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 20 61510599 61510599 + Missense_Mutation SNP C C T TCGA-OR-A5JQ-01A-11D-A29I-10 TCGA-OR-A5JQ-10A-01D-A29L-10 g.chr20:61510599C>T c.6709G>A c.(6709-6711)Gcc>Acc p.A2237T ACC 20 61511207 61511207 + Frame_Shift_Del DEL G G - TCGA-PK-A5HB-01A-11D-A29I-10 TCGA-PK-A5HB-11A-11D-A29L-10 g.chr20:61511207delG c.6101delC c.(6100-6102)ccgfs p.P2034fs ACC 20 61512420 61512420 + Missense_Mutation SNP C C T TCGA-OR-A5JL-01A-11D-A29I-10 TCGA-OR-A5JL-10A-01D-A29L-10 g.chr20:61512420C>T c.4888G>A c.(4888-4890)Gag>Aag p.E1630K ACC 20 61512424 61512424 + Silent SNP C C T TCGA-OR-A5KW-01A-11D-A29I-10 TCGA-OR-A5KW-10A-01D-A29L-10 g.chr20:61512424C>T c.4884G>A c.(4882-4884)ggG>ggA p.G1628G ACC 20 61512594 61512594 + Nonsense_Mutation SNP C C A TCGA-OR-A5KB-01A-11D-A30A-10 TCGA-OR-A5KB-11A-11D-A30A-10 g.chr20:61512594C>A c.4714G>T c.(4714-4716)Gag>Tag p.E1572* ACC 20 61522425 61522425 + Missense_Mutation SNP C C T TCGA-OR-A5J5-01A-11D-A29I-10 TCGA-OR-A5J5-10A-01D-A29L-10 g.chr20:61522425C>T c.3428G>A c.(3427-3429)cGt>cAt p.R1143H ACC 20 61537287 61537287 + Missense_Mutation SNP C C G TCGA-OR-A5JV-01A-11D-A29I-10 TCGA-OR-A5JV-10A-01D-A29L-10 g.chr20:61537287C>G c.1540G>C c.(1540-1542)Gta>Cta p.V514L BLCA 20 61510942 61510942 + Silent SNP G G A TCGA-PQ-A6FI-01A-11D-A31L-08 TCGA-PQ-A6FI-10A-01D-A31J-08 g.chr20:61510942G>A c.6366C>T c.(6364-6366)aaC>aaT p.N2122N BLCA 20 61510964 61510964 + Missense_Mutation SNP C C T TCGA-XF-A9SY-01A-21D-A42E-08 TCGA-XF-A9SY-10A-01D-A42H-08 g.chr20:61510964C>T c.6344G>A c.(6343-6345)aGa>aAa p.R2115K BLCA 20 61510987 61510987 + Silent SNP G G A TCGA-XF-A9T8-01A-11D-A391-08 TCGA-XF-A9T8-10A-01D-A394-08 g.chr20:61510987G>A c.6321C>T c.(6319-6321)ggC>ggT p.G2107G BLCA 20 61511301 61511301 + Missense_Mutation SNP C C G TCGA-FD-A3B6-01A-21D-A20D-08 TCGA-FD-A3B6-10A-01D-A20D-08 g.chr20:61511301C>G c.6007G>C c.(6007-6009)Gag>Cag p.E2003Q BLCA 20 61511415 61511415 + Nonsense_Mutation SNP G G A TCGA-G2-A2EC-01A-11D-A17V-08 TCGA-G2-A2EC-10A-01D-A17V-08 g.chr20:61511415G>A c.5893C>T c.(5893-5895)Cag>Tag p.Q1965* BLCA 20 61511563 61511563 + Missense_Mutation SNP C C G TCGA-XF-A9T5-01A-11D-A42E-08 TCGA-XF-A9T5-10A-01D-A42H-08 g.chr20:61511563C>G c.5745G>C c.(5743-5745)caG>caC p.Q1915H BLCA 20 61511778 61511778 + Missense_Mutation SNP C C G TCGA-G2-AA3D-01A-11D-A391-08 TCGA-G2-AA3D-10A-01D-A394-08 g.chr20:61511778C>G c.5530G>C c.(5530-5532)Gaa>Caa p.E1844Q BLCA 20 61511837 61511837 + Missense_Mutation SNP C C G TCGA-DK-A1A6-01A-11D-A13W-08 TCGA-DK-A1A6-10A-01D-A13W-08 g.chr20:61511837C>G c.5471G>C c.(5470-5472)aGa>aCa p.R1824T BLCA 20 61511837 61511837 + Missense_Mutation SNP C C T TCGA-SY-A9G5-01A-11D-A38G-08 TCGA-SY-A9G5-10A-01D-A38J-08 g.chr20:61511837C>T c.5471G>A c.(5470-5472)aGa>aAa p.R1824K BLCA 20 61511882 61511882 + Missense_Mutation SNP G G T TCGA-G2-A2EC-01A-11D-A17V-08 TCGA-G2-A2EC-10A-01D-A17V-08 g.chr20:61511882G>T c.5426C>A c.(5425-5427)tCc>tAc p.S1809Y BLCA 20 61511899 61511899 + Missense_Mutation SNP C C A TCGA-SY-A9G5-01A-11D-A38G-08 TCGA-SY-A9G5-10A-01D-A38J-08 g.chr20:61511899C>A c.5409G>T c.(5407-5409)caG>caT p.Q1803H BLCA 20 61511899 61511899 + Missense_Mutation SNP C C G TCGA-K4-A5RJ-01A-11D-A289-08 TCGA-K4-A5RJ-10A-01D-A289-08 g.chr20:61511899C>G c.5409G>C c.(5407-5409)caG>caC p.Q1803H BLCA 20 61512150 61512150 + Missense_Mutation SNP C C T TCGA-DK-A2I4-01A-11D-A21A-08 TCGA-DK-A2I4-10A-01D-A21A-08 g.chr20:61512150C>T c.5158G>A c.(5158-5160)Gag>Aag p.E1720K BLCA 20 61512241 61512241 + Silent SNP C C T TCGA-UY-A9PE-01A-11D-A38G-08 TCGA-UY-A9PE-10A-01D-A38J-08 g.chr20:61512241C>T c.5067G>A c.(5065-5067)gcG>gcA p.A1689A BLCA 20 61512313 61512313 + Silent SNP G G A TCGA-XF-AAN1-01A-31D-A42E-08 TCGA-XF-AAN1-10A-01D-A42H-08 g.chr20:61512313G>A c.4995C>T c.(4993-4995)tgC>tgT p.C1665C BLCA 20 61512446 61512446 + Missense_Mutation SNP G G A TCGA-G2-A2EC-01A-11D-A17V-08 TCGA-G2-A2EC-10A-01D-A17V-08 g.chr20:61512446G>A c.4862C>T c.(4861-4863)tCg>tTg p.S1621L BLCA 20 61512478 61512478 + Missense_Mutation SNP C C G TCGA-GU-A764-01A-11D-A34U-08 TCGA-GU-A764-10B-01D-A34X-08 g.chr20:61512478C>G c.4830G>C c.(4828-4830)gaG>gaC p.E1610D BLCA 20 61512603 61512603 + Missense_Mutation SNP C C T TCGA-XF-A9SM-01A-11D-A42E-08 TCGA-XF-A9SM-10A-01D-A42H-08 g.chr20:61512603C>T c.4705G>A c.(4705-4707)Gag>Aag p.E1569K BLCA 20 61512799 61512799 + Silent SNP C C T TCGA-GV-A3JX-01A-11D-A20D-08 TCGA-GV-A3JX-10A-01D-A20D-08 g.chr20:61512799C>T c.4509G>A c.(4507-4509)caG>caA p.Q1503Q BLCA 20 61512978 61512978 + Silent SNP G G A TCGA-G2-A2EC-01A-11D-A17V-08 TCGA-G2-A2EC-10A-01D-A17V-08 g.chr20:61512978G>A c.4330C>T c.(4330-4332)Ctg>Ttg p.L1444L BLCA 20 61512984 61512984 + Missense_Mutation SNP C C G TCGA-DK-A3X1-01A-12D-A22Z-08 TCGA-DK-A3X1-10A-01D-A22Z-08 g.chr20:61512984C>G c.4324G>C c.(4324-4326)Gat>Cat p.D1442H BLCA 20 61513002 61513002 + Nonsense_Mutation SNP C C A TCGA-XF-A9SY-01A-21D-A42E-08 TCGA-XF-A9SY-10A-01D-A42H-08 g.chr20:61513002C>A c.4306G>T c.(4306-4308)Gaa>Taa p.E1436* BLCA 20 61513017 61513017 + Missense_Mutation SNP C C T TCGA-UY-A9PE-01A-11D-A38G-08 TCGA-UY-A9PE-10A-01D-A38J-08 g.chr20:61513017C>T c.4291G>A c.(4291-4293)Gag>Aag p.E1431K BLCA 20 61513072 61513072 + Missense_Mutation SNP C C G TCGA-DK-A3IL-01A-11D-A20D-08 TCGA-DK-A3IL-10A-01D-A20D-08 g.chr20:61513072C>G c.4236G>C c.(4234-4236)agG>agC p.R1412S BLCA 20 61513083 61513083 + Missense_Mutation SNP C C T TCGA-FD-A3SO-01A-11D-A22Z-08 TCGA-FD-A3SO-10A-01D-A22Z-08 g.chr20:61513083C>T c.4225G>A c.(4225-4227)Gag>Aag p.E1409K BLCA 20 61513083 61513083 + Missense_Mutation SNP C C T TCGA-FD-A6TG-01A-11D-A32B-08 TCGA-FD-A6TG-10A-01D-A329-08 g.chr20:61513083C>T c.4225G>A c.(4225-4227)Gag>Aag p.E1409K BLCA 20 61513097 61513097 + Missense_Mutation SNP C C T TCGA-5N-A9KM-01A-11D-A42E-08 TCGA-5N-A9KM-10A-01D-A42H-08 g.chr20:61513097C>T c.4211G>A c.(4210-4212)cGa>cAa p.R1404Q BLCA 20 61513152 61513152 + Missense_Mutation SNP C C T TCGA-UY-A78K-01A-11D-A339-08 TCGA-UY-A78K-10A-01D-A339-08 g.chr20:61513152C>T c.4156G>A c.(4156-4158)Gac>Aac p.D1386N BLCA 20 61513517 61513517 + Missense_Mutation SNP G G A TCGA-KQ-A41N-01A-11D-A339-08 TCGA-KQ-A41N-10D-01D-A339-08 g.chr20:61513517G>A c.3791C>T c.(3790-3792)cCg>cTg p.P1264L BLCA 20 61513532 61513532 + Missense_Mutation SNP C C A TCGA-DK-A3IK-01A-32D-A21A-08 TCGA-DK-A3IK-10A-01D-A21A-08 g.chr20:61513532C>A c.3776G>T c.(3775-3777)gGg>gTg p.G1259V BLCA 20 61522433 61522433 + Silent SNP G G A TCGA-FD-A62P-01A-32D-A30E-08 TCGA-FD-A62P-10A-01D-A30H-08 g.chr20:61522433G>A c.3420C>T c.(3418-3420)ttC>ttT p.F1140F BLCA 20 61524224 61524224 + Missense_Mutation SNP C C G TCGA-DK-A3WW-01A-22D-A23M-08 TCGA-DK-A3WW-10A-01D-A23K-08 g.chr20:61524224C>G c.3192G>C c.(3190-3192)caG>caC p.Q1064H BLCA 20 61525040 61525040 + Missense_Mutation SNP C C T TCGA-E7-A541-01A-11D-A26M-08 TCGA-E7-A541-10A-01D-A26K-08 g.chr20:61525040C>T c.3079G>A c.(3079-3081)Gtt>Att p.V1027I BLCA 20 61525162 61525162 + Missense_Mutation SNP G G A TCGA-XF-A9T3-01A-11D-A42E-08 TCGA-XF-A9T3-10A-01D-A42H-08 g.chr20:61525162G>A c.2957C>T c.(2956-2958)cCa>cTa p.P986L BLCA 20 61525370 61525370 + Missense_Mutation SNP C C G TCGA-BL-A5ZZ-01A-31D-A30E-08 TCGA-BL-A5ZZ-10A-01D-A30H-08 g.chr20:61525370C>G c.2749G>C c.(2749-2751)Gaa>Caa p.E917Q BLCA 20 61525505 61525506 + Frame_Shift_Ins INS - - T TCGA-G2-AA3D-01A-11D-A391-08 TCGA-G2-AA3D-10A-01D-A394-08 g.chr20:61525505_61525506insT c.2613_2614insA c.(2611-2616)aaacaafs p.Q872fs BLCA 20 61525841 61525841 + Silent SNP G G A TCGA-CF-A3MF-01A-12D-A21A-08 TCGA-CF-A3MF-10A-01D-A21A-08 g.chr20:61525841G>A c.2496C>T c.(2494-2496)gtC>gtT p.V832V BLCA 20 61525865 61525865 + Silent SNP C C T TCGA-LC-A66R-01A-41D-A30E-08 TCGA-LC-A66R-10A-01D-A30H-08 g.chr20:61525865C>T c.2472G>A c.(2470-2472)aaG>aaA p.K824K BLCA 20 61526264 61526264 + Silent SNP C C T TCGA-BL-A5ZZ-01A-31D-A30E-08 TCGA-BL-A5ZZ-10A-01D-A30H-08 g.chr20:61526264C>T c.2334G>A c.(2332-2334)gtG>gtA p.V778V BLCA 20 61526407 61526407 + Silent SNP C C T TCGA-CF-A9FF-01A-11D-A38G-08 TCGA-CF-A9FF-10A-01D-A38J-08 g.chr20:61526407C>T c.2325G>A c.(2323-2325)gcG>gcA p.A775A BLCA 20 61526467 61526467 + Silent SNP C C G TCGA-E7-A7XN-01A-11D-A34U-08 TCGA-E7-A7XN-10A-01D-A34X-08 g.chr20:61526467C>G c.2265G>C c.(2263-2265)gtG>gtC p.V755V BLCA 20 61526493 61526493 + Missense_Mutation SNP C C G TCGA-G2-A2EO-01A-11D-A17V-08 TCGA-G2-A2EO-11A-21D-A17V-08 g.chr20:61526493C>G c.2239G>C c.(2239-2241)Gag>Cag p.E747Q BLCA 20 61527666 61527666 + Missense_Mutation SNP A A T TCGA-FT-A3EE-01A-11D-A202-08 TCGA-FT-A3EE-10A-01D-A202-08 g.chr20:61527666A>T c.2133T>A c.(2131-2133)ttT>ttA p.F711L BLCA 20 61527713 61527713 + Missense_Mutation SNP C C T TCGA-E7-A7XN-01A-11D-A34U-08 TCGA-E7-A7XN-10A-01D-A34X-08 g.chr20:61527713C>T c.2086G>A c.(2086-2088)Gaa>Aaa p.E696K BLCA 20 61528239 61528239 + Silent SNP G G A TCGA-GV-A6ZA-01A-12D-A339-08 TCGA-GV-A6ZA-10A-01D-A339-08 g.chr20:61528239G>A c.1698C>T c.(1696-1698)ctC>ctT p.L566L BLCA 20 61537196 61537196 + Intron SNP G G A TCGA-DK-A6B6-01A-11D-A30E-08 TCGA-DK-A6B6-10A-01D-A30H-08 g.chr20:61537196G>A BLCA 20 61537309 61537309 + Silent SNP C C A TCGA-FD-A6TE-01A-12D-A339-08 TCGA-FD-A6TE-10A-21D-A339-08 g.chr20:61537309C>A c.1518G>T c.(1516-1518)gcG>gcT p.A506A BLCA 20 61537316 61537316 + Missense_Mutation SNP G G A TCGA-GD-A2C5-01A-12D-A17V-08 TCGA-GD-A2C5-10A-01D-A17V-08 g.chr20:61537316G>A c.1511C>T c.(1510-1512)tCg>tTg p.S504L BLCA 20 61537421 61537421 + Missense_Mutation SNP C C G TCGA-XF-A9ST-01A-11D-A42E-08 TCGA-XF-A9ST-10A-01D-A42H-08 g.chr20:61537421C>G c.1406G>C c.(1405-1407)aGa>aCa p.R469T BLCA 20 61541160 61541160 + Missense_Mutation SNP G G A TCGA-GV-A3QK-01B-11D-A23M-08 TCGA-GV-A3QK-10A-01D-A23K-08 g.chr20:61541160G>A c.1052C>T c.(1051-1053)aCa>aTa p.T351I BLCA 20 61541311 61541311 + Missense_Mutation SNP C C T TCGA-DK-A3IT-01A-31D-A20D-08 TCGA-DK-A3IT-10A-01D-A20D-08 g.chr20:61541311C>T c.901G>A c.(901-903)Gag>Aag p.E301K BLCA 20 61542370 61542370 + Missense_Mutation SNP C C T TCGA-XF-AAMG-01A-11D-A42E-08 TCGA-XF-AAMG-10A-01D-A42H-08 g.chr20:61542370C>T c.595G>A c.(595-597)Gag>Aag p.E199K BLCA 20 61542646 61542646 + Missense_Mutation SNP C C A TCGA-PQ-A6FN-01A-11D-A31L-08 TCGA-PQ-A6FN-10A-01D-A31J-08 g.chr20:61542646C>A c.319G>T c.(319-321)Gcc>Tcc p.A107S BLCA 20 61542751 61542751 + Missense_Mutation SNP C C T TCGA-FD-A62O-01A-11D-A30E-08 TCGA-FD-A62O-10A-01D-A30H-08 g.chr20:61542751C>T c.214G>A c.(214-216)Gag>Aag p.E72K BLCA 20 61542853 61542853 + Missense_Mutation SNP C C T TCGA-KQ-A41R-01A-21D-A34U-08 TCGA-KQ-A41R-10G-01D-A34X-08 g.chr20:61542853C>T c.112G>A c.(112-114)Gag>Aag p.E38K BRCA 20 61512736 61512736 + Silent SNP T T G TCGA-BH-A0WA-01A-11D-A10G-09 TCGA-BH-A0WA-10A-01D-A117-09 g.chr20:61512736T>G c.4572A>C c.(4570-4572)ccA>ccC p.P1524P BRCA 20 61512792 61512792 + Missense_Mutation SNP C C T TCGA-A2-A0YG-01A-21D-A10G-09 TCGA-A2-A0YG-10A-01D-A10G-09 g.chr20:61512792C>T c.4516G>A c.(4516-4518)Gcc>Acc p.A1506T BRCA 20 61513156 61513156 + Silent SNP T T C TCGA-A8-A07R-01A-21W-A050-09 TCGA-A8-A07R-10B-01D-A047-09 g.chr20:61513156T>C c.4152A>G c.(4150-4152)ccA>ccG p.P1384P BRCA 20 61522371 61522371 + Missense_Mutation SNP A A C TCGA-EW-A1PB-01A-11D-A142-09 TCGA-EW-A1PB-10A-01D-A142-09 g.chr20:61522371A>C c.3482T>G c.(3481-3483)cTg>cGg p.L1161R BRCA 20 61523338 61523338 + Splice_Site SNP C C G TCGA-C8-A132-01A-31D-A10Y-09 TCGA-C8-A132-10A-01D-A110-09 g.chr20:61523338C>G c.e14+1 BRCA 20 61524224 61524224 + Silent SNP C C T TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr20:61524224C>T c.3192G>A c.(3190-3192)caG>caA p.Q1064Q BRCA 20 61525826 61525826 + Missense_Mutation SNP C C G TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr20:61525826C>G c.2511G>C c.(2509-2511)ttG>ttC p.L837F BRCA 20 61537437 61537438 + Frame_Shift_Ins INS - - T TCGA-AN-A04C-01A-21W-A050-09 TCGA-AN-A04C-10A-01D-A047-09 g.chr20:61537437_61537438insT c.1389_1390insA c.(1387-1392)atctctfs p.S464fs BRCA 20 61537438 61537438 + Silent SNP G G T TCGA-AN-A046-01A-21W-A050-09 TCGA-AN-A046-10A-01W-A055-09 g.chr20:61537438G>T c.1389C>A c.(1387-1389)atC>atA p.I463I BRCA 20 61542181 61542181 + Missense_Mutation SNP C C T TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr20:61542181C>T c.784G>A c.(784-786)Gag>Aag p.E262K BRCA 20 61542268 61542268 + Missense_Mutation SNP C C T TCGA-A7-A0D9-01A-31W-A071-09 TCGA-A7-A0D9-11A-53W-A100-09 g.chr20:61542268C>T c.697G>A c.(697-699)Gac>Aac p.D233N BRCA 20 61542482 61542482 + Silent SNP C C T TCGA-A7-A0D9-01A-31W-A071-09 TCGA-A7-A0D9-11A-53W-A100-09 g.chr20:61542482C>T c.483G>A c.(481-483)ttG>ttA p.L161L BRCA 20 61542562 61542562 + Nonsense_Mutation SNP G G A TCGA-AO-A128-01A-11D-A10M-09 TCGA-AO-A128-10A-01D-A10M-09 g.chr20:61542562G>A c.403C>T c.(403-405)Cga>Tga p.R135* BRCA 20 61542600 61542600 + Missense_Mutation SNP C C G TCGA-A8-A09G-01A-21W-A019-09 TCGA-A8-A09G-10A-01W-A021-09 g.chr20:61542600C>G c.365G>C c.(364-366)aGa>aCa p.R122T BRCA 20 61542836 61542836 + Silent SNP C C T TCGA-D8-A1XK-01A-21D-A14K-09 TCGA-D8-A1XK-10A-01D-A14K-09 g.chr20:61542836C>T c.129G>A c.(127-129)gcG>gcA p.A43A BRCA 20 61542888 61542888 + Missense_Mutation SNP G G A TCGA-E2-A1L7-01A-11D-A142-09 TCGA-E2-A1L7-10A-01D-A142-09 g.chr20:61542888G>A c.77C>T c.(76-78)aCa>aTa p.T26I CESC 20 61510621 61510621 + Silent SNP C C T TCGA-DS-A5RQ-01A-11D-A28B-09 TCGA-DS-A5RQ-10A-01D-A28E-09 g.chr20:61510621C>T c.6687G>A c.(6685-6687)tcG>tcA p.S2229S CESC 20 61511181 61511181 + Missense_Mutation SNP C C T TCGA-EA-A439-01A-11D-A243-09 TCGA-EA-A439-10A-01D-A243-09 g.chr20:61511181C>T c.6127G>A c.(6127-6129)Gag>Aag p.E2043K CESC 20 61512312 61512312 + Missense_Mutation SNP C C T TCGA-Q1-A5R2-01A-11D-A28B-09 TCGA-Q1-A5R2-10A-01D-A28E-09 g.chr20:61512312C>T c.4996G>A c.(4996-4998)Ggc>Agc p.G1666S CESC 20 61512828 61512828 + Missense_Mutation SNP C C G TCGA-Q1-A6DT-01A-11D-A32I-09 TCGA-Q1-A6DT-10A-01D-A32I-09 g.chr20:61512828C>G c.4480G>C c.(4480-4482)Gag>Cag p.E1494Q CESC 20 61513055 61513055 + Missense_Mutation SNP G G T TCGA-MU-A5YI-01A-11D-A32I-09 TCGA-MU-A5YI-10A-01D-A32I-09 g.chr20:61513055G>T c.4253C>A c.(4252-4254)gCa>gAa p.A1418E CESC 20 61525016 61525016 + Splice_Site SNP A A T TCGA-EK-A3GK-01A-11D-A20U-09 TCGA-EK-A3GK-10A-01D-A20U-09 g.chr20:61525016A>T c.e12+1 CESC 20 61525382 61525382 + Missense_Mutation SNP C C T TCGA-MY-A5BD-01A-11D-A26G-09 TCGA-MY-A5BD-10A-01D-A26G-09 g.chr20:61525382C>T c.2737G>A c.(2737-2739)Gag>Aag p.E913K CESC 20 61526236 61526236 + Missense_Mutation SNP C C T TCGA-IR-A3LA-01A-11D-A22X-09 TCGA-IR-A3LA-10A-01D-A22X-09 g.chr20:61526236C>T c.2362G>A c.(2362-2364)Gaa>Aaa p.E788K CESC 20 61527728 61527728 + Missense_Mutation SNP C C G TCGA-C5-A1MF-01A-11D-A13W-08 TCGA-C5-A1MF-10A-01D-A13W-08 g.chr20:61527728C>G c.2071G>C c.(2071-2073)Gac>Cac p.D691H CESC 20 61542823 61542823 + Silent SNP G G A TCGA-DS-A0VN-01A-21D-A10S-08 TCGA-DS-A0VN-10A-01D-A10S-08 g.chr20:61542823G>A c.142C>T c.(142-144)Ctg>Ttg p.L48L CHOL 20 61512147 61512147 + Missense_Mutation SNP C C G TCGA-W5-AA2T-01A-12D-A417-09 TCGA-W5-AA2T-10A-01D-A41A-09 g.chr20:61512147C>G c.5161G>C c.(5161-5163)Ggg>Cgg p.G1721R COAD 20 61510681 61510681 + Silent SNP G G A TCGA-CM-4752-01A-01D-1408-10 TCGA-CM-4752-10A-01D-1408-10 g.chr20:61510681G>A c.6627C>T c.(6625-6627)cgC>cgT p.R2209R COAD 20 61510712 61510712 + Missense_Mutation SNP C C T TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr20:61510712C>T c.6596G>A c.(6595-6597)cGa>cAa p.R2199Q COAD 20 61510857 61510857 + Missense_Mutation SNP G G A TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr20:61510857G>A c.6451C>T c.(6451-6453)Cgg>Tgg p.R2151W COAD 20 61510959 61510959 + Missense_Mutation SNP G G A TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr20:61510959G>A c.6349C>T c.(6349-6351)Cgc>Tgc p.R2117C COAD 20 61511050 61511050 + Missense_Mutation SNP C C A TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr20:61511050C>A c.6258G>T c.(6256-6258)agG>agT p.R2086S COAD 20 61511242 61511242 + Silent SNP G G A TCGA-CM-6161-01A-11D-1650-10 TCGA-CM-6161-10A-01D-1650-10 g.chr20:61511242G>A c.6066C>T c.(6064-6066)ggC>ggT p.G2022G COAD 20 61511257 61511257 + Missense_Mutation SNP C C A TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr20:61511257C>A c.6051G>T c.(6049-6051)caG>caT p.Q2017H COAD 20 61511496 61511496 + Missense_Mutation SNP G G A TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr20:61511496G>A c.5812C>T c.(5812-5814)Cgg>Tgg p.R1938W COAD 20 61511656 61511656 + Silent SNP G G A TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr20:61511656G>A c.5652C>T c.(5650-5652)ggC>ggT p.G1884G COAD 20 61511929 61511929 + Silent SNP T T C TCGA-A6-5666-01A-01D-1650-10 TCGA-A6-5666-10A-01D-1650-10 g.chr20:61511929T>C c.5379A>G c.(5377-5379)cgA>cgG p.R1793R COAD 20 61512095 61512095 + Missense_Mutation SNP G G A TCGA-AY-6196-01A-11D-1719-10 TCGA-AY-6196-10A-01D-1719-10 g.chr20:61512095G>A c.5213C>T c.(5212-5214)cCa>cTa p.P1738L COAD 20 61512102 61512102 + Missense_Mutation SNP G G A TCGA-AY-6196-01A-11D-1719-10 TCGA-AY-6196-10A-01D-1719-10 g.chr20:61512102G>A c.5206C>T c.(5206-5208)Ctc>Ttc p.L1736F COAD 20 61512784 61512784 + Silent SNP C C T TCGA-CA-5254-01A-21D-1835-10 TCGA-CA-5254-10A-01D-1835-10 g.chr20:61512784C>T c.4524G>A c.(4522-4524)ggG>ggA p.G1508G COAD 20 61512998 61512998 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr20:61512998G>A c.4310C>T c.(4309-4311)gCg>gTg p.A1437V COAD 20 61513092 61513092 + Missense_Mutation SNP G G A TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr20:61513092G>A c.4216C>T c.(4216-4218)Cgg>Tgg p.R1406W COAD 20 61513155 61513155 + Missense_Mutation SNP A A G TCGA-AA-3821-01A-01W-0995-10 TCGA-AA-3821-10A-01W-0995-10 g.chr20:61513155A>G c.4153T>C c.(4153-4155)Tac>Cac p.Y1385H COAD 20 61513370 61513370 + Missense_Mutation SNP G G A TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr20:61513370G>A c.3938C>T c.(3937-3939)cCg>cTg p.P1313L COAD 20 61513527 61513527 + Missense_Mutation SNP G G A TCGA-G4-6304-01A-11D-1924-10 TCGA-G4-6304-10A-01D-1924-10 g.chr20:61513527G>A c.3781C>T c.(3781-3783)Ccg>Tcg p.P1261S COAD 20 61513681 61513681 + Silent SNP G G A TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr20:61513681G>A c.3627C>T c.(3625-3627)gaC>gaT p.D1209D COAD 20 61522306 61522306 + Intron SNP G G A TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr20:61522306G>A COAD 20 61522323 61522323 + Missense_Mutation SNP A A C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr20:61522323A>C c.3530T>G c.(3529-3531)tTt>tGt p.F1177C COAD 20 61522460 61522460 + Silent SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr20:61522460G>A c.3393C>T c.(3391-3393)gtC>gtT p.V1131V COAD 20 61523352 61523352 + Missense_Mutation SNP G G A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr20:61523352G>A c.3332C>T c.(3331-3333)tCt>tTt p.S1111F COAD 20 61523414 61523414 + Silent SNP T T G TCGA-AA-A01Q-01A-01W-A005-10 TCGA-AA-A01Q-10A-01W-A005-10 g.chr20:61523414T>G c.3270A>C c.(3268-3270)acA>acC p.T1090T COAD 20 61525181 61525181 + Missense_Mutation SNP C C T TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr20:61525181C>T c.2938G>A c.(2938-2940)Gcc>Acc p.A980T COAD 20 61525363 61525364 + Missense_Mutation DNP GC GC AT TCGA-AA-A01K-01A-01W-A00E-09 TCGA-AA-A01K-10A-01W-A00E-09 g.chr20:61525363_61525364GC>AT c.2755_2756GC>AT c.(2755-2757)GCt>ATt p.A919I COAD 20 61525830 61525830 + Missense_Mutation SNP A A G TCGA-CK-5915-01A-11D-1650-10 TCGA-CK-5915-10A-01D-1650-10 g.chr20:61525830A>G c.2507T>C c.(2506-2508)aTg>aCg p.M836T COAD 20 61526171 61526171 + Silent SNP C C A TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr20:61526171C>A c.2427G>T c.(2425-2427)tcG>tcT p.S809S COAD 20 61526425 61526425 + Silent SNP C C T TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr20:61526425C>T c.2307G>A c.(2305-2307)acG>acA p.T769T COAD 20 61526505 61526505 + Missense_Mutation SNP G G A TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr20:61526505G>A c.2227C>T c.(2227-2229)Cgt>Tgt p.R743C COAD 20 61527666 61527666 + Frame_Shift_Del DEL A A - TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr20:61527666delA c.2133delT c.(2131-2133)tttfs p.F711fs COAD 20 61527946 61527946 + Missense_Mutation SNP G G A TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr20:61527946G>A c.1991C>T c.(1990-1992)tCg>tTg p.S664L COAD 20 61527959 61527959 + Missense_Mutation SNP T T C TCGA-AA-3662-01A-01D-1719-10 TCGA-AA-3662-11A-01D-1719-10 g.chr20:61527959T>C c.1978A>G c.(1978-1980)Agt>Ggt p.S660G COAD 20 61528199 61528199 + Missense_Mutation SNP T T A TCGA-AY-6196-01A-11D-1719-10 TCGA-AY-6196-10A-01D-1719-10 g.chr20:61528199T>A c.1738A>T c.(1738-1740)Aca>Tca p.T580S COAD 20 61528256 61528256 + Missense_Mutation SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr20:61528256G>A c.1681C>T c.(1681-1683)Cct>Tct p.P561S COAD 20 61537340 61537340 + Missense_Mutation SNP G G A TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr20:61537340G>A c.1487C>T c.(1486-1488)gCa>gTa p.A496V COAD 20 61537402 61537402 + Frame_Shift_Del DEL T T - TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr20:61537402delT c.1425delA c.(1423-1425)aaafs p.K475fs COAD 20 61537415 61537415 + Missense_Mutation SNP G G T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr20:61537415G>T c.1412C>A c.(1411-1413)gCt>gAt p.A471D COAD 20 61538507 61538507 + Missense_Mutation SNP C C T TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr20:61538507C>T c.1366G>A c.(1366-1368)Ggt>Agt p.G456S COAD 20 61538606 61538606 + Missense_Mutation SNP C C T TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr20:61538606C>T c.1267G>A c.(1267-1269)Gca>Aca p.A423T COAD 20 61538626 61538626 + Missense_Mutation SNP T T C TCGA-AA-3712-01A-21D-1719-10 TCGA-AA-3712-11A-01D-1719-10 g.chr20:61538626T>C c.1247A>G c.(1246-1248)gAc>gGc p.D416G COAD 20 61538701 61538701 + Missense_Mutation SNP G G A TCGA-AA-3821-01A-01W-0995-10 TCGA-AA-3821-10A-01W-0995-10 g.chr20:61538701G>A c.1172C>T c.(1171-1173)gCg>gTg p.A391V COAD 20 61538704 61538704 + Missense_Mutation SNP T T G TCGA-AA-3877-01A-01W-0995-10 TCGA-AA-3877-10A-01W-0995-10 g.chr20:61538704T>G c.1169A>C c.(1168-1170)gAg>gCg p.E390A COAD 20 61542279 61542279 + Missense_Mutation SNP G G A TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr20:61542279G>A c.686C>T c.(685-687)gCt>gTt p.A229V COAD 20 61542332 61542332 + Silent SNP G G A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr20:61542332G>A c.633C>T c.(631-633)ggC>ggT p.G211G COADREAD 20 61510681 61510681 + Silent SNP G G A TCGA-CM-4752-01A-01D-1408-10 TCGA-CM-4752-10A-01D-1408-10 g.chr20:61510681G>A c.6627C>T c.(6625-6627)cgC>cgT p.R2209R COADREAD 20 61510712 61510712 + Missense_Mutation SNP C C T TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr20:61510712C>T c.6596G>A c.(6595-6597)cGa>cAa p.R2199Q COADREAD 20 61510857 61510857 + Missense_Mutation SNP G G A TCGA-CK-5913-01A-11D-1650-10 TCGA-CK-5913-10A-01D-1650-10 g.chr20:61510857G>A c.6451C>T c.(6451-6453)Cgg>Tgg p.R2151W COADREAD 20 61510959 61510959 + Missense_Mutation SNP G G A TCGA-D5-6930-01A-11D-1924-10 TCGA-D5-6930-10A-01D-1924-10 g.chr20:61510959G>A c.6349C>T c.(6349-6351)Cgc>Tgc p.R2117C COADREAD 20 61511050 61511050 + Missense_Mutation SNP C C A TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr20:61511050C>A c.6258G>T c.(6256-6258)agG>agT p.R2086S COADREAD 20 61511242 61511242 + Silent SNP G G A TCGA-CM-6161-01A-11D-1650-10 TCGA-CM-6161-10A-01D-1650-10 g.chr20:61511242G>A c.6066C>T c.(6064-6066)ggC>ggT p.G2022G COADREAD 20 61511257 61511257 + Missense_Mutation SNP C C A TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr20:61511257C>A c.6051G>T c.(6049-6051)caG>caT p.Q2017H COADREAD 20 61511496 61511496 + Missense_Mutation SNP G G A TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr20:61511496G>A c.5812C>T c.(5812-5814)Cgg>Tgg p.R1938W COADREAD 20 61511656 61511656 + Silent SNP G G A TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr20:61511656G>A c.5652C>T c.(5650-5652)ggC>ggT p.G1884G COADREAD 20 61511660 61511660 + Missense_Mutation SNP C C A TCGA-AG-3999-01A-01W-1073-09 TCGA-AG-3999-10A-01W-1073-09 g.chr20:61511660C>A c.5648G>T c.(5647-5649)gGc>gTc p.G1883V COADREAD 20 61511929 61511929 + Silent SNP T T C TCGA-A6-5666-01A-01D-1650-10 TCGA-A6-5666-10A-01D-1650-10 g.chr20:61511929T>C c.5379A>G c.(5377-5379)cgA>cgG p.R1793R COADREAD 20 61512095 61512095 + Missense_Mutation SNP G G A TCGA-AY-6196-01A-11D-1719-10 TCGA-AY-6196-10A-01D-1719-10 g.chr20:61512095G>A c.5213C>T c.(5212-5214)cCa>cTa p.P1738L COADREAD 20 61512102 61512102 + Missense_Mutation SNP G G A TCGA-AY-6196-01A-11D-1719-10 TCGA-AY-6196-10A-01D-1719-10 g.chr20:61512102G>A c.5206C>T c.(5206-5208)Ctc>Ttc p.L1736F COADREAD 20 61512784 61512784 + Silent SNP C C T TCGA-CA-5254-01A-21D-1835-10 TCGA-CA-5254-10A-01D-1835-10 g.chr20:61512784C>T c.4524G>A c.(4522-4524)ggG>ggA p.G1508G COADREAD 20 61512998 61512998 + Missense_Mutation SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr20:61512998G>A c.4310C>T c.(4309-4311)gCg>gTg p.A1437V COADREAD 20 61513092 61513092 + Missense_Mutation SNP G G A TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr20:61513092G>A c.4216C>T c.(4216-4218)Cgg>Tgg p.R1406W COADREAD 20 61513155 61513155 + Missense_Mutation SNP A A G TCGA-AA-3821-01A-01W-0995-10 TCGA-AA-3821-10A-01W-0995-10 g.chr20:61513155A>G c.4153T>C c.(4153-4155)Tac>Cac p.Y1385H COADREAD 20 61513251 61513251 + Missense_Mutation SNP C C T TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr20:61513251C>T c.4057G>A c.(4057-4059)Ggg>Agg p.G1353R COADREAD 20 61513370 61513370 + Missense_Mutation SNP G G A TCGA-AA-3713-01A-21D-1719-10 TCGA-AA-3713-11A-01D-1719-10 g.chr20:61513370G>A c.3938C>T c.(3937-3939)cCg>cTg p.P1313L COADREAD 20 61513408 61513408 + Silent SNP A A G TCGA-CL-5918-01A-11D-1657-10 TCGA-CL-5918-10A-01D-1657-10 g.chr20:61513408A>G c.3900T>C c.(3898-3900)gcT>gcC p.A1300A COADREAD 20 61513527 61513527 + Missense_Mutation SNP G G A TCGA-G4-6304-01A-11D-1924-10 TCGA-G4-6304-10A-01D-1924-10 g.chr20:61513527G>A c.3781C>T c.(3781-3783)Ccg>Tcg p.P1261S COADREAD 20 61513681 61513681 + Silent SNP G G A TCGA-G4-6628-01A-11D-1835-10 TCGA-G4-6628-10A-01D-1835-10 g.chr20:61513681G>A c.3627C>T c.(3625-3627)gaC>gaT p.D1209D COADREAD 20 61513713 61513713 + Frame_Shift_Del DEL T T - TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr20:61513713delT c.3595delA c.(3595-3597)atcfs p.I1199fs COADREAD 20 61522306 61522306 + Intron SNP G G A TCGA-F4-6570-01A-11D-1771-10 TCGA-F4-6570-10A-01D-1771-10 g.chr20:61522306G>A COADREAD 20 61522323 61522323 + Missense_Mutation SNP A A C TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr20:61522323A>C c.3530T>G c.(3529-3531)tTt>tGt p.F1177C COADREAD 20 61522460 61522460 + Silent SNP G G A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr20:61522460G>A c.3393C>T c.(3391-3393)gtC>gtT p.V1131V COADREAD 20 61523352 61523352 + Missense_Mutation SNP G G A TCGA-AA-3510-01A-01D-1408-10 TCGA-AA-3510-11A-01D-1408-10 g.chr20:61523352G>A c.3332C>T c.(3331-3333)tCt>tTt p.S1111F COADREAD 20 61523414 61523414 + Silent SNP T T G TCGA-AA-A01Q-01A-01W-A005-10 TCGA-AA-A01Q-10A-01W-A005-10 g.chr20:61523414T>G c.3270A>C c.(3268-3270)acA>acC p.T1090T COADREAD 20 61524262 61524262 + Nonsense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr20:61524262G>A c.3154C>T c.(3154-3156)Cga>Tga p.R1052* COADREAD 20 61525181 61525181 + Missense_Mutation SNP C C T TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr20:61525181C>T c.2938G>A c.(2938-2940)Gcc>Acc p.A980T COADREAD 20 61525363 61525364 + Missense_Mutation DNP GC GC AT TCGA-AA-A01K-01A-01W-A00E-09 TCGA-AA-A01K-10A-01W-A00E-09 g.chr20:61525363_61525364GC>AT c.2755_2756GC>AT c.(2755-2757)GCt>ATt p.A919I COADREAD 20 61525830 61525830 + Missense_Mutation SNP A A G TCGA-CK-5915-01A-11D-1650-10 TCGA-CK-5915-10A-01D-1650-10 g.chr20:61525830A>G c.2507T>C c.(2506-2508)aTg>aCg p.M836T COADREAD 20 61526171 61526171 + Silent SNP C C A TCGA-CK-6746-01A-11D-1835-10 TCGA-CK-6746-10A-01D-1835-10 g.chr20:61526171C>A c.2427G>T c.(2425-2427)tcG>tcT p.S809S COADREAD 20 61526425 61526425 + Silent SNP C C T TCGA-AA-A022-01A-21W-A096-10 TCGA-AA-A022-11A-11W-A096-10 g.chr20:61526425C>T c.2307G>A c.(2305-2307)acG>acA p.T769T COADREAD 20 61526505 61526505 + Missense_Mutation SNP G G A TCGA-D5-6928-01A-11D-1924-10 TCGA-D5-6928-10A-01D-1924-10 g.chr20:61526505G>A c.2227C>T c.(2227-2229)Cgt>Tgt p.R743C COADREAD 20 61527666 61527666 + Frame_Shift_Del DEL A A - TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr20:61527666delA c.2133delT c.(2131-2133)tttfs p.F711fs COADREAD 20 61527946 61527946 + Missense_Mutation SNP G G A TCGA-CM-4743-01A-01D-1719-10 TCGA-CM-4743-10A-01D-1719-10 g.chr20:61527946G>A c.1991C>T c.(1990-1992)tCg>tTg p.S664L COADREAD 20 61527957 61527957 + Silent SNP A A G TCGA-DY-A0XA-01A-11D-A152-10 TCGA-DY-A0XA-10A-01D-A152-10 g.chr20:61527957A>G c.1980T>C c.(1978-1980)agT>agC p.S660S COADREAD 20 61527959 61527959 + Missense_Mutation SNP T T C TCGA-AA-3662-01A-01D-1719-10 TCGA-AA-3662-11A-01D-1719-10 g.chr20:61527959T>C c.1978A>G c.(1978-1980)Agt>Ggt p.S660G COADREAD 20 61528199 61528199 + Missense_Mutation SNP T T A TCGA-AY-6196-01A-11D-1719-10 TCGA-AY-6196-10A-01D-1719-10 g.chr20:61528199T>A c.1738A>T c.(1738-1740)Aca>Tca p.T580S COADREAD 20 61528256 61528256 + Missense_Mutation SNP G G A TCGA-A6-6781-01A-22D-1924-10 TCGA-A6-6781-10A-01D-1924-10 g.chr20:61528256G>A c.1681C>T c.(1681-1683)Cct>Tct p.P561S COADREAD 20 61537340 61537340 + Missense_Mutation SNP G G A TCGA-AA-3516-01A-02W-0833-10 TCGA-AA-3516-10A-01W-0833-10 g.chr20:61537340G>A c.1487C>T c.(1486-1488)gCa>gTa p.A496V COADREAD 20 61537402 61537402 + Frame_Shift_Del DEL T T - TCGA-A6-6653-01A-11D-1771-10 TCGA-A6-6653-10A-01D-1771-10 g.chr20:61537402delT c.1425delA c.(1423-1425)aaafs p.K475fs COADREAD 20 61537415 61537415 + Missense_Mutation SNP G G T TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr20:61537415G>T c.1412C>A c.(1411-1413)gCt>gAt p.A471D COADREAD 20 61538507 61538507 + Missense_Mutation SNP C C T TCGA-AY-6197-01A-11D-1719-10 TCGA-AY-6197-10A-01D-1719-10 g.chr20:61538507C>T c.1366G>A c.(1366-1368)Ggt>Agt p.G456S COADREAD 20 61538606 61538606 + Missense_Mutation SNP C C T TCGA-AA-A01R-01A-21W-A096-10 TCGA-AA-A01R-11A-12W-A096-10 g.chr20:61538606C>T c.1267G>A c.(1267-1269)Gca>Aca p.A423T COADREAD 20 61538626 61538626 + Missense_Mutation SNP T T C TCGA-AA-3712-01A-21D-1719-10 TCGA-AA-3712-11A-01D-1719-10 g.chr20:61538626T>C c.1247A>G c.(1246-1248)gAc>gGc p.D416G COADREAD 20 61538701 61538701 + Missense_Mutation SNP G G A TCGA-AA-3821-01A-01W-0995-10 TCGA-AA-3821-10A-01W-0995-10 g.chr20:61538701G>A c.1172C>T c.(1171-1173)gCg>gTg p.A391V COADREAD 20 61538704 61538704 + Missense_Mutation SNP T T G TCGA-AA-3877-01A-01W-0995-10 TCGA-AA-3877-10A-01W-0995-10 g.chr20:61538704T>G c.1169A>C c.(1168-1170)gAg>gCg p.E390A COADREAD 20 61542279 61542279 + Missense_Mutation SNP G G A TCGA-CM-6171-01A-11D-1650-10 TCGA-CM-6171-10A-01D-1650-10 g.chr20:61542279G>A c.686C>T c.(685-687)gCt>gTt p.A229V COADREAD 20 61542332 61542332 + Silent SNP G G A TCGA-AA-3715-01A-01W-0900-09 TCGA-AA-3715-10A-01W-0900-09 g.chr20:61542332G>A c.633C>T c.(631-633)ggC>ggT p.G211G COADREAD 20 61542512 61542512 + Silent SNP G G A TCGA-AF-2689-01A-01W-0831-10 TCGA-AF-2689-10A-01W-0831-10 g.chr20:61542512G>A c.453C>T c.(451-453)acC>acT p.T151T DLBC 20 61510849 61510849 + Silent SNP C C T TCGA-G8-6907-01A-11D-2210-10 TCGA-G8-6907-14A-01D-2210-10 g.chr20:61510849C>T c.6459G>A c.(6457-6459)agG>agA p.R2153R DLBC 20 61525488 61525488 + Silent SNP A A G TCGA-G8-6324-01A-11D-2210-10 TCGA-G8-6324-10A-01D-2210-10 g.chr20:61525488A>G c.2631T>C c.(2629-2631)tcT>tcC p.S877S DLBC 20 61526223 61526223 + Missense_Mutation SNP G G T TCGA-GS-A9TY-01A-11D-A38X-10 TCGA-GS-A9TY-10A-01D-A38X-10 g.chr20:61526223G>T c.2375C>A c.(2374-2376)aCg>aAg p.T792K DLBC 20 61528044 61528044 + Silent SNP G G A TCGA-GR-7353-01A-11D-2210-10 TCGA-GR-7353-10A-01D-2210-10 g.chr20:61528044G>A c.1893C>T c.(1891-1893)tcC>tcT p.S631S ESCA 20 61510742 61510742 + Missense_Mutation SNP C C T TCGA-IG-A3Y9-01A-12D-A247-09 TCGA-IG-A3Y9-10A-01D-A247-09 g.chr20:61510742C>T c.6566G>A c.(6565-6567)cGg>cAg p.R2189Q ESCA 20 61510960 61510961 + Frame_Shift_Del DEL CT CT - TCGA-ZR-A9CJ-01B-11D-A387-09 TCGA-ZR-A9CJ-10A-01D-A38A-09 g.chr20:61510960_61510961delCT c.6347_6348delAG c.(6346-6348)gagfs p.E2116fs ESCA 20 61511340 61511340 + Missense_Mutation SNP C C A TCGA-V5-AASW-01A-11D-A403-09 TCGA-V5-AASW-10A-01D-A403-09 g.chr20:61511340C>A c.5968G>T c.(5968-5970)Ggt>Tgt p.G1990C ESCA 20 61511438 61511438 + Missense_Mutation SNP G G A TCGA-L5-A8NF-01A-11D-A37C-09 TCGA-L5-A8NF-11A-11D-A37F-09 g.chr20:61511438G>A c.5870C>T c.(5869-5871)cCa>cTa p.P1957L ESCA 20 61511724 61511724 + Missense_Mutation SNP C C T TCGA-L5-A891-01A-11D-A36J-09 TCGA-L5-A891-11A-21D-A36M-09 g.chr20:61511724C>T c.5584G>A c.(5584-5586)Gag>Aag p.E1862K ESCA 20 61513083 61513083 + Missense_Mutation SNP C C T TCGA-L5-A8NK-01A-21D-A37C-09 TCGA-L5-A8NK-11A-11D-A37F-09 g.chr20:61513083C>T c.4225G>A c.(4225-4227)Gag>Aag p.E1409K ESCA 20 61513659 61513659 + Nonsense_Mutation SNP G G A TCGA-LN-A9FQ-01A-31D-A387-09 TCGA-LN-A9FQ-10A-01D-A38A-09 g.chr20:61513659G>A c.3649C>T c.(3649-3651)Cga>Tga p.R1217* ESCA 20 61513761 61513761 + Missense_Mutation SNP C C G TCGA-LN-A7HY-01A-12D-A351-09 TCGA-LN-A7HY-10A-01D-A351-09 g.chr20:61513761C>G c.3547G>C c.(3547-3549)Gag>Cag p.E1183Q ESCA 20 61522367 61522367 + Silent SNP G G T TCGA-L5-A4OE-01A-11D-A27G-09 TCGA-L5-A4OE-11A-11D-A27G-09 g.chr20:61522367G>T c.3486C>A c.(3484-3486)atC>atA p.I1162I ESCA 20 61524253 61524253 + Missense_Mutation SNP T T C TCGA-L5-A43J-01A-12D-A247-09 TCGA-L5-A43J-11A-11D-A247-09 g.chr20:61524253T>C c.3163A>G c.(3163-3165)Acc>Gcc p.T1055A ESCA 20 61537402 61537402 + Frame_Shift_Del DEL T T - TCGA-IG-A97H-01A-11D-A387-09 TCGA-IG-A97H-10A-01D-A38A-09 g.chr20:61537402delT c.1425delA c.(1423-1425)aaafs p.K475fs ESCA 20 61542195 61542195 + Missense_Mutation SNP G G T TCGA-R6-A6Y0-01B-11D-A33E-09 TCGA-R6-A6Y0-10A-01D-A33H-09 g.chr20:61542195G>T c.770C>A c.(769-771)cCg>cAg p.P257Q ESCA 20 61542393 61542393 + Missense_Mutation SNP T T A TCGA-L5-A88S-01A-11D-A36J-09 TCGA-L5-A88S-11A-21D-A36M-09 g.chr20:61542393T>A c.572A>T c.(571-573)aAg>aTg p.K191M GBM 20 61511189 61511189 + Missense_Mutation SNP C C T TCGA-41-3393-01A-01D-1353-08 TCGA-41-3393-10A-01D-1353-08 g.chr20:61511189C>T c.6119G>A c.(6118-6120)cGc>cAc p.R2040H GBM 20 61512320 61512320 + Missense_Mutation SNP G G A TCGA-27-1836-01A-01D-1494-08 TCGA-27-1836-10A-01D-1494-08 g.chr20:61512320G>A c.4988C>T c.(4987-4989)cCg>cTg p.P1663L GBM 20 61542712 61542712 + Missense_Mutation SNP C C T TCGA-06-0877-01A-01W-0424-08 TCGA-06-0877-10A-01W-0424-08 g.chr20:61542712C>T c.253G>A c.(253-255)Ggc>Agc p.G85S GBMLGG 20 61511189 61511189 + Missense_Mutation SNP C C T TCGA-41-3393-01A-01D-1353-08 TCGA-41-3393-10A-01D-1353-08 g.chr20:61511189C>T c.6119G>A c.(6118-6120)cGc>cAc p.R2040H GBMLGG 20 61511261 61511261 + Missense_Mutation SNP G G A TCGA-S9-A7IZ-01A-11D-A34A-08 TCGA-S9-A7IZ-10A-01D-A34A-08 g.chr20:61511261G>A c.6047C>T c.(6046-6048)cCg>cTg p.P2016L GBMLGG 20 61511322 61511322 + Missense_Mutation SNP C C T TCGA-DU-A76K-01A-11D-A33T-08 TCGA-DU-A76K-10A-01D-A33W-08 g.chr20:61511322C>T c.5986G>A c.(5986-5988)Gca>Aca p.A1996T GBMLGG 20 61511961 61511961 + Missense_Mutation SNP C C T TCGA-HT-7884-01B-11D-2395-08 TCGA-HT-7884-10A-01D-2396-08 g.chr20:61511961C>T c.5347G>A c.(5347-5349)Gaa>Aaa p.E1783K GBMLGG 20 61511992 61511992 + Silent SNP C C T TCGA-HT-7884-01B-11D-2395-08 TCGA-HT-7884-10A-01D-2396-08 g.chr20:61511992C>T c.5316G>A c.(5314-5316)ccG>ccA p.P1772P GBMLGG 20 61512320 61512320 + Missense_Mutation SNP G G A TCGA-27-1836-01A-01D-1494-08 TCGA-27-1836-10A-01D-1494-08 g.chr20:61512320G>A c.4988C>T c.(4987-4989)cCg>cTg p.P1663L GBMLGG 20 61512503 61512503 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr20:61512503C>A c.4805G>T c.(4804-4806)gGc>gTc p.G1602V GBMLGG 20 61527924 61527924 + Silent SNP C C T TCGA-DB-A64R-01A-11D-A29Q-08 TCGA-DB-A64R-10A-01D-A29Q-08 g.chr20:61527924C>T c.2013G>A c.(2011-2013)cgG>cgA p.R671R GBMLGG 20 61542712 61542712 + Missense_Mutation SNP C C T TCGA-06-0877-01A-01W-0424-08 TCGA-06-0877-10A-01W-0424-08 g.chr20:61542712C>T c.253G>A c.(253-255)Ggc>Agc p.G85S HNSC 20 61510637 61510637 + Missense_Mutation SNP G G C TCGA-CN-5367-01A-01D-1434-08 TCGA-CN-5367-10A-01D-1434-08 g.chr20:61510637G>C c.6671C>G c.(6670-6672)cCg>cGg p.P2224R HNSC 20 61511034 61511034 + Missense_Mutation SNP C C G TCGA-CN-6011-01A-11D-1683-08 TCGA-CN-6011-10A-01D-1683-08 g.chr20:61511034C>G c.6274G>C c.(6274-6276)Gac>Cac p.D2092H HNSC 20 61511058 61511058 + Missense_Mutation SNP C C T TCGA-CV-A463-01A-11D-A25Y-08 TCGA-CV-A463-10A-01D-A25Y-08 g.chr20:61511058C>T c.6250G>A c.(6250-6252)Gaa>Aaa p.E2084K HNSC 20 61511065 61511065 + Missense_Mutation SNP C C G TCGA-CN-5369-01A-01D-1434-08 TCGA-CN-5369-10A-01D-1434-08 g.chr20:61511065C>G c.6243G>C c.(6241-6243)caG>caC p.Q2081H HNSC 20 61511322 61511322 + Missense_Mutation SNP C C T TCGA-KU-A6H7-01A-11D-A31L-08 TCGA-KU-A6H7-10A-01D-A31J-08 g.chr20:61511322C>T c.5986G>A c.(5986-5988)Gca>Aca p.A1996T HNSC 20 61511582 61511582 + Missense_Mutation SNP G G A TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr20:61511582G>A c.5726C>T c.(5725-5727)cCc>cTc p.P1909L HNSC 20 61511583 61511583 + Missense_Mutation SNP G G A TCGA-D6-6516-01A-11D-1870-08 TCGA-D6-6516-10A-01D-1870-08 g.chr20:61511583G>A c.5725C>T c.(5725-5727)Ccc>Tcc p.P1909S HNSC 20 61511734 61511734 + Silent SNP G G A TCGA-CV-6436-01A-11D-1683-08 TCGA-CV-6436-11A-01D-1683-08 g.chr20:61511734G>A c.5574C>T c.(5572-5574)gcC>gcT p.A1858A HNSC 20 61511825 61511825 + Missense_Mutation SNP G G A TCGA-CR-7388-01A-11D-2012-08 TCGA-CR-7388-10A-01D-2013-08 g.chr20:61511825G>A c.5483C>T c.(5482-5484)cCc>cTc p.P1828L HNSC 20 61512130 61512130 + Missense_Mutation SNP C C A TCGA-D6-A6EM-01A-21D-A31L-08 TCGA-D6-A6EM-10A-01D-A31J-08 g.chr20:61512130C>A c.5178G>T c.(5176-5178)caG>caT p.Q1726H HNSC 20 61512534 61512534 + Missense_Mutation SNP C C T TCGA-CV-5434-01A-01D-1683-08 TCGA-CV-5434-10A-01D-1870-08 g.chr20:61512534C>T c.4774G>A c.(4774-4776)Gag>Aag p.E1592K HNSC 20 61512619 61512619 + Silent SNP C C T TCGA-C9-A480-01A-12D-A24D-08 TCGA-C9-A480-10A-01D-A24F-08 g.chr20:61512619C>T c.4689G>A c.(4687-4689)gcG>gcA p.A1563A HNSC 20 61512690 61512690 + Nonsense_Mutation SNP G G A TCGA-CX-7219-01A-11D-2012-08 TCGA-CX-7219-10A-01D-2013-08 g.chr20:61512690G>A c.4618C>T c.(4618-4620)Cag>Tag p.Q1540* HNSC 20 61513014 61513014 + Missense_Mutation SNP T T C TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr20:61513014T>C c.4294A>G c.(4294-4296)Acc>Gcc p.T1432A HNSC 20 61513015 61513015 + Missense_Mutation SNP C C G TCGA-T2-A6X2-01A-12D-A34J-08 TCGA-T2-A6X2-10B-01D-A34M-08 g.chr20:61513015C>G c.4293G>C c.(4291-4293)gaG>gaC p.E1431D HNSC 20 61513443 61513446 + Frame_Shift_Del DEL CTGT CTGT - TCGA-BA-5559-01A-01D-1512-08 TCGA-BA-5559-10A-01D-1512-08 g.chr20:61513443_61513446delCTGT c.3862_3865delACAG c.(3862-3867)acagcafs p.TA1288fs HNSC 20 61513653 61513653 + Nonsense_Mutation SNP G G A TCGA-TN-A7HL-01A-11D-A34J-08 TCGA-TN-A7HL-10A-01D-A34M-08 g.chr20:61513653G>A c.3655C>T c.(3655-3657)Caa>Taa p.Q1219* HNSC 20 61513712 61513713 + Frame_Shift_Ins INS - - T TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr20:61513712_61513713insT c.3595_3596insA c.(3595-3597)atcfs p.I1199fs HNSC 20 61525058 61525058 + Missense_Mutation SNP C C T TCGA-CR-6481-01A-11D-1870-08 TCGA-CR-6481-10A-01D-1870-08 g.chr20:61525058C>T c.3061G>A c.(3061-3063)Gac>Aac p.D1021N HNSC 20 61525097 61525097 + Missense_Mutation SNP C C A TCGA-CR-7402-01A-11D-2012-08 TCGA-CR-7402-10A-01D-2013-08 g.chr20:61525097C>A c.3022G>T c.(3022-3024)Gtg>Ttg p.V1008L HNSC 20 61525160 61525160 + Missense_Mutation SNP C C T TCGA-CR-6481-01A-11D-1870-08 TCGA-CR-6481-10A-01D-1870-08 g.chr20:61525160C>T c.2959G>A c.(2959-2961)Gac>Aac p.D987N HNSC 20 61525511 61525511 + Missense_Mutation SNP T T C TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr20:61525511T>C c.2608A>G c.(2608-2610)Aaa>Gaa p.K870E HNSC 20 61526189 61526189 + Silent SNP C C T TCGA-QK-A6VB-01A-12D-A34J-08 TCGA-QK-A6VB-10B-01D-A34M-08 g.chr20:61526189C>T c.2409G>A c.(2407-2409)gaG>gaA p.E803E HNSC 20 61527745 61527745 + Splice_Site SNP C C G TCGA-CV-7099-01A-41D-2012-08 TCGA-CV-7099-10A-01D-2013-08 g.chr20:61527745C>G c.e8-1 HNSC 20 61541176 61541176 + Missense_Mutation SNP C C G TCGA-CV-6936-01A-11D-1912-08 TCGA-CV-6936-10A-01D-1912-08 g.chr20:61541176C>G c.1036G>C c.(1036-1038)Gat>Cat p.D346H HNSC 20 61542307 61542307 + Missense_Mutation SNP C C T TCGA-CV-A461-01A-41D-A25Y-08 TCGA-CV-A461-10A-01D-A25Y-08 g.chr20:61542307C>T c.658G>A c.(658-660)Gag>Aag p.E220K HNSC 20 61542619 61542619 + Missense_Mutation SNP C C T TCGA-CV-6955-01A-11D-2012-08 TCGA-CV-6955-10A-01D-2013-08 g.chr20:61542619C>T c.346G>A c.(346-348)Gaa>Aaa p.E116K HNSC 20 61542690 61542690 + Missense_Mutation SNP G G C TCGA-T3-A92M-01A-31D-A391-08 TCGA-T3-A92M-10A-01D-A394-08 g.chr20:61542690G>C c.275C>G c.(274-276)tCc>tGc p.S92C HNSC 20 61542922 61542922 + Missense_Mutation SNP C C T TCGA-CX-7219-01A-11D-2012-08 TCGA-CX-7219-10A-01D-2013-08 g.chr20:61542922C>T c.43G>A c.(43-45)Gcc>Acc p.A15T KICH 20 61513562 61513562 + Missense_Mutation SNP G G C TCGA-KO-8408-01A-11D-2310-10 TCGA-KO-8408-11A-01D-2311-10 g.chr20:61513562G>C c.3746C>G c.(3745-3747)gCa>gGa p.A1249G KICH 20 61525220 61525220 + Missense_Mutation SNP C C A TCGA-KN-8427-01A-11D-2310-10 TCGA-KN-8427-11A-01D-2311-10 g.chr20:61525220C>A c.2899G>T c.(2899-2901)Gac>Tac p.D967Y KIPAN 20 61513427 61513438 + In_Frame_Del DEL GCTGCTGTTGTG GCTGCTGTTGTG - TCGA-CJ-4640-01A-02D-1386-10 TCGA-CJ-4640-11A-01D-1251-10 g.chr20:61513427_61513438delGCTGCTGTTGTG c.3870_3881delCACAACAGCAGC c.(3868-3882)gccacaacagcagcg>gcg p.1290_1294ATTAA>A KIPAN 20 61513486 61513486 + Missense_Mutation SNP T T A TCGA-A4-A7UZ-01A-12D-A34Z-10 TCGA-A4-A7UZ-10A-01D-A34Z-10 g.chr20:61513486T>A c.3822A>T c.(3820-3822)aaA>aaT p.K1274N KIPAN 20 61513562 61513562 + Missense_Mutation SNP G G C TCGA-KO-8408-01A-11D-2310-10 TCGA-KO-8408-11A-01D-2311-10 g.chr20:61513562G>C c.3746C>G c.(3745-3747)gCa>gGa p.A1249G KIPAN 20 61525220 61525220 + Missense_Mutation SNP C C A TCGA-KN-8427-01A-11D-2310-10 TCGA-KN-8427-11A-01D-2311-10 g.chr20:61525220C>A c.2899G>T c.(2899-2901)Gac>Tac p.D967Y KIPAN 20 61527636 61527636 + Silent SNP G G A TCGA-BP-4352-01A-01D-1366-10 TCGA-BP-4352-11A-01D-1366-10 g.chr20:61527636G>A c.2163C>T c.(2161-2163)taC>taT p.Y721Y KIPAN 20 61527694 61527695 + Frame_Shift_Ins INS - - T TCGA-GL-A9DD-01A-11D-A36X-10 TCGA-GL-A9DD-10A-01D-A370-10 g.chr20:61527694_61527695insT c.2104_2105insA c.(2104-2106)attfs p.I702fs KIPAN 20 61528138 61528138 + Missense_Mutation SNP A A T TCGA-2Z-A9JK-01A-11D-A42J-10 TCGA-2Z-A9JK-10A-01D-A42M-10 g.chr20:61528138A>T c.1799T>A c.(1798-1800)cTc>cAc p.L600H KIPAN 20 61537212 61537212 + Intron SNP G G A TCGA-CJ-4635-01A-02D-1373-10 TCGA-CJ-4635-11B-01D-1373-10 g.chr20:61537212G>A KIRC 20 61513427 61513438 + In_Frame_Del DEL GCTGCTGTTGTG GCTGCTGTTGTG - TCGA-CJ-4640-01A-02D-1386-10 TCGA-CJ-4640-11A-01D-1251-10 g.chr20:61513427_61513438delGCTGCTGTTGTG c.3870_3881delCACAACAGCAGC c.(3868-3882)gccacaacagcagcg>gcg p.1290_1294ATTAA>A KIRC 20 61527636 61527636 + Silent SNP G G A TCGA-BP-4352-01A-01D-1366-10 TCGA-BP-4352-11A-01D-1366-10 g.chr20:61527636G>A c.2163C>T c.(2161-2163)taC>taT p.Y721Y KIRC 20 61537212 61537212 + Intron SNP G G A TCGA-CJ-4635-01A-02D-1373-10 TCGA-CJ-4635-11B-01D-1373-10 g.chr20:61537212G>A KIRP 20 61513486 61513486 + Missense_Mutation SNP T T A TCGA-A4-A7UZ-01A-12D-A34Z-10 TCGA-A4-A7UZ-10A-01D-A34Z-10 g.chr20:61513486T>A c.3822A>T c.(3820-3822)aaA>aaT p.K1274N KIRP 20 61527694 61527695 + Frame_Shift_Ins INS - - T TCGA-GL-A9DD-01A-11D-A36X-10 TCGA-GL-A9DD-10A-01D-A370-10 g.chr20:61527694_61527695insT c.2104_2105insA c.(2104-2106)attfs p.I702fs KIRP 20 61528138 61528138 + Missense_Mutation SNP A A T TCGA-2Z-A9JK-01A-11D-A42J-10 TCGA-2Z-A9JK-10A-01D-A42M-10 g.chr20:61528138A>T c.1799T>A c.(1798-1800)cTc>cAc p.L600H LGG 20 61511261 61511261 + Missense_Mutation SNP G G A TCGA-S9-A7IZ-01A-11D-A34A-08 TCGA-S9-A7IZ-10A-01D-A34A-08 g.chr20:61511261G>A c.6047C>T c.(6046-6048)cCg>cTg p.P2016L LGG 20 61511322 61511322 + Missense_Mutation SNP C C T TCGA-DU-A76K-01A-11D-A33T-08 TCGA-DU-A76K-10A-01D-A33W-08 g.chr20:61511322C>T c.5986G>A c.(5986-5988)Gca>Aca p.A1996T LGG 20 61511961 61511961 + Missense_Mutation SNP C C T TCGA-HT-7884-01B-11D-2395-08 TCGA-HT-7884-10A-01D-2396-08 g.chr20:61511961C>T c.5347G>A c.(5347-5349)Gaa>Aaa p.E1783K LGG 20 61511992 61511992 + Silent SNP C C T TCGA-HT-7884-01B-11D-2395-08 TCGA-HT-7884-10A-01D-2396-08 g.chr20:61511992C>T c.5316G>A c.(5314-5316)ccG>ccA p.P1772P LGG 20 61512503 61512503 + Missense_Mutation SNP C C A TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr20:61512503C>A c.4805G>T c.(4804-4806)gGc>gTc p.G1602V LGG 20 61527924 61527924 + Silent SNP C C T TCGA-DB-A64R-01A-11D-A29Q-08 TCGA-DB-A64R-10A-01D-A29Q-08 g.chr20:61527924C>T c.2013G>A c.(2011-2013)cgG>cgA p.R671R LIHC 20 61510865 61510865 + Missense_Mutation SNP T T C TCGA-2Y-A9GS-01A-12D-A382-10 TCGA-2Y-A9GS-10A-01D-A385-10 g.chr20:61510865T>C c.6443A>G c.(6442-6444)gAc>gGc p.D2148G LIHC 20 61511261 61511261 + Missense_Mutation SNP G G T TCGA-ES-A2HS-01A-11D-A183-10 TCGA-ES-A2HS-11A-11D-A183-10 g.chr20:61511261G>T c.6047C>A c.(6046-6048)cCg>cAg p.P2016Q LIHC 20 61511712 61511712 + Missense_Mutation SNP C C T TCGA-FV-A3R3-01A-11D-A22F-10 TCGA-FV-A3R3-10A-01D-A22F-10 g.chr20:61511712C>T c.5596G>A c.(5596-5598)Gcc>Acc p.A1866T LIHC 20 61511821 61511821 + Silent SNP A A G TCGA-ED-A4XI-01A-11D-A25V-10 TCGA-ED-A4XI-10A-01D-A25V-10 g.chr20:61511821A>G c.5487T>C c.(5485-5487)tcT>tcC p.S1829S LIHC 20 61512777 61512777 + Missense_Mutation SNP T T C TCGA-CC-A7IK-01A-12D-A33Q-10 TCGA-CC-A7IK-10A-01D-A33Q-10 g.chr20:61512777T>C c.4531A>G c.(4531-4533)Atg>Gtg p.M1511V LIHC 20 61513462 61513462 + Silent SNP T T C TCGA-DD-A39Y-01A-11D-A20W-10 TCGA-DD-A39Y-11A-11D-A20W-10 g.chr20:61513462T>C c.3846A>G c.(3844-3846)gcA>gcG p.A1282A LIHC 20 61522428 61522428 + Missense_Mutation SNP C C T TCGA-CC-A7IJ-01A-11D-A33Q-10 TCGA-CC-A7IJ-10A-01D-A33Q-10 g.chr20:61522428C>T c.3425G>A c.(3424-3426)aGc>aAc p.S1142N LIHC 20 61525146 61525146 + Missense_Mutation SNP C C T TCGA-LG-A9QD-01A-11D-A382-10 TCGA-LG-A9QD-10A-01D-A385-10 g.chr20:61525146C>T c.2973G>A c.(2971-2973)atG>atA p.M991I LIHC 20 61525548 61525548 + Splice_Site SNP T T A TCGA-G3-A6UC-01A-21D-A33K-10 TCGA-G3-A6UC-10A-01D-A33K-10 g.chr20:61525548T>A c.e12-2 LIHC 20 61526440 61526440 + Silent SNP A A G TCGA-DD-AAE7-01A-11D-A40R-10 TCGA-DD-AAE7-10A-01D-A40U-10 g.chr20:61526440A>G c.2292T>C c.(2290-2292)tcT>tcC p.S764S LIHC 20 61527589 61527589 + Missense_Mutation SNP T T A TCGA-4R-AA8I-01A-11D-A382-10 TCGA-4R-AA8I-10B-01D-A385-10 g.chr20:61527589T>A c.2210A>T c.(2209-2211)aAt>aTt p.N737I LIHC 20 61528235 61528235 + Missense_Mutation SNP G G A TCGA-DD-AACD-01A-11D-A40R-10 TCGA-DD-AACD-10A-01D-A40U-10 g.chr20:61528235G>A c.1702C>T c.(1702-1704)Cca>Tca p.P568S LIHC 20 61528282 61528282 + Missense_Mutation SNP G G A TCGA-BC-A216-01A-11D-A152-10 TCGA-BC-A216-11A-11D-A152-10 g.chr20:61528282G>A c.1655C>T c.(1654-1656)cCt>cTt p.P552L LIHC 20 61537425 61537425 + Nonsense_Mutation SNP T T A TCGA-DD-AAC8-01A-11D-A40R-10 TCGA-DD-AAC8-10A-01D-A40U-10 g.chr20:61537425T>A c.1402A>T c.(1402-1404)Aag>Tag p.K468* LIHC 20 61542449 61542449 + Silent SNP C C A TCGA-DD-AAD1-01A-11D-A40R-10 TCGA-DD-AAD1-10A-01D-A40U-10 g.chr20:61542449C>A c.516G>T c.(514-516)cgG>cgT p.R172R LUAD 20 61510873 61510873 + Silent SNP C C A TCGA-95-7567-01A-11D-2063-08 TCGA-95-7567-10A-01D-2063-08 g.chr20:61510873C>A c.6435G>T c.(6433-6435)cgG>cgT p.R2145R LUAD 20 61510928 61510928 + Missense_Mutation SNP C C G TCGA-78-8662-01A-11D-2393-08 TCGA-78-8662-10A-01D-2393-08 g.chr20:61510928C>G c.6380G>C c.(6379-6381)cGg>cCg p.R2127P LUAD 20 61510951 61510951 + Silent SNP G G A TCGA-86-8672-01A-21D-2393-08 TCGA-86-8672-10A-01D-2393-08 g.chr20:61510951G>A c.6357C>T c.(6355-6357)cgC>cgT p.R2119R LUAD 20 61511128 61511128 + Missense_Mutation SNP C C A TCGA-86-8585-01A-11D-2393-08 TCGA-86-8585-10A-01D-2393-08 g.chr20:61511128C>A c.6180G>T c.(6178-6180)gaG>gaT p.E2060D LUAD 20 61511164 61511164 + Silent SNP G G A TCGA-53-7813-01A-11D-2167-08 TCGA-53-7813-10A-01D-2167-08 g.chr20:61511164G>A c.6144C>T c.(6142-6144)tcC>tcT p.S2048S LUAD 20 61511227 61511227 + Silent SNP C C A TCGA-78-8662-01A-11D-2393-08 TCGA-78-8662-10A-01D-2393-08 g.chr20:61511227C>A c.6081G>T c.(6079-6081)ctG>ctT p.L2027L LUAD 20 61511301 61511301 + Missense_Mutation SNP C C T TCGA-55-A48X-01A-11D-A24D-08 TCGA-55-A48X-10A-01D-A24F-08 g.chr20:61511301C>T c.6007G>A c.(6007-6009)Gag>Aag p.E2003K LUAD 20 61511318 61511318 + Missense_Mutation SNP G G T TCGA-44-2656-01A-02D-0969-08 TCGA-44-2656-11A-01D-1553-08 g.chr20:61511318G>T c.5990C>A c.(5989-5991)cCc>cAc p.P1997H LUAD 20 61511339 61511339 + Missense_Mutation SNP C C T TCGA-75-5146-01A-01D-1625-08 TCGA-75-5146-10A-01D-1625-08 g.chr20:61511339C>T c.5969G>A c.(5968-5970)gGt>gAt p.G1990D LUAD 20 61511468 61511468 + Missense_Mutation SNP C C A TCGA-55-8092-01A-11D-2238-08 TCGA-55-8092-10A-01D-2238-08 g.chr20:61511468C>A c.5840G>T c.(5839-5841)gGa>gTa p.G1947V LUAD 20 61511551 61511551 + Silent SNP G G T TCGA-99-8032-01A-11D-2238-08 TCGA-99-8032-10A-01D-2238-08 g.chr20:61511551G>T c.5757C>A c.(5755-5757)ccC>ccA p.P1919P LUAD 20 61511598 61511598 + Missense_Mutation SNP G G C TCGA-99-8032-01A-11D-2238-08 TCGA-99-8032-10A-01D-2238-08 g.chr20:61511598G>C c.5710C>G c.(5710-5712)Cga>Gga p.R1904G LUAD 20 61511721 61511721 + Missense_Mutation SNP C C A TCGA-69-7979-01A-11D-2184-08 TCGA-69-7979-10A-01D-2184-08 g.chr20:61511721C>A c.5587G>T c.(5587-5589)Gtg>Ttg p.V1863L LUAD 20 61511822 61511822 + Missense_Mutation SNP G G A TCGA-86-A4JF-01A-11D-A24P-08 TCGA-86-A4JF-10A-01D-A24P-08 g.chr20:61511822G>A c.5486C>T c.(5485-5487)tCt>tTt p.S1829F LUAD 20 61511984 61511984 + Missense_Mutation SNP C C G TCGA-05-4397-01A-01D-1265-08 TCGA-05-4397-10A-01D-1265-08 g.chr20:61511984C>G c.5324G>C c.(5323-5325)aGg>aCg p.R1775T LUAD 20 61512066 61512066 + Missense_Mutation SNP G G T TCGA-80-5608-01A-31D-1945-08 TCGA-80-5608-10A-01D-1946-08 g.chr20:61512066G>T c.5242C>A c.(5242-5244)Ccc>Acc p.P1748T LUAD 20 61512150 61512150 + Missense_Mutation SNP C C T TCGA-95-7944-01A-11D-2184-08 TCGA-95-7944-10A-01D-2184-08 g.chr20:61512150C>T c.5158G>A c.(5158-5160)Gag>Aag p.E1720K LUAD 20 61512238 61512238 + Silent SNP C C A TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chr20:61512238C>A c.5070G>T c.(5068-5070)tcG>tcT p.S1690S LUAD 20 61512250 61512250 + Silent SNP C C T TCGA-55-A490-01A-11D-A24D-08 TCGA-55-A490-10A-01D-A24F-08 g.chr20:61512250C>T c.5058G>A c.(5056-5058)ccG>ccA p.P1686P LUAD 20 61512318 61512318 + Missense_Mutation SNP G G A TCGA-38-4631-01A-01D-1753-08 TCGA-38-4631-11A-01D-1753-08 g.chr20:61512318G>A c.4990C>T c.(4990-4992)Cct>Tct p.P1664S LUAD 20 61512557 61512557 + Missense_Mutation SNP C C T TCGA-55-6972-01A-11D-1945-08 TCGA-55-6972-11A-01D-1945-08 g.chr20:61512557C>T c.4751G>A c.(4750-4752)cGt>cAt p.R1584H LUAD 20 61512609 61512609 + Missense_Mutation SNP C C G TCGA-95-7043-01A-11D-1945-08 TCGA-95-7043-10A-01D-1946-08 g.chr20:61512609C>G c.4699G>C c.(4699-4701)Gcc>Ccc p.A1567P LUAD 20 61512635 61512635 + Missense_Mutation SNP C C A TCGA-86-8358-01A-11D-2323-08 TCGA-86-8358-10A-01D-2323-08 g.chr20:61512635C>A c.4673G>T c.(4672-4674)aGg>aTg p.R1558M LUAD 20 61513077 61513077 + Missense_Mutation SNP C C G TCGA-49-4514-01A-21D-1855-08 TCGA-49-4514-11A-01D-1855-08 g.chr20:61513077C>G c.4231G>C c.(4231-4233)Gaa>Caa p.E1411Q LUAD 20 61513083 61513083 + Missense_Mutation SNP C C T TCGA-93-7348-01A-21D-2036-08 TCGA-93-7348-10A-01D-2036-08 g.chr20:61513083C>T c.4225G>A c.(4225-4227)Gag>Aag p.E1409K LUAD 20 61513083 61513083 + Missense_Mutation SNP C C T TCGA-MP-A4TI-01A-21D-A24P-08 TCGA-MP-A4TI-10A-01D-A24P-08 g.chr20:61513083C>T c.4225G>A c.(4225-4227)Gag>Aag p.E1409K LUAD 20 61513083 61513083 + Nonsense_Mutation SNP C C A TCGA-05-4424-01A-22D-1855-08 TCGA-05-4424-10A-01D-1855-08 g.chr20:61513083C>A c.4225G>T c.(4225-4227)Gag>Tag p.E1409* LUAD 20 61513141 61513141 + Silent SNP C C T TCGA-69-8255-01A-11D-2284-08 TCGA-69-8255-10A-01D-2284-08 g.chr20:61513141C>T c.4167G>A c.(4165-4167)gaG>gaA p.E1389E LUAD 20 61513176 61513176 + Missense_Mutation SNP C C T TCGA-17-Z057-01A-01W-0747-08 TCGA-17-Z057-11A-01W-0747-08 g.chr20:61513176C>T c.4132G>A c.(4132-4134)Gaa>Aaa p.E1378K LUAD 20 61513243 61513243 + Silent SNP C C A TCGA-97-7554-01A-11D-2036-08 TCGA-97-7554-10A-01D-2036-08 g.chr20:61513243C>A c.4065G>T c.(4063-4065)ccG>ccT p.P1355P LUAD 20 61513366 61513366 + Silent SNP C C A TCGA-17-Z017-01A-01W-0746-08 TCGA-17-Z017-11A-01W-0746-08 g.chr20:61513366C>A c.3942G>T c.(3940-3942)ctG>ctT p.L1314L LUAD 20 61513452 61513452 + Missense_Mutation SNP G G A TCGA-44-7667-01A-31D-2063-08 TCGA-44-7667-10A-01D-2063-08 g.chr20:61513452G>A c.3856C>T c.(3856-3858)Cca>Tca p.P1286S LUAD 20 61513536 61513536 + Missense_Mutation SNP G G C TCGA-83-5908-01A-21D-2284-08 TCGA-83-5908-10A-01D-2284-08 g.chr20:61513536G>C c.3772C>G c.(3772-3774)Cct>Gct p.P1258A LUAD 20 61513664 61513664 + Missense_Mutation SNP C C A TCGA-86-8673-01A-11D-2393-08 TCGA-86-8673-10A-01D-2393-08 g.chr20:61513664C>A c.3644G>T c.(3643-3645)cGg>cTg p.R1215L LUAD 20 61525342 61525342 + Missense_Mutation SNP C C T TCGA-MN-A4N4-01A-12D-A24P-08 TCGA-MN-A4N4-10A-01D-A24P-08 g.chr20:61525342C>T c.2777G>A c.(2776-2778)aGa>aAa p.R926K LUAD 20 61526418 61526418 + Missense_Mutation SNP C C G TCGA-55-8092-01A-11D-2238-08 TCGA-55-8092-10A-01D-2238-08 g.chr20:61526418C>G c.2314G>C c.(2314-2316)Gag>Cag p.E772Q LUAD 20 61528088 61528088 + Frame_Shift_Del DEL C C - TCGA-NJ-A4YF-01A-12D-A25L-08 TCGA-NJ-A4YF-10A-01D-A25L-08 g.chr20:61528088delC c.1849delG c.(1849-1851)gcafs p.A617fs LUAD 20 61528110 61528110 + Silent SNP T T A TCGA-17-Z042-01A-01W-0746-08 TCGA-17-Z042-11A-01W-0746-08 g.chr20:61528110T>A c.1827A>T c.(1825-1827)tcA>tcT p.S609S LUAD 20 61528277 61528277 + Missense_Mutation SNP C C A TCGA-44-6774-01A-21D-1855-08 TCGA-44-6774-10A-01D-1855-08 g.chr20:61528277C>A c.1660G>T c.(1660-1662)Ggc>Tgc p.G554C LUAD 20 61528308 61528308 + Silent SNP G G A TCGA-55-8208-01A-11D-2238-08 TCGA-55-8208-10A-01D-2238-08 g.chr20:61528308G>A c.1629C>T c.(1627-1629)gcC>gcT p.A543A LUAD 20 61528310 61528310 + Missense_Mutation SNP C C A TCGA-55-8208-01A-11D-2238-08 TCGA-55-8208-10A-01D-2238-08 g.chr20:61528310C>A c.1627G>T c.(1627-1629)Gcc>Tcc p.A543S LUAD 20 61528345 61528345 + Missense_Mutation SNP G G A TCGA-95-7947-01A-11D-2184-08 TCGA-95-7947-10A-01D-2184-08 g.chr20:61528345G>A c.1592C>T c.(1591-1593)aCg>aTg p.T531M LUAD 20 61537159 61537159 + Intron SNP C C T TCGA-05-4410-01A-21D-1855-08 TCGA-05-4410-10A-01D-1855-08 g.chr20:61537159C>T LUAD 20 61537321 61537321 + Silent SNP C C A TCGA-86-8585-01A-11D-2393-08 TCGA-86-8585-10A-01D-2393-08 g.chr20:61537321C>A c.1506G>T c.(1504-1506)acG>acT p.T502T LUAD 20 61537323 61537323 + Missense_Mutation SNP T T C TCGA-91-8497-01A-11D-2393-08 TCGA-91-8497-10A-01D-2393-08 g.chr20:61537323T>C c.1504A>G c.(1504-1506)Acg>Gcg p.T502A LUAD 20 61537357 61537357 + Missense_Mutation SNP T T A TCGA-55-8203-01A-11D-2238-08 TCGA-55-8203-10A-01D-2238-08 g.chr20:61537357T>A c.1470A>T c.(1468-1470)gaA>gaT p.E490D LUAD 20 61538498 61538498 + Splice_Site SNP C C A TCGA-MN-A4N4-01A-12D-A24P-08 TCGA-MN-A4N4-10A-01D-A24P-08 g.chr20:61538498C>A c.e5+1 LUAD 20 61541330 61541330 + Silent SNP G G A TCGA-44-6779-01A-11D-1855-08 TCGA-44-6779-10A-01D-1855-08 g.chr20:61541330G>A c.882C>T c.(880-882)ggC>ggT p.G294G LUAD 20 61542314 61542314 + Missense_Mutation SNP C C A TCGA-17-Z015-01A-01W-0746-08 TCGA-17-Z015-11A-01W-0746-08 g.chr20:61542314C>A c.651G>T c.(649-651)caG>caT p.Q217H LUAD 20 61542466 61542466 + Missense_Mutation SNP G G A TCGA-NJ-A4YQ-01A-11D-A25L-08 TCGA-NJ-A4YQ-10A-01D-A25L-08 g.chr20:61542466G>A c.499C>T c.(499-501)Cgc>Tgc p.R167C LUAD 20 61542492 61542492 + Missense_Mutation SNP C C A TCGA-35-5375-01A-01D-1625-08 TCGA-35-5375-10A-01D-1625-08 g.chr20:61542492C>A c.473G>T c.(472-474)gGc>gTc p.G158V LUAD 20 61542639 61542639 + Missense_Mutation SNP G G A TCGA-78-7220-01A-11D-2036-08 TCGA-78-7220-10A-01D-2036-08 g.chr20:61542639G>A c.326C>T c.(325-327)aCa>aTa p.T109I LUAD 20 61542643 61542643 + Nonsense_Mutation SNP C C A TCGA-05-4418-01A-01D-1265-08 TCGA-05-4418-10A-01D-1265-08 g.chr20:61542643C>A c.322G>T c.(322-324)Gag>Tag p.E108* LUAD 20 61542655 61542655 + Missense_Mutation SNP C C A TCGA-44-5644-01A-21D-2036-08 TCGA-44-5644-10A-01D-2036-08 g.chr20:61542655C>A c.310G>T c.(310-312)Gcc>Tcc p.A104S LUAD 20 61542656 61542656 + Silent SNP G G A TCGA-44-5644-01A-21D-2036-08 TCGA-44-5644-10A-01D-2036-08 g.chr20:61542656G>A c.309C>T c.(307-309)ccC>ccT p.P103P LUAD 20 61542745 61542745 + Missense_Mutation SNP C C A TCGA-78-7536-01A-11D-2063-08 TCGA-78-7536-10A-01D-2063-08 g.chr20:61542745C>A c.220G>T c.(220-222)Gtg>Ttg p.V74L LUAD 20 61542867 61542867 + Missense_Mutation SNP G G A TCGA-05-4432-01A-01D-1265-08 TCGA-05-4432-10A-01D-1265-08 g.chr20:61542867G>A c.98C>T c.(97-99)aCt>aTt p.T33I LUSC 20 61511697 61511697 + Missense_Mutation SNP C C T TCGA-85-6561-01A-11D-1817-08 TCGA-85-6561-10A-01D-1817-08 g.chr20:61511697C>T c.5611G>A c.(5611-5613)Gaa>Aaa p.E1871K LUSC 20 61511762 61511762 + Missense_Mutation SNP T T A TCGA-66-2727-01A-01D-0983-08 TCGA-66-2727-11A-01D-0983-08 g.chr20:61511762T>A c.5546A>T c.(5545-5547)cAt>cTt p.H1849L LUSC 20 61512009 61512009 + Missense_Mutation SNP G G A TCGA-66-2773-01A-01D-1267-08 TCGA-66-2773-11A-01D-1267-08 g.chr20:61512009G>A c.5299C>T c.(5299-5301)Cac>Tac p.H1767Y LUSC 20 61512017 61512017 + Nonsense_Mutation SNP G G T TCGA-66-2773-01A-01D-1267-08 TCGA-66-2773-11A-01D-1267-08 g.chr20:61512017G>T c.5291C>A c.(5290-5292)tCa>tAa p.S1764* LUSC 20 61512069 61512069 + Missense_Mutation SNP G G C TCGA-66-2773-01A-01D-1267-08 TCGA-66-2773-11A-01D-1267-08 g.chr20:61512069G>C c.5239C>G c.(5239-5241)Cag>Gag p.Q1747E LUSC 20 61512601 61512601 + Silent SNP C C T TCGA-66-2765-01A-01D-1522-08 TCGA-66-2765-11A-01D-1522-08 g.chr20:61512601C>T c.4707G>A c.(4705-4707)gaG>gaA p.E1569E LUSC 20 61512756 61512756 + Missense_Mutation SNP C C T TCGA-66-2785-01A-01D-1522-08 TCGA-66-2785-11A-01D-1522-08 g.chr20:61512756C>T c.4552G>A c.(4552-4554)Gac>Aac p.D1518N LUSC 20 61512895 61512896 + Missense_Mutation DNP GG GG AA TCGA-66-2773-01A-01D-1267-08 TCGA-66-2773-11A-01D-1267-08 g.chr20:61512895_61512896GG>AA c.4412_4413CC>TT c.(4411-4413)tCC>tTT p.S1471F LUSC 20 61513191 61513191 + Missense_Mutation SNP C C A TCGA-33-4586-01A-01D-1441-08 TCGA-33-4586-11A-01D-1441-08 g.chr20:61513191C>A c.4117G>T c.(4117-4119)Gat>Tat p.D1373Y LUSC 20 61513663 61513663 + Silent SNP C C T TCGA-70-6722-01A-11D-1817-08 TCGA-70-6722-10A-01D-1817-08 g.chr20:61513663C>T c.3645G>A c.(3643-3645)cgG>cgA p.R1215R LUSC 20 61522319 61522319 + Missense_Mutation SNP C C A TCGA-33-4566-01A-01D-1441-08 TCGA-33-4566-11A-01D-1441-08 g.chr20:61522319C>A c.3534G>T c.(3532-3534)gaG>gaT p.E1178D LUSC 20 61522414 61522414 + Missense_Mutation SNP C C A TCGA-66-2767-01A-01D-1522-08 TCGA-66-2767-11A-01D-1522-08 g.chr20:61522414C>A c.3439G>T c.(3439-3441)Ggt>Tgt p.G1147C LUSC 20 61525358 61525358 + Missense_Mutation SNP G G A TCGA-60-2698-01A-01D-1522-08 TCGA-60-2698-11A-01D-1522-08 g.chr20:61525358G>A c.2761C>T c.(2761-2763)Cat>Tat p.H921Y LUSC 20 61525406 61525406 + Missense_Mutation SNP C C T TCGA-18-3414-01A-01D-0983-08 TCGA-18-3414-11A-01D-0983-08 g.chr20:61525406C>T c.2713G>A c.(2713-2715)Gag>Aag p.E905K LUSC 20 61525489 61525489 + Missense_Mutation SNP G G A TCGA-22-4599-01A-01D-1441-08 TCGA-22-4599-11A-01D-1441-08 g.chr20:61525489G>A c.2630C>T c.(2629-2631)tCt>tTt p.S877F LUSC 20 61525784 61525784 + Silent SNP G G A TCGA-22-4613-01A-01D-1441-08 TCGA-22-4613-11A-01D-1441-08 g.chr20:61525784G>A c.2553C>T c.(2551-2553)ctC>ctT p.L851L LUSC 20 61527695 61527695 + Missense_Mutation SNP T T C TCGA-85-6560-01A-11D-1817-08 TCGA-85-6560-10A-01D-1817-08 g.chr20:61527695T>C c.2104A>G c.(2104-2106)Att>Gtt p.I702V LUSC 20 61528077 61528077 + Silent SNP C C A TCGA-70-6722-01A-11D-1817-08 TCGA-70-6722-10A-01D-1817-08 g.chr20:61528077C>A c.1860G>T c.(1858-1860)gcG>gcT p.A620A LUSC 20 61528146 61528146 + Silent SNP C C T TCGA-66-2759-01A-01D-1522-08 TCGA-66-2759-11A-01D-1522-08 g.chr20:61528146C>T c.1791G>A c.(1789-1791)agG>agA p.R597R LUSC 20 61537362 61537362 + Missense_Mutation SNP T T C TCGA-39-5036-01A-01D-1441-08 TCGA-39-5036-11A-01D-1441-08 g.chr20:61537362T>C c.1465A>G c.(1465-1467)Agt>Ggt p.S489G LUSC 20 61541126 61541126 + Missense_Mutation SNP T T G TCGA-46-3767-01A-01D-0983-08 TCGA-46-3767-10A-01D-0983-08 g.chr20:61541126T>G c.1086A>C c.(1084-1086)gaA>gaC p.E362D OV 20 61512109 61512109 + Silent SNP G G A TCGA-59-2372-01A-01D-1526-09 TCGA-59-2372-10A-01D-1526-09 g.chr20:61512109G>A c.5199C>T c.(5197-5199)acC>acT p.T1733T OV 20 61527958 61527958 + Missense_Mutation SNP C C T TCGA-13-0924-01A-01W-0421-09 TCGA-13-0924-10A-01W-0421-09 g.chr20:61527958C>T c.1979G>A c.(1978-1980)aGt>aAt p.S660N OV 20 61538627 61538627 + Missense_Mutation SNP C C T TCGA-24-1463-01A-01W-0549-09 TCGA-24-1463-10A-01W-0549-09 g.chr20:61538627C>T c.1246G>A c.(1246-1248)Gac>Aac p.D416N OV 20 61541214 61541214 + Missense_Mutation SNP G G A TCGA-13-1512-01A-01W-0545-08 TCGA-13-1512-10A-01W-0546-08 g.chr20:61541214G>A c.998C>T c.(997-999)gCa>gTa p.A333V OV 20 61542565 61542565 + Missense_Mutation SNP C C G TCGA-29-1770-01A-01W-0633-09 TCGA-29-1770-10A-01W-0634-09 g.chr20:61542565C>G c.400G>C c.(400-402)Gaa>Caa p.E134Q PAAD 20 61510917 61510917 + Missense_Mutation SNP G G A TCGA-RL-AAAS-01A-32D-A397-08 TCGA-RL-AAAS-10A-01D-A39A-08 g.chr20:61510917G>A c.6391C>T c.(6391-6393)Cgg>Tgg p.R2131W PAAD 20 61511164 61511164 + Silent SNP G G A TCGA-2J-AABF-01A-31D-A40W-08 TCGA-2J-AABF-10A-01D-A40W-08 g.chr20:61511164G>A c.6144C>T c.(6142-6144)tcC>tcT p.S2048S PAAD 20 61511303 61511303 + Frame_Shift_Del DEL T T - TCGA-HV-A7OP-01A-11D-A33T-08 TCGA-HV-A7OP-10A-01D-A33W-08 g.chr20:61511303delT c.6005delA c.(6004-6006)aatfs p.N2002fs PAAD 20 61511303 61511303 + Frame_Shift_Del DEL T T - TCGA-US-A77E-01A-11D-A32N-08 TCGA-US-A77E-11A-11D-A32N-08 g.chr20:61511303delT c.6005delA c.(6004-6006)aatfs p.N2002fs PAAD 20 61511322 61511322 + Missense_Mutation SNP C C T TCGA-F2-A7TX-01A-33D-A38G-08 TCGA-F2-A7TX-10B-01D-A38J-08 g.chr20:61511322C>T c.5986G>A c.(5986-5988)Gca>Aca p.A1996T PAAD 20 61511322 61511322 + Missense_Mutation SNP C C T TCGA-RL-AAAS-01A-32D-A397-08 TCGA-RL-AAAS-10A-01D-A39A-08 g.chr20:61511322C>T c.5986G>A c.(5986-5988)Gca>Aca p.A1996T PAAD 20 61511392 61511392 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr20:61511392G>A c.5916C>T c.(5914-5916)gtC>gtT p.V1972V PAAD 20 61512121 61512121 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr20:61512121G>A c.5187C>T c.(5185-5187)ccC>ccT p.P1729P PAAD 20 61512142 61512142 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr20:61512142G>A c.5166C>T c.(5164-5166)gaC>gaT p.D1722D PAAD 20 61512310 61512310 + Silent SNP G G T TCGA-3A-A9I9-01A-11D-A38G-08 TCGA-3A-A9I9-10A-01D-A38J-08 g.chr20:61512310G>T c.4998C>A c.(4996-4998)ggC>ggA p.G1666G PAAD 20 61512380 61512381 + Frame_Shift_Ins INS - - G TCGA-2L-AAQA-01A-21D-A38G-08 TCGA-2L-AAQA-11A-11D-A38J-08 g.chr20:61512380_61512381insG c.4927_4928insC c.(4927-4929)cgcfs p.R1643fs PAAD 20 61512380 61512381 + Frame_Shift_Ins INS - - G TCGA-3A-A9IJ-01A-11D-A397-08 TCGA-3A-A9IJ-10A-01D-A39A-08 g.chr20:61512380_61512381insG c.4927_4928insC c.(4927-4929)cgcfs p.R1643fs PAAD 20 61512380 61512381 + Frame_Shift_Ins INS - - G TCGA-FB-A5VM-01A-11D-A32N-08 TCGA-FB-A5VM-10A-01D-A32N-08 g.chr20:61512380_61512381insG c.4927_4928insC c.(4927-4929)cgcfs p.R1643fs PAAD 20 61512380 61512381 + Frame_Shift_Ins INS - - G TCGA-IB-8126-01A-11D-2396-08 TCGA-IB-8126-10A-01D-2396-08 g.chr20:61512380_61512381insG c.4927_4928insC c.(4927-4929)cgcfs p.R1643fs PAAD 20 61512380 61512381 + Frame_Shift_Ins INS - - G TCGA-IB-A5SS-01A-11D-A32N-08 TCGA-IB-A5SS-10A-01D-A32N-08 g.chr20:61512380_61512381insG c.4927_4928insC c.(4927-4929)cgcfs p.R1643fs PAAD 20 61512380 61512381 + Frame_Shift_Ins INS - - G TCGA-RB-AA9M-01A-11D-A397-08 TCGA-RB-AA9M-10A-01D-A39A-08 g.chr20:61512380_61512381insG c.4927_4928insC c.(4927-4929)cgcfs p.R1643fs PAAD 20 61512959 61512959 + Missense_Mutation SNP G G A TCGA-2L-AAQJ-01A-12D-A397-08 TCGA-2L-AAQJ-11A-11D-A39A-08 g.chr20:61512959G>A c.4349C>T c.(4348-4350)gCc>gTc p.A1450V PAAD 20 61513253 61513253 + Missense_Mutation SNP T T C TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr20:61513253T>C c.4055A>G c.(4054-4056)gAc>gGc p.D1352G PAAD 20 61513415 61513415 + Missense_Mutation SNP G G A TCGA-Z5-AAPL-01A-12D-A40W-08 TCGA-Z5-AAPL-10A-01D-A40W-08 g.chr20:61513415G>A c.3893C>T c.(3892-3894)aCg>aTg p.T1298M PAAD 20 61513636 61513636 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr20:61513636G>A c.3672C>T c.(3670-3672)gaC>gaT p.D1224D PAAD 20 61522306 61522306 + Intron SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr20:61522306G>A PAAD 20 61522358 61522358 + Silent SNP G G A TCGA-2L-AAQA-01A-21D-A38G-08 TCGA-2L-AAQA-11A-11D-A38J-08 g.chr20:61522358G>A c.3495C>T c.(3493-3495)agC>agT p.S1165S PAAD 20 61525063 61525063 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr20:61525063G>A c.3056C>T c.(3055-3057)tCt>tTt p.S1019F PAAD 20 61525105 61525105 + Missense_Mutation SNP G G T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr20:61525105G>T c.3014C>A c.(3013-3015)tCt>tAt p.S1005Y PAAD 20 61525110 61525110 + Silent SNP C C T TCGA-2J-AAB1-01A-11D-A40W-08 TCGA-2J-AAB1-10A-01D-A40W-08 g.chr20:61525110C>T c.3009G>A c.(3007-3009)ttG>ttA p.L1003L PAAD 20 61528081 61528081 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr20:61528081G>A c.1856C>T c.(1855-1857)gCa>gTa p.A619V PAAD 20 61537393 61537393 + Silent SNP T T C TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr20:61537393T>C c.1434A>G c.(1432-1434)acA>acG p.T478T PAAD 20 61538515 61538515 + Missense_Mutation SNP G G T TCGA-YY-A8LH-01A-11D-A36O-08 TCGA-YY-A8LH-10A-01D-A367-08 g.chr20:61538515G>T c.1358C>A c.(1357-1359)cCg>cAg p.P453Q PAAD 20 61541345 61541345 + Missense_Mutation SNP T T A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr20:61541345T>A c.867A>T c.(865-867)gaA>gaT p.E289D PAAD 20 61542332 61542332 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr20:61542332G>A c.633C>T c.(631-633)ggC>ggT p.G211G PAAD 20 61542497 61542497 + Silent SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr20:61542497G>A c.468C>T c.(466-468)agC>agT p.S156S PAAD 20 61542721 61542721 + Missense_Mutation SNP G G A TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr20:61542721G>A c.244C>T c.(244-246)Cgg>Tgg p.R82W PCPG 20 61511023 61511023 + Silent SNP G G T TCGA-WB-A81R-01A-11D-A35I-08 TCGA-WB-A81R-10A-01D-A35G-08 g.chr20:61511023G>T c.6285C>A c.(6283-6285)ccC>ccA p.P2095P PCPG 20 61512558 61512558 + Missense_Mutation SNP G G T TCGA-WB-A81J-01A-11D-A35I-08 TCGA-WB-A81J-10A-01D-A35G-08 g.chr20:61512558G>T c.4750C>A c.(4750-4752)Cgt>Agt p.R1584S PCPG 20 61542656 61542656 + Silent SNP G G C TCGA-TT-A6YK-01A-11D-A35I-08 TCGA-TT-A6YK-10A-01D-A35G-08 g.chr20:61542656G>C c.309C>G c.(307-309)ccC>ccG p.P103P PRAD 20 61510982 61510982 + Missense_Mutation SNP G G A TCGA-KK-A59V-01A-11D-A29Q-08 TCGA-KK-A59V-11A-11D-A29Q-08 g.chr20:61510982G>A c.6326C>T c.(6325-6327)gCg>gTg p.A2109V PRAD 20 61511164 61511164 + Silent SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr20:61511164G>A c.6144C>T c.(6142-6144)tcC>tcT p.S2048S PRAD 20 61512748 61512748 + Silent SNP C C T TCGA-XK-AAJ3-01A-11D-A41K-08 TCGA-XK-AAJ3-10A-01D-A41N-08 g.chr20:61512748C>T c.4560G>A c.(4558-4560)ttG>ttA p.L1520L PRAD 20 61513251 61513251 + Missense_Mutation SNP C C T TCGA-X4-A8KS-01A-12D-A364-08 TCGA-X4-A8KS-10A-01D-A362-08 g.chr20:61513251C>T c.4057G>A c.(4057-4059)Ggg>Agg p.G1353R PRAD 20 61513601 61513601 + Missense_Mutation SNP T T C TCGA-HC-A4ZV-01A-11D-A26M-08 TCGA-HC-A4ZV-10A-01D-A26K-08 g.chr20:61513601T>C c.3707A>G c.(3706-3708)cAg>cGg p.Q1236R PRAD 20 61513671 61513671 + Missense_Mutation SNP C C T TCGA-J9-A52C-01A-11D-A26M-08 TCGA-J9-A52C-10A-01D-A26K-08 g.chr20:61513671C>T c.3637G>A c.(3637-3639)Gaa>Aaa p.E1213K PRAD 20 61525227 61525227 + Silent SNP G G A TCGA-CH-5750-01A-11D-1576-08 TCGA-CH-5750-10A-01D-1576-08 g.chr20:61525227G>A c.2892C>T c.(2890-2892)tcC>tcT p.S964S PRAD 20 61525242 61525242 + Silent SNP G G A TCGA-EJ-A46G-01A-31D-A26M-08 TCGA-EJ-A46G-10A-01D-A26K-08 g.chr20:61525242G>A c.2877C>T c.(2875-2877)acC>acT p.T959T PRAD 20 61527732 61527732 + Silent SNP G G A TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr20:61527732G>A c.2067C>T c.(2065-2067)agC>agT p.S689S PRAD 20 61538606 61538606 + Missense_Mutation SNP C C T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr20:61538606C>T c.1267G>A c.(1267-1269)Gca>Aca p.A423T PRAD 20 61541166 61541166 + Missense_Mutation SNP T T C TCGA-V1-A8WL-01A-11D-A377-08 TCGA-V1-A8WL-10A-01D-A37A-08 g.chr20:61541166T>C c.1046A>G c.(1045-1047)gAt>gGt p.D349G READ 20 61511660 61511660 + Missense_Mutation SNP C C A TCGA-AG-3999-01A-01W-1073-09 TCGA-AG-3999-10A-01W-1073-09 g.chr20:61511660C>A c.5648G>T c.(5647-5649)gGc>gTc p.G1883V READ 20 61513251 61513251 + Missense_Mutation SNP C C T TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr20:61513251C>T c.4057G>A c.(4057-4059)Ggg>Agg p.G1353R READ 20 61513408 61513408 + Silent SNP A A G TCGA-CL-5918-01A-11D-1657-10 TCGA-CL-5918-10A-01D-1657-10 g.chr20:61513408A>G c.3900T>C c.(3898-3900)gcT>gcC p.A1300A READ 20 61513713 61513713 + Frame_Shift_Del DEL T T - TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr20:61513713delT c.3595delA c.(3595-3597)atcfs p.I1199fs READ 20 61524262 61524262 + Nonsense_Mutation SNP G G A TCGA-AG-A002-01A-01W-A00K-09 TCGA-AG-A002-10A-01W-A00K-09 g.chr20:61524262G>A c.3154C>T c.(3154-3156)Cga>Tga p.R1052* READ 20 61527957 61527957 + Silent SNP A A G TCGA-DY-A0XA-01A-11D-A152-10 TCGA-DY-A0XA-10A-01D-A152-10 g.chr20:61527957A>G c.1980T>C c.(1978-1980)agT>agC p.S660S READ 20 61542512 61542512 + Silent SNP G G A TCGA-AF-2689-01A-01W-0831-10 TCGA-AF-2689-10A-01W-0831-10 g.chr20:61542512G>A c.453C>T c.(451-453)acC>acT p.T151T SARC 20 61511108 61511108 + Missense_Mutation SNP G G A TCGA-QC-A7B5-01A-11D-A33E-09 TCGA-QC-A7B5-11A-11D-A33H-09 g.chr20:61511108G>A c.6200C>T c.(6199-6201)tCg>tTg p.S2067L SARC 20 61512209 61512209 + Frame_Shift_Del DEL T T - TCGA-DX-A1L1-01A-11D-A24N-09 TCGA-DX-A1L1-10A-01D-A24N-09 g.chr20:61512209delT c.5099delA c.(5098-5100)tatfs p.Y1700fs SKCM 20 61510880 61510880 + Missense_Mutation SNP G G A TCGA-QB-A6FS-06A-11D-A30X-08 TCGA-QB-A6FS-10A-01D-A30X-08 g.chr20:61510880G>A c.6428C>T c.(6427-6429)tCc>tTc p.S2143F SKCM 20 61510928 61510928 + Missense_Mutation SNP C C T TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr20:61510928C>T c.6380G>A c.(6379-6381)cGg>cAg p.R2127Q SKCM 20 61510970 61510970 + Missense_Mutation SNP C C T TCGA-EE-A3JB-06A-11D-A21A-08 TCGA-EE-A3JB-10A-01D-A21A-08 g.chr20:61510970C>T c.6338G>A c.(6337-6339)aGg>aAg p.R2113K SKCM 20 61511130 61511130 + Missense_Mutation SNP C C T TCGA-ER-A42L-06A-11D-A24R-08 TCGA-ER-A42L-10A-01D-A24R-08 g.chr20:61511130C>T c.6178G>A c.(6178-6180)Gag>Aag p.E2060K SKCM 20 61511132 61511132 + Missense_Mutation SNP G G A TCGA-EE-A183-06A-11D-A196-08 TCGA-EE-A183-10A-01D-A198-08 g.chr20:61511132G>A c.6176C>T c.(6175-6177)cCc>cTc p.P2059L SKCM 20 61511156 61511156 + Missense_Mutation SNP G G A TCGA-D3-A5GN-06A-11D-A27K-08 TCGA-D3-A5GN-10A-01D-A27N-08 g.chr20:61511156G>A c.6152C>T c.(6151-6153)tCc>tTc p.S2051F SKCM 20 61511288 61511288 + Missense_Mutation SNP G G A TCGA-FS-A1ZQ-06A-11D-A197-08 TCGA-FS-A1ZQ-10A-01D-A199-08 g.chr20:61511288G>A c.6020C>T c.(6019-6021)tCg>tTg p.S2007L SKCM 20 61511288 61511288 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr20:61511288G>A c.6020C>T c.(6019-6021)tCg>tTg p.S2007L SKCM 20 61511312 61511312 + Missense_Mutation SNP G G A TCGA-EE-A3AG-06A-31D-A196-08 TCGA-EE-A3AG-10A-01D-A198-08 g.chr20:61511312G>A c.5996C>T c.(5995-5997)tCt>tTt p.S1999F SKCM 20 61511323 61511323 + Silent SNP G G A TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr20:61511323G>A c.5985C>T c.(5983-5985)tcC>tcT p.S1995S SKCM 20 61511407 61511407 + Silent SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr20:61511407G>A c.5901C>T c.(5899-5901)ttC>ttT p.F1967F SKCM 20 61511438 61511438 + Missense_Mutation SNP G G A TCGA-EE-A2GR-06A-11D-A197-08 TCGA-EE-A2GR-10A-01D-A199-08 g.chr20:61511438G>A c.5870C>T c.(5869-5871)cCa>cTa p.P1957L SKCM 20 61511484 61511484 + Missense_Mutation SNP G G A TCGA-D3-A2JL-06A-11D-A196-08 TCGA-D3-A2JL-10A-01D-A198-08 g.chr20:61511484G>A c.5824C>T c.(5824-5826)Ccc>Tcc p.P1942S SKCM 20 61511758 61511758 + Silent SNP C C T TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr20:61511758C>T c.5550G>A c.(5548-5550)ggG>ggA p.G1850G SKCM 20 61511759 61511759 + Missense_Mutation SNP C C T TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr20:61511759C>T c.5549G>A c.(5548-5550)gGg>gAg p.G1850E SKCM 20 61511764 61511764 + Silent SNP G G A TCGA-EE-A2GC-06A-11D-A197-08 TCGA-EE-A2GC-10A-01D-A199-08 g.chr20:61511764G>A c.5544C>T c.(5542-5544)ccC>ccT p.P1848P SKCM 20 61511765 61511765 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr20:61511765G>A c.5543C>T c.(5542-5544)cCc>cTc p.P1848L SKCM 20 61511906 61511906 + Missense_Mutation SNP C C T TCGA-EE-A2MI-06A-11D-A197-08 TCGA-EE-A2MI-10A-01D-A199-08 g.chr20:61511906C>T c.5402G>A c.(5401-5403)gGa>gAa p.G1801E SKCM 20 61511949 61511949 + Missense_Mutation SNP C C T TCGA-D9-A148-06A-11D-A19A-08 TCGA-D9-A148-10A-01D-A19A-08 g.chr20:61511949C>T c.5359G>A c.(5359-5361)Gct>Act p.A1787T SKCM 20 61511969 61511969 + Missense_Mutation SNP G G A TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr20:61511969G>A c.5339C>T c.(5338-5340)cCg>cTg p.P1780L SKCM 20 61511969 61511969 + Missense_Mutation SNP G G C TCGA-DA-A1HY-06A-11D-A19A-08 TCGA-DA-A1HY-10A-01D-A19A-08 g.chr20:61511969G>C c.5339C>G c.(5338-5340)cCg>cGg p.P1780R SKCM 20 61511988 61511988 + Missense_Mutation SNP G G A TCGA-ER-A19F-06A-11D-A196-08 TCGA-ER-A19F-10A-01D-A198-08 g.chr20:61511988G>A c.5320C>T c.(5320-5322)Cca>Tca p.P1774S SKCM 20 61512000 61512000 + Missense_Mutation SNP T T C TCGA-EE-A2A0-06A-11D-A196-08 TCGA-EE-A2A0-10A-01D-A198-08 g.chr20:61512000T>C c.5308A>G c.(5308-5310)Aat>Gat p.N1770D SKCM 20 61512110 61512110 + Missense_Mutation SNP G G A TCGA-GN-A4U7-06A-21D-A32N-08 TCGA-GN-A4U7-10B-01D-A32N-08 g.chr20:61512110G>A c.5198C>T c.(5197-5199)aCc>aTc p.T1733I SKCM 20 61512276 61512276 + Missense_Mutation SNP C C T TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr20:61512276C>T c.5032G>A c.(5032-5034)Ggt>Agt p.G1678S SKCM 20 61512325 61512325 + Silent SNP G G A TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr20:61512325G>A c.4983C>T c.(4981-4983)ccC>ccT p.P1661P SKCM 20 61512356 61512356 + Missense_Mutation SNP G G A TCGA-EE-A182-06A-11D-A196-08 TCGA-EE-A182-10A-01D-A198-08 g.chr20:61512356G>A c.4952C>T c.(4951-4953)tCg>tTg p.S1651L SKCM 20 61512461 61512461 + Missense_Mutation SNP G G A TCGA-D9-A149-06A-11D-A196-08 TCGA-D9-A149-10A-01D-A198-08 g.chr20:61512461G>A c.4847C>T c.(4846-4848)tCt>tTt p.S1616F SKCM 20 61512521 61512521 + Missense_Mutation SNP G G A TCGA-EE-A20C-06A-11D-A196-08 TCGA-EE-A20C-10A-01D-A198-08 g.chr20:61512521G>A c.4787C>T c.(4786-4788)tCc>tTc p.S1596F SKCM 20 61512921 61512921 + Missense_Mutation SNP G G A TCGA-GN-A4U7-06A-21D-A32N-08 TCGA-GN-A4U7-10B-01D-A32N-08 g.chr20:61512921G>A c.4387C>T c.(4387-4389)Ccg>Tcg p.P1463S SKCM 20 61512940 61512940 + Silent SNP G G A TCGA-EE-A29S-06A-11D-A197-08 TCGA-EE-A29S-10A-01D-A199-08 g.chr20:61512940G>A c.4368C>T c.(4366-4368)tcC>tcT p.S1456S SKCM 20 61513160 61513160 + Missense_Mutation SNP C C T TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr20:61513160C>T c.4148G>A c.(4147-4149)aGg>aAg p.R1383K SKCM 20 61513219 61513219 + Silent SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr20:61513219G>A c.4089C>T c.(4087-4089)atC>atT p.I1363I SKCM 20 61513264 61513264 + Silent SNP G G A TCGA-D9-A3Z1-06A-11D-A23B-08 TCGA-D9-A3Z1-10A-01D-A23B-08 g.chr20:61513264G>A c.4044C>T c.(4042-4044)acC>acT p.T1348T SKCM 20 61513284 61513284 + Missense_Mutation SNP G G A TCGA-EE-A2MS-06A-11D-A197-08 TCGA-EE-A2MS-10A-01D-A199-08 g.chr20:61513284G>A c.4024C>T c.(4024-4026)Ctc>Ttc p.L1342F SKCM 20 61513394 61513394 + Missense_Mutation SNP G G A TCGA-EE-A29V-06A-12D-A197-08 TCGA-EE-A29V-10A-01D-A199-08 g.chr20:61513394G>A c.3914C>T c.(3913-3915)tCg>tTg p.S1305L SKCM 20 61513426 61513426 + Silent SNP C C G TCGA-ER-A19P-06A-11D-A196-08 TCGA-ER-A19P-10A-01D-A198-08 g.chr20:61513426C>G c.3882G>C c.(3880-3882)gcG>gcC p.A1294A SKCM 20 61513451 61513451 + Missense_Mutation SNP G G A TCGA-ER-A19A-06A-21D-A197-08 TCGA-ER-A19A-10A-01D-A199-08 g.chr20:61513451G>A c.3857C>T c.(3856-3858)cCa>cTa p.P1286L SKCM 20 61513506 61513506 + Missense_Mutation SNP G G A TCGA-EE-A3JA-06A-11D-A20D-08 TCGA-EE-A3JA-10A-01D-A20D-08 g.chr20:61513506G>A c.3802C>T c.(3802-3804)Cca>Tca p.P1268S SKCM 20 61513529 61513529 + Missense_Mutation SNP G G A TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr20:61513529G>A c.3779C>T c.(3778-3780)tCg>tTg p.S1260L SKCM 20 61525205 61525205 + Missense_Mutation SNP G G A TCGA-EE-A2GC-06A-11D-A197-08 TCGA-EE-A2GC-10A-01D-A199-08 g.chr20:61525205G>A c.2914C>T c.(2914-2916)Cca>Tca p.P972S SKCM 20 61525227 61525227 + Silent SNP G G A TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr20:61525227G>A c.2892C>T c.(2890-2892)tcC>tcT p.S964S SKCM 20 61525396 61525396 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr20:61525396G>A c.2723C>T c.(2722-2724)cCt>cTt p.P908L SKCM 20 61525489 61525489 + Missense_Mutation SNP G G A TCGA-EE-A29M-06A-11D-A196-08 TCGA-EE-A29M-10A-01D-A198-08 g.chr20:61525489G>A c.2630C>T c.(2629-2631)tCt>tTt p.S877F SKCM 20 61525513 61525513 + Missense_Mutation SNP G G A TCGA-D3-A2JL-06A-11D-A196-08 TCGA-D3-A2JL-10A-01D-A198-08 g.chr20:61525513G>A c.2606C>T c.(2605-2607)cCg>cTg p.P869L SKCM 20 61525514 61525514 + Missense_Mutation SNP G G A TCGA-D3-A2JL-06A-11D-A196-08 TCGA-D3-A2JL-10A-01D-A198-08 g.chr20:61525514G>A c.2605C>T c.(2605-2607)Ccg>Tcg p.P869S SKCM 20 61525538 61525538 + Missense_Mutation SNP G G A TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr20:61525538G>A c.2581C>T c.(2581-2583)Ccc>Tcc p.P861S SKCM 20 61526218 61526218 + Missense_Mutation SNP G G A TCGA-EE-A2GO-06A-11D-A196-08 TCGA-EE-A2GO-10A-01D-A198-08 g.chr20:61526218G>A c.2380C>T c.(2380-2382)Ccc>Tcc p.P794S SKCM 20 61527623 61527623 + Missense_Mutation SNP G G A TCGA-EE-A3JD-06A-11D-A20D-08 TCGA-EE-A3JD-10A-01D-A20D-08 g.chr20:61527623G>A c.2176C>T c.(2176-2178)Cgc>Tgc p.R726C SKCM 20 61528027 61528027 + Missense_Mutation SNP G G A TCGA-EE-A2MR-06A-11D-A196-08 TCGA-EE-A2MR-10A-01D-A198-08 g.chr20:61528027G>A c.1910C>T c.(1909-1911)gCc>gTc p.A637V SKCM 20 61528167 61528167 + Silent SNP G G A TCGA-ER-A19F-06A-11D-A196-08 TCGA-ER-A19F-10A-01D-A198-08 g.chr20:61528167G>A c.1770C>T c.(1768-1770)ttC>ttT p.F590F SKCM 20 61528235 61528235 + Missense_Mutation SNP G G A TCGA-DA-A1I0-06A-11D-A20D-08 TCGA-DA-A1I0-10B-01D-A20D-08 g.chr20:61528235G>A c.1702C>T c.(1702-1704)Cca>Tca p.P568S SKCM 20 61528239 61528239 + Silent SNP G G A TCGA-ER-A42L-06A-11D-A24R-08 TCGA-ER-A42L-10A-01D-A24R-08 g.chr20:61528239G>A c.1698C>T c.(1696-1698)ctC>ctT p.L566L SKCM 20 61528272 61528272 + Silent SNP G G A TCGA-ER-A3PL-06A-11D-A23B-08 TCGA-ER-A3PL-10A-01D-A23B-08 g.chr20:61528272G>A c.1665C>T c.(1663-1665)tcC>tcT p.S555S SKCM 20 61528327 61528327 + Missense_Mutation SNP G G A TCGA-EE-A2MJ-06A-11D-A197-08 TCGA-EE-A2MJ-10A-01D-A199-08 g.chr20:61528327G>A c.1610C>T c.(1609-1611)tCc>tTc p.S537F SKCM 20 61537163 61537173 + Intron DEL CCTGGACAGGC CCTGGACAGGC - TCGA-EE-A20H-06A-11D-A197-08 TCGA-EE-A20H-10A-01D-A199-08 g.chr20:61537163_61537173delCCTGGACAGGC SKCM 20 61537178 61537178 + Intron SNP G G A TCGA-FS-A1ZD-06A-11D-A197-08 TCGA-FS-A1ZD-10A-01D-A199-08 g.chr20:61537178G>A SKCM 20 61537180 61537180 + Intron SNP G G A TCGA-D3-A51T-06A-11D-A25O-08 TCGA-D3-A51T-10A-01D-A25O-08 g.chr20:61537180G>A SKCM 20 61537180 61537180 + Intron SNP G G A TCGA-EE-A17X-06A-11D-A197-08 TCGA-EE-A17X-10A-01D-A199-08 g.chr20:61537180G>A SKCM 20 61537257 61537257 + Missense_Mutation SNP G G A TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr20:61537257G>A c.1570C>T c.(1570-1572)Ccg>Tcg p.P524S SKCM 20 61537302 61537302 + Missense_Mutation SNP G G A TCGA-ER-A19A-06A-21D-A197-08 TCGA-ER-A19A-10A-01D-A199-08 g.chr20:61537302G>A c.1525C>T c.(1525-1527)Cac>Tac p.H509Y SKCM 20 61538515 61538515 + Missense_Mutation SNP G G A TCGA-D3-A2JK-06A-11D-A196-08 TCGA-D3-A2JK-10A-01D-A198-08 g.chr20:61538515G>A c.1358C>T c.(1357-1359)cCg>cTg p.P453L SKCM 20 61542308 61542308 + Silent SNP G G A TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr20:61542308G>A c.657C>T c.(655-657)ccC>ccT p.P219P SKCM 20 61542327 61542327 + Missense_Mutation SNP A A G TCGA-D9-A149-06A-11D-A196-08 TCGA-D9-A149-10A-01D-A198-08 g.chr20:61542327A>G c.638T>C c.(637-639)cTg>cCg p.L213P SKCM 20 61542375 61542375 + Missense_Mutation SNP G G A TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr20:61542375G>A c.590C>T c.(589-591)cCc>cTc p.P197L SKCM 20 61542525 61542525 + Missense_Mutation SNP T T C TCGA-ER-A19N-06A-11D-A197-08 TCGA-ER-A19N-10A-01D-A199-08 g.chr20:61542525T>C c.440A>G c.(439-441)gAc>gGc p.D147G SKCM 20 61542779 61542779 + Silent SNP C C T TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr20:61542779C>T c.186G>A c.(184-186)cgG>cgA p.R62R SKCM 20 61542780 61542780 + Missense_Mutation SNP C C T TCGA-EE-A29D-06A-11D-A197-08 TCGA-EE-A29D-10A-01D-A199-08 g.chr20:61542780C>T c.185G>A c.(184-186)cGg>cAg p.R62Q SKCM 20 61542877 61542877 + Nonsense_Mutation SNP G G A TCGA-D3-A5GO-06A-12D-A27K-08 TCGA-D3-A5GO-10A-01D-A27N-08 g.chr20:61542877G>A c.88C>T c.(88-90)Cga>Tga p.R30* SKCM 20 61542877 61542877 + Nonsense_Mutation SNP G G A TCGA-DA-A1I8-06A-11D-A197-08 TCGA-DA-A1I8-10A-01D-A199-08 g.chr20:61542877G>A c.88C>T c.(88-90)Cga>Tga p.R30*

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 20 61512838 61512838 single base substitution C G missense_variant K1490N 4470G>C BLCA-CN 20 61512957 61512957 single base substitution C G missense_variant D1451H 4351G>C BLCA-CN 20 61513499 61513499 single base substitution G A missense_variant P1270L 3809C>T BLCA-CN 20 61528130 61528130 single base substitution T G missense_variant T603P 1807A>C BLCA-US 20 61511415 61511415 single base substitution G A stop_gained Q1965* 5893C>T BLCA-US 20 61511837 61511837 single base substitution C G missense_variant R1824T 5471G>C BLCA-US 20 61511882 61511882 single base substitution G T missense_variant S1809Y 5426C>A BLCA-US 20 61512150 61512150 single base substitution C T missense_variant E1720K 5158G>A BLCA-US 20 61512446 61512446 single base substitution G A missense_variant S1621L 4862C>T BLCA-US 20 61512799 61512799 single base substitution C T synonymous_variant Q1503Q 4509G>A BLCA-US 20 61512978 61512978 single base substitution G A synonymous_variant L1444L 4330C>T BLCA-US 20 61512984 61512984 single base substitution C G missense_variant D1442H 4324G>C BLCA-US 20 61513072 61513072 single base substitution C G missense_variant R1412S 4236G>C BLCA-US 20 61513083 61513083 single base substitution C T missense_variant E1409K 4225G>A BLCA-US 20 61513532 61513532 single base substitution C A missense_variant G1259V 3776G>T BLCA-US 20 61524224 61524224 single base substitution C G missense_variant Q1064H 3192G>C BLCA-US 20 61525841 61525841 single base substitution G A synonymous_variant V832V 2496C>T BLCA-US 20 61526493 61526493 single base substitution C G missense_variant E747Q 2239G>C BLCA-US 20 61527666 61527666 single base substitution A T missense_variant F711L 2133T>A BLCA-US 20 61537316 61537316 single base substitution G A missense_variant S504L 1511C>T BLCA-US 20 61541160 61541160 single base substitution G A missense_variant T351I 1052C>T BLCA-US 20 61541311 61541311 single base substitution C T missense_variant E301K 901G>A BLCA-US 20 61572869 61572869 single base substitution A G upstream_gene_variant BRCA-EU 20 61504738 61504738 single base substitution C G downstream_gene_variant BRCA-EU 20 61505152 61505153 deletion of <=200bp AA - downstream_gene_variant BRCA-EU 20 61505320 61505320 single base substitution C A downstream_gene_variant BRCA-EU 20 61505320 61505320 single base substitution C T downstream_gene_variant BRCA-EU 20 61506093 61506093 single base substitution G A downstream_gene_variant BRCA-EU 20 61508105 61508105 single base substitution G A downstream_gene_variant BRCA-EU 20 61508668 61508668 single base substitution G A downstream_gene_variant BRCA-EU 20 61509394 61509394 single base substitution C G 3_prime_UTR_variant BRCA-EU 20 61510920 61510920 single base substitution C T missense_variant D2130N 6388G>A BRCA-EU 20 61511346 61511346 single base substitution G T missense_variant Q1988K 5962C>A BRCA-EU 20 61512074 61512074 deletion of <=200bp C - frameshift_variant G1745 BRCA-EU 20 61512160 61512160 single base substitution T G synonymous_variant A1716A 5148A>C BRCA-EU 20 61514570 61514570 single base substitution C A downstream_gene_variant BRCA-EU 20 61514570 61514570 single base substitution C A intron_variant BRCA-EU 20 61514678 61514678 single base substitution G C downstream_gene_variant BRCA-EU 20 61514678 61514678 single base substitution G C intron_variant BRCA-EU 20 61515363 61515363 single base substitution A C downstream_gene_variant BRCA-EU 20 61515363 61515363 single base substitution A C intron_variant BRCA-EU 20 61515430 61515430 single base substitution C A downstream_gene_variant BRCA-EU 20 61515430 61515430 single base substitution C A intron_variant BRCA-EU 20 61515586 61515586 single base substitution A C downstream_gene_variant BRCA-EU 20 61515586 61515586 single base substitution A C intron_variant BRCA-EU 20 61515587 61515587 single base substitution C T downstream_gene_variant BRCA-EU 20 61515587 61515587 single base substitution C T intron_variant BRCA-EU 20 61515931 61515931 single base substitution A C downstream_gene_variant BRCA-EU 20 61515931 61515931 single base substitution A C intron_variant BRCA-EU 20 61518082 61518082 single base substitution T C downstream_gene_variant BRCA-EU 20 61518082 61518082 single base substitution T C intron_variant BRCA-EU 20 61518257 61518257 single base substitution C A downstream_gene_variant BRCA-EU 20 61518257 61518257 single base substitution C A intron_variant BRCA-EU 20 61519751 61519751 single base substitution C G 3_prime_UTR_variant BRCA-EU 20 61519751 61519751 single base substitution C G intron_variant BRCA-EU 20 61520540 61520540 single base substitution C A 3_prime_UTR_variant BRCA-EU 20 61520540 61520540 single base substitution C A intron_variant BRCA-EU 20 61520541 61520541 single base substitution A G 3_prime_UTR_variant BRCA-EU 20 61520541 61520541 single base substitution A G intron_variant BRCA-EU 20 61520985 61520985 single base substitution C G 3_prime_UTR_variant BRCA-EU 20 61520985 61520985 single base substitution C G intron_variant BRCA-EU 20 61521881 61521881 single base substitution C G 3_prime_UTR_variant BRCA-EU 20 61521881 61521881 single base substitution C G intron_variant BRCA-EU 20 61522187 61522187 single base substitution G A 3_prime_UTR_variant BRCA-EU 20 61522187 61522187 single base substitution G A intron_variant BRCA-EU 20 61522305 61522305 single base substitution C T missense_variant R1183H 3548G>A BRCA-EU 20 61522305 61522305 single base substitution C T splice_region_variant BRCA-EU 20 61523096 61523096 single base substitution G A intron_variant BRCA-EU 20 61523282 61523282 single base substitution T C intron_variant BRCA-EU 20 61523875 61523875 single base substitution C T intron_variant BRCA-EU 20 61524839 61524839 single base substitution A T intron_variant BRCA-EU 20 61525844 61525844 single base substitution G A synonymous_variant D831D 2493C>T BRCA-EU 20 61525989 61525989 single base substitution G A intron_variant BRCA-EU 20 61526266 61526266 single base substitution C G missense_variant V778L 2332G>C BRCA-EU 20 61527396 61527396 single base substitution G A intron_variant BRCA-EU 20 61527453 61527462 deletion of <=200bp AGGATCACAG - intron_variant BRCA-EU 20 61527471 61527471 single base substitution G C intron_variant BRCA-EU 20 61527483 61527483 single base substitution C G intron_variant BRCA-EU 20 61527500 61527500 single base substitution C A intron_variant BRCA-EU 20 61527504 61527504 single base substitution C A intron_variant BRCA-EU 20 61528057 61528057 single base substitution T A missense_variant K627M 1880A>T BRCA-EU 20 61528315 61528315 single base substitution G A missense_variant A541V 1622C>T BRCA-EU 20 61529167 61529167 single base substitution G A intron_variant BRCA-EU 20 61530444 61530444 single base substitution C T intron_variant BRCA-EU 20 61531388 61531388 single base substitution C G downstream_gene_variant BRCA-EU 20 61531388 61531388 single base substitution C G intron_variant BRCA-EU 20 61532150 61532150 single base substitution C T downstream_gene_variant BRCA-EU 20 61532150 61532150 single base substitution C T intron_variant BRCA-EU 20 61533482 61533510 deletion of <=200bp GATGGACAGGGGCACCACGGGACGGTGCT - downstream_gene_variant BRCA-EU 20 61533482 61533510 deletion of <=200bp GATGGACAGGGGCACCACGGGACGGTGCT - intron_variant BRCA-EU 20 61533866 61533866 single base substitution C G downstream_gene_variant BRCA-EU 20 61533866 61533866 single base substitution C G intron_variant BRCA-EU 20 61533871 61533871 single base substitution G A downstream_gene_variant BRCA-EU 20 61533871 61533871 single base substitution G A intron_variant BRCA-EU 20 61534925 61534925 single base substitution C T downstream_gene_variant BRCA-EU 20 61534925 61534925 single base substitution C T intron_variant BRCA-EU 20 61536984 61536984 single base substitution A G 3_prime_UTR_variant BRCA-EU 20 61536984 61536984 single base substitution A G intron_variant BRCA-EU 20 61537266 61537266 single base substitution C T missense_variant A521T 1561G>A BRCA-EU 20 61537850 61537850 single base substitution A T intron_variant BRCA-EU 20 61538235 61538235 single base substitution G A intron_variant BRCA-EU 20 61541256 61541256 single base substitution C T missense_variant C319Y 956G>A BRCA-EU 20 61541408 61541408 single base substitution G A intron_variant BRCA-EU 20 61541875 61541875 single base substitution G A intron_variant BRCA-EU 20 61542405 61542405 single base substitution C T missense_variant R187H 560G>A BRCA-EU 20 61542566 61542566 single base substitution C T synonymous_variant K133K 399G>A BRCA-EU 20 61543166 61543185 deletion of <=200bp AAACAACTAACGTTTAGACA - intron_variant BRCA-EU 20 61543391 61543391 single base substitution C T intron_variant BRCA-EU 20 61544543 61544543 single base substitution C A intron_variant BRCA-EU 20 61545256 61545256 single base substitution C A intron_variant BRCA-EU 20 61546968 61546968 single base substitution G A intron_variant BRCA-EU 20 61546968 61546968 single base substitution G A upstream_gene_variant BRCA-EU 20 61547018 61547018 single base substitution A T intron_variant BRCA-EU 20 61547018 61547018 single base substitution A T upstream_gene_variant BRCA-EU 20 61547671 61547671 deletion of <=200bp T - intron_variant BRCA-EU 20 61547671 61547671 deletion of <=200bp T - upstream_gene_variant BRCA-EU 20 61547892 61547892 single base substitution C T intron_variant BRCA-EU 20 61547892 61547892 single base substitution C T upstream_gene_variant BRCA-EU 20 61548496 61548496 single base substitution C T intron_variant BRCA-EU 20 61548496 61548496 single base substitution C T upstream_gene_variant BRCA-EU 20 61550479 61550479 single base substitution G A intron_variant BRCA-EU 20 61550479 61550479 single base substitution G A upstream_gene_variant BRCA-EU 20 61550617 61550617 single base substitution G C intron_variant BRCA-EU 20 61550617 61550617 single base substitution G C upstream_gene_variant BRCA-EU 20 61550696 61550696 single base substitution G A intron_variant BRCA-EU 20 61550696 61550696 single base substitution G A upstream_gene_variant BRCA-EU 20 61550846 61550846 single base substitution C T intron_variant BRCA-EU 20 61551019 61551019 single base substitution G C intron_variant BRCA-EU 20 61551784 61551784 single base substitution G C intron_variant BRCA-EU 20 61551861 61551861 single base substitution G T intron_variant BRCA-EU 20 61553859 61553859 deletion of <=200bp G - intron_variant BRCA-EU 20 61554477 61554477 single base substitution C T intron_variant BRCA-EU 20 61554597 61554597 single base substitution G A intron_variant BRCA-EU 20 61555015 61555015 single base substitution C T intron_variant BRCA-EU 20 61556180 61556180 single base substitution G C intron_variant BRCA-EU 20 61560481 61560481 single base substitution G A intron_variant BRCA-EU 20 61560481 61560481 single base substitution G A upstream_gene_variant BRCA-EU 20 61560778 61560778 single base substitution A T intron_variant BRCA-EU 20 61560778 61560778 single base substitution A T upstream_gene_variant BRCA-EU 20 61561312 61561316 deletion of <=200bp GCGGT - intron_variant BRCA-EU 20 61561312 61561316 deletion of <=200bp GCGGT - upstream_gene_variant BRCA-EU 20 61561585 61561585 deletion of <=200bp C - intron_variant BRCA-EU 20 61561585 61561585 deletion of <=200bp C - upstream_gene_variant BRCA-EU 20 61561734 61561734 single base substitution G A intron_variant BRCA-EU 20 61561734 61561734 single base substitution G A upstream_gene_variant BRCA-EU 20 61561872 61561872 single base substitution G C intron_variant BRCA-EU 20 61561872 61561872 single base substitution G C upstream_gene_variant BRCA-EU 20 61562498 61562498 single base substitution G A intron_variant BRCA-EU 20 61562498 61562498 single base substitution G A upstream_gene_variant BRCA-EU 20 61563707 61563707 single base substitution C T intron_variant BRCA-EU 20 61564404 61564404 single base substitution A T intron_variant BRCA-EU 20 61564568 61564568 deletion of <=200bp A - intron_variant BRCA-EU 20 61564733 61564733 single base substitution C A intron_variant BRCA-EU 20 61565291 61565291 single base substitution C G intron_variant BRCA-EU 20 61565795 61565795 single base substitution T G intron_variant BRCA-EU 20 61566030 61566030 single base substitution A G intron_variant BRCA-EU 20 61566643 61566643 single base substitution C T intron_variant BRCA-EU 20 61566937 61566937 single base substitution G A intron_variant BRCA-EU 20 61568548 61568548 single base substitution C T intron_variant BRCA-EU 20 61568574 61568574 single base substitution C T intron_variant BRCA-EU 20 61568602 61568602 single base substitution C T intron_variant BRCA-EU 20 61570084 61570086 deletion of <=200bp AGT - upstream_gene_variant BRCA-EU 20 61570373 61570373 single base substitution G C upstream_gene_variant BRCA-EU 20 61570403 61570403 single base substitution G C upstream_gene_variant BRCA-EU 20 61571125 61571125 single base substitution C G upstream_gene_variant BRCA-EU 20 61571399 61571399 deletion of <=200bp A - upstream_gene_variant BRCA-EU 20 61571953 61571953 single base substitution G A upstream_gene_variant BRCA-EU 20 61572283 61572283 single base substitution G A upstream_gene_variant BRCA-EU 20 61573054 61573054 single base substitution T C upstream_gene_variant BRCA-EU 20 61573616 61573616 single base substitution A G upstream_gene_variant BRCA-FR 20 61506093 61506093 single base substitution G A downstream_gene_variant BRCA-FR 20 61514678 61514678 single base substitution G C downstream_gene_variant BRCA-FR 20 61514678 61514678 single base substitution G C intron_variant BRCA-FR 20 61527471 61527471 single base substitution G C intron_variant BRCA-FR 20 61533866 61533866 single base substitution C G downstream_gene_variant BRCA-FR 20 61533866 61533866 single base substitution C G intron_variant BRCA-FR 20 61536659 61536659 single base substitution C T 3_prime_UTR_variant BRCA-FR 20 61536659 61536659 single base substitution C T downstream_gene_variant BRCA-FR 20 61536659 61536659 single base substitution C T intron_variant BRCA-FR 20 61537266 61537266 single base substitution C T missense_variant A521T 1561G>A BRCA-FR 20 61547018 61547018 single base substitution A T intron_variant BRCA-FR 20 61547018 61547018 single base substitution A T upstream_gene_variant BRCA-FR 20 61556180 61556180 single base substitution G C intron_variant BRCA-FR 20 61566643 61566643 single base substitution C T intron_variant BRCA-FR 20 61570403 61570403 single base substitution G C upstream_gene_variant BRCA-KR 20 61511746 61511746 single base substitution C T synonymous_variant E1854E 5562G>A BRCA-UK 20 61510956 61510956 single base substitution C T missense_variant E2118K 6352G>A BRCA-UK 20 61511899 61511899 single base substitution C A missense_variant Q1803H 5409G>T BRCA-UK 20 61512069 61512069 single base substitution G C missense_variant Q1747E 5239C>G BRCA-UK 20 61513050 61513050 single base substitution C T missense_variant E1420K 4258G>A BRCA-UK 20 61526405 61526405 single base substitution C T missense_variant R776K 2327G>A BRCA-UK 20 61532150 61532150 single base substitution C T downstream_gene_variant BRCA-UK 20 61532150 61532150 single base substitution C T intron_variant BRCA-UK 20 61538235 61538235 single base substitution G A intron_variant BRCA-UK 20 61541304 61541304 single base substitution C T missense_variant R303Q 908G>A BRCA-US 20 61512736 61512736 single base substitution T G synonymous_variant P1524P 4572A>C BRCA-US 20 61512792 61512792 single base substitution C T missense_variant A1506T 4516G>A BRCA-US 20 61513156 61513156 single base substitution T C synonymous_variant P1384P 4152A>G BRCA-US 20 61522371 61522371 single base substitution A C missense_variant L1161R 3482T>G BRCA-US 20 61523338 61523338 single base substitution C G splice_donor_variant BRCA-US 20 61524224 61524224 single base substitution C T synonymous_variant Q1064Q 3192G>A BRCA-US 20 61525826 61525826 single base substitution C G missense_variant L837F 2511G>C BRCA-US 20 61528246 61528246 single base substitution C G missense_variant R564T 1691G>C BRCA-US 20 61537437 61537437 insertion of <=200bp - T frameshift_variant S464Y? BRCA-US 20 61537438 61537438 single base substitution G T synonymous_variant I463I 1389C>A BRCA-US 20 61542181 61542181 single base substitution C T missense_variant E262K 784G>A BRCA-US 20 61542268 61542268 single base substitution C T missense_variant D233N 697G>A BRCA-US 20 61542482 61542482 single base substitution C T synonymous_variant L161L 483G>A BRCA-US 20 61542562 61542562 single base substitution G A stop_gained R135* 403C>T BRCA-US 20 61542600 61542600 single base substitution C G missense_variant R122T 365G>C BRCA-US 20 61542836 61542836 single base substitution C T synonymous_variant A43A 129G>A BRCA-US 20 61542888 61542888 single base substitution G A missense_variant T26I 77C>T BRCA-US 20 61572857 61572857 single base substitution G A upstream_gene_variant BRCA-US 20 61572953 61572953 single base substitution C T upstream_gene_variant BTCA-JP 20 61510947 61510947 single base substitution G A stop_gained R2121* 6361C>T BTCA-JP 20 61512095 61512095 deletion of <=200bp G - frameshift_variant P1738 BTCA-JP 20 61512381 61512381 single base substitution G A missense_variant R1643C 4927C>T BTCA-JP 20 61512914 61512914 single base substitution G A missense_variant A1465V 4394C>T BTCA-JP 20 61512921 61512921 single base substitution G A missense_variant P1463S 4387C>T BTCA-JP 20 61513097 61513097 single base substitution C T missense_variant R1404Q 4211G>A BTCA-JP 20 61526132 61526132 single base substitution C T intron_variant BTCA-JP 20 61526495 61526495 single base substitution C T missense_variant R746H 2237G>A CESC-US 20 61510621 61510621 single base substitution C T synonymous_variant S2229S 6687G>A CESC-US 20 61511181 61511181 single base substitution C T missense_variant E2043K 6127G>A CESC-US 20 61512312 61512312 single base substitution C T missense_variant G1666S 4996G>A CESC-US 20 61512828 61512828 single base substitution C G missense_variant E1494Q 4480G>C CESC-US 20 61513055 61513055 single base substitution G T missense_variant A1418E 4253C>A CESC-US 20 61525016 61525016 single base substitution A T splice_donor_variant CESC-US 20 61525382 61525382 single base substitution C T missense_variant E913K 2737G>A CESC-US 20 61526236 61526236 single base substitution C T missense_variant E788K 2362G>A CESC-US 20 61527728 61527728 single base substitution C G missense_variant D691H 2071G>C CESC-US 20 61542823 61542823 single base substitution G A synonymous_variant L48L 142C>T CLLE-ES 20 61549699 61549699 single base substitution T G intron_variant CLLE-ES 20 61549699 61549699 single base substitution T G upstream_gene_variant COAD-US 20 61510712 61510712 single base substitution C T missense_variant R2199Q 6596G>A COAD-US 20 61510857 61510857 single base substitution G A missense_variant R2151W 6451C>T COAD-US 20 61510959 61510959 single base substitution G A missense_variant R2117C 6349C>T COAD-US 20 61511050 61511050 single base substitution C A missense_variant R2086S 6258G>T COAD-US 20 61511124 61511124 single base substitution C T missense_variant D2062N 6184G>A COAD-US 20 61511207 61511207 single base substitution G A missense_variant P2034L 6101C>T COAD-US 20 61511242 61511242 single base substitution G A synonymous_variant G2022G 6066C>T COAD-US 20 61511257 61511257 single base substitution C A missense_variant Q2017H 6051G>T COAD-US 20 61511496 61511496 single base substitution G A missense_variant R1938W 5812C>T COAD-US 20 61511626 61511626 single base substitution C T synonymous_variant R1894R 5682G>A COAD-US 20 61511656 61511656 single base substitution G A synonymous_variant G1884G 5652C>T COAD-US 20 61512095 61512095 single base substitution G A missense_variant P1738L 5213C>T COAD-US 20 61512102 61512102 single base substitution G A missense_variant L1736F 5206C>T COAD-US 20 61512376 61512376 single base substitution G A synonymous_variant P1644P 4932C>T COAD-US 20 61512412 61512412 single base substitution G A synonymous_variant D1632D 4896C>T COAD-US 20 61512606 61512606 single base substitution T C missense_variant T1568A 4702A>G COAD-US 20 61513092 61513092 single base substitution G A missense_variant R1406W 4216C>T COAD-US 20 61513370 61513370 single base substitution G A missense_variant P1313L 3938C>T COAD-US 20 61513681 61513681 single base substitution G A downstream_gene_variant COAD-US 20 61513681 61513681 single base substitution G A synonymous_variant D1209D 3627C>T COAD-US 20 61523352 61523352 single base substitution G A missense_variant S1111F 3332C>T COAD-US 20 61525830 61525830 single base substitution A G missense_variant M836T 2507T>C COAD-US 20 61526505 61526505 single base substitution G A missense_variant R743C 2227C>T COAD-US 20 61527666 61527666 deletion of <=200bp A - frameshift_variant F711 COAD-US 20 61527946 61527946 single base substitution G A missense_variant S664L 1991C>T COAD-US 20 61528199 61528199 single base substitution T A missense_variant T580S 1738A>T COAD-US 20 61528256 61528256 single base substitution G A missense_variant P561S 1681C>T COAD-US 20 61538507 61538507 single base substitution C T missense_variant G456S 1366G>A COAD-US 20 61538649 61538649 single base substitution G A synonymous_variant P408P 1224C>T COAD-US 20 61542279 61542279 single base substitution G A missense_variant A229V 686C>T COAD-US 20 61542717 61542717 single base substitution C T missense_variant R83H 248G>A COCA-CN 20 61506666 61506666 single base substitution G C downstream_gene_variant COCA-CN 20 61510467 61510467 single base substitution A C 3_prime_UTR_variant COCA-CN 20 61510582 61510582 single base substitution C T 3_prime_UTR_variant COCA-CN 20 61510951 61510951 single base substitution G A synonymous_variant R2119R 6357C>T COCA-CN 20 61511131 61511131 single base substitution G A synonymous_variant P2059P 6177C>T COCA-CN 20 61511331 61511331 single base substitution G A missense_variant R1993W 5977C>T COCA-CN 20 61511655 61511655 single base substitution C T missense_variant A1885T 5653G>A COCA-CN 20 61511770 61511770 single base substitution C A missense_variant K1846N 5538G>T COCA-CN 20 61512243 61512243 single base substitution C T missense_variant A1689T 5065G>A COCA-CN 20 61512290 61512290 single base substitution G A missense_variant P1673L 5018C>T COCA-CN 20 61512508 61512508 single base substitution G A synonymous_variant L1600L 4800C>T COCA-CN 20 61512901 61512901 single base substitution C T synonymous_variant T1469T 4407G>A COCA-CN 20 61513097 61513097 single base substitution C T missense_variant R1404Q 4211G>A COCA-CN 20 61513558 61513558 single base substitution G A synonymous_variant D1250D 3750C>T COCA-CN 20 61513597 61513597 single base substitution C T downstream_gene_variant COCA-CN 20 61513597 61513597 single base substitution C T synonymous_variant S1237S 3711G>A COCA-CN 20 61527378 61527378 single base substitution G A intron_variant COCA-CN 20 61538478 61538478 single base substitution G A intron_variant COCA-CN 20 61540944 61540944 single base substitution G A intron_variant COCA-CN 20 61542722 61542722 single base substitution C T synonymous_variant A81A 243G>A COCA-CN 20 61542805 61542805 single base substitution G A stop_gained Q54* 160C>T COCA-CN 20 61572760 61572760 single base substitution C T upstream_gene_variant COCA-CN 20 61572887 61572887 single base substitution G A upstream_gene_variant EOPC-DE 20 61530243 61530243 single base substitution T C intron_variant EOPC-DE 20 61544951 61544951 single base substitution T A intron_variant ESAD-UK 20 61504696 61504696 single base substitution G T downstream_gene_variant ESAD-UK 20 61507586 61507586 single base substitution G T downstream_gene_variant ESAD-UK 20 61511368 61511368 single base substitution G A synonymous_variant N1980N 5940C>T ESAD-UK 20 61511785 61511785 single base substitution T C synonymous_variant Q1841Q 5523A>G ESAD-UK 20 61512760 61512760 single base substitution C A synonymous_variant V1516V 4548G>T ESAD-UK 20 61516149 61516149 single base substitution A G downstream_gene_variant ESAD-UK 20 61516149 61516149 single base substitution A G intron_variant ESAD-UK 20 61517881 61517881 single base substitution G A downstream_gene_variant ESAD-UK 20 61517881 61517881 single base substitution G A intron_variant ESAD-UK 20 61520006 61520006 insertion of <=200bp - AC 3_prime_UTR_variant ESAD-UK 20 61520006 61520006 insertion of <=200bp - AC intron_variant ESAD-UK 20 61520868 61520868 single base substitution C A 3_prime_UTR_variant ESAD-UK 20 61520868 61520868 single base substitution C A intron_variant ESAD-UK 20 61521649 61521649 single base substitution G A 3_prime_UTR_variant ESAD-UK 20 61521649 61521649 single base substitution G A intron_variant ESAD-UK 20 61522934 61522934 single base substitution C T intron_variant ESAD-UK 20 61523449 61523449 single base substitution G A intron_variant ESAD-UK 20 61525857 61525857 single base substitution G A missense_variant A827V 2480C>T ESAD-UK 20 61526584 61526584 single base substitution G A intron_variant ESAD-UK 20 61526696 61526696 single base substitution C A intron_variant ESAD-UK 20 61528915 61528915 single base substitution C T intron_variant ESAD-UK 20 61529128 61529128 single base substitution C T intron_variant ESAD-UK 20 61529142 61529142 single base substitution G A intron_variant ESAD-UK 20 61532034 61532034 single base substitution A G downstream_gene_variant ESAD-UK 20 61532034 61532034 single base substitution A G intron_variant ESAD-UK 20 61532884 61532884 single base substitution T G downstream_gene_variant ESAD-UK 20 61532884 61532884 single base substitution T G intron_variant ESAD-UK 20 61533027 61533027 single base substitution G A downstream_gene_variant ESAD-UK 20 61533027 61533027 single base substitution G A intron_variant ESAD-UK 20 61533356 61533356 single base substitution G A downstream_gene_variant ESAD-UK 20 61533356 61533356 single base substitution G A intron_variant ESAD-UK 20 61533416 61533416 single base substitution A G downstream_gene_variant ESAD-UK 20 61533416 61533416 single base substitution A G intron_variant ESAD-UK 20 61533452 61533452 single base substitution T A downstream_gene_variant ESAD-UK 20 61533452 61533452 single base substitution T A intron_variant ESAD-UK 20 61534186 61534186 single base substitution G A downstream_gene_variant ESAD-UK 20 61534186 61534186 single base substitution G A intron_variant ESAD-UK 20 61537121 61537121 single base substitution C T 3_prime_UTR_variant ESAD-UK 20 61537121 61537121 single base substitution C T intron_variant ESAD-UK 20 61537852 61537852 single base substitution C T intron_variant ESAD-UK 20 61538160 61538160 single base substitution C A intron_variant ESAD-UK 20 61539535 61539535 single base substitution G A intron_variant ESAD-UK 20 61542145 61542145 single base substitution G A missense_variant R274C 820C>T ESAD-UK 20 61542422 61542422 single base substitution C G synonymous_variant L181L 543G>C ESAD-UK 20 61547639 61547639 single base substitution C G intron_variant ESAD-UK 20 61547639 61547639 single base substitution C G upstream_gene_variant ESAD-UK 20 61551147 61551147 single base substitution C T intron_variant ESAD-UK 20 61553572 61553572 insertion of <=200bp - AC intron_variant ESAD-UK 20 61553593 61553593 single base substitution T C intron_variant ESAD-UK 20 61553671 61553671 single base substitution C A intron_variant ESAD-UK 20 61554220 61554220 single base substitution G A intron_variant ESAD-UK 20 61554371 61554371 single base substitution G T intron_variant ESAD-UK 20 61554824 61554824 single base substitution C A intron_variant ESAD-UK 20 61555338 61555338 single base substitution C G intron_variant ESAD-UK 20 61555703 61555703 deletion of <=200bp T - intron_variant ESAD-UK 20 61556053 61556053 single base substitution C A intron_variant ESAD-UK 20 61556199 61556199 single base substitution C G intron_variant ESAD-UK 20 61556528 61556528 single base substitution G C intron_variant ESAD-UK 20 61556717 61556717 single base substitution C G intron_variant ESAD-UK 20 61557945 61557964 deletion of <=200bp CTGCGAAGCCCGGCCCCGGA - intron_variant ESAD-UK 20 61557945 61557964 deletion of <=200bp CTGCGAAGCCCGGCCCCGGA - upstream_gene_variant ESAD-UK 20 61559151 61559151 single base substitution C A intron_variant ESAD-UK 20 61559151 61559151 single base substitution C A upstream_gene_variant ESAD-UK 20 61559152 61559152 single base substitution G A intron_variant ESAD-UK 20 61559152 61559152 single base substitution G A upstream_gene_variant ESAD-UK 20 61559986 61559986 single base substitution C G intron_variant ESAD-UK 20 61559986 61559986 single base substitution C G upstream_gene_variant ESAD-UK 20 61559994 61559994 single base substitution A C intron_variant ESAD-UK 20 61559994 61559994 single base substitution A C upstream_gene_variant ESAD-UK 20 61560581 61560581 single base substitution C A intron_variant ESAD-UK 20 61560581 61560581 single base substitution C A upstream_gene_variant ESAD-UK 20 61561363 61561363 single base substitution C G intron_variant ESAD-UK 20 61561363 61561363 single base substitution C G upstream_gene_variant ESAD-UK 20 61561997 61561997 single base substitution G A intron_variant ESAD-UK 20 61561997 61561997 single base substitution G A upstream_gene_variant ESAD-UK 20 61562543 61562543 single base substitution C T intron_variant ESAD-UK 20 61562543 61562543 single base substitution C T upstream_gene_variant ESAD-UK 20 61563539 61563539 single base substitution A T intron_variant ESAD-UK 20 61563735 61563735 single base substitution T G intron_variant ESAD-UK 20 61564047 61564047 single base substitution G C intron_variant ESAD-UK 20 61564809 61564809 single base substitution C T intron_variant ESAD-UK 20 61566671 61566671 single base substitution C T intron_variant ESAD-UK 20 61568061 61568061 single base substitution C G intron_variant ESAD-UK 20 61571609 61571609 single base substitution T A upstream_gene_variant ESAD-UK 20 61572377 61572377 single base substitution G C upstream_gene_variant ESAD-UK 20 61572633 61572633 single base substitution C T upstream_gene_variant ESAD-UK 20 61572779 61572779 single base substitution C T upstream_gene_variant ESAD-UK 20 61572890 61572890 single base substitution A G upstream_gene_variant ESCA-CN 20 61513201 61513201 single base substitution C G missense_variant Q1369H 4107G>C ESCA-CN 20 61513639 61513639 single base substitution C T downstream_gene_variant ESCA-CN 20 61513639 61513639 single base substitution C T synonymous_variant A1223A 3669G>A ESCA-CN 20 61526023 61526023 single base substitution T G intron_variant ESCA-CN 20 61527736 61527736 single base substitution T G missense_variant D688A 2063A>C ESCA-CN 20 61528312 61528312 single base substitution G T missense_variant A542E 1625C>A ESCA-CN 20 61538547 61538547 single base substitution C G missense_variant K442N 1326G>C ESCA-CN 20 61542620 61542620 single base substitution C T synonymous_variant V115V 345G>A GBM-US 20 61511189 61511189 single base substitution C T missense_variant R2040H 6119G>A GBM-US 20 61512320 61512320 single base substitution G A missense_variant P1663L 4988C>T GBM-US 20 61542712 61542712 single base substitution C T missense_variant G85S 253G>A KIRC-US 20 61513427 61513438 deletion of <=200bp GCTGCTGTTGTG - disruptive_inframe_deletion ATTAA1290A KIRC-US 20 61526431 61526431 single base substitution A G synonymous_variant L767L 2301T>C KIRC-US 20 61527636 61527636 single base substitution G A synonymous_variant Y721Y 2163C>T KIRC-US 20 61537212 61537212 single base substitution G A intron_variant KIRC-US 20 61537212 61537212 single base substitution G A synonymous_variant L539L 1615C>T KIRP-US 20 61510808 61510808 deletion of <=200bp T - frameshift_variant K2167 KIRP-US 20 61537401 61537401 insertion of <=200bp - T frameshift_variant E476E? LAML-KR 20 61528306 61528306 single base substitution A G missense_variant M544T 1631T>C LAML-KR 20 61536938 61536938 single base substitution G A 3_prime_UTR_variant LAML-KR 20 61536938 61536938 single base substitution G A intron_variant LAML-KR 20 61536938 61536938 single base substitution G A missense_variant S535L 1604C>T LGG-US 20 61511961 61511961 single base substitution C T missense_variant E1783K 5347G>A LGG-US 20 61511992 61511992 single base substitution C T synonymous_variant P1772P 5316G>A LGG-US 20 61527924 61527924 single base substitution C T synonymous_variant R671R 2013G>A LICA-CN 20 61511969 61511969 single base substitution G A missense_variant P1780L 5339C>T LICA-CN 20 61512427 61512427 single base substitution C A synonymous_variant A1627A 4881G>T LICA-CN 20 61542631 61542631 single base substitution C A stop_gained E112* 334G>T LICA-FR 20 61512727 61512727 single base substitution C T synonymous_variant S1527S 4581G>A LICA-FR 20 61525160 61525160 single base substitution C G missense_variant D987H 2959G>C LICA-FR 20 61525506 61525506 insertion of <=200bp - T frameshift_variant K871K? LICA-FR 20 61527931 61527931 single base substitution T C missense_variant Q669R 2006A>G LICA-FR 20 61536133 61536140 deletion of <=200bp AAAAAAAA - downstream_gene_variant LICA-FR 20 61536133 61536140 deletion of <=200bp AAAAAAAA - intron_variant LICA-FR 20 61537349 61537349 single base substitution C T missense_variant G493E 1478G>A LICA-FR 20 61559254 61559254 single base substitution A C intron_variant LICA-FR 20 61559254 61559254 single base substitution A C upstream_gene_variant LICA-FR 20 61564527 61564527 single base substitution C A intron_variant LIHC-US 20 61511712 61511712 single base substitution C T missense_variant A1866T 5596G>A LIHC-US 20 61511798 61511798 single base substitution A C missense_variant V1837G 5510T>G LIHC-US 20 61511821 61511821 single base substitution A G synonymous_variant S1829S 5487T>C LIHC-US 20 61512777 61512777 single base substitution T C missense_variant M1511V 4531A>G LIHC-US 20 61512904 61512904 single base substitution C A synonymous_variant A1468A 4404G>T LIHC-US 20 61522428 61522428 single base substitution C T missense_variant S1142N 3425G>A LIHC-US 20 61525548 61525548 single base substitution T A splice_acceptor_variant LIHC-US 20 61528282 61528282 single base substitution G A missense_variant P552L 1655C>T LINC-JP 20 61512298 61512298 single base substitution G A synonymous_variant P1670P 5010C>T LINC-JP 20 61517852 61517852 single base substitution C G downstream_gene_variant LINC-JP 20 61517852 61517852 single base substitution C G intron_variant LINC-JP 20 61524212 61524212 single base substitution T C synonymous_variant K1068K 3204A>G LINC-JP 20 61524300 61524300 single base substitution C A missense_variant R1039L 3116G>T LINC-JP 20 61525202 61525202 single base substitution T C missense_variant S973G 2917A>G LINC-JP 20 61525801 61525801 single base substitution C A missense_variant A846S 2536G>T LINC-JP 20 61537428 61537428 single base substitution G T missense_variant H467N 1399C>A LINC-JP 20 61538060 61538062 deletion of <=200bp AAA - intron_variant LINC-JP 20 61538072 61538072 deletion of <=200bp G - intron_variant LINC-JP 20 61542837 61542837 single base substitution G A missense_variant A43V 128C>T LINC-JP 20 61543855 61543855 deletion of <=200bp T - intron_variant LINC-JP 20 61546500 61546500 single base substitution A C intron_variant LINC-JP 20 61546500 61546500 single base substitution A C upstream_gene_variant LINC-JP 20 61553463 61553463 single base substitution C T intron_variant LINC-JP 20 61556270 61556270 deletion of <=200bp G - intron_variant LINC-JP 20 61557624 61557624 single base substitution C T intron_variant LINC-JP 20 61561047 61561047 single base substitution G A intron_variant LINC-JP 20 61561047 61561047 single base substitution G A upstream_gene_variant LIRI-JP 20 61506439 61506439 single base substitution C A downstream_gene_variant LIRI-JP 20 61507223 61507223 single base substitution C A downstream_gene_variant LIRI-JP 20 61507234 61507234 single base substitution G C downstream_gene_variant LIRI-JP 20 61514721 61514721 single base substitution G C downstream_gene_variant LIRI-JP 20 61514721 61514721 single base substitution G C intron_variant LIRI-JP 20 61515423 61515423 single base substitution T C downstream_gene_variant LIRI-JP 20 61515423 61515423 single base substitution T C intron_variant LIRI-JP 20 61516761 61516761 single base substitution T C downstream_gene_variant LIRI-JP 20 61516761 61516761 single base substitution T C intron_variant LIRI-JP 20 61518627 61518627 single base substitution A T 3_prime_UTR_variant LIRI-JP 20 61518627 61518627 single base substitution A T intron_variant LIRI-JP 20 61518642 61518642 single base substitution C T 3_prime_UTR_variant LIRI-JP 20 61518642 61518642 single base substitution C T intron_variant LIRI-JP 20 61518728 61518728 single base substitution G T 3_prime_UTR_variant LIRI-JP 20 61518728 61518728 single base substitution G T intron_variant LIRI-JP 20 61518830 61518830 single base substitution G A 3_prime_UTR_variant LIRI-JP 20 61518830 61518830 single base substitution G A intron_variant LIRI-JP 20 61518831 61518831 single base substitution C T 3_prime_UTR_variant LIRI-JP 20 61518831 61518831 single base substitution C T intron_variant LIRI-JP 20 61525254 61525254 single base substitution G A synonymous_variant S955S 2865C>T LIRI-JP 20 61526791 61526791 single base substitution C T intron_variant LIRI-JP 20 61529279 61529279 single base substitution T C intron_variant LIRI-JP 20 61529933 61529933 single base substitution T C intron_variant LIRI-JP 20 61531077 61531077 single base substitution A C intron_variant LIRI-JP 20 61532628 61532628 single base substitution T G downstream_gene_variant LIRI-JP 20 61532628 61532628 single base substitution T G intron_variant LIRI-JP 20 61533838 61533838 single base substitution C T downstream_gene_variant LIRI-JP 20 61533838 61533838 single base substitution C T intron_variant LIRI-JP 20 61533841 61533841 single base substitution G A downstream_gene_variant LIRI-JP 20 61533841 61533841 single base substitution G A intron_variant LIRI-JP 20 61534671 61534671 single base substitution G T downstream_gene_variant LIRI-JP 20 61534671 61534671 single base substitution G T intron_variant LIRI-JP 20 61535436 61535436 single base substitution A C downstream_gene_variant LIRI-JP 20 61535436 61535436 single base substitution A C intron_variant LIRI-JP 20 61536119 61536119 single base substitution A G downstream_gene_variant LIRI-JP 20 61536119 61536119 single base substitution A G intron_variant LIRI-JP 20 61540233 61540233 single base substitution T G intron_variant LIRI-JP 20 61540321 61540321 single base substitution G T intron_variant LIRI-JP 20 61543940 61543940 single base substitution A G intron_variant LIRI-JP 20 61546376 61546376 single base substitution C G intron_variant LIRI-JP 20 61546376 61546376 single base substitution C G upstream_gene_variant LIRI-JP 20 61548168 61548168 single base substitution C A intron_variant LIRI-JP 20 61548168 61548168 single base substitution C A upstream_gene_variant LIRI-JP 20 61549443 61549443 single base substitution T C intron_variant LIRI-JP 20 61549443 61549443 single base substitution T C upstream_gene_variant LIRI-JP 20 61553846 61553846 single base substitution C T intron_variant LIRI-JP 20 61554179 61554179 single base substitution G T intron_variant LIRI-JP 20 61554446 61554446 single base substitution T C intron_variant LIRI-JP 20 61554454 61554454 single base substitution A G intron_variant LIRI-JP 20 61554955 61554955 single base substitution T C intron_variant LIRI-JP 20 61561515 61561515 single base substitution C A intron_variant LIRI-JP 20 61561515 61561515 single base substitution C A upstream_gene_variant LIRI-JP 20 61568249 61568249 single base substitution C G intron_variant LIRI-JP 20 61568830 61568830 single base substitution C T intron_variant LIRI-JP 20 61570709 61570709 single base substitution A G upstream_gene_variant LIRI-JP 20 61571944 61571944 single base substitution G A upstream_gene_variant LIRI-JP 20 61572227 61572227 single base substitution T A upstream_gene_variant LIRI-JP 20 61573550 61573550 single base substitution A G upstream_gene_variant LIRI-JP 20 61573580 61573580 single base substitution T C upstream_gene_variant LIRI-JP 20 61573595 61573595 single base substitution A C upstream_gene_variant LUSC-KR 20 61505903 61505903 single base substitution G T downstream_gene_variant LUSC-KR 20 61506453 61506453 single base substitution A T downstream_gene_variant LUSC-KR 20 61506606 61506606 single base substitution C G downstream_gene_variant LUSC-KR 20 61511262 61511262 single base substitution G C missense_variant P2016A 6046C>G LUSC-KR 20 61514028 61514028 single base substitution C G downstream_gene_variant LUSC-KR 20 61514028 61514028 single base substitution C G intron_variant LUSC-KR 20 61514665 61514665 single base substitution A G downstream_gene_variant LUSC-KR 20 61514665 61514665 single base substitution A G intron_variant LUSC-KR 20 61521357 61521357 single base substitution C A 3_prime_UTR_variant LUSC-KR 20 61521357 61521357 single base substitution C A intron_variant LUSC-KR 20 61523604 61523604 single base substitution A G intron_variant LUSC-KR 20 61527146 61527146 single base substitution G C intron_variant LUSC-KR 20 61536942 61536942 single base substitution A G 3_prime_UTR_variant LUSC-KR 20 61536942 61536942 single base substitution A G intron_variant LUSC-KR 20 61536942 61536942 single base substitution A G missense_variant Y534H 1600T>C LUSC-KR 20 61540472 61540472 single base substitution C A intron_variant LUSC-KR 20 61541821 61541821 single base substitution G C intron_variant LUSC-KR 20 61545066 61545066 single base substitution G A intron_variant LUSC-KR 20 61553463 61553463 single base substitution C T intron_variant LUSC-KR 20 61553977 61553977 single base substitution C T intron_variant LUSC-KR 20 61557418 61557418 single base substitution C A intron_variant LUSC-KR 20 61568758 61568758 single base substitution C A intron_variant LUSC-KR 20 61570840 61570840 single base substitution A C upstream_gene_variant LUSC-KR 20 61571407 61571407 single base substitution A C upstream_gene_variant LUSC-KR 20 61572022 61572022 single base substitution G C upstream_gene_variant LUSC-KR 20 61573097 61573097 single base substitution A C upstream_gene_variant LUSC-KR 20 61573508 61573508 single base substitution C G upstream_gene_variant LUSC-US 20 61511697 61511697 single base substitution C T missense_variant E1871K 5611G>A LUSC-US 20 61511762 61511762 single base substitution T A missense_variant H1849L 5546A>T LUSC-US 20 61512009 61512009 single base substitution G A missense_variant H1767Y 5299C>T LUSC-US 20 61512017 61512017 single base substitution G T stop_gained S1764* 5291C>A LUSC-US 20 61512069 61512069 single base substitution G C missense_variant Q1747E 5239C>G LUSC-US 20 61512601 61512601 single base substitution C T synonymous_variant E1569E 4707G>A LUSC-US 20 61512756 61512756 single base substitution C T missense_variant D1518N 4552G>A LUSC-US 20 61512895 61512895 single base substitution G A synonymous_variant S1471S 4413C>T LUSC-US 20 61512896 61512896 single base substitution G A missense_variant S1471F 4412C>T LUSC-US 20 61513191 61513191 single base substitution C A missense_variant D1373Y 4117G>T LUSC-US 20 61513663 61513663 single base substitution C T downstream_gene_variant LUSC-US 20 61513663 61513663 single base substitution C T synonymous_variant R1215R 3645G>A LUSC-US 20 61522319 61522319 single base substitution C A missense_variant E1178D 3534G>T LUSC-US 20 61522414 61522414 single base substitution C A missense_variant G1147C 3439G>T LUSC-US 20 61525358 61525358 single base substitution G A missense_variant H921Y 2761C>T LUSC-US 20 61525406 61525406 single base substitution C T missense_variant E905K 2713G>A LUSC-US 20 61525489 61525489 single base substitution G A missense_variant S877F 2630C>T LUSC-US 20 61525784 61525784 single base substitution G A synonymous_variant L851L 2553C>T LUSC-US 20 61527695 61527695 single base substitution T C missense_variant I702V 2104A>G LUSC-US 20 61528077 61528077 single base substitution C A synonymous_variant A620A 1860G>T LUSC-US 20 61528146 61528146 single base substitution C T synonymous_variant R597R 1791G>A LUSC-US 20 61537362 61537362 single base substitution T C missense_variant S489G 1465A>G LUSC-US 20 61541126 61541126 single base substitution T G missense_variant E362D 1086A>C MALY-DE 20 61504319 61504319 single base substitution G A downstream_gene_variant MALY-DE 20 61507702 61507702 single base substitution C G downstream_gene_variant MALY-DE 20 61518840 61518840 single base substitution T C 3_prime_UTR_variant MALY-DE 20 61518840 61518840 single base substitution T C intron_variant MALY-DE 20 61519169 61519169 single base substitution G C 3_prime_UTR_variant MALY-DE 20 61519169 61519169 single base substitution G C intron_variant MALY-DE 20 61533539 61533539 single base substitution G C downstream_gene_variant MALY-DE 20 61533539 61533539 single base substitution G C intron_variant MALY-DE 20 61536278 61536278 single base substitution C T downstream_gene_variant MALY-DE 20 61536278 61536278 single base substitution C T intron_variant MALY-DE 20 61536692 61536692 deletion of <=200bp A - 3_prime_UTR_variant MALY-DE 20 61536692 61536692 deletion of <=200bp A - downstream_gene_variant MALY-DE 20 61536692 61536692 deletion of <=200bp A - intron_variant MALY-DE 20 61543914 61543914 single base substitution A G intron_variant MALY-DE 20 61562165 61562165 single base substitution G A intron_variant MALY-DE 20 61562165 61562165 single base substitution G A upstream_gene_variant MELA-AU 20 61504437 61504437 single base substitution C T downstream_gene_variant MELA-AU 20 61504556 61504557 multiple base substitution (>=2bp and <=200bp) AG GA downstream_gene_variant MELA-AU 20 61504740 61504740 single base substitution C T downstream_gene_variant MELA-AU 20 61505592 61505592 single base substitution C T downstream_gene_variant MELA-AU 20 61505886 61505886 single base substitution C T downstream_gene_variant MELA-AU 20 61506113 61506113 single base substitution T C downstream_gene_variant MELA-AU 20 61507073 61507073 single base substitution C T downstream_gene_variant MELA-AU 20 61507348 61507348 single base substitution C T downstream_gene_variant MELA-AU 20 61507628 61507628 single base substitution G A downstream_gene_variant MELA-AU 20 61508023 61508024 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 20 61508790 61508790 single base substitution G A downstream_gene_variant MELA-AU 20 61509474 61509474 single base substitution G A 3_prime_UTR_variant MELA-AU 20 61510876 61510876 single base substitution G A synonymous_variant S2144S 6432C>T MELA-AU 20 61511172 61511172 single base substitution G A missense_variant P2046S 6136C>T MELA-AU 20 61511539 61511539 single base substitution G A synonymous_variant F1923F 5769C>T MELA-AU 20 61511707 61511708 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant P1867L 5600CC>TT MELA-AU 20 61511757 61511757 single base substitution C T missense_variant E1851K 5551G>A MELA-AU 20 61511763 61511764 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant PH1848PY MELA-AU 20 61511764 61511764 single base substitution G A synonymous_variant P1848P 5544C>T MELA-AU 20 61511852 61511853 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant P1819F 5455CC>TT MELA-AU 20 61511891 61511891 single base substitution G A missense_variant P1806L 5417C>T MELA-AU 20 61512062 61512062 single base substitution G A missense_variant P1749L 5246C>T MELA-AU 20 61512090 61512090 single base substitution C T missense_variant G1740R 5218G>A MELA-AU 20 61512327 61512327 single base substitution G A missense_variant P1661S 4981C>T MELA-AU 20 61512521 61512521 single base substitution G A missense_variant S1596F 4787C>T MELA-AU 20 61512569 61512569 single base substitution C G missense_variant R1580T 4739G>C MELA-AU 20 61512576 61512576 single base substitution G A missense_variant L1578F 4732C>T MELA-AU 20 61512828 61512828 single base substitution C T missense_variant E1494K 4480G>A MELA-AU 20 61512886 61512886 single base substitution C T synonymous_variant E1474E 4422G>A MELA-AU 20 61513131 61513131 single base substitution G A missense_variant P1393S 4177C>T MELA-AU 20 61513942 61513942 single base substitution A G downstream_gene_variant MELA-AU 20 61513942 61513942 single base substitution A G intron_variant MELA-AU 20 61513956 61513957 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 20 61513956 61513957 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 20 61513971 61513971 single base substitution G A downstream_gene_variant MELA-AU 20 61513971 61513971 single base substitution G A intron_variant MELA-AU 20 61514576 61514576 single base substitution C T downstream_gene_variant MELA-AU 20 61514576 61514576 single base substitution C T intron_variant MELA-AU 20 61515243 61515243 single base substitution G A downstream_gene_variant MELA-AU 20 61515243 61515243 single base substitution G A intron_variant MELA-AU 20 61515542 61515542 single base substitution G A downstream_gene_variant MELA-AU 20 61515542 61515542 single base substitution G A intron_variant MELA-AU 20 61515978 61515978 single base substitution G A downstream_gene_variant MELA-AU 20 61515978 61515978 single base substitution G A intron_variant MELA-AU 20 61516021 61516021 single base substitution G A downstream_gene_variant MELA-AU 20 61516021 61516021 single base substitution G A intron_variant MELA-AU 20 61516379 61516379 single base substitution A G downstream_gene_variant MELA-AU 20 61516379 61516379 single base substitution A G intron_variant MELA-AU 20 61516566 61516566 single base substitution G A downstream_gene_variant MELA-AU 20 61516566 61516566 single base substitution G A intron_variant MELA-AU 20 61516827 61516827 single base substitution A G downstream_gene_variant MELA-AU 20 61516827 61516827 single base substitution A G intron_variant MELA-AU 20 61517271 61517271 single base substitution G A downstream_gene_variant MELA-AU 20 61517271 61517271 single base substitution G A intron_variant MELA-AU 20 61517449 61517449 single base substitution G A downstream_gene_variant MELA-AU 20 61517449 61517449 single base substitution G A intron_variant MELA-AU 20 61517526 61517526 single base substitution G A downstream_gene_variant MELA-AU 20 61517526 61517526 single base substitution G A intron_variant MELA-AU 20 61518297 61518298 multiple base substitution (>=2bp and <=200bp) GG AA downstream_gene_variant MELA-AU 20 61518297 61518298 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 20 61518298 61518299 multiple base substitution (>=2bp and <=200bp) GG AT downstream_gene_variant MELA-AU 20 61518298 61518299 multiple base substitution (>=2bp and <=200bp) GG AT intron_variant MELA-AU 20 61518445 61518445 single base substitution G A downstream_gene_variant MELA-AU 20 61518445 61518445 single base substitution G A intron_variant MELA-AU 20 61518983 61518983 single base substitution G A 3_prime_UTR_variant MELA-AU 20 61518983 61518983 single base substitution G A intron_variant MELA-AU 20 61518983 61518983 single base substitution G C 3_prime_UTR_variant MELA-AU 20 61518983 61518983 single base substitution G C intron_variant MELA-AU 20 61519690 61519690 single base substitution G A 3_prime_UTR_variant MELA-AU 20 61519690 61519690 single base substitution G A intron_variant MELA-AU 20 61520011 61520011 single base substitution C A 3_prime_UTR_variant MELA-AU 20 61520011 61520011 single base substitution C A intron_variant MELA-AU 20 61520064 61520065 multiple base substitution (>=2bp and <=200bp) CA AC 3_prime_UTR_variant MELA-AU 20 61520064 61520065 multiple base substitution (>=2bp and <=200bp) CA AC intron_variant MELA-AU 20 61520150 61520150 single base substitution G A 3_prime_UTR_variant MELA-AU 20 61520150 61520150 single base substitution G A intron_variant MELA-AU 20 61520606 61520606 single base substitution C G 3_prime_UTR_variant MELA-AU 20 61520606 61520606 single base substitution C G intron_variant MELA-AU 20 61520773 61520773 single base substitution C T 3_prime_UTR_variant MELA-AU 20 61520773 61520773 single base substitution C T intron_variant MELA-AU 20 61520780 61520780 single base substitution G A 3_prime_UTR_variant MELA-AU 20 61520780 61520780 single base substitution G A intron_variant MELA-AU 20 61521275 61521275 single base substitution C A 3_prime_UTR_variant MELA-AU 20 61521275 61521275 single base substitution C A intron_variant MELA-AU 20 61522554 61522554 single base substitution G T intron_variant MELA-AU 20 61522718 61522718 single base substitution G A intron_variant MELA-AU 20 61523903 61523903 single base substitution G C intron_variant MELA-AU 20 61525430 61525430 single base substitution C T missense_variant D897N 2689G>A MELA-AU 20 61525536 61525536 single base substitution G A synonymous_variant P861P 2583C>T MELA-AU 20 61525988 61525988 single base substitution G A intron_variant MELA-AU 20 61526274 61526274 single base substitution G A splice_region_variant MELA-AU 20 61526463 61526463 single base substitution G A synonymous_variant L757L 2269C>T MELA-AU 20 61527765 61527765 single base substitution G A intron_variant MELA-AU 20 61527855 61527855 single base substitution G A intron_variant MELA-AU 20 61527972 61527972 single base substitution G A synonymous_variant R655R 1965C>T MELA-AU 20 61528090 61528091 multiple base substitution (>=2bp and <=200bp) GG AA missense_variant P616L 1846CC>TT MELA-AU 20 61528142 61528142 single base substitution A C missense_variant W599G 1795T>G MELA-AU 20 61528239 61528239 single base substitution G A synonymous_variant L566L 1698C>T MELA-AU 20 61528326 61528326 single base substitution G C synonymous_variant S537S 1611C>G MELA-AU 20 61528518 61528519 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 20 61528720 61528720 single base substitution G A intron_variant MELA-AU 20 61529220 61529220 single base substitution C T intron_variant MELA-AU 20 61529652 61529652 single base substitution G A intron_variant MELA-AU 20 61530866 61530866 single base substitution G A intron_variant MELA-AU 20 61531584 61531584 single base substitution C T downstream_gene_variant MELA-AU 20 61531584 61531584 single base substitution C T intron_variant MELA-AU 20 61535024 61535024 single base substitution G A downstream_gene_variant MELA-AU 20 61535024 61535024 single base substitution G A intron_variant MELA-AU 20 61535952 61535952 single base substitution G A downstream_gene_variant MELA-AU 20 61535952 61535952 single base substitution G A intron_variant MELA-AU 20 61536109 61536109 single base substitution G A downstream_gene_variant MELA-AU 20 61536109 61536109 single base substitution G A intron_variant MELA-AU 20 61536493 61536493 single base substitution C T 3_prime_UTR_variant MELA-AU 20 61536493 61536493 single base substitution C T downstream_gene_variant MELA-AU 20 61536493 61536493 single base substitution C T intron_variant MELA-AU 20 61536514 61536514 single base substitution G A 3_prime_UTR_variant MELA-AU 20 61536514 61536514 single base substitution G A downstream_gene_variant MELA-AU 20 61536514 61536514 single base substitution G A intron_variant MELA-AU 20 61537539 61537539 single base substitution C T intron_variant MELA-AU 20 61537649 61537649 single base substitution C T intron_variant MELA-AU 20 61537719 61537719 single base substitution T C intron_variant MELA-AU 20 61537838 61537838 single base substitution G A intron_variant MELA-AU 20 61537868 61537868 single base substitution G A intron_variant MELA-AU 20 61538341 61538341 single base substitution A G intron_variant MELA-AU 20 61539069 61539069 single base substitution A G intron_variant MELA-AU 20 61539174 61539174 single base substitution G A intron_variant MELA-AU 20 61539409 61539409 single base substitution G A intron_variant MELA-AU 20 61539435 61539435 single base substitution G A intron_variant MELA-AU 20 61539553 61539553 single base substitution G A intron_variant MELA-AU 20 61539677 61539677 single base substitution G A intron_variant MELA-AU 20 61539835 61539835 single base substitution G A intron_variant MELA-AU 20 61540138 61540138 single base substitution G A intron_variant MELA-AU 20 61540830 61540830 single base substitution G A intron_variant MELA-AU 20 61540834 61540834 single base substitution G A intron_variant MELA-AU 20 61540880 61540880 single base substitution G A intron_variant MELA-AU 20 61541821 61541821 single base substitution G A intron_variant MELA-AU 20 61542081 61542081 single base substitution T C intron_variant MELA-AU 20 61542653 61542653 deletion of <=200bp G - frameshift_variant A104 MELA-AU 20 61543301 61543301 single base substitution G A intron_variant MELA-AU 20 61543802 61543802 single base substitution G A intron_variant MELA-AU 20 61544398 61544398 single base substitution G A intron_variant MELA-AU 20 61544684 61544684 single base substitution G A intron_variant MELA-AU 20 61545015 61545015 single base substitution G A intron_variant MELA-AU 20 61545043 61545043 single base substitution G A intron_variant MELA-AU 20 61545744 61545745 multiple base substitution (>=2bp and <=200bp) CC TT 5_prime_UTR_variant MELA-AU 20 61545964 61545964 single base substitution G A intron_variant MELA-AU 20 61545964 61545964 single base substitution G A upstream_gene_variant MELA-AU 20 61546088 61546088 single base substitution G A intron_variant MELA-AU 20 61546088 61546088 single base substitution G A upstream_gene_variant MELA-AU 20 61547013 61547013 single base substitution G A intron_variant MELA-AU 20 61547013 61547013 single base substitution G A upstream_gene_variant MELA-AU 20 61547932 61547932 single base substitution C T intron_variant MELA-AU 20 61547932 61547932 single base substitution C T upstream_gene_variant MELA-AU 20 61547954 61547954 single base substitution G A intron_variant MELA-AU 20 61547954 61547954 single base substitution G A upstream_gene_variant MELA-AU 20 61548366 61548366 single base substitution G A intron_variant MELA-AU 20 61548366 61548366 single base substitution G A upstream_gene_variant MELA-AU 20 61548913 61548913 single base substitution G A intron_variant MELA-AU 20 61548913 61548913 single base substitution G A upstream_gene_variant MELA-AU 20 61549101 61549101 single base substitution G A intron_variant MELA-AU 20 61549101 61549101 single base substitution G A upstream_gene_variant MELA-AU 20 61549133 61549134 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 20 61549133 61549134 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 20 61549257 61549257 single base substitution C A intron_variant MELA-AU 20 61549257 61549257 single base substitution C A upstream_gene_variant MELA-AU 20 61549912 61549912 single base substitution G A intron_variant MELA-AU 20 61549912 61549912 single base substitution G A upstream_gene_variant MELA-AU 20 61550158 61550158 single base substitution C T intron_variant MELA-AU 20 61550158 61550158 single base substitution C T upstream_gene_variant MELA-AU 20 61551101 61551101 single base substitution G A intron_variant MELA-AU 20 61551927 61551927 single base substitution C G intron_variant MELA-AU 20 61551942 61551942 single base substitution C T intron_variant MELA-AU 20 61552761 61552761 single base substitution T C intron_variant MELA-AU 20 61552912 61552912 single base substitution G A intron_variant MELA-AU 20 61552938 61552938 single base substitution A G intron_variant MELA-AU 20 61553583 61553583 single base substitution C T intron_variant MELA-AU 20 61554194 61554194 single base substitution C T intron_variant MELA-AU 20 61554399 61554399 single base substitution G A intron_variant MELA-AU 20 61554519 61554519 single base substitution C T intron_variant MELA-AU 20 61555062 61555062 single base substitution A G intron_variant MELA-AU 20 61555111 61555111 single base substitution T C intron_variant MELA-AU 20 61556324 61556324 single base substitution C T intron_variant MELA-AU 20 61558711 61558711 single base substitution C T intron_variant MELA-AU 20 61558711 61558711 single base substitution C T upstream_gene_variant MELA-AU 20 61558812 61558812 single base substitution G A intron_variant MELA-AU 20 61558812 61558812 single base substitution G A upstream_gene_variant MELA-AU 20 61559048 61559048 single base substitution G A intron_variant MELA-AU 20 61559048 61559048 single base substitution G A upstream_gene_variant MELA-AU 20 61559436 61559436 single base substitution G A intron_variant MELA-AU 20 61559436 61559436 single base substitution G A upstream_gene_variant MELA-AU 20 61559506 61559506 single base substitution G A intron_variant MELA-AU 20 61559506 61559506 single base substitution G A upstream_gene_variant MELA-AU 20 61559850 61559850 single base substitution G A intron_variant MELA-AU 20 61559850 61559850 single base substitution G A upstream_gene_variant MELA-AU 20 61559937 61559937 single base substitution C T intron_variant MELA-AU 20 61559937 61559937 single base substitution C T upstream_gene_variant MELA-AU 20 61560016 61560016 single base substitution G A intron_variant MELA-AU 20 61560016 61560016 single base substitution G A upstream_gene_variant MELA-AU 20 61561046 61561046 single base substitution T C intron_variant MELA-AU 20 61561046 61561046 single base substitution T C upstream_gene_variant MELA-AU 20 61561048 61561049 deletion of <=200bp TA - intron_variant MELA-AU 20 61561048 61561049 deletion of <=200bp TA - upstream_gene_variant MELA-AU 20 61561349 61561349 single base substitution C T intron_variant MELA-AU 20 61561349 61561349 single base substitution C T upstream_gene_variant MELA-AU 20 61561871 61561871 single base substitution G A intron_variant MELA-AU 20 61561871 61561871 single base substitution G A upstream_gene_variant MELA-AU 20 61562766 61562766 single base substitution T C intron_variant MELA-AU 20 61562766 61562766 single base substitution T C upstream_gene_variant MELA-AU 20 61562866 61562866 deletion of <=200bp A - intron_variant MELA-AU 20 61563443 61563443 single base substitution C G intron_variant MELA-AU 20 61563807 61563807 single base substitution A T intron_variant MELA-AU 20 61564163 61564163 single base substitution G A intron_variant MELA-AU 20 61564409 61564409 single base substitution A G intron_variant MELA-AU 20 61564985 61564985 single base substitution G A intron_variant MELA-AU 20 61565566 61565566 single base substitution G A intron_variant MELA-AU 20 61566477 61566477 single base substitution G A intron_variant MELA-AU 20 61566949 61566949 single base substitution C T intron_variant MELA-AU 20 61567585 61567585 single base substitution C T intron_variant MELA-AU 20 61568818 61568818 single base substitution C G intron_variant MELA-AU 20 61568934 61568934 single base substitution G A intron_variant MELA-AU 20 61569306 61569306 single base substitution G A upstream_gene_variant MELA-AU 20 61569326 61569326 single base substitution C T upstream_gene_variant MELA-AU 20 61569458 61569458 single base substitution C G upstream_gene_variant MELA-AU 20 61570380 61570380 single base substitution G A upstream_gene_variant MELA-AU 20 61570965 61570965 single base substitution G A upstream_gene_variant MELA-AU 20 61571391 61571391 single base substitution C T upstream_gene_variant MELA-AU 20 61572758 61572758 single base substitution T C upstream_gene_variant MELA-AU 20 61572760 61572760 single base substitution C T upstream_gene_variant MELA-AU 20 61573266 61573266 single base substitution G A upstream_gene_variant MELA-AU 20 61574297 61574297 single base substitution C T upstream_gene_variant ORCA-IN 20 61505107 61505107 single base substitution C G downstream_gene_variant ORCA-IN 20 61507842 61507842 single base substitution G T downstream_gene_variant ORCA-IN 20 61511011 61511011 single base substitution C A synonymous_variant P2099P 6297G>T ORCA-IN 20 61511498 61511498 single base substitution G T missense_variant A1937D 5810C>A ORCA-IN 20 61513864 61513864 single base substitution T C downstream_gene_variant ORCA-IN 20 61513864 61513864 single base substitution T C intron_variant ORCA-IN 20 61530307 61530307 single base substitution C G intron_variant ORCA-IN 20 61536233 61536233 single base substitution C A downstream_gene_variant ORCA-IN 20 61536233 61536233 single base substitution C A intron_variant ORCA-IN 20 61542191 61542191 single base substitution C A missense_variant K258N 774G>T ORCA-IN 20 61545708 61545708 single base substitution G A 5_prime_UTR_premature_start_codon_gain_variant OV-AU 20 61505320 61505320 single base substitution C T downstream_gene_variant OV-AU 20 61507675 61507675 single base substitution G T downstream_gene_variant OV-AU 20 61512007 61512007 single base substitution G A synonymous_variant H1767H 5301C>T OV-AU 20 61514484 61514484 single base substitution C A downstream_gene_variant OV-AU 20 61514484 61514484 single base substitution C A intron_variant OV-AU 20 61519594 61519594 single base substitution T C 3_prime_UTR_variant OV-AU 20 61519594 61519594 single base substitution T C intron_variant OV-AU 20 61520402 61520402 single base substitution G A 3_prime_UTR_variant OV-AU 20 61520402 61520402 single base substitution G A intron_variant OV-AU 20 61520635 61520635 single base substitution C T 3_prime_UTR_variant OV-AU 20 61520635 61520635 single base substitution C T intron_variant OV-AU 20 61526810 61526810 single base substitution C A intron_variant OV-AU 20 61530232 61530232 single base substitution C T intron_variant OV-AU 20 61531183 61531183 single base substitution C G intron_variant OV-AU 20 61531428 61531428 single base substitution G T downstream_gene_variant OV-AU 20 61531428 61531428 single base substitution G T intron_variant OV-AU 20 61536192 61536192 single base substitution A G downstream_gene_variant OV-AU 20 61536192 61536192 single base substitution A G intron_variant OV-AU 20 61542848 61542848 single base substitution G A synonymous_variant G39G 117C>T OV-AU 20 61548274 61548274 single base substitution C T intron_variant OV-AU 20 61548274 61548274 single base substitution C T upstream_gene_variant OV-AU 20 61556202 61556202 single base substitution C T intron_variant OV-AU 20 61560135 61560135 single base substitution G C intron_variant OV-AU 20 61560135 61560135 single base substitution G C upstream_gene_variant OV-AU 20 61568027 61568027 single base substitution C T intron_variant OV-US 20 61527958 61527958 single base substitution C T missense_variant S660N 1979G>A OV-US 20 61538627 61538627 single base substitution C T missense_variant D416N 1246G>A PACA-AU 20 61510761 61510761 single base substitution G A stop_gained R2183* 6547C>T PACA-AU 20 61510822 61510822 single base substitution C T synonymous_variant E2162E 6486G>A PACA-AU 20 61511711 61511711 single base substitution G A missense_variant A1866V 5597C>T PACA-AU 20 61512562 61512562 single base substitution C T synonymous_variant S1582S 4746G>A PACA-AU 20 61517096 61517096 single base substitution T C downstream_gene_variant PACA-AU 20 61517096 61517096 single base substitution T C intron_variant PACA-AU 20 61518023 61518023 single base substitution C T downstream_gene_variant PACA-AU 20 61518023 61518023 single base substitution C T intron_variant PACA-AU 20 61519124 61519124 single base substitution C T 3_prime_UTR_variant PACA-AU 20 61519124 61519124 single base substitution C T intron_variant PACA-AU 20 61520738 61520744 deletion of <=200bp AGCTCCA - 3_prime_UTR_variant PACA-AU 20 61520738 61520744 deletion of <=200bp AGCTCCA - intron_variant PACA-AU 20 61520775 61520775 single base substitution A T 3_prime_UTR_variant PACA-AU 20 61520775 61520775 single base substitution A T intron_variant PACA-AU 20 61522357 61522357 single base substitution C T missense_variant A1166T 3496G>A PACA-AU 20 61523102 61523102 single base substitution C T intron_variant PACA-AU 20 61523398 61523398 single base substitution T A missense_variant R1096W 3286A>T PACA-AU 20 61526538 61526538 single base substitution T C intron_variant PACA-AU 20 61528153 61528153 single base substitution G C missense_variant P595R 1784C>G PACA-AU 20 61532096 61532096 single base substitution T C downstream_gene_variant PACA-AU 20 61532096 61532096 single base substitution T C intron_variant PACA-AU 20 61532598 61532598 single base substitution T G downstream_gene_variant PACA-AU 20 61532598 61532598 single base substitution T G intron_variant PACA-AU 20 61536246 61536246 single base substitution G C downstream_gene_variant PACA-AU 20 61536246 61536246 single base substitution G C intron_variant PACA-AU 20 61537505 61537505 single base substitution C A intron_variant PACA-AU 20 61541881 61541881 deletion of <=200bp G - intron_variant PACA-AU 20 61542465 61542465 single base substitution C T missense_variant R167H 500G>A PACA-AU 20 61542521 61542521 single base substitution G A synonymous_variant H148H 444C>T PACA-AU 20 61545591 61545591 single base substitution T C 5_prime_UTR_variant PACA-AU 20 61552606 61552606 deletion of <=200bp A - intron_variant PACA-AU 20 61562927 61562927 single base substitution G A intron_variant PACA-AU 20 61563088 61563088 single base substitution G A intron_variant PACA-AU 20 61566563 61566563 single base substitution T A intron_variant PACA-AU 20 61570815 61570815 single base substitution T G upstream_gene_variant PACA-AU 20 61573940 61573940 single base substitution A G upstream_gene_variant PACA-CA 20 61505954 61505954 single base substitution T C downstream_gene_variant PACA-CA 20 61508830 61508830 single base substitution G A downstream_gene_variant PACA-CA 20 61510103 61510103 single base substitution T C 3_prime_UTR_variant PACA-CA 20 61510819 61510819 single base substitution G A synonymous_variant A2163A 6489C>T PACA-CA 20 61513772 61513775 deletion of <=200bp AAAC - downstream_gene_variant PACA-CA 20 61513772 61513775 deletion of <=200bp AAAC - intron_variant PACA-CA 20 61514164 61514164 single base substitution G A downstream_gene_variant PACA-CA 20 61514164 61514164 single base substitution G A intron_variant PACA-CA 20 61519623 61519623 single base substitution G A 3_prime_UTR_variant PACA-CA 20 61519623 61519623 single base substitution G A intron_variant PACA-CA 20 61522619 61522619 single base substitution G A intron_variant PACA-CA 20 61525472 61525472 single base substitution A G synonymous_variant L883L 2647T>C PACA-CA 20 61527274 61527274 single base substitution T A intron_variant PACA-CA 20 61527357 61527367 deletion of <=200bp GGGAAGCCAGG - intron_variant PACA-CA 20 61527732 61527732 single base substitution G A synonymous_variant S689S 2067C>T PACA-CA 20 61532018 61532018 single base substitution T A downstream_gene_variant PACA-CA 20 61532018 61532018 single base substitution T A intron_variant PACA-CA 20 61537518 61537518 single base substitution T A intron_variant PACA-CA 20 61537531 61537531 single base substitution C T intron_variant PACA-CA 20 61540189 61540189 single base substitution C A intron_variant PACA-CA 20 61543172 61543194 deletion of <=200bp CTAACGTTTAGACAAAAATACAG - intron_variant PACA-CA 20 61544028 61544028 single base substitution C G intron_variant PACA-CA 20 61545107 61545107 single base substitution A G intron_variant PACA-CA 20 61546907 61546907 single base substitution C A intron_variant PACA-CA 20 61546907 61546907 single base substitution C A upstream_gene_variant PACA-CA 20 61552411 61552411 insertion of <=200bp - T intron_variant PACA-CA 20 61553463 61553463 single base substitution C T intron_variant PACA-CA 20 61561524 61561524 single base substitution T A intron_variant PACA-CA 20 61561524 61561524 single base substitution T A upstream_gene_variant PACA-CA 20 61561574 61561574 single base substitution A C intron_variant PACA-CA 20 61561574 61561574 single base substitution A C upstream_gene_variant PACA-CA 20 61562120 61562120 single base substitution G A intron_variant PACA-CA 20 61562120 61562120 single base substitution G A upstream_gene_variant PACA-CA 20 61563582 61563582 single base substitution C T intron_variant PACA-CA 20 61569272 61569272 single base substitution G T 5_prime_UTR_variant PACA-CA 20 61570908 61570908 single base substitution C T upstream_gene_variant PAEN-AU 20 61526311 61526311 single base substitution G A intron_variant PAEN-AU 20 61535633 61535633 single base substitution G T downstream_gene_variant PAEN-AU 20 61535633 61535633 single base substitution G T intron_variant PBCA-DE 20 61510578 61510578 single base substitution G A 3_prime_UTR_variant PBCA-DE 20 61512109 61512109 single base substitution G A synonymous_variant T1733T 5199C>T PBCA-DE 20 61515134 61515134 single base substitution C T downstream_gene_variant PBCA-DE 20 61515134 61515134 single base substitution C T intron_variant PBCA-DE 20 61519589 61519589 insertion of <=200bp - TG 3_prime_UTR_variant PBCA-DE 20 61519589 61519589 insertion of <=200bp - TG intron_variant PBCA-DE 20 61522426 61522426 single base substitution G A missense_variant R1143C 3427C>T PBCA-DE 20 61525916 61525916 insertion of <=200bp - A intron_variant PBCA-DE 20 61534137 61534137 single base substitution C T downstream_gene_variant PBCA-DE 20 61534137 61534137 single base substitution C T intron_variant PBCA-DE 20 61547728 61547728 single base substitution C T intron_variant PBCA-DE 20 61547728 61547728 single base substitution C T upstream_gene_variant PBCA-DE 20 61560321 61560321 deletion of <=200bp A - intron_variant PBCA-DE 20 61560321 61560321 deletion of <=200bp A - upstream_gene_variant PBCA-DE 20 61561048 61561049 deletion of <=200bp TA - intron_variant PBCA-DE 20 61561048 61561049 deletion of <=200bp TA - upstream_gene_variant PBCA-DE 20 61567611 61567616 deletion of <=200bp AAAAAT - intron_variant PRAD-CA 20 61504376 61504376 single base substitution G A downstream_gene_variant PRAD-CA 20 61527862 61527862 single base substitution A G intron_variant PRAD-CA 20 61538699 61538699 single base substitution G A missense_variant P392S 1174C>T PRAD-CA 20 61541654 61541654 single base substitution G C intron_variant PRAD-CA 20 61553595 61553595 single base substitution T C intron_variant PRAD-CA 20 61554238 61554238 single base substitution A T intron_variant PRAD-CA 20 61556254 61556254 single base substitution C T intron_variant PRAD-CA 20 61561574 61561574 single base substitution A C intron_variant PRAD-CA 20 61561574 61561574 single base substitution A C upstream_gene_variant PRAD-CA 20 61568198 61568198 single base substitution A G intron_variant PRAD-CA 20 61569348 61569348 single base substitution C A upstream_gene_variant PRAD-UK 20 61507778 61507778 single base substitution T G downstream_gene_variant PRAD-UK 20 61534759 61534759 single base substitution C T downstream_gene_variant PRAD-UK 20 61534759 61534759 single base substitution C T intron_variant PRAD-UK 20 61537661 61537661 single base substitution A T intron_variant PRAD-UK 20 61541679 61541679 single base substitution C T intron_variant PRAD-UK 20 61546230 61546245 deletion of <=200bp AATTAAAAACAAGAAA - intron_variant PRAD-UK 20 61546230 61546245 deletion of <=200bp AATTAAAAACAAGAAA - upstream_gene_variant PRAD-UK 20 61553248 61553258 multiple base substitution (>=2bp and <=200bp) TATATATCCAC TGTCCAA intron_variant PRAD-UK 20 61555599 61555599 single base substitution G A intron_variant PRAD-UK 20 61562591 61562601 deletion of <=200bp CTGCAGTATTT - intron_variant PRAD-UK 20 61562591 61562601 deletion of <=200bp CTGCAGTATTT - upstream_gene_variant PRAD-UK 20 61569798 61569798 single base substitution G T upstream_gene_variant PRAD-US 20 61510982 61510982 single base substitution G A missense_variant A2109V 6326C>T PRAD-US 20 61513601 61513601 single base substitution T C downstream_gene_variant PRAD-US 20 61513601 61513601 single base substitution T C missense_variant Q1236R 3707A>G PRAD-US 20 61513671 61513671 single base substitution C T downstream_gene_variant PRAD-US 20 61513671 61513671 single base substitution C T missense_variant E1213K 3637G>A PRAD-US 20 61525227 61525227 single base substitution G A synonymous_variant S964S 2892C>T PRAD-US 20 61525242 61525242 single base substitution G A synonymous_variant T959T 2877C>T READ-US 20 61511868 61511868 single base substitution G A stop_gained Q1814* 5440C>T READ-US 20 61513394 61513394 single base substitution G A missense_variant S1305L 3914C>T READ-US 20 61527926 61527926 single base substitution G A missense_variant R671W 2011C>T READ-US 20 61542301 61542301 single base substitution C T missense_variant D222N 664G>A READ-US 20 61572956 61572956 single base substitution G T upstream_gene_variant RECA-EU 20 61504994 61504994 single base substitution C T downstream_gene_variant RECA-EU 20 61506257 61506257 single base substitution G C downstream_gene_variant RECA-EU 20 61509683 61509683 single base substitution G A 3_prime_UTR_variant RECA-EU 20 61517391 61517391 single base substitution A G downstream_gene_variant RECA-EU 20 61517391 61517391 single base substitution A G intron_variant RECA-EU 20 61524637 61524637 single base substitution G A intron_variant RECA-EU 20 61532537 61532537 single base substitution G T downstream_gene_variant RECA-EU 20 61532537 61532537 single base substitution G T intron_variant RECA-EU 20 61534159 61534159 single base substitution G A downstream_gene_variant RECA-EU 20 61534159 61534159 single base substitution G A intron_variant RECA-EU 20 61539830 61539830 single base substitution A C intron_variant RECA-EU 20 61553294 61553294 single base substitution A G intron_variant RECA-EU 20 61553543 61553543 single base substitution T C intron_variant RECA-EU 20 61554808 61554808 single base substitution G T intron_variant RECA-EU 20 61556441 61556441 single base substitution A C intron_variant RECA-EU 20 61572829 61572829 single base substitution T C upstream_gene_variant SKCA-BR 20 61507362 61507364 deletion of <=200bp CCT - downstream_gene_variant SKCA-BR 20 61509090 61509090 single base substitution G A 3_prime_UTR_variant SKCA-BR 20 61509090 61509090 single base substitution G A downstream_gene_variant SKCA-BR 20 61513454 61513454 single base substitution C G missense_variant S1285T 3854G>C SKCA-BR 20 61513749 61513749 single base substitution G A downstream_gene_variant SKCA-BR 20 61513749 61513749 single base substitution G A missense_variant P1187S 3559C>T SKCA-BR 20 61514251 61514251 single base substitution G A downstream_gene_variant SKCA-BR 20 61514251 61514251 single base substitution G A intron_variant SKCA-BR 20 61514291 61514291 single base substitution T C downstream_gene_variant SKCA-BR 20 61514291 61514291 single base substitution T C intron_variant SKCA-BR 20 61517012 61517012 single base substitution T C downstream_gene_variant SKCA-BR 20 61517012 61517012 single base substitution T C intron_variant SKCA-BR 20 61527541 61527541 single base substitution G A intron_variant SKCA-BR 20 61528197 61528197 single base substitution T G synonymous_variant T580T 1740A>C SKCA-BR 20 61533052 61533052 single base substitution G A downstream_gene_variant SKCA-BR 20 61533052 61533052 single base substitution G A intron_variant SKCA-BR 20 61537456 61537456 single base substitution G A intron_variant SKCA-BR 20 61537456 61537456 single base substitution G A splice_region_variant SKCA-BR 20 61543236 61543236 single base substitution G A intron_variant SKCA-BR 20 61543753 61543753 single base substitution G A intron_variant SKCA-BR 20 61544398 61544398 single base substitution G A intron_variant SKCA-BR 20 61550012 61550012 single base substitution G A intron_variant SKCA-BR 20 61550012 61550012 single base substitution G A upstream_gene_variant SKCA-BR 20 61553386 61553386 single base substitution G A intron_variant SKCA-BR 20 61553548 61553548 single base substitution G A intron_variant SKCA-BR 20 61553563 61553563 insertion of <=200bp - CATAT intron_variant SKCA-BR 20 61553565 61553583 deletion of <=200bp TATATATACACACACACAC - intron_variant SKCA-BR 20 61557782 61557789 deletion of <=200bp ACCGCAGG - intron_variant SKCA-BR 20 61557782 61557789 deletion of <=200bp ACCGCAGG - splice_donor_variant SKCA-BR 20 61562931 61562931 single base substitution T G intron_variant SKCA-BR 20 61567544 61567544 single base substitution G A intron_variant SKCA-BR 20 61569285 61569285 single base substitution G A 5_prime_UTR_variant SKCA-BR 20 61569285 61569285 single base substitution G A upstream_gene_variant SKCA-BR 20 61569286 61569286 single base substitution G A 5_prime_UTR_variant SKCA-BR 20 61569286 61569286 single base substitution G A upstream_gene_variant SKCA-BR 20 61569306 61569306 single base substitution G A upstream_gene_variant SKCA-BR 20 61569461 61569461 single base substitution G C upstream_gene_variant SKCA-BR 20 61569981 61569981 single base substitution G A upstream_gene_variant SKCA-BR 20 61571539 61571539 insertion of <=200bp - CT upstream_gene_variant SKCA-BR 20 61571721 61571721 single base substitution A G upstream_gene_variant SKCM-US 20 61510880 61510880 single base substitution G A missense_variant S2143F 6428C>T SKCM-US 20 61510928 61510928 single base substitution C T missense_variant R2127Q 6380G>A SKCM-US 20 61510970 61510970 single base substitution C T missense_variant R2113K 6338G>A SKCM-US 20 61511017 61511017 single base substitution C T synonymous_variant E2097E 6291G>A SKCM-US 20 61511132 61511132 single base substitution G A missense_variant P2059L 6176C>T SKCM-US 20 61511156 61511156 single base substitution G A missense_variant S2051F 6152C>T SKCM-US 20 61511288 61511288 single base substitution G A missense_variant S2007L 6020C>T SKCM-US 20 61511312 61511312 single base substitution G A missense_variant S1999F 5996C>T SKCM-US 20 61511407 61511407 single base substitution G A synonymous_variant F1967F 5901C>T SKCM-US 20 61511438 61511438 single base substitution G A missense_variant P1957L 5870C>T SKCM-US 20 61511439 61511439 single base substitution G A missense_variant P1957S 5869C>T SKCM-US 20 61511484 61511484 single base substitution G A missense_variant P1942S 5824C>T SKCM-US 20 61511764 61511764 single base substitution G A synonymous_variant P1848P 5544C>T SKCM-US 20 61511765 61511765 single base substitution G A missense_variant P1848L 5543C>T SKCM-US 20 61511906 61511906 single base substitution C T missense_variant G1801E 5402G>A SKCM-US 20 61511949 61511949 single base substitution C T missense_variant A1787T 5359G>A SKCM-US 20 61511969 61511969 single base substitution G A missense_variant P1780L 5339C>T SKCM-US 20 61511969 61511969 single base substitution G C missense_variant P1780R 5339C>G SKCM-US 20 61511988 61511988 single base substitution G A missense_variant P1774S 5320C>T SKCM-US 20 61512000 61512000 single base substitution T C missense_variant N1770D 5308A>G SKCM-US 20 61512276 61512276 single base substitution C T missense_variant G1678S 5032G>A SKCM-US 20 61512325 61512325 single base substitution G A synonymous_variant P1661P 4983C>T SKCM-US 20 61512356 61512356 single base substitution G A missense_variant S1651L 4952C>T SKCM-US 20 61512461 61512461 single base substitution G A missense_variant S1616F 4847C>T SKCM-US 20 61512521 61512521 single base substitution G A missense_variant S1596F 4787C>T SKCM-US 20 61512857 61512857 single base substitution T G missense_variant K1484T 4451A>C SKCM-US 20 61512940 61512940 single base substitution G A synonymous_variant S1456S 4368C>T SKCM-US 20 61513160 61513160 single base substitution C T missense_variant R1383K 4148G>A SKCM-US 20 61513219 61513219 single base substitution G A synonymous_variant I1363I 4089C>T SKCM-US 20 61513264 61513264 single base substitution G A synonymous_variant T1348T 4044C>T SKCM-US 20 61513284 61513284 single base substitution G A missense_variant L1342F 4024C>T SKCM-US 20 61513394 61513394 single base substitution G A missense_variant S1305L 3914C>T SKCM-US 20 61513451 61513451 single base substitution G A missense_variant P1286L 3857C>T SKCM-US 20 61513506 61513506 single base substitution G A missense_variant P1268S 3802C>T SKCM-US 20 61513517 61513517 single base substitution G A missense_variant P1264L 3791C>T SKCM-US 20 61513529 61513529 single base substitution G A missense_variant S1260L 3779C>T SKCM-US 20 61524251 61524251 single base substitution G A synonymous_variant T1055T 3165C>T SKCM-US 20 61525205 61525205 single base substitution G A missense_variant P972S 2914C>T SKCM-US 20 61525227 61525227 single base substitution G A synonymous_variant S964S 2892C>T SKCM-US 20 61525396 61525396 single base substitution G A missense_variant P908L 2723C>T SKCM-US 20 61525489 61525489 single base substitution G A missense_variant S877F 2630C>T SKCM-US 20 61525538 61525538 single base substitution G A missense_variant P861S 2581C>T SKCM-US 20 61526218 61526218 single base substitution G A missense_variant P794S 2380C>T SKCM-US 20 61527623 61527623 single base substitution G A missense_variant R726C 2176C>T SKCM-US 20 61528027 61528027 single base substitution G A missense_variant A637V 1910C>T SKCM-US 20 61528167 61528167 single base substitution G A synonymous_variant F590F 1770C>T SKCM-US 20 61528235 61528235 single base substitution G A missense_variant P568S 1702C>T SKCM-US 20 61528272 61528272 single base substitution G A synonymous_variant S555S 1665C>T SKCM-US 20 61528327 61528327 single base substitution G A missense_variant S537F 1610C>T SKCM-US 20 61537257 61537257 single base substitution G A missense_variant P524S 1570C>T SKCM-US 20 61537302 61537302 single base substitution G A missense_variant H509Y 1525C>T SKCM-US 20 61538515 61538515 single base substitution G A missense_variant P453L 1358C>T SKCM-US 20 61542308 61542308 single base substitution G A synonymous_variant P219P 657C>T SKCM-US 20 61542327 61542327 single base substitution A G missense_variant L213P 638T>C SKCM-US 20 61542375 61542375 single base substitution G A missense_variant P197L 590C>T SKCM-US 20 61542407 61542407 single base substitution A G synonymous_variant S186S 558T>C SKCM-US 20 61542525 61542525 single base substitution T C missense_variant D147G 440A>G SKCM-US 20 61542877 61542877 single base substitution G A stop_gained R30* 88C>T SKCM-US 20 61572944 61572944 single base substitution C T upstream_gene_variant STAD-US 20 61510982 61510982 single base substitution G A missense_variant A2109V 6326C>T STAD-US 20 61511012 61511012 single base substitution G T missense_variant P2099Q 6296C>A STAD-US 20 61511147 61511147 single base substitution G A missense_variant A2054V 6161C>T STAD-US 20 61511207 61511207 deletion of <=200bp G - frameshift_variant P2034 STAD-US 20 61512061 61512061 single base substitution C T synonymous_variant P1749P 5247G>A STAD-US 20 61512074 61512074 deletion of <=200bp C - frameshift_variant G1745 STAD-US 20 61512442 61512442 single base substitution G A synonymous_variant G1622G 4866C>T STAD-US 20 61512527 61512528 deletion of <=200bp TC - frameshift_variant D1594 STAD-US 20 61512623 61512623 single base substitution T A missense_variant Q1562L 4685A>T STAD-US 20 61512757 61512757 single base substitution C A synonymous_variant S1517S 4551G>T STAD-US 20 61512787 61512787 single base substitution G A synonymous_variant V1507V 4521C>T STAD-US 20 61512859 61512859 single base substitution G A synonymous_variant N1483N 4449C>T STAD-US 20 61512878 61512878 single base substitution T G missense_variant K1477T 4430A>C STAD-US 20 61512957 61512957 single base substitution C A missense_variant D1451Y 4351G>T STAD-US 20 61512983 61512983 single base substitution T A missense_variant D1442V 4325A>T STAD-US 20 61513050 61513050 single base substitution C T missense_variant E1420K 4258G>A STAD-US 20 61513091 61513091 single base substitution C T missense_variant R1406Q 4217G>A STAD-US 20 61513128 61513128 single base substitution C T missense_variant E1394K 4180G>A STAD-US 20 61513394 61513394 single base substitution G A missense_variant S1305L 3914C>T STAD-US 20 61513397 61513397 single base substitution G A missense_variant A1304V 3911C>T STAD-US 20 61513486 61513486 insertion of <=200bp - T frameshift_variant K1274K? STAD-US 20 61513523 61513523 single base substitution G A missense_variant P1262L 3785C>T STAD-US 20 61513747 61513747 single base substitution C T downstream_gene_variant STAD-US 20 61513747 61513747 single base substitution C T synonymous_variant P1187P 3561G>A STAD-US 20 61525226 61525226 single base substitution C A missense_variant G965C 2893G>T STAD-US 20 61525797 61525797 single base substitution T C missense_variant H847R 2540A>G STAD-US 20 61525801 61525801 single base substitution C A missense_variant A846S 2536G>T STAD-US 20 61525803 61525803 single base substitution C T missense_variant R845H 2534G>A STAD-US 20 61526496 61526496 single base substitution G A missense_variant R746C 2236C>T STAD-US 20 61528048 61528048 single base substitution C T missense_variant G630D 1889G>A STAD-US 20 61528133 61528133 single base substitution C T missense_variant A602T 1804G>A STAD-US 20 61537350 61537350 single base substitution C T missense_variant G493R 1477G>A STAD-US 20 61541269 61541269 single base substitution T C missense_variant I315V 943A>G STAD-US 20 61541334 61541334 single base substitution T C missense_variant H293R 878A>G STAD-US 20 61542173 61542173 single base substitution G A synonymous_variant Y264Y 792C>T STAD-US 20 61542343 61542343 single base substitution T C missense_variant T208A 622A>G STAD-US 20 61542508 61542508 single base substitution C T missense_variant D153N 457G>A STAD-US 20 61542717 61542717 single base substitution C T missense_variant R83H 248G>A STAD-US 20 61542719 61542719 single base substitution C T synonymous_variant R82R 246G>A STAD-US 20 61542746 61542746 single base substitution G A synonymous_variant R73R 219C>T THCA-SA 20 61509380 61509380 single base substitution A C 3_prime_UTR_variant THCA-SA 20 61512185 61512185 single base substitution G C missense_variant S1708C 5123C>G THCA-SA 20 61512380 61512380 insertion of <=200bp - G frameshift_variant R1643R? THCA-SA 20 61520016 61520016 single base substitution A G 3_prime_UTR_variant THCA-SA 20 61520016 61520016 single base substitution A G intron_variant THCA-SA 20 61525838 61525838 single base substitution G A synonymous_variant F833F 2499C>T THCA-SA 20 61538601 61538601 single base substitution C T synonymous_variant A424A 1272G>A THCA-SA 20 61569523 61569523 single base substitution G C upstream_gene_variant THCA-US 20 61512289 61512289 single base substitution C G synonymous_variant P1673P 5019G>C THCA-US 20 61524262 61524262 single base substitution G A stop_gained R1052* 3154C>T THCA-US 20 61542301 61542301 single base substitution C T missense_variant D222N 664G>A UCEC-US 20 61510729 61510729 single base substitution C T synonymous_variant R2193R 6579G>A UCEC-US 20 61511059 61511059 insertion of <=200bp - A frameshift_variant F2083F? UCEC-US 20 61511407 61511407 single base substitution G A synonymous_variant F1967F 5901C>T UCEC-US 20 61511540 61511540 single base substitution A C missense_variant F1923C 5768T>G UCEC-US 20 61511641 61511641 single base substitution G A synonymous_variant F1889F 5667C>T UCEC-US 20 61511908 61511908 single base substitution G A synonymous_variant F1800F 5400C>T UCEC-US 20 61512118 61512118 single base substitution G A synonymous_variant G1730G 5190C>T UCEC-US 20 61512169 61512169 single base substitution G A synonymous_variant S1713S 5139C>T UCEC-US 20 61512815 61512815 single base substitution T C missense_variant E1498G 4493A>G UCEC-US 20 61512975 61512975 single base substitution G A missense_variant P1445S 4333C>T UCEC-US 20 61513033 61513033 single base substitution G T synonymous_variant A1425A 4275C>A UCEC-US 20 61513092 61513092 single base substitution G A missense_variant R1406W 4216C>T UCEC-US 20 61513198 61513198 single base substitution G T missense_variant F1370L 4110C>A UCEC-US 20 61513207 61513207 single base substitution G A synonymous_variant F1367F 4101C>T UCEC-US 20 61513328 61513328 single base substitution G T stop_gained S1327* 3980C>A UCEC-US 20 61513427 61513427 single base substitution G T missense_variant A1294E 3881C>A UCEC-US 20 61522306 61522306 single base substitution G A missense_variant R1183C 3547C>T UCEC-US 20 61522306 61522306 single base substitution G A splice_region_variant UCEC-US 20 61522459 61522459 single base substitution C T missense_variant A1132T 3394G>A UCEC-US 20 61525150 61525150 single base substitution T C missense_variant H990R 2969A>G UCEC-US 20 61525431 61525431 single base substitution C T synonymous_variant P896P 2688G>A UCEC-US 20 61525857 61525857 single base substitution G A missense_variant A827V 2480C>T UCEC-US 20 61526413 61526413 single base substitution C G missense_variant R773S 2319G>C UCEC-US 20 61527623 61527623 single base substitution G A missense_variant R726C 2176C>T UCEC-US 20 61527642 61527642 single base substitution A C missense_variant N719K 2157T>G UCEC-US 20 61527926 61527926 single base substitution G A missense_variant R671W 2011C>T UCEC-US 20 61527945 61527945 single base substitution C T synonymous_variant S664S 1992G>A UCEC-US 20 61528071 61528071 single base substitution C A synonymous_variant T622T 1866G>T UCEC-US 20 61528135 61528135 single base substitution G A missense_variant S601F 1802C>T UCEC-US 20 61528315 61528315 single base substitution G A missense_variant A541V 1622C>T UCEC-US 20 61536912 61536912 single base substitution C T 3_prime_UTR_variant UCEC-US 20 61536912 61536912 single base substitution C T intron_variant UCEC-US 20 61536912 61536912 single base substitution C T missense_variant A544T 1630G>A UCEC-US 20 61537259 61537259 single base substitution G A missense_variant S523L 1568C>T UCEC-US 20 61538602 61538602 single base substitution G A missense_variant A424V 1271C>T UCEC-US 20 61538656 61538656 single base substitution G A missense_variant A406V 1217C>T UCEC-US 20 61541129 61541129 single base substitution G A synonymous_variant S361S 1083C>T UCEC-US 20 61541305 61541305 single base substitution G A stop_gained R303* 907C>T UCEC-US 20 61542423 61542423 single base substitution A C missense_variant L181R 542T>G UCEC-US 20 61542781 61542781 single base substitution G A missense_variant R62W 184C>T UCEC-US 20 61542793 61542793 single base substitution C A missense_variant G58C 172G>T UCEC-US 20 61542940 61542940 single base substitution T C missense_variant N9D 25A>G UCEC-US 20 61572885 61572885 single base substitution A G upstream_gene_variant

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand TCGA-AC-A23H-01 COSM342371 c.2511G>C p.L837F Substitution - Missense 20:62894474-62894474 - Pat_16_B COSM5858304 c.5473G>A p.G1825S Substitution - Missense 20:62880483-62880483 - SW48 COSM2931286 c.893G>A p.G298D Substitution - Missense 20:62909967-62909967 - TCGA-AP-A054-01 COSM1028996 c.1217C>T p.A406V Substitution - Missense 20:62907304-62907304 - TCGA-59-2372-01 COSM1327506 c.5199C>T p.T1733T Substitution - coding silent 20:62880757-62880757 - ME020T COSM225800 c.1658C>T p.P553L Substitution - Missense 20:62896927-62896927 - CSCC-45-T COSM4500740 c.5727C>T p.P1909P Substitution - coding silent 20:62880229-62880229 - PD11742a COSM5776402 c.5962C>A p.Q1988K Substitution - Missense 20:62879994-62879994 - Pat_16_A COSM5858304 c.5473G>A p.G1825S Substitution - Missense 20:62880483-62880483 - PT18_1 COSM5899330 c.4159C>T p.P1387S Substitution - Missense 20:62881797-62881797 - T3262 COSM4677512 c.2407G>T p.E803* Substitution - Nonsense 20:62894839-62894839 - SCC-25 COSM4591406 c.4867G>A p.E1623K Substitution - Missense 20:62881089-62881089 - 2557_PT COSM444188 c.4516G>A p.A1506T Substitution - Missense 20:62881440-62881440 - TCGA-GV-A3QK-01 COSM3799749 c.1052C>T p.T351I Substitution - Missense 20:62909808-62909808 - LC_C6 COSM1190310 c.1094G>T p.G365V Substitution - Missense 20:62909766-62909766 - 8066482 COSM3770872 c.5597C>T p.A1866V Substitution - Missense 20:62880359-62880359 - TCGA-B5-A0JY-01 COSM1028965 c.5901C>T p.F1967F Substitution - coding silent 20:62880055-62880055 - TCGA-CM-6171-01 COSM1413010 c.5812C>T p.R1938W Substitution - Missense 20:62880144-62880144 - ESO-037 COSM1250074 c.1359G>A p.P453P Substitution - coding silent 20:62907162-62907162 - TCGA-BP-4352-01 COSM3363364 c.2163C>T p.Y721Y Substitution - coding silent 20:62896284-62896284 - TCGA-AX-A05Z-01 COSM1028986 c.2176C>T p.R726C Substitution - Missense 20:62896271-62896271 - MOLT-4 COSM1681831 c.3986A>T p.D1329V Substitution - Missense 20:62881970-62881970 - TCGA-BR-4361-01 COSM4100193 c.2540A>G p.H847R Substitution - Missense 20:62894445-62894445 - TCGA-DK-A3X1-01 COSM3799744 c.4324G>C p.D1442H Substitution - Missense 20:62881632-62881632 - ICC008T COSM2931086 c.5339C>T p.P1780L Substitution - Missense 20:62880617-62880617 - TCGA-AP-A056-01 COSM1028995 c.1271C>T p.A424V Substitution - Missense 20:62907250-62907250 - 8015745 COSM3389890 c.1784C>G p.P595R Substitution - Missense 20:62896801-62896801 - UD-SCC-2 COSM4603233 c.4878_4879insC p.A1627fs*53 Insertion - Frameshift 20:62881077-62881078 - TCGA-GD-A2C5-01 COSM1307614 c.1511C>T p.S504L Substitution - Missense 20:62905964-62905964 - TCGA-EE-A2GC-06 COSM1713785 c.2914C>T p.P972S Substitution - Missense 20:62893853-62893853 - CSCC-49-T COSM4488952 c.3404C>T p.S1135F Substitution - Missense 20:62891097-62891097 - WSU-HN13 COSM4293948 c.4924A>C p.T1642P Substitution - Missense 20:62881032-62881032 - TCGA-ER-A19A-06 COSM3548789 c.3857C>T p.P1286L Substitution - Missense 20:62882099-62882099 - TCGA-BR-8081-01 COSM4100187 c.4217G>A p.R1406Q Substitution - Missense 20:62881739-62881739 - CSCC-5-T COSM4541323 c.2984G>C p.R995T Substitution - Missense 20:62893783-62893783 - CHC1545T COSM4787512 c.2006A>G p.Q669R Substitution - Missense 20:62896579-62896579 - 2521262 COSM5892434 c.6074C>T p.P2025L Substitution - Missense 20:62879882-62879882 - CSCC-45-T COSM4501454 c.5891C>T p.P1964L Substitution - Missense 20:62880065-62880065 - AOCS-088-3-8 COSM4137120 c.5301C>T p.H1767H Substitution - coding silent 20:62880655-62880655 - TCGA-AG-3999-01 COSM258883 c.5648G>T p.G1883V Substitution - Missense 20:62880308-62880308 - SCC-25 COSM4591407 c.4872G>C p.K1624N Substitution - Missense 20:62881084-62881084 - CSCC-44-T COSM4498959 c.5313C>T p.F1771F Substitution - coding silent 20:62880643-62880643 - WSU-HN8 COSM4591407 c.4872G>C p.K1624N Substitution - Missense 20:62881084-62881084 - T2940 COSM4677496 c.6317A>G p.Q2106R Substitution - Missense 20:62879639-62879639 - Pat_66_A COSM3423807 c.3914C>T p.S1305L Substitution - Missense 20:62882042-62882042 - TCGA-HC-A4ZV-01 COSM3673160 c.3707A>G p.Q1236R Substitution - Missense 20:62882249-62882249 - TCGA-BP-4759-01 COSM3363362 c.2301T>C p.L767L Substitution - coding silent 20:62895079-62895079 - YUCLAT COSM1713786 c.1702C>T p.P568S Substitution - Missense 20:62896883-62896883 - TCGA-BR-4257-01 COSM4100177 c.6296C>A p.P2099Q Substitution - Missense 20:62879660-62879660 - CHC1545T COSM4787512 c.2006A>G p.Q669R Substitution - Missense 20:62896579-62896579 - TCGA-66-2727-01 COSM724842 c.5546A>T p.H1849L Substitution - Missense 20:62880410-62880410 - CSCC-62-T COSM4484313 c.2797C>T p.P933S Substitution - Missense 20:62893970-62893970 - TCGA-66-2773-01 COSM724840 c.5291C>A p.S1764* Substitution - Nonsense 20:62880665-62880665 - HCC104T COSM1615834 c.1399C>A p.H467N Substitution - Missense 20:62906076-62906076 - pfg043T COSM4756273 c.4097A>T p.Q1366L Substitution - Missense 20:62881859-62881859 - SC_9021 COSM5552625 c.2773G>A p.D925N Substitution - Missense 20:62893994-62893994 - SCC-9 COSM4293948 c.4924A>C p.T1642P Substitution - Missense 20:62881032-62881032 - WSU-HN12 COSM4591407 c.4872G>C p.K1624N Substitution - Missense 20:62881084-62881084 - CN-AML-CR-57-Dx COSM444190 c.1631T>C p.M544T Substitution - Missense 20:62896954-62896954 - TCGA-A8-A09G-01 COSM3841481 c.365G>C p.R122T Substitution - Missense 20:62911248-62911248 - TCGA-BG-A0MQ-01 COSM1028990 c.1866G>T p.T622T Substitution - coding silent 20:62896719-62896719 - T2384 COSM1723061 c.4927_4928insC p.R1643fs*37 Insertion - Frameshift 20:62881028-62881029 - CSCC-37-T COSM4481711 c.2535C>T p.R845R Substitution - coding silent 20:62894450-62894450 - PCSI_0083_Pa_P_526 COSM3379109 c.2067C>T p.S689S Substitution - coding silent 20:62896380-62896380 - TCGA-BR-4183-01 COSM160428 c.4258G>A p.E1420K Substitution - Missense 20:62881698-62881698 - TCGA-AA-3663-01 COSM1028974 c.4216C>T p.R1406W Substitution - Missense 20:62881740-62881740 - 93VU147T COSM4591407 c.4872G>C p.K1624N Substitution - Missense 20:62881084-62881084 - TCGA-BP-4170-01 COSM3363362 c.2301T>C p.L767L Substitution - coding silent 20:62895079-62895079 - TCGA-AP-A051-01 COSM1028997 c.1083C>T p.S361S Substitution - coding silent 20:62909777-62909777 - CRC-03T COSM5451587 c.5538G>T p.K1846N Substitution - Missense 20:62880418-62880418 - ML_103_T_01 COSM127803 c.1740A>C p.T580T Substitution - coding silent 20:62896845-62896845 - 587238 COSM1029000 c.184C>T p.R62W Substitution - Missense 20:62911429-62911429 - 35M COSM1413022 c.2227C>T p.R743C Substitution - Missense 20:62895153-62895153 - sysucc-1163T COSM4677505 c.4407G>A p.T1469T Substitution - coding silent 20:62881549-62881549 - 8030340 COSM3389886 c.6547C>T p.R2183* Substitution - Nonsense 20:62879409-62879409 - T3417 COSM1723061 c.4927_4928insC p.R1643fs*37 Insertion - Frameshift 20:62881028-62881029 - TCGA-FS-A1ZQ-06 COSM3548770 c.6020C>T p.S2007L Substitution - Missense 20:62879936-62879936 - TCGA-BR-8363-01 COSM4100179 c.4866C>T p.G1622G Substitution - coding silent 20:62881090-62881090 - PD9604a COSM5802596 c.5234delG p.G1745fs*119 Deletion - Frameshift 20:62880722-62880722 - TCGA-BS-A0UV-01 COSM1028992 c.1622C>T p.A541V Substitution - Missense 20:62896963-62896963 - BCM339T COSM4802465 c.4581G>A p.S1527S Substitution - coding silent 20:62881375-62881375 - TK10 COSM1684631 c.3862_3873del12 p.T1291_A1294delTTAA Deletion - In frame 20:62882083-62882094 - TCGA-DK-A3WW-01 COSM3799745 c.3192G>C p.Q1064H Substitution - Missense 20:62892872-62892872 - UM-SCC-4 COSM2931315 c.418G>C p.E140Q Substitution - Missense 20:62911195-62911195 - TCGA-66-2773-01 COSM724835 c.4412C>T p.S1471F Substitution - Missense 20:62881544-62881544 - TCGA-D9-A148-06 COSM3548776 c.5359G>A p.A1787T Substitution - Missense 20:62880597-62880597 - PD11742a COSM5776430 c.1880A>T p.K627M Substitution - Missense 20:62896705-62896705 - CSCC-18-T COSM4497695 c.502C>T p.L168F Substitution - Missense 20:62911111-62911111 - TCGA-GV-A3JX-01 COSM1307608 c.4509G>A p.Q1503Q Substitution - coding silent 20:62881447-62881447 - TCGA-BR-4368-01 COSM4100199 c.1804G>A p.A602T Substitution - Missense 20:62896781-62896781 - CSCC-7-T COSM4478266 c.2224C>T p.H742Y Substitution - Missense 20:62895156-62895156 - NOKSI COSM4603233 c.4878_4879insC p.A1627fs*53 Insertion - Frameshift 20:62881077-62881078 - PTC-7C COSM4134759 c.1140G>A p.K380K Substitution - coding silent 20:62909720-62909720 - 2521252 COSM5889395 c.3185A>C p.N1062T Substitution - Missense 20:62892879-62892879 - TCGA-J9-A52C-01 COSM4877641 c.3637G>A p.E1213K Substitution - Missense 20:62882319-62882319 - TCGA-AN-A046-01 COSM3841469 c.1389C>A p.I463I Substitution - coding silent 20:62906086-62906086 - pfg375T COSM4756268 c.6637G>A p.D2213N Substitution - Missense 20:62879319-62879319 - HCT15 COSM4624315 c.175C>T p.L59L Substitution - coding silent 20:62911438-62911438 - TCGA-BR-4361-01 COSM4100225 c.246G>A p.R82R Substitution - coding silent 20:62911367-62911367 - 166 COSM3721478 c.5574C>T p.A1858A Substitution - coding silent 20:62880382-62880382 - 8015299 COSM1168959 c.500G>A p.R167H Substitution - Missense 20:62911113-62911113 - ESO-1154 COSM1250078 c.1087G>T p.D363Y Substitution - Missense 20:62909773-62909773 - TCGA-DK-A2I4-01 COSM1534244 c.5158G>A p.E1720K Substitution - Missense 20:62880798-62880798 - TCGA-DA-A1I8-06 COSM3548825 c.88C>T p.R30* Substitution - Nonsense 20:62911525-62911525 - CSCC-6-T COSM4550247 c.4968G>A p.R1656R Substitution - coding silent 20:62880988-62880988 - ESCC_31 COSM1534243 c.4751G>A p.R1584H Substitution - Missense 20:62881205-62881205 - YUZINO COSM1713782 c.4037C>T p.P1346L Substitution - Missense 20:62881919-62881919 - HX31T COSM3707921 c.2917A>G p.S973G Substitution - Missense 20:62893850-62893850 - CSCC-11-T COSM4484555 c.2823C>T p.S941S Substitution - coding silent 20:62893944-62893944 - TCGA-CG-5723-01 COSM4100185 c.4351G>T p.D1451Y Substitution - Missense 20:62881605-62881605 - RKO COSM4440603 c.6101delC p.P2034fs*>207 Deletion - Frameshift 20:62879855-62879855 - ME009T COSM224062 c.3119C>T p.S1040F Substitution - Missense 20:62892945-62892945 - TCGA-FV-A4ZQ-01 COSM4921936 c.4404G>T p.A1468A Substitution - coding silent 20:62881552-62881552 - TCGA-24-1463-01 COSM74378 c.1246G>A p.D416N Substitution - Missense 20:62907275-62907275 - ESCC_BICR_003T COSM5442691 c.4107G>C p.Q1369H Substitution - Missense 20:62881849-62881849 - TCGA-EI-6507-01 COSM1566161 c.4057G>A p.G1353R Substitution - Missense 20:62881899-62881899 - TCGA-BS-A0UJ-01 COSM1028971 c.4493A>G p.E1498G Substitution - Missense 20:62881463-62881463 - DLD1 COSM4624313 c.3751G>A p.A1251T Substitution - Missense 20:62882205-62882205 - TCGA-EI-6882-01 COSM1028988 c.2011C>T p.R671W Substitution - Missense 20:62896574-62896574 - TCGA-KK-A59V-01 COSM4100176 c.6326C>T p.A2109V Substitution - Missense 20:62879630-62879630 - YUKAT COSM5392553 c.1903G>A p.V635M Substitution - Missense 20:62896682-62896682 - 526LT COSM149207 c.1666G>A p.A556T Substitution - Missense 20:62896919-62896919 - CSCC-16-T COSM4500388 c.5649C>T p.G1883G Substitution - coding silent 20:62880307-62880307 - 2557_CLM COSM444188 c.4516G>A p.A1506T Substitution - Missense 20:62881440-62881440 - 8016470 COSM3389892 c.444C>T p.H148H Substitution - coding silent 20:62911169-62911169 - TCGA-BH-A18V-06 COSM3841467 c.1691G>C p.R564T Substitution - Missense 20:62896894-62896894 - TCGA-B7-5816-01 COSM4100190 c.3785C>T p.P1262L Substitution - Missense 20:62882171-62882171 - TCGA-BR-8680-01 COSM3423807 c.3914C>T p.S1305L Substitution - Missense 20:62882042-62882042 - sysucc-1370T COSM5471245 c.5977C>T p.R1993W Substitution - Missense 20:62879979-62879979 - 8069156 COSM3770874 c.3496G>A p.A1166T Substitution - Missense 20:62891005-62891005 - TCGA-D3-A2JK-06 COSM252474 c.1358C>T p.P453L Substitution - Missense 20:62907163-62907163 - TCGA-AN-A04C-01 COSM5834006 c.1389_1390insA p.S464fs*27 Insertion - Frameshift 20:62906085-62906086 - TCGA-D1-A17Q-01 COSM1028967 c.5667C>T p.F1889F Substitution - coding silent 20:62880289-62880289 - Pat_05_B COSM1723061 c.4927_4928insC p.R1643fs*37 Insertion - Frameshift 20:62881028-62881029 - ESCC_115 COSM5639790 c.5973A>G p.G1991G Substitution - coding silent 20:62879983-62879983 - TCGA-EE-A3JA-06 COSM3548790 c.3802C>T p.P1268S Substitution - Missense 20:62882154-62882154 - TCGA-22-4613-01 COSM724827 c.2553C>T p.L851L Substitution - coding silent 20:62894432-62894432 - PTC-14C COSM4134750 c.5388G>C p.P1796P Substitution - coding silent 20:62880568-62880568 - T2944 COSM4677529 c.575G>A p.R192H Substitution - Missense 20:62911038-62911038 - CSCC-11-T COSM4449726 c.3131delG p.G1044fs*76 Deletion - Frameshift 20:62892933-62892933 - Pat_76_A COSM5858305 c.3881C>T p.A1294V Substitution - Missense 20:62882075-62882075 - TCGA-AX-A0J0-01 COSM1028975 c.4110C>A p.F1370L Substitution - Missense 20:62881846-62881846 - PS-286-7D COSM4423934 c.6121T>C p.W2041R Substitution - Missense 20:62879835-62879835 - LS411 COSM2931214 c.1545G>T p.K515N Substitution - Missense 20:62905930-62905930 - CPCG0371-F1 COSM4966344 c.1174C>T p.P392S Substitution - Missense 20:62907347-62907347 - YUFOLD COSM1713785 c.2914C>T p.P972S Substitution - Missense 20:62893853-62893853 - HCT-15 COSM1681834 c.1834A>G p.R612G Substitution - Missense 20:62896751-62896751 - SNUH_G45_S1 COSM2931235 c.1290C>T p.S430S Substitution - coding silent 20:62907231-62907231 - TCGA-D9-A6EC-06 COSM4401384 c.2581C>T p.P861S Substitution - Missense 20:62894186-62894186 - PCSI_0083_Pa_P COSM3379109 c.2067C>T p.S689S Substitution - coding silent 20:62896380-62896380 - TCGA-A5-A0VQ-01 COSM1028994 c.1502G>C p.S501T Substitution - Missense 20:62905973-62905973 - SC_9047 COSM5556962 c.5356A>G p.I1786V Substitution - Missense 20:62880600-62880600 - ESOSCC152T COSM1172739 c.374C>A p.P125H Substitution - Missense 20:62911239-62911239 - TCGA-BR-4257-01 COSM2931186 c.1889G>A p.G630D Substitution - Missense 20:62896696-62896696 - TCGA-33-4586-01 COSM724834 c.4117G>T p.D1373Y Substitution - Missense 20:62881839-62881839 - TCGA-DK-A3IL-01 COSM1307610 c.4236G>C p.R1412S Substitution - Missense 20:62881720-62881720 - TCGA-D5-6928-01 COSM1413022 c.2227C>T p.R743C Substitution - Missense 20:62895153-62895153 - HCA46 COSM4611938 c.1715delC p.S572fs*67 Deletion - Frameshift 20:62896870-62896870 - TCGA-D1-A17Q-01 COSM1028976 c.4101C>T p.F1367F Substitution - coding silent 20:62881855-62881855 - NCI-H727 COSM2931057 c.6319G>T p.G2107C Substitution - Missense 20:62879637-62879637 - TCGA-HU-A4H4-01 COSM4100217 c.622A>G p.T208A Substitution - Missense 20:62910991-62910991 - T670 COSM4677495 c.6358G>A p.G2120S Substitution - Missense 20:62879598-62879598 - TCGA-13-1512-01 COSM70449 c.998C>T p.A333V Substitution - Missense 20:62909862-62909862 - HCC104 COSM1615834 c.1399C>A p.H467N Substitution - Missense 20:62906076-62906076 - BK0033 COSM4186981 c.2306C>T p.T769M Substitution - Missense 20:62895074-62895074 - TCGA-EE-A3AG-06 COSM3548771 c.5996C>T p.S1999F Substitution - Missense 20:62879960-62879960 - TCGA-CG-5721-01 COSM4100191 c.2893G>T p.G965C Substitution - Missense 20:62893874-62893874 - TCGA-MU-A5YI-01 COSM4855263 c.4253C>A p.A1418E Substitution - Missense 20:62881703-62881703 - CAL33 COSM4603233 c.4878_4879insC p.A1627fs*53 Insertion - Frameshift 20:62881077-62881078 - Pat_41_B COSM5858303 c.5854G>A p.A1952T Substitution - Missense 20:62880102-62880102 - LUAD-LIP77 COSM342371 c.2511G>C p.L837F Substitution - Missense 20:62894474-62894474 - TCGA-D5-6928-01 COSM1413007 c.6258G>T p.R2086S Substitution - Missense 20:62879698-62879698 - BN45T COSM1615832 c.3116G>T p.R1039L Substitution - Missense 20:62892948-62892948 - TCGA-DA-A1HY-06 COSM3548777 c.5339C>G p.P1780R Substitution - Missense 20:62880617-62880617 - HCC18 COSM1615831 c.5010C>T p.P1670P Substitution - coding silent 20:62880946-62880946 - TCGA-AP-A0LM-01 COSM1028980 c.3394G>A p.A1132T Substitution - Missense 20:62891107-62891107 - BICR_22 COSM4603233 c.4878_4879insC p.A1627fs*53 Insertion - Frameshift 20:62881077-62881078 - TCGA-HU-A4GT-01 COSM2931179 c.2236C>T p.R746C Substitution - Missense 20:62895144-62895144 - TCGA-G4-6321-01 COSM3758729 c.4702A>G p.T1568A Substitution - Missense 20:62881254-62881254 - CSCC-35-T COSM4565946 c.275_276CC>TT p.S92F Substitution - Missense 20:62911337-62911338 - LUAD-RT-S01702 COSM379271 c.188G>A p.R63H Substitution - Missense 20:62911425-62911425 - BRC13 COSM5028728 c.3307T>A p.W1103R Substitution - Missense 20:62892025-62892025 - I2L-P7-Tumor-Organoid COSM4677507 c.3797delC p.P1266fs*8 Deletion - Frameshift 20:62882159-62882159 - TCGA-GN-A266-06 COSM2931086 c.5339C>T p.P1780L Substitution - Missense 20:62880617-62880617 - 3206A7_017_T COSM5038714 c.2541_2568del28 p.H847fs*28 Deletion - Frameshift 20:62894417-62894444 - TCGA-EE-A182-06 COSM3548781 c.4952C>T p.S1651L Substitution - Missense 20:62881004-62881004 - PT35 COSM5914282 c.5792C>T p.P1931L Substitution - Missense 20:62880164-62880164 - TCGA-AP-A059-01 COSM1028978 c.3881C>A p.A1294E Substitution - Missense 20:62882075-62882075 - PD11372a COSM5767176 c.2493C>T p.D831D Substitution - coding silent 20:62894492-62894492 - TCGA-AA-A010-01 COSM280384 c.4310C>T p.A1437V Substitution - Missense 20:62881646-62881646 - TCGA-EE-A2MS-06 COSM3548768 c.6380G>A p.R2127Q Substitution - Missense 20:62879576-62879576 - TCGA-A6-6781-01 COSM1413027 c.1681C>T p.P561S Substitution - Missense 20:62896904-62896904 - PR-00-1165 COSM244038 c.2417C>T p.P806L Substitution - Missense 20:62894829-62894829 - 2_RESISTANT COSM1723061 c.4927_4928insC p.R1643fs*37 Insertion - Frameshift 20:62881028-62881029 - SC_9008 COSM3548770 c.6020C>T p.S2007L Substitution - Missense 20:62879936-62879936 - TCGA-HT-7884-01 COSM3972661 c.5316G>A p.P1772P Substitution - coding silent 20:62880640-62880640 - TCGA-29-1770-01 COSM1327504 c.400G>C p.E134Q Substitution - Missense 20:62911213-62911213 - 1_RESISTANT COSM1721203 c.6686C>T p.S2229L Substitution - Missense 20:62879270-62879270 - TCGA-FD-A3SO-01 COSM1649942 c.4225G>A p.E1409K Substitution - Missense 20:62881731-62881731 - TCGA-AA-3821-01 COSM294310 c.1172C>T p.A391V Substitution - Missense 20:62907349-62907349 - TCGA-D9-A6EC-06 COSM4401765 c.1570C>T p.P524S Substitution - Missense 20:62905905-62905905 - UM-SCC-2 COSM4591406 c.4867G>A p.E1623K Substitution - Missense 20:62881089-62881089 - CSCC-27-T COSM4495451 c.4542C>T p.F1514F Substitution - coding silent 20:62881414-62881414 - TCGA-AY-6196-01 COSM1413013 c.5213C>T p.P1738L Substitution - Missense 20:62880743-62880743 - SH-0622 COSM5017382 c.4928_4929insC p.A1645fs*35 Insertion - Frameshift 20:62881027-62881028 - SCC-25 COSM4293948 c.4924A>C p.T1642P Substitution - Missense 20:62881032-62881032 - TCGA-AZ-4615-01 COSM3693629 c.6184G>A p.D2062N Substitution - Missense 20:62879772-62879772 - 60T COSM107386 c.3988C>T p.P1330S Substitution - Missense 20:62881968-62881968 - TCGA-F5-6814-01 COSM3371751 c.664G>A p.D222N Substitution - Missense 20:62910949-62910949 - ZZUFHECRKL-G034T COSM5440266 c.2063A>C p.D688A Substitution - Missense 20:62896384-62896384 - TCGA-EB-A3XD-01 COSM3548793 c.3165C>T p.T1055T Substitution - coding silent 20:62892899-62892899 - RKO COSM2931093 c.5228delT p.V1743fs*121 Deletion - Frameshift 20:62880728-62880728 - TCGA-ER-A19F-06 COSM2931087 c.5320C>T p.P1774S Substitution - Missense 20:62880636-62880636 - T3021 COSM4677507 c.3797delC p.P1266fs*8 Deletion - Frameshift 20:62882159-62882159 - PCSI_0139_Pa_X COSM3379108 c.6489C>T p.A2163A Substitution - coding silent 20:62879467-62879467 - ATL001 COSM5707509 c.3356T>A p.L1119Q Substitution - Missense 20:62891145-62891145 - TCGA-G4-6293-01 COSM3758728 c.4932C>T p.P1644P Substitution - coding silent 20:62881024-62881024 - BHY COSM4603233 c.4878_4879insC p.A1627fs*53 Insertion - Frameshift 20:62881077-62881078 - CHC1207T COSM4800152 c.2959G>C p.D987H Substitution - Missense 20:62893808-62893808 - BD165T COSM5506012 c.4927C>T p.R1643C Substitution - Missense 20:62881029-62881029 - TCGA-EB-A41A-01 COSM3548791 c.3791C>T p.P1264L Substitution - Missense 20:62882165-62882165 - WSU-HN8 COSM4603233 c.4878_4879insC p.A1627fs*53 Insertion - Frameshift 20:62881077-62881078 - HCC157 COSM3707918 c.3204A>G p.K1068K Substitution - coding silent 20:62892860-62892860 - CSCC-19-T COSM4549473 c.4739G>A p.R1580K Substitution - Missense 20:62881217-62881217 - LUAD-NYU195 COSM371125 c.4749A>T p.A1583A Substitution - coding silent 20:62881207-62881207 - 2492723 COSM5723153 c.6713C>T p.S2238L Substitution - Missense 20:62879243-62879243 - LUAD-NYU284 COSM373068 c.1148A>C p.K383T Substitution - Missense 20:62909712-62909712 - LUAD-E01317 COSM403772 c.4732C>T p.L1578F Substitution - Missense 20:62881224-62881224 - TCGA-EE-A2MJ-06 COSM3548807 c.1610C>T p.S537F Substitution - Missense 20:62896975-62896975 - TCGA-HT-7884-01 COSM3972660 c.5347G>A p.E1783K Substitution - Missense 20:62880609-62880609 - SNU-C2B COSM1028981 c.3218C>T p.A1073V Substitution - Missense 20:62892846-62892846 - TCGA-G4-6628-01 COSM1413018 c.3627C>T p.D1209D Substitution - coding silent 20:62882329-62882329 - TCGA-AP-A059-01 COSM1028993 c.1568C>T p.S523L Substitution - Missense 20:62905907-62905907 - TCGA-66-2765-01 COSM724839 c.4707G>A p.E1569E Substitution - coding silent 20:62881249-62881249 - 254891 COSM3724844 c.4372G>T p.E1458* Substitution - Nonsense 20:62881584-62881584 - LUAD-B01102 COSM333176 c.250C>T p.R84C Substitution - Missense 20:62911363-62911363 - GC10_T COSM149207 c.1666G>A p.A556T Substitution - Missense 20:62896919-62896919 - TCGA-D9-A149-06 COSM3911763 c.638T>C p.L213P Substitution - Missense 20:62910975-62910975 - BCM339T COSM4802465 c.4581G>A p.S1527S Substitution - coding silent 20:62881375-62881375 - 549 COSM5613010 c.4086G>T p.P1362P Substitution - coding silent 20:62881870-62881870 - TCGA-D1-A167-01 COSM1028984 c.2480C>T p.A827V Substitution - Missense 20:62894505-62894505 - HCT8 COSM4634557 c.1008G>T p.Q336H Substitution - Missense 20:62909852-62909852 - LUAD-S01315 COSM345162 c.5893C>G p.Q1965E Substitution - Missense 20:62880063-62880063 - 93VU147T COSM4591406 c.4867G>A p.E1623K Substitution - Missense 20:62881089-62881089 - TCGA-EE-A2MR-06 COSM3548800 c.1910C>T p.A637V Substitution - Missense 20:62896675-62896675 - TCGA-D8-A1XK-01 COSM2931351 c.129G>A p.A43A Substitution - coding silent 20:62911484-62911484 - YUKSI COSM5392548 c.3951C>T p.I1317I Substitution - coding silent 20:62882005-62882005 - 60T COSM109496 c.3989C>T p.P1330L Substitution - Missense 20:62881967-62881967 - 37M COSM5583436 c.1527C>A p.H509Q Substitution - Missense 20:62905948-62905948 - ESO16T COSM1172738 c.6596G>A p.R2199Q Substitution - Missense 20:62879360-62879360 - TCGA-B5-A11E-01 COSM1028973 c.4275C>A p.A1425A Substitution - coding silent 20:62881681-62881681 - HCC079T COSM5807969 c.334G>T p.E112* Substitution - Nonsense 20:62911279-62911279 - TCGA-AF-2689-01 COSM287709 c.453C>T p.T151T Substitution - coding silent 20:62911160-62911160 - T231 COSM4677500 c.5058G>A p.P1686P Substitution - coding silent 20:62880898-62880898 - BN37 COSM1615833 c.2536G>T p.A846S Substitution - Missense 20:62894449-62894449 - NPC2F COSM4996040 c.3189G>T p.M1063I Substitution - Missense 20:62892875-62892875 - 224 COSM4425641 c.862T>C p.C288R Substitution - Missense 20:62909998-62909998 - T2269 COSM4677514 c.2043T>G p.I681M Substitution - Missense 20:62896542-62896542 - MOLT-4 COSM1681832 c.3559C>T p.P1187S Substitution - Missense 20:62882397-62882397 - TCGA-EE-A3JB-06 COSM4898760 c.6338G>A p.R2113K Substitution - Missense 20:62879618-62879618 - PD18247a COSM5793758 c.6388G>A p.D2130N Substitution - Missense 20:62879568-62879568 - TCGA-D1-A103-01 COSM1028974 c.4216C>T p.R1406W Substitution - Missense 20:62881740-62881740 - LUAD-E01317 COSM403773 c.4605C>G p.F1535L Substitution - Missense 20:62881351-62881351 - B54-Tumor COSM3933908 c.1807A>C p.T603P Substitution - Missense 20:62896778-62896778 - UM-SCC-2 COSM4603233 c.4878_4879insC p.A1627fs*53 Insertion - Frameshift 20:62881077-62881078 - TCGA-B5-A0K9-01 COSM1028981 c.3218C>T p.A1073V Substitution - Missense 20:62892846-62892846 - LUAD-B01169 COSM333636 c.5969G>A p.G1990D Substitution - Missense 20:62879987-62879987 - 587284 COSM1203598 c.4172A>G p.Y1391C Substitution - Missense 20:62881784-62881784 - TCGA-AY-6196-01 COSM1413026 c.1738A>T p.T580S Substitution - Missense 20:62896847-62896847 - LUAD-RT-S01852 COSM384940 c.4485G>T p.E1495D Substitution - Missense 20:62881471-62881471 - MN-1045 COSM1578837 c.4066G>T p.A1356S Substitution - Missense 20:62881890-62881890 - YUKAT COSM5392555 c.1137G>A p.K379K Substitution - coding silent 20:62909723-62909723 - KPOPBR-24-T COSM5964200 c.5562G>A p.E1854E Substitution - coding silent 20:62880394-62880394 - 61 COSM5741939 c.4175A>G p.D1392G Substitution - Missense 20:62881781-62881781 - SCC-15 COSM4603233 c.4878_4879insC p.A1627fs*53 Insertion - Frameshift 20:62881077-62881078 - BN24T COSM1615837 c.128C>T p.A43V Substitution - Missense 20:62911485-62911485 - sysucc-1397T COSM5474298 c.243G>A p.A81A Substitution - coding silent 20:62911370-62911370 - AD70 COSM5966784 c.883G>T p.D295Y Substitution - Missense 20:62909977-62909977 - 1T COSM106611 c.4008C>T p.P1336P Substitution - coding silent 20:62881948-62881948 - TCGA-BS-A0UV-01 COSM1028968 c.5400C>T p.F1800F Substitution - coding silent 20:62880556-62880556 - TCGA-D7-A4YY-01 COSM4100182 c.4521C>T p.V1507V Substitution - coding silent 20:62881435-62881435 - TCGA-85-6560-01 COSM724826 c.2104A>G p.I702V Substitution - Missense 20:62896343-62896343 - B81-2-Tumor COSM1757015 c.4470G>C p.K1490N Substitution - Missense 20:62881486-62881486 - CSCC-27-T COSM4496896 c.4854C>T p.P1618P Substitution - coding silent 20:62881102-62881102 - TCGA-C8-A132-01 COSM444189 c.3345+1G>C p.? Unknown 20:62891986-62891986 - TCGA-EE-A29E-06 COSM2931295 c.657C>T p.P219P Substitution - coding silent 20:62910956-62910956 - LP6005409-DNA_E02 COSM4411501 c.5523A>G p.Q1841Q Substitution - coding silent 20:62880433-62880433 - TCGA-F5-6814-01 COSM3423807 c.3914C>T p.S1305L Substitution - Missense 20:62882042-62882042 - TCGA-66-2773-01 COSM160424 c.5239C>G p.Q1747E Substitution - Missense 20:62880717-62880717 - AOCS-088-1-0 COSM4137120 c.5301C>T p.H1767H Substitution - coding silent 20:62880655-62880655 - OV207 COSM252474 c.1358C>T p.P453L Substitution - Missense 20:62907163-62907163 - PT08_2 COSM5894078 c.4072C>T p.P1358S Substitution - Missense 20:62881884-62881884 - TCGA-AM-5820-01 COSM3693631 c.4896C>T p.D1632D Substitution - coding silent 20:62881060-62881060 - TCGA-AA-A010-01 COSM280386 c.3393C>T p.V1131V Substitution - coding silent 20:62891108-62891108 - HCT15 COSM1681834 c.1834A>G p.R612G Substitution - Missense 20:62896751-62896751 - B66-0 COSM1751551 c.1738A>C p.T580P Substitution - Missense 20:62896847-62896847 - TCGA-66-2759-01 COSM724824 c.1791G>A p.R597R Substitution - coding silent 20:62896794-62896794 - TCGA-27-1836-01 COSM3405266 c.4988C>T p.P1663L Substitution - Missense 20:62880968-62880968 - PD4203a COSM160427 c.6352G>A p.E2118K Substitution - Missense 20:62879604-62879604 - TCGA-EW-A1PB-01 COSM1483830 c.3482T>G p.L1161R Substitution - Missense 20:62891019-62891019 - 262LT COSM4382112 c.1912G>A p.V638I Substitution - Missense 20:62896673-62896673 - TCGA-ED-A4XI-01 COSM4913174 c.5510T>G p.V1837G Substitution - Missense 20:62880446-62880446 - pfg228T COSM4765817 c.2614_2615insA p.L874fs*6 Insertion - Frameshift 20:62894152-62894153 - TCGA-Q1-A5R2-01 COSM4850274 c.4996G>A p.G1666S Substitution - Missense 20:62880960-62880960 - TCGA-CM-4743-01 COSM1413024 c.1991C>T p.S664L Substitution - Missense 20:62896594-62896594 - TCGA-CC-A7IK-01 COSM4924973 c.4531A>G p.M1511V Substitution - Missense 20:62881425-62881425 - TCGA-BS-A0UF-01 COSM1028966 c.5768T>G p.F1923C Substitution - Missense 20:62880188-62880188 - TCGA-B5-A0JY-01 COSM1028987 c.2157T>G p.N719K Substitution - Missense 20:62896290-62896290 - YUMOKI COSM5392551 c.2465C>T p.P822L Substitution - Missense 20:62894520-62894520 - 61 COSM5741938 c.6556A>T p.R2186W Substitution - Missense 20:62879400-62879400 - TCGA-EE-A183-06 COSM2931063 c.6176C>T p.P2059L Substitution - Missense 20:62879780-62879780 - sysucc-274T COSM5476191 c.4800C>T p.L1600L Substitution - coding silent 20:62881156-62881156 - T464 COSM1723061 c.4927_4928insC p.R1643fs*37 Insertion - Frameshift 20:62881028-62881029 - TCGA-FW-A3R5-06 COSM3911759 c.5543C>T p.P1848L Substitution - Missense 20:62880413-62880413 - ACINAR28 COSM1735038 c.4406C>T p.T1469M Substitution - Missense 20:62881550-62881550 - CSCC-7-T COSM4502369 c.6118C>T p.R2040C Substitution - Missense 20:62879838-62879838 - T3091 COSM1028992 c.1622C>T p.A541V Substitution - Missense 20:62896963-62896963 - STC291 COSM5057490 c.2679C>T p.D893D Substitution - coding silent 20:62894088-62894088 - TCGA-FT-A3EE-01 COSM3799747 c.2133T>A p.F711L Substitution - Missense 20:62896314-62896314 - S02289 COSM5686112 c.2911G>T p.A971S Substitution - Missense 20:62893856-62893856 - SC_9100 COSM5567692 c.6462C>T p.S2154S Substitution - coding silent 20:62879494-62879494 - TCGA-D1-A176-01 COSM1028970 c.5139C>T p.S1713S Substitution - coding silent 20:62880817-62880817 - T3535 COSM2931223 c.1425_1426insA p.E476fs*15 Insertion - Frameshift 20:62906049-62906050 - TCGA-A5-A0GW-01 COSM1028972 c.4333C>T p.P1445S Substitution - Missense 20:62881623-62881623 - TCGA-24-2024-01 COSM119642 c.6175C>G p.P2059A Substitution - Missense 20:62879781-62879781 - LC_C4 COSM1190305 c.5549G>C p.G1850A Substitution - Missense 20:62880407-62880407 - TCGA-CD-5801-01 COSM4100188 c.4180G>A p.E1394K Substitution - Missense 20:62881776-62881776 - BHY COSM4591407 c.4872G>C p.K1624N Substitution - Missense 20:62881084-62881084 - pfg129T COSM3423807 c.3914C>T p.S1305L Substitution - Missense 20:62882042-62882042 - TCGA-D3-A5GN-06 COSM3548769 c.6152C>T p.S2051F Substitution - Missense 20:62879804-62879804 - TCGA-EE-A2GO-06 COSM3548798 c.2380C>T p.P794S Substitution - Missense 20:62894866-62894866 - SCC-9 COSM4603233 c.4878_4879insC p.A1627fs*53 Insertion - Frameshift 20:62881077-62881078 - UM-SCC-2 COSM4591407 c.4872G>C p.K1624N Substitution - Missense 20:62881084-62881084 - TCGA-G2-A2EC-01 COSM1307604 c.5893C>T p.Q1965* Substitution - Nonsense 20:62880063-62880063 - TCGA-D3-A2JL-06 COSM3548773 c.5824C>T p.P1942S Substitution - Missense 20:62880132-62880132 - BD124T COSM5451588 c.4211G>A p.R1404Q Substitution - Missense 20:62881745-62881745 - TCGA-CK-5913-01 COSM1413005 c.6451C>T p.R2151W Substitution - Missense 20:62879505-62879505 - Pat_24_A COSM5858308 c.505C>T p.R169C Substitution - Missense 20:62911108-62911108 - C086 COSM4401765 c.1570C>T p.P524S Substitution - Missense 20:62905905-62905905 - Pat_45_B COSM1718608 c.6046C>T p.P2016S Substitution - Missense 20:62879910-62879910 - 234 COSM3731467 c.3102-1G>T p.? Unknown 20:62892963-62892963 - CSB1 COSM5028727 c.4500C>G p.L1500L Substitution - coding silent 20:62881456-62881456 - TCGA-ER-A19A-06 COSM3548809 c.1525C>T p.H509Y Substitution - Missense 20:62905950-62905950 - TCGA-ER-A3PL-06 COSM3548805 c.1665C>T p.S555S Substitution - coding silent 20:62896920-62896920 - TCGA-AA-3697-01 COSM3758729 c.4702A>G p.T1568A Substitution - Missense 20:62881254-62881254 - TCGA-FP-A4BE-01 COSM2931064 c.6161C>T p.A2054V Substitution - Missense 20:62879795-62879795 - TCGA-AX-A0J0-01 COSM1028989 c.1992G>A p.S664S Substitution - coding silent 20:62896593-62896593 - TCGA-AY-6197-01 COSM1413030 c.1366G>A p.G456S Substitution - Missense 20:62907155-62907155 - TCGA-F1-6177-01 COSM2931138 c.3561G>A p.P1187P Substitution - coding silent 20:62882395-62882395 - 8035740 COSM3389887 c.6486G>A p.E2162E Substitution - coding silent 20:62879470-62879470 - TCGA-66-2785-01 COSM724838 c.4552G>A p.D1518N Substitution - Missense 20:62881404-62881404 - MO_1084 COSM5554644 c.4396G>A p.G1466R Substitution - Missense 20:62881560-62881560 - TCGA-39-5036-01 COSM724823 c.1465A>G p.S489G Substitution - Missense 20:62906010-62906010 - CRC-06T COSM5456836 c.3711G>A p.S1237S Substitution - coding silent 20:62882245-62882245 - TCGA-EL-A3T3-01 COSM3371751 c.664G>A p.D222N Substitution - Missense 20:62910949-62910949 - BHY COSM4591406 c.4867G>A p.E1623K Substitution - Missense 20:62881089-62881089 - TCGA-AC-A23H-01 COSM3841464 c.3192G>A p.Q1064Q Substitution - coding silent 20:62892872-62892872 - TCGA-EE-A29D-06 COSM3548786 c.4148G>A p.R1383K Substitution - Missense 20:62881808-62881808 - PCSI_0048_Pa_P COSM216496 c.2647T>C p.L883L Substitution - coding silent 20:62894120-62894120 - TCGA-AU-6004-01 COSM3693630 c.6101C>T p.P2034L Substitution - Missense 20:62879855-62879855 - PD18024a COSM5777339 c.2332G>C p.V778L Substitution - Missense 20:62894914-62894914 - LUAD-S01302 COSM395888 c.5872G>T p.G1958C Substitution - Missense 20:62880084-62880084 - TCGA-F4-6570-01 COSM1413011 c.5652C>T p.G1884G Substitution - coding silent 20:62880304-62880304 - COLO678 COSM4621525 c.1600G>A p.D534N Substitution - Missense 20:62896985-62896985 - YUSIV COSM5392547 c.4296C>T p.T1432T Substitution - coding silent 20:62881660-62881660 - PT36 COSM459704 c.2332-8C>T p.? Unknown 20:62894922-62894922 - sysucc-1397T COSM5474297 c.6177C>T p.P2059P Substitution - coding silent 20:62879779-62879779 - TCGA-BR-4363-01 COSM4100205 c.943A>G p.I315V Substitution - Missense 20:62909917-62909917 - TCGA-41-3393-01 COSM2931066 c.6119G>A p.R2040H Substitution - Missense 20:62879837-62879837 - T2284 COSM4677510 c.2607G>A p.P869P Substitution - coding silent 20:62894160-62894160 - 2290929 COSM4440603 c.6101delC p.P2034fs*>207 Deletion - Frameshift 20:62879855-62879855 - 8069329 COSM3770873 c.4746G>A p.S1582S Substitution - coding silent 20:62881210-62881210 - T1154 COSM1413028 c.1425delA p.E476fs*4 Deletion - Frameshift 20:62906050-62906050 - 4537_T COSM3963763 c.1940C>T p.P647L Substitution - Missense 20:62896645-62896645 - TCGA-AG-A002-01 COSM260420 c.3154C>T p.R1052* Substitution - Nonsense 20:62892910-62892910 - 08-P8005 COSM4581963 c.3718A>C p.K1240Q Substitution - Missense 20:62882238-62882238 - TCGA-E2-A1L7-01 COSM1483833 c.77C>T p.T26I Substitution - Missense 20:62911536-62911536 - TCGA-AY-6196-01 COSM1413014 c.5206C>T p.L1736F Substitution - Missense 20:62880750-62880750 - I2L-P7-Tumor-Organoid COSM5366096 c.2235G>A p.L745L Substitution - coding silent 20:62895145-62895145 - BD124T COSM5494119 c.6361C>T p.R2121* Substitution - Nonsense 20:62879595-62879595 - TCGA-60-2698-01 COSM724830 c.2761C>T p.H921Y Substitution - Missense 20:62894006-62894006 - 2293783 COSM4609564 c.32A>T p.E11V Substitution - Missense 20:62911581-62911581 - TCGA-CC-A7IJ-01 COSM4924497 c.3425G>A p.S1142N Substitution - Missense 20:62891076-62891076 - 1517_PT COSM5755626 c.28G>A p.E10K Substitution - Missense 20:62911585-62911585 - TCGA-G2-A2EC-01 COSM1307606 c.5426C>A p.S1809Y Substitution - Missense 20:62880530-62880530 - TCGA-DB-A64R-01 COSM3972662 c.2013G>A p.R671R Substitution - coding silent 20:62896572-62896572 - TCGA-ER-A19F-06 COSM3548802 c.1770C>T p.F590F Substitution - coding silent 20:62896815-62896815 - DLD1 COSM4624315 c.175C>T p.L59L Substitution - coding silent 20:62911438-62911438 - UM-SCC-17B COSM4603233 c.4878_4879insC p.A1627fs*53 Insertion - Frameshift 20:62881077-62881078 - TCGA-CF-A3MF-01 COSM1307612 c.2496C>T p.V832V Substitution - coding silent 20:62894489-62894489 - PTC-14C COSM4134763 c.102C>T p.I34I Substitution - coding silent 20:62911511-62911511 - Pat_45_A COSM5858300 c.6541C>T p.R2181C Substitution - Missense 20:62879415-62879415 - pfg016T COSM1641413 c.6006_6007insA p.E2003fs*90 Insertion - Frameshift 20:62879949-62879950 - T96 COSM4677508 c.2841C>T p.S947S Substitution - coding silent 20:62893926-62893926 - PT46 COSM5930010 c.6143C>T p.S2048F Substitution - Missense 20:62879813-62879813 - TCGA-BC-A216-01 COSM4911399 c.1655C>T p.P552L Substitution - Missense 20:62896930-62896930 - YUZEST COSM1713780 c.6665G>A p.R2222Q Substitution - Missense 20:62879291-62879291 - HN_62699 COSM127803 c.1740A>C p.T580T Substitution - coding silent 20:62896845-62896845 - TCGA-CG-5723-01 COSM4100176 c.6326C>T p.A2109V Substitution - Missense 20:62879630-62879630 - PR-00-160 COSM244037 c.1105A>G p.R369G Substitution - Missense 20:62909755-62909755 - PD4120a COSM160425 c.5409G>T p.Q1803H Substitution - Missense 20:62880547-62880547 - WSU-HN12 COSM4603233 c.4878_4879insC p.A1627fs*53 Insertion - Frameshift 20:62881077-62881078 - TCGA-AA-3663-01 COSM1413009 c.6051G>T p.Q2017H Substitution - Missense 20:62879905-62879905 - TCGA-B5-A11E-01 COSM1028999 c.542T>G p.L181R Substitution - Missense 20:62911071-62911071 - TCGA-G2-A2EC-01 COSM1307607 c.4862C>T p.S1621L Substitution - Missense 20:62881094-62881094 - TCGA-EE-A29D-06 COSM3548780 c.4983C>T p.P1661P Substitution - coding silent 20:62880973-62880973 - TCGA-B5-A0JY-01 COSM1028988 c.2011C>T p.R671W Substitution - Missense 20:62896574-62896574 - TCGA-BF-A1Q0-01 COSM3548784 c.4451A>C p.K1484T Substitution - Missense 20:62881505-62881505 - TCGA-AA-3663-01 COSM3758729 c.4702A>G p.T1568A Substitution - Missense 20:62881254-62881254 - TCGA-D7-8570-01 COSM4100213 c.792C>T p.Y264Y Substitution - coding silent 20:62910821-62910821 - TCGA-DK-A1A6-01 COSM1307605 c.5471G>C p.R1824T Substitution - Missense 20:62880485-62880485 - C135 COSM1566159 c.3595delA p.I1199fs*10 Deletion - Frameshift 20:62882361-62882361 - TCGA-AA-3511-01 COSM3758727 c.5682G>A p.R1894R Substitution - coding silent 20:62880274-62880274 - TCGA-EE-A2MI-06 COSM3548775 c.5402G>A p.G1801E Substitution - Missense 20:62880554-62880554 - BN24 COSM1615837 c.128C>T p.A43V Substitution - Missense 20:62911485-62911485 - 587228 COSM1203594 c.6619C>T p.R2207W Substitution - Missense 20:62879337-62879337 - PD4119a COSM160424 c.5239C>G p.Q1747E Substitution - Missense 20:62880717-62880717 - TCGA-G2-A2EO-01 COSM1307613 c.2239G>C p.E747Q Substitution - Missense 20:62895141-62895141 - TCGA-FS-A1ZA-06 COSM3911758 c.6291G>A p.E2097E Substitution - coding silent 20:62879665-62879665 - Pat_24_A COSM5858302 c.5875C>T p.P1959S Substitution - Missense 20:62880081-62880081 - TCGA-13-0924-01 COSM74377 c.1979G>A p.S660N Substitution - Missense 20:62896606-62896606 - T2197 COSM269013 c.633C>T p.G211G Substitution - coding silent 20:62910980-62910980 - I2L-P20-Tumor-Biopsy COSM1723061 c.4927_4928insC p.R1643fs*37 Insertion - Frameshift 20:62881028-62881029 - PT37 COSM5921679 c.3413C>T p.S1138F Substitution - Missense 20:62891088-62891088 - CHC892T COSM4958552 c.1478G>A p.G493E Substitution - Missense 20:62905997-62905997 - ESO-859 COSM1238674 c.1698C>T p.L566L Substitution - coding silent 20:62896887-62896887 - HCT8 COSM4624313 c.3751G>A p.A1251T Substitution - Missense 20:62882205-62882205 - DLD1 COSM4624314 c.3689A>C p.K1230T Substitution - Missense 20:62882267-62882267 - TCGA-MY-A5BD-01 COSM4855522 c.2737G>A p.E913K Substitution - Missense 20:62894030-62894030 - TCGA-66-2773-01 COSM724837 c.4413C>T p.S1471S Substitution - coding silent 20:62881543-62881543 - B47-Tumor COSM3933907 c.4351G>C p.D1451H Substitution - Missense 20:62881605-62881605 - TCGA-D9-A4Z3-01 COSM3548817 c.558T>C p.S186S Substitution - coding silent 20:62911055-62911055 - TCGA-EE-A2MS-06 COSM3548779 c.5032G>A p.G1678S Substitution - Missense 20:62880924-62880924 - T3503 COSM4677504 c.4515C>T p.A1505A Substitution - coding silent 20:62881441-62881441 - TCGA-EE-A2GR-06 COSM3548772 c.5870C>T p.P1957L Substitution - Missense 20:62880086-62880086 - TCGA-FW-A3R5-06 COSM3911761 c.2723C>T p.P908L Substitution - Missense 20:62894044-62894044 - TCGA-IR-A3LA-01 COSM4844710 c.2362G>A p.E788K Substitution - Missense 20:62894884-62894884 - 2497767 COSM5750138 c.2360A>G p.N787S Substitution - Missense 20:62894886-62894886 - TCGA-EE-A29M-06 COSM724828 c.2630C>T p.S877F Substitution - Missense 20:62894137-62894137 - NOKSI COSM4293948 c.4924A>C p.T1642P Substitution - Missense 20:62881032-62881032 - SJHYPO039 COSM4775659 c.6165C>T p.P2055P Substitution - coding silent 20:62879791-62879791 - AOCS-149-1-7 COSM4137121 c.117C>T p.G39G Substitution - coding silent 20:62911496-62911496 - TCGA-A5-A0VQ-01 COSM1028983 c.2688G>A p.P896P Substitution - coding silent 20:62894079-62894079 - TCGA-06-0877-01 COSM2152146 c.253G>A p.G85S Substitution - Missense 20:62911360-62911360 - TCGA-BR-6852-01 COSM4100181 c.4551G>T p.S1517S Substitution - coding silent 20:62881405-62881405 - TCGA-Q1-A6DT-01 COSM4850748 c.4480G>C p.E1494Q Substitution - Missense 20:62881476-62881476 - Gp5D COSM2931348 c.210C>T p.R70R Substitution - coding silent 20:62911403-62911403 - Pat_41_A COSM4100221 c.457G>A p.D153N Substitution - Missense 20:62911156-62911156 - PTC-10C COSM127803 c.1740A>C p.T580T Substitution - coding silent 20:62896845-62896845 - LUAD_E01086 COSM354759 c.239T>G p.I80S Substitution - Missense 20:62911374-62911374 - HCA46 COSM4629415 c.2481G>A p.A827A Substitution - coding silent 20:62894504-62894504 - TCGA-18-3414-01 COSM724829 c.2713G>A p.E905K Substitution - Missense 20:62894054-62894054 - TCGA-BG-A0MQ-01 COSM1029001 c.172G>T p.G58C Substitution - Missense 20:62911441-62911441 - T388 COSM4677506 c.4126C>G p.L1376V Substitution - Missense 20:62881830-62881830 - LUAD_E01047 COSM390189 c.483G>C p.L161F Substitution - Missense 20:62911130-62911130 - TCGA-AP-A051-01 COSM1028985 c.2319G>C p.R773S Substitution - Missense 20:62895061-62895061 - HCT8 COSM4624315 c.175C>T p.L59L Substitution - coding silent 20:62911438-62911438 - ESCC_109 COSM5639026 c.4428G>C p.Q1476H Substitution - Missense 20:62881528-62881528 - SA069 COSM213213 c.3330G>C p.K1110N Substitution - Missense 20:62892002-62892002 - CRC-16T COSM2931100 c.5018C>T p.P1673L Substitution - Missense 20:62880938-62880938 - TCGA-QB-A6FS-06 COSM3911757 c.6428C>T p.S2143F Substitution - Missense 20:62879528-62879528 - 587228 COSM1203595 c.5533C>T p.R1845C Substitution - Missense 20:62880423-62880423 - UPCI:SCC090 COSM4603233 c.4878_4879insC p.A1627fs*53 Insertion - Frameshift 20:62881077-62881078 - TCGA-AP-A059-01 COSM1028991 c.1802C>T p.S601F Substitution - Missense 20:62896783-62896783 - TCGA-HU-A4H3-01 COSM2931064 c.6161C>T p.A2054V Substitution - Missense 20:62879795-62879795 - PS-286-7D COSM4423933 c.6122G>T p.W2041L Substitution - Missense 20:62879834-62879834 - TCGA-G4-6586-01 COSM2931339 c.248G>A p.R83H Substitution - Missense 20:62911365-62911365 - T3174 COSM4677516 c.1815G>A p.S605S Substitution - coding silent 20:62896770-62896770 - TCGA-D3-A5GO-06 COSM3548825 c.88C>T p.R30* Substitution - Nonsense 20:62911525-62911525 - TCGA-AP-A0LH-01 COSM1028964 c.6248_6249insT p.E2084fs*9 Insertion - Frameshift 20:62879707-62879708 - 2492722 COSM5723153 c.6713C>T p.S2238L Substitution - Missense 20:62879243-62879243 - GC8_T COSM149206 c.2436G>A p.E812E Substitution - coding silent 20:62894810-62894810 - TCGA-BR-8361-01 COSM4100183 c.4449C>T p.N1483N Substitution - coding silent 20:62881507-62881507 - ESO-859 COSM1238675 c.4771C>T p.P1591S Substitution - Missense 20:62881185-62881185 - TCGA-BR-8077-01 COSM4100221 c.457G>A p.D153N Substitution - Missense 20:62911156-62911156 - cSCCP4 COSM143550 c.5413_5414GG>AA p.G1805K Substitution - Missense 20:62880542-62880543 - TCGA-CM-6161-01 COSM1413008 c.6066C>T p.G2022G Substitution - coding silent 20:62879890-62879890 - UM-SCC-2 COSM4293948 c.4924A>C p.T1642P Substitution - Missense 20:62881032-62881032 - WSU-HN6 COSM4293948 c.4924A>C p.T1642P Substitution - Missense 20:62881032-62881032 - 8030137 COSM3389888 c.3286A>T p.R1096W Substitution - Missense 20:62892046-62892046 - TCGA-AP-A059-01 COSM1028969 c.5190C>T p.G1730G Substitution - coding silent 20:62880766-62880766 - CHEWS003 COSM4581964 c.133G>T p.A45S Substitution - Missense 20:62911480-62911480 - TCGA-CD-8534-01 COSM4100186 c.4325A>T p.D1442V Substitution - Missense 20:62881631-62881631 - TCGA-G3-A6UC-01 COSM4929842 c.2573-2A>T p.? Unknown 20:62894196-62894196 - TCGA-85-6561-01 COSM724843 c.5611G>A p.E1871K Substitution - Missense 20:62880345-62880345 - TCGA-AA-3713-01 COSM1413016 c.3938C>T p.P1313L Substitution - Missense 20:62882018-62882018 - BD124T COSM5494120 c.4394C>T p.A1465V Substitution - Missense 20:62881562-62881562 - 2334191 COSM319882 c.3750C>G p.D1250E Substitution - Missense 20:62882206-62882206 - T2957 COSM4677498 c.5998G>A p.E2000K Substitution - Missense 20:62879958-62879958 - TCGA-A8-A07R-01 COSM3841463 c.4152A>G p.P1384P Substitution - coding silent 20:62881804-62881804 - TCGA-BR-A4QI-01 COSM4100180 c.4685A>T p.Q1562L Substitution - Missense 20:62881271-62881271 - TCGA-FW-A3R5-06 COSM3911760 c.4089C>T p.I1363I Substitution - coding silent 20:62881867-62881867 - HCA46 COSM4611936 c.1715_1717delCTT p.S572delS Deletion - In frame 20:62896868-62896870 - TCGA-CM-6171-01 COSM1413034 c.686C>T p.A229V Substitution - Missense 20:62910927-62910927 - T3535 COSM4440603 c.6101delC p.P2034fs*>207 Deletion - Frameshift 20:62879855-62879855 - 1_PRE-TREATMENT COSM1718608 c.6046C>T p.P2016S Substitution - Missense 20:62879910-62879910 - LUAD-RT-S01702 COSM379270 c.663C>T p.N221N Substitution - coding silent 20:62910950-62910950 - LIM1899 COSM4640292 c.5056C>T p.P1686S Substitution - Missense 20:62880900-62880900 - pfg057T COSM4756275 c.1046A>T p.D349V Substitution - Missense 20:62909814-62909814 - TCGA-EK-A3GK-01 COSM4853950 c.3101+2T>A p.? Unknown 20:62893664-62893664 - CSCC-62-T COSM4484713 c.2842C>T p.P948S Substitution - Missense 20:62893925-62893925 - T3503 COSM4677502 c.4897G>A p.G1633S Substitution - Missense 20:62881059-62881059 - PD4596a COSM160429 c.2327G>A p.R776K Substitution - Missense 20:62895053-62895053 - TCGA-CH-5750-01 COSM1130582 c.2892C>T p.S964S Substitution - coding silent 20:62893875-62893875 - T3147 COSM4677525 c.732G>A p.Q244Q Substitution - coding silent 20:62910881-62910881 - LIM2405 COSM4642455 c.6146C>T p.A2049V Substitution - Missense 20:62879810-62879810 - CSCC-7-T COSM109496 c.3989C>T p.P1330L Substitution - Missense 20:62881967-62881967 - YUKAT COSM5392549 c.3905C>T p.S1302F Substitution - Missense 20:62882051-62882051 - ME029T COSM226848 c.5500C>T p.P1834S Substitution - Missense 20:62880456-62880456 - C086 COSM5529735 c.4766C>T p.A1589V Substitution - Missense 20:62881190-62881190 - TCGA-AP-A0LM-01 COSM1028982 c.2969A>G p.H990R Substitution - Missense 20:62893798-62893798 - Pat_59_A COSM5858301 c.6126_6127GG>AA p.E2043K Substitution - Missense 20:62879829-62879830 - ORL-48 COSM4293948 c.4924A>C p.T1642P Substitution - Missense 20:62881032-62881032 - CHOL11 COSM1743166 c.5161G>C p.G1721R Substitution - Missense 20:62880795-62880795 - sysucc-1163T COSM5458847 c.5065G>A p.A1689T Substitution - Missense 20:62880891-62880891 - LUAD-E00897 COSM364558 c.3957G>A p.Q1319Q Substitution - coding silent 20:62881999-62881999 - TCGA-AO-A128-01 COSM3841477 c.403C>T p.R135* Substitution - Nonsense 20:62911210-62911210 - OSCC-GB_01060111 COSM4883102 c.5810C>A p.A1937D Substitution - Missense 20:62880146-62880146 - ESCC_BICR_048T COSM5432350 c.3669G>A p.A1223A Substitution - coding silent 20:62882287-62882287 - TCGA-AA-A010-01 COSM280387 c.1412C>A p.A471D Substitution - Missense 20:62906063-62906063 - YUGASP COSM1713784 c.3082C>T p.P1028S Substitution - Missense 20:62893685-62893685 - Pat_59_B COSM5858301 c.6126_6127GG>AA p.E2043K Substitution - Missense 20:62879829-62879830 - TCGA-AA-3516-01 COSM291549 c.2938G>A p.A980T Substitution - Missense 20:62893829-62893829 - ESCC_BICR_054T COSM5444257 c.345G>A p.V115V Substitution - coding silent 20:62911268-62911268 - S02194 COSM5674883 c.3724T>C p.S1242P Substitution - Missense 20:62882232-62882232 - Pat_24_A COSM5858306 c.3361C>T p.R1121C Substitution - Missense 20:62891140-62891140 - PD9467a COSM5800238 c.5148A>C p.A1716A Substitution - coding silent 20:62880808-62880808 - TCGA-DR-A0ZM-01 COSM459705 c.5700G>C p.L1900L Substitution - coding silent 20:62880256-62880256 - 12-P616 COSM4581968 c.11A>T p.K4I Substitution - Missense 20:62911602-62911602 - TCGA-C5-A1MF-01 COSM4820745 c.2071G>C p.D691H Substitution - Missense 20:62896376-62896376 - TCGA-D1-A103-01 COSM1029000 c.184C>T p.R62W Substitution - Missense 20:62911429-62911429 - TCGA-FW-A3R5-06 COSM3911767 c.590C>T p.P197L Substitution - Missense 20:62911023-62911023 - T96 COSM4677503 c.4693C>T p.R1565C Substitution - Missense 20:62881263-62881263 - TCGA-13-1512-01 COSM115803 c.5435C>T p.S1812L Substitution - Missense 20:62880521-62880521 - NB-1931 COSM1284496 c.5200G>T p.A1734S Substitution - Missense 20:62880756-62880756 - T3225 COSM4677499 c.5591C>T p.T1864M Substitution - Missense 20:62880365-62880365 - PTC-46C COSM4134751 c.4691G>T p.R1564M Substitution - Missense 20:62881265-62881265 - T1772 COSM4677521 c.859C>T p.R287C Substitution - Missense 20:62910001-62910001 - ESCC_BICR_063T COSM5436962 c.1625C>A p.A542E Substitution - Missense 20:62896960-62896960 - TCGA-DA-A1I0-06 COSM1713786 c.1702C>T p.P568S Substitution - Missense 20:62896883-62896883 - pfg106T COSM4756269 c.6490G>A p.D2164N Substitution - Missense 20:62879466-62879466 - WSU-HN30 COSM4603233 c.4878_4879insC p.A1627fs*53 Insertion - Frameshift 20:62881077-62881078 - C658 COSM4443425 c.3373G>A p.A1125T Substitution - Missense 20:62891128-62891128 - TCGA-EJ-A46G-01 COSM3783507 c.2877C>T p.T959T Substitution - coding silent 20:62893890-62893890 - B104 COSM1751550 c.1863A>G p.A621A Substitution - coding silent 20:62896722-62896722 - TCGA-06-0877 COSM2152146 c.253G>A p.G85S Substitution - Missense 20:62911360-62911360 - ESCC_151 COSM5645211 c.3420C>T p.F1140F Substitution - coding silent 20:62891081-62891081 - OSCC-GB_00810111 COSM4891264 c.6297G>T p.P2099P Substitution - coding silent 20:62879659-62879659 - CHC892T COSM4958552 c.1478G>A p.G493E Substitution - Missense 20:62905997-62905997 - BCM723T COSM4950262 c.2612_2613insA p.Q872fs*8 Insertion - Frameshift 20:62894154-62894155 - TCGA-EM-A2CL-01 COSM3371749 c.5019G>C p.P1673P Substitution - coding silent 20:62880937-62880937 - TCGA-AA-3821-01 COSM294309 c.4153T>C p.Y1385H Substitution - Missense 20:62881803-62881803 - WSU-HN8 COSM4591406 c.4867G>A p.E1623K Substitution - Missense 20:62881089-62881089 - TCGA-HU-A4GQ-01 COSM4100229 c.219C>T p.R73R Substitution - coding silent 20:62911394-62911394 - 185T COSM4383131 c.2650A>T p.K884* Substitution - Nonsense 20:62894117-62894117 - TCGA-AA-A010-01 COSM280385 c.3530T>G p.F1177C Substitution - Missense 20:62890971-62890971 - 1_RESISTANT COSM1718608 c.6046C>T p.P2016S Substitution - Missense 20:62879910-62879910 - TCGA-A7-A0D9-01 COSM444192 c.483G>A p.L161L Substitution - coding silent 20:62911130-62911130 - TCGA-FP-A4BF-01 COSM4100201 c.1477G>A p.G493R Substitution - Missense 20:62905998-62905998 - TCGA-B5-A11R-01 COSM1028963 c.6579G>A p.R2193R Substitution - coding silent 20:62879377-62879377 - TCGA-HU-8602-01 COSM4100209 c.878A>G p.H293R Substitution - Missense 20:62909982-62909982 - BN45 COSM1615832 c.3116G>T p.R1039L Substitution - Missense 20:62892948-62892948 - TCGA-AA-3713-01 COSM1172738 c.6596G>A p.R2199Q Substitution - Missense 20:62879360-62879360 - TCGA-D1-A103-01 COSM1028977 c.3980C>A p.S1327* Substitution - Nonsense 20:62881976-62881976 - PTC-77C COSM127803 c.1740A>C p.T580T Substitution - coding silent 20:62896845-62896845 - TCGA-BR-8360-01 COSM1615833 c.2536G>T p.A846S Substitution - Missense 20:62894449-62894449 - OSCC-GB_00560111 COSM4883561 c.774G>T p.K258N Substitution - Missense 20:62910839-62910839 - TCGA-HU-A4GQ-01 COSM2931339 c.248G>A p.R83H Substitution - Missense 20:62911365-62911365 - TCGA-GN-A266-06 COSM3548792 c.3779C>T p.S1260L Substitution - Missense 20:62882177-62882177 - TCGA-BR-4201-01 COSM4100195 c.2534G>A p.R845H Substitution - Missense 20:62894451-62894451 - T3064 COSM4677537 c.338_339insG p.S114fs*7 Insertion - Frameshift 20:62911274-62911275 - ESCC_168 COSM5648768 c.1759C>T p.P587S Substitution - Missense 20:62896826-62896826 - TCGA-DK-A3IT-01 COSM1307616 c.901G>A p.E301K Substitution - Missense 20:62909959-62909959 - TCGA-AP-A0LM-01 COSM1028979 c.3541+6C>T p.? Unknown 20:62890954-62890954 - YUFERY COSM5392550 c.3571C>T p.L1191F Substitution - Missense 20:62882385-62882385 - TCGA-66-2767-01 COSM724831 c.3439G>T p.G1147C Substitution - Missense 20:62891062-62891062 - SNUH_G26_S1 COSM3681227 c.6206A>C p.D2069A Substitution - Missense 20:62879750-62879750 - TCGA-IP-7968-01 COSM4100189 c.3911C>T p.A1304V Substitution - Missense 20:62882045-62882045 - WSU-HN6 COSM4603233 c.4878_4879insC p.A1627fs*53 Insertion - Frameshift 20:62881077-62881078 - T263 COSM1028981 c.3218C>T p.A1073V Substitution - Missense 20:62892846-62892846 - TCGA-AC-A23H-01 COSM3841473 c.784G>A p.E262K Substitution - Missense 20:62910829-62910829 - HCA46 COSM4611940 c.1712_1713delCT p.S571fs*4 Deletion - Frameshift 20:62896872-62896873 - 3N46-VS-3T46 COSM4982519 c.4509G>C p.Q1503H Substitution - Missense 20:62881447-62881447 - TCGA-EA-A439-01 COSM4843656 c.6127G>A p.E2043K Substitution - Missense 20:62879829-62879829 - T3498 COSM1413012 c.5379A>G p.R1793R Substitution - coding silent 20:62880577-62880577 - PD4226a COSM160428 c.4258G>A p.E1420K Substitution - Missense 20:62881698-62881698 - CSCC-45-T COSM4517603 c.3813_3814GG>AA p.V1272M Substitution - Missense 20:62882142-62882143 - PCSI_0048_Pa_P_526 COSM216496 c.2647T>C p.L883L Substitution - coding silent 20:62894120-62894120 - CSCC-31-T COSM2931068 c.6088C>T p.P2030S Substitution - Missense 20:62879868-62879868 - TCGA-EE-A2MR-06 COSM1028965 c.5901C>T p.F1967F Substitution - coding silent 20:62880055-62880055 - PTC-7C COSM3758729 c.4702A>G p.T1568A Substitution - Missense 20:62881254-62881254 - CSCC-16-T COSM4557218 c.719G>A p.G240E Substitution - Missense 20:62910894-62910894 - PT48 COSM5934003 c.5246C>T p.P1749L Substitution - Missense 20:62880710-62880710 - STC248 COSM5057489 c.4257C>T p.A1419A Substitution - coding silent 20:62881699-62881699 - T2991 COSM1723061 c.4927_4928insC p.R1643fs*37 Insertion - Frameshift 20:62881028-62881029 - MCF7 COSM1681830 c.4167G>T p.E1389D Substitution - Missense 20:62881789-62881789 - ESO-0115 COSM1250073 c.5372G>C p.G1791A Substitution - Missense 20:62880584-62880584 - TCGA-EE-A2MS-06 COSM3548788 c.4024C>T p.L1342F Substitution - Missense 20:62881932-62881932 - WSU-HN12 COSM4591406 c.4867G>A p.E1623K Substitution - Missense 20:62881089-62881089 - HCT15 COSM4624313 c.3751G>A p.A1251T Substitution - Missense 20:62882205-62882205 - PT08_1 COSM5894078 c.4072C>T p.P1358S Substitution - Missense 20:62881884-62881884 - LUAD-B00523 COSM331949 c.3660G>T p.P1220P Substitution - coding silent 20:62882296-62882296 - CRC-03T COSM5451588 c.4211G>A p.R1404Q Substitution - Missense 20:62881745-62881745 - TCGA-GF-A6C9-06 COSM1534249 c.5869C>T p.P1957S Substitution - Missense 20:62880087-62880087 - TCGA-EE-A3JD-06 COSM1028986 c.2176C>T p.R726C Substitution - Missense 20:62896271-62896271 - T3080 COSM4624313 c.3751G>A p.A1251T Substitution - Missense 20:62882205-62882205 - HCC009T COSM5819862 c.4881G>T p.A1627A Substitution - coding silent 20:62881075-62881075 - SCC-25 COSM4603233 c.4878_4879insC p.A1627fs*53 Insertion - Frameshift 20:62881077-62881078 - PTC-14C COSM4134752 c.2669C>G p.S890C Substitution - Missense 20:62894098-62894098 - T578 COSM4677497 c.6249C>T p.F2083F Substitution - coding silent 20:62879707-62879707 - TCGA-D5-6930-01 COSM1413006 c.6349C>T p.R2117C Substitution - Missense 20:62879607-62879607 - ESO-085 COSM1250076 c.5414G>A p.G1805E Substitution - Missense 20:62880542-62880542 - BD165T COSM5506013 c.4387C>T p.P1463S Substitution - Missense 20:62881569-62881569 - TCGA-46-3767-01 COSM724822 c.1086A>C p.E362D Substitution - Missense 20:62909774-62909774 - TCGA-ED-A4XI-01 COSM4913154 c.5487T>C p.S1829S Substitution - coding silent 20:62880469-62880469 - CA2 COSM1166149 c.6357C>T p.R2119R Substitution - coding silent 20:62879599-62879599 - TCGA-BH-A0WA-01 COSM444187 c.4572A>C p.P1524P Substitution - coding silent 20:62881384-62881384 - TCGA-70-6722-01 COSM724833 c.3645G>A p.R1215R Substitution - coding silent 20:62882311-62882311 - TCGA-AA-3510-01 COSM1413019 c.3332C>T p.S1111F Substitution - Missense 20:62892000-62892000 - TCGA-HU-A4HD-01 COSM4100178 c.5247G>A p.P1749P Substitution - coding silent 20:62880709-62880709 - 1N62-VS-1T62 COSM4977894 c.2316G>C p.E772D Substitution - Missense 20:62895064-62895064 - PT52 COSM5930010 c.6143C>T p.S2048F Substitution - Missense 20:62879813-62879813 - ESCC_BICR_051T COSM5444039 c.1326G>C p.K442N Substitution - Missense 20:62907195-62907195 - TCGA-EM-A22J-01 COSM260420 c.3154C>T p.R1052* Substitution - Nonsense 20:62892910-62892910 - TCGA-70-6722-01 COSM724825 c.1860G>T p.A620A Substitution - coding silent 20:62896725-62896725 - 2492720 COSM5723153 c.6713C>T p.S2238L Substitution - Missense 20:62879243-62879243 - PTC_171 COSM1723061 c.4927_4928insC p.R1643fs*37 Insertion - Frameshift 20:62881028-62881029 - CSCC-62-T COSM4499064 c.5338C>T p.P1780S Substitution - Missense 20:62880618-62880618 - PCSI_0083_Pa_X COSM3379109 c.2067C>T p.S689S Substitution - coding silent 20:62896380-62896380 - LUAD-NYU195 COSM371126 c.1145T>G p.L382R Substitution - Missense 20:62909715-62909715 - TCGA-EE-A20C-06 COSM3548783 c.4787C>T p.S1596F Substitution - Missense 20:62881169-62881169 - sysucc-1370T COSM5471246 c.160C>T p.Q54* Substitution - Nonsense 20:62911453-62911453 - 587228 COSM1203596 c.110G>A p.R37Q Substitution - Missense 20:62911503-62911503 - TCGA-EE-A29V-06 COSM3423807 c.3914C>T p.S1305L Substitution - Missense 20:62882042-62882042 - CHC1207T COSM4800152 c.2959G>C p.D987H Substitution - Missense 20:62893808-62893808 - TCGA-AA-A01K-01 COSM301526 c.2755_2756GC>AT p.A919>? Complex 20:62894011-62894012 - Pat_24_B COSM5858302 c.5875C>T p.P1959S Substitution - Missense 20:62880081-62880081 - LC_C4 COSM1190306 c.5548G>T p.G1850W Substitution - Missense 20:62880408-62880408 - CSCC-16-T COSM4551900 c.543G>A p.L181L Substitution - coding silent 20:62911070-62911070 - LUAD-F00057 COSM339410 c.5054G>T p.C1685F Substitution - Missense 20:62880902-62880902 - SC_9047 COSM5554470 c.3432C>T p.G1144G Substitution - coding silent 20:62891069-62891069 - CSCC-49-T COSM4491038 c.3733C>T p.P1245S Substitution - Missense 20:62882223-62882223 - ESO-1133 COSM1250077 c.4618C>T p.Q1540* Substitution - Nonsense 20:62881338-62881338 - BCM723T COSM4950262 c.2612_2613insA p.Q872fs*8 Insertion - Frameshift 20:62894154-62894155 - PTC_72 COSM5959645 c.2499C>T p.F833F Substitution - coding silent 20:62894486-62894486 - DU-145 COSM1681835 c.436G>T p.D146Y Substitution - Missense 20:62911177-62911177 - MO_1012 COSM5547503 c.1200delC p.C402fs*25 Deletion - Frameshift 20:62907321-62907321 - KYSE-510 COSM2931110 c.4544C>T p.S1515L Substitution - Missense 20:62881412-62881412 - KM12 COSM2931133 c.3738C>T p.L1246L Substitution - coding silent 20:62882218-62882218 - sysucc-274T COSM1166149 c.6357C>T p.R2119R Substitution - coding silent 20:62879599-62879599 - TCGA-24-1422-01 COSM133407 c.3610_3611AA>GC p.N1204A Substitution - Missense 20:62882345-62882346 - 2492721 COSM5723153 c.6713C>T p.S2238L Substitution - Missense 20:62879243-62879243 - CSCC-52-T COSM4496891 c.4850C>T p.S1617F Substitution - Missense 20:62881106-62881106 - BD236T COSM5519754 c.2237G>A p.R746H Substitution - Missense 20:62895143-62895143 - TCGA-A6-6653-01 COSM1413023 c.2133delT p.F711fs*22 Deletion - Frameshift 20:62896314-62896314 - TCGA-59-2354-01 COSM118758 c.4056C>T p.D1352D Substitution - coding silent 20:62881900-62881900 - PTC-70C COSM127803 c.1740A>C p.T580T Substitution - coding silent 20:62896845-62896845 - PD4203a COSM160426 c.908G>A p.R303Q Substitution - Missense 20:62909952-62909952 - TCGA-A7-A0D9-01 COSM444191 c.697G>A p.D233N Substitution - Missense 20:62910916-62910916 - YUKLAB COSM1713783 c.3488C>T p.P1163L Substitution - Missense 20:62891013-62891013 - PTC-46C COSM127803 c.1740A>C p.T580T Substitution - coding silent 20:62896845-62896845 - TCGA-CK-5916-01 COSM3693703 c.1224C>T p.P408P Substitution - coding silent 20:62907297-62907297 - LIM1215 COSM4639470 c.6523C>A p.R2175R Substitution - coding silent 20:62879433-62879433 - LUAD-CHTN-Z4716A COSM362143 c.6666G>T p.R2222R Substitution - coding silent 20:62879290-62879290 - LUAD-QCHM7 COSM377224 c.4441G>T p.E1481* Substitution - Nonsense 20:62881515-62881515 - LUAD-5V8LT COSM402221 c.1839G>T p.Q613H Substitution - Missense 20:62896746-62896746 - SS6003317 COSM4019734 c.4548G>T p.V1516V Substitution - coding silent 20:62881408-62881408 - HCC157T COSM3707918 c.3204A>G p.K1068K Substitution - coding silent 20:62892860-62892860 - PCSI0048 COSM216496 c.2647T>C p.L883L Substitution - coding silent 20:62894120-62894120 - TCGA-EE-A2MJ-06 COSM1130582 c.2892C>T p.S964S Substitution - coding silent 20:62893875-62893875 - SE2 COSM1165740 c.4795G>T p.G1599C Substitution - Missense 20:62881161-62881161 - BN37T COSM1615833 c.2536G>T p.A846S Substitution - Missense 20:62894449-62894449 - I2L-P19Tb-Tumor-Organoid COSM5365808 c.6497delG p.G2166fs*>75 Deletion - Frameshift 20:62879459-62879459 - TCGA-BS-A0UJ-01 COSM1029002 c.25A>G p.N9D Substitution - Missense 20:62911588-62911588 - 587220 COSM1203593 c.6512G>A p.R2171H Substitution - Missense 20:62879444-62879444 - YUKLAB COSM1713781 c.4220G>A p.R1407H Substitution - Missense 20:62881736-62881736 - ESO-1481 COSM1250082 c.6376G>A p.E2126K Substitution - Missense 20:62879580-62879580 - TCGA-EE-A2A0-06 COSM3548778 c.5308A>G p.N1770D Substitution - Missense 20:62880648-62880648 - BICR_22 COSM4591406 c.4867G>A p.E1623K Substitution - Missense 20:62881089-62881089 - 93VU147T COSM4603233 c.4878_4879insC p.A1627fs*53 Insertion - Frameshift 20:62881077-62881078 - B77 COSM1757016 c.3809C>T p.P1270L Substitution - Missense 20:62882147-62882147 - T469 COSM4677497 c.6249C>T p.F2083F Substitution - coding silent 20:62879707-62879707 - ESO-120 COSM1250080 c.523G>A p.E175K Substitution - Missense 20:62911090-62911090 - TCGA-CD-A4MG-01 COSM4100184 c.4430A>C p.K1477T Substitution - Missense 20:62881526-62881526 - C008 COSM5522499 c.4815C>T p.P1605P Substitution - coding silent 20:62881141-62881141 - B81-2 COSM1757015 c.4470G>C p.K1490N Substitution - Missense 20:62881486-62881486 - TCGA-FW-A3R5-06 COSM3548770 c.6020C>T p.S2007L Substitution - Missense 20:62879936-62879936 - TCGA-33-4566-01 COSM724832 c.3534G>T p.E1178D Substitution - Missense 20:62890967-62890967 - TCGA-D9-A149-06 COSM3548782 c.4847C>T p.S1616F Substitution - Missense 20:62881109-62881109 - T3454 COSM2931107 c.4711G>A p.G1571S Substitution - Missense 20:62881245-62881245 - SC_9047 COSM5569434 c.6244A>T p.T2082S Substitution - Missense 20:62879712-62879712 - CSCC-7-T COSM4500921 c.5769C>T p.F1923F Substitution - coding silent 20:62880187-62880187 - TCGA-CK-5915-01 COSM1413020 c.2507T>C p.M836T Substitution - Missense 20:62894478-62894478 - TCGA-DK-A3IK-01 COSM1307611 c.3776G>T p.G1259V Substitution - Missense 20:62882180-62882180 - TCGA-EE-A29S-06 COSM3548785 c.4368C>T p.S1456S Substitution - coding silent 20:62881588-62881588 - TCGA-AA-3662-01 COSM3758729 c.4702A>G p.T1568A Substitution - Missense 20:62881254-62881254 - cSCCP4 COSM139202 c.332C>T p.S111F Substitution - Missense 20:62911281-62911281 - KYSE-450 COSM2931126 c.3999A>G p.R1333R Substitution - coding silent 20:62881957-62881957 - TCGA-D9-A3Z1-06 COSM3548787 c.4044C>T p.T1348T Substitution - coding silent 20:62881912-62881912 - PTC-7C COSM4134755 c.1272G>A p.A424A Substitution - coding silent 20:62907249-62907249 - T3064 COSM4677505 c.4407G>A p.T1469T Substitution - coding silent 20:62881549-62881549 - TCGA-AA-3715-01 COSM269013 c.633C>T p.G211G Substitution - coding silent 20:62910980-62910980 - TCGA-FV-A3R3-01 COSM4921898 c.5596G>A p.A1866T Substitution - Missense 20:62880360-62880360 - TCGA-B2-4102-01 COSM1136807 c.5423C>T p.P1808L Substitution - Missense 20:62880533-62880533 - TCGA-EI-6883-01 COSM3423806 c.5440C>T p.Q1814* Substitution - Nonsense 20:62880516-62880516 - TCGA-A2-A0YG-01 COSM444188 c.4516G>A p.A1506T Substitution - Missense 20:62881440-62881440 - WSU-HN13 COSM4603233 c.4878_4879insC p.A1627fs*53 Insertion - Frameshift 20:62881077-62881078 - TCGA-AX-A05Z-01 COSM1028998 c.907C>T p.R303* Substitution - Nonsense 20:62909953-62909953 - PTC-1C COSM127803 c.1740A>C p.T580T Substitution - coding silent 20:62896845-62896845 - PD9000a COSM5775643 c.399G>A p.K133K Substitution - coding silent 20:62911214-62911214 - TCGA-G2-A2EC-01 COSM1307609 c.4330C>T p.L1444L Substitution - coding silent 20:62881626-62881626 - ORL-48 COSM4603233 c.4878_4879insC p.A1627fs*53 Insertion - Frameshift 20:62881077-62881078 - T3024 COSM4677501 c.5023C>T p.Q1675* Substitution - Nonsense 20:62880933-62880933 - B77-Tumor COSM1757016 c.3809C>T p.P1270L Substitution - Missense 20:62882147-62882147 - YUFERY COSM1713785 c.2914C>T p.P972S Substitution - Missense 20:62893853-62893853 - TCGA-ER-A19N-06 COSM3548821 c.440A>G p.D147G Substitution - Missense 20:62911173-62911173 - TCGA-EE-A2GC-06 COSM3548774 c.5544C>T p.P1848P Substitution - coding silent 20:62880412-62880412 - RK119_C01 COSM3740223 c.2865C>T p.S955S Substitution - coding silent 20:62893902-62893902 - T3182 COSM4677533 c.469G>A p.D157N Substitution - Missense 20:62911144-62911144 - SC_9099 COSM5551701 c.5165A>G p.D1722G Substitution - Missense 20:62880791-62880791 - TCGA-66-2773-01 COSM724841 c.5299C>T p.H1767Y Substitution - Missense 20:62880657-62880657 - ESCC_95 COSM5637511 c.6590G>A p.R2197Q Substitution - Missense 20:62879366-62879366 - LC_C9 COSM1190308 c.1136A>T p.K379M Substitution - Missense 20:62909724-62909724 - HCC18T COSM1615831 c.5010C>T p.P1670P Substitution - coding silent 20:62880946-62880946 - MD-343 COSM302054 c.6228C>T p.H2076H Substitution - coding silent 20:62879728-62879728 - sysucc-274T COSM5476192 c.3750C>T p.D1250D Substitution - coding silent 20:62882206-62882206 - CAL33 COSM4591407 c.4872G>C p.K1624N Substitution - Missense 20:62881084-62881084 - OVCAR-4 COSM1681833 c.3505C>A p.P1169T Substitution - Missense 20:62890996-62890996 - PT52 COSM5941007 c.1783C>T p.P595S Substitution - Missense 20:62896802-62896802 - TCGA-22-4599-01 COSM724828 c.2630C>T p.S877F Substitution - Missense 20:62894137-62894137 - LC_C23 COSM1190307 c.4061T>G p.V1354G Substitution - Missense 20:62881895-62881895 - CSCC-7-T COSM4500882 c.5758C>T p.P1920S Substitution - Missense 20:62880198-62880198 -

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.517172 20q13.33 604140

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A C Missense p.L1161R c.3482T>G 20 61522371 BRCA - A Frameshift p.E2084Rfs*9 c.6248dupT 20 61511060 UCEC A G Missense p.L213P c.638T>C 20 61542327 CM A G Synonymous p.L767L c.2301T>C 20 61526431 RCCC A G Synonymous p.L883L c.2647T>C 20 61525472 PAAD A - IntronicDeletion . c.3102-18delT 20 61524332 STAD A T Missense p.W1103R c.3307T>A 20 61523377 BRCA C A Missense p.A1734S c.5200G>T 20 61512108 NB C A Missense p.A422S c.1264G>T 20 61538609 STAD C A Missense p.D1373Y c.4117G>T 20 61513191 LUSC C A Missense p.D363Y c.1087G>T 20 61541125 ESCA C A Missense p.G1147C c.3439G>T 20 61522414 LUSC C A Missense p.G1259V c.3776G>T 20 61513532 BLCA C A Missense p.G158V c.473G>T 20 61542492 LUAD C A Missense p.G1883V c.5648G>T 20 61511660 COREAD C A Missense p.G554C c.1660G>T 20 61528277 LUAD C A Missense p.G58C c.172G>T 20 61542793 UCEC C A Missense p.Q1803H c.5409G>T 20 61511899 BRCA C A Missense p.Q217H c.651G>T 20 61542314 LUAD C A Missense p.R193L c.578G>T 20 61542387 CM C A Missense p.R2145L c.6434G>T 20 61510874 STAD C A Nonsense p.E108* c.322G>T 20 61542643 LUAD C A Nonsense p.E1409* c.4225G>T 20 61513083 LUAD C A Synonymous p.A620A c.1860G>T 20 61528077 LUSC C A Synonymous p.L1314L c.3942G>T 20 61513366 LUAD C A Synonymous p.S1517S c.4551G>T 20 61512757 STAD C A Synonymous p.T332T c.996G>T 20 61541216 LUAD C A Synonymous p.T622T c.1866G>T 20 61528071 UCEC C G Missense p.D2092H c.6274G>C 20 61511034 HNSC C G Missense p.D346H c.1036G>C 20 61541176 HNSC C G Missense p.D897H c.2689G>C 20 61525430 LUAD C G Missense p.E1411Q c.4231G>C 20 61513077 LUAD C G Missense p.E747Q c.2239G>C 20 61526493 BLCA C G Missense p.G1791A c.5372G>C 20 61511936 ESCA C G Missense p.K1110N c.3330G>C 20 61523354 BRCA C G Missense p.Q2081H c.6243G>C 20 61511065 HNSC C G Missense p.R1412S c.4236G>C 20 61513072 BLCA C G Missense p.R1775T c.5324G>C 20 61511984 LUAD C G Missense p.R1824T c.5471G>C 20 61511837 BLCA C G SpliceAcceptorSNV . c.2055-1G>C 20 61527745 HNSC C G SpliceDonorSNV . c.3345+1G>C 20 61523338 BRCA C G Synonymous p.A1294A c.3882G>C 20 61513426 CM C G Synonymous p.P1673P c.5019G>C 20 61512289 THCA C T IntronicSNV . c.3541+3481G>A 20 61518831 HC C T Missense p.A1506T c.4516G>A 20 61512792 BRCA C T Missense p.A15T c.43G>A 20 61542922 HNSC C T Missense p.A1787T c.5359G>A 20 61511949 CM C T Missense p.A423T c.1267G>A 20 61538606 STAD C T Missense p.A602T c.1804G>A 20 61528133 STAD C T Missense p.A614T c.1840G>A 20 61528097 HNSC C T Missense p.D1021N c.3061G>A 20 61525058 HNSC C T Missense p.D222N c.664G>A 20 61542301 THCA C T Missense p.D233N c.697G>A 20 61542268 BRCA C T Missense p.D416N c.1246G>A 20 61538627 OV C T Missense p.D987N c.2959G>A 20 61525160 HNSC C T Missense p.E116K c.346G>A 20 61542619 HNSC C T Missense p.E1238K c.3712G>A 20 61513596 CM C T Missense p.E1378K c.4132G>A 20 61513176 LUAD C T Missense p.E1394K c.4180G>A 20 61513128 STAD C T Missense p.E1420K c.4258G>A 20 61513050 BRCA C T Missense p.E1420K c.4258G>A 20 61513050 STAD C T Missense p.E1592K c.4774G>A 20 61512534 HNSC C T Missense p.E1720K c.5158G>A 20 61512150 BLCA C T Missense p.E175K c.523G>A 20 61542442 ESCA C T Missense p.E1871K c.5611G>A 20 61511697 LUSC C T Missense p.E2118K c.6352G>A 20 61510956 BRCA C T Missense p.E2126K c.6376G>A 20 61510932 ESCA C T Missense p.E301K c.901G>A 20 61541311 BLCA C T Missense p.E905K c.2713G>A 20 61525406 LUSC C T Missense p.E909K c.2725G>A 20 61525394 CM C T Missense p.G145R c.433G>A 20 61542532 CM C T Missense p.G1678S c.5032G>A 20 61512276 CM C T Missense p.G1801E c.5402G>A 20 61511906 CM C T Missense p.G1805E c.5414G>A 20 61511894 ESCA C T Missense p.G1990D c.5969G>A 20 61511339 LUAD C T Missense p.G630D c.1889G>A 20 61528048 STAD C T Missense p.G85S c.253G>A 20 61542712 GBM C T Missense p.R2040H c.6119G>A 20 61511189 GBM C T Missense p.R2113K c.6338G>A 20 61510970 CM C T Missense p.R2127Q c.6380G>A 20 61510928 CM C T Missense p.R303Q c.908G>A 20 61541304 BRCA C T Missense p.R30Q c.89G>A 20 61542876 CM C T Missense p.R776K c.2327G>A 20 61526405 BRCA C T Missense p.R845H c.2534G>A 20 61525803 STAD C T Missense p.S660N c.1979G>A 20 61527958 OV C T Synonymous p.E1569E c.4707G>A 20 61512601 LUSC C T Synonymous p.E2097E c.6291G>A 20 61511017 CM C T Synonymous p.L161L c.483G>A 20 61542482 BRCA C T Synonymous p.P1187P c.3561G>A 20 61513747 STAD C T Synonymous p.P453P c.1359G>A 20 61538514 ESCA C T Synonymous p.P896P c.2688G>A 20 61525431 UCEC C T Synonymous p.Q1503Q c.4509G>A 20 61512799 BLCA C T Synonymous p.R1215R c.3645G>A 20 61513663 LUSC C T Synonymous p.R2193R c.6579G>A 20 61510729 UCEC C T Synonymous p.R597R c.1791G>A 20 61528146 LUSC C T Synonymous p.S1305S c.3915G>A 20 61513393 CM C T Synonymous p.V388V c.1164G>A 20 61538709 CM G A 3-UTRSNV . c.6720+10C>T 20 61510578 MB G A IntronicSNV . c.1588+27C>T 20 61537212 RCCC G A IntronicSNV . c.3541+3482C>T 20 61518830 HC G A Missense p.A333V c.998C>T 20 61541214 OV G A Missense p.A406V c.1217C>T 20 61538656 UCEC G A Missense p.H1767Y c.5299C>T 20 61512009 LUSC G A Missense p.H509Y c.1525C>T 20 61537302 CM G A Missense p.L1342F c.4024C>T 20 61513284 CM G A Missense p.P1262L c.3785C>T 20 61513523 STAD G A Missense p.P1268S c.3802C>T 20 61513506 CM G A Missense p.P1286L c.3857C>T 20 61513451 CM G A Missense p.P1445S c.4333C>T 20 61512975 UCEC G A Missense p.P1663L c.4988C>T 20 61512320 GBM G A Missense p.P1664S c.4990C>T 20 61512318 LUAD G A Missense p.P1774S c.5320C>T 20 61511988 CM G A Missense p.P1942S c.5824C>T 20 61511484 CM G A Missense p.P1957L c.5870C>T 20 61511438 CM G A Missense p.P2059L c.6176C>T 20 61511132 CM G A Missense p.P453L c.1358C>T 20 61538515 CM G A Missense p.P486S c.1456C>T 20 61537371 CM G A Missense p.P553L c.1658C>T 20 61528279 CM G A Missense p.P568S c.1702C>T 20 61528235 CM G A Missense p.P794S c.2380C>T 20 61526218 CM G A Missense p.P972S c.2914C>T 20 61525205 CM G A Missense p.R726C c.2176C>T 20 61527623 CM G A Missense p.S1011F c.3032C>T 20 61525087 CM G A Missense p.S1040F c.3119C>T 20 61524297 CM G A Missense p.S1305L c.3914C>T 20 61513394 CM G A Missense p.S1471F c.4412C>T 20 61512896 LUSC G A Missense p.S1596F c.4787C>T 20 61512521 CM G A Missense p.S1621L c.4862C>T 20 61512446 BLCA G A Missense p.S1651L c.4952C>T 20 61512356 CM G A Missense p.S1812L c.5435C>T 20 61511873 OV G A Missense p.S1999F c.5996C>T 20 61511312 CM G A Missense p.S2007L c.6020C>T 20 61511288 CM G A Missense p.S504L c.1511C>T 20 61537316 BLCA G A Missense p.S537F c.1610C>T 20 61528327 CM G A Missense p.S645F c.1934C>T 20 61528003 CM G A Missense p.S877F c.2630C>T 20 61525489 CM G A Missense p.S877F c.2630C>T 20 61525489 LUSC G A Missense p.S885L c.2654C>T 20 61525465 CM G A Missense p.T121I c.362C>T 20 61542603 CM G A Missense p.T26I c.77C>T 20 61542888 BRCA G A Missense p.T33I c.98C>T 20 61542867 LUAD G A Nonsense p.Q1540* c.4618C>T 20 61512690 ESCA G A Nonsense p.Q1540* c.4618C>T 20 61512690 HNSC G A Nonsense p.Q1965* c.5893C>T 20 61511415 BLCA G A Nonsense p.R1052* c.3154C>T 20 61524262 THCA G A Nonsense p.R30* c.88C>T 20 61542877 CM G A Synonymous p.A1858A c.5574C>T 20 61511734 HNSC G A Synonymous p.D1352D c.4056C>T 20 61513252 OV G A Synonymous p.F590F c.1770C>T 20 61528167 CM G A Synonymous p.G294G c.882C>T 20 61541330 LUAD G A Synonymous p.L1444L c.4330C>T 20 61512978 BLCA G A Synonymous p.L851L c.2553C>T 20 61525784 LUSC G A Synonymous p.P1748P c.5244C>T 20 61512064 CM G A Synonymous p.P1848P c.5544C>T 20 61511764 CM G A Synonymous p.P1867P c.5601C>T 20 61511707 STAD G A Synonymous p.P2025P c.6075C>T 20 61511233 CM G A Synonymous p.S1456S c.4368C>T 20 61512940 CM G A Synonymous p.S1471S c.4413C>T 20 61512895 LUSC G A Synonymous p.S1713S c.5139C>T 20 61512169 UCEC G A Synonymous p.S203S c.609C>T 20 61542356 CM G A Synonymous p.S952S c.2856C>T 20 61525263 CM G A Synonymous p.S964S c.2892C>T 20 61525227 CM G A Synonymous p.S964S c.2892C>T 20 61525227 PRAD G A Synonymous p.T151T c.453C>T 20 61542512 COREAD G A Synonymous p.T959T c.2877C>T 20 61525242 PRAD G A Synonymous p.V832V c.2496C>T 20 61525841 BLCA G A Synonymous p.Y721Y c.2163C>T 20 61527636 RCCC GC AT Missense p.A919I c.2755_2756delinsAT 20 61525363 COREAD G C Missense p.D1250E c.3750C>G 20 61513558 SCLC G C Missense p.P1673A c.5017C>G 20 61512291 CM G C Missense p.P1780R c.5339C>G 20 61511969 CM G C Missense p.P2059A c.6175C>G 20 61511133 OV G C Missense p.P2224R c.6671C>G 20 61510637 HNSC G C Missense p.Q1747E c.5239C>G 20 61512069 BRCA G C Missense p.Q1747E c.5239C>G 20 61512069 LUSC G C Missense p.R720G c.2158C>G 20 61527641 CM G C Synonymous p.L1500L c.4500C>G 20 61512808 BRCA GCTGCTGTTGTG - InFrameDeletion p.T1291_A1294delTTAA c.3870_3881delCACAACAGCAGC 20 61513427 RCCC G - Frameshift p.P1266Lfs*8 c.3797delC 20 61513511 STAD G - Frameshift p.P2034Rfs*213 c.6101delC 20 61511207 STAD GG AA Missense p.P869L c.2605_2606delinsTT 20 61525513 CM G T Missense p.P1029Q c.3086C>A 20 61525033 LUAD G T Missense p.P1625H c.4874C>A 20 61512434 CM G T Missense p.P2099Q c.6296C>A 20 61511012 STAD G T Missense p.P968H c.2903C>A 20 61525216 BRCA G T Missense p.S1809Y c.5426C>A 20 61511882 BLCA G T Nonsense p.S1764* c.5291C>A 20 61512017 LUSC G T Synonymous p.R1217R c.3649C>A 20 61513659 LUAD T A Missense p.H1849L c.5546A>T 20 61511762 LUSC T A Synonymous p.S609S c.1827A>T 20 61528110 LUAD T C Missense p.D147G c.440A>G 20 61542525 CM T C Missense p.H1557R c.4670A>G 20 61512638 HNSC T C Missense p.I315V c.943A>G 20 61541269 STAD T C Missense p.I702V c.2104A>G 20 61527695 LUSC T C Missense p.N1770D c.5308A>G 20 61512000 CM T C Missense p.Q1236R c.3707A>G 20 61513601 PRAD T C Missense p.S489G c.1465A>G 20 61537362 LUSC - T Frameshift p.E476Rfs*15 c.1425dupA 20 61537402 THCA - T Frameshift p.N2002Kfs*2 c.6005dupA 20 61511304 STAD T G Missense p.E362D c.1086A>C 20 61541126 LUSC T G Missense p.K1484T c.4451A>C 20 61512857 CM T G Missense p.K2096N c.6288A>C 20 61511020 LUAD T G Synonymous p.P1524P c.4572A>C 20 61512736 BRCA T G Synonymous p.T580T c.1740A>C 20 61528197 HNSC TT GC Missense p.N1204A c.3610_3611delinsGC 20 61513697 OV