 c.1283C>T p.P428L Substitution - Missense 6:28904329-28904329 - TCGA-BR-8690-01 COSM3861209 c.1290G>A p.R430R Substitution - coding silent 6:28904322-28904322 - TCGA-D9-A149-06 COSM3623857 c.1306G>T p.V436L Substitution - Missense 6:28904306-28904306 - TCGA-EB-A430-01 COSM3623858 c.1300C>T p.Q434* Substitution - Nonsense 6:28904312-28904312 - pfg068T COSM4746857 c.1346_1348delTCT p.F449delF Deletion - In frame 6:28904264-28904266 - 230 COSM3730425 c.770+2T>C p.? Unknown 6:28911694-28911694 - TCGA-EE-A3J5-06 COSM3623859 c.1284C>T p.P428P Substitution - coding silent 6:28904328-28904328 - PT21_2 COSM5901465 c.1091C>T p.P364L Substitution - Missense 6:28904521-28904521 - PT36 COSM5915621 c.844C>T p.Q282* Substitution - Nonsense 6:28909015-28909015 - 2293782 COSM4609225 c.506C>A p.A169D Substitution - Missense 6:28921902-28921902 - PD24182a COSM5790900 c.325G>A p.E109K Substitution - Missense 6:28923308-28923308 - TCGA-DK-A1A6-01 COSM1311925 c.126C>T p.R42R Substitution - coding silent 6:28923507-28923507 - TCGA-EE-A2GT-06 COSM3623860 c.1105G>T p.G369W Substitution - Missense 6:28904507-28904507 - 61 COSM5737516 c.1279C>A p.L427I Substitution - Missense 6:28904333-28904333 - BN26 COSM1621345 c.862A>G p.T288A Substitution - Missense 6:28908997-28908997 - AOCS-124-1-X COSM4153191 c.180C>T p.F60F Substitution - coding silent 6:28923453-28923453 - sysucc-1116T COSM5483108 c.971C>T p.T324M Substitution - Missense 6:28904641-28904641 - CSCC-7-T COSM4463515 c.1295C>T p.P432L Substitution - Missense 6:28904317-28904317 - TCGA-AG-3609-01 COSM288144 c.798T>A p.P266P Substitution - coding silent 6:28909061-28909061 - TCGA-AA-3697-01 COSM3761759 c.234A>G p.V78V Substitution - coding silent 6:28923399-28923399 - HCT15 COSM4625740 c.60G>A p.L20L Substitution - coding silent 6:28923573-28923573 - KPOPBR-60-T COSM5963725 c.1199C>A p.S400* Substitution - Nonsense 6:28904413-28904413 - TCGA-A5-A0G9-01 COSM1077174 c.1505T>C p.V502A Substitution - Missense 6:28904107-28904107 - TCGA-FS-A1ZP-06 COSM3623862 c.916C>T p.Q306* Substitution - Nonsense 6:28908811-28908811 - CN-AML-CR-4-Dx COSM5427003 c.247A>C p.T83P Substitution - Missense 6:28923386-28923386 - TCGA-A8-A0A6-01 COSM3829914 c.1366T>G p.C456G Substitution - Missense 6:28904246-28904246 - ccRCC-35 COSM1664679 c.1128G>T p.E376D Substitution - Missense 6:28904484-28904484 - TCGA-F1-6177-01 COSM3861208 c.1304G>A p.R435Q Substitution - Missense 6:28904308-28904308 - TCGA-ER-A193-06 COSM3623863 c.525C>T p.T175T Substitution - coding silent 6:28920234-28920234 - BN26T COSM1621345 c.862A>G p.T288A Substitution - Missense 6:28908997-28908997 - DLD1 COSM4625740 c.60G>A p.L20L Substitution - coding silent 6:28923573-28923573 - 11-P8004 COSM4586541 c.702T>C p.A234A Substitution - coding silent 6:28920057-28920057 - ESO-805 COSM1268523 c.318C>A p.Y106* Substitution - Nonsense 6:28923315-28923315 - TCGA-AP-A056-01 COSM1077176 c.503G>A p.R168Q Substitution - Missense 6:28921905-28921905 - TCGA-B7-5816-01 COSM3250171 c.863C>T p.T288M Substitution - Missense 6:28908996-28908996 - HCT15 COSM4625739 c.316T>C p.Y106H Substitution - Missense 6:28923317-28923317 - TCGA-F5-6814-01 COSM3430422 c.134G>A p.G45D Substitution - Missense 6:28923499-28923499 - HCC5T COSM3662334 c.1490G>T p.G497V Substitution - Missense 6:28904122-28904122 - S02384 COSM5698518 c.972G>T p.T324T Substitution - coding silent 6:28904640-28904640 - TCGA-EI-6917-01 COSM3430421 c.481C>T p.R161W Substitution - Missense 6:28921927-28921927 - TCGA-BS-A0UV-01 COSM1077175 c.543G>A p.K181K Substitution - coding silent 6:28920216-28920216 - HCT8 COSM4625740 c.60G>A p.L20L Substitution - coding silent 6:28923573-28923573 - HCC14T COSM1621344 c.927A>G p.R309R Substitution - coding silent 6:28907255-28907255 - T96 COSM4736012 c.951C>T p.D317D Substitution - coding silent 6:28904661-28904661 - LUAD-RT-S01487 COSM377964 c.291G>C p.E97D Substitution - Missense 6:28923342-28923342 - RK195_C01 COSM3745111 c.1316T>G p.F439C Substitution - Missense 6:28904296-28904296 - TCGA-BF-A3DL-01 COSM4904857 c.588T>A p.H196Q Substitution - Missense 6:28920171-28920171 - TCGA-A6-6653-01 COSM1442839 c.27C>T p.C9C Substitution - coding silent 6:28923606-28923606 - HCC14 COSM1621344 c.927A>G p.R309R Substitution - coding silent 6:28907255-28907255 - HCC5 COSM3662334 c.1490G>T p.G497V Substitution - Missense 6:28904122-28904122 - TCGA-FD-A3SS-01 COSM3777424 c.1133G>A p.G378E Substitution - Missense 6:28904479-28904479 - TCGA-24-2290-01 COSM69025 c.1024delT p.Y342fs*34 Deletion - Frameshift 6:28904588-28904588 - TCGA-ER-A2NB-01 COSM3623856 c.1519C>G p.H507D Substitution - Missense 6:28904093-28904093 - TCGA-BH-A18G-01 COSM3829915 c.911A>G p.K304R Substitution - Missense 6:28908816-28908816 - S00936 COSM316134 c.658A>G p.T220A Substitution - Missense 6:28920101-28920101 - TCGA-CC-A7IK-01 COSM4925064 c.847A>T p.K283* Substitution - Nonsense 6:28909012-28909012 - J88_T COSM3948928 c.786G>C p.R262S Substitution - Missense 6:28909073-28909073 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.440382 6p22 602165

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C IntronicSNV . c.920-572T>G 6 28875611 MB A C Missense p.F474C c.1421T>G 6 28871968 NSCLC A - Frameshift p.Y342Tfs*34 c.1024delT 6 28872365 OV AGA - InFrameDeletion p.F449delF c.1346_1348delTCT 6 28872041 STAD A G Missense p.V502A c.1505T>C 6 28871884 UCEC A T Missense p.H196Q c.588T>A 6 28887948 CM A T Synonymous p.P266P c.798T>A 6 28876838 COREAD C A Missense p.G369W c.1105G>T 6 28872284 CM C A Missense p.V360F c.1078G>T 6 28872311 LUAD C A Missense p.V436L c.1306G>T 6 28872083 CM C A Missense p.W267C c.801G>T 6 28876835 LUAD CG AT Missense p.S479Y c.1436_1437delinsAT 6 28871952 CM C G Missense p.D301H c.901G>C 6 28876603 SCLC C T IntronicSNV . c.946+948G>A 6 28874065 DLBCL C T Missense p.A167T c.499G>A 6 28889686 BLCA C T Missense p.R435Q c.1304G>A 6 28872085 STAD C T Synonymous p.E195E c.585G>A 6 28887951 CM G A IntronicSNV . c.946+46C>T 6 28874967 CM G A Missense p.P486S c.1456C>T 6 28871933 HNSC G A Missense p.R336W c.1006C>T 6 28872383 HNSC G A Missense p.T288M c.863C>T 6 28876773 STAD G A Nonsense p.Q306* c.916C>T 6 28876588 CM G A Synonymous p.I305I c.915C>T 6 28876589 CM G A Synonymous p.I330I c.990C>T 6 28872399 CM G A Synonymous p.P428P c.1284C>T 6 28872105 CM G A Synonymous p.R42R c.126C>T 6 28891284 BLCA G A Synonymous p.S328S c.984C>T 6 28872405 CM G A Synonymous p.T175T c.525C>T 6 28888011 CM G C Missense p.H507D c.1519C>G 6 28871870 CM G C Missense p.L487V c.1459C>G 6 28871930 HNSC G C Missense p.P402R c.1205C>G 6 28872184 LUAD G C Missense p.T511S c.1532C>G 6 28871857 HNSC G - Frameshift p.D148Tfs*3 c.441delC 6 28889744 CM GG AA Missense p.S192F c.575_576delinsTT 6 28887960 CM G T Missense p.P432Q c.1295C>A 6 28872094 STAD G T Nonsense p.Y106* c.318C>A 6 28891092 ESCA T A Missense p.D301V c.902A>T 6 28876602 HNSC T C Missense p.T220A c.658A>G 6 28887878 SCLC T C Synonymous p.P423P c.1269A>G 6 28872120 COREAD